## ENSEMBL VARIANT EFFECT PREDICTOR v72 ## Output produced at 2013-07-01 17:30:46 ## Connected to homo_sapiens_otherfeatures_72_37 on ensembldb.ensembl.org ## Using cache in /nfs/1000g-work/G1K/work/laura/grc_bases_to_check//homo_sapiens/72 ## Using API version 72, DB version 72 ## sift version sift5.0.2 ## polyphen version 2.2.2 ## Extra column keys: ## CELL_TYPE : List of cell types and classifications for regulatory feature ## DISTANCE : Shortest distance from variant to transcript ## HIGH_INF_POS : A flag indicating if the variant falls in a high information position of the TFBP ## MOTIF_NAME : The source and identifier of a transcription factor binding profile (TFBP) aligned at this position ## MOTIF_POS : The relative position of the variation in the aligned TFBP ## MOTIF_SCORE_CHANGE : The difference in motif score of the reference and variant sequences for the TFBP ## PolyPhen : PolyPhen prediction ## SIFT : SIFT prediction #Uploaded_variation Location Allele Gene Feature Feature_type Consequence cDNA_position CDS_position Protein_position Amino_acids Codons Existing_variation Extra rs3131984 1:715348 G - ENSR00001037663 RegulatoryFeature regulatory_region_variant - - - - - - rs3131984 1:715348 G ENSESTG00000013830 ENSESTT00000034563 Transcript upstream_gene_variant - - - - - - DISTANCE=1355 rs3131984 1:715348 G ENSESTG00000013594 ENSESTT00000034008 Transcript intron_variant - - - - - - rs3131984 1:715348 G ENSESTG00000013594 ENSESTT00000034004 Transcript intron_variant - - - - - - rs3131984 1:715348 G 100288069 NR_033908.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1280 rs3131943 1:770568 G 643837 NR_047524.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3131943 1:770568 G 643837 NR_047519.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3131943 1:770568 G 643837 NR_047521.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3131943 1:770568 G ENSESTG00000013607 ENSESTT00000034037 Transcript intron_variant - - - - - - rs3131943 1:770568 G 643837 NR_047525.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3131943 1:770568 G 643837 NR_047526.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3131943 1:770568 G ENSESTG00000013604 ENSESTT00000034028 Transcript intron_variant - - - - - - rs3131943 1:770568 G 643837 NR_047522.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3131943 1:770568 G 643837 NR_047523.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3131943 1:770568 G 643837 NR_047520.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3131943 1:770568 G 643837 NR_015368.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs10751454 1:807512 G 284593 NR_027055.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10751454 1:807512 G ENSESTG00000013818 ENSESTT00000034529 Transcript intron_variant - - - - - - rs4951932 1:807761 A 284593 NR_027055.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4951932 1:807761 A ENSESTG00000013818 ENSESTT00000034529 Transcript intron_variant - - - - - - rs4970378 1:883625 G CCDS2.2 CCDS2.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4092 rs4970378 1:883625 G CCDS3.1 CCDS3.1 Transcript intron_variant - - - - - - rs4970378 1:883625 G ENSESTG00000013767 ENSESTT00000034432 Transcript intron_variant - - - - - - rs4970378 1:883625 G ENSESTG00000013623 ENSESTT00000034116 Transcript downstream_gene_variant - - - - - - DISTANCE=3671 rs4970378 1:883625 G 26155 NM_015658.3 Transcript intron_variant - - - - - - rs4970378 1:883625 G ENSESTG00000013623 ENSESTT00000034117 Transcript downstream_gene_variant - - - - - - DISTANCE=4147 rs4970378 1:883625 G ENSESTG00000013795 ENSESTT00000034519 Transcript intron_variant - - - - - - rs4970378 1:883625 G 148398 NM_152486.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3664 rs6659787 1:1196863 C - ENSR00000528949 RegulatoryFeature regulatory_region_variant - - - - - - rs6659787 1:1196863 C CCDS14.1 CCDS14.1 Transcript intron_variant - - - - - - rs6659787 1:1196863 C ENSESTG00000033307 ENSESTT00000084189 Transcript intron_variant - - - - - - rs6659787 1:1196863 C 118424 NM_194315.1 Transcript intron_variant - - - - - - rs6659787 1:1196863 C ENSESTG00000033307 ENSESTT00000084200 Transcript intron_variant - - - - - - rs6659787 1:1196863 C 118424 NM_194457.1 Transcript intron_variant - - - - - - rs6659787 1:1196863 C ENSESTG00000033307 ENSESTT00000084242 Transcript intron_variant - - - - - - rs6659787 1:1196863 C CCDS15.1 CCDS15.1 Transcript intron_variant - - - - - - rs6659787 1:1196863 C ENSESTG00000033307 ENSESTT00000084205 Transcript intron_variant - - - - - - rs6659787 1:1196863 C CCDS16.1 CCDS16.1 Transcript intron_variant - - - - - - rs6659787 1:1196863 C 118424 NM_194458.1 Transcript intron_variant - - - - - - rs6659787 1:1196863 C ENSESTG00000033307 ENSESTT00000084239 Transcript intron_variant - - - - - - rs6659787 1:1196863 C ENSESTG00000033307 ENSESTT00000084234 Transcript intron_variant - - - - - - rs6659787 1:1196863 C 118424 NM_058167.2 Transcript intron_variant - - - - - - rs307360 1:1279025 G ENSESTG00000033174 ENSESTT00000083852 Transcript intron_variant - - - - - - rs307360 1:1279025 G CCDS22.1 CCDS22.1 Transcript intron_variant - - - - - - rs307360 1:1279025 G ENSESTG00000033174 ENSESTT00000083868 Transcript intron_variant - - - - - - rs307360 1:1279025 G 1855 NM_004421.2 Transcript intron_variant - - - - - - rs307360 1:1279025 G ENSESTG00000033174 ENSESTT00000083872 Transcript intron_variant - - - - - - rs307360 1:1279025 G ENSESTG00000033174 ENSESTT00000083880 Transcript intron_variant - - - - - - rs307360 1:1279025 G ENSESTG00000033174 ENSESTT00000083829 Transcript intron_variant - - - - - - rs1781144 1:1387667 G 219293 NM_001039211.2 Transcript intron_variant - - - - - - rs1781144 1:1387667 G ENSESTG00000032213 ENSESTT00000081411 Transcript upstream_gene_variant - - - - - - DISTANCE=4003 rs1781144 1:1387667 G ENSESTG00000032213 ENSESTT00000081392 Transcript upstream_gene_variant - - - - - - DISTANCE=3930 rs1781144 1:1387667 G ENSESTG00000032213 ENSESTT00000081287 Transcript upstream_gene_variant - - - - - - DISTANCE=3547 rs1781144 1:1387667 G ENSESTG00000032213 ENSESTT00000081318 Transcript upstream_gene_variant - - - - - - DISTANCE=3609 rs1781144 1:1387667 G CCDS44039.1 CCDS44039.1 Transcript intron_variant - - - - - - rs1781144 1:1387667 G ENSESTG00000032213 ENSESTT00000081407 Transcript upstream_gene_variant - - - - - - DISTANCE=3980 rs6603795 1:1744107 C CCDS34.1 CCDS34.1 Transcript intron_variant - - - - - - rs6603795 1:1744107 C ENSESTG00000032695 ENSESTT00000082819 Transcript intron_variant - - - - - - rs6603795 1:1744107 C 2782 NM_002074.3 Transcript intron_variant - - - - - - rs10909995 1:2779159 G - - - intergenic_variant - - - - - - rs2817142 1:3120201 C 63976 NM_199454.2 Transcript intron_variant - - - - - - rs2817142 1:3120201 C ENSESTG00000031798 ENSESTT00000080257 Transcript intron_variant - - - - - - rs2817142 1:3120201 C CCDS44048.2 CCDS44048.2 Transcript intron_variant - - - - - - rs2817142 1:3120201 C 63976 NM_022114.3 Transcript intron_variant - - - - - - rs2817142 1:3120201 C CCDS41236.2 CCDS41236.2 Transcript intron_variant - - - - - - rs2651921 1:3148079 C 63976 NM_199454.2 Transcript intron_variant - - - - - - rs2651921 1:3148079 C ENSESTG00000031798 ENSESTT00000080257 Transcript intron_variant - - - - - - rs2651921 1:3148079 C CCDS44048.2 CCDS44048.2 Transcript intron_variant - - - - - - rs2651921 1:3148079 C 63976 NM_022114.3 Transcript intron_variant - - - - - - rs2651921 1:3148079 C CCDS41236.2 CCDS41236.2 Transcript intron_variant - - - - - - rs2500307 1:3189732 A ENSESTG00000002830 ENSESTT00000007006 Transcript intron_variant - - - - - - rs2500307 1:3189732 A 63976 NM_199454.2 Transcript intron_variant - - - - - - rs2500307 1:3189732 A ENSESTG00000031798 ENSESTT00000080257 Transcript intron_variant - - - - - - rs2500307 1:3189732 A CCDS44048.2 CCDS44048.2 Transcript intron_variant - - - - - - rs2500307 1:3189732 A 63976 NM_022114.3 Transcript intron_variant - - - - - - rs2500307 1:3189732 A CCDS41236.2 CCDS41236.2 Transcript intron_variant - - - - - - rs2483231 1:3339071 G 63976 NM_199454.2 Transcript intron_variant - - - - - - rs2483231 1:3339071 G ENSESTG00000002862 ENSESTT00000007137 Transcript intron_variant - - - - - - rs2483231 1:3339071 G ENSESTG00000002862 ENSESTT00000007142 Transcript upstream_gene_variant - - - - - - DISTANCE=2414 rs2483231 1:3339071 G CCDS44048.2 CCDS44048.2 Transcript intron_variant - - - - - - rs2483231 1:3339071 G 63976 NM_022114.3 Transcript intron_variant - - - - - - rs2483231 1:3339071 G ENSESTG00000002862 ENSESTT00000007143 Transcript upstream_gene_variant - - - - - - DISTANCE=2709 rs2483231 1:3339071 G CCDS41236.2 CCDS41236.2 Transcript intron_variant - - - - - - rs2493313 1:3450255 C - ENSR00000529424 RegulatoryFeature regulatory_region_variant - - - - - - rs2493313 1:3450255 C 1953 NM_001409.3 Transcript intron_variant - - - - - - rs2493313 1:3450255 C CCDS41237.1 CCDS41237.1 Transcript intron_variant - - - - - - rs2821014 1:3518857 C 1953 NM_001409.3 Transcript intron_variant - - - - - - rs2821014 1:3518857 C CCDS41237.1 CCDS41237.1 Transcript intron_variant - - - - - - rs2821014 1:3518857 C ENSESTG00000004147 ENSESTT00000010461 Transcript downstream_gene_variant - - - - - - DISTANCE=247 rs6695126 1:4210204 G - - - intergenic_variant - - - - - - rs4336820 1:4216770 C - - - intergenic_variant - - - - - - rs12062237 1:4217290 C - - - intergenic_variant - - - - - - rs4654498 1:4228312 G - - - intergenic_variant - - - - - - rs349395 1:4418243 G - - - intergenic_variant - - - - - - rs780603 1:4557403 C - - - intergenic_variant - - - - - - rs1762828 1:4573467 A - - - intergenic_variant - - - - - - rs241213 1:4650780 A - - - intergenic_variant - - - - - - rs241242 1:4668157 T - - - intergenic_variant - - - - - - rs2746060 1:6186961 G - ENSR00000162997 RegulatoryFeature regulatory_region_variant - - - - - - rs2746060 1:6186961 G CCDS57.1 CCDS57.1 Transcript intron_variant - - - - - - rs2746060 1:6186961 G ENSESTG00000023369 ENSESTT00000058930 Transcript upstream_gene_variant - - - - - - DISTANCE=2880 rs2746060 1:6186961 G ENSESTG00000023320 ENSESTT00000058882 Transcript intron_variant - - - - - - rs2746060 1:6186961 G 26038 NM_015557.2 Transcript intron_variant - - - - - - rs2898916 1:7091542 G CCDS30576.1 CCDS30576.1 Transcript intron_variant - - - - - - rs2898916 1:7091542 G 23261 NM_015215.2 Transcript intron_variant - - - - - - rs1008216 1:7293471 G CCDS30576.1 CCDS30576.1 Transcript intron_variant - - - - - - rs1008216 1:7293471 G 23261 NM_015215.2 Transcript intron_variant - - - - - - rs763169 1:7400072 G CCDS30576.1 CCDS30576.1 Transcript intron_variant - - - - - - rs763169 1:7400072 G 23261 NM_015215.2 Transcript intron_variant - - - - - - rs763171 1:7400200 G - ENSR00000529855 RegulatoryFeature regulatory_region_variant - - - - - - rs763171 1:7400200 G CCDS30576.1 CCDS30576.1 Transcript intron_variant - - - - - - rs763171 1:7400200 G 23261 NM_015215.2 Transcript intron_variant - - - - - - rs2859319 1:7490439 A CCDS30576.1 CCDS30576.1 Transcript intron_variant - - - - - - rs2859319 1:7490439 A 23261 NM_015215.2 Transcript intron_variant - - - - - - rs11120925 1:7490618 G CCDS30576.1 CCDS30576.1 Transcript intron_variant - - - - - - rs11120925 1:7490618 G 23261 NM_015215.2 Transcript intron_variant - - - - - - rs707456 1:7829226 G ENSESTG00000004874 ENSESTT00000012413 Transcript upstream_gene_variant - - - - - - DISTANCE=2139 rs707456 1:7829226 G 9341 NM_004781.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2103 rs707456 1:7829226 G ENSESTG00000004926 ENSESTT00000012522 Transcript intron_variant - - - - - - rs707456 1:7829226 G ENSESTG00000004866 ENSESTT00000012338 Transcript downstream_gene_variant - - - - - - DISTANCE=2366 rs707456 1:7829226 G 23261 NM_015215.2 Transcript 3_prime_UTR_variant 7904 - - - - - rs707456 1:7829226 G ENSESTG00000004874 ENSESTT00000012420 Transcript upstream_gene_variant - - - - - - DISTANCE=2453 rs707456 1:7829226 G ENSESTG00000004874 ENSESTT00000012389 Transcript upstream_gene_variant - - - - - - DISTANCE=2109 rs707456 1:7829226 G ENSESTG00000004938 ENSESTT00000012555 Transcript downstream_gene_variant - - - - - - DISTANCE=2168 rs707456 1:7829226 G ENSESTG00000004874 ENSESTT00000012384 Transcript upstream_gene_variant - - - - - - DISTANCE=2109 rs707456 1:7829226 G ENSESTG00000004874 ENSESTT00000012410 Transcript upstream_gene_variant - - - - - - DISTANCE=2139 rs707456 1:7829226 G ENSESTG00000004866 ENSESTT00000012345 Transcript downstream_gene_variant - - - - - - DISTANCE=2403 rs707456 1:7829226 G ENSESTG00000004866 ENSESTT00000012344 Transcript downstream_gene_variant - - - - - - DISTANCE=2366 rs707456 1:7829226 G CCDS88.1 CCDS88.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2218 rs707456 1:7829226 G ENSESTG00000004874 ENSESTT00000012391 Transcript upstream_gene_variant - - - - - - DISTANCE=2109 rs707456 1:7829226 G ENSESTG00000004866 ENSESTT00000012342 Transcript downstream_gene_variant - - - - - - DISTANCE=2403 rs707456 1:7829226 G CCDS30576.1 CCDS30576.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2675 rs6680788 1:8151242 C - ENSR00000668788 RegulatoryFeature regulatory_region_variant - - - - - - rs6680788 1:8151242 C - - - intergenic_variant - - - - - - rs10746476 1:8176768 A - ENSR00001517140 RegulatoryFeature regulatory_region_variant - - - - - - rs10746476 1:8176768 A - - - intergenic_variant - - - - - - rs299489 1:8318082 C - ENSR00000668793 RegulatoryFeature regulatory_region_variant - - - - - - rs299489 1:8318082 C - - - intergenic_variant - - - - - - rs301787 1:8472837 T - ENSR00000530042 RegulatoryFeature regulatory_region_variant - - - - - - rs301787 1:8472837 T ENSESTG00000012337 ENSESTT00000030968 Transcript intron_variant - - - - - - rs301787 1:8472837 T 473 NM_001042681.1 Transcript intron_variant - - - - - - rs301787 1:8472837 T 473 NM_012102.3 Transcript intron_variant - - - - - - rs301787 1:8472837 T ENSESTG00000012337 ENSESTT00000030976 Transcript intron_variant - - - - - - rs301787 1:8472837 T 473 NM_001042682.1 Transcript intron_variant - - - - - - rs301787 1:8472837 T ENSESTG00000012337 ENSESTT00000030982 Transcript intron_variant - - - - - - rs301787 1:8472837 T CCDS95.1 CCDS95.1 Transcript intron_variant - - - - - - rs301787 1:8472837 T ENSESTG00000012337 ENSESTT00000030955 Transcript intron_variant - - - - - - rs301787 1:8472837 T ENSESTG00000012337 ENSESTT00000030960 Transcript intron_variant - - - - - - rs6577487 1:8527630 A CCDS95.1 CCDS95.1 Transcript intron_variant - - - - - - rs6577487 1:8527630 A 473 NM_001042681.1 Transcript intron_variant - - - - - - rs6577487 1:8527630 A 473 NM_012102.3 Transcript intron_variant - - - - - - rs6577487 1:8527630 A ENSESTG00000012237 ENSESTT00000030615 Transcript intron_variant - - - - - - rs6577487 1:8527630 A ENSESTG00000012337 ENSESTT00000030955 Transcript upstream_gene_variant - - - - - - DISTANCE=1586 rs2781084 1:8995653 A - - - intergenic_variant - - - - - - rs1705303 1:9165868 G 80045 NM_024980.4 Transcript intron_variant - - - - - - rs1705303 1:9165868 G CCDS100.2 CCDS100.2 Transcript intron_variant - - - - - - rs6605052 1:9477924 A - ENSR00000163218 RegulatoryFeature regulatory_region_variant - - - - - - rs6605052 1:9477924 A - - - intergenic_variant - - - - - - rs6605050 1:9485706 C - - - intergenic_variant - - - - - - rs284275 1:10651912 C ENSESTG00000012857 ENSESTT00000032275 Transcript intron_variant - - - - - - rs284275 1:10651912 C ENSESTG00000012857 ENSESTT00000032267 Transcript intron_variant - - - - - - rs284275 1:10651912 C 5195 NM_004565.2 Transcript intron_variant - - - - - - rs284275 1:10651912 C CCDS30582.1 CCDS30582.1 Transcript intron_variant - - - - - - rs284275 1:10651912 C ENSESTG00000012857 ENSESTT00000032280 Transcript intron_variant - - - - - - rs284275 1:10651912 C ENSESTG00000012857 ENSESTT00000032272 Transcript intron_variant - - - - - - rs284318 1:10731598 G CCDS41246.1 CCDS41246.1 Transcript intron_variant - - - - - - rs284318 1:10731598 G 54897 NM_017766.3 Transcript intron_variant - - - - - - rs284318 1:10731598 G ENSESTG00000012905 ENSESTT00000032366 Transcript intron_variant - - - - - - rs284318 1:10731598 G 54897 NM_001079843.1 Transcript intron_variant - - - - - - rs284318 1:10731598 G ENSESTG00000012905 ENSESTT00000032362 Transcript intron_variant - - - - - - rs284318 1:10731598 G ENSESTG00000012905 ENSESTT00000032368 Transcript intron_variant - - - - - - rs284318 1:10731598 G CCDS120.2 CCDS120.2 Transcript intron_variant - - - - - - rs58243167 1:11101252 G 10747 NM_006610.3 Transcript intron_variant - - - - - - rs58243167 1:11101252 G 10747 NM_139208.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3603 rs58243167 1:11101252 G ENSESTG00000008208 ENSESTT00000020742 Transcript intron_variant - - - - - - rs58243167 1:11101252 G CCDS123.1 CCDS123.1 Transcript intron_variant - - - - - - rs58243167 1:11101252 G CCDS124.1 CCDS124.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3745 rs58243167 1:11101252 G ENSESTG00000007209 ENSESTT00000018195 Transcript downstream_gene_variant - - - - - - DISTANCE=3207 rs58243167 1:11101252 G ENSESTG00000012902 ENSESTT00000032351 Transcript intron_variant - - - - - - rs2335397 1:11267750 T ENSESTG00000007920 ENSESTT00000020073 Transcript intron_variant - - - - - - rs2335397 1:11267750 T CCDS127.1 CCDS127.1 Transcript intron_variant - - - - - - rs2335397 1:11267750 T ENSESTG00000007920 ENSESTT00000020067 Transcript intron_variant - - - - - - rs2335397 1:11267750 T 2475 NM_004958.3 Transcript intron_variant - - - - - - rs3117070 1:11691686 C - - - intergenic_variant - - - - - - rs4845885 1:11858672 C - ENSR00000279228 RegulatoryFeature regulatory_region_variant - - - - - - rs4845885 1:11858672 C - MA0140.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=10;MOTIF_NAME=Jaspar_Matrix_Tal1::Gata1:MA0140.1;HIGH_INF_POS=N;MOTIF_SCORE_CHANGE=-0.001 rs4845885 1:11858672 C 4524 NM_005957.4 Transcript intron_variant - - - - - - rs4845885 1:11858672 C ENSESTG00000007786 ENSESTT00000019710 Transcript intron_variant - - - - - - rs4845885 1:11858672 C ENSESTG00000007786 ENSESTT00000019667 Transcript downstream_gene_variant - - - - - - DISTANCE=2718 rs4845885 1:11858672 C CCDS137.1 CCDS137.1 Transcript intron_variant - - - - - - rs4846087 1:12079257 C - ENSR00000279264 RegulatoryFeature regulatory_region_variant - - - - - - rs4846087 1:12079257 C ENSESTG00000004673 ENSESTT00000011841 Transcript upstream_gene_variant - - - - - - DISTANCE=3664 rs4846087 1:12079257 C ENSESTG00000004673 ENSESTT00000011789 Transcript upstream_gene_variant - - - - - - DISTANCE=270 rs4846087 1:12079257 C ENSESTG00000004673 ENSESTT00000011805 Transcript upstream_gene_variant - - - - - - DISTANCE=304 rs4846087 1:12079257 C ENSESTG00000004838 ENSESTT00000012268 Transcript downstream_gene_variant - - - - - - DISTANCE=2451 rs4846087 1:12079257 C ENSESTG00000004673 ENSESTT00000011835 Transcript upstream_gene_variant - - - - - - DISTANCE=3631 rs4846087 1:12079257 C 60672 NM_021933.3 Transcript upstream_gene_variant - - - - - - DISTANCE=42 rs4846087 1:12079257 C CCDS143.1 CCDS143.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2527 rs4846087 1:12079257 C ENSESTG00000004838 ENSESTT00000012266 Transcript downstream_gene_variant - - - - - - DISTANCE=2904 rs1763642 1:12175729 T CCDS144.1 CCDS144.1 Transcript missense_variant 889 889 297 R/C Cgt/Tgt - PolyPhen=benign;SIFT=tolerated rs1763642 1:12175729 T ENSESTG00000004700 ENSESTT00000011852 Transcript missense_variant 590 556 186 R/C Cgt/Tgt - rs1763642 1:12175729 T 943 NM_001243.3 Transcript missense_variant 1111 889 297 R/C Cgt/Tgt - PolyPhen=benign;SIFT=tolerated rs6682241 1:12467201 C ENSESTG00000004755 ENSESTT00000012128 Transcript intron_variant - - - - - - rs6682241 1:12467201 C ENSESTG00000004755 ENSESTT00000012125 Transcript intron_variant - - - - - - rs6682241 1:12467201 C 55187 NM_015378.2 Transcript intron_variant - - - - - - rs6682241 1:12467201 C 55187 NM_018156.2 Transcript intron_variant - - - - - - rs6682241 1:12467201 C ENSESTG00000004755 ENSESTT00000012123 Transcript intron_variant - - - - - - rs6682241 1:12467201 C CCDS30588.1 CCDS30588.1 Transcript intron_variant - - - - - - rs6682241 1:12467201 C CCDS30589.1 CCDS30589.1 Transcript intron_variant - - - - - - rs6682241 1:12467201 C ENSESTG00000004755 ENSESTT00000012107 Transcript intron_variant - - - - - - rs6682241 1:12467201 C ENSESTG00000004755 ENSESTT00000012109 Transcript intron_variant - - - - - - rs6682241 1:12467201 C ENSESTG00000004755 ENSESTT00000012119 Transcript intron_variant - - - - - - rs7512533 1:12633405 G CCDS146.1 CCDS146.1 Transcript intron_variant - - - - - - rs7512533 1:12633405 G ENSESTG00000004816 ENSESTT00000012254 Transcript intron_variant - - - - - - rs7512533 1:12633405 G ENSESTG00000004816 ENSESTT00000012242 Transcript intron_variant - - - - - - rs7512533 1:12633405 G 9249 NM_004753.4 Transcript intron_variant - - - - - - rs354587 1:13819969 G 126755 NM_001010847.1 Transcript intron_variant - - - - - - rs354587 1:13819969 G CCDS53269.1 CCDS53269.1 Transcript intron_variant - - - - - - rs354587 1:13819969 G ENSESTG00000013436 ENSESTT00000033627 Transcript intron_variant - - - - - - rs2697993 1:14237101 C - - - intergenic_variant - - - - - - rs6699506 1:14436717 C - - - intergenic_variant - - - - - - rs1416629 1:14597782 G - - - intergenic_variant - - - - - - rs7538477 1:14788938 C - - - intergenic_variant - - - - - - rs7545212 1:14793635 A - - - intergenic_variant - - - - - - rs2819550 1:15782027 G ENSESTG00000012338 ENSESTT00000030998 Transcript upstream_gene_variant - - - - - - DISTANCE=1200 rs2819550 1:15782027 G 63036 NM_033440.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1196 rs2819550 1:15782027 G ENSESTG00000012338 ENSESTT00000030971 Transcript upstream_gene_variant - - - - - - DISTANCE=1196 rs2819550 1:15782027 G ENSESTG00000012338 ENSESTT00000031001 Transcript upstream_gene_variant - - - - - - DISTANCE=1227 rs2819550 1:15782027 G CCDS157.1 CCDS157.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1222 rs2819550 1:15782027 G ENSESTG00000012338 ENSESTT00000031007 Transcript upstream_gene_variant - - - - - - DISTANCE=1562 rs2011159 1:15813751 T ENSESTG00000012338 ENSESTT00000031030 Transcript intron_variant - - - - - - rs2011159 1:15813751 T CCDS30605.1 CCDS30605.1 Transcript intron_variant - - - - - - rs2011159 1:15813751 T 51032 NM_015849.2 Transcript intron_variant - - - - - - rs2011159 1:15813751 T ENSESTG00000012338 ENSESTT00000031007 Transcript downstream_gene_variant - - - - - - DISTANCE=3861 rs2753289 1:15881153 T ENSESTG00000012398 ENSESTT00000031100 Transcript intron_variant - - - - - - rs2753289 1:15881153 T ENSESTG00000012398 ENSESTT00000031095 Transcript intron_variant - - - - - - rs2753289 1:15881153 T 23341 NM_015291.2 Transcript intron_variant - - - - - - rs2753289 1:15881153 T CCDS30606.1 CCDS30606.1 Transcript intron_variant - - - - - - rs2009044 1:16362621 A CCDS57973.1 CCDS57973.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2468 rs2009044 1:16362621 A CCDS167.1 CCDS167.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2468 rs2009044 1:16362621 A 1187 NM_001257139.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2076 rs2009044 1:16362621 A ENSESTG00000014918 ENSESTT00000037385 Transcript downstream_gene_variant - - - - - - DISTANCE=3007 rs2009044 1:16362621 A ENSESTG00000022028 ENSESTT00000055509 Transcript downstream_gene_variant - - - - - - DISTANCE=3844 rs2009044 1:16362621 A CCDS41269.1 CCDS41269.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2468 rs2009044 1:16362621 A ENSESTG00000021906 ENSESTT00000055330 Transcript intron_variant - - - - - - rs2009044 1:16362621 A ENSESTG00000022059 ENSESTT00000055544 Transcript downstream_gene_variant - - - - - - DISTANCE=2166 rs2009044 1:16362621 A 1187 NM_001042704.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2076 rs2009044 1:16362621 A ENSESTG00000021906 ENSESTT00000055234 Transcript intron_variant - - - - - - rs2009044 1:16362621 A 1187 NM_004070.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2076 rs6678720 1:16502623 C - ENSR00000531307 RegulatoryFeature regulatory_region_variant - - - - - - rs6678720 1:16502623 C - - - intergenic_variant - - - - - - rs6586566 1:17248532 G - ENSR00000531485 RegulatoryFeature regulatory_region_variant - - - - - - rs6586566 1:17248532 G 9696 NM_014675.3 Transcript missense_variant 88 19 7 R/G Agg/Ggg - PolyPhen=unknown;SIFT=tolerated rs6586566 1:17248532 G CCDS30616.1 CCDS30616.1 Transcript missense_variant 19 19 7 R/G Agg/Ggg - PolyPhen=unknown;SIFT=tolerated rs2647177 1:17448611 C - ENSR00001517818 RegulatoryFeature regulatory_region_variant - - - - - - rs2647177 1:17448611 C 11240 NM_007365.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2663 rs2647177 1:17448611 C ENSESTG00000025079 ENSESTT00000063474 Transcript upstream_gene_variant - - - - - - DISTANCE=2665 rs2647177 1:17448611 C CCDS177.1 CCDS177.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2745 rs2477738 1:17869550 C ENSESTG00000024623 ENSESTT00000062401 Transcript intron_variant - - - - - - rs2477738 1:17869550 C ENSESTG00000024623 ENSESTT00000062380 Transcript intron_variant - - - - - - rs2477738 1:17869550 C 55160 NM_018125.3 Transcript intron_variant - - - - - - rs2477738 1:17869550 C ENSESTG00000024623 ENSESTT00000062426 Transcript intron_variant - - - - - - rs6695710 1:17991052 C ENSESTG00000018546 ENSESTT00000046912 Transcript missense_variant 1532 919 307 W/R Tgg/Cgg - rs6695710 1:17991052 C ENSESTG00000018546 ENSESTT00000046908 Transcript intron_variant - - - - - - rs6695710 1:17991052 C ENSESTG00000018546 ENSESTT00000046906 Transcript intron_variant - - - - - - rs6695710 1:17991052 C ENSESTG00000018546 ENSESTT00000046857 Transcript missense_variant 1968 1918 640 W/R Tgg/Cgg - rs6695710 1:17991052 C CCDS182.1 CCDS182.1 Transcript missense_variant 2971 2971 991 W/R Tgg/Cgg - PolyPhen=benign;SIFT=tolerated rs6695710 1:17991052 C ENSESTG00000018546 ENSESTT00000046752 Transcript intron_variant - - - - - - rs6695710 1:17991052 C CCDS30617.1 CCDS30617.1 Transcript missense_variant 2854 2854 952 W/R Tgg/Cgg - PolyPhen=benign;SIFT=tolerated rs6695710 1:17991052 C ENSESTG00000018546 ENSESTT00000046769 Transcript intron_variant - - - - - - rs6695710 1:17991052 C 55160 NM_018125.3 Transcript missense_variant 3130 2971 991 W/R Tgg/Cgg - PolyPhen=benign;SIFT=tolerated rs6695710 1:17991052 C 55160 NM_001011722.2 Transcript missense_variant 2897 2854 952 W/R Tgg/Cgg - PolyPhen=benign;SIFT=tolerated rs6694242 1:18028612 G ENSESTG00000018735 ENSESTT00000047210 Transcript upstream_gene_variant - - - - - - DISTANCE=4248 rs6694242 1:18028612 G ENSESTG00000018546 ENSESTT00000046908 Transcript downstream_gene_variant - - - - - - DISTANCE=4249 rs6694242 1:18028612 G ENSESTG00000018546 ENSESTT00000046906 Transcript downstream_gene_variant - - - - - - DISTANCE=4249 rs6694242 1:18028612 G CCDS182.1 CCDS182.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4737 rs6694242 1:18028612 G ENSESTG00000018546 ENSESTT00000046752 Transcript downstream_gene_variant - - - - - - DISTANCE=4249 rs6694242 1:18028612 G CCDS30617.1 CCDS30617.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4737 rs6694242 1:18028612 G ENSESTG00000018546 ENSESTT00000046769 Transcript downstream_gene_variant - - - - - - DISTANCE=4249 rs6694242 1:18028612 G 55160 NM_018125.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4242 rs6694242 1:18028612 G 55160 NM_001011722.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4242 rs1934031 1:18346588 G - - - intergenic_variant - - - - - - rs946375 1:18364428 G - - - intergenic_variant - - - - - - rs9662970 1:18404792 T - - - intergenic_variant - - - - - - rs170341 1:18598838 G 84966 NM_032880.4 Transcript intron_variant - - - - - - rs170341 1:18598838 G ENSESTG00000018668 ENSESTT00000047114 Transcript intron_variant - - - - - - rs170341 1:18598838 G CCDS184.1 CCDS184.1 Transcript intron_variant - - - - - - rs170341 1:18598838 G ENSESTG00000018668 ENSESTT00000047122 Transcript intron_variant - - - - - - rs170341 1:18598838 G ENSESTG00000018668 ENSESTT00000047094 Transcript intron_variant - - - - - - rs170341 1:18598838 G ENSESTG00000018668 ENSESTT00000047137 Transcript intron_variant - - - - - - rs223155 1:18628488 G 84966 NM_032880.4 Transcript intron_variant - - - - - - rs223155 1:18628488 G ENSESTG00000018668 ENSESTT00000047114 Transcript intron_variant - - - - - - rs223155 1:18628488 G CCDS184.1 CCDS184.1 Transcript intron_variant - - - - - - rs223155 1:18628488 G ENSESTG00000018668 ENSESTT00000047122 Transcript intron_variant - - - - - - rs223155 1:18628488 G ENSESTG00000018668 ENSESTT00000047094 Transcript intron_variant - - - - - - rs223155 1:18628488 G ENSESTG00000018668 ENSESTT00000047137 Transcript intron_variant - - - - - - rs223156 1:18628554 C 84966 NM_032880.4 Transcript intron_variant - - - - - - rs223156 1:18628554 C ENSESTG00000018668 ENSESTT00000047114 Transcript intron_variant - - - - - - rs223156 1:18628554 C CCDS184.1 CCDS184.1 Transcript intron_variant - - - - - - rs223156 1:18628554 C ENSESTG00000018668 ENSESTT00000047122 Transcript intron_variant - - - - - - rs223156 1:18628554 C ENSESTG00000018668 ENSESTT00000047094 Transcript intron_variant - - - - - - rs223156 1:18628554 C ENSESTG00000018668 ENSESTT00000047137 Transcript intron_variant - - - - - - rs223169 1:18654055 G 84966 NM_032880.4 Transcript intron_variant - - - - - - rs223169 1:18654055 G ENSESTG00000018668 ENSESTT00000047114 Transcript intron_variant - - - - - - rs223169 1:18654055 G CCDS184.1 CCDS184.1 Transcript intron_variant - - - - - - rs223169 1:18654055 G ENSESTG00000018668 ENSESTT00000047122 Transcript intron_variant - - - - - - rs223169 1:18654055 G ENSESTG00000018668 ENSESTT00000047094 Transcript intron_variant - - - - - - rs223169 1:18654055 G ENSESTG00000018668 ENSESTT00000047137 Transcript intron_variant - - - - - - rs1739102 1:18683943 G 84966 NM_032880.4 Transcript intron_variant - - - - - - rs1739102 1:18683943 G ENSESTG00000018668 ENSESTT00000047114 Transcript intron_variant - - - - - - rs1739102 1:18683943 G CCDS184.1 CCDS184.1 Transcript intron_variant - - - - - - rs1739102 1:18683943 G ENSESTG00000018668 ENSESTT00000047094 Transcript intron_variant - - - - - - rs1739103 1:18684185 G 84966 NM_032880.4 Transcript intron_variant - - - - - - rs1739103 1:18684185 G ENSESTG00000018668 ENSESTT00000047114 Transcript intron_variant - - - - - - rs1739103 1:18684185 G CCDS184.1 CCDS184.1 Transcript intron_variant - - - - - - rs1739103 1:18684185 G ENSESTG00000018668 ENSESTT00000047094 Transcript intron_variant - - - - - - rs4333871 1:19257998 T ENSESTG00000010027 ENSESTT00000025090 Transcript intron_variant - - - - - - rs4333871 1:19257998 T 126917 NM_001136265.1 Transcript intron_variant - - - - - - rs4333871 1:19257998 T CCDS44076.1 CCDS44076.1 Transcript intron_variant - - - - - - rs4333871 1:19257998 T ENSESTG00000010027 ENSESTT00000025085 Transcript intron_variant - - - - - - rs2983108 1:19269281 A ENSESTG00000015569 ENSESTT00000038986 Transcript downstream_gene_variant - - - - - - DISTANCE=2840 rs2983108 1:19269281 A ENSESTG00000010027 ENSESTT00000025090 Transcript intron_variant - - - - - - rs2983108 1:19269281 A 126917 NM_001136265.1 Transcript intron_variant - - - - - - rs2983108 1:19269281 A CCDS44076.1 CCDS44076.1 Transcript intron_variant - - - - - - rs2983108 1:19269281 A ENSESTG00000010027 ENSESTT00000025085 Transcript intron_variant - - - - - - rs12031823 1:19617855 A 100506730 NR_037847.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1886 rs12031823 1:19617855 A ENSESTG00000009898 ENSESTT00000024784 Transcript upstream_gene_variant - - - - - - DISTANCE=2610 rs12031823 1:19617855 A 22977 NM_012067.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2575 rs12031823 1:19617855 A ENSESTG00000009898 ENSESTT00000024790 Transcript upstream_gene_variant - - - - - - DISTANCE=4991 rs12031823 1:19617855 A CCDS193.1 CCDS193.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2652 rs214300 1:19685458 C ENSESTG00000009834 ENSESTT00000024700 Transcript intron_variant - - - - - - rs214300 1:19685458 C CCDS41277.1 CCDS41277.1 Transcript intron_variant - - - - - - rs214300 1:19685458 C ENSESTG00000009834 ENSESTT00000024726 Transcript intron_variant - - - - - - rs214300 1:19685458 C 832 NR_038125.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs214300 1:19685458 C ENSESTG00000009834 ENSESTT00000024732 Transcript intron_variant - - - - - - rs214300 1:19685458 C 832 NM_001206540.1 Transcript intron_variant - - - - - - rs214300 1:19685458 C ENSESTG00000009834 ENSESTT00000024718 Transcript intron_variant - - - - - - rs214300 1:19685458 C ENSESTG00000009834 ENSESTT00000024724 Transcript intron_variant - - - - - - rs214300 1:19685458 C ENSESTG00000009834 ENSESTT00000024748 Transcript intron_variant - - - - - - rs214300 1:19685458 C CCDS55579.1 CCDS55579.1 Transcript intron_variant - - - - - - rs214300 1:19685458 C ENSESTG00000009834 ENSESTT00000024758 Transcript intron_variant - - - - - - rs214300 1:19685458 C ENSESTG00000009834 ENSESTT00000024688 Transcript intron_variant - - - - - - rs214300 1:19685458 C 832 NM_004930.3 Transcript intron_variant - - - - - - rs761072 1:20084582 C CCDS198.1 CCDS198.1 Transcript intron_variant - - - - - - rs761072 1:20084582 C 255104 NM_181719.4 Transcript intron_variant - - - - - - rs761072 1:20084582 C ENSESTG00000000227 ENSESTT00000000560 Transcript intron_variant - - - - - - rs761072 1:20084582 C ENSESTG00000000227 ENSESTT00000000566 Transcript intron_variant - - - - - - rs761072 1:20084582 C ENSESTG00000000227 ENSESTT00000000564 Transcript intron_variant - - - - - - rs761072 1:20084582 C ENSESTG00000000227 ENSESTT00000000558 Transcript intron_variant - - - - - - rs1266435 1:20098830 A - ENSR00001518016 RegulatoryFeature regulatory_region_variant - - - - - - rs1266435 1:20098830 A CCDS198.1 CCDS198.1 Transcript intron_variant - - - - - - rs1266435 1:20098830 A 255104 NM_181719.4 Transcript intron_variant - - - - - - rs1266435 1:20098830 A ENSESTG00000000227 ENSESTT00000000560 Transcript intron_variant - - - - - - rs1266435 1:20098830 A ENSESTG00000000227 ENSESTT00000000566 Transcript intron_variant - - - - - - rs1266435 1:20098830 A ENSESTG00000000227 ENSESTT00000000564 Transcript intron_variant - - - - - - rs1266435 1:20098830 A ENSESTG00000000227 ENSESTT00000000558 Transcript intron_variant - - - - - - rs4255355 1:20159588 A - - - intergenic_variant - - - - - - rs763204 1:20523874 G - ENSR00000279963 RegulatoryFeature regulatory_region_variant - - - - - - rs763204 1:20523874 G 127733 NM_152376.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3932 rs6426620 1:20539032 T - ENSR00000075276 RegulatoryFeature regulatory_region_variant - - - - - - rs6426620 1:20539032 T - - - intergenic_variant - - - - - - rs1152992 1:20902416 G - - - intergenic_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053166 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053097 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000052995 Transcript intron_variant - - - - - - rs645454 1:21590506 C 1889 NM_001113348.1 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020288 ENSESTT00000050882 Transcript upstream_gene_variant - - - - - - DISTANCE=2069 rs645454 1:21590506 C 1889 NM_001397.2 Transcript intron_variant - - - - - - rs645454 1:21590506 C CCDS44081.1 CCDS44081.1 Transcript intron_variant - - - - - - rs645454 1:21590506 C CCDS215.1 CCDS215.1 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053122 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053055 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053049 Transcript intron_variant - - - - - - rs645454 1:21590506 C 1889 NM_001113349.1 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053114 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053015 Transcript intron_variant - - - - - - rs645454 1:21590506 C CCDS44082.1 CCDS44082.1 Transcript intron_variant - - - - - - rs645454 1:21590506 C CCDS44083.1 CCDS44083.1 Transcript intron_variant - - - - - - rs645454 1:21590506 C 1889 NM_001113347.1 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053153 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053156 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053007 Transcript intron_variant - - - - - - rs645454 1:21590506 C ENSESTG00000020931 ENSESTT00000053062 Transcript intron_variant - - - - - - rs1772721 1:21905124 G 249 NM_001177520.1 Transcript downstream_gene_variant - - - - - - DISTANCE=219 rs1772721 1:21905124 G CCDS53274.1 CCDS53274.1 Transcript downstream_gene_variant - - - - - - DISTANCE=983 rs1772721 1:21905124 G ENSESTG00000020522 ENSESTT00000051667 Transcript downstream_gene_variant - - - - - - DISTANCE=833 rs1772721 1:21905124 G ENSESTG00000020522 ENSESTT00000051665 Transcript downstream_gene_variant - - - - - - DISTANCE=833 rs1772721 1:21905124 G ENSESTG00000020522 ENSESTT00000051577 Transcript downstream_gene_variant - - - - - - DISTANCE=225 rs1772721 1:21905124 G 249 NM_000478.4 Transcript downstream_gene_variant - - - - - - DISTANCE=219 rs1772721 1:21905124 G 249 NM_001127501.2 Transcript downstream_gene_variant - - - - - - DISTANCE=219 rs1772721 1:21905124 G CCDS53275.1 CCDS53275.1 Transcript downstream_gene_variant - - - - - - DISTANCE=983 rs1772721 1:21905124 G ENSESTG00000020522 ENSESTT00000051692 Transcript downstream_gene_variant - - - - - - DISTANCE=833 rs1772721 1:21905124 G CCDS217.1 CCDS217.1 Transcript downstream_gene_variant - - - - - - DISTANCE=983 rs2995002 1:21945990 G - ENSR00000532236 RegulatoryFeature regulatory_region_variant - - - - - - rs2995002 1:21945990 G ENSESTG00000014092 ENSESTT00000035298 Transcript intron_variant - - - - - - rs2995002 1:21945990 G CCDS53276.1 CCDS53276.1 Transcript intron_variant - - - - - - rs2995002 1:21945990 G ENSESTG00000014092 ENSESTT00000035302 Transcript intron_variant - - - - - - rs2995002 1:21945990 G CCDS218.1 CCDS218.1 Transcript intron_variant - - - - - - rs2995002 1:21945990 G 5909 NM_002885.2 Transcript intron_variant - - - - - - rs2995002 1:21945990 G 5909 NM_001145657.1 Transcript intron_variant - - - - - - rs2995002 1:21945990 G ENSESTG00000014092 ENSESTT00000035266 Transcript intron_variant - - - - - - rs2995002 1:21945990 G 5909 NM_001145658.1 Transcript intron_variant - - - - - - rs2995002 1:21945990 G ENSESTG00000014092 ENSESTT00000035289 Transcript intron_variant - - - - - - rs2995002 1:21945990 G CCDS53277.1 CCDS53277.1 Transcript intron_variant - - - - - - rs2995002 1:21945990 G ENSESTG00000014092 ENSESTT00000035306 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035193 Transcript intron_variant - - - - - - rs333183 1:22059515 A 84196 NM_032236.5 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035166 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035161 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035190 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035198 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035195 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035201 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035148 Transcript intron_variant - - - - - - rs333183 1:22059515 A CCDS44084.1 CCDS44084.1 Transcript intron_variant - - - - - - rs333183 1:22059515 A CCDS30623.1 CCDS30623.1 Transcript intron_variant - - - - - - rs333183 1:22059515 A 84196 NM_001032730.1 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035173 Transcript intron_variant - - - - - - rs333183 1:22059515 A ENSESTG00000014024 ENSESTT00000035183 Transcript intron_variant - - - - - - rs664340 1:22925292 G 2046 NM_020526.3 Transcript intron_variant - - - - - - rs664340 1:22925292 G CCDS225.1 CCDS225.1 Transcript intron_variant - - - - - - rs909538 1:23854873 G - ENSR00001038646 RegulatoryFeature regulatory_region_variant - - - - - - rs909538 1:23854873 G ENSESTG00000034981 ENSESTT00000088413 Transcript intron_variant - - - - - - rs909538 1:23854873 G ENSESTG00000034979 ENSESTT00000088399 Transcript downstream_gene_variant - - - - - - DISTANCE=608 rs909538 1:23854873 G ENSESTG00000034981 ENSESTT00000088410 Transcript intron_variant - - - - - - rs909538 1:23854873 G CCDS236.1 CCDS236.1 Transcript intron_variant - - - - - - rs909538 1:23854873 G ENSESTG00000034981 ENSESTT00000088406 Transcript intron_variant - - - - - - rs909538 1:23854873 G 1870 NM_004091.3 Transcript intron_variant - - - - - - rs2813877 1:23923938 C - ENSR00000280273 RegulatoryFeature regulatory_region_variant - - - - - - rs2813877 1:23923938 C - - - intergenic_variant - - - - - - rs10737475 1:24006061 G - - - intergenic_variant - - - - - - rs195715 1:24823808 T 100750325 NR_045408.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs195715 1:24823808 T 100750325 NR_045407.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs195715 1:24823808 T 100750325 NR_045409.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4486394 1:24959560 C ENSESTG00000016061 ENSESTT00000040260 Transcript 5_prime_UTR_variant 88 - - - - - rs10732911 1:25122341 G ENSESTG00000016228 ENSESTT00000040851 Transcript intron_variant - - - - - - rs10732911 1:25122341 G ENSESTG00000016228 ENSESTT00000040827 Transcript intron_variant - - - - - - rs10732911 1:25122341 G CCDS256.1 CCDS256.1 Transcript intron_variant - - - - - - rs10732911 1:25122341 G 25932 NM_013943.2 Transcript intron_variant - - - - - - rs7517623 1:25132202 C - ENSR00000532830 RegulatoryFeature regulatory_region_variant - - - - - - rs7517623 1:25132202 C ENSESTG00000016228 ENSESTT00000040851 Transcript intron_variant - - - - - - rs7517623 1:25132202 C ENSESTG00000016228 ENSESTT00000040827 Transcript intron_variant - - - - - - rs7517623 1:25132202 C CCDS256.1 CCDS256.1 Transcript intron_variant - - - - - - rs7517623 1:25132202 C 25932 NM_013943.2 Transcript intron_variant - - - - - - rs4649029 1:25178969 G - - - intergenic_variant - - - - - - rs4456051 1:25185709 G - - - intergenic_variant - - - - - - rs6600241 1:25214954 C - - - intergenic_variant - - - - - - rs4141976 1:25380586 C - - - intergenic_variant - - - - - - rs61776815 1:25860718 C ENSESTG00000016675 ENSESTT00000041800 Transcript intron_variant - - - - - - rs1267219 1:26025916 G ENSESTG00000024449 ENSESTT00000062036 Transcript intron_variant - - - - - - rs1267219 1:26025916 G ENSESTG00000024449 ENSESTT00000062051 Transcript intron_variant - - - - - - rs1267219 1:26025916 G 57134 NM_020379.2 Transcript intron_variant - - - - - - rs1267219 1:26025916 G CCDS265.1 CCDS265.1 Transcript intron_variant - - - - - - rs2494400 1:26823872 G - - - intergenic_variant - - - - - - rs910048 1:27215784 T 54707 NM_018066.3 Transcript intron_variant - - - - - - rs910048 1:27215784 T CCDS289.1 CCDS289.1 Transcript intron_variant - - - - - - rs910048 1:27215784 T CCDS290.1 CCDS290.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1717 rs910048 1:27215784 T ENSESTG00000001239 ENSESTT00000002948 Transcript intron_variant - - - - - - rs910048 1:27215784 T ENSESTG00000001223 ENSESTT00000002922 Transcript downstream_gene_variant - - - - - - DISTANCE=1231 rs910048 1:27215784 T 63906 NM_022078.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1195 rs61783834 1:28754452 T ENSESTG00000003812 ENSESTT00000009679 Transcript intron_variant - - - - - - rs61783834 1:28754452 T ENSESTG00000003812 ENSESTT00000009676 Transcript intron_variant - - - - - - rs61783834 1:28754452 T CCDS41293.1 CCDS41293.1 Transcript intron_variant - - - - - - rs61783834 1:28754452 T ENSESTG00000003812 ENSESTT00000009671 Transcript intron_variant - - - - - - rs61783834 1:28754452 T 65979 NM_001048183.1 Transcript intron_variant - - - - - - rs3001312 1:28915130 C ENSESTG00000002481 ENSESTT00000006143 Transcript upstream_gene_variant - - - - - - DISTANCE=3645 rs3001312 1:28915130 C ENSESTG00000002481 ENSESTT00000006149 Transcript upstream_gene_variant - - - - - - DISTANCE=3905 rs3001312 1:28915130 C 115273 NM_152304.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3582 rs3001312 1:28915130 C 115273 NM_001193532.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3877 rs7530640 1:30268693 T - - - intergenic_variant - - - - - - rs166520 1:30437960 G - - - intergenic_variant - - - - - - rs788607 1:30862160 A - - - intergenic_variant - - - - - - rs262580 1:30958889 T - - - intergenic_variant - - - - - - rs12027737 1:31312903 G - - - intergenic_variant - - - - - - rs4949346 1:31593436 G - ENSR00000533828 RegulatoryFeature regulatory_region_variant - - - - - - rs4949346 1:31593436 G - - - intergenic_variant - - - - - - rs6425728 1:31744759 G ENSESTG00000005755 ENSESTT00000014614 Transcript intron_variant - - - - - - rs6425728 1:31744759 G CCDS340.1 CCDS340.1 Transcript intron_variant - - - - - - rs6425728 1:31744759 G 9410 NM_004814.2 Transcript intron_variant - - - - - - rs6694279 1:31867719 C - ENSR00000533861 RegulatoryFeature regulatory_region_variant - - - - - - rs6694279 1:31867719 C ENSESTG00000005737 ENSESTT00000014522 Transcript downstream_gene_variant - - - - - - DISTANCE=1555 rs496510 1:32870840 A - ENSR00001518957 RegulatoryFeature regulatory_region_variant - - - - - - rs496510 1:32870840 A - - - intergenic_variant - - - - - - rs2019117 1:32940870 G ENSESTG00000001184 ENSESTT00000002816 Transcript downstream_gene_variant - - - - - - DISTANCE=4154 rs2019117 1:32940870 G CCDS44104.1 CCDS44104.1 Transcript intron_variant - - - - - - rs2019117 1:32940870 G 728116 NM_001145720.1 Transcript intron_variant - - - - - - rs704886 1:33065947 C 653121 NM_001040441.1 Transcript missense_variant 1738 1253 418 G/A gGt/gCt - PolyPhen=benign;SIFT=tolerated rs704886 1:33065947 C CCDS30664.1 CCDS30664.1 Transcript missense_variant 1253 1253 418 G/A gGt/gCt - PolyPhen=benign;SIFT=tolerated rs704886 1:33065947 C ENSESTG00000001243 ENSESTT00000002939 Transcript downstream_gene_variant - - - - - - DISTANCE=182 rs359959 1:33082642 C ENSESTG00000001980 ENSESTT00000004997 Transcript downstream_gene_variant - - - - - - DISTANCE=4794 rs359959 1:33082642 C 339487 NM_178547.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4663 rs359959 1:33082642 C ENSESTG00000001980 ENSESTT00000005012 Transcript downstream_gene_variant - - - - - - DISTANCE=4790 rs359959 1:33082642 C CCDS365.1 CCDS365.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4821 rs359959 1:33082642 C ENSESTG00000001980 ENSESTT00000004985 Transcript downstream_gene_variant - - - - - - DISTANCE=4832 rs359959 1:33082642 C ENSESTG00000001980 ENSESTT00000005026 Transcript downstream_gene_variant - - - - - - DISTANCE=4794 rs360493 1:33224270 C CCDS41298.1 CCDS41298.1 Transcript intron_variant - - - - - - rs360493 1:33224270 C 57648 NM_020888.2 Transcript intron_variant - - - - - - rs360493 1:33224270 C ENSESTG00000001413 ENSESTT00000003335 Transcript intron_variant - - - - - - rs360493 1:33224270 C ENSESTG00000001413 ENSESTT00000003329 Transcript intron_variant - - - - - - rs360493 1:33224270 C ENSESTG00000001413 ENSESTT00000003333 Transcript intron_variant - - - - - - rs702833 1:33314197 C ENSESTG00000001445 ENSESTT00000003442 Transcript intron_variant - - - - - - rs702833 1:33314197 C CCDS30666.1 CCDS30666.1 Transcript intron_variant - - - - - - rs702833 1:33314197 C ENSESTG00000001445 ENSESTT00000003464 Transcript intron_variant - - - - - - rs702833 1:33314197 C ENSESTG00000001445 ENSESTT00000003457 Transcript intron_variant - - - - - - rs702833 1:33314197 C 64766 NM_022753.3 Transcript intron_variant - - - - - - rs702833 1:33314197 C 64766 NM_001256121.1 Transcript intron_variant - - - - - - rs537409 1:34204503 G 114784 NM_052896.3 Transcript intron_variant - - - - - - rs537409 1:34204503 G CCDS380.1 CCDS380.1 Transcript intron_variant - - - - - - rs1321626 1:34326409 C ENSESTG00000019434 ENSESTT00000048816 Transcript upstream_gene_variant - - - - - - DISTANCE=1373 rs1321626 1:34326409 C 114784 NM_052896.3 Transcript intron_variant - - - - - - rs1321626 1:34326409 C 127540 NM_145205.4 Transcript 5_prime_UTR_variant 334 - - - - - rs1321626 1:34326409 C CCDS30668.1 CCDS30668.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3384 rs1321626 1:34326409 C ENSESTG00000019434 ENSESTT00000048804 Transcript synonymous_variant 334 102 34 S tcT/tcC - rs1321626 1:34326409 C CCDS380.1 CCDS380.1 Transcript intron_variant - - - - - - rs1321626 1:34326409 C 127540 NR_033264.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3271 rs483973 1:34412436 G 114784 NM_052896.3 Transcript intron_variant - - - - - - rs483973 1:34412436 G CCDS380.1 CCDS380.1 Transcript intron_variant - - - - - - rs798070 1:34939611 C - - - intergenic_variant - - - - - - rs1088462 1:34978611 A - - - intergenic_variant - - - - - - rs1764407 1:35195747 T - - - intergenic_variant - - - - - - rs2753269 1:35238163 T ENSESTG00000035070 ENSESTT00000088634 Transcript intron_variant - - - - - - rs2935950 1:35557223 C 79830 NM_024772.3 Transcript intron_variant - - - - - - rs2935950 1:35557223 C ENSESTG00000034969 ENSESTT00000088390 Transcript intron_variant - - - - - - rs2935950 1:35557223 C ENSESTG00000034969 ENSESTT00000088379 Transcript intron_variant - - - - - - rs2935950 1:35557223 C ENSESTG00000034969 ENSESTT00000088371 Transcript intron_variant - - - - - - rs2935950 1:35557223 C CCDS41302.1 CCDS41302.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2366 rs2935950 1:35557223 C ENSESTG00000034969 ENSESTT00000088381 Transcript intron_variant - - - - - - rs12061188 1:35557835 G 79830 NM_024772.3 Transcript intron_variant - - - - - - rs12061188 1:35557835 G ENSESTG00000034969 ENSESTT00000088390 Transcript intron_variant - - - - - - rs12061188 1:35557835 G ENSESTG00000034969 ENSESTT00000088379 Transcript intron_variant - - - - - - rs12061188 1:35557835 G ENSESTG00000034969 ENSESTT00000088371 Transcript intron_variant - - - - - - rs12061188 1:35557835 G CCDS41302.1 CCDS41302.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1754 rs12061188 1:35557835 G ENSESTG00000034969 ENSESTT00000088381 Transcript intron_variant - - - - - - rs507058 1:36674179 A - - - intergenic_variant - - - - - - rs2995226 1:36738941 T - ENSR00000281432 RegulatoryFeature regulatory_region_variant - - - - - - rs2995226 1:36738941 T ENSESTG00000001078 ENSESTT00000002604 Transcript intron_variant - - - - - - rs2995226 1:36738941 T ENSESTG00000001078 ENSESTT00000002607 Transcript intron_variant - - - - - - rs2995226 1:36738941 T 9967 NM_005119.3 Transcript intron_variant - - - - - - rs215767 1:37585102 G - - - intergenic_variant - - - - - - rs215786 1:37615622 A - - - intergenic_variant - - - - - - rs215753 1:37631581 T 100422898 NR_036217.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4346 rs2811623 1:37876225 T - - - intergenic_variant - - - - - - rs2811634 1:37884829 G - - - intergenic_variant - - - - - - rs4653290 1:37891948 T - - - intergenic_variant - - - - - - rs7412302 1:37900771 C - - - intergenic_variant - - - - - - rs2660559 1:37926973 G ENSESTG00000006678 ENSESTT00000016919 Transcript intron_variant - - - - - - rs2660559 1:37926973 G 728431 NR_038842.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2456803 1:37940657 A - ENSR00000669678 RegulatoryFeature regulatory_region_variant - - - - - - rs2456803 1:37940657 A ENSESTG00000006362 ENSESTT00000016050 Transcript upstream_gene_variant - - - - - - DISTANCE=2383 rs2456803 1:37940657 A ENSESTG00000006355 ENSESTT00000016038 Transcript intron_variant - - - - - - rs2456803 1:37940657 A ENSESTG00000006355 ENSESTT00000016044 Transcript intron_variant - - - - - - rs2456803 1:37940657 A ENSESTG00000006678 ENSESTT00000016919 Transcript upstream_gene_variant - - - - - - DISTANCE=681 rs2456803 1:37940657 A 728431 NR_038842.1 Transcript upstream_gene_variant - - - - - - DISTANCE=613 rs2456803 1:37940657 A ENSESTG00000006362 ENSESTT00000016065 Transcript upstream_gene_variant - - - - - - DISTANCE=4940 rs2456803 1:37940657 A CCDS417.1 CCDS417.1 Transcript upstream_gene_variant - - - - - - DISTANCE=441 rs2456803 1:37940657 A 80149 NM_025079.2 Transcript intron_variant - - - - - - rs215196 1:38007874 G ENSESTG00000006639 ENSESTT00000016822 Transcript intron_variant - - - - - - rs215196 1:38007874 G 79753 NM_024700.3 Transcript intron_variant - - - - - - rs215196 1:38007874 G CCDS419.1 CCDS419.1 Transcript intron_variant - - - - - - rs4311850 1:38098854 G CCDS55591.1 CCDS55591.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3281 rs4311850 1:38098854 G 284654 NM_001242909.1 Transcript intron_variant - - - - - - rs4311850 1:38098854 G 284654 NM_001242908.1 Transcript intron_variant - - - - - - rs4311850 1:38098854 G CCDS41304.1 CCDS41304.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3521 rs4311850 1:38098854 G CCDS55590.1 CCDS55590.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3521 rs4311850 1:38098854 G 284654 NM_001242910.1 Transcript intron_variant - - - - - - rs4311850 1:38098854 G 284654 NM_001038633.3 Transcript intron_variant - - - - - - rs4311850 1:38098854 G ENSESTG00000006610 ENSESTT00000016673 Transcript intron_variant - - - - - - rs4653313 1:38115044 C - - - intergenic_variant - - - - - - rs4652972 1:38400013 T ENSESTG00000006540 ENSESTT00000016535 Transcript intron_variant - - - - - - rs4652972 1:38400013 T ENSESTG00000006540 ENSESTT00000016539 Transcript upstream_gene_variant - - - - - - DISTANCE=2550 rs4652972 1:38400013 T CCDS41306.1 CCDS41306.1 Transcript intron_variant - - - - - - rs4652972 1:38400013 T ENSESTG00000006540 ENSESTT00000016529 Transcript intron_variant - - - - - - rs4652972 1:38400013 T 3633 NM_005540.2 Transcript intron_variant - - - - - - rs4652972 1:38400013 T ENSESTG00000006540 ENSESTT00000016558 Transcript upstream_gene_variant - - - - - - DISTANCE=2550 rs4308945 1:38658803 T - - - intergenic_variant - - - - - - rs2798794 1:38809618 T - - - intergenic_variant - - - - - - rs2985767 1:39070392 A - ENSR00000534794 RegulatoryFeature regulatory_region_variant - - - - - - rs2985767 1:39070392 A - - - intergenic_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072641 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072662 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072623 Transcript downstream_gene_variant - - - - - - DISTANCE=4178 rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072687 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000071896 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072678 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072607 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072552 Transcript intron_variant - - - - - - rs645234 1:39899177 T CCDS435.1 CCDS435.1 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072560 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000071868 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072671 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072586 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072720 Transcript intron_variant - - - - - - rs645234 1:39899177 T 23499 NM_012090.4 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072643 Transcript intron_variant - - - - - - rs645234 1:39899177 T ENSESTG00000028507 ENSESTT00000072577 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072641 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072762 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072662 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072776 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072687 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000071896 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072678 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072812 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072552 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072788 Transcript intron_variant - - - - - - rs1623310 1:39939199 G CCDS435.1 CCDS435.1 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072560 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000071868 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072671 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072586 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072735 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072786 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072825 Transcript intron_variant - - - - - - rs1623310 1:39939199 G 23499 NM_012090.4 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072643 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072577 Transcript intron_variant - - - - - - rs1623310 1:39939199 G ENSESTG00000028507 ENSESTT00000072747 Transcript intron_variant - - - - - - rs704770 1:40160570 A 51440 NM_016257.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3481 rs704770 1:40160570 A ENSESTG00000029883 ENSESTT00000075213 Transcript upstream_gene_variant - - - - - - DISTANCE=3466 rs209615 1:40896262 G - - - intergenic_variant - - - - - - rs7523852 1:40975104 T ENSESTG00000026182 ENSESTT00000066069 Transcript intron_variant - - - - - - rs7523852 1:40975104 T ENSESTG00000026182 ENSESTT00000066048 Transcript intron_variant - - - - - - rs7523852 1:40975104 T 64789 NM_022774.1 Transcript intron_variant - - - - - - rs7523852 1:40975104 T ENSESTG00000026182 ENSESTT00000066024 Transcript intron_variant - - - - - - rs6676897 1:41168817 C - ENSR00000535125 RegulatoryFeature regulatory_region_variant - - - - - - rs6676897 1:41168817 C 4802 NM_001142587.1 Transcript intron_variant - - - - - - rs6676897 1:41168817 C 4802 NM_001142589.1 Transcript intron_variant - - - - - - rs6676897 1:41168817 C ENSESTG00000026265 ENSESTT00000066410 Transcript intron_variant - - - - - - rs6676897 1:41168817 C ENSESTG00000026265 ENSESTT00000066193 Transcript intron_variant - - - - - - rs6676897 1:41168817 C ENSESTG00000026265 ENSESTT00000066380 Transcript intron_variant - - - - - - rs6676897 1:41168817 C ENSESTG00000026265 ENSESTT00000066400 Transcript intron_variant - - - - - - rs6676897 1:41168817 C 4802 NM_001142588.1 Transcript intron_variant - - - - - - rs6676897 1:41168817 C ENSESTG00000026265 ENSESTT00000066384 Transcript intron_variant - - - - - - rs6676897 1:41168817 C 4802 NM_014223.4 Transcript intron_variant - - - - - - rs6676897 1:41168817 C 4802 NM_001142590.1 Transcript intron_variant - - - - - - rs2744795 1:41170397 G 4802 NM_001142587.1 Transcript intron_variant - - - - - - rs2744795 1:41170397 G 4802 NM_001142589.1 Transcript intron_variant - - - - - - rs2744795 1:41170397 G ENSESTG00000026265 ENSESTT00000066410 Transcript intron_variant - - - - - - rs2744795 1:41170397 G ENSESTG00000026265 ENSESTT00000066193 Transcript intron_variant - - - - - - rs2744795 1:41170397 G ENSESTG00000026265 ENSESTT00000066380 Transcript intron_variant - - - - - - rs2744795 1:41170397 G ENSESTG00000026265 ENSESTT00000066400 Transcript intron_variant - - - - - - rs2744795 1:41170397 G 4802 NM_001142588.1 Transcript intron_variant - - - - - - rs2744795 1:41170397 G ENSESTG00000026265 ENSESTT00000066384 Transcript intron_variant - - - - - - rs2744795 1:41170397 G 4802 NM_014223.4 Transcript intron_variant - - - - - - rs2744795 1:41170397 G ENSESTG00000026265 ENSESTT00000066452 Transcript upstream_gene_variant - - - - - - DISTANCE=4598 rs2744795 1:41170397 G 4802 NM_001142590.1 Transcript intron_variant - - - - - - rs823688 1:41263942 G 9132 NM_172163.2 Transcript intron_variant - - - - - - rs823688 1:41263942 G CCDS456.1 CCDS456.1 Transcript intron_variant - - - - - - rs823688 1:41263942 G 9132 NM_004700.3 Transcript intron_variant - - - - - - rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000066891 Transcript upstream_gene_variant - - - - - - DISTANCE=1027 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000066898 Transcript upstream_gene_variant - - - - - - DISTANCE=1027 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000067030 Transcript upstream_gene_variant - - - - - - DISTANCE=3732 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000066946 Transcript upstream_gene_variant - - - - - - DISTANCE=1800 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000066882 Transcript upstream_gene_variant - - - - - - DISTANCE=1027 rs1892553 1:41443980 A CCDS459.1 CCDS459.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4983 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000067037 Transcript upstream_gene_variant - - - - - - DISTANCE=3732 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000066929 Transcript upstream_gene_variant - - - - - - DISTANCE=1413 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000066923 Transcript upstream_gene_variant - - - - - - DISTANCE=1413 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000066989 Transcript upstream_gene_variant - - - - - - DISTANCE=3550 rs1892553 1:41443980 A 1503 NM_001905.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1027 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000067051 Transcript upstream_gene_variant - - - - - - DISTANCE=3732 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000067008 Transcript upstream_gene_variant - - - - - - DISTANCE=3550 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000066910 Transcript upstream_gene_variant - - - - - - DISTANCE=1413 rs1892553 1:41443980 A ENSESTG00000026458 ENSESTT00000067016 Transcript upstream_gene_variant - - - - - - DISTANCE=3550 rs7541316 1:41737898 G ENSESTG00000026664 ENSESTT00000067152 Transcript intron_variant - - - - - - rs10749840 1:42105564 C - ENSR00001519570 RegulatoryFeature regulatory_region_variant - - - - - - rs10749840 1:42105564 C 59269 NM_024503.4 Transcript intron_variant - - - - - - rs10749840 1:42105564 C 59269 NM_001127714.2 Transcript intron_variant - - - - - - rs591560 1:42438311 T ENSESTG00000014624 ENSESTT00000036582 Transcript intron_variant - - - - - - rs591560 1:42438311 T 59269 NR_038261.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7512105 1:42568080 G - - - intergenic_variant - - - - - - rs11210586 1:42575675 A - - - intergenic_variant - - - - - - rs4660662 1:43212431 G CCDS53307.1 CCDS53307.1 Transcript downstream_gene_variant - - - - - - DISTANCE=73 rs4660662 1:43212431 G 64175 NM_001146289.1 Transcript 3_prime_UTR_variant 2280 - - - - - rs4660662 1:43212431 G CCDS472.2 CCDS472.2 Transcript synonymous_variant 2148 2148 716 G ggT/ggC - rs4660662 1:43212431 G 64175 NM_001243246.1 Transcript 3_prime_UTR_variant 2680 - - - - - rs4660662 1:43212431 G CCDS57986.1 CCDS57986.1 Transcript downstream_gene_variant - - - - - - DISTANCE=152 rs4660662 1:43212431 G ENSESTG00000001989 ENSESTT00000005021 Transcript intron_variant - - - - - - rs4660662 1:43212431 G 64175 NM_022356.3 Transcript synonymous_variant 2261 2148 716 G ggT/ggC - rs4660662 1:43212431 G ENSESTG00000001989 ENSESTT00000005033 Transcript intron_variant - - - - - - rs4660662 1:43212431 G ENSESTG00000001989 ENSESTT00000005061 Transcript downstream_gene_variant - - - - - - DISTANCE=70 rs1199138 1:43791511 T ENSESTG00000001828 ENSESTT00000004563 Transcript downstream_gene_variant - - - - - - DISTANCE=2733 rs1199138 1:43791511 T 7075 NM_001253357.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2730 rs1199138 1:43791511 T CCDS482.1 CCDS482.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3118 rs1199138 1:43791511 T ENSESTG00000001828 ENSESTT00000004601 Transcript downstream_gene_variant - - - - - - DISTANCE=2733 rs1199138 1:43791511 T ENSESTG00000001828 ENSESTT00000004617 Transcript downstream_gene_variant - - - - - - DISTANCE=2733 rs1199138 1:43791511 T 7075 NM_005424.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2730 rs1199138 1:43791511 T ENSESTG00000001828 ENSESTT00000004592 Transcript downstream_gene_variant - - - - - - DISTANCE=2733 rs803373 1:44653775 A - - - intergenic_variant - - - - - - rs609355 1:44784993 G 79033 NM_024066.1 Transcript intron_variant - - - - - - rs609355 1:44784993 G ENSESTG00000004585 ENSESTT00000011579 Transcript intron_variant - - - - - - rs609355 1:44784993 G ENSESTG00000004585 ENSESTT00000011576 Transcript intron_variant - - - - - - rs609355 1:44784993 G ENSESTG00000004585 ENSESTT00000011571 Transcript intron_variant - - - - - - rs609355 1:44784993 G CCDS30696.1 CCDS30696.1 Transcript intron_variant - - - - - - rs609355 1:44784993 G ENSESTG00000004585 ENSESTT00000011586 Transcript intron_variant - - - - - - rs226061 1:44801260 C 79033 NM_024066.1 Transcript intron_variant - - - - - - rs226061 1:44801260 C ENSESTG00000004585 ENSESTT00000011579 Transcript intron_variant - - - - - - rs226061 1:44801260 C ENSESTG00000004585 ENSESTT00000011576 Transcript intron_variant - - - - - - rs226061 1:44801260 C ENSESTG00000004585 ENSESTT00000011571 Transcript intron_variant - - - - - - rs226061 1:44801260 C CCDS30696.1 CCDS30696.1 Transcript intron_variant - - - - - - rs226061 1:44801260 C ENSESTG00000004585 ENSESTT00000011586 Transcript intron_variant - - - - - - rs170479 1:44864251 A - - - intergenic_variant - - - - - - rs1538885 1:44906142 C CCDS510.1 CCDS510.1 Transcript intron_variant - - - - - - rs1538885 1:44906142 C ENSESTG00000017969 ENSESTT00000045320 Transcript intron_variant - - - - - - rs1538885 1:44906142 C ENSESTG00000017969 ENSESTT00000045304 Transcript intron_variant - - - - - - rs1538885 1:44906142 C ENSESTG00000017969 ENSESTT00000045286 Transcript intron_variant - - - - - - rs1538885 1:44906142 C ENSESTG00000017969 ENSESTT00000045278 Transcript intron_variant - - - - - - rs1538885 1:44906142 C 55182 NM_018150.2 Transcript intron_variant - - - - - - rs7545709 1:44943378 A CCDS510.1 CCDS510.1 Transcript intron_variant - - - - - - rs7545709 1:44943378 A ENSESTG00000017969 ENSESTT00000045320 Transcript intron_variant - - - - - - rs7545709 1:44943378 A ENSESTG00000017969 ENSESTT00000045304 Transcript intron_variant - - - - - - rs7545709 1:44943378 A ENSESTG00000017969 ENSESTT00000045286 Transcript intron_variant - - - - - - rs7545709 1:44943378 A ENSESTG00000017969 ENSESTT00000045278 Transcript intron_variant - - - - - - rs7545709 1:44943378 A 55182 NM_018150.2 Transcript intron_variant - - - - - - rs7552668 1:44946060 C CCDS510.1 CCDS510.1 Transcript intron_variant - - - - - - rs7552668 1:44946060 C ENSESTG00000017969 ENSESTT00000045320 Transcript intron_variant - - - - - - rs7552668 1:44946060 C ENSESTG00000017969 ENSESTT00000045304 Transcript intron_variant - - - - - - rs7552668 1:44946060 C ENSESTG00000017969 ENSESTT00000045286 Transcript intron_variant - - - - - - rs7552668 1:44946060 C ENSESTG00000017969 ENSESTT00000045278 Transcript intron_variant - - - - - - rs7552668 1:44946060 C 55182 NM_018150.2 Transcript intron_variant - - - - - - rs3008977 1:45193622 A ENSESTG00000018120 ENSESTT00000045638 Transcript downstream_gene_variant - - - - - - DISTANCE=3570 rs3008977 1:45193622 A 339541 NM_001145636.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2359 rs3008977 1:45193622 A ENSESTG00000018120 ENSESTT00000045659 Transcript downstream_gene_variant - - - - - - DISTANCE=3570 rs3008977 1:45193622 A ENSESTG00000018120 ENSESTT00000045671 Transcript downstream_gene_variant - - - - - - DISTANCE=3748 rs3008977 1:45193622 A CCDS53311.1 CCDS53311.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2547 rs3008977 1:45193622 A ENSESTG00000018120 ENSESTT00000045677 Transcript downstream_gene_variant - - - - - - DISTANCE=3570 rs3008977 1:45193622 A 26830 NR_002755.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3119 rs3008977 1:45193622 A ENSESTG00000018120 ENSESTT00000045688 Transcript downstream_gene_variant - - - - - - DISTANCE=3607 rs6674839 1:45471054 G 79654 NM_024602.5 Transcript intron_variant - - - - - - rs6674839 1:45471054 G CCDS41318.1 CCDS41318.1 Transcript intron_variant - - - - - - rs6429552 1:45475566 G ENSESTG00000018433 ENSESTT00000046460 Transcript upstream_gene_variant - - - - - - DISTANCE=3708 rs6429552 1:45475566 G 7389 NR_036510.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2239 rs6429552 1:45475566 G 7389 NM_000374.4 Transcript upstream_gene_variant - - - - - - DISTANCE=2239 rs6429552 1:45475566 G ENSESTG00000018402 ENSESTT00000046358 Transcript upstream_gene_variant - - - - - - DISTANCE=2317 rs6429552 1:45475566 G 79654 NM_024602.5 Transcript intron_variant - - - - - - rs6429552 1:45475566 G CCDS41318.1 CCDS41318.1 Transcript intron_variant - - - - - - rs6429552 1:45475566 G CCDS518.1 CCDS518.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2372 rs1814166 1:45519186 C CCDS41319.1 CCDS41319.1 Transcript intron_variant - - - - - - rs1814166 1:45519186 C 57643 NM_020883.1 Transcript intron_variant - - - - - - rs781233 1:45894226 G ENSESTG00000025509 ENSESTT00000064394 Transcript intron_variant - - - - - - rs781233 1:45894226 G ENSESTG00000025509 ENSESTT00000064381 Transcript intron_variant - - - - - - rs781233 1:45894226 G 10420 NM_007170.2 Transcript intron_variant - - - - - - rs781233 1:45894226 G CCDS41323.1 CCDS41323.1 Transcript intron_variant - - - - - - rs781233 1:45894226 G ENSESTG00000025509 ENSESTT00000064371 Transcript intron_variant - - - - - - rs781233 1:45894226 G ENSESTG00000025509 ENSESTT00000064405 Transcript intron_variant - - - - - - rs781233 1:45894226 G ENSESTG00000018501 ENSESTT00000046624 Transcript intron_variant - - - - - - rs781233 1:45894226 G ENSESTG00000018501 ENSESTT00000046654 Transcript intron_variant - - - - - - rs3014231 1:46145528 C ENSESTG00000025098 ENSESTT00000063520 Transcript intron_variant - - - - - - rs3014231 1:46145528 C 60313 NM_021639.4 Transcript intron_variant - - - - - - rs3014231 1:46145528 C ENSESTG00000023288 ENSESTT00000058784 Transcript intron_variant - - - - - - rs3014231 1:46145528 C ENSESTG00000025098 ENSESTT00000063529 Transcript intron_variant - - - - - - rs3014231 1:46145528 C ENSESTG00000025098 ENSESTT00000063565 Transcript intron_variant - - - - - - rs3014231 1:46145528 C ENSESTG00000025098 ENSESTT00000063321 Transcript intron_variant - - - - - - rs7519859 1:46263283 A ENSESTG00000023371 ENSESTT00000058951 Transcript intron_variant - - - - - - rs4417003 1:46367394 G 23139 NM_015112.2 Transcript intron_variant - - - - - - rs4417003 1:46367394 G ENSESTG00000023371 ENSESTT00000058951 Transcript intron_variant - - - - - - rs4417003 1:46367394 G ENSESTG00000023371 ENSESTT00000059300 Transcript intron_variant - - - - - - rs4417003 1:46367394 G CCDS41326.1 CCDS41326.1 Transcript intron_variant - - - - - - rs4417003 1:46367394 G ENSESTG00000023371 ENSESTT00000059316 Transcript intron_variant - - - - - - rs4417003 1:46367394 G ENSESTG00000023371 ENSESTT00000059281 Transcript intron_variant - - - - - - rs4417003 1:46367394 G ENSESTG00000023371 ENSESTT00000058968 Transcript intron_variant - - - - - - rs4660897 1:46390204 C ENSESTG00000023371 ENSESTT00000059300 Transcript intron_variant - - - - - - rs4660897 1:46390204 C ENSESTG00000023371 ENSESTT00000059370 Transcript intron_variant - - - - - - rs4660897 1:46390204 C ENSESTG00000023371 ENSESTT00000058951 Transcript intron_variant - - - - - - rs4660897 1:46390204 C 23139 NM_015112.2 Transcript intron_variant - - - - - - rs4660897 1:46390204 C CCDS41326.1 CCDS41326.1 Transcript intron_variant - - - - - - rs4660897 1:46390204 C ENSESTG00000023371 ENSESTT00000059316 Transcript intron_variant - - - - - - rs4660897 1:46390204 C ENSESTG00000023371 ENSESTT00000059281 Transcript intron_variant - - - - - - rs4660897 1:46390204 C ENSESTG00000023371 ENSESTT00000058968 Transcript intron_variant - - - - - - rs4660897 1:46390204 C ENSESTG00000023371 ENSESTT00000059361 Transcript intron_variant - - - - - - rs1258029 1:47009099 G CCDS44133.1 CCDS44133.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4303 rs1258029 1:47009099 G 148930 NM_001097611.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2217 rs1258029 1:47009099 G 100507423 NR_038403.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1258020 1:47067580 T ENSESTG00000010065 ENSESTT00000025225 Transcript intron_variant - - - - - - rs1258020 1:47067580 T 8569 NM_198973.3 Transcript intron_variant - - - - - - rs1258020 1:47067580 T 8569 NR_024176.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs1258020 1:47067580 T 8569 NR_024174.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs1258020 1:47067580 T ENSESTG00000010065 ENSESTT00000025233 Transcript intron_variant - - - - - - rs1258020 1:47067580 T ENSESTG00000010065 ENSESTT00000025219 Transcript intron_variant - - - - - - rs1258020 1:47067580 T ENSESTG00000010065 ENSESTT00000025230 Transcript intron_variant - - - - - - rs1258020 1:47067580 T 8569 NM_003684.5 Transcript intron_variant - - - - - - rs1258020 1:47067580 T 8569 NM_001135553.2 Transcript intron_variant - - - - - - rs1258020 1:47067580 T ENSESTG00000010065 ENSESTT00000025213 Transcript intron_variant - - - - - - rs1258071 1:47098138 T 64756 NM_001256418.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2573 rs1258071 1:47098138 T ENSESTG00000010029 ENSESTT00000025119 Transcript downstream_gene_variant - - - - - - DISTANCE=3152 rs1258071 1:47098138 T 64756 NM_001243728.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2573 rs1258071 1:47098138 T 64756 NM_001042546.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2573 rs1258071 1:47098138 T CCDS57997.1 CCDS57997.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3310 rs1258071 1:47098138 T CCDS541.2 CCDS541.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3310 rs1258071 1:47098138 T CCDS57998.1 CCDS57998.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3310 rs1258071 1:47098138 T CCDS41327.2 CCDS41327.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3310 rs1258071 1:47098138 T 64756 NM_022745.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2573 rs1258071 1:47098138 T ENSESTG00000010029 ENSESTT00000025130 Transcript downstream_gene_variant - - - - - - DISTANCE=3152 rs942080 1:47102058 T 64756 NM_001256418.1 Transcript intron_variant - - - - - - rs942080 1:47102058 T ENSESTG00000010029 ENSESTT00000025119 Transcript intron_variant - - - - - - rs942080 1:47102058 T 64756 NM_001243728.1 Transcript intron_variant - - - - - - rs942080 1:47102058 T 64756 NM_001042546.2 Transcript intron_variant - - - - - - rs942080 1:47102058 T CCDS57997.1 CCDS57997.1 Transcript intron_variant - - - - - - rs942080 1:47102058 T CCDS541.2 CCDS541.2 Transcript intron_variant - - - - - - rs942080 1:47102058 T CCDS57998.1 CCDS57998.1 Transcript intron_variant - - - - - - rs942080 1:47102058 T CCDS41327.2 CCDS41327.2 Transcript intron_variant - - - - - - rs942080 1:47102058 T 64756 NM_022745.4 Transcript intron_variant - - - - - - rs942080 1:47102058 T ENSESTG00000010029 ENSESTT00000025130 Transcript intron_variant - - - - - - rs1258060 1:47105617 C 64756 NM_001256418.1 Transcript intron_variant - - - - - - rs1258060 1:47105617 C ENSESTG00000010029 ENSESTT00000025119 Transcript intron_variant - - - - - - rs1258060 1:47105617 C 64756 NM_001243728.1 Transcript intron_variant - - - - - - rs1258060 1:47105617 C 64756 NM_001042546.2 Transcript intron_variant - - - - - - rs1258060 1:47105617 C CCDS57997.1 CCDS57997.1 Transcript intron_variant - - - - - - rs1258060 1:47105617 C CCDS541.2 CCDS541.2 Transcript intron_variant - - - - - - rs1258060 1:47105617 C CCDS57998.1 CCDS57998.1 Transcript intron_variant - - - - - - rs1258060 1:47105617 C CCDS41327.2 CCDS41327.2 Transcript intron_variant - - - - - - rs1258060 1:47105617 C 64756 NM_022745.4 Transcript intron_variant - - - - - - rs1258060 1:47105617 C ENSESTG00000010029 ENSESTT00000025130 Transcript intron_variant - - - - - - rs638147 1:47231137 C - - - intergenic_variant - - - - - - rs596400 1:47256478 G - - - intergenic_variant - - - - - - rs7522266 1:47379776 C - - - intergenic_variant - - - - - - rs1502927 1:47548670 G 199974 NM_178134.2 Transcript intron_variant - - - - - - rs1502927 1:47548670 G CCDS545.1 CCDS545.1 Transcript intron_variant - - - - - - rs1502927 1:47548670 G ENSESTG00000009868 ENSESTT00000024708 Transcript intron_variant - - - - - - rs2821076 1:47648373 T - ENSR00000282264 RegulatoryFeature regulatory_region_variant - - - - - - rs2821076 1:47648373 T CCDS546.1 CCDS546.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1270 rs2821076 1:47648373 T 100874253 NR_047498.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2362 rs2821076 1:47648373 T 10158 NM_005764.3 Transcript downstream_gene_variant - - - - - - DISTANCE=888 rs927462 1:47685455 C 6886 NM_003189.2 Transcript synonymous_variant 1510 933 311 K aaA/aaG - rs927462 1:47685455 C CCDS547.1 CCDS547.1 Transcript synonymous_variant 933 933 311 K aaA/aaG - rs2820979 1:47856590 C - ENSR00000536119 RegulatoryFeature regulatory_region_variant - - - - - - rs2820979 1:47856590 C ENSESTG00000009942 ENSESTT00000024854 Transcript intron_variant - - - - - - rs6588390 1:47900463 T - ENSR00000536124 RegulatoryFeature regulatory_region_variant - - - - - - rs6588390 1:47900463 T CCDS30708.1 CCDS30708.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3345 rs6588390 1:47900463 T ENSESTG00000025358 ENSESTT00000063950 Transcript downstream_gene_variant - - - - - - DISTANCE=1896 rs6588390 1:47900463 T ENSESTG00000025656 ENSESTT00000064703 Transcript intron_variant - - - - - - rs6588390 1:47900463 T 2306 NM_004474.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1226 rs6588390 1:47900463 T 84793 NR_026878.1 Transcript upstream_gene_variant - - - - - - DISTANCE=150 rs2506974 1:48031389 C - - - intergenic_variant - - - - - - rs2506973 1:48035083 A - - - intergenic_variant - - - - - - rs2506972 1:48036366 G - - - intergenic_variant - - - - - - rs2457065 1:48036930 C - - - intergenic_variant - - - - - - rs2457064 1:48039063 G - - - intergenic_variant - - - - - - rs1249087 1:48109516 T - - - intergenic_variant - - - - - - rs893759 1:48181535 C - - - intergenic_variant - - - - - - rs6670752 1:48290576 C ENSESTG00000025590 ENSESTT00000064608 Transcript intron_variant - - - - - - rs6670752 1:48290576 C CCDS58000.1 CCDS58000.1 Transcript intron_variant - - - - - - rs6670752 1:48290576 C ENSESTG00000025638 ENSESTT00000064668 Transcript upstream_gene_variant - - - - - - DISTANCE=3031 rs6670752 1:48290576 C 388630 NM_001194986.1 Transcript intron_variant - - - - - - rs6670752 1:48290576 C ENSESTG00000025590 ENSESTT00000064579 Transcript intron_variant - - - - - - rs1890319 1:48856382 A ENSESTG00000025453 ENSESTT00000064324 Transcript intron_variant - - - - - - rs1890319 1:48856382 A ENSESTG00000025453 ENSESTT00000064282 Transcript intron_variant - - - - - - rs1890319 1:48856382 A ENSESTG00000025453 ENSESTT00000064358 Transcript intron_variant - - - - - - rs1890319 1:48856382 A ENSESTG00000025453 ENSESTT00000064272 Transcript intron_variant - - - - - - rs1890319 1:48856382 A ENSESTG00000025453 ENSESTT00000064346 Transcript intron_variant - - - - - - rs1890319 1:48856382 A 54558 NM_019073.2 Transcript intron_variant - - - - - - rs1890319 1:48856382 A ENSESTG00000025453 ENSESTT00000064254 Transcript intron_variant - - - - - - rs1890319 1:48856382 A ENSESTG00000025453 ENSESTT00000064326 Transcript intron_variant - - - - - - rs1890319 1:48856382 A CCDS551.1 CCDS551.1 Transcript intron_variant - - - - - - rs1832760 1:49521784 C 84871 NM_032785.3 Transcript intron_variant - - - - - - rs1832760 1:49521784 C CCDS44137.1 CCDS44137.1 Transcript intron_variant - - - - - - rs1338217 1:49855947 T 84871 NM_032785.3 Transcript intron_variant - - - - - - rs1338217 1:49855947 T CCDS44137.1 CCDS44137.1 Transcript intron_variant - - - - - - rs6694973 1:50136989 A 84871 NM_032785.3 Transcript intron_variant - - - - - - rs6694973 1:50136989 A CCDS44137.1 CCDS44137.1 Transcript intron_variant - - - - - - rs6694973 1:50136989 A ENSESTG00000003451 ENSESTT00000008636 Transcript intron_variant - - - - - - rs6694973 1:50136989 A ENSESTG00000003451 ENSESTT00000008616 Transcript intron_variant - - - - - - rs4615885 1:50256294 A 84871 NM_032785.3 Transcript intron_variant - - - - - - rs4615885 1:50256294 A CCDS44137.1 CCDS44137.1 Transcript intron_variant - - - - - - rs4615885 1:50256294 A ENSESTG00000003451 ENSESTT00000008636 Transcript intron_variant - - - - - - rs4615885 1:50256294 A ENSESTG00000003451 ENSESTT00000008633 Transcript intron_variant - - - - - - rs4615885 1:50256294 A ENSESTG00000003451 ENSESTT00000008616 Transcript intron_variant - - - - - - rs7533801 1:50310802 C 84871 NM_032785.3 Transcript intron_variant - - - - - - rs7533801 1:50310802 C CCDS44137.1 CCDS44137.1 Transcript intron_variant - - - - - - rs7533801 1:50310802 C ENSESTG00000003451 ENSESTT00000008636 Transcript intron_variant - - - - - - rs7533801 1:50310802 C ENSESTG00000003451 ENSESTT00000008633 Transcript intron_variant - - - - - - rs7533801 1:50310802 C ENSESTG00000003451 ENSESTT00000008616 Transcript intron_variant - - - - - - rs1278513 1:50904697 C - ENSR00000669964 RegulatoryFeature regulatory_region_variant - - - - - - rs1278513 1:50904697 C ENSESTG00000026964 ENSESTT00000068355 Transcript downstream_gene_variant - - - - - - DISTANCE=2250 rs1278513 1:50904697 C ENSESTG00000026964 ENSESTT00000068307 Transcript downstream_gene_variant - - - - - - DISTANCE=2250 rs1278513 1:50904697 C CCDS554.1 CCDS554.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2415 rs1278513 1:50904697 C ENSESTG00000026964 ENSESTT00000068341 Transcript downstream_gene_variant - - - - - - DISTANCE=2250 rs1278513 1:50904697 C ENSESTG00000003403 ENSESTT00000008499 Transcript intron_variant - - - - - - rs1278513 1:50904697 C ENSESTG00000026964 ENSESTT00000068325 Transcript downstream_gene_variant - - - - - - DISTANCE=2250 rs1278513 1:50904697 C 11124 NM_007051.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2238 rs1149796 1:50979643 T ENSESTG00000026964 ENSESTT00000068355 Transcript intron_variant - - - - - - rs1149796 1:50979643 T ENSESTG00000026964 ENSESTT00000068307 Transcript intron_variant - - - - - - rs1149796 1:50979643 T CCDS554.1 CCDS554.1 Transcript intron_variant - - - - - - rs1149796 1:50979643 T ENSESTG00000026964 ENSESTT00000068341 Transcript intron_variant - - - - - - rs1149796 1:50979643 T ENSESTG00000026964 ENSESTT00000068325 Transcript intron_variant - - - - - - rs1149796 1:50979643 T 11124 NM_007051.2 Transcript intron_variant - - - - - - rs4454589 1:51313583 C ENSESTG00000026964 ENSESTT00000068307 Transcript intron_variant - - - - - - rs4454589 1:51313583 C CCDS554.1 CCDS554.1 Transcript intron_variant - - - - - - rs4454589 1:51313583 C ENSESTG00000026964 ENSESTT00000067967 Transcript intron_variant - - - - - - rs4454589 1:51313583 C 11124 NM_007051.2 Transcript intron_variant - - - - - - rs2153765 1:51402835 G ENSESTG00000026964 ENSESTT00000067946 Transcript intron_variant - - - - - - rs2153765 1:51402835 G CCDS554.1 CCDS554.1 Transcript intron_variant - - - - - - rs2153765 1:51402835 G 11124 NM_007051.2 Transcript intron_variant - - - - - - rs2405246 1:52035232 A - ENSR00000536449 RegulatoryFeature regulatory_region_variant - - - - - - rs2405246 1:52035232 A - - - intergenic_variant - - - - - - rs7523255 1:52163425 T 114883 NM_148906.2 Transcript intron_variant - - - - - - rs7523255 1:52163425 T ENSESTG00000008957 ENSESTT00000022602 Transcript intron_variant - - - - - - rs7523255 1:52163425 T ENSESTG00000008957 ENSESTT00000022605 Transcript intron_variant - - - - - - rs7523255 1:52163425 T 114883 NM_148909.3 Transcript intron_variant - - - - - - rs7523255 1:52163425 T CCDS55598.1 CCDS55598.1 Transcript intron_variant - - - - - - rs7523255 1:52163425 T ENSESTG00000008957 ENSESTT00000022488 Transcript intron_variant - - - - - - rs7523255 1:52163425 T ENSESTG00000008957 ENSESTT00000022600 Transcript intron_variant - - - - - - rs7523255 1:52163425 T ENSESTG00000008957 ENSESTT00000022603 Transcript intron_variant - - - - - - rs7523255 1:52163425 T CCDS41333.2 CCDS41333.2 Transcript intron_variant - - - - - - rs7523255 1:52163425 T 114883 NR_036662.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7523255 1:52163425 T ENSESTG00000008957 ENSESTT00000022596 Transcript intron_variant - - - - - - rs7523255 1:52163425 T ENSESTG00000008957 ENSESTT00000022593 Transcript intron_variant - - - - - - rs7523255 1:52163425 T CCDS44145.1 CCDS44145.1 Transcript intron_variant - - - - - - rs7523255 1:52163425 T 114883 NM_024586.5 Transcript intron_variant - - - - - - rs7523255 1:52163425 T 114883 NM_148908.3 Transcript intron_variant - - - - - - rs7523255 1:52163425 T CCDS41332.3 CCDS41332.3 Transcript intron_variant - - - - - - rs706495 1:52293638 A 4898 NM_001242361.1 Transcript intron_variant - - - - - - rs706495 1:52293638 A 4898 NM_002525.2 Transcript intron_variant - - - - - - rs706495 1:52293638 A CCDS41335.1 CCDS41335.1 Transcript intron_variant - - - - - - rs706495 1:52293638 A ENSESTG00000009180 ENSESTT00000023203 Transcript intron_variant - - - - - - rs706495 1:52293638 A ENSESTG00000009180 ENSESTT00000023178 Transcript intron_variant - - - - - - rs706495 1:52293638 A CCDS55599.1 CCDS55599.1 Transcript intron_variant - - - - - - rs706495 1:52293638 A 4898 NM_001101662.1 Transcript intron_variant - - - - - - rs706495 1:52293638 A CCDS559.1 CCDS559.1 Transcript intron_variant - - - - - - rs706495 1:52293638 A ENSESTG00000009180 ENSESTT00000023198 Transcript intron_variant - - - - - - rs706495 1:52293638 A ENSESTG00000009180 ENSESTT00000023191 Transcript intron_variant - - - - - - rs835031 1:52888937 A 23318 NM_001009881.2 Transcript downstream_gene_variant - - - - - - DISTANCE=10 rs835031 1:52888937 A ENSESTG00000023903 ENSESTT00000060585 Transcript downstream_gene_variant - - - - - - DISTANCE=460 rs835031 1:52888937 A ENSESTG00000023903 ENSESTT00000060489 Transcript downstream_gene_variant - - - - - - DISTANCE=460 rs835031 1:52888937 A CCDS30715.1 CCDS30715.1 Transcript downstream_gene_variant - - - - - - DISTANCE=670 rs835031 1:52888937 A ENSESTG00000023903 ENSESTT00000060694 Transcript intron_variant - - - - - - rs835031 1:52888937 A ENSESTG00000023903 ENSESTT00000060503 Transcript downstream_gene_variant - - - - - - DISTANCE=460 rs835031 1:52888937 A ENSESTG00000023903 ENSESTT00000060615 Transcript downstream_gene_variant - - - - - - DISTANCE=460 rs835031 1:52888937 A ENSESTG00000023903 ENSESTT00000060677 Transcript downstream_gene_variant - - - - - - DISTANCE=383 rs835031 1:52888937 A 84950 NM_032864.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4945 rs835031 1:52888937 A ENSESTG00000023903 ENSESTT00000060592 Transcript downstream_gene_variant - - - - - - DISTANCE=460 rs835031 1:52888937 A ENSESTG00000023903 ENSESTT00000060634 Transcript downstream_gene_variant - - - - - - DISTANCE=460 rs835031 1:52888937 A ENSESTG00000023903 ENSESTT00000060665 Transcript downstream_gene_variant - - - - - - DISTANCE=357 rs835031 1:52888937 A 23318 NM_015269.2 Transcript downstream_gene_variant - - - - - - DISTANCE=10 rs835031 1:52888937 A CCDS30716.1 CCDS30716.1 Transcript downstream_gene_variant - - - - - - DISTANCE=670 rs1288387 1:53539375 T 127435 NM_001199080.1 Transcript intron_variant - - - - - - rs1288387 1:53539375 T ENSESTG00000023200 ENSESTT00000058779 Transcript intron_variant - - - - - - rs1288387 1:53539375 T ENSESTG00000023200 ENSESTT00000058808 Transcript intron_variant - - - - - - rs1288387 1:53539375 T ENSESTG00000023605 ENSESTT00000059510 Transcript intron_variant - - - - - - rs1288387 1:53539375 T CCDS55602.1 CCDS55602.1 Transcript intron_variant - - - - - - rs1288387 1:53539375 T 127435 NM_001199081.1 Transcript intron_variant - - - - - - rs1288387 1:53539375 T ENSESTG00000023200 ENSESTT00000058730 Transcript intron_variant - - - - - - rs1288387 1:53539375 T CCDS573.1 CCDS573.1 Transcript intron_variant - - - - - - rs1288387 1:53539375 T ENSESTG00000023200 ENSESTT00000058803 Transcript intron_variant - - - - - - rs1288387 1:53539375 T ENSESTG00000023200 ENSESTT00000058687 Transcript intron_variant - - - - - - rs1288387 1:53539375 T CCDS55601.1 CCDS55601.1 Transcript intron_variant - - - - - - rs1288387 1:53539375 T ENSESTG00000023200 ENSESTT00000058735 Transcript intron_variant - - - - - - rs1288387 1:53539375 T ENSESTG00000023200 ENSESTT00000058650 Transcript intron_variant - - - - - - rs1288387 1:53539375 T 127435 NM_153703.4 Transcript intron_variant - - - - - - rs1288387 1:53539375 T 127435 NM_001199082.1 Transcript intron_variant - - - - - - rs1288387 1:53539375 T ENSESTG00000023200 ENSESTT00000058787 Transcript intron_variant - - - - - - rs1288395 1:53546173 G 127435 NM_001199080.1 Transcript intron_variant - - - - - - rs1288395 1:53546173 G ENSESTG00000023200 ENSESTT00000058779 Transcript intron_variant - - - - - - rs1288395 1:53546173 G ENSESTG00000023200 ENSESTT00000058808 Transcript intron_variant - - - - - - rs1288395 1:53546173 G ENSESTG00000023605 ENSESTT00000059510 Transcript intron_variant - - - - - - rs1288395 1:53546173 G CCDS55602.1 CCDS55602.1 Transcript intron_variant - - - - - - rs1288395 1:53546173 G 127435 NM_001199081.1 Transcript intron_variant - - - - - - rs1288395 1:53546173 G ENSESTG00000023200 ENSESTT00000058730 Transcript intron_variant - - - - - - rs1288395 1:53546173 G CCDS573.1 CCDS573.1 Transcript intron_variant - - - - - - rs1288395 1:53546173 G ENSESTG00000023200 ENSESTT00000058803 Transcript intron_variant - - - - - - rs1288395 1:53546173 G ENSESTG00000023200 ENSESTT00000058687 Transcript intron_variant - - - - - - rs1288395 1:53546173 G CCDS55601.1 CCDS55601.1 Transcript intron_variant - - - - - - rs1288395 1:53546173 G ENSESTG00000023200 ENSESTT00000058735 Transcript intron_variant - - - - - - rs1288395 1:53546173 G ENSESTG00000023200 ENSESTT00000058650 Transcript intron_variant - - - - - - rs1288395 1:53546173 G 127435 NM_153703.4 Transcript intron_variant - - - - - - rs1288395 1:53546173 G 127435 NM_001199082.1 Transcript intron_variant - - - - - - rs1288395 1:53546173 G ENSESTG00000023200 ENSESTT00000058787 Transcript intron_variant - - - - - - rs10888764 1:53560305 C 6512 NM_006671.4 Transcript intron_variant - - - - - - rs10888764 1:53560305 C ENSESTG00000023571 ENSESTT00000059471 Transcript intron_variant - - - - - - rs10888764 1:53560305 C CCDS574.1 CCDS574.1 Transcript intron_variant - - - - - - rs1288417 1:53563367 C 6512 NM_006671.4 Transcript intron_variant - - - - - - rs1288417 1:53563367 C ENSESTG00000023571 ENSESTT00000059471 Transcript intron_variant - - - - - - rs1288417 1:53563367 C CCDS574.1 CCDS574.1 Transcript intron_variant - - - - - - rs1288364 1:53608375 G 6512 NM_006671.4 Transcript upstream_gene_variant - - - - - - DISTANCE=86 rs1288364 1:53608375 G ENSESTG00000023571 ENSESTT00000059471 Transcript upstream_gene_variant - - - - - - DISTANCE=80 rs1288364 1:53608375 G ENSESTG00000023571 ENSESTT00000059492 Transcript upstream_gene_variant - - - - - - DISTANCE=80 rs1288364 1:53608375 G CCDS574.1 CCDS574.1 Transcript upstream_gene_variant - - - - - - DISTANCE=254 rs4926988 1:53846953 C - - - intergenic_variant - - - - - - rs1300217 1:53906804 G 163742 NR_002314.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1111 rs1288601 1:53907548 T 163742 NR_002314.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1855 rs1288638 1:53936069 G - ENSR00000077218 RegulatoryFeature regulatory_region_variant - - - - - - rs1288638 1:53936069 G 63948 NM_033067.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2911 rs1288638 1:53936069 G ENSESTG00000019574 ENSESTT00000049191 Transcript downstream_gene_variant - - - - - - DISTANCE=2908 rs1288638 1:53936069 G CCDS581.1 CCDS581.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3734 rs1288641 1:53939257 T - ENSR00000670010 RegulatoryFeature regulatory_region_variant - - - - - - rs1288641 1:53939257 T - - - intergenic_variant - - - - - - rs578445 1:54029013 T CCDS582.1 CCDS582.1 Transcript intron_variant - - - - - - rs578445 1:54029013 T 148979 NM_147193.2 Transcript intron_variant - - - - - - rs578445 1:54029013 T ENSESTG00000020491 ENSESTT00000051384 Transcript intron_variant - - - - - - rs727418 1:54435551 A ENSESTG00000019717 ENSESTT00000049472 Transcript downstream_gene_variant - - - - - - DISTANCE=1712 rs727418 1:54435551 A 115353 NM_052940.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1710 rs727418 1:54435551 A 115353 NM_001256409.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1710 rs727418 1:54435551 A CCDS585.1 CCDS585.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1939 rs1883451 1:54437569 C - ENSR00000536784 RegulatoryFeature regulatory_region_variant - - - - - - rs1883451 1:54437569 C ENSESTG00000019717 ENSESTT00000049472 Transcript downstream_gene_variant - - - - - - DISTANCE=3730 rs1883451 1:54437569 C 115353 NM_052940.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3728 rs1883451 1:54437569 C 115353 NM_001256409.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3728 rs1883451 1:54437569 C CCDS585.1 CCDS585.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3957 rs1181086 1:54509644 C ENSESTG00000020078 ENSESTT00000050447 Transcript intron_variant - - - - - - rs1181086 1:54509644 C ENSESTG00000020078 ENSESTT00000050476 Transcript intron_variant - - - - - - rs1181086 1:54509644 C CCDS586.1 CCDS586.1 Transcript intron_variant - - - - - - rs1181086 1:54509644 C ENSESTG00000020078 ENSESTT00000050488 Transcript intron_variant - - - - - - rs1181086 1:54509644 C 9528 NM_004872.3 Transcript intron_variant - - - - - - rs1181087 1:54526899 C 127428 NM_153035.1 Transcript intron_variant - - - - - - rs1181087 1:54526899 C CCDS587.1 CCDS587.1 Transcript intron_variant - - - - - - rs1181087 1:54526899 C ENSESTG00000019750 ENSESTT00000049566 Transcript intron_variant - - - - - - rs1181087 1:54526899 C ENSESTG00000020070 ENSESTT00000050294 Transcript intron_variant - - - - - - rs584891 1:54622929 C CCDS588.2 CCDS588.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4334 rs584891 1:54622929 C 200008 NM_201546.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3486 rs649201 1:54625566 G - - - intergenic_variant - - - - - - rs10788983 1:55019343 A 26027 NM_147161.3 Transcript intron_variant - - - - - - rs10788983 1:55019343 A ENSESTG00000015121 ENSESTT00000037948 Transcript intron_variant - - - - - - rs10788983 1:55019343 A CCDS593.1 CCDS593.1 Transcript intron_variant - - - - - - rs10788983 1:55019343 A ENSESTG00000015121 ENSESTT00000037929 Transcript intron_variant - - - - - - rs10788983 1:55019343 A 26027 NM_015547.3 Transcript intron_variant - - - - - - rs10788983 1:55019343 A ENSESTG00000015121 ENSESTT00000037939 Transcript intron_variant - - - - - - rs10788983 1:55019343 A CCDS592.1 CCDS592.1 Transcript intron_variant - - - - - - rs300282 1:55032986 C 26027 NM_147161.3 Transcript intron_variant - - - - - - rs300282 1:55032986 C ENSESTG00000015121 ENSESTT00000037985 Transcript intron_variant - - - - - - rs300282 1:55032986 C ENSESTG00000015121 ENSESTT00000037948 Transcript intron_variant - - - - - - rs300282 1:55032986 C CCDS593.1 CCDS593.1 Transcript intron_variant - - - - - - rs300282 1:55032986 C ENSESTG00000015121 ENSESTT00000037929 Transcript intron_variant - - - - - - rs300282 1:55032986 C 26027 NM_015547.3 Transcript intron_variant - - - - - - rs300282 1:55032986 C ENSESTG00000015121 ENSESTT00000037939 Transcript intron_variant - - - - - - rs300282 1:55032986 C CCDS592.1 CCDS592.1 Transcript intron_variant - - - - - - rs300282 1:55032986 C ENSESTG00000015121 ENSESTT00000037954 Transcript intron_variant - - - - - - rs300282 1:55032986 C ENSESTG00000015121 ENSESTT00000037964 Transcript intron_variant - - - - - - rs655337 1:55124718 G 100527960 NR_037639.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs655337 1:55124718 G ENSESTG00000015121 ENSESTT00000038195 Transcript intron_variant - - - - - - rs655337 1:55124718 G CCDS41342.2 CCDS41342.2 Transcript intron_variant - - - - - - rs655337 1:55124718 G 374977 NR_026782.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs655337 1:55124718 G ENSESTG00000015121 ENSESTT00000038083 Transcript intron_variant - - - - - - rs655337 1:55124718 G 100527960 NR_037640.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs655337 1:55124718 G ENSESTG00000015121 ENSESTT00000038176 Transcript intron_variant - - - - - - rs655337 1:55124718 G ENSESTG00000015121 ENSESTT00000038105 Transcript intron_variant - - - - - - rs655337 1:55124718 G ENSESTG00000015121 ENSESTT00000038184 Transcript intron_variant - - - - - - rs655337 1:55124718 G ENSESTG00000015121 ENSESTT00000038130 Transcript intron_variant - - - - - - rs655337 1:55124718 G 100527960 NR_037641.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs655337 1:55124718 G 374977 NM_001039464.2 Transcript intron_variant - - - - - - rs665118 1:55253575 C CCDS44152.1 CCDS44152.1 Transcript intron_variant - - - - - - rs665118 1:55253575 C 55001 NM_001114108.1 Transcript intron_variant - - - - - - rs665118 1:55253575 C ENSESTG00000015523 ENSESTT00000038875 Transcript downstream_gene_variant - - - - - - DISTANCE=149 rs665118 1:55253575 C ENSESTG00000015336 ENSESTT00000038411 Transcript upstream_gene_variant - - - - - - DISTANCE=4982 rs665118 1:55253575 C CCDS598.1 CCDS598.1 Transcript intron_variant - - - - - - rs665118 1:55253575 C 55001 NM_017904.3 Transcript intron_variant - - - - - - rs602152 1:55258478 C CCDS44152.1 CCDS44152.1 Transcript intron_variant - - - - - - rs602152 1:55258478 C 55001 NM_001114108.1 Transcript intron_variant - - - - - - rs602152 1:55258478 C ENSESTG00000015523 ENSESTT00000038875 Transcript intron_variant - - - - - - rs602152 1:55258478 C ENSESTG00000015336 ENSESTT00000038411 Transcript upstream_gene_variant - - - - - - DISTANCE=79 rs602152 1:55258478 C CCDS598.1 CCDS598.1 Transcript intron_variant - - - - - - rs602152 1:55258478 C 55001 NM_017904.3 Transcript intron_variant - - - - - - rs584085 1:55274834 C - ENSR00000670049 RegulatoryFeature regulatory_region_variant - - - - - - rs584085 1:55274834 C CCDS599.1 CCDS599.1 Transcript intron_variant - - - - - - rs584085 1:55274834 C ENSESTG00000015342 ENSESTT00000038433 Transcript intron_variant - - - - - - rs584085 1:55274834 C 163747 NM_001110533.1 Transcript intron_variant - - - - - - rs584085 1:55274834 C CCDS44153.1 CCDS44153.1 Transcript intron_variant - - - - - - rs584085 1:55274834 C 163747 NM_152607.2 Transcript intron_variant - - - - - - rs600499 1:55277599 C CCDS599.1 CCDS599.1 Transcript missense_variant 613 613 205 Y/H Tat/Cat - PolyPhen=benign;SIFT=tolerated rs600499 1:55277599 C ENSESTG00000015342 ENSESTT00000038433 Transcript downstream_gene_variant - - - - - - DISTANCE=63 rs600499 1:55277599 C 163747 NM_001110533.1 Transcript missense_variant 667 613 205 Y/H Tat/Cat - PolyPhen=benign;SIFT=tolerated rs600499 1:55277599 C ENSESTG00000015355 ENSESTT00000038439 Transcript upstream_gene_variant - - - - - - DISTANCE=3024 rs600499 1:55277599 C CCDS44153.1 CCDS44153.1 Transcript missense_variant 613 613 205 Y/H Tat/Cat - PolyPhen=benign;SIFT=tolerated rs600499 1:55277599 C 163747 NM_152607.2 Transcript missense_variant 667 613 205 Y/H Tat/Cat - PolyPhen=benign;SIFT=tolerated rs668424 1:55282079 C CCDS599.1 CCDS599.1 Transcript intron_variant - - - - - - rs668424 1:55282079 C ENSESTG00000015342 ENSESTT00000038433 Transcript downstream_gene_variant - - - - - - DISTANCE=4543 rs668424 1:55282079 C 163747 NM_001110533.1 Transcript intron_variant - - - - - - rs668424 1:55282079 C ENSESTG00000015355 ENSESTT00000038439 Transcript intron_variant - - - - - - rs668424 1:55282079 C CCDS44153.1 CCDS44153.1 Transcript intron_variant - - - - - - rs668424 1:55282079 C 163747 NM_152607.2 Transcript intron_variant - - - - - - rs633102 1:55303463 G ENSESTG00000015483 ENSESTT00000038863 Transcript intron_variant - - - - - - rs633102 1:55303463 G CCDS599.1 CCDS599.1 Transcript intron_variant - - - - - - rs633102 1:55303463 G 163747 NM_001110533.1 Transcript intron_variant - - - - - - rs633102 1:55303463 G ENSESTG00000015355 ENSESTT00000038439 Transcript intron_variant - - - - - - rs633102 1:55303463 G CCDS44153.1 CCDS44153.1 Transcript intron_variant - - - - - - rs633102 1:55303463 G 163747 NM_152607.2 Transcript intron_variant - - - - - - rs594688 1:55313382 C CCDS600.1 CCDS600.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4524 rs594688 1:55313382 C 1718 NM_014762.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1918 rs594688 1:55313382 C ENSESTG00000015483 ENSESTT00000038863 Transcript intron_variant - - - - - - rs594688 1:55313382 C ENSESTG00000015483 ENSESTT00000038776 Transcript downstream_gene_variant - - - - - - DISTANCE=3539 rs657688 1:55315351 C CCDS600.1 CCDS600.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2555 rs657688 1:55315351 C 1718 NM_014762.3 Transcript 3_prime_UTR_variant 4235 - - - - - rs657688 1:55315351 C ENSESTG00000015483 ENSESTT00000038863 Transcript intron_variant - - - - - - rs657688 1:55315351 C ENSESTG00000015483 ENSESTT00000038869 Transcript downstream_gene_variant - - - - - - DISTANCE=4503 rs657688 1:55315351 C ENSESTG00000015483 ENSESTT00000038776 Transcript downstream_gene_variant - - - - - - DISTANCE=1570 rs640011 1:55332774 C - ENSR00001520391 RegulatoryFeature regulatory_region_variant - - - - - - rs640011 1:55332774 C CCDS600.1 CCDS600.1 Transcript intron_variant - - - - - - rs640011 1:55332774 C 1718 NM_014762.3 Transcript intron_variant - - - - - - rs640011 1:55332774 C ENSESTG00000015483 ENSESTT00000038863 Transcript intron_variant - - - - - - rs640011 1:55332774 C ENSESTG00000015483 ENSESTT00000038869 Transcript intron_variant - - - - - - rs640011 1:55332774 C ENSESTG00000015483 ENSESTT00000038776 Transcript intron_variant - - - - - - rs659161 1:55337540 C CCDS600.1 CCDS600.1 Transcript intron_variant - - - - - - rs659161 1:55337540 C 1718 NM_014762.3 Transcript intron_variant - - - - - - rs659161 1:55337540 C ENSESTG00000015483 ENSESTT00000038863 Transcript intron_variant - - - - - - rs659161 1:55337540 C ENSESTG00000015483 ENSESTT00000038869 Transcript intron_variant - - - - - - rs659161 1:55337540 C ENSESTG00000015483 ENSESTT00000038776 Transcript intron_variant - - - - - - rs680922 1:55348191 A - ENSR00000536939 RegulatoryFeature regulatory_region_variant - - - - - - rs680922 1:55348191 A CCDS600.1 CCDS600.1 Transcript intron_variant - - - - - - rs680922 1:55348191 A 1718 NM_014762.3 Transcript intron_variant - - - - - - rs680922 1:55348191 A ENSESTG00000015483 ENSESTT00000038863 Transcript intron_variant - - - - - - rs680922 1:55348191 A ENSESTG00000015483 ENSESTT00000038869 Transcript intron_variant - - - - - - rs680922 1:55348191 A ENSESTG00000015483 ENSESTT00000038776 Transcript intron_variant - - - - - - rs680922 1:55348191 A ENSESTG00000015358 ENSESTT00000038452 Transcript upstream_gene_variant - - - - - - DISTANCE=4351 rs612798 1:55364720 G - - - intergenic_variant - - - - - - rs2500320 1:55441676 A ENSESTG00000015372 ENSESTT00000038506 Transcript upstream_gene_variant - - - - - - DISTANCE=4789 rs2500320 1:55441676 A 199964 NM_182532.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4789 rs2500320 1:55441676 A ENSESTG00000015478 ENSESTT00000038737 Transcript downstream_gene_variant - - - - - - DISTANCE=4947 rs1499660 1:56019059 G - - - intergenic_variant - - - - - - rs1499673 1:56034239 A - - - intergenic_variant - - - - - - rs1165463 1:56083655 T - - - intergenic_variant - - - - - - rs769967 1:56092580 G - - - intergenic_variant - - - - - - rs769996 1:56095782 C - - - intergenic_variant - - - - - - rs769975 1:56114431 C - - - intergenic_variant - - - - - - rs1165477 1:56172876 T - - - intergenic_variant - - - - - - rs3118511 1:56242730 G - - - intergenic_variant - - - - - - rs4244654 1:56431133 A - - - intergenic_variant - - - - - - rs1341342 1:56733040 C - - - intergenic_variant - - - - - - rs2249018 1:57074261 C - - - intergenic_variant - - - - - - rs2796515 1:57152121 A - ENSR00000537254 RegulatoryFeature regulatory_region_variant - - - - - - rs2796515 1:57152121 A ENSESTG00000011354 ENSESTT00000028512 Transcript intron_variant - - - - - - rs2796515 1:57152121 A ENSESTG00000011354 ENSESTT00000028523 Transcript intron_variant - - - - - - rs2796515 1:57152121 A ENSESTG00000011354 ENSESTT00000028521 Transcript intron_variant - - - - - - rs2796515 1:57152121 A CCDS605.1 CCDS605.1 Transcript intron_variant - - - - - - rs2796515 1:57152121 A 5563 NM_006252.3 Transcript intron_variant - - - - - - rs2405235 1:57274467 T CCDS30729.1 CCDS30729.1 Transcript intron_variant - - - - - - rs2405235 1:57274467 T 199920 NM_001004303.4 Transcript intron_variant - - - - - - rs639465 1:57460280 T 1600 NM_021080.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3299 rs532954 1:57604914 T ENSESTG00000011388 ENSESTT00000028625 Transcript intron_variant - - - - - - rs532954 1:57604914 T ENSESTG00000011388 ENSESTT00000028608 Transcript intron_variant - - - - - - rs532954 1:57604914 T CCDS607.1 CCDS607.1 Transcript intron_variant - - - - - - rs532954 1:57604914 T ENSESTG00000011388 ENSESTT00000028615 Transcript intron_variant - - - - - - rs532954 1:57604914 T 1600 NM_021080.3 Transcript intron_variant - - - - - - rs662134 1:57757692 G ENSESTG00000011388 ENSESTT00000028625 Transcript intron_variant - - - - - - rs662134 1:57757692 G ENSESTG00000011388 ENSESTT00000028608 Transcript intron_variant - - - - - - rs662134 1:57757692 G CCDS607.1 CCDS607.1 Transcript upstream_gene_variant - - - - - - DISTANCE=990 rs662134 1:57757692 G ENSESTG00000011388 ENSESTT00000028615 Transcript intron_variant - - - - - - rs662134 1:57757692 G 1600 NM_021080.3 Transcript intron_variant - - - - - - rs912362 1:58193097 G 1600 NM_021080.3 Transcript intron_variant - - - - - - rs2406277 1:58211873 G 1600 NM_021080.3 Transcript intron_variant - - - - - - rs539266 1:58647820 C 1600 NM_021080.3 Transcript intron_variant - - - - - - rs552131 1:58660204 A 1600 NM_021080.3 Transcript intron_variant - - - - - - rs681213 1:60461675 G ENSESTG00000020884 ENSESTT00000052352 Transcript intron_variant - - - - - - rs681213 1:60461675 G CCDS614.1 CCDS614.1 Transcript intron_variant - - - - - - rs681213 1:60461675 G ENSESTG00000020884 ENSESTT00000052393 Transcript intron_variant - - - - - - rs681213 1:60461675 G 127795 NM_152377.2 Transcript intron_variant - - - - - - rs1759683 1:60574824 T - - - intergenic_variant - - - - - - rs4390204 1:60954599 T - - - intergenic_variant - - - - - - rs4244168 1:60980196 T - ENSR00000670144 RegulatoryFeature regulatory_region_variant - - - - - - rs4244168 1:60980196 T - - - intergenic_variant - - - - - - rs4916069 1:61012449 G - - - intergenic_variant - - - - - - rs2474392 1:61851446 A ENSESTG00000008218 ENSESTT00000020765 Transcript intron_variant - - - - - - rs2474392 1:61851446 A 4774 NM_005595.4 Transcript intron_variant - - - - - - rs2474392 1:61851446 A ENSESTG00000008232 ENSESTT00000020787 Transcript intron_variant - - - - - - rs2474392 1:61851446 A 4774 NM_001134673.3 Transcript intron_variant - - - - - - rs2474392 1:61851446 A 4774 NM_001145511.1 Transcript intron_variant - - - - - - rs2474392 1:61851446 A CCDS53321.1 CCDS53321.1 Transcript intron_variant - - - - - - rs2474392 1:61851446 A ENSESTG00000001258 ENSESTT00000002972 Transcript downstream_gene_variant - - - - - - DISTANCE=2438 rs2474392 1:61851446 A CCDS615.1 CCDS615.1 Transcript intron_variant - - - - - - rs2474392 1:61851446 A 4774 NM_001145512.1 Transcript intron_variant - - - - - - rs2474392 1:61851446 A CCDS53322.1 CCDS53322.1 Transcript intron_variant - - - - - - rs2474392 1:61851446 A CCDS44156.1 CCDS44156.1 Transcript intron_variant - - - - - - rs2499545 1:61856839 C ENSESTG00000008218 ENSESTT00000020765 Transcript intron_variant - - - - - - rs2499545 1:61856839 C 4774 NM_005595.4 Transcript intron_variant - - - - - - rs2499545 1:61856839 C ENSESTG00000008232 ENSESTT00000020787 Transcript intron_variant - - - - - - rs2499545 1:61856839 C 4774 NM_001134673.3 Transcript intron_variant - - - - - - rs2499545 1:61856839 C 4774 NM_001145511.1 Transcript intron_variant - - - - - - rs2499545 1:61856839 C CCDS53321.1 CCDS53321.1 Transcript intron_variant - - - - - - rs2499545 1:61856839 C CCDS615.1 CCDS615.1 Transcript intron_variant - - - - - - rs2499545 1:61856839 C 4774 NM_001145512.1 Transcript intron_variant - - - - - - rs2499545 1:61856839 C CCDS53322.1 CCDS53322.1 Transcript intron_variant - - - - - - rs2499545 1:61856839 C CCDS44156.1 CCDS44156.1 Transcript intron_variant - - - - - - rs4915601 1:62428912 C 10207 NM_176877.2 Transcript intron_variant - - - - - - rs4915601 1:62428912 C ENSESTG00000001269 ENSESTT00000003121 Transcript intron_variant - - - - - - rs4915601 1:62428912 C CCDS617.2 CCDS617.2 Transcript intron_variant - - - - - - rs4915601 1:62428912 C ENSESTG00000001269 ENSESTT00000003102 Transcript intron_variant - - - - - - rs4915601 1:62428912 C ENSESTG00000001269 ENSESTT00000003079 Transcript intron_variant - - - - - - rs658897 1:62912247 T ENSESTG00000009239 ENSESTT00000023234 Transcript intron_variant - - - - - - rs658897 1:62912247 T CCDS621.1 CCDS621.1 Transcript intron_variant - - - - - - rs658897 1:62912247 T ENSESTG00000009239 ENSESTT00000023213 Transcript intron_variant - - - - - - rs658897 1:62912247 T 7398 NM_001017416.1 Transcript intron_variant - - - - - - rs658897 1:62912247 T 7398 NM_001017415.1 Transcript intron_variant - - - - - - rs658897 1:62912247 T ENSESTG00000009239 ENSESTT00000023227 Transcript intron_variant - - - - - - rs658897 1:62912247 T 7398 NM_003368.4 Transcript intron_variant - - - - - - rs658897 1:62912247 T ENSESTG00000009239 ENSESTT00000023255 Transcript upstream_gene_variant - - - - - - DISTANCE=1887 rs1168011 1:62945933 G CCDS30734.1 CCDS30734.1 Transcript intron_variant - - - - - - rs1168011 1:62945933 G 85440 NM_033407.2 Transcript intron_variant - - - - - - rs1168011 1:62945933 G ENSESTG00000009510 ENSESTT00000023913 Transcript intron_variant - - - - - - rs1359332 1:63081916 C CCDS30734.1 CCDS30734.1 Transcript intron_variant - - - - - - rs1359332 1:63081916 C 85440 NM_033407.2 Transcript intron_variant - - - - - - rs1359332 1:63081916 C ENSESTG00000009406 ENSESTT00000023624 Transcript intron_variant - - - - - - rs1359332 1:63081916 C ENSESTG00000009406 ENSESTT00000023619 Transcript intron_variant - - - - - - rs1168096 1:63120053 C CCDS30734.1 CCDS30734.1 Transcript intron_variant - - - - - - rs1168096 1:63120053 C ENSESTG00000009394 ENSESTT00000023549 Transcript intron_variant - - - - - - rs1168096 1:63120053 C 85440 NM_033407.2 Transcript intron_variant - - - - - - rs2367043 1:63493304 C - - - intergenic_variant - - - - - - rs1032661 1:63520797 C - - - intergenic_variant - - - - - - rs2658438 1:64207260 G - - - intergenic_variant - - - - - - rs2658437 1:64208103 C - - - intergenic_variant - - - - - - rs855830 1:64370282 C 4919 NM_001083592.1 Transcript intron_variant - - - - - - rs855830 1:64370282 C CCDS41344.1 CCDS41344.1 Transcript intron_variant - - - - - - rs855830 1:64370282 C ENSESTG00000006133 ENSESTT00000015456 Transcript intron_variant - - - - - - rs855830 1:64370282 C CCDS626.1 CCDS626.1 Transcript intron_variant - - - - - - rs855830 1:64370282 C 4919 NM_005012.3 Transcript intron_variant - - - - - - rs1496029 1:64827962 G - - - intergenic_variant - - - - - - rs4915974 1:64842263 T - - - intergenic_variant - - - - - - rs1469875 1:65060890 A 57685 NM_020925.2 Transcript intron_variant - - - - - - rs1469875 1:65060890 A ENSESTG00000000005 ENSESTT00000000007 Transcript intron_variant - - - - - - rs1469875 1:65060890 A CCDS628.2 CCDS628.2 Transcript intron_variant - - - - - - rs1469875 1:65060890 A ENSESTG00000000005 ENSESTT00000000006 Transcript intron_variant - - - - - - rs1469875 1:65060890 A ENSESTG00000000005 ENSESTT00000000008 Transcript intron_variant - - - - - - rs77510607 1:65339919 A ENSESTG00000000010 ENSESTT00000000029 Transcript downstream_gene_variant - - - - - - DISTANCE=1716 rs77510607 1:65339919 A ENSESTG00000000010 ENSESTT00000000028 Transcript intron_variant - - - - - - rs77510607 1:65339919 A ENSESTG00000000010 ENSESTT00000000026 Transcript intron_variant - - - - - - rs77510607 1:65339919 A 3716 NM_002227.2 Transcript intron_variant - - - - - - rs77510607 1:65339919 A CCDS41346.1 CCDS41346.1 Transcript intron_variant - - - - - - rs77510607 1:65339919 A ENSESTG00000000010 ENSESTT00000000030 Transcript intron_variant - - - - - - rs77510607 1:65339919 A ENSESTG00000000010 ENSESTT00000000027 Transcript intron_variant - - - - - - rs310203 1:65348485 C - ENSR00000538206 RegulatoryFeature regulatory_region_variant - - - - - - rs310203 1:65348485 C ENSESTG00000000010 ENSESTT00000000029 Transcript intron_variant - - - - - - rs310203 1:65348485 C ENSESTG00000000010 ENSESTT00000000028 Transcript intron_variant - - - - - - rs310203 1:65348485 C ENSESTG00000000010 ENSESTT00000000026 Transcript intron_variant - - - - - - rs310203 1:65348485 C 3716 NM_002227.2 Transcript intron_variant - - - - - - rs310203 1:65348485 C CCDS41346.1 CCDS41346.1 Transcript intron_variant - - - - - - rs310203 1:65348485 C ENSESTG00000000010 ENSESTT00000000030 Transcript intron_variant - - - - - - rs310203 1:65348485 C ENSESTG00000000010 ENSESTT00000000027 Transcript intron_variant - - - - - - rs693239 1:65516410 G ENSESTG00000000010 ENSESTT00000000026 Transcript intron_variant - - - - - - rs6588123 1:65610837 C 205 NM_013410.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3013 rs6588123 1:65610837 C ENSESTG00000000007 ENSESTT00000000016 Transcript upstream_gene_variant - - - - - - DISTANCE=3013 rs6588123 1:65610837 C 205 NM_203464.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2395 rs6588123 1:65610837 C ENSESTG00000000007 ENSESTT00000000014 Transcript upstream_gene_variant - - - - - - DISTANCE=2395 rs6588123 1:65610837 C CCDS629.1 CCDS629.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3254 rs6588123 1:65610837 C ENSESTG00000000007 ENSESTT00000000015 Transcript upstream_gene_variant - - - - - - DISTANCE=2708 rs6588123 1:65610837 C 205 NM_001005353.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2676 rs2186248 1:66036501 T 3953 NM_001003679.3 Transcript intron_variant - - - - - - rs2186248 1:66036501 T CCDS631.1 CCDS631.1 Transcript intron_variant - - - - - - rs2186248 1:66036501 T CCDS30741.1 CCDS30741.1 Transcript intron_variant - - - - - - rs2186248 1:66036501 T CCDS30740.1 CCDS30740.1 Transcript intron_variant - - - - - - rs2186248 1:66036501 T ENSESTG00000014916 ENSESTT00000037514 Transcript intron_variant - - - - - - rs2186248 1:66036501 T ENSESTG00000014916 ENSESTT00000037485 Transcript intron_variant - - - - - - rs2186248 1:66036501 T 3953 NM_002303.5 Transcript intron_variant - - - - - - rs2186248 1:66036501 T ENSESTG00000014916 ENSESTT00000037495 Transcript intron_variant - - - - - - rs2186248 1:66036501 T ENSESTG00000014916 ENSESTT00000037556 Transcript intron_variant - - - - - - rs2186248 1:66036501 T ENSESTG00000014916 ENSESTT00000037564 Transcript intron_variant - - - - - - rs2186248 1:66036501 T ENSESTG00000014916 ENSESTT00000037569 Transcript intron_variant - - - - - - rs2186248 1:66036501 T 3953 NM_001198688.1 Transcript intron_variant - - - - - - rs2186248 1:66036501 T CCDS55604.1 CCDS55604.1 Transcript intron_variant - - - - - - rs2186248 1:66036501 T 3953 NM_001198687.1 Transcript intron_variant - - - - - - rs2186248 1:66036501 T 3953 NM_001198689.1 Transcript intron_variant - - - - - - rs2186248 1:66036501 T ENSESTG00000014916 ENSESTT00000037519 Transcript intron_variant - - - - - - rs2186248 1:66036501 T ENSESTG00000014916 ENSESTT00000037548 Transcript intron_variant - - - - - - rs2186248 1:66036501 T 3953 NM_001003680.3 Transcript intron_variant - - - - - - rs6683810 1:66281348 C 5142 NM_002600.3 Transcript intron_variant - - - - - - rs6683810 1:66281348 C ENSESTG00000015011 ENSESTT00000037599 Transcript intron_variant - - - - - - rs6683810 1:66281348 C 5142 NM_001037341.1 Transcript intron_variant - - - - - - rs2455029 1:66539445 T CCDS632.1 CCDS632.1 Transcript intron_variant - - - - - - rs2455029 1:66539445 T 5142 NM_002600.3 Transcript intron_variant - - - - - - rs2455029 1:66539445 T 5142 NM_001037340.1 Transcript intron_variant - - - - - - rs2455029 1:66539445 T ENSESTG00000015021 ENSESTT00000037638 Transcript intron_variant - - - - - - rs2455029 1:66539445 T ENSESTG00000015021 ENSESTT00000037643 Transcript intron_variant - - - - - - rs2455029 1:66539445 T ENSESTG00000015021 ENSESTT00000037649 Transcript intron_variant - - - - - - rs2455029 1:66539445 T CCDS30742.1 CCDS30742.1 Transcript intron_variant - - - - - - rs2455029 1:66539445 T 5142 NM_001037341.1 Transcript intron_variant - - - - - - rs2455027 1:66557944 G CCDS632.1 CCDS632.1 Transcript intron_variant - - - - - - rs2455027 1:66557944 G 5142 NM_002600.3 Transcript intron_variant - - - - - - rs2455027 1:66557944 G 5142 NM_001037340.1 Transcript intron_variant - - - - - - rs2455027 1:66557944 G ENSESTG00000015021 ENSESTT00000037638 Transcript intron_variant - - - - - - rs2455027 1:66557944 G ENSESTG00000015021 ENSESTT00000037643 Transcript intron_variant - - - - - - rs2455027 1:66557944 G ENSESTG00000015021 ENSESTT00000037649 Transcript intron_variant - - - - - - rs2455027 1:66557944 G CCDS30742.1 CCDS30742.1 Transcript intron_variant - - - - - - rs2455027 1:66557944 G 5142 NM_001037341.1 Transcript intron_variant - - - - - - rs2485385 1:66581469 T CCDS632.1 CCDS632.1 Transcript intron_variant - - - - - - rs2485385 1:66581469 T 5142 NM_002600.3 Transcript intron_variant - - - - - - rs2485385 1:66581469 T 5142 NM_001037340.1 Transcript intron_variant - - - - - - rs2485385 1:66581469 T ENSESTG00000015021 ENSESTT00000037638 Transcript intron_variant - - - - - - rs2485385 1:66581469 T ENSESTG00000015021 ENSESTT00000037643 Transcript intron_variant - - - - - - rs2485385 1:66581469 T ENSESTG00000015021 ENSESTT00000037649 Transcript downstream_gene_variant - - - - - - DISTANCE=2988 rs2485385 1:66581469 T CCDS30742.1 CCDS30742.1 Transcript intron_variant - - - - - - rs2485385 1:66581469 T 5142 NM_001037341.1 Transcript intron_variant - - - - - - rs2503168 1:66583378 C CCDS632.1 CCDS632.1 Transcript intron_variant - - - - - - rs2503168 1:66583378 C 5142 NM_002600.3 Transcript intron_variant - - - - - - rs2503168 1:66583378 C 5142 NM_001037340.1 Transcript intron_variant - - - - - - rs2503168 1:66583378 C ENSESTG00000015021 ENSESTT00000037638 Transcript intron_variant - - - - - - rs2503168 1:66583378 C ENSESTG00000015021 ENSESTT00000037643 Transcript intron_variant - - - - - - rs2503168 1:66583378 C ENSESTG00000015021 ENSESTT00000037649 Transcript downstream_gene_variant - - - - - - DISTANCE=4897 rs2503168 1:66583378 C CCDS30742.1 CCDS30742.1 Transcript intron_variant - - - - - - rs2503168 1:66583378 C 5142 NM_001037341.1 Transcript intron_variant - - - - - - rs2485388 1:66585768 G CCDS632.1 CCDS632.1 Transcript intron_variant - - - - - - rs2485388 1:66585768 G 5142 NM_002600.3 Transcript intron_variant - - - - - - rs2485388 1:66585768 G 5142 NM_001037340.1 Transcript intron_variant - - - - - - rs2485388 1:66585768 G CCDS30742.1 CCDS30742.1 Transcript intron_variant - - - - - - rs2485388 1:66585768 G ENSESTG00000015021 ENSESTT00000037638 Transcript intron_variant - - - - - - rs2485388 1:66585768 G 5142 NM_001037341.1 Transcript intron_variant - - - - - - rs2485388 1:66585768 G ENSESTG00000015021 ENSESTT00000037643 Transcript intron_variant - - - - - - rs2485386 1:66593964 A CCDS632.1 CCDS632.1 Transcript intron_variant - - - - - - rs2485386 1:66593964 A 5142 NM_002600.3 Transcript intron_variant - - - - - - rs2485386 1:66593964 A 5142 NM_001037340.1 Transcript intron_variant - - - - - - rs2485386 1:66593964 A CCDS30742.1 CCDS30742.1 Transcript intron_variant - - - - - - rs2485386 1:66593964 A ENSESTG00000015021 ENSESTT00000037638 Transcript intron_variant - - - - - - rs2485386 1:66593964 A 5142 NM_001037341.1 Transcript intron_variant - - - - - - rs2485386 1:66593964 A ENSESTG00000015021 ENSESTT00000037643 Transcript intron_variant - - - - - - rs2503171 1:66599898 G CCDS632.1 CCDS632.1 Transcript intron_variant - - - - - - rs2503171 1:66599898 G 5142 NM_002600.3 Transcript intron_variant - - - - - - rs2503171 1:66599898 G 5142 NM_001037340.1 Transcript intron_variant - - - - - - rs2503171 1:66599898 G CCDS30742.1 CCDS30742.1 Transcript intron_variant - - - - - - rs2503171 1:66599898 G ENSESTG00000015021 ENSESTT00000037638 Transcript intron_variant - - - - - - rs2503171 1:66599898 G 5142 NM_001037341.1 Transcript intron_variant - - - - - - rs2503171 1:66599898 G ENSESTG00000015021 ENSESTT00000037643 Transcript intron_variant - - - - - - rs783577 1:67025193 T ENSESTG00000027475 ENSESTT00000069315 Transcript intron_variant - - - - - - rs783577 1:67025193 T CCDS30744.1 CCDS30744.1 Transcript intron_variant - - - - - - rs783577 1:67025193 T ENSESTG00000027475 ENSESTT00000069336 Transcript intron_variant - - - - - - rs783577 1:67025193 T 84251 NM_032291.2 Transcript intron_variant - - - - - - rs783577 1:67025193 T ENSESTG00000027475 ENSESTT00000069385 Transcript intron_variant - - - - - - rs783577 1:67025193 T ENSESTG00000027475 ENSESTT00000069281 Transcript intron_variant - - - - - - rs783577 1:67025193 T ENSESTG00000027475 ENSESTT00000069292 Transcript intron_variant - - - - - - rs2985814 1:67384337 T ENSESTG00000027687 ENSESTT00000069703 Transcript upstream_gene_variant - - - - - - DISTANCE=4167 rs2985814 1:67384337 T ENSESTG00000027907 ENSESTT00000070341 Transcript intron_variant - - - - - - rs2985814 1:67384337 T 79819 NM_207014.2 Transcript intron_variant - - - - - - rs2985814 1:67384337 T CCDS635.1 CCDS635.1 Transcript intron_variant - - - - - - rs2985814 1:67384337 T 79819 NM_024763.4 Transcript intron_variant - - - - - - rs2985814 1:67384337 T ENSESTG00000027907 ENSESTT00000070364 Transcript intron_variant - - - - - - rs2985814 1:67384337 T CCDS44157.1 CCDS44157.1 Transcript intron_variant - - - - - - rs10889695 1:67954586 G - - - intergenic_variant - - - - - - rs589341 1:68190909 C - ENSR00001521366 RegulatoryFeature regulatory_region_variant - - - - - - rs589341 1:68190909 C ENSESTG00000031194 ENSESTT00000078608 Transcript intron_variant - - - - - - rs589341 1:68190909 C 55970 NM_018841.5 Transcript intron_variant - - - - - - rs589341 1:68190909 C ENSESTG00000031194 ENSESTT00000078652 Transcript intron_variant - - - - - - rs4655572 1:68369612 G 100289178 NR_040077.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4655572 1:68369612 G ENSESTG00000031037 ENSESTT00000078096 Transcript intron_variant - - - - - - rs7526611 1:68386457 C 100289178 NR_040077.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs269357 1:68528553 T 100289178 NR_040077.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3125901 1:68903165 A ENSESTG00000017290 ENSESTT00000043435 Transcript intron_variant - - - - - - rs3125901 1:68903165 A 6121 NM_000329.2 Transcript intron_variant - - - - - - rs3125901 1:68903165 A ENSESTG00000017253 ENSESTT00000043402 Transcript downstream_gene_variant - - - - - - DISTANCE=1815 rs3125901 1:68903165 A CCDS643.1 CCDS643.1 Transcript intron_variant - - - - - - rs3125901 1:68903165 A ENSESTG00000017253 ENSESTT00000043348 Transcript downstream_gene_variant - - - - - - DISTANCE=3437 rs9436861 1:69395432 T - - - intergenic_variant - - - - - - rs1631668 1:69664909 C - - - intergenic_variant - - - - - - rs4501789 1:69675116 T - - - intergenic_variant - - - - - - rs2815448 1:69814353 A - - - intergenic_variant - - - - - - rs1749490 1:70090223 G ENSESTG00000005485 ENSESTT00000013962 Transcript intron_variant - - - - - - rs1749490 1:70090223 G ENSESTG00000005485 ENSESTT00000013971 Transcript intron_variant - - - - - - rs1615997 1:70160752 G ENSESTG00000005485 ENSESTT00000013962 Transcript intron_variant - - - - - - rs1615997 1:70160752 G ENSESTG00000005485 ENSESTT00000013971 Transcript intron_variant - - - - - - rs4650045 1:70859425 T - - - intergenic_variant - - - - - - rs1022530 1:71490287 C CCDS44160.1 CCDS44160.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C CCDS658.1 CCDS658.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C 5733 NM_198719.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C 5733 NM_198716.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C 5733 NR_028294.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1022530 1:71490287 C 5733 NM_001126044.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C CCDS656.1 CCDS656.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C 5733 NM_198718.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C ENSESTG00000030999 ENSESTT00000078021 Transcript intron_variant - - - - - - rs1022530 1:71490287 C 5733 NM_198715.2 Transcript intron_variant - - - - - - rs1022530 1:71490287 C 5733 NR_028293.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1022530 1:71490287 C CCDS655.1 CCDS655.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C 5733 NR_028292.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1022530 1:71490287 C 5733 NM_198714.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C CCDS657.1 CCDS657.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C 5733 NM_198717.1 Transcript intron_variant - - - - - - rs1022530 1:71490287 C CCDS652.1 CCDS652.1 Transcript intron_variant - - - - - - rs782215 1:72944650 A - - - intergenic_variant - - - - - - rs4551547 1:73063963 C - - - intergenic_variant - - - - - - rs6704327 1:73586067 C - - - intergenic_variant - - - - - - rs1923215 1:73828976 A - - - intergenic_variant - - - - - - rs1501487 1:73995815 A - - - intergenic_variant - - - - - - rs6703287 1:74003908 C - - - intergenic_variant - - - - - - rs2133826 1:74011344 C - - - intergenic_variant - - - - - - rs1121416 1:74046105 C - - - intergenic_variant - - - - - - rs1604351 1:74080088 T - - - intergenic_variant - - - - - - rs4282754 1:74160918 A - - - intergenic_variant - - - - - - rs6701335 1:74234235 T - - - intergenic_variant - - - - - - rs7545112 1:74340667 G - - - intergenic_variant - - - - - - rs1384881 1:74498569 A 127255 NM_001105659.1 Transcript intron_variant - - - - - - rs1384881 1:74498569 A ENSESTG00000010461 ENSESTT00000026209 Transcript intron_variant - - - - - - rs1384881 1:74498569 A CCDS41350.1 CCDS41350.1 Transcript intron_variant - - - - - - rs1384881 1:74498569 A ENSESTG00000010461 ENSESTT00000026202 Transcript intron_variant - - - - - - rs1384881 1:74498569 A ENSESTG00000010461 ENSESTT00000026196 Transcript intron_variant - - - - - - rs1022263 1:74979467 A CCDS664.1 CCDS664.1 Transcript intron_variant - - - - - - rs1022263 1:74979467 A ENSESTG00000032454 ENSESTT00000081940 Transcript intron_variant - - - - - - rs1022263 1:74979467 A CCDS44161.1 CCDS44161.1 Transcript intron_variant - - - - - - rs1022263 1:74979467 A 100526835 NM_001112808.2 Transcript intron_variant - - - - - - rs1022263 1:74979467 A 51086 NM_015978.2 Transcript intron_variant - - - - - - rs277349 1:75309345 G - - - intergenic_variant - - - - - - rs146861659 1:75384151 T - - - intergenic_variant - - - - - - rs795570 1:75539388 T - - - intergenic_variant - - - - - - rs374872 1:75555775 A - - - intergenic_variant - - - - - - rs373427 1:75589126 A 431707 NM_001001933.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4993 rs1526501 1:75606177 G CCDS30756.1 CCDS30756.1 Transcript intron_variant - - - - - - rs1526501 1:75606177 G ENSESTG00000032522 ENSESTT00000082144 Transcript intron_variant - - - - - - rs1526501 1:75606177 G CCDS58008.1 CCDS58008.1 Transcript intron_variant - - - - - - rs1526501 1:75606177 G 431707 NM_001001933.1 Transcript intron_variant - - - - - - rs1526501 1:75606177 G ENSESTG00000032522 ENSESTT00000082134 Transcript intron_variant - - - - - - rs1526501 1:75606177 G 431707 NM_001256114.1 Transcript intron_variant - - - - - - rs2222678 1:75617932 C CCDS30756.1 CCDS30756.1 Transcript intron_variant - - - - - - rs2222678 1:75617932 C ENSESTG00000032522 ENSESTT00000082144 Transcript intron_variant - - - - - - rs2222678 1:75617932 C CCDS58008.1 CCDS58008.1 Transcript intron_variant - - - - - - rs2222678 1:75617932 C 431707 NM_001001933.1 Transcript intron_variant - - - - - - rs2222678 1:75617932 C ENSESTG00000032522 ENSESTT00000082134 Transcript intron_variant - - - - - - rs2222678 1:75617932 C 431707 NM_001256114.1 Transcript intron_variant - - - - - - rs7540448 1:75631966 T 431707 NM_001001933.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4748 rs7540448 1:75631966 T 431707 NM_001256114.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4748 rs1852343 1:75647635 T - - - intergenic_variant - - - - - - rs941033 1:75659289 G - - - intergenic_variant - - - - - - rs1358164 1:75662267 G - - - intergenic_variant - - - - - - rs588478 1:75701437 C CCDS667.1 CCDS667.1 Transcript intron_variant - - - - - - rs588478 1:75701437 C 204962 NM_001130058.1 Transcript intron_variant - - - - - - rs588478 1:75701437 C ENSESTG00000032552 ENSESTT00000082223 Transcript intron_variant - - - - - - rs588478 1:75701437 C ENSESTG00000032552 ENSESTT00000082237 Transcript intron_variant - - - - - - rs588478 1:75701437 C 204962 NM_152697.4 Transcript intron_variant - - - - - - rs588478 1:75701437 C CCDS44164.1 CCDS44164.1 Transcript intron_variant - - - - - - rs1249836 1:75820083 T - ENSR00000670312 RegulatoryFeature regulatory_region_variant - - - - - - rs1249836 1:75820083 T ENSESTG00000032552 ENSESTT00000082231 Transcript intron_variant - - - - - - rs1249836 1:75820083 T ENSESTG00000032552 ENSESTT00000082223 Transcript intron_variant - - - - - - rs1249836 1:75820083 T 204962 NM_152697.4 Transcript intron_variant - - - - - - rs1249836 1:75820083 T CCDS667.1 CCDS667.1 Transcript intron_variant - - - - - - rs1249836 1:75820083 T 204962 NM_001130058.1 Transcript intron_variant - - - - - - rs1249836 1:75820083 T ENSESTG00000011806 ENSESTT00000029625 Transcript intron_variant - - - - - - rs1249836 1:75820083 T CCDS44164.1 CCDS44164.1 Transcript intron_variant - - - - - - rs1249836 1:75820083 T ENSESTG00000011806 ENSESTT00000029619 Transcript intron_variant - - - - - - rs1249806 1:75840212 G ENSESTG00000032552 ENSESTT00000082231 Transcript intron_variant - - - - - - rs1249806 1:75840212 G ENSESTG00000032552 ENSESTT00000082223 Transcript intron_variant - - - - - - rs1249806 1:75840212 G 204962 NM_152697.4 Transcript intron_variant - - - - - - rs1249806 1:75840212 G CCDS667.1 CCDS667.1 Transcript intron_variant - - - - - - rs1249806 1:75840212 G 204962 NM_001130058.1 Transcript intron_variant - - - - - - rs1249806 1:75840212 G ENSESTG00000011806 ENSESTT00000029625 Transcript intron_variant - - - - - - rs1249806 1:75840212 G CCDS44164.1 CCDS44164.1 Transcript intron_variant - - - - - - rs1249806 1:75840212 G ENSESTG00000011806 ENSESTT00000029619 Transcript intron_variant - - - - - - rs1249798 1:75878111 C ENSESTG00000032552 ENSESTT00000082231 Transcript intron_variant - - - - - - rs1249798 1:75878111 C ENSESTG00000032552 ENSESTT00000082223 Transcript intron_variant - - - - - - rs1249798 1:75878111 C 204962 NM_152697.4 Transcript intron_variant - - - - - - rs1249798 1:75878111 C CCDS667.1 CCDS667.1 Transcript intron_variant - - - - - - rs1249798 1:75878111 C 204962 NM_001130058.1 Transcript intron_variant - - - - - - rs1249798 1:75878111 C ENSESTG00000011806 ENSESTT00000029625 Transcript intron_variant - - - - - - rs1249798 1:75878111 C CCDS44164.1 CCDS44164.1 Transcript intron_variant - - - - - - rs1249798 1:75878111 C ENSESTG00000011806 ENSESTT00000029619 Transcript intron_variant - - - - - - rs1249802 1:75881066 C ENSESTG00000032552 ENSESTT00000082231 Transcript intron_variant - - - - - - rs1249802 1:75881066 C ENSESTG00000032552 ENSESTT00000082223 Transcript intron_variant - - - - - - rs1249802 1:75881066 C 204962 NM_152697.4 Transcript intron_variant - - - - - - rs1249802 1:75881066 C CCDS667.1 CCDS667.1 Transcript intron_variant - - - - - - rs1249802 1:75881066 C 204962 NM_001130058.1 Transcript intron_variant - - - - - - rs1249802 1:75881066 C ENSESTG00000011806 ENSESTT00000029625 Transcript intron_variant - - - - - - rs1249802 1:75881066 C CCDS44164.1 CCDS44164.1 Transcript intron_variant - - - - - - rs1249802 1:75881066 C ENSESTG00000011806 ENSESTT00000029619 Transcript intron_variant - - - - - - rs2799053 1:75961515 T ENSESTG00000032552 ENSESTT00000082231 Transcript intron_variant - - - - - - rs2799053 1:75961515 T ENSESTG00000032552 ENSESTT00000082223 Transcript intron_variant - - - - - - rs2799053 1:75961515 T 204962 NM_152697.4 Transcript intron_variant - - - - - - rs2799053 1:75961515 T CCDS667.1 CCDS667.1 Transcript intron_variant - - - - - - rs2799053 1:75961515 T 204962 NM_001130058.1 Transcript intron_variant - - - - - - rs2799053 1:75961515 T ENSESTG00000011806 ENSESTT00000029625 Transcript intron_variant - - - - - - rs2799053 1:75961515 T CCDS44164.1 CCDS44164.1 Transcript intron_variant - - - - - - rs2799053 1:75961515 T ENSESTG00000011806 ENSESTT00000029619 Transcript intron_variant - - - - - - rs1475679 1:75983509 C ENSESTG00000032552 ENSESTT00000082231 Transcript intron_variant - - - - - - rs1475679 1:75983509 C ENSESTG00000032552 ENSESTT00000082223 Transcript intron_variant - - - - - - rs1475679 1:75983509 C 204962 NM_152697.4 Transcript intron_variant - - - - - - rs1475679 1:75983509 C CCDS667.1 CCDS667.1 Transcript intron_variant - - - - - - rs1475679 1:75983509 C 204962 NM_001130058.1 Transcript intron_variant - - - - - - rs1475679 1:75983509 C ENSESTG00000011806 ENSESTT00000029625 Transcript intron_variant - - - - - - rs1475679 1:75983509 C CCDS44164.1 CCDS44164.1 Transcript intron_variant - - - - - - rs1475679 1:75983509 C ENSESTG00000011806 ENSESTT00000029619 Transcript intron_variant - - - - - - rs2587038 1:75984462 T ENSESTG00000032552 ENSESTT00000082231 Transcript intron_variant - - - - - - rs2587038 1:75984462 T ENSESTG00000032552 ENSESTT00000082223 Transcript intron_variant - - - - - - rs2587038 1:75984462 T 204962 NM_152697.4 Transcript intron_variant - - - - - - rs2587038 1:75984462 T CCDS667.1 CCDS667.1 Transcript intron_variant - - - - - - rs2587038 1:75984462 T 204962 NM_001130058.1 Transcript intron_variant - - - - - - rs2587038 1:75984462 T ENSESTG00000011806 ENSESTT00000029625 Transcript intron_variant - - - - - - rs2587038 1:75984462 T CCDS44164.1 CCDS44164.1 Transcript intron_variant - - - - - - rs2587038 1:75984462 T ENSESTG00000011806 ENSESTT00000029619 Transcript intron_variant - - - - - - rs6593536 1:76891290 G - ENSR00000539200 RegulatoryFeature regulatory_region_variant - - - - - - rs6593536 1:76891290 G ENSESTG00000031502 ENSESTT00000079455 Transcript intron_variant - - - - - - rs6593536 1:76891290 G 256435 NM_001160011.1 Transcript intron_variant - - - - - - rs6593536 1:76891290 G 256435 NM_152996.2 Transcript intron_variant - - - - - - rs6593536 1:76891290 G CCDS672.1 CCDS672.1 Transcript intron_variant - - - - - - rs10747348 1:76992184 T ENSESTG00000031502 ENSESTT00000079455 Transcript intron_variant - - - - - - rs10747348 1:76992184 T 256435 NM_001160011.1 Transcript intron_variant - - - - - - rs10747348 1:76992184 T 256435 NM_152996.2 Transcript intron_variant - - - - - - rs10747348 1:76992184 T CCDS672.1 CCDS672.1 Transcript intron_variant - - - - - - rs962669 1:77217069 G - - - intergenic_variant - - - - - - rs2647393 1:77226795 G - - - intergenic_variant - - - - - - rs7543646 1:77567040 C ENSESTG00000031616 ENSESTT00000079826 Transcript intron_variant - - - - - - rs7543646 1:77567040 C ENSESTG00000031616 ENSESTT00000079816 Transcript intron_variant - - - - - - rs7543646 1:77567040 C CCDS674.1 CCDS674.1 Transcript intron_variant - - - - - - rs7543646 1:77567040 C ENSESTG00000031616 ENSESTT00000079771 Transcript intron_variant - - - - - - rs7543646 1:77567040 C 10026 NM_005482.2 Transcript intron_variant - - - - - - rs2799566 1:77686411 T - ENSR00001521720 RegulatoryFeature regulatory_region_variant - - - - - - rs2799566 1:77686411 T ENSESTG00000031616 ENSESTT00000079826 Transcript upstream_gene_variant - - - - - - DISTANCE=1320 rs2799566 1:77686411 T ENSESTG00000031616 ENSESTT00000079816 Transcript upstream_gene_variant - - - - - - DISTANCE=1298 rs2799566 1:77686411 T CCDS674.1 CCDS674.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1324 rs2799566 1:77686411 T ENSESTG00000031616 ENSESTT00000079771 Transcript upstream_gene_variant - - - - - - DISTANCE=1296 rs2799566 1:77686411 T 10026 NM_005482.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1279 rs7410814 1:78314263 A ENSESTG00000002465 ENSESTT00000006148 Transcript intron_variant - - - - - - rs7410814 1:78314263 A CCDS681.1 CCDS681.1 Transcript intron_variant - - - - - - rs7410814 1:78314263 A 374986 NM_198549.3 Transcript intron_variant - - - - - - rs7410814 1:78314263 A ENSESTG00000002465 ENSESTT00000006140 Transcript intron_variant - - - - - - rs7410814 1:78314263 A ENSESTG00000002465 ENSESTT00000006147 Transcript intron_variant - - - - - - rs7410814 1:78314263 A 374986 NM_001270384.1 Transcript intron_variant - - - - - - rs1322925 1:78914446 C - - - intergenic_variant - - - - - - rs1780772 1:79331127 A - - - intergenic_variant - - - - - - rs1494860 1:80021493 G - - - intergenic_variant - - - - - - rs4650466 1:80941828 T ENSESTG00000019438 ENSESTT00000048810 Transcript intron_variant - - - - - - rs1886145 1:81238232 G - - - intergenic_variant - - - - - - rs538125 1:82129697 C - - - intergenic_variant - - - - - - rs6598973 1:82417201 C ENSESTG00000024287 ENSESTT00000061684 Transcript intron_variant - - - - - - rs6598973 1:82417201 C ENSESTG00000024287 ENSESTT00000061715 Transcript intron_variant - - - - - - rs6598973 1:82417201 C 23266 NM_012302.2 Transcript intron_variant - - - - - - rs6598973 1:82417201 C ENSESTG00000024287 ENSESTT00000061746 Transcript intron_variant - - - - - - rs6598973 1:82417201 C ENSESTG00000024287 ENSESTT00000061759 Transcript downstream_gene_variant - - - - - - DISTANCE=1034 rs6598973 1:82417201 C ENSESTG00000024451 ENSESTT00000061823 Transcript intron_variant - - - - - - rs6598973 1:82417201 C ENSESTG00000024287 ENSESTT00000061733 Transcript intron_variant - - - - - - rs6598973 1:82417201 C CCDS689.1 CCDS689.1 Transcript intron_variant - - - - - - rs1281601 1:82885739 C - - - intergenic_variant - - - - - - rs1292785 1:82925828 A - - - intergenic_variant - - - - - - rs631645 1:84356502 A ENSESTG00000030559 ENSESTT00000076994 Transcript intron_variant - - - - - - rs631645 1:84356502 A ENSESTG00000030559 ENSESTT00000076988 Transcript intron_variant - - - - - - rs631645 1:84356502 A CCDS690.2 CCDS690.2 Transcript intron_variant - - - - - - rs631645 1:84356502 A 79739 NM_024686.4 Transcript intron_variant - - - - - - rs597653 1:84361635 G ENSESTG00000030559 ENSESTT00000076994 Transcript intron_variant - - - - - - rs597653 1:84361635 G ENSESTG00000030559 ENSESTT00000076988 Transcript intron_variant - - - - - - rs597653 1:84361635 G CCDS690.2 CCDS690.2 Transcript intron_variant - - - - - - rs597653 1:84361635 G 79739 NM_024686.4 Transcript intron_variant - - - - - - rs1748184 1:84371389 G ENSESTG00000030559 ENSESTT00000076994 Transcript intron_variant - - - - - - rs1748184 1:84371389 G ENSESTG00000030559 ENSESTT00000076988 Transcript intron_variant - - - - - - rs1748184 1:84371389 G CCDS690.2 CCDS690.2 Transcript intron_variant - - - - - - rs1748184 1:84371389 G 79739 NM_024686.4 Transcript intron_variant - - - - - - rs567127 1:84427199 C ENSESTG00000030488 ENSESTT00000076764 Transcript intron_variant - - - - - - rs567127 1:84427199 C ENSESTG00000030488 ENSESTT00000076804 Transcript intron_variant - - - - - - rs567127 1:84427199 C 79739 NM_024686.4 Transcript intron_variant - - - - - - rs567127 1:84427199 C ENSESTG00000030488 ENSESTT00000076815 Transcript intron_variant - - - - - - rs6675854 1:84442237 A ENSESTG00000030488 ENSESTT00000076764 Transcript intron_variant - - - - - - rs6675854 1:84442237 A ENSESTG00000030488 ENSESTT00000076804 Transcript intron_variant - - - - - - rs6675854 1:84442237 A 79739 NM_024686.4 Transcript intron_variant - - - - - - rs6675854 1:84442237 A ENSESTG00000030488 ENSESTT00000076815 Transcript intron_variant - - - - - - rs627712 1:84501140 C - - - intergenic_variant - - - - - - rs2812000 1:84626101 A CCDS691.1 CCDS691.1 Transcript intron_variant - - - - - - rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076279 Transcript upstream_gene_variant - - - - - - DISTANCE=4247 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076149 Transcript upstream_gene_variant - - - - - - DISTANCE=3831 rs2812000 1:84626101 A CCDS692.1 CCDS692.1 Transcript intron_variant - - - - - - rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076147 Transcript upstream_gene_variant - - - - - - DISTANCE=3831 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076202 Transcript upstream_gene_variant - - - - - - DISTANCE=3917 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076230 Transcript upstream_gene_variant - - - - - - DISTANCE=4060 rs2812000 1:84626101 A 5567 NM_001242858.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3964 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076109 Transcript intron_variant - - - - - - rs2812000 1:84626101 A CCDS55610.1 CCDS55610.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3995 rs2812000 1:84626101 A 5567 NM_002731.2 Transcript intron_variant - - - - - - rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076072 Transcript intron_variant - - - - - - rs2812000 1:84626101 A CCDS55609.1 CCDS55609.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3995 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076228 Transcript upstream_gene_variant - - - - - - DISTANCE=4060 rs2812000 1:84626101 A 5567 NM_207578.1 Transcript intron_variant - - - - - - rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076095 Transcript intron_variant - - - - - - rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076168 Transcript upstream_gene_variant - - - - - - DISTANCE=3889 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076291 Transcript upstream_gene_variant - - - - - - DISTANCE=4247 rs2812000 1:84626101 A CCDS693.1 CCDS693.1 Transcript intron_variant - - - - - - rs2812000 1:84626101 A 5567 NM_001242861.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4548 rs2812000 1:84626101 A 5567 NM_182948.2 Transcript intron_variant - - - - - - rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076306 Transcript upstream_gene_variant - - - - - - DISTANCE=4279 rs2812000 1:84626101 A 5567 NM_001242857.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3964 rs2812000 1:84626101 A 5567 NM_001242859.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3964 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076052 Transcript intron_variant - - - - - - rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076176 Transcript upstream_gene_variant - - - - - - DISTANCE=3889 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076107 Transcript intron_variant - - - - - - rs2812000 1:84626101 A 5567 NM_001242860.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4548 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076233 Transcript upstream_gene_variant - - - - - - DISTANCE=4060 rs2812000 1:84626101 A CCDS55611.1 CCDS55611.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4589 rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076008 Transcript intron_variant - - - - - - rs2812000 1:84626101 A ENSESTG00000030137 ENSESTT00000076213 Transcript upstream_gene_variant - - - - - - DISTANCE=3917 rs2792465 1:84772723 T 148418 NM_001134663.1 Transcript intron_variant - - - - - - rs2792465 1:84772723 T CCDS30760.1 CCDS30760.1 Transcript intron_variant - - - - - - rs2792465 1:84772723 T 148418 NM_001010971.2 Transcript intron_variant - - - - - - rs2792465 1:84772723 T ENSESTG00000002235 ENSESTT00000005598 Transcript downstream_gene_variant - - - - - - DISTANCE=3416 rs2792465 1:84772723 T ENSESTG00000002235 ENSESTT00000005600 Transcript intron_variant - - - - - - rs2792465 1:84772723 T ENSESTG00000002235 ENSESTT00000005608 Transcript intron_variant - - - - - - rs2792465 1:84772723 T 148418 NM_001134664.1 Transcript intron_variant - - - - - - rs2792465 1:84772723 T ENSESTG00000002235 ENSESTT00000005602 Transcript intron_variant - - - - - - rs2792465 1:84772723 T CCDS44166.1 CCDS44166.1 Transcript intron_variant - - - - - - rs511063 1:84824499 C ENSESTG00000002235 ENSESTT00000005616 Transcript intron_variant - - - - - - rs2792464 1:84827007 T ENSESTG00000002235 ENSESTT00000005616 Transcript intron_variant - - - - - - rs2792464 1:84827007 T 391051 NR_003927.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3634 rs7531176 1:84901772 A - - - intergenic_variant - - - - - - rs4581293 1:84927620 T - - - intergenic_variant - - - - - - rs6576709 1:84931639 A - - - intergenic_variant - - - - - - rs818519 1:85210622 A - - - intergenic_variant - - - - - - rs233116 1:85787114 T 23576 NM_001134445.1 Transcript 3_prime_UTR_variant 1072 - - - - - rs233116 1:85787114 T 23576 NM_012137.3 Transcript 3_prime_UTR_variant 1040 - - - - - rs233116 1:85787114 T ENSESTG00000001201 ENSESTT00000002917 Transcript downstream_gene_variant - - - - - - DISTANCE=50 rs233116 1:85787114 T ENSESTG00000001176 ENSESTT00000002807 Transcript intron_variant - - - - - - rs233116 1:85787114 T CCDS44170.1 CCDS44170.1 Transcript downstream_gene_variant - - - - - - DISTANCE=21 rs233116 1:85787114 T ENSESTG00000001201 ENSESTT00000002897 Transcript downstream_gene_variant - - - - - - DISTANCE=80 rs233116 1:85787114 T CCDS705.1 CCDS705.1 Transcript downstream_gene_variant - - - - - - DISTANCE=21 rs233116 1:85787114 T ENSESTG00000001201 ENSESTT00000002912 Transcript downstream_gene_variant - - - - - - DISTANCE=26 rs263434 1:87177033 A CCDS55612.1 CCDS55612.1 Transcript intron_variant - - - - - - rs263434 1:87177033 A ENSESTG00000026852 ENSESTT00000067808 Transcript intron_variant - - - - - - rs263434 1:87177033 A 51100 NM_016009.4 Transcript intron_variant - - - - - - rs263434 1:87177033 A ENSESTG00000026852 ENSESTT00000067825 Transcript intron_variant - - - - - - rs263434 1:87177033 A 51100 NM_001206653.1 Transcript intron_variant - - - - - - rs263434 1:87177033 A 51100 NM_001206652.1 Transcript intron_variant - - - - - - rs263434 1:87177033 A CCDS710.1 CCDS710.1 Transcript intron_variant - - - - - - rs263434 1:87177033 A 51100 NM_001206651.1 Transcript intron_variant - - - - - - rs174500 1:87241944 T - - - intergenic_variant - - - - - - rs11161979 1:87780315 C - - - intergenic_variant - - - - - - rs2491314 1:88335945 A - - - intergenic_variant - - - - - - rs12038850 1:88771977 T - - - intergenic_variant - - - - - - rs4363406 1:89679728 A ENSESTG00000024669 ENSESTT00000062447 Transcript intron_variant - - - - - - rs4363406 1:89679728 A ENSESTG00000024669 ENSESTT00000062355 Transcript intron_variant - - - - - - rs673933 1:89745422 C - - - intergenic_variant - - - - - - rs6428522 1:89820128 A - - - intergenic_variant - - - - - - rs10735787 1:92048082 C - ENSR00001522385 RegulatoryFeature regulatory_region_variant - - - - - - rs10735787 1:92048082 C - - - intergenic_variant - - - - - - rs1192407 1:92069689 G - - - intergenic_variant - - - - - - rs569211 1:92605350 T CCDS737.1 CCDS737.1 Transcript intron_variant - - - - - - rs569211 1:92605350 T 284697 NM_183242.3 Transcript intron_variant - - - - - - rs3118136 1:92653687 A 23285 NM_015237.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3407 rs3118136 1:92653687 A CCDS44172.1 CCDS44172.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3800 rs2992963 1:93552788 A CCDS53340.1 CCDS53340.1 Transcript intron_variant - - - - - - rs2992963 1:93552788 A ENSESTG00000020561 ENSESTT00000051881 Transcript intron_variant - - - - - - rs2992963 1:93552788 A ENSESTG00000020561 ENSESTT00000051954 Transcript intron_variant - - - - - - rs2992963 1:93552788 A CCDS742.1 CCDS742.1 Transcript intron_variant - - - - - - rs2992963 1:93552788 A 22823 NM_007358.3 Transcript intron_variant - - - - - - rs2992963 1:93552788 A 22823 NM_001164392.1 Transcript intron_variant - - - - - - rs2992963 1:93552788 A 22823 NM_001164393.1 Transcript intron_variant - - - - - - rs2992963 1:93552788 A ENSESTG00000020561 ENSESTT00000051856 Transcript intron_variant - - - - - - rs2992963 1:93552788 A ENSESTG00000020561 ENSESTT00000051931 Transcript intron_variant - - - - - - rs2992963 1:93552788 A 22823 NM_001164391.1 Transcript intron_variant - - - - - - rs2992963 1:93552788 A ENSESTG00000020561 ENSESTT00000051919 Transcript intron_variant - - - - - - rs2749733 1:93564386 A CCDS53340.1 CCDS53340.1 Transcript intron_variant - - - - - - rs2749733 1:93564386 A ENSESTG00000020561 ENSESTT00000051881 Transcript intron_variant - - - - - - rs2749733 1:93564386 A ENSESTG00000020561 ENSESTT00000051954 Transcript intron_variant - - - - - - rs2749733 1:93564386 A CCDS742.1 CCDS742.1 Transcript intron_variant - - - - - - rs2749733 1:93564386 A 22823 NM_007358.3 Transcript intron_variant - - - - - - rs2749733 1:93564386 A 22823 NM_001164392.1 Transcript intron_variant - - - - - - rs2749733 1:93564386 A 22823 NM_001164393.1 Transcript intron_variant - - - - - - rs2749733 1:93564386 A ENSESTG00000020561 ENSESTT00000051856 Transcript intron_variant - - - - - - rs2749733 1:93564386 A ENSESTG00000020561 ENSESTT00000051931 Transcript intron_variant - - - - - - rs2749733 1:93564386 A 22823 NM_001164391.1 Transcript intron_variant - - - - - - rs2749733 1:93564386 A ENSESTG00000020561 ENSESTT00000051919 Transcript intron_variant - - - - - - rs2749729 1:93591046 A CCDS53340.1 CCDS53340.1 Transcript intron_variant - - - - - - rs2749729 1:93591046 A ENSESTG00000020561 ENSESTT00000051881 Transcript intron_variant - - - - - - rs2749729 1:93591046 A CCDS742.1 CCDS742.1 Transcript intron_variant - - - - - - rs2749729 1:93591046 A ENSESTG00000020561 ENSESTT00000051966 Transcript upstream_gene_variant - - - - - - DISTANCE=1716 rs2749729 1:93591046 A 22823 NM_007358.3 Transcript intron_variant - - - - - - rs2749729 1:93591046 A 22823 NM_001164392.1 Transcript intron_variant - - - - - - rs2749729 1:93591046 A 22823 NM_001164393.1 Transcript intron_variant - - - - - - rs2749729 1:93591046 A ENSESTG00000020561 ENSESTT00000051856 Transcript intron_variant - - - - - - rs2749729 1:93591046 A ENSESTG00000020561 ENSESTT00000051931 Transcript intron_variant - - - - - - rs2749729 1:93591046 A CCDS53341.1 CCDS53341.1 Transcript intron_variant - - - - - - rs2749729 1:93591046 A 22823 NM_001164391.1 Transcript intron_variant - - - - - - rs1537756 1:93623157 T CCDS53342.1 CCDS53342.1 Transcript intron_variant - - - - - - rs1537756 1:93623157 T CCDS743.1 CCDS743.1 Transcript intron_variant - - - - - - rs1537756 1:93623157 T ENSESTG00000020836 ENSESTT00000052281 Transcript intron_variant - - - - - - rs1537756 1:93623157 T 50999 NR_030761.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1537756 1:93623157 T 50999 NM_001167830.1 Transcript intron_variant - - - - - - rs1537756 1:93623157 T 50999 NM_016040.4 Transcript intron_variant - - - - - - rs4459120 1:93957412 T CCDS53344.1 CCDS53344.1 Transcript intron_variant - - - - - - rs4459120 1:93957412 T 54874 NM_001164473.2 Transcript intron_variant - - - - - - rs4459120 1:93957412 T CCDS53343.1 CCDS53343.1 Transcript intron_variant - - - - - - rs4459120 1:93957412 T 54874 NM_017737.4 Transcript intron_variant - - - - - - rs4459120 1:93957412 T 54874 NM_001024948.2 Transcript intron_variant - - - - - - rs841700 1:95047648 C - - - intergenic_variant - - - - - - rs698955 1:95336947 T - ENSR00001522650 RegulatoryFeature regulatory_region_variant - - - - - - rs698955 1:95336947 T ENSESTG00000027572 ENSESTT00000069614 Transcript intron_variant - - - - - - rs698955 1:95336947 T ENSESTG00000027572 ENSESTT00000069632 Transcript intron_variant - - - - - - rs698955 1:95336947 T 126969 NM_001258343.1 Transcript intron_variant - - - - - - rs698955 1:95336947 T 126969 NM_001258340.1 Transcript intron_variant - - - - - - rs698955 1:95336947 T CCDS58013.1 CCDS58013.1 Transcript intron_variant - - - - - - rs698955 1:95336947 T CCDS44176.1 CCDS44176.1 Transcript intron_variant - - - - - - rs698955 1:95336947 T CCDS58012.1 CCDS58012.1 Transcript intron_variant - - - - - - rs698955 1:95336947 T 126969 NM_152369.4 Transcript intron_variant - - - - - - rs698955 1:95336947 T 126969 NM_001114106.2 Transcript intron_variant - - - - - - rs698955 1:95336947 T 126969 NM_001258342.1 Transcript intron_variant - - - - - - rs698955 1:95336947 T CCDS58011.1 CCDS58011.1 Transcript intron_variant - - - - - - rs698955 1:95336947 T CCDS751.1 CCDS751.1 Transcript intron_variant - - - - - - rs698955 1:95336947 T 126969 NM_001258341.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C ENSESTG00000027572 ENSESTT00000069614 Transcript intron_variant - - - - - - rs698968 1:95353022 C ENSESTG00000027572 ENSESTT00000069632 Transcript intron_variant - - - - - - rs698968 1:95353022 C 126969 NM_001258343.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C 126969 NM_001258340.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C CCDS58013.1 CCDS58013.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C CCDS44176.1 CCDS44176.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C CCDS58012.1 CCDS58012.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C 126969 NM_152369.4 Transcript intron_variant - - - - - - rs698968 1:95353022 C 126969 NM_001114106.2 Transcript intron_variant - - - - - - rs698968 1:95353022 C 126969 NM_001258342.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C CCDS58011.1 CCDS58011.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C CCDS751.1 CCDS751.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C 126969 NM_001258341.1 Transcript intron_variant - - - - - - rs698968 1:95353022 C ENSESTG00000027873 ENSESTT00000070150 Transcript upstream_gene_variant - - - - - - DISTANCE=4917 rs2391673 1:95921472 C - - - intergenic_variant - - - - - - rs1146528 1:96488283 C ENSESTG00000006753 ENSESTT00000017133 Transcript missense_variant 299 140 47 V/A gTt/gCt - rs1146528 1:96488283 C ENSESTG00000006753 ENSESTT00000017127 Transcript missense_variant 275 140 47 V/A gTt/gCt - rs326650 1:96774287 A - - - intergenic_variant - - - - - - rs226974 1:96782917 T - - - intergenic_variant - - - - - - rs80014790 1:96935679 A - - - intergenic_variant - - - - - - rs2088094 1:97335216 G - - - intergenic_variant - - - - - - rs2681191 1:97342002 G - - - intergenic_variant - - - - - - rs2932316 1:97393608 G - - - intergenic_variant - - - - - - rs2946751 1:97393702 A - - - intergenic_variant - - - - - - rs3002270 1:97444640 C - - - intergenic_variant - - - - - - rs290832 1:97455412 A - - - intergenic_variant - - - - - - rs290834 1:97459068 A - - - intergenic_variant - - - - - - rs290814 1:97490758 A - - - intergenic_variant - - - - - - rs290836 1:97510326 A - - - intergenic_variant - - - - - - rs290856 1:97527122 C - - - intergenic_variant - - - - - - rs290866 1:97540303 A 1806 NM_000110.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2996 rs290866 1:97540303 A CCDS30777.1 CCDS30777.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4229 rs290866 1:97540303 A ENSESTG00000012998 ENSESTT00000032608 Transcript downstream_gene_variant - - - - - - DISTANCE=3821 rs290854 1:97547831 A - ENSR00001522782 RegulatoryFeature regulatory_region_variant - - - - - - rs290854 1:97547831 A 1806 NM_000110.3 Transcript intron_variant - - - - - - rs290854 1:97547831 A CCDS30777.1 CCDS30777.1 Transcript intron_variant - - - - - - rs290854 1:97547831 A ENSESTG00000012998 ENSESTT00000032608 Transcript intron_variant - - - - - - rs993569 1:97571834 G 100873932 NR_046590.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs993569 1:97571834 G 1806 NM_000110.3 Transcript intron_variant - - - - - - rs993569 1:97571834 G CCDS30777.1 CCDS30777.1 Transcript intron_variant - - - - - - rs993569 1:97571834 G ENSESTG00000012998 ENSESTT00000032608 Transcript intron_variant - - - - - - rs28371444 1:97794364 T ENSESTG00000008005 ENSESTT00000020235 Transcript 5_prime_UTR_variant 1029 - - - - - rs28371444 1:97794364 T 1806 NM_000110.3 Transcript intron_variant - - - - - - rs28371444 1:97794364 T ENSESTG00000008056 ENSESTT00000020364 Transcript intron_variant - - - - - - rs28371444 1:97794364 T CCDS30777.1 CCDS30777.1 Transcript intron_variant - - - - - - rs28371444 1:97794364 T ENSESTG00000012998 ENSESTT00000032608 Transcript intron_variant - - - - - - rs11165909 1:98248418 C ENSESTG00000008032 ENSESTT00000020336 Transcript intron_variant - - - - - - rs11165909 1:98248418 C ENSESTG00000008032 ENSESTT00000020357 Transcript intron_variant - - - - - - rs11165909 1:98248418 C ENSESTG00000008032 ENSESTT00000020349 Transcript intron_variant - - - - - - rs11165909 1:98248418 C 1806 NM_000110.3 Transcript intron_variant - - - - - - rs11165909 1:98248418 C CCDS30777.1 CCDS30777.1 Transcript intron_variant - - - - - - rs11165909 1:98248418 C 1806 NM_001160301.1 Transcript intron_variant - - - - - - rs11165909 1:98248418 C CCDS53346.1 CCDS53346.1 Transcript intron_variant - - - - - - rs6604118 1:98323962 T ENSESTG00000008032 ENSESTT00000020336 Transcript intron_variant - - - - - - rs6604118 1:98323962 T ENSESTG00000008032 ENSESTT00000020357 Transcript intron_variant - - - - - - rs6604118 1:98323962 T ENSESTG00000008032 ENSESTT00000020349 Transcript intron_variant - - - - - - rs6604118 1:98323962 T 1806 NM_000110.3 Transcript intron_variant - - - - - - rs6604118 1:98323962 T CCDS30777.1 CCDS30777.1 Transcript intron_variant - - - - - - rs6604118 1:98323962 T 1806 NM_001160301.1 Transcript intron_variant - - - - - - rs6604118 1:98323962 T CCDS53346.1 CCDS53346.1 Transcript intron_variant - - - - - - rs4411156 1:98347940 A ENSESTG00000008032 ENSESTT00000020336 Transcript intron_variant - - - - - - rs4411156 1:98347940 A ENSESTG00000008032 ENSESTT00000020357 Transcript intron_variant - - - - - - rs4411156 1:98347940 A ENSESTG00000008032 ENSESTT00000020349 Transcript intron_variant - - - - - - rs4411156 1:98347940 A 1806 NM_000110.3 Transcript intron_variant - - - - - - rs4411156 1:98347940 A CCDS30777.1 CCDS30777.1 Transcript intron_variant - - - - - - rs4411156 1:98347940 A 1806 NM_001160301.1 Transcript intron_variant - - - - - - rs4411156 1:98347940 A CCDS53346.1 CCDS53346.1 Transcript intron_variant - - - - - - rs4579796 1:98372913 T - ENSR00000541520 RegulatoryFeature regulatory_region_variant - - - - - - rs4579796 1:98372913 T ENSESTG00000008032 ENSESTT00000020336 Transcript intron_variant - - - - - - rs4579796 1:98372913 T ENSESTG00000008032 ENSESTT00000020357 Transcript intron_variant - - - - - - rs4579796 1:98372913 T ENSESTG00000008032 ENSESTT00000020349 Transcript intron_variant - - - - - - rs4579796 1:98372913 T 1806 NM_000110.3 Transcript intron_variant - - - - - - rs4579796 1:98372913 T CCDS30777.1 CCDS30777.1 Transcript intron_variant - - - - - - rs4579796 1:98372913 T 1806 NM_001160301.1 Transcript intron_variant - - - - - - rs4579796 1:98372913 T CCDS53346.1 CCDS53346.1 Transcript intron_variant - - - - - - rs4266922 1:98385251 A - ENSR00000541521 RegulatoryFeature regulatory_region_variant - - - - - - rs4266922 1:98385251 A ENSESTG00000008032 ENSESTT00000020336 Transcript intron_variant - - - - - - rs4266922 1:98385251 A ENSESTG00000008032 ENSESTT00000020357 Transcript intron_variant - - - - - - rs4266922 1:98385251 A ENSESTG00000008032 ENSESTT00000020349 Transcript intron_variant - - - - - - rs4266922 1:98385251 A 1806 NM_000110.3 Transcript intron_variant - - - - - - rs4266922 1:98385251 A CCDS30777.1 CCDS30777.1 Transcript intron_variant - - - - - - rs4266922 1:98385251 A 1806 NM_001160301.1 Transcript intron_variant - - - - - - rs4266922 1:98385251 A CCDS53346.1 CCDS53346.1 Transcript intron_variant - - - - - - rs9729838 1:98391364 T ENSESTG00000008032 ENSESTT00000020336 Transcript upstream_gene_variant - - - - - - DISTANCE=4759 rs9729838 1:98391364 T ENSESTG00000008032 ENSESTT00000020357 Transcript upstream_gene_variant - - - - - - DISTANCE=4789 rs9729838 1:98391364 T ENSESTG00000008032 ENSESTT00000020349 Transcript upstream_gene_variant - - - - - - DISTANCE=4774 rs9729838 1:98391364 T 1806 NM_000110.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4749 rs9729838 1:98391364 T CCDS30777.1 CCDS30777.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4886 rs9729838 1:98391364 T 1806 NM_001160301.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4749 rs9729838 1:98391364 T CCDS53346.1 CCDS53346.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4886 rs10783080 1:98408638 G - - - intergenic_variant - - - - - - rs4970726 1:98413096 C - - - intergenic_variant - - - - - - rs9699783 1:98420935 A - - - intergenic_variant - - - - - - rs355359 1:98591822 A ENSESTG00000008024 ENSESTT00000020276 Transcript intron_variant - - - - - - rs355355 1:98598375 T ENSESTG00000008024 ENSESTT00000020276 Transcript downstream_gene_variant - - - - - - DISTANCE=1001 rs355367 1:98609825 C - - - intergenic_variant - - - - - - rs822558 1:98655742 T - - - intergenic_variant - - - - - - rs698996 1:98660888 C - - - intergenic_variant - - - - - - rs303389 1:99591646 T 100129620 NR_033940.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs643139 1:99669474 A - - - intergenic_variant - - - - - - rs1536264 1:99783985 C - - - intergenic_variant - - - - - - rs1148351 1:99831216 T - - - intergenic_variant - - - - - - rs834995 1:100114532 T - ENSR00000541691 RegulatoryFeature regulatory_region_variant - - - - - - rs834995 1:100114532 T ENSESTG00000014478 ENSESTT00000036289 Transcript intron_variant - - - - - - rs834995 1:100114532 T 54873 NM_017734.4 Transcript intron_variant - - - - - - rs834995 1:100114532 T CCDS758.1 CCDS758.1 Transcript intron_variant - - - - - - rs11164353 1:102438729 G CCDS30781.1 CCDS30781.1 Transcript intron_variant - - - - - - rs11164353 1:102438729 G 118427 NM_058170.2 Transcript intron_variant - - - - - - rs11164353 1:102438729 G ENSESTG00000018097 ENSESTT00000045588 Transcript intron_variant - - - - - - rs10874534 1:102503921 G - - - intergenic_variant - - - - - - rs7545917 1:102525199 T - - - intergenic_variant - - - - - - rs4306152 1:102529257 T - - - intergenic_variant - - - - - - rs10782867 1:102538153 A - - - intergenic_variant - - - - - - rs10218555 1:102555142 C - - - intergenic_variant - - - - - - rs1878509 1:103011397 A - - - intergenic_variant - - - - - - rs2222160 1:103063731 C - - - intergenic_variant - - - - - - rs1376360 1:103122483 A - - - intergenic_variant - - - - - - rs2176420 1:103124847 A - - - intergenic_variant - - - - - - rs6675097 1:103134740 C - - - intergenic_variant - - - - - - rs1451035 1:103149092 T - - - intergenic_variant - - - - - - rs1451028 1:103170903 A - - - intergenic_variant - - - - - - rs7521833 1:103214572 C - - - intergenic_variant - - - - - - rs1823550 1:103221150 G - - - intergenic_variant - - - - - - rs6671708 1:103224114 C - - - intergenic_variant - - - - - - rs6577340 1:103389238 T CCDS53348.1 CCDS53348.1 Transcript intron_variant - - - - - - rs6577340 1:103389238 T 1301 NM_001854.3 Transcript intron_variant - - - - - - rs6577340 1:103389238 T ENSESTG00000004744 ENSESTT00000012004 Transcript intron_variant - - - - - - rs6577340 1:103389238 T 1301 NM_001190709.1 Transcript intron_variant - - - - - - rs6577340 1:103389238 T 1301 NM_080630.3 Transcript intron_variant - - - - - - rs6577340 1:103389238 T CCDS780.2 CCDS780.2 Transcript intron_variant - - - - - - rs6577340 1:103389238 T 1301 NM_080629.2 Transcript intron_variant - - - - - - rs6577340 1:103389238 T ENSESTG00000004744 ENSESTT00000012042 Transcript intron_variant - - - - - - rs6577340 1:103389238 T CCDS778.1 CCDS778.1 Transcript intron_variant - - - - - - rs6577340 1:103389238 T ENSESTG00000004744 ENSESTT00000012050 Transcript intron_variant - - - - - - rs6577340 1:103389238 T ENSESTG00000004744 ENSESTT00000012048 Transcript intron_variant - - - - - - rs4581295 1:103640017 A - - - intergenic_variant - - - - - - rs7414754 1:104090182 A ENSESTG00000033562 ENSESTT00000084935 Transcript intron_variant - - - - - - rs7414754 1:104090182 A ENSESTG00000033562 ENSESTT00000084953 Transcript intron_variant - - - - - - rs7414754 1:104090182 A 55599 NM_017619.3 Transcript intron_variant - - - - - - rs7414754 1:104090182 A ENSESTG00000033562 ENSESTT00000084958 Transcript intron_variant - - - - - - rs7414754 1:104090182 A ENSESTG00000033562 ENSESTT00000084943 Transcript intron_variant - - - - - - rs7414754 1:104090182 A ENSESTG00000033562 ENSESTT00000084916 Transcript intron_variant - - - - - - rs7414754 1:104090182 A CCDS781.1 CCDS781.1 Transcript intron_variant - - - - - - rs7414754 1:104090182 A ENSESTG00000033659 ENSESTT00000085074 Transcript intron_variant - - - - - - rs7414754 1:104090182 A ENSESTG00000033562 ENSESTT00000084937 Transcript intron_variant - - - - - - rs7414754 1:104090182 A ENSESTG00000033659 ENSESTT00000085078 Transcript intron_variant - - - - - - rs688143 1:104310211 C - - - intergenic_variant - - - - - - rs9435616 1:104498044 A - - - intergenic_variant - - - - - - rs10736048 1:104708448 T - - - intergenic_variant - - - - - - rs4847157 1:104710425 G - - - intergenic_variant - - - - - - rs4847158 1:104710546 G - - - intergenic_variant - - - - - - rs4500329 1:104857220 A - - - intergenic_variant - - - - - - rs316940 1:105109668 T - - - intergenic_variant - - - - - - rs6583089 1:105405214 C - ENSR00001523126 RegulatoryFeature regulatory_region_variant - - - - - - rs6583089 1:105405214 C - - - intergenic_variant - - - - - - rs11184336 1:105418675 T - - - intergenic_variant - - - - - - rs2502914 1:105947336 T - - - intergenic_variant - - - - - - rs2502911 1:105955848 T - - - intergenic_variant - - - - - - rs777100 1:106055852 T - - - intergenic_variant - - - - - - rs1721564 1:106071597 A - - - intergenic_variant - - - - - - rs1710789 1:106072624 C - - - intergenic_variant - - - - - - rs7417608 1:106136030 C ENSESTG00000017324 ENSESTT00000043567 Transcript intron_variant - - - - - - rs3004232 1:106502267 C ENSESTG00000017295 ENSESTT00000043451 Transcript intron_variant - - - - - - rs4565745 1:107272503 G - - - intergenic_variant - - - - - - rs1401834 1:107359829 T ENSESTG00000005415 ENSESTT00000013744 Transcript upstream_gene_variant - - - - - - DISTANCE=1032 rs4466686 1:107386757 C - - - intergenic_variant - - - - - - rs2504459 1:108229072 C 10451 NM_001079874.1 Transcript intron_variant - - - - - - rs2504459 1:108229072 C ENSESTG00000032510 ENSESTT00000082112 Transcript intron_variant - - - - - - rs2504459 1:108229072 C CCDS785.1 CCDS785.1 Transcript intron_variant - - - - - - rs2504459 1:108229072 C ENSESTG00000032510 ENSESTT00000082106 Transcript intron_variant - - - - - - rs2504459 1:108229072 C CCDS44181.1 CCDS44181.1 Transcript intron_variant - - - - - - rs2504459 1:108229072 C ENSESTG00000032510 ENSESTT00000082093 Transcript intron_variant - - - - - - rs2504459 1:108229072 C 10451 NM_006113.4 Transcript intron_variant - - - - - - rs1419002 1:108617078 C ENSESTG00000032477 ENSESTT00000081977 Transcript 3_prime_UTR_variant 471 - - - - - rs10785841 1:108872493 G ENSESTG00000017349 ENSESTT00000043641 Transcript intron_variant - - - - - - rs2647483 1:109075299 C - - - intergenic_variant - - - - - - rs6671743 1:110576282 A ENSESTG00000030215 ENSESTT00000076344 Transcript upstream_gene_variant - - - - - - DISTANCE=966 rs6671743 1:110576282 A ENSESTG00000030215 ENSESTT00000076300 Transcript upstream_gene_variant - - - - - - DISTANCE=961 rs6671743 1:110576282 A ENSESTG00000030215 ENSESTT00000076319 Transcript upstream_gene_variant - - - - - - DISTANCE=961 rs6671743 1:110576282 A 85369 NM_033088.2 Transcript upstream_gene_variant - - - - - - DISTANCE=959 rs6671743 1:110576282 A CCDS30798.1 CCDS30798.1 Transcript upstream_gene_variant - - - - - - DISTANCE=978 rs6671743 1:110576282 A ENSESTG00000030215 ENSESTT00000076332 Transcript upstream_gene_variant - - - - - - DISTANCE=961 rs641400 1:110840276 C 440600 NR_036595.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs632132 1:110851391 G 440600 NR_036595.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2640481 1:111212117 A 3738 NM_002232.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2193 rs2640481 1:111212117 A CCDS828.2 CCDS828.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3587 rs2640481 1:111212117 A ENSESTG00000004603 ENSESTT00000011603 Transcript intron_variant - - - - - - rs1908095 1:111227715 G - - - intergenic_variant - - - - - - rs1782824 1:111581549 T - - - intergenic_variant - - - - - - rs2764551 1:111784148 G ENSESTG00000004893 ENSESTT00000012457 Transcript upstream_gene_variant - - - - - - DISTANCE=695 rs2764551 1:111784148 G CCDS41367.1 CCDS41367.1 Transcript intron_variant - - - - - - rs2764551 1:111784148 G CCDS30803.1 CCDS30803.1 Transcript intron_variant - - - - - - rs2764551 1:111784148 G ENSESTG00000004869 ENSESTT00000012424 Transcript downstream_gene_variant - - - - - - DISTANCE=163 rs2764551 1:111784148 G ENSESTG00000004869 ENSESTT00000012386 Transcript downstream_gene_variant - - - - - - DISTANCE=2595 rs2764551 1:111784148 G 1117 NM_004000.2 Transcript intron_variant - - - - - - rs2764551 1:111784148 G 1117 NM_001025199.1 Transcript intron_variant - - - - - - rs2764551 1:111784148 G ENSESTG00000004869 ENSESTT00000012401 Transcript downstream_gene_variant - - - - - - DISTANCE=2689 rs2764551 1:111784148 G 1117 NM_001025197.1 Transcript intron_variant - - - - - - rs2764551 1:111784148 G ENSESTG00000004893 ENSESTT00000012454 Transcript intron_variant - - - - - - rs2764551 1:111784148 G CCDS30802.1 CCDS30802.1 Transcript intron_variant - - - - - - rs2211494 1:112020238 C ENSESTG00000004984 ENSESTT00000012652 Transcript intron_variant - - - - - - rs2211494 1:112020238 C 128346 NM_174896.2 Transcript intron_variant - - - - - - rs2211494 1:112020238 C ENSESTG00000004984 ENSESTT00000012656 Transcript intron_variant - - - - - - rs2211494 1:112020238 C CCDS837.1 CCDS837.1 Transcript intron_variant - - - - - - rs945965 1:112074915 C 140 NM_001081976.1 Transcript intron_variant - - - - - - rs945965 1:112074915 C CCDS41369.1 CCDS41369.1 Transcript intron_variant - - - - - - rs945965 1:112074915 C ENSESTG00000005082 ENSESTT00000012924 Transcript intron_variant - - - - - - rs945965 1:112074915 C ENSESTG00000005082 ENSESTT00000012929 Transcript intron_variant - - - - - - rs2800884 1:112143696 A - ENSR00000542684 RegulatoryFeature regulatory_region_variant - - - - - - rs2800884 1:112143696 A 100129269 NR_034126.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs197405 1:112304126 T ENSESTG00000005027 ENSESTT00000012810 Transcript intron_variant - - - - - - rs197405 1:112304126 T ENSESTG00000005027 ENSESTT00000012816 Transcript intron_variant - - - - - - rs197405 1:112304126 T 11218 NM_007204.4 Transcript intron_variant - - - - - - rs197405 1:112304126 T ENSESTG00000005027 ENSESTT00000012818 Transcript intron_variant - - - - - - rs197405 1:112304126 T ENSESTG00000005027 ENSESTT00000012809 Transcript intron_variant - - - - - - rs197405 1:112304126 T CCDS842.1 CCDS842.1 Transcript intron_variant - - - - - - rs197405 1:112304126 T ENSESTG00000005027 ENSESTT00000012823 Transcript upstream_gene_variant - - - - - - DISTANCE=1396 rs2813869 1:112354619 G CCDS844.1 CCDS844.1 Transcript intron_variant - - - - - - rs2813869 1:112354619 G ENSESTG00000005062 ENSESTT00000012869 Transcript intron_variant - - - - - - rs2813869 1:112354619 G CCDS843.1 CCDS843.1 Transcript intron_variant - - - - - - rs2813869 1:112354619 G 3752 NM_004980.4 Transcript intron_variant - - - - - - rs2813869 1:112354619 G 3752 NM_172198.2 Transcript intron_variant - - - - - - rs2120435 1:112478789 G CCDS844.1 CCDS844.1 Transcript intron_variant - - - - - - rs2120435 1:112478789 G ENSESTG00000005062 ENSESTT00000012869 Transcript intron_variant - - - - - - rs2120435 1:112478789 G CCDS843.1 CCDS843.1 Transcript intron_variant - - - - - - rs2120435 1:112478789 G 3752 NM_004980.4 Transcript intron_variant - - - - - - rs2120435 1:112478789 G ENSESTG00000005056 ENSESTT00000012861 Transcript intron_variant - - - - - - rs2120435 1:112478789 G 3752 NM_172198.2 Transcript intron_variant - - - - - - rs1947041 1:112494037 C CCDS844.1 CCDS844.1 Transcript intron_variant - - - - - - rs1947041 1:112494037 C ENSESTG00000005062 ENSESTT00000012869 Transcript intron_variant - - - - - - rs1947041 1:112494037 C CCDS843.1 CCDS843.1 Transcript intron_variant - - - - - - rs1947041 1:112494037 C 3752 NM_004980.4 Transcript intron_variant - - - - - - rs1947041 1:112494037 C ENSESTG00000005056 ENSESTT00000012861 Transcript intron_variant - - - - - - rs1947041 1:112494037 C 3752 NM_172198.2 Transcript intron_variant - - - - - - rs6658045 1:112499983 G CCDS844.1 CCDS844.1 Transcript intron_variant - - - - - - rs6658045 1:112499983 G ENSESTG00000005062 ENSESTT00000012869 Transcript intron_variant - - - - - - rs6658045 1:112499983 G CCDS843.1 CCDS843.1 Transcript intron_variant - - - - - - rs6658045 1:112499983 G 3752 NM_004980.4 Transcript intron_variant - - - - - - rs6658045 1:112499983 G ENSESTG00000005056 ENSESTT00000012861 Transcript intron_variant - - - - - - rs6658045 1:112499983 G 3752 NM_172198.2 Transcript intron_variant - - - - - - rs269096 1:112635062 T - - - intergenic_variant - - - - - - rs6680732 1:113136776 C CCDS852.1 CCDS852.1 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089552 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089547 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089549 Transcript intron_variant - - - - - - rs6680732 1:113136776 C CCDS849.1 CCDS849.1 Transcript intron_variant - - - - - - rs6680732 1:113136776 C CCDS848.1 CCDS848.1 Transcript intron_variant - - - - - - rs6680732 1:113136776 C 54879 NM_017744.4 Transcript intron_variant - - - - - - rs6680732 1:113136776 C CCDS850.1 CCDS850.1 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089546 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089554 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089551 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089544 Transcript intron_variant - - - - - - rs6680732 1:113136776 C 54879 NM_138728.2 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089543 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089550 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089527 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089560 Transcript intron_variant - - - - - - rs6680732 1:113136776 C 54879 NM_138729.3 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089541 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089561 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089556 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089545 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089542 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089558 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089531 Transcript intron_variant - - - - - - rs6680732 1:113136776 C 54879 NM_138727.3 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089559 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089523 Transcript intron_variant - - - - - - rs6680732 1:113136776 C ENSESTG00000035449 ENSESTT00000089548 Transcript intron_variant - - - - - - rs1216887 1:113737527 C 643441 NR_038846.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1876 rs1082074 1:113856527 G - - - intergenic_variant - - - - - - rs530970 1:114614925 T - - - intergenic_variant - - - - - - rs209880 1:114775912 C - - - intergenic_variant - - - - - - rs502665 1:114828575 C - - - intergenic_variant - - - - - - rs1230795 1:114947935 A ENSESTG00000015895 ENSESTT00000039921 Transcript downstream_gene_variant - - - - - - DISTANCE=4872 rs1230795 1:114947935 A 51592 NM_015906.3 Transcript intron_variant - - - - - - rs1230795 1:114947935 A CCDS872.1 CCDS872.1 Transcript intron_variant - - - - - - rs1230795 1:114947935 A ENSESTG00000015895 ENSESTT00000039927 Transcript downstream_gene_variant - - - - - - DISTANCE=4872 rs1230795 1:114947935 A CCDS873.1 CCDS873.1 Transcript intron_variant - - - - - - rs1230795 1:114947935 A 51592 NM_033020.2 Transcript intron_variant - - - - - - rs1230795 1:114947935 A ENSESTG00000015895 ENSESTT00000039971 Transcript downstream_gene_variant - - - - - - DISTANCE=1682 rs1230795 1:114947935 A ENSESTG00000015895 ENSESTT00000039976 Transcript downstream_gene_variant - - - - - - DISTANCE=4748 rs6660976 1:115008992 C - ENSR00000670819 RegulatoryFeature regulatory_region_variant - - - - - - rs6660976 1:115008992 C ENSESTG00000015895 ENSESTT00000039921 Transcript intron_variant - - - - - - rs6660976 1:115008992 C 51592 NM_015906.3 Transcript intron_variant - - - - - - rs6660976 1:115008992 C CCDS872.1 CCDS872.1 Transcript intron_variant - - - - - - rs6660976 1:115008992 C ENSESTG00000015895 ENSESTT00000039927 Transcript intron_variant - - - - - - rs6660976 1:115008992 C CCDS873.1 CCDS873.1 Transcript intron_variant - - - - - - rs6660976 1:115008992 C ENSESTG00000015895 ENSESTT00000039933 Transcript intron_variant - - - - - - rs6660976 1:115008992 C ENSESTG00000015895 ENSESTT00000039925 Transcript intron_variant - - - - - - rs6660976 1:115008992 C 51592 NM_033020.2 Transcript intron_variant - - - - - - rs6695458 1:115034056 T ENSESTG00000015895 ENSESTT00000039921 Transcript intron_variant - - - - - - rs6695458 1:115034056 T 51592 NM_015906.3 Transcript intron_variant - - - - - - rs6695458 1:115034056 T CCDS872.1 CCDS872.1 Transcript intron_variant - - - - - - rs6695458 1:115034056 T ENSESTG00000015895 ENSESTT00000039927 Transcript intron_variant - - - - - - rs6695458 1:115034056 T CCDS873.1 CCDS873.1 Transcript intron_variant - - - - - - rs6695458 1:115034056 T ENSESTG00000015895 ENSESTT00000039933 Transcript intron_variant - - - - - - rs6695458 1:115034056 T ENSESTG00000015895 ENSESTT00000039925 Transcript intron_variant - - - - - - rs6695458 1:115034056 T 51592 NM_033020.2 Transcript intron_variant - - - - - - rs10776785 1:115040213 G ENSESTG00000015895 ENSESTT00000039921 Transcript intron_variant - - - - - - rs10776785 1:115040213 G 51592 NM_015906.3 Transcript intron_variant - - - - - - rs10776785 1:115040213 G CCDS872.1 CCDS872.1 Transcript intron_variant - - - - - - rs10776785 1:115040213 G ENSESTG00000015895 ENSESTT00000039927 Transcript upstream_gene_variant - - - - - - DISTANCE=1263 rs10776785 1:115040213 G CCDS873.1 CCDS873.1 Transcript intron_variant - - - - - - rs10776785 1:115040213 G ENSESTG00000015895 ENSESTT00000039933 Transcript upstream_gene_variant - - - - - - DISTANCE=1263 rs10776785 1:115040213 G ENSESTG00000015895 ENSESTT00000039925 Transcript intron_variant - - - - - - rs10776785 1:115040213 G 51592 NM_033020.2 Transcript intron_variant - - - - - - rs7544996 1:115178569 T ENSESTG00000015860 ENSESTT00000039774 Transcript intron_variant - - - - - - rs7544996 1:115178569 T 163259 NM_001256404.1 Transcript intron_variant - - - - - - rs7544996 1:115178569 T 163259 NM_198459.3 Transcript intron_variant - - - - - - rs7544996 1:115178569 T ENSESTG00000015860 ENSESTT00000039779 Transcript intron_variant - - - - - - rs7544776 1:115296984 C ENSESTG00000015728 ENSESTT00000039534 Transcript intron_variant - - - - - - rs7544776 1:115296984 C 7812 NM_001242892.1 Transcript intron_variant - - - - - - rs7544776 1:115296984 C 7812 NM_001242891.1 Transcript intron_variant - - - - - - rs7544776 1:115296984 C ENSESTG00000015728 ENSESTT00000039528 Transcript intron_variant - - - - - - rs7544776 1:115296984 C ENSESTG00000015728 ENSESTT00000039519 Transcript intron_variant - - - - - - rs7544776 1:115296984 C 7812 NM_007158.5 Transcript intron_variant - - - - - - rs7544776 1:115296984 C 7812 NM_001007553.2 Transcript intron_variant - - - - - - rs7544776 1:115296984 C 7812 NM_001242893.1 Transcript intron_variant - - - - - - rs7544776 1:115296984 C ENSESTG00000015728 ENSESTT00000039505 Transcript intron_variant - - - - - - rs7544776 1:115296984 C ENSESTG00000015728 ENSESTT00000039486 Transcript intron_variant - - - - - - rs7544776 1:115296984 C 7812 NM_001130523.2 Transcript intron_variant - - - - - - rs7544776 1:115296984 C ENSESTG00000015728 ENSESTT00000039458 Transcript intron_variant - - - - - - rs7544776 1:115296984 C ENSESTG00000015728 ENSESTT00000039473 Transcript intron_variant - - - - - - rs360657 1:115453701 T ENSESTG00000015551 ENSESTT00000039055 Transcript intron_variant - - - - - - rs360657 1:115453701 T ENSESTG00000015551 ENSESTT00000039034 Transcript intron_variant - - - - - - rs360657 1:115453701 T CCDS879.1 CCDS879.1 Transcript intron_variant - - - - - - rs360657 1:115453701 T 6847 NM_003176.2 Transcript intron_variant - - - - - - rs360657 1:115453701 T ENSESTG00000015551 ENSESTT00000039059 Transcript intron_variant - - - - - - rs1286348 1:115612089 T - ENSR00001523705 RegulatoryFeature regulatory_region_variant - - - - - - rs1286348 1:115612089 T CCDS881.1 CCDS881.1 Transcript intron_variant - - - - - - rs1286348 1:115612089 T ENSESTG00000015704 ENSESTT00000039338 Transcript intron_variant - - - - - - rs1286348 1:115612089 T ENSESTG00000015704 ENSESTT00000039341 Transcript intron_variant - - - - - - rs1286348 1:115612089 T 10100 NM_005725.4 Transcript intron_variant - - - - - - rs1286348 1:115612089 T ENSESTG00000015704 ENSESTT00000039311 Transcript intron_variant - - - - - - rs10745348 1:115803815 G - - - intergenic_variant - - - - - - rs4417063 1:115853046 C 4803 NM_002506.2 Transcript intron_variant - - - - - - rs4417063 1:115853046 C ENSESTG00000003596 ENSESTT00000008999 Transcript intron_variant - - - - - - rs4328071 1:116091366 C - - - intergenic_variant - - - - - - rs3017126 1:116095555 T - - - intergenic_variant - - - - - - rs3017131 1:116100333 G - - - intergenic_variant - - - - - - rs3017152 1:116110194 C - - - intergenic_variant - - - - - - rs4839466 1:116178548 T - - - intergenic_variant - - - - - - rs11579827 1:116710800 G - ENSR00000166341 RegulatoryFeature regulatory_region_variant - - - - - - rs11579827 1:116710800 G - - - intergenic_variant - - - - - - rs2491115 1:117454823 G - ENSR00000166376 RegulatoryFeature regulatory_region_variant - - - - - - rs2491115 1:117454823 G 5738 NM_020440.2 Transcript intron_variant - - - - - - rs2491115 1:117454823 G CCDS890.1 CCDS890.1 Transcript intron_variant - - - - - - rs2491115 1:117454823 G ENSESTG00000019623 ENSESTT00000049399 Transcript intron_variant - - - - - - rs1146285 1:117810713 A - - - intergenic_variant - - - - - - rs184384 1:118210014 T - - - intergenic_variant - - - - - - rs319480 1:118239108 T - ENSR00001039858 RegulatoryFeature regulatory_region_variant - - - - - - rs319480 1:118239108 T - - - intergenic_variant - - - - - - rs10733098 1:118484265 A ENSESTG00000017069 ENSESTT00000042883 Transcript intron_variant - - - - - - rs10733098 1:118484265 A ENSESTG00000017079 ENSESTT00000042989 Transcript upstream_gene_variant - - - - - - DISTANCE=883 rs10733098 1:118484265 A ENSESTG00000017079 ENSESTT00000042983 Transcript upstream_gene_variant - - - - - - DISTANCE=883 rs10733098 1:118484265 A ENSESTG00000017043 ENSESTT00000042871 Transcript downstream_gene_variant - - - - - - DISTANCE=4833 rs10733098 1:118484265 A ENSESTG00000017079 ENSESTT00000042999 Transcript upstream_gene_variant - - - - - - DISTANCE=883 rs10733098 1:118484265 A 10885 NM_006784.2 Transcript intron_variant - - - - - - rs10733098 1:118484265 A CCDS898.1 CCDS898.1 Transcript intron_variant - - - - - - rs10733098 1:118484265 A ENSESTG00000017043 ENSESTT00000042856 Transcript downstream_gene_variant - - - - - - DISTANCE=3136 rs2180767 1:118905676 C - - - intergenic_variant - - - - - - rs2145416 1:118905802 C - - - intergenic_variant - - - - - - rs2145415 1:118905970 T - - - intergenic_variant - - - - - - rs2493803 1:118907274 C - - - intergenic_variant - - - - - - rs1229125 1:118999938 G - - - intergenic_variant - - - - - - rs6698301 1:119614391 A CCDS900.1 CCDS900.1 Transcript intron_variant - - - - - - rs6698301 1:119614391 A ENSESTG00000019792 ENSESTT00000049662 Transcript intron_variant - - - - - - rs6698301 1:119614391 A CCDS30817.1 CCDS30817.1 Transcript intron_variant - - - - - - rs6698301 1:119614391 A ENSESTG00000019792 ENSESTT00000049649 Transcript intron_variant - - - - - - rs6698301 1:119614391 A 10352 NM_015836.3 Transcript intron_variant - - - - - - rs6698301 1:119614391 A ENSESTG00000019792 ENSESTT00000049668 Transcript intron_variant - - - - - - rs6698301 1:119614391 A 10352 NM_201263.2 Transcript intron_variant - - - - - - rs2039967 1:119737907 A ENSESTG00000013866 ENSESTT00000034630 Transcript intron_variant - - - - - - rs3122962 1:142709643 T 100874392 NR_046228.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs833392 1:145438578 A - ENSR00000670982 RegulatoryFeature regulatory_region_variant - - - - - - rs833392 1:145438578 A ENSESTG00000034308 ENSESTT00000086755 Transcript upstream_gene_variant - - - - - - DISTANCE=20 rs833392 1:145438578 A CCDS913.1 CCDS913.1 Transcript upstream_gene_variant - - - - - - DISTANCE=225 rs833392 1:145438578 A 10628 NM_006472.3 Transcript 5_prime_UTR_variant 117 - - - - - rs833392 1:145438578 A ENSESTG00000034308 ENSESTT00000086781 Transcript upstream_gene_variant - - - - - - DISTANCE=937 rs2017489 1:146574189 C ENSESTG00000021849 ENSESTT00000054939 Transcript intron_variant - - - - - - rs7519819 1:150775329 G 1513 NM_000396.3 Transcript intron_variant - - - - - - rs7519819 1:150775329 G CCDS969.1 CCDS969.1 Transcript intron_variant - - - - - - rs7519819 1:150775329 G ENSESTG00000028546 ENSESTT00000071767 Transcript intron_variant - - - - - - rs7519819 1:150775329 G ENSESTG00000028546 ENSESTT00000071907 Transcript intron_variant - - - - - - rs267737 1:150944541 G - ENSR00000544830 RegulatoryFeature regulatory_region_variant - - - - - - rs267737 1:150944541 G ENSESTG00000028253 ENSESTT00000071388 Transcript intron_variant - - - - - - rs267737 1:150944541 G ENSESTG00000028253 ENSESTT00000071376 Transcript intron_variant - - - - - - rs267737 1:150944541 G 29956 NM_181746.3 Transcript intron_variant - - - - - - rs267737 1:150944541 G ENSESTG00000028253 ENSESTT00000071339 Transcript intron_variant - - - - - - rs267737 1:150944541 G ENSESTG00000028253 ENSESTT00000071349 Transcript intron_variant - - - - - - rs267737 1:150944541 G 29956 NM_022075.4 Transcript intron_variant - - - - - - rs267737 1:150944541 G ENSESTG00000026730 ENSESTT00000067296 Transcript upstream_gene_variant - - - - - - DISTANCE=1058 rs267737 1:150944541 G CCDS973.1 CCDS973.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2975 rs267737 1:150944541 G ENSESTG00000028253 ENSESTT00000071365 Transcript intron_variant - - - - - - rs4971001 1:151097716 C - - - intergenic_variant - - - - - - rs4845326 1:151675414 G CCDS1002.1 CCDS1002.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2103 rs4845326 1:151675414 G ENSESTG00000024243 ENSESTT00000061365 Transcript downstream_gene_variant - - - - - - DISTANCE=4300 rs4845326 1:151675414 G 11189 NM_007185.4 Transcript 3_prime_UTR_variant 2713 - - - - - rs4845326 1:151675414 G 11189 NM_001172649.1 Transcript 3_prime_UTR_variant 2155 - - - - - rs4845326 1:151675414 G 11189 NM_001172648.1 Transcript 3_prime_UTR_variant 2472 - - - - - rs4845326 1:151675414 G 81609 NM_030918.5 Transcript downstream_gene_variant - - - - - - DISTANCE=3855 rs4845326 1:151675414 G CCDS53367.1 CCDS53367.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2103 rs2495397 1:151740666 C 11022 NM_006862.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3374 rs2495397 1:151740666 C CCDS58028.1 CCDS58028.1 Transcript synonymous_variant 301 301 101 L Ttg/Ctg - rs2495397 1:151740666 C ENSESTG00000024212 ENSESTT00000061190 Transcript downstream_gene_variant - - - - - - DISTANCE=2053 rs2495397 1:151740666 C 51686 NM_016178.2 Transcript missense_variant 504 437 146 L/P cTt/cCt - rs2495397 1:151740666 C ENSESTG00000023559 ENSESTT00000059480 Transcript upstream_gene_variant - - - - - - DISTANCE=13 rs2495397 1:151740666 C ENSESTG00000023559 ENSESTT00000059433 Transcript synonymous_variant 356 241 81 L Ttg/Ctg - rs2495397 1:151740666 C 51686 NM_001134939.1 Transcript missense_variant 469 302 101 L/P cTt/cCt - rs2495397 1:151740666 C ENSESTG00000023559 ENSESTT00000059446 Transcript downstream_gene_variant - - - - - - DISTANCE=679 rs2495397 1:151740666 C ENSESTG00000024212 ENSESTT00000061250 Transcript downstream_gene_variant - - - - - - DISTANCE=2006 rs2495397 1:151740666 C 65005 NM_031420.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4626 rs2495397 1:151740666 C CCDS1003.1 CCDS1003.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4711 rs2495397 1:151740666 C ENSESTG00000023559 ENSESTT00000059455 Transcript synonymous_variant 467 241 81 L Ttg/Ctg - rs2495397 1:151740666 C ENSESTG00000023559 ENSESTT00000059468 Transcript intron_variant - - - - - - rs6587618 1:151752943 T 11022 NM_006862.3 Transcript intron_variant - - - - - - rs6587618 1:151752943 T ENSESTG00000024212 ENSESTT00000061190 Transcript upstream_gene_variant - - - - - - DISTANCE=1608 rs6587618 1:151752943 T ENSESTG00000024143 ENSESTT00000061118 Transcript intron_variant - - - - - - rs6587618 1:151752943 T ENSESTG00000024143 ENSESTT00000061134 Transcript intron_variant - - - - - - rs6587618 1:151752943 T CCDS41394.1 CCDS41394.1 Transcript intron_variant - - - - - - rs6587618 1:151752943 T 11022 NM_001083963.1 Transcript intron_variant - - - - - - rs6587618 1:151752943 T ENSESTG00000024143 ENSESTT00000061172 Transcript intron_variant - - - - - - rs6587618 1:151752943 T ENSESTG00000024212 ENSESTT00000061250 Transcript upstream_gene_variant - - - - - - DISTANCE=4595 rs6587618 1:151752943 T 11022 NM_001083965.1 Transcript intron_variant - - - - - - rs6587618 1:151752943 T CCDS41395.1 CCDS41395.1 Transcript intron_variant - - - - - - rs6587618 1:151752943 T 11022 NM_001083964.1 Transcript intron_variant - - - - - - rs6587618 1:151752943 T ENSESTG00000024143 ENSESTT00000061151 Transcript intron_variant - - - - - - rs1332496 1:152681543 C CCDS1022.1 CCDS1022.1 Transcript upstream_gene_variant - - - - - - DISTANCE=9 rs1332496 1:152681543 C 199834 NM_178356.2 Transcript 5_prime_UTR_variant 21 - - - - - rs6695127 1:152721460 C - - - intergenic_variant - - - - - - rs6682664 1:152810128 A - - - intergenic_variant - - - - - - rs1576291 1:153302072 T CCDS30871.1 CCDS30871.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1171 rs1576291 1:153302072 T 57115 NM_020393.2 Transcript downstream_gene_variant - - - - - - DISTANCE=524 rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030744 Transcript intron_variant - - - - - - rs4845571 1:153738555 C CCDS1052.1 CCDS1052.1 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030750 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030655 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030696 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030680 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030736 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030731 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030719 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030674 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030766 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030684 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030754 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030761 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030768 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030735 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030723 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030771 Transcript upstream_gene_variant - - - - - - DISTANCE=1375 rs4845571 1:153738555 C 65123 NM_023015.3 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030777 Transcript upstream_gene_variant - - - - - - DISTANCE=1375 rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030727 Transcript intron_variant - - - - - - rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030782 Transcript upstream_gene_variant - - - - - - DISTANCE=4601 rs4845571 1:153738555 C ENSESTG00000012209 ENSESTT00000030698 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs7544828 1:153931381 G - ENSR00000166755 RegulatoryFeature regulatory_region_variant - - - - - - rs7544828 1:153931381 G ENSESTG00000012705 ENSESTT00000031934 Transcript upstream_gene_variant - - - - - - DISTANCE=291 rs7544828 1:153931381 G ENSESTG00000012705 ENSESTT00000031904 Transcript downstream_gene_variant - - - - - - DISTANCE=1754 rs7544828 1:153931381 G ENSESTG00000012705 ENSESTT00000031900 Transcript downstream_gene_variant - - - - - - DISTANCE=3340 rs7544828 1:153931381 G CCDS30875.1 CCDS30875.1 Transcript upstream_gene_variant - - - - - - DISTANCE=408 rs7544828 1:153931381 G ENSESTG00000012309 ENSESTT00000030869 Transcript upstream_gene_variant - - - - - - DISTANCE=337 rs7544828 1:153931381 G ENSESTG00000012705 ENSESTT00000031912 Transcript intron_variant - - - - - - rs7544828 1:153931381 G CCDS1055.1 CCDS1055.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1193 rs7544828 1:153931381 G ENSESTG00000012705 ENSESTT00000031923 Transcript upstream_gene_variant - - - - - - DISTANCE=249 rs7544828 1:153931381 G ENSESTG00000012304 ENSESTT00000030853 Transcript downstream_gene_variant - - - - - - DISTANCE=283 rs7544828 1:153931381 G 200186 NM_181715.2 Transcript upstream_gene_variant - - - - - - DISTANCE=249 rs7544828 1:153931381 G 27173 NM_014437.3 Transcript downstream_gene_variant - - - - - - DISTANCE=207 rs2066135 1:154061855 G 91181 NM_207308.2 Transcript intron_variant - - - - - - rs2066135 1:154061855 G 91181 NM_001159484.1 Transcript intron_variant - - - - - - rs2066135 1:154061855 G CCDS53370.1 CCDS53370.1 Transcript intron_variant - - - - - - rs2066135 1:154061855 G ENSESTG00000012681 ENSESTT00000031831 Transcript intron_variant - - - - - - rs2066135 1:154061855 G CCDS41399.1 CCDS41399.1 Transcript intron_variant - - - - - - rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031259 Transcript upstream_gene_variant - - - - - - DISTANCE=1757 rs9804042 1:154191641 T 25912 NM_138740.2 Transcript intron_variant - - - - - - rs9804042 1:154191641 T CCDS41404.1 CCDS41404.1 Transcript intron_variant - - - - - - rs9804042 1:154191641 T CCDS1062.1 CCDS1062.1 Transcript intron_variant - - - - - - rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031227 Transcript upstream_gene_variant - - - - - - DISTANCE=1007 rs9804042 1:154191641 T CCDS1061.1 CCDS1061.1 Transcript intron_variant - - - - - - rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031249 Transcript upstream_gene_variant - - - - - - DISTANCE=1631 rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031237 Transcript upstream_gene_variant - - - - - - DISTANCE=1007 rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031232 Transcript upstream_gene_variant - - - - - - DISTANCE=1007 rs9804042 1:154191641 T 25912 NM_015449.2 Transcript intron_variant - - - - - - rs9804042 1:154191641 T 9898 NM_014847.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1684 rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031268 Transcript upstream_gene_variant - - - - - - DISTANCE=1790 rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031250 Transcript upstream_gene_variant - - - - - - DISTANCE=1631 rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031257 Transcript upstream_gene_variant - - - - - - DISTANCE=1757 rs9804042 1:154191641 T 9898 NM_001127320.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1014 rs9804042 1:154191641 T ENSESTG00000012630 ENSESTT00000031675 Transcript intron_variant - - - - - - rs9804042 1:154191641 T 25912 NM_001098616.1 Transcript intron_variant - - - - - - rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031262 Transcript upstream_gene_variant - - - - - - DISTANCE=1790 rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031239 Transcript upstream_gene_variant - - - - - - DISTANCE=1007 rs9804042 1:154191641 T ENSESTG00000012415 ENSESTT00000031261 Transcript upstream_gene_variant - - - - - - DISTANCE=1790 rs1685608 1:154278272 A - - - intergenic_variant - - - - - - rs2481066 1:154326990 C - ENSR00001524890 RegulatoryFeature regulatory_region_variant - - - - - - rs2481066 1:154326990 C 57198 NM_020452.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3210 rs7553572 1:154682873 C 3782 NM_002249.5 Transcript intron_variant - - - - - - rs7553572 1:154682873 C CCDS30880.1 CCDS30880.1 Transcript intron_variant - - - - - - rs7553572 1:154682873 C 3782 NM_001204087.1 Transcript intron_variant - - - - - - rs7553572 1:154682873 C ENSESTG00000014567 ENSESTT00000036508 Transcript intron_variant - - - - - - rs7553572 1:154682873 C CCDS1072.1 CCDS1072.1 Transcript intron_variant - - - - - - rs7553572 1:154682873 C ENSESTG00000014567 ENSESTT00000036493 Transcript intron_variant - - - - - - rs7553572 1:154682873 C 3782 NM_170782.2 Transcript intron_variant - - - - - - rs2016850 1:154709948 A 3782 NM_002249.5 Transcript intron_variant - - - - - - rs2016850 1:154709948 A 3782 NM_001204087.1 Transcript intron_variant - - - - - - rs2016850 1:154709948 A ENSESTG00000014567 ENSESTT00000036508 Transcript intron_variant - - - - - - rs2016850 1:154709948 A ENSESTG00000014567 ENSESTT00000036469 Transcript intron_variant - - - - - - rs2016850 1:154709948 A CCDS30880.1 CCDS30880.1 Transcript intron_variant - - - - - - rs2016850 1:154709948 A CCDS1072.1 CCDS1072.1 Transcript intron_variant - - - - - - rs2016850 1:154709948 A 3782 NM_170782.2 Transcript intron_variant - - - - - - rs2016850 1:154709948 A ENSESTG00000014567 ENSESTT00000036493 Transcript intron_variant - - - - - - rs2016850 1:154709948 A ENSESTG00000014567 ENSESTT00000036515 Transcript intron_variant - - - - - - rs1566967 1:154857366 A - ENSR00000545449 RegulatoryFeature regulatory_region_variant - - - - - - rs1566967 1:154857366 A - - - intergenic_variant - - - - - - rs7536751 1:154998153 C 127579 NM_144622.2 Transcript intron_variant - - - - - - rs7536751 1:154998153 C ENSESTG00000014433 ENSESTT00000036155 Transcript intron_variant - - - - - - rs7536751 1:154998153 C CCDS1082.2 CCDS1082.2 Transcript intron_variant - - - - - - rs7536751 1:154998153 C ENSESTG00000014433 ENSESTT00000036160 Transcript upstream_gene_variant - - - - - - DISTANCE=1807 rs7536751 1:154998153 C ENSESTG00000014433 ENSESTT00000036145 Transcript intron_variant - - - - - - rs6677756 1:155195044 G - ENSR00000545531 RegulatoryFeature regulatory_region_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000013986 ENSESTT00000034983 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035468 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035433 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035537 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035524 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014391 ENSESTT00000036001 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035551 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035515 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000013999 ENSESTT00000035004 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035511 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035540 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035530 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035476 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035458 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035371 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035533 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035455 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035443 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035545 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035418 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035489 Transcript intron_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035453 Transcript intron_variant - - - - - - rs6677756 1:155195044 G 2630 NR_002188.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs6677756 1:155195044 G ENSESTG00000014147 ENSESTT00000035547 Transcript intron_variant - - - - - - rs822480 1:155797432 T CCDS1121.1 CCDS1121.1 Transcript intron_variant - - - - - - rs822480 1:155797432 T CCDS44242.1 CCDS44242.1 Transcript intron_variant - - - - - - rs822480 1:155797432 T ENSESTG00000014369 ENSESTT00000035933 Transcript intron_variant - - - - - - rs822480 1:155797432 T 54856 NM_032292.4 Transcript intron_variant - - - - - - rs822480 1:155797432 T ENSESTG00000014369 ENSESTT00000035988 Transcript intron_variant - - - - - - rs822480 1:155797432 T 54856 NM_001037533.1 Transcript intron_variant - - - - - - rs822480 1:155797432 T ENSESTG00000014369 ENSESTT00000035977 Transcript intron_variant - - - - - - rs822491 1:155823002 C CCDS1121.1 CCDS1121.1 Transcript intron_variant - - - - - - rs822491 1:155823002 C CCDS44242.1 CCDS44242.1 Transcript intron_variant - - - - - - rs822491 1:155823002 C ENSESTG00000014369 ENSESTT00000035933 Transcript intron_variant - - - - - - rs822491 1:155823002 C 54856 NM_032292.4 Transcript intron_variant - - - - - - rs822491 1:155823002 C ENSESTG00000014369 ENSESTT00000035988 Transcript intron_variant - - - - - - rs822491 1:155823002 C 54856 NM_001037533.1 Transcript intron_variant - - - - - - rs822491 1:155823002 C ENSESTG00000014369 ENSESTT00000035977 Transcript intron_variant - - - - - - rs7542692 1:155908205 T - ENSR00000545642 RegulatoryFeature regulatory_region_variant - - - - - - rs7542692 1:155908205 T 339403 NM_181885.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3275 rs7542692 1:155908205 T 22889 NM_014949.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4017 rs7542692 1:155908205 T CCDS1124.1 CCDS1124.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3296 rs7542692 1:155908205 T ENSESTG00000014645 ENSESTT00000036682 Transcript upstream_gene_variant - - - - - - DISTANCE=4043 rs7542692 1:155908205 T CCDS30885.1 CCDS30885.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4041 rs4661216 1:155955076 G ENSESTG00000014634 ENSESTT00000036614 Transcript upstream_gene_variant - - - - - - DISTANCE=1680 rs4661216 1:155955076 G ENSESTG00000014060 ENSESTT00000035135 Transcript downstream_gene_variant - - - - - - DISTANCE=3885 rs4661216 1:155955076 G ENSESTG00000014634 ENSESTT00000036607 Transcript intron_variant - - - - - - rs4661216 1:155955076 G ENSESTG00000014620 ENSESTT00000036581 Transcript intron_variant - - - - - - rs3001784 1:156279210 C CCDS1140.2 CCDS1140.2 Transcript intron_variant - - - - - - rs3001784 1:156279210 C ENSESTG00000014483 ENSESTT00000036390 Transcript downstream_gene_variant - - - - - - DISTANCE=2756 rs3001784 1:156279210 C CCDS30888.1 CCDS30888.1 Transcript intron_variant - - - - - - rs3001784 1:156279210 C 7203 NM_001008800.2 Transcript intron_variant - - - - - - rs3001784 1:156279210 C ENSESTG00000014483 ENSESTT00000036412 Transcript intron_variant - - - - - - rs3001784 1:156279210 C ENSESTG00000014483 ENSESTT00000036350 Transcript intron_variant - - - - - - rs3001784 1:156279210 C 7203 NR_036565.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3001784 1:156279210 C 7203 NM_005998.4 Transcript intron_variant - - - - - - rs3001784 1:156279210 C 7203 NR_036564.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3001784 1:156279210 C ENSESTG00000014483 ENSESTT00000036415 Transcript downstream_gene_variant - - - - - - DISTANCE=2756 rs6662064 1:156376680 G ENSESTG00000014447 ENSESTT00000036223 Transcript intron_variant - - - - - - rs6662064 1:156376680 G ENSESTG00000014447 ENSESTT00000036240 Transcript intron_variant - - - - - - rs6662064 1:156376680 G ENSESTG00000014447 ENSESTT00000036208 Transcript downstream_gene_variant - - - - - - DISTANCE=821 rs6662064 1:156376680 G 10485 NM_006365.1 Transcript intron_variant - - - - - - rs6662064 1:156376680 G ENSESTG00000014447 ENSESTT00000036231 Transcript downstream_gene_variant - - - - - - DISTANCE=839 rs6662064 1:156376680 G CCDS1142.1 CCDS1142.1 Transcript intron_variant - - - - - - rs6662064 1:156376680 G ENSESTG00000014447 ENSESTT00000036236 Transcript downstream_gene_variant - - - - - - DISTANCE=809 rs6662064 1:156376680 G ENSESTG00000014447 ENSESTT00000036206 Transcript intron_variant - - - - - - rs6698766 1:156394886 A 407046 NR_029691.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4665 rs6698766 1:156394886 A ENSESTG00000014447 ENSESTT00000036223 Transcript upstream_gene_variant - - - - - - DISTANCE=3369 rs6698766 1:156394886 A ENSESTG00000014447 ENSESTT00000036240 Transcript upstream_gene_variant - - - - - - DISTANCE=4805 rs6698766 1:156394886 A ENSESTG00000014447 ENSESTT00000036208 Transcript intron_variant - - - - - - rs6698766 1:156394886 A 10485 NM_006365.1 Transcript intron_variant - - - - - - rs6698766 1:156394886 A ENSESTG00000014447 ENSESTT00000036231 Transcript upstream_gene_variant - - - - - - DISTANCE=4773 rs6698766 1:156394886 A ENSESTG00000014447 ENSESTT00000036193 Transcript intron_variant - - - - - - rs6698766 1:156394886 A ENSESTG00000014447 ENSESTT00000036236 Transcript upstream_gene_variant - - - - - - DISTANCE=4776 rs6698766 1:156394886 A ENSESTG00000014447 ENSESTT00000036206 Transcript intron_variant - - - - - - rs6698766 1:156394886 A ENSESTG00000014447 ENSESTT00000036212 Transcript intron_variant - - - - - - rs1171661 1:156420122 A ENSESTG00000014447 ENSESTT00000036193 Transcript intron_variant - - - - - - rs1171562 1:156456297 T ENSESTG00000014424 ENSESTT00000036119 Transcript intron_variant - - - - - - rs1171562 1:156456297 T ENSESTG00000014424 ENSESTT00000036114 Transcript intron_variant - - - - - - rs1171562 1:156456297 T ENSESTG00000014424 ENSESTT00000036122 Transcript intron_variant - - - - - - rs1171562 1:156456297 T CCDS1143.1 CCDS1143.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3213 rs1171562 1:156456297 T 4209 NM_005920.2 Transcript intron_variant - - - - - - rs2181936 1:157239228 C - - - intergenic_variant - - - - - - rs2777818 1:157977612 G ENSESTG00000011788 ENSESTT00000029582 Transcript intron_variant - - - - - - rs2777818 1:157977612 G ENSESTG00000011788 ENSESTT00000029568 Transcript intron_variant - - - - - - rs2777818 1:157977612 G CCDS1172.2 CCDS1172.2 Transcript intron_variant - - - - - - rs2777818 1:157977612 G 55243 NM_018240.5 Transcript intron_variant - - - - - - rs6693829 1:158079972 T - - - intergenic_variant - - - - - - rs78804192 1:158120478 C - - - intergenic_variant - - - - - - rs1324658 1:158143772 A ENSESTG00000011808 ENSESTT00000029626 Transcript upstream_gene_variant - - - - - - DISTANCE=4056 rs1324658 1:158143772 A ENSESTG00000011808 ENSESTT00000029635 Transcript upstream_gene_variant - - - - - - DISTANCE=4062 rs857796 1:158801566 A 4332 NM_002432.1 Transcript intron_variant - - - - - - rs857796 1:158801566 A ENSESTG00000022371 ENSESTT00000056518 Transcript intron_variant - - - - - - rs857796 1:158801566 A ENSESTG00000022371 ENSESTT00000056476 Transcript intron_variant - - - - - - rs857796 1:158801566 A ENSESTG00000022371 ENSESTT00000056500 Transcript intron_variant - - - - - - rs1231165 1:158875814 A - - - intergenic_variant - - - - - - rs863001 1:159174824 C 57863 NM_021189.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1892 rs863001 1:159174824 C ENSESTG00000022583 ENSESTT00000057156 Transcript downstream_gene_variant - - - - - - DISTANCE=3886 rs863001 1:159174824 C CCDS44252.1 CCDS44252.1 Transcript upstream_gene_variant - - - - - - DISTANCE=400 rs863001 1:159174824 C 2532 NM_001122951.2 Transcript upstream_gene_variant - - - - - - DISTANCE=225 rs863001 1:159174824 C 57863 NM_001127173.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1892 rs863001 1:159174824 C ENSESTG00000022583 ENSESTT00000057212 Transcript downstream_gene_variant - - - - - - DISTANCE=3886 rs863001 1:159174824 C CCDS1182.1 CCDS1182.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4112 rs863001 1:159174824 C 100131825 NR_037870.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2612 rs863001 1:159174824 C CCDS44251.1 CCDS44251.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4112 rs863001 1:159174824 C CCDS1183.1 CCDS1183.1 Transcript intron_variant - - - - - - rs863001 1:159174824 C 2532 NM_002036.3 Transcript intron_variant - - - - - - rs3003312 1:159794032 C ENSESTG00000002814 ENSESTT00000006985 Transcript upstream_gene_variant - - - - - - DISTANCE=2630 rs3003312 1:159794032 C ENSESTG00000002814 ENSESTT00000006983 Transcript upstream_gene_variant - - - - - - DISTANCE=2447 rs3003312 1:159794032 C 56833 NM_020125.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2447 rs3003312 1:159794032 C CCDS1188.1 CCDS1188.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2657 rs2820563 1:159981824 C - - - intergenic_variant - - - - - - rs9659413 1:159987072 T - - - intergenic_variant - - - - - - rs2854246 1:160090674 C CCDS1196.1 CCDS1196.1 Transcript intron_variant - - - - - - rs2854246 1:160090674 C ENSESTG00000002849 ENSESTT00000007098 Transcript intron_variant - - - - - - rs2854246 1:160090674 C 477 NM_000702.3 Transcript intron_variant - - - - - - rs947494 1:160232806 G - ENSR00001525230 RegulatoryFeature regulatory_region_variant - - - - - - rs947494 1:160232806 G 50717 NR_028105.1 Transcript upstream_gene_variant - - - - - - DISTANCE=488 rs947494 1:160232806 G ENSESTG00000003198 ENSESTT00000007978 Transcript upstream_gene_variant - - - - - - DISTANCE=551 rs947494 1:160232806 G 50717 NM_015726.3 Transcript upstream_gene_variant - - - - - - DISTANCE=456 rs947494 1:160232806 G ENSESTG00000003198 ENSESTT00000008022 Transcript upstream_gene_variant - - - - - - DISTANCE=2451 rs947494 1:160232806 G 50717 NR_028104.1 Transcript upstream_gene_variant - - - - - - DISTANCE=488 rs947494 1:160232806 G 50717 NR_028103.1 Transcript upstream_gene_variant - - - - - - DISTANCE=488 rs947494 1:160232806 G ENSESTG00000002979 ENSESTT00000007404 Transcript downstream_gene_variant - - - - - - DISTANCE=296 rs947494 1:160232806 G ENSESTG00000003198 ENSESTT00000007979 Transcript upstream_gene_variant - - - - - - DISTANCE=1355 rs947494 1:160232806 G 50717 NR_028106.1 Transcript upstream_gene_variant - - - - - - DISTANCE=529 rs7549221 1:160655583 G CCDS1208.1 CCDS1208.1 Transcript intron_variant - - - - - - rs7549221 1:160655583 G ENSESTG00000029718 ENSESTT00000074816 Transcript intron_variant - - - - - - rs7549221 1:160655583 G 962 NM_001778.3 Transcript intron_variant - - - - - - rs7549221 1:160655583 G ENSESTG00000029718 ENSESTT00000074828 Transcript intron_variant - - - - - - rs7549221 1:160655583 G 962 NM_001256030.1 Transcript intron_variant - - - - - - rs7549221 1:160655583 G ENSESTG00000027736 ENSESTT00000069808 Transcript downstream_gene_variant - - - - - - DISTANCE=1885 rs7549403 1:160655950 G CCDS1208.1 CCDS1208.1 Transcript intron_variant - - - - - - rs7549403 1:160655950 G ENSESTG00000029718 ENSESTT00000074816 Transcript intron_variant - - - - - - rs7549403 1:160655950 G 962 NM_001778.3 Transcript intron_variant - - - - - - rs7549403 1:160655950 G ENSESTG00000029718 ENSESTT00000074828 Transcript intron_variant - - - - - - rs7549403 1:160655950 G 962 NM_001256030.1 Transcript intron_variant - - - - - - rs7549403 1:160655950 G ENSESTG00000027736 ENSESTT00000069808 Transcript downstream_gene_variant - - - - - - DISTANCE=2252 rs503721 1:160750931 G - - - intergenic_variant - - - - - - rs2769586 1:160761774 C CCDS30916.1 CCDS30916.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4204 rs2769586 1:160761774 C 4063 NM_001261457.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4090 rs2769586 1:160761774 C CCDS30917.1 CCDS30917.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4204 rs2769586 1:160761774 C ENSESTG00000027806 ENSESTT00000070027 Transcript upstream_gene_variant - - - - - - DISTANCE=4090 rs2769586 1:160761774 C 4063 NM_001033667.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4090 rs2769586 1:160761774 C ENSESTG00000027806 ENSESTT00000070005 Transcript upstream_gene_variant - - - - - - DISTANCE=4090 rs2769586 1:160761774 C ENSESTG00000027806 ENSESTT00000070015 Transcript upstream_gene_variant - - - - - - DISTANCE=4090 rs2769586 1:160761774 C 4063 NM_002348.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4090 rs2769586 1:160761774 C 4063 NM_001261456.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4090 rs525677 1:160773143 G CCDS30916.1 CCDS30916.1 Transcript intron_variant - - - - - - rs525677 1:160773143 G 4063 NM_001261457.1 Transcript intron_variant - - - - - - rs525677 1:160773143 G CCDS30917.1 CCDS30917.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1436 rs525677 1:160773143 G ENSESTG00000027806 ENSESTT00000070027 Transcript downstream_gene_variant - - - - - - DISTANCE=1296 rs525677 1:160773143 G 4063 NM_001033667.2 Transcript downstream_gene_variant - - - - - - DISTANCE=607 rs525677 1:160773143 G ENSESTG00000027806 ENSESTT00000070005 Transcript intron_variant - - - - - - rs525677 1:160773143 G ENSESTG00000027806 ENSESTT00000070015 Transcript intron_variant - - - - - - rs525677 1:160773143 G 4063 NM_002348.3 Transcript intron_variant - - - - - - rs525677 1:160773143 G 4063 NM_001261456.1 Transcript intron_variant - - - - - - rs481243 1:160777098 C CCDS30916.1 CCDS30916.1 Transcript intron_variant - - - - - - rs481243 1:160777098 C 4063 NM_001033667.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4562 rs481243 1:160777098 C ENSESTG00000027806 ENSESTT00000070005 Transcript intron_variant - - - - - - rs481243 1:160777098 C 4063 NM_001261457.1 Transcript intron_variant - - - - - - rs481243 1:160777098 C 4063 NM_002348.3 Transcript intron_variant - - - - - - rs481243 1:160777098 C ENSESTG00000027806 ENSESTT00000070015 Transcript intron_variant - - - - - - rs481243 1:160777098 C 4063 NM_001261456.1 Transcript intron_variant - - - - - - rs489910 1:160812576 C 51744 NM_001166664.1 Transcript intron_variant - - - - - - rs489910 1:160812576 C CCDS53398.1 CCDS53398.1 Transcript intron_variant - - - - - - rs489910 1:160812576 C 51744 NM_001166663.1 Transcript intron_variant - - - - - - rs489910 1:160812576 C ENSESTG00000029664 ENSESTT00000074693 Transcript intron_variant - - - - - - rs489910 1:160812576 C ENSESTG00000029664 ENSESTT00000074609 Transcript intron_variant - - - - - - rs489910 1:160812576 C CCDS1210.1 CCDS1210.1 Transcript intron_variant - - - - - - rs489910 1:160812576 C ENSESTG00000029664 ENSESTT00000074641 Transcript intron_variant - - - - - - rs489910 1:160812576 C 51744 NM_016382.3 Transcript intron_variant - - - - - - rs489910 1:160812576 C CCDS53399.1 CCDS53399.1 Transcript intron_variant - - - - - - rs489910 1:160812576 C ENSESTG00000029664 ENSESTT00000074720 Transcript upstream_gene_variant - - - - - - DISTANCE=3621 rs538432 1:160814315 C 51744 NM_001166664.1 Transcript intron_variant - - - - - - rs538432 1:160814315 C CCDS53398.1 CCDS53398.1 Transcript intron_variant - - - - - - rs538432 1:160814315 C 51744 NM_001166663.1 Transcript intron_variant - - - - - - rs538432 1:160814315 C ENSESTG00000029664 ENSESTT00000074693 Transcript intron_variant - - - - - - rs538432 1:160814315 C ENSESTG00000029664 ENSESTT00000074609 Transcript intron_variant - - - - - - rs538432 1:160814315 C CCDS1210.1 CCDS1210.1 Transcript intron_variant - - - - - - rs538432 1:160814315 C ENSESTG00000029664 ENSESTT00000074641 Transcript intron_variant - - - - - - rs538432 1:160814315 C 51744 NM_016382.3 Transcript intron_variant - - - - - - rs538432 1:160814315 C CCDS53399.1 CCDS53399.1 Transcript intron_variant - - - - - - rs6674383 1:161276434 G - ENSR00000080585 RegulatoryFeature regulatory_region_variant - - - - - - rs6674383 1:161276434 G ENSESTG00000028883 ENSESTT00000072827 Transcript intron_variant - - - - - - rs6674383 1:161276434 G 4359 NM_000530.6 Transcript intron_variant - - - - - - rs6674383 1:161276434 G CCDS1229.2 CCDS1229.2 Transcript intron_variant - - - - - - rs6674383 1:161276434 G ENSESTG00000028883 ENSESTT00000072808 Transcript intron_variant - - - - - - rs7540674 1:162114174 A CCDS53421.1 CCDS53421.1 Transcript intron_variant - - - - - - rs7540674 1:162114174 A CCDS1237.1 CCDS1237.1 Transcript intron_variant - - - - - - rs7540674 1:162114174 A 9722 NM_001164757.1 Transcript intron_variant - - - - - - rs7540674 1:162114174 A 9722 NM_014697.2 Transcript intron_variant - - - - - - rs4385683 1:162182524 G CCDS53421.1 CCDS53421.1 Transcript intron_variant - - - - - - rs4385683 1:162182524 G CCDS1237.1 CCDS1237.1 Transcript intron_variant - - - - - - rs4385683 1:162182524 G 9722 NM_001164757.1 Transcript intron_variant - - - - - - rs4385683 1:162182524 G 9722 NM_014697.2 Transcript intron_variant - - - - - - rs2791145 1:163568943 T - - - intergenic_variant - - - - - - rs2247668 1:163650332 A - - - intergenic_variant - - - - - - rs1289006 1:163663216 G - - - intergenic_variant - - - - - - rs6426863 1:164227219 C - - - intergenic_variant - - - - - - rs1686177 1:164678896 G CCDS55654.1 CCDS55654.1 Transcript intron_variant - - - - - - rs1686177 1:164678896 G 5087 NM_001204961.1 Transcript intron_variant - - - - - - rs1686177 1:164678896 G CCDS1246.1 CCDS1246.1 Transcript intron_variant - - - - - - rs1686177 1:164678896 G ENSESTG00000017533 ENSESTT00000044160 Transcript intron_variant - - - - - - rs1686177 1:164678896 G ENSESTG00000017533 ENSESTT00000044222 Transcript intron_variant - - - - - - rs1686177 1:164678896 G CCDS55653.1 CCDS55653.1 Transcript intron_variant - - - - - - rs1686177 1:164678896 G ENSESTG00000017533 ENSESTT00000044184 Transcript intron_variant - - - - - - rs1686177 1:164678896 G 5087 NM_001204963.1 Transcript intron_variant - - - - - - rs1686177 1:164678896 G 5087 NM_002585.3 Transcript intron_variant - - - - - - rs1686177 1:164678896 G ENSESTG00000017533 ENSESTT00000044205 Transcript intron_variant - - - - - - rs1686177 1:164678896 G ENSESTG00000017533 ENSESTT00000044200 Transcript intron_variant - - - - - - rs1686177 1:164678896 G ENSESTG00000017533 ENSESTT00000044194 Transcript intron_variant - - - - - - rs1686177 1:164678896 G ENSESTG00000017533 ENSESTT00000044203 Transcript intron_variant - - - - - - rs1213268 1:164782266 G - ENSR00000546845 RegulatoryFeature regulatory_region_variant - - - - - - rs1213268 1:164782266 G 5087 NM_001204961.1 Transcript intron_variant - - - - - - rs1213268 1:164782266 G CCDS1246.1 CCDS1246.1 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044243 Transcript downstream_gene_variant - - - - - - DISTANCE=875 rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044160 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044222 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044239 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044252 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044184 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044268 Transcript intron_variant - - - - - - rs1213268 1:164782266 G 5087 NM_001204963.1 Transcript intron_variant - - - - - - rs1213268 1:164782266 G 5087 NM_002585.3 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044271 Transcript downstream_gene_variant - - - - - - DISTANCE=875 rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044205 Transcript downstream_gene_variant - - - - - - DISTANCE=875 rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044267 Transcript intron_variant - - - - - - rs1213268 1:164782266 G CCDS55654.1 CCDS55654.1 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044234 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044259 Transcript downstream_gene_variant - - - - - - DISTANCE=875 rs1213268 1:164782266 G CCDS55653.1 CCDS55653.1 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044257 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044200 Transcript intron_variant - - - - - - rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044194 Transcript downstream_gene_variant - - - - - - DISTANCE=875 rs1213268 1:164782266 G ENSESTG00000017533 ENSESTT00000044203 Transcript intron_variant - - - - - - rs1538488 1:164789444 G 5087 NM_001204961.1 Transcript intron_variant - - - - - - rs1538488 1:164789444 G CCDS1246.1 CCDS1246.1 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044160 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044222 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044239 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044252 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044184 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044268 Transcript intron_variant - - - - - - rs1538488 1:164789444 G 5087 NM_001204963.1 Transcript intron_variant - - - - - - rs1538488 1:164789444 G 5087 NM_002585.3 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044267 Transcript intron_variant - - - - - - rs1538488 1:164789444 G CCDS55654.1 CCDS55654.1 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044234 Transcript intron_variant - - - - - - rs1538488 1:164789444 G CCDS55653.1 CCDS55653.1 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044200 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044257 Transcript intron_variant - - - - - - rs1538488 1:164789444 G ENSESTG00000017533 ENSESTT00000044203 Transcript intron_variant - - - - - - rs1234517 1:164804245 A 5087 NM_001204961.1 Transcript intron_variant - - - - - - rs1234517 1:164804245 A CCDS1246.1 CCDS1246.1 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044160 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044222 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044239 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044252 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044184 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044268 Transcript intron_variant - - - - - - rs1234517 1:164804245 A 5087 NM_001204963.1 Transcript intron_variant - - - - - - rs1234517 1:164804245 A 5087 NM_002585.3 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044267 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044234 Transcript intron_variant - - - - - - rs1234517 1:164804245 A CCDS55653.1 CCDS55653.1 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044200 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044257 Transcript intron_variant - - - - - - rs1234517 1:164804245 A ENSESTG00000017533 ENSESTT00000044203 Transcript intron_variant - - - - - - rs2055119 1:165109922 T - - - intergenic_variant - - - - - - rs7512132 1:165223037 G - ENSR00001525558 RegulatoryFeature regulatory_region_variant - - - - - - rs7512132 1:165223037 G 4009 NM_177398.3 Transcript intron_variant - - - - - - rs7512132 1:165223037 G 4009 NM_001174069.1 Transcript intron_variant - - - - - - rs7512132 1:165223037 G ENSESTG00000017692 ENSESTT00000044592 Transcript upstream_gene_variant - - - - - - DISTANCE=4158 rs7512132 1:165223037 G CCDS1247.1 CCDS1247.1 Transcript intron_variant - - - - - - rs7512132 1:165223037 G ENSESTG00000017692 ENSESTT00000044578 Transcript intron_variant - - - - - - rs10732282 1:165248901 G 4009 NM_177398.3 Transcript intron_variant - - - - - - rs10732282 1:165248901 G 4009 NM_001174069.1 Transcript intron_variant - - - - - - rs10732282 1:165248901 G CCDS1247.1 CCDS1247.1 Transcript intron_variant - - - - - - rs10732282 1:165248901 G ENSESTG00000017692 ENSESTT00000044578 Transcript intron_variant - - - - - - rs6679722 1:165262619 T 4009 NM_177398.3 Transcript intron_variant - - - - - - rs6679722 1:165262619 T 4009 NM_001174069.1 Transcript intron_variant - - - - - - rs6679722 1:165262619 T CCDS1247.1 CCDS1247.1 Transcript intron_variant - - - - - - rs6679722 1:165262619 T ENSESTG00000017692 ENSESTT00000044578 Transcript intron_variant - - - - - - rs283699 1:165374434 A CCDS1248.1 CCDS1248.1 Transcript intron_variant - - - - - - rs283699 1:165374434 A 6258 NM_001256571.1 Transcript intron_variant - - - - - - rs283699 1:165374434 A 6258 NM_006917.4 Transcript intron_variant - - - - - - rs283699 1:165374434 A 6258 NM_001256570.1 Transcript intron_variant - - - - - - rs157882 1:165402146 C CCDS1248.1 CCDS1248.1 Transcript intron_variant - - - - - - rs157882 1:165402146 C 6258 NM_006917.4 Transcript intron_variant - - - - - - rs157882 1:165402146 C 6258 NR_033824.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4019 rs157882 1:165402146 C ENSESTG00000017644 ENSESTT00000044549 Transcript intron_variant - - - - - - rs157882 1:165402146 C 6258 NM_001256570.1 Transcript intron_variant - - - - - - rs188195 1:165409982 G CCDS1248.1 CCDS1248.1 Transcript intron_variant - - - - - - rs188195 1:165409982 G 6258 NM_006917.4 Transcript intron_variant - - - - - - rs188195 1:165409982 G 6258 NR_033824.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs188195 1:165409982 G ENSESTG00000017644 ENSESTT00000044549 Transcript intron_variant - - - - - - rs188195 1:165409982 G 6258 NM_001256570.1 Transcript intron_variant - - - - - - rs157888 1:165413282 G - ENSR00000167204 RegulatoryFeature regulatory_region_variant - - - - - - rs157888 1:165413282 G CCDS1248.1 CCDS1248.1 Transcript intron_variant - - - - - - rs157888 1:165413282 G 6258 NM_006917.4 Transcript intron_variant - - - - - - rs157888 1:165413282 G 6258 NR_033824.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs157888 1:165413282 G ENSESTG00000017644 ENSESTT00000044549 Transcript intron_variant - - - - - - rs157888 1:165413282 G 6258 NM_001256570.1 Transcript intron_variant - - - - - - rs190798 1:165435587 C - - - intergenic_variant - - - - - - rs927842 1:165470830 T 400794 NR_026744.1 Transcript non_coding_exon_variant,nc_transcript_variant 1057 - - - - - rs1213750 1:165541062 T 400794 NR_026744.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4431823 1:165824040 A CCDS1252.1 CCDS1252.1 Transcript intron_variant - - - - - - rs4431823 1:165824040 A ENSESTG00000031035 ENSESTT00000078093 Transcript intron_variant - - - - - - rs4431823 1:165824040 A ENSESTG00000030973 ENSESTT00000078047 Transcript intron_variant - - - - - - rs4431823 1:165824040 A 7371 NM_012474.4 Transcript intron_variant - - - - - - rs6682243 1:165828536 C CCDS1252.1 CCDS1252.1 Transcript intron_variant - - - - - - rs6682243 1:165828536 C ENSESTG00000031035 ENSESTT00000078093 Transcript intron_variant - - - - - - rs6682243 1:165828536 C ENSESTG00000030973 ENSESTT00000078047 Transcript intron_variant - - - - - - rs6682243 1:165828536 C 7371 NM_012474.4 Transcript intron_variant - - - - - - rs477033 1:165859630 G CCDS1252.1 CCDS1252.1 Transcript intron_variant - - - - - - rs477033 1:165859630 G ENSESTG00000031035 ENSESTT00000078093 Transcript intron_variant - - - - - - rs477033 1:165859630 G ENSESTG00000030973 ENSESTT00000078047 Transcript intron_variant - - - - - - rs477033 1:165859630 G 7371 NM_012474.4 Transcript intron_variant - - - - - - rs546390 1:165874875 A CCDS1252.1 CCDS1252.1 Transcript intron_variant - - - - - - rs546390 1:165874875 A ENSESTG00000030973 ENSESTT00000078080 Transcript intron_variant - - - - - - rs546390 1:165874875 A 100500832 NR_037431.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2283 rs546390 1:165874875 A ENSESTG00000030973 ENSESTT00000078047 Transcript intron_variant - - - - - - rs546390 1:165874875 A 7371 NM_012474.4 Transcript intron_variant - - - - - - rs546390 1:165874875 A ENSESTG00000030973 ENSESTT00000078071 Transcript intron_variant - - - - - - rs1768901 1:165895012 A ENSESTG00000031041 ENSESTT00000078114 Transcript intron_variant - - - - - - rs10800182 1:166051400 A CCDS30931.1 CCDS30931.1 Transcript intron_variant - - - - - - rs10800182 1:166051400 A ENSESTG00000031054 ENSESTT00000078159 Transcript intron_variant - - - - - - rs10800182 1:166051400 A ENSESTG00000031041 ENSESTT00000078114 Transcript intron_variant - - - - - - rs10800182 1:166051400 A 149297 NM_001017961.3 Transcript intron_variant - - - - - - rs6687565 1:166060654 T CCDS30931.1 CCDS30931.1 Transcript intron_variant - - - - - - rs6687565 1:166060654 T ENSESTG00000031054 ENSESTT00000078159 Transcript intron_variant - - - - - - rs6687565 1:166060654 T ENSESTG00000031041 ENSESTT00000078114 Transcript downstream_gene_variant - - - - - - DISTANCE=3858 rs6687565 1:166060654 T 149297 NM_001017961.3 Transcript intron_variant - - - - - - rs4656478 1:166098581 G CCDS30931.1 CCDS30931.1 Transcript intron_variant - - - - - - rs4656478 1:166098581 G ENSESTG00000031054 ENSESTT00000078159 Transcript intron_variant - - - - - - rs4656478 1:166098581 G 149297 NM_001017961.3 Transcript intron_variant - - - - - - rs6675688 1:166099642 G CCDS30931.1 CCDS30931.1 Transcript intron_variant - - - - - - rs6675688 1:166099642 G ENSESTG00000031054 ENSESTT00000078159 Transcript intron_variant - - - - - - rs6675688 1:166099642 G 149297 NM_001017961.3 Transcript intron_variant - - - - - - rs2310779 1:166202097 C - - - intergenic_variant - - - - - - rs2163631 1:166256086 C - - - intergenic_variant - - - - - - rs6660302 1:166486277 G - - - intergenic_variant - - - - - - rs198983 1:166521924 C - - - intergenic_variant - - - - - - rs704857 1:166735502 T - - - intergenic_variant - - - - - - rs4657635 1:167104774 G ENSESTG00000008597 ENSESTT00000021620 Transcript intron_variant - - - - - - rs2860509 1:167220665 A ENSESTG00000008449 ENSESTT00000021360 Transcript intron_variant - - - - - - rs2860509 1:167220665 A 5451 NM_002697.3 Transcript intron_variant - - - - - - rs2860509 1:167220665 A 5451 NM_001198786.1 Transcript intron_variant - - - - - - rs2860509 1:167220665 A 5451 NR_037163.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2860509 1:167220665 A ENSESTG00000008449 ENSESTT00000021364 Transcript intron_variant - - - - - - rs2860509 1:167220665 A CCDS1259.2 CCDS1259.2 Transcript intron_variant - - - - - - rs2860509 1:167220665 A CCDS55655.1 CCDS55655.1 Transcript intron_variant - - - - - - rs2949667 1:167397177 G 5451 NM_001198786.1 Transcript downstream_gene_variant - - - - - - DISTANCE=595 rs2949667 1:167397177 G 5451 NR_037163.1 Transcript downstream_gene_variant - - - - - - DISTANCE=595 rs2949667 1:167397177 G CCDS1260.1 CCDS1260.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3741 rs2949667 1:167397177 G 919 NM_000734.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2700 rs2949667 1:167397177 G 5451 NM_001198783.1 Transcript downstream_gene_variant - - - - - - DISTANCE=595 rs2949667 1:167397177 G ENSESTG00000008552 ENSESTT00000021554 Transcript downstream_gene_variant - - - - - - DISTANCE=3666 rs2949667 1:167397177 G 5451 NM_002697.3 Transcript downstream_gene_variant - - - - - - DISTANCE=595 rs2949667 1:167397177 G CCDS1261.1 CCDS1261.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3741 rs2949667 1:167397177 G 919 NM_198053.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2700 rs2995092 1:167435392 C ENSESTG00000008552 ENSESTT00000021582 Transcript intron_variant - - - - - - rs2995092 1:167435392 C ENSESTG00000008552 ENSESTT00000021564 Transcript intron_variant - - - - - - rs2995092 1:167435392 C CCDS1260.1 CCDS1260.1 Transcript intron_variant - - - - - - rs2995092 1:167435392 C 919 NM_000734.3 Transcript intron_variant - - - - - - rs2995092 1:167435392 C ENSESTG00000008552 ENSESTT00000021587 Transcript intron_variant - - - - - - rs2995092 1:167435392 C ENSESTG00000008552 ENSESTT00000021554 Transcript intron_variant - - - - - - rs2995092 1:167435392 C CCDS1261.1 CCDS1261.1 Transcript intron_variant - - - - - - rs2995092 1:167435392 C ENSESTG00000008552 ENSESTT00000021556 Transcript intron_variant - - - - - - rs2995092 1:167435392 C 919 NM_198053.2 Transcript intron_variant - - - - - - rs2995092 1:167435392 C ENSESTG00000008552 ENSESTT00000021568 Transcript intron_variant - - - - - - rs704858 1:167495518 C ENSESTG00000023064 ENSESTT00000058201 Transcript upstream_gene_variant - - - - - - DISTANCE=3723 rs761077 1:167618895 A - ENSR00001525689 RegulatoryFeature regulatory_region_variant - - - - - - rs761077 1:167618895 A ENSESTG00000023075 ENSESTT00000058276 Transcript intron_variant - - - - - - rs761077 1:167618895 A ENSESTG00000023075 ENSESTT00000058237 Transcript intron_variant - - - - - - rs761077 1:167618895 A CCDS1263.1 CCDS1263.1 Transcript intron_variant - - - - - - rs761077 1:167618895 A ENSESTG00000023075 ENSESTT00000058319 Transcript intron_variant - - - - - - rs761077 1:167618895 A 92241 NM_052862.3 Transcript intron_variant - - - - - - rs1229296 1:167700645 G ENSESTG00000023133 ENSESTT00000058444 Transcript intron_variant - - - - - - rs1229296 1:167700645 G CCDS44273.1 CCDS44273.1 Transcript intron_variant - - - - - - rs1229296 1:167700645 G ENSESTG00000023133 ENSESTT00000058542 Transcript intron_variant - - - - - - rs1229296 1:167700645 G ENSESTG00000023133 ENSESTT00000058474 Transcript intron_variant - - - - - - rs1229296 1:167700645 G CCDS1264.1 CCDS1264.1 Transcript intron_variant - - - - - - rs1229296 1:167700645 G 9019 NM_001146191.1 Transcript intron_variant - - - - - - rs1229296 1:167700645 G 9019 NM_024569.4 Transcript intron_variant - - - - - - rs1229296 1:167700645 G 9019 NM_003953.5 Transcript intron_variant - - - - - - rs1229296 1:167700645 G CCDS53425.1 CCDS53425.1 Transcript intron_variant - - - - - - rs2051657 1:167810706 T CCDS53426.1 CCDS53426.1 Transcript intron_variant - - - - - - rs2051657 1:167810706 T 55811 NM_018417.4 Transcript intron_variant - - - - - - rs2051657 1:167810706 T CCDS1265.1 CCDS1265.1 Transcript intron_variant - - - - - - rs2051657 1:167810706 T 55811 NM_001167749.1 Transcript intron_variant - - - - - - rs189958 1:167820588 C CCDS53426.1 CCDS53426.1 Transcript intron_variant - - - - - - rs189958 1:167820588 C 55811 NM_018417.4 Transcript intron_variant - - - - - - rs189958 1:167820588 C CCDS1265.1 CCDS1265.1 Transcript intron_variant - - - - - - rs189958 1:167820588 C 55811 NM_001167749.1 Transcript intron_variant - - - - - - rs1235334 1:167820680 C CCDS53426.1 CCDS53426.1 Transcript intron_variant - - - - - - rs1235334 1:167820680 C 55811 NM_018417.4 Transcript intron_variant - - - - - - rs1235334 1:167820680 C CCDS1265.1 CCDS1265.1 Transcript intron_variant - - - - - - rs1235334 1:167820680 C 55811 NM_001167749.1 Transcript intron_variant - - - - - - rs203774 1:167871565 C CCDS53426.1 CCDS53426.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2722 rs203774 1:167871565 C ENSESTG00000023863 ENSESTT00000060254 Transcript intron_variant - - - - - - rs203774 1:167871565 C ENSESTG00000023863 ENSESTT00000060176 Transcript intron_variant - - - - - - rs203774 1:167871565 C 55811 NM_018417.4 Transcript intron_variant - - - - - - rs203774 1:167871565 C CCDS1265.1 CCDS1265.1 Transcript intron_variant - - - - - - rs203774 1:167871565 C 55811 NM_001167749.1 Transcript intron_variant - - - - - - rs203774 1:167871565 C ENSESTG00000023863 ENSESTT00000060202 Transcript intron_variant - - - - - - rs203788 1:167906239 C - ENSR00000286976 RegulatoryFeature regulatory_region_variant - - - - - - rs203788 1:167906239 C CCDS55658.1 CCDS55658.1 Transcript synonymous_variant 90 90 30 R cgA/cgC - rs203788 1:167906239 C 55827 NM_001198957.1 Transcript synonymous_variant 443 90 30 R cgA/cgC - rs203788 1:167906239 C CCDS1267.2 CCDS1267.2 Transcript synonymous_variant 90 90 30 R cgA/cgC - rs203788 1:167906239 C ENSESTG00000023218 ENSESTT00000059097 Transcript upstream_gene_variant - - - - - - DISTANCE=604 rs203788 1:167906239 C ENSESTG00000023218 ENSESTT00000058956 Transcript intron_variant - - - - - - rs203788 1:167906239 C 25874 NR_026550.2 Transcript upstream_gene_variant - - - - - - DISTANCE=800 rs203788 1:167906239 C 55827 NM_018442.3 Transcript synonymous_variant 443 90 30 R cgA/cgC - rs203788 1:167906239 C 55827 NM_001017977.2 Transcript synonymous_variant 443 90 30 R cgA/cgC - rs203788 1:167906239 C CCDS30933.1 CCDS30933.1 Transcript synonymous_variant 90 90 30 R cgA/cgC - rs203788 1:167906239 C ENSESTG00000023218 ENSESTT00000059084 Transcript intron_variant - - - - - - rs203788 1:167906239 C CCDS1266.1 CCDS1266.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1160 rs203788 1:167906239 C ENSESTG00000023804 ENSESTT00000060077 Transcript 5_prime_UTR_variant 73 - - - - - rs203788 1:167906239 C ENSESTG00000023804 ENSESTT00000060096 Transcript 5_prime_UTR_variant 40 - - - - - rs203788 1:167906239 C ENSESTG00000023804 ENSESTT00000060134 Transcript upstream_gene_variant - - - - - - DISTANCE=993 rs203788 1:167906239 C CCDS55657.1 CCDS55657.1 Transcript synonymous_variant 90 90 30 R cgA/cgC - rs203788 1:167906239 C 25874 NM_001143674.2 Transcript 5_prime_UTR_variant 69 - - - - - rs203788 1:167906239 C ENSESTG00000023804 ENSESTT00000060089 Transcript splice_region_variant,intron_variant - - - - - - rs203788 1:167906239 C ENSESTG00000023804 ENSESTT00000060121 Transcript upstream_gene_variant - - - - - - DISTANCE=859 rs203788 1:167906239 C 55827 NM_001198956.1 Transcript synonymous_variant 443 90 30 R cgA/cgC - rs203788 1:167906239 C 25874 NM_015415.3 Transcript splice_region_variant,intron_variant - - - - - - rs203788 1:167906239 C ENSESTG00000023218 ENSESTT00000059089 Transcript upstream_gene_variant - - - - - - DISTANCE=604 rs6697694 1:168194145 T - ENSR00001525736 RegulatoryFeature regulatory_region_variant - - - - - - rs6697694 1:168194145 T ENSESTG00000023608 ENSESTT00000059545 Transcript upstream_gene_variant - - - - - - DISTANCE=1097 rs6697694 1:168194145 T ENSESTG00000023608 ENSESTT00000059526 Transcript upstream_gene_variant - - - - - - DISTANCE=1039 rs6697694 1:168194145 T 375035 NM_199344.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1110 rs6697694 1:168194145 T ENSESTG00000023608 ENSESTT00000059689 Transcript upstream_gene_variant - - - - - - DISTANCE=1120 rs6697694 1:168194145 T CCDS1271.1 CCDS1271.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1173 rs6697694 1:168194145 T ENSESTG00000023608 ENSESTT00000059561 Transcript upstream_gene_variant - - - - - - DISTANCE=1118 rs6697694 1:168194145 T ENSESTG00000023608 ENSESTT00000059733 Transcript upstream_gene_variant - - - - - - DISTANCE=1121 rs2418473 1:168233512 G ENSESTG00000023608 ENSESTT00000059545 Transcript intron_variant - - - - - - rs501409 1:168684546 T CCDS1275.1 CCDS1275.1 Transcript intron_variant - - - - - - rs501409 1:168684546 T ENSESTG00000004943 ENSESTT00000012576 Transcript intron_variant - - - - - - rs501409 1:168684546 T 1805 NM_001937.4 Transcript intron_variant - - - - - - rs1885556 1:168856597 G ENSESTG00000004939 ENSESTT00000012557 Transcript intron_variant - - - - - - rs1208136 1:169420061 T ENSESTG00000010152 ENSESTT00000025404 Transcript intron_variant - - - - - - rs7532184 1:169592914 A ENSESTG00000025548 ENSESTT00000064475 Transcript intron_variant - - - - - - rs7532184 1:169592914 A 6403 NM_003005.3 Transcript intron_variant - - - - - - rs7532184 1:169592914 A CCDS1282.1 CCDS1282.1 Transcript intron_variant - - - - - - rs2474699 1:169954737 T ENSESTG00000024822 ENSESTT00000063084 Transcript intron_variant - - - - - - rs2474699 1:169954737 T 22920 NM_001204514.1 Transcript intron_variant - - - - - - rs2474699 1:169954737 T CCDS1288.1 CCDS1288.1 Transcript intron_variant - - - - - - rs2474699 1:169954737 T CCDS55660.1 CCDS55660.1 Transcript intron_variant - - - - - - rs2474699 1:169954737 T 22920 NM_001204516.1 Transcript intron_variant - - - - - - rs2474699 1:169954737 T 22920 NM_014970.3 Transcript intron_variant - - - - - - rs2474699 1:169954737 T CCDS55661.1 CCDS55661.1 Transcript intron_variant - - - - - - rs2474699 1:169954737 T ENSESTG00000024822 ENSESTT00000063162 Transcript intron_variant - - - - - - rs2474699 1:169954737 T ENSESTG00000024822 ENSESTT00000063071 Transcript intron_variant - - - - - - rs2474699 1:169954737 T ENSESTG00000024822 ENSESTT00000063110 Transcript intron_variant - - - - - - rs2474699 1:169954737 T ENSESTG00000024822 ENSESTT00000063047 Transcript intron_variant - - - - - - rs2474699 1:169954737 T CCDS55659.1 CCDS55659.1 Transcript intron_variant - - - - - - rs2474699 1:169954737 T ENSESTG00000024822 ENSESTT00000063112 Transcript intron_variant - - - - - - rs2474699 1:169954737 T ENSESTG00000024822 ENSESTT00000063155 Transcript intron_variant - - - - - - rs2474699 1:169954737 T 22920 NM_001204517.1 Transcript intron_variant - - - - - - rs2474699 1:169954737 T ENSESTG00000024822 ENSESTT00000063147 Transcript intron_variant - - - - - - rs2474699 1:169954737 T ENSESTG00000024822 ENSESTT00000063116 Transcript intron_variant - - - - - - rs553790 1:170122568 T 149281 NM_001136107.1 Transcript intron_variant - - - - - - rs553790 1:170122568 T CCDS44275.1 CCDS44275.1 Transcript intron_variant - - - - - - rs553790 1:170122568 T 100423010 NR_036065.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1965 rs553790 1:170122568 T 100422839 NR_036064.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1965 rs525326 1:170123357 G 149281 NM_001136107.1 Transcript intron_variant - - - - - - rs525326 1:170123357 G CCDS44275.1 CCDS44275.1 Transcript intron_variant - - - - - - rs525326 1:170123357 G 100423010 NR_036065.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2754 rs525326 1:170123357 G 100422839 NR_036064.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2754 rs471156 1:170125348 A 149281 NM_001136107.1 Transcript intron_variant - - - - - - rs471156 1:170125348 A CCDS44275.1 CCDS44275.1 Transcript intron_variant - - - - - - rs471156 1:170125348 A 100423010 NR_036065.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4745 rs471156 1:170125348 A 100422839 NR_036064.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4745 rs533987 1:170139313 T ENSESTG00000024676 ENSESTT00000062365 Transcript upstream_gene_variant - - - - - - DISTANCE=4220 rs533987 1:170139313 T ENSESTG00000024676 ENSESTT00000062337 Transcript upstream_gene_variant - - - - - - DISTANCE=4207 rs533987 1:170139313 T 149281 NM_001136107.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2390 rs533987 1:170139313 T CCDS44275.1 CCDS44275.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2415 rs533987 1:170139313 T ENSESTG00000024667 ENSESTT00000062320 Transcript downstream_gene_variant - - - - - - DISTANCE=2508 rs6687352 1:170167531 G ENSESTG00000024676 ENSESTT00000062365 Transcript intron_variant - - - - - - rs6687352 1:170167531 G ENSESTG00000024676 ENSESTT00000062337 Transcript intron_variant - - - - - - rs6663366 1:170167601 A ENSESTG00000024676 ENSESTT00000062365 Transcript intron_variant - - - - - - rs6663366 1:170167601 A ENSESTG00000024676 ENSESTT00000062337 Transcript intron_variant - - - - - - rs991627 1:170180274 G ENSESTG00000024676 ENSESTT00000062365 Transcript intron_variant - - - - - - rs991627 1:170180274 G ENSESTG00000024691 ENSESTT00000062393 Transcript intron_variant - - - - - - rs991627 1:170180274 G ENSESTG00000024676 ENSESTT00000062337 Transcript intron_variant - - - - - - rs7548713 1:170276039 G - - - intergenic_variant - - - - - - rs6681969 1:170454457 T ENSESTG00000024705 ENSESTT00000062473 Transcript intron_variant - - - - - - rs6681969 1:170454457 T ENSESTG00000024705 ENSESTT00000062443 Transcript intron_variant - - - - - - rs524779 1:170595038 G - - - intergenic_variant - - - - - - rs6666030 1:170705618 C CCDS1290.1 CCDS1290.1 Transcript downstream_gene_variant - - - - - - DISTANCE=291 rs6666030 1:170705618 C 5396 NM_022716.2 Transcript 3_prime_UTR_variant 1076 - - - - - rs6666030 1:170705618 C 5396 NM_006902.3 Transcript 3_prime_UTR_variant 1148 - - - - - rs6666030 1:170705618 C ENSESTG00000008473 ENSESTT00000021376 Transcript downstream_gene_variant - - - - - - DISTANCE=255 rs6666030 1:170705618 C ENSESTG00000008473 ENSESTT00000021363 Transcript downstream_gene_variant - - - - - - DISTANCE=200 rs6666030 1:170705618 C ENSESTG00000008473 ENSESTT00000021383 Transcript downstream_gene_variant - - - - - - DISTANCE=255 rs4656225 1:170728277 A - - - intergenic_variant - - - - - - rs6666646 1:170733630 T - - - intergenic_variant - - - - - - rs6687857 1:170763285 T - - - intergenic_variant - - - - - - rs6688500 1:170845652 G - - - intergenic_variant - - - - - - rs6663432 1:171441776 C - - - intergenic_variant - - - - - - rs6425288 1:171487266 A 23215 NM_015172.3 Transcript intron_variant - - - - - - rs6425288 1:171487266 A ENSESTG00000008661 ENSESTT00000021797 Transcript intron_variant - - - - - - rs6425288 1:171487266 A ENSESTG00000008661 ENSESTT00000021781 Transcript intron_variant - - - - - - rs6425288 1:171487266 A CCDS1296.2 CCDS1296.2 Transcript intron_variant - - - - - - rs6425288 1:171487266 A ENSESTG00000003189 ENSESTT00000007921 Transcript intron_variant - - - - - - rs2422146 1:172495653 T - - - intergenic_variant - - - - - - rs10798043 1:172502041 G - ENSR00000287142 RegulatoryFeature regulatory_region_variant - - - - - - rs10798043 1:172502041 G 51430 NM_016227.2 Transcript upstream_gene_variant - - - - - - DISTANCE=276 rs10798043 1:172502041 G 51430 NM_014283.3 Transcript upstream_gene_variant - - - - - - DISTANCE=219 rs10798043 1:172502041 G CCDS1303.1 CCDS1303.1 Transcript upstream_gene_variant - - - - - - DISTANCE=535 rs10798043 1:172502041 G ENSESTG00000021547 ENSESTT00000054158 Transcript upstream_gene_variant - - - - - - DISTANCE=217 rs10798043 1:172502041 G ENSESTG00000021547 ENSESTT00000054205 Transcript upstream_gene_variant - - - - - - DISTANCE=282 rs2213711 1:172583617 G 51430 NM_016227.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2644 rs2213711 1:172583617 G 51430 NM_014283.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2644 rs2213711 1:172583617 G CCDS1303.1 CCDS1303.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4218 rs2213711 1:172583617 G ENSESTG00000021607 ENSESTT00000054256 Transcript downstream_gene_variant - - - - - - DISTANCE=3968 rs1041905 1:172616878 G - - - intergenic_variant - - - - - - rs2859243 1:172624910 C ENSESTG00000021628 ENSESTT00000054357 Transcript upstream_gene_variant - - - - - - DISTANCE=3345 rs2859243 1:172624910 C CCDS1304.1 CCDS1304.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3432 rs2859243 1:172624910 C 356 NM_000639.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3275 rs2859244 1:172625207 C ENSESTG00000021628 ENSESTT00000054357 Transcript upstream_gene_variant - - - - - - DISTANCE=3048 rs2859244 1:172625207 C CCDS1304.1 CCDS1304.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3135 rs2859244 1:172625207 C 356 NM_000639.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2978 rs859662 1:172640933 C - ENSR00000547697 RegulatoryFeature regulatory_region_variant - - - - - - rs859662 1:172640933 C 356 NM_000639.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4920 rs859620 1:172688763 C - ENSR00001526065 RegulatoryFeature regulatory_region_variant - - - - - - rs859620 1:172688763 C - - - intergenic_variant - - - - - - rs859646 1:172701510 C - - - intergenic_variant - - - - - - rs6700166 1:172796323 G - - - intergenic_variant - - - - - - rs6684636 1:172796447 G - - - intergenic_variant - - - - - - rs2422258 1:172860848 A - - - intergenic_variant - - - - - - rs7512429 1:172948109 C - - - intergenic_variant - - - - - - rs1160107 1:173079232 A - - - intergenic_variant - - - - - - rs1539264 1:173283107 C 100506023 NR_037845.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1361649 1:173286610 C 100506023 NR_037845.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6686697 1:173316786 G 100506023 NR_037845.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4916217 1:173356650 T 100506023 NR_037845.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2181309 1:173864541 C - - - intergenic_variant - - - - - - rs10912727 1:174059507 A - - - intergenic_variant - - - - - - rs2145377 1:174068058 G - - - intergenic_variant - - - - - - rs12133911 1:174338695 A CCDS1314.1 CCDS1314.1 Transcript intron_variant - - - - - - rs12133911 1:174338695 A 9910 NM_014857.4 Transcript intron_variant - - - - - - rs12133911 1:174338695 A ENSESTG00000010780 ENSESTT00000027011 Transcript intron_variant - - - - - - rs4323661 1:174917683 A ENSESTG00000022531 ENSESTT00000057091 Transcript intron_variant - - - - - - rs4323661 1:174917683 A ENSESTG00000022531 ENSESTT00000057036 Transcript intron_variant - - - - - - rs4323661 1:174917683 A ENSESTG00000022531 ENSESTT00000057011 Transcript intron_variant - - - - - - rs4323661 1:174917683 A CCDS41437.1 CCDS41437.1 Transcript intron_variant - - - - - - rs4323661 1:174917683 A 9910 NM_001243763.1 Transcript intron_variant - - - - - - rs4323661 1:174917683 A ENSESTG00000022531 ENSESTT00000057097 Transcript intron_variant - - - - - - rs4323661 1:174917683 A ENSESTG00000022531 ENSESTT00000057027 Transcript intron_variant - - - - - - rs4323661 1:174917683 A ENSESTG00000022531 ENSESTT00000056972 Transcript intron_variant - - - - - - rs4323661 1:174917683 A ENSESTG00000023271 ENSESTT00000058753 Transcript intron_variant - - - - - - rs4323661 1:174917683 A CCDS58046.1 CCDS58046.1 Transcript intron_variant - - - - - - rs4323661 1:174917683 A CCDS1314.1 CCDS1314.1 Transcript intron_variant - - - - - - rs4323661 1:174917683 A 9910 NM_014857.4 Transcript intron_variant - - - - - - rs4323661 1:174917683 A ENSESTG00000022531 ENSESTT00000057065 Transcript intron_variant - - - - - - rs4323661 1:174917683 A 9910 NM_001035230.2 Transcript intron_variant - - - - - - rs4323661 1:174917683 A 9910 NM_001243765.1 Transcript intron_variant - - - - - - rs6688809 1:174950065 C CCDS55662.1 CCDS55662.1 Transcript intron_variant - - - - - - rs6688809 1:174950065 C ENSESTG00000022531 ENSESTT00000057203 Transcript intron_variant - - - - - - rs6688809 1:174950065 C 9910 NM_001243764.1 Transcript intron_variant - - - - - - rs6688809 1:174950065 C 9910 NM_001243765.1 Transcript intron_variant - - - - - - rs6688809 1:174950065 C CCDS58046.1 CCDS58046.1 Transcript intron_variant - - - - - - rs10449227 1:175259239 T ENSESTG00000023211 ENSESTT00000058578 Transcript intron_variant - - - - - - rs929074 1:175400654 G 7143 NM_003285.2 Transcript intron_variant - - - - - - rs929074 1:175400654 G ENSESTG00000023182 ENSESTT00000058528 Transcript intron_variant - - - - - - rs859414 1:175446788 G 7143 NM_003285.2 Transcript intron_variant - - - - - - rs859414 1:175446788 G ENSESTG00000023182 ENSESTT00000058528 Transcript intron_variant - - - - - - rs1205778 1:175590222 C 7143 NM_003285.2 Transcript intron_variant - - - - - - rs681027 1:176124798 C ENSESTG00000002117 ENSESTT00000005255 Transcript intron_variant - - - - - - rs681027 1:176124798 C ENSESTG00000002117 ENSESTT00000005258 Transcript intron_variant - - - - - - rs681027 1:176124798 C CCDS44279.1 CCDS44279.1 Transcript intron_variant - - - - - - rs681027 1:176124798 C ENSESTG00000002117 ENSESTT00000005253 Transcript intron_variant - - - - - - rs681027 1:176124798 C ENSESTG00000002117 ENSESTT00000005288 Transcript intron_variant - - - - - - rs681027 1:176124798 C ENSESTG00000002117 ENSESTT00000005269 Transcript intron_variant - - - - - - rs681027 1:176124798 C ENSESTG00000002117 ENSESTT00000005279 Transcript intron_variant - - - - - - rs681027 1:176124798 C ENSESTG00000002117 ENSESTT00000005286 Transcript intron_variant - - - - - - rs681027 1:176124798 C ENSESTG00000002117 ENSESTT00000005275 Transcript intron_variant - - - - - - rs681027 1:176124798 C 64326 NM_001001740.2 Transcript intron_variant - - - - - - rs681027 1:176124798 C CCDS30944.1 CCDS30944.1 Transcript intron_variant - - - - - - rs681027 1:176124798 C 64326 NM_022457.5 Transcript intron_variant - - - - - - rs227990 1:176941343 A CCDS44280.1 CCDS44280.1 Transcript intron_variant - - - - - - rs227990 1:176941343 A 460 NM_207108.1 Transcript intron_variant - - - - - - rs227990 1:176941343 A ENSESTG00000024460 ENSESTT00000061896 Transcript intron_variant - - - - - - rs227990 1:176941343 A CCDS1319.1 CCDS1319.1 Transcript intron_variant - - - - - - rs227990 1:176941343 A 460 NM_004319.1 Transcript intron_variant - - - - - - rs227991 1:176941455 A CCDS44280.1 CCDS44280.1 Transcript intron_variant - - - - - - rs227991 1:176941455 A 460 NM_207108.1 Transcript intron_variant - - - - - - rs227991 1:176941455 A ENSESTG00000024460 ENSESTT00000061896 Transcript intron_variant - - - - - - rs227991 1:176941455 A CCDS1319.1 CCDS1319.1 Transcript intron_variant - - - - - - rs227991 1:176941455 A 460 NM_004319.1 Transcript intron_variant - - - - - - rs228018 1:176981491 T CCDS44280.1 CCDS44280.1 Transcript intron_variant - - - - - - rs228018 1:176981491 T 460 NM_207108.1 Transcript intron_variant - - - - - - rs228018 1:176981491 T ENSESTG00000024460 ENSESTT00000061896 Transcript intron_variant - - - - - - rs228018 1:176981491 T CCDS1319.1 CCDS1319.1 Transcript intron_variant - - - - - - rs228018 1:176981491 T 460 NM_004319.1 Transcript intron_variant - - - - - - rs1293346 1:177222610 C ENSESTG00000024351 ENSESTT00000061621 Transcript intron_variant - - - - - - rs1293346 1:177222610 C ENSESTG00000024351 ENSESTT00000061598 Transcript intron_variant - - - - - - rs1293346 1:177222610 C ENSESTG00000024351 ENSESTT00000061635 Transcript upstream_gene_variant - - - - - - DISTANCE=2852 rs1293346 1:177222610 C ENSESTG00000024351 ENSESTT00000061603 Transcript intron_variant - - - - - - rs1293346 1:177222610 C CCDS1320.1 CCDS1320.1 Transcript intron_variant - - - - - - rs1293346 1:177222610 C 57795 NM_021165.2 Transcript intron_variant - - - - - - rs1293346 1:177222610 C ENSESTG00000024351 ENSESTT00000061610 Transcript intron_variant - - - - - - rs1252084 1:177610788 A - - - intergenic_variant - - - - - - rs6678250 1:178041012 G - - - intergenic_variant - - - - - - rs2770155 1:178119799 A - ENSR00001526401 RegulatoryFeature regulatory_region_variant - - - - - - rs2770155 1:178119799 A CCDS1321.2 CCDS1321.2 Transcript intron_variant - - - - - - rs2770155 1:178119799 A ENSESTG00000024159 ENSESTT00000061207 Transcript intron_variant - - - - - - rs2770155 1:178119799 A ENSESTG00000024159 ENSESTT00000061194 Transcript intron_variant - - - - - - rs2770155 1:178119799 A 9462 NM_170692.2 Transcript intron_variant - - - - - - rs445065 1:178420434 T 9462 NM_004841.3 Transcript intron_variant - - - - - - rs445065 1:178420434 T CCDS1321.2 CCDS1321.2 Transcript intron_variant - - - - - - rs445065 1:178420434 T ENSESTG00000024252 ENSESTT00000061349 Transcript upstream_gene_variant - - - - - - DISTANCE=3279 rs445065 1:178420434 T ENSESTG00000024252 ENSESTT00000061323 Transcript upstream_gene_variant - - - - - - DISTANCE=375 rs445065 1:178420434 T CCDS1322.1 CCDS1322.1 Transcript intron_variant - - - - - - rs445065 1:178420434 T 9462 NM_170692.2 Transcript intron_variant - - - - - - rs2473829 1:178466087 G - - - intergenic_variant - - - - - - rs10753182 1:178627655 A ENSESTG00000025718 ENSESTT00000064893 Transcript intron_variant - - - - - - rs2773094 1:178676805 G - - - intergenic_variant - - - - - - rs2773097 1:178689170 C - - - intergenic_variant - - - - - - rs2773081 1:178698151 G ENSESTG00000025816 ENSESTT00000065226 Transcript intron_variant - - - - - - rs2773081 1:178698151 G 55103 NM_152663.3 Transcript intron_variant - - - - - - rs2773081 1:178698151 G ENSESTG00000025816 ENSESTT00000065176 Transcript intron_variant - - - - - - rs2773081 1:178698151 G ENSESTG00000025816 ENSESTT00000065193 Transcript intron_variant - - - - - - rs2773081 1:178698151 G ENSESTG00000025816 ENSESTT00000065230 Transcript intron_variant - - - - - - rs2773081 1:178698151 G ENSESTG00000025816 ENSESTT00000065211 Transcript intron_variant - - - - - - rs6690324 1:178776985 A ENSESTG00000025816 ENSESTT00000065226 Transcript intron_variant - - - - - - rs6690324 1:178776985 A CCDS1325.1 CCDS1325.1 Transcript intron_variant - - - - - - rs6690324 1:178776985 A 55103 NM_152663.3 Transcript intron_variant - - - - - - rs6690324 1:178776985 A ENSESTG00000025816 ENSESTT00000065176 Transcript intron_variant - - - - - - rs6690324 1:178776985 A ENSESTG00000025816 ENSESTT00000065193 Transcript intron_variant - - - - - - rs6690324 1:178776985 A ENSESTG00000025816 ENSESTT00000065230 Transcript intron_variant - - - - - - rs6690324 1:178776985 A ENSESTG00000025816 ENSESTT00000065211 Transcript intron_variant - - - - - - rs6425511 1:178972276 C - ENSR00000081259 RegulatoryFeature regulatory_region_variant - - - - - - rs6425511 1:178972276 C - - - intergenic_variant - - - - - - rs913515 1:179520972 A CCDS30948.1 CCDS30948.1 Transcript intron_variant - - - - - - rs913515 1:179520972 A 126859 NM_144696.4 Transcript intron_variant - - - - - - rs913515 1:179520972 A ENSESTG00000025658 ENSESTT00000064810 Transcript intron_variant - - - - - - rs913515 1:179520972 A 7827 NM_014625.2 Transcript intron_variant - - - - - - rs913515 1:179520972 A ENSESTG00000025658 ENSESTT00000064765 Transcript intron_variant - - - - - - rs913515 1:179520972 A CCDS1331.1 CCDS1331.1 Transcript intron_variant - - - - - - rs913515 1:179520972 A ENSESTG00000025658 ENSESTT00000064822 Transcript upstream_gene_variant - - - - - - DISTANCE=557 rs913515 1:179520972 A ENSESTG00000025658 ENSESTT00000064793 Transcript intron_variant - - - - - - rs656787 1:179932185 C 9857 NM_014810.4 Transcript intron_variant - - - - - - rs656787 1:179932185 C ENSESTG00000026043 ENSESTT00000065689 Transcript intron_variant - - - - - - rs656787 1:179932185 C ENSESTG00000026043 ENSESTT00000065678 Transcript intron_variant - - - - - - rs2040083 1:180022760 T ENSESTG00000026112 ENSESTT00000066189 Transcript intron_variant - - - - - - rs2040083 1:180022760 T 9857 NM_014810.4 Transcript intron_variant - - - - - - rs2040083 1:180022760 T CCDS1336.1 CCDS1336.1 Transcript intron_variant - - - - - - rs2040083 1:180022760 T ENSESTG00000026112 ENSESTT00000066179 Transcript intron_variant - - - - - - rs6683287 1:180419622 G CCDS1339.1 CCDS1339.1 Transcript intron_variant - - - - - - rs6683287 1:180419622 G ENSESTG00000026574 ENSESTT00000067041 Transcript intron_variant - - - - - - rs6683287 1:180419622 G 84320 NM_032360.3 Transcript intron_variant - - - - - - rs7524263 1:180499979 G - ENSR00000548590 RegulatoryFeature regulatory_region_variant - - - - - - rs7524263 1:180499979 G - - - intergenic_variant - - - - - - rs647592 1:181393985 C - ENSR00000287564 RegulatoryFeature regulatory_region_variant - - - - - - rs647592 1:181393985 C ENSESTG00000005188 ENSESTT00000013184 Transcript intron_variant - - - - - - rs2472208 1:181684789 C 777 NM_001205293.1 Transcript intron_variant - - - - - - rs2472208 1:181684789 C ENSESTG00000027725 ENSESTT00000069811 Transcript upstream_gene_variant - - - - - - DISTANCE=4617 rs2472208 1:181684789 C CCDS55665.1 CCDS55665.1 Transcript intron_variant - - - - - - rs2472208 1:181684789 C CCDS55664.1 CCDS55664.1 Transcript intron_variant - - - - - - rs2472208 1:181684789 C ENSESTG00000027711 ENSESTT00000069758 Transcript intron_variant - - - - - - rs2472208 1:181684789 C 777 NM_000721.3 Transcript intron_variant - - - - - - rs2472208 1:181684789 C 777 NM_001205294.1 Transcript intron_variant - - - - - - rs2472208 1:181684789 C CCDS53443.1 CCDS53443.1 Transcript intron_variant - - - - - - rs615251 1:181758375 A 777 NM_001205293.1 Transcript intron_variant - - - - - - rs615251 1:181758375 A 777 NM_000721.3 Transcript intron_variant - - - - - - rs615251 1:181758375 A CCDS55665.1 CCDS55665.1 Transcript intron_variant - - - - - - rs615251 1:181758375 A CCDS53443.1 CCDS53443.1 Transcript intron_variant - - - - - - rs615251 1:181758375 A CCDS55664.1 CCDS55664.1 Transcript intron_variant - - - - - - rs615251 1:181758375 A 777 NM_001205294.1 Transcript intron_variant - - - - - - rs677473 1:181852536 A - - - intergenic_variant - - - - - - rs1281301 1:181918081 G - - - intergenic_variant - - - - - - rs4652694 1:182148307 T - - - intergenic_variant - - - - - - rs1287810 1:182596432 G - - - intergenic_variant - - - - - - rs1148763 1:184163891 G - - - intergenic_variant - - - - - - rs10911601 1:184463777 G CCDS1362.1 CCDS1362.1 Transcript intron_variant - - - - - - rs10911601 1:184463777 G ENSESTG00000019423 ENSESTT00000048867 Transcript intron_variant - - - - - - rs10911601 1:184463777 G ENSESTG00000019423 ENSESTT00000048841 Transcript intron_variant - - - - - - rs10911601 1:184463777 G 81563 NM_030806.3 Transcript intron_variant - - - - - - rs10911601 1:184463777 G ENSESTG00000031166 ENSESTT00000078542 Transcript intron_variant - - - - - - rs9633307 1:184476536 G CCDS1362.1 CCDS1362.1 Transcript intron_variant - - - - - - rs9633307 1:184476536 G ENSESTG00000019423 ENSESTT00000048867 Transcript intron_variant - - - - - - rs9633307 1:184476536 G ENSESTG00000019423 ENSESTT00000048841 Transcript intron_variant - - - - - - rs9633307 1:184476536 G 81563 NM_030806.3 Transcript intron_variant - - - - - - rs9633307 1:184476536 G ENSESTG00000031166 ENSESTT00000078542 Transcript intron_variant - - - - - - rs4651214 1:184479717 G CCDS1362.1 CCDS1362.1 Transcript intron_variant - - - - - - rs4651214 1:184479717 G ENSESTG00000019423 ENSESTT00000048867 Transcript intron_variant - - - - - - rs4651214 1:184479717 G ENSESTG00000019423 ENSESTT00000048841 Transcript intron_variant - - - - - - rs4651214 1:184479717 G 81563 NM_030806.3 Transcript intron_variant - - - - - - rs4651214 1:184479717 G ENSESTG00000031166 ENSESTT00000078542 Transcript intron_variant - - - - - - rs338559 1:184767628 G ENSESTG00000031671 ENSESTT00000080077 Transcript intron_variant - - - - - - rs338559 1:184767628 G 116496 NM_052966.2 Transcript intron_variant - - - - - - rs338559 1:184767628 G ENSESTG00000031671 ENSESTT00000080072 Transcript intron_variant - - - - - - rs338559 1:184767628 G ENSESTG00000031671 ENSESTT00000080053 Transcript intron_variant - - - - - - rs338559 1:184767628 G ENSESTG00000031671 ENSESTT00000080103 Transcript intron_variant - - - - - - rs338559 1:184767628 G CCDS1364.1 CCDS1364.1 Transcript intron_variant - - - - - - rs338559 1:184767628 G ENSESTG00000031671 ENSESTT00000080061 Transcript intron_variant - - - - - - rs338559 1:184767628 G ENSESTG00000031671 ENSESTT00000080116 Transcript intron_variant - - - - - - rs338559 1:184767628 G ENSESTG00000031671 ENSESTT00000080119 Transcript intron_variant - - - - - - rs338559 1:184767628 G ENSESTG00000031671 ENSESTT00000080120 Transcript intron_variant - - - - - - rs338560 1:184771690 C ENSESTG00000031671 ENSESTT00000080077 Transcript intron_variant - - - - - - rs338560 1:184771690 C 116496 NM_052966.2 Transcript intron_variant - - - - - - rs338560 1:184771690 C ENSESTG00000031671 ENSESTT00000080072 Transcript intron_variant - - - - - - rs338560 1:184771690 C ENSESTG00000031671 ENSESTT00000080053 Transcript intron_variant - - - - - - rs338560 1:184771690 C ENSESTG00000031671 ENSESTT00000080103 Transcript intron_variant - - - - - - rs338560 1:184771690 C CCDS1364.1 CCDS1364.1 Transcript intron_variant - - - - - - rs338560 1:184771690 C ENSESTG00000031671 ENSESTT00000080061 Transcript intron_variant - - - - - - rs338560 1:184771690 C ENSESTG00000031671 ENSESTT00000080116 Transcript intron_variant - - - - - - rs338560 1:184771690 C ENSESTG00000031671 ENSESTT00000080119 Transcript intron_variant - - - - - - rs338560 1:184771690 C ENSESTG00000031671 ENSESTT00000080120 Transcript intron_variant - - - - - - rs234118 1:184951784 A - - - intergenic_variant - - - - - - rs10911663 1:184968688 T - - - intergenic_variant - - - - - - rs173017 1:185430464 A - - - intergenic_variant - - - - - - rs685486 1:186136580 G CCDS30956.1 CCDS30956.1 Transcript intron_variant - - - - - - rs685486 1:186136580 G ENSESTG00000010650 ENSESTT00000026665 Transcript intron_variant - - - - - - rs685486 1:186136580 G ENSESTG00000010650 ENSESTT00000026655 Transcript downstream_gene_variant - - - - - - DISTANCE=554 rs685486 1:186136580 G 83872 NM_031935.2 Transcript intron_variant - - - - - - rs685486 1:186136580 G ENSESTG00000010650 ENSESTT00000026669 Transcript intron_variant - - - - - - rs685486 1:186136580 G ENSESTG00000010650 ENSESTT00000026651 Transcript downstream_gene_variant - - - - - - DISTANCE=554 rs68069719 1:186277088 C ENSESTG00000010683 ENSESTT00000026747 Transcript upstream_gene_variant - - - - - - DISTANCE=574 rs68069719 1:186277088 C ENSESTG00000010683 ENSESTT00000026759 Transcript upstream_gene_variant - - - - - - DISTANCE=3478 rs68069719 1:186277088 C ENSESTG00000010683 ENSESTT00000026751 Transcript upstream_gene_variant - - - - - - DISTANCE=574 rs68069719 1:186277088 C CCDS44288.1 CCDS44288.1 Transcript missense_variant 2114 2114 705 C/S tGt/tCt - PolyPhen=unknown rs68069719 1:186277088 C 7175 NM_003292.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3696 rs68069719 1:186277088 C ENSESTG00000010668 ENSESTT00000026707 Transcript intron_variant - - - - - - rs68069719 1:186277088 C 10216 NM_001127710.1 Transcript missense_variant 1886 1835 612 C/S tGt/tCt - rs68069719 1:186277088 C ENSESTG00000010668 ENSESTT00000026710 Transcript downstream_gene_variant - - - - - - DISTANCE=1617 rs68069719 1:186277088 C CCDS44287.1 CCDS44287.1 Transcript missense_variant 1958 1958 653 C/S tGt/tCt - PolyPhen=unknown;SIFT=tolerated rs68069719 1:186277088 C 10216 NM_001127708.1 Transcript missense_variant 2165 2114 705 C/S tGt/tCt - PolyPhen=unknown rs68069719 1:186277088 C CCDS1369.1 CCDS1369.1 Transcript missense_variant 2237 2237 746 C/S tGt/tCt - PolyPhen=unknown rs68069719 1:186277088 C ENSESTG00000010668 ENSESTT00000026712 Transcript intron_variant - - - - - - rs68069719 1:186277088 C 10216 NM_001127709.1 Transcript missense_variant 2009 1958 653 C/S tGt/tCt - PolyPhen=unknown;SIFT=tolerated rs68069719 1:186277088 C 10216 NM_005807.3 Transcript missense_variant 2288 2237 746 C/S tGt/tCt - PolyPhen=unknown rs2853805 1:186641626 A 5743 NM_000963.2 Transcript 3_prime_UTR_variant 3811 - - - - - rs2853805 1:186641626 A ENSESTG00000021240 ENSESTT00000053348 Transcript downstream_gene_variant - - - - - - DISTANCE=2869 rs2853805 1:186641626 A CCDS1371.1 CCDS1371.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1859 rs2179226 1:186708168 G - ENSR00001040571 RegulatoryFeature regulatory_region_variant - - - - - - rs2179226 1:186708168 G - - - intergenic_variant - - - - - - rs6666425 1:186969159 G - - - intergenic_variant - - - - - - rs78520423 1:187068326 T - - - intergenic_variant - - - - - - rs2383657 1:187577714 A ENSESTG00000017412 ENSESTT00000043802 Transcript intron_variant - - - - - - rs1339096 1:187634748 T - - - intergenic_variant - - - - - - rs2495418 1:187772096 A - - - intergenic_variant - - - - - - rs800794 1:187867465 T ENSESTG00000017398 ENSESTT00000043770 Transcript intron_variant - - - - - - rs10159210 1:188406710 T - - - intergenic_variant - - - - - - rs4626886 1:188699158 A - - - intergenic_variant - - - - - - rs2494093 1:189190200 C - ENSR00000671759 RegulatoryFeature regulatory_region_variant - - - - - - rs2494093 1:189190200 C - - - intergenic_variant - - - - - - rs815728 1:189953013 A ENSESTG00000017203 ENSESTT00000043203 Transcript intron_variant - - - - - - rs4845223 1:190008900 T - - - intergenic_variant - - - - - - rs1418812 1:190048492 T - - - intergenic_variant - - - - - - rs703933 1:190464372 G - - - intergenic_variant - - - - - - rs507171 1:190556153 T - - - intergenic_variant - - - - - - rs1931200 1:191284035 T - - - intergenic_variant - - - - - - rs1246706 1:191301640 C - - - intergenic_variant - - - - - - rs1338036 1:191559585 G - - - intergenic_variant - - - - - - rs1246257 1:191599049 G - ENSR00001527042 RegulatoryFeature regulatory_region_variant - - - - - - rs1246257 1:191599049 G - - - intergenic_variant - - - - - - rs4272605 1:192122058 A - - - intergenic_variant - - - - - - rs10458401 1:193077970 C 51022 NM_197962.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3362 rs10458401 1:193077970 C 51022 NM_001243399.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2783 rs10458401 1:193077970 C CCDS1381.1 CCDS1381.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3458 rs10458401 1:193077970 C CCDS1380.1 CCDS1380.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3202 rs10458401 1:193077970 C 51022 NM_016066.4 Transcript upstream_gene_variant - - - - - - DISTANCE=2726 rs10921428 1:193728274 T - - - intergenic_variant - - - - - - rs1328182 1:193758842 C - - - intergenic_variant - - - - - - rs664750 1:194141246 T ENSESTG00000005061 ENSESTT00000012874 Transcript intron_variant - - - - - - rs10737644 1:194390173 A - - - intergenic_variant - - - - - - rs2494346 1:194457821 G - - - intergenic_variant - - - - - - rs79164640 1:194769106 G - - - intergenic_variant - - - - - - rs339643 1:194901076 T - - - intergenic_variant - - - - - - rs1965809 1:195388994 C - - - intergenic_variant - - - - - - rs6428297 1:195667673 A - - - intergenic_variant - - - - - - rs2026969 1:195697279 C - - - intergenic_variant - - - - - - rs10754162 1:195816251 A - - - intergenic_variant - - - - - - rs522637 1:196600862 A - - - intergenic_variant - - - - - - rs203686 1:196676503 T 3075 NM_000186.3 Transcript intron_variant - - - - - - rs203686 1:196676503 T CCDS1385.1 CCDS1385.1 Transcript intron_variant - - - - - - rs203686 1:196676503 T ENSESTG00000018921 ENSESTT00000047991 Transcript intron_variant - - - - - - rs203686 1:196676503 T ENSESTG00000018921 ENSESTT00000047971 Transcript intron_variant - - - - - - rs203686 1:196676503 T ENSESTG00000018921 ENSESTT00000047954 Transcript intron_variant - - - - - - rs203668 1:196691120 A 3075 NM_000186.3 Transcript intron_variant - - - - - - rs203668 1:196691120 A CCDS1385.1 CCDS1385.1 Transcript intron_variant - - - - - - rs203668 1:196691120 A ENSESTG00000018921 ENSESTT00000047971 Transcript intron_variant - - - - - - rs203668 1:196691120 A ENSESTG00000018921 ENSESTT00000047954 Transcript intron_variant - - - - - - rs10801563 1:196769423 G ENSESTG00000019152 ENSESTT00000048169 Transcript intron_variant - - - - - - rs10801563 1:196769423 G ENSESTG00000018921 ENSESTT00000048005 Transcript intron_variant - - - - - - rs10801563 1:196769423 G ENSESTG00000019152 ENSESTT00000048152 Transcript intron_variant - - - - - - rs10801563 1:196769423 G ENSESTG00000018921 ENSESTT00000047954 Transcript intron_variant - - - - - - rs1794009 1:197034005 G ENSESTG00000019572 ENSESTT00000049128 Transcript intron_variant - - - - - - rs1794009 1:197034005 G CCDS1388.1 CCDS1388.1 Transcript intron_variant - - - - - - rs1794009 1:197034005 G 2165 NM_001994.2 Transcript intron_variant - - - - - - rs7520177 1:197096429 T ENSESTG00000019406 ENSESTT00000048795 Transcript upstream_gene_variant - - - - - - DISTANCE=3120 rs7520177 1:197096429 T ENSESTG00000019406 ENSESTT00000048819 Transcript upstream_gene_variant - - - - - - DISTANCE=4850 rs7520177 1:197096429 T CCDS1389.1 CCDS1389.1 Transcript intron_variant - - - - - - rs7520177 1:197096429 T CCDS55672.1 CCDS55672.1 Transcript intron_variant - - - - - - rs7520177 1:197096429 T 259266 NM_018136.4 Transcript intron_variant - - - - - - rs7520177 1:197096429 T 259266 NM_001206846.1 Transcript intron_variant - - - - - - rs7520177 1:197096429 T ENSESTG00000019388 ENSESTT00000048718 Transcript downstream_gene_variant - - - - - - DISTANCE=1890 rs7531835 1:197780622 C - - - intergenic_variant - - - - - - rs1499596 1:197797968 T - - - intergenic_variant - - - - - - rs1499603 1:197879043 C CCDS44290.1 CCDS44290.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2693 rs1499603 1:197879043 C ENSESTG00000018550 ENSESTT00000046709 Transcript downstream_gene_variant - - - - - - DISTANCE=2556 rs1499603 1:197879043 C 56956 NM_001014434.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2592 rs1499603 1:197879043 C 388722 NM_001024594.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2546 rs1499603 1:197879043 C ENSESTG00000018568 ENSESTT00000046731 Transcript upstream_gene_variant - - - - - - DISTANCE=2592 rs1499603 1:197879043 C CCDS30962.1 CCDS30962.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2619 rs1499603 1:197879043 C ENSESTG00000018550 ENSESTT00000046693 Transcript downstream_gene_variant - - - - - - DISTANCE=2556 rs4915253 1:197892793 A 56956 NM_020204.2 Transcript intron_variant - - - - - - rs4915253 1:197892793 A ENSESTG00000018568 ENSESTT00000046741 Transcript downstream_gene_variant - - - - - - DISTANCE=3489 rs4915253 1:197892793 A CCDS1393.1 CCDS1393.1 Transcript intron_variant - - - - - - rs4915253 1:197892793 A ENSESTG00000018587 ENSESTT00000046760 Transcript upstream_gene_variant - - - - - - DISTANCE=4064 rs4915253 1:197892793 A 56956 NM_001014434.1 Transcript intron_variant - - - - - - rs4915253 1:197892793 A ENSESTG00000018568 ENSESTT00000046731 Transcript downstream_gene_variant - - - - - - DISTANCE=2316 rs4915253 1:197892793 A ENSESTG00000018568 ENSESTT00000046750 Transcript downstream_gene_variant - - - - - - DISTANCE=4898 rs4915253 1:197892793 A CCDS30962.1 CCDS30962.1 Transcript intron_variant - - - - - - rs6428424 1:197900023 T ENSESTG00000018587 ENSESTT00000046760 Transcript downstream_gene_variant - - - - - - DISTANCE=1680 rs6428424 1:197900023 T 56956 NM_020204.2 Transcript downstream_gene_variant - - - - - - DISTANCE=750 rs6428424 1:197900023 T 56956 NM_001014434.1 Transcript downstream_gene_variant - - - - - - DISTANCE=750 rs6428424 1:197900023 T CCDS30962.1 CCDS30962.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1634 rs6428424 1:197900023 T CCDS1393.1 CCDS1393.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1634 rs12120898 1:197909898 G - - - intergenic_variant - - - - - - rs6428451 1:198270396 C ENSESTG00000018591 ENSESTT00000046889 Transcript intron_variant - - - - - - rs6428451 1:198270396 C CCDS1394.1 CCDS1394.1 Transcript intron_variant - - - - - - rs6428451 1:198270396 C ENSESTG00000018591 ENSESTT00000046897 Transcript downstream_gene_variant - - - - - - DISTANCE=4024 rs6428451 1:198270396 C ENSESTG00000018591 ENSESTT00000046937 Transcript downstream_gene_variant - - - - - - DISTANCE=4024 rs6428451 1:198270396 C ENSESTG00000018591 ENSESTT00000046936 Transcript intron_variant - - - - - - rs6428451 1:198270396 C 140609 NM_133494.2 Transcript intron_variant - - - - - - rs6428451 1:198270396 C ENSESTG00000018591 ENSESTT00000046917 Transcript intron_variant - - - - - - rs6428451 1:198270396 C ENSESTG00000018591 ENSESTT00000046918 Transcript downstream_gene_variant - - - - - - DISTANCE=4024 rs1409361 1:198589771 G - - - intergenic_variant - - - - - - rs7514665 1:198602361 C - - - intergenic_variant - - - - - - rs4915333 1:198918616 G - - - intergenic_variant - - - - - - rs1275003 1:199078120 T - - - intergenic_variant - - - - - - rs2502137 1:199758609 G - - - intergenic_variant - - - - - - rs2821310 1:200046907 C CCDS1401.1 CCDS1401.1 Transcript intron_variant - - - - - - rs2821310 1:200046907 C CCDS1400.1 CCDS1400.1 Transcript intron_variant - - - - - - rs2821310 1:200046907 C 2494 NM_205860.1 Transcript intron_variant - - - - - - rs2821310 1:200046907 C 2494 NM_003822.3 Transcript intron_variant - - - - - - rs843924 1:200236926 G - - - intergenic_variant - - - - - - rs700463 1:200269738 C - - - intergenic_variant - - - - - - rs4469737 1:200283599 G - ENSR00000550551 RegulatoryFeature regulatory_region_variant - - - - - - rs4469737 1:200283599 G - - - intergenic_variant - - - - - - rs2808235 1:200541873 A CCDS30963.1 CCDS30963.1 Transcript intron_variant - - - - - - rs2808235 1:200541873 A ENSESTG00000003618 ENSESTT00000009045 Transcript intron_variant - - - - - - rs2808235 1:200541873 A 9928 NM_014875.2 Transcript intron_variant - - - - - - rs7411594 1:201034451 A CCDS1407.1 CCDS1407.1 Transcript intron_variant - - - - - - rs7411594 1:201034451 A 779 NM_000069.2 Transcript intron_variant - - - - - - rs1722747 1:201172544 C ENSESTG00000003483 ENSESTT00000008688 Transcript upstream_gene_variant - - - - - - DISTANCE=320 rs1722747 1:201172544 C ENSESTG00000003483 ENSESTT00000008684 Transcript intron_variant - - - - - - rs1722747 1:201172544 C CCDS53455.1 CCDS53455.1 Transcript intron_variant - - - - - - rs1722747 1:201172544 C 91156 NM_001164586.1 Transcript intron_variant - - - - - - rs1256942 1:201395868 C - ENSR00001040706 RegulatoryFeature regulatory_region_variant - - - - - - rs1256942 1:201395868 C 7135 NM_003281.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4994 rs1256942 1:201395868 C ENSESTG00000003532 ENSESTT00000008855 Transcript upstream_gene_variant - - - - - - DISTANCE=4573 rs10920312 1:202016215 G - ENSR00000550898 RegulatoryFeature regulatory_region_variant - - - - - - rs10920312 1:202016215 G - - - intergenic_variant - - - - - - rs788818 1:202263551 G CCDS30971.1 CCDS30971.1 Transcript intron_variant - - - - - - rs788818 1:202263551 G CCDS30972.1 CCDS30972.1 Transcript intron_variant - - - - - - rs788818 1:202263551 G 59352 NM_001017403.1 Transcript intron_variant - - - - - - rs788818 1:202263551 G 59352 NM_001017404.1 Transcript intron_variant - - - - - - rs788818 1:202263551 G CCDS1424.1 CCDS1424.1 Transcript intron_variant - - - - - - rs788818 1:202263551 G 59352 NM_021636.2 Transcript intron_variant - - - - - - rs788818 1:202263551 G ENSESTG00000020312 ENSESTT00000050985 Transcript intron_variant - - - - - - rs705737 1:202444386 C 4660 NM_002481.3 Transcript intron_variant - - - - - - rs705737 1:202444386 C ENSESTG00000023548 ENSESTT00000059369 Transcript intron_variant - - - - - - rs705737 1:202444386 C CCDS1426.1 CCDS1426.1 Transcript intron_variant - - - - - - rs705737 1:202444386 C 4660 NM_032104.2 Transcript intron_variant - - - - - - rs705737 1:202444386 C 4660 NM_032103.2 Transcript intron_variant - - - - - - rs705748 1:202516120 G - ENSR00000550979 RegulatoryFeature regulatory_region_variant - - - - - - rs705748 1:202516120 G 4660 NM_002481.3 Transcript intron_variant - - - - - - rs705748 1:202516120 G 4660 NM_001197131.1 Transcript intron_variant - - - - - - rs705748 1:202516120 G CCDS44295.1 CCDS44295.1 Transcript intron_variant - - - - - - rs705748 1:202516120 G CCDS44294.1 CCDS44294.1 Transcript intron_variant - - - - - - rs705748 1:202516120 G CCDS1426.1 CCDS1426.1 Transcript intron_variant - - - - - - rs705748 1:202516120 G 4660 NM_032104.2 Transcript intron_variant - - - - - - rs705748 1:202516120 G 4660 NM_032103.2 Transcript intron_variant - - - - - - rs585234 1:202573294 G ENSESTG00000024847 ENSESTT00000062784 Transcript downstream_gene_variant - - - - - - DISTANCE=430 rs585234 1:202573294 G ENSESTG00000024847 ENSESTT00000062753 Transcript intron_variant - - - - - - rs585234 1:202573294 G ENSESTG00000024847 ENSESTT00000062770 Transcript downstream_gene_variant - - - - - - DISTANCE=288 rs585234 1:202573294 G 127833 NM_001136504.1 Transcript intron_variant - - - - - - rs585234 1:202573294 G CCDS1427.1 CCDS1427.1 Transcript intron_variant - - - - - - rs585234 1:202573294 G 127833 NM_177402.4 Transcript intron_variant - - - - - - rs566782 1:202605569 A ENSESTG00000024847 ENSESTT00000062784 Transcript intron_variant - - - - - - rs566782 1:202605569 A ENSESTG00000024847 ENSESTT00000062753 Transcript intron_variant - - - - - - rs566782 1:202605569 A ENSESTG00000024847 ENSESTT00000062770 Transcript intron_variant - - - - - - rs566782 1:202605569 A 127833 NM_001136504.1 Transcript intron_variant - - - - - - rs566782 1:202605569 A 127833 NM_177402.4 Transcript intron_variant - - - - - - rs10800879 1:202890293 C ENSESTG00000024358 ENSESTT00000061722 Transcript intron_variant - - - - - - rs10800879 1:202890293 C CCDS1429.1 CCDS1429.1 Transcript intron_variant - - - - - - rs10800879 1:202890293 C ENSESTG00000024358 ENSESTT00000061748 Transcript intron_variant - - - - - - rs10800879 1:202890293 C 59349 NM_021633.2 Transcript intron_variant - - - - - - rs10800879 1:202890293 C ENSESTG00000024358 ENSESTT00000061745 Transcript intron_variant - - - - - - rs10800879 1:202890293 C ENSESTG00000024358 ENSESTT00000061719 Transcript intron_variant - - - - - - rs10800879 1:202890293 C ENSESTG00000024358 ENSESTT00000061678 Transcript intron_variant - - - - - - rs903362 1:203026203 G ENSESTG00000023794 ENSESTT00000060186 Transcript intron_variant - - - - - - rs903362 1:203026203 G ENSESTG00000023794 ENSESTT00000060153 Transcript intron_variant - - - - - - rs903362 1:203026203 G ENSESTG00000023794 ENSESTT00000060163 Transcript intron_variant - - - - - - rs903362 1:203026203 G ENSESTG00000023794 ENSESTT00000060120 Transcript intron_variant - - - - - - rs903362 1:203026203 G CCDS44296.1 CCDS44296.1 Transcript intron_variant - - - - - - rs903362 1:203026203 G ENSESTG00000023794 ENSESTT00000060181 Transcript intron_variant - - - - - - rs903362 1:203026203 G 8497 NM_015053.1 Transcript intron_variant - - - - - - rs903362 1:203026203 G ENSESTG00000023794 ENSESTT00000060148 Transcript intron_variant - - - - - - rs903362 1:203026203 G ENSESTG00000023794 ENSESTT00000060213 Transcript downstream_gene_variant - - - - - - DISTANCE=269 rs9803710 1:203040673 G ENSESTG00000023794 ENSESTT00000060186 Transcript intron_variant - - - - - - rs9803710 1:203040673 G ENSESTG00000023794 ENSESTT00000060153 Transcript intron_variant - - - - - - rs9803710 1:203040673 G ENSESTG00000023794 ENSESTT00000060163 Transcript intron_variant - - - - - - rs9803710 1:203040673 G ENSESTG00000023794 ENSESTT00000060120 Transcript intron_variant - - - - - - rs9803710 1:203040673 G ENSESTG00000023794 ENSESTT00000060232 Transcript intron_variant - - - - - - rs9803710 1:203040673 G CCDS44296.1 CCDS44296.1 Transcript intron_variant - - - - - - rs9803710 1:203040673 G ENSESTG00000023794 ENSESTT00000060181 Transcript intron_variant - - - - - - rs9803710 1:203040673 G ENSESTG00000023794 ENSESTT00000060226 Transcript intron_variant - - - - - - rs9803710 1:203040673 G 8497 NM_015053.1 Transcript intron_variant - - - - - - rs9803710 1:203040673 G ENSESTG00000023794 ENSESTT00000060148 Transcript intron_variant - - - - - - rs9803710 1:203040673 G ENSESTG00000023794 ENSESTT00000060233 Transcript intron_variant - - - - - - rs1494489 1:203122749 C CCDS1434.1 CCDS1434.1 Transcript intron_variant - - - - - - rs1494489 1:203122749 C ENSESTG00000023886 ENSESTT00000060310 Transcript downstream_gene_variant - - - - - - DISTANCE=2862 rs1494489 1:203122749 C ENSESTG00000024167 ENSESTT00000061049 Transcript intron_variant - - - - - - rs1494489 1:203122749 C 134 NM_001048230.1 Transcript intron_variant - - - - - - rs1494489 1:203122749 C ENSESTG00000023886 ENSESTT00000060336 Transcript intron_variant - - - - - - rs1494489 1:203122749 C 134 NM_000674.2 Transcript intron_variant - - - - - - rs1572965 1:203307821 T - ENSR00000162095 RegulatoryFeature regulatory_region_variant - - - - - - rs1572965 1:203307821 T ENSESTG00000023982 ENSESTT00000060643 Transcript downstream_gene_variant - - - - - - DISTANCE=3391 rs1572965 1:203307821 T ENSESTG00000023982 ENSESTT00000060557 Transcript downstream_gene_variant - - - - - - DISTANCE=2825 rs1572965 1:203307821 T ENSESTG00000023982 ENSESTT00000060505 Transcript downstream_gene_variant - - - - - - DISTANCE=3468 rs1572965 1:203307821 T ENSESTG00000023982 ENSESTT00000060518 Transcript downstream_gene_variant - - - - - - DISTANCE=3506 rs1572965 1:203307821 T CCDS30976.1 CCDS30976.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3650 rs1572965 1:203307821 T ENSESTG00000023982 ENSESTT00000060534 Transcript downstream_gene_variant - - - - - - DISTANCE=3286 rs1572965 1:203307821 T ENSESTG00000023982 ENSESTT00000060623 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs1572965 1:203307821 T 2331 NM_002023.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1931 rs6669590 1:203346283 G - - - intergenic_variant - - - - - - rs2027463 1:203368647 G - - - intergenic_variant - - - - - - rs4951350 1:204252513 C ENSESTG00000009750 ENSESTT00000024413 Transcript intron_variant - - - - - - rs4951350 1:204252513 C ENSESTG00000009750 ENSESTT00000024410 Transcript intron_variant - - - - - - rs4951350 1:204252513 C ENSESTG00000009750 ENSESTT00000024417 Transcript intron_variant - - - - - - rs4951350 1:204252513 C ENSESTG00000009750 ENSESTT00000024401 Transcript intron_variant - - - - - - rs4951350 1:204252513 C 22874 NM_014935.4 Transcript intron_variant - - - - - - rs2841631 1:204950709 C 23114 NM_001005388.2 Transcript intron_variant - - - - - - rs2841631 1:204950709 C 23114 NM_001160333.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4435 rs2841631 1:204950709 C CCDS53462.1 CCDS53462.1 Transcript intron_variant - - - - - - rs2841631 1:204950709 C 23114 NM_015090.3 Transcript intron_variant - - - - - - rs2841631 1:204950709 C CCDS53460.1 CCDS53460.1 Transcript intron_variant - - - - - - rs2841631 1:204950709 C 23114 NM_001005389.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4435 rs2841631 1:204950709 C ENSESTG00000011213 ENSESTT00000028089 Transcript upstream_gene_variant - - - - - - DISTANCE=281 rs2841631 1:204950709 C CCDS53461.1 CCDS53461.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4757 rs2841631 1:204950709 C ENSESTG00000011208 ENSESTT00000028077 Transcript downstream_gene_variant - - - - - - DISTANCE=3856 rs2841631 1:204950709 C 23114 NM_001160331.1 Transcript intron_variant - - - - - - rs2841631 1:204950709 C 23114 NM_001160332.1 Transcript intron_variant - - - - - - rs2841631 1:204950709 C CCDS30982.1 CCDS30982.1 Transcript intron_variant - - - - - - rs2841631 1:204950709 C ENSESTG00000011208 ENSESTT00000028079 Transcript downstream_gene_variant - - - - - - DISTANCE=4442 rs7545698 1:205031449 G ENSESTG00000011237 ENSESTT00000028198 Transcript intron_variant - - - - - - rs7545698 1:205031449 G ENSESTG00000011237 ENSESTT00000028188 Transcript intron_variant - - - - - - rs7545698 1:205031449 G ENSESTG00000011223 ENSESTT00000028130 Transcript downstream_gene_variant - - - - - - DISTANCE=2704 rs7545698 1:205031449 G ENSESTG00000011237 ENSESTT00000028203 Transcript intron_variant - - - - - - rs7545698 1:205031449 G ENSESTG00000011237 ENSESTT00000028196 Transcript intron_variant - - - - - - rs7545698 1:205031449 G 6900 NM_005076.3 Transcript intron_variant - - - - - - rs7545698 1:205031449 G ENSESTG00000011223 ENSESTT00000028128 Transcript downstream_gene_variant - - - - - - DISTANCE=3084 rs7545698 1:205031449 G ENSESTG00000011223 ENSESTT00000028129 Transcript downstream_gene_variant - - - - - - DISTANCE=3084 rs7545698 1:205031449 G CCDS1449.1 CCDS1449.1 Transcript intron_variant - - - - - - rs4951193 1:205270407 C - ENSR00000551463 RegulatoryFeature regulatory_region_variant - - - - - - rs4951193 1:205270407 C 81788 NM_030952.1 Transcript downstream_gene_variant - - - - - - DISTANCE=784 rs4951193 1:205270407 C ENSESTG00000011310 ENSESTT00000028420 Transcript downstream_gene_variant - - - - - - DISTANCE=3982 rs4951193 1:205270407 C CCDS1453.1 CCDS1453.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2171 rs1544154 1:205495976 G ENSESTG00000020012 ENSESTT00000050562 Transcript upstream_gene_variant - - - - - - DISTANCE=2417 rs1544154 1:205495976 G CCDS44300.1 CCDS44300.1 Transcript intron_variant - - - - - - rs1544154 1:205495976 G ENSESTG00000020012 ENSESTT00000050549 Transcript downstream_gene_variant - - - - - - DISTANCE=432 rs1544154 1:205495976 G ENSESTG00000020012 ENSESTT00000050526 Transcript missense_variant 963 740 247 Q/R cAg/cGg - rs1544154 1:205495976 G ENSESTG00000020012 ENSESTT00000050493 Transcript intron_variant - - - - - - rs1544154 1:205495976 G CCDS1454.1 CCDS1454.1 Transcript intron_variant - - - - - - rs1544154 1:205495976 G 5129 NM_212502.2 Transcript intron_variant - - - - - - rs1544154 1:205495976 G ENSESTG00000020012 ENSESTT00000050244 Transcript downstream_gene_variant - - - - - - DISTANCE=9 rs1544154 1:205495976 G ENSESTG00000020012 ENSESTT00000050535 Transcript downstream_gene_variant - - - - - - DISTANCE=9 rs1544154 1:205495976 G ENSESTG00000020012 ENSESTT00000050210 Transcript missense_variant 1150 473 158 Q/R cAg/cGg - rs1544154 1:205495976 G 5129 NM_002596.3 Transcript intron_variant - - - - - - rs1544154 1:205495976 G ENSESTG00000020012 ENSESTT00000050520 Transcript intron_variant - - - - - - rs1544154 1:205495976 G 5129 NM_212503.2 Transcript intron_variant - - - - - - rs1544154 1:205495976 G ENSESTG00000020012 ENSESTT00000050508 Transcript intron_variant - - - - - - rs1997803 1:207999043 G - ENSR00000288840 RegulatoryFeature regulatory_region_variant - - - - - - rs1997803 1:207999043 G 148696 NR_026817.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3102 rs1997803 1:207999043 G ENSESTG00000006156 ENSESTT00000015491 Transcript intron_variant - - - - - - rs540265 1:208315040 C ENSESTG00000006111 ENSESTT00000015418 Transcript downstream_gene_variant - - - - - - DISTANCE=672 rs540265 1:208315040 C 5362 NM_025179.3 Transcript intron_variant - - - - - - rs540265 1:208315040 C CCDS31013.1 CCDS31013.1 Transcript intron_variant - - - - - - rs607354 1:208316696 C ENSESTG00000006111 ENSESTT00000015418 Transcript intron_variant - - - - - - rs607354 1:208316696 C 5362 NM_025179.3 Transcript intron_variant - - - - - - rs607354 1:208316696 C CCDS31013.1 CCDS31013.1 Transcript intron_variant - - - - - - rs7368483 1:208917981 C - - - intergenic_variant - - - - - - rs10047076 1:209091680 G - - - intergenic_variant - - - - - - rs6540583 1:210339815 G 255928 NM_001146262.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2179 rs6540583 1:210339815 G 255928 NM_153262.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2179 rs6540583 1:210339815 G 255928 NR_027459.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2179 rs6540583 1:210339815 G 255928 NM_001146261.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2179 rs6540583 1:210339815 G 255928 NM_001146264.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2179 rs6540583 1:210339815 G 255928 NM_001256006.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2179 rs2487910 1:210376109 C - - - intergenic_variant - - - - - - rs654902 1:210434618 C - - - intergenic_variant - - - - - - rs2501906 1:210613722 A - ENSR00001528377 RegulatoryFeature regulatory_region_variant - - - - - - rs2501906 1:210613722 A CCDS1495.1 CCDS1495.1 Transcript intron_variant - - - - - - rs2501906 1:210613722 A CCDS53473.1 CCDS53473.1 Transcript intron_variant - - - - - - rs2501906 1:210613722 A CCDS53471.1 CCDS53471.1 Transcript intron_variant - - - - - - rs2501906 1:210613722 A 55733 NM_001122834.2 Transcript intron_variant - - - - - - rs2501906 1:210613722 A 55733 NM_001170564.1 Transcript intron_variant - - - - - - rs2501906 1:210613722 A 55733 NM_001170588.1 Transcript intron_variant - - - - - - rs2501906 1:210613722 A ENSESTG00000005245 ENSESTT00000013363 Transcript intron_variant - - - - - - rs2501906 1:210613722 A 55733 NM_018194.4 Transcript intron_variant - - - - - - rs2501906 1:210613722 A 55733 NM_001170580.1 Transcript intron_variant - - - - - - rs2501906 1:210613722 A CCDS53472.1 CCDS53472.1 Transcript intron_variant - - - - - - rs2501906 1:210613722 A ENSESTG00000005245 ENSESTT00000013372 Transcript intron_variant - - - - - - rs2501906 1:210613722 A 55733 NM_001170587.1 Transcript intron_variant - - - - - - rs4301631 1:210660584 G CCDS1495.1 CCDS1495.1 Transcript intron_variant - - - - - - rs4301631 1:210660584 G CCDS53473.1 CCDS53473.1 Transcript intron_variant - - - - - - rs4301631 1:210660584 G CCDS53471.1 CCDS53471.1 Transcript intron_variant - - - - - - rs4301631 1:210660584 G 55733 NM_001122834.2 Transcript intron_variant - - - - - - rs4301631 1:210660584 G 55733 NM_001170564.1 Transcript intron_variant - - - - - - rs4301631 1:210660584 G 55733 NM_001170588.1 Transcript intron_variant - - - - - - rs4301631 1:210660584 G ENSESTG00000005245 ENSESTT00000013363 Transcript intron_variant - - - - - - rs4301631 1:210660584 G 55733 NM_018194.4 Transcript intron_variant - - - - - - rs4301631 1:210660584 G 55733 NM_001170580.1 Transcript intron_variant - - - - - - rs4301631 1:210660584 G CCDS53472.1 CCDS53472.1 Transcript intron_variant - - - - - - rs4301631 1:210660584 G ENSESTG00000005245 ENSESTT00000013372 Transcript intron_variant - - - - - - rs4301631 1:210660584 G 55733 NM_001170587.1 Transcript intron_variant - - - - - - rs6540603 1:210703535 C CCDS1495.1 CCDS1495.1 Transcript intron_variant - - - - - - rs6540603 1:210703535 C CCDS53473.1 CCDS53473.1 Transcript intron_variant - - - - - - rs6540603 1:210703535 C CCDS53471.1 CCDS53471.1 Transcript intron_variant - - - - - - rs6540603 1:210703535 C 55733 NM_001122834.2 Transcript intron_variant - - - - - - rs6540603 1:210703535 C 55733 NM_001170564.1 Transcript intron_variant - - - - - - rs6540603 1:210703535 C 55733 NM_001170588.1 Transcript intron_variant - - - - - - rs6540603 1:210703535 C ENSESTG00000005245 ENSESTT00000013363 Transcript intron_variant - - - - - - rs6540603 1:210703535 C 55733 NM_018194.4 Transcript intron_variant - - - - - - rs6540603 1:210703535 C 55733 NM_001170580.1 Transcript intron_variant - - - - - - rs6540603 1:210703535 C CCDS53472.1 CCDS53472.1 Transcript intron_variant - - - - - - rs6540603 1:210703535 C ENSESTG00000005245 ENSESTT00000013372 Transcript intron_variant - - - - - - rs6540603 1:210703535 C 55733 NM_001170587.1 Transcript intron_variant - - - - - - rs4245748 1:210800375 G CCDS1495.1 CCDS1495.1 Transcript intron_variant - - - - - - rs4245748 1:210800375 G CCDS53473.1 CCDS53473.1 Transcript intron_variant - - - - - - rs4245748 1:210800375 G CCDS53471.1 CCDS53471.1 Transcript intron_variant - - - - - - rs4245748 1:210800375 G 55733 NM_001122834.2 Transcript intron_variant - - - - - - rs4245748 1:210800375 G 55733 NM_001170564.1 Transcript intron_variant - - - - - - rs4245748 1:210800375 G 55733 NM_001170588.1 Transcript intron_variant - - - - - - rs4245748 1:210800375 G ENSESTG00000005245 ENSESTT00000013363 Transcript downstream_gene_variant - - - - - - DISTANCE=3417 rs4245748 1:210800375 G 55733 NM_018194.4 Transcript intron_variant - - - - - - rs4245748 1:210800375 G 55733 NM_001170580.1 Transcript intron_variant - - - - - - rs4245748 1:210800375 G CCDS53472.1 CCDS53472.1 Transcript intron_variant - - - - - - rs4245748 1:210800375 G 55733 NM_001170587.1 Transcript intron_variant - - - - - - rs4245748 1:210800375 G ENSESTG00000005245 ENSESTT00000013389 Transcript intron_variant - - - - - - rs4534454 1:211042914 T CCDS31015.1 CCDS31015.1 Transcript intron_variant - - - - - - rs4534454 1:211042914 T 3756 NM_002238.3 Transcript intron_variant - - - - - - rs4534454 1:211042914 T 3756 NM_172362.2 Transcript intron_variant - - - - - - rs4534454 1:211042914 T CCDS1496.1 CCDS1496.1 Transcript intron_variant - - - - - - rs4304648 1:211725741 C - ENSR00001040876 RegulatoryFeature regulatory_region_variant - - - - - - rs4304648 1:211725741 C - - - intergenic_variant - - - - - - rs6540696 1:211804952 C - - - intergenic_variant - - - - - - rs4951667 1:213260904 G ENSESTG00000026608 ENSESTT00000067208 Transcript intron_variant - - - - - - rs4951667 1:213260904 G CCDS44317.1 CCDS44317.1 Transcript intron_variant - - - - - - rs4951667 1:213260904 G ENSESTG00000026608 ENSESTT00000067107 Transcript intron_variant - - - - - - rs4951667 1:213260904 G ENSESTG00000026608 ENSESTT00000067174 Transcript intron_variant - - - - - - rs4951667 1:213260904 G 26750 NM_012424.3 Transcript intron_variant - - - - - - rs4951667 1:213260904 G ENSESTG00000026608 ENSESTT00000067206 Transcript intron_variant - - - - - - rs4951667 1:213260904 G ENSESTG00000026608 ENSESTT00000067204 Transcript intron_variant - - - - - - rs4951667 1:213260904 G ENSESTG00000026608 ENSESTT00000067216 Transcript intron_variant - - - - - - rs4951667 1:213260904 G ENSESTG00000026608 ENSESTT00000067167 Transcript intron_variant - - - - - - rs4951667 1:213260904 G CCDS1513.1 CCDS1513.1 Transcript intron_variant - - - - - - rs4951667 1:213260904 G 26750 NM_001136138.1 Transcript intron_variant - - - - - - rs2793277 1:213921330 A ENSESTG00000024372 ENSESTT00000061630 Transcript intron_variant - - - - - - rs1972330 1:214228679 A - - - intergenic_variant - - - - - - rs6540828 1:214553672 T CCDS1514.1 CCDS1514.1 Transcript intron_variant - - - - - - rs6540828 1:214553672 T ENSESTG00000005163 ENSESTT00000013115 Transcript intron_variant - - - - - - rs6540828 1:214553672 T 5784 NM_005401.4 Transcript intron_variant - - - - - - rs6540828 1:214553672 T ENSESTG00000005156 ENSESTT00000013105 Transcript downstream_gene_variant - - - - - - DISTANCE=4034 rs1779685 1:214966001 T - - - intergenic_variant - - - - - - rs4098469 1:215456729 A - - - intergenic_variant - - - - - - rs10864172 1:215463929 T - - - intergenic_variant - - - - - - rs6679790 1:215635400 T - - - intergenic_variant - - - - - - rs1066190 1:216455897 C 7399 NM_007123.5 Transcript intron_variant - - - - - - rs1066190 1:216455897 C CCDS31025.1 CCDS31025.1 Transcript intron_variant - - - - - - rs1066190 1:216455897 C CCDS1516.1 CCDS1516.1 Transcript intron_variant - - - - - - rs1066190 1:216455897 C 7399 NM_206933.2 Transcript intron_variant - - - - - - rs4240938 1:217432620 T - - - intergenic_variant - - - - - - rs10779296 1:217626035 A 55105 NM_018040.2 Transcript intron_variant - - - - - - rs10779296 1:217626035 A ENSESTG00000032704 ENSESTT00000082612 Transcript intron_variant - - - - - - rs10779296 1:217626035 A CCDS1518.1 CCDS1518.1 Transcript intron_variant - - - - - - rs265124 1:217626399 A 55105 NM_018040.2 Transcript intron_variant - - - - - - rs265124 1:217626399 A ENSESTG00000032704 ENSESTT00000082612 Transcript intron_variant - - - - - - rs265124 1:217626399 A CCDS1518.1 CCDS1518.1 Transcript intron_variant - - - - - - rs1930298 1:217779170 A - ENSR00000553080 RegulatoryFeature regulatory_region_variant - - - - - - rs1930298 1:217779170 A 55105 NM_018040.2 Transcript intron_variant - - - - - - rs1930298 1:217779170 A ENSESTG00000032698 ENSESTT00000082594 Transcript intron_variant - - - - - - rs1930298 1:217779170 A CCDS1518.1 CCDS1518.1 Transcript intron_variant - - - - - - rs6682167 1:217964245 G ENSESTG00000032625 ENSESTT00000082497 Transcript intron_variant - - - - - - rs6682167 1:217964245 G CCDS1519.1 CCDS1519.1 Transcript intron_variant - - - - - - rs6682167 1:217964245 G 128153 NM_138796.2 Transcript intron_variant - - - - - - rs6682167 1:217964245 G ENSESTG00000032625 ENSESTT00000082522 Transcript intron_variant - - - - - - rs1023290 1:218223322 G - - - intergenic_variant - - - - - - rs1953755 1:218384775 T - - - intergenic_variant - - - - - - rs1690787 1:218689790 A - - - intergenic_variant - - - - - - rs1625729 1:219217852 T ENSESTG00000003412 ENSESTT00000008529 Transcript downstream_gene_variant - - - - - - DISTANCE=4632 rs1256636 1:219237703 G ENSESTG00000003412 ENSESTT00000008529 Transcript intron_variant - - - - - - rs10779378 1:219896201 G ENSESTG00000029774 ENSESTT00000074903 Transcript intron_variant - - - - - - rs1774012 1:220098618 G 55532 NM_018713.2 Transcript intron_variant - - - - - - rs1774012 1:220098618 G 55532 NR_046437.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1774012 1:220098618 G CCDS31026.1 CCDS31026.1 Transcript intron_variant - - - - - - rs1774012 1:220098618 G ENSESTG00000029765 ENSESTT00000074875 Transcript intron_variant - - - - - - rs1612813 1:220243002 G ENSESTG00000029321 ENSESTT00000074014 Transcript intron_variant - - - - - - rs1612813 1:220243002 G ENSESTG00000029321 ENSESTT00000073999 Transcript intron_variant - - - - - - rs1612813 1:220243002 G ENSESTG00000029321 ENSESTT00000073941 Transcript intron_variant - - - - - - rs1612813 1:220243002 G CCDS41469.1 CCDS41469.1 Transcript intron_variant - - - - - - rs1612813 1:220243002 G ENSESTG00000029321 ENSESTT00000073902 Transcript intron_variant - - - - - - rs1612813 1:220243002 G ENSESTG00000029321 ENSESTT00000073934 Transcript intron_variant - - - - - - rs1612813 1:220243002 G ENSESTG00000029321 ENSESTT00000073973 Transcript intron_variant - - - - - - rs1612813 1:220243002 G 10380 NM_006085.4 Transcript intron_variant - - - - - - rs1612813 1:220243002 G ENSESTG00000029321 ENSESTT00000073917 Transcript intron_variant - - - - - - rs1612813 1:220243002 G ENSESTG00000029321 ENSESTT00000074038 Transcript intron_variant - - - - - - rs4307574 1:220393756 C - ENSR00001529048 RegulatoryFeature regulatory_region_variant - - - - - - rs4307574 1:220393756 C ENSESTG00000014093 ENSESTT00000035272 Transcript intron_variant - - - - - - rs4307574 1:220393756 C 25782 NM_012414.3 Transcript intron_variant - - - - - - rs4307574 1:220393756 C ENSESTG00000014093 ENSESTT00000035300 Transcript intron_variant - - - - - - rs4307574 1:220393756 C CCDS31028.1 CCDS31028.1 Transcript intron_variant - - - - - - rs4307574 1:220393756 C ENSESTG00000014093 ENSESTT00000035246 Transcript intron_variant - - - - - - rs4307574 1:220393756 C ENSESTG00000014093 ENSESTT00000035276 Transcript intron_variant - - - - - - rs4307574 1:220393756 C ENSESTG00000014093 ENSESTT00000035292 Transcript intron_variant - - - - - - rs4427410 1:221139365 G - - - intergenic_variant - - - - - - rs2784261 1:221151581 A - - - intergenic_variant - - - - - - rs61840293 1:223068588 G 84976 NM_032890.3 Transcript intron_variant - - - - - - rs61840293 1:223068588 G ENSESTG00000017547 ENSESTT00000044202 Transcript intron_variant - - - - - - rs1339462 1:223167764 A - ENSR00000553737 RegulatoryFeature regulatory_region_variant - - - - - - rs1339462 1:223167764 A CCDS1536.1 CCDS1536.1 Transcript intron_variant - - - - - - rs1339462 1:223167764 A 84976 NM_032890.3 Transcript intron_variant - - - - - - rs1339462 1:223167764 A ENSESTG00000017547 ENSESTT00000044202 Transcript intron_variant - - - - - - rs1339462 1:223167764 A ENSESTG00000017547 ENSESTT00000044216 Transcript intron_variant - - - - - - rs1339462 1:223167764 A ENSESTG00000017547 ENSESTT00000044211 Transcript intron_variant - - - - - - rs1339462 1:223167764 A ENSESTG00000017547 ENSESTT00000044235 Transcript intron_variant - - - - - - rs2926155 1:223181275 C CCDS1536.1 CCDS1536.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1961 rs2926155 1:223181275 C 84976 NM_032890.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1938 rs2926155 1:223181275 C ENSESTG00000017547 ENSESTT00000044202 Transcript downstream_gene_variant - - - - - - DISTANCE=4449 rs2926155 1:223181275 C ENSESTG00000017547 ENSESTT00000044216 Transcript downstream_gene_variant - - - - - - DISTANCE=4449 rs2926155 1:223181275 C ENSESTG00000017547 ENSESTT00000044211 Transcript downstream_gene_variant - - - - - - DISTANCE=4449 rs2926155 1:223181275 C ENSESTG00000017547 ENSESTT00000044235 Transcript downstream_gene_variant - - - - - - DISTANCE=2694 rs7512943 1:223283910 G ENSESTG00000017591 ENSESTT00000044276 Transcript downstream_gene_variant - - - - - - DISTANCE=2400 rs7512943 1:223283910 G CCDS31033.1 CCDS31033.1 Transcript missense_variant 2464 2464 822 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs7512943 1:223283910 G 7100 NM_003268.5 Transcript missense_variant 3105 2464 822 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs825120 1:223472573 G ENSESTG00000009551 ENSESTT00000024028 Transcript intron_variant - - - - - - rs825120 1:223472573 G ENSESTG00000009551 ENSESTT00000023983 Transcript intron_variant - - - - - - rs825120 1:223472573 G 55061 NM_017982.3 Transcript intron_variant - - - - - - rs825120 1:223472573 G ENSESTG00000009551 ENSESTT00000023979 Transcript intron_variant - - - - - - rs825120 1:223472573 G CCDS41471.1 CCDS41471.1 Transcript intron_variant - - - - - - rs825120 1:223472573 G 55061 NM_001037175.2 Transcript intron_variant - - - - - - rs825120 1:223472573 G CCDS31034.1 CCDS31034.1 Transcript intron_variant - - - - - - rs825120 1:223472573 G ENSESTG00000009551 ENSESTT00000023990 Transcript intron_variant - - - - - - rs825120 1:223472573 G ENSESTG00000009551 ENSESTT00000023995 Transcript intron_variant - - - - - - rs1103973 1:223581334 C - - - intergenic_variant - - - - - - rs10752442 1:223640664 G - - - intergenic_variant - - - - - - rs4612620 1:223662766 C - - - intergenic_variant - - - - - - rs7417403 1:223664300 C - - - intergenic_variant - - - - - - rs6670935 1:223682815 G - - - intergenic_variant - - - - - - rs4421578 1:223688208 G - ENSR00001529327 RegulatoryFeature regulatory_region_variant - - - - - - rs4421578 1:223688208 G - - - intergenic_variant - - - - - - rs2404353 1:223826005 A 388743 NM_001143962.1 Transcript intron_variant - - - - - - rs2404353 1:223826005 A ENSESTG00000009538 ENSESTT00000023925 Transcript intron_variant - - - - - - rs2404353 1:223826005 A ENSESTG00000009538 ENSESTT00000023918 Transcript intron_variant - - - - - - rs1892078 1:223837244 A 388743 NM_001143962.1 Transcript intron_variant - - - - - - rs1892078 1:223837244 A ENSESTG00000009538 ENSESTT00000023925 Transcript intron_variant - - - - - - rs1892078 1:223837244 A ENSESTG00000009538 ENSESTT00000023918 Transcript intron_variant - - - - - - rs4653858 1:223868359 G - - - intergenic_variant - - - - - - rs6604734 1:223870556 G - - - intergenic_variant - - - - - - rs6675957 1:223873928 A - - - intergenic_variant - - - - - - rs1222132 1:223935090 C CCDS53478.1 CCDS53478.1 Transcript intron_variant - - - - - - rs1222132 1:223935090 C ENSESTG00000009309 ENSESTT00000023522 Transcript upstream_gene_variant - - - - - - DISTANCE=1173 rs1222132 1:223935090 C ENSESTG00000009309 ENSESTT00000023404 Transcript intron_variant - - - - - - rs1222132 1:223935090 C ENSESTG00000009309 ENSESTT00000023516 Transcript intron_variant - - - - - - rs1222132 1:223935090 C 824 NM_001748.4 Transcript intron_variant - - - - - - rs1222132 1:223935090 C ENSESTG00000009309 ENSESTT00000023507 Transcript intron_variant - - - - - - rs1222132 1:223935090 C CCDS31035.1 CCDS31035.1 Transcript intron_variant - - - - - - rs1222132 1:223935090 C ENSESTG00000009309 ENSESTT00000023514 Transcript intron_variant - - - - - - rs1222132 1:223935090 C 824 NM_001146068.1 Transcript intron_variant - - - - - - rs1222132 1:223935090 C ENSESTG00000009309 ENSESTT00000023495 Transcript intron_variant - - - - - - rs4653505 1:224243663 G - - - intergenic_variant - - - - - - rs6694306 1:224299242 G ENSESTG00000009437 ENSESTT00000023675 Transcript upstream_gene_variant - - - - - - DISTANCE=2553 rs6694306 1:224299242 G 23219 NM_015176.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2547 rs6694306 1:224299242 G CCDS44320.1 CCDS44320.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2590 rs6694306 1:224299242 G CCDS1539.1 CCDS1539.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2590 rs6694306 1:224299242 G ENSESTG00000009437 ENSESTT00000023678 Transcript upstream_gene_variant - - - - - - DISTANCE=2678 rs6694306 1:224299242 G 23219 NR_049764.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2547 rs6694306 1:224299242 G ENSESTG00000009437 ENSESTT00000023674 Transcript upstream_gene_variant - - - - - - DISTANCE=2553 rs6694306 1:224299242 G 23219 NM_001136115.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2547 rs1533590 1:224421989 A CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs1533590 1:224421989 A ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs1533590 1:224421989 A 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs1533590 1:224421989 A CCDS1542.1 CCDS1542.1 Transcript intron_variant - - - - - - rs1533590 1:224421989 A CCDS58062.1 CCDS58062.1 Transcript intron_variant - - - - - - rs1533590 1:224421989 A 4931 NM_206840.2 Transcript intron_variant - - - - - - rs1533590 1:224421989 A ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs1533590 1:224421989 A 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs1533590 1:224421989 A 4931 NM_002533.3 Transcript intron_variant - - - - - - rs1533590 1:224421989 A CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs1533590 1:224421989 A ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs1533590 1:224421989 A ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs1533590 1:224421989 A ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs1533590 1:224421989 A ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs7518299 1:224443424 C CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs7518299 1:224443424 C ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs7518299 1:224443424 C 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs7518299 1:224443424 C CCDS1542.1 CCDS1542.1 Transcript intron_variant - - - - - - rs7518299 1:224443424 C CCDS58062.1 CCDS58062.1 Transcript intron_variant - - - - - - rs7518299 1:224443424 C 4931 NM_206840.2 Transcript intron_variant - - - - - - rs7518299 1:224443424 C 100313769 NR_031574.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1282 rs7518299 1:224443424 C ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs7518299 1:224443424 C 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs7518299 1:224443424 C 4931 NM_002533.3 Transcript intron_variant - - - - - - rs7518299 1:224443424 C CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs7518299 1:224443424 C ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs7518299 1:224443424 C ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs7518299 1:224443424 C ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs7518299 1:224443424 C ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs2897055 1:224444901 C CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs2897055 1:224444901 C ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs2897055 1:224444901 C 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs2897055 1:224444901 C CCDS1542.1 CCDS1542.1 Transcript intron_variant - - - - - - rs2897055 1:224444901 C CCDS58062.1 CCDS58062.1 Transcript intron_variant - - - - - - rs2897055 1:224444901 C 4931 NM_206840.2 Transcript intron_variant - - - - - - rs2897055 1:224444901 C 100313769 NR_031574.1 Transcript upstream_gene_variant - - - - - - DISTANCE=58 rs2897055 1:224444901 C ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs2897055 1:224444901 C 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs2897055 1:224444901 C 4931 NM_002533.3 Transcript intron_variant - - - - - - rs2897055 1:224444901 C CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs2897055 1:224444901 C ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs2897055 1:224444901 C ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs2897055 1:224444901 C ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs2897055 1:224444901 C ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs2405063 1:224444982 C CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs2405063 1:224444982 C ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs2405063 1:224444982 C 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs2405063 1:224444982 C CCDS1542.1 CCDS1542.1 Transcript intron_variant - - - - - - rs2405063 1:224444982 C CCDS58062.1 CCDS58062.1 Transcript intron_variant - - - - - - rs2405063 1:224444982 C 4931 NM_206840.2 Transcript intron_variant - - - - - - rs2405063 1:224444982 C 100313769 NR_031574.1 Transcript upstream_gene_variant - - - - - - DISTANCE=139 rs2405063 1:224444982 C ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs2405063 1:224444982 C 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs2405063 1:224444982 C 4931 NM_002533.3 Transcript intron_variant - - - - - - rs2405063 1:224444982 C CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs2405063 1:224444982 C ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs2405063 1:224444982 C ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs2405063 1:224444982 C ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs2405063 1:224444982 C ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs10799557 1:224451865 C CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs10799557 1:224451865 C ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs10799557 1:224451865 C 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs10799557 1:224451865 C CCDS1542.1 CCDS1542.1 Transcript intron_variant - - - - - - rs10799557 1:224451865 C CCDS58062.1 CCDS58062.1 Transcript intron_variant - - - - - - rs10799557 1:224451865 C 4931 NM_206840.2 Transcript intron_variant - - - - - - rs10799557 1:224451865 C ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs10799557 1:224451865 C 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs10799557 1:224451865 C 4931 NM_002533.3 Transcript intron_variant - - - - - - rs10799557 1:224451865 C CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs10799557 1:224451865 C ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs10799557 1:224451865 C ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs10799557 1:224451865 C ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs10799557 1:224451865 C ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs12121597 1:224464784 C CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs12121597 1:224464784 C ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs12121597 1:224464784 C 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs12121597 1:224464784 C CCDS1542.1 CCDS1542.1 Transcript intron_variant - - - - - - rs12121597 1:224464784 C CCDS58062.1 CCDS58062.1 Transcript intron_variant - - - - - - rs12121597 1:224464784 C 4931 NM_206840.2 Transcript intron_variant - - - - - - rs12121597 1:224464784 C ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs12121597 1:224464784 C 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs12121597 1:224464784 C 4931 NM_002533.3 Transcript intron_variant - - - - - - rs12121597 1:224464784 C CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs12121597 1:224464784 C ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs12121597 1:224464784 C ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs12121597 1:224464784 C ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs12121597 1:224464784 C ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs10799558 1:224470443 C CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs10799558 1:224470443 C ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs10799558 1:224470443 C 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs10799558 1:224470443 C CCDS1542.1 CCDS1542.1 Transcript intron_variant - - - - - - rs10799558 1:224470443 C CCDS58062.1 CCDS58062.1 Transcript intron_variant - - - - - - rs10799558 1:224470443 C 4931 NM_206840.2 Transcript intron_variant - - - - - - rs10799558 1:224470443 C ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs10799558 1:224470443 C 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs10799558 1:224470443 C 4931 NM_002533.3 Transcript intron_variant - - - - - - rs10799558 1:224470443 C CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs10799558 1:224470443 C ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs10799558 1:224470443 C ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs10799558 1:224470443 C ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs10799558 1:224470443 C ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs10916582 1:224485588 A CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs10916582 1:224485588 A ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs10916582 1:224485588 A 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs10916582 1:224485588 A CCDS1542.1 CCDS1542.1 Transcript intron_variant - - - - - - rs10916582 1:224485588 A CCDS58062.1 CCDS58062.1 Transcript intron_variant - - - - - - rs10916582 1:224485588 A 4931 NM_206840.2 Transcript intron_variant - - - - - - rs10916582 1:224485588 A ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs10916582 1:224485588 A 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs10916582 1:224485588 A 4931 NM_002533.3 Transcript intron_variant - - - - - - rs10916582 1:224485588 A CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs10916582 1:224485588 A ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs10916582 1:224485588 A ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs10916582 1:224485588 A ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs10916582 1:224485588 A ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs7532244 1:224493002 C CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs7532244 1:224493002 C ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs7532244 1:224493002 C 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs7532244 1:224493002 C CCDS1542.1 CCDS1542.1 Transcript intron_variant - - - - - - rs7532244 1:224493002 C CCDS58062.1 CCDS58062.1 Transcript upstream_gene_variant - - - - - - DISTANCE=167 rs7532244 1:224493002 C 4931 NM_206840.2 Transcript intron_variant - - - - - - rs7532244 1:224493002 C ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs7532244 1:224493002 C 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs7532244 1:224493002 C 4931 NM_002533.3 Transcript intron_variant - - - - - - rs7532244 1:224493002 C CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs7532244 1:224493002 C ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs7532244 1:224493002 C ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs7532244 1:224493002 C ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs7532244 1:224493002 C ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs7537492 1:224505043 A CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs7537492 1:224505043 A ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs7537492 1:224505043 A ENSESTG00000020170 ENSESTT00000051031 Transcript intron_variant - - - - - - rs7537492 1:224505043 A 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs7537492 1:224505043 A ENSESTG00000020170 ENSESTT00000051012 Transcript intron_variant - - - - - - rs7537492 1:224505043 A 4931 NM_206840.2 Transcript intron_variant - - - - - - rs7537492 1:224505043 A ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs7537492 1:224505043 A 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs7537492 1:224505043 A 4931 NM_002533.3 Transcript intron_variant - - - - - - rs7537492 1:224505043 A CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs7537492 1:224505043 A ENSESTG00000020170 ENSESTT00000050998 Transcript intron_variant - - - - - - rs7537492 1:224505043 A ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs7537492 1:224505043 A ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs7537492 1:224505043 A ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs7537492 1:224505043 A ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs4654021 1:224511892 A CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs4654021 1:224511892 A ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs4654021 1:224511892 A ENSESTG00000020170 ENSESTT00000051031 Transcript intron_variant - - - - - - rs4654021 1:224511892 A 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs4654021 1:224511892 A ENSESTG00000020170 ENSESTT00000051012 Transcript intron_variant - - - - - - rs4654021 1:224511892 A 4931 NM_206840.2 Transcript intron_variant - - - - - - rs4654021 1:224511892 A ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs4654021 1:224511892 A 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs4654021 1:224511892 A 4931 NM_002533.3 Transcript intron_variant - - - - - - rs4654021 1:224511892 A CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs4654021 1:224511892 A ENSESTG00000020170 ENSESTT00000050998 Transcript intron_variant - - - - - - rs4654021 1:224511892 A ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs4654021 1:224511892 A ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs4654021 1:224511892 A ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs4654021 1:224511892 A ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs4653578 1:224514275 A CCDS1541.1 CCDS1541.1 Transcript intron_variant - - - - - - rs4653578 1:224514275 A ENSESTG00000020170 ENSESTT00000051068 Transcript intron_variant - - - - - - rs4653578 1:224514275 A ENSESTG00000020170 ENSESTT00000051031 Transcript intron_variant - - - - - - rs4653578 1:224514275 A 4931 NM_001243147.1 Transcript intron_variant - - - - - - rs4653578 1:224514275 A ENSESTG00000020170 ENSESTT00000051012 Transcript intron_variant - - - - - - rs4653578 1:224514275 A 4931 NM_206840.2 Transcript intron_variant - - - - - - rs4653578 1:224514275 A ENSESTG00000020170 ENSESTT00000051041 Transcript intron_variant - - - - - - rs4653578 1:224514275 A 4931 NM_001243146.1 Transcript intron_variant - - - - - - rs4653578 1:224514275 A 4931 NM_002533.3 Transcript intron_variant - - - - - - rs4653578 1:224514275 A CCDS58063.1 CCDS58063.1 Transcript intron_variant - - - - - - rs4653578 1:224514275 A ENSESTG00000020170 ENSESTT00000050998 Transcript intron_variant - - - - - - rs4653578 1:224514275 A ENSESTG00000020170 ENSESTT00000050846 Transcript intron_variant - - - - - - rs4653578 1:224514275 A ENSESTG00000020170 ENSESTT00000050891 Transcript intron_variant - - - - - - rs4653578 1:224514275 A ENSESTG00000020170 ENSESTT00000050977 Transcript intron_variant - - - - - - rs4653578 1:224514275 A ENSESTG00000020170 ENSESTT00000050981 Transcript intron_variant - - - - - - rs2404855 1:224521112 G - ENSR00000289498 RegulatoryFeature regulatory_region_variant - - - - - - rs2404855 1:224521112 G CCDS1541.1 CCDS1541.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3283 rs2404855 1:224521112 G ENSESTG00000020170 ENSESTT00000051068 Transcript upstream_gene_variant - - - - - - DISTANCE=3272 rs2404855 1:224521112 G ENSESTG00000020170 ENSESTT00000051031 Transcript upstream_gene_variant - - - - - - DISTANCE=3257 rs2404855 1:224521112 G 4931 NM_001243147.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3221 rs2404855 1:224521112 G ENSESTG00000020170 ENSESTT00000051012 Transcript upstream_gene_variant - - - - - - DISTANCE=3238 rs2404855 1:224521112 G 4931 NM_206840.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3221 rs2404855 1:224521112 G ENSESTG00000020170 ENSESTT00000051041 Transcript upstream_gene_variant - - - - - - DISTANCE=3272 rs2404855 1:224521112 G 4931 NM_001243146.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3221 rs2404855 1:224521112 G 4931 NM_002533.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3221 rs2404855 1:224521112 G CCDS58063.1 CCDS58063.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3283 rs2404855 1:224521112 G ENSESTG00000020170 ENSESTT00000050998 Transcript upstream_gene_variant - - - - - - DISTANCE=3234 rs2404855 1:224521112 G ENSESTG00000020170 ENSESTT00000050846 Transcript upstream_gene_variant - - - - - - DISTANCE=3209 rs2404855 1:224521112 G ENSESTG00000020170 ENSESTT00000050891 Transcript upstream_gene_variant - - - - - - DISTANCE=3209 rs2404855 1:224521112 G ENSESTG00000020170 ENSESTT00000050977 Transcript upstream_gene_variant - - - - - - DISTANCE=3234 rs2404855 1:224521112 G ENSESTG00000020170 ENSESTT00000050981 Transcript upstream_gene_variant - - - - - - DISTANCE=3234 rs2501119 1:225207311 A ENSESTG00000020029 ENSESTT00000050197 Transcript intron_variant - - - - - - rs2501119 1:225207311 A CCDS44322.1 CCDS44322.1 Transcript intron_variant - - - - - - rs2501119 1:225207311 A 127602 NM_001145154.1 Transcript intron_variant - - - - - - rs2501119 1:225207311 A 127602 NM_001373.1 Transcript intron_variant - - - - - - rs2501116 1:225209023 A ENSESTG00000020029 ENSESTT00000050197 Transcript intron_variant - - - - - - rs2501116 1:225209023 A CCDS44322.1 CCDS44322.1 Transcript intron_variant - - - - - - rs2501116 1:225209023 A 127602 NM_001145154.1 Transcript intron_variant - - - - - - rs2501116 1:225209023 A 127602 NM_001373.1 Transcript intron_variant - - - - - - rs2501105 1:225231117 G ENSESTG00000020029 ENSESTT00000050197 Transcript downstream_gene_variant - - - - - - DISTANCE=4681 rs2501105 1:225231117 G 127602 NM_001373.1 Transcript intron_variant - - - - - - rs2449326 1:225250934 C 127602 NM_001373.1 Transcript intron_variant - - - - - - rs3102111 1:225260412 G 127602 NM_001373.1 Transcript intron_variant - - - - - - rs3120983 1:225275162 A 127602 NM_001373.1 Transcript intron_variant - - - - - - rs1934204 1:225309753 G ENSESTG00000020040 ENSESTT00000050214 Transcript downstream_gene_variant - - - - - - DISTANCE=2593 rs1934204 1:225309753 G 127602 NM_001373.1 Transcript intron_variant - - - - - - rs12143049 1:225348599 A 127602 NM_001373.1 Transcript intron_variant - - - - - - rs10753403 1:225557809 T 127602 NM_001373.1 Transcript intron_variant - - - - - - rs10799305 1:225591893 T ENSESTG00000004194 ENSESTT00000010621 Transcript intron_variant - - - - - - rs10799305 1:225591893 T ENSESTG00000003887 ENSESTT00000009808 Transcript downstream_gene_variant - - - - - - DISTANCE=4906 rs10799305 1:225591893 T ENSESTG00000003887 ENSESTT00000009807 Transcript downstream_gene_variant - - - - - - DISTANCE=4906 rs10799305 1:225591893 T 3930 NM_002296.3 Transcript intron_variant - - - - - - rs10799305 1:225591893 T CCDS1545.1 CCDS1545.1 Transcript intron_variant - - - - - - rs10799305 1:225591893 T ENSESTG00000004194 ENSESTT00000010624 Transcript intron_variant - - - - - - rs10799305 1:225591893 T ENSESTG00000004194 ENSESTT00000010629 Transcript downstream_gene_variant - - - - - - DISTANCE=212 rs10799305 1:225591893 T 127602 NM_001373.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4897 rs10799305 1:225591893 T 3930 NM_194442.2 Transcript intron_variant - - - - - - rs2639713 1:225852627 A ENSESTG00000004153 ENSESTT00000010488 Transcript upstream_gene_variant - - - - - - DISTANCE=3249 rs11806236 1:225972217 C ENSESTG00000003907 ENSESTT00000009911 Transcript intron_variant - - - - - - rs11806236 1:225972217 C ENSESTG00000003907 ENSESTT00000009975 Transcript intron_variant - - - - - - rs11806236 1:225972217 C ENSESTG00000003907 ENSESTT00000009890 Transcript intron_variant - - - - - - rs11806236 1:225972217 C 6726 NM_003133.5 Transcript intron_variant - - - - - - rs11806236 1:225972217 C 6726 NM_001130440.1 Transcript intron_variant - - - - - - rs11806236 1:225972217 C ENSESTG00000003907 ENSESTT00000009961 Transcript intron_variant - - - - - - rs11806236 1:225972217 C ENSESTG00000003907 ENSESTT00000009905 Transcript intron_variant - - - - - - rs11806236 1:225972217 C CCDS1546.1 CCDS1546.1 Transcript intron_variant - - - - - - rs11806236 1:225972217 C CCDS44323.1 CCDS44323.1 Transcript intron_variant - - - - - - rs2854457 1:226011543 G ENSESTG00000003953 ENSESTT00000010055 Transcript intron_variant - - - - - - rs2854457 1:226011543 G CCDS1547.1 CCDS1547.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4888 rs2854457 1:226011543 G ENSESTG00000003953 ENSESTT00000010072 Transcript upstream_gene_variant - - - - - - DISTANCE=1459 rs2854457 1:226011543 G ENSESTG00000003953 ENSESTT00000010024 Transcript intron_variant - - - - - - rs2854457 1:226011543 G ENSESTG00000003953 ENSESTT00000010062 Transcript intron_variant - - - - - - rs2854457 1:226011543 G 2052 NM_000120.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1459 rs2854457 1:226011543 G 2052 NM_001136018.2 Transcript intron_variant - - - - - - rs2854457 1:226011543 G ENSESTG00000003953 ENSESTT00000010070 Transcript upstream_gene_variant - - - - - - DISTANCE=1459 rs10799336 1:226269480 C - - - intergenic_variant - - - - - - rs2666857 1:226322648 C - - - intergenic_variant - - - - - - rs3008188 1:226329676 A 64746 NM_022735.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2704 rs3008188 1:226329676 A CCDS1551.1 CCDS1551.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4635 rs3008185 1:226369417 T 64746 NM_022735.3 Transcript intron_variant - - - - - - rs3008185 1:226369417 T ENSESTG00000025040 ENSESTT00000063218 Transcript intron_variant - - - - - - rs3008185 1:226369417 T CCDS1551.1 CCDS1551.1 Transcript intron_variant - - - - - - rs3008184 1:226369752 G - ENSR00001529515 RegulatoryFeature regulatory_region_variant - - - - - - rs3008184 1:226369752 G 64746 NM_022735.3 Transcript intron_variant - - - - - - rs3008184 1:226369752 G ENSESTG00000025040 ENSESTT00000063218 Transcript intron_variant - - - - - - rs3008184 1:226369752 G ENSESTG00000023920 ENSESTT00000060352 Transcript upstream_gene_variant - - - - - - DISTANCE=4781 rs3008184 1:226369752 G CCDS1551.1 CCDS1551.1 Transcript intron_variant - - - - - - rs3008183 1:226371436 T 64746 NM_022735.3 Transcript intron_variant - - - - - - rs3008183 1:226371436 T ENSESTG00000025040 ENSESTT00000063218 Transcript intron_variant - - - - - - rs3008183 1:226371436 T ENSESTG00000023920 ENSESTT00000060352 Transcript upstream_gene_variant - - - - - - DISTANCE=3097 rs3008183 1:226371436 T CCDS1551.1 CCDS1551.1 Transcript intron_variant - - - - - - rs6605033 1:226429731 A 286826 NM_001270410.1 Transcript intron_variant - - - - - - rs6605033 1:226429731 A 286826 NM_001270409.1 Transcript intron_variant - - - - - - rs6605033 1:226429731 A CCDS1553.1 CCDS1553.1 Transcript intron_variant - - - - - - rs6605033 1:226429731 A 286826 NM_173083.3 Transcript intron_variant - - - - - - rs4653724 1:226517468 G - - - intergenic_variant - - - - - - rs1832789 1:226528100 C - - - intergenic_variant - - - - - - rs2793656 1:226624979 G - ENSR00000554207 RegulatoryFeature regulatory_region_variant - - - - - - rs2793656 1:226624979 G - - - intergenic_variant - - - - - - rs2614941 1:226806558 G - - - intergenic_variant - - - - - - rs2376853 1:227007278 C - - - intergenic_variant - - - - - - rs3134878 1:227099277 A - - - intergenic_variant - - - - - - rs4233222 1:227461469 A - ENSR00001529602 RegulatoryFeature regulatory_region_variant - - - - - - rs4233222 1:227461469 A 8476 NM_014826.4 Transcript intron_variant - - - - - - rs4233222 1:227461469 A 8476 NM_003607.3 Transcript intron_variant - - - - - - rs4233222 1:227461469 A CCDS1558.1 CCDS1558.1 Transcript intron_variant - - - - - - rs4233222 1:227461469 A ENSESTG00000018904 ENSESTT00000047581 Transcript intron_variant - - - - - - rs4233222 1:227461469 A CCDS1559.1 CCDS1559.1 Transcript intron_variant - - - - - - rs2402083 1:227933785 A ENSESTG00000018613 ENSESTT00000046968 Transcript intron_variant - - - - - - rs2402083 1:227933785 A ENSESTG00000018613 ENSESTT00000046943 Transcript intron_variant - - - - - - rs2402083 1:227933785 A ENSESTG00000018835 ENSESTT00000047406 Transcript upstream_gene_variant - - - - - - DISTANCE=94 rs2402083 1:227933785 A CCDS1562.1 CCDS1562.1 Transcript intron_variant - - - - - - rs2402083 1:227933785 A ENSESTG00000018613 ENSESTT00000046955 Transcript intron_variant - - - - - - rs2402083 1:227933785 A ENSESTG00000018613 ENSESTT00000046971 Transcript intron_variant - - - - - - rs2402083 1:227933785 A ENSESTG00000018613 ENSESTT00000046986 Transcript intron_variant - - - - - - rs2402083 1:227933785 A 116841 NM_053052.3 Transcript intron_variant - - - - - - rs2402083 1:227933785 A ENSESTG00000018613 ENSESTT00000046953 Transcript intron_variant - - - - - - rs2402083 1:227933785 A ENSESTG00000018613 ENSESTT00000046989 Transcript intron_variant - - - - - - rs2402083 1:227933785 A ENSESTG00000018613 ENSESTT00000046935 Transcript intron_variant - - - - - - rs173298 1:228916266 C - - - intergenic_variant - - - - - - rs381721 1:229307146 G ENSESTG00000025598 ENSESTT00000064543 Transcript intron_variant - - - - - - rs385641 1:229353212 T - - - intergenic_variant - - - - - - rs237796 1:229457208 A 126731 NM_145257.3 Transcript 3_prime_UTR_variant 4665 - - - - - rs237796 1:229457208 A ENSESTG00000008631 ENSESTT00000021688 Transcript downstream_gene_variant - - - - - - DISTANCE=1795 rs237796 1:229457208 A ENSESTG00000008623 ENSESTT00000021681 Transcript downstream_gene_variant - - - - - - DISTANCE=3301 rs237796 1:229457208 A CCDS1577.1 CCDS1577.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3774 rs2683459 1:230043143 C - - - intergenic_variant - - - - - - rs4492633 1:230854020 T ENSESTG00000034458 ENSESTT00000087172 Transcript upstream_gene_variant - - - - - - DISTANCE=4152 rs4492633 1:230854020 T 183 NM_000029.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3684 rs6688281 1:231086752 G ENSESTG00000034397 ENSESTT00000087098 Transcript intron_variant - - - - - - rs6688281 1:231086752 G ENSESTG00000034397 ENSESTT00000087107 Transcript intron_variant - - - - - - rs6688281 1:231086752 G ENSESTG00000034397 ENSESTT00000087101 Transcript intron_variant - - - - - - rs6688281 1:231086752 G 79573 NM_024525.4 Transcript intron_variant - - - - - - rs6688281 1:231086752 G ENSESTG00000034397 ENSESTT00000087092 Transcript intron_variant - - - - - - rs6688281 1:231086752 G ENSESTG00000034397 ENSESTT00000087084 Transcript intron_variant - - - - - - rs6688281 1:231086752 G 79573 NM_001122835.2 Transcript intron_variant - - - - - - rs6688281 1:231086752 G ENSESTG00000034397 ENSESTT00000087086 Transcript intron_variant - - - - - - rs6688281 1:231086752 G ENSESTG00000034397 ENSESTT00000087094 Transcript intron_variant - - - - - - rs6688281 1:231086752 G CCDS1588.1 CCDS1588.1 Transcript intron_variant - - - - - - rs6688281 1:231086752 G CCDS44332.2 CCDS44332.2 Transcript intron_variant - - - - - - rs6688281 1:231086752 G ENSESTG00000034397 ENSESTT00000087102 Transcript intron_variant - - - - - - rs6688281 1:231086752 G ENSESTG00000034397 ENSESTT00000087109 Transcript intron_variant - - - - - - rs6693752 1:231323140 A 149373 NM_001256615.1 Transcript intron_variant - - - - - - rs6693752 1:231323140 A 440730 NM_001004342.3 Transcript intron_variant - - - - - - rs6693752 1:231323140 A ENSESTG00000034381 ENSESTT00000086951 Transcript intron_variant - - - - - - rs6693752 1:231323140 A CCDS44333.1 CCDS44333.1 Transcript intron_variant - - - - - - rs4658903 1:231347412 G - ENSR00000554831 RegulatoryFeature regulatory_region_variant - - - - - - rs4658903 1:231347412 G ENSESTG00000023739 ENSESTT00000059843 Transcript intron_variant - - - - - - rs4658903 1:231347412 G 440730 NM_001004342.3 Transcript intron_variant - - - - - - rs4658903 1:231347412 G CCDS44333.1 CCDS44333.1 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060194 Transcript intron_variant - - - - - - rs556132 1:231382272 G CCDS1592.1 CCDS1592.1 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060179 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060495 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060235 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060350 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060516 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060361 Transcript intron_variant - - - - - - rs556132 1:231382272 G 8443 NM_014236.3 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060507 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060343 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060319 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060499 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060438 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060324 Transcript intron_variant - - - - - - rs556132 1:231382272 G ENSESTG00000023761 ENSESTT00000060314 Transcript intron_variant - - - - - - rs4658952 1:231972383 G - ENSR00001529971 RegulatoryFeature regulatory_region_variant - - - - - - rs4658952 1:231972383 G CCDS31055.1 CCDS31055.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G CCDS53485.1 CCDS53485.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001164539.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001164547.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 100303453 NR_028393.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001012959.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G CCDS53483.1 CCDS53483.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001164546.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G CCDS53482.1 CCDS53482.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G ENSESTG00000024141 ENSESTT00000061001 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001164537.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_018662.2 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001164541.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001164540.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001012957.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001164542.1 Transcript intron_variant - - - - - - rs4658952 1:231972383 G 27185 NM_001164538.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A 27185 NM_001164546.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A 27185 NM_001164541.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A 27185 NM_018662.2 Transcript intron_variant - - - - - - rs701159 1:232089047 A 27185 NM_001164537.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A CCDS53485.1 CCDS53485.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A 27185 NM_001164547.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A 27185 NM_001164540.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A 27185 NM_001012957.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A 27185 NM_001164538.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A 27185 NM_001164542.1 Transcript intron_variant - - - - - - rs701159 1:232089047 A 100303453 NR_028393.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs701159 1:232089047 A CCDS53483.1 CCDS53483.1 Transcript intron_variant - - - - - - rs10752759 1:233560013 T - - - intergenic_variant - - - - - - rs677816 1:234372434 A ENSESTG00000012983 ENSESTT00000032566 Transcript intron_variant - - - - - - rs677816 1:234372434 A CCDS1600.1 CCDS1600.1 Transcript intron_variant - - - - - - rs677816 1:234372434 A 148641 NM_173508.2 Transcript intron_variant - - - - - - rs677816 1:234372434 A ENSESTG00000033065 ENSESTT00000083561 Transcript intron_variant - - - - - - rs9804088 1:234386513 T ENSESTG00000012983 ENSESTT00000032566 Transcript intron_variant - - - - - - rs9804088 1:234386513 T CCDS1600.1 CCDS1600.1 Transcript intron_variant - - - - - - rs9804088 1:234386513 T 148641 NM_173508.2 Transcript intron_variant - - - - - - rs9804088 1:234386513 T ENSESTG00000033065 ENSESTT00000083561 Transcript intron_variant - - - - - - rs613512 1:234433533 A ENSESTG00000012983 ENSESTT00000032566 Transcript intron_variant - - - - - - rs613512 1:234433533 A CCDS1600.1 CCDS1600.1 Transcript intron_variant - - - - - - rs613512 1:234433533 A 148641 NM_173508.2 Transcript intron_variant - - - - - - rs613512 1:234433533 A ENSESTG00000033065 ENSESTT00000083561 Transcript intron_variant - - - - - - rs271768 1:234675287 A - ENSR00001530200 RegulatoryFeature regulatory_region_variant - - - - - - rs271768 1:234675287 A - - - intergenic_variant - - - - - - rs1329127 1:234736933 C - ENSR00000672558 RegulatoryFeature regulatory_region_variant - - - - - - rs1329127 1:234736933 C 359948 NM_001077397.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3082 rs1329127 1:234736933 C 359948 NM_182972.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3082 rs7533659 1:234737788 A - ENSR00000555274 RegulatoryFeature regulatory_region_variant - - - - - - rs7533659 1:234737788 A 359948 NM_001077397.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2227 rs7533659 1:234737788 A 359948 NM_182972.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2227 rs6673063 1:235076357 T - - - intergenic_variant - - - - - - rs4589167 1:235284582 A CCDS1603.1 CCDS1603.1 Transcript intron_variant - - - - - - rs4589167 1:235284582 A ENSESTG00000033159 ENSESTT00000083819 Transcript intron_variant - - - - - - rs4589167 1:235284582 A ENSESTG00000033159 ENSESTT00000083812 Transcript intron_variant - - - - - - rs4589167 1:235284582 A 9804 NM_014765.2 Transcript intron_variant - - - - - - rs10925285 1:235432729 G ENSESTG00000001903 ENSESTT00000004722 Transcript intron_variant - - - - - - rs10925285 1:235432729 G ENSESTG00000001903 ENSESTT00000004768 Transcript intron_variant - - - - - - rs10925285 1:235432729 G CCDS31061.1 CCDS31061.1 Transcript intron_variant - - - - - - rs10925285 1:235432729 G 51742 NM_016374.5 Transcript intron_variant - - - - - - rs10925285 1:235432729 G ENSESTG00000001903 ENSESTT00000004769 Transcript intron_variant - - - - - - rs10925285 1:235432729 G 51742 NM_031371.3 Transcript intron_variant - - - - - - rs10925285 1:235432729 G 51742 NM_001206794.1 Transcript intron_variant - - - - - - rs10925285 1:235432729 G CCDS31060.1 CCDS31060.1 Transcript intron_variant - - - - - - rs10925285 1:235432729 G ENSESTG00000001903 ENSESTT00000004756 Transcript intron_variant - - - - - - rs10925285 1:235432729 G ENSESTG00000001903 ENSESTT00000004770 Transcript intron_variant - - - - - - rs2891014 1:235438183 T ENSESTG00000001903 ENSESTT00000004722 Transcript intron_variant - - - - - - rs2891014 1:235438183 T ENSESTG00000001903 ENSESTT00000004768 Transcript intron_variant - - - - - - rs2891014 1:235438183 T CCDS31061.1 CCDS31061.1 Transcript intron_variant - - - - - - rs2891014 1:235438183 T 51742 NM_016374.5 Transcript intron_variant - - - - - - rs2891014 1:235438183 T ENSESTG00000001903 ENSESTT00000004769 Transcript intron_variant - - - - - - rs2891014 1:235438183 T 51742 NM_031371.3 Transcript intron_variant - - - - - - rs2891014 1:235438183 T 51742 NM_001206794.1 Transcript intron_variant - - - - - - rs2891014 1:235438183 T CCDS31060.1 CCDS31060.1 Transcript intron_variant - - - - - - rs2891014 1:235438183 T ENSESTG00000001903 ENSESTT00000004756 Transcript intron_variant - - - - - - rs2891014 1:235438183 T ENSESTG00000001903 ENSESTT00000004770 Transcript intron_variant - - - - - - rs2789368 1:235504807 T CCDS1604.1 CCDS1604.1 Transcript intron_variant - - - - - - rs2789368 1:235504807 T ENSESTG00000001725 ENSESTT00000004228 Transcript intron_variant - - - - - - rs2789368 1:235504807 T 9453 NR_036605.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2789368 1:235504807 T 9453 NM_001037277.1 Transcript intron_variant - - - - - - rs2789368 1:235504807 T ENSESTG00000001711 ENSESTT00000004222 Transcript intron_variant - - - - - - rs2789368 1:235504807 T ENSESTG00000001711 ENSESTT00000004213 Transcript intron_variant - - - - - - rs291382 1:235642185 C 148789 NM_152490.2 Transcript intron_variant - - - - - - rs291382 1:235642185 C ENSESTG00000001864 ENSESTT00000004674 Transcript intron_variant - - - - - - rs291382 1:235642185 C ENSESTG00000001864 ENSESTT00000004676 Transcript intron_variant - - - - - - rs291382 1:235642185 C ENSESTG00000001864 ENSESTT00000004675 Transcript intron_variant - - - - - - rs291382 1:235642185 C CCDS1606.1 CCDS1606.1 Transcript intron_variant - - - - - - rs291382 1:235642185 C ENSESTG00000001864 ENSESTT00000004670 Transcript intron_variant - - - - - - rs4439350 1:235837291 T - ENSR00000555477 RegulatoryFeature regulatory_region_variant - - - - - - rs4439350 1:235837291 T ENSESTG00000001842 ENSESTT00000004550 Transcript intron_variant - - - - - - rs4439350 1:235837291 T CCDS31062.1 CCDS31062.1 Transcript intron_variant - - - - - - rs4439350 1:235837291 T 1130 NM_000081.2 Transcript intron_variant - - - - - - rs4233482 1:235845338 G ENSESTG00000001842 ENSESTT00000004550 Transcript upstream_gene_variant - - - - - - DISTANCE=4424 rs4233482 1:235845338 G CCDS31062.1 CCDS31062.1 Transcript intron_variant - - - - - - rs4233482 1:235845338 G 1130 NM_000081.2 Transcript intron_variant - - - - - - rs2799443 1:235961243 C CCDS31062.1 CCDS31062.1 Transcript intron_variant - - - - - - rs2799443 1:235961243 C 1130 NM_000081.2 Transcript intron_variant - - - - - - rs586997 1:236547425 T - - - intergenic_variant - - - - - - rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060081 Transcript intron_variant - - - - - - rs819430 1:236699285 C CCDS1611.1 CCDS1611.1 Transcript intron_variant - - - - - - rs819430 1:236699285 C 3964 NM_201544.2 Transcript intron_variant - - - - - - rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060095 Transcript intron_variant - - - - - - rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060087 Transcript intron_variant - - - - - - rs819430 1:236699285 C 3964 NM_006499.4 Transcript intron_variant - - - - - - rs819430 1:236699285 C CCDS1612.1 CCDS1612.1 Transcript intron_variant - - - - - - rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060113 Transcript intron_variant - - - - - - rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060133 Transcript intron_variant - - - - - - rs819430 1:236699285 C 3964 NM_201543.2 Transcript intron_variant - - - - - - rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060058 Transcript intron_variant - - - - - - rs819430 1:236699285 C 3964 NM_201545.2 Transcript intron_variant - - - - - - rs819430 1:236699285 C ENSESTG00000024501 ENSESTT00000061922 Transcript downstream_gene_variant - - - - - - DISTANCE=4113 rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060175 Transcript upstream_gene_variant - - - - - - DISTANCE=4574 rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060151 Transcript intron_variant - - - - - - rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060140 Transcript intron_variant - - - - - - rs819430 1:236699285 C ENSESTG00000023779 ENSESTT00000060078 Transcript intron_variant - - - - - - rs819431 1:236721731 C ENSESTG00000024382 ENSESTT00000061758 Transcript intron_variant - - - - - - rs819431 1:236721731 C ENSESTG00000024382 ENSESTT00000061772 Transcript synonymous_variant 1308 1269 423 A gcA/gcG - rs819431 1:236721731 C 55127 NM_018072.5 Transcript synonymous_variant 5162 5010 1670 A gcA/gcG - rs819431 1:236721731 C CCDS31066.1 CCDS31066.1 Transcript synonymous_variant 5010 5010 1670 A gcA/gcG - rs819431 1:236721731 C ENSESTG00000024382 ENSESTT00000061907 Transcript upstream_gene_variant - - - - - - DISTANCE=158 rs819432 1:236722182 T ENSESTG00000024382 ENSESTT00000061758 Transcript intron_variant - - - - - - rs819432 1:236722182 T ENSESTG00000024382 ENSESTT00000061772 Transcript intron_variant - - - - - - rs819432 1:236722182 T 55127 NM_018072.5 Transcript intron_variant - - - - - - rs819432 1:236722182 T CCDS31066.1 CCDS31066.1 Transcript intron_variant - - - - - - rs819432 1:236722182 T ENSESTG00000024382 ENSESTT00000061907 Transcript upstream_gene_variant - - - - - - DISTANCE=609 rs707218 1:236854970 A CCDS1613.1 CCDS1613.1 Transcript intron_variant - - - - - - rs707218 1:236854970 A ENSESTG00000023896 ENSESTT00000060731 Transcript intron_variant - - - - - - rs707218 1:236854970 A ENSESTG00000023896 ENSESTT00000060593 Transcript intron_variant - - - - - - rs707218 1:236854970 A ENSESTG00000023896 ENSESTT00000060763 Transcript intron_variant - - - - - - rs707218 1:236854970 A ENSESTG00000023896 ENSESTT00000060632 Transcript intron_variant - - - - - - rs707218 1:236854970 A ENSESTG00000023896 ENSESTT00000060713 Transcript intron_variant - - - - - - rs707218 1:236854970 A 88 NM_001103.2 Transcript intron_variant - - - - - - rs707218 1:236854970 A ENSESTG00000023896 ENSESTT00000060720 Transcript intron_variant - - - - - - rs707218 1:236854970 A ENSESTG00000023896 ENSESTT00000060742 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060801 Transcript intron_variant - - - - - - rs707212 1:236870246 T CCDS1613.1 CCDS1613.1 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060811 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060731 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060593 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060808 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060763 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060632 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060713 Transcript intron_variant - - - - - - rs707212 1:236870246 T 88 NM_001103.2 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060720 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060742 Transcript intron_variant - - - - - - rs707212 1:236870246 T ENSESTG00000023896 ENSESTT00000060787 Transcript intron_variant - - - - - - rs707203 1:236897633 G - ENSR00000555624 RegulatoryFeature regulatory_region_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060822 Transcript 5_prime_UTR_variant 442 - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060801 Transcript intron_variant - - - - - - rs707203 1:236897633 G CCDS1613.1 CCDS1613.1 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060811 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060731 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060593 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060808 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060763 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060632 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060713 Transcript intron_variant - - - - - - rs707203 1:236897633 G 88 NM_001103.2 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060720 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060742 Transcript intron_variant - - - - - - rs707203 1:236897633 G ENSESTG00000023896 ENSESTT00000060787 Transcript intron_variant - - - - - - rs1252254 1:237007523 G CCDS1614.1 CCDS1614.1 Transcript intron_variant - - - - - - rs1252254 1:237007523 G ENSESTG00000024103 ENSESTT00000061299 Transcript intron_variant - - - - - - rs1252254 1:237007523 G ENSESTG00000024103 ENSESTT00000061310 Transcript intron_variant - - - - - - rs1252254 1:237007523 G 4548 NM_000254.2 Transcript intron_variant - - - - - - rs2791956 1:237011845 C CCDS1614.1 CCDS1614.1 Transcript intron_variant - - - - - - rs2791956 1:237011845 C ENSESTG00000024103 ENSESTT00000061299 Transcript intron_variant - - - - - - rs2791956 1:237011845 C ENSESTG00000024103 ENSESTT00000061310 Transcript intron_variant - - - - - - rs2791956 1:237011845 C 4548 NM_000254.2 Transcript intron_variant - - - - - - rs1770584 1:237030672 G CCDS1614.1 CCDS1614.1 Transcript intron_variant - - - - - - rs1770584 1:237030672 G ENSESTG00000024103 ENSESTT00000061299 Transcript intron_variant - - - - - - rs1770584 1:237030672 G ENSESTG00000024103 ENSESTT00000061310 Transcript intron_variant - - - - - - rs1770584 1:237030672 G 4548 NM_000254.2 Transcript intron_variant - - - - - - rs2712831 1:237037853 A CCDS1614.1 CCDS1614.1 Transcript intron_variant - - - - - - rs2712831 1:237037853 A ENSESTG00000024103 ENSESTT00000061299 Transcript intron_variant - - - - - - rs2712831 1:237037853 A ENSESTG00000024103 ENSESTT00000061310 Transcript intron_variant - - - - - - rs2712831 1:237037853 A 4548 NM_000254.2 Transcript intron_variant - - - - - - rs946938 1:237071069 A 4548 NM_000254.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3788 rs597924 1:237379669 C CCDS55691.1 CCDS55691.1 Transcript intron_variant - - - - - - rs597924 1:237379669 C 6262 NM_001035.2 Transcript intron_variant - - - - - - rs10925425 1:237630809 A CCDS55691.1 CCDS55691.1 Transcript intron_variant - - - - - - rs10925425 1:237630809 A 6262 NM_001035.2 Transcript intron_variant - - - - - - rs10925425 1:237630809 A 100616141 NR_039626.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3610 rs2779366 1:237695666 G CCDS55691.1 CCDS55691.1 Transcript intron_variant - - - - - - rs2779366 1:237695666 G 6262 NM_001035.2 Transcript intron_variant - - - - - - rs1464462 1:237921676 T ENSESTG00000010087 ENSESTT00000025275 Transcript upstream_gene_variant - - - - - - DISTANCE=1390 rs1464462 1:237921676 T ENSESTG00000010087 ENSESTT00000025263 Transcript intron_variant - - - - - - rs1464462 1:237921676 T CCDS55691.1 CCDS55691.1 Transcript intron_variant - - - - - - rs1464462 1:237921676 T ENSESTG00000010087 ENSESTT00000025253 Transcript intron_variant - - - - - - rs1464462 1:237921676 T 6262 NM_001035.2 Transcript intron_variant - - - - - - rs1464462 1:237921676 T ENSESTG00000010193 ENSESTT00000025463 Transcript intron_variant - - - - - - rs2247621 1:238280959 T ENSESTG00000010131 ENSESTT00000025342 Transcript intron_variant - - - - - - rs496806 1:238377180 A - - - intergenic_variant - - - - - - rs543237 1:238701706 T - - - intergenic_variant - - - - - - rs646136 1:238702913 G - - - intergenic_variant - - - - - - rs7532254 1:238906422 C - - - intergenic_variant - - - - - - rs1509696 1:239216564 T ENSESTG00000015894 ENSESTT00000039861 Transcript upstream_gene_variant - - - - - - DISTANCE=389 rs10737837 1:239738461 A - - - intergenic_variant - - - - - - rs10802796 1:239872728 A ENSESTG00000016092 ENSESTT00000040343 Transcript intron_variant - - - - - - rs10802796 1:239872728 A 1131 NM_000740.2 Transcript intron_variant - - - - - - rs589264 1:240031380 C ENSESTG00000016092 ENSESTT00000040358 Transcript intron_variant - - - - - - rs589264 1:240031380 C ENSESTG00000016092 ENSESTT00000040343 Transcript intron_variant - - - - - - rs589264 1:240031380 C ENSESTG00000016092 ENSESTT00000040354 Transcript intron_variant - - - - - - rs589264 1:240031380 C 1131 NM_000740.2 Transcript intron_variant - - - - - - rs6689742 1:240493636 C ENSESTG00000022480 ENSESTT00000056955 Transcript intron_variant - - - - - - rs6689742 1:240493636 C ENSESTG00000022480 ENSESTT00000056947 Transcript intron_variant - - - - - - rs6689742 1:240493636 C ENSESTG00000022480 ENSESTT00000056929 Transcript intron_variant - - - - - - rs6689742 1:240493636 C ENSESTG00000022480 ENSESTT00000056777 Transcript downstream_gene_variant - - - - - - DISTANCE=1240 rs6689742 1:240493636 C 56776 NM_020066.4 Transcript intron_variant - - - - - - rs6689742 1:240493636 C CCDS31069.2 CCDS31069.2 Transcript intron_variant - - - - - - rs10926242 1:240567343 C ENSESTG00000022480 ENSESTT00000056955 Transcript intron_variant - - - - - - rs10926242 1:240567343 C ENSESTG00000022480 ENSESTT00000056947 Transcript intron_variant - - - - - - rs10926242 1:240567343 C ENSESTG00000022480 ENSESTT00000056929 Transcript intron_variant - - - - - - rs10926242 1:240567343 C 56776 NM_020066.4 Transcript intron_variant - - - - - - rs10926242 1:240567343 C CCDS31069.2 CCDS31069.2 Transcript intron_variant - - - - - - rs10754716 1:240916015 T - - - intergenic_variant - - - - - - rs6659205 1:240935203 A ENSESTG00000022596 ENSESTT00000057265 Transcript downstream_gene_variant - - - - - - DISTANCE=3688 rs6659205 1:240935203 A 6000 NM_002924.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3614 rs6659205 1:240935203 A CCDS31071.1 CCDS31071.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4260 rs1342448 1:240938266 G ENSESTG00000022596 ENSESTT00000057265 Transcript downstream_gene_variant - - - - - - DISTANCE=625 rs1342448 1:240938266 G 6000 NM_002924.4 Transcript downstream_gene_variant - - - - - - DISTANCE=551 rs1342448 1:240938266 G CCDS31071.1 CCDS31071.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1197 rs2502444 1:241086670 G 6000 NM_002924.4 Transcript intron_variant - - - - - - rs2502444 1:241086670 G ENSESTG00000022596 ENSESTT00000057220 Transcript intron_variant - - - - - - rs2502444 1:241086670 G ENSESTG00000022596 ENSESTT00000057160 Transcript intron_variant - - - - - - rs2502444 1:241086670 G ENSESTG00000022596 ENSESTT00000057155 Transcript intron_variant - - - - - - rs2502444 1:241086670 G ENSESTG00000022596 ENSESTT00000057209 Transcript intron_variant - - - - - - rs2502444 1:241086670 G ENSESTG00000022596 ENSESTT00000057215 Transcript intron_variant - - - - - - rs2502444 1:241086670 G ENSESTG00000022596 ENSESTT00000057228 Transcript intron_variant - - - - - - rs2502444 1:241086670 G CCDS31071.1 CCDS31071.1 Transcript intron_variant - - - - - - rs2502444 1:241086670 G ENSESTG00000022596 ENSESTT00000057245 Transcript intron_variant - - - - - - rs2255114 1:241121379 G 6000 NM_002924.4 Transcript intron_variant - - - - - - rs2255114 1:241121379 G ENSESTG00000022596 ENSESTT00000057220 Transcript intron_variant - - - - - - rs2255114 1:241121379 G ENSESTG00000022596 ENSESTT00000057160 Transcript intron_variant - - - - - - rs2255114 1:241121379 G ENSESTG00000022596 ENSESTT00000057155 Transcript intron_variant - - - - - - rs2255114 1:241121379 G ENSESTG00000022596 ENSESTT00000057209 Transcript intron_variant - - - - - - rs2255114 1:241121379 G ENSESTG00000022596 ENSESTT00000057215 Transcript intron_variant - - - - - - rs2255114 1:241121379 G ENSESTG00000022596 ENSESTT00000057228 Transcript intron_variant - - - - - - rs2255114 1:241121379 G CCDS31071.1 CCDS31071.1 Transcript intron_variant - - - - - - rs2255114 1:241121379 G ENSESTG00000022596 ENSESTT00000057245 Transcript intron_variant - - - - - - rs261855 1:241124560 G 6000 NM_002924.4 Transcript intron_variant - - - - - - rs261855 1:241124560 G ENSESTG00000022596 ENSESTT00000057220 Transcript intron_variant - - - - - - rs261855 1:241124560 G ENSESTG00000022596 ENSESTT00000057160 Transcript intron_variant - - - - - - rs261855 1:241124560 G ENSESTG00000022596 ENSESTT00000057155 Transcript intron_variant - - - - - - rs261855 1:241124560 G ENSESTG00000022596 ENSESTT00000057209 Transcript intron_variant - - - - - - rs261855 1:241124560 G ENSESTG00000022596 ENSESTT00000057215 Transcript intron_variant - - - - - - rs261855 1:241124560 G ENSESTG00000022596 ENSESTT00000057228 Transcript intron_variant - - - - - - rs261855 1:241124560 G CCDS31071.1 CCDS31071.1 Transcript intron_variant - - - - - - rs261855 1:241124560 G ENSESTG00000022596 ENSESTT00000057245 Transcript intron_variant - - - - - - rs2678777 1:241240425 T 6000 NM_002924.4 Transcript intron_variant - - - - - - rs2678777 1:241240425 T ENSESTG00000022596 ENSESTT00000057220 Transcript intron_variant - - - - - - rs2678777 1:241240425 T ENSESTG00000022596 ENSESTT00000057160 Transcript intron_variant - - - - - - rs2678777 1:241240425 T ENSESTG00000022596 ENSESTT00000057155 Transcript intron_variant - - - - - - rs2678777 1:241240425 T ENSESTG00000022596 ENSESTT00000057209 Transcript intron_variant - - - - - - rs2678777 1:241240425 T ENSESTG00000022596 ENSESTT00000057215 Transcript intron_variant - - - - - - rs2678777 1:241240425 T ENSESTG00000022596 ENSESTT00000057228 Transcript intron_variant - - - - - - rs2678777 1:241240425 T CCDS31071.1 CCDS31071.1 Transcript intron_variant - - - - - - rs636731 1:241787644 G 1122 NM_001821.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4522 rs636731 1:241787644 G ENSESTG00000034095 ENSESTT00000086200 Transcript intron_variant - - - - - - rs636731 1:241787644 G ENSESTG00000034095 ENSESTT00000086193 Transcript intron_variant - - - - - - rs636731 1:241787644 G CCDS31072.1 CCDS31072.1 Transcript intron_variant - - - - - - rs636731 1:241787644 G 23596 NM_014322.2 Transcript intron_variant - - - - - - rs3121388 1:242020261 G 9156 NM_003686.4 Transcript intron_variant - - - - - - rs3121388 1:242020261 G ENSESTG00000034057 ENSESTT00000086124 Transcript intron_variant - - - - - - rs3121388 1:242020261 G ENSESTG00000034057 ENSESTT00000086113 Transcript intron_variant - - - - - - rs3121388 1:242020261 G ENSESTG00000034057 ENSESTT00000086118 Transcript intron_variant - - - - - - rs3121388 1:242020261 G 9156 NM_006027.4 Transcript intron_variant - - - - - - rs3121388 1:242020261 G 9156 NM_130398.3 Transcript intron_variant - - - - - - rs3121388 1:242020261 G CCDS44336.1 CCDS44336.1 Transcript intron_variant - - - - - - rs3121388 1:242020261 G CCDS1620.1 CCDS1620.1 Transcript intron_variant - - - - - - rs28441562 1:242157214 T 440738 NM_001004343.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1578 rs28441562 1:242157214 T CCDS31074.1 CCDS31074.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2251 rs28499272 1:242163040 G 440738 NM_001004343.2 Transcript upstream_gene_variant - - - - - - DISTANCE=655 rs28499272 1:242163040 G CCDS31074.1 CCDS31074.1 Transcript upstream_gene_variant - - - - - - DISTANCE=730 rs28477554 1:242173275 G - - - intergenic_variant - - - - - - rs2340300 1:242175271 G - ENSR00001530641 RegulatoryFeature regulatory_region_variant - - - - - - rs2340300 1:242175271 G - - - intergenic_variant - - - - - - rs10737880 1:242549821 C ENSESTG00000017726 ENSESTT00000044732 Transcript intron_variant - - - - - - rs10737880 1:242549821 C ENSESTG00000017726 ENSESTT00000044685 Transcript intron_variant - - - - - - rs10737880 1:242549821 C CCDS1621.2 CCDS1621.2 Transcript intron_variant - - - - - - rs10737880 1:242549821 C 200150 NM_152666.2 Transcript intron_variant - - - - - - rs10737880 1:242549821 C CCDS55692.1 CCDS55692.1 Transcript intron_variant - - - - - - rs10737880 1:242549821 C 200150 NM_001195812.1 Transcript intron_variant - - - - - - rs10737880 1:242549821 C 200150 NM_001195811.1 Transcript intron_variant - - - - - - rs10737880 1:242549821 C ENSESTG00000017726 ENSESTT00000044710 Transcript intron_variant - - - - - - rs2491866 1:243036552 T - - - intergenic_variant - - - - - - rs2502314 1:243088016 T - ENSR00000290462 RegulatoryFeature regulatory_region_variant - - - - - - rs2502314 1:243088016 T - - - intergenic_variant - - - - - - rs3013410 1:243146755 A - - - intergenic_variant - - - - - - rs2932628 1:243414002 A 9859 NM_014812.2 Transcript intron_variant - - - - - - rs2932628 1:243414002 A 9859 NM_001042404.1 Transcript intron_variant - - - - - - rs2932628 1:243414002 A 9859 NM_001042405.1 Transcript intron_variant - - - - - - rs2932628 1:243414002 A ENSESTG00000016946 ENSESTT00000042660 Transcript intron_variant - - - - - - rs2932628 1:243414002 A ENSESTG00000016946 ENSESTT00000042666 Transcript intron_variant - - - - - - rs2932628 1:243414002 A ENSESTG00000016752 ENSESTT00000042192 Transcript upstream_gene_variant - - - - - - DISTANCE=4486 rs2932628 1:243414002 A ENSESTG00000016752 ENSESTT00000042169 Transcript upstream_gene_variant - - - - - - DISTANCE=4486 rs2932628 1:243414002 A ENSESTG00000016752 ENSESTT00000042165 Transcript upstream_gene_variant - - - - - - DISTANCE=4486 rs2932628 1:243414002 A ENSESTG00000016946 ENSESTT00000042650 Transcript intron_variant - - - - - - rs2932628 1:243414002 A ENSESTG00000016752 ENSESTT00000042156 Transcript upstream_gene_variant - - - - - - DISTANCE=4486 rs2932628 1:243414002 A ENSESTG00000016752 ENSESTT00000042139 Transcript upstream_gene_variant - - - - - - DISTANCE=4486 rs2932628 1:243414002 A ENSESTG00000016752 ENSESTT00000042176 Transcript upstream_gene_variant - - - - - - DISTANCE=4486 rs320327 1:243801283 C ENSESTG00000016862 ENSESTT00000042480 Transcript intron_variant - - - - - - rs320327 1:243801283 C 10000 NM_001206729.1 Transcript intron_variant - - - - - - rs320327 1:243801283 C CCDS31076.1 CCDS31076.1 Transcript intron_variant - - - - - - rs320327 1:243801283 C CCDS31077.1 CCDS31077.1 Transcript intron_variant - - - - - - rs320327 1:243801283 C ENSESTG00000016862 ENSESTT00000042452 Transcript intron_variant - - - - - - rs320327 1:243801283 C ENSESTG00000016862 ENSESTT00000042428 Transcript intron_variant - - - - - - rs320327 1:243801283 C ENSESTG00000016862 ENSESTT00000042468 Transcript intron_variant - - - - - - rs320327 1:243801283 C ENSESTG00000016862 ENSESTT00000042448 Transcript intron_variant - - - - - - rs320327 1:243801283 C 10000 NM_181690.2 Transcript intron_variant - - - - - - rs320327 1:243801283 C ENSESTG00000016862 ENSESTT00000042464 Transcript intron_variant - - - - - - rs320327 1:243801283 C ENSESTG00000016862 ENSESTT00000042461 Transcript intron_variant - - - - - - rs320327 1:243801283 C 10000 NM_005465.4 Transcript intron_variant - - - - - - rs320327 1:243801283 C ENSESTG00000016862 ENSESTT00000042447 Transcript intron_variant - - - - - - rs6429434 1:243903069 C ENSESTG00000016862 ENSESTT00000042480 Transcript intron_variant - - - - - - rs6429434 1:243903069 C 10000 NM_001206729.1 Transcript intron_variant - - - - - - rs6429434 1:243903069 C CCDS31076.1 CCDS31076.1 Transcript intron_variant - - - - - - rs6429434 1:243903069 C CCDS31077.1 CCDS31077.1 Transcript intron_variant - - - - - - rs6429434 1:243903069 C ENSESTG00000016862 ENSESTT00000042452 Transcript intron_variant - - - - - - rs6429434 1:243903069 C ENSESTG00000016862 ENSESTT00000042428 Transcript intron_variant - - - - - - rs6429434 1:243903069 C ENSESTG00000016862 ENSESTT00000042468 Transcript intron_variant - - - - - - rs6429434 1:243903069 C ENSESTG00000016862 ENSESTT00000042448 Transcript intron_variant - - - - - - rs6429434 1:243903069 C 10000 NM_181690.2 Transcript intron_variant - - - - - - rs6429434 1:243903069 C ENSESTG00000016862 ENSESTT00000042464 Transcript intron_variant - - - - - - rs6429434 1:243903069 C ENSESTG00000016862 ENSESTT00000042461 Transcript intron_variant - - - - - - rs6429434 1:243903069 C 10000 NM_005465.4 Transcript intron_variant - - - - - - rs6429434 1:243903069 C ENSESTG00000016862 ENSESTT00000042447 Transcript intron_variant - - - - - - rs10803165 1:244015175 T ENSESTG00000016862 ENSESTT00000042452 Transcript upstream_gene_variant - - - - - - DISTANCE=794 rs10803165 1:244015175 T ENSESTG00000016862 ENSESTT00000042428 Transcript upstream_gene_variant - - - - - - DISTANCE=794 rs10803165 1:244015175 T ENSESTG00000016862 ENSESTT00000042448 Transcript upstream_gene_variant - - - - - - DISTANCE=794 rs10803165 1:244015175 T ENSESTG00000016862 ENSESTT00000042447 Transcript upstream_gene_variant - - - - - - DISTANCE=794 rs2675919 1:244081424 C - ENSR00001038287 RegulatoryFeature regulatory_region_variant - - - - - - rs2675919 1:244081424 C 339529 NR_033883.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs543161 1:244171236 C 339529 NR_033883.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs506304 1:244177531 G 339529 NR_033883.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs496258 1:244181512 C 339529 NR_033883.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2486534 1:244192008 C 339529 NR_033883.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2453202 1:244197328 G 339529 NR_033883.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2486536 1:244219563 G CCDS1622.1 CCDS1622.1 Transcript downstream_gene_variant - - - - - - DISTANCE=891 rs2486536 1:244219563 G 10472 NM_205768.2 Transcript 3_prime_UTR_variant 2660 - - - - - rs2486536 1:244219563 G 10472 NM_006352.3 Transcript 3_prime_UTR_variant 2982 - - - - - rs2486536 1:244219563 G ENSESTG00000016838 ENSESTT00000042298 Transcript downstream_gene_variant - - - - - - DISTANCE=2043 rs2486536 1:244219563 G ENSESTG00000016838 ENSESTT00000042291 Transcript downstream_gene_variant - - - - - - DISTANCE=2097 rs2486539 1:244233155 T - - - intergenic_variant - - - - - - rs2500498 1:244265725 T ENSESTG00000003975 ENSESTT00000010051 Transcript upstream_gene_variant - - - - - - DISTANCE=4942 rs1890180 1:245335485 A CCDS44342.1 CCDS44342.1 Transcript intron_variant - - - - - - rs1890180 1:245335485 A 55083 NM_018012.3 Transcript intron_variant - - - - - - rs4658720 1:245351034 G CCDS44342.1 CCDS44342.1 Transcript intron_variant - - - - - - rs4658720 1:245351034 G 55083 NM_018012.3 Transcript intron_variant - - - - - - rs7554774 1:245360427 G CCDS44342.1 CCDS44342.1 Transcript intron_variant - - - - - - rs7554774 1:245360427 G 55083 NM_018012.3 Transcript intron_variant - - - - - - rs7554789 1:245360484 G CCDS44342.1 CCDS44342.1 Transcript intron_variant - - - - - - rs7554789 1:245360484 G 55083 NM_018012.3 Transcript intron_variant - - - - - - rs7554902 1:245360565 G CCDS44342.1 CCDS44342.1 Transcript intron_variant - - - - - - rs7554902 1:245360565 G 55083 NM_018012.3 Transcript intron_variant - - - - - - rs6676934 1:245483056 G CCDS44342.1 CCDS44342.1 Transcript intron_variant - - - - - - rs6676934 1:245483056 G 55083 NM_018012.3 Transcript intron_variant - - - - - - rs9287179 1:246015859 C CCDS31083.1 CCDS31083.1 Transcript intron_variant - - - - - - rs9287179 1:246015859 C ENSESTG00000034797 ENSESTT00000087984 Transcript intron_variant - - - - - - rs9287179 1:246015859 C 64754 NM_001167740.1 Transcript intron_variant - - - - - - rs9287179 1:246015859 C CCDS53486.1 CCDS53486.1 Transcript intron_variant - - - - - - rs9287179 1:246015859 C ENSESTG00000034797 ENSESTT00000087986 Transcript intron_variant - - - - - - rs9287179 1:246015859 C 64754 NM_022743.2 Transcript intron_variant - - - - - - rs7528961 1:246207048 T - ENSR00000556464 RegulatoryFeature regulatory_region_variant - - - - - - rs7528961 1:246207048 T CCDS31083.1 CCDS31083.1 Transcript intron_variant - - - - - - rs7528961 1:246207048 T ENSESTG00000034797 ENSESTT00000087984 Transcript intron_variant - - - - - - rs7528961 1:246207048 T 64754 NM_001167740.1 Transcript intron_variant - - - - - - rs7528961 1:246207048 T CCDS53486.1 CCDS53486.1 Transcript intron_variant - - - - - - rs7528961 1:246207048 T 64754 NM_022743.2 Transcript intron_variant - - - - - - rs7522856 1:246360565 G CCDS31083.1 CCDS31083.1 Transcript intron_variant - - - - - - rs7522856 1:246360565 G 64754 NM_001167740.1 Transcript intron_variant - - - - - - rs7522856 1:246360565 G CCDS53486.1 CCDS53486.1 Transcript intron_variant - - - - - - rs7522856 1:246360565 G 64754 NM_022743.2 Transcript intron_variant - - - - - - rs1148708 1:246460890 C - ENSR00000556492 RegulatoryFeature regulatory_region_variant - - - - - - rs1148708 1:246460890 C CCDS31083.1 CCDS31083.1 Transcript intron_variant - - - - - - rs1148708 1:246460890 C 64754 NM_001167740.1 Transcript intron_variant - - - - - - rs1148708 1:246460890 C CCDS53486.1 CCDS53486.1 Transcript intron_variant - - - - - - rs1148708 1:246460890 C 64754 NM_022743.2 Transcript intron_variant - - - - - - rs4654238 1:246502949 G CCDS31083.1 CCDS31083.1 Transcript intron_variant - - - - - - rs4654238 1:246502949 G ENSESTG00000026463 ENSESTT00000066721 Transcript intron_variant - - - - - - rs4654238 1:246502949 G ENSESTG00000026463 ENSESTT00000066705 Transcript intron_variant - - - - - - rs4654238 1:246502949 G 64754 NM_001167740.1 Transcript intron_variant - - - - - - rs4654238 1:246502949 G CCDS53486.1 CCDS53486.1 Transcript intron_variant - - - - - - rs4654238 1:246502949 G 64754 NM_022743.2 Transcript intron_variant - - - - - - rs1890160 1:246712033 G ENSESTG00000026399 ENSESTT00000066634 Transcript intron_variant - - - - - - rs1890160 1:246712033 G CCDS1627.1 CCDS1627.1 Transcript intron_variant - - - - - - rs1890160 1:246712033 G 64216 NM_022366.2 Transcript intron_variant - - - - - - rs3124071 1:246720798 A ENSESTG00000026399 ENSESTT00000066634 Transcript synonymous_variant 540 441 147 I atC/atT - rs3124071 1:246720798 A CCDS1627.1 CCDS1627.1 Transcript synonymous_variant 441 441 147 I atC/atT - rs3124071 1:246720798 A 64216 NM_022366.2 Transcript synonymous_variant 566 441 147 I atC/atT - rs3124071 1:246720798 A ENSESTG00000026399 ENSESTT00000066513 Transcript intron_variant - - - - - - rs2341681 1:246723869 T ENSESTG00000026399 ENSESTT00000066634 Transcript intron_variant - - - - - - rs2341681 1:246723869 T CCDS1627.1 CCDS1627.1 Transcript intron_variant - - - - - - rs2341681 1:246723869 T 64216 NM_022366.2 Transcript intron_variant - - - - - - rs2341681 1:246723869 T ENSESTG00000026399 ENSESTT00000066513 Transcript intron_variant - - - - - - rs10737798 1:247367342 A 100500849 NR_037480.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1980 rs10737798 1:247367342 A ENSESTG00000000717 ENSESTT00000001710 Transcript intron_variant - - - - - - rs10737798 1:247367342 A ENSESTG00000000717 ENSESTT00000001708 Transcript intron_variant - - - - - - rs10737798 1:247367342 A ENSESTG00000000720 ENSESTT00000001723 Transcript upstream_gene_variant - - - - - - DISTANCE=3845 rs1175749 1:247969966 T - - - intergenic_variant - - - - - - rs7550351 1:248139526 G 284521 NM_175911.2 Transcript intron_variant - - - - - - rs7550351 1:248139526 G ENSESTG00000000687 ENSESTT00000001654 Transcript intron_variant - - - - - - rs4528149 1:248165208 A 284521 NM_175911.2 Transcript intron_variant - - - - - - rs4528149 1:248165208 A ENSESTG00000000687 ENSESTT00000001654 Transcript intron_variant - - - - - - rs2211001 1:248171988 C 284521 NM_175911.2 Transcript intron_variant - - - - - - rs2211001 1:248171988 C ENSESTG00000000687 ENSESTT00000001654 Transcript intron_variant - - - - - - rs7531446 1:248228639 T 391192 NM_001004687.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3717 rs7531446 1:248228639 T 284521 NM_175911.2 Transcript intron_variant - - - - - - rs7531446 1:248228639 T ENSESTG00000000687 ENSESTT00000001654 Transcript intron_variant - - - - - - rs7531446 1:248228639 T CCDS31104.1 CCDS31104.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3717 rs7537913 1:248513413 T CCDS31112.1 CCDS31112.1 Transcript downstream_gene_variant - - - - - - DISTANCE=398 rs7537913 1:248513413 T 127066 NM_001001918.1 Transcript downstream_gene_variant - - - - - - DISTANCE=398 rs4501918 10:455212 C ENSESTG00000002978 ENSESTT00000007429 Transcript downstream_gene_variant - - - - - - DISTANCE=4763 rs4501918 10:455212 C 22982 NM_014974.2 Transcript intron_variant - - - - - - rs4501918 10:455212 C CCDS7054.1 CCDS7054.1 Transcript intron_variant - - - - - - rs1250892 10:1013018 C - - - intergenic_variant - - - - - - rs7915678 10:1073166 G 55853 NR_024629.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7915678 10:1073166 G ENSESTG00000011972 ENSESTT00000030026 Transcript intron_variant - - - - - - rs7915678 10:1073166 G 91734 NM_033261.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1367 rs7915678 10:1073166 G 55853 NR_027709.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7915678 10:1073166 G ENSESTG00000011972 ENSESTT00000030028 Transcript intron_variant - - - - - - rs7915678 10:1073166 G 55853 NR_024628.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7915678 10:1073166 G ENSESTG00000011972 ENSESTT00000030024 Transcript intron_variant - - - - - - rs7915678 10:1073166 G ENSESTG00000011972 ENSESTT00000030016 Transcript downstream_gene_variant - - - - - - DISTANCE=80 rs7915678 10:1073166 G CCDS7055.1 CCDS7055.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2503 rs7915678 10:1073166 G 55853 NR_027708.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1909435 10:1747573 G CCDS7058.1 CCDS7058.1 Transcript intron_variant - - - - - - rs1909435 10:1747573 G 105 NM_018702.3 Transcript intron_variant - - - - - - rs10903624 10:2048966 G 282980 NR_040253.1 Transcript non_coding_exon_variant,nc_transcript_variant 798 - - - - - rs1333205 10:2224896 T ENSESTG00000000936 ENSESTT00000002244 Transcript intron_variant - - - - - - rs1333205 10:2224896 T ENSESTG00000000936 ENSESTT00000002240 Transcript intron_variant - - - - - - rs2765678 10:2415171 C ENSESTG00000000927 ENSESTT00000002218 Transcript intron_variant - - - - - - rs7097027 10:2478181 C ENSESTG00000000927 ENSESTT00000002218 Transcript intron_variant - - - - - - rs4881011 10:2729982 G - - - intergenic_variant - - - - - - rs1981095 10:2737546 C - - - intergenic_variant - - - - - - rs7078506 10:3011993 T - - - intergenic_variant - - - - - - rs7088894 10:3063470 G - - - intergenic_variant - - - - - - rs2388585 10:3071155 G - - - intergenic_variant - - - - - - rs10903947 10:3096194 C - - - intergenic_variant - - - - - - rs10903950 10:3098037 G - - - intergenic_variant - - - - - - rs12571307 10:3128104 G 5214 NM_001242339.1 Transcript intron_variant - - - - - - rs12571307 10:3128104 G ENSESTG00000033692 ENSESTT00000085176 Transcript intron_variant - - - - - - rs12571307 10:3128104 G CCDS55698.1 CCDS55698.1 Transcript intron_variant - - - - - - rs12571307 10:3128104 G ENSESTG00000033692 ENSESTT00000085218 Transcript intron_variant - - - - - - rs12571307 10:3128104 G ENSESTG00000033692 ENSESTT00000085204 Transcript intron_variant - - - - - - rs12571307 10:3128104 G ENSESTG00000033692 ENSESTT00000085186 Transcript intron_variant - - - - - - rs12571307 10:3128104 G ENSESTG00000033692 ENSESTT00000085163 Transcript intron_variant - - - - - - rs12571307 10:3128104 G ENSESTG00000033692 ENSESTT00000085195 Transcript intron_variant - - - - - - rs12571307 10:3128104 G 5214 NM_002627.4 Transcript intron_variant - - - - - - rs12571307 10:3128104 G CCDS7059.1 CCDS7059.1 Transcript intron_variant - - - - - - rs10751913 10:3132520 G 5214 NM_001242339.1 Transcript intron_variant - - - - - - rs10751913 10:3132520 G ENSESTG00000033692 ENSESTT00000085176 Transcript intron_variant - - - - - - rs10751913 10:3132520 G CCDS55698.1 CCDS55698.1 Transcript intron_variant - - - - - - rs10751913 10:3132520 G ENSESTG00000033692 ENSESTT00000085218 Transcript intron_variant - - - - - - rs10751913 10:3132520 G ENSESTG00000033692 ENSESTT00000085204 Transcript intron_variant - - - - - - rs10751913 10:3132520 G ENSESTG00000033692 ENSESTT00000085186 Transcript intron_variant - - - - - - rs10751913 10:3132520 G ENSESTG00000033692 ENSESTT00000085163 Transcript intron_variant - - - - - - rs10751913 10:3132520 G ENSESTG00000033692 ENSESTT00000085195 Transcript intron_variant - - - - - - rs10751913 10:3132520 G 5214 NM_002627.4 Transcript intron_variant - - - - - - rs10751913 10:3132520 G CCDS7059.1 CCDS7059.1 Transcript intron_variant - - - - - - rs4881080 10:3143643 C 5214 NM_001242339.1 Transcript synonymous_variant 551 327 109 R cgA/cgC - rs4881080 10:3143643 C ENSESTG00000033692 ENSESTT00000085176 Transcript synonymous_variant 399 351 117 R cgA/cgC - rs4881080 10:3143643 C CCDS55698.1 CCDS55698.1 Transcript synonymous_variant 327 327 109 R cgA/cgC - rs4881080 10:3143643 C ENSESTG00000033692 ENSESTT00000085218 Transcript synonymous_variant 396 237 79 R cgA/cgC - rs4881080 10:3143643 C ENSESTG00000033692 ENSESTT00000085204 Transcript synonymous_variant 440 247 83 R Agg/Cgg - rs4881080 10:3143643 C ENSESTG00000033692 ENSESTT00000085186 Transcript downstream_gene_variant - - - - - - DISTANCE=482 rs4881080 10:3143643 C ENSESTG00000033692 ENSESTT00000085163 Transcript synonymous_variant 329 237 79 R cgA/cgC - rs4881080 10:3143643 C ENSESTG00000033692 ENSESTT00000085195 Transcript downstream_gene_variant - - - - - - DISTANCE=9 rs4881080 10:3143643 C 5214 NM_002627.4 Transcript synonymous_variant 427 351 117 R cgA/cgC - rs4881080 10:3143643 C ENSESTG00000033738 ENSESTT00000085312 Transcript upstream_gene_variant - - - - - - DISTANCE=3400 rs4881080 10:3143643 C CCDS7059.1 CCDS7059.1 Transcript synonymous_variant 351 351 117 R cgA/cgC - rs11251718 10:3144526 G 5214 NM_001242339.1 Transcript intron_variant - - - - - - rs11251718 10:3144526 G ENSESTG00000033692 ENSESTT00000085176 Transcript intron_variant - - - - - - rs11251718 10:3144526 G CCDS55698.1 CCDS55698.1 Transcript intron_variant - - - - - - rs11251718 10:3144526 G ENSESTG00000033692 ENSESTT00000085218 Transcript intron_variant - - - - - - rs11251718 10:3144526 G ENSESTG00000033692 ENSESTT00000085204 Transcript downstream_gene_variant - - - - - - DISTANCE=776 rs11251718 10:3144526 G ENSESTG00000033692 ENSESTT00000085186 Transcript downstream_gene_variant - - - - - - DISTANCE=1365 rs11251718 10:3144526 G ENSESTG00000033692 ENSESTT00000085163 Transcript intron_variant - - - - - - rs11251718 10:3144526 G ENSESTG00000033692 ENSESTT00000085195 Transcript downstream_gene_variant - - - - - - DISTANCE=892 rs11251718 10:3144526 G 5214 NM_002627.4 Transcript intron_variant - - - - - - rs11251718 10:3144526 G ENSESTG00000033738 ENSESTT00000085312 Transcript upstream_gene_variant - - - - - - DISTANCE=2517 rs11251718 10:3144526 G CCDS7059.1 CCDS7059.1 Transcript intron_variant - - - - - - rs10795006 10:3152741 A - ENSR00001420438 RegulatoryFeature regulatory_region_variant - - - - - - rs10795006 10:3152741 A ENSESTG00000033738 ENSESTT00000085419 Transcript intron_variant - - - - - - rs10795006 10:3152741 A ENSESTG00000033738 ENSESTT00000085427 Transcript intron_variant - - - - - - rs10795006 10:3152741 A 5214 NM_001242339.1 Transcript intron_variant - - - - - - rs10795006 10:3152741 A ENSESTG00000033738 ENSESTT00000085416 Transcript intron_variant - - - - - - rs10795006 10:3152741 A CCDS55698.1 CCDS55698.1 Transcript intron_variant - - - - - - rs10795006 10:3152741 A ENSESTG00000033738 ENSESTT00000085429 Transcript intron_variant - - - - - - rs10795006 10:3152741 A ENSESTG00000033738 ENSESTT00000085424 Transcript intron_variant - - - - - - rs10795006 10:3152741 A ENSESTG00000033738 ENSESTT00000085418 Transcript intron_variant - - - - - - rs10795006 10:3152741 A 5214 NM_002627.4 Transcript intron_variant - - - - - - rs10795006 10:3152741 A CCDS7059.1 CCDS7059.1 Transcript intron_variant - - - - - - rs10795006 10:3152741 A ENSESTG00000033738 ENSESTT00000085312 Transcript downstream_gene_variant - - - - - - DISTANCE=1778 rs12413324 10:3333120 G - - - intergenic_variant - - - - - - rs505500 10:3368054 G - - - intergenic_variant - - - - - - rs705460 10:3616029 A ENSESTG00000033931 ENSESTT00000085751 Transcript intron_variant - - - - - - rs4391732 10:3854964 T - - - intergenic_variant - - - - - - rs10751955 10:4106355 G - - - intergenic_variant - - - - - - rs2397404 10:4143540 A - - - intergenic_variant - - - - - - rs10904198 10:4174656 C - - - intergenic_variant - - - - - - rs1926811 10:4397237 A - - - intergenic_variant - - - - - - rs4488101 10:4497468 A - - - intergenic_variant - - - - - - rs7089963 10:5145084 C ENSESTG00000018169 ENSESTT00000045899 Transcript intron_variant - - - - - - rs7089963 10:5145084 C 8644 NM_003739.5 Transcript intron_variant - - - - - - rs7089963 10:5145084 C 8644 NM_001253909.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4716 rs7089963 10:5145084 C ENSESTG00000018792 ENSESTT00000047363 Transcript intron_variant - - - - - - rs7089963 10:5145084 C 8644 NM_001253908.1 Transcript intron_variant - - - - - - rs7089963 10:5145084 C ENSESTG00000009332 ENSESTT00000023405 Transcript intron_variant - - - - - - rs7089963 10:5145084 C CCDS7063.1 CCDS7063.1 Transcript intron_variant - - - - - - rs1781942 10:5184085 G - - - intergenic_variant - - - - - - rs7914957 10:5534839 T - - - intergenic_variant - - - - - - rs7899662 10:5645161 A - - - intergenic_variant - - - - - - rs4747329 10:5649351 G - - - intergenic_variant - - - - - - rs7087479 10:6162844 G - ENSR00001420718 RegulatoryFeature regulatory_region_variant - - - - - - rs7087479 10:6162844 G 84991 NM_032905.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3422 rs7087479 10:6162844 G ENSESTG00000012574 ENSESTT00000031536 Transcript downstream_gene_variant - - - - - - DISTANCE=4770 rs7087479 10:6162844 G 84991 NM_001145547.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3422 rs7074211 10:6368724 T 399715 NR_040079.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1262876 10:6425365 C - ENSR00000350219 RegulatoryFeature regulatory_region_variant - - - - - - rs1262876 10:6425365 C - - - intergenic_variant - - - - - - rs641000 10:6515193 C ENSESTG00000012770 ENSESTT00000032046 Transcript intron_variant - - - - - - rs641000 10:6515193 C ENSESTG00000012770 ENSESTT00000032042 Transcript intron_variant - - - - - - rs641000 10:6515193 C CCDS55701.1 CCDS55701.1 Transcript intron_variant - - - - - - rs641000 10:6515193 C 5588 NM_006257.3 Transcript intron_variant - - - - - - rs641000 10:6515193 C CCDS7079.1 CCDS7079.1 Transcript intron_variant - - - - - - rs641000 10:6515193 C 5588 NM_001242413.1 Transcript intron_variant - - - - - - rs491839 10:6564181 G ENSESTG00000012728 ENSESTT00000031978 Transcript intron_variant - - - - - - rs491839 10:6564181 G 5588 NM_006257.3 Transcript intron_variant - - - - - - rs491839 10:6564181 G ENSESTG00000012728 ENSESTT00000031984 Transcript intron_variant - - - - - - rs491839 10:6564181 G 5588 NM_001242413.1 Transcript intron_variant - - - - - - rs7073635 10:6666534 G - - - intergenic_variant - - - - - - rs6602143 10:6742669 C - - - intergenic_variant - - - - - - rs2148957 10:6748698 G - - - intergenic_variant - - - - - - rs353215 10:6778555 T - - - intergenic_variant - - - - - - rs2486092 10:7006647 C - - - intergenic_variant - - - - - - rs3002158 10:7205266 G 57713 NM_001029880.2 Transcript 3_prime_UTR_variant 3344 - - - - - rs3002158 10:7205266 G CCDS31138.1 CCDS31138.1 Transcript downstream_gene_variant - - - - - - DISTANCE=466 rs3002158 10:7205266 G 57713 NM_001018039.1 Transcript 3_prime_UTR_variant 3242 - - - - - rs2497441 10:7209224 G 57713 NM_001029880.2 Transcript intron_variant - - - - - - rs2497441 10:7209224 G CCDS31138.1 CCDS31138.1 Transcript intron_variant - - - - - - rs2497441 10:7209224 G 57713 NM_001018039.1 Transcript intron_variant - - - - - - rs3002159 10:7246600 C 57713 NM_001029880.2 Transcript intron_variant - - - - - - rs3002159 10:7246600 C CCDS31138.1 CCDS31138.1 Transcript intron_variant - - - - - - rs3002159 10:7246600 C 57713 NM_001018039.1 Transcript intron_variant - - - - - - rs10752106 10:7362466 G 57713 NM_001029880.2 Transcript intron_variant - - - - - - rs10752106 10:7362466 G CCDS31138.1 CCDS31138.1 Transcript intron_variant - - - - - - rs10752106 10:7362466 G ENSESTG00000031053 ENSESTT00000078160 Transcript intron_variant - - - - - - rs10752106 10:7362466 G 57713 NM_001018039.1 Transcript intron_variant - - - - - - rs2247473 10:7493634 G - - - intergenic_variant - - - - - - rs10752121 10:7943978 G 83860 NM_031923.2 Transcript intron_variant - - - - - - rs10752121 10:7943978 G CCDS41487.1 CCDS41487.1 Transcript intron_variant - - - - - - rs10752121 10:7943978 G ENSESTG00000030975 ENSESTT00000077998 Transcript intron_variant - - - - - - rs1779651 10:8270340 C - - - intergenic_variant - - - - - - rs4307626 10:8751419 T - - - intergenic_variant - - - - - - rs1334545 10:8774862 C - - - intergenic_variant - - - - - - rs449603 10:8848308 T - - - intergenic_variant - - - - - - rs1149918 10:9175958 A - - - intergenic_variant - - - - - - rs1335242 10:9469155 T - - - intergenic_variant - - - - - - rs7893454 10:9962280 G - - - intergenic_variant - - - - - - rs4747871 10:10658360 A - - - intergenic_variant - - - - - - rs1473738 10:10913029 C - - - intergenic_variant - - - - - - rs201103 10:11029822 C - - - intergenic_variant - - - - - - rs6602545 10:11905214 A ENSESTG00000001882 ENSESTT00000004677 Transcript intron_variant - - - - - - rs6602545 10:11905214 A 219731 NR_038222.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6602545 10:11905214 A ENSESTG00000001877 ENSESTT00000004673 Transcript intron_variant - - - - - - rs6602545 10:11905214 A CCDS7085.1 CCDS7085.1 Transcript intron_variant - - - - - - rs6602545 10:11905214 A 254427 NM_153256.3 Transcript intron_variant - - - - - - rs6602545 10:11905214 A ENSESTG00000001877 ENSESTT00000004665 Transcript intron_variant - - - - - - rs2093915 10:11918018 G - ENSR00000350747 RegulatoryFeature regulatory_region_variant - - - - - - rs2093915 10:11918018 G 219731 NR_038222.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2093915 10:11918018 G 254427 NM_153256.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3742 rs7923942 10:11933218 C 219731 NR_038222.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4750140 10:11949175 C - ENSR00001421041 RegulatoryFeature regulatory_region_variant - - - - - - rs4750140 10:11949175 C - - - intergenic_variant - - - - - - rs6602569 10:12282828 G 8872 NM_006023.2 Transcript intron_variant - - - - - - rs6602569 10:12282828 G ENSESTG00000005853 ENSESTT00000014923 Transcript downstream_gene_variant - - - - - - DISTANCE=3650 rs6602569 10:12282828 G CCDS7090.1 CCDS7090.1 Transcript intron_variant - - - - - - rs6602569 10:12282828 G ENSESTG00000005853 ENSESTT00000014918 Transcript intron_variant - - - - - - rs6602569 10:12282828 G ENSESTG00000005853 ENSESTT00000014905 Transcript intron_variant - - - - - - rs7913305 10:12299757 T - - - intergenic_variant - - - - - - rs4747970 10:12302592 G - - - intergenic_variant - - - - - - rs7094023 10:12308438 G - - - intergenic_variant - - - - - - rs7073039 10:12308519 G - - - intergenic_variant - - - - - - rs7091116 10:12308913 G - - - intergenic_variant - - - - - - rs1320194 10:12316148 G - - - intergenic_variant - - - - - - rs7073790 10:12317168 T - - - intergenic_variant - - - - - - rs7084537 10:12319953 G - - - intergenic_variant - - - - - - rs2768349 10:12601920 A ENSESTG00000005910 ENSESTT00000014975 Transcript intron_variant - - - - - - rs2768349 10:12601920 A 57118 NM_153498.2 Transcript intron_variant - - - - - - rs2768349 10:12601920 A CCDS7091.1 CCDS7091.1 Transcript intron_variant - - - - - - rs2768349 10:12601920 A CCDS7092.1 CCDS7092.1 Transcript intron_variant - - - - - - rs2768349 10:12601920 A 57118 NM_020397.2 Transcript intron_variant - - - - - - rs2815619 10:12603735 C ENSESTG00000005910 ENSESTT00000014975 Transcript intron_variant - - - - - - rs2815619 10:12603735 C 57118 NM_153498.2 Transcript intron_variant - - - - - - rs2815619 10:12603735 C CCDS7091.1 CCDS7091.1 Transcript intron_variant - - - - - - rs2815619 10:12603735 C CCDS7092.1 CCDS7092.1 Transcript intron_variant - - - - - - rs2815619 10:12603735 C 57118 NM_020397.2 Transcript intron_variant - - - - - - rs6602597 10:12606439 A - ENSR00001421080 RegulatoryFeature regulatory_region_variant - - - - - - rs6602597 10:12606439 A ENSESTG00000005910 ENSESTT00000014975 Transcript intron_variant - - - - - - rs6602597 10:12606439 A 57118 NM_153498.2 Transcript intron_variant - - - - - - rs6602597 10:12606439 A CCDS7091.1 CCDS7091.1 Transcript intron_variant - - - - - - rs6602597 10:12606439 A CCDS7092.1 CCDS7092.1 Transcript intron_variant - - - - - - rs6602597 10:12606439 A 57118 NM_020397.2 Transcript intron_variant - - - - - - rs2482071 10:12881220 T 283070 NR_027322.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3675 rs2151991 10:13186271 G - ENSR00000350906 RegulatoryFeature regulatory_region_variant - - - - - - rs2151991 10:13186271 G - - - intergenic_variant - - - - - - rs7911975 10:13223408 G CCDS7095.1 CCDS7095.1 Transcript intron_variant - - - - - - rs7911975 10:13223408 G 55388 NM_182751.2 Transcript intron_variant - - - - - - rs7911975 10:13223408 G ENSESTG00000018664 ENSESTT00000047286 Transcript intron_variant - - - - - - rs7911975 10:13223408 G 55388 NM_018518.4 Transcript intron_variant - - - - - - rs7911975 10:13223408 G CCDS7096.1 CCDS7096.1 Transcript intron_variant - - - - - - rs7911975 10:13223408 G ENSESTG00000018664 ENSESTT00000047266 Transcript intron_variant - - - - - - rs7911975 10:13223408 G ENSESTG00000018664 ENSESTT00000047258 Transcript intron_variant - - - - - - rs2895564 10:13471408 A - - - intergenic_variant - - - - - - rs2478111 10:13635582 G - ENSR00001421164 RegulatoryFeature regulatory_region_variant - - - - - - rs2478111 10:13635582 G CCDS7100.1 CCDS7100.1 Transcript intron_variant - - - - - - rs2478111 10:13635582 G ENSESTG00000018989 ENSESTT00000047958 Transcript intron_variant - - - - - - rs2478111 10:13635582 G 8559 NM_003675.3 Transcript intron_variant - - - - - - rs7087064 10:13661907 T CCDS7100.1 CCDS7100.1 Transcript intron_variant - - - - - - rs7087064 10:13661907 T ENSESTG00000018989 ENSESTT00000047958 Transcript intron_variant - - - - - - rs7087064 10:13661907 T 8559 NM_003675.3 Transcript intron_variant - - - - - - rs1544303 10:13726794 G - ENSR00000350970 RegulatoryFeature regulatory_region_variant - - - - - - rs1544303 10:13726794 G ENSESTG00000019167 ENSESTT00000048239 Transcript intron_variant - - - - - - rs1544303 10:13726794 G ENSESTG00000019167 ENSESTT00000048273 Transcript intron_variant - - - - - - rs1544303 10:13726794 G ENSESTG00000019167 ENSESTT00000048204 Transcript intron_variant - - - - - - rs1544303 10:13726794 G 55691 NM_018027.3 Transcript intron_variant - - - - - - rs1544303 10:13726794 G ENSESTG00000019167 ENSESTT00000048284 Transcript intron_variant - - - - - - rs1544303 10:13726794 G CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs2049744 10:13815477 G 55691 NM_018027.3 Transcript intron_variant - - - - - - rs2049744 10:13815477 G CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs1539504 10:13874216 G - ENSR00000351015 RegulatoryFeature regulatory_region_variant - - - - - - rs1539504 10:13874216 G ENSESTG00000019240 ENSESTT00000048338 Transcript intron_variant - - - - - - rs1539504 10:13874216 G 55691 NM_018027.3 Transcript intron_variant - - - - - - rs1539504 10:13874216 G CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs1358586 10:13922190 G ENSESTG00000019240 ENSESTT00000048338 Transcript intron_variant - - - - - - rs1358586 10:13922190 G 55691 NM_018027.3 Transcript intron_variant - - - - - - rs1358586 10:13922190 G CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs2610802 10:13936070 C - ENSR00000351031 RegulatoryFeature regulatory_region_variant - - - - - - rs2610802 10:13936070 C ENSESTG00000019240 ENSESTT00000048338 Transcript intron_variant - - - - - - rs2610802 10:13936070 C 55691 NM_018027.3 Transcript intron_variant - - - - - - rs2610802 10:13936070 C CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs1881581 10:13961221 G - ENSR00000351037 RegulatoryFeature regulatory_region_variant - - - - - - rs1881581 10:13961221 G ENSESTG00000019240 ENSESTT00000048338 Transcript intron_variant - - - - - - rs1881581 10:13961221 G 55691 NM_018027.3 Transcript intron_variant - - - - - - rs1881581 10:13961221 G CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs2610816 10:13961973 A ENSESTG00000019240 ENSESTT00000048338 Transcript intron_variant - - - - - - rs2610816 10:13961973 A 55691 NM_018027.3 Transcript intron_variant - - - - - - rs2610816 10:13961973 A CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs2698117 10:13974875 A ENSESTG00000019240 ENSESTT00000048338 Transcript intron_variant - - - - - - rs2698117 10:13974875 A 55691 NM_018027.3 Transcript intron_variant - - - - - - rs2698117 10:13974875 A CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs2447028 10:14090479 G 55691 NM_018027.3 Transcript intron_variant - - - - - - rs2447028 10:14090479 G CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs4750465 10:14165864 G 55691 NM_018027.3 Transcript intron_variant - - - - - - rs4750465 10:14165864 G CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs9424187 10:14211042 A 55691 NM_018027.3 Transcript intron_variant - - - - - - rs9424187 10:14211042 A CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs4748091 10:14230117 A 55691 NM_018027.3 Transcript intron_variant - - - - - - rs4748091 10:14230117 A ENSESTG00000031780 ENSESTT00000080194 Transcript downstream_gene_variant - - - - - - DISTANCE=2831 rs4748091 10:14230117 A CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs6602714 10:14237383 A 55691 NM_018027.3 Transcript intron_variant - - - - - - rs6602714 10:14237383 A CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs1327009 10:14242707 A - ENSR00000642395 RegulatoryFeature regulatory_region_variant - - - - - - rs1327009 10:14242707 A 55691 NM_018027.3 Transcript intron_variant - - - - - - rs1327009 10:14242707 A CCDS7101.1 CCDS7101.1 Transcript intron_variant - - - - - - rs596559 10:14464850 C - - - intergenic_variant - - - - - - rs2148121 10:14553713 T - - - intergenic_variant - - - - - - rs7904796 10:14566534 G ENSESTG00000031960 ENSESTT00000080721 Transcript intron_variant - - - - - - rs7904796 10:14566534 G ENSESTG00000031960 ENSESTT00000080711 Transcript intron_variant - - - - - - rs7904796 10:14566534 G CCDS7102.1 CCDS7102.1 Transcript intron_variant - - - - - - rs7904796 10:14566534 G ENSESTG00000031960 ENSESTT00000080748 Transcript intron_variant - - - - - - rs7904796 10:14566534 G ENSESTG00000031960 ENSESTT00000080664 Transcript intron_variant - - - - - - rs7904796 10:14566534 G ENSESTG00000031960 ENSESTT00000080673 Transcript intron_variant - - - - - - rs7904796 10:14566534 G ENSESTG00000031960 ENSESTT00000080680 Transcript intron_variant - - - - - - rs7904796 10:14566534 G 83641 NM_031453.2 Transcript intron_variant - - - - - - rs7075309 10:14582148 C ENSESTG00000031960 ENSESTT00000080721 Transcript intron_variant - - - - - - rs7075309 10:14582148 C ENSESTG00000031960 ENSESTT00000080711 Transcript intron_variant - - - - - - rs7075309 10:14582148 C CCDS7102.1 CCDS7102.1 Transcript intron_variant - - - - - - rs7075309 10:14582148 C ENSESTG00000031960 ENSESTT00000080748 Transcript intron_variant - - - - - - rs7075309 10:14582148 C ENSESTG00000031960 ENSESTT00000080664 Transcript intron_variant - - - - - - rs7075309 10:14582148 C ENSESTG00000031960 ENSESTT00000080673 Transcript intron_variant - - - - - - rs7075309 10:14582148 C ENSESTG00000031960 ENSESTT00000080680 Transcript intron_variant - - - - - - rs7075309 10:14582148 C 83641 NM_031453.2 Transcript intron_variant - - - - - - rs10796206 10:14629187 G - ENSR00000351152 RegulatoryFeature regulatory_region_variant - - - - - - rs10796206 10:14629187 G CCDS7102.1 CCDS7102.1 Transcript intron_variant - - - - - - rs10796206 10:14629187 G ENSESTG00000031960 ENSESTT00000080680 Transcript intron_variant - - - - - - rs10796206 10:14629187 G ENSESTG00000031960 ENSESTT00000080664 Transcript intron_variant - - - - - - rs10796206 10:14629187 G ENSESTG00000031960 ENSESTT00000080673 Transcript intron_variant - - - - - - rs10796206 10:14629187 G 83641 NM_031453.2 Transcript intron_variant - - - - - - rs10796211 10:14678929 G CCDS7102.1 CCDS7102.1 Transcript intron_variant - - - - - - rs10796211 10:14678929 G 83641 NM_031453.2 Transcript intron_variant - - - - - - rs10906726 10:14682100 T CCDS7102.1 CCDS7102.1 Transcript intron_variant - - - - - - rs10906726 10:14682100 T 83641 NM_031453.2 Transcript intron_variant - - - - - - rs4750595 10:15132031 C 414149 NM_001039844.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1256 rs4750595 10:15132031 C CCDS31153.1 CCDS31153.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1304 rs4750595 10:15132031 C ENSESTG00000024605 ENSESTT00000062188 Transcript upstream_gene_variant - - - - - - DISTANCE=1256 rs4747255 10:16002201 C - - - intergenic_variant - - - - - - rs2354503 10:16008650 C - - - intergenic_variant - - - - - - rs780826 10:16888264 C CCDS7113.1 CCDS7113.1 Transcript intron_variant - - - - - - rs780826 10:16888264 C 8029 NM_001081.3 Transcript intron_variant - - - - - - rs780826 10:16888264 C ENSESTG00000007309 ENSESTT00000018422 Transcript intron_variant - - - - - - rs1907367 10:17124409 G CCDS7113.1 CCDS7113.1 Transcript intron_variant - - - - - - rs1907367 10:17124409 G 8029 NM_001081.3 Transcript intron_variant - - - - - - rs6602195 10:17495361 G - ENSR00000218961 RegulatoryFeature regulatory_region_variant - - - - - - rs6602195 10:17495361 G 338596 NM_001004470.1 Transcript intron_variant - - - - - - rs6602195 10:17495361 G ENSESTG00000020650 ENSESTT00000051784 Transcript downstream_gene_variant - - - - - - DISTANCE=4349 rs6602195 10:17495361 G CCDS31158.1 CCDS31158.1 Transcript intron_variant - - - - - - rs2489888 10:17612766 T - - - intergenic_variant - - - - - - rs10795501 10:17710769 T - ENSR00001421445 RegulatoryFeature regulatory_region_variant - - - - - - rs10795501 10:17710769 T ENSESTG00000020655 ENSESTT00000052059 Transcript intron_variant - - - - - - rs10795501 10:17710769 T CCDS7122.1 CCDS7122.1 Transcript intron_variant - - - - - - rs10795501 10:17710769 T 8027 NM_003473.3 Transcript intron_variant - - - - - - rs10795501 10:17710769 T ENSESTG00000020655 ENSESTT00000051969 Transcript intron_variant - - - - - - rs10795501 10:17710769 T 8027 NR_037774.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2497790 10:18329921 C CCDS7124.1 CCDS7124.1 Transcript intron_variant - - - - - - rs2497790 10:18329921 C 221074 NM_001145195.1 Transcript intron_variant - - - - - - rs2497790 10:18329921 C 221074 NM_152725.3 Transcript intron_variant - - - - - - rs2497790 10:18329921 C ENSESTG00000028851 ENSESTT00000072708 Transcript intron_variant - - - - - - rs2497790 10:18329921 C CCDS44362.1 CCDS44362.1 Transcript intron_variant - - - - - - rs4536107 10:18692361 A CCDS7129.1 CCDS7129.1 Transcript intron_variant - - - - - - rs4536107 10:18692361 A ENSESTG00000028912 ENSESTT00000072948 Transcript intron_variant - - - - - - rs4536107 10:18692361 A CCDS7126.1 CCDS7126.1 Transcript intron_variant - - - - - - rs4536107 10:18692361 A 783 NM_201596.2 Transcript intron_variant - - - - - - rs4536107 10:18692361 A 783 NM_001167945.1 Transcript intron_variant - - - - - - rs4536107 10:18692361 A ENSESTG00000028912 ENSESTT00000072980 Transcript downstream_gene_variant - - - - - - DISTANCE=1044 rs4536107 10:18692361 A 783 NM_201570.2 Transcript intron_variant - - - - - - rs4536107 10:18692361 A CCDS7127.1 CCDS7127.1 Transcript intron_variant - - - - - - rs4536107 10:18692361 A ENSESTG00000028912 ENSESTT00000072920 Transcript intron_variant - - - - - - rs4536107 10:18692361 A 783 NM_201572.3 Transcript intron_variant - - - - - - rs4536107 10:18692361 A 783 NM_201597.2 Transcript intron_variant - - - - - - rs4536107 10:18692361 A 783 NM_000724.3 Transcript intron_variant - - - - - - rs4536107 10:18692361 A ENSESTG00000028912 ENSESTT00000072868 Transcript intron_variant - - - - - - rs4536107 10:18692361 A ENSESTG00000028912 ENSESTT00000072897 Transcript downstream_gene_variant - - - - - - DISTANCE=1471 rs4536107 10:18692361 A 783 NM_201590.2 Transcript intron_variant - - - - - - rs4536107 10:18692361 A CCDS7128.1 CCDS7128.1 Transcript intron_variant - - - - - - rs4536107 10:18692361 A CCDS7125.1 CCDS7125.1 Transcript intron_variant - - - - - - rs4536107 10:18692361 A 783 NM_201571.3 Transcript intron_variant - - - - - - rs4536107 10:18692361 A CCDS41493.1 CCDS41493.1 Transcript intron_variant - - - - - - rs4536107 10:18692361 A ENSESTG00000028912 ENSESTT00000072908 Transcript intron_variant - - - - - - rs4536107 10:18692361 A CCDS41494.1 CCDS41494.1 Transcript intron_variant - - - - - - rs4536107 10:18692361 A 783 NM_201593.2 Transcript intron_variant - - - - - - rs4536107 10:18692361 A ENSESTG00000028912 ENSESTT00000072967 Transcript intron_variant - - - - - - rs2480342 10:19139307 T - - - intergenic_variant - - - - - - rs2813774 10:19368735 G - - - intergenic_variant - - - - - - rs2686649 10:19439070 C - - - intergenic_variant - - - - - - rs10740901 10:19753553 C ENSESTG00000003159 ENSESTT00000007843 Transcript intron_variant - - - - - - rs6482076 10:20303387 T ENSESTG00000031732 ENSESTT00000080198 Transcript intron_variant - - - - - - rs6482076 10:20303387 T CCDS7132.1 CCDS7132.1 Transcript intron_variant - - - - - - rs6482076 10:20303387 T ENSESTG00000031732 ENSESTT00000080215 Transcript intron_variant - - - - - - rs6482076 10:20303387 T ENSESTG00000031732 ENSESTT00000080230 Transcript intron_variant - - - - - - rs6482076 10:20303387 T 84898 NM_032812.7 Transcript intron_variant - - - - - - rs7076162 10:20576360 G - - - intergenic_variant - - - - - - rs6482111 10:20612257 A - - - intergenic_variant - - - - - - rs2496614 10:20755628 T - - - intergenic_variant - - - - - - rs10740979 10:20908657 A - - - intergenic_variant - - - - - - rs4748694 10:20981727 C - - - intergenic_variant - - - - - - rs1925526 10:21012142 T - - - intergenic_variant - - - - - - rs2574767 10:21081228 T CCDS7134.1 CCDS7134.1 Transcript intron_variant - - - - - - rs2574767 10:21081228 T ENSESTG00000024267 ENSESTT00000061472 Transcript intron_variant - - - - - - rs2574767 10:21081228 T ENSESTG00000024267 ENSESTT00000061422 Transcript intron_variant - - - - - - rs2574767 10:21081228 T 10529 NM_006393.2 Transcript intron_variant - - - - - - rs2574767 10:21081228 T 10529 NM_213569.2 Transcript intron_variant - - - - - - rs2574767 10:21081228 T 10529 NM_001173484.1 Transcript intron_variant - - - - - - rs2574767 10:21081228 T CCDS7133.1 CCDS7133.1 Transcript intron_variant - - - - - - rs2574767 10:21081228 T ENSESTG00000024267 ENSESTT00000061495 Transcript intron_variant - - - - - - rs2574767 10:21081228 T ENSESTG00000024267 ENSESTT00000061458 Transcript intron_variant - - - - - - rs654355 10:21319789 C ENSESTG00000024267 ENSESTT00000061422 Transcript intron_variant - - - - - - rs654355 10:21319789 C 10529 NM_213569.2 Transcript intron_variant - - - - - - rs654355 10:21319789 C 10529 NM_001173484.1 Transcript intron_variant - - - - - - rs654355 10:21319789 C CCDS7133.1 CCDS7133.1 Transcript intron_variant - - - - - - rs654355 10:21319789 C ENSESTG00000024267 ENSESTT00000061458 Transcript intron_variant - - - - - - rs4747432 10:21354035 C ENSESTG00000024267 ENSESTT00000061422 Transcript intron_variant - - - - - - rs4747432 10:21354035 C 10529 NM_213569.2 Transcript intron_variant - - - - - - rs4747432 10:21354035 C 10529 NM_001173484.1 Transcript intron_variant - - - - - - rs4747432 10:21354035 C CCDS7133.1 CCDS7133.1 Transcript intron_variant - - - - - - rs4747432 10:21354035 C ENSESTG00000024267 ENSESTT00000061458 Transcript intron_variant - - - - - - rs2788710 10:21943231 A 8028 NM_001195626.1 Transcript intron_variant - - - - - - rs2788710 10:21943231 A ENSESTG00000024176 ENSESTT00000061243 Transcript intron_variant - - - - - - rs2788710 10:21943231 A ENSESTG00000024176 ENSESTT00000061171 Transcript intron_variant - - - - - - rs2788710 10:21943231 A CCDS7135.1 CCDS7135.1 Transcript intron_variant - - - - - - rs2788710 10:21943231 A 8028 NM_004641.3 Transcript intron_variant - - - - - - rs2788710 10:21943231 A ENSESTG00000024176 ENSESTT00000061210 Transcript intron_variant - - - - - - rs2788710 10:21943231 A CCDS55708.1 CCDS55708.1 Transcript intron_variant - - - - - - rs1543564 10:23419004 G ENSESTG00000002929 ENSESTT00000007274 Transcript intron_variant - - - - - - rs6482367 10:24405338 A ENSESTG00000020921 ENSESTT00000052493 Transcript upstream_gene_variant - - - - - - DISTANCE=2124 rs6482367 10:24405338 A ENSESTG00000020921 ENSESTT00000052481 Transcript upstream_gene_variant - - - - - - DISTANCE=2119 rs6482367 10:24405338 A 56243 NM_001098500.1 Transcript intron_variant - - - - - - rs1326640 10:24467681 G ENSESTG00000020921 ENSESTT00000052493 Transcript intron_variant - - - - - - rs1326640 10:24467681 G 56243 NM_001098500.1 Transcript intron_variant - - - - - - rs7914983 10:24475280 T ENSESTG00000020921 ENSESTT00000052493 Transcript intron_variant - - - - - - rs7914983 10:24475280 T 56243 NM_001098500.1 Transcript intron_variant - - - - - - rs4748932 10:24526593 C 56243 NM_001098501.1 Transcript intron_variant - - - - - - rs4748932 10:24526593 C ENSESTG00000020921 ENSESTT00000052554 Transcript intron_variant - - - - - - rs4748932 10:24526593 C 56243 NM_019590.3 Transcript intron_variant - - - - - - rs4748932 10:24526593 C ENSESTG00000020921 ENSESTT00000052546 Transcript intron_variant - - - - - - rs4748932 10:24526593 C CCDS31165.1 CCDS31165.1 Transcript intron_variant - - - - - - rs4748932 10:24526593 C ENSESTG00000020921 ENSESTT00000052600 Transcript upstream_gene_variant - - - - - - DISTANCE=1428 rs4748932 10:24526593 C ENSESTG00000020921 ENSESTT00000052604 Transcript upstream_gene_variant - - - - - - DISTANCE=1546 rs4748932 10:24526593 C CCDS41496.1 CCDS41496.1 Transcript intron_variant - - - - - - rs4748932 10:24526593 C 56243 NM_001098500.1 Transcript intron_variant - - - - - - rs4748932 10:24526593 C ENSESTG00000020921 ENSESTT00000052586 Transcript upstream_gene_variant - - - - - - DISTANCE=1004 rs7086273 10:24752171 T - ENSR00001421859 RegulatoryFeature regulatory_region_variant - - - - - - rs7086273 10:24752171 T 56243 NM_001098501.1 Transcript intron_variant - - - - - - rs7086273 10:24752171 T 56243 NM_019590.3 Transcript intron_variant - - - - - - rs7086273 10:24752171 T CCDS31165.1 CCDS31165.1 Transcript intron_variant - - - - - - rs7086273 10:24752171 T ENSESTG00000020921 ENSESTT00000052600 Transcript intron_variant - - - - - - rs7086273 10:24752171 T ENSESTG00000020921 ENSESTT00000052604 Transcript intron_variant - - - - - - rs7086273 10:24752171 T CCDS41496.1 CCDS41496.1 Transcript intron_variant - - - - - - rs7086273 10:24752171 T ENSESTG00000020921 ENSESTT00000052626 Transcript intron_variant - - - - - - rs7086273 10:24752171 T 56243 NM_001098500.1 Transcript intron_variant - - - - - - rs7086273 10:24752171 T ENSESTG00000020921 ENSESTT00000052665 Transcript upstream_gene_variant - - - - - - DISTANCE=3263 rs7086273 10:24752171 T ENSESTG00000020921 ENSESTT00000052586 Transcript intron_variant - - - - - - rs2246236 10:24846039 T - ENSR00000352086 RegulatoryFeature regulatory_region_variant - - - - - - rs2246236 10:24846039 T - - - intergenic_variant - - - - - - rs10734053 10:24879281 G ENSESTG00000021087 ENSESTT00000052989 Transcript intron_variant - - - - - - rs10734053 10:24879281 G 57584 NM_020824.3 Transcript intron_variant - - - - - - rs10734053 10:24879281 G CCDS7144.2 CCDS7144.2 Transcript intron_variant - - - - - - rs10734053 10:24879281 G ENSESTG00000021173 ENSESTT00000053315 Transcript intron_variant - - - - - - rs10734053 10:24879281 G ENSESTG00000021173 ENSESTT00000053191 Transcript intron_variant - - - - - - rs8181350 10:24916696 G ENSESTG00000021087 ENSESTT00000052989 Transcript intron_variant - - - - - - rs8181350 10:24916696 G 57584 NM_020824.3 Transcript intron_variant - - - - - - rs8181350 10:24916696 G CCDS7144.2 CCDS7144.2 Transcript intron_variant - - - - - - rs8181350 10:24916696 G ENSESTG00000021087 ENSESTT00000052972 Transcript intron_variant - - - - - - rs10764524 10:25483933 A ENSESTG00000007455 ENSESTT00000018727 Transcript intron_variant - - - - - - rs10764524 10:25483933 A CCDS31166.1 CCDS31166.1 Transcript intron_variant - - - - - - rs10764524 10:25483933 A 57512 NM_020752.2 Transcript intron_variant - - - - - - rs2437410 10:26128669 C - - - intergenic_variant - - - - - - rs1889687 10:26667966 A - ENSR00000352217 RegulatoryFeature regulatory_region_variant - - - - - - rs1889687 10:26667966 A - - - intergenic_variant - - - - - - rs1197425 10:27026787 A - ENSR00000352269 RegulatoryFeature regulatory_region_variant - - - - - - rs1197425 10:27026787 A ENSESTG00000014905 ENSESTT00000037373 Transcript intron_variant - - - - - - rs1197425 10:27026787 A CCDS31168.1 CCDS31168.1 Transcript intron_variant - - - - - - rs1197425 10:27026787 A ENSESTG00000014905 ENSESTT00000037375 Transcript intron_variant - - - - - - rs1197425 10:27026787 A 23590 NM_014317.3 Transcript intron_variant - - - - - - rs1197425 10:27026787 A ENSESTG00000014905 ENSESTT00000037364 Transcript intron_variant - - - - - - rs2765416 10:27210686 A - - - intergenic_variant - - - - - - rs2993983 10:28796621 C - - - intergenic_variant - - - - - - rs552200 10:29464798 A - - - intergenic_variant - - - - - - rs2817839 10:29518645 C - ENSR00000642575 RegulatoryFeature regulatory_region_variant - - - - - - rs2817839 10:29518645 C - - - intergenic_variant - - - - - - rs1247799 10:29760992 G 6840 NM_003174.3 Transcript intron_variant - - - - - - rs1247799 10:29760992 G 6840 NM_021738.2 Transcript intron_variant - - - - - - rs1247799 10:29760992 G CCDS7163.1 CCDS7163.1 Transcript intron_variant - - - - - - rs1247799 10:29760992 G ENSESTG00000006692 ENSESTT00000017102 Transcript intron_variant - - - - - - rs1247799 10:29760992 G ENSESTG00000006635 ENSESTT00000016777 Transcript downstream_gene_variant - - - - - - DISTANCE=1563 rs1247799 10:29760992 G CCDS7164.1 CCDS7164.1 Transcript intron_variant - - - - - - rs1247799 10:29760992 G ENSESTG00000006692 ENSESTT00000017095 Transcript intron_variant - - - - - - rs1247799 10:29760992 G ENSESTG00000006692 ENSESTT00000017062 Transcript intron_variant - - - - - - rs1247799 10:29760992 G ENSESTG00000006635 ENSESTT00000016801 Transcript intron_variant - - - - - - rs1247799 10:29760992 G ENSESTG00000006635 ENSESTT00000016807 Transcript intron_variant - - - - - - rs1247799 10:29760992 G ENSESTG00000006692 ENSESTT00000017107 Transcript intron_variant - - - - - - rs1247799 10:29760992 G ENSESTG00000006635 ENSESTT00000016813 Transcript downstream_gene_variant - - - - - - DISTANCE=4474 rs2505923 10:29864062 C 6840 NM_003174.3 Transcript intron_variant - - - - - - rs2505923 10:29864062 C 6840 NM_021738.2 Transcript intron_variant - - - - - - rs2505923 10:29864062 C ENSESTG00000006661 ENSESTT00000016887 Transcript intron_variant - - - - - - rs2505923 10:29864062 C ENSESTG00000006661 ENSESTT00000016880 Transcript intron_variant - - - - - - rs2505923 10:29864062 C ENSESTG00000006661 ENSESTT00000016901 Transcript intron_variant - - - - - - rs1247418 10:29907036 G 6840 NM_003174.3 Transcript intron_variant - - - - - - rs1247418 10:29907036 G 6840 NM_021738.2 Transcript intron_variant - - - - - - rs1247418 10:29907036 G ENSESTG00000006661 ENSESTT00000016887 Transcript intron_variant - - - - - - rs1247418 10:29907036 G ENSESTG00000006661 ENSESTT00000016880 Transcript intron_variant - - - - - - rs1247418 10:29907036 G ENSESTG00000006661 ENSESTT00000016901 Transcript intron_variant - - - - - - rs1752796 10:29923083 G - ENSR00001422160 RegulatoryFeature regulatory_region_variant - - - - - - rs1752796 10:29923083 G 6840 NM_003174.3 Transcript intron_variant - - - - - - rs1752796 10:29923083 G 6840 NM_021738.2 Transcript intron_variant - - - - - - rs1752796 10:29923083 G ENSESTG00000006661 ENSESTT00000016887 Transcript intron_variant - - - - - - rs1752796 10:29923083 G ENSESTG00000006661 ENSESTT00000016880 Transcript intron_variant - - - - - - rs1752796 10:29923083 G ENSESTG00000006661 ENSESTT00000016901 Transcript intron_variant - - - - - - rs2479447 10:29978144 A - ENSR00000352624 RegulatoryFeature regulatory_region_variant - - - - - - rs2479447 10:29978144 A 6840 NM_003174.3 Transcript intron_variant - - - - - - rs2479447 10:29978144 A ENSESTG00000006661 ENSESTT00000016887 Transcript intron_variant - - - - - - rs2479447 10:29978144 A ENSESTG00000006661 ENSESTT00000016880 Transcript intron_variant - - - - - - rs2479447 10:29978144 A ENSESTG00000030460 ENSESTT00000076700 Transcript upstream_gene_variant - - - - - - DISTANCE=2593 rs2479447 10:29978144 A ENSESTG00000030460 ENSESTT00000076691 Transcript intron_variant - - - - - - rs4539210 10:30094157 G - ENSR00000352649 RegulatoryFeature regulatory_region_variant - - - - - - rs4539210 10:30094157 G - - - intergenic_variant - - - - - - rs2989437 10:30207910 C - - - intergenic_variant - - - - - - rs3122343 10:30927666 A - - - intergenic_variant - - - - - - rs3104004 10:30935491 G - - - intergenic_variant - - - - - - rs3104012 10:30940782 C - ENSR00000352794 RegulatoryFeature regulatory_region_variant - - - - - - rs3104012 10:30940782 C ENSESTG00000011874 ENSESTT00000029736 Transcript upstream_gene_variant - - - - - - DISTANCE=3685 rs10740829 10:30989188 C ENSESTG00000011880 ENSESTT00000029747 Transcript downstream_gene_variant - - - - - - DISTANCE=1796 rs10763836 10:31095090 C - - - intergenic_variant - - - - - - rs184421 10:31745366 G 6935 NM_030751.5 Transcript intron_variant - - - - - - rs184421 10:31745366 G 6935 NM_001128128.2 Transcript intron_variant - - - - - - rs184421 10:31745366 G CCDS7169.1 CCDS7169.1 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029828 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029795 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029843 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029826 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029834 Transcript intron_variant - - - - - - rs184421 10:31745366 G CCDS53506.1 CCDS53506.1 Transcript intron_variant - - - - - - rs184421 10:31745366 G CCDS53505.1 CCDS53505.1 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029842 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029832 Transcript intron_variant - - - - - - rs184421 10:31745366 G CCDS53507.1 CCDS53507.1 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029831 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029825 Transcript intron_variant - - - - - - rs184421 10:31745366 G 6935 NM_001174096.1 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029824 Transcript intron_variant - - - - - - rs184421 10:31745366 G CCDS44370.1 CCDS44370.1 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029838 Transcript intron_variant - - - - - - rs184421 10:31745366 G 6935 NM_001174095.1 Transcript intron_variant - - - - - - rs184421 10:31745366 G ENSESTG00000011891 ENSESTT00000029837 Transcript intron_variant - - - - - - rs184421 10:31745366 G 6935 NM_001174093.1 Transcript intron_variant - - - - - - rs184421 10:31745366 G 6935 NM_001174094.1 Transcript intron_variant - - - - - - rs2491269 10:32075438 T - - - intergenic_variant - - - - - - rs2998039 10:32461792 T - - - intergenic_variant - - - - - - rs4934988 10:33924202 G - - - intergenic_variant - - - - - - rs2445481 10:33969594 G ENSESTG00000002078 ENSESTT00000005120 Transcript upstream_gene_variant - - - - - - DISTANCE=4087 rs7084908 10:34170639 C - - - intergenic_variant - - - - - - rs170446 10:34313129 A - - - intergenic_variant - - - - - - rs2490657 10:35301647 A CCDS55709.1 CCDS55709.1 Transcript intron_variant - - - - - - rs2490657 10:35301647 A 8453 NM_003591.3 Transcript intron_variant - - - - - - rs2490657 10:35301647 A 8453 NM_001198778.1 Transcript intron_variant - - - - - - rs2490657 10:35301647 A CCDS7179.1 CCDS7179.1 Transcript intron_variant - - - - - - rs2490657 10:35301647 A 8453 NM_001198777.1 Transcript intron_variant - - - - - - rs2490657 10:35301647 A 8453 NM_001198779.1 Transcript intron_variant - - - - - - rs595981 10:36128798 T ENSESTG00000024947 ENSESTT00000062968 Transcript intron_variant - - - - - - rs635126 10:36162077 T ENSESTG00000024947 ENSESTT00000062968 Transcript intron_variant - - - - - - rs315648 10:36453021 T - - - intergenic_variant - - - - - - rs1332766 10:36848404 C - - - intergenic_variant - - - - - - rs2779305 10:37003943 C - - - intergenic_variant - - - - - - rs2804973 10:37059962 A - - - intergenic_variant - - - - - - rs2804975 10:37062992 G ENSESTG00000010249 ENSESTT00000025613 Transcript downstream_gene_variant - - - - - - DISTANCE=4261 rs1573155 10:37082972 T - - - intergenic_variant - - - - - - rs2798092 10:37092582 G - - - intergenic_variant - - - - - - rs1204488 10:37167853 A - - - intergenic_variant - - - - - - rs1192676 10:37175172 C - - - intergenic_variant - - - - - - rs941245 10:37211778 C - - - intergenic_variant - - - - - - rs2505156 10:37257139 A - - - intergenic_variant - - - - - - rs1815195 10:37270060 C - - - intergenic_variant - - - - - - rs2459436 10:37290245 A - - - intergenic_variant - - - - - - rs1200913 10:37369945 C - - - intergenic_variant - - - - - - rs1200879 10:37451334 G ENSESTG00000010223 ENSESTT00000025561 Transcript intron_variant - - - - - - rs1200879 10:37451334 G CCDS7193.1 CCDS7193.1 Transcript intron_variant - - - - - - rs1200879 10:37451334 G 91074 NM_052997.2 Transcript intron_variant - - - - - - rs1987242 10:37977819 C - - - intergenic_variant - - - - - - rs10764145 10:37990928 C - - - intergenic_variant - - - - - - rs200923 10:38124230 C ENSESTG00000019922 ENSESTT00000050028 Transcript intron_variant - - - - - - rs200923 10:38124230 C 57209 NM_021045.2 Transcript intron_variant - - - - - - rs200923 10:38124230 C CCDS58077.1 CCDS58077.1 Transcript intron_variant - - - - - - rs200923 10:38124230 C ENSESTG00000019922 ENSESTT00000049986 Transcript intron_variant - - - - - - rs200923 10:38124230 C ENSESTG00000019922 ENSESTT00000049948 Transcript intron_variant - - - - - - rs200923 10:38124230 C 57209 NM_001267605.1 Transcript intron_variant - - - - - - rs200923 10:38124230 C 57209 NM_001267606.1 Transcript intron_variant - - - - - - rs200923 10:38124230 C ENSESTG00000019922 ENSESTT00000049965 Transcript intron_variant - - - - - - rs200923 10:38124230 C ENSESTG00000019922 ENSESTT00000050018 Transcript intron_variant - - - - - - rs200923 10:38124230 C CCDS7194.1 CCDS7194.1 Transcript intron_variant - - - - - - rs200923 10:38124230 C ENSESTG00000019922 ENSESTT00000049998 Transcript intron_variant - - - - - - rs200923 10:38124230 C 57209 NM_001267607.1 Transcript intron_variant - - - - - - rs200923 10:38124230 C 57209 NM_001267597.1 Transcript intron_variant - - - - - - rs200923 10:38124230 C ENSESTG00000019922 ENSESTT00000050008 Transcript intron_variant - - - - - - rs2799500 10:38165018 C - - - intergenic_variant - - - - - - rs2749596 10:38247054 T 219749 NM_145011.2 Transcript intron_variant - - - - - - rs2749596 10:38247054 T CCDS7195.1 CCDS7195.1 Transcript intron_variant - - - - - - rs2749596 10:38247054 T ENSESTG00000019882 ENSESTT00000049907 Transcript intron_variant - - - - - - rs2749596 10:38247054 T ENSESTG00000019882 ENSESTT00000049887 Transcript intron_variant - - - - - - rs176847 10:38378777 G ENSESTG00000019666 ENSESTT00000049440 Transcript upstream_gene_variant - - - - - - DISTANCE=4502 rs176847 10:38378777 G ENSESTG00000019666 ENSESTT00000049428 Transcript upstream_gene_variant - - - - - - DISTANCE=4502 rs176847 10:38378777 G 7587 NM_001007094.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4487 rs176847 10:38378777 G 7587 NM_003421.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4487 rs176847 10:38378777 G ENSESTG00000019666 ENSESTT00000049455 Transcript upstream_gene_variant - - - - - - DISTANCE=4502 rs176847 10:38378777 G ENSESTG00000019666 ENSESTT00000049334 Transcript upstream_gene_variant - - - - - - DISTANCE=4489 rs176847 10:38378777 G ENSESTG00000019666 ENSESTT00000049364 Transcript upstream_gene_variant - - - - - - DISTANCE=4500 rs176847 10:38378777 G 7587 NM_001178101.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4487 rs176847 10:38378777 G ENSESTG00000019666 ENSESTT00000049358 Transcript upstream_gene_variant - - - - - - DISTANCE=4499 rs9703928 10:38751950 T ENSESTG00000019862 ENSESTT00000049781 Transcript intron_variant - - - - - - rs210234 10:43012009 C ENSESTG00000015032 ENSESTT00000037664 Transcript downstream_gene_variant - - - - - - DISTANCE=4266 rs210234 10:43012009 C 100129482 NR_026777.1 Transcript non_coding_exon_variant,nc_transcript_variant 5624 - - - - - rs210265 10:43044327 T ENSESTG00000015032 ENSESTT00000037664 Transcript intron_variant - - - - - - rs210265 10:43044327 T 100129482 NR_026777.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs210223 10:43057397 C - - - intergenic_variant - - - - - - rs3123598 10:43171332 A - - - intergenic_variant - - - - - - rs3121286 10:43277861 T - ENSR00000219810 RegulatoryFeature regulatory_region_variant - - - - - - rs3121286 10:43277861 T ENSESTG00000014570 ENSESTT00000036654 Transcript upstream_gene_variant - - - - - - DISTANCE=124 rs3121286 10:43277861 T ENSESTG00000014570 ENSESTT00000036669 Transcript upstream_gene_variant - - - - - - DISTANCE=391 rs3121286 10:43277861 T 9790 NM_014753.3 Transcript upstream_gene_variant - - - - - - DISTANCE=93 rs3121286 10:43277861 T CCDS7199.1 CCDS7199.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1982 rs3121286 10:43277861 T ENSESTG00000014570 ENSESTT00000036660 Transcript upstream_gene_variant - - - - - - DISTANCE=124 rs7917011 10:43652250 G CCDS7201.1 CCDS7201.1 Transcript intron_variant - - - - - - rs7917011 10:43652250 G 55454 NM_018590.3 Transcript intron_variant - - - - - - rs7917011 10:43652250 G ENSESTG00000014927 ENSESTT00000037395 Transcript intron_variant - - - - - - rs7917011 10:43652250 G ENSESTG00000014927 ENSESTT00000037403 Transcript intron_variant - - - - - - rs7917011 10:43652250 G ENSESTG00000014927 ENSESTT00000037414 Transcript upstream_gene_variant - - - - - - DISTANCE=3388 rs7917011 10:43652250 G ENSESTG00000014927 ENSESTT00000037409 Transcript intron_variant - - - - - - rs2505551 10:43706240 G ENSESTG00000014965 ENSESTT00000037504 Transcript intron_variant - - - - - - rs2505551 10:43706240 G ENSESTG00000014965 ENSESTT00000037521 Transcript intron_variant - - - - - - rs2505551 10:43706240 G ENSESTG00000014965 ENSESTT00000037516 Transcript intron_variant - - - - - - rs2505551 10:43706240 G 221002 NM_145313.2 Transcript intron_variant - - - - - - rs2505551 10:43706240 G CCDS7202.2 CCDS7202.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4676 rs3128239 10:44103923 C ENSESTG00000027011 ENSESTT00000068141 Transcript downstream_gene_variant - - - - - - DISTANCE=1075 rs3128239 10:44103923 C CCDS7205.2 CCDS7205.2 Transcript intron_variant - - - - - - rs3128239 10:44103923 C 220992 NM_145312.3 Transcript intron_variant - - - - - - rs3128239 10:44103923 C ENSESTG00000027011 ENSESTT00000068131 Transcript intron_variant - - - - - - rs3128241 10:44107220 C ENSESTG00000027011 ENSESTT00000068141 Transcript downstream_gene_variant - - - - - - DISTANCE=4372 rs3128241 10:44107220 C CCDS7205.2 CCDS7205.2 Transcript intron_variant - - - - - - rs3128241 10:44107220 C 220992 NM_145312.3 Transcript intron_variant - - - - - - rs3128241 10:44107220 C ENSESTG00000027011 ENSESTT00000068131 Transcript intron_variant - - - - - - rs3123682 10:44107283 T ENSESTG00000027011 ENSESTT00000068141 Transcript downstream_gene_variant - - - - - - DISTANCE=4435 rs3123682 10:44107283 T CCDS7205.2 CCDS7205.2 Transcript intron_variant - - - - - - rs3123682 10:44107283 T 220992 NM_145312.3 Transcript intron_variant - - - - - - rs3123682 10:44107283 T ENSESTG00000027011 ENSESTT00000068131 Transcript intron_variant - - - - - - rs2804041 10:44661611 C - - - intergenic_variant - - - - - - rs612784 10:44772448 C - - - intergenic_variant - - - - - - rs945564 10:44923176 G - - - intergenic_variant - - - - - - rs9421734 10:48448303 C - - - intergenic_variant - - - - - - rs7914062 10:49399553 T 143162 NM_001018071.3 Transcript intron_variant - - - - - - rs7914062 10:49399553 T ENSESTG00000029760 ENSESTT00000074860 Transcript intron_variant - - - - - - rs7914062 10:49399553 T ENSESTG00000029760 ENSESTT00000074874 Transcript intron_variant - - - - - - rs7914062 10:49399553 T CCDS31195.1 CCDS31195.1 Transcript intron_variant - - - - - - rs7919512 10:49817494 T 58504 NM_001256024.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4318 rs7919512 10:49817494 T 58504 NM_001256025.2 Transcript intron_variant - - - - - - rs7919512 10:49817494 T CCDS58081.1 CCDS58081.1 Transcript intron_variant - - - - - - rs7919512 10:49817494 T 58504 NR_045675.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7919512 10:49817494 T ENSESTG00000029607 ENSESTT00000074576 Transcript upstream_gene_variant - - - - - - DISTANCE=4321 rs7919512 10:49817494 T 58504 NM_021226.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4318 rs7919512 10:49817494 T ENSESTG00000029527 ENSESTT00000074282 Transcript downstream_gene_variant - - - - - - DISTANCE=4350 rs7919512 10:49817494 T CCDS58080.1 CCDS58080.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4653 rs7919512 10:49817494 T ENSESTG00000029607 ENSESTT00000074601 Transcript upstream_gene_variant - - - - - - DISTANCE=4321 rs7919512 10:49817494 T CCDS7227.1 CCDS7227.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4653 rs7919512 10:49817494 T ENSESTG00000029607 ENSESTT00000074549 Transcript intron_variant - - - - - - rs2940736 10:49969468 G 57705 NM_020945.1 Transcript intron_variant - - - - - - rs2940736 10:49969468 G CCDS44385.1 CCDS44385.1 Transcript intron_variant - - - - - - rs2671691 10:50096592 A ENSESTG00000005684 ENSESTT00000014412 Transcript intron_variant - - - - - - rs2671691 10:50096592 A ENSESTG00000005571 ENSESTT00000014196 Transcript intron_variant - - - - - - rs2671691 10:50096592 A ENSESTG00000005571 ENSESTT00000014186 Transcript intron_variant - - - - - - rs2671691 10:50096592 A 57705 NM_020945.1 Transcript intron_variant - - - - - - rs2671691 10:50096592 A CCDS44385.1 CCDS44385.1 Transcript intron_variant - - - - - - rs2671691 10:50096592 A ENSESTG00000005684 ENSESTT00000014414 Transcript intron_variant - - - - - - rs1258174 10:50956693 C 55753 NM_001143996.1 Transcript intron_variant - - - - - - rs1258174 10:50956693 C 55753 NM_018245.2 Transcript intron_variant - - - - - - rs1258174 10:50956693 C ENSESTG00000035524 ENSESTT00000089731 Transcript downstream_gene_variant - - - - - - DISTANCE=2191 rs1258174 10:50956693 C CCDS7234.1 CCDS7234.1 Transcript intron_variant - - - - - - rs1258174 10:50956693 C ENSESTG00000035524 ENSESTT00000089735 Transcript downstream_gene_variant - - - - - - DISTANCE=2301 rs1258174 10:50956693 C CCDS44390.1 CCDS44390.1 Transcript intron_variant - - - - - - rs1258174 10:50956693 C 55753 NM_001143997.1 Transcript intron_variant - - - - - - rs1258174 10:50956693 C CCDS44391.1 CCDS44391.1 Transcript intron_variant - - - - - - rs2579039 10:51041655 G 8505 NM_003631.2 Transcript intron_variant - - - - - - rs2579039 10:51041655 G ENSESTG00000035520 ENSESTT00000089724 Transcript intron_variant - - - - - - rs2092997 10:52252106 A ENSESTG00000010293 ENSESTT00000025766 Transcript intron_variant - - - - - - rs2092997 10:52252106 A ENSESTG00000010293 ENSESTT00000025760 Transcript intron_variant - - - - - - rs2092997 10:52252106 A ENSESTG00000010293 ENSESTT00000025751 Transcript intron_variant - - - - - - rs2092997 10:52252106 A ENSESTG00000010293 ENSESTT00000025748 Transcript intron_variant - - - - - - rs2092997 10:52252106 A ENSESTG00000010293 ENSESTT00000025745 Transcript intron_variant - - - - - - rs2092997 10:52252106 A 259230 NM_147156.3 Transcript intron_variant - - - - - - rs4469834 10:52571047 T CCDS7243.1 CCDS7243.1 Transcript intron_variant - - - - - - rs4469834 10:52571047 T 29974 NM_138933.2 Transcript intron_variant - - - - - - rs4469834 10:52571047 T ENSESTG00000010248 ENSESTT00000025637 Transcript intron_variant - - - - - - rs4469834 10:52571047 T CCDS7241.1 CCDS7241.1 Transcript intron_variant - - - - - - rs4469834 10:52571047 T 29974 NM_014576.3 Transcript intron_variant - - - - - - rs4469834 10:52571047 T CCDS7242.1 CCDS7242.1 Transcript intron_variant - - - - - - rs4469834 10:52571047 T 29974 NM_001198818.1 Transcript intron_variant - - - - - - rs4469834 10:52571047 T 29974 NM_001198820.1 Transcript intron_variant - - - - - - rs4469834 10:52571047 T 29974 NM_001198819.1 Transcript intron_variant - - - - - - rs4469834 10:52571047 T 29974 NM_138932.2 Transcript intron_variant - - - - - - rs1189271 10:52994813 T 5592 NM_006258.3 Transcript intron_variant - - - - - - rs1189271 10:52994813 T CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs1189271 10:52994813 T CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs1189271 10:52994813 T 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs1903958 10:53721015 C 5592 NM_006258.3 Transcript intron_variant - - - - - - rs1903958 10:53721015 C CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs1903958 10:53721015 C CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs1903958 10:53721015 C 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs10740410 10:53783969 C 5592 NM_006258.3 Transcript intron_variant - - - - - - rs10740410 10:53783969 C CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs10740410 10:53783969 C CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs10740410 10:53783969 C 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs4501941 10:53814622 C 5592 NM_006258.3 Transcript intron_variant - - - - - - rs4501941 10:53814622 C CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs4501941 10:53814622 C CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs4501941 10:53814622 C 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs6480705 10:53820267 A 5592 NM_006258.3 Transcript intron_variant - - - - - - rs6480705 10:53820267 A CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs6480705 10:53820267 A CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs6480705 10:53820267 A 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs6480706 10:53828367 G 5592 NM_006258.3 Transcript intron_variant - - - - - - rs6480706 10:53828367 G CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs6480706 10:53828367 G CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs6480706 10:53828367 G 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs4935312 10:53897578 C 5592 NM_006258.3 Transcript intron_variant - - - - - - rs4935312 10:53897578 C CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs4935312 10:53897578 C CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs4935312 10:53897578 C 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs1903990 10:53898891 C 5592 NM_006258.3 Transcript intron_variant - - - - - - rs1903990 10:53898891 C CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs1903990 10:53898891 C CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs1903990 10:53898891 C 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs1910535 10:53910927 T 5592 NM_006258.3 Transcript intron_variant - - - - - - rs1910535 10:53910927 T CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs1910535 10:53910927 T CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs1910535 10:53910927 T 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs7080049 10:53927777 G 5592 NM_006258.3 Transcript intron_variant - - - - - - rs7080049 10:53927777 G CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs7080049 10:53927777 G CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs7080049 10:53927777 G 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs1910547 10:53944566 G 5592 NM_006258.3 Transcript intron_variant - - - - - - rs1910547 10:53944566 G CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs1910547 10:53944566 G CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs1910547 10:53944566 G 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs2134759 10:53953915 C ENSESTG00000035232 ENSESTT00000089006 Transcript downstream_gene_variant - - - - - - DISTANCE=3214 rs2134759 10:53953915 C 5592 NM_006258.3 Transcript intron_variant - - - - - - rs2134759 10:53953915 C CCDS7244.1 CCDS7244.1 Transcript intron_variant - - - - - - rs2134759 10:53953915 C CCDS44399.1 CCDS44399.1 Transcript intron_variant - - - - - - rs2134759 10:53953915 C 5592 NM_001098512.2 Transcript intron_variant - - - - - - rs6480907 10:54359890 C ENSESTG00000035226 ENSESTT00000088977 Transcript intron_variant - - - - - - rs1919753 10:54374061 A ENSESTG00000035226 ENSESTT00000088977 Transcript intron_variant - - - - - - rs4423130 10:54473712 A ENSESTG00000035226 ENSESTT00000088977 Transcript intron_variant - - - - - - rs930505 10:54536397 C 4153 NM_000242.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4937 rs7475864 10:54550335 A - - - intergenic_variant - - - - - - rs4935048 10:54564368 A - - - intergenic_variant - - - - - - rs1573149 10:54748479 T - - - intergenic_variant - - - - - - rs10762957 10:55040014 A - - - intergenic_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142763.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142769.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142772.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_033056.3 Transcript intron_variant - - - - - - rs7070995 10:55886578 G CCDS44403.1 CCDS44403.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G CCDS44401.1 CCDS44401.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G CCDS44404.1 CCDS44404.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142773.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142767.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142770.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142771.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142764.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142766.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142765.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G CCDS7248.1 CCDS7248.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G CCDS44402.1 CCDS44402.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G CCDS44400.1 CCDS44400.1 Transcript intron_variant - - - - - - rs7070995 10:55886578 G 65217 NM_001142768.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142763.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142769.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142772.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_033056.3 Transcript intron_variant - - - - - - rs2384456 10:56166763 G CCDS44403.1 CCDS44403.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G CCDS44401.1 CCDS44401.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G CCDS44404.1 CCDS44404.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142773.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142767.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142770.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142771.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G ENSESTG00000013303 ENSESTT00000033364 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142764.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142766.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142765.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G CCDS7248.1 CCDS7248.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G CCDS44402.1 CCDS44402.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G CCDS44400.1 CCDS44400.1 Transcript intron_variant - - - - - - rs2384456 10:56166763 G 65217 NM_001142768.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G - ENSR00000355227 RegulatoryFeature regulatory_region_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142763.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142769.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142772.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_033056.3 Transcript intron_variant - - - - - - rs7076856 10:56381573 G CCDS44403.1 CCDS44403.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G CCDS44401.1 CCDS44401.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G CCDS44404.1 CCDS44404.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142773.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142767.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142770.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142771.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G ENSESTG00000013303 ENSESTT00000033364 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142764.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142766.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142765.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G CCDS7248.1 CCDS7248.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G CCDS44402.1 CCDS44402.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G CCDS44400.1 CCDS44400.1 Transcript intron_variant - - - - - - rs7076856 10:56381573 G 65217 NM_001142768.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142770.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142763.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142771.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T ENSESTG00000013303 ENSESTT00000033364 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142769.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142764.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142772.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142765.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142766.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_033056.3 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142773.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142767.1 Transcript intron_variant - - - - - - rs2152568 10:56483608 T 65217 NM_001142768.1 Transcript intron_variant - - - - - - rs7908874 10:56648494 A - - - intergenic_variant - - - - - - rs2222873 10:56779665 C - - - intergenic_variant - - - - - - rs4935574 10:56883811 T - - - intergenic_variant - - - - - - rs4144114 10:56892519 G - - - intergenic_variant - - - - - - rs2250203 10:56929444 T - - - intergenic_variant - - - - - - rs2463942 10:57374612 G ENSESTG00000035292 ENSESTT00000089120 Transcript intron_variant - - - - - - rs1916526 10:57376351 A ENSESTG00000035292 ENSESTT00000089120 Transcript intron_variant - - - - - - rs1916476 10:57479838 G - - - intergenic_variant - - - - - - rs7096457 10:57562564 T - - - intergenic_variant - - - - - - rs7477793 10:57847679 A - - - intergenic_variant - - - - - - rs6481244 10:58720985 A - - - intergenic_variant - - - - - - rs4542323 10:59366835 A - - - intergenic_variant - - - - - - rs2454053 10:59752046 T - ENSR00000355337 RegulatoryFeature regulatory_region_variant - - - - - - rs2454053 10:59752046 T - - - intergenic_variant - - - - - - rs1930477 10:59771332 C - - - intergenic_variant - - - - - - rs10740726 10:60087625 T - - - intergenic_variant - - - - - - rs1658482 10:60288981 T CCDS31206.1 CCDS31206.1 Transcript intron_variant - - - - - - rs1658482 10:60288981 T ENSESTG00000005092 ENSESTT00000012934 Transcript intron_variant - - - - - - rs1658482 10:60288981 T 80114 NM_001080512.1 Transcript intron_variant - - - - - - rs6481416 10:60401262 G - ENSR00001423677 RegulatoryFeature regulatory_region_variant - - - - - - rs6481416 10:60401262 G CCDS31206.1 CCDS31206.1 Transcript intron_variant - - - - - - rs6481416 10:60401262 G ENSESTG00000005092 ENSESTT00000012934 Transcript intron_variant - - - - - - rs6481416 10:60401262 G 80114 NM_001080512.1 Transcript intron_variant - - - - - - rs4948531 10:60407231 G - ENSR00001423680 RegulatoryFeature regulatory_region_variant - - - - - - rs4948531 10:60407231 G CCDS31206.1 CCDS31206.1 Transcript intron_variant - - - - - - rs4948531 10:60407231 G ENSESTG00000005092 ENSESTT00000012934 Transcript intron_variant - - - - - - rs4948531 10:60407231 G 80114 NM_001080512.1 Transcript intron_variant - - - - - - rs4141672 10:60421337 G - ENSR00000355422 RegulatoryFeature regulatory_region_variant - - - - - - rs4141672 10:60421337 G CCDS31206.1 CCDS31206.1 Transcript intron_variant - - - - - - rs4141672 10:60421337 G 80114 NM_001080512.1 Transcript intron_variant - - - - - - rs7902410 10:60424326 G CCDS31206.1 CCDS31206.1 Transcript intron_variant - - - - - - rs7902410 10:60424326 G 80114 NM_001080512.1 Transcript intron_variant - - - - - - rs1020084 10:60426747 G CCDS31206.1 CCDS31206.1 Transcript intron_variant - - - - - - rs1020084 10:60426747 G 80114 NM_001080512.1 Transcript intron_variant - - - - - - rs4948537 10:60433078 C CCDS31206.1 CCDS31206.1 Transcript intron_variant - - - - - - rs4948537 10:60433078 C 80114 NM_001080512.1 Transcript intron_variant - - - - - - rs10763582 10:60465184 C CCDS31206.1 CCDS31206.1 Transcript intron_variant - - - - - - rs10763582 10:60465184 C 80114 NM_001080512.1 Transcript intron_variant - - - - - - rs4948325 10:60836817 A - - - intergenic_variant - - - - - - rs4564283 10:60922445 C - - - intergenic_variant - - - - - - rs284594 10:61058640 A ENSESTG00000027310 ENSESTT00000068957 Transcript intron_variant - - - - - - rs284594 10:61058640 A CCDS31207.1 CCDS31207.1 Transcript intron_variant - - - - - - rs284594 10:61058640 A ENSESTG00000027310 ENSESTT00000068845 Transcript downstream_gene_variant - - - - - - DISTANCE=2273 rs284594 10:61058640 A CCDS7255.1 CCDS7255.1 Transcript intron_variant - - - - - - rs284594 10:61058640 A 220965 NM_001143773.1 Transcript intron_variant - - - - - - rs284594 10:61058640 A CCDS44406.1 CCDS44406.1 Transcript intron_variant - - - - - - rs284594 10:61058640 A CCDS53538.1 CCDS53538.1 Transcript intron_variant - - - - - - rs284594 10:61058640 A ENSESTG00000027310 ENSESTT00000068996 Transcript intron_variant - - - - - - rs284594 10:61058640 A 220965 NM_001166698.1 Transcript intron_variant - - - - - - rs284594 10:61058640 A 220965 NM_001001971.2 Transcript intron_variant - - - - - - rs284594 10:61058640 A ENSESTG00000027310 ENSESTT00000068922 Transcript intron_variant - - - - - - rs284594 10:61058640 A 220965 NM_198215.3 Transcript intron_variant - - - - - - rs2446714 10:61143194 C - ENSR00001423767 RegulatoryFeature regulatory_region_variant - - - - - - rs2446714 10:61143194 C - - - intergenic_variant - - - - - - rs185942 10:61192848 G - - - intergenic_variant - - - - - - rs7100866 10:61324791 C - - - intergenic_variant - - - - - - rs1875149 10:61341374 C - - - intergenic_variant - - - - - - rs1875146 10:61350108 G - - - intergenic_variant - - - - - - rs3862857 10:61372464 G - - - intergenic_variant - - - - - - rs10826328 10:61377227 T - - - intergenic_variant - - - - - - rs6481479 10:61429452 G ENSESTG00000027263 ENSESTT00000068735 Transcript intron_variant - - - - - - rs6481479 10:61429452 G ENSESTG00000027263 ENSESTT00000068726 Transcript intron_variant - - - - - - rs6481479 10:61429452 G 220963 NM_194298.2 Transcript intron_variant - - - - - - rs6481479 10:61429452 G ENSESTG00000027263 ENSESTT00000068710 Transcript intron_variant - - - - - - rs6481479 10:61429452 G ENSESTG00000027176 ENSESTT00000068485 Transcript intron_variant - - - - - - rs6481479 10:61429452 G ENSESTG00000027263 ENSESTT00000068718 Transcript intron_variant - - - - - - rs6481479 10:61429452 G ENSESTG00000027263 ENSESTT00000068745 Transcript intron_variant - - - - - - rs6481479 10:61429452 G ENSESTG00000027263 ENSESTT00000068750 Transcript intron_variant - - - - - - rs6481479 10:61429452 G ENSESTG00000027263 ENSESTT00000068692 Transcript intron_variant - - - - - - rs6481479 10:61429452 G CCDS7256.1 CCDS7256.1 Transcript intron_variant - - - - - - rs1171654 10:61446703 T ENSESTG00000027263 ENSESTT00000068735 Transcript intron_variant - - - - - - rs1171654 10:61446703 T ENSESTG00000027263 ENSESTT00000068726 Transcript intron_variant - - - - - - rs1171654 10:61446703 T 220963 NM_194298.2 Transcript intron_variant - - - - - - rs1171654 10:61446703 T ENSESTG00000027263 ENSESTT00000068710 Transcript intron_variant - - - - - - rs1171654 10:61446703 T ENSESTG00000027176 ENSESTT00000068485 Transcript intron_variant - - - - - - rs1171654 10:61446703 T ENSESTG00000027263 ENSESTT00000068718 Transcript intron_variant - - - - - - rs1171654 10:61446703 T ENSESTG00000027263 ENSESTT00000068745 Transcript intron_variant - - - - - - rs1171654 10:61446703 T ENSESTG00000027263 ENSESTT00000068750 Transcript intron_variant - - - - - - rs1171654 10:61446703 T ENSESTG00000027263 ENSESTT00000068692 Transcript intron_variant - - - - - - rs1171654 10:61446703 T CCDS7256.1 CCDS7256.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2654 rs7904845 10:62734873 T ENSESTG00000004441 ENSESTT00000011217 Transcript intron_variant - - - - - - rs7904845 10:62734873 T ENSESTG00000004441 ENSESTT00000011214 Transcript intron_variant - - - - - - rs7904845 10:62734873 T ENSESTG00000004441 ENSESTT00000011221 Transcript intron_variant - - - - - - rs7904845 10:62734873 T 9886 NR_024555.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7904845 10:62734873 T 9886 NR_024554.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs2998279 10:62938893 T - - - intergenic_variant - - - - - - rs7068014 10:63138957 G - - - intergenic_variant - - - - - - rs1456288 10:63350627 G - - - intergenic_variant - - - - - - rs2393789 10:63565422 G ENSESTG00000019596 ENSESTT00000049175 Transcript intron_variant - - - - - - rs7906602 10:63654103 G - - - intergenic_variant - - - - - - rs10740056 10:63733611 C ENSESTG00000019538 ENSESTT00000049098 Transcript intron_variant - - - - - - rs10740056 10:63733611 C ENSESTG00000019538 ENSESTT00000049091 Transcript intron_variant - - - - - - rs10740056 10:63733611 C CCDS31208.1 CCDS31208.1 Transcript intron_variant - - - - - - rs10740056 10:63733611 C 84159 NM_032199.2 Transcript intron_variant - - - - - - rs10740056 10:63733611 C ENSESTG00000019538 ENSESTT00000049113 Transcript intron_variant - - - - - - rs2893878 10:63770774 G ENSESTG00000019538 ENSESTT00000049098 Transcript intron_variant - - - - - - rs2893878 10:63770774 G ENSESTG00000019538 ENSESTT00000049091 Transcript intron_variant - - - - - - rs2893878 10:63770774 G CCDS31208.1 CCDS31208.1 Transcript intron_variant - - - - - - rs2893878 10:63770774 G 84159 NM_032199.2 Transcript intron_variant - - - - - - rs2893878 10:63770774 G ENSESTG00000019538 ENSESTT00000049113 Transcript intron_variant - - - - - - rs10821975 10:64064066 C - - - intergenic_variant - - - - - - rs9414769 10:64514696 G - - - intergenic_variant - - - - - - rs224081 10:64559718 C 84890 NM_032804.5 Transcript upstream_gene_variant - - - - - - DISTANCE=4798 rs224314 10:64617126 C - - - intergenic_variant - - - - - - rs2664327 10:64771220 C - - - intergenic_variant - - - - - - rs7089525 10:64930832 G ENSESTG00000022211 ENSESTT00000056250 Transcript intron_variant - - - - - - rs7089525 10:64930832 G CCDS41532.1 CCDS41532.1 Transcript intron_variant - - - - - - rs7089525 10:64930832 G 221037 NM_032776.1 Transcript intron_variant - - - - - - rs7089525 10:64930832 G ENSESTG00000022211 ENSESTT00000056309 Transcript intron_variant - - - - - - rs7089525 10:64930832 G 221037 NM_004241.2 Transcript intron_variant - - - - - - rs7089525 10:64930832 G CCDS44410.1 CCDS44410.1 Transcript intron_variant - - - - - - rs7089525 10:64930832 G ENSESTG00000022211 ENSESTT00000056285 Transcript intron_variant - - - - - - rs7089525 10:64930832 G ENSESTG00000022211 ENSESTT00000056322 Transcript intron_variant - - - - - - rs4511187 10:65018373 C ENSESTG00000022132 ENSESTT00000055872 Transcript intron_variant - - - - - - rs4511187 10:65018373 C ENSESTG00000022132 ENSESTT00000055880 Transcript intron_variant - - - - - - rs4511187 10:65018373 C CCDS41532.1 CCDS41532.1 Transcript intron_variant - - - - - - rs4511187 10:65018373 C ENSESTG00000022132 ENSESTT00000055835 Transcript intron_variant - - - - - - rs4511187 10:65018373 C 221037 NM_032776.1 Transcript intron_variant - - - - - - rs4511187 10:65018373 C ENSESTG00000022132 ENSESTT00000055918 Transcript intron_variant - - - - - - rs4511187 10:65018373 C 221037 NM_004241.2 Transcript intron_variant - - - - - - rs4511187 10:65018373 C ENSESTG00000022132 ENSESTT00000055943 Transcript intron_variant - - - - - - rs4511187 10:65018373 C ENSESTG00000022132 ENSESTT00000055789 Transcript intron_variant - - - - - - rs4746111 10:65103344 G 221037 NM_032776.1 Transcript intron_variant - - - - - - rs4746111 10:65103344 G CCDS41532.1 CCDS41532.1 Transcript intron_variant - - - - - - rs4746111 10:65103344 G ENSESTG00000022132 ENSESTT00000055789 Transcript intron_variant - - - - - - rs4746111 10:65103344 G ENSESTG00000022132 ENSESTT00000055835 Transcript intron_variant - - - - - - rs7100384 10:65286251 A ENSESTG00000022042 ENSESTT00000055653 Transcript intron_variant - - - - - - rs7100384 10:65286251 A 221035 NM_001001330.2 Transcript intron_variant - - - - - - rs7100384 10:65286251 A ENSESTG00000022042 ENSESTT00000055687 Transcript intron_variant - - - - - - rs7100384 10:65286251 A ENSESTG00000022042 ENSESTT00000055681 Transcript intron_variant - - - - - - rs7100384 10:65286251 A ENSESTG00000022132 ENSESTT00000055789 Transcript upstream_gene_variant - - - - - - DISTANCE=4641 rs7100384 10:65286251 A CCDS44411.1 CCDS44411.1 Transcript intron_variant - - - - - - rs10822192 10:65422825 T - - - intergenic_variant - - - - - - rs2256980 10:65799587 A ENSESTG00000029654 ENSESTT00000074582 Transcript upstream_gene_variant - - - - - - DISTANCE=2545 rs2578021 10:65845814 G ENSESTG00000029594 ENSESTT00000074443 Transcript downstream_gene_variant - - - - - - DISTANCE=3637 rs2578021 10:65845814 G ENSESTG00000029490 ENSESTT00000074220 Transcript intron_variant - - - - - - rs4745839 10:65894450 C ENSESTG00000029490 ENSESTT00000074220 Transcript intron_variant - - - - - - rs4522054 10:65975282 G - - - intergenic_variant - - - - - - rs7077685 10:65989544 C - - - intergenic_variant - - - - - - rs10761862 10:66482824 C - - - intergenic_variant - - - - - - rs1915642 10:66517104 G - - - intergenic_variant - - - - - - rs2962765 10:66632513 C - - - intergenic_variant - - - - - - rs2933441 10:66634352 A - - - intergenic_variant - - - - - - rs4746514 10:67139481 C - - - intergenic_variant - - - - - - rs1902392 10:67320344 G - - - intergenic_variant - - - - - - rs1902384 10:67361199 T - - - intergenic_variant - - - - - - rs1904703 10:67448513 T - - - intergenic_variant - - - - - - rs1869224 10:67593325 C ENSESTG00000013095 ENSESTT00000032824 Transcript downstream_gene_variant - - - - - - DISTANCE=3885 rs4746546 10:67852598 T ENSESTG00000009620 ENSESTT00000024119 Transcript intron_variant - - - - - - rs4746546 10:67852598 T 29119 NM_001127384.1 Transcript intron_variant - - - - - - rs4746546 10:67852598 T ENSESTG00000009648 ENSESTT00000024168 Transcript intron_variant - - - - - - rs4746546 10:67852598 T CCDS7269.1 CCDS7269.1 Transcript intron_variant - - - - - - rs4746546 10:67852598 T 29119 NM_013266.2 Transcript intron_variant - - - - - - rs6480146 10:67955260 G 29119 NM_001127384.1 Transcript intron_variant - - - - - - rs6480146 10:67955260 G CCDS7269.1 CCDS7269.1 Transcript intron_variant - - - - - - rs6480146 10:67955260 G 29119 NM_013266.2 Transcript intron_variant - - - - - - rs7911404 10:68797332 C CCDS7270.1 CCDS7270.1 Transcript intron_variant - - - - - - rs7911404 10:68797332 C 29119 NM_001127384.1 Transcript intron_variant - - - - - - rs7911404 10:68797332 C 347731 NM_178011.3 Transcript intron_variant - - - - - - rs7911404 10:68797332 C ENSESTG00000005177 ENSESTT00000013152 Transcript intron_variant - - - - - - rs7911404 10:68797332 C 29119 NM_013266.2 Transcript intron_variant - - - - - - rs7911404 10:68797332 C ENSESTG00000005177 ENSESTT00000013163 Transcript intron_variant - - - - - - rs7911404 10:68797332 C CCDS7269.1 CCDS7269.1 Transcript intron_variant - - - - - - rs7911404 10:68797332 C ENSESTG00000009635 ENSESTT00000024148 Transcript intron_variant - - - - - - rs2250623 10:68827814 T CCDS7270.1 CCDS7270.1 Transcript intron_variant - - - - - - rs2250623 10:68827814 T ENSESTG00000005177 ENSESTT00000013163 Transcript intron_variant - - - - - - rs2250623 10:68827814 T 29119 NM_001127384.1 Transcript intron_variant - - - - - - rs2250623 10:68827814 T ENSESTG00000009635 ENSESTT00000024148 Transcript intron_variant - - - - - - rs2250623 10:68827814 T 347731 NM_178011.3 Transcript intron_variant - - - - - - rs2250623 10:68827814 T CCDS7269.1 CCDS7269.1 Transcript intron_variant - - - - - - rs2250623 10:68827814 T 29119 NM_013266.2 Transcript intron_variant - - - - - - rs7097477 10:68975304 C 29119 NM_001127384.1 Transcript intron_variant - - - - - - rs7097477 10:68975304 C CCDS7269.1 CCDS7269.1 Transcript intron_variant - - - - - - rs7097477 10:68975304 C 29119 NM_013266.2 Transcript intron_variant - - - - - - rs4540739 10:69583419 A - ENSR00000356243 RegulatoryFeature regulatory_region_variant - - - - - - rs4540739 10:69583419 A ENSESTG00000005240 ENSESTT00000013316 Transcript intron_variant - - - - - - rs4540739 10:69583419 A CCDS7272.1 CCDS7272.1 Transcript intron_variant - - - - - - rs4540739 10:69583419 A ENSESTG00000005240 ENSESTT00000013330 Transcript intron_variant - - - - - - rs4540739 10:69583419 A CCDS7271.1 CCDS7271.1 Transcript intron_variant - - - - - - rs4540739 10:69583419 A 56521 NM_201262.1 Transcript intron_variant - - - - - - rs4540739 10:69583419 A 56521 NM_021800.2 Transcript intron_variant - - - - - - rs4746715 10:69638332 G - - - intergenic_variant - - - - - - rs660640 10:69760165 T CCDS41533.1 CCDS41533.1 Transcript intron_variant - - - - - - rs660640 10:69760165 T ENSESTG00000005208 ENSESTT00000013253 Transcript intron_variant - - - - - - rs660640 10:69760165 T ENSESTG00000005208 ENSESTT00000013251 Transcript intron_variant - - - - - - rs660640 10:69760165 T 26091 NM_015601.3 Transcript intron_variant - - - - - - rs660640 10:69760165 T 26091 NM_022079.2 Transcript intron_variant - - - - - - rs660640 10:69760165 T CCDS7274.1 CCDS7274.1 Transcript intron_variant - - - - - - rs4745955 10:70041343 T CCDS7277.2 CCDS7277.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2591 rs4745955 10:70041343 T CCDS44413.1 CCDS44413.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3673 rs4745955 10:70041343 T 64081 NM_001033083.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3495 rs4745955 10:70041343 T 64081 NM_022129.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1074 rs2063046 10:70978147 C CCDS7288.1 CCDS7288.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2045 rs2063046 10:70978147 C 80201 NM_025130.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1912 rs2063046 10:70978147 C ENSESTG00000014267 ENSESTT00000035716 Transcript upstream_gene_variant - - - - - - DISTANCE=1790 rs2063046 10:70978147 C ENSESTG00000014510 ENSESTT00000036332 Transcript downstream_gene_variant - - - - - - DISTANCE=4513 rs2394571 10:71215550 C ENSESTG00000014414 ENSESTT00000036131 Transcript intron_variant - - - - - - rs2394571 10:71215550 C CCDS7294.1 CCDS7294.1 Transcript intron_variant - - - - - - rs2394571 10:71215550 C ENSESTG00000014414 ENSESTT00000036127 Transcript intron_variant - - - - - - rs2394571 10:71215550 C ENSESTG00000014414 ENSESTT00000036135 Transcript upstream_gene_variant - - - - - - DISTANCE=3174 rs2394571 10:71215550 C 23555 NM_012339.3 Transcript intron_variant - - - - - - rs2812553 10:71366267 T - - - intergenic_variant - - - - - - rs2999169 10:71464910 T - - - intergenic_variant - - - - - - rs10762391 10:72319200 G - ENSR00001424518 RegulatoryFeature regulatory_region_variant - - - - - - rs10762391 10:72319200 G ENSESTG00000010356 ENSESTT00000025931 Transcript intron_variant - - - - - - rs10762391 10:72319200 G 27143 NM_014431.2 Transcript intron_variant - - - - - - rs10762391 10:72319200 G ENSESTG00000010356 ENSESTT00000025909 Transcript intron_variant - - - - - - rs10762391 10:72319200 G CCDS31215.1 CCDS31215.1 Transcript intron_variant - - - - - - rs2587478 10:72492212 C 140766 NM_139155.2 Transcript intron_variant - - - - - - rs2587478 10:72492212 C ENSESTG00000010382 ENSESTT00000025970 Transcript upstream_gene_variant - - - - - - DISTANCE=1502 rs2587478 10:72492212 C ENSESTG00000010379 ENSESTT00000025952 Transcript downstream_gene_variant - - - - - - DISTANCE=3110 rs2587478 10:72492212 C CCDS7306.1 CCDS7306.1 Transcript intron_variant - - - - - - rs2587478 10:72492212 C CCDS7307.1 CCDS7307.1 Transcript intron_variant - - - - - - rs2587478 10:72492212 C ENSESTG00000010382 ENSESTT00000025966 Transcript intron_variant - - - - - - rs2587478 10:72492212 C 140766 NM_080722.3 Transcript intron_variant - - - - - - rs1935150 10:72879786 C - - - intergenic_variant - - - - - - rs4747145 10:73035780 C 219699 NM_001244889.1 Transcript intron_variant - - - - - - rs4747145 10:73035780 C CCDS58083.1 CCDS58083.1 Transcript intron_variant - - - - - - rs4747145 10:73035780 C ENSESTG00000006087 ENSESTT00000015360 Transcript intron_variant - - - - - - rs4747145 10:73035780 C CCDS7309.1 CCDS7309.1 Transcript intron_variant - - - - - - rs4747145 10:73035780 C 219699 NM_170744.4 Transcript intron_variant - - - - - - rs7083996 10:73343413 G 64072 NM_022124.5 Transcript intron_variant - - - - - - rs7083996 10:73343413 G 64072 NM_052836.3 Transcript intron_variant - - - - - - rs7083996 10:73343413 G CCDS44429.1 CCDS44429.1 Transcript intron_variant - - - - - - rs7083996 10:73343413 G 64072 NM_001171931.1 Transcript intron_variant - - - - - - rs7083996 10:73343413 G ENSESTG00000006140 ENSESTT00000015486 Transcript intron_variant - - - - - - rs7083996 10:73343413 G 64072 NM_001171932.1 Transcript intron_variant - - - - - - rs7083996 10:73343413 G 64072 NM_001171930.1 Transcript intron_variant - - - - - - rs7083996 10:73343413 G ENSESTG00000006140 ENSESTT00000015490 Transcript intron_variant - - - - - - rs2394850 10:73759431 G - ENSR00001424686 RegulatoryFeature regulatory_region_variant - - - - - - rs2394850 10:73759431 G 9469 NM_004273.4 Transcript intron_variant - - - - - - rs10762519 10:74470520 G ENSESTG00000022125 ENSESTT00000055866 Transcript intron_variant - - - - - - rs10762519 10:74470520 G ENSESTG00000022125 ENSESTT00000055849 Transcript intron_variant - - - - - - rs10762519 10:74470520 G ENSESTG00000022125 ENSESTT00000055825 Transcript intron_variant - - - - - - rs10762519 10:74470520 G CCDS7317.1 CCDS7317.1 Transcript intron_variant - - - - - - rs10762519 10:74470520 G ENSESTG00000022125 ENSESTT00000055875 Transcript intron_variant - - - - - - rs10762519 10:74470520 G 90550 NM_138357.1 Transcript intron_variant - - - - - - rs2461917 10:74695287 C - ENSR00001424749 RegulatoryFeature regulatory_region_variant - - - - - - rs2461917 10:74695287 C ENSESTG00000022276 ENSESTT00000056202 Transcript intron_variant - - - - - - rs2461917 10:74695287 C CCDS7319.1 CCDS7319.1 Transcript downstream_gene_variant - - - - - - DISTANCE=88 rs2461917 10:74695287 C 84647 NM_032562.2 Transcript 3_prime_UTR_variant 743 - - - - - rs2461917 10:74695287 C CCDS7318.1 CCDS7318.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3005 rs2461917 10:74695287 C 170392 NM_152635.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2500 rs2461917 10:74695287 C ENSESTG00000022276 ENSESTT00000056215 Transcript downstream_gene_variant - - - - - - DISTANCE=2500 rs7910775 10:74912721 T 11319 NM_001135753.1 Transcript intron_variant - - - - - - rs7910775 10:74912721 T 11319 NM_001135752.1 Transcript intron_variant - - - - - - rs7910775 10:74912721 T ENSESTG00000004787 ENSESTT00000012216 Transcript intron_variant - - - - - - rs7910775 10:74912721 T ENSESTG00000004787 ENSESTT00000012150 Transcript intron_variant - - - - - - rs7910775 10:74912721 T CCDS44433.1 CCDS44433.1 Transcript intron_variant - - - - - - rs7910775 10:74912721 T CCDS7321.1 CCDS7321.1 Transcript intron_variant - - - - - - rs7910775 10:74912721 T 11319 NR_024203.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7910775 10:74912721 T 11319 NM_007265.2 Transcript intron_variant - - - - - - rs7910775 10:74912721 T ENSESTG00000004787 ENSESTT00000012165 Transcript intron_variant - - - - - - rs7910775 10:74912721 T ENSESTG00000004787 ENSESTT00000012214 Transcript intron_variant - - - - - - rs7910775 10:74912721 T ENSESTG00000004787 ENSESTT00000012224 Transcript intron_variant - - - - - - rs7910775 10:74912721 T CCDS44434.1 CCDS44434.1 Transcript intron_variant - - - - - - rs2395010 10:74942578 T - ENSR00000221109 RegulatoryFeature regulatory_region_variant - - - - - - rs2395010 10:74942578 T CCDS44435.1 CCDS44435.1 Transcript intron_variant - - - - - - rs2395010 10:74942578 T ENSESTG00000004354 ENSESTT00000011009 Transcript intron_variant - - - - - - rs2395010 10:74942578 T 317662 NM_173348.1 Transcript intron_variant - - - - - - rs2395010 10:74942578 T ENSESTG00000004354 ENSESTT00000011004 Transcript intron_variant - - - - - - rs2395010 10:74942578 T ENSESTG00000004354 ENSESTT00000011022 Transcript intron_variant - - - - - - rs2395010 10:74942578 T ENSESTG00000004354 ENSESTT00000011019 Transcript intron_variant - - - - - - rs10762549 10:75064689 G 118491 NM_145170.3 Transcript intron_variant - - - - - - rs10762549 10:75064689 G CCDS7324.3 CCDS7324.3 Transcript intron_variant - - - - - - rs1272655 10:75597523 A ENSESTG00000004595 ENSESTT00000011630 Transcript intron_variant - - - - - - rs1272655 10:75597523 A ENSESTG00000004595 ENSESTT00000011642 Transcript intron_variant - - - - - - rs1272655 10:75597523 A 818 NM_001204492.1 Transcript intron_variant - - - - - - rs1272655 10:75597523 A CCDS7337.1 CCDS7337.1 Transcript intron_variant - - - - - - rs1272655 10:75597523 A CCDS7338.1 CCDS7338.1 Transcript intron_variant - - - - - - rs1272655 10:75597523 A 818 NM_172171.2 Transcript intron_variant - - - - - - rs1272655 10:75597523 A ENSESTG00000004595 ENSESTT00000011640 Transcript intron_variant - - - - - - rs1272655 10:75597523 A ENSESTG00000004595 ENSESTT00000011628 Transcript intron_variant - - - - - - rs1272655 10:75597523 A 818 NM_172169.2 Transcript intron_variant - - - - - - rs1272655 10:75597523 A 818 NM_172173.2 Transcript intron_variant - - - - - - rs1272655 10:75597523 A 818 NM_001222.3 Transcript intron_variant - - - - - - rs1272655 10:75597523 A CCDS7336.1 CCDS7336.1 Transcript intron_variant - - - - - - rs1272655 10:75597523 A 818 NM_172170.4 Transcript intron_variant - - - - - - rs1272655 10:75597523 A ENSESTG00000004595 ENSESTT00000011644 Transcript intron_variant - - - - - - rs4745742 10:76023552 T CCDS55716.1 CCDS55716.1 Transcript intron_variant - - - - - - rs4745742 10:76023552 T ENSESTG00000012982 ENSESTT00000032609 Transcript intron_variant - - - - - - rs4745742 10:76023552 T CCDS55717.1 CCDS55717.1 Transcript intron_variant - - - - - - rs4745742 10:76023552 T 132 NM_001123.3 Transcript intron_variant - - - - - - rs4745742 10:76023552 T 132 NM_001202450.1 Transcript intron_variant - - - - - - rs4745742 10:76023552 T CCDS7343.1 CCDS7343.1 Transcript intron_variant - - - - - - rs4745742 10:76023552 T CCDS7344.1 CCDS7344.1 Transcript intron_variant - - - - - - rs4745742 10:76023552 T ENSESTG00000012982 ENSESTT00000032593 Transcript intron_variant - - - - - - rs4745742 10:76023552 T 132 NM_001202449.1 Transcript intron_variant - - - - - - rs4745742 10:76023552 T 132 NM_006721.3 Transcript intron_variant - - - - - - rs6480747 10:76412103 G CCDS55716.1 CCDS55716.1 Transcript intron_variant - - - - - - rs6480747 10:76412103 G ENSESTG00000012982 ENSESTT00000032609 Transcript intron_variant - - - - - - rs6480747 10:76412103 G CCDS55717.1 CCDS55717.1 Transcript intron_variant - - - - - - rs6480747 10:76412103 G 132 NM_001123.3 Transcript intron_variant - - - - - - rs6480747 10:76412103 G 132 NM_001202450.1 Transcript intron_variant - - - - - - rs6480747 10:76412103 G CCDS7343.1 CCDS7343.1 Transcript intron_variant - - - - - - rs6480747 10:76412103 G CCDS7344.1 CCDS7344.1 Transcript intron_variant - - - - - - rs6480747 10:76412103 G ENSESTG00000012982 ENSESTT00000032593 Transcript intron_variant - - - - - - rs6480747 10:76412103 G 132 NM_001202449.1 Transcript intron_variant - - - - - - rs6480747 10:76412103 G 132 NM_006721.3 Transcript intron_variant - - - - - - rs1407739 10:77602701 C - ENSR00000357438 RegulatoryFeature regulatory_region_variant - - - - - - rs1407739 10:77602701 C CCDS7351.1 CCDS7351.1 Transcript intron_variant - - - - - - rs1407739 10:77602701 C 83938 NM_032024.3 Transcript intron_variant - - - - - - rs2917195 10:78014916 A CCDS7351.1 CCDS7351.1 Transcript intron_variant - - - - - - rs2917195 10:78014916 A 83938 NM_032024.3 Transcript intron_variant - - - - - - rs2220610 10:78182628 C ENSESTG00000024541 ENSESTT00000062028 Transcript intron_variant - - - - - - rs2220610 10:78182628 C CCDS7351.1 CCDS7351.1 Transcript intron_variant - - - - - - rs2220610 10:78182628 C ENSESTG00000024541 ENSESTT00000062102 Transcript intron_variant - - - - - - rs2220610 10:78182628 C 83938 NM_032024.3 Transcript intron_variant - - - - - - rs4746392 10:78183229 T ENSESTG00000024541 ENSESTT00000062028 Transcript intron_variant - - - - - - rs4746392 10:78183229 T CCDS7351.1 CCDS7351.1 Transcript intron_variant - - - - - - rs4746392 10:78183229 T ENSESTG00000024541 ENSESTT00000062102 Transcript intron_variant - - - - - - rs4746392 10:78183229 T 83938 NM_032024.3 Transcript intron_variant - - - - - - rs1873460 10:78222781 A ENSESTG00000024541 ENSESTT00000062146 Transcript upstream_gene_variant - - - - - - DISTANCE=1791 rs1873460 10:78222781 A ENSESTG00000024541 ENSESTT00000062028 Transcript intron_variant - - - - - - rs1873460 10:78222781 A CCDS7351.1 CCDS7351.1 Transcript intron_variant - - - - - - rs1873460 10:78222781 A ENSESTG00000024541 ENSESTT00000062102 Transcript intron_variant - - - - - - rs1873460 10:78222781 A ENSESTG00000024541 ENSESTT00000062133 Transcript intron_variant - - - - - - rs1873460 10:78222781 A 83938 NM_032024.3 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079718 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079751 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079701 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079799 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079793 Transcript intron_variant - - - - - - rs2169672 10:78861925 A 3778 NM_001161352.1 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079841 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079828 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079782 Transcript intron_variant - - - - - - rs2169672 10:78861925 A 3778 NM_001161353.1 Transcript intron_variant - - - - - - rs2169672 10:78861925 A CCDS53545.1 CCDS53545.1 Transcript intron_variant - - - - - - rs2169672 10:78861925 A 3778 NM_001014797.2 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031281 ENSESTT00000078877 Transcript downstream_gene_variant - - - - - - DISTANCE=875 rs2169672 10:78861925 A CCDS7352.1 CCDS7352.1 Transcript intron_variant - - - - - - rs2169672 10:78861925 A 3778 NM_002247.3 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079788 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079872 Transcript intron_variant - - - - - - rs2169672 10:78861925 A ENSESTG00000031541 ENSESTT00000079733 Transcript intron_variant - - - - - - rs658906 10:79199078 T ENSESTG00000031541 ENSESTT00000079718 Transcript intron_variant - - - - - - rs658906 10:79199078 T ENSESTG00000031541 ENSESTT00000079751 Transcript intron_variant - - - - - - rs658906 10:79199078 T ENSESTG00000031541 ENSESTT00000079701 Transcript intron_variant - - - - - - rs658906 10:79199078 T 3778 NM_001161353.1 Transcript intron_variant - - - - - - rs658906 10:79199078 T CCDS53545.1 CCDS53545.1 Transcript intron_variant - - - - - - rs658906 10:79199078 T 3778 NM_001014797.2 Transcript intron_variant - - - - - - rs658906 10:79199078 T 3778 NM_002247.3 Transcript intron_variant - - - - - - rs658906 10:79199078 T CCDS7352.1 CCDS7352.1 Transcript intron_variant - - - - - - rs658906 10:79199078 T 3778 NM_001161352.1 Transcript intron_variant - - - - - - rs658906 10:79199078 T ENSESTG00000031541 ENSESTT00000079733 Transcript intron_variant - - - - - - rs2619633 10:79359505 G CCDS7352.1 CCDS7352.1 Transcript intron_variant - - - - - - rs2619633 10:79359505 G 3778 NM_002247.3 Transcript intron_variant - - - - - - rs2619633 10:79359505 G 3778 NM_001161352.1 Transcript intron_variant - - - - - - rs2619633 10:79359505 G ENSESTG00000031530 ENSESTT00000079514 Transcript intron_variant - - - - - - rs2619633 10:79359505 G 3778 NM_001161353.1 Transcript intron_variant - - - - - - rs2619633 10:79359505 G CCDS53545.1 CCDS53545.1 Transcript intron_variant - - - - - - rs2619633 10:79359505 G 3778 NM_001014797.2 Transcript intron_variant - - - - - - rs1649993 10:80069567 G ENSESTG00000011353 ENSESTT00000028510 Transcript intron_variant - - - - - - rs1649993 10:80069567 G ENSESTG00000011347 ENSESTT00000028496 Transcript intron_variant - - - - - - rs2395525 10:80084784 G ENSESTG00000011353 ENSESTT00000028510 Transcript intron_variant - - - - - - rs2395525 10:80084784 G ENSESTG00000011347 ENSESTT00000028496 Transcript intron_variant - - - - - - rs2117187 10:80252261 G ENSESTG00000011363 ENSESTT00000028520 Transcript intron_variant - - - - - - rs7083410 10:80291152 G - ENSR00001425197 RegulatoryFeature regulatory_region_variant - - - - - - rs7083410 10:80291152 G ENSESTG00000011363 ENSESTT00000028520 Transcript intron_variant - - - - - - rs2486696 10:80871245 G - ENSR00000357884 RegulatoryFeature regulatory_region_variant - - - - - - rs2486696 10:80871245 G ENSESTG00000009789 ENSESTT00000024494 Transcript intron_variant - - - - - - rs2486696 10:80871245 G 57178 NM_020338.3 Transcript intron_variant - - - - - - rs1250570 10:81044558 T ENSESTG00000009801 ENSESTT00000024550 Transcript intron_variant - - - - - - rs1250570 10:81044558 T ENSESTG00000009801 ENSESTT00000024571 Transcript intron_variant - - - - - - rs1250570 10:81044558 T ENSESTG00000009801 ENSESTT00000024559 Transcript intron_variant - - - - - - rs1250570 10:81044558 T 57178 NM_020338.3 Transcript intron_variant - - - - - - rs1250570 10:81044558 T CCDS7357.1 CCDS7357.1 Transcript intron_variant - - - - - - rs10733914 10:81223462 G - - - intergenic_variant - - - - - - rs9787639 10:81872581 C - - - intergenic_variant - - - - - - rs4934193 10:82216808 A - ENSR00000358126 RegulatoryFeature regulatory_region_variant - - - - - - rs4934193 10:82216808 A ENSESTG00000017599 ENSESTT00000044331 Transcript intron_variant - - - - - - rs4934193 10:82216808 A 81619 NM_030927.2 Transcript intron_variant - - - - - - rs4934193 10:82216808 A ENSESTG00000017599 ENSESTT00000044378 Transcript upstream_gene_variant - - - - - - DISTANCE=2333 rs4934193 10:82216808 A 81619 NM_001128309.1 Transcript intron_variant - - - - - - rs10748529 10:82289373 T ENSESTG00000017646 ENSESTT00000044462 Transcript downstream_gene_variant - - - - - - DISTANCE=3563 rs10748529 10:82289373 T ENSESTG00000017650 ENSESTT00000044490 Transcript 3_prime_UTR_variant 578 - - - - - rs2345212 10:82736939 T - - - intergenic_variant - - - - - - rs2207659 10:83605662 T - - - intergenic_variant - - - - - - rs2207663 10:83619034 T - - - intergenic_variant - - - - - - rs646028 10:85300211 G - - - intergenic_variant - - - - - - rs673577 10:85325292 G - - - intergenic_variant - - - - - - rs4393257 10:85403699 C - - - intergenic_variant - - - - - - rs1336202 10:86185654 G - ENSR00000358372 RegulatoryFeature regulatory_region_variant - - - - - - rs1336202 10:86185654 G ENSESTG00000027294 ENSESTT00000068882 Transcript splice_region_variant,intron_variant - - - - - - rs1336202 10:86185654 G ENSESTG00000027294 ENSESTT00000068923 Transcript splice_region_variant,intron_variant - - - - - - rs1336202 10:86185654 G CCDS31235.1 CCDS31235.1 Transcript splice_region_variant,intron_variant - - - - - - rs1336202 10:86185654 G 54462 NM_018999.2 Transcript splice_region_variant,intron_variant - - - - - - rs1336202 10:86185654 G ENSESTG00000027294 ENSESTT00000068895 Transcript splice_region_variant,intron_variant - - - - - - rs1336202 10:86185654 G ENSESTG00000027294 ENSESTT00000068860 Transcript splice_region_variant,intron_variant - - - - - - rs1336202 10:86185654 G ENSESTG00000027294 ENSESTT00000068913 Transcript splice_region_variant,intron_variant - - - - - - rs1336202 10:86185654 G ENSESTG00000027294 ENSESTT00000068900 Transcript splice_region_variant,intron_variant - - - - - - rs7904291 10:86973012 C - ENSR00000643469 RegulatoryFeature regulatory_region_variant - - - - - - rs7904291 10:86973012 C - - - intergenic_variant - - - - - - rs10749531 10:87764919 A 2894 NM_017551.2 Transcript intron_variant - - - - - - rs10749531 10:87764919 A CCDS31236.1 CCDS31236.1 Transcript intron_variant - - - - - - rs7089327 10:88106335 T - ENSR00000358474 RegulatoryFeature regulatory_region_variant - - - - - - rs7089327 10:88106335 T 2894 NM_017551.2 Transcript intron_variant - - - - - - rs7089327 10:88106335 T CCDS31236.1 CCDS31236.1 Transcript intron_variant - - - - - - rs7089327 10:88106335 T ENSESTG00000028451 ENSESTT00000071535 Transcript intron_variant - - - - - - rs2675684 10:88398818 T - - - intergenic_variant - - - - - - rs2736687 10:88425754 G ENSESTG00000028036 ENSESTT00000070761 Transcript upstream_gene_variant - - - - - - DISTANCE=2567 rs2736687 10:88425754 G CCDS44450.1 CCDS44450.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2695 rs2736687 10:88425754 G 11155 NM_001171611.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2672 rs2736687 10:88425754 G ENSESTG00000028036 ENSESTT00000070712 Transcript upstream_gene_variant - - - - - - DISTANCE=2510 rs2736687 10:88425754 G ENSESTG00000028036 ENSESTT00000070706 Transcript upstream_gene_variant - - - - - - DISTANCE=2510 rs2736687 10:88425754 G 11155 NM_001080116.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2567 rs2736687 10:88425754 G ENSESTG00000028036 ENSESTT00000070693 Transcript upstream_gene_variant - - - - - - DISTANCE=2510 rs2736687 10:88425754 G CCDS7376.1 CCDS7376.1 Transcript downstream_gene_variant - - - - - - DISTANCE=246 rs2736687 10:88425754 G CCDS53549.1 CCDS53549.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2695 rs2736687 10:88425754 G 11155 NM_001080114.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2672 rs2736687 10:88425754 G 11155 NM_001171610.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2452 rs2736687 10:88425754 G 94233 NM_001030015.2 Transcript 3_prime_UTR_variant 1943 - - - - - rs2736687 10:88425754 G CCDS41544.1 CCDS41544.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2695 rs2736687 10:88425754 G 94233 NM_033282.3 Transcript 3_prime_UTR_variant 1910 - - - - - rs2736687 10:88425754 G ENSESTG00000028013 ENSESTT00000070508 Transcript downstream_gene_variant - - - - - - DISTANCE=2215 rs2736687 10:88425754 G CCDS7377.1 CCDS7377.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2695 rs2736687 10:88425754 G CCDS31237.1 CCDS31237.1 Transcript downstream_gene_variant - - - - - - DISTANCE=246 rs2736687 10:88425754 G 11155 NM_001080115.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2672 rs2736687 10:88425754 G ENSESTG00000028013 ENSESTT00000070493 Transcript downstream_gene_variant - - - - - - DISTANCE=2301 rs2736687 10:88425754 G ENSESTG00000028036 ENSESTT00000070675 Transcript upstream_gene_variant - - - - - - DISTANCE=2510 rs2736687 10:88425754 G ENSESTG00000028036 ENSESTT00000070723 Transcript upstream_gene_variant - - - - - - DISTANCE=2510 rs2736687 10:88425754 G CCDS53550.1 CCDS53550.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2695 rs2736687 10:88425754 G ENSESTG00000028036 ENSESTT00000070546 Transcript upstream_gene_variant - - - - - - DISTANCE=795 rs2736687 10:88425754 G ENSESTG00000028036 ENSESTT00000070688 Transcript upstream_gene_variant - - - - - - DISTANCE=2510 rs2736687 10:88425754 G 11155 NM_007078.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2672 rs2736687 10:88425754 G CCDS41545.1 CCDS41545.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2695 rs7478354 10:88627505 A ENSESTG00000028184 ENSESTT00000071130 Transcript intron_variant - - - - - - rs7478354 10:88627505 A 657 NM_004329.2 Transcript intron_variant - - - - - - rs7478354 10:88627505 A ENSESTG00000028184 ENSESTT00000071039 Transcript intron_variant - - - - - - rs7478354 10:88627505 A ENSESTG00000028184 ENSESTT00000071053 Transcript intron_variant - - - - - - rs7478354 10:88627505 A ENSESTG00000028184 ENSESTT00000071106 Transcript intron_variant - - - - - - rs1923937 10:88839070 A CCDS7382.1 CCDS7382.1 Transcript intron_variant - - - - - - rs1923937 10:88839070 A ENSESTG00000032077 ENSESTT00000081081 Transcript intron_variant - - - - - - rs1923937 10:88839070 A ENSESTG00000032077 ENSESTT00000081089 Transcript intron_variant - - - - - - rs1923937 10:88839070 A ENSESTG00000032077 ENSESTT00000081048 Transcript intron_variant - - - - - - rs1923937 10:88839070 A ENSESTG00000032077 ENSESTT00000081062 Transcript intron_variant - - - - - - rs1923937 10:88839070 A ENSESTG00000032077 ENSESTT00000081071 Transcript intron_variant - - - - - - rs1923937 10:88839070 A 2746 NM_005271.3 Transcript intron_variant - - - - - - rs1923937 10:88839070 A ENSESTG00000032077 ENSESTT00000081076 Transcript intron_variant - - - - - - rs10218958 10:89436591 C CCDS7385.1 CCDS7385.1 Transcript intron_variant - - - - - - rs10218958 10:89436591 C CCDS44453.1 CCDS44453.1 Transcript intron_variant - - - - - - rs10218958 10:89436591 C 9060 NM_001015880.1 Transcript intron_variant - - - - - - rs10218958 10:89436591 C ENSESTG00000031870 ENSESTT00000080511 Transcript intron_variant - - - - - - rs10218958 10:89436591 C ENSESTG00000031870 ENSESTT00000080501 Transcript intron_variant - - - - - - rs10218958 10:89436591 C 9060 NM_004670.3 Transcript intron_variant - - - - - - rs10218958 10:89436591 C ENSESTG00000031870 ENSESTT00000080553 Transcript intron_variant - - - - - - rs2735361 10:89687071 T - ENSR00001425647 RegulatoryFeature regulatory_region_variant - - - - - - rs2735361 10:89687071 T CCDS31238.1 CCDS31238.1 Transcript intron_variant - - - - - - rs2735361 10:89687071 T 5728 NM_000314.4 Transcript intron_variant - - - - - - rs2735361 10:89687071 T ENSESTG00000031967 ENSESTT00000080717 Transcript intron_variant - - - - - - rs2735361 10:89687071 T ENSESTG00000031967 ENSESTT00000080707 Transcript intron_variant - - - - - - rs7101076 10:90374719 C - - - intergenic_variant - - - - - - rs1777950 10:91678103 A - - - intergenic_variant - - - - - - rs7086739 10:91902059 C - - - intergenic_variant - - - - - - rs2765795 10:91968308 G - - - intergenic_variant - - - - - - rs699193 10:92000309 A - - - intergenic_variant - - - - - - rs1274342 10:92269395 C - - - intergenic_variant - - - - - - rs4933619 10:92654247 C ENSESTG00000011296 ENSESTT00000028415 Transcript upstream_gene_variant - - - - - - DISTANCE=1275 rs4933619 10:92654247 C CCDS44458.1 CCDS44458.1 Transcript intron_variant - - - - - - rs4933619 10:92654247 C 10556 NM_001104546.1 Transcript intron_variant - - - - - - rs4933619 10:92654247 C 10556 NM_006413.4 Transcript intron_variant - - - - - - rs4933619 10:92654247 C CCDS7411.1 CCDS7411.1 Transcript intron_variant - - - - - - rs4933619 10:92654247 C ENSESTG00000011296 ENSESTT00000028394 Transcript intron_variant - - - - - - rs4933619 10:92654247 C ENSESTG00000011296 ENSESTT00000028402 Transcript intron_variant - - - - - - rs1835736 10:92873140 C - - - intergenic_variant - - - - - - rs2454530 10:93113825 G ENSESTG00000021569 ENSESTT00000054100 Transcript upstream_gene_variant - - - - - - DISTANCE=3186 rs2454530 10:93113825 G 100188947 NR_024467.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7910297 10:93231197 A 143279 NM_182765.3 Transcript intron_variant - - - - - - rs7910297 10:93231197 A CCDS7414.1 CCDS7414.1 Transcript intron_variant - - - - - - rs7910297 10:93231197 A ENSESTG00000021207 ENSESTT00000053314 Transcript intron_variant - - - - - - rs7910297 10:93231197 A 100188947 NR_024467.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7089991 10:93701472 A CCDS7419.1 CCDS7419.1 Transcript intron_variant - - - - - - rs7089991 10:93701472 A 9044 NM_003972.2 Transcript intron_variant - - - - - - rs7089991 10:93701472 A ENSESTG00000017600 ENSESTT00000044424 Transcript intron_variant - - - - - - rs7089991 10:93701472 A ENSESTG00000017600 ENSESTT00000044386 Transcript intron_variant - - - - - - rs2676811 10:93841227 G CCDS53553.1 CCDS53553.1 Transcript synonymous_variant 1677 1677 559 Y taT/taC - rs2676811 10:93841227 G 22849 NM_014912.4 Transcript synonymous_variant 1923 1719 573 Y taT/taC - rs2676811 10:93841227 G CCDS31246.1 CCDS31246.1 Transcript synonymous_variant 1719 1719 573 Y taT/taC - rs2676811 10:93841227 G ENSESTG00000018854 ENSESTT00000047486 Transcript synonymous_variant 870 795 265 Y taT/taC - rs2676811 10:93841227 G ENSESTG00000018854 ENSESTT00000047506 Transcript synonymous_variant 317 105 35 Y taT/taC - rs2676811 10:93841227 G 22849 NM_001178137.1 Transcript synonymous_variant 1799 1677 559 Y taT/taC - rs2488054 10:94432466 A - - - intergenic_variant - - - - - - rs10748587 10:94727628 A - ENSR00000221894 RegulatoryFeature regulatory_region_variant - - - - - - rs10748587 10:94727628 A CCDS31247.1 CCDS31247.1 Transcript intron_variant - - - - - - rs10748587 10:94727628 A ENSESTG00000019186 ENSESTT00000048441 Transcript intron_variant - - - - - - rs10748587 10:94727628 A ENSESTG00000019186 ENSESTT00000048472 Transcript intron_variant - - - - - - rs10748587 10:94727628 A CCDS7424.2 CCDS7424.2 Transcript intron_variant - - - - - - rs10748587 10:94727628 A 54536 NM_001013848.2 Transcript intron_variant - - - - - - rs10748587 10:94727628 A 54536 NM_019053.4 Transcript intron_variant - - - - - - rs4919490 10:95515015 C ENSESTG00000019506 ENSESTT00000049078 Transcript upstream_gene_variant - - - - - - DISTANCE=2589 rs4919490 10:95515015 C 9211 NM_005097.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2551 rs4919490 10:95515015 C CCDS7431.1 CCDS7431.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2887 rs4919490 10:95515015 C ENSESTG00000019506 ENSESTT00000049080 Transcript upstream_gene_variant - - - - - - DISTANCE=2589 rs4919490 10:95515015 C ENSESTG00000019506 ENSESTT00000049063 Transcript upstream_gene_variant - - - - - - DISTANCE=2589 rs2861146 10:97640219 A ENSESTG00000018356 ENSESTT00000046217 Transcript intron_variant - - - - - - rs2861146 10:97640219 A 953 NM_001164178.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3196 rs2861146 10:97640219 A 953 NM_001164181.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3196 rs2861146 10:97640219 A 953 NM_001098175.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3196 rs2861146 10:97640219 A 953 NM_001776.5 Transcript downstream_gene_variant - - - - - - DISTANCE=3196 rs2861146 10:97640219 A 953 NM_001164179.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3196 rs2861146 10:97640219 A ENSESTG00000018356 ENSESTT00000046206 Transcript intron_variant - - - - - - rs2861146 10:97640219 A 953 NM_001164182.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3196 rs2861146 10:97640219 A 728558 NR_038444.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2861146 10:97640219 A 953 NM_001164183.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3196 rs2607865 10:97872022 G - - - intergenic_variant - - - - - - rs1184616 10:98003800 A 29760 NR_047681.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1184616 10:98003800 A CCDS44464.1 CCDS44464.1 Transcript intron_variant - - - - - - rs1184616 10:98003800 A ENSESTG00000011246 ENSESTT00000028214 Transcript intron_variant - - - - - - rs1184616 10:98003800 A 29760 NM_013314.3 Transcript intron_variant - - - - - - rs1184616 10:98003800 A 29760 NR_047683.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1184616 10:98003800 A 29760 NM_001258440.1 Transcript intron_variant - - - - - - rs1184616 10:98003800 A 29760 NM_001258442.1 Transcript intron_variant - - - - - - rs1184616 10:98003800 A 29760 NM_001258441.1 Transcript intron_variant - - - - - - rs1184616 10:98003800 A ENSESTG00000011246 ENSESTT00000028223 Transcript intron_variant - - - - - - rs1184616 10:98003800 A ENSESTG00000011246 ENSESTT00000028219 Transcript intron_variant - - - - - - rs1184616 10:98003800 A CCDS58091.1 CCDS58091.1 Transcript intron_variant - - - - - - rs1184616 10:98003800 A 29760 NR_047682.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1184616 10:98003800 A 29760 NM_001114094.1 Transcript intron_variant - - - - - - rs1184616 10:98003800 A CCDS7446.1 CCDS7446.1 Transcript intron_variant - - - - - - rs1184616 10:98003800 A 29760 NR_047680.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2861826 10:98772422 G ENSESTG00000027883 ENSESTT00000070336 Transcript intron_variant - - - - - - rs2861826 10:98772422 G ENSESTG00000027883 ENSESTT00000070360 Transcript intron_variant - - - - - - rs2861826 10:98772422 G CCDS7453.1 CCDS7453.1 Transcript intron_variant - - - - - - rs2861826 10:98772422 G 6585 NM_003061.2 Transcript intron_variant - - - - - - rs2861826 10:98772422 G ENSESTG00000027883 ENSESTT00000070304 Transcript intron_variant - - - - - - rs3862024 10:99831403 A - - - intergenic_variant - - - - - - rs10748713 10:99894233 G - ENSR00000643703 RegulatoryFeature regulatory_region_variant - - - - - - rs10748713 10:99894233 G 27291 NM_138469.2 Transcript upstream_gene_variant - - - - - - DISTANCE=148 rs10748713 10:99894233 G 27291 NM_014472.4 Transcript upstream_gene_variant - - - - - - DISTANCE=148 rs10748713 10:99894233 G 27291 NM_001256620.1 Transcript upstream_gene_variant - - - - - - DISTANCE=148 rs10748713 10:99894233 G ENSESTG00000005377 ENSESTT00000013651 Transcript upstream_gene_variant - - - - - - DISTANCE=187 rs10748713 10:99894233 G 27291 NM_001256621.1 Transcript upstream_gene_variant - - - - - - DISTANCE=148 rs10748713 10:99894233 G 27291 NM_001256619.1 Transcript upstream_gene_variant - - - - - - DISTANCE=148 rs10748713 10:99894233 G ENSESTG00000005377 ENSESTT00000013647 Transcript upstream_gene_variant - - - - - - DISTANCE=180 rs2105430 10:100561287 T CCDS53568.1 CCDS53568.1 Transcript intron_variant - - - - - - rs2105430 10:100561287 T 60495 NM_001166244.1 Transcript intron_variant - - - - - - rs2105430 10:100561287 T 60495 NM_021828.4 Transcript intron_variant - - - - - - rs2105430 10:100561287 T CCDS7477.1 CCDS7477.1 Transcript intron_variant - - - - - - rs2105430 10:100561287 T CCDS53567.1 CCDS53567.1 Transcript intron_variant - - - - - - rs2105430 10:100561287 T CCDS53566.1 CCDS53566.1 Transcript intron_variant - - - - - - rs2105430 10:100561287 T 60495 NM_001166246.1 Transcript intron_variant - - - - - - rs2105430 10:100561287 T 60495 NM_001166245.1 Transcript intron_variant - - - - - - rs10786543 10:101164902 C CCDS7479.1 CCDS7479.1 Transcript intron_variant - - - - - - rs10786543 10:101164902 C ENSESTG00000027270 ENSESTT00000068798 Transcript downstream_gene_variant - - - - - - DISTANCE=1050 rs10786543 10:101164902 C 2805 NM_002079.2 Transcript intron_variant - - - - - - rs10786543 10:101164902 C ENSESTG00000027270 ENSESTT00000068787 Transcript downstream_gene_variant - - - - - - DISTANCE=1059 rs2804420 10:101640519 T - ENSR00000360341 RegulatoryFeature regulatory_region_variant - - - - - - rs2804420 10:101640519 T CCDS7485.1 CCDS7485.1 Transcript intron_variant - - - - - - rs2804420 10:101640519 T 23268 NM_015221.2 Transcript intron_variant - - - - - - rs2804953 10:101874506 C - - - intergenic_variant - - - - - - rs4399273 10:102277664 C ENSESTG00000009112 ENSESTT00000022899 Transcript intron_variant - - - - - - rs4399273 10:102277664 C ENSESTG00000009112 ENSESTT00000022879 Transcript intron_variant - - - - - - rs4399273 10:102277664 C 25956 NM_015490.3 Transcript intron_variant - - - - - - rs4399273 10:102277664 C ENSESTG00000009112 ENSESTT00000022905 Transcript intron_variant - - - - - - rs4399273 10:102277664 C CCDS7495.1 CCDS7495.1 Transcript upstream_gene_variant - - - - - - DISTANCE=955 rs1891913 10:102338761 A - - - intergenic_variant - - - - - - rs7909745 10:102494727 G ENSESTG00000009065 ENSESTT00000022754 Transcript upstream_gene_variant - - - - - - DISTANCE=633 rs2742051 10:102884387 G ENSESTG00000035650 ENSESTT00000090067 Transcript intron_variant - - - - - - rs2742051 10:102884387 G 100038246 NM_001085398.1 Transcript intron_variant - - - - - - rs2742051 10:102884387 G ENSESTG00000035650 ENSESTT00000090068 Transcript intron_variant - - - - - - rs1767633 10:102927748 A - - - intergenic_variant - - - - - - rs11191100 10:103474978 G - - - intergenic_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000090008 Transcript intron_variant - - - - - - rs7913120 10:103555471 T 10724 NM_001142434.1 Transcript intron_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000089998 Transcript intron_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000090013 Transcript intron_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000089997 Transcript downstream_gene_variant - - - - - - DISTANCE=3677 rs7913120 10:103555471 T CCDS44471.1 CCDS44471.1 Transcript intron_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000090009 Transcript intron_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000090002 Transcript intron_variant - - - - - - rs7913120 10:103555471 T CCDS7520.1 CCDS7520.1 Transcript intron_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000090000 Transcript intron_variant - - - - - - rs7913120 10:103555471 T 10724 NM_012215.3 Transcript intron_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000089996 Transcript intron_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000090004 Transcript downstream_gene_variant - - - - - - DISTANCE=3677 rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000090007 Transcript intron_variant - - - - - - rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000089999 Transcript downstream_gene_variant - - - - - - DISTANCE=3677 rs7913120 10:103555471 T ENSESTG00000035623 ENSESTT00000090001 Transcript downstream_gene_variant - - - - - - DISTANCE=3677 rs7077838 10:103661420 G - ENSR00000360671 RegulatoryFeature regulatory_region_variant - - - - - - rs7077838 10:103661420 G 79591 NM_024541.2 Transcript intron_variant - - - - - - rs7077838 10:103661420 G ENSESTG00000035622 ENSESTT00000089978 Transcript intron_variant - - - - - - rs7077838 10:103661420 G CCDS41563.1 CCDS41563.1 Transcript intron_variant - - - - - - rs7077838 10:103661420 G ENSESTG00000014817 ENSESTT00000037232 Transcript intron_variant - - - - - - rs7077838 10:103661420 G ENSESTG00000014817 ENSESTT00000037230 Transcript intron_variant - - - - - - rs7077838 10:103661420 G ENSESTG00000035621 ENSESTT00000089977 Transcript intron_variant - - - - - - rs4261220 10:103957489 G - - - intergenic_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078564 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078536 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078506 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078446 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078465 Transcript downstream_gene_variant - - - - - - DISTANCE=2459 rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078559 Transcript intron_variant - - - - - - rs3862029 10:104124887 G 8729 NM_004193.2 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078473 Transcript downstream_gene_variant - - - - - - DISTANCE=4733 rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078585 Transcript upstream_gene_variant - - - - - - DISTANCE=2585 rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078488 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078529 Transcript downstream_gene_variant - - - - - - DISTANCE=2459 rs3862029 10:104124887 G 8729 NM_001199378.1 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078518 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078391 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078422 Transcript intron_variant - - - - - - rs3862029 10:104124887 G CCDS7533.1 CCDS7533.1 Transcript intron_variant - - - - - - rs3862029 10:104124887 G 8729 NM_001199379.1 Transcript intron_variant - - - - - - rs3862029 10:104124887 G ENSESTG00000030945 ENSESTT00000078581 Transcript upstream_gene_variant - - - - - - DISTANCE=2585 rs7081280 10:104192488 G - ENSR00000117391 RegulatoryFeature regulatory_region_variant - - - - - - rs7081280 10:104192488 G ENSESTG00000013853 ENSESTT00000034683 Transcript intron_variant - - - - - - rs7081280 10:104192488 G 79004 NM_024040.2 Transcript upstream_gene_variant - - - - - - DISTANCE=65 rs7081280 10:104192488 G ENSESTG00000014599 ENSESTT00000036608 Transcript upstream_gene_variant - - - - - - DISTANCE=139 rs7081280 10:104192488 G 574447 NR_030169.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3781 rs7081280 10:104192488 G ENSESTG00000014599 ENSESTT00000036612 Transcript upstream_gene_variant - - - - - - DISTANCE=163 rs7081280 10:104192488 G ENSESTG00000014599 ENSESTT00000036602 Transcript upstream_gene_variant - - - - - - DISTANCE=137 rs7081280 10:104192488 G ENSESTG00000013853 ENSESTT00000034719 Transcript intron_variant - - - - - - rs6584501 10:104209077 T ENSESTG00000014083 ENSESTT00000035222 Transcript upstream_gene_variant - - - - - - DISTANCE=593 rs6584501 10:104209077 T ENSESTG00000013853 ENSESTT00000034683 Transcript intron_variant - - - - - - rs6584501 10:104209077 T ENSESTG00000014083 ENSESTT00000035215 Transcript upstream_gene_variant - - - - - - DISTANCE=533 rs6584501 10:104209077 T CCDS7534.1 CCDS7534.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1137 rs6584501 10:104209077 T 100505761 NR_038937.1 Transcript upstream_gene_variant - - - - - - DISTANCE=497 rs6584501 10:104209077 T ENSESTG00000014083 ENSESTT00000035212 Transcript upstream_gene_variant - - - - - - DISTANCE=520 rs6584501 10:104209077 T 100505761 NR_038938.1 Transcript upstream_gene_variant - - - - - - DISTANCE=497 rs6584501 10:104209077 T 79946 NM_024886.1 Transcript downstream_gene_variant - - - - - - DISTANCE=517 rs6584501 10:104209077 T ENSESTG00000014083 ENSESTT00000035224 Transcript upstream_gene_variant - - - - - - DISTANCE=1234 rs6584501 10:104209077 T ENSESTG00000013853 ENSESTT00000034719 Transcript intron_variant - - - - - - rs7091267 10:104446974 T ENSESTG00000014491 ENSESTT00000036282 Transcript upstream_gene_variant - - - - - - DISTANCE=1309 rs7091267 10:104446974 T ENSESTG00000014476 ENSESTT00000036261 Transcript downstream_gene_variant - - - - - - DISTANCE=2679 rs7091267 10:104446974 T ENSESTG00000014476 ENSESTT00000036266 Transcript downstream_gene_variant - - - - - - DISTANCE=2700 rs7091267 10:104446974 T CCDS7538.1 CCDS7538.1 Transcript intron_variant - - - - - - rs7091267 10:104446974 T 403 NM_004311.3 Transcript intron_variant - - - - - - rs2247722 10:104481642 G CCDS7539.1 CCDS7539.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4752 rs2247722 10:104481642 G ENSESTG00000014252 ENSESTT00000035700 Transcript intron_variant - - - - - - rs2247722 10:104481642 G ENSESTG00000014252 ENSESTT00000035715 Transcript intron_variant - - - - - - rs2247722 10:104481642 G ENSESTG00000014252 ENSESTT00000035708 Transcript intron_variant - - - - - - rs2247722 10:104481642 G 118980 NM_178858.4 Transcript intron_variant - - - - - - rs2247722 10:104481642 G ENSESTG00000014252 ENSESTT00000035723 Transcript intron_variant - - - - - - rs2247722 10:104481642 G ENSESTG00000014252 ENSESTT00000035722 Transcript intron_variant - - - - - - rs2482509 10:104542531 G - ENSR00001426698 RegulatoryFeature regulatory_region_variant - - - - - - rs2482509 10:104542531 G ENSESTG00000014322 ENSESTT00000035862 Transcript intron_variant - - - - - - rs2482509 10:104542531 G 54838 NM_017787.4 Transcript intron_variant - - - - - - rs2482509 10:104542531 G CCDS7540.1 CCDS7540.1 Transcript intron_variant - - - - - - rs2482509 10:104542531 G CCDS44473.1 CCDS44473.1 Transcript intron_variant - - - - - - rs2482509 10:104542531 G 54838 NM_001083913.1 Transcript intron_variant - - - - - - rs284845 10:104557179 C ENSESTG00000014322 ENSESTT00000035862 Transcript intron_variant - - - - - - rs284845 10:104557179 C 54838 NM_017787.4 Transcript intron_variant - - - - - - rs284845 10:104557179 C CCDS7540.1 CCDS7540.1 Transcript intron_variant - - - - - - rs284845 10:104557179 C CCDS44473.1 CCDS44473.1 Transcript intron_variant - - - - - - rs284845 10:104557179 C 54838 NM_001083913.1 Transcript intron_variant - - - - - - rs2148196 10:104864805 T ENSESTG00000018636 ENSESTT00000046996 Transcript intron_variant - - - - - - rs2148196 10:104864805 T 22978 NM_012229.4 Transcript intron_variant - - - - - - rs2148196 10:104864805 T ENSESTG00000018636 ENSESTT00000046987 Transcript downstream_gene_variant - - - - - - DISTANCE=669 rs2148196 10:104864805 T ENSESTG00000018636 ENSESTT00000046927 Transcript intron_variant - - - - - - rs2148196 10:104864805 T ENSESTG00000018636 ENSESTT00000046972 Transcript intron_variant - - - - - - rs2148196 10:104864805 T CCDS7544.1 CCDS7544.1 Transcript intron_variant - - - - - - rs2148196 10:104864805 T ENSESTG00000018636 ENSESTT00000047049 Transcript intron_variant - - - - - - rs2148196 10:104864805 T ENSESTG00000018636 ENSESTT00000047028 Transcript intron_variant - - - - - - rs2148196 10:104864805 T 22978 NM_001134373.2 Transcript intron_variant - - - - - - rs2148196 10:104864805 T ENSESTG00000018636 ENSESTT00000046947 Transcript intron_variant - - - - - - rs2148196 10:104864805 T ENSESTG00000018636 ENSESTT00000047019 Transcript intron_variant - - - - - - rs2209965 10:106298162 T - - - intergenic_variant - - - - - - rs2209969 10:106307600 C - - - intergenic_variant - - - - - - rs7068780 10:106389246 T - - - intergenic_variant - - - - - - rs6584620 10:106391011 C - - - intergenic_variant - - - - - - rs1980910 10:106403583 T 22986 NM_014978.1 Transcript intron_variant - - - - - - rs1980910 10:106403583 T CCDS7558.1 CCDS7558.1 Transcript intron_variant - - - - - - rs4918144 10:106724696 G ENSESTG00000025916 ENSESTT00000065335 Transcript intron_variant - - - - - - rs4918144 10:106724696 G 22986 NM_014978.1 Transcript intron_variant - - - - - - rs4918144 10:106724696 G CCDS7558.1 CCDS7558.1 Transcript intron_variant - - - - - - rs790728 10:106819433 C 22986 NM_014978.1 Transcript intron_variant - - - - - - rs790728 10:106819433 C CCDS7558.1 CCDS7558.1 Transcript intron_variant - - - - - - rs2930465 10:106993001 A ENSESTG00000015014 ENSESTT00000037666 Transcript intron_variant - - - - - - rs2930465 10:106993001 A 22986 NM_014978.1 Transcript intron_variant - - - - - - rs2930465 10:106993001 A CCDS7558.1 CCDS7558.1 Transcript intron_variant - - - - - - rs911573 10:108384883 T - ENSR00000361396 RegulatoryFeature regulatory_region_variant - - - - - - rs911573 10:108384883 T ENSESTG00000032805 ENSESTT00000082927 Transcript intron_variant - - - - - - rs911573 10:108384883 T 114815 NM_001206570.1 Transcript intron_variant - - - - - - rs911573 10:108384883 T 114815 NM_001206572.1 Transcript intron_variant - - - - - - rs911573 10:108384883 T 114815 NM_001206571.1 Transcript intron_variant - - - - - - rs911573 10:108384883 T CCDS7559.1 CCDS7559.1 Transcript intron_variant - - - - - - rs911573 10:108384883 T ENSESTG00000032805 ENSESTT00000082941 Transcript intron_variant - - - - - - rs911573 10:108384883 T ENSESTG00000032805 ENSESTT00000082936 Transcript intron_variant - - - - - - rs911573 10:108384883 T 114815 NM_001013031.2 Transcript intron_variant - - - - - - rs911573 10:108384883 T ENSESTG00000032805 ENSESTT00000082910 Transcript intron_variant - - - - - - rs911573 10:108384883 T ENSESTG00000032805 ENSESTT00000082898 Transcript intron_variant - - - - - - rs911573 10:108384883 T 114815 NM_052918.4 Transcript intron_variant - - - - - - rs911573 10:108384883 T ENSESTG00000032805 ENSESTT00000082904 Transcript intron_variant - - - - - - rs911573 10:108384883 T ENSESTG00000032805 ENSESTT00000082943 Transcript intron_variant - - - - - - rs911573 10:108384883 T CCDS31283.1 CCDS31283.1 Transcript intron_variant - - - - - - rs911573 10:108384883 T ENSESTG00000032805 ENSESTT00000082915 Transcript intron_variant - - - - - - rs911573 10:108384883 T 114815 NM_001206569.1 Transcript intron_variant - - - - - - rs2248044 10:108575191 G CCDS31283.1 CCDS31283.1 Transcript intron_variant - - - - - - rs2248044 10:108575191 G 114815 NM_052918.4 Transcript intron_variant - - - - - - rs2248044 10:108575191 G 114815 NM_001206570.1 Transcript intron_variant - - - - - - rs2248044 10:108575191 G 114815 NM_001206572.1 Transcript intron_variant - - - - - - rs2248044 10:108575191 G 114815 NM_001206571.1 Transcript intron_variant - - - - - - rs2248044 10:108575191 G CCDS7559.1 CCDS7559.1 Transcript intron_variant - - - - - - rs2248044 10:108575191 G 114815 NM_001206569.1 Transcript intron_variant - - - - - - rs2248044 10:108575191 G 114815 NM_001013031.2 Transcript intron_variant - - - - - - rs2248044 10:108575191 G ENSESTG00000032774 ENSESTT00000082848 Transcript intron_variant - - - - - - rs2248044 10:108575191 G ENSESTG00000032774 ENSESTT00000082830 Transcript intron_variant - - - - - - rs1856141 10:109015820 G - - - intergenic_variant - - - - - - rs6584829 10:109547727 C - - - intergenic_variant - - - - - - rs2020020 10:109668086 C - - - intergenic_variant - - - - - - rs10787060 10:109712543 C - ENSR00000361459 RegulatoryFeature regulatory_region_variant - - - - - - rs10787060 10:109712543 C - - - intergenic_variant - - - - - - rs6584874 10:110283478 G - - - intergenic_variant - - - - - - rs7085900 10:110372529 T - - - intergenic_variant - - - - - - rs6584884 10:110475643 A - - - intergenic_variant - - - - - - rs1926569 10:110864782 G ENSESTG00000029500 ENSESTT00000074236 Transcript upstream_gene_variant - - - - - - DISTANCE=1200 rs523358 10:110920121 G - - - intergenic_variant - - - - - - rs10749009 10:111451287 G - - - intergenic_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084247 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084360 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084368 Transcript intron_variant - - - - - - rs1999249 10:111830093 A 120 NM_016824.3 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084318 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084299 Transcript intron_variant - - - - - - rs1999249 10:111830093 A 120 NM_001121.2 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084346 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084241 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084284 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084266 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084304 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084311 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084340 Transcript intron_variant - - - - - - rs1999249 10:111830093 A 120 NM_019903.3 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084274 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084309 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084356 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084321 Transcript intron_variant - - - - - - rs1999249 10:111830093 A ENSESTG00000033317 ENSESTT00000084255 Transcript intron_variant - - - - - - rs10787236 10:112206934 A - ENSR00000361645 RegulatoryFeature regulatory_region_variant - - - - - - rs10787236 10:112206934 A - - - intergenic_variant - - - - - - rs4917568 10:112272807 G - ENSR00000361678 RegulatoryFeature regulatory_region_variant - - - - - - rs4917568 10:112272807 G CCDS7566.1 CCDS7566.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2623 rs4917568 10:112272807 G 1847 NM_004419.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1505 rs12265705 10:112558483 G 282996 NM_001134363.1 Transcript intron_variant - - - - - - rs12265705 10:112558483 G CCDS44477.1 CCDS44477.1 Transcript intron_variant - - - - - - rs10787282 10:112577753 G - ENSR00001017423 RegulatoryFeature regulatory_region_variant - - - - - - rs10787282 10:112577753 G ENSESTG00000033595 ENSESTT00000084918 Transcript upstream_gene_variant - - - - - - DISTANCE=3690 rs10787282 10:112577753 G 282996 NM_001134363.1 Transcript intron_variant - - - - - - rs10787282 10:112577753 G CCDS44477.1 CCDS44477.1 Transcript intron_variant - - - - - - rs1885792 10:112584884 C ENSESTG00000033595 ENSESTT00000084918 Transcript intron_variant - - - - - - rs1885792 10:112584884 C ENSESTG00000033595 ENSESTT00000084927 Transcript upstream_gene_variant - - - - - - DISTANCE=2645 rs1885792 10:112584884 C ENSESTG00000033595 ENSESTT00000084921 Transcript intron_variant - - - - - - rs1885792 10:112584884 C 282996 NM_001134363.1 Transcript intron_variant - - - - - - rs1885792 10:112584884 C CCDS44477.1 CCDS44477.1 Transcript intron_variant - - - - - - rs1969764 10:112608523 C - - - intergenic_variant - - - - - - rs7903401 10:112628100 T - ENSR00001427133 RegulatoryFeature regulatory_region_variant - - - - - - rs7903401 10:112628100 T 27250 NM_001199492.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3453 rs7903401 10:112628100 T ENSESTG00000033863 ENSESTT00000085699 Transcript upstream_gene_variant - - - - - - DISTANCE=3522 rs7903401 10:112628100 T 27250 NM_145341.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3453 rs7903401 10:112628100 T 27250 NM_014456.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3453 rs7903401 10:112628100 T ENSESTG00000033863 ENSESTT00000085710 Transcript upstream_gene_variant - - - - - - DISTANCE=3551 rs7903401 10:112628100 T ENSESTG00000033863 ENSESTT00000085733 Transcript upstream_gene_variant - - - - - - DISTANCE=3569 rs7903401 10:112628100 T 282997 NR_026932.1 Transcript downstream_gene_variant - - - - - - DISTANCE=548 rs10736210 10:112681052 A 92482 NM_001243783.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1928 rs10736210 10:112681052 A CCDS55728.1 CCDS55728.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3137 rs10736210 10:112681052 A 92482 NM_001195307.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1928 rs10736210 10:112681052 A 92482 NM_001195304.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1928 rs10736210 10:112681052 A 92482 NM_001195306.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2358 rs10736210 10:112681052 A ENSESTG00000033964 ENSESTT00000085863 Transcript upstream_gene_variant - - - - - - DISTANCE=2113 rs10736210 10:112681052 A 8036 NM_007373.3 Transcript intron_variant - - - - - - rs10736210 10:112681052 A ENSESTG00000033964 ENSESTT00000085849 Transcript upstream_gene_variant - - - - - - DISTANCE=1928 rs10736210 10:112681052 A CCDS55726.1 CCDS55726.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3137 rs10736210 10:112681052 A ENSESTG00000033938 ENSESTT00000085805 Transcript intron_variant - - - - - - rs10736210 10:112681052 A ENSESTG00000033938 ENSESTT00000085804 Transcript intron_variant - - - - - - rs10736210 10:112681052 A 92482 NM_001195305.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1928 rs10736210 10:112681052 A CCDS55727.1 CCDS55727.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3137 rs7901405 10:112697589 G 644511 NR_026715.1 Transcript upstream_gene_variant - - - - - - DISTANCE=576 rs7901405 10:112697589 G ENSESTG00000033938 ENSESTT00000085805 Transcript intron_variant - - - - - - rs7901405 10:112697589 G ENSESTG00000033938 ENSESTT00000085804 Transcript intron_variant - - - - - - rs7901405 10:112697589 G 8036 NM_007373.3 Transcript intron_variant - - - - - - rs10787297 10:112783380 A ENSESTG00000033958 ENSESTT00000085814 Transcript intron_variant - - - - - - rs1327554 10:112785029 A ENSESTG00000033958 ENSESTT00000085814 Transcript intron_variant - - - - - - rs10749061 10:112956824 A - - - intergenic_variant - - - - - - rs7096547 10:113025638 A - - - intergenic_variant - - - - - - rs3107372 10:113312536 G - - - intergenic_variant - - - - - - rs1562185 10:114450647 C ENSESTG00000013755 ENSESTT00000034329 Transcript intron_variant - - - - - - rs1562185 10:114450647 C ENSESTG00000013738 ENSESTT00000034325 Transcript intron_variant - - - - - - rs1562185 10:114450647 C 143187 NM_145206.2 Transcript intron_variant - - - - - - rs1562185 10:114450647 C CCDS7575.2 CCDS7575.2 Transcript intron_variant - - - - - - rs1562185 10:114450647 C ENSESTG00000013738 ENSESTT00000034308 Transcript intron_variant - - - - - - rs941824 10:114557956 C 143187 NM_145206.2 Transcript intron_variant - - - - - - rs941824 10:114557956 C CCDS7575.2 CCDS7575.2 Transcript intron_variant - - - - - - rs941824 10:114557956 C ENSESTG00000013738 ENSESTT00000034308 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001146274.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001198525.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001146285.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001198527.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001198526.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001198528.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C ENSESTG00000005351 ENSESTT00000013602 Transcript intron_variant - - - - - - rs7075199 10:114772720 C CCDS7576.1 CCDS7576.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C CCDS53577.1 CCDS53577.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_030756.4 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001146284.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001198529.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001198530.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C CCDS55729.1 CCDS55729.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001198531.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001146286.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C 6934 NM_001146283.1 Transcript intron_variant - - - - - - rs7075199 10:114772720 C CCDS53578.1 CCDS53578.1 Transcript intron_variant - - - - - - rs6585213 10:115003479 C - - - intergenic_variant - - - - - - rs238738 10:115731578 G - - - intergenic_variant - - - - - - rs2483572 10:116301570 G - ENSR00001427415 RegulatoryFeature regulatory_region_variant - - - - - - rs2483572 10:116301570 G ENSESTG00000034689 ENSESTT00000087714 Transcript intron_variant - - - - - - rs2483572 10:116301570 G ENSESTG00000034689 ENSESTT00000087743 Transcript intron_variant - - - - - - rs2483572 10:116301570 G 3983 NM_002313.5 Transcript intron_variant - - - - - - rs2483572 10:116301570 G CCDS31288.1 CCDS31288.1 Transcript intron_variant - - - - - - rs2483572 10:116301570 G CCDS7590.1 CCDS7590.1 Transcript intron_variant - - - - - - rs2483572 10:116301570 G 3983 NM_001003407.1 Transcript intron_variant - - - - - - rs2483572 10:116301570 G 3983 NM_001003408.1 Transcript intron_variant - - - - - - rs914939 10:116391991 C - ENSR00001427433 RegulatoryFeature regulatory_region_variant - - - - - - rs914939 10:116391991 C ENSESTG00000034689 ENSESTT00000087714 Transcript intron_variant - - - - - - rs914939 10:116391991 C ENSESTG00000034689 ENSESTT00000087720 Transcript intron_variant - - - - - - rs914939 10:116391991 C ENSESTG00000034689 ENSESTT00000087723 Transcript intron_variant - - - - - - rs914939 10:116391991 C CCDS31288.1 CCDS31288.1 Transcript intron_variant - - - - - - rs914939 10:116391991 C CCDS7590.1 CCDS7590.1 Transcript intron_variant - - - - - - rs914939 10:116391991 C ENSESTG00000034689 ENSESTT00000087727 Transcript 5_prime_UTR_variant 15 - - - - - rs914939 10:116391991 C ENSESTG00000034689 ENSESTT00000087708 Transcript intron_variant - - - - - - rs914939 10:116391991 C 3983 NM_002313.5 Transcript intron_variant - - - - - - rs914939 10:116391991 C ENSESTG00000034689 ENSESTT00000087705 Transcript intron_variant - - - - - - rs914939 10:116391991 C 3983 NM_001003407.1 Transcript intron_variant - - - - - - rs914939 10:116391991 C 3983 NM_001003408.1 Transcript intron_variant - - - - - - rs4751638 10:116434734 A ENSESTG00000034689 ENSESTT00000087714 Transcript intron_variant - - - - - - rs4751638 10:116434734 A ENSESTG00000034689 ENSESTT00000087708 Transcript intron_variant - - - - - - rs4751638 10:116434734 A ENSESTG00000034689 ENSESTT00000087705 Transcript intron_variant - - - - - - rs4751638 10:116434734 A CCDS31288.1 CCDS31288.1 Transcript intron_variant - - - - - - rs4751638 10:116434734 A 3983 NM_001003407.1 Transcript intron_variant - - - - - - rs4751638 10:116434734 A 3983 NM_001003408.1 Transcript intron_variant - - - - - - rs7083240 10:116439864 A ENSESTG00000034689 ENSESTT00000087714 Transcript intron_variant - - - - - - rs7083240 10:116439864 A ENSESTG00000034689 ENSESTT00000087708 Transcript intron_variant - - - - - - rs7083240 10:116439864 A ENSESTG00000034689 ENSESTT00000087705 Transcript intron_variant - - - - - - rs7083240 10:116439864 A CCDS31288.1 CCDS31288.1 Transcript intron_variant - - - - - - rs7083240 10:116439864 A 3983 NM_001003407.1 Transcript intron_variant - - - - - - rs7083240 10:116439864 A 3983 NM_001003408.1 Transcript intron_variant - - - - - - rs10787545 10:116448191 G ENSESTG00000034689 ENSESTT00000087714 Transcript upstream_gene_variant - - - - - - DISTANCE=3791 rs10787545 10:116448191 G ENSESTG00000034689 ENSESTT00000087708 Transcript upstream_gene_variant - - - - - - DISTANCE=3777 rs10787545 10:116448191 G ENSESTG00000034689 ENSESTT00000087705 Transcript upstream_gene_variant - - - - - - DISTANCE=3777 rs10787545 10:116448191 G CCDS31288.1 CCDS31288.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4079 rs10787545 10:116448191 G 3983 NM_001003407.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3777 rs10787545 10:116448191 G 3983 NM_001003408.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3777 rs6421370 10:117278988 C ENSESTG00000007162 ENSESTT00000018098 Transcript intron_variant - - - - - - rs6421370 10:117278988 C CCDS7592.1 CCDS7592.1 Transcript intron_variant - - - - - - rs6421370 10:117278988 C ENSESTG00000007162 ENSESTT00000018121 Transcript intron_variant - - - - - - rs6421370 10:117278988 C 26033 NM_207303.2 Transcript intron_variant - - - - - - rs2490720 10:117386908 T ENSESTG00000007162 ENSESTT00000018126 Transcript intron_variant - - - - - - rs2490720 10:117386908 T CCDS7592.1 CCDS7592.1 Transcript intron_variant - - - - - - rs2490720 10:117386908 T ENSESTG00000007162 ENSESTT00000018121 Transcript intron_variant - - - - - - rs2490720 10:117386908 T 26033 NM_207303.2 Transcript intron_variant - - - - - - rs2960709 10:117522709 C ENSESTG00000007162 ENSESTT00000018126 Transcript intron_variant - - - - - - rs2960709 10:117522709 C CCDS7592.1 CCDS7592.1 Transcript intron_variant - - - - - - rs2960709 10:117522709 C ENSESTG00000007162 ENSESTT00000018121 Transcript intron_variant - - - - - - rs2960709 10:117522709 C 26033 NM_207303.2 Transcript intron_variant - - - - - - rs2960709 10:117522709 C ENSESTG00000007162 ENSESTT00000018128 Transcript intron_variant - - - - - - rs2620954 10:117660854 A ENSESTG00000007162 ENSESTT00000018126 Transcript intron_variant - - - - - - rs2620954 10:117660854 A CCDS7592.1 CCDS7592.1 Transcript intron_variant - - - - - - rs2620954 10:117660854 A ENSESTG00000018500 ENSESTT00000046565 Transcript intron_variant - - - - - - rs2620954 10:117660854 A ENSESTG00000007162 ENSESTT00000018121 Transcript intron_variant - - - - - - rs2620954 10:117660854 A 26033 NM_207303.2 Transcript intron_variant - - - - - - rs2620954 10:117660854 A ENSESTG00000007162 ENSESTT00000018128 Transcript intron_variant - - - - - - rs1637903 10:117801909 C - - - intergenic_variant - - - - - - rs4528233 10:117917054 C CCDS7593.1 CCDS7593.1 Transcript intron_variant - - - - - - rs4528233 10:117917054 C CCDS44481.1 CCDS44481.1 Transcript intron_variant - - - - - - rs4528233 10:117917054 C ENSESTG00000018978 ENSESTT00000047838 Transcript intron_variant - - - - - - rs4528233 10:117917054 C 2674 NM_145793.3 Transcript intron_variant - - - - - - rs4528233 10:117917054 C 2674 NM_005264.4 Transcript intron_variant - - - - - - rs4528233 10:117917054 C ENSESTG00000018978 ENSESTT00000047843 Transcript intron_variant - - - - - - rs4528233 10:117917054 C 2674 NM_001145453.1 Transcript intron_variant - - - - - - rs7069930 10:117923261 G CCDS7593.1 CCDS7593.1 Transcript intron_variant - - - - - - rs7069930 10:117923261 G CCDS44481.1 CCDS44481.1 Transcript intron_variant - - - - - - rs7069930 10:117923261 G ENSESTG00000018978 ENSESTT00000047838 Transcript intron_variant - - - - - - rs7069930 10:117923261 G 2674 NM_145793.3 Transcript intron_variant - - - - - - rs7069930 10:117923261 G 2674 NM_005264.4 Transcript intron_variant - - - - - - rs7069930 10:117923261 G ENSESTG00000018978 ENSESTT00000047843 Transcript intron_variant - - - - - - rs7069930 10:117923261 G 2674 NM_001145453.1 Transcript intron_variant - - - - - - rs11197562 10:117926107 G CCDS7593.1 CCDS7593.1 Transcript intron_variant - - - - - - rs11197562 10:117926107 G CCDS44481.1 CCDS44481.1 Transcript intron_variant - - - - - - rs11197562 10:117926107 G ENSESTG00000018978 ENSESTT00000047838 Transcript intron_variant - - - - - - rs11197562 10:117926107 G 2674 NM_145793.3 Transcript intron_variant - - - - - - rs11197562 10:117926107 G 2674 NM_005264.4 Transcript intron_variant - - - - - - rs11197562 10:117926107 G ENSESTG00000018978 ENSESTT00000047843 Transcript intron_variant - - - - - - rs11197562 10:117926107 G 2674 NM_001145453.1 Transcript intron_variant - - - - - - rs4403730 10:117934757 T CCDS7593.1 CCDS7593.1 Transcript intron_variant - - - - - - rs4403730 10:117934757 T CCDS44481.1 CCDS44481.1 Transcript intron_variant - - - - - - rs4403730 10:117934757 T ENSESTG00000018978 ENSESTT00000047838 Transcript intron_variant - - - - - - rs4403730 10:117934757 T 2674 NM_145793.3 Transcript intron_variant - - - - - - rs4403730 10:117934757 T 2674 NM_005264.4 Transcript intron_variant - - - - - - rs4403730 10:117934757 T ENSESTG00000018978 ENSESTT00000047843 Transcript intron_variant - - - - - - rs4403730 10:117934757 T 2674 NM_001145453.1 Transcript intron_variant - - - - - - rs4237500 10:118204871 G ENSESTG00000018553 ENSESTT00000046678 Transcript downstream_gene_variant - - - - - - DISTANCE=1942 rs4237500 10:118204871 G CCDS31292.1 CCDS31292.1 Transcript intron_variant - - - - - - rs4237500 10:118204871 G 119548 NM_001011709.2 Transcript intron_variant - - - - - - rs3010502 10:118380511 G - ENSR00000362437 RegulatoryFeature regulatory_region_variant - - - - - - rs3010502 10:118380511 G ENSESTG00000018742 ENSESTT00000047272 Transcript intron_variant - - - - - - rs3010502 10:118380511 G ENSESTG00000018742 ENSESTT00000047314 Transcript intron_variant - - - - - - rs3010502 10:118380511 G ENSESTG00000018742 ENSESTT00000047448 Transcript upstream_gene_variant - - - - - - DISTANCE=310 rs3010502 10:118380511 G ENSESTG00000018742 ENSESTT00000047280 Transcript intron_variant - - - - - - rs3010502 10:118380511 G ENSESTG00000018742 ENSESTT00000047325 Transcript intron_variant - - - - - - rs3010502 10:118380511 G ENSESTG00000018742 ENSESTT00000047330 Transcript intron_variant - - - - - - rs3010502 10:118380511 G 5408 NM_005396.4 Transcript intron_variant - - - - - - rs3010502 10:118380511 G ENSESTG00000018742 ENSESTT00000047256 Transcript intron_variant - - - - - - rs1665654 10:118481454 C ENSESTG00000018857 ENSESTT00000047452 Transcript intron_variant - - - - - - rs1665654 10:118481454 C 259217 NM_025015.2 Transcript intron_variant - - - - - - rs1665654 10:118481454 C ENSESTG00000018867 ENSESTT00000047610 Transcript intron_variant - - - - - - rs1665654 10:118481454 C CCDS41569.1 CCDS41569.1 Transcript intron_variant - - - - - - rs1665654 10:118481454 C ENSESTG00000018867 ENSESTT00000047623 Transcript intron_variant - - - - - - rs1638425 10:118481502 A - ENSR00001427578 RegulatoryFeature regulatory_region_variant - - - - - - rs1638425 10:118481502 A ENSESTG00000018857 ENSESTT00000047452 Transcript intron_variant - - - - - - rs1638425 10:118481502 A 259217 NM_025015.2 Transcript intron_variant - - - - - - rs1638425 10:118481502 A ENSESTG00000018867 ENSESTT00000047610 Transcript intron_variant - - - - - - rs1638425 10:118481502 A CCDS41569.1 CCDS41569.1 Transcript intron_variant - - - - - - rs1638425 10:118481502 A ENSESTG00000018867 ENSESTT00000047623 Transcript intron_variant - - - - - - rs1665653 10:118481515 T - ENSR00001427578 RegulatoryFeature regulatory_region_variant - - - - - - rs1665653 10:118481515 T ENSESTG00000018857 ENSESTT00000047452 Transcript intron_variant - - - - - - rs1665653 10:118481515 T 259217 NM_025015.2 Transcript intron_variant - - - - - - rs1665653 10:118481515 T ENSESTG00000018867 ENSESTT00000047610 Transcript intron_variant - - - - - - rs1665653 10:118481515 T CCDS41569.1 CCDS41569.1 Transcript intron_variant - - - - - - rs1665653 10:118481515 T ENSESTG00000018867 ENSESTT00000047623 Transcript intron_variant - - - - - - rs1665660 10:118541323 T - - - intergenic_variant - - - - - - rs1638405 10:118541934 C - - - intergenic_variant - - - - - - rs1867989 10:118543261 G - - - intergenic_variant - - - - - - rs1681733 10:118557427 G - - - intergenic_variant - - - - - - rs1681735 10:118558531 G - - - intergenic_variant - - - - - - rs1681737 10:118560109 G - - - intergenic_variant - - - - - - rs1637561 10:118580164 T - - - intergenic_variant - - - - - - rs1616412 10:118614898 T 387712 NM_001242699.1 Transcript intron_variant - - - - - - rs1681727 10:118625192 C ENSESTG00000017432 ENSESTT00000043890 Transcript intron_variant - - - - - - rs1681727 10:118625192 C 387712 NM_001242699.1 Transcript intron_variant - - - - - - rs1637573 10:118631342 T ENSESTG00000017432 ENSESTT00000043890 Transcript intron_variant - - - - - - rs1637573 10:118631342 T ENSESTG00000017432 ENSESTT00000043936 Transcript upstream_gene_variant - - - - - - DISTANCE=2305 rs1637573 10:118631342 T 387712 NM_001242699.1 Transcript intron_variant - - - - - - rs1637573 10:118631342 T ENSESTG00000017432 ENSESTT00000043947 Transcript upstream_gene_variant - - - - - - DISTANCE=2305 rs1637574 10:118633548 G ENSESTG00000017432 ENSESTT00000043890 Transcript intron_variant - - - - - - rs1637574 10:118633548 G ENSESTG00000017432 ENSESTT00000043936 Transcript upstream_gene_variant - - - - - - DISTANCE=99 rs1637574 10:118633548 G 387712 NM_001242699.1 Transcript intron_variant - - - - - - rs1637574 10:118633548 G ENSESTG00000017432 ENSESTT00000043947 Transcript upstream_gene_variant - - - - - - DISTANCE=99 rs4385806 10:118684653 C ENSESTG00000017715 ENSESTT00000044635 Transcript intron_variant - - - - - - rs4385806 10:118684653 C 57698 NM_018330.6 Transcript intron_variant - - - - - - rs4385806 10:118684653 C 57698 NM_001258298.1 Transcript intron_variant - - - - - - rs4385806 10:118684653 C ENSESTG00000017715 ENSESTT00000044672 Transcript intron_variant - - - - - - rs4385806 10:118684653 C CCDS44482.1 CCDS44482.1 Transcript intron_variant - - - - - - rs4385806 10:118684653 C 57698 NM_001127211.2 Transcript intron_variant - - - - - - rs4385806 10:118684653 C CCDS31293.1 CCDS31293.1 Transcript intron_variant - - - - - - rs4385806 10:118684653 C CCDS58097.1 CCDS58097.1 Transcript intron_variant - - - - - - rs4385806 10:118684653 C 57698 NM_001258299.1 Transcript intron_variant - - - - - - rs4385806 10:118684653 C 57698 NM_001258300.1 Transcript intron_variant - - - - - - rs2576444 10:118723315 A ENSESTG00000017776 ENSESTT00000044880 Transcript intron_variant - - - - - - rs2576444 10:118723315 A ENSESTG00000017715 ENSESTT00000044635 Transcript intron_variant - - - - - - rs2576444 10:118723315 A 57698 NM_018330.6 Transcript intron_variant - - - - - - rs2576444 10:118723315 A 57698 NM_001258298.1 Transcript intron_variant - - - - - - rs2576444 10:118723315 A CCDS44482.1 CCDS44482.1 Transcript intron_variant - - - - - - rs2576444 10:118723315 A 57698 NM_001127211.2 Transcript intron_variant - - - - - - rs2576444 10:118723315 A CCDS31293.1 CCDS31293.1 Transcript intron_variant - - - - - - rs2576444 10:118723315 A CCDS58097.1 CCDS58097.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3582 rs2576444 10:118723315 A 57698 NM_001258299.1 Transcript intron_variant - - - - - - rs2576444 10:118723315 A ENSESTG00000017776 ENSESTT00000044898 Transcript intron_variant - - - - - - rs2576444 10:118723315 A 57698 NM_001258300.1 Transcript intron_variant - - - - - - rs1904301 10:118872190 A 57698 NM_001258300.1 Transcript intron_variant - - - - - - rs7912154 10:118878690 C 57698 NM_001258300.1 Transcript intron_variant - - - - - - rs7906963 10:118883085 C 11023 NM_199131.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4947 rs7906963 10:118883085 C 57698 NM_001258300.1 Transcript intron_variant - - - - - - rs1678051 10:118925377 C - ENSR00000362507 RegulatoryFeature regulatory_region_variant - - - - - - rs1678051 10:118925377 C 100500893 NR_037436.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1812 rs1638439 10:118931440 G 100500893 NR_037436.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4155 rs1678048 10:118937509 G - - - intergenic_variant - - - - - - rs2803811 10:119028122 T CCDS7599.1 CCDS7599.1 Transcript intron_variant - - - - - - rs2803811 10:119028122 T 6571 NM_003054.4 Transcript intron_variant - - - - - - rs2803811 10:119028122 T ENSESTG00000017612 ENSESTT00000044443 Transcript intron_variant - - - - - - rs2803811 10:119028122 T ENSESTG00000017612 ENSESTT00000044419 Transcript downstream_gene_variant - - - - - - DISTANCE=1574 rs7895040 10:120573633 C - - - intergenic_variant - - - - - - rs6585540 10:121001070 A ENSESTG00000011731 ENSESTT00000029518 Transcript intron_variant - - - - - - rs6585540 10:121001070 A ENSESTG00000011731 ENSESTT00000029513 Transcript intron_variant - - - - - - rs6585540 10:121001070 A CCDS7612.1 CCDS7612.1 Transcript intron_variant - - - - - - rs6585540 10:121001070 A 2869 NM_005308.2 Transcript intron_variant - - - - - - rs6585540 10:121001070 A ENSESTG00000011731 ENSESTT00000029424 Transcript intron_variant - - - - - - rs6585540 10:121001070 A ENSESTG00000011731 ENSESTT00000029510 Transcript intron_variant - - - - - - rs11198871 10:121073403 C - ENSR00000644030 RegulatoryFeature regulatory_region_variant - - - - - - rs11198871 10:121073403 C ENSESTG00000011731 ENSESTT00000029518 Transcript intron_variant - - - - - - rs11198871 10:121073403 C ENSESTG00000011731 ENSESTT00000029513 Transcript intron_variant - - - - - - rs11198871 10:121073403 C CCDS7612.1 CCDS7612.1 Transcript intron_variant - - - - - - rs11198871 10:121073403 C 2869 NM_005308.2 Transcript intron_variant - - - - - - rs11198871 10:121073403 C ENSESTG00000011731 ENSESTT00000029424 Transcript intron_variant - - - - - - rs11198871 10:121073403 C ENSESTG00000011731 ENSESTT00000029510 Transcript intron_variant - - - - - - rs4752288 10:121078565 G ENSESTG00000011731 ENSESTT00000029518 Transcript intron_variant - - - - - - rs4752288 10:121078565 G ENSESTG00000011731 ENSESTT00000029513 Transcript intron_variant - - - - - - rs4752288 10:121078565 G CCDS7612.1 CCDS7612.1 Transcript intron_variant - - - - - - rs4752288 10:121078565 G 2869 NM_005308.2 Transcript intron_variant - - - - - - rs4752288 10:121078565 G ENSESTG00000011731 ENSESTT00000029424 Transcript intron_variant - - - - - - rs4752288 10:121078565 G ENSESTG00000011731 ENSESTT00000029510 Transcript intron_variant - - - - - - rs2991767 10:121220796 C - ENSR00001427763 RegulatoryFeature regulatory_region_variant - - - - - - rs2991767 10:121220796 C - - - intergenic_variant - - - - - - rs196224 10:121494335 C ENSESTG00000011811 ENSESTT00000029694 Transcript intron_variant - - - - - - rs196224 10:121494335 C ENSESTG00000011811 ENSESTT00000029696 Transcript intron_variant - - - - - - rs196224 10:121494335 C CCDS7616.1 CCDS7616.1 Transcript intron_variant - - - - - - rs196224 10:121494335 C 22876 NM_001243195.1 Transcript intron_variant - - - - - - rs196224 10:121494335 C 22876 NM_014937.3 Transcript intron_variant - - - - - - rs196224 10:121494335 C ENSESTG00000011811 ENSESTT00000029682 Transcript intron_variant - - - - - - rs196224 10:121494335 C ENSESTG00000011811 ENSESTT00000029695 Transcript intron_variant - - - - - - rs196224 10:121494335 C ENSESTG00000011811 ENSESTT00000029690 Transcript intron_variant - - - - - - rs196204 10:121539894 C ENSESTG00000011811 ENSESTT00000029694 Transcript intron_variant - - - - - - rs196204 10:121539894 C ENSESTG00000011811 ENSESTT00000029696 Transcript intron_variant - - - - - - rs196204 10:121539894 C CCDS7616.1 CCDS7616.1 Transcript intron_variant - - - - - - rs196204 10:121539894 C 22876 NM_001243195.1 Transcript intron_variant - - - - - - rs196204 10:121539894 C 22876 NM_014937.3 Transcript intron_variant - - - - - - rs196204 10:121539894 C ENSESTG00000011811 ENSESTT00000029682 Transcript intron_variant - - - - - - rs196204 10:121539894 C ENSESTG00000011811 ENSESTT00000029695 Transcript intron_variant - - - - - - rs196204 10:121539894 C ENSESTG00000011811 ENSESTT00000029690 Transcript intron_variant - - - - - - rs2456707 10:121622712 T ENSESTG00000026018 ENSESTT00000065754 Transcript intron_variant - - - - - - rs2456707 10:121622712 T 79892 NM_024834.3 Transcript intron_variant - - - - - - rs2456707 10:121622712 T ENSESTG00000026018 ENSESTT00000065805 Transcript intron_variant - - - - - - rs2456707 10:121622712 T CCDS7617.1 CCDS7617.1 Transcript intron_variant - - - - - - rs2456707 10:121622712 T 79892 NM_001256379.1 Transcript intron_variant - - - - - - rs2456707 10:121622712 T ENSESTG00000026018 ENSESTT00000065859 Transcript intron_variant - - - - - - rs2456707 10:121622712 T 79892 NM_001256378.1 Transcript intron_variant - - - - - - rs2456707 10:121622712 T CCDS58099.1 CCDS58099.1 Transcript intron_variant - - - - - - rs2475319 10:121623559 G ENSESTG00000026018 ENSESTT00000065754 Transcript intron_variant - - - - - - rs2475319 10:121623559 G 79892 NM_024834.3 Transcript intron_variant - - - - - - rs2475319 10:121623559 G ENSESTG00000026018 ENSESTT00000065805 Transcript intron_variant - - - - - - rs2475319 10:121623559 G CCDS7617.1 CCDS7617.1 Transcript intron_variant - - - - - - rs2475319 10:121623559 G 79892 NM_001256379.1 Transcript intron_variant - - - - - - rs2475319 10:121623559 G ENSESTG00000026018 ENSESTT00000065859 Transcript intron_variant - - - - - - rs2475319 10:121623559 G 79892 NM_001256378.1 Transcript intron_variant - - - - - - rs2475319 10:121623559 G CCDS58099.1 CCDS58099.1 Transcript intron_variant - - - - - - rs2253818 10:121669759 G 11196 NR_037771.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2253818 10:121669759 G 11196 NM_007190.3 Transcript intron_variant - - - - - - rs2253818 10:121669759 G ENSESTG00000025683 ENSESTT00000065188 Transcript intron_variant - - - - - - rs2253818 10:121669759 G ENSESTG00000025683 ENSESTT00000065172 Transcript intron_variant - - - - - - rs2253818 10:121669759 G CCDS7618.1 CCDS7618.1 Transcript intron_variant - - - - - - rs2901227 10:122103719 G - - - intergenic_variant - - - - - - rs2463125 10:122195512 T - - - intergenic_variant - - - - - - rs2912788 10:123324464 A CCDS44485.1 CCDS44485.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A ENSESTG00000027311 ENSESTT00000068776 Transcript intron_variant - - - - - - rs2912788 10:123324464 A CCDS53584.1 CCDS53584.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A CCDS44488.1 CCDS44488.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_001144913.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A ENSESTG00000027113 ENSESTT00000068723 Transcript intron_variant - - - - - - rs2912788 10:123324464 A ENSESTG00000027113 ENSESTT00000068744 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_000141.4 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_001144917.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_001144915.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A CCDS31298.1 CCDS31298.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A CCDS44486.1 CCDS44486.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NR_073009.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2912788 10:123324464 A CCDS44489.1 CCDS44489.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_001144918.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_022970.3 Transcript intron_variant - - - - - - rs2912788 10:123324464 A ENSESTG00000027113 ENSESTT00000068560 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_001144919.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A ENSESTG00000027113 ENSESTT00000068729 Transcript intron_variant - - - - - - rs2912788 10:123324464 A ENSESTG00000027113 ENSESTT00000068646 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_001144914.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A ENSESTG00000027113 ENSESTT00000068661 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_001144916.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A ENSESTG00000027113 ENSESTT00000068736 Transcript intron_variant - - - - - - rs2912788 10:123324464 A CCDS7620.2 CCDS7620.2 Transcript intron_variant - - - - - - rs2912788 10:123324464 A CCDS44487.1 CCDS44487.1 Transcript intron_variant - - - - - - rs2912788 10:123324464 A 2263 NM_023029.2 Transcript intron_variant - - - - - - rs10732823 10:123653853 T ENSESTG00000014445 ENSESTT00000036192 Transcript intron_variant - - - - - - rs10732823 10:123653853 T CCDS31300.1 CCDS31300.1 Transcript intron_variant - - - - - - rs10732823 10:123653853 T CCDS31299.1 CCDS31299.1 Transcript intron_variant - - - - - - rs10732823 10:123653853 T ENSESTG00000027052 ENSESTT00000068175 Transcript intron_variant - - - - - - rs10732823 10:123653853 T 11101 NM_007041.2 Transcript intron_variant - - - - - - rs10732823 10:123653853 T ENSESTG00000014445 ENSESTT00000036188 Transcript intron_variant - - - - - - rs10732823 10:123653853 T ENSESTG00000014445 ENSESTT00000036184 Transcript intron_variant - - - - - - rs10732823 10:123653853 T ENSESTG00000027052 ENSESTT00000068203 Transcript intron_variant - - - - - - rs10732823 10:123653853 T 11101 NM_001001976.1 Transcript intron_variant - - - - - - rs7099895 10:123716730 A - ENSR00000363102 RegulatoryFeature regulatory_region_variant - - - - - - rs7099895 10:123716730 A 54780 NM_017615.2 Transcript 3_prime_UTR_variant 1278 - - - - - rs7099895 10:123716730 A ENSESTG00000014165 ENSESTT00000035438 Transcript intron_variant - - - - - - rs7099895 10:123716730 A 54780 NM_001167865.1 Transcript 3_prime_UTR_variant 1275 - - - - - rs7099895 10:123716730 A CCDS7624.1 CCDS7624.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2121 rs7099895 10:123716730 A ENSESTG00000014426 ENSESTT00000036148 Transcript 3_prime_UTR_variant 548 - - - - - rs11200552 10:124080174 T 118663 NM_144587.2 Transcript intron_variant - - - - - - rs11200552 10:124080174 T CCDS31301.1 CCDS31301.1 Transcript intron_variant - - - - - - rs77915873 10:124996271 C ENSESTG00000024778 ENSESTT00000062801 Transcript intron_variant - - - - - - rs77915873 10:124996271 C ENSESTG00000024778 ENSESTT00000062737 Transcript intron_variant - - - - - - rs9422298 10:125709174 C ENSESTG00000033117 ENSESTT00000083674 Transcript upstream_gene_variant - - - - - - DISTANCE=1789 rs4529855 10:127046097 G - - - intergenic_variant - - - - - - rs927955 10:127376118 T - ENSR00000363651 RegulatoryFeature regulatory_region_variant - - - - - - rs927955 10:127376118 T ENSESTG00000025096 ENSESTT00000063317 Transcript upstream_gene_variant - - - - - - DISTANCE=4405 rs927955 10:127376118 T 283038 NR_033848.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs927955 10:127376118 T CCDS44493.1 CCDS44493.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4560 rs927955 10:127376118 T ENSESTG00000025096 ENSESTT00000063326 Transcript upstream_gene_variant - - - - - - DISTANCE=4443 rs927955 10:127376118 T 387718 NM_001128202.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4405 rs927955 10:127376118 T ENSESTG00000024307 ENSESTT00000061476 Transcript intron_variant - - - - - - rs927955 10:127376118 T ENSESTG00000024307 ENSESTT00000061459 Transcript intron_variant - - - - - - rs2366889 10:128415105 A ENSESTG00000003304 ENSESTT00000008235 Transcript intron_variant - - - - - - rs2366890 10:128415893 A ENSESTG00000003304 ENSESTT00000008235 Transcript intron_variant - - - - - - rs7090523 10:128478121 G ENSESTG00000003304 ENSESTT00000008235 Transcript intron_variant - - - - - - rs4491136 10:128490735 A ENSESTG00000003304 ENSESTT00000008235 Transcript upstream_gene_variant - - - - - - DISTANCE=3458 rs4246199 10:128522012 T 728065 XM_001126459.1 Transcript intron_variant - - - - - - rs4411214 10:128534795 C 728065 XM_001126459.1 Transcript intron_variant - - - - - - rs4480450 10:128559168 T 728065 XM_001126459.1 Transcript intron_variant - - - - - - rs2486965 10:128922064 C ENSESTG00000017876 ENSESTT00000045364 Transcript intron_variant - - - - - - rs2486965 10:128922064 C 1793 NM_001380.3 Transcript intron_variant - - - - - - rs2486965 10:128922064 C ENSESTG00000017876 ENSESTT00000045305 Transcript intron_variant - - - - - - rs2486965 10:128922064 C ENSESTG00000017876 ENSESTT00000045457 Transcript intron_variant - - - - - - rs2486965 10:128922064 C ENSESTG00000017876 ENSESTT00000045319 Transcript intron_variant - - - - - - rs2486965 10:128922064 C ENSESTG00000017876 ENSESTT00000045472 Transcript intron_variant - - - - - - rs2489393 10:128942998 A CCDS31312.1 CCDS31312.1 Transcript intron_variant - - - - - - rs2489393 10:128942998 A ENSESTG00000018201 ENSESTT00000045832 Transcript intron_variant - - - - - - rs2489393 10:128942998 A 1793 NM_001380.3 Transcript intron_variant - - - - - - rs2489393 10:128942998 A 642938 NM_001039762.2 Transcript intron_variant - - - - - - rs2489393 10:128942998 A ENSESTG00000017876 ENSESTT00000045457 Transcript intron_variant - - - - - - rs2489393 10:128942998 A ENSESTG00000017876 ENSESTT00000045472 Transcript intron_variant - - - - - - rs1892136 10:128951525 A - ENSR00001428374 RegulatoryFeature regulatory_region_variant - - - - - - rs1892136 10:128951525 A CCDS31312.1 CCDS31312.1 Transcript intron_variant - - - - - - rs1892136 10:128951525 A ENSESTG00000018201 ENSESTT00000045832 Transcript intron_variant - - - - - - rs1892136 10:128951525 A 1793 NM_001380.3 Transcript intron_variant - - - - - - rs1892136 10:128951525 A 642938 NM_001039762.2 Transcript intron_variant - - - - - - rs1892136 10:128951525 A ENSESTG00000017876 ENSESTT00000045457 Transcript intron_variant - - - - - - rs1892136 10:128951525 A ENSESTG00000017876 ENSESTT00000045472 Transcript intron_variant - - - - - - rs2483866 10:128998004 T 1793 NM_001380.3 Transcript intron_variant - - - - - - rs2483866 10:128998004 T 642938 NM_001039762.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3582 rs2483866 10:128998004 T ENSESTG00000017876 ENSESTT00000045457 Transcript intron_variant - - - - - - rs2483866 10:128998004 T ENSESTG00000017876 ENSESTT00000045472 Transcript intron_variant - - - - - - rs2483866 10:128998004 T ENSESTG00000018194 ENSESTT00000045819 Transcript upstream_gene_variant - - - - - - DISTANCE=3582 rs7091688 10:129145250 G 1793 NM_001380.3 Transcript intron_variant - - - - - - rs7091688 10:129145250 G ENSESTG00000017876 ENSESTT00000045457 Transcript intron_variant - - - - - - rs10734118 10:129746074 C 5791 NM_006504.4 Transcript intron_variant - - - - - - rs10734118 10:129746074 C ENSESTG00000027198 ENSESTT00000068547 Transcript intron_variant - - - - - - rs4350282 10:129867815 C - ENSR00000363914 RegulatoryFeature regulatory_region_variant - - - - - - rs4350282 10:129867815 C - MA0139.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=2;MOTIF_NAME=Jaspar_Matrix_CTCF:MA0139.1;HIGH_INF_POS=N;MOTIF_SCORE_CHANGE=0.012 rs4350282 10:129867815 C ENSESTG00000027198 ENSESTT00000068786 Transcript intron_variant - - - - - - rs4350282 10:129867815 C ENSESTG00000027198 ENSESTT00000068794 Transcript intron_variant - - - - - - rs4350282 10:129867815 C CCDS7658.1 CCDS7658.1 Transcript intron_variant - - - - - - rs4350282 10:129867815 C 5791 NM_130435.3 Transcript intron_variant - - - - - - rs4350282 10:129867815 C 5791 NM_006504.4 Transcript intron_variant - - - - - - rs4350282 10:129867815 C ENSESTG00000027198 ENSESTT00000068821 Transcript intron_variant - - - - - - rs4350282 10:129867815 C ENSESTG00000027198 ENSESTT00000068836 Transcript upstream_gene_variant - - - - - - DISTANCE=746 rs4350282 10:129867815 C CCDS7657.1 CCDS7657.1 Transcript intron_variant - - - - - - rs4350282 10:129867815 C ENSESTG00000027198 ENSESTT00000068826 Transcript upstream_gene_variant - - - - - - DISTANCE=707 rs4350282 10:129867815 C ENSESTG00000027198 ENSESTT00000068852 Transcript upstream_gene_variant - - - - - - DISTANCE=2320 rs10741143 10:129887524 G 5791 NM_130435.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3344 rs10741143 10:129887524 G 5791 NM_006504.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3344 rs2032030 10:130128770 T - - - intergenic_variant - - - - - - rs1936424 10:130150600 C - - - intergenic_variant - - - - - - rs10764773 10:130161439 G - - - intergenic_variant - - - - - - rs946533 10:130260341 G - - - intergenic_variant - - - - - - rs7905050 10:130265535 C - - - intergenic_variant - - - - - - rs7901732 10:130265572 C - - - intergenic_variant - - - - - - rs7081953 10:130268926 C - - - intergenic_variant - - - - - - rs7904066 10:130311808 G - - - intergenic_variant - - - - - - rs7083637 10:130318296 G ENSESTG00000027367 ENSESTT00000068912 Transcript downstream_gene_variant - - - - - - DISTANCE=3215 rs10829424 10:130345952 G - - - intergenic_variant - - - - - - rs2123415 10:130844898 C - ENSR00000363971 RegulatoryFeature regulatory_region_variant - - - - - - rs2123415 10:130844898 C - - - intergenic_variant - - - - - - rs1452877 10:130922033 C - - - intergenic_variant - - - - - - rs1762459 10:131227522 G - - - intergenic_variant - - - - - - rs1711648 10:131269291 T CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs1711648 10:131269291 T ENSESTG00000001404 ENSESTT00000003323 Transcript intron_variant - - - - - - rs1711648 10:131269291 T ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs1711648 10:131269291 T ENSESTG00000001404 ENSESTT00000003301 Transcript intron_variant - - - - - - rs1711648 10:131269291 T 4255 NM_002412.3 Transcript intron_variant - - - - - - rs1762424 10:131284161 G CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs1762424 10:131284161 G ENSESTG00000001404 ENSESTT00000003323 Transcript intron_variant - - - - - - rs1762424 10:131284161 G ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs1762424 10:131284161 G ENSESTG00000001404 ENSESTT00000003301 Transcript intron_variant - - - - - - rs1762424 10:131284161 G 4255 NM_002412.3 Transcript intron_variant - - - - - - rs1537687 10:131314057 G CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs1537687 10:131314057 G ENSESTG00000001404 ENSESTT00000003323 Transcript intron_variant - - - - - - rs1537687 10:131314057 G ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs1537687 10:131314057 G ENSESTG00000001404 ENSESTT00000003301 Transcript intron_variant - - - - - - rs1537687 10:131314057 G 4255 NM_002412.3 Transcript intron_variant - - - - - - rs570883 10:131353532 C CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs570883 10:131353532 C ENSESTG00000001404 ENSESTT00000003323 Transcript intron_variant - - - - - - rs570883 10:131353532 C ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs570883 10:131353532 C 4255 NM_002412.3 Transcript intron_variant - - - - - - rs488269 10:131386052 T CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs488269 10:131386052 T ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs488269 10:131386052 T 4255 NM_002412.3 Transcript intron_variant - - - - - - rs492549 10:131405015 A CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs492549 10:131405015 A ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs492549 10:131405015 A 4255 NM_002412.3 Transcript intron_variant - - - - - - rs511110 10:131406210 A CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs511110 10:131406210 A ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs511110 10:131406210 A 4255 NM_002412.3 Transcript intron_variant - - - - - - rs495614 10:131419775 A CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs495614 10:131419775 A ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs495614 10:131419775 A 4255 NM_002412.3 Transcript intron_variant - - - - - - rs538879 10:131420015 G CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs538879 10:131420015 G ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs538879 10:131420015 G 4255 NM_002412.3 Transcript intron_variant - - - - - - rs516862 10:131424357 G CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs516862 10:131424357 G ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs516862 10:131424357 G 4255 NM_002412.3 Transcript intron_variant - - - - - - rs510224 10:131424778 G - ENSR00000364009 RegulatoryFeature regulatory_region_variant - - - - - - rs510224 10:131424778 G CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs510224 10:131424778 G ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs510224 10:131424778 G 4255 NM_002412.3 Transcript intron_variant - - - - - - rs478477 10:131429101 G CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs478477 10:131429101 G ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs478477 10:131429101 G 4255 NM_002412.3 Transcript intron_variant - - - - - - rs474937 10:131429454 C - ENSR00001428467 RegulatoryFeature regulatory_region_variant - - - - - - rs474937 10:131429454 C CCDS7660.2 CCDS7660.2 Transcript intron_variant - - - - - - rs474937 10:131429454 C ENSESTG00000001404 ENSESTT00000003319 Transcript intron_variant - - - - - - rs474937 10:131429454 C 4255 NM_002412.3 Transcript intron_variant - - - - - - rs1547175 10:131572903 G - - - intergenic_variant - - - - - - rs680383 10:131883315 A 387723 NR_034125.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs635849 10:132109273 G - - - intergenic_variant - - - - - - rs2921906 10:132481494 T - - - intergenic_variant - - - - - - rs2397323 10:132511526 C - - - intergenic_variant - - - - - - rs2397461 10:132534246 G - - - intergenic_variant - - - - - - rs3097971 10:132756572 G 100422867 NR_036180.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4279 rs2918168 10:133036738 G 256536 NM_174937.3 Transcript intron_variant - - - - - - rs2918168 10:133036738 G CCDS7662.2 CCDS7662.2 Transcript intron_variant - - - - - - rs6420799 10:133470050 A - - - intergenic_variant - - - - - - rs9419696 10:133515703 G - - - intergenic_variant - - - - - - rs4411222 10:133761763 A - ENSR00000364172 RegulatoryFeature regulatory_region_variant - - - - - - rs4411222 10:133761763 A 55844 NM_018461.3 Transcript intron_variant - - - - - - rs4411222 10:133761763 A 55844 NR_033191.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4411222 10:133761763 A ENSESTG00000028292 ENSESTT00000071205 Transcript intron_variant - - - - - - rs7917223 10:133910638 G - - - intergenic_variant - - - - - - rs2814194 10:134042407 C ENSESTG00000028794 ENSESTT00000072500 Transcript intron_variant - - - - - - rs2814194 10:134042407 C ENSESTG00000028794 ENSESTT00000072638 Transcript intron_variant - - - - - - rs2814194 10:134042407 C ENSESTG00000028794 ENSESTT00000072469 Transcript intron_variant - - - - - - rs2814194 10:134042407 C 282974 NM_173575.2 Transcript intron_variant - - - - - - rs2814194 10:134042407 C ENSESTG00000028794 ENSESTT00000072689 Transcript intron_variant - - - - - - rs2814194 10:134042407 C CCDS7666.1 CCDS7666.1 Transcript intron_variant - - - - - - rs2814194 10:134042407 C ENSESTG00000028794 ENSESTT00000072618 Transcript intron_variant - - - - - - rs2814194 10:134042407 C ENSESTG00000028794 ENSESTT00000072493 Transcript intron_variant - - - - - - rs2814194 10:134042407 C ENSESTG00000028794 ENSESTT00000072519 Transcript intron_variant - - - - - - rs2767439 10:134616338 A - ENSR00000364362 RegulatoryFeature regulatory_region_variant - - - - - - rs2767439 10:134616338 A - - - intergenic_variant - - - - - - rs4838704 10:134988703 G ENSESTG00000012538 ENSESTT00000031428 Transcript intron_variant - - - - - - rs4838704 10:134988703 G ENSESTG00000012538 ENSESTT00000031440 Transcript intron_variant - - - - - - rs4838704 10:134988703 G ENSESTG00000012538 ENSESTT00000031429 Transcript downstream_gene_variant - - - - - - DISTANCE=1203 rs4838704 10:134988703 G CCDS7674.1 CCDS7674.1 Transcript intron_variant - - - - - - rs4838704 10:134988703 G ENSESTG00000012538 ENSESTT00000031431 Transcript intron_variant - - - - - - rs4838704 10:134988703 G 85442 NM_152643.6 Transcript intron_variant - - - - - - rs2995309 10:135081684 C - ENSR00000364466 RegulatoryFeature regulatory_region_variant - - - - - - rs2995309 10:135081684 C CCDS58102.1 CCDS58102.1 Transcript intron_variant - - - - - - rs2995309 10:135081684 C CCDS58103.1 CCDS58103.1 Transcript intron_variant - - - - - - rs2995309 10:135081684 C 101 NM_001164489.1 Transcript intron_variant - - - - - - rs2995309 10:135081684 C 101 NM_001164490.1 Transcript intron_variant - - - - - - rs2995309 10:135081684 C 101 NM_001109.4 Transcript intron_variant - - - - - - rs2995309 10:135081684 C ENSESTG00000012855 ENSESTT00000032238 Transcript intron_variant - - - - - - rs10745293 10:135145821 G ENSESTG00000012821 ENSESTT00000032167 Transcript intron_variant - - - - - - rs10745293 10:135145821 G ENSESTG00000012599 ENSESTT00000031597 Transcript upstream_gene_variant - - - - - - DISTANCE=2589 rs10745293 10:135145821 G ENSESTG00000012821 ENSESTT00000032170 Transcript intron_variant - - - - - - rs10745293 10:135145821 G CCDS7678.1 CCDS7678.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3328 rs10745293 10:135145821 G 50632 NM_015722.3 Transcript intron_variant - - - - - - rs7395065 11:433387 G ENSESTG00000023120 ENSESTT00000058428 Transcript missense_variant 360 277 93 F/L Ttc/Ctc - rs7395065 11:433387 G 338440 NM_001012302.2 Transcript missense_variant 362 277 93 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs7395065 11:433387 G CCDS31326.1 CCDS31326.1 Transcript missense_variant 277 277 93 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs7395065 11:433387 G ENSESTG00000023120 ENSESTT00000058478 Transcript intron_variant - - - - - - rs7395065 11:433387 G ENSESTG00000023172 ENSESTT00000058613 Transcript upstream_gene_variant - - - - - - DISTANCE=4637 rs7395065 11:433387 G ENSESTG00000023120 ENSESTT00000058413 Transcript missense_variant 360 277 93 F/L Ttc/Ctc - rs7395065 11:433387 G ENSESTG00000023120 ENSESTT00000058446 Transcript missense_variant 360 277 93 F/L Ttc/Ctc - rs7395065 11:433387 G ENSESTG00000023172 ENSESTT00000058587 Transcript upstream_gene_variant - - - - - - DISTANCE=3204 rs7395065 11:433387 G ENSESTG00000023172 ENSESTT00000058560 Transcript upstream_gene_variant - - - - - - DISTANCE=3204 rs7395065 11:433387 G ENSESTG00000021040 ENSESTT00000052798 Transcript downstream_gene_variant - - - - - - DISTANCE=4559 rs28498399 11:726178 C - ENSR00000187027 RegulatoryFeature regulatory_region_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054052 Transcript downstream_gene_variant - - - - - - DISTANCE=4124 rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054147 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054134 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054192 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054084 Transcript downstream_gene_variant - - - - - - DISTANCE=4124 rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054113 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054069 Transcript downstream_gene_variant - - - - - - DISTANCE=4124 rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000053994 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054043 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054140 Transcript downstream_gene_variant - - - - - - DISTANCE=4124 rs28498399 11:726178 C 64787 NM_022772.3 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C CCDS31328.1 CCDS31328.1 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054006 Transcript downstream_gene_variant - - - - - - DISTANCE=4124 rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054128 Transcript intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054076 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054164 Transcript downstream_gene_variant - - - - - - DISTANCE=3678 rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054063 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000021411 ENSESTT00000054175 Transcript splice_region_variant,intron_variant - - - - - - rs28498399 11:726178 C ENSESTG00000022730 ENSESTT00000057331 Transcript intron_variant - - - - - - rs9328567 11:1015183 T 161 NM_001242837.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2938 rs9328567 11:1015183 T 4588 NM_005961.2 Transcript intron_variant - - - - - - rs9328567 11:1015183 T ENSESTG00000022171 ENSESTT00000056256 Transcript downstream_gene_variant - - - - - - DISTANCE=4360 rs9328567 11:1015183 T ENSESTG00000022171 ENSESTT00000056163 Transcript downstream_gene_variant - - - - - - DISTANCE=4360 rs9328567 11:1015183 T CCDS44513.1 CCDS44513.1 Transcript intron_variant - - - - - - rs9328567 11:1015183 T CCDS44512.1 CCDS44512.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4558 rs9328567 11:1015183 T ENSESTG00000022171 ENSESTT00000056172 Transcript downstream_gene_variant - - - - - - DISTANCE=4360 rs9328567 11:1015183 T ENSESTG00000022171 ENSESTT00000056222 Transcript downstream_gene_variant - - - - - - DISTANCE=4360 rs9328567 11:1015183 T ENSESTG00000022171 ENSESTT00000056193 Transcript downstream_gene_variant - - - - - - DISTANCE=4360 rs9328567 11:1015183 T 161 NM_012305.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2938 rs9328567 11:1015183 T ENSESTG00000022171 ENSESTT00000055955 Transcript downstream_gene_variant - - - - - - DISTANCE=4360 rs9328567 11:1015183 T ENSESTG00000022171 ENSESTT00000056289 Transcript downstream_gene_variant - - - - - - DISTANCE=4360 rs9794913 11:1015445 G 161 NM_001242837.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3200 rs9794913 11:1015445 G 4588 NM_005961.2 Transcript intron_variant - - - - - - rs9794913 11:1015445 G ENSESTG00000022171 ENSESTT00000056256 Transcript downstream_gene_variant - - - - - - DISTANCE=4622 rs9794913 11:1015445 G ENSESTG00000022171 ENSESTT00000056163 Transcript downstream_gene_variant - - - - - - DISTANCE=4622 rs9794913 11:1015445 G CCDS44513.1 CCDS44513.1 Transcript intron_variant - - - - - - rs9794913 11:1015445 G CCDS44512.1 CCDS44512.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4820 rs9794913 11:1015445 G ENSESTG00000022171 ENSESTT00000056172 Transcript downstream_gene_variant - - - - - - DISTANCE=4622 rs9794913 11:1015445 G ENSESTG00000022171 ENSESTT00000056222 Transcript downstream_gene_variant - - - - - - DISTANCE=4622 rs9794913 11:1015445 G ENSESTG00000022171 ENSESTT00000056193 Transcript downstream_gene_variant - - - - - - DISTANCE=4622 rs9794913 11:1015445 G 161 NM_012305.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3200 rs9794913 11:1015445 G ENSESTG00000022171 ENSESTT00000055955 Transcript downstream_gene_variant - - - - - - DISTANCE=4622 rs9794913 11:1015445 G ENSESTG00000022171 ENSESTT00000056289 Transcript downstream_gene_variant - - - - - - DISTANCE=4622 rs11245977 11:1131914 A - - - intergenic_variant - - - - - - rs10839956 11:1300915 C ENSESTG00000007835 ENSESTT00000019882 Transcript intron_variant - - - - - - rs10839956 11:1300915 C 54472 NM_019009.3 Transcript intron_variant - - - - - - rs10839956 11:1300915 C CCDS7723.1 CCDS7723.1 Transcript intron_variant - - - - - - rs10839956 11:1300915 C ENSESTG00000007835 ENSESTT00000019869 Transcript intron_variant - - - - - - rs10839956 11:1300915 C ENSESTG00000007835 ENSESTT00000019876 Transcript downstream_gene_variant - - - - - - DISTANCE=3854 rs10839956 11:1300915 C ENSESTG00000007835 ENSESTT00000019891 Transcript intron_variant - - - - - - rs10839956 11:1300915 C ENSESTG00000007835 ENSESTT00000019820 Transcript intron_variant - - - - - - rs10839956 11:1300915 C ENSESTG00000007835 ENSESTT00000019887 Transcript intron_variant - - - - - - rs10832358 11:1372018 T - - - intergenic_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018931 Transcript intron_variant - - - - - - rs7397027 11:1440252 A 9024 NM_001256630.1 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018927 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018916 Transcript intron_variant - - - - - - rs7397027 11:1440252 A CCDS58107.1 CCDS58107.1 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018924 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018934 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018939 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018832 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018821 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018871 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018884 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018824 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018863 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018846 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018873 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018908 Transcript intron_variant - - - - - - rs7397027 11:1440252 A CCDS58106.1 CCDS58106.1 Transcript intron_variant - - - - - - rs7397027 11:1440252 A 9024 NR_046332.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018898 Transcript intron_variant - - - - - - rs7397027 11:1440252 A 9024 NR_046331.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018920 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018784 Transcript intron_variant - - - - - - rs7397027 11:1440252 A 9024 NM_001256627.1 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018875 Transcript intron_variant - - - - - - rs7397027 11:1440252 A 9024 NM_003957.3 Transcript intron_variant - - - - - - rs7397027 11:1440252 A CCDS58108.1 CCDS58108.1 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018813 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018909 Transcript intron_variant - - - - - - rs7397027 11:1440252 A CCDS41590.1 CCDS41590.1 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018888 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018904 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018852 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018829 Transcript intron_variant - - - - - - rs7397027 11:1440252 A 9024 NM_001256629.1 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018893 Transcript intron_variant - - - - - - rs7397027 11:1440252 A ENSESTG00000007452 ENSESTT00000018882 Transcript intron_variant - - - - - - rs504493 11:1864661 C - ENSR00000557180 RegulatoryFeature regulatory_region_variant - - - - - - rs504493 11:1864661 C ENSESTG00000007592 ENSESTT00000019125 Transcript downstream_gene_variant - - - - - - DISTANCE=1754 rs504493 11:1864661 C ENSESTG00000007592 ENSESTT00000019114 Transcript downstream_gene_variant - - - - - - DISTANCE=1751 rs504493 11:1864661 C 7136 NM_001145841.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1751 rs504493 11:1864661 C CCDS53594.1 CCDS53594.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1880 rs504493 11:1864661 C 7136 NM_003282.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1751 rs504493 11:1864661 C ENSESTG00000007592 ENSESTT00000019122 Transcript downstream_gene_variant - - - - - - DISTANCE=1754 rs504493 11:1864661 C 7136 NM_001145829.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1751 rs504493 11:1864661 C CCDS31333.1 CCDS31333.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1880 rs504493 11:1864661 C ENSESTG00000007592 ENSESTT00000019109 Transcript downstream_gene_variant - - - - - - DISTANCE=1754 rs9667646 11:1951478 C 7140 NM_001042781.2 Transcript intron_variant - - - - - - rs9667646 11:1951478 C ENSESTG00000007688 ENSESTT00000019411 Transcript upstream_gene_variant - - - - - - DISTANCE=4630 rs9667646 11:1951478 C CCDS7727.1 CCDS7727.1 Transcript intron_variant - - - - - - rs9667646 11:1951478 C CCDS41594.1 CCDS41594.1 Transcript intron_variant - - - - - - rs9667646 11:1951478 C CCDS41595.1 CCDS41595.1 Transcript intron_variant - - - - - - rs9667646 11:1951478 C 7140 NM_006757.3 Transcript intron_variant - - - - - - rs9667646 11:1951478 C 7140 NM_001042782.2 Transcript intron_variant - - - - - - rs9667646 11:1951478 C CCDS41596.1 CCDS41596.1 Transcript intron_variant - - - - - - rs9667646 11:1951478 C ENSESTG00000007688 ENSESTT00000019408 Transcript upstream_gene_variant - - - - - - DISTANCE=2218 rs9667646 11:1951478 C 7140 NM_001042780.2 Transcript intron_variant - - - - - - rs9667646 11:1951478 C ENSESTG00000007688 ENSESTT00000019406 Transcript intron_variant - - - - - - rs10734659 11:2193511 G 7054 NM_000360.3 Transcript upstream_gene_variant - - - - - - DISTANCE=476 rs10734659 11:2193511 G 7054 NM_199293.2 Transcript upstream_gene_variant - - - - - - DISTANCE=476 rs10734659 11:2193511 G CCDS7730.1 CCDS7730.1 Transcript upstream_gene_variant - - - - - - DISTANCE=495 rs10734659 11:2193511 G CCDS31338.1 CCDS31338.1 Transcript upstream_gene_variant - - - - - - DISTANCE=495 rs10734659 11:2193511 G 100616126 NR_039834.1 Transcript upstream_gene_variant - - - - - - DISTANCE=782 rs10734659 11:2193511 G 7054 NM_199292.2 Transcript upstream_gene_variant - - - - - - DISTANCE=476 rs10734659 11:2193511 G ENSESTG00000032324 ENSESTT00000081626 Transcript upstream_gene_variant - - - - - - DISTANCE=2484 rs10734659 11:2193511 G ENSESTG00000032324 ENSESTT00000081609 Transcript upstream_gene_variant - - - - - - DISTANCE=2484 rs10734659 11:2193511 G CCDS7731.1 CCDS7731.1 Transcript upstream_gene_variant - - - - - - DISTANCE=495 rs9651665 11:2229577 G - - - intergenic_variant - - - - - - rs455775 11:2780974 C 3784 NM_000218.2 Transcript intron_variant - - - - - - rs455775 11:2780974 C 3784 NR_040711.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs455775 11:2780974 C ENSESTG00000032016 ENSESTT00000080937 Transcript intron_variant - - - - - - rs455775 11:2780974 C ENSESTG00000032016 ENSESTT00000080906 Transcript intron_variant - - - - - - rs455775 11:2780974 C ENSESTG00000032016 ENSESTT00000080872 Transcript intron_variant - - - - - - rs455775 11:2780974 C CCDS7736.1 CCDS7736.1 Transcript intron_variant - - - - - - rs231874 11:2785296 C - ENSR00000317083 RegulatoryFeature regulatory_region_variant - - - - - - rs231874 11:2785296 C 3784 NM_000218.2 Transcript intron_variant - - - - - - rs231874 11:2785296 C 3784 NR_040711.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs231874 11:2785296 C ENSESTG00000032016 ENSESTT00000080937 Transcript intron_variant - - - - - - rs231874 11:2785296 C ENSESTG00000032016 ENSESTT00000080906 Transcript intron_variant - - - - - - rs231874 11:2785296 C ENSESTG00000032016 ENSESTT00000080872 Transcript intron_variant - - - - - - rs231874 11:2785296 C CCDS7736.1 CCDS7736.1 Transcript intron_variant - - - - - - rs163176 11:2837243 A 3784 NM_000218.2 Transcript intron_variant - - - - - - rs163176 11:2837243 A 3784 NR_040711.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs163176 11:2837243 A ENSESTG00000032016 ENSESTT00000080937 Transcript intron_variant - - - - - - rs163176 11:2837243 A ENSESTG00000032016 ENSESTT00000080906 Transcript intron_variant - - - - - - rs163176 11:2837243 A ENSESTG00000032016 ENSESTT00000080872 Transcript intron_variant - - - - - - rs163176 11:2837243 A CCDS7736.1 CCDS7736.1 Transcript intron_variant - - - - - - rs163179 11:2841217 C 3784 NM_000218.2 Transcript intron_variant - - - - - - rs163179 11:2841217 C 3784 NR_040711.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs163179 11:2841217 C ENSESTG00000032016 ENSESTT00000080937 Transcript intron_variant - - - - - - rs163179 11:2841217 C ENSESTG00000032016 ENSESTT00000080906 Transcript intron_variant - - - - - - rs163179 11:2841217 C ENSESTG00000032016 ENSESTT00000080872 Transcript intron_variant - - - - - - rs163179 11:2841217 C CCDS7736.1 CCDS7736.1 Transcript intron_variant - - - - - - rs2532983 11:2931282 G ENSESTG00000032099 ENSESTT00000081109 Transcript downstream_gene_variant - - - - - - DISTANCE=802 rs2532983 11:2931282 G CCDS7740.1 CCDS7740.1 Transcript intron_variant - - - - - - rs2532983 11:2931282 G 5002 NM_183233.2 Transcript intron_variant - - - - - - rs2532983 11:2931282 G ENSESTG00000032099 ENSESTT00000081100 Transcript intron_variant - - - - - - rs2532983 11:2931282 G 5002 NM_002555.5 Transcript intron_variant - - - - - - rs7124230 11:3120135 G CCDS31344.1 CCDS31344.1 Transcript intron_variant - - - - - - rs7124230 11:3120135 G 114879 NM_001144063.1 Transcript intron_variant - - - - - - rs7124230 11:3120135 G 114879 NM_020896.3 Transcript intron_variant - - - - - - rs7124230 11:3120135 G ENSESTG00000032305 ENSESTT00000081590 Transcript downstream_gene_variant - - - - - - DISTANCE=4364 rs7124230 11:3120135 G CCDS31343.1 CCDS31343.1 Transcript intron_variant - - - - - - rs7124230 11:3120135 G 114879 NM_145638.2 Transcript intron_variant - - - - - - rs10833236 11:3121934 C CCDS31344.1 CCDS31344.1 Transcript intron_variant - - - - - - rs10833236 11:3121934 C 114879 NM_001144063.1 Transcript intron_variant - - - - - - rs10833236 11:3121934 C 114879 NM_020896.3 Transcript intron_variant - - - - - - rs10833236 11:3121934 C ENSESTG00000032305 ENSESTT00000081590 Transcript downstream_gene_variant - - - - - - DISTANCE=2565 rs10833236 11:3121934 C CCDS31343.1 CCDS31343.1 Transcript intron_variant - - - - - - rs10833236 11:3121934 C 114879 NM_145638.2 Transcript intron_variant - - - - - - rs4445613 11:3129805 G CCDS31344.1 CCDS31344.1 Transcript intron_variant - - - - - - rs4445613 11:3129805 G ENSESTG00000032305 ENSESTT00000081604 Transcript intron_variant - - - - - - rs4445613 11:3129805 G ENSESTG00000032305 ENSESTT00000081562 Transcript intron_variant - - - - - - rs4445613 11:3129805 G ENSESTG00000032305 ENSESTT00000081630 Transcript intron_variant - - - - - - rs4445613 11:3129805 G 114879 NM_145638.2 Transcript intron_variant - - - - - - rs4445613 11:3129805 G ENSESTG00000032305 ENSESTT00000081666 Transcript intron_variant - - - - - - rs4445613 11:3129805 G ENSESTG00000032305 ENSESTT00000081645 Transcript intron_variant - - - - - - rs4445613 11:3129805 G 114879 NM_001144063.1 Transcript intron_variant - - - - - - rs4445613 11:3129805 G 114879 NM_020896.3 Transcript intron_variant - - - - - - rs4445613 11:3129805 G ENSESTG00000032305 ENSESTT00000081590 Transcript intron_variant - - - - - - rs4445613 11:3129805 G ENSESTG00000032305 ENSESTT00000081567 Transcript intron_variant - - - - - - rs4445613 11:3129805 G ENSESTG00000032305 ENSESTT00000081661 Transcript intron_variant - - - - - - rs4445613 11:3129805 G CCDS31343.1 CCDS31343.1 Transcript intron_variant - - - - - - rs7394846 11:3246157 G ENSESTG00000032010 ENSESTT00000080783 Transcript downstream_gene_variant - - - - - - DISTANCE=3050 rs7394846 11:3246157 G CCDS41603.1 CCDS41603.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2934 rs7394846 11:3246157 G 283303 NR_027138.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1796 rs7394846 11:3246157 G 116534 NM_001039165.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2884 rs7394846 11:3246157 G ENSESTG00000032010 ENSESTT00000080775 Transcript downstream_gene_variant - - - - - - DISTANCE=2949 rs6578352 11:3448620 C - - - intergenic_variant - - - - - - rs12293905 11:3676062 G - ENSR00000317188 RegulatoryFeature regulatory_region_variant - - - - - - rs12293905 11:3676062 G 417 NM_004314.2 Transcript intron_variant - - - - - - rs12293905 11:3676062 G CCDS7744.1 CCDS7744.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4382 rs2599738 11:3765344 T ENSESTG00000032201 ENSESTT00000081371 Transcript intron_variant - - - - - - rs2599738 11:3765344 T ENSESTG00000032201 ENSESTT00000081353 Transcript intron_variant - - - - - - rs2599738 11:3765344 T ENSESTG00000032201 ENSESTT00000081306 Transcript intron_variant - - - - - - rs2599738 11:3765344 T CCDS41605.1 CCDS41605.1 Transcript intron_variant - - - - - - rs2599738 11:3765344 T CCDS41606.1 CCDS41606.1 Transcript intron_variant - - - - - - rs2599738 11:3765344 T CCDS31347.1 CCDS31347.1 Transcript intron_variant - - - - - - rs2599738 11:3765344 T ENSESTG00000032201 ENSESTT00000081383 Transcript intron_variant - - - - - - rs2599738 11:3765344 T CCDS7746.1 CCDS7746.1 Transcript intron_variant - - - - - - rs2599738 11:3765344 T 4928 NM_016320.4 Transcript intron_variant - - - - - - rs2599738 11:3765344 T 4928 NM_139131.3 Transcript intron_variant - - - - - - rs2599738 11:3765344 T ENSESTG00000032201 ENSESTT00000081388 Transcript intron_variant - - - - - - rs2599738 11:3765344 T 4928 NM_005387.5 Transcript intron_variant - - - - - - rs2599738 11:3765344 T 4928 NM_139132.3 Transcript intron_variant - - - - - - rs4910583 11:3889635 C CCDS7749.1 CCDS7749.1 Transcript intron_variant - - - - - - rs4910583 11:3889635 C ENSESTG00000032137 ENSESTT00000081180 Transcript intron_variant - - - - - - rs4910583 11:3889635 C ENSESTG00000032137 ENSESTT00000081191 Transcript intron_variant - - - - - - rs4910583 11:3889635 C 6786 NM_003156.3 Transcript intron_variant - - - - - - rs4910583 11:3889635 C ENSESTG00000032137 ENSESTT00000081171 Transcript intron_variant - - - - - - rs4910583 11:3889635 C ENSESTG00000032137 ENSESTT00000081125 Transcript intron_variant - - - - - - rs10430938 11:3932167 G CCDS7749.1 CCDS7749.1 Transcript intron_variant - - - - - - rs10430938 11:3932167 G ENSESTG00000032137 ENSESTT00000081180 Transcript intron_variant - - - - - - rs10430938 11:3932167 G 6786 NM_003156.3 Transcript intron_variant - - - - - - rs10430938 11:3932167 G ENSESTG00000032137 ENSESTT00000081125 Transcript intron_variant - - - - - - rs10430938 11:3932167 G ENSESTG00000032137 ENSESTT00000081208 Transcript intron_variant - - - - - - rs10430938 11:3932167 G ENSESTG00000032137 ENSESTT00000081191 Transcript intron_variant - - - - - - rs10430938 11:3932167 G ENSESTG00000032137 ENSESTT00000081171 Transcript intron_variant - - - - - - rs10430938 11:3932167 G ENSESTG00000032137 ENSESTT00000081216 Transcript intron_variant - - - - - - rs2412337 11:3972815 T - ENSR00001051842 RegulatoryFeature regulatory_region_variant - - - - - - rs2412337 11:3972815 T CCDS7749.1 CCDS7749.1 Transcript intron_variant - - - - - - rs2412337 11:3972815 T ENSESTG00000032137 ENSESTT00000081180 Transcript intron_variant - - - - - - rs2412337 11:3972815 T 6786 NM_003156.3 Transcript intron_variant - - - - - - rs2412337 11:3972815 T ENSESTG00000032137 ENSESTT00000081125 Transcript intron_variant - - - - - - rs2412337 11:3972815 T ENSESTG00000032137 ENSESTT00000081208 Transcript intron_variant - - - - - - rs2412337 11:3972815 T ENSESTG00000032137 ENSESTT00000081191 Transcript intron_variant - - - - - - rs2412337 11:3972815 T ENSESTG00000032137 ENSESTT00000081171 Transcript intron_variant - - - - - - rs2412337 11:3972815 T ENSESTG00000032137 ENSESTT00000081229 Transcript intron_variant - - - - - - rs2412337 11:3972815 T ENSESTG00000032137 ENSESTT00000081216 Transcript intron_variant - - - - - - rs2412337 11:3972815 T ENSESTG00000032137 ENSESTT00000081224 Transcript intron_variant - - - - - - rs442979 11:4328600 C - - - intergenic_variant - - - - - - rs2709163 11:4539723 A - - - intergenic_variant - - - - - - rs7111884 11:4587663 T 143501 NM_144663.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4990 rs7111884 11:4587663 T CCDS31354.1 CCDS31354.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4990 rs10768115 11:4637669 T - - - intergenic_variant - - - - - - rs1032447 11:4721621 C ENSESTG00000035407 ENSESTT00000089421 Transcript upstream_gene_variant - - - - - - DISTANCE=2537 rs1032447 11:4721621 C ENSESTG00000035407 ENSESTT00000089427 Transcript upstream_gene_variant - - - - - - DISTANCE=2545 rs1032447 11:4721621 C 81285 NM_030774.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2545 rs10734443 11:4758120 A - - - intergenic_variant - - - - - - rs6578541 11:5026108 T - ENSR00000557617 RegulatoryFeature regulatory_region_variant - - - - - - rs6578541 11:5026108 T 119682 NM_001004755.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4948 rs6578541 11:5026108 T CCDS31369.1 CCDS31369.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4948 rs1597974 11:5859446 T 390078 NM_001005167.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2740 rs1597974 11:5859446 T CCDS53597.1 CCDS53597.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2740 rs4438015 11:5950033 C - - - intergenic_variant - - - - - - rs7125937 11:6076147 G - - - intergenic_variant - - - - - - rs325658 11:6160129 A - - - intergenic_variant - - - - - - rs4505045 11:6194486 G 255725 NM_001004052.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2930 rs4505045 11:6194486 G CCDS53598.1 CCDS53598.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2930 rs192986 11:6199656 G - - - intergenic_variant - - - - - - rs2682105 11:6378917 C ENSESTG00000002665 ENSESTT00000006647 Transcript intron_variant - - - - - - rs10742975 11:6590840 G ENSESTG00000002436 ENSESTT00000006061 Transcript intron_variant - - - - - - rs10742975 11:6590840 G CCDS44532.1 CCDS44532.1 Transcript intron_variant - - - - - - rs10742975 11:6590840 G 144132 NM_144666.2 Transcript intron_variant - - - - - - rs10742975 11:6590840 G ENSESTG00000002436 ENSESTT00000006057 Transcript intron_variant - - - - - - rs10742975 11:6590840 G ENSESTG00000002591 ENSESTT00000006417 Transcript intron_variant - - - - - - rs10742975 11:6590840 G ENSESTG00000002457 ENSESTT00000006081 Transcript upstream_gene_variant - - - - - - DISTANCE=1767 rs10742975 11:6590840 G ENSESTG00000002436 ENSESTT00000006065 Transcript downstream_gene_variant - - - - - - DISTANCE=2749 rs10742975 11:6590840 G ENSESTG00000002436 ENSESTT00000006052 Transcript intron_variant - - - - - - rs10742975 11:6590840 G ENSESTG00000002436 ENSESTT00000006070 Transcript downstream_gene_variant - - - - - - DISTANCE=2749 rs10742975 11:6590840 G ENSESTG00000002436 ENSESTT00000006051 Transcript intron_variant - - - - - - rs7124284 11:6595569 G ENSESTG00000002436 ENSESTT00000006061 Transcript downstream_gene_variant - - - - - - DISTANCE=4177 rs7124284 11:6595569 G CCDS44532.1 CCDS44532.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2353 rs7124284 11:6595569 G 144132 NM_144666.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2314 rs7124284 11:6595569 G ENSESTG00000002436 ENSESTT00000006057 Transcript downstream_gene_variant - - - - - - DISTANCE=4177 rs7124284 11:6595569 G ENSESTG00000002591 ENSESTT00000006417 Transcript intron_variant - - - - - - rs7124284 11:6595569 G ENSESTG00000002457 ENSESTT00000006081 Transcript downstream_gene_variant - - - - - - DISTANCE=2012 rs7124284 11:6595569 G ENSESTG00000002436 ENSESTT00000006052 Transcript downstream_gene_variant - - - - - - DISTANCE=3350 rs7124284 11:6595569 G ENSESTG00000002436 ENSESTT00000006051 Transcript downstream_gene_variant - - - - - - DISTANCE=3350 rs10769703 11:6673686 T 8642 NM_003737.2 Transcript intron_variant - - - - - - rs3116373 11:6918170 G CCDS31416.1 CCDS31416.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4439 rs3116373 11:6918170 G 120776 NM_003700.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4439 rs4758174 11:7350619 G CCDS7778.1 CCDS7778.1 Transcript intron_variant - - - - - - rs4758174 11:7350619 G ENSESTG00000012011 ENSESTT00000030100 Transcript intron_variant - - - - - - rs4758174 11:7350619 G ENSESTG00000012011 ENSESTT00000030102 Transcript intron_variant - - - - - - rs4758174 11:7350619 G 143425 NM_175733.3 Transcript intron_variant - - - - - - rs1487852 11:7354959 G CCDS7778.1 CCDS7778.1 Transcript intron_variant - - - - - - rs1487852 11:7354959 G ENSESTG00000012011 ENSESTT00000030100 Transcript intron_variant - - - - - - rs1487852 11:7354959 G ENSESTG00000012011 ENSESTT00000030102 Transcript intron_variant - - - - - - rs1487852 11:7354959 G 143425 NM_175733.3 Transcript intron_variant - - - - - - rs4758181 11:7433538 C CCDS7778.1 CCDS7778.1 Transcript intron_variant - - - - - - rs4758181 11:7433538 C ENSESTG00000012011 ENSESTT00000030100 Transcript intron_variant - - - - - - rs4758181 11:7433538 C ENSESTG00000012011 ENSESTT00000030102 Transcript intron_variant - - - - - - rs4758181 11:7433538 C 143425 NM_175733.3 Transcript intron_variant - - - - - - rs10743022 11:7437951 T CCDS7778.1 CCDS7778.1 Transcript intron_variant - - - - - - rs10743022 11:7437951 T ENSESTG00000012011 ENSESTT00000030100 Transcript downstream_gene_variant - - - - - - DISTANCE=635 rs10743022 11:7437951 T ENSESTG00000012018 ENSESTT00000030110 Transcript upstream_gene_variant - - - - - - DISTANCE=1344 rs10743022 11:7437951 T ENSESTG00000012011 ENSESTT00000030102 Transcript downstream_gene_variant - - - - - - DISTANCE=654 rs10743022 11:7437951 T 143425 NM_175733.3 Transcript intron_variant - - - - - - rs1320044 11:7444818 G ENSESTG00000012173 ENSESTT00000030460 Transcript downstream_gene_variant - - - - - - DISTANCE=4002 rs1320044 11:7444818 G CCDS7778.1 CCDS7778.1 Transcript intron_variant - - - - - - rs1320044 11:7444818 G ENSESTG00000012018 ENSESTT00000030110 Transcript intron_variant - - - - - - rs1320044 11:7444818 G 143425 NM_175733.3 Transcript intron_variant - - - - - - rs10128732 11:7539102 G 8495 NM_003621.3 Transcript intron_variant - - - - - - rs10128732 11:7539102 G ENSESTG00000012077 ENSESTT00000030247 Transcript intron_variant - - - - - - rs10128732 11:7539102 G ENSESTG00000012077 ENSESTT00000030235 Transcript intron_variant - - - - - - rs10128732 11:7539102 G ENSESTG00000012077 ENSESTT00000030254 Transcript intron_variant - - - - - - rs4543980 11:8026029 G - - - intergenic_variant - - - - - - rs7111853 11:8036574 T ENSESTG00000003247 ENSESTT00000008073 Transcript upstream_gene_variant - - - - - - DISTANCE=4217 rs7131581 11:8036606 C ENSESTG00000003247 ENSESTT00000008073 Transcript upstream_gene_variant - - - - - - DISTANCE=4185 rs7481825 11:8130925 A 79608 NM_024557.4 Transcript 3_prime_UTR_variant 2481 - - - - - rs7481825 11:8130925 A 7275 NM_003320.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3271 rs7481825 11:8130925 A ENSESTG00000003260 ENSESTT00000008087 Transcript intron_variant - - - - - - rs7481825 11:8130925 A ENSESTG00000003374 ENSESTT00000008465 Transcript downstream_gene_variant - - - - - - DISTANCE=1400 rs7481825 11:8130925 A ENSESTG00000003374 ENSESTT00000008442 Transcript downstream_gene_variant - - - - - - DISTANCE=1684 rs7481825 11:8130925 A 79608 NM_001206672.2 Transcript 3_prime_UTR_variant 2241 - - - - - rs7481825 11:8130925 A 79608 NR_045405.1 Transcript non_coding_exon_variant,nc_transcript_variant 2533 - - - - - rs7481825 11:8130925 A CCDS55741.1 CCDS55741.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1320 rs7481825 11:8130925 A 79608 NM_001135109.2 Transcript 3_prime_UTR_variant 1938 - - - - - rs7481825 11:8130925 A CCDS7788.1 CCDS7788.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1320 rs7481825 11:8130925 A 7275 NM_177972.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3271 rs7481825 11:8130925 A 79608 NM_001206671.2 Transcript 3_prime_UTR_variant 2484 - - - - - rs7481825 11:8130925 A ENSESTG00000003374 ENSESTT00000008436 Transcript downstream_gene_variant - - - - - - DISTANCE=1341 rs7481825 11:8130925 A ENSESTG00000003374 ENSESTT00000008463 Transcript downstream_gene_variant - - - - - - DISTANCE=1650 rs7481825 11:8130925 A CCDS44533.1 CCDS44533.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1320 rs7481825 11:8130925 A CCDS55742.1 CCDS55742.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1320 rs10743063 11:8232597 A - - - intergenic_variant - - - - - - rs4758060 11:8339575 C - - - intergenic_variant - - - - - - rs10769904 11:8374601 C - ENSR00001567941 RegulatoryFeature regulatory_region_variant - - - - - - rs10769904 11:8374601 C - - - intergenic_variant - - - - - - rs7103339 11:9524700 A ENSESTG00000018620 ENSESTT00000047018 Transcript intron_variant - - - - - - rs7103339 11:9524700 A ENSESTG00000018620 ENSESTT00000046998 Transcript intron_variant - - - - - - rs7103339 11:9524700 A 7702 NM_003442.5 Transcript intron_variant - - - - - - rs7103339 11:9524700 A ENSESTG00000018620 ENSESTT00000047013 Transcript intron_variant - - - - - - rs7103339 11:9524700 A CCDS7799.2 CCDS7799.2 Transcript intron_variant - - - - - - rs7103339 11:9524700 A ENSESTG00000018620 ENSESTT00000046990 Transcript intron_variant - - - - - - rs4910478 11:9586335 G - - - intergenic_variant - - - - - - rs7480519 11:9736081 C ENSESTG00000018759 ENSESTT00000047425 Transcript intron_variant - - - - - - rs7480519 11:9736081 C 23075 NM_015055.2 Transcript intron_variant - - - - - - rs7480519 11:9736081 C ENSESTG00000018759 ENSESTT00000047403 Transcript intron_variant - - - - - - rs7480519 11:9736081 C CCDS31426.1 CCDS31426.1 Transcript intron_variant - - - - - - rs7480519 11:9736081 C ENSESTG00000018759 ENSESTT00000047421 Transcript intron_variant - - - - - - rs7480519 11:9736081 C ENSESTG00000018759 ENSESTT00000047398 Transcript intron_variant - - - - - - rs360138 11:9774681 C - ENSR00001568050 RegulatoryFeature regulatory_region_variant - - - - - - rs360138 11:9774681 C 23075 NM_015055.2 Transcript downstream_gene_variant - - - - - - DISTANCE=173 rs360138 11:9774681 C ENSESTG00000018759 ENSESTT00000047398 Transcript downstream_gene_variant - - - - - - DISTANCE=2400 rs360138 11:9774681 C ENSESTG00000018759 ENSESTT00000047425 Transcript downstream_gene_variant - - - - - - DISTANCE=2400 rs360138 11:9774681 C ENSESTG00000018759 ENSESTT00000047443 Transcript downstream_gene_variant - - - - - - DISTANCE=2400 rs360138 11:9774681 C CCDS31426.1 CCDS31426.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3164 rs360138 11:9774681 C 440028 NR_033972.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1636 rs360138 11:9774681 C ENSESTG00000018759 ENSESTT00000047421 Transcript downstream_gene_variant - - - - - - DISTANCE=2400 rs360138 11:9774681 C ENSESTG00000018759 ENSESTT00000047438 Transcript downstream_gene_variant - - - - - - DISTANCE=2400 rs12791485 11:9807270 G ENSESTG00000018901 ENSESTT00000047743 Transcript downstream_gene_variant - - - - - - DISTANCE=3383 rs12791485 11:9807270 G ENSESTG00000018856 ENSESTT00000047498 Transcript intron_variant - - - - - - rs12791485 11:9807270 G ENSESTG00000018856 ENSESTT00000047513 Transcript intron_variant - - - - - - rs12791485 11:9807270 G CCDS31427.1 CCDS31427.1 Transcript intron_variant - - - - - - rs12791485 11:9807270 G ENSESTG00000018856 ENSESTT00000047460 Transcript intron_variant - - - - - - rs12791485 11:9807270 G 81846 NM_030962.3 Transcript intron_variant - - - - - - rs12791485 11:9807270 G ENSESTG00000018856 ENSESTT00000047485 Transcript intron_variant - - - - - - rs12791485 11:9807270 G 283104 NR_036485.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs12791485 11:9807270 G ENSESTG00000018901 ENSESTT00000047696 Transcript downstream_gene_variant - - - - - - DISTANCE=3383 rs12791485 11:9807270 G ENSESTG00000018901 ENSESTT00000047690 Transcript downstream_gene_variant - - - - - - DISTANCE=3383 rs12791485 11:9807270 G ENSESTG00000018856 ENSESTT00000047472 Transcript downstream_gene_variant - - - - - - DISTANCE=2613 rs10458868 11:10222363 A 81846 NM_030962.3 Transcript intron_variant - - - - - - rs10458868 11:10222363 A ENSESTG00000031022 ENSESTT00000078104 Transcript intron_variant - - - - - - rs10458868 11:10222363 A ENSESTG00000031022 ENSESTT00000078116 Transcript intron_variant - - - - - - rs10458868 11:10222363 A CCDS31427.1 CCDS31427.1 Transcript intron_variant - - - - - - rs10840387 11:10313750 T - ENSR00001568095 RegulatoryFeature regulatory_region_variant - - - - - - rs10840387 11:10313750 T 81846 NM_030962.3 Transcript intron_variant - - - - - - rs10840387 11:10313750 T ENSESTG00000031022 ENSESTT00000078104 Transcript intron_variant - - - - - - rs10840387 11:10313750 T ENSESTG00000031022 ENSESTT00000078116 Transcript intron_variant - - - - - - rs10840387 11:10313750 T CCDS31427.1 CCDS31427.1 Transcript intron_variant - - - - - - rs10743142 11:10508150 G 272 NM_000480.2 Transcript intron_variant - - - - - - rs10743142 11:10508150 G ENSESTG00000030350 ENSESTT00000076509 Transcript intron_variant - - - - - - rs10743142 11:10508150 G CCDS44537.1 CCDS44537.1 Transcript intron_variant - - - - - - rs10743142 11:10508150 G 272 NM_001172431.1 Transcript intron_variant - - - - - - rs10743142 11:10508150 G CCDS53601.1 CCDS53601.1 Transcript intron_variant - - - - - - rs10743142 11:10508150 G 272 NM_001025389.1 Transcript intron_variant - - - - - - rs10743142 11:10508150 G ENSESTG00000030350 ENSESTT00000076523 Transcript intron_variant - - - - - - rs10743142 11:10508150 G ENSESTG00000030350 ENSESTT00000076449 Transcript intron_variant - - - - - - rs10743142 11:10508150 G ENSESTG00000030350 ENSESTT00000076586 Transcript intron_variant - - - - - - rs10743142 11:10508150 G 272 NM_001025390.1 Transcript intron_variant - - - - - - rs10743142 11:10508150 G 272 NM_001172430.1 Transcript intron_variant - - - - - - rs10743142 11:10508150 G CCDS7802.1 CCDS7802.1 Transcript intron_variant - - - - - - rs10743142 11:10508150 G ENSESTG00000030350 ENSESTT00000076565 Transcript downstream_gene_variant - - - - - - DISTANCE=4505 rs10743142 11:10508150 G ENSESTG00000030350 ENSESTT00000076623 Transcript intron_variant - - - - - - rs10743142 11:10508150 G ENSESTG00000030350 ENSESTT00000076490 Transcript downstream_gene_variant - - - - - - DISTANCE=4504 rs10743142 11:10508150 G CCDS41617.1 CCDS41617.1 Transcript intron_variant - - - - - - rs4910188 11:10784317 G ENSESTG00000030540 ENSESTT00000077054 Transcript intron_variant - - - - - - rs4910188 11:10784317 G ENSESTG00000030617 ENSESTT00000077204 Transcript upstream_gene_variant - - - - - - DISTANCE=3564 rs4910188 11:10784317 G CCDS7805.1 CCDS7805.1 Transcript intron_variant - - - - - - rs4910188 11:10784317 G 9646 NM_014633.3 Transcript intron_variant - - - - - - rs7116920 11:10893973 C ENSESTG00000030686 ENSESTT00000077259 Transcript intron_variant - - - - - - rs7116920 11:10893973 C 729013 NR_034137.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7116920 11:10893973 C ENSESTG00000030686 ENSESTT00000077246 Transcript intron_variant - - - - - - rs1486543 11:11043020 C - - - intergenic_variant - - - - - - rs965371 11:11046016 C - - - intergenic_variant - - - - - - rs1386151 11:11047163 C - - - intergenic_variant - - - - - - rs7931718 11:11055258 A - - - intergenic_variant - - - - - - rs2403371 11:11064059 A - - - intergenic_variant - - - - - - rs7927781 11:11074614 G - - - intergenic_variant - - - - - - rs10741537 11:11265144 G - - - intergenic_variant - - - - - - rs7395405 11:11457344 C 374378 NM_198516.2 Transcript intron_variant - - - - - - rs7395405 11:11457344 C CCDS7807.1 CCDS7807.1 Transcript intron_variant - - - - - - rs7395405 11:11457344 C ENSESTG00000016387 ENSESTT00000041119 Transcript intron_variant - - - - - - rs6484912 11:11461459 G 374378 NM_198516.2 Transcript intron_variant - - - - - - rs6484912 11:11461459 G CCDS7807.1 CCDS7807.1 Transcript intron_variant - - - - - - rs6484912 11:11461459 G ENSESTG00000016387 ENSESTT00000041119 Transcript intron_variant - - - - - - rs10466377 11:11464769 A 374378 NM_198516.2 Transcript intron_variant - - - - - - rs10466377 11:11464769 A CCDS7807.1 CCDS7807.1 Transcript intron_variant - - - - - - rs10466377 11:11464769 A ENSESTG00000016387 ENSESTT00000041119 Transcript intron_variant - - - - - - rs7107602 11:11476297 C - ENSR00000558494 RegulatoryFeature regulatory_region_variant - - - - - - rs7107602 11:11476297 C 374378 NM_198516.2 Transcript intron_variant - - - - - - rs7107602 11:11476297 C CCDS7807.1 CCDS7807.1 Transcript intron_variant - - - - - - rs7107602 11:11476297 C ENSESTG00000016387 ENSESTT00000041119 Transcript intron_variant - - - - - - rs10765852 11:11476858 T 374378 NM_198516.2 Transcript intron_variant - - - - - - rs10765852 11:11476858 T CCDS7807.1 CCDS7807.1 Transcript intron_variant - - - - - - rs10765852 11:11476858 T ENSESTG00000016387 ENSESTT00000041119 Transcript intron_variant - - - - - - rs4756768 11:12121177 A - ENSR00000317687 RegulatoryFeature regulatory_region_variant - - - - - - rs4756768 11:12121177 A - - - intergenic_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060872 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060689 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060839 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060732 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060617 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060538 Transcript intron_variant - - - - - - rs2706659 11:12275961 G CCDS7809.1 CCDS7809.1 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060868 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060795 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060772 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060509 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060664 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060704 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060683 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060555 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060571 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060840 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060586 Transcript intron_variant - - - - - - rs2706659 11:12275961 G 9645 NM_014632.2 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060755 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060784 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060650 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060599 Transcript intron_variant - - - - - - rs2706659 11:12275961 G ENSESTG00000023883 ENSESTT00000060743 Transcript intron_variant - - - - - - rs7109678 11:12495623 C ENSESTG00000024133 ENSESTT00000061061 Transcript intron_variant - - - - - - rs7109678 11:12495623 C ENSESTG00000024442 ENSESTT00000061798 Transcript upstream_gene_variant - - - - - - DISTANCE=287 rs7109678 11:12495623 C ENSESTG00000024133 ENSESTT00000061133 Transcript upstream_gene_variant - - - - - - DISTANCE=3766 rs7109678 11:12495623 C ENSESTG00000024133 ENSESTT00000061073 Transcript intron_variant - - - - - - rs7109678 11:12495623 C CCDS44541.2 CCDS44541.2 Transcript intron_variant - - - - - - rs7109678 11:12495623 C ENSESTG00000024133 ENSESTT00000061000 Transcript downstream_gene_variant - - - - - - DISTANCE=104 rs7109678 11:12495623 C 55742 NM_018222.4 Transcript intron_variant - - - - - - rs7109678 11:12495623 C ENSESTG00000024133 ENSESTT00000061141 Transcript upstream_gene_variant - - - - - - DISTANCE=3766 rs7109678 11:12495623 C ENSESTG00000024133 ENSESTT00000061081 Transcript intron_variant - - - - - - rs3927025 11:12816488 G ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs3927025 11:12816488 G ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs3927025 11:12816488 G 7003 NM_021961.5 Transcript intron_variant - - - - - - rs3927025 11:12816488 G CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs10741603 11:12822328 A ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs10741603 11:12822328 A ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs10741603 11:12822328 A 7003 NM_021961.5 Transcript intron_variant - - - - - - rs10741603 11:12822328 A CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs9888152 11:12825521 C ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs9888152 11:12825521 C ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs9888152 11:12825521 C 7003 NM_021961.5 Transcript intron_variant - - - - - - rs9888152 11:12825521 C CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs1530176 11:12833089 C ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs1530176 11:12833089 C ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs1530176 11:12833089 C 7003 NM_021961.5 Transcript intron_variant - - - - - - rs1530176 11:12833089 C CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs10765995 11:12850836 C - ENSR00000558802 RegulatoryFeature regulatory_region_variant - - - - - - rs10765995 11:12850836 C ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs10765995 11:12850836 C ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs10765995 11:12850836 C ENSESTG00000024379 ENSESTT00000061785 Transcript intron_variant - - - - - - rs10765995 11:12850836 C 7003 NM_021961.5 Transcript intron_variant - - - - - - rs10765995 11:12850836 C CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs1866703 11:12866800 C - ENSR00001568376 RegulatoryFeature regulatory_region_variant - - - - - - rs1866703 11:12866800 C ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs1866703 11:12866800 C ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs1866703 11:12866800 C ENSESTG00000024379 ENSESTT00000061785 Transcript intron_variant - - - - - - rs1866703 11:12866800 C 7003 NM_021961.5 Transcript intron_variant - - - - - - rs1866703 11:12866800 C CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs7936980 11:12873011 T ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs7936980 11:12873011 T ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs7936980 11:12873011 T ENSESTG00000024379 ENSESTT00000061785 Transcript intron_variant - - - - - - rs7936980 11:12873011 T 7003 NM_021961.5 Transcript intron_variant - - - - - - rs7936980 11:12873011 T CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs1371756 11:12880375 A ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs1371756 11:12880375 A ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs1371756 11:12880375 A ENSESTG00000024379 ENSESTT00000061785 Transcript intron_variant - - - - - - rs1371756 11:12880375 A 7003 NM_021961.5 Transcript intron_variant - - - - - - rs1371756 11:12880375 A CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs7130174 11:12882246 A ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs7130174 11:12882246 A ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs7130174 11:12882246 A ENSESTG00000024379 ENSESTT00000061785 Transcript intron_variant - - - - - - rs7130174 11:12882246 A 7003 NM_021961.5 Transcript intron_variant - - - - - - rs7130174 11:12882246 A CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs1866713 11:12883026 A ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs1866713 11:12883026 A ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs1866713 11:12883026 A ENSESTG00000024379 ENSESTT00000061785 Transcript intron_variant - - - - - - rs1866713 11:12883026 A 7003 NM_021961.5 Transcript intron_variant - - - - - - rs1866713 11:12883026 A CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs2403651 11:12906671 A ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs2403651 11:12906671 A ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs2403651 11:12906671 A 7003 NM_021961.5 Transcript intron_variant - - - - - - rs2403651 11:12906671 A CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs7942941 11:12911391 C ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs7942941 11:12911391 C ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs7942941 11:12911391 C 7003 NM_021961.5 Transcript intron_variant - - - - - - rs7942941 11:12911391 C CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs1440283 11:12918698 T ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs1440283 11:12918698 T ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs1440283 11:12918698 T ENSESTG00000009132 ENSESTT00000022931 Transcript upstream_gene_variant - - - - - - DISTANCE=4814 rs1440283 11:12918698 T 7003 NM_021961.5 Transcript intron_variant - - - - - - rs1440283 11:12918698 T CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs1440280 11:12929680 A ENSESTG00000024379 ENSESTT00000061760 Transcript intron_variant - - - - - - rs1440280 11:12929680 A ENSESTG00000024379 ENSESTT00000061755 Transcript intron_variant - - - - - - rs1440280 11:12929680 A ENSESTG00000009132 ENSESTT00000022931 Transcript intron_variant - - - - - - rs1440280 11:12929680 A 7003 NM_021961.5 Transcript intron_variant - - - - - - rs1440280 11:12929680 A CCDS7810.2 CCDS7810.2 Transcript intron_variant - - - - - - rs2618489 11:13998072 C ENSESTG00000018245 ENSESTT00000046025 Transcript intron_variant - - - - - - rs2618489 11:13998072 C 10418 NM_006108.3 Transcript intron_variant - - - - - - rs1919306 11:14004027 A ENSESTG00000018245 ENSESTT00000046025 Transcript intron_variant - - - - - - rs1919306 11:14004027 A 10418 NM_006108.3 Transcript intron_variant - - - - - - rs1969540 11:14061420 A ENSESTG00000018245 ENSESTT00000046025 Transcript intron_variant - - - - - - rs1969540 11:14061420 A 10418 NM_006108.3 Transcript intron_variant - - - - - - rs2915403 11:14390538 C 22800 NM_001177314.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4486 rs2915403 11:14390538 C CCDS53603.1 CCDS53603.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4599 rs1496172 11:14955907 C - - - intergenic_variant - - - - - - rs6486230 11:15296487 G - - - intergenic_variant - - - - - - rs7936491 11:15314706 T - - - intergenic_variant - - - - - - rs4388848 11:15615803 G ENSESTG00000014194 ENSESTT00000035520 Transcript intron_variant - - - - - - rs10741682 11:15704888 T - - - intergenic_variant - - - - - - rs7938924 11:15725267 G ENSESTG00000014188 ENSESTT00000035518 Transcript intron_variant - - - - - - rs974086 11:15753393 G ENSESTG00000014188 ENSESTT00000035518 Transcript intron_variant - - - - - - rs3101453 11:15930008 T - - - intergenic_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073766 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073627 Transcript intron_variant - - - - - - rs297349 11:16350457 T CCDS53605.1 CCDS53605.1 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073791 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073782 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073804 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073793 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073676 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073780 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073777 Transcript intron_variant - - - - - - rs297349 11:16350457 T 55553 NM_001145819.1 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073800 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073730 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073795 Transcript intron_variant - - - - - - rs297349 11:16350457 T 55553 NM_017508.2 Transcript intron_variant - - - - - - rs297349 11:16350457 T CCDS7821.1 CCDS7821.1 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073690 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073760 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073739 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073763 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073811 Transcript intron_variant - - - - - - rs297349 11:16350457 T 55553 NM_033326.3 Transcript intron_variant - - - - - - rs297349 11:16350457 T 55553 NM_001145811.1 Transcript intron_variant - - - - - - rs297349 11:16350457 T CCDS53604.1 CCDS53604.1 Transcript intron_variant - - - - - - rs297349 11:16350457 T ENSESTG00000029192 ENSESTT00000073737 Transcript intron_variant - - - - - - rs10832611 11:16490357 T ENSESTG00000029192 ENSESTT00000073730 Transcript intron_variant - - - - - - rs10832611 11:16490357 T ENSESTG00000029192 ENSESTT00000073627 Transcript intron_variant - - - - - - rs10832611 11:16490357 T ENSESTG00000029192 ENSESTT00000073690 Transcript intron_variant - - - - - - rs10832611 11:16490357 T ENSESTG00000029192 ENSESTT00000073739 Transcript intron_variant - - - - - - rs10832611 11:16490357 T ENSESTG00000029192 ENSESTT00000073676 Transcript intron_variant - - - - - - rs10832611 11:16490357 T 55553 NM_033326.3 Transcript intron_variant - - - - - - rs10832611 11:16490357 T ENSESTG00000029192 ENSESTT00000073719 Transcript intron_variant - - - - - - rs10832611 11:16490357 T ENSESTG00000029192 ENSESTT00000073737 Transcript intron_variant - - - - - - rs7482451 11:16679399 A ENSESTG00000029192 ENSESTT00000073676 Transcript intron_variant - - - - - - rs7482451 11:16679399 A ENSESTG00000029192 ENSESTT00000073627 Transcript intron_variant - - - - - - rs7482451 11:16679399 A ENSESTG00000029192 ENSESTT00000073719 Transcript intron_variant - - - - - - rs7482451 11:16679399 A ENSESTG00000029192 ENSESTT00000073690 Transcript intron_variant - - - - - - rs2521998 11:17333663 A ENSESTG00000016689 ENSESTT00000041983 Transcript missense_variant 426 365 122 S/N aGt/aAt - rs2521998 11:17333663 A ENSESTG00000016689 ENSESTT00000041977 Transcript missense_variant 1115 908 303 S/N aGt/aAt - PolyPhen=benign;SIFT=tolerated rs2521998 11:17333663 A CCDS41623.1 CCDS41623.1 Transcript missense_variant 908 908 303 S/N aGt/aAt - PolyPhen=benign;SIFT=tolerated rs2521998 11:17333663 A 4925 NM_005013.2 Transcript missense_variant 1153 908 303 S/N aGt/aAt - PolyPhen=benign;SIFT=tolerated rs2521998 11:17333663 A ENSESTG00000016689 ENSESTT00000041975 Transcript missense_variant 1115 908 303 S/N aGt/aAt - PolyPhen=benign;SIFT=tolerated rs10458878 11:17357013 A ENSESTG00000016689 ENSESTT00000041983 Transcript downstream_gene_variant - - - - - - DISTANCE=3149 rs10458878 11:17357013 A ENSESTG00000016689 ENSESTT00000041977 Transcript downstream_gene_variant - - - - - - DISTANCE=3149 rs10458878 11:17357013 A ENSESTG00000016736 ENSESTT00000042003 Transcript upstream_gene_variant - - - - - - DISTANCE=1987 rs10458878 11:17357013 A CCDS41623.1 CCDS41623.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4047 rs10458878 11:17357013 A ENSESTG00000017020 ENSESTT00000042730 Transcript downstream_gene_variant - - - - - - DISTANCE=2024 rs10458878 11:17357013 A 4925 NM_005013.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3943 rs10458878 11:17357013 A ENSESTG00000016689 ENSESTT00000041975 Transcript downstream_gene_variant - - - - - - DISTANCE=3149 rs6486366 11:17396128 G CCDS55748.1 CCDS55748.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2069 rs6486366 11:17396128 G 374383 NM_001202439.1 Transcript 3_prime_UTR_variant 3642 - - - - - rs12795083 11:17548737 C CCDS7825.1 CCDS7825.1 Transcript intron_variant - - - - - - rs12795083 11:17548737 C 10083 NM_153676.3 Transcript intron_variant - - - - - - rs12795083 11:17548737 C CCDS31438.1 CCDS31438.1 Transcript intron_variant - - - - - - rs12795083 11:17548737 C 10083 NM_005709.3 Transcript intron_variant - - - - - - rs1990180 11:17582470 C 340990 XM_291816.8 Transcript intron_variant - - - - - - rs1990180 11:17582470 C ENSESTG00000016771 ENSESTT00000042102 Transcript upstream_gene_variant - - - - - - DISTANCE=828 rs1990180 11:17582470 C ENSESTG00000016757 ENSESTT00000042081 Transcript downstream_gene_variant - - - - - - DISTANCE=1280 rs1990180 11:17582470 C ENSESTG00000016757 ENSESTT00000042058 Transcript downstream_gene_variant - - - - - - DISTANCE=2321 rs4756909 11:17719332 T ENSESTG00000016794 ENSESTT00000042133 Transcript downstream_gene_variant - - - - - - DISTANCE=488 rs211094 11:17987173 T ENSESTG00000007912 ENSESTT00000020024 Transcript intron_variant - - - - - - rs211094 11:17987173 T ENSESTG00000007912 ENSESTT00000020007 Transcript intron_variant - - - - - - rs211094 11:17987173 T CCDS7828.1 CCDS7828.1 Transcript intron_variant - - - - - - rs211094 11:17987173 T ENSESTG00000016834 ENSESTT00000042299 Transcript intron_variant - - - - - - rs211094 11:17987173 T ENSESTG00000007912 ENSESTT00000019986 Transcript intron_variant - - - - - - rs211094 11:17987173 T 26297 NM_012139.2 Transcript intron_variant - - - - - - rs211094 11:17987173 T ENSESTG00000007912 ENSESTT00000020021 Transcript intron_variant - - - - - - rs211094 11:17987173 T ENSESTG00000007912 ENSESTT00000020001 Transcript intron_variant - - - - - - rs211094 11:17987173 T ENSESTG00000007912 ENSESTT00000019977 Transcript intron_variant - - - - - - rs211094 11:17987173 T ENSESTG00000016834 ENSESTT00000042317 Transcript intron_variant - - - - - - rs211094 11:17987173 T ENSESTG00000007912 ENSESTT00000020004 Transcript intron_variant - - - - - - rs211101 11:18044304 T CCDS7829.1 CCDS7829.1 Transcript intron_variant - - - - - - rs211101 11:18044304 T 7166 NM_004179.2 Transcript intron_variant - - - - - - rs11024456 11:18077175 C - - - intergenic_variant - - - - - - rs7947316 11:18097387 A 113174 NM_138421.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4503 rs7947316 11:18097387 A ENSESTG00000007881 ENSESTT00000019900 Transcript intron_variant - - - - - - rs7947316 11:18097387 A CCDS31439.1 CCDS31439.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4559 rs2925154 11:18246627 G - - - intergenic_variant - - - - - - rs2658557 11:18501139 C ENSESTG00000007682 ENSESTT00000019348 Transcript downstream_gene_variant - - - - - - DISTANCE=3184 rs2658557 11:18501139 C CCDS7841.1 CCDS7841.1 Transcript downstream_gene_variant - - - - - - DISTANCE=722 rs2658557 11:18501139 C 160287 NM_001144071.1 Transcript 3_prime_UTR_variant 1982 - - - - - rs2658557 11:18501139 C ENSESTG00000007768 ENSESTT00000019691 Transcript downstream_gene_variant - - - - - - DISTANCE=771 rs2658557 11:18501139 C 160287 NM_144972.4 Transcript 3_prime_UTR_variant 2575 - - - - - rs2658557 11:18501139 C ENSESTG00000007768 ENSESTT00000019696 Transcript downstream_gene_variant - - - - - - DISTANCE=771 rs2658557 11:18501139 C CCDS7842.1 CCDS7842.1 Transcript downstream_gene_variant - - - - - - DISTANCE=954 rs2658557 11:18501139 C ENSESTG00000007768 ENSESTT00000019705 Transcript downstream_gene_variant - - - - - - DISTANCE=771 rs2658557 11:18501139 C 7251 NM_006292.3 Transcript downstream_gene_variant - - - - - - DISTANCE=719 rs4483571 11:18543100 G - ENSR00000318054 RegulatoryFeature regulatory_region_variant - - - - - - rs4483571 11:18543100 G ENSESTG00000007768 ENSESTT00000019691 Transcript intron_variant - - - - - - rs4483571 11:18543100 G ENSESTG00000007768 ENSESTT00000019696 Transcript intron_variant - - - - - - rs4483571 11:18543100 G CCDS7842.1 CCDS7842.1 Transcript intron_variant - - - - - - rs4483571 11:18543100 G 7251 NM_006292.3 Transcript intron_variant - - - - - - rs7106244 11:18823272 A - - - intergenic_variant - - - - - - rs4757720 11:18833788 G - - - intergenic_variant - - - - - - rs4543969 11:18861400 A - - - intergenic_variant - - - - - - rs1601038 11:18900228 C - - - intergenic_variant - - - - - - rs4641444 11:19135695 G ENSESTG00000019644 ENSESTT00000049317 Transcript upstream_gene_variant - - - - - - DISTANCE=3004 rs4641444 11:19135695 G 54503 NM_001001483.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2997 rs4641444 11:19135695 G CCDS44550.1 CCDS44550.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3102 rs4641444 11:19135695 G 54503 NM_019028.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2997 rs7928432 11:19333670 C - ENSR00000684971 RegulatoryFeature regulatory_region_variant - - - - - - rs7928432 11:19333670 C ENSESTG00000019773 ENSESTT00000049572 Transcript upstream_gene_variant - - - - - - DISTANCE=2538 rs1502979 11:19342948 G - ENSR00000684972 RegulatoryFeature regulatory_region_variant - - - - - - rs1502979 11:19342948 G ENSESTG00000019773 ENSESTT00000049572 Transcript intron_variant - - - - - - rs2129541 11:19627114 A CCDS53612.1 CCDS53612.1 Transcript intron_variant - - - - - - rs2129541 11:19627114 A 89797 NM_001111018.1 Transcript intron_variant - - - - - - rs10766574 11:19627494 G - ENSR00001568799 RegulatoryFeature regulatory_region_variant - - - - - - rs10766574 11:19627494 G CCDS53612.1 CCDS53612.1 Transcript intron_variant - - - - - - rs10766574 11:19627494 G 89797 NM_001111018.1 Transcript intron_variant - - - - - - rs1565044 11:19649266 T CCDS53612.1 CCDS53612.1 Transcript intron_variant - - - - - - rs1565044 11:19649266 T 89797 NM_001111018.1 Transcript intron_variant - - - - - - rs1023984 11:19649388 C CCDS53612.1 CCDS53612.1 Transcript intron_variant - - - - - - rs1023984 11:19649388 C 89797 NM_001111018.1 Transcript intron_variant - - - - - - rs7101459 11:19651261 C CCDS53612.1 CCDS53612.1 Transcript intron_variant - - - - - - rs7101459 11:19651261 C 89797 NM_001111018.1 Transcript intron_variant - - - - - - rs7935167 11:19969196 G 89797 NM_001244963.1 Transcript intron_variant - - - - - - rs7935167 11:19969196 G CCDS58126.1 CCDS58126.1 Transcript intron_variant - - - - - - rs7935167 11:19969196 G CCDS7850.1 CCDS7850.1 Transcript intron_variant - - - - - - rs7935167 11:19969196 G CCDS53612.1 CCDS53612.1 Transcript intron_variant - - - - - - rs7935167 11:19969196 G 89797 NM_001111018.1 Transcript intron_variant - - - - - - rs7935167 11:19969196 G 89797 NM_182964.5 Transcript intron_variant - - - - - - rs7935167 11:19969196 G ENSESTG00000023756 ENSESTT00000059900 Transcript intron_variant - - - - - - rs7935167 11:19969196 G CCDS7851.2 CCDS7851.2 Transcript intron_variant - - - - - - rs7935167 11:19969196 G ENSESTG00000023767 ENSESTT00000059911 Transcript upstream_gene_variant - - - - - - DISTANCE=1384 rs7935167 11:19969196 G 89797 NM_145117.4 Transcript intron_variant - - - - - - rs2584850 11:19996274 C 89797 NM_001244963.1 Transcript intron_variant - - - - - - rs2584850 11:19996274 C CCDS58126.1 CCDS58126.1 Transcript intron_variant - - - - - - rs2584850 11:19996274 C CCDS7850.1 CCDS7850.1 Transcript intron_variant - - - - - - rs2584850 11:19996274 C CCDS53612.1 CCDS53612.1 Transcript intron_variant - - - - - - rs2584850 11:19996274 C 89797 NM_001111018.1 Transcript intron_variant - - - - - - rs2584850 11:19996274 C 89797 NM_182964.5 Transcript intron_variant - - - - - - rs2584850 11:19996274 C ENSESTG00000024552 ENSESTT00000062050 Transcript downstream_gene_variant - - - - - - DISTANCE=4109 rs2584850 11:19996274 C CCDS7851.2 CCDS7851.2 Transcript intron_variant - - - - - - rs2584850 11:19996274 C ENSESTG00000023767 ENSESTT00000059911 Transcript intron_variant - - - - - - rs2584850 11:19996274 C 89797 NM_145117.4 Transcript intron_variant - - - - - - rs2625299 11:20034285 C 89797 NM_001244963.1 Transcript intron_variant - - - - - - rs2625299 11:20034285 C CCDS58126.1 CCDS58126.1 Transcript intron_variant - - - - - - rs2625299 11:20034285 C CCDS7850.1 CCDS7850.1 Transcript intron_variant - - - - - - rs2625299 11:20034285 C CCDS53612.1 CCDS53612.1 Transcript intron_variant - - - - - - rs2625299 11:20034285 C 89797 NM_001111018.1 Transcript intron_variant - - - - - - rs2625299 11:20034285 C 89797 NM_182964.5 Transcript intron_variant - - - - - - rs2625299 11:20034285 C ENSESTG00000024547 ENSESTT00000062029 Transcript intron_variant - - - - - - rs2625299 11:20034285 C ENSESTG00000023776 ENSESTT00000059954 Transcript intron_variant - - - - - - rs2625299 11:20034285 C CCDS7851.2 CCDS7851.2 Transcript intron_variant - - - - - - rs2625299 11:20034285 C 89797 NM_145117.4 Transcript intron_variant - - - - - - rs7121946 11:20513069 G ENSESTG00000024461 ENSESTT00000061851 Transcript intron_variant - - - - - - rs7121946 11:20513069 G ENSESTG00000024220 ENSESTT00000061510 Transcript intron_variant - - - - - - rs7121946 11:20513069 G 10196 NM_001145166.1 Transcript intron_variant - - - - - - rs7121946 11:20513069 G 10196 NM_001145167.1 Transcript intron_variant - - - - - - rs7121946 11:20513069 G CCDS7853.1 CCDS7853.1 Transcript intron_variant - - - - - - rs7121946 11:20513069 G CCDS44554.1 CCDS44554.1 Transcript intron_variant - - - - - - rs7121946 11:20513069 G ENSESTG00000024474 ENSESTT00000061865 Transcript upstream_gene_variant - - - - - - DISTANCE=4865 rs7121946 11:20513069 G ENSESTG00000024220 ENSESTT00000061447 Transcript intron_variant - - - - - - rs7121946 11:20513069 G 10196 NM_005788.3 Transcript intron_variant - - - - - - rs6483697 11:20515555 A ENSESTG00000024461 ENSESTT00000061851 Transcript intron_variant - - - - - - rs6483697 11:20515555 A ENSESTG00000024220 ENSESTT00000061510 Transcript intron_variant - - - - - - rs6483697 11:20515555 A 10196 NM_001145166.1 Transcript intron_variant - - - - - - rs6483697 11:20515555 A 10196 NM_001145167.1 Transcript intron_variant - - - - - - rs6483697 11:20515555 A CCDS7853.1 CCDS7853.1 Transcript intron_variant - - - - - - rs6483697 11:20515555 A CCDS44554.1 CCDS44554.1 Transcript intron_variant - - - - - - rs6483697 11:20515555 A ENSESTG00000024220 ENSESTT00000061447 Transcript intron_variant - - - - - - rs6483697 11:20515555 A 10196 NM_005788.3 Transcript intron_variant - - - - - - rs1792967 11:20686284 C 4745 NM_201551.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4833 rs1792967 11:20686284 C ENSESTG00000024367 ENSESTT00000061744 Transcript upstream_gene_variant - - - - - - DISTANCE=4833 rs1792967 11:20686284 C ENSESTG00000024443 ENSESTT00000061835 Transcript downstream_gene_variant - - - - - - DISTANCE=3702 rs1792967 11:20686284 C ENSESTG00000024367 ENSESTT00000061752 Transcript upstream_gene_variant - - - - - - DISTANCE=4833 rs1792967 11:20686284 C 4745 NM_006157.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4833 rs1792967 11:20686284 C CCDS44555.1 CCDS44555.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4986 rs1792967 11:20686284 C CCDS7855.1 CCDS7855.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4986 rs1792967 11:20686284 C ENSESTG00000024367 ENSESTT00000061769 Transcript upstream_gene_variant - - - - - - DISTANCE=4833 rs1792988 11:20719119 A 4745 NM_006157.3 Transcript intron_variant - - - - - - rs1792988 11:20719119 A CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs1792988 11:20719119 A 4745 NM_201551.1 Transcript intron_variant - - - - - - rs1792988 11:20719119 A ENSESTG00000024367 ENSESTT00000061744 Transcript intron_variant - - - - - - rs1792988 11:20719119 A CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs1792988 11:20719119 A ENSESTG00000024367 ENSESTT00000061769 Transcript intron_variant - - - - - - rs1792988 11:20719119 A ENSESTG00000024367 ENSESTT00000061752 Transcript intron_variant - - - - - - rs443495 11:20844338 A ENSESTG00000024367 ENSESTT00000061782 Transcript intron_variant - - - - - - rs443495 11:20844338 A 4745 NM_201551.1 Transcript intron_variant - - - - - - rs443495 11:20844338 A ENSESTG00000024367 ENSESTT00000061744 Transcript intron_variant - - - - - - rs443495 11:20844338 A ENSESTG00000024367 ENSESTT00000061790 Transcript intron_variant - - - - - - rs443495 11:20844338 A ENSESTG00000024367 ENSESTT00000061752 Transcript intron_variant - - - - - - rs443495 11:20844338 A 4745 NM_006157.3 Transcript intron_variant - - - - - - rs443495 11:20844338 A CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs443495 11:20844338 A CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs443495 11:20844338 A ENSESTG00000024367 ENSESTT00000061769 Transcript intron_variant - - - - - - rs919475 11:20862546 T ENSESTG00000024367 ENSESTT00000061782 Transcript intron_variant - - - - - - rs919475 11:20862546 T 4745 NM_201551.1 Transcript intron_variant - - - - - - rs919475 11:20862546 T ENSESTG00000024367 ENSESTT00000061744 Transcript intron_variant - - - - - - rs919475 11:20862546 T ENSESTG00000024367 ENSESTT00000061790 Transcript intron_variant - - - - - - rs919475 11:20862546 T ENSESTG00000024367 ENSESTT00000061752 Transcript intron_variant - - - - - - rs919475 11:20862546 T 4745 NM_006157.3 Transcript intron_variant - - - - - - rs919475 11:20862546 T CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs919475 11:20862546 T CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs919475 11:20862546 T ENSESTG00000024367 ENSESTT00000061769 Transcript intron_variant - - - - - - rs7482426 11:20902580 G 4745 NM_201551.1 Transcript intron_variant - - - - - - rs7482426 11:20902580 G ENSESTG00000024367 ENSESTT00000061744 Transcript intron_variant - - - - - - rs7482426 11:20902580 G ENSESTG00000024367 ENSESTT00000061790 Transcript intron_variant - - - - - - rs7482426 11:20902580 G ENSESTG00000024367 ENSESTT00000061752 Transcript intron_variant - - - - - - rs7482426 11:20902580 G 4745 NM_006157.3 Transcript intron_variant - - - - - - rs7482426 11:20902580 G CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs7482426 11:20902580 G CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs7482426 11:20902580 G ENSESTG00000024367 ENSESTT00000061769 Transcript intron_variant - - - - - - rs1914252 11:21034842 C ENSESTG00000016654 ENSESTT00000041813 Transcript intron_variant - - - - - - rs1914252 11:21034842 C 4745 NM_006157.3 Transcript intron_variant - - - - - - rs1914252 11:21034842 C ENSESTG00000016654 ENSESTT00000041793 Transcript intron_variant - - - - - - rs1914252 11:21034842 C CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs1914252 11:21034842 C 4745 NM_201551.1 Transcript intron_variant - - - - - - rs1914252 11:21034842 C CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs1356295 11:21043945 C ENSESTG00000016654 ENSESTT00000041813 Transcript intron_variant - - - - - - rs1356295 11:21043945 C 4745 NM_006157.3 Transcript intron_variant - - - - - - rs1356295 11:21043945 C ENSESTG00000016654 ENSESTT00000041793 Transcript intron_variant - - - - - - rs1356295 11:21043945 C CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs1356295 11:21043945 C 4745 NM_201551.1 Transcript intron_variant - - - - - - rs1356295 11:21043945 C CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs7945892 11:21093539 G ENSESTG00000016654 ENSESTT00000041813 Transcript intron_variant - - - - - - rs7945892 11:21093539 G 4745 NM_006157.3 Transcript intron_variant - - - - - - rs7945892 11:21093539 G ENSESTG00000016654 ENSESTT00000041793 Transcript intron_variant - - - - - - rs7945892 11:21093539 G CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs7945892 11:21093539 G 4745 NM_201551.1 Transcript intron_variant - - - - - - rs7945892 11:21093539 G CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs1791815 11:21196731 A ENSESTG00000016654 ENSESTT00000041813 Transcript intron_variant - - - - - - rs1791815 11:21196731 A 4745 NM_006157.3 Transcript intron_variant - - - - - - rs1791815 11:21196731 A ENSESTG00000016654 ENSESTT00000041793 Transcript intron_variant - - - - - - rs1791815 11:21196731 A CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs1791815 11:21196731 A 4745 NM_201551.1 Transcript intron_variant - - - - - - rs1791815 11:21196731 A CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs4356225 11:21352920 A ENSESTG00000016654 ENSESTT00000041813 Transcript intron_variant - - - - - - rs4356225 11:21352920 A 4745 NM_006157.3 Transcript intron_variant - - - - - - rs4356225 11:21352920 A ENSESTG00000016654 ENSESTT00000041793 Transcript intron_variant - - - - - - rs4356225 11:21352920 A CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs4356225 11:21352920 A 4745 NM_201551.1 Transcript intron_variant - - - - - - rs4356225 11:21352920 A CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs4356225 11:21352920 A ENSESTG00000016654 ENSESTT00000041822 Transcript intron_variant - - - - - - rs6483766 11:21368489 C ENSESTG00000016654 ENSESTT00000041813 Transcript intron_variant - - - - - - rs6483766 11:21368489 C 4745 NM_006157.3 Transcript intron_variant - - - - - - rs6483766 11:21368489 C ENSESTG00000016654 ENSESTT00000041793 Transcript intron_variant - - - - - - rs6483766 11:21368489 C CCDS44555.1 CCDS44555.1 Transcript intron_variant - - - - - - rs6483766 11:21368489 C 4745 NM_201551.1 Transcript intron_variant - - - - - - rs6483766 11:21368489 C CCDS7855.1 CCDS7855.1 Transcript intron_variant - - - - - - rs6483766 11:21368489 C ENSESTG00000016654 ENSESTT00000041822 Transcript intron_variant - - - - - - rs7938581 11:21658560 T - - - intergenic_variant - - - - - - rs10766846 11:21681961 T - - - intergenic_variant - - - - - - rs4556540 11:21701144 G - - - intergenic_variant - - - - - - rs10741937 11:22351482 T ENSESTG00000031231 ENSESTT00000078697 Transcript intron_variant - - - - - - rs4334011 11:22466896 C ENSESTG00000031180 ENSESTT00000078550 Transcript downstream_gene_variant - - - - - - DISTANCE=341 rs10766952 11:22563362 C - - - intergenic_variant - - - - - - rs441141 11:22730585 G CCDS7858.1 CCDS7858.1 Transcript intron_variant - - - - - - rs441141 11:22730585 G ENSESTG00000031112 ENSESTT00000078361 Transcript intron_variant - - - - - - rs441141 11:22730585 G ENSESTG00000031112 ENSESTT00000078392 Transcript intron_variant - - - - - - rs441141 11:22730585 G ENSESTG00000031112 ENSESTT00000078427 Transcript intron_variant - - - - - - rs441141 11:22730585 G ENSESTG00000031112 ENSESTT00000078419 Transcript intron_variant - - - - - - rs441141 11:22730585 G 2620 NM_001143830.1 Transcript intron_variant - - - - - - rs441141 11:22730585 G ENSESTG00000031112 ENSESTT00000078406 Transcript intron_variant - - - - - - rs441141 11:22730585 G 2620 NM_177553.2 Transcript intron_variant - - - - - - rs441141 11:22730585 G ENSESTG00000031112 ENSESTT00000078442 Transcript intron_variant - - - - - - rs441141 11:22730585 G ENSESTG00000031112 ENSESTT00000078457 Transcript intron_variant - - - - - - rs441141 11:22730585 G ENSESTG00000031170 ENSESTT00000078503 Transcript downstream_gene_variant - - - - - - DISTANCE=1370 rs441141 11:22730585 G 2620 NM_005256.3 Transcript intron_variant - - - - - - rs2433523 11:23013507 T - - - intergenic_variant - - - - - - rs2468641 11:23183933 A - - - intergenic_variant - - - - - - rs1482733 11:23243962 T - - - intergenic_variant - - - - - - rs4923079 11:23256307 T - - - intergenic_variant - - - - - - rs6483910 11:23273703 C - - - intergenic_variant - - - - - - rs4301787 11:23305260 C - - - intergenic_variant - - - - - - rs4923093 11:23366361 C - - - intergenic_variant - - - - - - rs1118830 11:23513176 A - - - intergenic_variant - - - - - - rs4354689 11:23677721 A - - - intergenic_variant - - - - - - rs6483987 11:23810855 C - - - intergenic_variant - - - - - - rs4326796 11:23828520 A - - - intergenic_variant - - - - - - rs2955459 11:24035263 C - - - intergenic_variant - - - - - - rs2947725 11:24148898 T - - - intergenic_variant - - - - - - rs10734349 11:24203350 T - - - intergenic_variant - - - - - - rs10742032 11:24217588 T - - - intergenic_variant - - - - - - rs7926095 11:24348079 A - - - intergenic_variant - - - - - - rs1899544 11:24393569 T - - - intergenic_variant - - - - - - rs2403914 11:24411780 A - ENSR00000559939 RegulatoryFeature regulatory_region_variant - - - - - - rs2403914 11:24411780 A - - - intergenic_variant - - - - - - rs2403923 11:24424367 T - - - intergenic_variant - - - - - - rs4923174 11:24451782 A - - - intergenic_variant - - - - - - rs1509585 11:24535613 T - ENSR00001569004 RegulatoryFeature regulatory_region_variant - - - - - - rs1509585 11:24535613 T CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs1509585 11:24535613 T 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs1509585 11:24535613 T 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs1509585 11:24535613 T 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs1396851 11:24553240 T CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs1396851 11:24553240 T 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs1396851 11:24553240 T 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs1396851 11:24553240 T 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs2403973 11:24660543 T CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs2403973 11:24660543 T 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs2403973 11:24660543 T 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs2403973 11:24660543 T 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs2403969 11:24666142 C CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs2403969 11:24666142 C 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs2403969 11:24666142 C 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs2403969 11:24666142 C 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs2631516 11:24815969 T CCDS58128.1 CCDS58128.1 Transcript intron_variant - - - - - - rs2631516 11:24815969 T CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs2631516 11:24815969 T 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs2631516 11:24815969 T 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs2631516 11:24815969 T 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs2716546 11:24816013 G CCDS58128.1 CCDS58128.1 Transcript intron_variant - - - - - - rs2716546 11:24816013 G CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs2716546 11:24816013 G 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs2716546 11:24816013 G 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs2716546 11:24816013 G 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs1386243 11:24825389 G CCDS58128.1 CCDS58128.1 Transcript intron_variant - - - - - - rs1386243 11:24825389 G CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs1386243 11:24825389 G 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs1386243 11:24825389 G 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs1386243 11:24825389 G 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs1486691 11:24827237 A CCDS58128.1 CCDS58128.1 Transcript intron_variant - - - - - - rs1486691 11:24827237 A CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs1486691 11:24827237 A 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs1486691 11:24827237 A 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs1486691 11:24827237 A 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs1486690 11:24827638 A CCDS58128.1 CCDS58128.1 Transcript intron_variant - - - - - - rs1486690 11:24827638 A CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs1486690 11:24827638 A 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs1486690 11:24827638 A 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs1486690 11:24827638 A 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs1960471 11:24884687 A CCDS58128.1 CCDS58128.1 Transcript intron_variant - - - - - - rs1960471 11:24884687 A CCDS31446.1 CCDS31446.1 Transcript intron_variant - - - - - - rs1960471 11:24884687 A 338645 NM_001252008.1 Transcript intron_variant - - - - - - rs1960471 11:24884687 A 338645 NM_001009909.3 Transcript intron_variant - - - - - - rs1960471 11:24884687 A 338645 NM_001252010.1 Transcript intron_variant - - - - - - rs7931714 11:25184714 T - - - intergenic_variant - - - - - - rs10742073 11:25202479 T - - - intergenic_variant - - - - - - rs1582731 11:25229014 T - - - intergenic_variant - - - - - - rs10834629 11:25259147 G - - - intergenic_variant - - - - - - rs6484123 11:25262407 A - - - intergenic_variant - - - - - - rs1477566 11:25263254 C - - - intergenic_variant - - - - - - rs1582729 11:25323707 A - - - intergenic_variant - - - - - - rs3910758 11:25526374 G - - - intergenic_variant - - - - - - rs7358410 11:25675720 A - - - intergenic_variant - - - - - - rs6484158 11:25675963 A - - - intergenic_variant - - - - - - rs4244520 11:25790575 A - - - intergenic_variant - - - - - - rs3108824 11:26274772 A ENSESTG00000008859 ENSESTT00000022232 Transcript intron_variant - - - - - - rs6484198 11:26294883 C ENSESTG00000008859 ENSESTT00000022232 Transcript intron_variant - - - - - - rs1841570 11:26420813 C ENSESTG00000008859 ENSESTT00000022232 Transcript intron_variant - - - - - - rs1841570 11:26420813 C CCDS31447.1 CCDS31447.1 Transcript intron_variant - - - - - - rs1841570 11:26420813 C ENSESTG00000008859 ENSESTT00000022240 Transcript intron_variant - - - - - - rs1841570 11:26420813 C 63982 NM_031418.2 Transcript intron_variant - - - - - - rs1841570 11:26420813 C ENSESTG00000008859 ENSESTT00000022237 Transcript intron_variant - - - - - - rs4619106 11:26755926 G - - - intergenic_variant - - - - - - rs1597438 11:26898283 A - - - intergenic_variant - - - - - - rs10742163 11:26903983 G - - - intergenic_variant - - - - - - rs10767586 11:26918649 T - ENSR00001569058 RegulatoryFeature regulatory_region_variant - - - - - - rs10767586 11:26918649 T - - - intergenic_variant - - - - - - rs1020373 11:27024166 G - - - intergenic_variant - - - - - - rs983405 11:27036715 A - - - intergenic_variant - - - - - - rs1445321 11:27039929 A - - - intergenic_variant - - - - - - rs1596714 11:27049370 T - - - intergenic_variant - - - - - - rs7131593 11:27055490 C - - - intergenic_variant - - - - - - rs10767598 11:27077118 T CCDS7862.1 CCDS7862.1 Transcript synonymous_variant 141 141 47 S tcC/tcT - rs10767598 11:27077118 T ENSESTG00000025261 ENSESTT00000063978 Transcript synonymous_variant 533 141 47 S tcC/tcT - rs10767598 11:27077118 T ENSESTG00000025261 ENSESTT00000063946 Transcript synonymous_variant 635 141 47 S tcC/tcT - rs10767598 11:27077118 T 8424 NM_003986.2 Transcript synonymous_variant 509 141 47 S tcC/tcT - rs2083746 11:27097378 C CCDS7862.1 CCDS7862.1 Transcript intron_variant - - - - - - rs2083746 11:27097378 C ENSESTG00000025261 ENSESTT00000063978 Transcript intron_variant - - - - - - rs2083746 11:27097378 C ENSESTG00000025261 ENSESTT00000063946 Transcript intron_variant - - - - - - rs2083746 11:27097378 C 8424 NM_003986.2 Transcript intron_variant - - - - - - rs1900063 11:27099943 C CCDS7862.1 CCDS7862.1 Transcript intron_variant - - - - - - rs1900063 11:27099943 C ENSESTG00000025261 ENSESTT00000063978 Transcript intron_variant - - - - - - rs1900063 11:27099943 C ENSESTG00000025261 ENSESTT00000063946 Transcript intron_variant - - - - - - rs1900063 11:27099943 C 8424 NM_003986.2 Transcript intron_variant - - - - - - rs969853 11:27104415 G CCDS7862.1 CCDS7862.1 Transcript intron_variant - - - - - - rs969853 11:27104415 G ENSESTG00000025261 ENSESTT00000063978 Transcript intron_variant - - - - - - rs969853 11:27104415 G ENSESTG00000025261 ENSESTT00000063946 Transcript intron_variant - - - - - - rs969853 11:27104415 G 8424 NM_003986.2 Transcript intron_variant - - - - - - rs1156471 11:27119092 A CCDS7862.1 CCDS7862.1 Transcript intron_variant - - - - - - rs1156471 11:27119092 A ENSESTG00000025261 ENSESTT00000063978 Transcript intron_variant - - - - - - rs1156471 11:27119092 A ENSESTG00000025261 ENSESTT00000063946 Transcript intron_variant - - - - - - rs1156471 11:27119092 A 8424 NM_003986.2 Transcript intron_variant - - - - - - rs1155086 11:27125532 A CCDS7862.1 CCDS7862.1 Transcript intron_variant - - - - - - rs1155086 11:27125532 A ENSESTG00000025261 ENSESTT00000063978 Transcript intron_variant - - - - - - rs1155086 11:27125532 A ENSESTG00000025261 ENSESTT00000063946 Transcript intron_variant - - - - - - rs1155086 11:27125532 A 8424 NM_003986.2 Transcript intron_variant - - - - - - rs7939156 11:27138725 G CCDS7862.1 CCDS7862.1 Transcript intron_variant - - - - - - rs7939156 11:27138725 G ENSESTG00000025261 ENSESTT00000063978 Transcript intron_variant - - - - - - rs7939156 11:27138725 G ENSESTG00000025261 ENSESTT00000063946 Transcript intron_variant - - - - - - rs7939156 11:27138725 G 8424 NM_003986.2 Transcript intron_variant - - - - - - rs1025879 11:27150148 G CCDS7862.1 CCDS7862.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1148 rs1025879 11:27150148 G ENSESTG00000025261 ENSESTT00000063978 Transcript downstream_gene_variant - - - - - - DISTANCE=925 rs1025879 11:27150148 G ENSESTG00000025261 ENSESTT00000063946 Transcript downstream_gene_variant - - - - - - DISTANCE=925 rs1025879 11:27150148 G 8424 NM_003986.2 Transcript downstream_gene_variant - - - - - - DISTANCE=794 rs1965824 11:27151992 C CCDS7862.1 CCDS7862.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2992 rs1965824 11:27151992 C ENSESTG00000025261 ENSESTT00000063978 Transcript downstream_gene_variant - - - - - - DISTANCE=2769 rs1965824 11:27151992 C ENSESTG00000025261 ENSESTT00000063946 Transcript downstream_gene_variant - - - - - - DISTANCE=2769 rs1965824 11:27151992 C 8424 NM_003986.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2638 rs1813092 11:27153776 G CCDS7862.1 CCDS7862.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4776 rs1813092 11:27153776 G ENSESTG00000025261 ENSESTT00000063978 Transcript downstream_gene_variant - - - - - - DISTANCE=4553 rs1813092 11:27153776 G ENSESTG00000025261 ENSESTT00000063946 Transcript downstream_gene_variant - - - - - - DISTANCE=4553 rs1813092 11:27153776 G 8424 NM_003986.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4422 rs1020273 11:27169654 G - - - intergenic_variant - - - - - - rs1838011 11:27180700 C - ENSR00001569093 RegulatoryFeature regulatory_region_variant - - - - - - rs1838011 11:27180700 C - - - intergenic_variant - - - - - - rs2010741 11:27211433 G - - - intergenic_variant - - - - - - rs1822334 11:27213528 T - - - intergenic_variant - - - - - - rs11030089 11:27648390 A - ENSR00001569169 RegulatoryFeature regulatory_region_variant - - - - - - rs11030089 11:27648390 A ENSESTG00000025386 ENSESTT00000064057 Transcript intron_variant - - - - - - rs11030089 11:27648390 A 497258 NR_033313.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11030089 11:27648390 A 497258 NR_033312.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11030089 11:27648390 A 497258 NR_033314.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11030089 11:27648390 A 497258 NR_002832.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs11030089 11:27648390 A 497258 NR_033315.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10767661 11:27695436 G - ENSR00000560209 RegulatoryFeature regulatory_region_variant - - - - - - rs10767661 11:27695436 G ENSESTG00000025415 ENSESTT00000064146 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143807.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_170733.3 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143809.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G ENSESTG00000025415 ENSESTT00000064102 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_170731.4 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 497258 NR_033314.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10767661 11:27695436 G ENSESTG00000025415 ENSESTT00000064168 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143811.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G CCDS44558.1 CCDS44558.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G ENSESTG00000025415 ENSESTT00000064129 Transcript intron_variant - - - - - - rs10767661 11:27695436 G CCDS7865.1 CCDS7865.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143805.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 497258 NR_033313.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10767661 11:27695436 G 497258 NR_033312.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10767661 11:27695436 G 497258 NR_002832.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143814.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G ENSESTG00000025386 ENSESTT00000064057 Transcript intron_variant - - - - - - rs10767661 11:27695436 G ENSESTG00000025386 ENSESTT00000064082 Transcript upstream_gene_variant - - - - - - DISTANCE=2109 rs10767661 11:27695436 G 627 NM_170734.3 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143812.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143810.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143808.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_170732.4 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 497258 NR_033315.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10767661 11:27695436 G 627 NM_001709.4 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143813.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G 627 NM_001143806.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G CCDS41628.1 CCDS41628.1 Transcript intron_variant - - - - - - rs10767661 11:27695436 G ENSESTG00000025415 ENSESTT00000064112 Transcript intron_variant - - - - - - rs2956845 11:27958708 G - - - intergenic_variant - - - - - - rs1525706 11:27972751 G - - - intergenic_variant - - - - - - rs2170791 11:28225459 A CCDS44559.1 CCDS44559.1 Transcript intron_variant - - - - - - rs2170791 11:28225459 A 196074 NM_152636.2 Transcript intron_variant - - - - - - rs2170791 11:28225459 A 196074 NM_001113528.1 Transcript intron_variant - - - - - - rs2170791 11:28225459 A CCDS31450.1 CCDS31450.1 Transcript intron_variant - - - - - - rs959529 11:28249009 T CCDS44559.1 CCDS44559.1 Transcript intron_variant - - - - - - rs959529 11:28249009 T 196074 NM_152636.2 Transcript intron_variant - - - - - - rs959529 11:28249009 T 196074 NM_001113528.1 Transcript intron_variant - - - - - - rs959529 11:28249009 T CCDS31450.1 CCDS31450.1 Transcript intron_variant - - - - - - rs4582963 11:28485366 A - ENSR00000560304 RegulatoryFeature regulatory_region_variant - - - - - - rs4582963 11:28485366 A - - - intergenic_variant - - - - - - rs7928847 11:28554710 C - - - intergenic_variant - - - - - - rs10767728 11:28632702 T - - - intergenic_variant - - - - - - rs532435 11:28803164 C - - - intergenic_variant - - - - - - rs2945092 11:28845178 C - - - intergenic_variant - - - - - - rs4923589 11:29039162 A - - - intergenic_variant - - - - - - rs4382888 11:29052153 A - - - intergenic_variant - - - - - - rs7933302 11:29085431 T - ENSR00001052144 RegulatoryFeature regulatory_region_variant - - - - - - rs7933302 11:29085431 T - - - intergenic_variant - - - - - - rs6484424 11:29122168 G - - - intergenic_variant - - - - - - rs4544032 11:29296600 G - - - intergenic_variant - - - - - - rs7105126 11:29306926 G - - - intergenic_variant - - - - - - rs6484441 11:29322543 C - ENSR00001569279 RegulatoryFeature regulatory_region_variant - - - - - - rs6484441 11:29322543 C - - - intergenic_variant - - - - - - rs4923604 11:29327560 A - ENSR00001569280 RegulatoryFeature regulatory_region_variant - - - - - - rs4923604 11:29327560 A - - - intergenic_variant - - - - - - rs7932580 11:29398636 C ENSESTG00000009263 ENSESTT00000023216 Transcript intron_variant - - - - - - rs7947662 11:29398797 C ENSESTG00000009263 ENSESTT00000023216 Transcript intron_variant - - - - - - rs7481155 11:29420665 G ENSESTG00000009263 ENSESTT00000023216 Transcript intron_variant - - - - - - rs4923608 11:29464507 T ENSESTG00000009263 ENSESTT00000023216 Transcript intron_variant - - - - - - rs433606 11:29782117 A - - - intergenic_variant - - - - - - rs594712 11:30047518 C - ENSR00000560454 RegulatoryFeature regulatory_region_variant - - - - - - rs594712 11:30047518 C - - - intergenic_variant - - - - - - rs990167 11:30139452 T - - - intergenic_variant - - - - - - rs649663 11:30145554 G - - - intergenic_variant - - - - - - rs628032 11:30145737 G - - - intergenic_variant - - - - - - rs1222206 11:30358475 T ENSESTG00000000062 ENSESTT00000000158 Transcript downstream_gene_variant - - - - - - DISTANCE=66 rs1222206 11:30358475 T CCDS7869.1 CCDS7869.1 Transcript downstream_gene_variant - - - - - - DISTANCE=133 rs1222206 11:30358475 T 120534 NM_152316.1 Transcript 3_prime_UTR_variant 1080 - - - - - rs1222206 11:30358475 T ENSESTG00000000062 ENSESTT00000000159 Transcript downstream_gene_variant - - - - - - DISTANCE=122 rs808398 11:30676031 T - - - intergenic_variant - - - - - - rs1232033 11:30828105 T ENSESTG00000019141 ENSESTT00000048123 Transcript intron_variant - - - - - - rs290103 11:31014865 G 100506627 NM_020869.3 Transcript upstream_gene_variant - - - - - - DISTANCE=632 rs6484505 11:31463005 T 196294 NM_144981.1 Transcript intron_variant - - - - - - rs6484505 11:31463005 T ENSESTG00000019300 ENSESTT00000048506 Transcript intron_variant - - - - - - rs6484505 11:31463005 T CCDS7874.1 CCDS7874.1 Transcript intron_variant - - - - - - rs7937261 11:31628004 A ENSESTG00000019214 ENSESTT00000048384 Transcript intron_variant - - - - - - rs7937261 11:31628004 A CCDS7875.2 CCDS7875.2 Transcript intron_variant - - - - - - rs7937261 11:31628004 A 26610 NM_019040.3 Transcript intron_variant - - - - - - rs223062 11:32123510 T CCDS7876.1 CCDS7876.1 Transcript intron_variant - - - - - - rs223062 11:32123510 T ENSESTG00000025732 ENSESTT00000064961 Transcript intron_variant - - - - - - rs223062 11:32123510 T ENSESTG00000025732 ENSESTT00000064995 Transcript intron_variant - - - - - - rs223062 11:32123510 T 5954 NM_002901.2 Transcript intron_variant - - - - - - rs271027 11:32728518 T - ENSR00001569414 RegulatoryFeature regulatory_region_variant - - - - - - rs271027 11:32728518 T ENSESTG00000025886 ENSESTT00000065313 Transcript intron_variant - - - - - - rs271027 11:32728518 T CCDS41630.1 CCDS41630.1 Transcript intron_variant - - - - - - rs271027 11:32728518 T 493860 NM_001008391.2 Transcript intron_variant - - - - - - rs156160 11:32773569 C ENSESTG00000025886 ENSESTT00000065313 Transcript intron_variant - - - - - - rs156160 11:32773569 C CCDS41630.1 CCDS41630.1 Transcript intron_variant - - - - - - rs156160 11:32773569 C 493860 NM_001008391.2 Transcript intron_variant - - - - - - rs156160 11:32773569 C ENSESTG00000025886 ENSESTT00000065330 Transcript intron_variant - - - - - - rs266491 11:33350325 T CCDS41634.1 CCDS41634.1 Transcript intron_variant - - - - - - rs266491 11:33350325 T 10114 NM_005734.3 Transcript intron_variant - - - - - - rs266491 11:33350325 T 10114 NM_001048200.1 Transcript intron_variant - - - - - - rs266491 11:33350325 T ENSESTG00000029523 ENSESTT00000074474 Transcript intron_variant - - - - - - rs266491 11:33350325 T CCDS7884.1 CCDS7884.1 Transcript intron_variant - - - - - - rs266491 11:33350325 T ENSESTG00000029523 ENSESTT00000074468 Transcript intron_variant - - - - - - rs831634 11:33740109 C - ENSR00001569495 RegulatoryFeature regulatory_region_variant - - - - - - rs831634 11:33740109 C ENSESTG00000029709 ENSESTT00000074843 Transcript intron_variant - - - - - - rs831634 11:33740109 C CCDS7886.1 CCDS7886.1 Transcript intron_variant - - - - - - rs831634 11:33740109 C 966 NM_000611.5 Transcript intron_variant - - - - - - rs831634 11:33740109 C 966 NM_203331.2 Transcript intron_variant - - - - - - rs831634 11:33740109 C 966 NM_001127223.1 Transcript intron_variant - - - - - - rs831634 11:33740109 C 966 NM_203330.2 Transcript intron_variant - - - - - - rs831634 11:33740109 C 966 NM_001127227.1 Transcript intron_variant - - - - - - rs831634 11:33740109 C 966 NM_203329.2 Transcript intron_variant - - - - - - rs831634 11:33740109 C 966 NM_001127226.1 Transcript intron_variant - - - - - - rs831634 11:33740109 C 966 NM_001127225.1 Transcript intron_variant - - - - - - rs831634 11:33740109 C ENSESTG00000029709 ENSESTT00000074825 Transcript intron_variant - - - - - - rs4756103 11:34096330 G CCDS31454.1 CCDS31454.1 Transcript intron_variant - - - - - - rs4756103 11:34096330 G 4076 NM_005898.4 Transcript intron_variant - - - - - - rs4756103 11:34096330 G 4076 NM_203364.2 Transcript intron_variant - - - - - - rs4756103 11:34096330 G CCDS31453.1 CCDS31453.1 Transcript intron_variant - - - - - - rs4756103 11:34096330 G ENSESTG00000008121 ENSESTT00000020557 Transcript downstream_gene_variant - - - - - - DISTANCE=2802 rs4756103 11:34096330 G ENSESTG00000008121 ENSESTT00000020560 Transcript downstream_gene_variant - - - - - - DISTANCE=2843 rs2957488 11:34116949 T CCDS31454.1 CCDS31454.1 Transcript intron_variant - - - - - - rs2957488 11:34116949 T ENSESTG00000008147 ENSESTT00000020632 Transcript upstream_gene_variant - - - - - - DISTANCE=1864 rs2957488 11:34116949 T 4076 NM_005898.4 Transcript intron_variant - - - - - - rs2957488 11:34116949 T 4076 NM_203364.2 Transcript intron_variant - - - - - - rs2957488 11:34116949 T ENSESTG00000008147 ENSESTT00000020626 Transcript upstream_gene_variant - - - - - - DISTANCE=417 rs2957488 11:34116949 T CCDS31453.1 CCDS31453.1 Transcript intron_variant - - - - - - rs2982590 11:34122369 T CCDS31454.1 CCDS31454.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3041 rs2982590 11:34122369 T ENSESTG00000008147 ENSESTT00000020632 Transcript downstream_gene_variant - - - - - - DISTANCE=1166 rs2982590 11:34122369 T 4076 NM_203364.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1762 rs2982590 11:34122369 T ENSESTG00000008147 ENSESTT00000020626 Transcript downstream_gene_variant - - - - - - DISTANCE=141 rs2982590 11:34122369 T 55226 NM_001144030.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4742 rs2982590 11:34122369 T ENSESTG00000008177 ENSESTT00000020709 Transcript upstream_gene_variant - - - - - - DISTANCE=4780 rs2982590 11:34122369 T 55226 NM_024662.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4742 rs2982590 11:34122369 T 4076 NM_005898.4 Transcript 3_prime_UTR_variant 3774 - - - - - rs2982590 11:34122369 T CCDS31453.1 CCDS31453.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1455 rs2982589 11:34127400 C - ENSR00001569512 RegulatoryFeature regulatory_region_variant - - - - - - rs2982589 11:34127400 C 55226 NM_024662.2 Transcript intron_variant - - - - - - rs2982589 11:34127400 C ENSESTG00000008177 ENSESTT00000020718 Transcript upstream_gene_variant - - - - - - DISTANCE=180 rs2982589 11:34127400 C CCDS7889.1 CCDS7889.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2373 rs2982589 11:34127400 C 4076 NM_005898.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3243 rs2982589 11:34127400 C 55226 NM_001144030.1 Transcript intron_variant - - - - - - rs2982589 11:34127400 C ENSESTG00000008177 ENSESTT00000020709 Transcript intron_variant - - - - - - rs2957485 11:34130833 C 55226 NM_024662.2 Transcript intron_variant - - - - - - rs2957485 11:34130833 C CCDS44568.1 CCDS44568.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2782 rs2957485 11:34130833 C ENSESTG00000008177 ENSESTT00000020718 Transcript intron_variant - - - - - - rs2957485 11:34130833 C CCDS7889.1 CCDS7889.1 Transcript intron_variant - - - - - - rs2957485 11:34130833 C 55226 NM_001144030.1 Transcript intron_variant - - - - - - rs2957485 11:34130833 C ENSESTG00000008177 ENSESTT00000020709 Transcript intron_variant - - - - - - rs2957484 11:34132566 C 55226 NM_024662.2 Transcript intron_variant - - - - - - rs2957484 11:34132566 C CCDS44568.1 CCDS44568.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1049 rs2957484 11:34132566 C ENSESTG00000008177 ENSESTT00000020718 Transcript intron_variant - - - - - - rs2957484 11:34132566 C CCDS7889.1 CCDS7889.1 Transcript intron_variant - - - - - - rs2957484 11:34132566 C 55226 NM_001144030.1 Transcript intron_variant - - - - - - rs2957484 11:34132566 C ENSESTG00000008177 ENSESTT00000020709 Transcript intron_variant - - - - - - rs2957510 11:34142650 G ENSESTG00000008177 ENSESTT00000020718 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2957510 11:34142650 G 55226 NM_001144030.1 Transcript intron_variant - - - - - - rs2957510 11:34142650 G ENSESTG00000008177 ENSESTT00000020709 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2957510 11:34142650 G 55226 NM_024662.2 Transcript intron_variant - - - - - - rs2957510 11:34142650 G ENSESTG00000008209 ENSESTT00000020834 Transcript intron_variant - - - - - - rs2957510 11:34142650 G CCDS44568.1 CCDS44568.1 Transcript intron_variant - - - - - - rs2957510 11:34142650 G CCDS7889.1 CCDS7889.1 Transcript intron_variant - - - - - - rs2957510 11:34142650 G ENSESTG00000008209 ENSESTT00000020843 Transcript intron_variant - - - - - - rs2982618 11:34154331 G ENSESTG00000008209 ENSESTT00000020834 Transcript intron_variant - - - - - - rs2982618 11:34154331 G 55226 NM_024662.2 Transcript intron_variant - - - - - - rs2982618 11:34154331 G CCDS44568.1 CCDS44568.1 Transcript intron_variant - - - - - - rs2982618 11:34154331 G CCDS7889.1 CCDS7889.1 Transcript intron_variant - - - - - - rs2982618 11:34154331 G 55226 NM_001144030.1 Transcript intron_variant - - - - - - rs2982618 11:34154331 G ENSESTG00000008209 ENSESTT00000020843 Transcript intron_variant - - - - - - rs2957525 11:34176214 G - ENSR00000560869 RegulatoryFeature regulatory_region_variant - - - - - - rs2957525 11:34176214 G 25841 NM_145804.2 Transcript intron_variant - - - - - - rs2957525 11:34176214 G CCDS7890.2 CCDS7890.2 Transcript intron_variant - - - - - - rs423532 11:34431226 A - - - intergenic_variant - - - - - - rs515130 11:34461934 G ENSESTG00000008279 ENSESTT00000021011 Transcript intron_variant - - - - - - rs515130 11:34461934 G ENSESTG00000008279 ENSESTT00000021020 Transcript intron_variant - - - - - - rs515130 11:34461934 G 847 NM_001752.3 Transcript intron_variant - - - - - - rs515130 11:34461934 G CCDS7891.1 CCDS7891.1 Transcript intron_variant - - - - - - rs515130 11:34461934 G ENSESTG00000008279 ENSESTT00000021029 Transcript intron_variant - - - - - - rs515130 11:34461934 G ENSESTG00000008279 ENSESTT00000021033 Transcript intron_variant - - - - - - rs9943640 11:34583017 A - - - intergenic_variant - - - - - - rs550757 11:34846950 A - ENSR00000318503 RegulatoryFeature regulatory_region_variant - - - - - - rs550757 11:34846950 A - - - intergenic_variant - - - - - - rs1549790 11:34867952 G - - - intergenic_variant - - - - - - rs2732530 11:35030845 A - ENSR00000561017 RegulatoryFeature regulatory_region_variant - - - - - - rs2732530 11:35030845 A - - - intergenic_variant - - - - - - rs6484775 11:35317047 C 6506 NM_001195728.2 Transcript intron_variant - - - - - - rs6484775 11:35317047 C 6506 NM_001252652.1 Transcript intron_variant - - - - - - rs6484775 11:35317047 C CCDS55756.1 CCDS55756.1 Transcript intron_variant - - - - - - rs6484775 11:35317047 C 6506 NM_004171.3 Transcript intron_variant - - - - - - rs6484775 11:35317047 C CCDS31459.1 CCDS31459.1 Transcript intron_variant - - - - - - rs1923289 11:35432819 T 6506 NM_001195728.2 Transcript intron_variant - - - - - - rs1923289 11:35432819 T 6506 NM_001252652.1 Transcript intron_variant - - - - - - rs1923289 11:35432819 T ENSESTG00000028950 ENSESTT00000072852 Transcript intron_variant - - - - - - rs1923289 11:35432819 T 6506 NM_004171.3 Transcript intron_variant - - - - - - rs1923289 11:35432819 T ENSESTG00000028950 ENSESTT00000072896 Transcript intron_variant - - - - - - rs1923289 11:35432819 T ENSESTG00000028950 ENSESTT00000072880 Transcript intron_variant - - - - - - rs1923289 11:35432819 T CCDS31459.1 CCDS31459.1 Transcript intron_variant - - - - - - rs697318 11:35584508 C - - - intergenic_variant - - - - - - rs1512788 11:35918539 C - - - intergenic_variant - - - - - - rs262405 11:36030915 T - ENSR00000561262 RegulatoryFeature regulatory_region_variant - - - - - - rs262405 11:36030915 T 143458 NM_174902.2 Transcript intron_variant - - - - - - rs262405 11:36030915 T ENSESTG00000006760 ENSESTT00000017238 Transcript intron_variant - - - - - - rs262405 11:36030915 T ENSESTG00000006760 ENSESTT00000017164 Transcript intron_variant - - - - - - rs262405 11:36030915 T ENSESTG00000006760 ENSESTT00000017213 Transcript intron_variant - - - - - - rs262405 11:36030915 T ENSESTG00000006760 ENSESTT00000017227 Transcript intron_variant - - - - - - rs262405 11:36030915 T ENSESTG00000006760 ENSESTT00000017154 Transcript intron_variant - - - - - - rs262405 11:36030915 T ENSESTG00000006760 ENSESTT00000017222 Transcript intron_variant - - - - - - rs262405 11:36030915 T 100616311 NR_039769.1 Transcript upstream_gene_variant - - - - - - DISTANCE=733 rs262405 11:36030915 T ENSESTG00000006760 ENSESTT00000017236 Transcript intron_variant - - - - - - rs262405 11:36030915 T CCDS31462.1 CCDS31462.1 Transcript intron_variant - - - - - - rs904553 11:36070089 A - ENSR00000318565 RegulatoryFeature regulatory_region_variant - - - - - - rs904553 11:36070089 A 143458 NM_174902.2 Transcript intron_variant - - - - - - rs904553 11:36070089 A ENSESTG00000006760 ENSESTT00000017238 Transcript intron_variant - - - - - - rs904553 11:36070089 A ENSESTG00000006760 ENSESTT00000017164 Transcript intron_variant - - - - - - rs904553 11:36070089 A ENSESTG00000006760 ENSESTT00000017213 Transcript intron_variant - - - - - - rs904553 11:36070089 A ENSESTG00000006760 ENSESTT00000017227 Transcript intron_variant - - - - - - rs904553 11:36070089 A ENSESTG00000006760 ENSESTT00000017154 Transcript intron_variant - - - - - - rs904553 11:36070089 A ENSESTG00000006760 ENSESTT00000017222 Transcript intron_variant - - - - - - rs904553 11:36070089 A ENSESTG00000006760 ENSESTT00000017236 Transcript intron_variant - - - - - - rs904553 11:36070089 A CCDS31462.1 CCDS31462.1 Transcript intron_variant - - - - - - rs4756267 11:36086702 C - ENSR00001569734 RegulatoryFeature regulatory_region_variant - - - - - - rs4756267 11:36086702 C 143458 NM_174902.2 Transcript intron_variant - - - - - - rs4756267 11:36086702 C ENSESTG00000006760 ENSESTT00000017238 Transcript intron_variant - - - - - - rs4756267 11:36086702 C ENSESTG00000006760 ENSESTT00000017164 Transcript intron_variant - - - - - - rs4756267 11:36086702 C ENSESTG00000006760 ENSESTT00000017213 Transcript intron_variant - - - - - - rs4756267 11:36086702 C ENSESTG00000006760 ENSESTT00000017227 Transcript intron_variant - - - - - - rs4756267 11:36086702 C ENSESTG00000006760 ENSESTT00000017154 Transcript intron_variant - - - - - - rs4756267 11:36086702 C ENSESTG00000006760 ENSESTT00000017222 Transcript intron_variant - - - - - - rs4756267 11:36086702 C ENSESTG00000006760 ENSESTT00000017236 Transcript intron_variant - - - - - - rs4756267 11:36086702 C CCDS31462.1 CCDS31462.1 Transcript intron_variant - - - - - - rs2945719 11:36888685 G - - - intergenic_variant - - - - - - rs10742379 11:36899791 C - - - intergenic_variant - - - - - - rs7110398 11:36929082 A - - - intergenic_variant - - - - - - rs6484887 11:36948583 C - - - intergenic_variant - - - - - - rs4756358 11:36963679 C - - - intergenic_variant - - - - - - rs2422448 11:36966724 C - - - intergenic_variant - - - - - - rs1480554 11:36973150 G - - - intergenic_variant - - - - - - rs4356201 11:37532607 A - - - intergenic_variant - - - - - - rs2618286 11:37929574 G - - - intergenic_variant - - - - - - rs2618297 11:37965060 T ENSESTG00000027972 ENSESTT00000070411 Transcript intron_variant - - - - - - rs821020 11:38073548 G - - - intergenic_variant - - - - - - rs821046 11:38102473 T - - - intergenic_variant - - - - - - rs2957597 11:38123210 T - - - intergenic_variant - - - - - - rs898912 11:38332908 T - - - intergenic_variant - - - - - - rs7933611 11:38482104 C - ENSR00001569845 RegulatoryFeature regulatory_region_variant - - - - - - rs7933611 11:38482104 C - - - intergenic_variant - - - - - - rs2587723 11:38725408 G - - - intergenic_variant - - - - - - rs7938841 11:38949786 A - ENSR00001569857 RegulatoryFeature regulatory_region_variant - - - - - - rs7938841 11:38949786 A - - - intergenic_variant - - - - - - rs7110870 11:39261573 G - - - intergenic_variant - - - - - - rs12294893 11:39942923 C - - - intergenic_variant - - - - - - rs9919627 11:40055357 G - - - intergenic_variant - - - - - - rs10768612 11:40637574 G 57689 NM_001258419.1 Transcript intron_variant - - - - - - rs10768612 11:40637574 G 57689 NM_020929.2 Transcript intron_variant - - - - - - rs2922046 11:41384105 G 57689 NM_001258419.1 Transcript intron_variant - - - - - - rs2922046 11:41384105 G 57689 NM_020929.2 Transcript intron_variant - - - - - - rs287755 11:41732799 A ENSESTG00000034770 ENSESTT00000087894 Transcript intron_variant - - - - - - rs921887 11:41803020 G ENSESTG00000012050 ENSESTT00000030176 Transcript intron_variant - - - - - - rs921887 11:41803020 G ENSESTG00000012050 ENSESTT00000030177 Transcript intron_variant - - - - - - rs291722 11:41843682 C ENSESTG00000012050 ENSESTT00000030176 Transcript downstream_gene_variant - - - - - - DISTANCE=738 rs291722 11:41843682 C ENSESTG00000012050 ENSESTT00000030177 Transcript downstream_gene_variant - - - - - - DISTANCE=738 rs7130872 11:41873394 T - - - intergenic_variant - - - - - - rs1456474 11:41874094 A - - - intergenic_variant - - - - - - rs4373907 11:42158152 A - - - intergenic_variant - - - - - - rs10742624 11:42370211 G - - - intergenic_variant - - - - - - rs7482617 11:42376571 C - - - intergenic_variant - - - - - - rs6485332 11:42629229 T - - - intergenic_variant - - - - - - rs4495879 11:42913559 A - - - intergenic_variant - - - - - - rs4237641 11:43055889 G - - - intergenic_variant - - - - - - rs2220954 11:43270493 G ENSESTG00000012943 ENSESTT00000032464 Transcript intron_variant - - - - - - rs7928889 11:43367235 A 8539 NM_001243747.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1155 rs7928889 11:43367235 A ENSESTG00000012798 ENSESTT00000032181 Transcript downstream_gene_variant - - - - - - DISTANCE=2722 rs7928889 11:43367235 A 8539 NM_006595.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1155 rs7928889 11:43367235 A ENSESTG00000012798 ENSESTT00000032193 Transcript downstream_gene_variant - - - - - - DISTANCE=2138 rs7928889 11:43367235 A 8539 NR_024625.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1155 rs7928889 11:43367235 A 8539 NM_001142930.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1155 rs7928889 11:43367235 A ENSESTG00000012941 ENSESTT00000032454 Transcript intron_variant - - - - - - rs7928889 11:43367235 A CCDS44572.1 CCDS44572.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3175 rs7928889 11:43367235 A CCDS44573.1 CCDS44573.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3230 rs7928889 11:43367235 A CCDS31465.1 CCDS31465.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3230 rs7928889 11:43367235 A 8539 NM_001142931.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1155 rs1878763 11:43746999 A CCDS7905.1 CCDS7905.1 Transcript intron_variant - - - - - - rs1878763 11:43746999 A ENSESTG00000020900 ENSESTT00000052434 Transcript intron_variant - - - - - - rs1878763 11:43746999 A 51144 NM_016142.2 Transcript intron_variant - - - - - - rs1878763 11:43746999 A ENSESTG00000019382 ENSESTT00000048951 Transcript intron_variant - - - - - - rs1878763 11:43746999 A ENSESTG00000020900 ENSESTT00000052418 Transcript intron_variant - - - - - - rs1878763 11:43746999 A ENSESTG00000019382 ENSESTT00000048963 Transcript intron_variant - - - - - - rs6416124 11:44000488 G - - - intergenic_variant - - - - - - rs10838233 11:44124904 C CCDS53619.1 CCDS53619.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4359 rs10838233 11:44124904 C 2132 NM_207122.1 Transcript intron_variant - - - - - - rs10838233 11:44124904 C 2132 NM_000401.3 Transcript intron_variant - - - - - - rs10838233 11:44124904 C CCDS7908.1 CCDS7908.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4359 rs10838233 11:44124904 C 2132 NM_001178083.1 Transcript intron_variant - - - - - - rs10838233 11:44124904 C CCDS53618.1 CCDS53618.1 Transcript intron_variant - - - - - - rs10838233 11:44124904 C ENSESTG00000020136 ENSESTT00000050560 Transcript intron_variant - - - - - - rs11038035 11:44526193 C ENSESTG00000020723 ENSESTT00000051936 Transcript intron_variant - - - - - - rs782403 11:44536103 A ENSESTG00000020715 ENSESTT00000051917 Transcript downstream_gene_variant - - - - - - DISTANCE=4587 rs782403 11:44536103 A ENSESTG00000020723 ENSESTT00000051936 Transcript intron_variant - - - - - - rs1560297 11:44600408 G ENSESTG00000020471 ENSESTT00000051461 Transcript intron_variant - - - - - - rs1560297 11:44600408 G ENSESTG00000020715 ENSESTT00000051917 Transcript upstream_gene_variant - - - - - - DISTANCE=2562 rs1560297 11:44600408 G ENSESTG00000020471 ENSESTT00000051477 Transcript intron_variant - - - - - - rs1560297 11:44600408 G ENSESTG00000020471 ENSESTT00000051393 Transcript intron_variant - - - - - - rs1560297 11:44600408 G 3732 NM_002231.3 Transcript intron_variant - - - - - - rs1560297 11:44600408 G 3732 NM_001024844.1 Transcript intron_variant - - - - - - rs1560297 11:44600408 G ENSESTG00000020471 ENSESTT00000051492 Transcript intron_variant - - - - - - rs1560297 11:44600408 G ENSESTG00000020471 ENSESTT00000051499 Transcript intron_variant - - - - - - rs10769063 11:44666326 C - - - intergenic_variant - - - - - - rs4755870 11:44726184 C - - - intergenic_variant - - - - - - rs4755876 11:44739863 T ENSESTG00000033057 ENSESTT00000083531 Transcript downstream_gene_variant - - - - - - DISTANCE=1079 rs10769081 11:44794529 A ENSESTG00000032950 ENSESTT00000083342 Transcript intron_variant - - - - - - rs10769081 11:44794529 A ENSESTG00000032950 ENSESTT00000083314 Transcript intron_variant - - - - - - rs10769081 11:44794529 A 90139 NM_130783.4 Transcript intron_variant - - - - - - rs10769081 11:44794529 A ENSESTG00000032950 ENSESTT00000083336 Transcript intron_variant - - - - - - rs10769081 11:44794529 A ENSESTG00000032950 ENSESTT00000083334 Transcript intron_variant - - - - - - rs10769081 11:44794529 A ENSESTG00000032950 ENSESTT00000083323 Transcript intron_variant - - - - - - rs835995 11:44960689 G 9537 NM_001258322.1 Transcript intron_variant - - - - - - rs835995 11:44960689 G 9537 NM_001258321.1 Transcript intron_variant - - - - - - rs835995 11:44960689 G CCDS7911.1 CCDS7911.1 Transcript upstream_gene_variant - - - - - - DISTANCE=803 rs835995 11:44960689 G 9537 NM_001258320.1 Transcript 5_prime_UTR_variant 598 - - - - - rs835995 11:44960689 G ENSESTG00000033037 ENSESTT00000083524 Transcript intron_variant - - - - - - rs835995 11:44960689 G ENSESTG00000033037 ENSESTT00000083527 Transcript intron_variant - - - - - - rs835995 11:44960689 G ENSESTG00000033037 ENSESTT00000083505 Transcript intron_variant - - - - - - rs835995 11:44960689 G 9537 NM_001258323.1 Transcript intron_variant - - - - - - rs835995 11:44960689 G 9537 NM_001258324.1 Transcript intron_variant - - - - - - rs835995 11:44960689 G 9537 NM_006034.3 Transcript intron_variant - - - - - - rs7929889 11:44969896 C 9537 NM_001258322.1 Transcript intron_variant - - - - - - rs7929889 11:44969896 C 9537 NM_001258321.1 Transcript intron_variant - - - - - - rs7929889 11:44969896 C 9537 NM_001258320.1 Transcript intron_variant - - - - - - rs7929889 11:44969896 C ENSESTG00000033037 ENSESTT00000083524 Transcript intron_variant - - - - - - rs7929889 11:44969896 C ENSESTG00000033037 ENSESTT00000083527 Transcript intron_variant - - - - - - rs7929889 11:44969896 C ENSESTG00000033037 ENSESTT00000083505 Transcript intron_variant - - - - - - rs7929889 11:44969896 C 9537 NM_001258323.1 Transcript intron_variant - - - - - - rs7929889 11:44969896 C 9537 NM_001258324.1 Transcript intron_variant - - - - - - rs7929889 11:44969896 C 9537 NM_006034.3 Transcript intron_variant - - - - - - rs7930575 11:45067397 G - ENSR00000561826 RegulatoryFeature regulatory_region_variant - - - - - - rs7930575 11:45067397 G - - - intergenic_variant - - - - - - rs7395987 11:45257823 C 57586 NM_020826.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4030 rs7395987 11:45257823 C 57586 NM_001247987.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4030 rs7395987 11:45257823 C 56981 NM_001256695.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1148 rs7395987 11:45257823 C ENSESTG00000033031 ENSESTT00000083481 Transcript upstream_gene_variant - - - - - - DISTANCE=980 rs10734534 11:45630760 G - - - intergenic_variant - - - - - - rs1562457 11:45634791 C - - - intergenic_variant - - - - - - rs6416135 11:45745944 G ENSESTG00000031606 ENSESTT00000079725 Transcript downstream_gene_variant - - - - - - DISTANCE=95 rs6416135 11:45745944 G ENSESTG00000031606 ENSESTT00000079716 Transcript 3_prime_UTR_variant 385 - - - - - rs6416135 11:45745944 G 100507384 NR_047569.1 Transcript non_coding_exon_variant,nc_transcript_variant 478 - - - - - rs4755338 11:45812468 G - - - intergenic_variant - - - - - - rs10769174 11:45871481 C CCDS7915.2 CCDS7915.2 Transcript intron_variant - - - - - - rs10769174 11:45871481 C ENSESTG00000031656 ENSESTT00000079911 Transcript intron_variant - - - - - - rs10769174 11:45871481 C 1408 NM_001127457.1 Transcript intron_variant - - - - - - rs10769174 11:45871481 C 1408 NM_021117.3 Transcript intron_variant - - - - - - rs10769174 11:45871481 C CCDS44576.1 CCDS44576.1 Transcript intron_variant - - - - - - rs10769174 11:45871481 C ENSESTG00000031656 ENSESTT00000079922 Transcript intron_variant - - - - - - rs4755343 11:45883914 C CCDS7915.2 CCDS7915.2 Transcript intron_variant - - - - - - rs4755343 11:45883914 C ENSESTG00000031656 ENSESTT00000079945 Transcript intron_variant - - - - - - rs4755343 11:45883914 C ENSESTG00000031656 ENSESTT00000079911 Transcript downstream_gene_variant - - - - - - DISTANCE=255 rs4755343 11:45883914 C 1408 NM_001127457.1 Transcript intron_variant - - - - - - rs4755343 11:45883914 C 1408 NM_021117.3 Transcript intron_variant - - - - - - rs4755343 11:45883914 C CCDS44576.1 CCDS44576.1 Transcript intron_variant - - - - - - rs4756040 11:45914681 C CCDS7916.1 CCDS7916.1 Transcript intron_variant - - - - - - rs4756040 11:45914681 C ENSESTG00000031725 ENSESTT00000080067 Transcript intron_variant - - - - - - rs4756040 11:45914681 C ENSESTG00000031725 ENSESTT00000080074 Transcript upstream_gene_variant - - - - - - DISTANCE=3420 rs4756040 11:45914681 C 9479 NM_005456.3 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081913 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081856 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081929 Transcript upstream_gene_variant - - - - - - DISTANCE=3401 rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081807 Transcript intron_variant - - - - - - rs4328185 11:45994857 C CCDS44578.1 CCDS44578.1 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081898 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081919 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081840 Transcript intron_variant - - - - - - rs4328185 11:45994857 C 51317 NM_001101802.1 Transcript intron_variant - - - - - - rs4328185 11:45994857 C CCDS31474.1 CCDS31474.1 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081830 Transcript intron_variant - - - - - - rs4328185 11:45994857 C 51317 NM_016621.3 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081797 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081887 Transcript intron_variant - - - - - - rs4328185 11:45994857 C ENSESTG00000032372 ENSESTT00000081850 Transcript intron_variant - - - - - - rs9666859 11:46113512 T ENSESTG00000032372 ENSESTT00000081856 Transcript intron_variant - - - - - - rs9666859 11:46113512 T ENSESTG00000032372 ENSESTT00000081807 Transcript intron_variant - - - - - - rs9666859 11:46113512 T ENSESTG00000032372 ENSESTT00000081898 Transcript intron_variant - - - - - - rs9666859 11:46113512 T ENSESTG00000032372 ENSESTT00000081840 Transcript intron_variant - - - - - - rs9666859 11:46113512 T ENSESTG00000032372 ENSESTT00000081821 Transcript intron_variant - - - - - - rs9666859 11:46113512 T 51317 NM_001101802.1 Transcript intron_variant - - - - - - rs9666859 11:46113512 T ENSESTG00000032372 ENSESTT00000081830 Transcript intron_variant - - - - - - rs9666859 11:46113512 T 51317 NM_016621.3 Transcript intron_variant - - - - - - rs9666859 11:46113512 T ENSESTG00000032372 ENSESTT00000081797 Transcript intron_variant - - - - - - rs9666859 11:46113512 T ENSESTG00000032372 ENSESTT00000081887 Transcript intron_variant - - - - - - rs9666859 11:46113512 T ENSESTG00000032372 ENSESTT00000081850 Transcript intron_variant - - - - - - rs902284 11:46224110 C - ENSR00000561956 RegulatoryFeature regulatory_region_variant - - - - - - rs902284 11:46224110 C - - - intergenic_variant - - - - - - rs4755350 11:46237936 C - - - intergenic_variant - - - - - - rs4756068 11:46293531 G - ENSR00000685340 RegulatoryFeature regulatory_region_variant - - - - - - rs4756068 11:46293531 G - - - intergenic_variant - - - - - - rs7123865 11:46454406 C ENSESTG00000032276 ENSESTT00000081675 Transcript intron_variant - - - - - - rs7123865 11:46454406 C 55626 NM_001267783.1 Transcript intron_variant - - - - - - rs7123865 11:46454406 C ENSESTG00000032276 ENSESTT00000081585 Transcript intron_variant - - - - - - rs7123865 11:46454406 C CCDS31475.1 CCDS31475.1 Transcript intron_variant - - - - - - rs7123865 11:46454406 C ENSESTG00000032276 ENSESTT00000081646 Transcript intron_variant - - - - - - rs7123865 11:46454406 C ENSESTG00000032276 ENSESTT00000081628 Transcript intron_variant - - - - - - rs7123865 11:46454406 C 55626 NM_017749.3 Transcript intron_variant - - - - - - rs7123865 11:46454406 C CCDS58132.1 CCDS58132.1 Transcript intron_variant - - - - - - rs7123865 11:46454406 C ENSESTG00000032276 ENSESTT00000081673 Transcript intron_variant - - - - - - rs7123865 11:46454406 C 55626 NM_001267782.1 Transcript intron_variant - - - - - - rs7123865 11:46454406 C ENSESTG00000032276 ENSESTT00000081598 Transcript intron_variant - - - - - - rs7109222 11:46551117 C - ENSR00000108987 RegulatoryFeature regulatory_region_variant - - - - - - rs7109222 11:46551117 C 55626 NM_001267783.1 Transcript intron_variant - - - - - - rs7109222 11:46551117 C ENSESTG00000032276 ENSESTT00000081585 Transcript intron_variant - - - - - - rs7109222 11:46551117 C CCDS31475.1 CCDS31475.1 Transcript intron_variant - - - - - - rs7109222 11:46551117 C ENSESTG00000032276 ENSESTT00000081628 Transcript intron_variant - - - - - - rs7109222 11:46551117 C 55626 NM_017749.3 Transcript intron_variant - - - - - - rs7109222 11:46551117 C CCDS58132.1 CCDS58132.1 Transcript intron_variant - - - - - - rs7109222 11:46551117 C ENSESTG00000032276 ENSESTT00000081612 Transcript intron_variant - - - - - - rs7109222 11:46551117 C 55626 NM_001267782.1 Transcript intron_variant - - - - - - rs7109222 11:46551117 C ENSESTG00000032276 ENSESTT00000081598 Transcript intron_variant - - - - - - rs7938264 11:46767750 G CCDS7924.1 CCDS7924.1 Transcript intron_variant - - - - - - rs7938264 11:46767750 G 9793 NM_001008938.3 Transcript intron_variant - - - - - - rs7938264 11:46767750 G 9793 NM_014756.3 Transcript intron_variant - - - - - - rs7938264 11:46767750 G CCDS31477.1 CCDS31477.1 Transcript intron_variant - - - - - - rs7938264 11:46767750 G ENSESTG00000011661 ENSESTT00000029427 Transcript intron_variant - - - - - - rs1551743 11:46902661 A ENSESTG00000011569 ENSESTT00000028997 Transcript intron_variant - - - - - - rs1551743 11:46902661 A 4038 NM_002334.3 Transcript intron_variant - - - - - - rs1551743 11:46902661 A CCDS31478.1 CCDS31478.1 Transcript intron_variant - - - - - - rs1903367 11:46948508 T - - - intergenic_variant - - - - - - rs985469 11:46951949 A - ENSR00000562083 RegulatoryFeature regulatory_region_variant - - - - - - rs985469 11:46951949 A - - - intergenic_variant - - - - - - rs2867208 11:46968682 C 79096 NM_001003677.1 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027599 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027524 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027584 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027528 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027533 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027593 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027579 Transcript intron_variant - - - - - - rs2867208 11:46968682 C 79096 NM_001003678.1 Transcript intron_variant - - - - - - rs2867208 11:46968682 C CCDS31479.1 CCDS31479.1 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027468 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027597 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027592 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027540 Transcript intron_variant - - - - - - rs2867208 11:46968682 C 79096 NM_001003676.1 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027601 Transcript intron_variant - - - - - - rs2867208 11:46968682 C CCDS7925.1 CCDS7925.1 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027486 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027596 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027565 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027600 Transcript intron_variant - - - - - - rs2867208 11:46968682 C CCDS41641.1 CCDS41641.1 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027582 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027595 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027576 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027555 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027603 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027548 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027587 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027569 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027566 Transcript intron_variant - - - - - - rs2867208 11:46968682 C CCDS31480.1 CCDS31480.1 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027590 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027554 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027568 Transcript intron_variant - - - - - - rs2867208 11:46968682 C 79096 NM_024113.3 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027552 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027604 Transcript intron_variant - - - - - - rs2867208 11:46968682 C ENSESTG00000010965 ENSESTT00000027549 Transcript intron_variant - - - - - - rs901749 11:47208598 C - ENSR00000562117 RegulatoryFeature regulatory_region_variant - - - - - - rs901749 11:47208598 C 29763 NM_001184974.1 Transcript upstream_gene_variant - - - - - - DISTANCE=588 rs901749 11:47208598 C ENSESTG00000011489 ENSESTT00000028855 Transcript upstream_gene_variant - - - - - - DISTANCE=601 rs901749 11:47208598 C ENSESTG00000011489 ENSESTT00000028860 Transcript upstream_gene_variant - - - - - - DISTANCE=1628 rs901749 11:47208598 C ENSESTG00000011489 ENSESTT00000028858 Transcript upstream_gene_variant - - - - - - DISTANCE=1166 rs901749 11:47208598 C CCDS31481.1 CCDS31481.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4320 rs901749 11:47208598 C 29763 NM_001184975.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1166 rs901749 11:47208598 C 29763 NM_016223.4 Transcript upstream_gene_variant - - - - - - DISTANCE=588 rs10838676 11:47245683 T 1643 NM_000107.2 Transcript intron_variant - - - - - - rs10838676 11:47245683 T CCDS7927.1 CCDS7927.1 Transcript intron_variant - - - - - - rs10838676 11:47245683 T ENSESTG00000011027 ENSESTT00000027689 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028438 Transcript upstream_gene_variant - - - - - - DISTANCE=3576 rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028421 Transcript upstream_gene_variant - - - - - - DISTANCE=2401 rs1914401 11:47548665 T 10658 NM_001172639.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3125 rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028347 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028433 Transcript upstream_gene_variant - - - - - - DISTANCE=2439 rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028375 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028356 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028365 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028412 Transcript upstream_gene_variant - - - - - - DISTANCE=2401 rs1914401 11:47548665 T 10658 NM_006560.3 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028395 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028437 Transcript upstream_gene_variant - - - - - - DISTANCE=3576 rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028391 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028400 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028417 Transcript upstream_gene_variant - - - - - - DISTANCE=2401 rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028387 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028363 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028398 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028352 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028410 Transcript upstream_gene_variant - - - - - - DISTANCE=2401 rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028340 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028371 Transcript intron_variant - - - - - - rs1914401 11:47548665 T ENSESTG00000011278 ENSESTT00000028405 Transcript intron_variant - - - - - - rs10838737 11:47661971 C ENSESTG00000011227 ENSESTT00000028167 Transcript intron_variant - - - - - - rs10838737 11:47661971 C ENSESTG00000011227 ENSESTT00000028155 Transcript intron_variant - - - - - - rs10838737 11:47661971 C 23788 NM_014342.3 Transcript intron_variant - - - - - - rs10838737 11:47661971 C ENSESTG00000011227 ENSESTT00000028147 Transcript intron_variant - - - - - - rs10838737 11:47661971 C ENSESTG00000027266 ENSESTT00000068753 Transcript intron_variant - - - - - - rs10838737 11:47661971 C CCDS7943.1 CCDS7943.1 Transcript intron_variant - - - - - - rs7928954 11:47776047 A 23360 NM_015308.2 Transcript intron_variant - - - - - - rs7928954 11:47776047 A CCDS41644.1 CCDS41644.1 Transcript intron_variant - - - - - - rs7928954 11:47776047 A ENSESTG00000026928 ENSESTT00000068116 Transcript intron_variant - - - - - - rs7928954 11:47776047 A ENSESTG00000026928 ENSESTT00000068110 Transcript intron_variant - - - - - - rs7928954 11:47776047 A ENSESTG00000026928 ENSESTT00000068034 Transcript intron_variant - - - - - - rs7928954 11:47776047 A ENSESTG00000026928 ENSESTT00000068094 Transcript intron_variant - - - - - - rs4752869 11:47833326 T ENSESTG00000026551 ENSESTT00000066982 Transcript downstream_gene_variant - - - - - - DISTANCE=1617 rs4752869 11:47833326 T CCDS31484.1 CCDS31484.1 Transcript intron_variant - - - - - - rs4752869 11:47833326 T ENSESTG00000026696 ENSESTT00000067439 Transcript intron_variant - - - - - - rs4752869 11:47833326 T 23279 NM_015231.1 Transcript intron_variant - - - - - - rs4752869 11:47833326 T ENSESTG00000026696 ENSESTT00000067453 Transcript intron_variant - - - - - - rs1503191 11:48126254 C - ENSR00001570322 RegulatoryFeature regulatory_region_variant - - - - - - rs1503191 11:48126254 C 5795 NM_002843.3 Transcript intron_variant - - - - - - rs1503191 11:48126254 C CCDS7945.1 CCDS7945.1 Transcript intron_variant - - - - - - rs1503191 11:48126254 C CCDS44596.1 CCDS44596.1 Transcript intron_variant - - - - - - rs1503191 11:48126254 C 5795 NM_001098503.1 Transcript intron_variant - - - - - - rs4752895 11:48129861 A ENSESTG00000026346 ENSESTT00000066474 Transcript upstream_gene_variant - - - - - - DISTANCE=4484 rs4752895 11:48129861 A 5795 NM_002843.3 Transcript intron_variant - - - - - - rs4752895 11:48129861 A CCDS7945.1 CCDS7945.1 Transcript intron_variant - - - - - - rs4752895 11:48129861 A ENSESTG00000026346 ENSESTT00000066507 Transcript upstream_gene_variant - - - - - - DISTANCE=4484 rs4752895 11:48129861 A CCDS44596.1 CCDS44596.1 Transcript intron_variant - - - - - - rs4752895 11:48129861 A ENSESTG00000026346 ENSESTT00000066523 Transcript upstream_gene_variant - - - - - - DISTANCE=4484 rs4752895 11:48129861 A 5795 NM_001098503.1 Transcript intron_variant - - - - - - rs1393790 11:48265101 T CCDS31486.1 CCDS31486.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1555 rs1393790 11:48265101 T 119764 NM_001004727.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1555 rs4623932 11:48327368 G CCDS31488.1 CCDS31488.1 Transcript upstream_gene_variant - - - - - - DISTANCE=407 rs4623932 11:48327368 G 256148 NM_001004725.1 Transcript upstream_gene_variant - - - - - - DISTANCE=407 rs1586116 11:48380809 A - - - intergenic_variant - - - - - - rs1964684 11:48970095 A - - - intergenic_variant - - - - - - rs1963627 11:49005473 G 120824 NM_001206625.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2226 rs7105502 11:49392966 A - - - intergenic_variant - - - - - - rs7481551 11:49724466 T 440040 NR_027044.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4881722 11:49788478 C 440040 NR_027044.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6486025 11:49795947 A 440040 NR_027044.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs72643534 11:49834315 C 440040 NR_027044.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2344 rs72643534 11:49834315 C ENSESTG00000011410 ENSESTT00000028642 Transcript downstream_gene_variant - - - - - - DISTANCE=2772 rs6486028 11:49846626 G - - - intergenic_variant - - - - - - rs28668313 11:49977629 G 283092 NM_001001955.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2658 rs28668313 11:49977629 G CCDS31495.1 CCDS31495.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2725 rs28452996 11:50046137 T - - - intergenic_variant - - - - - - rs7937887 11:50225184 T ENSESTG00000011444 ENSESTT00000028731 Transcript downstream_gene_variant - - - - - - DISTANCE=2729 rs7101684 11:50225741 C ENSESTG00000011444 ENSESTT00000028731 Transcript downstream_gene_variant - - - - - - DISTANCE=2172 rs7946241 11:50241702 A ENSESTG00000011426 ENSESTT00000028718 Transcript intron_variant - - - - - - rs7946241 11:50241702 A ENSESTG00000011426 ENSESTT00000028707 Transcript intron_variant - - - - - - rs7946241 11:50241702 A ENSESTG00000011426 ENSESTT00000028710 Transcript intron_variant - - - - - - rs7946241 11:50241702 A ENSESTG00000011426 ENSESTT00000028672 Transcript intron_variant - - - - - - rs7946241 11:50241702 A 441601 NR_003034.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs7946241 11:50241702 A ENSESTG00000011426 ENSESTT00000028704 Transcript intron_variant - - - - - - rs690975 11:50439091 C - - - intergenic_variant - - - - - - rs485015 11:50447200 A - - - intergenic_variant - - - - - - rs8189290 11:51221495 C - - - intergenic_variant - - - - - - rs8186366 11:51297506 T - - - intergenic_variant - - - - - - rs7294234 11:51306220 T - - - intergenic_variant - - - - - - rs10794380 11:51313555 G - - - intergenic_variant - - - - - - rs545691 11:51475190 T - - - intergenic_variant - - - - - - rs490110 11:51476127 C - - - intergenic_variant - - - - - - rs4881861 11:51550102 C - - - intergenic_variant - - - - - - rs10902377 11:51555138 A - - - intergenic_variant - - - - - - rs1829873 11:54847880 A - - - intergenic_variant - - - - - - rs2704165 11:54848513 A - - - intergenic_variant - - - - - - rs9704322 11:54873975 T - - - intergenic_variant - - - - - - rs10792141 11:55138294 G CCDS31500.1 CCDS31500.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1900 rs10792141 11:55138294 G 81328 NM_001005275.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1900 rs1216214 11:55184165 T - - - intergenic_variant - - - - - - rs473123 11:55326009 C CCDS31501.1 CCDS31501.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3114 rs473123 11:55326009 C 81309 NM_001001920.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3114 rs297103 11:55545160 C CCDS31507.1 CCDS31507.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3302 rs297103 11:55545160 C 390142 NM_001001967.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3302 rs2940750 11:55583053 A CCDS31509.1 CCDS31509.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3175 rs2940750 11:55583053 A CCDS31510.1 CCDS31510.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4053 rs2940750 11:55583053 A 219437 NM_001004738.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3175 rs2940750 11:55583053 A 219438 NM_001001952.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4053 rs2512936 11:55789682 A - - - intergenic_variant - - - - - - rs2512766 11:55801266 G CCDS31516.1 CCDS31516.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2397 rs2512766 11:55801266 G 219447 NM_001001921.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2397 rs2512760 11:55803332 C CCDS31516.1 CCDS31516.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4463 rs2512760 11:55803332 C 219447 NM_001001921.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4463 rs1531763 11:55815774 T - - - intergenic_variant - - - - - - rs1871849 11:55817360 T - - - intergenic_variant - - - - - - rs2035405 11:55874103 T CCDS31518.1 CCDS31518.1 Transcript downstream_gene_variant - - - - - - DISTANCE=646 rs2035405 11:55874103 T 390151 NM_001005200.1 Transcript downstream_gene_variant - - - - - - DISTANCE=646 rs2460216 11:55879070 T - - - intergenic_variant - - - - - - rs2449141 11:55897064 A - - - intergenic_variant - - - - - - rs1481922 11:56090090 C CCDS31527.1 CCDS31527.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3369 rs1481922 11:56090090 C 219473 NM_001005202.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3369 rs1945202 11:56142231 T 219417 NM_001005204.1 Transcript upstream_gene_variant - - - - - - DISTANCE=869 rs1945202 11:56142231 T CCDS41647.1 CCDS41647.1 Transcript upstream_gene_variant - - - - - - DISTANCE=869 rs1945194 11:56147204 T 219417 NM_001005204.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3175 rs1945194 11:56147204 T CCDS41647.1 CCDS41647.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3175 rs631962 11:56256147 T 219484 NM_001005282.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1764 rs631962 11:56256147 T CCDS31533.1 CCDS31533.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1764 rs587256 11:56289539 T - ENSR00000562603 RegulatoryFeature regulatory_region_variant - - - - - - rs587256 11:56289539 T - - - intergenic_variant - - - - - - rs646472 11:56294338 A - - - intergenic_variant - - - - - - rs7944995 11:56361390 A - - - intergenic_variant - - - - - - rs61696591 11:56364573 C - - - intergenic_variant - - - - - - rs1510002 11:56371946 A - - - intergenic_variant - - - - - - rs1876925 11:56422196 G - - - intergenic_variant - - - - - - rs1397055 11:56428113 G 219493 NM_001004730.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3049 rs1397055 11:56428113 G CCDS31535.1 CCDS31535.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3049 rs11228714 11:56438992 A - - - intergenic_variant - - - - - - rs525257 11:56560416 A - - - intergenic_variant - - - - - - rs513179 11:56581025 T - - - intergenic_variant - - - - - - rs579126 11:56590150 A - - - intergenic_variant - - - - - - rs1792514 11:56677672 T - - - intergenic_variant - - - - - - rs1945997 11:56743142 G - - - intergenic_variant - - - - - - rs1946000 11:56749904 A - - - intergenic_variant - - - - - - rs2853075 11:56795280 A - - - intergenic_variant - - - - - - rs2853076 11:56800716 T 219525 NR_036445.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4293 rs1943490 11:56953812 G CCDS31539.1 CCDS31539.1 Transcript intron_variant - - - - - - rs1943490 11:56953812 G 219527 NM_001005210.2 Transcript intron_variant - - - - - - rs1943487 11:56957775 A CCDS31539.1 CCDS31539.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2821 rs1943487 11:56957775 A 219527 NM_001005210.2 Transcript 3_prime_UTR_variant 3994 - - - - - rs948848 11:56965739 T - - - intergenic_variant - - - - - - rs7114596 11:56969519 G - - - intergenic_variant - - - - - - rs7102922 11:56971248 A - ENSR00000562635 RegulatoryFeature regulatory_region_variant - - - - - - rs7102922 11:56971248 A - - - intergenic_variant - - - - - - rs4939112 11:56973093 T - - - intergenic_variant - - - - - - rs7101929 11:56983648 C - - - intergenic_variant - - - - - - rs4939114 11:56988352 G - - - intergenic_variant - - - - - - rs2432809 11:57368598 G 710 NM_001032295.1 Transcript intron_variant - - - - - - rs2432809 11:57368598 G CCDS7962.1 CCDS7962.1 Transcript intron_variant - - - - - - rs2432809 11:57368598 G ENSESTG00000012079 ENSESTT00000030262 Transcript downstream_gene_variant - - - - - - DISTANCE=860 rs2432809 11:57368598 G 710 NM_000062.2 Transcript intron_variant - - - - - - rs2432809 11:57368598 G ENSESTG00000012099 ENSESTT00000030285 Transcript intron_variant - - - - - - rs2432809 11:57368598 G ENSESTG00000012079 ENSESTT00000030253 Transcript downstream_gene_variant - - - - - - DISTANCE=860 rs2432809 11:57368598 G ENSESTG00000012099 ENSESTT00000030289 Transcript intron_variant - - - - - - rs616989 11:57654156 T - - - intergenic_variant - - - - - - rs7131291 11:57654928 A - - - intergenic_variant - - - - - - rs1447175 11:57860056 A 219956 NM_001005212.3 Transcript intron_variant - - - - - - rs2443435 11:57861876 C 219956 NM_001005212.3 Transcript intron_variant - - - - - - rs4939194 11:58004386 C - - - intergenic_variant - - - - - - rs7930186 11:58129677 C CCDS31548.1 CCDS31548.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3135 rs7930186 11:58129677 C 219965 NM_001005489.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3135 rs4373953 11:58190867 C 390190 NM_001005566.2 Transcript upstream_gene_variant - - - - - - DISTANCE=81 rs4373953 11:58190867 C CCDS31550.1 CCDS31550.1 Transcript upstream_gene_variant - - - - - - DISTANCE=133 rs663721 11:58393922 G - ENSR00001570449 RegulatoryFeature regulatory_region_variant - - - - - - rs663721 11:58393922 G 386607 NR_024091.1 Transcript downstream_gene_variant - - - - - - DISTANCE=716 rs663721 11:58393922 G ENSESTG00000035221 ENSESTT00000088967 Transcript downstream_gene_variant - - - - - - DISTANCE=1122 rs663721 11:58393922 G 80829 NM_053023.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4899 rs663721 11:58393922 G CCDS31554.1 CCDS31554.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1927 rs663721 11:58393922 G 80829 NM_001197051.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4899 rs663721 11:58393922 G 1270 NM_000614.3 Transcript downstream_gene_variant - - - - - - DISTANCE=716 rs519516 11:58927679 G - - - intergenic_variant - - - - - - rs7106463 11:59369401 G ENSESTG00000012223 ENSESTT00000030636 Transcript intron_variant - - - - - - rs7106463 11:59369401 G ENSESTG00000012223 ENSESTT00000030633 Transcript intron_variant - - - - - - rs7106463 11:59369401 G 5007 NM_002556.2 Transcript intron_variant - - - - - - rs7106463 11:59369401 G ENSESTG00000012223 ENSESTT00000030641 Transcript intron_variant - - - - - - rs7106463 11:59369401 G CCDS7974.1 CCDS7974.1 Transcript intron_variant - - - - - - rs7106463 11:59369401 G ENSESTG00000012223 ENSESTT00000030591 Transcript intron_variant - - - - - - rs1303605 11:59881728 G - - - intergenic_variant - - - - - - rs3018806 11:60073702 T - ENSR00001570518 RegulatoryFeature regulatory_region_variant - - - - - - rs3018806 11:60073702 T CCDS58135.1 CCDS58135.1 Transcript intron_variant - - - - - - rs3018806 11:60073702 T 51338 NM_148975.2 Transcript intron_variant - - - - - - rs3018806 11:60073702 T 51338 NM_024021.3 Transcript intron_variant - - - - - - rs3018806 11:60073702 T CCDS7982.1 CCDS7982.1 Transcript intron_variant - - - - - - rs3018806 11:60073702 T ENSESTG00000009925 ENSESTT00000024825 Transcript intron_variant - - - - - - rs3018806 11:60073702 T 51338 NM_001243266.1 Transcript intron_variant - - - - - - rs7102411 11:60187638 A 84689 NR_049734.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2409 rs7102411 11:60187638 A 84689 NR_049733.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2409 rs7102411 11:60187638 A 84689 NR_049731.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2409 rs7102411 11:60187638 A ENSESTG00000009976 ENSESTT00000024962 Transcript downstream_gene_variant - - - - - - DISTANCE=4695 rs7102411 11:60187638 A CCDS58136.1 CCDS58136.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3157 rs7102411 11:60187638 A CCDS31569.1 CCDS31569.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3157 rs7102411 11:60187638 A 84689 NM_001261827.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2409 rs7102411 11:60187638 A 84689 NR_049732.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2409 rs7102411 11:60187638 A 84689 NM_001261828.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2409 rs7102411 11:60187638 A 84689 NM_001079692.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2409 rs7102411 11:60187638 A CCDS41652.1 CCDS41652.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3157 rs7102411 11:60187638 A ENSESTG00000009976 ENSESTT00000024958 Transcript downstream_gene_variant - - - - - - DISTANCE=4010 rs7102411 11:60187638 A 84689 NM_032597.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2409 rs7950299 11:60194310 G ENSESTG00000009997 ENSESTT00000025007 Transcript upstream_gene_variant - - - - - - DISTANCE=2752 rs7950299 11:60194310 G CCDS7987.1 CCDS7987.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2838 rs7950299 11:60194310 G ENSESTG00000009997 ENSESTT00000025016 Transcript upstream_gene_variant - - - - - - DISTANCE=2927 rs7950299 11:60194310 G 64232 NM_023945.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2752 rs7950299 11:60194310 G ENSESTG00000009997 ENSESTT00000025010 Transcript upstream_gene_variant - - - - - - DISTANCE=2782 rs10736705 11:60200889 T ENSESTG00000009997 ENSESTT00000025007 Transcript intron_variant - - - - - - rs10736705 11:60200889 T CCDS7987.1 CCDS7987.1 Transcript intron_variant - - - - - - rs10736705 11:60200889 T ENSESTG00000009997 ENSESTT00000025016 Transcript intron_variant - - - - - - rs10736705 11:60200889 T 64232 NM_023945.2 Transcript intron_variant - - - - - - rs10736705 11:60200889 T ENSESTG00000009997 ENSESTT00000025010 Transcript intron_variant - - - - - - rs894590 11:60202747 A ENSESTG00000009997 ENSESTT00000025007 Transcript intron_variant - - - - - - rs894590 11:60202747 A CCDS7987.1 CCDS7987.1 Transcript intron_variant - - - - - - rs894590 11:60202747 A ENSESTG00000009997 ENSESTT00000025016 Transcript intron_variant - - - - - - rs894590 11:60202747 A 64232 NM_023945.2 Transcript intron_variant - - - - - - rs894590 11:60202747 A ENSESTG00000009997 ENSESTT00000025010 Transcript downstream_gene_variant - - - - - - DISTANCE=1409 rs1443244 11:60211877 G ENSESTG00000009997 ENSESTT00000025007 Transcript intron_variant - - - - - - rs1443244 11:60211877 G CCDS7987.1 CCDS7987.1 Transcript intron_variant - - - - - - rs1443244 11:60211877 G ENSESTG00000009997 ENSESTT00000025016 Transcript intron_variant - - - - - - rs1443244 11:60211877 G 64232 NM_023945.2 Transcript intron_variant - - - - - - rs10736708 11:60361905 A - - - intergenic_variant - - - - - - rs511597 11:60500413 C ENSESTG00000010070 ENSESTT00000025204 Transcript upstream_gene_variant - - - - - - DISTANCE=608 rs511597 11:60500413 C 728588 XM_001715696.4 Transcript intron_variant - - - - - - rs566411 11:60638470 G CCDS31572.1 CCDS31572.1 Transcript synonymous_variant 867 867 289 V gtA/gtG - rs566411 11:60638470 G ENSESTG00000002292 ENSESTT00000005714 Transcript upstream_gene_variant - - - - - - DISTANCE=2181 rs566411 11:60638470 G ENSESTG00000002292 ENSESTT00000005711 Transcript upstream_gene_variant - - - - - - DISTANCE=2128 rs566411 11:60638470 G ENSESTG00000002292 ENSESTT00000005707 Transcript 5_prime_UTR_variant 157 - - - - - rs566411 11:60638470 G 22917 NM_207341.2 Transcript synonymous_variant 887 867 289 V gtA/gtG - rs10750950 11:60746857 C - ENSR00000563061 RegulatoryFeature regulatory_region_variant - - - - - - rs10750950 11:60746857 C CCDS7999.1 CCDS7999.1 Transcript intron_variant - - - - - - rs10750950 11:60746857 C CCDS58137.1 CCDS58137.1 Transcript intron_variant - - - - - - rs10750950 11:60746857 C ENSESTG00000002394 ENSESTT00000005967 Transcript intron_variant - - - - - - rs10750950 11:60746857 C ENSESTG00000002394 ENSESTT00000005982 Transcript intron_variant - - - - - - rs10750950 11:60746857 C CCDS58138.1 CCDS58138.1 Transcript intron_variant - - - - - - rs10750950 11:60746857 C 923 NM_001254751.1 Transcript intron_variant - - - - - - rs10750950 11:60746857 C 923 NM_006725.4 Transcript intron_variant - - - - - - rs10750950 11:60746857 C 923 NR_045638.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10750950 11:60746857 C 923 NM_001254750.1 Transcript intron_variant - - - - - - rs10750950 11:60746857 C ENSESTG00000002394 ENSESTT00000005960 Transcript intron_variant - - - - - - rs10750950 11:60746857 C ENSESTG00000002394 ENSESTT00000005979 Transcript intron_variant - - - - - - rs574747 11:60870407 G CCDS8000.1 CCDS8000.1 Transcript intron_variant - - - - - - rs574747 11:60870407 G 921 NM_014207.3 Transcript intron_variant - - - - - - rs574747 11:60870407 G ENSESTG00000002430 ENSESTT00000006055 Transcript intron_variant - - - - - - rs418304 11:61740641 C - ENSR00000563214 RegulatoryFeature regulatory_region_variant - - - - - - rs418304 11:61740641 C - PB0134.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_NAME=Jaspar_Matrix_HNF4A:PB0134.1;HIGH_INF_POS=N rs418304 11:61740641 C - - - intergenic_variant - - - - - - rs367961 11:61846565 C ENSESTG00000000924 ENSESTT00000002220 Transcript intron_variant - - - - - - rs2513068 11:62216788 C - ENSR00000563290 RegulatoryFeature regulatory_region_variant - - - - - - rs2513068 11:62216788 C ENSESTG00000000896 ENSESTT00000002195 Transcript intron_variant - - - - - - rs2513068 11:62216788 C CCDS44625.1 CCDS44625.1 Transcript intron_variant - - - - - - rs2513068 11:62216788 C 79026 NM_024060.2 Transcript intron_variant - - - - - - rs2513068 11:62216788 C ENSESTG00000000896 ENSESTT00000002197 Transcript intron_variant - - - - - - rs2428542 11:62254269 T ENSESTG00000000896 ENSESTT00000002195 Transcript intron_variant - - - - - - rs2428542 11:62254269 T CCDS44625.1 CCDS44625.1 Transcript intron_variant - - - - - - rs2428542 11:62254269 T 79026 NM_024060.2 Transcript intron_variant - - - - - - rs2428542 11:62254269 T ENSESTG00000000896 ENSESTT00000002197 Transcript intron_variant - - - - - - rs2512558 11:62359968 T - ENSR00000188902 RegulatoryFeature regulatory_region_variant - - - - - - rs2512558 11:62359968 T 9219 NM_004739.3 Transcript downstream_gene_variant - - - - - - DISTANCE=707 rs2512558 11:62359968 T 64852 NM_022830.2 Transcript upstream_gene_variant - - - - - - DISTANCE=859 rs2512558 11:62359968 T CCDS8022.1 CCDS8022.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1379 rs2512558 11:62359968 T ENSESTG00000000834 ENSESTT00000002010 Transcript upstream_gene_variant - - - - - - DISTANCE=922 rs2512558 11:62359968 T ENSESTG00000000834 ENSESTT00000002009 Transcript upstream_gene_variant - - - - - - DISTANCE=914 rs2512558 11:62359968 T CCDS8021.2 CCDS8021.2 Transcript upstream_gene_variant - - - - - - DISTANCE=897 rs524891 11:62619000 G - ENSR00000685533 RegulatoryFeature regulatory_region_variant - - - - - - rs524891 11:62619000 G 9298 NR_002560.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1798 rs524891 11:62619000 G 6520 NM_001012664.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4484 rs524891 11:62619000 G ENSESTG00000016557 ENSESTT00000041546 Transcript downstream_gene_variant - - - - - - DISTANCE=730 rs524891 11:62619000 G ENSESTG00000016557 ENSESTT00000041579 Transcript downstream_gene_variant - - - - - - DISTANCE=466 rs524891 11:62619000 G CCDS31589.1 CCDS31589.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4742 rs524891 11:62619000 G 9299 NR_002561.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2135 rs524891 11:62619000 G 9303 NR_002565.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4037 rs524891 11:62619000 G CCDS31588.1 CCDS31588.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4742 rs524891 11:62619000 G 9302 NR_002564.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3764 rs524891 11:62619000 G 9301 NR_002563.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3484 rs524891 11:62619000 G 9297 NR_002559.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2376 rs524891 11:62619000 G CCDS8039.2 CCDS8039.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4742 rs524891 11:62619000 G 9304 NR_000008.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1382 rs524891 11:62619000 G 23642 NR_003098.1 Transcript downstream_gene_variant - - - - - - DISTANCE=460 rs524891 11:62619000 G 6520 NM_002394.5 Transcript upstream_gene_variant - - - - - - DISTANCE=4484 rs524891 11:62619000 G 9300 NR_002562.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3093 rs524891 11:62619000 G ENSESTG00000016162 ENSESTT00000040562 Transcript upstream_gene_variant - - - - - - DISTANCE=4484 rs524891 11:62619000 G 6520 NM_001012662.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4484 rs10897317 11:62790010 G - - - intergenic_variant - - - - - - rs2155323 11:62811248 C - - - intergenic_variant - - - - - - rs10897344 11:62858320 C 283238 NM_001136506.2 Transcript intron_variant - - - - - - rs1939762 11:62928587 G ENSESTG00000016496 ENSESTT00000041359 Transcript downstream_gene_variant - - - - - - DISTANCE=3452 rs1939762 11:62928587 G 387601 NM_199352.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2709 rs1939762 11:62928587 G CCDS31592.1 CCDS31592.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2709 rs1300800 11:62975961 G 387601 NM_199352.3 Transcript intron_variant - - - - - - rs1300800 11:62975961 G CCDS31592.1 CCDS31592.1 Transcript intron_variant - - - - - - rs584905 11:63313644 C CCDS41662.1 CCDS41662.1 Transcript synonymous_variant 411 411 137 V gtT/gtC - rs584905 11:63313644 C ENSESTG00000016281 ENSESTT00000040900 Transcript missense_variant 776 47 16 L/S tTg/tCg - rs584905 11:63313644 C ENSESTG00000016281 ENSESTT00000040894 Transcript downstream_gene_variant - - - - - - DISTANCE=1131 rs584905 11:63313644 C 5920 NM_004585.3 Transcript synonymous_variant 479 411 137 V gtT/gtC - rs584905 11:63313644 C ENSESTG00000016281 ENSESTT00000040886 Transcript synonymous_variant 452 411 137 V gtT/gtC - rs56315049 11:63381847 C - ENSR00000563467 RegulatoryFeature regulatory_region_variant - - - - - - rs56315049 11:63381847 C ENSESTG00000016416 ENSESTT00000041224 Transcript 5_prime_UTR_variant 59 - - - - - rs56315049 11:63381847 C ENSESTG00000016416 ENSESTT00000041237 Transcript upstream_gene_variant - - - - - - DISTANCE=26 rs56315049 11:63381847 C ENSESTG00000016416 ENSESTT00000041178 Transcript intron_variant - - - - - - rs56315049 11:63381847 C 11145 NM_001128203.1 Transcript intron_variant - - - - - - rs56315049 11:63381847 C ENSESTG00000016416 ENSESTT00000041210 Transcript intron_variant - - - - - - rs56315049 11:63381847 C 11145 NM_007069.3 Transcript 5_prime_UTR_variant 63 - - - - - rs56315049 11:63381847 C CCDS8047.1 CCDS8047.1 Transcript upstream_gene_variant - - - - - - DISTANCE=361 rs56315049 11:63381847 C ENSESTG00000016308 ENSESTT00000040910 Transcript upstream_gene_variant - - - - - - DISTANCE=1941 rs597994 11:63417270 A 25923 NM_015459.3 Transcript intron_variant - - - - - - rs597994 11:63417270 A ENSESTG00000016313 ENSESTT00000040923 Transcript intron_variant - - - - - - rs597994 11:63417270 A CCDS41663.1 CCDS41663.1 Transcript intron_variant - - - - - - rs597994 11:63417270 A ENSESTG00000016380 ENSESTT00000041117 Transcript intron_variant - - - - - - rs9667267 11:63542693 G - - - intergenic_variant - - - - - - rs224171 11:63651538 C ENSESTG00000026870 ENSESTT00000067708 Transcript upstream_gene_variant - - - - - - DISTANCE=4449 rs224171 11:63651538 C ENSESTG00000026870 ENSESTT00000067736 Transcript upstream_gene_variant - - - - - - DISTANCE=4481 rs224171 11:63651538 C 2011 NM_004954.4 Transcript intron_variant - - - - - - rs224171 11:63651538 C CCDS8051.2 CCDS8051.2 Transcript intron_variant - - - - - - rs224171 11:63651538 C 2011 NM_001039469.2 Transcript intron_variant - - - - - - rs224171 11:63651538 C CCDS53650.1 CCDS53650.1 Transcript intron_variant - - - - - - rs224171 11:63651538 C CCDS53651.1 CCDS53651.1 Transcript intron_variant - - - - - - rs224171 11:63651538 C CCDS53649.1 CCDS53649.1 Transcript intron_variant - - - - - - rs224171 11:63651538 C 2011 NM_017490.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4449 rs224171 11:63651538 C 2011 NM_001163297.1 Transcript intron_variant - - - - - - rs224171 11:63651538 C 2011 NM_001163296.1 Transcript intron_variant - - - - - - rs224172 11:63652378 G ENSESTG00000026870 ENSESTT00000067708 Transcript upstream_gene_variant - - - - - - DISTANCE=3609 rs224172 11:63652378 G ENSESTG00000026870 ENSESTT00000067736 Transcript upstream_gene_variant - - - - - - DISTANCE=3641 rs224172 11:63652378 G 2011 NM_004954.4 Transcript intron_variant - - - - - - rs224172 11:63652378 G CCDS8051.2 CCDS8051.2 Transcript intron_variant - - - - - - rs224172 11:63652378 G 2011 NM_001039469.2 Transcript intron_variant - - - - - - rs224172 11:63652378 G CCDS53650.1 CCDS53650.1 Transcript intron_variant - - - - - - rs224172 11:63652378 G CCDS53651.1 CCDS53651.1 Transcript intron_variant - - - - - - rs224172 11:63652378 G CCDS53649.1 CCDS53649.1 Transcript intron_variant - - - - - - rs224172 11:63652378 G 2011 NM_017490.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3609 rs224172 11:63652378 G 2011 NM_001163297.1 Transcript intron_variant - - - - - - rs224172 11:63652378 G 2011 NM_001163296.1 Transcript intron_variant - - - - - - rs6591827 11:63696054 T - - - intergenic_variant - - - - - - rs505421 11:63746418 G ENSESTG00000029070 ENSESTT00000073196 Transcript upstream_gene_variant - - - - - - DISTANCE=2406 rs505421 11:63746418 G CCDS8054.1 CCDS8054.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2626 rs505421 11:63746418 G 1351 NM_004074.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2403 rs505421 11:63746418 G ENSESTG00000027089 ENSESTT00000068299 Transcript downstream_gene_variant - - - - - - DISTANCE=2403 rs2248594 11:63874963 G ENSESTG00000027182 ENSESTT00000068512 Transcript downstream_gene_variant - - - - - - DISTANCE=3916 rs2248594 11:63874963 G ENSESTG00000028974 ENSESTT00000073071 Transcript intron_variant - - - - - - rs2248594 11:63874963 G 28992 NM_014067.3 Transcript intron_variant - - - - - - rs2248594 11:63874963 G 23769 NM_013280.4 Transcript intron_variant - - - - - - rs2248594 11:63874963 G ENSESTG00000028974 ENSESTT00000073000 Transcript intron_variant - - - - - - rs2248594 11:63874963 G CCDS8056.1 CCDS8056.1 Transcript intron_variant - - - - - - rs2248594 11:63874963 G ENSESTG00000027182 ENSESTT00000068524 Transcript downstream_gene_variant - - - - - - DISTANCE=3810 rs2248594 11:63874963 G ENSESTG00000027207 ENSESTT00000068548 Transcript intron_variant - - - - - - rs2248594 11:63874963 G ENSESTG00000027182 ENSESTT00000068532 Transcript downstream_gene_variant - - - - - - DISTANCE=3978 rs2429456 11:63994696 C 84304 NM_001128613.1 Transcript intron_variant - - - - - - rs2429456 11:63994696 C 83707 NM_001160390.1 Transcript upstream_gene_variant - - - - - - DISTANCE=970 rs2429456 11:63994696 C 83706 NM_031471.5 Transcript downstream_gene_variant - - - - - - DISTANCE=3333 rs2429456 11:63994696 C ENSESTG00000027495 ENSESTT00000069323 Transcript intron_variant - - - - - - rs2429456 11:63994696 C 83707 NM_001160389.1 Transcript upstream_gene_variant - - - - - - DISTANCE=970 rs2429456 11:63994696 C 83706 NM_178443.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3333 rs2429456 11:63994696 C ENSESTG00000027551 ENSESTT00000069355 Transcript upstream_gene_variant - - - - - - DISTANCE=3324 rs2429456 11:63994696 C ENSESTG00000027366 ENSESTT00000069099 Transcript downstream_gene_variant - - - - - - DISTANCE=3570 rs2429456 11:63994696 C 84304 NM_032344.2 Transcript intron_variant - - - - - - rs2429456 11:63994696 C ENSESTG00000027366 ENSESTT00000069165 Transcript downstream_gene_variant - - - - - - DISTANCE=3570 rs2429456 11:63994696 C 83707 NM_001160392.1 Transcript upstream_gene_variant - - - - - - DISTANCE=970 rs2429456 11:63994696 C ENSESTG00000027366 ENSESTT00000069187 Transcript downstream_gene_variant - - - - - - DISTANCE=3570 rs2429456 11:63994696 C CCDS44639.1 CCDS44639.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1716 rs2429456 11:63994696 C CCDS8060.1 CCDS8060.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3732 rs2429456 11:63994696 C ENSESTG00000028894 ENSESTT00000072721 Transcript downstream_gene_variant - - - - - - DISTANCE=3398 rs2429456 11:63994696 C 84304 NM_001128612.1 Transcript intron_variant - - - - - - rs2429456 11:63994696 C CCDS44640.1 CCDS44640.1 Transcript intron_variant - - - - - - rs2429456 11:63994696 C ENSESTG00000028903 ENSESTT00000072878 Transcript upstream_gene_variant - - - - - - DISTANCE=990 rs2429456 11:63994696 C ENSESTG00000027495 ENSESTT00000069224 Transcript intron_variant - - - - - - rs2429456 11:63994696 C CCDS53652.1 CCDS53652.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1364 rs2429456 11:63994696 C CCDS8059.1 CCDS8059.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3732 rs2429456 11:63994696 C 83707 NM_001160393.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1355 rs2429456 11:63994696 C 83707 NM_031472.3 Transcript upstream_gene_variant - - - - - - DISTANCE=970 rs2429456 11:63994696 C 3338 NM_005528.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3057 rs2429456 11:63994696 C 83707 NM_001033678.3 Transcript upstream_gene_variant - - - - - - DISTANCE=970 rs2429456 11:63994696 C ENSESTG00000028903 ENSESTT00000072898 Transcript upstream_gene_variant - - - - - - DISTANCE=1060 rs2429456 11:63994696 C CCDS41666.1 CCDS41666.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3631 rs2429456 11:63994696 C ENSESTG00000028903 ENSESTT00000072856 Transcript upstream_gene_variant - - - - - - DISTANCE=990 rs2429456 11:63994696 C ENSESTG00000027366 ENSESTT00000069177 Transcript downstream_gene_variant - - - - - - DISTANCE=4033 rs2429456 11:63994696 C CCDS31595.1 CCDS31595.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1364 rs2429456 11:63994696 C CCDS53653.1 CCDS53653.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1364 rs2429456 11:63994696 C ENSESTG00000028894 ENSESTT00000072705 Transcript downstream_gene_variant - - - - - - DISTANCE=2181 rs2429456 11:63994696 C ENSESTG00000027551 ENSESTT00000069434 Transcript upstream_gene_variant - - - - - - DISTANCE=3346 rs2429456 11:63994696 C CCDS8061.1 CCDS8061.1 Transcript intron_variant - - - - - - rs679730 11:64084113 G CCDS8068.1 CCDS8068.1 Transcript downstream_gene_variant - - - - - - DISTANCE=220 rs679730 11:64084113 G CCDS41667.1 CCDS41667.1 Transcript downstream_gene_variant - - - - - - DISTANCE=675 rs679730 11:64084113 G 25824 NM_181652.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1447 rs679730 11:64084113 G 2101 NM_004451.3 Transcript 3_prime_UTR_variant 2124 - - - - - rs679730 11:64084113 G ENSESTG00000028060 ENSESTT00000070717 Transcript upstream_gene_variant - - - - - - DISTANCE=1497 rs679730 11:64084113 G ENSESTG00000028031 ENSESTT00000070564 Transcript missense_variant 138 106 36 T/A Act/Gct - rs679730 11:64084113 G 51504 NM_016404.1 Transcript downstream_gene_variant - - - - - - DISTANCE=50 rs679730 11:64084113 G 25824 NM_012094.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1447 rs679730 11:64084113 G CCDS8071.1 CCDS8071.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1575 rs679730 11:64084113 G 25824 NM_181651.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1447 rs679730 11:64084113 G CCDS8070.1 CCDS8070.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1575 rs679730 11:64084113 G CCDS8069.1 CCDS8069.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1575 rs489419 11:64120435 C 283234 NM_032251.5 Transcript intron_variant - - - - - - rs489419 11:64120435 C ENSESTG00000028140 ENSESTT00000070927 Transcript intron_variant - - - - - - rs489419 11:64120435 C ENSESTG00000028140 ENSESTT00000070972 Transcript upstream_gene_variant - - - - - - DISTANCE=2380 rs489419 11:64120435 C ENSESTG00000028140 ENSESTT00000070903 Transcript intron_variant - - - - - - rs489419 11:64120435 C ENSESTG00000028140 ENSESTT00000070957 Transcript upstream_gene_variant - - - - - - DISTANCE=823 rs489419 11:64120435 C CCDS8072.2 CCDS8072.2 Transcript intron_variant - - - - - - rs181278 11:64229695 G - - - intergenic_variant - - - - - - rs1209687 11:64343253 C ENSESTG00000028376 ENSESTT00000071375 Transcript intron_variant - - - - - - rs1209687 11:64343253 C CCDS8074.1 CCDS8074.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4739 rs1209687 11:64343253 C 55867 NM_018484.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4254 rs1209687 11:64343253 C ENSESTG00000028376 ENSESTT00000071380 Transcript downstream_gene_variant - - - - - - DISTANCE=4298 rs1207213 11:64423842 G - ENSR00000109792 RegulatoryFeature regulatory_region_variant - - - - - - rs1207213 11:64423842 G 9379 NM_138732.2 Transcript intron_variant - - - - - - rs1207213 11:64423842 G ENSESTG00000028723 ENSESTT00000072358 Transcript upstream_gene_variant - - - - - - DISTANCE=250 rs1207213 11:64423842 G ENSESTG00000028723 ENSESTT00000072321 Transcript intron_variant - - - - - - rs1207213 11:64423842 G ENSESTG00000028723 ENSESTT00000072313 Transcript intron_variant - - - - - - rs1207213 11:64423842 G ENSESTG00000028701 ENSESTT00000072225 Transcript downstream_gene_variant - - - - - - DISTANCE=4447 rs1207213 11:64423842 G ENSESTG00000028418 ENSESTT00000071409 Transcript intron_variant - - - - - - rs1207213 11:64423842 G CCDS8077.1 CCDS8077.1 Transcript intron_variant - - - - - - rs1207213 11:64423842 G ENSESTG00000028723 ENSESTT00000072378 Transcript upstream_gene_variant - - - - - - DISTANCE=446 rs1207213 11:64423842 G ENSESTG00000028376 ENSESTT00000071375 Transcript intron_variant - - - - - - rs1207213 11:64423842 G 9379 NM_015080.3 Transcript intron_variant - - - - - - rs1207213 11:64423842 G CCDS31597.1 CCDS31597.1 Transcript intron_variant - - - - - - rs1152629 11:64447353 G ENSESTG00000028687 ENSESTT00000072185 Transcript intron_variant - - - - - - rs1152629 11:64447353 G 9379 NM_138732.2 Transcript intron_variant - - - - - - rs1152629 11:64447353 G CCDS8077.1 CCDS8077.1 Transcript intron_variant - - - - - - rs1152629 11:64447353 G ENSESTG00000028376 ENSESTT00000071375 Transcript intron_variant - - - - - - rs1152629 11:64447353 G CCDS31597.1 CCDS31597.1 Transcript intron_variant - - - - - - rs1152629 11:64447353 G 9379 NM_015080.3 Transcript intron_variant - - - - - - rs541525 11:64605689 G 55561 NM_017525.2 Transcript intron_variant - - - - - - rs541525 11:64605689 G CCDS31601.1 CCDS31601.1 Transcript intron_variant - - - - - - rs1633463 11:64611639 G - ENSR00000563705 RegulatoryFeature regulatory_region_variant - - - - - - rs1633463 11:64611639 G 55561 NM_017525.2 Transcript intron_variant - - - - - - rs1633463 11:64611639 G CCDS31601.1 CCDS31601.1 Transcript intron_variant - - - - - - rs3897618 11:64621856 G 10938 NM_006795.2 Transcript synonymous_variant 1809 1554 518 P ccT/ccC - rs3897618 11:64621856 G ENSESTG00000029208 ENSESTT00000073590 Transcript intron_variant - - - - - - rs3897618 11:64621856 G ENSESTG00000029208 ENSESTT00000073556 Transcript intron_variant - - - - - - rs3897618 11:64621856 G CCDS8084.1 CCDS8084.1 Transcript synonymous_variant 1554 1554 518 P ccT/ccC - rs3897618 11:64621856 G ENSESTG00000026304 ENSESTT00000066281 Transcript downstream_gene_variant - - - - - - DISTANCE=1104 rs3897618 11:64621856 G ENSESTG00000029208 ENSESTT00000073574 Transcript downstream_gene_variant - - - - - - DISTANCE=121 rs3897618 11:64621856 G ENSESTG00000029208 ENSESTT00000073602 Transcript intron_variant - - - - - - rs1152608 11:64844809 G 113130 NM_080668.3 Transcript downstream_gene_variant - - - - - - DISTANCE=118 rs1152608 11:64844809 G ENSESTG00000028861 ENSESTT00000072627 Transcript intron_variant - - - - - - rs1152608 11:64844809 G ENSESTG00000028831 ENSESTT00000072587 Transcript downstream_gene_variant - - - - - - DISTANCE=2141 rs1152608 11:64844809 G CCDS8091.1 CCDS8091.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1770 rs1152608 11:64844809 G ENSESTG00000028831 ENSESTT00000072576 Transcript downstream_gene_variant - - - - - - DISTANCE=2141 rs2844286 11:64869703 T - ENSR00000563748 RegulatoryFeature regulatory_region_variant - - - - - - rs2844286 11:64869703 T CCDS8093.1 CCDS8093.1 Transcript intron_variant - - - - - - rs2844286 11:64869703 T ENSESTG00000026622 ENSESTT00000067032 Transcript downstream_gene_variant - - - - - - DISTANCE=4625 rs2844286 11:64869703 T 738 NM_013265.2 Transcript intron_variant - - - - - - rs2844286 11:64869703 T ENSESTG00000026622 ENSESTT00000067194 Transcript intron_variant - - - - - - rs7949780 11:64881608 A CCDS8094.1 CCDS8094.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2306 rs7949780 11:64881608 A 7108 NM_003273.2 Transcript intron_variant - - - - - - rs7949780 11:64881608 A ENSESTG00000026711 ENSESTT00000067349 Transcript intron_variant - - - - - - rs7949780 11:64881608 A ENSESTG00000026699 ENSESTT00000067230 Transcript downstream_gene_variant - - - - - - DISTANCE=2428 rs7949780 11:64881608 A CCDS41669.1 CCDS41669.1 Transcript intron_variant - - - - - - rs7949780 11:64881608 A ENSESTG00000026622 ENSESTT00000067194 Transcript downstream_gene_variant - - - - - - DISTANCE=3610 rs7949780 11:64881608 A ENSESTG00000026711 ENSESTT00000067375 Transcript upstream_gene_variant - - - - - - DISTANCE=1364 rs7949780 11:64881608 A CCDS8093.1 CCDS8093.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2549 rs7949780 11:64881608 A 741 NM_014205.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2267 rs7949780 11:64881608 A ENSESTG00000026711 ENSESTT00000067309 Transcript intron_variant - - - - - - rs7949780 11:64881608 A 738 NM_013265.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2428 rs7949780 11:64881608 A ENSESTG00000026711 ENSESTT00000067278 Transcript intron_variant - - - - - - rs1196041 11:64891363 G CCDS8095.1 CCDS8095.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2078 rs1196041 11:64891363 G 740 NM_004927.3 Transcript intron_variant - - - - - - rs1196041 11:64891363 G 2197 NM_001997.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1691 rs1196041 11:64891363 G 740 NR_037568.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1196041 11:64891363 G CCDS31605.1 CCDS31605.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4491 rs1196041 11:64891363 G 740 NR_037567.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1196041 11:64891363 G ENSESTG00000026827 ENSESTT00000067608 Transcript intron_variant - - - - - - rs1196041 11:64891363 G 84447 NM_172230.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3388 rs1196041 11:64891363 G ENSESTG00000028787 ENSESTT00000072518 Transcript downstream_gene_variant - - - - - - DISTANCE=4570 rs1196041 11:64891363 G 84447 NM_032431.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3388 rs1196041 11:64891363 G CCDS8096.1 CCDS8096.1 Transcript intron_variant - - - - - - rs1196041 11:64891363 G CCDS8097.1 CCDS8097.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4491 rs584972 11:65078334 C - ENSR00000563790 RegulatoryFeature regulatory_region_variant - - - - - - rs584972 11:65078334 C ENSESTG00000027402 ENSESTT00000069045 Transcript upstream_gene_variant - - - - - - DISTANCE=4003 rs584972 11:65078334 C 10435 NM_006779.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3955 rs7947140 11:65383896 C - ENSR00000563873 RegulatoryFeature regulatory_region_variant - - - - - - rs7947140 11:65383896 C ENSESTG00000027952 ENSESTT00000070377 Transcript upstream_gene_variant - - - - - - DISTANCE=2311 rs7947140 11:65383896 C ENSESTG00000028486 ENSESTT00000071602 Transcript upstream_gene_variant - - - - - - DISTANCE=2173 rs7947140 11:65383896 C ENSESTG00000027952 ENSESTT00000070402 Transcript upstream_gene_variant - - - - - - DISTANCE=2814 rs7947140 11:65383896 C ENSESTG00000027920 ENSESTT00000070326 Transcript upstream_gene_variant - - - - - - DISTANCE=479 rs7947140 11:65383896 C CCDS8107.1 CCDS8107.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2669 rs7947140 11:65383896 C 4296 NM_002419.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2176 rs7947140 11:65383896 C ENSESTG00000027952 ENSESTT00000070417 Transcript upstream_gene_variant - - - - - - DISTANCE=3111 rs7947140 11:65383896 C 399909 NM_032223.2 Transcript synonymous_variant 114 114 38 V gtG/gtC - rs7947140 11:65383896 C ENSESTG00000028480 ENSESTT00000071581 Transcript intron_variant - - - - - - rs7947140 11:65383896 C CCDS44650.1 CCDS44650.1 Transcript synonymous_variant 114 114 38 V gtG/gtC - rs7947140 11:65383896 C ENSESTG00000028495 ENSESTT00000071622 Transcript upstream_gene_variant - - - - - - DISTANCE=2963 rs7947140 11:65383896 C ENSESTG00000027920 ENSESTT00000070308 Transcript 5_prime_UTR_variant 11 - - - - - rs616250 11:65480596 G ENSESTG00000028340 ENSESTT00000071296 Transcript downstream_gene_variant - - - - - - DISTANCE=1874 rs616250 11:65480596 G 10524 NM_001206833.1 Transcript intron_variant - - - - - - rs616250 11:65480596 G ENSESTG00000028216 ENSESTT00000070969 Transcript downstream_gene_variant - - - - - - DISTANCE=111 rs616250 11:65480596 G CCDS8109.1 CCDS8109.1 Transcript intron_variant - - - - - - rs616250 11:65480596 G ENSESTG00000028216 ENSESTT00000071147 Transcript upstream_gene_variant - - - - - - DISTANCE=3108 rs616250 11:65480596 G 84153 NM_032193.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4548 rs616250 11:65480596 G ENSESTG00000028216 ENSESTT00000071115 Transcript intron_variant - - - - - - rs616250 11:65480596 G 10524 NM_006388.3 Transcript intron_variant - - - - - - rs616250 11:65480596 G ENSESTG00000028216 ENSESTT00000070944 Transcript downstream_gene_variant - - - - - - DISTANCE=166 rs616250 11:65480596 G 10524 NM_182709.2 Transcript intron_variant - - - - - - rs616250 11:65480596 G CCDS55771.1 CCDS55771.1 Transcript intron_variant - - - - - - rs616250 11:65480596 G 10524 NM_182710.2 Transcript intron_variant - - - - - - rs616250 11:65480596 G ENSESTG00000028216 ENSESTT00000071129 Transcript upstream_gene_variant - - - - - - DISTANCE=1695 rs616250 11:65480596 G CCDS8110.1 CCDS8110.1 Transcript intron_variant - - - - - - rs616250 11:65480596 G ENSESTG00000028216 ENSESTT00000071089 Transcript intron_variant - - - - - - rs616250 11:65480596 G CCDS31610.1 CCDS31610.1 Transcript intron_variant - - - - - - rs616250 11:65480596 G ENSESTG00000028371 ENSESTT00000071326 Transcript downstream_gene_variant - - - - - - DISTANCE=1371 rs10750770 11:65549906 C ENSESTG00000015811 ENSESTT00000039643 Transcript upstream_gene_variant - - - - - - DISTANCE=4630 rs10750770 11:65549906 C CCDS8112.1 CCDS8112.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4939 rs10750770 11:65549906 C 5017 NM_004561.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4599 rs10750770 11:65549906 C ENSESTG00000015805 ENSESTT00000039601 Transcript downstream_gene_variant - - - - - - DISTANCE=2165 rs10750770 11:65549906 C CCDS58146.1 CCDS58146.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1844 rs10750770 11:65549906 C 91056 NM_138368.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1844 rs9735836 11:65711710 T 254187 NM_152762.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1405 rs9735836 11:65711710 T ENSESTG00000015983 ENSESTT00000040088 Transcript upstream_gene_variant - - - - - - DISTANCE=1452 rs9735836 11:65711710 T ENSESTG00000015983 ENSESTT00000040085 Transcript upstream_gene_variant - - - - - - DISTANCE=1206 rs9667471 11:65806301 C CCDS8128.1 CCDS8128.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3677 rs9667471 11:65806301 C 89792 NM_033036.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1935 rs559671 11:66602673 A - ENSR00001051615 RegulatoryFeature regulatory_region_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039071 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039036 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000038964 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039003 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039075 Transcript upstream_gene_variant - - - - - - DISTANCE=3163 rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039057 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039029 Transcript intron_variant - - - - - - rs559671 11:66602673 A 79703 NR_048553.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039002 Transcript intron_variant - - - - - - rs559671 11:66602673 A CCDS53664.1 CCDS53664.1 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039032 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000038961 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039040 Transcript intron_variant - - - - - - rs559671 11:66602673 A 79703 NM_024650.3 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039065 Transcript intron_variant - - - - - - rs559671 11:66602673 A ENSESTG00000015515 ENSESTT00000039060 Transcript intron_variant - - - - - - rs4930397 11:66706842 T ENSESTG00000016822 ENSESTT00000042384 Transcript intron_variant - - - - - - rs4930397 11:66706842 T ENSESTG00000016822 ENSESTT00000042397 Transcript intron_variant - - - - - - rs4930397 11:66706842 T 5091 NM_001040716.1 Transcript intron_variant - - - - - - rs4930397 11:66706842 T 100423029 NR_036121.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4865 rs4930397 11:66706842 T 5091 NM_000920.3 Transcript intron_variant - - - - - - rs4930397 11:66706842 T ENSESTG00000016822 ENSESTT00000042348 Transcript intron_variant - - - - - - rs4930397 11:66706842 T ENSESTG00000016822 ENSESTT00000042364 Transcript intron_variant - - - - - - rs4930397 11:66706842 T ENSESTG00000016822 ENSESTT00000042354 Transcript intron_variant - - - - - - rs4930409 11:66837965 C CCDS8155.1 CCDS8155.1 Transcript missense_variant 400 400 134 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs4930409 11:66837965 C 29984 NM_014578.3 Transcript missense_variant 485 400 134 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs4930409 11:66837965 C ENSESTG00000015676 ENSESTT00000039248 Transcript missense_variant 621 310 104 C/R Tgc/Cgc - rs4930409 11:66837965 C ENSESTG00000015676 ENSESTT00000039268 Transcript missense_variant 485 400 134 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs4930199 11:67258391 G CCDS31620.1 CCDS31620.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1113 rs4930199 11:67258391 G 9049 NM_003977.2 Transcript missense_variant 1045 920 307 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs4930199 11:67258391 G CCDS8168.1 CCDS8168.1 Transcript missense_variant 920 920 307 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs4930199 11:67258391 G 9600 NM_001130848.1 Transcript downstream_gene_variant - - - - - - DISTANCE=848 rs4930199 11:67258391 G ENSESTG00000016465 ENSESTT00000041493 Transcript downstream_gene_variant - - - - - - DISTANCE=2864 rs4930199 11:67258391 G ENSESTG00000016211 ENSESTT00000040731 Transcript downstream_gene_variant - - - - - - DISTANCE=695 rs4930199 11:67258391 G 9600 NM_004910.2 Transcript downstream_gene_variant - - - - - - DISTANCE=848 rs4930199 11:67258391 G ENSESTG00000016465 ENSESTT00000041510 Transcript downstream_gene_variant - - - - - - DISTANCE=849 rs4930199 11:67258391 G ENSESTG00000016211 ENSESTT00000040696 Transcript downstream_gene_variant - - - - - - DISTANCE=846 rs4930199 11:67258391 G CCDS44659.1 CCDS44659.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1113 rs4930199 11:67258391 G ENSESTG00000016211 ENSESTT00000040748 Transcript downstream_gene_variant - - - - - - DISTANCE=10 rs4930199 11:67258391 G ENSESTG00000016465 ENSESTT00000041473 Transcript downstream_gene_variant - - - - - - DISTANCE=1286 rs3133487 11:67613664 G - - - intergenic_variant - - - - - - rs2512606 11:67957518 T 51111 NM_016028.4 Transcript missense_variant 282 26 9 I/N aTc/aAc - PolyPhen=benign;SIFT=tolerated rs2512606 11:67957518 T ENSESTG00000017489 ENSESTT00000044046 Transcript missense_variant 245 26 9 I/N aTc/aAc - rs2512606 11:67957518 T CCDS31623.1 CCDS31623.1 Transcript missense_variant 26 26 9 I/N aTc/aAc - PolyPhen=benign;SIFT=tolerated rs2512606 11:67957518 T 51111 NM_017635.3 Transcript missense_variant 282 26 9 I/N aTc/aAc - PolyPhen=benign;SIFT=tolerated rs2512606 11:67957518 T CCDS44660.1 CCDS44660.1 Transcript missense_variant 26 26 9 I/N aTc/aAc - PolyPhen=benign;SIFT=tolerated rs2512606 11:67957518 T ENSESTG00000017489 ENSESTT00000044073 Transcript missense_variant 261 26 9 I/N aTc/aAc - rs2512606 11:67957518 T ENSESTG00000017489 ENSESTT00000044051 Transcript missense_variant 245 26 9 I/N aTc/aAc - rs2512607 11:67960826 T - ENSR00001570997 RegulatoryFeature regulatory_region_variant - - - - - - rs2512607 11:67960826 T 51111 NM_016028.4 Transcript intron_variant - - - - - - rs2512607 11:67960826 T ENSESTG00000017489 ENSESTT00000044046 Transcript intron_variant - - - - - - rs2512607 11:67960826 T CCDS31623.1 CCDS31623.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3283 rs2512607 11:67960826 T 51111 NM_017635.3 Transcript intron_variant - - - - - - rs2512607 11:67960826 T CCDS44660.1 CCDS44660.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3283 rs2512607 11:67960826 T ENSESTG00000017489 ENSESTT00000044073 Transcript intron_variant - - - - - - rs2512607 11:67960826 T ENSESTG00000017489 ENSESTT00000044051 Transcript intron_variant - - - - - - rs624210 11:68037314 T - ENSR00001570999 RegulatoryFeature regulatory_region_variant - - - - - - rs624210 11:68037314 T ENSESTG00000017376 ENSESTT00000043801 Transcript intron_variant - - - - - - rs624210 11:68037314 T ENSESTG00000017376 ENSESTT00000043779 Transcript intron_variant - - - - - - rs624210 11:68037314 T 53838 NM_022338.3 Transcript intron_variant - - - - - - rs537279 11:68072289 C - - - intergenic_variant - - - - - - rs678765 11:68107827 G - ENSR00000685689 RegulatoryFeature regulatory_region_variant - - - - - - rs678765 11:68107827 G CCDS8181.1 CCDS8181.1 Transcript intron_variant - - - - - - rs678765 11:68107827 G 4041 NM_002335.2 Transcript intron_variant - - - - - - rs10791978 11:68131167 T CCDS8181.1 CCDS8181.1 Transcript intron_variant - - - - - - rs10791978 11:68131167 T ENSESTG00000017018 ENSESTT00000042749 Transcript intron_variant - - - - - - rs10791978 11:68131167 T 4041 NM_002335.2 Transcript intron_variant - - - - - - rs618340 11:68149755 A CCDS8181.1 CCDS8181.1 Transcript intron_variant - - - - - - rs618340 11:68149755 A ENSESTG00000017018 ENSESTT00000042749 Transcript intron_variant - - - - - - rs618340 11:68149755 A 4041 NM_002335.2 Transcript intron_variant - - - - - - rs618340 11:68149755 A ENSESTG00000017031 ENSESTT00000042814 Transcript upstream_gene_variant - - - - - - DISTANCE=4324 rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043411 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043375 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043465 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043323 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043123 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043368 Transcript intron_variant - - - - - - rs1941057 11:68304791 C 55291 NM_001164163.1 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043250 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043332 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043475 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043472 Transcript intron_variant - - - - - - rs1941057 11:68304791 C 55291 NM_018312.4 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043446 Transcript intron_variant - - - - - - rs1941057 11:68304791 C CCDS53673.1 CCDS53673.1 Transcript upstream_gene_variant - - - - - - DISTANCE=342 rs1941057 11:68304791 C CCDS53675.1 CCDS53675.1 Transcript upstream_gene_variant - - - - - - DISTANCE=342 rs1941057 11:68304791 C 55291 NM_001164161.1 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043344 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043398 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043480 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043354 Transcript intron_variant - - - - - - rs1941057 11:68304791 C 55291 NM_001164164.1 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043306 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043440 Transcript intron_variant - - - - - - rs1941057 11:68304791 C CCDS53674.1 CCDS53674.1 Transcript upstream_gene_variant - - - - - - DISTANCE=342 rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043381 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043456 Transcript intron_variant - - - - - - rs1941057 11:68304791 C CCDS53672.1 CCDS53672.1 Transcript upstream_gene_variant - - - - - - DISTANCE=342 rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043393 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043261 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043422 Transcript intron_variant - - - - - - rs1941057 11:68304791 C 55291 NM_001164162.1 Transcript intron_variant - - - - - - rs1941057 11:68304791 C ENSESTG00000017166 ENSESTT00000043415 Transcript intron_variant - - - - - - rs1941057 11:68304791 C CCDS53671.1 CCDS53671.1 Transcript upstream_gene_variant - - - - - - DISTANCE=342 rs1941057 11:68304791 C CCDS8182.1 CCDS8182.1 Transcript upstream_gene_variant - - - - - - DISTANCE=342 rs1941057 11:68304791 C 55291 NM_001164160.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043411 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043375 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043465 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043323 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043368 Transcript intron_variant - - - - - - rs10791983 11:68346483 T 55291 NM_001164163.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043250 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043576 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043332 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043529 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043522 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043472 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043496 Transcript intron_variant - - - - - - rs10791983 11:68346483 T 55291 NM_018312.4 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043446 Transcript intron_variant - - - - - - rs10791983 11:68346483 T CCDS53673.1 CCDS53673.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T CCDS53675.1 CCDS53675.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T 55291 NM_001164161.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043344 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043398 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043540 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043503 Transcript intron_variant - - - - - - rs10791983 11:68346483 T 55291 NM_001164164.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043306 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043440 Transcript intron_variant - - - - - - rs10791983 11:68346483 T CCDS53674.1 CCDS53674.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043381 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043568 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043456 Transcript intron_variant - - - - - - rs10791983 11:68346483 T CCDS53672.1 CCDS53672.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043562 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043393 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043533 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043261 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043422 Transcript intron_variant - - - - - - rs10791983 11:68346483 T 55291 NM_001164162.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T CCDS53671.1 CCDS53671.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T CCDS8182.1 CCDS8182.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T 55291 NM_001164160.1 Transcript intron_variant - - - - - - rs10791983 11:68346483 T ENSESTG00000017166 ENSESTT00000043581 Transcript upstream_gene_variant - - - - - - DISTANCE=4027 rs2510378 11:68436127 G - - - intergenic_variant - - - - - - rs3019599 11:68561335 C - ENSR00001052516 RegulatoryFeature regulatory_region_variant - - - - - - rs3019599 11:68561335 C ENSESTG00000034129 ENSESTT00000086312 Transcript intron_variant - - - - - - rs3019599 11:68561335 C ENSESTG00000034129 ENSESTT00000086266 Transcript downstream_gene_variant - - - - - - DISTANCE=3023 rs3019599 11:68561335 C ENSESTG00000034129 ENSESTT00000086282 Transcript downstream_gene_variant - - - - - - DISTANCE=3023 rs3019599 11:68561335 C CCDS8185.1 CCDS8185.1 Transcript intron_variant - - - - - - rs3019599 11:68561335 C 1374 NM_001031847.2 Transcript intron_variant - - - - - - rs3019599 11:68561335 C CCDS31624.1 CCDS31624.1 Transcript intron_variant - - - - - - rs3019599 11:68561335 C 1374 NM_001876.3 Transcript intron_variant - - - - - - rs3019599 11:68561335 C ENSESTG00000034129 ENSESTT00000086314 Transcript intron_variant - - - - - - rs4930611 11:68561908 T ENSESTG00000034129 ENSESTT00000086312 Transcript intron_variant - - - - - - rs4930611 11:68561908 T ENSESTG00000034129 ENSESTT00000086266 Transcript downstream_gene_variant - - - - - - DISTANCE=2450 rs4930611 11:68561908 T ENSESTG00000034129 ENSESTT00000086282 Transcript downstream_gene_variant - - - - - - DISTANCE=2450 rs4930611 11:68561908 T CCDS8185.1 CCDS8185.1 Transcript intron_variant - - - - - - rs4930611 11:68561908 T 1374 NM_001031847.2 Transcript intron_variant - - - - - - rs4930611 11:68561908 T CCDS31624.1 CCDS31624.1 Transcript intron_variant - - - - - - rs4930611 11:68561908 T 1374 NM_001876.3 Transcript intron_variant - - - - - - rs4930611 11:68561908 T ENSESTG00000034129 ENSESTT00000086314 Transcript intron_variant - - - - - - rs3019745 11:68841687 G ENSESTG00000034004 ENSESTT00000086000 Transcript intron_variant - - - - - - rs3019745 11:68841687 G 219931 NM_139075.3 Transcript intron_variant - - - - - - rs3019745 11:68841687 G ENSESTG00000034004 ENSESTT00000085986 Transcript downstream_gene_variant - - - - - - DISTANCE=3748 rs3019745 11:68841687 G CCDS8189.1 CCDS8189.1 Transcript intron_variant - - - - - - rs2924535 11:68870397 C - ENSR00001571062 RegulatoryFeature regulatory_region_variant - - - - - - rs2924535 11:68870397 C ENSESTG00000034039 ENSESTT00000086032 Transcript upstream_gene_variant - - - - - - DISTANCE=564 rs1993255 11:68901537 C - - - intergenic_variant - - - - - - rs61882194 11:69197514 A - ENSR00001571090 RegulatoryFeature regulatory_region_variant - - - - - - rs61882194 11:69197514 A - - - intergenic_variant - - - - - - rs2510605 11:69493485 T CCDS8192.1 CCDS8192.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3478 rs2510605 11:69493485 T 220064 NM_153451.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3320 rs2510605 11:69493485 T ENSESTG00000034069 ENSESTT00000086148 Transcript upstream_gene_variant - - - - - - DISTANCE=3412 rs2510605 11:69493485 T ENSESTG00000034069 ENSESTT00000086145 Transcript upstream_gene_variant - - - - - - DISTANCE=3393 rs6606658 11:69537919 C - - - intergenic_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085138 Transcript intron_variant - - - - - - rs10751231 11:70208350 A 8500 NM_177423.2 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085232 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085131 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085116 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085053 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085182 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085156 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085240 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085177 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085081 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085068 Transcript intron_variant - - - - - - rs10751231 11:70208350 A 8500 NR_045286.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085224 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085113 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085234 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085172 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085188 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085215 Transcript intron_variant - - - - - - rs10751231 11:70208350 A CCDS31627.1 CCDS31627.1 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085101 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085162 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085158 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085238 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085107 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085159 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085223 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085192 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085128 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085079 Transcript intron_variant - - - - - - rs10751231 11:70208350 A CCDS31628.1 CCDS31628.1 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085217 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085198 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085124 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085168 Transcript intron_variant - - - - - - rs10751231 11:70208350 A 8500 NM_003626.3 Transcript intron_variant - - - - - - rs10751231 11:70208350 A ENSESTG00000033613 ENSESTT00000085202 Transcript intron_variant - - - - - - rs7931294 11:70624143 G ENSESTG00000005872 ENSESTT00000014915 Transcript intron_variant - - - - - - rs7931294 11:70624143 G ENSESTG00000005872 ENSESTT00000014899 Transcript intron_variant - - - - - - rs7931294 11:70624143 G 22941 NM_012309.3 Transcript intron_variant - - - - - - rs7931294 11:70624143 G ENSESTG00000005872 ENSESTT00000014907 Transcript intron_variant - - - - - - rs3017481 11:70714468 G ENSESTG00000005872 ENSESTT00000014899 Transcript intron_variant - - - - - - rs3017481 11:70714468 G 100500844 NR_037437.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3907 rs3017481 11:70714468 G 22941 NM_012309.3 Transcript intron_variant - - - - - - rs3017481 11:70714468 G ENSESTG00000005872 ENSESTT00000014907 Transcript intron_variant - - - - - - rs636618 11:70720440 C ENSESTG00000005872 ENSESTT00000014899 Transcript upstream_gene_variant - - - - - - DISTANCE=1213 rs636618 11:70720440 C 100500844 NR_037437.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1967 rs636618 11:70720440 C 22941 NM_012309.3 Transcript intron_variant - - - - - - rs636618 11:70720440 C ENSESTG00000005872 ENSESTT00000014907 Transcript upstream_gene_variant - - - - - - DISTANCE=1213 rs542235 11:70721240 G ENSESTG00000005872 ENSESTT00000014899 Transcript upstream_gene_variant - - - - - - DISTANCE=2013 rs542235 11:70721240 G 100500844 NR_037437.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2767 rs542235 11:70721240 G 22941 NM_012309.3 Transcript intron_variant - - - - - - rs542235 11:70721240 G ENSESTG00000005872 ENSESTT00000014907 Transcript upstream_gene_variant - - - - - - DISTANCE=2013 rs7480292 11:70767380 C 22941 NM_012309.3 Transcript intron_variant - - - - - - rs10751015 11:70812047 G ENSESTG00000005863 ENSESTT00000014874 Transcript intron_variant - - - - - - rs10751015 11:70812047 G 22941 NM_012309.3 Transcript intron_variant - - - - - - rs3020033 11:70961132 G - - - intergenic_variant - - - - - - rs3133260 11:71040179 T - ENSR00000685773 RegulatoryFeature regulatory_region_variant - - - - - - rs3133260 11:71040179 T - - - intergenic_variant - - - - - - rs1660869 11:71073212 G - ENSR00000685775 RegulatoryFeature regulatory_region_variant - - - - - - rs1660869 11:71073212 G - - - intergenic_variant - - - - - - rs1792223 11:71153757 C ENSESTG00000005838 ENSESTT00000014834 Transcript intron_variant - - - - - - rs1792223 11:71153757 C ENSESTG00000005838 ENSESTT00000014822 Transcript intron_variant - - - - - - rs1792223 11:71153757 C ENSESTG00000005838 ENSESTT00000014839 Transcript intron_variant - - - - - - rs1792223 11:71153757 C CCDS8200.1 CCDS8200.1 Transcript intron_variant - - - - - - rs1792223 11:71153757 C 1717 NM_001163817.1 Transcript intron_variant - - - - - - rs1792223 11:71153757 C 1717 NM_001360.2 Transcript intron_variant - - - - - - rs4414250 11:71194536 C ENSESTG00000005795 ENSESTT00000014714 Transcript intron_variant - - - - - - rs4414250 11:71194536 C CCDS8201.1 CCDS8201.1 Transcript intron_variant - - - - - - rs4414250 11:71194536 C ENSESTG00000005795 ENSESTT00000014720 Transcript intron_variant - - - - - - rs4414250 11:71194536 C ENSESTG00000005795 ENSESTT00000014731 Transcript downstream_gene_variant - - - - - - DISTANCE=4408 rs4414250 11:71194536 C 55191 NM_018161.4 Transcript intron_variant - - - - - - rs2508202 11:71932120 C ENSESTG00000006995 ENSESTT00000017720 Transcript upstream_gene_variant - - - - - - DISTANCE=2689 rs2508202 11:71932120 C 2350 NM_001113534.1 Transcript intron_variant - - - - - - rs2508202 11:71932120 C 2350 NM_001113536.1 Transcript intron_variant - - - - - - rs2508202 11:71932120 C 2350 NM_001113535.1 Transcript intron_variant - - - - - - rs2508202 11:71932120 C ENSESTG00000006999 ENSESTT00000017727 Transcript upstream_gene_variant - - - - - - DISTANCE=3993 rs2508202 11:71932120 C CCDS8213.1 CCDS8213.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3909 rs2508202 11:71932120 C 2350 NM_000803.4 Transcript intron_variant - - - - - - rs2508202 11:71932120 C 3636 NM_001567.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3762 rs2508202 11:71932120 C CCDS8212.1 CCDS8212.1 Transcript intron_variant - - - - - - rs2508202 11:71932120 C ENSESTG00000006983 ENSESTT00000017712 Transcript intron_variant - - - - - - rs2508202 11:71932120 C ENSESTG00000006981 ENSESTT00000017684 Transcript downstream_gene_variant - - - - - - DISTANCE=2372 rs10751202 11:72097479 T ENSESTG00000007284 ENSESTT00000018426 Transcript intron_variant - - - - - - rs10751202 11:72097479 T 81570 NM_001258393.1 Transcript intron_variant - - - - - - rs10751202 11:72097479 T 81570 NM_030813.4 Transcript intron_variant - - - - - - rs10751202 11:72097479 T CCDS58153.1 CCDS58153.1 Transcript intron_variant - - - - - - rs10751202 11:72097479 T CCDS58152.1 CCDS58152.1 Transcript intron_variant - - - - - - rs10751202 11:72097479 T CCDS8215.1 CCDS8215.1 Transcript intron_variant - - - - - - rs10751202 11:72097479 T 81570 NM_001258392.1 Transcript intron_variant - - - - - - rs10751202 11:72097479 T ENSESTG00000007284 ENSESTT00000018441 Transcript intron_variant - - - - - - rs10751202 11:72097479 T 81570 NM_001258394.1 Transcript intron_variant - - - - - - rs10751202 11:72097479 T CCDS58154.1 CCDS58154.1 Transcript intron_variant - - - - - - rs367829 11:72280543 T - - - intergenic_variant - - - - - - rs409512 11:72282039 C - ENSR00000565037 RegulatoryFeature regulatory_region_variant - - - - - - rs409512 11:72282039 C - - - intergenic_variant - - - - - - rs2449665 11:72494958 T ENSESTG00000014960 ENSESTT00000037460 Transcript intron_variant - - - - - - rs2449665 11:72494958 T CCDS41688.1 CCDS41688.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2732 rs2449665 11:72494958 T 10809 NM_006645.2 Transcript intron_variant - - - - - - rs2449665 11:72494958 T 100616410 NR_039841.1 Transcript downstream_gene_variant - - - - - - DISTANCE=321 rs4245436 11:72527324 C ENSESTG00000019651 ENSESTT00000049324 Transcript 3_prime_UTR_variant 393 - - - - - rs4245436 11:72527324 C 89849 NM_033388.1 Transcript intron_variant - - - - - - rs4245436 11:72527324 C CCDS31634.1 CCDS31634.1 Transcript intron_variant - - - - - - rs4245436 11:72527324 C ENSESTG00000019651 ENSESTT00000049314 Transcript intron_variant - - - - - - rs4245436 11:72527324 C ENSESTG00000019651 ENSESTT00000049307 Transcript intron_variant - - - - - - rs4245436 11:72527324 C ENSESTG00000019600 ENSESTT00000049181 Transcript upstream_gene_variant - - - - - - DISTANCE=4173 rs1864652 11:72532621 G - ENSR00000565093 RegulatoryFeature regulatory_region_variant - - - - - - rs1864652 11:72532621 G ENSESTG00000019651 ENSESTT00000049324 Transcript downstream_gene_variant - - - - - - DISTANCE=3795 rs1864652 11:72532621 G ENSESTG00000019600 ENSESTT00000049202 Transcript upstream_gene_variant - - - - - - DISTANCE=613 rs1864652 11:72532621 G ENSESTG00000019651 ENSESTT00000049314 Transcript downstream_gene_variant - - - - - - DISTANCE=174 rs1864652 11:72532621 G ENSESTG00000019651 ENSESTT00000049307 Transcript intron_variant - - - - - - rs1864652 11:72532621 G ENSESTG00000019600 ENSESTT00000049181 Transcript intron_variant - - - - - - rs1864652 11:72532621 G 89849 NM_033388.1 Transcript intron_variant - - - - - - rs1864652 11:72532621 G ENSESTG00000019600 ENSESTT00000049255 Transcript upstream_gene_variant - - - - - - DISTANCE=855 rs1864652 11:72532621 G CCDS31634.1 CCDS31634.1 Transcript intron_variant - - - - - - rs1864652 11:72532621 G ENSESTG00000019600 ENSESTT00000049245 Transcript upstream_gene_variant - - - - - - DISTANCE=747 rs7127601 11:72555247 G ENSESTG00000014909 ENSESTT00000037428 Transcript intron_variant - - - - - - rs7127601 11:72555247 G ENSESTG00000014909 ENSESTT00000037388 Transcript intron_variant - - - - - - rs7127601 11:72555247 G 9873 NM_014824.2 Transcript intron_variant - - - - - - rs7127601 11:72555247 G ENSESTG00000014909 ENSESTT00000037417 Transcript intron_variant - - - - - - rs7127601 11:72555247 G ENSESTG00000014909 ENSESTT00000037441 Transcript intron_variant - - - - - - rs7127601 11:72555247 G ENSESTG00000014909 ENSESTT00000037384 Transcript intron_variant - - - - - - rs7127601 11:72555247 G ENSESTG00000014909 ENSESTT00000037437 Transcript intron_variant - - - - - - rs7127601 11:72555247 G CCDS8218.2 CCDS8218.2 Transcript intron_variant - - - - - - rs7127601 11:72555247 G ENSESTG00000014909 ENSESTT00000037430 Transcript intron_variant - - - - - - rs10751218 11:72568211 G - ENSR00000565099 RegulatoryFeature regulatory_region_variant - - - - - - rs10751218 11:72568211 G ENSESTG00000014909 ENSESTT00000037428 Transcript intron_variant - - - - - - rs10751218 11:72568211 G ENSESTG00000014909 ENSESTT00000037388 Transcript intron_variant - - - - - - rs10751218 11:72568211 G 9873 NM_014824.2 Transcript intron_variant - - - - - - rs10751218 11:72568211 G ENSESTG00000014909 ENSESTT00000037417 Transcript intron_variant - - - - - - rs10751218 11:72568211 G ENSESTG00000014909 ENSESTT00000037441 Transcript intron_variant - - - - - - rs10751218 11:72568211 G ENSESTG00000014909 ENSESTT00000037384 Transcript intron_variant - - - - - - rs10751218 11:72568211 G ENSESTG00000014909 ENSESTT00000037437 Transcript intron_variant - - - - - - rs10751218 11:72568211 G CCDS8218.2 CCDS8218.2 Transcript intron_variant - - - - - - rs10751218 11:72568211 G ENSESTG00000014909 ENSESTT00000037430 Transcript intron_variant - - - - - - rs4944811 11:72577083 G ENSESTG00000014909 ENSESTT00000037428 Transcript intron_variant - - - - - - rs4944811 11:72577083 G ENSESTG00000014909 ENSESTT00000037388 Transcript intron_variant - - - - - - rs4944811 11:72577083 G 9873 NM_014824.2 Transcript intron_variant - - - - - - rs4944811 11:72577083 G ENSESTG00000014909 ENSESTT00000037417 Transcript intron_variant - - - - - - rs4944811 11:72577083 G ENSESTG00000014909 ENSESTT00000037441 Transcript intron_variant - - - - - - rs4944811 11:72577083 G ENSESTG00000014909 ENSESTT00000037384 Transcript intron_variant - - - - - - rs4944811 11:72577083 G ENSESTG00000014909 ENSESTT00000037437 Transcript intron_variant - - - - - - rs4944811 11:72577083 G CCDS8218.2 CCDS8218.2 Transcript intron_variant - - - - - - rs4944811 11:72577083 G ENSESTG00000014909 ENSESTT00000037430 Transcript intron_variant - - - - - - rs2060071 11:72643360 A - ENSR00001571384 RegulatoryFeature regulatory_region_variant - - - - - - rs2060071 11:72643360 A ENSESTG00000014909 ENSESTT00000037428 Transcript intron_variant - - - - - - rs2060071 11:72643360 A ENSESTG00000014909 ENSESTT00000037388 Transcript intron_variant - - - - - - rs2060071 11:72643360 A 9873 NM_014824.2 Transcript intron_variant - - - - - - rs2060071 11:72643360 A ENSESTG00000014909 ENSESTT00000037417 Transcript intron_variant - - - - - - rs2060071 11:72643360 A ENSESTG00000014909 ENSESTT00000037384 Transcript intron_variant - - - - - - rs2060071 11:72643360 A ENSESTG00000014909 ENSESTT00000037437 Transcript intron_variant - - - - - - rs2060071 11:72643360 A CCDS8218.2 CCDS8218.2 Transcript intron_variant - - - - - - rs2060071 11:72643360 A ENSESTG00000014909 ENSESTT00000037430 Transcript intron_variant - - - - - - rs7936863 11:72668730 G ENSESTG00000014909 ENSESTT00000037428 Transcript intron_variant - - - - - - rs7936863 11:72668730 G ENSESTG00000014909 ENSESTT00000037388 Transcript intron_variant - - - - - - rs7936863 11:72668730 G 9873 NM_014824.2 Transcript intron_variant - - - - - - rs7936863 11:72668730 G ENSESTG00000014909 ENSESTT00000037417 Transcript intron_variant - - - - - - rs7936863 11:72668730 G ENSESTG00000014909 ENSESTT00000037384 Transcript intron_variant - - - - - - rs7936863 11:72668730 G ENSESTG00000014909 ENSESTT00000037437 Transcript intron_variant - - - - - - rs7936863 11:72668730 G CCDS8218.2 CCDS8218.2 Transcript intron_variant - - - - - - rs7936863 11:72668730 G ENSESTG00000014909 ENSESTT00000037430 Transcript intron_variant - - - - - - rs7944277 11:72737375 T ENSESTG00000014909 ENSESTT00000037384 Transcript intron_variant - - - - - - rs7944277 11:72737375 T ENSESTG00000014909 ENSESTT00000037428 Transcript intron_variant - - - - - - rs7944277 11:72737375 T ENSESTG00000014909 ENSESTT00000037388 Transcript intron_variant - - - - - - rs7944277 11:72737375 T ENSESTG00000014909 ENSESTT00000037430 Transcript intron_variant - - - - - - rs7944277 11:72737375 T CCDS8218.2 CCDS8218.2 Transcript intron_variant - - - - - - rs7944277 11:72737375 T 9873 NM_014824.2 Transcript intron_variant - - - - - - rs7944277 11:72737375 T ENSESTG00000014909 ENSESTT00000037417 Transcript intron_variant - - - - - - rs2511243 11:72886305 C - - - intergenic_variant - - - - - - rs1791935 11:72898166 C - - - intergenic_variant - - - - - - rs1783592 11:72920052 A - - - intergenic_variant - - - - - - rs3108791 11:73244512 A ENSESTG00000020169 ENSESTT00000050615 Transcript intron_variant - - - - - - rs3108791 11:73244512 A ENSESTG00000020169 ENSESTT00000050631 Transcript intron_variant - - - - - - rs3108791 11:73244512 A 23201 NM_015159.1 Transcript intron_variant - - - - - - rs3108790 11:73244552 A ENSESTG00000020169 ENSESTT00000050615 Transcript intron_variant - - - - - - rs3108790 11:73244552 A ENSESTG00000020169 ENSESTT00000050631 Transcript intron_variant - - - - - - rs3108790 11:73244552 A 23201 NM_015159.1 Transcript intron_variant - - - - - - rs2464344 11:73244570 A ENSESTG00000020169 ENSESTT00000050615 Transcript intron_variant - - - - - - rs2464344 11:73244570 A ENSESTG00000020169 ENSESTT00000050631 Transcript intron_variant - - - - - - rs2464344 11:73244570 A 23201 NM_015159.1 Transcript intron_variant - - - - - - rs494522 11:73251306 T ENSESTG00000020169 ENSESTT00000050615 Transcript intron_variant - - - - - - rs494522 11:73251306 T ENSESTG00000020169 ENSESTT00000050631 Transcript intron_variant - - - - - - rs494522 11:73251306 T 23201 NM_015159.1 Transcript intron_variant - - - - - - rs675042 11:73700272 T - ENSR00000685833 RegulatoryFeature regulatory_region_variant - - - - - - rs675042 11:73700272 T - - - intergenic_variant - - - - - - rs3018186 11:73831307 T ENSESTG00000003915 ENSESTT00000009906 Transcript downstream_gene_variant - - - - - - DISTANCE=2816 rs3018186 11:73831307 T ENSESTG00000003934 ENSESTT00000009925 Transcript intron_variant - - - - - - rs3018186 11:73831307 T ENSESTG00000003915 ENSESTT00000009915 Transcript downstream_gene_variant - - - - - - DISTANCE=2816 rs3018186 11:73831307 T CCDS31636.1 CCDS31636.1 Transcript intron_variant - - - - - - rs3018186 11:73831307 T 26005 NM_015531.4 Transcript intron_variant - - - - - - rs7948057 11:73831455 G ENSESTG00000003915 ENSESTT00000009906 Transcript downstream_gene_variant - - - - - - DISTANCE=2668 rs7948057 11:73831455 G ENSESTG00000003934 ENSESTT00000009925 Transcript intron_variant - - - - - - rs7948057 11:73831455 G ENSESTG00000003915 ENSESTT00000009915 Transcript downstream_gene_variant - - - - - - DISTANCE=2668 rs7948057 11:73831455 G CCDS31636.1 CCDS31636.1 Transcript intron_variant - - - - - - rs7948057 11:73831455 G 26005 NM_015531.4 Transcript intron_variant - - - - - - rs547669 11:73969415 C CCDS44678.1 CCDS44678.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4860 rs547669 11:73969415 C ENSESTG00000003762 ENSESTT00000009542 Transcript downstream_gene_variant - - - - - - DISTANCE=3668 rs547669 11:73969415 C 51400 NM_016147.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3667 rs547669 11:73969415 C ENSESTG00000003762 ENSESTT00000009564 Transcript downstream_gene_variant - - - - - - DISTANCE=3668 rs904155 11:74109342 T - ENSR00000320317 RegulatoryFeature regulatory_region_variant - - - - - - rs904155 11:74109342 T ENSESTG00000003871 ENSESTT00000009754 Transcript 5_prime_UTR_variant 137 - - - - - rs904155 11:74109342 T CCDS8231.1 CCDS8231.1 Transcript upstream_gene_variant - - - - - - DISTANCE=136 rs904155 11:74109342 T 283209 NM_173582.3 Transcript 5_prime_UTR_variant 161 - - - - - rs904155 11:74109342 T 100616215 NR_039710.1 Transcript upstream_gene_variant - - - - - - DISTANCE=940 rs1540078 11:74403340 G 25884 NM_015424.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4134 rs1540078 11:74403340 G CCDS8234.1 CCDS8234.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4203 rs523068 11:74459340 G CCDS41691.1 CCDS41691.1 Transcript upstream_gene_variant - - - - - - DISTANCE=586 rs523068 11:74459340 G 254225 NM_001098638.1 Transcript upstream_gene_variant - - - - - - DISTANCE=573 rs1315287 11:74534499 G ENSESTG00000009058 ENSESTT00000022816 Transcript intron_variant - - - - - - rs1315287 11:74534499 G ENSESTG00000008761 ENSESTT00000021992 Transcript intron_variant - - - - - - rs1315287 11:74534499 G CCDS41691.1 CCDS41691.1 Transcript intron_variant - - - - - - rs1315287 11:74534499 G 254225 NM_001098638.1 Transcript intron_variant - - - - - - rs1282437 11:74564962 G CCDS58160.1 CCDS58160.1 Transcript intron_variant - - - - - - rs1282437 11:74564962 G 143570 NM_001270380.1 Transcript intron_variant - - - - - - rs1282437 11:74564962 G 143570 NM_001270381.1 Transcript intron_variant - - - - - - rs1282437 11:74564962 G CCDS44680.1 CCDS44680.1 Transcript intron_variant - - - - - - rs1282437 11:74564962 G CCDS58159.1 CCDS58159.1 Transcript intron_variant - - - - - - rs1282437 11:74564962 G ENSESTG00000009058 ENSESTT00000022809 Transcript intron_variant - - - - - - rs1282437 11:74564962 G ENSESTG00000009058 ENSESTT00000022813 Transcript intron_variant - - - - - - rs1282437 11:74564962 G ENSESTG00000009058 ENSESTT00000022801 Transcript intron_variant - - - - - - rs1282437 11:74564962 G 143570 NM_182969.2 Transcript intron_variant - - - - - - rs1621378 11:74904362 C 11309 NM_001145211.2 Transcript missense_variant 1265 1109 370 I/T aTc/aCc - PolyPhen=benign;SIFT=tolerated rs1621378 11:74904362 C CCDS8235.1 CCDS8235.1 Transcript missense_variant 1175 1175 392 I/T aTc/aCc - PolyPhen=benign;SIFT=tolerated rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022208 Transcript downstream_gene_variant - - - - - - DISTANCE=2 rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022194 Transcript downstream_gene_variant - - - - - - DISTANCE=2 rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022207 Transcript intron_variant - - - - - - rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022211 Transcript intron_variant - - - - - - rs1621378 11:74904362 C CCDS53679.1 CCDS53679.1 Transcript missense_variant 743 743 248 I/T aTc/aCc - PolyPhen=benign;SIFT=tolerated rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022203 Transcript downstream_gene_variant - - - - - - DISTANCE=2 rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022214 Transcript downstream_gene_variant - - - - - - DISTANCE=2 rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022178 Transcript downstream_gene_variant - - - - - - DISTANCE=2 rs1621378 11:74904362 C CCDS44683.1 CCDS44683.1 Transcript missense_variant 1109 1109 370 I/T aTc/aCc - PolyPhen=benign;SIFT=tolerated rs1621378 11:74904362 C ENSESTG00000008864 ENSESTT00000022238 Transcript upstream_gene_variant - - - - - - DISTANCE=180 rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022221 Transcript missense_variant 494 473 158 I/T aTc/aCc - rs1621378 11:74904362 C 11309 NM_001145212.2 Transcript missense_variant 1138 743 248 I/T aTc/aCc - PolyPhen=benign;SIFT=tolerated rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022198 Transcript downstream_gene_variant - - - - - - DISTANCE=2 rs1621378 11:74904362 C ENSESTG00000008864 ENSESTT00000022239 Transcript upstream_gene_variant - - - - - - DISTANCE=180 rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022148 Transcript downstream_gene_variant - - - - - - DISTANCE=2 rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022189 Transcript intron_variant - - - - - - rs1621378 11:74904362 C ENSESTG00000008817 ENSESTT00000022165 Transcript intron_variant - - - - - - rs1621378 11:74904362 C ENSESTG00000008864 ENSESTT00000022245 Transcript upstream_gene_variant - - - - - - DISTANCE=3142 rs1621378 11:74904362 C 11309 NM_007256.4 Transcript missense_variant 1570 1175 392 I/T aTc/aCc - PolyPhen=benign;SIFT=tolerated rs542276 11:75141958 T - ENSR00000565491 RegulatoryFeature regulatory_region_variant - - - - - - rs542276 11:75141958 T ENSESTG00000008874 ENSESTT00000022336 Transcript intron_variant - - - - - - rs542276 11:75141958 T 283212 NM_001039548.2 Transcript upstream_gene_variant - - - - - - DISTANCE=284 rs542276 11:75141958 T CCDS44685.2 CCDS44685.2 Transcript upstream_gene_variant - - - - - - DISTANCE=284 rs542276 11:75141958 T CCDS8238.1 CCDS8238.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4594 rs542276 11:75141958 T 81544 NM_030792.6 Transcript downstream_gene_variant - - - - - - DISTANCE=3727 rs1783558 11:75219235 G - ENSR00000189836 RegulatoryFeature regulatory_region_variant - - - - - - rs1783558 11:75219235 G ENSESTG00000008974 ENSESTT00000022546 Transcript intron_variant - - - - - - rs1783558 11:75219235 G ENSESTG00000008874 ENSESTT00000022336 Transcript intron_variant - - - - - - rs1783558 11:75219235 G ENSESTG00000008974 ENSESTT00000022540 Transcript intron_variant - - - - - - rs1783558 11:75219235 G 81544 NM_030792.6 Transcript intron_variant - - - - - - rs1974429 11:75253327 C ENSESTG00000008874 ENSESTT00000022336 Transcript downstream_gene_variant - - - - - - DISTANCE=1733 rs2508393 11:75472624 C ENSESTG00000035312 ENSESTT00000089189 Transcript intron_variant - - - - - - rs2508393 11:75472624 C ENSESTG00000035312 ENSESTT00000089182 Transcript intron_variant - - - - - - rs2508393 11:75472624 C 283214 NR_046090.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10899148 11:75650813 T ENSESTG00000035338 ENSESTT00000089271 Transcript intron_variant - - - - - - rs10899148 11:75650813 T ENSESTG00000035338 ENSESTT00000089252 Transcript intron_variant - - - - - - rs10899148 11:75650813 T 7405 NM_003369.3 Transcript intron_variant - - - - - - rs10899148 11:75650813 T CCDS8241.1 CCDS8241.1 Transcript intron_variant - - - - - - rs10899148 11:75650813 T ENSESTG00000035338 ENSESTT00000089264 Transcript intron_variant - - - - - - rs10899148 11:75650813 T ENSESTG00000035338 ENSESTT00000089261 Transcript intron_variant - - - - - - rs579075 11:75709800 A ENSESTG00000035338 ENSESTT00000089275 Transcript intron_variant - - - - - - rs579075 11:75709800 A ENSESTG00000035338 ENSESTT00000089277 Transcript intron_variant - - - - - - rs579075 11:75709800 A ENSESTG00000035338 ENSESTT00000089271 Transcript intron_variant - - - - - - rs579075 11:75709800 A ENSESTG00000035338 ENSESTT00000089252 Transcript intron_variant - - - - - - rs579075 11:75709800 A 7405 NM_003369.3 Transcript intron_variant - - - - - - rs579075 11:75709800 A CCDS8241.1 CCDS8241.1 Transcript intron_variant - - - - - - rs579075 11:75709800 A ENSESTG00000035338 ENSESTT00000089261 Transcript intron_variant - - - - - - rs7936482 11:76319266 G - - - intergenic_variant - - - - - - rs4304809 11:76370792 G ENSESTG00000035390 ENSESTT00000089353 Transcript downstream_gene_variant - - - - - - DISTANCE=1287 rs4304809 11:76370792 G ENSESTG00000035390 ENSESTT00000089355 Transcript downstream_gene_variant - - - - - - DISTANCE=1490 rs4304809 11:76370792 G 2615 NM_001128922.1 Transcript synonymous_variant 1983 1845 615 P ccT/ccC - rs4304809 11:76370792 G CCDS8245.1 CCDS8245.1 Transcript synonymous_variant 1845 1845 615 P ccT/ccC - rs4304809 11:76370792 G 2615 NM_005512.2 Transcript synonymous_variant 2088 1845 615 P ccT/ccC - rs6592658 11:76390574 C 390226 NR_024042.1 Transcript downstream_gene_variant - - - - - - DISTANCE=636 rs2451904 11:76486604 T - - - intergenic_variant - - - - - - rs3133368 11:76580452 A ENSESTG00000007918 ENSESTT00000019990 Transcript intron_variant - - - - - - rs3133368 11:76580452 A 55331 NM_018367.5 Transcript intron_variant - - - - - - rs3133368 11:76580452 A CCDS8247.1 CCDS8247.1 Transcript intron_variant - - - - - - rs3133368 11:76580452 A ENSESTG00000007918 ENSESTT00000020018 Transcript intron_variant - - - - - - rs3133368 11:76580452 A ENSESTG00000007918 ENSESTT00000020002 Transcript intron_variant - - - - - - rs594732 11:76600220 A - ENSR00000565753 RegulatoryFeature regulatory_region_variant - - - - - - rs594732 11:76600220 A ENSESTG00000007918 ENSESTT00000019990 Transcript intron_variant - - - - - - rs594732 11:76600220 A 55331 NM_018367.5 Transcript intron_variant - - - - - - rs594732 11:76600220 A CCDS8247.1 CCDS8247.1 Transcript intron_variant - - - - - - rs594732 11:76600220 A ENSESTG00000007918 ENSESTT00000020018 Transcript intron_variant - - - - - - rs594732 11:76600220 A ENSESTG00000007918 ENSESTT00000020002 Transcript intron_variant - - - - - - rs10736813 11:76877491 C ENSESTG00000008006 ENSESTT00000020234 Transcript downstream_gene_variant - - - - - - DISTANCE=3509 rs10736813 11:76877491 C 4647 NM_001127179.2 Transcript intron_variant - - - - - - rs10736813 11:76877491 C CCDS53685.1 CCDS53685.1 Transcript intron_variant - - - - - - rs10736813 11:76877491 C 4647 NM_001127180.1 Transcript intron_variant - - - - - - rs10736813 11:76877491 C CCDS53684.1 CCDS53684.1 Transcript intron_variant - - - - - - rs10736813 11:76877491 C CCDS53683.1 CCDS53683.1 Transcript intron_variant - - - - - - rs10736813 11:76877491 C 4647 NM_000260.3 Transcript intron_variant - - - - - - rs6592718 11:77076345 A CCDS8250.1 CCDS8250.1 Transcript intron_variant - - - - - - rs6592718 11:77076345 A CCDS44687.1 CCDS44687.1 Transcript intron_variant - - - - - - rs6592718 11:77076345 A ENSESTG00000008116 ENSESTT00000020526 Transcript intron_variant - - - - - - rs6592718 11:77076345 A 5058 NM_001128620.1 Transcript intron_variant - - - - - - rs6592718 11:77076345 A 5058 NM_002576.4 Transcript intron_variant - - - - - - rs1670440 11:77104255 T CCDS44687.1 CCDS44687.1 Transcript upstream_gene_variant - - - - - - DISTANCE=690 rs1670440 11:77104255 T ENSESTG00000008116 ENSESTT00000020533 Transcript intron_variant - - - - - - rs1670440 11:77104255 T 5058 NM_002576.4 Transcript intron_variant - - - - - - rs1670440 11:77104255 T ENSESTG00000008116 ENSESTT00000020543 Transcript intron_variant - - - - - - rs1670440 11:77104255 T ENSESTG00000008116 ENSESTT00000020520 Transcript intron_variant - - - - - - rs1670440 11:77104255 T ENSESTG00000008116 ENSESTT00000020538 Transcript intron_variant - - - - - - rs1670440 11:77104255 T CCDS8250.1 CCDS8250.1 Transcript upstream_gene_variant - - - - - - DISTANCE=690 rs1670440 11:77104255 T ENSESTG00000008116 ENSESTT00000020512 Transcript intron_variant - - - - - - rs1670440 11:77104255 T 5058 NM_001128620.1 Transcript intron_variant - - - - - - rs1670440 11:77104255 T ENSESTG00000008116 ENSESTT00000020526 Transcript intron_variant - - - - - - rs1670440 11:77104255 T ENSESTG00000008116 ENSESTT00000020531 Transcript intron_variant - - - - - - rs2466807 11:77105514 T CCDS44687.1 CCDS44687.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1949 rs2466807 11:77105514 T ENSESTG00000008116 ENSESTT00000020533 Transcript intron_variant - - - - - - rs2466807 11:77105514 T 5058 NM_002576.4 Transcript intron_variant - - - - - - rs2466807 11:77105514 T ENSESTG00000008116 ENSESTT00000020543 Transcript intron_variant - - - - - - rs2466807 11:77105514 T ENSESTG00000008116 ENSESTT00000020520 Transcript intron_variant - - - - - - rs2466807 11:77105514 T ENSESTG00000008116 ENSESTT00000020538 Transcript intron_variant - - - - - - rs2466807 11:77105514 T CCDS8250.1 CCDS8250.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1949 rs2466807 11:77105514 T ENSESTG00000008116 ENSESTT00000020512 Transcript intron_variant - - - - - - rs2466807 11:77105514 T 5058 NM_001128620.1 Transcript intron_variant - - - - - - rs2466807 11:77105514 T ENSESTG00000008116 ENSESTT00000020526 Transcript intron_variant - - - - - - rs2466807 11:77105514 T ENSESTG00000008116 ENSESTT00000020531 Transcript intron_variant - - - - - - rs480873 11:77146029 A ENSESTG00000008116 ENSESTT00000020520 Transcript intron_variant - - - - - - rs480873 11:77146029 A ENSESTG00000008116 ENSESTT00000020512 Transcript intron_variant - - - - - - rs480873 11:77146029 A ENSESTG00000008116 ENSESTT00000020526 Transcript intron_variant - - - - - - rs480873 11:77146029 A 5058 NM_001128620.1 Transcript intron_variant - - - - - - rs480873 11:77146029 A 5058 NM_002576.4 Transcript intron_variant - - - - - - rs1790247 11:77554574 A 28971 NM_024684.2 Transcript intron_variant - - - - - - rs1790247 11:77554574 A CCDS8254.1 CCDS8254.1 Transcript intron_variant - - - - - - rs1790247 11:77554574 A ENSESTG00000009366 ENSESTT00000023480 Transcript intron_variant - - - - - - rs3016159 11:77561960 T 28971 NM_024684.2 Transcript intron_variant - - - - - - rs3016159 11:77561960 T CCDS8254.1 CCDS8254.1 Transcript intron_variant - - - - - - rs3016159 11:77561960 T ENSESTG00000009366 ENSESTT00000023480 Transcript intron_variant - - - - - - rs648034 11:77771237 G 100532726 NM_001203262.1 Transcript intron_variant - - - - - - rs648034 11:77771237 G ENSESTG00000009556 ENSESTT00000024005 Transcript intron_variant - - - - - - rs648034 11:77771237 G CCDS8256.1 CCDS8256.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3691 rs648034 11:77771237 G 7069 NM_003251.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3670 rs648034 11:77771237 G 100532726 NM_001203261.1 Transcript intron_variant - - - - - - rs648034 11:77771237 G ENSESTG00000009556 ENSESTT00000024032 Transcript intron_variant - - - - - - rs648034 11:77771237 G 100532726 NM_001203260.1 Transcript intron_variant - - - - - - rs648034 11:77771237 G CCDS55780.1 CCDS55780.1 Transcript intron_variant - - - - - - rs648034 11:77771237 G ENSESTG00000009387 ENSESTT00000023523 Transcript upstream_gene_variant - - - - - - DISTANCE=3682 rs623365 11:77790142 A 100532726 NM_001203262.1 Transcript intron_variant - - - - - - rs623365 11:77790142 A 4718 NM_001204054.1 Transcript intron_variant - - - - - - rs623365 11:77790142 A ENSESTG00000009556 ENSESTT00000024005 Transcript intron_variant - - - - - - rs623365 11:77790142 A CCDS55781.1 CCDS55781.1 Transcript intron_variant - - - - - - rs623365 11:77790142 A ENSESTG00000009556 ENSESTT00000024025 Transcript intron_variant - - - - - - rs623365 11:77790142 A CCDS8257.1 CCDS8257.1 Transcript intron_variant - - - - - - rs623365 11:77790142 A 4718 NM_004549.5 Transcript intron_variant - - - - - - rs623365 11:77790142 A 100532726 NM_001203261.1 Transcript intron_variant - - - - - - rs623365 11:77790142 A 4718 NM_001204055.1 Transcript intron_variant - - - - - - rs623365 11:77790142 A ENSESTG00000009556 ENSESTT00000024032 Transcript intron_variant - - - - - - rs623365 11:77790142 A 100532726 NM_001203260.1 Transcript intron_variant - - - - - - rs623365 11:77790142 A CCDS55779.1 CCDS55779.1 Transcript intron_variant - - - - - - rs623365 11:77790142 A CCDS55780.1 CCDS55780.1 Transcript intron_variant - - - - - - rs667232 11:77805891 A - - - intergenic_variant - - - - - - rs518624 11:77832076 A CCDS41692.1 CCDS41692.1 Transcript intron_variant - - - - - - rs518624 11:77832076 A ENSESTG00000009520 ENSESTT00000023920 Transcript intron_variant - - - - - - rs518624 11:77832076 A CCDS8258.1 CCDS8258.1 Transcript intron_variant - - - - - - rs518624 11:77832076 A 79053 NM_001007027.2 Transcript intron_variant - - - - - - rs518624 11:77832076 A ENSESTG00000009520 ENSESTT00000023928 Transcript intron_variant - - - - - - rs518624 11:77832076 A ENSESTG00000009520 ENSESTT00000023936 Transcript intron_variant - - - - - - rs518624 11:77832076 A ENSESTG00000009520 ENSESTT00000023949 Transcript intron_variant - - - - - - rs518624 11:77832076 A 79053 NM_024079.4 Transcript intron_variant - - - - - - rs518624 11:77832076 A ENSESTG00000009520 ENSESTT00000023945 Transcript intron_variant - - - - - - rs518624 11:77832076 A ENSESTG00000009520 ENSESTT00000023873 Transcript downstream_gene_variant - - - - - - DISTANCE=2993 rs518624 11:77832076 A ENSESTG00000009520 ENSESTT00000023940 Transcript intron_variant - - - - - - rs7102431 11:78149435 G ENSESTG00000009450 ENSESTT00000023734 Transcript intron_variant - - - - - - rs7102431 11:78149435 G ENSESTG00000009450 ENSESTT00000023732 Transcript downstream_gene_variant - - - - - - DISTANCE=2704 rs7102431 11:78149435 G ENSESTG00000009450 ENSESTT00000023728 Transcript intron_variant - - - - - - rs7102431 11:78149435 G CCDS8261.1 CCDS8261.1 Transcript intron_variant - - - - - - rs7102431 11:78149435 G CCDS58164.1 CCDS58164.1 Transcript intron_variant - - - - - - rs7102431 11:78149435 G 79731 NM_001243251.1 Transcript intron_variant - - - - - - rs7102431 11:78149435 G 79731 NM_024678.5 Transcript intron_variant - - - - - - rs7118441 11:78216146 A ENSESTG00000009450 ENSESTT00000023734 Transcript intron_variant - - - - - - rs7118441 11:78216146 A ENSESTG00000009450 ENSESTT00000023732 Transcript intron_variant - - - - - - rs7118441 11:78216146 A ENSESTG00000009450 ENSESTT00000023728 Transcript intron_variant - - - - - - rs7118441 11:78216146 A CCDS8261.1 CCDS8261.1 Transcript intron_variant - - - - - - rs7118441 11:78216146 A CCDS58164.1 CCDS58164.1 Transcript intron_variant - - - - - - rs7118441 11:78216146 A 79731 NM_001243251.1 Transcript intron_variant - - - - - - rs7118441 11:78216146 A 79731 NM_024678.5 Transcript intron_variant - - - - - - rs4945283 11:78216457 A ENSESTG00000009450 ENSESTT00000023734 Transcript intron_variant - - - - - - rs4945283 11:78216457 A ENSESTG00000009450 ENSESTT00000023732 Transcript intron_variant - - - - - - rs4945283 11:78216457 A ENSESTG00000009450 ENSESTT00000023728 Transcript intron_variant - - - - - - rs4945283 11:78216457 A CCDS8261.1 CCDS8261.1 Transcript intron_variant - - - - - - rs4945283 11:78216457 A CCDS58164.1 CCDS58164.1 Transcript intron_variant - - - - - - rs4945283 11:78216457 A 79731 NM_001243251.1 Transcript intron_variant - - - - - - rs4945283 11:78216457 A 79731 NM_024678.5 Transcript intron_variant - - - - - - rs491728 11:78526084 G CCDS44688.1 CCDS44688.1 Transcript intron_variant - - - - - - rs491728 11:78526084 G 26011 NM_001098816.2 Transcript intron_variant - - - - - - rs491728 11:78526084 G ENSESTG00000001371 ENSESTT00000003243 Transcript upstream_gene_variant - - - - - - DISTANCE=609 rs588128 11:78729657 G - ENSR00000566027 RegulatoryFeature regulatory_region_variant - - - - - - rs588128 11:78729657 G CCDS44688.1 CCDS44688.1 Transcript intron_variant - - - - - - rs588128 11:78729657 G 26011 NM_001098816.2 Transcript intron_variant - - - - - - rs588128 11:78729657 G ENSESTG00000001315 ENSESTT00000003108 Transcript upstream_gene_variant - - - - - - DISTANCE=3961 rs561455 11:79099552 C - ENSR00001571835 RegulatoryFeature regulatory_region_variant - - - - - - rs561455 11:79099552 C 26011 NM_001098816.2 Transcript intron_variant - - - - - - rs561455 11:79099552 C ENSESTG00000001313 ENSESTT00000003100 Transcript intron_variant - - - - - - rs561455 11:79099552 C ENSESTG00000001295 ENSESTT00000003055 Transcript intron_variant - - - - - - rs561455 11:79099552 C ENSESTG00000001295 ENSESTT00000003062 Transcript intron_variant - - - - - - rs561455 11:79099552 C ENSESTG00000001295 ENSESTT00000003059 Transcript intron_variant - - - - - - rs1944716 11:79262089 C ENSESTG00000001285 ENSESTT00000003028 Transcript intron_variant - - - - - - rs1944706 11:79278520 G ENSESTG00000001285 ENSESTT00000003028 Transcript intron_variant - - - - - - rs1944709 11:79287713 G ENSESTG00000001285 ENSESTT00000003028 Transcript intron_variant - - - - - - rs2663190 11:79475907 A - - - intergenic_variant - - - - - - rs1944949 11:79491478 A - - - intergenic_variant - - - - - - rs656651 11:79543491 G - - - intergenic_variant - - - - - - rs650085 11:79799245 A - - - intergenic_variant - - - - - - rs2850801 11:79820581 G - - - intergenic_variant - - - - - - rs7479489 11:80017542 A - - - intergenic_variant - - - - - - rs7947638 11:80786475 A - - - intergenic_variant - - - - - - rs2512107 11:80847884 T - - - intergenic_variant - - - - - - rs2514468 11:81010741 T - - - intergenic_variant - - - - - - rs10792544 11:81025699 A - - - intergenic_variant - - - - - - rs2168820 11:81060849 C - - - intergenic_variant - - - - - - rs7932211 11:81078765 G - - - intergenic_variant - - - - - - rs7940133 11:81502826 A - - - intergenic_variant - - - - - - rs4483611 11:82040939 A - - - intergenic_variant - - - - - - rs1399345 11:82146281 T - - - intergenic_variant - - - - - - rs587863 11:83275693 T ENSESTG00000019302 ENSESTT00000048568 Transcript intron_variant - - - - - - rs587863 11:83275693 T CCDS44692.1 CCDS44692.1 Transcript intron_variant - - - - - - rs587863 11:83275693 T CCDS41696.1 CCDS41696.1 Transcript intron_variant - - - - - - rs587863 11:83275693 T 1740 NM_001142702.1 Transcript intron_variant - - - - - - rs587863 11:83275693 T CCDS55782.1 CCDS55782.1 Transcript intron_variant - - - - - - rs587863 11:83275693 T ENSESTG00000019302 ENSESTT00000048553 Transcript intron_variant - - - - - - rs587863 11:83275693 T 1740 NM_001142700.1 Transcript intron_variant - - - - - - rs587863 11:83275693 T 1740 NM_001142699.1 Transcript intron_variant - - - - - - rs587863 11:83275693 T CCDS44691.1 CCDS44691.1 Transcript intron_variant - - - - - - rs587863 11:83275693 T ENSESTG00000019302 ENSESTT00000048497 Transcript intron_variant - - - - - - rs587863 11:83275693 T 1740 NM_001206769.1 Transcript intron_variant - - - - - - rs587863 11:83275693 T ENSESTG00000019302 ENSESTT00000048488 Transcript intron_variant - - - - - - rs587863 11:83275693 T 1740 NM_001364.3 Transcript intron_variant - - - - - - rs587863 11:83275693 T CCDS44690.1 CCDS44690.1 Transcript intron_variant - - - - - - rs2508718 11:83291371 A ENSESTG00000019302 ENSESTT00000048568 Transcript intron_variant - - - - - - rs2508718 11:83291371 A CCDS44692.1 CCDS44692.1 Transcript intron_variant - - - - - - rs2508718 11:83291371 A CCDS41696.1 CCDS41696.1 Transcript intron_variant - - - - - - rs2508718 11:83291371 A 1740 NM_001142702.1 Transcript intron_variant - - - - - - rs2508718 11:83291371 A CCDS55782.1 CCDS55782.1 Transcript intron_variant - - - - - - rs2508718 11:83291371 A ENSESTG00000019302 ENSESTT00000048553 Transcript intron_variant - - - - - - rs2508718 11:83291371 A 1740 NM_001142700.1 Transcript intron_variant - - - - - - rs2508718 11:83291371 A 1740 NM_001142699.1 Transcript intron_variant - - - - - - rs2508718 11:83291371 A CCDS44691.1 CCDS44691.1 Transcript intron_variant - - - - - - rs2508718 11:83291371 A ENSESTG00000019302 ENSESTT00000048497 Transcript intron_variant - - - - - - rs2508718 11:83291371 A 1740 NM_001206769.1 Transcript intron_variant - - - - - - rs2508718 11:83291371 A ENSESTG00000019302 ENSESTT00000048488 Transcript intron_variant - - - - - - rs2508718 11:83291371 A 1740 NM_001364.3 Transcript intron_variant - - - - - - rs2508718 11:83291371 A CCDS44690.1 CCDS44690.1 Transcript intron_variant - - - - - - rs2508721 11:83308789 C ENSESTG00000019302 ENSESTT00000048568 Transcript intron_variant - - - - - - rs2508721 11:83308789 C CCDS44692.1 CCDS44692.1 Transcript intron_variant - - - - - - rs2508721 11:83308789 C CCDS41696.1 CCDS41696.1 Transcript intron_variant - - - - - - rs2508721 11:83308789 C 1740 NM_001142702.1 Transcript intron_variant - - - - - - rs2508721 11:83308789 C CCDS55782.1 CCDS55782.1 Transcript intron_variant - - - - - - rs2508721 11:83308789 C ENSESTG00000019302 ENSESTT00000048553 Transcript intron_variant - - - - - - rs2508721 11:83308789 C 1740 NM_001142700.1 Transcript intron_variant - - - - - - rs2508721 11:83308789 C 1740 NM_001142699.1 Transcript intron_variant - - - - - - rs2508721 11:83308789 C CCDS44691.1 CCDS44691.1 Transcript intron_variant - - - - - - rs2508721 11:83308789 C ENSESTG00000019302 ENSESTT00000048497 Transcript intron_variant - - - - - - rs2508721 11:83308789 C 1740 NM_001206769.1 Transcript intron_variant - - - - - - rs2508721 11:83308789 C ENSESTG00000019302 ENSESTT00000048488 Transcript intron_variant - - - - - - rs2508721 11:83308789 C 1740 NM_001364.3 Transcript intron_variant - - - - - - rs2508721 11:83308789 C CCDS44690.1 CCDS44690.1 Transcript intron_variant - - - - - - rs497917 11:83321322 G ENSESTG00000019302 ENSESTT00000048568 Transcript intron_variant - - - - - - rs497917 11:83321322 G CCDS44692.1 CCDS44692.1 Transcript intron_variant - - - - - - rs497917 11:83321322 G CCDS41696.1 CCDS41696.1 Transcript intron_variant - - - - - - rs497917 11:83321322 G 1740 NM_001142702.1 Transcript intron_variant - - - - - - rs497917 11:83321322 G CCDS55782.1 CCDS55782.1 Transcript intron_variant - - - - - - rs497917 11:83321322 G ENSESTG00000019302 ENSESTT00000048553 Transcript intron_variant - - - - - - rs497917 11:83321322 G 1740 NM_001142700.1 Transcript intron_variant - - - - - - rs497917 11:83321322 G 1740 NM_001142699.1 Transcript intron_variant - - - - - - rs497917 11:83321322 G CCDS44691.1 CCDS44691.1 Transcript intron_variant - - - - - - rs497917 11:83321322 G ENSESTG00000019302 ENSESTT00000048497 Transcript intron_variant - - - - - - rs497917 11:83321322 G 1740 NM_001206769.1 Transcript intron_variant - - - - - - rs497917 11:83321322 G ENSESTG00000019302 ENSESTT00000048488 Transcript intron_variant - - - - - - rs497917 11:83321322 G 1740 NM_001364.3 Transcript intron_variant - - - - - - rs497917 11:83321322 G CCDS44690.1 CCDS44690.1 Transcript intron_variant - - - - - - rs570632 11:84231850 T 1740 NM_001142699.1 Transcript intron_variant - - - - - - rs570632 11:84231850 T CCDS41696.1 CCDS41696.1 Transcript intron_variant - - - - - - rs570632 11:84231850 T CCDS44690.1 CCDS44690.1 Transcript intron_variant - - - - - - rs570632 11:84231850 T 1740 NM_001364.3 Transcript intron_variant - - - - - - rs10751117 11:84650819 A 1740 NM_001142699.1 Transcript intron_variant - - - - - - rs10751117 11:84650819 A CCDS44690.1 CCDS44690.1 Transcript intron_variant - - - - - - rs595467 11:84740618 T 1740 NM_001142699.1 Transcript intron_variant - - - - - - rs595467 11:84740618 T CCDS44690.1 CCDS44690.1 Transcript intron_variant - - - - - - rs617246 11:85306337 T - ENSR00000110990 RegulatoryFeature regulatory_region_variant - - - - - - rs617246 11:85306337 T 1740 NM_001142699.1 Transcript intron_variant - - - - - - rs617246 11:85306337 T ENSESTG00000000729 ENSESTT00000001747 Transcript intron_variant - - - - - - rs617246 11:85306337 T ENSESTG00000000729 ENSESTT00000001736 Transcript intron_variant - - - - - - rs617246 11:85306337 T CCDS44690.1 CCDS44690.1 Transcript intron_variant - - - - - - rs631392 11:85340707 G ENSESTG00000000618 ENSESTT00000001498 Transcript intron_variant - - - - - - rs631392 11:85340707 G ENSESTG00000000729 ENSESTT00000001736 Transcript upstream_gene_variant - - - - - - DISTANCE=1914 rs631392 11:85340707 G ENSESTG00000000729 ENSESTT00000001741 Transcript upstream_gene_variant - - - - - - DISTANCE=1914 rs631392 11:85340707 G 55863 NM_018480.4 Transcript intron_variant - - - - - - rs631392 11:85340707 G CCDS8267.2 CCDS8267.2 Transcript intron_variant - - - - - - rs631392 11:85340707 G 1740 NM_001142699.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2393 rs631392 11:85340707 G ENSESTG00000000729 ENSESTT00000001747 Transcript upstream_gene_variant - - - - - - DISTANCE=1989 rs631392 11:85340707 G 55863 NM_001193538.2 Transcript intron_variant - - - - - - rs631392 11:85340707 G 55863 NM_001256546.1 Transcript intron_variant - - - - - - rs631392 11:85340707 G ENSESTG00000000618 ENSESTT00000001496 Transcript intron_variant - - - - - - rs631392 11:85340707 G 55863 NM_001193537.2 Transcript intron_variant - - - - - - rs631392 11:85340707 G CCDS53686.1 CCDS53686.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2033 rs631392 11:85340707 G 55863 NM_001256547.1 Transcript intron_variant - - - - - - rs686426 11:85357211 T CCDS8268.1 CCDS8268.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4089 rs686426 11:85357211 T 84233 NM_032273.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1752 rs686426 11:85357211 T 84233 NM_001244735.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1752 rs686426 11:85357211 T ENSESTG00000000648 ENSESTT00000001565 Transcript upstream_gene_variant - - - - - - DISTANCE=1752 rs515668 11:85442284 T CCDS31649.1 CCDS31649.1 Transcript intron_variant - - - - - - rs515668 11:85442284 T CCDS53689.1 CCDS53689.1 Transcript intron_variant - - - - - - rs515668 11:85442284 T CCDS53688.1 CCDS53688.1 Transcript intron_variant - - - - - - rs515668 11:85442284 T 54843 NM_032943.3 Transcript intron_variant - - - - - - rs515668 11:85442284 T 54843 NM_206927.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4773 rs515668 11:85442284 T 54843 NM_001162953.1 Transcript intron_variant - - - - - - rs515668 11:85442284 T 54843 NM_206928.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4773 rs515668 11:85442284 T ENSESTG00000014210 ENSESTT00000035590 Transcript intron_variant - - - - - - rs515668 11:85442284 T CCDS31650.1 CCDS31650.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4785 rs515668 11:85442284 T 54843 NM_001162951.1 Transcript intron_variant - - - - - - rs515668 11:85442284 T CCDS31651.1 CCDS31651.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4785 rs6592262 11:85601887 G ENSESTG00000013948 ENSESTT00000034874 Transcript intron_variant - - - - - - rs6592262 11:85601887 G 220047 NM_173556.3 Transcript intron_variant - - - - - - rs6592262 11:85601887 G CCDS8271.1 CCDS8271.1 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035500 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035387 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035467 Transcript intron_variant - - - - - - rs2508689 11:85704184 A 8301 NM_001206946.1 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035415 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035436 Transcript intron_variant - - - - - - rs2508689 11:85704184 A CCDS8272.1 CCDS8272.1 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035429 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035384 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035507 Transcript intron_variant - - - - - - rs2508689 11:85704184 A 8301 NM_001008660.2 Transcript intron_variant - - - - - - rs2508689 11:85704184 A 8301 NM_007166.3 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035408 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035402 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035497 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035411 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035378 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035400 Transcript intron_variant - - - - - - rs2508689 11:85704184 A 8301 NM_001206947.1 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035493 Transcript intron_variant - - - - - - rs2508689 11:85704184 A CCDS55784.1 CCDS55784.1 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035491 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035504 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035483 Transcript intron_variant - - - - - - rs2508689 11:85704184 A CCDS31653.1 CCDS31653.1 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035413 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035421 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035389 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035470 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035397 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035487 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035426 Transcript intron_variant - - - - - - rs2508689 11:85704184 A CCDS55783.1 CCDS55783.1 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035404 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035431 Transcript intron_variant - - - - - - rs2508689 11:85704184 A ENSESTG00000014126 ENSESTT00000035472 Transcript intron_variant - - - - - - rs606584 11:85790408 A - - - intergenic_variant - - - - - - rs1472421 11:85944584 A - - - intergenic_variant - - - - - - rs2454098 11:86030341 A ENSESTG00000013991 ENSESTT00000035001 Transcript intron_variant - - - - - - rs2454098 11:86030341 A 51501 NM_016401.3 Transcript intron_variant - - - - - - rs2454098 11:86030341 A ENSESTG00000013991 ENSESTT00000035009 Transcript intron_variant - - - - - - rs2454098 11:86030341 A 51501 NR_024597.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2454098 11:86030341 A 51501 NR_024598.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2454098 11:86030341 A ENSESTG00000013991 ENSESTT00000035017 Transcript intron_variant - - - - - - rs2454098 11:86030341 A CCDS8275.1 CCDS8275.1 Transcript intron_variant - - - - - - rs2454098 11:86030341 A 51501 NR_024596.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs291219 11:86034929 A ENSESTG00000013991 ENSESTT00000035001 Transcript intron_variant - - - - - - rs291219 11:86034929 A 51501 NM_016401.3 Transcript intron_variant - - - - - - rs291219 11:86034929 A ENSESTG00000013991 ENSESTT00000035009 Transcript intron_variant - - - - - - rs291219 11:86034929 A 51501 NR_024597.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs291219 11:86034929 A 51501 NR_024598.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs291219 11:86034929 A ENSESTG00000013991 ENSESTT00000035017 Transcript intron_variant - - - - - - rs291219 11:86034929 A CCDS8275.1 CCDS8275.1 Transcript intron_variant - - - - - - rs291219 11:86034929 A 51501 NR_024596.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs176762 11:86110146 T ENSESTG00000014028 ENSESTT00000035087 Transcript intron_variant - - - - - - rs176762 11:86110146 T ENSESTG00000014028 ENSESTT00000035077 Transcript intron_variant - - - - - - rs176762 11:86110146 T CCDS53691.1 CCDS53691.1 Transcript intron_variant - - - - - - rs176762 11:86110146 T ENSESTG00000014028 ENSESTT00000035095 Transcript intron_variant - - - - - - rs176762 11:86110146 T CCDS8276.1 CCDS8276.1 Transcript intron_variant - - - - - - rs176762 11:86110146 T 60494 NM_001156474.1 Transcript intron_variant - - - - - - rs176762 11:86110146 T 60494 NM_021827.4 Transcript intron_variant - - - - - - rs635971 11:86283673 A ENSESTG00000014046 ENSESTT00000035109 Transcript intron_variant - - - - - - rs635971 11:86283673 A 10873 NM_001161586.1 Transcript intron_variant - - - - - - rs635971 11:86283673 A CCDS8277.1 CCDS8277.1 Transcript intron_variant - - - - - - rs635971 11:86283673 A ENSESTG00000014053 ENSESTT00000035156 Transcript intron_variant - - - - - - rs635971 11:86283673 A ENSESTG00000014053 ENSESTT00000035176 Transcript intron_variant - - - - - - rs635971 11:86283673 A 10873 NM_001014811.1 Transcript intron_variant - - - - - - rs635971 11:86283673 A 10873 NM_006680.2 Transcript intron_variant - - - - - - rs635971 11:86283673 A ENSESTG00000014053 ENSESTT00000035163 Transcript intron_variant - - - - - - rs635971 11:86283673 A ENSESTG00000014053 ENSESTT00000035179 Transcript intron_variant - - - - - - rs593450 11:86332381 C - ENSR00001572119 RegulatoryFeature regulatory_region_variant - - - - - - rs593450 11:86332381 C ENSESTG00000014046 ENSESTT00000035109 Transcript intron_variant - - - - - - rs593450 11:86332381 C 10873 NM_001161586.1 Transcript intron_variant - - - - - - rs593450 11:86332381 C CCDS8277.1 CCDS8277.1 Transcript intron_variant - - - - - - rs593450 11:86332381 C ENSESTG00000014053 ENSESTT00000035156 Transcript intron_variant - - - - - - rs593450 11:86332381 C ENSESTG00000014053 ENSESTT00000035176 Transcript intron_variant - - - - - - rs593450 11:86332381 C 10873 NM_001014811.1 Transcript intron_variant - - - - - - rs593450 11:86332381 C 10873 NM_006680.2 Transcript intron_variant - - - - - - rs593450 11:86332381 C ENSESTG00000014053 ENSESTT00000035163 Transcript intron_variant - - - - - - rs593450 11:86332381 C ENSESTG00000014053 ENSESTT00000035179 Transcript intron_variant - - - - - - rs9971411 11:86638671 G ENSESTG00000029683 ENSESTT00000074699 Transcript intron_variant - - - - - - rs9971411 11:86638671 G ENSESTG00000029683 ENSESTT00000074658 Transcript intron_variant - - - - - - rs9971411 11:86638671 G ENSESTG00000029972 ENSESTT00000075376 Transcript upstream_gene_variant - - - - - - DISTANCE=2592 rs9971411 11:86638671 G ENSESTG00000029683 ENSESTT00000074710 Transcript intron_variant - - - - - - rs10792900 11:86736282 G ENSESTG00000029934 ENSESTT00000075315 Transcript intron_variant - - - - - - rs10792900 11:86736282 G ENSESTG00000029934 ENSESTT00000075270 Transcript downstream_gene_variant - - - - - - DISTANCE=327 rs7112344 11:87032215 C CCDS8280.1 CCDS8280.1 Transcript intron_variant - - - - - - rs7112344 11:87032215 C CCDS53692.1 CCDS53692.1 Transcript intron_variant - - - - - - rs7112344 11:87032215 C ENSESTG00000029919 ENSESTT00000075227 Transcript downstream_gene_variant - - - - - - DISTANCE=782 rs7112344 11:87032215 C ENSESTG00000029784 ENSESTT00000075159 Transcript intron_variant - - - - - - rs7112344 11:87032215 C ENSESTG00000029784 ENSESTT00000075190 Transcript intron_variant - - - - - - rs7112344 11:87032215 C 65084 NR_033149.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7112344 11:87032215 C 65084 NM_001168724.1 Transcript intron_variant - - - - - - rs7112344 11:87032215 C ENSESTG00000029784 ENSESTT00000075151 Transcript intron_variant - - - - - - rs7112344 11:87032215 C 65084 NM_022918.3 Transcript intron_variant - - - - - - rs7112344 11:87032215 C ENSESTG00000029784 ENSESTT00000075174 Transcript intron_variant - - - - - - rs7112344 11:87032215 C ENSESTG00000029784 ENSESTT00000075195 Transcript intron_variant - - - - - - rs4418841 11:87066351 T - - - intergenic_variant - - - - - - rs4542443 11:87233909 A - - - intergenic_variant - - - - - - rs6592379 11:87239187 G - - - intergenic_variant - - - - - - rs4259845 11:87242689 T - - - intergenic_variant - - - - - - rs2155189 11:87443051 T - - - intergenic_variant - - - - - - rs10751179 11:87462395 A - - - intergenic_variant - - - - - - rs6592439 11:87531702 G - - - intergenic_variant - - - - - - rs663058 11:87634551 C - - - intergenic_variant - - - - - - rs308868 11:88185542 T - - - intergenic_variant - - - - - - rs188674 11:88190712 A - - - intergenic_variant - - - - - - rs7926399 11:88760714 C CCDS44694.1 CCDS44694.1 Transcript intron_variant - - - - - - rs7926399 11:88760714 C 2915 NM_000842.3 Transcript intron_variant - - - - - - rs7926399 11:88760714 C 2915 NM_001143831.2 Transcript intron_variant - - - - - - rs7926399 11:88760714 C CCDS8283.1 CCDS8283.1 Transcript intron_variant - - - - - - rs535527 11:88928561 T CCDS8284.1 CCDS8284.1 Transcript intron_variant - - - - - - rs535527 11:88928561 T ENSESTG00000015583 ENSESTT00000039068 Transcript intron_variant - - - - - - rs535527 11:88928561 T 7299 NM_000372.4 Transcript intron_variant - - - - - - rs1783963 11:88991191 C CCDS8284.1 CCDS8284.1 Transcript intron_variant - - - - - - rs1783963 11:88991191 C ENSESTG00000015583 ENSESTT00000039068 Transcript intron_variant - - - - - - rs1783963 11:88991191 C 7299 NM_000372.4 Transcript intron_variant - - - - - - rs317158 11:89128962 G ENSESTG00000015609 ENSESTT00000039112 Transcript intron_variant - - - - - - rs317158 11:89128962 G 50507 NM_016931.3 Transcript intron_variant - - - - - - rs317158 11:89128962 G CCDS44695.1 CCDS44695.1 Transcript intron_variant - - - - - - rs317158 11:89128962 G ENSESTG00000015609 ENSESTT00000039141 Transcript intron_variant - - - - - - rs317158 11:89128962 G 50507 NM_001143836.1 Transcript intron_variant - - - - - - rs317158 11:89128962 G ENSESTG00000015609 ENSESTT00000039139 Transcript intron_variant - - - - - - rs317158 11:89128962 G CCDS44696.1 CCDS44696.1 Transcript intron_variant - - - - - - rs317158 11:89128962 G 50507 NR_026571.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs317158 11:89128962 G 50507 NM_001143837.1 Transcript intron_variant - - - - - - rs317158 11:89128962 G ENSESTG00000015609 ENSESTT00000039168 Transcript intron_variant - - - - - - rs317158 11:89128962 G CCDS8285.1 CCDS8285.1 Transcript intron_variant - - - - - - rs319028 11:89178093 C ENSESTG00000015609 ENSESTT00000039112 Transcript intron_variant - - - - - - rs319028 11:89178093 C 50507 NM_016931.3 Transcript intron_variant - - - - - - rs319028 11:89178093 C CCDS44695.1 CCDS44695.1 Transcript intron_variant - - - - - - rs319028 11:89178093 C ENSESTG00000015609 ENSESTT00000039141 Transcript intron_variant - - - - - - rs319028 11:89178093 C 50507 NM_001143836.1 Transcript intron_variant - - - - - - rs319028 11:89178093 C ENSESTG00000015609 ENSESTT00000039139 Transcript intron_variant - - - - - - rs319028 11:89178093 C ENSESTG00000015609 ENSESTT00000039124 Transcript intron_variant - - - - - - rs319028 11:89178093 C CCDS44696.1 CCDS44696.1 Transcript intron_variant - - - - - - rs319028 11:89178093 C 50507 NR_026571.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs319028 11:89178093 C 50507 NM_001143837.1 Transcript intron_variant - - - - - - rs319028 11:89178093 C ENSESTG00000015609 ENSESTT00000039168 Transcript intron_variant - - - - - - rs319028 11:89178093 C CCDS8285.1 CCDS8285.1 Transcript intron_variant - - - - - - rs2508387 11:89853568 G - - - intergenic_variant - - - - - - rs492848 11:89938997 G ENSESTG00000013916 ENSESTT00000034768 Transcript downstream_gene_variant - - - - - - DISTANCE=4729 rs492848 11:89938997 G 26973 NM_001144073.1 Transcript intron_variant - - - - - - rs492848 11:89938997 G CCDS8289.1 CCDS8289.1 Transcript intron_variant - - - - - - rs492848 11:89938997 G ENSESTG00000013916 ENSESTT00000034787 Transcript downstream_gene_variant - - - - - - DISTANCE=403 rs492848 11:89938997 G CCDS44705.1 CCDS44705.1 Transcript intron_variant - - - - - - rs492848 11:89938997 G ENSESTG00000013916 ENSESTT00000034774 Transcript downstream_gene_variant - - - - - - DISTANCE=4742 rs492848 11:89938997 G 26973 NM_012124.2 Transcript intron_variant - - - - - - rs7943212 11:90002274 A - - - intergenic_variant - - - - - - rs663004 11:90366258 A - - - intergenic_variant - - - - - - rs2514092 11:90785626 G - - - intergenic_variant - - - - - - rs2463845 11:90901925 A ENSESTG00000031139 ENSESTT00000078399 Transcript downstream_gene_variant - - - - - - DISTANCE=1495 rs7946915 11:90905593 A - - - intergenic_variant - - - - - - rs2514920 11:90940498 T - - - intergenic_variant - - - - - - rs2514922 11:90951734 C - - - intergenic_variant - - - - - - rs7949535 11:91233629 T - - - intergenic_variant - - - - - - rs1491681 11:91550270 T ENSESTG00000005490 ENSESTT00000013983 Transcript downstream_gene_variant - - - - - - DISTANCE=4810 rs2512969 11:91896725 A - - - intergenic_variant - - - - - - rs6483177 11:92061867 C - - - intergenic_variant - - - - - - rs572760 11:92179901 A ENSESTG00000005502 ENSESTT00000014020 Transcript intron_variant - - - - - - rs572760 11:92179901 A ENSESTG00000005496 ENSESTT00000014009 Transcript intron_variant - - - - - - rs572760 11:92179901 A 120114 NM_001008781.2 Transcript intron_variant - - - - - - rs568607 11:92267914 T 120114 NM_001008781.2 Transcript intron_variant - - - - - - rs577246 11:92363496 G 120114 NM_001008781.2 Transcript intron_variant - - - - - - rs3018346 11:93997837 A - - - intergenic_variant - - - - - - rs3017078 11:94160819 A CCDS8299.1 CCDS8299.1 Transcript intron_variant - - - - - - rs3017078 11:94160819 A ENSESTG00000005591 ENSESTT00000014252 Transcript intron_variant - - - - - - rs3017078 11:94160819 A CCDS8298.1 CCDS8298.1 Transcript intron_variant - - - - - - rs3017078 11:94160819 A 4361 NM_005590.3 Transcript intron_variant - - - - - - rs3017078 11:94160819 A 4361 NM_005591.3 Transcript intron_variant - - - - - - rs4258334 11:94257823 A ENSESTG00000005461 ENSESTT00000013886 Transcript upstream_gene_variant - - - - - - DISTANCE=3424 rs4258334 11:94257823 A 643037 NM_001190462.1 Transcript intron_variant - - - - - - rs4258334 11:94257823 A ENSESTG00000005461 ENSESTT00000013884 Transcript intron_variant - - - - - - rs4453197 11:94264753 A ENSESTG00000005461 ENSESTT00000013886 Transcript intron_variant - - - - - - rs4453197 11:94264753 A 643037 NM_001190462.1 Transcript intron_variant - - - - - - rs4453197 11:94264753 A ENSESTG00000005461 ENSESTT00000013884 Transcript intron_variant - - - - - - rs2508461 11:94303180 T CCDS31656.1 CCDS31656.1 Transcript intron_variant - - - - - - rs2508461 11:94303180 T 143689 NM_152431.2 Transcript intron_variant - - - - - - rs2508461 11:94303180 T ENSESTG00000005579 ENSESTT00000014178 Transcript intron_variant - - - - - - rs2508461 11:94303180 T ENSESTG00000005579 ENSESTT00000014180 Transcript intron_variant - - - - - - rs2508461 11:94303180 T ENSESTG00000005467 ENSESTT00000013907 Transcript intron_variant - - - - - - rs2508461 11:94303180 T ENSESTG00000005467 ENSESTT00000013900 Transcript intron_variant - - - - - - rs2915240 11:94473281 T ENSESTG00000005579 ENSESTT00000014178 Transcript intron_variant - - - - - - rs2915240 11:94473281 T ENSESTG00000005579 ENSESTT00000014180 Transcript intron_variant - - - - - - rs2915240 11:94473281 T ENSESTG00000016337 ENSESTT00000040992 Transcript intron_variant - - - - - - rs2450284 11:94575825 T CCDS44712.1 CCDS44712.1 Transcript intron_variant - - - - - - rs2450284 11:94575825 T 154810 NM_130847.2 Transcript intron_variant - - - - - - rs2450284 11:94575825 T ENSESTG00000016352 ENSESTT00000041094 Transcript intron_variant - - - - - - rs2450284 11:94575825 T ENSESTG00000016352 ENSESTT00000041103 Transcript intron_variant - - - - - - rs2450284 11:94575825 T ENSESTG00000016548 ENSESTT00000041487 Transcript intron_variant - - - - - - rs2450283 11:94575834 T CCDS44712.1 CCDS44712.1 Transcript intron_variant - - - - - - rs2450283 11:94575834 T 154810 NM_130847.2 Transcript intron_variant - - - - - - rs2450283 11:94575834 T ENSESTG00000016352 ENSESTT00000041094 Transcript intron_variant - - - - - - rs2450283 11:94575834 T ENSESTG00000016352 ENSESTT00000041103 Transcript intron_variant - - - - - - rs2450283 11:94575834 T ENSESTG00000016548 ENSESTT00000041487 Transcript intron_variant - - - - - - rs4753640 11:94632798 T - - - intergenic_variant - - - - - - rs2509624 11:94632817 T - - - intergenic_variant - - - - - - rs10765708 11:94749192 G - - - intergenic_variant - - - - - - rs7119113 11:94749334 A - - - intergenic_variant - - - - - - rs3016947 11:94823448 T - ENSR00001572594 RegulatoryFeature regulatory_region_variant - - - - - - rs3016947 11:94823448 T CCDS41699.1 CCDS41699.1 Transcript intron_variant - - - - - - rs3016947 11:94823448 T ENSESTG00000016397 ENSESTT00000041149 Transcript intron_variant - - - - - - rs3016947 11:94823448 T 23052 NM_015036.2 Transcript intron_variant - - - - - - rs1255834 11:95004860 A - - - intergenic_variant - - - - - - rs3108464 11:95466827 T - - - intergenic_variant - - - - - - rs3133081 11:95468300 G - - - intergenic_variant - - - - - - rs3108465 11:95468317 T - - - intergenic_variant - - - - - - rs3016523 11:95632582 A ENSESTG00000021984 ENSESTT00000055386 Transcript intron_variant - - - - - - rs3016523 11:95632582 A 8898 NM_016156.5 Transcript intron_variant - - - - - - rs3016523 11:95632582 A 8898 NM_201281.2 Transcript intron_variant - - - - - - rs3016523 11:95632582 A CCDS8305.1 CCDS8305.1 Transcript intron_variant - - - - - - rs3016523 11:95632582 A ENSESTG00000021984 ENSESTT00000055505 Transcript intron_variant - - - - - - rs3016523 11:95632582 A ENSESTG00000021984 ENSESTT00000055393 Transcript intron_variant - - - - - - rs3016523 11:95632582 A ENSESTG00000021984 ENSESTT00000055416 Transcript intron_variant - - - - - - rs3016523 11:95632582 A ENSESTG00000021984 ENSESTT00000055403 Transcript intron_variant - - - - - - rs3016523 11:95632582 A 8898 NM_201278.2 Transcript intron_variant - - - - - - rs3016523 11:95632582 A 8898 NM_001243571.1 Transcript intron_variant - - - - - - rs3016523 11:95632582 A ENSESTG00000021984 ENSESTT00000055536 Transcript intron_variant - - - - - - rs3016512 11:95700517 T - - - intergenic_variant - - - - - - rs4497365 11:95750234 T ENSESTG00000021974 ENSESTT00000055278 Transcript intron_variant - - - - - - rs4497365 11:95750234 T ENSESTG00000021974 ENSESTT00000055287 Transcript intron_variant - - - - - - rs4497365 11:95750234 T ENSESTG00000021974 ENSESTT00000055296 Transcript intron_variant - - - - - - rs4497365 11:95750234 T CCDS44714.1 CCDS44714.1 Transcript intron_variant - - - - - - rs4497365 11:95750234 T 84441 NM_032427.1 Transcript intron_variant - - - - - - rs4497365 11:95750234 T ENSESTG00000021974 ENSESTT00000055277 Transcript intron_variant - - - - - - rs2508763 11:95881549 A CCDS44714.1 CCDS44714.1 Transcript intron_variant - - - - - - rs2508763 11:95881549 A 84441 NM_032427.1 Transcript intron_variant - - - - - - rs2508444 11:96066555 T - ENSR00000567560 RegulatoryFeature regulatory_region_variant - - - - - - rs2508444 11:96066555 T CCDS44714.1 CCDS44714.1 Transcript intron_variant - - - - - - rs2508444 11:96066555 T 84441 NM_032427.1 Transcript intron_variant - - - - - - rs28766941 11:96444486 T - - - intergenic_variant - - - - - - rs991288 11:96636340 T - - - intergenic_variant - - - - - - rs575516 11:96819349 T - - - intergenic_variant - - - - - - rs1939292 11:96871211 C - - - intergenic_variant - - - - - - rs826001 11:97276973 T - - - intergenic_variant - - - - - - rs10736432 11:97472616 C - - - intergenic_variant - - - - - - rs4319479 11:97823741 T - - - intergenic_variant - - - - - - rs7126885 11:97843714 T - ENSR00000321197 RegulatoryFeature regulatory_region_variant - - - - - - rs7126885 11:97843714 T - - - intergenic_variant - - - - - - rs10891157 11:97863245 A - - - intergenic_variant - - - - - - rs694179 11:97929396 T - - - intergenic_variant - - - - - - rs2187032 11:98231339 C - - - intergenic_variant - - - - - - rs1115268 11:98310450 A - - - intergenic_variant - - - - - - rs4754519 11:98384782 A - - - intergenic_variant - - - - - - rs1601688 11:98751580 G - - - intergenic_variant - - - - - - rs4397812 11:98917586 A 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs4397812 11:98917586 A ENSESTG00000008223 ENSESTT00000020764 Transcript intron_variant - - - - - - rs4397812 11:98917586 A 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs4397812 11:98917586 A 53942 NM_014361.3 Transcript intron_variant - - - - - - rs6421577 11:98941438 A 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs6421577 11:98941438 A 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs6421577 11:98941438 A 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7117309 11:99123262 A 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7117309 11:99123262 A 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7117309 11:99123262 A 53942 NM_014361.3 Transcript intron_variant - - - - - - rs1224266 11:99143066 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs1224266 11:99143066 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs1224266 11:99143066 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7924989 11:99238921 C 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7924989 11:99238921 C 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7924989 11:99238921 C 53942 NM_014361.3 Transcript intron_variant - - - - - - rs4753951 11:99269831 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs4753951 11:99269831 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs4753951 11:99269831 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7106164 11:99283532 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7106164 11:99283532 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7106164 11:99283532 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs2245666 11:99288704 C 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs2245666 11:99288704 C 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs2245666 11:99288704 C 53942 NM_014361.3 Transcript intron_variant - - - - - - rs1504740 11:99288997 G 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs1504740 11:99288997 G 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs1504740 11:99288997 G 53942 NM_014361.3 Transcript intron_variant - - - - - - rs2515388 11:99350818 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs2515388 11:99350818 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs2515388 11:99350818 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs982888 11:99362430 A 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs982888 11:99362430 A 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs982888 11:99362430 A 53942 NM_014361.3 Transcript intron_variant - - - - - - rs2656196 11:99367709 C 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs2656196 11:99367709 C 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs2656196 11:99367709 C 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7394704 11:99627770 C 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7394704 11:99627770 C CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7394704 11:99627770 C 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7394704 11:99627770 C 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7394704 11:99627770 C 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7394704 11:99627770 C CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7394704 11:99627770 C CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs2439604 11:99657722 A 53942 NM_175566.2 Transcript intron_variant - - - - - - rs2439604 11:99657722 A CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs2439604 11:99657722 A 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs2439604 11:99657722 A 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs2439604 11:99657722 A 53942 NM_014361.3 Transcript intron_variant - - - - - - rs2439604 11:99657722 A CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs2439604 11:99657722 A CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs1218989 11:99672891 G 53942 NM_175566.2 Transcript intron_variant - - - - - - rs1218989 11:99672891 G CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs1218989 11:99672891 G 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs1218989 11:99672891 G 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs1218989 11:99672891 G 53942 NM_014361.3 Transcript intron_variant - - - - - - rs1218989 11:99672891 G CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs1218989 11:99672891 G CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7127442 11:99722001 G 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7127442 11:99722001 G CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7127442 11:99722001 G CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7127442 11:99722001 G 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7127442 11:99722001 G CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7127442 11:99722001 G 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7127442 11:99722001 G 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7127442 11:99722001 G ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7110957 11:99722039 A 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7110957 11:99722039 A CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7110957 11:99722039 A CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7110957 11:99722039 A 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7110957 11:99722039 A CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7110957 11:99722039 A 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7110957 11:99722039 A 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7110957 11:99722039 A ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs10736572 11:99727384 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs10736572 11:99727384 T CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs10736572 11:99727384 T CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs10736572 11:99727384 T 53942 NM_175566.2 Transcript intron_variant - - - - - - rs10736572 11:99727384 T CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs10736572 11:99727384 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs10736572 11:99727384 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs10736572 11:99727384 T ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs10736573 11:99727394 A 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs10736573 11:99727394 A CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs10736573 11:99727394 A CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs10736573 11:99727394 A 53942 NM_175566.2 Transcript intron_variant - - - - - - rs10736573 11:99727394 A CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs10736573 11:99727394 A 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs10736573 11:99727394 A 53942 NM_014361.3 Transcript intron_variant - - - - - - rs10736573 11:99727394 A ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7121449 11:99729174 C 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7121449 11:99729174 C CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7121449 11:99729174 C CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7121449 11:99729174 C 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7121449 11:99729174 C CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7121449 11:99729174 C 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7121449 11:99729174 C 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7121449 11:99729174 C ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7122373 11:99729235 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7122373 11:99729235 T CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7122373 11:99729235 T CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7122373 11:99729235 T 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7122373 11:99729235 T CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7122373 11:99729235 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7122373 11:99729235 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7122373 11:99729235 T ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7943425 11:99729531 A 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7943425 11:99729531 A CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7943425 11:99729531 A CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7943425 11:99729531 A 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7943425 11:99729531 A CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7943425 11:99729531 A 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7943425 11:99729531 A 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7943425 11:99729531 A ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7930740 11:99729596 C 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7930740 11:99729596 C CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7930740 11:99729596 C CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7930740 11:99729596 C 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7930740 11:99729596 C CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7930740 11:99729596 C 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7930740 11:99729596 C 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7930740 11:99729596 C ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7943536 11:99729608 A 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7943536 11:99729608 A CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7943536 11:99729608 A CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7943536 11:99729608 A 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7943536 11:99729608 A CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7943536 11:99729608 A 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7943536 11:99729608 A 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7943536 11:99729608 A ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs12276237 11:99744126 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs12276237 11:99744126 T CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs12276237 11:99744126 T CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs12276237 11:99744126 T 53942 NM_175566.2 Transcript intron_variant - - - - - - rs12276237 11:99744126 T CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs12276237 11:99744126 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs12276237 11:99744126 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs12276237 11:99744126 T ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7131639 11:99760120 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7131639 11:99760120 T CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7131639 11:99760120 T CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7131639 11:99760120 T 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7131639 11:99760120 T CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7131639 11:99760120 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7131639 11:99760120 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7131639 11:99760120 T ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7104336 11:99760161 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7104336 11:99760161 T CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7104336 11:99760161 T CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7104336 11:99760161 T 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7104336 11:99760161 T CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7104336 11:99760161 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7104336 11:99760161 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7104336 11:99760161 T ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7120961 11:99760180 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7120961 11:99760180 T CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7120961 11:99760180 T CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7120961 11:99760180 T 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7120961 11:99760180 T CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7120961 11:99760180 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7120961 11:99760180 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7120961 11:99760180 T ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs7104369 11:99760231 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7104369 11:99760231 T CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7104369 11:99760231 T CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7104369 11:99760231 T 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7104369 11:99760231 T CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7104369 11:99760231 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7104369 11:99760231 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7104369 11:99760231 T ENSESTG00000008532 ENSESTT00000021465 Transcript intron_variant - - - - - - rs1218655 11:100032646 C 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs1218655 11:100032646 C ENSESTG00000008532 ENSESTT00000021499 Transcript intron_variant - - - - - - rs1218655 11:100032646 C CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs1218655 11:100032646 C CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs1218655 11:100032646 C 53942 NM_175566.2 Transcript intron_variant - - - - - - rs1218655 11:100032646 C CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs1218655 11:100032646 C 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs1218655 11:100032646 C ENSESTG00000008532 ENSESTT00000021504 Transcript intron_variant - - - - - - rs1218655 11:100032646 C 53942 NM_014361.3 Transcript intron_variant - - - - - - rs1218655 11:100032646 C ENSESTG00000008532 ENSESTT00000021515 Transcript intron_variant - - - - - - rs7930350 11:100074481 T 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs7930350 11:100074481 T ENSESTG00000008532 ENSESTT00000021499 Transcript intron_variant - - - - - - rs7930350 11:100074481 T CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs7930350 11:100074481 T CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs7930350 11:100074481 T 53942 NM_175566.2 Transcript intron_variant - - - - - - rs7930350 11:100074481 T CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs7930350 11:100074481 T 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs7930350 11:100074481 T ENSESTG00000008532 ENSESTT00000021504 Transcript intron_variant - - - - - - rs7930350 11:100074481 T 53942 NM_014361.3 Transcript intron_variant - - - - - - rs7930350 11:100074481 T ENSESTG00000008532 ENSESTT00000021515 Transcript intron_variant - - - - - - rs580605 11:100165851 C 53942 NM_001243270.1 Transcript intron_variant - - - - - - rs580605 11:100165851 C CCDS53696.1 CCDS53696.1 Transcript intron_variant - - - - - - rs580605 11:100165851 C CCDS58168.1 CCDS58168.1 Transcript intron_variant - - - - - - rs580605 11:100165851 C 53942 NM_175566.2 Transcript intron_variant - - - - - - rs580605 11:100165851 C CCDS53697.1 CCDS53697.1 Transcript intron_variant - - - - - - rs580605 11:100165851 C 53942 NM_001243271.1 Transcript intron_variant - - - - - - rs580605 11:100165851 C ENSESTG00000008532 ENSESTT00000021525 Transcript intron_variant - - - - - - rs580605 11:100165851 C 53942 NM_014361.3 Transcript intron_variant - - - - - - rs3016297 11:100470786 A - - - intergenic_variant - - - - - - rs1145424 11:100503445 A - - - intergenic_variant - - - - - - rs646392 11:100730213 A 143872 NM_152432.2 Transcript intron_variant - - - - - - rs646392 11:100730213 A ENSESTG00000021380 ENSESTT00000053723 Transcript intron_variant - - - - - - rs646392 11:100730213 A ENSESTG00000021380 ENSESTT00000053665 Transcript intron_variant - - - - - - rs646392 11:100730213 A ENSESTG00000021380 ENSESTT00000053718 Transcript intron_variant - - - - - - rs508856 11:100734069 G - ENSR00001572804 RegulatoryFeature regulatory_region_variant - - - - - - rs508856 11:100734069 G 143872 NM_152432.2 Transcript intron_variant - - - - - - rs508856 11:100734069 G ENSESTG00000021380 ENSESTT00000053723 Transcript intron_variant - - - - - - rs508856 11:100734069 G ENSESTG00000021380 ENSESTT00000053665 Transcript downstream_gene_variant - - - - - - DISTANCE=3729 rs508856 11:100734069 G ENSESTG00000021380 ENSESTT00000053718 Transcript intron_variant - - - - - - rs478287 11:100873249 C - - - intergenic_variant - - - - - - rs475623 11:100951459 C 5241 NM_000926.4 Transcript intron_variant - - - - - - rs475623 11:100951459 C ENSESTG00000022002 ENSESTT00000055438 Transcript intron_variant - - - - - - rs475623 11:100951459 C 5241 NM_001202474.1 Transcript intron_variant - - - - - - rs475623 11:100951459 C CCDS8310.1 CCDS8310.1 Transcript intron_variant - - - - - - rs475623 11:100951459 C ENSESTG00000022002 ENSESTT00000055455 Transcript intron_variant - - - - - - rs632787 11:100978479 A 5241 NM_000926.4 Transcript intron_variant - - - - - - rs632787 11:100978479 A ENSESTG00000022002 ENSESTT00000055365 Transcript intron_variant - - - - - - rs632787 11:100978479 A ENSESTG00000022002 ENSESTT00000055438 Transcript intron_variant - - - - - - rs632787 11:100978479 A 5241 NM_001202474.1 Transcript intron_variant - - - - - - rs632787 11:100978479 A CCDS8310.1 CCDS8310.1 Transcript intron_variant - - - - - - rs632787 11:100978479 A ENSESTG00000022002 ENSESTT00000055455 Transcript intron_variant - - - - - - rs10791471 11:101288670 G - - - intergenic_variant - - - - - - rs6590865 11:101355902 A CCDS8311.1 CCDS8311.1 Transcript intron_variant - - - - - - rs6590865 11:101355902 A 7225 NM_004621.5 Transcript intron_variant - - - - - - rs10750605 11:101378158 G ENSESTG00000021385 ENSESTT00000053654 Transcript intron_variant - - - - - - rs10750605 11:101378158 G CCDS8311.1 CCDS8311.1 Transcript intron_variant - - - - - - rs10750605 11:101378158 G 7225 NM_004621.5 Transcript intron_variant - - - - - - rs10750605 11:101378158 G ENSESTG00000021393 ENSESTT00000053680 Transcript upstream_gene_variant - - - - - - DISTANCE=2912 rs4754015 11:101443912 T ENSESTG00000021385 ENSESTT00000053654 Transcript intron_variant - - - - - - rs4754015 11:101443912 T CCDS8311.1 CCDS8311.1 Transcript intron_variant - - - - - - rs4754015 11:101443912 T 7225 NM_004621.5 Transcript intron_variant - - - - - - rs10791518 11:101565375 C - - - intergenic_variant - - - - - - rs1939032 11:101669087 G - - - intergenic_variant - - - - - - rs6590938 11:101814156 A ENSESTG00000020938 ENSESTT00000052550 Transcript intron_variant - - - - - - rs6590938 11:101814156 A CCDS31658.1 CCDS31658.1 Transcript intron_variant - - - - - - rs6590938 11:101814156 A ENSESTG00000020938 ENSESTT00000052618 Transcript upstream_gene_variant - - - - - - DISTANCE=4683 rs6590938 11:101814156 A ENSESTG00000020938 ENSESTT00000052603 Transcript upstream_gene_variant - - - - - - DISTANCE=950 rs6590938 11:101814156 A 57562 NM_020802.2 Transcript intron_variant - - - - - - rs6590938 11:101814156 A ENSESTG00000020938 ENSESTT00000052593 Transcript intron_variant - - - - - - rs6590939 11:101814186 A ENSESTG00000020938 ENSESTT00000052550 Transcript intron_variant - - - - - - rs6590939 11:101814186 A CCDS31658.1 CCDS31658.1 Transcript intron_variant - - - - - - rs6590939 11:101814186 A ENSESTG00000020938 ENSESTT00000052618 Transcript upstream_gene_variant - - - - - - DISTANCE=4653 rs6590939 11:101814186 A ENSESTG00000020938 ENSESTT00000052603 Transcript upstream_gene_variant - - - - - - DISTANCE=920 rs6590939 11:101814186 A 57562 NM_020802.2 Transcript intron_variant - - - - - - rs6590939 11:101814186 A ENSESTG00000020938 ENSESTT00000052593 Transcript intron_variant - - - - - - rs7926728 11:101832478 T - ENSR00001572844 RegulatoryFeature regulatory_region_variant - - - - - - rs7926728 11:101832478 T ENSESTG00000020979 ENSESTT00000052695 Transcript upstream_gene_variant - - - - - - DISTANCE=1107 rs7926728 11:101832478 T CCDS31658.1 CCDS31658.1 Transcript missense_variant 712 712 238 G/C Ggt/Tgt - PolyPhen=benign;SIFT=tolerated rs7926728 11:101832478 T ENSESTG00000020938 ENSESTT00000052622 Transcript missense_variant 276 115 39 G/C Ggt/Tgt - rs7926728 11:101832478 T 57562 NM_020802.2 Transcript missense_variant 982 712 238 G/C Ggt/Tgt - PolyPhen=benign;SIFT=tolerated rs7926728 11:101832478 T ENSESTG00000020938 ENSESTT00000052593 Transcript missense_variant 612 580 194 G/C Ggt/Tgt - rs9667568 11:102045341 A ENSESTG00000021331 ENSESTT00000053538 Transcript intron_variant - - - - - - rs9667568 11:102045341 A 10413 NM_001130145.2 Transcript intron_variant - - - - - - rs9667568 11:102045341 A CCDS53699.1 CCDS53699.1 Transcript intron_variant - - - - - - rs9667568 11:102045341 A CCDS44716.1 CCDS44716.1 Transcript intron_variant - - - - - - rs9667568 11:102045341 A 10413 NM_001195045.1 Transcript intron_variant - - - - - - rs9667568 11:102045341 A 10413 NM_006106.4 Transcript intron_variant - - - - - - rs9667568 11:102045341 A CCDS8314.2 CCDS8314.2 Transcript intron_variant - - - - - - rs9667568 11:102045341 A ENSESTG00000021090 ENSESTT00000052996 Transcript intron_variant - - - - - - rs9667568 11:102045341 A ENSESTG00000021090 ENSESTT00000052968 Transcript intron_variant - - - - - - rs9667568 11:102045341 A ENSESTG00000021090 ENSESTT00000053005 Transcript intron_variant - - - - - - rs9667568 11:102045341 A 10413 NM_001195044.1 Transcript intron_variant - - - - - - rs9667568 11:102045341 A CCDS53700.1 CCDS53700.1 Transcript intron_variant - - - - - - rs9667572 11:102045367 T ENSESTG00000021331 ENSESTT00000053538 Transcript intron_variant - - - - - - rs9667572 11:102045367 T 10413 NM_001130145.2 Transcript intron_variant - - - - - - rs9667572 11:102045367 T CCDS53699.1 CCDS53699.1 Transcript intron_variant - - - - - - rs9667572 11:102045367 T CCDS44716.1 CCDS44716.1 Transcript intron_variant - - - - - - rs9667572 11:102045367 T 10413 NM_001195045.1 Transcript intron_variant - - - - - - rs9667572 11:102045367 T 10413 NM_006106.4 Transcript intron_variant - - - - - - rs9667572 11:102045367 T CCDS8314.2 CCDS8314.2 Transcript intron_variant - - - - - - rs9667572 11:102045367 T ENSESTG00000021090 ENSESTT00000052996 Transcript intron_variant - - - - - - rs9667572 11:102045367 T ENSESTG00000021090 ENSESTT00000052968 Transcript intron_variant - - - - - - rs9667572 11:102045367 T ENSESTG00000021090 ENSESTT00000053005 Transcript intron_variant - - - - - - rs9667572 11:102045367 T 10413 NM_001195044.1 Transcript intron_variant - - - - - - rs9667572 11:102045367 T CCDS53700.1 CCDS53700.1 Transcript intron_variant - - - - - - rs4754838 11:102046400 C ENSESTG00000021331 ENSESTT00000053538 Transcript intron_variant - - - - - - rs4754838 11:102046400 C 10413 NM_001130145.2 Transcript intron_variant - - - - - - rs4754838 11:102046400 C CCDS53699.1 CCDS53699.1 Transcript intron_variant - - - - - - rs4754838 11:102046400 C CCDS44716.1 CCDS44716.1 Transcript intron_variant - - - - - - rs4754838 11:102046400 C 10413 NM_001195045.1 Transcript intron_variant - - - - - - rs4754838 11:102046400 C 10413 NM_006106.4 Transcript intron_variant - - - - - - rs4754838 11:102046400 C CCDS8314.2 CCDS8314.2 Transcript intron_variant - - - - - - rs4754838 11:102046400 C ENSESTG00000021090 ENSESTT00000052996 Transcript intron_variant - - - - - - rs4754838 11:102046400 C ENSESTG00000021090 ENSESTT00000052968 Transcript intron_variant - - - - - - rs4754838 11:102046400 C ENSESTG00000021090 ENSESTT00000053005 Transcript intron_variant - - - - - - rs4754838 11:102046400 C 10413 NM_001195044.1 Transcript intron_variant - - - - - - rs4754838 11:102046400 C CCDS53700.1 CCDS53700.1 Transcript intron_variant - - - - - - rs1298724 11:102134091 T ENSESTG00000021331 ENSESTT00000053538 Transcript intron_variant - - - - - - rs2445030 11:102239722 A CCDS58169.1 CCDS58169.1 Transcript intron_variant - - - - - - rs2445030 11:102239722 A 329 NM_001256163.1 Transcript intron_variant - - - - - - rs2445030 11:102239722 A CCDS8316.1 CCDS8316.1 Transcript intron_variant - - - - - - rs2445030 11:102239722 A ENSESTG00000021132 ENSESTT00000053030 Transcript intron_variant - - - - - - rs2445030 11:102239722 A 329 NM_001166.4 Transcript intron_variant - - - - - - rs2445030 11:102239722 A ENSESTG00000021272 ENSESTT00000053508 Transcript intron_variant - - - - - - rs2445030 11:102239722 A 329 NM_001256166.1 Transcript intron_variant - - - - - - rs2943219 11:103167527 T 79659 NM_001377.2 Transcript intron_variant - - - - - - rs2943219 11:103167527 T 79659 NM_001080463.1 Transcript intron_variant - - - - - - rs2943219 11:103167527 T ENSESTG00000030040 ENSESTT00000075961 Transcript intron_variant - - - - - - rs2943219 11:103167527 T CCDS53701.1 CCDS53701.1 Transcript intron_variant - - - - - - rs2943219 11:103167527 T ENSESTG00000030040 ENSESTT00000075948 Transcript intron_variant - - - - - - rs2943219 11:103167527 T CCDS44717.1 CCDS44717.1 Transcript intron_variant - - - - - - rs2512131 11:103182270 A 79659 NM_001377.2 Transcript intron_variant - - - - - - rs2512131 11:103182270 A 79659 NM_001080463.1 Transcript intron_variant - - - - - - rs2512131 11:103182270 A ENSESTG00000030040 ENSESTT00000075961 Transcript downstream_gene_variant - - - - - - DISTANCE=3710 rs2512131 11:103182270 A CCDS53701.1 CCDS53701.1 Transcript intron_variant - - - - - - rs2512131 11:103182270 A ENSESTG00000030282 ENSESTT00000076172 Transcript intron_variant - - - - - - rs2512131 11:103182270 A ENSESTG00000030040 ENSESTT00000075948 Transcript intron_variant - - - - - - rs2512131 11:103182270 A CCDS44717.1 CCDS44717.1 Transcript intron_variant - - - - - - rs2514420 11:103298008 C 79659 NM_001377.2 Transcript intron_variant - - - - - - rs2514420 11:103298008 C 79659 NM_001080463.1 Transcript intron_variant - - - - - - rs2514420 11:103298008 C CCDS53701.1 CCDS53701.1 Transcript intron_variant - - - - - - rs2514420 11:103298008 C ENSESTG00000030282 ENSESTT00000076172 Transcript intron_variant - - - - - - rs2514420 11:103298008 C ENSESTG00000030040 ENSESTT00000075981 Transcript intron_variant - - - - - - rs2514420 11:103298008 C ENSESTG00000030040 ENSESTT00000075948 Transcript intron_variant - - - - - - rs2514420 11:103298008 C CCDS44717.1 CCDS44717.1 Transcript intron_variant - - - - - - rs1481993 11:103454628 C - - - intergenic_variant - - - - - - rs1032236 11:103804003 A 80310 NM_033135.3 Transcript intron_variant - - - - - - rs1032236 11:103804003 A 80310 NM_025208.4 Transcript intron_variant - - - - - - rs1032236 11:103804003 A CCDS8326.1 CCDS8326.1 Transcript intron_variant - - - - - - rs1032236 11:103804003 A CCDS41703.1 CCDS41703.1 Transcript intron_variant - - - - - - rs361316 11:103924656 C 80310 NM_033135.3 Transcript intron_variant - - - - - - rs361316 11:103924656 C 80310 NM_025208.4 Transcript intron_variant - - - - - - rs361316 11:103924656 C ENSESTG00000007854 ENSESTT00000019847 Transcript intron_variant - - - - - - rs361316 11:103924656 C CCDS8326.1 CCDS8326.1 Transcript intron_variant - - - - - - rs361316 11:103924656 C CCDS41703.1 CCDS41703.1 Transcript intron_variant - - - - - - rs2515084 11:103974949 A 80310 NM_033135.3 Transcript intron_variant - - - - - - rs2515084 11:103974949 A 80310 NM_025208.4 Transcript intron_variant - - - - - - rs2515084 11:103974949 A ENSESTG00000007854 ENSESTT00000019847 Transcript intron_variant - - - - - - rs2515084 11:103974949 A CCDS8326.1 CCDS8326.1 Transcript intron_variant - - - - - - rs2515084 11:103974949 A CCDS41703.1 CCDS41703.1 Transcript intron_variant - - - - - - rs992892 11:104282181 A - - - intergenic_variant - - - - - - rs1552531 11:104289760 C - - - intergenic_variant - - - - - - rs7934643 11:104416710 T - - - intergenic_variant - - - - - - rs2408941 11:104423220 C - - - intergenic_variant - - - - - - rs1487699 11:104438692 T ENSESTG00000004346 ENSESTT00000010978 Transcript downstream_gene_variant - - - - - - DISTANCE=566 rs659367 11:104444764 A ENSESTG00000004346 ENSESTT00000010978 Transcript intron_variant - - - - - - rs1200616 11:104592793 T - - - intergenic_variant - - - - - - rs1147023 11:104597823 G - - - intergenic_variant - - - - - - rs76401094 11:104661470 A - - - intergenic_variant - - - - - - rs647039 11:104761206 T 100506742 NM_001191016.1 Transcript missense_variant 968 712 238 G/S Ggt/Agt - PolyPhen=benign;SIFT=tolerated rs647039 11:104761206 T CCDS55785.1 CCDS55785.1 Transcript missense_variant 712 712 238 G/S Ggt/Agt - PolyPhen=benign;SIFT=tolerated rs502825 11:104786072 G ENSESTG00000004339 ENSESTT00000010962 Transcript intron_variant - - - - - - rs502825 11:104786072 G ENSESTG00000004339 ENSESTT00000010968 Transcript intron_variant - - - - - - rs502825 11:104786072 G 643733 NR_034079.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs502825 11:104786072 G 643733 NR_034078.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs532190 11:104841352 A ENSESTG00000004309 ENSESTT00000010905 Transcript upstream_gene_variant - - - - - - DISTANCE=2047 rs532190 11:104841352 A ENSESTG00000004309 ENSESTT00000010908 Transcript upstream_gene_variant - - - - - - DISTANCE=2086 rs532190 11:104841352 A CCDS8327.1 CCDS8327.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2100 rs532190 11:104841352 A 837 NM_033306.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2093 rs532190 11:104841352 A 837 NM_001225.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2027 rs532190 11:104841352 A ENSESTG00000004309 ENSESTT00000010876 Transcript upstream_gene_variant - - - - - - DISTANCE=2031 rs2511327 11:104870190 G CCDS44718.1 CCDS44718.1 Transcript intron_variant - - - - - - rs2511327 11:104870190 G 838 NM_001136109.1 Transcript intron_variant - - - - - - rs2511327 11:104870190 G 838 NM_001136110.1 Transcript intron_variant - - - - - - rs2511327 11:104870190 G ENSESTG00000004298 ENSESTT00000010851 Transcript downstream_gene_variant - - - - - - DISTANCE=2564 rs2511327 11:104870190 G 838 NM_004347.3 Transcript intron_variant - - - - - - rs2511327 11:104870190 G ENSESTG00000004298 ENSESTT00000010845 Transcript intron_variant - - - - - - rs2511327 11:104870190 G CCDS44720.1 CCDS44720.1 Transcript intron_variant - - - - - - rs2511327 11:104870190 G 838 NM_001136112.1 Transcript intron_variant - - - - - - rs2511327 11:104870190 G 838 NR_036562.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2511327 11:104870190 G CCDS44719.1 CCDS44719.1 Transcript intron_variant - - - - - - rs2511327 11:104870190 G 838 NR_024239.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2511327 11:104870190 G CCDS8328.2 CCDS8328.2 Transcript intron_variant - - - - - - rs2509648 11:104896375 T 834 NM_001257119.1 Transcript 3_prime_UTR_variant 1806 - - - - - rs2509648 11:104896375 T 834 NM_001257118.1 Transcript 3_prime_UTR_variant 1869 - - - - - rs2509648 11:104896375 T CCDS8332.1 CCDS8332.1 Transcript downstream_gene_variant - - - - - - DISTANCE=610 rs2509648 11:104896375 T 834 NM_033292.3 Transcript intron_variant - - - - - - rs2509648 11:104896375 T ENSESTG00000004271 ENSESTT00000010800 Transcript downstream_gene_variant - - - - - - DISTANCE=4140 rs2509648 11:104896375 T ENSESTG00000004271 ENSESTT00000010760 Transcript downstream_gene_variant - - - - - - DISTANCE=4742 rs2509648 11:104896375 T 838 NM_001136112.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2480 rs2509648 11:104896375 T 838 NR_036562.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2480 rs2509648 11:104896375 T 838 NR_024239.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2480 rs2509648 11:104896375 T CCDS8328.2 CCDS8328.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2512 rs2509648 11:104896375 T 834 NM_001223.4 Transcript intron_variant - - - - - - rs2509648 11:104896375 T 838 NM_001136109.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2480 rs2509648 11:104896375 T CCDS44718.1 CCDS44718.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2512 rs2509648 11:104896375 T 838 NM_001136110.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2480 rs2509648 11:104896375 T CCDS8331.1 CCDS8331.1 Transcript downstream_gene_variant - - - - - - DISTANCE=610 rs2509648 11:104896375 T ENSESTG00000004298 ENSESTT00000010851 Transcript upstream_gene_variant - - - - - - DISTANCE=2480 rs2509648 11:104896375 T CCDS53704.1 CCDS53704.1 Transcript downstream_gene_variant - - - - - - DISTANCE=610 rs2509648 11:104896375 T 834 NM_033293.3 Transcript intron_variant - - - - - - rs2509648 11:104896375 T 834 NM_033294.3 Transcript intron_variant - - - - - - rs2509648 11:104896375 T CCDS8330.1 CCDS8330.1 Transcript downstream_gene_variant - - - - - - DISTANCE=610 rs2509648 11:104896375 T 834 NM_033295.3 Transcript intron_variant - - - - - - rs2509648 11:104896375 T 838 NM_004347.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2480 rs2509648 11:104896375 T ENSESTG00000004298 ENSESTT00000010845 Transcript upstream_gene_variant - - - - - - DISTANCE=2480 rs2509648 11:104896375 T CCDS44720.1 CCDS44720.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2512 rs2509648 11:104896375 T CCDS44719.1 CCDS44719.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2512 rs2509648 11:104896375 T ENSESTG00000004271 ENSESTT00000010779 Transcript downstream_gene_variant - - - - - - DISTANCE=4214 rs2509648 11:104896375 T CCDS8329.1 CCDS8329.1 Transcript downstream_gene_variant - - - - - - DISTANCE=610 rs2513257 11:105329319 A - - - intergenic_variant - - - - - - rs2513249 11:105335612 A - - - intergenic_variant - - - - - - rs7934375 11:105362644 G - - - intergenic_variant - - - - - - rs3133033 11:105447233 T - - - intergenic_variant - - - - - - rs7480412 11:105493884 T ENSESTG00000008080 ENSESTT00000020468 Transcript intron_variant - - - - - - rs7480412 11:105493884 T CCDS41707.1 CCDS41707.1 Transcript intron_variant - - - - - - rs7480412 11:105493884 T ENSESTG00000008080 ENSESTT00000020440 Transcript intron_variant - - - - - - rs7480412 11:105493884 T CCDS8333.1 CCDS8333.1 Transcript intron_variant - - - - - - rs7480412 11:105493884 T 2893 NM_001077243.2 Transcript intron_variant - - - - - - rs7480412 11:105493884 T 2893 NM_001077244.1 Transcript intron_variant - - - - - - rs7480412 11:105493884 T 2893 NM_001112812.1 Transcript intron_variant - - - - - - rs7480412 11:105493884 T 2893 NR_046356.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7480412 11:105493884 T CCDS41706.1 CCDS41706.1 Transcript intron_variant - - - - - - rs7480412 11:105493884 T 2893 NM_000829.3 Transcript intron_variant - - - - - - rs1269110 11:105559859 T ENSESTG00000008080 ENSESTT00000020468 Transcript intron_variant - - - - - - rs1269110 11:105559859 T CCDS41707.1 CCDS41707.1 Transcript intron_variant - - - - - - rs1269110 11:105559859 T ENSESTG00000008080 ENSESTT00000020440 Transcript intron_variant - - - - - - rs1269110 11:105559859 T CCDS8333.1 CCDS8333.1 Transcript intron_variant - - - - - - rs1269110 11:105559859 T 2893 NM_001077243.2 Transcript intron_variant - - - - - - rs1269110 11:105559859 T 2893 NM_001077244.1 Transcript intron_variant - - - - - - rs1269110 11:105559859 T 2893 NM_001112812.1 Transcript intron_variant - - - - - - rs1269110 11:105559859 T 2893 NR_046356.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1269110 11:105559859 T CCDS41706.1 CCDS41706.1 Transcript intron_variant - - - - - - rs1269110 11:105559859 T 2893 NM_000829.3 Transcript intron_variant - - - - - - rs1938962 11:105603969 C ENSESTG00000008080 ENSESTT00000020468 Transcript intron_variant - - - - - - rs1938962 11:105603969 C CCDS41707.1 CCDS41707.1 Transcript intron_variant - - - - - - rs1938962 11:105603969 C ENSESTG00000008080 ENSESTT00000020440 Transcript intron_variant - - - - - - rs1938962 11:105603969 C CCDS8333.1 CCDS8333.1 Transcript intron_variant - - - - - - rs1938962 11:105603969 C 2893 NM_001077243.2 Transcript intron_variant - - - - - - rs1938962 11:105603969 C 2893 NM_001077244.1 Transcript intron_variant - - - - - - rs1938962 11:105603969 C 2893 NM_001112812.1 Transcript intron_variant - - - - - - rs1938962 11:105603969 C 2893 NR_046356.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1938962 11:105603969 C CCDS41706.1 CCDS41706.1 Transcript intron_variant - - - - - - rs1938962 11:105603969 C 2893 NM_000829.3 Transcript intron_variant - - - - - - rs1271634 11:105737515 G CCDS41707.1 CCDS41707.1 Transcript intron_variant - - - - - - rs1271634 11:105737515 G CCDS8333.1 CCDS8333.1 Transcript intron_variant - - - - - - rs1271634 11:105737515 G 2893 NM_001077243.2 Transcript intron_variant - - - - - - rs1271634 11:105737515 G 2893 NM_001077244.1 Transcript intron_variant - - - - - - rs1271634 11:105737515 G 2893 NM_001112812.1 Transcript intron_variant - - - - - - rs1271634 11:105737515 G 2893 NR_046356.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1271634 11:105737515 G 2893 NM_000829.3 Transcript intron_variant - - - - - - rs1271634 11:105737515 G CCDS41706.1 CCDS41706.1 Transcript intron_variant - - - - - - rs655919 11:105769536 G ENSESTG00000008108 ENSESTT00000020504 Transcript intron_variant - - - - - - rs655919 11:105769536 G CCDS41707.1 CCDS41707.1 Transcript intron_variant - - - - - - rs655919 11:105769536 G CCDS8333.1 CCDS8333.1 Transcript intron_variant - - - - - - rs655919 11:105769536 G 2893 NM_001077243.2 Transcript intron_variant - - - - - - rs655919 11:105769536 G 2893 NM_001077244.1 Transcript intron_variant - - - - - - rs655919 11:105769536 G 2893 NM_001112812.1 Transcript intron_variant - - - - - - rs655919 11:105769536 G ENSESTG00000008108 ENSESTT00000020490 Transcript intron_variant - - - - - - rs655919 11:105769536 G 2893 NR_046356.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs655919 11:105769536 G ENSESTG00000008108 ENSESTT00000020505 Transcript intron_variant - - - - - - rs655919 11:105769536 G 2893 NM_000829.3 Transcript intron_variant - - - - - - rs655919 11:105769536 G CCDS41706.1 CCDS41706.1 Transcript intron_variant - - - - - - rs2435291 11:105905173 T - - - intergenic_variant - - - - - - rs7480362 11:105921333 A ENSESTG00000008182 ENSESTT00000020677 Transcript downstream_gene_variant - - - - - - DISTANCE=3627 rs7480362 11:105921333 A 143879 NM_152433.3 Transcript downstream_gene_variant - - - - - - DISTANCE=492 rs7480362 11:105921333 A ENSESTG00000008182 ENSESTT00000020686 Transcript downstream_gene_variant - - - - - - DISTANCE=3515 rs7480362 11:105921333 A 143879 NM_198439.2 Transcript downstream_gene_variant - - - - - - DISTANCE=492 rs7480362 11:105921333 A CCDS8334.1 CCDS8334.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2244 rs2458328 11:106289672 C - ENSR00001573109 RegulatoryFeature regulatory_region_variant - - - - - - rs2458328 11:106289672 C - - - intergenic_variant - - - - - - rs4475884 11:106833372 A CCDS58170.1 CCDS58170.1 Transcript intron_variant - - - - - - rs4475884 11:106833372 A 2977 NM_000855.2 Transcript intron_variant - - - - - - rs4475884 11:106833372 A 2977 NM_001256424.1 Transcript intron_variant - - - - - - rs4475884 11:106833372 A ENSESTG00000000417 ENSESTT00000001046 Transcript intron_variant - - - - - - rs4475884 11:106833372 A CCDS8335.1 CCDS8335.1 Transcript intron_variant - - - - - - rs2462429 11:106967129 A - - - intergenic_variant - - - - - - rs6588958 11:107153079 C - - - intergenic_variant - - - - - - rs4754211 11:107156307 T - - - intergenic_variant - - - - - - rs681453 11:107556132 G - - - intergenic_variant - - - - - - rs10736442 11:107879887 C - ENSR00000321375 RegulatoryFeature regulatory_region_variant - - - - - - rs10736442 11:107879887 C CCDS31668.1 CCDS31668.1 Transcript upstream_gene_variant - - - - - - DISTANCE=188 rs10736442 11:107879887 C ENSESTG00000002066 ENSESTT00000005178 Transcript 5_prime_UTR_variant 266 - - - - - rs10736442 11:107879887 C ENSESTG00000002066 ENSESTT00000005176 Transcript 5_prime_UTR_variant 266 - - - - - rs10736442 11:107879887 C ENSESTG00000002066 ENSESTT00000005180 Transcript 5_prime_UTR_variant 266 - - - - - rs10736442 11:107879887 C 8065 NM_003478.3 Transcript 5_prime_UTR_variant 480 - - - - - rs6589003 11:107985241 C ENSESTG00000002197 ENSESTT00000005498 Transcript intron_variant - - - - - - rs673308 11:108182097 A 472 NM_000051.3 Transcript intron_variant - - - - - - rs673308 11:108182097 A ENSESTG00000002158 ENSESTT00000005443 Transcript intron_variant - - - - - - rs673308 11:108182097 A ENSESTG00000002158 ENSESTT00000005450 Transcript intron_variant - - - - - - rs673308 11:108182097 A ENSESTG00000002158 ENSESTT00000005446 Transcript intron_variant - - - - - - rs673308 11:108182097 A CCDS31669.1 CCDS31669.1 Transcript intron_variant - - - - - - rs673308 11:108182097 A ENSESTG00000002158 ENSESTT00000005448 Transcript intron_variant - - - - - - rs659243 11:108183167 G 472 NM_000051.3 Transcript missense_variant 6333 5948 1983 N/S aAt/aGt - PolyPhen=benign;SIFT=tolerated rs659243 11:108183167 G ENSESTG00000002158 ENSESTT00000005443 Transcript missense_variant 234 224 75 N/S aAt/aGt - rs659243 11:108183167 G ENSESTG00000002158 ENSESTT00000005450 Transcript missense_variant 265 50 17 N/S aAt/aGt - rs659243 11:108183167 G ENSESTG00000002158 ENSESTT00000005446 Transcript missense_variant 234 224 75 N/S aAt/aGt - rs659243 11:108183167 G CCDS31669.1 CCDS31669.1 Transcript missense_variant 5948 5948 1983 N/S aAt/aGt - PolyPhen=benign;SIFT=tolerated rs659243 11:108183167 G ENSESTG00000002158 ENSESTT00000005448 Transcript missense_variant 234 224 75 N/S aAt/aGt - rs1943382 11:108380335 C 23086 NM_015065.2 Transcript missense_variant 6010 5899 1967 N/D Aat/Gat - PolyPhen=benign;SIFT=tolerated rs1943382 11:108380335 C CCDS8341.1 CCDS8341.1 Transcript missense_variant 5899 5899 1967 N/D Aat/Gat - PolyPhen=benign;SIFT=tolerated rs2846413 11:108401557 C ENSESTG00000030692 ENSESTT00000077282 Transcript intron_variant - - - - - - rs2846413 11:108401557 C ENSESTG00000030692 ENSESTT00000077252 Transcript intron_variant - - - - - - rs2846413 11:108401557 C ENSESTG00000030692 ENSESTT00000077261 Transcript intron_variant - - - - - - rs2846413 11:108401557 C ENSESTG00000030692 ENSESTT00000077269 Transcript intron_variant - - - - - - rs2846413 11:108401557 C 23086 NM_015065.2 Transcript intron_variant - - - - - - rs2846413 11:108401557 C CCDS8341.1 CCDS8341.1 Transcript intron_variant - - - - - - rs1791031 11:108485557 A - - - intergenic_variant - - - - - - rs1680531 11:108485568 A - - - intergenic_variant - - - - - - rs4754346 11:108556846 C 1662 NM_004398.2 Transcript intron_variant - - - - - - rs4754346 11:108556846 C ENSESTG00000030580 ENSESTT00000077212 Transcript intron_variant - - - - - - rs4754346 11:108556846 C CCDS8342.1 CCDS8342.1 Transcript intron_variant - - - - - - rs4754346 11:108556846 C ENSESTG00000030580 ENSESTT00000077188 Transcript intron_variant - - - - - - rs2615749 11:108623638 G 1662 NM_004398.2 Transcript intron_variant - - - - - - rs2615749 11:108623638 G ENSESTG00000030580 ENSESTT00000077212 Transcript intron_variant - - - - - - rs2615749 11:108623638 G CCDS8342.1 CCDS8342.1 Transcript intron_variant - - - - - - rs2615749 11:108623638 G ENSESTG00000030580 ENSESTT00000077188 Transcript intron_variant - - - - - - rs1469275 11:108771857 A ENSESTG00000030580 ENSESTT00000077227 Transcript intron_variant - - - - - - rs1469275 11:108771857 A 1662 NM_004398.2 Transcript intron_variant - - - - - - rs1469275 11:108771857 A ENSESTG00000030580 ENSESTT00000077212 Transcript intron_variant - - - - - - rs1469275 11:108771857 A ENSESTG00000030580 ENSESTT00000077237 Transcript intron_variant - - - - - - rs1469275 11:108771857 A CCDS8342.1 CCDS8342.1 Transcript intron_variant - - - - - - rs1469275 11:108771857 A ENSESTG00000030580 ENSESTT00000077188 Transcript intron_variant - - - - - - rs1509725 11:108909418 G - ENSR00001573285 RegulatoryFeature regulatory_region_variant - - - - - - rs1509725 11:108909418 G ENSESTG00000030707 ENSESTT00000077291 Transcript upstream_gene_variant - - - - - - DISTANCE=724 rs512212 11:109217943 A - - - intergenic_variant - - - - - - rs508300 11:109337636 T - - - intergenic_variant - - - - - - rs2852107 11:109600039 C - - - intergenic_variant - - - - - - rs2852133 11:109704607 C - - - intergenic_variant - - - - - - rs4576786 11:109814307 A - - - intergenic_variant - - - - - - rs4584543 11:109866925 T ENSESTG00000031140 ENSESTT00000078402 Transcript intron_variant - - - - - - rs625747 11:110053256 G 5962 NM_001260493.1 Transcript intron_variant - - - - - - rs2846739 11:110285329 A - - - intergenic_variant - - - - - - rs2724441 11:110314089 T CCDS8344.1 CCDS8344.1 Transcript intron_variant - - - - - - rs2724441 11:110314089 T ENSESTG00000024651 ENSESTT00000062400 Transcript intron_variant - - - - - - rs2724441 11:110314089 T 2230 NM_004109.4 Transcript intron_variant - - - - - - rs6589182 11:110726285 T - - - intergenic_variant - - - - - - rs7945775 11:110834076 G - ENSR00000568780 RegulatoryFeature regulatory_region_variant - - - - - - rs7945775 11:110834076 G - - - intergenic_variant - - - - - - rs10789814 11:111106618 T - - - intergenic_variant - - - - - - rs10789815 11:111106679 T - - - intergenic_variant - - - - - - rs10789816 11:111106698 T - - - intergenic_variant - - - - - - rs10891235 11:111106747 T - - - intergenic_variant - - - - - - rs10891236 11:111106766 T - - - intergenic_variant - - - - - - rs10891237 11:111106797 T - - - intergenic_variant - - - - - - rs10789818 11:111106848 T - - - intergenic_variant - - - - - - rs4938480 11:111212148 G - - - intergenic_variant - - - - - - rs3017768 11:111477430 T ENSESTG00000013311 ENSESTT00000033390 Transcript intron_variant - - - - - - rs3017768 11:111477430 T 23235 NM_015191.1 Transcript intron_variant - - - - - - rs3017768 11:111477430 T CCDS8347.1 CCDS8347.1 Transcript intron_variant - - - - - - rs524703 11:111602320 G - ENSR00000686252 RegulatoryFeature regulatory_region_variant - - - - - - rs524703 11:111602320 G ENSESTG00000013673 ENSESTT00000034260 Transcript intron_variant - - - - - - rs524703 11:111602320 G 5519 NM_181699.2 Transcript intron_variant - - - - - - rs524703 11:111602320 G ENSESTG00000013673 ENSESTT00000034275 Transcript intron_variant - - - - - - rs524703 11:111602320 G 23235 NM_015191.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4685 rs524703 11:111602320 G CCDS8348.1 CCDS8348.1 Transcript intron_variant - - - - - - rs524703 11:111602320 G CCDS53706.1 CCDS53706.1 Transcript intron_variant - - - - - - rs524703 11:111602320 G 5519 NM_181700.1 Transcript intron_variant - - - - - - rs524703 11:111602320 G ENSESTG00000013673 ENSESTT00000034269 Transcript intron_variant - - - - - - rs524703 11:111602320 G ENSESTG00000013330 ENSESTT00000033448 Transcript downstream_gene_variant - - - - - - DISTANCE=744 rs7112694 11:111627040 A ENSESTG00000013673 ENSESTT00000034260 Transcript intron_variant - - - - - - rs7112694 11:111627040 A 5519 NM_181699.2 Transcript intron_variant - - - - - - rs7112694 11:111627040 A ENSESTG00000013673 ENSESTT00000034275 Transcript intron_variant - - - - - - rs7112694 11:111627040 A CCDS8348.1 CCDS8348.1 Transcript intron_variant - - - - - - rs7112694 11:111627040 A 5519 NM_001177562.1 Transcript intron_variant - - - - - - rs7112694 11:111627040 A CCDS53706.1 CCDS53706.1 Transcript intron_variant - - - - - - rs7112694 11:111627040 A ENSESTG00000013673 ENSESTT00000034278 Transcript intron_variant - - - - - - rs7112694 11:111627040 A 5519 NM_181700.1 Transcript intron_variant - - - - - - rs7112694 11:111627040 A ENSESTG00000013673 ENSESTT00000034269 Transcript intron_variant - - - - - - rs7112694 11:111627040 A CCDS53707.1 CCDS53707.1 Transcript intron_variant - - - - - - rs7112694 11:111627040 A CCDS53708.1 CCDS53708.1 Transcript intron_variant - - - - - - rs7112694 11:111627040 A CCDS8349.1 CCDS8349.1 Transcript intron_variant - - - - - - rs7112694 11:111627040 A ENSESTG00000013673 ENSESTT00000034271 Transcript intron_variant - - - - - - rs7112694 11:111627040 A ENSESTG00000013673 ENSESTT00000034263 Transcript intron_variant - - - - - - rs7112694 11:111627040 A 5519 NM_001177563.1 Transcript intron_variant - - - - - - rs7112694 11:111627040 A 5519 NM_002716.4 Transcript intron_variant - - - - - - rs12420432 11:111783973 T - ENSR00001573490 RegulatoryFeature regulatory_region_variant - - - - - - rs12420432 11:111783973 T 3316 NM_001541.3 Transcript intron_variant - - - - - - rs12420432 11:111783973 T 1410 NM_001885.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1500 rs12420432 11:111783973 T CCDS8351.1 CCDS8351.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1525 rs12420432 11:111783973 T ENSESTG00000013580 ENSESTT00000033996 Transcript upstream_gene_variant - - - - - - DISTANCE=75 rs12420432 11:111783973 T ENSESTG00000013371 ENSESTT00000033513 Transcript intron_variant - - - - - - rs12420432 11:111783973 T CCDS8352.1 CCDS8352.1 Transcript intron_variant - - - - - - rs12420432 11:111783973 T ENSESTG00000013335 ENSESTT00000033467 Transcript downstream_gene_variant - - - - - - DISTANCE=1140 rs12420432 11:111783973 T 100528019 NR_037651.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs531227 11:111852167 G 85458 NM_033425.3 Transcript intron_variant - - - - - - rs531227 11:111852167 G ENSESTG00000013393 ENSESTT00000033569 Transcript intron_variant - - - - - - rs531227 11:111852167 G 85458 NM_001037954.2 Transcript intron_variant - - - - - - rs531227 11:111852167 G ENSESTG00000013393 ENSESTT00000033582 Transcript intron_variant - - - - - - rs10749987 11:111943434 A 55216 NM_001082969.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1534 rs10749987 11:111943434 A ENSESTG00000013571 ENSESTT00000033948 Transcript intron_variant - - - - - - rs10749987 11:111943434 A ENSESTG00000013467 ENSESTT00000033703 Transcript upstream_gene_variant - - - - - - DISTANCE=1600 rs10749987 11:111943434 A 55216 NM_001082970.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1534 rs10749987 11:111943434 A 120379 NM_138789.3 Transcript intron_variant - - - - - - rs10749987 11:111943434 A CCDS8356.2 CCDS8356.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2865 rs10749987 11:111943434 A ENSESTG00000013571 ENSESTT00000033955 Transcript intron_variant - - - - - - rs10749987 11:111943434 A ENSESTG00000013467 ENSESTT00000033710 Transcript upstream_gene_variant - - - - - - DISTANCE=1671 rs10749987 11:111943434 A ENSESTG00000013571 ENSESTT00000033968 Transcript intron_variant - - - - - - rs10749987 11:111943434 A CCDS8355.1 CCDS8355.1 Transcript intron_variant - - - - - - rs10749987 11:111943434 A 55216 NM_018195.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1534 rs10749987 11:111943434 A CCDS44730.1 CCDS44730.1 Transcript intron_variant - - - - - - rs10749987 11:111943434 A CCDS41715.1 CCDS41715.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2865 rs10749987 11:111943434 A 120379 NM_001082619.1 Transcript intron_variant - - - - - - rs10749987 11:111943434 A ENSESTG00000013571 ENSESTT00000033965 Transcript intron_variant - - - - - - rs2852377 11:111990836 G - ENSR00000568977 RegulatoryFeature regulatory_region_variant - - - - - - rs2852377 11:111990836 G - - - intergenic_variant - - - - - - rs2852374 11:111997149 T - - - intergenic_variant - - - - - - rs58408817 11:112125129 G 349633 NM_001145024.1 Transcript intron_variant - - - - - - rs4245075 11:112211093 A - - - intergenic_variant - - - - - - rs10749998 11:112393960 A ENSESTG00000008188 ENSESTT00000020685 Transcript intron_variant - - - - - - rs1892980 11:112842936 A ENSESTG00000008119 ENSESTT00000020537 Transcript intron_variant - - - - - - rs1892980 11:112842936 A 4684 NM_001242608.1 Transcript intron_variant - - - - - - rs1892980 11:112842936 A ENSESTG00000008119 ENSESTT00000020522 Transcript intron_variant - - - - - - rs1892980 11:112842936 A 4684 NM_001076682.3 Transcript intron_variant - - - - - - rs1892980 11:112842936 A 4684 NM_000615.6 Transcript intron_variant - - - - - - rs1892980 11:112842936 A 4684 NM_001242607.1 Transcript intron_variant - - - - - - rs1892980 11:112842936 A ENSESTG00000008119 ENSESTT00000020563 Transcript intron_variant - - - - - - rs1892980 11:112842936 A 4684 NM_181351.4 Transcript intron_variant - - - - - - rs7930957 11:112888049 A ENSESTG00000008119 ENSESTT00000020537 Transcript intron_variant - - - - - - rs7930957 11:112888049 A 4684 NM_001242608.1 Transcript intron_variant - - - - - - rs7930957 11:112888049 A ENSESTG00000008119 ENSESTT00000020522 Transcript intron_variant - - - - - - rs7930957 11:112888049 A 4684 NM_001076682.3 Transcript intron_variant - - - - - - rs7930957 11:112888049 A 4684 NM_000615.6 Transcript intron_variant - - - - - - rs7930957 11:112888049 A 4684 NM_001242607.1 Transcript intron_variant - - - - - - rs7930957 11:112888049 A ENSESTG00000008119 ENSESTT00000020563 Transcript intron_variant - - - - - - rs7930957 11:112888049 A 4684 NM_181351.4 Transcript intron_variant - - - - - - rs2186875 11:112943508 A ENSESTG00000008119 ENSESTT00000020537 Transcript intron_variant - - - - - - rs2186875 11:112943508 A 4684 NM_001242608.1 Transcript intron_variant - - - - - - rs2186875 11:112943508 A ENSESTG00000008119 ENSESTT00000020522 Transcript intron_variant - - - - - - rs2186875 11:112943508 A 4684 NM_001076682.3 Transcript intron_variant - - - - - - rs2186875 11:112943508 A 4684 NM_000615.6 Transcript intron_variant - - - - - - rs2186875 11:112943508 A 4684 NM_001242607.1 Transcript intron_variant - - - - - - rs2186875 11:112943508 A ENSESTG00000008119 ENSESTT00000020563 Transcript intron_variant - - - - - - rs2186875 11:112943508 A 4684 NM_181351.4 Transcript intron_variant - - - - - - rs2853193 11:112984100 A ENSESTG00000008119 ENSESTT00000020537 Transcript intron_variant - - - - - - rs2853193 11:112984100 A 4684 NM_001242608.1 Transcript intron_variant - - - - - - rs2853193 11:112984100 A ENSESTG00000008119 ENSESTT00000020522 Transcript intron_variant - - - - - - rs2853193 11:112984100 A 4684 NM_001076682.3 Transcript intron_variant - - - - - - rs2853193 11:112984100 A 4684 NM_000615.6 Transcript intron_variant - - - - - - rs2853193 11:112984100 A 4684 NM_001242607.1 Transcript intron_variant - - - - - - rs2853193 11:112984100 A ENSESTG00000008119 ENSESTT00000020563 Transcript intron_variant - - - - - - rs2853193 11:112984100 A 4684 NM_181351.4 Transcript intron_variant - - - - - - rs2846917 11:113004821 T ENSESTG00000008119 ENSESTT00000020537 Transcript intron_variant - - - - - - rs2846917 11:113004821 T 4684 NM_001242608.1 Transcript intron_variant - - - - - - rs2846917 11:113004821 T ENSESTG00000008119 ENSESTT00000020522 Transcript intron_variant - - - - - - rs2846917 11:113004821 T 4684 NM_001076682.3 Transcript intron_variant - - - - - - rs2846917 11:113004821 T 4684 NM_000615.6 Transcript intron_variant - - - - - - rs2846917 11:113004821 T 4684 NM_001242607.1 Transcript intron_variant - - - - - - rs2846917 11:113004821 T ENSESTG00000008119 ENSESTT00000020563 Transcript intron_variant - - - - - - rs2846917 11:113004821 T 4684 NM_181351.4 Transcript intron_variant - - - - - - rs654038 11:113093331 G ENSESTG00000008119 ENSESTT00000020537 Transcript intron_variant - - - - - - rs654038 11:113093331 G 4684 NM_001242608.1 Transcript intron_variant - - - - - - rs654038 11:113093331 G ENSESTG00000008119 ENSESTT00000020522 Transcript intron_variant - - - - - - rs654038 11:113093331 G 4684 NM_001076682.3 Transcript intron_variant - - - - - - rs654038 11:113093331 G ENSESTG00000008168 ENSESTT00000020630 Transcript intron_variant - - - - - - rs654038 11:113093331 G 4684 NM_000615.6 Transcript intron_variant - - - - - - rs654038 11:113093331 G 4684 NM_001242607.1 Transcript intron_variant - - - - - - rs654038 11:113093331 G 4684 NM_181351.4 Transcript intron_variant - - - - - - rs2850306 11:113173736 T ENSESTG00000008148 ENSESTT00000020574 Transcript intron_variant - - - - - - rs4612842 11:113629035 T CCDS8363.1 CCDS8363.1 Transcript intron_variant - - - - - - rs4612842 11:113629035 T ENSESTG00000001302 ENSESTT00000003096 Transcript intron_variant - - - - - - rs4612842 11:113629035 T 9183 NM_004724.3 Transcript intron_variant - - - - - - rs4612842 11:113629035 T ENSESTG00000001302 ENSESTT00000003091 Transcript intron_variant - - - - - - rs2428013 11:113708755 T CCDS31680.1 CCDS31680.1 Transcript intron_variant - - - - - - rs2428013 11:113708755 T ENSESTG00000001276 ENSESTT00000003051 Transcript downstream_gene_variant - - - - - - DISTANCE=2587 rs2428013 11:113708755 T 57646 NM_020886.2 Transcript intron_variant - - - - - - rs2428013 11:113708755 T ENSESTG00000001276 ENSESTT00000003031 Transcript intron_variant - - - - - - rs1784690 11:113839291 T - - - intergenic_variant - - - - - - rs612050 11:113986011 G ENSESTG00000001245 ENSESTT00000002957 Transcript intron_variant - - - - - - rs612050 11:113986011 G 7704 NM_001018011.1 Transcript intron_variant - - - - - - rs612050 11:113986011 G 7704 NM_006006.4 Transcript intron_variant - - - - - - rs612050 11:113986011 G CCDS8367.1 CCDS8367.1 Transcript intron_variant - - - - - - rs1712782 11:114603102 T - - - intergenic_variant - - - - - - rs10790052 11:114776182 A - - - intergenic_variant - - - - - - rs6589483 11:115060229 C ENSESTG00000029743 ENSESTT00000075005 Transcript intron_variant - - - - - - rs6589483 11:115060229 C CCDS8373.1 CCDS8373.1 Transcript intron_variant - - - - - - rs6589483 11:115060229 C ENSESTG00000029743 ENSESTT00000074973 Transcript intron_variant - - - - - - rs6589483 11:115060229 C ENSESTG00000029743 ENSESTT00000074961 Transcript intron_variant - - - - - - rs6589483 11:115060229 C CCDS53711.1 CCDS53711.1 Transcript intron_variant - - - - - - rs6589483 11:115060229 C 23705 NM_001098517.1 Transcript intron_variant - - - - - - rs6589483 11:115060229 C 23705 NM_014333.3 Transcript intron_variant - - - - - - rs6589483 11:115060229 C ENSESTG00000029743 ENSESTT00000075015 Transcript intron_variant - - - - - - rs6589483 11:115060229 C ENSESTG00000029743 ENSESTT00000075081 Transcript intron_variant - - - - - - rs6589483 11:115060229 C ENSESTG00000029743 ENSESTT00000075098 Transcript intron_variant - - - - - - rs6589483 11:115060229 C ENSESTG00000029743 ENSESTT00000075023 Transcript downstream_gene_variant - - - - - - DISTANCE=1100 rs6589483 11:115060229 C ENSESTG00000029743 ENSESTT00000075064 Transcript intron_variant - - - - - - rs1234498 11:115160647 C CCDS53711.1 CCDS53711.1 Transcript intron_variant - - - - - - rs1234498 11:115160647 C 23705 NM_001098517.1 Transcript intron_variant - - - - - - rs1234498 11:115160647 C 23705 NM_014333.3 Transcript intron_variant - - - - - - rs1234498 11:115160647 C CCDS8373.1 CCDS8373.1 Transcript intron_variant - - - - - - rs2027898 11:115214658 G CCDS53711.1 CCDS53711.1 Transcript intron_variant - - - - - - rs2027898 11:115214658 G 23705 NM_001098517.1 Transcript intron_variant - - - - - - rs2027898 11:115214658 G 23705 NM_014333.3 Transcript intron_variant - - - - - - rs2027898 11:115214658 G ENSESTG00000002226 ENSESTT00000005578 Transcript downstream_gene_variant - - - - - - DISTANCE=3678 rs2027898 11:115214658 G CCDS8373.1 CCDS8373.1 Transcript intron_variant - - - - - - rs2105981 11:115237569 C CCDS53711.1 CCDS53711.1 Transcript intron_variant - - - - - - rs2105981 11:115237569 C 23705 NM_001098517.1 Transcript intron_variant - - - - - - rs2105981 11:115237569 C 23705 NM_014333.3 Transcript intron_variant - - - - - - rs2105981 11:115237569 C CCDS8373.1 CCDS8373.1 Transcript intron_variant - - - - - - rs220851 11:115245392 C CCDS53711.1 CCDS53711.1 Transcript intron_variant - - - - - - rs220851 11:115245392 C 23705 NM_001098517.1 Transcript intron_variant - - - - - - rs220851 11:115245392 C 23705 NM_014333.3 Transcript intron_variant - - - - - - rs220851 11:115245392 C ENSESTG00000002272 ENSESTT00000005660 Transcript downstream_gene_variant - - - - - - DISTANCE=1801 rs220851 11:115245392 C CCDS8373.1 CCDS8373.1 Transcript intron_variant - - - - - - rs170224 11:115258033 A CCDS53711.1 CCDS53711.1 Transcript intron_variant - - - - - - rs170224 11:115258033 A 23705 NM_001098517.1 Transcript intron_variant - - - - - - rs170224 11:115258033 A 23705 NM_014333.3 Transcript intron_variant - - - - - - rs170224 11:115258033 A ENSESTG00000002272 ENSESTT00000005660 Transcript intron_variant - - - - - - rs170224 11:115258033 A CCDS8373.1 CCDS8373.1 Transcript intron_variant - - - - - - rs2427676 11:115274629 T ENSESTG00000002279 ENSESTT00000005671 Transcript intron_variant - - - - - - rs2427676 11:115274629 T CCDS53711.1 CCDS53711.1 Transcript intron_variant - - - - - - rs2427676 11:115274629 T 23705 NM_001098517.1 Transcript intron_variant - - - - - - rs2427676 11:115274629 T 23705 NM_014333.3 Transcript intron_variant - - - - - - rs2427676 11:115274629 T ENSESTG00000002272 ENSESTT00000005660 Transcript intron_variant - - - - - - rs2427676 11:115274629 T CCDS8373.1 CCDS8373.1 Transcript intron_variant - - - - - - rs220863 11:115296175 A ENSESTG00000002279 ENSESTT00000005671 Transcript intron_variant - - - - - - rs220863 11:115296175 A CCDS53711.1 CCDS53711.1 Transcript intron_variant - - - - - - rs220863 11:115296175 A 23705 NM_001098517.1 Transcript intron_variant - - - - - - rs220863 11:115296175 A ENSESTG00000002281 ENSESTT00000005678 Transcript upstream_gene_variant - - - - - - DISTANCE=4594 rs220863 11:115296175 A 23705 NM_014333.3 Transcript intron_variant - - - - - - rs220863 11:115296175 A ENSESTG00000002272 ENSESTT00000005660 Transcript intron_variant - - - - - - rs220863 11:115296175 A CCDS8373.1 CCDS8373.1 Transcript intron_variant - - - - - - rs2846906 11:115477731 C - ENSR00000569345 RegulatoryFeature regulatory_region_variant - - - - - - rs2846906 11:115477731 C - - - intergenic_variant - - - - - - rs2613466 11:115484403 T - - - intergenic_variant - - - - - - rs2846899 11:115486432 C - - - intergenic_variant - - - - - - rs1785018 11:115513281 C - - - intergenic_variant - - - - - - rs2515321 11:115513538 A - - - intergenic_variant - - - - - - rs1785014 11:115520881 C - - - intergenic_variant - - - - - - rs1785012 11:115522269 C - - - intergenic_variant - - - - - - rs1698184 11:115523685 G - - - intergenic_variant - - - - - - rs1698207 11:115526045 A ENSESTG00000002239 ENSESTT00000005599 Transcript upstream_gene_variant - - - - - - DISTANCE=3841 rs1785004 11:115531997 A ENSESTG00000002239 ENSESTT00000005599 Transcript intron_variant - - - - - - rs1785001 11:115534237 T ENSESTG00000002239 ENSESTT00000005599 Transcript intron_variant - - - - - - rs1784978 11:115550871 G ENSESTG00000002239 ENSESTT00000005599 Transcript intron_variant - - - - - - rs1698158 11:115572092 G ENSESTG00000002239 ENSESTT00000005599 Transcript intron_variant - - - - - - rs1784953 11:115574266 T ENSESTG00000002239 ENSESTT00000005599 Transcript intron_variant - - - - - - rs2512592 11:115585951 C ENSESTG00000002239 ENSESTT00000005599 Transcript intron_variant - - - - - - rs2512596 11:115697871 A ENSESTG00000002239 ENSESTT00000005599 Transcript intron_variant - - - - - - rs2508808 11:115698320 C ENSESTG00000002239 ENSESTT00000005599 Transcript intron_variant - - - - - - rs1939690 11:115743113 C - ENSR00000569382 RegulatoryFeature regulatory_region_variant - - - - - - rs1939690 11:115743113 C - - - intergenic_variant - - - - - - rs1530173 11:116168769 G - - - intergenic_variant - - - - - - rs920453 11:116180294 C - - - intergenic_variant - - - - - - rs540499 11:116210751 G - - - intergenic_variant - - - - - - rs483448 11:116224245 G - ENSR00000569433 RegulatoryFeature regulatory_region_variant - - - - - - rs483448 11:116224245 G - - - intergenic_variant - - - - - - rs1660077 11:116230442 G - - - intergenic_variant - - - - - - rs577176 11:116240536 G - - - intergenic_variant - - - - - - rs493119 11:116254697 T - - - intergenic_variant - - - - - - rs509101 11:116284150 T - - - intergenic_variant - - - - - - rs558243 11:116303494 A - - - intergenic_variant - - - - - - rs541643 11:116323148 C - - - intergenic_variant - - - - - - rs539765 11:117160347 G 23621 NM_138973.3 Transcript missense_variant 1695 1234 412 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G 23621 NM_001207048.1 Transcript missense_variant 1264 1141 381 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G CCDS55786.1 CCDS55786.1 Transcript missense_variant 1066 1066 356 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G 23621 NM_138971.3 Transcript missense_variant 1770 1309 437 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G 23621 NM_012104.4 Transcript missense_variant 1902 1441 481 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G CCDS55787.1 CCDS55787.1 Transcript missense_variant 1141 1141 381 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G CCDS44741.1 CCDS44741.1 Transcript missense_variant 1234 1234 412 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G CCDS8383.1 CCDS8383.1 Transcript missense_variant 1441 1441 481 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G ENSESTG00000018607 ENSESTT00000046938 Transcript downstream_gene_variant - - - - - - DISTANCE=3955 rs539765 11:117160347 G CCDS41720.1 CCDS41720.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4480 rs539765 11:117160347 G 257160 NM_207343.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3943 rs539765 11:117160347 G ENSESTG00000004691 ENSESTT00000011844 Transcript downstream_gene_variant - - - - - - DISTANCE=4156 rs539765 11:117160347 G 23621 NM_001207049.1 Transcript missense_variant 1189 1066 356 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G 257160 NM_001077239.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3943 rs539765 11:117160347 G 100379571 NR_037803.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1715 rs539765 11:117160347 G CCDS44740.1 CCDS44740.1 Transcript missense_variant 1309 1309 437 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G ENSESTG00000004917 ENSESTT00000012526 Transcript downstream_gene_variant - - - - - - DISTANCE=3472 rs539765 11:117160347 G CCDS44739.1 CCDS44739.1 Transcript missense_variant 1366 1366 456 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs539765 11:117160347 G 23621 NM_138972.3 Transcript missense_variant 1827 1366 456 C/R Tgc/Cgc - PolyPhen=benign;SIFT=tolerated rs948101 11:117622017 C CCDS8384.1 CCDS8384.1 Transcript intron_variant - - - - - - rs948101 11:117622017 C 57453 NM_020693.2 Transcript intron_variant - - - - - - rs2515801 11:117824705 C - - - intergenic_variant - - - - - - rs2512142 11:117893874 T 100526771 NR_038318.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10790253 11:118479723 C - ENSR00001574015 RegulatoryFeature regulatory_region_variant - - - - - - rs10790253 11:118479723 C ENSESTG00000027415 ENSESTT00000069135 Transcript upstream_gene_variant - - - - - - DISTANCE=862 rs10790253 11:118479723 C ENSESTG00000027415 ENSESTT00000069101 Transcript upstream_gene_variant - - - - - - DISTANCE=862 rs10790253 11:118479723 C 23187 NM_001144758.2 Transcript intron_variant - - - - - - rs10790253 11:118479723 C CCDS8401.1 CCDS8401.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4829 rs10790253 11:118479723 C 23187 NM_001144759.2 Transcript intron_variant - - - - - - rs10790253 11:118479723 C 23187 NM_015157.3 Transcript intron_variant - - - - - - rs10790253 11:118479723 C ENSESTG00000027375 ENSESTT00000068937 Transcript intron_variant - - - - - - rs10790253 11:118479723 C CCDS44750.1 CCDS44750.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4829 rs7106022 11:118553888 G - ENSR00001574022 RegulatoryFeature regulatory_region_variant - - - - - - rs7106022 11:118553888 G ENSESTG00000029053 ENSESTT00000073257 Transcript upstream_gene_variant - - - - - - DISTANCE=3529 rs7106022 11:118553888 G 11181 NM_007180.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3507 rs7106022 11:118553888 G ENSESTG00000029053 ENSESTT00000073262 Transcript upstream_gene_variant - - - - - - DISTANCE=3529 rs7106022 11:118553888 G ENSESTG00000029053 ENSESTT00000073162 Transcript upstream_gene_variant - - - - - - DISTANCE=3529 rs7121619 11:118586952 G - ENSR00000569789 RegulatoryFeature regulatory_region_variant - - - - - - rs7121619 11:118586952 G - - - intergenic_variant - - - - - - rs4938538 11:118606886 G - - - intergenic_variant - - - - - - rs6589693 11:118635011 A ENSESTG00000028956 ENSESTT00000073060 Transcript downstream_gene_variant - - - - - - DISTANCE=3730 rs6589693 11:118635011 A ENSESTG00000028956 ENSESTT00000073119 Transcript downstream_gene_variant - - - - - - DISTANCE=3730 rs6589693 11:118635011 A ENSESTG00000028956 ENSESTT00000073130 Transcript intron_variant - - - - - - rs6589693 11:118635011 A 1656 NM_004397.4 Transcript intron_variant - - - - - - rs6589693 11:118635011 A ENSESTG00000028956 ENSESTT00000073039 Transcript intron_variant - - - - - - rs6589693 11:118635011 A CCDS44751.1 CCDS44751.1 Transcript intron_variant - - - - - - rs6589693 11:118635011 A ENSESTG00000028956 ENSESTT00000073079 Transcript downstream_gene_variant - - - - - - DISTANCE=3832 rs6589693 11:118635011 A 1656 NM_001257191.1 Transcript intron_variant - - - - - - rs6589693 11:118635011 A ENSESTG00000028956 ENSESTT00000073104 Transcript intron_variant - - - - - - rs6589693 11:118635011 A ENSESTG00000028956 ENSESTT00000073111 Transcript downstream_gene_variant - - - - - - DISTANCE=3730 rs6589693 11:118635011 A ENSESTG00000028956 ENSESTT00000073070 Transcript downstream_gene_variant - - - - - - DISTANCE=3730 rs7124395 11:118639315 T ENSESTG00000028956 ENSESTT00000073060 Transcript intron_variant - - - - - - rs7124395 11:118639315 T ENSESTG00000028956 ENSESTT00000073119 Transcript intron_variant - - - - - - rs7124395 11:118639315 T ENSESTG00000028956 ENSESTT00000073130 Transcript intron_variant - - - - - - rs7124395 11:118639315 T 1656 NM_004397.4 Transcript intron_variant - - - - - - rs7124395 11:118639315 T ENSESTG00000028956 ENSESTT00000073039 Transcript intron_variant - - - - - - rs7124395 11:118639315 T CCDS44751.1 CCDS44751.1 Transcript intron_variant - - - - - - rs7124395 11:118639315 T ENSESTG00000028956 ENSESTT00000073079 Transcript intron_variant - - - - - - rs7124395 11:118639315 T 1656 NM_001257191.1 Transcript intron_variant - - - - - - rs7124395 11:118639315 T ENSESTG00000028956 ENSESTT00000073104 Transcript intron_variant - - - - - - rs7124395 11:118639315 T ENSESTG00000028956 ENSESTT00000073111 Transcript intron_variant - - - - - - rs7124395 11:118639315 T ENSESTG00000028956 ENSESTT00000073070 Transcript intron_variant - - - - - - rs7936347 11:118676980 G - - - intergenic_variant - - - - - - rs7927475 11:118681366 A - - - intergenic_variant - - - - - - rs4938548 11:118693276 C - ENSR00000569804 RegulatoryFeature regulatory_region_variant - - - - - - rs4938548 11:118693276 C - - - intergenic_variant - - - - - - rs10790279 11:118797990 C ENSESTG00000027696 ENSESTT00000069727 Transcript intron_variant - - - - - - rs4938622 11:118939774 C - ENSR00000321921 RegulatoryFeature regulatory_region_variant - - - - - - rs4938622 11:118939774 C 55823 NM_021729.4 Transcript intron_variant - - - - - - rs4938622 11:118939774 C ENSESTG00000027877 ENSESTT00000070352 Transcript upstream_gene_variant - - - - - - DISTANCE=4351 rs4938622 11:118939774 C ENSESTG00000027877 ENSESTT00000070320 Transcript intron_variant - - - - - - rs4938622 11:118939774 C ENSESTG00000027877 ENSESTT00000070340 Transcript upstream_gene_variant - - - - - - DISTANCE=1291 rs10790285 11:119038913 G - ENSR00000569863 RegulatoryFeature regulatory_region_variant - - - - - - rs10790285 11:119038913 G ENSESTG00000028338 ENSESTT00000071256 Transcript intron_variant - - - - - - rs10790285 11:119038913 G CCDS44752.1 CCDS44752.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3200 rs10790285 11:119038913 G ENSESTG00000028338 ENSESTT00000071384 Transcript upstream_gene_variant - - - - - - DISTANCE=552 rs10790285 11:119038913 G ENSESTG00000028338 ENSESTT00000071334 Transcript upstream_gene_variant - - - - - - DISTANCE=123 rs10790285 11:119038913 G ENSESTG00000028338 ENSESTT00000071350 Transcript upstream_gene_variant - - - - - - DISTANCE=509 rs10790285 11:119038913 G ENSESTG00000028338 ENSESTT00000071372 Transcript upstream_gene_variant - - - - - - DISTANCE=512 rs10790285 11:119038913 G ENSESTG00000028338 ENSESTT00000071398 Transcript upstream_gene_variant - - - - - - DISTANCE=595 rs10790285 11:119038913 G 79671 NM_170722.1 Transcript upstream_gene_variant - - - - - - DISTANCE=527 rs10790285 11:119038913 G 79671 NM_024618.2 Transcript upstream_gene_variant - - - - - - DISTANCE=527 rs10790285 11:119038913 G CCDS8416.1 CCDS8416.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3200 rs7945501 11:119062525 A 283152 NM_001145018.1 Transcript intron_variant - - - - - - rs7945501 11:119062525 A ENSESTG00000028455 ENSESTT00000071560 Transcript downstream_gene_variant - - - - - - DISTANCE=3720 rs7945501 11:119062525 A ENSESTG00000028455 ENSESTT00000071647 Transcript downstream_gene_variant - - - - - - DISTANCE=3679 rs7945501 11:119062525 A 79849 NM_001168468.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1593 rs7945501 11:119062525 A ENSESTG00000028455 ENSESTT00000071582 Transcript downstream_gene_variant - - - - - - DISTANCE=3786 rs7945501 11:119062525 A CCDS44753.1 CCDS44753.1 Transcript intron_variant - - - - - - rs7945501 11:119062525 A CCDS8417.1 CCDS8417.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2324 rs7945501 11:119062525 A CCDS53719.1 CCDS53719.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2324 rs7945501 11:119062525 A 79849 NR_033122.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1593 rs7945501 11:119062525 A ENSESTG00000028513 ENSESTT00000071668 Transcript downstream_gene_variant - - - - - - DISTANCE=1870 rs7945501 11:119062525 A ENSESTG00000028538 ENSESTT00000071754 Transcript intron_variant - - - - - - rs7945501 11:119062525 A 79849 NM_024791.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1593 rs7945501 11:119062525 A ENSESTG00000028455 ENSESTT00000071608 Transcript downstream_gene_variant - - - - - - DISTANCE=3964 rs6589733 11:119186335 C - ENSR00000321960 RegulatoryFeature regulatory_region_variant - - - - - - rs6589733 11:119186335 C ENSESTG00000005897 ENSESTT00000015002 Transcript intron_variant - - - - - - rs6589733 11:119186335 C ENSESTG00000005897 ENSESTT00000015006 Transcript intron_variant - - - - - - rs6589733 11:119186335 C 4162 NM_006500.2 Transcript intron_variant - - - - - - rs6589733 11:119186335 C ENSESTG00000005897 ENSESTT00000014968 Transcript intron_variant - - - - - - rs6589733 11:119186335 C ENSESTG00000005897 ENSESTT00000014961 Transcript intron_variant - - - - - - rs6589733 11:119186335 C ENSESTG00000005897 ENSESTT00000014958 Transcript intron_variant - - - - - - rs6589733 11:119186335 C CCDS31690.1 CCDS31690.1 Transcript intron_variant - - - - - - rs682006 11:119254066 A 9099 NM_004205.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1630 rs682006 11:119254066 A 100499227 NR_034160.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs682006 11:119254066 A ENSESTG00000005721 ENSESTT00000014501 Transcript downstream_gene_variant - - - - - - DISTANCE=1743 rs682006 11:119254066 A ENSESTG00000005861 ENSESTT00000014870 Transcript upstream_gene_variant - - - - - - DISTANCE=1684 rs682006 11:119254066 A ENSESTG00000005861 ENSESTT00000014879 Transcript upstream_gene_variant - - - - - - DISTANCE=4241 rs682006 11:119254066 A 9099 NM_001243759.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1630 rs682006 11:119254066 A ENSESTG00000005861 ENSESTT00000014864 Transcript upstream_gene_variant - - - - - - DISTANCE=1652 rs682006 11:119254066 A CCDS58189.1 CCDS58189.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1839 rs7102145 11:119330489 G 100499227 NR_034160.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7396975 11:119342538 G ENSESTG00000005734 ENSESTT00000014521 Transcript intron_variant - - - - - - rs7396975 11:119342538 G 100499227 NR_034160.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10892370 11:119354682 C ENSESTG00000005734 ENSESTT00000014521 Transcript intron_variant - - - - - - rs10892370 11:119354682 C 100499227 NR_034160.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6589754 11:119373512 T ENSESTG00000005734 ENSESTT00000014521 Transcript downstream_gene_variant - - - - - - DISTANCE=3036 rs6589754 11:119373512 T 100499227 NR_034160.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3568 rs1465597 11:119373961 G ENSESTG00000005734 ENSESTT00000014521 Transcript downstream_gene_variant - - - - - - DISTANCE=3485 rs1465597 11:119373961 G 100499227 NR_034160.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4017 rs7479141 11:119376406 A - - - intergenic_variant - - - - - - rs591766 11:119385079 C - - - intergenic_variant - - - - - - rs7123669 11:119399194 G ENSESTG00000005738 ENSESTT00000014524 Transcript downstream_gene_variant - - - - - - DISTANCE=1820 rs4936480 11:119443831 G - ENSR00000686411 RegulatoryFeature regulatory_region_variant - - - - - - rs4936480 11:119443831 G - - - intergenic_variant - - - - - - rs6589765 11:119476755 C - - - intergenic_variant - - - - - - rs10790326 11:119500414 T ENSESTG00000005845 ENSESTT00000014815 Transcript intron_variant - - - - - - rs4459317 11:119538474 C ENSESTG00000005831 ENSESTT00000014801 Transcript downstream_gene_variant - - - - - - DISTANCE=4328 rs4459317 11:119538474 C CCDS8426.1 CCDS8426.1 Transcript intron_variant - - - - - - rs4459317 11:119538474 C 5818 NM_002855.4 Transcript intron_variant - - - - - - rs4459317 11:119538474 C ENSESTG00000005831 ENSESTT00000014800 Transcript intron_variant - - - - - - rs4459317 11:119538474 C CCDS8425.1 CCDS8425.1 Transcript intron_variant - - - - - - rs4459317 11:119538474 C 5818 NM_203285.1 Transcript intron_variant - - - - - - rs7119668 11:119656809 A - - - intergenic_variant - - - - - - rs6421574 11:119668021 G - - - intergenic_variant - - - - - - rs7937306 11:119683924 A - - - intergenic_variant - - - - - - rs4408322 11:120200382 T CCDS55792.1 CCDS55792.1 Transcript intron_variant - - - - - - rs4408322 11:120200382 T ENSESTG00000028030 ENSESTT00000070566 Transcript intron_variant - - - - - - rs4408322 11:120200382 T 219902 NM_174926.2 Transcript intron_variant - - - - - - rs4408322 11:120200382 T 219902 NM_001198671.1 Transcript intron_variant - - - - - - rs4408322 11:120200382 T 219902 NM_001198672.1 Transcript intron_variant - - - - - - rs4408322 11:120200382 T ENSESTG00000028030 ENSESTT00000070573 Transcript intron_variant - - - - - - rs4408322 11:120200382 T 219902 NM_001198673.1 Transcript intron_variant - - - - - - rs4408322 11:120200382 T 219902 NM_001198674.1 Transcript intron_variant - - - - - - rs4408322 11:120200382 T CCDS55793.1 CCDS55793.1 Transcript intron_variant - - - - - - rs4408322 11:120200382 T 219902 NM_001198675.1 Transcript intron_variant - - - - - - rs4408322 11:120200382 T CCDS8432.1 CCDS8432.1 Transcript intron_variant - - - - - - rs4408322 11:120200382 T 219902 NM_001198670.1 Transcript intron_variant - - - - - - rs642228 11:120833722 C ENSESTG00000028284 ENSESTT00000071125 Transcript downstream_gene_variant - - - - - - DISTANCE=2055 rs642228 11:120833722 C CCDS8433.1 CCDS8433.1 Transcript intron_variant - - - - - - rs642228 11:120833722 C 2900 NM_014619.2 Transcript intron_variant - - - - - - rs642228 11:120833722 C ENSESTG00000028379 ENSESTT00000071358 Transcript upstream_gene_variant - - - - - - DISTANCE=4984 rs602682 11:121003810 T 7007 NM_005422.2 Transcript intron_variant - - - - - - rs602682 11:121003810 T ENSESTG00000028349 ENSESTT00000071279 Transcript upstream_gene_variant - - - - - - DISTANCE=4437 rs602682 11:121003810 T CCDS8434.1 CCDS8434.1 Transcript intron_variant - - - - - - rs493269 11:121014282 C ENSESTG00000028359 ENSESTT00000071310 Transcript upstream_gene_variant - - - - - - DISTANCE=2362 rs493269 11:121014282 C 7007 NM_005422.2 Transcript intron_variant - - - - - - rs493269 11:121014282 C ENSESTG00000028349 ENSESTT00000071279 Transcript intron_variant - - - - - - rs493269 11:121014282 C CCDS8434.1 CCDS8434.1 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053831 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053970 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053920 Transcript intron_variant - - - - - - rs1784929 11:121475798 A 6653 NM_003105.5 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053882 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053938 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053861 Transcript intron_variant - - - - - - rs1784929 11:121475798 A CCDS8436.1 CCDS8436.1 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053699 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053878 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053865 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053962 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053928 Transcript intron_variant - - - - - - rs1784929 11:121475798 A ENSESTG00000021058 ENSESTT00000053914 Transcript intron_variant - - - - - - rs7120897 11:121599220 A - - - intergenic_variant - - - - - - rs7126205 11:122609211 G ENSESTG00000031925 ENSESTT00000080578 Transcript intron_variant - - - - - - rs7126205 11:122609211 G 84959 NM_032873.4 Transcript intron_variant - - - - - - rs7126205 11:122609211 G CCDS31694.1 CCDS31694.1 Transcript intron_variant - - - - - - rs1894083 11:122679736 T 84959 NM_032873.4 Transcript intron_variant - - - - - - rs1894083 11:122679736 T CCDS31694.1 CCDS31694.1 Transcript intron_variant - - - - - - rs3133257 11:123538194 A ENSESTG00000024405 ENSESTT00000061702 Transcript upstream_gene_variant - - - - - - DISTANCE=1013 rs6590008 11:123667436 A - - - intergenic_variant - - - - - - rs10893099 11:123754844 C 338661 NM_001013743.1 Transcript missense_variant 609 401 134 N/S aAt/aGt - PolyPhen=benign;SIFT=tolerated rs10893099 11:123754844 C CCDS31697.1 CCDS31697.1 Transcript missense_variant 401 401 134 N/S aAt/aGt - PolyPhen=benign;SIFT=tolerated rs1939849 11:123984666 A ENSESTG00000024412 ENSESTT00000061810 Transcript upstream_gene_variant - - - - - - DISTANCE=1496 rs1939849 11:123984666 A ENSESTG00000024412 ENSESTT00000061826 Transcript upstream_gene_variant - - - - - - DISTANCE=1496 rs1939849 11:123984666 A ENSESTG00000024412 ENSESTT00000061845 Transcript upstream_gene_variant - - - - - - DISTANCE=3534 rs1939849 11:123984666 A 4013 NM_198315.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1445 rs1939849 11:123984666 A CCDS8444.1 CCDS8444.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3553 rs1939849 11:123984666 A 4013 NM_014622.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1445 rs1939849 11:123984666 A CCDS8445.1 CCDS8445.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3553 rs1939849 11:123984666 A 4013 NM_001130142.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1445 rs10790636 11:124005912 T 4013 NM_014622.4 Transcript intron_variant - - - - - - rs10790636 11:124005912 T 4013 NM_001130142.1 Transcript intron_variant - - - - - - rs10790636 11:124005912 T ENSESTG00000024473 ENSESTT00000062075 Transcript intron_variant - - - - - - rs10790636 11:124005912 T CCDS8444.1 CCDS8444.1 Transcript intron_variant - - - - - - rs1939854 11:124028286 T - - - intergenic_variant - - - - - - rs2919476 11:125024691 G ENSESTG00000016043 ENSESTT00000040221 Transcript downstream_gene_variant - - - - - - DISTANCE=3666 rs1783928 11:125348435 G CCDS31716.1 CCDS31716.1 Transcript intron_variant - - - - - - rs1783928 11:125348435 G 9638 NM_005103.4 Transcript intron_variant - - - - - - rs1783928 11:125348435 G ENSESTG00000009811 ENSESTT00000024601 Transcript intron_variant - - - - - - rs1783928 11:125348435 G ENSESTG00000009811 ENSESTT00000024588 Transcript intron_variant - - - - - - rs1784214 11:125496956 T - ENSR00001574609 RegulatoryFeature regulatory_region_variant - - - - - - rs1784214 11:125496956 T 1111 NR_045204.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1784214 11:125496956 T ENSESTG00000009654 ENSESTT00000024223 Transcript intron_variant - - - - - - rs1784214 11:125496956 T 1111 NM_001114122.2 Transcript intron_variant - - - - - - rs1784214 11:125496956 T 1111 NR_045205.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1784214 11:125496956 T 1111 NM_001114121.2 Transcript intron_variant - - - - - - rs1784214 11:125496956 T ENSESTG00000009654 ENSESTT00000024237 Transcript intron_variant - - - - - - rs1784214 11:125496956 T 1111 NM_001244846.1 Transcript intron_variant - - - - - - rs1784214 11:125496956 T 1111 NM_001274.5 Transcript intron_variant - - - - - - rs1784214 11:125496956 T CCDS58191.1 CCDS58191.1 Transcript intron_variant - - - - - - rs1784214 11:125496956 T CCDS8459.1 CCDS8459.1 Transcript intron_variant - - - - - - rs1784214 11:125496956 T ENSESTG00000009654 ENSESTT00000024217 Transcript intron_variant - - - - - - rs2471472 11:125836826 A CCDS58192.1 CCDS58192.1 Transcript intron_variant - - - - - - rs2471472 11:125836826 A CCDS8468.1 CCDS8468.1 Transcript intron_variant - - - - - - rs2471472 11:125836826 A 50937 NM_016952.4 Transcript intron_variant - - - - - - rs2471472 11:125836826 A 50937 NM_001243597.1 Transcript intron_variant - - - - - - rs3016296 11:126479951 A CCDS55796.1 CCDS55796.1 Transcript intron_variant - - - - - - rs3016296 11:126479951 A 84623 NM_001161707.1 Transcript intron_variant - - - - - - rs3016296 11:126479951 A ENSESTG00000027262 ENSESTT00000068665 Transcript intron_variant - - - - - - rs3016296 11:126479951 A CCDS53723.1 CCDS53723.1 Transcript intron_variant - - - - - - rs3016296 11:126479951 A 84623 NM_032531.3 Transcript intron_variant - - - - - - rs515275 11:126513633 T CCDS55796.1 CCDS55796.1 Transcript intron_variant - - - - - - rs515275 11:126513633 T 84623 NM_001161707.1 Transcript intron_variant - - - - - - rs515275 11:126513633 T CCDS53723.1 CCDS53723.1 Transcript intron_variant - - - - - - rs515275 11:126513633 T 84623 NM_032531.3 Transcript intron_variant - - - - - - rs4935991 11:126660431 A - ENSR00001574697 RegulatoryFeature regulatory_region_variant - - - - - - rs4935991 11:126660431 A CCDS55796.1 CCDS55796.1 Transcript intron_variant - - - - - - rs4935991 11:126660431 A 84623 NM_001161707.1 Transcript intron_variant - - - - - - rs4935991 11:126660431 A CCDS53723.1 CCDS53723.1 Transcript intron_variant - - - - - - rs4935991 11:126660431 A 84623 NM_032531.3 Transcript intron_variant - - - - - - rs1784334 11:126832994 A CCDS55796.1 CCDS55796.1 Transcript intron_variant - - - - - - rs1784334 11:126832994 A 84623 NM_001161707.1 Transcript intron_variant - - - - - - rs1784334 11:126832994 A CCDS53723.1 CCDS53723.1 Transcript intron_variant - - - - - - rs1784334 11:126832994 A 84623 NM_032531.3 Transcript intron_variant - - - - - - rs7950589 11:126982106 T - - - intergenic_variant - - - - - - rs2510712 11:127020978 G - - - intergenic_variant - - - - - - rs3109103 11:127141136 T - - - intergenic_variant - - - - - - rs356257 11:127444666 G - - - intergenic_variant - - - - - - rs7945876 11:127771715 A - - - intergenic_variant - - - - - - rs485351 11:127845261 A - - - intergenic_variant - - - - - - rs4936042 11:128097083 T ENSESTG00000011941 ENSESTT00000029936 Transcript intron_variant - - - - - - rs4936042 11:128097083 T ENSESTG00000011941 ENSESTT00000029938 Transcript intron_variant - - - - - - rs592375 11:128544696 C - - - intergenic_variant - - - - - - rs694165 11:128724422 A ENSESTG00000012009 ENSESTT00000030099 Transcript intron_variant - - - - - - rs694165 11:128724422 A 3758 NM_153766.1 Transcript intron_variant - - - - - - rs694165 11:128724422 A 3758 NM_153765.1 Transcript intron_variant - - - - - - rs694165 11:128724422 A 3758 NM_153764.1 Transcript intron_variant - - - - - - rs694165 11:128724422 A 3758 NM_153767.2 Transcript intron_variant - - - - - - rs592796 11:128728613 G ENSESTG00000012009 ENSESTT00000030099 Transcript intron_variant - - - - - - rs592796 11:128728613 G 3758 NM_153766.1 Transcript intron_variant - - - - - - rs592796 11:128728613 G 3758 NM_153765.1 Transcript intron_variant - - - - - - rs592796 11:128728613 G 3758 NM_153764.1 Transcript intron_variant - - - - - - rs592796 11:128728613 G 3758 NM_153767.2 Transcript intron_variant - - - - - - rs2509822 11:128854419 T CCDS44769.1 CCDS44769.1 Transcript intron_variant - - - - - - rs2509822 11:128854419 T ENSESTG00000011993 ENSESTT00000030073 Transcript downstream_gene_variant - - - - - - DISTANCE=1994 rs2509822 11:128854419 T 9743 NM_001142685.1 Transcript intron_variant - - - - - - rs2509822 11:128854419 T CCDS31718.1 CCDS31718.1 Transcript intron_variant - - - - - - rs2509822 11:128854419 T 9743 NM_014715.3 Transcript intron_variant - - - - - - rs2509822 11:128854419 T ENSESTG00000011993 ENSESTT00000030071 Transcript downstream_gene_variant - - - - - - DISTANCE=1507 rs2509822 11:128854419 T ENSESTG00000011993 ENSESTT00000030077 Transcript downstream_gene_variant - - - - - - DISTANCE=1994 rs2509822 11:128854419 T ENSESTG00000011993 ENSESTT00000030084 Transcript downstream_gene_variant - - - - - - DISTANCE=2098 rs2509822 11:128854419 T ENSESTG00000011993 ENSESTT00000030075 Transcript downstream_gene_variant - - - - - - DISTANCE=1507 rs1786459 11:128866356 T CCDS44769.1 CCDS44769.1 Transcript intron_variant - - - - - - rs1786459 11:128866356 T ENSESTG00000011993 ENSESTT00000030073 Transcript intron_variant - - - - - - rs1786459 11:128866356 T 9743 NM_001142685.1 Transcript intron_variant - - - - - - rs1786459 11:128866356 T CCDS31718.1 CCDS31718.1 Transcript intron_variant - - - - - - rs1786459 11:128866356 T 9743 NM_014715.3 Transcript intron_variant - - - - - - rs1786459 11:128866356 T ENSESTG00000011993 ENSESTT00000030071 Transcript intron_variant - - - - - - rs1786459 11:128866356 T ENSESTG00000011993 ENSESTT00000030077 Transcript intron_variant - - - - - - rs1786459 11:128866356 T ENSESTG00000011993 ENSESTT00000030084 Transcript intron_variant - - - - - - rs1786459 11:128866356 T ENSESTG00000011993 ENSESTT00000030075 Transcript intron_variant - - - - - - rs4381383 11:128896344 A CCDS44769.1 CCDS44769.1 Transcript intron_variant - - - - - - rs4381383 11:128896344 A ENSESTG00000011993 ENSESTT00000030073 Transcript intron_variant - - - - - - rs4381383 11:128896344 A 9743 NM_001142685.1 Transcript intron_variant - - - - - - rs4381383 11:128896344 A 9743 NM_014715.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2256 rs4381383 11:128896344 A ENSESTG00000011993 ENSESTT00000030071 Transcript intron_variant - - - - - - rs4381383 11:128896344 A ENSESTG00000011993 ENSESTT00000030077 Transcript intron_variant - - - - - - rs4381383 11:128896344 A ENSESTG00000011993 ENSESTT00000030084 Transcript upstream_gene_variant - - - - - - DISTANCE=2209 rs4381383 11:128896344 A ENSESTG00000011993 ENSESTT00000030075 Transcript intron_variant - - - - - - rs2055074 11:129415829 G - - - intergenic_variant - - - - - - rs7484163 11:129537231 C - - - intergenic_variant - - - - - - rs1647970 11:130880814 C - ENSR00000571554 RegulatoryFeature regulatory_region_variant - - - - - - rs1647970 11:130880814 C - - - intergenic_variant - - - - - - rs3018390 11:130944871 T - - - intergenic_variant - - - - - - rs1793839 11:131180342 T - - - intergenic_variant - - - - - - rs2187574 11:131204689 C - - - intergenic_variant - - - - - - rs2458772 11:131437996 T 50863 NM_001048209.1 Transcript intron_variant - - - - - - rs2458772 11:131437996 T CCDS41733.1 CCDS41733.1 Transcript intron_variant - - - - - - rs906163 11:131494322 A 50863 NM_001048209.1 Transcript intron_variant - - - - - - rs906163 11:131494322 A CCDS41733.1 CCDS41733.1 Transcript intron_variant - - - - - - rs6590620 11:131958488 C - ENSR00000571666 RegulatoryFeature regulatory_region_variant - - - - - - rs6590620 11:131958488 C CCDS44778.1 CCDS44778.1 Transcript intron_variant - - - - - - rs6590620 11:131958488 C 50863 NM_001048209.1 Transcript intron_variant - - - - - - rs6590620 11:131958488 C 50863 NM_001144058.1 Transcript intron_variant - - - - - - rs6590620 11:131958488 C 50863 NM_016522.2 Transcript intron_variant - - - - - - rs6590620 11:131958488 C 50863 NM_001144059.1 Transcript intron_variant - - - - - - rs6590620 11:131958488 C CCDS8491.1 CCDS8491.1 Transcript intron_variant - - - - - - rs6590620 11:131958488 C CCDS44777.1 CCDS44777.1 Transcript intron_variant - - - - - - rs6590620 11:131958488 C CCDS41733.1 CCDS41733.1 Transcript intron_variant - - - - - - rs6590622 11:131968565 A CCDS44778.1 CCDS44778.1 Transcript intron_variant - - - - - - rs6590622 11:131968565 A 50863 NM_001048209.1 Transcript intron_variant - - - - - - rs6590622 11:131968565 A 50863 NM_001144058.1 Transcript intron_variant - - - - - - rs6590622 11:131968565 A 50863 NM_016522.2 Transcript intron_variant - - - - - - rs6590622 11:131968565 A 50863 NM_001144059.1 Transcript intron_variant - - - - - - rs6590622 11:131968565 A CCDS8491.1 CCDS8491.1 Transcript intron_variant - - - - - - rs6590622 11:131968565 A CCDS44777.1 CCDS44777.1 Transcript intron_variant - - - - - - rs6590622 11:131968565 A CCDS41733.1 CCDS41733.1 Transcript intron_variant - - - - - - rs6590626 11:132012060 C - ENSR00000571681 RegulatoryFeature regulatory_region_variant - - - - - - rs6590626 11:132012060 C ENSESTG00000009070 ENSESTT00000022761 Transcript intron_variant - - - - - - rs6590626 11:132012060 C CCDS44778.1 CCDS44778.1 Transcript intron_variant - - - - - - rs6590626 11:132012060 C 50863 NM_001048209.1 Transcript intron_variant - - - - - - rs6590626 11:132012060 C 50863 NM_001144058.1 Transcript intron_variant - - - - - - rs6590626 11:132012060 C 50863 NM_016522.2 Transcript intron_variant - - - - - - rs6590626 11:132012060 C 50863 NM_001144059.1 Transcript intron_variant - - - - - - rs6590626 11:132012060 C ENSESTG00000009064 ENSESTT00000022749 Transcript upstream_gene_variant - - - - - - DISTANCE=4219 rs6590626 11:132012060 C CCDS8491.1 CCDS8491.1 Transcript intron_variant - - - - - - rs6590626 11:132012060 C CCDS44777.1 CCDS44777.1 Transcript intron_variant - - - - - - rs6590626 11:132012060 C CCDS41733.1 CCDS41733.1 Transcript intron_variant - - - - - - rs586298 11:132309235 C ENSESTG00000005559 ENSESTT00000014198 Transcript intron_variant - - - - - - rs586298 11:132309235 C ENSESTG00000005559 ENSESTT00000014208 Transcript intron_variant - - - - - - rs586298 11:132309235 C ENSESTG00000005559 ENSESTT00000014227 Transcript intron_variant - - - - - - rs586298 11:132309235 C 4978 NM_001012393.1 Transcript intron_variant - - - - - - rs586298 11:132309235 C CCDS31722.1 CCDS31722.1 Transcript intron_variant - - - - - - rs586298 11:132309235 C 4978 NM_002545.3 Transcript intron_variant - - - - - - rs586298 11:132309235 C ENSESTG00000005559 ENSESTT00000014190 Transcript intron_variant - - - - - - rs586298 11:132309235 C CCDS8492.1 CCDS8492.1 Transcript intron_variant - - - - - - rs631784 11:132378387 T ENSESTG00000005559 ENSESTT00000014198 Transcript intron_variant - - - - - - rs631784 11:132378387 T ENSESTG00000005559 ENSESTT00000014208 Transcript intron_variant - - - - - - rs631784 11:132378387 T ENSESTG00000005559 ENSESTT00000014227 Transcript intron_variant - - - - - - rs631784 11:132378387 T 4978 NM_001012393.1 Transcript intron_variant - - - - - - rs631784 11:132378387 T CCDS31722.1 CCDS31722.1 Transcript intron_variant - - - - - - rs631784 11:132378387 T ENSESTG00000005601 ENSESTT00000014232 Transcript intron_variant - - - - - - rs631784 11:132378387 T 4978 NM_002545.3 Transcript intron_variant - - - - - - rs631784 11:132378387 T ENSESTG00000005559 ENSESTT00000014190 Transcript intron_variant - - - - - - rs631784 11:132378387 T CCDS8492.1 CCDS8492.1 Transcript intron_variant - - - - - - rs665582 11:132383417 T ENSESTG00000005559 ENSESTT00000014198 Transcript intron_variant - - - - - - rs665582 11:132383417 T ENSESTG00000005559 ENSESTT00000014208 Transcript intron_variant - - - - - - rs665582 11:132383417 T ENSESTG00000005559 ENSESTT00000014227 Transcript intron_variant - - - - - - rs665582 11:132383417 T 4978 NM_001012393.1 Transcript intron_variant - - - - - - rs665582 11:132383417 T CCDS31722.1 CCDS31722.1 Transcript intron_variant - - - - - - rs665582 11:132383417 T ENSESTG00000005601 ENSESTT00000014232 Transcript upstream_gene_variant - - - - - - DISTANCE=111 rs665582 11:132383417 T 4978 NM_002545.3 Transcript intron_variant - - - - - - rs665582 11:132383417 T ENSESTG00000005559 ENSESTT00000014190 Transcript intron_variant - - - - - - rs665582 11:132383417 T CCDS8492.1 CCDS8492.1 Transcript intron_variant - - - - - - rs7482909 11:132939978 G 4978 NM_001012393.1 Transcript intron_variant - - - - - - rs7482909 11:132939978 G CCDS31722.1 CCDS31722.1 Transcript intron_variant - - - - - - rs4245114 11:133214279 T - ENSR00001575213 RegulatoryFeature regulatory_region_variant - - - - - - rs4245114 11:133214279 T 4978 NM_001012393.1 Transcript intron_variant - - - - - - rs4245114 11:133214279 T CCDS31722.1 CCDS31722.1 Transcript intron_variant - - - - - - rs6590711 11:133343911 A 4978 NM_001012393.1 Transcript intron_variant - - - - - - rs6590711 11:133343911 A CCDS31722.1 CCDS31722.1 Transcript intron_variant - - - - - - rs1982922 11:133623898 C - - - intergenic_variant - - - - - - rs645423 11:133828142 C - ENSR00001575225 RegulatoryFeature regulatory_region_variant - - - - - - rs645423 11:133828142 C 22997 NM_014987.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1262 rs1259021 11:134105165 G ENSESTG00000003320 ENSESTT00000008318 Transcript upstream_gene_variant - - - - - - DISTANCE=4380 rs1259021 11:134105165 G ENSESTG00000003320 ENSESTT00000008310 Transcript intron_variant - - - - - - rs1259021 11:134105165 G ENSESTG00000003320 ENSESTT00000008305 Transcript intron_variant - - - - - - rs1259021 11:134105165 G 112936 NM_052875.3 Transcript intron_variant - - - - - - rs1259021 11:134105165 G CCDS8495.1 CCDS8495.1 Transcript intron_variant - - - - - - rs1259021 11:134105165 G ENSESTG00000003320 ENSESTT00000008301 Transcript intron_variant - - - - - - rs6590747 11:134416864 T - - - intergenic_variant - - - - - - rs1018202 11:134739395 T - - - intergenic_variant - - - - - - rs10791400 11:134746845 G - - - intergenic_variant - - - - - - rs4980936 12:647277 T - ENSR00000424957 RegulatoryFeature regulatory_region_variant - - - - - - rs4980936 12:647277 T 283358 NM_173593.3 Transcript intron_variant - - - - - - rs4980936 12:647277 T CCDS8504.1 CCDS8504.1 Transcript intron_variant - - - - - - rs4980936 12:647277 T ENSESTG00000024912 ENSESTT00000063245 Transcript intron_variant - - - - - - rs4980936 12:647277 T ENSESTG00000024912 ENSESTT00000063275 Transcript intron_variant - - - - - - rs4980936 12:647277 T ENSESTG00000024912 ENSESTT00000063301 Transcript intron_variant - - - - - - rs7957649 12:860595 C - ENSR00001460684 RegulatoryFeature regulatory_region_variant - - - - - - rs7957649 12:860595 C - MA0139.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=13;MOTIF_NAME=Jaspar_Matrix_CTCF:MA0139.1;HIGH_INF_POS=Y;MOTIF_SCORE_CHANGE=0.060 rs7957649 12:860595 C CCDS8506.1 CCDS8506.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2137 rs7957649 12:860595 C ENSESTG00000025220 ENSESTT00000063722 Transcript upstream_gene_variant - - - - - - DISTANCE=2691 rs7957649 12:860595 C CCDS53731.1 CCDS53731.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2137 rs7957649 12:860595 C 65125 NM_213655.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1494 rs7957649 12:860595 C 65125 NM_018979.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1494 rs7957649 12:860595 C 65125 NM_001184985.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1494 rs7957649 12:860595 C 65125 NM_014823.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1494 rs7310044 12:1440627 T 23085 NR_027946.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7310044 12:1440627 T CCDS53732.1 CCDS53732.1 Transcript intron_variant - - - - - - rs7310044 12:1440627 T 23085 NM_178040.2 Transcript intron_variant - - - - - - rs7310044 12:1440627 T 23085 NR_027949.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7310044 12:1440627 T ENSESTG00000008528 ENSESTT00000021459 Transcript intron_variant - - - - - - rs7310044 12:1440627 T ENSESTG00000008528 ENSESTT00000021471 Transcript intron_variant - - - - - - rs7310044 12:1440627 T 23085 NR_027948.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7310044 12:1440627 T CCDS8508.1 CCDS8508.1 Transcript intron_variant - - - - - - rs7310044 12:1440627 T 23085 NM_178039.2 Transcript intron_variant - - - - - - rs886539 12:1578138 T 23085 NR_027946.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs886539 12:1578138 T CCDS53732.1 CCDS53732.1 Transcript intron_variant - - - - - - rs886539 12:1578138 T 23085 NM_178040.2 Transcript intron_variant - - - - - - rs886539 12:1578138 T 23085 NR_027949.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs886539 12:1578138 T 23085 NR_027948.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs886539 12:1578138 T CCDS8508.1 CCDS8508.1 Transcript intron_variant - - - - - - rs886539 12:1578138 T ENSESTG00000008528 ENSESTT00000021511 Transcript intron_variant - - - - - - rs886539 12:1578138 T 23085 NM_178039.2 Transcript intron_variant - - - - - - rs2470394 12:1999298 C CCDS44785.1 CCDS44785.1 Transcript intron_variant - - - - - - rs2470394 12:1999298 C 93589 NM_172364.4 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44800.1 CCDS44800.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44788.1 CCDS44788.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129843.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44798.1 CCDS44798.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_000719.6 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_199460.2 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129833.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS53734.1 CCDS53734.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS53735.1 CCDS53735.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129839.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44790.1 CCDS44790.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129835.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129831.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129842.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129844.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44787.1 CCDS44787.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129846.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS53733.1 CCDS53733.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129841.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001167624.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129836.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129830.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44791.1 CCDS44791.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129837.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129827.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44795.1 CCDS44795.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44799.1 CCDS44799.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44793.1 CCDS44793.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44794.1 CCDS44794.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44796.1 CCDS44796.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44792.1 CCDS44792.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44801.1 CCDS44801.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129834.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44789.1 CCDS44789.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS44797.1 CCDS44797.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129832.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001167625.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C CCDS53736.1 CCDS53736.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129829.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001167623.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129838.1 Transcript intron_variant - - - - - - rs4765664 12:2255349 C 775 NM_001129840.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44800.1 CCDS44800.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44788.1 CCDS44788.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129843.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44798.1 CCDS44798.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_000719.6 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_199460.2 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129833.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS53734.1 CCDS53734.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS53735.1 CCDS53735.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129839.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44790.1 CCDS44790.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129835.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129831.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129842.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129844.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44787.1 CCDS44787.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129846.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS53733.1 CCDS53733.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129841.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 100874234 NR_046578.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4978 rs7958331 12:2324725 C 775 NM_001167624.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129836.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129830.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44791.1 CCDS44791.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129837.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129827.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44795.1 CCDS44795.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44799.1 CCDS44799.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44793.1 CCDS44793.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44794.1 CCDS44794.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44796.1 CCDS44796.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44792.1 CCDS44792.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44801.1 CCDS44801.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129834.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44789.1 CCDS44789.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS44797.1 CCDS44797.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129832.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001167625.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C CCDS53736.1 CCDS53736.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129829.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001167623.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129838.1 Transcript intron_variant - - - - - - rs7958331 12:2324725 C 775 NM_001129840.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44800.1 CCDS44800.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44788.1 CCDS44788.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129843.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44798.1 CCDS44798.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G ENSESTG00000028778 ENSESTT00000072507 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_000719.6 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_199460.2 Transcript missense_variant 5991 5678 1893 K/R aAa/aGa - rs10774054 12:2791205 G 775 NM_001129833.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS53734.1 CCDS53734.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS53735.1 CCDS53735.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129839.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44790.1 CCDS44790.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129835.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129831.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 100652846 NR_045725.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129842.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129844.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44787.1 CCDS44787.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129846.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS53733.1 CCDS53733.1 Transcript missense_variant 5534 5534 1845 K/R aAa/aGa - PolyPhen=unknown;SIFT=tolerated rs10774054 12:2791205 G 775 NM_001129841.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001167624.1 Transcript missense_variant 5847 5534 1845 K/R aAa/aGa - PolyPhen=unknown;SIFT=tolerated rs10774054 12:2791205 G 775 NM_001129836.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129830.1 Transcript missense_variant 5847 5534 1845 K/R aAa/aGa - PolyPhen=unknown;SIFT=tolerated rs10774054 12:2791205 G CCDS44791.1 CCDS44791.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129837.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129827.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44795.1 CCDS44795.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44799.1 CCDS44799.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44793.1 CCDS44793.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44794.1 CCDS44794.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44796.1 CCDS44796.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44792.1 CCDS44792.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44801.1 CCDS44801.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129834.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44789.1 CCDS44789.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS44797.1 CCDS44797.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129832.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001167625.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G CCDS53736.1 CCDS53736.1 Transcript missense_variant 5534 5534 1845 K/R aAa/aGa - PolyPhen=unknown;SIFT=tolerated rs10774054 12:2791205 G 775 NM_001129829.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G ENSESTG00000029379 ENSESTT00000073958 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001167623.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G ENSESTG00000028778 ENSESTT00000072522 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129838.1 Transcript intron_variant - - - - - - rs10774054 12:2791205 G 775 NM_001129840.1 Transcript intron_variant - - - - - - rs2058216 12:2894787 C ENSESTG00000029370 ENSESTT00000073927 Transcript downstream_gene_variant - - - - - - DISTANCE=1743 rs2058216 12:2894787 C ENSESTG00000029241 ENSESTT00000073665 Transcript intron_variant - - - - - - rs7976357 12:3029595 C ENSESTG00000015947 ENSESTT00000040040 Transcript intron_variant - - - - - - rs7976357 12:3029595 C ENSESTG00000015947 ENSESTT00000040016 Transcript intron_variant - - - - - - rs7976357 12:3029595 C CCDS53737.1 CCDS53737.1 Transcript intron_variant - - - - - - rs7976357 12:3029595 C 7289 NM_003324.4 Transcript intron_variant - - - - - - rs7976357 12:3029595 C 7289 NM_001160408.1 Transcript intron_variant - - - - - - rs7976357 12:3029595 C CCDS8519.1 CCDS8519.1 Transcript intron_variant - - - - - - rs7976357 12:3029595 C ENSESTG00000029071 ENSESTT00000073314 Transcript intron_variant - - - - - - rs7976357 12:3029595 C ENSESTG00000015947 ENSESTT00000040022 Transcript intron_variant - - - - - - rs7976357 12:3029595 C ENSESTG00000029071 ENSESTT00000073341 Transcript intron_variant - - - - - - rs7976357 12:3029595 C ENSESTG00000015947 ENSESTT00000040054 Transcript intron_variant - - - - - - rs7976357 12:3029595 C ENSESTG00000015947 ENSESTT00000040046 Transcript intron_variant - - - - - - rs7972731 12:3257146 C 10867 NM_001168320.1 Transcript intron_variant - - - - - - rs7972731 12:3257146 C ENSESTG00000016030 ENSESTT00000040226 Transcript intron_variant - - - - - - rs7972731 12:3257146 C 10867 NM_006675.4 Transcript intron_variant - - - - - - rs7980618 12:3332696 G 10867 NM_001168320.1 Transcript intron_variant - - - - - - rs7980618 12:3332696 G CCDS8520.1 CCDS8520.1 Transcript intron_variant - - - - - - rs7980618 12:3332696 G ENSESTG00000016030 ENSESTT00000040226 Transcript intron_variant - - - - - - rs7980618 12:3332696 G 10867 NM_006675.4 Transcript intron_variant - - - - - - rs7980618 12:3332696 G ENSESTG00000016030 ENSESTT00000040241 Transcript intron_variant - - - - - - rs10848859 12:3457094 G - - - intergenic_variant - - - - - - rs4766114 12:3522989 A ENSESTG00000016072 ENSESTT00000040303 Transcript intron_variant - - - - - - rs4766114 12:3522989 A ENSESTG00000016072 ENSESTT00000040288 Transcript intron_variant - - - - - - rs4766114 12:3522989 A 56341 NM_001256536.1 Transcript intron_variant - - - - - - rs4766114 12:3522989 A CCDS58200.1 CCDS58200.1 Transcript intron_variant - - - - - - rs6489487 12:3715399 G - - - intergenic_variant - - - - - - rs4765745 12:3729517 A 84766 NM_001144958.1 Transcript intron_variant - - - - - - rs4765745 12:3729517 A CCDS44803.1 CCDS44803.1 Transcript intron_variant - - - - - - rs242038 12:3780297 G 84766 NM_001144958.1 Transcript intron_variant - - - - - - rs242038 12:3780297 G CCDS8522.1 CCDS8522.1 Transcript intron_variant - - - - - - rs242038 12:3780297 G 84766 NM_032680.3 Transcript intron_variant - - - - - - rs242038 12:3780297 G ENSESTG00000016130 ENSESTT00000040465 Transcript intron_variant - - - - - - rs242038 12:3780297 G CCDS44803.1 CCDS44803.1 Transcript intron_variant - - - - - - rs242007 12:3803600 T 84766 NM_001144958.1 Transcript intron_variant - - - - - - rs242007 12:3803600 T CCDS8522.1 CCDS8522.1 Transcript intron_variant - - - - - - rs242007 12:3803600 T 84766 NM_032680.3 Transcript intron_variant - - - - - - rs242007 12:3803600 T ENSESTG00000016119 ENSESTT00000040442 Transcript intron_variant - - - - - - rs242007 12:3803600 T CCDS44803.1 CCDS44803.1 Transcript intron_variant - - - - - - rs6489531 12:4381763 G - ENSR00000425517 RegulatoryFeature regulatory_region_variant - - - - - - rs6489531 12:4381763 G CCDS8524.1 CCDS8524.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1444 rs6489531 12:4381763 G ENSESTG00000017774 ENSESTT00000044763 Transcript intron_variant - - - - - - rs6489531 12:4381763 G ENSESTG00000017767 ENSESTT00000044753 Transcript intron_variant - - - - - - rs6489531 12:4381763 G ENSESTG00000017759 ENSESTT00000044736 Transcript downstream_gene_variant - - - - - - DISTANCE=1201 rs6489531 12:4381763 G 894 NM_001759.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1139 rs6489531 12:4381763 G ENSESTG00000017260 ENSESTT00000043392 Transcript upstream_gene_variant - - - - - - DISTANCE=1200 rs7962720 12:4668862 T ENSESTG00000017357 ENSESTT00000043722 Transcript upstream_gene_variant - - - - - - DISTANCE=2518 rs7962720 12:4668862 T CCDS8529.1 CCDS8529.1 Transcript downstream_gene_variant - - - - - - DISTANCE=703 rs7962720 12:4668862 T CCDS44805.1 CCDS44805.1 Transcript downstream_gene_variant - - - - - - DISTANCE=703 rs7962720 12:4668862 T ENSESTG00000017317 ENSESTT00000043607 Transcript 3_prime_UTR_variant 1747 - - - - - rs7962720 12:4668862 T ENSESTG00000017357 ENSESTT00000043707 Transcript upstream_gene_variant - - - - - - DISTANCE=2518 rs7962720 12:4668862 T 10635 NM_006479.4 Transcript 3_prime_UTR_variant 1867 - - - - - rs7962720 12:4668862 T 10635 NM_001130862.1 Transcript 3_prime_UTR_variant 1918 - - - - - rs7962720 12:4668862 T ENSESTG00000017357 ENSESTT00000043651 Transcript upstream_gene_variant - - - - - - DISTANCE=2514 rs2109098 12:4815933 A - - - intergenic_variant - - - - - - rs6489610 12:5275494 C - - - intergenic_variant - - - - - - rs6489614 12:5349617 A ENSESTG00000031663 ENSESTT00000079887 Transcript upstream_gene_variant - - - - - - DISTANCE=2197 rs6489614 12:5349617 A ENSESTG00000031663 ENSESTT00000079865 Transcript intron_variant - - - - - - rs6489614 12:5349617 A ENSESTG00000031663 ENSESTT00000079899 Transcript upstream_gene_variant - - - - - - DISTANCE=2201 rs6489614 12:5349617 A ENSESTG00000031663 ENSESTT00000079884 Transcript upstream_gene_variant - - - - - - DISTANCE=426 rs6489614 12:5349617 A ENSESTG00000031663 ENSESTT00000079876 Transcript upstream_gene_variant - - - - - - DISTANCE=348 rs993026 12:5350131 A ENSESTG00000031663 ENSESTT00000079887 Transcript upstream_gene_variant - - - - - - DISTANCE=2711 rs993026 12:5350131 A ENSESTG00000031663 ENSESTT00000079865 Transcript intron_variant - - - - - - rs993026 12:5350131 A ENSESTG00000031663 ENSESTT00000079899 Transcript upstream_gene_variant - - - - - - DISTANCE=2715 rs993026 12:5350131 A ENSESTG00000031663 ENSESTT00000079884 Transcript upstream_gene_variant - - - - - - DISTANCE=940 rs993026 12:5350131 A ENSESTG00000031663 ENSESTT00000079876 Transcript upstream_gene_variant - - - - - - DISTANCE=862 rs1978390 12:5559894 T 4908 NM_001102654.1 Transcript intron_variant - - - - - - rs1978390 12:5559894 T ENSESTG00000031516 ENSESTT00000079493 Transcript intron_variant - - - - - - rs1978390 12:5559894 T CCDS44806.1 CCDS44806.1 Transcript intron_variant - - - - - - rs1978390 12:5559894 T ENSESTG00000031516 ENSESTT00000079509 Transcript intron_variant - - - - - - rs10744686 12:5669792 T ENSESTG00000031558 ENSESTT00000079851 Transcript downstream_gene_variant - - - - - - DISTANCE=2443 rs10744686 12:5669792 T ENSESTG00000031558 ENSESTT00000079837 Transcript intron_variant - - - - - - rs10744686 12:5669792 T 57101 NM_020373.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2025 rs10744686 12:5669792 T ENSESTG00000031558 ENSESTT00000079807 Transcript downstream_gene_variant - - - - - - DISTANCE=2443 rs10744686 12:5669792 T ENSESTG00000031558 ENSESTT00000079800 Transcript intron_variant - - - - - - rs10744686 12:5669792 T ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs10744686 12:5669792 T ENSESTG00000031558 ENSESTT00000079843 Transcript downstream_gene_variant - - - - - - DISTANCE=2443 rs10744686 12:5669792 T ENSESTG00000031558 ENSESTT00000079750 Transcript downstream_gene_variant - - - - - - DISTANCE=2443 rs10744686 12:5669792 T CCDS44807.1 CCDS44807.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2673 rs6489640 12:5675511 C - ENSR00001461102 RegulatoryFeature regulatory_region_variant - - - - - - rs6489640 12:5675511 C ENSESTG00000031558 ENSESTT00000079851 Transcript intron_variant - - - - - - rs6489640 12:5675511 C ENSESTG00000031558 ENSESTT00000079837 Transcript intron_variant - - - - - - rs6489640 12:5675511 C 57101 NM_020373.2 Transcript intron_variant - - - - - - rs6489640 12:5675511 C ENSESTG00000031558 ENSESTT00000079807 Transcript intron_variant - - - - - - rs6489640 12:5675511 C ENSESTG00000031558 ENSESTT00000079800 Transcript intron_variant - - - - - - rs6489640 12:5675511 C ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs6489640 12:5675511 C ENSESTG00000031558 ENSESTT00000079843 Transcript intron_variant - - - - - - rs6489640 12:5675511 C ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs6489640 12:5675511 C CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079824 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079837 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079760 Transcript intron_variant - - - - - - rs393180 12:5772329 G 57101 NM_020373.2 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079765 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079807 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079814 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079800 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079843 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079774 Transcript intron_variant - - - - - - rs393180 12:5772329 G CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs393180 12:5772329 G ENSESTG00000031558 ENSESTT00000079846 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079824 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079837 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079760 Transcript intron_variant - - - - - - rs251765 12:5780286 T 57101 NM_020373.2 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079765 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079807 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079814 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079800 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079843 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079774 Transcript intron_variant - - - - - - rs251765 12:5780286 T CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs251765 12:5780286 T ENSESTG00000031558 ENSESTT00000079846 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079824 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079837 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079760 Transcript intron_variant - - - - - - rs251762 12:5781737 G 57101 NM_020373.2 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079765 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079807 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079814 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079800 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079843 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079774 Transcript intron_variant - - - - - - rs251762 12:5781737 G CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs251762 12:5781737 G ENSESTG00000031558 ENSESTT00000079846 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079824 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079837 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079760 Transcript intron_variant - - - - - - rs251761 12:5784836 T 57101 NM_020373.2 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079765 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079807 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079814 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079800 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079843 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079774 Transcript intron_variant - - - - - - rs251761 12:5784836 T CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs251761 12:5784836 T ENSESTG00000031558 ENSESTT00000079846 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079824 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079837 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079760 Transcript intron_variant - - - - - - rs251759 12:5786675 T 57101 NM_020373.2 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079765 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079807 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079814 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079800 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079843 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079774 Transcript intron_variant - - - - - - rs251759 12:5786675 T CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs251759 12:5786675 T ENSESTG00000031558 ENSESTT00000079846 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079824 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079837 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079760 Transcript intron_variant - - - - - - rs251757 12:5788204 G 57101 NM_020373.2 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079765 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079807 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079814 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079800 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079843 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079774 Transcript intron_variant - - - - - - rs251757 12:5788204 G CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs251757 12:5788204 G ENSESTG00000031558 ENSESTT00000079846 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079824 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079837 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079760 Transcript intron_variant - - - - - - rs380317 12:5800725 G 57101 NM_020373.2 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079765 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079807 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079814 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079800 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079843 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079774 Transcript intron_variant - - - - - - rs380317 12:5800725 G CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs380317 12:5800725 G ENSESTG00000031558 ENSESTT00000079846 Transcript intron_variant - - - - - - rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079824 Transcript upstream_gene_variant - - - - - - DISTANCE=2667 rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079818 Transcript upstream_gene_variant - - - - - - DISTANCE=959 rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079760 Transcript intron_variant - - - - - - rs1541531 12:5851236 G 57101 NM_020373.2 Transcript intron_variant - - - - - - rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079785 Transcript intron_variant - - - - - - rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079765 Transcript intron_variant - - - - - - rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079807 Transcript upstream_gene_variant - - - - - - DISTANCE=943 rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079814 Transcript upstream_gene_variant - - - - - - DISTANCE=943 rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079800 Transcript upstream_gene_variant - - - - - - DISTANCE=943 rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079792 Transcript intron_variant - - - - - - rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs1541531 12:5851236 G ENSESTG00000031558 ENSESTT00000079774 Transcript intron_variant - - - - - - rs1541531 12:5851236 G CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079824 Transcript upstream_gene_variant - - - - - - DISTANCE=2815 rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079818 Transcript upstream_gene_variant - - - - - - DISTANCE=1107 rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079760 Transcript intron_variant - - - - - - rs1541530 12:5851384 C 57101 NM_020373.2 Transcript intron_variant - - - - - - rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079785 Transcript intron_variant - - - - - - rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079765 Transcript intron_variant - - - - - - rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079807 Transcript upstream_gene_variant - - - - - - DISTANCE=1091 rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079814 Transcript upstream_gene_variant - - - - - - DISTANCE=1091 rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079800 Transcript upstream_gene_variant - - - - - - DISTANCE=1091 rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079792 Transcript intron_variant - - - - - - rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079730 Transcript intron_variant - - - - - - rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079750 Transcript intron_variant - - - - - - rs1541530 12:5851384 C ENSESTG00000031558 ENSESTT00000079774 Transcript intron_variant - - - - - - rs1541530 12:5851384 C CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs2080106 12:5862898 T ENSESTG00000031558 ENSESTT00000079760 Transcript upstream_gene_variant - - - - - - DISTANCE=2761 rs2080106 12:5862898 T 57101 NM_020373.2 Transcript intron_variant - - - - - - rs2080106 12:5862898 T ENSESTG00000031558 ENSESTT00000079785 Transcript upstream_gene_variant - - - - - - DISTANCE=2761 rs2080106 12:5862898 T ENSESTG00000031558 ENSESTT00000079765 Transcript upstream_gene_variant - - - - - - DISTANCE=2761 rs2080106 12:5862898 T ENSESTG00000031558 ENSESTT00000079730 Transcript upstream_gene_variant - - - - - - DISTANCE=2761 rs2080106 12:5862898 T ENSESTG00000031558 ENSESTT00000079750 Transcript upstream_gene_variant - - - - - - DISTANCE=2761 rs2080106 12:5862898 T ENSESTG00000031558 ENSESTT00000079774 Transcript upstream_gene_variant - - - - - - DISTANCE=2761 rs2080106 12:5862898 T CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs2362469 12:5864345 G ENSESTG00000031558 ENSESTT00000079760 Transcript upstream_gene_variant - - - - - - DISTANCE=4208 rs2362469 12:5864345 G 57101 NM_020373.2 Transcript intron_variant - - - - - - rs2362469 12:5864345 G ENSESTG00000031558 ENSESTT00000079785 Transcript upstream_gene_variant - - - - - - DISTANCE=4208 rs2362469 12:5864345 G ENSESTG00000031558 ENSESTT00000079765 Transcript upstream_gene_variant - - - - - - DISTANCE=4208 rs2362469 12:5864345 G ENSESTG00000031558 ENSESTT00000079730 Transcript upstream_gene_variant - - - - - - DISTANCE=4208 rs2362469 12:5864345 G ENSESTG00000031558 ENSESTT00000079750 Transcript upstream_gene_variant - - - - - - DISTANCE=4208 rs2362469 12:5864345 G ENSESTG00000031558 ENSESTT00000079774 Transcript upstream_gene_variant - - - - - - DISTANCE=4208 rs2362469 12:5864345 G CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs2078506 12:5869223 C 57101 NM_020373.2 Transcript intron_variant - - - - - - rs2078506 12:5869223 C CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs10735054 12:5874131 G 57101 NM_020373.2 Transcript intron_variant - - - - - - rs10735054 12:5874131 G CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs1468706 12:5876004 C 57101 NM_020373.2 Transcript intron_variant - - - - - - rs1468706 12:5876004 C CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs1990487 12:5879420 T 57101 NM_020373.2 Transcript intron_variant - - - - - - rs1990487 12:5879420 T CCDS44807.1 CCDS44807.1 Transcript intron_variant - - - - - - rs216869 12:6091924 G ENSESTG00000013216 ENSESTT00000033240 Transcript downstream_gene_variant - - - - - - DISTANCE=2806 rs216869 12:6091924 G ENSESTG00000013273 ENSESTT00000033312 Transcript intron_variant - - - - - - rs216869 12:6091924 G CCDS8539.1 CCDS8539.1 Transcript intron_variant - - - - - - rs216869 12:6091924 G 7450 NM_000552.3 Transcript intron_variant - - - - - - rs9668222 12:6352292 A ENSESTG00000012426 ENSESTT00000031191 Transcript downstream_gene_variant - - - - - - DISTANCE=4866 rs9668222 12:6352292 A 928 NM_001769.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4855 rs9668222 12:6352292 A ENSESTG00000012426 ENSESTT00000031175 Transcript downstream_gene_variant - - - - - - DISTANCE=4866 rs9668222 12:6352292 A ENSESTG00000012426 ENSESTT00000031181 Transcript downstream_gene_variant - - - - - - DISTANCE=4866 rs9668222 12:6352292 A ENSESTG00000012426 ENSESTT00000031192 Transcript downstream_gene_variant - - - - - - DISTANCE=4866 rs9668222 12:6352292 A ENSESTG00000012426 ENSESTT00000031195 Transcript downstream_gene_variant - - - - - - DISTANCE=4866 rs10849443 12:6439255 G CCDS8541.1 CCDS8541.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1944 rs10849443 12:6439255 G ENSESTG00000013155 ENSESTT00000033099 Transcript intron_variant - - - - - - rs10849443 12:6439255 G CCDS8542.1 CCDS8542.1 Transcript intron_variant - - - - - - rs10849443 12:6439255 G ENSESTG00000013155 ENSESTT00000033124 Transcript intron_variant - - - - - - rs10849443 12:6439255 G ENSESTG00000013155 ENSESTT00000033120 Transcript downstream_gene_variant - - - - - - DISTANCE=3368 rs10849443 12:6439255 G 55200 NM_001144856.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1583 rs10849443 12:6439255 G ENSESTG00000013155 ENSESTT00000032992 Transcript downstream_gene_variant - - - - - - DISTANCE=4792 rs10849443 12:6439255 G ENSESTG00000013155 ENSESTT00000033051 Transcript intron_variant - - - - - - rs10849443 12:6439255 G 55200 NM_018173.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1583 rs10849443 12:6439255 G 55200 NM_001144857.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1583 rs10849443 12:6439255 G ENSESTG00000013155 ENSESTT00000033122 Transcript intron_variant - - - - - - rs10849443 12:6439255 G ENSESTG00000012451 ENSESTT00000031236 Transcript downstream_gene_variant - - - - - - DISTANCE=2357 rs10849443 12:6439255 G ENSESTG00000013155 ENSESTT00000033063 Transcript intron_variant - - - - - - rs10849443 12:6439255 G CCDS44808.1 CCDS44808.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1944 rs10849443 12:6439255 G 7132 NM_001065.3 Transcript intron_variant - - - - - - rs6489714 12:6481587 T - ENSR00000425775 RegulatoryFeature regulatory_region_variant - - - - - - rs6489714 12:6481587 T ENSESTG00000012873 ENSESTT00000032318 Transcript intron_variant - - - - - - rs6489714 12:6481587 T ENSESTG00000012462 ENSESTT00000031248 Transcript intron_variant - - - - - - rs6489714 12:6481587 T CCDS53738.1 CCDS53738.1 Transcript intron_variant - - - - - - rs6489714 12:6481587 T ENSESTG00000012873 ENSESTT00000032322 Transcript intron_variant - - - - - - rs6489714 12:6481587 T 6337 NM_001038.5 Transcript intron_variant - - - - - - rs6489714 12:6481587 T CCDS8543.1 CCDS8543.1 Transcript intron_variant - - - - - - rs6489714 12:6481587 T ENSESTG00000012873 ENSESTT00000032316 Transcript intron_variant - - - - - - rs6489714 12:6481587 T ENSESTG00000012468 ENSESTT00000031305 Transcript upstream_gene_variant - - - - - - DISTANCE=2803 rs6489714 12:6481587 T 6337 NM_001159576.1 Transcript intron_variant - - - - - - rs6489714 12:6481587 T ENSESTG00000012873 ENSESTT00000032324 Transcript intron_variant - - - - - - rs6489714 12:6481587 T 6337 NM_001159575.1 Transcript intron_variant - - - - - - rs6489714 12:6481587 T CCDS53739.1 CCDS53739.1 Transcript intron_variant - - - - - - rs6489714 12:6481587 T ENSESTG00000012873 ENSESTT00000032307 Transcript intron_variant - - - - - - rs2532507 12:6552949 G - ENSR00000425790 RegulatoryFeature regulatory_region_variant - - - - - - rs2532507 12:6552949 G ENSESTG00000012493 ENSESTT00000031372 Transcript upstream_gene_variant - - - - - - DISTANCE=1175 rs2532507 12:6552949 G 678655 NR_015382.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2532507 12:6552949 G CCDS8545.1 CCDS8545.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1313 rs2532507 12:6552949 G 939 NM_001242.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1102 rs2532507 12:6552949 G ENSESTG00000013150 ENSESTT00000032957 Transcript upstream_gene_variant - - - - - - DISTANCE=141 rs6489729 12:6794294 G ENSESTG00000012950 ENSESTT00000032514 Transcript intron_variant - - - - - - rs6489729 12:6794294 G 171017 NM_133476.4 Transcript intron_variant - - - - - - rs6489729 12:6794294 G ENSESTG00000012950 ENSESTT00000032529 Transcript intron_variant - - - - - - rs6489729 12:6794294 G 171017 NM_001135734.2 Transcript intron_variant - - - - - - rs6489729 12:6794294 G ENSESTG00000012950 ENSESTT00000032537 Transcript intron_variant - - - - - - rs6489729 12:6794294 G ENSESTG00000012950 ENSESTT00000032527 Transcript intron_variant - - - - - - rs6489729 12:6794294 G ENSESTG00000012950 ENSESTT00000032526 Transcript intron_variant - - - - - - rs6489729 12:6794294 G 171017 NM_001039920.2 Transcript intron_variant - - - - - - rs6489729 12:6794294 G ENSESTG00000012950 ENSESTT00000032539 Transcript intron_variant - - - - - - rs10849498 12:6804902 G - ENSR00000653012 RegulatoryFeature regulatory_region_variant - - - - - - rs10849498 12:6804902 G ENSESTG00000012940 ENSESTT00000032458 Transcript downstream_gene_variant - - - - - - DISTANCE=753 rs10849498 12:6804902 G 196500 NM_001244015.1 Transcript intron_variant - - - - - - rs10849498 12:6804902 G ENSESTG00000012635 ENSESTT00000031753 Transcript upstream_gene_variant - - - - - - DISTANCE=2888 rs10849498 12:6804902 G CCDS58205.1 CCDS58205.1 Transcript intron_variant - - - - - - rs10849498 12:6804902 G 196500 NM_001244014.1 Transcript intron_variant - - - - - - rs10849498 12:6804902 G 196500 NM_153685.3 Transcript intron_variant - - - - - - rs10849498 12:6804902 G CCDS44818.1 CCDS44818.1 Transcript intron_variant - - - - - - rs10849498 12:6804902 G ENSESTG00000012635 ENSESTT00000031748 Transcript upstream_gene_variant - - - - - - DISTANCE=2888 rs2857231 12:6902252 A 920 NM_001195015.2 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031877 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031907 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031898 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031897 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031890 Transcript intron_variant - - - - - - rs2857231 12:6902252 A 920 NM_001195017.2 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031883 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031895 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031886 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031910 Transcript intron_variant - - - - - - rs2857231 12:6902252 A 920 NM_001195014.2 Transcript intron_variant - - - - - - rs2857231 12:6902252 A 920 NM_000616.4 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031905 Transcript intron_variant - - - - - - rs2857231 12:6902252 A 920 NM_001195016.2 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031893 Transcript intron_variant - - - - - - rs2857231 12:6902252 A ENSESTG00000012689 ENSESTT00000031887 Transcript intron_variant - - - - - - rs4963522 12:6914872 A 920 NM_001195015.2 Transcript intron_variant - - - - - - rs4963522 12:6914872 A CCDS8562.1 CCDS8562.1 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031877 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031907 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031898 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031897 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031890 Transcript intron_variant - - - - - - rs4963522 12:6914872 A 920 NM_001195017.2 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031883 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031895 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031886 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031910 Transcript intron_variant - - - - - - rs4963522 12:6914872 A 920 NM_001195014.2 Transcript intron_variant - - - - - - rs4963522 12:6914872 A 920 NM_000616.4 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031905 Transcript intron_variant - - - - - - rs4963522 12:6914872 A 920 NM_001195016.2 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031893 Transcript intron_variant - - - - - - rs4963522 12:6914872 A ENSESTG00000012689 ENSESTT00000031887 Transcript intron_variant - - - - - - rs7979180 12:6957146 A ENSESTG00000012763 ENSESTT00000032094 Transcript downstream_gene_variant - - - - - - DISTANCE=630 rs7979180 12:6957146 A ENSESTG00000012763 ENSESTT00000032067 Transcript downstream_gene_variant - - - - - - DISTANCE=2177 rs7979180 12:6957146 A ENSESTG00000012786 ENSESTT00000032176 Transcript upstream_gene_variant - - - - - - DISTANCE=4160 rs7979180 12:6957146 A 8078 NM_003481.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4145 rs7979180 12:6957146 A CCDS8564.1 CCDS8564.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1084 rs7979180 12:6957146 A ENSESTG00000012763 ENSESTT00000032077 Transcript downstream_gene_variant - - - - - - DISTANCE=773 rs7979180 12:6957146 A ENSESTG00000012763 ENSESTT00000032084 Transcript downstream_gene_variant - - - - - - DISTANCE=773 rs7979180 12:6957146 A 2784 NM_002075.2 Transcript downstream_gene_variant - - - - - - DISTANCE=589 rs7979180 12:6957146 A 83461 NM_031299.4 Transcript downstream_gene_variant - - - - - - DISTANCE=826 rs7979180 12:6957146 A ENSESTG00000012763 ENSESTT00000032063 Transcript downstream_gene_variant - - - - - - DISTANCE=773 rs7979180 12:6957146 A ENSESTG00000012763 ENSESTT00000032087 Transcript downstream_gene_variant - - - - - - DISTANCE=2177 rs7979180 12:6957146 A ENSESTG00000012763 ENSESTT00000032079 Transcript downstream_gene_variant - - - - - - DISTANCE=2177 rs7979180 12:6957146 A 8078 NM_001098536.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4139 rs7979180 12:6957146 A CCDS8565.1 CCDS8565.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1061 rs7979180 12:6957146 A CCDS31733.1 CCDS31733.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4198 rs7979180 12:6957146 A CCDS41743.1 CCDS41743.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4198 rs10744719 12:6964118 C 8078 NM_003481.2 Transcript intron_variant - - - - - - rs10744719 12:6964118 C CCDS31733.1 CCDS31733.1 Transcript intron_variant - - - - - - rs10744719 12:6964118 C 8078 NM_001098536.1 Transcript intron_variant - - - - - - rs10744719 12:6964118 C 83461 NM_031299.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3662 rs10744719 12:6964118 C CCDS41743.1 CCDS41743.1 Transcript intron_variant - - - - - - rs10744719 12:6964118 C CCDS8565.1 CCDS8565.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4002 rs10744719 12:6964118 C ENSESTG00000012786 ENSESTT00000032176 Transcript intron_variant - - - - - - rs7975262 12:7300080 T ENSESTG00000031031 ENSESTT00000078267 Transcript intron_variant - - - - - - rs7975262 12:7300080 T ENSESTG00000031031 ENSESTT00000078112 Transcript intron_variant - - - - - - rs7975262 12:7300080 T ENSESTG00000031598 ENSESTT00000079694 Transcript intron_variant - - - - - - rs7975262 12:7300080 T ENSESTG00000031031 ENSESTT00000078167 Transcript intron_variant - - - - - - rs7975262 12:7300080 T ENSESTG00000031031 ENSESTT00000078315 Transcript upstream_gene_variant - - - - - - DISTANCE=1486 rs7975262 12:7300080 T CCDS8575.1 CCDS8575.1 Transcript intron_variant - - - - - - rs7975262 12:7300080 T 9746 NM_014718.3 Transcript intron_variant - - - - - - rs7975262 12:7300080 T ENSESTG00000031031 ENSESTT00000078284 Transcript intron_variant - - - - - - rs7135683 12:7915976 A CCDS44826.1 CCDS44826.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1906 rs7135683 12:7915976 A 360030 NM_001145465.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1836 rs7973579 12:8178349 G - - - intergenic_variant - - - - - - rs3111343 12:8358315 G ENSESTG00000016011 ENSESTT00000040146 Transcript intron_variant - - - - - - rs3111343 12:8358315 G 440078 NR_026788.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4719 rs2719021 12:8464206 A - - - intergenic_variant - - - - - - rs7960144 12:8633544 C CCDS31739.1 CCDS31739.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3484 rs7960144 12:8633544 C 93978 NM_001007033.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2618 rs2401403 12:9959198 C ENSESTG00000030485 ENSESTT00000076755 Transcript intron_variant - - - - - - rs4764386 12:10450458 A ENSESTG00000029019 ENSESTT00000073066 Transcript intron_variant - - - - - - rs4764386 12:10450458 A ENSESTG00000028251 ENSESTT00000071058 Transcript intron_variant - - - - - - rs39629 12:10862023 T ENSESTG00000028581 ENSESTT00000072161 Transcript intron_variant - - - - - - rs39629 12:10862023 T ENSESTG00000028581 ENSESTT00000072178 Transcript downstream_gene_variant - - - - - - DISTANCE=928 rs39629 12:10862023 T 8531 NM_001145426.1 Transcript intron_variant - - - - - - rs39629 12:10862023 T ENSESTG00000028581 ENSESTT00000072127 Transcript downstream_gene_variant - - - - - - DISTANCE=3783 rs39629 12:10862023 T ENSESTG00000028283 ENSESTT00000071132 Transcript intron_variant - - - - - - rs39629 12:10862023 T CCDS8630.1 CCDS8630.1 Transcript intron_variant - - - - - - rs39629 12:10862023 T 8531 NM_003651.4 Transcript intron_variant - - - - - - rs39629 12:10862023 T ENSESTG00000028581 ENSESTT00000072110 Transcript intron_variant - - - - - - rs39629 12:10862023 T CCDS44831.1 CCDS44831.1 Transcript intron_variant - - - - - - rs39629 12:10862023 T ENSESTG00000028581 ENSESTT00000071997 Transcript intron_variant - - - - - - rs39629 12:10862023 T ENSESTG00000028581 ENSESTT00000072136 Transcript intron_variant - - - - - - rs2059762 12:11502784 C CCDS8642.1 CCDS8642.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3257 rs2059762 12:11502784 C CCDS55805.1 CCDS55805.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3257 rs2059762 12:11502784 C ENSESTG00000003492 ENSESTT00000008718 Transcript downstream_gene_variant - - - - - - DISTANCE=3765 rs2059762 12:11502784 C 5542 NM_199354.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1973 rs2059762 12:11502784 C 5542 NM_199353.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1973 rs2059762 12:11502784 C 5542 NM_005039.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1973 rs1212917 12:11699804 A 338817 NR_033890.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1160 rs2856317 12:11807667 T - ENSR00000653115 RegulatoryFeature regulatory_region_variant - - - - - - rs2856317 12:11807667 T 2120 NM_001987.4 Transcript intron_variant - - - - - - rs2856317 12:11807667 T ENSESTG00000003475 ENSESTT00000008692 Transcript intron_variant - - - - - - rs2856317 12:11807667 T ENSESTG00000003475 ENSESTT00000008685 Transcript intron_variant - - - - - - rs2856317 12:11807667 T CCDS8643.1 CCDS8643.1 Transcript intron_variant - - - - - - rs2710271 12:11908336 A 2120 NM_001987.4 Transcript intron_variant - - - - - - rs2710271 12:11908336 A ENSESTG00000003475 ENSESTT00000008692 Transcript downstream_gene_variant - - - - - - DISTANCE=2799 rs2710271 12:11908336 A ENSESTG00000003475 ENSESTT00000008685 Transcript intron_variant - - - - - - rs2710271 12:11908336 A CCDS8643.1 CCDS8643.1 Transcript intron_variant - - - - - - rs3983833 12:12117276 G - - - intergenic_variant - - - - - - rs7979485 12:12303637 T ENSESTG00000004117 ENSESTT00000010376 Transcript intron_variant - - - - - - rs7979485 12:12303637 T 4040 NM_002336.2 Transcript intron_variant - - - - - - rs7979485 12:12303637 T CCDS8647.1 CCDS8647.1 Transcript intron_variant - - - - - - rs7314166 12:12323964 C ENSESTG00000004247 ENSESTT00000010688 Transcript intron_variant - - - - - - rs7314166 12:12323964 C 4040 NM_002336.2 Transcript intron_variant - - - - - - rs7314166 12:12323964 C CCDS8647.1 CCDS8647.1 Transcript intron_variant - - - - - - rs7306943 12:12557671 C CCDS8649.1 CCDS8649.1 Transcript intron_variant - - - - - - rs7306943 12:12557671 C ENSESTG00000004123 ENSESTT00000010418 Transcript intron_variant - - - - - - rs7306943 12:12557671 C 118426 NM_058169.3 Transcript intron_variant - - - - - - rs7300225 12:12678142 A ENSESTG00000004209 ENSESTT00000010628 Transcript intron_variant - - - - - - rs7300225 12:12678142 A 80824 NM_030640.2 Transcript intron_variant - - - - - - rs7300225 12:12678142 A ENSESTG00000004209 ENSESTT00000010622 Transcript intron_variant - - - - - - rs7300225 12:12678142 A ENSESTG00000004209 ENSESTT00000010633 Transcript intron_variant - - - - - - rs7300225 12:12678142 A CCDS8650.1 CCDS8650.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4110 rs888545 12:12791859 G CCDS8651.1 CCDS8651.1 Transcript intron_variant - - - - - - rs888545 12:12791859 G ENSESTG00000004133 ENSESTT00000010437 Transcript downstream_gene_variant - - - - - - DISTANCE=1311 rs888545 12:12791859 G ENSESTG00000004133 ENSESTT00000010445 Transcript downstream_gene_variant - - - - - - DISTANCE=1223 rs888545 12:12791859 G ENSESTG00000004204 ENSESTT00000010585 Transcript upstream_gene_variant - - - - - - DISTANCE=2984 rs888545 12:12791859 G 1389 NM_001310.2 Transcript intron_variant - - - - - - rs2900305 12:13175091 C ENSESTG00000004635 ENSESTT00000011701 Transcript downstream_gene_variant - - - - - - DISTANCE=2203 rs2417267 12:13399519 C - - - intergenic_variant - - - - - - rs4763965 12:13471242 C - - - intergenic_variant - - - - - - rs11055410 12:13563567 A - - - intergenic_variant - - - - - - rs4763981 12:13574363 T - - - intergenic_variant - - - - - - rs7305308 12:13718602 A CCDS8662.1 CCDS8662.1 Transcript intron_variant - - - - - - rs7305308 12:13718602 A 2904 NM_000834.3 Transcript intron_variant - - - - - - rs10734872 12:14303987 A - - - intergenic_variant - - - - - - rs7962384 12:14318551 G - - - intergenic_variant - - - - - - rs10744048 12:14338848 G - ENSR00000426815 RegulatoryFeature regulatory_region_variant - - - - - - rs10744048 12:14338848 G - - - intergenic_variant - - - - - - rs7300554 12:14340438 G - - - intergenic_variant - - - - - - rs10845921 12:14361021 C - - - intergenic_variant - - - - - - rs7303645 12:14420882 A - - - intergenic_variant - - - - - - rs10734874 12:14470266 A - ENSR00000426834 RegulatoryFeature regulatory_region_variant - - - - - - rs10734874 12:14470266 A - - - intergenic_variant - - - - - - rs10744059 12:14485446 G - - - intergenic_variant - - - - - - rs7312233 12:14551610 C ENSESTG00000007475 ENSESTT00000018887 Transcript intron_variant - - - - - - rs7312233 12:14551610 C ENSESTG00000007475 ENSESTT00000018899 Transcript intron_variant - - - - - - rs7312233 12:14551610 C ENSESTG00000007475 ENSESTT00000018866 Transcript intron_variant - - - - - - rs7312233 12:14551610 C ENSESTG00000007475 ENSESTT00000018858 Transcript intron_variant - - - - - - rs7312233 12:14551610 C 55729 NM_018179.3 Transcript intron_variant - - - - - - rs7312233 12:14551610 C ENSESTG00000007475 ENSESTT00000018860 Transcript intron_variant - - - - - - rs6488686 12:14578969 G ENSESTG00000007475 ENSESTT00000018887 Transcript downstream_gene_variant - - - - - - DISTANCE=1526 rs6488686 12:14578969 G ENSESTG00000007475 ENSESTT00000018922 Transcript downstream_gene_variant - - - - - - DISTANCE=1526 rs6488686 12:14578969 G ENSESTG00000007475 ENSESTT00000018899 Transcript downstream_gene_variant - - - - - - DISTANCE=1526 rs6488686 12:14578969 G ENSESTG00000007475 ENSESTT00000018905 Transcript downstream_gene_variant - - - - - - DISTANCE=1526 rs6488686 12:14578969 G ENSESTG00000007475 ENSESTT00000018902 Transcript downstream_gene_variant - - - - - - DISTANCE=1526 rs6488686 12:14578969 G CCDS8663.1 CCDS8663.1 Transcript intron_variant - - - - - - rs6488686 12:14578969 G ENSESTG00000007475 ENSESTT00000018858 Transcript downstream_gene_variant - - - - - - DISTANCE=1526 rs6488686 12:14578969 G ENSESTG00000007475 ENSESTT00000018866 Transcript downstream_gene_variant - - - - - - DISTANCE=1526 rs6488686 12:14578969 G 55729 NM_018179.3 Transcript intron_variant - - - - - - rs6488686 12:14578969 G ENSESTG00000007475 ENSESTT00000018860 Transcript downstream_gene_variant - - - - - - DISTANCE=1526 rs10772781 12:14585084 C CCDS8663.1 CCDS8663.1 Transcript intron_variant - - - - - - rs10772781 12:14585084 C ENSESTG00000007514 ENSESTT00000018937 Transcript upstream_gene_variant - - - - - - DISTANCE=3956 rs10772781 12:14585084 C 55729 NM_018179.3 Transcript intron_variant - - - - - - rs7298671 12:14585483 C CCDS8663.1 CCDS8663.1 Transcript intron_variant - - - - - - rs7298671 12:14585483 C ENSESTG00000007514 ENSESTT00000018937 Transcript upstream_gene_variant - - - - - - DISTANCE=3557 rs7298671 12:14585483 C 55729 NM_018179.3 Transcript intron_variant - - - - - - rs10160952 12:14585904 A CCDS8663.1 CCDS8663.1 Transcript intron_variant - - - - - - rs10160952 12:14585904 A ENSESTG00000007514 ENSESTT00000018937 Transcript upstream_gene_variant - - - - - - DISTANCE=3136 rs10160952 12:14585904 A 55729 NM_018179.3 Transcript intron_variant - - - - - - rs10734877 12:14627614 T ENSESTG00000007524 ENSESTT00000019002 Transcript intron_variant - - - - - - rs10734877 12:14627614 T ENSESTG00000007524 ENSESTT00000018995 Transcript intron_variant - - - - - - rs10734877 12:14627614 T CCDS8663.1 CCDS8663.1 Transcript intron_variant - - - - - - rs10734877 12:14627614 T 55729 NM_018179.3 Transcript intron_variant - - - - - - rs10734877 12:14627614 T ENSESTG00000007524 ENSESTT00000018997 Transcript intron_variant - - - - - - rs2098546 12:14637654 G ENSESTG00000007524 ENSESTT00000018995 Transcript intron_variant - - - - - - rs2098546 12:14637654 G CCDS8663.1 CCDS8663.1 Transcript intron_variant - - - - - - rs2098546 12:14637654 G 55729 NM_018179.3 Transcript intron_variant - - - - - - rs2098546 12:14637654 G ENSESTG00000007524 ENSESTT00000018997 Transcript downstream_gene_variant - - - - - - DISTANCE=2814 rs4462398 12:14675947 T 79887 NM_024829.5 Transcript intron_variant - - - - - - rs4462398 12:14675947 T CCDS31751.1 CCDS31751.1 Transcript intron_variant - - - - - - rs4462398 12:14675947 T ENSESTG00000007645 ENSESTT00000019294 Transcript intron_variant - - - - - - rs247330 12:14847551 T CCDS8664.1 CCDS8664.1 Transcript intron_variant - - - - - - rs247330 12:14847551 T ENSESTG00000007622 ENSESTT00000019204 Transcript intron_variant - - - - - - rs247330 12:14847551 T 2984 NM_004963.3 Transcript intron_variant - - - - - - rs247343 12:14851452 G CCDS8664.1 CCDS8664.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2070 rs247343 12:14851452 G ENSESTG00000007622 ENSESTT00000019204 Transcript upstream_gene_variant - - - - - - DISTANCE=1933 rs247343 12:14851452 G 2984 NM_004963.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1933 rs10744077 12:14865246 A - - - intergenic_variant - - - - - - rs6488710 12:14929872 G - ENSR00000426888 RegulatoryFeature regulatory_region_variant - - - - - - rs6488710 12:14929872 G 55766 NR_027716.1 Transcript non_coding_exon_variant,nc_transcript_variant 2289 - - - - - rs6488710 12:14929872 G CCDS31752.1 CCDS31752.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2078 rs6488710 12:14929872 G 55766 NM_177925.2 Transcript 3_prime_UTR_variant 2603 - - - - - rs10082988 12:14937001 G CCDS8666.1 CCDS8666.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2998 rs10082988 12:14937001 G ENSESTG00000007562 ENSESTT00000019036 Transcript upstream_gene_variant - - - - - - DISTANCE=4976 rs10082988 12:14937001 G 51729 NM_016312.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2411 rs2445403 12:15030049 C 4256 NM_000900.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4066 rs2445403 12:15030049 C 4256 NM_001190839.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4066 rs2445403 12:15030049 C ENSESTG00000007570 ENSESTT00000019066 Transcript intron_variant - - - - - - rs2430694 12:15072410 G 121506 NM_152321.2 Transcript intron_variant - - - - - - rs2430694 12:15072410 G ENSESTG00000018370 ENSESTT00000046304 Transcript intron_variant - - - - - - rs2430694 12:15072410 G CCDS8670.1 CCDS8670.1 Transcript intron_variant - - - - - - rs2430694 12:15072410 G ENSESTG00000018370 ENSESTT00000046295 Transcript intron_variant - - - - - - rs2080544 12:15091978 C 121506 NM_152321.2 Transcript upstream_gene_variant - - - - - - DISTANCE=515 rs2080544 12:15091978 C ENSESTG00000018293 ENSESTT00000046153 Transcript downstream_gene_variant - - - - - - DISTANCE=3530 rs2080544 12:15091978 C ENSESTG00000018293 ENSESTT00000046212 Transcript downstream_gene_variant - - - - - - DISTANCE=3386 rs2080544 12:15091978 C CCDS8670.1 CCDS8670.1 Transcript upstream_gene_variant - - - - - - DISTANCE=536 rs2080544 12:15091978 C CCDS8671.1 CCDS8671.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3478 rs2080544 12:15091978 C 397 NM_001175.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2972 rs2080544 12:15091978 C ENSESTG00000018370 ENSESTT00000046295 Transcript upstream_gene_variant - - - - - - DISTANCE=523 rs2430711 12:15103605 G - ENSR00001461620 RegulatoryFeature regulatory_region_variant - - - - - - rs2430711 12:15103605 G ENSESTG00000018293 ENSESTT00000046153 Transcript synonymous_variant 281 42 14 D gaT/gaC - rs2430711 12:15103605 G ENSESTG00000018293 ENSESTT00000046212 Transcript synonymous_variant 110 42 14 D gaT/gaC - rs2430711 12:15103605 G CCDS8671.1 CCDS8671.1 Transcript synonymous_variant 42 42 14 D gaT/gaC - rs2430711 12:15103605 G 397 NM_001175.4 Transcript synonymous_variant 146 42 14 D gaT/gaC - rs7970745 12:15216178 T - - - intergenic_variant - - - - - - rs1074999 12:15255285 T - - - intergenic_variant - - - - - - rs6488756 12:15307386 T 85004 NM_001190726.1 Transcript intron_variant - - - - - - rs6488756 12:15307386 T ENSESTG00000017875 ENSESTT00000045018 Transcript intron_variant - - - - - - rs6488756 12:15307386 T ENSESTG00000018241 ENSESTT00000046044 Transcript intron_variant - - - - - - rs6488756 12:15307386 T 85004 NM_032918.2 Transcript intron_variant - - - - - - rs6488756 12:15307386 T CCDS53753.1 CCDS53753.1 Transcript intron_variant - - - - - - rs6488756 12:15307386 T CCDS8673.1 CCDS8673.1 Transcript intron_variant - - - - - - rs4764175 12:15312210 C 85004 NM_001190726.1 Transcript intron_variant - - - - - - rs4764175 12:15312210 C ENSESTG00000017875 ENSESTT00000045018 Transcript downstream_gene_variant - - - - - - DISTANCE=3997 rs4764175 12:15312210 C ENSESTG00000018241 ENSESTT00000046044 Transcript intron_variant - - - - - - rs4764175 12:15312210 C 85004 NM_032918.2 Transcript intron_variant - - - - - - rs4764175 12:15312210 C CCDS53753.1 CCDS53753.1 Transcript intron_variant - - - - - - rs4764175 12:15312210 C CCDS8673.1 CCDS8673.1 Transcript intron_variant - - - - - - rs1073383 12:15328537 T 85004 NM_001190726.1 Transcript intron_variant - - - - - - rs1073383 12:15328537 T ENSESTG00000018241 ENSESTT00000046044 Transcript intron_variant - - - - - - rs1073383 12:15328537 T 85004 NM_032918.2 Transcript intron_variant - - - - - - rs1073383 12:15328537 T CCDS53753.1 CCDS53753.1 Transcript intron_variant - - - - - - rs1073383 12:15328537 T CCDS8673.1 CCDS8673.1 Transcript intron_variant - - - - - - rs1034503 12:15557532 T - ENSR00001461652 RegulatoryFeature regulatory_region_variant - - - - - - rs1034503 12:15557532 T ENSESTG00000017884 ENSESTT00000045036 Transcript intron_variant - - - - - - rs1034503 12:15557532 T 5800 NM_030667.2 Transcript intron_variant - - - - - - rs1034503 12:15557532 T CCDS8675.1 CCDS8675.1 Transcript intron_variant - - - - - - rs1034503 12:15557532 T CCDS8674.1 CCDS8674.1 Transcript intron_variant - - - - - - rs1034503 12:15557532 T 5800 NM_002848.3 Transcript intron_variant - - - - - - rs253830 12:15626326 T 5800 NM_030667.2 Transcript intron_variant - - - - - - rs253830 12:15626326 T CCDS8675.1 CCDS8675.1 Transcript intron_variant - - - - - - rs253830 12:15626326 T CCDS8674.1 CCDS8674.1 Transcript intron_variant - - - - - - rs253830 12:15626326 T 5800 NM_002848.3 Transcript intron_variant - - - - - - rs253855 12:15640725 C ENSESTG00000017895 ENSESTT00000045165 Transcript intron_variant - - - - - - rs253855 12:15640725 C ENSESTG00000017895 ENSESTT00000045152 Transcript intron_variant - - - - - - rs253855 12:15640725 C 5800 NM_030667.2 Transcript intron_variant - - - - - - rs253855 12:15640725 C CCDS8675.1 CCDS8675.1 Transcript intron_variant - - - - - - rs253855 12:15640725 C CCDS8674.1 CCDS8674.1 Transcript intron_variant - - - - - - rs253855 12:15640725 C 5800 NM_002848.3 Transcript intron_variant - - - - - - rs2080471 12:15648841 C ENSESTG00000017895 ENSESTT00000045165 Transcript intron_variant - - - - - - rs2080471 12:15648841 C ENSESTG00000017895 ENSESTT00000045152 Transcript intron_variant - - - - - - rs2080471 12:15648841 C 5800 NM_030667.2 Transcript intron_variant - - - - - - rs2080471 12:15648841 C CCDS8675.1 CCDS8675.1 Transcript intron_variant - - - - - - rs2080471 12:15648841 C CCDS8674.1 CCDS8674.1 Transcript intron_variant - - - - - - rs2080471 12:15648841 C 5800 NM_002848.3 Transcript intron_variant - - - - - - rs10772858 12:15655337 A ENSESTG00000017895 ENSESTT00000045180 Transcript upstream_gene_variant - - - - - - DISTANCE=911 rs10772858 12:15655337 A ENSESTG00000017895 ENSESTT00000045165 Transcript intron_variant - - - - - - rs10772858 12:15655337 A ENSESTG00000017895 ENSESTT00000045152 Transcript intron_variant - - - - - - rs10772858 12:15655337 A 5800 NM_030667.2 Transcript intron_variant - - - - - - rs10772858 12:15655337 A CCDS8675.1 CCDS8675.1 Transcript intron_variant - - - - - - rs10772858 12:15655337 A CCDS8674.1 CCDS8674.1 Transcript intron_variant - - - - - - rs10772858 12:15655337 A 5800 NM_002848.3 Transcript intron_variant - - - - - - rs7309160 12:15780089 G ENSESTG00000018071 ENSESTT00000045880 Transcript intron_variant - - - - - - rs7309160 12:15780089 G CCDS31753.1 CCDS31753.1 Transcript intron_variant - - - - - - rs7309160 12:15780089 G 2059 NM_004447.5 Transcript intron_variant - - - - - - rs7309160 12:15780089 G ENSESTG00000018071 ENSESTT00000045813 Transcript intron_variant - - - - - - rs7309160 12:15780089 G ENSESTG00000018071 ENSESTT00000045914 Transcript intron_variant - - - - - - rs4328258 12:15781240 C - ENSR00000426986 RegulatoryFeature regulatory_region_variant - - - - - - rs4328258 12:15781240 C ENSESTG00000018071 ENSESTT00000045880 Transcript intron_variant - - - - - - rs4328258 12:15781240 C CCDS31753.1 CCDS31753.1 Transcript intron_variant - - - - - - rs4328258 12:15781240 C 2059 NM_004447.5 Transcript intron_variant - - - - - - rs4328258 12:15781240 C ENSESTG00000018071 ENSESTT00000045813 Transcript intron_variant - - - - - - rs4328258 12:15781240 C ENSESTG00000018071 ENSESTT00000045914 Transcript intron_variant - - - - - - rs10772867 12:15799812 A - ENSR00001025420 RegulatoryFeature regulatory_region_variant - - - - - - rs10772867 12:15799812 A ENSESTG00000018071 ENSESTT00000045880 Transcript intron_variant - - - - - - rs10772867 12:15799812 A CCDS31753.1 CCDS31753.1 Transcript intron_variant - - - - - - rs10772867 12:15799812 A 2059 NM_004447.5 Transcript intron_variant - - - - - - rs10772867 12:15799812 A ENSESTG00000018071 ENSESTT00000045813 Transcript intron_variant - - - - - - rs10772867 12:15799812 A ENSESTG00000018071 ENSESTT00000045914 Transcript intron_variant - - - - - - rs10772869 12:15841702 G ENSESTG00000018071 ENSESTT00000045857 Transcript intron_variant - - - - - - rs10772869 12:15841702 G ENSESTG00000018071 ENSESTT00000045849 Transcript intron_variant - - - - - - rs10772869 12:15841702 G ENSESTG00000018071 ENSESTT00000045880 Transcript intron_variant - - - - - - rs10772869 12:15841702 G 2059 NM_004447.5 Transcript intron_variant - - - - - - rs10772869 12:15841702 G ENSESTG00000018071 ENSESTT00000045813 Transcript intron_variant - - - - - - rs10772869 12:15841702 G ENSESTG00000018071 ENSESTT00000045914 Transcript intron_variant - - - - - - rs2950439 12:15852391 A ENSESTG00000018071 ENSESTT00000045857 Transcript intron_variant - - - - - - rs2950439 12:15852391 A ENSESTG00000018071 ENSESTT00000045849 Transcript intron_variant - - - - - - rs2950439 12:15852391 A ENSESTG00000018071 ENSESTT00000045880 Transcript intron_variant - - - - - - rs2950439 12:15852391 A 2059 NM_004447.5 Transcript intron_variant - - - - - - rs2950439 12:15852391 A ENSESTG00000018071 ENSESTT00000045813 Transcript intron_variant - - - - - - rs2950439 12:15852391 A ENSESTG00000018071 ENSESTT00000045914 Transcript intron_variant - - - - - - rs2417504 12:15963992 A ENSESTG00000018071 ENSESTT00000045813 Transcript intron_variant - - - - - - rs1624215 12:16309420 A - - - intergenic_variant - - - - - - rs1671474 12:16404639 A 729025 NM_001170798.1 Transcript intron_variant - - - - - - rs10846352 12:16541192 C - - - intergenic_variant - - - - - - rs2193138 12:16586027 A - - - intergenic_variant - - - - - - rs34404 12:16605585 G - - - intergenic_variant - - - - - - rs1966437 12:16710741 G 55885 NR_045013.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1966437 12:16710741 G 55885 NM_001243609.1 Transcript intron_variant - - - - - - rs1966437 12:16710741 G CCDS58210.1 CCDS58210.1 Transcript intron_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063962 Transcript downstream_gene_variant - - - - - - DISTANCE=2656 rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063941 Transcript intron_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000064008 Transcript intron_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063947 Transcript intron_variant - - - - - - rs1966437 12:16710741 G CCDS8678.1 CCDS8678.1 Transcript intron_variant - - - - - - rs1966437 12:16710741 G CCDS58212.1 CCDS58212.1 Transcript intron_variant - - - - - - rs1966437 12:16710741 G CCDS58211.1 CCDS58211.1 Transcript intron_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063993 Transcript downstream_gene_variant - - - - - - DISTANCE=2628 rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063932 Transcript intron_variant - - - - - - rs1966437 12:16710741 G 55885 NM_001243613.1 Transcript intron_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063851 Transcript downstream_gene_variant - - - - - - DISTANCE=2697 rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063907 Transcript downstream_gene_variant - - - - - - DISTANCE=2606 rs1966437 12:16710741 G 55885 NM_001243612.1 Transcript intron_variant - - - - - - rs1966437 12:16710741 G 55885 NM_001243611.1 Transcript intron_variant - - - - - - rs1966437 12:16710741 G 55885 NM_001001395.2 Transcript intron_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000064119 Transcript intron_variant - - - - - - rs1966437 12:16710741 G 55885 NM_001243610.1 Transcript intron_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063903 Transcript downstream_gene_variant - - - - - - DISTANCE=2642 rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063988 Transcript downstream_gene_variant - - - - - - DISTANCE=2611 rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000064063 Transcript downstream_gene_variant - - - - - - DISTANCE=2609 rs1966437 12:16710741 G 55885 NR_045014.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000063879 Transcript intron_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000064137 Transcript intron_variant - - - - - - rs1966437 12:16710741 G ENSESTG00000025307 ENSESTT00000064022 Transcript downstream_gene_variant - - - - - - DISTANCE=2679 rs1966437 12:16710741 G 55885 NR_045012.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1966437 12:16710741 G 55885 NM_018640.4 Transcript intron_variant - - - - - - rs10772955 12:16847050 T - - - intergenic_variant - - - - - - rs10772968 12:16962449 A - - - intergenic_variant - - - - - - rs1174640 12:17037057 C - ENSR00000653175 RegulatoryFeature regulatory_region_variant - - - - - - rs1174640 12:17037057 C - - - intergenic_variant - - - - - - rs2930792 12:17095941 T - - - intergenic_variant - - - - - - rs842465 12:17106549 C - - - intergenic_variant - - - - - - rs842477 12:17123967 T - - - intergenic_variant - - - - - - rs842469 12:17162395 C - - - intergenic_variant - - - - - - rs10744143 12:17192148 G - - - intergenic_variant - - - - - - rs3112077 12:17205393 G - - - intergenic_variant - - - - - - rs3098771 12:17205891 A - - - intergenic_variant - - - - - - rs2919888 12:17208307 T - - - intergenic_variant - - - - - - rs2919889 12:17209342 A - - - intergenic_variant - - - - - - rs3112076 12:17220475 A - - - intergenic_variant - - - - - - rs4516024 12:17228325 T - - - intergenic_variant - - - - - - rs1177403 12:17611500 G - - - intergenic_variant - - - - - - rs4505113 12:18311049 A - - - intergenic_variant - - - - - - rs10770357 12:18499777 G ENSESTG00000023689 ENSESTT00000059852 Transcript splice_region_variant,intron_variant - - - - - - rs10770357 12:18499777 G CCDS44839.1 CCDS44839.1 Transcript splice_region_variant,intron_variant - - - - - - rs10770357 12:18499777 G 5288 NM_004570.4 Transcript splice_region_variant,intron_variant - - - - - - rs10743274 12:18770174 A CCDS44839.1 CCDS44839.1 Transcript intron_variant - - - - - - rs10743274 12:18770174 A 5288 NM_004570.4 Transcript intron_variant - - - - - - rs7314247 12:19162097 G - - - intergenic_variant - - - - - - rs1514840 12:19205376 A - - - intergenic_variant - - - - - - rs7131847 12:19865372 A - ENSR00000427294 RegulatoryFeature regulatory_region_variant - - - - - - rs7131847 12:19865372 A - - - intergenic_variant - - - - - - rs2694999 12:19925617 A - - - intergenic_variant - - - - - - rs2728640 12:20114764 T - - - intergenic_variant - - - - - - rs2728582 12:20177222 C - ENSR00000427376 RegulatoryFeature regulatory_region_variant - - - - - - rs2728582 12:20177222 C 100506393 NR_040098.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2579238 12:20217799 C 100506393 NR_040098.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1554150 12:20898081 C 53919 NM_001145946.1 Transcript intron_variant - - - - - - rs1554150 12:20898081 C ENSESTG00000020232 ENSESTT00000050760 Transcript intron_variant - - - - - - rs1554150 12:20898081 C CCDS8683.1 CCDS8683.1 Transcript intron_variant - - - - - - rs1554150 12:20898081 C 53919 NM_017435.4 Transcript intron_variant - - - - - - rs1554150 12:20898081 C 53919 NM_001145945.1 Transcript intron_variant - - - - - - rs1554150 12:20898081 C CCDS53757.1 CCDS53757.1 Transcript intron_variant - - - - - - rs1554150 12:20898081 C ENSESTG00000020232 ENSESTT00000050754 Transcript intron_variant - - - - - - rs1554150 12:20898081 C 53919 NM_001145944.1 Transcript intron_variant - - - - - - rs1554150 12:20898081 C CCDS53758.1 CCDS53758.1 Transcript intron_variant - - - - - - rs1554150 12:20898081 C ENSESTG00000020232 ENSESTT00000050727 Transcript downstream_gene_variant - - - - - - DISTANCE=4775 rs1554150 12:20898081 C CCDS53759.1 CCDS53759.1 Transcript intron_variant - - - - - - rs7312878 12:21147577 C - - - intergenic_variant - - - - - - rs6487212 12:21320265 G ENSESTG00000033925 ENSESTT00000085730 Transcript intron_variant - - - - - - rs6487212 12:21320265 G 10599 NM_006446.4 Transcript intron_variant - - - - - - rs6487212 12:21320265 G ENSESTG00000033925 ENSESTT00000085764 Transcript intron_variant - - - - - - rs6487212 12:21320265 G CCDS8685.1 CCDS8685.1 Transcript intron_variant - - - - - - rs2219790 12:21418125 A CCDS8686.1 CCDS8686.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4357 rs2219790 12:21418125 A 6579 NM_134431.3 Transcript 3_prime_UTR_variant 7091 - - - - - rs2219790 12:21418125 A 6579 NM_021094.3 Transcript 3_prime_UTR_variant 6621 - - - - - rs2219790 12:21418125 A ENSESTG00000034133 ENSESTT00000086259 Transcript downstream_gene_variant - - - - - - DISTANCE=4256 rs1626023 12:21794865 T 3945 NM_002300.6 Transcript intron_variant - - - - - - rs1626023 12:21794865 T 3945 NM_001174097.1 Transcript intron_variant - - - - - - rs1626023 12:21794865 T ENSESTG00000034035 ENSESTT00000086121 Transcript intron_variant - - - - - - rs1626023 12:21794865 T CCDS8691.1 CCDS8691.1 Transcript intron_variant - - - - - - rs1650309 12:21804587 G 3945 NM_002300.6 Transcript intron_variant - - - - - - rs1650309 12:21804587 G 3945 NM_001174097.1 Transcript intron_variant - - - - - - rs1650309 12:21804587 G ENSESTG00000034035 ENSESTT00000086121 Transcript intron_variant - - - - - - rs1650309 12:21804587 G CCDS8691.1 CCDS8691.1 Transcript intron_variant - - - - - - rs2252712 12:21988386 A ENSESTG00000034019 ENSESTT00000085989 Transcript intron_variant - - - - - - rs2252712 12:21988386 A CCDS8693.1 CCDS8693.1 Transcript intron_variant - - - - - - rs2252712 12:21988386 A 10060 NM_020297.2 Transcript intron_variant - - - - - - rs2252712 12:21988386 A 10060 NM_005691.2 Transcript intron_variant - - - - - - rs2252712 12:21988386 A CCDS8694.1 CCDS8694.1 Transcript intron_variant - - - - - - rs2252707 12:21988470 A ENSESTG00000034019 ENSESTT00000085989 Transcript intron_variant - - - - - - rs2252707 12:21988470 A CCDS8693.1 CCDS8693.1 Transcript intron_variant - - - - - - rs2252707 12:21988470 A 10060 NM_020297.2 Transcript intron_variant - - - - - - rs2252707 12:21988470 A 10060 NM_005691.2 Transcript intron_variant - - - - - - rs2252707 12:21988470 A CCDS8694.1 CCDS8694.1 Transcript intron_variant - - - - - - rs2418013 12:21988533 T ENSESTG00000034019 ENSESTT00000085989 Transcript intron_variant - - - - - - rs2418013 12:21988533 T CCDS8693.1 CCDS8693.1 Transcript intron_variant - - - - - - rs2418013 12:21988533 T 10060 NM_020297.2 Transcript intron_variant - - - - - - rs2418013 12:21988533 T 10060 NM_005691.2 Transcript intron_variant - - - - - - rs2418013 12:21988533 T CCDS8694.1 CCDS8694.1 Transcript intron_variant - - - - - - rs2252702 12:21988580 T ENSESTG00000034019 ENSESTT00000085989 Transcript intron_variant - - - - - - rs2252702 12:21988580 T CCDS8693.1 CCDS8693.1 Transcript intron_variant - - - - - - rs2252702 12:21988580 T 10060 NM_020297.2 Transcript intron_variant - - - - - - rs2252702 12:21988580 T 10060 NM_005691.2 Transcript intron_variant - - - - - - rs2252702 12:21988580 T CCDS8694.1 CCDS8694.1 Transcript intron_variant - - - - - - rs704195 12:22016747 A ENSESTG00000028137 ENSESTT00000070764 Transcript intron_variant - - - - - - rs704195 12:22016747 A CCDS8693.1 CCDS8693.1 Transcript intron_variant - - - - - - rs704195 12:22016747 A 10060 NM_020297.2 Transcript intron_variant - - - - - - rs704195 12:22016747 A 10060 NM_005691.2 Transcript intron_variant - - - - - - rs704195 12:22016747 A CCDS8694.1 CCDS8694.1 Transcript intron_variant - - - - - - rs697250 12:22017422 G ENSESTG00000028137 ENSESTT00000070764 Transcript intron_variant - - - - - - rs697250 12:22017422 G CCDS8693.1 CCDS8693.1 Transcript intron_variant - - - - - - rs697250 12:22017422 G 10060 NM_020297.2 Transcript intron_variant - - - - - - rs697250 12:22017422 G 10060 NM_005691.2 Transcript intron_variant - - - - - - rs697250 12:22017422 G CCDS8694.1 CCDS8694.1 Transcript intron_variant - - - - - - rs697251 12:22017486 G ENSESTG00000028137 ENSESTT00000070764 Transcript intron_variant - - - - - - rs697251 12:22017486 G CCDS8693.1 CCDS8693.1 Transcript intron_variant - - - - - - rs697251 12:22017486 G 10060 NM_020297.2 Transcript intron_variant - - - - - - rs697251 12:22017486 G 10060 NM_005691.2 Transcript intron_variant - - - - - - rs697251 12:22017486 G CCDS8694.1 CCDS8694.1 Transcript intron_variant - - - - - - rs1517275 12:22122942 C - - - intergenic_variant - - - - - - rs7313811 12:22271036 T - - - intergenic_variant - - - - - - rs7138159 12:22683537 G ENSESTG00000027917 ENSESTT00000070314 Transcript intron_variant - - - - - - rs7138159 12:22683537 G CCDS31758.1 CCDS31758.1 Transcript intron_variant - - - - - - rs7138159 12:22683537 G 9847 NM_014802.1 Transcript intron_variant - - - - - - rs7138159 12:22683537 G ENSESTG00000027917 ENSESTT00000070345 Transcript intron_variant - - - - - - rs2453880 12:23052663 G - ENSR00000243063 RegulatoryFeature regulatory_region_variant - - - - - - rs2453880 12:23052663 G - - - intergenic_variant - - - - - - rs2453877 12:23082318 G - - - intergenic_variant - - - - - - rs4963724 12:24025905 A CCDS44844.1 CCDS44844.1 Transcript intron_variant - - - - - - rs4963724 12:24025905 A 6660 NM_001261415.1 Transcript intron_variant - - - - - - rs4963724 12:24025905 A CCDS58216.1 CCDS58216.1 Transcript intron_variant - - - - - - rs4963724 12:24025905 A ENSESTG00000002153 ENSESTT00000005343 Transcript intron_variant - - - - - - rs4963724 12:24025905 A ENSESTG00000002153 ENSESTT00000005416 Transcript intron_variant - - - - - - rs4963724 12:24025905 A ENSESTG00000029428 ENSESTT00000074083 Transcript intron_variant - - - - - - rs4963724 12:24025905 A ENSESTG00000029428 ENSESTT00000074059 Transcript intron_variant - - - - - - rs4963724 12:24025905 A ENSESTG00000002153 ENSESTT00000005389 Transcript intron_variant - - - - - - rs4963724 12:24025905 A 6660 NM_001261414.1 Transcript intron_variant - - - - - - rs4963724 12:24025905 A 6660 NM_152989.3 Transcript intron_variant - - - - - - rs4963724 12:24025905 A ENSESTG00000002153 ENSESTT00000005421 Transcript intron_variant - - - - - - rs4963724 12:24025905 A 6660 NM_006940.4 Transcript intron_variant - - - - - - rs4963724 12:24025905 A ENSESTG00000029428 ENSESTT00000074098 Transcript intron_variant - - - - - - rs4963724 12:24025905 A CCDS58217.1 CCDS58217.1 Transcript intron_variant - - - - - - rs4963724 12:24025905 A ENSESTG00000002153 ENSESTT00000005364 Transcript intron_variant - - - - - - rs4963724 12:24025905 A CCDS8699.1 CCDS8699.1 Transcript intron_variant - - - - - - rs4963724 12:24025905 A ENSESTG00000002153 ENSESTT00000005346 Transcript intron_variant - - - - - - rs1522233 12:24372766 G 6660 NM_152989.3 Transcript intron_variant - - - - - - rs1522233 12:24372766 G 6660 NM_001261414.1 Transcript intron_variant - - - - - - rs1522233 12:24372766 G ENSESTG00000029380 ENSESTT00000073968 Transcript upstream_gene_variant - - - - - - DISTANCE=3455 rs1522233 12:24372766 G ENSESTG00000029380 ENSESTT00000073955 Transcript upstream_gene_variant - - - - - - DISTANCE=3439 rs2418178 12:24589153 C 6660 NM_152989.3 Transcript intron_variant - - - - - - rs2418178 12:24589153 C 6660 NM_001261414.1 Transcript intron_variant - - - - - - rs2136018 12:24612899 G 6660 NM_152989.3 Transcript intron_variant - - - - - - rs2136018 12:24612899 G 6660 NM_001261414.1 Transcript intron_variant - - - - - - rs10161258 12:24653879 G - ENSR00000427729 RegulatoryFeature regulatory_region_variant - - - - - - rs10161258 12:24653879 G 6660 NM_152989.3 Transcript intron_variant - - - - - - rs10161258 12:24653879 G 6660 NM_001261414.1 Transcript intron_variant - - - - - - rs2970415 12:24692359 G 6660 NM_152989.3 Transcript intron_variant - - - - - - rs2970415 12:24692359 G 6660 NM_001261414.1 Transcript intron_variant - - - - - - rs4963771 12:24754239 C - ENSR00000427743 RegulatoryFeature regulatory_region_variant - - - - - - rs4963771 12:24754239 C - - - intergenic_variant - - - - - - rs1872646 12:24967291 C - ENSR00000427767 RegulatoryFeature regulatory_region_variant - - - - - - rs1872646 12:24967291 C CCDS53763.1 CCDS53763.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3651 rs1872646 12:24967291 C 586 NM_001178094.1 Transcript 3_prime_UTR_variant 5232 - - - - - rs1872646 12:24967291 C 586 NM_001178092.1 Transcript 3_prime_UTR_variant 5156 - - - - - rs1872646 12:24967291 C 586 NM_005504.6 Transcript 3_prime_UTR_variant 5339 - - - - - rs1872646 12:24967291 C CCDS53760.1 CCDS53760.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3651 rs1872646 12:24967291 C 586 NM_001178093.1 Transcript 3_prime_UTR_variant 4935 - - - - - rs1872646 12:24967291 C 586 NM_001178091.1 Transcript 3_prime_UTR_variant 5228 - - - - - rs1872646 12:24967291 C ENSESTG00000029397 ENSESTT00000073989 Transcript downstream_gene_variant - - - - - - DISTANCE=3542 rs1872646 12:24967291 C CCDS53761.1 CCDS53761.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3651 rs1872646 12:24967291 C CCDS44845.1 CCDS44845.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3651 rs1872646 12:24967291 C CCDS53762.1 CCDS53762.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3651 rs1872646 12:24967291 C ENSESTG00000029397 ENSESTT00000074035 Transcript downstream_gene_variant - - - - - - DISTANCE=3498 rs2645908 12:25090781 G - ENSR00000243152 RegulatoryFeature regulatory_region_variant - - - - - - rs2645908 12:25090781 G CCDS53763.1 CCDS53763.1 Transcript intron_variant - - - - - - rs2645908 12:25090781 G ENSESTG00000008898 ENSESTT00000022368 Transcript intron_variant - - - - - - rs2645908 12:25090781 G 586 NM_001178092.1 Transcript intron_variant - - - - - - rs2645908 12:25090781 G ENSESTG00000008898 ENSESTT00000022356 Transcript intron_variant - - - - - - rs2645908 12:25090781 G 586 NM_005504.6 Transcript intron_variant - - - - - - rs2645908 12:25090781 G 586 NM_001178091.1 Transcript intron_variant - - - - - - rs2645908 12:25090781 G CCDS44845.1 CCDS44845.1 Transcript intron_variant - - - - - - rs2645908 12:25090781 G ENSESTG00000008898 ENSESTT00000022362 Transcript intron_variant - - - - - - rs2645908 12:25090781 G CCDS53762.1 CCDS53762.1 Transcript intron_variant - - - - - - rs699044 12:25181879 G ENSESTG00000008721 ENSESTT00000021894 Transcript upstream_gene_variant - - - - - - DISTANCE=4814 rs699044 12:25181879 G 645177 XM_928212.5 Transcript intron_variant - - - - - - rs2883028 12:25285557 G ENSESTG00000008873 ENSESTT00000022277 Transcript intron_variant - - - - - - rs2883028 12:25285557 G 55259 NM_018272.3 Transcript intron_variant - - - - - - rs2883028 12:25285557 G ENSESTG00000008873 ENSESTT00000022296 Transcript intron_variant - - - - - - rs2883028 12:25285557 G 55259 NM_001204102.1 Transcript intron_variant - - - - - - rs2883028 12:25285557 G CCDS55810.1 CCDS55810.1 Transcript intron_variant - - - - - - rs2883028 12:25285557 G CCDS41762.1 CCDS41762.1 Transcript intron_variant - - - - - - rs2883028 12:25285557 G ENSESTG00000008873 ENSESTT00000022294 Transcript intron_variant - - - - - - rs2883028 12:25285557 G CCDS41763.1 CCDS41763.1 Transcript intron_variant - - - - - - rs2883028 12:25285557 G CCDS55811.1 CCDS55811.1 Transcript intron_variant - - - - - - rs2883028 12:25285557 G 55259 NM_001082973.1 Transcript intron_variant - - - - - - rs2883028 12:25285557 G 55259 NM_001204101.1 Transcript intron_variant - - - - - - rs2883028 12:25285557 G 55259 NM_001082972.1 Transcript intron_variant - - - - - - rs2883028 12:25285557 G CCDS31759.2 CCDS31759.2 Transcript intron_variant - - - - - - rs4246227 12:25304375 C - ENSR00000427825 RegulatoryFeature regulatory_region_variant - - - - - - rs4246227 12:25304375 C ENSESTG00000008873 ENSESTT00000022277 Transcript intron_variant - - - - - - rs4246227 12:25304375 C 55259 NM_018272.3 Transcript intron_variant - - - - - - rs4246227 12:25304375 C ENSESTG00000008873 ENSESTT00000022296 Transcript intron_variant - - - - - - rs4246227 12:25304375 C 55259 NM_001204102.1 Transcript intron_variant - - - - - - rs4246227 12:25304375 C CCDS55810.1 CCDS55810.1 Transcript intron_variant - - - - - - rs4246227 12:25304375 C CCDS41762.1 CCDS41762.1 Transcript intron_variant - - - - - - rs4246227 12:25304375 C ENSESTG00000008873 ENSESTT00000022294 Transcript intron_variant - - - - - - rs4246227 12:25304375 C CCDS41763.1 CCDS41763.1 Transcript intron_variant - - - - - - rs4246227 12:25304375 C CCDS55811.1 CCDS55811.1 Transcript intron_variant - - - - - - rs4246227 12:25304375 C 55259 NM_001082973.1 Transcript intron_variant - - - - - - rs4246227 12:25304375 C 55259 NM_001204101.1 Transcript intron_variant - - - - - - rs4246227 12:25304375 C ENSESTG00000008873 ENSESTT00000022306 Transcript downstream_gene_variant - - - - - - DISTANCE=2901 rs4246227 12:25304375 C ENSESTG00000008873 ENSESTT00000022300 Transcript downstream_gene_variant - - - - - - DISTANCE=2956 rs4246227 12:25304375 C 55259 NM_001082972.1 Transcript intron_variant - - - - - - rs4246227 12:25304375 C CCDS31759.2 CCDS31759.2 Transcript intron_variant - - - - - - rs7964388 12:25348539 G - ENSR00000427833 RegulatoryFeature regulatory_region_variant - - - - - - rs7964388 12:25348539 G ENSESTG00000008873 ENSESTT00000022277 Transcript upstream_gene_variant - - - - - - DISTANCE=443 rs7964388 12:25348539 G 55259 NM_018272.3 Transcript upstream_gene_variant - - - - - - DISTANCE=445 rs7964388 12:25348539 G ENSESTG00000008873 ENSESTT00000022296 Transcript upstream_gene_variant - - - - - - DISTANCE=471 rs7964388 12:25348539 G 55259 NM_001204102.1 Transcript upstream_gene_variant - - - - - - DISTANCE=445 rs7964388 12:25348539 G CCDS41762.1 CCDS41762.1 Transcript upstream_gene_variant - - - - - - DISTANCE=527 rs7964388 12:25348539 G ENSESTG00000008873 ENSESTT00000022294 Transcript upstream_gene_variant - - - - - - DISTANCE=471 rs7964388 12:25348539 G CCDS41763.1 CCDS41763.1 Transcript upstream_gene_variant - - - - - - DISTANCE=543 rs7964388 12:25348539 G 144363 NM_001001660.2 Transcript intron_variant - - - - - - rs7964388 12:25348539 G CCDS55811.1 CCDS55811.1 Transcript upstream_gene_variant - - - - - - DISTANCE=527 rs7964388 12:25348539 G 55259 NM_001082973.1 Transcript upstream_gene_variant - - - - - - DISTANCE=445 rs7964388 12:25348539 G 55259 NM_001204101.1 Transcript upstream_gene_variant - - - - - - DISTANCE=445 rs7964388 12:25348539 G ENSESTG00000008873 ENSESTT00000022306 Transcript upstream_gene_variant - - - - - - DISTANCE=479 rs7964388 12:25348539 G ENSESTG00000008873 ENSESTT00000022300 Transcript upstream_gene_variant - - - - - - DISTANCE=475 rs7964388 12:25348539 G 55259 NM_001082972.1 Transcript upstream_gene_variant - - - - - - DISTANCE=445 rs7964388 12:25348539 G CCDS31759.2 CCDS31759.2 Transcript upstream_gene_variant - - - - - - DISTANCE=527 rs2340381 12:25598302 A ENSESTG00000008836 ENSESTT00000022202 Transcript intron_variant - - - - - - rs2340381 12:25598302 A ENSESTG00000008836 ENSESTT00000022186 Transcript intron_variant - - - - - - rs2340381 12:25598302 A ENSESTG00000008836 ENSESTT00000022180 Transcript intron_variant - - - - - - rs2340381 12:25598302 A ENSESTG00000008836 ENSESTT00000022192 Transcript intron_variant - - - - - - rs1705413 12:25670939 G 160492 NM_152590.3 Transcript intron_variant - - - - - - rs1705413 12:25670939 G CCDS44847.1 CCDS44847.1 Transcript intron_variant - - - - - - rs1705413 12:25670939 G 160492 NM_001145728.2 Transcript intron_variant - - - - - - rs1705413 12:25670939 G CCDS44849.1 CCDS44849.1 Transcript intron_variant - - - - - - rs1705413 12:25670939 G CCDS58218.1 CCDS58218.1 Transcript intron_variant - - - - - - rs1705413 12:25670939 G ENSESTG00000008836 ENSESTT00000022186 Transcript intron_variant - - - - - - rs1705413 12:25670939 G CCDS8704.1 CCDS8704.1 Transcript intron_variant - - - - - - rs1705413 12:25670939 G CCDS44848.1 CCDS44848.1 Transcript intron_variant - - - - - - rs1705413 12:25670939 G ENSESTG00000008836 ENSESTT00000022192 Transcript intron_variant - - - - - - rs1705413 12:25670939 G ENSESTG00000008836 ENSESTT00000022202 Transcript intron_variant - - - - - - rs1705413 12:25670939 G 160492 NM_001256266.1 Transcript intron_variant - - - - - - rs1705413 12:25670939 G 160492 NM_001145729.1 Transcript intron_variant - - - - - - rs1705413 12:25670939 G 160492 NM_001145727.2 Transcript intron_variant - - - - - - rs1705413 12:25670939 G ENSESTG00000008836 ENSESTT00000022180 Transcript intron_variant - - - - - - rs1705413 12:25670939 G ENSESTG00000008836 ENSESTT00000022206 Transcript intron_variant - - - - - - rs2729647 12:26245827 T - ENSR00001462186 RegulatoryFeature regulatory_region_variant - - - - - - rs2729647 12:26245827 T - - - intergenic_variant - - - - - - rs7311771 12:26513665 G 3709 NM_002223.2 Transcript intron_variant - - - - - - rs7311771 12:26513665 G CCDS41764.1 CCDS41764.1 Transcript intron_variant - - - - - - rs7311771 12:26513665 G ENSESTG00000016470 ENSESTT00000041302 Transcript intron_variant - - - - - - rs7311771 12:26513665 G ENSESTG00000016582 ENSESTT00000041730 Transcript intron_variant - - - - - - rs10732543 12:26861597 T ENSESTG00000016497 ENSESTT00000041376 Transcript intron_variant - - - - - - rs10732543 12:26861597 T 3709 NM_002223.2 Transcript intron_variant - - - - - - rs10732543 12:26861597 T CCDS41764.1 CCDS41764.1 Transcript intron_variant - - - - - - rs10732543 12:26861597 T ENSESTG00000016497 ENSESTT00000041397 Transcript intron_variant - - - - - - rs10732543 12:26861597 T ENSESTG00000016497 ENSESTT00000041391 Transcript intron_variant - - - - - - rs4963670 12:26935391 C ENSESTG00000016488 ENSESTT00000041342 Transcript intron_variant - - - - - - rs4963670 12:26935391 C 3709 NM_002223.2 Transcript intron_variant - - - - - - rs4963670 12:26935391 C CCDS41764.1 CCDS41764.1 Transcript intron_variant - - - - - - rs4963670 12:26935391 C ENSESTG00000016488 ENSESTT00000041335 Transcript intron_variant - - - - - - rs10842791 12:26935891 C ENSESTG00000016488 ENSESTT00000041342 Transcript intron_variant - - - - - - rs10842791 12:26935891 C 3709 NM_002223.2 Transcript intron_variant - - - - - - rs10842791 12:26935891 C CCDS41764.1 CCDS41764.1 Transcript intron_variant - - - - - - rs10842791 12:26935891 C ENSESTG00000016488 ENSESTT00000041335 Transcript intron_variant - - - - - - rs7314817 12:27497362 A - ENSR00001462307 RegulatoryFeature regulatory_region_variant - - - - - - rs7314817 12:27497362 A CCDS58220.1 CCDS58220.1 Transcript intron_variant - - - - - - rs7314817 12:27497362 A 56938 NM_001248004.1 Transcript intron_variant - - - - - - rs7314817 12:27497362 A ENSESTG00000035545 ENSESTT00000089786 Transcript intron_variant - - - - - - rs7314817 12:27497362 A CCDS8712.1 CCDS8712.1 Transcript intron_variant - - - - - - rs7314817 12:27497362 A 56938 NM_001248005.1 Transcript intron_variant - - - - - - rs7314817 12:27497362 A 56938 NM_001248002.1 Transcript intron_variant - - - - - - rs7314817 12:27497362 A CCDS58222.1 CCDS58222.1 Transcript intron_variant - - - - - - rs7314817 12:27497362 A 56938 NM_001248003.1 Transcript intron_variant - - - - - - rs7314817 12:27497362 A CCDS58219.1 CCDS58219.1 Transcript intron_variant - - - - - - rs7314817 12:27497362 A 56938 NM_020183.4 Transcript intron_variant - - - - - - rs7314817 12:27497362 A CCDS58221.1 CCDS58221.1 Transcript intron_variant - - - - - - rs2126680 12:27729074 C ENSESTG00000028583 ENSESTT00000072013 Transcript intron_variant - - - - - - rs2126680 12:27729074 C ENSESTG00000028583 ENSESTT00000071985 Transcript intron_variant - - - - - - rs2126680 12:27729074 C 8496 NM_001198916.1 Transcript intron_variant - - - - - - rs2126680 12:27729074 C 8496 NM_001198915.1 Transcript intron_variant - - - - - - rs2126680 12:27729074 C ENSESTG00000028583 ENSESTT00000071925 Transcript intron_variant - - - - - - rs2126680 12:27729074 C ENSESTG00000028583 ENSESTT00000071937 Transcript intron_variant - - - - - - rs2126680 12:27729074 C 8496 NM_003622.3 Transcript intron_variant - - - - - - rs2126680 12:27729074 C 8496 NM_177444.2 Transcript intron_variant - - - - - - rs2126680 12:27729074 C ENSESTG00000028583 ENSESTT00000071998 Transcript intron_variant - - - - - - rs2126680 12:27729074 C ENSESTG00000028583 ENSESTT00000071908 Transcript intron_variant - - - - - - rs2162029 12:27823143 C CCDS55812.1 CCDS55812.1 Transcript intron_variant - - - - - - rs2162029 12:27823143 C ENSESTG00000028722 ENSESTT00000072249 Transcript intron_variant - - - - - - rs2162029 12:27823143 C CCDS8713.1 CCDS8713.1 Transcript intron_variant - - - - - - rs2162029 12:27823143 C 8496 NM_001198916.1 Transcript intron_variant - - - - - - rs2162029 12:27823143 C 8496 NM_001198915.1 Transcript intron_variant - - - - - - rs2162029 12:27823143 C ENSESTG00000028583 ENSESTT00000071925 Transcript intron_variant - - - - - - rs2162029 12:27823143 C 8496 NM_003622.3 Transcript intron_variant - - - - - - rs2162029 12:27823143 C 8496 NM_177444.2 Transcript intron_variant - - - - - - rs2162029 12:27823143 C CCDS55813.1 CCDS55813.1 Transcript intron_variant - - - - - - rs2162029 12:27823143 C CCDS55814.1 CCDS55814.1 Transcript intron_variant - - - - - - rs2162029 12:27823143 C ENSESTG00000028583 ENSESTT00000071908 Transcript intron_variant - - - - - - rs2162030 12:27823210 G CCDS55812.1 CCDS55812.1 Transcript intron_variant - - - - - - rs2162030 12:27823210 G ENSESTG00000028722 ENSESTT00000072249 Transcript intron_variant - - - - - - rs2162030 12:27823210 G CCDS8713.1 CCDS8713.1 Transcript intron_variant - - - - - - rs2162030 12:27823210 G 8496 NM_001198916.1 Transcript intron_variant - - - - - - rs2162030 12:27823210 G 8496 NM_001198915.1 Transcript intron_variant - - - - - - rs2162030 12:27823210 G ENSESTG00000028583 ENSESTT00000071925 Transcript intron_variant - - - - - - rs2162030 12:27823210 G 8496 NM_003622.3 Transcript intron_variant - - - - - - rs2162030 12:27823210 G 8496 NM_177444.2 Transcript intron_variant - - - - - - rs2162030 12:27823210 G CCDS55813.1 CCDS55813.1 Transcript intron_variant - - - - - - rs2162030 12:27823210 G CCDS55814.1 CCDS55814.1 Transcript intron_variant - - - - - - rs2162030 12:27823210 G ENSESTG00000028583 ENSESTT00000071908 Transcript intron_variant - - - - - - rs1863222 12:27882238 A CCDS8714.1 CCDS8714.1 Transcript intron_variant - - - - - - rs1863222 12:27882238 A CCDS53769.1 CCDS53769.1 Transcript intron_variant - - - - - - rs1863222 12:27882238 A ENSESTG00000028725 ENSESTT00000072422 Transcript intron_variant - - - - - - rs1863222 12:27882238 A 60488 NM_001190864.1 Transcript intron_variant - - - - - - rs1863222 12:27882238 A 60488 NM_021821.3 Transcript intron_variant - - - - - - rs6487663 12:28281631 C - ENSR00000243265 RegulatoryFeature regulatory_region_variant - - - - - - rs6487663 12:28281631 C - - - intergenic_variant - - - - - - rs7301924 12:28737970 G - - - intergenic_variant - - - - - - rs4329726 12:28770175 A - - - intergenic_variant - - - - - - rs10771437 12:28772832 A - - - intergenic_variant - - - - - - rs7964491 12:28789780 A - - - intergenic_variant - - - - - - rs7979502 12:28789794 G - - - intergenic_variant - - - - - - rs7964724 12:28789976 A - - - intergenic_variant - - - - - - rs4319548 12:28832469 A - - - intergenic_variant - - - - - - rs2725525 12:28850228 A - - - intergenic_variant - - - - - - rs789110 12:28903191 C - - - intergenic_variant - - - - - - rs7132963 12:29126717 C - ENSR00000428390 RegulatoryFeature regulatory_region_variant - - - - - - rs7132963 12:29126717 C - - - intergenic_variant - - - - - - rs10734767 12:29179677 G - ENSR00001462452 RegulatoryFeature regulatory_region_variant - - - - - - rs10734767 12:29179677 G - - - intergenic_variant - - - - - - rs7312297 12:29345109 C ENSESTG00000009451 ENSESTT00000023733 Transcript intron_variant - - - - - - rs299476 12:29705603 T - ENSR00000087607 RegulatoryFeature regulatory_region_variant - - - - - - rs299476 12:29705603 T 83857 NM_175861.3 Transcript intron_variant - - - - - - rs299476 12:29705603 T CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs299476 12:29705603 T ENSESTG00000009514 ENSESTT00000023863 Transcript intron_variant - - - - - - rs299476 12:29705603 T CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs299476 12:29705603 T 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs10843493 12:29855396 C 83857 NM_175861.3 Transcript intron_variant - - - - - - rs10843493 12:29855396 C CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs10843493 12:29855396 C ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs10843493 12:29855396 C CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs10843493 12:29855396 C 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs10843493 12:29855396 C ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs10843493 12:29855396 C ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs10771572 12:29865002 G 83857 NM_175861.3 Transcript intron_variant - - - - - - rs10771572 12:29865002 G CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs10771572 12:29865002 G ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs10771572 12:29865002 G CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs10771572 12:29865002 G 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs10771572 12:29865002 G ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs10771572 12:29865002 G ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs302375 12:29867958 T 83857 NM_175861.3 Transcript intron_variant - - - - - - rs302375 12:29867958 T CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs302375 12:29867958 T ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs302375 12:29867958 T CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs302375 12:29867958 T 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs302375 12:29867958 T ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs302375 12:29867958 T ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs302380 12:29870517 T 83857 NM_175861.3 Transcript intron_variant - - - - - - rs302380 12:29870517 T CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs302380 12:29870517 T ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs302380 12:29870517 T CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs302380 12:29870517 T 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs302380 12:29870517 T ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs302380 12:29870517 T ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs302384 12:29871001 T 83857 NM_175861.3 Transcript intron_variant - - - - - - rs302384 12:29871001 T CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs302384 12:29871001 T ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs302384 12:29871001 T CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs302384 12:29871001 T 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs302384 12:29871001 T ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs302384 12:29871001 T ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs184222 12:29879767 G 83857 NM_175861.3 Transcript intron_variant - - - - - - rs184222 12:29879767 G CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs184222 12:29879767 G ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs184222 12:29879767 G CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs184222 12:29879767 G 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs184222 12:29879767 G ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs184222 12:29879767 G ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs302367 12:29881442 G 83857 NM_175861.3 Transcript intron_variant - - - - - - rs302367 12:29881442 G CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs302367 12:29881442 G ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs302367 12:29881442 G CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs302367 12:29881442 G 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs302367 12:29881442 G ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs302367 12:29881442 G ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs302372 12:29888697 A 83857 NM_175861.3 Transcript intron_variant - - - - - - rs302372 12:29888697 A CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs302372 12:29888697 A ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs302372 12:29888697 A CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs302372 12:29888697 A 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs302372 12:29888697 A ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs302372 12:29888697 A ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs302324 12:29894143 C - ENSR00000428467 RegulatoryFeature regulatory_region_variant - - - - - - rs302324 12:29894143 C 83857 NM_175861.3 Transcript intron_variant - - - - - - rs302324 12:29894143 C CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs302324 12:29894143 C ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs302324 12:29894143 C CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs302324 12:29894143 C 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs302324 12:29894143 C ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs302324 12:29894143 C ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs302325 12:29897451 T 83857 NM_175861.3 Transcript intron_variant - - - - - - rs302325 12:29897451 T CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs302325 12:29897451 T ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs302325 12:29897451 T CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs302325 12:29897451 T 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs302325 12:29897451 T ENSESTG00000009507 ENSESTT00000023837 Transcript intron_variant - - - - - - rs302325 12:29897451 T ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs302363 12:29911926 T 83857 NM_175861.3 Transcript intron_variant - - - - - - rs302363 12:29911926 T CCDS8718.1 CCDS8718.1 Transcript intron_variant - - - - - - rs302363 12:29911926 T ENSESTG00000009507 ENSESTT00000023814 Transcript intron_variant - - - - - - rs302363 12:29911926 T CCDS53772.1 CCDS53772.1 Transcript intron_variant - - - - - - rs302363 12:29911926 T 83857 NM_001193451.1 Transcript intron_variant - - - - - - rs302363 12:29911926 T ENSESTG00000009507 ENSESTT00000023810 Transcript intron_variant - - - - - - rs665883 12:29982202 G - - - intergenic_variant - - - - - - rs302302 12:29984495 C - - - intergenic_variant - - - - - - rs2129139 12:30034394 G - - - intergenic_variant - - - - - - rs10843536 12:30038334 G - ENSR00001462510 RegulatoryFeature regulatory_region_variant - - - - - - rs10843536 12:30038334 G - - - intergenic_variant - - - - - - rs7960359 12:30050591 T - - - intergenic_variant - - - - - - rs7295926 12:30121472 G - - - intergenic_variant - - - - - - rs2647383 12:30137367 C - - - intergenic_variant - - - - - - rs2579031 12:30748862 C - - - intergenic_variant - - - - - - rs33255 12:30906875 T - ENSR00001462555 RegulatoryFeature regulatory_region_variant - - - - - - rs33255 12:30906875 T ENSESTG00000024263 ENSESTT00000061457 Transcript intron_variant - - - - - - rs33255 12:30906875 T 65981 NM_001002259.1 Transcript 5_prime_UTR_variant 574 - - - - - rs33255 12:30906875 T ENSESTG00000024263 ENSESTT00000061410 Transcript intron_variant - - - - - - rs33255 12:30906875 T ENSESTG00000024240 ENSESTT00000061259 Transcript upstream_gene_variant - - - - - - DISTANCE=1133 rs33255 12:30906875 T 65981 NM_001206856.1 Transcript 5_prime_UTR_variant 574 - - - - - rs33255 12:30906875 T 65981 NM_023925.3 Transcript 5_prime_UTR_variant 574 - - - - - rs33255 12:30906875 T CCDS55816.1 CCDS55816.1 Transcript upstream_gene_variant - - - - - - DISTANCE=178 rs33255 12:30906875 T 65981 NR_038177.1 Transcript non_coding_exon_variant,nc_transcript_variant 574 - - - - - rs33255 12:30906875 T ENSESTG00000024263 ENSESTT00000061468 Transcript intron_variant - - - - - - rs33255 12:30906875 T ENSESTG00000024263 ENSESTT00000061392 Transcript intron_variant - - - - - - rs33255 12:30906875 T CCDS8720.1 CCDS8720.1 Transcript upstream_gene_variant - - - - - - DISTANCE=178 rs33255 12:30906875 T 65981 NM_032156.3 Transcript 5_prime_UTR_variant 574 - - - - - rs33255 12:30906875 T CCDS41766.2 CCDS41766.2 Transcript upstream_gene_variant - - - - - - DISTANCE=178 rs35037 12:31174249 C 100506660 NR_038927.1 Transcript non_coding_exon_variant,nc_transcript_variant 1479 - - - - - rs708208 12:31508247 A - - - intergenic_variant - - - - - - rs1144722 12:32326826 C CCDS44859.1 CCDS44859.1 Transcript intron_variant - - - - - - rs1144722 12:32326826 C CCDS8726.1 CCDS8726.1 Transcript intron_variant - - - - - - rs1144722 12:32326826 C 636 NM_001714.2 Transcript intron_variant - - - - - - rs1144722 12:32326826 C ENSESTG00000011373 ENSESTT00000028571 Transcript intron_variant - - - - - - rs1144722 12:32326826 C ENSESTG00000011373 ENSESTT00000028568 Transcript intron_variant - - - - - - rs1144722 12:32326826 C 636 NM_001003398.1 Transcript intron_variant - - - - - - rs1144724 12:32332132 T CCDS44859.1 CCDS44859.1 Transcript intron_variant - - - - - - rs1144724 12:32332132 T CCDS8726.1 CCDS8726.1 Transcript intron_variant - - - - - - rs1144724 12:32332132 T 636 NM_001714.2 Transcript intron_variant - - - - - - rs1144724 12:32332132 T ENSESTG00000011373 ENSESTT00000028571 Transcript intron_variant - - - - - - rs1144724 12:32332132 T ENSESTG00000011373 ENSESTT00000028568 Transcript intron_variant - - - - - - rs1144724 12:32332132 T 636 NM_001003398.1 Transcript intron_variant - - - - - - rs1798593 12:32334701 A CCDS44859.1 CCDS44859.1 Transcript intron_variant - - - - - - rs1798593 12:32334701 A CCDS8726.1 CCDS8726.1 Transcript intron_variant - - - - - - rs1798593 12:32334701 A 636 NM_001714.2 Transcript intron_variant - - - - - - rs1798593 12:32334701 A ENSESTG00000011373 ENSESTT00000028571 Transcript intron_variant - - - - - - rs1798593 12:32334701 A ENSESTG00000011373 ENSESTT00000028568 Transcript intron_variant - - - - - - rs1798593 12:32334701 A 636 NM_001003398.1 Transcript intron_variant - - - - - - rs2632343 12:32545559 C - - - intergenic_variant - - - - - - rs7975077 12:32981958 C CCDS31771.1 CCDS31771.1 Transcript intron_variant - - - - - - rs7975077 12:32981958 C 5318 NM_004572.3 Transcript intron_variant - - - - - - rs7975077 12:32981958 C ENSESTG00000011753 ENSESTT00000029500 Transcript upstream_gene_variant - - - - - - DISTANCE=4861 rs7975077 12:32981958 C 5318 NM_001005242.2 Transcript intron_variant - - - - - - rs7975077 12:32981958 C CCDS8731.1 CCDS8731.1 Transcript intron_variant - - - - - - rs7975077 12:32981958 C ENSESTG00000000474 ENSESTT00000001244 Transcript upstream_gene_variant - - - - - - DISTANCE=4619 rs7975077 12:32981958 C ENSESTG00000000474 ENSESTT00000001224 Transcript intron_variant - - - - - - rs10772054 12:33376030 T - - - intergenic_variant - - - - - - rs10734812 12:34361435 C ENSESTG00000019132 ENSESTT00000048099 Transcript downstream_gene_variant - - - - - - DISTANCE=3374 rs10743863 12:34734928 C - - - intergenic_variant - - - - - - rs10879291 12:38197044 C - - - intergenic_variant - - - - - - rs7967069 12:38736483 A - - - intergenic_variant - - - - - - rs826859 12:39140537 C CCDS8733.1 CCDS8733.1 Transcript intron_variant - - - - - - rs826859 12:39140537 C 144402 NM_153634.2 Transcript intron_variant - - - - - - rs826859 12:39140537 C ENSESTG00000028882 ENSESTT00000072817 Transcript intron_variant - - - - - - rs4768607 12:39565180 A - - - intergenic_variant - - - - - - rs4316571 12:40240700 G ENSESTG00000035233 ENSESTT00000089017 Transcript intron_variant - - - - - - rs4316571 12:40240700 G ENSESTG00000035233 ENSESTT00000089019 Transcript intron_variant - - - - - - rs4316571 12:40240700 G ENSESTG00000035233 ENSESTT00000089012 Transcript intron_variant - - - - - - rs4316571 12:40240700 G 114134 NM_052885.3 Transcript intron_variant - - - - - - rs4316571 12:40240700 G ENSESTG00000035233 ENSESTT00000089011 Transcript intron_variant - - - - - - rs4316571 12:40240700 G CCDS8736.2 CCDS8736.2 Transcript intron_variant - - - - - - rs499072 12:40367008 C ENSESTG00000035233 ENSESTT00000089017 Transcript intron_variant - - - - - - rs499072 12:40367008 C ENSESTG00000035233 ENSESTT00000089014 Transcript intron_variant - - - - - - rs499072 12:40367008 C ENSESTG00000035233 ENSESTT00000089019 Transcript intron_variant - - - - - - rs499072 12:40367008 C ENSESTG00000035233 ENSESTT00000089012 Transcript intron_variant - - - - - - rs499072 12:40367008 C 114134 NM_052885.3 Transcript intron_variant - - - - - - rs499072 12:40367008 C ENSESTG00000035233 ENSESTT00000089011 Transcript intron_variant - - - - - - rs499072 12:40367008 C CCDS8736.2 CCDS8736.2 Transcript intron_variant - - - - - - rs10735941 12:40845444 A 283463 XM_003846356.1 Transcript intron_variant - - - - - - rs10784794 12:41099013 C 1272 NM_001256063.1 Transcript intron_variant - - - - - - rs10784794 12:41099013 C 1272 NM_001843.3 Transcript intron_variant - - - - - - rs690709 12:41499792 G - - - intergenic_variant - - - - - - rs1431119 12:41635395 C CCDS53777.1 CCDS53777.1 Transcript intron_variant - - - - - - rs1431119 12:41635395 C 29951 NM_001164595.1 Transcript intron_variant - - - - - - rs287029 12:41986385 G - - - intergenic_variant - - - - - - rs2730981 12:43196781 C - ENSR00001462904 RegulatoryFeature regulatory_region_variant - - - - - - rs2730981 12:43196781 C - - - intergenic_variant - - - - - - rs2706323 12:43551033 A - - - intergenic_variant - - - - - - rs1567460 12:43857579 G CCDS31778.2 CCDS31778.2 Transcript intron_variant - - - - - - rs1567460 12:43857579 G 80070 NM_025003.3 Transcript intron_variant - - - - - - rs7968448 12:43961465 T - - - intergenic_variant - - - - - - rs166733 12:44027961 G - - - intergenic_variant - - - - - - rs393659 12:44039212 T - - - intergenic_variant - - - - - - rs277218 12:44064661 G - - - intergenic_variant - - - - - - rs1534806 12:44263402 T CCDS8745.1 CCDS8745.1 Transcript intron_variant - - - - - - rs1534806 12:44263402 T ENSESTG00000007106 ENSESTT00000017970 Transcript intron_variant - - - - - - rs1534806 12:44263402 T 84216 NM_032256.1 Transcript intron_variant - - - - - - rs1320920 12:44267588 C CCDS8745.1 CCDS8745.1 Transcript intron_variant - - - - - - rs1320920 12:44267588 C ENSESTG00000007106 ENSESTT00000017970 Transcript intron_variant - - - - - - rs1320920 12:44267588 C 84216 NM_032256.1 Transcript intron_variant - - - - - - rs1726899 12:44598050 C CCDS8745.1 CCDS8745.1 Transcript intron_variant - - - - - - rs1726899 12:44598050 C ENSESTG00000007116 ENSESTT00000017994 Transcript intron_variant - - - - - - rs1726899 12:44598050 C 84216 NM_032256.1 Transcript intron_variant - - - - - - rs1726894 12:44762636 C CCDS8745.1 CCDS8745.1 Transcript intron_variant - - - - - - rs1726894 12:44762636 C 84216 NM_032256.1 Transcript intron_variant - - - - - - rs642824 12:45117631 C 4753 NM_001145107.1 Transcript intron_variant - - - - - - rs642824 12:45117631 C ENSESTG00000023523 ENSESTT00000059678 Transcript intron_variant - - - - - - rs642824 12:45117631 C ENSESTG00000023523 ENSESTT00000059669 Transcript intron_variant - - - - - - rs642824 12:45117631 C 4753 NM_006159.2 Transcript intron_variant - - - - - - rs642824 12:45117631 C CCDS8746.1 CCDS8746.1 Transcript intron_variant - - - - - - rs642824 12:45117631 C 4753 NM_001145109.1 Transcript intron_variant - - - - - - rs642824 12:45117631 C 4753 NM_001145108.1 Transcript intron_variant - - - - - - rs642824 12:45117631 C CCDS44863.1 CCDS44863.1 Transcript intron_variant - - - - - - rs642824 12:45117631 C 4753 NM_001145110.1 Transcript intron_variant - - - - - - rs642824 12:45117631 C CCDS44864.1 CCDS44864.1 Transcript intron_variant - - - - - - rs642824 12:45117631 C CCDS53781.1 CCDS53781.1 Transcript intron_variant - - - - - - rs1390036 12:45437144 A 440097 NM_001004329.2 Transcript intron_variant - - - - - - rs1390036 12:45437144 A CCDS31781.1 CCDS31781.1 Transcript intron_variant - - - - - - rs10748431 12:46080504 G - - - intergenic_variant - - - - - - rs6582572 12:46193778 G CCDS31783.1 CCDS31783.1 Transcript intron_variant - - - - - - rs6582572 12:46193778 G ENSESTG00000014963 ENSESTT00000037486 Transcript intron_variant - - - - - - rs6582572 12:46193778 G 196528 NM_152641.2 Transcript intron_variant - - - - - - rs7968437 12:46430990 G - - - intergenic_variant - - - - - - rs7312523 12:46442107 G - - - intergenic_variant - - - - - - rs10748445 12:46670762 C - ENSR00001463077 RegulatoryFeature regulatory_region_variant - - - - - - rs10748445 12:46670762 C - - - intergenic_variant - - - - - - rs7310704 12:46946449 C ENSESTG00000015015 ENSESTT00000037651 Transcript intron_variant - - - - - - rs7310704 12:46946449 C ENSESTG00000015015 ENSESTT00000037637 Transcript intron_variant - - - - - - rs7310704 12:46946449 C ENSESTG00000015015 ENSESTT00000037647 Transcript intron_variant - - - - - - rs7310704 12:46946449 C ENSESTG00000015015 ENSESTT00000037630 Transcript intron_variant - - - - - - rs12367013 12:47140691 T - - - intergenic_variant - - - - - - rs2522266 12:47396001 A - - - intergenic_variant - - - - - - rs2711711 12:47414398 C - ENSR00001463168 RegulatoryFeature regulatory_region_variant - - - - - - rs2711711 12:47414398 C - - - intergenic_variant - - - - - - rs7297706 12:47433354 G - - - intergenic_variant - - - - - - rs854896 12:47488066 A - - - intergenic_variant - - - - - - rs2188904 12:47796096 A - - - intergenic_variant - - - - - - rs624813 12:48018637 C - - - intergenic_variant - - - - - - rs2956701 12:48691569 A - - - intergenic_variant - - - - - - rs6580691 12:49051668 G 677793 NR_002950.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1103 rs6580691 12:49051668 G ENSESTG00000011328 ENSESTT00000028490 Transcript intron_variant - - - - - - rs6580691 12:49051668 G 54934 NM_017822.3 Transcript intron_variant - - - - - - rs6580691 12:49051668 G CCDS44869.1 CCDS44869.1 Transcript intron_variant - - - - - - rs6580691 12:49051668 G ENSESTG00000011328 ENSESTT00000028495 Transcript intron_variant - - - - - - rs6580691 12:49051668 G 677815 NR_002968.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3367 rs7301480 12:49139858 A 255411 NR_029449.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7301480 12:49139858 A ENSESTG00000010435 ENSESTT00000026133 Transcript intron_variant - - - - - - rs7301480 12:49139858 A 255411 NR_029448.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2720306 12:50151746 C ENSESTG00000034820 ENSESTT00000088025 Transcript intron_variant - - - - - - rs2720306 12:50151746 C 7009 NM_003217.2 Transcript intron_variant - - - - - - rs2720306 12:50151746 C CCDS31797.1 CCDS31797.1 Transcript intron_variant - - - - - - rs2720306 12:50151746 C ENSESTG00000034820 ENSESTT00000088083 Transcript intron_variant - - - - - - rs2720306 12:50151746 C ENSESTG00000034820 ENSESTT00000088028 Transcript downstream_gene_variant - - - - - - DISTANCE=2207 rs2720306 12:50151746 C CCDS44875.1 CCDS44875.1 Transcript intron_variant - - - - - - rs2720306 12:50151746 C 7009 NM_001098576.1 Transcript intron_variant - - - - - - rs10083073 12:50781716 C ENSESTG00000034989 ENSESTT00000088428 Transcript intron_variant - - - - - - rs10083073 12:50781716 C CCDS44878.1 CCDS44878.1 Transcript intron_variant - - - - - - rs10083073 12:50781716 C 121006 NM_001145475.1 Transcript intron_variant - - - - - - rs829113 12:51205306 C ENSESTG00000003511 ENSESTT00000008766 Transcript downstream_gene_variant - - - - - - DISTANCE=1935 rs829113 12:51205306 C ENSESTG00000003511 ENSESTT00000008763 Transcript intron_variant - - - - - - rs829113 12:51205306 C ENSESTG00000003511 ENSESTT00000008770 Transcript intron_variant - - - - - - rs829113 12:51205306 C 466 NM_005171.4 Transcript intron_variant - - - - - - rs829113 12:51205306 C CCDS8803.1 CCDS8803.1 Transcript intron_variant - - - - - - rs4768956 12:51461425 G 81566 NM_030809.2 Transcript intron_variant - - - - - - rs4768956 12:51461425 G 81566 NR_045072.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4768956 12:51461425 G CCDS8807.1 CCDS8807.1 Transcript intron_variant - - - - - - rs2640513 12:51526034 G - ENSR00000244067 RegulatoryFeature regulatory_region_variant - - - - - - rs2640513 12:51526034 G CCDS55827.1 CCDS55827.1 Transcript intron_variant - - - - - - rs2640513 12:51526034 G 7024 NM_005653.4 Transcript intron_variant - - - - - - rs2640513 12:51526034 G ENSESTG00000003905 ENSESTT00000009877 Transcript intron_variant - - - - - - rs2640513 12:51526034 G 7024 NM_001173453.1 Transcript intron_variant - - - - - - rs2640513 12:51526034 G ENSESTG00000003905 ENSESTT00000009898 Transcript intron_variant - - - - - - rs2640513 12:51526034 G 7024 NM_001173452.1 Transcript intron_variant - - - - - - rs2640513 12:51526034 G ENSESTG00000003905 ENSESTT00000009886 Transcript intron_variant - - - - - - rs2640513 12:51526034 G CCDS8808.1 CCDS8808.1 Transcript intron_variant - - - - - - rs6580832 12:51801544 G 9498 NM_001258401.2 Transcript intron_variant - - - - - - rs6580832 12:51801544 G 9498 NM_001267615.1 Transcript intron_variant - - - - - - rs10876179 12:51821653 G CCDS44890.1 CCDS44890.1 Transcript intron_variant - - - - - - rs10876179 12:51821653 G 9498 NM_001039960.2 Transcript intron_variant - - - - - - rs10876179 12:51821653 G ENSESTG00000003655 ENSESTT00000009174 Transcript intron_variant - - - - - - rs10876179 12:51821653 G 9498 NM_001258401.2 Transcript intron_variant - - - - - - rs10876179 12:51821653 G 9498 NM_001267615.1 Transcript intron_variant - - - - - - rs10876179 12:51821653 G 9498 NR_047672.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10876179 12:51821653 G ENSESTG00000003655 ENSESTT00000009167 Transcript intron_variant - - - - - - rs10876179 12:51821653 G 9498 NM_001258403.1 Transcript intron_variant - - - - - - rs10876179 12:51821653 G 9498 NM_001258402.1 Transcript intron_variant - - - - - - rs7296891 12:51823626 A CCDS44890.1 CCDS44890.1 Transcript intron_variant - - - - - - rs7296891 12:51823626 A 9498 NM_001039960.2 Transcript intron_variant - - - - - - rs7296891 12:51823626 A ENSESTG00000003655 ENSESTT00000009174 Transcript intron_variant - - - - - - rs7296891 12:51823626 A 9498 NM_001258401.2 Transcript intron_variant - - - - - - rs7296891 12:51823626 A 9498 NM_001267615.1 Transcript intron_variant - - - - - - rs7296891 12:51823626 A 9498 NR_047672.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7296891 12:51823626 A ENSESTG00000003655 ENSESTT00000009167 Transcript intron_variant - - - - - - rs7296891 12:51823626 A 9498 NM_001258403.1 Transcript intron_variant - - - - - - rs7296891 12:51823626 A 9498 NM_001258402.1 Transcript intron_variant - - - - - - rs7964235 12:51836271 G - ENSR00001463492 RegulatoryFeature regulatory_region_variant - - - - - - rs7964235 12:51836271 G CCDS44890.1 CCDS44890.1 Transcript intron_variant - - - - - - rs7964235 12:51836271 G 9498 NM_001039960.2 Transcript intron_variant - - - - - - rs7964235 12:51836271 G ENSESTG00000003655 ENSESTT00000009174 Transcript downstream_gene_variant - - - - - - DISTANCE=1317 rs7964235 12:51836271 G 9498 NM_001258401.2 Transcript intron_variant - - - - - - rs7964235 12:51836271 G 9498 NM_001267615.1 Transcript intron_variant - - - - - - rs7964235 12:51836271 G 9498 NR_047672.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1308 rs7964235 12:51836271 G ENSESTG00000003655 ENSESTT00000009167 Transcript intron_variant - - - - - - rs7964235 12:51836271 G 9498 NM_001258403.1 Transcript intron_variant - - - - - - rs7964235 12:51836271 G 9498 NM_001258402.1 Transcript intron_variant - - - - - - rs1389196 12:51926714 T - - - intergenic_variant - - - - - - rs706832 12:52284233 C ENSESTG00000024930 ENSESTT00000063004 Transcript upstream_gene_variant - - - - - - DISTANCE=91 rs706832 12:52284233 C CCDS44892.1 CCDS44892.1 Transcript intron_variant - - - - - - rs706832 12:52284233 C ENSESTG00000024930 ENSESTT00000062960 Transcript downstream_gene_variant - - - - - - DISTANCE=1004 rs706832 12:52284233 C CCDS8815.1 CCDS8815.1 Transcript intron_variant - - - - - - rs706832 12:52284233 C ENSESTG00000024930 ENSESTT00000062944 Transcript intron_variant - - - - - - rs706832 12:52284233 C 341405 NM_182608.3 Transcript intron_variant - - - - - - rs706832 12:52284233 C 341405 NM_001130015.1 Transcript intron_variant - - - - - - rs706832 12:52284233 C ENSESTG00000024930 ENSESTT00000062971 Transcript downstream_gene_variant - - - - - - DISTANCE=1546 rs808873 12:52348182 T 91 NM_004302.4 Transcript intron_variant - - - - - - rs808873 12:52348182 T ENSESTG00000025068 ENSESTT00000063418 Transcript intron_variant - - - - - - rs808873 12:52348182 T ENSESTG00000025068 ENSESTT00000063447 Transcript intron_variant - - - - - - rs808873 12:52348182 T ENSESTG00000025068 ENSESTT00000063455 Transcript intron_variant - - - - - - rs808873 12:52348182 T 91 NM_020327.3 Transcript intron_variant - - - - - - rs808873 12:52348182 T 91 NM_020328.3 Transcript intron_variant - - - - - - rs808873 12:52348182 T CCDS44894.2 CCDS44894.2 Transcript intron_variant - - - - - - rs808873 12:52348182 T CCDS8816.1 CCDS8816.1 Transcript intron_variant - - - - - - rs3847856 12:52533094 C - - - intergenic_variant - - - - - - rs2254766 12:52836841 G - ENSR00000430673 RegulatoryFeature regulatory_region_variant - - - - - - rs2254766 12:52836841 G 3854 NM_005555.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3594 rs2254766 12:52836841 G ENSESTG00000025889 ENSESTT00000066171 Transcript downstream_gene_variant - - - - - - DISTANCE=4049 rs2254766 12:52836841 G CCDS8828.1 CCDS8828.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4133 rs2254766 12:52836841 G ENSESTG00000025889 ENSESTT00000066138 Transcript downstream_gene_variant - - - - - - DISTANCE=4049 rs2254766 12:52836841 G ENSESTG00000025889 ENSESTT00000066225 Transcript downstream_gene_variant - - - - - - DISTANCE=4049 rs2254766 12:52836841 G ENSESTG00000025889 ENSESTT00000066188 Transcript downstream_gene_variant - - - - - - DISTANCE=3658 rs2254766 12:52836841 G ENSESTG00000025889 ENSESTT00000065808 Transcript downstream_gene_variant - - - - - - DISTANCE=4282 rs830369 12:52933194 G - ENSR00001463614 RegulatoryFeature regulatory_region_variant - - - - - - rs830369 12:52933194 G ENSESTG00000025889 ENSESTT00000065849 Transcript intron_variant - - - - - - rs830369 12:52933194 G ENSESTG00000025889 ENSESTT00000065416 Transcript intron_variant - - - - - - rs830369 12:52933194 G 112802 NM_033448.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4499 rs866135 12:53058971 T ENSESTG00000025889 ENSESTT00000065416 Transcript intron_variant - - - - - - rs828108 12:53063496 C ENSESTG00000025889 ENSESTT00000065416 Transcript intron_variant - - - - - - rs591451 12:53118979 C ENSESTG00000015451 ENSESTT00000038742 Transcript downstream_gene_variant - - - - - - DISTANCE=4336 rs591451 12:53118979 C ENSESTG00000015451 ENSESTT00000038784 Transcript downstream_gene_variant - - - - - - DISTANCE=4336 rs591451 12:53118979 C ENSESTG00000015603 ENSESTT00000039121 Transcript intron_variant - - - - - - rs12366825 12:53369662 C ENSESTG00000014401 ENSESTT00000036098 Transcript intron_variant - - - - - - rs711314 12:53490424 C - ENSR00001463640 RegulatoryFeature regulatory_region_variant - - - - - - rs711314 12:53490424 C ENSESTG00000014615 ENSESTT00000036593 Transcript upstream_gene_variant - - - - - - DISTANCE=1025 rs711314 12:53490424 C ENSESTG00000014401 ENSESTT00000036098 Transcript intron_variant - - - - - - rs711314 12:53490424 C ENSESTG00000014615 ENSESTT00000036589 Transcript upstream_gene_variant - - - - - - DISTANCE=997 rs711314 12:53490424 C CCDS8846.1 CCDS8846.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1078 rs711314 12:53490424 C 3489 NM_002178.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1012 rs4622317 12:53863872 A CCDS44901.1 CCDS44901.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A CCDS44904.1 CCDS44904.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A 5094 NM_001098620.2 Transcript intron_variant - - - - - - rs4622317 12:53863872 A ENSESTG00000014914 ENSESTT00000037483 Transcript intron_variant - - - - - - rs4622317 12:53863872 A ENSESTG00000014914 ENSESTT00000037448 Transcript intron_variant - - - - - - rs4622317 12:53863872 A 5094 NM_001128913.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A CCDS55830.1 CCDS55830.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A ENSESTG00000014914 ENSESTT00000037501 Transcript intron_variant - - - - - - rs4622317 12:53863872 A 5094 NM_031989.4 Transcript intron_variant - - - - - - rs4622317 12:53863872 A ENSESTG00000014914 ENSESTT00000037445 Transcript intron_variant - - - - - - rs4622317 12:53863872 A CCDS44900.1 CCDS44900.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A 5094 NM_005016.5 Transcript intron_variant - - - - - - rs4622317 12:53863872 A 5094 NM_001128912.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A ENSESTG00000014914 ENSESTT00000037511 Transcript intron_variant - - - - - - rs4622317 12:53863872 A CCDS8859.1 CCDS8859.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A ENSESTG00000014914 ENSESTT00000037544 Transcript downstream_gene_variant - - - - - - DISTANCE=2236 rs4622317 12:53863872 A 5094 NM_001128914.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A ENSESTG00000014914 ENSESTT00000037506 Transcript intron_variant - - - - - - rs4622317 12:53863872 A CCDS44903.1 CCDS44903.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A CCDS44902.1 CCDS44902.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A 5094 NM_001128911.1 Transcript intron_variant - - - - - - rs4622317 12:53863872 A ENSESTG00000014914 ENSESTT00000037491 Transcript intron_variant - - - - - - rs10747681 12:54196900 G - - - intergenic_variant - - - - - - rs2586700 12:54286531 G - - - intergenic_variant - - - - - - rs1249384 12:54898537 G ENSESTG00000005623 ENSESTT00000014423 Transcript intron_variant - - - - - - rs1249384 12:54898537 G CCDS53799.1 CCDS53799.1 Transcript intron_variant - - - - - - rs1249384 12:54898537 G ENSESTG00000005623 ENSESTT00000014436 Transcript intron_variant - - - - - - rs1249384 12:54898537 G ENSESTG00000005623 ENSESTT00000014416 Transcript intron_variant - - - - - - rs1249384 12:54898537 G 3071 NM_001184976.1 Transcript intron_variant - - - - - - rs1249384 12:54898537 G ENSESTG00000005623 ENSESTT00000014434 Transcript intron_variant - - - - - - rs1249384 12:54898537 G ENSESTG00000005623 ENSESTT00000014430 Transcript intron_variant - - - - - - rs1249384 12:54898537 G 3071 NM_005337.4 Transcript intron_variant - - - - - - rs1249384 12:54898537 G ENSESTG00000005623 ENSESTT00000014427 Transcript downstream_gene_variant - - - - - - DISTANCE=3823 rs1249384 12:54898537 G ENSESTG00000005623 ENSESTT00000014407 Transcript intron_variant - - - - - - rs1249384 12:54898537 G CCDS31813.1 CCDS31813.1 Transcript intron_variant - - - - - - rs1249381 12:54900012 C - ENSR00001463757 RegulatoryFeature regulatory_region_variant - - - - - - rs1249381 12:54900012 C ENSESTG00000005623 ENSESTT00000014423 Transcript intron_variant - - - - - - rs1249381 12:54900012 C CCDS53799.1 CCDS53799.1 Transcript intron_variant - - - - - - rs1249381 12:54900012 C ENSESTG00000005623 ENSESTT00000014436 Transcript intron_variant - - - - - - rs1249381 12:54900012 C ENSESTG00000005623 ENSESTT00000014416 Transcript intron_variant - - - - - - rs1249381 12:54900012 C 3071 NM_001184976.1 Transcript intron_variant - - - - - - rs1249381 12:54900012 C ENSESTG00000005623 ENSESTT00000014434 Transcript intron_variant - - - - - - rs1249381 12:54900012 C ENSESTG00000005623 ENSESTT00000014430 Transcript intron_variant - - - - - - rs1249381 12:54900012 C 3071 NM_005337.4 Transcript intron_variant - - - - - - rs1249381 12:54900012 C ENSESTG00000005623 ENSESTT00000014407 Transcript intron_variant - - - - - - rs1249381 12:54900012 C CCDS31813.1 CCDS31813.1 Transcript intron_variant - - - - - - rs2706261 12:54913549 C ENSESTG00000005623 ENSESTT00000014423 Transcript downstream_gene_variant - - - - - - DISTANCE=2122 rs2706261 12:54913549 C CCDS53799.1 CCDS53799.1 Transcript intron_variant - - - - - - rs2706261 12:54913549 C ENSESTG00000005623 ENSESTT00000014436 Transcript downstream_gene_variant - - - - - - DISTANCE=2122 rs2706261 12:54913549 C ENSESTG00000005623 ENSESTT00000014416 Transcript intron_variant - - - - - - rs2706261 12:54913549 C 3071 NM_001184976.1 Transcript intron_variant - - - - - - rs2706261 12:54913549 C ENSESTG00000005623 ENSESTT00000014434 Transcript intron_variant - - - - - - rs2706261 12:54913549 C ENSESTG00000005623 ENSESTT00000014430 Transcript intron_variant - - - - - - rs2706261 12:54913549 C 3071 NM_005337.4 Transcript intron_variant - - - - - - rs2706261 12:54913549 C ENSESTG00000005623 ENSESTT00000014407 Transcript intron_variant - - - - - - rs2706261 12:54913549 C CCDS31813.1 CCDS31813.1 Transcript intron_variant - - - - - - rs10747697 12:54925750 C CCDS53799.1 CCDS53799.1 Transcript intron_variant - - - - - - rs10747697 12:54925750 C ENSESTG00000005623 ENSESTT00000014416 Transcript intron_variant - - - - - - rs10747697 12:54925750 C 3071 NM_001184976.1 Transcript intron_variant - - - - - - rs10747697 12:54925750 C ENSESTG00000005623 ENSESTT00000014434 Transcript intron_variant - - - - - - rs10747697 12:54925750 C ENSESTG00000005623 ENSESTT00000014430 Transcript intron_variant - - - - - - rs10747697 12:54925750 C 3071 NM_005337.4 Transcript intron_variant - - - - - - rs10747697 12:54925750 C ENSESTG00000005623 ENSESTT00000014407 Transcript intron_variant - - - - - - rs10747697 12:54925750 C CCDS31813.1 CCDS31813.1 Transcript intron_variant - - - - - - rs1153140 12:54973623 C - ENSR00000088716 RegulatoryFeature regulatory_region_variant - - - - - - rs1153140 12:54973623 C ENSESTG00000007962 ENSESTT00000020208 Transcript downstream_gene_variant - - - - - - DISTANCE=4620 rs1153140 12:54973623 C ENSESTG00000008114 ENSESTT00000020525 Transcript downstream_gene_variant - - - - - - DISTANCE=388 rs1153140 12:54973623 C 5502 NM_006741.3 Transcript 3_prime_UTR_variant 1235 - - - - - rs1153140 12:54973623 C ENSESTG00000007962 ENSESTT00000020202 Transcript downstream_gene_variant - - - - - - DISTANCE=1545 rs1153140 12:54973623 C CCDS53800.1 CCDS53800.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2511 rs1153140 12:54973623 C 5153 NM_000924.3 Transcript downstream_gene_variant - - - - - - DISTANCE=600 rs1153140 12:54973623 C ENSESTG00000007962 ENSESTT00000020176 Transcript downstream_gene_variant - - - - - - DISTANCE=4620 rs1153140 12:54973623 C ENSESTG00000007962 ENSESTT00000020211 Transcript downstream_gene_variant - - - - - - DISTANCE=1545 rs1153140 12:54973623 C ENSESTG00000007962 ENSESTT00000020213 Transcript downstream_gene_variant - - - - - - DISTANCE=1545 rs1153140 12:54973623 C ENSESTG00000007962 ENSESTT00000020167 Transcript downstream_gene_variant - - - - - - DISTANCE=1545 rs1153140 12:54973623 C CCDS8882.1 CCDS8882.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2511 rs1153140 12:54973623 C 5153 NM_001165975.2 Transcript downstream_gene_variant - - - - - - DISTANCE=600 rs1153140 12:54973623 C CCDS44912.1 CCDS44912.1 Transcript downstream_gene_variant - - - - - - DISTANCE=548 rs1153140 12:54973623 C ENSESTG00000007962 ENSESTT00000020219 Transcript downstream_gene_variant - - - - - - DISTANCE=600 rs1153140 12:54973623 C ENSESTG00000007962 ENSESTT00000020118 Transcript downstream_gene_variant - - - - - - DISTANCE=4620 rs1153140 12:54973623 C ENSESTG00000008114 ENSESTT00000020518 Transcript downstream_gene_variant - - - - - - DISTANCE=421 rs1153161 12:55068345 G - - - intergenic_variant - - - - - - rs11171089 12:55201646 A - - - intergenic_variant - - - - - - rs2444848 12:55256750 T 118430 NM_058173.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4573 rs2444848 12:55256750 T CCDS8885.1 CCDS8885.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4724 rs2444848 12:55256750 T ENSESTG00000008009 ENSESTT00000020275 Transcript downstream_gene_variant - - - - - - DISTANCE=4583 rs2444848 12:55256750 T ENSESTG00000008009 ENSESTT00000020260 Transcript downstream_gene_variant - - - - - - DISTANCE=4580 rs10747735 12:55485600 T - - - intergenic_variant - - - - - - rs10747753 12:55797451 A 403282 NM_001005518.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2200 rs10747753 12:55797451 A CCDS31821.1 CCDS31821.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2200 rs6581063 12:55907277 T ENSESTG00000008036 ENSESTT00000020303 Transcript intron_variant - - - - - - rs7977235 12:55910986 C ENSESTG00000008036 ENSESTT00000020303 Transcript intron_variant - - - - - - rs1274499 12:56660411 C - ENSR00000244426 RegulatoryFeature regulatory_region_variant - - - - - - rs1274499 12:56660411 C ENSESTG00000007082 ENSESTT00000017913 Transcript intron_variant - - - - - - rs1274499 12:56660411 C ENSESTG00000007380 ENSESTT00000018616 Transcript upstream_gene_variant - - - - - - DISTANCE=2153 rs1274499 12:56660411 C 93058 NM_001099337.1 Transcript upstream_gene_variant - - - - - - DISTANCE=656 rs1274499 12:56660411 C 93058 NM_144576.3 Transcript upstream_gene_variant - - - - - - DISTANCE=231 rs1274499 12:56660411 C ENSESTG00000007380 ENSESTT00000018613 Transcript upstream_gene_variant - - - - - - DISTANCE=658 rs1274499 12:56660411 C CCDS44921.1 CCDS44921.1 Transcript upstream_gene_variant - - - - - - DISTANCE=769 rs1274499 12:56660411 C CCDS41796.1 CCDS41796.1 Transcript upstream_gene_variant - - - - - - DISTANCE=492 rs1274499 12:56660411 C ENSESTG00000007380 ENSESTT00000018604 Transcript upstream_gene_variant - - - - - - DISTANCE=657 rs703847 12:57438423 C ENSESTG00000004884 ENSESTT00000012416 Transcript downstream_gene_variant - - - - - - DISTANCE=3024 rs703847 12:57438423 C 4640 NM_001256041.1 Transcript intron_variant - - - - - - rs703847 12:57438423 C 4640 NM_005379.3 Transcript intron_variant - - - - - - rs703847 12:57438423 C ENSESTG00000004892 ENSESTT00000012444 Transcript intron_variant - - - - - - rs703847 12:57438423 C ENSESTG00000004892 ENSESTT00000012450 Transcript upstream_gene_variant - - - - - - DISTANCE=3166 rs703847 12:57438423 C CCDS8929.1 CCDS8929.1 Transcript intron_variant - - - - - - rs703847 12:57438423 C ENSESTG00000004884 ENSESTT00000012411 Transcript downstream_gene_variant - - - - - - DISTANCE=3292 rs6581144 12:57808834 G ENSESTG00000004782 ENSESTT00000012166 Transcript intron_variant - - - - - - rs6581144 12:57808834 G ENSESTG00000004782 ENSESTT00000012160 Transcript intron_variant - - - - - - rs6581144 12:57808834 G ENSESTG00000004782 ENSESTT00000012164 Transcript intron_variant - - - - - - rs524522 12:57869500 C CCDS44928.1 CCDS44928.1 Transcript intron_variant - - - - - - rs524522 12:57869500 C 64333 NM_001080156.1 Transcript intron_variant - - - - - - rs524522 12:57869500 C 2735 NM_001167609.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3449 rs524522 12:57869500 C CCDS8941.2 CCDS8941.2 Transcript intron_variant - - - - - - rs524522 12:57869500 C 2735 NM_001160045.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3449 rs524522 12:57869500 C ENSESTG00000004590 ENSESTT00000011578 Transcript downstream_gene_variant - - - - - - DISTANCE=4915 rs524522 12:57869500 C ENSESTG00000004590 ENSESTT00000011589 Transcript downstream_gene_variant - - - - - - DISTANCE=4715 rs524522 12:57869500 C 64333 NM_032496.2 Transcript intron_variant - - - - - - rs524522 12:57869500 C CCDS44929.1 CCDS44929.1 Transcript intron_variant - - - - - - rs524522 12:57869500 C ENSESTG00000004601 ENSESTT00000011600 Transcript intron_variant - - - - - - rs524522 12:57869500 C 2735 NM_005269.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3449 rs524522 12:57869500 C 64333 NM_001080157.1 Transcript intron_variant - - - - - - rs524522 12:57869500 C CCDS8940.1 CCDS8940.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3656 rs524522 12:57869500 C ENSESTG00000004771 ENSESTT00000012092 Transcript upstream_gene_variant - - - - - - DISTANCE=306 rs524522 12:57869500 C CCDS53807.1 CCDS53807.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3656 rs524522 12:57869500 C CCDS53806.1 CCDS53806.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3656 rs534578 12:57877330 C - ENSR00001463921 RegulatoryFeature regulatory_region_variant - - - - - - rs534578 12:57877330 C 64333 NM_001080157.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3906 rs534578 12:57877330 C CCDS8941.2 CCDS8941.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4141 rs534578 12:57877330 C 4141 NM_004990.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4406 rs534578 12:57877330 C ENSESTG00000004610 ENSESTT00000011756 Transcript upstream_gene_variant - - - - - - DISTANCE=4524 rs534578 12:57877330 C CCDS8942.1 CCDS8942.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4544 rs534578 12:57877330 C 64333 NM_032496.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3697 rs534578 12:57877330 C ENSESTG00000004610 ENSESTT00000011746 Transcript upstream_gene_variant - - - - - - DISTANCE=4521 rs534578 12:57877330 C CCDS44929.1 CCDS44929.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4141 rs534578 12:57877330 C ENSESTG00000004601 ENSESTT00000011600 Transcript intron_variant - - - - - - rs534578 12:57877330 C ENSESTG00000004610 ENSESTT00000011727 Transcript upstream_gene_variant - - - - - - DISTANCE=4521 rs2720189 12:58399657 G - - - intergenic_variant - - - - - - rs2720180 12:58481656 G - - - intergenic_variant - - - - - - rs905370 12:58591132 A - - - intergenic_variant - - - - - - rs981036 12:61149536 G - - - intergenic_variant - - - - - - rs4562895 12:61623094 C - - - intergenic_variant - - - - - - rs4758843 12:62071368 T - - - intergenic_variant - - - - - - rs11174165 12:62159021 G CCDS8962.1 CCDS8962.1 Transcript intron_variant - - - - - - rs11174165 12:62159021 G ENSESTG00000008462 ENSESTT00000021356 Transcript intron_variant - - - - - - rs11174165 12:62159021 G ENSESTG00000008462 ENSESTT00000021349 Transcript intron_variant - - - - - - rs11174165 12:62159021 G ENSESTG00000008462 ENSESTT00000021321 Transcript intron_variant - - - - - - rs11174165 12:62159021 G 338811 NM_178539.4 Transcript intron_variant - - - - - - rs11174165 12:62159021 G ENSESTG00000008462 ENSESTT00000021354 Transcript intron_variant - - - - - - rs11174165 12:62159021 G ENSESTG00000008462 ENSESTT00000021310 Transcript intron_variant - - - - - - rs11174165 12:62159021 G ENSESTG00000008462 ENSESTT00000021347 Transcript intron_variant - - - - - - rs11174165 12:62159021 G ENSESTG00000008462 ENSESTT00000021357 Transcript intron_variant - - - - - - rs11174165 12:62159021 G ENSESTG00000008462 ENSESTT00000021352 Transcript intron_variant - - - - - - rs11174165 12:62159021 G ENSESTG00000008462 ENSESTT00000021322 Transcript intron_variant - - - - - - rs2639729 12:62600012 A ENSESTG00000008418 ENSESTT00000021258 Transcript downstream_gene_variant - - - - - - DISTANCE=658 rs561106 12:62835080 G - - - intergenic_variant - - - - - - rs7953461 12:62939391 C 23041 NM_015026.2 Transcript intron_variant - - - - - - rs7953461 12:62939391 C ENSESTG00000031245 ENSESTT00000078819 Transcript upstream_gene_variant - - - - - - DISTANCE=1283 rs7953461 12:62939391 C CCDS31849.1 CCDS31849.1 Transcript intron_variant - - - - - - rs771975 12:63389013 C - ENSR00000431864 RegulatoryFeature regulatory_region_variant - - - - - - rs771975 12:63389013 C - - - intergenic_variant - - - - - - rs1250289 12:63465526 A - - - intergenic_variant - - - - - - rs542825 12:63808612 G - - - intergenic_variant - - - - - - rs789708 12:64466017 G ENSESTG00000029445 ENSESTT00000074436 Transcript intron_variant - - - - - - rs789708 12:64466017 G ENSESTG00000030078 ENSESTT00000075679 Transcript intron_variant - - - - - - rs789708 12:64466017 G CCDS8967.1 CCDS8967.1 Transcript intron_variant - - - - - - rs789708 12:64466017 G ENSESTG00000029445 ENSESTT00000074457 Transcript intron_variant - - - - - - rs789708 12:64466017 G ENSESTG00000029445 ENSESTT00000074446 Transcript intron_variant - - - - - - rs789708 12:64466017 G ENSESTG00000029445 ENSESTT00000074424 Transcript intron_variant - - - - - - rs789708 12:64466017 G 57522 NM_020762.2 Transcript intron_variant - - - - - - rs790009 12:64603949 C ENSESTG00000030051 ENSESTT00000075620 Transcript intron_variant - - - - - - rs790009 12:64603949 C CCDS41803.1 CCDS41803.1 Transcript intron_variant - - - - - - rs790009 12:64603949 C ENSESTG00000030051 ENSESTT00000075654 Transcript intron_variant - - - - - - rs790009 12:64603949 C 144577 NM_152440.4 Transcript intron_variant - - - - - - rs1797698 12:65040373 T ENSESTG00000005597 ENSESTT00000014241 Transcript intron_variant - - - - - - rs1797698 12:65040373 T 283349 NM_178169.3 Transcript intron_variant - - - - - - rs1797698 12:65040373 T CCDS8969.1 CCDS8969.1 Transcript intron_variant - - - - - - rs1797698 12:65040373 T 283349 NR_040718.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1147086 12:65259635 T CCDS53813.1 CCDS53813.1 Transcript intron_variant - - - - - - rs1147086 12:65259635 T ENSESTG00000005622 ENSESTT00000014277 Transcript intron_variant - - - - - - rs1147086 12:65259635 T 23329 NM_015279.1 Transcript intron_variant - - - - - - rs10878241 12:65588087 A CCDS8972.1 CCDS8972.1 Transcript intron_variant - - - - - - rs10878241 12:65588087 A 23592 NM_001167614.1 Transcript intron_variant - - - - - - rs10878241 12:65588087 A 23592 NM_014319.4 Transcript intron_variant - - - - - - rs9325179 12:65725167 C ENSESTG00000005656 ENSESTT00000014406 Transcript intron_variant - - - - - - rs9325179 12:65725167 C 253827 NM_001193461.1 Transcript intron_variant - - - - - - rs9325179 12:65725167 C 253827 NM_198080.3 Transcript intron_variant - - - - - - rs9325179 12:65725167 C 253827 NM_001031679.2 Transcript intron_variant - - - - - - rs9325179 12:65725167 C ENSESTG00000005656 ENSESTT00000014401 Transcript intron_variant - - - - - - rs9325179 12:65725167 C ENSESTG00000005656 ENSESTT00000014363 Transcript downstream_gene_variant - - - - - - DISTANCE=2780 rs9325179 12:65725167 C 253827 NM_001193460.1 Transcript intron_variant - - - - - - rs9325179 12:65725167 C ENSESTG00000005656 ENSESTT00000014394 Transcript intron_variant - - - - - - rs9325179 12:65725167 C CCDS31853.1 CCDS31853.1 Transcript intron_variant - - - - - - rs9325179 12:65725167 C CCDS8973.1 CCDS8973.1 Transcript intron_variant - - - - - - rs56290526 12:65897565 C ENSESTG00000005683 ENSESTT00000014431 Transcript intron_variant - - - - - - rs56290526 12:65897565 C ENSESTG00000005683 ENSESTT00000014441 Transcript intron_variant - - - - - - rs2264888 12:65937040 C ENSESTG00000005683 ENSESTT00000014431 Transcript intron_variant - - - - - - rs2264888 12:65937040 C ENSESTG00000005683 ENSESTT00000014441 Transcript intron_variant - - - - - - rs2464305 12:66513159 G CCDS8974.1 CCDS8974.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4461 rs2464305 12:66513159 G 84298 NM_032338.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3690 rs2464304 12:66517828 A CCDS8974.1 CCDS8974.1 Transcript intron_variant - - - - - - rs2464304 12:66517828 A 84298 NM_032338.3 Transcript intron_variant - - - - - - rs1168755 12:66531149 C 51643 NM_016056.2 Transcript 3_prime_UTR_variant 1384 - - - - - rs1168755 12:66531149 C ENSESTG00000012427 ENSESTT00000031172 Transcript downstream_gene_variant - - - - - - DISTANCE=559 rs1168755 12:66531149 C CCDS41805.1 CCDS41805.1 Transcript downstream_gene_variant - - - - - - DISTANCE=591 rs2464303 12:66540613 A 51643 NM_016056.2 Transcript intron_variant - - - - - - rs2464303 12:66540613 A ENSESTG00000012427 ENSESTT00000031172 Transcript intron_variant - - - - - - rs2464303 12:66540613 A CCDS41805.1 CCDS41805.1 Transcript intron_variant - - - - - - rs2464302 12:66576895 A - - - intergenic_variant - - - - - - rs4244066 12:67007908 G ENSESTG00000012380 ENSESTT00000031109 Transcript intron_variant - - - - - - rs4244066 12:67007908 G CCDS41807.1 CCDS41807.1 Transcript intron_variant - - - - - - rs4244066 12:67007908 G ENSESTG00000012380 ENSESTT00000031104 Transcript intron_variant - - - - - - rs4244066 12:67007908 G ENSESTG00000009440 ENSESTT00000023664 Transcript intron_variant - - - - - - rs4244066 12:67007908 G ENSESTG00000012380 ENSESTT00000031059 Transcript intron_variant - - - - - - rs4244066 12:67007908 G ENSESTG00000012380 ENSESTT00000031110 Transcript intron_variant - - - - - - rs4244066 12:67007908 G 23426 NM_001178074.1 Transcript intron_variant - - - - - - rs4244066 12:67007908 G 23426 NM_021150.3 Transcript intron_variant - - - - - - rs4244066 12:67007908 G ENSESTG00000009440 ENSESTT00000023661 Transcript intron_variant - - - - - - rs12299575 12:67032378 G ENSESTG00000012380 ENSESTT00000031109 Transcript intron_variant - - - - - - rs12299575 12:67032378 G CCDS41807.1 CCDS41807.1 Transcript intron_variant - - - - - - rs12299575 12:67032378 G ENSESTG00000012380 ENSESTT00000031104 Transcript intron_variant - - - - - - rs12299575 12:67032378 G ENSESTG00000012380 ENSESTT00000031059 Transcript intron_variant - - - - - - rs12299575 12:67032378 G ENSESTG00000012380 ENSESTT00000031110 Transcript intron_variant - - - - - - rs12299575 12:67032378 G 23426 NM_001178074.1 Transcript intron_variant - - - - - - rs12299575 12:67032378 G 23426 NM_021150.3 Transcript intron_variant - - - - - - rs12299575 12:67032378 G ENSESTG00000009440 ENSESTT00000023661 Transcript intron_variant - - - - - - rs1383105 12:67145909 G - - - intergenic_variant - - - - - - rs10735938 12:67167698 G - - - intergenic_variant - - - - - - rs1252261 12:67257952 A - - - intergenic_variant - - - - - - rs2049569 12:67482141 A - - - intergenic_variant - - - - - - rs7974734 12:68085802 T - - - intergenic_variant - - - - - - rs7313615 12:68304928 C - ENSR00001464534 RegulatoryFeature regulatory_region_variant - - - - - - rs7313615 12:68304928 C - - - intergenic_variant - - - - - - rs7312609 12:68676205 G - - - intergenic_variant - - - - - - rs10784706 12:68722254 G ENSESTG00000025735 ENSESTT00000064994 Transcript upstream_gene_variant - - - - - - DISTANCE=2364 rs10784706 12:68722254 G ENSESTG00000025735 ENSESTT00000064963 Transcript intron_variant - - - - - - rs10784706 12:68722254 G CCDS8983.1 CCDS8983.1 Transcript intron_variant - - - - - - rs10784706 12:68722254 G CCDS55841.1 CCDS55841.1 Transcript intron_variant - - - - - - rs10784706 12:68722254 G 56890 NM_017440.4 Transcript intron_variant - - - - - - rs10784706 12:68722254 G 56890 NM_001205029.1 Transcript intron_variant - - - - - - rs10784706 12:68722254 G CCDS44938.1 CCDS44938.1 Transcript intron_variant - - - - - - rs10784706 12:68722254 G 56890 NM_020128.2 Transcript intron_variant - - - - - - rs10784706 12:68722254 G ENSESTG00000025719 ENSESTT00000064848 Transcript downstream_gene_variant - - - - - - DISTANCE=4474 rs10784706 12:68722254 G ENSESTG00000025735 ENSESTT00000064962 Transcript intron_variant - - - - - - rs10784706 12:68722254 G 56890 NM_001205028.1 Transcript intron_variant - - - - - - rs10784706 12:68722254 G ENSESTG00000025735 ENSESTT00000064937 Transcript intron_variant - - - - - - rs10784706 12:68722254 G ENSESTG00000025735 ENSESTT00000064902 Transcript intron_variant - - - - - - rs10784706 12:68722254 G CCDS55842.1 CCDS55842.1 Transcript intron_variant - - - - - - rs4913444 12:68795510 G ENSESTG00000025719 ENSESTT00000064848 Transcript intron_variant - - - - - - rs7316589 12:68824792 A - - - intergenic_variant - - - - - - rs7969418 12:69624955 C - - - intergenic_variant - - - - - - rs317671 12:69699670 G - - - intergenic_variant - - - - - - rs2951681 12:70267460 A - ENSR00000432713 RegulatoryFeature regulatory_region_variant - - - - - - rs2951681 12:70267460 A - - - intergenic_variant - - - - - - rs1022243 12:71199537 G CCDS8998.1 CCDS8998.1 Transcript intron_variant - - - - - - rs1022243 12:71199537 G 5801 NM_002849.3 Transcript intron_variant - - - - - - rs6582030 12:71802408 G - - - intergenic_variant - - - - - - rs4350442 12:71844550 A CCDS9000.1 CCDS9000.1 Transcript intron_variant - - - - - - rs4350442 12:71844550 A 8549 NM_003667.2 Transcript intron_variant - - - - - - rs4350442 12:71844550 A ENSESTG00000002028 ENSESTT00000005050 Transcript intron_variant - - - - - - rs6582047 12:72064379 A ENSESTG00000030858 ENSESTT00000077817 Transcript intron_variant - - - - - - rs6582047 12:72064379 A ENSESTG00000030858 ENSESTT00000077786 Transcript intron_variant - - - - - - rs6582047 12:72064379 A ENSESTG00000031584 ENSESTT00000079723 Transcript upstream_gene_variant - - - - - - DISTANCE=2874 rs6582047 12:72064379 A 83591 NM_031435.3 Transcript intron_variant - - - - - - rs6582047 12:72064379 A ENSESTG00000030858 ENSESTT00000077772 Transcript intron_variant - - - - - - rs6582047 12:72064379 A CCDS9001.1 CCDS9001.1 Transcript intron_variant - - - - - - rs6582047 12:72064379 A ENSESTG00000031584 ENSESTT00000079710 Transcript upstream_gene_variant - - - - - - DISTANCE=2874 rs6582047 12:72064379 A ENSESTG00000030858 ENSESTT00000077833 Transcript intron_variant - - - - - - rs6582047 12:72064379 A ENSESTG00000030858 ENSESTT00000077802 Transcript intron_variant - - - - - - rs1403307 12:72508984 C - - - intergenic_variant - - - - - - rs2730667 12:72615106 C - - - intergenic_variant - - - - - - rs1348575 12:72754310 C CCDS9004.1 CCDS9004.1 Transcript intron_variant - - - - - - rs1348575 12:72754310 C 29953 NM_013381.2 Transcript intron_variant - - - - - - rs1444605 12:72824511 T CCDS9004.1 CCDS9004.1 Transcript intron_variant - - - - - - rs1444605 12:72824511 T ENSESTG00000031542 ENSESTT00000079583 Transcript intron_variant - - - - - - rs1444605 12:72824511 T 29953 NM_013381.2 Transcript intron_variant - - - - - - rs7968497 12:73244106 C - - - intergenic_variant - - - - - - rs1516271 12:73419439 T - - - intergenic_variant - - - - - - rs2586907 12:73956578 C - - - intergenic_variant - - - - - - rs1609027 12:75409494 A - - - intergenic_variant - - - - - - rs4882672 12:75447172 T CCDS9007.1 CCDS9007.1 Transcript intron_variant - - - - - - rs4882672 12:75447172 T CCDS58256.1 CCDS58256.1 Transcript intron_variant - - - - - - rs4882672 12:75447172 T 3747 NM_153748.2 Transcript intron_variant - - - - - - rs4882672 12:75447172 T CCDS9005.1 CCDS9005.1 Transcript intron_variant - - - - - - rs4882672 12:75447172 T 3747 NM_001260499.1 Transcript intron_variant - - - - - - rs4882672 12:75447172 T 3747 NM_139137.3 Transcript intron_variant - - - - - - rs4882672 12:75447172 T 3747 NM_001260498.1 Transcript intron_variant - - - - - - rs4882672 12:75447172 T CCDS9006.1 CCDS9006.1 Transcript intron_variant - - - - - - rs4882672 12:75447172 T ENSESTG00000020135 ENSESTT00000050473 Transcript upstream_gene_variant - - - - - - DISTANCE=2523 rs4882672 12:75447172 T CCDS58255.1 CCDS58255.1 Transcript intron_variant - - - - - - rs4882672 12:75447172 T CCDS58257.1 CCDS58257.1 Transcript intron_variant - - - - - - rs4882672 12:75447172 T 3747 NM_139136.3 Transcript intron_variant - - - - - - rs4882672 12:75447172 T ENSESTG00000020129 ENSESTT00000050455 Transcript intron_variant - - - - - - rs4882672 12:75447172 T 3747 NM_001260497.1 Transcript intron_variant - - - - - - rs2960464 12:75534240 T CCDS9007.1 CCDS9007.1 Transcript intron_variant - - - - - - rs2960464 12:75534240 T CCDS58256.1 CCDS58256.1 Transcript intron_variant - - - - - - rs2960464 12:75534240 T 3747 NM_153748.2 Transcript intron_variant - - - - - - rs2960464 12:75534240 T CCDS9005.1 CCDS9005.1 Transcript intron_variant - - - - - - rs2960464 12:75534240 T 3747 NM_001260499.1 Transcript intron_variant - - - - - - rs2960464 12:75534240 T 3747 NM_139137.3 Transcript intron_variant - - - - - - rs2960464 12:75534240 T 3747 NM_001260498.1 Transcript intron_variant - - - - - - rs2960464 12:75534240 T CCDS9006.1 CCDS9006.1 Transcript intron_variant - - - - - - rs2960464 12:75534240 T CCDS58255.1 CCDS58255.1 Transcript intron_variant - - - - - - rs2960464 12:75534240 T CCDS58257.1 CCDS58257.1 Transcript intron_variant - - - - - - rs2960464 12:75534240 T 3747 NM_139136.3 Transcript intron_variant - - - - - - rs2960464 12:75534240 T ENSESTG00000020129 ENSESTT00000050455 Transcript intron_variant - - - - - - rs2960464 12:75534240 T 3747 NM_001260497.1 Transcript intron_variant - - - - - - rs2926145 12:75562536 A CCDS9007.1 CCDS9007.1 Transcript intron_variant - - - - - - rs2926145 12:75562536 A CCDS58256.1 CCDS58256.1 Transcript intron_variant - - - - - - rs2926145 12:75562536 A 3747 NM_153748.2 Transcript intron_variant - - - - - - rs2926145 12:75562536 A CCDS9005.1 CCDS9005.1 Transcript intron_variant - - - - - - rs2926145 12:75562536 A 3747 NM_001260499.1 Transcript intron_variant - - - - - - rs2926145 12:75562536 A 3747 NM_139137.3 Transcript intron_variant - - - - - - rs2926145 12:75562536 A 3747 NM_001260498.1 Transcript intron_variant - - - - - - rs2926145 12:75562536 A CCDS9006.1 CCDS9006.1 Transcript intron_variant - - - - - - rs2926145 12:75562536 A CCDS58255.1 CCDS58255.1 Transcript intron_variant - - - - - - rs2926145 12:75562536 A CCDS58257.1 CCDS58257.1 Transcript intron_variant - - - - - - rs2926145 12:75562536 A 3747 NM_139136.3 Transcript intron_variant - - - - - - rs2926145 12:75562536 A ENSESTG00000020129 ENSESTT00000050455 Transcript intron_variant - - - - - - rs2926145 12:75562536 A 3747 NM_001260497.1 Transcript intron_variant - - - - - - rs2960465 12:75565616 T CCDS9007.1 CCDS9007.1 Transcript intron_variant - - - - - - rs2960465 12:75565616 T CCDS58256.1 CCDS58256.1 Transcript intron_variant - - - - - - rs2960465 12:75565616 T 3747 NM_153748.2 Transcript intron_variant - - - - - - rs2960465 12:75565616 T CCDS9005.1 CCDS9005.1 Transcript intron_variant - - - - - - rs2960465 12:75565616 T 3747 NM_001260499.1 Transcript intron_variant - - - - - - rs2960465 12:75565616 T 3747 NM_139137.3 Transcript intron_variant - - - - - - rs2960465 12:75565616 T 3747 NM_001260498.1 Transcript intron_variant - - - - - - rs2960465 12:75565616 T CCDS9006.1 CCDS9006.1 Transcript intron_variant - - - - - - rs2960465 12:75565616 T CCDS58255.1 CCDS58255.1 Transcript intron_variant - - - - - - rs2960465 12:75565616 T CCDS58257.1 CCDS58257.1 Transcript intron_variant - - - - - - rs2960465 12:75565616 T 3747 NM_139136.3 Transcript intron_variant - - - - - - rs2960465 12:75565616 T ENSESTG00000020129 ENSESTT00000050455 Transcript intron_variant - - - - - - rs2960465 12:75565616 T 3747 NM_001260497.1 Transcript intron_variant - - - - - - rs2960466 12:75574781 T CCDS9007.1 CCDS9007.1 Transcript intron_variant - - - - - - rs2960466 12:75574781 T CCDS58256.1 CCDS58256.1 Transcript intron_variant - - - - - - rs2960466 12:75574781 T 3747 NM_153748.2 Transcript intron_variant - - - - - - rs2960466 12:75574781 T CCDS9005.1 CCDS9005.1 Transcript intron_variant - - - - - - rs2960466 12:75574781 T 3747 NM_001260499.1 Transcript intron_variant - - - - - - rs2960466 12:75574781 T 3747 NM_139137.3 Transcript intron_variant - - - - - - rs2960466 12:75574781 T 3747 NM_001260498.1 Transcript intron_variant - - - - - - rs2960466 12:75574781 T CCDS9006.1 CCDS9006.1 Transcript intron_variant - - - - - - rs2960466 12:75574781 T CCDS58255.1 CCDS58255.1 Transcript intron_variant - - - - - - rs2960466 12:75574781 T CCDS58257.1 CCDS58257.1 Transcript intron_variant - - - - - - rs2960466 12:75574781 T 3747 NM_139136.3 Transcript intron_variant - - - - - - rs2960466 12:75574781 T ENSESTG00000020129 ENSESTT00000050455 Transcript intron_variant - - - - - - rs2960466 12:75574781 T 3747 NM_001260497.1 Transcript intron_variant - - - - - - rs2960467 12:75574787 C CCDS9007.1 CCDS9007.1 Transcript intron_variant - - - - - - rs2960467 12:75574787 C CCDS58256.1 CCDS58256.1 Transcript intron_variant - - - - - - rs2960467 12:75574787 C 3747 NM_153748.2 Transcript intron_variant - - - - - - rs2960467 12:75574787 C CCDS9005.1 CCDS9005.1 Transcript intron_variant - - - - - - rs2960467 12:75574787 C 3747 NM_001260499.1 Transcript intron_variant - - - - - - rs2960467 12:75574787 C 3747 NM_139137.3 Transcript intron_variant - - - - - - rs2960467 12:75574787 C 3747 NM_001260498.1 Transcript intron_variant - - - - - - rs2960467 12:75574787 C CCDS9006.1 CCDS9006.1 Transcript intron_variant - - - - - - rs2960467 12:75574787 C CCDS58255.1 CCDS58255.1 Transcript intron_variant - - - - - - rs2960467 12:75574787 C CCDS58257.1 CCDS58257.1 Transcript intron_variant - - - - - - rs2960467 12:75574787 C 3747 NM_139136.3 Transcript intron_variant - - - - - - rs2960467 12:75574787 C ENSESTG00000020129 ENSESTT00000050455 Transcript intron_variant - - - - - - rs2960467 12:75574787 C 3747 NM_001260497.1 Transcript intron_variant - - - - - - rs2960468 12:75574935 G CCDS9007.1 CCDS9007.1 Transcript intron_variant - - - - - - rs2960468 12:75574935 G CCDS58256.1 CCDS58256.1 Transcript intron_variant - - - - - - rs2960468 12:75574935 G 3747 NM_153748.2 Transcript intron_variant - - - - - - rs2960468 12:75574935 G CCDS9005.1 CCDS9005.1 Transcript intron_variant - - - - - - rs2960468 12:75574935 G 3747 NM_001260499.1 Transcript intron_variant - - - - - - rs2960468 12:75574935 G 3747 NM_139137.3 Transcript intron_variant - - - - - - rs2960468 12:75574935 G 3747 NM_001260498.1 Transcript intron_variant - - - - - - rs2960468 12:75574935 G CCDS9006.1 CCDS9006.1 Transcript intron_variant - - - - - - rs2960468 12:75574935 G CCDS58255.1 CCDS58255.1 Transcript intron_variant - - - - - - rs2960468 12:75574935 G CCDS58257.1 CCDS58257.1 Transcript intron_variant - - - - - - rs2960468 12:75574935 G 3747 NM_139136.3 Transcript intron_variant - - - - - - rs2960468 12:75574935 G ENSESTG00000020129 ENSESTT00000050455 Transcript intron_variant - - - - - - rs2960468 12:75574935 G 3747 NM_001260497.1 Transcript intron_variant - - - - - - rs2446340 12:75580517 C CCDS9007.1 CCDS9007.1 Transcript intron_variant - - - - - - rs2446340 12:75580517 C CCDS58256.1 CCDS58256.1 Transcript intron_variant - - - - - - rs2446340 12:75580517 C 3747 NM_153748.2 Transcript intron_variant - - - - - - rs2446340 12:75580517 C CCDS9005.1 CCDS9005.1 Transcript intron_variant - - - - - - rs2446340 12:75580517 C 3747 NM_001260499.1 Transcript intron_variant - - - - - - rs2446340 12:75580517 C 3747 NM_139137.3 Transcript intron_variant - - - - - - rs2446340 12:75580517 C 3747 NM_001260498.1 Transcript intron_variant - - - - - - rs2446340 12:75580517 C CCDS9006.1 CCDS9006.1 Transcript intron_variant - - - - - - rs2446340 12:75580517 C CCDS58255.1 CCDS58255.1 Transcript intron_variant - - - - - - rs2446340 12:75580517 C CCDS58257.1 CCDS58257.1 Transcript intron_variant - - - - - - rs2446340 12:75580517 C 3747 NM_139136.3 Transcript intron_variant - - - - - - rs2446340 12:75580517 C ENSESTG00000020129 ENSESTT00000050455 Transcript intron_variant - - - - - - rs2446340 12:75580517 C 3747 NM_001260497.1 Transcript intron_variant - - - - - - rs2960462 12:75608931 C - - - intergenic_variant - - - - - - rs7972989 12:75704477 C ENSESTG00000020039 ENSESTT00000050252 Transcript intron_variant - - - - - - rs7972989 12:75704477 C 84698 NM_032606.3 Transcript intron_variant - - - - - - rs7972989 12:75704477 C ENSESTG00000020039 ENSESTT00000050284 Transcript intron_variant - - - - - - rs7972989 12:75704477 C CCDS9008.2 CCDS9008.2 Transcript intron_variant - - - - - - rs7972989 12:75704477 C ENSESTG00000020039 ENSESTT00000050353 Transcript intron_variant - - - - - - rs7972989 12:75704477 C ENSESTG00000020039 ENSESTT00000050280 Transcript intron_variant - - - - - - rs1275704 12:75934296 C - - - intergenic_variant - - - - - - rs7488392 12:76093872 C - ENSR00000433112 RegulatoryFeature regulatory_region_variant - - - - - - rs7488392 12:76093872 C - - - intergenic_variant - - - - - - rs2367445 12:76398762 T - - - intergenic_variant - - - - - - rs7136020 12:76758836 G CCDS41814.1 CCDS41814.1 Transcript intron_variant - - - - - - rs7136020 12:76758836 G CCDS31862.1 CCDS31862.1 Transcript intron_variant - - - - - - rs7136020 12:76758836 G 114882 NM_001003712.1 Transcript intron_variant - - - - - - rs7136020 12:76758836 G 114882 NM_020841.4 Transcript intron_variant - - - - - - rs941176 12:77754463 G - - - intergenic_variant - - - - - - rs711118 12:78014136 C - - - intergenic_variant - - - - - - rs1241965 12:78550783 A - ENSR00000433408 RegulatoryFeature regulatory_region_variant - - - - - - rs1241965 12:78550783 A 89795 NM_014903.4 Transcript intron_variant - - - - - - rs1241965 12:78550783 A ENSESTG00000021564 ENSESTT00000054328 Transcript intron_variant - - - - - - rs1241965 12:78550783 A CCDS41815.1 CCDS41815.1 Transcript intron_variant - - - - - - rs2463174 12:78603553 T ENSESTG00000021564 ENSESTT00000054531 Transcript intron_variant - - - - - - rs2463174 12:78603553 T 89795 NM_014903.4 Transcript intron_variant - - - - - - rs2463174 12:78603553 T ENSESTG00000021564 ENSESTT00000054328 Transcript intron_variant - - - - - - rs2463174 12:78603553 T ENSESTG00000021564 ENSESTT00000054481 Transcript intron_variant - - - - - - rs2463174 12:78603553 T ENSESTG00000021564 ENSESTT00000054525 Transcript intron_variant - - - - - - rs2463174 12:78603553 T ENSESTG00000021564 ENSESTT00000054517 Transcript intron_variant - - - - - - rs2463174 12:78603553 T ENSESTG00000021748 ENSESTT00000054605 Transcript downstream_gene_variant - - - - - - DISTANCE=1610 rs2463174 12:78603553 T ENSESTG00000021564 ENSESTT00000054511 Transcript intron_variant - - - - - - rs2463174 12:78603553 T CCDS41815.1 CCDS41815.1 Transcript intron_variant - - - - - - rs300453 12:78610504 T ENSESTG00000021748 ENSESTT00000054605 Transcript upstream_gene_variant - - - - - - DISTANCE=4713 rs300453 12:78610504 T 89795 NM_014903.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3714 rs516336 12:78759843 C - - - intergenic_variant - - - - - - rs1717393 12:78949262 G - - - intergenic_variant - - - - - - rs1717359 12:78986641 C - - - intergenic_variant - - - - - - rs1795990 12:78989855 G - - - intergenic_variant - - - - - - rs941137 12:79647065 A 6857 NM_005639.2 Transcript intron_variant - - - - - - rs941137 12:79647065 A ENSESTG00000012600 ENSESTT00000031592 Transcript intron_variant - - - - - - rs941137 12:79647065 A 6857 NM_001135806.1 Transcript intron_variant - - - - - - rs941137 12:79647065 A CCDS9017.1 CCDS9017.1 Transcript intron_variant - - - - - - rs941137 12:79647065 A ENSESTG00000012567 ENSESTT00000031568 Transcript intron_variant - - - - - - rs941137 12:79647065 A ENSESTG00000012567 ENSESTT00000031570 Transcript intron_variant - - - - - - rs941137 12:79647065 A ENSESTG00000012567 ENSESTT00000031541 Transcript intron_variant - - - - - - rs941137 12:79647065 A 6857 NM_001135805.1 Transcript intron_variant - - - - - - rs4240715 12:79884445 C ENSESTG00000012594 ENSESTT00000031579 Transcript intron_variant - - - - - - rs2656033 12:80252265 G CCDS58260.1 CCDS58260.1 Transcript intron_variant - - - - - - rs2656033 12:80252265 G 4659 NM_001143885.1 Transcript intron_variant - - - - - - rs2656033 12:80252265 G 4659 NM_001244992.1 Transcript intron_variant - - - - - - rs2656033 12:80252265 G 4659 NM_001143886.1 Transcript intron_variant - - - - - - rs2656033 12:80252265 G CCDS44948.1 CCDS44948.1 Transcript intron_variant - - - - - - rs2656033 12:80252265 G CCDS44947.1 CCDS44947.1 Transcript intron_variant - - - - - - rs2656033 12:80252265 G 4659 NM_001244990.1 Transcript intron_variant - - - - - - rs2656033 12:80252265 G ENSESTG00000001568 ENSESTT00000003773 Transcript intron_variant - - - - - - rs2656033 12:80252265 G ENSESTG00000001568 ENSESTT00000003770 Transcript intron_variant - - - - - - rs2656033 12:80252265 G 4659 NM_002480.2 Transcript intron_variant - - - - - - rs2656033 12:80252265 G CCDS58259.1 CCDS58259.1 Transcript intron_variant - - - - - - rs4313640 12:80830638 T ENSESTG00000001542 ENSESTT00000003646 Transcript intron_variant - - - - - - rs4313640 12:80830638 T ENSESTG00000001542 ENSESTT00000003642 Transcript intron_variant - - - - - - rs4313640 12:80830638 T ENSESTG00000001542 ENSESTT00000003649 Transcript intron_variant - - - - - - rs4313640 12:80830638 T ENSESTG00000001542 ENSESTT00000003650 Transcript intron_variant - - - - - - rs4842362 12:81236511 A ENSESTG00000005785 ENSESTT00000014652 Transcript intron_variant - - - - - - rs4842362 12:81236511 A ENSESTG00000005785 ENSESTT00000014641 Transcript intron_variant - - - - - - rs4842362 12:81236511 A 8825 NM_004664.2 Transcript intron_variant - - - - - - rs4842362 12:81236511 A CCDS9021.1 CCDS9021.1 Transcript intron_variant - - - - - - rs4842363 12:81236575 C ENSESTG00000005785 ENSESTT00000014652 Transcript intron_variant - - - - - - rs4842363 12:81236575 C ENSESTG00000005785 ENSESTT00000014641 Transcript intron_variant - - - - - - rs4842363 12:81236575 C 8825 NM_004664.2 Transcript intron_variant - - - - - - rs4842363 12:81236575 C CCDS9021.1 CCDS9021.1 Transcript intron_variant - - - - - - rs10862328 12:82005497 C CCDS55854.1 CCDS55854.1 Transcript intron_variant - - - - - - rs10862328 12:82005497 C CCDS55857.1 CCDS55857.1 Transcript intron_variant - - - - - - rs10862328 12:82005497 C 8499 NM_001220476.1 Transcript intron_variant - - - - - - rs10862328 12:82005497 C CCDS55855.1 CCDS55855.1 Transcript intron_variant - - - - - - rs10862328 12:82005497 C 8499 NM_001220473.1 Transcript intron_variant - - - - - - rs10862328 12:82005497 C 8499 NM_003625.3 Transcript intron_variant - - - - - - rs10862328 12:82005497 C 8499 NM_001220474.1 Transcript intron_variant - - - - - - rs10862328 12:82005497 C 8499 NM_001220475.1 Transcript intron_variant - - - - - - rs10862328 12:82005497 C CCDS55856.1 CCDS55856.1 Transcript intron_variant - - - - - - rs1922547 12:82168132 C - - - intergenic_variant - - - - - - rs7965798 12:82318100 A - - - intergenic_variant - - - - - - rs4556625 12:82589512 A - - - intergenic_variant - - - - - - rs2717451 12:82825581 C ENSESTG00000019999 ENSESTT00000050117 Transcript intron_variant - - - - - - rs2717451 12:82825581 C 84190 NM_032230.2 Transcript intron_variant - - - - - - rs2717451 12:82825581 C CCDS9024.1 CCDS9024.1 Transcript intron_variant - - - - - - rs2642013 12:82833475 G ENSESTG00000019999 ENSESTT00000050117 Transcript downstream_gene_variant - - - - - - DISTANCE=610 rs2642013 12:82833475 G 84190 NM_032230.2 Transcript intron_variant - - - - - - rs2642013 12:82833475 G CCDS9024.1 CCDS9024.1 Transcript intron_variant - - - - - - rs2717447 12:82835268 A ENSESTG00000019999 ENSESTT00000050117 Transcript downstream_gene_variant - - - - - - DISTANCE=2403 rs2717447 12:82835268 A 84190 NM_032230.2 Transcript intron_variant - - - - - - rs2717447 12:82835268 A CCDS9024.1 CCDS9024.1 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061424 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061393 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061374 Transcript intron_variant - - - - - - rs7961012 12:83253590 G 160335 NM_152588.1 Transcript intron_variant - - - - - - rs7961012 12:83253590 G CCDS9025.1 CCDS9025.1 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061420 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061389 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061217 Transcript downstream_gene_variant - - - - - - DISTANCE=2569 rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061428 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061354 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061437 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061200 Transcript downstream_gene_variant - - - - - - DISTANCE=2634 rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061433 Transcript intron_variant - - - - - - rs7961012 12:83253590 G ENSESTG00000024219 ENSESTT00000061411 Transcript intron_variant - - - - - - rs3015647 12:85176864 T - - - intergenic_variant - - - - - - rs4376947 12:85241358 A - - - intergenic_variant - - - - - - rs4271424 12:85256370 T CCDS9026.1 CCDS9026.1 Transcript intron_variant - - - - - - rs4271424 12:85256370 T CCDS53816.1 CCDS53816.1 Transcript intron_variant - - - - - - rs4271424 12:85256370 T 55117 NM_001146335.2 Transcript intron_variant - - - - - - rs4271424 12:85256370 T 55117 NM_182767.5 Transcript intron_variant - - - - - - rs7314786 12:85268292 G - ENSR00000433897 RegulatoryFeature regulatory_region_variant - - - - - - rs7314786 12:85268292 G CCDS9026.1 CCDS9026.1 Transcript intron_variant - - - - - - rs7314786 12:85268292 G CCDS53816.1 CCDS53816.1 Transcript intron_variant - - - - - - rs7314786 12:85268292 G 55117 NM_001146335.2 Transcript intron_variant - - - - - - rs7314786 12:85268292 G 55117 NM_182767.5 Transcript intron_variant - - - - - - rs2949797 12:85269763 G CCDS9026.1 CCDS9026.1 Transcript intron_variant - - - - - - rs2949797 12:85269763 G CCDS53816.1 CCDS53816.1 Transcript intron_variant - - - - - - rs2949797 12:85269763 G 55117 NM_018057.6 Transcript downstream_gene_variant - - - - - - DISTANCE=4864 rs2949797 12:85269763 G 55117 NM_001146335.2 Transcript intron_variant - - - - - - rs2949797 12:85269763 G 55117 NM_182767.5 Transcript intron_variant - - - - - - rs2949799 12:85269965 T CCDS9026.1 CCDS9026.1 Transcript intron_variant - - - - - - rs2949799 12:85269965 T CCDS53816.1 CCDS53816.1 Transcript intron_variant - - - - - - rs2949799 12:85269965 T 55117 NM_018057.6 Transcript downstream_gene_variant - - - - - - DISTANCE=4662 rs2949799 12:85269965 T 55117 NM_001146335.2 Transcript intron_variant - - - - - - rs2949799 12:85269965 T 55117 NM_182767.5 Transcript intron_variant - - - - - - rs2949801 12:85302285 T ENSESTG00000017380 ENSESTT00000043763 Transcript intron_variant - - - - - - rs2949801 12:85302285 T 55117 NM_018057.6 Transcript intron_variant - - - - - - rs2949801 12:85302285 T ENSESTG00000017380 ENSESTT00000043785 Transcript intron_variant - - - - - - rs2949801 12:85302285 T 55117 NM_001146335.2 Transcript intron_variant - - - - - - rs2949801 12:85302285 T 55117 NM_182767.5 Transcript intron_variant - - - - - - rs7398753 12:85374265 T - - - intergenic_variant - - - - - - rs7132267 12:85418780 G 144448 NM_001100917.1 Transcript intron_variant - - - - - - rs7132267 12:85418780 G CCDS44949.1 CCDS44949.1 Transcript intron_variant - - - - - - rs10862952 12:85418827 G 144448 NM_001100917.1 Transcript intron_variant - - - - - - rs10862952 12:85418827 G CCDS44949.1 CCDS44949.1 Transcript intron_variant - - - - - - rs10746337 12:85443977 G ENSESTG00000017309 ENSESTT00000043570 Transcript upstream_gene_variant - - - - - - DISTANCE=2023 rs10746337 12:85443977 G ENSESTG00000017309 ENSESTT00000043559 Transcript intron_variant - - - - - - rs10746337 12:85443977 G ENSESTG00000017309 ENSESTT00000043548 Transcript intron_variant - - - - - - rs10746337 12:85443977 G CCDS41816.1 CCDS41816.1 Transcript intron_variant - - - - - - rs10746337 12:85443977 G 84125 NM_001079910.1 Transcript intron_variant - - - - - - rs7301495 12:85962623 G - - - intergenic_variant - - - - - - rs1374997 12:86363983 C - - - intergenic_variant - - - - - - rs2897239 12:86834808 C 25834 NM_013244.3 Transcript intron_variant - - - - - - rs7975144 12:87621151 T - ENSR00000089832 RegulatoryFeature regulatory_region_variant - - - - - - rs7975144 12:87621151 T - - - intergenic_variant - - - - - - rs6538066 12:87646239 C - - - intergenic_variant - - - - - - rs10777052 12:87870880 T - - - intergenic_variant - - - - - - rs2574886 12:88191508 A ENSESTG00000006121 ENSESTT00000015434 Transcript intron_variant - - - - - - rs990399 12:88264610 G - - - intergenic_variant - - - - - - rs1903447 12:88276662 G - - - intergenic_variant - - - - - - rs7960948 12:88295634 C - - - intergenic_variant - - - - - - rs4497486 12:88328124 T - - - intergenic_variant - - - - - - rs4620799 12:88350809 G - - - intergenic_variant - - - - - - rs4334111 12:88355871 A - - - intergenic_variant - - - - - - rs4842595 12:88415958 T 160419 NM_152589.1 Transcript intron_variant - - - - - - rs4842595 12:88415958 T ENSESTG00000006211 ENSESTT00000015666 Transcript intron_variant - - - - - - rs4842595 12:88415958 T ENSESTG00000006211 ENSESTT00000015669 Transcript intron_variant - - - - - - rs4842595 12:88415958 T ENSESTG00000006211 ENSESTT00000015660 Transcript intron_variant - - - - - - rs4842595 12:88415958 T CCDS9031.1 CCDS9031.1 Transcript intron_variant - - - - - - rs2468230 12:88547277 C ENSESTG00000006150 ENSESTT00000015499 Transcript synonymous_variant 608 399 133 H caT/caC - rs2468230 12:88547277 C CCDS9032.1 CCDS9032.1 Transcript synonymous_variant 399 399 133 H caT/caC - rs2468230 12:88547277 C 160418 NM_181783.3 Transcript synonymous_variant 619 399 133 H caT/caC - rs2468230 12:88547277 C ENSESTG00000006150 ENSESTT00000015500 Transcript intron_variant - - - - - - rs7488121 12:88604853 G - - - intergenic_variant - - - - - - rs10745473 12:88608343 T - - - intergenic_variant - - - - - - rs7307388 12:88657449 C - - - intergenic_variant - - - - - - rs10777104 12:88734031 G - ENSR00001465569 RegulatoryFeature regulatory_region_variant - - - - - - rs10777104 12:88734031 G - - - intergenic_variant - - - - - - rs4262787 12:88905251 G CCDS31867.1 CCDS31867.1 Transcript intron_variant - - - - - - rs4262787 12:88905251 G 4254 NM_003994.5 Transcript intron_variant - - - - - - rs4262787 12:88905251 G CCDS31868.1 CCDS31868.1 Transcript intron_variant - - - - - - rs4262787 12:88905251 G ENSESTG00000006161 ENSESTT00000015534 Transcript intron_variant - - - - - - rs4262787 12:88905251 G 4254 NM_000899.4 Transcript intron_variant - - - - - - rs4262787 12:88905251 G ENSESTG00000015482 ENSESTT00000038769 Transcript downstream_gene_variant - - - - - - DISTANCE=4918 rs198637 12:89316671 T - ENSR00001465610 RegulatoryFeature regulatory_region_variant - - - - - - rs198637 12:89316671 T - - - intergenic_variant - - - - - - rs4589356 12:89913556 T 100528030 NM_001199782.1 Transcript 3_prime_UTR_variant 4362 - - - - - rs4589356 12:89913556 T 282809 NM_172240.2 Transcript intron_variant - - - - - - rs4589356 12:89913556 T CCDS31869.1 CCDS31869.1 Transcript intron_variant - - - - - - rs4589356 12:89913556 T 282809 NR_037660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4589356 12:89913556 T 282809 NR_037659.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4589356 12:89913556 T ENSESTG00000015448 ENSESTT00000038724 Transcript intron_variant - - - - - - rs4589356 12:89913556 T ENSESTG00000015448 ENSESTT00000038712 Transcript intron_variant - - - - - - rs4589356 12:89913556 T ENSESTG00000015448 ENSESTT00000038679 Transcript intron_variant - - - - - - rs4589356 12:89913556 T CCDS55860.1 CCDS55860.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3034 rs4589356 12:89913556 T 100528030 NM_001199781.1 Transcript 3_prime_UTR_variant 5129 - - - - - rs4589356 12:89913556 T ENSESTG00000015448 ENSESTT00000038718 Transcript intron_variant - - - - - - rs4589356 12:89913556 T CCDS53817.1 CCDS53817.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3034 rs4589356 12:89913556 T CCDS55861.1 CCDS55861.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3034 rs4589356 12:89913556 T 8693 NM_003774.4 Transcript 3_prime_UTR_variant 5028 - - - - - rs4589356 12:89913556 T 282809 NM_001199777.1 Transcript intron_variant - - - - - - rs7980679 12:90032592 C ENSESTG00000005779 ENSESTT00000014684 Transcript downstream_gene_variant - - - - - - DISTANCE=3008 rs7980679 12:90032592 C 490 NM_001682.2 Transcript intron_variant - - - - - - rs7980679 12:90032592 C ENSESTG00000005779 ENSESTT00000014695 Transcript downstream_gene_variant - - - - - - DISTANCE=3008 rs7980679 12:90032592 C CCDS41817.1 CCDS41817.1 Transcript intron_variant - - - - - - rs7980679 12:90032592 C ENSESTG00000005779 ENSESTT00000014716 Transcript intron_variant - - - - - - rs7980679 12:90032592 C 490 NM_001001323.1 Transcript intron_variant - - - - - - rs7980679 12:90032592 C ENSESTG00000005779 ENSESTT00000014672 Transcript intron_variant - - - - - - rs7980679 12:90032592 C CCDS9035.1 CCDS9035.1 Transcript intron_variant - - - - - - rs4842683 12:90143142 C ENSESTG00000005779 ENSESTT00000014672 Transcript intron_variant - - - - - - rs4842694 12:90321227 A - ENSR00000434405 RegulatoryFeature regulatory_region_variant - - - - - - rs4842694 12:90321227 A ENSESTG00000005733 ENSESTT00000014520 Transcript intron_variant - - - - - - rs4842694 12:90321227 A ENSESTG00000005733 ENSESTT00000014523 Transcript intron_variant - - - - - - rs1231905 12:90678768 A - - - intergenic_variant - - - - - - rs10431403 12:91079197 C - - - intergenic_variant - - - - - - rs543931 12:91588067 A - - - intergenic_variant - - - - - - rs826754 12:91663995 T - - - intergenic_variant - - - - - - rs1493777 12:92171737 A - ENSR00001465847 RegulatoryFeature regulatory_region_variant - - - - - - rs1493777 12:92171737 A - - - intergenic_variant - - - - - - rs7980203 12:92886238 T - ENSR00001465909 RegulatoryFeature regulatory_region_variant - - - - - - rs7980203 12:92886238 T - - - intergenic_variant - - - - - - rs1872210 12:92984102 C - - - intergenic_variant - - - - - - rs10732652 12:93202079 T CCDS31874.1 CCDS31874.1 Transcript intron_variant - - - - - - rs10732652 12:93202079 T 8411 NM_003566.3 Transcript intron_variant - - - - - - rs6538359 12:93219282 T CCDS31874.1 CCDS31874.1 Transcript intron_variant - - - - - - rs6538359 12:93219282 T 8411 NM_003566.3 Transcript intron_variant - - - - - - rs7138445 12:93222131 T CCDS31874.1 CCDS31874.1 Transcript intron_variant - - - - - - rs7138445 12:93222131 T 8411 NM_003566.3 Transcript intron_variant - - - - - - rs6538393 12:93586400 T 643339 NR_040096.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7958203 12:93850739 G - - - intergenic_variant - - - - - - rs4296079 12:94263017 A - ENSR00001466056 RegulatoryFeature regulatory_region_variant - - - - - - rs4296079 12:94263017 A - - - intergenic_variant - - - - - - rs4296080 12:94263174 A - - - intergenic_variant - - - - - - rs580871 12:94389815 G - - - intergenic_variant - - - - - - rs2610671 12:94603249 A 10154 NM_005761.2 Transcript intron_variant - - - - - - rs2610671 12:94603249 A ENSESTG00000018762 ENSESTT00000047350 Transcript intron_variant - - - - - - rs2610671 12:94603249 A CCDS9049.1 CCDS9049.1 Transcript intron_variant - - - - - - rs3843644 12:94771462 T ENSESTG00000018907 ENSESTT00000047751 Transcript intron_variant - - - - - - rs3843644 12:94771462 T ENSESTG00000018907 ENSESTT00000047619 Transcript intron_variant - - - - - - rs3843644 12:94771462 T ENSESTG00000018907 ENSESTT00000047790 Transcript intron_variant - - - - - - rs3843644 12:94771462 T 51134 NM_016122.2 Transcript intron_variant - - - - - - rs3843644 12:94771462 T ENSESTG00000018907 ENSESTT00000047793 Transcript intron_variant - - - - - - rs3843644 12:94771462 T CCDS41820.1 CCDS41820.1 Transcript intron_variant - - - - - - rs3843644 12:94771462 T 51134 NM_001042399.1 Transcript intron_variant - - - - - - rs3843644 12:94771462 T ENSESTG00000018907 ENSESTT00000047762 Transcript intron_variant - - - - - - rs2651989 12:94978337 A ENSESTG00000013864 ENSESTT00000034626 Transcript intron_variant - - - - - - rs2651989 12:94978337 A CCDS31877.1 CCDS31877.1 Transcript intron_variant - - - - - - rs2651989 12:94978337 A ENSESTG00000013864 ENSESTT00000034642 Transcript intron_variant - - - - - - rs2651989 12:94978337 A ENSESTG00000013699 ENSESTT00000034228 Transcript intron_variant - - - - - - rs2651989 12:94978337 A 57458 NM_020698.2 Transcript intron_variant - - - - - - rs2367304 12:95673082 A CCDS44954.1 CCDS44954.1 Transcript intron_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034389 Transcript intron_variant - - - - - - rs2367304 12:95673082 A 55591 NM_017599.3 Transcript intron_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034354 Transcript intron_variant - - - - - - rs2367304 12:95673082 A 55591 NR_038241.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2367304 12:95673082 A 55591 NR_038242.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034363 Transcript intron_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034337 Transcript intron_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034351 Transcript intron_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034324 Transcript intron_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034347 Transcript intron_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034311 Transcript intron_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034381 Transcript intron_variant - - - - - - rs2367304 12:95673082 A ENSESTG00000013723 ENSESTT00000034372 Transcript intron_variant - - - - - - rs79188249 12:95975150 G - - - intergenic_variant - - - - - - rs991214 12:96186601 C 59277 NM_021229.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2065 rs991214 12:96186601 C CCDS9054.1 CCDS9054.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2514 rs256188 12:96512114 A - - - intergenic_variant - - - - - - rs7971431 12:96653928 A ENSESTG00000033015 ENSESTT00000083455 Transcript intron_variant - - - - - - rs7971431 12:96653928 A CCDS9060.1 CCDS9060.1 Transcript intron_variant - - - - - - rs7971431 12:96653928 A 2004 NM_005230.2 Transcript intron_variant - - - - - - rs7971431 12:96653928 A ENSESTG00000033015 ENSESTT00000083461 Transcript intron_variant - - - - - - rs10745756 12:96727086 A CCDS9061.1 CCDS9061.1 Transcript intron_variant - - - - - - rs10745756 12:96727086 A 5128 NM_001170464.2 Transcript intron_variant - - - - - - rs10745756 12:96727086 A ENSESTG00000033030 ENSESTT00000083618 Transcript intron_variant - - - - - - rs10745756 12:96727086 A ENSESTG00000033030 ENSESTT00000083612 Transcript intron_variant - - - - - - rs10745756 12:96727086 A ENSESTG00000033030 ENSESTT00000083615 Transcript intron_variant - - - - - - rs10745756 12:96727086 A ENSESTG00000033030 ENSESTT00000083629 Transcript intron_variant - - - - - - rs10745756 12:96727086 A ENSESTG00000033030 ENSESTT00000083600 Transcript intron_variant - - - - - - rs10745756 12:96727086 A CCDS53819.1 CCDS53819.1 Transcript intron_variant - - - - - - rs10745756 12:96727086 A ENSESTG00000033030 ENSESTT00000083624 Transcript intron_variant - - - - - - rs10745756 12:96727086 A 5128 NM_002595.4 Transcript intron_variant - - - - - - rs2887113 12:96841171 A - - - intergenic_variant - - - - - - rs34441 12:97232433 G ENSESTG00000018964 ENSESTT00000047741 Transcript intron_variant - - - - - - rs7953097 12:97364237 G - - - intergenic_variant - - - - - - rs2193013 12:97704408 C - - - intergenic_variant - - - - - - rs10777895 12:98316461 C - ENSR00001466338 RegulatoryFeature regulatory_region_variant - - - - - - rs10777895 12:98316461 C - - - intergenic_variant - - - - - - rs1463225 12:98321272 T - - - intergenic_variant - - - - - - rs2888380 12:99422193 C CCDS55869.1 CCDS55869.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C 56899 NM_001204068.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C 56899 NM_152788.4 Transcript intron_variant - - - - - - rs2888380 12:99422193 C 56899 NM_001204069.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C CCDS55866.1 CCDS55866.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C 56899 NM_181670.3 Transcript intron_variant - - - - - - rs2888380 12:99422193 C CCDS55865.1 CCDS55865.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C CCDS55868.1 CCDS55868.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C CCDS55872.1 CCDS55872.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C 56899 NM_001204067.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C 56899 NM_020140.3 Transcript intron_variant - - - - - - rs2888380 12:99422193 C 56899 NM_001204066.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C CCDS55870.1 CCDS55870.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C CCDS55867.1 CCDS55867.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C 56899 NM_001204070.1 Transcript intron_variant - - - - - - rs2888380 12:99422193 C CCDS55871.1 CCDS55871.1 Transcript intron_variant - - - - - - rs2712651 12:99630449 T 56899 NM_152788.4 Transcript intron_variant - - - - - - rs2712651 12:99630449 T CCDS55872.1 CCDS55872.1 Transcript intron_variant - - - - - - rs2651210 12:99822848 T 56899 NM_152788.4 Transcript intron_variant - - - - - - rs2651210 12:99822848 T CCDS55872.1 CCDS55872.1 Transcript intron_variant - - - - - - rs2724191 12:99835292 A 56899 NM_152788.4 Transcript intron_variant - - - - - - rs2724191 12:99835292 A CCDS55872.1 CCDS55872.1 Transcript intron_variant - - - - - - rs1587502 12:99999155 T ENSESTG00000009027 ENSESTT00000022662 Transcript intron_variant - - - - - - rs1587502 12:99999155 T 56899 NM_152788.4 Transcript intron_variant - - - - - - rs1587502 12:99999155 T CCDS55872.1 CCDS55872.1 Transcript intron_variant - - - - - - rs1587502 12:99999155 T ENSESTG00000009027 ENSESTT00000022672 Transcript intron_variant - - - - - - rs827793 12:100336631 A 56899 NM_152788.4 Transcript intron_variant - - - - - - rs827793 12:100336631 A ENSESTG00000009020 ENSESTT00000022640 Transcript intron_variant - - - - - - rs827793 12:100336631 A CCDS55872.1 CCDS55872.1 Transcript intron_variant - - - - - - rs638615 12:101505216 C CCDS31884.1 CCDS31884.1 Transcript intron_variant - - - - - - rs638615 12:101505216 C 121601 NM_178826.3 Transcript intron_variant - - - - - - rs638615 12:101505216 C ENSESTG00000025646 ENSESTT00000064742 Transcript intron_variant - - - - - - rs2373460 12:101929136 T - - - intergenic_variant - - - - - - rs10745933 12:102338115 G - - - intergenic_variant - - - - - - rs4764859 12:102366150 C - - - intergenic_variant - - - - - - rs4764860 12:102366275 A - - - intergenic_variant - - - - - - rs7295958 12:102427211 C ENSESTG00000020683 ENSESTT00000051896 Transcript intron_variant - - - - - - rs7295958 12:102427211 C CCDS44959.1 CCDS44959.1 Transcript intron_variant - - - - - - rs7295958 12:102427211 C ENSESTG00000020454 ENSESTT00000051283 Transcript intron_variant - - - - - - rs7295958 12:102427211 C 51019 NM_016053.2 Transcript intron_variant - - - - - - rs7308082 12:102428458 T - ENSR00001466544 RegulatoryFeature regulatory_region_variant - - - - - - rs7308082 12:102428458 T ENSESTG00000020683 ENSESTT00000051896 Transcript intron_variant - - - - - - rs7308082 12:102428458 T CCDS44959.1 CCDS44959.1 Transcript intron_variant - - - - - - rs7308082 12:102428458 T ENSESTG00000020454 ENSESTT00000051283 Transcript intron_variant - - - - - - rs7308082 12:102428458 T 51019 NM_016053.2 Transcript intron_variant - - - - - - rs855201 12:102878205 A - ENSR00000090504 RegulatoryFeature regulatory_region_variant - - - - - - rs855201 12:102878205 A 3479 NM_000618.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3827 rs855201 12:102878205 A CCDS44962.1 CCDS44962.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4046 rs855201 12:102878205 A CCDS44961.1 CCDS44961.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4046 rs855201 12:102878205 A CCDS9091.1 CCDS9091.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4046 rs855201 12:102878205 A 3479 NM_001111285.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3827 rs855201 12:102878205 A 3479 NM_001111283.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3827 rs2647868 12:102992651 T - - - intergenic_variant - - - - - - rs2607966 12:103003135 T - - - intergenic_variant - - - - - - rs2643691 12:103005064 C - - - intergenic_variant - - - - - - rs2643690 12:103008055 C - - - intergenic_variant - - - - - - rs2607971 12:103008187 T - - - intergenic_variant - - - - - - rs2643683 12:103017010 G - - - intergenic_variant - - - - - - rs2643682 12:103017312 G - - - intergenic_variant - - - - - - rs2643681 12:103017377 T - - - intergenic_variant - - - - - - rs2643680 12:103017384 T - - - intergenic_variant - - - - - - rs2647883 12:103030735 T - - - intergenic_variant - - - - - - rs2647878 12:103037509 G - - - intergenic_variant - - - - - - rs833714 12:103066666 A - - - intergenic_variant - - - - - - rs7956735 12:103477191 G ENSESTG00000031217 ENSESTT00000078662 Transcript intron_variant - - - - - - rs4764938 12:103505749 C ENSESTG00000031217 ENSESTT00000078662 Transcript intron_variant - - - - - - rs939630 12:103726460 T CCDS44963.1 CCDS44963.1 Transcript intron_variant - - - - - - rs939630 12:103726460 T 374470 NM_001099336.1 Transcript intron_variant - - - - - - rs939630 12:103726460 T ENSESTG00000031187 ENSESTT00000078590 Transcript intron_variant - - - - - - rs939630 12:103726460 T ENSESTG00000031187 ENSESTT00000078574 Transcript intron_variant - - - - - - rs939630 12:103726460 T 374470 NM_198521.2 Transcript intron_variant - - - - - - rs2374051 12:103894540 C 374470 NM_001099336.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4791 rs2374051 12:103894540 C ENSESTG00000031187 ENSESTT00000078590 Transcript upstream_gene_variant - - - - - - DISTANCE=4794 rs2374051 12:103894540 C ENSESTG00000031187 ENSESTT00000078574 Transcript upstream_gene_variant - - - - - - DISTANCE=4791 rs2374051 12:103894540 C 374470 NM_198521.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4794 rs2374051 12:103894540 C ENSESTG00000031187 ENSESTT00000078627 Transcript upstream_gene_variant - - - - - - DISTANCE=4816 rs1650122 12:104095640 G CCDS31888.1 CCDS31888.1 Transcript intron_variant - - - - - - rs1650122 12:104095640 G ENSESTG00000023706 ENSESTT00000059781 Transcript intron_variant - - - - - - rs1650122 12:104095640 G ENSESTG00000023725 ENSESTT00000059803 Transcript upstream_gene_variant - - - - - - DISTANCE=1373 rs1650122 12:104095640 G ENSESTG00000023725 ENSESTT00000059831 Transcript upstream_gene_variant - - - - - - DISTANCE=2703 rs1650122 12:104095640 G 55576 NM_017564.9 Transcript intron_variant - - - - - - rs1882502 12:104826694 G - - - intergenic_variant - - - - - - rs4964291 12:104851965 C - ENSR00000436127 RegulatoryFeature regulatory_region_variant - - - - - - rs4964291 12:104851965 C 50515 NM_001173982.1 Transcript intron_variant - - - - - - rs4964291 12:104851965 C CCDS9099.1 CCDS9099.1 Transcript intron_variant - - - - - - rs4964291 12:104851965 C CCDS55878.1 CCDS55878.1 Transcript intron_variant - - - - - - rs4964291 12:104851965 C 50515 NM_018413.5 Transcript intron_variant - - - - - - rs4964291 12:104851965 C ENSESTG00000024707 ENSESTT00000062479 Transcript intron_variant - - - - - - rs4964291 12:104851965 C ENSESTG00000024707 ENSESTT00000062510 Transcript intron_variant - - - - - - rs7975558 12:104881557 G 50515 NM_001173982.1 Transcript intron_variant - - - - - - rs7975558 12:104881557 G CCDS9099.1 CCDS9099.1 Transcript intron_variant - - - - - - rs7975558 12:104881557 G CCDS55878.1 CCDS55878.1 Transcript intron_variant - - - - - - rs7975558 12:104881557 G 50515 NM_018413.5 Transcript intron_variant - - - - - - rs7975558 12:104881557 G ENSESTG00000024707 ENSESTT00000062479 Transcript intron_variant - - - - - - rs7975558 12:104881557 G ENSESTG00000024707 ENSESTT00000062510 Transcript intron_variant - - - - - - rs2463445 12:105181903 A - - - intergenic_variant - - - - - - rs2453162 12:105218582 C ENSESTG00000021921 ENSESTT00000055212 Transcript intron_variant - - - - - - rs2453162 12:105218582 C ENSESTG00000021921 ENSESTT00000055255 Transcript intron_variant - - - - - - rs2453162 12:105218582 C CCDS9100.2 CCDS9100.2 Transcript intron_variant - - - - - - rs2453162 12:105218582 C ENSESTG00000021921 ENSESTT00000055192 Transcript intron_variant - - - - - - rs2453162 12:105218582 C ENSESTG00000021921 ENSESTT00000055231 Transcript intron_variant - - - - - - rs2453162 12:105218582 C ENSESTG00000021921 ENSESTT00000055283 Transcript intron_variant - - - - - - rs2453162 12:105218582 C ENSESTG00000021921 ENSESTT00000055293 Transcript intron_variant - - - - - - rs2453162 12:105218582 C 84102 NM_032148.3 Transcript intron_variant - - - - - - rs10778359 12:105359494 A - - - intergenic_variant - - - - - - rs2464172 12:105544131 T CCDS41826.1 CCDS41826.1 Transcript intron_variant - - - - - - rs2464172 12:105544131 T ENSESTG00000021657 ENSESTT00000054597 Transcript intron_variant - - - - - - rs2464172 12:105544131 T 23325 NM_015275.1 Transcript intron_variant - - - - - - rs2464172 12:105544131 T ENSESTG00000021657 ENSESTT00000054589 Transcript intron_variant - - - - - - rs2464172 12:105544131 T ENSESTG00000021657 ENSESTT00000054582 Transcript intron_variant - - - - - - rs2464172 12:105544131 T ENSESTG00000021657 ENSESTT00000054571 Transcript intron_variant - - - - - - rs2464189 12:105549840 C CCDS41826.1 CCDS41826.1 Transcript intron_variant - - - - - - rs2464189 12:105549840 C 23325 NM_015275.1 Transcript intron_variant - - - - - - rs2464189 12:105549840 C ENSESTG00000021657 ENSESTT00000054589 Transcript intron_variant - - - - - - rs2464189 12:105549840 C ENSESTG00000021657 ENSESTT00000054613 Transcript 5_prime_UTR_variant 197 - - - - - rs2464189 12:105549840 C ENSESTG00000021657 ENSESTT00000054597 Transcript downstream_gene_variant - - - - - - DISTANCE=3607 rs2464189 12:105549840 C ENSESTG00000021657 ENSESTT00000054582 Transcript intron_variant - - - - - - rs2464189 12:105549840 C ENSESTG00000021657 ENSESTT00000054619 Transcript 5_prime_UTR_variant 197 - - - - - rs2464189 12:105549840 C ENSESTG00000021657 ENSESTT00000054571 Transcript intron_variant - - - - - - rs2464186 12:105585666 T CCDS58275.1 CCDS58275.1 Transcript intron_variant - - - - - - rs2464186 12:105585666 T 55198 NM_001251905.1 Transcript intron_variant - - - - - - rs2464186 12:105585666 T 55198 NM_018171.3 Transcript intron_variant - - - - - - rs2464186 12:105585666 T CCDS58276.1 CCDS58276.1 Transcript intron_variant - - - - - - rs2464186 12:105585666 T ENSESTG00000021890 ENSESTT00000055058 Transcript upstream_gene_variant - - - - - - DISTANCE=1874 rs2464186 12:105585666 T ENSESTG00000021821 ENSESTT00000055018 Transcript intron_variant - - - - - - rs2464186 12:105585666 T ENSESTG00000021821 ENSESTT00000054962 Transcript intron_variant - - - - - - rs2464186 12:105585666 T CCDS9101.1 CCDS9101.1 Transcript intron_variant - - - - - - rs2464186 12:105585666 T 55198 NM_001251904.1 Transcript intron_variant - - - - - - rs2440699 12:105586063 C CCDS58275.1 CCDS58275.1 Transcript intron_variant - - - - - - rs2440699 12:105586063 C 55198 NM_001251905.1 Transcript intron_variant - - - - - - rs2440699 12:105586063 C 55198 NM_018171.3 Transcript intron_variant - - - - - - rs2440699 12:105586063 C CCDS58276.1 CCDS58276.1 Transcript intron_variant - - - - - - rs2440699 12:105586063 C ENSESTG00000021890 ENSESTT00000055058 Transcript upstream_gene_variant - - - - - - DISTANCE=2271 rs2440699 12:105586063 C ENSESTG00000021821 ENSESTT00000055018 Transcript intron_variant - - - - - - rs2440699 12:105586063 C ENSESTG00000021821 ENSESTT00000054962 Transcript intron_variant - - - - - - rs2440699 12:105586063 C CCDS9101.1 CCDS9101.1 Transcript intron_variant - - - - - - rs2440699 12:105586063 C 55198 NM_001251904.1 Transcript intron_variant - - - - - - rs2440698 12:105586221 A CCDS58275.1 CCDS58275.1 Transcript intron_variant - - - - - - rs2440698 12:105586221 A 55198 NM_001251905.1 Transcript intron_variant - - - - - - rs2440698 12:105586221 A 55198 NM_018171.3 Transcript intron_variant - - - - - - rs2440698 12:105586221 A CCDS58276.1 CCDS58276.1 Transcript intron_variant - - - - - - rs2440698 12:105586221 A ENSESTG00000021890 ENSESTT00000055058 Transcript upstream_gene_variant - - - - - - DISTANCE=2429 rs2440698 12:105586221 A ENSESTG00000021821 ENSESTT00000055018 Transcript intron_variant - - - - - - rs2440698 12:105586221 A ENSESTG00000021821 ENSESTT00000054962 Transcript intron_variant - - - - - - rs2440698 12:105586221 A CCDS9101.1 CCDS9101.1 Transcript intron_variant - - - - - - rs2440698 12:105586221 A 55198 NM_001251904.1 Transcript intron_variant - - - - - - rs12580666 12:105795199 G - - - intergenic_variant - - - - - - rs1834870 12:106454205 T 9891 NM_014840.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2920 rs1234972 12:106913498 T - ENSR00000436469 RegulatoryFeature regulatory_region_variant - - - - - - rs1234972 12:106913498 T 100287944 NR_040246.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10778486 12:106931027 A 100287944 NR_040246.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1964329 12:106990110 A 5992 NM_001206691.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4805 rs1964329 12:106990110 A ENSESTG00000008951 ENSESTT00000022542 Transcript intron_variant - - - - - - rs1964329 12:106990110 A ENSESTG00000008951 ENSESTT00000022471 Transcript intron_variant - - - - - - rs1964329 12:106990110 A CCDS9106.1 CCDS9106.1 Transcript intron_variant - - - - - - rs1964329 12:106990110 A ENSESTG00000008951 ENSESTT00000022550 Transcript upstream_gene_variant - - - - - - DISTANCE=4834 rs1964329 12:106990110 A CCDS55880.1 CCDS55880.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4945 rs1964329 12:106990110 A 5992 NM_213594.2 Transcript intron_variant - - - - - - rs1964329 12:106990110 A ENSESTG00000008951 ENSESTT00000022479 Transcript intron_variant - - - - - - rs1964329 12:106990110 A 100287944 NR_040246.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3953611 12:107533450 T - - - intergenic_variant - - - - - - rs7300407 12:107649687 G - - - intergenic_variant - - - - - - rs7971174 12:108247500 A - - - intergenic_variant - - - - - - rs1529327 12:108661223 C - - - intergenic_variant - - - - - - rs4964250 12:108737663 T ENSESTG00000003572 ENSESTT00000008942 Transcript upstream_gene_variant - - - - - - DISTANCE=4569 rs4964250 12:108737663 T 1240 NM_004072.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4569 rs4964250 12:108737663 T 1240 NM_001142343.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4569 rs4964250 12:108737663 T 1240 NM_001142344.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4569 rs1184148 12:108921602 G CCDS9117.1 CCDS9117.1 Transcript intron_variant - - - - - - rs1184148 12:108921602 G ENSESTG00000010651 ENSESTT00000026709 Transcript intron_variant - - - - - - rs1184148 12:108921602 G ENSESTG00000010372 ENSESTT00000025963 Transcript downstream_gene_variant - - - - - - DISTANCE=1990 rs1184148 12:108921602 G ENSESTG00000010390 ENSESTT00000025998 Transcript upstream_gene_variant - - - - - - DISTANCE=4342 rs1184148 12:108921602 G 9733 NM_014706.3 Transcript intron_variant - - - - - - rs1184148 12:108921602 G ENSESTG00000010372 ENSESTT00000025943 Transcript downstream_gene_variant - - - - - - DISTANCE=1991 rs1861995 12:109193613 G ENSESTG00000010619 ENSESTT00000026569 Transcript intron_variant - - - - - - rs1861995 12:109193613 G CCDS55882.1 CCDS55882.1 Transcript intron_variant - - - - - - rs1861995 12:109193613 G CCDS53825.1 CCDS53825.1 Transcript intron_variant - - - - - - rs1861995 12:109193613 G 54434 NM_018984.3 Transcript intron_variant - - - - - - rs1861995 12:109193613 G 54434 NM_001161331.1 Transcript intron_variant - - - - - - rs1861995 12:109193613 G CCDS9121.1 CCDS9121.1 Transcript intron_variant - - - - - - rs1861995 12:109193613 G 54434 NM_001161330.1 Transcript intron_variant - - - - - - rs147033787 12:109356464 G ENSESTG00000010590 ENSESTT00000026532 Transcript intron_variant - - - - - - rs147033787 12:109356464 G ENSESTG00000010590 ENSESTT00000026527 Transcript intron_variant - - - - - - rs147033787 12:109356464 G 55530 NM_018711.2 Transcript intron_variant - - - - - - rs77177844 12:109446859 C ENSESTG00000010590 ENSESTT00000026532 Transcript intron_variant - - - - - - rs77177844 12:109446859 C ENSESTG00000010590 ENSESTT00000026527 Transcript intron_variant - - - - - - rs6606701 12:109779781 A - - - intergenic_variant - - - - - - rs1362654 12:110047098 C - - - intergenic_variant - - - - - - rs6416329 12:111276746 T - - - intergenic_variant - - - - - - rs11065795 12:111497066 G CCDS41837.1 CCDS41837.1 Transcript intron_variant - - - - - - rs11065795 12:111497066 G 23316 NM_015267.3 Transcript intron_variant - - - - - - rs4766541 12:111586446 G CCDS41837.1 CCDS41837.1 Transcript intron_variant - - - - - - rs4766541 12:111586446 G 23316 NM_015267.3 Transcript intron_variant - - - - - - rs6490144 12:111904703 G ENSESTG00000033118 ENSESTT00000083758 Transcript intron_variant - - - - - - rs6490144 12:111904703 G ENSESTG00000033118 ENSESTT00000083797 Transcript intron_variant - - - - - - rs6490144 12:111904703 G 6311 NM_002973.3 Transcript intron_variant - - - - - - rs6490144 12:111904703 G ENSESTG00000033118 ENSESTT00000083788 Transcript intron_variant - - - - - - rs6490144 12:111904703 G CCDS31902.1 CCDS31902.1 Transcript intron_variant - - - - - - rs6490144 12:111904703 G ENSESTG00000033118 ENSESTT00000083790 Transcript intron_variant - - - - - - rs6490144 12:111904703 G ENSESTG00000033118 ENSESTT00000083800 Transcript intron_variant - - - - - - rs6490144 12:111904703 G ENSESTG00000033118 ENSESTT00000083759 Transcript intron_variant - - - - - - rs6490144 12:111904703 G ENSESTG00000033118 ENSESTT00000083799 Transcript intron_variant - - - - - - rs6490144 12:111904703 G ENSESTG00000033118 ENSESTT00000083784 Transcript intron_variant - - - - - - rs757163 12:112673785 G ENSESTG00000032741 ENSESTT00000082719 Transcript downstream_gene_variant - - - - - - DISTANCE=3083 rs757163 12:112673785 G ENSESTG00000032751 ENSESTT00000082740 Transcript intron_variant - - - - - - rs757163 12:112673785 G ENSESTG00000032766 ENSESTT00000082778 Transcript upstream_gene_variant - - - - - - DISTANCE=4444 rs757163 12:112673785 G 283450 NM_001109662.3 Transcript intron_variant - - - - - - rs6489845 12:112958220 C - - - intergenic_variant - - - - - - rs1024466 12:113186931 G - - - intergenic_variant - - - - - - rs7309428 12:113389111 T ENSESTG00000025744 ENSESTT00000065010 Transcript intron_variant - - - - - - rs7309428 12:113389111 T CCDS44981.1 CCDS44981.1 Transcript intron_variant - - - - - - rs7309428 12:113389111 T ENSESTG00000025744 ENSESTT00000065017 Transcript intron_variant - - - - - - rs7309428 12:113389111 T ENSESTG00000025744 ENSESTT00000065026 Transcript intron_variant - - - - - - rs7309428 12:113389111 T 4940 NM_006187.2 Transcript intron_variant - - - - - - rs7309428 12:113389111 T ENSESTG00000025744 ENSESTT00000064992 Transcript intron_variant - - - - - - rs1895982 12:113963708 C - - - intergenic_variant - - - - - - rs595218 12:114130011 G - - - intergenic_variant - - - - - - rs249044 12:114158204 T - - - intergenic_variant - - - - - - rs7967607 12:114280459 C ENSESTG00000034735 ENSESTT00000087854 Transcript intron_variant - - - - - - rs7967607 12:114280459 C ENSESTG00000034735 ENSESTT00000087849 Transcript intron_variant - - - - - - rs7967607 12:114280459 C ENSESTG00000034735 ENSESTT00000087860 Transcript intron_variant - - - - - - rs7967607 12:114280459 C CCDS9172.1 CCDS9172.1 Transcript intron_variant - - - - - - rs7967607 12:114280459 C 9904 NM_001146698.1 Transcript intron_variant - - - - - - rs7967607 12:114280459 C 9904 NM_001146699.1 Transcript intron_variant - - - - - - rs7967607 12:114280459 C ENSESTG00000034735 ENSESTT00000087865 Transcript intron_variant - - - - - - rs7967607 12:114280459 C ENSESTG00000034735 ENSESTT00000087812 Transcript intron_variant - - - - - - rs7967607 12:114280459 C 9904 NM_016196.3 Transcript intron_variant - - - - - - rs7967607 12:114280459 C ENSESTG00000034735 ENSESTT00000087858 Transcript intron_variant - - - - - - rs7967607 12:114280459 C ENSESTG00000034735 ENSESTT00000087871 Transcript intron_variant - - - - - - rs7967607 12:114280459 C ENSESTG00000034735 ENSESTT00000087856 Transcript intron_variant - - - - - - rs4238036 12:114343676 G ENSESTG00000034735 ENSESTT00000087854 Transcript intron_variant - - - - - - rs4238036 12:114343676 G ENSESTG00000034735 ENSESTT00000087849 Transcript intron_variant - - - - - - rs4238036 12:114343676 G ENSESTG00000034735 ENSESTT00000087860 Transcript intron_variant - - - - - - rs4238036 12:114343676 G CCDS9172.1 CCDS9172.1 Transcript intron_variant - - - - - - rs4238036 12:114343676 G 9904 NM_001146698.1 Transcript intron_variant - - - - - - rs4238036 12:114343676 G 9904 NM_001146699.1 Transcript intron_variant - - - - - - rs4238036 12:114343676 G ENSESTG00000034735 ENSESTT00000087865 Transcript intron_variant - - - - - - rs4238036 12:114343676 G ENSESTG00000034735 ENSESTT00000087812 Transcript intron_variant - - - - - - rs4238036 12:114343676 G 9904 NM_016196.3 Transcript intron_variant - - - - - - rs4238036 12:114343676 G ENSESTG00000034735 ENSESTT00000087858 Transcript intron_variant - - - - - - rs4238036 12:114343676 G ENSESTG00000034735 ENSESTT00000087856 Transcript intron_variant - - - - - - rs3108468 12:114343757 A ENSESTG00000034735 ENSESTT00000087854 Transcript intron_variant - - - - - - rs3108468 12:114343757 A ENSESTG00000034735 ENSESTT00000087849 Transcript intron_variant - - - - - - rs3108468 12:114343757 A ENSESTG00000034735 ENSESTT00000087860 Transcript intron_variant - - - - - - rs3108468 12:114343757 A CCDS9172.1 CCDS9172.1 Transcript intron_variant - - - - - - rs3108468 12:114343757 A 9904 NM_001146698.1 Transcript intron_variant - - - - - - rs3108468 12:114343757 A 9904 NM_001146699.1 Transcript intron_variant - - - - - - rs3108468 12:114343757 A ENSESTG00000034735 ENSESTT00000087865 Transcript intron_variant - - - - - - rs3108468 12:114343757 A ENSESTG00000034735 ENSESTT00000087812 Transcript intron_variant - - - - - - rs3108468 12:114343757 A 9904 NM_016196.3 Transcript intron_variant - - - - - - rs3108468 12:114343757 A ENSESTG00000034735 ENSESTT00000087858 Transcript intron_variant - - - - - - rs3108468 12:114343757 A ENSESTG00000034735 ENSESTT00000087856 Transcript intron_variant - - - - - - rs1896011 12:114737834 T - - - intergenic_variant - - - - - - rs2912457 12:114800804 G CCDS9173.1 CCDS9173.1 Transcript intron_variant - - - - - - rs2912457 12:114800804 G 6910 NM_080717.2 Transcript intron_variant - - - - - - rs2912457 12:114800804 G CCDS9174.1 CCDS9174.1 Transcript intron_variant - - - - - - rs2912457 12:114800804 G 6910 NM_181486.2 Transcript intron_variant - - - - - - rs2912457 12:114800804 G 6910 NM_000192.3 Transcript intron_variant - - - - - - rs1248040 12:114888875 T - - - intergenic_variant - - - - - - rs1248043 12:114927524 A - - - intergenic_variant - - - - - - rs1248044 12:114933971 C - - - intergenic_variant - - - - - - rs864510 12:114945137 G - - - intergenic_variant - - - - - - rs1566644 12:115206656 C - - - intergenic_variant - - - - - - rs10774770 12:115238613 C - ENSR00000437510 RegulatoryFeature regulatory_region_variant - - - - - - rs10774770 12:115238613 C - - - intergenic_variant - - - - - - rs6489986 12:115339575 C - - - intergenic_variant - - - - - - rs1233041 12:115600302 G - - - intergenic_variant - - - - - - rs7310789 12:115786039 A - - - intergenic_variant - - - - - - rs1270730 12:116292031 A - - - intergenic_variant - - - - - - rs7134183 12:116575323 G ENSESTG00000008574 ENSESTT00000021565 Transcript intron_variant - - - - - - rs7134183 12:116575323 G CCDS9177.1 CCDS9177.1 Transcript intron_variant - - - - - - rs7134183 12:116575323 G 23389 NM_015335.4 Transcript intron_variant - - - - - - rs10774846 12:116739944 G - - - intergenic_variant - - - - - - rs622688 12:118118131 C - ENSR00000437860 RegulatoryFeature regulatory_region_variant - - - - - - rs622688 12:118118131 C 283455 NM_173598.4 Transcript intron_variant - - - - - - rs2682772 12:119027960 C - - - intergenic_variant - - - - - - rs784854 12:119897694 T ENSESTG00000019038 ENSESTT00000047881 Transcript intron_variant - - - - - - rs784854 12:119897694 T ENSESTG00000019038 ENSESTT00000047869 Transcript intron_variant - - - - - - rs784854 12:119897694 T CCDS9190.1 CCDS9190.1 Transcript intron_variant - - - - - - rs784854 12:119897694 T 160777 NM_178499.3 Transcript intron_variant - - - - - - rs784854 12:119897694 T ENSESTG00000019038 ENSESTT00000047894 Transcript intron_variant - - - - - - rs784854 12:119897694 T ENSESTG00000019008 ENSESTT00000047804 Transcript intron_variant - - - - - - rs615298 12:120925963 G - ENSR00000438153 RegulatoryFeature regulatory_region_variant - - - - - - rs615298 12:120925963 G 100506668 NR_038854.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2178 rs615298 12:120925963 G 8655 NM_001037494.1 Transcript intron_variant - - - - - - rs568055 12:120981047 T ENSESTG00000034775 ENSESTT00000087953 Transcript intron_variant - - - - - - rs568055 12:120981047 T ENSESTG00000034775 ENSESTT00000088051 Transcript intron_variant - - - - - - rs568055 12:120981047 T 9921 NM_014868.4 Transcript intron_variant - - - - - - rs568055 12:120981047 T ENSESTG00000034775 ENSESTT00000087958 Transcript intron_variant - - - - - - rs568055 12:120981047 T ENSESTG00000034775 ENSESTT00000088052 Transcript intron_variant - - - - - - rs568055 12:120981047 T ENSESTG00000035080 ENSESTT00000088669 Transcript intron_variant - - - - - - rs568055 12:120981047 T ENSESTG00000034775 ENSESTT00000088011 Transcript intron_variant - - - - - - rs568055 12:120981047 T CCDS9201.1 CCDS9201.1 Transcript intron_variant - - - - - - rs568055 12:120981047 T ENSESTG00000034775 ENSESTT00000088009 Transcript intron_variant - - - - - - rs568055 12:120981047 T ENSESTG00000034775 ENSESTT00000088044 Transcript intron_variant - - - - - - rs646109 12:121301924 T CCDS9208.1 CCDS9208.1 Transcript intron_variant - - - - - - rs646109 12:121301924 T ENSESTG00000035056 ENSESTT00000088623 Transcript intron_variant - - - - - - rs646109 12:121301924 T 121665 NM_139015.4 Transcript intron_variant - - - - - - rs2952660 12:121558720 G - - - intergenic_variant - - - - - - rs28547203 12:121980541 G ENSESTG00000028588 ENSESTT00000071979 Transcript intron_variant - - - - - - rs28547203 12:121980541 G 84678 NM_032590.4 Transcript intron_variant - - - - - - rs28547203 12:121980541 G 84678 NM_001005366.1 Transcript intron_variant - - - - - - rs28547203 12:121980541 G CCDS41849.1 CCDS41849.1 Transcript intron_variant - - - - - - rs28547203 12:121980541 G ENSESTG00000028588 ENSESTT00000071961 Transcript intron_variant - - - - - - rs28547203 12:121980541 G CCDS41850.1 CCDS41850.1 Transcript intron_variant - - - - - - rs28547203 12:121980541 G ENSESTG00000028588 ENSESTT00000071991 Transcript intron_variant - - - - - - rs7398439 12:122075664 G - ENSR00000174313 RegulatoryFeature regulatory_region_variant - - - - - - rs7398439 12:122075664 G 84876 NM_032790.3 Transcript intron_variant - - - - - - rs7398439 12:122075664 G CCDS41851.1 CCDS41851.1 Transcript intron_variant - - - - - - rs7398439 12:122075664 G ENSESTG00000035399 ENSESTT00000089392 Transcript intron_variant - - - - - - rs2936765 12:123165583 T - - - intergenic_variant - - - - - - rs10846619 12:124664828 C - ENSR00001468051 RegulatoryFeature regulatory_region_variant - - - - - - rs10846619 12:124664828 C ENSESTG00000022567 ENSESTT00000057057 Transcript intron_variant - - - - - - rs10846619 12:124664828 C 100533183 NM_001204299.1 Transcript intron_variant - - - - - - rs10744170 12:124692731 G ENSESTG00000022567 ENSESTT00000057057 Transcript intron_variant - - - - - - rs10744170 12:124692731 G 100533183 NM_001204299.1 Transcript intron_variant - - - - - - rs837940 12:125107092 C - - - intergenic_variant - - - - - - rs7969543 12:125138554 T - - - intergenic_variant - - - - - - rs7137123 12:125397750 G - ENSR00001468150 RegulatoryFeature regulatory_region_variant - - - - - - rs7137123 12:125397750 G ENSESTG00000021100 ENSESTT00000052988 Transcript downstream_gene_variant - - - - - - DISTANCE=67 rs7137123 12:125397750 G 7316 NM_021009.5 Transcript missense_variant 1026 568 190 S/P Tct/Cct - PolyPhen=unknown;SIFT=tolerated rs7137123 12:125397750 G 100847004 NR_049820.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2343 rs7137123 12:125397750 G ENSESTG00000021100 ENSESTT00000053016 Transcript intron_variant - - - - - - rs7137123 12:125397750 G ENSESTG00000021100 ENSESTT00000052937 Transcript downstream_gene_variant - - - - - - DISTANCE=293 rs7137123 12:125397750 G CCDS9260.1 CCDS9260.1 Transcript missense_variant 568 568 190 S/P Tct/Cct - PolyPhen=unknown;SIFT=tolerated rs976834 12:126075405 A ENSESTG00000017091 ENSESTT00000042952 Transcript intron_variant - - - - - - rs976834 12:126075405 A CCDS41859.1 CCDS41859.1 Transcript intron_variant - - - - - - rs976834 12:126075405 A 114795 NM_052907.2 Transcript intron_variant - - - - - - rs2109146 12:126932224 G - ENSR00000439111 RegulatoryFeature regulatory_region_variant - - - - - - rs2109146 12:126932224 G 100128554 NR_015398.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2109434 12:127063913 G - - - intergenic_variant - - - - - - rs1147249 12:127383932 C - - - intergenic_variant - - - - - - rs1672291 12:127434905 G - ENSR00000654824 RegulatoryFeature regulatory_region_variant - - - - - - rs1672291 12:127434905 G - - - intergenic_variant - - - - - - rs1672280 12:127446567 T - - - intergenic_variant - - - - - - rs2605470 12:127478595 C ENSESTG00000004466 ENSESTT00000011275 Transcript intron_variant - - - - - - rs7980307 12:127547632 G ENSESTG00000004466 ENSESTT00000011275 Transcript upstream_gene_variant - - - - - - DISTANCE=2686 rs7980307 12:127547632 G ENSESTG00000004456 ENSESTT00000011235 Transcript downstream_gene_variant - - - - - - DISTANCE=623 rs7980307 12:127547632 G ENSESTG00000004466 ENSESTT00000011278 Transcript upstream_gene_variant - - - - - - DISTANCE=2738 rs10444462 12:127734681 C - - - intergenic_variant - - - - - - rs906733 12:127761830 G ENSESTG00000004460 ENSESTT00000011248 Transcript intron_variant - - - - - - rs906733 12:127761830 G ENSESTG00000004460 ENSESTT00000011251 Transcript upstream_gene_variant - - - - - - DISTANCE=1709 rs1700404 12:127908403 A - ENSR00001468301 RegulatoryFeature regulatory_region_variant - - - - - - rs1700404 12:127908403 A - - - intergenic_variant - - - - - - rs1879392 12:127910695 T - - - intergenic_variant - - - - - - rs1612234 12:128886950 C 92293 NM_001136103.2 Transcript intron_variant - - - - - - rs1612234 12:128886950 C ENSESTG00000033321 ENSESTT00000084159 Transcript intron_variant - - - - - - rs1683722 12:128893959 A 92293 NM_001136103.2 Transcript intron_variant - - - - - - rs1683722 12:128893959 A ENSESTG00000033321 ENSESTT00000084159 Transcript downstream_gene_variant - - - - - - DISTANCE=4600 rs1673962 12:128931342 G 92293 NM_001136103.2 Transcript intron_variant - - - - - - rs673474 12:129436544 G ENSESTG00000033358 ENSESTT00000084230 Transcript intron_variant - - - - - - rs673474 12:129436544 G 144423 NM_144669.1 Transcript intron_variant - - - - - - rs673474 12:129436544 G CCDS9265.1 CCDS9265.1 Transcript intron_variant - - - - - - rs470814 12:129448494 C ENSESTG00000033358 ENSESTT00000084230 Transcript intron_variant - - - - - - rs470814 12:129448494 C 144423 NM_144669.1 Transcript intron_variant - - - - - - rs470814 12:129448494 C CCDS9265.1 CCDS9265.1 Transcript intron_variant - - - - - - rs470858 12:129465292 C ENSESTG00000033358 ENSESTT00000084230 Transcript intron_variant - - - - - - rs470858 12:129465292 C 144423 NM_144669.1 Transcript intron_variant - - - - - - rs470858 12:129465292 C CCDS9265.1 CCDS9265.1 Transcript intron_variant - - - - - - rs11060060 12:129477212 C - - - intergenic_variant - - - - - - rs470383 12:129478442 C - - - intergenic_variant - - - - - - rs470394 12:129480649 G - - - intergenic_variant - - - - - - rs470408 12:129486616 C - - - intergenic_variant - - - - - - rs494883 12:129499869 C - - - intergenic_variant - - - - - - rs561555 12:129506509 G - - - intergenic_variant - - - - - - rs6486769 12:129576149 T CCDS9266.1 CCDS9266.1 Transcript intron_variant - - - - - - rs6486769 12:129576149 T 121256 NM_133448.2 Transcript intron_variant - - - - - - rs10847817 12:129732938 A CCDS9266.1 CCDS9266.1 Transcript intron_variant - - - - - - rs10847817 12:129732938 A 121256 NM_133448.2 Transcript intron_variant - - - - - - rs4759571 12:129936791 G ENSESTG00000002017 ENSESTT00000005018 Transcript downstream_gene_variant - - - - - - DISTANCE=2416 rs4759571 12:129936791 G CCDS9266.1 CCDS9266.1 Transcript intron_variant - - - - - - rs4759571 12:129936791 G 121256 NM_133448.2 Transcript intron_variant - - - - - - rs656483 12:130151679 G ENSESTG00000002005 ENSESTT00000004995 Transcript intron_variant - - - - - - rs656483 12:130151679 G CCDS9266.1 CCDS9266.1 Transcript intron_variant - - - - - - rs656483 12:130151679 G 121256 NM_133448.2 Transcript intron_variant - - - - - - rs264484 12:130178111 C ENSESTG00000002005 ENSESTT00000004995 Transcript intron_variant - - - - - - rs264484 12:130178111 C ENSESTG00000002011 ENSESTT00000004999 Transcript intron_variant - - - - - - rs264484 12:130178111 C CCDS9266.1 CCDS9266.1 Transcript intron_variant - - - - - - rs264484 12:130178111 C 121256 NM_133448.2 Transcript intron_variant - - - - - - rs4237839 12:130214126 C CCDS9266.1 CCDS9266.1 Transcript intron_variant - - - - - - rs4237839 12:130214126 C 121256 NM_133448.2 Transcript intron_variant - - - - - - rs1451910 12:130259937 C CCDS9266.1 CCDS9266.1 Transcript intron_variant - - - - - - rs1451910 12:130259937 C 121256 NM_133448.2 Transcript intron_variant - - - - - - rs1798305 12:130778084 T - - - intergenic_variant - - - - - - rs1828945 12:131037406 T - ENSR00001468450 RegulatoryFeature regulatory_region_variant - - - - - - rs1828945 12:131037406 T ENSESTG00000003316 ENSESTT00000008255 Transcript intron_variant - - - - - - rs1195590 12:131193719 G ENSESTG00000003316 ENSESTT00000008255 Transcript intron_variant - - - - - - rs1881065 12:131256898 C - - - intergenic_variant - - - - - - rs1195588 12:131265891 G - - - intergenic_variant - - - - - - rs7966736 12:131658186 C 116437 NR_026670.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs7965611 12:132323089 G CCDS31927.1 CCDS31927.1 Transcript intron_variant - - - - - - rs7965611 12:132323089 G ENSESTG00000001534 ENSESTT00000003630 Transcript intron_variant - - - - - - rs7965611 12:132323089 G ENSESTG00000001534 ENSESTT00000003635 Transcript intron_variant - - - - - - rs7965611 12:132323089 G 4326 NM_016155.4 Transcript intron_variant - - - - - - rs10751705 12:132336317 G CCDS31927.1 CCDS31927.1 Transcript downstream_gene_variant - - - - - - DISTANCE=498 rs10751705 12:132336317 G ENSESTG00000001534 ENSESTT00000003643 Transcript downstream_gene_variant - - - - - - DISTANCE=538 rs10751705 12:132336317 G ENSESTG00000001534 ENSESTT00000003630 Transcript downstream_gene_variant - - - - - - DISTANCE=440 rs10751705 12:132336317 G ENSESTG00000001534 ENSESTT00000003635 Transcript downstream_gene_variant - - - - - - DISTANCE=440 rs10751705 12:132336317 G 4326 NM_016155.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1 rs4964932 12:132337617 A - ENSR00000247378 RegulatoryFeature regulatory_region_variant - - - - - - rs4964932 12:132337617 A CCDS31927.1 CCDS31927.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1798 rs4964932 12:132337617 A ENSESTG00000001534 ENSESTT00000003643 Transcript downstream_gene_variant - - - - - - DISTANCE=1838 rs4964932 12:132337617 A ENSESTG00000001534 ENSESTT00000003630 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs4964932 12:132337617 A ENSESTG00000001534 ENSESTT00000003635 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs4964932 12:132337617 A 4326 NM_016155.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1301 rs6598166 12:132339101 G CCDS31927.1 CCDS31927.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3282 rs6598166 12:132339101 G ENSESTG00000001534 ENSESTT00000003643 Transcript downstream_gene_variant - - - - - - DISTANCE=3322 rs6598166 12:132339101 G ENSESTG00000001534 ENSESTT00000003630 Transcript downstream_gene_variant - - - - - - DISTANCE=3224 rs6598166 12:132339101 G ENSESTG00000001534 ENSESTT00000003635 Transcript downstream_gene_variant - - - - - - DISTANCE=3224 rs6598166 12:132339101 G 4326 NM_016155.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2785 rs10736912 12:132351723 A - - - intergenic_variant - - - - - - rs56160631 12:132352282 G - - - intergenic_variant - - - - - - rs4964915 12:132405523 C ENSESTG00000001551 ENSESTT00000003715 Transcript downstream_gene_variant - - - - - - DISTANCE=2306 rs4964915 12:132405523 C 8408 NM_003565.2 Transcript intron_variant - - - - - - rs4964915 12:132405523 C ENSESTG00000001578 ENSESTT00000003756 Transcript intron_variant - - - - - - rs4964915 12:132405523 C ENSESTG00000001578 ENSESTT00000003763 Transcript intron_variant - - - - - - rs4964915 12:132405523 C ENSESTG00000001551 ENSESTT00000003723 Transcript intron_variant - - - - - - rs4964915 12:132405523 C CCDS9274.1 CCDS9274.1 Transcript intron_variant - - - - - - rs4964915 12:132405523 C ENSESTG00000001551 ENSESTT00000003717 Transcript downstream_gene_variant - - - - - - DISTANCE=2306 rs4964915 12:132405523 C ENSESTG00000001787 ENSESTT00000004378 Transcript downstream_gene_variant - - - - - - DISTANCE=3539 rs7311029 12:132406275 C ENSESTG00000001551 ENSESTT00000003715 Transcript downstream_gene_variant - - - - - - DISTANCE=3058 rs7311029 12:132406275 C 8408 NM_003565.2 Transcript 3_prime_UTR_variant 3790 - - - - - rs7311029 12:132406275 C ENSESTG00000001578 ENSESTT00000003756 Transcript downstream_gene_variant - - - - - - DISTANCE=132 rs7311029 12:132406275 C ENSESTG00000001578 ENSESTT00000003763 Transcript 3_prime_UTR_variant 332 - - - - - rs7311029 12:132406275 C ENSESTG00000001551 ENSESTT00000003723 Transcript intron_variant - - - - - - rs7311029 12:132406275 C CCDS9274.1 CCDS9274.1 Transcript downstream_gene_variant - - - - - - DISTANCE=369 rs7311029 12:132406275 C ENSESTG00000001551 ENSESTT00000003717 Transcript downstream_gene_variant - - - - - - DISTANCE=3058 rs7311029 12:132406275 C ENSESTG00000001787 ENSESTT00000004378 Transcript downstream_gene_variant - - - - - - DISTANCE=2787 rs4964914 12:132407175 G ENSESTG00000001551 ENSESTT00000003715 Transcript downstream_gene_variant - - - - - - DISTANCE=3958 rs4964914 12:132407175 G 8408 NM_003565.2 Transcript 3_prime_UTR_variant 4690 - - - - - rs4964914 12:132407175 G ENSESTG00000001578 ENSESTT00000003756 Transcript downstream_gene_variant - - - - - - DISTANCE=1032 rs4964914 12:132407175 G ENSESTG00000001578 ENSESTT00000003763 Transcript downstream_gene_variant - - - - - - DISTANCE=458 rs4964914 12:132407175 G ENSESTG00000001551 ENSESTT00000003723 Transcript intron_variant - - - - - - rs4964914 12:132407175 G CCDS9274.1 CCDS9274.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1269 rs4964914 12:132407175 G ENSESTG00000001551 ENSESTT00000003717 Transcript downstream_gene_variant - - - - - - DISTANCE=3958 rs4964914 12:132407175 G ENSESTG00000001787 ENSESTT00000004378 Transcript downstream_gene_variant - - - - - - DISTANCE=1887 rs7962505 12:132472719 C ENSESTG00000001616 ENSESTT00000003932 Transcript intron_variant - - - - - - rs7962505 12:132472719 C ENSESTG00000001616 ENSESTT00000003925 Transcript intron_variant - - - - - - rs7962505 12:132472719 C 57634 NM_015409.4 Transcript intron_variant - - - - - - rs7962505 12:132472719 C ENSESTG00000001616 ENSESTT00000003920 Transcript intron_variant - - - - - - rs7962505 12:132472719 C CCDS31929.2 CCDS31929.2 Transcript intron_variant - - - - - - rs1882311 12:133009844 G - - - intergenic_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084724 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084733 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084716 Transcript intron_variant - - - - - - rs7134338 12:133428466 A 55743 NM_001161346.1 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084753 Transcript upstream_gene_variant - - - - - - DISTANCE=3724 rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084746 Transcript upstream_gene_variant - - - - - - DISTANCE=3688 rs7134338 12:133428466 A CCDS53848.1 CCDS53848.1 Transcript intron_variant - - - - - - rs7134338 12:133428466 A CCDS53847.1 CCDS53847.1 Transcript intron_variant - - - - - - rs7134338 12:133428466 A 55743 NM_018223.2 Transcript intron_variant - - - - - - rs7134338 12:133428466 A 55743 NM_001161347.1 Transcript intron_variant - - - - - - rs7134338 12:133428466 A CCDS31937.1 CCDS31937.1 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084702 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084688 Transcript intron_variant - - - - - - rs7134338 12:133428466 A 55743 NM_001161345.1 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084691 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084680 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084684 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084713 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084741 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084737 Transcript intron_variant - - - - - - rs7134338 12:133428466 A 55743 NM_001161344.1 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084729 Transcript intron_variant - - - - - - rs7134338 12:133428466 A CCDS53849.1 CCDS53849.1 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084706 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084647 Transcript intron_variant - - - - - - rs7134338 12:133428466 A ENSESTG00000033463 ENSESTT00000084656 Transcript intron_variant - - - - - - rs7967091 12:133764292 C CCDS45012.1 CCDS45012.1 Transcript intron_variant - - - - - - rs7967091 12:133764292 C ENSESTG00000033428 ENSESTT00000084434 Transcript intron_variant - - - - - - rs7967091 12:133764292 C 10795 NM_001165882.2 Transcript intron_variant - - - - - - rs7967091 12:133764292 C ENSESTG00000033428 ENSESTT00000084431 Transcript intron_variant - - - - - - rs7967091 12:133764292 C 10795 NM_001165884.2 Transcript intron_variant - - - - - - rs7967091 12:133764292 C 10795 NM_001165887.1 Transcript intron_variant - - - - - - rs7967091 12:133764292 C CCDS53854.1 CCDS53854.1 Transcript intron_variant - - - - - - rs7967091 12:133764292 C 10795 NM_001165881.2 Transcript intron_variant - - - - - - rs7967091 12:133764292 C 10795 NM_001165885.1 Transcript intron_variant - - - - - - rs7967091 12:133764292 C CCDS53851.1 CCDS53851.1 Transcript intron_variant - - - - - - rs7967091 12:133764292 C CCDS53853.1 CCDS53853.1 Transcript intron_variant - - - - - - rs7967091 12:133764292 C 10795 NM_001165886.1 Transcript intron_variant - - - - - - rs7967091 12:133764292 C 10795 NM_003415.2 Transcript intron_variant - - - - - - rs7967091 12:133764292 C 10795 NM_152943.2 Transcript intron_variant - - - - - - rs7967091 12:133764292 C 10795 NM_001165883.1 Transcript intron_variant - - - - - - rs7967091 12:133764292 C CCDS53852.1 CCDS53852.1 Transcript intron_variant - - - - - - rs137919444 12:133785252 G CCDS45012.1 CCDS45012.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4136 rs137919444 12:133785252 G 10795 NM_001165885.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs137919444 12:133785252 G 10795 NM_001165882.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs137919444 12:133785252 G 10795 NM_001165881.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs137919444 12:133785252 G 10795 NM_003415.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs137919444 12:133785252 G 10795 NM_001165886.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs137919444 12:133785252 G 10795 NM_152943.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs137919444 12:133785252 G 10795 NM_001165884.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs137919444 12:133785252 G 10795 NM_001165887.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs137919444 12:133785252 G 10795 NM_001165883.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs149056164 12:133808638 G ENSESTG00000033436 ENSESTT00000084467 Transcript intron_variant - - - - - - rs149056164 12:133808638 G CCDS53855.1 CCDS53855.1 Transcript intron_variant - - - - - - rs149056164 12:133808638 G 647589 NM_001191054.1 Transcript intron_variant - - - - - - rs149056164 12:133808638 G ENSESTG00000033436 ENSESTT00000084470 Transcript intron_variant - - - - - - rs3963632 13:19021223 C - - - intergenic_variant - - - - - - rs9509379 13:19043558 C - - - intergenic_variant - - - - - - rs3963780 13:19186155 A - - - intergenic_variant - - - - - - rs7326150 13:19214913 T - - - intergenic_variant - - - - - - rs4037151 13:19302640 T - - - intergenic_variant - - - - - - rs4770761 13:19669539 G - - - intergenic_variant - - - - - - rs2446674 13:19875971 A 100101938 NR_027248.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs1411634 13:19897067 T 100101938 NR_027248.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs1856015 13:19912539 G 100101938 NR_027248.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs2492393 13:20030904 G 93492 NM_199254.2 Transcript intron_variant - - - - - - rs2492393 13:20030904 G 93492 NM_001141968.1 Transcript intron_variant - - - - - - rs2492393 13:20030904 G 93492 NM_130785.3 Transcript intron_variant - - - - - - rs2492393 13:20030904 G CCDS9285.1 CCDS9285.1 Transcript intron_variant - - - - - - rs2492393 13:20030904 G CCDS45013.1 CCDS45013.1 Transcript intron_variant - - - - - - rs2492393 13:20030904 G CCDS45014.1 CCDS45014.1 Transcript intron_variant - - - - - - rs2492393 13:20030904 G ENSESTG00000001852 ENSESTT00000004576 Transcript intron_variant - - - - - - rs1230949 13:20111133 A ENSESTG00000001847 ENSESTT00000004558 Transcript intron_variant - - - - - - rs1230949 13:20111133 A 93492 NM_199254.2 Transcript upstream_gene_variant - - - - - - DISTANCE=230 rs1230949 13:20111133 A 93492 NM_001141968.1 Transcript upstream_gene_variant - - - - - - DISTANCE=230 rs1230949 13:20111133 A 93492 NM_130785.3 Transcript upstream_gene_variant - - - - - - DISTANCE=230 rs9508843 13:20258009 C ENSESTG00000001831 ENSESTT00000004536 Transcript intron_variant - - - - - - rs9508843 13:20258009 C 55269 NR_003272.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs9508843 13:20258009 C ENSESTG00000001831 ENSESTT00000004542 Transcript intron_variant - - - - - - rs9508843 13:20258009 C 55269 NR_044998.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9508843 13:20258009 C ENSESTG00000001831 ENSESTT00000004546 Transcript intron_variant - - - - - - rs9506366 13:20314910 C 55269 NR_003272.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs9506366 13:20314910 C ENSESTG00000001831 ENSESTT00000004536 Transcript intron_variant - - - - - - rs9506366 13:20314910 C 55269 NR_044998.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9506366 13:20314910 C ENSESTG00000001831 ENSESTT00000004542 Transcript intron_variant - - - - - - rs9506366 13:20314910 C CCDS41870.1 CCDS41870.1 Transcript intron_variant - - - - - - rs9506366 13:20314910 C 55269 NM_001042414.2 Transcript intron_variant - - - - - - rs9506366 13:20314910 C ENSESTG00000001831 ENSESTT00000004517 Transcript intron_variant - - - - - - rs9506366 13:20314910 C ENSESTG00000001831 ENSESTT00000004546 Transcript intron_variant - - - - - - rs6490485 13:20344022 C 55269 NR_003272.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs6490485 13:20344022 C CCDS41870.1 CCDS41870.1 Transcript intron_variant - - - - - - rs6490485 13:20344022 C 55269 NR_044998.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6490485 13:20344022 C ENSESTG00000001822 ENSESTT00000004482 Transcript downstream_gene_variant - - - - - - DISTANCE=2446 rs6490485 13:20344022 C 55269 NM_001042414.2 Transcript intron_variant - - - - - - rs6490499 13:20552401 T 7750 NM_003453.3 Transcript intron_variant - - - - - - rs6490499 13:20552401 T 7750 NM_197968.2 Transcript intron_variant - - - - - - rs6490499 13:20552401 T ENSESTG00000001657 ENSESTT00000004071 Transcript intron_variant - - - - - - rs6490499 13:20552401 T ENSESTG00000001657 ENSESTT00000004054 Transcript intron_variant - - - - - - rs6490499 13:20552401 T 7750 NM_001190965.1 Transcript intron_variant - - - - - - rs6490499 13:20552401 T ENSESTG00000001657 ENSESTT00000004043 Transcript intron_variant - - - - - - rs6490499 13:20552401 T ENSESTG00000001657 ENSESTT00000004067 Transcript intron_variant - - - - - - rs6490499 13:20552401 T 7750 NM_001190964.1 Transcript intron_variant - - - - - - rs6490499 13:20552401 T ENSESTG00000001657 ENSESTT00000004019 Transcript intron_variant - - - - - - rs6490499 13:20552401 T ENSESTG00000001657 ENSESTT00000004028 Transcript intron_variant - - - - - - rs6490499 13:20552401 T ENSESTG00000001657 ENSESTT00000004057 Transcript intron_variant - - - - - - rs6490499 13:20552401 T ENSESTG00000001657 ENSESTT00000004031 Transcript intron_variant - - - - - - rs6490508 13:20590939 T CCDS45016.1 CCDS45016.1 Transcript intron_variant - - - - - - rs6490508 13:20590939 T 7750 NM_003453.3 Transcript intron_variant - - - - - - rs6490508 13:20590939 T ENSESTG00000001730 ENSESTT00000004277 Transcript intron_variant - - - - - - rs6490508 13:20590939 T 7750 NM_001190964.1 Transcript intron_variant - - - - - - rs6490508 13:20590939 T 7750 NM_197968.2 Transcript intron_variant - - - - - - rs6490508 13:20590939 T 7750 NM_001190965.1 Transcript intron_variant - - - - - - rs11147588 13:20757082 A 2706 NM_004004.5 Transcript downstream_gene_variant - - - - - - DISTANCE=4520 rs3002166 13:21172604 C 8100 NM_175605.3 Transcript intron_variant - - - - - - rs3002166 13:21172604 C CCDS31945.1 CCDS31945.1 Transcript intron_variant - - - - - - rs3002166 13:21172604 C ENSESTG00000016018 ENSESTT00000040409 Transcript intron_variant - - - - - - rs3002166 13:21172604 C ENSESTG00000016018 ENSESTT00000040399 Transcript downstream_gene_variant - - - - - - DISTANCE=2224 rs3002166 13:21172604 C ENSESTG00000016018 ENSESTT00000040383 Transcript intron_variant - - - - - - rs3002166 13:21172604 C ENSESTG00000016018 ENSESTT00000040412 Transcript intron_variant - - - - - - rs3002166 13:21172604 C CCDS31944.1 CCDS31944.1 Transcript intron_variant - - - - - - rs3002166 13:21172604 C 8100 NM_006531.3 Transcript intron_variant - - - - - - rs3002166 13:21172604 C ENSESTG00000016018 ENSESTT00000040198 Transcript downstream_gene_variant - - - - - - DISTANCE=2224 rs3002166 13:21172604 C ENSESTG00000016018 ENSESTT00000040393 Transcript intron_variant - - - - - - rs3002166 13:21172604 C ENSESTG00000016018 ENSESTT00000040420 Transcript upstream_gene_variant - - - - - - DISTANCE=1080 rs546154 13:21539066 C - - - intergenic_variant - - - - - - rs1200031 13:22161753 T ENSESTG00000017169 ENSESTT00000043225 Transcript intron_variant - - - - - - rs1200031 13:22161753 T 221154 NM_152726.2 Transcript intron_variant - - - - - - rs1200031 13:22161753 T ENSESTG00000017169 ENSESTT00000043197 Transcript intron_variant - - - - - - rs1200031 13:22161753 T CCDS9297.1 CCDS9297.1 Transcript intron_variant - - - - - - rs1886168 13:22170284 A ENSESTG00000017169 ENSESTT00000043225 Transcript intron_variant - - - - - - rs1886168 13:22170284 A 221154 NM_152726.2 Transcript intron_variant - - - - - - rs1886168 13:22170284 A ENSESTG00000017169 ENSESTT00000043197 Transcript intron_variant - - - - - - rs1886168 13:22170284 A CCDS9297.1 CCDS9297.1 Transcript intron_variant - - - - - - rs1886169 13:22185185 G ENSESTG00000017138 ENSESTT00000043045 Transcript upstream_gene_variant - - - - - - DISTANCE=4070 rs1886169 13:22185185 G ENSESTG00000017169 ENSESTT00000043197 Transcript intron_variant - - - - - - rs9316485 13:22188452 C - ENSR00001507725 RegulatoryFeature regulatory_region_variant - - - - - - rs9316485 13:22188452 C ENSESTG00000017138 ENSESTT00000043045 Transcript upstream_gene_variant - - - - - - DISTANCE=803 rs9316485 13:22188452 C ENSESTG00000017169 ENSESTT00000043197 Transcript intron_variant - - - - - - rs2874240 13:22235228 T ENSESTG00000017169 ENSESTT00000043197 Transcript intron_variant - - - - - - rs667219 13:22329088 A - - - intergenic_variant - - - - - - rs547717 13:22355407 A - - - intergenic_variant - - - - - - rs9507016 13:23656612 A - - - intergenic_variant - - - - - - rs794493 13:23784971 T CCDS9299.1 CCDS9299.1 Transcript intron_variant - - - - - - rs794493 13:23784971 T ENSESTG00000020608 ENSESTT00000051813 Transcript intron_variant - - - - - - rs794493 13:23784971 T 6445 NM_000231.2 Transcript intron_variant - - - - - - rs794493 13:23784971 T ENSESTG00000020608 ENSESTT00000051791 Transcript intron_variant - - - - - - rs2765090 13:24491930 A 400110 XM_003846335.1 Transcript intron_variant - - - - - - rs9670805 13:24504074 A 400110 XM_003846335.1 Transcript intron_variant - - - - - - rs2793489 13:24822925 A ENSESTG00000009492 ENSESTT00000023784 Transcript upstream_gene_variant - - - - - - DISTANCE=2907 rs2793489 13:24822925 A CCDS53857.1 CCDS53857.1 Transcript intron_variant - - - - - - rs2793489 13:24822925 A ENSESTG00000033156 ENSESTT00000083781 Transcript intron_variant - - - - - - rs2793489 13:24822925 A CCDS9305.1 CCDS9305.1 Transcript upstream_gene_variant - - - - - - DISTANCE=912 rs2793489 13:24822925 A ENSESTG00000033156 ENSESTT00000083786 Transcript intron_variant - - - - - - rs2793489 13:24822925 A 221178 NM_153023.2 Transcript intron_variant - - - - - - rs2793489 13:24822925 A 221178 NM_001166271.1 Transcript intron_variant - - - - - - rs2793489 13:24822925 A 100874231 NR_046531.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3962 rs4288857 13:24878200 A ENSESTG00000009492 ENSESTT00000023832 Transcript downstream_gene_variant - - - - - - DISTANCE=751 rs4288857 13:24878200 A ENSESTG00000009492 ENSESTT00000023812 Transcript downstream_gene_variant - - - - - - DISTANCE=751 rs4288857 13:24878200 A ENSESTG00000009492 ENSESTT00000023834 Transcript downstream_gene_variant - - - - - - DISTANCE=2647 rs4288857 13:24878200 A CCDS53857.1 CCDS53857.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1289 rs4288857 13:24878200 A CCDS9305.1 CCDS9305.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1289 rs4288857 13:24878200 A 221178 NM_153023.2 Transcript 3_prime_UTR_variant 3681 - - - - - rs4288857 13:24878200 A ENSESTG00000009492 ENSESTT00000023840 Transcript downstream_gene_variant - - - - - - DISTANCE=751 rs4288857 13:24878200 A 221178 NM_001166271.1 Transcript 3_prime_UTR_variant 5445 - - - - - rs4288857 13:24878200 A ENSESTG00000009492 ENSESTT00000023821 Transcript downstream_gene_variant - - - - - - DISTANCE=2647 rs4288857 13:24878200 A ENSESTG00000009515 ENSESTT00000023864 Transcript upstream_gene_variant - - - - - - DISTANCE=3104 rs4288857 13:24878200 A ENSESTG00000009492 ENSESTT00000023846 Transcript downstream_gene_variant - - - - - - DISTANCE=2647 rs2862238 13:24899808 A 338872 NM_178540.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3139 rs2862238 13:24899808 A ENSESTG00000009515 ENSESTT00000023866 Transcript downstream_gene_variant - - - - - - DISTANCE=4197 rs2862238 13:24899808 A ENSESTG00000009515 ENSESTT00000023864 Transcript downstream_gene_variant - - - - - - DISTANCE=4129 rs2862238 13:24899808 A CCDS9306.1 CCDS9306.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3902 rs2119495 13:25093219 G - - - intergenic_variant - - - - - - rs6490976 13:25299179 C - - - intergenic_variant - - - - - - rs7327399 13:25454258 G ENSESTG00000009606 ENSESTT00000024128 Transcript downstream_gene_variant - - - - - - DISTANCE=202 rs7327399 13:25454258 G ENSESTG00000009606 ENSESTT00000024113 Transcript downstream_gene_variant - - - - - - DISTANCE=202 rs7327399 13:25454258 G ENSESTG00000009606 ENSESTT00000024118 Transcript downstream_gene_variant - - - - - - DISTANCE=202 rs7327399 13:25454258 G CCDS9308.2 CCDS9308.2 Transcript downstream_gene_variant - - - - - - DISTANCE=835 rs7327399 13:25454258 G ENSESTG00000009652 ENSESTT00000024209 Transcript downstream_gene_variant - - - - - - DISTANCE=3106 rs7327399 13:25454258 G ENSESTG00000009606 ENSESTT00000024121 Transcript downstream_gene_variant - - - - - - DISTANCE=202 rs7327399 13:25454258 G 55835 NR_047595.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2154 rs7327399 13:25454258 G 55835 NM_018451.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2154 rs7327399 13:25454258 G CCDS9310.1 CCDS9310.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3057 rs7327399 13:25454258 G 55835 NR_047594.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2154 rs7327399 13:25454258 G 56163 NM_001184993.1 Transcript downstream_gene_variant - - - - - - DISTANCE=199 rs7327399 13:25454258 G 56163 NM_031277.2 Transcript downstream_gene_variant - - - - - - DISTANCE=199 rs3002253 13:25620838 T - - - intergenic_variant - - - - - - rs2994872 13:25654073 G - - - intergenic_variant - - - - - - rs7985952 13:26074591 C CCDS41873.1 CCDS41873.1 Transcript intron_variant - - - - - - rs7985952 13:26074591 C ENSESTG00000032068 ENSESTT00000080997 Transcript intron_variant - - - - - - rs7985952 13:26074591 C ENSESTG00000032068 ENSESTT00000081040 Transcript intron_variant - - - - - - rs7985952 13:26074591 C ENSESTG00000032068 ENSESTT00000081046 Transcript intron_variant - - - - - - rs7985952 13:26074591 C 51761 NM_016529.4 Transcript intron_variant - - - - - - rs7985952 13:26074591 C ENSESTG00000032068 ENSESTT00000081007 Transcript intron_variant - - - - - - rs7985952 13:26074591 C ENSESTG00000032068 ENSESTT00000081057 Transcript intron_variant - - - - - - rs7985952 13:26074591 C ENSESTG00000032068 ENSESTT00000081061 Transcript intron_variant - - - - - - rs7985952 13:26074591 C ENSESTG00000032068 ENSESTT00000081051 Transcript intron_variant - - - - - - rs1182000 13:26480090 T ENSESTG00000032152 ENSESTT00000081233 Transcript intron_variant - - - - - - rs1182000 13:26480090 T CCDS41873.1 CCDS41873.1 Transcript intron_variant - - - - - - rs1182000 13:26480090 T 51761 NM_016529.4 Transcript intron_variant - - - - - - rs1182000 13:26480090 T ENSESTG00000032152 ENSESTT00000081215 Transcript intron_variant - - - - - - rs306405 13:26511482 T ENSESTG00000032152 ENSESTT00000081233 Transcript intron_variant - - - - - - rs306405 13:26511482 T CCDS41873.1 CCDS41873.1 Transcript intron_variant - - - - - - rs306405 13:26511482 T 51761 NM_016529.4 Transcript intron_variant - - - - - - rs306405 13:26511482 T ENSESTG00000032152 ENSESTT00000081215 Transcript intron_variant - - - - - - rs515058 13:27129697 C - ENSR00001508035 RegulatoryFeature regulatory_region_variant - - - - - - rs515058 13:27129697 C ENSESTG00000019180 ENSESTT00000048434 Transcript upstream_gene_variant - - - - - - DISTANCE=2770 rs515058 13:27129697 C ENSESTG00000019180 ENSESTT00000048392 Transcript upstream_gene_variant - - - - - - DISTANCE=2136 rs515058 13:27129697 C ENSESTG00000019180 ENSESTT00000048424 Transcript upstream_gene_variant - - - - - - DISTANCE=2221 rs515058 13:27129697 C 10810 NM_006646.5 Transcript upstream_gene_variant - - - - - - DISTANCE=2143 rs515058 13:27129697 C ENSESTG00000019180 ENSESTT00000048413 Transcript upstream_gene_variant - - - - - - DISTANCE=2136 rs485764 13:27185761 A ENSESTG00000019180 ENSESTT00000048434 Transcript intron_variant - - - - - - rs485764 13:27185761 A ENSESTG00000019180 ENSESTT00000048392 Transcript intron_variant - - - - - - rs485764 13:27185761 A ENSESTG00000019180 ENSESTT00000048424 Transcript intron_variant - - - - - - rs485764 13:27185761 A 10810 NM_006646.5 Transcript intron_variant - - - - - - rs485764 13:27185761 A ENSESTG00000019180 ENSESTT00000048413 Transcript intron_variant - - - - - - rs2182930 13:27531378 T - ENSR00000513286 RegulatoryFeature regulatory_region_variant - - - - - - rs2182930 13:27531378 T - - - intergenic_variant - - - - - - rs1547678 13:27553977 G ENSESTG00000019372 ENSESTT00000048682 Transcript intron_variant - - - - - - rs1535643 13:28062954 A 100873768 NR_046934.1 Transcript downstream_gene_variant - - - - - - DISTANCE=585 rs4771131 13:28064303 G 100873768 NR_046934.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1934 rs7990845 13:28071035 G - - - intergenic_variant - - - - - - rs1228363 13:28076869 G - - - intergenic_variant - - - - - - rs1218884 13:28099242 G - - - intergenic_variant - - - - - - rs2181429 13:28269701 T - - - intergenic_variant - - - - - - rs9512818 13:28285189 A - - - intergenic_variant - - - - - - rs1778810 13:28287563 A - - - intergenic_variant - - - - - - rs1230998 13:28302277 C - - - intergenic_variant - - - - - - rs9554209 13:28527623 C - - - intergenic_variant - - - - - - rs2504227 13:28593541 G CCDS31953.1 CCDS31953.1 Transcript intron_variant - - - - - - rs2504227 13:28593541 G ENSESTG00000015282 ENSESTT00000038280 Transcript upstream_gene_variant - - - - - - DISTANCE=4880 rs2504227 13:28593541 G ENSESTG00000015282 ENSESTT00000038284 Transcript upstream_gene_variant - - - - - - DISTANCE=4928 rs2504227 13:28593541 G 2322 NM_004119.2 Transcript intron_variant - - - - - - rs4771226 13:28747406 A ENSESTG00000015242 ENSESTT00000038182 Transcript intron_variant - - - - - - rs4771226 13:28747406 A CCDS9329.2 CCDS9329.2 Transcript intron_variant - - - - - - rs4771226 13:28747406 A 255967 NM_175854.7 Transcript intron_variant - - - - - - rs7983129 13:29173784 C - - - intergenic_variant - - - - - - rs1161121 13:29209611 C - - - intergenic_variant - - - - - - rs947027 13:29275102 C 283537 NM_001135919.1 Transcript intron_variant - - - - - - rs947027 13:29275102 C 100873762 NR_046928.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2737 rs947027 13:29275102 C CCDS9332.1 CCDS9332.1 Transcript downstream_gene_variant - - - - - - DISTANCE=532 rs947027 13:29275102 C ENSESTG00000010279 ENSESTT00000025711 Transcript downstream_gene_variant - - - - - - DISTANCE=252 rs947027 13:29275102 C 283537 NM_181785.3 Transcript 3_prime_UTR_variant 2460 - - - - - rs947027 13:29275102 C CCDS45021.1 CCDS45021.1 Transcript intron_variant - - - - - - rs947027 13:29275102 C ENSESTG00000010279 ENSESTT00000025710 Transcript downstream_gene_variant - - - - - - DISTANCE=252 rs1300235 13:29291886 G 283537 NM_001135919.1 Transcript intron_variant - - - - - - rs1300235 13:29291886 G CCDS9332.1 CCDS9332.1 Transcript intron_variant - - - - - - rs1300235 13:29291886 G 283537 NM_181785.3 Transcript intron_variant - - - - - - rs1300235 13:29291886 G CCDS45021.1 CCDS45021.1 Transcript intron_variant - - - - - - rs1300235 13:29291886 G ENSESTG00000010279 ENSESTT00000025710 Transcript upstream_gene_variant - - - - - - DISTANCE=4754 rs1161292 13:29321313 A - - - intergenic_variant - - - - - - rs1772325 13:29366636 G - - - intergenic_variant - - - - - - rs2496116 13:29447018 A ENSESTG00000010268 ENSESTT00000025679 Transcript intron_variant - - - - - - rs2453705 13:29455224 A ENSESTG00000010268 ENSESTT00000025679 Transcript intron_variant - - - - - - rs3926786 13:29573525 G ENSESTG00000010268 ENSESTT00000025679 Transcript intron_variant - - - - - - rs226907 13:29592826 G ENSESTG00000010268 ENSESTT00000025679 Transcript intron_variant - - - - - - rs2475521 13:29650487 G CCDS45022.1 CCDS45022.1 Transcript intron_variant - - - - - - rs2475521 13:29650487 G ENSESTG00000010274 ENSESTT00000025685 Transcript intron_variant - - - - - - rs2475521 13:29650487 G 23281 NM_001033602.2 Transcript intron_variant - - - - - - rs9506104 13:29675708 C CCDS45022.1 CCDS45022.1 Transcript intron_variant - - - - - - rs9506104 13:29675708 C ENSESTG00000010274 ENSESTT00000025685 Transcript intron_variant - - - - - - rs9506104 13:29675708 C 23281 NM_001033602.2 Transcript intron_variant - - - - - - rs4769682 13:29712341 A CCDS45022.1 CCDS45022.1 Transcript intron_variant - - - - - - rs4769682 13:29712341 A ENSESTG00000010274 ENSESTT00000025685 Transcript intron_variant - - - - - - rs4769682 13:29712341 A 23281 NM_001033602.2 Transcript intron_variant - - - - - - rs7999914 13:29723985 T CCDS45022.1 CCDS45022.1 Transcript intron_variant - - - - - - rs7999914 13:29723985 T ENSESTG00000010274 ENSESTT00000025685 Transcript intron_variant - - - - - - rs7999914 13:29723985 T 23281 NM_001033602.2 Transcript intron_variant - - - - - - rs4769683 13:29728794 C CCDS45022.1 CCDS45022.1 Transcript intron_variant - - - - - - rs4769683 13:29728794 C ENSESTG00000010274 ENSESTT00000025685 Transcript intron_variant - - - - - - rs4769683 13:29728794 C 23281 NM_001033602.2 Transcript intron_variant - - - - - - rs3011463 13:29730114 C CCDS45022.1 CCDS45022.1 Transcript intron_variant - - - - - - rs3011463 13:29730114 C ENSESTG00000010274 ENSESTT00000025685 Transcript intron_variant - - - - - - rs3011463 13:29730114 C 23281 NM_001033602.2 Transcript intron_variant - - - - - - rs2987337 13:29742513 A CCDS45022.1 CCDS45022.1 Transcript intron_variant - - - - - - rs2987337 13:29742513 A ENSESTG00000010274 ENSESTT00000025685 Transcript intron_variant - - - - - - rs2987337 13:29742513 A 23281 NM_001033602.2 Transcript intron_variant - - - - - - rs9508359 13:29903316 C CCDS45022.1 CCDS45022.1 Transcript intron_variant - - - - - - rs9508359 13:29903316 C 23281 NM_001033602.2 Transcript intron_variant - - - - - - rs582496 13:30173142 C ENSESTG00000025480 ENSESTT00000064285 Transcript upstream_gene_variant - - - - - - DISTANCE=2877 rs582496 13:30173142 C ENSESTG00000025480 ENSESTT00000064297 Transcript upstream_gene_variant - - - - - - DISTANCE=3645 rs582496 13:30173142 C 6541 NM_003045.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3317 rs582496 13:30173142 C ENSESTG00000025480 ENSESTT00000064291 Transcript upstream_gene_variant - - - - - - DISTANCE=3322 rs7993598 13:30224420 T - - - intergenic_variant - - - - - - rs7993599 13:30224422 T - - - intergenic_variant - - - - - - rs7332567 13:30939373 T - ENSR00000513718 RegulatoryFeature regulatory_region_variant - - - - - - rs7332567 13:30939373 T ENSESTG00000010823 ENSESTT00000027098 Transcript upstream_gene_variant - - - - - - DISTANCE=1141 rs7332567 13:30939373 T 100188949 NR_024464.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2388539 13:30963100 C - ENSR00000513723 RegulatoryFeature regulatory_region_variant - - - - - - rs2388539 13:30963100 C - - - intergenic_variant - - - - - - rs9285075 13:31317423 G - ENSR00000150935 RegulatoryFeature regulatory_region_variant - - - - - - rs9285075 13:31317423 G 241 NM_001629.3 Transcript intron_variant - - - - - - rs9285075 13:31317423 G 241 NM_001204406.1 Transcript intron_variant - - - - - - rs9285075 13:31317423 G ENSESTG00000010696 ENSESTT00000026821 Transcript intron_variant - - - - - - rs9285075 13:31317423 G CCDS9337.1 CCDS9337.1 Transcript intron_variant - - - - - - rs9285075 13:31317423 G ENSESTG00000010696 ENSESTT00000026813 Transcript intron_variant - - - - - - rs1849165 13:31863388 C ENSESTG00000024329 ENSESTT00000061669 Transcript intron_variant - - - - - - rs1849165 13:31863388 C ENSESTG00000024329 ENSESTT00000061640 Transcript downstream_gene_variant - - - - - - DISTANCE=4500 rs1849165 13:31863388 C 145173 NM_194318.3 Transcript intron_variant - - - - - - rs1849165 13:31863388 C CCDS9341.1 CCDS9341.1 Transcript intron_variant - - - - - - rs4941812 13:31875509 T ENSESTG00000024329 ENSESTT00000061669 Transcript intron_variant - - - - - - rs4941812 13:31875509 T 145173 NM_194318.3 Transcript intron_variant - - - - - - rs4941812 13:31875509 T CCDS9341.1 CCDS9341.1 Transcript intron_variant - - - - - - rs1744793 13:32189672 C - - - intergenic_variant - - - - - - rs277132 13:32212063 T - - - intergenic_variant - - - - - - rs4943620 13:32242519 A - - - intergenic_variant - - - - - - rs810195 13:32505927 T 196549 NR_027062.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs810195 13:32505927 T ENSESTG00000024708 ENSESTT00000062442 Transcript intron_variant - - - - - - rs810195 13:32505927 T ENSESTG00000024538 ENSESTT00000062046 Transcript intron_variant - - - - - - rs397927 13:32629695 G ENSESTG00000024576 ENSESTT00000062140 Transcript intron_variant - - - - - - rs397927 13:32629695 G 10129 NM_023037.2 Transcript intron_variant - - - - - - rs397927 13:32629695 G CCDS41875.1 CCDS41875.1 Transcript intron_variant - - - - - - rs397927 13:32629695 G ENSESTG00000024576 ENSESTT00000062098 Transcript intron_variant - - - - - - rs481686 13:33480144 G 100874167 NR_047020.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4147235 13:33888818 G 90627 NM_001243476.1 Transcript intron_variant - - - - - - rs7983609 13:34322411 C - - - intergenic_variant - - - - - - rs4941763 13:34323386 A - - - intergenic_variant - - - - - - rs7335464 13:34340781 T - - - intergenic_variant - - - - - - rs1041091 13:34404287 A CCDS45025.1 CCDS45025.1 Transcript intron_variant - - - - - - rs1041091 13:34404287 A 5983 NM_002915.3 Transcript intron_variant - - - - - - rs1041091 13:34404287 A CCDS9352.1 CCDS9352.1 Transcript intron_variant - - - - - - rs1041091 13:34404287 A ENSESTG00000017540 ENSESTT00000044175 Transcript intron_variant - - - - - - rs1041091 13:34404287 A 5983 NM_181558.2 Transcript intron_variant - - - - - - rs1041091 13:34404287 A ENSESTG00000017540 ENSESTT00000044220 Transcript intron_variant - - - - - - rs7329155 13:34744812 G - - - intergenic_variant - - - - - - rs4482149 13:34995154 C - ENSR00001508648 RegulatoryFeature regulatory_region_variant - - - - - - rs4482149 13:34995154 C - - - intergenic_variant - - - - - - rs4943223 13:35144047 G 100874179 NR_047036.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4943223 13:35144047 G ENSESTG00000007319 ENSESTT00000018443 Transcript intron_variant - - - - - - rs4943223 13:35144047 G ENSESTG00000007315 ENSESTT00000018427 Transcript intron_variant - - - - - - rs2183208 13:35172622 G 100874179 NR_047036.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2183208 13:35172622 G ENSESTG00000007319 ENSESTT00000018443 Transcript intron_variant - - - - - - rs2183208 13:35172622 G ENSESTG00000007315 ENSESTT00000018427 Transcript intron_variant - - - - - - rs9541337 13:35177385 C 100874179 NR_047036.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9541337 13:35177385 C ENSESTG00000007319 ENSESTT00000018443 Transcript intron_variant - - - - - - rs9541337 13:35177385 C ENSESTG00000007315 ENSESTT00000018427 Transcript intron_variant - - - - - - rs1041303 13:35192969 G ENSESTG00000007262 ENSESTT00000018311 Transcript downstream_gene_variant - - - - - - DISTANCE=2540 rs1041303 13:35192969 G 100874179 NR_047036.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1041303 13:35192969 G ENSESTG00000007319 ENSESTT00000018443 Transcript intron_variant - - - - - - rs1041303 13:35192969 G ENSESTG00000007315 ENSESTT00000018427 Transcript intron_variant - - - - - - rs4943245 13:35279887 C ENSESTG00000007315 ENSESTT00000018427 Transcript intron_variant - - - - - - rs1605646 13:35294918 A ENSESTG00000007315 ENSESTT00000018427 Transcript intron_variant - - - - - - rs9541980 13:35297805 C ENSESTG00000007315 ENSESTT00000018427 Transcript intron_variant - - - - - - rs4095093 13:35299941 A ENSESTG00000007315 ENSESTT00000018427 Transcript intron_variant - - - - - - rs7981708 13:35331832 C ENSESTG00000007315 ENSESTT00000018427 Transcript intron_variant - - - - - - rs2322524 13:35791005 T 26960 NM_015678.4 Transcript intron_variant - - - - - - rs2322524 13:35791005 T CCDS45026.1 CCDS45026.1 Transcript intron_variant - - - - - - rs7326557 13:35975311 G 26960 NM_015678.4 Transcript intron_variant - - - - - - rs7326557 13:35975311 G CCDS45026.1 CCDS45026.1 Transcript intron_variant - - - - - - rs1171053 13:36498940 G ENSESTG00000006549 ENSESTT00000016501 Transcript intron_variant - - - - - - rs1171053 13:36498940 G 9201 NM_004734.4 Transcript intron_variant - - - - - - rs1171053 13:36498940 G CCDS9354.1 CCDS9354.1 Transcript intron_variant - - - - - - rs1171053 13:36498940 G ENSESTG00000006549 ENSESTT00000016505 Transcript intron_variant - - - - - - rs1418988 13:36515160 T ENSESTG00000006549 ENSESTT00000016501 Transcript intron_variant - - - - - - rs1418988 13:36515160 T 9201 NM_004734.4 Transcript intron_variant - - - - - - rs1418988 13:36515160 T CCDS9354.1 CCDS9354.1 Transcript intron_variant - - - - - - rs1418988 13:36515160 T ENSESTG00000006549 ENSESTT00000016505 Transcript intron_variant - - - - - - rs4245375 13:36551994 T ENSESTG00000006549 ENSESTT00000016501 Transcript intron_variant - - - - - - rs4245375 13:36551994 T 9201 NM_004734.4 Transcript intron_variant - - - - - - rs4245375 13:36551994 T CCDS9354.1 CCDS9354.1 Transcript intron_variant - - - - - - rs1170995 13:36581207 G ENSESTG00000006549 ENSESTT00000016501 Transcript intron_variant - - - - - - rs1170995 13:36581207 G 9201 NM_004734.4 Transcript intron_variant - - - - - - rs1170995 13:36581207 G CCDS9354.1 CCDS9354.1 Transcript intron_variant - - - - - - rs1410640 13:36715371 C - - - intergenic_variant - - - - - - rs978748 13:36820751 C CCDS45028.1 CCDS45028.1 Transcript intron_variant - - - - - - rs978748 13:36820751 C ENSESTG00000025553 ENSESTT00000064532 Transcript intron_variant - - - - - - rs978748 13:36820751 C CCDS53863.1 CCDS53863.1 Transcript intron_variant - - - - - - rs978748 13:36820751 C CCDS55896.1 CCDS55896.1 Transcript intron_variant - - - - - - rs978748 13:36820751 C 728591 NM_001144982.2 Transcript intron_variant - - - - - - rs978748 13:36820751 C 728591 NM_001144983.2 Transcript intron_variant - - - - - - rs978748 13:36820751 C CCDS55897.1 CCDS55897.1 Transcript intron_variant - - - - - - rs978748 13:36820751 C ENSESTG00000025553 ENSESTT00000064590 Transcript intron_variant - - - - - - rs978748 13:36820751 C 728591 NM_001144986.2 Transcript intron_variant - - - - - - rs978748 13:36820751 C CCDS45029.1 CCDS45029.1 Transcript intron_variant - - - - - - rs978748 13:36820751 C 728591 NM_001198908.1 Transcript intron_variant - - - - - - rs978748 13:36820751 C 728591 NM_001144985.2 Transcript intron_variant - - - - - - rs978748 13:36820751 C ENSESTG00000025553 ENSESTT00000064479 Transcript intron_variant - - - - - - rs978748 13:36820751 C 728591 NM_001144981.2 Transcript intron_variant - - - - - - rs978748 13:36820751 C CCDS45027.1 CCDS45027.1 Transcript intron_variant - - - - - - rs978748 13:36820751 C 728591 NM_001144984.2 Transcript intron_variant - - - - - - rs978748 13:36820751 C 100526761 NM_001198910.1 Transcript intron_variant - - - - - - rs1341482 13:36899409 G 23111 NM_001142294.1 Transcript intron_variant - - - - - - rs1341482 13:36899409 G 23111 NM_001142295.1 Transcript intron_variant - - - - - - rs1341482 13:36899409 G 23111 NM_001142296.1 Transcript intron_variant - - - - - - rs1341482 13:36899409 G 23111 NM_015087.4 Transcript intron_variant - - - - - - rs1341482 13:36899409 G ENSESTG00000025514 ENSESTT00000064412 Transcript intron_variant - - - - - - rs1341482 13:36899409 G ENSESTG00000025469 ENSESTT00000064323 Transcript intron_variant - - - - - - rs1341482 13:36899409 G CCDS9356.1 CCDS9356.1 Transcript intron_variant - - - - - - rs1341484 13:36920147 G - ENSR00000150983 RegulatoryFeature regulatory_region_variant - - - - - - rs1341484 13:36920147 G 23111 NM_001142294.1 Transcript intron_variant - - - - - - rs1341484 13:36920147 G 23111 NM_001142295.1 Transcript intron_variant - - - - - - rs1341484 13:36920147 G ENSESTG00000024801 ENSESTT00000062668 Transcript upstream_gene_variant - - - - - - DISTANCE=422 rs1341484 13:36920147 G 100507135 NR_045180.1 Transcript upstream_gene_variant - - - - - - DISTANCE=421 rs1341484 13:36920147 G ENSESTG00000025469 ENSESTT00000064311 Transcript intron_variant - - - - - - rs1341484 13:36920147 G 23111 NM_015087.4 Transcript intron_variant - - - - - - rs1341484 13:36920147 G ENSESTG00000025469 ENSESTT00000064323 Transcript intron_variant - - - - - - rs1341484 13:36920147 G ENSESTG00000025469 ENSESTT00000064255 Transcript intron_variant - - - - - - rs1341484 13:36920147 G ENSESTG00000024801 ENSESTT00000062658 Transcript upstream_gene_variant - - - - - - DISTANCE=421 rs1341484 13:36920147 G 23111 NM_001142296.1 Transcript intron_variant - - - - - - rs1341484 13:36920147 G ENSESTG00000024801 ENSESTT00000062698 Transcript upstream_gene_variant - - - - - - DISTANCE=436 rs1341484 13:36920147 G 100507135 NR_045181.1 Transcript upstream_gene_variant - - - - - - DISTANCE=421 rs1341484 13:36920147 G ENSESTG00000025469 ENSESTT00000064232 Transcript intron_variant - - - - - - rs1341484 13:36920147 G ENSESTG00000025469 ENSESTT00000064276 Transcript intron_variant - - - - - - rs4941834 13:36921840 A 23111 NM_001142294.1 Transcript intron_variant - - - - - - rs4941834 13:36921840 A 23111 NM_001142295.1 Transcript upstream_gene_variant - - - - - - DISTANCE=906 rs4941834 13:36921840 A ENSESTG00000024801 ENSESTT00000062668 Transcript intron_variant - - - - - - rs4941834 13:36921840 A 100507135 NR_045180.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4941834 13:36921840 A ENSESTG00000025469 ENSESTT00000064311 Transcript upstream_gene_variant - - - - - - DISTANCE=987 rs4941834 13:36921840 A 23111 NM_015087.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1194 rs4941834 13:36921840 A ENSESTG00000025469 ENSESTT00000064323 Transcript upstream_gene_variant - - - - - - DISTANCE=1451 rs4941834 13:36921840 A ENSESTG00000025469 ENSESTT00000064255 Transcript intron_variant - - - - - - rs4941834 13:36921840 A ENSESTG00000024801 ENSESTT00000062658 Transcript intron_variant - - - - - - rs4941834 13:36921840 A 23111 NM_001142296.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1194 rs4941834 13:36921840 A ENSESTG00000024801 ENSESTT00000062698 Transcript intron_variant - - - - - - rs4941834 13:36921840 A 100507135 NR_045181.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4941834 13:36921840 A ENSESTG00000025469 ENSESTT00000064232 Transcript intron_variant - - - - - - rs4941834 13:36921840 A ENSESTG00000025469 ENSESTT00000064276 Transcript upstream_gene_variant - - - - - - DISTANCE=936 rs4306383 13:36952773 A - - - intergenic_variant - - - - - - rs7490320 13:37037566 T - - - intergenic_variant - - - - - - rs1927560 13:37057488 G - - - intergenic_variant - - - - - - rs6563482 13:37067191 A - - - intergenic_variant - - - - - - rs4525364 13:37068698 G - - - intergenic_variant - - - - - - rs7993542 13:37141582 C - - - intergenic_variant - - - - - - rs978381 13:37151944 G - - - intergenic_variant - - - - - - rs686301 13:37245403 G ENSESTG00000024910 ENSESTT00000062916 Transcript upstream_gene_variant - - - - - - DISTANCE=2646 rs686301 13:37245403 G 400120 NM_203451.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2646 rs3904080 13:37373685 T - - - intergenic_variant - - - - - - rs516094 13:37439018 T 4093 NM_001127217.2 Transcript intron_variant - - - - - - rs516094 13:37439018 T ENSESTG00000025416 ENSESTT00000064206 Transcript intron_variant - - - - - - rs516094 13:37439018 T ENSESTG00000025416 ENSESTT00000064170 Transcript intron_variant - - - - - - rs516094 13:37439018 T CCDS45032.1 CCDS45032.1 Transcript intron_variant - - - - - - rs516094 13:37439018 T 4093 NM_005905.5 Transcript intron_variant - - - - - - rs516094 13:37439018 T CCDS9360.1 CCDS9360.1 Transcript intron_variant - - - - - - rs9315505 13:38174238 A 10631 NM_001135934.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1257 rs9315505 13:38174238 A ENSESTG00000016640 ENSESTT00000041781 Transcript upstream_gene_variant - - - - - - DISTANCE=1538 rs9315505 13:38174238 A 10631 NM_001135936.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1257 rs9315505 13:38174238 A CCDS53864.1 CCDS53864.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1375 rs9315505 13:38174238 A ENSESTG00000016640 ENSESTT00000041765 Transcript upstream_gene_variant - - - - - - DISTANCE=1257 rs9315505 13:38174238 A ENSESTG00000016640 ENSESTT00000041770 Transcript upstream_gene_variant - - - - - - DISTANCE=1257 rs9315505 13:38174238 A CCDS45034.1 CCDS45034.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1375 rs9315505 13:38174238 A ENSESTG00000016640 ENSESTT00000041784 Transcript upstream_gene_variant - - - - - - DISTANCE=1538 rs9315505 13:38174238 A 10631 NM_001135935.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1257 rs9315505 13:38174238 A 10631 NM_006475.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1257 rs9315505 13:38174238 A CCDS9364.1 CCDS9364.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1375 rs1570611 13:38240294 C CCDS45037.1 CCDS45037.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C 7223 NM_003306.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C CCDS45038.1 CCDS45038.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C CCDS45039.1 CCDS45039.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C 7223 NM_001135958.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C CCDS9365.1 CCDS9365.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C 7223 NM_001135956.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C CCDS45035.1 CCDS45035.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C 7223 NM_016179.2 Transcript intron_variant - - - - - - rs1570611 13:38240294 C CCDS45036.1 CCDS45036.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C 7223 NM_001135955.1 Transcript intron_variant - - - - - - rs1570611 13:38240294 C 7223 NM_001135957.1 Transcript intron_variant - - - - - - rs669491 13:38748211 G - - - intergenic_variant - - - - - - rs676253 13:38831204 C - - - intergenic_variant - - - - - - rs2442342 13:39238107 T - - - intergenic_variant - - - - - - rs2442377 13:39248329 C - - - intergenic_variant - - - - - - rs2496423 13:39263714 C CCDS31960.1 CCDS31960.1 Transcript missense_variant 2233 2233 745 S/P Tcc/Ccc - PolyPhen=benign;SIFT=tolerated rs2496423 13:39263714 C 341640 NM_207361.4 Transcript missense_variant 2542 2233 745 S/P Tcc/Ccc - PolyPhen=benign;SIFT=tolerated rs2496427 13:39266862 C CCDS31960.1 CCDS31960.1 Transcript intron_variant - - - - - - rs2496427 13:39266862 C 341640 NM_207361.4 Transcript intron_variant - - - - - - rs2496429 13:39270259 C CCDS31960.1 CCDS31960.1 Transcript intron_variant - - - - - - rs2496429 13:39270259 C 341640 NM_207361.4 Transcript intron_variant - - - - - - rs2442369 13:39283454 G CCDS31960.1 CCDS31960.1 Transcript intron_variant - - - - - - rs2442369 13:39283454 G 341640 NM_207361.4 Transcript intron_variant - - - - - - rs2442355 13:39317968 A CCDS31960.1 CCDS31960.1 Transcript intron_variant - - - - - - rs2442355 13:39317968 A 341640 NM_207361.4 Transcript intron_variant - - - - - - rs2167027 13:39322719 C CCDS31960.1 CCDS31960.1 Transcript intron_variant - - - - - - rs2167027 13:39322719 C 341640 NM_207361.4 Transcript intron_variant - - - - - - rs6563644 13:39428543 G ENSESTG00000024407 ENSESTT00000061706 Transcript upstream_gene_variant - - - - - - DISTANCE=1775 rs6563644 13:39428543 G CCDS31960.1 CCDS31960.1 Transcript intron_variant - - - - - - rs6563644 13:39428543 G 341640 NM_207361.4 Transcript intron_variant - - - - - - rs2875242 13:39496578 T - - - intergenic_variant - - - - - - rs9532309 13:39513210 G - - - intergenic_variant - - - - - - rs10454605 13:39519553 T - - - intergenic_variant - - - - - - rs1535777 13:39977913 G 10186 NM_005780.2 Transcript intron_variant - - - - - - rs1535777 13:39977913 G CCDS9369.1 CCDS9369.1 Transcript intron_variant - - - - - - rs1177829 13:39981254 T - ENSR00001508974 RegulatoryFeature regulatory_region_variant - - - - - - rs1177829 13:39981254 T 10186 NM_005780.2 Transcript intron_variant - - - - - - rs1177829 13:39981254 T CCDS9369.1 CCDS9369.1 Transcript intron_variant - - - - - - rs2148935 13:40046262 C 10186 NM_005780.2 Transcript intron_variant - - - - - - rs2148935 13:40046262 C CCDS9369.1 CCDS9369.1 Transcript intron_variant - - - - - - rs2324350 13:40173392 C ENSESTG00000012932 ENSESTT00000032425 Transcript downstream_gene_variant - - - - - - DISTANCE=1846 rs2324350 13:40173392 C 10186 NM_005780.2 Transcript intron_variant - - - - - - rs2324350 13:40173392 C CCDS9369.1 CCDS9369.1 Transcript intron_variant - - - - - - rs2324350 13:40173392 C ENSESTG00000012932 ENSESTT00000032431 Transcript downstream_gene_variant - - - - - - DISTANCE=1704 rs2324350 13:40173392 C ENSESTG00000012932 ENSESTT00000032422 Transcript downstream_gene_variant - - - - - - DISTANCE=2056 rs2324352 13:40176371 T ENSESTG00000012932 ENSESTT00000032425 Transcript intron_variant - - - - - - rs2324352 13:40176371 T 10186 NM_005780.2 Transcript intron_variant - - - - - - rs2324352 13:40176371 T CCDS9369.1 CCDS9369.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1018 rs2324352 13:40176371 T ENSESTG00000012932 ENSESTT00000032431 Transcript intron_variant - - - - - - rs2324352 13:40176371 T ENSESTG00000012932 ENSESTT00000032422 Transcript intron_variant - - - - - - rs9548847 13:40200150 C - - - intergenic_variant - - - - - - rs7337124 13:40345569 G CCDS45042.1 CCDS45042.1 Transcript intron_variant - - - - - - rs7337124 13:40345569 G 57511 NM_001145079.1 Transcript intron_variant - - - - - - rs7337124 13:40345569 G ENSESTG00000012899 ENSESTT00000032397 Transcript intron_variant - - - - - - rs4620840 13:40356164 T CCDS45042.1 CCDS45042.1 Transcript intron_variant - - - - - - rs4620840 13:40356164 T 57511 NM_001145079.1 Transcript intron_variant - - - - - - rs4620840 13:40356164 T ENSESTG00000012899 ENSESTT00000032397 Transcript intron_variant - - - - - - rs9532437 13:40367705 C 57511 NM_001145079.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1903 rs4334156 13:40374729 A - - - intergenic_variant - - - - - - rs7336727 13:40376149 C - - - intergenic_variant - - - - - - rs4318087 13:40376243 A - - - intergenic_variant - - - - - - rs9532441 13:40376456 C - - - intergenic_variant - - - - - - rs7321360 13:40377147 A - - - intergenic_variant - - - - - - rs7326741 13:40377536 T - - - intergenic_variant - - - - - - rs4245397 13:40379280 A - - - intergenic_variant - - - - - - rs7318167 13:40380282 G - - - intergenic_variant - - - - - - rs4633576 13:40380651 G - - - intergenic_variant - - - - - - rs4943701 13:40381740 G - - - intergenic_variant - - - - - - rs7984143 13:40383220 C - - - intergenic_variant - - - - - - rs4473058 13:40384435 T - - - intergenic_variant - - - - - - rs4426232 13:40387002 A - - - intergenic_variant - - - - - - rs4245398 13:40393351 C - ENSR00000514713 RegulatoryFeature regulatory_region_variant - - - - - - rs4245398 13:40393351 C - - - intergenic_variant - - - - - - rs4503676 13:40396791 C - - - intergenic_variant - - - - - - rs6563759 13:40397418 T - - - intergenic_variant - - - - - - rs4943704 13:40406464 G - - - intergenic_variant - - - - - - rs1414931 13:40658313 A ENSESTG00000012927 ENSESTT00000032409 Transcript intron_variant - - - - - - rs7327931 13:40703649 G ENSESTG00000012927 ENSESTT00000032409 Transcript intron_variant - - - - - - rs7993021 13:40705692 G - ENSR00000514767 RegulatoryFeature regulatory_region_variant - - - - - - rs7993021 13:40705692 G ENSESTG00000012927 ENSESTT00000032409 Transcript intron_variant - - - - - - rs4611326 13:40709599 C ENSESTG00000012927 ENSESTT00000032409 Transcript intron_variant - - - - - - rs4943766 13:40894913 G - - - intergenic_variant - - - - - - rs2802508 13:40964428 C 646982 NR_024506.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2802508 13:40964428 C 646982 NR_024507.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4943799 13:41209883 A - ENSR00000514860 RegulatoryFeature regulatory_region_variant - - - - - - rs4943799 13:41209883 A ENSESTG00000006263 ENSESTT00000015788 Transcript intron_variant - - - - - - rs4943799 13:41209883 A ENSESTG00000006263 ENSESTT00000015803 Transcript intron_variant - - - - - - rs4943799 13:41209883 A ENSESTG00000006263 ENSESTT00000015802 Transcript intron_variant - - - - - - rs4943799 13:41209883 A 2308 NM_002015.3 Transcript intron_variant - - - - - - rs4943799 13:41209883 A CCDS9371.1 CCDS9371.1 Transcript intron_variant - - - - - - rs9532708 13:41605448 G ENSESTG00000006205 ENSESTT00000015643 Transcript intron_variant - - - - - - rs9532708 13:41605448 G ENSESTG00000006205 ENSESTT00000015659 Transcript intron_variant - - - - - - rs9532708 13:41605448 G ENSESTG00000006205 ENSESTT00000015632 Transcript intron_variant - - - - - - rs9532708 13:41605448 G ENSESTG00000006205 ENSESTT00000015654 Transcript intron_variant - - - - - - rs9532708 13:41605448 G ENSESTG00000006205 ENSESTT00000015649 Transcript intron_variant - - - - - - rs654267 13:42801173 A 160851 NM_152910.4 Transcript intron_variant - - - - - - rs654267 13:42801173 A ENSESTG00000014761 ENSESTT00000036949 Transcript intron_variant - - - - - - rs654267 13:42801173 A ENSESTG00000014761 ENSESTT00000036969 Transcript intron_variant - - - - - - rs654267 13:42801173 A ENSESTG00000014761 ENSESTT00000036956 Transcript intron_variant - - - - - - rs654267 13:42801173 A CCDS9381.1 CCDS9381.1 Transcript intron_variant - - - - - - rs654267 13:42801173 A 160851 NM_001204506.1 Transcript intron_variant - - - - - - rs654267 13:42801173 A ENSESTG00000014761 ENSESTT00000036940 Transcript intron_variant - - - - - - rs654267 13:42801173 A CCDS55899.1 CCDS55899.1 Transcript intron_variant - - - - - - rs654267 13:42801173 A CCDS55898.1 CCDS55898.1 Transcript intron_variant - - - - - - rs654267 13:42801173 A 160851 NM_001204505.1 Transcript intron_variant - - - - - - rs654267 13:42801173 A 160851 NM_178009.3 Transcript intron_variant - - - - - - rs654267 13:42801173 A 160851 NM_001204504.1 Transcript intron_variant - - - - - - rs654267 13:42801173 A CCDS9382.1 CCDS9382.1 Transcript intron_variant - - - - - - rs346584 13:43100176 G - - - intergenic_variant - - - - - - rs653637 13:43106086 T - - - intergenic_variant - - - - - - rs449658 13:43111545 T - - - intergenic_variant - - - - - - rs432997 13:43112355 T - - - intergenic_variant - - - - - - rs445904 13:43113404 C - - - intergenic_variant - - - - - - rs432801 13:43123206 G - ENSR00000666618 RegulatoryFeature regulatory_region_variant - - - - - - rs432801 13:43123206 G - - - intergenic_variant - - - - - - rs615296 13:43124156 A - - - intergenic_variant - - - - - - rs346602 13:43128129 A - ENSR00000515135 RegulatoryFeature regulatory_region_variant - - - - - - rs346602 13:43128129 A - - - intergenic_variant - - - - - - rs7997824 13:43135682 T 8600 NM_033012.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1190 rs1853857 13:43141091 G 8600 NM_033012.3 Transcript intron_variant - - - - - - rs6561060 13:43150635 T CCDS9385.1 CCDS9385.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4627 rs6561060 13:43150635 T ENSESTG00000014883 ENSESTT00000037264 Transcript intron_variant - - - - - - rs6561060 13:43150635 T CCDS9384.1 CCDS9384.1 Transcript intron_variant - - - - - - rs6561060 13:43150635 T 8600 NM_033012.3 Transcript intron_variant - - - - - - rs6561060 13:43150635 T 8600 NM_003701.3 Transcript intron_variant - - - - - - rs4444231 13:43156152 A CCDS9385.1 CCDS9385.1 Transcript intron_variant - - - - - - rs4444231 13:43156152 A ENSESTG00000014883 ENSESTT00000037264 Transcript intron_variant - - - - - - rs4444231 13:43156152 A CCDS9384.1 CCDS9384.1 Transcript intron_variant - - - - - - rs4444231 13:43156152 A 8600 NM_033012.3 Transcript intron_variant - - - - - - rs4444231 13:43156152 A 8600 NM_003701.3 Transcript intron_variant - - - - - - rs346587 13:43163950 A CCDS9385.1 CCDS9385.1 Transcript intron_variant - - - - - - rs346587 13:43163950 A ENSESTG00000014883 ENSESTT00000037264 Transcript intron_variant - - - - - - rs346587 13:43163950 A CCDS9384.1 CCDS9384.1 Transcript intron_variant - - - - - - rs346587 13:43163950 A 8600 NM_033012.3 Transcript intron_variant - - - - - - rs346587 13:43163950 A 8600 NM_003701.3 Transcript intron_variant - - - - - - rs387856 13:43175462 G CCDS9385.1 CCDS9385.1 Transcript intron_variant - - - - - - rs387856 13:43175462 G ENSESTG00000014883 ENSESTT00000037264 Transcript intron_variant - - - - - - rs387856 13:43175462 G CCDS9384.1 CCDS9384.1 Transcript intron_variant - - - - - - rs387856 13:43175462 G 8600 NM_033012.3 Transcript intron_variant - - - - - - rs387856 13:43175462 G 8600 NM_003701.3 Transcript intron_variant - - - - - - rs2324852 13:43193786 G - - - intergenic_variant - - - - - - rs114257496 13:43214782 T - - - intergenic_variant - - - - - - rs4942174 13:43474371 T ENSESTG00000014933 ENSESTT00000037492 Transcript intron_variant - - - - - - rs4942174 13:43474371 T 94240 NM_033255.3 Transcript intron_variant - - - - - - rs4942174 13:43474371 T ENSESTG00000014900 ENSESTT00000037307 Transcript intron_variant - - - - - - rs4942174 13:43474371 T 94240 NM_001002264.2 Transcript intron_variant - - - - - - rs4942174 13:43474371 T CCDS31964.1 CCDS31964.1 Transcript intron_variant - - - - - - rs4942174 13:43474371 T ENSESTG00000014933 ENSESTT00000037473 Transcript intron_variant - - - - - - rs4942174 13:43474371 T ENSESTG00000014933 ENSESTT00000037496 Transcript downstream_gene_variant - - - - - - DISTANCE=121 rs4942174 13:43474371 T ENSESTG00000014933 ENSESTT00000037477 Transcript intron_variant - - - - - - rs4942174 13:43474371 T CCDS9387.1 CCDS9387.1 Transcript intron_variant - - - - - - rs4942174 13:43474371 T ENSESTG00000014933 ENSESTT00000037482 Transcript intron_variant - - - - - - rs2657121 13:43755873 A - - - intergenic_variant - - - - - - rs7333733 13:43797950 T ENSESTG00000032928 ENSESTT00000083246 Transcript intron_variant - - - - - - rs7333733 13:43797950 T ENSESTG00000032928 ENSESTT00000083245 Transcript downstream_gene_variant - - - - - - DISTANCE=275 rs7333733 13:43797950 T 55068 NM_001127615.1 Transcript intron_variant - - - - - - rs7333733 13:43797950 T CCDS9389.1 CCDS9389.1 Transcript intron_variant - - - - - - rs7333733 13:43797950 T 55068 NM_001242863.1 Transcript intron_variant - - - - - - rs7333733 13:43797950 T 55068 NM_017993.3 Transcript intron_variant - - - - - - rs7317683 13:44318336 C ENSESTG00000032884 ENSESTT00000083155 Transcript intron_variant - - - - - - rs7317683 13:44318336 C ENSESTG00000032884 ENSESTT00000083146 Transcript intron_variant - - - - - - rs7317683 13:44318336 C ENSESTG00000032884 ENSESTT00000083117 Transcript intron_variant - - - - - - rs7317683 13:44318336 C ENSESTG00000032884 ENSESTT00000083133 Transcript intron_variant - - - - - - rs7317683 13:44318336 C 55068 NM_001242863.1 Transcript intron_variant - - - - - - rs7317683 13:44318336 C 55068 NM_017993.3 Transcript intron_variant - - - - - - rs7317683 13:44318336 C ENSESTG00000032884 ENSESTT00000083123 Transcript intron_variant - - - - - - rs4941472 13:44340963 G ENSESTG00000032884 ENSESTT00000083155 Transcript intron_variant - - - - - - rs4941472 13:44340963 G ENSESTG00000032884 ENSESTT00000083146 Transcript intron_variant - - - - - - rs4941472 13:44340963 G ENSESTG00000032884 ENSESTT00000083117 Transcript intron_variant - - - - - - rs4941472 13:44340963 G ENSESTG00000032884 ENSESTT00000083133 Transcript intron_variant - - - - - - rs4941472 13:44340963 G 55068 NM_001242863.1 Transcript intron_variant - - - - - - rs4941472 13:44340963 G 55068 NM_017993.3 Transcript intron_variant - - - - - - rs4941472 13:44340963 G ENSESTG00000032884 ENSESTT00000083123 Transcript intron_variant - - - - - - rs4272924 13:44982202 C - ENSR00000515393 RegulatoryFeature regulatory_region_variant - - - - - - rs4272924 13:44982202 C ENSESTG00000000550 ENSESTT00000001313 Transcript upstream_gene_variant - - - - - - DISTANCE=2200 rs7993412 13:45018823 A CCDS58291.1 CCDS58291.1 Transcript intron_variant - - - - - - rs7993412 13:45018823 A ENSESTG00000000523 ENSESTT00000001285 Transcript intron_variant - - - - - - rs7993412 13:45018823 A 8848 NM_183422.3 Transcript intron_variant - - - - - - rs7993412 13:45018823 A 8848 NM_001243799.1 Transcript intron_variant - - - - - - rs7993412 13:45018823 A 8848 NM_001243798.1 Transcript intron_variant - - - - - - rs7993412 13:45018823 A CCDS31966.1 CCDS31966.1 Transcript intron_variant - - - - - - rs1148316 13:45393241 G - ENSR00000515463 RegulatoryFeature regulatory_region_variant - - - - - - rs1148316 13:45393241 G - - - intergenic_variant - - - - - - rs4463981 13:45952826 G 100190939 NR_024458.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs942892 13:46148365 C 220081 NM_182542.2 Transcript intron_variant - - - - - - rs942892 13:46148365 C CCDS45045.1 CCDS45045.1 Transcript intron_variant - - - - - - rs2764584 13:46890723 C - - - intergenic_variant - - - - - - rs198585 13:49035602 T ENSESTG00000020877 ENSESTT00000052910 Transcript intron_variant - - - - - - rs198585 13:49035602 T ENSESTG00000020877 ENSESTT00000052892 Transcript intron_variant - - - - - - rs198585 13:49035602 T CCDS31973.1 CCDS31973.1 Transcript intron_variant - - - - - - rs198585 13:49035602 T ENSESTG00000020877 ENSESTT00000052916 Transcript intron_variant - - - - - - rs198585 13:49035602 T 5925 NM_000321.2 Transcript intron_variant - - - - - - rs6561473 13:49226194 T - - - intergenic_variant - - - - - - rs972074 13:49314130 G - - - intergenic_variant - - - - - - rs2897612 13:49356238 G - - - intergenic_variant - - - - - - rs1149872 13:49388043 T - - - intergenic_variant - - - - - - rs2596249 13:49484958 C - - - intergenic_variant - - - - - - rs2555784 13:49500804 A - - - intergenic_variant - - - - - - rs357676 13:49511741 C - - - intergenic_variant - - - - - - rs4245349 13:49519658 G - - - intergenic_variant - - - - - - rs1034066 13:49524019 A - - - intergenic_variant - - - - - - rs3012114 13:49583645 A 22862 NM_001079673.1 Transcript intron_variant - - - - - - rs3012114 13:49583645 A ENSESTG00000021112 ENSESTT00000053053 Transcript intron_variant - - - - - - rs3012114 13:49583645 A ENSESTG00000021112 ENSESTT00000053070 Transcript intron_variant - - - - - - rs3012114 13:49583645 A ENSESTG00000021112 ENSESTT00000053012 Transcript intron_variant - - - - - - rs3012114 13:49583645 A CCDS41886.1 CCDS41886.1 Transcript intron_variant - - - - - - rs3012114 13:49583645 A ENSESTG00000021112 ENSESTT00000053042 Transcript intron_variant - - - - - - rs1937179 13:49597411 G 22862 NM_001079673.1 Transcript intron_variant - - - - - - rs1937179 13:49597411 G ENSESTG00000021112 ENSESTT00000053053 Transcript intron_variant - - - - - - rs1937179 13:49597411 G ENSESTG00000021112 ENSESTT00000053070 Transcript intron_variant - - - - - - rs1937179 13:49597411 G ENSESTG00000021112 ENSESTT00000053012 Transcript intron_variant - - - - - - rs1937179 13:49597411 G CCDS41886.1 CCDS41886.1 Transcript intron_variant - - - - - - rs1937179 13:49597411 G ENSESTG00000021112 ENSESTT00000053042 Transcript intron_variant - - - - - - rs2897634 13:49629570 G 22862 NM_001079673.1 Transcript intron_variant - - - - - - rs2897634 13:49629570 G ENSESTG00000021112 ENSESTT00000053078 Transcript intron_variant - - - - - - rs2897634 13:49629570 G ENSESTG00000021112 ENSESTT00000053053 Transcript intron_variant - - - - - - rs2897634 13:49629570 G ENSESTG00000021112 ENSESTT00000053070 Transcript intron_variant - - - - - - rs2897634 13:49629570 G ENSESTG00000021112 ENSESTT00000053012 Transcript intron_variant - - - - - - rs2897634 13:49629570 G CCDS41886.1 CCDS41886.1 Transcript intron_variant - - - - - - rs2897634 13:49629570 G ENSESTG00000021112 ENSESTT00000053042 Transcript intron_variant - - - - - - rs1983807 13:49711252 C CCDS9413.2 CCDS9413.2 Transcript intron_variant - - - - - - rs1983807 13:49711252 C ENSESTG00000021112 ENSESTT00000053070 Transcript downstream_gene_variant - - - - - - DISTANCE=666 rs1983807 13:49711252 C ENSESTG00000021266 ENSESTT00000053376 Transcript downstream_gene_variant - - - - - - DISTANCE=571 rs1983807 13:49711252 C ENSESTG00000021266 ENSESTT00000053442 Transcript intron_variant - - - - - - rs1983807 13:49711252 C 22862 NM_014923.3 Transcript intron_variant - - - - - - rs1983807 13:49711252 C CCDS41886.1 CCDS41886.1 Transcript intron_variant - - - - - - rs1983807 13:49711252 C 22862 NM_001079673.1 Transcript intron_variant - - - - - - rs1983807 13:49711252 C ENSESTG00000021112 ENSESTT00000053012 Transcript downstream_gene_variant - - - - - - DISTANCE=666 rs1983807 13:49711252 C ENSESTG00000021112 ENSESTT00000053042 Transcript downstream_gene_variant - - - - - - DISTANCE=666 rs1983807 13:49711252 C ENSESTG00000021266 ENSESTT00000053412 Transcript downstream_gene_variant - - - - - - DISTANCE=576 rs7330672 13:49818209 C ENSESTG00000022658 ENSESTT00000057166 Transcript intron_variant - - - - - - rs7330672 13:49818209 C ENSESTG00000022658 ENSESTT00000057157 Transcript intron_variant - - - - - - rs7330672 13:49818209 C CCDS9415.1 CCDS9415.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3965 rs7330672 13:49818209 C 81602 NM_030911.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3838 rs7330672 13:49818209 C 81602 NM_001193478.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3838 rs7330672 13:49818209 C ENSESTG00000021590 ENSESTT00000054210 Transcript upstream_gene_variant - - - - - - DISTANCE=3802 rs7330672 13:49818209 C 81602 NR_036439.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3838 rs9535210 13:49937441 A CCDS9416.2 CCDS9416.2 Transcript intron_variant - - - - - - rs9535210 13:49937441 A 81617 NM_001079670.1 Transcript intron_variant - - - - - - rs9535210 13:49937441 A ENSESTG00000022578 ENSESTT00000057089 Transcript intron_variant - - - - - - rs9535210 13:49937441 A 81617 NM_030925.2 Transcript intron_variant - - - - - - rs9535210 13:49937441 A ENSESTG00000022578 ENSESTT00000057038 Transcript intron_variant - - - - - - rs7988060 13:50088357 G CCDS31975.1 CCDS31975.1 Transcript intron_variant - - - - - - rs7988060 13:50088357 G CCDS41887.1 CCDS41887.1 Transcript intron_variant - - - - - - rs7988060 13:50088357 G ENSESTG00000021994 ENSESTT00000055415 Transcript intron_variant - - - - - - rs7988060 13:50088357 G 51131 NM_001040444.1 Transcript intron_variant - - - - - - rs7988060 13:50088357 G ENSESTG00000021994 ENSESTT00000055355 Transcript intron_variant - - - - - - rs7988060 13:50088357 G ENSESTG00000021994 ENSESTT00000055400 Transcript intron_variant - - - - - - rs7988060 13:50088357 G ENSESTG00000021994 ENSESTT00000055377 Transcript downstream_gene_variant - - - - - - DISTANCE=1087 rs7988060 13:50088357 G 51131 NM_001040443.1 Transcript intron_variant - - - - - - rs1209358 13:50381913 C - ENSR00000666709 RegulatoryFeature regulatory_region_variant - - - - - - rs1209358 13:50381913 C - - - intergenic_variant - - - - - - rs2407880 13:50500409 T CCDS9422.1 CCDS9422.1 Transcript intron_variant - - - - - - rs2407880 13:50500409 T 57213 NM_020456.2 Transcript intron_variant - - - - - - rs2407880 13:50500409 T CCDS45046.1 CCDS45046.1 Transcript intron_variant - - - - - - rs2407880 13:50500409 T ENSESTG00000022314 ENSESTT00000056371 Transcript intron_variant - - - - - - rs2407880 13:50500409 T 57213 NM_001127482.1 Transcript intron_variant - - - - - - rs2407880 13:50500409 T ENSESTG00000022314 ENSESTT00000056386 Transcript intron_variant - - - - - - rs2407880 13:50500409 T 57213 NR_023351.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2803836 13:50591480 C 10206 NM_005798.3 Transcript 3_prime_UTR_variant 5632 - - - - - rs2803836 13:50591480 C CCDS9424.1 CCDS9424.1 Transcript intron_variant - - - - - - rs2803836 13:50591480 C ENSESTG00000022244 ENSESTT00000056060 Transcript intron_variant - - - - - - rs2803836 13:50591480 C CCDS41889.1 CCDS41889.1 Transcript intron_variant - - - - - - rs2803836 13:50591480 C CCDS41888.1 CCDS41888.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4180 rs2803836 13:50591480 C 10206 NM_213590.1 Transcript 3_prime_UTR_variant 6167 - - - - - rs2803836 13:50591480 C CCDS9423.1 CCDS9423.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4180 rs2803836 13:50591480 C ENSESTG00000022258 ENSESTT00000056209 Transcript intron_variant - - - - - - rs2803836 13:50591480 C ENSESTG00000022244 ENSESTT00000056093 Transcript intron_variant - - - - - - rs2803836 13:50591480 C 283518 NM_199464.2 Transcript intron_variant - - - - - - rs2803836 13:50591480 C 8847 NR_002612.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2803836 13:50591480 C ENSESTG00000022244 ENSESTT00000056076 Transcript intron_variant - - - - - - rs2803836 13:50591480 C 10206 NM_001007278.1 Transcript 3_prime_UTR_variant 5831 - - - - - rs2803836 13:50591480 C 10206 NM_052811.2 Transcript 3_prime_UTR_variant 5717 - - - - - rs2803836 13:50591480 C 283518 NM_173605.1 Transcript intron_variant - - - - - - rs806353 13:50864639 A - - - intergenic_variant - - - - - - rs201761 13:51012764 A - - - intergenic_variant - - - - - - rs797511 13:51226659 C - - - intergenic_variant - - - - - - rs797508 13:51282239 C 220107 NM_198989.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4520 rs797508 13:51282239 C ENSESTG00000023796 ENSESTT00000059988 Transcript intron_variant - - - - - - rs797508 13:51282239 C ENSESTG00000023810 ENSESTT00000060007 Transcript downstream_gene_variant - - - - - - DISTANCE=4519 rs2476616 13:51302344 G 220107 NM_198989.2 Transcript intron_variant - - - - - - rs2476616 13:51302344 G CCDS53869.1 CCDS53869.1 Transcript intron_variant - - - - - - rs2476616 13:51302344 G ENSESTG00000023420 ENSESTT00000059063 Transcript intron_variant - - - - - - rs2476616 13:51302344 G ENSESTG00000023796 ENSESTT00000059988 Transcript intron_variant - - - - - - rs2476616 13:51302344 G ENSESTG00000023420 ENSESTT00000059054 Transcript intron_variant - - - - - - rs2812239 13:51304446 G 220107 NM_198989.2 Transcript intron_variant - - - - - - rs2812239 13:51304446 G CCDS53869.1 CCDS53869.1 Transcript intron_variant - - - - - - rs2812239 13:51304446 G ENSESTG00000023420 ENSESTT00000059063 Transcript intron_variant - - - - - - rs2812239 13:51304446 G ENSESTG00000023796 ENSESTT00000059988 Transcript intron_variant - - - - - - rs2812239 13:51304446 G ENSESTG00000023420 ENSESTT00000059054 Transcript intron_variant - - - - - - rs1268229 13:51450294 T ENSESTG00000023781 ENSESTT00000059943 Transcript downstream_gene_variant - - - - - - DISTANCE=4776 rs4942944 13:51514307 G CCDS45047.1 CCDS45047.1 Transcript intron_variant - - - - - - rs4942944 13:51514307 G ENSESTG00000023450 ENSESTT00000059291 Transcript intron_variant - - - - - - rs4942944 13:51514307 G ENSESTG00000023450 ENSESTT00000059279 Transcript intron_variant - - - - - - rs4942944 13:51514307 G ENSESTG00000023781 ENSESTT00000059943 Transcript intron_variant - - - - - - rs4942944 13:51514307 G ENSESTG00000023450 ENSESTT00000059202 Transcript intron_variant - - - - - - rs4942944 13:51514307 G ENSESTG00000023450 ENSESTT00000059246 Transcript intron_variant - - - - - - rs4942944 13:51514307 G 79621 NM_024570.3 Transcript intron_variant - - - - - - rs4942944 13:51514307 G ENSESTG00000023450 ENSESTT00000059260 Transcript intron_variant - - - - - - rs4942944 13:51514307 G 79621 NM_001142279.2 Transcript intron_variant - - - - - - rs4942944 13:51514307 G ENSESTG00000023450 ENSESTT00000059240 Transcript intron_variant - - - - - - rs4942944 13:51514307 G ENSESTG00000023450 ENSESTT00000059284 Transcript intron_variant - - - - - - rs4942944 13:51514307 G ENSESTG00000023450 ENSESTT00000059206 Transcript intron_variant - - - - - - rs4942944 13:51514307 G CCDS9425.1 CCDS9425.1 Transcript intron_variant - - - - - - rs4941712 13:52296863 A ENSESTG00000006290 ENSESTT00000015892 Transcript intron_variant - - - - - - rs4941712 13:52296863 A ENSESTG00000006290 ENSESTT00000015874 Transcript downstream_gene_variant - - - - - - DISTANCE=3479 rs4941712 13:52296863 A 115825 NM_052950.3 Transcript intron_variant - - - - - - rs4941712 13:52296863 A CCDS9429.1 CCDS9429.1 Transcript intron_variant - - - - - - rs4586321 13:52746405 T 100887750 NR_051965.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4586321 13:52746405 T ENSESTG00000033370 ENSESTT00000084301 Transcript downstream_gene_variant - - - - - - DISTANCE=3397 rs4586321 13:52746405 T 100887750 NR_051964.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4586321 13:52746405 T 100887750 NR_002816.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs4586321 13:52746405 T ENSESTG00000033370 ENSESTT00000084279 Transcript downstream_gene_variant - - - - - - DISTANCE=3451 rs4586321 13:52746405 T 100887750 NR_051963.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7332119 13:54391166 G 100861552 NR_047488.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1458274 13:54453076 G 100861552 NR_047488.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2822 rs2818211 13:54910243 A - - - intergenic_variant - - - - - - rs263820 13:55540316 C - - - intergenic_variant - - - - - - rs9316756 13:55585841 C - - - intergenic_variant - - - - - - rs2937319 13:56002914 C - - - intergenic_variant - - - - - - rs2997103 13:56317369 A - - - intergenic_variant - - - - - - rs2763576 13:56641421 T - - - intergenic_variant - - - - - - rs185815 13:56648547 T - - - intergenic_variant - - - - - - rs1924912 13:57184952 G - - - intergenic_variant - - - - - - rs914453 13:57322634 T - - - intergenic_variant - - - - - - rs4329816 13:57645584 C - - - intergenic_variant - - - - - - rs601396 13:57710826 C 122183 NM_198441.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4226 rs601396 13:57710826 C CCDS31981.1 CCDS31981.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4613 rs601396 13:57710826 C ENSESTG00000034581 ENSESTT00000087462 Transcript upstream_gene_variant - - - - - - DISTANCE=4226 rs771520 13:58097962 A - - - intergenic_variant - - - - - - rs354776 13:58146863 A - - - intergenic_variant - - - - - - rs540593 13:58655252 T - - - intergenic_variant - - - - - - rs7336081 13:58847422 G - - - intergenic_variant - - - - - - rs6561960 13:58857817 G - - - intergenic_variant - - - - - - rs76525966 13:58859792 G - - - intergenic_variant - - - - - - rs1867605 13:59560437 G - - - intergenic_variant - - - - - - rs9538313 13:59728591 A - - - intergenic_variant - - - - - - rs1327936 13:59746890 C - - - intergenic_variant - - - - - - rs369405 13:60592721 T CCDS58297.1 CCDS58297.1 Transcript intron_variant - - - - - - rs369405 13:60592721 T 100874195 NR_046539.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs369405 13:60592721 T 81624 NM_001258369.1 Transcript intron_variant - - - - - - rs369405 13:60592721 T ENSESTG00000030662 ENSESTT00000077347 Transcript upstream_gene_variant - - - - - - DISTANCE=2582 rs369405 13:60592721 T ENSESTG00000030662 ENSESTT00000077333 Transcript intron_variant - - - - - - rs369405 13:60592721 T ENSESTG00000030662 ENSESTT00000077313 Transcript intron_variant - - - - - - rs369405 13:60592721 T CCDS58296.1 CCDS58296.1 Transcript intron_variant - - - - - - rs369405 13:60592721 T 81624 NM_001258366.1 Transcript intron_variant - - - - - - rs369405 13:60592721 T 81624 NM_001258367.1 Transcript intron_variant - - - - - - rs369405 13:60592721 T CCDS58294.1 CCDS58294.1 Transcript intron_variant - - - - - - rs369405 13:60592721 T 100874195 NR_051994.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs369405 13:60592721 T 81624 NM_001258368.1 Transcript intron_variant - - - - - - rs369405 13:60592721 T ENSESTG00000030427 ENSESTT00000076614 Transcript intron_variant - - - - - - rs369405 13:60592721 T ENSESTG00000030427 ENSESTT00000076606 Transcript intron_variant - - - - - - rs369405 13:60592721 T CCDS41898.1 CCDS41898.1 Transcript intron_variant - - - - - - rs369405 13:60592721 T 100874195 NR_051993.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs369405 13:60592721 T CCDS58295.1 CCDS58295.1 Transcript intron_variant - - - - - - rs369405 13:60592721 T 81624 NM_001042517.1 Transcript intron_variant - - - - - - rs7982963 13:61131408 G 81550 NM_001146071.1 Transcript intron_variant - - - - - - rs7982963 13:61131408 G ENSESTG00000030545 ENSESTT00000077004 Transcript intron_variant - - - - - - rs7982963 13:61131408 G ENSESTG00000030608 ENSESTT00000077051 Transcript downstream_gene_variant - - - - - - DISTANCE=3495 rs7982963 13:61131408 G CCDS53872.1 CCDS53872.1 Transcript intron_variant - - - - - - rs7982963 13:61131408 G 81550 NM_001146070.1 Transcript intron_variant - - - - - - rs7982963 13:61131408 G 81550 NM_030794.2 Transcript intron_variant - - - - - - rs7982963 13:61131408 G CCDS9441.1 CCDS9441.1 Transcript intron_variant - - - - - - rs4886255 13:61269994 A ENSESTG00000030593 ENSESTT00000077026 Transcript downstream_gene_variant - - - - - - DISTANCE=62 rs7324922 13:61309652 A - - - intergenic_variant - - - - - - rs3119853 13:61356005 C - - - intergenic_variant - - - - - - rs7332450 13:61969076 T - - - intergenic_variant - - - - - - rs1332383 13:62491022 T - - - intergenic_variant - - - - - - rs515345 13:62771602 G - - - intergenic_variant - - - - - - rs4375563 13:62890849 T - - - intergenic_variant - - - - - - rs501508 13:63716607 C - - - intergenic_variant - - - - - - rs272300 13:64596437 A ENSESTG00000028148 ENSESTT00000070781 Transcript intron_variant - - - - - - rs1341048 13:64815442 C - - - intergenic_variant - - - - - - rs1415010 13:65126870 C - - - intergenic_variant - - - - - - rs544755 13:65302927 A - - - intergenic_variant - - - - - - rs962543 13:66000785 A - - - intergenic_variant - - - - - - rs9540458 13:66087357 T - - - intergenic_variant - - - - - - rs2184840 13:67135539 G CCDS9444.1 CCDS9444.1 Transcript intron_variant - - - - - - rs2184840 13:67135539 G 5101 NM_020403.4 Transcript intron_variant - - - - - - rs2184840 13:67135539 G 5101 NM_203487.2 Transcript intron_variant - - - - - - rs2184840 13:67135539 G CCDS9443.1 CCDS9443.1 Transcript intron_variant - - - - - - rs7329829 13:67284950 C ENSESTG00000032100 ENSESTT00000080994 Transcript upstream_gene_variant - - - - - - DISTANCE=1128 rs7329829 13:67284950 C CCDS9444.1 CCDS9444.1 Transcript intron_variant - - - - - - rs7329829 13:67284950 C 5101 NM_020403.4 Transcript intron_variant - - - - - - rs7329829 13:67284950 C 5101 NM_203487.2 Transcript intron_variant - - - - - - rs7329829 13:67284950 C CCDS9443.1 CCDS9443.1 Transcript intron_variant - - - - - - rs9317617 13:67398134 T 100874064 NR_046527.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1167 rs9317617 13:67398134 T CCDS9444.1 CCDS9444.1 Transcript intron_variant - - - - - - rs9317617 13:67398134 T ENSESTG00000032085 ENSESTT00000080971 Transcript upstream_gene_variant - - - - - - DISTANCE=1167 rs9317617 13:67398134 T 5101 NM_020403.4 Transcript intron_variant - - - - - - rs9317617 13:67398134 T 5101 NM_203487.2 Transcript intron_variant - - - - - - rs9317617 13:67398134 T CCDS9443.1 CCDS9443.1 Transcript intron_variant - - - - - - rs260155 13:67613039 C CCDS9444.1 CCDS9444.1 Transcript intron_variant - - - - - - rs260155 13:67613039 C 5101 NM_020403.4 Transcript intron_variant - - - - - - rs260155 13:67613039 C 5101 NM_203487.2 Transcript intron_variant - - - - - - rs260155 13:67613039 C CCDS9443.1 CCDS9443.1 Transcript intron_variant - - - - - - rs260167 13:67627619 A CCDS9444.1 CCDS9444.1 Transcript intron_variant - - - - - - rs260167 13:67627619 A 5101 NM_020403.4 Transcript intron_variant - - - - - - rs260167 13:67627619 A 5101 NM_203487.2 Transcript intron_variant - - - - - - rs260167 13:67627619 A CCDS9443.1 CCDS9443.1 Transcript intron_variant - - - - - - rs7997495 13:68266335 G - - - intergenic_variant - - - - - - rs583924 13:69087867 T - - - intergenic_variant - - - - - - rs287430 13:69260969 T - - - intergenic_variant - - - - - - rs2497361 13:69993687 C - - - intergenic_variant - - - - - - rs489149 13:70131992 G - - - intergenic_variant - - - - - - rs570571 13:70137147 A - - - intergenic_variant - - - - - - rs1424300 13:70333600 A CCDS9445.1 CCDS9445.1 Transcript intron_variant - - - - - - rs1424300 13:70333600 A ENSESTG00000011325 ENSESTT00000028465 Transcript intron_variant - - - - - - rs1424300 13:70333600 A 57626 NM_020866.2 Transcript intron_variant - - - - - - rs1424300 13:70333600 A ENSESTG00000011325 ENSESTT00000028460 Transcript intron_variant - - - - - - rs2498523 13:70800343 G - - - intergenic_variant - - - - - - rs7139711 13:70881044 C - - - intergenic_variant - - - - - - rs9317950 13:71128123 G - - - intergenic_variant - - - - - - rs2172938 13:71140088 G - - - intergenic_variant - - - - - - rs962290 13:71149475 T - - - intergenic_variant - - - - - - rs9542416 13:71156524 T - - - intergenic_variant - - - - - - rs7321475 13:71174253 A - - - intergenic_variant - - - - - - rs1390407 13:71188056 C - - - intergenic_variant - - - - - - rs7997920 13:71190177 C - - - intergenic_variant - - - - - - rs6562640 13:71191232 T - - - intergenic_variant - - - - - - rs337951 13:71247841 A - - - intergenic_variant - - - - - - rs337955 13:71253595 C - - - intergenic_variant - - - - - - rs338151 13:71266298 G - - - intergenic_variant - - - - - - rs614667 13:71298256 C - - - intergenic_variant - - - - - - rs1280916 13:71328770 G - - - intergenic_variant - - - - - - rs1937078 13:71430951 A - - - intergenic_variant - - - - - - rs803822 13:71560127 G - - - intergenic_variant - - - - - - rs803845 13:71571421 T - - - intergenic_variant - - - - - - rs1543871 13:71576057 G - - - intergenic_variant - - - - - - rs803851 13:71581709 G - - - intergenic_variant - - - - - - rs803856 13:71584181 C - - - intergenic_variant - - - - - - rs803858 13:71586607 G - - - intergenic_variant - - - - - - rs803793 13:71608296 G - - - intergenic_variant - - - - - - rs803763 13:71646250 G - - - intergenic_variant - - - - - - rs6650348 13:71807939 G - - - intergenic_variant - - - - - - rs2225438 13:72105978 C CCDS53874.1 CCDS53874.1 Transcript intron_variant - - - - - - rs2225438 13:72105978 C CCDS53873.1 CCDS53873.1 Transcript intron_variant - - - - - - rs2225438 13:72105978 C 1602 NM_080759.4 Transcript intron_variant - - - - - - rs2225438 13:72105978 C CCDS41899.1 CCDS41899.1 Transcript intron_variant - - - - - - rs2225438 13:72105978 C ENSESTG00000017162 ENSESTT00000043202 Transcript intron_variant - - - - - - rs2225438 13:72105978 C ENSESTG00000017162 ENSESTT00000043184 Transcript intron_variant - - - - - - rs2225438 13:72105978 C ENSESTG00000017162 ENSESTT00000043194 Transcript intron_variant - - - - - - rs2225438 13:72105978 C ENSESTG00000017162 ENSESTT00000043210 Transcript intron_variant - - - - - - rs2225438 13:72105978 C 1602 NM_004392.5 Transcript intron_variant - - - - - - rs2225438 13:72105978 C ENSESTG00000017162 ENSESTT00000043206 Transcript intron_variant - - - - - - rs2225438 13:72105978 C 1602 NM_080760.4 Transcript intron_variant - - - - - - rs339801 13:72734608 A - - - intergenic_variant - - - - - - rs1729495 13:72949702 G - - - intergenic_variant - - - - - - rs9530018 13:73061687 G - - - intergenic_variant - - - - - - rs1324906 13:74541135 A CCDS9449.1 CCDS9449.1 Transcript intron_variant - - - - - - rs1324906 13:74541135 A ENSESTG00000008383 ENSESTT00000021211 Transcript intron_variant - - - - - - rs1324906 13:74541135 A 11278 NM_007249.4 Transcript intron_variant - - - - - - rs1324906 13:74541135 A ENSESTG00000008383 ENSESTT00000021222 Transcript intron_variant - - - - - - rs1324906 13:74541135 A ENSESTG00000008383 ENSESTT00000021190 Transcript intron_variant - - - - - - rs1324906 13:74541135 A ENSESTG00000008383 ENSESTT00000021179 Transcript intron_variant - - - - - - rs1324906 13:74541135 A ENSESTG00000008383 ENSESTT00000021232 Transcript intron_variant - - - - - - rs7317404 13:74654995 A ENSESTG00000008383 ENSESTT00000021211 Transcript intron_variant - - - - - - rs7317404 13:74654995 A 11278 NM_007249.4 Transcript intron_variant - - - - - - rs7317404 13:74654995 A ENSESTG00000005314 ENSESTT00000013514 Transcript intron_variant - - - - - - rs7317404 13:74654995 A ENSESTG00000008383 ENSESTT00000021222 Transcript intron_variant - - - - - - rs7317404 13:74654995 A ENSESTG00000008383 ENSESTT00000021190 Transcript intron_variant - - - - - - rs7317404 13:74654995 A ENSESTG00000008383 ENSESTT00000021179 Transcript intron_variant - - - - - - rs9573358 13:74766980 A - - - intergenic_variant - - - - - - rs9318249 13:74781163 G - - - intergenic_variant - - - - - - rs7996426 13:74930440 T ENSESTG00000005286 ENSESTT00000013453 Transcript intron_variant - - - - - - rs1931913 13:75035229 A - - - intergenic_variant - - - - - - rs1326709 13:75078759 T - - - intergenic_variant - - - - - - rs1536412 13:75139100 T - - - intergenic_variant - - - - - - rs1536414 13:75140896 C - - - intergenic_variant - - - - - - rs1326730 13:75144441 T - ENSR00001510601 RegulatoryFeature regulatory_region_variant - - - - - - rs1326730 13:75144441 T - - - intergenic_variant - - - - - - rs2325633 13:75148884 C - - - intergenic_variant - - - - - - rs7327802 13:75269309 A - ENSR00001510611 RegulatoryFeature regulatory_region_variant - - - - - - rs7327802 13:75269309 A - - - intergenic_variant - - - - - - rs1831112 13:75270512 C - - - intergenic_variant - - - - - - rs4885223 13:75271003 T - - - intergenic_variant - - - - - - rs7320369 13:75275210 T - - - intergenic_variant - - - - - - rs2328909 13:75288902 T - - - intergenic_variant - - - - - - rs2328912 13:75295758 G - - - intergenic_variant - - - - - - rs1819322 13:75297060 A - - - intergenic_variant - - - - - - rs9543761 13:75300329 G - - - intergenic_variant - - - - - - rs1327737 13:75363265 T - - - intergenic_variant - - - - - - rs1090422 13:75522591 G - - - intergenic_variant - - - - - - rs1934866 13:75608228 G - - - intergenic_variant - - - - - - rs9543838 13:75617233 A - - - intergenic_variant - - - - - - rs7322848 13:76238173 G CCDS9454.1 CCDS9454.1 Transcript intron_variant - - - - - - rs7322848 13:76238173 G ENSESTG00000010374 ENSESTT00000025948 Transcript intron_variant - - - - - - rs7322848 13:76238173 G 4008 NM_005358.5 Transcript intron_variant - - - - - - rs2663229 13:76683092 G - - - intergenic_variant - - - - - - rs2663231 13:76687170 C - - - intergenic_variant - - - - - - rs2663232 13:76688057 C - - - intergenic_variant - - - - - - rs2663233 13:76689458 A - - - intergenic_variant - - - - - - rs2810428 13:76692552 G - - - intergenic_variant - - - - - - rs2810429 13:76693168 G - - - intergenic_variant - - - - - - rs2810430 13:76699329 A - - - intergenic_variant - - - - - - rs2773997 13:76700189 T - - - intergenic_variant - - - - - - rs2773996 13:76701578 T - - - intergenic_variant - - - - - - rs2663228 13:76727933 C - - - intergenic_variant - - - - - - rs2810437 13:76735422 T - ENSR00000517854 RegulatoryFeature regulatory_region_variant - - - - - - rs2810437 13:76735422 T - - - intergenic_variant - - - - - - rs184019 13:77080625 G - - - intergenic_variant - - - - - - rs399106 13:77092028 A - - - intergenic_variant - - - - - - rs1590838 13:77288395 C - - - intergenic_variant - - - - - - rs7490815 13:77386800 A - ENSR00001510792 RegulatoryFeature regulatory_region_variant - - - - - - rs7490815 13:77386800 A - - - intergenic_variant - - - - - - rs660982 13:77512878 A - - - intergenic_variant - - - - - - rs4884061 13:77851580 T 23077 NM_015057.4 Transcript intron_variant - - - - - - rs4884061 13:77851580 T ENSESTG00000004527 ENSESTT00000011442 Transcript intron_variant - - - - - - rs1144377 13:78302265 A ENSESTG00000009488 ENSESTT00000023830 Transcript upstream_gene_variant - - - - - - DISTANCE=1698 rs1144377 13:78302265 A ENSESTG00000009488 ENSESTT00000023798 Transcript intron_variant - - - - - - rs1144377 13:78302265 A 122060 NM_001040153.3 Transcript intron_variant - - - - - - rs1144377 13:78302265 A ENSESTG00000009488 ENSESTT00000023816 Transcript intron_variant - - - - - - rs1144377 13:78302265 A ENSESTG00000009488 ENSESTT00000023823 Transcript intron_variant - - - - - - rs1144377 13:78302265 A 122060 NM_001242868.1 Transcript intron_variant - - - - - - rs1144377 13:78302265 A CCDS31995.2 CCDS31995.2 Transcript intron_variant - - - - - - rs635020 13:78425480 G ENSESTG00000004518 ENSESTT00000011407 Transcript intron_variant - - - - - - rs1924915 13:78516708 G 100874171 NR_047024.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1924915 13:78516708 G 1910 NM_000115.3 Transcript intron_variant - - - - - - rs2243645 13:78923000 T 100874222 NR_047001.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1218309 13:79420398 T - - - intergenic_variant - - - - - - rs2991490 13:79734208 G - - - intergenic_variant - - - - - - rs4290372 13:80054884 G CCDS31998.1 CCDS31998.1 Transcript upstream_gene_variant - - - - - - DISTANCE=455 rs4290372 13:80054884 G 100874208 NR_046685.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4290372 13:80054884 G ENSESTG00000010531 ENSESTT00000026372 Transcript upstream_gene_variant - - - - - - DISTANCE=562 rs4290372 13:80054884 G 54602 NM_019080.2 Transcript upstream_gene_variant - - - - - - DISTANCE=375 rs4290372 13:80054884 G 54602 NM_001161407.1 Transcript upstream_gene_variant - - - - - - DISTANCE=375 rs3850069 13:80596369 A - - - intergenic_variant - - - - - - rs482985 13:80962419 A - - - intergenic_variant - - - - - - rs1779844 13:81193590 A - - - intergenic_variant - - - - - - rs2794225 13:81255756 T - - - intergenic_variant - - - - - - rs7983091 13:81371218 T - - - intergenic_variant - - - - - - rs6563194 13:81409578 A - - - intergenic_variant - - - - - - rs9545578 13:81520741 A ENSESTG00000012162 ENSESTT00000030425 Transcript downstream_gene_variant - - - - - - DISTANCE=4715 rs261458 13:82329013 C ENSESTG00000012159 ENSESTT00000030418 Transcript intron_variant - - - - - - rs261508 13:82411128 C - - - intergenic_variant - - - - - - rs1577703 13:82462802 G - - - intergenic_variant - - - - - - rs7991088 13:82942037 C - - - intergenic_variant - - - - - - rs1577533 13:82967253 C - - - intergenic_variant - - - - - - rs9546195 13:83195357 T - - - intergenic_variant - - - - - - rs1333591 13:83197222 T - - - intergenic_variant - - - - - - rs4536352 13:84097663 C - - - intergenic_variant - - - - - - rs6563355 13:84143334 G - - - intergenic_variant - - - - - - rs9565922 13:84785646 G 100874128 NR_046871.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1500678 13:85748465 C - - - intergenic_variant - - - - - - rs7332978 13:85947607 C - ENSR00001511102 RegulatoryFeature regulatory_region_variant - - - - - - rs7332978 13:85947607 C 100874137 NR_046989.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7332978 13:85947607 C ENSESTG00000033380 ENSESTT00000084275 Transcript intron_variant - - - - - - rs2184264 13:86728966 C ENSESTG00000016884 ENSESTT00000042363 Transcript intron_variant - - - - - - rs7985188 13:87706525 A - - - intergenic_variant - - - - - - rs2184500 13:88236169 G ENSESTG00000021985 ENSESTT00000055340 Transcript intron_variant - - - - - - rs2184500 13:88236169 G ENSESTG00000021985 ENSESTT00000055460 Transcript intron_variant - - - - - - rs2184500 13:88236169 G ENSESTG00000021985 ENSESTT00000055443 Transcript intron_variant - - - - - - rs2184500 13:88236169 G 642345 NR_033829.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2184500 13:88236169 G ENSESTG00000021985 ENSESTT00000055384 Transcript downstream_gene_variant - - - - - - DISTANCE=1108 rs9557350 13:88280752 C ENSESTG00000021985 ENSESTT00000055340 Transcript intron_variant - - - - - - rs9557350 13:88280752 C ENSESTG00000021985 ENSESTT00000055460 Transcript intron_variant - - - - - - rs9557350 13:88280752 C ENSESTG00000021985 ENSESTT00000055443 Transcript intron_variant - - - - - - rs9557350 13:88280752 C 642345 NR_033829.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9557350 13:88280752 C ENSESTG00000021985 ENSESTT00000055405 Transcript intron_variant - - - - - - rs9557350 13:88280752 C ENSESTG00000021985 ENSESTT00000055384 Transcript intron_variant - - - - - - rs9557350 13:88280752 C ENSESTG00000021985 ENSESTT00000055417 Transcript intron_variant - - - - - - rs3013629 13:88310070 A ENSESTG00000021985 ENSESTT00000055340 Transcript intron_variant - - - - - - rs3013629 13:88310070 A ENSESTG00000021985 ENSESTT00000055460 Transcript intron_variant - - - - - - rs3013629 13:88310070 A ENSESTG00000021985 ENSESTT00000055443 Transcript intron_variant - - - - - - rs3013629 13:88310070 A 642345 NR_033829.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3013629 13:88310070 A ENSESTG00000021985 ENSESTT00000055405 Transcript intron_variant - - - - - - rs3013629 13:88310070 A ENSESTG00000021985 ENSESTT00000055384 Transcript intron_variant - - - - - - rs3013629 13:88310070 A ENSESTG00000021985 ENSESTT00000055417 Transcript intron_variant - - - - - - rs1030424 13:88753530 C - - - intergenic_variant - - - - - - rs7982456 13:88887093 G - - - intergenic_variant - - - - - - rs4280103 13:88904937 C - - - intergenic_variant - - - - - - rs7993078 13:88931119 G - - - intergenic_variant - - - - - - rs445799 13:89056014 A - - - intergenic_variant - - - - - - rs2347145 13:89192076 T ENSESTG00000006146 ENSESTT00000015471 Transcript upstream_gene_variant - - - - - - DISTANCE=2081 rs2347145 13:89192076 T ENSESTG00000006146 ENSESTT00000015478 Transcript upstream_gene_variant - - - - - - DISTANCE=2466 rs2347145 13:89192076 T 100874168 NR_047021.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1008 rs7339246 13:89360963 G - - - intergenic_variant - - - - - - rs4238288 13:89704192 T - - - intergenic_variant - - - - - - rs314409 13:89792417 C - - - intergenic_variant - - - - - - rs314393 13:89817391 T - - - intergenic_variant - - - - - - rs7324711 13:91167337 C ENSESTG00000021063 ENSESTT00000052860 Transcript intron_variant - - - - - - rs2253510 13:91557259 A 144776 NR_027039.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4773621 13:91892460 T - - - intergenic_variant - - - - - - rs2351703 13:91928819 G ENSESTG00000013067 ENSESTT00000032776 Transcript upstream_gene_variant - - - - - - DISTANCE=3944 rs2351703 13:91928819 G ENSESTG00000013067 ENSESTT00000032779 Transcript upstream_gene_variant - - - - - - DISTANCE=3985 rs1953620 13:92198805 A CCDS9468.1 CCDS9468.1 Transcript intron_variant - - - - - - rs1953620 13:92198805 A 2262 NM_004466.4 Transcript intron_variant - - - - - - rs1953618 13:92199053 T CCDS9468.1 CCDS9468.1 Transcript intron_variant - - - - - - rs1953618 13:92199053 T 2262 NM_004466.4 Transcript intron_variant - - - - - - rs4771840 13:92204169 A CCDS9468.1 CCDS9468.1 Transcript intron_variant - - - - - - rs4771840 13:92204169 A 2262 NM_004466.4 Transcript intron_variant - - - - - - rs308228 13:93651228 G - - - intergenic_variant - - - - - - rs2813625 13:94108637 T CCDS9469.1 CCDS9469.1 Transcript intron_variant - - - - - - rs2813625 13:94108637 T 10082 NM_005708.3 Transcript intron_variant - - - - - - rs9516300 13:94499482 G - ENSR00001511377 RegulatoryFeature regulatory_region_variant - - - - - - rs9516300 13:94499482 G 100873973 NR_046536.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9516300 13:94499482 G CCDS9469.1 CCDS9469.1 Transcript intron_variant - - - - - - rs9516300 13:94499482 G 10082 NM_005708.3 Transcript intron_variant - - - - - - rs4773832 13:95600631 A - ENSR00000518957 RegulatoryFeature regulatory_region_variant - - - - - - rs4773832 13:95600631 A - - - intergenic_variant - - - - - - rs9524779 13:95689942 T CCDS9474.1 CCDS9474.1 Transcript intron_variant - - - - - - rs9524779 13:95689942 T ENSESTG00000034973 ENSESTT00000088401 Transcript intron_variant - - - - - - rs9524779 13:95689942 T ENSESTG00000034970 ENSESTT00000088376 Transcript intron_variant - - - - - - rs9524779 13:95689942 T ENSESTG00000034973 ENSESTT00000088403 Transcript intron_variant - - - - - - rs9524779 13:95689942 T 10257 NM_005845.3 Transcript intron_variant - - - - - - rs9524971 13:96077402 G ENSESTG00000034937 ENSESTT00000088304 Transcript intron_variant - - - - - - rs7331559 13:96235913 A 9071 NM_006984.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3903 rs7331559 13:96235913 A CCDS9477.1 CCDS9477.1 Transcript intron_variant - - - - - - rs7331559 13:96235913 A 22873 NM_198968.3 Transcript intron_variant - - - - - - rs7331559 13:96235913 A ENSESTG00000034919 ENSESTT00000088289 Transcript intron_variant - - - - - - rs7331559 13:96235913 A 22873 NM_014934.4 Transcript intron_variant - - - - - - rs7331559 13:96235913 A ENSESTG00000034919 ENSESTT00000088296 Transcript intron_variant - - - - - - rs7331559 13:96235913 A 9071 NM_001160100.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3903 rs7331559 13:96235913 A 9071 NM_182848.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3903 rs7331559 13:96235913 A CCDS9478.1 CCDS9478.1 Transcript intron_variant - - - - - - rs7331559 13:96235913 A ENSESTG00000034919 ENSESTT00000088287 Transcript intron_variant - - - - - - rs2389569 13:96587697 T CCDS9480.1 CCDS9480.1 Transcript intron_variant - - - - - - rs2389569 13:96587697 T 55757 NM_020121.3 Transcript intron_variant - - - - - - rs2389569 13:96587697 T ENSESTG00000031888 ENSESTT00000080469 Transcript intron_variant - - - - - - rs1327624 13:96822462 G CCDS9481.1 CCDS9481.1 Transcript intron_variant - - - - - - rs1327624 13:96822462 G 266722 NM_153456.3 Transcript intron_variant - - - - - - rs639039 13:97347193 C CCDS9481.1 CCDS9481.1 Transcript intron_variant - - - - - - rs639039 13:97347193 C 266722 NM_153456.3 Transcript intron_variant - - - - - - rs9516777 13:97519099 A - - - intergenic_variant - - - - - - rs2809162 13:98495607 G - - - intergenic_variant - - - - - - rs1337784 13:98554841 C - - - intergenic_variant - - - - - - rs1669249 13:98825649 C - ENSR00000519311 RegulatoryFeature regulatory_region_variant - - - - - - rs1669249 13:98825649 C 10160 NM_005766.2 Transcript intron_variant - - - - - - rs1669249 13:98825649 C 140432 NM_178861.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2390 rs1669249 13:98825649 C CCDS9486.1 CCDS9486.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2768 rs1669249 13:98825649 C ENSESTG00000033633 ENSESTT00000085214 Transcript intron_variant - - - - - - rs1669249 13:98825649 C ENSESTG00000033633 ENSESTT00000085221 Transcript intron_variant - - - - - - rs1669249 13:98825649 C 10160 NM_001001715.2 Transcript intron_variant - - - - - - rs1669249 13:98825649 C ENSESTG00000033633 ENSESTT00000085203 Transcript intron_variant - - - - - - rs1669249 13:98825649 C ENSESTG00000033633 ENSESTT00000085227 Transcript intron_variant - - - - - - rs4772072 13:99052514 C 10160 NM_005766.2 Transcript intron_variant - - - - - - rs4772072 13:99052514 C ENSESTG00000033633 ENSESTT00000085255 Transcript intron_variant - - - - - - rs4772072 13:99052514 C ENSESTG00000033633 ENSESTT00000085248 Transcript intron_variant - - - - - - rs4772072 13:99052514 C ENSESTG00000033633 ENSESTT00000085214 Transcript intron_variant - - - - - - rs4772072 13:99052514 C ENSESTG00000033633 ENSESTT00000085221 Transcript intron_variant - - - - - - rs4772072 13:99052514 C ENSESTG00000033633 ENSESTT00000085253 Transcript intron_variant - - - - - - rs4772072 13:99052514 C ENSESTG00000033633 ENSESTT00000085203 Transcript intron_variant - - - - - - rs4772072 13:99052514 C CCDS9487.1 CCDS9487.1 Transcript intron_variant - - - - - - rs2146998 13:99093094 C 10160 NM_005766.2 Transcript splice_region_variant,intron_variant - - - - - - rs2146998 13:99093094 C ENSESTG00000033633 ENSESTT00000085253 Transcript downstream_gene_variant - - - - - - DISTANCE=4739 rs2146998 13:99093094 C ENSESTG00000033633 ENSESTT00000085214 Transcript downstream_gene_variant - - - - - - DISTANCE=4739 rs2146998 13:99093094 C ENSESTG00000033633 ENSESTT00000085203 Transcript downstream_gene_variant - - - - - - DISTANCE=14 rs2146998 13:99093094 C CCDS9487.1 CCDS9487.1 Transcript splice_region_variant,intron_variant - - - - - - rs2146998 13:99093094 C ENSESTG00000033633 ENSESTT00000085248 Transcript downstream_gene_variant - - - - - - DISTANCE=14 rs9517307 13:99098033 A - ENSR00000056598 RegulatoryFeature regulatory_region_variant - - - - - - rs9517307 13:99098033 A ENSESTG00000033725 ENSESTT00000085294 Transcript upstream_gene_variant - - - - - - DISTANCE=352 rs9517307 13:99098033 A 8428 NM_003576.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4422 rs9517307 13:99098033 A 10160 NM_005766.2 Transcript intron_variant - - - - - - rs9517307 13:99098033 A ENSESTG00000033633 ENSESTT00000085203 Transcript downstream_gene_variant - - - - - - DISTANCE=4953 rs9517307 13:99098033 A 8428 NM_001032296.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4422 rs9517307 13:99098033 A CCDS9487.1 CCDS9487.1 Transcript intron_variant - - - - - - rs9517307 13:99098033 A ENSESTG00000033633 ENSESTT00000085248 Transcript downstream_gene_variant - - - - - - DISTANCE=4953 rs6491433 13:99262199 G - - - intergenic_variant - - - - - - rs9300514 13:99477263 G CCDS45062.1 CCDS45062.1 Transcript intron_variant - - - - - - rs9300514 13:99477263 G ENSESTG00000017852 ENSESTT00000045308 Transcript intron_variant - - - - - - rs9300514 13:99477263 G ENSESTG00000017852 ENSESTT00000045117 Transcript intron_variant - - - - - - rs9300514 13:99477263 G ENSESTG00000017852 ENSESTT00000045291 Transcript intron_variant - - - - - - rs9300514 13:99477263 G ENSESTG00000017852 ENSESTT00000045145 Transcript intron_variant - - - - - - rs9300514 13:99477263 G 23348 NM_015296.2 Transcript intron_variant - - - - - - rs9300514 13:99477263 G ENSESTG00000017852 ENSESTT00000045241 Transcript intron_variant - - - - - - rs9300514 13:99477263 G 23348 NM_001130048.1 Transcript intron_variant - - - - - - rs9300514 13:99477263 G ENSESTG00000017852 ENSESTT00000045106 Transcript intron_variant - - - - - - rs9300514 13:99477263 G ENSESTG00000017852 ENSESTT00000045154 Transcript intron_variant - - - - - - rs9300514 13:99477263 G ENSESTG00000017852 ENSESTT00000045138 Transcript intron_variant - - - - - - rs9517469 13:99517654 C CCDS45062.1 CCDS45062.1 Transcript intron_variant - - - - - - rs9517469 13:99517654 C 23348 NM_001130050.1 Transcript intron_variant - - - - - - rs9517469 13:99517654 C ENSESTG00000017852 ENSESTT00000045115 Transcript downstream_gene_variant - - - - - - DISTANCE=1675 rs9517469 13:99517654 C ENSESTG00000017852 ENSESTT00000045117 Transcript intron_variant - - - - - - rs9517469 13:99517654 C 23348 NM_001130049.1 Transcript intron_variant - - - - - - rs9517469 13:99517654 C 23348 NM_015296.2 Transcript intron_variant - - - - - - rs9517469 13:99517654 C CCDS45063.1 CCDS45063.1 Transcript intron_variant - - - - - - rs9517469 13:99517654 C ENSESTG00000017852 ENSESTT00000045125 Transcript downstream_gene_variant - - - - - - DISTANCE=1675 rs9517469 13:99517654 C 23348 NM_001130048.1 Transcript intron_variant - - - - - - rs9517469 13:99517654 C ENSESTG00000017852 ENSESTT00000045106 Transcript intron_variant - - - - - - rs6491461 13:99534048 A CCDS45062.1 CCDS45062.1 Transcript intron_variant - - - - - - rs6491461 13:99534048 A 23348 NM_001130050.1 Transcript intron_variant - - - - - - rs6491461 13:99534048 A ENSESTG00000017762 ENSESTT00000044919 Transcript downstream_gene_variant - - - - - - DISTANCE=3936 rs6491461 13:99534048 A ENSESTG00000017852 ENSESTT00000045115 Transcript intron_variant - - - - - - rs6491461 13:99534048 A ENSESTG00000017852 ENSESTT00000045117 Transcript intron_variant - - - - - - rs6491461 13:99534048 A 23348 NM_001130049.1 Transcript intron_variant - - - - - - rs6491461 13:99534048 A 23348 NM_015296.2 Transcript intron_variant - - - - - - rs6491461 13:99534048 A CCDS45063.1 CCDS45063.1 Transcript intron_variant - - - - - - rs6491461 13:99534048 A ENSESTG00000017852 ENSESTT00000045125 Transcript intron_variant - - - - - - rs6491461 13:99534048 A 23348 NM_001130048.1 Transcript intron_variant - - - - - - rs6491461 13:99534048 A ENSESTG00000017852 ENSESTT00000045106 Transcript intron_variant - - - - - - rs6491462 13:99534712 C CCDS45062.1 CCDS45062.1 Transcript intron_variant - - - - - - rs6491462 13:99534712 C 23348 NM_001130050.1 Transcript intron_variant - - - - - - rs6491462 13:99534712 C ENSESTG00000017762 ENSESTT00000044919 Transcript downstream_gene_variant - - - - - - DISTANCE=3272 rs6491462 13:99534712 C ENSESTG00000017852 ENSESTT00000045115 Transcript intron_variant - - - - - - rs6491462 13:99534712 C ENSESTG00000017852 ENSESTT00000045117 Transcript upstream_gene_variant - - - - - - DISTANCE=449 rs6491462 13:99534712 C 23348 NM_001130049.1 Transcript intron_variant - - - - - - rs6491462 13:99534712 C 23348 NM_015296.2 Transcript intron_variant - - - - - - rs6491462 13:99534712 C CCDS45063.1 CCDS45063.1 Transcript intron_variant - - - - - - rs6491462 13:99534712 C ENSESTG00000017852 ENSESTT00000045125 Transcript upstream_gene_variant - - - - - - DISTANCE=449 rs6491462 13:99534712 C 23348 NM_001130048.1 Transcript intron_variant - - - - - - rs6491462 13:99534712 C ENSESTG00000017852 ENSESTT00000045106 Transcript intron_variant - - - - - - rs7986473 13:99563083 C - ENSR00000519450 RegulatoryFeature regulatory_region_variant - - - - - - rs7986473 13:99563083 C ENSESTG00000017762 ENSESTT00000044805 Transcript intron_variant - - - - - - rs7986473 13:99563083 C CCDS45062.1 CCDS45062.1 Transcript intron_variant - - - - - - rs7986473 13:99563083 C 23348 NM_001130050.1 Transcript intron_variant - - - - - - rs7986473 13:99563083 C 23348 NM_001130049.1 Transcript intron_variant - - - - - - rs7986473 13:99563083 C ENSESTG00000017762 ENSESTT00000044831 Transcript intron_variant - - - - - - rs7986473 13:99563083 C 23348 NM_015296.2 Transcript intron_variant - - - - - - rs7986473 13:99563083 C CCDS45063.1 CCDS45063.1 Transcript intron_variant - - - - - - rs7986473 13:99563083 C ENSESTG00000017762 ENSESTT00000044817 Transcript intron_variant - - - - - - rs7986473 13:99563083 C ENSESTG00000017762 ENSESTT00000044838 Transcript intron_variant - - - - - - rs7986473 13:99563083 C 23348 NM_001130048.1 Transcript intron_variant - - - - - - rs56688373 13:99570835 C ENSESTG00000017762 ENSESTT00000044805 Transcript intron_variant - - - - - - rs56688373 13:99570835 C CCDS45062.1 CCDS45062.1 Transcript intron_variant - - - - - - rs56688373 13:99570835 C 23348 NM_001130050.1 Transcript intron_variant - - - - - - rs56688373 13:99570835 C 23348 NM_001130049.1 Transcript intron_variant - - - - - - rs56688373 13:99570835 C ENSESTG00000017762 ENSESTT00000044831 Transcript intron_variant - - - - - - rs56688373 13:99570835 C 23348 NM_015296.2 Transcript intron_variant - - - - - - rs56688373 13:99570835 C CCDS45063.1 CCDS45063.1 Transcript intron_variant - - - - - - rs56688373 13:99570835 C ENSESTG00000017762 ENSESTT00000044817 Transcript intron_variant - - - - - - rs56688373 13:99570835 C ENSESTG00000017762 ENSESTT00000044838 Transcript intron_variant - - - - - - rs56688373 13:99570835 C 23348 NM_001130048.1 Transcript intron_variant - - - - - - rs8002259 13:99635386 T - ENSR00000519471 RegulatoryFeature regulatory_region_variant - - - - - - rs8002259 13:99635386 T ENSESTG00000017762 ENSESTT00000044817 Transcript intron_variant - - - - - - rs8002259 13:99635386 T ENSESTG00000017762 ENSESTT00000044805 Transcript intron_variant - - - - - - rs8002259 13:99635386 T 23348 NM_001130049.1 Transcript intron_variant - - - - - - rs8002259 13:99635386 T 23348 NM_015296.2 Transcript intron_variant - - - - - - rs6491481 13:99732056 G ENSESTG00000017762 ENSESTT00000044805 Transcript intron_variant - - - - - - rs6491481 13:99732056 G 23348 NM_001130049.1 Transcript intron_variant - - - - - - rs6491481 13:99732056 G 23348 NM_015296.2 Transcript intron_variant - - - - - - rs2390190 13:99748065 G - - - intergenic_variant - - - - - - rs1964897 13:99997183 T ENSESTG00000017474 ENSESTT00000044182 Transcript intron_variant - - - - - - rs1964897 13:99997183 T ENSESTG00000017474 ENSESTT00000044142 Transcript intron_variant - - - - - - rs1964897 13:99997183 T ENSESTG00000017474 ENSESTT00000044131 Transcript intron_variant - - - - - - rs1964897 13:99997183 T CCDS9490.1 CCDS9490.1 Transcript intron_variant - - - - - - rs1964897 13:99997183 T CCDS45064.1 CCDS45064.1 Transcript intron_variant - - - - - - rs1964897 13:99997183 T ENSESTG00000017474 ENSESTT00000044193 Transcript intron_variant - - - - - - rs1964897 13:99997183 T 337867 NR_026644.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1964897 13:99997183 T 337867 NM_177967.3 Transcript intron_variant - - - - - - rs1964897 13:99997183 T 337867 NM_001144072.1 Transcript intron_variant - - - - - - rs1964897 13:99997183 T ENSESTG00000017474 ENSESTT00000044179 Transcript intron_variant - - - - - - rs2793737 13:100349355 G ENSESTG00000017699 ENSESTT00000044677 Transcript intron_variant - - - - - - rs2793737 13:100349355 G ENSESTG00000017699 ENSESTT00000044653 Transcript intron_variant - - - - - - rs2793737 13:100349355 G 171425 NM_206808.2 Transcript intron_variant - - - - - - rs2793737 13:100349355 G CCDS32002.1 CCDS32002.1 Transcript intron_variant - - - - - - rs2806304 13:100457582 G ENSESTG00000026791 ENSESTT00000067535 Transcript intron_variant - - - - - - rs2806304 13:100457582 G ENSESTG00000017699 ENSESTT00000044677 Transcript intron_variant - - - - - - rs2806304 13:100457582 G ENSESTG00000017699 ENSESTT00000044653 Transcript intron_variant - - - - - - rs2806304 13:100457582 G 171425 NM_206808.2 Transcript intron_variant - - - - - - rs2806304 13:100457582 G CCDS32002.1 CCDS32002.1 Transcript intron_variant - - - - - - rs2806304 13:100457582 G ENSESTG00000026791 ENSESTT00000067524 Transcript intron_variant - - - - - - rs2806304 13:100457582 G ENSESTG00000027171 ENSESTT00000068470 Transcript intron_variant - - - - - - rs7324843 13:100785032 A ENSESTG00000026853 ENSESTT00000068177 Transcript intron_variant - - - - - - rs7324843 13:100785032 A ENSESTG00000026853 ENSESTT00000068154 Transcript intron_variant - - - - - - rs7324843 13:100785032 A CCDS45065.1 CCDS45065.1 Transcript intron_variant - - - - - - rs7324843 13:100785032 A ENSESTG00000026853 ENSESTT00000068158 Transcript intron_variant - - - - - - rs7324843 13:100785032 A CCDS9496.2 CCDS9496.2 Transcript intron_variant - - - - - - rs7324843 13:100785032 A 5095 NM_001178004.1 Transcript intron_variant - - - - - - rs7324843 13:100785032 A 5095 NM_000282.3 Transcript intron_variant - - - - - - rs7324843 13:100785032 A 5095 NM_001127692.2 Transcript intron_variant - - - - - - rs7324843 13:100785032 A ENSESTG00000026853 ENSESTT00000068166 Transcript intron_variant - - - - - - rs7324843 13:100785032 A ENSESTG00000026853 ENSESTT00000068191 Transcript intron_variant - - - - - - rs7324843 13:100785032 A CCDS53878.1 CCDS53878.1 Transcript intron_variant - - - - - - rs1953696 13:100805582 T ENSESTG00000026853 ENSESTT00000068177 Transcript intron_variant - - - - - - rs1953696 13:100805582 T ENSESTG00000026853 ENSESTT00000068154 Transcript intron_variant - - - - - - rs1953696 13:100805582 T CCDS45065.1 CCDS45065.1 Transcript intron_variant - - - - - - rs1953696 13:100805582 T ENSESTG00000026853 ENSESTT00000068158 Transcript intron_variant - - - - - - rs1953696 13:100805582 T CCDS9496.2 CCDS9496.2 Transcript intron_variant - - - - - - rs1953696 13:100805582 T 5095 NM_001178004.1 Transcript intron_variant - - - - - - rs1953696 13:100805582 T 5095 NM_000282.3 Transcript intron_variant - - - - - - rs1953696 13:100805582 T 5095 NM_001127692.2 Transcript intron_variant - - - - - - rs1953696 13:100805582 T ENSESTG00000026853 ENSESTT00000068166 Transcript intron_variant - - - - - - rs1953696 13:100805582 T ENSESTG00000026853 ENSESTT00000068191 Transcript intron_variant - - - - - - rs1953696 13:100805582 T CCDS53878.1 CCDS53878.1 Transcript intron_variant - - - - - - rs2256147 13:101612695 A 100885778 NR_047687.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7997212 13:101625985 G 100885778 NR_047687.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2765300 13:101653394 C 100885778 NR_047687.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2390577 13:101892631 T 259232 NM_052867.2 Transcript intron_variant - - - - - - rs2390577 13:101892631 T CCDS9498.1 CCDS9498.1 Transcript intron_variant - - - - - - rs2390577 13:101892631 T ENSESTG00000016422 ENSESTT00000041222 Transcript intron_variant - - - - - - rs9300657 13:101905821 A 259232 NM_052867.2 Transcript intron_variant - - - - - - rs9300657 13:101905821 A CCDS9498.1 CCDS9498.1 Transcript intron_variant - - - - - - rs9300657 13:101905821 A ENSESTG00000016422 ENSESTT00000041222 Transcript intron_variant - - - - - - rs540560 13:101983159 G 259232 NM_052867.2 Transcript intron_variant - - - - - - rs540560 13:101983159 G ENSESTG00000016422 ENSESTT00000041231 Transcript intron_variant - - - - - - rs540560 13:101983159 G CCDS9498.1 CCDS9498.1 Transcript intron_variant - - - - - - rs540560 13:101983159 G ENSESTG00000016422 ENSESTT00000041222 Transcript intron_variant - - - - - - rs1572323 13:102096908 C - - - intergenic_variant - - - - - - rs1932266 13:102210076 T ENSESTG00000016373 ENSESTT00000041145 Transcript intron_variant - - - - - - rs1932266 13:102210076 T CCDS9499.1 CCDS9499.1 Transcript intron_variant - - - - - - rs1932266 13:102210076 T ENSESTG00000016373 ENSESTT00000041140 Transcript intron_variant - - - - - - rs1932266 13:102210076 T ENSESTG00000016373 ENSESTT00000041101 Transcript intron_variant - - - - - - rs1932266 13:102210076 T 9358 NM_004791.1 Transcript intron_variant - - - - - - rs1932266 13:102210076 T ENSESTG00000016373 ENSESTT00000041135 Transcript intron_variant - - - - - - rs1932266 13:102210076 T ENSESTG00000016373 ENSESTT00000041130 Transcript intron_variant - - - - - - rs1927713 13:102423142 C 2259 NM_004115.3 Transcript intron_variant - - - - - - rs1927713 13:102423142 C CCDS9500.1 CCDS9500.1 Transcript intron_variant - - - - - - rs1927713 13:102423142 C CCDS9501.1 CCDS9501.1 Transcript intron_variant - - - - - - rs1927713 13:102423142 C ENSESTG00000005576 ENSESTT00000014182 Transcript intron_variant - - - - - - rs1927713 13:102423142 C 2259 NM_175929.2 Transcript intron_variant - - - - - - rs4381455 13:102469118 G 2259 NM_004115.3 Transcript intron_variant - - - - - - rs4381455 13:102469118 G CCDS9500.1 CCDS9500.1 Transcript intron_variant - - - - - - rs4381455 13:102469118 G CCDS9501.1 CCDS9501.1 Transcript intron_variant - - - - - - rs4381455 13:102469118 G ENSESTG00000005576 ENSESTT00000014182 Transcript intron_variant - - - - - - rs4381455 13:102469118 G 2259 NM_175929.2 Transcript intron_variant - - - - - - rs4328306 13:103039422 T ENSESTG00000005568 ENSESTT00000014150 Transcript intron_variant - - - - - - rs4328306 13:103039422 T CCDS9500.1 CCDS9500.1 Transcript intron_variant - - - - - - rs4328306 13:103039422 T ENSESTG00000005568 ENSESTT00000014155 Transcript intron_variant - - - - - - rs4328306 13:103039422 T 283480 NR_036486.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4328306 13:103039422 T 2259 NM_175929.2 Transcript intron_variant - - - - - - rs4328306 13:103039422 T ENSESTG00000005568 ENSESTT00000014153 Transcript intron_variant - - - - - - rs2094257 13:103434365 T CCDS9504.1 CCDS9504.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2480 rs2094257 13:103434365 T ENSESTG00000028106 ENSESTT00000070853 Transcript downstream_gene_variant - - - - - - DISTANCE=2269 rs2094257 13:103434365 T ENSESTG00000028106 ENSESTT00000070805 Transcript downstream_gene_variant - - - - - - DISTANCE=2267 rs2094257 13:103434365 T 79070 NM_024089.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2266 rs2094257 13:103434365 T ENSESTG00000028106 ENSESTT00000070838 Transcript downstream_gene_variant - - - - - - DISTANCE=2269 rs4772501 13:103449686 C CCDS9504.1 CCDS9504.1 Transcript intron_variant - - - - - - rs4772501 13:103449686 C ENSESTG00000027830 ENSESTT00000070234 Transcript upstream_gene_variant - - - - - - DISTANCE=2830 rs4772501 13:103449686 C ENSESTG00000027830 ENSESTT00000070216 Transcript upstream_gene_variant - - - - - - DISTANCE=2003 rs4772501 13:103449686 C ENSESTG00000027830 ENSESTT00000070145 Transcript upstream_gene_variant - - - - - - DISTANCE=2003 rs4772501 13:103449686 C 54841 NM_001159596.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1713 rs4772501 13:103449686 C 54841 NM_017693.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1713 rs4772501 13:103449686 C ENSESTG00000027830 ENSESTT00000070085 Transcript upstream_gene_variant - - - - - - DISTANCE=1788 rs4772501 13:103449686 C ENSESTG00000028106 ENSESTT00000070805 Transcript intron_variant - - - - - - rs4772501 13:103449686 C ENSESTG00000027830 ENSESTT00000070041 Transcript upstream_gene_variant - - - - - - DISTANCE=1783 rs4772501 13:103449686 C 79070 NM_024089.2 Transcript intron_variant - - - - - - rs1323699 13:103512927 A ENSESTG00000027921 ENSESTT00000070372 Transcript intron_variant - - - - - - rs1323699 13:103512927 A 100533467 NM_001204425.1 Transcript intron_variant - - - - - - rs1323699 13:103512927 A ENSESTG00000027921 ENSESTT00000070429 Transcript intron_variant - - - - - - rs1323699 13:103512927 A 2073 NM_000123.3 Transcript intron_variant - - - - - - rs1323699 13:103512927 A ENSESTG00000027921 ENSESTT00000070359 Transcript intron_variant - - - - - - rs1323699 13:103512927 A ENSESTG00000027921 ENSESTT00000070416 Transcript intron_variant - - - - - - rs1323699 13:103512927 A ENSESTG00000027997 ENSESTT00000070593 Transcript upstream_gene_variant - - - - - - DISTANCE=2035 rs1323699 13:103512927 A CCDS32004.1 CCDS32004.1 Transcript intron_variant - - - - - - rs4771437 13:103517642 G ENSESTG00000027921 ENSESTT00000070372 Transcript downstream_gene_variant - - - - - - DISTANCE=3568 rs4771437 13:103517642 G 100533467 NM_001204425.1 Transcript intron_variant - - - - - - rs4771437 13:103517642 G ENSESTG00000027921 ENSESTT00000070429 Transcript downstream_gene_variant - - - - - - DISTANCE=3568 rs4771437 13:103517642 G 2073 NM_000123.3 Transcript intron_variant - - - - - - rs4771437 13:103517642 G ENSESTG00000027921 ENSESTT00000070359 Transcript downstream_gene_variant - - - - - - DISTANCE=2979 rs4771437 13:103517642 G ENSESTG00000027921 ENSESTT00000070416 Transcript downstream_gene_variant - - - - - - DISTANCE=2979 rs4771437 13:103517642 G ENSESTG00000027997 ENSESTT00000070593 Transcript intron_variant - - - - - - rs4771437 13:103517642 G CCDS32004.1 CCDS32004.1 Transcript intron_variant - - - - - - rs4771438 13:103523238 G - ENSR00001511955 RegulatoryFeature regulatory_region_variant - - - - - - rs4771438 13:103523238 G 100533467 NM_001204425.1 Transcript intron_variant - - - - - - rs4771438 13:103523238 G 2073 NM_000123.3 Transcript intron_variant - - - - - - rs4771438 13:103523238 G ENSESTG00000027997 ENSESTT00000070593 Transcript intron_variant - - - - - - rs4771438 13:103523238 G CCDS32004.1 CCDS32004.1 Transcript intron_variant - - - - - - rs7984530 13:103526662 A 100533467 NM_001204425.1 Transcript intron_variant - - - - - - rs7984530 13:103526662 A 2073 NM_000123.3 Transcript intron_variant - - - - - - rs7984530 13:103526662 A ENSESTG00000027997 ENSESTT00000070593 Transcript intron_variant - - - - - - rs7984530 13:103526662 A CCDS32004.1 CCDS32004.1 Transcript intron_variant - - - - - - rs943248 13:103531667 C 100533467 NM_001204425.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3316 rs943248 13:103531667 C ENSESTG00000028077 ENSESTT00000070613 Transcript upstream_gene_variant - - - - - - DISTANCE=782 rs943248 13:103531667 C 2073 NM_000123.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3316 rs943248 13:103531667 C ENSESTG00000027997 ENSESTT00000070593 Transcript downstream_gene_variant - - - - - - DISTANCE=3760 rs943248 13:103531667 C 121952 NR_026965.1 Transcript upstream_gene_variant - - - - - - DISTANCE=782 rs943248 13:103531667 C CCDS32004.1 CCDS32004.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3414 rs2699358 13:103849258 G - - - intergenic_variant - - - - - - rs3005623 13:103923864 G - - - intergenic_variant - - - - - - rs4772569 13:104253239 C - - - intergenic_variant - - - - - - rs4772580 13:104318836 T - - - intergenic_variant - - - - - - rs1849453 13:104732325 G - - - intergenic_variant - - - - - - rs9519386 13:105227857 C - - - intergenic_variant - - - - - - rs796602 13:106196770 A - - - intergenic_variant - - - - - - rs1328093 13:106427787 A - - - intergenic_variant - - - - - - rs7995374 13:106428099 A - - - intergenic_variant - - - - - - rs1550604 13:106794125 C - - - intergenic_variant - - - - - - rs354416 13:106902843 A - - - intergenic_variant - - - - - - rs353774 13:106994256 G - - - intergenic_variant - - - - - - rs7995379 13:107145463 C ENSESTG00000022916 ENSESTT00000057825 Transcript splice_region_variant,intron_variant - - - - - - rs7995379 13:107145463 C 1948 NM_004093.3 Transcript synonymous_variant 1003 927 309 G ggC/ggG - rs7995379 13:107145463 C CCDS9507.1 CCDS9507.1 Transcript synonymous_variant 927 927 309 G ggC/ggG - rs9520128 13:107277768 A ENSESTG00000022889 ENSESTT00000057687 Transcript intron_variant - - - - - - rs9520128 13:107277768 A 283483 NR_051977.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4772809 13:107357080 T - - - intergenic_variant - - - - - - rs425015 13:107427579 C - - - intergenic_variant - - - - - - rs287211 13:107437950 G - - - intergenic_variant - - - - - - rs2806515 13:107812799 G - - - intergenic_variant - - - - - - rs1018724 13:108792245 C - - - intergenic_variant - - - - - - rs2391622 13:108811442 C - - - intergenic_variant - - - - - - rs1326411 13:109012914 G - - - intergenic_variant - - - - - - rs149729 13:109400699 A ENSESTG00000003766 ENSESTT00000009479 Transcript intron_variant - - - - - - rs149729 13:109400699 A 23026 NM_015011.1 Transcript intron_variant - - - - - - rs149729 13:109400699 A CCDS32008.1 CCDS32008.1 Transcript intron_variant - - - - - - rs149729 13:109400699 A 23026 NM_001198950.1 Transcript intron_variant - - - - - - rs7991917 13:109549721 A - ENSR00001512181 RegulatoryFeature regulatory_region_variant - - - - - - rs7991917 13:109549721 A ENSESTG00000029112 ENSESTT00000073303 Transcript intron_variant - - - - - - rs7991917 13:109549721 A 23026 NM_015011.1 Transcript intron_variant - - - - - - rs7991917 13:109549721 A CCDS32008.1 CCDS32008.1 Transcript intron_variant - - - - - - rs7991917 13:109549721 A 23026 NM_001198950.1 Transcript intron_variant - - - - - - rs7317429 13:109556586 C 23026 NM_015011.1 Transcript intron_variant - - - - - - rs7317429 13:109556586 C CCDS32008.1 CCDS32008.1 Transcript intron_variant - - - - - - rs7317429 13:109556586 C 23026 NM_001198950.1 Transcript intron_variant - - - - - - rs644335 13:109814768 C - ENSR00000520371 RegulatoryFeature regulatory_region_variant - - - - - - rs644335 13:109814768 C 100885782 NR_047700.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1485 rs644335 13:109814768 C ENSESTG00000029214 ENSESTT00000073593 Transcript intron_variant - - - - - - rs644335 13:109814768 C 23026 NM_015011.1 Transcript intron_variant - - - - - - rs644335 13:109814768 C CCDS32008.1 CCDS32008.1 Transcript intron_variant - - - - - - rs644335 13:109814768 C 23026 NM_001198950.1 Transcript intron_variant - - - - - - rs496081 13:109817127 A 100885782 NR_047700.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs496081 13:109817127 A ENSESTG00000029214 ENSESTT00000073593 Transcript intron_variant - - - - - - rs496081 13:109817127 A 23026 NM_015011.1 Transcript intron_variant - - - - - - rs496081 13:109817127 A CCDS32008.1 CCDS32008.1 Transcript intron_variant - - - - - - rs496081 13:109817127 A 23026 NM_001198950.1 Transcript intron_variant - - - - - - rs1328940 13:109821082 A 100885782 NR_047700.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1431 rs1328940 13:109821082 A ENSESTG00000029214 ENSESTT00000073593 Transcript intron_variant - - - - - - rs1328940 13:109821082 A 23026 NM_015011.1 Transcript intron_variant - - - - - - rs1328940 13:109821082 A CCDS32008.1 CCDS32008.1 Transcript intron_variant - - - - - - rs1328940 13:109821082 A 23026 NM_001198950.1 Transcript intron_variant - - - - - - rs609726 13:109826463 A ENSESTG00000029214 ENSESTT00000073593 Transcript intron_variant - - - - - - rs609726 13:109826463 A 23026 NM_015011.1 Transcript intron_variant - - - - - - rs609726 13:109826463 A CCDS32008.1 CCDS32008.1 Transcript intron_variant - - - - - - rs609726 13:109826463 A 23026 NM_001198950.1 Transcript intron_variant - - - - - - rs2149516 13:109827581 G ENSESTG00000029214 ENSESTT00000073593 Transcript intron_variant - - - - - - rs2149516 13:109827581 G 23026 NM_015011.1 Transcript intron_variant - - - - - - rs2149516 13:109827581 G CCDS32008.1 CCDS32008.1 Transcript intron_variant - - - - - - rs2149516 13:109827581 G 23026 NM_001198950.1 Transcript intron_variant - - - - - - rs641754 13:109889576 C ENSESTG00000029243 ENSESTT00000073652 Transcript intron_variant - - - - - - rs4773052 13:110128490 T - - - intergenic_variant - - - - - - rs6492200 13:110136668 G - - - intergenic_variant - - - - - - rs1571747 13:110215139 T - - - intergenic_variant - - - - - - rs928542 13:110598507 G - - - intergenic_variant - - - - - - rs7321455 13:110670309 C - - - intergenic_variant - - - - - - rs1543734 13:110675616 G - - - intergenic_variant - - - - - - rs4773113 13:110683091 T - - - intergenic_variant - - - - - - rs472457 13:110832466 C ENSESTG00000018614 ENSESTT00000046931 Transcript intron_variant - - - - - - rs472457 13:110832466 C ENSESTG00000018614 ENSESTT00000046945 Transcript intron_variant - - - - - - rs472457 13:110832466 C 1282 NM_001845.4 Transcript intron_variant - - - - - - rs472457 13:110832466 C CCDS9511.1 CCDS9511.1 Transcript intron_variant - - - - - - rs536174 13:110839550 G ENSESTG00000018614 ENSESTT00000046931 Transcript missense_variant 185 4 2 T/P Aca/Cca - rs536174 13:110839550 G ENSESTG00000018614 ENSESTT00000046945 Transcript missense_variant 185 4 2 T/P Aca/Cca - rs536174 13:110839550 G 1282 NM_001845.4 Transcript missense_variant 1785 1663 555 T/P Aca/Cca - PolyPhen=unknown;SIFT=tolerated rs536174 13:110839550 G CCDS9511.1 CCDS9511.1 Transcript missense_variant 1663 1663 555 T/P Aca/Cca - PolyPhen=unknown;SIFT=tolerated rs619197 13:110884222 C ENSESTG00000018504 ENSESTT00000046791 Transcript intron_variant - - - - - - rs619197 13:110884222 C ENSESTG00000018504 ENSESTT00000046779 Transcript intron_variant - - - - - - rs619197 13:110884222 C ENSESTG00000018504 ENSESTT00000046705 Transcript intron_variant - - - - - - rs619197 13:110884222 C 1282 NM_001845.4 Transcript intron_variant - - - - - - rs619197 13:110884222 C CCDS9511.1 CCDS9511.1 Transcript intron_variant - - - - - - rs619197 13:110884222 C ENSESTG00000018504 ENSESTT00000046807 Transcript intron_variant - - - - - - rs619197 13:110884222 C ENSESTG00000018504 ENSESTT00000046798 Transcript intron_variant - - - - - - rs693358 13:110885832 A - ENSR00000520518 RegulatoryFeature regulatory_region_variant - - - - - - rs693358 13:110885832 A ENSESTG00000018504 ENSESTT00000046791 Transcript intron_variant - - - - - - rs693358 13:110885832 A ENSESTG00000018504 ENSESTT00000046779 Transcript intron_variant - - - - - - rs693358 13:110885832 A ENSESTG00000018504 ENSESTT00000046705 Transcript intron_variant - - - - - - rs693358 13:110885832 A 1282 NM_001845.4 Transcript intron_variant - - - - - - rs693358 13:110885832 A CCDS9511.1 CCDS9511.1 Transcript intron_variant - - - - - - rs693358 13:110885832 A ENSESTG00000018504 ENSESTT00000046807 Transcript intron_variant - - - - - - rs693358 13:110885832 A ENSESTG00000018504 ENSESTT00000046798 Transcript intron_variant - - - - - - rs611586 13:110937372 A ENSESTG00000018504 ENSESTT00000046791 Transcript intron_variant - - - - - - rs611586 13:110937372 A ENSESTG00000018504 ENSESTT00000046779 Transcript intron_variant - - - - - - rs611586 13:110937372 A ENSESTG00000018504 ENSESTT00000046705 Transcript intron_variant - - - - - - rs611586 13:110937372 A 1282 NM_001845.4 Transcript intron_variant - - - - - - rs611586 13:110937372 A CCDS9511.1 CCDS9511.1 Transcript intron_variant - - - - - - rs611586 13:110937372 A ENSESTG00000018504 ENSESTT00000046807 Transcript intron_variant - - - - - - rs611586 13:110937372 A ENSESTG00000018504 ENSESTT00000046798 Transcript intron_variant - - - - - - rs6492254 13:110949553 C ENSESTG00000018504 ENSESTT00000046791 Transcript intron_variant - - - - - - rs6492254 13:110949553 C ENSESTG00000018504 ENSESTT00000046779 Transcript intron_variant - - - - - - rs6492254 13:110949553 C ENSESTG00000018504 ENSESTT00000046705 Transcript intron_variant - - - - - - rs6492254 13:110949553 C 1282 NM_001845.4 Transcript intron_variant - - - - - - rs6492254 13:110949553 C CCDS9511.1 CCDS9511.1 Transcript intron_variant - - - - - - rs6492254 13:110949553 C ENSESTG00000018504 ENSESTT00000046807 Transcript intron_variant - - - - - - rs6492254 13:110949553 C ENSESTG00000018504 ENSESTT00000046798 Transcript intron_variant - - - - - - rs4450261 13:111128594 C CCDS41907.1 CCDS41907.1 Transcript intron_variant - - - - - - rs4450261 13:111128594 C 1284 NM_001846.2 Transcript intron_variant - - - - - - rs4450261 13:111128594 C ENSESTG00000017868 ENSESTT00000045789 Transcript intron_variant - - - - - - rs4450261 13:111128594 C ENSESTG00000017868 ENSESTT00000045816 Transcript intron_variant - - - - - - rs4450261 13:111128594 C ENSESTG00000017868 ENSESTT00000045717 Transcript intron_variant - - - - - - rs1983930 13:111137167 C CCDS41907.1 CCDS41907.1 Transcript intron_variant - - - - - - rs1983930 13:111137167 C 1284 NM_001846.2 Transcript intron_variant - - - - - - rs1983930 13:111137167 C ENSESTG00000017868 ENSESTT00000045789 Transcript intron_variant - - - - - - rs1983930 13:111137167 C ENSESTG00000017868 ENSESTT00000045816 Transcript intron_variant - - - - - - rs1983930 13:111137167 C ENSESTG00000018488 ENSESTT00000046543 Transcript downstream_gene_variant - - - - - - DISTANCE=98 rs1983930 13:111137167 C ENSESTG00000017868 ENSESTT00000045717 Transcript intron_variant - - - - - - rs390183 13:111221571 G - - - intergenic_variant - - - - - - rs2391846 13:111253061 G - - - intergenic_variant - - - - - - rs7338333 13:111368164 G - ENSR00000520638 RegulatoryFeature regulatory_region_variant - - - - - - rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012124 Transcript upstream_gene_variant - - - - - - DISTANCE=2302 rs7338333 13:111368164 G CCDS9518.1 CCDS9518.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3483 rs7338333 13:111368164 G 3621 NM_005537.4 Transcript missense_variant 806 374 125 L/R cTg/cGg - PolyPhen=benign;SIFT=tolerated rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012121 Transcript upstream_gene_variant - - - - - - DISTANCE=2302 rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012105 Transcript upstream_gene_variant - - - - - - DISTANCE=2216 rs7338333 13:111368164 G CCDS9516.1 CCDS9516.1 Transcript intron_variant - - - - - - rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012127 Transcript upstream_gene_variant - - - - - - DISTANCE=2314 rs7338333 13:111368164 G CCDS9515.1 CCDS9515.1 Transcript intron_variant - - - - - - rs7338333 13:111368164 G 3621 NM_198217.2 Transcript intron_variant - - - - - - rs7338333 13:111368164 G ENSESTG00000009478 ENSESTT00000023741 Transcript intron_variant - - - - - - rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012132 Transcript upstream_gene_variant - - - - - - DISTANCE=3329 rs7338333 13:111368164 G 3621 NM_198218.2 Transcript intron_variant - - - - - - rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012131 Transcript upstream_gene_variant - - - - - - DISTANCE=3329 rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012117 Transcript upstream_gene_variant - - - - - - DISTANCE=2216 rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012114 Transcript upstream_gene_variant - - - - - - DISTANCE=2216 rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012130 Transcript upstream_gene_variant - - - - - - DISTANCE=2314 rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012133 Transcript upstream_gene_variant - - - - - - DISTANCE=3329 rs7338333 13:111368164 G ENSESTG00000009478 ENSESTT00000023736 Transcript intron_variant - - - - - - rs7338333 13:111368164 G ENSESTG00000004761 ENSESTT00000012126 Transcript upstream_gene_variant - - - - - - DISTANCE=2314 rs7338333 13:111368164 G CCDS9517.1 CCDS9517.1 Transcript missense_variant 374 374 125 L/R cTg/cGg - PolyPhen=benign;SIFT=tolerated rs7338333 13:111368164 G ENSESTG00000009478 ENSESTT00000023749 Transcript upstream_gene_variant - - - - - - DISTANCE=26 rs7338333 13:111368164 G 3621 NM_198219.2 Transcript intron_variant - - - - - - rs7338333 13:111368164 G 3621 NM_001267728.1 Transcript intron_variant - - - - - - rs2766713 13:111407947 T - - - intergenic_variant - - - - - - rs191289 13:111456417 C - - - intergenic_variant - - - - - - rs1164269 13:111858103 C 8874 NM_003899.3 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023985 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023954 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023951 Transcript intron_variant - - - - - - rs1164269 13:111858103 C CCDS45068.1 CCDS45068.1 Transcript intron_variant - - - - - - rs1164269 13:111858103 C 8874 NM_001113511.1 Transcript intron_variant - - - - - - rs1164269 13:111858103 C 8874 NM_145735.2 Transcript intron_variant - - - - - - rs1164269 13:111858103 C CCDS32009.1 CCDS32009.1 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023986 Transcript intron_variant - - - - - - rs1164269 13:111858103 C CCDS45069.1 CCDS45069.1 Transcript intron_variant - - - - - - rs1164269 13:111858103 C 8874 NM_001113512.1 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000024002 Transcript upstream_gene_variant - - - - - - DISTANCE=4040 rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000024004 Transcript upstream_gene_variant - - - - - - DISTANCE=4040 rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023884 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023886 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023966 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023996 Transcript upstream_gene_variant - - - - - - DISTANCE=4040 rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023896 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023989 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023997 Transcript upstream_gene_variant - - - - - - DISTANCE=4040 rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023907 Transcript intron_variant - - - - - - rs1164269 13:111858103 C 8874 NM_001113513.1 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023901 Transcript downstream_gene_variant - - - - - - DISTANCE=247 rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023971 Transcript intron_variant - - - - - - rs1164269 13:111858103 C ENSESTG00000009526 ENSESTT00000023991 Transcript intron_variant - - - - - - rs942654 13:111928607 T 8874 NM_003899.3 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023985 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023954 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023951 Transcript intron_variant - - - - - - rs942654 13:111928607 T CCDS45068.1 CCDS45068.1 Transcript intron_variant - - - - - - rs942654 13:111928607 T 8874 NM_001113511.1 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000024015 Transcript intron_variant - - - - - - rs942654 13:111928607 T 8874 NM_145735.2 Transcript intron_variant - - - - - - rs942654 13:111928607 T CCDS32009.1 CCDS32009.1 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023986 Transcript intron_variant - - - - - - rs942654 13:111928607 T CCDS45069.1 CCDS45069.1 Transcript intron_variant - - - - - - rs942654 13:111928607 T 8874 NM_001113512.1 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000024002 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000024004 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023966 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023996 Transcript intron_variant - - - - - - rs942654 13:111928607 T CCDS9521.1 CCDS9521.1 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000024020 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023989 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023997 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000024019 Transcript intron_variant - - - - - - rs942654 13:111928607 T 8874 NM_001113513.1 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023991 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000023971 Transcript intron_variant - - - - - - rs942654 13:111928607 T ENSESTG00000009526 ENSESTT00000024009 Transcript intron_variant - - - - - - rs1886559 13:111930961 A 8874 NM_003899.3 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023985 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023954 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023951 Transcript intron_variant - - - - - - rs1886559 13:111930961 A CCDS45068.1 CCDS45068.1 Transcript intron_variant - - - - - - rs1886559 13:111930961 A 8874 NM_001113511.1 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000024015 Transcript intron_variant - - - - - - rs1886559 13:111930961 A 8874 NM_145735.2 Transcript intron_variant - - - - - - rs1886559 13:111930961 A CCDS32009.1 CCDS32009.1 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023986 Transcript intron_variant - - - - - - rs1886559 13:111930961 A CCDS45069.1 CCDS45069.1 Transcript intron_variant - - - - - - rs1886559 13:111930961 A 8874 NM_001113512.1 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000024002 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000024004 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023966 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023996 Transcript intron_variant - - - - - - rs1886559 13:111930961 A CCDS9521.1 CCDS9521.1 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000024020 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023989 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023997 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000024019 Transcript intron_variant - - - - - - rs1886559 13:111930961 A 8874 NM_001113513.1 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023991 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000023971 Transcript intron_variant - - - - - - rs1886559 13:111930961 A ENSESTG00000009526 ENSESTT00000024009 Transcript intron_variant - - - - - - rs2528769 13:112074033 C - - - intergenic_variant - - - - - - rs943901 13:112074177 G - - - intergenic_variant - - - - - - rs1028975 13:112074965 T - - - intergenic_variant - - - - - - rs2774428 13:112076359 G - - - intergenic_variant - - - - - - rs1341155 13:112326822 G ENSESTG00000025628 ENSESTT00000064652 Transcript downstream_gene_variant - - - - - - DISTANCE=1872 rs7995689 13:112808262 G - - - intergenic_variant - - - - - - rs2149213 13:113106745 G - - - intergenic_variant - - - - - - rs382100 13:113351992 C CCDS32011.1 CCDS32011.1 Transcript intron_variant - - - - - - rs382100 13:113351992 C 23250 NM_015205.2 Transcript intron_variant - - - - - - rs382100 13:113351992 C ENSESTG00000030496 ENSESTT00000076857 Transcript intron_variant - - - - - - rs382100 13:113351992 C ENSESTG00000031487 ENSESTT00000079429 Transcript intron_variant - - - - - - rs382100 13:113351992 C 23250 NM_032189.3 Transcript intron_variant - - - - - - rs380069 13:113367147 C CCDS32011.1 CCDS32011.1 Transcript intron_variant - - - - - - rs380069 13:113367147 C 23250 NM_015205.2 Transcript intron_variant - - - - - - rs380069 13:113367147 C ENSESTG00000030496 ENSESTT00000076857 Transcript intron_variant - - - - - - rs380069 13:113367147 C ENSESTG00000031487 ENSESTT00000079429 Transcript intron_variant - - - - - - rs380069 13:113367147 C 23250 NM_032189.3 Transcript intron_variant - - - - - - rs1278767 13:113534484 C ENSESTG00000030578 ENSESTT00000077006 Transcript intron_variant - - - - - - rs1278767 13:113534484 C CCDS32011.1 CCDS32011.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1876 rs1278767 13:113534484 C 23250 NM_015205.2 Transcript intron_variant - - - - - - rs1278767 13:113534484 C ENSESTG00000031487 ENSESTT00000079429 Transcript intron_variant - - - - - - rs1278767 13:113534484 C ENSESTG00000030578 ENSESTT00000077017 Transcript downstream_gene_variant - - - - - - DISTANCE=4076 rs1278767 13:113534484 C ENSESTG00000030578 ENSESTT00000077028 Transcript upstream_gene_variant - - - - - - DISTANCE=131 rs1278767 13:113534484 C 23250 NM_032189.3 Transcript intron_variant - - - - - - rs796564 13:113824136 C - ENSR00000520924 RegulatoryFeature regulatory_region_variant - - - - - - rs796564 13:113824136 C ENSESTG00000030881 ENSESTT00000077840 Transcript upstream_gene_variant - - - - - - DISTANCE=584 rs796564 13:113824136 C ENSESTG00000030881 ENSESTT00000077798 Transcript intron_variant - - - - - - rs796564 13:113824136 C 8858 NM_003891.2 Transcript intron_variant - - - - - - rs796564 13:113824136 C CCDS9531.1 CCDS9531.1 Transcript intron_variant - - - - - - rs796564 13:113824136 C 8858 NM_001256134.1 Transcript intron_variant - - - - - - rs796564 13:113824136 C ENSESTG00000030881 ENSESTT00000077830 Transcript intron_variant - - - - - - rs796564 13:113824136 C CCDS58300.1 CCDS58300.1 Transcript intron_variant - - - - - - rs4907615 13:114002382 C - ENSR00001512543 RegulatoryFeature regulatory_region_variant - - - - - - rs4907615 13:114002382 C ENSESTG00000031328 ENSESTT00000079059 Transcript intron_variant - - - - - - rs4907615 13:114002382 C ENSESTG00000031118 ENSESTT00000078358 Transcript upstream_gene_variant - - - - - - DISTANCE=3756 rs4907615 13:114002382 C CCDS9534.2 CCDS9534.2 Transcript intron_variant - - - - - - rs4907615 13:114002382 C ENSESTG00000031328 ENSESTT00000079011 Transcript intron_variant - - - - - - rs4907615 13:114002382 C 79774 NM_024719.2 Transcript intron_variant - - - - - - rs4907615 13:114002382 C ENSESTG00000031328 ENSESTT00000079043 Transcript intron_variant - - - - - - rs4907615 13:114002382 C ENSESTG00000031118 ENSESTT00000078352 Transcript upstream_gene_variant - - - - - - DISTANCE=3606 rs7326569 13:114100629 G - ENSR00001036792 RegulatoryFeature regulatory_region_variant - - - - - - rs7326569 13:114100629 G ENSESTG00000031286 ENSESTT00000078922 Transcript intron_variant - - - - - - rs7326569 13:114100629 G ENSESTG00000031286 ENSESTT00000078983 Transcript upstream_gene_variant - - - - - - DISTANCE=1747 rs7326569 13:114100629 G 113622 NM_199162.1 Transcript intron_variant - - - - - - rs7326569 13:114100629 G ENSESTG00000031286 ENSESTT00000078968 Transcript intron_variant - - - - - - rs7326569 13:114100629 G CCDS9536.1 CCDS9536.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1757 rs7326569 13:114100629 G ENSESTG00000031286 ENSESTT00000078941 Transcript intron_variant - - - - - - rs7326569 13:114100629 G 113622 NM_138430.3 Transcript intron_variant - - - - - - rs7326569 13:114100629 G CCDS9535.1 CCDS9535.1 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078720 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031250 ENSESTT00000078775 Transcript downstream_gene_variant - - - - - - DISTANCE=3689 rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078734 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078707 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078691 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078617 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078718 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078599 Transcript intron_variant - - - - - - rs2265144 13:114177835 A 55002 NM_017905.4 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078658 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078743 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078653 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078748 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078723 Transcript intron_variant - - - - - - rs2265144 13:114177835 A CCDS9537.1 CCDS9537.1 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078607 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078548 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078632 Transcript intron_variant - - - - - - rs2265144 13:114177835 A ENSESTG00000031152 ENSESTT00000078577 Transcript intron_variant - - - - - - rs9285616 13:114312354 G CCDS9539.1 CCDS9539.1 Transcript synonymous_variant 106 106 36 R Agg/Cgg - rs9285616 13:114312354 G ENSESTG00000019164 ENSESTT00000048201 Transcript synonymous_variant 148 106 36 R Agg/Cgg - rs9285616 13:114312354 G 496 NM_000705.3 Transcript synonymous_variant 160 106 36 R Agg/Cgg - rs9285616 13:114312354 G ENSESTG00000019164 ENSESTT00000048230 Transcript intron_variant - - - - - - rs6602898 13:114612080 G - ENSR00000521069 RegulatoryFeature regulatory_region_variant - - - - - - rs6602898 13:114612080 G ENSESTG00000018328 ENSESTT00000046144 Transcript intron_variant - - - - - - rs61972026 13:114919040 A - - - intergenic_variant - - - - - - rs12147376 14:20217342 A 441669 NM_172194.1 Transcript downstream_gene_variant - - - - - - DISTANCE=814 rs12147376 14:20217342 A CCDS32020.1 CCDS32020.1 Transcript downstream_gene_variant - - - - - - DISTANCE=814 rs12147376 14:20217342 A ENSESTG00000029727 ENSESTT00000074790 Transcript intron_variant - - - - - - rs2932229 14:20257258 T ENSESTG00000029727 ENSESTT00000074790 Transcript intron_variant - - - - - - rs2635541 14:20263752 T ENSESTG00000029727 ENSESTT00000074790 Transcript intron_variant - - - - - - rs1686613 14:20310712 A - - - intergenic_variant - - - - - - rs2105261 14:20500015 A CCDS32028.1 CCDS32028.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1988 rs2105261 14:20500015 A 390433 NM_001004714.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1988 rs1243688 14:21062097 T 493901 NM_001024822.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3115 rs1243688 14:21062097 T 122651 NM_145250.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3680 rs1243688 14:21062097 T ENSESTG00000023711 ENSESTT00000059797 Transcript intron_variant - - - - - - rs1243688 14:21062097 T ENSESTG00000022636 ENSESTT00000057132 Transcript intron_variant - - - - - - rs1243688 14:21062097 T CCDS32037.1 CCDS32037.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3215 rs1243688 14:21062097 T ENSESTG00000023711 ENSESTT00000059790 Transcript intron_variant - - - - - - rs1243688 14:21062097 T ENSESTG00000022636 ENSESTT00000057117 Transcript downstream_gene_variant - - - - - - DISTANCE=3680 rs7155477 14:21166752 T ENSESTG00000022655 ENSESTT00000057200 Transcript downstream_gene_variant - - - - - - DISTANCE=4412 rs7155477 14:21166752 T ENSESTG00000023701 ENSESTT00000059753 Transcript intron_variant - - - - - - rs7155477 14:21166752 T 6038 NM_194431.1 Transcript intron_variant - - - - - - rs7155477 14:21166752 T ENSESTG00000022655 ENSESTT00000057176 Transcript downstream_gene_variant - - - - - - DISTANCE=4412 rs7155477 14:21166752 T CCDS9555.1 CCDS9555.1 Transcript upstream_gene_variant - - - - - - DISTANCE=779 rs7155477 14:21166752 T 283 NM_001145.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4407 rs7155477 14:21166752 T 283 NM_001097577.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4407 rs7155477 14:21166752 T ENSESTG00000022655 ENSESTT00000057190 Transcript downstream_gene_variant - - - - - - DISTANCE=4412 rs7155477 14:21166752 T 6038 NM_002937.3 Transcript intron_variant - - - - - - rs7155477 14:21166752 T CCDS9554.1 CCDS9554.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4585 rs2873981 14:21278615 G - - - intergenic_variant - - - - - - rs7152476 14:21285380 C - ENSR00000414939 RegulatoryFeature regulatory_region_variant - - - - - - rs7152476 14:21285380 C - PB0058.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_NAME=Jaspar_Matrix_PU1:PB0058.1;HIGH_INF_POS=N rs7152476 14:21285380 C - - - intergenic_variant - - - - - - rs4982379 14:21377226 T ENSESTG00000023695 ENSESTT00000059730 Transcript intron_variant - - - - - - rs1263818 14:22019991 A - - - intergenic_variant - - - - - - rs4982484 14:22151666 A - - - intergenic_variant - - - - - - rs6572018 14:22167296 C - - - intergenic_variant - - - - - - rs8005757 14:22183862 T ENSESTG00000026464 ENSESTT00000066649 Transcript intron_variant - - - - - - rs8005757 14:22183862 T 28691 NC_000014.8:TRAV2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2796 rs8005757 14:22183862 T ENSESTG00000026449 ENSESTT00000066642 Transcript downstream_gene_variant - - - - - - DISTANCE=2418 rs1304855 14:22211657 A ENSESTG00000026473 ENSESTT00000066681 Transcript intron_variant - - - - - - rs6572101 14:22283968 A 28678 NC_000014.8:TRAV9-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3819 rs10138370 14:22285246 C - - - intergenic_variant - - - - - - rs2178782 14:22293510 C - ENSR00001455882 RegulatoryFeature regulatory_region_variant - - - - - - rs2178782 14:22293510 C 28676 NC_000014.8:TRAV10:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=162 rs2178782 14:22293510 C 28675 NC_000014.8:TRAV11:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4182 rs2204954 14:22299150 A 28676 NC_000014.8:TRAV10:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4911 rs2204954 14:22299150 A 28675 NC_000014.8:TRAV11:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=927 rs4981385 14:22316107 A ENSESTG00000026506 ENSESTT00000066756 Transcript upstream_gene_variant - - - - - - DISTANCE=4424 rs4981385 14:22316107 A 28683 NC_000014.8:TRAV8-3:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4628 rs4981385 14:22316107 A ENSESTG00000026501 ENSESTT00000066729 Transcript downstream_gene_variant - - - - - - DISTANCE=800 rs4981385 14:22316107 A ENSESTG00000026506 ENSESTT00000066739 Transcript upstream_gene_variant - - - - - - DISTANCE=4404 rs4981385 14:22316107 A 28684 NC_000014.8:TRAV8-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=704 rs6572223 14:22507217 T 28663 NC_000014.8:TRAV20:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1692 rs8018954 14:22513720 T 28663 NC_000014.8:TRAV20:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4321 rs10130750 14:22523315 A 28662 NC_000014.8:TRAV21:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2000 rs12894654 14:22529160 T - - - intergenic_variant - - - - - - rs2204981 14:22540391 T 28661 NC_000014.8:TRAV22:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=920 rs2103420 14:22541677 T 28661 NC_000014.8:TRAV22:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2206 rs6572265 14:22575189 T ENSESTG00000026558 ENSESTT00000066849 Transcript downstream_gene_variant - - - - - - DISTANCE=860 rs6572265 14:22575189 T 28659 NC_000014.8:TRAV24:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1066 rs8004196 14:22653518 G 28650 NC_000014.8:TRAV32:u_t_1 Transcript splice_region_variant,intron_variant - - - - - - rs8004196 14:22653518 G 28649 NC_000014.8:TRAV33:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4534 rs4982572 14:22661580 T 28649 NC_000014.8:TRAV33:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2972 rs2204965 14:22664881 T - - - intergenic_variant - - - - - - rs8016737 14:22683723 T - - - intergenic_variant - - - - - - rs4982575 14:22684513 G - - - intergenic_variant - - - - - - rs988439 14:22697252 A 28646 NC_000014.8:TRAV36DV7:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2103 rs988439 14:22697252 A ENSESTG00000026572 ENSESTT00000066873 Transcript downstream_gene_variant - - - - - - DISTANCE=1956 rs7141643 14:22824066 T ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs7141643 14:22824066 T ENSESTG00000026601 ENSESTT00000066980 Transcript intron_variant - - - - - - rs7141643 14:22824066 T ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs7141643 14:22824066 T ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs8005446 14:22824583 A ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs8005446 14:22824583 A ENSESTG00000026601 ENSESTT00000066980 Transcript intron_variant - - - - - - rs8005446 14:22824583 A ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs8005446 14:22824583 A ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs2331661 14:22827416 T ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs2331661 14:22827416 T ENSESTG00000026601 ENSESTT00000066980 Transcript intron_variant - - - - - - rs2331661 14:22827416 T ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs2331661 14:22827416 T ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs2141987 14:22830317 T ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs2141987 14:22830317 T ENSESTG00000026601 ENSESTT00000066980 Transcript intron_variant - - - - - - rs2141987 14:22830317 T ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs2141987 14:22830317 T ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs8181911 14:22835559 A ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs8181911 14:22835559 A ENSESTG00000026601 ENSESTT00000066980 Transcript intron_variant - - - - - - rs8181911 14:22835559 A ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs8181911 14:22835559 A ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs6572413 14:22842924 T ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs6572413 14:22842924 T ENSESTG00000026601 ENSESTT00000066980 Transcript intron_variant - - - - - - rs6572413 14:22842924 T ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs6572413 14:22842924 T ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs4982621 14:22855097 A ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs4982621 14:22855097 A ENSESTG00000026609 ENSESTT00000067022 Transcript intron_variant - - - - - - rs4982621 14:22855097 A ENSESTG00000026601 ENSESTT00000066980 Transcript downstream_gene_variant - - - - - - DISTANCE=1625 rs4982621 14:22855097 A ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs4982621 14:22855097 A ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs4982621 14:22855097 A ENSESTG00000026609 ENSESTT00000067003 Transcript intron_variant - - - - - - rs1475958 14:22867593 T ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs1475958 14:22867593 T ENSESTG00000026609 ENSESTT00000067022 Transcript intron_variant - - - - - - rs1475958 14:22867593 T ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs1475958 14:22867593 T ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs1475958 14:22867593 T ENSESTG00000026609 ENSESTT00000067003 Transcript intron_variant - - - - - - rs9671986 14:22868838 T ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs9671986 14:22868838 T ENSESTG00000026609 ENSESTT00000067022 Transcript intron_variant - - - - - - rs9671986 14:22868838 T ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs9671986 14:22868838 T ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs9671986 14:22868838 T ENSESTG00000026609 ENSESTT00000067003 Transcript intron_variant - - - - - - rs6420850 14:22871576 A - ENSR00001455913 RegulatoryFeature regulatory_region_variant - - - - - - rs6420850 14:22871576 A ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs6420850 14:22871576 A ENSESTG00000026609 ENSESTT00000067022 Transcript intron_variant - - - - - - rs6420850 14:22871576 A ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs6420850 14:22871576 A ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs6420850 14:22871576 A ENSESTG00000026609 ENSESTT00000067003 Transcript intron_variant - - - - - - rs1040304 14:22872177 T ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs1040304 14:22872177 T ENSESTG00000026609 ENSESTT00000067022 Transcript intron_variant - - - - - - rs1040304 14:22872177 T ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs1040304 14:22872177 T ENSESTG00000026579 ENSESTT00000066904 Transcript intron_variant - - - - - - rs1040304 14:22872177 T ENSESTG00000026609 ENSESTT00000067003 Transcript intron_variant - - - - - - rs227868 14:22956149 T ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs227868 14:22956149 T ENSESTG00000022407 ENSESTT00000056610 Transcript intron_variant - - - - - - rs227868 14:22956149 T ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs227868 14:22956149 T 28705 NC_000014.8:TRAJ50:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1432 rs227868 14:22956149 T 28701 NC_000014.8:TRAJ54:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4814 rs227868 14:22956149 T 28707 NC_000014.8:TRAJ48:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3330 rs227868 14:22956149 T 28702 NC_000014.8:TRAJ53:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4091 rs227868 14:22956149 T 28703 NC_000014.8:TRAJ52:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=865 rs227868 14:22956149 T 28706 NC_000014.8:TRAJ49:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2327 rs227868 14:22956149 T ENSESTG00000026609 ENSESTT00000067003 Transcript upstream_gene_variant - - - - - - DISTANCE=4204 rs227025 14:22997879 C 28737 NC_000014.8:TRAJ18:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3194 rs227025 14:22997879 C ENSESTG00000026586 ENSESTT00000066957 Transcript intron_variant - - - - - - rs227025 14:22997879 C ENSESTG00000022407 ENSESTT00000056610 Transcript intron_variant - - - - - - rs227025 14:22997879 C ENSESTG00000026586 ENSESTT00000066928 Transcript intron_variant - - - - - - rs227025 14:22997879 C 28745 NC_000014.8:TRAJ10:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4566 rs227025 14:22997879 C 28735 NC_000014.8:TRAJ20:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4527 rs227025 14:22997879 C 28743 NC_000014.8:TRAJ12:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3010 rs227025 14:22997879 C 28740 NC_000014.8:TRAJ15:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=701 rs227025 14:22997879 C 28739 NC_000014.8:TRAJ16:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=333 rs227025 14:22997879 C 28742 NC_000014.8:TRAJ13:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2147 rs227025 14:22997879 C 28744 NC_000014.8:TRAJ11:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3573 rs227025 14:22997879 C ENSESTG00000022407 ENSESTT00000056631 Transcript intron_variant - - - - - - rs227025 14:22997879 C 28736 NC_000014.8:TRAJ19:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3587 rs227025 14:22997879 C 28738 NC_000014.8:TRAJ17:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2005 rs227025 14:22997879 C 28741 NC_000014.8:TRAJ14:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1399 rs4144360 14:23504238 A - ENSR00001455969 RegulatoryFeature regulatory_region_variant - - - - - - rs4144360 14:23504238 A ENSESTG00000023661 ENSESTT00000059743 Transcript intron_variant - - - - - - rs4144360 14:23504238 A CCDS9584.1 CCDS9584.1 Transcript upstream_gene_variant - - - - - - DISTANCE=148 rs4144360 14:23504238 A CCDS45084.1 CCDS45084.1 Transcript upstream_gene_variant - - - - - - DISTANCE=148 rs4144360 14:23504238 A 5693 NM_001130725.1 Transcript intron_variant - - - - - - rs4144360 14:23504238 A ENSESTG00000023661 ENSESTT00000059778 Transcript upstream_gene_variant - - - - - - DISTANCE=302 rs4144360 14:23504238 A ENSESTG00000023661 ENSESTT00000059768 Transcript upstream_gene_variant - - - - - - DISTANCE=139 rs4144360 14:23504238 A 5693 NM_002797.3 Transcript 5_prime_UTR_variant 117 - - - - - rs4144360 14:23504238 A CCDS45083.1 CCDS45083.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1466 rs4144360 14:23504238 A ENSESTG00000022925 ENSESTT00000057809 Transcript 3_prime_UTR_variant 724 - - - - - rs4144360 14:23504238 A 5693 NM_001144932.1 Transcript 5_prime_UTR_variant 117 - - - - - rs150840 14:24141138 C - - - intergenic_variant - - - - - - rs4644771 14:24397606 A ENSESTG00000001576 ENSESTT00000003729 Transcript intron_variant - - - - - - rs3021119 14:24567498 C ENSESTG00000001549 ENSESTT00000003678 Transcript upstream_gene_variant - - - - - - DISTANCE=3199 rs3021119 14:24567498 C ENSESTG00000005419 ENSESTT00000013870 Transcript 5_prime_UTR_variant 88 - - - - - rs3021119 14:24567498 C CCDS9609.1 CCDS9609.1 Transcript missense_variant 362 362 121 Q/P cAa/cCa - PolyPhen=benign;SIFT=tolerated rs3021119 14:24567498 C ENSESTG00000005419 ENSESTT00000013864 Transcript 5_prime_UTR_variant 88 - - - - - rs3021119 14:24567498 C ENSESTG00000005419 ENSESTT00000013764 Transcript 5_prime_UTR_variant 410 - - - - - rs3021119 14:24567498 C ENSESTG00000001549 ENSESTT00000003674 Transcript upstream_gene_variant - - - - - - DISTANCE=3192 rs3021119 14:24567498 C 5106 NM_004563.2 Transcript missense_variant 494 362 121 Q/P cAa/cCa - PolyPhen=benign;SIFT=tolerated rs3021119 14:24567498 C 5106 NM_001018073.1 Transcript missense_variant 494 362 121 Q/P cAa/cCa - PolyPhen=benign;SIFT=tolerated rs3021119 14:24567498 C ENSESTG00000005419 ENSESTT00000013784 Transcript downstream_gene_variant - - - - - - DISTANCE=61 rs3021119 14:24567498 C ENSESTG00000001549 ENSESTT00000003670 Transcript upstream_gene_variant - - - - - - DISTANCE=3192 rs3021119 14:24567498 C ENSESTG00000005419 ENSESTT00000013774 Transcript downstream_gene_variant - - - - - - DISTANCE=1322 rs3021119 14:24567498 C ENSESTG00000005419 ENSESTT00000013788 Transcript downstream_gene_variant - - - - - - DISTANCE=1299 rs3021119 14:24567498 C CCDS41928.1 CCDS41928.1 Transcript missense_variant 362 362 121 Q/P cAa/cCa - PolyPhen=benign;SIFT=tolerated rs7493513 14:24816439 G - - - intergenic_variant - - - - - - rs7160997 14:26006299 G - - - intergenic_variant - - - - - - rs1120457 14:26193037 G - - - intergenic_variant - - - - - - rs6574734 14:26416587 G - - - intergenic_variant - - - - - - rs2753584 14:26435182 G - - - intergenic_variant - - - - - - rs178172 14:27012253 G ENSESTG00000003952 ENSESTT00000010022 Transcript intron_variant - - - - - - rs178172 14:27012253 G ENSESTG00000003952 ENSESTT00000010009 Transcript intron_variant - - - - - - rs178172 14:27012253 G 4857 NM_006491.2 Transcript intron_variant - - - - - - rs178172 14:27012253 G ENSESTG00000003952 ENSESTT00000010018 Transcript intron_variant - - - - - - rs178172 14:27012253 G ENSESTG00000003952 ENSESTT00000010033 Transcript intron_variant - - - - - - rs178172 14:27012253 G ENSESTG00000003952 ENSESTT00000010014 Transcript intron_variant - - - - - - rs178172 14:27012253 G CCDS9635.1 CCDS9635.1 Transcript intron_variant - - - - - - rs178172 14:27012253 G CCDS32060.1 CCDS32060.1 Transcript intron_variant - - - - - - rs178172 14:27012253 G CCDS32061.1 CCDS32061.1 Transcript intron_variant - - - - - - rs178172 14:27012253 G 4857 NM_006489.2 Transcript intron_variant - - - - - - rs178172 14:27012253 G ENSESTG00000003952 ENSESTT00000010029 Transcript intron_variant - - - - - - rs178172 14:27012253 G ENSESTG00000003952 ENSESTT00000010026 Transcript intron_variant - - - - - - rs178172 14:27012253 G ENSESTG00000003952 ENSESTT00000010012 Transcript intron_variant - - - - - - rs178172 14:27012253 G 4857 NM_002515.2 Transcript intron_variant - - - - - - rs202980 14:27741243 A - - - intergenic_variant - - - - - - rs203609 14:27745698 C - - - intergenic_variant - - - - - - rs203608 14:27748100 G - - - intergenic_variant - - - - - - rs4272939 14:28107951 T 100505967 NR_039992.1 Transcript non_coding_exon_variant,nc_transcript_variant 2644 - - - - - rs4272939 14:28107951 T ENSESTG00000010645 ENSESTT00000026628 Transcript downstream_gene_variant - - - - - - DISTANCE=1755 rs8013689 14:28916607 T - - - intergenic_variant - - - - - - rs4391985 14:29673999 T - ENSR00000415796 RegulatoryFeature regulatory_region_variant - - - - - - rs4391985 14:29673999 T - - - intergenic_variant - - - - - - rs2333483 14:29708451 C - - - intergenic_variant - - - - - - rs4445800 14:29731570 T ENSESTG00000020416 ENSESTT00000051247 Transcript downstream_gene_variant - - - - - - DISTANCE=2459 rs4445800 14:29731570 T ENSESTG00000020416 ENSESTT00000051265 Transcript downstream_gene_variant - - - - - - DISTANCE=2480 rs4246972 14:29747816 C - ENSR00001456194 RegulatoryFeature regulatory_region_variant - - - - - - rs4246972 14:29747816 C ENSESTG00000020416 ENSESTT00000051247 Transcript intron_variant - - - - - - rs4246972 14:29747816 C ENSESTG00000020416 ENSESTT00000051265 Transcript intron_variant - - - - - - rs4246972 14:29747816 C ENSESTG00000020416 ENSESTT00000051200 Transcript intron_variant - - - - - - rs6576286 14:29771763 G ENSESTG00000020416 ENSESTT00000051247 Transcript intron_variant - - - - - - rs6576286 14:29771763 G ENSESTG00000020416 ENSESTT00000051265 Transcript intron_variant - - - - - - rs6576286 14:29771763 G ENSESTG00000020416 ENSESTT00000051200 Transcript intron_variant - - - - - - rs4542566 14:29915622 G - - - intergenic_variant - - - - - - rs7161629 14:29917050 G - - - intergenic_variant - - - - - - rs1953718 14:30128737 G ENSESTG00000034179 ENSESTT00000086465 Transcript intron_variant - - - - - - rs1953718 14:30128737 G ENSESTG00000034179 ENSESTT00000086470 Transcript intron_variant - - - - - - rs1953718 14:30128737 G CCDS9637.1 CCDS9637.1 Transcript intron_variant - - - - - - rs1953718 14:30128737 G ENSESTG00000034179 ENSESTT00000086484 Transcript upstream_gene_variant - - - - - - DISTANCE=3022 rs1953718 14:30128737 G 5587 NM_002742.2 Transcript intron_variant - - - - - - rs1953718 14:30128737 G ENSESTG00000034179 ENSESTT00000086480 Transcript intron_variant - - - - - - rs1953718 14:30128737 G ENSESTG00000034179 ENSESTT00000086477 Transcript intron_variant - - - - - - rs179077 14:30793524 A - - - intergenic_variant - - - - - - rs8021047 14:30886826 A - - - intergenic_variant - - - - - - rs1956969 14:30933053 T ENSESTG00000029464 ENSESTT00000074149 Transcript intron_variant - - - - - - rs4981071 14:30934065 G ENSESTG00000029464 ENSESTT00000074149 Transcript intron_variant - - - - - - rs369646 14:31075870 T CCDS9638.1 CCDS9638.1 Transcript intron_variant - - - - - - rs369646 14:31075870 T ENSESTG00000028471 ENSESTT00000071880 Transcript intron_variant - - - - - - rs369646 14:31075870 T ENSESTG00000028471 ENSESTT00000071915 Transcript intron_variant - - - - - - rs369646 14:31075870 T ENSESTG00000028471 ENSESTT00000071948 Transcript intron_variant - - - - - - rs369646 14:31075870 T 55632 NM_017769.3 Transcript intron_variant - - - - - - rs396171 14:31075874 T CCDS9638.1 CCDS9638.1 Transcript intron_variant - - - - - - rs396171 14:31075874 T ENSESTG00000028471 ENSESTT00000071880 Transcript intron_variant - - - - - - rs396171 14:31075874 T ENSESTG00000028471 ENSESTT00000071915 Transcript intron_variant - - - - - - rs396171 14:31075874 T ENSESTG00000028471 ENSESTT00000071948 Transcript intron_variant - - - - - - rs396171 14:31075874 T 55632 NM_017769.3 Transcript intron_variant - - - - - - rs1315794 14:31582380 G 25831 NM_015382.2 Transcript missense_variant 6569 6080 2027 L/P cTt/cCt - PolyPhen=benign;SIFT=tolerated rs1315794 14:31582380 G ENSESTG00000029188 ENSESTT00000073591 Transcript missense_variant 197 197 66 L/P cTt/cCt - rs1315794 14:31582380 G CCDS41939.1 CCDS41939.1 Transcript missense_variant 6080 6080 2027 L/P cTt/cCt - PolyPhen=benign;SIFT=tolerated rs1315794 14:31582380 G ENSESTG00000028928 ENSESTT00000073089 Transcript downstream_gene_variant - - - - - - DISTANCE=693 rs1315794 14:31582380 G ENSESTG00000028928 ENSESTT00000073017 Transcript downstream_gene_variant - - - - - - DISTANCE=693 rs1315794 14:31582380 G ENSESTG00000028928 ENSESTT00000073081 Transcript intron_variant - - - - - - rs1315794 14:31582380 G ENSESTG00000028928 ENSESTT00000072976 Transcript downstream_gene_variant - - - - - - DISTANCE=693 rs1315794 14:31582380 G ENSESTG00000028928 ENSESTT00000073025 Transcript downstream_gene_variant - - - - - - DISTANCE=693 rs1315794 14:31582380 G ENSESTG00000029188 ENSESTT00000073615 Transcript missense_variant 190 188 63 L/P cTt/cCt - rs1315794 14:31582380 G ENSESTG00000028928 ENSESTT00000072840 Transcript downstream_gene_variant - - - - - - DISTANCE=1111 rs4981089 14:31685078 G - - - intergenic_variant - - - - - - rs1316235 14:32522025 G - - - intergenic_variant - - - - - - rs7150403 14:32939575 C - ENSR00001456390 RegulatoryFeature regulatory_region_variant - - - - - - rs7150403 14:32939575 C ENSESTG00000017550 ENSESTT00000044176 Transcript intron_variant - - - - - - rs7150403 14:32939575 C ENSESTG00000008227 ENSESTT00000020784 Transcript intron_variant - - - - - - rs7150403 14:32939575 C CCDS9644.1 CCDS9644.1 Transcript intron_variant - - - - - - rs7150403 14:32939575 C ENSESTG00000017550 ENSESTT00000044164 Transcript intron_variant - - - - - - rs7150403 14:32939575 C 9472 NM_004274.4 Transcript intron_variant - - - - - - rs1998024 14:33377456 C - - - intergenic_variant - - - - - - rs4143872 14:33663187 C CCDS53891.1 CCDS53891.1 Transcript intron_variant - - - - - - rs4143872 14:33663187 C 64067 NM_001165893.1 Transcript intron_variant - - - - - - rs4143872 14:33663187 C CCDS55912.1 CCDS55912.1 Transcript intron_variant - - - - - - rs4143872 14:33663187 C CCDS53892.1 CCDS53892.1 Transcript intron_variant - - - - - - rs4143872 14:33663187 C 64067 NM_001164749.1 Transcript intron_variant - - - - - - rs4143872 14:33663187 C 64067 NM_022123.2 Transcript intron_variant - - - - - - rs4143872 14:33663187 C 64067 NM_173159.2 Transcript intron_variant - - - - - - rs4143872 14:33663187 C CCDS9645.1 CCDS9645.1 Transcript intron_variant - - - - - - rs4143872 14:33663187 C ENSESTG00000017536 ENSESTT00000044123 Transcript intron_variant - - - - - - rs243304 14:33738052 C CCDS53891.1 CCDS53891.1 Transcript intron_variant - - - - - - rs243304 14:33738052 C 64067 NM_001165893.1 Transcript intron_variant - - - - - - rs243304 14:33738052 C CCDS55912.1 CCDS55912.1 Transcript intron_variant - - - - - - rs243304 14:33738052 C CCDS53892.1 CCDS53892.1 Transcript intron_variant - - - - - - rs243304 14:33738052 C 64067 NM_001164749.1 Transcript intron_variant - - - - - - rs243304 14:33738052 C 64067 NM_022123.2 Transcript intron_variant - - - - - - rs243304 14:33738052 C 64067 NM_173159.2 Transcript intron_variant - - - - - - rs243304 14:33738052 C CCDS9645.1 CCDS9645.1 Transcript intron_variant - - - - - - rs243304 14:33738052 C ENSESTG00000017536 ENSESTT00000044123 Transcript intron_variant - - - - - - rs1315136 14:33827336 G CCDS53891.1 CCDS53891.1 Transcript intron_variant - - - - - - rs1315136 14:33827336 G 64067 NM_001165893.1 Transcript intron_variant - - - - - - rs1315136 14:33827336 G CCDS55912.1 CCDS55912.1 Transcript intron_variant - - - - - - rs1315136 14:33827336 G CCDS53892.1 CCDS53892.1 Transcript intron_variant - - - - - - rs1315136 14:33827336 G 64067 NM_001164749.1 Transcript intron_variant - - - - - - rs1315136 14:33827336 G 64067 NM_022123.2 Transcript intron_variant - - - - - - rs1315136 14:33827336 G 64067 NM_173159.2 Transcript intron_variant - - - - - - rs1315136 14:33827336 G CCDS9645.1 CCDS9645.1 Transcript intron_variant - - - - - - rs1315136 14:33827336 G ENSESTG00000017536 ENSESTT00000044123 Transcript intron_variant - - - - - - rs1315127 14:33837498 T CCDS53891.1 CCDS53891.1 Transcript intron_variant - - - - - - rs1315127 14:33837498 T 64067 NM_001165893.1 Transcript intron_variant - - - - - - rs1315127 14:33837498 T CCDS55912.1 CCDS55912.1 Transcript intron_variant - - - - - - rs1315127 14:33837498 T CCDS53892.1 CCDS53892.1 Transcript intron_variant - - - - - - rs1315127 14:33837498 T 64067 NM_001164749.1 Transcript intron_variant - - - - - - rs1315127 14:33837498 T ENSESTG00000030848 ENSESTT00000077699 Transcript intron_variant - - - - - - rs1315127 14:33837498 T 64067 NM_022123.2 Transcript intron_variant - - - - - - rs1315127 14:33837498 T 64067 NM_173159.2 Transcript intron_variant - - - - - - rs1315127 14:33837498 T ENSESTG00000030848 ENSESTT00000077718 Transcript intron_variant - - - - - - rs1315127 14:33837498 T CCDS9645.1 CCDS9645.1 Transcript intron_variant - - - - - - rs1315127 14:33837498 T ENSESTG00000017536 ENSESTT00000044123 Transcript intron_variant - - - - - - rs7146494 14:34185325 T CCDS53891.1 CCDS53891.1 Transcript intron_variant - - - - - - rs7146494 14:34185325 T 64067 NM_001165893.1 Transcript intron_variant - - - - - - rs7146494 14:34185325 T CCDS55912.1 CCDS55912.1 Transcript intron_variant - - - - - - rs7146494 14:34185325 T CCDS53892.1 CCDS53892.1 Transcript intron_variant - - - - - - rs7146494 14:34185325 T 64067 NM_001164749.1 Transcript intron_variant - - - - - - rs7146494 14:34185325 T 64067 NM_022123.2 Transcript intron_variant - - - - - - rs7146494 14:34185325 T 64067 NM_173159.2 Transcript intron_variant - - - - - - rs7146494 14:34185325 T ENSESTG00000030848 ENSESTT00000077718 Transcript intron_variant - - - - - - rs7146494 14:34185325 T CCDS9645.1 CCDS9645.1 Transcript intron_variant - - - - - - rs3121069 14:34443566 T ENSESTG00000030887 ENSESTT00000077829 Transcript intron_variant - - - - - - rs3102135 14:34515308 A ENSESTG00000030887 ENSESTT00000077829 Transcript intron_variant - - - - - - rs797357 14:34564952 C ENSESTG00000030887 ENSESTT00000077806 Transcript intron_variant - - - - - - rs797357 14:34564952 C ENSESTG00000030876 ENSESTT00000077756 Transcript intron_variant - - - - - - rs797357 14:34564952 C ENSESTG00000030887 ENSESTT00000077790 Transcript downstream_gene_variant - - - - - - DISTANCE=417 rs797357 14:34564952 C ENSESTG00000030887 ENSESTT00000077829 Transcript intron_variant - - - - - - rs2149905 14:34690397 A - ENSR00000416278 RegulatoryFeature regulatory_region_variant - - - - - - rs2149905 14:34690397 A ENSESTG00000030887 ENSESTT00000077806 Transcript intron_variant - - - - - - rs2149905 14:34690397 A ENSESTG00000030887 ENSESTT00000077790 Transcript intron_variant - - - - - - rs2149905 14:34690397 A ENSESTG00000030887 ENSESTT00000077829 Transcript intron_variant - - - - - - rs6571644 14:34741620 T - - - intergenic_variant - - - - - - rs11156835 14:34778871 C - - - intergenic_variant - - - - - - rs799662 14:35389555 T ENSESTG00000025647 ENSESTT00000064716 Transcript downstream_gene_variant - - - - - - DISTANCE=533 rs10130519 14:35598085 T ENSESTG00000025383 ENSESTT00000064138 Transcript intron_variant - - - - - - rs10130519 14:35598085 T CCDS58312.1 CCDS58312.1 Transcript intron_variant - - - - - - rs10130519 14:35598085 T CCDS32063.1 CCDS32063.1 Transcript intron_variant - - - - - - rs10130519 14:35598085 T 9692 NM_001256680.1 Transcript intron_variant - - - - - - rs10130519 14:35598085 T 9692 NM_001256679.1 Transcript intron_variant - - - - - - rs10130519 14:35598085 T 9692 NM_014672.3 Transcript intron_variant - - - - - - rs10130519 14:35598085 T 9692 NM_001256681.1 Transcript intron_variant - - - - - - rs10130519 14:35598085 T CCDS58314.1 CCDS58314.1 Transcript intron_variant - - - - - - rs10130519 14:35598085 T 9692 NM_001256678.1 Transcript intron_variant - - - - - - rs10130519 14:35598085 T CCDS58313.1 CCDS58313.1 Transcript intron_variant - - - - - - rs911502 14:36545836 C - - - intergenic_variant - - - - - - rs7141200 14:36876152 G - - - intergenic_variant - - - - - - rs848077 14:37288105 G 89874 NM_030631.3 Transcript intron_variant - - - - - - rs848077 14:37288105 G CCDS55913.1 CCDS55913.1 Transcript intron_variant - - - - - - rs848077 14:37288105 G CCDS9663.1 CCDS9663.1 Transcript intron_variant - - - - - - rs848077 14:37288105 G 89874 NM_001171170.1 Transcript intron_variant - - - - - - rs848074 14:37290412 G 89874 NM_030631.3 Transcript intron_variant - - - - - - rs848074 14:37290412 G CCDS55913.1 CCDS55913.1 Transcript intron_variant - - - - - - rs848074 14:37290412 G CCDS9663.1 CCDS9663.1 Transcript intron_variant - - - - - - rs848074 14:37290412 G 89874 NM_001171170.1 Transcript intron_variant - - - - - - rs4409994 14:37649073 A - - - intergenic_variant - - - - - - rs11623620 14:37788106 T 145282 NM_001195296.1 Transcript intron_variant - - - - - - rs11623620 14:37788106 T 145282 NM_001195297.1 Transcript intron_variant - - - - - - rs11623620 14:37788106 T 145282 NM_138731.6 Transcript intron_variant - - - - - - rs11623620 14:37788106 T ENSESTG00000033957 ENSESTT00000085809 Transcript intron_variant - - - - - - rs11623620 14:37788106 T ENSESTG00000012388 ENSESTT00000031077 Transcript intron_variant - - - - - - rs11623620 14:37788106 T ENSESTG00000033957 ENSESTT00000085813 Transcript intron_variant - - - - - - rs11623620 14:37788106 T CCDS9664.1 CCDS9664.1 Transcript intron_variant - - - - - - rs1950822 14:37966576 C 145282 NM_001195296.1 Transcript intron_variant - - - - - - rs1950822 14:37966576 C 145282 NM_001195297.1 Transcript intron_variant - - - - - - rs1950822 14:37966576 C 145282 NM_138731.6 Transcript intron_variant - - - - - - rs1950822 14:37966576 C ENSESTG00000033957 ENSESTT00000085809 Transcript intron_variant - - - - - - rs1950822 14:37966576 C ENSESTG00000012388 ENSESTT00000031077 Transcript intron_variant - - - - - - rs1950822 14:37966576 C CCDS9664.1 CCDS9664.1 Transcript intron_variant - - - - - - rs1950817 14:38048834 A ENSESTG00000033983 ENSESTT00000085904 Transcript downstream_gene_variant - - - - - - DISTANCE=644 rs1957591 14:38153364 A 319089 XM_003846351.1 Transcript intron_variant - - - - - - rs8014429 14:38242401 T - - - intergenic_variant - - - - - - rs4901251 14:38246748 C - - - intergenic_variant - - - - - - rs1952793 14:38324777 A - - - intergenic_variant - - - - - - rs8010795 14:38354441 A - - - intergenic_variant - - - - - - rs2812077 14:38651270 C - - - intergenic_variant - - - - - - rs4442713 14:38685055 T 6751 NM_001049.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2787 rs4287474 14:38918842 A - - - intergenic_variant - - - - - - rs7140612 14:38945990 T - - - intergenic_variant - - - - - - rs12878980 14:38951604 C - ENSR00001024070 RegulatoryFeature regulatory_region_variant - - - - - - rs12878980 14:38951604 C - - - intergenic_variant - - - - - - rs4318118 14:38998433 A - - - intergenic_variant - - - - - - rs6571873 14:39289444 C ENSESTG00000026885 ENSESTT00000067764 Transcript intron_variant - - - - - - rs6571873 14:39289444 C 283547 NR_039982.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6571873 14:39289444 C ENSESTG00000026885 ENSESTT00000067751 Transcript intron_variant - - - - - - rs2415520 14:39353507 G 283547 NR_039982.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2415520 14:39353507 G ENSESTG00000026394 ENSESTT00000066504 Transcript intron_variant - - - - - - rs2164067 14:39702914 A - ENSR00000416874 RegulatoryFeature regulatory_region_variant - - - - - - rs2164067 14:39702914 A 117153 NM_054024.3 Transcript upstream_gene_variant - - - - - - DISTANCE=211 rs2164067 14:39702914 A ENSESTG00000026632 ENSESTT00000067104 Transcript upstream_gene_variant - - - - - - DISTANCE=206 rs2164067 14:39702914 A ENSESTG00000026632 ENSESTT00000067126 Transcript upstream_gene_variant - - - - - - DISTANCE=211 rs2164067 14:39702914 A ENSESTG00000026632 ENSESTT00000067090 Transcript intron_variant - - - - - - rs2164067 14:39702914 A CCDS9672.1 CCDS9672.1 Transcript upstream_gene_variant - - - - - - DISTANCE=405 rs1950632 14:40079526 A - - - intergenic_variant - - - - - - rs10150561 14:40288005 T - - - intergenic_variant - - - - - - rs11157093 14:40502306 C - - - intergenic_variant - - - - - - rs10131033 14:41090460 T - - - intergenic_variant - - - - - - rs10137000 14:41134870 T - - - intergenic_variant - - - - - - rs4903969 14:41137755 T - - - intergenic_variant - - - - - - rs1176855 14:41193977 T - - - intergenic_variant - - - - - - rs2600590 14:41455555 T - - - intergenic_variant - - - - - - rs2799814 14:41479247 A - - - intergenic_variant - - - - - - rs1782165 14:41772214 A - - - intergenic_variant - - - - - - rs4362303 14:42094676 C ENSESTG00000031700 ENSESTT00000079987 Transcript intron_variant - - - - - - rs4362303 14:42094676 C ENSESTG00000031700 ENSESTT00000080001 Transcript intron_variant - - - - - - rs4362303 14:42094676 C 145581 NM_152447.3 Transcript intron_variant - - - - - - rs10148466 14:42998026 C - - - intergenic_variant - - - - - - rs7156634 14:43611181 C - - - intergenic_variant - - - - - - rs2805842 14:43849202 T - - - intergenic_variant - - - - - - rs6572198 14:43931812 A - - - intergenic_variant - - - - - - rs6572225 14:44381375 T - - - intergenic_variant - - - - - - rs1957492 14:44453555 C - - - intergenic_variant - - - - - - rs1955993 14:44563220 T - - - intergenic_variant - - - - - - rs1959208 14:44814967 T - - - intergenic_variant - - - - - - rs811076 14:45240000 T ENSESTG00000006494 ENSESTT00000016341 Transcript intron_variant - - - - - - rs2144110 14:45361680 A 122525 NM_001017923.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4827 rs2144110 14:45361680 A ENSESTG00000012904 ENSESTT00000032363 Transcript upstream_gene_variant - - - - - - DISTANCE=4818 rs2144110 14:45361680 A ENSESTG00000006490 ENSESTT00000016333 Transcript intron_variant - - - - - - rs8020185 14:45374038 G CCDS32069.1 CCDS32069.1 Transcript intron_variant - - - - - - rs8020185 14:45374038 G 122525 NM_001017923.1 Transcript intron_variant - - - - - - rs8020185 14:45374038 G ENSESTG00000012904 ENSESTT00000032363 Transcript intron_variant - - - - - - rs8020185 14:45374038 G ENSESTG00000006482 ENSESTT00000016327 Transcript intron_variant - - - - - - rs8020185 14:45374038 G ENSESTG00000012904 ENSESTT00000032367 Transcript intron_variant - - - - - - rs170542 14:45610117 C ENSESTG00000006389 ENSESTT00000016123 Transcript downstream_gene_variant - - - - - - DISTANCE=3246 rs170542 14:45610117 C CCDS32070.1 CCDS32070.1 Transcript intron_variant - - - - - - rs170542 14:45610117 C 57697 NM_020937.2 Transcript intron_variant - - - - - - rs4906578 14:45900572 G - - - intergenic_variant - - - - - - rs10444709 14:45917237 T - - - intergenic_variant - - - - - - rs4906581 14:46049750 C - - - intergenic_variant - - - - - - rs8007492 14:46070860 C - - - intergenic_variant - - - - - - rs1266269 14:46179185 C ENSESTG00000008612 ENSESTT00000021647 Transcript intron_variant - - - - - - rs1266269 14:46179185 C ENSESTG00000008612 ENSESTT00000021660 Transcript upstream_gene_variant - - - - - - DISTANCE=2078 rs1266269 14:46179185 C ENSESTG00000008612 ENSESTT00000021651 Transcript intron_variant - - - - - - rs1266269 14:46179185 C ENSESTG00000008612 ENSESTT00000021656 Transcript intron_variant - - - - - - rs1266234 14:46209461 G - - - intergenic_variant - - - - - - rs1770942 14:46241979 G - - - intergenic_variant - - - - - - rs1770955 14:46254151 T - - - intergenic_variant - - - - - - rs396311 14:46318118 C - - - intergenic_variant - - - - - - rs425522 14:46320998 T - - - intergenic_variant - - - - - - rs8006547 14:46454646 T - - - intergenic_variant - - - - - - rs3118976 14:46533606 C - - - intergenic_variant - - - - - - rs3118978 14:46534139 C - - - intergenic_variant - - - - - - rs858880 14:46714920 C - - - intergenic_variant - - - - - - rs1953921 14:46775935 A - - - intergenic_variant - - - - - - rs7140676 14:46830701 T - - - intergenic_variant - - - - - - rs1669800 14:46920589 T - - - intergenic_variant - - - - - - rs2642085 14:46996128 C ENSESTG00000016727 ENSESTT00000041980 Transcript intron_variant - - - - - - rs2199460 14:47125004 A CCDS32071.1 CCDS32071.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4065 rs2199460 14:47125004 A ENSESTG00000016727 ENSESTT00000041987 Transcript upstream_gene_variant - - - - - - DISTANCE=4356 rs2199460 14:47125004 A ENSESTG00000016727 ENSESTT00000041980 Transcript upstream_gene_variant - - - - - - DISTANCE=4293 rs2199460 14:47125004 A ENSESTG00000016727 ENSESTT00000041973 Transcript upstream_gene_variant - - - - - - DISTANCE=4152 rs2199460 14:47125004 A ENSESTG00000016727 ENSESTT00000041992 Transcript upstream_gene_variant - - - - - - DISTANCE=4363 rs2199460 14:47125004 A 140801 NM_080746.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3976 rs2199460 14:47125004 A ENSESTG00000016727 ENSESTT00000041959 Transcript upstream_gene_variant - - - - - - DISTANCE=4092 rs2126467 14:47146038 A - - - intergenic_variant - - - - - - rs1462388 14:47225739 T - - - intergenic_variant - - - - - - rs2933219 14:47243442 T - - - intergenic_variant - - - - - - rs3007096 14:47244366 G - - - intergenic_variant - - - - - - rs4476092 14:47246151 T - - - intergenic_variant - - - - - - rs2933217 14:47249326 G - - - intergenic_variant - - - - - - rs2933193 14:47296132 A - - - intergenic_variant - - - - - - rs3007130 14:47317046 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs3007130 14:47317046 T ENSESTG00000016693 ENSESTT00000041938 Transcript intron_variant - - - - - - rs3007130 14:47317046 T ENSESTG00000016693 ENSESTT00000041928 Transcript intron_variant - - - - - - rs3007130 14:47317046 T ENSESTG00000016693 ENSESTT00000041930 Transcript intron_variant - - - - - - rs3007130 14:47317046 T CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs3007130 14:47317046 T 161357 NM_182830.3 Transcript intron_variant - - - - - - rs3007130 14:47317046 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs3007130 14:47317046 T ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs2933210 14:47317960 A CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2933210 14:47317960 A ENSESTG00000016693 ENSESTT00000041938 Transcript intron_variant - - - - - - rs2933210 14:47317960 A ENSESTG00000016693 ENSESTT00000041928 Transcript intron_variant - - - - - - rs2933210 14:47317960 A ENSESTG00000016693 ENSESTT00000041930 Transcript intron_variant - - - - - - rs2933210 14:47317960 A CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs2933210 14:47317960 A 161357 NM_182830.3 Transcript intron_variant - - - - - - rs2933210 14:47317960 A 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2933210 14:47317960 A ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs2933214 14:47323227 C CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2933214 14:47323227 C ENSESTG00000016693 ENSESTT00000041938 Transcript intron_variant - - - - - - rs2933214 14:47323227 C ENSESTG00000016693 ENSESTT00000041903 Transcript downstream_gene_variant - - - - - - DISTANCE=996 rs2933214 14:47323227 C ENSESTG00000016693 ENSESTT00000041928 Transcript intron_variant - - - - - - rs2933214 14:47323227 C CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs2933214 14:47323227 C ENSESTG00000016693 ENSESTT00000041930 Transcript intron_variant - - - - - - rs2933214 14:47323227 C 161357 NM_182830.3 Transcript intron_variant - - - - - - rs2933214 14:47323227 C 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2933214 14:47323227 C ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs2933212 14:47332383 A CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2933212 14:47332383 A ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs2933212 14:47332383 A ENSESTG00000016693 ENSESTT00000041928 Transcript intron_variant - - - - - - rs2933212 14:47332383 A ENSESTG00000016693 ENSESTT00000041930 Transcript intron_variant - - - - - - rs2933212 14:47332383 A CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs2933212 14:47332383 A 161357 NM_182830.3 Transcript intron_variant - - - - - - rs2933212 14:47332383 A 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2933212 14:47332383 A ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs2933207 14:47338796 G CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2933207 14:47338796 G ENSESTG00000016693 ENSESTT00000041848 Transcript downstream_gene_variant - - - - - - DISTANCE=4329 rs2933207 14:47338796 G ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs2933207 14:47338796 G ENSESTG00000016693 ENSESTT00000041928 Transcript intron_variant - - - - - - rs2933207 14:47338796 G CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs2933207 14:47338796 G ENSESTG00000016693 ENSESTT00000041930 Transcript intron_variant - - - - - - rs2933207 14:47338796 G ENSESTG00000016693 ENSESTT00000041908 Transcript downstream_gene_variant - - - - - - DISTANCE=4448 rs2933207 14:47338796 G 161357 NM_182830.3 Transcript intron_variant - - - - - - rs2933207 14:47338796 G 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2933207 14:47338796 G ENSESTG00000016693 ENSESTT00000041923 Transcript downstream_gene_variant - - - - - - DISTANCE=3810 rs2933207 14:47338796 G ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs3007094 14:47340138 A CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs3007094 14:47340138 A ENSESTG00000016693 ENSESTT00000041848 Transcript downstream_gene_variant - - - - - - DISTANCE=2987 rs3007094 14:47340138 A ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs3007094 14:47340138 A ENSESTG00000016693 ENSESTT00000041928 Transcript intron_variant - - - - - - rs3007094 14:47340138 A CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs3007094 14:47340138 A ENSESTG00000016693 ENSESTT00000041930 Transcript intron_variant - - - - - - rs3007094 14:47340138 A ENSESTG00000016693 ENSESTT00000041908 Transcript downstream_gene_variant - - - - - - DISTANCE=3106 rs3007094 14:47340138 A 161357 NM_182830.3 Transcript intron_variant - - - - - - rs3007094 14:47340138 A 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs3007094 14:47340138 A ENSESTG00000016693 ENSESTT00000041923 Transcript downstream_gene_variant - - - - - - DISTANCE=2468 rs3007094 14:47340138 A ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs2933209 14:47341652 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2933209 14:47341652 T ENSESTG00000016693 ENSESTT00000041848 Transcript downstream_gene_variant - - - - - - DISTANCE=1473 rs2933209 14:47341652 T ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs2933209 14:47341652 T ENSESTG00000016693 ENSESTT00000041928 Transcript intron_variant - - - - - - rs2933209 14:47341652 T CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs2933209 14:47341652 T ENSESTG00000016693 ENSESTT00000041930 Transcript intron_variant - - - - - - rs2933209 14:47341652 T ENSESTG00000016693 ENSESTT00000041908 Transcript downstream_gene_variant - - - - - - DISTANCE=1592 rs2933209 14:47341652 T 161357 NM_182830.3 Transcript intron_variant - - - - - - rs2933209 14:47341652 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2933209 14:47341652 T ENSESTG00000016693 ENSESTT00000041923 Transcript downstream_gene_variant - - - - - - DISTANCE=954 rs2933209 14:47341652 T ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs3007095 14:47343536 A CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs3007095 14:47343536 A ENSESTG00000016693 ENSESTT00000041848 Transcript intron_variant - - - - - - rs3007095 14:47343536 A ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs3007095 14:47343536 A ENSESTG00000016693 ENSESTT00000041928 Transcript intron_variant - - - - - - rs3007095 14:47343536 A CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs3007095 14:47343536 A ENSESTG00000016693 ENSESTT00000041930 Transcript intron_variant - - - - - - rs3007095 14:47343536 A ENSESTG00000016693 ENSESTT00000041908 Transcript intron_variant - - - - - - rs3007095 14:47343536 A 161357 NM_182830.3 Transcript intron_variant - - - - - - rs3007095 14:47343536 A 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs3007095 14:47343536 A ENSESTG00000016693 ENSESTT00000041923 Transcript intron_variant - - - - - - rs3007095 14:47343536 A ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs3007099 14:47362597 T ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs3007099 14:47362597 T CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs3007099 14:47362597 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs3007099 14:47362597 T 161357 NM_182830.3 Transcript intron_variant - - - - - - rs3007099 14:47362597 T ENSESTG00000016693 ENSESTT00000041848 Transcript intron_variant - - - - - - rs3007099 14:47362597 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs3007099 14:47362597 T ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs3007109 14:47371261 G ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs3007109 14:47371261 G CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs3007109 14:47371261 G CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs3007109 14:47371261 G 161357 NM_182830.3 Transcript intron_variant - - - - - - rs3007109 14:47371261 G ENSESTG00000016693 ENSESTT00000041848 Transcript intron_variant - - - - - - rs3007109 14:47371261 G 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs3007109 14:47371261 G ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs10137187 14:47373175 C ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs10137187 14:47373175 C CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs10137187 14:47373175 C CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs10137187 14:47373175 C 161357 NM_182830.3 Transcript intron_variant - - - - - - rs10137187 14:47373175 C ENSESTG00000016693 ENSESTT00000041848 Transcript intron_variant - - - - - - rs10137187 14:47373175 C 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs10137187 14:47373175 C ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs2933186 14:47377239 A ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs2933186 14:47377239 A CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs2933186 14:47377239 A CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2933186 14:47377239 A 161357 NM_182830.3 Transcript intron_variant - - - - - - rs2933186 14:47377239 A ENSESTG00000016693 ENSESTT00000041848 Transcript intron_variant - - - - - - rs2933186 14:47377239 A 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2933186 14:47377239 A ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs3007114 14:47377314 T ENSESTG00000016693 ENSESTT00000041903 Transcript intron_variant - - - - - - rs3007114 14:47377314 T CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs3007114 14:47377314 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs3007114 14:47377314 T 161357 NM_182830.3 Transcript intron_variant - - - - - - rs3007114 14:47377314 T ENSESTG00000016693 ENSESTT00000041848 Transcript intron_variant - - - - - - rs3007114 14:47377314 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs3007114 14:47377314 T ENSESTG00000016693 ENSESTT00000041894 Transcript intron_variant - - - - - - rs12897120 14:47469688 T ENSESTG00000016635 ENSESTT00000041737 Transcript intron_variant - - - - - - rs12897120 14:47469688 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs12897120 14:47469688 T ENSESTG00000016635 ENSESTT00000041744 Transcript intron_variant - - - - - - rs12897120 14:47469688 T ENSESTG00000016635 ENSESTT00000041811 Transcript intron_variant - - - - - - rs12897120 14:47469688 T CCDS41948.1 CCDS41948.1 Transcript intron_variant - - - - - - rs12897120 14:47469688 T 161357 NM_182830.3 Transcript intron_variant - - - - - - rs12897120 14:47469688 T ENSESTG00000016635 ENSESTT00000041809 Transcript intron_variant - - - - - - rs12897120 14:47469688 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs9671885 14:47756241 T ENSESTG00000016635 ENSESTT00000041737 Transcript intron_variant - - - - - - rs9671885 14:47756241 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs9671885 14:47756241 T ENSESTG00000016635 ENSESTT00000041744 Transcript intron_variant - - - - - - rs9671885 14:47756241 T ENSESTG00000016635 ENSESTT00000041818 Transcript intron_variant - - - - - - rs9671885 14:47756241 T ENSESTG00000016635 ENSESTT00000041811 Transcript intron_variant - - - - - - rs9671885 14:47756241 T 161357 NM_182830.3 Transcript intron_variant - - - - - - rs9671885 14:47756241 T ENSESTG00000016635 ENSESTT00000041809 Transcript intron_variant - - - - - - rs9671885 14:47756241 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs9671885 14:47756241 T ENSESTG00000016635 ENSESTT00000041774 Transcript intron_variant - - - - - - rs9671885 14:47756241 T ENSESTG00000016635 ENSESTT00000041790 Transcript intron_variant - - - - - - rs4609741 14:47795000 G ENSESTG00000016635 ENSESTT00000041737 Transcript intron_variant - - - - - - rs4609741 14:47795000 G CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs4609741 14:47795000 G 161357 NM_182830.3 Transcript intron_variant - - - - - - rs4609741 14:47795000 G ENSESTG00000016635 ENSESTT00000041744 Transcript intron_variant - - - - - - rs4609741 14:47795000 G ENSESTG00000016635 ENSESTT00000041790 Transcript intron_variant - - - - - - rs4609741 14:47795000 G ENSESTG00000016635 ENSESTT00000041774 Transcript intron_variant - - - - - - rs4609741 14:47795000 G 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2416053 14:47822226 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2416053 14:47822226 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs4492965 14:47853638 A CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs4492965 14:47853638 A 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs8020717 14:47863528 C CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs8020717 14:47863528 C 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs8017117 14:47890533 C CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs8017117 14:47890533 C 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2416072 14:47897578 C CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2416072 14:47897578 C 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs6572424 14:47900158 A CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs6572424 14:47900158 A 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs4900761 14:47905852 G CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs4900761 14:47905852 G 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs10132906 14:47910935 T ENSESTG00000004955 ENSESTT00000012582 Transcript downstream_gene_variant - - - - - - DISTANCE=2504 rs10132906 14:47910935 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs10132906 14:47910935 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2000027 14:47911808 A - ENSR00001456941 RegulatoryFeature regulatory_region_variant - - - - - - rs2000027 14:47911808 A ENSESTG00000004955 ENSESTT00000012582 Transcript downstream_gene_variant - - - - - - DISTANCE=1631 rs2000027 14:47911808 A CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2000027 14:47911808 A 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs1890800 14:47913775 T ENSESTG00000004955 ENSESTT00000012582 Transcript intron_variant - - - - - - rs1890800 14:47913775 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs1890800 14:47913775 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs4900762 14:47915970 G ENSESTG00000004955 ENSESTT00000012582 Transcript intron_variant - - - - - - rs4900762 14:47915970 G CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs4900762 14:47915970 G 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs1884223 14:48052276 C CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs1884223 14:48052276 C 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs10131310 14:48061407 A CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs10131310 14:48061407 A 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs1164631 14:48097747 C CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs1164631 14:48097747 C 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2416098 14:48124210 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs2416098 14:48124210 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs1956341 14:48132156 T CCDS45098.2 CCDS45098.2 Transcript intron_variant - - - - - - rs1956341 14:48132156 T 161357 NM_001113498.2 Transcript intron_variant - - - - - - rs2416109 14:48191684 T - - - intergenic_variant - - - - - - rs10143383 14:48202892 A - - - intergenic_variant - - - - - - rs4900798 14:48227496 C 100500919 NR_037503.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2702 rs1950758 14:48311300 T - - - intergenic_variant - - - - - - rs10151070 14:48365261 G - - - intergenic_variant - - - - - - rs698339 14:48541529 G - - - intergenic_variant - - - - - - rs12882177 14:48607158 G - - - intergenic_variant - - - - - - rs6420853 14:48860833 A - - - intergenic_variant - - - - - - rs2790541 14:49150227 T - - - intergenic_variant - - - - - - rs7148575 14:49398505 G - - - intergenic_variant - - - - - - rs4900909 14:49802569 A - - - intergenic_variant - - - - - - rs4900938 14:50036134 A - - - intergenic_variant - - - - - - rs4900978 14:50477643 C - ENSR00001457006 RegulatoryFeature regulatory_region_variant - - - - - - rs4900978 14:50477643 C 283551 NM_001012706.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3405 rs4900978 14:50477643 C ENSESTG00000031906 ENSESTT00000080523 Transcript intron_variant - - - - - - rs2934692 14:51097536 A 51062 NM_015915.4 Transcript intron_variant - - - - - - rs2934692 14:51097536 A ENSESTG00000001411 ENSESTT00000003372 Transcript intron_variant - - - - - - rs2934692 14:51097536 A CCDS9700.1 CCDS9700.1 Transcript intron_variant - - - - - - rs2934692 14:51097536 A 51062 NM_001127713.1 Transcript intron_variant - - - - - - rs2934692 14:51097536 A CCDS32077.1 CCDS32077.1 Transcript intron_variant - - - - - - rs2934692 14:51097536 A 51062 NM_181598.3 Transcript intron_variant - - - - - - rs2934692 14:51097536 A ENSESTG00000001571 ENSESTT00000003732 Transcript downstream_gene_variant - - - - - - DISTANCE=4256 rs2934692 14:51097536 A ENSESTG00000001571 ENSESTT00000003735 Transcript downstream_gene_variant - - - - - - DISTANCE=4313 rs2934692 14:51097536 A 60485 NM_021818.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2762 rs2934692 14:51097536 A CCDS9701.1 CCDS9701.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4365 rs11623955 14:51478270 T 114088 NM_015163.5 Transcript intron_variant - - - - - - rs11623955 14:51478270 T ENSESTG00000001458 ENSESTT00000003445 Transcript intron_variant - - - - - - rs11623955 14:51478270 T CCDS45105.1 CCDS45105.1 Transcript intron_variant - - - - - - rs11623955 14:51478270 T 114088 NM_052978.4 Transcript intron_variant - - - - - - rs11623955 14:51478270 T CCDS9703.1 CCDS9703.1 Transcript intron_variant - - - - - - rs3007166 14:51616001 A - - - intergenic_variant - - - - - - rs6572745 14:51809877 T ENSESTG00000011759 ENSESTT00000029514 Transcript downstream_gene_variant - - - - - - DISTANCE=192 rs6572745 14:51809877 T 283553 NR_038358.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4901117 14:51855622 G ENSESTG00000011903 ENSESTT00000029797 Transcript upstream_gene_variant - - - - - - DISTANCE=3297 rs10148800 14:51898815 A - - - intergenic_variant - - - - - - rs4435150 14:52259099 A - - - intergenic_variant - - - - - - rs1253695 14:52395206 C 54331 NM_001243774.1 Transcript intron_variant - - - - - - rs1253695 14:52395206 C ENSESTG00000011813 ENSESTT00000029623 Transcript intron_variant - - - - - - rs1253695 14:52395206 C ENSESTG00000011813 ENSESTT00000029644 Transcript intron_variant - - - - - - rs1253695 14:52395206 C 54331 NM_053064.4 Transcript intron_variant - - - - - - rs1253695 14:52395206 C ENSESTG00000011813 ENSESTT00000029632 Transcript intron_variant - - - - - - rs1253695 14:52395206 C ENSESTG00000011813 ENSESTT00000029642 Transcript intron_variant - - - - - - rs1253695 14:52395206 C 54331 NM_001243773.1 Transcript intron_variant - - - - - - rs1253695 14:52395206 C ENSESTG00000011813 ENSESTT00000029633 Transcript intron_variant - - - - - - rs1253680 14:52461386 C ENSESTG00000011828 ENSESTT00000029688 Transcript intron_variant - - - - - - rs1253680 14:52461386 C CCDS9705.1 CCDS9705.1 Transcript intron_variant - - - - - - rs1253680 14:52461386 C 51637 NM_016039.2 Transcript intron_variant - - - - - - rs1266398 14:52490321 C - ENSR00001457203 RegulatoryFeature regulatory_region_variant - - - - - - rs1266398 14:52490321 C CCDS9706.1 CCDS9706.1 Transcript intron_variant - - - - - - rs1266398 14:52490321 C 22795 NM_007361.3 Transcript intron_variant - - - - - - rs1266398 14:52490321 C ENSESTG00000011872 ENSESTT00000029778 Transcript intron_variant - - - - - - rs1266398 14:52490321 C ENSESTG00000011872 ENSESTT00000029779 Transcript intron_variant - - - - - - rs10132248 14:52573382 G - - - intergenic_variant - - - - - - rs10133895 14:52684467 A - - - intergenic_variant - - - - - - rs802960 14:52753787 A - - - intergenic_variant - - - - - - rs802959 14:52815558 C - ENSR00001457234 RegulatoryFeature regulatory_region_variant - - - - - - rs802959 14:52815558 C - - - intergenic_variant - - - - - - rs1033766 14:53141782 T CCDS9709.1 CCDS9709.1 Transcript intron_variant - - - - - - rs1033766 14:53141782 T ENSESTG00000006729 ENSESTT00000017080 Transcript intron_variant - - - - - - rs1033766 14:53141782 T ENSESTG00000006729 ENSESTT00000017075 Transcript intron_variant - - - - - - rs1033766 14:53141782 T 30001 NM_014584.1 Transcript intron_variant - - - - - - rs2357942 14:53167030 T CCDS9709.1 CCDS9709.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4831 rs2357942 14:53167030 T ENSESTG00000006729 ENSESTT00000017080 Transcript upstream_gene_variant - - - - - - DISTANCE=4568 rs2357942 14:53167030 T ENSESTG00000006729 ENSESTT00000017075 Transcript upstream_gene_variant - - - - - - DISTANCE=4568 rs2357942 14:53167030 T 30001 NM_014584.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4611 rs4898803 14:53849374 C ENSESTG00000000271 ENSESTT00000000651 Transcript intron_variant - - - - - - rs5021363 14:55111327 C CCDS32084.2 CCDS32084.2 Transcript intron_variant - - - - - - rs5021363 14:55111327 C CCDS55917.2 CCDS55917.2 Transcript intron_variant - - - - - - rs5021363 14:55111327 C 23034 NM_015589.5 Transcript intron_variant - - - - - - rs5021363 14:55111327 C 23034 NM_001161576.2 Transcript intron_variant - - - - - - rs2340922 14:55563793 C - - - intergenic_variant - - - - - - rs8016181 14:55741473 A - ENSR00001457493 RegulatoryFeature regulatory_region_variant - - - - - - rs8016181 14:55741473 A 55030 NM_152231.1 Transcript intron_variant - - - - - - rs8016181 14:55741473 A 55030 NM_017943.3 Transcript intron_variant - - - - - - rs8016181 14:55741473 A ENSESTG00000016608 ENSESTT00000041661 Transcript intron_variant - - - - - - rs7151729 14:55878636 C - ENSR00000097852 RegulatoryFeature regulatory_region_variant - - - - - - rs7151729 14:55878636 C CCDS32087.1 CCDS32087.1 Transcript upstream_gene_variant - - - - - - DISTANCE=96 rs7151729 14:55878636 C 387332 NM_199047.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2292 rs7151729 14:55878636 C 22863 NM_014924.4 Transcript upstream_gene_variant - - - - - - DISTANCE=60 rs7151729 14:55878636 C ENSESTG00000017066 ENSESTT00000042914 Transcript upstream_gene_variant - - - - - - DISTANCE=80 rs7151729 14:55878636 C CCDS9724.1 CCDS9724.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2461 rs10131125 14:56005520 T ENSESTG00000017059 ENSESTT00000042860 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042388 Transcript intron_variant - - - - - - rs4901595 14:56122613 A 3895 NM_004986.2 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042603 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042760 Transcript upstream_gene_variant - - - - - - DISTANCE=3767 rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042556 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042526 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042459 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042516 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042551 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042582 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042523 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042370 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042469 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042628 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042673 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042712 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042542 Transcript intron_variant - - - - - - rs4901595 14:56122613 A CCDS41959.1 CCDS41959.1 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042356 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042690 Transcript intron_variant - - - - - - rs4901595 14:56122613 A CCDS41957.1 CCDS41957.1 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042494 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042639 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042503 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042683 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042701 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042745 Transcript intron_variant - - - - - - rs4901595 14:56122613 A 3895 NM_001079521.1 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042723 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042509 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042570 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042403 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042731 Transcript intron_variant - - - - - - rs4901595 14:56122613 A 3895 NM_182926.2 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042655 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042592 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042420 Transcript intron_variant - - - - - - rs4901595 14:56122613 A 3895 NM_001079522.1 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042636 Transcript intron_variant - - - - - - rs4901595 14:56122613 A CCDS41958.1 CCDS41958.1 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042615 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042431 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042661 Transcript intron_variant - - - - - - rs4901595 14:56122613 A ENSESTG00000016718 ENSESTT00000042663 Transcript intron_variant - - - - - - rs2152285 14:56326724 T - - - intergenic_variant - - - - - - rs2150510 14:56369268 A - - - intergenic_variant - - - - - - rs1756638 14:56474984 T - - - intergenic_variant - - - - - - rs1189282 14:56948169 T - - - intergenic_variant - - - - - - rs1189274 14:56960009 T - - - intergenic_variant - - - - - - rs1556119 14:57123058 G - - - intergenic_variant - - - - - - rs1827654 14:57478729 C - - - intergenic_variant - - - - - - rs1957691 14:58142470 T 341880 NM_001206920.1 Transcript intron_variant - - - - - - rs2347358 14:58230221 T 341880 NM_001206920.1 Transcript intron_variant - - - - - - rs808215 14:58371911 A - - - intergenic_variant - - - - - - rs10133546 14:58761536 G ENSESTG00000022894 ENSESTT00000057978 Transcript upstream_gene_variant - - - - - - DISTANCE=3567 rs10133546 14:58761536 G 379025 NR_029435.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10133546 14:58761536 G ENSESTG00000023469 ENSESTT00000059233 Transcript intron_variant - - - - - - rs10133546 14:58761536 G ENSESTG00000023469 ENSESTT00000059176 Transcript intron_variant - - - - - - rs10133546 14:58761536 G 5926 NM_023000.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3686 rs10133546 14:58761536 G ENSESTG00000022894 ENSESTT00000057994 Transcript upstream_gene_variant - - - - - - DISTANCE=3770 rs10133546 14:58761536 G 5926 NM_023001.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3686 rs10133546 14:58761536 G ENSESTG00000023469 ENSESTT00000059265 Transcript intron_variant - - - - - - rs10133546 14:58761536 G 5926 NM_002892.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3686 rs10133546 14:58761536 G ENSESTG00000023469 ENSESTT00000059276 Transcript intron_variant - - - - - - rs10133546 14:58761536 G 379025 NR_029434.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10133546 14:58761536 G ENSESTG00000023469 ENSESTT00000059193 Transcript intron_variant - - - - - - rs10133546 14:58761536 G ENSESTG00000023469 ENSESTT00000059256 Transcript intron_variant - - - - - - rs10133546 14:58761536 G ENSESTG00000018640 ENSESTT00000046900 Transcript intron_variant - - - - - - rs1957037 14:58778432 A CCDS9732.1 CCDS9732.1 Transcript intron_variant - - - - - - rs1957037 14:58778432 A CCDS9733.1 CCDS9733.1 Transcript intron_variant - - - - - - rs1957037 14:58778432 A CCDS45114.1 CCDS45114.1 Transcript intron_variant - - - - - - rs1957037 14:58778432 A ENSESTG00000022894 ENSESTT00000057978 Transcript intron_variant - - - - - - rs1957037 14:58778432 A 5926 NM_023000.2 Transcript intron_variant - - - - - - rs1957037 14:58778432 A ENSESTG00000022894 ENSESTT00000057994 Transcript intron_variant - - - - - - rs1957037 14:58778432 A 5926 NM_023001.2 Transcript intron_variant - - - - - - rs1957037 14:58778432 A 5926 NM_002892.3 Transcript intron_variant - - - - - - rs2750123 14:59230445 T - - - intergenic_variant - - - - - - rs127397 14:59290420 C ENSESTG00000023384 ENSESTT00000059033 Transcript upstream_gene_variant - - - - - - DISTANCE=4586 rs127397 14:59290420 C ENSESTG00000023384 ENSESTT00000059020 Transcript upstream_gene_variant - - - - - - DISTANCE=4532 rs1252675 14:59375839 G ENSESTG00000023384 ENSESTT00000059033 Transcript intron_variant - - - - - - rs1252675 14:59375839 G ENSESTG00000023384 ENSESTT00000059020 Transcript intron_variant - - - - - - rs8022798 14:60947095 G 317761 NM_174978.2 Transcript intron_variant - - - - - - rs8022798 14:60947095 G ENSESTG00000002166 ENSESTT00000005403 Transcript intron_variant - - - - - - rs8022798 14:60947095 G ENSESTG00000002166 ENSESTT00000005409 Transcript intron_variant - - - - - - rs8022798 14:60947095 G CCDS9746.1 CCDS9746.1 Transcript intron_variant - - - - - - rs8020917 14:60952809 G - ENSR00001457807 RegulatoryFeature regulatory_region_variant - - - - - - rs8020917 14:60952809 G 317761 NM_174978.2 Transcript upstream_gene_variant - - - - - - DISTANCE=45 rs8020917 14:60952809 G ENSESTG00000002166 ENSESTT00000005403 Transcript upstream_gene_variant - - - - - - DISTANCE=47 rs8020917 14:60952809 G ENSESTG00000002166 ENSESTT00000005409 Transcript upstream_gene_variant - - - - - - DISTANCE=60 rs8020917 14:60952809 G CCDS9746.1 CCDS9746.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1013 rs1950318 14:61029336 C - - - intergenic_variant - - - - - - rs2145538 14:61295080 A CCDS53899.1 CCDS53899.1 Transcript intron_variant - - - - - - rs2145538 14:61295080 A 4331 NM_001177963.1 Transcript intron_variant - - - - - - rs2145538 14:61295080 A ENSESTG00000002089 ENSESTT00000005195 Transcript intron_variant - - - - - - rs2145538 14:61295080 A CCDS9750.1 CCDS9750.1 Transcript intron_variant - - - - - - rs2145538 14:61295080 A 4331 NM_002431.3 Transcript intron_variant - - - - - - rs7142228 14:61445967 G ENSESTG00000002122 ENSESTT00000005233 Transcript upstream_gene_variant - - - - - - DISTANCE=1871 rs7142228 14:61445967 G 145389 NM_001172702.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1865 rs7142228 14:61445967 G 145389 NR_033344.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1998 rs7142228 14:61445967 G CCDS53900.1 CCDS53900.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2029 rs7142228 14:61445967 G ENSESTG00000002146 ENSESTT00000005319 Transcript missense_variant 785 733 245 S/P Tct/Cct - rs7142228 14:61445967 G ENSESTG00000002122 ENSESTT00000005246 Transcript upstream_gene_variant - - - - - - DISTANCE=1876 rs7142228 14:61445967 G ENSESTG00000002122 ENSESTT00000005250 Transcript upstream_gene_variant - - - - - - DISTANCE=1984 rs7142228 14:61445967 G 145389 NM_153811.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1865 rs7142228 14:61445967 G CCDS9751.1 CCDS9751.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2029 rs7142228 14:61445967 G ENSESTG00000002122 ENSESTT00000005252 Transcript upstream_gene_variant - - - - - - DISTANCE=1997 rs7142228 14:61445967 G ENSESTG00000002122 ENSESTT00000005251 Transcript upstream_gene_variant - - - - - - DISTANCE=1988 rs7142228 14:61445967 G CCDS32092.1 CCDS32092.1 Transcript missense_variant 649 649 217 S/P Tct/Cct - PolyPhen=benign;SIFT=tolerated rs7142228 14:61445967 G ENSESTG00000002146 ENSESTT00000005332 Transcript missense_variant 737 649 217 S/P Tct/Cct - rs7142228 14:61445967 G ENSESTG00000002122 ENSESTT00000005249 Transcript upstream_gene_variant - - - - - - DISTANCE=1980 rs7142228 14:61445967 G 57570 NM_020810.2 Transcript missense_variant 740 649 217 S/P Tct/Cct - PolyPhen=benign;SIFT=tolerated rs1465143 14:61535822 A 145389 NM_001172702.1 Transcript intron_variant - - - - - - rs1465143 14:61535822 A 145389 NR_033344.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1465143 14:61535822 A CCDS53900.1 CCDS53900.1 Transcript intron_variant - - - - - - rs4902047 14:61791967 G ENSESTG00000019817 ENSESTT00000049874 Transcript upstream_gene_variant - - - - - - DISTANCE=1664 rs4902047 14:61791967 G ENSESTG00000019817 ENSESTT00000049834 Transcript intron_variant - - - - - - rs4902047 14:61791967 G ENSESTG00000019817 ENSESTT00000049867 Transcript upstream_gene_variant - - - - - - DISTANCE=1664 rs4902047 14:61791967 G 5583 NM_006255.3 Transcript intron_variant - - - - - - rs4902047 14:61791967 G ENSESTG00000020315 ENSESTT00000050976 Transcript upstream_gene_variant - - - - - - DISTANCE=2385 rs4902047 14:61791967 G ENSESTG00000019817 ENSESTT00000049746 Transcript intron_variant - - - - - - rs4902047 14:61791967 G ENSESTG00000020315 ENSESTT00000050999 Transcript upstream_gene_variant - - - - - - DISTANCE=2431 rs4902047 14:61791967 G ENSESTG00000019817 ENSESTT00000049846 Transcript intron_variant - - - - - - rs4902047 14:61791967 G CCDS9752.1 CCDS9752.1 Transcript intron_variant - - - - - - rs4902047 14:61791967 G ENSESTG00000019817 ENSESTT00000049858 Transcript intron_variant - - - - - - rs4902047 14:61791967 G ENSESTG00000019817 ENSESTT00000049851 Transcript intron_variant - - - - - - rs4902047 14:61791967 G ENSESTG00000019961 ENSESTT00000050045 Transcript intron_variant - - - - - - rs4902047 14:61791967 G ENSESTG00000019817 ENSESTT00000049820 Transcript intron_variant - - - - - - rs4902047 14:61791967 G ENSESTG00000019817 ENSESTT00000049872 Transcript upstream_gene_variant - - - - - - DISTANCE=1664 rs1254680 14:62238873 G CCDS9755.1 CCDS9755.1 Transcript intron_variant - - - - - - rs1254680 14:62238873 G 6617 NM_003082.3 Transcript intron_variant - - - - - - rs1473949 14:62768415 C - - - intergenic_variant - - - - - - rs1116050 14:62979515 C - - - intergenic_variant - - - - - - rs2029443 14:63088675 T - - - intergenic_variant - - - - - - rs181684 14:63253094 G 27133 NM_172376.1 Transcript intron_variant - - - - - - rs181684 14:63253094 G CCDS9756.1 CCDS9756.1 Transcript intron_variant - - - - - - rs181684 14:63253094 G 27133 NM_139318.3 Transcript intron_variant - - - - - - rs181684 14:63253094 G CCDS45123.1 CCDS45123.1 Transcript intron_variant - - - - - - rs181684 14:63253094 G CCDS45122.1 CCDS45122.1 Transcript intron_variant - - - - - - rs181684 14:63253094 G ENSESTG00000035758 ENSESTT00000090349 Transcript intron_variant - - - - - - rs181684 14:63253094 G 27133 NM_172375.1 Transcript intron_variant - - - - - - rs243143 14:63274813 A 27133 NM_172376.1 Transcript intron_variant - - - - - - rs243143 14:63274813 A CCDS9756.1 CCDS9756.1 Transcript intron_variant - - - - - - rs243143 14:63274813 A 27133 NM_139318.3 Transcript intron_variant - - - - - - rs243143 14:63274813 A CCDS45123.1 CCDS45123.1 Transcript intron_variant - - - - - - rs243143 14:63274813 A CCDS45122.1 CCDS45122.1 Transcript intron_variant - - - - - - rs243143 14:63274813 A 27133 NM_172375.1 Transcript intron_variant - - - - - - rs243142 14:63277262 T 27133 NM_172376.1 Transcript intron_variant - - - - - - rs243142 14:63277262 T CCDS9756.1 CCDS9756.1 Transcript intron_variant - - - - - - rs243142 14:63277262 T 27133 NM_139318.3 Transcript intron_variant - - - - - - rs243142 14:63277262 T CCDS45123.1 CCDS45123.1 Transcript intron_variant - - - - - - rs243142 14:63277262 T CCDS45122.1 CCDS45122.1 Transcript intron_variant - - - - - - rs243142 14:63277262 T 27133 NM_172375.1 Transcript intron_variant - - - - - - rs12886093 14:63452628 T ENSESTG00000035757 ENSESTT00000090348 Transcript intron_variant - - - - - - rs12886093 14:63452628 T 27133 NM_172376.1 Transcript intron_variant - - - - - - rs12886093 14:63452628 T ENSESTG00000035757 ENSESTT00000090347 Transcript intron_variant - - - - - - rs12886093 14:63452628 T 27133 NM_139318.3 Transcript intron_variant - - - - - - rs12886093 14:63452628 T CCDS9756.1 CCDS9756.1 Transcript intron_variant - - - - - - rs12886093 14:63452628 T ENSESTG00000035757 ENSESTT00000090346 Transcript intron_variant - - - - - - rs12886093 14:63452628 T CCDS45122.1 CCDS45122.1 Transcript intron_variant - - - - - - rs12886093 14:63452628 T CCDS45123.1 CCDS45123.1 Transcript intron_variant - - - - - - rs12886093 14:63452628 T 27133 NM_172375.1 Transcript intron_variant - - - - - - rs1956668 14:63533427 T 27133 NM_172376.1 Transcript intron_variant - - - - - - rs1956668 14:63533427 T ENSESTG00000035757 ENSESTT00000090347 Transcript intron_variant - - - - - - rs1956668 14:63533427 T ENSESTG00000035757 ENSESTT00000090346 Transcript intron_variant - - - - - - rs4902205 14:63598789 T ENSESTG00000035756 ENSESTT00000090344 Transcript upstream_gene_variant - - - - - - DISTANCE=3855 rs10142020 14:63625861 G - - - intergenic_variant - - - - - - rs1255716 14:64121256 G - ENSR00001024323 RegulatoryFeature regulatory_region_variant - - - - - - rs1255716 14:64121256 G - - - intergenic_variant - - - - - - rs2649197 14:65192122 G - ENSR00000419359 RegulatoryFeature regulatory_region_variant - - - - - - rs2649197 14:65192122 G ENSESTG00000024257 ENSESTT00000061316 Transcript intron_variant - - - - - - rs2649197 14:65192122 G ENSESTG00000024257 ENSESTT00000061379 Transcript intron_variant - - - - - - rs2649197 14:65192122 G ENSESTG00000024257 ENSESTT00000061394 Transcript intron_variant - - - - - - rs2649197 14:65192122 G 26030 NM_015549.1 Transcript intron_variant - - - - - - rs2649197 14:65192122 G ENSESTG00000024257 ENSESTT00000061357 Transcript intron_variant - - - - - - rs2649197 14:65192122 G CCDS32098.1 CCDS32098.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2228 rs7155142 14:65396801 A - ENSR00001458103 RegulatoryFeature regulatory_region_variant - - - - - - rs7155142 14:65396801 A ENSESTG00000024328 ENSESTT00000061644 Transcript intron_variant - - - - - - rs7155142 14:65396801 A 100529261 NM_001202559.1 Transcript intron_variant - - - - - - rs7155142 14:65396801 A 91612 NM_001204063.1 Transcript intron_variant - - - - - - rs7155142 14:65396801 A 100529261 NM_001202558.1 Transcript intron_variant - - - - - - rs7155142 14:65396801 A 91612 NM_001204064.1 Transcript intron_variant - - - - - - rs7155142 14:65396801 A 91612 NM_145165.3 Transcript intron_variant - - - - - - rs7155142 14:65396801 A ENSESTG00000024328 ENSESTT00000061535 Transcript intron_variant - - - - - - rs7155142 14:65396801 A ENSESTG00000024328 ENSESTT00000061636 Transcript intron_variant - - - - - - rs7155142 14:65396801 A ENSESTG00000024328 ENSESTT00000061656 Transcript intron_variant - - - - - - rs7155142 14:65396801 A ENSESTG00000024328 ENSESTT00000061653 Transcript intron_variant - - - - - - rs7155142 14:65396801 A CCDS55921.1 CCDS55921.1 Transcript intron_variant - - - - - - rs7155142 14:65396801 A ENSESTG00000024328 ENSESTT00000061622 Transcript intron_variant - - - - - - rs7155142 14:65396801 A CCDS55922.1 CCDS55922.1 Transcript intron_variant - - - - - - rs7155142 14:65396801 A CCDS32101.2 CCDS32101.2 Transcript intron_variant - - - - - - rs7160209 14:65589061 T - - - intergenic_variant - - - - - - rs8014558 14:65915059 C 2530 NR_038170.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8014558 14:65915059 C 2530 NM_178156.2 Transcript intron_variant - - - - - - rs8014558 14:65915059 C 2530 NM_178155.2 Transcript intron_variant - - - - - - rs8014558 14:65915059 C 2530 NM_004480.4 Transcript intron_variant - - - - - - rs8014558 14:65915059 C ENSESTG00000031518 ENSESTT00000079668 Transcript intron_variant - - - - - - rs8014558 14:65915059 C ENSESTG00000031518 ENSESTT00000079622 Transcript intron_variant - - - - - - rs8014558 14:65915059 C 2530 NR_038167.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2149838 14:65987841 A ENSESTG00000031518 ENSESTT00000079682 Transcript intron_variant - - - - - - rs2149838 14:65987841 A 2530 NM_178156.2 Transcript intron_variant - - - - - - rs2149838 14:65987841 A 2530 NM_004480.4 Transcript intron_variant - - - - - - rs2149838 14:65987841 A 2530 NR_038170.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2149838 14:65987841 A 2530 NM_178155.2 Transcript intron_variant - - - - - - rs2149838 14:65987841 A ENSESTG00000031518 ENSESTT00000079668 Transcript intron_variant - - - - - - rs2149838 14:65987841 A ENSESTG00000031518 ENSESTT00000079622 Transcript intron_variant - - - - - - rs2149838 14:65987841 A 2530 NR_038167.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9788554 14:66291517 G - ENSR00001458177 RegulatoryFeature regulatory_region_variant - - - - - - rs9788554 14:66291517 G - - - intergenic_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039666 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039648 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039622 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039610 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039585 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039689 Transcript intron_variant - - - - - - rs1274035 14:66999760 C 10243 NM_020806.4 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039697 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039663 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039665 Transcript intron_variant - - - - - - rs1274035 14:66999760 C CCDS32103.1 CCDS32103.1 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039568 Transcript intron_variant - - - - - - rs1274035 14:66999760 C CCDS9777.1 CCDS9777.1 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039538 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039588 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039692 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039660 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039641 Transcript intron_variant - - - - - - rs1274035 14:66999760 C 10243 NM_001024218.1 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039616 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039553 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039599 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039653 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039545 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039550 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039593 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039632 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039667 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039510 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039560 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039543 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039657 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039576 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039646 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039591 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039676 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039515 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039628 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039661 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039688 Transcript intron_variant - - - - - - rs1274035 14:66999760 C ENSESTG00000015738 ENSESTT00000039556 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039666 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039648 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039622 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039610 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039585 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039689 Transcript intron_variant - - - - - - rs7147533 14:67106740 A 10243 NM_020806.4 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039697 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039663 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039665 Transcript intron_variant - - - - - - rs7147533 14:67106740 A CCDS32103.1 CCDS32103.1 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039568 Transcript intron_variant - - - - - - rs7147533 14:67106740 A CCDS9777.1 CCDS9777.1 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039538 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039588 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039692 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039660 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039641 Transcript intron_variant - - - - - - rs7147533 14:67106740 A 10243 NM_001024218.1 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039616 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039553 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039599 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039653 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039545 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039550 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039593 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039632 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039667 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039510 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039560 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039543 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039657 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039576 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039646 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039591 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039676 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039515 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039628 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039661 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039688 Transcript intron_variant - - - - - - rs7147533 14:67106740 A ENSESTG00000015738 ENSESTT00000039556 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039666 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039648 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039622 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039610 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039585 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039689 Transcript intron_variant - - - - - - rs6573730 14:67353542 G 10243 NM_020806.4 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039704 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039697 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039663 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039665 Transcript intron_variant - - - - - - rs6573730 14:67353542 G CCDS32103.1 CCDS32103.1 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039568 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039699 Transcript intron_variant - - - - - - rs6573730 14:67353542 G CCDS9777.1 CCDS9777.1 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039538 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039588 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039692 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039660 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039641 Transcript intron_variant - - - - - - rs6573730 14:67353542 G 10243 NM_001024218.1 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039707 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039616 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039553 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039599 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039653 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039710 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039545 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039550 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039593 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039632 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039667 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039510 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039560 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039543 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039657 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039576 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039646 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039591 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039515 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039628 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039661 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039688 Transcript intron_variant - - - - - - rs6573730 14:67353542 G ENSESTG00000015738 ENSESTT00000039556 Transcript intron_variant - - - - - - rs1274319 14:67710606 C ENSESTG00000004365 ENSESTT00000011063 Transcript intron_variant - - - - - - rs1274319 14:67710606 C ENSESTG00000004365 ENSESTT00000011057 Transcript intron_variant - - - - - - rs1274319 14:67710606 C ENSESTG00000004365 ENSESTT00000011043 Transcript intron_variant - - - - - - rs1274319 14:67710606 C 64398 NM_022474.3 Transcript intron_variant - - - - - - rs1274319 14:67710606 C ENSESTG00000004365 ENSESTT00000011038 Transcript intron_variant - - - - - - rs1274319 14:67710606 C ENSESTG00000004365 ENSESTT00000011049 Transcript intron_variant - - - - - - rs1274319 14:67710606 C 64398 NM_001256550.1 Transcript intron_variant - - - - - - rs1274318 14:67712064 A ENSESTG00000004365 ENSESTT00000011063 Transcript intron_variant - - - - - - rs1274318 14:67712064 A ENSESTG00000004365 ENSESTT00000011057 Transcript intron_variant - - - - - - rs1274318 14:67712064 A ENSESTG00000004365 ENSESTT00000011043 Transcript intron_variant - - - - - - rs1274318 14:67712064 A 64398 NM_022474.3 Transcript intron_variant - - - - - - rs1274318 14:67712064 A ENSESTG00000004365 ENSESTT00000011038 Transcript intron_variant - - - - - - rs1274318 14:67712064 A ENSESTG00000004365 ENSESTT00000011049 Transcript intron_variant - - - - - - rs1274318 14:67712064 A 64398 NM_001256550.1 Transcript intron_variant - - - - - - rs911911 14:67761302 T CCDS58325.1 CCDS58325.1 Transcript intron_variant - - - - - - rs911911 14:67761302 T ENSESTG00000004365 ENSESTT00000011043 Transcript intron_variant - - - - - - rs911911 14:67761302 T 64398 NM_022474.3 Transcript intron_variant - - - - - - rs911911 14:67761302 T ENSESTG00000004365 ENSESTT00000011038 Transcript intron_variant - - - - - - rs911911 14:67761302 T CCDS9779.1 CCDS9779.1 Transcript intron_variant - - - - - - rs911911 14:67761302 T 64398 NM_001256550.1 Transcript intron_variant - - - - - - rs1315734 14:67936809 C ENSESTG00000004615 ENSESTT00000011629 Transcript downstream_gene_variant - - - - - - DISTANCE=3407 rs1315734 14:67936809 C CCDS9783.1 CCDS9783.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3328 rs1315734 14:67936809 C 161145 NM_182526.2 Transcript downstream_gene_variant - - - - - - DISTANCE=174 rs1315734 14:67936809 C ENSESTG00000004615 ENSESTT00000011631 Transcript downstream_gene_variant - - - - - - DISTANCE=3407 rs1315734 14:67936809 C ENSESTG00000004615 ENSESTT00000011626 Transcript downstream_gene_variant - - - - - - DISTANCE=3407 rs1950765 14:68327341 G ENSESTG00000004511 ENSESTT00000011416 Transcript intron_variant - - - - - - rs1950765 14:68327341 G CCDS9790.1 CCDS9790.1 Transcript intron_variant - - - - - - rs1950765 14:68327341 G ENSESTG00000004511 ENSESTT00000011421 Transcript intron_variant - - - - - - rs1950765 14:68327341 G CCDS9789.1 CCDS9789.1 Transcript intron_variant - - - - - - rs1950765 14:68327341 G 5890 NM_133510.3 Transcript intron_variant - - - - - - rs1950765 14:68327341 G 5890 NM_133509.3 Transcript intron_variant - - - - - - rs1950765 14:68327341 G 5890 NM_002877.5 Transcript intron_variant - - - - - - rs6573799 14:68329216 A ENSESTG00000004511 ENSESTT00000011416 Transcript intron_variant - - - - - - rs6573799 14:68329216 A CCDS9790.1 CCDS9790.1 Transcript intron_variant - - - - - - rs6573799 14:68329216 A ENSESTG00000004511 ENSESTT00000011421 Transcript intron_variant - - - - - - rs6573799 14:68329216 A CCDS9789.1 CCDS9789.1 Transcript intron_variant - - - - - - rs6573799 14:68329216 A 5890 NM_133510.3 Transcript intron_variant - - - - - - rs6573799 14:68329216 A 5890 NM_133509.3 Transcript intron_variant - - - - - - rs6573799 14:68329216 A 5890 NM_002877.5 Transcript intron_variant - - - - - - rs2103962 14:68417863 C CCDS9790.1 CCDS9790.1 Transcript intron_variant - - - - - - rs2103962 14:68417863 C CCDS9789.1 CCDS9789.1 Transcript intron_variant - - - - - - rs2103962 14:68417863 C 5890 NM_133510.3 Transcript intron_variant - - - - - - rs2103962 14:68417863 C 5890 NM_133509.3 Transcript intron_variant - - - - - - rs2103962 14:68417863 C 5890 NM_002877.5 Transcript intron_variant - - - - - - rs429635 14:68593801 A CCDS9790.1 CCDS9790.1 Transcript intron_variant - - - - - - rs429635 14:68593801 A CCDS9789.1 CCDS9789.1 Transcript intron_variant - - - - - - rs429635 14:68593801 A 5890 NM_133510.3 Transcript intron_variant - - - - - - rs429635 14:68593801 A 5890 NM_133509.3 Transcript intron_variant - - - - - - rs429635 14:68593801 A 5890 NM_002877.5 Transcript intron_variant - - - - - - rs4902575 14:68859769 G CCDS9790.1 CCDS9790.1 Transcript intron_variant - - - - - - rs4902575 14:68859769 G CCDS9789.1 CCDS9789.1 Transcript intron_variant - - - - - - rs4902575 14:68859769 G 5890 NM_133510.3 Transcript intron_variant - - - - - - rs4902575 14:68859769 G ENSESTG00000007396 ENSESTT00000018623 Transcript intron_variant - - - - - - rs4902575 14:68859769 G 5890 NM_133509.3 Transcript intron_variant - - - - - - rs4902575 14:68859769 G 5890 NM_002877.5 Transcript intron_variant - - - - - - rs2525528 14:69011832 C ENSESTG00000007419 ENSESTT00000018663 Transcript upstream_gene_variant - - - - - - DISTANCE=447 rs2525528 14:69011832 C CCDS9789.1 CCDS9789.1 Transcript intron_variant - - - - - - rs2525528 14:69011832 C 5890 NM_133509.3 Transcript intron_variant - - - - - - rs1290998 14:69044539 G - ENSR00000419887 RegulatoryFeature regulatory_region_variant - - - - - - rs1290998 14:69044539 G ENSESTG00000007419 ENSESTT00000018663 Transcript intron_variant - - - - - - rs1290998 14:69044539 G CCDS9789.1 CCDS9789.1 Transcript intron_variant - - - - - - rs1290998 14:69044539 G 5890 NM_133509.3 Transcript intron_variant - - - - - - rs424855 14:69185763 C - - - intergenic_variant - - - - - - rs1275203 14:69481922 C - ENSR00001458423 RegulatoryFeature regulatory_region_variant - - - - - - rs1275203 14:69481922 C ENSESTG00000007640 ENSESTT00000019245 Transcript intron_variant - - - - - - rs9743448 14:69633430 A ENSESTG00000030424 ENSESTT00000076555 Transcript intron_variant - - - - - - rs11845360 14:69664858 A ENSESTG00000029890 ENSESTT00000075308 Transcript intron_variant - - - - - - rs11845360 14:69664858 A 55218 NM_018199.3 Transcript intron_variant - - - - - - rs11845360 14:69664858 A 55218 NM_001193362.1 Transcript intron_variant - - - - - - rs11845360 14:69664858 A 55218 NM_001193361.1 Transcript intron_variant - - - - - - rs11845360 14:69664858 A ENSESTG00000029890 ENSESTT00000075375 Transcript intron_variant - - - - - - rs11845360 14:69664858 A ENSESTG00000029890 ENSESTT00000075334 Transcript intron_variant - - - - - - rs11845360 14:69664858 A 55218 NR_034165.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11845360 14:69664858 A ENSESTG00000029890 ENSESTT00000075366 Transcript intron_variant - - - - - - rs11845360 14:69664858 A 55218 NM_001193363.1 Transcript intron_variant - - - - - - rs11845360 14:69664858 A 55218 NM_001193360.1 Transcript intron_variant - - - - - - rs11845360 14:69664858 A 55218 NR_034164.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8004261 14:69679834 T ENSESTG00000029890 ENSESTT00000075308 Transcript intron_variant - - - - - - rs8004261 14:69679834 T 55218 NM_018199.3 Transcript intron_variant - - - - - - rs8004261 14:69679834 T 55218 NM_001193362.1 Transcript intron_variant - - - - - - rs8004261 14:69679834 T 55218 NM_001193361.1 Transcript intron_variant - - - - - - rs8004261 14:69679834 T ENSESTG00000029890 ENSESTT00000075375 Transcript intron_variant - - - - - - rs8004261 14:69679834 T ENSESTG00000029890 ENSESTT00000075334 Transcript intron_variant - - - - - - rs8004261 14:69679834 T CCDS53902.1 CCDS53902.1 Transcript intron_variant - - - - - - rs8004261 14:69679834 T 55218 NR_034165.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8004261 14:69679834 T ENSESTG00000029890 ENSESTT00000075366 Transcript intron_variant - - - - - - rs8004261 14:69679834 T 55218 NM_001193363.1 Transcript intron_variant - - - - - - rs8004261 14:69679834 T 55218 NM_001193360.1 Transcript intron_variant - - - - - - rs8004261 14:69679834 T 55218 NR_034164.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1295823 14:69975665 T ENSESTG00000030171 ENSESTT00000075927 Transcript intron_variant - - - - - - rs1295823 14:69975665 T CCDS53903.1 CCDS53903.1 Transcript intron_variant - - - - - - rs1295823 14:69975665 T 400224 NM_001161498.1 Transcript intron_variant - - - - - - rs7151315 14:70326880 G - - - intergenic_variant - - - - - - rs227413 14:70460693 T ENSESTG00000030247 ENSESTT00000076244 Transcript intron_variant - - - - - - rs227413 14:70460693 T 64093 NM_001034852.2 Transcript intron_variant - - - - - - rs227413 14:70460693 T ENSESTG00000030247 ENSESTT00000076257 Transcript intron_variant - - - - - - rs227413 14:70460693 T CCDS9798.1 CCDS9798.1 Transcript intron_variant - - - - - - rs227413 14:70460693 T CCDS32110.1 CCDS32110.1 Transcript intron_variant - - - - - - rs227413 14:70460693 T 64093 NM_022137.5 Transcript intron_variant - - - - - - rs55981023 14:70762402 G - - - intergenic_variant - - - - - - rs4902818 14:70888026 C ENSESTG00000000244 ENSESTT00000000606 Transcript upstream_gene_variant - - - - - - DISTANCE=4220 rs4902818 14:70888026 C 55333 NM_018373.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4219 rs4902818 14:70888026 C ENSESTG00000000209 ENSESTT00000000516 Transcript intron_variant - - - - - - rs4902818 14:70888026 C 100529257 NM_001202548.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4219 rs4902818 14:70888026 C 100529257 NM_001202547.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4219 rs4902818 14:70888026 C CCDS9803.1 CCDS9803.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4346 rs4902818 14:70888026 C 100529257 NM_001202549.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4219 rs8007357 14:70911546 T ENSESTG00000000209 ENSESTT00000000516 Transcript intron_variant - - - - - - rs10132724 14:71121775 G - ENSR00000180801 RegulatoryFeature regulatory_region_variant - - - - - - rs10132724 14:71121775 G CCDS45132.1 CCDS45132.1 Transcript intron_variant - - - - - - rs10132724 14:71121775 G ENSESTG00000000214 ENSESTT00000000528 Transcript intron_variant - - - - - - rs10132724 14:71121775 G 23508 NM_015351.1 Transcript intron_variant - - - - - - rs10140837 14:71311976 T - - - intergenic_variant - - - - - - rs1859467 14:71408631 G CCDS9806.1 CCDS9806.1 Transcript intron_variant - - - - - - rs1859467 14:71408631 G 22990 NM_014982.2 Transcript intron_variant - - - - - - rs2810094 14:71438340 A CCDS9806.1 CCDS9806.1 Transcript intron_variant - - - - - - rs2810094 14:71438340 A 22990 NM_014982.2 Transcript intron_variant - - - - - - rs2810094 14:71438340 A ENSESTG00000000223 ENSESTT00000000551 Transcript intron_variant - - - - - - rs4902875 14:71525954 A CCDS9806.1 CCDS9806.1 Transcript intron_variant - - - - - - rs4902875 14:71525954 A 22990 NM_014982.2 Transcript intron_variant - - - - - - rs4902875 14:71525954 A ENSESTG00000000232 ENSESTT00000000577 Transcript intron_variant - - - - - - rs2332578 14:71872032 A ENSESTG00000024568 ENSESTT00000062080 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_001204418.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_001204421.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_001204424.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G CCDS55924.1 CCDS55924.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G CCDS55925.1 CCDS55925.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_001204416.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_001204420.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_001204422.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_001204417.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_004296.5 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_001204423.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G CCDS9808.1 CCDS9808.1 Transcript intron_variant - - - - - - rs2529473 14:72807182 G 9628 NM_001204419.1 Transcript intron_variant - - - - - - rs2526925 14:73097058 G - - - intergenic_variant - - - - - - rs4903058 14:73248557 G - ENSR00001458702 RegulatoryFeature regulatory_region_variant - - - - - - rs4903058 14:73248557 G 8110 NM_012074.3 Transcript intron_variant - - - - - - rs4903058 14:73248557 G ENSESTG00000017187 ENSESTT00000043162 Transcript intron_variant - - - - - - rs4903058 14:73248557 G ENSESTG00000017187 ENSESTT00000043177 Transcript intron_variant - - - - - - rs4903058 14:73248557 G CCDS45133.1 CCDS45133.1 Transcript intron_variant - - - - - - rs4903058 14:73248557 G ENSESTG00000017187 ENSESTT00000043166 Transcript intron_variant - - - - - - rs214295 14:73550944 A 58517 NM_021239.2 Transcript intron_variant - - - - - - rs214295 14:73550944 A ENSESTG00000012494 ENSESTT00000031355 Transcript upstream_gene_variant - - - - - - DISTANCE=3759 rs214295 14:73550944 A ENSESTG00000017071 ENSESTT00000042943 Transcript intron_variant - - - - - - rs214295 14:73550944 A ENSESTG00000017071 ENSESTT00000042933 Transcript intron_variant - - - - - - rs214295 14:73550944 A ENSESTG00000017071 ENSESTT00000042897 Transcript intron_variant - - - - - - rs214295 14:73550944 A ENSESTG00000017071 ENSESTT00000042950 Transcript downstream_gene_variant - - - - - - DISTANCE=673 rs214295 14:73550944 A CCDS32113.1 CCDS32113.1 Transcript intron_variant - - - - - - rs214295 14:73550944 A ENSESTG00000012494 ENSESTT00000031357 Transcript upstream_gene_variant - - - - - - DISTANCE=3759 rs7158040 14:74022738 G ENSESTG00000012593 ENSESTT00000031581 Transcript intron_variant - - - - - - rs7158040 14:74022738 G ENSESTG00000012829 ENSESTT00000032175 Transcript intron_variant - - - - - - rs7158040 14:74022738 G ENSESTG00000012593 ENSESTT00000031607 Transcript intron_variant - - - - - - rs7158040 14:74022738 G 399671 NM_203309.2 Transcript intron_variant - - - - - - rs7158040 14:74022738 G 399671 NM_001220484.1 Transcript intron_variant - - - - - - rs12880771 14:74023794 A ENSESTG00000012593 ENSESTT00000031581 Transcript intron_variant - - - - - - rs12880771 14:74023794 A ENSESTG00000012829 ENSESTT00000032175 Transcript intron_variant - - - - - - rs12880771 14:74023794 A ENSESTG00000012593 ENSESTT00000031607 Transcript intron_variant - - - - - - rs12880771 14:74023794 A 399671 NM_203309.2 Transcript intron_variant - - - - - - rs12880771 14:74023794 A 399671 NM_001220484.1 Transcript intron_variant - - - - - - rs11159033 14:74120745 C CCDS45134.1 CCDS45134.1 Transcript intron_variant - - - - - - rs11159033 14:74120745 C CCDS55928.1 CCDS55928.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4880 rs11159033 14:74120745 C 83544 NM_001201366.1 Transcript intron_variant - - - - - - rs11159033 14:74120745 C ENSESTG00000012628 ENSESTT00000031661 Transcript intron_variant - - - - - - rs11159033 14:74120745 C ENSESTG00000012628 ENSESTT00000031659 Transcript intron_variant - - - - - - rs11159033 14:74120745 C 83544 NM_031427.3 Transcript intron_variant - - - - - - rs2108762 14:74252966 C - ENSR00000180913 RegulatoryFeature regulatory_region_variant - - - - - - rs2108762 14:74252966 C ENSESTG00000012817 ENSESTT00000032151 Transcript intron_variant - - - - - - rs2108762 14:74252966 C ENSESTG00000012817 ENSESTT00000032147 Transcript intron_variant - - - - - - rs2108762 14:74252966 C ENSESTG00000012640 ENSESTT00000031686 Transcript upstream_gene_variant - - - - - - DISTANCE=1097 rs2108762 14:74252966 C 91748 NM_001043318.1 Transcript intron_variant - - - - - - rs4903210 14:74700204 C - - - intergenic_variant - - - - - - rs4903226 14:74920983 C - - - intergenic_variant - - - - - - rs8011417 14:75098759 G - - - intergenic_variant - - - - - - rs10146493 14:75125322 T 9870 NM_001039479.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2633 rs7149057 14:75158350 A ENSESTG00000014173 ENSESTT00000035499 Transcript intron_variant - - - - - - rs7149057 14:75158350 A 9870 NM_001039479.1 Transcript intron_variant - - - - - - rs8005569 14:75171630 C ENSESTG00000014173 ENSESTT00000035499 Transcript intron_variant - - - - - - rs8005569 14:75171630 C 9870 NM_001039479.1 Transcript intron_variant - - - - - - rs10151476 14:75209890 G - - - intergenic_variant - - - - - - rs175005 14:75445360 G - - - intergenic_variant - - - - - - rs175456 14:75585075 C CCDS9839.1 CCDS9839.1 Transcript intron_variant - - - - - - rs175456 14:75585075 C 91754 NM_033116.4 Transcript intron_variant - - - - - - rs175428 14:75616449 T ENSESTG00000020378 ENSESTT00000051263 Transcript intron_variant - - - - - - rs175428 14:75616449 T CCDS9840.1 CCDS9840.1 Transcript intron_variant - - - - - - rs175428 14:75616449 T 10972 NM_006827.5 Transcript intron_variant - - - - - - rs2014376 14:75784587 T - - - intergenic_variant - - - - - - rs175695 14:75954364 G - ENSR00000421049 RegulatoryFeature regulatory_region_variant - - - - - - rs175695 14:75954364 G - - - intergenic_variant - - - - - - rs759706 14:76574734 C - - - intergenic_variant - - - - - - rs1900123 14:76629670 A 55668 NM_017972.2 Transcript intron_variant - - - - - - rs1900123 14:76629670 A CCDS9848.1 CCDS9848.1 Transcript intron_variant - - - - - - rs1900123 14:76629670 A 55668 NM_017926.2 Transcript intron_variant - - - - - - rs1900123 14:76629670 A CCDS9849.1 CCDS9849.1 Transcript intron_variant - - - - - - rs2885250 14:76865949 C ENSESTG00000024403 ENSESTT00000061726 Transcript intron_variant - - - - - - rs2885250 14:76865949 C 2103 NM_004452.3 Transcript intron_variant - - - - - - rs2980891 14:76954008 G 2103 NM_004452.3 Transcript intron_variant - - - - - - rs2980891 14:76954008 G CCDS9850.2 CCDS9850.2 Transcript intron_variant - - - - - - rs1676242 14:76996753 G - - - intergenic_variant - - - - - - rs1625096 14:77013966 G - - - intergenic_variant - - - - - - rs6574318 14:77177403 G ENSESTG00000024429 ENSESTT00000061757 Transcript upstream_gene_variant - - - - - - DISTANCE=2847 rs8017527 14:77208777 A - - - intergenic_variant - - - - - - rs759594 14:77425070 C - ENSR00000421261 RegulatoryFeature regulatory_region_variant - - - - - - rs759594 14:77425070 C - - - intergenic_variant - - - - - - rs2655979 14:77604997 G 283576 NM_174976.2 Transcript intron_variant - - - - - - rs2655979 14:77604997 G ENSESTG00000030121 ENSESTT00000075930 Transcript intron_variant - - - - - - rs2655979 14:77604997 G CCDS45140.1 CCDS45140.1 Transcript intron_variant - - - - - - rs2655979 14:77604997 G ENSESTG00000030121 ENSESTT00000075899 Transcript intron_variant - - - - - - rs4903553 14:77644391 G ENSESTG00000030121 ENSESTT00000075971 Transcript upstream_gene_variant - - - - - - DISTANCE=3761 rs4903553 14:77644391 G ENSESTG00000030121 ENSESTT00000075978 Transcript upstream_gene_variant - - - - - - DISTANCE=3779 rs4903553 14:77644391 G 57156 NM_020431.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3711 rs4903553 14:77644391 G ENSESTG00000030121 ENSESTT00000075991 Transcript upstream_gene_variant - - - - - - DISTANCE=3779 rs4903553 14:77644391 G ENSESTG00000030121 ENSESTT00000075944 Transcript intron_variant - - - - - - rs4903553 14:77644391 G ENSESTG00000030121 ENSESTT00000075930 Transcript intron_variant - - - - - - rs4903553 14:77644391 G ENSESTG00000030121 ENSESTT00000075899 Transcript intron_variant - - - - - - rs4903554 14:77644469 G ENSESTG00000030121 ENSESTT00000075971 Transcript upstream_gene_variant - - - - - - DISTANCE=3683 rs4903554 14:77644469 G ENSESTG00000030121 ENSESTT00000075978 Transcript upstream_gene_variant - - - - - - DISTANCE=3701 rs4903554 14:77644469 G 57156 NM_020431.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3633 rs4903554 14:77644469 G ENSESTG00000030121 ENSESTT00000075991 Transcript upstream_gene_variant - - - - - - DISTANCE=3701 rs4903554 14:77644469 G ENSESTG00000030121 ENSESTT00000075944 Transcript intron_variant - - - - - - rs4903554 14:77644469 G ENSESTG00000030121 ENSESTT00000075930 Transcript intron_variant - - - - - - rs4903554 14:77644469 G ENSESTG00000030121 ENSESTT00000075899 Transcript intron_variant - - - - - - rs2655992 14:77645127 A ENSESTG00000030121 ENSESTT00000075971 Transcript upstream_gene_variant - - - - - - DISTANCE=3025 rs2655992 14:77645127 A ENSESTG00000030121 ENSESTT00000075978 Transcript upstream_gene_variant - - - - - - DISTANCE=3043 rs2655992 14:77645127 A 57156 NM_020431.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2975 rs2655992 14:77645127 A ENSESTG00000030121 ENSESTT00000075991 Transcript upstream_gene_variant - - - - - - DISTANCE=3043 rs2655992 14:77645127 A ENSESTG00000030121 ENSESTT00000075944 Transcript intron_variant - - - - - - rs2655992 14:77645127 A ENSESTG00000030121 ENSESTT00000075930 Transcript intron_variant - - - - - - rs2655992 14:77645127 A ENSESTG00000030121 ENSESTT00000075899 Transcript intron_variant - - - - - - rs1508300 14:77654023 G - ENSR00001024524 RegulatoryFeature regulatory_region_variant - - - - - - rs1508300 14:77654023 G ENSESTG00000030121 ENSESTT00000075971 Transcript intron_variant - - - - - - rs1508300 14:77654023 G ENSESTG00000030121 ENSESTT00000075978 Transcript intron_variant - - - - - - rs1508300 14:77654023 G 57156 NM_020431.2 Transcript intron_variant - - - - - - rs1508300 14:77654023 G ENSESTG00000030121 ENSESTT00000075991 Transcript intron_variant - - - - - - rs1508300 14:77654023 G ENSESTG00000030121 ENSESTT00000075944 Transcript intron_variant - - - - - - rs1508300 14:77654023 G ENSESTG00000030121 ENSESTT00000075930 Transcript intron_variant - - - - - - rs1508300 14:77654023 G ENSESTG00000030121 ENSESTT00000075899 Transcript intron_variant - - - - - - rs375566 14:77697967 G ENSESTG00000030121 ENSESTT00000075978 Transcript synonymous_variant 531 387 129 A gcA/gcG - rs375566 14:77697967 G 57156 NM_020431.2 Transcript synonymous_variant 599 387 129 A gcA/gcG - rs375566 14:77697967 G CCDS45141.1 CCDS45141.1 Transcript synonymous_variant 387 387 129 A gcA/gcG - rs375566 14:77697967 G ENSESTG00000030121 ENSESTT00000075899 Transcript downstream_gene_variant - - - - - - DISTANCE=11 rs4479155 14:78120104 C - ENSR00000421390 RegulatoryFeature regulatory_region_variant - - - - - - rs4479155 14:78120104 C - - - intergenic_variant - - - - - - rs8018423 14:78611925 C - - - intergenic_variant - - - - - - rs7158022 14:78724713 T - - - intergenic_variant - - - - - - rs717108 14:78926459 G ENSESTG00000015588 ENSESTT00000039037 Transcript intron_variant - - - - - - rs717108 14:78926459 G ENSESTG00000015588 ENSESTT00000039047 Transcript intron_variant - - - - - - rs717108 14:78926459 G 9369 NM_004796.4 Transcript intron_variant - - - - - - rs6574448 14:78945520 G ENSESTG00000015588 ENSESTT00000039037 Transcript intron_variant - - - - - - rs6574448 14:78945520 G ENSESTG00000015588 ENSESTT00000039047 Transcript intron_variant - - - - - - rs6574448 14:78945520 G 9369 NM_004796.4 Transcript intron_variant - - - - - - rs8007816 14:79097721 G ENSESTG00000015588 ENSESTT00000039056 Transcript intron_variant - - - - - - rs8007816 14:79097721 G ENSESTG00000015588 ENSESTT00000039037 Transcript intron_variant - - - - - - rs8007816 14:79097721 G ENSESTG00000015588 ENSESTT00000039047 Transcript intron_variant - - - - - - rs8007816 14:79097721 G 9369 NM_004796.4 Transcript intron_variant - - - - - - rs10132461 14:79263263 T ENSESTG00000015588 ENSESTT00000039037 Transcript intron_variant - - - - - - rs10132461 14:79263263 T 9369 NM_004796.4 Transcript intron_variant - - - - - - rs10132461 14:79263263 T CCDS9870.1 CCDS9870.1 Transcript intron_variant - - - - - - rs10132461 14:79263263 T ENSESTG00000015588 ENSESTT00000039063 Transcript intron_variant - - - - - - rs10132461 14:79263263 T ENSESTG00000015588 ENSESTT00000039078 Transcript intron_variant - - - - - - rs8022835 14:79281076 T ENSESTG00000015588 ENSESTT00000039037 Transcript intron_variant - - - - - - rs8022835 14:79281076 T 9369 NM_004796.4 Transcript intron_variant - - - - - - rs8022835 14:79281076 T CCDS9870.1 CCDS9870.1 Transcript intron_variant - - - - - - rs8022835 14:79281076 T ENSESTG00000015588 ENSESTT00000039063 Transcript intron_variant - - - - - - rs8022835 14:79281076 T ENSESTG00000015588 ENSESTT00000039078 Transcript intron_variant - - - - - - rs1184261 14:79437515 C 9369 NM_004796.4 Transcript intron_variant - - - - - - rs1184261 14:79437515 C CCDS9870.1 CCDS9870.1 Transcript intron_variant - - - - - - rs1184261 14:79437515 C ENSESTG00000015588 ENSESTT00000039078 Transcript downstream_gene_variant - - - - - - DISTANCE=2892 rs10131560 14:79576227 T 9369 NM_004796.4 Transcript intron_variant - - - - - - rs10131560 14:79576227 T CCDS9870.1 CCDS9870.1 Transcript intron_variant - - - - - - rs2199795 14:79627736 C 9369 NM_004796.4 Transcript intron_variant - - - - - - rs2199795 14:79627736 C CCDS9870.1 CCDS9870.1 Transcript intron_variant - - - - - - rs1531624 14:79684602 G 9369 NM_004796.4 Transcript intron_variant - - - - - - rs1531624 14:79684602 G CCDS9870.1 CCDS9870.1 Transcript intron_variant - - - - - - rs61995414 14:79723989 A - ENSR00000652391 RegulatoryFeature regulatory_region_variant - - - - - - rs61995414 14:79723989 A 9369 NM_004796.4 Transcript intron_variant - - - - - - rs61995414 14:79723989 A CCDS9870.1 CCDS9870.1 Transcript intron_variant - - - - - - rs4903877 14:80241146 A ENSESTG00000035030 ENSESTT00000088537 Transcript intron_variant - - - - - - rs4903877 14:80241146 A CCDS45145.1 CCDS45145.1 Transcript intron_variant - - - - - - rs4903877 14:80241146 A ENSESTG00000035020 ENSESTT00000088518 Transcript intron_variant - - - - - - rs4903877 14:80241146 A ENSESTG00000035020 ENSESTT00000088522 Transcript intron_variant - - - - - - rs4903877 14:80241146 A 9369 NM_138970.3 Transcript intron_variant - - - - - - rs4903877 14:80241146 A 9369 NM_004796.4 Transcript intron_variant - - - - - - rs4903877 14:80241146 A CCDS9870.1 CCDS9870.1 Transcript intron_variant - - - - - - rs4903877 14:80241146 A CCDS9871.1 CCDS9871.1 Transcript intron_variant - - - - - - rs4903877 14:80241146 A 9369 NM_001105250.1 Transcript intron_variant - - - - - - rs6574614 14:81408133 C - ENSR00001459216 RegulatoryFeature regulatory_region_variant - - - - - - rs6574614 14:81408133 C ENSESTG00000015546 ENSESTT00000038937 Transcript synonymous_variant 199 54 18 P ccG/ccC - rs6574614 14:81408133 C 145508 NM_152446.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2249 rs6574614 14:81408133 C ENSESTG00000015595 ENSESTT00000039110 Transcript upstream_gene_variant - - - - - - DISTANCE=64 rs6574614 14:81408133 C ENSESTG00000015595 ENSESTT00000039064 Transcript upstream_gene_variant - - - - - - DISTANCE=50 rs2888086 14:81638637 G - ENSR00001459238 RegulatoryFeature regulatory_region_variant - - - - - - rs2888086 14:81638637 G 2957 NM_201595.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3159 rs2888086 14:81638637 G 2957 NR_048573.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3159 rs2888086 14:81638637 G 2957 NM_015859.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3159 rs1210794 14:81758484 T CCDS58332.1 CCDS58332.1 Transcript intron_variant - - - - - - rs1210794 14:81758484 T 85439 NM_033104.3 Transcript intron_variant - - - - - - rs1210794 14:81758484 T 85439 NM_001256430.1 Transcript intron_variant - - - - - - rs1210794 14:81758484 T ENSESTG00000026796 ENSESTT00000067532 Transcript intron_variant - - - - - - rs1210794 14:81758484 T CCDS9875.1 CCDS9875.1 Transcript intron_variant - - - - - - rs1210794 14:81758484 T ENSESTG00000026796 ENSESTT00000067561 Transcript intron_variant - - - - - - rs2719819 14:81777565 G CCDS58332.1 CCDS58332.1 Transcript intron_variant - - - - - - rs2719819 14:81777565 G 85439 NM_033104.3 Transcript intron_variant - - - - - - rs2719819 14:81777565 G 85439 NM_001256430.1 Transcript intron_variant - - - - - - rs2719819 14:81777565 G ENSESTG00000026796 ENSESTT00000067532 Transcript intron_variant - - - - - - rs2719819 14:81777565 G CCDS9875.1 CCDS9875.1 Transcript intron_variant - - - - - - rs2719819 14:81777565 G ENSESTG00000026796 ENSESTT00000067561 Transcript intron_variant - - - - - - rs1242522 14:83193373 A - - - intergenic_variant - - - - - - rs6574720 14:83284176 A - - - intergenic_variant - - - - - - rs2372530 14:84227530 G - - - intergenic_variant - - - - - - rs1159336 14:84657934 A ENSESTG00000035201 ENSESTT00000088922 Transcript intron_variant - - - - - - rs982109 14:84670087 G ENSESTG00000035201 ENSESTT00000088922 Transcript intron_variant - - - - - - rs982108 14:84670237 T ENSESTG00000035201 ENSESTT00000088922 Transcript intron_variant - - - - - - rs4454898 14:84792027 C - - - intergenic_variant - - - - - - rs4904173 14:84832703 T - - - intergenic_variant - - - - - - rs2816007 14:84858000 A - - - intergenic_variant - - - - - - rs2998302 14:85001188 A - - - intergenic_variant - - - - - - rs4904232 14:85527096 A - - - intergenic_variant - - - - - - rs2372863 14:85551025 A - - - intergenic_variant - - - - - - rs1767419 14:85653819 A - - - intergenic_variant - - - - - - rs6574820 14:85894008 T ENSESTG00000019297 ENSESTT00000048475 Transcript intron_variant - - - - - - rs10134815 14:86125162 A - - - intergenic_variant - - - - - - rs1543469 14:86143049 G - - - intergenic_variant - - - - - - rs7150201 14:86535515 C ENSESTG00000033867 ENSESTT00000085615 Transcript intron_variant - - - - - - rs7150201 14:86535515 C ENSESTG00000019235 ENSESTT00000048360 Transcript intron_variant - - - - - - rs7150201 14:86535515 C ENSESTG00000019235 ENSESTT00000048342 Transcript intron_variant - - - - - - rs7150201 14:86535515 C ENSESTG00000033867 ENSESTT00000085616 Transcript upstream_gene_variant - - - - - - DISTANCE=1583 rs994323 14:86755913 G - - - intergenic_variant - - - - - - rs2802071 14:87307414 G - - - intergenic_variant - - - - - - rs1642206 14:87491598 A - - - intergenic_variant - - - - - - rs2244653 14:87751481 C - - - intergenic_variant - - - - - - rs408755 14:87753347 G - ENSR00000422076 RegulatoryFeature regulatory_region_variant - - - - - - rs408755 14:87753347 G - - - intergenic_variant - - - - - - rs6574936 14:87838297 G - - - intergenic_variant - - - - - - rs4904381 14:87865407 T - - - intergenic_variant - - - - - - rs4904382 14:87865426 G - - - intergenic_variant - - - - - - rs2478185 14:87899288 C - - - intergenic_variant - - - - - - rs2246377 14:87903110 C - - - intergenic_variant - - - - - - rs8011395 14:87957207 C - - - intergenic_variant - - - - - - rs1951503 14:87976548 C - - - intergenic_variant - - - - - - rs110391 14:88385741 G - - - intergenic_variant - - - - - - rs2165571 14:88538048 G 283587 NR_046094.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2165571 14:88538048 G ENSESTG00000034028 ENSESTT00000086014 Transcript intron_variant - - - - - - rs1742136 14:88688315 C CCDS9880.1 CCDS9880.1 Transcript intron_variant - - - - - - rs1742136 14:88688315 C 54207 NM_021161.4 Transcript intron_variant - - - - - - rs1742136 14:88688315 C CCDS9882.1 CCDS9882.1 Transcript intron_variant - - - - - - rs1742136 14:88688315 C 54207 NM_138318.2 Transcript intron_variant - - - - - - rs1742136 14:88688315 C CCDS9881.1 CCDS9881.1 Transcript intron_variant - - - - - - rs1742136 14:88688315 C 54207 NM_138317.2 Transcript intron_variant - - - - - - rs414300 14:88737654 A CCDS9882.1 CCDS9882.1 Transcript upstream_gene_variant - - - - - - DISTANCE=521 rs414300 14:88737654 A 54207 NM_138318.2 Transcript upstream_gene_variant - - - - - - DISTANCE=399 rs414300 14:88737654 A CCDS9881.1 CCDS9881.1 Transcript intron_variant - - - - - - rs414300 14:88737654 A 54207 NM_021161.4 Transcript intron_variant - - - - - - rs414300 14:88737654 A CCDS9880.1 CCDS9880.1 Transcript intron_variant - - - - - - rs414300 14:88737654 A ENSESTG00000034221 ENSESTT00000086529 Transcript intron_variant - - - - - - rs414300 14:88737654 A 54207 NM_138317.2 Transcript intron_variant - - - - - - rs414300 14:88737654 A ENSESTG00000034221 ENSESTT00000086535 Transcript intron_variant - - - - - - rs414300 14:88737654 A ENSESTG00000034221 ENSESTT00000086527 Transcript intron_variant - - - - - - rs386579 14:88895669 G 55812 NM_018418.4 Transcript intron_variant - - - - - - rs386579 14:88895669 G ENSESTG00000034041 ENSESTT00000086075 Transcript intron_variant - - - - - - rs386579 14:88895669 G ENSESTG00000034041 ENSESTT00000086096 Transcript upstream_gene_variant - - - - - - DISTANCE=1846 rs386579 14:88895669 G ENSESTG00000034041 ENSESTT00000086068 Transcript intron_variant - - - - - - rs386579 14:88895669 G 55812 NM_001040428.3 Transcript intron_variant - - - - - - rs386579 14:88895669 G CCDS9883.1 CCDS9883.1 Transcript intron_variant - - - - - - rs386579 14:88895669 G ENSESTG00000034041 ENSESTT00000086094 Transcript upstream_gene_variant - - - - - - DISTANCE=22 rs386579 14:88895669 G ENSESTG00000034041 ENSESTT00000086082 Transcript intron_variant - - - - - - rs386579 14:88895669 G CCDS32132.1 CCDS32132.1 Transcript intron_variant - - - - - - rs386579 14:88895669 G ENSESTG00000034041 ENSESTT00000086084 Transcript intron_variant - - - - - - rs845764 14:88905812 G 55812 NM_018418.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1008 rs845764 14:88905812 G ENSESTG00000034041 ENSESTT00000086075 Transcript downstream_gene_variant - - - - - - DISTANCE=1010 rs845764 14:88905812 G ENSESTG00000034041 ENSESTT00000086096 Transcript intron_variant - - - - - - rs845764 14:88905812 G ENSESTG00000034041 ENSESTT00000086068 Transcript intron_variant - - - - - - rs845764 14:88905812 G 55812 NM_001040428.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1008 rs845764 14:88905812 G CCDS9883.1 CCDS9883.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1046 rs845764 14:88905812 G ENSESTG00000034041 ENSESTT00000086094 Transcript intron_variant - - - - - - rs845764 14:88905812 G ENSESTG00000034041 ENSESTT00000086082 Transcript intron_variant - - - - - - rs845764 14:88905812 G CCDS32132.1 CCDS32132.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1046 rs845764 14:88905812 G ENSESTG00000034041 ENSESTT00000086084 Transcript downstream_gene_variant - - - - - - DISTANCE=1010 rs2772515 14:88944060 T ENSESTG00000034209 ENSESTT00000086495 Transcript downstream_gene_variant - - - - - - DISTANCE=2382 rs2772515 14:88944060 T ENSESTG00000034218 ENSESTT00000086507 Transcript intron_variant - - - - - - rs2772515 14:88944060 T 11099 NM_007039.3 Transcript intron_variant - - - - - - rs2772515 14:88944060 T CCDS9884.1 CCDS9884.1 Transcript intron_variant - - - - - - rs6575014 14:89062671 G CCDS32134.1 CCDS32134.1 Transcript intron_variant - - - - - - rs6575014 14:89062671 G ENSESTG00000034078 ENSESTT00000086261 Transcript intron_variant - - - - - - rs6575014 14:89062671 G 79882 NM_207660.3 Transcript intron_variant - - - - - - rs6575014 14:89062671 G CCDS32135.1 CCDS32135.1 Transcript intron_variant - - - - - - rs6575014 14:89062671 G 79882 NM_001160103.1 Transcript intron_variant - - - - - - rs6575014 14:89062671 G 79882 NM_207661.2 Transcript intron_variant - - - - - - rs6575014 14:89062671 G 79882 NM_207662.3 Transcript intron_variant - - - - - - rs6575014 14:89062671 G CCDS32133.1 CCDS32133.1 Transcript intron_variant - - - - - - rs6575014 14:89062671 G ENSESTG00000034078 ENSESTT00000086263 Transcript intron_variant - - - - - - rs6575014 14:89062671 G ENSESTG00000034078 ENSESTT00000086253 Transcript intron_variant - - - - - - rs6575014 14:89062671 G ENSESTG00000034078 ENSESTT00000086227 Transcript intron_variant - - - - - - rs6575014 14:89062671 G ENSESTG00000034078 ENSESTT00000086240 Transcript intron_variant - - - - - - rs6575014 14:89062671 G 79882 NM_001160104.1 Transcript intron_variant - - - - - - rs6575014 14:89062671 G 79882 NM_024824.4 Transcript intron_variant - - - - - - rs6575014 14:89062671 G ENSESTG00000034078 ENSESTT00000086257 Transcript intron_variant - - - - - - rs6575014 14:89062671 G ENSESTG00000034078 ENSESTT00000086220 Transcript intron_variant - - - - - - rs6575014 14:89062671 G CCDS55938.1 CCDS55938.1 Transcript intron_variant - - - - - - rs6575014 14:89062671 G ENSESTG00000034078 ENSESTT00000086255 Transcript intron_variant - - - - - - rs6575014 14:89062671 G CCDS32136.1 CCDS32136.1 Transcript intron_variant - - - - - - rs6575014 14:89062671 G ENSESTG00000034078 ENSESTT00000086262 Transcript intron_variant - - - - - - rs6575015 14:89062739 G CCDS32134.1 CCDS32134.1 Transcript intron_variant - - - - - - rs6575015 14:89062739 G ENSESTG00000034078 ENSESTT00000086261 Transcript intron_variant - - - - - - rs6575015 14:89062739 G 79882 NM_207660.3 Transcript intron_variant - - - - - - rs6575015 14:89062739 G CCDS32135.1 CCDS32135.1 Transcript intron_variant - - - - - - rs6575015 14:89062739 G 79882 NM_001160103.1 Transcript intron_variant - - - - - - rs6575015 14:89062739 G 79882 NM_207661.2 Transcript intron_variant - - - - - - rs6575015 14:89062739 G 79882 NM_207662.3 Transcript intron_variant - - - - - - rs6575015 14:89062739 G CCDS32133.1 CCDS32133.1 Transcript intron_variant - - - - - - rs6575015 14:89062739 G ENSESTG00000034078 ENSESTT00000086263 Transcript intron_variant - - - - - - rs6575015 14:89062739 G ENSESTG00000034078 ENSESTT00000086253 Transcript intron_variant - - - - - - rs6575015 14:89062739 G ENSESTG00000034078 ENSESTT00000086227 Transcript intron_variant - - - - - - rs6575015 14:89062739 G ENSESTG00000034078 ENSESTT00000086240 Transcript intron_variant - - - - - - rs6575015 14:89062739 G 79882 NM_001160104.1 Transcript intron_variant - - - - - - rs6575015 14:89062739 G 79882 NM_024824.4 Transcript intron_variant - - - - - - rs6575015 14:89062739 G ENSESTG00000034078 ENSESTT00000086257 Transcript intron_variant - - - - - - rs6575015 14:89062739 G ENSESTG00000034078 ENSESTT00000086220 Transcript intron_variant - - - - - - rs6575015 14:89062739 G CCDS55938.1 CCDS55938.1 Transcript intron_variant - - - - - - rs6575015 14:89062739 G ENSESTG00000034078 ENSESTT00000086255 Transcript intron_variant - - - - - - rs6575015 14:89062739 G CCDS32136.1 CCDS32136.1 Transcript intron_variant - - - - - - rs6575015 14:89062739 G ENSESTG00000034078 ENSESTT00000086262 Transcript intron_variant - - - - - - rs2761400 14:89576523 A - - - intergenic_variant - - - - - - rs1287608 14:89599138 C ENSESTG00000004121 ENSESTT00000010428 Transcript intron_variant - - - - - - rs6575041 14:89649688 A CCDS32138.1 CCDS32138.1 Transcript intron_variant - - - - - - rs6575041 14:89649688 A ENSESTG00000004121 ENSESTT00000010408 Transcript intron_variant - - - - - - rs6575041 14:89649688 A CCDS41977.1 CCDS41977.1 Transcript intron_variant - - - - - - rs6575041 14:89649688 A ENSESTG00000004121 ENSESTT00000010428 Transcript upstream_gene_variant - - - - - - DISTANCE=2600 rs6575041 14:89649688 A ENSESTG00000004121 ENSESTT00000010417 Transcript intron_variant - - - - - - rs6575041 14:89649688 A 1112 NM_005197.3 Transcript intron_variant - - - - - - rs6575041 14:89649688 A ENSESTG00000004121 ENSESTT00000010400 Transcript intron_variant - - - - - - rs6575041 14:89649688 A 1112 NM_001085471.1 Transcript intron_variant - - - - - - rs6575041 14:89649688 A ENSESTG00000004121 ENSESTT00000010421 Transcript intron_variant - - - - - - rs8009157 14:89659750 A CCDS32138.1 CCDS32138.1 Transcript intron_variant - - - - - - rs8009157 14:89659750 A ENSESTG00000004121 ENSESTT00000010408 Transcript intron_variant - - - - - - rs8009157 14:89659750 A CCDS41977.1 CCDS41977.1 Transcript intron_variant - - - - - - rs8009157 14:89659750 A ENSESTG00000004121 ENSESTT00000010417 Transcript intron_variant - - - - - - rs8009157 14:89659750 A 1112 NM_005197.3 Transcript intron_variant - - - - - - rs8009157 14:89659750 A ENSESTG00000004121 ENSESTT00000010400 Transcript intron_variant - - - - - - rs8009157 14:89659750 A 1112 NM_001085471.1 Transcript intron_variant - - - - - - rs8009157 14:89659750 A ENSESTG00000004121 ENSESTT00000010421 Transcript upstream_gene_variant - - - - - - DISTANCE=2955 rs1152389 14:89913249 C 1112 NM_001085471.1 Transcript intron_variant - - - - - - rs1286929 14:90435913 A CCDS9888.1 CCDS9888.1 Transcript intron_variant - - - - - - rs1286929 14:90435913 A ENSESTG00000004063 ENSESTT00000010321 Transcript intron_variant - - - - - - rs1286929 14:90435913 A ENSESTG00000004063 ENSESTT00000010317 Transcript intron_variant - - - - - - rs1286929 14:90435913 A ENSESTG00000004063 ENSESTT00000010316 Transcript intron_variant - - - - - - rs1286929 14:90435913 A ENSESTG00000004063 ENSESTT00000010297 Transcript intron_variant - - - - - - rs1286929 14:90435913 A 55775 NM_018319.3 Transcript intron_variant - - - - - - rs1286929 14:90435913 A ENSESTG00000004063 ENSESTT00000010323 Transcript intron_variant - - - - - - rs1286929 14:90435913 A 55775 NM_001008744.1 Transcript intron_variant - - - - - - rs1286929 14:90435913 A ENSESTG00000004063 ENSESTT00000010305 Transcript intron_variant - - - - - - rs6575119 14:90723109 G - ENSR00000422398 RegulatoryFeature regulatory_region_variant - - - - - - rs6575119 14:90723109 G ENSESTG00000015002 ENSESTT00000037735 Transcript upstream_gene_variant - - - - - - DISTANCE=2394 rs6575119 14:90723109 G CCDS32139.1 CCDS32139.1 Transcript intron_variant - - - - - - rs6575119 14:90723109 G ENSESTG00000015002 ENSESTT00000037622 Transcript intron_variant - - - - - - rs6575119 14:90723109 G 5700 NM_002802.2 Transcript intron_variant - - - - - - rs8006293 14:90878680 G - ENSR00001459605 RegulatoryFeature regulatory_region_variant - - - - - - rs8006293 14:90878680 G 801 NM_006888.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4061 rs1294579 14:91016530 A - ENSR00000099384 RegulatoryFeature regulatory_region_variant - - - - - - rs1294579 14:91016530 A ENSESTG00000015265 ENSESTT00000038316 Transcript intron_variant - - - - - - rs1294579 14:91016530 A 145567 NM_001010854.1 Transcript intron_variant - - - - - - rs1294579 14:91016530 A CCDS32140.1 CCDS32140.1 Transcript intron_variant - - - - - - rs1294579 14:91016530 A ENSESTG00000015265 ENSESTT00000038321 Transcript intron_variant - - - - - - rs1294579 14:91016530 A ENSESTG00000015265 ENSESTT00000038343 Transcript intron_variant - - - - - - rs1294579 14:91016530 A ENSESTG00000015265 ENSESTT00000038326 Transcript intron_variant - - - - - - rs1294579 14:91016530 A ENSESTG00000015265 ENSESTT00000038285 Transcript intron_variant - - - - - - rs1286299 14:91297565 G - - - intergenic_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002074 Transcript intron_variant - - - - - - rs8003030 14:91679962 A 80017 NM_001102369.1 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002089 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002124 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002090 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002125 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002121 Transcript intron_variant - - - - - - rs8003030 14:91679962 A CCDS41979.1 CCDS41979.1 Transcript intron_variant - - - - - - rs8003030 14:91679962 A 80017 NM_024952.6 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002109 Transcript intron_variant - - - - - - rs8003030 14:91679962 A 80017 NM_001102367.1 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002118 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002097 Transcript intron_variant - - - - - - rs8003030 14:91679962 A 80017 NM_001102368.1 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002134 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002127 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002098 Transcript intron_variant - - - - - - rs8003030 14:91679962 A CCDS32141.1 CCDS32141.1 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002135 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002069 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002108 Transcript intron_variant - - - - - - rs8003030 14:91679962 A CCDS45150.1 CCDS45150.1 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002093 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002076 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002119 Transcript intron_variant - - - - - - rs8003030 14:91679962 A 80017 NM_001102366.1 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002096 Transcript intron_variant - - - - - - rs8003030 14:91679962 A ENSESTG00000000843 ENSESTT00000002112 Transcript intron_variant - - - - - - rs2758136 14:91704124 C ENSESTG00000001037 ENSESTT00000002481 Transcript intron_variant - - - - - - rs2758136 14:91704124 C ENSESTG00000001037 ENSESTT00000002476 Transcript intron_variant - - - - - - rs2758136 14:91704124 C 8111 NM_003485.3 Transcript intron_variant - - - - - - rs2758136 14:91704124 C CCDS9894.2 CCDS9894.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2730 rs2758136 14:91704124 C 8111 NM_001177676.1 Transcript intron_variant - - - - - - rs1285764 14:91772522 T - ENSR00000422571 RegulatoryFeature regulatory_region_variant - - - - - - rs1285764 14:91772522 T CCDS45151.1 CCDS45151.1 Transcript intron_variant - - - - - - rs1285764 14:91772522 T 440193 NM_001080414.3 Transcript intron_variant - - - - - - rs1285765 14:91775933 G CCDS45151.1 CCDS45151.1 Transcript intron_variant - - - - - - rs1285765 14:91775933 G ENSESTG00000001022 ENSESTT00000002463 Transcript downstream_gene_variant - - - - - - DISTANCE=4408 rs1285765 14:91775933 G 440193 NM_001080414.3 Transcript intron_variant - - - - - - rs1285822 14:91845290 G CCDS45151.1 CCDS45151.1 Transcript intron_variant - - - - - - rs1285822 14:91845290 G ENSESTG00000001002 ENSESTT00000002423 Transcript downstream_gene_variant - - - - - - DISTANCE=545 rs1285822 14:91845290 G 440193 NM_001080414.3 Transcript intron_variant - - - - - - rs1704613 14:92041890 G - - - intergenic_variant - - - - - - rs8022792 14:92254576 A 123036 NM_001128596.1 Transcript intron_variant - - - - - - rs8022792 14:92254576 A 123036 NM_001128595.1 Transcript intron_variant - - - - - - rs8022792 14:92254576 A 123036 NM_152332.4 Transcript intron_variant - - - - - - rs8022792 14:92254576 A ENSESTG00000000969 ENSESTT00000002330 Transcript intron_variant - - - - - - rs8022792 14:92254576 A ENSESTG00000000969 ENSESTT00000002326 Transcript intron_variant - - - - - - rs8022792 14:92254576 A CCDS9897.1 CCDS9897.1 Transcript intron_variant - - - - - - rs2430352 14:92354801 A ENSESTG00000000914 ENSESTT00000002273 Transcript intron_variant - - - - - - rs2430352 14:92354801 A CCDS9898.1 CCDS9898.1 Transcript intron_variant - - - - - - rs2430352 14:92354801 A ENSESTG00000000914 ENSESTT00000002267 Transcript intron_variant - - - - - - rs2430352 14:92354801 A 10516 NM_006329.3 Transcript intron_variant - - - - - - rs1241709 14:92666454 G - - - intergenic_variant - - - - - - rs10873417 14:92693039 C - - - intergenic_variant - - - - - - rs7143549 14:92823048 C ENSESTG00000003097 ENSESTT00000007697 Transcript intron_variant - - - - - - rs7143549 14:92823048 C 123041 NM_153647.3 Transcript intron_variant - - - - - - rs7143549 14:92823048 C 123041 NM_153646.3 Transcript intron_variant - - - - - - rs7143549 14:92823048 C 123041 NM_153648.3 Transcript intron_variant - - - - - - rs7143549 14:92823048 C CCDS45156.1 CCDS45156.1 Transcript intron_variant - - - - - - rs7143549 14:92823048 C CCDS9903.2 CCDS9903.2 Transcript intron_variant - - - - - - rs7143549 14:92823048 C CCDS45155.2 CCDS45155.2 Transcript intron_variant - - - - - - rs6575271 14:93110986 T - ENSR00000422740 RegulatoryFeature regulatory_region_variant - - - - - - rs6575271 14:93110986 T CCDS32144.1 CCDS32144.1 Transcript intron_variant - - - - - - rs6575271 14:93110986 T 79890 NM_024832.3 Transcript intron_variant - - - - - - rs6575271 14:93110986 T ENSESTG00000003122 ENSESTT00000007761 Transcript intron_variant - - - - - - rs6575271 14:93110986 T ENSESTG00000003122 ENSESTT00000007766 Transcript 5_prime_UTR_variant 311 - - - - - rs1885755 14:93132344 G - ENSR00000241600 RegulatoryFeature regulatory_region_variant - - - - - - rs1885755 14:93132344 G CCDS32144.1 CCDS32144.1 Transcript intron_variant - - - - - - rs1885755 14:93132344 G 79890 NM_024832.3 Transcript intron_variant - - - - - - rs1885755 14:93132344 G ENSESTG00000003134 ENSESTT00000007787 Transcript intron_variant - - - - - - rs2402216 14:93372078 C - - - intergenic_variant - - - - - - rs943321 14:94105429 G 57578 NM_020818.3 Transcript intron_variant - - - - - - rs943321 14:94105429 G CCDS9911.2 CCDS9911.2 Transcript intron_variant - - - - - - rs8006438 14:94198401 A 145270 NM_178013.3 Transcript intron_variant - - - - - - rs8006438 14:94198401 A CCDS9912.1 CCDS9912.1 Transcript intron_variant - - - - - - rs8006438 14:94198401 A ENSESTG00000034283 ENSESTT00000086680 Transcript intron_variant - - - - - - rs7158850 14:94250430 G 145270 NM_178013.3 Transcript intron_variant - - - - - - rs7158850 14:94250430 G CCDS9912.1 CCDS9912.1 Transcript intron_variant - - - - - - rs7158850 14:94250430 G ENSESTG00000034283 ENSESTT00000086680 Transcript intron_variant - - - - - - rs4900221 14:94606731 G - - - intergenic_variant - - - - - - rs1884551 14:94797559 C - ENSR00001459892 RegulatoryFeature regulatory_region_variant - - - - - - rs1884551 14:94797559 C - - - intergenic_variant - - - - - - rs1950655 14:94805304 C - - - intergenic_variant - - - - - - rs2736900 14:94822812 T - - - intergenic_variant - - - - - - rs4905201 14:94896600 C - - - intergenic_variant - - - - - - rs59407226 14:94985735 G 145264 NM_173850.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1554 rs1243556 14:95364904 C - - - intergenic_variant - - - - - - rs4509950 14:95520507 A ENSESTG00000010556 ENSESTT00000026410 Transcript downstream_gene_variant - - - - - - DISTANCE=3218 rs58086956 14:95759225 C ENSESTG00000010621 ENSESTT00000026602 Transcript intron_variant - - - - - - rs58086956 14:95759225 C 79789 NM_024734.3 Transcript intron_variant - - - - - - rs58086956 14:95759225 C ENSESTG00000010621 ENSESTT00000026598 Transcript intron_variant - - - - - - rs58086956 14:95759225 C ENSESTG00000010621 ENSESTT00000026594 Transcript intron_variant - - - - - - rs58086956 14:95759225 C CCDS9933.1 CCDS9933.1 Transcript intron_variant - - - - - - rs1187746 14:95944557 T 161176 NM_152592.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2384 rs1187746 14:95944557 T CCDS9935.1 CCDS9935.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2399 rs1187746 14:95944557 T ENSESTG00000010610 ENSESTT00000026543 Transcript upstream_gene_variant - - - - - - DISTANCE=2519 rs1748955 14:96153210 C ENSESTG00000010592 ENSESTT00000026502 Transcript intron_variant - - - - - - rs1748955 14:96153210 C 9623 NM_004918.3 Transcript intron_variant - - - - - - rs1748955 14:96153210 C CCDS32151.1 CCDS32151.1 Transcript intron_variant - - - - - - rs1957938 14:96184690 T CCDS9941.1 CCDS9941.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4287 rs1957938 14:96184690 T 8115 NM_021966.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4157 rs1957938 14:96184690 T 8115 NR_049726.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4157 rs1957938 14:96184690 T ENSESTG00000010602 ENSESTT00000026537 Transcript upstream_gene_variant - - - - - - DISTANCE=4238 rs1957938 14:96184690 T 8115 NM_001098725.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4157 rs6575555 14:96413432 C - ENSR00000423236 RegulatoryFeature regulatory_region_variant - - - - - - rs6575555 14:96413432 C - - - intergenic_variant - - - - - - rs4905531 14:97202357 C - - - intergenic_variant - - - - - - rs7158810 14:97651260 G - - - intergenic_variant - - - - - - rs1958846 14:97816036 A - - - intergenic_variant - - - - - - rs1462252 14:98200845 A - - - intergenic_variant - - - - - - rs28592813 14:98308724 A - - - intergenic_variant - - - - - - rs2604980 14:98312606 G - - - intergenic_variant - - - - - - rs2607046 14:98392383 A 388011 NR_015430.1 Transcript non_coding_exon_variant,nc_transcript_variant 1022 - - - - - rs2607046 14:98392383 A ENSESTG00000023577 ENSESTT00000059419 Transcript downstream_gene_variant - - - - - - DISTANCE=306 rs1478063 14:98465252 T - - - intergenic_variant - - - - - - rs857069 14:98502567 G - - - intergenic_variant - - - - - - rs2150503 14:98799623 A - - - intergenic_variant - - - - - - rs4905679 14:98814761 G - - - intergenic_variant - - - - - - rs4905681 14:98815390 T - - - intergenic_variant - - - - - - rs930923 14:98818914 G - - - intergenic_variant - - - - - - rs1958811 14:98831520 C - - - intergenic_variant - - - - - - rs10146322 14:98836412 A - - - intergenic_variant - - - - - - rs1380213 14:98924174 G - - - intergenic_variant - - - - - - rs6420934 14:98931145 T - - - intergenic_variant - - - - - - rs1952873 14:98939053 G - - - intergenic_variant - - - - - - rs1951101 14:98966607 G ENSESTG00000001659 ENSESTT00000004008 Transcript intron_variant - - - - - - rs1475017 14:99026848 G - - - intergenic_variant - - - - - - rs10129474 14:99132659 G - - - intergenic_variant - - - - - - rs7143509 14:99358154 G - - - intergenic_variant - - - - - - rs2638837 14:99512667 C - - - intergenic_variant - - - - - - rs2933339 14:99523570 C - - - intergenic_variant - - - - - - rs2748803 14:99762921 G - ENSR00000652689 RegulatoryFeature regulatory_region_variant - - - - - - rs2748803 14:99762921 G - - - intergenic_variant - - - - - - rs2664302 14:99771714 A - - - intergenic_variant - - - - - - rs1257317 14:99806608 G - - - intergenic_variant - - - - - - rs2614466 14:99815416 A - - - intergenic_variant - - - - - - rs2614455 14:99851007 G - - - intergenic_variant - - - - - - rs2181229 14:100172480 A 10858 NM_006668.1 Transcript intron_variant - - - - - - rs2181229 14:100172480 A ENSESTG00000010323 ENSESTT00000025827 Transcript intron_variant - - - - - - rs2181229 14:100172480 A ENSESTG00000010323 ENSESTT00000025833 Transcript intron_variant - - - - - - rs2181229 14:100172480 A CCDS9954.1 CCDS9954.1 Transcript intron_variant - - - - - - rs2181229 14:100172480 A ENSESTG00000010323 ENSESTT00000025836 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025950 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025946 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025987 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025982 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025976 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025986 Transcript intron_variant - - - - - - rs10151491 14:100263406 C CCDS32155.1 CCDS32155.1 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025989 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025959 Transcript intron_variant - - - - - - rs10151491 14:100263406 C 2009 NM_004434.2 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025983 Transcript intron_variant - - - - - - rs10151491 14:100263406 C CCDS32154.1 CCDS32154.1 Transcript intron_variant - - - - - - rs10151491 14:100263406 C 2009 NM_001008707.1 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025962 Transcript intron_variant - - - - - - rs10151491 14:100263406 C ENSESTG00000010354 ENSESTT00000025977 Transcript intron_variant - - - - - - rs4905921 14:100411038 T ENSESTG00000010354 ENSESTT00000025946 Transcript downstream_gene_variant - - - - - - DISTANCE=4585 rs4905921 14:100411038 T ENSESTG00000010354 ENSESTT00000025976 Transcript downstream_gene_variant - - - - - - DISTANCE=4585 rs4905921 14:100411038 T ENSESTG00000034102 ENSESTT00000086196 Transcript downstream_gene_variant - - - - - - DISTANCE=4536 rs4905921 14:100411038 T ENSESTG00000010354 ENSESTT00000025999 Transcript downstream_gene_variant - - - - - - DISTANCE=4585 rs4905921 14:100411038 T CCDS32155.1 CCDS32155.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4589 rs4905921 14:100411038 T 2009 NM_004434.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2641 rs4905921 14:100411038 T CCDS32154.1 CCDS32154.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4589 rs4905921 14:100411038 T ENSESTG00000010354 ENSESTT00000025992 Transcript downstream_gene_variant - - - - - - DISTANCE=4585 rs4905921 14:100411038 T 2009 NM_001008707.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2641 rs4905921 14:100411038 T ENSESTG00000034102 ENSESTT00000086198 Transcript downstream_gene_variant - - - - - - DISTANCE=4527 rs4905921 14:100411038 T ENSESTG00000010354 ENSESTT00000025977 Transcript downstream_gene_variant - - - - - - DISTANCE=4585 rs4905929 14:100503983 A - ENSR00000423694 RegulatoryFeature regulatory_region_variant - - - - - - rs4905929 14:100503983 A ENSESTG00000034122 ENSESTT00000086246 Transcript intron_variant - - - - - - rs1190970 14:100541201 G ENSESTG00000034122 ENSESTT00000086329 Transcript intron_variant - - - - - - rs1190970 14:100541201 G ENSESTG00000034122 ENSESTT00000086319 Transcript intron_variant - - - - - - rs1190970 14:100541201 G ENSESTG00000034122 ENSESTT00000086246 Transcript intron_variant - - - - - - rs1190970 14:100541201 G ENSESTG00000034122 ENSESTT00000086325 Transcript intron_variant - - - - - - rs1190970 14:100541201 G 51466 NM_016337.2 Transcript intron_variant - - - - - - rs1190970 14:100541201 G ENSESTG00000034122 ENSESTT00000086330 Transcript intron_variant - - - - - - rs1190970 14:100541201 G CCDS9955.1 CCDS9955.1 Transcript intron_variant - - - - - - rs1190970 14:100541201 G ENSESTG00000034122 ENSESTT00000086315 Transcript intron_variant - - - - - - rs1190973 14:100546917 G ENSESTG00000034122 ENSESTT00000086329 Transcript intron_variant - - - - - - rs1190973 14:100546917 G ENSESTG00000034122 ENSESTT00000086319 Transcript intron_variant - - - - - - rs1190973 14:100546917 G ENSESTG00000034122 ENSESTT00000086246 Transcript intron_variant - - - - - - rs1190973 14:100546917 G ENSESTG00000034122 ENSESTT00000086325 Transcript intron_variant - - - - - - rs1190973 14:100546917 G 51466 NM_016337.2 Transcript intron_variant - - - - - - rs1190973 14:100546917 G ENSESTG00000034122 ENSESTT00000086330 Transcript intron_variant - - - - - - rs1190973 14:100546917 G CCDS9955.1 CCDS9955.1 Transcript intron_variant - - - - - - rs1190973 14:100546917 G ENSESTG00000034122 ENSESTT00000086315 Transcript intron_variant - - - - - - rs3118496 14:100696991 C - - - intergenic_variant - - - - - - rs10147112 14:100737445 G CCDS9957.1 CCDS9957.1 Transcript intron_variant - - - - - - rs10147112 14:100737445 G ENSESTG00000034166 ENSESTT00000086407 Transcript intron_variant - - - - - - rs10147112 14:100737445 G 7528 NM_003403.3 Transcript intron_variant - - - - - - rs7140648 14:101044977 G - - - intergenic_variant - - - - - - rs6575811 14:101517425 G 664616 NR_030267.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4550 rs6575811 14:101517425 G 619555 NR_030162.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1358 rs6575811 14:101517425 G 574436 NR_030160.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4331 rs6575811 14:101517425 G 494331 NR_029874.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3218 rs6575811 14:101517425 G 664612 NR_030256.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3690 rs6575811 14:101517425 G 100126345 NR_030595.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3109 rs6575811 14:101517425 G 664613 NR_030257.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2340 rs6575811 14:101517425 G 768214 NR_030408.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4170 rs6575811 14:101517425 G 406924 NR_029698.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3599 rs6575811 14:101517425 G 724025 NR_030391.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1442 rs7155784 14:101947083 G - ENSR00000652728 RegulatoryFeature regulatory_region_variant - - - - - - rs7155784 14:101947083 G - - - intergenic_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054822 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054611 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054888 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054692 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054918 Transcript upstream_gene_variant - - - - - - DISTANCE=2904 rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054862 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054621 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054779 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054893 Transcript intron_variant - - - - - - rs2476519 14:102287086 T CCDS53911.1 CCDS53911.1 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054928 Transcript upstream_gene_variant - - - - - - DISTANCE=2968 rs2476519 14:102287086 T CCDS9965.1 CCDS9965.1 Transcript intron_variant - - - - - - rs2476519 14:102287086 T 5527 NM_002719.3 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054813 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054757 Transcript intron_variant - - - - - - rs2476519 14:102287086 T 5527 NM_178587.2 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054783 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054576 Transcript intron_variant - - - - - - rs2476519 14:102287086 T 5527 NM_178586.2 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054837 Transcript intron_variant - - - - - - rs2476519 14:102287086 T CCDS53912.1 CCDS53912.1 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054680 Transcript intron_variant - - - - - - rs2476519 14:102287086 T 5527 NM_001161726.1 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054736 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054744 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054781 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054823 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054738 Transcript intron_variant - - - - - - rs2476519 14:102287086 T ENSESTG00000021647 ENSESTT00000054884 Transcript intron_variant - - - - - - rs2476519 14:102287086 T 5527 NM_001161725.1 Transcript intron_variant - - - - - - rs2476519 14:102287086 T CCDS9964.1 CCDS9964.1 Transcript intron_variant - - - - - - rs2476519 14:102287086 T CCDS45163.1 CCDS45163.1 Transcript intron_variant - - - - - - rs1190559 14:102684388 C ENSESTG00000035557 ENSESTT00000089817 Transcript intron_variant - - - - - - rs1190559 14:102684388 C ENSESTG00000035557 ENSESTT00000089809 Transcript intron_variant - - - - - - rs1190559 14:102684388 C 91833 NM_181291.2 Transcript intron_variant - - - - - - rs1190559 14:102684388 C CCDS9968.1 CCDS9968.1 Transcript intron_variant - - - - - - rs1190559 14:102684388 C ENSESTG00000035584 ENSESTT00000089886 Transcript intron_variant - - - - - - rs1190559 14:102684388 C CCDS55945.1 CCDS55945.1 Transcript intron_variant - - - - - - rs1190559 14:102684388 C 91833 NM_001242415.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3046 rs1190559 14:102684388 C 91833 NM_001242416.1 Transcript intron_variant - - - - - - rs1190559 14:102684388 C ENSESTG00000035557 ENSESTT00000089816 Transcript intron_variant - - - - - - rs6575913 14:102872261 C CCDS58337.1 CCDS58337.1 Transcript intron_variant - - - - - - rs6575913 14:102872261 C ENSESTG00000035562 ENSESTT00000089834 Transcript intron_variant - - - - - - rs6575913 14:102872261 C 9895 NM_014844.3 Transcript intron_variant - - - - - - rs6575913 14:102872261 C 9895 NM_001172631.1 Transcript intron_variant - - - - - - rs6575913 14:102872261 C ENSESTG00000035562 ENSESTT00000089833 Transcript intron_variant - - - - - - rs6575913 14:102872261 C CCDS32162.1 CCDS32162.1 Transcript intron_variant - - - - - - rs10137161 14:103934488 C 4140 NM_001128921.1 Transcript missense_variant 1658 992 331 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs10137161 14:103934488 C ENSESTG00000015352 ENSESTT00000038570 Transcript missense_variant 1328 1193 398 F/S tTt/tCt - rs10137161 14:103934488 C CCDS55947.1 CCDS55947.1 Transcript missense_variant 1181 1181 394 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs10137161 14:103934488 C ENSESTG00000015352 ENSESTT00000038580 Transcript missense_variant 1280 1145 382 F/S tTt/tCt - rs10137161 14:103934488 C 4140 NM_001128919.1 Transcript missense_variant 1895 1229 410 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs10137161 14:103934488 C ENSESTG00000015352 ENSESTT00000038589 Transcript missense_variant 1065 893 298 F/S tTt/tCt - rs10137161 14:103934488 C CCDS45166.1 CCDS45166.1 Transcript missense_variant 1229 1229 410 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs10137161 14:103934488 C 4140 NM_002376.5 Transcript missense_variant 1895 1229 410 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs10137161 14:103934488 C CCDS41993.1 CCDS41993.1 Transcript missense_variant 1229 1229 410 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs10137161 14:103934488 C ENSESTG00000015352 ENSESTT00000038587 Transcript missense_variant 1113 941 314 F/S tTt/tCt - rs10137161 14:103934488 C 4140 NM_001128918.1 Transcript missense_variant 1895 1229 410 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs10137161 14:103934488 C CCDS45167.1 CCDS45167.1 Transcript missense_variant 992 992 331 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs10137161 14:103934488 C CCDS45165.1 CCDS45165.1 Transcript missense_variant 1229 1229 410 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs10137161 14:103934488 C 4140 NM_001128920.1 Transcript missense_variant 1847 1181 394 F/S tTt/tCt - PolyPhen=benign;SIFT=tolerated rs12050258 14:104297981 T CCDS41997.1 CCDS41997.1 Transcript intron_variant - - - - - - rs12050258 14:104297981 T ENSESTG00000015662 ENSESTT00000039244 Transcript intron_variant - - - - - - rs12050258 14:104297981 T ENSESTG00000015662 ENSESTT00000039260 Transcript intron_variant - - - - - - rs12050258 14:104297981 T 23368 NM_015316.2 Transcript intron_variant - - - - - - rs3117717 14:104543817 A - - - intergenic_variant - - - - - - rs946997 14:104650117 C CCDS45171.1 CCDS45171.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3990 rs946997 14:104650117 C 26153 NM_015656.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2882 rs946997 14:104650117 C ENSESTG00000026750 ENSESTT00000067387 Transcript downstream_gene_variant - - - - - - DISTANCE=2940 rs28453989 14:104940930 T ENSESTG00000027379 ENSESTT00000068951 Transcript downstream_gene_variant - - - - - - DISTANCE=85 rs4357866 14:105049661 A ENSESTG00000026789 ENSESTT00000067493 Transcript intron_variant - - - - - - rs4357866 14:105049661 A 400258 NM_001008404.1 Transcript intron_variant - - - - - - rs4357866 14:105049661 A ENSESTG00000026789 ENSESTT00000067515 Transcript intron_variant - - - - - - rs4357866 14:105049661 A ENSESTG00000027379 ENSESTT00000068951 Transcript intron_variant - - - - - - rs4357866 14:105049661 A CCDS32166.1 CCDS32166.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3107 rs4357866 14:105049661 A ENSESTG00000026789 ENSESTT00000067499 Transcript intron_variant - - - - - - rs2498798 14:105240530 C ENSESTG00000027194 ENSESTT00000068858 Transcript intron_variant - - - - - - rs2498798 14:105240530 C ENSESTG00000027194 ENSESTT00000068790 Transcript intron_variant - - - - - - rs2498798 14:105240530 C ENSESTG00000027194 ENSESTT00000068823 Transcript intron_variant - - - - - - rs2498798 14:105240530 C ENSESTG00000027194 ENSESTT00000068840 Transcript intron_variant - - - - - - rs2498798 14:105240530 C ENSESTG00000027194 ENSESTT00000068902 Transcript intron_variant - - - - - - rs2498798 14:105240530 C ENSESTG00000027194 ENSESTT00000068887 Transcript intron_variant - - - - - - rs2498798 14:105240530 C 207 NM_001014431.1 Transcript intron_variant - - - - - - rs2498798 14:105240530 C CCDS9994.1 CCDS9994.1 Transcript intron_variant - - - - - - rs2498798 14:105240530 C ENSESTG00000027194 ENSESTT00000068897 Transcript intron_variant - - - - - - rs2498798 14:105240530 C 207 NM_005163.2 Transcript intron_variant - - - - - - rs2498798 14:105240530 C ENSESTG00000027194 ENSESTT00000068905 Transcript intron_variant - - - - - - rs2498798 14:105240530 C 207 NM_001014432.1 Transcript intron_variant - - - - - - rs2498805 14:105286243 C 196872 NR_024396.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1295 rs10150321 14:105296905 C - - - intergenic_variant - - - - - - rs12895706 14:105548415 T - - - intergenic_variant - - - - - - rs4983603 14:105800749 C - ENSR00001460566 RegulatoryFeature regulatory_region_variant - - - - - - rs4983603 14:105800749 C ENSESTG00000000536 ENSESTT00000001327 Transcript intron_variant - - - - - - rs4983603 14:105800749 C ENSESTG00000000536 ENSESTT00000001350 Transcript upstream_gene_variant - - - - - - DISTANCE=2013 rs4983603 14:105800749 C ENSESTG00000000536 ENSESTT00000001317 Transcript intron_variant - - - - - - rs4983603 14:105800749 C CCDS45178.2 CCDS45178.2 Transcript intron_variant - - - - - - rs4983603 14:105800749 C ENSESTG00000000536 ENSESTT00000001348 Transcript upstream_gene_variant - - - - - - DISTANCE=2013 rs4983603 14:105800749 C ENSESTG00000000536 ENSESTT00000001341 Transcript intron_variant - - - - - - rs4983603 14:105800749 C 23241 NM_001100913.2 Transcript intron_variant - - - - - - rs4983603 14:105800749 C 23241 NM_015197.3 Transcript intron_variant - - - - - - rs4983603 14:105800749 C ENSESTG00000000536 ENSESTT00000001340 Transcript intron_variant - - - - - - rs4983603 14:105800749 C CCDS32168.1 CCDS32168.1 Transcript intron_variant - - - - - - rs4983603 14:105800749 C 23241 NM_001243127.1 Transcript intron_variant - - - - - - rs4983603 14:105800749 C ENSESTG00000000536 ENSESTT00000001322 Transcript intron_variant - - - - - - rs9324084 14:105972133 G - - - intergenic_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000713 ENSESTT00000001722 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000756 ENSESTT00000001841 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000756 ENSESTT00000001824 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000756 ENSESTT00000001847 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000780 ENSESTT00000002061 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000780 ENSESTT00000002044 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000780 ENSESTT00000002077 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000780 ENSESTT00000002058 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000780 ENSESTT00000002060 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000707 ENSESTT00000001697 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000780 ENSESTT00000002111 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000780 ENSESTT00000002045 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000726 ENSESTT00000001733 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000780 ENSESTT00000002092 Transcript intron_variant - - - - - - rs56202511 14:106151374 T ENSESTG00000000780 ENSESTT00000002052 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000873 ENSESTT00000002120 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000002049 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000002061 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000002044 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000002058 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000002060 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000002026 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000001987 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000002045 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000002062 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs11624775 14:106293476 T ENSESTG00000000780 ENSESTT00000002052 Transcript intron_variant - - - - - - rs4774045 14:106468514 A ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs4774045 14:106468514 A ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs4774045 14:106468514 A ENSESTG00000035658 ENSESTT00000090085 Transcript upstream_gene_variant - - - - - - DISTANCE=2531 rs4774045 14:106468514 A ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs4774045 14:106468514 A 28473 NC_000014.8:IGHV1-3:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2730 rs4774045 14:106468514 A ENSESTG00000000780 ENSESTT00000001987 Transcript intron_variant - - - - - - rs4774045 14:106468514 A ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs4774045 14:106468514 A 28355 NC_000014.8:IGHVIII-2-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=536 rs4774045 14:106468514 A ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs4774045 14:106468514 A ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs7145339 14:106492108 C 28457 NC_000014.8:IGHV2-5:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2026 rs7145339 14:106492108 C ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs7145339 14:106492108 C ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs7145339 14:106492108 C 28354 NC_000014.8:IGHVIII-5-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3790 rs7145339 14:106492108 C ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs7145339 14:106492108 C ENSESTG00000000780 ENSESTT00000001987 Transcript intron_variant - - - - - - rs7145339 14:106492108 C ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs7145339 14:106492108 C ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs7145339 14:106492108 C ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs7141237 14:106494738 G 28457 NC_000014.8:IGHV2-5:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=161 rs7141237 14:106494738 G ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs7141237 14:106494738 G ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs7141237 14:106494738 G 28354 NC_000014.8:IGHVIII-5-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1160 rs7141237 14:106494738 G ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs7141237 14:106494738 G ENSESTG00000000780 ENSESTT00000001987 Transcript upstream_gene_variant - - - - - - DISTANCE=141 rs7141237 14:106494738 G ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs7141237 14:106494738 G ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs7141237 14:106494738 G ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs2879173 14:106506090 A ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs2879173 14:106506090 A ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs2879173 14:106506090 A ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs2879173 14:106506090 A ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs2879173 14:106506090 A ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs2879173 14:106506090 A 28353 NC_000014.8:IGHVIII-5-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3999 rs2879173 14:106506090 A ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs67469854 14:106515481 G ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs67469854 14:106515481 G ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs67469854 14:106515481 G ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs67469854 14:106515481 G 28452 NC_000014.8:IGHV3-7:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2917 rs67469854 14:106515481 G ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs67469854 14:106515481 G 28453 NC_000014.8:IGHV3-6:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3250 rs67469854 14:106515481 G ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs67469854 14:106515481 G ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs11160917 14:106522890 A ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs11160917 14:106522890 A ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs11160917 14:106522890 A ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs11160917 14:106522890 A ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs11160917 14:106522890 A ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs11160917 14:106522890 A 28452 NC_000014.8:IGHV3-7:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4037 rs11160917 14:106522890 A ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs4587858 14:106523505 G ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs4587858 14:106523505 G ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs4587858 14:106523505 G ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs4587858 14:106523505 G ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs4587858 14:106523505 G ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs4587858 14:106523505 G 28452 NC_000014.8:IGHV3-7:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4652 rs4587858 14:106523505 G ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs4773970 14:106553644 A ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs4773970 14:106553644 A ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs4773970 14:106553644 A ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs4773970 14:106553644 A ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs4773970 14:106553644 A ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs4773970 14:106553644 A ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs4773970 14:106553644 A 28451 NC_000014.8:IGHV3-9:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=915 rs4774064 14:106553741 G ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs4774064 14:106553741 G ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs4774064 14:106553741 G ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs4774064 14:106553741 G ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs4774064 14:106553741 G ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs4774064 14:106553741 G ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs4774064 14:106553741 G 28451 NC_000014.8:IGHV3-9:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1012 rs4774065 14:106557336 C 28456 NC_000014.8:IGHV2-10:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2204 rs4774065 14:106557336 C ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs4774065 14:106557336 C ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs4774065 14:106557336 C ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs4774065 14:106557336 C 28451 NC_000014.8:IGHV3-9:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4607 rs4774065 14:106557336 C ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs4774065 14:106557336 C ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs4774065 14:106557336 C ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs10135059 14:106558154 T ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs10135059 14:106558154 T 28456 NC_000014.8:IGHV2-10:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1386 rs10135059 14:106558154 T ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs10135059 14:106558154 T ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs10135059 14:106558154 T ENSESTG00000000780 ENSESTT00000001971 Transcript intron_variant - - - - - - rs10135059 14:106558154 T ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs10135059 14:106558154 T ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs11160922 14:106578952 T ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs11160922 14:106578952 T 28471 NC_000014.8:IGHV1-12:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=62 rs11160922 14:106578952 T ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs11160922 14:106578952 T ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs11160922 14:106578952 T ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs11160922 14:106578952 T ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs11160922 14:106578952 T 28352 NC_000014.8:IGHVIII-11-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1881 rs2338347 14:106580448 C ENSESTG00000000780 ENSESTT00000001940 Transcript intron_variant - - - - - - rs2338347 14:106580448 C 28471 NC_000014.8:IGHV1-12:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1145 rs2338347 14:106580448 C ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs2338347 14:106580448 C ENSESTG00000000780 ENSESTT00000001960 Transcript intron_variant - - - - - - rs2338347 14:106580448 C ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs2338347 14:106580448 C ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs2338347 14:106580448 C 28352 NC_000014.8:IGHVIII-11-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3377 rs12880979 14:106619691 A 28447 NC_000014.8:IGHV3-16:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2201 rs12880979 14:106619691 A 28376 NC_000014.8:IGHVII-15-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=530 rs12880979 14:106619691 A ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs12880979 14:106619691 A ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs12880979 14:106619691 A ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs12589211 14:106623600 C 28447 NC_000014.8:IGHV3-16:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1255 rs12589211 14:106623600 C 28376 NC_000014.8:IGHVII-15-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3109 rs12589211 14:106623600 C ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs12589211 14:106623600 C 28350 NC_000014.8:IGHVIII-16-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3836 rs12589211 14:106623600 C ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs12589211 14:106623600 C ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs12888429 14:106624360 C 28447 NC_000014.8:IGHV3-16:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2015 rs12888429 14:106624360 C 28376 NC_000014.8:IGHVII-15-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3869 rs12888429 14:106624360 C ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs12888429 14:106624360 C 28350 NC_000014.8:IGHVIII-16-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3076 rs12888429 14:106624360 C ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs12888429 14:106624360 C ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs1858705 14:106624936 C 28447 NC_000014.8:IGHV3-16:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2591 rs1858705 14:106624936 C 28376 NC_000014.8:IGHVII-15-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4445 rs1858705 14:106624936 C ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs1858705 14:106624936 C 28350 NC_000014.8:IGHVIII-16-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2500 rs1858705 14:106624936 C ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs1858705 14:106624936 C ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs8013539 14:106637268 C 28468 NC_000014.8:IGHV1-18:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4293 rs8013539 14:106637268 C ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs8013539 14:106637268 C ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs8013539 14:106637268 C ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs2157629 14:106641074 G 28468 NC_000014.8:IGHV1-18:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=487 rs2157629 14:106641074 G ENSESTG00000000780 ENSESTT00000001914 Transcript intron_variant - - - - - - rs2157629 14:106641074 G ENSESTG00000000780 ENSESTT00000001923 Transcript intron_variant - - - - - - rs2157629 14:106641074 G ENSESTG00000000780 ENSESTT00000001897 Transcript intron_variant - - - - - - rs2014247 14:106643404 T 28468 NC_000014.8:IGHV1-18:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1407 rs2014247 14:106643404 T ENSESTG00000000780 ENSESTT00000001914 Transcript upstream_gene_variant - - - - - - DISTANCE=1353 rs2014247 14:106643404 T ENSESTG00000000780 ENSESTT00000001923 Transcript upstream_gene_variant - - - - - - DISTANCE=1353 rs2014247 14:106643404 T ENSESTG00000000780 ENSESTT00000001897 Transcript upstream_gene_variant - - - - - - DISTANCE=1353 rs8013504 14:106654408 T 28446 NC_000014.8:IGHV3-19:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=747 rs10130534 14:106656692 T 28446 NC_000014.8:IGHV3-19:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3031 rs10134116 14:106658166 G 28446 NC_000014.8:IGHV3-19:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4505 rs7151105 14:106659609 A - - - intergenic_variant - - - - - - rs2338381 14:106659777 G - - - intergenic_variant - - - - - - rs6576133 14:106665142 A 28445 NC_000014.8:IGHV3-20:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2437 rs6576133 14:106665142 A 28375 NC_000014.8:IGHVII-20-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4323 rs6576134 14:106665193 A 28445 NC_000014.8:IGHV3-20:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2386 rs6576134 14:106665193 A 28375 NC_000014.8:IGHVII-20-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4272 rs8021673 14:106665267 A 28445 NC_000014.8:IGHV3-20:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2312 rs8021673 14:106665267 A 28375 NC_000014.8:IGHVII-20-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4198 rs11622917 14:106666798 C 28445 NC_000014.8:IGHV3-20:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=781 rs11622917 14:106666798 C 28375 NC_000014.8:IGHVII-20-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2667 rs12894507 14:106670016 T 28445 NC_000014.8:IGHV3-20:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1983 rs12894507 14:106670016 T 28375 NC_000014.8:IGHVII-20-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=51 rs10873562 14:106674335 T 28375 NC_000014.8:IGHVII-20-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4370 rs8013366 14:106675881 G - - - intergenic_variant - - - - - - rs1987415 14:106680599 A - - - intergenic_variant - - - - - - rs8012240 14:106681215 T - - - intergenic_variant - - - - - - rs7154767 14:106681665 G - - - intergenic_variant - - - - - - rs7141277 14:106682977 C - - - intergenic_variant - - - - - - rs7147494 14:106684057 A - - - intergenic_variant - - - - - - rs12889454 14:106685070 T - - - intergenic_variant - - - - - - rs2338376 14:106688153 T 28444 NC_000014.8:IGHV3-21:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3518 rs3944156 14:106688788 A 28444 NC_000014.8:IGHV3-21:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2883 rs7149498 14:106689395 A 28444 NC_000014.8:IGHV3-21:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2276 rs8009686 14:106692770 T - ENSR00001460589 RegulatoryFeature regulatory_region_variant - - - - - - rs8009686 14:106692770 T 28444 NC_000014.8:IGHV3-21:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=646 rs7142733 14:106698984 G - - - intergenic_variant - - - - - - rs7157411 14:106704776 G - - - intergenic_variant - - - - - - rs12895323 14:106705160 A - - - intergenic_variant - - - - - - rs10144802 14:106706454 A - - - intergenic_variant - - - - - - rs2879095 14:106708086 C - - - intergenic_variant - - - - - - rs10148698 14:106708227 T - - - intergenic_variant - - - - - - rs2040464 14:106709930 T 28443 NC_000014.8:IGHV3-22:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4430 rs11160934 14:106710418 T 28443 NC_000014.8:IGHV3-22:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3942 rs11160935 14:106710470 A 28443 NC_000014.8:IGHV3-22:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3890 rs10133263 14:106711903 A 28443 NC_000014.8:IGHV3-22:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2457 rs4773975 14:106712374 A 28443 NC_000014.8:IGHV3-22:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1986 rs10150478 14:106713595 A 28443 NC_000014.8:IGHV3-22:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=765 rs75335115 14:106720967 C 28349 NC_000014.8:IGHVIII-22-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=312 rs75335115 14:106720967 C 28374 NC_000014.8:IGHVII-22-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=746 rs75335115 14:106720967 C 28442 NC_000014.8:IGHV3-23:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4232 rs6576140 14:106721271 C 28349 NC_000014.8:IGHVIII-22-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=8 rs6576140 14:106721271 C 28374 NC_000014.8:IGHVII-22-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1050 rs6576140 14:106721271 C 28442 NC_000014.8:IGHV3-23:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3928 rs10149447 14:106748582 A 338004 NR_033375.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3616 rs10149447 14:106748582 A 28348 NC_000014.8:IGHVIII-25-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1578 rs10149447 14:106748582 A 28441 NC_000014.8:IGHV3-25:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2509 rs10149447 14:106748582 A ENSESTG00000035659 ENSESTT00000090088 Transcript downstream_gene_variant - - - - - - DISTANCE=3710 rs10138434 14:106748600 A 338004 NR_033375.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3634 rs10138434 14:106748600 A 28348 NC_000014.8:IGHVIII-25-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1560 rs10138434 14:106748600 A 28441 NC_000014.8:IGHV3-25:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2527 rs10138434 14:106748600 A ENSESTG00000035659 ENSESTT00000090088 Transcript downstream_gene_variant - - - - - - DISTANCE=3728 rs10149474 14:106748751 T 338004 NR_033375.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3785 rs10149474 14:106748751 T 28348 NC_000014.8:IGHVIII-25-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1409 rs10149474 14:106748751 T 28441 NC_000014.8:IGHV3-25:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2678 rs10149474 14:106748751 T ENSESTG00000035659 ENSESTT00000090088 Transcript downstream_gene_variant - - - - - - DISTANCE=3879 rs9788455 14:106750328 C 28348 NC_000014.8:IGHVIII-25-1:u_t_1 Transcript missense_variant 74 74 25 S/C tCc/tGc - rs9788455 14:106750328 C 28441 NC_000014.8:IGHV3-25:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4255 rs10135837 14:106751384 T 28348 NC_000014.8:IGHVIII-25-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=983 rs10151355 14:106752430 C 28348 NC_000014.8:IGHVIII-25-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2029 rs12100827 14:106752845 C 28455 NC_000014.8:IGHV2-26:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4804 rs12100827 14:106752845 C 28348 NC_000014.8:IGHVIII-25-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2444 rs8019037 14:106756131 T 28455 NC_000014.8:IGHV2-26:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1518 rs2338195 14:106758667 T 28455 NC_000014.8:IGHV2-26:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=575 rs6576144 14:106760965 G 28455 NC_000014.8:IGHV2-26:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2873 rs6576144 14:106760965 G 28347 NC_000014.8:IGHVIII-26-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4702 rs2338191 14:106761167 C 28455 NC_000014.8:IGHV2-26:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3075 rs2338191 14:106761167 C 28347 NC_000014.8:IGHVIII-26-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4500 rs2879126 14:106761254 C 28455 NC_000014.8:IGHV2-26:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3162 rs2879126 14:106761254 C 28347 NC_000014.8:IGHVIII-26-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4413 rs2879124 14:106761751 G 28455 NC_000014.8:IGHV2-26:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3659 rs2879124 14:106761751 G 28347 NC_000014.8:IGHVIII-26-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3916 rs7157321 14:106764650 C 28347 NC_000014.8:IGHVIII-26-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1017 rs12878919 14:106765454 T - ENSR00000100254 RegulatoryFeature regulatory_region_variant - - - - - - rs12878919 14:106765454 T 28347 NC_000014.8:IGHVIII-26-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=213 rs4773980 14:106766470 T 28373 NC_000014.8:IGHVII-26-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4441 rs4773980 14:106766470 T 28347 NC_000014.8:IGHVIII-26-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=497 rs10145251 14:106767265 T 28373 NC_000014.8:IGHVII-26-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3646 rs10145251 14:106767265 T 28347 NC_000014.8:IGHVIII-26-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1292 rs10137194 14:106769671 T 28373 NC_000014.8:IGHVII-26-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1240 rs10137194 14:106769671 T 28383 NC_000014.8:IGHV7-27:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4415 rs10137194 14:106769671 T 28347 NC_000014.8:IGHVIII-26-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3698 rs8003937 14:106771313 A 28373 NC_000014.8:IGHVII-26-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=90 rs8003937 14:106771313 A 28383 NC_000014.8:IGHV7-27:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2773 rs4774097 14:106772578 G 28373 NC_000014.8:IGHVII-26-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1355 rs4774097 14:106772578 G 28383 NC_000014.8:IGHV7-27:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1508 rs12886532 14:106776044 G 28400 NC_000014.8:IGHV4-28:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4467 rs12886532 14:106776044 G 28373 NC_000014.8:IGHVII-26-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4821 rs12886532 14:106776044 G 28383 NC_000014.8:IGHV7-27:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1545 rs10140427 14:106777972 C 28400 NC_000014.8:IGHV4-28:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2539 rs10140427 14:106777972 C 28383 NC_000014.8:IGHV7-27:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3473 rs4389061 14:106778553 A 28400 NC_000014.8:IGHV4-28:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1958 rs4389061 14:106778553 A 28383 NC_000014.8:IGHV7-27:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4054 rs4264300 14:106778772 C 28400 NC_000014.8:IGHV4-28:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1739 rs4264300 14:106778772 C 28383 NC_000014.8:IGHV7-27:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4273 rs1544319 14:106779055 C 28400 NC_000014.8:IGHV4-28:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1456 rs1544319 14:106779055 C 28383 NC_000014.8:IGHV7-27:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4556 rs1544318 14:106779102 C 28400 NC_000014.8:IGHV4-28:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1409 rs1544318 14:106779102 C 28383 NC_000014.8:IGHV7-27:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4603 rs2012850 14:106782220 A 28400 NC_000014.8:IGHV4-28:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1275 rs2012850 14:106782220 A 28372 NC_000014.8:IGHVII-28-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3466 rs7151504 14:106784987 A 28400 NC_000014.8:IGHV4-28:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4042 rs7151504 14:106784987 A 28372 NC_000014.8:IGHVII-28-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=699 rs7151504 14:106784987 A 28440 NC_000014.8:IGHV3-29:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2371 rs8011602 14:106803544 G 28396 NC_000014.8:IGHV4-31:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1663 rs8011602 14:106803544 G 28371 NC_000014.8:IGHVII-30-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4669 rs8011602 14:106803544 G ENSESTG00000035669 ENSESTT00000090103 Transcript intron_variant - - - - - - rs8011602 14:106803544 G 28438 NC_000014.8:IGHV3-30-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2787 rs3858876 14:106805772 G - ENSR00000424832 RegulatoryFeature regulatory_region_variant - - - - - - rs3858876 14:106805772 G 28396 NC_000014.8:IGHV4-31:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=128 rs3858876 14:106805772 G 28370 NC_000014.8:IGHVII-31-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4769 rs3858876 14:106805772 G ENSESTG00000035669 ENSESTT00000090103 Transcript intron_variant - - - - - - rs8009391 14:106807085 T 28396 NC_000014.8:IGHV4-31:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1441 rs8009391 14:106807085 T 28435 NC_000014.8:IGHV3-32:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4986 rs8009391 14:106807085 T 28370 NC_000014.8:IGHVII-31-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3456 rs8009391 14:106807085 T ENSESTG00000035669 ENSESTT00000090103 Transcript intron_variant - - - - - - rs7160932 14:106819562 C 28369 NC_000014.8:IGHVII-33-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3759 rs7160932 14:106819562 C 28434 NC_000014.8:IGHV3-33:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3389 rs7160932 14:106819562 C ENSESTG00000035669 ENSESTT00000090103 Transcript upstream_gene_variant - - - - - - DISTANCE=3370 rs12891040 14:106825673 G 28369 NC_000014.8:IGHVII-33-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2079 rs12891040 14:106825673 G ENSESTG00000035664 ENSESTT00000090101 Transcript downstream_gene_variant - - - - - - DISTANCE=3943 rs12891040 14:106825673 G 28395 NC_000014.8:IGHV4-34:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3919 rs12891040 14:106825673 G 28433 NC_000014.8:IGHV3-33-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=196 rs11620712 14:106835356 C 28382 NC_000014.8:IGHV7-34-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1692 rs11620712 14:106835356 C ENSESTG00000035664 ENSESTT00000090101 Transcript intron_variant - - - - - - rs2027914 14:106839600 T 100288568 XM_002343297.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2611 rs2027914 14:106839600 T ENSESTG00000035664 ENSESTT00000090101 Transcript intron_variant - - - - - - rs2338128 14:106841047 A 28432 NC_000014.8:IGHV3-35:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4274 rs2338128 14:106841047 A 100288568 XM_002343297.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1164 rs2338128 14:106841047 A ENSESTG00000035664 ENSESTT00000090101 Transcript intron_variant - - - - - - rs10129623 14:106844860 T 28431 NC_000014.8:IGHV3-36:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3820 rs10129623 14:106844860 T 28432 NC_000014.8:IGHV3-35:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=461 rs10129623 14:106844860 T 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs10129623 14:106844860 T ENSESTG00000035664 ENSESTT00000090101 Transcript intron_variant - - - - - - rs12884890 14:106846077 T 28431 NC_000014.8:IGHV3-36:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2603 rs12884890 14:106846077 T 28432 NC_000014.8:IGHV3-35:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=303 rs12884890 14:106846077 T 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs12884890 14:106846077 T ENSESTG00000035664 ENSESTT00000090101 Transcript intron_variant - - - - - - rs12895463 14:106847525 G 28431 NC_000014.8:IGHV3-36:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1155 rs12895463 14:106847525 G 28432 NC_000014.8:IGHV3-35:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1751 rs12895463 14:106847525 G 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs12895463 14:106847525 G ENSESTG00000035664 ENSESTT00000090101 Transcript intron_variant - - - - - - rs10139672 14:106848075 G 28431 NC_000014.8:IGHV3-36:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=605 rs10139672 14:106848075 G 28432 NC_000014.8:IGHV3-35:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2301 rs10139672 14:106848075 G 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs10139672 14:106848075 G ENSESTG00000035664 ENSESTT00000090101 Transcript intron_variant - - - - - - rs10139672 14:106848075 G 28430 NC_000014.8:IGHV3-37:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4502 rs7400802 14:106853604 T 28431 NC_000014.8:IGHV3-36:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4462 rs7400802 14:106853604 T 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs7400802 14:106853604 T ENSESTG00000035664 ENSESTT00000090101 Transcript intron_variant - - - - - - rs7400802 14:106853604 T 28430 NC_000014.8:IGHV3-37:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=578 rs6576158 14:106854412 A 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs6576158 14:106854412 A ENSESTG00000035664 ENSESTT00000090101 Transcript intron_variant - - - - - - rs6576158 14:106854412 A 28430 NC_000014.8:IGHV3-37:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1386 rs11846968 14:106864703 A 28429 NC_000014.8:IGHV3-38:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1704 rs11846968 14:106864703 A 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs12589860 14:106867623 A 28429 NC_000014.8:IGHV3-38:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=767 rs12589860 14:106867623 A 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs7401481 14:106868012 T 28429 NC_000014.8:IGHV3-38:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1156 rs7401481 14:106868012 T 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs12432524 14:106869223 T 28429 NC_000014.8:IGHV3-38:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2367 rs12432524 14:106869223 T 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs12432524 14:106869223 T 28346 NC_000014.8:IGHVIII-38-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4712 rs10136025 14:106869392 T 28429 NC_000014.8:IGHV3-38:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2536 rs10136025 14:106869392 T 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs10136025 14:106869392 T 28346 NC_000014.8:IGHVIII-38-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4543 rs8021361 14:106870882 A 28429 NC_000014.8:IGHV3-38:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4026 rs8021361 14:106870882 A 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs8021361 14:106870882 A 28346 NC_000014.8:IGHVIII-38-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3053 rs8021361 14:106870882 A ENSESTG00000035660 ENSESTT00000090091 Transcript upstream_gene_variant - - - - - - DISTANCE=4412 rs10873566 14:106872250 A 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs10873566 14:106872250 A 28346 NC_000014.8:IGHVIII-38-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1685 rs10873566 14:106872250 A ENSESTG00000035660 ENSESTT00000090091 Transcript upstream_gene_variant - - - - - - DISTANCE=3044 rs2338123 14:106876900 T 28381 NC_000014.8:IGHV7-40:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4364 rs2338123 14:106876900 T 28394 NC_000014.8:IGHV4-39:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=717 rs2338123 14:106876900 T 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs2338123 14:106876900 T 28346 NC_000014.8:IGHVIII-38-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2673 rs2338123 14:106876900 T ENSESTG00000035660 ENSESTT00000090091 Transcript intron_variant - - - - - - rs8016289 14:106877262 A 28381 NC_000014.8:IGHV7-40:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4002 rs8016289 14:106877262 A 28394 NC_000014.8:IGHV4-39:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=355 rs8016289 14:106877262 A 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs8016289 14:106877262 A 28346 NC_000014.8:IGHVIII-38-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3035 rs8016289 14:106877262 A ENSESTG00000035660 ENSESTT00000090091 Transcript intron_variant - - - - - - rs976225 14:106878434 A 28381 NC_000014.8:IGHV7-40:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2830 rs976225 14:106878434 A 28394 NC_000014.8:IGHV4-39:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=379 rs976225 14:106878434 A 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs976225 14:106878434 A 28346 NC_000014.8:IGHVIII-38-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4207 rs976225 14:106878434 A ENSESTG00000035660 ENSESTT00000090091 Transcript intron_variant - - - - - - rs11160963 14:106879613 G 28381 NC_000014.8:IGHV7-40:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1651 rs11160963 14:106879613 G 28394 NC_000014.8:IGHV4-39:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1558 rs11160963 14:106879613 G 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs11160963 14:106879613 G ENSESTG00000035660 ENSESTT00000090091 Transcript intron_variant - - - - - - rs8022371 14:106879876 G 28381 NC_000014.8:IGHV7-40:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1388 rs8022371 14:106879876 G 28394 NC_000014.8:IGHV4-39:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1821 rs8022371 14:106879876 G 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs8022371 14:106879876 G ENSESTG00000035660 ENSESTT00000090091 Transcript intron_variant - - - - - - rs8007277 14:106880503 G 28381 NC_000014.8:IGHV7-40:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=761 rs8007277 14:106880503 G 28394 NC_000014.8:IGHV4-39:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2448 rs8007277 14:106880503 G 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs8007277 14:106880503 G ENSESTG00000035660 ENSESTT00000090091 Transcript intron_variant - - - - - - rs55849186 14:106882804 G 28381 NC_000014.8:IGHV7-40:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1338 rs55849186 14:106882804 G 28394 NC_000014.8:IGHV4-39:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4749 rs55849186 14:106882804 G 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs55849186 14:106882804 G ENSESTG00000035660 ENSESTT00000090091 Transcript downstream_gene_variant - - - - - - DISTANCE=2147 rs10147400 14:106891180 T 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs7142421 14:106892380 C - ENSR00000652869 RegulatoryFeature regulatory_region_variant - - - - - - rs7142421 14:106892380 C 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs7142421 14:106892380 C 28368 NC_000014.8:IGHVII-40-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4465 rs756593 14:106898830 G - ENSR00000652870 RegulatoryFeature regulatory_region_variant - - - - - - rs756593 14:106898830 G 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs756593 14:106898830 G 28428 NC_000014.8:IGHV3-41:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=210 rs756593 14:106898830 G 28368 NC_000014.8:IGHVII-40-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1909 rs4494448 14:106900710 T 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs4494448 14:106900710 T 28428 NC_000014.8:IGHV3-41:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1216 rs4494448 14:106900710 T 28368 NC_000014.8:IGHVII-40-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3789 rs4393471 14:106901114 A 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs4393471 14:106901114 A 28428 NC_000014.8:IGHV3-41:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1620 rs4393471 14:106901114 A 28368 NC_000014.8:IGHVII-40-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4193 rs1858698 14:106901914 A 100288568 XM_002343297.3 Transcript intron_variant - - - - - - rs1858698 14:106901914 A 28428 NC_000014.8:IGHV3-41:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2420 rs1858698 14:106901914 A 28368 NC_000014.8:IGHVII-40-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4993 rs10873572 14:106914628 T 28427 NC_000014.8:IGHV3-42:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4551 rs4774130 14:106915172 C 28427 NC_000014.8:IGHV3-42:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4007 rs10131899 14:106915859 G - ENSR00001460592 RegulatoryFeature regulatory_region_variant - - - - - - rs10131899 14:106915859 G 28427 NC_000014.8:IGHV3-42:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3320 rs4773988 14:106916459 C 28427 NC_000014.8:IGHV3-42:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2720 rs10134484 14:106922028 T 28426 NC_000014.8:IGHV3-43:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4159 rs10134484 14:106922028 T 28427 NC_000014.8:IGHV3-42:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2415 rs8011056 14:106925252 C 28367 NC_000014.8:IGHVII-43-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3463 rs8011056 14:106925252 C 28426 NC_000014.8:IGHV3-43:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=935 rs11160974 14:106925755 A 28367 NC_000014.8:IGHVII-43-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2960 rs11160974 14:106925755 A 28426 NC_000014.8:IGHV3-43:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=432 rs2027907 14:106928158 C 28367 NC_000014.8:IGHVII-43-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=557 rs2027907 14:106928158 C 28426 NC_000014.8:IGHV3-43:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1514 rs9324086 14:106930097 A 28367 NC_000014.8:IGHVII-43-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1174 rs9324086 14:106930097 A 28426 NC_000014.8:IGHV3-43:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3453 rs9324086 14:106930097 A 28345 NC_000014.8:IGHVIII-44:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4126 rs9324087 14:106930197 A 28367 NC_000014.8:IGHVII-43-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1274 rs9324087 14:106930197 A 28426 NC_000014.8:IGHV3-43:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3553 rs9324087 14:106930197 A 28345 NC_000014.8:IGHVIII-44:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4026 rs2005646 14:106934063 C - ENSR00000424844 RegulatoryFeature regulatory_region_variant - - - - - - rs2005646 14:106934063 C 338005 NR_027457.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4392 rs2005646 14:106934063 C ENSESTG00000035661 ENSESTT00000090092 Transcript upstream_gene_variant - - - - - - DISTANCE=4392 rs2005646 14:106934063 C ENSESTG00000035661 ENSESTT00000090093 Transcript upstream_gene_variant - - - - - - DISTANCE=4403 rs2005646 14:106934063 C 28345 NC_000014.8:IGHVIII-44:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=160 rs28682542 14:106935675 C 338005 NR_027457.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2780 rs28682542 14:106935675 C ENSESTG00000035661 ENSESTT00000090092 Transcript upstream_gene_variant - - - - - - DISTANCE=2780 rs28682542 14:106935675 C ENSESTG00000035661 ENSESTT00000090093 Transcript upstream_gene_variant - - - - - - DISTANCE=2791 rs28682542 14:106935675 C 28345 NC_000014.8:IGHVIII-44:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1276 rs7146103 14:106946187 A 338005 NR_027457.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7146103 14:106946187 A ENSESTG00000035661 ENSESTT00000090092 Transcript intron_variant - - - - - - rs7146103 14:106946187 A 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3972 rs7146103 14:106946187 A ENSESTG00000035661 ENSESTT00000090093 Transcript intron_variant - - - - - - rs7146103 14:106946187 A 28337 NC_000014.8:IGHVIV-44-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=410 rs2427686 14:106946720 T 338005 NR_027457.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2427686 14:106946720 T ENSESTG00000035661 ENSESTT00000090092 Transcript downstream_gene_variant - - - - - - DISTANCE=226 rs2427686 14:106946720 T 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3439 rs2427686 14:106946720 T ENSESTG00000035661 ENSESTT00000090093 Transcript intron_variant - - - - - - rs2427686 14:106946720 T 28337 NC_000014.8:IGHVIV-44-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=943 rs10135651 14:106947174 T 338005 NR_027457.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10135651 14:106947174 T ENSESTG00000035661 ENSESTT00000090092 Transcript downstream_gene_variant - - - - - - DISTANCE=680 rs10135651 14:106947174 T 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2985 rs10135651 14:106947174 T ENSESTG00000035661 ENSESTT00000090093 Transcript intron_variant - - - - - - rs10135651 14:106947174 T 28337 NC_000014.8:IGHVIV-44-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1397 rs11627759 14:106947219 A 338005 NR_027457.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11627759 14:106947219 A ENSESTG00000035661 ENSESTT00000090092 Transcript downstream_gene_variant - - - - - - DISTANCE=725 rs11627759 14:106947219 A 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2940 rs11627759 14:106947219 A ENSESTG00000035661 ENSESTT00000090093 Transcript intron_variant - - - - - - rs11627759 14:106947219 A 28337 NC_000014.8:IGHVIV-44-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1442 rs11623200 14:106947288 A 338005 NR_027457.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11623200 14:106947288 A ENSESTG00000035661 ENSESTT00000090092 Transcript downstream_gene_variant - - - - - - DISTANCE=794 rs11623200 14:106947288 A 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2871 rs11623200 14:106947288 A ENSESTG00000035661 ENSESTT00000090093 Transcript intron_variant - - - - - - rs11623200 14:106947288 A 28337 NC_000014.8:IGHVIV-44-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1511 rs10873579 14:106947566 G 338005 NR_027457.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10873579 14:106947566 G ENSESTG00000035661 ENSESTT00000090092 Transcript downstream_gene_variant - - - - - - DISTANCE=1072 rs10873579 14:106947566 G 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2593 rs10873579 14:106947566 G ENSESTG00000035661 ENSESTT00000090093 Transcript intron_variant - - - - - - rs10873579 14:106947566 G 28337 NC_000014.8:IGHVIV-44-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1789 rs2078694 14:106947891 G - ENSR00001460594 RegulatoryFeature regulatory_region_variant - - - - - - rs2078694 14:106947891 G 338005 NR_027457.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2078694 14:106947891 G ENSESTG00000035661 ENSESTT00000090092 Transcript downstream_gene_variant - - - - - - DISTANCE=1397 rs2078694 14:106947891 G 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2268 rs2078694 14:106947891 G ENSESTG00000035661 ENSESTT00000090093 Transcript intron_variant - - - - - - rs2078694 14:106947891 G 28337 NC_000014.8:IGHVIV-44-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2114 rs8003770 14:106954255 A 338005 NR_027457.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2726 rs8003770 14:106954255 A 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3860 rs8003770 14:106954255 A ENSESTG00000035661 ENSESTT00000090093 Transcript downstream_gene_variant - - - - - - DISTANCE=3714 rs11626351 14:106954910 G 338005 NR_027457.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3381 rs11626351 14:106954910 G 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4515 rs11626351 14:106954910 G ENSESTG00000035661 ENSESTT00000090093 Transcript downstream_gene_variant - - - - - - DISTANCE=4369 rs11626353 14:106954983 T 338005 NR_027457.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3454 rs11626353 14:106954983 T 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4588 rs11626353 14:106954983 T ENSESTG00000035661 ENSESTT00000090093 Transcript downstream_gene_variant - - - - - - DISTANCE=4442 rs7493038 14:106955093 G 338005 NR_027457.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3564 rs7493038 14:106955093 G 28366 NC_000014.8:IGHVII-44-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4698 rs7493038 14:106955093 G ENSESTG00000035661 ENSESTT00000090093 Transcript downstream_gene_variant - - - - - - DISTANCE=4552 rs12895484 14:106957048 T - - - intergenic_variant - - - - - - rs2337938 14:106958377 A ENSESTG00000035663 ENSESTT00000090095 Transcript upstream_gene_variant - - - - - - DISTANCE=4827 rs2337938 14:106958377 A 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4552 rs756590 14:106958445 A ENSESTG00000035663 ENSESTT00000090095 Transcript upstream_gene_variant - - - - - - DISTANCE=4759 rs756590 14:106958445 A 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4484 rs8021231 14:106958508 T ENSESTG00000035663 ENSESTT00000090095 Transcript upstream_gene_variant - - - - - - DISTANCE=4696 rs8021231 14:106958508 T 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4421 rs2467925 14:106959994 G ENSESTG00000035663 ENSESTT00000090095 Transcript upstream_gene_variant - - - - - - DISTANCE=3210 rs2467925 14:106959994 G 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2935 rs2467926 14:106959997 A ENSESTG00000035663 ENSESTT00000090095 Transcript upstream_gene_variant - - - - - - DISTANCE=3207 rs2467926 14:106959997 A 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2932 rs11160983 14:106960087 G ENSESTG00000035663 ENSESTT00000090095 Transcript upstream_gene_variant - - - - - - DISTANCE=3117 rs11160983 14:106960087 G 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2842 rs2427682 14:106960207 A ENSESTG00000035663 ENSESTT00000090095 Transcript upstream_gene_variant - - - - - - DISTANCE=2997 rs2427682 14:106960207 A 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2722 rs2467922 14:106963752 A 28465 NC_000014.8:IGHV1-46:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3295 rs2467922 14:106963752 A ENSESTG00000035663 ENSESTT00000090095 Transcript intron_variant - - - - - - rs2467922 14:106963752 A 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=386 rs2467920 14:106964127 G 28465 NC_000014.8:IGHV1-46:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2920 rs2467920 14:106964127 G ENSESTG00000035663 ENSESTT00000090095 Transcript intron_variant - - - - - - rs2467920 14:106964127 G 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=761 rs1557581 14:106965523 T 28465 NC_000014.8:IGHV1-46:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1524 rs1557581 14:106965523 T ENSESTG00000035663 ENSESTT00000090095 Transcript downstream_gene_variant - - - - - - DISTANCE=764 rs1557581 14:106965523 T 28466 NC_000014.8:IGHV1-45:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2157 rs2583348 14:107012766 T - ENSR00001460597 RegulatoryFeature regulatory_region_variant - - - - - - rs2583348 14:107012766 T 28423 NC_000014.8:IGHV3-49:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=170 rs2252062 14:107018398 C 28364 NC_000014.8:IGHVII-49-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1918 rs2252062 14:107018398 C 28422 NC_000014.8:IGHV3-50:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3690 rs2583353 14:107023974 G 28364 NC_000014.8:IGHVII-49-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3388 rs2583353 14:107023974 G 28422 NC_000014.8:IGHV3-50:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1431 rs2516935 14:107027018 T 28422 NC_000014.8:IGHV3-50:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4475 rs1024354 14:107032220 G 28388 NC_000014.8:IGHV5-51:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2507 rs1024353 14:107032329 G 28388 NC_000014.8:IGHV5-51:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2398 rs1024352 14:107032332 G 28388 NC_000014.8:IGHV5-51:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2395 rs1024351 14:107032477 G 28388 NC_000014.8:IGHV5-51:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2250 rs2516930 14:107032603 C 28388 NC_000014.8:IGHV5-51:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2124 rs1018839 14:107032912 T 28388 NC_000014.8:IGHV5-51:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1815 rs2731186 14:107037237 C 28388 NC_000014.8:IGHV5-51:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2075 rs2731186 14:107037237 C 28363 NC_000014.8:IGHVII-51-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3461 rs2731186 14:107037237 C 28343 NC_000014.8:IGHVIII-51-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2251 rs756595 14:107039624 C 28388 NC_000014.8:IGHV5-51:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4462 rs756595 14:107039624 C 28421 NC_000014.8:IGHV3-52:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2736 rs756595 14:107039624 C 28363 NC_000014.8:IGHVII-51-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1074 rs756595 14:107039624 C 28343 NC_000014.8:IGHVIII-51-1:u_t_1 Transcript synonymous_variant 171 171 57 V gtA/gtG - rs2516929 14:107040250 A 28421 NC_000014.8:IGHV3-52:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2110 rs2516929 14:107040250 A 28363 NC_000014.8:IGHVII-51-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=448 rs2516929 14:107040250 A 28343 NC_000014.8:IGHVIII-51-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=456 rs2583346 14:107040365 A 28421 NC_000014.8:IGHV3-52:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1995 rs2583346 14:107040365 A 28363 NC_000014.8:IGHVII-51-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=333 rs2583346 14:107040365 A 28343 NC_000014.8:IGHVIII-51-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=571 rs2027913 14:107045304 T 28420 NC_000014.8:IGHV3-53:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3366 rs2027913 14:107045304 T 28421 NC_000014.8:IGHV3-52:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2494 rs2027913 14:107045304 T 28363 NC_000014.8:IGHVII-51-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4344 rs2027911 14:107045402 A 28420 NC_000014.8:IGHV3-53:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3268 rs2027911 14:107045402 A 28421 NC_000014.8:IGHV3-52:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2592 rs2027911 14:107045402 A 28363 NC_000014.8:IGHVII-51-2:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4442 rs2516926 14:107046425 A 28420 NC_000014.8:IGHV3-53:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2245 rs2516926 14:107046425 A 28421 NC_000014.8:IGHV3-52:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3615 rs2516921 14:107049249 C 28420 NC_000014.8:IGHV3-53:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=129 rs2516915 14:107051668 A 28420 NC_000014.8:IGHV3-53:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2548 rs2516915 14:107051668 A 28362 NC_000014.8:IGHVII-53-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3999 rs2583359 14:107063037 A 28380 NC_000014.8:IGHV7-56:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2735 rs2583359 14:107063037 A 28393 NC_000014.8:IGHV4-55:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=476 rs2583360 14:107066435 G 28380 NC_000014.8:IGHV7-56:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=229 rs2583360 14:107066435 G 28393 NC_000014.8:IGHV4-55:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3874 rs2213893 14:107069121 G 28380 NC_000014.8:IGHV7-56:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2915 rs2516906 14:107070541 T 28418 NC_000014.8:IGHV3-57:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4381 rs2516906 14:107070541 T 28380 NC_000014.8:IGHV7-56:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4335 rs2583337 14:107070551 T 28418 NC_000014.8:IGHV3-57:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4371 rs2583337 14:107070551 T 28380 NC_000014.8:IGHV7-56:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4345 rs2078695 14:107072354 C 28418 NC_000014.8:IGHV3-57:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2568 rs2583334 14:107073674 A 28418 NC_000014.8:IGHV3-57:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1248 rs2583334 14:107073674 A 28464 NC_000014.8:IGHV1-58:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4697 rs2014866 14:107075632 G 28418 NC_000014.8:IGHV3-57:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=405 rs2014866 14:107075632 G 28464 NC_000014.8:IGHV1-58:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2739 rs2583326 14:107080551 T 28392 NC_000014.8:IGHV4-59:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2703 rs2583326 14:107080551 T 28464 NC_000014.8:IGHV1-58:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1743 rs12897804 14:107093209 A 28391 NC_000014.8:IGHV4-61:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1915 rs12897804 14:107093209 A 28361 NC_000014.8:IGHVII-60-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=501 rs2583298 14:107097238 A 28391 NC_000014.8:IGHV4-61:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1677 rs2583298 14:107097238 A 28416 NC_000014.8:IGHV3-62:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1895 rs2583298 14:107097238 A 28361 NC_000014.8:IGHVII-60-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3260 rs2583293 14:107103156 A 28416 NC_000014.8:IGHV3-62:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3568 rs2583293 14:107103156 A 28360 NC_000014.8:IGHVII-62-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3364 rs2516891 14:107103576 A 28416 NC_000014.8:IGHV3-62:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3988 rs2516891 14:107103576 A 28415 NC_000014.8:IGHV3-63:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4652 rs2516891 14:107103576 A 28360 NC_000014.8:IGHVII-62-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2944 rs4992201 14:107105387 T 28415 NC_000014.8:IGHV3-63:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2841 rs4992201 14:107105387 T 28360 NC_000014.8:IGHVII-62-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1133 rs4992200 14:107105415 T 28415 NC_000014.8:IGHV3-63:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2813 rs4992200 14:107105415 T 28360 NC_000014.8:IGHVII-62-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1105 rs4990859 14:107106777 A 28415 NC_000014.8:IGHV3-63:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1451 rs4990859 14:107106777 A 28360 NC_000014.8:IGHVII-62-1:u_t_1 Transcript missense_variant 16 16 6 P/S Cca/Tca - rs4990860 14:107106843 A 28415 NC_000014.8:IGHV3-63:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1385 rs4990860 14:107106843 A 28360 NC_000014.8:IGHVII-62-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=51 rs1811154 14:107110778 G 28414 NC_000014.8:IGHV3-64:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2961 rs1811154 14:107110778 G 28415 NC_000014.8:IGHV3-63:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2083 rs1811154 14:107110778 G 28360 NC_000014.8:IGHVII-62-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3986 rs2247821 14:107114747 C 28414 NC_000014.8:IGHV3-64:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=553 rs2516868 14:107115419 T 28414 NC_000014.8:IGHV3-64:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1225 rs2583304 14:107115436 A 28414 NC_000014.8:IGHV3-64:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1242 rs7146513 14:107178532 G 28411 NC_000014.8:IGHV3-71:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4864 rs7146513 14:107178532 G 28454 NC_000014.8:IGHV2-70:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=287 rs11161009 14:107187944 T 28411 NC_000014.8:IGHV3-71:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4087 rs8022331 14:107189981 T - - - intergenic_variant - - - - - - rs2337405 14:107191638 T - - - intergenic_variant - - - - - - rs8005284 14:107194297 G 28410 NC_000014.8:IGHV3-72:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4633 rs1987970 14:107198866 G - ENSR00000652880 RegulatoryFeature regulatory_region_variant - - - - - - rs1987970 14:107198866 G - MA0139.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=7;MOTIF_NAME=Jaspar_Matrix_CTCF:MA0139.1;HIGH_INF_POS=N;MOTIF_SCORE_CHANGE=0.033 rs1987970 14:107198866 G 28410 NC_000014.8:IGHV3-72:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=64 rs8010634 14:107214202 G 28409 NC_000014.8:IGHV3-73:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2811 rs8010634 14:107214202 G 28408 NC_000014.8:IGHV3-74:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4472 rs10782503 14:107242351 G 28339 NC_000014.8:IGHVIII-76-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2055 rs2157620 14:107247958 C - - - intergenic_variant - - - - - - rs6576238 14:107248227 G - - - intergenic_variant - - - - - - rs6576239 14:107248232 T - - - intergenic_variant - - - - - - rs2105993 14:107249506 C - - - intergenic_variant - - - - - - rs2078692 14:107250658 G - - - intergenic_variant - - - - - - rs2008039 14:107269589 A 28356 NC_000014.8:IGHVII-78-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4247 rs2187995 14:107286032 C 28378 NC_000014.8:IGHV7-81:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2806 rs2187995 14:107286032 C 28338 NC_000014.8:IGHVIII-82:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1728 rs2187995 14:107286032 C 28390 NC_000014.8:IGHV4-80:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4638 rs8018213 14:107287486 G - ENSR00000100286 RegulatoryFeature regulatory_region_variant - - - - - - rs8018213 14:107287486 G 28378 NC_000014.8:IGHV7-81:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4260 rs8018213 14:107287486 G 28338 NC_000014.8:IGHVIII-82:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=274 rs8019483 14:107287508 G - ENSR00000100286 RegulatoryFeature regulatory_region_variant - - - - - - rs8019483 14:107287508 G 28378 NC_000014.8:IGHV7-81:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4282 rs8019483 14:107287508 G 28338 NC_000014.8:IGHVIII-82:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=252 rs8018521 14:107287560 G - ENSR00000100286 RegulatoryFeature regulatory_region_variant - - - - - - rs8018521 14:107287560 G - MA0139.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=17;MOTIF_NAME=Jaspar_Matrix_CTCF:MA0139.1;HIGH_INF_POS=N;MOTIF_SCORE_CHANGE=0.006 rs8018521 14:107287560 G 28378 NC_000014.8:IGHV7-81:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4334 rs8018521 14:107287560 G 28338 NC_000014.8:IGHVIII-82:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=200 rs2337451 14:107289205 A 28338 NC_000014.8:IGHVIII-82:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1154 rs4247058 15:21938136 T 646214 NR_027053.1 Transcript non_coding_exon_variant,nc_transcript_variant 2604 - - - - - rs1835205 15:22406355 C ENSESTG00000005824 ENSESTT00000014754 Transcript upstream_gene_variant - - - - - - DISTANCE=2054 rs480140 15:22489219 A - - - intergenic_variant - - - - - - rs6606806 15:22937645 A ENSESTG00000005892 ENSESTT00000014976 Transcript intron_variant - - - - - - rs6606806 15:22937645 A ENSESTG00000025920 ENSESTT00000065468 Transcript downstream_gene_variant - - - - - - DISTANCE=1764 rs6606806 15:22937645 A CCDS10009.1 CCDS10009.1 Transcript intron_variant - - - - - - rs6606806 15:22937645 A ENSESTG00000025996 ENSESTT00000065894 Transcript upstream_gene_variant - - - - - - DISTANCE=1528 rs6606806 15:22937645 A ENSESTG00000025996 ENSESTT00000065852 Transcript intron_variant - - - - - - rs6606806 15:22937645 A ENSESTG00000025996 ENSESTT00000065873 Transcript intron_variant - - - - - - rs6606806 15:22937645 A 23191 NM_014608.2 Transcript intron_variant - - - - - - rs6606806 15:22937645 A ENSESTG00000005892 ENSESTT00000014989 Transcript downstream_gene_variant - - - - - - DISTANCE=3854 rs10908261 15:23035176 T - ENSR00000404794 RegulatoryFeature regulatory_region_variant - - - - - - rs10908261 15:23035176 T 81614 NM_001008894.2 Transcript upstream_gene_variant - - - - - - DISTANCE=749 rs10908261 15:23035176 T 81614 NM_001008892.2 Transcript upstream_gene_variant - - - - - - DISTANCE=749 rs10908261 15:23035176 T 81614 NM_030922.6 Transcript upstream_gene_variant - - - - - - DISTANCE=749 rs10908261 15:23035176 T 81614 NM_001008860.2 Transcript upstream_gene_variant - - - - - - DISTANCE=749 rs10908261 15:23035176 T ENSESTG00000026805 ENSESTT00000067653 Transcript upstream_gene_variant - - - - - - DISTANCE=898 rs10908261 15:23035176 T ENSESTG00000026805 ENSESTT00000067600 Transcript upstream_gene_variant - - - - - - DISTANCE=752 rs10908261 15:23035176 T ENSESTG00000026805 ENSESTT00000067711 Transcript upstream_gene_variant - - - - - - DISTANCE=1842 rs10908261 15:23035176 T 81614 NM_001184888.1 Transcript upstream_gene_variant - - - - - - DISTANCE=749 rs10908261 15:23035176 T 81614 NM_001184889.1 Transcript upstream_gene_variant - - - - - - DISTANCE=749 rs10908261 15:23035176 T ENSESTG00000026805 ENSESTT00000067628 Transcript upstream_gene_variant - - - - - - DISTANCE=768 rs10908261 15:23035176 T ENSESTG00000026805 ENSESTT00000067705 Transcript upstream_gene_variant - - - - - - DISTANCE=919 rs10908261 15:23035176 T ENSESTG00000026805 ENSESTT00000067647 Transcript upstream_gene_variant - - - - - - DISTANCE=775 rs919945 15:23037404 T - ENSR00000236013 RegulatoryFeature regulatory_region_variant - - - - - - rs919945 15:23037404 T 81614 NM_001008894.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2977 rs919945 15:23037404 T 81614 NM_001008892.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2977 rs919945 15:23037404 T 81614 NM_030922.6 Transcript upstream_gene_variant - - - - - - DISTANCE=2977 rs919945 15:23037404 T 81614 NM_001008860.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2977 rs919945 15:23037404 T ENSESTG00000026805 ENSESTT00000067653 Transcript upstream_gene_variant - - - - - - DISTANCE=3126 rs919945 15:23037404 T ENSESTG00000026805 ENSESTT00000067600 Transcript upstream_gene_variant - - - - - - DISTANCE=2980 rs919945 15:23037404 T ENSESTG00000026805 ENSESTT00000067711 Transcript upstream_gene_variant - - - - - - DISTANCE=4070 rs919945 15:23037404 T 81614 NM_001184888.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2977 rs919945 15:23037404 T 81614 NM_001184889.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2977 rs919945 15:23037404 T ENSESTG00000026805 ENSESTT00000067628 Transcript upstream_gene_variant - - - - - - DISTANCE=2996 rs919945 15:23037404 T ENSESTG00000026805 ENSESTT00000067705 Transcript upstream_gene_variant - - - - - - DISTANCE=3147 rs919945 15:23037404 T ENSESTG00000026805 ENSESTT00000067647 Transcript upstream_gene_variant - - - - - - DISTANCE=3003 rs6606822 15:23046848 C 123606 NM_001142275.1 Transcript 3_prime_UTR_variant 2817 - - - - - rs6606822 15:23046848 C 123606 NM_144599.4 Transcript 3_prime_UTR_variant 2996 - - - - - rs6606822 15:23046848 C ENSESTG00000026748 ENSESTT00000067457 Transcript downstream_gene_variant - - - - - - DISTANCE=2231 rs6606822 15:23046848 C ENSESTG00000026748 ENSESTT00000067472 Transcript downstream_gene_variant - - - - - - DISTANCE=2222 rs6606822 15:23046848 C CCDS45190.1 CCDS45190.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1981 rs6606822 15:23046848 C ENSESTG00000026748 ENSESTT00000067379 Transcript downstream_gene_variant - - - - - - DISTANCE=2449 rs6606822 15:23046848 C CCDS10011.1 CCDS10011.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1981 rs6606822 15:23046848 C ENSESTG00000026748 ENSESTT00000067488 Transcript intron_variant - - - - - - rs6606822 15:23046848 C ENSESTG00000026748 ENSESTT00000067359 Transcript downstream_gene_variant - - - - - - DISTANCE=2259 rs6606822 15:23046848 C ENSESTG00000026748 ENSESTT00000067416 Transcript downstream_gene_variant - - - - - - DISTANCE=2240 rs6576410 15:23747008 G - - - intergenic_variant - - - - - - rs4778559 15:23786075 C - - - intergenic_variant - - - - - - rs7497158 15:23786906 G - - - intergenic_variant - - - - - - rs6576491 15:23830104 A - - - intergenic_variant - - - - - - rs8037912 15:23838770 C - - - intergenic_variant - - - - - - rs12899539 15:24057366 G - - - intergenic_variant - - - - - - rs824164 15:24059641 G - - - intergenic_variant - - - - - - rs12440607 15:24209398 C - - - intergenic_variant - - - - - - rs12148888 15:24418349 C ENSESTG00000029347 ENSESTT00000073983 Transcript upstream_gene_variant - - - - - - DISTANCE=3254 rs12148888 15:24418349 C ENSESTG00000029347 ENSESTT00000073872 Transcript intron_variant - - - - - - rs12148888 15:24418349 C ENSESTG00000029418 ENSESTT00000074011 Transcript intron_variant - - - - - - rs12148888 15:24418349 C ENSESTG00000029347 ENSESTT00000073925 Transcript intron_variant - - - - - - rs12148888 15:24418349 C 791115 NR_026647.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3296 rs10873595 15:25071555 C 6638 NM_022807.2 Transcript intron_variant - - - - - - rs10873595 15:25071555 C 6638 NM_022806.2 Transcript intron_variant - - - - - - rs10873595 15:25071555 C ENSESTG00000029793 ENSESTT00000074996 Transcript intron_variant - - - - - - rs10873595 15:25071555 C 6638 NM_022808.2 Transcript intron_variant - - - - - - rs10873595 15:25071555 C ENSESTG00000029793 ENSESTT00000074992 Transcript intron_variant - - - - - - rs10873595 15:25071555 C ENSESTG00000029793 ENSESTT00000074988 Transcript intron_variant - - - - - - rs10873595 15:25071555 C ENSESTG00000029793 ENSESTT00000074951 Transcript intron_variant - - - - - - rs3926484 15:25100719 C ENSESTG00000029793 ENSESTT00000075207 Transcript upstream_gene_variant - - - - - - DISTANCE=968 rs3926484 15:25100719 C ENSESTG00000029793 ENSESTT00000075236 Transcript upstream_gene_variant - - - - - - DISTANCE=968 rs3926484 15:25100719 C ENSESTG00000029793 ENSESTT00000074996 Transcript intron_variant - - - - - - rs3926484 15:25100719 C 6638 NM_022808.2 Transcript intron_variant - - - - - - rs3926484 15:25100719 C ENSESTG00000029793 ENSESTT00000075242 Transcript upstream_gene_variant - - - - - - DISTANCE=968 rs3926484 15:25100719 C ENSESTG00000029793 ENSESTT00000074992 Transcript intron_variant - - - - - - rs3926484 15:25100719 C ENSESTG00000029793 ENSESTT00000074988 Transcript intron_variant - - - - - - rs3926484 15:25100719 C ENSESTG00000029793 ENSESTT00000074951 Transcript intron_variant - - - - - - rs3926484 15:25100719 C 6638 NM_022807.2 Transcript intron_variant - - - - - - rs3926484 15:25100719 C ENSESTG00000029793 ENSESTT00000075250 Transcript upstream_gene_variant - - - - - - DISTANCE=968 rs3926484 15:25100719 C 6638 NM_022806.2 Transcript intron_variant - - - - - - rs3926484 15:25100719 C ENSESTG00000029793 ENSESTT00000075211 Transcript upstream_gene_variant - - - - - - DISTANCE=968 rs3926484 15:25100719 C 6638 NM_022805.2 Transcript upstream_gene_variant - - - - - - DISTANCE=979 rs10782511 15:25415252 C 338433 NR_001291.2 Transcript upstream_gene_variant - - - - - - DISTANCE=618 rs10782511 15:25415252 C 100033440 NR_003295.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4822 rs10782511 15:25415252 C 100033437 NR_003294.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2530 rs7402315 15:25725395 C - - - intergenic_variant - - - - - - rs2930656 15:25834576 G - - - intergenic_variant - - - - - - rs7169798 15:25943476 T 57194 NM_024490.3 Transcript intron_variant - - - - - - rs7169798 15:25943476 T ENSESTG00000029189 ENSESTT00000073485 Transcript upstream_gene_variant - - - - - - DISTANCE=3326 rs7169798 15:25943476 T CCDS32178.1 CCDS32178.1 Transcript intron_variant - - - - - - rs8029834 15:26189351 G ENSESTG00000029010 ENSESTT00000073009 Transcript intron_variant - - - - - - rs8029834 15:26189351 G 100128714 NR_040082.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1473061 15:26226494 G ENSESTG00000029010 ENSESTT00000073009 Transcript intron_variant - - - - - - rs1473061 15:26226494 G 100128714 NR_040082.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7164632 15:26516589 T - - - intergenic_variant - - - - - - rs7165758 15:26523122 C - - - intergenic_variant - - - - - - rs1365584 15:26722648 G - - - intergenic_variant - - - - - - rs4147338 15:26837836 C 2562 NM_021912.4 Transcript intron_variant - - - - - - rs4147338 15:26837836 C CCDS10018.1 CCDS10018.1 Transcript intron_variant - - - - - - rs4147338 15:26837836 C CCDS10019.1 CCDS10019.1 Transcript intron_variant - - - - - - rs4147338 15:26837836 C 2562 NM_001191321.1 Transcript intron_variant - - - - - - rs4147338 15:26837836 C 2562 NM_000814.5 Transcript intron_variant - - - - - - rs4147338 15:26837836 C ENSESTG00000029039 ENSESTT00000073249 Transcript intron_variant - - - - - - rs4147338 15:26837836 C ENSESTG00000029039 ENSESTT00000073230 Transcript intron_variant - - - - - - rs4147338 15:26837836 C 2562 NM_001191320.1 Transcript intron_variant - - - - - - rs4147338 15:26837836 C CCDS53921.1 CCDS53921.1 Transcript intron_variant - - - - - - rs4147338 15:26837836 C CCDS53920.1 CCDS53920.1 Transcript intron_variant - - - - - - rs959936 15:26883895 T 2562 NM_021912.4 Transcript intron_variant - - - - - - rs959936 15:26883895 T CCDS10018.1 CCDS10018.1 Transcript intron_variant - - - - - - rs959936 15:26883895 T CCDS10019.1 CCDS10019.1 Transcript intron_variant - - - - - - rs959936 15:26883895 T ENSESTG00000029039 ENSESTT00000073249 Transcript intron_variant - - - - - - rs959936 15:26883895 T ENSESTG00000029039 ENSESTT00000073230 Transcript intron_variant - - - - - - rs959936 15:26883895 T 2562 NM_000814.5 Transcript intron_variant - - - - - - rs959936 15:26883895 T 2562 NM_001191320.1 Transcript intron_variant - - - - - - rs6576595 15:26950315 G 2562 NM_021912.4 Transcript intron_variant - - - - - - rs6576595 15:26950315 G CCDS10018.1 CCDS10018.1 Transcript intron_variant - - - - - - rs6576595 15:26950315 G CCDS10019.1 CCDS10019.1 Transcript intron_variant - - - - - - rs6576595 15:26950315 G ENSESTG00000029039 ENSESTT00000073249 Transcript intron_variant - - - - - - rs6576595 15:26950315 G ENSESTG00000029039 ENSESTT00000073230 Transcript intron_variant - - - - - - rs6576595 15:26950315 G 2562 NM_000814.5 Transcript intron_variant - - - - - - rs6576595 15:26950315 G 2562 NM_001191320.1 Transcript intron_variant - - - - - - rs12439350 15:27053259 C - - - intergenic_variant - - - - - - rs6420963 15:27091473 A - - - intergenic_variant - - - - - - rs7497927 15:27338598 T CCDS45195.1 CCDS45195.1 Transcript intron_variant - - - - - - rs7497927 15:27338598 T 2567 NM_033223.4 Transcript intron_variant - - - - - - rs6606875 15:27365293 C CCDS45195.1 CCDS45195.1 Transcript intron_variant - - - - - - rs6606875 15:27365293 C 2567 NM_033223.4 Transcript intron_variant - - - - - - rs6606894 15:27514529 A ENSESTG00000035165 ENSESTT00000088865 Transcript upstream_gene_variant - - - - - - DISTANCE=2160 rs6606894 15:27514529 A CCDS45195.1 CCDS45195.1 Transcript intron_variant - - - - - - rs6606894 15:27514529 A ENSESTG00000035165 ENSESTT00000088864 Transcript upstream_gene_variant - - - - - - DISTANCE=2160 rs6606894 15:27514529 A 2567 NM_033223.4 Transcript intron_variant - - - - - - rs6497255 15:28296841 A ENSESTG00000030172 ENSESTT00000075946 Transcript intron_variant - - - - - - rs6497255 15:28296841 A 4948 NM_000275.2 Transcript intron_variant - - - - - - rs6497255 15:28296841 A ENSESTG00000030172 ENSESTT00000075967 Transcript intron_variant - - - - - - rs6497255 15:28296841 A CCDS10020.1 CCDS10020.1 Transcript intron_variant - - - - - - rs6497255 15:28296841 A ENSESTG00000030172 ENSESTT00000075955 Transcript intron_variant - - - - - - rs4778240 15:28338628 C ENSESTG00000030172 ENSESTT00000075946 Transcript intron_variant - - - - - - rs4778240 15:28338628 C 4948 NM_000275.2 Transcript intron_variant - - - - - - rs4778240 15:28338628 C ENSESTG00000030172 ENSESTT00000075967 Transcript intron_variant - - - - - - rs4778240 15:28338628 C ENSESTG00000030172 ENSESTT00000075955 Transcript intron_variant - - - - - - rs4932600 15:28397449 A ENSESTG00000029983 ENSESTT00000075578 Transcript downstream_gene_variant - - - - - - DISTANCE=456 rs4932600 15:28397449 A ENSESTG00000030043 ENSESTT00000075672 Transcript intron_variant - - - - - - rs4932600 15:28397449 A 8924 NM_004667.5 Transcript intron_variant - - - - - - rs4932600 15:28397449 A CCDS10021.1 CCDS10021.1 Transcript intron_variant - - - - - - rs4932600 15:28397449 A ENSESTG00000030043 ENSESTT00000075653 Transcript intron_variant - - - - - - rs1667399 15:28544293 T ENSESTG00000029846 ENSESTT00000075103 Transcript intron_variant - - - - - - rs1667399 15:28544293 T 8924 NM_004667.5 Transcript intron_variant - - - - - - rs1667399 15:28544293 T ENSESTG00000029846 ENSESTT00000075120 Transcript intron_variant - - - - - - rs1667399 15:28544293 T ENSESTG00000029846 ENSESTT00000075114 Transcript intron_variant - - - - - - rs1667399 15:28544293 T ENSESTG00000029846 ENSESTT00000075108 Transcript intron_variant - - - - - - rs1667399 15:28544293 T ENSESTG00000029846 ENSESTT00000075079 Transcript intron_variant - - - - - - rs1667399 15:28544293 T CCDS10021.1 CCDS10021.1 Transcript intron_variant - - - - - - rs1667399 15:28544293 T ENSESTG00000029846 ENSESTT00000075091 Transcript intron_variant - - - - - - rs440947 15:28980714 G ENSESTG00000028617 ENSESTT00000072041 Transcript intron_variant - - - - - - rs440947 15:28980714 G ENSESTG00000028380 ENSESTT00000071361 Transcript upstream_gene_variant - - - - - - DISTANCE=2621 rs440947 15:28980714 G 440253 NR_026589.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2015 rs440947 15:28980714 G ENSESTG00000028617 ENSESTT00000071970 Transcript intron_variant - - - - - - rs440947 15:28980714 G ENSESTG00000028617 ENSESTT00000071981 Transcript intron_variant - - - - - - rs440947 15:28980714 G ENSESTG00000028380 ENSESTT00000071348 Transcript upstream_gene_variant - - - - - - DISTANCE=2454 rs6493161 15:29376032 C ENSESTG00000028505 ENSESTT00000071706 Transcript intron_variant - - - - - - rs6493161 15:29376032 C CCDS45197.1 CCDS45197.1 Transcript intron_variant - - - - - - rs6493161 15:29376032 C CCDS10022.1 CCDS10022.1 Transcript intron_variant - - - - - - rs6493161 15:29376032 C 321 NM_005503.3 Transcript intron_variant - - - - - - rs6493161 15:29376032 C 321 NM_001130414.1 Transcript intron_variant - - - - - - rs4558386 15:29586251 G 23359 NM_015307.1 Transcript intron_variant - - - - - - rs4558386 15:29586251 G ENSESTG00000028569 ENSESTT00000071816 Transcript intron_variant - - - - - - rs4558386 15:29586251 G ENSESTG00000028569 ENSESTT00000071800 Transcript intron_variant - - - - - - rs4558386 15:29586251 G CCDS45198.1 CCDS45198.1 Transcript intron_variant - - - - - - rs12440992 15:30243675 A ENSESTG00000027753 ENSESTT00000069835 Transcript intron_variant - - - - - - rs12594401 15:31194861 T CCDS58344.1 CCDS58344.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2006 rs12594401 15:31194861 T 22909 NM_001146096.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1215 rs12594401 15:31194861 T ENSESTG00000024774 ENSESTT00000062595 Transcript upstream_gene_variant - - - - - - DISTANCE=1215 rs12594401 15:31194861 T 22909 NM_001146094.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1215 rs12594401 15:31194861 T CCDS32186.1 CCDS32186.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2006 rs12594401 15:31194861 T 22909 NM_001146095.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1194 rs12594401 15:31194861 T ENSESTG00000024774 ENSESTT00000062607 Transcript upstream_gene_variant - - - - - - DISTANCE=1257 rs12594401 15:31194861 T 22909 NM_014967.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1215 rs12594401 15:31194861 T ENSESTG00000024799 ENSESTT00000062649 Transcript upstream_gene_variant - - - - - - DISTANCE=3750 rs12594248 15:31194863 A CCDS58344.1 CCDS58344.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2004 rs12594248 15:31194863 A 22909 NM_001146096.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1213 rs12594248 15:31194863 A ENSESTG00000024774 ENSESTT00000062595 Transcript upstream_gene_variant - - - - - - DISTANCE=1213 rs12594248 15:31194863 A 22909 NM_001146094.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1213 rs12594248 15:31194863 A CCDS32186.1 CCDS32186.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2004 rs12594248 15:31194863 A 22909 NM_001146095.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1192 rs12594248 15:31194863 A ENSESTG00000024774 ENSESTT00000062607 Transcript upstream_gene_variant - - - - - - DISTANCE=1255 rs12594248 15:31194863 A 22909 NM_014967.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1213 rs12594248 15:31194863 A ENSESTG00000024799 ENSESTT00000062649 Transcript upstream_gene_variant - - - - - - DISTANCE=3748 rs2959043 15:31329359 C 4308 NM_001252020.1 Transcript intron_variant - - - - - - rs2959043 15:31329359 C CCDS58347.1 CCDS58347.1 Transcript intron_variant - - - - - - rs2959043 15:31329359 C 4308 NM_002420.5 Transcript intron_variant - - - - - - rs2959043 15:31329359 C CCDS10024.2 CCDS10024.2 Transcript intron_variant - - - - - - rs2959043 15:31329359 C 4308 NM_001252024.1 Transcript intron_variant - - - - - - rs2959043 15:31329359 C ENSESTG00000024863 ENSESTT00000062787 Transcript downstream_gene_variant - - - - - - DISTANCE=1186 rs2959043 15:31329359 C CCDS58346.1 CCDS58346.1 Transcript intron_variant - - - - - - rs2911852 15:31329730 A 4308 NM_002420.5 Transcript intron_variant - - - - - - rs2911852 15:31329730 A ENSESTG00000024967 ENSESTT00000063056 Transcript downstream_gene_variant - - - - - - DISTANCE=4693 rs2911852 15:31329730 A 4308 NM_001252024.1 Transcript intron_variant - - - - - - rs2911852 15:31329730 A ENSESTG00000024863 ENSESTT00000062787 Transcript downstream_gene_variant - - - - - - DISTANCE=1557 rs2911852 15:31329730 A 4308 NM_001252020.1 Transcript intron_variant - - - - - - rs2911852 15:31329730 A CCDS58347.1 CCDS58347.1 Transcript intron_variant - - - - - - rs2911852 15:31329730 A CCDS10024.2 CCDS10024.2 Transcript intron_variant - - - - - - rs2911852 15:31329730 A CCDS58346.1 CCDS58346.1 Transcript intron_variant - - - - - - rs4779866 15:31649416 G ENSESTG00000024892 ENSESTT00000062874 Transcript intron_variant - - - - - - rs4779866 15:31649416 G CCDS10025.1 CCDS10025.1 Transcript intron_variant - - - - - - rs4779866 15:31649416 G ENSESTG00000024892 ENSESTT00000062885 Transcript intron_variant - - - - - - rs4779866 15:31649416 G ENSESTG00000024892 ENSESTT00000062854 Transcript intron_variant - - - - - - rs4779866 15:31649416 G ENSESTG00000024892 ENSESTT00000062897 Transcript intron_variant - - - - - - rs4779866 15:31649416 G 51621 NM_015995.2 Transcript intron_variant - - - - - - rs8036705 15:31654857 C ENSESTG00000024892 ENSESTT00000062874 Transcript intron_variant - - - - - - rs8036705 15:31654857 C CCDS10025.1 CCDS10025.1 Transcript intron_variant - - - - - - rs8036705 15:31654857 C ENSESTG00000024892 ENSESTT00000062885 Transcript intron_variant - - - - - - rs8036705 15:31654857 C ENSESTG00000024892 ENSESTT00000062854 Transcript intron_variant - - - - - - rs8036705 15:31654857 C ENSESTG00000024892 ENSESTT00000062907 Transcript upstream_gene_variant - - - - - - DISTANCE=3500 rs8036705 15:31654857 C ENSESTG00000024892 ENSESTT00000062897 Transcript intron_variant - - - - - - rs8036705 15:31654857 C 51621 NM_015995.2 Transcript intron_variant - - - - - - rs7166114 15:31719207 G ENSESTG00000024892 ENSESTT00000062874 Transcript intron_variant - - - - - - rs7166114 15:31719207 G ENSESTG00000024892 ENSESTT00000062917 Transcript intron_variant - - - - - - rs6493713 15:31791139 C CCDS10026.1 CCDS10026.1 Transcript intron_variant - - - - - - rs6493713 15:31791139 C 161725 NM_130901.1 Transcript intron_variant - - - - - - rs1502997 15:32122706 G ENSESTG00000011458 ENSESTT00000028764 Transcript intron_variant - - - - - - rs2048679 15:32211545 C - - - intergenic_variant - - - - - - rs1849700 15:32251294 A - - - intergenic_variant - - - - - - rs9672978 15:32258253 T - - - intergenic_variant - - - - - - rs11071462 15:32281692 A - - - intergenic_variant - - - - - - rs8033155 15:32284471 T - - - intergenic_variant - - - - - - rs1877747 15:32386007 C CCDS10027.1 CCDS10027.1 Transcript intron_variant - - - - - - rs1877747 15:32386007 C 1139 NM_001190455.2 Transcript intron_variant - - - - - - rs1877747 15:32386007 C 1139 NR_046324.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1877747 15:32386007 C CCDS53924.1 CCDS53924.1 Transcript intron_variant - - - - - - rs1877747 15:32386007 C ENSESTG00000011316 ENSESTT00000028428 Transcript intron_variant - - - - - - rs1877747 15:32386007 C 1139 NM_000746.5 Transcript intron_variant - - - - - - rs4779977 15:32391721 A CCDS10027.1 CCDS10027.1 Transcript intron_variant - - - - - - rs4779977 15:32391721 A 1139 NM_001190455.2 Transcript intron_variant - - - - - - rs4779977 15:32391721 A 1139 NR_046324.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4779977 15:32391721 A CCDS53924.1 CCDS53924.1 Transcript intron_variant - - - - - - rs4779977 15:32391721 A ENSESTG00000011316 ENSESTT00000028428 Transcript intron_variant - - - - - - rs4779977 15:32391721 A 1139 NM_000746.5 Transcript intron_variant - - - - - - rs6494224 15:32396480 C CCDS10027.1 CCDS10027.1 Transcript intron_variant - - - - - - rs6494224 15:32396480 C 1139 NM_001190455.2 Transcript intron_variant - - - - - - rs6494224 15:32396480 C 1139 NR_046324.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6494224 15:32396480 C CCDS53924.1 CCDS53924.1 Transcript intron_variant - - - - - - rs6494224 15:32396480 C ENSESTG00000011316 ENSESTT00000028428 Transcript intron_variant - - - - - - rs6494224 15:32396480 C 1139 NM_000746.5 Transcript intron_variant - - - - - - rs1500949 15:32396850 G - ENSR00000405518 RegulatoryFeature regulatory_region_variant - - - - - - rs1500949 15:32396850 G CCDS10027.1 CCDS10027.1 Transcript intron_variant - - - - - - rs1500949 15:32396850 G 1139 NM_001190455.2 Transcript intron_variant - - - - - - rs1500949 15:32396850 G 1139 NR_046324.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1500949 15:32396850 G CCDS53924.1 CCDS53924.1 Transcript intron_variant - - - - - - rs1500949 15:32396850 G ENSESTG00000011316 ENSESTT00000028428 Transcript intron_variant - - - - - - rs1500949 15:32396850 G 1139 NM_000746.5 Transcript intron_variant - - - - - - rs12898347 15:32397597 G CCDS10027.1 CCDS10027.1 Transcript intron_variant - - - - - - rs12898347 15:32397597 G 1139 NM_001190455.2 Transcript intron_variant - - - - - - rs12898347 15:32397597 G 1139 NR_046324.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs12898347 15:32397597 G CCDS53924.1 CCDS53924.1 Transcript intron_variant - - - - - - rs12898347 15:32397597 G ENSESTG00000011316 ENSESTT00000028428 Transcript intron_variant - - - - - - rs12898347 15:32397597 G 1139 NM_000746.5 Transcript intron_variant - - - - - - rs347950 15:33217497 C 342184 NM_001103184.2 Transcript intron_variant - - - - - - rs347950 15:33217497 C ENSESTG00000032974 ENSESTT00000083356 Transcript intron_variant - - - - - - rs347950 15:33217497 C CCDS45209.1 CCDS45209.1 Transcript intron_variant - - - - - - rs347950 15:33217497 C ENSESTG00000032974 ENSESTT00000083360 Transcript intron_variant - - - - - - rs2339261 15:33584789 G - - - intergenic_variant - - - - - - rs1435104 15:33834182 G CCDS58351.1 CCDS58351.1 Transcript intron_variant - - - - - - rs1435104 15:33834182 G 6263 NM_001036.3 Transcript intron_variant - - - - - - rs1435104 15:33834182 G 6263 NM_001243996.1 Transcript intron_variant - - - - - - rs1435104 15:33834182 G CCDS45210.1 CCDS45210.1 Transcript intron_variant - - - - - - rs1369311 15:33859420 G CCDS58351.1 CCDS58351.1 Transcript intron_variant - - - - - - rs1369311 15:33859420 G 6263 NM_001036.3 Transcript intron_variant - - - - - - rs1369311 15:33859420 G 6263 NM_001243996.1 Transcript intron_variant - - - - - - rs1369311 15:33859420 G CCDS45210.1 CCDS45210.1 Transcript intron_variant - - - - - - rs659538 15:33877086 A - ENSR00001451090 RegulatoryFeature regulatory_region_variant - - - - - - rs659538 15:33877086 A CCDS58351.1 CCDS58351.1 Transcript intron_variant - - - - - - rs659538 15:33877086 A 6263 NM_001036.3 Transcript intron_variant - - - - - - rs659538 15:33877086 A 6263 NM_001243996.1 Transcript intron_variant - - - - - - rs659538 15:33877086 A CCDS45210.1 CCDS45210.1 Transcript intron_variant - - - - - - rs9302275 15:33960712 A CCDS58351.1 CCDS58351.1 Transcript intron_variant - - - - - - rs9302275 15:33960712 A 6263 NM_001036.3 Transcript intron_variant - - - - - - rs9302275 15:33960712 A ENSESTG00000011544 ENSESTT00000028936 Transcript intron_variant - - - - - - rs9302275 15:33960712 A 6263 NM_001243996.1 Transcript intron_variant - - - - - - rs9302275 15:33960712 A CCDS45210.1 CCDS45210.1 Transcript intron_variant - - - - - - rs4780172 15:34033560 G CCDS58351.1 CCDS58351.1 Transcript intron_variant - - - - - - rs4780172 15:34033560 G ENSESTG00000011549 ENSESTT00000028943 Transcript intron_variant - - - - - - rs4780172 15:34033560 G 6263 NM_001036.3 Transcript intron_variant - - - - - - rs4780172 15:34033560 G 6263 NM_001243996.1 Transcript intron_variant - - - - - - rs4780172 15:34033560 G CCDS45210.1 CCDS45210.1 Transcript intron_variant - - - - - - rs1560320 15:34045317 G CCDS58351.1 CCDS58351.1 Transcript intron_variant - - - - - - rs1560320 15:34045317 G ENSESTG00000011550 ENSESTT00000028958 Transcript downstream_gene_variant - - - - - - DISTANCE=2900 rs1560320 15:34045317 G ENSESTG00000011556 ENSESTT00000028968 Transcript upstream_gene_variant - - - - - - DISTANCE=3213 rs1560320 15:34045317 G 6263 NM_001036.3 Transcript intron_variant - - - - - - rs1560320 15:34045317 G 6263 NM_001243996.1 Transcript intron_variant - - - - - - rs1560320 15:34045317 G CCDS45210.1 CCDS45210.1 Transcript intron_variant - - - - - - rs4780179 15:34050756 G CCDS58351.1 CCDS58351.1 Transcript intron_variant - - - - - - rs4780179 15:34050756 G ENSESTG00000011556 ENSESTT00000028968 Transcript intron_variant - - - - - - rs4780179 15:34050756 G 6263 NM_001036.3 Transcript intron_variant - - - - - - rs4780179 15:34050756 G 6263 NM_001243996.1 Transcript intron_variant - - - - - - rs4780179 15:34050756 G CCDS45210.1 CCDS45210.1 Transcript intron_variant - - - - - - rs6495703 15:34959185 A - - - intergenic_variant - - - - - - rs674087 15:35063282 C ENSESTG00000026534 ENSESTT00000066802 Transcript intron_variant - - - - - - rs7175459 15:35128319 A ENSESTG00000026544 ENSESTT00000066816 Transcript intron_variant - - - - - - rs2054253 15:35417451 A - - - intergenic_variant - - - - - - rs1444707 15:35486199 G ENSESTG00000026560 ENSESTT00000066851 Transcript intron_variant - - - - - - rs8033041 15:35859191 C ENSESTG00000026195 ENSESTT00000066044 Transcript intron_variant - - - - - - rs8033041 15:35859191 C 100507466 NR_038251.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10152195 15:35961782 C - ENSR00000405962 RegulatoryFeature regulatory_region_variant - - - - - - rs10152195 15:35961782 C ENSESTG00000026195 ENSESTT00000066044 Transcript intron_variant - - - - - - rs10152195 15:35961782 C 100507466 NR_038251.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1846368 15:36001277 G ENSESTG00000026195 ENSESTT00000066044 Transcript intron_variant - - - - - - rs1846368 15:36001277 G 100507466 NR_038251.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2683092 15:36153061 T ENSESTG00000026195 ENSESTT00000066044 Transcript downstream_gene_variant - - - - - - DISTANCE=2583 rs2683092 15:36153061 T 100507466 NR_038251.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1859 rs2340000 15:36301630 A - - - intergenic_variant - - - - - - rs4924040 15:36307019 G - - - intergenic_variant - - - - - - rs12708538 15:36324643 C - ENSR00000650389 RegulatoryFeature regulatory_region_variant - - - - - - rs12708538 15:36324643 C - - - intergenic_variant - - - - - - rs789904 15:36364397 T - - - intergenic_variant - - - - - - rs789867 15:36372498 T - - - intergenic_variant - - - - - - rs4315299 15:36662514 A - - - intergenic_variant - - - - - - rs4924063 15:36677305 A - - - intergenic_variant - - - - - - rs1996646 15:37505283 A - - - intergenic_variant - - - - - - rs12102218 15:37587939 C - - - intergenic_variant - - - - - - rs1840903 15:37746283 G - - - intergenic_variant - - - - - - rs2959338 15:38254326 G - - - intergenic_variant - - - - - - rs7173790 15:38502778 A - - - intergenic_variant - - - - - - rs6495978 15:38846031 G ENSESTG00000003294 ENSESTT00000008216 Transcript intron_variant - - - - - - rs6495978 15:38846031 G 10125 NM_001128602.1 Transcript intron_variant - - - - - - rs6495978 15:38846031 G CCDS45221.1 CCDS45221.1 Transcript intron_variant - - - - - - rs6495978 15:38846031 G CCDS45222.1 CCDS45222.1 Transcript intron_variant - - - - - - rs6495978 15:38846031 G 10125 NM_005739.3 Transcript intron_variant - - - - - - rs6495978 15:38846031 G ENSESTG00000003294 ENSESTT00000008236 Transcript intron_variant - - - - - - rs6495978 15:38846031 G ENSESTG00000003294 ENSESTT00000008224 Transcript intron_variant - - - - - - rs6495978 15:38846031 G ENSESTG00000003294 ENSESTT00000008221 Transcript intron_variant - - - - - - rs6495978 15:38846031 G ENSESTG00000003294 ENSESTT00000008219 Transcript intron_variant - - - - - - rs6495978 15:38846031 G ENSESTG00000003294 ENSESTT00000008238 Transcript intron_variant - - - - - - rs2912373 15:39047387 A ENSESTG00000032062 ENSESTT00000080901 Transcript downstream_gene_variant - - - - - - DISTANCE=1368 rs2912373 15:39047387 A ENSESTG00000032062 ENSESTT00000080894 Transcript downstream_gene_variant - - - - - - DISTANCE=1704 rs2958301 15:39071736 G - - - intergenic_variant - - - - - - rs2411227 15:39265986 T ENSESTG00000032037 ENSESTT00000080864 Transcript downstream_gene_variant - - - - - - DISTANCE=364 rs2411227 15:39265986 T ENSESTG00000032037 ENSESTT00000080855 Transcript intron_variant - - - - - - rs2411227 15:39265986 T ENSESTG00000032037 ENSESTT00000080849 Transcript intron_variant - - - - - - rs275219 15:39412685 G - - - intergenic_variant - - - - - - rs504409 15:39417950 A - - - intergenic_variant - - - - - - rs4569242 15:39709600 T ENSESTG00000032020 ENSESTT00000080798 Transcript intron_variant - - - - - - rs4569242 15:39709600 T ENSESTG00000032024 ENSESTT00000080805 Transcript intron_variant - - - - - - rs8039889 15:39740625 T - ENSR00001451501 RegulatoryFeature regulatory_region_variant - - - - - - rs8039889 15:39740625 T - - - intergenic_variant - - - - - - rs2411294 15:39743304 G - - - intergenic_variant - - - - - - rs922461 15:39784310 T - ENSR00000236596 RegulatoryFeature regulatory_region_variant - - - - - - rs922461 15:39784310 T - - - intergenic_variant - - - - - - rs746059 15:39788977 A - - - intergenic_variant - - - - - - rs899284 15:39789743 C - - - intergenic_variant - - - - - - rs1159996 15:39810417 G ENSESTG00000032011 ENSESTT00000080788 Transcript upstream_gene_variant - - - - - - DISTANCE=4340 rs1159996 15:39810417 G ENSESTG00000032011 ENSESTT00000080780 Transcript intron_variant - - - - - - rs1159996 15:39810417 G ENSESTG00000032011 ENSESTT00000080772 Transcript intron_variant - - - - - - rs2412457 15:40291140 T ENSESTG00000024423 ENSESTT00000062550 Transcript intron_variant - - - - - - rs2412457 15:40291140 T CCDS42016.1 CCDS42016.1 Transcript intron_variant - - - - - - rs2412457 15:40291140 T ENSESTG00000024423 ENSESTT00000062616 Transcript upstream_gene_variant - - - - - - DISTANCE=3452 rs2412457 15:40291140 T 440275 NM_001013703.2 Transcript intron_variant - - - - - - rs2412457 15:40291140 T ENSESTG00000024423 ENSESTT00000062486 Transcript intron_variant - - - - - - rs2412457 15:40291140 T ENSESTG00000024423 ENSESTT00000062594 Transcript upstream_gene_variant - - - - - - DISTANCE=3452 rs2412457 15:40291140 T ENSESTG00000024423 ENSESTT00000062589 Transcript upstream_gene_variant - - - - - - DISTANCE=3452 rs2412457 15:40291140 T ENSESTG00000024423 ENSESTT00000062515 Transcript intron_variant - - - - - - rs2412457 15:40291140 T ENSESTG00000024423 ENSESTT00000062560 Transcript intron_variant - - - - - - rs2412457 15:40291140 T ENSESTG00000024423 ENSESTT00000062577 Transcript intron_variant - - - - - - rs7181948 15:40434558 G - - - intergenic_variant - - - - - - rs6492972 15:41252705 G 79094 NM_001142776.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3988 rs6492972 15:41252705 G ENSESTG00000019821 ENSESTT00000049705 Transcript downstream_gene_variant - - - - - - DISTANCE=4840 rs6492972 15:41252705 G 79094 NM_024111.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3988 rs6492972 15:41252705 G CCDS10070.2 CCDS10070.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4733 rs6492972 15:41252705 G CCDS45233.1 CCDS45233.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4733 rs7174630 15:41716604 G - ENSR00000406807 RegulatoryFeature regulatory_region_variant - - - - - - rs7174630 15:41716604 G CCDS32200.2 CCDS32200.2 Transcript intron_variant - - - - - - rs7174630 15:41716604 G 23168 NM_015138.4 Transcript intron_variant - - - - - - rs1200347 15:41821011 C ENSESTG00000007126 ENSESTT00000018025 Transcript intron_variant - - - - - - rs1200347 15:41821011 C ENSESTG00000007126 ENSESTT00000018022 Transcript intron_variant - - - - - - rs1200347 15:41821011 C 26015 NM_015540.2 Transcript intron_variant - - - - - - rs1200347 15:41821011 C CCDS10079.1 CCDS10079.1 Transcript intron_variant - - - - - - rs4344712 15:41854277 C - ENSR00000020643 RegulatoryFeature regulatory_region_variant - - - - - - rs4344712 15:41854277 C ENSESTG00000006522 ENSESTT00000016488 Transcript intron_variant - - - - - - rs4344712 15:41854277 C CCDS10080.1 CCDS10080.1 Transcript intron_variant - - - - - - rs4344712 15:41854277 C 7301 NM_006293.3 Transcript intron_variant - - - - - - rs1200338 15:41854518 A ENSESTG00000006522 ENSESTT00000016488 Transcript intron_variant - - - - - - rs1200338 15:41854518 A CCDS10080.1 CCDS10080.1 Transcript intron_variant - - - - - - rs1200338 15:41854518 A 7301 NM_006293.3 Transcript intron_variant - - - - - - rs2588324 15:41867003 G ENSESTG00000006522 ENSESTT00000016488 Transcript intron_variant - - - - - - rs2588324 15:41867003 G CCDS10080.1 CCDS10080.1 Transcript intron_variant - - - - - - rs2588324 15:41867003 G ENSESTG00000006522 ENSESTT00000016490 Transcript intron_variant - - - - - - rs2588324 15:41867003 G 7301 NM_006293.3 Transcript intron_variant - - - - - - rs2588327 15:41880659 C - ENSR00000406831 RegulatoryFeature regulatory_region_variant - - - - - - rs2588327 15:41880659 C - - - intergenic_variant - - - - - - rs2555558 15:42215157 C 30844 NM_139265.3 Transcript intron_variant - - - - - - rs2555558 15:42215157 C CCDS10081.1 CCDS10081.1 Transcript intron_variant - - - - - - rs2555558 15:42215157 C ENSESTG00000007105 ENSESTT00000017991 Transcript intron_variant - - - - - - rs776700 15:42350362 G - ENSR00001451709 RegulatoryFeature regulatory_region_variant - - - - - - rs776700 15:42350362 G - - - intergenic_variant - - - - - - rs8031245 15:43283346 C ENSESTG00000006713 ENSESTT00000017114 Transcript intron_variant - - - - - - rs8031245 15:43283346 C ENSESTG00000006713 ENSESTT00000017116 Transcript intron_variant - - - - - - rs8031245 15:43283346 C ENSESTG00000006713 ENSESTT00000017111 Transcript intron_variant - - - - - - rs8031245 15:43283346 C 197131 NM_174916.2 Transcript intron_variant - - - - - - rs8031245 15:43283346 C CCDS10091.1 CCDS10091.1 Transcript intron_variant - - - - - - rs8031245 15:43283346 C ENSESTG00000006713 ENSESTT00000017113 Transcript intron_variant - - - - - - rs4924708 15:43449276 T ENSESTG00000006481 ENSESTT00000016335 Transcript intron_variant - - - - - - rs4924708 15:43449276 T CCDS32210.1 CCDS32210.1 Transcript intron_variant - - - - - - rs4924708 15:43449276 T ENSESTG00000006481 ENSESTT00000016332 Transcript intron_variant - - - - - - rs4924708 15:43449276 T ENSESTG00000006481 ENSESTT00000016342 Transcript intron_variant - - - - - - rs4924708 15:43449276 T ENSESTG00000006481 ENSESTT00000016339 Transcript intron_variant - - - - - - rs4924708 15:43449276 T 80021 NM_024956.3 Transcript intron_variant - - - - - - rs4924708 15:43449276 T ENSESTG00000006481 ENSESTT00000016338 Transcript intron_variant - - - - - - rs2615282 15:44542445 G - - - intergenic_variant - - - - - - rs175224 15:45320019 G 6652 NM_003104.5 Transcript intron_variant - - - - - - rs175224 15:45320019 G 6652 NR_034039.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs175224 15:45320019 G CCDS10116.1 CCDS10116.1 Transcript intron_variant - - - - - - rs2433226 15:45423733 G 53905 NM_017434.3 Transcript 5_prime_UTR_variant 170 - - - - - rs2433226 15:45423733 G ENSESTG00000005693 ENSESTT00000014447 Transcript upstream_gene_variant - - - - - - DISTANCE=1658 rs2433226 15:45423733 G CCDS32221.1 CCDS32221.1 Transcript upstream_gene_variant - - - - - - DISTANCE=432 rs2433226 15:45423733 G 53905 NM_175940.1 Transcript intron_variant - - - - - - rs2433226 15:45423733 G ENSESTG00000005693 ENSESTT00000014443 Transcript upstream_gene_variant - - - - - - DISTANCE=1658 rs2433226 15:45423733 G 90527 NM_144565.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1676 rs1648294 15:45524453 A - - - intergenic_variant - - - - - - rs4774554 15:45565563 C CCDS10121.1 CCDS10121.1 Transcript intron_variant - - - - - - rs4774554 15:45565563 C 9153 NM_004212.3 Transcript intron_variant - - - - - - rs1626641 15:45603141 G - ENSR00001022872 RegulatoryFeature regulatory_region_variant - - - - - - rs1626641 15:45603141 G - - - intergenic_variant - - - - - - rs2670814 15:45918994 T ENSESTG00000034396 ENSESTT00000087005 Transcript upstream_gene_variant - - - - - - DISTANCE=4788 rs9806540 15:46536531 G - - - intergenic_variant - - - - - - rs1385083 15:46710605 C - - - intergenic_variant - - - - - - rs6493237 15:47097215 C - - - intergenic_variant - - - - - - rs4288943 15:47140179 G - - - intergenic_variant - - - - - - rs1588622 15:47260773 A - - - intergenic_variant - - - - - - rs2675350 15:47480638 A ENSESTG00000021562 ENSESTT00000054101 Transcript intron_variant - - - - - - rs2675350 15:47480638 A 80031 NM_001198999.1 Transcript intron_variant - - - - - - rs2645328 15:47648392 A ENSESTG00000021601 ENSESTT00000054217 Transcript downstream_gene_variant - - - - - - DISTANCE=3601 rs2645328 15:47648392 A ENSESTG00000021562 ENSESTT00000054101 Transcript intron_variant - - - - - - rs2645328 15:47648392 A 80031 NM_001198999.1 Transcript intron_variant - - - - - - rs281319 15:47770215 C ENSESTG00000021562 ENSESTT00000054120 Transcript intron_variant - - - - - - rs281319 15:47770215 C ENSESTG00000021562 ENSESTT00000054101 Transcript intron_variant - - - - - - rs281319 15:47770215 C ENSESTG00000021562 ENSESTT00000054144 Transcript intron_variant - - - - - - rs281319 15:47770215 C 80031 NM_001198999.1 Transcript intron_variant - - - - - - rs281319 15:47770215 C ENSESTG00000021562 ENSESTT00000054163 Transcript intron_variant - - - - - - rs12594456 15:47967388 T ENSESTG00000021562 ENSESTT00000054120 Transcript intron_variant - - - - - - rs12594456 15:47967388 T ENSESTG00000021562 ENSESTT00000054101 Transcript intron_variant - - - - - - rs12594456 15:47967388 T ENSESTG00000021562 ENSESTT00000054144 Transcript intron_variant - - - - - - rs12594456 15:47967388 T 80031 NM_001198999.1 Transcript intron_variant - - - - - - rs520201 15:48183752 G - - - intergenic_variant - - - - - - rs2433355 15:48415261 T ENSESTG00000015902 ENSESTT00000039922 Transcript intron_variant - - - - - - rs2433355 15:48415261 T 283652 NM_205850.2 Transcript intron_variant - - - - - - rs2433355 15:48415261 T CCDS10128.1 CCDS10128.1 Transcript intron_variant - - - - - - rs965828 15:48428591 A ENSESTG00000015902 ENSESTT00000039922 Transcript intron_variant - - - - - - rs965828 15:48428591 A 283652 NM_205850.2 Transcript intron_variant - - - - - - rs965828 15:48428591 A ENSESTG00000015902 ENSESTT00000039935 Transcript 5_prime_UTR_variant 740 - - - - - rs965828 15:48428591 A CCDS10128.1 CCDS10128.1 Transcript intron_variant - - - - - - rs965828 15:48428591 A 50804 NM_016132.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3038 rs2470103 15:48443699 C ENSESTG00000016283 ENSESTT00000040928 Transcript missense_variant 1557 1277 426 Q/R cAa/cGa - rs2470103 15:48443699 C ENSESTG00000016283 ENSESTT00000040944 Transcript upstream_gene_variant - - - - - - DISTANCE=328 rs2470103 15:48443699 C CCDS32230.1 CCDS32230.1 Transcript missense_variant 1277 1277 426 Q/R cAa/cGa - PolyPhen=benign;SIFT=tolerated rs2470103 15:48443699 C 50804 NM_016132.3 Transcript missense_variant 1401 1277 426 Q/R cAa/cGa - PolyPhen=benign;SIFT=tolerated rs2927579 15:49029516 A 22995 NM_014985.3 Transcript downstream_gene_variant - - - - - - DISTANCE=619 rs2927579 15:49029516 A 22995 NM_001194998.1 Transcript downstream_gene_variant - - - - - - DISTANCE=619 rs2927579 15:49029516 A CCDS42033.1 CCDS42033.1 Transcript downstream_gene_variant - - - - - - DISTANCE=930 rs2927579 15:49029516 A CCDS58361.1 CCDS58361.1 Transcript downstream_gene_variant - - - - - - DISTANCE=930 rs1469294 15:49080211 C 22995 NM_014985.3 Transcript intron_variant - - - - - - rs1469294 15:49080211 C 22995 NM_001194998.1 Transcript intron_variant - - - - - - rs1469294 15:49080211 C CCDS42033.1 CCDS42033.1 Transcript intron_variant - - - - - - rs1469294 15:49080211 C CCDS58361.1 CCDS58361.1 Transcript intron_variant - - - - - - rs2413919 15:49212193 T ENSESTG00000024517 ENSESTT00000061981 Transcript intron_variant - - - - - - rs2413919 15:49212193 T CCDS10130.1 CCDS10130.1 Transcript intron_variant - - - - - - rs2413919 15:49212193 T 399694 NM_203349.3 Transcript intron_variant - - - - - - rs2413919 15:49212193 T ENSESTG00000024871 ENSESTT00000062864 Transcript intron_variant - - - - - - rs8025455 15:49796655 T 196951 NM_152647.2 Transcript intron_variant - - - - - - rs8025455 15:49796655 T ENSESTG00000024718 ENSESTT00000062459 Transcript intron_variant - - - - - - rs8025455 15:49796655 T CCDS32237.1 CCDS32237.1 Transcript intron_variant - - - - - - rs8023535 15:49866525 T 196951 NM_152647.2 Transcript intron_variant - - - - - - rs8023535 15:49866525 T CCDS32237.1 CCDS32237.1 Transcript intron_variant - - - - - - rs4774549 15:50152583 T - ENSR00001452104 RegulatoryFeature regulatory_region_variant - - - - - - rs4774549 15:50152583 T ENSESTG00000003332 ENSESTT00000008316 Transcript downstream_gene_variant - - - - - - DISTANCE=42 rs4774549 15:50152583 T CCDS32238.1 CCDS32238.1 Transcript synonymous_variant 3387 3387 1129 G ggC/ggA - rs4774549 15:50152583 T 79895 NM_024837.2 Transcript synonymous_variant 3529 3387 1129 G ggC/ggA - rs2617239 15:50612940 T 2553 NM_016654.4 Transcript intron_variant - - - - - - rs2617239 15:50612940 T 2553 NM_002041.4 Transcript intron_variant - - - - - - rs2617239 15:50612940 T ENSESTG00000003399 ENSESTT00000008510 Transcript intron_variant - - - - - - rs2617239 15:50612940 T 2553 NM_005254.5 Transcript intron_variant - - - - - - rs2617239 15:50612940 T ENSESTG00000003399 ENSESTT00000008503 Transcript intron_variant - - - - - - rs2617239 15:50612940 T 2553 NM_016655.4 Transcript intron_variant - - - - - - rs2617239 15:50612940 T ENSESTG00000003399 ENSESTT00000008513 Transcript intron_variant - - - - - - rs2617239 15:50612940 T 2553 NM_181427.3 Transcript intron_variant - - - - - - rs8034732 15:51300049 C 23431 NM_007347.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1952 rs8034732 15:51300049 C ENSESTG00000011970 ENSESTT00000030018 Transcript downstream_gene_variant - - - - - - DISTANCE=4910 rs8034732 15:51300049 C 23431 NM_001252127.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1952 rs2090356 15:51817162 G CCDS10141.1 CCDS10141.1 Transcript intron_variant - - - - - - rs2090356 15:51817162 G 23312 NM_001174117.1 Transcript intron_variant - - - - - - rs2090356 15:51817162 G CCDS53946.1 CCDS53946.1 Transcript intron_variant - - - - - - rs2090356 15:51817162 G CCDS53945.1 CCDS53945.1 Transcript intron_variant - - - - - - rs2090356 15:51817162 G 23312 NM_001174116.1 Transcript intron_variant - - - - - - rs2090356 15:51817162 G 23312 NM_015263.3 Transcript intron_variant - - - - - - rs1902599 15:51915312 A - ENSR00000237159 RegulatoryFeature regulatory_region_variant - - - - - - rs1902599 15:51915312 A ENSESTG00000019257 ENSESTT00000048398 Transcript upstream_gene_variant - - - - - - DISTANCE=282 rs1902599 15:51915312 A 23312 NM_001174117.1 Transcript upstream_gene_variant - - - - - - DISTANCE=345 rs1902599 15:51915312 A ENSESTG00000019257 ENSESTT00000048386 Transcript upstream_gene_variant - - - - - - DISTANCE=282 rs1902599 15:51915312 A 23312 NM_015263.3 Transcript upstream_gene_variant - - - - - - DISTANCE=345 rs1902599 15:51915312 A CCDS10141.1 CCDS10141.1 Transcript upstream_gene_variant - - - - - - DISTANCE=570 rs1902599 15:51915312 A CCDS53946.1 CCDS53946.1 Transcript upstream_gene_variant - - - - - - DISTANCE=570 rs1902599 15:51915312 A 23312 NM_001174116.1 Transcript upstream_gene_variant - - - - - - DISTANCE=345 rs1902599 15:51915312 A CCDS53945.1 CCDS53945.1 Transcript upstream_gene_variant - - - - - - DISTANCE=570 rs1993455 15:51926296 C - - - intergenic_variant - - - - - - rs2622771 15:51969347 T - ENSR00001452215 RegulatoryFeature regulatory_region_variant - - - - - - rs2622771 15:51969347 T 29106 NM_001165257.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4203 rs2622771 15:51969347 T CCDS10142.1 CCDS10142.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4606 rs2622771 15:51969347 T 29106 NM_013243.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4203 rs2622771 15:51969347 T ENSESTG00000018480 ENSESTT00000046600 Transcript upstream_gene_variant - - - - - - DISTANCE=4287 rs897582 15:51972552 T 29106 NM_001165257.1 Transcript upstream_gene_variant - - - - - - DISTANCE=998 rs897582 15:51972552 T CCDS10142.1 CCDS10142.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1401 rs897582 15:51972552 T 29106 NM_013243.3 Transcript upstream_gene_variant - - - - - - DISTANCE=998 rs897582 15:51972552 T ENSESTG00000018480 ENSESTT00000046600 Transcript upstream_gene_variant - - - - - - DISTANCE=1082 rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047083 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047121 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047036 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047105 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047101 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047119 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047077 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047026 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047040 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047056 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047042 Transcript intron_variant - - - - - - rs2921956 15:52331131 G 5597 NM_002748.3 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047022 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047061 Transcript intron_variant - - - - - - rs2921956 15:52331131 G ENSESTG00000018663 ENSESTT00000047030 Transcript intron_variant - - - - - - rs6493550 15:52537044 C CCDS42036.1 CCDS42036.1 Transcript intron_variant - - - - - - rs6493550 15:52537044 C 55930 NM_018728.3 Transcript intron_variant - - - - - - rs6493550 15:52537044 C ENSESTG00000019011 ENSESTT00000047847 Transcript downstream_gene_variant - - - - - - DISTANCE=3909 rs4776035 15:52587364 G - ENSR00000408066 RegulatoryFeature regulatory_region_variant - - - - - - rs4776035 15:52587364 G CCDS42036.1 CCDS42036.1 Transcript intron_variant - - - - - - rs4776035 15:52587364 G 55930 NM_018728.3 Transcript intron_variant - - - - - - rs4776035 15:52587364 G ENSESTG00000018965 ENSESTT00000047783 Transcript intron_variant - - - - - - rs11856560 15:52875886 C ENSESTG00000034111 ENSESTT00000086242 Transcript intron_variant - - - - - - rs11856560 15:52875886 C CCDS45263.1 CCDS45263.1 Transcript intron_variant - - - - - - rs11856560 15:52875886 C ENSESTG00000034156 ENSESTT00000086345 Transcript downstream_gene_variant - - - - - - DISTANCE=3245 rs11856560 15:52875886 C ENSESTG00000034156 ENSESTT00000086350 Transcript intron_variant - - - - - - rs11856560 15:52875886 C ENSESTG00000034156 ENSESTT00000086343 Transcript downstream_gene_variant - - - - - - DISTANCE=1069 rs11856560 15:52875886 C ENSESTG00000034156 ENSESTT00000086341 Transcript intron_variant - - - - - - rs11856560 15:52875886 C 56204 NM_019600.2 Transcript intron_variant - - - - - - rs11070903 15:52876014 T ENSESTG00000034111 ENSESTT00000086242 Transcript intron_variant - - - - - - rs11070903 15:52876014 T CCDS45263.1 CCDS45263.1 Transcript intron_variant - - - - - - rs11070903 15:52876014 T ENSESTG00000034156 ENSESTT00000086345 Transcript downstream_gene_variant - - - - - - DISTANCE=3117 rs11070903 15:52876014 T ENSESTG00000034156 ENSESTT00000086350 Transcript intron_variant - - - - - - rs11070903 15:52876014 T ENSESTG00000034156 ENSESTT00000086343 Transcript downstream_gene_variant - - - - - - DISTANCE=941 rs11070903 15:52876014 T ENSESTG00000034156 ENSESTT00000086341 Transcript intron_variant - - - - - - rs11070903 15:52876014 T 56204 NM_019600.2 Transcript intron_variant - - - - - - rs561749 15:53508087 A - - - intergenic_variant - - - - - - rs1983385 15:53530590 T - - - intergenic_variant - - - - - - rs7172366 15:53925904 A ENSESTG00000024092 ENSESTT00000060893 Transcript intron_variant - - - - - - rs7172366 15:53925904 A CCDS10151.1 CCDS10151.1 Transcript intron_variant - - - - - - rs7172366 15:53925904 A 256764 NM_182758.2 Transcript intron_variant - - - - - - rs11852907 15:54503767 G ENSESTG00000023712 ENSESTT00000059846 Transcript intron_variant - - - - - - rs11852907 15:54503767 G CCDS45264.1 CCDS45264.1 Transcript intron_variant - - - - - - rs11852907 15:54503767 G 440279 NM_001080534.1 Transcript intron_variant - - - - - - rs10152151 15:54535306 G ENSESTG00000023712 ENSESTT00000059846 Transcript intron_variant - - - - - - rs10152151 15:54535306 G CCDS45264.1 CCDS45264.1 Transcript intron_variant - - - - - - rs10152151 15:54535306 G 440279 NM_001080534.1 Transcript intron_variant - - - - - - rs4633657 15:54569974 A CCDS45264.1 CCDS45264.1 Transcript intron_variant - - - - - - rs4633657 15:54569974 A ENSESTG00000023712 ENSESTT00000060002 Transcript intron_variant - - - - - - rs4633657 15:54569974 A 440279 NM_001080534.1 Transcript intron_variant - - - - - - rs2553219 15:54869044 A - ENSR00000650648 RegulatoryFeature regulatory_region_variant - - - - - - rs2553219 15:54869044 A CCDS45264.1 CCDS45264.1 Transcript intron_variant - - - - - - rs2553219 15:54869044 A ENSESTG00000032989 ENSESTT00000083467 Transcript intron_variant - - - - - - rs2553219 15:54869044 A ENSESTG00000032989 ENSESTT00000083469 Transcript intron_variant - - - - - - rs2553219 15:54869044 A 440279 NM_001080534.1 Transcript intron_variant - - - - - - rs2414333 15:54927903 T - - - intergenic_variant - - - - - - rs8036229 15:54935200 C - - - intergenic_variant - - - - - - rs2414352 15:54961214 G - - - intergenic_variant - - - - - - rs4307901 15:55003913 A - - - intergenic_variant - - - - - - rs9919980 15:55004753 C - - - intergenic_variant - - - - - - rs2414368 15:55006797 G - - - intergenic_variant - - - - - - rs4509959 15:55008258 G - - - intergenic_variant - - - - - - rs2651729 15:55083469 A - - - intergenic_variant - - - - - - rs1690362 15:55310692 A - - - intergenic_variant - - - - - - rs2697384 15:55365010 T ENSESTG00000033029 ENSESTT00000083492 Transcript intron_variant - - - - - - rs4774207 15:55501766 G 5873 NM_183235.2 Transcript intron_variant - - - - - - rs4774207 15:55501766 G 5873 NM_183234.2 Transcript intron_variant - - - - - - rs4774207 15:55501766 G ENSESTG00000033163 ENSESTT00000083837 Transcript intron_variant - - - - - - rs4774207 15:55501766 G 5873 NM_004580.4 Transcript intron_variant - - - - - - rs4774207 15:55501766 G CCDS10153.1 CCDS10153.1 Transcript intron_variant - - - - - - rs4774207 15:55501766 G ENSESTG00000033163 ENSESTT00000083854 Transcript intron_variant - - - - - - rs4774207 15:55501766 G 5873 NM_183236.2 Transcript intron_variant - - - - - - rs2414439 15:56075757 G - - - intergenic_variant - - - - - - rs11629860 15:56078516 G - - - intergenic_variant - - - - - - rs1991405 15:56093849 G - - - intergenic_variant - - - - - - rs8034639 15:56103684 C - - - intergenic_variant - - - - - - rs1991404 15:56154366 A ENSESTG00000005851 ENSESTT00000014867 Transcript intron_variant - - - - - - rs1991404 15:56154366 A ENSESTG00000005851 ENSESTT00000014858 Transcript intron_variant - - - - - - rs1991404 15:56154366 A ENSESTG00000005851 ENSESTT00000014881 Transcript intron_variant - - - - - - rs1991404 15:56154366 A 4734 NM_006154.2 Transcript intron_variant - - - - - - rs1991404 15:56154366 A 4734 NM_198400.2 Transcript intron_variant - - - - - - rs1991404 15:56154366 A CCDS10156.1 CCDS10156.1 Transcript intron_variant - - - - - - rs1991404 15:56154366 A ENSESTG00000005851 ENSESTT00000014877 Transcript intron_variant - - - - - - rs1991404 15:56154366 A CCDS45265.1 CCDS45265.1 Transcript intron_variant - - - - - - rs1991404 15:56154366 A ENSESTG00000005851 ENSESTT00000014861 Transcript intron_variant - - - - - - rs4480735 15:56172220 G ENSESTG00000005851 ENSESTT00000014867 Transcript intron_variant - - - - - - rs4480735 15:56172220 G ENSESTG00000005851 ENSESTT00000014858 Transcript intron_variant - - - - - - rs4480735 15:56172220 G ENSESTG00000005851 ENSESTT00000014881 Transcript intron_variant - - - - - - rs4480735 15:56172220 G 4734 NM_006154.2 Transcript intron_variant - - - - - - rs4480735 15:56172220 G 4734 NM_198400.2 Transcript intron_variant - - - - - - rs4480735 15:56172220 G CCDS10156.1 CCDS10156.1 Transcript intron_variant - - - - - - rs4480735 15:56172220 G ENSESTG00000005851 ENSESTT00000014877 Transcript intron_variant - - - - - - rs4480735 15:56172220 G CCDS45265.1 CCDS45265.1 Transcript intron_variant - - - - - - rs4480735 15:56172220 G ENSESTG00000005851 ENSESTT00000014861 Transcript intron_variant - - - - - - rs62046380 15:56299364 A - ENSR00000408347 RegulatoryFeature regulatory_region_variant - - - - - - rs62046380 15:56299364 A - - - intergenic_variant - - - - - - rs7170589 15:56386577 G 64864 NM_022841.5 Transcript missense_variant 3349 3349 1117 N/H Aat/Cat - PolyPhen=benign;SIFT=tolerated rs1031078 15:56394806 T 64864 NM_022841.5 Transcript intron_variant - - - - - - rs1031078 15:56394806 T ENSESTG00000005840 ENSESTT00000014816 Transcript downstream_gene_variant - - - - - - DISTANCE=965 rs2682058 15:56556619 C ENSESTG00000005800 ENSESTT00000014683 Transcript intron_variant - - - - - - rs2247095 15:56611505 A ENSESTG00000005800 ENSESTT00000014683 Transcript intron_variant - - - - - - rs1582755 15:56669211 C ENSESTG00000005800 ENSESTT00000014723 Transcript intron_variant - - - - - - rs1582755 15:56669211 C ENSESTG00000005800 ENSESTT00000014698 Transcript intron_variant - - - - - - rs1582755 15:56669211 C 374618 NM_198524.1 Transcript intron_variant - - - - - - rs1582755 15:56669211 C CCDS10157.1 CCDS10157.1 Transcript intron_variant - - - - - - rs1582755 15:56669211 C ENSESTG00000005800 ENSESTT00000014717 Transcript intron_variant - - - - - - rs1582755 15:56669211 C ENSESTG00000005800 ENSESTT00000014710 Transcript intron_variant - - - - - - rs1582755 15:56669211 C ENSESTG00000005800 ENSESTT00000014683 Transcript intron_variant - - - - - - rs795799 15:56712734 G 374618 NM_198524.1 Transcript intron_variant - - - - - - rs795799 15:56712734 G ENSESTG00000005810 ENSESTT00000014734 Transcript intron_variant - - - - - - rs795799 15:56712734 G CCDS10157.1 CCDS10157.1 Transcript intron_variant - - - - - - rs795783 15:56716863 T ENSESTG00000005836 ENSESTT00000014787 Transcript downstream_gene_variant - - - - - - DISTANCE=4138 rs795783 15:56716863 T 55329 NM_018365.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4066 rs795783 15:56716863 T 374618 NM_198524.1 Transcript intron_variant - - - - - - rs795783 15:56716863 T ENSESTG00000005810 ENSESTT00000014743 Transcript upstream_gene_variant - - - - - - DISTANCE=3013 rs795783 15:56716863 T ENSESTG00000005810 ENSESTT00000014734 Transcript intron_variant - - - - - - rs795783 15:56716863 T CCDS10158.1 CCDS10158.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4436 rs795783 15:56716863 T CCDS10157.1 CCDS10157.1 Transcript intron_variant - - - - - - rs6493883 15:57016626 G ENSESTG00000000112 ENSESTT00000000294 Transcript intron_variant - - - - - - rs6493883 15:57016626 G ENSESTG00000000112 ENSESTT00000000295 Transcript intron_variant - - - - - - rs6493883 15:57016626 G ENSESTG00000000112 ENSESTT00000000298 Transcript intron_variant - - - - - - rs6493883 15:57016626 G 54816 NM_017661.2 Transcript intron_variant - - - - - - rs6493883 15:57016626 G ENSESTG00000000112 ENSESTT00000000293 Transcript intron_variant - - - - - - rs6493883 15:57016626 G 54816 NM_001002843.1 Transcript intron_variant - - - - - - rs6493883 15:57016626 G 54816 NM_001002844.1 Transcript intron_variant - - - - - - rs8024848 15:57021195 T ENSESTG00000000112 ENSESTT00000000294 Transcript intron_variant - - - - - - rs8024848 15:57021195 T ENSESTG00000000112 ENSESTT00000000295 Transcript intron_variant - - - - - - rs8024848 15:57021195 T ENSESTG00000000112 ENSESTT00000000298 Transcript intron_variant - - - - - - rs8024848 15:57021195 T 54816 NM_017661.2 Transcript intron_variant - - - - - - rs8024848 15:57021195 T ENSESTG00000000112 ENSESTT00000000293 Transcript intron_variant - - - - - - rs8024848 15:57021195 T 54816 NM_001002843.1 Transcript intron_variant - - - - - - rs8024848 15:57021195 T 54816 NM_001002844.1 Transcript intron_variant - - - - - - rs6493887 15:57027264 T ENSESTG00000000112 ENSESTT00000000294 Transcript upstream_gene_variant - - - - - - DISTANCE=1427 rs6493887 15:57027264 T ENSESTG00000000112 ENSESTT00000000295 Transcript upstream_gene_variant - - - - - - DISTANCE=1427 rs6493887 15:57027264 T ENSESTG00000000112 ENSESTT00000000298 Transcript upstream_gene_variant - - - - - - DISTANCE=1536 rs6493887 15:57027264 T 54816 NM_017661.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1477 rs6493887 15:57027264 T ENSESTG00000000112 ENSESTT00000000293 Transcript upstream_gene_variant - - - - - - DISTANCE=1427 rs6493887 15:57027264 T 54816 NM_001002843.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1477 rs6493887 15:57027264 T 54816 NM_001002844.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1477 rs11071289 15:57029739 G - ENSR00000408416 RegulatoryFeature regulatory_region_variant - - - - - - rs11071289 15:57029739 G ENSESTG00000000112 ENSESTT00000000294 Transcript upstream_gene_variant - - - - - - DISTANCE=3902 rs11071289 15:57029739 G ENSESTG00000000112 ENSESTT00000000295 Transcript upstream_gene_variant - - - - - - DISTANCE=3902 rs11071289 15:57029739 G ENSESTG00000000112 ENSESTT00000000298 Transcript upstream_gene_variant - - - - - - DISTANCE=4011 rs11071289 15:57029739 G 54816 NM_017661.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3952 rs11071289 15:57029739 G ENSESTG00000000112 ENSESTT00000000293 Transcript upstream_gene_variant - - - - - - DISTANCE=3902 rs11071289 15:57029739 G 54816 NM_001002843.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3952 rs11071289 15:57029739 G 54816 NM_001002844.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3952 rs1972670 15:57071152 G - ENSR00001452422 RegulatoryFeature regulatory_region_variant - - - - - - rs1972670 15:57071152 G - - - intergenic_variant - - - - - - rs1660967 15:57090324 C - - - intergenic_variant - - - - - - rs1657943 15:57094788 C - - - intergenic_variant - - - - - - rs1616859 15:57157643 G - - - intergenic_variant - - - - - - rs1652745 15:57158529 C - - - intergenic_variant - - - - - - rs1430824 15:57180930 C ENSESTG00000000059 ENSESTT00000000154 Transcript downstream_gene_variant - - - - - - DISTANCE=614 rs1430824 15:57180930 C 145783 NR_015419.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1657924 15:57192908 A 145783 NR_015419.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs213156 15:57228929 A 6938 NM_207036.1 Transcript intron_variant - - - - - - rs213156 15:57228929 A ENSESTG00000000064 ENSESTT00000000188 Transcript intron_variant - - - - - - rs213156 15:57228929 A ENSESTG00000000064 ENSESTT00000000171 Transcript intron_variant - - - - - - rs213156 15:57228929 A ENSESTG00000000064 ENSESTT00000000173 Transcript intron_variant - - - - - - rs213156 15:57228929 A 6938 NM_207038.1 Transcript intron_variant - - - - - - rs213156 15:57228929 A CCDS10160.1 CCDS10160.1 Transcript intron_variant - - - - - - rs213156 15:57228929 A ENSESTG00000000064 ENSESTT00000000180 Transcript intron_variant - - - - - - rs213156 15:57228929 A 6938 NM_003205.3 Transcript intron_variant - - - - - - rs213156 15:57228929 A CCDS10159.1 CCDS10159.1 Transcript intron_variant - - - - - - rs213156 15:57228929 A 6938 NM_207037.1 Transcript intron_variant - - - - - - rs213156 15:57228929 A ENSESTG00000000064 ENSESTT00000000185 Transcript intron_variant - - - - - - rs2566848 15:57302432 G 6938 NM_207036.1 Transcript intron_variant - - - - - - rs2566848 15:57302432 G ENSESTG00000000064 ENSESTT00000000188 Transcript intron_variant - - - - - - rs2566848 15:57302432 G ENSESTG00000000064 ENSESTT00000000171 Transcript intron_variant - - - - - - rs2566848 15:57302432 G ENSESTG00000000064 ENSESTT00000000173 Transcript intron_variant - - - - - - rs2566848 15:57302432 G 6938 NM_207038.1 Transcript intron_variant - - - - - - rs2566848 15:57302432 G CCDS10160.1 CCDS10160.1 Transcript intron_variant - - - - - - rs2566848 15:57302432 G ENSESTG00000000064 ENSESTT00000000180 Transcript intron_variant - - - - - - rs2566848 15:57302432 G 6938 NM_003205.3 Transcript intron_variant - - - - - - rs2566848 15:57302432 G CCDS10159.1 CCDS10159.1 Transcript intron_variant - - - - - - rs2566848 15:57302432 G 6938 NM_207037.1 Transcript intron_variant - - - - - - rs2566848 15:57302432 G ENSESTG00000000064 ENSESTT00000000185 Transcript intron_variant - - - - - - rs2254901 15:57413433 A 6938 NM_207036.1 Transcript intron_variant - - - - - - rs2254901 15:57413433 A ENSESTG00000000064 ENSESTT00000000188 Transcript intron_variant - - - - - - rs2254901 15:57413433 A ENSESTG00000000064 ENSESTT00000000171 Transcript intron_variant - - - - - - rs2254901 15:57413433 A ENSESTG00000000064 ENSESTT00000000190 Transcript intron_variant - - - - - - rs2254901 15:57413433 A ENSESTG00000000064 ENSESTT00000000173 Transcript intron_variant - - - - - - rs2254901 15:57413433 A 6938 NM_207038.1 Transcript intron_variant - - - - - - rs2254901 15:57413433 A CCDS10160.1 CCDS10160.1 Transcript intron_variant - - - - - - rs2254901 15:57413433 A 6938 NM_003205.3 Transcript intron_variant - - - - - - rs2254901 15:57413433 A ENSESTG00000000064 ENSESTT00000000180 Transcript intron_variant - - - - - - rs2254901 15:57413433 A ENSESTG00000000064 ENSESTT00000000191 Transcript intron_variant - - - - - - rs2254901 15:57413433 A CCDS10159.1 CCDS10159.1 Transcript intron_variant - - - - - - rs2254901 15:57413433 A 6938 NM_207037.1 Transcript intron_variant - - - - - - rs2593225 15:57429912 A 6938 NM_207036.1 Transcript intron_variant - - - - - - rs2593225 15:57429912 A ENSESTG00000000064 ENSESTT00000000188 Transcript intron_variant - - - - - - rs2593225 15:57429912 A ENSESTG00000000064 ENSESTT00000000171 Transcript intron_variant - - - - - - rs2593225 15:57429912 A ENSESTG00000000064 ENSESTT00000000190 Transcript intron_variant - - - - - - rs2593225 15:57429912 A ENSESTG00000000064 ENSESTT00000000193 Transcript intron_variant - - - - - - rs2593225 15:57429912 A ENSESTG00000000064 ENSESTT00000000173 Transcript intron_variant - - - - - - rs2593225 15:57429912 A 6938 NM_207038.1 Transcript intron_variant - - - - - - rs2593225 15:57429912 A CCDS10160.1 CCDS10160.1 Transcript intron_variant - - - - - - rs2593225 15:57429912 A 6938 NM_003205.3 Transcript intron_variant - - - - - - rs2593225 15:57429912 A ENSESTG00000000064 ENSESTT00000000180 Transcript intron_variant - - - - - - rs2593225 15:57429912 A ENSESTG00000000064 ENSESTT00000000191 Transcript intron_variant - - - - - - rs2593225 15:57429912 A CCDS10159.1 CCDS10159.1 Transcript intron_variant - - - - - - rs2593225 15:57429912 A 6938 NM_207037.1 Transcript intron_variant - - - - - - rs2615240 15:57430824 G - ENSR00000650673 RegulatoryFeature regulatory_region_variant - - - - - - rs2615240 15:57430824 G 6938 NM_207036.1 Transcript intron_variant - - - - - - rs2615240 15:57430824 G ENSESTG00000000064 ENSESTT00000000188 Transcript intron_variant - - - - - - rs2615240 15:57430824 G ENSESTG00000000064 ENSESTT00000000171 Transcript intron_variant - - - - - - rs2615240 15:57430824 G ENSESTG00000000064 ENSESTT00000000190 Transcript intron_variant - - - - - - rs2615240 15:57430824 G ENSESTG00000000064 ENSESTT00000000193 Transcript intron_variant - - - - - - rs2615240 15:57430824 G ENSESTG00000000064 ENSESTT00000000173 Transcript intron_variant - - - - - - rs2615240 15:57430824 G 6938 NM_207038.1 Transcript intron_variant - - - - - - rs2615240 15:57430824 G CCDS10160.1 CCDS10160.1 Transcript intron_variant - - - - - - rs2615240 15:57430824 G 6938 NM_003205.3 Transcript intron_variant - - - - - - rs2615240 15:57430824 G ENSESTG00000000064 ENSESTT00000000180 Transcript intron_variant - - - - - - rs2615240 15:57430824 G ENSESTG00000000064 ENSESTT00000000191 Transcript intron_variant - - - - - - rs2615240 15:57430824 G CCDS10159.1 CCDS10159.1 Transcript intron_variant - - - - - - rs2615240 15:57430824 G 6938 NM_207037.1 Transcript intron_variant - - - - - - rs2615242 15:57436092 G - ENSR00000237351 RegulatoryFeature regulatory_region_variant - - - - - - rs2615242 15:57436092 G 6938 NM_207036.1 Transcript intron_variant - - - - - - rs2615242 15:57436092 G ENSESTG00000000064 ENSESTT00000000188 Transcript intron_variant - - - - - - rs2615242 15:57436092 G ENSESTG00000000064 ENSESTT00000000171 Transcript intron_variant - - - - - - rs2615242 15:57436092 G ENSESTG00000000064 ENSESTT00000000190 Transcript intron_variant - - - - - - rs2615242 15:57436092 G ENSESTG00000000064 ENSESTT00000000193 Transcript intron_variant - - - - - - rs2615242 15:57436092 G ENSESTG00000000064 ENSESTT00000000173 Transcript intron_variant - - - - - - rs2615242 15:57436092 G 6938 NM_207038.1 Transcript intron_variant - - - - - - rs2615242 15:57436092 G CCDS10160.1 CCDS10160.1 Transcript intron_variant - - - - - - rs2615242 15:57436092 G 6938 NM_003205.3 Transcript intron_variant - - - - - - rs2615242 15:57436092 G ENSESTG00000000064 ENSESTT00000000180 Transcript intron_variant - - - - - - rs2615242 15:57436092 G ENSESTG00000000064 ENSESTT00000000191 Transcript intron_variant - - - - - - rs2615242 15:57436092 G CCDS10159.1 CCDS10159.1 Transcript intron_variant - - - - - - rs2615242 15:57436092 G 6938 NM_207037.1 Transcript intron_variant - - - - - - rs1462158 15:57485956 C 6938 NM_207036.1 Transcript intron_variant - - - - - - rs1462158 15:57485956 C ENSESTG00000000064 ENSESTT00000000188 Transcript intron_variant - - - - - - rs1462158 15:57485956 C ENSESTG00000000064 ENSESTT00000000171 Transcript intron_variant - - - - - - rs1462158 15:57485956 C ENSESTG00000000064 ENSESTT00000000190 Transcript intron_variant - - - - - - rs1462158 15:57485956 C ENSESTG00000000064 ENSESTT00000000193 Transcript intron_variant - - - - - - rs1462158 15:57485956 C ENSESTG00000000064 ENSESTT00000000173 Transcript intron_variant - - - - - - rs1462158 15:57485956 C 6938 NM_207038.1 Transcript intron_variant - - - - - - rs1462158 15:57485956 C CCDS10160.1 CCDS10160.1 Transcript intron_variant - - - - - - rs1462158 15:57485956 C 6938 NM_003205.3 Transcript intron_variant - - - - - - rs1462158 15:57485956 C ENSESTG00000000064 ENSESTT00000000180 Transcript intron_variant - - - - - - rs1462158 15:57485956 C ENSESTG00000000064 ENSESTT00000000191 Transcript intron_variant - - - - - - rs1462158 15:57485956 C CCDS10159.1 CCDS10159.1 Transcript intron_variant - - - - - - rs1462158 15:57485956 C 6938 NM_207037.1 Transcript intron_variant - - - - - - rs2544139 15:57626366 A - - - intergenic_variant - - - - - - rs1664445 15:57689457 T ENSESTG00000000101 ENSESTT00000000271 Transcript intron_variant - - - - - - rs1664445 15:57689457 T 84952 NM_001252335.1 Transcript intron_variant - - - - - - rs1664445 15:57689457 T ENSESTG00000000101 ENSESTT00000000261 Transcript intron_variant - - - - - - rs1664445 15:57689457 T 84952 NM_032866.4 Transcript intron_variant - - - - - - rs12902059 15:57691887 G ENSESTG00000000101 ENSESTT00000000271 Transcript intron_variant - - - - - - rs12902059 15:57691887 G 84952 NM_001252335.1 Transcript intron_variant - - - - - - rs12902059 15:57691887 G ENSESTG00000000101 ENSESTT00000000261 Transcript intron_variant - - - - - - rs12902059 15:57691887 G 84952 NM_032866.4 Transcript intron_variant - - - - - - rs1664437 15:57707326 C ENSESTG00000000101 ENSESTT00000000271 Transcript intron_variant - - - - - - rs1664437 15:57707326 C 84952 NM_001252335.1 Transcript intron_variant - - - - - - rs1664437 15:57707326 C ENSESTG00000000101 ENSESTT00000000261 Transcript intron_variant - - - - - - rs1664437 15:57707326 C 84952 NM_032866.4 Transcript intron_variant - - - - - - rs1280363 15:57813262 T ENSESTG00000016662 ENSESTT00000041791 Transcript intron_variant - - - - - - rs1280363 15:57813262 T 84952 NM_001252335.1 Transcript intron_variant - - - - - - rs1280363 15:57813262 T CCDS10161.1 CCDS10161.1 Transcript intron_variant - - - - - - rs1280363 15:57813262 T 84952 NM_032866.4 Transcript intron_variant - - - - - - rs2958059 15:57918090 G CCDS42043.1 CCDS42043.1 Transcript splice_region_variant,synonymous_variant 525 525 175 Q caA/caG - rs2958059 15:57918090 G ENSESTG00000016725 ENSESTT00000042055 Transcript splice_region_variant,synonymous_variant 567 525 175 Q caA/caG - rs2958059 15:57918090 G ENSESTG00000016725 ENSESTT00000042077 Transcript splice_region_variant,synonymous_variant 650 480 160 Q caA/caG - rs2958059 15:57918090 G CCDS42044.1 CCDS42044.1 Transcript splice_region_variant,synonymous_variant 525 525 175 Q caA/caG - rs2958059 15:57918090 G ENSESTG00000016725 ENSESTT00000042062 Transcript splice_region_variant,synonymous_variant 567 525 175 Q caA/caG - rs2958059 15:57918090 G 100820829 NM_152451.6 Transcript splice_region_variant,synonymous_variant 656 525 175 Q caA/caG - rs2958059 15:57918090 G ENSESTG00000016725 ENSESTT00000042087 Transcript splice_region_variant,synonymous_variant 650 480 160 Q caA/caG - rs2958059 15:57918090 G ENSESTG00000016725 ENSESTT00000042073 Transcript splice_region_variant,synonymous_variant 650 480 160 Q caA/caG - rs2958059 15:57918090 G CCDS10162.1 CCDS10162.1 Transcript splice_region_variant,synonymous_variant 525 525 175 Q caA/caG - rs2958059 15:57918090 G 100820829 NM_001018100.3 Transcript splice_region_variant,synonymous_variant 656 525 175 Q caA/caG - rs2958059 15:57918090 G 145781 NM_001018091.4 Transcript splice_region_variant,synonymous_variant 656 525 175 Q caA/caG - rs2958059 15:57918090 G 145781 NM_001018090.4 Transcript splice_region_variant,synonymous_variant 656 525 175 Q caA/caG - rs2958059 15:57918090 G ENSESTG00000016725 ENSESTT00000042033 Transcript splice_region_variant,synonymous_variant 567 525 175 Q caA/caG - rs2958059 15:57918090 G CCDS32247.1 CCDS32247.1 Transcript splice_region_variant,synonymous_variant 525 525 175 Q caA/caG - rs1991252 15:57967219 C ENSESTG00000016725 ENSESTT00000042055 Transcript 3_prime_UTR_variant 1139 - - - - - rs1991252 15:57967219 C ENSESTG00000016725 ENSESTT00000042077 Transcript 3_prime_UTR_variant 1222 - - - - - rs1991252 15:57967219 C CCDS42044.1 CCDS42044.1 Transcript synonymous_variant 1173 1173 391 T acT/acC - rs1991252 15:57967219 C ENSESTG00000016725 ENSESTT00000042098 Transcript 5_prime_UTR_variant 140 - - - - - rs1991252 15:57967219 C ENSESTG00000016725 ENSESTT00000042062 Transcript intron_variant - - - - - - rs1991252 15:57967219 C 100820829 NM_152451.6 Transcript synonymous_variant 1304 1173 391 T acT/acC - rs1991252 15:57967219 C ENSESTG00000016725 ENSESTT00000042073 Transcript synonymous_variant 1382 1212 404 T acT/acC - rs1991252 15:57967219 C ENSESTG00000016725 ENSESTT00000042092 Transcript synonymous_variant 584 546 182 T acT/acC - rs1991252 15:57967219 C CCDS42043.1 CCDS42043.1 Transcript synonymous_variant 1257 1257 419 T acT/acC - rs1991252 15:57967219 C ENSESTG00000016725 ENSESTT00000042087 Transcript intron_variant - - - - - - rs1991252 15:57967219 C ENSESTG00000016725 ENSESTT00000042094 Transcript intron_variant - - - - - - rs1991252 15:57967219 C 100820829 NM_001018100.3 Transcript synonymous_variant 1388 1257 419 T acT/acC - rs1991252 15:57967219 C CCDS10162.1 CCDS10162.1 Transcript synonymous_variant 1257 1257 419 T acT/acC - rs1991252 15:57967219 C ENSESTG00000016725 ENSESTT00000042033 Transcript synonymous_variant 1299 1257 419 T acT/acC - rs1991252 15:57967219 C 145781 NM_001018090.4 Transcript synonymous_variant 1388 1257 419 T acT/acC - rs1991252 15:57967219 C 145781 NM_001018091.4 Transcript synonymous_variant 1388 1257 419 T acT/acC - rs1991252 15:57967219 C CCDS32247.1 CCDS32247.1 Transcript synonymous_variant 1257 1257 419 T acT/acC - rs6493969 15:58207520 G - - - intergenic_variant - - - - - - rs6494008 15:58757770 G CCDS10166.1 CCDS10166.1 Transcript intron_variant - - - - - - rs6494008 15:58757770 G 3990 NM_000236.2 Transcript intron_variant - - - - - - rs6494008 15:58757770 G ENSESTG00000016986 ENSESTT00000042645 Transcript intron_variant - - - - - - rs6494008 15:58757770 G ENSESTG00000016986 ENSESTT00000042691 Transcript intron_variant - - - - - - rs6494008 15:58757770 G ENSESTG00000016986 ENSESTT00000042679 Transcript intron_variant - - - - - - rs6494008 15:58757770 G ENSESTG00000016986 ENSESTT00000042664 Transcript intron_variant - - - - - - rs11857273 15:58829748 C CCDS10166.1 CCDS10166.1 Transcript intron_variant - - - - - - rs11857273 15:58829748 C 3990 NM_000236.2 Transcript intron_variant - - - - - - rs11857273 15:58829748 C ENSESTG00000016986 ENSESTT00000042645 Transcript intron_variant - - - - - - rs11857273 15:58829748 C ENSESTG00000016986 ENSESTT00000042691 Transcript intron_variant - - - - - - rs11857273 15:58829748 C ENSESTG00000016986 ENSESTT00000042679 Transcript intron_variant - - - - - - rs11857273 15:58829748 C ENSESTG00000016986 ENSESTT00000042664 Transcript intron_variant - - - - - - rs923011 15:59581770 C ENSESTG00000030109 ENSESTT00000075834 Transcript intron_variant - - - - - - rs923011 15:59581770 C ENSESTG00000030109 ENSESTT00000075755 Transcript intron_variant - - - - - - rs923011 15:59581770 C ENSESTG00000030109 ENSESTT00000075828 Transcript intron_variant - - - - - - rs923011 15:59581770 C 4643 NM_004998.3 Transcript intron_variant - - - - - - rs923011 15:59581770 C CCDS32254.1 CCDS32254.1 Transcript intron_variant - - - - - - rs4775151 15:59628676 T ENSESTG00000030109 ENSESTT00000075834 Transcript intron_variant - - - - - - rs4775151 15:59628676 T ENSESTG00000030109 ENSESTT00000075755 Transcript intron_variant - - - - - - rs4775151 15:59628676 T ENSESTG00000030109 ENSESTT00000075828 Transcript intron_variant - - - - - - rs4775151 15:59628676 T 4643 NM_004998.3 Transcript intron_variant - - - - - - rs4775151 15:59628676 T CCDS32254.1 CCDS32254.1 Transcript intron_variant - - - - - - rs6494100 15:59636277 G ENSESTG00000030109 ENSESTT00000075834 Transcript intron_variant - - - - - - rs6494100 15:59636277 G ENSESTG00000030109 ENSESTT00000075755 Transcript intron_variant - - - - - - rs6494100 15:59636277 G ENSESTG00000030109 ENSESTT00000075828 Transcript intron_variant - - - - - - rs6494100 15:59636277 G 4643 NM_004998.3 Transcript intron_variant - - - - - - rs6494100 15:59636277 G CCDS32254.1 CCDS32254.1 Transcript intron_variant - - - - - - rs8026056 15:59688164 T ENSESTG00000030092 ENSESTT00000075730 Transcript intron_variant - - - - - - rs8026056 15:59688164 T ENSESTG00000030092 ENSESTT00000075724 Transcript intron_variant - - - - - - rs8026086 15:59688252 G ENSESTG00000030092 ENSESTT00000075730 Transcript intron_variant - - - - - - rs8026086 15:59688252 G ENSESTG00000030092 ENSESTT00000075724 Transcript intron_variant - - - - - - rs9302209 15:59694309 A - ENSR00000408860 RegulatoryFeature regulatory_region_variant - - - - - - rs9302209 15:59694309 A ENSESTG00000030092 ENSESTT00000075730 Transcript intron_variant - - - - - - rs9302209 15:59694309 A ENSESTG00000030092 ENSESTT00000075724 Transcript intron_variant - - - - - - rs6494111 15:59712440 G ENSESTG00000030092 ENSESTT00000075730 Transcript intron_variant - - - - - - rs6494111 15:59712440 G ENSESTG00000030092 ENSESTT00000075724 Transcript intron_variant - - - - - - rs4420473 15:59716092 C ENSESTG00000030092 ENSESTT00000075730 Transcript intron_variant - - - - - - rs4420473 15:59716092 C ENSESTG00000030092 ENSESTT00000075724 Transcript intron_variant - - - - - - rs4390536 15:59791730 T ENSESTG00000009339 ENSESTT00000023432 Transcript intron_variant - - - - - - rs4390536 15:59791730 T CCDS45269.1 CCDS45269.1 Transcript intron_variant - - - - - - rs4390536 15:59791730 T 145773 NM_152450.2 Transcript intron_variant - - - - - - rs12916472 15:59892580 A - - - intergenic_variant - - - - - - rs9888706 15:60044917 T - - - intergenic_variant - - - - - - rs4775208 15:60076327 T - ENSR00001452670 RegulatoryFeature regulatory_region_variant - - - - - - rs4775208 15:60076327 T ENSESTG00000009528 ENSESTT00000023880 Transcript intron_variant - - - - - - rs2960808 15:60173197 G ENSESTG00000009528 ENSESTT00000023880 Transcript intron_variant - - - - - - rs335799 15:60359521 A - - - intergenic_variant - - - - - - rs335796 15:60359933 C - - - intergenic_variant - - - - - - rs335815 15:60364939 C ENSESTG00000009523 ENSESTT00000023874 Transcript downstream_gene_variant - - - - - - DISTANCE=937 rs7495331 15:60414984 T ENSESTG00000009523 ENSESTT00000023874 Transcript upstream_gene_variant - - - - - - DISTANCE=4465 rs2016563 15:60446954 C - - - intergenic_variant - - - - - - rs2219995 15:60447230 G - - - intergenic_variant - - - - - - rs336537 15:60501993 C - - - intergenic_variant - - - - - - rs12913542 15:60600206 A - - - intergenic_variant - - - - - - rs6494205 15:60812203 A - ENSR00000021385 RegulatoryFeature regulatory_region_variant - - - - - - rs6494205 15:60812203 A CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs6494205 15:60812203 A ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs6494205 15:60812203 A CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs6494205 15:60812203 A ENSESTG00000010139 ENSESTT00000025362 Transcript intron_variant - - - - - - rs6494205 15:60812203 A CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs6494205 15:60812203 A ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs6494205 15:60812203 A CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs6494205 15:60812203 A 6095 NM_134262.2 Transcript intron_variant - - - - - - rs6494205 15:60812203 A ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs6494205 15:60812203 A 6095 NM_134260.2 Transcript intron_variant - - - - - - rs6494205 15:60812203 A ENSESTG00000010147 ENSESTT00000025379 Transcript upstream_gene_variant - - - - - - DISTANCE=57 rs6494205 15:60812203 A 6095 NM_002943.3 Transcript intron_variant - - - - - - rs6494205 15:60812203 A 6095 NM_134261.2 Transcript intron_variant - - - - - - rs6494208 15:60815953 C CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs6494208 15:60815953 C ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs6494208 15:60815953 C CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs6494208 15:60815953 C ENSESTG00000010139 ENSESTT00000025362 Transcript intron_variant - - - - - - rs6494208 15:60815953 C CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs6494208 15:60815953 C ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs6494208 15:60815953 C ENSESTG00000010139 ENSESTT00000025370 Transcript upstream_gene_variant - - - - - - DISTANCE=4913 rs6494208 15:60815953 C CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs6494208 15:60815953 C 6095 NM_134262.2 Transcript intron_variant - - - - - - rs6494208 15:60815953 C ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs6494208 15:60815953 C 6095 NM_134260.2 Transcript intron_variant - - - - - - rs6494208 15:60815953 C ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs6494208 15:60815953 C 6095 NM_002943.3 Transcript intron_variant - - - - - - rs6494208 15:60815953 C 6095 NM_134261.2 Transcript intron_variant - - - - - - rs7169846 15:60816773 T CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs7169846 15:60816773 T ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs7169846 15:60816773 T CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs7169846 15:60816773 T ENSESTG00000010139 ENSESTT00000025362 Transcript intron_variant - - - - - - rs7169846 15:60816773 T CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs7169846 15:60816773 T ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs7169846 15:60816773 T ENSESTG00000010139 ENSESTT00000025370 Transcript upstream_gene_variant - - - - - - DISTANCE=4093 rs7169846 15:60816773 T CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs7169846 15:60816773 T 6095 NM_134262.2 Transcript intron_variant - - - - - - rs7169846 15:60816773 T ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs7169846 15:60816773 T 6095 NM_134260.2 Transcript intron_variant - - - - - - rs7169846 15:60816773 T ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs7169846 15:60816773 T 6095 NM_002943.3 Transcript intron_variant - - - - - - rs7169846 15:60816773 T 6095 NM_134261.2 Transcript intron_variant - - - - - - rs4414436 15:60817834 T CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs4414436 15:60817834 T ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs4414436 15:60817834 T CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs4414436 15:60817834 T ENSESTG00000010139 ENSESTT00000025362 Transcript intron_variant - - - - - - rs4414436 15:60817834 T CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs4414436 15:60817834 T ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs4414436 15:60817834 T ENSESTG00000010151 ENSESTT00000025390 Transcript upstream_gene_variant - - - - - - DISTANCE=4348 rs4414436 15:60817834 T ENSESTG00000010139 ENSESTT00000025370 Transcript upstream_gene_variant - - - - - - DISTANCE=3032 rs4414436 15:60817834 T CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs4414436 15:60817834 T 6095 NM_134262.2 Transcript intron_variant - - - - - - rs4414436 15:60817834 T ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs4414436 15:60817834 T 6095 NM_134260.2 Transcript intron_variant - - - - - - rs4414436 15:60817834 T ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs4414436 15:60817834 T 6095 NM_002943.3 Transcript intron_variant - - - - - - rs4414436 15:60817834 T 6095 NM_134261.2 Transcript intron_variant - - - - - - rs4396475 15:60821101 G - ENSR00000409029 RegulatoryFeature regulatory_region_variant - - - - - - rs4396475 15:60821101 G CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs4396475 15:60821101 G ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs4396475 15:60821101 G CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs4396475 15:60821101 G ENSESTG00000010139 ENSESTT00000025362 Transcript intron_variant - - - - - - rs4396475 15:60821101 G CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs4396475 15:60821101 G ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs4396475 15:60821101 G ENSESTG00000010151 ENSESTT00000025390 Transcript upstream_gene_variant - - - - - - DISTANCE=1081 rs4396475 15:60821101 G ENSESTG00000010139 ENSESTT00000025370 Transcript intron_variant - - - - - - rs4396475 15:60821101 G CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs4396475 15:60821101 G 6095 NM_134262.2 Transcript intron_variant - - - - - - rs4396475 15:60821101 G ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs4396475 15:60821101 G 6095 NM_134260.2 Transcript intron_variant - - - - - - rs4396475 15:60821101 G ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs4396475 15:60821101 G 6095 NM_002943.3 Transcript intron_variant - - - - - - rs4396475 15:60821101 G 6095 NM_134261.2 Transcript intron_variant - - - - - - rs10851682 15:60824108 C CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs10851682 15:60824108 C ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs10851682 15:60824108 C CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs10851682 15:60824108 C ENSESTG00000010139 ENSESTT00000025362 Transcript downstream_gene_variant - - - - - - DISTANCE=2182 rs10851682 15:60824108 C CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs10851682 15:60824108 C ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs10851682 15:60824108 C ENSESTG00000010151 ENSESTT00000025390 Transcript intron_variant - - - - - - rs10851682 15:60824108 C ENSESTG00000010139 ENSESTT00000025370 Transcript intron_variant - - - - - - rs10851682 15:60824108 C CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs10851682 15:60824108 C 6095 NM_134262.2 Transcript intron_variant - - - - - - rs10851682 15:60824108 C ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs10851682 15:60824108 C 6095 NM_134260.2 Transcript intron_variant - - - - - - rs10851682 15:60824108 C ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs10851682 15:60824108 C 6095 NM_002943.3 Transcript intron_variant - - - - - - rs10851682 15:60824108 C 6095 NM_134261.2 Transcript intron_variant - - - - - - rs10851683 15:60824544 A CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs10851683 15:60824544 A ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs10851683 15:60824544 A CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs10851683 15:60824544 A ENSESTG00000010139 ENSESTT00000025362 Transcript downstream_gene_variant - - - - - - DISTANCE=2618 rs10851683 15:60824544 A CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs10851683 15:60824544 A ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs10851683 15:60824544 A ENSESTG00000010151 ENSESTT00000025390 Transcript intron_variant - - - - - - rs10851683 15:60824544 A ENSESTG00000010139 ENSESTT00000025370 Transcript intron_variant - - - - - - rs10851683 15:60824544 A CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs10851683 15:60824544 A 6095 NM_134262.2 Transcript intron_variant - - - - - - rs10851683 15:60824544 A ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs10851683 15:60824544 A 6095 NM_134260.2 Transcript intron_variant - - - - - - rs10851683 15:60824544 A ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs10851683 15:60824544 A 6095 NM_002943.3 Transcript intron_variant - - - - - - rs10851683 15:60824544 A 6095 NM_134261.2 Transcript intron_variant - - - - - - rs10775175 15:60824775 G CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs10775175 15:60824775 G ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs10775175 15:60824775 G CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs10775175 15:60824775 G ENSESTG00000010139 ENSESTT00000025362 Transcript downstream_gene_variant - - - - - - DISTANCE=2849 rs10775175 15:60824775 G CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs10775175 15:60824775 G ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs10775175 15:60824775 G ENSESTG00000010151 ENSESTT00000025390 Transcript intron_variant - - - - - - rs10775175 15:60824775 G ENSESTG00000010139 ENSESTT00000025370 Transcript intron_variant - - - - - - rs10775175 15:60824775 G CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs10775175 15:60824775 G 6095 NM_134262.2 Transcript intron_variant - - - - - - rs10775175 15:60824775 G ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs10775175 15:60824775 G 6095 NM_134260.2 Transcript intron_variant - - - - - - rs10775175 15:60824775 G ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs10775175 15:60824775 G 6095 NM_002943.3 Transcript intron_variant - - - - - - rs10775175 15:60824775 G 6095 NM_134261.2 Transcript intron_variant - - - - - - rs4479168 15:60825352 C CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs4479168 15:60825352 C ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs4479168 15:60825352 C CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs4479168 15:60825352 C ENSESTG00000010139 ENSESTT00000025362 Transcript downstream_gene_variant - - - - - - DISTANCE=3426 rs4479168 15:60825352 C CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs4479168 15:60825352 C ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs4479168 15:60825352 C ENSESTG00000010151 ENSESTT00000025390 Transcript intron_variant - - - - - - rs4479168 15:60825352 C ENSESTG00000010139 ENSESTT00000025370 Transcript intron_variant - - - - - - rs4479168 15:60825352 C CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs4479168 15:60825352 C 6095 NM_134262.2 Transcript intron_variant - - - - - - rs4479168 15:60825352 C ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs4479168 15:60825352 C 6095 NM_134260.2 Transcript intron_variant - - - - - - rs4479168 15:60825352 C ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs4479168 15:60825352 C 6095 NM_002943.3 Transcript intron_variant - - - - - - rs4479168 15:60825352 C 6095 NM_134261.2 Transcript intron_variant - - - - - - rs8027050 15:60833987 G CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs8027050 15:60833987 G ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs8027050 15:60833987 G CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs8027050 15:60833987 G CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs8027050 15:60833987 G ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs8027050 15:60833987 G ENSESTG00000010151 ENSESTT00000025390 Transcript intron_variant - - - - - - rs8027050 15:60833987 G ENSESTG00000010139 ENSESTT00000025370 Transcript intron_variant - - - - - - rs8027050 15:60833987 G CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs8027050 15:60833987 G 6095 NM_134262.2 Transcript intron_variant - - - - - - rs8027050 15:60833987 G ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs8027050 15:60833987 G 6095 NM_134260.2 Transcript intron_variant - - - - - - rs8027050 15:60833987 G ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs8027050 15:60833987 G 6095 NM_002943.3 Transcript intron_variant - - - - - - rs8027050 15:60833987 G 6095 NM_134261.2 Transcript intron_variant - - - - - - rs8023943 15:60836768 C CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs8023943 15:60836768 C ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs8023943 15:60836768 C CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs8023943 15:60836768 C CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs8023943 15:60836768 C ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs8023943 15:60836768 C ENSESTG00000010151 ENSESTT00000025390 Transcript intron_variant - - - - - - rs8023943 15:60836768 C ENSESTG00000010139 ENSESTT00000025370 Transcript stop_lost 257 153 51 */Y taG/taC - rs8023943 15:60836768 C CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs8023943 15:60836768 C 6095 NM_134262.2 Transcript intron_variant - - - - - - rs8023943 15:60836768 C ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs8023943 15:60836768 C 6095 NM_134260.2 Transcript intron_variant - - - - - - rs8023943 15:60836768 C ENSESTG00000010147 ENSESTT00000025379 Transcript intron_variant - - - - - - rs8023943 15:60836768 C 6095 NM_002943.3 Transcript intron_variant - - - - - - rs8023943 15:60836768 C 6095 NM_134261.2 Transcript intron_variant - - - - - - rs6494210 15:60840107 C CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs6494210 15:60840107 C ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs6494210 15:60840107 C CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs6494210 15:60840107 C CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs6494210 15:60840107 C ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs6494210 15:60840107 C ENSESTG00000010151 ENSESTT00000025390 Transcript downstream_gene_variant - - - - - - DISTANCE=2748 rs6494210 15:60840107 C ENSESTG00000010139 ENSESTT00000025370 Transcript downstream_gene_variant - - - - - - DISTANCE=3273 rs6494210 15:60840107 C CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs6494210 15:60840107 C 6095 NM_134262.2 Transcript intron_variant - - - - - - rs6494210 15:60840107 C ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs6494210 15:60840107 C 6095 NM_134260.2 Transcript intron_variant - - - - - - rs6494210 15:60840107 C ENSESTG00000010147 ENSESTT00000025379 Transcript missense_variant 628 77 26 M/T aTg/aCg - rs6494210 15:60840107 C 6095 NM_002943.3 Transcript intron_variant - - - - - - rs6494210 15:60840107 C 6095 NM_134261.2 Transcript intron_variant - - - - - - rs7165455 15:60846172 C CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs7165455 15:60846172 C ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs7165455 15:60846172 C CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs7165455 15:60846172 C CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs7165455 15:60846172 C ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs7165455 15:60846172 C CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs7165455 15:60846172 C 6095 NM_134262.2 Transcript intron_variant - - - - - - rs7165455 15:60846172 C ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs7165455 15:60846172 C 6095 NM_134260.2 Transcript intron_variant - - - - - - rs7165455 15:60846172 C 6095 NM_002943.3 Transcript intron_variant - - - - - - rs7165455 15:60846172 C 6095 NM_134261.2 Transcript intron_variant - - - - - - rs4774369 15:60850320 T CCDS45271.1 CCDS45271.1 Transcript intron_variant - - - - - - rs4774369 15:60850320 T ENSESTG00000010199 ENSESTT00000025495 Transcript intron_variant - - - - - - rs4774369 15:60850320 T CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs4774369 15:60850320 T CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs4774369 15:60850320 T ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs4774369 15:60850320 T CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs4774369 15:60850320 T 6095 NM_134262.2 Transcript intron_variant - - - - - - rs4774369 15:60850320 T ENSESTG00000010199 ENSESTT00000025493 Transcript intron_variant - - - - - - rs4774369 15:60850320 T 6095 NM_134260.2 Transcript intron_variant - - - - - - rs4774369 15:60850320 T 6095 NM_002943.3 Transcript intron_variant - - - - - - rs4774369 15:60850320 T 6095 NM_134261.2 Transcript intron_variant - - - - - - rs186857 15:60911613 T CCDS10178.1 CCDS10178.1 Transcript intron_variant - - - - - - rs186857 15:60911613 T ENSESTG00000010199 ENSESTT00000025488 Transcript intron_variant - - - - - - rs186857 15:60911613 T CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs186857 15:60911613 T CCDS10179.1 CCDS10179.1 Transcript intron_variant - - - - - - rs186857 15:60911613 T 6095 NM_134260.2 Transcript intron_variant - - - - - - rs186857 15:60911613 T 6095 NM_134261.2 Transcript intron_variant - - - - - - rs186857 15:60911613 T 6095 NM_002943.3 Transcript intron_variant - - - - - - rs9920400 15:60977322 T ENSESTG00000010157 ENSESTT00000025415 Transcript intron_variant - - - - - - rs9920400 15:60977322 T CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs9920400 15:60977322 T ENSESTG00000010157 ENSESTT00000025407 Transcript intron_variant - - - - - - rs9920400 15:60977322 T 6095 NM_134261.2 Transcript intron_variant - - - - - - rs2162068 15:60978842 T ENSESTG00000010157 ENSESTT00000025415 Transcript intron_variant - - - - - - rs2162068 15:60978842 T CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs2162068 15:60978842 T ENSESTG00000010157 ENSESTT00000025407 Transcript intron_variant - - - - - - rs2162068 15:60978842 T 6095 NM_134261.2 Transcript intron_variant - - - - - - rs2613621 15:61015852 G CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs2613621 15:61015852 G 6095 NM_134261.2 Transcript intron_variant - - - - - - rs341412 15:61029269 C CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs341412 15:61029269 C 6095 NM_134261.2 Transcript intron_variant - - - - - - rs341416 15:61033178 T - ENSR00001452743 RegulatoryFeature regulatory_region_variant - - - - - - rs341416 15:61033178 T CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs341416 15:61033178 T 6095 NM_134261.2 Transcript intron_variant - - - - - - rs782922 15:61402696 T CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs782922 15:61402696 T ENSESTG00000010183 ENSESTT00000025459 Transcript intron_variant - - - - - - rs782922 15:61402696 T 6095 NM_134261.2 Transcript intron_variant - - - - - - rs75965534 15:61427061 C CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs75965534 15:61427061 C ENSESTG00000010183 ENSESTT00000025459 Transcript intron_variant - - - - - - rs75965534 15:61427061 C 6095 NM_134261.2 Transcript intron_variant - - - - - - rs2414693 15:61502308 C CCDS10177.1 CCDS10177.1 Transcript intron_variant - - - - - - rs2414693 15:61502308 C ENSESTG00000010183 ENSESTT00000025459 Transcript intron_variant - - - - - - rs2414693 15:61502308 C ENSESTG00000010183 ENSESTT00000025466 Transcript intron_variant - - - - - - rs2414693 15:61502308 C ENSESTG00000010178 ENSESTT00000025444 Transcript upstream_gene_variant - - - - - - DISTANCE=1804 rs2414693 15:61502308 C 6095 NM_134261.2 Transcript intron_variant - - - - - - rs4591067 15:61760894 T - - - intergenic_variant - - - - - - rs4775439 15:62120672 G - - - intergenic_variant - - - - - - rs6494304 15:62357781 C CCDS32258.1 CCDS32258.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2032 rs6494304 15:62357781 C 145741 NM_207322.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1395 rs6494304 15:62357781 C ENSESTG00000031854 ENSESTT00000080380 Transcript upstream_gene_variant - - - - - - DISTANCE=1395 rs6494304 15:62357781 C ENSESTG00000031845 ENSESTT00000080343 Transcript downstream_gene_variant - - - - - - DISTANCE=4320 rs7402469 15:62374729 G - - - intergenic_variant - - - - - - rs2916859 15:62734823 G - - - intergenic_variant - - - - - - rs780146 15:62766951 T ENSESTG00000007733 ENSESTT00000019494 Transcript intron_variant - - - - - - rs4530074 15:62962232 A ENSESTG00000007740 ENSESTT00000019548 Transcript upstream_gene_variant - - - - - - DISTANCE=3825 rs4530074 15:62962232 A 83660 NM_015059.2 Transcript intron_variant - - - - - - rs4530074 15:62962232 A CCDS32261.1 CCDS32261.1 Transcript intron_variant - - - - - - rs902026 15:63218307 C - - - intergenic_variant - - - - - - rs2414798 15:63225681 C - ENSR00001452919 RegulatoryFeature regulatory_region_variant - - - - - - rs2414798 15:63225681 C - - - intergenic_variant - - - - - - rs8040971 15:63243361 G - - - intergenic_variant - - - - - - rs10851720 15:63290465 G - ENSR00001452934 RegulatoryFeature regulatory_region_variant - - - - - - rs10851720 15:63290465 G - - - intergenic_variant - - - - - - rs4259998 15:63296068 C - ENSR00001452936 RegulatoryFeature regulatory_region_variant - - - - - - rs4259998 15:63296068 C - - - intergenic_variant - - - - - - rs4775618 15:63388586 C - - - intergenic_variant - - - - - - rs2588858 15:63465428 C - - - intergenic_variant - - - - - - rs2134266 15:63487925 T - ENSR00000237601 RegulatoryFeature regulatory_region_variant - - - - - - rs2134266 15:63487925 T ENSESTG00000007939 ENSESTT00000020113 Transcript intron_variant - - - - - - rs2134266 15:63487925 T CCDS10183.1 CCDS10183.1 Transcript intron_variant - - - - - - rs2134266 15:63487925 T ENSESTG00000007939 ENSESTT00000020117 Transcript intron_variant - - - - - - rs2134266 15:63487925 T 51762 NM_016530.2 Transcript intron_variant - - - - - - rs2134266 15:63487925 T ENSESTG00000007939 ENSESTT00000020102 Transcript intron_variant - - - - - - rs8029378 15:63512074 G ENSESTG00000007939 ENSESTT00000020113 Transcript intron_variant - - - - - - rs8029378 15:63512074 G CCDS10183.1 CCDS10183.1 Transcript intron_variant - - - - - - rs8029378 15:63512074 G ENSESTG00000007939 ENSESTT00000020117 Transcript intron_variant - - - - - - rs8029378 15:63512074 G 51762 NM_016530.2 Transcript intron_variant - - - - - - rs8029378 15:63512074 G ENSESTG00000007939 ENSESTT00000020102 Transcript intron_variant - - - - - - rs4377108 15:63625790 A CCDS10185.1 CCDS10185.1 Transcript intron_variant - - - - - - rs4377108 15:63625790 A ENSESTG00000008011 ENSESTT00000020316 Transcript intron_variant - - - - - - rs4377108 15:63625790 A 771 NM_001218.3 Transcript intron_variant - - - - - - rs4377108 15:63625790 A ENSESTG00000008011 ENSESTT00000020322 Transcript upstream_gene_variant - - - - - - DISTANCE=1778 rs4377108 15:63625790 A CCDS10186.1 CCDS10186.1 Transcript intron_variant - - - - - - rs4377108 15:63625790 A 771 NM_206925.1 Transcript intron_variant - - - - - - rs4312261 15:63625796 A CCDS10185.1 CCDS10185.1 Transcript intron_variant - - - - - - rs4312261 15:63625796 A ENSESTG00000008011 ENSESTT00000020316 Transcript intron_variant - - - - - - rs4312261 15:63625796 A 771 NM_001218.3 Transcript intron_variant - - - - - - rs4312261 15:63625796 A ENSESTG00000008011 ENSESTT00000020322 Transcript upstream_gene_variant - - - - - - DISTANCE=1784 rs4312261 15:63625796 A CCDS10186.1 CCDS10186.1 Transcript intron_variant - - - - - - rs4312261 15:63625796 A 771 NM_206925.1 Transcript intron_variant - - - - - - rs7402318 15:63934142 G 8925 NM_003922.3 Transcript intron_variant - - - - - - rs7402318 15:63934142 G ENSESTG00000008871 ENSESTT00000022257 Transcript downstream_gene_variant - - - - - - DISTANCE=3603 rs7402318 15:63934142 G CCDS45277.1 CCDS45277.1 Transcript intron_variant - - - - - - rs8034053 15:64092183 A 8925 NM_003922.3 Transcript intron_variant - - - - - - rs8034053 15:64092183 A ENSESTG00000008851 ENSESTT00000022220 Transcript intron_variant - - - - - - rs8034053 15:64092183 A ENSESTG00000008851 ENSESTT00000022216 Transcript intron_variant - - - - - - rs4776706 15:64294592 T ENSESTG00000008834 ENSESTT00000022183 Transcript intron_variant - - - - - - rs4776706 15:64294592 T 23604 NM_014326.3 Transcript intron_variant - - - - - - rs4776706 15:64294592 T CCDS10188.1 CCDS10188.1 Transcript intron_variant - - - - - - rs332250 15:64363943 C - ENSR00001453021 RegulatoryFeature regulatory_region_variant - - - - - - rs332250 15:64363943 C CCDS45278.1 CCDS45278.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3774 rs332250 15:64363943 C ENSESTG00000008811 ENSESTT00000022155 Transcript downstream_gene_variant - - - - - - DISTANCE=1063 rs332250 15:64363943 C CCDS10189.1 CCDS10189.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1187 rs332250 15:64363943 C 84191 NM_001014812.1 Transcript downstream_gene_variant - - - - - - DISTANCE=818 rs332250 15:64363943 C 84191 NM_032231.4 Transcript downstream_gene_variant - - - - - - DISTANCE=818 rs332251 15:64363958 C - ENSR00001453021 RegulatoryFeature regulatory_region_variant - - - - - - rs332251 15:64363958 C CCDS45278.1 CCDS45278.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3759 rs332251 15:64363958 C ENSESTG00000008811 ENSESTT00000022155 Transcript downstream_gene_variant - - - - - - DISTANCE=1048 rs332251 15:64363958 C CCDS10189.1 CCDS10189.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1172 rs332251 15:64363958 C 84191 NM_001014812.1 Transcript downstream_gene_variant - - - - - - DISTANCE=803 rs332251 15:64363958 C 84191 NM_032231.4 Transcript downstream_gene_variant - - - - - - DISTANCE=803 rs332253 15:64364890 A - ENSR00001453021 RegulatoryFeature regulatory_region_variant - - - - - - rs332253 15:64364890 A CCDS45278.1 CCDS45278.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2827 rs332253 15:64364890 A ENSESTG00000008811 ENSESTT00000022155 Transcript downstream_gene_variant - - - - - - DISTANCE=116 rs332253 15:64364890 A CCDS10189.1 CCDS10189.1 Transcript downstream_gene_variant - - - - - - DISTANCE=240 rs332253 15:64364890 A 84191 NM_001014812.1 Transcript 3_prime_UTR_variant 913 - - - - - rs332253 15:64364890 A 84191 NM_032231.4 Transcript 3_prime_UTR_variant 963 - - - - - rs2926688 15:64369089 G CCDS45278.1 CCDS45278.1 Transcript intron_variant - - - - - - rs2926688 15:64369089 G ENSESTG00000008811 ENSESTT00000022155 Transcript intron_variant - - - - - - rs2926688 15:64369089 G CCDS10189.1 CCDS10189.1 Transcript intron_variant - - - - - - rs2926688 15:64369089 G 84191 NM_001014812.1 Transcript intron_variant - - - - - - rs2926688 15:64369089 G 84191 NM_032231.4 Transcript intron_variant - - - - - - rs3848146 15:64456160 C - ENSR00000409593 RegulatoryFeature regulatory_region_variant - - - - - - rs3848146 15:64456160 C 53944 NM_022048.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1556 rs3848146 15:64456160 C 5479 NM_000942.4 Transcript upstream_gene_variant - - - - - - DISTANCE=806 rs3848146 15:64456160 C ENSESTG00000008785 ENSESTT00000022109 Transcript upstream_gene_variant - - - - - - DISTANCE=945 rs3848146 15:64456160 C CCDS10191.1 CCDS10191.1 Transcript upstream_gene_variant - - - - - - DISTANCE=975 rs3848146 15:64456160 C ENSESTG00000008785 ENSESTT00000022093 Transcript upstream_gene_variant - - - - - - DISTANCE=939 rs4776960 15:64466251 G 53944 NM_022048.3 Transcript intron_variant - - - - - - rs4776960 15:64466251 G ENSESTG00000008732 ENSESTT00000022016 Transcript intron_variant - - - - - - rs4776960 15:64466251 G ENSESTG00000008732 ENSESTT00000022043 Transcript intron_variant - - - - - - rs4776960 15:64466251 G CCDS10192.2 CCDS10192.2 Transcript intron_variant - - - - - - rs4776960 15:64466251 G ENSESTG00000008732 ENSESTT00000022023 Transcript intron_variant - - - - - - rs4776960 15:64466251 G ENSESTG00000008732 ENSESTT00000022005 Transcript intron_variant - - - - - - rs11071787 15:64523341 C 53944 NM_022048.3 Transcript intron_variant - - - - - - rs11071787 15:64523341 C CCDS10192.2 CCDS10192.2 Transcript intron_variant - - - - - - rs11071787 15:64523341 C ENSESTG00000008732 ENSESTT00000022005 Transcript intron_variant - - - - - - rs4238416 15:64552263 A 53944 NM_022048.3 Transcript intron_variant - - - - - - rs4238416 15:64552263 A ENSESTG00000008732 ENSESTT00000021966 Transcript intron_variant - - - - - - rs4238416 15:64552263 A CCDS10192.2 CCDS10192.2 Transcript intron_variant - - - - - - rs4238416 15:64552263 A ENSESTG00000008732 ENSESTT00000022005 Transcript intron_variant - - - - - - rs8024318 15:64909319 A CCDS32270.1 CCDS32270.1 Transcript intron_variant - - - - - - rs8024318 15:64909319 A ENSESTG00000020231 ENSESTT00000050763 Transcript intron_variant - - - - - - rs8024318 15:64909319 A 23060 NM_015042.1 Transcript intron_variant - - - - - - rs4777576 15:65053569 C - ENSR00000409668 RegulatoryFeature regulatory_region_variant - - - - - - rs4777576 15:65053569 C ENSESTG00000020751 ENSESTT00000052113 Transcript intron_variant - - - - - - rs4777576 15:65053569 C 100302184 NR_031674.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1017 rs4777576 15:65053569 C CCDS32271.1 CCDS32271.1 Transcript intron_variant - - - - - - rs4777576 15:65053569 C ENSESTG00000020751 ENSESTT00000052101 Transcript intron_variant - - - - - - rs4777576 15:65053569 C 348093 NM_194272.1 Transcript intron_variant - - - - - - rs2177241 15:65261931 C CCDS10198.1 CCDS10198.1 Transcript intron_variant - - - - - - rs2177241 15:65261931 C ENSESTG00000020660 ENSESTT00000051985 Transcript intron_variant - - - - - - rs2177241 15:65261931 C ENSESTG00000020660 ENSESTT00000051900 Transcript downstream_gene_variant - - - - - - DISTANCE=604 rs2177241 15:65261931 C 51324 NM_001127890.1 Transcript intron_variant - - - - - - rs2177241 15:65261931 C ENSESTG00000020660 ENSESTT00000051998 Transcript downstream_gene_variant - - - - - - DISTANCE=583 rs2177241 15:65261931 C 51324 NM_001127889.1 Transcript intron_variant - - - - - - rs2177241 15:65261931 C CCDS45279.1 CCDS45279.1 Transcript intron_variant - - - - - - rs2177241 15:65261931 C 51324 NM_016630.3 Transcript intron_variant - - - - - - rs2946670 15:65449169 T ENSESTG00000020543 ENSESTT00000051635 Transcript downstream_gene_variant - - - - - - DISTANCE=1815 rs2946670 15:65449169 T 10845 NM_006660.3 Transcript intron_variant - - - - - - rs2946670 15:65449169 T ENSESTG00000020543 ENSESTT00000051596 Transcript downstream_gene_variant - - - - - - DISTANCE=1815 rs2946670 15:65449169 T CCDS10202.1 CCDS10202.1 Transcript intron_variant - - - - - - rs507538 15:65562463 A CCDS10204.1 CCDS10204.1 Transcript intron_variant - - - - - - rs507538 15:65562463 A 54956 NM_017851.4 Transcript intron_variant - - - - - - rs507538 15:65562463 A ENSESTG00000020504 ENSESTT00000051455 Transcript intron_variant - - - - - - rs507538 15:65562463 A ENSESTG00000020504 ENSESTT00000051466 Transcript intron_variant - - - - - - rs507538 15:65562463 A ENSESTG00000020504 ENSESTT00000051428 Transcript intron_variant - - - - - - rs524871 15:65609005 A - - - intergenic_variant - - - - - - rs7168189 15:65672206 C CCDS10206.1 CCDS10206.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4141 rs7168189 15:65672206 C ENSESTG00000020481 ENSESTT00000051352 Transcript upstream_gene_variant - - - - - - DISTANCE=1886 rs7168189 15:65672206 C 57722 NM_020962.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1619 rs7168189 15:65672206 C CCDS10205.1 CCDS10205.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2080 rs7168189 15:65672206 C 9543 NM_004884.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1828 rs2174330 15:65858793 G 51495 NM_016395.2 Transcript intron_variant - - - - - - rs2174330 15:65858793 G CCDS45282.1 CCDS45282.1 Transcript intron_variant - - - - - - rs2174330 15:65858793 G ENSESTG00000019074 ENSESTT00000048218 Transcript intron_variant - - - - - - rs2174330 15:65858793 G ENSESTG00000019074 ENSESTT00000048308 Transcript intron_variant - - - - - - rs2174330 15:65858793 G ENSESTG00000019074 ENSESTT00000048304 Transcript intron_variant - - - - - - rs333576 15:66349177 C ENSESTG00000020306 ENSESTT00000050912 Transcript intron_variant - - - - - - rs333576 15:66349177 C 84465 NM_032445.2 Transcript intron_variant - - - - - - rs333576 15:66349177 C CCDS10213.2 CCDS10213.2 Transcript intron_variant - - - - - - rs1036366 15:66352455 G ENSESTG00000020306 ENSESTT00000050912 Transcript intron_variant - - - - - - rs1036366 15:66352455 G 84465 NM_032445.2 Transcript intron_variant - - - - - - rs1036366 15:66352455 G CCDS10213.2 CCDS10213.2 Transcript intron_variant - - - - - - rs11635806 15:66432077 A ENSESTG00000020306 ENSESTT00000050912 Transcript intron_variant - - - - - - rs11635806 15:66432077 A 84465 NM_032445.2 Transcript intron_variant - - - - - - rs4776753 15:66453678 G ENSESTG00000020306 ENSESTT00000050912 Transcript intron_variant - - - - - - rs4776753 15:66453678 G 84465 NM_032445.2 Transcript intron_variant - - - - - - rs4776777 15:66602797 T ENSESTG00000019823 ENSESTT00000049967 Transcript intron_variant - - - - - - rs4776777 15:66602797 T ENSESTG00000019823 ENSESTT00000050000 Transcript upstream_gene_variant - - - - - - DISTANCE=1344 rs4776777 15:66602797 T ENSESTG00000019823 ENSESTT00000049929 Transcript intron_variant - - - - - - rs4776777 15:66602797 T ENSESTG00000019823 ENSESTT00000049938 Transcript intron_variant - - - - - - rs4776777 15:66602797 T 115752 NM_001143688.1 Transcript intron_variant - - - - - - rs4776777 15:66602797 T ENSESTG00000019823 ENSESTT00000049956 Transcript downstream_gene_variant - - - - - - DISTANCE=1716 rs4776777 15:66602797 T CCDS10214.1 CCDS10214.1 Transcript intron_variant - - - - - - rs4776777 15:66602797 T ENSESTG00000019823 ENSESTT00000049970 Transcript intron_variant - - - - - - rs4776777 15:66602797 T CCDS45286.1 CCDS45286.1 Transcript intron_variant - - - - - - rs4776777 15:66602797 T 115752 NM_133375.3 Transcript intron_variant - - - - - - rs7497898 15:66668952 G ENSESTG00000020084 ENSESTT00000050399 Transcript intron_variant - - - - - - rs28665058 15:66914998 G - ENSR00001453167 RegulatoryFeature regulatory_region_variant - - - - - - rs28665058 15:66914998 G - - - intergenic_variant - - - - - - rs4776820 15:66960529 C - ENSR00000409979 RegulatoryFeature regulatory_region_variant - - - - - - rs4776820 15:66960529 C - - - intergenic_variant - - - - - - rs8038354 15:66969299 C - ENSR00000237880 RegulatoryFeature regulatory_region_variant - - - - - - rs8038354 15:66969299 C - - - intergenic_variant - - - - - - rs2439384 15:67028001 G - ENSR00001453183 RegulatoryFeature regulatory_region_variant - - - - - - rs2439384 15:67028001 G 4091 NM_005585.4 Transcript intron_variant - - - - - - rs2439384 15:67028001 G CCDS10221.1 CCDS10221.1 Transcript intron_variant - - - - - - rs2439384 15:67028001 G ENSESTG00000022911 ENSESTT00000057800 Transcript intron_variant - - - - - - rs2439384 15:67028001 G 4091 NR_027654.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2439384 15:67028001 G 4091 NM_001142861.2 Transcript intron_variant - - - - - - rs2439384 15:67028001 G ENSESTG00000022911 ENSESTT00000057824 Transcript intron_variant - - - - - - rs2439384 15:67028001 G CCDS45287.1 CCDS45287.1 Transcript intron_variant - - - - - - rs266307 15:67315759 T ENSESTG00000023777 ENSESTT00000059949 Transcript intron_variant - - - - - - rs2118609 15:67428479 G ENSESTG00000023050 ENSESTT00000058166 Transcript intron_variant - - - - - - rs2118609 15:67428479 G 4088 NM_001145103.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1880 rs2118609 15:67428479 G CCDS10222.1 CCDS10222.1 Transcript intron_variant - - - - - - rs2118609 15:67428479 G 4088 NM_001145102.1 Transcript intron_variant - - - - - - rs2118609 15:67428479 G 4088 NM_005902.3 Transcript intron_variant - - - - - - rs2118609 15:67428479 G CCDS45288.1 CCDS45288.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1886 rs1347783 15:67429348 T ENSESTG00000023050 ENSESTT00000058166 Transcript intron_variant - - - - - - rs1347783 15:67429348 T 4088 NM_001145103.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1011 rs1347783 15:67429348 T CCDS10222.1 CCDS10222.1 Transcript intron_variant - - - - - - rs1347783 15:67429348 T 4088 NM_001145102.1 Transcript intron_variant - - - - - - rs1347783 15:67429348 T 4088 NM_005902.3 Transcript intron_variant - - - - - - rs1347783 15:67429348 T CCDS45288.1 CCDS45288.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1017 rs4325503 15:67749767 C ENSESTG00000013187 ENSESTT00000033090 Transcript intron_variant - - - - - - rs4325503 15:67749767 C 64799 NM_001031715.2 Transcript intron_variant - - - - - - rs4325503 15:67749767 C 100506686 NR_040051.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4325503 15:67749767 C 100506686 NR_040052.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4325503 15:67749767 C CCDS32273.1 CCDS32273.1 Transcript intron_variant - - - - - - rs4776934 15:67780350 G ENSESTG00000013187 ENSESTT00000033090 Transcript intron_variant - - - - - - rs4776934 15:67780350 G 64799 NM_001031715.2 Transcript intron_variant - - - - - - rs4776934 15:67780350 G 100506686 NR_040051.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4776934 15:67780350 G 100506686 NR_040052.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4776934 15:67780350 G CCDS32273.1 CCDS32273.1 Transcript intron_variant - - - - - - rs4776944 15:67861176 C CCDS42051.1 CCDS42051.1 Transcript intron_variant - - - - - - rs4776944 15:67861176 C ENSESTG00000013213 ENSESTT00000033170 Transcript intron_variant - - - - - - rs4776944 15:67861176 C CCDS10224.1 CCDS10224.1 Transcript intron_variant - - - - - - rs4776944 15:67861176 C ENSESTG00000013213 ENSESTT00000033180 Transcript upstream_gene_variant - - - - - - DISTANCE=1521 rs4776944 15:67861176 C ENSESTG00000013213 ENSESTT00000033176 Transcript intron_variant - - - - - - rs4776944 15:67861176 C 5607 NM_001206804.1 Transcript intron_variant - - - - - - rs4776944 15:67861176 C 5607 NM_002757.3 Transcript intron_variant - - - - - - rs4776944 15:67861176 C 5607 NM_145160.2 Transcript intron_variant - - - - - - rs4776944 15:67861176 C CCDS55970.1 CCDS55970.1 Transcript intron_variant - - - - - - rs4776944 15:67861176 C ENSESTG00000013213 ENSESTT00000033172 Transcript intron_variant - - - - - - rs4776944 15:67861176 C ENSESTG00000013213 ENSESTT00000033178 Transcript intron_variant - - - - - - rs10851776 15:67890357 A CCDS42051.1 CCDS42051.1 Transcript intron_variant - - - - - - rs10851776 15:67890357 A ENSESTG00000013213 ENSESTT00000033192 Transcript intron_variant - - - - - - rs10851776 15:67890357 A ENSESTG00000013213 ENSESTT00000033170 Transcript intron_variant - - - - - - rs10851776 15:67890357 A CCDS10224.1 CCDS10224.1 Transcript intron_variant - - - - - - rs10851776 15:67890357 A ENSESTG00000013213 ENSESTT00000033180 Transcript intron_variant - - - - - - rs10851776 15:67890357 A ENSESTG00000013213 ENSESTT00000033176 Transcript intron_variant - - - - - - rs10851776 15:67890357 A 5607 NM_001206804.1 Transcript intron_variant - - - - - - rs10851776 15:67890357 A 5607 NM_002757.3 Transcript intron_variant - - - - - - rs10851776 15:67890357 A 5607 NM_145160.2 Transcript intron_variant - - - - - - rs10851776 15:67890357 A CCDS55970.1 CCDS55970.1 Transcript intron_variant - - - - - - rs10851776 15:67890357 A ENSESTG00000013213 ENSESTT00000033172 Transcript intron_variant - - - - - - rs10851776 15:67890357 A ENSESTG00000013213 ENSESTT00000033194 Transcript intron_variant - - - - - - rs10851776 15:67890357 A ENSESTG00000013213 ENSESTT00000033178 Transcript intron_variant - - - - - - rs10851776 15:67890357 A ENSESTG00000013213 ENSESTT00000033188 Transcript intron_variant - - - - - - rs6494679 15:67946266 T CCDS42051.1 CCDS42051.1 Transcript intron_variant - - - - - - rs6494679 15:67946266 T ENSESTG00000013213 ENSESTT00000033192 Transcript intron_variant - - - - - - rs6494679 15:67946266 T ENSESTG00000013213 ENSESTT00000033170 Transcript intron_variant - - - - - - rs6494679 15:67946266 T CCDS10224.1 CCDS10224.1 Transcript intron_variant - - - - - - rs6494679 15:67946266 T ENSESTG00000013213 ENSESTT00000033180 Transcript intron_variant - - - - - - rs6494679 15:67946266 T ENSESTG00000013213 ENSESTT00000033176 Transcript intron_variant - - - - - - rs6494679 15:67946266 T 5607 NM_001206804.1 Transcript intron_variant - - - - - - rs6494679 15:67946266 T 5607 NM_002757.3 Transcript intron_variant - - - - - - rs6494679 15:67946266 T 5607 NM_145160.2 Transcript intron_variant - - - - - - rs6494679 15:67946266 T CCDS55970.1 CCDS55970.1 Transcript intron_variant - - - - - - rs6494679 15:67946266 T ENSESTG00000013213 ENSESTT00000033188 Transcript intron_variant - - - - - - rs6494689 15:67982380 A CCDS42051.1 CCDS42051.1 Transcript intron_variant - - - - - - rs6494689 15:67982380 A ENSESTG00000013213 ENSESTT00000033192 Transcript intron_variant - - - - - - rs6494689 15:67982380 A ENSESTG00000013213 ENSESTT00000033170 Transcript intron_variant - - - - - - rs6494689 15:67982380 A CCDS10224.1 CCDS10224.1 Transcript intron_variant - - - - - - rs6494689 15:67982380 A ENSESTG00000013213 ENSESTT00000033180 Transcript intron_variant - - - - - - rs6494689 15:67982380 A ENSESTG00000013213 ENSESTT00000033176 Transcript intron_variant - - - - - - rs6494689 15:67982380 A 5607 NM_001206804.1 Transcript intron_variant - - - - - - rs6494689 15:67982380 A 5607 NM_002757.3 Transcript intron_variant - - - - - - rs6494689 15:67982380 A 5607 NM_145160.2 Transcript intron_variant - - - - - - rs6494689 15:67982380 A CCDS55970.1 CCDS55970.1 Transcript intron_variant - - - - - - rs6494689 15:67982380 A ENSESTG00000013213 ENSESTT00000033188 Transcript intron_variant - - - - - - rs8025055 15:68015751 A CCDS42051.1 CCDS42051.1 Transcript intron_variant - - - - - - rs8025055 15:68015751 A ENSESTG00000013213 ENSESTT00000033192 Transcript intron_variant - - - - - - rs8025055 15:68015751 A ENSESTG00000013213 ENSESTT00000033170 Transcript intron_variant - - - - - - rs8025055 15:68015751 A CCDS10224.1 CCDS10224.1 Transcript intron_variant - - - - - - rs8025055 15:68015751 A ENSESTG00000013213 ENSESTT00000033180 Transcript intron_variant - - - - - - rs8025055 15:68015751 A ENSESTG00000013213 ENSESTT00000033176 Transcript intron_variant - - - - - - rs8025055 15:68015751 A 5607 NM_001206804.1 Transcript intron_variant - - - - - - rs8025055 15:68015751 A 5607 NM_002757.3 Transcript intron_variant - - - - - - rs8025055 15:68015751 A 5607 NM_145160.2 Transcript intron_variant - - - - - - rs8025055 15:68015751 A CCDS55970.1 CCDS55970.1 Transcript intron_variant - - - - - - rs8025055 15:68015751 A ENSESTG00000013213 ENSESTT00000033188 Transcript intron_variant - - - - - - rs12592140 15:68140437 G - - - intergenic_variant - - - - - - rs338341 15:68203476 T - - - intergenic_variant - - - - - - rs392568 15:68232544 A - ENSR00000410234 RegulatoryFeature regulatory_region_variant - - - - - - rs392568 15:68232544 A - - - intergenic_variant - - - - - - rs4777013 15:68251181 G - - - intergenic_variant - - - - - - rs7402733 15:68300773 A - - - intergenic_variant - - - - - - rs12595698 15:68305918 C - - - intergenic_variant - - - - - - rs8024496 15:68310590 C - ENSR00000410249 RegulatoryFeature regulatory_region_variant - - - - - - rs8024496 15:68310590 C - - - intergenic_variant - - - - - - rs11855475 15:68346549 C - ENSR00000410253 RegulatoryFeature regulatory_region_variant - - - - - - rs11855475 15:68346549 C CCDS45290.1 CCDS45290.1 Transcript upstream_gene_variant - - - - - - DISTANCE=116 rs11855475 15:68346549 C ENSESTG00000013248 ENSESTT00000033263 Transcript upstream_gene_variant - - - - - - DISTANCE=107 rs11855475 15:68346549 C 8554 NM_016166.1 Transcript upstream_gene_variant - - - - - - DISTANCE=23 rs11855475 15:68346549 C ENSESTG00000013248 ENSESTT00000033256 Transcript upstream_gene_variant - - - - - - DISTANCE=107 rs12911030 15:68383873 C CCDS45290.1 CCDS45290.1 Transcript intron_variant - - - - - - rs12911030 15:68383873 C ENSESTG00000013248 ENSESTT00000033263 Transcript intron_variant - - - - - - rs12911030 15:68383873 C 8554 NM_016166.1 Transcript intron_variant - - - - - - rs12911030 15:68383873 C ENSESTG00000013248 ENSESTT00000033256 Transcript intron_variant - - - - - - rs6416489 15:68405134 G CCDS45290.1 CCDS45290.1 Transcript intron_variant - - - - - - rs6416489 15:68405134 G ENSESTG00000013248 ENSESTT00000033263 Transcript intron_variant - - - - - - rs6416489 15:68405134 G 8554 NM_016166.1 Transcript intron_variant - - - - - - rs6416489 15:68405134 G ENSESTG00000013248 ENSESTT00000033256 Transcript intron_variant - - - - - - rs6494716 15:68419232 G CCDS45290.1 CCDS45290.1 Transcript intron_variant - - - - - - rs6494716 15:68419232 G ENSESTG00000013248 ENSESTT00000033263 Transcript intron_variant - - - - - - rs6494716 15:68419232 G 8554 NM_016166.1 Transcript intron_variant - - - - - - rs6494716 15:68419232 G ENSESTG00000013248 ENSESTT00000033256 Transcript intron_variant - - - - - - rs7180355 15:68419676 C CCDS45290.1 CCDS45290.1 Transcript intron_variant - - - - - - rs7180355 15:68419676 C ENSESTG00000013248 ENSESTT00000033263 Transcript intron_variant - - - - - - rs7180355 15:68419676 C 8554 NM_016166.1 Transcript intron_variant - - - - - - rs7180355 15:68419676 C ENSESTG00000013248 ENSESTT00000033256 Transcript intron_variant - - - - - - rs7183205 15:68498268 G - ENSR00000410271 RegulatoryFeature regulatory_region_variant - - - - - - rs7183205 15:68498268 G 91860 NM_001031733.2 Transcript 5_prime_UTR_variant 181 - - - - - rs7183205 15:68498268 G ENSESTG00000013307 ENSESTT00000033406 Transcript downstream_gene_variant - - - - - - DISTANCE=2461 rs7183205 15:68498268 G ENSESTG00000013307 ENSESTT00000033398 Transcript downstream_gene_variant - - - - - - DISTANCE=2124 rs7183205 15:68498268 G ENSESTG00000013307 ENSESTT00000033392 Transcript downstream_gene_variant - - - - - - DISTANCE=2397 rs7183205 15:68498268 G ENSESTG00000013326 ENSESTT00000033429 Transcript upstream_gene_variant - - - - - - DISTANCE=600 rs7183205 15:68498268 G 91860 NM_033429.2 Transcript 5_prime_UTR_variant 181 - - - - - rs7183205 15:68498268 G CCDS42052.1 CCDS42052.1 Transcript upstream_gene_variant - - - - - - DISTANCE=554 rs7183205 15:68498268 G 54982 NM_017882.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1062 rs7183205 15:68498268 G ENSESTG00000013307 ENSESTT00000033388 Transcript downstream_gene_variant - - - - - - DISTANCE=2299 rs7183205 15:68498268 G CCDS10227.1 CCDS10227.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2210 rs7183205 15:68498268 G CCDS10226.2 CCDS10226.2 Transcript upstream_gene_variant - - - - - - DISTANCE=554 rs4777026 15:68506157 C ENSESTG00000013307 ENSESTT00000033406 Transcript intron_variant - - - - - - rs4777026 15:68506157 C ENSESTG00000013307 ENSESTT00000033398 Transcript intron_variant - - - - - - rs4777026 15:68506157 C ENSESTG00000013307 ENSESTT00000033411 Transcript downstream_gene_variant - - - - - - DISTANCE=426 rs4777026 15:68506157 C ENSESTG00000013307 ENSESTT00000033392 Transcript intron_variant - - - - - - rs4777026 15:68506157 C ENSESTG00000013307 ENSESTT00000033366 Transcript downstream_gene_variant - - - - - - DISTANCE=4778 rs4777026 15:68506157 C 54982 NM_017882.2 Transcript intron_variant - - - - - - rs4777026 15:68506157 C ENSESTG00000013307 ENSESTT00000033388 Transcript intron_variant - - - - - - rs4777026 15:68506157 C CCDS10227.1 CCDS10227.1 Transcript intron_variant - - - - - - rs4777026 15:68506157 C ENSESTG00000013307 ENSESTT00000033404 Transcript intron_variant - - - - - - rs4777026 15:68506157 C ENSESTG00000013307 ENSESTT00000033409 Transcript downstream_gene_variant - - - - - - DISTANCE=3594 rs6494723 15:68532547 C ENSESTG00000013307 ENSESTT00000033366 Transcript intron_variant - - - - - - rs7177709 15:68637787 C 22801 NM_001004439.1 Transcript intron_variant - - - - - - rs7177709 15:68637787 C ENSESTG00000013285 ENSESTT00000033305 Transcript intron_variant - - - - - - rs7177709 15:68637787 C ENSESTG00000013287 ENSESTT00000033323 Transcript intron_variant - - - - - - rs7177709 15:68637787 C CCDS45291.1 CCDS45291.1 Transcript intron_variant - - - - - - rs2415004 15:68659946 T 22801 NM_001004439.1 Transcript intron_variant - - - - - - rs2415004 15:68659946 T ENSESTG00000013285 ENSESTT00000033305 Transcript upstream_gene_variant - - - - - - DISTANCE=1153 rs2415004 15:68659946 T CCDS45291.1 CCDS45291.1 Transcript intron_variant - - - - - - rs2415004 15:68659946 T ENSESTG00000013277 ENSESTT00000033304 Transcript intron_variant - - - - - - rs967564 15:68665596 G 22801 NM_001004439.1 Transcript intron_variant - - - - - - rs967564 15:68665596 G CCDS45291.1 CCDS45291.1 Transcript intron_variant - - - - - - rs967564 15:68665596 G ENSESTG00000013277 ENSESTT00000033304 Transcript intron_variant - - - - - - rs4462541 15:68934153 C 10391 NM_001190456.1 Transcript intron_variant - - - - - - rs4462541 15:68934153 C ENSESTG00000030452 ENSESTT00000076778 Transcript intron_variant - - - - - - rs4462541 15:68934153 C CCDS53952.1 CCDS53952.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3346 rs4462541 15:68934153 C 10391 NM_001190457.1 Transcript intron_variant - - - - - - rs4462541 15:68934153 C ENSESTG00000030452 ENSESTT00000076810 Transcript intron_variant - - - - - - rs4462541 15:68934153 C ENSESTG00000030452 ENSESTT00000076821 Transcript intron_variant - - - - - - rs4462541 15:68934153 C CCDS10229.2 CCDS10229.2 Transcript intron_variant - - - - - - rs4462541 15:68934153 C ENSESTG00000030452 ENSESTT00000076868 Transcript intron_variant - - - - - - rs4462541 15:68934153 C ENSESTG00000030452 ENSESTT00000076751 Transcript intron_variant - - - - - - rs4462541 15:68934153 C ENSESTG00000030452 ENSESTT00000076796 Transcript intron_variant - - - - - - rs4462541 15:68934153 C 10391 NM_006091.4 Transcript intron_variant - - - - - - rs4462541 15:68934153 C ENSESTG00000030452 ENSESTT00000076854 Transcript intron_variant - - - - - - rs4776414 15:68942861 G 10391 NM_001190456.1 Transcript intron_variant - - - - - - rs4776414 15:68942861 G ENSESTG00000030452 ENSESTT00000076778 Transcript intron_variant - - - - - - rs4776414 15:68942861 G CCDS53952.1 CCDS53952.1 Transcript intron_variant - - - - - - rs4776414 15:68942861 G 10391 NM_001190457.1 Transcript intron_variant - - - - - - rs4776414 15:68942861 G ENSESTG00000030452 ENSESTT00000076810 Transcript intron_variant - - - - - - rs4776414 15:68942861 G ENSESTG00000030452 ENSESTT00000076821 Transcript intron_variant - - - - - - rs4776414 15:68942861 G CCDS10229.2 CCDS10229.2 Transcript intron_variant - - - - - - rs4776414 15:68942861 G ENSESTG00000030452 ENSESTT00000076868 Transcript intron_variant - - - - - - rs4776414 15:68942861 G ENSESTG00000030452 ENSESTT00000076751 Transcript intron_variant - - - - - - rs4776414 15:68942861 G ENSESTG00000030452 ENSESTT00000076796 Transcript intron_variant - - - - - - rs4776414 15:68942861 G 10391 NM_006091.4 Transcript intron_variant - - - - - - rs4776414 15:68942861 G ENSESTG00000030452 ENSESTT00000076854 Transcript intron_variant - - - - - - rs12050864 15:69023498 A 10391 NM_001190456.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3353 rs12050864 15:69023498 A ENSESTG00000030452 ENSESTT00000076778 Transcript downstream_gene_variant - - - - - - DISTANCE=4661 rs12050864 15:69023498 A 10391 NM_001190457.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3353 rs12050864 15:69023498 A ENSESTG00000030452 ENSESTT00000076810 Transcript downstream_gene_variant - - - - - - DISTANCE=4661 rs12050864 15:69023498 A ENSESTG00000030452 ENSESTT00000076821 Transcript downstream_gene_variant - - - - - - DISTANCE=4661 rs12050864 15:69023498 A ENSESTG00000030452 ENSESTT00000076868 Transcript downstream_gene_variant - - - - - - DISTANCE=4661 rs12050864 15:69023498 A ENSESTG00000030452 ENSESTT00000076751 Transcript downstream_gene_variant - - - - - - DISTANCE=4661 rs12050864 15:69023498 A ENSESTG00000030452 ENSESTT00000076796 Transcript downstream_gene_variant - - - - - - DISTANCE=4661 rs12050864 15:69023498 A 10391 NM_006091.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3353 rs12050864 15:69023498 A ENSESTG00000030452 ENSESTT00000076854 Transcript downstream_gene_variant - - - - - - DISTANCE=4661 rs7179370 15:69078562 C ENSESTG00000030673 ENSESTT00000077247 Transcript intron_variant - - - - - - rs7179370 15:69078562 C CCDS45292.1 CCDS45292.1 Transcript intron_variant - - - - - - rs7179370 15:69078562 C 8125 NM_006305.3 Transcript intron_variant - - - - - - rs11855288 15:69972626 G - - - intergenic_variant - - - - - - rs2415067 15:70250463 T - - - intergenic_variant - - - - - - rs4291868 15:70516517 C - - - intergenic_variant - - - - - - rs8182009 15:70518637 C - - - intergenic_variant - - - - - - rs12050522 15:71177087 G ENSESTG00000011551 ENSESTT00000028964 Transcript intron_variant - - - - - - rs12050522 15:71177087 G ENSESTG00000011430 ENSESTT00000028698 Transcript intron_variant - - - - - - rs12050522 15:71177087 G CCDS10237.1 CCDS10237.1 Transcript intron_variant - - - - - - rs12050522 15:71177087 G 56906 NM_020147.3 Transcript intron_variant - - - - - - rs4776540 15:71508598 A ENSESTG00000011533 ENSESTT00000028924 Transcript downstream_gene_variant - - - - - - DISTANCE=954 rs4776540 15:71508598 A CCDS10238.2 CCDS10238.2 Transcript intron_variant - - - - - - rs4776540 15:71508598 A 79875 NM_024817.2 Transcript intron_variant - - - - - - rs4776540 15:71508598 A ENSESTG00000011533 ENSESTT00000028921 Transcript downstream_gene_variant - - - - - - DISTANCE=1021 rs4776540 15:71508598 A ENSESTG00000011533 ENSESTT00000028919 Transcript downstream_gene_variant - - - - - - DISTANCE=1097 rs4287519 15:71767391 T CCDS10238.2 CCDS10238.2 Transcript intron_variant - - - - - - rs4287519 15:71767391 T 79875 NM_024817.2 Transcript intron_variant - - - - - - rs6494970 15:72098922 G - ENSR00000410910 RegulatoryFeature regulatory_region_variant - - - - - - rs6494970 15:72098922 G 10002 NM_016346.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3972 rs6494970 15:72098922 G ENSESTG00000020352 ENSESTT00000051046 Transcript upstream_gene_variant - - - - - - DISTANCE=3984 rs6494970 15:72098922 G 10002 NM_014249.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3972 rs2035378 15:72321031 C ENSESTG00000020702 ENSESTT00000051939 Transcript intron_variant - - - - - - rs2035378 15:72321031 C CCDS10239.1 CCDS10239.1 Transcript intron_variant - - - - - - rs2035378 15:72321031 C ENSESTG00000020702 ENSESTT00000051911 Transcript intron_variant - - - - - - rs2035378 15:72321031 C 4649 NM_006901.3 Transcript intron_variant - - - - - - rs4238452 15:72567404 G ENSESTG00000020551 ENSESTT00000051543 Transcript intron_variant - - - - - - rs4238452 15:72567404 G 56965 NM_020214.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3776 rs8030376 15:72570559 C ENSESTG00000020551 ENSESTT00000051543 Transcript intron_variant - - - - - - rs4625684 15:72598701 G 60677 NM_052840.4 Transcript intron_variant - - - - - - rs4625684 15:72598701 G 60677 NM_001172685.1 Transcript upstream_gene_variant - - - - - - DISTANCE=45 rs4625684 15:72598701 G CCDS10242.1 CCDS10242.1 Transcript intron_variant - - - - - - rs4625684 15:72598701 G CCDS53955.1 CCDS53955.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1566 rs4625684 15:72598701 G 60677 NM_001172684.1 Transcript intron_variant - - - - - - rs4625684 15:72598701 G CCDS53956.1 CCDS53956.1 Transcript intron_variant - - - - - - rs4625684 15:72598701 G ENSESTG00000020523 ENSESTT00000051465 Transcript intron_variant - - - - - - rs4625684 15:72598701 G ENSESTG00000020523 ENSESTT00000051487 Transcript intron_variant - - - - - - rs4470105 15:72656832 C ENSESTG00000020418 ENSESTT00000051199 Transcript intron_variant - - - - - - rs4470105 15:72656832 C CCDS10243.1 CCDS10243.1 Transcript intron_variant - - - - - - rs4470105 15:72656832 C ENSESTG00000020429 ENSESTT00000051365 Transcript intron_variant - - - - - - rs4470105 15:72656832 C 3073 NM_000520.4 Transcript intron_variant - - - - - - rs4470105 15:72656832 C ENSESTG00000020429 ENSESTT00000051418 Transcript intron_variant - - - - - - rs4508386 15:72675700 C ENSESTG00000020418 ENSESTT00000051199 Transcript intron_variant - - - - - - rs4508386 15:72675700 C 80072 NR_027262.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4571 rs4777518 15:72882087 T 693215 NR_030359.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2433 rs4777518 15:72882087 T 25820 NM_005744.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3191 rs11632382 15:73023207 C 585 NM_001252678.1 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013714 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013726 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013721 Transcript intron_variant - - - - - - rs11632382 15:73023207 C 585 NR_045566.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11632382 15:73023207 C 585 NM_033028.4 Transcript intron_variant - - - - - - rs11632382 15:73023207 C CCDS10246.1 CCDS10246.1 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013720 Transcript intron_variant - - - - - - rs11632382 15:73023207 C CCDS58377.1 CCDS58377.1 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013716 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013728 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013705 Transcript intron_variant - - - - - - rs11632382 15:73023207 C 585 NR_045565.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013725 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013711 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013688 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013692 Transcript intron_variant - - - - - - rs11632382 15:73023207 C ENSESTG00000005360 ENSESTT00000013729 Transcript intron_variant - - - - - - rs3862413 15:73086852 C 100287559 NR_040107.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4777579 15:73304879 A - - - intergenic_variant - - - - - - rs2059560 15:73678138 A - - - intergenic_variant - - - - - - rs1280334 15:73764329 G 283677 NM_001042367.1 Transcript intron_variant - - - - - - rs1280334 15:73764329 G CCDS45296.1 CCDS45296.1 Transcript intron_variant - - - - - - rs1280334 15:73764329 G ENSESTG00000006864 ENSESTT00000017470 Transcript intron_variant - - - - - - rs1382422 15:74020049 G - ENSR00000411126 RegulatoryFeature regulatory_region_variant - - - - - - rs1382422 15:74020049 G - - - intergenic_variant - - - - - - rs6495078 15:74055777 C ENSESTG00000007018 ENSESTT00000017784 Transcript upstream_gene_variant - - - - - - DISTANCE=4778 rs4243037 15:74212297 C 100287616 NR_040070.1 Transcript splice_region_variant,intron_variant,nc_transcript_variant - - - - - - rs4243037 15:74212297 C 100287616 NR_040067.1 Transcript splice_region_variant,intron_variant,nc_transcript_variant - - - - - - rs4243037 15:74212297 C 100287616 NR_040066.1 Transcript non_coding_exon_variant,nc_transcript_variant 452 - - - - - rs4243037 15:74212297 C 100287616 NR_040068.1 Transcript non_coding_exon_variant,nc_transcript_variant 267 - - - - - rs4243037 15:74212297 C 100287616 NR_040069.1 Transcript splice_region_variant,intron_variant,nc_transcript_variant - - - - - - rs4243038 15:74212419 G 100287616 NR_040070.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4243038 15:74212419 G 100287616 NR_040067.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4243038 15:74212419 G 100287616 NR_040066.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4243038 15:74212419 G 100287616 NR_040068.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4243038 15:74212419 G 100287616 NR_040069.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8042181 15:74234171 G ENSESTG00000007066 ENSESTT00000017927 Transcript upstream_gene_variant - - - - - - DISTANCE=4538 rs8042181 15:74234171 G CCDS10253.1 CCDS10253.1 Transcript intron_variant - - - - - - rs8042181 15:74234171 G ENSESTG00000007066 ENSESTT00000017923 Transcript upstream_gene_variant - - - - - - DISTANCE=1023 rs8042181 15:74234171 G ENSESTG00000007066 ENSESTT00000017912 Transcript intron_variant - - - - - - rs8042181 15:74234171 G 4016 NM_005576.2 Transcript intron_variant - - - - - - rs4261481 15:74267777 C - - - intergenic_variant - - - - - - rs351182 15:74599355 C - ENSR00001453828 RegulatoryFeature regulatory_region_variant - - - - - - rs351182 15:74599355 C CCDS42058.1 CCDS42058.1 Transcript intron_variant - - - - - - rs351182 15:74599355 C ENSESTG00000007322 ENSESTT00000018442 Transcript downstream_gene_variant - - - - - - DISTANCE=2694 rs351182 15:74599355 C ENSESTG00000007310 ENSESTT00000018428 Transcript downstream_gene_variant - - - - - - DISTANCE=2487 rs351182 15:74599355 C 80125 NM_025055.3 Transcript intron_variant - - - - - - rs351182 15:74599355 C ENSESTG00000007310 ENSESTT00000018432 Transcript downstream_gene_variant - - - - - - DISTANCE=2489 rs2930294 15:74601411 C CCDS42058.1 CCDS42058.1 Transcript intron_variant - - - - - - rs2930294 15:74601411 C ENSESTG00000007322 ENSESTT00000018442 Transcript downstream_gene_variant - - - - - - DISTANCE=4750 rs2930294 15:74601411 C ENSESTG00000007310 ENSESTT00000018428 Transcript downstream_gene_variant - - - - - - DISTANCE=4543 rs2930294 15:74601411 C 80125 NM_025055.3 Transcript intron_variant - - - - - - rs2930294 15:74601411 C ENSESTG00000007310 ENSESTT00000018432 Transcript downstream_gene_variant - - - - - - DISTANCE=4545 rs11072503 15:75052895 C - ENSR00000411333 RegulatoryFeature regulatory_region_variant - - - - - - rs11072503 15:75052895 C 1544 NM_000761.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3954 rs4886637 15:75196428 C CCDS32295.1 CCDS32295.1 Transcript intron_variant - - - - - - rs4886637 15:75196428 C ENSESTG00000032475 ENSESTT00000081964 Transcript downstream_gene_variant - - - - - - DISTANCE=3462 rs4886637 15:75196428 C ENSESTG00000018180 ENSESTT00000045925 Transcript intron_variant - - - - - - rs4886637 15:75196428 C ENSESTG00000018180 ENSESTT00000045904 Transcript intron_variant - - - - - - rs4886637 15:75196428 C ENSESTG00000018180 ENSESTT00000045843 Transcript intron_variant - - - - - - rs4886637 15:75196428 C 57184 NM_020447.3 Transcript intron_variant - - - - - - rs4886637 15:75196428 C ENSESTG00000018180 ENSESTT00000045853 Transcript intron_variant - - - - - - rs11630777 15:75244347 G - ENSR00000411381 RegulatoryFeature regulatory_region_variant - - - - - - rs11630777 15:75244347 G 54913 NM_017793.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3096 rs11630777 15:75244347 G CCDS10274.1 CCDS10274.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3978 rs12904261 15:75780949 C 5780 NM_002833.2 Transcript intron_variant - - - - - - rs12904261 15:75780949 C ENSESTG00000031972 ENSESTT00000081087 Transcript intron_variant - - - - - - rs12904261 15:75780949 C ENSESTG00000031972 ENSESTT00000081072 Transcript intron_variant - - - - - - rs12904261 15:75780949 C ENSESTG00000031972 ENSESTT00000081050 Transcript intron_variant - - - - - - rs12904261 15:75780949 C ENSESTG00000031972 ENSESTT00000081064 Transcript intron_variant - - - - - - rs12904261 15:75780949 C ENSESTG00000031972 ENSESTT00000081041 Transcript intron_variant - - - - - - rs12904261 15:75780949 C ENSESTG00000031972 ENSESTT00000081019 Transcript intron_variant - - - - - - rs12904261 15:75780949 C CCDS10280.1 CCDS10280.1 Transcript intron_variant - - - - - - rs12904261 15:75780949 C ENSESTG00000031972 ENSESTT00000081082 Transcript intron_variant - - - - - - rs12904261 15:75780949 C ENSESTG00000031972 ENSESTT00000080888 Transcript intron_variant - - - - - - rs4886451 15:75912109 T ENSESTG00000031972 ENSESTT00000081050 Transcript intron_variant - - - - - - rs4886451 15:75912109 T 10073 NM_005701.3 Transcript intron_variant - - - - - - rs4886451 15:75912109 T ENSESTG00000031972 ENSESTT00000081041 Transcript intron_variant - - - - - - rs4886451 15:75912109 T ENSESTG00000031972 ENSESTT00000081019 Transcript intron_variant - - - - - - rs4886451 15:75912109 T CCDS10281.1 CCDS10281.1 Transcript intron_variant - - - - - - rs4886451 15:75912109 T ENSESTG00000031972 ENSESTT00000080888 Transcript intron_variant - - - - - - rs4886451 15:75912109 T 10073 NM_001042588.1 Transcript intron_variant - - - - - - rs4886451 15:75912109 T ENSESTG00000030550 ENSESTT00000076910 Transcript intron_variant - - - - - - rs4886451 15:75912109 T ENSESTG00000031972 ENSESTT00000081028 Transcript intron_variant - - - - - - rs4886451 15:75912109 T 10073 NM_001042581.1 Transcript intron_variant - - - - - - rs11634648 15:76486417 T - ENSR00000651045 RegulatoryFeature regulatory_region_variant - - - - - - rs11634648 15:76486417 T 123591 NM_152335.2 Transcript intron_variant - - - - - - rs11634648 15:76486417 T ENSESTG00000031153 ENSESTT00000078576 Transcript intron_variant - - - - - - rs11634648 15:76486417 T ENSESTG00000031153 ENSESTT00000078588 Transcript intron_variant - - - - - - rs11634648 15:76486417 T CCDS10289.2 CCDS10289.2 Transcript intron_variant - - - - - - rs508756 15:76752280 G ENSESTG00000018693 ENSESTT00000047402 Transcript intron_variant - - - - - - rs508756 15:76752280 G ENSESTG00000018693 ENSESTT00000047358 Transcript intron_variant - - - - - - rs508756 15:76752280 G ENSESTG00000018693 ENSESTT00000047376 Transcript intron_variant - - - - - - rs508756 15:76752280 G ENSESTG00000018693 ENSESTT00000047390 Transcript intron_variant - - - - - - rs508756 15:76752280 G 49855 NM_001145923.1 Transcript intron_variant - - - - - - rs508756 15:76752280 G CCDS53962.1 CCDS53962.1 Transcript intron_variant - - - - - - rs508756 15:76752280 G CCDS53961.1 CCDS53961.1 Transcript intron_variant - - - - - - rs508756 15:76752280 G 49855 NM_020843.2 Transcript intron_variant - - - - - - rs157785 15:76811114 G ENSESTG00000018693 ENSESTT00000047370 Transcript intron_variant - - - - - - rs157785 15:76811114 G ENSESTG00000018693 ENSESTT00000047358 Transcript intron_variant - - - - - - rs157785 15:76811114 G ENSESTG00000018693 ENSESTT00000047376 Transcript intron_variant - - - - - - rs157785 15:76811114 G ENSESTG00000018693 ENSESTT00000047390 Transcript intron_variant - - - - - - rs157785 15:76811114 G 49855 NM_001145923.1 Transcript intron_variant - - - - - - rs157785 15:76811114 G ENSESTG00000018693 ENSESTT00000047377 Transcript intron_variant - - - - - - rs157785 15:76811114 G CCDS53962.1 CCDS53962.1 Transcript intron_variant - - - - - - rs157785 15:76811114 G CCDS53961.1 CCDS53961.1 Transcript intron_variant - - - - - - rs157785 15:76811114 G 49855 NM_020843.2 Transcript intron_variant - - - - - - rs280018 15:76967627 G - ENSR00000411640 RegulatoryFeature regulatory_region_variant - - - - - - rs280018 15:76967627 G ENSESTG00000018693 ENSESTT00000047370 Transcript intron_variant - - - - - - rs280018 15:76967627 G ENSESTG00000018693 ENSESTT00000047358 Transcript intron_variant - - - - - - rs280018 15:76967627 G ENSESTG00000018693 ENSESTT00000047376 Transcript intron_variant - - - - - - rs280018 15:76967627 G ENSESTG00000018693 ENSESTT00000047390 Transcript intron_variant - - - - - - rs280018 15:76967627 G 49855 NM_001145923.1 Transcript intron_variant - - - - - - rs280018 15:76967627 G ENSESTG00000018693 ENSESTT00000047377 Transcript intron_variant - - - - - - rs280018 15:76967627 G CCDS53962.1 CCDS53962.1 Transcript intron_variant - - - - - - rs280018 15:76967627 G CCDS53961.1 CCDS53961.1 Transcript intron_variant - - - - - - rs280018 15:76967627 G 49855 NM_020843.2 Transcript intron_variant - - - - - - rs57228545 15:77275163 T - - - intergenic_variant - - - - - - rs2667786 15:77804888 T - - - intergenic_variant - - - - - - rs12905721 15:77885333 T - ENSR00000651059 RegulatoryFeature regulatory_region_variant - - - - - - rs12905721 15:77885333 T - - - intergenic_variant - - - - - - rs10444810 15:78318272 G CCDS32301.2 CCDS32301.2 Transcript intron_variant - - - - - - rs10444810 15:78318272 G ENSESTG00000007537 ENSESTT00000019015 Transcript intron_variant - - - - - - rs10444810 15:78318272 G 23102 NM_015079.5 Transcript intron_variant - - - - - - rs10444810 15:78318272 G ENSESTG00000007555 ENSESTT00000019044 Transcript upstream_gene_variant - - - - - - DISTANCE=1534 rs10444810 15:78318272 G ENSESTG00000007537 ENSESTT00000019001 Transcript intron_variant - - - - - - rs10444810 15:78318272 G CCDS45314.1 CCDS45314.1 Transcript intron_variant - - - - - - rs10444810 15:78318272 G 23102 NM_144572.1 Transcript intron_variant - - - - - - rs2028547 15:78333587 T CCDS32301.2 CCDS32301.2 Transcript intron_variant - - - - - - rs2028547 15:78333587 T ENSESTG00000007537 ENSESTT00000019015 Transcript intron_variant - - - - - - rs2028547 15:78333587 T ENSESTG00000007537 ENSESTT00000019013 Transcript intron_variant - - - - - - rs2028547 15:78333587 T 23102 NM_015079.5 Transcript intron_variant - - - - - - rs2028547 15:78333587 T ENSESTG00000007537 ENSESTT00000019001 Transcript intron_variant - - - - - - rs2028547 15:78333587 T CCDS45314.1 CCDS45314.1 Transcript intron_variant - - - - - - rs2028547 15:78333587 T 23102 NM_144572.1 Transcript intron_variant - - - - - - rs1992469 15:78403004 G CCDS10296.1 CCDS10296.1 Transcript intron_variant - - - - - - rs1992469 15:78403004 G ENSESTG00000007517 ENSESTT00000018959 Transcript intron_variant - - - - - - rs1992469 15:78403004 G ENSESTG00000007517 ENSESTT00000018941 Transcript intron_variant - - - - - - rs1992469 15:78403004 G 10518 NM_006383.2 Transcript intron_variant - - - - - - rs1992469 15:78403004 G ENSESTG00000007517 ENSESTT00000018969 Transcript intron_variant - - - - - - rs2868606 15:78471320 G 23205 NM_015162.4 Transcript intron_variant - - - - - - rs2868606 15:78471320 G ENSESTG00000007495 ENSESTT00000018911 Transcript intron_variant - - - - - - rs2868606 15:78471320 G ENSESTG00000007463 ENSESTT00000018836 Transcript downstream_gene_variant - - - - - - DISTANCE=3108 rs2868606 15:78471320 G CCDS10298.1 CCDS10298.1 Transcript intron_variant - - - - - - rs2868606 15:78471320 G 23205 NM_001199377.1 Transcript intron_variant - - - - - - rs2868606 15:78471320 G ENSESTG00000007495 ENSESTT00000018919 Transcript upstream_gene_variant - - - - - - DISTANCE=202 rs2868606 15:78471320 G ENSESTG00000007463 ENSESTT00000018867 Transcript downstream_gene_variant - - - - - - DISTANCE=3108 rs1040263 15:78509634 C - ENSR00000411869 RegulatoryFeature regulatory_region_variant - - - - - - rs1040263 15:78509634 C ENSESTG00000007463 ENSESTT00000018855 Transcript intron_variant - - - - - - rs1040263 15:78509634 C ENSESTG00000007463 ENSESTT00000018842 Transcript intron_variant - - - - - - rs1040263 15:78509634 C 23205 NM_015162.4 Transcript intron_variant - - - - - - rs1040263 15:78509634 C ENSESTG00000007463 ENSESTT00000018836 Transcript intron_variant - - - - - - rs1040263 15:78509634 C CCDS10298.1 CCDS10298.1 Transcript intron_variant - - - - - - rs1040263 15:78509634 C 23205 NM_001199377.1 Transcript intron_variant - - - - - - rs4243080 15:78680263 C - ENSR00000411895 RegulatoryFeature regulatory_region_variant - - - - - - rs4243080 15:78680263 C - - - intergenic_variant - - - - - - rs2656061 15:78726297 C 3658 NM_004136.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4221 rs2656061 15:78726297 C ENSESTG00000000276 ENSESTT00000000685 Transcript upstream_gene_variant - - - - - - DISTANCE=4239 rs2656061 15:78726297 C CCDS10302.1 CCDS10302.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4383 rs602070 15:78877330 C 1138 NM_000745.3 Transcript intron_variant - - - - - - rs602070 15:78877330 C ENSESTG00000000315 ENSESTT00000000784 Transcript intron_variant - - - - - - rs602070 15:78877330 C ENSESTG00000000315 ENSESTT00000000779 Transcript intron_variant - - - - - - rs602070 15:78877330 C CCDS10304.1 CCDS10304.1 Transcript intron_variant - - - - - - rs602070 15:78877330 C ENSESTG00000000315 ENSESTT00000000781 Transcript intron_variant - - - - - - rs602070 15:78877330 C ENSESTG00000000315 ENSESTT00000000783 Transcript intron_variant - - - - - - rs12708525 15:79383260 C - ENSR00000411979 RegulatoryFeature regulatory_region_variant - - - - - - rs12708525 15:79383260 C CCDS45320.1 CCDS45320.1 Transcript upstream_gene_variant - - - - - - DISTANCE=420 rs12708525 15:79383260 C 5923 NM_002891.4 Transcript upstream_gene_variant - - - - - - DISTANCE=45 rs12708525 15:79383260 C CCDS10309.1 CCDS10309.1 Transcript upstream_gene_variant - - - - - - DISTANCE=420 rs12708525 15:79383260 C 5923 NM_001145648.1 Transcript upstream_gene_variant - - - - - - DISTANCE=45 rs1434461 15:79515616 G ENSESTG00000000354 ENSESTT00000000925 Transcript intron_variant - - - - - - rs1434461 15:79515616 G ENSESTG00000000354 ENSESTT00000000920 Transcript intron_variant - - - - - - rs1434461 15:79515616 G 729911 NR_038997.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1434461 15:79515616 G ENSESTG00000000354 ENSESTT00000000916 Transcript intron_variant - - - - - - rs8035164 15:79693020 A ENSESTG00000000345 ENSESTT00000000894 Transcript intron_variant - - - - - - rs2586159 15:80281956 C - - - intergenic_variant - - - - - - rs7359273 15:80283282 T - - - intergenic_variant - - - - - - rs2461650 15:80290135 G - - - intergenic_variant - - - - - - rs6495475 15:80420062 G ENSESTG00000013969 ENSESTT00000035000 Transcript intron_variant - - - - - - rs6495475 15:80420062 G ENSESTG00000013969 ENSESTT00000034998 Transcript intron_variant - - - - - - rs6495475 15:80420062 G 54469 NM_001242911.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G 54469 NM_001242913.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G ENSESTG00000013969 ENSESTT00000034986 Transcript intron_variant - - - - - - rs6495475 15:80420062 G 54469 NM_001242916.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G 54469 NM_019006.3 Transcript intron_variant - - - - - - rs6495475 15:80420062 G 54469 NM_001242918.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G CCDS58395.1 CCDS58395.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G ENSESTG00000013969 ENSESTT00000034955 Transcript intron_variant - - - - - - rs6495475 15:80420062 G ENSESTG00000013969 ENSESTT00000034970 Transcript intron_variant - - - - - - rs6495475 15:80420062 G ENSESTG00000013969 ENSESTT00000034977 Transcript intron_variant - - - - - - rs6495475 15:80420062 G 54469 NM_001242912.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G ENSESTG00000013969 ENSESTT00000034989 Transcript intron_variant - - - - - - rs6495475 15:80420062 G 54469 NM_001242917.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G ENSESTG00000013969 ENSESTT00000035006 Transcript upstream_gene_variant - - - - - - DISTANCE=3424 rs6495475 15:80420062 G 54469 NM_001242915.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G 54469 NM_001242914.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G ENSESTG00000013969 ENSESTT00000034964 Transcript intron_variant - - - - - - rs6495475 15:80420062 G 54469 NM_001242919.1 Transcript intron_variant - - - - - - rs6495475 15:80420062 G CCDS10313.1 CCDS10313.1 Transcript intron_variant - - - - - - rs3905658 15:80638974 G ENSESTG00000004167 ENSESTT00000010510 Transcript intron_variant - - - - - - rs3905658 15:80638974 G 283688 NR_033833.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4827 rs3905658 15:80638974 G ENSESTG00000014059 ENSESTT00000035136 Transcript upstream_gene_variant - - - - - - DISTANCE=4864 rs8035688 15:81103335 C 57214 NM_018689.1 Transcript intron_variant - - - - - - rs8035688 15:81103335 C ENSESTG00000004010 ENSESTT00000010144 Transcript intron_variant - - - - - - rs12440399 15:81189088 T CCDS10315.1 CCDS10315.1 Transcript intron_variant - - - - - - rs12440399 15:81189088 T 57214 NM_018689.1 Transcript intron_variant - - - - - - rs12440399 15:81189088 T ENSESTG00000004161 ENSESTT00000010496 Transcript intron_variant - - - - - - rs12440399 15:81189088 T ENSESTG00000004020 ENSESTT00000010226 Transcript intron_variant - - - - - - rs12440399 15:81189088 T ENSESTG00000004161 ENSESTT00000010493 Transcript intron_variant - - - - - - rs12440399 15:81189088 T ENSESTG00000004020 ENSESTT00000010228 Transcript intron_variant - - - - - - rs1395924 15:81198107 T CCDS10315.1 CCDS10315.1 Transcript intron_variant - - - - - - rs1395924 15:81198107 T 57214 NM_018689.1 Transcript intron_variant - - - - - - rs1395924 15:81198107 T ENSESTG00000004161 ENSESTT00000010496 Transcript intron_variant - - - - - - rs1395924 15:81198107 T ENSESTG00000004020 ENSESTT00000010226 Transcript intron_variant - - - - - - rs1395924 15:81198107 T ENSESTG00000004161 ENSESTT00000010493 Transcript intron_variant - - - - - - rs1395924 15:81198107 T ENSESTG00000004020 ENSESTT00000010228 Transcript intron_variant - - - - - - rs2663942 15:81365699 G - - - intergenic_variant - - - - - - rs2683261 15:81387971 C - - - intergenic_variant - - - - - - rs2663931 15:81412409 T - - - intergenic_variant - - - - - - rs4485315 15:81464754 T - - - intergenic_variant - - - - - - rs6495571 15:81678066 G - - - intergenic_variant - - - - - - rs2672087 15:81808687 C - ENSR00001454380 RegulatoryFeature regulatory_region_variant - - - - - - rs2672087 15:81808687 C - - - intergenic_variant - - - - - - rs10851963 15:82447011 C ENSESTG00000026040 ENSESTT00000065622 Transcript downstream_gene_variant - - - - - - DISTANCE=2304 rs10851963 15:82447011 C 79631 NM_001040610.2 Transcript intron_variant - - - - - - rs10851963 15:82447011 C 79631 NM_024580.5 Transcript intron_variant - - - - - - rs10851963 15:82447011 C ENSESTG00000026220 ENSESTT00000066187 Transcript intron_variant - - - - - - rs10851963 15:82447011 C ENSESTG00000026273 ENSESTT00000066252 Transcript upstream_gene_variant - - - - - - DISTANCE=3000 rs10851963 15:82447011 C CCDS42070.1 CCDS42070.1 Transcript intron_variant - - - - - - rs10851963 15:82447011 C CCDS42071.1 CCDS42071.1 Transcript intron_variant - - - - - - rs2134047 15:82455421 G 79631 NM_001040610.2 Transcript intron_variant - - - - - - rs2134047 15:82455421 G 79631 NM_024580.5 Transcript intron_variant - - - - - - rs2134047 15:82455421 G ENSESTG00000026220 ENSESTT00000066187 Transcript intron_variant - - - - - - rs2134047 15:82455421 G CCDS42070.1 CCDS42070.1 Transcript intron_variant - - - - - - rs2134047 15:82455421 G CCDS42071.1 CCDS42071.1 Transcript intron_variant - - - - - - rs1846909 15:82510932 C 79631 NM_001040610.2 Transcript intron_variant - - - - - - rs1846909 15:82510932 C 79631 NM_024580.5 Transcript intron_variant - - - - - - rs1846909 15:82510932 C ENSESTG00000026220 ENSESTT00000066187 Transcript intron_variant - - - - - - rs1846909 15:82510932 C CCDS42070.1 CCDS42070.1 Transcript intron_variant - - - - - - rs1846909 15:82510932 C CCDS42071.1 CCDS42071.1 Transcript intron_variant - - - - - - rs1267655 15:83220198 C ENSESTG00000004297 ENSESTT00000010877 Transcript intron_variant - - - - - - rs1267655 15:83220198 C 64506 NM_030594.3 Transcript intron_variant - - - - - - rs1267655 15:83220198 C 64506 NM_001079535.1 Transcript intron_variant - - - - - - rs1267655 15:83220198 C ENSESTG00000004297 ENSESTT00000010899 Transcript intron_variant - - - - - - rs1267655 15:83220198 C CCDS42072.1 CCDS42072.1 Transcript intron_variant - - - - - - rs1267655 15:83220198 C 64506 NM_001079533.1 Transcript intron_variant - - - - - - rs1267655 15:83220198 C ENSESTG00000004297 ENSESTT00000010885 Transcript downstream_gene_variant - - - - - - DISTANCE=1030 rs1267655 15:83220198 C ENSESTG00000004297 ENSESTT00000010892 Transcript intron_variant - - - - - - rs1267655 15:83220198 C CCDS45330.1 CCDS45330.1 Transcript intron_variant - - - - - - rs1267655 15:83220198 C ENSESTG00000004297 ENSESTT00000010865 Transcript intron_variant - - - - - - rs1267655 15:83220198 C CCDS45329.1 CCDS45329.1 Transcript intron_variant - - - - - - rs1267655 15:83220198 C ENSESTG00000004297 ENSESTT00000010897 Transcript intron_variant - - - - - - rs1267655 15:83220198 C ENSESTG00000004297 ENSESTT00000010879 Transcript intron_variant - - - - - - rs1267655 15:83220198 C 64506 NM_001079534.1 Transcript intron_variant - - - - - - rs1267655 15:83220198 C ENSESTG00000010015 ENSESTT00000025052 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010900 Transcript intron_variant - - - - - - rs1259181 15:83229871 T 64506 NM_001079535.1 Transcript intron_variant - - - - - - rs1259181 15:83229871 T CCDS42072.1 CCDS42072.1 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010903 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010892 Transcript intron_variant - - - - - - rs1259181 15:83229871 T CCDS45330.1 CCDS45330.1 Transcript intron_variant - - - - - - rs1259181 15:83229871 T CCDS45329.1 CCDS45329.1 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010897 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010879 Transcript intron_variant - - - - - - rs1259181 15:83229871 T 64506 NM_001079534.1 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000010015 ENSESTT00000025052 Transcript intron_variant - - - - - - rs1259181 15:83229871 T 64506 NM_030594.3 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010877 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010895 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010899 Transcript intron_variant - - - - - - rs1259181 15:83229871 T 64506 NM_001079533.1 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010871 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010885 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010865 Transcript intron_variant - - - - - - rs1259181 15:83229871 T ENSESTG00000004297 ENSESTT00000010902 Transcript intron_variant - - - - - - rs1313491 15:83272813 C ENSESTG00000004297 ENSESTT00000010877 Transcript intron_variant - - - - - - rs1313491 15:83272813 C 64506 NM_030594.3 Transcript intron_variant - - - - - - rs1313491 15:83272813 C ENSESTG00000004297 ENSESTT00000010895 Transcript intron_variant - - - - - - rs1313491 15:83272813 C ENSESTG00000004297 ENSESTT00000010885 Transcript intron_variant - - - - - - rs1313491 15:83272813 C ENSESTG00000004297 ENSESTT00000010871 Transcript intron_variant - - - - - - rs1313491 15:83272813 C ENSESTG00000004297 ENSESTT00000010892 Transcript intron_variant - - - - - - rs1313491 15:83272813 C ENSESTG00000004297 ENSESTT00000010865 Transcript intron_variant - - - - - - rs1313491 15:83272813 C CCDS45329.1 CCDS45329.1 Transcript intron_variant - - - - - - rs1313491 15:83272813 C ENSESTG00000004297 ENSESTT00000010879 Transcript intron_variant - - - - - - rs2667390 15:83524512 C - ENSR00000651202 RegulatoryFeature regulatory_region_variant - - - - - - rs2667390 15:83524512 C 9455 NM_199330.2 Transcript intron_variant - - - - - - rs2667390 15:83524512 C CCDS45336.1 CCDS45336.1 Transcript intron_variant - - - - - - rs2667390 15:83524512 C ENSESTG00000004244 ENSESTT00000010697 Transcript intron_variant - - - - - - rs2667390 15:83524512 C 9455 NM_004839.3 Transcript intron_variant - - - - - - rs2667390 15:83524512 C ENSESTG00000004244 ENSESTT00000010701 Transcript intron_variant - - - - - - rs2667390 15:83524512 C ENSESTG00000004244 ENSESTT00000010703 Transcript downstream_gene_variant - - - - - - DISTANCE=3277 rs2667390 15:83524512 C CCDS45334.1 CCDS45334.1 Transcript intron_variant - - - - - - rs3101933 15:83538059 C 9455 NM_199330.2 Transcript intron_variant - - - - - - rs3101933 15:83538059 C CCDS45336.1 CCDS45336.1 Transcript intron_variant - - - - - - rs3101933 15:83538059 C ENSESTG00000004244 ENSESTT00000010697 Transcript intron_variant - - - - - - rs3101933 15:83538059 C 9455 NM_004839.3 Transcript intron_variant - - - - - - rs3101933 15:83538059 C ENSESTG00000004244 ENSESTT00000010701 Transcript intron_variant - - - - - - rs3101933 15:83538059 C ENSESTG00000004244 ENSESTT00000010703 Transcript intron_variant - - - - - - rs3101933 15:83538059 C CCDS45334.1 CCDS45334.1 Transcript intron_variant - - - - - - rs12916616 15:84355371 G CCDS10326.1 CCDS10326.1 Transcript intron_variant - - - - - - rs12916616 15:84355371 G ENSESTG00000035514 ENSESTT00000089694 Transcript intron_variant - - - - - - rs12916616 15:84355371 G 57188 NM_207517.2 Transcript intron_variant - - - - - - rs9672567 15:84951738 G ENSESTG00000027406 ENSESTT00000069013 Transcript intron_variant - - - - - - rs9672567 15:84951738 G ENSESTG00000027418 ENSESTT00000069039 Transcript intron_variant - - - - - - rs9672567 15:84951738 G ENSESTG00000027418 ENSESTT00000069048 Transcript intron_variant - - - - - - rs309426 15:85157391 T CCDS10329.2 CCDS10329.2 Transcript intron_variant - - - - - - rs309426 15:85157391 T ENSESTG00000026529 ENSESTT00000066799 Transcript intron_variant - - - - - - rs309426 15:85157391 T 54993 NM_181877.3 Transcript intron_variant - - - - - - rs309426 15:85157391 T ENSESTG00000027222 ENSESTT00000068581 Transcript intron_variant - - - - - - rs309426 15:85157391 T CCDS32315.1 CCDS32315.1 Transcript intron_variant - - - - - - rs309426 15:85157391 T 54993 NM_001007072.1 Transcript intron_variant - - - - - - rs4842984 15:85162844 T CCDS10329.2 CCDS10329.2 Transcript intron_variant - - - - - - rs4842984 15:85162844 T ENSESTG00000026529 ENSESTT00000066799 Transcript intron_variant - - - - - - rs4842984 15:85162844 T 54993 NM_181877.3 Transcript intron_variant - - - - - - rs4842984 15:85162844 T ENSESTG00000027222 ENSESTT00000068581 Transcript intron_variant - - - - - - rs4842984 15:85162844 T CCDS32315.1 CCDS32315.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3270 rs4842984 15:85162844 T 54993 NM_001007072.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3003 rs695111 15:85168775 C CCDS10329.2 CCDS10329.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3504 rs695111 15:85168775 C ENSESTG00000026529 ENSESTT00000066799 Transcript downstream_gene_variant - - - - - - DISTANCE=1827 rs695111 15:85168775 C ENSESTG00000026543 ENSESTT00000066843 Transcript upstream_gene_variant - - - - - - DISTANCE=1623 rs695111 15:85168775 C 54993 NM_181877.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1828 rs695111 15:85168775 C ENSESTG00000027222 ENSESTT00000068581 Transcript intron_variant - - - - - - rs4842979 15:85244282 C ENSESTG00000027004 ENSESTT00000068218 Transcript intron_variant - - - - - - rs4842979 15:85244282 C CCDS45340.1 CCDS45340.1 Transcript intron_variant - - - - - - rs4842979 15:85244282 C ENSESTG00000027004 ENSESTT00000068197 Transcript intron_variant - - - - - - rs4842979 15:85244282 C ENSESTG00000027004 ENSESTT00000068268 Transcript intron_variant - - - - - - rs4842979 15:85244282 C 23478 NM_014300.2 Transcript intron_variant - - - - - - rs4842979 15:85244282 C ENSESTG00000027004 ENSESTT00000068281 Transcript intron_variant - - - - - - rs4842979 15:85244282 C ENSESTG00000027004 ENSESTT00000068292 Transcript intron_variant - - - - - - rs8025154 15:85295237 C 9640 NM_014630.2 Transcript intron_variant - - - - - - rs386173 15:85407215 T - ENSR00001023441 RegulatoryFeature regulatory_region_variant - - - - - - rs386173 15:85407215 T ENSESTG00000026683 ENSESTT00000067171 Transcript downstream_gene_variant - - - - - - DISTANCE=4705 rs386173 15:85407215 T ENSESTG00000026697 ENSESTT00000067229 Transcript intron_variant - - - - - - rs386173 15:85407215 T CCDS10333.1 CCDS10333.1 Transcript intron_variant - - - - - - rs386173 15:85407215 T 57538 NM_020778.4 Transcript intron_variant - - - - - - rs386173 15:85407215 T ENSESTG00000026697 ENSESTT00000067239 Transcript upstream_gene_variant - - - - - - DISTANCE=374 rs386173 15:85407215 T ENSESTG00000026675 ENSESTT00000067162 Transcript intron_variant - - - - - - rs386173 15:85407215 T ENSESTG00000026697 ENSESTT00000067234 Transcript intron_variant - - - - - - rs4356451 15:85491942 C - ENSR00000412716 RegulatoryFeature regulatory_region_variant - - - - - - rs4356451 15:85491942 C CCDS10334.1 CCDS10334.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3511 rs4356451 15:85491942 C ENSESTG00000026734 ENSESTT00000067483 Transcript intron_variant - - - - - - rs4356451 15:85491942 C ENSESTG00000026734 ENSESTT00000067539 Transcript intron_variant - - - - - - rs4356451 15:85491942 C 9154 NM_004213.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2915 rs11074081 15:85847006 T ENSESTG00000020229 ENSESTT00000050731 Transcript intron_variant - - - - - - rs11854646 15:85932354 G 11214 NM_006738.4 Transcript intron_variant - - - - - - rs11854646 15:85932354 G ENSESTG00000019868 ENSESTT00000049900 Transcript intron_variant - - - - - - rs11854646 15:85932354 G 11214 NM_007200.3 Transcript intron_variant - - - - - - rs6496021 15:86039498 C 11214 NM_006738.4 Transcript intron_variant - - - - - - rs6496021 15:86039498 C ENSESTG00000019868 ENSESTT00000049900 Transcript intron_variant - - - - - - rs6496021 15:86039498 C 11214 NM_007200.3 Transcript intron_variant - - - - - - rs6496021 15:86039498 C CCDS32319.1 CCDS32319.1 Transcript intron_variant - - - - - - rs6496021 15:86039498 C CCDS32320.1 CCDS32320.1 Transcript intron_variant - - - - - - rs12909565 15:86301443 G 64410 NM_022480.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1114 rs2166092 15:86673367 C - - - intergenic_variant - - - - - - rs2437784 15:87109654 C CCDS58398.1 CCDS58398.1 Transcript intron_variant - - - - - - rs2437784 15:87109654 C 123624 NM_152336.2 Transcript intron_variant - - - - - - rs6496348 15:87139733 T CCDS58398.1 CCDS58398.1 Transcript intron_variant - - - - - - rs6496348 15:87139733 T 123624 NM_152336.2 Transcript intron_variant - - - - - - rs2347249 15:87399162 C CCDS58398.1 CCDS58398.1 Transcript intron_variant - - - - - - rs2347249 15:87399162 C 123624 NM_152336.2 Transcript intron_variant - - - - - - rs7171585 15:87413826 G CCDS58398.1 CCDS58398.1 Transcript intron_variant - - - - - - rs7171585 15:87413826 G 123624 NM_152336.2 Transcript intron_variant - - - - - - rs2701374 15:87511298 A CCDS58398.1 CCDS58398.1 Transcript intron_variant - - - - - - rs2701374 15:87511298 A 123624 NM_152336.2 Transcript intron_variant - - - - - - rs2701370 15:87623845 A - ENSR00001454805 RegulatoryFeature regulatory_region_variant - - - - - - rs2701370 15:87623845 A - - - intergenic_variant - - - - - - rs1353879 15:87761433 A - - - intergenic_variant - - - - - - rs4595770 15:88254649 T - ENSR00001454854 RegulatoryFeature regulatory_region_variant - - - - - - rs4595770 15:88254649 T - - - intergenic_variant - - - - - - rs2196306 15:88388984 C - - - intergenic_variant - - - - - - rs2043515 15:88431434 T 4916 NM_001012338.2 Transcript intron_variant - - - - - - rs2043515 15:88431434 T CCDS10340.1 CCDS10340.1 Transcript intron_variant - - - - - - rs2043515 15:88431434 T ENSESTG00000005315 ENSESTT00000013519 Transcript intron_variant - - - - - - rs2043515 15:88431434 T CCDS58399.1 CCDS58399.1 Transcript intron_variant - - - - - - rs2043515 15:88431434 T 4916 NM_001243101.1 Transcript intron_variant - - - - - - rs2043515 15:88431434 T CCDS32322.1 CCDS32322.1 Transcript intron_variant - - - - - - rs2043515 15:88431434 T 4916 NM_002530.3 Transcript intron_variant - - - - - - rs920068 15:88479928 C 4916 NM_001012338.2 Transcript intron_variant - - - - - - rs920068 15:88479928 C CCDS10340.1 CCDS10340.1 Transcript intron_variant - - - - - - rs920068 15:88479928 C CCDS58399.1 CCDS58399.1 Transcript intron_variant - - - - - - rs920068 15:88479928 C 4916 NM_001243101.1 Transcript intron_variant - - - - - - rs920068 15:88479928 C ENSESTG00000005315 ENSESTT00000013515 Transcript upstream_gene_variant - - - - - - DISTANCE=3607 rs920068 15:88479928 C ENSESTG00000005294 ENSESTT00000013485 Transcript downstream_gene_variant - - - - - - DISTANCE=3988 rs920068 15:88479928 C ENSESTG00000005294 ENSESTT00000013474 Transcript downstream_gene_variant - - - - - - DISTANCE=3973 rs920068 15:88479928 C 4916 NM_002530.3 Transcript intron_variant - - - - - - rs920068 15:88479928 C CCDS32322.1 CCDS32322.1 Transcript intron_variant - - - - - - rs7161927 15:88914734 A - - - intergenic_variant - - - - - - rs393214 15:89641399 C ENSESTG00000014805 ENSESTT00000037180 Transcript intron_variant - - - - - - rs393214 15:89641399 C ENSESTG00000014805 ENSESTT00000037157 Transcript intron_variant - - - - - - rs393214 15:89641399 C ENSESTG00000014805 ENSESTT00000037170 Transcript intron_variant - - - - - - rs393214 15:89641399 C ENSESTG00000014805 ENSESTT00000037176 Transcript intron_variant - - - - - - rs393214 15:89641399 C ENSESTG00000014805 ENSESTT00000037151 Transcript intron_variant - - - - - - rs393214 15:89641399 C ENSESTG00000014805 ENSESTT00000037189 Transcript intron_variant - - - - - - rs393214 15:89641399 C 11057 NM_152924.4 Transcript intron_variant - - - - - - rs393214 15:89641399 C 11057 NM_007011.7 Transcript intron_variant - - - - - - rs893722 15:89970053 C - ENSR00001455024 RegulatoryFeature regulatory_region_variant - - - - - - rs893722 15:89970053 C - - - intergenic_variant - - - - - - rs1256822 15:90498459 G - - - intergenic_variant - - - - - - rs1256824 15:90501129 G - - - intergenic_variant - - - - - - rs6496704 15:91145086 G CCDS45348.1 CCDS45348.1 Transcript intron_variant - - - - - - rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059341 Transcript intron_variant - - - - - - rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059384 Transcript intron_variant - - - - - - rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059335 Transcript downstream_gene_variant - - - - - - DISTANCE=1208 rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059315 Transcript intron_variant - - - - - - rs6496704 15:91145086 G 64784 NM_001042574.2 Transcript intron_variant - - - - - - rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059366 Transcript intron_variant - - - - - - rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059342 Transcript intron_variant - - - - - - rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059349 Transcript downstream_gene_variant - - - - - - DISTANCE=2943 rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059302 Transcript intron_variant - - - - - - rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059327 Transcript downstream_gene_variant - - - - - - DISTANCE=3328 rs6496704 15:91145086 G 64784 NM_022769.4 Transcript intron_variant - - - - - - rs6496704 15:91145086 G ENSESTG00000023470 ENSESTT00000059293 Transcript intron_variant - - - - - - rs6496704 15:91145086 G CCDS32331.1 CCDS32331.1 Transcript intron_variant - - - - - - rs4641717 15:91222710 T ENSESTG00000025904 ENSESTT00000065296 Transcript downstream_gene_variant - - - - - - DISTANCE=706 rs2520088 15:91260219 G - ENSR00000239158 RegulatoryFeature regulatory_region_variant - - - - - - rs2520088 15:91260219 G 641 NM_000057.2 Transcript upstream_gene_variant - - - - - - DISTANCE=360 rs2520088 15:91260219 G ENSESTG00000023582 ENSESTT00000059477 Transcript upstream_gene_variant - - - - - - DISTANCE=346 rs12593635 15:91370373 T - - - intergenic_variant - - - - - - rs6416560 15:91672362 T ENSESTG00000014259 ENSESTT00000035740 Transcript intron_variant - - - - - - rs6416560 15:91672362 T ENSESTG00000014259 ENSESTT00000035745 Transcript intron_variant - - - - - - rs6416560 15:91672362 T ENSESTG00000014259 ENSESTT00000035752 Transcript intron_variant - - - - - - rs6416560 15:91672362 T ENSESTG00000014259 ENSESTT00000035732 Transcript intron_variant - - - - - - rs6416560 15:91672362 T 9899 NM_014848.4 Transcript intron_variant - - - - - - rs6416560 15:91672362 T ENSESTG00000014259 ENSESTT00000035728 Transcript intron_variant - - - - - - rs6416560 15:91672362 T ENSESTG00000014259 ENSESTT00000035735 Transcript intron_variant - - - - - - rs6416560 15:91672362 T 9899 NM_001167580.1 Transcript intron_variant - - - - - - rs6416560 15:91672362 T ENSESTG00000014259 ENSESTT00000035748 Transcript intron_variant - - - - - - rs8032476 15:91843233 A 9899 NM_001167580.1 Transcript 3_prime_UTR_variant 9464 - - - - - rs8032476 15:91843233 A ENSESTG00000014336 ENSESTT00000035865 Transcript upstream_gene_variant - - - - - - DISTANCE=4723 rs8032476 15:91843233 A 9899 NM_014848.4 Transcript 3_prime_UTR_variant 10037 - - - - - rs4984339 15:92650990 T CCDS45354.1 CCDS45354.1 Transcript intron_variant - - - - - - rs4984339 15:92650990 T ENSESTG00000014303 ENSESTT00000035838 Transcript downstream_gene_variant - - - - - - DISTANCE=3223 rs4984339 15:92650990 T 28232 NM_013272.3 Transcript intron_variant - - - - - - rs4984339 15:92650990 T ENSESTG00000014303 ENSESTT00000035848 Transcript intron_variant - - - - - - rs4984339 15:92650990 T ENSESTG00000027718 ENSESTT00000069872 Transcript intron_variant - - - - - - rs4984339 15:92650990 T CCDS10371.1 CCDS10371.1 Transcript intron_variant - - - - - - rs4984339 15:92650990 T 28232 NM_001145044.1 Transcript intron_variant - - - - - - rs4984339 15:92650990 T ENSESTG00000027718 ENSESTT00000069893 Transcript intron_variant - - - - - - rs8028476 15:92755071 C - - - intergenic_variant - - - - - - rs4777960 15:92869116 G - - - intergenic_variant - - - - - - rs4383085 15:92875154 G - - - intergenic_variant - - - - - - rs4777961 15:92882273 G - - - intergenic_variant - - - - - - rs4777962 15:92883372 C - - - intergenic_variant - - - - - - rs7173465 15:93029033 G CCDS10373.1 CCDS10373.1 Transcript intron_variant - - - - - - rs7173465 15:93029033 G 145858 NM_153040.2 Transcript intron_variant - - - - - - rs4777991 15:93029315 C CCDS10373.1 CCDS10373.1 Transcript intron_variant - - - - - - rs4777991 15:93029315 C 145858 NM_153040.2 Transcript intron_variant - - - - - - rs7170599 15:93209042 T ENSESTG00000028217 ENSESTT00000070943 Transcript intron_variant - - - - - - rs4777753 15:93460142 T 1106 NM_001042572.2 Transcript intron_variant - - - - - - rs4777753 15:93460142 T ENSESTG00000027841 ENSESTT00000070425 Transcript intron_variant - - - - - - rs4777753 15:93460142 T ENSESTG00000027841 ENSESTT00000070335 Transcript intron_variant - - - - - - rs4777753 15:93460142 T CCDS10374.2 CCDS10374.2 Transcript intron_variant - - - - - - rs4777753 15:93460142 T CCDS45356.1 CCDS45356.1 Transcript intron_variant - - - - - - rs4777753 15:93460142 T ENSESTG00000027841 ENSESTT00000070365 Transcript intron_variant - - - - - - rs4777753 15:93460142 T ENSESTG00000027841 ENSESTT00000070420 Transcript intron_variant - - - - - - rs4777753 15:93460142 T 1106 NM_001271.3 Transcript intron_variant - - - - - - rs964033 15:93563937 A ENSESTG00000028146 ENSESTT00000070788 Transcript intron_variant - - - - - - rs964033 15:93563937 A ENSESTG00000028167 ENSESTT00000070820 Transcript downstream_gene_variant - - - - - - DISTANCE=3785 rs964033 15:93563937 A CCDS10374.2 CCDS10374.2 Transcript intron_variant - - - - - - rs964033 15:93563937 A 1106 NM_001271.3 Transcript intron_variant - - - - - - rs4238485 15:93588336 C CCDS53974.1 CCDS53974.1 Transcript missense_variant 1269 1269 423 D/E gaT/gaG - PolyPhen=benign;SIFT=tolerated rs4238485 15:93588336 C CCDS45357.1 CCDS45357.1 Transcript missense_variant 1245 1245 415 D/E gaT/gaG - PolyPhen=benign;SIFT=tolerated rs4238485 15:93588336 C 56963 NM_001166286.1 Transcript missense_variant 1360 1197 399 D/E gaT/gaG - PolyPhen=benign;SIFT=tolerated rs4238485 15:93588336 C 56963 NM_001166289.1 Transcript missense_variant 1378 1197 399 D/E gaT/gaG - PolyPhen=benign;SIFT=tolerated rs4238485 15:93588336 C 56963 NM_001166287.1 Transcript missense_variant 1474 1197 399 D/E gaT/gaG - PolyPhen=benign;SIFT=tolerated rs4238485 15:93588336 C 56963 NM_020211.2 Transcript missense_variant 1527 1245 415 D/E gaT/gaG - PolyPhen=benign;SIFT=tolerated rs4238485 15:93588336 C CCDS53973.1 CCDS53973.1 Transcript missense_variant 1197 1197 399 D/E gaT/gaG - PolyPhen=benign;SIFT=tolerated rs4238485 15:93588336 C 56963 NM_001166283.1 Transcript missense_variant 1500 1269 423 D/E gaT/gaG - PolyPhen=benign;SIFT=tolerated rs4238485 15:93588336 C 56963 NM_001166288.1 Transcript missense_variant 1358 1197 399 D/E gaT/gaG - PolyPhen=benign;SIFT=tolerated rs4238485 15:93588336 C ENSESTG00000025218 ENSESTT00000063630 Transcript downstream_gene_variant - - - - - - DISTANCE=75 rs12440656 15:93778885 C - - - intergenic_variant - - - - - - rs12440664 15:93778956 C - - - intergenic_variant - - - - - - rs28524871 15:93784562 C - - - intergenic_variant - - - - - - rs11852691 15:94303033 G ENSESTG00000025298 ENSESTT00000063817 Transcript downstream_gene_variant - - - - - - DISTANCE=1251 rs7497728 15:94439464 G - - - intergenic_variant - - - - - - rs1433947 15:95006964 A ENSESTG00000009157 ENSESTT00000022967 Transcript intron_variant - - - - - - rs1433947 15:95006964 A ENSESTG00000009120 ENSESTT00000022883 Transcript intron_variant - - - - - - rs1433947 15:95006964 A CCDS32338.1 CCDS32338.1 Transcript intron_variant - - - - - - rs1433947 15:95006964 A 55784 NM_018349.3 Transcript intron_variant - - - - - - rs1433947 15:95006964 A CCDS53975.1 CCDS53975.1 Transcript intron_variant - - - - - - rs1433947 15:95006964 A 55784 NM_001159643.1 Transcript intron_variant - - - - - - rs4267260 15:95077941 A - - - intergenic_variant - - - - - - rs6496056 15:95402729 C ENSESTG00000009137 ENSESTT00000022938 Transcript upstream_gene_variant - - - - - - DISTANCE=2555 rs6496056 15:95402729 C ENSESTG00000009137 ENSESTT00000022926 Transcript upstream_gene_variant - - - - - - DISTANCE=2489 rs6496056 15:95402729 C ENSESTG00000009137 ENSESTT00000022943 Transcript upstream_gene_variant - - - - - - DISTANCE=2675 rs6496056 15:95402729 C ENSESTG00000009137 ENSESTT00000022932 Transcript upstream_gene_variant - - - - - - DISTANCE=2551 rs4247086 15:95463545 A - - - intergenic_variant - - - - - - rs7163577 15:95800241 A - - - intergenic_variant - - - - - - rs4572335 15:95892866 T - - - intergenic_variant - - - - - - rs8024332 15:95933795 C - - - intergenic_variant - - - - - - rs6496104 15:95955414 G - - - intergenic_variant - - - - - - rs4544197 15:96099784 C - - - intergenic_variant - - - - - - rs7164960 15:96162856 A - - - intergenic_variant - - - - - - rs4984463 15:96453469 G - - - intergenic_variant - - - - - - rs4984429 15:96817387 A - ENSR00000414053 RegulatoryFeature regulatory_region_variant - - - - - - rs4984429 15:96817387 A ENSESTG00000028610 ENSESTT00000072276 Transcript upstream_gene_variant - - - - - - DISTANCE=4156 rs4984429 15:96817387 A ENSESTG00000028610 ENSESTT00000072202 Transcript intron_variant - - - - - - rs4984429 15:96817387 A ENSESTG00000028610 ENSESTT00000072236 Transcript intron_variant - - - - - - rs4984429 15:96817387 A ENSESTG00000028610 ENSESTT00000072088 Transcript intron_variant - - - - - - rs4984429 15:96817387 A ENSESTG00000028610 ENSESTT00000072149 Transcript intron_variant - - - - - - rs4984429 15:96817387 A ENSESTG00000028610 ENSESTT00000072115 Transcript intron_variant - - - - - - rs4984429 15:96817387 A ENSESTG00000028610 ENSESTT00000072270 Transcript intron_variant - - - - - - rs2398179 15:96860565 T - ENSR00000239363 RegulatoryFeature regulatory_region_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072253 Transcript intron_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072236 Transcript intron_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028756 ENSESTT00000072328 Transcript upstream_gene_variant - - - - - - DISTANCE=1136 rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072102 Transcript intron_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072212 Transcript intron_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072149 Transcript intron_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072202 Transcript intron_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072187 Transcript intron_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072088 Transcript intron_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072115 Transcript intron_variant - - - - - - rs2398179 15:96860565 T ENSESTG00000028610 ENSESTT00000072218 Transcript intron_variant - - - - - - rs2398259 15:96871144 A - ENSR00000414067 RegulatoryFeature regulatory_region_variant - - - - - - rs2398259 15:96871144 A ENSESTG00000028503 ENSESTT00000071675 Transcript upstream_gene_variant - - - - - - DISTANCE=3738 rs2398259 15:96871144 A ENSESTG00000028601 ENSESTT00000071914 Transcript downstream_gene_variant - - - - - - DISTANCE=2895 rs2398259 15:96871144 A ENSESTG00000028610 ENSESTT00000072212 Transcript upstream_gene_variant - - - - - - DISTANCE=799 rs2398259 15:96871144 A ENSESTG00000028610 ENSESTT00000072149 Transcript upstream_gene_variant - - - - - - DISTANCE=567 rs2398259 15:96871144 A ENSESTG00000028503 ENSESTT00000071684 Transcript upstream_gene_variant - - - - - - DISTANCE=4650 rs2398259 15:96871144 A 7026 NM_001145155.1 Transcript intron_variant - - - - - - rs2398259 15:96871144 A 7026 NM_001145156.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4650 rs2398259 15:96871144 A ENSESTG00000028594 ENSESTT00000071886 Transcript intron_variant - - - - - - rs2398259 15:96871144 A CCDS10375.1 CCDS10375.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4191 rs2398259 15:96871144 A ENSESTG00000028610 ENSESTT00000072236 Transcript upstream_gene_variant - - - - - - DISTANCE=894 rs2398259 15:96871144 A 7026 NM_021005.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2967 rs2398259 15:96871144 A ENSESTG00000028610 ENSESTT00000072102 Transcript upstream_gene_variant - - - - - - DISTANCE=558 rs2398259 15:96871144 A ENSESTG00000028601 ENSESTT00000071902 Transcript downstream_gene_variant - - - - - - DISTANCE=2806 rs2398259 15:96871144 A ENSESTG00000028610 ENSESTT00000072202 Transcript upstream_gene_variant - - - - - - DISTANCE=797 rs2398259 15:96871144 A ENSESTG00000028610 ENSESTT00000072088 Transcript upstream_gene_variant - - - - - - DISTANCE=554 rs2398259 15:96871144 A ENSESTG00000028610 ENSESTT00000072187 Transcript upstream_gene_variant - - - - - - DISTANCE=567 rs2398259 15:96871144 A ENSESTG00000028610 ENSESTT00000072115 Transcript upstream_gene_variant - - - - - - DISTANCE=567 rs2398259 15:96871144 A ENSESTG00000028610 ENSESTT00000072218 Transcript upstream_gene_variant - - - - - - DISTANCE=818 rs2398259 15:96871144 A CCDS45358.1 CCDS45358.1 Transcript intron_variant - - - - - - rs4965053 15:97274832 C - - - intergenic_variant - - - - - - rs2654537 15:97296094 C ENSESTG00000028568 ENSESTT00000071789 Transcript downstream_gene_variant - - - - - - DISTANCE=4910 rs234528 15:97573410 C - - - intergenic_variant - - - - - - rs1902476 15:97850034 T ENSESTG00000003944 ENSESTT00000009956 Transcript intron_variant - - - - - - rs897613 15:97892854 G - - - intergenic_variant - - - - - - rs1392673 15:98106648 C ENSESTG00000003941 ENSESTT00000009941 Transcript upstream_gene_variant - - - - - - DISTANCE=2718 rs1600526 15:98748889 G - - - intergenic_variant - - - - - - rs7174573 15:98804147 C - - - intergenic_variant - - - - - - rs7170076 15:98908809 C - - - intergenic_variant - - - - - - rs1319863 15:99227648 G - ENSR00001455508 RegulatoryFeature regulatory_region_variant - - - - - - rs1319863 15:99227648 G CCDS10378.1 CCDS10378.1 Transcript intron_variant - - - - - - rs1319863 15:99227648 G 3480 NM_000875.3 Transcript intron_variant - - - - - - rs1319863 15:99227648 G ENSESTG00000008130 ENSESTT00000020541 Transcript intron_variant - - - - - - rs4966016 15:99263092 A CCDS10378.1 CCDS10378.1 Transcript intron_variant - - - - - - rs4966016 15:99263092 A 3480 NM_000875.3 Transcript intron_variant - - - - - - rs4966016 15:99263092 A ENSESTG00000008130 ENSESTT00000020541 Transcript intron_variant - - - - - - rs4505296 15:99526124 G 145814 NM_001102612.2 Transcript intron_variant - - - - - - rs4505296 15:99526124 G CCDS53977.1 CCDS53977.1 Transcript intron_variant - - - - - - rs4505296 15:99526124 G 145814 NM_001167902.1 Transcript intron_variant - - - - - - rs2053119 15:100207850 A - ENSR00001455610 RegulatoryFeature regulatory_region_variant - - - - - - rs2053119 15:100207850 A 4205 NM_001130927.1 Transcript intron_variant - - - - - - rs2053119 15:100207850 A 4205 NM_005587.2 Transcript intron_variant - - - - - - rs2053119 15:100207850 A ENSESTG00000032731 ENSESTT00000082758 Transcript intron_variant - - - - - - rs2053119 15:100207850 A ENSESTG00000032731 ENSESTT00000082786 Transcript intron_variant - - - - - - rs2053119 15:100207850 A 4205 NM_001171894.1 Transcript intron_variant - - - - - - rs2053119 15:100207850 A 4205 NM_001130926.1 Transcript intron_variant - - - - - - rs2053119 15:100207850 A CCDS45363.1 CCDS45363.1 Transcript intron_variant - - - - - - rs2053119 15:100207850 A 4205 NM_001130928.1 Transcript intron_variant - - - - - - rs2053119 15:100207850 A ENSESTG00000032731 ENSESTT00000082776 Transcript intron_variant - - - - - - rs2053119 15:100207850 A ENSESTG00000032731 ENSESTT00000082784 Transcript intron_variant - - - - - - rs2053119 15:100207850 A ENSESTG00000032731 ENSESTT00000082794 Transcript intron_variant - - - - - - rs2053119 15:100207850 A CCDS53978.1 CCDS53978.1 Transcript intron_variant - - - - - - rs2053119 15:100207850 A CCDS45362.1 CCDS45362.1 Transcript intron_variant - - - - - - rs2053119 15:100207850 A ENSESTG00000032731 ENSESTT00000082802 Transcript intron_variant - - - - - - rs2053119 15:100207850 A ENSESTG00000032731 ENSESTT00000082752 Transcript intron_variant - - - - - - rs2053119 15:100207850 A ENSESTG00000032731 ENSESTT00000082737 Transcript intron_variant - - - - - - rs2053119 15:100207850 A CCDS58401.1 CCDS58401.1 Transcript intron_variant - - - - - - rs11247125 15:100283327 A - - - intergenic_variant - - - - - - rs2924771 15:100291239 T - - - intergenic_variant - - - - - - rs8027692 15:100543954 G ENSESTG00000032791 ENSESTT00000082833 Transcript intron_variant - - - - - - rs8027692 15:100543954 G CCDS10383.1 CCDS10383.1 Transcript intron_variant - - - - - - rs8027692 15:100543954 G 170691 NM_139057.2 Transcript intron_variant - - - - - - rs2727162 15:100581919 A ENSESTG00000032791 ENSESTT00000082833 Transcript intron_variant - - - - - - rs2727162 15:100581919 A CCDS10383.1 CCDS10383.1 Transcript intron_variant - - - - - - rs2727162 15:100581919 A 170691 NM_139057.2 Transcript intron_variant - - - - - - rs4246318 15:101273144 G - ENSR00000414516 RegulatoryFeature regulatory_region_variant - - - - - - rs4246318 15:101273144 G - - - intergenic_variant - - - - - - rs4965363 15:101644774 C - - - intergenic_variant - - - - - - rs6598450 15:101882013 A 5046 NM_138320.1 Transcript intron_variant - - - - - - rs6598450 15:101882013 A 5046 NM_002570.3 Transcript intron_variant - - - - - - rs6598450 15:101882013 A ENSESTG00000013533 ENSESTT00000033959 Transcript intron_variant - - - - - - rs6598450 15:101882013 A ENSESTG00000013533 ENSESTT00000033930 Transcript intron_variant - - - - - - rs6598450 15:101882013 A ENSESTG00000013533 ENSESTT00000033954 Transcript intron_variant - - - - - - rs6598450 15:101882013 A 5046 NM_138324.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4934 rs6598450 15:101882013 A 5046 NM_138323.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4934 rs6598450 15:101882013 A 5046 NM_138319.2 Transcript intron_variant - - - - - - rs6598450 15:101882013 A 5046 NM_138321.1 Transcript intron_variant - - - - - - rs6598450 15:101882013 A ENSESTG00000013533 ENSESTT00000033964 Transcript intron_variant - - - - - - rs6598450 15:101882013 A ENSESTG00000013533 ENSESTT00000033921 Transcript intron_variant - - - - - - rs7173900 15:101922059 A - ENSR00000414651 RegulatoryFeature regulatory_region_variant - - - - - - rs7173900 15:101922059 A ENSESTG00000013533 ENSESTT00000033901 Transcript downstream_gene_variant - - - - - - DISTANCE=237 rs7173900 15:101922059 A 5046 NM_138320.1 Transcript intron_variant - - - - - - rs7173900 15:101922059 A 5046 NM_002570.3 Transcript intron_variant - - - - - - rs7173900 15:101922059 A ENSESTG00000013533 ENSESTT00000033910 Transcript intron_variant - - - - - - rs7173900 15:101922059 A ENSESTG00000013533 ENSESTT00000033898 Transcript intron_variant - - - - - - rs7173900 15:101922059 A ENSESTG00000013533 ENSESTT00000033905 Transcript downstream_gene_variant - - - - - - DISTANCE=237 rs7173900 15:101922059 A 5046 NM_138324.1 Transcript intron_variant - - - - - - rs7173900 15:101922059 A 5046 NM_138323.1 Transcript intron_variant - - - - - - rs7173900 15:101922059 A 5046 NM_138325.2 Transcript intron_variant - - - - - - rs7173900 15:101922059 A 5046 NM_138322.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1894 rs7173900 15:101922059 A 5046 NM_138319.2 Transcript intron_variant - - - - - - rs7173900 15:101922059 A 5046 NM_138321.1 Transcript intron_variant - - - - - - rs7173900 15:101922059 A ENSESTG00000013533 ENSESTT00000033921 Transcript intron_variant - - - - - - rs1167336 15:102463748 A 26682 NM_001004195.2 Transcript upstream_gene_variant - - - - - - DISTANCE=486 rs1167336 15:102463748 A CCDS32343.1 CCDS32343.1 Transcript upstream_gene_variant - - - - - - DISTANCE=486 rs183360 16:103517 C - ENSR00000501920 RegulatoryFeature regulatory_region_variant - - - - - - rs183360 16:103517 C 64285 NM_022450.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4541 rs183360 16:103517 C ENSESTG00000018832 ENSESTT00000047412 Transcript upstream_gene_variant - - - - - - DISTANCE=3000 rs183360 16:103517 C CCDS10395.1 CCDS10395.1 Transcript missense_variant 70 70 24 S/A Tcc/Gcc - PolyPhen=benign;SIFT=tolerated rs183360 16:103517 C 51728 NM_016310.3 Transcript missense_variant 116 70 24 S/A Tcc/Gcc - PolyPhen=benign;SIFT=tolerated rs183360 16:103517 C 79622 NM_024571.3 Transcript upstream_gene_variant - - - - - - DISTANCE=312 rs183360 16:103517 C ENSESTG00000018816 ENSESTT00000047393 Transcript upstream_gene_variant - - - - - - DISTANCE=361 rs183360 16:103517 C CCDS10396.1 CCDS10396.1 Transcript upstream_gene_variant - - - - - - DISTANCE=473 rs183360 16:103517 C ENSESTG00000023142 ENSESTT00000058412 Transcript downstream_gene_variant - - - - - - DISTANCE=4542 rs183360 16:103517 C CCDS32344.1 CCDS32344.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4822 rs183360 16:103517 C ENSESTG00000023312 ENSESTT00000058862 Transcript missense_variant 75 70 24 S/A Tcc/Gcc - PolyPhen=benign;SIFT=tolerated rs2562159 16:125546 G 4350 NM_001015052.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2623 rs2562159 16:125546 G CCDS32345.1 CCDS32345.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2763 rs2562159 16:125546 G ENSESTG00000018843 ENSESTT00000047477 Transcript upstream_gene_variant - - - - - - DISTANCE=2715 rs2562159 16:125546 G 64285 NM_022450.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2917 rs2562159 16:125546 G ENSESTG00000023052 ENSESTT00000058269 Transcript intron_variant - - - - - - rs2562159 16:125546 G CCDS42087.1 CCDS42087.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3890 rs2562159 16:125546 G ENSESTG00000023052 ENSESTT00000058281 Transcript intron_variant - - - - - - rs2562159 16:125546 G 4350 NM_002434.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2623 rs2562159 16:125546 G ENSESTG00000023052 ENSESTT00000058291 Transcript upstream_gene_variant - - - - - - DISTANCE=1580 rs2562159 16:125546 G 4350 NM_001015054.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1472 rs2562159 16:125546 G CCDS32346.1 CCDS32346.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3746 rs2562171 16:151218 G 8131 NM_001077350.2 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057498 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057278 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057438 Transcript intron_variant - - - - - - rs2562171 16:151218 G 8131 NM_001243248.1 Transcript intron_variant - - - - - - rs2562171 16:151218 G 8131 NM_001243249.1 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057477 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057425 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057393 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057464 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057390 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057529 Transcript upstream_gene_variant - - - - - - DISTANCE=435 rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057551 Transcript upstream_gene_variant - - - - - - DISTANCE=435 rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057451 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057510 Transcript intron_variant - - - - - - rs2562171 16:151218 G 8131 NM_001243247.1 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057493 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057293 Transcript intron_variant - - - - - - rs2562171 16:151218 G 8131 NM_001039476.2 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057515 Transcript intron_variant - - - - - - rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057549 Transcript upstream_gene_variant - - - - - - DISTANCE=435 rs2562171 16:151218 G ENSESTG00000022676 ENSESTT00000057524 Transcript intron_variant - - - - - - rs8044466 16:210054 G ENSESTG00000018894 ENSESTT00000047568 Transcript upstream_gene_variant - - - - - - DISTANCE=3025 rs1143873 16:384262 C ENSESTG00000021903 ENSESTT00000055286 Transcript intron_variant - - - - - - rs1143873 16:384262 C CCDS10406.1 CCDS10406.1 Transcript intron_variant - - - - - - rs1143873 16:384262 C CCDS10405.1 CCDS10405.1 Transcript intron_variant - - - - - - rs1143873 16:384262 C 8312 NM_181050.2 Transcript intron_variant - - - - - - rs1143873 16:384262 C ENSESTG00000021903 ENSESTT00000055290 Transcript intron_variant - - - - - - rs1143873 16:384262 C ENSESTG00000021903 ENSESTT00000055221 Transcript intron_variant - - - - - - rs1143873 16:384262 C ENSESTG00000021903 ENSESTT00000055185 Transcript intron_variant - - - - - - rs1143873 16:384262 C ENSESTG00000021903 ENSESTT00000055074 Transcript intron_variant - - - - - - rs1143873 16:384262 C 8312 NM_003502.3 Transcript intron_variant - - - - - - rs12447874 16:679814 C - ENSR00000147192 RegulatoryFeature regulatory_region_variant - - - - - - rs12447874 16:679814 C ENSESTG00000019841 ENSESTT00000049729 Transcript upstream_gene_variant - - - - - - DISTANCE=1136 rs12447874 16:679814 C 57799 NM_021168.4 Transcript downstream_gene_variant - - - - - - DISTANCE=541 rs12447874 16:679814 C CCDS45367.1 CCDS45367.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4783 rs12447874 16:679814 C 117166 NM_053284.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1198 rs12447874 16:679814 C 84326 NM_001040161.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4615 rs12447874 16:679814 C CCDS42091.1 CCDS42091.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4712 rs12447874 16:679814 C ENSESTG00000021584 ENSESTT00000054167 Transcript downstream_gene_variant - - - - - - DISTANCE=4617 rs12447874 16:679814 C 57799 NM_001172664.1 Transcript downstream_gene_variant - - - - - - DISTANCE=541 rs12447874 16:679814 C CCDS10413.1 CCDS10413.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2192 rs12447874 16:679814 C 84326 NM_001040162.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4615 rs12447874 16:679814 C 84326 NM_001040165.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4615 rs12447874 16:679814 C 57799 NM_001172663.1 Transcript downstream_gene_variant - - - - - - DISTANCE=541 rs12447874 16:679814 C 57799 NM_001172666.1 Transcript downstream_gene_variant - - - - - - DISTANCE=541 rs12447874 16:679814 C CCDS10414.1 CCDS10414.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1440 rs12447874 16:679814 C CCDS45368.1 CCDS45368.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4783 rs12447874 16:679814 C ENSESTG00000019779 ENSESTT00000049686 Transcript downstream_gene_variant - - - - - - DISTANCE=3774 rs12447874 16:679814 C 84326 NM_001040160.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4615 rs12447874 16:679814 C CCDS42090.1 CCDS42090.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4712 rs12447874 16:679814 C ENSESTG00000019779 ENSESTT00000049703 Transcript downstream_gene_variant - - - - - - DISTANCE=3731 rs12447874 16:679814 C 57799 NM_001172665.1 Transcript downstream_gene_variant - - - - - - DISTANCE=541 rs12447874 16:679814 C 84326 NM_032366.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4615 rs12447874 16:679814 C CCDS32352.1 CCDS32352.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4783 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050497 Transcript downstream_gene_variant - - - - - - DISTANCE=1471 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050477 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050613 Transcript upstream_gene_variant - - - - - - DISTANCE=2656 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050474 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050437 Transcript downstream_gene_variant - - - - - - DISTANCE=1375 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050339 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050620 Transcript upstream_gene_variant - - - - - - DISTANCE=4544 rs10903018 16:712127 G 197335 NM_145294.4 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050384 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050321 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000021579 ENSESTT00000054142 Transcript downstream_gene_variant - - - - - - DISTANCE=834 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050482 Transcript downstream_gene_variant - - - - - - DISTANCE=1375 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050603 Transcript upstream_gene_variant - - - - - - DISTANCE=1399 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050590 Transcript upstream_gene_variant - - - - - - DISTANCE=1399 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050398 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050419 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050440 Transcript downstream_gene_variant - - - - - - DISTANCE=1471 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050450 Transcript downstream_gene_variant - - - - - - DISTANCE=1471 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050629 Transcript upstream_gene_variant - - - - - - DISTANCE=4777 rs10903018 16:712127 G CCDS42092.1 CCDS42092.1 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050475 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050596 Transcript upstream_gene_variant - - - - - - DISTANCE=1399 rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050428 Transcript intron_variant - - - - - - rs10903018 16:712127 G ENSESTG00000019982 ENSESTT00000050435 Transcript downstream_gene_variant - - - - - - DISTANCE=1375 rs8056569 16:783705 T - ENSR00000664478 RegulatoryFeature regulatory_region_variant - - - - - - rs8056569 16:783705 T CCDS10425.1 CCDS10425.1 Transcript intron_variant - - - - - - rs8056569 16:783705 T ENSESTG00000020619 ENSESTT00000051757 Transcript downstream_gene_variant - - - - - - DISTANCE=3990 rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053009 Transcript downstream_gene_variant - - - - - - DISTANCE=373 rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053052 Transcript downstream_gene_variant - - - - - - DISTANCE=4276 rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053106 Transcript downstream_gene_variant - - - - - - DISTANCE=373 rs8056569 16:783705 T ENSESTG00000020605 ENSESTT00000051699 Transcript 5_prime_UTR_variant 342 - - - - - rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053066 Transcript downstream_gene_variant - - - - - - DISTANCE=373 rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000052997 Transcript downstream_gene_variant - - - - - - DISTANCE=373 rs8056569 16:783705 T 84264 NM_032304.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3990 rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053116 Transcript downstream_gene_variant - - - - - - DISTANCE=373 rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053075 Transcript downstream_gene_variant - - - - - - DISTANCE=373 rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053214 Transcript intron_variant - - - - - - rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053255 Transcript upstream_gene_variant - - - - - - DISTANCE=296 rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053043 Transcript intron_variant - - - - - - rs8056569 16:783705 T ENSESTG00000021109 ENSESTT00000053085 Transcript downstream_gene_variant - - - - - - DISTANCE=373 rs8056569 16:783705 T 64428 NM_022493.1 Transcript intron_variant - - - - - - rs8056569 16:783705 T CCDS32354.1 CCDS32354.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4249 rs8056569 16:783705 T ENSESTG00000020619 ENSESTT00000051731 Transcript downstream_gene_variant - - - - - - DISTANCE=3991 rs8056569 16:783705 T ENSESTG00000020605 ENSESTT00000051686 Transcript 5_prime_UTR_variant 430 - - - - - rs66534936 16:909804 G - ENSR00000502114 RegulatoryFeature regulatory_region_variant - - - - - - rs66534936 16:909804 G ENSESTG00000020935 ENSESTT00000052753 Transcript intron_variant - - - - - - rs66534936 16:909804 G 64788 NR_033645.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs66534936 16:909804 G ENSESTG00000020935 ENSESTT00000052688 Transcript intron_variant - - - - - - rs66534936 16:909804 G CCDS45373.1 CCDS45373.1 Transcript intron_variant - - - - - - rs66534936 16:909804 G 64788 NM_022773.2 Transcript intron_variant - - - - - - rs66534936 16:909804 G 64788 NR_033646.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs582349 16:910833 G ENSESTG00000020935 ENSESTT00000052753 Transcript intron_variant - - - - - - rs582349 16:910833 G 64788 NR_033645.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs582349 16:910833 G ENSESTG00000020935 ENSESTT00000052688 Transcript intron_variant - - - - - - rs582349 16:910833 G CCDS45373.1 CCDS45373.1 Transcript intron_variant - - - - - - rs582349 16:910833 G 64788 NM_022773.2 Transcript intron_variant - - - - - - rs582349 16:910833 G 64788 NR_033646.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs452487 16:982821 C ENSESTG00000020922 ENSESTT00000052483 Transcript intron_variant - - - - - - rs452487 16:982821 C ENSESTG00000020935 ENSESTT00000052561 Transcript intron_variant - - - - - - rs452487 16:982821 C ENSESTG00000020935 ENSESTT00000052688 Transcript intron_variant - - - - - - rs452487 16:982821 C ENSESTG00000020935 ENSESTT00000052709 Transcript intron_variant - - - - - - rs452487 16:982821 C ENSESTG00000020935 ENSESTT00000052732 Transcript intron_variant - - - - - - rs452487 16:982821 C ENSESTG00000020935 ENSESTT00000052527 Transcript intron_variant - - - - - - rs452487 16:982821 C 64788 NR_033645.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs452487 16:982821 C ENSESTG00000020935 ENSESTT00000052719 Transcript downstream_gene_variant - - - - - - DISTANCE=1294 rs452487 16:982821 C ENSESTG00000020935 ENSESTT00000052537 Transcript intron_variant - - - - - - rs452487 16:982821 C CCDS45373.1 CCDS45373.1 Transcript intron_variant - - - - - - rs452487 16:982821 C 64788 NR_033646.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs452487 16:982821 C 64788 NM_022773.2 Transcript intron_variant - - - - - - rs429469 16:991508 C ENSESTG00000020935 ENSESTT00000052561 Transcript intron_variant - - - - - - rs429469 16:991508 C ENSESTG00000020935 ENSESTT00000052688 Transcript intron_variant - - - - - - rs429469 16:991508 C ENSESTG00000020935 ENSESTT00000052709 Transcript intron_variant - - - - - - rs429469 16:991508 C ENSESTG00000020935 ENSESTT00000052732 Transcript intron_variant - - - - - - rs429469 16:991508 C ENSESTG00000020935 ENSESTT00000052527 Transcript intron_variant - - - - - - rs429469 16:991508 C 64788 NR_033645.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs429469 16:991508 C ENSESTG00000020935 ENSESTT00000052719 Transcript intron_variant - - - - - - rs429469 16:991508 C ENSESTG00000020935 ENSESTT00000052537 Transcript intron_variant - - - - - - rs429469 16:991508 C CCDS45373.1 CCDS45373.1 Transcript intron_variant - - - - - - rs429469 16:991508 C 64788 NR_033646.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs429469 16:991508 C 64788 NM_022773.2 Transcript intron_variant - - - - - - rs553256 16:1026910 C - ENSR00001502973 RegulatoryFeature regulatory_region_variant - - - - - - rs553256 16:1026910 C ENSESTG00000028113 ENSESTT00000070702 Transcript upstream_gene_variant - - - - - - DISTANCE=4899 rs553256 16:1026910 C 64788 NR_036442.1 Transcript non_coding_exon_variant,nc_transcript_variant 602 - - - - - rs553256 16:1026910 C 64788 NR_033645.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs553256 16:1026910 C 30812 NM_014587.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4898 rs237674 16:1034834 C ENSESTG00000028113 ENSESTT00000070702 Transcript synonymous_variant 903 789 263 N aaT/aaC - rs237674 16:1034834 C 64788 NR_036442.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3516 rs237674 16:1034834 C 64788 NR_033645.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3516 rs237674 16:1034834 C CCDS10428.1 CCDS10428.1 Transcript synonymous_variant 789 789 263 N aaT/aaC - rs237674 16:1034834 C 30812 NM_014587.3 Transcript synonymous_variant 904 789 263 N aaT/aaC - rs2729579 16:1168642 C - - - intergenic_variant - - - - - - rs4307951 16:1205600 G 8912 NM_021098.2 Transcript intron_variant - - - - - - rs4307951 16:1205600 G ENSESTG00000028131 ENSESTT00000070832 Transcript intron_variant - - - - - - rs4307951 16:1205600 G CCDS45375.1 CCDS45375.1 Transcript intron_variant - - - - - - rs4307951 16:1205600 G 8912 NM_001005407.1 Transcript intron_variant - - - - - - rs4307951 16:1205600 G ENSESTG00000028131 ENSESTT00000070855 Transcript intron_variant - - - - - - rs4307951 16:1205600 G CCDS45376.1 CCDS45376.1 Transcript intron_variant - - - - - - rs7201975 16:1211555 C 8912 NM_021098.2 Transcript intron_variant - - - - - - rs7201975 16:1211555 C ENSESTG00000028131 ENSESTT00000070832 Transcript intron_variant - - - - - - rs7201975 16:1211555 C CCDS45375.1 CCDS45375.1 Transcript intron_variant - - - - - - rs7201975 16:1211555 C 8912 NM_001005407.1 Transcript intron_variant - - - - - - rs7201975 16:1211555 C ENSESTG00000028131 ENSESTT00000070855 Transcript intron_variant - - - - - - rs7201975 16:1211555 C CCDS45376.1 CCDS45376.1 Transcript intron_variant - - - - - - rs224236 16:3277298 G ENSESTG00000001992 ENSESTT00000004984 Transcript intron_variant - - - - - - rs224236 16:3277298 G 7752 NM_001145446.1 Transcript intron_variant - - - - - - rs224236 16:3277298 G 7752 NM_198087.2 Transcript intron_variant - - - - - - rs224236 16:3277298 G CCDS10497.1 CCDS10497.1 Transcript intron_variant - - - - - - rs224236 16:3277298 G 7752 NM_003454.3 Transcript intron_variant - - - - - - rs224236 16:3277298 G CCDS42112.1 CCDS42112.1 Transcript intron_variant - - - - - - rs224236 16:3277298 G CCDS45395.1 CCDS45395.1 Transcript intron_variant - - - - - - rs224236 16:3277298 G ENSESTG00000001644 ENSESTT00000003960 Transcript downstream_gene_variant - - - - - - DISTANCE=2519 rs224236 16:3277298 G 7752 NM_198088.2 Transcript intron_variant - - - - - - rs224236 16:3277298 G 7752 NM_001145448.1 Transcript intron_variant - - - - - - rs224236 16:3277298 G 7752 NM_001145447.1 Transcript intron_variant - - - - - - rs224228 16:3307719 G 4210 NM_000243.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1092 rs224228 16:3307719 G CCDS55981.1 CCDS55981.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1132 rs224228 16:3307719 G 4210 NM_001198536.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1092 rs224228 16:3307719 G CCDS10498.1 CCDS10498.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1132 rs224229 16:3308166 C 4210 NM_000243.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1539 rs224229 16:3308166 C CCDS55981.1 CCDS55981.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1579 rs224229 16:3308166 C 4210 NM_001198536.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1539 rs224229 16:3308166 C CCDS10498.1 CCDS10498.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1579 rs37842 16:3370741 A ENSESTG00000001669 ENSESTT00000004087 Transcript downstream_gene_variant - - - - - - DISTANCE=3497 rs37842 16:3370741 A 7627 NM_153028.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2165 rs37842 16:3370741 A ENSESTG00000001669 ENSESTT00000004080 Transcript downstream_gene_variant - - - - - - DISTANCE=3427 rs37842 16:3370741 A ENSESTG00000001669 ENSESTT00000004073 Transcript downstream_gene_variant - - - - - - DISTANCE=3427 rs37842 16:3370741 A CCDS10501.1 CCDS10501.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2872 rs1231070 16:3416762 C 100463285 NM_001190476.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4291 rs1231070 16:3416762 C ENSESTG00000001683 ENSESTT00000004160 Transcript intron_variant - - - - - - rs1231070 16:3416762 C ENSESTG00000001683 ENSESTT00000004157 Transcript intron_variant - - - - - - rs6500560 16:3972957 G - - - intergenic_variant - - - - - - rs9932121 16:4051687 C 115 NM_001116.3 Transcript intron_variant - - - - - - rs9932121 16:4051687 C CCDS32382.1 CCDS32382.1 Transcript intron_variant - - - - - - rs9932121 16:4051687 C ENSESTG00000021231 ENSESTT00000053385 Transcript intron_variant - - - - - - rs9932121 16:4051687 C ENSESTG00000021231 ENSESTT00000053391 Transcript intron_variant - - - - - - rs9932121 16:4051687 C ENSESTG00000021231 ENSESTT00000053321 Transcript intron_variant - - - - - - rs2531970 16:4052020 G 115 NM_001116.3 Transcript intron_variant - - - - - - rs2531970 16:4052020 G CCDS32382.1 CCDS32382.1 Transcript intron_variant - - - - - - rs2531970 16:4052020 G ENSESTG00000021231 ENSESTT00000053385 Transcript intron_variant - - - - - - rs2531970 16:4052020 G ENSESTG00000021231 ENSESTT00000053391 Transcript intron_variant - - - - - - rs2531970 16:4052020 G ENSESTG00000021231 ENSESTT00000053321 Transcript intron_variant - - - - - - rs2601829 16:4103741 C - ENSR00001503176 RegulatoryFeature regulatory_region_variant - - - - - - rs2601829 16:4103741 C 115 NM_001116.3 Transcript intron_variant - - - - - - rs2601829 16:4103741 C CCDS32382.1 CCDS32382.1 Transcript intron_variant - - - - - - rs2601829 16:4103741 C ENSESTG00000021231 ENSESTT00000053385 Transcript intron_variant - - - - - - rs2601829 16:4103741 C ENSESTG00000021231 ENSESTT00000053321 Transcript intron_variant - - - - - - rs2532025 16:4103743 C - ENSR00001503176 RegulatoryFeature regulatory_region_variant - - - - - - rs2532025 16:4103743 C 115 NM_001116.3 Transcript intron_variant - - - - - - rs2532025 16:4103743 C CCDS32382.1 CCDS32382.1 Transcript intron_variant - - - - - - rs2532025 16:4103743 C ENSESTG00000021231 ENSESTT00000053385 Transcript intron_variant - - - - - - rs2532025 16:4103743 C ENSESTG00000021231 ENSESTT00000053321 Transcript intron_variant - - - - - - rs767611 16:4110736 A 115 NM_001116.3 Transcript intron_variant - - - - - - rs767611 16:4110736 A CCDS32382.1 CCDS32382.1 Transcript intron_variant - - - - - - rs767611 16:4110736 A ENSESTG00000021231 ENSESTT00000053385 Transcript intron_variant - - - - - - rs767611 16:4110736 A ENSESTG00000021231 ENSESTT00000053321 Transcript intron_variant - - - - - - rs621867 16:4390647 C CCDS10512.1 CCDS10512.1 Transcript intron_variant - - - - - - rs621867 16:4390647 C CCDS10511.1 CCDS10511.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3122 rs621867 16:4390647 C ENSESTG00000019853 ENSESTT00000049816 Transcript downstream_gene_variant - - - - - - DISTANCE=3509 rs621867 16:4390647 C ENSESTG00000021098 ENSESTT00000053014 Transcript intron_variant - - - - - - rs621867 16:4390647 C 100529144 NM_001201479.1 Transcript intron_variant - - - - - - rs621867 16:4390647 C CCDS58418.1 CCDS58418.1 Transcript intron_variant - - - - - - rs621867 16:4390647 C ENSESTG00000021098 ENSESTT00000053028 Transcript intron_variant - - - - - - rs621867 16:4390647 C 51025 NM_016069.9 Transcript intron_variant - - - - - - rs621867 16:4390647 C 84662 NM_032575.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1049 rs2085329 16:4861709 C ENSESTG00000020486 ENSESTT00000051679 Transcript missense_variant 1252 1119 373 H/Q caC/caG - rs2085329 16:4861709 C ENSESTG00000020486 ENSESTT00000051643 Transcript missense_variant 1148 1134 378 H/Q caC/caG - PolyPhen=benign;SIFT=tolerated rs2085329 16:4861709 C ENSESTG00000020486 ENSESTT00000051743 Transcript intron_variant - - - - - - rs2085329 16:4861709 C ENSESTG00000020486 ENSESTT00000051608 Transcript missense_variant 1346 1326 442 H/Q caC/caG - PolyPhen=benign;SIFT=tolerated rs2085329 16:4861709 C ENSESTG00000020486 ENSESTT00000051673 Transcript missense_variant 1303 1170 390 H/Q caC/caG - rs2085329 16:4861709 C CCDS10524.1 CCDS10524.1 Transcript missense_variant 1377 1377 459 H/Q caC/caG - PolyPhen=benign;SIFT=tolerated rs2085329 16:4861709 C 84656 NM_032569.3 Transcript missense_variant 1414 1377 459 H/Q caC/caG - PolyPhen=benign;SIFT=tolerated rs2085329 16:4861709 C ENSESTG00000020486 ENSESTT00000051591 Transcript missense_variant 1397 1377 459 H/Q caC/caG - PolyPhen=benign;SIFT=tolerated rs1008072 16:5065356 C 9717 NM_014692.1 Transcript 3_prime_UTR_variant 2656 - - - - - rs1008072 16:5065356 C CCDS45403.1 CCDS45403.1 Transcript downstream_gene_variant - - - - - - DISTANCE=385 rs2937113 16:5075246 G - ENSR00000050762 RegulatoryFeature regulatory_region_variant - - - - - - rs2937113 16:5075246 G CCDS10527.1 CCDS10527.1 Transcript downstream_gene_variant - - - - - - DISTANCE=233 rs2937113 16:5075246 G ENSESTG00000011439 ENSESTT00000028713 Transcript downstream_gene_variant - - - - - - DISTANCE=2875 rs2937113 16:5075246 G ENSESTG00000011439 ENSESTT00000028744 Transcript downstream_gene_variant - - - - - - DISTANCE=232 rs2937113 16:5075246 G ENSESTG00000011251 ENSESTT00000028192 Transcript intron_variant - - - - - - rs2937113 16:5075246 G ENSESTG00000011439 ENSESTT00000028728 Transcript intron_variant - - - - - - rs2937113 16:5075246 G ENSESTG00000011439 ENSESTT00000028722 Transcript downstream_gene_variant - - - - - - DISTANCE=2738 rs2937113 16:5075246 G ENSESTG00000011439 ENSESTT00000028738 Transcript downstream_gene_variant - - - - - - DISTANCE=2919 rs2937113 16:5075246 G 51172 NM_016256.3 Transcript 3_prime_UTR_variant 1808 - - - - - rs8057204 16:5094191 C CCDS42116.2 CCDS42116.2 Transcript downstream_gene_variant - - - - - - DISTANCE=393 rs8057204 16:5094191 C 146556 NM_001098514.2 Transcript 3_prime_UTR_variant 1481 - - - - - rs8057204 16:5094191 C ENSESTG00000011407 ENSESTT00000028640 Transcript 3_prime_UTR_variant 508 - - - - - rs8057204 16:5094191 C ENSESTG00000011254 ENSESTT00000028199 Transcript downstream_gene_variant - - - - - - DISTANCE=1500 rs8057204 16:5094191 C 100507589 NR_038913.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1219 rs8057204 16:5094191 C 146556 NM_152459.4 Transcript 3_prime_UTR_variant 1839 - - - - - rs8057204 16:5094191 C CCDS45404.2 CCDS45404.2 Transcript downstream_gene_variant - - - - - - DISTANCE=158 rs8057204 16:5094191 C ENSESTG00000011407 ENSESTT00000028646 Transcript 3_prime_UTR_variant 361 - - - - - rs7203316 16:5100009 A CCDS42116.2 CCDS42116.2 Transcript intron_variant - - - - - - rs7203316 16:5100009 A CCDS45404.2 CCDS45404.2 Transcript intron_variant - - - - - - rs7203316 16:5100009 A 146556 NM_152459.4 Transcript intron_variant - - - - - - rs7203316 16:5100009 A 146556 NM_001098514.2 Transcript intron_variant - - - - - - rs7203316 16:5100009 A ENSESTG00000011407 ENSESTT00000028646 Transcript intron_variant - - - - - - rs7203316 16:5100009 A ENSESTG00000011407 ENSESTT00000028640 Transcript intron_variant - - - - - - rs6500667 16:5255804 C - ENSR00000503076 RegulatoryFeature regulatory_region_variant - - - - - - rs6500667 16:5255804 C - - - intergenic_variant - - - - - - rs4786644 16:5257260 C - ENSR00000503077 RegulatoryFeature regulatory_region_variant - - - - - - rs4786644 16:5257260 C - - - intergenic_variant - - - - - - rs1406179 16:5269959 T - - - intergenic_variant - - - - - - rs2333778 16:5286975 C - - - intergenic_variant - - - - - - rs1830305 16:5306066 G - - - intergenic_variant - - - - - - rs3965828 16:5314497 G - - - intergenic_variant - - - - - - rs7202059 16:5349001 T - - - intergenic_variant - - - - - - rs6500678 16:5367145 C - - - intergenic_variant - - - - - - rs1919062 16:5367293 G - - - intergenic_variant - - - - - - rs4786672 16:5372784 C - ENSR00001503260 RegulatoryFeature regulatory_region_variant - - - - - - rs4786672 16:5372784 C - - - intergenic_variant - - - - - - rs1830307 16:5374124 C - ENSR00000503087 RegulatoryFeature regulatory_region_variant - - - - - - rs1830307 16:5374124 C - - - intergenic_variant - - - - - - rs7191768 16:5376946 G - - - intergenic_variant - - - - - - rs8049260 16:5377217 A - - - intergenic_variant - - - - - - rs1320112 16:5382191 G - - - intergenic_variant - - - - - - rs2341520 16:5382633 A - - - intergenic_variant - - - - - - rs8046089 16:5385125 G - - - intergenic_variant - - - - - - rs1528327 16:5385998 G - - - intergenic_variant - - - - - - rs938759 16:5386894 C - - - intergenic_variant - - - - - - rs4605163 16:5389093 A - - - intergenic_variant - - - - - - rs7206895 16:5406380 C - - - intergenic_variant - - - - - - rs938753 16:5408084 G - - - intergenic_variant - - - - - - rs1358488 16:5409908 G - - - intergenic_variant - - - - - - rs116164460 16:5472441 G - - - intergenic_variant - - - - - - rs59017977 16:5781031 C - - - intergenic_variant - - - - - - rs7194703 16:5781100 C - - - intergenic_variant - - - - - - rs2880590 16:5897336 G - - - intergenic_variant - - - - - - rs2052227 16:6270236 C 54715 NM_018723.3 Transcript intron_variant - - - - - - rs2052227 16:6270236 C 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs9925195 16:6277531 C 54715 NM_018723.3 Transcript intron_variant - - - - - - rs9925195 16:6277531 C 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs12921694 16:6700854 A 54715 NM_018723.3 Transcript intron_variant - - - - - - rs12921694 16:6700854 A ENSESTG00000032540 ENSESTT00000082133 Transcript intron_variant - - - - - - rs12921694 16:6700854 A 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs4786952 16:6985022 C 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs4786952 16:6985022 C 54715 NM_018723.3 Transcript intron_variant - - - - - - rs4786952 16:6985022 C 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs1994767 16:7014720 G - ENSR00000503155 RegulatoryFeature regulatory_region_variant - - - - - - rs1994767 16:7014720 G 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs1994767 16:7014720 G 54715 NM_018723.3 Transcript intron_variant - - - - - - rs1994767 16:7014720 G 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs4786955 16:7021144 G 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs4786955 16:7021144 G 54715 NM_018723.3 Transcript intron_variant - - - - - - rs4786955 16:7021144 G 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs11644283 16:7140809 T 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs11644283 16:7140809 T 54715 NM_018723.3 Transcript intron_variant - - - - - - rs11644283 16:7140809 T CCDS55984.1 CCDS55984.1 Transcript intron_variant - - - - - - rs11644283 16:7140809 T CCDS55983.1 CCDS55983.1 Transcript intron_variant - - - - - - rs11644283 16:7140809 T 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs7202555 16:7144047 C 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs7202555 16:7144047 C 54715 NM_018723.3 Transcript intron_variant - - - - - - rs7202555 16:7144047 C CCDS55984.1 CCDS55984.1 Transcript intron_variant - - - - - - rs7202555 16:7144047 C CCDS55983.1 CCDS55983.1 Transcript intron_variant - - - - - - rs7202555 16:7144047 C 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs4786972 16:7215443 T 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs4786972 16:7215443 T 54715 NM_018723.3 Transcript intron_variant - - - - - - rs4786972 16:7215443 T CCDS55984.1 CCDS55984.1 Transcript intron_variant - - - - - - rs4786972 16:7215443 T CCDS55983.1 CCDS55983.1 Transcript intron_variant - - - - - - rs4786972 16:7215443 T 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs8043861 16:7372795 G 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs8043861 16:7372795 G 54715 NM_018723.3 Transcript intron_variant - - - - - - rs8043861 16:7372795 G CCDS55984.1 CCDS55984.1 Transcript intron_variant - - - - - - rs8043861 16:7372795 G CCDS55983.1 CCDS55983.1 Transcript intron_variant - - - - - - rs8043861 16:7372795 G 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs7403941 16:7564915 C ENSESTG00000012530 ENSESTT00000031434 Transcript intron_variant - - - - - - rs7403941 16:7564915 C CCDS10532.1 CCDS10532.1 Transcript intron_variant - - - - - - rs7403941 16:7564915 C CCDS55984.1 CCDS55984.1 Transcript intron_variant - - - - - - rs7403941 16:7564915 C ENSESTG00000012530 ENSESTT00000031432 Transcript intron_variant - - - - - - rs7403941 16:7564915 C 54715 NM_145893.2 Transcript intron_variant - - - - - - rs7403941 16:7564915 C 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs7403941 16:7564915 C 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs7403941 16:7564915 C CCDS45405.1 CCDS45405.1 Transcript intron_variant - - - - - - rs7403941 16:7564915 C 54715 NM_018723.3 Transcript intron_variant - - - - - - rs7403941 16:7564915 C CCDS55983.1 CCDS55983.1 Transcript intron_variant - - - - - - rs7403941 16:7564915 C CCDS10531.1 CCDS10531.1 Transcript intron_variant - - - - - - rs7403941 16:7564915 C 54715 NM_145891.2 Transcript intron_variant - - - - - - rs7403941 16:7564915 C ENSESTG00000012530 ENSESTT00000031437 Transcript intron_variant - - - - - - rs7403941 16:7564915 C ENSESTG00000012530 ENSESTT00000031435 Transcript intron_variant - - - - - - rs7403941 16:7564915 C 54715 NM_145892.2 Transcript intron_variant - - - - - - rs9935109 16:7717625 G 54715 NM_145893.2 Transcript intron_variant - - - - - - rs9935109 16:7717625 G 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs9935109 16:7717625 G CCDS45405.1 CCDS45405.1 Transcript intron_variant - - - - - - rs9935109 16:7717625 G 54715 NM_018723.3 Transcript intron_variant - - - - - - rs9935109 16:7717625 G ENSESTG00000012530 ENSESTT00000031448 Transcript intron_variant - - - - - - rs9935109 16:7717625 G 54715 NM_145892.2 Transcript intron_variant - - - - - - rs9935109 16:7717625 G ENSESTG00000012530 ENSESTT00000031434 Transcript intron_variant - - - - - - rs9935109 16:7717625 G CCDS55984.1 CCDS55984.1 Transcript intron_variant - - - - - - rs9935109 16:7717625 G CCDS10532.1 CCDS10532.1 Transcript intron_variant - - - - - - rs9935109 16:7717625 G ENSESTG00000012530 ENSESTT00000031432 Transcript intron_variant - - - - - - rs9935109 16:7717625 G 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs9935109 16:7717625 G CCDS55983.1 CCDS55983.1 Transcript intron_variant - - - - - - rs9935109 16:7717625 G ENSESTG00000012530 ENSESTT00000031444 Transcript intron_variant - - - - - - rs9935109 16:7717625 G 54715 NM_145891.2 Transcript intron_variant - - - - - - rs9935109 16:7717625 G CCDS10531.1 CCDS10531.1 Transcript intron_variant - - - - - - rs9935109 16:7717625 G ENSESTG00000012530 ENSESTT00000031441 Transcript intron_variant - - - - - - rs7196923 16:7759164 C 54715 NM_145893.2 Transcript intron_variant - - - - - - rs7196923 16:7759164 C 54715 NM_001142333.1 Transcript intron_variant - - - - - - rs7196923 16:7759164 C CCDS45405.1 CCDS45405.1 Transcript intron_variant - - - - - - rs7196923 16:7759164 C 54715 NM_018723.3 Transcript intron_variant - - - - - - rs7196923 16:7759164 C ENSESTG00000012530 ENSESTT00000031448 Transcript intron_variant - - - - - - rs7196923 16:7759164 C 54715 NM_145892.2 Transcript intron_variant - - - - - - rs7196923 16:7759164 C ENSESTG00000012530 ENSESTT00000031434 Transcript intron_variant - - - - - - rs7196923 16:7759164 C CCDS55984.1 CCDS55984.1 Transcript intron_variant - - - - - - rs7196923 16:7759164 C CCDS10532.1 CCDS10532.1 Transcript intron_variant - - - - - - rs7196923 16:7759164 C ENSESTG00000012555 ENSESTT00000031484 Transcript downstream_gene_variant - - - - - - DISTANCE=432 rs7196923 16:7759164 C ENSESTG00000012530 ENSESTT00000031432 Transcript intron_variant - - - - - - rs7196923 16:7759164 C 54715 NM_001142334.1 Transcript intron_variant - - - - - - rs7196923 16:7759164 C CCDS55983.1 CCDS55983.1 Transcript intron_variant - - - - - - rs7196923 16:7759164 C ENSESTG00000012530 ENSESTT00000031444 Transcript intron_variant - - - - - - rs7196923 16:7759164 C 54715 NM_145891.2 Transcript intron_variant - - - - - - rs7196923 16:7759164 C CCDS10531.1 CCDS10531.1 Transcript intron_variant - - - - - - rs7196923 16:7759164 C ENSESTG00000012530 ENSESTT00000031441 Transcript intron_variant - - - - - - rs8052300 16:8018774 C - - - intergenic_variant - - - - - - rs3105670 16:8029170 A - - - intergenic_variant - - - - - - rs39571 16:8396551 C - ENSR00001503348 RegulatoryFeature regulatory_region_variant - - - - - - rs39571 16:8396551 C - - - intergenic_variant - - - - - - rs2100300 16:8427385 G - - - intergenic_variant - - - - - - rs6501103 16:8433345 C - - - intergenic_variant - - - - - - rs9806954 16:8690113 C - - - intergenic_variant - - - - - - rs11074382 16:8697561 G - - - intergenic_variant - - - - - - rs11866088 16:8720843 C ENSESTG00000015749 ENSESTT00000039511 Transcript upstream_gene_variant - - - - - - DISTANCE=1994 rs11866088 16:8720843 C ENSESTG00000015749 ENSESTT00000039495 Transcript intron_variant - - - - - - rs11866088 16:8720843 C CCDS10533.2 CCDS10533.2 Transcript intron_variant - - - - - - rs11866088 16:8720843 C ENSESTG00000015749 ENSESTT00000039503 Transcript intron_variant - - - - - - rs11866088 16:8720843 C ENSESTG00000015749 ENSESTT00000039472 Transcript intron_variant - - - - - - rs11866088 16:8720843 C 79091 NM_024109.2 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015953 ENSESTT00000039996 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015799 ENSESTT00000039723 Transcript intron_variant - - - - - - rs1273386 16:8808801 G 18 NM_000663.4 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015799 ENSESTT00000039709 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015799 ENSESTT00000039729 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015799 ENSESTT00000039714 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015799 ENSESTT00000039640 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015799 ENSESTT00000039690 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015922 ENSESTT00000039916 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015799 ENSESTT00000039696 Transcript intron_variant - - - - - - rs1273386 16:8808801 G 18 NM_020686.5 Transcript intron_variant - - - - - - rs1273386 16:8808801 G ENSESTG00000015799 ENSESTT00000039675 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015953 ENSESTT00000039996 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039745 Transcript intron_variant - - - - - - rs1273407 16:8862592 C CCDS10534.1 CCDS10534.1 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039723 Transcript intron_variant - - - - - - rs1273407 16:8862592 C 18 NM_000663.4 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039640 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039690 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015922 ENSESTT00000039916 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039696 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039759 Transcript intron_variant - - - - - - rs1273407 16:8862592 C 18 NM_020686.5 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039675 Transcript intron_variant - - - - - - rs1273407 16:8862592 C 18 NM_001127448.1 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039709 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039714 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039729 Transcript intron_variant - - - - - - rs1273407 16:8862592 C ENSESTG00000015799 ENSESTT00000039762 Transcript intron_variant - - - - - - rs11862072 16:8936600 G 5373 NM_000303.2 Transcript intron_variant - - - - - - rs11862072 16:8936600 G ENSESTG00000002062 ENSESTT00000005099 Transcript upstream_gene_variant - - - - - - DISTANCE=3105 rs11862072 16:8936600 G CCDS10536.1 CCDS10536.1 Transcript intron_variant - - - - - - rs7202680 16:9061339 G - ENSR00000270552 RegulatoryFeature regulatory_region_variant - - - - - - rs7202680 16:9061339 G CCDS32385.1 CCDS32385.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4197 rs7202680 16:9061339 G ENSESTG00000002135 ENSESTT00000005462 Transcript upstream_gene_variant - - - - - - DISTANCE=4870 rs7202680 16:9061339 G ENSESTG00000002135 ENSESTT00000005464 Transcript upstream_gene_variant - - - - - - DISTANCE=4870 rs7202680 16:9061339 G ENSESTG00000002135 ENSESTT00000005436 Transcript upstream_gene_variant - - - - - - DISTANCE=4870 rs7202680 16:9061339 G ENSESTG00000002079 ENSESTT00000005125 Transcript downstream_gene_variant - - - - - - DISTANCE=132 rs7202680 16:9061339 G ENSESTG00000002135 ENSESTT00000005459 Transcript upstream_gene_variant - - - - - - DISTANCE=4870 rs7202680 16:9061339 G 7874 NM_003470.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3998 rs7202680 16:9061339 G ENSESTG00000002135 ENSESTT00000005456 Transcript upstream_gene_variant - - - - - - DISTANCE=4870 rs43145 16:9438756 T - - - intergenic_variant - - - - - - rs7186019 16:9609713 T ENSESTG00000002093 ENSESTT00000005153 Transcript intron_variant - - - - - - rs8062614 16:9968877 C ENSESTG00000019886 ENSESTT00000049842 Transcript intron_variant - - - - - - rs8062614 16:9968877 C 2903 NM_000833.3 Transcript intron_variant - - - - - - rs8062614 16:9968877 C 2903 NM_001134407.1 Transcript intron_variant - - - - - - rs8062614 16:9968877 C 2903 NM_001134408.1 Transcript intron_variant - - - - - - rs8062614 16:9968877 C CCDS45407.1 CCDS45407.1 Transcript intron_variant - - - - - - rs8062614 16:9968877 C CCDS10539.1 CCDS10539.1 Transcript intron_variant - - - - - - rs8043877 16:10127573 C 2903 NM_000833.3 Transcript intron_variant - - - - - - rs8043877 16:10127573 C 2903 NM_001134407.1 Transcript intron_variant - - - - - - rs8043877 16:10127573 C 2903 NM_001134408.1 Transcript intron_variant - - - - - - rs8043877 16:10127573 C CCDS45407.1 CCDS45407.1 Transcript intron_variant - - - - - - rs8043877 16:10127573 C CCDS10539.1 CCDS10539.1 Transcript intron_variant - - - - - - rs1070903 16:10288579 G - - - intergenic_variant - - - - - - rs1097862 16:10326888 A - - - intergenic_variant - - - - - - rs1097890 16:10332351 A - - - intergenic_variant - - - - - - rs4780916 16:10556105 T ENSESTG00000019518 ENSESTT00000049187 Transcript intron_variant - - - - - - rs4780916 16:10556105 T 80063 NM_024997.3 Transcript intron_variant - - - - - - rs4780916 16:10556105 T 80063 NR_045815.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4780916 16:10556105 T 80063 NR_045816.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4780916 16:10556105 T ENSESTG00000019518 ENSESTT00000049168 Transcript intron_variant - - - - - - rs4780916 16:10556105 T CCDS58422.1 CCDS58422.1 Transcript intron_variant - - - - - - rs4780916 16:10556105 T ENSESTG00000019518 ENSESTT00000049041 Transcript intron_variant - - - - - - rs4780916 16:10556105 T CCDS10540.1 CCDS10540.1 Transcript intron_variant - - - - - - rs4780916 16:10556105 T 80063 NM_001256160.1 Transcript intron_variant - - - - - - rs1641789 16:10859478 T 4682 NM_002484.2 Transcript intron_variant - - - - - - rs1641789 16:10859478 T CCDS10543.1 CCDS10543.1 Transcript intron_variant - - - - - - rs1641789 16:10859478 T ENSESTG00000019638 ENSESTT00000049438 Transcript downstream_gene_variant - - - - - - DISTANCE=3509 rs1641789 16:10859478 T ENSESTG00000019638 ENSESTT00000049451 Transcript downstream_gene_variant - - - - - - DISTANCE=3509 rs1641789 16:10859478 T ENSESTG00000019638 ENSESTT00000049501 Transcript intron_variant - - - - - - rs1641789 16:10859478 T 780776 NM_001079512.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1055 rs1641789 16:10859478 T CCDS45408.1 CCDS45408.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4651 rs1641789 16:10859478 T ENSESTG00000019638 ENSESTT00000049519 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037039 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036995 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036832 Transcript intron_variant - - - - - - rs11649148 16:11125643 T CCDS45409.1 CCDS45409.1 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036911 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036979 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036813 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036929 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036954 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036891 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036959 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036854 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037027 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037014 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036903 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036880 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036986 Transcript intron_variant - - - - - - rs11649148 16:11125643 T CCDS58423.1 CCDS58423.1 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037048 Transcript intron_variant - - - - - - rs11649148 16:11125643 T 23274 NM_015226.2 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037042 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037036 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037018 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036978 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036926 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036983 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037052 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036907 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036841 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036906 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036970 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036918 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036922 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036804 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037033 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036866 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036885 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036990 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036848 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037062 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036824 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037003 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036947 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037058 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037070 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036938 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036966 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036836 Transcript intron_variant - - - - - - rs11649148 16:11125643 T 23274 NM_001243403.1 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037023 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036871 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036931 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036900 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037053 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036896 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036974 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000037046 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036913 Transcript intron_variant - - - - - - rs11649148 16:11125643 T ENSESTG00000014685 ENSESTT00000036864 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036995 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036832 Transcript intron_variant - - - - - - rs2160169 16:11222027 C CCDS45409.1 CCDS45409.1 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036911 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036979 Transcript downstream_gene_variant - - - - - - DISTANCE=1828 rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036813 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036929 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036954 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036891 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036959 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036854 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037083 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037027 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037014 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036880 Transcript intron_variant - - - - - - rs2160169 16:11222027 C CCDS58423.1 CCDS58423.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1890 rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037048 Transcript intron_variant - - - - - - rs2160169 16:11222027 C 23274 NM_015226.2 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037042 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037036 Transcript downstream_gene_variant - - - - - - DISTANCE=1828 rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037018 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036978 Transcript downstream_gene_variant - - - - - - DISTANCE=1828 rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036926 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037052 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036841 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036970 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036918 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036922 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036804 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037033 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036866 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036885 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036848 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037062 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036824 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037003 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036947 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037058 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037070 Transcript downstream_gene_variant - - - - - - DISTANCE=1828 rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036938 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036836 Transcript intron_variant - - - - - - rs2160169 16:11222027 C 23274 NM_001243403.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1826 rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036966 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037023 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036871 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036931 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036900 Transcript downstream_gene_variant - - - - - - DISTANCE=1828 rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037053 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036896 Transcript downstream_gene_variant - - - - - - DISTANCE=1828 rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036974 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000037046 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036913 Transcript intron_variant - - - - - - rs2160169 16:11222027 C ENSESTG00000014685 ENSESTT00000036864 Transcript intron_variant - - - - - - rs2550481 16:11292619 G - - - intergenic_variant - - - - - - rs12930458 16:11626134 G - ENSR00001503571 RegulatoryFeature regulatory_region_variant - - - - - - rs12930458 16:11626134 G - - - intergenic_variant - - - - - - rs2868422 16:11663679 A ENSESTG00000015072 ENSESTT00000037830 Transcript intron_variant - - - - - - rs2868422 16:11663679 A ENSESTG00000015072 ENSESTT00000037828 Transcript intron_variant - - - - - - rs2868422 16:11663679 A ENSESTG00000015072 ENSESTT00000037817 Transcript intron_variant - - - - - - rs2868422 16:11663679 A ENSESTG00000015072 ENSESTT00000037796 Transcript intron_variant - - - - - - rs2868422 16:11663679 A 9516 NM_001136472.1 Transcript intron_variant - - - - - - rs2868422 16:11663679 A 9516 NR_024320.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2868422 16:11663679 A ENSESTG00000015072 ENSESTT00000037784 Transcript intron_variant - - - - - - rs2868422 16:11663679 A 9516 NM_001136473.1 Transcript intron_variant - - - - - - rs2868422 16:11663679 A ENSESTG00000015072 ENSESTT00000037812 Transcript intron_variant - - - - - - rs2868422 16:11663679 A ENSESTG00000015072 ENSESTT00000037804 Transcript intron_variant - - - - - - rs2868422 16:11663679 A 9516 NM_004862.3 Transcript intron_variant - - - - - - rs350270 16:12238022 C ENSESTG00000002784 ENSESTT00000006887 Transcript downstream_gene_variant - - - - - - DISTANCE=3859 rs350270 16:12238022 C 92017 NM_032167.3 Transcript intron_variant - - - - - - rs350270 16:12238022 C CCDS10553.2 CCDS10553.2 Transcript intron_variant - - - - - - rs350270 16:12238022 C ENSESTG00000002740 ENSESTT00000006812 Transcript intron_variant - - - - - - rs3862467 16:12552297 C 92017 NM_032167.3 Transcript intron_variant - - - - - - rs3862467 16:12552297 C ENSESTG00000002740 ENSESTT00000006813 Transcript intron_variant - - - - - - rs3862467 16:12552297 C CCDS10553.2 CCDS10553.2 Transcript intron_variant - - - - - - rs3862467 16:12552297 C ENSESTG00000002740 ENSESTT00000006812 Transcript intron_variant - - - - - - rs8054178 16:12810958 T CCDS42119.1 CCDS42119.1 Transcript intron_variant - - - - - - rs8054178 16:12810958 T ENSESTG00000002767 ENSESTT00000006871 Transcript intron_variant - - - - - - rs8054178 16:12810958 T 100616195 NR_039869.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3220 rs8054178 16:12810958 T 55313 NM_001099455.1 Transcript intron_variant - - - - - - rs8054178 16:12810958 T ENSESTG00000002767 ENSESTT00000006874 Transcript intron_variant - - - - - - rs8054178 16:12810958 T ENSESTG00000002767 ENSESTT00000006860 Transcript intron_variant - - - - - - rs8054178 16:12810958 T CCDS42120.1 CCDS42120.1 Transcript intron_variant - - - - - - rs8054178 16:12810958 T 55313 NM_018340.2 Transcript intron_variant - - - - - - rs8054178 16:12810958 T ENSESTG00000002767 ENSESTT00000006857 Transcript intron_variant - - - - - - rs4399523 16:12871496 T CCDS42119.1 CCDS42119.1 Transcript intron_variant - - - - - - rs4399523 16:12871496 T ENSESTG00000002767 ENSESTT00000006871 Transcript intron_variant - - - - - - rs4399523 16:12871496 T 55313 NM_001099455.1 Transcript intron_variant - - - - - - rs4399523 16:12871496 T ENSESTG00000002767 ENSESTT00000006874 Transcript intron_variant - - - - - - rs4399523 16:12871496 T CCDS42120.1 CCDS42120.1 Transcript intron_variant - - - - - - rs4399523 16:12871496 T ENSESTG00000002767 ENSESTT00000006848 Transcript downstream_gene_variant - - - - - - DISTANCE=3335 rs4399523 16:12871496 T ENSESTG00000002767 ENSESTT00000006860 Transcript intron_variant - - - - - - rs4399523 16:12871496 T 55313 NM_018340.2 Transcript intron_variant - - - - - - rs4399523 16:12871496 T ENSESTG00000002767 ENSESTT00000006857 Transcript intron_variant - - - - - - rs4781370 16:13072981 C CCDS45417.2 CCDS45417.2 Transcript intron_variant - - - - - - rs4781370 16:13072981 C 729993 NM_001145204.2 Transcript intron_variant - - - - - - rs963765 16:13127602 A CCDS45417.2 CCDS45417.2 Transcript intron_variant - - - - - - rs963765 16:13127602 A 729993 NM_001145204.2 Transcript intron_variant - - - - - - rs6548208 2:21888 C ENSESTG00000025868 ENSESTT00000065191 Transcript intron_variant - - - - - - rs4619638 2:31926 C ENSESTG00000025868 ENSESTT00000065191 Transcript intron_variant - - - - - - rs12612225 2:394685 C ENSESTG00000025950 ENSESTT00000065405 Transcript intron_variant - - - - - - rs6720676 2:947006 C CCDS46220.1 CCDS46220.1 Transcript intron_variant - - - - - - rs6720676 2:947006 C 54221 NM_018968.3 Transcript intron_variant - - - - - - rs11691156 2:961688 C CCDS46220.1 CCDS46220.1 Transcript intron_variant - - - - - - rs11691156 2:961688 C 54221 NM_018968.3 Transcript intron_variant - - - - - - rs10173246 2:1007868 A CCDS46220.1 CCDS46220.1 Transcript intron_variant - - - - - - rs10173246 2:1007868 A 54221 NM_018968.3 Transcript intron_variant - - - - - - rs7566133 2:1717059 G 7837 NM_012293.1 Transcript intron_variant - - - - - - rs7566133 2:1717059 G ENSESTG00000021308 ENSESTT00000053760 Transcript intron_variant - - - - - - rs7566133 2:1717059 G CCDS46221.1 CCDS46221.1 Transcript intron_variant - - - - - - rs7566133 2:1717059 G ENSESTG00000021308 ENSESTT00000053685 Transcript intron_variant - - - - - - rs4853826 2:1872895 T ENSESTG00000021199 ENSESTT00000053388 Transcript intron_variant - - - - - - rs4853826 2:1872895 T CCDS46222.1 CCDS46222.1 Transcript intron_variant - - - - - - rs4853826 2:1872895 T ENSESTG00000021199 ENSESTT00000053394 Transcript intron_variant - - - - - - rs4853826 2:1872895 T 23040 NM_015025.2 Transcript intron_variant - - - - - - rs958609 2:2037222 C ENSESTG00000004551 ENSESTT00000011521 Transcript intron_variant - - - - - - rs958609 2:2037222 C 23040 NM_015025.2 Transcript intron_variant - - - - - - rs958609 2:2037222 C ENSESTG00000021157 ENSESTT00000053209 Transcript intron_variant - - - - - - rs6706456 2:2261279 T ENSESTG00000004551 ENSESTT00000011509 Transcript intron_variant - - - - - - rs6706456 2:2261279 T ENSESTG00000004551 ENSESTT00000011520 Transcript intron_variant - - - - - - rs6706456 2:2261279 T 23040 NM_015025.2 Transcript intron_variant - - - - - - rs2385138 2:2337226 C ENSESTG00000004551 ENSESTT00000011509 Transcript upstream_gene_variant - - - - - - DISTANCE=2079 rs2385138 2:2337226 C ENSESTG00000004551 ENSESTT00000011512 Transcript upstream_gene_variant - - - - - - DISTANCE=2194 rs2385138 2:2337226 C 23040 NM_015025.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2181 rs7591458 2:3136957 A - - - intergenic_variant - - - - - - rs896923 2:3138006 G - - - intergenic_variant - - - - - - rs11884568 2:3143908 A - - - intergenic_variant - - - - - - rs2368694 2:3147882 A - - - intergenic_variant - - - - - - rs4854103 2:3173377 C - - - intergenic_variant - - - - - - rs1979200 2:3173721 A - - - intergenic_variant - - - - - - rs7590363 2:3204308 G CCDS1651.1 CCDS1651.1 Transcript intron_variant - - - - - - rs7590363 2:3204308 G ENSESTG00000011292 ENSESTT00000028385 Transcript intron_variant - - - - - - rs7590363 2:3204308 G ENSESTG00000011292 ENSESTT00000028382 Transcript intron_variant - - - - - - rs7590363 2:3204308 G ENSESTG00000011292 ENSESTT00000028353 Transcript intron_variant - - - - - - rs7590363 2:3204308 G ENSESTG00000011292 ENSESTT00000028374 Transcript intron_variant - - - - - - rs7590363 2:3204308 G ENSESTG00000011292 ENSESTT00000028360 Transcript intron_variant - - - - - - rs7590363 2:3204308 G 7260 NM_003310.2 Transcript intron_variant - - - - - - rs7590363 2:3204308 G ENSESTG00000011292 ENSESTT00000028388 Transcript intron_variant - - - - - - rs6756734 2:3267251 C ENSESTG00000011292 ENSESTT00000028374 Transcript intron_variant - - - - - - rs6756734 2:3267251 C ENSESTG00000011292 ENSESTT00000028360 Transcript intron_variant - - - - - - rs6756734 2:3267251 C CCDS1651.1 CCDS1651.1 Transcript intron_variant - - - - - - rs6756734 2:3267251 C 7260 NM_003310.2 Transcript intron_variant - - - - - - rs6756734 2:3267251 C ENSESTG00000011292 ENSESTT00000028385 Transcript intron_variant - - - - - - rs6756734 2:3267251 C ENSESTG00000011292 ENSESTT00000028382 Transcript intron_variant - - - - - - rs6756734 2:3267251 C ENSESTG00000011292 ENSESTT00000028353 Transcript intron_variant - - - - - - rs2043081 2:3726608 C 55821 NM_018436.3 Transcript intron_variant - - - - - - rs2043081 2:3726608 C CCDS46223.1 CCDS46223.1 Transcript intron_variant - - - - - - rs2043081 2:3726608 C ENSESTG00000011250 ENSESTT00000028215 Transcript intron_variant - - - - - - rs2043081 2:3726608 C ENSESTG00000011250 ENSESTT00000028210 Transcript intron_variant - - - - - - rs11123619 2:3913662 T - - - intergenic_variant - - - - - - rs985860 2:3921535 G - - - intergenic_variant - - - - - - rs934759 2:4179951 C ENSESTG00000014529 ENSESTT00000036378 Transcript downstream_gene_variant - - - - - - DISTANCE=4275 rs2577201 2:4244597 C - - - intergenic_variant - - - - - - rs2580866 2:4935079 A - - - intergenic_variant - - - - - - rs6431968 2:5211690 G - - - intergenic_variant - - - - - - rs10153947 2:5316719 G - - - intergenic_variant - - - - - - rs11695261 2:5380459 C - - - intergenic_variant - - - - - - rs792109 2:5533493 G - - - intergenic_variant - - - - - - rs2043683 2:5692717 T ENSESTG00000024349 ENSESTT00000061552 Transcript intron_variant - - - - - - rs6727585 2:6663774 G - - - intergenic_variant - - - - - - rs978783 2:6665084 C - ENSR00001539083 RegulatoryFeature regulatory_region_variant - - - - - - rs978783 2:6665084 C - - - intergenic_variant - - - - - - rs307980 2:6847446 G - - - intergenic_variant - - - - - - rs12473204 2:6926363 C - - - intergenic_variant - - - - - - rs309325 2:7154632 C - ENSR00000675525 RegulatoryFeature regulatory_region_variant - - - - - - rs309325 2:7154632 C ENSESTG00000011689 ENSESTT00000029316 Transcript 5_prime_UTR_variant 285 - - - - - rs309325 2:7154632 C ENSESTG00000011689 ENSESTT00000029305 Transcript synonymous_variant 562 183 61 T acT/acC - rs309325 2:7154632 C ENSESTG00000011689 ENSESTT00000029322 Transcript synonymous_variant 582 183 61 T acT/acC - rs309325 2:7154632 C CCDS1657.1 CCDS1657.1 Transcript synonymous_variant 183 183 61 T acT/acC - rs309325 2:7154632 C 9781 NM_014746.3 Transcript synonymous_variant 625 183 61 T acT/acC - rs309325 2:7154632 C ENSESTG00000011689 ENSESTT00000029327 Transcript intron_variant - - - - - - rs309325 2:7154632 C ENSESTG00000011689 ENSESTT00000029308 Transcript synonymous_variant 562 183 61 T acT/acC - rs309325 2:7154632 C ENSESTG00000011689 ENSESTT00000029319 Transcript synonymous_variant 582 183 61 T acT/acC - rs309282 2:7196233 G - - - intergenic_variant - - - - - - rs270831 2:7760700 A - - - intergenic_variant - - - - - - rs181138 2:8300606 C - ENSR00001044311 RegulatoryFeature regulatory_region_variant - - - - - - rs181138 2:8300606 C 339789 NR_034135.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4669258 2:8523638 C - - - intergenic_variant - - - - - - rs905681 2:8603496 G - - - intergenic_variant - - - - - - rs4669345 2:8979995 C ENSESTG00000006238 ENSESTT00000015760 Transcript upstream_gene_variant - - - - - - DISTANCE=2269 rs4669345 2:8979995 C ENSESTG00000006238 ENSESTT00000015756 Transcript upstream_gene_variant - - - - - - DISTANCE=2252 rs4669345 2:8979995 C 57498 NM_020738.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2240 rs2666204 2:9245531 G ENSESTG00000021997 ENSESTT00000055375 Transcript downstream_gene_variant - - - - - - DISTANCE=288 rs2666204 2:9245531 G ENSESTG00000021997 ENSESTT00000055364 Transcript downstream_gene_variant - - - - - - DISTANCE=821 rs4669438 2:9862026 C - - - intergenic_variant - - - - - - rs908291 2:9910482 G - ENSR00000584968 RegulatoryFeature regulatory_region_variant - - - - - - rs908291 2:9910482 G - - - intergenic_variant - - - - - - rs11898342 2:10155122 G - ENSR00000585024 RegulatoryFeature regulatory_region_variant - - - - - - rs11898342 2:10155122 G - - - intergenic_variant - - - - - - rs2058624 2:10473811 C 3241 NM_002149.3 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071669 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071532 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071587 Transcript intron_variant - - - - - - rs2058624 2:10473811 C 3241 NM_134421.2 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071649 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071694 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071617 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071685 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071679 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071691 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071614 Transcript intron_variant - - - - - - rs2058624 2:10473811 C 3241 NM_001258357.1 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071599 Transcript intron_variant - - - - - - rs2058624 2:10473811 C ENSESTG00000028461 ENSESTT00000071651 Transcript intron_variant - - - - - - rs2110663 2:10516232 G 3241 NM_002149.3 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071711 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071705 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071669 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071532 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071649 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071702 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071617 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071691 Transcript intron_variant - - - - - - rs2110663 2:10516232 G 3241 NM_001258357.1 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071599 Transcript intron_variant - - - - - - rs2110663 2:10516232 G 3241 NM_001258358.1 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071587 Transcript intron_variant - - - - - - rs2110663 2:10516232 G 3241 NM_134421.2 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071694 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071679 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071685 Transcript intron_variant - - - - - - rs2110663 2:10516232 G 3241 NM_001258359.1 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071614 Transcript intron_variant - - - - - - rs2110663 2:10516232 G ENSESTG00000028461 ENSESTT00000071651 Transcript intron_variant - - - - - - rs4668686 2:10554720 C - ENSR00001539409 RegulatoryFeature regulatory_region_variant - - - - - - rs4668686 2:10554720 C 3241 NM_002149.3 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071711 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071705 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071669 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071532 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071649 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071702 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071617 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071691 Transcript intron_variant - - - - - - rs4668686 2:10554720 C 3241 NM_001258357.1 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071599 Transcript intron_variant - - - - - - rs4668686 2:10554720 C 3241 NM_001258358.1 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071587 Transcript intron_variant - - - - - - rs4668686 2:10554720 C 3241 NM_134421.2 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071694 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071679 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071685 Transcript intron_variant - - - - - - rs4668686 2:10554720 C 3241 NM_001258359.1 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071614 Transcript intron_variant - - - - - - rs4668686 2:10554720 C ENSESTG00000028461 ENSESTT00000071651 Transcript intron_variant - - - - - - rs818175 2:10625229 T - - - intergenic_variant - - - - - - rs1198907 2:11058214 G 3754 NM_002236.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3863 rs1198907 2:11058214 G CCDS1676.1 CCDS1676.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4177 rs4669729 2:11603838 G ENSESTG00000014825 ENSESTT00000037171 Transcript intron_variant - - - - - - rs4669729 2:11603838 G ENSESTG00000014825 ENSESTT00000037179 Transcript intron_variant - - - - - - rs4669729 2:11603838 G 1876 NM_198256.2 Transcript intron_variant - - - - - - rs4669729 2:11603838 G ENSESTG00000014825 ENSESTT00000037182 Transcript intron_variant - - - - - - rs4669729 2:11603838 G 1876 NR_003092.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4669729 2:11603838 G ENSESTG00000014825 ENSESTT00000037149 Transcript intron_variant - - - - - - rs4669729 2:11603838 G 1876 NR_003093.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4669729 2:11603838 G CCDS1680.2 CCDS1680.2 Transcript intron_variant - - - - - - rs4669729 2:11603838 G ENSESTG00000014825 ENSESTT00000037160 Transcript intron_variant - - - - - - rs4669729 2:11603838 G 1876 NR_003094.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4669729 2:11603838 G 1876 NR_003095.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6733331 2:11604618 G ENSESTG00000014825 ENSESTT00000037171 Transcript intron_variant - - - - - - rs6733331 2:11604618 G ENSESTG00000014825 ENSESTT00000037179 Transcript intron_variant - - - - - - rs6733331 2:11604618 G 1876 NM_198256.2 Transcript intron_variant - - - - - - rs6733331 2:11604618 G ENSESTG00000014825 ENSESTT00000037182 Transcript intron_variant - - - - - - rs6733331 2:11604618 G 1876 NR_003092.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6733331 2:11604618 G ENSESTG00000014825 ENSESTT00000037149 Transcript intron_variant - - - - - - rs6733331 2:11604618 G 1876 NR_003093.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6733331 2:11604618 G CCDS1680.2 CCDS1680.2 Transcript intron_variant - - - - - - rs6733331 2:11604618 G ENSESTG00000014825 ENSESTT00000037160 Transcript intron_variant - - - - - - rs6733331 2:11604618 G 1876 NR_003094.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6733331 2:11604618 G 1876 NR_003095.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10199054 2:12149422 G ENSESTG00000014787 ENSESTT00000037059 Transcript intron_variant - - - - - - rs10199054 2:12149422 G ENSESTG00000014787 ENSESTT00000037025 Transcript intron_variant - - - - - - rs10199054 2:12149422 G ENSESTG00000014787 ENSESTT00000037040 Transcript intron_variant - - - - - - rs1026313 2:12440733 C ENSESTG00000014787 ENSESTT00000037025 Transcript intron_variant - - - - - - rs490004 2:13655281 G - - - intergenic_variant - - - - - - rs10188982 2:13756745 C - - - intergenic_variant - - - - - - rs1510831 2:13792955 C - ENSR00000585568 RegulatoryFeature regulatory_region_variant - - - - - - rs1510831 2:13792955 C - - - intergenic_variant - - - - - - rs1510833 2:13793651 A - - - intergenic_variant - - - - - - rs1912550 2:13813668 T - - - intergenic_variant - - - - - - rs9808485 2:13881113 T - - - intergenic_variant - - - - - - rs1446549 2:13921533 C - - - intergenic_variant - - - - - - rs2121342 2:13922028 T - - - intergenic_variant - - - - - - rs7564383 2:14002313 T - - - intergenic_variant - - - - - - rs12995957 2:14086571 C - - - intergenic_variant - - - - - - rs2945667 2:14152452 C - - - intergenic_variant - - - - - - rs486747 2:14183055 T - - - intergenic_variant - - - - - - rs360478 2:14203493 T - - - intergenic_variant - - - - - - rs1160772 2:15051978 A - - - intergenic_variant - - - - - - rs793828 2:15098991 A - - - intergenic_variant - - - - - - rs4668456 2:15759897 A ENSESTG00000000853 ENSESTT00000002209 Transcript intron_variant - - - - - - rs4668456 2:15759897 A 1653 NM_004939.2 Transcript intron_variant - - - - - - rs4668456 2:15759897 A CCDS1686.1 CCDS1686.1 Transcript intron_variant - - - - - - rs807633 2:15773029 A ENSESTG00000000853 ENSESTT00000002209 Transcript downstream_gene_variant - - - - - - DISTANCE=2089 rs807633 2:15773029 A 1653 NM_004939.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1794 rs807633 2:15773029 A CCDS1686.1 CCDS1686.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1999 rs7562522 2:15978187 G - - - intergenic_variant - - - - - - rs11886063 2:16080157 G - ENSR00000585731 RegulatoryFeature regulatory_region_variant - - - - - - rs11886063 2:16080157 G CCDS1687.1 CCDS1687.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2030 rs11886063 2:16080157 G ENSESTG00000025231 ENSESTT00000063680 Transcript upstream_gene_variant - - - - - - DISTANCE=527 rs11886063 2:16080157 G 4613 NM_005378.4 Transcript upstream_gene_variant - - - - - - DISTANCE=526 rs11886063 2:16080157 G 10408 NR_026766.1 Transcript non_coding_exon_variant,nc_transcript_variant 633 - - - - - rs4611618 2:16185532 C - - - intergenic_variant - - - - - - rs340735 2:16424664 C - - - intergenic_variant - - - - - - rs1035307 2:17043540 T - - - intergenic_variant - - - - - - rs578089 2:17366022 T - - - intergenic_variant - - - - - - rs6531042 2:17489035 G - - - intergenic_variant - - - - - - rs10153618 2:17597001 A - - - intergenic_variant - - - - - - rs6531045 2:17600738 C - - - intergenic_variant - - - - - - rs2680831 2:17754866 T - ENSR00001539904 RegulatoryFeature regulatory_region_variant - - - - - - rs2680831 2:17754866 T ENSESTG00000008096 ENSESTT00000020501 Transcript intron_variant - - - - - - rs2680831 2:17754866 T ENSESTG00000008096 ENSESTT00000020482 Transcript intron_variant - - - - - - rs2680831 2:17754866 T ENSESTG00000008240 ENSESTT00000020799 Transcript intron_variant - - - - - - rs2680831 2:17754866 T 7447 NM_003385.4 Transcript intron_variant - - - - - - rs2710693 2:17775788 C CCDS1689.1 CCDS1689.1 Transcript intron_variant - - - - - - rs2710693 2:17775788 C ENSESTG00000008096 ENSESTT00000020501 Transcript intron_variant - - - - - - rs2710693 2:17775788 C ENSESTG00000008096 ENSESTT00000020482 Transcript intron_variant - - - - - - rs2710693 2:17775788 C ENSESTG00000008240 ENSESTT00000020799 Transcript upstream_gene_variant - - - - - - DISTANCE=2375 rs2710693 2:17775788 C 7447 NM_003385.4 Transcript intron_variant - - - - - - rs10182780 2:17893430 T ENSESTG00000008146 ENSESTT00000020785 Transcript intron_variant - - - - - - rs10182780 2:17893430 T ENSESTG00000008146 ENSESTT00000020776 Transcript intron_variant - - - - - - rs10182780 2:17893430 T ENSESTG00000008146 ENSESTT00000020663 Transcript intron_variant - - - - - - rs10182780 2:17893430 T 79677 NM_001142286.1 Transcript intron_variant - - - - - - rs10182780 2:17893430 T ENSESTG00000008146 ENSESTT00000020735 Transcript intron_variant - - - - - - rs10182780 2:17893430 T ENSESTG00000008146 ENSESTT00000020689 Transcript intron_variant - - - - - - rs10182780 2:17893430 T 79677 NM_024624.5 Transcript intron_variant - - - - - - rs10182780 2:17893430 T ENSESTG00000008146 ENSESTT00000020671 Transcript intron_variant - - - - - - rs10182780 2:17893430 T ENSESTG00000008146 ENSESTT00000020693 Transcript intron_variant - - - - - - rs10182780 2:17893430 T ENSESTG00000008146 ENSESTT00000020731 Transcript intron_variant - - - - - - rs10182780 2:17893430 T CCDS1690.1 CCDS1690.1 Transcript intron_variant - - - - - - rs2052746 2:17913266 C ENSESTG00000008146 ENSESTT00000020693 Transcript intron_variant - - - - - - rs2052746 2:17913266 C ENSESTG00000008146 ENSESTT00000020671 Transcript intron_variant - - - - - - rs2052746 2:17913266 C CCDS1690.1 CCDS1690.1 Transcript intron_variant - - - - - - rs2052746 2:17913266 C ENSESTG00000008146 ENSESTT00000020663 Transcript intron_variant - - - - - - rs2052746 2:17913266 C 79677 NM_001142286.1 Transcript intron_variant - - - - - - rs2052746 2:17913266 C ENSESTG00000008146 ENSESTT00000020689 Transcript intron_variant - - - - - - rs2052746 2:17913266 C 79677 NM_024624.5 Transcript intron_variant - - - - - - rs12328424 2:17918166 A ENSESTG00000008146 ENSESTT00000020663 Transcript intron_variant - - - - - - rs12328424 2:17918166 A 79677 NM_001142286.1 Transcript intron_variant - - - - - - rs12328424 2:17918166 A ENSESTG00000008146 ENSESTT00000020689 Transcript intron_variant - - - - - - rs12328424 2:17918166 A 79677 NM_024624.5 Transcript intron_variant - - - - - - rs12328424 2:17918166 A ENSESTG00000008146 ENSESTT00000020671 Transcript intron_variant - - - - - - rs12328424 2:17918166 A ENSESTG00000008146 ENSESTT00000020693 Transcript intron_variant - - - - - - rs12328424 2:17918166 A CCDS1690.1 CCDS1690.1 Transcript intron_variant - - - - - - rs12328424 2:17918166 A ENSESTG00000008146 ENSESTT00000020569 Transcript downstream_gene_variant - - - - - - DISTANCE=4723 rs2061608 2:18075643 A ENSESTG00000025464 ENSESTT00000064290 Transcript intron_variant - - - - - - rs2061608 2:18075643 A ENSESTG00000025464 ENSESTT00000064275 Transcript intron_variant - - - - - - rs2061608 2:18075643 A ENSESTG00000025464 ENSESTT00000064260 Transcript intron_variant - - - - - - rs2061608 2:18075643 A 3790 NM_002252.3 Transcript intron_variant - - - - - - rs6721099 2:18457089 C - - - intergenic_variant - - - - - - rs4313979 2:19041596 A - - - intergenic_variant - - - - - - rs4666388 2:19261889 T - - - intergenic_variant - - - - - - rs6724206 2:19320467 T ENSESTG00000012453 ENSESTT00000031215 Transcript intron_variant - - - - - - rs1658254 2:19478347 C ENSESTG00000012453 ENSESTT00000031215 Transcript intron_variant - - - - - - rs860366 2:19607162 G - - - intergenic_variant - - - - - - rs896808 2:19976042 T - - - intergenic_variant - - - - - - rs1377353 2:20738032 C - ENSR00000586307 RegulatoryFeature regulatory_region_variant - - - - - - rs1377353 2:20738032 C - - - intergenic_variant - - - - - - rs568413 2:21235475 C - ENSR00000675749 RegulatoryFeature regulatory_region_variant - - - - - - rs568413 2:21235475 C 338 NM_000384.2 Transcript missense_variant 4393 4265 1422 Y/C tAt/tGt - PolyPhen=benign;SIFT=tolerated rs568413 2:21235475 C ENSESTG00000012933 ENSESTT00000032439 Transcript downstream_gene_variant - - - - - - DISTANCE=3834 rs568413 2:21235475 C CCDS1703.1 CCDS1703.1 Transcript missense_variant 4265 4265 1422 Y/C tAt/tGt - PolyPhen=benign;SIFT=tolerated rs568413 2:21235475 C ENSESTG00000012933 ENSESTT00000032436 Transcript downstream_gene_variant - - - - - - DISTANCE=827 rs562956 2:21241454 T 338 NM_000384.2 Transcript intron_variant - - - - - - rs562956 2:21241454 T ENSESTG00000012933 ENSESTT00000032439 Transcript intron_variant - - - - - - rs562956 2:21241454 T CCDS1703.1 CCDS1703.1 Transcript intron_variant - - - - - - rs562956 2:21241454 T ENSESTG00000012930 ENSESTT00000032417 Transcript downstream_gene_variant - - - - - - DISTANCE=4941 rs562956 2:21241454 T ENSESTG00000012933 ENSESTT00000032436 Transcript intron_variant - - - - - - rs622236 2:21294509 T - - - intergenic_variant - - - - - - rs549137 2:21318050 G - - - intergenic_variant - - - - - - rs312943 2:21322853 A - - - intergenic_variant - - - - - - rs1652415 2:21407768 A - - - intergenic_variant - - - - - - rs2117300 2:21610265 C - - - intergenic_variant - - - - - - rs7579134 2:21753873 A - - - intergenic_variant - - - - - - rs6547786 2:21860472 C - - - intergenic_variant - - - - - - rs329784 2:22151826 A - - - intergenic_variant - - - - - - rs2460415 2:22166498 C ENSESTG00000004322 ENSESTT00000010901 Transcript downstream_gene_variant - - - - - - DISTANCE=983 rs7569335 2:22984559 C - - - intergenic_variant - - - - - - rs6711378 2:23037467 C - - - intergenic_variant - - - - - - rs6722249 2:23465042 C - - - intergenic_variant - - - - - - rs2723092 2:23546049 G - - - intergenic_variant - - - - - - rs2577719 2:23560398 C - - - intergenic_variant - - - - - - rs7579201 2:24108652 C ENSESTG00000025849 ENSESTT00000065156 Transcript missense_variant 161 134 45 Q/R cAg/cGg - rs7579201 2:24108652 C 54454 NM_017552.2 Transcript missense_variant 916 620 207 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs7579201 2:24108652 C 54454 NM_001242338.1 Transcript missense_variant 916 620 207 Q/R cAg/cGg - rs7579201 2:24108652 C CCDS46227.1 CCDS46227.1 Transcript missense_variant 620 620 207 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs7579201 2:24108652 C ENSESTG00000025839 ENSESTT00000065118 Transcript downstream_gene_variant - - - - - - DISTANCE=2568 rs12713091 2:24110164 T ENSESTG00000025849 ENSESTT00000065156 Transcript intron_variant - - - - - - rs12713091 2:24110164 T 54454 NM_017552.2 Transcript intron_variant - - - - - - rs12713091 2:24110164 T 54454 NM_001242338.1 Transcript intron_variant - - - - - - rs12713091 2:24110164 T CCDS46227.1 CCDS46227.1 Transcript intron_variant - - - - - - rs12713091 2:24110164 T ENSESTG00000025839 ENSESTT00000065118 Transcript downstream_gene_variant - - - - - - DISTANCE=1056 rs2339885 2:24181521 T ENSESTG00000025033 ENSESTT00000063246 Transcript intron_variant - - - - - - rs2339885 2:24181521 T 165324 NM_181713.3 Transcript intron_variant - - - - - - rs2339885 2:24181521 T CCDS1704.1 CCDS1704.1 Transcript intron_variant - - - - - - rs2339885 2:24181521 T ENSESTG00000025033 ENSESTT00000063444 Transcript intron_variant - - - - - - rs6545220 2:24229494 A 388931 NM_001080473.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3459 rs6545220 2:24229494 A CCDS46228.1 CCDS46228.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3473 rs6545220 2:24229494 A ENSESTG00000025154 ENSESTT00000063507 Transcript upstream_gene_variant - - - - - - DISTANCE=3457 rs6752072 2:24238543 G - ENSR00000586623 RegulatoryFeature regulatory_region_variant - - - - - - rs6752072 2:24238543 G 388931 NM_001080473.1 Transcript intron_variant - - - - - - rs6752072 2:24238543 G CCDS46228.1 CCDS46228.1 Transcript intron_variant - - - - - - rs6752072 2:24238543 G ENSESTG00000025154 ENSESTT00000063507 Transcript intron_variant - - - - - - rs2111883 2:24289413 A ENSESTG00000025182 ENSESTT00000063611 Transcript downstream_gene_variant - - - - - - DISTANCE=2867 rs2111883 2:24289413 A CCDS33153.1 CCDS33153.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3480 rs2111883 2:24289413 A CCDS1707.1 CCDS1707.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1219 rs2111883 2:24289413 A 2281 NM_054033.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2862 rs2111883 2:24289413 A CCDS1706.1 CCDS1706.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3351 rs2111883 2:24289413 A 2281 NM_004116.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2862 rs2111883 2:24289413 A ENSESTG00000025774 ENSESTT00000065015 Transcript downstream_gene_variant - - - - - - DISTANCE=1752 rs2111883 2:24289413 A 51639 NM_016047.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1041 rs2111883 2:24289413 A ENSESTG00000025774 ENSESTT00000065002 Transcript downstream_gene_variant - - - - - - DISTANCE=1287 rs2111883 2:24289413 A ENSESTG00000025182 ENSESTT00000063576 Transcript downstream_gene_variant - - - - - - DISTANCE=2867 rs2111883 2:24289413 A ENSESTG00000025182 ENSESTT00000063539 Transcript downstream_gene_variant - - - - - - DISTANCE=2867 rs2111883 2:24289413 A ENSESTG00000025182 ENSESTT00000063564 Transcript downstream_gene_variant - - - - - - DISTANCE=2867 rs1582614 2:24329030 A - - - intergenic_variant - - - - - - rs2033651 2:25062414 G ENSESTG00000002944 ENSESTT00000007308 Transcript downstream_gene_variant - - - - - - DISTANCE=341 rs2033651 2:25062414 G ENSESTG00000002944 ENSESTT00000007318 Transcript downstream_gene_variant - - - - - - DISTANCE=414 rs2033651 2:25062414 G ENSESTG00000002954 ENSESTT00000007346 Transcript upstream_gene_variant - - - - - - DISTANCE=1074 rs2033651 2:25062414 G CCDS1715.1 CCDS1715.1 Transcript intron_variant - - - - - - rs2033651 2:25062414 G ENSESTG00000002944 ENSESTT00000007322 Transcript downstream_gene_variant - - - - - - DISTANCE=414 rs2033651 2:25062414 G ENSESTG00000002944 ENSESTT00000007328 Transcript downstream_gene_variant - - - - - - DISTANCE=414 rs2033651 2:25062414 G 109 NM_004036.3 Transcript intron_variant - - - - - - rs1595611 2:25212278 C 729723 NR_034113.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1595611 2:25212278 C ENSESTG00000002733 ENSESTT00000006800 Transcript intron_variant - - - - - - rs934614 2:25588125 A - - - intergenic_variant - - - - - - rs1465878 2:26203678 C ENSESTG00000020001 ENSESTT00000050116 Transcript upstream_gene_variant - - - - - - DISTANCE=6 rs1465878 2:26203678 C ENSESTG00000021145 ENSESTT00000053231 Transcript upstream_gene_variant - - - - - - DISTANCE=43 rs1465878 2:26203678 C ENSESTG00000021145 ENSESTT00000053216 Transcript upstream_gene_variant - - - - - - DISTANCE=43 rs1465878 2:26203678 C CCDS1719.1 CCDS1719.1 Transcript missense_variant 1109 1109 370 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs1465878 2:26203678 C 3797 NM_002254.6 Transcript missense_variant 1766 1109 370 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs4665307 2:26320771 A ENSESTG00000020010 ENSESTT00000050273 Transcript upstream_gene_variant - - - - - - DISTANCE=628 rs4665307 2:26320771 A 10890 NM_016131.4 Transcript intron_variant - - - - - - rs4665307 2:26320771 A ENSESTG00000020010 ENSESTT00000050208 Transcript intron_variant - - - - - - rs4665307 2:26320771 A CCDS1720.1 CCDS1720.1 Transcript intron_variant - - - - - - rs4665307 2:26320771 A ENSESTG00000020010 ENSESTT00000050246 Transcript upstream_gene_variant - - - - - - DISTANCE=628 rs4665307 2:26320771 A ENSESTG00000021135 ENSESTT00000053039 Transcript intron_variant - - - - - - rs4665307 2:26320771 A ENSESTG00000020010 ENSESTT00000050222 Transcript downstream_gene_variant - - - - - - DISTANCE=4051 rs7564333 2:26783778 A 9381 NM_194248.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2212 rs7564333 2:26783778 A ENSESTG00000020784 ENSESTT00000052099 Transcript upstream_gene_variant - - - - - - DISTANCE=2125 rs7564333 2:26783778 A CCDS42661.1 CCDS42661.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1703 rs7564333 2:26783778 A CCDS1725.1 CCDS1725.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2339 rs7564333 2:26783778 A 339778 NM_001105519.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1703 rs1465719 2:27032340 C - - - intergenic_variant - - - - - - rs556240 2:27113215 T ENSESTG00000003421 ENSESTT00000008657 Transcript intron_variant - - - - - - rs556240 2:27113215 T ENSESTG00000003421 ENSESTT00000008650 Transcript intron_variant - - - - - - rs556240 2:27113215 T ENSESTG00000003421 ENSESTT00000008645 Transcript intron_variant - - - - - - rs556240 2:27113215 T 56896 NM_001253723.1 Transcript intron_variant - - - - - - rs556240 2:27113215 T ENSESTG00000003421 ENSESTT00000008655 Transcript intron_variant - - - - - - rs556240 2:27113215 T ENSESTG00000003421 ENSESTT00000008558 Transcript intron_variant - - - - - - rs556240 2:27113215 T ENSESTG00000003421 ENSESTT00000008648 Transcript intron_variant - - - - - - rs556240 2:27113215 T 56896 NM_020134.3 Transcript intron_variant - - - - - - rs556240 2:27113215 T ENSESTG00000003421 ENSESTT00000008642 Transcript intron_variant - - - - - - rs556240 2:27113215 T 56896 NM_001253724.1 Transcript intron_variant - - - - - - rs7562823 2:28277567 T ENSESTG00000014159 ENSESTT00000035477 Transcript intron_variant - - - - - - rs7562823 2:28277567 T CCDS1764.1 CCDS1764.1 Transcript intron_variant - - - - - - rs7562823 2:28277567 T 9577 NM_001261840.1 Transcript intron_variant - - - - - - rs7562823 2:28277567 T 9577 NM_199193.2 Transcript intron_variant - - - - - - rs7562823 2:28277567 T 9577 NM_199191.2 Transcript intron_variant - - - - - - rs7562823 2:28277567 T CCDS1765.1 CCDS1765.1 Transcript intron_variant - - - - - - rs7562823 2:28277567 T 9577 NM_004899.4 Transcript intron_variant - - - - - - rs7562823 2:28277567 T ENSESTG00000014159 ENSESTT00000035464 Transcript intron_variant - - - - - - rs7562823 2:28277567 T 9577 NM_199192.2 Transcript intron_variant - - - - - - rs7562823 2:28277567 T 9577 NM_199194.2 Transcript intron_variant - - - - - - rs7562823 2:28277567 T CCDS1763.1 CCDS1763.1 Transcript intron_variant - - - - - - rs4666037 2:28360640 C ENSESTG00000014159 ENSESTT00000035477 Transcript intron_variant - - - - - - rs4666037 2:28360640 C CCDS1764.1 CCDS1764.1 Transcript intron_variant - - - - - - rs4666037 2:28360640 C 9577 NM_001261840.1 Transcript intron_variant - - - - - - rs4666037 2:28360640 C 9577 NM_199193.2 Transcript intron_variant - - - - - - rs4666037 2:28360640 C 9577 NM_199191.2 Transcript intron_variant - - - - - - rs4666037 2:28360640 C CCDS1765.1 CCDS1765.1 Transcript intron_variant - - - - - - rs4666037 2:28360640 C 9577 NM_004899.4 Transcript intron_variant - - - - - - rs4666037 2:28360640 C ENSESTG00000014159 ENSESTT00000035464 Transcript intron_variant - - - - - - rs4666037 2:28360640 C 9577 NM_199192.2 Transcript intron_variant - - - - - - rs4666037 2:28360640 C 9577 NM_199194.2 Transcript intron_variant - - - - - - rs4666037 2:28360640 C CCDS1763.1 CCDS1763.1 Transcript intron_variant - - - - - - rs6725130 2:28391329 G - ENSR00001540666 RegulatoryFeature regulatory_region_variant - - - - - - rs6725130 2:28391329 G ENSESTG00000014159 ENSESTT00000035477 Transcript intron_variant - - - - - - rs6725130 2:28391329 G CCDS1764.1 CCDS1764.1 Transcript intron_variant - - - - - - rs6725130 2:28391329 G 9577 NM_001261840.1 Transcript intron_variant - - - - - - rs6725130 2:28391329 G 9577 NM_199193.2 Transcript intron_variant - - - - - - rs6725130 2:28391329 G ENSESTG00000014263 ENSESTT00000035703 Transcript intron_variant - - - - - - rs6725130 2:28391329 G 9577 NM_199191.2 Transcript intron_variant - - - - - - rs6725130 2:28391329 G CCDS1765.1 CCDS1765.1 Transcript intron_variant - - - - - - rs6725130 2:28391329 G 9577 NM_004899.4 Transcript intron_variant - - - - - - rs6725130 2:28391329 G ENSESTG00000014159 ENSESTT00000035464 Transcript intron_variant - - - - - - rs6725130 2:28391329 G 9577 NM_199192.2 Transcript intron_variant - - - - - - rs6725130 2:28391329 G 9577 NM_199194.2 Transcript intron_variant - - - - - - rs6725130 2:28391329 G CCDS1763.1 CCDS1763.1 Transcript intron_variant - - - - - - rs1534543 2:29560246 C - ENSR00001540799 RegulatoryFeature regulatory_region_variant - - - - - - rs1534543 2:29560246 C CCDS33172.1 CCDS33172.1 Transcript intron_variant - - - - - - rs1534543 2:29560246 C 238 NM_004304.4 Transcript intron_variant - - - - - - rs2631996 2:29868960 G CCDS33172.1 CCDS33172.1 Transcript intron_variant - - - - - - rs2631996 2:29868960 G 238 NM_004304.4 Transcript intron_variant - - - - - - rs2339528 2:29892205 T CCDS33172.1 CCDS33172.1 Transcript intron_variant - - - - - - rs2339528 2:29892205 T 238 NM_004304.4 Transcript intron_variant - - - - - - rs1374725 2:30316428 G ENSESTG00000035281 ENSESTT00000089098 Transcript intron_variant - - - - - - rs829572 2:30683204 T ENSESTG00000035267 ENSESTT00000089068 Transcript intron_variant - - - - - - rs829572 2:30683204 T ENSESTG00000035272 ENSESTT00000089080 Transcript intron_variant - - - - - - rs829572 2:30683204 T 253558 NM_001002257.1 Transcript intron_variant - - - - - - rs829572 2:30683204 T 253558 NM_182551.3 Transcript intron_variant - - - - - - rs829572 2:30683204 T ENSESTG00000035267 ENSESTT00000089078 Transcript intron_variant - - - - - - rs829572 2:30683204 T ENSESTG00000035267 ENSESTT00000089076 Transcript intron_variant - - - - - - rs829572 2:30683204 T CCDS1772.1 CCDS1772.1 Transcript intron_variant - - - - - - rs829572 2:30683204 T ENSESTG00000035267 ENSESTT00000089071 Transcript intron_variant - - - - - - rs1348438 2:31372763 G ENSESTG00000024926 ENSESTT00000062942 Transcript upstream_gene_variant - - - - - - DISTANCE=2919 rs207402 2:31531494 G - - - intergenic_variant - - - - - - rs477626 2:31609448 C ENSESTG00000024808 ENSESTT00000062665 Transcript downstream_gene_variant - - - - - - DISTANCE=1274 rs477626 2:31609448 C ENSESTG00000024808 ENSESTT00000062723 Transcript intron_variant - - - - - - rs477626 2:31609448 C CCDS1775.1 CCDS1775.1 Transcript intron_variant - - - - - - rs477626 2:31609448 C 7498 NM_000379.3 Transcript intron_variant - - - - - - rs206830 2:31704908 T - - - intergenic_variant - - - - - - rs401119 2:31729710 A - - - intergenic_variant - - - - - - rs2208531 2:31765627 G 6716 NM_000348.3 Transcript intron_variant - - - - - - rs2208531 2:31765627 G ENSESTG00000024763 ENSESTT00000062625 Transcript intron_variant - - - - - - rs11124263 2:31771477 T 6716 NM_000348.3 Transcript intron_variant - - - - - - rs11124263 2:31771477 T ENSESTG00000024763 ENSESTT00000062625 Transcript intron_variant - - - - - - rs1118795 2:31797509 A 6716 NM_000348.3 Transcript intron_variant - - - - - - rs1118795 2:31797509 A ENSESTG00000024763 ENSESTT00000062625 Transcript intron_variant - - - - - - rs2666408 2:31803579 T 6716 NM_000348.3 Transcript intron_variant - - - - - - rs2666408 2:31803579 T ENSESTG00000024763 ENSESTT00000062625 Transcript intron_variant - - - - - - rs494302 2:31804876 G 6716 NM_000348.3 Transcript intron_variant - - - - - - rs494302 2:31804876 G ENSESTG00000024763 ENSESTT00000062625 Transcript intron_variant - - - - - - rs619857 2:31805619 C - ENSR00000587667 RegulatoryFeature regulatory_region_variant - - - - - - rs619857 2:31805619 C 6716 NM_000348.3 Transcript intron_variant - - - - - - rs619857 2:31805619 C ENSESTG00000024763 ENSESTT00000062625 Transcript intron_variant - - - - - - rs675222 2:31808820 T 6716 NM_000348.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2780 rs675222 2:31808820 T ENSESTG00000024763 ENSESTT00000062625 Transcript upstream_gene_variant - - - - - - DISTANCE=2810 rs510829 2:31808862 G 6716 NM_000348.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2822 rs510829 2:31808862 G ENSESTG00000024763 ENSESTT00000062625 Transcript upstream_gene_variant - - - - - - DISTANCE=2852 rs3918525 2:31868980 T - - - intergenic_variant - - - - - - rs1265315 2:32568239 A - ENSR00000587732 RegulatoryFeature regulatory_region_variant - - - - - - rs1265315 2:32568239 A - - - intergenic_variant - - - - - - rs176402 2:32637837 T 57448 NM_016252.3 Transcript intron_variant - - - - - - rs176402 2:32637837 T ENSESTG00000016240 ENSESTT00000040758 Transcript upstream_gene_variant - - - - - - DISTANCE=3120 rs176402 2:32637837 T CCDS33175.2 CCDS33175.2 Transcript intron_variant - - - - - - rs176402 2:32637837 T ENSESTG00000016217 ENSESTT00000040739 Transcript intron_variant - - - - - - rs176402 2:32637837 T ENSESTG00000016217 ENSESTT00000040734 Transcript intron_variant - - - - - - rs11684262 2:32665817 T 57448 NM_016252.3 Transcript intron_variant - - - - - - rs11684262 2:32665817 T ENSESTG00000016240 ENSESTT00000040801 Transcript intron_variant - - - - - - rs11684262 2:32665817 T ENSESTG00000016240 ENSESTT00000040807 Transcript intron_variant - - - - - - rs11684262 2:32665817 T CCDS33175.2 CCDS33175.2 Transcript intron_variant - - - - - - rs11684262 2:32665817 T ENSESTG00000016240 ENSESTT00000040815 Transcript upstream_gene_variant - - - - - - DISTANCE=2677 rs60197615 2:32667182 C - ENSR00000587744 RegulatoryFeature regulatory_region_variant - - - - - - rs60197615 2:32667182 C 57448 NM_016252.3 Transcript missense_variant 4128 3994 1332 V/L Gtt/Ctt - PolyPhen=benign;SIFT=tolerated rs60197615 2:32667182 C ENSESTG00000016240 ENSESTT00000040801 Transcript missense_variant 652 607 203 V/L Gtt/Ctt - rs60197615 2:32667182 C ENSESTG00000016240 ENSESTT00000040807 Transcript missense_variant 612 526 176 V/L Gtt/Ctt - rs60197615 2:32667182 C CCDS33175.2 CCDS33175.2 Transcript missense_variant 3994 3994 1332 V/L Gtt/Ctt - PolyPhen=benign;SIFT=tolerated rs60197615 2:32667182 C ENSESTG00000016240 ENSESTT00000040815 Transcript upstream_gene_variant - - - - - - DISTANCE=1312 rs4952214 2:32696502 G 57448 NM_016252.3 Transcript intron_variant - - - - - - rs4952214 2:32696502 G ENSESTG00000016493 ENSESTT00000041525 Transcript upstream_gene_variant - - - - - - DISTANCE=4865 rs4952214 2:32696502 G ENSESTG00000016493 ENSESTT00000041513 Transcript upstream_gene_variant - - - - - - DISTANCE=4865 rs4952214 2:32696502 G CCDS33175.2 CCDS33175.2 Transcript intron_variant - - - - - - rs4952214 2:32696502 G ENSESTG00000016493 ENSESTT00000041374 Transcript intron_variant - - - - - - rs4952214 2:32696502 G ENSESTG00000016454 ENSESTT00000041297 Transcript downstream_gene_variant - - - - - - DISTANCE=2737 rs4952214 2:32696502 G ENSESTG00000016493 ENSESTT00000041379 Transcript intron_variant - - - - - - rs1980641 2:32700472 G 57448 NM_016252.3 Transcript intron_variant - - - - - - rs1980641 2:32700472 G ENSESTG00000016493 ENSESTT00000041525 Transcript upstream_gene_variant - - - - - - DISTANCE=895 rs1980641 2:32700472 G ENSESTG00000016493 ENSESTT00000041513 Transcript upstream_gene_variant - - - - - - DISTANCE=895 rs1980641 2:32700472 G CCDS33175.2 CCDS33175.2 Transcript intron_variant - - - - - - rs1980641 2:32700472 G ENSESTG00000016493 ENSESTT00000041532 Transcript upstream_gene_variant - - - - - - DISTANCE=2018 rs1980641 2:32700472 G ENSESTG00000016493 ENSESTT00000041374 Transcript intron_variant - - - - - - rs1980641 2:32700472 G ENSESTG00000016493 ENSESTT00000041379 Transcript downstream_gene_variant - - - - - - DISTANCE=2272 rs2366891 2:32712875 C 57448 NM_016252.3 Transcript splice_region_variant,intron_variant - - - - - - rs2366891 2:32712875 C ENSESTG00000016493 ENSESTT00000041525 Transcript splice_region_variant,intron_variant - - - - - - rs2366891 2:32712875 C ENSESTG00000016493 ENSESTT00000041513 Transcript splice_region_variant,intron_variant - - - - - - rs2366891 2:32712875 C CCDS33175.2 CCDS33175.2 Transcript splice_region_variant,intron_variant - - - - - - rs10181212 2:32746820 T 57448 NM_016252.3 Transcript intron_variant - - - - - - rs10181212 2:32746820 T CCDS33175.2 CCDS33175.2 Transcript intron_variant - - - - - - rs10181212 2:32746820 T ENSESTG00000016493 ENSESTT00000041761 Transcript intron_variant - - - - - - rs2710608 2:32749734 A 57448 NM_016252.3 Transcript intron_variant - - - - - - rs2710608 2:32749734 A CCDS33175.2 CCDS33175.2 Transcript intron_variant - - - - - - rs2710608 2:32749734 A ENSESTG00000016493 ENSESTT00000041761 Transcript intron_variant - - - - - - rs2754509 2:32758813 A 57448 NM_016252.3 Transcript intron_variant - - - - - - rs2754509 2:32758813 A CCDS33175.2 CCDS33175.2 Transcript intron_variant - - - - - - rs2754509 2:32758813 A 693143 NR_030285.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1500 rs2754509 2:32758813 A ENSESTG00000016493 ENSESTT00000041761 Transcript intron_variant - - - - - - rs2710620 2:32775231 T 57448 NM_016252.3 Transcript intron_variant - - - - - - rs2710620 2:32775231 T CCDS33175.2 CCDS33175.2 Transcript intron_variant - - - - - - rs2710620 2:32775231 T ENSESTG00000016493 ENSESTT00000041773 Transcript intron_variant - - - - - - rs2710620 2:32775231 T ENSESTG00000016493 ENSESTT00000041761 Transcript intron_variant - - - - - - rs10865092 2:33542069 A 4052 NM_000627.3 Transcript intron_variant - - - - - - rs10865092 2:33542069 A ENSESTG00000003114 ENSESTT00000007826 Transcript intron_variant - - - - - - rs10865092 2:33542069 A 4052 NM_001166265.1 Transcript intron_variant - - - - - - rs10865092 2:33542069 A 4052 NM_001166264.1 Transcript intron_variant - - - - - - rs10865092 2:33542069 A CCDS54345.1 CCDS54345.1 Transcript intron_variant - - - - - - rs10865092 2:33542069 A CCDS54344.1 CCDS54344.1 Transcript intron_variant - - - - - - rs10865092 2:33542069 A ENSESTG00000003114 ENSESTT00000007844 Transcript intron_variant - - - - - - rs10865092 2:33542069 A ENSESTG00000003114 ENSESTT00000007837 Transcript intron_variant - - - - - - rs10865092 2:33542069 A CCDS33178.2 CCDS33178.2 Transcript intron_variant - - - - - - rs10865092 2:33542069 A 4052 NM_001166266.1 Transcript intron_variant - - - - - - rs10865092 2:33542069 A CCDS33177.2 CCDS33177.2 Transcript intron_variant - - - - - - rs10865092 2:33542069 A ENSESTG00000003114 ENSESTT00000007829 Transcript intron_variant - - - - - - rs10865092 2:33542069 A 4052 NM_206943.2 Transcript intron_variant - - - - - - rs10865092 2:33542069 A ENSESTG00000003114 ENSESTT00000007821 Transcript intron_variant - - - - - - rs2080781 2:34462562 A - - - intergenic_variant - - - - - - rs10167127 2:34761717 C - - - intergenic_variant - - - - - - rs280703 2:35053715 A - - - intergenic_variant - - - - - - rs4670442 2:35367926 T - - - intergenic_variant - - - - - - rs1371416 2:35827563 A - - - intergenic_variant - - - - - - rs6543963 2:35876279 T - - - intergenic_variant - - - - - - rs10181454 2:35920560 G - - - intergenic_variant - - - - - - rs1510722 2:36306032 C - - - intergenic_variant - - - - - - rs10168116 2:37150642 A CCDS1784.1 CCDS1784.1 Transcript intron_variant - - - - - - rs10168116 2:37150642 A 6801 NM_003162.3 Transcript intron_variant - - - - - - rs10168116 2:37150642 A ENSESTG00000032165 ENSESTT00000081152 Transcript intron_variant - - - - - - rs7587520 2:37806839 C - - - intergenic_variant - - - - - - rs4670800 2:38179134 A ENSESTG00000031080 ENSESTT00000078301 Transcript intron_variant - - - - - - rs4670800 2:38179134 A ENSESTG00000031080 ENSESTT00000078298 Transcript intron_variant - - - - - - rs4670800 2:38179134 A ENSESTG00000031080 ENSESTT00000078279 Transcript intron_variant - - - - - - rs4670800 2:38179134 A ENSESTG00000031080 ENSESTT00000078291 Transcript intron_variant - - - - - - rs4670800 2:38179134 A 151393 NM_001170792.1 Transcript intron_variant - - - - - - rs4670800 2:38179134 A 151393 NM_144713.3 Transcript missense_variant 902 776 259 G/D gGt/gAt - PolyPhen=benign;SIFT=tolerated rs4670800 2:38179134 A CCDS1792.1 CCDS1792.1 Transcript missense_variant 776 776 259 G/D gGt/gAt - PolyPhen=benign;SIFT=tolerated rs4670800 2:38179134 A ENSESTG00000031080 ENSESTT00000078250 Transcript intron_variant - - - - - - rs4670800 2:38179134 A ENSESTG00000031080 ENSESTT00000078313 Transcript intron_variant - - - - - - rs4670800 2:38179134 A CCDS54351.1 CCDS54351.1 Transcript intron_variant - - - - - - rs4670800 2:38179134 A CCDS54352.1 CCDS54352.1 Transcript intron_variant - - - - - - rs4670800 2:38179134 A ENSESTG00000031124 ENSESTT00000078376 Transcript downstream_gene_variant - - - - - - DISTANCE=289 rs4670800 2:38179134 A 151393 NM_001170793.1 Transcript intron_variant - - - - - - rs4670800 2:38179134 A 151393 NM_001170791.1 Transcript intron_variant - - - - - - rs4670879 2:38757083 G - - - intergenic_variant - - - - - - rs3099954 2:39118205 G ENSESTG00000017293 ENSESTT00000043461 Transcript intron_variant - - - - - - rs1030037 2:39754368 G ENSESTG00000017362 ENSESTT00000043678 Transcript intron_variant - - - - - - rs1030037 2:39754368 G ENSESTG00000017362 ENSESTT00000043692 Transcript intron_variant - - - - - - rs1030037 2:39754368 G 728730 NR_037875.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1030037 2:39754368 G ENSESTG00000017362 ENSESTT00000043696 Transcript intron_variant - - - - - - rs2373703 2:40106139 A - - - intergenic_variant - - - - - - rs4952418 2:40732522 G ENSESTG00000015771 ENSESTT00000039488 Transcript intron_variant - - - - - - rs4952418 2:40732522 G 6546 NM_001112802.1 Transcript intron_variant - - - - - - rs9309085 2:42839406 G ENSESTG00000016721 ENSESTT00000042012 Transcript intron_variant - - - - - - rs9309085 2:42839406 G ENSESTG00000016721 ENSESTT00000042079 Transcript intron_variant - - - - - - rs9309085 2:42839406 G CCDS46267.1 CCDS46267.1 Transcript intron_variant - - - - - - rs9309085 2:42839406 G 57504 NM_020744.2 Transcript intron_variant - - - - - - rs9309085 2:42839406 G ENSESTG00000016721 ENSESTT00000042038 Transcript intron_variant - - - - - - rs9309085 2:42839406 G ENSESTG00000016721 ENSESTT00000042069 Transcript intron_variant - - - - - - rs9309085 2:42839406 G ENSESTG00000016721 ENSESTT00000042027 Transcript intron_variant - - - - - - rs9309085 2:42839406 G ENSESTG00000016721 ENSESTT00000042060 Transcript intron_variant - - - - - - rs10196260 2:43437924 C - ENSR00000300804 RegulatoryFeature regulatory_region_variant - - - - - - rs10196260 2:43437924 C - - - intergenic_variant - - - - - - rs6714691 2:43704312 C ENSESTG00000022908 ENSESTT00000058091 Transcript intron_variant - - - - - - rs6714691 2:43704312 C ENSESTG00000022908 ENSESTT00000058118 Transcript intron_variant - - - - - - rs6714691 2:43704312 C ENSESTG00000022908 ENSESTT00000058046 Transcript intron_variant - - - - - - rs6714691 2:43704312 C 63892 NM_001083953.1 Transcript intron_variant - - - - - - rs6714691 2:43704312 C ENSESTG00000022908 ENSESTT00000058072 Transcript intron_variant - - - - - - rs6714691 2:43704312 C 63892 NM_022065.4 Transcript intron_variant - - - - - - rs6714691 2:43704312 C ENSESTG00000022908 ENSESTT00000058103 Transcript intron_variant - - - - - - rs6714691 2:43704312 C CCDS46268.1 CCDS46268.1 Transcript intron_variant - - - - - - rs1907528 2:43750807 C ENSESTG00000022908 ENSESTT00000058091 Transcript intron_variant - - - - - - rs1907528 2:43750807 C ENSESTG00000022908 ENSESTT00000058103 Transcript intron_variant - - - - - - rs1907528 2:43750807 C ENSESTG00000022908 ENSESTT00000058046 Transcript intron_variant - - - - - - rs1907528 2:43750807 C 63892 NM_001083953.1 Transcript intron_variant - - - - - - rs1907528 2:43750807 C CCDS46268.1 CCDS46268.1 Transcript intron_variant - - - - - - rs1907528 2:43750807 C ENSESTG00000022908 ENSESTT00000058072 Transcript intron_variant - - - - - - rs1907528 2:43750807 C 63892 NM_022065.4 Transcript intron_variant - - - - - - rs6729304 2:44000223 C 51626 NM_001193464.1 Transcript upstream_gene_variant - - - - - - DISTANCE=955 rs6729304 2:44000223 C 51626 NM_016008.3 Transcript upstream_gene_variant - - - - - - DISTANCE=955 rs6729304 2:44000223 C ENSESTG00000018446 ENSESTT00000046579 Transcript upstream_gene_variant - - - - - - DISTANCE=977 rs6729304 2:44000223 C CCDS1813.1 CCDS1813.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1055 rs6729304 2:44000223 C CCDS46270.1 CCDS46270.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1055 rs6729304 2:44000223 C 51626 NM_015522.3 Transcript upstream_gene_variant - - - - - - DISTANCE=955 rs4414726 2:44241360 A - - - intergenic_variant - - - - - - rs2123777 2:44328288 G - - - intergenic_variant - - - - - - rs149466 2:45122268 A - ENSR00001541892 RegulatoryFeature regulatory_region_variant - - - - - - rs149466 2:45122268 A - - - intergenic_variant - - - - - - rs537012 2:45872763 G - - - intergenic_variant - - - - - - rs7598610 2:46234290 A ENSESTG00000014714 ENSESTT00000036902 Transcript intron_variant - - - - - - rs7598610 2:46234290 A 5581 NM_005400.2 Transcript intron_variant - - - - - - rs7598610 2:46234290 A ENSESTG00000014714 ENSESTT00000036870 Transcript intron_variant - - - - - - rs7598610 2:46234290 A ENSESTG00000014714 ENSESTT00000036898 Transcript intron_variant - - - - - - rs7598610 2:46234290 A ENSESTG00000014714 ENSESTT00000036857 Transcript intron_variant - - - - - - rs7598610 2:46234290 A CCDS1824.1 CCDS1824.1 Transcript intron_variant - - - - - - rs4633966 2:47289651 C ENSESTG00000028719 ENSESTT00000072753 Transcript intron_variant - - - - - - rs4633966 2:47289651 C ENSESTG00000028719 ENSESTT00000072619 Transcript intron_variant - - - - - - rs4633966 2:47289651 C CCDS33193.1 CCDS33193.1 Transcript intron_variant - - - - - - rs4633966 2:47289651 C ENSESTG00000029351 ENSESTT00000073901 Transcript downstream_gene_variant - - - - - - DISTANCE=3412 rs4633966 2:47289651 C ENSESTG00000029351 ENSESTT00000073875 Transcript intron_variant - - - - - - rs4633966 2:47289651 C 57217 NM_020458.2 Transcript intron_variant - - - - - - rs12052441 2:47310410 C 285051 NM_001163561.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3720 rs12052441 2:47310410 C ENSESTG00000029351 ENSESTT00000073890 Transcript intron_variant - - - - - - rs12052441 2:47310410 C CCDS54356.1 CCDS54356.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3737 rs12052441 2:47310410 C ENSESTG00000029351 ENSESTT00000073901 Transcript intron_variant - - - - - - rs12052441 2:47310410 C ENSESTG00000029351 ENSESTT00000073875 Transcript intron_variant - - - - - - rs1880582 2:47325332 C 285051 NM_001163561.1 Transcript intron_variant - - - - - - rs1880582 2:47325332 C ENSESTG00000029351 ENSESTT00000073890 Transcript intron_variant - - - - - - rs1880582 2:47325332 C CCDS54356.1 CCDS54356.1 Transcript intron_variant - - - - - - rs1880582 2:47325332 C ENSESTG00000029351 ENSESTT00000073901 Transcript intron_variant - - - - - - rs1880582 2:47325332 C ENSESTG00000029351 ENSESTT00000073875 Transcript intron_variant - - - - - - rs6544983 2:47561621 A - ENSR00000301035 RegulatoryFeature regulatory_region_variant - - - - - - rs6544983 2:47561621 A ENSESTG00000029229 ENSESTT00000073618 Transcript intron_variant - - - - - - rs6544983 2:47561621 A 618 NR_001568.1 Transcript upstream_gene_variant - - - - - - DISTANCE=833 rs1346070 2:47839769 T - - - intergenic_variant - - - - - - rs2348497 2:48122793 A ENSESTG00000002823 ENSESTT00000007102 Transcript intron_variant - - - - - - rs2348497 2:48122793 A ENSESTG00000002823 ENSESTT00000007096 Transcript intron_variant - - - - - - rs2348497 2:48122793 A ENSESTG00000002823 ENSESTT00000007105 Transcript intron_variant - - - - - - rs2348497 2:48122793 A CCDS54357.1 CCDS54357.1 Transcript intron_variant - - - - - - rs2348497 2:48122793 A 80204 NM_001190274.1 Transcript intron_variant - - - - - - rs2348497 2:48122793 A ENSESTG00000002823 ENSESTT00000007093 Transcript intron_variant - - - - - - rs2348497 2:48122793 A ENSESTG00000002823 ENSESTT00000007088 Transcript intron_variant - - - - - - rs4350799 2:48178737 C - - - intergenic_variant - - - - - - rs146517520 2:48189523 C - - - intergenic_variant - - - - - - rs6545007 2:48190558 G - - - intergenic_variant - - - - - - rs4953563 2:48430372 C - - - intergenic_variant - - - - - - rs7587886 2:48785837 T 11037 NM_006873.3 Transcript intron_variant - - - - - - rs7587886 2:48785837 T ENSESTG00000002799 ENSESTT00000006955 Transcript intron_variant - - - - - - rs7587886 2:48785837 T 11037 NM_001198595.1 Transcript intron_variant - - - - - - rs7587886 2:48785837 T 286749 NM_001198593.1 Transcript intron_variant - - - - - - rs7587886 2:48785837 T ENSESTG00000002799 ENSESTT00000006948 Transcript intron_variant - - - - - - rs6545056 2:48889584 T CCDS56119.1 CCDS56119.1 Transcript intron_variant - - - - - - rs6545056 2:48889584 T ENSESTG00000010091 ENSESTT00000025278 Transcript intron_variant - - - - - - rs6545056 2:48889584 T CCDS54359.1 CCDS54359.1 Transcript intron_variant - - - - - - rs6545056 2:48889584 T 286749 NM_172311.2 Transcript intron_variant - - - - - - rs6545056 2:48889584 T CCDS1840.1 CCDS1840.1 Transcript intron_variant - - - - - - rs6545056 2:48889584 T 11036 NM_006872.3 Transcript intron_variant - - - - - - rs6545056 2:48889584 T 286749 NM_001198594.1 Transcript intron_variant - - - - - - rs6545056 2:48889584 T CCDS56118.1 CCDS56118.1 Transcript intron_variant - - - - - - rs6545056 2:48889584 T CCDS46281.1 CCDS46281.1 Transcript intron_variant - - - - - - rs6545056 2:48889584 T 286749 NM_001198593.1 Transcript intron_variant - - - - - - rs6545056 2:48889584 T 11036 NM_001193487.1 Transcript intron_variant - - - - - - rs6545056 2:48889584 T ENSESTG00000010091 ENSESTT00000025269 Transcript intron_variant - - - - - - rs6733079 2:48935849 C CCDS56118.1 CCDS56118.1 Transcript intron_variant - - - - - - rs6733079 2:48935849 C ENSESTG00000010124 ENSESTT00000025341 Transcript downstream_gene_variant - - - - - - DISTANCE=61 rs6733079 2:48935849 C CCDS1842.1 CCDS1842.1 Transcript intron_variant - - - - - - rs6733079 2:48935849 C 286749 NM_001198593.1 Transcript intron_variant - - - - - - rs6733079 2:48935849 C ENSESTG00000010091 ENSESTT00000025278 Transcript intron_variant - - - - - - rs6733079 2:48935849 C ENSESTG00000010091 ENSESTT00000025269 Transcript intron_variant - - - - - - rs6733079 2:48935849 C 3973 NM_000233.3 Transcript intron_variant - - - - - - rs11125185 2:49085391 C - - - intergenic_variant - - - - - - rs2160146 2:49105987 G - - - intergenic_variant - - - - - - rs4971716 2:49436299 C - - - intergenic_variant - - - - - - rs1346338 2:49506381 C - - - intergenic_variant - - - - - - rs12475532 2:49517648 G - - - intergenic_variant - - - - - - rs1346339 2:49559718 G - - - intergenic_variant - - - - - - rs1559939 2:49825199 A - - - intergenic_variant - - - - - - rs75542327 2:49862096 G - - - intergenic_variant - - - - - - rs1865491 2:50105886 A - - - intergenic_variant - - - - - - rs6545146 2:50248242 C CCDS46282.1 CCDS46282.1 Transcript intron_variant - - - - - - rs6545146 2:50248242 C CCDS1845.1 CCDS1845.1 Transcript intron_variant - - - - - - rs6545146 2:50248242 C 9378 NM_004801.4 Transcript intron_variant - - - - - - rs6545146 2:50248242 C 9378 NM_138735.2 Transcript intron_variant - - - - - - rs6545146 2:50248242 C CCDS54360.1 CCDS54360.1 Transcript intron_variant - - - - - - rs6545146 2:50248242 C ENSESTG00000016613 ENSESTT00000041650 Transcript intron_variant - - - - - - rs6545146 2:50248242 C 9378 NM_001135659.1 Transcript intron_variant - - - - - - rs967406 2:50361138 T CCDS46282.1 CCDS46282.1 Transcript intron_variant - - - - - - rs967406 2:50361138 T CCDS1845.1 CCDS1845.1 Transcript intron_variant - - - - - - rs967406 2:50361138 T 9378 NM_004801.4 Transcript intron_variant - - - - - - rs967406 2:50361138 T 9378 NM_138735.2 Transcript intron_variant - - - - - - rs967406 2:50361138 T CCDS54360.1 CCDS54360.1 Transcript intron_variant - - - - - - rs967406 2:50361138 T 9378 NM_001135659.1 Transcript intron_variant - - - - - - rs12713102 2:50698995 C CCDS46282.1 CCDS46282.1 Transcript intron_variant - - - - - - rs12713102 2:50698995 C 9378 NM_004801.4 Transcript intron_variant - - - - - - rs12713102 2:50698995 C CCDS54360.1 CCDS54360.1 Transcript intron_variant - - - - - - rs12713102 2:50698995 C 9378 NM_001135659.1 Transcript intron_variant - - - - - - rs2216173 2:50761052 C ENSESTG00000016574 ENSESTT00000041592 Transcript intron_variant - - - - - - rs2216173 2:50761052 C CCDS46282.1 CCDS46282.1 Transcript intron_variant - - - - - - rs2216173 2:50761052 C ENSESTG00000016574 ENSESTT00000041616 Transcript intron_variant - - - - - - rs2216173 2:50761052 C 9378 NM_004801.4 Transcript intron_variant - - - - - - rs2216173 2:50761052 C CCDS54360.1 CCDS54360.1 Transcript intron_variant - - - - - - rs2216173 2:50761052 C 9378 NM_001135659.1 Transcript intron_variant - - - - - - rs2216173 2:50761052 C ENSESTG00000016574 ENSESTT00000041606 Transcript intron_variant - - - - - - rs728393 2:51066301 T CCDS46282.1 CCDS46282.1 Transcript intron_variant - - - - - - rs728393 2:51066301 T 9378 NM_004801.4 Transcript intron_variant - - - - - - rs728393 2:51066301 T CCDS54360.1 CCDS54360.1 Transcript intron_variant - - - - - - rs728393 2:51066301 T 9378 NM_001135659.1 Transcript intron_variant - - - - - - rs2193415 2:51164149 G CCDS46282.1 CCDS46282.1 Transcript intron_variant - - - - - - rs2193415 2:51164149 G ENSESTG00000021889 ENSESTT00000055103 Transcript intron_variant - - - - - - rs2193415 2:51164149 G 9378 NM_004801.4 Transcript intron_variant - - - - - - rs2193415 2:51164149 G CCDS54360.1 CCDS54360.1 Transcript intron_variant - - - - - - rs2193415 2:51164149 G 9378 NM_001135659.1 Transcript intron_variant - - - - - - rs12713127 2:51192230 A CCDS46282.1 CCDS46282.1 Transcript intron_variant - - - - - - rs12713127 2:51192230 A ENSESTG00000021889 ENSESTT00000055103 Transcript intron_variant - - - - - - rs12713127 2:51192230 A 9378 NM_004801.4 Transcript intron_variant - - - - - - rs12713127 2:51192230 A CCDS54360.1 CCDS54360.1 Transcript intron_variant - - - - - - rs12713127 2:51192230 A 9378 NM_001135659.1 Transcript intron_variant - - - - - - rs10169858 2:51192878 T CCDS46282.1 CCDS46282.1 Transcript intron_variant - - - - - - rs10169858 2:51192878 T ENSESTG00000021889 ENSESTT00000055103 Transcript intron_variant - - - - - - rs10169858 2:51192878 T 9378 NM_004801.4 Transcript intron_variant - - - - - - rs10169858 2:51192878 T CCDS54360.1 CCDS54360.1 Transcript intron_variant - - - - - - rs10169858 2:51192878 T 9378 NM_001135659.1 Transcript intron_variant - - - - - - rs6723025 2:51369132 A - - - intergenic_variant - - - - - - rs2160648 2:51418069 T - - - intergenic_variant - - - - - - rs1005738 2:51424015 C - - - intergenic_variant - - - - - - rs13004205 2:51517251 C - - - intergenic_variant - - - - - - rs6744367 2:51520870 A - - - intergenic_variant - - - - - - rs6732403 2:51568891 C - - - intergenic_variant - - - - - - rs1188250 2:52033392 G - - - intergenic_variant - - - - - - rs2117829 2:52053651 A - - - intergenic_variant - - - - - - rs984813 2:52162507 C - - - intergenic_variant - - - - - - rs350798 2:52913819 C - - - intergenic_variant - - - - - - rs350790 2:52939169 T - - - intergenic_variant - - - - - - rs1454404 2:52953706 T ENSESTG00000002043 ENSESTT00000005081 Transcript intron_variant - - - - - - rs1454404 2:52953706 T ENSESTG00000002043 ENSESTT00000005086 Transcript intron_variant - - - - - - rs1818410 2:53138970 G - - - intergenic_variant - - - - - - rs6761774 2:53913865 T 51130 NM_145863.2 Transcript intron_variant - - - - - - rs6761774 2:53913865 T CCDS1847.1 CCDS1847.1 Transcript intron_variant - - - - - - rs6761774 2:53913865 T 100302652 NM_001164165.1 Transcript intron_variant - - - - - - rs6761774 2:53913865 T 51130 NM_016115.4 Transcript intron_variant - - - - - - rs6761774 2:53913865 T CCDS1846.1 CCDS1846.1 Transcript intron_variant - - - - - - rs6761774 2:53913865 T ENSESTG00000021483 ENSESTT00000053897 Transcript intron_variant - - - - - - rs6761774 2:53913865 T 51130 NM_001201965.1 Transcript intron_variant - - - - - - rs6761774 2:53913865 T CCDS54361.1 CCDS54361.1 Transcript intron_variant - - - - - - rs4671919 2:54620547 A - - - intergenic_variant - - - - - - rs3951716 2:54635431 G - - - intergenic_variant - - - - - - rs149381 2:55011747 G 400954 NM_001039753.2 Transcript intron_variant - - - - - - rs149381 2:55011747 G CCDS46286.1 CCDS46286.1 Transcript intron_variant - - - - - - rs149381 2:55011747 G ENSESTG00000017314 ENSESTT00000043526 Transcript intron_variant - - - - - - rs149381 2:55011747 G ENSESTG00000017314 ENSESTT00000043514 Transcript intron_variant - - - - - - rs782581 2:55917978 A ENSESTG00000013705 ENSESTT00000034316 Transcript intron_variant - - - - - - rs782581 2:55917978 A 87178 NM_033109.3 Transcript intron_variant - - - - - - rs782581 2:55917978 A CCDS1856.1 CCDS1856.1 Transcript intron_variant - - - - - - rs782581 2:55917978 A ENSESTG00000013705 ENSESTT00000034368 Transcript intron_variant - - - - - - rs782581 2:55917978 A ENSESTG00000013705 ENSESTT00000034345 Transcript intron_variant - - - - - - rs782581 2:55917978 A ENSESTG00000013705 ENSESTT00000034339 Transcript intron_variant - - - - - - rs782581 2:55917978 A ENSESTG00000013705 ENSESTT00000034340 Transcript intron_variant - - - - - - rs2868991 2:56309614 C ENSESTG00000013651 ENSESTT00000034145 Transcript intron_variant - - - - - - rs6545556 2:56413121 G - ENSR00000013269 RegulatoryFeature regulatory_region_variant - - - - - - rs6545556 2:56413121 G CCDS46290.1 CCDS46290.1 Transcript intron_variant - - - - - - rs6545556 2:56413121 G ENSESTG00000013643 ENSESTT00000034124 Transcript intron_variant - - - - - - rs6545556 2:56413121 G ENSESTG00000013648 ENSESTT00000034140 Transcript upstream_gene_variant - - - - - - DISTANCE=1078 rs6545556 2:56413121 G 114800 NM_001080433.1 Transcript intron_variant - - - - - - rs6545556 2:56413121 G ENSESTG00000013648 ENSESTT00000034136 Transcript upstream_gene_variant - - - - - - DISTANCE=216 rs214035 2:56540932 T CCDS46290.1 CCDS46290.1 Transcript intron_variant - - - - - - rs214035 2:56540932 T 114800 NM_001080433.1 Transcript intron_variant - - - - - - rs4672137 2:56793800 A - - - intergenic_variant - - - - - - rs4672161 2:56991042 T - - - intergenic_variant - - - - - - rs6749566 2:57364826 A - - - intergenic_variant - - - - - - rs7595936 2:57480448 G - - - intergenic_variant - - - - - - rs6760071 2:58738445 C ENSESTG00000031121 ENSESTT00000078379 Transcript intron_variant - - - - - - rs6760071 2:58738445 C ENSESTG00000031121 ENSESTT00000078367 Transcript intron_variant - - - - - - rs6545706 2:59090620 A ENSESTG00000027407 ENSESTT00000069066 Transcript intron_variant - - - - - - rs6545706 2:59090620 A 400955 NR_033873.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6545706 2:59090620 A ENSESTG00000031121 ENSESTT00000078367 Transcript intron_variant - - - - - - rs4672275 2:59247352 C ENSESTG00000027407 ENSESTT00000069066 Transcript intron_variant - - - - - - rs4672275 2:59247352 C 400955 NR_033873.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2110476 2:59335622 C - - - intergenic_variant - - - - - - rs2192572 2:59533908 T ENSESTG00000027466 ENSESTT00000069141 Transcript intron_variant - - - - - - rs2192609 2:59698539 C - - - intergenic_variant - - - - - - rs7574898 2:60083923 C - - - intergenic_variant - - - - - - rs970845 2:60384115 G - - - intergenic_variant - - - - - - rs243031 2:60605592 T ENSESTG00000030165 ENSESTT00000075911 Transcript intron_variant - - - - - - rs243031 2:60605592 T ENSESTG00000030165 ENSESTT00000075895 Transcript intron_variant - - - - - - rs759448 2:60659146 A - - - intergenic_variant - - - - - - rs1012584 2:60671582 C - - - intergenic_variant - - - - - - rs356981 2:60795134 A - - - intergenic_variant - - - - - - rs13018013 2:61968705 G - - - intergenic_variant - - - - - - rs2665640 2:62965145 C CCDS1872.1 CCDS1872.1 Transcript intron_variant - - - - - - rs2665640 2:62965145 C 23301 NM_001142615.2 Transcript intron_variant - - - - - - rs2665640 2:62965145 C 23301 NM_001142614.1 Transcript intron_variant - - - - - - rs2665640 2:62965145 C ENSESTG00000016895 ENSESTT00000042493 Transcript intron_variant - - - - - - rs2665640 2:62965145 C ENSESTG00000016895 ENSESTT00000042520 Transcript intron_variant - - - - - - rs2665640 2:62965145 C CCDS46300.1 CCDS46300.1 Transcript intron_variant - - - - - - rs2665640 2:62965145 C CCDS46299.1 CCDS46299.1 Transcript intron_variant - - - - - - rs2665640 2:62965145 C 23301 NM_001142616.1 Transcript intron_variant - - - - - - rs2665640 2:62965145 C 23301 NM_015252.3 Transcript intron_variant - - - - - - rs2098306 2:63133490 T CCDS1872.1 CCDS1872.1 Transcript intron_variant - - - - - - rs2098306 2:63133490 T 23301 NM_001142615.2 Transcript intron_variant - - - - - - rs2098306 2:63133490 T 23301 NM_001142614.1 Transcript intron_variant - - - - - - rs2098306 2:63133490 T CCDS46300.1 CCDS46300.1 Transcript intron_variant - - - - - - rs2098306 2:63133490 T 23301 NM_001142616.1 Transcript intron_variant - - - - - - rs2098306 2:63133490 T CCDS46299.1 CCDS46299.1 Transcript intron_variant - - - - - - rs2098306 2:63133490 T ENSESTG00000016968 ENSESTT00000042558 Transcript intron_variant - - - - - - rs2098306 2:63133490 T 23301 NM_015252.3 Transcript intron_variant - - - - - - rs262522 2:63892629 C - - - intergenic_variant - - - - - - rs4233929 2:63995153 A - - - intergenic_variant - - - - - - rs10221964 2:64241416 T ENSESTG00000003500 ENSESTT00000008731 Transcript intron_variant - - - - - - rs10221964 2:64241416 T 51542 NM_001005739.1 Transcript intron_variant - - - - - - rs10221964 2:64241416 T 51542 NM_016516.2 Transcript intron_variant - - - - - - rs10221964 2:64241416 T ENSESTG00000003500 ENSESTT00000008742 Transcript intron_variant - - - - - - rs2581041 2:64278849 A - - - intergenic_variant - - - - - - rs2919223 2:64309859 A - - - intergenic_variant - - - - - - rs12713528 2:65179207 G - - - intergenic_variant - - - - - - rs7559886 2:65247805 T ENSESTG00000009938 ENSESTT00000024938 Transcript intron_variant - - - - - - rs7559886 2:65247805 T 6509 NM_003038.4 Transcript intron_variant - - - - - - rs7559886 2:65247805 T CCDS1879.1 CCDS1879.1 Transcript intron_variant - - - - - - rs7559886 2:65247805 T ENSESTG00000009938 ENSESTT00000024907 Transcript intron_variant - - - - - - rs7559886 2:65247805 T ENSESTG00000009938 ENSESTT00000024940 Transcript intron_variant - - - - - - rs7559886 2:65247805 T 6509 NM_001193493.1 Transcript intron_variant - - - - - - rs7559886 2:65247805 T ENSESTG00000009938 ENSESTT00000024945 Transcript intron_variant - - - - - - rs7559886 2:65247805 T CCDS54362.1 CCDS54362.1 Transcript intron_variant - - - - - - rs759457 2:65292382 T - ENSR00001543019 RegulatoryFeature regulatory_region_variant - - - - - - rs759457 2:65292382 T ENSESTG00000009994 ENSESTT00000025011 Transcript upstream_gene_variant - - - - - - DISTANCE=4507 rs759457 2:65292382 T ENSESTG00000009994 ENSESTT00000025002 Transcript upstream_gene_variant - - - - - - DISTANCE=4449 rs759457 2:65292382 T ENSESTG00000009994 ENSESTT00000024998 Transcript intron_variant - - - - - - rs759457 2:65292382 T CCDS1880.2 CCDS1880.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4197 rs759457 2:65292382 T ENSESTG00000009994 ENSESTT00000024999 Transcript intron_variant - - - - - - rs759457 2:65292382 T 23177 NM_015147.2 Transcript intron_variant - - - - - - rs6546126 2:65343453 G 5861 NM_015543.1 Transcript intron_variant - - - - - - rs6546126 2:65343453 G CCDS46306.1 CCDS46306.1 Transcript intron_variant - - - - - - rs6546126 2:65343453 G ENSESTG00000010067 ENSESTT00000025218 Transcript intron_variant - - - - - - rs6546126 2:65343453 G 5861 NM_004161.4 Transcript intron_variant - - - - - - rs6546126 2:65343453 G CCDS46305.1 CCDS46305.1 Transcript intron_variant - - - - - - rs6546126 2:65343453 G ENSESTG00000010067 ENSESTT00000025223 Transcript intron_variant - - - - - - rs2043725 2:65677443 G - - - intergenic_variant - - - - - - rs1401452 2:66581448 A 100616464 NR_039938.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3933 rs1568321 2:66625862 A - - - intergenic_variant - - - - - - rs10201900 2:66652836 C - ENSR00000591885 RegulatoryFeature regulatory_region_variant - - - - - - rs10201900 2:66652836 C 730198 NR_046438.1 Transcript non_coding_exon_variant,nc_transcript_variant 1738 - - - - - rs6546252 2:66888476 G - - - intergenic_variant - - - - - - rs1125681 2:67050926 A - - - intergenic_variant - - - - - - rs4671827 2:67910525 C - - - intergenic_variant - - - - - - rs2195685 2:68001862 G - - - intergenic_variant - - - - - - rs6722075 2:69211631 C ENSESTG00000018119 ENSESTT00000045713 Transcript downstream_gene_variant - - - - - - DISTANCE=3525 rs6722075 2:69211631 C CCDS1891.2 CCDS1891.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3676 rs6722075 2:69211631 C 56287 NM_019617.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3519 rs4853275 2:70267280 T 400960 NR_033872.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs107514 2:70798962 C - - - intergenic_variant - - - - - - rs435280 2:70808004 C - - - intergenic_variant - - - - - - rs2192967 2:70936148 G - ENSR00001543438 RegulatoryFeature regulatory_region_variant - - - - - - rs2192967 2:70936148 G ENSESTG00000034121 ENSESTT00000086264 Transcript intron_variant - - - - - - rs2192967 2:70936148 G 119 NM_017488.3 Transcript intron_variant - - - - - - rs2192967 2:70936148 G 119 NM_001185055.1 Transcript intron_variant - - - - - - rs2192967 2:70936148 G CCDS54365.1 CCDS54365.1 Transcript intron_variant - - - - - - rs2192967 2:70936148 G 119 NM_001617.3 Transcript intron_variant - - - - - - rs2192967 2:70936148 G CCDS1909.1 CCDS1909.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2608 rs2192967 2:70936148 G 119 NM_001185054.1 Transcript intron_variant - - - - - - rs2192967 2:70936148 G ENSESTG00000034121 ENSESTT00000086271 Transcript intron_variant - - - - - - rs2192967 2:70936148 G CCDS46318.1 CCDS46318.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2608 rs2192967 2:70936148 G ENSESTG00000034121 ENSESTT00000086276 Transcript intron_variant - - - - - - rs2192967 2:70936148 G 119 NM_017482.3 Transcript intron_variant - - - - - - rs2192967 2:70936148 G CCDS1906.1 CCDS1906.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2608 rs988687 2:72010301 G - - - intergenic_variant - - - - - - rs898237 2:72021393 C - - - intergenic_variant - - - - - - rs991135 2:72194540 A - - - intergenic_variant - - - - - - rs520474 2:73472441 T ENSESTG00000034367 ENSESTT00000086969 Transcript intron_variant - - - - - - rs520474 2:73472441 T 10574 NM_001166284.1 Transcript intron_variant - - - - - - rs520474 2:73472441 T 10574 NM_001009570.2 Transcript intron_variant - - - - - - rs520474 2:73472441 T ENSESTG00000034367 ENSESTT00000086965 Transcript intron_variant - - - - - - rs520474 2:73472441 T CCDS54367.1 CCDS54367.1 Transcript intron_variant - - - - - - rs520474 2:73472441 T 10574 NM_006429.3 Transcript intron_variant - - - - - - rs520474 2:73472441 T 10574 NR_029403.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs520474 2:73472441 T ENSESTG00000034367 ENSESTT00000086990 Transcript intron_variant - - - - - - rs520474 2:73472441 T CCDS46336.1 CCDS46336.1 Transcript intron_variant - - - - - - rs520474 2:73472441 T ENSESTG00000034367 ENSESTT00000086959 Transcript intron_variant - - - - - - rs520474 2:73472441 T ENSESTG00000034367 ENSESTT00000087011 Transcript intron_variant - - - - - - rs520474 2:73472441 T CCDS54366.1 CCDS54366.1 Transcript intron_variant - - - - - - rs520474 2:73472441 T 10574 NM_001166285.1 Transcript intron_variant - - - - - - rs520474 2:73472441 T 10574 NR_029402.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs520474 2:73472441 T CCDS42696.1 CCDS42696.1 Transcript intron_variant - - - - - - rs205649 2:74898123 A CCDS1955.1 CCDS1955.1 Transcript intron_variant - - - - - - rs205649 2:74898123 A ENSESTG00000014632 ENSESTT00000036588 Transcript intron_variant - - - - - - rs205649 2:74898123 A ENSESTG00000014456 ENSESTT00000036207 Transcript intron_variant - - - - - - rs205649 2:74898123 A ENSESTG00000014456 ENSESTT00000036242 Transcript upstream_gene_variant - - - - - - DISTANCE=2792 rs205649 2:74898123 A ENSESTG00000014456 ENSESTT00000036220 Transcript intron_variant - - - - - - rs205649 2:74898123 A 10505 NM_004263.3 Transcript intron_variant - - - - - - rs1006936 2:75419638 T ENSESTG00000014616 ENSESTT00000036562 Transcript intron_variant - - - - - - rs1006936 2:75419638 T 6869 NM_001058.3 Transcript intron_variant - - - - - - rs1006936 2:75419638 T 6869 NM_015727.2 Transcript intron_variant - - - - - - rs1006936 2:75419638 T CCDS46345.1 CCDS46345.1 Transcript intron_variant - - - - - - rs1006936 2:75419638 T CCDS1958.1 CCDS1958.1 Transcript intron_variant - - - - - - rs2098308 2:75706672 G - - - intergenic_variant - - - - - - rs2588493 2:75764935 T ENSESTG00000014589 ENSESTT00000036513 Transcript intron_variant - - - - - - rs2588493 2:75764935 T ENSESTG00000014589 ENSESTT00000036518 Transcript intron_variant - - - - - - rs2588493 2:75764935 T 84141 NM_032181.2 Transcript intron_variant - - - - - - rs2588493 2:75764935 T ENSESTG00000014589 ENSESTT00000036530 Transcript intron_variant - - - - - - rs2588493 2:75764935 T ENSESTG00000014589 ENSESTT00000036506 Transcript intron_variant - - - - - - rs2588493 2:75764935 T ENSESTG00000014589 ENSESTT00000036501 Transcript intron_variant - - - - - - rs2588493 2:75764935 T ENSESTG00000014589 ENSESTT00000036527 Transcript intron_variant - - - - - - rs2588493 2:75764935 T 84141 NM_001135032.1 Transcript intron_variant - - - - - - rs2588493 2:75764935 T ENSESTG00000014589 ENSESTT00000036523 Transcript intron_variant - - - - - - rs7589577 2:75850630 A - - - intergenic_variant - - - - - - rs2692744 2:76213078 C - - - intergenic_variant - - - - - - rs317227 2:76226996 A - - - intergenic_variant - - - - - - rs11126502 2:76387982 C - - - intergenic_variant - - - - - - rs1215902 2:76538876 C - ENSR00000593237 RegulatoryFeature regulatory_region_variant - - - - - - rs1215902 2:76538876 C - - - intergenic_variant - - - - - - rs10445949 2:76661417 T - - - intergenic_variant - - - - - - rs6547086 2:76663515 G - - - intergenic_variant - - - - - - rs1439717 2:77388044 T CCDS46346.1 CCDS46346.1 Transcript intron_variant - - - - - - rs1439717 2:77388044 T 80059 NM_001134745.1 Transcript intron_variant - - - - - - rs2861053 2:77747417 C CCDS46346.1 CCDS46346.1 Transcript intron_variant - - - - - - rs2861053 2:77747417 C ENSESTG00000028967 ENSESTT00000073014 Transcript intron_variant - - - - - - rs2861053 2:77747417 C 80059 NM_024993.4 Transcript intron_variant - - - - - - rs2861053 2:77747417 C ENSESTG00000028967 ENSESTT00000072923 Transcript intron_variant - - - - - - rs2861053 2:77747417 C ENSESTG00000028967 ENSESTT00000073041 Transcript intron_variant - - - - - - rs2861053 2:77747417 C 80059 NM_001134745.1 Transcript intron_variant - - - - - - rs2861053 2:77747417 C CCDS46347.1 CCDS46347.1 Transcript intron_variant - - - - - - rs2861053 2:77747417 C ENSESTG00000028967 ENSESTT00000073002 Transcript intron_variant - - - - - - rs2060280 2:78122231 A ENSESTG00000028962 ENSESTT00000072883 Transcript intron_variant - - - - - - rs2218029 2:78291645 A - - - intergenic_variant - - - - - - rs7606063 2:78708111 A - - - intergenic_variant - - - - - - rs283827 2:79233364 T - - - intergenic_variant - - - - - - rs399603 2:79287965 G - - - intergenic_variant - - - - - - rs1376617 2:79623028 A - - - intergenic_variant - - - - - - rs978932 2:79921782 A 1496 NM_004389.3 Transcript intron_variant - - - - - - rs978932 2:79921782 A ENSESTG00000028828 ENSESTT00000072570 Transcript intron_variant - - - - - - rs978932 2:79921782 A ENSESTG00000028828 ENSESTT00000072553 Transcript intron_variant - - - - - - rs978932 2:79921782 A CCDS42703.2 CCDS42703.2 Transcript intron_variant - - - - - - rs978932 2:79921782 A 1496 NM_001164883.1 Transcript intron_variant - - - - - - rs978932 2:79921782 A CCDS54371.1 CCDS54371.1 Transcript intron_variant - - - - - - rs978932 2:79921782 A ENSESTG00000028828 ENSESTT00000072603 Transcript intron_variant - - - - - - rs978932 2:79921782 A ENSESTG00000028828 ENSESTT00000072631 Transcript intron_variant - - - - - - rs978932 2:79921782 A ENSESTG00000028828 ENSESTT00000072612 Transcript intron_variant - - - - - - rs7589515 2:80244685 A CCDS42703.2 CCDS42703.2 Transcript intron_variant - - - - - - rs7589515 2:80244685 A 1496 NM_004389.3 Transcript intron_variant - - - - - - rs7589515 2:80244685 A 1496 NM_001164883.1 Transcript intron_variant - - - - - - rs7589515 2:80244685 A CCDS54371.1 CCDS54371.1 Transcript intron_variant - - - - - - rs310779 2:80498520 G CCDS42703.2 CCDS42703.2 Transcript intron_variant - - - - - - rs310779 2:80498520 G 1496 NM_004389.3 Transcript intron_variant - - - - - - rs310779 2:80498520 G 1496 NM_001164883.1 Transcript intron_variant - - - - - - rs310779 2:80498520 G CCDS54371.1 CCDS54371.1 Transcript intron_variant - - - - - - rs310785 2:80544722 G ENSESTG00000028876 ENSESTT00000072717 Transcript intron_variant - - - - - - rs310785 2:80544722 G CCDS42703.2 CCDS42703.2 Transcript intron_variant - - - - - - rs310785 2:80544722 G 1496 NM_004389.3 Transcript intron_variant - - - - - - rs310785 2:80544722 G ENSESTG00000028876 ENSESTT00000072744 Transcript intron_variant - - - - - - rs310785 2:80544722 G 1496 NM_001164883.1 Transcript intron_variant - - - - - - rs310785 2:80544722 G CCDS54371.1 CCDS54371.1 Transcript intron_variant - - - - - - rs6709792 2:80613272 C ENSESTG00000028876 ENSESTT00000072717 Transcript intron_variant - - - - - - rs6709792 2:80613272 C CCDS42703.2 CCDS42703.2 Transcript intron_variant - - - - - - rs6709792 2:80613272 C 1496 NM_004389.3 Transcript intron_variant - - - - - - rs6709792 2:80613272 C ENSESTG00000028876 ENSESTT00000072744 Transcript intron_variant - - - - - - rs6709792 2:80613272 C 1496 NM_001164883.1 Transcript intron_variant - - - - - - rs6709792 2:80613272 C ENSESTG00000028876 ENSESTT00000072764 Transcript intron_variant - - - - - - rs6709792 2:80613272 C CCDS54371.1 CCDS54371.1 Transcript intron_variant - - - - - - rs920876 2:80628826 C ENSESTG00000028876 ENSESTT00000072717 Transcript intron_variant - - - - - - rs920876 2:80628826 C CCDS42703.2 CCDS42703.2 Transcript intron_variant - - - - - - rs920876 2:80628826 C 1496 NM_004389.3 Transcript intron_variant - - - - - - rs920876 2:80628826 C ENSESTG00000028876 ENSESTT00000072744 Transcript intron_variant - - - - - - rs920876 2:80628826 C 1496 NM_001164883.1 Transcript intron_variant - - - - - - rs920876 2:80628826 C ENSESTG00000028876 ENSESTT00000072764 Transcript intron_variant - - - - - - rs920876 2:80628826 C CCDS54371.1 CCDS54371.1 Transcript intron_variant - - - - - - rs10193274 2:83271035 G - - - intergenic_variant - - - - - - rs1246251 2:83326624 C - - - intergenic_variant - - - - - - rs1019836 2:83347135 T - - - intergenic_variant - - - - - - rs3099880 2:83972694 A - - - intergenic_variant - - - - - - rs4444541 2:84630814 G - - - intergenic_variant - - - - - - rs10203179 2:85100401 G CCDS46349.1 CCDS46349.1 Transcript intron_variant - - - - - - rs10203179 2:85100401 G 129293 NM_001080824.1 Transcript intron_variant - - - - - - rs10203179 2:85100401 G ENSESTG00000010282 ENSESTT00000025698 Transcript intron_variant - - - - - - rs10203179 2:85100401 G ENSESTG00000010282 ENSESTT00000025726 Transcript intron_variant - - - - - - rs10203179 2:85100401 G ENSESTG00000010282 ENSESTT00000025712 Transcript intron_variant - - - - - - rs4832125 2:85136995 C 9168 NM_021103.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3196 rs4832125 2:85136995 C ENSESTG00000010282 ENSESTT00000025698 Transcript upstream_gene_variant - - - - - - DISTANCE=2863 rs4832125 2:85136995 C ENSESTG00000010034 ENSESTT00000025092 Transcript downstream_gene_variant - - - - - - DISTANCE=3201 rs4832125 2:85136995 C CCDS1970.1 CCDS1970.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3448 rs6547605 2:85481312 A CCDS1971.1 CCDS1971.1 Transcript intron_variant - - - - - - rs6547605 2:85481312 A 83439 NM_031283.2 Transcript intron_variant - - - - - - rs6547605 2:85481312 A ENSESTG00000010062 ENSESTT00000025226 Transcript intron_variant - - - - - - rs6547605 2:85481312 A ENSESTG00000010062 ENSESTT00000025222 Transcript intron_variant - - - - - - rs4832038 2:86634688 G - - - intergenic_variant - - - - - - rs4971885 2:87108105 A ENSESTG00000033769 ENSESTT00000085374 Transcript upstream_gene_variant - - - - - - DISTANCE=2383 rs4971885 2:87108105 A 100286979 NR_037931.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2919868 2:88423374 C - ENSR00000676864 RegulatoryFeature regulatory_region_variant - - - - - - rs2919868 2:88423374 C CCDS2001.1 CCDS2001.1 Transcript intron_variant - - - - - - rs2919868 2:88423374 C ENSESTG00000027102 ENSESTT00000068381 Transcript intron_variant - - - - - - rs2919868 2:88423374 C 2168 NM_001443.2 Transcript intron_variant - - - - - - rs2919868 2:88423374 C ENSESTG00000027102 ENSESTT00000068336 Transcript intron_variant - - - - - - rs1878811 2:88493743 T - - - intergenic_variant - - - - - - rs2848121 2:89104073 A ENSESTG00000020066 ENSESTT00000050352 Transcript upstream_gene_variant - - - - - - DISTANCE=281 rs2848121 2:89104073 A ENSESTG00000020066 ENSESTT00000050325 Transcript intron_variant - - - - - - rs2848121 2:89104073 A ENSESTG00000020066 ENSESTT00000050314 Transcript intron_variant - - - - - - rs2848121 2:89104073 A 645784 NR_015424.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2848121 2:89104073 A ENSESTG00000020066 ENSESTT00000050341 Transcript upstream_gene_variant - - - - - - DISTANCE=155 rs2848121 2:89104073 A ENSESTG00000020066 ENSESTT00000050277 Transcript downstream_gene_variant - - - - - - DISTANCE=3240 rs842158 2:90242857 T - - - intergenic_variant - - - - - - rs10200128 2:96220041 T - - - intergenic_variant - - - - - - rs772158 2:97036196 G ENSESTG00000007806 ENSESTT00000019778 Transcript downstream_gene_variant - - - - - - DISTANCE=4399 rs772158 2:97036196 G CCDS2021.1 CCDS2021.1 Transcript intron_variant - - - - - - rs772158 2:97036196 G 23397 NM_015341.3 Transcript intron_variant - - - - - - rs772158 2:97036196 G ENSESTG00000007806 ENSESTT00000019767 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020648 Transcript intron_variant - - - - - - rs7593954 2:97265620 T 55683 NR_047658.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020695 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020715 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020645 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020603 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020692 Transcript intron_variant - - - - - - rs7593954 2:97265620 T 55683 NR_047657.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7593954 2:97265620 T 55683 NR_047655.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020658 Transcript intron_variant - - - - - - rs7593954 2:97265620 T CCDS46361.1 CCDS46361.1 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020739 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020733 Transcript downstream_gene_variant - - - - - - DISTANCE=562 rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020706 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020719 Transcript intron_variant - - - - - - rs7593954 2:97265620 T 55683 NR_047656.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020592 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020601 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020635 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020716 Transcript intron_variant - - - - - - rs7593954 2:97265620 T 55683 NR_047653.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020608 Transcript intron_variant - - - - - - rs7593954 2:97265620 T 55683 NR_047654.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020687 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020667 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020703 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020639 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020664 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020669 Transcript intron_variant - - - - - - rs7593954 2:97265620 T 55683 NM_001115016.2 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020730 Transcript intron_variant - - - - - - rs7593954 2:97265620 T ENSESTG00000008107 ENSESTT00000020700 Transcript intron_variant - - - - - - rs7608011 2:98322704 G ENSESTG00000013091 ENSESTT00000032844 Transcript downstream_gene_variant - - - - - - DISTANCE=3176 rs7608011 2:98322704 G ENSESTG00000013091 ENSESTT00000032842 Transcript downstream_gene_variant - - - - - - DISTANCE=3523 rs7608011 2:98322704 G ENSESTG00000013091 ENSESTT00000032833 Transcript downstream_gene_variant - - - - - - DISTANCE=3176 rs7608011 2:98322704 G 728537 NR_038386.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3175 rs7608011 2:98322704 G ENSESTG00000013091 ENSESTT00000032839 Transcript downstream_gene_variant - - - - - - DISTANCE=3176 rs6721250 2:98449796 T ENSESTG00000013139 ENSESTT00000032939 Transcript downstream_gene_variant - - - - - - DISTANCE=1304 rs6721250 2:98449796 T ENSESTG00000013139 ENSESTT00000032936 Transcript downstream_gene_variant - - - - - - DISTANCE=1304 rs6721250 2:98449796 T 23505 NM_015348.1 Transcript intron_variant - - - - - - rs6721250 2:98449796 T CCDS46368.1 CCDS46368.1 Transcript intron_variant - - - - - - rs2141863 2:98475482 G ENSESTG00000013139 ENSESTT00000032939 Transcript intron_variant - - - - - - rs2141863 2:98475482 G ENSESTG00000013139 ENSESTT00000032936 Transcript intron_variant - - - - - - rs2141863 2:98475482 G 23505 NM_015348.1 Transcript intron_variant - - - - - - rs2141863 2:98475482 G CCDS46368.1 CCDS46368.1 Transcript intron_variant - - - - - - rs2141863 2:98475482 G ENSESTG00000013139 ENSESTT00000032937 Transcript intron_variant - - - - - - rs6543240 2:98610924 T ENSESTG00000013139 ENSESTT00000032936 Transcript intron_variant - - - - - - rs6543240 2:98610924 T 23505 NM_015348.1 Transcript intron_variant - - - - - - rs6543240 2:98610924 T CCDS46368.1 CCDS46368.1 Transcript intron_variant - - - - - - rs6543240 2:98610924 T ENSESTG00000013139 ENSESTT00000032937 Transcript intron_variant - - - - - - rs1451250 2:98795523 C - ENSR00000594978 RegulatoryFeature regulatory_region_variant - - - - - - rs1451250 2:98795523 C CCDS42718.1 CCDS42718.1 Transcript intron_variant - - - - - - rs1451250 2:98795523 C 200403 NM_144992.4 Transcript intron_variant - - - - - - rs6736861 2:99028827 T - - - intergenic_variant - - - - - - rs7592884 2:99246522 A ENSESTG00000026655 ENSESTT00000067297 Transcript intron_variant - - - - - - rs7592884 2:99246522 A ENSESTG00000026655 ENSESTT00000067289 Transcript intron_variant - - - - - - rs7592884 2:99246522 A 11320 NM_001160154.1 Transcript intron_variant - - - - - - rs7592884 2:99246522 A CCDS2036.1 CCDS2036.1 Transcript intron_variant - - - - - - rs7592884 2:99246522 A ENSESTG00000026655 ENSESTT00000067333 Transcript intron_variant - - - - - - rs7592884 2:99246522 A CCDS54380.1 CCDS54380.1 Transcript intron_variant - - - - - - rs7592884 2:99246522 A 11320 NM_012214.2 Transcript intron_variant - - - - - - rs6733624 2:99726043 G ENSESTG00000030016 ENSESTT00000075637 Transcript intron_variant - - - - - - rs6733624 2:99726043 G ENSESTG00000030016 ENSESTT00000075652 Transcript intron_variant - - - - - - rs6733624 2:99726043 G ENSESTG00000030016 ENSESTT00000075600 Transcript intron_variant - - - - - - rs6733624 2:99726043 G 80705 NM_025244.2 Transcript intron_variant - - - - - - rs6733624 2:99726043 G ENSESTG00000030016 ENSESTT00000075535 Transcript intron_variant - - - - - - rs6733624 2:99726043 G 80705 NM_182911.3 Transcript intron_variant - - - - - - rs6733624 2:99726043 G CCDS2037.1 CCDS2037.1 Transcript upstream_gene_variant - - - - - - DISTANCE=141 rs6733624 2:99726043 G ENSESTG00000030016 ENSESTT00000075565 Transcript intron_variant - - - - - - rs6733624 2:99726043 G ENSESTG00000030016 ENSESTT00000075643 Transcript intron_variant - - - - - - rs4851223 2:100343557 T ENSESTG00000029646 ENSESTT00000074782 Transcript missense_variant 188 149 50 S/N aGt/aAt - rs4851223 2:100343557 T 3899 NM_001025108.1 Transcript missense_variant 1292 1148 383 S/N aGt/aAt - PolyPhen=benign;SIFT=tolerated rs4851223 2:100343557 T 3899 NM_002285.2 Transcript missense_variant 1309 1073 358 S/N aGt/aAt - PolyPhen=benign;SIFT=tolerated rs4851223 2:100343557 T CCDS33258.1 CCDS33258.1 Transcript missense_variant 1148 1148 383 S/N aGt/aAt - PolyPhen=benign;SIFT=tolerated rs4851223 2:100343557 T CCDS42723.1 CCDS42723.1 Transcript missense_variant 1073 1073 358 S/N aGt/aAt - PolyPhen=benign;SIFT=tolerated rs290780 2:102152860 T - - - intergenic_variant - - - - - - rs6543099 2:102475839 C - ENSR00001544885 RegulatoryFeature regulatory_region_variant - - - - - - rs6543099 2:102475839 C ENSESTG00000011233 ENSESTT00000028225 Transcript intron_variant - - - - - - rs6543099 2:102475839 C ENSESTG00000011233 ENSESTT00000028238 Transcript intron_variant - - - - - - rs6543099 2:102475839 C CCDS56130.1 CCDS56130.1 Transcript intron_variant - - - - - - rs6543099 2:102475839 C 9448 NM_001242559.1 Transcript intron_variant - - - - - - rs6543099 2:102475839 C ENSESTG00000011233 ENSESTT00000028246 Transcript intron_variant - - - - - - rs6543099 2:102475839 C ENSESTG00000011233 ENSESTT00000028258 Transcript intron_variant - - - - - - rs6543099 2:102475839 C ENSESTG00000011233 ENSESTT00000028269 Transcript upstream_gene_variant - - - - - - DISTANCE=265 rs6543099 2:102475839 C 9448 NM_001242560.1 Transcript intron_variant - - - - - - rs6543099 2:102475839 C ENSESTG00000011233 ENSESTT00000028261 Transcript intron_variant - - - - - - rs6543099 2:102475839 C 9448 NM_145687.3 Transcript intron_variant - - - - - - rs6543099 2:102475839 C ENSESTG00000011233 ENSESTT00000028263 Transcript intron_variant - - - - - - rs6543099 2:102475839 C 9448 NM_004834.4 Transcript intron_variant - - - - - - rs6543099 2:102475839 C 9448 NM_145686.3 Transcript intron_variant - - - - - - rs4375885 2:102655424 G - - - intergenic_variant - - - - - - rs10192220 2:102697497 A ENSESTG00000008998 ENSESTT00000022610 Transcript intron_variant - - - - - - rs10192220 2:102697497 A ENSESTG00000008998 ENSESTT00000022637 Transcript intron_variant - - - - - - rs10192220 2:102697497 A ENSESTG00000008998 ENSESTT00000022632 Transcript intron_variant - - - - - - rs10192220 2:102697497 A ENSESTG00000008998 ENSESTT00000022650 Transcript intron_variant - - - - - - rs10192220 2:102697497 A ENSESTG00000008998 ENSESTT00000022644 Transcript intron_variant - - - - - - rs10192220 2:102697497 A ENSESTG00000008998 ENSESTT00000022615 Transcript intron_variant - - - - - - rs10192220 2:102697497 A ENSESTG00000008998 ENSESTT00000022647 Transcript intron_variant - - - - - - rs10192220 2:102697497 A ENSESTG00000008998 ENSESTT00000022654 Transcript intron_variant - - - - - - rs1558651 2:103059613 G - ENSR00000677145 RegulatoryFeature regulatory_region_variant - - - - - - rs1558651 2:103059613 G ENSESTG00000009228 ENSESTT00000023125 Transcript intron_variant - - - - - - rs1558651 2:103059613 G CCDS2061.1 CCDS2061.1 Transcript intron_variant - - - - - - rs1558651 2:103059613 G 8807 NM_003853.2 Transcript intron_variant - - - - - - rs5006516 2:103214750 C - - - intergenic_variant - - - - - - rs6716746 2:104100014 G - - - intergenic_variant - - - - - - rs7592751 2:104653316 C ENSESTG00000006358 ENSESTT00000016045 Transcript intron_variant - - - - - - rs7592751 2:104653316 C ENSESTG00000006358 ENSESTT00000016047 Transcript intron_variant - - - - - - rs7592194 2:104689115 G ENSESTG00000006358 ENSESTT00000016045 Transcript downstream_gene_variant - - - - - - DISTANCE=362 rs1376613 2:105424871 G ENSESTG00000003999 ENSESTT00000010150 Transcript intron_variant - - - - - - rs1376613 2:105424871 G ENSESTG00000003999 ENSESTT00000010138 Transcript intron_variant - - - - - - rs1376613 2:105424871 G 100506421 NR_037883.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1376613 2:105424871 G ENSESTG00000003999 ENSESTT00000010133 Transcript intron_variant - - - - - - rs1376613 2:105424871 G ENSESTG00000003999 ENSESTT00000010140 Transcript intron_variant - - - - - - rs1376613 2:105424871 G ENSESTG00000003999 ENSESTT00000010159 Transcript intron_variant - - - - - - rs1376613 2:105424871 G ENSESTG00000004022 ENSESTT00000010162 Transcript intron_variant - - - - - - rs1376613 2:105424871 G ENSESTG00000003990 ENSESTT00000010091 Transcript intron_variant - - - - - - rs4581915 2:105736009 C - - - intergenic_variant - - - - - - rs2679835 2:105892856 G ENSESTG00000032441 ENSESTT00000081908 Transcript intron_variant - - - - - - rs2679835 2:105892856 G CCDS2067.1 CCDS2067.1 Transcript intron_variant - - - - - - rs2679835 2:105892856 G 9392 NM_004257.4 Transcript intron_variant - - - - - - rs2679835 2:105892856 G 9392 NM_001142621.1 Transcript intron_variant - - - - - - rs6543393 2:106826962 T - - - intergenic_variant - - - - - - rs6755065 2:107132819 A - - - intergenic_variant - - - - - - rs4283418 2:107137401 A ENSESTG00000007914 ENSESTT00000019951 Transcript downstream_gene_variant - - - - - - DISTANCE=958 rs4453690 2:107954034 C - ENSR00001545220 RegulatoryFeature regulatory_region_variant - - - - - - rs4453690 2:107954034 C - - - intergenic_variant - - - - - - rs831979 2:108385069 A - - - intergenic_variant - - - - - - rs1427340 2:108575280 C - - - intergenic_variant - - - - - - rs4676267 2:109864248 C 344558 NM_001099289.1 Transcript intron_variant - - - - - - rs6721096 2:110084915 C - ENSR00001545372 RegulatoryFeature regulatory_region_variant - - - - - - rs6721096 2:110084915 C 344558 NM_001099289.1 Transcript intron_variant - - - - - - rs58175962 2:112058065 G - - - intergenic_variant - - - - - - rs2878032 2:112073260 C - ENSR00000677314 RegulatoryFeature regulatory_region_variant - - - - - - rs2878032 2:112073260 C - - - intergenic_variant - - - - - - rs6542075 2:113451165 C - - - intergenic_variant - - - - - - rs6758463 2:113605400 A - - - intergenic_variant - - - - - - rs4449144 2:113703745 G - - - intergenic_variant - - - - - - rs6542106 2:113731717 A 56300 NM_019618.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3889 rs6542106 2:113731717 A CCDS2108.1 CCDS2108.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4499 rs6542106 2:113731717 A ENSESTG00000030044 ENSESTT00000075627 Transcript upstream_gene_variant - - - - - - DISTANCE=4496 rs4306724 2:115066932 T - - - intergenic_variant - - - - - - rs7589125 2:115108819 C - - - intergenic_variant - - - - - - rs6733788 2:115213331 C 57628 NM_020868.3 Transcript intron_variant - - - - - - rs6733788 2:115213331 C CCDS46400.1 CCDS46400.1 Transcript intron_variant - - - - - - rs4241131 2:115217398 T 57628 NM_020868.3 Transcript intron_variant - - - - - - rs4241131 2:115217398 T 57628 NM_001178036.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1782 rs4241131 2:115217398 T CCDS46400.1 CCDS46400.1 Transcript intron_variant - - - - - - rs2420047 2:115227521 T 57628 NM_020868.3 Transcript intron_variant - - - - - - rs2420047 2:115227521 T 57628 NM_001178036.1 Transcript intron_variant - - - - - - rs2420047 2:115227521 T CCDS46400.1 CCDS46400.1 Transcript intron_variant - - - - - - rs6542246 2:115884557 T 57628 NM_020868.3 Transcript intron_variant - - - - - - rs6542246 2:115884557 T 57628 NM_001178036.1 Transcript intron_variant - - - - - - rs6542246 2:115884557 T CCDS46400.1 CCDS46400.1 Transcript intron_variant - - - - - - rs6542246 2:115884557 T 57628 NM_001178037.1 Transcript intron_variant - - - - - - rs6542247 2:115899511 C 57628 NM_020868.3 Transcript intron_variant - - - - - - rs6542247 2:115899511 C 389023 NR_036580.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2114 rs6542247 2:115899511 C 57628 NM_001178036.1 Transcript intron_variant - - - - - - rs6542247 2:115899511 C ENSESTG00000002490 ENSESTT00000006170 Transcript downstream_gene_variant - - - - - - DISTANCE=2114 rs6542247 2:115899511 C CCDS46400.1 CCDS46400.1 Transcript intron_variant - - - - - - rs6542247 2:115899511 C 57628 NM_001178037.1 Transcript intron_variant - - - - - - rs1491541 2:117181737 A - - - intergenic_variant - - - - - - rs332903 2:117860070 C - - - intergenic_variant - - - - - - rs332926 2:117899084 G - - - intergenic_variant - - - - - - rs1377409 2:118003594 A - - - intergenic_variant - - - - - - rs333895 2:118011158 C - - - intergenic_variant - - - - - - rs334839 2:118122822 C - - - intergenic_variant - - - - - - rs6542428 2:118870643 G - ENSR00000597169 RegulatoryFeature regulatory_region_variant - - - - - - rs6542428 2:118870643 G CCDS2122.1 CCDS2122.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4745 rs6542428 2:118870643 G 51141 NM_016133.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3046 rs6723237 2:118885330 C - - - intergenic_variant - - - - - - rs1517534 2:119039362 C - - - intergenic_variant - - - - - - rs6542465 2:119235994 C - - - intergenic_variant - - - - - - rs4473383 2:119720051 G CCDS2124.1 CCDS2124.1 Transcript intron_variant - - - - - - rs4473383 2:119720051 G ENSESTG00000021863 ENSESTT00000055123 Transcript intron_variant - - - - - - rs4473383 2:119720051 G ENSESTG00000021863 ENSESTT00000055104 Transcript intron_variant - - - - - - rs4473383 2:119720051 G ENSESTG00000021863 ENSESTT00000055092 Transcript intron_variant - - - - - - rs4473383 2:119720051 G 8685 NM_006770.3 Transcript intron_variant - - - - - - rs708674 2:119992229 G - ENSR00000677461 RegulatoryFeature regulatory_region_variant - - - - - - rs708674 2:119992229 G CCDS42738.1 CCDS42738.1 Transcript intron_variant - - - - - - rs708674 2:119992229 G ENSESTG00000021981 ENSESTT00000055362 Transcript intron_variant - - - - - - rs708674 2:119992229 G 55240 NM_182915.2 Transcript intron_variant - - - - - - rs708674 2:119992229 G 55240 NM_001008410.1 Transcript intron_variant - - - - - - rs708674 2:119992229 G ENSESTG00000021981 ENSESTT00000055412 Transcript intron_variant - - - - - - rs708674 2:119992229 G 55240 NM_018234.2 Transcript intron_variant - - - - - - rs3111720 2:120631300 T 5775 NM_002830.3 Transcript intron_variant - - - - - - rs3111720 2:120631300 T CCDS2129.1 CCDS2129.1 Transcript intron_variant - - - - - - rs3111720 2:120631300 T ENSESTG00000022284 ENSESTT00000056253 Transcript intron_variant - - - - - - rs3111720 2:120631300 T ENSESTG00000022284 ENSESTT00000056287 Transcript intron_variant - - - - - - rs4353662 2:120657456 C ENSESTG00000020046 ENSESTT00000050386 Transcript upstream_gene_variant - - - - - - DISTANCE=873 rs4353662 2:120657456 C 5775 NM_002830.3 Transcript intron_variant - - - - - - rs4353662 2:120657456 C ENSESTG00000020046 ENSESTT00000050404 Transcript upstream_gene_variant - - - - - - DISTANCE=873 rs4353662 2:120657456 C CCDS2129.1 CCDS2129.1 Transcript intron_variant - - - - - - rs6748108 2:120719091 A 5775 NM_002830.3 Transcript intron_variant - - - - - - rs6748108 2:120719091 A ENSESTG00000020132 ENSESTT00000050471 Transcript intron_variant - - - - - - rs6748108 2:120719091 A ENSESTG00000020132 ENSESTT00000050521 Transcript upstream_gene_variant - - - - - - DISTANCE=1110 rs6748108 2:120719091 A ENSESTG00000020046 ENSESTT00000050427 Transcript downstream_gene_variant - - - - - - DISTANCE=4436 rs6748108 2:120719091 A ENSESTG00000020046 ENSESTT00000050386 Transcript downstream_gene_variant - - - - - - DISTANCE=4436 rs6748108 2:120719091 A ENSESTG00000020046 ENSESTT00000050404 Transcript downstream_gene_variant - - - - - - DISTANCE=4606 rs6748108 2:120719091 A CCDS2129.1 CCDS2129.1 Transcript intron_variant - - - - - - rs6748108 2:120719091 A ENSESTG00000020046 ENSESTT00000050431 Transcript downstream_gene_variant - - - - - - DISTANCE=4606 rs12711934 2:120733383 T 5775 NM_002830.3 Transcript intron_variant - - - - - - rs12711934 2:120733383 T ENSESTG00000020132 ENSESTT00000050471 Transcript intron_variant - - - - - - rs12711934 2:120733383 T CCDS2129.1 CCDS2129.1 Transcript intron_variant - - - - - - rs12711934 2:120733383 T ENSESTG00000020132 ENSESTT00000050521 Transcript intron_variant - - - - - - rs1665068 2:120870938 G 57669 NM_020909.3 Transcript intron_variant - - - - - - rs1665068 2:120870938 G ENSESTG00000020162 ENSESTT00000050738 Transcript intron_variant - - - - - - rs1665068 2:120870938 G CCDS54393.1 CCDS54393.1 Transcript intron_variant - - - - - - rs1665068 2:120870938 G 57669 NM_001184937.1 Transcript intron_variant - - - - - - rs1665068 2:120870938 G CCDS2130.1 CCDS2130.1 Transcript intron_variant - - - - - - rs2459787 2:120888894 A 57669 NM_020909.3 Transcript intron_variant - - - - - - rs2459787 2:120888894 A ENSESTG00000020162 ENSESTT00000050738 Transcript downstream_gene_variant - - - - - - DISTANCE=3230 rs2459787 2:120888894 A CCDS54393.1 CCDS54393.1 Transcript intron_variant - - - - - - rs2459787 2:120888894 A 57669 NM_001184937.1 Transcript intron_variant - - - - - - rs2459787 2:120888894 A ENSESTG00000020252 ENSESTT00000050830 Transcript upstream_gene_variant - - - - - - DISTANCE=330 rs2459787 2:120888894 A CCDS2130.1 CCDS2130.1 Transcript intron_variant - - - - - - rs7568413 2:121109612 C CCDS2132.1 CCDS2132.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2162 rs7568413 2:121109612 C 3625 NM_002193.2 Transcript downstream_gene_variant - - - - - - DISTANCE=229 rs7568413 2:121109612 C ENSESTG00000020371 ENSESTT00000051073 Transcript downstream_gene_variant - - - - - - DISTANCE=2440 rs6749784 2:121264551 G - - - intergenic_variant - - - - - - rs6541726 2:121339790 C - - - intergenic_variant - - - - - - rs4848629 2:121549800 C - ENSR00001546038 RegulatoryFeature regulatory_region_variant - - - - - - rs4848629 2:121549800 C ENSESTG00000020379 ENSESTT00000051104 Transcript intron_variant - - - - - - rs280214 2:121788733 T - - - intergenic_variant - - - - - - rs1158745 2:121886032 A - - - intergenic_variant - - - - - - rs7601735 2:121932734 T - ENSR00000597622 RegulatoryFeature regulatory_region_variant - - - - - - rs7601735 2:121932734 T ENSESTG00000014140 ENSESTT00000035340 Transcript upstream_gene_variant - - - - - - DISTANCE=3169 rs287800 2:122490152 A 84365 NM_032390.4 Transcript intron_variant - - - - - - rs287800 2:122490152 A 254128 NR_037857.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4016 rs287800 2:122490152 A ENSESTG00000014155 ENSESTT00000035446 Transcript upstream_gene_variant - - - - - - DISTANCE=4527 rs287800 2:122490152 A CCDS2135.1 CCDS2135.1 Transcript intron_variant - - - - - - rs287800 2:122490152 A ENSESTG00000014187 ENSESTT00000035517 Transcript intron_variant - - - - - - rs287800 2:122490152 A ENSESTG00000014187 ENSESTT00000035534 Transcript intron_variant - - - - - - rs287800 2:122490152 A ENSESTG00000014143 ENSESTT00000035368 Transcript downstream_gene_variant - - - - - - DISTANCE=4720 rs1517714 2:122717985 G - - - intergenic_variant - - - - - - rs294689 2:123548391 G - - - intergenic_variant - - - - - - rs1237219 2:124792066 C CCDS46401.1 CCDS46401.1 Transcript intron_variant - - - - - - rs1237219 2:124792066 C ENSESTG00000005079 ENSESTT00000012900 Transcript intron_variant - - - - - - rs1237219 2:124792066 C ENSESTG00000005079 ENSESTT00000012895 Transcript intron_variant - - - - - - rs1237219 2:124792066 C 129684 NM_130773.2 Transcript intron_variant - - - - - - rs1237219 2:124792066 C ENSESTG00000005079 ENSESTT00000012904 Transcript intron_variant - - - - - - rs2141540 2:124907716 A CCDS46401.1 CCDS46401.1 Transcript intron_variant - - - - - - rs2141540 2:124907716 A ENSESTG00000005079 ENSESTT00000012900 Transcript intron_variant - - - - - - rs2141540 2:124907716 A ENSESTG00000005079 ENSESTT00000012895 Transcript intron_variant - - - - - - rs2141540 2:124907716 A 129684 NM_130773.2 Transcript intron_variant - - - - - - rs1170588 2:125041494 G CCDS46401.1 CCDS46401.1 Transcript intron_variant - - - - - - rs1170588 2:125041494 G ENSESTG00000005079 ENSESTT00000012895 Transcript intron_variant - - - - - - rs1170588 2:125041494 G 129684 NM_130773.2 Transcript intron_variant - - - - - - rs1248544 2:125470284 T CCDS46401.1 CCDS46401.1 Transcript intron_variant - - - - - - rs1248544 2:125470284 T 129684 NM_130773.2 Transcript intron_variant - - - - - - rs2461310 2:125602775 C CCDS46401.1 CCDS46401.1 Transcript intron_variant - - - - - - rs2461310 2:125602775 C ENSESTG00000005086 ENSESTT00000012922 Transcript intron_variant - - - - - - rs2461310 2:125602775 C 129684 NM_130773.2 Transcript intron_variant - - - - - - rs2901408 2:125743086 C - - - intergenic_variant - - - - - - rs1229989 2:126261680 T - - - intergenic_variant - - - - - - rs4619616 2:126907424 C - - - intergenic_variant - - - - - - rs1595814 2:127346401 G - - - intergenic_variant - - - - - - rs6431189 2:127589366 C - ENSR00000597881 RegulatoryFeature regulatory_region_variant - - - - - - rs6431189 2:127589366 C - - - intergenic_variant - - - - - - rs7355336 2:128860835 G ENSESTG00000033900 ENSESTT00000085694 Transcript intron_variant - - - - - - rs7355336 2:128860835 G ENSESTG00000033900 ENSESTT00000085692 Transcript intron_variant - - - - - - rs7355336 2:128860835 G ENSESTG00000033900 ENSESTT00000085697 Transcript intron_variant - - - - - - rs7355336 2:128860835 G CCDS2154.1 CCDS2154.1 Transcript intron_variant - - - - - - rs7355336 2:128860835 G ENSESTG00000033900 ENSESTT00000085693 Transcript intron_variant - - - - - - rs7355336 2:128860835 G 56886 NR_027671.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs7355336 2:128860835 G 56886 NM_020120.3 Transcript intron_variant - - - - - - rs7564305 2:129094867 A - - - intergenic_variant - - - - - - rs4662819 2:129199645 A - - - intergenic_variant - - - - - - rs1251087 2:129268128 T - - - intergenic_variant - - - - - - rs893436 2:129775181 C - - - intergenic_variant - - - - - - rs7600460 2:129834637 G - - - intergenic_variant - - - - - - rs1251183 2:130074562 C - - - intergenic_variant - - - - - - rs6431089 2:130317890 G - - - intergenic_variant - - - - - - rs4662988 2:130477549 T - - - intergenic_variant - - - - - - rs62165319 2:131538917 G - - - intergenic_variant - - - - - - rs6430388 2:131633216 G ENSESTG00000022325 ENSESTT00000056342 Transcript intron_variant - - - - - - rs6430388 2:131633216 G ENSESTG00000022325 ENSESTT00000056354 Transcript intron_variant - - - - - - rs6430408 2:131656584 C ENSESTG00000022325 ENSESTT00000056342 Transcript intron_variant - - - - - - rs6430408 2:131656584 C ENSESTG00000022325 ENSESTT00000056354 Transcript intron_variant - - - - - - rs6752724 2:131672271 C ENSESTG00000022325 ENSESTT00000056342 Transcript downstream_gene_variant - - - - - - DISTANCE=213 rs6752724 2:131672271 C 50649 NM_015320.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1953 rs6752724 2:131672271 C 50649 NM_032995.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1953 rs6752724 2:131672271 C ENSESTG00000022325 ENSESTT00000056354 Transcript downstream_gene_variant - - - - - - DISTANCE=388 rs6752724 2:131672271 C ENSESTG00000022342 ENSESTT00000056383 Transcript upstream_gene_variant - - - - - - DISTANCE=2408 rs13015174 2:132259361 C ENSESTG00000022716 ENSESTT00000057452 Transcript downstream_gene_variant - - - - - - DISTANCE=1438 rs13015174 2:132259361 C ENSESTG00000022792 ENSESTT00000057511 Transcript upstream_gene_variant - - - - - - DISTANCE=4536 rs13015174 2:132259361 C 150776 NR_026922.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs13015174 2:132259361 C ENSESTG00000022716 ENSESTT00000057429 Transcript downstream_gene_variant - - - - - - DISTANCE=729 rs9712181 2:132543837 T - - - intergenic_variant - - - - - - rs6731424 2:133150901 T - - - intergenic_variant - - - - - - rs6718392 2:133150982 T - - - intergenic_variant - - - - - - rs4954350 2:133408845 C - ENSR00001546484 RegulatoryFeature regulatory_region_variant - - - - - - rs4954350 2:133408845 C 116372 NM_001077427.2 Transcript intron_variant - - - - - - rs4954350 2:133408845 C ENSESTG00000002373 ENSESTT00000005890 Transcript intron_variant - - - - - - rs4954350 2:133408845 C ENSESTG00000002373 ENSESTT00000005898 Transcript intron_variant - - - - - - rs4954350 2:133408845 C 116372 NM_144586.5 Transcript intron_variant - - - - - - rs4954350 2:133408845 C 2863 NM_001508.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4676 rs4954350 2:133408845 C CCDS42759.1 CCDS42759.1 Transcript intron_variant - - - - - - rs4954350 2:133408845 C CCDS46416.1 CCDS46416.1 Transcript intron_variant - - - - - - rs12691826 2:133485313 C ENSESTG00000002343 ENSESTT00000005858 Transcript downstream_gene_variant - - - - - - DISTANCE=4246 rs12691826 2:133485313 C CCDS46417.1 CCDS46417.1 Transcript intron_variant - - - - - - rs12691826 2:133485313 C 344148 NM_207481.3 Transcript intron_variant - - - - - - rs12691826 2:133485313 C ENSESTG00000002343 ENSESTT00000005866 Transcript downstream_gene_variant - - - - - - DISTANCE=4181 rs12691826 2:133485313 C 344148 NM_207363.2 Transcript intron_variant - - - - - - rs12691826 2:133485313 C CCDS46418.1 CCDS46418.1 Transcript intron_variant - - - - - - rs12691826 2:133485313 C ENSESTG00000002367 ENSESTT00000005875 Transcript intron_variant - - - - - - rs10207349 2:133580909 G ENSESTG00000002343 ENSESTT00000005858 Transcript intron_variant - - - - - - rs10207349 2:133580909 G CCDS46417.1 CCDS46417.1 Transcript intron_variant - - - - - - rs10207349 2:133580909 G 344148 NM_207481.3 Transcript intron_variant - - - - - - rs10207349 2:133580909 G 344148 NM_207363.2 Transcript intron_variant - - - - - - rs10207349 2:133580909 G CCDS46418.1 CCDS46418.1 Transcript intron_variant - - - - - - rs6748950 2:134265510 T CCDS46417.1 CCDS46417.1 Transcript intron_variant - - - - - - rs6748950 2:134265510 T 344148 NM_207481.3 Transcript intron_variant - - - - - - rs6748950 2:134265510 T 344148 NM_207363.2 Transcript intron_variant - - - - - - rs6748950 2:134265510 T CCDS46418.1 CCDS46418.1 Transcript intron_variant - - - - - - rs1901438 2:134437235 A - - - intergenic_variant - - - - - - rs6430459 2:134577344 C - - - intergenic_variant - - - - - - rs4245828 2:134718820 T - - - intergenic_variant - - - - - - rs2156002 2:135568095 G - - - intergenic_variant - - - - - - rs6430578 2:136280465 T ENSESTG00000014911 ENSESTT00000037326 Transcript intron_variant - - - - - - rs6430578 2:136280465 T 84083 NM_032143.2 Transcript intron_variant - - - - - - rs170115 2:136644332 C - - - intergenic_variant - - - - - - rs10187365 2:136953983 C - - - intergenic_variant - - - - - - rs841427 2:137308957 C - - - intergenic_variant - - - - - - rs2433921 2:137545011 T ENSESTG00000035261 ENSESTT00000089057 Transcript intron_variant - - - - - - rs1649549 2:137633935 T ENSESTG00000035261 ENSESTT00000089057 Transcript intron_variant - - - - - - rs7588779 2:137664470 A - ENSR00000304179 RegulatoryFeature regulatory_region_variant - - - - - - rs7588779 2:137664470 A ENSESTG00000035261 ENSESTT00000089057 Transcript intron_variant - - - - - - rs1202275 2:138060090 G 80731 NM_001080427.1 Transcript intron_variant - - - - - - rs6730384 2:138091707 T 80731 NM_001080427.1 Transcript intron_variant - - - - - - rs2044691 2:138350353 C 80731 NM_001080427.1 Transcript intron_variant - - - - - - rs1187137 2:138792523 T - - - intergenic_variant - - - - - - rs2375746 2:138839296 T - ENSR00001546749 RegulatoryFeature regulatory_region_variant - - - - - - rs2375746 2:138839296 T - - - intergenic_variant - - - - - - rs1547560 2:138880020 G - ENSR00001546759 RegulatoryFeature regulatory_region_variant - - - - - - rs1547560 2:138880020 G - - - intergenic_variant - - - - - - rs1521755 2:139419789 T - - - intergenic_variant - - - - - - rs4245865 2:139544973 G - ENSR00000599217 RegulatoryFeature regulatory_region_variant - - - - - - rs4245865 2:139544973 G - - - intergenic_variant - - - - - - rs7567569 2:139871929 G - - - intergenic_variant - - - - - - rs10210895 2:139878953 T - - - intergenic_variant - - - - - - rs4245844 2:139912380 A - - - intergenic_variant - - - - - - rs6430827 2:139946553 A - - - intergenic_variant - - - - - - rs7424478 2:140270623 A - - - intergenic_variant - - - - - - rs1097780 2:140362089 G - - - intergenic_variant - - - - - - rs1920528 2:140667374 T - - - intergenic_variant - - - - - - rs1405927 2:140799576 G - - - intergenic_variant - - - - - - rs1996718 2:142071271 G 53353 NM_018557.2 Transcript intron_variant - - - - - - rs1996718 2:142071271 G CCDS2182.1 CCDS2182.1 Transcript intron_variant - - - - - - rs2683871 2:142134092 T 53353 NM_018557.2 Transcript intron_variant - - - - - - rs2683871 2:142134092 T CCDS2182.1 CCDS2182.1 Transcript intron_variant - - - - - - rs4954904 2:142172348 A 53353 NM_018557.2 Transcript intron_variant - - - - - - rs4954904 2:142172348 A CCDS2182.1 CCDS2182.1 Transcript intron_variant - - - - - - rs4637042 2:142264226 A 53353 NM_018557.2 Transcript intron_variant - - - - - - rs4637042 2:142264226 A CCDS2182.1 CCDS2182.1 Transcript intron_variant - - - - - - rs10928135 2:142847976 C 53353 NM_018557.2 Transcript intron_variant - - - - - - rs10928135 2:142847976 C CCDS2182.1 CCDS2182.1 Transcript intron_variant - - - - - - rs1449484 2:142871236 A 53353 NM_018557.2 Transcript intron_variant - - - - - - rs1449484 2:142871236 A CCDS2182.1 CCDS2182.1 Transcript intron_variant - - - - - - rs1608497 2:142960141 T - - - intergenic_variant - - - - - - rs1732601 2:142983646 A - - - intergenic_variant - - - - - - rs1348760 2:143075476 A - - - intergenic_variant - - - - - - rs10201760 2:143093710 C - - - intergenic_variant - - - - - - rs7581493 2:143113375 T - - - intergenic_variant - - - - - - rs6429965 2:143210784 C - - - intergenic_variant - - - - - - rs2381352 2:143329951 C - - - intergenic_variant - - - - - - rs6731343 2:143569886 T - - - intergenic_variant - - - - - - rs1439874 2:143731482 A - ENSR00001546909 RegulatoryFeature regulatory_region_variant - - - - - - rs1439874 2:143731482 A 8942 NM_003937.2 Transcript intron_variant - - - - - - rs1439874 2:143731482 A ENSESTG00000033024 ENSESTT00000083462 Transcript intron_variant - - - - - - rs1439874 2:143731482 A ENSESTG00000032883 ENSESTT00000083175 Transcript intron_variant - - - - - - rs1439874 2:143731482 A ENSESTG00000032883 ENSESTT00000083158 Transcript intron_variant - - - - - - rs1439874 2:143731482 A ENSESTG00000032883 ENSESTT00000083137 Transcript intron_variant - - - - - - rs1439874 2:143731482 A ENSESTG00000032883 ENSESTT00000083192 Transcript intron_variant - - - - - - rs1439874 2:143731482 A 8942 NM_001032998.1 Transcript intron_variant - - - - - - rs1439874 2:143731482 A CCDS33299.1 CCDS33299.1 Transcript intron_variant - - - - - - rs1439874 2:143731482 A CCDS2183.1 CCDS2183.1 Transcript intron_variant - - - - - - rs1439874 2:143731482 A ENSESTG00000032883 ENSESTT00000083171 Transcript intron_variant - - - - - - rs1439874 2:143731482 A 8942 NM_001199241.1 Transcript intron_variant - - - - - - rs1439874 2:143731482 A ENSESTG00000032883 ENSESTT00000083185 Transcript intron_variant - - - - - - rs827211 2:143849346 G ENSESTG00000033024 ENSESTT00000083462 Transcript upstream_gene_variant - - - - - - DISTANCE=298 rs827211 2:143849346 G ENSESTG00000033018 ENSESTT00000083451 Transcript downstream_gene_variant - - - - - - DISTANCE=2878 rs189559 2:143920429 A CCDS2184.1 CCDS2184.1 Transcript intron_variant - - - - - - rs189559 2:143920429 A ENSESTG00000033022 ENSESTT00000083454 Transcript upstream_gene_variant - - - - - - DISTANCE=369 rs189559 2:143920429 A ENSESTG00000033018 ENSESTT00000083451 Transcript intron_variant - - - - - - rs189559 2:143920429 A ENSESTG00000032938 ENSESTT00000083274 Transcript intron_variant - - - - - - rs189559 2:143920429 A 55843 NM_018460.3 Transcript intron_variant - - - - - - rs354701 2:143935124 G - ENSR00000599460 RegulatoryFeature regulatory_region_variant - - - - - - rs354701 2:143935124 G CCDS2184.1 CCDS2184.1 Transcript intron_variant - - - - - - rs354701 2:143935124 G ENSESTG00000033018 ENSESTT00000083451 Transcript intron_variant - - - - - - rs354701 2:143935124 G ENSESTG00000032938 ENSESTT00000083274 Transcript intron_variant - - - - - - rs354701 2:143935124 G 55843 NM_018460.3 Transcript intron_variant - - - - - - rs7601537 2:144324272 C CCDS2184.1 CCDS2184.1 Transcript intron_variant - - - - - - rs7601537 2:144324272 C ENSESTG00000032938 ENSESTT00000083358 Transcript intron_variant - - - - - - rs7601537 2:144324272 C ENSESTG00000032938 ENSESTT00000083349 Transcript intron_variant - - - - - - rs7601537 2:144324272 C 55843 NM_018460.3 Transcript intron_variant - - - - - - rs7601537 2:144324272 C ENSESTG00000032938 ENSESTT00000083333 Transcript intron_variant - - - - - - rs10928191 2:144395086 A CCDS2184.1 CCDS2184.1 Transcript intron_variant - - - - - - rs10928191 2:144395086 A ENSESTG00000032990 ENSESTT00000083397 Transcript downstream_gene_variant - - - - - - DISTANCE=3251 rs10928191 2:144395086 A ENSESTG00000032938 ENSESTT00000083333 Transcript intron_variant - - - - - - rs10928191 2:144395086 A ENSESTG00000032938 ENSESTT00000083349 Transcript intron_variant - - - - - - rs10928191 2:144395086 A ENSESTG00000032938 ENSESTT00000083358 Transcript intron_variant - - - - - - rs10928191 2:144395086 A ENSESTG00000032938 ENSESTT00000083368 Transcript intron_variant - - - - - - rs10928191 2:144395086 A 55843 NM_018460.3 Transcript intron_variant - - - - - - rs10928191 2:144395086 A ENSESTG00000032990 ENSESTT00000083401 Transcript downstream_gene_variant - - - - - - DISTANCE=3244 rs9973909 2:144771466 C CCDS33300.1 CCDS33300.1 Transcript intron_variant - - - - - - rs9973909 2:144771466 C 79712 NM_001164629.2 Transcript intron_variant - - - - - - rs9973909 2:144771466 C ENSESTG00000024105 ENSESTT00000061003 Transcript intron_variant - - - - - - rs9973909 2:144771466 C ENSESTG00000024105 ENSESTT00000061026 Transcript intron_variant - - - - - - rs9973909 2:144771466 C 79712 NM_001006636.3 Transcript intron_variant - - - - - - rs9973909 2:144771466 C CCDS2185.1 CCDS2185.1 Transcript intron_variant - - - - - - rs9973909 2:144771466 C 79712 NM_024659.4 Transcript intron_variant - - - - - - rs890584 2:145212984 G ENSESTG00000024051 ENSESTT00000060797 Transcript intron_variant - - - - - - rs890584 2:145212984 G ENSESTG00000024051 ENSESTT00000060870 Transcript intron_variant - - - - - - rs890584 2:145212984 G CCDS2186.1 CCDS2186.1 Transcript intron_variant - - - - - - rs890584 2:145212984 G ENSESTG00000024051 ENSESTT00000060897 Transcript intron_variant - - - - - - rs890584 2:145212984 G ENSESTG00000024051 ENSESTT00000060831 Transcript intron_variant - - - - - - rs890584 2:145212984 G ENSESTG00000024051 ENSESTT00000060819 Transcript intron_variant - - - - - - rs890584 2:145212984 G 9839 NM_001171653.1 Transcript intron_variant - - - - - - rs890584 2:145212984 G ENSESTG00000024051 ENSESTT00000060876 Transcript intron_variant - - - - - - rs890584 2:145212984 G ENSESTG00000024051 ENSESTT00000060845 Transcript intron_variant - - - - - - rs890584 2:145212984 G CCDS54403.1 CCDS54403.1 Transcript intron_variant - - - - - - rs890584 2:145212984 G 9839 NM_014795.3 Transcript intron_variant - - - - - - rs890584 2:145212984 G ENSESTG00000024051 ENSESTT00000060850 Transcript intron_variant - - - - - - rs4662229 2:145471745 C 401014 NR_033870.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs4662229 2:145471745 C ENSESTG00000024032 ENSESTT00000060698 Transcript intron_variant - - - - - - rs4662229 2:145471745 C ENSESTG00000024032 ENSESTT00000060678 Transcript intron_variant - - - - - - rs1842979 2:145583243 A 401014 NR_033870.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs10204327 2:146032723 C - - - intergenic_variant - - - - - - rs6721246 2:146411628 A - - - intergenic_variant - - - - - - rs4427959 2:147193628 G - - - intergenic_variant - - - - - - rs6758308 2:147644269 G ENSESTG00000019129 ENSESTT00000048087 Transcript downstream_gene_variant - - - - - - DISTANCE=3423 rs1399683 2:147657782 A - - - intergenic_variant - - - - - - rs10179204 2:148148061 C - - - intergenic_variant - - - - - - rs1919446 2:148430673 G - - - intergenic_variant - - - - - - rs2382067 2:148435369 G - - - intergenic_variant - - - - - - rs2141457 2:148466290 T - - - intergenic_variant - - - - - - rs7559508 2:148494469 T - - - intergenic_variant - - - - - - rs4662547 2:148495200 G - - - intergenic_variant - - - - - - rs1227306 2:148701796 G 5000 NM_181741.3 Transcript intron_variant - - - - - - rs1227306 2:148701796 G 5000 NM_001190881.2 Transcript intron_variant - - - - - - rs1227306 2:148701796 G ENSESTG00000034128 ENSESTT00000086313 Transcript intron_variant - - - - - - rs1227306 2:148701796 G ENSESTG00000034128 ENSESTT00000086298 Transcript intron_variant - - - - - - rs1227306 2:148701796 G CCDS54404.1 CCDS54404.1 Transcript intron_variant - - - - - - rs1227306 2:148701796 G CCDS54405.1 CCDS54405.1 Transcript intron_variant - - - - - - rs1227306 2:148701796 G 5000 NM_181742.3 Transcript intron_variant - - - - - - rs1227306 2:148701796 G 5000 NM_001190882.2 Transcript intron_variant - - - - - - rs1227306 2:148701796 G 5000 NM_001190879.2 Transcript intron_variant - - - - - - rs1227306 2:148701796 G 5000 NM_002552.4 Transcript intron_variant - - - - - - rs1227306 2:148701796 G CCDS2187.1 CCDS2187.1 Transcript intron_variant - - - - - - rs1234407 2:148838760 T ENSESTG00000034076 ENSESTT00000086155 Transcript intron_variant - - - - - - rs1234407 2:148838760 T 55777 NM_018328.4 Transcript intron_variant - - - - - - rs1234407 2:148838760 T ENSESTG00000034076 ENSESTT00000086186 Transcript intron_variant - - - - - - rs1234407 2:148838760 T ENSESTG00000034076 ENSESTT00000086173 Transcript intron_variant - - - - - - rs1234407 2:148838760 T ENSESTG00000034076 ENSESTT00000086167 Transcript intron_variant - - - - - - rs1448896 2:149396554 A - - - intergenic_variant - - - - - - rs6430341 2:149557077 T - - - intergenic_variant - - - - - - rs848232 2:150513829 A ENSESTG00000024066 ENSESTT00000060835 Transcript intron_variant - - - - - - rs331105 2:150878734 C - - - intergenic_variant - - - - - - rs12692645 2:151096512 T - ENSR00000304431 RegulatoryFeature regulatory_region_variant - - - - - - rs12692645 2:151096512 T - - - intergenic_variant - - - - - - rs1441968 2:151164103 G - - - intergenic_variant - - - - - - rs12692736 2:151362396 G - - - intergenic_variant - - - - - - rs2341058 2:151473372 T ENSESTG00000029819 ENSESTT00000074990 Transcript intron_variant - - - - - - rs2341069 2:151487654 C - ENSR00001547471 RegulatoryFeature regulatory_region_variant - - - - - - rs2341069 2:151487654 C ENSESTG00000029791 ENSESTT00000074976 Transcript intron_variant - - - - - - rs2341069 2:151487654 C ENSESTG00000029791 ENSESTT00000074935 Transcript intron_variant - - - - - - rs12185605 2:151657456 T - - - intergenic_variant - - - - - - rs816706 2:151978260 A - - - intergenic_variant - - - - - - rs10197200 2:152685235 C - ENSR00000678016 RegulatoryFeature regulatory_region_variant - - - - - - rs10197200 2:152685235 C 26225 NM_001037174.1 Transcript upstream_gene_variant - - - - - - DISTANCE=226 rs10197200 2:152685235 C 785 NM_001005747.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4050 rs10197200 2:152685235 C ENSESTG00000019981 ENSESTT00000050149 Transcript upstream_gene_variant - - - - - - DISTANCE=524 rs10197200 2:152685235 C 26225 NM_177985.2 Transcript upstream_gene_variant - - - - - - DISTANCE=226 rs10197200 2:152685235 C CCDS2195.1 CCDS2195.1 Transcript upstream_gene_variant - - - - - - DISTANCE=545 rs10197200 2:152685235 C ENSESTG00000019981 ENSESTT00000050107 Transcript upstream_gene_variant - - - - - - DISTANCE=259 rs10197200 2:152685235 C 785 NM_000726.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4050 rs10197200 2:152685235 C 785 NM_001145798.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4050 rs10197200 2:152685235 C 785 NM_001005746.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4050 rs10197200 2:152685235 C 26225 NM_012097.3 Transcript upstream_gene_variant - - - - - - DISTANCE=226 rs2709763 2:152874715 T CCDS46426.1 CCDS46426.1 Transcript intron_variant - - - - - - rs2709763 2:152874715 T CCDS54409.1 CCDS54409.1 Transcript intron_variant - - - - - - rs2709763 2:152874715 T CCDS46427.1 CCDS46427.1 Transcript intron_variant - - - - - - rs2709763 2:152874715 T 785 NM_001145798.1 Transcript intron_variant - - - - - - rs2709763 2:152874715 T 785 NM_000726.3 Transcript intron_variant - - - - - - rs2709763 2:152874715 T 785 NM_001005746.2 Transcript intron_variant - - - - - - rs2345649 2:153045566 A - - - intergenic_variant - - - - - - rs4664546 2:153098958 G - - - intergenic_variant - - - - - - rs4644980 2:153150259 G ENSESTG00000019694 ENSESTT00000049363 Transcript upstream_gene_variant - - - - - - DISTANCE=2882 rs1960624 2:153768922 C - - - intergenic_variant - - - - - - rs1357644 2:153798791 C - - - intergenic_variant - - - - - - rs7574906 2:154014218 C - - - intergenic_variant - - - - - - rs10199738 2:154081245 T - - - intergenic_variant - - - - - - rs1221837 2:154244403 C - - - intergenic_variant - - - - - - rs1658552 2:154295719 C - - - intergenic_variant - - - - - - rs1940267 2:154428465 C - - - intergenic_variant - - - - - - rs2119721 2:154610622 C - - - intergenic_variant - - - - - - rs776878 2:154802352 G 114805 NM_052917.2 Transcript intron_variant - - - - - - rs776878 2:154802352 G CCDS2199.1 CCDS2199.1 Transcript intron_variant - - - - - - rs776878 2:154802352 G ENSESTG00000033411 ENSESTT00000084393 Transcript downstream_gene_variant - - - - - - DISTANCE=1291 rs3108892 2:154898825 G 114805 NM_052917.2 Transcript intron_variant - - - - - - rs3108892 2:154898825 G CCDS2199.1 CCDS2199.1 Transcript intron_variant - - - - - - rs2178567 2:154921488 C 114805 NM_052917.2 Transcript intron_variant - - - - - - rs2178567 2:154921488 C CCDS2199.1 CCDS2199.1 Transcript intron_variant - - - - - - rs3108893 2:154923189 C 114805 NM_052917.2 Transcript intron_variant - - - - - - rs3108893 2:154923189 C CCDS2199.1 CCDS2199.1 Transcript intron_variant - - - - - - rs4664725 2:155003245 A ENSESTG00000033420 ENSESTT00000084519 Transcript intron_variant - - - - - - rs4664725 2:155003245 A 114805 NM_052917.2 Transcript intron_variant - - - - - - rs4664725 2:155003245 A CCDS2199.1 CCDS2199.1 Transcript intron_variant - - - - - - rs1220608 2:155374399 G - - - intergenic_variant - - - - - - rs1220534 2:155426953 A - - - intergenic_variant - - - - - - rs1220528 2:155439026 G - - - intergenic_variant - - - - - - rs3106656 2:155570914 C ENSESTG00000023619 ENSESTT00000059565 Transcript intron_variant - - - - - - rs3106656 2:155570914 C 3760 NM_001260508.1 Transcript intron_variant - - - - - - rs3106656 2:155570914 C 3760 NM_001260509.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4552 rs3106656 2:155570914 C CCDS58733.1 CCDS58733.1 Transcript intron_variant - - - - - - rs3106656 2:155570914 C CCDS2200.1 CCDS2200.1 Transcript intron_variant - - - - - - rs3106656 2:155570914 C 3760 NM_002239.3 Transcript intron_variant - - - - - - rs2652439 2:155637987 A ENSESTG00000023619 ENSESTT00000059565 Transcript intron_variant - - - - - - rs2652439 2:155637987 A 3760 NM_001260508.1 Transcript intron_variant - - - - - - rs2652439 2:155637987 A CCDS58733.1 CCDS58733.1 Transcript intron_variant - - - - - - rs2652439 2:155637987 A CCDS2200.1 CCDS2200.1 Transcript intron_variant - - - - - - rs2652439 2:155637987 A 3760 NM_002239.3 Transcript intron_variant - - - - - - rs4349295 2:155808876 T - - - intergenic_variant - - - - - - rs2677467 2:156541362 C - - - intergenic_variant - - - - - - rs1283764 2:156549929 G - - - intergenic_variant - - - - - - rs1226415 2:157109702 C - - - intergenic_variant - - - - - - rs4664213 2:157588613 A ENSESTG00000001191 ENSESTT00000002827 Transcript intron_variant - - - - - - rs1383767 2:157904674 C - - - intergenic_variant - - - - - - rs895498 2:158161495 A - ENSR00001547751 RegulatoryFeature regulatory_region_variant - - - - - - rs895498 2:158161495 A 11227 NM_014568.1 Transcript intron_variant - - - - - - rs895498 2:158161495 A ENSESTG00000001133 ENSESTT00000002700 Transcript intron_variant - - - - - - rs895498 2:158161495 A CCDS2203.1 CCDS2203.1 Transcript intron_variant - - - - - - rs4606877 2:158366871 G - - - intergenic_variant - - - - - - rs7570512 2:159144661 G ENSESTG00000023552 ENSESTT00000059486 Transcript intron_variant - - - - - - rs7570512 2:159144661 G ENSESTG00000023552 ENSESTT00000059467 Transcript intron_variant - - - - - - rs7570512 2:159144661 G 130940 NM_138803.3 Transcript intron_variant - - - - - - rs7570512 2:159144661 G CCDS54410.1 CCDS54410.1 Transcript downstream_gene_variant - - - - - - DISTANCE=640 rs7570512 2:159144661 G 130940 NM_001171637.1 Transcript downstream_gene_variant - - - - - - DISTANCE=439 rs7570512 2:159144661 G CCDS33304.1 CCDS33304.1 Transcript intron_variant - - - - - - rs10194085 2:159180306 C ENSESTG00000023552 ENSESTT00000059486 Transcript intron_variant - - - - - - rs10194085 2:159180306 C ENSESTG00000023552 ENSESTT00000059467 Transcript intron_variant - - - - - - rs10194085 2:159180306 C 130940 NM_138803.3 Transcript intron_variant - - - - - - rs10194085 2:159180306 C CCDS54410.1 CCDS54410.1 Transcript intron_variant - - - - - - rs10194085 2:159180306 C 130940 NM_001171637.1 Transcript intron_variant - - - - - - rs10194085 2:159180306 C CCDS33304.1 CCDS33304.1 Transcript intron_variant - - - - - - rs4664251 2:159420831 T ENSESTG00000023414 ENSESTT00000059112 Transcript intron_variant - - - - - - rs4664251 2:159420831 T ENSESTG00000023414 ENSESTT00000059103 Transcript intron_variant - - - - - - rs4664251 2:159420831 T CCDS33306.1 CCDS33306.1 Transcript intron_variant - - - - - - rs4664251 2:159420831 T ENSESTG00000023414 ENSESTT00000059145 Transcript intron_variant - - - - - - rs4664251 2:159420831 T ENSESTG00000023414 ENSESTT00000059153 Transcript intron_variant - - - - - - rs4664251 2:159420831 T ENSESTG00000023414 ENSESTT00000059067 Transcript intron_variant - - - - - - rs4664251 2:159420831 T 8502 NM_001005476.1 Transcript intron_variant - - - - - - rs4664251 2:159420831 T CCDS33305.1 CCDS33305.1 Transcript intron_variant - - - - - - rs4664251 2:159420831 T 8502 NM_003628.3 Transcript intron_variant - - - - - - rs4664251 2:159420831 T ENSESTG00000023414 ENSESTT00000059155 Transcript intron_variant - - - - - - rs4664251 2:159420831 T ENSESTG00000023414 ENSESTT00000059093 Transcript intron_variant - - - - - - rs4664251 2:159420831 T ENSESTG00000023414 ENSESTT00000059137 Transcript intron_variant - - - - - - rs1554181 2:159685873 T ENSESTG00000023753 ENSESTT00000059941 Transcript intron_variant - - - - - - rs1554181 2:159685873 T ENSESTG00000023753 ENSESTT00000059894 Transcript intron_variant - - - - - - rs1608183 2:159768472 A - - - intergenic_variant - - - - - - rs6724810 2:160058730 C ENSESTG00000024166 ENSESTT00000061145 Transcript intron_variant - - - - - - rs6724810 2:160058730 C 85461 NM_033394.2 Transcript intron_variant - - - - - - rs6724810 2:160058730 C 85461 NM_001145909.1 Transcript intron_variant - - - - - - rs6724810 2:160058730 C CCDS42766.1 CCDS42766.1 Transcript intron_variant - - - - - - rs174264 2:160136337 A CCDS2208.1 CCDS2208.1 Transcript missense_variant 518 518 173 P/L cCg/cTg - PolyPhen=benign;SIFT=tolerated rs174264 2:160136337 A ENSESTG00000025001 ENSESTT00000063184 Transcript missense_variant 333 257 86 P/L cCg/cTg - rs174264 2:160136337 A 151525 NM_001128212.1 Transcript missense_variant 685 518 173 P/L cCg/cTg - PolyPhen=benign;SIFT=tolerated rs174264 2:160136337 A 151525 NM_001128213.1 Transcript missense_variant 775 518 173 P/L cCg/cTg - PolyPhen=benign;SIFT=tolerated rs174264 2:160136337 A 151525 NM_152528.2 Transcript missense_variant 667 518 173 P/L cCg/cTg - PolyPhen=benign;SIFT=tolerated rs174255 2:160154885 A - - - intergenic_variant - - - - - - rs1549384 2:160438795 A ENSESTG00000024352 ENSESTT00000061647 Transcript intron_variant - - - - - - rs1549384 2:160438795 A ENSESTG00000024352 ENSESTT00000061660 Transcript intron_variant - - - - - - rs1549384 2:160438795 A ENSESTG00000024352 ENSESTT00000061624 Transcript intron_variant - - - - - - rs1549384 2:160438795 A ENSESTG00000024352 ENSESTT00000061566 Transcript intron_variant - - - - - - rs1549384 2:160438795 A 29994 NM_013450.2 Transcript intron_variant - - - - - - rs2059700 2:160593317 T CCDS2210.1 CCDS2210.1 Transcript intron_variant - - - - - - rs2059700 2:160593317 T ENSESTG00000012994 ENSESTT00000032587 Transcript intron_variant - - - - - - rs2059700 2:160593317 T 64844 NM_022826.2 Transcript intron_variant - - - - - - rs7561426 2:160631648 T 9936 NM_014880.4 Transcript intron_variant - - - - - - rs7561426 2:160631648 T 9936 NM_001198763.1 Transcript intron_variant - - - - - - rs7561426 2:160631648 T CCDS33308.1 CCDS33308.1 Transcript intron_variant - - - - - - rs7561426 2:160631648 T CCDS56139.1 CCDS56139.1 Transcript intron_variant - - - - - - rs7561426 2:160631648 T CCDS56140.1 CCDS56140.1 Transcript intron_variant - - - - - - rs7561426 2:160631648 T 100526664 NM_001198760.1 Transcript intron_variant - - - - - - rs7561426 2:160631648 T CCDS56141.1 CCDS56141.1 Transcript intron_variant - - - - - - rs7561426 2:160631648 T 100526664 NM_001198759.1 Transcript intron_variant - - - - - - rs7561426 2:160631648 T ENSESTG00000013103 ENSESTT00000032856 Transcript intron_variant - - - - - - rs7561426 2:160631648 T 9936 NM_001198764.1 Transcript intron_variant - - - - - - rs2666994 2:160878850 C - ENSR00000678135 RegulatoryFeature regulatory_region_variant - - - - - - rs2666994 2:160878850 C 22925 NM_007366.4 Transcript intron_variant - - - - - - rs2666994 2:160878850 C 22925 NM_001007267.2 Transcript intron_variant - - - - - - rs2666994 2:160878850 C 22925 NM_001195641.1 Transcript intron_variant - - - - - - rs2666994 2:160878850 C CCDS42767.1 CCDS42767.1 Transcript intron_variant - - - - - - rs2666994 2:160878850 C CCDS33309.1 CCDS33309.1 Transcript intron_variant - - - - - - rs2666991 2:160882510 T 22925 NM_007366.4 Transcript intron_variant - - - - - - rs2666991 2:160882510 T 22925 NM_001007267.2 Transcript intron_variant - - - - - - rs2666991 2:160882510 T 22925 NM_001195641.1 Transcript intron_variant - - - - - - rs2666991 2:160882510 T CCDS42767.1 CCDS42767.1 Transcript intron_variant - - - - - - rs2666991 2:160882510 T CCDS33309.1 CCDS33309.1 Transcript intron_variant - - - - - - rs4413117 2:160932034 G - ENSR00000601097 RegulatoryFeature regulatory_region_variant - - - - - - rs4413117 2:160932034 G - - - intergenic_variant - - - - - - rs3111392 2:161106480 G ENSESTG00000013055 ENSESTT00000032745 Transcript intron_variant - - - - - - rs13006591 2:161142703 C - ENSR00000601144 RegulatoryFeature regulatory_region_variant - - - - - - rs13006591 2:161142703 C ENSESTG00000013017 ENSESTT00000032728 Transcript intron_variant - - - - - - rs13006591 2:161142703 C 5937 NM_016836.3 Transcript intron_variant - - - - - - rs13006591 2:161142703 C ENSESTG00000013017 ENSESTT00000032697 Transcript intron_variant - - - - - - rs13006591 2:161142703 C 5937 NM_002897.4 Transcript intron_variant - - - - - - rs13006591 2:161142703 C ENSESTG00000013017 ENSESTT00000032709 Transcript intron_variant - - - - - - rs13006591 2:161142703 C ENSESTG00000013017 ENSESTT00000032648 Transcript intron_variant - - - - - - rs13006591 2:161142703 C ENSESTG00000013017 ENSESTT00000032727 Transcript intron_variant - - - - - - rs13006591 2:161142703 C ENSESTG00000013017 ENSESTT00000032725 Transcript intron_variant - - - - - - rs13006591 2:161142703 C CCDS2213.1 CCDS2213.1 Transcript intron_variant - - - - - - rs13006591 2:161142703 C ENSESTG00000013017 ENSESTT00000032702 Transcript intron_variant - - - - - - rs270978 2:161694624 A - - - intergenic_variant - - - - - - rs270951 2:161727747 T - ENSR00001548066 RegulatoryFeature regulatory_region_variant - - - - - - rs270951 2:161727747 T - - - intergenic_variant - - - - - - rs1615606 2:161791166 C - ENSR00001548074 RegulatoryFeature regulatory_region_variant - - - - - - rs1615606 2:161791166 C - - - intergenic_variant - - - - - - rs4664388 2:161805096 T - - - intergenic_variant - - - - - - rs1710642 2:161810366 A - - - intergenic_variant - - - - - - rs7576911 2:161849686 T - - - intergenic_variant - - - - - - rs7591063 2:161849845 C - - - intergenic_variant - - - - - - rs7583564 2:161877954 C - - - intergenic_variant - - - - - - rs889917 2:162032836 C CCDS2215.1 CCDS2215.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3338 rs889917 2:162032836 C ENSESTG00000027275 ENSESTT00000068731 Transcript intron_variant - - - - - - rs889917 2:162032836 C ENSESTG00000027275 ENSESTT00000068751 Transcript intron_variant - - - - - - rs889917 2:162032836 C ENSESTG00000027275 ENSESTT00000068759 Transcript intron_variant - - - - - - rs889917 2:162032836 C 10010 NM_133484.1 Transcript intron_variant - - - - - - rs889917 2:162032836 C ENSESTG00000027275 ENSESTT00000068781 Transcript intron_variant - - - - - - rs889917 2:162032836 C 10010 NM_001199135.1 Transcript intron_variant - - - - - - rs889917 2:162032836 C 10010 NM_004180.2 Transcript intron_variant - - - - - - rs889917 2:162032836 C CCDS46436.1 CCDS46436.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3338 rs10190117 2:162153466 G - - - intergenic_variant - - - - - - rs1116165 2:162175290 C CCDS46437.1 CCDS46437.1 Transcript upstream_gene_variant - - - - - - DISTANCE=47 rs1116165 2:162175290 C 10213 NM_005805.5 Transcript intron_variant - - - - - - rs1116165 2:162175290 C ENSESTG00000027606 ENSESTT00000069827 Transcript intron_variant - - - - - - rs6432681 2:162267161 A CCDS46437.1 CCDS46437.1 Transcript intron_variant - - - - - - rs6432681 2:162267161 A 10213 NM_005805.5 Transcript intron_variant - - - - - - rs6432681 2:162267161 A ENSESTG00000027606 ENSESTT00000069827 Transcript intron_variant - - - - - - rs6432685 2:162309359 C - - - intergenic_variant - - - - - - rs1399649 2:162562026 T CCDS54412.1 CCDS54412.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3233 rs1399649 2:162562026 T 57282 NM_001178016.1 Transcript intron_variant - - - - - - rs1399649 2:162562026 T 57282 NM_001178015.1 Transcript intron_variant - - - - - - rs1399649 2:162562026 T CCDS46438.1 CCDS46438.1 Transcript intron_variant - - - - - - rs1399649 2:162562026 T ENSESTG00000029941 ENSESTT00000075480 Transcript intron_variant - - - - - - rs1399649 2:162562026 T ENSESTG00000029941 ENSESTT00000075544 Transcript intron_variant - - - - - - rs1399649 2:162562026 T CCDS54411.1 CCDS54411.1 Transcript intron_variant - - - - - - rs1399649 2:162562026 T ENSESTG00000029941 ENSESTT00000075506 Transcript intron_variant - - - - - - rs1399649 2:162562026 T 57282 NM_022058.3 Transcript intron_variant - - - - - - rs1399649 2:162562026 T ENSESTG00000029941 ENSESTT00000075564 Transcript intron_variant - - - - - - rs10196472 2:162954247 C ENSESTG00000030127 ENSESTT00000075809 Transcript downstream_gene_variant - - - - - - DISTANCE=2883 rs918160 2:163301297 G CCDS2220.1 CCDS2220.1 Transcript intron_variant - - - - - - rs918160 2:163301297 G 90134 NM_033272.3 Transcript intron_variant - - - - - - rs918160 2:163301297 G 90134 NM_173162.2 Transcript intron_variant - - - - - - rs918160 2:163301297 G CCDS2219.1 CCDS2219.1 Transcript intron_variant - - - - - - rs12464223 2:163462786 G CCDS2220.1 CCDS2220.1 Transcript intron_variant - - - - - - rs12464223 2:163462786 G 90134 NM_033272.3 Transcript intron_variant - - - - - - rs12464223 2:163462786 G 90134 NM_173162.2 Transcript intron_variant - - - - - - rs12464223 2:163462786 G CCDS2219.1 CCDS2219.1 Transcript intron_variant - - - - - - rs6705119 2:163523812 C CCDS2220.1 CCDS2220.1 Transcript intron_variant - - - - - - rs6705119 2:163523812 C 90134 NM_033272.3 Transcript intron_variant - - - - - - rs6705119 2:163523812 C 90134 NM_173162.2 Transcript intron_variant - - - - - - rs6705119 2:163523812 C CCDS2219.1 CCDS2219.1 Transcript intron_variant - - - - - - rs7606329 2:163921273 A - - - intergenic_variant - - - - - - rs4667943 2:163939531 T - - - intergenic_variant - - - - - - rs1235078 2:164230400 G - - - intergenic_variant - - - - - - rs2927198 2:164243695 A - - - intergenic_variant - - - - - - rs1221530 2:164246247 G - - - intergenic_variant - - - - - - rs1239136 2:164533445 T ENSESTG00000027554 ENSESTT00000069396 Transcript intron_variant - - - - - - rs1239136 2:164533445 T CCDS2221.2 CCDS2221.2 Transcript intron_variant - - - - - - rs1239136 2:164533445 T 55137 NM_018086.2 Transcript intron_variant - - - - - - rs1841406 2:164678556 T - - - intergenic_variant - - - - - - rs1437664 2:164785916 G - - - intergenic_variant - - - - - - rs2176239 2:164881274 G - - - intergenic_variant - - - - - - rs1446476 2:165010281 A - - - intergenic_variant - - - - - - rs6721995 2:165439663 C 2888 NM_004490.2 Transcript intron_variant - - - - - - rs6721995 2:165439663 C CCDS2222.1 CCDS2222.1 Transcript intron_variant - - - - - - rs355851 2:165626298 C ENSESTG00000028531 ENSESTT00000071840 Transcript intron_variant - - - - - - rs355851 2:165626298 C ENSESTG00000028531 ENSESTT00000071853 Transcript intron_variant - - - - - - rs355851 2:165626298 C ENSESTG00000028531 ENSESTT00000071828 Transcript intron_variant - - - - - - rs355851 2:165626298 C ENSESTG00000028531 ENSESTT00000071749 Transcript intron_variant - - - - - - rs355851 2:165626298 C ENSESTG00000028531 ENSESTT00000071874 Transcript intron_variant - - - - - - rs355851 2:165626298 C ENSESTG00000028531 ENSESTT00000071859 Transcript intron_variant - - - - - - rs355851 2:165626298 C 22837 NM_014900.3 Transcript intron_variant - - - - - - rs355851 2:165626298 C CCDS2223.2 CCDS2223.2 Transcript intron_variant - - - - - - rs10803793 2:165748972 C - - - intergenic_variant - - - - - - rs1439992 2:165968738 A 6328 NM_001081677.1 Transcript intron_variant - - - - - - rs1439992 2:165968738 A 6328 NM_006922.3 Transcript intron_variant - - - - - - rs1439992 2:165968738 A CCDS33312.1 CCDS33312.1 Transcript intron_variant - - - - - - rs1439992 2:165968738 A CCDS46440.1 CCDS46440.1 Transcript intron_variant - - - - - - rs1439992 2:165968738 A ENSESTG00000028462 ENSESTT00000071550 Transcript intron_variant - - - - - - rs1439992 2:165968738 A 6328 NM_001081676.1 Transcript intron_variant - - - - - - rs893774 2:166030536 G 6328 NM_001081677.1 Transcript intron_variant - - - - - - rs893774 2:166030536 G ENSESTG00000028446 ENSESTT00000071504 Transcript downstream_gene_variant - - - - - - DISTANCE=2244 rs893774 2:166030536 G ENSESTG00000028446 ENSESTT00000071490 Transcript intron_variant - - - - - - rs893774 2:166030536 G 6328 NM_006922.3 Transcript intron_variant - - - - - - rs893774 2:166030536 G CCDS33312.1 CCDS33312.1 Transcript intron_variant - - - - - - rs893774 2:166030536 G CCDS46440.1 CCDS46440.1 Transcript intron_variant - - - - - - rs893774 2:166030536 G 6328 NM_001081676.1 Transcript intron_variant - - - - - - rs965198 2:166483230 G CCDS2225.1 CCDS2225.1 Transcript intron_variant - - - - - - rs965198 2:166483230 G ENSESTG00000028399 ENSESTT00000071387 Transcript intron_variant - - - - - - rs965198 2:166483230 G ENSESTG00000028399 ENSESTT00000071453 Transcript intron_variant - - - - - - rs965198 2:166483230 G 80034 NM_001172173.1 Transcript intron_variant - - - - - - rs965198 2:166483230 G 80034 NM_024969.3 Transcript intron_variant - - - - - - rs7598251 2:166493997 C - ENSR00000601647 RegulatoryFeature regulatory_region_variant - - - - - - rs7598251 2:166493997 C CCDS2225.1 CCDS2225.1 Transcript intron_variant - - - - - - rs7598251 2:166493997 C ENSESTG00000028399 ENSESTT00000071387 Transcript intron_variant - - - - - - rs7598251 2:166493997 C ENSESTG00000028399 ENSESTT00000071453 Transcript intron_variant - - - - - - rs7598251 2:166493997 C 80034 NM_001172173.1 Transcript intron_variant - - - - - - rs7598251 2:166493997 C 80034 NM_024969.3 Transcript intron_variant - - - - - - rs1840252 2:166502611 G CCDS2225.1 CCDS2225.1 Transcript intron_variant - - - - - - rs1840252 2:166502611 G ENSESTG00000028399 ENSESTT00000071387 Transcript intron_variant - - - - - - rs1840252 2:166502611 G ENSESTG00000028399 ENSESTT00000071453 Transcript intron_variant - - - - - - rs1840252 2:166502611 G 80034 NM_001172173.1 Transcript intron_variant - - - - - - rs1840252 2:166502611 G 80034 NM_024969.3 Transcript intron_variant - - - - - - rs1559634 2:166574528 T - - - intergenic_variant - - - - - - rs10930216 2:167185307 A 6335 NM_002977.3 Transcript intron_variant - - - - - - rs10930216 2:167185307 A ENSESTG00000029932 ENSESTT00000075293 Transcript intron_variant - - - - - - rs4273234 2:167187321 G 6335 NM_002977.3 Transcript intron_variant - - - - - - rs4273234 2:167187321 G ENSESTG00000029932 ENSESTT00000075293 Transcript intron_variant - - - - - - rs10178216 2:167368715 A - - - intergenic_variant - - - - - - rs6743350 2:167407734 A - - - intergenic_variant - - - - - - rs6726002 2:167872077 C CCDS56143.1 CCDS56143.1 Transcript intron_variant - - - - - - rs6726002 2:167872077 C 129446 NM_152381.5 Transcript intron_variant - - - - - - rs6726002 2:167872077 C CCDS42768.1 CCDS42768.1 Transcript intron_variant - - - - - - rs6726002 2:167872077 C 129446 NM_001199143.1 Transcript intron_variant - - - - - - rs6726002 2:167872077 C CCDS42769.1 CCDS42769.1 Transcript intron_variant - - - - - - rs6726002 2:167872077 C 129446 NM_001079810.3 Transcript intron_variant - - - - - - rs7607013 2:167985693 T CCDS56143.1 CCDS56143.1 Transcript intron_variant - - - - - - rs7607013 2:167985693 T 129446 NM_152381.5 Transcript intron_variant - - - - - - rs7607013 2:167985693 T CCDS42768.1 CCDS42768.1 Transcript intron_variant - - - - - - rs7607013 2:167985693 T 129446 NM_001199143.1 Transcript intron_variant - - - - - - rs7607013 2:167985693 T CCDS42769.1 CCDS42769.1 Transcript intron_variant - - - - - - rs7607013 2:167985693 T 129446 NM_001079810.3 Transcript intron_variant - - - - - - rs7607013 2:167985693 T ENSESTG00000002720 ENSESTT00000006761 Transcript intron_variant - - - - - - rs4458185 2:168109117 A CCDS56143.1 CCDS56143.1 Transcript intron_variant - - - - - - rs4458185 2:168109117 A ENSESTG00000002699 ENSESTT00000006720 Transcript intron_variant - - - - - - rs4458185 2:168109117 A 129446 NM_001199145.1 Transcript intron_variant - - - - - - rs4458185 2:168109117 A CCDS56144.1 CCDS56144.1 Transcript intron_variant - - - - - - rs4458185 2:168109117 A CCDS42769.1 CCDS42769.1 Transcript intron_variant - - - - - - rs4458185 2:168109117 A 129446 NM_001199144.1 Transcript intron_variant - - - - - - rs4458185 2:168109117 A CCDS56145.1 CCDS56145.1 Transcript intron_variant - - - - - - rs4458185 2:168109117 A ENSESTG00000002711 ENSESTT00000006736 Transcript intron_variant - - - - - - rs4458185 2:168109117 A 129446 NM_152381.5 Transcript intron_variant - - - - - - rs4458185 2:168109117 A ENSESTG00000002694 ENSESTT00000006694 Transcript downstream_gene_variant - - - - - - DISTANCE=2769 rs4458185 2:168109117 A 129446 NM_001199143.1 Transcript intron_variant - - - - - - rs4458185 2:168109117 A CCDS42768.1 CCDS42768.1 Transcript intron_variant - - - - - - rs4458185 2:168109117 A ENSESTG00000002714 ENSESTT00000006746 Transcript upstream_gene_variant - - - - - - DISTANCE=4154 rs4458185 2:168109117 A 129446 NM_001079810.3 Transcript intron_variant - - - - - - rs7599361 2:168355241 T ENSESTG00000002705 ENSESTT00000006732 Transcript intron_variant - - - - - - rs1227134 2:168404634 G ENSESTG00000002705 ENSESTT00000006732 Transcript intron_variant - - - - - - rs1529308 2:168407837 C ENSESTG00000002705 ENSESTT00000006732 Transcript intron_variant - - - - - - rs1653399 2:168506275 A - - - intergenic_variant - - - - - - rs10460309 2:168788521 T - - - intergenic_variant - - - - - - rs12622064 2:169099800 G ENSESTG00000031639 ENSESTT00000079992 Transcript intron_variant - - - - - - rs12622064 2:169099800 G ENSESTG00000031639 ENSESTT00000079979 Transcript intron_variant - - - - - - rs12622064 2:169099800 G CCDS42770.1 CCDS42770.1 Transcript intron_variant - - - - - - rs12622064 2:169099800 G ENSESTG00000031639 ENSESTT00000079957 Transcript intron_variant - - - - - - rs12622064 2:169099800 G 27347 NM_013233.2 Transcript intron_variant - - - - - - rs4589714 2:169313753 T - ENSR00000601926 RegulatoryFeature regulatory_region_variant - - - - - - rs4589714 2:169313753 T ENSESTG00000031620 ENSESTT00000079789 Transcript intron_variant - - - - - - rs4589714 2:169313753 T CCDS58734.1 CCDS58734.1 Transcript intron_variant - - - - - - rs4589714 2:169313753 T CCDS2228.1 CCDS2228.1 Transcript intron_variant - - - - - - rs4589714 2:169313753 T 253782 NM_001256126.1 Transcript intron_variant - - - - - - rs4589714 2:169313753 T 253782 NM_203463.2 Transcript intron_variant - - - - - - rs4668069 2:169342130 G ENSESTG00000031620 ENSESTT00000079789 Transcript intron_variant - - - - - - rs4668069 2:169342130 G CCDS58734.1 CCDS58734.1 Transcript intron_variant - - - - - - rs4668069 2:169342130 G CCDS2228.1 CCDS2228.1 Transcript intron_variant - - - - - - rs4668069 2:169342130 G 253782 NM_001256126.1 Transcript intron_variant - - - - - - rs4668069 2:169342130 G 253782 NM_203463.2 Transcript intron_variant - - - - - - rs2892807 2:169829761 C 8647 NM_003742.2 Transcript intron_variant - - - - - - rs2892807 2:169829761 C CCDS46444.1 CCDS46444.1 Transcript intron_variant - - - - - - rs2892807 2:169829761 C ENSESTG00000015605 ENSESTT00000039077 Transcript upstream_gene_variant - - - - - - DISTANCE=4759 rs12477616 2:169845085 A 8647 NM_003742.2 Transcript intron_variant - - - - - - rs12477616 2:169845085 A CCDS46444.1 CCDS46444.1 Transcript intron_variant - - - - - - rs7592045 2:170047838 G 4036 NM_004525.2 Transcript intron_variant - - - - - - rs7592045 2:170047838 G ENSESTG00000015554 ENSESTT00000038953 Transcript intron_variant - - - - - - rs7592045 2:170047838 G CCDS2232.1 CCDS2232.1 Transcript intron_variant - - - - - - rs2544389 2:170124072 G 4036 NM_004525.2 Transcript intron_variant - - - - - - rs2544389 2:170124072 G ENSESTG00000015533 ENSESTT00000038903 Transcript intron_variant - - - - - - rs2544389 2:170124072 G CCDS2232.1 CCDS2232.1 Transcript intron_variant - - - - - - rs7561982 2:170333851 C CCDS2233.1 CCDS2233.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2213 rs7561982 2:170333851 C ENSESTG00000015391 ENSESTT00000038585 Transcript upstream_gene_variant - - - - - - DISTANCE=1837 rs7561982 2:170333851 C 129880 NM_152384.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2155 rs1381470 2:170954418 T - - - intergenic_variant - - - - - - rs4668213 2:171027576 C - - - intergenic_variant - - - - - - rs6712320 2:171431180 C 140469 NR_045684.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6712320 2:171431180 C CCDS42773.1 CCDS42773.1 Transcript intron_variant - - - - - - rs6712320 2:171431180 C CCDS46446.1 CCDS46446.1 Transcript intron_variant - - - - - - rs6712320 2:171431180 C 140469 NR_045683.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6712320 2:171431180 C 140469 NM_001083615.3 Transcript intron_variant - - - - - - rs6712320 2:171431180 C 140469 NR_045682.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6712320 2:171431180 C 140469 NM_138995.4 Transcript intron_variant - - - - - - rs1559965 2:171773781 G - ENSR00000678313 RegulatoryFeature regulatory_region_variant - - - - - - rs1559965 2:171773781 G - - - intergenic_variant - - - - - - rs2557804 2:171818289 A ENSESTG00000033323 ENSESTT00000084369 Transcript intron_variant - - - - - - rs2557804 2:171818289 A ENSESTG00000033323 ENSESTT00000084363 Transcript intron_variant - - - - - - rs2557804 2:171818289 A ENSESTG00000033323 ENSESTT00000084288 Transcript intron_variant - - - - - - rs2557804 2:171818289 A ENSESTG00000033323 ENSESTT00000084337 Transcript intron_variant - - - - - - rs2557804 2:171818289 A ENSESTG00000033323 ENSESTT00000084333 Transcript intron_variant - - - - - - rs2557804 2:171818289 A CCDS33325.1 CCDS33325.1 Transcript intron_variant - - - - - - rs2557804 2:171818289 A 26003 NM_001201428.1 Transcript intron_variant - - - - - - rs2557804 2:171818289 A ENSESTG00000033323 ENSESTT00000084293 Transcript intron_variant - - - - - - rs2557804 2:171818289 A ENSESTG00000033323 ENSESTT00000084358 Transcript intron_variant - - - - - - rs2557804 2:171818289 A 26003 NM_015530.4 Transcript intron_variant - - - - - - rs2557804 2:171818289 A ENSESTG00000033323 ENSESTT00000084349 Transcript intron_variant - - - - - - rs2162483 2:172038711 C 9874 NM_001136554.1 Transcript intron_variant - - - - - - rs7572973 2:172298155 T 80067 NM_001164821.1 Transcript intron_variant - - - - - - rs7572973 2:172298155 T ENSESTG00000033415 ENSESTT00000084427 Transcript intron_variant - - - - - - rs7572973 2:172298155 T ENSESTG00000033415 ENSESTT00000084423 Transcript intron_variant - - - - - - rs7572973 2:172298155 T 80067 NM_025000.3 Transcript intron_variant - - - - - - rs7572973 2:172298155 T ENSESTG00000033415 ENSESTT00000084426 Transcript intron_variant - - - - - - rs7572973 2:172298155 T ENSESTG00000033415 ENSESTT00000084428 Transcript intron_variant - - - - - - rs7572973 2:172298155 T 80067 NR_028482.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7572973 2:172298155 T CCDS54419.1 CCDS54419.1 Transcript intron_variant - - - - - - rs7572973 2:172298155 T CCDS2243.2 CCDS2243.2 Transcript intron_variant - - - - - - rs1185477 2:172319096 A 80067 NM_001164821.1 Transcript intron_variant - - - - - - rs1185477 2:172319096 A ENSESTG00000033415 ENSESTT00000084427 Transcript intron_variant - - - - - - rs1185477 2:172319096 A ENSESTG00000033415 ENSESTT00000084423 Transcript intron_variant - - - - - - rs1185477 2:172319096 A 80067 NM_025000.3 Transcript intron_variant - - - - - - rs1185477 2:172319096 A ENSESTG00000033415 ENSESTT00000084426 Transcript intron_variant - - - - - - rs1185477 2:172319096 A 80067 NR_028482.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1185477 2:172319096 A CCDS54419.1 CCDS54419.1 Transcript intron_variant - - - - - - rs1185477 2:172319096 A CCDS2243.2 CCDS2243.2 Transcript intron_variant - - - - - - rs10183083 2:172392460 T - ENSR00000305224 RegulatoryFeature regulatory_region_variant - - - - - - rs10183083 2:172392460 T CCDS46449.1 CCDS46449.1 Transcript intron_variant - - - - - - rs10183083 2:172392460 T 79901 NM_001127383.1 Transcript intron_variant - - - - - - rs10183083 2:172392460 T ENSESTG00000033434 ENSESTT00000084493 Transcript intron_variant - - - - - - rs10183083 2:172392460 T 79901 NM_024843.3 Transcript intron_variant - - - - - - rs10183083 2:172392460 T ENSESTG00000033434 ENSESTT00000084483 Transcript intron_variant - - - - - - rs10183083 2:172392460 T ENSESTG00000033434 ENSESTT00000084471 Transcript intron_variant - - - - - - rs10183083 2:172392460 T CCDS58736.1 CCDS58736.1 Transcript intron_variant - - - - - - rs10183083 2:172392460 T ENSESTG00000033434 ENSESTT00000084491 Transcript intron_variant - - - - - - rs10183083 2:172392460 T 79901 NM_001256909.1 Transcript intron_variant - - - - - - rs10183083 2:172392460 T CCDS2244.1 CCDS2244.1 Transcript intron_variant - - - - - - rs2542948 2:172418553 C 79901 NM_024843.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3910 rs2542948 2:172418553 C 79901 NM_001256909.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3910 rs2542948 2:172418553 C 79901 NM_001127383.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3910 rs6727050 2:172630399 T - - - intergenic_variant - - - - - - rs925880 2:172648623 C 8604 NR_047549.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs925880 2:172648623 C 8604 NM_003705.4 Transcript intron_variant - - - - - - rs925880 2:172648623 C CCDS33327.1 CCDS33327.1 Transcript intron_variant - - - - - - rs2138872 2:172696309 A ENSESTG00000022036 ENSESTT00000055603 Transcript downstream_gene_variant - - - - - - DISTANCE=4570 rs2138872 2:172696309 A 8604 NR_047549.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2138872 2:172696309 A 8604 NM_003705.4 Transcript intron_variant - - - - - - rs2138872 2:172696309 A CCDS33327.1 CCDS33327.1 Transcript intron_variant - - - - - - rs2138872 2:172696309 A ENSESTG00000022036 ENSESTT00000055656 Transcript intron_variant - - - - - - rs6737116 2:173085157 G - ENSR00000602364 RegulatoryFeature regulatory_region_variant - - - - - - rs6737116 2:173085157 G - - - intergenic_variant - - - - - - rs2357636 2:173335227 T 3655 NM_000210.2 Transcript intron_variant - - - - - - rs2357636 2:173335227 T 3655 NM_001079818.1 Transcript intron_variant - - - - - - rs2357636 2:173335227 T CCDS2249.1 CCDS2249.1 Transcript intron_variant - - - - - - rs2357636 2:173335227 T ENSESTG00000021467 ENSESTT00000053954 Transcript downstream_gene_variant - - - - - - DISTANCE=2965 rs2357636 2:173335227 T CCDS46451.1 CCDS46451.1 Transcript intron_variant - - - - - - rs2357636 2:173335227 T ENSESTG00000021467 ENSESTT00000053892 Transcript intron_variant - - - - - - rs2357636 2:173335227 T ENSESTG00000021467 ENSESTT00000053906 Transcript intron_variant - - - - - - rs7568186 2:173379297 C - ENSR00001548823 RegulatoryFeature regulatory_region_variant - - - - - - rs7568186 2:173379297 C - - - intergenic_variant - - - - - - rs10930580 2:174104837 C - ENSR00001548904 RegulatoryFeature regulatory_region_variant - - - - - - rs10930580 2:174104837 C ENSESTG00000017395 ENSESTT00000043771 Transcript intron_variant - - - - - - rs10930580 2:174104837 C ENSESTG00000017395 ENSESTT00000043780 Transcript intron_variant - - - - - - rs10930580 2:174104837 C CCDS42777.1 CCDS42777.1 Transcript intron_variant - - - - - - rs10930580 2:174104837 C 339751 NR_033882.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10930580 2:174104837 C 51776 NM_016653.2 Transcript intron_variant - - - - - - rs10930580 2:174104837 C ENSESTG00000017206 ENSESTT00000043438 Transcript intron_variant - - - - - - rs475269 2:174423537 G ENSESTG00000017352 ENSESTT00000043639 Transcript intron_variant - - - - - - rs475269 2:174423537 G ENSESTG00000017352 ENSESTT00000043630 Transcript intron_variant - - - - - - rs473389 2:174476402 T ENSESTG00000017352 ENSESTT00000043639 Transcript intron_variant - - - - - - rs473389 2:174476402 T ENSESTG00000017352 ENSESTT00000043630 Transcript intron_variant - - - - - - rs592208 2:174576227 A - - - intergenic_variant - - - - - - rs7591178 2:174903266 G - ENSR00001046338 RegulatoryFeature regulatory_region_variant - - - - - - rs7591178 2:174903266 G - - - intergenic_variant - - - - - - rs2646192 2:175580198 A 440926 NR_002315.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4330 rs2646171 2:175653643 A - ENSR00001044137 RegulatoryFeature regulatory_region_variant - - - - - - rs2646171 2:175653643 A ENSESTG00000031102 ENSESTT00000078295 Transcript upstream_gene_variant - - - - - - DISTANCE=987 rs2605297 2:175701133 G - ENSR00001549045 RegulatoryFeature regulatory_region_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078200 Transcript intron_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078135 Transcript intron_variant - - - - - - rs2605297 2:175701133 G 1123 NM_001822.5 Transcript intron_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078262 Transcript intron_variant - - - - - - rs2605297 2:175701133 G CCDS46454.1 CCDS46454.1 Transcript intron_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078230 Transcript intron_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078142 Transcript intron_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078222 Transcript downstream_gene_variant - - - - - - DISTANCE=710 rs2605297 2:175701133 G ENSESTG00000030839 ENSESTT00000077683 Transcript intron_variant - - - - - - rs2605297 2:175701133 G CCDS56147.1 CCDS56147.1 Transcript intron_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078171 Transcript intron_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078163 Transcript intron_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078251 Transcript intron_variant - - - - - - rs2605297 2:175701133 G CCDS46455.1 CCDS46455.1 Transcript intron_variant - - - - - - rs2605297 2:175701133 G 1123 NM_001025201.3 Transcript intron_variant - - - - - - rs2605297 2:175701133 G ENSESTG00000030937 ENSESTT00000078084 Transcript intron_variant - - - - - - rs2605297 2:175701133 G 1123 NM_001206602.1 Transcript intron_variant - - - - - - rs2605297 2:175701133 G 1123 NR_038133.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6433509 2:175783014 T ENSESTG00000030937 ENSESTT00000078200 Transcript intron_variant - - - - - - rs6433509 2:175783014 T CCDS46455.1 CCDS46455.1 Transcript intron_variant - - - - - - rs6433509 2:175783014 T 1123 NM_001025201.3 Transcript intron_variant - - - - - - rs6433509 2:175783014 T ENSESTG00000030937 ENSESTT00000078135 Transcript intron_variant - - - - - - rs6433509 2:175783014 T 1123 NM_001822.5 Transcript intron_variant - - - - - - rs6433509 2:175783014 T ENSESTG00000030937 ENSESTT00000078187 Transcript intron_variant - - - - - - rs6433509 2:175783014 T ENSESTG00000030937 ENSESTT00000078084 Transcript intron_variant - - - - - - rs6433509 2:175783014 T CCDS46454.1 CCDS46454.1 Transcript intron_variant - - - - - - rs6433509 2:175783014 T ENSESTG00000030937 ENSESTT00000078142 Transcript intron_variant - - - - - - rs6433509 2:175783014 T ENSESTG00000030839 ENSESTT00000077683 Transcript intron_variant - - - - - - rs6433509 2:175783014 T ENSESTG00000030937 ENSESTT00000078171 Transcript intron_variant - - - - - - rs6433509 2:175783014 T ENSESTG00000030937 ENSESTT00000078163 Transcript intron_variant - - - - - - rs6433509 2:175783014 T 1123 NR_038133.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2116987 2:176015158 A 1386 NM_001256094.1 Transcript intron_variant - - - - - - rs2116987 2:176015158 A 1386 NR_045774.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2116987 2:176015158 A 1386 NR_045770.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2116987 2:176015158 A 1386 NM_001256092.1 Transcript intron_variant - - - - - - rs2116987 2:176015158 A 1386 NR_045771.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2116987 2:176015158 A 1386 NR_045773.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2116987 2:176015158 A 1386 NR_045769.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2116987 2:176015158 A 1386 NR_045768.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2116987 2:176015158 A 1386 NM_001880.3 Transcript intron_variant - - - - - - rs2116987 2:176015158 A 1386 NR_045772.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2116987 2:176015158 A 1386 NM_001256090.1 Transcript intron_variant - - - - - - rs2116987 2:176015158 A 1386 NM_001256091.1 Transcript intron_variant - - - - - - rs2116987 2:176015158 A 1386 NM_001256093.1 Transcript intron_variant - - - - - - rs6728809 2:176204303 C ENSESTG00000030866 ENSESTT00000077747 Transcript intron_variant - - - - - - rs6728809 2:176204303 C ENSESTG00000030866 ENSESTT00000077740 Transcript intron_variant - - - - - - rs2461776 2:176297666 T ENSESTG00000030866 ENSESTT00000077747 Transcript intron_variant - - - - - - rs2461776 2:176297666 T ENSESTG00000030866 ENSESTT00000077740 Transcript intron_variant - - - - - - rs1554532 2:176404517 A - - - intergenic_variant - - - - - - rs2053740 2:176798287 T CCDS33332.1 CCDS33332.1 Transcript intron_variant - - - - - - rs2053740 2:176798287 T ENSESTG00000010201 ENSESTT00000025515 Transcript intron_variant - - - - - - rs2053740 2:176798287 T ENSESTG00000010201 ENSESTT00000025524 Transcript intron_variant - - - - - - rs2053740 2:176798287 T ENSESTG00000010201 ENSESTT00000025529 Transcript intron_variant - - - - - - rs2053740 2:176798287 T 80856 NM_030650.1 Transcript intron_variant - - - - - - rs2053740 2:176798287 T ENSESTG00000010201 ENSESTT00000025504 Transcript intron_variant - - - - - - rs2053740 2:176798287 T ENSESTG00000010201 ENSESTT00000025510 Transcript intron_variant - - - - - - rs2053740 2:176798287 T ENSESTG00000010201 ENSESTT00000025530 Transcript intron_variant - - - - - - rs847197 2:176956502 G ENSESTG00000010020 ENSESTT00000025069 Transcript upstream_gene_variant - - - - - - DISTANCE=1486 rs847197 2:176956502 G 3239 NM_000523.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1030 rs847197 2:176956502 G CCDS2264.2 CCDS2264.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1117 rs6433592 2:177332980 G - - - intergenic_variant - - - - - - rs1579938 2:177368588 T - - - intergenic_variant - - - - - - rs2969364 2:177482914 C - - - intergenic_variant - - - - - - rs1562607 2:177492223 C 375295 NR_040001.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2086 rs2122012 2:177493720 C 375295 NR_040001.1 Transcript downstream_gene_variant - - - - - - DISTANCE=589 rs963650 2:177495733 A 375295 NR_040001.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2969361 2:177497817 C 375295 NR_040001.1 Transcript non_coding_exon_variant,nc_transcript_variant 150 - - - - - rs2029040 2:177504650 G 375295 NR_040001.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2348 rs2710023 2:177515546 C - - - intergenic_variant - - - - - - rs2710019 2:177536575 C - - - intergenic_variant - - - - - - rs1527268 2:177770486 A - - - intergenic_variant - - - - - - rs1881702 2:177890564 A - - - intergenic_variant - - - - - - rs2364719 2:178102607 T CCDS46457.1 CCDS46457.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3611 rs2364719 2:178102607 T 4780 NM_001145413.2 Transcript intron_variant - - - - - - rs2364719 2:178102607 T ENSESTG00000032889 ENSESTT00000083130 Transcript intron_variant - - - - - - rs2364719 2:178102607 T 4780 NM_006164.4 Transcript intron_variant - - - - - - rs2364719 2:178102607 T CCDS46458.1 CCDS46458.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3611 rs2364719 2:178102607 T 4780 NM_001145412.2 Transcript intron_variant - - - - - - rs2364719 2:178102607 T CCDS42782.1 CCDS42782.1 Transcript intron_variant - - - - - - rs6743013 2:178320613 A CCDS2275.1 CCDS2275.1 Transcript intron_variant - - - - - - rs6743013 2:178320613 A ENSESTG00000032803 ENSESTT00000083044 Transcript intron_variant - - - - - - rs6743013 2:178320613 A ENSESTG00000032803 ENSESTT00000083066 Transcript intron_variant - - - - - - rs6743013 2:178320613 A ENSESTG00000032803 ENSESTT00000083037 Transcript intron_variant - - - - - - rs6743013 2:178320613 A ENSESTG00000032803 ENSESTT00000083061 Transcript intron_variant - - - - - - rs6743013 2:178320613 A 8540 NM_003659.3 Transcript intron_variant - - - - - - rs6743013 2:178320613 A ENSESTG00000032803 ENSESTT00000083027 Transcript intron_variant - - - - - - rs1992789 2:178358345 C CCDS2275.1 CCDS2275.1 Transcript intron_variant - - - - - - rs1992789 2:178358345 C ENSESTG00000032803 ENSESTT00000083044 Transcript downstream_gene_variant - - - - - - DISTANCE=416 rs1992789 2:178358345 C ENSESTG00000032803 ENSESTT00000083066 Transcript downstream_gene_variant - - - - - - DISTANCE=416 rs1992789 2:178358345 C ENSESTG00000032803 ENSESTT00000083037 Transcript intron_variant - - - - - - rs1992789 2:178358345 C ENSESTG00000032803 ENSESTT00000083061 Transcript intron_variant - - - - - - rs1992789 2:178358345 C 8540 NM_003659.3 Transcript intron_variant - - - - - - rs1992789 2:178358345 C ENSESTG00000032803 ENSESTT00000083027 Transcript intron_variant - - - - - - rs6433725 2:179264613 T 114880 NM_001201482.1 Transcript downstream_gene_variant - - - - - - DISTANCE=453 rs6433725 2:179264613 T ENSESTG00000030162 ENSESTT00000076271 Transcript downstream_gene_variant - - - - - - DISTANCE=3852 rs6433725 2:179264613 T 114880 NM_001201481.1 Transcript downstream_gene_variant - - - - - - DISTANCE=453 rs6433725 2:179264613 T 114880 NM_145739.2 Transcript downstream_gene_variant - - - - - - DISTANCE=453 rs6433725 2:179264613 T CCDS2277.1 CCDS2277.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4327 rs6433725 2:179264613 T 114880 NM_032523.3 Transcript downstream_gene_variant - - - - - - DISTANCE=453 rs6433725 2:179264613 T ENSESTG00000030162 ENSESTT00000076167 Transcript downstream_gene_variant - - - - - - DISTANCE=3852 rs6433725 2:179264613 T ENSESTG00000030162 ENSESTT00000076208 Transcript downstream_gene_variant - - - - - - DISTANCE=3852 rs6433725 2:179264613 T ENSESTG00000030162 ENSESTT00000076241 Transcript downstream_gene_variant - - - - - - DISTANCE=3852 rs6433725 2:179264613 T CCDS56152.1 CCDS56152.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4327 rs6433725 2:179264613 T CCDS2278.1 CCDS2278.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4327 rs6433725 2:179264613 T 114880 NM_001201480.1 Transcript downstream_gene_variant - - - - - - DISTANCE=453 rs6433725 2:179264613 T CCDS56151.1 CCDS56151.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4327 rs6433725 2:179264613 T ENSESTG00000030162 ENSESTT00000076322 Transcript downstream_gene_variant - - - - - - DISTANCE=3852 rs6433725 2:179264613 T CCDS56150.1 CCDS56150.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4327 rs6433725 2:179264613 T ENSESTG00000030349 ENSESTT00000076390 Transcript intron_variant - - - - - - rs7598830 2:179306016 G CCDS46460.1 CCDS46460.1 Transcript intron_variant - - - - - - rs7598830 2:179306016 G 8575 NM_001139517.1 Transcript intron_variant - - - - - - rs7598830 2:179306016 G 8575 NM_001139518.1 Transcript intron_variant - - - - - - rs7598830 2:179306016 G 8575 NM_003690.4 Transcript intron_variant - - - - - - rs7598830 2:179306016 G CCDS46461.1 CCDS46461.1 Transcript intron_variant - - - - - - rs7598830 2:179306016 G ENSESTG00000030661 ENSESTT00000077345 Transcript downstream_gene_variant - - - - - - DISTANCE=3170 rs7598830 2:179306016 G ENSESTG00000030661 ENSESTT00000077327 Transcript intron_variant - - - - - - rs7598830 2:179306016 G ENSESTG00000030661 ENSESTT00000077320 Transcript intron_variant - - - - - - rs7598830 2:179306016 G CCDS2279.1 CCDS2279.1 Transcript intron_variant - - - - - - rs7598830 2:179306016 G ENSESTG00000030661 ENSESTT00000077336 Transcript downstream_gene_variant - - - - - - DISTANCE=4206 rs7598830 2:179306016 G ENSESTG00000030661 ENSESTT00000077329 Transcript downstream_gene_variant - - - - - - DISTANCE=1933 rs7598830 2:179306016 G ENSESTG00000030661 ENSESTT00000077348 Transcript intron_variant - - - - - - rs7598830 2:179306016 G ENSESTG00000030661 ENSESTT00000077213 Transcript downstream_gene_variant - - - - - - DISTANCE=1933 rs7598830 2:179306016 G ENSESTG00000030349 ENSESTT00000076390 Transcript intron_variant - - - - - - rs1484117 2:179618790 A CCDS54421.1 CCDS54421.1 Transcript intron_variant - - - - - - rs1484117 2:179618790 A 7273 NM_001267550.1 Transcript intron_variant - - - - - - rs1484117 2:179618790 A CCDS54423.1 CCDS54423.1 Transcript intron_variant - - - - - - rs1484117 2:179618790 A 7273 NM_133432.3 Transcript intron_variant - - - - - - rs1484117 2:179618790 A 7273 NM_001256850.1 Transcript intron_variant - - - - - - rs1484117 2:179618790 A ENSESTG00000018993 ENSESTT00000047768 Transcript intron_variant - - - - - - rs1484117 2:179618790 A ENSESTG00000019296 ENSESTT00000048465 Transcript intron_variant - - - - - - rs1484117 2:179618790 A 7273 NM_003319.4 Transcript intron_variant - - - - - - rs1484117 2:179618790 A 7273 NM_133378.4 Transcript intron_variant - - - - - - rs1484117 2:179618790 A CCDS54422.1 CCDS54422.1 Transcript intron_variant - - - - - - rs1484117 2:179618790 A 7273 NM_133437.3 Transcript intron_variant - - - - - - rs1484117 2:179618790 A 7273 NM_133379.3 Transcript intron_variant - - - - - - rs1484117 2:179618790 A CCDS54424.1 CCDS54424.1 Transcript intron_variant - - - - - - rs1484117 2:179618790 A CCDS33337.1 CCDS33337.1 Transcript intron_variant - - - - - - rs12995981 2:179676511 A 7273 NM_001267550.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4361 rs12995981 2:179676511 A 7273 NM_133432.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4361 rs12995981 2:179676511 A 7273 NM_001256850.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4361 rs12995981 2:179676511 A ENSESTG00000019236 ENSESTT00000048362 Transcript upstream_gene_variant - - - - - - DISTANCE=4361 rs12995981 2:179676511 A 7273 NM_003319.4 Transcript upstream_gene_variant - - - - - - DISTANCE=4361 rs12995981 2:179676511 A 7273 NM_133378.4 Transcript upstream_gene_variant - - - - - - DISTANCE=4361 rs12995981 2:179676511 A 7273 NM_133437.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4361 rs12995981 2:179676511 A 7273 NM_133379.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4361 rs981921 2:179677637 C - - - intergenic_variant - - - - - - rs990493 2:179694102 C - ENSR00000603206 RegulatoryFeature regulatory_region_variant - - - - - - rs990493 2:179694102 C ENSESTG00000019231 ENSESTT00000048312 Transcript downstream_gene_variant - - - - - - DISTANCE=4705 rs990493 2:179694102 C 285025 NM_173648.3 Transcript downstream_gene_variant - - - - - - DISTANCE=382 rs6433739 2:179716742 T ENSESTG00000019194 ENSESTT00000048291 Transcript intron_variant - - - - - - rs6433739 2:179716742 T ENSESTG00000019194 ENSESTT00000048277 Transcript intron_variant - - - - - - rs6433739 2:179716742 T 285025 NM_173648.3 Transcript intron_variant - - - - - - rs6433740 2:179743129 G ENSESTG00000019184 ENSESTT00000048221 Transcript upstream_gene_variant - - - - - - DISTANCE=265 rs6433740 2:179743129 G 285025 NM_173648.3 Transcript intron_variant - - - - - - rs12693172 2:179756006 C - ENSR00000678462 RegulatoryFeature regulatory_region_variant - - - - - - rs12693172 2:179756006 C 285025 NM_173648.3 Transcript intron_variant - - - - - - rs1817803 2:180038397 A ENSESTG00000019071 ENSESTT00000048141 Transcript intron_variant - - - - - - rs1817803 2:180038397 A ENSESTG00000019071 ENSESTT00000048135 Transcript intron_variant - - - - - - rs1817803 2:180038397 A CCDS33338.1 CCDS33338.1 Transcript intron_variant - - - - - - rs1817803 2:180038397 A 91404 NM_178123.4 Transcript intron_variant - - - - - - rs1817803 2:180038397 A ENSESTG00000019071 ENSESTT00000047952 Transcript downstream_gene_variant - - - - - - DISTANCE=736 rs1817803 2:180038397 A ENSESTG00000019071 ENSESTT00000048151 Transcript intron_variant - - - - - - rs1817803 2:180038397 A ENSESTG00000019071 ENSESTT00000048156 Transcript intron_variant - - - - - - rs1817803 2:180038397 A ENSESTG00000019071 ENSESTT00000048174 Transcript intron_variant - - - - - - rs4894084 2:180090053 T 91404 NM_178123.4 Transcript intron_variant - - - - - - rs4894084 2:180090053 T ENSESTG00000019071 ENSESTT00000047952 Transcript intron_variant - - - - - - rs4894084 2:180090053 T ENSESTG00000019071 ENSESTT00000048141 Transcript intron_variant - - - - - - rs4894084 2:180090053 T ENSESTG00000019071 ENSESTT00000048156 Transcript intron_variant - - - - - - rs4894084 2:180090053 T ENSESTG00000019071 ENSESTT00000048151 Transcript intron_variant - - - - - - rs4894084 2:180090053 T ENSESTG00000019071 ENSESTT00000048135 Transcript intron_variant - - - - - - rs7422210 2:180225713 A - - - intergenic_variant - - - - - - rs6433792 2:180291589 C - - - intergenic_variant - - - - - - rs357713 2:180669917 T 151126 NM_152520.4 Transcript intron_variant - - - - - - rs1529118 2:181065399 T - - - intergenic_variant - - - - - - rs7589270 2:181401006 C - - - intergenic_variant - - - - - - rs7565823 2:182099017 C - - - intergenic_variant - - - - - - rs2099731 2:182188809 G - - - intergenic_variant - - - - - - rs265261 2:182219125 A - - - intergenic_variant - - - - - - rs265262 2:182220215 A - - - intergenic_variant - - - - - - rs265263 2:182220329 A - - - intergenic_variant - - - - - - rs166450 2:182226430 A ENSESTG00000029098 ENSESTT00000073253 Transcript upstream_gene_variant - - - - - - DISTANCE=1035 rs1993384 2:182406152 T CCDS42789.1 CCDS42789.1 Transcript intron_variant - - - - - - rs1993384 2:182406152 T CCDS33341.1 CCDS33341.1 Transcript intron_variant - - - - - - rs1993384 2:182406152 T CCDS33340.1 CCDS33340.1 Transcript intron_variant - - - - - - rs1993384 2:182406152 T 3676 NM_000885.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3678 rs1993384 2:182406152 T 375298 NM_001160277.1 Transcript intron_variant - - - - - - rs1993384 2:182406152 T 375298 NM_001030311.2 Transcript intron_variant - - - - - - rs1993384 2:182406152 T CCDS46466.1 CCDS46466.1 Transcript intron_variant - - - - - - rs1993384 2:182406152 T ENSESTG00000020870 ENSESTT00000052333 Transcript downstream_gene_variant - - - - - - DISTANCE=4870 rs1993384 2:182406152 T CCDS54425.1 CCDS54425.1 Transcript intron_variant - - - - - - rs1993384 2:182406152 T 375298 NR_027690.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1993384 2:182406152 T 375298 NM_201548.4 Transcript intron_variant - - - - - - rs1993384 2:182406152 T 375298 NM_001030313.2 Transcript intron_variant - - - - - - rs1993384 2:182406152 T 375298 NM_001030312.2 Transcript intron_variant - - - - - - rs1993384 2:182406152 T 375298 NR_027689.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs13031918 2:182623759 C - - - intergenic_variant - - - - - - rs6433932 2:182640421 A - ENSR00000305657 RegulatoryFeature regulatory_region_variant - - - - - - rs6433932 2:182640421 A - - - intergenic_variant - - - - - - rs1560373 2:183321033 T ENSESTG00000021297 ENSESTT00000053640 Transcript intron_variant - - - - - - rs1560373 2:183321033 T 5136 NM_005019.4 Transcript intron_variant - - - - - - rs1560373 2:183321033 T CCDS33344.1 CCDS33344.1 Transcript intron_variant - - - - - - rs1560373 2:183321033 T 5136 NM_001258312.1 Transcript intron_variant - - - - - - rs1560373 2:183321033 T CCDS2285.1 CCDS2285.1 Transcript intron_variant - - - - - - rs1560373 2:183321033 T 5136 NM_001003683.2 Transcript intron_variant - - - - - - rs1560373 2:183321033 T ENSESTG00000021297 ENSESTT00000053633 Transcript intron_variant - - - - - - rs825661 2:183537895 G - ENSR00000603624 RegulatoryFeature regulatory_region_variant - - - - - - rs825661 2:183537895 G - - - intergenic_variant - - - - - - rs288261 2:183573730 G - - - intergenic_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051554 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051771 Transcript upstream_gene_variant - - - - - - DISTANCE=3120 rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051744 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051756 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051572 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051542 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051767 Transcript upstream_gene_variant - - - - - - DISTANCE=3120 rs3098359 2:183616592 T CCDS33345.1 CCDS33345.1 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051738 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051558 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051704 Transcript intron_variant - - - - - - rs3098359 2:183616592 T 54431 NM_018981.1 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051689 Transcript intron_variant - - - - - - rs3098359 2:183616592 T ENSESTG00000020427 ENSESTT00000051722 Transcript intron_variant - - - - - - rs12476227 2:183876928 C CCDS2287.1 CCDS2287.1 Transcript intron_variant - - - - - - rs12476227 2:183876928 C 10787 NM_013436.3 Transcript intron_variant - - - - - - rs12476227 2:183876928 C ENSESTG00000021080 ENSESTT00000052998 Transcript intron_variant - - - - - - rs12476227 2:183876928 C CCDS2288.1 CCDS2288.1 Transcript intron_variant - - - - - - rs12476227 2:183876928 C 10787 NM_205842.1 Transcript intron_variant - - - - - - rs597456 2:184236367 A - - - intergenic_variant - - - - - - rs1919269 2:184434315 C - - - intergenic_variant - - - - - - rs10221575 2:184503889 C - - - intergenic_variant - - - - - - rs10171195 2:184818424 C ENSESTG00000002437 ENSESTT00000006032 Transcript downstream_gene_variant - - - - - - DISTANCE=4585 rs6434058 2:184918867 C - - - intergenic_variant - - - - - - rs6434069 2:185011679 G - - - intergenic_variant - - - - - - rs6434117 2:186114220 C - - - intergenic_variant - - - - - - rs1031295 2:187520774 G CCDS2292.1 CCDS2292.1 Transcript intron_variant - - - - - - rs1031295 2:187520774 G 3685 NM_001144999.1 Transcript intron_variant - - - - - - rs1031295 2:187520774 G 3685 NM_002210.3 Transcript intron_variant - - - - - - rs1031295 2:187520774 G ENSESTG00000029591 ENSESTT00000074826 Transcript intron_variant - - - - - - rs1031295 2:187520774 G CCDS46471.1 CCDS46471.1 Transcript intron_variant - - - - - - rs1031295 2:187520774 G CCDS46470.1 CCDS46470.1 Transcript intron_variant - - - - - - rs1031295 2:187520774 G 3685 NM_001145000.1 Transcript intron_variant - - - - - - rs1031295 2:187520774 G ENSESTG00000029591 ENSESTT00000074802 Transcript intron_variant - - - - - - rs1031295 2:187520774 G ENSESTG00000029591 ENSESTT00000074836 Transcript intron_variant - - - - - - rs1031295 2:187520774 G ENSESTG00000029591 ENSESTT00000074778 Transcript intron_variant - - - - - - rs6728186 2:187902906 A - - - intergenic_variant - - - - - - rs12693463 2:188010356 A - - - intergenic_variant - - - - - - rs6434205 2:188017129 T - - - intergenic_variant - - - - - - rs4277486 2:188025323 C - - - intergenic_variant - - - - - - rs4667148 2:188026833 A - - - intergenic_variant - - - - - - rs4480957 2:188033931 G - ENSR00000603910 RegulatoryFeature regulatory_region_variant - - - - - - rs4480957 2:188033931 G - - - intergenic_variant - - - - - - rs4496295 2:188035498 T - - - intergenic_variant - - - - - - rs4264537 2:188040938 C - - - intergenic_variant - - - - - - rs1528228 2:188119684 G - - - intergenic_variant - - - - - - rs11904497 2:188122304 G - - - intergenic_variant - - - - - - rs698589 2:188214870 A 10203 NM_005795.4 Transcript intron_variant - - - - - - rs698589 2:188214870 A CCDS2293.1 CCDS2293.1 Transcript intron_variant - - - - - - rs1011988 2:188222678 A 10203 NM_005795.4 Transcript intron_variant - - - - - - rs1011988 2:188222678 A CCDS2293.1 CCDS2293.1 Transcript intron_variant - - - - - - rs858757 2:188233906 C 10203 NM_005795.4 Transcript intron_variant - - - - - - rs858757 2:188233906 C CCDS2293.1 CCDS2293.1 Transcript intron_variant - - - - - - rs698577 2:188250301 A ENSESTG00000029924 ENSESTT00000075476 Transcript missense_variant 528 55 19 N/Y Aat/Tat - rs698577 2:188250301 A ENSESTG00000029924 ENSESTT00000075427 Transcript downstream_gene_variant - - - - - - DISTANCE=16 rs698577 2:188250301 A 10203 NM_005795.4 Transcript missense_variant 570 22 8 N/Y Aat/Tat - PolyPhen=benign;SIFT=tolerated rs698577 2:188250301 A ENSESTG00000029924 ENSESTT00000075342 Transcript missense_variant 395 55 19 N/Y Aat/Tat - rs698577 2:188250301 A CCDS2293.1 CCDS2293.1 Transcript missense_variant 22 22 8 N/Y Aat/Tat - PolyPhen=benign;SIFT=tolerated rs698577 2:188250301 A ENSESTG00000029924 ENSESTT00000075441 Transcript downstream_gene_variant - - - - - - DISTANCE=1825 rs698577 2:188250301 A ENSESTG00000029924 ENSESTT00000075518 Transcript downstream_gene_variant - - - - - - DISTANCE=1764 rs858760 2:188265305 T ENSESTG00000029924 ENSESTT00000075476 Transcript intron_variant - - - - - - rs858760 2:188265305 T ENSESTG00000029924 ENSESTT00000075427 Transcript intron_variant - - - - - - rs858760 2:188265305 T 10203 NM_005795.4 Transcript intron_variant - - - - - - rs858760 2:188265305 T ENSESTG00000029924 ENSESTT00000075342 Transcript intron_variant - - - - - - rs858760 2:188265305 T ENSESTG00000029924 ENSESTT00000075441 Transcript intron_variant - - - - - - rs858760 2:188265305 T ENSESTG00000029924 ENSESTT00000075518 Transcript intron_variant - - - - - - rs858761 2:188265621 G ENSESTG00000029924 ENSESTT00000075476 Transcript intron_variant - - - - - - rs858761 2:188265621 G ENSESTG00000029924 ENSESTT00000075427 Transcript intron_variant - - - - - - rs858761 2:188265621 G 10203 NM_005795.4 Transcript intron_variant - - - - - - rs858761 2:188265621 G ENSESTG00000029924 ENSESTT00000075342 Transcript intron_variant - - - - - - rs858761 2:188265621 G ENSESTG00000029924 ENSESTT00000075441 Transcript intron_variant - - - - - - rs858761 2:188265621 G ENSESTG00000029924 ENSESTT00000075518 Transcript intron_variant - - - - - - rs2048486 2:188279448 G ENSESTG00000029924 ENSESTT00000075476 Transcript intron_variant - - - - - - rs2048486 2:188279448 G ENSESTG00000029924 ENSESTT00000075427 Transcript intron_variant - - - - - - rs2048486 2:188279448 G 10203 NM_005795.4 Transcript intron_variant - - - - - - rs2048486 2:188279448 G ENSESTG00000029924 ENSESTT00000075342 Transcript intron_variant - - - - - - rs2048486 2:188279448 G ENSESTG00000029924 ENSESTT00000075441 Transcript intron_variant - - - - - - rs2048486 2:188279448 G ENSESTG00000029924 ENSESTT00000075518 Transcript intron_variant - - - - - - rs1511880 2:188290782 G ENSESTG00000029924 ENSESTT00000075476 Transcript intron_variant - - - - - - rs1511880 2:188290782 G ENSESTG00000029924 ENSESTT00000075427 Transcript intron_variant - - - - - - rs1511880 2:188290782 G 10203 NM_005795.4 Transcript intron_variant - - - - - - rs1511880 2:188290782 G ENSESTG00000029888 ENSESTT00000075148 Transcript downstream_gene_variant - - - - - - DISTANCE=4043 rs1511880 2:188290782 G ENSESTG00000029924 ENSESTT00000075342 Transcript intron_variant - - - - - - rs1511880 2:188290782 G ENSESTG00000029924 ENSESTT00000075441 Transcript intron_variant - - - - - - rs1511880 2:188290782 G ENSESTG00000029924 ENSESTT00000075518 Transcript intron_variant - - - - - - rs4666727 2:188299406 G - ENSR00000305763 RegulatoryFeature regulatory_region_variant - - - - - - rs4666727 2:188299406 G ENSESTG00000029924 ENSESTT00000075476 Transcript intron_variant - - - - - - rs4666727 2:188299406 G ENSESTG00000029924 ENSESTT00000075427 Transcript intron_variant - - - - - - rs4666727 2:188299406 G 10203 NM_005795.4 Transcript intron_variant - - - - - - rs4666727 2:188299406 G ENSESTG00000029924 ENSESTT00000075342 Transcript intron_variant - - - - - - rs4666727 2:188299406 G ENSESTG00000029924 ENSESTT00000075441 Transcript intron_variant - - - - - - rs4666727 2:188299406 G ENSESTG00000029924 ENSESTT00000075518 Transcript intron_variant - - - - - - rs12693469 2:188301732 A ENSESTG00000029924 ENSESTT00000075476 Transcript intron_variant - - - - - - rs12693469 2:188301732 A ENSESTG00000029924 ENSESTT00000075427 Transcript intron_variant - - - - - - rs12693469 2:188301732 A 10203 NM_005795.4 Transcript intron_variant - - - - - - rs12693469 2:188301732 A ENSESTG00000029924 ENSESTT00000075342 Transcript intron_variant - - - - - - rs12693469 2:188301732 A ENSESTG00000029924 ENSESTT00000075441 Transcript intron_variant - - - - - - rs12693469 2:188301732 A ENSESTG00000029924 ENSESTT00000075518 Transcript intron_variant - - - - - - rs6731444 2:188305335 G ENSESTG00000029924 ENSESTT00000075476 Transcript intron_variant - - - - - - rs6731444 2:188305335 G ENSESTG00000029924 ENSESTT00000075427 Transcript intron_variant - - - - - - rs6731444 2:188305335 G 10203 NM_005795.4 Transcript intron_variant - - - - - - rs6731444 2:188305335 G ENSESTG00000029924 ENSESTT00000075342 Transcript intron_variant - - - - - - rs6731444 2:188305335 G ENSESTG00000029924 ENSESTT00000075441 Transcript intron_variant - - - - - - rs6731444 2:188305335 G ENSESTG00000029924 ENSESTT00000075518 Transcript intron_variant - - - - - - rs2063504 2:188327001 A - ENSR00001046480 RegulatoryFeature regulatory_region_variant - - - - - - rs2063504 2:188327001 A 7035 NM_006287.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1956 rs2063504 2:188327001 A CCDS2294.1 CCDS2294.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4662 rs10202762 2:188345012 G CCDS33349.1 CCDS33349.1 Transcript intron_variant - - - - - - rs10202762 2:188345012 G 7035 NM_006287.4 Transcript intron_variant - - - - - - rs10202762 2:188345012 G 7035 NM_001032281.2 Transcript intron_variant - - - - - - rs10202762 2:188345012 G CCDS2294.1 CCDS2294.1 Transcript intron_variant - - - - - - rs893748 2:188941703 C - ENSR00001549786 RegulatoryFeature regulatory_region_variant - - - - - - rs893748 2:188941703 C - - - intergenic_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070277 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070303 Transcript intron_variant - - - - - - rs10176625 2:189360013 T 51454 NM_001252669.1 Transcript intron_variant - - - - - - rs10176625 2:189360013 T 51454 NM_016315.3 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070213 Transcript intron_variant - - - - - - rs10176625 2:189360013 T CCDS58742.1 CCDS58742.1 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070321 Transcript intron_variant - - - - - - rs10176625 2:189360013 T 51454 NR_045562.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070263 Transcript intron_variant - - - - - - rs10176625 2:189360013 T 51454 NM_001252668.1 Transcript intron_variant - - - - - - rs10176625 2:189360013 T CCDS58743.1 CCDS58743.1 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070327 Transcript intron_variant - - - - - - rs10176625 2:189360013 T 51454 NR_045563.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10176625 2:189360013 T CCDS2295.1 CCDS2295.1 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070194 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070294 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070351 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070206 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070255 Transcript intron_variant - - - - - - rs10176625 2:189360013 T ENSESTG00000027879 ENSESTT00000070338 Transcript intron_variant - - - - - - rs1543151 2:189798704 T - - - intergenic_variant - - - - - - rs966603 2:190322547 A CCDS2298.1 CCDS2298.1 Transcript intron_variant - - - - - - rs966603 2:190322547 A 84128 NM_032168.1 Transcript intron_variant - - - - - - rs966603 2:190322547 A ENSESTG00000019834 ENSESTT00000050200 Transcript downstream_gene_variant - - - - - - DISTANCE=2073 rs966603 2:190322547 A ENSESTG00000020047 ENSESTT00000050235 Transcript intron_variant - - - - - - rs966603 2:190322547 A ENSESTG00000019834 ENSESTT00000050176 Transcript intron_variant - - - - - - rs966603 2:190322547 A ENSESTG00000019834 ENSESTT00000050205 Transcript upstream_gene_variant - - - - - - DISTANCE=708 rs2043935 2:190427569 G ENSESTG00000015395 ENSESTT00000038620 Transcript downstream_gene_variant - - - - - - DISTANCE=1245 rs2043935 2:190427569 G 30061 NM_014585.5 Transcript intron_variant - - - - - - rs2043935 2:190427569 G CCDS2299.1 CCDS2299.1 Transcript intron_variant - - - - - - rs4666779 2:190481291 T - - - intergenic_variant - - - - - - rs7607988 2:191078924 G - ENSR00001549972 RegulatoryFeature regulatory_region_variant - - - - - - rs7607988 2:191078924 G ENSESTG00000015290 ENSESTT00000038392 Transcript intron_variant - - - - - - rs7607988 2:191078924 G CCDS2304.1 CCDS2304.1 Transcript intron_variant - - - - - - rs7607988 2:191078924 G CCDS46475.1 CCDS46475.1 Transcript intron_variant - - - - - - rs7607988 2:191078924 G 26275 NM_198047.2 Transcript intron_variant - - - - - - rs7607988 2:191078924 G ENSESTG00000015290 ENSESTT00000038374 Transcript intron_variant - - - - - - rs7607988 2:191078924 G ENSESTG00000015290 ENSESTT00000038412 Transcript intron_variant - - - - - - rs7607988 2:191078924 G 26275 NM_014362.3 Transcript intron_variant - - - - - - rs7607988 2:191078924 G ENSESTG00000015290 ENSESTT00000038418 Transcript intron_variant - - - - - - rs7607988 2:191078924 G ENSESTG00000015290 ENSESTT00000038399 Transcript intron_variant - - - - - - rs7607988 2:191078924 G ENSESTG00000015290 ENSESTT00000038410 Transcript intron_variant - - - - - - rs7607988 2:191078924 G ENSESTG00000015290 ENSESTT00000038434 Transcript intron_variant - - - - - - rs2192009 2:191462285 G - - - intergenic_variant - - - - - - rs929567 2:191521282 C - ENSR00001550007 RegulatoryFeature regulatory_region_variant - - - - - - rs929567 2:191521282 C ENSESTG00000021541 ENSESTT00000054092 Transcript intron_variant - - - - - - rs929567 2:191521282 C ENSESTG00000021541 ENSESTT00000054072 Transcript intron_variant - - - - - - rs929567 2:191521282 C CCDS2307.1 CCDS2307.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2621 rs929567 2:191521282 C ENSESTG00000021541 ENSESTT00000054057 Transcript intron_variant - - - - - - rs929567 2:191521282 C 4664 NM_005966.3 Transcript intron_variant - - - - - - rs929567 2:191521282 C ENSESTG00000021541 ENSESTT00000054125 Transcript intron_variant - - - - - - rs929567 2:191521282 C ENSESTG00000021541 ENSESTT00000054156 Transcript upstream_gene_variant - - - - - - DISTANCE=2520 rs929567 2:191521282 C ENSESTG00000021541 ENSESTT00000054062 Transcript intron_variant - - - - - - rs6434409 2:191521580 C ENSESTG00000021541 ENSESTT00000054092 Transcript intron_variant - - - - - - rs6434409 2:191521580 C ENSESTG00000021541 ENSESTT00000054072 Transcript intron_variant - - - - - - rs6434409 2:191521580 C CCDS2307.1 CCDS2307.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2323 rs6434409 2:191521580 C ENSESTG00000021541 ENSESTT00000054057 Transcript intron_variant - - - - - - rs6434409 2:191521580 C 4664 NM_005966.3 Transcript intron_variant - - - - - - rs6434409 2:191521580 C ENSESTG00000021541 ENSESTT00000054125 Transcript intron_variant - - - - - - rs6434409 2:191521580 C ENSESTG00000021541 ENSESTT00000054156 Transcript upstream_gene_variant - - - - - - DISTANCE=2222 rs6434409 2:191521580 C ENSESTG00000021541 ENSESTT00000054062 Transcript intron_variant - - - - - - rs4241277 2:191975970 T CCDS2310.1 CCDS2310.1 Transcript intron_variant - - - - - - rs4241277 2:191975970 T 6775 NM_003151.3 Transcript intron_variant - - - - - - rs4241277 2:191975970 T 6775 NM_001243835.1 Transcript intron_variant - - - - - - rs4241277 2:191975970 T ENSESTG00000022166 ENSESTT00000055914 Transcript intron_variant - - - - - - rs6759420 2:191987511 T CCDS2310.1 CCDS2310.1 Transcript intron_variant - - - - - - rs6759420 2:191987511 T 6775 NM_003151.3 Transcript intron_variant - - - - - - rs6759420 2:191987511 T 6775 NM_001243835.1 Transcript intron_variant - - - - - - rs6759420 2:191987511 T ENSESTG00000022166 ENSESTT00000055914 Transcript intron_variant - - - - - - rs4594474 2:191990536 T CCDS2310.1 CCDS2310.1 Transcript intron_variant - - - - - - rs4594474 2:191990536 T 6775 NM_003151.3 Transcript intron_variant - - - - - - rs4594474 2:191990536 T 6775 NM_001243835.1 Transcript intron_variant - - - - - - rs4594474 2:191990536 T ENSESTG00000022166 ENSESTT00000055914 Transcript intron_variant - - - - - - rs7586790 2:191994313 G CCDS2310.1 CCDS2310.1 Transcript intron_variant - - - - - - rs7586790 2:191994313 G 6775 NM_003151.3 Transcript intron_variant - - - - - - rs7586790 2:191994313 G 6775 NM_001243835.1 Transcript intron_variant - - - - - - rs7586790 2:191994313 G ENSESTG00000022166 ENSESTT00000055914 Transcript intron_variant - - - - - - rs7586790 2:191994313 G ENSESTG00000022166 ENSESTT00000055927 Transcript downstream_gene_variant - - - - - - DISTANCE=1907 rs6434438 2:191994415 A CCDS2310.1 CCDS2310.1 Transcript intron_variant - - - - - - rs6434438 2:191994415 A 6775 NM_003151.3 Transcript intron_variant - - - - - - rs6434438 2:191994415 A 6775 NM_001243835.1 Transcript intron_variant - - - - - - rs6434438 2:191994415 A ENSESTG00000022166 ENSESTT00000055914 Transcript intron_variant - - - - - - rs6434438 2:191994415 A ENSESTG00000022166 ENSESTT00000055927 Transcript downstream_gene_variant - - - - - - DISTANCE=1805 rs7602468 2:192006678 C CCDS2310.1 CCDS2310.1 Transcript intron_variant - - - - - - rs7602468 2:192006678 C 6775 NM_003151.3 Transcript intron_variant - - - - - - rs7602468 2:192006678 C 6775 NM_001243835.1 Transcript intron_variant - - - - - - rs7602468 2:192006678 C ENSESTG00000022166 ENSESTT00000055914 Transcript intron_variant - - - - - - rs7602468 2:192006678 C ENSESTG00000022166 ENSESTT00000055927 Transcript intron_variant - - - - - - rs7589175 2:192007148 A CCDS2310.1 CCDS2310.1 Transcript intron_variant - - - - - - rs7589175 2:192007148 A 6775 NM_003151.3 Transcript intron_variant - - - - - - rs7589175 2:192007148 A 6775 NM_001243835.1 Transcript intron_variant - - - - - - rs7589175 2:192007148 A ENSESTG00000022166 ENSESTT00000055914 Transcript intron_variant - - - - - - rs7589175 2:192007148 A ENSESTG00000022166 ENSESTT00000055927 Transcript intron_variant - - - - - - rs4853547 2:192019758 G 6775 NM_003151.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3772 rs4853547 2:192019758 G 6775 NM_001243835.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3436 rs4853547 2:192019758 G ENSESTG00000022166 ENSESTT00000055914 Transcript upstream_gene_variant - - - - - - DISTANCE=3960 rs4853547 2:192019758 G ENSESTG00000022166 ENSESTT00000055927 Transcript upstream_gene_variant - - - - - - DISTANCE=4061 rs1454750 2:192030690 G - - - intergenic_variant - - - - - - rs4853552 2:192046930 A - - - intergenic_variant - - - - - - rs6727812 2:192099091 A ENSESTG00000022158 ENSESTT00000055827 Transcript intron_variant - - - - - - rs6706774 2:192114836 A - ENSR00000604511 RegulatoryFeature regulatory_region_variant - - - - - - rs6706774 2:192114836 A ENSESTG00000021894 ENSESTT00000055668 Transcript intron_variant - - - - - - rs6706774 2:192114836 A 4430 NM_012223.3 Transcript intron_variant - - - - - - rs6706774 2:192114836 A ENSESTG00000021894 ENSESTT00000055575 Transcript intron_variant - - - - - - rs6706774 2:192114836 A 4430 NM_001130158.1 Transcript intron_variant - - - - - - rs6706774 2:192114836 A ENSESTG00000021894 ENSESTT00000055627 Transcript intron_variant - - - - - - rs6706774 2:192114836 A ENSESTG00000022158 ENSESTT00000055827 Transcript upstream_gene_variant - - - - - - DISTANCE=4120 rs6706774 2:192114836 A ENSESTG00000021894 ENSESTT00000055521 Transcript intron_variant - - - - - - rs6706774 2:192114836 A ENSESTG00000021894 ENSESTT00000055545 Transcript intron_variant - - - - - - rs6706774 2:192114836 A ENSESTG00000021894 ENSESTT00000055651 Transcript intron_variant - - - - - - rs6706774 2:192114836 A 4430 NM_001161819.1 Transcript intron_variant - - - - - - rs938803 2:192327460 C - - - intergenic_variant - - - - - - rs2356958 2:193037108 C CCDS2314.1 CCDS2314.1 Transcript intron_variant - - - - - - rs2356958 2:193037108 C ENSESTG00000014305 ENSESTT00000035789 Transcript intron_variant - - - - - - rs2356958 2:193037108 C 23671 NM_016192.2 Transcript intron_variant - - - - - - rs6720048 2:193051542 G CCDS2314.1 CCDS2314.1 Transcript intron_variant - - - - - - rs6720048 2:193051542 G ENSESTG00000014305 ENSESTT00000035789 Transcript upstream_gene_variant - - - - - - DISTANCE=2331 rs6720048 2:193051542 G 23671 NM_016192.2 Transcript intron_variant - - - - - - rs2592275 2:193088284 G - - - intergenic_variant - - - - - - rs1446399 2:193128977 A - - - intergenic_variant - - - - - - rs2581235 2:193169727 T - - - intergenic_variant - - - - - - rs1348768 2:193205790 A - - - intergenic_variant - - - - - - rs777132 2:193237086 G - - - intergenic_variant - - - - - - rs1471774 2:193304872 C - - - intergenic_variant - - - - - - rs10175576 2:193332080 G - - - intergenic_variant - - - - - - rs7608967 2:193410050 G - - - intergenic_variant - - - - - - rs1949300 2:193413757 T - - - intergenic_variant - - - - - - rs1515339 2:193419543 A - - - intergenic_variant - - - - - - rs1252881 2:193512089 G ENSESTG00000021283 ENSESTT00000053506 Transcript upstream_gene_variant - - - - - - DISTANCE=1976 rs1252881 2:193512089 G ENSESTG00000021262 ENSESTT00000053373 Transcript downstream_gene_variant - - - - - - DISTANCE=1659 rs1252881 2:193512089 G ENSESTG00000021283 ENSESTT00000053516 Transcript upstream_gene_variant - - - - - - DISTANCE=1980 rs2033851 2:193560317 T - - - intergenic_variant - - - - - - rs6734975 2:193574274 T - - - intergenic_variant - - - - - - rs4306730 2:193648391 C - - - intergenic_variant - - - - - - rs1439665 2:193655660 T - - - intergenic_variant - - - - - - rs6707460 2:193687209 A - - - intergenic_variant - - - - - - rs974358 2:193736366 T - - - intergenic_variant - - - - - - rs1445540 2:193755894 A - - - intergenic_variant - - - - - - rs2357463 2:193820720 C - - - intergenic_variant - - - - - - rs28583677 2:193913904 A - - - intergenic_variant - - - - - - rs1271568 2:193979579 T ENSESTG00000021271 ENSESTT00000053386 Transcript intron_variant - - - - - - rs10737938 2:194076806 G ENSESTG00000021271 ENSESTT00000053386 Transcript intron_variant - - - - - - rs1837356 2:194090278 A ENSESTG00000021271 ENSESTT00000053386 Transcript intron_variant - - - - - - rs10171311 2:194145688 C ENSESTG00000021271 ENSESTT00000053386 Transcript downstream_gene_variant - - - - - - DISTANCE=3899 rs12472285 2:194156958 C - - - intergenic_variant - - - - - - rs2243502 2:194294164 T - - - intergenic_variant - - - - - - rs1550408 2:194302321 A - - - intergenic_variant - - - - - - rs2251567 2:194319010 T - - - intergenic_variant - - - - - - rs1371641 2:194372264 G - - - intergenic_variant - - - - - - rs908716 2:194868640 C - - - intergenic_variant - - - - - - rs6744812 2:194904578 G - - - intergenic_variant - - - - - - rs4297906 2:194926044 T - - - intergenic_variant - - - - - - rs6761954 2:194953783 G - - - intergenic_variant - - - - - - rs2139009 2:195025325 T - - - intergenic_variant - - - - - - rs4561681 2:195157299 T - - - intergenic_variant - - - - - - rs4365482 2:195183066 T - - - intergenic_variant - - - - - - rs1406020 2:195357835 G - - - intergenic_variant - - - - - - rs141035461 2:195408220 C - - - intergenic_variant - - - - - - rs12624169 2:195411074 C - - - intergenic_variant - - - - - - rs1358384 2:195413913 C - - - intergenic_variant - - - - - - rs10174986 2:195418107 T - - - intergenic_variant - - - - - - rs4423617 2:195428749 G - - - intergenic_variant - - - - - - rs6434696 2:195438148 A - - - intergenic_variant - - - - - - rs2264015 2:195469481 C - - - intergenic_variant - - - - - - rs2884938 2:195495289 G - - - intergenic_variant - - - - - - rs699312 2:195560422 C - - - intergenic_variant - - - - - - rs801291 2:195595696 A - - - intergenic_variant - - - - - - rs2191506 2:195682448 C - - - intergenic_variant - - - - - - rs10184664 2:195686837 A - - - intergenic_variant - - - - - - rs2360688 2:195690689 A - - - intergenic_variant - - - - - - rs6754533 2:195702008 T - - - intergenic_variant - - - - - - rs2361080 2:195730301 C - - - intergenic_variant - - - - - - rs6717234 2:195733659 A - - - intergenic_variant - - - - - - rs1453813 2:195738675 A - - - intergenic_variant - - - - - - rs1453812 2:195744263 A - - - intergenic_variant - - - - - - rs10190765 2:195750023 C - - - intergenic_variant - - - - - - rs1377651 2:195751814 T - - - intergenic_variant - - - - - - rs2361082 2:195752017 T - - - intergenic_variant - - - - - - rs2123741 2:195758877 C - - - intergenic_variant - - - - - - rs1453806 2:195765870 A - - - intergenic_variant - - - - - - rs2167954 2:195769715 C - - - intergenic_variant - - - - - - rs10207794 2:195771040 C - - - intergenic_variant - - - - - - rs12615246 2:195773437 G - - - intergenic_variant - - - - - - rs10164543 2:195775761 C - - - intergenic_variant - - - - - - rs4271783 2:195783558 C - - - intergenic_variant - - - - - - rs4850567 2:195785644 G - - - intergenic_variant - - - - - - rs1598038 2:195787193 A - - - intergenic_variant - - - - - - rs4297907 2:195792310 G - - - intergenic_variant - - - - - - rs1453801 2:195802407 T - - - intergenic_variant - - - - - - rs12053180 2:195819176 G - - - intergenic_variant - - - - - - rs1019844 2:195832433 C - - - intergenic_variant - - - - - - rs1083372 2:195970482 C - ENSR00000604780 RegulatoryFeature regulatory_region_variant - - - - - - rs1083372 2:195970482 C - - - intergenic_variant - - - - - - rs6414140 2:196008214 C - - - intergenic_variant - - - - - - rs6414146 2:196116933 G - ENSR00000604785 RegulatoryFeature regulatory_region_variant - - - - - - rs6414146 2:196116933 G - - - intergenic_variant - - - - - - rs777285 2:196162351 T - - - intergenic_variant - - - - - - rs940345 2:196198825 G - - - intergenic_variant - - - - - - rs12693764 2:196231452 T - - - intergenic_variant - - - - - - rs4850370 2:196458065 A - - - intergenic_variant - - - - - - rs4531947 2:196521531 C - ENSR00000306044 RegulatoryFeature regulatory_region_variant - - - - - - rs4531947 2:196521531 C ENSESTG00000024713 ENSESTT00000062682 Transcript upstream_gene_variant - - - - - - DISTANCE=409 rs4531947 2:196521531 C 57181 NM_020342.2 Transcript upstream_gene_variant - - - - - - DISTANCE=321 rs4531947 2:196521531 C 57181 NM_001127257.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1 rs1879098 2:196929752 T ENSESTG00000025080 ENSESTT00000063339 Transcript intron_variant - - - - - - rs1879098 2:196929752 T ENSESTG00000025080 ENSESTT00000063328 Transcript intron_variant - - - - - - rs1879098 2:196929752 T ENSESTG00000025080 ENSESTT00000063285 Transcript intron_variant - - - - - - rs1879098 2:196929752 T 56171 NM_018897.2 Transcript intron_variant - - - - - - rs1879098 2:196929752 T CCDS42794.1 CCDS42794.1 Transcript intron_variant - - - - - - rs12693783 2:196959560 A - - - intergenic_variant - - - - - - rs1519606 2:196972518 G - - - intergenic_variant - - - - - - rs7599036 2:196988160 G - - - intergenic_variant - - - - - - rs6756823 2:196998557 G CCDS2315.1 CCDS2315.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3614 rs6756823 2:196998557 G ENSESTG00000024833 ENSESTT00000062725 Transcript 5_prime_UTR_variant 261 - - - - - rs6756823 2:196998557 G 9262 NM_004226.3 Transcript 3_prime_UTR_variant 5057 - - - - - rs4850670 2:197020515 A CCDS2315.1 CCDS2315.1 Transcript intron_variant - - - - - - rs4850670 2:197020515 A ENSESTG00000025024 ENSESTT00000063228 Transcript intron_variant - - - - - - rs4850670 2:197020515 A ENSESTG00000025024 ENSESTT00000063221 Transcript intron_variant - - - - - - rs4850670 2:197020515 A 9262 NM_004226.3 Transcript intron_variant - - - - - - rs4850670 2:197020515 A ENSESTG00000025024 ENSESTT00000063259 Transcript intron_variant - - - - - - rs1519594 2:197023048 C CCDS2315.1 CCDS2315.1 Transcript intron_variant - - - - - - rs1519594 2:197023048 C ENSESTG00000025024 ENSESTT00000063228 Transcript intron_variant - - - - - - rs1519594 2:197023048 C ENSESTG00000025024 ENSESTT00000063221 Transcript intron_variant - - - - - - rs1519594 2:197023048 C 9262 NM_004226.3 Transcript intron_variant - - - - - - rs1519594 2:197023048 C ENSESTG00000025024 ENSESTT00000063259 Transcript intron_variant - - - - - - rs1519596 2:197023180 T CCDS2315.1 CCDS2315.1 Transcript intron_variant - - - - - - rs1519596 2:197023180 T ENSESTG00000025024 ENSESTT00000063228 Transcript intron_variant - - - - - - rs1519596 2:197023180 T ENSESTG00000025024 ENSESTT00000063221 Transcript intron_variant - - - - - - rs1519596 2:197023180 T 9262 NM_004226.3 Transcript intron_variant - - - - - - rs1519596 2:197023180 T ENSESTG00000025024 ENSESTT00000063259 Transcript intron_variant - - - - - - rs6723159 2:197218666 A ENSESTG00000024874 ENSESTT00000062861 Transcript intron_variant - - - - - - rs6723159 2:197218666 A ENSESTG00000024874 ENSESTT00000062819 Transcript intron_variant - - - - - - rs6723159 2:197218666 A CCDS33354.1 CCDS33354.1 Transcript intron_variant - - - - - - rs6723159 2:197218666 A 57520 NM_020760.1 Transcript intron_variant - - - - - - rs6434846 2:197239202 G ENSESTG00000024874 ENSESTT00000062819 Transcript intron_variant - - - - - - rs6434846 2:197239202 G CCDS33354.1 CCDS33354.1 Transcript intron_variant - - - - - - rs6434846 2:197239202 G 57520 NM_020760.1 Transcript intron_variant - - - - - - rs11676253 2:197249241 G ENSESTG00000024874 ENSESTT00000062819 Transcript intron_variant - - - - - - rs11676253 2:197249241 G CCDS33354.1 CCDS33354.1 Transcript intron_variant - - - - - - rs11676253 2:197249241 G 57520 NM_020760.1 Transcript intron_variant - - - - - - rs10182718 2:197254664 G - ENSR00000604951 RegulatoryFeature regulatory_region_variant - - - - - - rs10182718 2:197254664 G ENSESTG00000024874 ENSESTT00000062819 Transcript intron_variant - - - - - - rs10182718 2:197254664 G CCDS33354.1 CCDS33354.1 Transcript intron_variant - - - - - - rs10182718 2:197254664 G 57520 NM_020760.1 Transcript intron_variant - - - - - - rs1527785 2:197371144 T ENSESTG00000024874 ENSESTT00000062819 Transcript intron_variant - - - - - - rs1527785 2:197371144 T 57520 NM_020760.1 Transcript intron_variant - - - - - - rs6704897 2:197436406 C ENSESTG00000024874 ENSESTT00000062819 Transcript intron_variant - - - - - - rs6704897 2:197436406 C 57520 NM_020760.1 Transcript intron_variant - - - - - - rs2037335 2:197524705 C 284992 NM_001080539.1 Transcript intron_variant - - - - - - rs2037335 2:197524705 C ENSESTG00000002421 ENSESTT00000006021 Transcript intron_variant - - - - - - rs2037335 2:197524705 C CCDS46478.1 CCDS46478.1 Transcript intron_variant - - - - - - rs2037335 2:197524705 C ENSESTG00000002421 ENSESTT00000006013 Transcript intron_variant - - - - - - rs7591388 2:197529709 A 284992 NM_001080539.1 Transcript intron_variant - - - - - - rs7591388 2:197529709 A ENSESTG00000002421 ENSESTT00000006021 Transcript intron_variant - - - - - - rs7591388 2:197529709 A CCDS46478.1 CCDS46478.1 Transcript intron_variant - - - - - - rs7591388 2:197529709 A ENSESTG00000002421 ENSESTT00000006013 Transcript intron_variant - - - - - - rs332299 2:197758148 T ENSESTG00000002584 ENSESTT00000006442 Transcript intron_variant - - - - - - rs332299 2:197758148 T ENSESTG00000002584 ENSESTT00000006438 Transcript intron_variant - - - - - - rs332299 2:197758148 T 80055 NM_024989.3 Transcript intron_variant - - - - - - rs332299 2:197758148 T ENSESTG00000002584 ENSESTT00000006461 Transcript intron_variant - - - - - - rs332299 2:197758148 T CCDS2318.1 CCDS2318.1 Transcript intron_variant - - - - - - rs332299 2:197758148 T ENSESTG00000002584 ENSESTT00000006430 Transcript intron_variant - - - - - - rs2697308 2:198073865 T - ENSR00000605070 RegulatoryFeature regulatory_region_variant - - - - - - rs2697308 2:198073865 T ENSESTG00000002553 ENSESTT00000006319 Transcript intron_variant - - - - - - rs2697308 2:198073865 T 91526 NM_153697.2 Transcript intron_variant - - - - - - rs2697308 2:198073865 T 91526 NM_001195144.1 Transcript intron_variant - - - - - - rs2697308 2:198073865 T ENSESTG00000002553 ENSESTT00000006324 Transcript intron_variant - - - - - - rs2697308 2:198073865 T CCDS33355.2 CCDS33355.2 Transcript intron_variant - - - - - - rs996450 2:199121749 G - - - intergenic_variant - - - - - - rs886871 2:199214071 C - - - intergenic_variant - - - - - - rs2249756 2:199240691 G - - - intergenic_variant - - - - - - rs2190653 2:199252203 C - - - intergenic_variant - - - - - - rs2190651 2:199257986 G - - - intergenic_variant - - - - - - rs2727770 2:199277692 A - - - intergenic_variant - - - - - - rs10166742 2:199406569 C - - - intergenic_variant - - - - - - rs13010827 2:199408747 C - - - intergenic_variant - - - - - - rs1455340 2:199410201 A - ENSR00000605218 RegulatoryFeature regulatory_region_variant - - - - - - rs1455340 2:199410201 A - - - intergenic_variant - - - - - - rs1563309 2:199411205 C - - - intergenic_variant - - - - - - rs1455339 2:199413499 G - - - intergenic_variant - - - - - - rs10197715 2:199434945 A - - - intergenic_variant - - - - - - rs1455337 2:199436163 A - - - intergenic_variant - - - - - - rs1378408 2:199496183 C - - - intergenic_variant - - - - - - rs6716751 2:199502040 C - - - intergenic_variant - - - - - - rs1878670 2:199593955 A - - - intergenic_variant - - - - - - rs1400972 2:199646007 T - - - intergenic_variant - - - - - - rs2138989 2:199706314 A - - - intergenic_variant - - - - - - rs6434992 2:199824424 G ENSESTG00000020936 ENSESTT00000052521 Transcript intron_variant - - - - - - rs1451499 2:199970591 A - - - intergenic_variant - - - - - - rs2345455 2:200057959 T - - - intergenic_variant - - - - - - rs260757 2:200125863 G - - - intergenic_variant - - - - - - rs4343415 2:200252282 G 23314 NM_001172517.1 Transcript intron_variant - - - - - - rs4343415 2:200252282 G 23314 NM_015265.3 Transcript intron_variant - - - - - - rs4343415 2:200252282 G ENSESTG00000020871 ENSESTT00000052470 Transcript intron_variant - - - - - - rs4343415 2:200252282 G ENSESTG00000020871 ENSESTT00000052479 Transcript intron_variant - - - - - - rs4343415 2:200252282 G ENSESTG00000020871 ENSESTT00000052489 Transcript intron_variant - - - - - - rs4343415 2:200252282 G ENSESTG00000020871 ENSESTT00000052412 Transcript intron_variant - - - - - - rs4343415 2:200252282 G ENSESTG00000020871 ENSESTT00000052495 Transcript intron_variant - - - - - - rs4343415 2:200252282 G 23314 NM_001172509.1 Transcript intron_variant - - - - - - rs4343415 2:200252282 G CCDS2327.1 CCDS2327.1 Transcript intron_variant - - - - - - rs4343415 2:200252282 G ENSESTG00000020871 ENSESTT00000052440 Transcript intron_variant - - - - - - rs1396971 2:200877332 G - - - intergenic_variant - - - - - - rs295151 2:201168703 C 26010 NM_001100422.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2282 rs295151 2:201168703 C ENSESTG00000026604 ENSESTT00000067015 Transcript upstream_gene_variant - - - - - - DISTANCE=2303 rs295151 2:201168703 C 26010 NM_015535.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1901 rs295151 2:201168703 C ENSESTG00000026604 ENSESTT00000067213 Transcript upstream_gene_variant - - - - - - DISTANCE=2544 rs295151 2:201168703 C ENSESTG00000026604 ENSESTT00000067224 Transcript upstream_gene_variant - - - - - - DISTANCE=2750 rs295151 2:201168703 C ENSESTG00000026604 ENSESTT00000067209 Transcript upstream_gene_variant - - - - - - DISTANCE=2544 rs295151 2:201168703 C ENSESTG00000026604 ENSESTT00000067215 Transcript upstream_gene_variant - - - - - - DISTANCE=2544 rs295151 2:201168703 C 26010 NM_001100424.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2282 rs295151 2:201168703 C ENSESTG00000026604 ENSESTT00000067226 Transcript upstream_gene_variant - - - - - - DISTANCE=2750 rs295151 2:201168703 C 26010 NM_001100423.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2653 rs2470898 2:201494474 C ENSESTG00000022712 ENSESTT00000057801 Transcript intron_variant - - - - - - rs2470898 2:201494474 C ENSESTG00000022712 ENSESTT00000057810 Transcript intron_variant - - - - - - rs2470898 2:201494474 C ENSESTG00000022712 ENSESTT00000057776 Transcript intron_variant - - - - - - rs2470898 2:201494474 C ENSESTG00000022712 ENSESTT00000057795 Transcript intron_variant - - - - - - rs2470898 2:201494474 C ENSESTG00000022712 ENSESTT00000057829 Transcript intron_variant - - - - - - rs2470898 2:201494474 C CCDS33360.1 CCDS33360.1 Transcript intron_variant - - - - - - rs2470898 2:201494474 C 316 NM_001159.3 Transcript intron_variant - - - - - - rs2470898 2:201494474 C ENSESTG00000022712 ENSESTT00000057813 Transcript intron_variant - - - - - - rs2470898 2:201494474 C ENSESTG00000022712 ENSESTT00000057760 Transcript intron_variant - - - - - - rs2470898 2:201494474 C ENSESTG00000022712 ENSESTT00000057847 Transcript intron_variant - - - - - - rs2080317 2:202390586 C CCDS54430.1 CCDS54430.1 Transcript intron_variant - - - - - - rs2080317 2:202390586 C CCDS54428.1 CCDS54428.1 Transcript intron_variant - - - - - - rs2080317 2:202390586 C 151254 NM_001168221.1 Transcript intron_variant - - - - - - rs2080317 2:202390586 C ENSESTG00000028321 ENSESTT00000071355 Transcript intron_variant - - - - - - rs2080317 2:202390586 C 151254 NM_152525.5 Transcript intron_variant - - - - - - rs2080317 2:202390586 C CCDS2349.1 CCDS2349.1 Transcript intron_variant - - - - - - rs2080317 2:202390586 C 151254 NM_001168216.1 Transcript intron_variant - - - - - - rs6727377 2:202539295 C ENSESTG00000028298 ENSESTT00000071184 Transcript intron_variant - - - - - - rs6727377 2:202539295 C CCDS46491.1 CCDS46491.1 Transcript intron_variant - - - - - - rs6727377 2:202539295 C 58538 NM_033066.2 Transcript intron_variant - - - - - - rs10193416 2:202644392 T 57679 NM_001135745.1 Transcript intron_variant - - - - - - rs10193416 2:202644392 T 57679 NM_020919.3 Transcript intron_variant - - - - - - rs929628 2:202662046 A - ENSR00001550676 RegulatoryFeature regulatory_region_variant - - - - - - rs929628 2:202662046 A - - - intergenic_variant - - - - - - rs3937458 2:202675171 T CCDS2350.1 CCDS2350.1 Transcript intron_variant - - - - - - rs3937458 2:202675171 T ENSESTG00000027924 ENSESTT00000070398 Transcript intron_variant - - - - - - rs3937458 2:202675171 T 65061 NM_001261435.1 Transcript intron_variant - - - - - - rs3937458 2:202675171 T CCDS58746.1 CCDS58746.1 Transcript intron_variant - - - - - - rs3937458 2:202675171 T 65061 NM_139158.2 Transcript intron_variant - - - - - - rs3937458 2:202675171 T CCDS58747.1 CCDS58747.1 Transcript intron_variant - - - - - - rs3937458 2:202675171 T ENSESTG00000027924 ENSESTT00000070384 Transcript intron_variant - - - - - - rs3937458 2:202675171 T ENSESTG00000027924 ENSESTT00000070405 Transcript intron_variant - - - - - - rs3937458 2:202675171 T 65061 NM_001261436.1 Transcript intron_variant - - - - - - rs4140771 2:202726974 C CCDS2350.1 CCDS2350.1 Transcript intron_variant - - - - - - rs4140771 2:202726974 C 65061 NM_001261435.1 Transcript intron_variant - - - - - - rs4140771 2:202726974 C ENSESTG00000027924 ENSESTT00000070475 Transcript intron_variant - - - - - - rs4140771 2:202726974 C CCDS58746.1 CCDS58746.1 Transcript intron_variant - - - - - - rs4140771 2:202726974 C ENSESTG00000027924 ENSESTT00000070434 Transcript intron_variant - - - - - - rs4140771 2:202726974 C ENSESTG00000027924 ENSESTT00000070468 Transcript intron_variant - - - - - - rs4140771 2:202726974 C 65061 NM_139158.2 Transcript intron_variant - - - - - - rs4140771 2:202726974 C CCDS58747.1 CCDS58747.1 Transcript intron_variant - - - - - - rs4140771 2:202726974 C 65061 NM_001261436.1 Transcript intron_variant - - - - - - rs10931977 2:202734402 C CCDS2350.1 CCDS2350.1 Transcript intron_variant - - - - - - rs10931977 2:202734402 C 65061 NM_001261435.1 Transcript intron_variant - - - - - - rs10931977 2:202734402 C ENSESTG00000027924 ENSESTT00000070475 Transcript intron_variant - - - - - - rs10931977 2:202734402 C CCDS58746.1 CCDS58746.1 Transcript intron_variant - - - - - - rs10931977 2:202734402 C ENSESTG00000027924 ENSESTT00000070434 Transcript intron_variant - - - - - - rs10931977 2:202734402 C ENSESTG00000027924 ENSESTT00000070468 Transcript intron_variant - - - - - - rs10931977 2:202734402 C 65061 NM_139158.2 Transcript intron_variant - - - - - - rs10931977 2:202734402 C CCDS58747.1 CCDS58747.1 Transcript intron_variant - - - - - - rs10931977 2:202734402 C 65061 NM_001261436.1 Transcript intron_variant - - - - - - rs759418 2:202779191 A - - - intergenic_variant - - - - - - rs6435198 2:204519416 G ENSESTG00000002627 ENSESTT00000006522 Transcript intron_variant - - - - - - rs4675392 2:204845640 A - - - intergenic_variant - - - - - - rs10210708 2:204873027 G - - - intergenic_variant - - - - - - rs965111 2:206342766 C 117583 NM_152526.5 Transcript intron_variant - - - - - - rs965111 2:206342766 C 117583 NM_057177.6 Transcript intron_variant - - - - - - rs965111 2:206342766 C CCDS42804.1 CCDS42804.1 Transcript intron_variant - - - - - - rs965111 2:206342766 C CCDS42805.1 CCDS42805.1 Transcript intron_variant - - - - - - rs965111 2:206342766 C CCDS42806.1 CCDS42806.1 Transcript intron_variant - - - - - - rs965111 2:206342766 C 117583 NM_205863.3 Transcript intron_variant - - - - - - rs1990849 2:207621759 G 130752 NM_001039845.1 Transcript synonymous_variant 331 276 92 Y taT/taC - rs1990849 2:207621759 G CCDS33365.1 CCDS33365.1 Transcript synonymous_variant 276 276 92 Y taT/taC - rs6741063 2:207889001 G - - - intergenic_variant - - - - - - rs1263633 2:207933801 C - - - intergenic_variant - - - - - - rs11683102 2:208075915 T ENSESTG00000004384 ENSESTT00000011102 Transcript intron_variant - - - - - - rs6435377 2:208263911 C - - - intergenic_variant - - - - - - rs2718657 2:208742975 T ENSESTG00000020384 ENSESTT00000051169 Transcript intron_variant - - - - - - rs2718657 2:208742975 T ENSESTG00000020384 ENSESTT00000051149 Transcript intron_variant - - - - - - rs2718657 2:208742975 T CCDS42808.1 CCDS42808.1 Transcript intron_variant - - - - - - rs2718657 2:208742975 T ENSESTG00000020384 ENSESTT00000051198 Transcript intron_variant - - - - - - rs2718657 2:208742975 T 389072 NM_001080475.2 Transcript intron_variant - - - - - - rs2100350 2:208850307 T CCDS42808.1 CCDS42808.1 Transcript intron_variant - - - - - - rs2100350 2:208850307 T 389072 NM_001080475.2 Transcript intron_variant - - - - - - rs4673405 2:209270705 T 5746 NM_005048.2 Transcript upstream_gene_variant - - - - - - DISTANCE=851 rs4673405 2:209270705 T ENSESTG00000020200 ENSESTT00000050672 Transcript intron_variant - - - - - - rs4673405 2:209270705 T ENSESTG00000020200 ENSESTT00000050661 Transcript intron_variant - - - - - - rs4673405 2:209270705 T CCDS2383.1 CCDS2383.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1064 rs4673405 2:209270705 T ENSESTG00000020200 ENSESTT00000050686 Transcript upstream_gene_variant - - - - - - DISTANCE=1063 rs1031485 2:209473632 A - ENSR00000306557 RegulatoryFeature regulatory_region_variant - - - - - - rs1031485 2:209473632 A ENSESTG00000007256 ENSESTT00000018295 Transcript intron_variant - - - - - - rs7608369 2:209580098 T ENSESTG00000007256 ENSESTT00000018295 Transcript intron_variant - - - - - - rs2084210 2:210148733 C ENSESTG00000007277 ENSESTT00000018343 Transcript intron_variant - - - - - - rs1473331 2:210178052 C ENSESTG00000007277 ENSESTT00000018343 Transcript intron_variant - - - - - - rs6751262 2:210234118 A - ENSR00001551202 RegulatoryFeature regulatory_region_variant - - - - - - rs6751262 2:210234118 A ENSESTG00000007277 ENSESTT00000018343 Transcript intron_variant - - - - - - rs2365660 2:210355012 G 4133 NM_001039538.1 Transcript intron_variant - - - - - - rs2365660 2:210355012 G ENSESTG00000007261 ENSESTT00000018334 Transcript intron_variant - - - - - - rs288090 2:210396262 C 4133 NM_001039538.1 Transcript intron_variant - - - - - - rs288090 2:210396262 C ENSESTG00000007261 ENSESTT00000018334 Transcript intron_variant - - - - - - rs2544309 2:211399066 T CCDS46505.1 CCDS46505.1 Transcript intron_variant - - - - - - rs2544309 2:211399066 T ENSESTG00000006237 ENSESTT00000015765 Transcript intron_variant - - - - - - rs2544309 2:211399066 T ENSESTG00000006237 ENSESTT00000015757 Transcript intron_variant - - - - - - rs2544309 2:211399066 T 1373 NM_001122633.2 Transcript intron_variant - - - - - - rs4673540 2:211513118 T ENSESTG00000006275 ENSESTT00000015847 Transcript upstream_gene_variant - - - - - - DISTANCE=1411 rs4673540 2:211513118 T CCDS46505.1 CCDS46505.1 Transcript intron_variant - - - - - - rs4673540 2:211513118 T CCDS2393.1 CCDS2393.1 Transcript intron_variant - - - - - - rs4673540 2:211513118 T CCDS46506.1 CCDS46506.1 Transcript intron_variant - - - - - - rs4673540 2:211513118 T 1373 NM_001875.4 Transcript intron_variant - - - - - - rs4673540 2:211513118 T ENSESTG00000006275 ENSESTT00000015833 Transcript intron_variant - - - - - - rs4673540 2:211513118 T ENSESTG00000006275 ENSESTT00000015831 Transcript intron_variant - - - - - - rs4673540 2:211513118 T ENSESTG00000006275 ENSESTT00000015836 Transcript intron_variant - - - - - - rs4673540 2:211513118 T 1373 NM_001122633.2 Transcript intron_variant - - - - - - rs4673540 2:211513118 T ENSESTG00000006275 ENSESTT00000015843 Transcript intron_variant - - - - - - rs4673540 2:211513118 T ENSESTG00000006275 ENSESTT00000015842 Transcript intron_variant - - - - - - rs4673540 2:211513118 T ENSESTG00000006275 ENSESTT00000015834 Transcript intron_variant - - - - - - rs4673540 2:211513118 T 1373 NM_001122634.2 Transcript intron_variant - - - - - - rs6435579 2:211522889 T ENSESTG00000006275 ENSESTT00000015847 Transcript intron_variant - - - - - - rs6435579 2:211522889 T CCDS46505.1 CCDS46505.1 Transcript intron_variant - - - - - - rs6435579 2:211522889 T CCDS2393.1 CCDS2393.1 Transcript intron_variant - - - - - - rs6435579 2:211522889 T CCDS46506.1 CCDS46506.1 Transcript intron_variant - - - - - - rs6435579 2:211522889 T 1373 NM_001875.4 Transcript intron_variant - - - - - - rs6435579 2:211522889 T ENSESTG00000006275 ENSESTT00000015833 Transcript downstream_gene_variant - - - - - - DISTANCE=1522 rs6435579 2:211522889 T ENSESTG00000006275 ENSESTT00000015831 Transcript intron_variant - - - - - - rs6435579 2:211522889 T ENSESTG00000006275 ENSESTT00000015836 Transcript downstream_gene_variant - - - - - - DISTANCE=1522 rs6435579 2:211522889 T 1373 NM_001122633.2 Transcript intron_variant - - - - - - rs6435579 2:211522889 T ENSESTG00000006275 ENSESTT00000015843 Transcript downstream_gene_variant - - - - - - DISTANCE=1522 rs6435579 2:211522889 T ENSESTG00000006275 ENSESTT00000015842 Transcript intron_variant - - - - - - rs6435579 2:211522889 T ENSESTG00000006275 ENSESTT00000015834 Transcript intron_variant - - - - - - rs6435579 2:211522889 T 1373 NM_001122634.2 Transcript intron_variant - - - - - - rs2371014 2:211546223 T ENSESTG00000006298 ENSESTT00000015870 Transcript downstream_gene_variant - - - - - - DISTANCE=3051 rs2371014 2:211546223 T CCDS46505.1 CCDS46505.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3514 rs2371014 2:211546223 T CCDS2393.1 CCDS2393.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3514 rs2371014 2:211546223 T CCDS46506.1 CCDS46506.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3514 rs2371014 2:211546223 T 1373 NM_001875.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2392 rs2371014 2:211546223 T 1373 NM_001122634.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2392 rs2371014 2:211546223 T 1373 NM_001122633.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2392 rs2371017 2:211553023 G - - - intergenic_variant - - - - - - rs7572869 2:211553722 T - - - intergenic_variant - - - - - - rs10201983 2:211608344 A - - - intergenic_variant - - - - - - rs6435584 2:211645245 G - - - intergenic_variant - - - - - - rs4672597 2:211648925 G - - - intergenic_variant - - - - - - rs2887933 2:211666837 G - - - intergenic_variant - - - - - - rs2371083 2:211667250 G - - - intergenic_variant - - - - - - rs1014698 2:211678351 C - - - intergenic_variant - - - - - - rs2371084 2:211680883 C - - - intergenic_variant - - - - - - rs796247 2:211818552 G - - - intergenic_variant - - - - - - rs615893 2:211823682 C - - - intergenic_variant - - - - - - rs1837053 2:211830637 C - - - intergenic_variant - - - - - - rs378083 2:211845335 T - - - intergenic_variant - - - - - - rs473035 2:211885709 T - - - intergenic_variant - - - - - - rs319720 2:211892845 A - - - intergenic_variant - - - - - - rs223275 2:211922378 G - - - intergenic_variant - - - - - - rs707279 2:211967805 A - - - intergenic_variant - - - - - - rs7590561 2:212013333 C - - - intergenic_variant - - - - - - rs6435603 2:212021114 A - - - intergenic_variant - - - - - - rs12614480 2:212031661 G - - - intergenic_variant - - - - - - rs6760353 2:212058077 A - - - intergenic_variant - - - - - - rs1437923 2:212061356 T - - - intergenic_variant - - - - - - rs1898566 2:212063262 A - - - intergenic_variant - - - - - - rs2371174 2:212070191 C - ENSR00000606646 RegulatoryFeature regulatory_region_variant - - - - - - rs2371174 2:212070191 C - - - intergenic_variant - - - - - - rs1370607 2:212083505 T - - - intergenic_variant - - - - - - rs1347714 2:212118313 T - - - intergenic_variant - - - - - - rs12996011 2:212128568 C - - - intergenic_variant - - - - - - rs4673605 2:212129811 C - - - intergenic_variant - - - - - - rs1965121 2:212283124 T 2066 NM_005235.2 Transcript intron_variant - - - - - - rs1965121 2:212283124 T CCDS2394.1 CCDS2394.1 Transcript intron_variant - - - - - - rs1965121 2:212283124 T CCDS42811.1 CCDS42811.1 Transcript intron_variant - - - - - - rs1965121 2:212283124 T 2066 NM_001042599.1 Transcript intron_variant - - - - - - rs6435640 2:212427277 T 2066 NM_005235.2 Transcript intron_variant - - - - - - rs6435640 2:212427277 T ENSESTG00000019558 ENSESTT00000049064 Transcript intron_variant - - - - - - rs6435640 2:212427277 T CCDS2394.1 CCDS2394.1 Transcript intron_variant - - - - - - rs6435640 2:212427277 T ENSESTG00000006304 ENSESTT00000015878 Transcript upstream_gene_variant - - - - - - DISTANCE=579 rs6435640 2:212427277 T CCDS42811.1 CCDS42811.1 Transcript intron_variant - - - - - - rs6435640 2:212427277 T 2066 NM_001042599.1 Transcript intron_variant - - - - - - rs7564309 2:212432507 G 2066 NM_005235.2 Transcript intron_variant - - - - - - rs7564309 2:212432507 G ENSESTG00000019558 ENSESTT00000049064 Transcript intron_variant - - - - - - rs7564309 2:212432507 G CCDS2394.1 CCDS2394.1 Transcript intron_variant - - - - - - rs7564309 2:212432507 G CCDS42811.1 CCDS42811.1 Transcript intron_variant - - - - - - rs7564309 2:212432507 G 2066 NM_001042599.1 Transcript intron_variant - - - - - - rs1347888 2:212785301 A 2066 NM_005235.2 Transcript intron_variant - - - - - - rs1347888 2:212785301 A ENSESTG00000019459 ENSESTT00000048913 Transcript intron_variant - - - - - - rs1347888 2:212785301 A CCDS2394.1 CCDS2394.1 Transcript intron_variant - - - - - - rs1347888 2:212785301 A ENSESTG00000019459 ENSESTT00000048902 Transcript intron_variant - - - - - - rs1347888 2:212785301 A CCDS42811.1 CCDS42811.1 Transcript intron_variant - - - - - - rs1347888 2:212785301 A 2066 NM_001042599.1 Transcript intron_variant - - - - - - rs2371478 2:213064735 C 2066 NM_005235.2 Transcript intron_variant - - - - - - rs2371478 2:213064735 C CCDS2394.1 CCDS2394.1 Transcript intron_variant - - - - - - rs2371478 2:213064735 C CCDS42811.1 CCDS42811.1 Transcript intron_variant - - - - - - rs2371478 2:213064735 C 2066 NM_001042599.1 Transcript intron_variant - - - - - - rs894116 2:213955891 C ENSESTG00000001559 ENSESTT00000003689 Transcript intron_variant - - - - - - rs894116 2:213955891 C CCDS2395.1 CCDS2395.1 Transcript intron_variant - - - - - - rs894116 2:213955891 C ENSESTG00000001559 ENSESTT00000003692 Transcript intron_variant - - - - - - rs894116 2:213955891 C 22807 NM_016260.2 Transcript intron_variant - - - - - - rs894116 2:213955891 C ENSESTG00000001559 ENSESTT00000003681 Transcript intron_variant - - - - - - rs894116 2:213955891 C ENSESTG00000001559 ENSESTT00000003684 Transcript intron_variant - - - - - - rs894116 2:213955891 C ENSESTG00000001559 ENSESTT00000003700 Transcript intron_variant - - - - - - rs894116 2:213955891 C CCDS46507.1 CCDS46507.1 Transcript intron_variant - - - - - - rs894116 2:213955891 C 22807 NM_001079526.1 Transcript intron_variant - - - - - - rs2216488 2:215026803 T 79582 NM_024532.4 Transcript intron_variant - - - - - - rs2216488 2:215026803 T 79582 NR_047660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2216488 2:215026803 T CCDS2396.1 CCDS2396.1 Transcript intron_variant - - - - - - rs2216488 2:215026803 T 79582 NR_047659.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1912207 2:215102929 A 79582 NM_024532.4 Transcript intron_variant - - - - - - rs1912207 2:215102929 A 79582 NR_047660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1912207 2:215102929 A CCDS2396.1 CCDS2396.1 Transcript intron_variant - - - - - - rs1912207 2:215102929 A 79582 NR_047659.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2052441 2:215107598 A - ENSR00000606873 RegulatoryFeature regulatory_region_variant - - - - - - rs2052441 2:215107598 A 79582 NM_024532.4 Transcript intron_variant - - - - - - rs2052441 2:215107598 A 79582 NR_047660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2052441 2:215107598 A CCDS2396.1 CCDS2396.1 Transcript intron_variant - - - - - - rs2052441 2:215107598 A 79582 NR_047659.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs976911 2:215110139 A 79582 NM_024532.4 Transcript intron_variant - - - - - - rs976911 2:215110139 A 79582 NR_047660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs976911 2:215110139 A CCDS2396.1 CCDS2396.1 Transcript intron_variant - - - - - - rs976911 2:215110139 A 79582 NR_047659.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1912193 2:215161203 A 79582 NM_024532.4 Transcript intron_variant - - - - - - rs1912193 2:215161203 A 79582 NR_047660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1912193 2:215161203 A CCDS2396.1 CCDS2396.1 Transcript intron_variant - - - - - - rs1912193 2:215161203 A 79582 NR_047659.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10166554 2:215240104 A 79582 NM_024532.4 Transcript intron_variant - - - - - - rs10166554 2:215240104 A 79582 NR_047660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10166554 2:215240104 A CCDS2396.1 CCDS2396.1 Transcript intron_variant - - - - - - rs10166554 2:215240104 A 79582 NR_047659.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4283423 2:215255018 C 79582 NM_024532.4 Transcript intron_variant - - - - - - rs4283423 2:215255018 C 79582 NR_047660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4283423 2:215255018 C CCDS2396.1 CCDS2396.1 Transcript intron_variant - - - - - - rs4283423 2:215255018 C 79582 NR_047659.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6719752 2:215258922 G 79582 NM_024532.4 Transcript intron_variant - - - - - - rs6719752 2:215258922 G 79582 NR_047660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6719752 2:215258922 G CCDS2396.1 CCDS2396.1 Transcript intron_variant - - - - - - rs6719752 2:215258922 G 79582 NR_047659.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7560617 2:215304213 T 402117 NM_001080500.2 Transcript intron_variant - - - - - - rs7560617 2:215304213 T CCDS46509.1 CCDS46509.1 Transcript intron_variant - - - - - - rs7560617 2:215304213 T ENSESTG00000009844 ENSESTT00000024617 Transcript intron_variant - - - - - - rs10804228 2:215305557 T 402117 NM_001080500.2 Transcript intron_variant - - - - - - rs10804228 2:215305557 T CCDS46509.1 CCDS46509.1 Transcript intron_variant - - - - - - rs10804228 2:215305557 T ENSESTG00000009844 ENSESTT00000024617 Transcript intron_variant - - - - - - rs12478648 2:215369048 A 402117 NM_001080500.2 Transcript intron_variant - - - - - - rs12478648 2:215369048 A CCDS46509.1 CCDS46509.1 Transcript intron_variant - - - - - - rs12478648 2:215369048 A ENSESTG00000009844 ENSESTT00000024617 Transcript intron_variant - - - - - - rs4233998 2:215384278 G - ENSR00001046800 RegulatoryFeature regulatory_region_variant - - - - - - rs4233998 2:215384278 G 402117 NM_001080500.2 Transcript intron_variant - - - - - - rs4233998 2:215384278 G ENSESTG00000023240 ENSESTT00000058652 Transcript intron_variant - - - - - - rs4233998 2:215384278 G CCDS46509.1 CCDS46509.1 Transcript intron_variant - - - - - - rs4233998 2:215384278 G ENSESTG00000009844 ENSESTT00000024617 Transcript intron_variant - - - - - - rs4233998 2:215384278 G 100885780 NR_047698.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4673852 2:215387444 C 402117 NM_001080500.2 Transcript intron_variant - - - - - - rs4673852 2:215387444 C ENSESTG00000023240 ENSESTT00000058652 Transcript intron_variant - - - - - - rs4673852 2:215387444 C CCDS46509.1 CCDS46509.1 Transcript intron_variant - - - - - - rs4673852 2:215387444 C ENSESTG00000009844 ENSESTT00000024617 Transcript intron_variant - - - - - - rs4673852 2:215387444 C 100885780 NR_047698.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4517971 2:215507101 T - - - intergenic_variant - - - - - - rs6749882 2:215520235 T - - - intergenic_variant - - - - - - rs10192590 2:215547061 G - - - intergenic_variant - - - - - - rs280635 2:215561005 C - - - intergenic_variant - - - - - - rs7585121 2:215592290 G ENSESTG00000024054 ENSESTT00000060884 Transcript downstream_gene_variant - - - - - - DISTANCE=987 rs7585121 2:215592290 G CCDS2397.1 CCDS2397.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1110 rs7585121 2:215592290 G 580 NM_000465.2 Transcript downstream_gene_variant - - - - - - DISTANCE=972 rs6435849 2:215595765 G ENSESTG00000024054 ENSESTT00000060884 Transcript intron_variant - - - - - - rs6435849 2:215595765 G CCDS2397.1 CCDS2397.1 Transcript intron_variant - - - - - - rs6435849 2:215595765 G 580 NM_000465.2 Transcript intron_variant - - - - - - rs10804234 2:215600080 C ENSESTG00000024054 ENSESTT00000060884 Transcript intron_variant - - - - - - rs10804234 2:215600080 C CCDS2397.1 CCDS2397.1 Transcript intron_variant - - - - - - rs10804234 2:215600080 C 580 NM_000465.2 Transcript intron_variant - - - - - - rs10932567 2:215602949 A ENSESTG00000024054 ENSESTT00000060884 Transcript intron_variant - - - - - - rs10932567 2:215602949 A CCDS2397.1 CCDS2397.1 Transcript intron_variant - - - - - - rs10932567 2:215602949 A 580 NM_000465.2 Transcript intron_variant - - - - - - rs2034252 2:215606726 G ENSESTG00000024054 ENSESTT00000060884 Transcript intron_variant - - - - - - rs2034252 2:215606726 G CCDS2397.1 CCDS2397.1 Transcript intron_variant - - - - - - rs2034252 2:215606726 G 580 NM_000465.2 Transcript intron_variant - - - - - - rs2034252 2:215606726 G ENSESTG00000024054 ENSESTT00000060899 Transcript downstream_gene_variant - - - - - - DISTANCE=3710 rs4088306 2:215640911 A - ENSR00001551446 RegulatoryFeature regulatory_region_variant - - - - - - rs4088306 2:215640911 A ENSESTG00000024054 ENSESTT00000060884 Transcript intron_variant - - - - - - rs4088306 2:215640911 A CCDS2397.1 CCDS2397.1 Transcript intron_variant - - - - - - rs4088306 2:215640911 A 580 NM_000465.2 Transcript intron_variant - - - - - - rs4088306 2:215640911 A ENSESTG00000024054 ENSESTT00000060899 Transcript intron_variant - - - - - - rs2121286 2:215692125 C - - - intergenic_variant - - - - - - rs4571053 2:215701363 G - - - intergenic_variant - - - - - - rs6728876 2:215703452 G - - - intergenic_variant - - - - - - rs777327 2:215742170 A - - - intergenic_variant - - - - - - rs12477655 2:215771036 G - - - intergenic_variant - - - - - - rs7583785 2:215838361 G CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs7583785 2:215838361 G ENSESTG00000023968 ENSESTT00000060480 Transcript intron_variant - - - - - - rs7583785 2:215838361 G CCDS33373.1 CCDS33373.1 Transcript intron_variant - - - - - - rs7583785 2:215838361 G 26154 NM_015657.3 Transcript intron_variant - - - - - - rs7583785 2:215838361 G ENSESTG00000023968 ENSESTT00000060524 Transcript intron_variant - - - - - - rs7583785 2:215838361 G 26154 NM_173076.2 Transcript intron_variant - - - - - - rs10195034 2:215841649 G CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs10195034 2:215841649 G ENSESTG00000023968 ENSESTT00000060480 Transcript upstream_gene_variant - - - - - - DISTANCE=1001 rs10195034 2:215841649 G CCDS33373.1 CCDS33373.1 Transcript intron_variant - - - - - - rs10195034 2:215841649 G 26154 NM_015657.3 Transcript intron_variant - - - - - - rs10195034 2:215841649 G ENSESTG00000023968 ENSESTT00000060524 Transcript upstream_gene_variant - - - - - - DISTANCE=2883 rs10195034 2:215841649 G 26154 NM_173076.2 Transcript intron_variant - - - - - - rs7608150 2:215848034 C CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs7608150 2:215848034 C CCDS33373.1 CCDS33373.1 Transcript intron_variant - - - - - - rs7608150 2:215848034 C 26154 NM_015657.3 Transcript intron_variant - - - - - - rs7608150 2:215848034 C 26154 NM_173076.2 Transcript intron_variant - - - - - - rs1409607 2:215875251 T CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs1409607 2:215875251 T CCDS33373.1 CCDS33373.1 Transcript intron_variant - - - - - - rs1409607 2:215875251 T 26154 NM_015657.3 Transcript intron_variant - - - - - - rs1409607 2:215875251 T 26154 NM_173076.2 Transcript intron_variant - - - - - - rs2177424 2:215890253 G CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs2177424 2:215890253 G CCDS33373.1 CCDS33373.1 Transcript intron_variant - - - - - - rs2177424 2:215890253 G ENSESTG00000023246 ENSESTT00000058695 Transcript downstream_gene_variant - - - - - - DISTANCE=2416 rs2177424 2:215890253 G ENSESTG00000023246 ENSESTT00000058685 Transcript intron_variant - - - - - - rs2177424 2:215890253 G 26154 NM_015657.3 Transcript intron_variant - - - - - - rs2177424 2:215890253 G 26154 NM_173076.2 Transcript intron_variant - - - - - - rs2177424 2:215890253 G ENSESTG00000023961 ENSESTT00000060451 Transcript intron_variant - - - - - - rs2091094 2:215898267 A CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs2091094 2:215898267 A CCDS33373.1 CCDS33373.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1616 rs2091094 2:215898267 A ENSESTG00000023246 ENSESTT00000058685 Transcript intron_variant - - - - - - rs2091094 2:215898267 A 26154 NM_015657.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1457 rs2091094 2:215898267 A 26154 NM_173076.2 Transcript intron_variant - - - - - - rs2204266 2:215911819 A CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs2204266 2:215911819 A 26154 NM_173076.2 Transcript intron_variant - - - - - - rs1523722 2:215920048 G CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs1523722 2:215920048 G 26154 NM_173076.2 Transcript intron_variant - - - - - - rs10932588 2:215928199 C CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs10932588 2:215928199 C 26154 NM_173076.2 Transcript intron_variant - - - - - - rs2140471 2:215932149 C CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs2140471 2:215932149 C 26154 NM_173076.2 Transcript intron_variant - - - - - - rs6740580 2:215936850 T - ENSR00001551456 RegulatoryFeature regulatory_region_variant - - - - - - rs6740580 2:215936850 T CCDS33372.1 CCDS33372.1 Transcript intron_variant - - - - - - rs6740580 2:215936850 T ENSESTG00000023952 ENSESTT00000060432 Transcript downstream_gene_variant - - - - - - DISTANCE=3366 rs6740580 2:215936850 T 26154 NM_173076.2 Transcript intron_variant - - - - - - rs12621030 2:216044080 G - - - intergenic_variant - - - - - - rs10192055 2:216044700 C - - - intergenic_variant - - - - - - rs10167673 2:216066247 T - - - intergenic_variant - - - - - - rs4673955 2:216067237 G - - - intergenic_variant - - - - - - rs7577531 2:216068825 T - - - intergenic_variant - - - - - - rs6435883 2:216074375 T - - - intergenic_variant - - - - - - rs12477386 2:216081070 T - - - intergenic_variant - - - - - - rs6745528 2:216114302 T - - - intergenic_variant - - - - - - rs6734892 2:216127372 A - - - intergenic_variant - - - - - - rs10185278 2:216137766 C - - - intergenic_variant - - - - - - rs7572061 2:216173455 T ENSESTG00000023266 ENSESTT00000059011 Transcript upstream_gene_variant - - - - - - DISTANCE=3398 rs7572061 2:216173455 T ENSESTG00000023266 ENSESTT00000058986 Transcript upstream_gene_variant - - - - - - DISTANCE=3398 rs7572061 2:216173455 T ENSESTG00000023266 ENSESTT00000059001 Transcript upstream_gene_variant - - - - - - DISTANCE=3398 rs7572061 2:216173455 T ENSESTG00000023266 ENSESTT00000058948 Transcript upstream_gene_variant - - - - - - DISTANCE=3360 rs7572061 2:216173455 T ENSESTG00000023266 ENSESTT00000059007 Transcript upstream_gene_variant - - - - - - DISTANCE=3398 rs7572061 2:216173455 T ENSESTG00000023266 ENSESTT00000058963 Transcript upstream_gene_variant - - - - - - DISTANCE=3360 rs7572061 2:216173455 T 471 NM_004044.6 Transcript upstream_gene_variant - - - - - - DISTANCE=3224 rs7572061 2:216173455 T CCDS2398.1 CCDS2398.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3411 rs7608331 2:216179161 C ENSESTG00000023266 ENSESTT00000059011 Transcript intron_variant - - - - - - rs7608331 2:216179161 C ENSESTG00000023266 ENSESTT00000058986 Transcript intron_variant - - - - - - rs7608331 2:216179161 C ENSESTG00000023266 ENSESTT00000059001 Transcript intron_variant - - - - - - rs7608331 2:216179161 C ENSESTG00000023266 ENSESTT00000058948 Transcript intron_variant - - - - - - rs7608331 2:216179161 C ENSESTG00000023266 ENSESTT00000059007 Transcript intron_variant - - - - - - rs7608331 2:216179161 C ENSESTG00000023266 ENSESTT00000058963 Transcript intron_variant - - - - - - rs7608331 2:216179161 C 471 NM_004044.6 Transcript intron_variant - - - - - - rs7608331 2:216179161 C CCDS2398.1 CCDS2398.1 Transcript intron_variant - - - - - - rs7594036 2:216199881 G ENSESTG00000023266 ENSESTT00000059011 Transcript intron_variant - - - - - - rs7594036 2:216199881 G ENSESTG00000023266 ENSESTT00000058986 Transcript intron_variant - - - - - - rs7594036 2:216199881 G ENSESTG00000023266 ENSESTT00000059001 Transcript intron_variant - - - - - - rs7594036 2:216199881 G ENSESTG00000023266 ENSESTT00000058948 Transcript intron_variant - - - - - - rs7594036 2:216199881 G ENSESTG00000023266 ENSESTT00000059007 Transcript intron_variant - - - - - - rs7594036 2:216199881 G ENSESTG00000023266 ENSESTT00000058963 Transcript intron_variant - - - - - - rs7594036 2:216199881 G 471 NM_004044.6 Transcript intron_variant - - - - - - rs7594036 2:216199881 G CCDS2398.1 CCDS2398.1 Transcript intron_variant - - - - - - rs7594036 2:216199881 G ENSESTG00000023266 ENSESTT00000059047 Transcript intron_variant - - - - - - rs7594036 2:216199881 G ENSESTG00000023266 ENSESTT00000059044 Transcript intron_variant - - - - - - rs6435901 2:216207390 G ENSESTG00000023266 ENSESTT00000059011 Transcript intron_variant - - - - - - rs6435901 2:216207390 G ENSESTG00000023266 ENSESTT00000058986 Transcript intron_variant - - - - - - rs6435901 2:216207390 G ENSESTG00000023266 ENSESTT00000059001 Transcript intron_variant - - - - - - rs6435901 2:216207390 G ENSESTG00000023266 ENSESTT00000058948 Transcript intron_variant - - - - - - rs6435901 2:216207390 G ENSESTG00000023266 ENSESTT00000059007 Transcript intron_variant - - - - - - rs6435901 2:216207390 G ENSESTG00000023266 ENSESTT00000058963 Transcript intron_variant - - - - - - rs6435901 2:216207390 G 471 NM_004044.6 Transcript intron_variant - - - - - - rs6435901 2:216207390 G CCDS2398.1 CCDS2398.1 Transcript intron_variant - - - - - - rs6435901 2:216207390 G ENSESTG00000023266 ENSESTT00000059047 Transcript intron_variant - - - - - - rs6435901 2:216207390 G ENSESTG00000023266 ENSESTT00000059044 Transcript intron_variant - - - - - - rs10932609 2:216211712 T ENSESTG00000023266 ENSESTT00000059011 Transcript downstream_gene_variant - - - - - - DISTANCE=202 rs10932609 2:216211712 T ENSESTG00000023266 ENSESTT00000058986 Transcript downstream_gene_variant - - - - - - DISTANCE=136 rs10932609 2:216211712 T ENSESTG00000023430 ENSESTT00000059086 Transcript upstream_gene_variant - - - - - - DISTANCE=2175 rs10932609 2:216211712 T ENSESTG00000023266 ENSESTT00000059001 Transcript downstream_gene_variant - - - - - - DISTANCE=136 rs10932609 2:216211712 T ENSESTG00000023266 ENSESTT00000058948 Transcript downstream_gene_variant - - - - - - DISTANCE=136 rs10932609 2:216211712 T ENSESTG00000023266 ENSESTT00000059007 Transcript downstream_gene_variant - - - - - - DISTANCE=202 rs10932609 2:216211712 T ENSESTG00000023266 ENSESTT00000058963 Transcript downstream_gene_variant - - - - - - DISTANCE=202 rs10932609 2:216211712 T 471 NM_004044.6 Transcript intron_variant - - - - - - rs10932609 2:216211712 T CCDS2398.1 CCDS2398.1 Transcript intron_variant - - - - - - rs10932609 2:216211712 T ENSESTG00000023266 ENSESTT00000059047 Transcript downstream_gene_variant - - - - - - DISTANCE=202 rs10932609 2:216211712 T ENSESTG00000023266 ENSESTT00000059044 Transcript downstream_gene_variant - - - - - - DISTANCE=136 rs4276026 2:216619902 G ENSESTG00000004138 ENSESTT00000010456 Transcript intron_variant - - - - - - rs4276026 2:216619902 G 646324 NR_037195.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4276026 2:216619902 G ENSESTG00000004138 ENSESTT00000010451 Transcript intron_variant - - - - - - rs4276026 2:216619902 G ENSESTG00000004138 ENSESTT00000010460 Transcript intron_variant - - - - - - rs4674037 2:216763850 C - ENSR00001551566 RegulatoryFeature regulatory_region_variant - - - - - - rs4674037 2:216763850 C - - - intergenic_variant - - - - - - rs2888387 2:216926471 T CCDS33375.1 CCDS33375.1 Transcript intron_variant - - - - - - rs2888387 2:216926471 T 55825 NM_018441.5 Transcript intron_variant - - - - - - rs2888387 2:216926471 T ENSESTG00000004118 ENSESTT00000010397 Transcript intron_variant - - - - - - rs284533 2:217330910 G ENSESTG00000007289 ENSESTT00000018471 Transcript intron_variant - - - - - - rs284533 2:217330910 G 50485 NM_014140.3 Transcript intron_variant - - - - - - rs284533 2:217330910 G 50485 NM_001127207.1 Transcript intron_variant - - - - - - rs284533 2:217330910 G ENSESTG00000007289 ENSESTT00000018463 Transcript intron_variant - - - - - - rs284533 2:217330910 G CCDS2403.1 CCDS2403.1 Transcript intron_variant - - - - - - rs1554714 2:217428203 G - ENSR00000607273 RegulatoryFeature regulatory_region_variant - - - - - - rs1554714 2:217428203 G - - - intergenic_variant - - - - - - rs1864443 2:218032951 G - - - intergenic_variant - - - - - - rs2216947 2:218136234 A ENSESTG00000007397 ENSESTT00000018611 Transcript intron_variant - - - - - - rs934041 2:218821530 G ENSESTG00000033662 ENSESTT00000085114 Transcript intron_variant - - - - - - rs934041 2:218821530 G ENSESTG00000033662 ENSESTT00000085125 Transcript intron_variant - - - - - - rs2059740 2:218892975 C - - - intergenic_variant - - - - - - rs3113997 2:219837250 C 151300 NR_015390.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3756 rs3113997 2:219837250 C 151300 NR_024385.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3756 rs907679 2:220250147 G ENSESTG00000030157 ENSESTT00000076314 Transcript intron_variant - - - - - - rs907679 2:220250147 G ENSESTG00000030157 ENSESTT00000076280 Transcript missense_variant,splice_region_variant 907 773 258 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs907679 2:220250147 G ENSESTG00000030157 ENSESTT00000076259 Transcript missense_variant,splice_region_variant 879 797 266 V/A gTg/gCg - rs907679 2:220250147 G 23549 NM_012100.2 Transcript missense_variant,splice_region_variant 919 773 258 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs907679 2:220250147 G CCDS42823.1 CCDS42823.1 Transcript missense_variant,splice_region_variant 773 773 258 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs907679 2:220250147 G ENSESTG00000030157 ENSESTT00000076299 Transcript missense_variant,splice_region_variant 907 773 258 V/A gTg/gCg - rs907679 2:220250147 G ENSESTG00000030157 ENSESTT00000076245 Transcript missense_variant,splice_region_variant 879 797 266 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs907679 2:220250147 G ENSESTG00000030157 ENSESTT00000076211 Transcript missense_variant,splice_region_variant 777 614 205 V/A gTg/gCg - rs907679 2:220250147 G ENSESTG00000030157 ENSESTT00000076186 Transcript missense_variant,splice_region_variant 777 614 205 V/A gTg/gCg - rs907679 2:220250147 G ENSESTG00000030157 ENSESTT00000076378 Transcript upstream_gene_variant - - - - - - DISTANCE=852 rs907679 2:220250147 G ENSESTG00000030157 ENSESTT00000076353 Transcript intron_variant - - - - - - rs907679 2:220250147 G ENSESTG00000030138 ENSESTT00000075856 Transcript intron_variant - - - - - - rs10804279 2:220603237 C ENSESTG00000009040 ENSESTT00000022699 Transcript downstream_gene_variant - - - - - - DISTANCE=594 rs2971632 2:220900715 A - - - intergenic_variant - - - - - - rs4627551 2:221843713 C - - - intergenic_variant - - - - - - rs6746048 2:222088398 C - - - intergenic_variant - - - - - - rs1975129 2:222130306 A - - - intergenic_variant - - - - - - rs7606143 2:222151046 T - - - intergenic_variant - - - - - - rs6738030 2:222160311 A - - - intergenic_variant - - - - - - rs1246297 2:222187778 T - - - intergenic_variant - - - - - - rs348972 2:222920490 G - - - intergenic_variant - - - - - - rs4375856 2:223310569 C CCDS2453.1 CCDS2453.1 Transcript intron_variant - - - - - - rs4375856 2:223310569 C 130367 NM_152386.2 Transcript intron_variant - - - - - - rs4375856 2:223310569 C ENSESTG00000008206 ENSESTT00000020755 Transcript intron_variant - - - - - - rs10153812 2:223641005 C - - - intergenic_variant - - - - - - rs935030 2:223799207 T 2181 NM_203372.1 Transcript intron_variant - - - - - - rs935030 2:223799207 T ENSESTG00000008249 ENSESTT00000020986 Transcript intron_variant - - - - - - rs935030 2:223799207 T ENSESTG00000008249 ENSESTT00000020955 Transcript intron_variant - - - - - - rs935030 2:223799207 T ENSESTG00000008249 ENSESTT00000020964 Transcript intron_variant - - - - - - rs935030 2:223799207 T ENSESTG00000008249 ENSESTT00000020971 Transcript intron_variant - - - - - - rs935030 2:223799207 T ENSESTG00000008249 ENSESTT00000020981 Transcript intron_variant - - - - - - rs935030 2:223799207 T 2181 NM_004457.3 Transcript intron_variant - - - - - - rs935030 2:223799207 T CCDS2455.1 CCDS2455.1 Transcript intron_variant - - - - - - rs935030 2:223799207 T ENSESTG00000008249 ENSESTT00000020950 Transcript intron_variant - - - - - - rs7582553 2:223930377 G - - - intergenic_variant - - - - - - rs2121948 2:224059183 G - - - intergenic_variant - - - - - - rs6718320 2:224359061 C ENSESTG00000034003 ENSESTT00000085952 Transcript upstream_gene_variant - - - - - - DISTANCE=3079 rs1250904 2:224452893 C - - - intergenic_variant - - - - - - rs7598343 2:224483166 C - ENSR00000608295 RegulatoryFeature regulatory_region_variant - - - - - - rs7598343 2:224483166 C - - - intergenic_variant - - - - - - rs1250814 2:224728598 G ENSESTG00000034063 ENSESTT00000086099 Transcript intron_variant - - - - - - rs562853 2:224779980 G ENSESTG00000034048 ENSESTT00000086072 Transcript intron_variant - - - - - - rs562853 2:224779980 G CCDS33387.1 CCDS33387.1 Transcript intron_variant - - - - - - rs562853 2:224779980 G 57590 NM_020830.3 Transcript intron_variant - - - - - - rs562853 2:224779980 G ENSESTG00000034048 ENSESTT00000086076 Transcript intron_variant - - - - - - rs542343 2:224783655 C - ENSR00000608355 RegulatoryFeature regulatory_region_variant - - - - - - rs542343 2:224783655 C ENSESTG00000034048 ENSESTT00000086072 Transcript intron_variant - - - - - - rs542343 2:224783655 C CCDS33387.1 CCDS33387.1 Transcript intron_variant - - - - - - rs542343 2:224783655 C 57590 NM_020830.3 Transcript intron_variant - - - - - - rs542343 2:224783655 C ENSESTG00000034048 ENSESTT00000086076 Transcript intron_variant - - - - - - rs6707243 2:224831891 A CCDS2459.1 CCDS2459.1 Transcript downstream_gene_variant - - - - - - DISTANCE=140 rs6707243 2:224831891 A 65080 NM_022915.3 Transcript 3_prime_UTR_variant 1208 - - - - - rs6707243 2:224831891 A ENSESTG00000034012 ENSESTT00000085991 Transcript 3_prime_UTR_variant 1202 - - - - - rs4674834 2:224853780 C CCDS46526.1 CCDS46526.1 Transcript intron_variant - - - - - - rs4674834 2:224853780 C 5270 NM_006216.3 Transcript intron_variant - - - - - - rs4674834 2:224853780 C 5270 NM_001136530.1 Transcript intron_variant - - - - - - rs4674834 2:224853780 C CCDS46525.1 CCDS46525.1 Transcript intron_variant - - - - - - rs4674834 2:224853780 C 5270 NM_001136528.1 Transcript intron_variant - - - - - - rs4674834 2:224853780 C CCDS2460.1 CCDS2460.1 Transcript intron_variant - - - - - - rs9288587 2:225142457 C - - - intergenic_variant - - - - - - rs2245983 2:225228221 C - - - intergenic_variant - - - - - - rs1449061 2:226001778 C - - - intergenic_variant - - - - - - rs7574299 2:226422573 A 57624 NM_020864.1 Transcript intron_variant - - - - - - rs7574299 2:226422573 A CCDS46529.1 CCDS46529.1 Transcript intron_variant - - - - - - rs7574299 2:226422573 A ENSESTG00000017816 ENSESTT00000044875 Transcript intron_variant - - - - - - rs2860247 2:227096342 G - - - intergenic_variant - - - - - - rs6706812 2:227848865 C ENSESTG00000009657 ENSESTT00000024207 Transcript intron_variant - - - - - - rs6706812 2:227848865 C CCDS2464.1 CCDS2464.1 Transcript intron_variant - - - - - - rs6706812 2:227848865 C ENSESTG00000009657 ENSESTT00000024203 Transcript intron_variant - - - - - - rs6706812 2:227848865 C 84236 NM_032276.3 Transcript intron_variant - - - - - - rs6706812 2:227848865 C ENSESTG00000009657 ENSESTT00000024198 Transcript intron_variant - - - - - - rs6706812 2:227848865 C 84236 NM_001167608.1 Transcript intron_variant - - - - - - rs6436675 2:228159063 C ENSESTG00000009688 ENSESTT00000024285 Transcript downstream_gene_variant - - - - - - DISTANCE=3384 rs6436675 2:228159063 C ENSESTG00000009688 ENSESTT00000024274 Transcript intron_variant - - - - - - rs6436675 2:228159063 C ENSESTG00000009790 ENSESTT00000024521 Transcript intron_variant - - - - - - rs6436675 2:228159063 C ENSESTG00000009688 ENSESTT00000024297 Transcript upstream_gene_variant - - - - - - DISTANCE=1952 rs6436675 2:228159063 C ENSESTG00000009790 ENSESTT00000024492 Transcript intron_variant - - - - - - rs6436675 2:228159063 C ENSESTG00000009688 ENSESTT00000024281 Transcript 3_prime_UTR_variant 1131 - - - - - rs6436675 2:228159063 C CCDS42829.1 CCDS42829.1 Transcript intron_variant - - - - - - rs6436675 2:228159063 C ENSESTG00000009790 ENSESTT00000024506 Transcript intron_variant - - - - - - rs6436675 2:228159063 C ENSESTG00000009790 ENSESTT00000024511 Transcript intron_variant - - - - - - rs6436675 2:228159063 C 1285 NM_000091.4 Transcript intron_variant - - - - - - rs7572710 2:228160786 G - ENSR00001552598 RegulatoryFeature regulatory_region_variant - - - - - - rs7572710 2:228160786 G ENSESTG00000009688 ENSESTT00000024274 Transcript intron_variant - - - - - - rs7572710 2:228160786 G ENSESTG00000009790 ENSESTT00000024521 Transcript intron_variant - - - - - - rs7572710 2:228160786 G ENSESTG00000009688 ENSESTT00000024297 Transcript upstream_gene_variant - - - - - - DISTANCE=229 rs7572710 2:228160786 G ENSESTG00000009790 ENSESTT00000024492 Transcript intron_variant - - - - - - rs7572710 2:228160786 G ENSESTG00000009688 ENSESTT00000024281 Transcript downstream_gene_variant - - - - - - DISTANCE=1081 rs7572710 2:228160786 G CCDS42829.1 CCDS42829.1 Transcript intron_variant - - - - - - rs7572710 2:228160786 G ENSESTG00000009790 ENSESTT00000024506 Transcript intron_variant - - - - - - rs7572710 2:228160786 G ENSESTG00000009790 ENSESTT00000024511 Transcript intron_variant - - - - - - rs7572710 2:228160786 G 1285 NM_000091.4 Transcript intron_variant - - - - - - rs4436947 2:228173078 G ENSESTG00000009790 ENSESTT00000024521 Transcript intron_variant - - - - - - rs4436947 2:228173078 G ENSESTG00000009704 ENSESTT00000024310 Transcript intron_variant - - - - - - rs4436947 2:228173078 G ENSESTG00000009688 ENSESTT00000024297 Transcript downstream_gene_variant - - - - - - DISTANCE=4034 rs4436947 2:228173078 G ENSESTG00000009790 ENSESTT00000024492 Transcript intron_variant - - - - - - rs4436947 2:228173078 G CCDS42829.1 CCDS42829.1 Transcript intron_variant - - - - - - rs4436947 2:228173078 G ENSESTG00000009790 ENSESTT00000024506 Transcript intron_variant - - - - - - rs4436947 2:228173078 G ENSESTG00000009790 ENSESTT00000024511 Transcript intron_variant - - - - - - rs4436947 2:228173078 G 1285 NM_000091.4 Transcript intron_variant - - - - - - rs7567291 2:228178780 C ENSESTG00000009790 ENSESTT00000024492 Transcript intron_variant - - - - - - rs7567291 2:228178780 C CCDS42829.1 CCDS42829.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2194 rs7567291 2:228178780 C ENSESTG00000009790 ENSESTT00000024521 Transcript intron_variant - - - - - - rs7567291 2:228178780 C ENSESTG00000009790 ENSESTT00000024511 Transcript intron_variant - - - - - - rs7567291 2:228178780 C ENSESTG00000009790 ENSESTT00000024506 Transcript intron_variant - - - - - - rs7567291 2:228178780 C ENSESTG00000009704 ENSESTT00000024310 Transcript downstream_gene_variant - - - - - - DISTANCE=1969 rs7567291 2:228178780 C 1285 NM_000091.4 Transcript 3_prime_UTR_variant 7369 - - - - - rs12694726 2:228185428 G ENSESTG00000009726 ENSESTT00000024423 Transcript upstream_gene_variant - - - - - - DISTANCE=4736 rs12694726 2:228185428 G ENSESTG00000009790 ENSESTT00000024521 Transcript intron_variant - - - - - - rs12694726 2:228185428 G ENSESTG00000009726 ENSESTT00000024415 Transcript upstream_gene_variant - - - - - - DISTANCE=4653 rs12694726 2:228185428 G ENSESTG00000009726 ENSESTT00000024404 Transcript upstream_gene_variant - - - - - - DISTANCE=4580 rs12694726 2:228185428 G ENSESTG00000009726 ENSESTT00000024425 Transcript upstream_gene_variant - - - - - - DISTANCE=4736 rs12694726 2:228185428 G ENSESTG00000009790 ENSESTT00000024492 Transcript intron_variant - - - - - - rs12694726 2:228185428 G ENSESTG00000009726 ENSESTT00000024407 Transcript upstream_gene_variant - - - - - - DISTANCE=4580 rs12694726 2:228185428 G ENSESTG00000009726 ENSESTT00000024416 Transcript upstream_gene_variant - - - - - - DISTANCE=4653 rs12694726 2:228185428 G ENSESTG00000009726 ENSESTT00000024356 Transcript upstream_gene_variant - - - - - - DISTANCE=4579 rs12694726 2:228185428 G ENSESTG00000009726 ENSESTT00000024419 Transcript upstream_gene_variant - - - - - - DISTANCE=4736 rs12694726 2:228185428 G ENSESTG00000009790 ENSESTT00000024506 Transcript intron_variant - - - - - - rs12694726 2:228185428 G ENSESTG00000009790 ENSESTT00000024511 Transcript intron_variant - - - - - - rs6741297 2:228199047 C 56947 NM_020194.4 Transcript intron_variant - - - - - - rs6741297 2:228199047 C ENSESTG00000009726 ENSESTT00000024423 Transcript intron_variant - - - - - - rs6741297 2:228199047 C ENSESTG00000009726 ENSESTT00000024415 Transcript intron_variant - - - - - - rs6741297 2:228199047 C ENSESTG00000009726 ENSESTT00000024404 Transcript intron_variant - - - - - - rs6741297 2:228199047 C CCDS2465.1 CCDS2465.1 Transcript intron_variant - - - - - - rs6741297 2:228199047 C ENSESTG00000009726 ENSESTT00000024407 Transcript intron_variant - - - - - - rs6741297 2:228199047 C ENSESTG00000009726 ENSESTT00000024425 Transcript intron_variant - - - - - - rs6741297 2:228199047 C ENSESTG00000009726 ENSESTT00000024356 Transcript intron_variant - - - - - - rs6741297 2:228199047 C ENSESTG00000009726 ENSESTT00000024416 Transcript intron_variant - - - - - - rs6741297 2:228199047 C ENSESTG00000009726 ENSESTT00000024419 Transcript intron_variant - - - - - - rs10933178 2:228202305 G 56947 NM_020194.4 Transcript intron_variant - - - - - - rs10933178 2:228202305 G ENSESTG00000009726 ENSESTT00000024430 Transcript upstream_gene_variant - - - - - - DISTANCE=2771 rs10933178 2:228202305 G ENSESTG00000009726 ENSESTT00000024423 Transcript intron_variant - - - - - - rs10933178 2:228202305 G ENSESTG00000009726 ENSESTT00000024415 Transcript intron_variant - - - - - - rs10933178 2:228202305 G ENSESTG00000009726 ENSESTT00000024404 Transcript intron_variant - - - - - - rs10933178 2:228202305 G CCDS2465.1 CCDS2465.1 Transcript intron_variant - - - - - - rs10933178 2:228202305 G ENSESTG00000009726 ENSESTT00000024407 Transcript intron_variant - - - - - - rs10933178 2:228202305 G ENSESTG00000009726 ENSESTT00000024425 Transcript intron_variant - - - - - - rs10933178 2:228202305 G ENSESTG00000009726 ENSESTT00000024356 Transcript intron_variant - - - - - - rs10933178 2:228202305 G ENSESTG00000009726 ENSESTT00000024416 Transcript intron_variant - - - - - - rs10933178 2:228202305 G ENSESTG00000009726 ENSESTT00000024419 Transcript intron_variant - - - - - - rs4396711 2:228206970 A 56947 NM_020194.4 Transcript intron_variant - - - - - - rs4396711 2:228206970 A ENSESTG00000009726 ENSESTT00000024430 Transcript intron_variant - - - - - - rs4396711 2:228206970 A ENSESTG00000009726 ENSESTT00000024423 Transcript intron_variant - - - - - - rs4396711 2:228206970 A ENSESTG00000009726 ENSESTT00000024415 Transcript intron_variant - - - - - - rs4396711 2:228206970 A ENSESTG00000009726 ENSESTT00000024404 Transcript intron_variant - - - - - - rs4396711 2:228206970 A CCDS2465.1 CCDS2465.1 Transcript intron_variant - - - - - - rs4396711 2:228206970 A ENSESTG00000009726 ENSESTT00000024407 Transcript intron_variant - - - - - - rs4396711 2:228206970 A ENSESTG00000009726 ENSESTT00000024425 Transcript intron_variant - - - - - - rs4396711 2:228206970 A ENSESTG00000009726 ENSESTT00000024356 Transcript intron_variant - - - - - - rs4396711 2:228206970 A ENSESTG00000009726 ENSESTT00000024416 Transcript intron_variant - - - - - - rs4396711 2:228206970 A ENSESTG00000009726 ENSESTT00000024419 Transcript intron_variant - - - - - - rs9678000 2:228237313 C ENSESTG00000009769 ENSESTT00000024461 Transcript intron_variant - - - - - - rs9678000 2:228237313 C CCDS2466.1 CCDS2466.1 Transcript intron_variant - - - - - - rs9678000 2:228237313 C 79853 NM_024795.3 Transcript intron_variant - - - - - - rs4575714 2:228303768 C - - - intergenic_variant - - - - - - rs6436697 2:228329377 G - - - intergenic_variant - - - - - - rs6436699 2:228360861 C ENSESTG00000017268 ENSESTT00000043513 Transcript intron_variant - - - - - - rs6436699 2:228360861 C 3267 NM_001135188.1 Transcript intron_variant - - - - - - rs6436699 2:228360861 C 3267 NM_001135189.1 Transcript intron_variant - - - - - - rs6436699 2:228360861 C CCDS46535.1 CCDS46535.1 Transcript intron_variant - - - - - - rs6436699 2:228360861 C CCDS2467.1 CCDS2467.1 Transcript intron_variant - - - - - - rs6436699 2:228360861 C CCDS46533.1 CCDS46533.1 Transcript intron_variant - - - - - - rs6436699 2:228360861 C CCDS46534.1 CCDS46534.1 Transcript intron_variant - - - - - - rs6436699 2:228360861 C 3267 NM_001135187.1 Transcript intron_variant - - - - - - rs6436699 2:228360861 C 3267 NM_004504.4 Transcript intron_variant - - - - - - rs6436699 2:228360861 C ENSESTG00000017268 ENSESTT00000043497 Transcript intron_variant - - - - - - rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043519 Transcript upstream_gene_variant - - - - - - DISTANCE=2188 rs4358114 2:228370800 C 3267 NM_001135188.1 Transcript intron_variant - - - - - - rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043537 Transcript upstream_gene_variant - - - - - - DISTANCE=4637 rs4358114 2:228370800 C CCDS46533.1 CCDS46533.1 Transcript intron_variant - - - - - - rs4358114 2:228370800 C 3267 NM_004504.4 Transcript intron_variant - - - - - - rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043497 Transcript intron_variant - - - - - - rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043513 Transcript intron_variant - - - - - - rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043543 Transcript upstream_gene_variant - - - - - - DISTANCE=4637 rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043516 Transcript upstream_gene_variant - - - - - - DISTANCE=2188 rs4358114 2:228370800 C 3267 NM_001135189.1 Transcript intron_variant - - - - - - rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043552 Transcript upstream_gene_variant - - - - - - DISTANCE=4637 rs4358114 2:228370800 C CCDS46535.1 CCDS46535.1 Transcript intron_variant - - - - - - rs4358114 2:228370800 C CCDS2467.1 CCDS2467.1 Transcript intron_variant - - - - - - rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043554 Transcript upstream_gene_variant - - - - - - DISTANCE=4637 rs4358114 2:228370800 C CCDS46534.1 CCDS46534.1 Transcript intron_variant - - - - - - rs4358114 2:228370800 C 3267 NM_001135187.1 Transcript intron_variant - - - - - - rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043524 Transcript upstream_gene_variant - - - - - - DISTANCE=2188 rs4358114 2:228370800 C ENSESTG00000017268 ENSESTT00000043565 Transcript upstream_gene_variant - - - - - - DISTANCE=4637 rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043519 Transcript intron_variant - - - - - - rs11691863 2:228375608 T 3267 NM_001135188.1 Transcript intron_variant - - - - - - rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043537 Transcript intron_variant - - - - - - rs11691863 2:228375608 T CCDS46533.1 CCDS46533.1 Transcript intron_variant - - - - - - rs11691863 2:228375608 T 3267 NM_004504.4 Transcript intron_variant - - - - - - rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043497 Transcript intron_variant - - - - - - rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043513 Transcript intron_variant - - - - - - rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043543 Transcript intron_variant - - - - - - rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043516 Transcript intron_variant - - - - - - rs11691863 2:228375608 T 3267 NM_001135189.1 Transcript intron_variant - - - - - - rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043552 Transcript intron_variant - - - - - - rs11691863 2:228375608 T CCDS46535.1 CCDS46535.1 Transcript intron_variant - - - - - - rs11691863 2:228375608 T CCDS2467.1 CCDS2467.1 Transcript intron_variant - - - - - - rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043554 Transcript intron_variant - - - - - - rs11691863 2:228375608 T CCDS46534.1 CCDS46534.1 Transcript intron_variant - - - - - - rs11691863 2:228375608 T 3267 NM_001135187.1 Transcript intron_variant - - - - - - rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043524 Transcript intron_variant - - - - - - rs11691863 2:228375608 T ENSESTG00000017268 ENSESTT00000043565 Transcript intron_variant - - - - - - rs12053112 2:228395648 A ENSESTG00000017268 ENSESTT00000043519 Transcript intron_variant - - - - - - rs12053112 2:228395648 A 3267 NM_001135188.1 Transcript intron_variant - - - - - - rs12053112 2:228395648 A ENSESTG00000017268 ENSESTT00000043537 Transcript intron_variant - - - - - - rs12053112 2:228395648 A CCDS46533.1 CCDS46533.1 Transcript intron_variant - - - - - - rs12053112 2:228395648 A 3267 NM_004504.4 Transcript intron_variant - - - - - - rs12053112 2:228395648 A ENSESTG00000017268 ENSESTT00000043497 Transcript intron_variant - - - - - - rs12053112 2:228395648 A ENSESTG00000017268 ENSESTT00000043513 Transcript intron_variant - - - - - - rs12053112 2:228395648 A ENSESTG00000017268 ENSESTT00000043543 Transcript intron_variant - - - - - - rs12053112 2:228395648 A ENSESTG00000017268 ENSESTT00000043516 Transcript intron_variant - - - - - - rs12053112 2:228395648 A 3267 NM_001135189.1 Transcript intron_variant - - - - - - rs12053112 2:228395648 A ENSESTG00000017268 ENSESTT00000043552 Transcript intron_variant - - - - - - rs12053112 2:228395648 A CCDS46535.1 CCDS46535.1 Transcript intron_variant - - - - - - rs12053112 2:228395648 A CCDS2467.1 CCDS2467.1 Transcript intron_variant - - - - - - rs12053112 2:228395648 A ENSESTG00000017268 ENSESTT00000043554 Transcript intron_variant - - - - - - rs12053112 2:228395648 A 3267 NM_001135187.1 Transcript intron_variant - - - - - - rs12053112 2:228395648 A ENSESTG00000017268 ENSESTT00000043524 Transcript intron_variant - - - - - - rs12053112 2:228395648 A CCDS46534.1 CCDS46534.1 Transcript intron_variant - - - - - - rs10189860 2:228436716 G - - - intergenic_variant - - - - - - rs11683170 2:228460352 G - - - intergenic_variant - - - - - - rs1467181 2:228462238 T - - - intergenic_variant - - - - - - rs6718689 2:228489164 C CCDS54434.1 CCDS54434.1 Transcript intron_variant - - - - - - rs6718689 2:228489164 C 56918 NM_020161.3 Transcript intron_variant - - - - - - rs6718689 2:228489164 C CCDS33388.1 CCDS33388.1 Transcript intron_variant - - - - - - rs6718689 2:228489164 C 56918 NM_001162483.1 Transcript intron_variant - - - - - - rs10933199 2:228500131 G CCDS54434.1 CCDS54434.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2330 rs10933199 2:228500131 G 56918 NM_020161.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2095 rs10933199 2:228500131 G CCDS33388.1 CCDS33388.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2330 rs10933199 2:228500131 G 56918 NM_001162483.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2095 rs10933201 2:228523237 G - ENSR00000608847 RegulatoryFeature regulatory_region_variant - - - - - - rs10933201 2:228523237 G - - - intergenic_variant - - - - - - rs6436731 2:228591938 A - - - intergenic_variant - - - - - - rs12988955 2:228594851 A - - - intergenic_variant - - - - - - rs10167448 2:228604532 C - - - intergenic_variant - - - - - - rs10207284 2:228610969 G - - - intergenic_variant - - - - - - rs4246645 2:228658062 G - - - intergenic_variant - - - - - - rs6723539 2:228675537 C ENSESTG00000017333 ENSESTT00000043624 Transcript upstream_gene_variant - - - - - - DISTANCE=3052 rs6723539 2:228675537 C CCDS46536.1 CCDS46536.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3091 rs6723539 2:228675537 C 6364 NM_004591.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3021 rs6723539 2:228675537 C 6364 NM_001130046.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3021 rs6723539 2:228675537 C CCDS2469.1 CCDS2469.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3091 rs6723539 2:228675537 C ENSESTG00000017333 ENSESTT00000043616 Transcript upstream_gene_variant - - - - - - DISTANCE=3033 rs4973359 2:228692034 C - - - intergenic_variant - - - - - - rs7577621 2:228697479 A - - - intergenic_variant - - - - - - rs6735420 2:228699411 C - ENSR00000608879 RegulatoryFeature regulatory_region_variant - - - - - - rs6735420 2:228699411 C - - - intergenic_variant - - - - - - rs10211109 2:228707545 A - - - intergenic_variant - - - - - - rs6733893 2:228713097 A - - - intergenic_variant - - - - - - rs7593794 2:228721187 C - - - intergenic_variant - - - - - - rs1721365 2:228812684 A - - - intergenic_variant - - - - - - rs1715831 2:228825612 C - - - intergenic_variant - - - - - - rs1721351 2:228826851 T - - - intergenic_variant - - - - - - rs4531922 2:228921340 T CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs4531922 2:228921340 T CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs4531922 2:228921340 T 80309 NM_030623.3 Transcript intron_variant - - - - - - rs4531922 2:228921340 T 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs4531922 2:228921340 T ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs4340503 2:228928099 C CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs4340503 2:228928099 C CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs4340503 2:228928099 C 80309 NM_030623.3 Transcript intron_variant - - - - - - rs4340503 2:228928099 C 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs4340503 2:228928099 C ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs6755054 2:228933380 C CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs6755054 2:228933380 C CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs6755054 2:228933380 C 80309 NM_030623.3 Transcript intron_variant - - - - - - rs6755054 2:228933380 C 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs6755054 2:228933380 C ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs4594430 2:228952452 T CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs4594430 2:228952452 T CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs4594430 2:228952452 T 80309 NM_030623.3 Transcript intron_variant - - - - - - rs4594430 2:228952452 T 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs4594430 2:228952452 T ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs4640377 2:228956521 T CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs4640377 2:228956521 T CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs4640377 2:228956521 T 80309 NM_030623.3 Transcript intron_variant - - - - - - rs4640377 2:228956521 T 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs4640377 2:228956521 T ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs7589603 2:228959592 C CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs7589603 2:228959592 C CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs7589603 2:228959592 C 80309 NM_030623.3 Transcript intron_variant - - - - - - rs7589603 2:228959592 C 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs7589603 2:228959592 C ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs6436751 2:228965469 G CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs6436751 2:228965469 G CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs6436751 2:228965469 G 80309 NM_030623.3 Transcript intron_variant - - - - - - rs6436751 2:228965469 G 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs6436751 2:228965469 G ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs6436752 2:228989695 G CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs6436752 2:228989695 G CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs6436752 2:228989695 G 80309 NM_030623.3 Transcript intron_variant - - - - - - rs6436752 2:228989695 G 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs6436752 2:228989695 G ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs4364016 2:228991314 C CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs4364016 2:228991314 C CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs4364016 2:228991314 C 80309 NM_030623.3 Transcript intron_variant - - - - - - rs4364016 2:228991314 C 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs4364016 2:228991314 C ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs6436759 2:229013819 G CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs6436759 2:229013819 G CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs6436759 2:229013819 G 80309 NM_030623.3 Transcript intron_variant - - - - - - rs6436759 2:229013819 G 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs6436759 2:229013819 G ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs10933241 2:229030133 A CCDS46537.1 CCDS46537.1 Transcript intron_variant - - - - - - rs10933241 2:229030133 A CCDS33389.1 CCDS33389.1 Transcript intron_variant - - - - - - rs10933241 2:229030133 A 80309 NM_030623.3 Transcript intron_variant - - - - - - rs10933241 2:229030133 A 80309 NM_001142644.1 Transcript intron_variant - - - - - - rs10933241 2:229030133 A ENSESTG00000017410 ENSESTT00000043811 Transcript intron_variant - - - - - - rs6718972 2:229093591 A - - - intergenic_variant - - - - - - rs4144813 2:229126727 A - - - intergenic_variant - - - - - - rs1918895 2:229145491 A - - - intergenic_variant - - - - - - rs1358465 2:229160842 A - - - intergenic_variant - - - - - - rs1358467 2:229162097 T - - - intergenic_variant - - - - - - rs1973840 2:229192538 G - - - intergenic_variant - - - - - - rs1406140 2:229201884 G - - - intergenic_variant - - - - - - rs6709300 2:229215670 A - - - intergenic_variant - - - - - - rs8179759 2:229231430 G - - - intergenic_variant - - - - - - rs2164407 2:229461860 A - - - intergenic_variant - - - - - - rs6712197 2:229469816 G - - - intergenic_variant - - - - - - rs808989 2:229642949 T - ENSR00001552673 RegulatoryFeature regulatory_region_variant - - - - - - rs808989 2:229642949 T - - - intergenic_variant - - - - - - rs1728358 2:229650446 G - - - intergenic_variant - - - - - - rs776979 2:229666454 A - - - intergenic_variant - - - - - - rs1527665 2:229670517 T - - - intergenic_variant - - - - - - rs1727567 2:229672248 G - - - intergenic_variant - - - - - - rs6761886 2:229673970 G - - - intergenic_variant - - - - - - rs1609185 2:229681206 T - - - intergenic_variant - - - - - - rs6760494 2:229686026 T - - - intergenic_variant - - - - - - rs2894663 2:229695360 C - - - intergenic_variant - - - - - - rs4510215 2:229717685 T - - - intergenic_variant - - - - - - rs1918469 2:229721685 G - - - intergenic_variant - - - - - - rs800740 2:229734464 A - ENSR00000608936 RegulatoryFeature regulatory_region_variant - - - - - - rs800740 2:229734464 A - - - intergenic_variant - - - - - - rs31274 2:229900828 G 55022 NM_017933.4 Transcript intron_variant - - - - - - rs31274 2:229900828 G ENSESTG00000014517 ENSESTT00000036371 Transcript intron_variant - - - - - - rs31274 2:229900828 G 55022 NM_001100818.1 Transcript intron_variant - - - - - - rs31274 2:229900828 G CCDS42830.1 CCDS42830.1 Transcript intron_variant - - - - - - rs31274 2:229900828 G CCDS2471.1 CCDS2471.1 Transcript intron_variant - - - - - - rs2765935 2:229930886 G 55022 NM_017933.4 Transcript intron_variant - - - - - - rs2765935 2:229930886 G ENSESTG00000014517 ENSESTT00000036371 Transcript intron_variant - - - - - - rs2765935 2:229930886 G 55022 NM_001100818.1 Transcript intron_variant - - - - - - rs2765935 2:229930886 G CCDS42830.1 CCDS42830.1 Transcript intron_variant - - - - - - rs2765935 2:229930886 G CCDS2471.1 CCDS2471.1 Transcript intron_variant - - - - - - rs2894670 2:229934660 G 55022 NM_017933.4 Transcript intron_variant - - - - - - rs2894670 2:229934660 G ENSESTG00000014517 ENSESTT00000036371 Transcript intron_variant - - - - - - rs2894670 2:229934660 G 55022 NM_001100818.1 Transcript intron_variant - - - - - - rs2894670 2:229934660 G CCDS42830.1 CCDS42830.1 Transcript intron_variant - - - - - - rs2894670 2:229934660 G CCDS2471.1 CCDS2471.1 Transcript intron_variant - - - - - - rs917730 2:229947824 G 55022 NM_017933.4 Transcript intron_variant - - - - - - rs917730 2:229947824 G ENSESTG00000014517 ENSESTT00000036371 Transcript intron_variant - - - - - - rs917730 2:229947824 G 55022 NM_001100818.1 Transcript intron_variant - - - - - - rs917730 2:229947824 G CCDS42830.1 CCDS42830.1 Transcript intron_variant - - - - - - rs917730 2:229947824 G CCDS2471.1 CCDS2471.1 Transcript intron_variant - - - - - - rs1017116 2:229961061 T 55022 NM_017933.4 Transcript intron_variant - - - - - - rs1017116 2:229961061 T ENSESTG00000014517 ENSESTT00000036371 Transcript intron_variant - - - - - - rs1017116 2:229961061 T 55022 NM_001100818.1 Transcript intron_variant - - - - - - rs1017116 2:229961061 T CCDS42830.1 CCDS42830.1 Transcript intron_variant - - - - - - rs1017116 2:229961061 T CCDS2471.1 CCDS2471.1 Transcript intron_variant - - - - - - rs7596653 2:229963821 C 55022 NM_017933.4 Transcript intron_variant - - - - - - rs7596653 2:229963821 C ENSESTG00000014517 ENSESTT00000036371 Transcript intron_variant - - - - - - rs7596653 2:229963821 C 55022 NM_001100818.1 Transcript intron_variant - - - - - - rs7596653 2:229963821 C CCDS42830.1 CCDS42830.1 Transcript intron_variant - - - - - - rs7596653 2:229963821 C CCDS2471.1 CCDS2471.1 Transcript intron_variant - - - - - - rs7580175 2:230017942 A 55022 NM_017933.4 Transcript intron_variant - - - - - - rs7580175 2:230017942 A ENSESTG00000014517 ENSESTT00000036371 Transcript intron_variant - - - - - - rs7580175 2:230017942 A 55022 NM_001100818.1 Transcript intron_variant - - - - - - rs7580175 2:230017942 A CCDS42830.1 CCDS42830.1 Transcript intron_variant - - - - - - rs7580175 2:230017942 A CCDS2471.1 CCDS2471.1 Transcript intron_variant - - - - - - rs1419955 2:230028820 T - ENSR00001552694 RegulatoryFeature regulatory_region_variant - - - - - - rs1419955 2:230028820 T 55022 NM_017933.4 Transcript intron_variant - - - - - - rs1419955 2:230028820 T ENSESTG00000014517 ENSESTT00000036371 Transcript intron_variant - - - - - - rs1419955 2:230028820 T 55022 NM_001100818.1 Transcript intron_variant - - - - - - rs1419955 2:230028820 T CCDS42830.1 CCDS42830.1 Transcript intron_variant - - - - - - rs1419955 2:230028820 T CCDS2471.1 CCDS2471.1 Transcript intron_variant - - - - - - rs6705689 2:230076880 A 55022 NM_017933.4 Transcript intron_variant - - - - - - rs6705689 2:230076880 A ENSESTG00000014517 ENSESTT00000036371 Transcript intron_variant - - - - - - rs6705689 2:230076880 A 55022 NM_001100818.1 Transcript intron_variant - - - - - - rs6705689 2:230076880 A CCDS42830.1 CCDS42830.1 Transcript intron_variant - - - - - - rs6705689 2:230076880 A CCDS2471.1 CCDS2471.1 Transcript intron_variant - - - - - - rs887633 2:230137213 G 55022 NM_017933.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1156 rs887633 2:230137213 G ENSESTG00000014517 ENSESTT00000036371 Transcript upstream_gene_variant - - - - - - DISTANCE=1252 rs887633 2:230137213 G 55022 NM_001100818.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1156 rs887633 2:230137213 G CCDS42830.1 CCDS42830.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1454 rs1226949 2:230145186 G - - - intergenic_variant - - - - - - rs961019 2:230147261 A - - - intergenic_variant - - - - - - rs961018 2:230147353 C - - - intergenic_variant - - - - - - rs1226944 2:230150080 A - - - intergenic_variant - - - - - - rs1226942 2:230150394 C - - - intergenic_variant - - - - - - rs1226941 2:230151376 C - - - intergenic_variant - - - - - - rs1226938 2:230154178 A - - - intergenic_variant - - - - - - rs1226935 2:230156240 G - - - intergenic_variant - - - - - - rs1226978 2:230160827 T - - - intergenic_variant - - - - - - rs1226975 2:230162165 T - - - intergenic_variant - - - - - - rs1226972 2:230163258 C - - - intergenic_variant - - - - - - rs1226970 2:230163352 A - - - intergenic_variant - - - - - - rs1226967 2:230163861 T - - - intergenic_variant - - - - - - rs1226966 2:230164127 T - - - intergenic_variant - - - - - - rs1226965 2:230165001 G - - - intergenic_variant - - - - - - rs1226964 2:230167298 T - - - intergenic_variant - - - - - - rs1226963 2:230167426 C - - - intergenic_variant - - - - - - rs1226962 2:230167572 C - - - intergenic_variant - - - - - - rs1226957 2:230171050 C - - - intergenic_variant - - - - - - rs1226956 2:230171646 G - - - intergenic_variant - - - - - - rs1226955 2:230172114 A - - - intergenic_variant - - - - - - rs4973192 2:230228506 A - ENSR00000307064 RegulatoryFeature regulatory_region_variant - - - - - - rs4973192 2:230228506 A CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs4973192 2:230228506 A 92737 NM_139072.3 Transcript intron_variant - - - - - - rs7574590 2:230275428 G ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs7574590 2:230275428 G CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs7574590 2:230275428 G ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs7574590 2:230275428 G ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs7574590 2:230275428 G 92737 NM_139072.3 Transcript intron_variant - - - - - - rs7574590 2:230275428 G ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs7574590 2:230275428 G ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs7574590 2:230275428 G ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs7574590 2:230275428 G ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs4973199 2:230284082 A - ENSR00001552711 RegulatoryFeature regulatory_region_variant - - - - - - rs4973199 2:230284082 A ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs4973199 2:230284082 A CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs4973199 2:230284082 A ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs4973199 2:230284082 A ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs4973199 2:230284082 A 92737 NM_139072.3 Transcript intron_variant - - - - - - rs4973199 2:230284082 A ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs4973199 2:230284082 A ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs4973199 2:230284082 A ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs4973199 2:230284082 A ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs6749306 2:230289857 C ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs6749306 2:230289857 C CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs6749306 2:230289857 C ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs6749306 2:230289857 C ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs6749306 2:230289857 C 92737 NM_139072.3 Transcript intron_variant - - - - - - rs6749306 2:230289857 C ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs6749306 2:230289857 C ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs6749306 2:230289857 C ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs6749306 2:230289857 C ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs4973200 2:230291731 C ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs4973200 2:230291731 C CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs4973200 2:230291731 C ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs4973200 2:230291731 C ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs4973200 2:230291731 C 92737 NM_139072.3 Transcript intron_variant - - - - - - rs4973200 2:230291731 C ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs4973200 2:230291731 C ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs4973200 2:230291731 C ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs4973200 2:230291731 C ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs4973201 2:230292865 A ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs4973201 2:230292865 A CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs4973201 2:230292865 A ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs4973201 2:230292865 A ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs4973201 2:230292865 A 92737 NM_139072.3 Transcript intron_variant - - - - - - rs4973201 2:230292865 A ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs4973201 2:230292865 A ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs4973201 2:230292865 A ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs4973201 2:230292865 A ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs6757904 2:230294149 G ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs6757904 2:230294149 G CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs6757904 2:230294149 G ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs6757904 2:230294149 G ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs6757904 2:230294149 G 92737 NM_139072.3 Transcript intron_variant - - - - - - rs6757904 2:230294149 G ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs6757904 2:230294149 G ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs6757904 2:230294149 G ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs6757904 2:230294149 G ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs10933296 2:230308284 T ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs10933296 2:230308284 T CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs10933296 2:230308284 T ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs10933296 2:230308284 T ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs10933296 2:230308284 T 92737 NM_139072.3 Transcript intron_variant - - - - - - rs10933296 2:230308284 T ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs10933296 2:230308284 T ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs10933296 2:230308284 T ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs10933296 2:230308284 T ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs720915 2:230318413 G ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs720915 2:230318413 G CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs720915 2:230318413 G ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs720915 2:230318413 G ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs720915 2:230318413 G 92737 NM_139072.3 Transcript intron_variant - - - - - - rs720915 2:230318413 G ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs720915 2:230318413 G ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs720915 2:230318413 G ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs720915 2:230318413 G ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs7604082 2:230326771 A ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs7604082 2:230326771 A CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs7604082 2:230326771 A ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs7604082 2:230326771 A ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs7604082 2:230326771 A 92737 NM_139072.3 Transcript intron_variant - - - - - - rs7604082 2:230326771 A ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs7604082 2:230326771 A ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs7604082 2:230326771 A ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs7604082 2:230326771 A ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs2894683 2:230337905 C ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs2894683 2:230337905 C CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs2894683 2:230337905 C ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs2894683 2:230337905 C ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs2894683 2:230337905 C 92737 NM_139072.3 Transcript intron_variant - - - - - - rs2894683 2:230337905 C ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs2894683 2:230337905 C ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs2894683 2:230337905 C ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs2894683 2:230337905 C ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs977040 2:230350586 T ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs977040 2:230350586 T CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs977040 2:230350586 T ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs977040 2:230350586 T ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs977040 2:230350586 T 92737 NM_139072.3 Transcript intron_variant - - - - - - rs977040 2:230350586 T ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs977040 2:230350586 T ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs977040 2:230350586 T ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs977040 2:230350586 T ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs4972901 2:230365795 A ENSESTG00000031953 ENSESTT00000080735 Transcript intron_variant - - - - - - rs4972901 2:230365795 A CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs4972901 2:230365795 A ENSESTG00000031953 ENSESTT00000080755 Transcript intron_variant - - - - - - rs4972901 2:230365795 A ENSESTG00000031953 ENSESTT00000080722 Transcript intron_variant - - - - - - rs4972901 2:230365795 A 92737 NM_139072.3 Transcript intron_variant - - - - - - rs4972901 2:230365795 A ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs4972901 2:230365795 A ENSESTG00000031953 ENSESTT00000080747 Transcript intron_variant - - - - - - rs4972901 2:230365795 A ENSESTG00000031953 ENSESTT00000080750 Transcript intron_variant - - - - - - rs4972901 2:230365795 A ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs7607763 2:230489711 G ENSESTG00000031953 ENSESTT00000080716 Transcript intron_variant - - - - - - rs7607763 2:230489711 G CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs7607763 2:230489711 G ENSESTG00000031953 ENSESTT00000080709 Transcript intron_variant - - - - - - rs7607763 2:230489711 G ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs7607763 2:230489711 G ENSESTG00000031953 ENSESTT00000080689 Transcript intron_variant - - - - - - rs7607763 2:230489711 G 92737 NM_139072.3 Transcript intron_variant - - - - - - rs7607763 2:230489711 G ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs2193217 2:230545133 G ENSESTG00000031953 ENSESTT00000080716 Transcript intron_variant - - - - - - rs2193217 2:230545133 G CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs2193217 2:230545133 G ENSESTG00000031953 ENSESTT00000080709 Transcript intron_variant - - - - - - rs2193217 2:230545133 G ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs2193217 2:230545133 G ENSESTG00000031953 ENSESTT00000080689 Transcript intron_variant - - - - - - rs2193217 2:230545133 G 92737 NM_139072.3 Transcript intron_variant - - - - - - rs2193217 2:230545133 G ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs2253704 2:230556071 G ENSESTG00000031953 ENSESTT00000080716 Transcript intron_variant - - - - - - rs2253704 2:230556071 G CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs2253704 2:230556071 G ENSESTG00000031953 ENSESTT00000080709 Transcript intron_variant - - - - - - rs2253704 2:230556071 G ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs2253704 2:230556071 G ENSESTG00000031953 ENSESTT00000080689 Transcript intron_variant - - - - - - rs2253704 2:230556071 G 92737 NM_139072.3 Transcript intron_variant - - - - - - rs2253704 2:230556071 G ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs2193221 2:230558613 C ENSESTG00000031953 ENSESTT00000080716 Transcript intron_variant - - - - - - rs2193221 2:230558613 C CCDS33390.1 CCDS33390.1 Transcript intron_variant - - - - - - rs2193221 2:230558613 C ENSESTG00000031953 ENSESTT00000080709 Transcript intron_variant - - - - - - rs2193221 2:230558613 C ENSESTG00000031953 ENSESTT00000080683 Transcript intron_variant - - - - - - rs2193221 2:230558613 C ENSESTG00000031953 ENSESTT00000080689 Transcript intron_variant - - - - - - rs2193221 2:230558613 C 92737 NM_139072.3 Transcript intron_variant - - - - - - rs2193221 2:230558613 C ENSESTG00000031953 ENSESTT00000080703 Transcript intron_variant - - - - - - rs2033157 2:231170532 A CCDS42831.1 CCDS42831.1 Transcript intron_variant - - - - - - rs2033157 2:231170532 A ENSESTG00000031605 ENSESTT00000079758 Transcript intron_variant - - - - - - rs2033157 2:231170532 A 11262 NM_007237.4 Transcript intron_variant - - - - - - rs2033157 2:231170532 A ENSESTG00000031605 ENSESTT00000079787 Transcript intron_variant - - - - - - rs2033157 2:231170532 A ENSESTG00000031605 ENSESTT00000079772 Transcript intron_variant - - - - - - rs34068539 2:231225904 C ENSESTG00000031648 ENSESTT00000079838 Transcript intron_variant - - - - - - rs34068539 2:231225904 C 93349 NM_138402.4 Transcript intron_variant - - - - - - rs34068539 2:231225904 C ENSESTG00000031605 ENSESTT00000079758 Transcript intron_variant - - - - - - rs34068539 2:231225904 C ENSESTG00000031637 ENSESTT00000079817 Transcript intron_variant - - - - - - rs34068539 2:231225904 C CCDS46538.1 CCDS46538.1 Transcript intron_variant - - - - - - rs1678149 2:231406259 A ENSESTG00000020395 ENSESTT00000051158 Transcript downstream_gene_variant - - - - - - DISTANCE=617 rs1678149 2:231406259 A CCDS42832.1 CCDS42832.1 Transcript intron_variant - - - - - - rs1678149 2:231406259 A 6672 NM_001080391.1 Transcript intron_variant - - - - - - rs4973340 2:231511150 A - - - intergenic_variant - - - - - - rs2466151 2:231602138 A - ENSR00000307111 RegulatoryFeature regulatory_region_variant - - - - - - rs2466151 2:231602138 A ENSESTG00000020420 ENSESTT00000051332 Transcript intron_variant - - - - - - rs2466151 2:231602138 A 51719 NM_016289.3 Transcript intron_variant - - - - - - rs2466151 2:231602138 A ENSESTG00000020420 ENSESTT00000051361 Transcript intron_variant - - - - - - rs2466151 2:231602138 A 51719 NM_001130850.1 Transcript intron_variant - - - - - - rs2466151 2:231602138 A ENSESTG00000020420 ENSESTT00000051345 Transcript intron_variant - - - - - - rs2466151 2:231602138 A 51719 NM_001130849.1 Transcript intron_variant - - - - - - rs934825 2:231806301 T - - - intergenic_variant - - - - - - rs1349522 2:232110469 C - ENSR00000609249 RegulatoryFeature regulatory_region_variant - - - - - - rs1349522 2:232110469 C ENSESTG00000021156 ENSESTT00000053482 Transcript intron_variant - - - - - - rs1349522 2:232110469 C CCDS2484.1 CCDS2484.1 Transcript intron_variant - - - - - - rs1349522 2:232110469 C 80210 NM_025139.3 Transcript intron_variant - - - - - - rs1349522 2:232110469 C ENSESTG00000021156 ENSESTT00000053472 Transcript intron_variant - - - - - - rs1349522 2:232110469 C ENSESTG00000021156 ENSESTT00000053497 Transcript intron_variant - - - - - - rs1190427 2:233316429 G CCDS2492.1 CCDS2492.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4481 rs1190427 2:233316429 G ENSESTG00000003984 ENSESTT00000010089 Transcript upstream_gene_variant - - - - - - DISTANCE=4440 rs1190427 2:233316429 G 248 NM_001631.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4404 rs1190427 2:233316429 G ENSESTG00000003984 ENSESTT00000010084 Transcript upstream_gene_variant - - - - - - DISTANCE=4393 rs938568 2:233907326 G - - - intergenic_variant - - - - - - rs10933429 2:233971870 G 3635 NM_001017915.1 Transcript intron_variant - - - - - - rs10933429 2:233971870 G 3635 NM_005541.3 Transcript intron_variant - - - - - - rs10933429 2:233971870 G ENSESTG00000000056 ENSESTT00000000155 Transcript intron_variant - - - - - - rs838712 2:234287994 C ENSESTG00000008917 ENSESTT00000022425 Transcript intron_variant - - - - - - rs838712 2:234287994 C CCDS2504.1 CCDS2504.1 Transcript intron_variant - - - - - - rs838712 2:234287994 C 8527 NM_152879.2 Transcript intron_variant - - - - - - rs2063131 2:235096986 T - - - intergenic_variant - - - - - - rs4663120 2:235179644 G - - - intergenic_variant - - - - - - rs12328689 2:235263215 C - - - intergenic_variant - - - - - - rs3115357 2:235352101 A ENSESTG00000030275 ENSESTT00000076158 Transcript intron_variant - - - - - - rs3115357 2:235352101 A ENSESTG00000030383 ENSESTT00000076462 Transcript downstream_gene_variant - - - - - - DISTANCE=1133 rs1405135 2:235500840 C - - - intergenic_variant - - - - - - rs1526110 2:235594035 T - - - intergenic_variant - - - - - - rs2016911 2:235948845 C 23677 NM_014521.2 Transcript intron_variant - - - - - - rs2016911 2:235948845 C ENSESTG00000030286 ENSESTT00000076289 Transcript intron_variant - - - - - - rs2016911 2:235948845 C CCDS2513.1 CCDS2513.1 Transcript intron_variant - - - - - - rs2016911 2:235948845 C ENSESTG00000030286 ENSESTT00000076323 Transcript intron_variant - - - - - - rs4663578 2:236297503 G - - - intergenic_variant - - - - - - rs7577042 2:236348664 C - - - intergenic_variant - - - - - - rs1865945 2:236458362 G ENSESTG00000019765 ENSESTT00000049740 Transcript intron_variant - - - - - - rs1865945 2:236458362 G CCDS2514.1 CCDS2514.1 Transcript intron_variant - - - - - - rs1865945 2:236458362 G CCDS33408.1 CCDS33408.1 Transcript intron_variant - - - - - - rs1865945 2:236458362 G 116987 NM_001037131.2 Transcript intron_variant - - - - - - rs1865945 2:236458362 G ENSESTG00000019765 ENSESTT00000049732 Transcript intron_variant - - - - - - rs1865945 2:236458362 G 116987 NM_001244888.1 Transcript intron_variant - - - - - - rs1865945 2:236458362 G ENSESTG00000019765 ENSESTT00000049772 Transcript intron_variant - - - - - - rs1865945 2:236458362 G 116987 NM_014914.4 Transcript intron_variant - - - - - - rs1865945 2:236458362 G CCDS58756.1 CCDS58756.1 Transcript intron_variant - - - - - - rs6743420 2:237273331 G CCDS46549.1 CCDS46549.1 Transcript intron_variant - - - - - - rs6743420 2:237273331 G ENSESTG00000006538 ENSESTT00000016493 Transcript intron_variant - - - - - - rs6743420 2:237273331 G ENSESTG00000019916 ENSESTT00000049921 Transcript intron_variant - - - - - - rs6743420 2:237273331 G ENSESTG00000006538 ENSESTT00000016499 Transcript intron_variant - - - - - - rs6743420 2:237273331 G 79781 NM_024726.3 Transcript intron_variant - - - - - - rs6743420 2:237273331 G ENSESTG00000006538 ENSESTT00000016504 Transcript upstream_gene_variant - - - - - - DISTANCE=883 rs76336520 2:237343879 C CCDS46549.1 CCDS46549.1 Transcript intron_variant - - - - - - rs76336520 2:237343879 C ENSESTG00000006538 ENSESTT00000016493 Transcript intron_variant - - - - - - rs76336520 2:237343879 C ENSESTG00000006538 ENSESTT00000016499 Transcript intron_variant - - - - - - rs76336520 2:237343879 C 79781 NM_024726.3 Transcript intron_variant - - - - - - rs2701338 2:237912779 G - - - intergenic_variant - - - - - - rs114420547 2:239028030 G - ENSR00001553428 RegulatoryFeature regulatory_region_variant - - - - - - rs114420547 2:239028030 G ENSESTG00000016343 ENSESTT00000041013 Transcript intron_variant - - - - - - rs114420547 2:239028030 G CCDS2525.1 CCDS2525.1 Transcript intron_variant - - - - - - rs114420547 2:239028030 G ENSESTG00000016343 ENSESTT00000041005 Transcript intron_variant - - - - - - rs114420547 2:239028030 G 339768 NM_194312.2 Transcript intron_variant - - - - - - rs7578209 2:239265750 G ENSESTG00000025728 ENSESTT00000065036 Transcript intron_variant - - - - - - rs7578209 2:239265750 G CCDS46557.1 CCDS46557.1 Transcript intron_variant - - - - - - rs7578209 2:239265750 G ENSESTG00000025728 ENSESTT00000065064 Transcript intron_variant - - - - - - rs7578209 2:239265750 G 26146 NM_001139490.1 Transcript intron_variant - - - - - - rs7578209 2:239265750 G 26146 NM_015650.3 Transcript intron_variant - - - - - - rs7578209 2:239265750 G CCDS33415.1 CCDS33415.1 Transcript intron_variant - - - - - - rs7562910 2:239963743 C - - - intergenic_variant - - - - - - rs1567975 2:240261879 G 9759 NM_006037.3 Transcript intron_variant - - - - - - rs1567975 2:240261879 G CCDS2529.1 CCDS2529.1 Transcript intron_variant - - - - - - rs1567975 2:240261879 G ENSESTG00000025896 ENSESTT00000065312 Transcript intron_variant - - - - - - rs1567975 2:240261879 G ENSESTG00000025896 ENSESTT00000065334 Transcript intron_variant - - - - - - rs1567975 2:240261879 G ENSESTG00000025896 ENSESTT00000065326 Transcript intron_variant - - - - - - rs4852098 2:240531168 G - - - intergenic_variant - - - - - - rs10196018 2:240976779 G CCDS33417.1 CCDS33417.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4451 rs10196018 2:240976779 G 643905 NM_001080835.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4451 rs4854095 2:241227636 G - - - intergenic_variant - - - - - - rs4263107 2:241764685 G 547 NM_001244008.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4960 rs6745561 2:242067116 C - ENSR00000610845 RegulatoryFeature regulatory_region_variant - - - - - - rs6745561 2:242067116 C ENSESTG00000023387 ENSESTT00000059025 Transcript upstream_gene_variant - - - - - - DISTANCE=1284 rs6745561 2:242067116 C 23178 NM_015148.3 Transcript intron_variant - - - - - - rs6745561 2:242067116 C CCDS58759.1 CCDS58759.1 Transcript intron_variant - - - - - - rs6745561 2:242067116 C 23178 NM_001252124.1 Transcript intron_variant - - - - - - rs6745561 2:242067116 C 23178 NM_001252119.1 Transcript intron_variant - - - - - - rs6745561 2:242067116 C ENSESTG00000023387 ENSESTT00000059031 Transcript upstream_gene_variant - - - - - - DISTANCE=1284 rs6745561 2:242067116 C 23178 NM_001252120.1 Transcript intron_variant - - - - - - rs6745561 2:242067116 C ENSESTG00000023291 ENSESTT00000058945 Transcript intron_variant - - - - - - rs6745561 2:242067116 C CCDS58758.1 CCDS58758.1 Transcript intron_variant - - - - - - rs6745561 2:242067116 C CCDS2545.1 CCDS2545.1 Transcript intron_variant - - - - - - rs6745561 2:242067116 C 23178 NM_001252122.1 Transcript intron_variant - - - - - - rs6745561 2:242067116 C ENSESTG00000023291 ENSESTT00000058876 Transcript intron_variant - - - - - - rs1179530 2:242142737 C CCDS33423.1 CCDS33423.1 Transcript intron_variant - - - - - - rs1179530 2:242142737 C 50636 NM_001001891.3 Transcript intron_variant - - - - - - rs1179530 2:242142737 C ENSESTG00000022214 ENSESTT00000055983 Transcript downstream_gene_variant - - - - - - DISTANCE=3144 rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057934 Transcript intron_variant - - - - - - rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057666 Transcript intron_variant - - - - - - rs11891776 2:242203916 C ENSESTG00000027230 ENSESTT00000068695 Transcript downstream_gene_variant - - - - - - DISTANCE=72 rs11891776 2:242203916 C ENSESTG00000027230 ENSESTT00000068599 Transcript missense_variant 533 181 61 S/A Tct/Gct - PolyPhen=benign;SIFT=tolerated rs11891776 2:242203916 C 3069 NM_001243900.1 Transcript missense_variant 485 289 97 S/A Tct/Gct - PolyPhen=benign;SIFT=tolerated rs11891776 2:242203916 C ENSESTG00000027230 ENSESTT00000068672 Transcript downstream_gene_variant - - - - - - DISTANCE=1 rs11891776 2:242203916 C ENSESTG00000027230 ENSESTT00000068624 Transcript missense_variant 547 289 97 S/A Tct/Gct - rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057848 Transcript missense_variant 365 181 61 S/A Tct/Gct - rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057838 Transcript missense_variant 368 181 61 S/A Tct/Gct - rs11891776 2:242203916 C ENSESTG00000027230 ENSESTT00000068685 Transcript synonymous_variant 477 57 19 P ccT/ccG - rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057855 Transcript missense_variant 485 289 97 S/A Tct/Gct - rs11891776 2:242203916 C CCDS2547.1 CCDS2547.1 Transcript missense_variant 181 181 61 S/A Tct/Gct - PolyPhen=benign;SIFT=tolerated rs11891776 2:242203916 C 3069 NM_005336.4 Transcript missense_variant 414 181 61 S/A Tct/Gct - PolyPhen=benign;SIFT=tolerated rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057886 Transcript missense_variant 332 181 61 S/A Tct/Gct - rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057925 Transcript intron_variant - - - - - - rs11891776 2:242203916 C ENSESTG00000027230 ENSESTT00000068592 Transcript missense_variant 474 181 61 S/A Tct/Gct - rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057892 Transcript missense_variant 332 181 61 S/A Tct/Gct - rs11891776 2:242203916 C ENSESTG00000027230 ENSESTT00000068659 Transcript downstream_gene_variant - - - - - - DISTANCE=2326 rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057837 Transcript missense_variant 368 181 61 S/A Tct/Gct - rs11891776 2:242203916 C 3069 NM_203346.3 Transcript missense_variant 354 181 61 S/A Tct/Gct - PolyPhen=benign;SIFT=tolerated rs11891776 2:242203916 C CCDS58760.1 CCDS58760.1 Transcript missense_variant 289 289 97 S/A Tct/Gct - PolyPhen=benign;SIFT=tolerated rs11891776 2:242203916 C ENSESTG00000027230 ENSESTT00000068647 Transcript downstream_gene_variant - - - - - - DISTANCE=80 rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057638 Transcript intron_variant - - - - - - rs11891776 2:242203916 C ENSESTG00000022812 ENSESTT00000057864 Transcript missense_variant 485 289 97 S/A Tct/Gct - rs6753064 2:242893612 A ENSESTG00000026878 ENSESTT00000067741 Transcript intron_variant - - - - - - rs4973640 2:242980580 C ENSESTG00000026892 ENSESTT00000067749 Transcript intron_variant - - - - - - rs1353809 3:394348 T 10752 NM_001253388.1 Transcript intron_variant - - - - - - rs1353809 3:394348 T 10752 NM_001253387.1 Transcript intron_variant - - - - - - rs1353809 3:394348 T CCDS2556.1 CCDS2556.1 Transcript intron_variant - - - - - - rs1353809 3:394348 T ENSESTG00000007633 ENSESTT00000019252 Transcript intron_variant - - - - - - rs1353809 3:394348 T CCDS58812.1 CCDS58812.1 Transcript intron_variant - - - - - - rs1353809 3:394348 T 10752 NM_006614.3 Transcript intron_variant - - - - - - rs4684467 3:579260 A - - - intergenic_variant - - - - - - rs2729242 3:648160 A - - - intergenic_variant - - - - - - rs2731539 3:811287 A - - - intergenic_variant - - - - - - rs1403917 3:839086 C ENSESTG00000007671 ENSESTT00000019312 Transcript intron_variant - - - - - - rs4324461 3:932922 G - - - intergenic_variant - - - - - - rs4293685 3:1031452 G - - - intergenic_variant - - - - - - rs12106929 3:1217101 A CCDS2557.1 CCDS2557.1 Transcript intron_variant - - - - - - rs12106929 3:1217101 A 27255 NM_014461.2 Transcript intron_variant - - - - - - rs12106929 3:1217101 A ENSESTG00000014559 ENSESTT00000036463 Transcript intron_variant - - - - - - rs12106929 3:1217101 A ENSESTG00000014559 ENSESTT00000036451 Transcript intron_variant - - - - - - rs12106929 3:1217101 A ENSESTG00000014559 ENSESTT00000036470 Transcript intron_variant - - - - - - rs1153546 3:1506610 T - - - intergenic_variant - - - - - - rs408559 3:1663028 G ENSESTG00000014618 ENSESTT00000036568 Transcript intron_variant - - - - - - rs2678250 3:1708707 T ENSESTG00000014618 ENSESTT00000036568 Transcript intron_variant - - - - - - rs2678249 3:1708898 T ENSESTG00000014618 ENSESTT00000036568 Transcript intron_variant - - - - - - rs2731523 3:1709015 C ENSESTG00000014618 ENSESTT00000036568 Transcript intron_variant - - - - - - rs2731524 3:1709026 C ENSESTG00000014618 ENSESTT00000036568 Transcript intron_variant - - - - - - rs2731525 3:1721794 T ENSESTG00000014618 ENSESTT00000036568 Transcript intron_variant - - - - - - rs4258949 3:1801049 A - - - intergenic_variant - - - - - - rs9809072 3:1826650 G - - - intergenic_variant - - - - - - rs1906634 3:1940775 T - - - intergenic_variant - - - - - - rs1488748 3:2010713 T ENSESTG00000015812 ENSESTT00000039621 Transcript intron_variant - - - - - - rs2729302 3:2024146 A ENSESTG00000015812 ENSESTT00000039621 Transcript intron_variant - - - - - - rs2729022 3:2083775 T - - - intergenic_variant - - - - - - rs4684329 3:2113743 G - - - intergenic_variant - - - - - - rs2728525 3:2212634 G 152330 NM_175607.2 Transcript intron_variant - - - - - - rs13070038 3:2423539 A 152330 NM_001206955.1 Transcript intron_variant - - - - - - rs13070038 3:2423539 A 152330 NM_175607.2 Transcript intron_variant - - - - - - rs9819029 3:2423635 A 152330 NM_001206955.1 Transcript intron_variant - - - - - - rs9819029 3:2423635 A 152330 NM_175607.2 Transcript intron_variant - - - - - - rs1502590 3:2449167 A 152330 NM_001206955.1 Transcript intron_variant - - - - - - rs1502590 3:2449167 A 152330 NM_175607.2 Transcript intron_variant - - - - - - rs57536535 3:2586911 T ENSESTG00000015745 ENSESTT00000039430 Transcript intron_variant - - - - - - rs57536535 3:2586911 T 152330 NM_001206955.1 Transcript intron_variant - - - - - - rs57536535 3:2586911 T ENSESTG00000015745 ENSESTT00000039416 Transcript intron_variant - - - - - - rs57536535 3:2586911 T 152330 NM_175607.2 Transcript intron_variant - - - - - - rs57536535 3:2586911 T ENSESTG00000015745 ENSESTT00000039422 Transcript intron_variant - - - - - - rs6799601 3:2589628 T ENSESTG00000015745 ENSESTT00000039430 Transcript intron_variant - - - - - - rs6799601 3:2589628 T 152330 NM_001206955.1 Transcript intron_variant - - - - - - rs6799601 3:2589628 T ENSESTG00000015745 ENSESTT00000039416 Transcript intron_variant - - - - - - rs6799601 3:2589628 T 152330 NM_175607.2 Transcript intron_variant - - - - - - rs6799601 3:2589628 T ENSESTG00000015745 ENSESTT00000039422 Transcript intron_variant - - - - - - rs2046036 3:2630262 G ENSESTG00000015745 ENSESTT00000039430 Transcript intron_variant - - - - - - rs2046036 3:2630262 G 152330 NM_001206955.1 Transcript intron_variant - - - - - - rs2046036 3:2630262 G ENSESTG00000015745 ENSESTT00000039416 Transcript intron_variant - - - - - - rs2046036 3:2630262 G 152330 NM_175607.2 Transcript intron_variant - - - - - - rs2046036 3:2630262 G CCDS43041.1 CCDS43041.1 Transcript intron_variant - - - - - - rs2046036 3:2630262 G ENSESTG00000015745 ENSESTT00000039422 Transcript intron_variant - - - - - - rs9848877 3:2793590 T 152330 NM_001206955.1 Transcript intron_variant - - - - - - rs9848877 3:2793590 T 152330 NM_175607.2 Transcript intron_variant - - - - - - rs9848877 3:2793590 T CCDS43041.1 CCDS43041.1 Transcript intron_variant - - - - - - rs9848877 3:2793590 T ENSESTG00000015745 ENSESTT00000039462 Transcript intron_variant - - - - - - rs340818 3:3028805 G 152330 NM_001206955.1 Transcript intron_variant - - - - - - rs340818 3:3028805 G 152330 NM_175607.2 Transcript intron_variant - - - - - - rs340818 3:3028805 G 152330 NM_175613.2 Transcript intron_variant - - - - - - rs340818 3:3028805 G CCDS2558.1 CCDS2558.1 Transcript intron_variant - - - - - - rs340818 3:3028805 G ENSESTG00000005888 ENSESTT00000014948 Transcript upstream_gene_variant - - - - - - DISTANCE=1255 rs340818 3:3028805 G ENSESTG00000015745 ENSESTT00000039462 Transcript intron_variant - - - - - - rs340818 3:3028805 G CCDS43041.1 CCDS43041.1 Transcript intron_variant - - - - - - rs340818 3:3028805 G 152330 NM_001206956.1 Transcript intron_variant - - - - - - rs340818 3:3028805 G ENSESTG00000015745 ENSESTT00000039481 Transcript intron_variant - - - - - - rs163555 3:3048336 T 152330 NM_001206955.1 Transcript intron_variant - - - - - - rs163555 3:3048336 T 152330 NM_175607.2 Transcript intron_variant - - - - - - rs163555 3:3048336 T 152330 NM_175613.2 Transcript intron_variant - - - - - - rs163555 3:3048336 T CCDS2558.1 CCDS2558.1 Transcript intron_variant - - - - - - rs163555 3:3048336 T ENSESTG00000005888 ENSESTT00000014948 Transcript intron_variant - - - - - - rs163555 3:3048336 T ENSESTG00000015745 ENSESTT00000039462 Transcript intron_variant - - - - - - rs163555 3:3048336 T CCDS43041.1 CCDS43041.1 Transcript intron_variant - - - - - - rs163555 3:3048336 T 152330 NM_001206956.1 Transcript intron_variant - - - - - - rs334755 3:3185063 G ENSESTG00000005916 ENSESTT00000015011 Transcript downstream_gene_variant - - - - - - DISTANCE=2658 rs334755 3:3185063 G ENSESTG00000005916 ENSESTT00000015010 Transcript intron_variant - - - - - - rs334755 3:3185063 G CCDS2561.2 CCDS2561.2 Transcript intron_variant - - - - - - rs334755 3:3185063 G 51095 NM_182916.2 Transcript intron_variant - - - - - - rs1672764 3:3203419 A ENSESTG00000005948 ENSESTT00000015110 Transcript intron_variant - - - - - - rs1672764 3:3203419 A 51185 NM_016302.3 Transcript intron_variant - - - - - - rs1672764 3:3203419 A CCDS54547.1 CCDS54547.1 Transcript intron_variant - - - - - - rs1672764 3:3203419 A 51185 NM_001173482.1 Transcript intron_variant - - - - - - rs1672764 3:3203419 A CCDS2562.1 CCDS2562.1 Transcript intron_variant - - - - - - rs1672764 3:3203419 A ENSESTG00000005948 ENSESTT00000015104 Transcript intron_variant - - - - - - rs967964 3:3236698 G - - - intergenic_variant - - - - - - rs1995195 3:3363134 A - - - intergenic_variant - - - - - - rs1995197 3:3367276 G - - - intergenic_variant - - - - - - rs9842034 3:3390632 T - - - intergenic_variant - - - - - - rs1921018 3:3656906 G - - - intergenic_variant - - - - - - rs4309713 3:3695526 G - - - intergenic_variant - - - - - - rs4333072 3:3696585 T - - - intergenic_variant - - - - - - rs4478068 3:3701836 G - - - intergenic_variant - - - - - - rs7631653 3:3703510 G - - - intergenic_variant - - - - - - rs769811 3:3717754 T - - - intergenic_variant - - - - - - rs711573 3:3721772 A - - - intergenic_variant - - - - - - rs2584061 3:3736890 G - - - intergenic_variant - - - - - - rs2629287 3:3760254 C - - - intergenic_variant - - - - - - rs2584056 3:3760305 T - - - intergenic_variant - - - - - - rs698199 3:3785196 A - - - intergenic_variant - - - - - - rs2600147 3:4180728 A - - - intergenic_variant - - - - - - rs2600146 3:4180769 A - - - intergenic_variant - - - - - - rs2600145 3:4182665 T - - - intergenic_variant - - - - - - rs1586266 3:4249585 T - - - intergenic_variant - - - - - - rs2582340 3:4443475 T 285362 NM_001164675.1 Transcript intron_variant - - - - - - rs2582340 3:4443475 T ENSESTG00000031799 ENSESTT00000080262 Transcript intron_variant - - - - - - rs2582340 3:4443475 T CCDS54549.1 CCDS54549.1 Transcript intron_variant - - - - - - rs2582340 3:4443475 T ENSESTG00000031799 ENSESTT00000080354 Transcript intron_variant - - - - - - rs2582340 3:4443475 T ENSESTG00000031799 ENSESTT00000080331 Transcript intron_variant - - - - - - rs2582340 3:4443475 T CCDS54548.1 CCDS54548.1 Transcript intron_variant - - - - - - rs2582340 3:4443475 T 285362 NM_001164674.1 Transcript intron_variant - - - - - - rs2582340 3:4443475 T ENSESTG00000031799 ENSESTT00000080325 Transcript intron_variant - - - - - - rs2582340 3:4443475 T 285362 NM_182760.3 Transcript intron_variant - - - - - - rs2582340 3:4443475 T CCDS2564.1 CCDS2564.1 Transcript intron_variant - - - - - - rs2819576 3:4478069 A 285362 NM_001164675.1 Transcript intron_variant - - - - - - rs2819576 3:4478069 A ENSESTG00000031799 ENSESTT00000080262 Transcript intron_variant - - - - - - rs2819576 3:4478069 A CCDS54549.1 CCDS54549.1 Transcript intron_variant - - - - - - rs2819576 3:4478069 A ENSESTG00000031799 ENSESTT00000080354 Transcript intron_variant - - - - - - rs2819576 3:4478069 A ENSESTG00000031799 ENSESTT00000080331 Transcript intron_variant - - - - - - rs2819576 3:4478069 A ENSESTG00000031799 ENSESTT00000080340 Transcript intron_variant - - - - - - rs2819576 3:4478069 A CCDS54548.1 CCDS54548.1 Transcript intron_variant - - - - - - rs2819576 3:4478069 A 285362 NM_001164674.1 Transcript intron_variant - - - - - - rs2819576 3:4478069 A ENSESTG00000031799 ENSESTT00000080325 Transcript intron_variant - - - - - - rs2819576 3:4478069 A CCDS2564.1 CCDS2564.1 Transcript intron_variant - - - - - - rs2819576 3:4478069 A 285362 NM_182760.3 Transcript intron_variant - - - - - - rs2819575 3:4480541 T 285362 NM_001164675.1 Transcript intron_variant - - - - - - rs2819575 3:4480541 T ENSESTG00000031799 ENSESTT00000080262 Transcript intron_variant - - - - - - rs2819575 3:4480541 T CCDS54549.1 CCDS54549.1 Transcript intron_variant - - - - - - rs2819575 3:4480541 T ENSESTG00000031799 ENSESTT00000080354 Transcript intron_variant - - - - - - rs2819575 3:4480541 T ENSESTG00000031799 ENSESTT00000080331 Transcript intron_variant - - - - - - rs2819575 3:4480541 T ENSESTG00000031799 ENSESTT00000080340 Transcript intron_variant - - - - - - rs2819575 3:4480541 T CCDS54548.1 CCDS54548.1 Transcript intron_variant - - - - - - rs2819575 3:4480541 T 285362 NM_001164674.1 Transcript intron_variant - - - - - - rs2819575 3:4480541 T ENSESTG00000031799 ENSESTT00000080325 Transcript intron_variant - - - - - - rs2819575 3:4480541 T CCDS2564.1 CCDS2564.1 Transcript intron_variant - - - - - - rs2819575 3:4480541 T 285362 NM_182760.3 Transcript intron_variant - - - - - - rs304059 3:4573672 A - ENSR00001356274 RegulatoryFeature regulatory_region_variant - - - - - - rs304059 3:4573672 A 3708 NM_001168272.1 Transcript intron_variant - - - - - - rs304059 3:4573672 A CCDS46740.2 CCDS46740.2 Transcript intron_variant - - - - - - rs304059 3:4573672 A ENSESTG00000031550 ENSESTT00000079568 Transcript intron_variant - - - - - - rs304059 3:4573672 A CCDS54550.1 CCDS54550.1 Transcript intron_variant - - - - - - rs304059 3:4573672 A 3708 NM_002222.5 Transcript intron_variant - - - - - - rs304059 3:4573672 A 3708 NM_001099952.2 Transcript intron_variant - - - - - - rs304059 3:4573672 A CCDS54551.1 CCDS54551.1 Transcript intron_variant - - - - - - rs2470502 3:4654136 A 3708 NM_001168272.1 Transcript intron_variant - - - - - - rs2470502 3:4654136 A CCDS46740.2 CCDS46740.2 Transcript intron_variant - - - - - - rs2470502 3:4654136 A ENSESTG00000031550 ENSESTT00000079568 Transcript intron_variant - - - - - - rs2470502 3:4654136 A CCDS54550.1 CCDS54550.1 Transcript intron_variant - - - - - - rs2470502 3:4654136 A 3708 NM_002222.5 Transcript intron_variant - - - - - - rs2470502 3:4654136 A 3708 NM_001099952.2 Transcript intron_variant - - - - - - rs2470502 3:4654136 A CCDS54551.1 CCDS54551.1 Transcript intron_variant - - - - - - rs4685787 3:4685357 A 3708 NM_001168272.1 Transcript intron_variant - - - - - - rs4685787 3:4685357 A CCDS54550.1 CCDS54550.1 Transcript intron_variant - - - - - - rs4685787 3:4685357 A ENSESTG00000031561 ENSESTT00000079593 Transcript intron_variant - - - - - - rs4685787 3:4685357 A ENSESTG00000031561 ENSESTT00000079597 Transcript upstream_gene_variant - - - - - - DISTANCE=474 rs4685787 3:4685357 A 3708 NM_001099952.2 Transcript intron_variant - - - - - - rs4685787 3:4685357 A CCDS46740.2 CCDS46740.2 Transcript intron_variant - - - - - - rs4685787 3:4685357 A 3708 NM_002222.5 Transcript intron_variant - - - - - - rs4685787 3:4685357 A CCDS54551.1 CCDS54551.1 Transcript intron_variant - - - - - - rs4685794 3:4700787 A 3708 NM_001168272.1 Transcript intron_variant - - - - - - rs4685794 3:4700787 A CCDS46740.2 CCDS46740.2 Transcript intron_variant - - - - - - rs4685794 3:4700787 A CCDS54550.1 CCDS54550.1 Transcript intron_variant - - - - - - rs4685794 3:4700787 A ENSESTG00000031561 ENSESTT00000079593 Transcript downstream_gene_variant - - - - - - DISTANCE=956 rs4685794 3:4700787 A 3708 NM_002222.5 Transcript intron_variant - - - - - - rs4685794 3:4700787 A 3708 NM_001099952.2 Transcript intron_variant - - - - - - rs4685794 3:4700787 A CCDS54551.1 CCDS54551.1 Transcript intron_variant - - - - - - rs6798315 3:4749661 A 3708 NM_001168272.1 Transcript intron_variant - - - - - - rs6798315 3:4749661 A CCDS46740.2 CCDS46740.2 Transcript intron_variant - - - - - - rs6798315 3:4749661 A CCDS54550.1 CCDS54550.1 Transcript intron_variant - - - - - - rs6798315 3:4749661 A ENSESTG00000031618 ENSESTT00000080042 Transcript intron_variant - - - - - - rs6798315 3:4749661 A 3708 NM_002222.5 Transcript intron_variant - - - - - - rs6798315 3:4749661 A 3708 NM_001099952.2 Transcript intron_variant - - - - - - rs6798315 3:4749661 A CCDS54551.1 CCDS54551.1 Transcript intron_variant - - - - - - rs6798320 3:4749674 A 3708 NM_001168272.1 Transcript intron_variant - - - - - - rs6798320 3:4749674 A CCDS46740.2 CCDS46740.2 Transcript intron_variant - - - - - - rs6798320 3:4749674 A CCDS54550.1 CCDS54550.1 Transcript intron_variant - - - - - - rs6798320 3:4749674 A ENSESTG00000031618 ENSESTT00000080042 Transcript intron_variant - - - - - - rs6798320 3:4749674 A 3708 NM_002222.5 Transcript intron_variant - - - - - - rs6798320 3:4749674 A 3708 NM_001099952.2 Transcript intron_variant - - - - - - rs6798320 3:4749674 A CCDS54551.1 CCDS54551.1 Transcript intron_variant - - - - - - rs13080185 3:4771489 A 3708 NM_001168272.1 Transcript intron_variant - - - - - - rs13080185 3:4771489 A CCDS54550.1 CCDS54550.1 Transcript intron_variant - - - - - - rs13080185 3:4771489 A ENSESTG00000031618 ENSESTT00000080042 Transcript intron_variant - - - - - - rs13080185 3:4771489 A 3708 NM_001099952.2 Transcript intron_variant - - - - - - rs13080185 3:4771489 A CCDS46740.2 CCDS46740.2 Transcript intron_variant - - - - - - rs13080185 3:4771489 A 3708 NM_002222.5 Transcript intron_variant - - - - - - rs13080185 3:4771489 A ENSESTG00000031618 ENSESTT00000080052 Transcript intron_variant - - - - - - rs13080185 3:4771489 A CCDS54551.1 CCDS54551.1 Transcript intron_variant - - - - - - rs1145126 3:4821999 T 3708 NM_001168272.1 Transcript intron_variant - - - - - - rs1145126 3:4821999 T CCDS54550.1 CCDS54550.1 Transcript intron_variant - - - - - - rs1145126 3:4821999 T ENSESTG00000031618 ENSESTT00000080042 Transcript intron_variant - - - - - - rs1145126 3:4821999 T 3708 NM_001099952.2 Transcript intron_variant - - - - - - rs1145126 3:4821999 T CCDS46740.2 CCDS46740.2 Transcript intron_variant - - - - - - rs1145126 3:4821999 T 3708 NM_002222.5 Transcript intron_variant - - - - - - rs1145126 3:4821999 T ENSESTG00000031618 ENSESTT00000080062 Transcript intron_variant - - - - - - rs1145126 3:4821999 T CCDS54551.1 CCDS54551.1 Transcript intron_variant - - - - - - rs9878097 3:4924631 C ENSESTG00000031784 ENSESTT00000080209 Transcript intron_variant - - - - - - rs2470560 3:5075903 G - - - intergenic_variant - - - - - - rs4234567 3:5445452 A - - - intergenic_variant - - - - - - rs4423751 3:5473411 C - - - intergenic_variant - - - - - - rs4685946 3:5600990 G - - - intergenic_variant - - - - - - rs925858 3:6007751 C - - - intergenic_variant - - - - - - rs6443015 3:6070957 T - - - intergenic_variant - - - - - - rs6443020 3:6115184 T - - - intergenic_variant - - - - - - rs1245374 3:6193447 T - - - intergenic_variant - - - - - - rs1245373 3:6200095 C - - - intergenic_variant - - - - - - rs286584 3:6219312 A - - - intergenic_variant - - - - - - rs2575002 3:6252640 C - - - intergenic_variant - - - - - - rs788181 3:6306740 T - - - intergenic_variant - - - - - - rs1695304 3:6322979 A - - - intergenic_variant - - - - - - rs1656567 3:6322983 A - - - intergenic_variant - - - - - - rs712747 3:6323021 A - - - intergenic_variant - - - - - - rs149516 3:6519202 C - - - intergenic_variant - - - - - - rs345201 3:6803342 T ENSESTG00000018392 ENSESTT00000046312 Transcript intron_variant - - - - - - rs345201 3:6803342 T ENSESTG00000018392 ENSESTT00000046337 Transcript intron_variant - - - - - - rs345201 3:6803342 T ENSESTG00000018392 ENSESTT00000046328 Transcript intron_variant - - - - - - rs345201 3:6803342 T ENSESTG00000018392 ENSESTT00000046354 Transcript intron_variant - - - - - - rs345201 3:6803342 T ENSESTG00000018392 ENSESTT00000046298 Transcript intron_variant - - - - - - rs711632 3:6982700 A 2917 NM_000844.3 Transcript intron_variant - - - - - - rs711632 3:6982700 A 2917 NM_181874.2 Transcript intron_variant - - - - - - rs711632 3:6982700 A CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs711632 3:6982700 A ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs168119 3:6994924 T 2917 NM_000844.3 Transcript intron_variant - - - - - - rs168119 3:6994924 T 2917 NM_181874.2 Transcript intron_variant - - - - - - rs168119 3:6994924 T CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs168119 3:6994924 T ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs11131062 3:7140716 C 2917 NM_000844.3 Transcript intron_variant - - - - - - rs11131062 3:7140716 C 2917 NM_181874.2 Transcript intron_variant - - - - - - rs11131062 3:7140716 C CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs11131062 3:7140716 C ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs63214062 3:7179622 A 2917 NM_000844.3 Transcript intron_variant - - - - - - rs63214062 3:7179622 A 2917 NM_181874.2 Transcript intron_variant - - - - - - rs63214062 3:7179622 A CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs63214062 3:7179622 A ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs2648635 3:7219128 T 2917 NM_000844.3 Transcript intron_variant - - - - - - rs2648635 3:7219128 T 2917 NM_181874.2 Transcript intron_variant - - - - - - rs2648635 3:7219128 T CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs2648635 3:7219128 T ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs1396412 3:7239241 A 2917 NM_000844.3 Transcript intron_variant - - - - - - rs1396412 3:7239241 A 2917 NM_181874.2 Transcript intron_variant - - - - - - rs1396412 3:7239241 A CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs1396412 3:7239241 A ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs9809921 3:7302332 A 2917 NM_000844.3 Transcript intron_variant - - - - - - rs9809921 3:7302332 A 2917 NM_181874.2 Transcript intron_variant - - - - - - rs9809921 3:7302332 A CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs9809921 3:7302332 A ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs4470504 3:7302823 G 2917 NM_000844.3 Transcript intron_variant - - - - - - rs4470504 3:7302823 G 2917 NM_181874.2 Transcript intron_variant - - - - - - rs4470504 3:7302823 G CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs4470504 3:7302823 G ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs4479583 3:7305033 G 2917 NM_000844.3 Transcript intron_variant - - - - - - rs4479583 3:7305033 G 2917 NM_181874.2 Transcript intron_variant - - - - - - rs4479583 3:7305033 G CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs4479583 3:7305033 G ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs4399874 3:7305635 G 2917 NM_000844.3 Transcript intron_variant - - - - - - rs4399874 3:7305635 G 2917 NM_181874.2 Transcript intron_variant - - - - - - rs4399874 3:7305635 G CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs4399874 3:7305635 G ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs9821672 3:7402670 C ENSESTG00000015202 ENSESTT00000038058 Transcript intron_variant - - - - - - rs9821672 3:7402670 C 2917 NM_000844.3 Transcript intron_variant - - - - - - rs9821672 3:7402670 C 2917 NM_181874.2 Transcript intron_variant - - - - - - rs9821672 3:7402670 C CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs9821672 3:7402670 C ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs9311989 3:7407012 T ENSESTG00000015202 ENSESTT00000038058 Transcript intron_variant - - - - - - rs9311989 3:7407012 T 2917 NM_000844.3 Transcript intron_variant - - - - - - rs9311989 3:7407012 T 2917 NM_181874.2 Transcript intron_variant - - - - - - rs9311989 3:7407012 T CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs9311989 3:7407012 T ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs8180002 3:7420351 A ENSESTG00000015202 ENSESTT00000038058 Transcript intron_variant - - - - - - rs8180002 3:7420351 A 2917 NM_000844.3 Transcript intron_variant - - - - - - rs8180002 3:7420351 A 2917 NM_181874.2 Transcript intron_variant - - - - - - rs8180002 3:7420351 A CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs8180002 3:7420351 A ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs1272450 3:7434543 T ENSESTG00000015202 ENSESTT00000038058 Transcript intron_variant - - - - - - rs1272450 3:7434543 T 2917 NM_000844.3 Transcript intron_variant - - - - - - rs1272450 3:7434543 T 2917 NM_181874.2 Transcript intron_variant - - - - - - rs1272450 3:7434543 T CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs1272450 3:7434543 T ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs2648647 3:7436373 C ENSESTG00000015202 ENSESTT00000038058 Transcript intron_variant - - - - - - rs2648647 3:7436373 C 2917 NM_000844.3 Transcript intron_variant - - - - - - rs2648647 3:7436373 C 2917 NM_181874.2 Transcript intron_variant - - - - - - rs2648647 3:7436373 C CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs2648647 3:7436373 C ENSESTG00000018367 ENSESTT00000046223 Transcript intron_variant - - - - - - rs6443122 3:7710311 A ENSESTG00000015228 ENSESTT00000038122 Transcript intron_variant - - - - - - rs6443122 3:7710311 A 2917 NM_000844.3 Transcript intron_variant - - - - - - rs6443122 3:7710311 A 2917 NM_181874.2 Transcript intron_variant - - - - - - rs6443122 3:7710311 A CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs2031057 3:7710712 G ENSESTG00000015228 ENSESTT00000038122 Transcript intron_variant - - - - - - rs2031057 3:7710712 G 2917 NM_000844.3 Transcript intron_variant - - - - - - rs2031057 3:7710712 G 2917 NM_181874.2 Transcript intron_variant - - - - - - rs2031057 3:7710712 G CCDS43042.1 CCDS43042.1 Transcript intron_variant - - - - - - rs9845398 3:7962952 T - - - intergenic_variant - - - - - - rs4686195 3:7968719 T - - - intergenic_variant - - - - - - rs4305414 3:8114463 C - - - intergenic_variant - - - - - - rs2633810 3:8292719 C 100288428 NR_033378.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4686254 3:8381100 T 100288428 NR_033378.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4686255 3:8381194 T 100288428 NR_033378.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2629224 3:8423619 T 100288428 NR_033378.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2629210 3:8454732 C 100288428 NR_033378.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2629211 3:8455374 T 100288428 NR_033378.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2662097 3:8642114 G - - - intergenic_variant - - - - - - rs2737181 3:8690869 A 51066 NM_001256748.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4385 rs2737181 3:8690869 A CCDS58815.1 CCDS58815.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4425 rs2737181 3:8690869 A 51066 NM_001256749.1 Transcript intron_variant - - - - - - rs2737181 3:8690869 A 51066 NM_015931.2 Transcript intron_variant - - - - - - rs2737181 3:8690869 A ENSESTG00000026513 ENSESTT00000066782 Transcript intron_variant - - - - - - rs2737181 3:8690869 A ENSESTG00000026513 ENSESTT00000066836 Transcript upstream_gene_variant - - - - - - DISTANCE=4389 rs2737181 3:8690869 A ENSESTG00000026513 ENSESTT00000066803 Transcript upstream_gene_variant - - - - - - DISTANCE=4385 rs2737181 3:8690869 A ENSESTG00000026513 ENSESTT00000066759 Transcript intron_variant - - - - - - rs2737181 3:8690869 A ENSESTG00000026513 ENSESTT00000066819 Transcript upstream_gene_variant - - - - - - DISTANCE=4385 rs2737181 3:8690869 A 51066 NR_046358.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4385 rs237863 3:8773525 G 859 NM_001234.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1961 rs237863 3:8773525 G ENSESTG00000026409 ENSESTT00000066528 Transcript upstream_gene_variant - - - - - - DISTANCE=1961 rs237863 3:8773525 G 859 NM_033337.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1961 rs237863 3:8773525 G CCDS2569.1 CCDS2569.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2038 rs237863 3:8773525 G ENSESTG00000026495 ENSESTT00000066737 Transcript intron_variant - - - - - - rs2662095 3:9043631 A 9901 NM_001033117.2 Transcript intron_variant - - - - - - rs2662095 3:9043631 A ENSESTG00000011012 ENSESTT00000027636 Transcript intron_variant - - - - - - rs2662095 3:9043631 A ENSESTG00000011012 ENSESTT00000027642 Transcript intron_variant - - - - - - rs2662095 3:9043631 A CCDS33689.1 CCDS33689.1 Transcript intron_variant - - - - - - rs2662095 3:9043631 A CCDS2572.1 CCDS2572.1 Transcript intron_variant - - - - - - rs2662095 3:9043631 A 9901 NM_014850.3 Transcript intron_variant - - - - - - rs2662093 3:9045548 C 9901 NM_001033117.2 Transcript intron_variant - - - - - - rs2662093 3:9045548 C ENSESTG00000011012 ENSESTT00000027636 Transcript intron_variant - - - - - - rs2662093 3:9045548 C ENSESTG00000011012 ENSESTT00000027642 Transcript intron_variant - - - - - - rs2662093 3:9045548 C CCDS33689.1 CCDS33689.1 Transcript intron_variant - - - - - - rs2662093 3:9045548 C CCDS2572.1 CCDS2572.1 Transcript intron_variant - - - - - - rs2662093 3:9045548 C 9901 NM_014850.3 Transcript intron_variant - - - - - - rs2662092 3:9045566 G 9901 NM_001033117.2 Transcript intron_variant - - - - - - rs2662092 3:9045566 G ENSESTG00000011012 ENSESTT00000027636 Transcript intron_variant - - - - - - rs2662092 3:9045566 G ENSESTG00000011012 ENSESTT00000027642 Transcript intron_variant - - - - - - rs2662092 3:9045566 G CCDS33689.1 CCDS33689.1 Transcript intron_variant - - - - - - rs2662092 3:9045566 G CCDS2572.1 CCDS2572.1 Transcript intron_variant - - - - - - rs2662092 3:9045566 G 9901 NM_014850.3 Transcript intron_variant - - - - - - rs2617113 3:9045576 C 9901 NM_001033117.2 Transcript intron_variant - - - - - - rs2617113 3:9045576 C ENSESTG00000011012 ENSESTT00000027636 Transcript intron_variant - - - - - - rs2617113 3:9045576 C ENSESTG00000011012 ENSESTT00000027642 Transcript intron_variant - - - - - - rs2617113 3:9045576 C CCDS33689.1 CCDS33689.1 Transcript intron_variant - - - - - - rs2617113 3:9045576 C CCDS2572.1 CCDS2572.1 Transcript intron_variant - - - - - - rs2617113 3:9045576 C 9901 NM_014850.3 Transcript intron_variant - - - - - - rs374210 3:9077586 T 9901 NM_001033117.2 Transcript intron_variant - - - - - - rs374210 3:9077586 T ENSESTG00000011012 ENSESTT00000027636 Transcript intron_variant - - - - - - rs374210 3:9077586 T CCDS33689.1 CCDS33689.1 Transcript intron_variant - - - - - - rs374210 3:9077586 T CCDS2572.1 CCDS2572.1 Transcript intron_variant - - - - - - rs374210 3:9077586 T 9901 NM_014850.3 Transcript intron_variant - - - - - - rs2648525 3:9279214 T 9901 NM_001033117.2 Transcript intron_variant - - - - - - rs2648525 3:9279214 T ENSESTG00000011001 ENSESTT00000027585 Transcript intron_variant - - - - - - rs2648525 3:9279214 T CCDS33689.1 CCDS33689.1 Transcript intron_variant - - - - - - rs2648525 3:9279214 T CCDS2572.1 CCDS2572.1 Transcript intron_variant - - - - - - rs2648525 3:9279214 T 9901 NM_014850.3 Transcript intron_variant - - - - - - rs2648392 3:9593384 C 375323 NM_198560.2 Transcript intron_variant - - - - - - rs2648392 3:9593384 C CCDS33691.1 CCDS33691.1 Transcript intron_variant - - - - - - rs6783252 3:9966595 C ENSESTG00000014223 ENSESTT00000035688 Transcript upstream_gene_variant - - - - - - DISTANCE=4837 rs6783252 3:9966595 C ENSESTG00000014223 ENSESTT00000035653 Transcript downstream_gene_variant - - - - - - DISTANCE=780 rs6783252 3:9966595 C ENSESTG00000010891 ENSESTT00000027285 Transcript intron_variant - - - - - - rs6783252 3:9966595 C CCDS46746.1 CCDS46746.1 Transcript intron_variant - - - - - - rs6783252 3:9966595 C 84818 NM_001203265.1 Transcript intron_variant - - - - - - rs6783252 3:9966595 C CCDS2590.1 CCDS2590.1 Transcript intron_variant - - - - - - rs6783252 3:9966595 C 84818 NM_001203264.1 Transcript intron_variant - - - - - - rs6783252 3:9966595 C 84818 NM_001203263.1 Transcript intron_variant - - - - - - rs6783252 3:9966595 C 84818 NM_153461.3 Transcript intron_variant - - - - - - rs6783252 3:9966595 C CCDS2591.2 CCDS2591.2 Transcript intron_variant - - - - - - rs6783252 3:9966595 C ENSESTG00000014223 ENSESTT00000035681 Transcript upstream_gene_variant - - - - - - DISTANCE=3514 rs6783252 3:9966595 C 84818 NM_032732.5 Transcript intron_variant - - - - - - rs6783252 3:9966595 C 84818 NM_153460.3 Transcript intron_variant - - - - - - rs6783252 3:9966595 C CCDS56240.1 CCDS56240.1 Transcript intron_variant - - - - - - rs6783252 3:9966595 C CCDS56241.1 CCDS56241.1 Transcript intron_variant - - - - - - rs6783252 3:9966595 C ENSESTG00000014223 ENSESTT00000035648 Transcript intron_variant - - - - - - rs6783252 3:9966595 C 84818 NR_037807.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs401900 3:10117832 G ENSESTG00000014350 ENSESTT00000036094 Transcript intron_variant - - - - - - rs401900 3:10117832 G ENSESTG00000014350 ENSESTT00000036088 Transcript intron_variant - - - - - - rs401900 3:10117832 G ENSESTG00000014350 ENSESTT00000036058 Transcript intron_variant - - - - - - rs401900 3:10117832 G ENSESTG00000014350 ENSESTT00000035979 Transcript intron_variant - - - - - - rs401900 3:10117832 G CCDS2595.1 CCDS2595.1 Transcript intron_variant - - - - - - rs401900 3:10117832 G ENSESTG00000014350 ENSESTT00000036097 Transcript intron_variant - - - - - - rs401900 3:10117832 G CCDS33696.1 CCDS33696.1 Transcript intron_variant - - - - - - rs401900 3:10117832 G 2177 NM_033084.3 Transcript intron_variant - - - - - - rs401900 3:10117832 G ENSESTG00000014350 ENSESTT00000035964 Transcript intron_variant - - - - - - rs401900 3:10117832 G 2177 NM_001018115.1 Transcript intron_variant - - - - - - rs2544007 3:10324750 T CCDS46750.1 CCDS46750.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2809 rs2544007 3:10324750 T CCDS46748.1 CCDS46748.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2809 rs2544007 3:10324750 T 100126793 NR_024144.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2688 rs2544007 3:10324750 T 51738 NR_024136.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T 100126793 NR_024146.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2688 rs2544007 3:10324750 T 51738 NM_001134945.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T 51738 NM_016362.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T 51738 NM_001134944.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T ENSESTG00000014648 ENSESTT00000036659 Transcript upstream_gene_variant - - - - - - DISTANCE=1848 rs2544007 3:10324750 T 51738 NR_024135.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T CCDS46747.1 CCDS46747.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2809 rs2544007 3:10324750 T 51738 NM_001134941.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T CCDS46749.1 CCDS46749.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2809 rs2544007 3:10324750 T 100126793 NR_024145.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2688 rs2544007 3:10324750 T 51738 NR_024137.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T CCDS33698.1 CCDS33698.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4041 rs2544007 3:10324750 T 100126793 NR_004431.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2688 rs2544007 3:10324750 T 51738 NR_024134.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T 84657 NR_026829.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1353 rs2544007 3:10324750 T 51738 NM_001134946.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T ENSESTG00000014488 ENSESTT00000036304 Transcript downstream_gene_variant - - - - - - DISTANCE=3902 rs2544007 3:10324750 T 51738 NR_024133.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T 51738 NR_024132.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T CCDS33700.1 CCDS33700.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2809 rs2544007 3:10324750 T ENSESTG00000014503 ENSESTT00000036312 Transcript upstream_gene_variant - - - - - - DISTANCE=2722 rs2544007 3:10324750 T 51738 NR_024138.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2684 rs2544007 3:10324750 T 9797 NM_014760.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1844 rs2577800 3:10372429 C 100422933 NR_036084.1 Transcript downstream_gene_variant - - - - - - DISTANCE=460 rs2577800 3:10372429 C CCDS33701.1 CCDS33701.1 Transcript intron_variant - - - - - - rs2577800 3:10372429 C CCDS2601.1 CCDS2601.1 Transcript intron_variant - - - - - - rs2577800 3:10372429 C 491 NM_001683.3 Transcript intron_variant - - - - - - rs2577800 3:10372429 C ENSESTG00000014580 ENSESTT00000036497 Transcript intron_variant - - - - - - rs2577800 3:10372429 C 491 NM_001001331.2 Transcript intron_variant - - - - - - rs2577800 3:10372429 C ENSESTG00000014580 ENSESTT00000036517 Transcript intron_variant - - - - - - rs2470452 3:10385345 T ENSESTG00000014557 ENSESTT00000036460 Transcript downstream_gene_variant - - - - - - DISTANCE=2449 rs2470452 3:10385345 T CCDS33701.1 CCDS33701.1 Transcript intron_variant - - - - - - rs2470452 3:10385345 T CCDS2601.1 CCDS2601.1 Transcript intron_variant - - - - - - rs2470452 3:10385345 T 491 NM_001683.3 Transcript intron_variant - - - - - - rs2470452 3:10385345 T ENSESTG00000014580 ENSESTT00000036497 Transcript upstream_gene_variant - - - - - - DISTANCE=890 rs2470452 3:10385345 T 491 NM_001001331.2 Transcript intron_variant - - - - - - rs2470452 3:10385345 T ENSESTG00000014580 ENSESTT00000036517 Transcript upstream_gene_variant - - - - - - DISTANCE=3002 rs12494619 3:10530336 C ENSESTG00000014542 ENSESTT00000036401 Transcript intron_variant - - - - - - rs12494619 3:10530336 C 491 NM_001683.3 Transcript intron_variant - - - - - - rs12494619 3:10530336 C 491 NM_001001331.2 Transcript intron_variant - - - - - - rs7614761 3:10543438 C ENSESTG00000014542 ENSESTT00000036401 Transcript intron_variant - - - - - - rs7614761 3:10543438 C 491 NM_001683.3 Transcript intron_variant - - - - - - rs7614761 3:10543438 C 491 NM_001001331.2 Transcript intron_variant - - - - - - rs13089348 3:10688922 G - - - intergenic_variant - - - - - - rs4234505 3:10890281 G - ENSR00001357240 RegulatoryFeature regulatory_region_variant - - - - - - rs4234505 3:10890281 G 6538 NM_014229.1 Transcript intron_variant - - - - - - rs4234505 3:10890281 G ENSESTG00000014511 ENSESTT00000036357 Transcript downstream_gene_variant - - - - - - DISTANCE=4282 rs4234505 3:10890281 G CCDS2602.1 CCDS2602.1 Transcript intron_variant - - - - - - rs2655276 3:10925646 T - ENSR00001357245 RegulatoryFeature regulatory_region_variant - - - - - - rs2655276 3:10925646 T 6538 NM_014229.1 Transcript intron_variant - - - - - - rs2655276 3:10925646 T CCDS2602.1 CCDS2602.1 Transcript intron_variant - - - - - - rs2655276 3:10925646 T ENSESTG00000014526 ENSESTT00000036385 Transcript intron_variant - - - - - - rs2581214 3:10925664 C - ENSR00001357245 RegulatoryFeature regulatory_region_variant - - - - - - rs2581214 3:10925664 C 6538 NM_014229.1 Transcript intron_variant - - - - - - rs2581214 3:10925664 C CCDS2602.1 CCDS2602.1 Transcript intron_variant - - - - - - rs2581214 3:10925664 C ENSESTG00000014526 ENSESTT00000036385 Transcript intron_variant - - - - - - rs2629125 3:10949563 A 6538 NM_014229.1 Transcript intron_variant - - - - - - rs2629125 3:10949563 A ENSESTG00000009924 ENSESTT00000024821 Transcript upstream_gene_variant - - - - - - DISTANCE=4246 rs2629125 3:10949563 A CCDS2602.1 CCDS2602.1 Transcript intron_variant - - - - - - rs2629125 3:10949563 A ENSESTG00000014526 ENSESTT00000036385 Transcript intron_variant - - - - - - rs2655289 3:10989075 T - - - intergenic_variant - - - - - - rs2928088 3:11007147 C - - - intergenic_variant - - - - - - rs2930137 3:11035710 G 6529 NM_003042.3 Transcript intron_variant - - - - - - rs2930137 3:11035710 G ENSESTG00000009941 ENSESTT00000024880 Transcript intron_variant - - - - - - rs2930137 3:11035710 G ENSESTG00000009941 ENSESTT00000024875 Transcript intron_variant - - - - - - rs2944365 3:11047452 A - ENSR00001357266 RegulatoryFeature regulatory_region_variant - - - - - - rs2944365 3:11047452 A 6529 NM_003042.3 Transcript intron_variant - - - - - - rs2944365 3:11047452 A 100874090 NR_046647.1 Transcript downstream_gene_variant - - - - - - DISTANCE=332 rs2944365 3:11047452 A ENSESTG00000009941 ENSESTT00000024880 Transcript intron_variant - - - - - - rs2944365 3:11047452 A ENSESTG00000009941 ENSESTT00000024875 Transcript intron_variant - - - - - - rs2933302 3:11101184 C - ENSR00001357274 RegulatoryFeature regulatory_region_variant - - - - - - rs2933302 3:11101184 C - - - intergenic_variant - - - - - - rs2944369 3:11106158 G - - - intergenic_variant - - - - - - rs2944370 3:11110656 T - ENSR00001357278 RegulatoryFeature regulatory_region_variant - - - - - - rs2944370 3:11110656 T - - - intergenic_variant - - - - - - rs2944362 3:11119464 A - ENSR00001357281 RegulatoryFeature regulatory_region_variant - - - - - - rs2944362 3:11119464 A - - - intergenic_variant - - - - - - rs2594987 3:11334423 G ENSESTG00000010016 ENSESTT00000025131 Transcript intron_variant - - - - - - rs2594987 3:11334423 G ENSESTG00000010016 ENSESTT00000025126 Transcript intron_variant - - - - - - rs2594987 3:11334423 G ENSESTG00000010016 ENSESTT00000025120 Transcript intron_variant - - - - - - rs2594987 3:11334423 G 10533 NM_001136031.2 Transcript intron_variant - - - - - - rs2594987 3:11334423 G ENSESTG00000010016 ENSESTT00000025141 Transcript intron_variant - - - - - - rs2594987 3:11334423 G ENSESTG00000010016 ENSESTT00000025122 Transcript intron_variant - - - - - - rs2594987 3:11334423 G ENSESTG00000010016 ENSESTT00000025136 Transcript intron_variant - - - - - - rs2594987 3:11334423 G 10533 NM_001144912.1 Transcript intron_variant - - - - - - rs2594987 3:11334423 G ENSESTG00000010016 ENSESTT00000025143 Transcript intron_variant - - - - - - rs2594987 3:11334423 G 10533 NM_006395.2 Transcript intron_variant - - - - - - rs2606754 3:11358949 T CCDS46753.1 CCDS46753.1 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025126 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025120 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025174 Transcript downstream_gene_variant - - - - - - DISTANCE=4079 rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025159 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025150 Transcript intron_variant - - - - - - rs2606754 3:11358949 T 10533 NM_001136031.2 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025162 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025148 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025141 Transcript downstream_gene_variant - - - - - - DISTANCE=4146 rs2606754 3:11358949 T CCDS46752.1 CCDS46752.1 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025168 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025131 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025153 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025165 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025146 Transcript intron_variant - - - - - - rs2606754 3:11358949 T CCDS2605.1 CCDS2605.1 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025122 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025136 Transcript downstream_gene_variant - - - - - - DISTANCE=4146 rs2606754 3:11358949 T 10533 NM_001144912.1 Transcript intron_variant - - - - - - rs2606754 3:11358949 T 10533 NM_006395.2 Transcript intron_variant - - - - - - rs2606754 3:11358949 T ENSESTG00000010016 ENSESTT00000025143 Transcript downstream_gene_variant - - - - - - DISTANCE=4146 rs892938 3:11596897 G CCDS46753.1 CCDS46753.1 Transcript downstream_gene_variant - - - - - - DISTANCE=580 rs892938 3:11596897 G 9686 NM_001128221.1 Transcript downstream_gene_variant - - - - - - DISTANCE=647 rs892938 3:11596897 G CCDS46756.1 CCDS46756.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3133 rs892938 3:11596897 G ENSESTG00000010016 ENSESTT00000025120 Transcript downstream_gene_variant - - - - - - DISTANCE=342 rs892938 3:11596897 G ENSESTG00000010207 ENSESTT00000025541 Transcript downstream_gene_variant - - - - - - DISTANCE=647 rs892938 3:11596897 G ENSESTG00000010016 ENSESTT00000025159 Transcript downstream_gene_variant - - - - - - DISTANCE=342 rs892938 3:11596897 G 10533 NM_001136031.2 Transcript 3_prime_UTR_variant 2728 - - - - - rs892938 3:11596897 G ENSESTG00000010016 ENSESTT00000025196 Transcript downstream_gene_variant - - - - - - DISTANCE=342 rs892938 3:11596897 G ENSESTG00000010207 ENSESTT00000025555 Transcript downstream_gene_variant - - - - - - DISTANCE=3212 rs892938 3:11596897 G CCDS2606.1 CCDS2606.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3133 rs892938 3:11596897 G 9686 NM_014667.2 Transcript downstream_gene_variant - - - - - - DISTANCE=647 rs892938 3:11596897 G CCDS46754.1 CCDS46754.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3133 rs892938 3:11596897 G ENSESTG00000010016 ENSESTT00000025181 Transcript downstream_gene_variant - - - - - - DISTANCE=342 rs892938 3:11596897 G ENSESTG00000010207 ENSESTT00000025539 Transcript downstream_gene_variant - - - - - - DISTANCE=3066 rs892938 3:11596897 G ENSESTG00000010207 ENSESTT00000025528 Transcript downstream_gene_variant - - - - - - DISTANCE=3066 rs892938 3:11596897 G CCDS46752.1 CCDS46752.1 Transcript downstream_gene_variant - - - - - - DISTANCE=580 rs892938 3:11596897 G ENSESTG00000010207 ENSESTT00000025549 Transcript downstream_gene_variant - - - - - - DISTANCE=3066 rs892938 3:11596897 G ENSESTG00000010016 ENSESTT00000025146 Transcript downstream_gene_variant - - - - - - DISTANCE=342 rs892938 3:11596897 G ENSESTG00000010016 ENSESTT00000025208 Transcript downstream_gene_variant - - - - - - DISTANCE=342 rs892938 3:11596897 G ENSESTG00000010207 ENSESTT00000025536 Transcript downstream_gene_variant - - - - - - DISTANCE=3066 rs892938 3:11596897 G CCDS2605.1 CCDS2605.1 Transcript downstream_gene_variant - - - - - - DISTANCE=580 rs892938 3:11596897 G 9686 NM_001128220.1 Transcript downstream_gene_variant - - - - - - DISTANCE=647 rs892938 3:11596897 G CCDS46755.1 CCDS46755.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3133 rs892938 3:11596897 G 9686 NM_001128219.1 Transcript downstream_gene_variant - - - - - - DISTANCE=647 rs892938 3:11596897 G 10533 NM_001144912.1 Transcript 3_prime_UTR_variant 2569 - - - - - rs892938 3:11596897 G 10533 NM_006395.2 Transcript 3_prime_UTR_variant 2809 - - - - - rs56072092 3:11622364 G ENSESTG00000010207 ENSESTT00000025549 Transcript intron_variant - - - - - - rs56072092 3:11622364 G ENSESTG00000010207 ENSESTT00000025541 Transcript intron_variant - - - - - - rs56072092 3:11622364 G ENSESTG00000010207 ENSESTT00000025536 Transcript intron_variant - - - - - - rs56072092 3:11622364 G ENSESTG00000010207 ENSESTT00000025555 Transcript intron_variant - - - - - - rs56072092 3:11622364 G CCDS2606.1 CCDS2606.1 Transcript intron_variant - - - - - - rs56072092 3:11622364 G 9686 NM_001128220.1 Transcript intron_variant - - - - - - rs56072092 3:11622364 G 9686 NM_014667.2 Transcript intron_variant - - - - - - rs56072092 3:11622364 G CCDS46755.1 CCDS46755.1 Transcript intron_variant - - - - - - rs56072092 3:11622364 G CCDS46754.1 CCDS46754.1 Transcript intron_variant - - - - - - rs56072092 3:11622364 G 9686 NM_001128219.1 Transcript intron_variant - - - - - - rs56072092 3:11622364 G ENSESTG00000010207 ENSESTT00000025528 Transcript intron_variant - - - - - - rs56072092 3:11622364 G ENSESTG00000010207 ENSESTT00000025539 Transcript intron_variant - - - - - - rs2574705 3:11701705 T CCDS2606.1 CCDS2606.1 Transcript intron_variant - - - - - - rs2574705 3:11701705 T 9686 NM_014667.2 Transcript intron_variant - - - - - - rs2574705 3:11701705 T ENSESTG00000010207 ENSESTT00000025536 Transcript intron_variant - - - - - - rs2574705 3:11701705 T ENSESTG00000010207 ENSESTT00000025528 Transcript intron_variant - - - - - - rs9849283 3:11756691 T 9686 NM_014667.2 Transcript intron_variant - - - - - - rs9849283 3:11756691 T ENSESTG00000010207 ENSESTT00000025536 Transcript intron_variant - - - - - - rs9849283 3:11756691 T ENSESTG00000010102 ENSESTT00000025287 Transcript upstream_gene_variant - - - - - - DISTANCE=4224 rs9849283 3:11756691 T ENSESTG00000010207 ENSESTT00000025528 Transcript intron_variant - - - - - - rs9310397 3:11897829 C - - - intergenic_variant - - - - - - rs2470576 3:11933184 T - - - intergenic_variant - - - - - - rs2935918 3:11933457 T - - - intergenic_variant - - - - - - rs2454152 3:11943222 G - - - intergenic_variant - - - - - - rs2470570 3:11964201 C - - - intergenic_variant - - - - - - rs2470569 3:11982275 A - - - intergenic_variant - - - - - - rs2443737 3:11982296 A - - - intergenic_variant - - - - - - rs2443738 3:11982316 A - - - intergenic_variant - - - - - - rs62241790 3:11984994 T - - - intergenic_variant - - - - - - rs2618399 3:12044037 C - - - intergenic_variant - - - - - - rs2618397 3:12045157 G - - - intergenic_variant - - - - - - rs4530506 3:12255880 C - - - intergenic_variant - - - - - - rs2439740 3:12274806 A - - - intergenic_variant - - - - - - rs1797895 3:12447814 G - ENSR00001476631 RegulatoryFeature regulatory_region_variant - - - - - - rs1797895 3:12447814 G 5468 NM_005037.5 Transcript intron_variant - - - - - - rs1797895 3:12447814 G ENSESTG00000003030 ENSESTT00000007563 Transcript intron_variant - - - - - - rs1797895 3:12447814 G 5468 NM_138712.3 Transcript intron_variant - - - - - - rs1797895 3:12447814 G ENSESTG00000003022 ENSESTT00000007528 Transcript downstream_gene_variant - - - - - - DISTANCE=324 rs1797895 3:12447814 G 5468 NM_015869.4 Transcript intron_variant - - - - - - rs1797895 3:12447814 G CCDS2610.2 CCDS2610.2 Transcript intron_variant - - - - - - rs1797895 3:12447814 G CCDS2609.1 CCDS2609.1 Transcript intron_variant - - - - - - rs1797895 3:12447814 G ENSESTG00000003022 ENSESTT00000007540 Transcript downstream_gene_variant - - - - - - DISTANCE=324 rs1797895 3:12447814 G 5468 NM_138711.3 Transcript intron_variant - - - - - - rs2450858 3:12510992 A - - - intergenic_variant - - - - - - rs2655263 3:12538779 T CCDS2611.1 CCDS2611.1 Transcript intron_variant - - - - - - rs2655263 3:12538779 T ENSESTG00000003047 ENSESTT00000007647 Transcript intron_variant - - - - - - rs2655263 3:12538779 T CCDS46758.1 CCDS46758.1 Transcript intron_variant - - - - - - rs2655263 3:12538779 T 80746 NM_001145393.1 Transcript intron_variant - - - - - - rs2655263 3:12538779 T 80746 NM_001145394.1 Transcript intron_variant - - - - - - rs2655263 3:12538779 T CCDS46759.1 CCDS46759.1 Transcript intron_variant - - - - - - rs2655263 3:12538779 T CCDS46757.1 CCDS46757.1 Transcript intron_variant - - - - - - rs2655263 3:12538779 T 80746 NM_001145395.1 Transcript intron_variant - - - - - - rs2655263 3:12538779 T 80746 NM_025265.3 Transcript intron_variant - - - - - - rs2655263 3:12538779 T 80746 NM_001145392.1 Transcript intron_variant - - - - - - rs2454440 3:12650482 A - ENSR00001357624 RegulatoryFeature regulatory_region_variant - - - - - - rs2454440 3:12650482 A CCDS2612.1 CCDS2612.1 Transcript intron_variant - - - - - - rs2454440 3:12650482 A ENSESTG00000003162 ENSESTT00000007948 Transcript intron_variant - - - - - - rs2454440 3:12650482 A ENSESTG00000003162 ENSESTT00000007942 Transcript intron_variant - - - - - - rs2454440 3:12650482 A ENSESTG00000003162 ENSESTT00000007951 Transcript intron_variant - - - - - - rs2454440 3:12650482 A ENSESTG00000003162 ENSESTT00000007935 Transcript intron_variant - - - - - - rs2454440 3:12650482 A ENSESTG00000003162 ENSESTT00000007950 Transcript intron_variant - - - - - - rs2454440 3:12650482 A ENSESTG00000003162 ENSESTT00000007941 Transcript intron_variant - - - - - - rs2454440 3:12650482 A ENSESTG00000003162 ENSESTT00000007934 Transcript intron_variant - - - - - - rs2454440 3:12650482 A 5894 NM_002880.3 Transcript intron_variant - - - - - - rs2454440 3:12650482 A ENSESTG00000003162 ENSESTT00000007954 Transcript intron_variant - - - - - - rs9809226 3:12692338 G ENSESTG00000003162 ENSESTT00000007948 Transcript intron_variant - - - - - - rs9809226 3:12692338 G ENSESTG00000003162 ENSESTT00000007942 Transcript intron_variant - - - - - - rs9809226 3:12692338 G ENSESTG00000003162 ENSESTT00000007951 Transcript intron_variant - - - - - - rs9809226 3:12692338 G ENSESTG00000003162 ENSESTT00000007935 Transcript intron_variant - - - - - - rs9809226 3:12692338 G ENSESTG00000003162 ENSESTT00000007950 Transcript intron_variant - - - - - - rs9809226 3:12692338 G ENSESTG00000003162 ENSESTT00000007941 Transcript intron_variant - - - - - - rs9809226 3:12692338 G ENSESTG00000003162 ENSESTT00000007934 Transcript intron_variant - - - - - - rs9809226 3:12692338 G 5894 NM_002880.3 Transcript intron_variant - - - - - - rs9809226 3:12692338 G ENSESTG00000003162 ENSESTT00000007954 Transcript intron_variant - - - - - - rs7635425 3:12713448 A - - - intergenic_variant - - - - - - rs2594363 3:13247186 C - - - intergenic_variant - - - - - - rs357150 3:13256652 G - - - intergenic_variant - - - - - - rs4541388 3:13724870 C 285375 NR_027103.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4541388 3:13724870 C ENSESTG00000034226 ENSESTT00000086534 Transcript intron_variant - - - - - - rs4684990 3:13750176 T 285375 NR_027103.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4684990 3:13750176 T ENSESTG00000034226 ENSESTT00000086534 Transcript intron_variant - - - - - - rs2974385 3:13789906 G 285375 NR_027103.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1774 rs2974385 3:13789906 G ENSESTG00000034226 ENSESTT00000086534 Transcript downstream_gene_variant - - - - - - DISTANCE=1780 rs4685027 3:13835927 C - - - intergenic_variant - - - - - - rs9828293 3:13935136 T - - - intergenic_variant - - - - - - rs6773180 3:13977703 C 348825 NR_002223.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1104 rs6773180 3:13977703 C 100132526 NR_036481.1 Transcript non_coding_exon_variant,nc_transcript_variant 2636 - - - - - rs13085502 3:13997482 C 348825 NR_002223.3 Transcript intron_variant,nc_transcript_variant - - - - - - rs1350345 3:14085726 T 348825 NR_002223.3 Transcript intron_variant,nc_transcript_variant - - - - - - rs1870132 3:14094350 G 348825 NR_002223.3 Transcript intron_variant,nc_transcript_variant - - - - - - rs1870133 3:14094360 T 348825 NR_002223.3 Transcript intron_variant,nc_transcript_variant - - - - - - rs2045445 3:14149306 T 131474 NM_001098502.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4271 rs2045445 3:14149306 T 131474 NM_144636.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4271 rs2045445 3:14149306 T ENSESTG00000015544 ENSESTT00000038975 Transcript downstream_gene_variant - - - - - - DISTANCE=4272 rs2045445 3:14149306 T ENSESTG00000015544 ENSESTT00000038970 Transcript downstream_gene_variant - - - - - - DISTANCE=4819 rs2045445 3:14149306 T ENSESTG00000015544 ENSESTT00000038940 Transcript downstream_gene_variant - - - - - - DISTANCE=4991 rs2958057 3:14197987 T - ENSR00001358071 RegulatoryFeature regulatory_region_variant - - - - - - rs2958057 3:14197987 T CCDS46764.1 CCDS46764.1 Transcript synonymous_variant 1770 1770 590 A gcT/gcA - rs2958057 3:14197987 T 7508 NR_027299.1 Transcript non_coding_exon_variant,nc_transcript_variant 1861 - - - - - rs2958057 3:14197987 T ENSESTG00000015494 ENSESTT00000038842 Transcript downstream_gene_variant - - - - - - DISTANCE=3305 rs2958057 3:14197987 T CCDS46763.1 CCDS46763.1 Transcript synonymous_variant 1881 1881 627 A gcT/gcA - rs2958057 3:14197987 T ENSESTG00000015521 ENSESTT00000038899 Transcript upstream_gene_variant - - - - - - DISTANCE=59 rs2958057 3:14197987 T 7508 NM_004628.4 Transcript synonymous_variant 1985 1881 627 A gcT/gcA - rs2958057 3:14197987 T 7508 NM_001145769.1 Transcript synonymous_variant 1874 1770 590 A gcT/gcA - rs6763964 3:14260558 A - - - intergenic_variant - - - - - - rs11928073 3:14296450 G - - - intergenic_variant - - - - - - rs11920494 3:14296599 G - - - intergenic_variant - - - - - - rs9882836 3:14376975 G - - - intergenic_variant - - - - - - rs4234530 3:14882186 A ENSESTG00000015472 ENSESTT00000038738 Transcript intron_variant - - - - - - rs4234530 3:14882186 A CCDS46767.1 CCDS46767.1 Transcript intron_variant - - - - - - rs4234530 3:14882186 A 152273 NM_152536.3 Transcript intron_variant - - - - - - rs4234531 3:14882390 A ENSESTG00000015472 ENSESTT00000038738 Transcript intron_variant - - - - - - rs4234531 3:14882390 A CCDS46767.1 CCDS46767.1 Transcript intron_variant - - - - - - rs4234531 3:14882390 A 152273 NM_152536.3 Transcript intron_variant - - - - - - rs4685237 3:15070374 C ENSESTG00000018589 ENSESTT00000046890 Transcript intron_variant - - - - - - rs4685237 3:15070374 C 7182 NM_003298.3 Transcript intron_variant - - - - - - rs4685237 3:15070374 C ENSESTG00000018589 ENSESTT00000046883 Transcript intron_variant - - - - - - rs4685237 3:15070374 C ENSESTG00000018589 ENSESTT00000046899 Transcript intron_variant - - - - - - rs4685237 3:15070374 C ENSESTG00000018589 ENSESTT00000046905 Transcript downstream_gene_variant - - - - - - DISTANCE=22 rs4685237 3:15070374 C CCDS2621.1 CCDS2621.1 Transcript intron_variant - - - - - - rs540600 3:15096472 G ENSESTG00000011412 ENSESTT00000028667 Transcript intron_variant - - - - - - rs540600 3:15096472 G 64432 NM_022497.3 Transcript intron_variant - - - - - - rs540600 3:15096472 G ENSESTG00000018589 ENSESTT00000046883 Transcript downstream_gene_variant - - - - - - DISTANCE=1489 rs540600 3:15096472 G CCDS2622.1 CCDS2622.1 Transcript intron_variant - - - - - - rs540600 3:15096472 G ENSESTG00000011412 ENSESTT00000028664 Transcript intron_variant - - - - - - rs2729686 3:15351810 G ENSESTG00000011383 ENSESTT00000028581 Transcript intron_variant - - - - - - rs2729686 3:15351810 G CCDS2625.2 CCDS2625.2 Transcript intron_variant - - - - - - rs2729686 3:15351810 G 9467 NM_001018009.3 Transcript intron_variant - - - - - - rs2729686 3:15351810 G 9467 NM_004844.4 Transcript intron_variant - - - - - - rs2729686 3:15351810 G ENSESTG00000011383 ENSESTT00000028604 Transcript intron_variant - - - - - - rs4599288 3:15543089 C 8292 NM_080539.3 Transcript intron_variant - - - - - - rs4599288 3:15543089 C ENSESTG00000011360 ENSESTT00000028534 Transcript upstream_gene_variant - - - - - - DISTANCE=2975 rs4599288 3:15543089 C 8292 NM_080538.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2710 rs4599288 3:15543089 C CCDS43057.1 CCDS43057.1 Transcript intron_variant - - - - - - rs4599288 3:15543089 C 8292 NM_005677.3 Transcript intron_variant - - - - - - rs4599288 3:15543089 C ENSESTG00000011360 ENSESTT00000028531 Transcript intron_variant - - - - - - rs4599288 3:15543089 C ENSESTG00000011360 ENSESTT00000028526 Transcript intron_variant - - - - - - rs4599288 3:15543089 C ENSESTG00000011360 ENSESTT00000028545 Transcript upstream_gene_variant - - - - - - DISTANCE=3034 rs4599288 3:15543089 C CCDS46768.1 CCDS46768.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2995 rs4599288 3:15543089 C CCDS33709.1 CCDS33709.1 Transcript intron_variant - - - - - - rs7624871 3:15543111 C 8292 NM_080539.3 Transcript intron_variant - - - - - - rs7624871 3:15543111 C ENSESTG00000011360 ENSESTT00000028534 Transcript upstream_gene_variant - - - - - - DISTANCE=2997 rs7624871 3:15543111 C 8292 NM_080538.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2732 rs7624871 3:15543111 C CCDS43057.1 CCDS43057.1 Transcript intron_variant - - - - - - rs7624871 3:15543111 C 8292 NM_005677.3 Transcript intron_variant - - - - - - rs7624871 3:15543111 C ENSESTG00000011360 ENSESTT00000028531 Transcript intron_variant - - - - - - rs7624871 3:15543111 C ENSESTG00000011360 ENSESTT00000028526 Transcript intron_variant - - - - - - rs7624871 3:15543111 C ENSESTG00000011360 ENSESTT00000028545 Transcript upstream_gene_variant - - - - - - DISTANCE=3056 rs7624871 3:15543111 C CCDS46768.1 CCDS46768.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3017 rs7624871 3:15543111 C CCDS33709.1 CCDS33709.1 Transcript intron_variant - - - - - - rs4684250 3:15563391 T - ENSR00001476910 RegulatoryFeature regulatory_region_variant - - - - - - rs4684250 3:15563391 T CCDS43057.1 CCDS43057.1 Transcript upstream_gene_variant - - - - - - DISTANCE=259 rs4684250 3:15563391 T ENSESTG00000011360 ENSESTT00000028531 Transcript upstream_gene_variant - - - - - - DISTANCE=174 rs4684250 3:15563391 T 8292 NM_005677.3 Transcript upstream_gene_variant - - - - - - DISTANCE=133 rs4684250 3:15563391 T ENSESTG00000011360 ENSESTT00000028526 Transcript upstream_gene_variant - - - - - - DISTANCE=114 rs4684250 3:15563391 T 8292 NM_080539.3 Transcript upstream_gene_variant - - - - - - DISTANCE=133 rs4684250 3:15563391 T CCDS33709.1 CCDS33709.1 Transcript upstream_gene_variant - - - - - - DISTANCE=259 rs6442580 3:16155115 C - - - intergenic_variant - - - - - - rs2730341 3:16182072 T - ENSR00001476972 RegulatoryFeature regulatory_region_variant - - - - - - rs2730341 3:16182072 T - - - intergenic_variant - - - - - - rs13071729 3:17000015 T 23228 NM_015184.5 Transcript intron_variant - - - - - - rs13071729 3:17000015 T ENSESTG00000008137 ENSESTT00000020550 Transcript intron_variant - - - - - - rs13071729 3:17000015 T 23228 NM_001144382.1 Transcript intron_variant - - - - - - rs4234540 3:17161210 T - - - intergenic_variant - - - - - - rs1446304 3:17482801 A 9779 NM_001134381.1 Transcript intron_variant - - - - - - rs1446304 3:17482801 A ENSESTG00000008173 ENSESTT00000020768 Transcript intron_variant - - - - - - rs1446304 3:17482801 A ENSESTG00000008173 ENSESTT00000020702 Transcript intron_variant - - - - - - rs1446304 3:17482801 A CCDS33714.1 CCDS33714.1 Transcript intron_variant - - - - - - rs1446304 3:17482801 A 9779 NM_014744.2 Transcript intron_variant - - - - - - rs1446304 3:17482801 A CCDS46770.1 CCDS46770.1 Transcript intron_variant - - - - - - rs1446304 3:17482801 A ENSESTG00000008173 ENSESTT00000020789 Transcript intron_variant - - - - - - rs1446304 3:17482801 A ENSESTG00000008173 ENSESTT00000020696 Transcript intron_variant - - - - - - rs1446304 3:17482801 A ENSESTG00000008173 ENSESTT00000020804 Transcript intron_variant - - - - - - rs1446304 3:17482801 A ENSESTG00000008173 ENSESTT00000020795 Transcript intron_variant - - - - - - rs1446304 3:17482801 A 9779 NM_001134380.1 Transcript intron_variant - - - - - - rs4373093 3:17708926 G ENSESTG00000008173 ENSESTT00000020781 Transcript intron_variant - - - - - - rs4373093 3:17708926 G 9779 NM_001134381.1 Transcript intron_variant - - - - - - rs4373093 3:17708926 G ENSESTG00000008173 ENSESTT00000020768 Transcript intron_variant - - - - - - rs4373093 3:17708926 G ENSESTG00000008173 ENSESTT00000020702 Transcript intron_variant - - - - - - rs4373093 3:17708926 G 9779 NM_014744.2 Transcript intron_variant - - - - - - rs4373093 3:17708926 G ENSESTG00000008173 ENSESTT00000020789 Transcript intron_variant - - - - - - rs4373093 3:17708926 G ENSESTG00000008173 ENSESTT00000020696 Transcript intron_variant - - - - - - rs4373093 3:17708926 G ENSESTG00000008173 ENSESTT00000020804 Transcript intron_variant - - - - - - rs4373093 3:17708926 G ENSESTG00000008173 ENSESTT00000020795 Transcript intron_variant - - - - - - rs4373093 3:17708926 G 9779 NM_001134380.1 Transcript intron_variant - - - - - - rs4373093 3:17708926 G ENSESTG00000008173 ENSESTT00000020656 Transcript intron_variant - - - - - - rs4373093 3:17708926 G ENSESTG00000008173 ENSESTT00000020666 Transcript intron_variant - - - - - - rs4401390 3:17723659 C ENSESTG00000008173 ENSESTT00000020781 Transcript intron_variant - - - - - - rs4401390 3:17723659 C 9779 NM_001134381.1 Transcript intron_variant - - - - - - rs4401390 3:17723659 C ENSESTG00000008173 ENSESTT00000020768 Transcript intron_variant - - - - - - rs4401390 3:17723659 C ENSESTG00000008173 ENSESTT00000020702 Transcript intron_variant - - - - - - rs4401390 3:17723659 C 9779 NM_014744.2 Transcript intron_variant - - - - - - rs4401390 3:17723659 C ENSESTG00000008173 ENSESTT00000020789 Transcript intron_variant - - - - - - rs4401390 3:17723659 C ENSESTG00000008173 ENSESTT00000020696 Transcript intron_variant - - - - - - rs4401390 3:17723659 C ENSESTG00000008173 ENSESTT00000020804 Transcript intron_variant - - - - - - rs4401390 3:17723659 C ENSESTG00000008173 ENSESTT00000020795 Transcript intron_variant - - - - - - rs4401390 3:17723659 C 9779 NM_001134380.1 Transcript intron_variant - - - - - - rs4401390 3:17723659 C ENSESTG00000008173 ENSESTT00000020656 Transcript intron_variant - - - - - - rs4401390 3:17723659 C ENSESTG00000008173 ENSESTT00000020666 Transcript intron_variant - - - - - - rs4337657 3:17764268 C ENSESTG00000008173 ENSESTT00000020781 Transcript intron_variant - - - - - - rs4337657 3:17764268 C ENSESTG00000008173 ENSESTT00000020768 Transcript intron_variant - - - - - - rs4337657 3:17764268 C ENSESTG00000008173 ENSESTT00000020702 Transcript intron_variant - - - - - - rs4337657 3:17764268 C 9779 NM_014744.2 Transcript intron_variant - - - - - - rs4337657 3:17764268 C ENSESTG00000008173 ENSESTT00000020789 Transcript intron_variant - - - - - - rs4337657 3:17764268 C ENSESTG00000008173 ENSESTT00000020696 Transcript intron_variant - - - - - - rs4337657 3:17764268 C 9779 NM_001134380.1 Transcript intron_variant - - - - - - rs4337657 3:17764268 C ENSESTG00000008173 ENSESTT00000020656 Transcript intron_variant - - - - - - rs4337657 3:17764268 C ENSESTG00000008173 ENSESTT00000020666 Transcript intron_variant - - - - - - rs11128905 3:18742333 G - - - intergenic_variant - - - - - - rs6551231 3:19391872 G 131096 NM_144633.2 Transcript intron_variant - - - - - - rs6551231 3:19391872 G CCDS2632.1 CCDS2632.1 Transcript intron_variant - - - - - - rs6551231 3:19391872 G ENSESTG00000010954 ENSESTT00000027467 Transcript intron_variant - - - - - - rs6551231 3:19391872 G ENSESTG00000010954 ENSESTT00000027471 Transcript downstream_gene_variant - - - - - - DISTANCE=2498 rs6551231 3:19391872 G ENSESTG00000010954 ENSESTT00000027474 Transcript intron_variant - - - - - - rs269371 3:19858002 T ENSESTG00000011037 ENSESTT00000027687 Transcript downstream_gene_variant - - - - - - DISTANCE=100 rs2929379 3:19942680 G ENSESTG00000026669 ENSESTT00000067183 Transcript intron_variant - - - - - - rs2929379 3:19942680 G CCDS33715.2 CCDS33715.2 Transcript intron_variant - - - - - - rs2929379 3:19942680 G 151651 NM_144715.3 Transcript intron_variant - - - - - - rs2929379 3:19942680 G ENSESTG00000011037 ENSESTT00000027687 Transcript intron_variant - - - - - - rs2929379 3:19942680 G ENSESTG00000026669 ENSESTT00000067203 Transcript intron_variant - - - - - - rs9864799 3:20164908 G ENSESTG00000026430 ENSESTT00000066888 Transcript intron_variant - - - - - - rs9864799 3:20164908 G 8850 NM_003884.4 Transcript intron_variant - - - - - - rs9864799 3:20164908 G ENSESTG00000026430 ENSESTT00000066887 Transcript intron_variant - - - - - - rs9864799 3:20164908 G ENSESTG00000026430 ENSESTT00000066854 Transcript intron_variant - - - - - - rs9864799 3:20164908 G CCDS2634.1 CCDS2634.1 Transcript intron_variant - - - - - - rs9864799 3:20164908 G ENSESTG00000026430 ENSESTT00000066864 Transcript intron_variant - - - - - - rs9837803 3:20974506 T - - - intergenic_variant - - - - - - rs7626807 3:21023759 C - - - intergenic_variant - - - - - - rs1497503 3:21173773 G - - - intergenic_variant - - - - - - rs779025 3:21931786 G 100505836 XM_003118873.2 Transcript intron_variant - - - - - - rs259426 3:22067409 T 100505836 XM_003118873.2 Transcript intron_variant - - - - - - rs2728994 3:22309579 G 100505836 XM_003118872.2 Transcript intron_variant - - - - - - rs2728994 3:22309579 G 100505836 XM_003118873.2 Transcript intron_variant - - - - - - rs1161976 3:22683246 C - - - intergenic_variant - - - - - - rs615454 3:22793130 A - - - intergenic_variant - - - - - - rs6550745 3:23247514 A 7325 NM_152653.3 Transcript intron_variant - - - - - - rs6550745 3:23247514 A ENSESTG00000033671 ENSESTT00000085129 Transcript intron_variant - - - - - - rs6550745 3:23247514 A CCDS2637.1 CCDS2637.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2677 rs6550745 3:23247514 A ENSESTG00000020692 ENSESTT00000051879 Transcript upstream_gene_variant - - - - - - DISTANCE=3523 rs6550745 3:23247514 A ENSESTG00000033671 ENSESTT00000085115 Transcript intron_variant - - - - - - rs6550745 3:23247514 A ENSESTG00000020692 ENSESTT00000051871 Transcript upstream_gene_variant - - - - - - DISTANCE=3478 rs7629032 3:23648656 A - - - intergenic_variant - - - - - - rs4491843 3:23715376 G - - - intergenic_variant - - - - - - rs4858097 3:24006477 A ENSESTG00000010350 ENSESTT00000025892 Transcript missense_variant 1320 1156 386 L/M Ttg/Atg - rs4858097 3:24006477 A ENSESTG00000010350 ENSESTT00000025893 Transcript downstream_gene_variant - - - - - - DISTANCE=2880 rs4858097 3:24006477 A 9975 NM_001145425.1 Transcript missense_variant 1273 931 311 L/M Ttg/Atg - rs4858097 3:24006477 A ENSESTG00000010361 ENSESTT00000025912 Transcript upstream_gene_variant - - - - - - DISTANCE=2852 rs4858097 3:24006477 A ENSESTG00000010350 ENSESTT00000025896 Transcript missense_variant 1273 931 311 L/M Ttg/Atg - rs4858097 3:24006477 A ENSESTG00000010350 ENSESTT00000025898 Transcript downstream_gene_variant - - - - - - DISTANCE=2880 rs4858097 3:24006477 A ENSESTG00000010350 ENSESTT00000025889 Transcript missense_variant 1293 1156 386 L/M Ttg/Atg - rs4858097 3:24006477 A CCDS33718.1 CCDS33718.1 Transcript missense_variant 1156 1156 386 L/M Ttg/Atg - PolyPhen=benign;SIFT=tolerated rs4858097 3:24006477 A 9975 NM_005126.4 Transcript missense_variant 1475 1156 386 L/M Ttg/Atg - PolyPhen=benign;SIFT=tolerated rs4858097 3:24006477 A ENSESTG00000010350 ENSESTT00000025891 Transcript downstream_gene_variant - - - - - - DISTANCE=2880 rs2683537 3:24218019 A ENSESTG00000010369 ENSESTT00000025938 Transcript intron_variant - - - - - - rs2683537 3:24218019 A ENSESTG00000010369 ENSESTT00000025940 Transcript intron_variant - - - - - - rs2683537 3:24218019 A 7068 NM_000461.4 Transcript intron_variant - - - - - - rs2683537 3:24218019 A ENSESTG00000010365 ENSESTT00000025919 Transcript intron_variant - - - - - - rs2683537 3:24218019 A CCDS2641.1 CCDS2641.1 Transcript intron_variant - - - - - - rs2683537 3:24218019 A 7068 NM_001128177.1 Transcript intron_variant - - - - - - rs2683537 3:24218019 A 7068 NM_001252634.1 Transcript intron_variant - - - - - - rs2683537 3:24218019 A 7068 NM_001128176.2 Transcript intron_variant - - - - - - rs4295122 3:24348197 G ENSESTG00000010369 ENSESTT00000025938 Transcript intron_variant - - - - - - rs4295122 3:24348197 G ENSESTG00000010369 ENSESTT00000025940 Transcript intron_variant - - - - - - rs4295122 3:24348197 G ENSESTG00000010369 ENSESTT00000025934 Transcript intron_variant - - - - - - rs4295122 3:24348197 G 7068 NM_001128176.2 Transcript intron_variant - - - - - - rs4295122 3:24348197 G 7068 NM_000461.4 Transcript intron_variant - - - - - - rs4295122 3:24348197 G 7068 NM_001128177.1 Transcript intron_variant - - - - - - rs4295122 3:24348197 G 7068 NM_001252634.1 Transcript intron_variant - - - - - - rs1910851 3:24418891 T - ENSR00001477409 RegulatoryFeature regulatory_region_variant - - - - - - rs1910851 3:24418891 T ENSESTG00000010369 ENSESTT00000025938 Transcript intron_variant - - - - - - rs1910851 3:24418891 T ENSESTG00000010369 ENSESTT00000025940 Transcript intron_variant - - - - - - rs1910851 3:24418891 T ENSESTG00000010369 ENSESTT00000025934 Transcript intron_variant - - - - - - rs1910851 3:24418891 T 7068 NM_001128176.2 Transcript intron_variant - - - - - - rs1910851 3:24418891 T 7068 NM_000461.4 Transcript intron_variant - - - - - - rs1910851 3:24418891 T 7068 NM_001128177.1 Transcript intron_variant - - - - - - rs1910851 3:24418891 T 7068 NM_001252634.1 Transcript intron_variant - - - - - - rs2117871 3:24559309 G 100616448 NR_039955.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3544 rs9876737 3:24821043 T - - - intergenic_variant - - - - - - rs1286774 3:25702088 A 7155 NM_001068.2 Transcript intron_variant - - - - - - rs1286774 3:25702088 A ENSESTG00000031338 ENSESTT00000079162 Transcript intron_variant - - - - - - rs1286774 3:25702088 A ENSESTG00000031338 ENSESTT00000079133 Transcript intron_variant - - - - - - rs1286774 3:25702088 A CCDS46776.1 CCDS46776.1 Transcript intron_variant - - - - - - rs1286774 3:25702088 A ENSESTG00000031338 ENSESTT00000079180 Transcript intron_variant - - - - - - rs1286774 3:25702088 A 100616477 NR_039644.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4276 rs6551029 3:26099490 G - - - intergenic_variant - - - - - - rs1875575 3:26448032 A - - - intergenic_variant - - - - - - rs1907161 3:26581589 A - - - intergenic_variant - - - - - - rs6791144 3:26682573 G ENSESTG00000019072 ENSESTT00000047965 Transcript intron_variant - - - - - - rs6791144 3:26682573 G 116135 NM_052953.2 Transcript intron_variant - - - - - - rs6791144 3:26682573 G ENSESTG00000019072 ENSESTT00000047976 Transcript intron_variant - - - - - - rs6791144 3:26682573 G ENSESTG00000019072 ENSESTT00000047949 Transcript intron_variant - - - - - - rs7652051 3:26688282 G ENSESTG00000019072 ENSESTT00000047965 Transcript intron_variant - - - - - - rs7652051 3:26688282 G 116135 NM_052953.2 Transcript intron_variant - - - - - - rs7652051 3:26688282 G ENSESTG00000019072 ENSESTT00000047976 Transcript intron_variant - - - - - - rs7652051 3:26688282 G ENSESTG00000019072 ENSESTT00000047949 Transcript intron_variant - - - - - - rs4470468 3:26712367 C ENSESTG00000019072 ENSESTT00000047965 Transcript intron_variant - - - - - - rs4470468 3:26712367 C 116135 NM_052953.2 Transcript intron_variant - - - - - - rs4470468 3:26712367 C ENSESTG00000019072 ENSESTT00000047976 Transcript intron_variant - - - - - - rs4470468 3:26712367 C ENSESTG00000019072 ENSESTT00000047949 Transcript intron_variant - - - - - - rs1586711 3:26720926 G ENSESTG00000019072 ENSESTT00000047965 Transcript intron_variant - - - - - - rs1586711 3:26720926 G 116135 NM_052953.2 Transcript intron_variant - - - - - - rs1586711 3:26720926 G ENSESTG00000019072 ENSESTT00000047976 Transcript intron_variant - - - - - - rs1586711 3:26720926 G ENSESTG00000019072 ENSESTT00000047949 Transcript intron_variant - - - - - - rs2724487 3:27686326 T - - - intergenic_variant - - - - - - rs4680739 3:27855882 A ENSESTG00000000348 ENSESTT00000000876 Transcript intron_variant - - - - - - rs4680749 3:28302310 C CCDS33722.1 CCDS33722.1 Transcript intron_variant - - - - - - rs4680749 3:28302310 C ENSESTG00000034974 ENSESTT00000088407 Transcript intron_variant - - - - - - rs4680749 3:28302310 C ENSESTG00000034974 ENSESTT00000088404 Transcript intron_variant - - - - - - rs4680749 3:28302310 C ENSESTG00000034974 ENSESTT00000088392 Transcript intron_variant - - - - - - rs4680749 3:28302310 C 152100 NM_182523.1 Transcript intron_variant - - - - - - rs1350398 3:28503594 G 152098 NM_001040432.1 Transcript intron_variant - - - - - - rs1350398 3:28503594 G CCDS33723.1 CCDS33723.1 Transcript intron_variant - - - - - - rs1350398 3:28503594 G ENSESTG00000034985 ENSESTT00000088421 Transcript intron_variant - - - - - - rs9823799 3:28807425 A - - - intergenic_variant - - - - - - rs2053222 3:29254535 A - - - intergenic_variant - - - - - - rs9874961 3:30339424 A - - - intergenic_variant - - - - - - rs903609 3:30456409 G - - - intergenic_variant - - - - - - rs9879955 3:30491700 A - - - intergenic_variant - - - - - - rs79856262 3:31507267 T - - - intergenic_variant - - - - - - rs4955139 3:32354005 C CCDS2652.1 CCDS2652.1 Transcript intron_variant - - - - - - rs4955139 3:32354005 C ENSESTG00000011886 ENSESTT00000029765 Transcript intron_variant - - - - - - rs4955139 3:32354005 C 152189 NM_178868.3 Transcript intron_variant - - - - - - rs6550144 3:32702445 G - - - intergenic_variant - - - - - - rs499109 3:33541985 G ENSESTG00000021338 ENSESTT00000053614 Transcript intron_variant - - - - - - rs499109 3:33541985 G 23122 NM_015097.2 Transcript intron_variant - - - - - - rs499109 3:33541985 G ENSESTG00000021338 ENSESTT00000053620 Transcript intron_variant - - - - - - rs499109 3:33541985 G 23122 NM_001207044.1 Transcript intron_variant - - - - - - rs2049338 3:33555911 T ENSESTG00000021338 ENSESTT00000053614 Transcript intron_variant - - - - - - rs2049338 3:33555911 T 23122 NM_015097.2 Transcript intron_variant - - - - - - rs2049338 3:33555911 T ENSESTG00000021338 ENSESTT00000053620 Transcript intron_variant - - - - - - rs2049338 3:33555911 T 23122 NM_001207044.1 Transcript intron_variant - - - - - - rs6550233 3:33864751 C ENSESTG00000012647 ENSESTT00000031711 Transcript downstream_gene_variant - - - - - - DISTANCE=3754 rs6550233 3:33864751 C 10015 NM_001162429.2 Transcript intron_variant - - - - - - rs6550233 3:33864751 C 10015 NM_013374.5 Transcript intron_variant - - - - - - rs6550233 3:33864751 C 10015 NM_001256192.1 Transcript intron_variant - - - - - - rs6550233 3:33864751 C CCDS54561.1 CCDS54561.1 Transcript intron_variant - - - - - - rs6550233 3:33864751 C ENSESTG00000012558 ENSESTT00000031611 Transcript intron_variant - - - - - - rs6550233 3:33864751 C CCDS2660.1 CCDS2660.1 Transcript intron_variant - - - - - - rs1203760 3:34596791 T ENSESTG00000012642 ENSESTT00000031690 Transcript intron_variant - - - - - - rs7611070 3:35001353 T - - - intergenic_variant - - - - - - rs4577413 3:35240108 C - - - intergenic_variant - - - - - - rs814492 3:35483430 C - - - intergenic_variant - - - - - - rs2687777 3:35491934 G - - - intergenic_variant - - - - - - rs9850426 3:35580528 T - - - intergenic_variant - - - - - - rs6550378 3:36000163 T - - - intergenic_variant - - - - - - rs4234257 3:36703275 C - - - intergenic_variant - - - - - - rs9838909 3:36906194 T ENSESTG00000019594 ENSESTT00000049161 Transcript intron_variant - - - - - - rs9838909 3:36906194 T CCDS46789.2 CCDS46789.2 Transcript intron_variant - - - - - - rs9838909 3:36906194 T 9881 NM_014831.2 Transcript intron_variant - - - - - - rs6767437 3:36970458 T CCDS46789.2 CCDS46789.2 Transcript intron_variant - - - - - - rs6767437 3:36970458 T ENSESTG00000021123 ENSESTT00000053004 Transcript intron_variant - - - - - - rs6767437 3:36970458 T 9881 NM_014831.2 Transcript intron_variant - - - - - - rs6550476 3:37447782 G 339883 NM_178339.2 Transcript intron_variant - - - - - - rs6550476 3:37447782 G 339883 NM_178342.2 Transcript intron_variant - - - - - - rs155519 3:37490247 G CCDS2669.1 CCDS2669.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3619 rs155519 3:37490247 G 3680 NM_002207.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3566 rs155519 3:37490247 G ENSESTG00000020389 ENSESTT00000051197 Transcript upstream_gene_variant - - - - - - DISTANCE=3602 rs574184 3:37572160 T - ENSR00001361230 RegulatoryFeature regulatory_region_variant - - - - - - rs574184 3:37572160 T ENSESTG00000020529 ENSESTT00000051458 Transcript intron_variant - - - - - - rs574184 3:37572160 T CCDS2669.1 CCDS2669.1 Transcript intron_variant - - - - - - rs574184 3:37572160 T 3680 NM_002207.2 Transcript intron_variant - - - - - - rs7372318 3:38717643 A - - - intergenic_variant - - - - - - rs4234136 3:38841532 C - - - intergenic_variant - - - - - - rs893119 3:41725900 T - ENSR00001478517 RegulatoryFeature regulatory_region_variant - - - - - - rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065244 Transcript upstream_gene_variant - - - - - - DISTANCE=2747 rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065189 Transcript intron_variant - - - - - - rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065146 Transcript intron_variant - - - - - - rs893119 3:41725900 T 54986 NM_017886.2 Transcript intron_variant - - - - - - rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065225 Transcript intron_variant - - - - - - rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065227 Transcript intron_variant - - - - - - rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065203 Transcript intron_variant - - - - - - rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065237 Transcript upstream_gene_variant - - - - - - DISTANCE=2747 rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065128 Transcript intron_variant - - - - - - rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065240 Transcript upstream_gene_variant - - - - - - DISTANCE=2747 rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065112 Transcript intron_variant - - - - - - rs893119 3:41725900 T CCDS43071.1 CCDS43071.1 Transcript intron_variant - - - - - - rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065131 Transcript intron_variant - - - - - - rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065260 Transcript upstream_gene_variant - - - - - - DISTANCE=2747 rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065268 Transcript upstream_gene_variant - - - - - - DISTANCE=2754 rs893119 3:41725900 T ENSESTG00000025734 ENSESTT00000065194 Transcript intron_variant - - - - - - rs77328578 3:42660330 T ENSESTG00000034369 ENSESTT00000086929 Transcript upstream_gene_variant - - - - - - DISTANCE=2449 rs77328578 3:42660330 T ENSESTG00000034431 ENSESTT00000087088 Transcript intron_variant - - - - - - rs77328578 3:42660330 T ENSESTG00000034369 ENSESTT00000086911 Transcript intron_variant - - - - - - rs77328578 3:42660330 T 4820 NM_005385.3 Transcript intron_variant - - - - - - rs77328578 3:42660330 T CCDS2702.1 CCDS2702.1 Transcript intron_variant - - - - - - rs77328578 3:42660330 T ENSESTG00000034369 ENSESTT00000086920 Transcript intron_variant - - - - - - rs123508 3:42733831 G CCDS2703.1 CCDS2703.1 Transcript downstream_gene_variant - - - - - - DISTANCE=346 rs123508 3:42733831 G 131377 NM_152393.2 Transcript 3_prime_UTR_variant 2312 - - - - - rs123508 3:42733831 G 57467 NM_020707.3 Transcript downstream_gene_variant - - - - - - DISTANCE=324 rs123508 3:42733831 G 57467 NR_027753.1 Transcript downstream_gene_variant - - - - - - DISTANCE=324 rs123508 3:42733831 G CCDS2704.1 CCDS2704.1 Transcript downstream_gene_variant - - - - - - DISTANCE=412 rs123508 3:42733831 G ENSESTG00000034412 ENSESTT00000087054 Transcript 3_prime_UTR_variant 1113 - - - - - rs9758873 3:42977080 A CCDS54572.1 CCDS54572.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3308 rs9758873 3:42977080 A ENSESTG00000033807 ENSESTT00000085508 Transcript upstream_gene_variant - - - - - - DISTANCE=1271 rs9758873 3:42977080 A ENSESTG00000033807 ENSESTT00000085504 Transcript upstream_gene_variant - - - - - - DISTANCE=804 rs9758873 3:42977080 A ENSESTG00000033807 ENSESTT00000085481 Transcript upstream_gene_variant - - - - - - DISTANCE=774 rs9758873 3:42977080 A 100506243 NM_001205272.1 Transcript upstream_gene_variant - - - - - - DISTANCE=754 rs834184 3:43058967 G 729085 NM_001129908.2 Transcript intron_variant - - - - - - rs834184 3:43058967 G ENSESTG00000033807 ENSESTT00000085528 Transcript intron_variant - - - - - - rs834184 3:43058967 G CCDS46808.1 CCDS46808.1 Transcript intron_variant - - - - - - rs834184 3:43058967 G ENSESTG00000033807 ENSESTT00000085526 Transcript intron_variant - - - - - - rs834184 3:43058967 G ENSESTG00000033807 ENSESTT00000085521 Transcript intron_variant - - - - - - rs834184 3:43058967 G ENSESTG00000033807 ENSESTT00000085508 Transcript intron_variant - - - - - - rs834184 3:43058967 G ENSESTG00000033807 ENSESTT00000085481 Transcript intron_variant - - - - - - rs834184 3:43058967 G ENSESTG00000033807 ENSESTT00000085504 Transcript intron_variant - - - - - - rs9819446 3:43346885 T 54861 NM_001100594.1 Transcript intron_variant - - - - - - rs9819446 3:43346885 T 54861 NM_017719.4 Transcript intron_variant - - - - - - rs9819446 3:43346885 T ENSESTG00000033835 ENSESTT00000085565 Transcript downstream_gene_variant - - - - - - DISTANCE=1681 rs9819446 3:43346885 T CCDS43075.1 CCDS43075.1 Transcript intron_variant - - - - - - rs9819446 3:43346885 T ENSESTG00000033835 ENSESTT00000085559 Transcript downstream_gene_variant - - - - - - DISTANCE=1681 rs4356794 3:43505685 C ENSESTG00000033929 ENSESTT00000085766 Transcript intron_variant - - - - - - rs4356794 3:43505685 C 55129 NM_001204834.1 Transcript intron_variant - - - - - - rs4356794 3:43505685 C CCDS56250.1 CCDS56250.1 Transcript intron_variant - - - - - - rs4356794 3:43505685 C CCDS2710.2 CCDS2710.2 Transcript intron_variant - - - - - - rs4356794 3:43505685 C 55129 NM_001204833.1 Transcript intron_variant - - - - - - rs4356794 3:43505685 C CCDS56248.1 CCDS56248.1 Transcript intron_variant - - - - - - rs4356794 3:43505685 C 55129 NM_001204831.1 Transcript intron_variant - - - - - - rs4356794 3:43505685 C ENSESTG00000033929 ENSESTT00000085769 Transcript intron_variant - - - - - - rs4356794 3:43505685 C CCDS56249.1 CCDS56249.1 Transcript intron_variant - - - - - - rs4356794 3:43505685 C CCDS56247.1 CCDS56247.1 Transcript intron_variant - - - - - - rs4356794 3:43505685 C 55129 NM_001204832.1 Transcript intron_variant - - - - - - rs4356794 3:43505685 C 55129 NM_018075.3 Transcript intron_variant - - - - - - rs7614702 3:44753052 T ENSESTG00000022958 ENSESTT00000057966 Transcript upstream_gene_variant - - - - - - DISTANCE=1132 rs7614702 3:44753052 T 91392 NM_001134441.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1083 rs7614702 3:44753052 T 91392 NM_001134442.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1083 rs7614702 3:44753052 T 91392 NM_033210.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1083 rs7614702 3:44753052 T ENSESTG00000022958 ENSESTT00000057948 Transcript upstream_gene_variant - - - - - - DISTANCE=1093 rs7614702 3:44753052 T 91392 NM_001134440.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1083 rs1905148 3:45545875 C 23395 NM_015340.3 Transcript intron_variant - - - - - - rs1905148 3:45545875 C 100885795 NR_048543.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1905148 3:45545875 C CCDS2728.1 CCDS2728.1 Transcript intron_variant - - - - - - rs1905148 3:45545875 C ENSESTG00000026173 ENSESTT00000066195 Transcript intron_variant - - - - - - rs4682792 3:45679401 T ENSESTG00000026397 ENSESTT00000066579 Transcript intron_variant - - - - - - rs4682792 3:45679401 T ENSESTG00000026397 ENSESTT00000066565 Transcript intron_variant - - - - - - rs4682792 3:45679401 T CCDS2729.1 CCDS2729.1 Transcript intron_variant - - - - - - rs4682792 3:45679401 T 8994 NM_014240.2 Transcript intron_variant - - - - - - rs4593065 3:45684664 G - ENSR00001478774 RegulatoryFeature regulatory_region_variant - - - - - - rs4593065 3:45684664 G ENSESTG00000026397 ENSESTT00000066579 Transcript intron_variant - - - - - - rs4593065 3:45684664 G ENSESTG00000026397 ENSESTT00000066565 Transcript intron_variant - - - - - - rs4593065 3:45684664 G CCDS2729.1 CCDS2729.1 Transcript intron_variant - - - - - - rs4593065 3:45684664 G 8994 NM_014240.2 Transcript intron_variant - - - - - - rs4583695 3:45687693 G ENSESTG00000026397 ENSESTT00000066579 Transcript intron_variant - - - - - - rs4583695 3:45687693 G ENSESTG00000026397 ENSESTT00000066565 Transcript intron_variant - - - - - - rs4583695 3:45687693 G CCDS2729.1 CCDS2729.1 Transcript intron_variant - - - - - - rs4583695 3:45687693 G 8994 NM_014240.2 Transcript intron_variant - - - - - - rs9839290 3:45696762 C ENSESTG00000026397 ENSESTT00000066579 Transcript intron_variant - - - - - - rs9839290 3:45696762 C ENSESTG00000026397 ENSESTT00000066565 Transcript intron_variant - - - - - - rs9839290 3:45696762 C CCDS2729.1 CCDS2729.1 Transcript intron_variant - - - - - - rs9839290 3:45696762 C 8994 NM_014240.2 Transcript intron_variant - - - - - - rs1873002 3:45977899 C CCDS2734.1 CCDS2734.1 Transcript intron_variant - - - - - - rs1873002 3:45977899 C ENSESTG00000015572 ENSESTT00000039027 Transcript intron_variant - - - - - - rs1873002 3:45977899 C 79443 NM_024513.3 Transcript intron_variant - - - - - - rs1873002 3:45977899 C ENSESTG00000015572 ENSESTT00000039023 Transcript intron_variant - - - - - - rs1873002 3:45977899 C ENSESTG00000015572 ENSESTT00000039005 Transcript intron_variant - - - - - - rs7652158 3:46042488 G - - - intergenic_variant - - - - - - rs904635 3:46106801 A - ENSR00001362861 RegulatoryFeature regulatory_region_variant - - - - - - rs904635 3:46106801 A - - - intergenic_variant - - - - - - rs4858832 3:47575048 C - ENSR00001478924 RegulatoryFeature regulatory_region_variant - - - - - - rs4858832 3:47575048 C - - - intergenic_variant - - - - - - rs11711075 3:47968731 A CCDS46818.1 CCDS46818.1 Transcript intron_variant - - - - - - rs11711075 3:47968731 A ENSESTG00000015777 ENSESTT00000039618 Transcript intron_variant - - - - - - rs11711075 3:47968731 A CCDS33750.1 CCDS33750.1 Transcript intron_variant - - - - - - rs11711075 3:47968731 A ENSESTG00000015777 ENSESTT00000039571 Transcript intron_variant - - - - - - rs11711075 3:47968731 A 4134 NM_001134364.1 Transcript intron_variant - - - - - - rs11711075 3:47968731 A 4134 NM_002375.4 Transcript intron_variant - - - - - - rs2351469 3:48013819 T CCDS46821.1 CCDS46821.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3129 rs2351469 3:48013819 T CCDS46818.1 CCDS46818.1 Transcript intron_variant - - - - - - rs2351469 3:48013819 T ENSESTG00000015777 ENSESTT00000039618 Transcript intron_variant - - - - - - rs2351469 3:48013819 T CCDS33750.1 CCDS33750.1 Transcript intron_variant - - - - - - rs2351469 3:48013819 T ENSESTG00000015777 ENSESTT00000039603 Transcript downstream_gene_variant - - - - - - DISTANCE=2673 rs2351469 3:48013819 T ENSESTG00000015777 ENSESTT00000039571 Transcript intron_variant - - - - - - rs2351469 3:48013819 T ENSESTG00000015777 ENSESTT00000039611 Transcript downstream_gene_variant - - - - - - DISTANCE=2991 rs2351469 3:48013819 T 4134 NM_030885.3 Transcript downstream_gene_variant - - - - - - DISTANCE=750 rs2351469 3:48013819 T 4134 NM_002375.4 Transcript intron_variant - - - - - - rs2351469 3:48013819 T 4134 NM_001134364.1 Transcript intron_variant - - - - - - rs1264193 3:48702336 A - ENSR00001363502 RegulatoryFeature regulatory_region_variant - - - - - - rs1264193 3:48702336 A ENSESTG00000015292 ENSESTT00000038294 Transcript intron_variant - - - - - - rs1264193 3:48702336 A 1951 NM_001407.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1988 rs1264193 3:48702336 A ENSESTG00000015283 ENSESTT00000038277 Transcript intron_variant - - - - - - rs1264193 3:48702336 A CCDS2775.1 CCDS2775.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2269 rs6442132 3:48818317 C CCDS2778.1 CCDS2778.1 Transcript intron_variant - - - - - - rs6442132 3:48818317 C ENSESTG00000011499 ENSESTT00000028912 Transcript intron_variant - - - - - - rs6442132 3:48818317 C 5576 NM_004157.2 Transcript intron_variant - - - - - - rs6442132 3:48818317 C ENSESTG00000011499 ENSESTT00000028908 Transcript intron_variant - - - - - - rs6804360 3:49265203 C 339834 NM_001135197.1 Transcript intron_variant - - - - - - rs6804360 3:49265203 C 339834 NM_178173.3 Transcript intron_variant - - - - - - rs6804360 3:49265203 C CCDS33755.2 CCDS33755.2 Transcript intron_variant - - - - - - rs6804360 3:49265203 C ENSESTG00000010759 ENSESTT00000026920 Transcript intron_variant - - - - - - rs6804360 3:49265203 C ENSESTG00000010759 ENSESTT00000026918 Transcript intron_variant - - - - - - rs6446299 3:49861049 G 10293 NM_005879.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4979 rs7433231 3:49928691 C CCDS2807.1 CCDS2807.1 Transcript missense_variant 3583 3583 1195 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs7433231 3:49928691 C CCDS58833.1 CCDS58833.1 Transcript missense_variant 3436 3436 1146 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs7433231 3:49928691 C ENSESTG00000013410 ENSESTT00000033577 Transcript missense_variant 470 220 74 S/G Agc/Ggc - rs7433231 3:49928691 C ENSESTG00000012844 ENSESTT00000032217 Transcript 3_prime_UTR_variant 431 - - - - - rs7433231 3:49928691 C 4486 NM_002447.2 Transcript missense_variant 3847 3583 1195 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs7433231 3:49928691 C 4486 NM_001244937.1 Transcript missense_variant 3700 3436 1146 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs762896 3:50428794 C 9254 NM_001005505.1 Transcript intron_variant - - - - - - rs762896 3:50428794 C 9254 NM_001174051.1 Transcript intron_variant - - - - - - rs762896 3:50428794 C CCDS54588.1 CCDS54588.1 Transcript intron_variant - - - - - - rs762896 3:50428794 C CCDS33763.1 CCDS33763.1 Transcript intron_variant - - - - - - rs762896 3:50428794 C 9254 NM_006030.2 Transcript intron_variant - - - - - - rs387474 3:50571505 G ENSESTG00000013314 ENSESTT00000033380 Transcript downstream_gene_variant - - - - - - DISTANCE=3573 rs441392 3:50585088 G ENSESTG00000013314 ENSESTT00000033380 Transcript upstream_gene_variant - - - - - - DISTANCE=4515 rs380436 3:50616685 G ENSESTG00000013291 ENSESTT00000033322 Transcript intron_variant - - - - - - rs380436 3:50616685 G ENSESTG00000013240 ENSESTT00000033215 Transcript upstream_gene_variant - - - - - - DISTANCE=638 rs380436 3:50616685 G CCDS2830.1 CCDS2830.1 Transcript intron_variant - - - - - - rs380436 3:50616685 G 51409 NM_016173.3 Transcript intron_variant - - - - - - rs414731 3:50623347 T 51409 NM_016173.3 Transcript downstream_gene_variant - - - - - - DISTANCE=925 rs1872185 3:50715342 C 1795 NM_004947.4 Transcript intron_variant - - - - - - rs1872185 3:50715342 C 100616138 NR_039950.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2748 rs1872185 3:50715342 C CCDS46835.1 CCDS46835.1 Transcript intron_variant - - - - - - rs11921421 3:50733657 G 1795 NM_004947.4 Transcript intron_variant - - - - - - rs11921421 3:50733657 G CCDS46835.1 CCDS46835.1 Transcript intron_variant - - - - - - rs7629929 3:50988635 T ENSESTG00000024839 ENSESTT00000062855 Transcript intron_variant - - - - - - rs7629929 3:50988635 T 1795 NM_004947.4 Transcript intron_variant - - - - - - rs7629929 3:50988635 T ENSESTG00000024839 ENSESTT00000062915 Transcript intron_variant - - - - - - rs7629929 3:50988635 T CCDS46835.1 CCDS46835.1 Transcript intron_variant - - - - - - rs9839729 3:51042205 G ENSESTG00000024839 ENSESTT00000062855 Transcript intron_variant - - - - - - rs9839729 3:51042205 G 1795 NM_004947.4 Transcript intron_variant - - - - - - rs9839729 3:51042205 G ENSESTG00000024839 ENSESTT00000062915 Transcript intron_variant - - - - - - rs9839729 3:51042205 G CCDS46835.1 CCDS46835.1 Transcript intron_variant - - - - - - rs4927968 3:51202712 C ENSESTG00000024839 ENSESTT00000062931 Transcript downstream_gene_variant - - - - - - DISTANCE=4510 rs4927968 3:51202712 C ENSESTG00000024839 ENSESTT00000062855 Transcript intron_variant - - - - - - rs4927968 3:51202712 C 1795 NM_004947.4 Transcript intron_variant - - - - - - rs4927968 3:51202712 C CCDS46835.1 CCDS46835.1 Transcript intron_variant - - - - - - rs6445813 3:51625500 A - ENSR00001479138 RegulatoryFeature regulatory_region_variant - - - - - - rs6445813 3:51625500 A CCDS33765.2 CCDS33765.2 Transcript intron_variant - - - - - - rs6445813 3:51625500 A ENSESTG00000025055 ENSESTT00000063563 Transcript intron_variant - - - - - - rs6445813 3:51625500 A 23132 NM_015106.2 Transcript intron_variant - - - - - - rs6445813 3:51625500 A ENSESTG00000025055 ENSESTT00000063573 Transcript intron_variant - - - - - - rs6445813 3:51625500 A ENSESTG00000025055 ENSESTT00000063591 Transcript intron_variant - - - - - - rs6445813 3:51625500 A ENSESTG00000025055 ENSESTT00000063280 Transcript intron_variant - - - - - - rs6445813 3:51625500 A ENSESTG00000025055 ENSESTT00000063595 Transcript intron_variant - - - - - - rs6445813 3:51625500 A ENSESTG00000025055 ENSESTT00000063622 Transcript intron_variant - - - - - - rs6445813 3:51625500 A ENSESTG00000025055 ENSESTT00000063335 Transcript intron_variant - - - - - - rs1603606 3:51775139 C - - - intergenic_variant - - - - - - rs7643375 3:51780467 G - - - intergenic_variant - - - - - - rs186551 3:51950655 A - - - intergenic_variant - - - - - - rs696652 3:52347223 G ENSESTG00000026400 ENSESTT00000066511 Transcript upstream_gene_variant - - - - - - DISTANCE=3292 rs696652 3:52347223 G ENSESTG00000026412 ENSESTT00000066539 Transcript upstream_gene_variant - - - - - - DISTANCE=4664 rs696652 3:52347223 G 25981 NM_015512.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3112 rs770284 3:52415865 G CCDS46842.1 CCDS46842.1 Transcript intron_variant - - - - - - rs770284 3:52415865 G ENSESTG00000026565 ENSESTT00000066862 Transcript upstream_gene_variant - - - - - - DISTANCE=4950 rs770284 3:52415865 G 25981 NM_015512.4 Transcript intron_variant - - - - - - rs770284 3:52415865 G ENSESTG00000026503 ENSESTT00000066840 Transcript intron_variant - - - - - - rs6445497 3:52524480 T - ENSR00001364266 RegulatoryFeature regulatory_region_variant - - - - - - rs6445497 3:52524480 T ENSESTG00000026959 ENSESTT00000068051 Transcript upstream_gene_variant - - - - - - DISTANCE=4905 rs6445497 3:52524480 T ENSESTG00000026917 ENSESTT00000067830 Transcript intron_variant - - - - - - rs6445497 3:52524480 T CCDS33767.1 CCDS33767.1 Transcript intron_variant - - - - - - rs6445497 3:52524480 T ENSESTG00000026959 ENSESTT00000068039 Transcript upstream_gene_variant - - - - - - DISTANCE=4874 rs6445497 3:52524480 T ENSESTG00000026761 ENSESTT00000067769 Transcript downstream_gene_variant - - - - - - DISTANCE=2100 rs6445497 3:52524480 T 23166 NM_015136.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4876 rs6445497 3:52524480 T ENSESTG00000026917 ENSESTT00000067881 Transcript intron_variant - - - - - - rs6445497 3:52524480 T ENSESTG00000026761 ENSESTT00000067799 Transcript downstream_gene_variant - - - - - - DISTANCE=2100 rs6445497 3:52524480 T ENSESTG00000026917 ENSESTT00000067919 Transcript intron_variant - - - - - - rs6445497 3:52524480 T CCDS33768.1 CCDS33768.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4950 rs6445497 3:52524480 T 11188 NM_007184.3 Transcript intron_variant - - - - - - rs7620907 3:52853340 C CCDS54596.1 CCDS54596.1 Transcript intron_variant - - - - - - rs7620907 3:52853340 C 3700 NM_002218.4 Transcript intron_variant - - - - - - rs7620907 3:52853340 C 3700 NM_001166449.1 Transcript intron_variant - - - - - - rs7620907 3:52853340 C CCDS2865.1 CCDS2865.1 Transcript intron_variant - - - - - - rs7620907 3:52853340 C ENSESTG00000032249 ENSESTT00000081395 Transcript upstream_gene_variant - - - - - - DISTANCE=4639 rs2564945 3:53044701 T 51460 NM_016329.3 Transcript intron_variant - - - - - - rs2564959 3:53133776 G ENSESTG00000032476 ENSESTT00000082023 Transcript intron_variant - - - - - - rs2564959 3:53133776 G CCDS2869.1 CCDS2869.1 Transcript intron_variant - - - - - - rs2564959 3:53133776 G ENSESTG00000032476 ENSESTT00000082031 Transcript intron_variant - - - - - - rs2564959 3:53133776 G ENSESTG00000032476 ENSESTT00000082051 Transcript intron_variant - - - - - - rs2564959 3:53133776 G 91869 NM_052859.3 Transcript intron_variant - - - - - - rs6764214 3:53304880 C - ENSR00001364451 RegulatoryFeature regulatory_region_variant - - - - - - rs6764214 3:53304880 C - - - intergenic_variant - - - - - - rs9877441 3:53901580 C 93973 NM_022899.4 Transcript 3_prime_UTR_variant 3142 - - - - - rs9877441 3:53901580 C ENSESTG00000014110 ENSESTT00000035280 Transcript downstream_gene_variant - - - - - - DISTANCE=3842 rs9877441 3:53901580 C CCDS2874.1 CCDS2874.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2245 rs9877441 3:53901580 C 55540 NM_018725.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1753 rs9877441 3:53901580 C ENSESTG00000014110 ENSESTT00000035288 Transcript downstream_gene_variant - - - - - - DISTANCE=3919 rs9877441 3:53901580 C CCDS2875.1 CCDS2875.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1166 rs6445658 3:54454479 A ENSESTG00000014055 ENSESTT00000035185 Transcript intron_variant - - - - - - rs6445658 3:54454479 A ENSESTG00000014055 ENSESTT00000035175 Transcript intron_variant - - - - - - rs6445658 3:54454479 A 55799 NM_018398.2 Transcript intron_variant - - - - - - rs6445658 3:54454479 A ENSESTG00000014055 ENSESTT00000035182 Transcript intron_variant - - - - - - rs6445658 3:54454479 A CCDS54598.1 CCDS54598.1 Transcript intron_variant - - - - - - rs6445658 3:54454479 A ENSESTG00000014055 ENSESTT00000035168 Transcript intron_variant - - - - - - rs6445658 3:54454479 A ENSESTG00000014055 ENSESTT00000035147 Transcript intron_variant - - - - - - rs6414579 3:54517830 A ENSESTG00000014055 ENSESTT00000035185 Transcript intron_variant - - - - - - rs6414579 3:54517830 A ENSESTG00000014055 ENSESTT00000035175 Transcript intron_variant - - - - - - rs6414579 3:54517830 A 55799 NM_018398.2 Transcript intron_variant - - - - - - rs6414579 3:54517830 A ENSESTG00000014055 ENSESTT00000035182 Transcript intron_variant - - - - - - rs6414579 3:54517830 A CCDS54598.1 CCDS54598.1 Transcript intron_variant - - - - - - rs6414579 3:54517830 A ENSESTG00000014055 ENSESTT00000035168 Transcript intron_variant - - - - - - rs6414579 3:54517830 A ENSESTG00000014055 ENSESTT00000035147 Transcript intron_variant - - - - - - rs6445695 3:54580505 C ENSESTG00000014055 ENSESTT00000035185 Transcript intron_variant - - - - - - rs6445695 3:54580505 C ENSESTG00000014055 ENSESTT00000035175 Transcript intron_variant - - - - - - rs6445695 3:54580505 C 55799 NM_018398.2 Transcript intron_variant - - - - - - rs6445695 3:54580505 C ENSESTG00000014055 ENSESTT00000035182 Transcript intron_variant - - - - - - rs6445695 3:54580505 C CCDS54598.1 CCDS54598.1 Transcript intron_variant - - - - - - rs6445695 3:54580505 C ENSESTG00000014055 ENSESTT00000035168 Transcript intron_variant - - - - - - rs6445695 3:54580505 C ENSESTG00000014055 ENSESTT00000035147 Transcript intron_variant - - - - - - rs6445699 3:54585252 G ENSESTG00000014055 ENSESTT00000035185 Transcript intron_variant - - - - - - rs6445699 3:54585252 G ENSESTG00000014055 ENSESTT00000035175 Transcript intron_variant - - - - - - rs6445699 3:54585252 G 55799 NM_018398.2 Transcript intron_variant - - - - - - rs6445699 3:54585252 G ENSESTG00000014055 ENSESTT00000035182 Transcript intron_variant - - - - - - rs6445699 3:54585252 G CCDS54598.1 CCDS54598.1 Transcript intron_variant - - - - - - rs6445699 3:54585252 G ENSESTG00000014055 ENSESTT00000035168 Transcript intron_variant - - - - - - rs6445699 3:54585252 G ENSESTG00000014055 ENSESTT00000035147 Transcript intron_variant - - - - - - rs615219 3:54706220 A ENSESTG00000014055 ENSESTT00000035185 Transcript intron_variant - - - - - - rs615219 3:54706220 A ENSESTG00000014055 ENSESTT00000035194 Transcript intron_variant - - - - - - rs615219 3:54706220 A 55799 NM_018398.2 Transcript intron_variant - - - - - - rs615219 3:54706220 A CCDS54598.1 CCDS54598.1 Transcript intron_variant - - - - - - rs615219 3:54706220 A ENSESTG00000014055 ENSESTT00000035168 Transcript intron_variant - - - - - - rs615219 3:54706220 A ENSESTG00000014055 ENSESTT00000035147 Transcript intron_variant - - - - - - rs838029 3:54744805 A ENSESTG00000014055 ENSESTT00000035185 Transcript intron_variant - - - - - - rs838029 3:54744805 A 55799 NM_018398.2 Transcript intron_variant - - - - - - rs838029 3:54744805 A CCDS54598.1 CCDS54598.1 Transcript intron_variant - - - - - - rs838029 3:54744805 A ENSESTG00000014055 ENSESTT00000035168 Transcript intron_variant - - - - - - rs838029 3:54744805 A ENSESTG00000014055 ENSESTT00000035147 Transcript intron_variant - - - - - - rs1969480 3:54911292 T ENSESTG00000016536 ENSESTT00000041608 Transcript intron_variant - - - - - - rs1969480 3:54911292 T ENSESTG00000016536 ENSESTT00000041557 Transcript intron_variant - - - - - - rs1969480 3:54911292 T ENSESTG00000016536 ENSESTT00000041479 Transcript intron_variant - - - - - - rs1969480 3:54911292 T 100874237 NR_046666.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1969480 3:54911292 T CCDS54598.1 CCDS54598.1 Transcript intron_variant - - - - - - rs1969480 3:54911292 T ENSESTG00000016536 ENSESTT00000041584 Transcript intron_variant - - - - - - rs1969480 3:54911292 T ENSESTG00000016536 ENSESTT00000041485 Transcript intron_variant - - - - - - rs1969480 3:54911292 T ENSESTG00000016536 ENSESTT00000041570 Transcript intron_variant - - - - - - rs1969480 3:54911292 T 55799 NM_018398.2 Transcript intron_variant - - - - - - rs1461797 3:55224064 T - - - intergenic_variant - - - - - - rs1466395 3:55241442 T - - - intergenic_variant - - - - - - rs401925 3:55253732 C - - - intergenic_variant - - - - - - rs617241 3:55253909 G - - - intergenic_variant - - - - - - rs427007 3:55256064 T - - - intergenic_variant - - - - - - rs422891 3:55275102 C - - - intergenic_variant - - - - - - rs358787 3:55279801 G - - - intergenic_variant - - - - - - rs358894 3:55300941 C - - - intergenic_variant - - - - - - rs181682 3:55343515 G - ENSR00001364730 RegulatoryFeature regulatory_region_variant - - - - - - rs181682 3:55343515 G - - - intergenic_variant - - - - - - rs358814 3:55344399 G - - - intergenic_variant - - - - - - rs1185611 3:55448664 A - - - intergenic_variant - - - - - - rs1696248 3:55623768 G ENSESTG00000016629 ENSESTT00000041708 Transcript intron_variant - - - - - - rs1696248 3:55623768 G ENSESTG00000016629 ENSESTT00000041688 Transcript intron_variant - - - - - - rs1696248 3:55623768 G 26059 NM_015576.1 Transcript intron_variant - - - - - - rs1696248 3:55623768 G ENSESTG00000016629 ENSESTT00000041701 Transcript intron_variant - - - - - - rs1152116 3:55685317 G ENSESTG00000016629 ENSESTT00000041688 Transcript intron_variant - - - - - - rs1152116 3:55685317 G 26059 NM_015576.1 Transcript intron_variant - - - - - - rs1152116 3:55685317 G ENSESTG00000016629 ENSESTT00000041697 Transcript intron_variant - - - - - - rs1152116 3:55685317 G ENSESTG00000016629 ENSESTT00000041701 Transcript upstream_gene_variant - - - - - - DISTANCE=4063 rs6797885 3:56410974 G CCDS46851.1 CCDS46851.1 Transcript intron_variant - - - - - - rs6797885 3:56410974 G 26059 NM_015576.1 Transcript intron_variant - - - - - - rs9868389 3:56797373 C CCDS46855.1 CCDS46855.1 Transcript intron_variant - - - - - - rs9868389 3:56797373 C ENSESTG00000006535 ENSESTT00000016519 Transcript intron_variant - - - - - - rs9868389 3:56797373 C CCDS2878.1 CCDS2878.1 Transcript intron_variant - - - - - - rs9868389 3:56797373 C 50650 NM_019555.2 Transcript intron_variant - - - - - - rs9868389 3:56797373 C CCDS46854.1 CCDS46854.1 Transcript intron_variant - - - - - - rs9868389 3:56797373 C ENSESTG00000006535 ENSESTT00000016521 Transcript intron_variant - - - - - - rs9868389 3:56797373 C ENSESTG00000006535 ENSESTT00000016522 Transcript intron_variant - - - - - - rs9868389 3:56797373 C ENSESTG00000006535 ENSESTT00000016511 Transcript intron_variant - - - - - - rs9868389 3:56797373 C 50650 NM_001128616.1 Transcript intron_variant - - - - - - rs9868389 3:56797373 C ENSESTG00000006535 ENSESTT00000016497 Transcript intron_variant - - - - - - rs9868389 3:56797373 C 50650 NM_001128615.1 Transcript intron_variant - - - - - - rs9868389 3:56797373 C ENSESTG00000006535 ENSESTT00000016479 Transcript intron_variant - - - - - - rs28394068 3:58496562 G ENSESTG00000033318 ENSESTT00000084191 Transcript intron_variant - - - - - - rs28394068 3:58496562 G 8309 NM_003500.3 Transcript intron_variant - - - - - - rs28394068 3:58496562 G CCDS33775.1 CCDS33775.1 Transcript intron_variant - - - - - - rs79663548 3:58767323 A ENSESTG00000030232 ENSESTT00000076087 Transcript intron_variant - - - - - - rs79663548 3:58767323 A ENSESTG00000033222 ENSESTT00000083907 Transcript intron_variant - - - - - - rs79663548 3:58767323 A CCDS33776.1 CCDS33776.1 Transcript intron_variant - - - - - - rs79663548 3:58767323 A ENSESTG00000030232 ENSESTT00000076136 Transcript intron_variant - - - - - - rs79663548 3:58767323 A 200844 NM_198463.2 Transcript intron_variant - - - - - - rs6414593 3:59282241 C - - - intergenic_variant - - - - - - rs7630648 3:59305526 A - - - intergenic_variant - - - - - - rs576299 3:59770612 C 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs576299 3:59770612 C ENSESTG00000030196 ENSESTT00000075982 Transcript intron_variant - - - - - - rs576299 3:59770612 C CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs576299 3:59770612 C 2272 NM_002012.2 Transcript intron_variant - - - - - - rs576299 3:59770612 C ENSESTG00000033783 ENSESTT00000085405 Transcript intron_variant - - - - - - rs576299 3:59770612 C ENSESTG00000033783 ENSESTT00000085411 Transcript intron_variant - - - - - - rs212056 3:60030428 C 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs212056 3:60030428 C CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs212056 3:60030428 C 2272 NM_002012.2 Transcript intron_variant - - - - - - rs212056 3:60030428 C ENSESTG00000033783 ENSESTT00000085398 Transcript intron_variant - - - - - - rs212056 3:60030428 C ENSESTG00000033783 ENSESTT00000085405 Transcript intron_variant - - - - - - rs1474524 3:60115747 G 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs1474524 3:60115747 G CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs1474524 3:60115747 G 2272 NM_002012.2 Transcript intron_variant - - - - - - rs213425 3:60173304 A 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs213425 3:60173304 A CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs213425 3:60173304 A 2272 NM_002012.2 Transcript intron_variant - - - - - - rs169916 3:60173314 A 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs169916 3:60173314 A CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs169916 3:60173314 A 2272 NM_002012.2 Transcript intron_variant - - - - - - rs213314 3:60191503 T 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs213314 3:60191503 T CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs213314 3:60191503 T 2272 NM_002012.2 Transcript intron_variant - - - - - - rs213393 3:60236910 T 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs213393 3:60236910 T CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs213393 3:60236910 T 2272 NM_002012.2 Transcript intron_variant - - - - - - rs125635 3:60275996 C 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs125635 3:60275996 C CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs125635 3:60275996 C 2272 NM_002012.2 Transcript intron_variant - - - - - - rs213378 3:60279108 A 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs213378 3:60279108 A CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs213378 3:60279108 A 2272 NM_002012.2 Transcript intron_variant - - - - - - rs213379 3:60291494 G 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs213379 3:60291494 G CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs213379 3:60291494 G 2272 NM_002012.2 Transcript intron_variant - - - - - - rs6446124 3:60330686 C 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs6446124 3:60330686 C CCDS2894.1 CCDS2894.1 Transcript intron_variant - - - - - - rs6446124 3:60330686 C 2272 NM_002012.2 Transcript intron_variant - - - - - - rs7629955 3:60855594 A 2272 NM_001166243.1 Transcript intron_variant - - - - - - rs7629955 3:60855594 A 2272 NM_002012.2 Transcript intron_variant - - - - - - rs6783654 3:62413875 T - ENSR00001365875 RegulatoryFeature regulatory_region_variant - - - - - - rs6783654 3:62413875 T CCDS2899.1 CCDS2899.1 Transcript intron_variant - - - - - - rs6783654 3:62413875 T ENSESTG00000023904 ENSESTT00000060766 Transcript intron_variant - - - - - - rs6783654 3:62413875 T ENSESTG00000023904 ENSESTT00000060711 Transcript intron_variant - - - - - - rs6783654 3:62413875 T ENSESTG00000023904 ENSESTT00000060606 Transcript intron_variant - - - - - - rs6783654 3:62413875 T 8618 NM_183393.2 Transcript intron_variant - - - - - - rs6783654 3:62413875 T CCDS2898.1 CCDS2898.1 Transcript intron_variant - - - - - - rs6783654 3:62413875 T ENSESTG00000023904 ENSESTT00000060566 Transcript intron_variant - - - - - - rs6783654 3:62413875 T ENSESTG00000023904 ENSESTT00000060734 Transcript intron_variant - - - - - - rs6783654 3:62413875 T ENSESTG00000023904 ENSESTT00000060715 Transcript intron_variant - - - - - - rs6783654 3:62413875 T ENSESTG00000023904 ENSESTT00000060574 Transcript intron_variant - - - - - - rs6783654 3:62413875 T 8618 NM_183394.2 Transcript intron_variant - - - - - - rs6783654 3:62413875 T 8618 NM_003716.3 Transcript intron_variant - - - - - - rs6783654 3:62413875 T CCDS46858.1 CCDS46858.1 Transcript intron_variant - - - - - - rs6783654 3:62413875 T ENSESTG00000023904 ENSESTT00000060621 Transcript intron_variant - - - - - - rs6799019 3:62430289 G CCDS2899.1 CCDS2899.1 Transcript intron_variant - - - - - - rs6799019 3:62430289 G ENSESTG00000023904 ENSESTT00000060766 Transcript intron_variant - - - - - - rs6799019 3:62430289 G ENSESTG00000023904 ENSESTT00000060711 Transcript intron_variant - - - - - - rs6799019 3:62430289 G ENSESTG00000023904 ENSESTT00000060606 Transcript intron_variant - - - - - - rs6799019 3:62430289 G 8618 NM_183393.2 Transcript intron_variant - - - - - - rs6799019 3:62430289 G CCDS2898.1 CCDS2898.1 Transcript intron_variant - - - - - - rs6799019 3:62430289 G ENSESTG00000023904 ENSESTT00000060566 Transcript intron_variant - - - - - - rs6799019 3:62430289 G ENSESTG00000023904 ENSESTT00000060734 Transcript intron_variant - - - - - - rs6799019 3:62430289 G ENSESTG00000023904 ENSESTT00000060715 Transcript intron_variant - - - - - - rs6799019 3:62430289 G ENSESTG00000023904 ENSESTT00000060574 Transcript intron_variant - - - - - - rs6799019 3:62430289 G 8618 NM_183394.2 Transcript intron_variant - - - - - - rs6799019 3:62430289 G 8618 NM_003716.3 Transcript intron_variant - - - - - - rs6799019 3:62430289 G CCDS46858.1 CCDS46858.1 Transcript intron_variant - - - - - - rs6799019 3:62430289 G ENSESTG00000023904 ENSESTT00000060621 Transcript intron_variant - - - - - - rs1529185 3:62445795 T CCDS2899.1 CCDS2899.1 Transcript intron_variant - - - - - - rs1529185 3:62445795 T ENSESTG00000023904 ENSESTT00000060766 Transcript intron_variant - - - - - - rs1529185 3:62445795 T ENSESTG00000023904 ENSESTT00000060711 Transcript intron_variant - - - - - - rs1529185 3:62445795 T ENSESTG00000023904 ENSESTT00000060606 Transcript intron_variant - - - - - - rs1529185 3:62445795 T 8618 NM_183393.2 Transcript intron_variant - - - - - - rs1529185 3:62445795 T CCDS2898.1 CCDS2898.1 Transcript intron_variant - - - - - - rs1529185 3:62445795 T ENSESTG00000023904 ENSESTT00000060566 Transcript intron_variant - - - - - - rs1529185 3:62445795 T ENSESTG00000023904 ENSESTT00000060734 Transcript intron_variant - - - - - - rs1529185 3:62445795 T ENSESTG00000023904 ENSESTT00000060715 Transcript intron_variant - - - - - - rs1529185 3:62445795 T ENSESTG00000023904 ENSESTT00000060574 Transcript intron_variant - - - - - - rs1529185 3:62445795 T 8618 NM_183394.2 Transcript intron_variant - - - - - - rs1529185 3:62445795 T 8618 NM_003716.3 Transcript intron_variant - - - - - - rs1529185 3:62445795 T CCDS46858.1 CCDS46858.1 Transcript intron_variant - - - - - - rs1529185 3:62445795 T ENSESTG00000023904 ENSESTT00000060621 Transcript intron_variant - - - - - - rs6801056 3:62983509 G - - - intergenic_variant - - - - - - rs1584303 3:63013979 T - - - intergenic_variant - - - - - - rs1466958 3:63497275 T ENSESTG00000029984 ENSESTT00000075446 Transcript intron_variant - - - - - - rs1466958 3:63497275 T CCDS46860.1 CCDS46860.1 Transcript intron_variant - - - - - - rs1466958 3:63497275 T 100874016 NR_046677.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1466958 3:63497275 T ENSESTG00000030080 ENSESTT00000075681 Transcript intron_variant - - - - - - rs1466958 3:63497275 T 132204 NM_001130003.1 Transcript intron_variant - - - - - - rs1466958 3:63497275 T ENSESTG00000029984 ENSESTT00000075465 Transcript intron_variant - - - - - - rs1466958 3:63497275 T ENSESTG00000029984 ENSESTT00000075546 Transcript intron_variant - - - - - - rs1466958 3:63497275 T 132204 NM_144642.4 Transcript intron_variant - - - - - - rs1466958 3:63497275 T CCDS46859.1 CCDS46859.1 Transcript intron_variant - - - - - - rs1466958 3:63497275 T ENSESTG00000029984 ENSESTT00000075576 Transcript intron_variant - - - - - - rs1466958 3:63497275 T ENSESTG00000029984 ENSESTT00000075562 Transcript intron_variant - - - - - - rs1873564 3:63797300 G ENSESTG00000000338 ENSESTT00000000864 Transcript intron_variant - - - - - - rs27651 3:64134048 T ENSESTG00000000319 ENSESTT00000000777 Transcript upstream_gene_variant - - - - - - DISTANCE=1442 rs27651 3:64134048 T ENSESTG00000000313 ENSESTT00000000775 Transcript intron_variant - - - - - - rs27651 3:64134048 T 166336 NM_198859.3 Transcript intron_variant - - - - - - rs27651 3:64134048 T CCDS2902.1 CCDS2902.1 Transcript intron_variant - - - - - - rs173859 3:64157021 C ENSESTG00000000313 ENSESTT00000000775 Transcript intron_variant - - - - - - rs173859 3:64157021 C 166336 NM_198859.3 Transcript intron_variant - - - - - - rs173859 3:64157021 C CCDS2902.1 CCDS2902.1 Transcript intron_variant - - - - - - rs697289 3:64211708 T ENSESTG00000000313 ENSESTT00000000775 Transcript intron_variant - - - - - - rs697289 3:64211708 T 166336 NM_198859.3 Transcript upstream_gene_variant - - - - - - DISTANCE=577 rs704413 3:64248448 C - ENSR00001366088 RegulatoryFeature regulatory_region_variant - - - - - - rs704413 3:64248448 C ENSESTG00000000313 ENSESTT00000000775 Transcript intron_variant - - - - - - rs9819964 3:64415593 C - - - intergenic_variant - - - - - - rs318727 3:64756545 C ENSESTG00000015455 ENSESTT00000038684 Transcript intron_variant - - - - - - rs318727 3:64756545 C 100507098 NR_038264.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs318727 3:64756545 C ENSESTG00000000294 ENSESTT00000000721 Transcript intron_variant - - - - - - rs318786 3:64782202 T - ENSR00001366168 RegulatoryFeature regulatory_region_variant - - - - - - rs318786 3:64782202 T ENSESTG00000015455 ENSESTT00000038684 Transcript intron_variant - - - - - - rs318786 3:64782202 T 100507098 NR_038264.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs318786 3:64782202 T ENSESTG00000000294 ENSESTT00000000721 Transcript intron_variant - - - - - - rs7645931 3:65397347 T ENSESTG00000015491 ENSESTT00000038801 Transcript intron_variant - - - - - - rs7645931 3:65397347 T CCDS33780.1 CCDS33780.1 Transcript intron_variant - - - - - - rs7645931 3:65397347 T 9223 NM_015520.1 Transcript intron_variant - - - - - - rs7645931 3:65397347 T ENSESTG00000015491 ENSESTT00000038794 Transcript intron_variant - - - - - - rs7645931 3:65397347 T 9223 NM_004742.2 Transcript intron_variant - - - - - - rs7645931 3:65397347 T 9223 NM_001033057.1 Transcript intron_variant - - - - - - rs7645931 3:65397347 T CCDS2904.1 CCDS2904.1 Transcript intron_variant - - - - - - rs7645931 3:65397347 T CCDS33781.1 CCDS33781.1 Transcript intron_variant - - - - - - rs7636096 3:65464625 A ENSESTG00000015468 ENSESTT00000038746 Transcript intron_variant - - - - - - rs7636096 3:65464625 A CCDS33780.1 CCDS33780.1 Transcript intron_variant - - - - - - rs7636096 3:65464625 A ENSESTG00000015468 ENSESTT00000038752 Transcript intron_variant - - - - - - rs7636096 3:65464625 A 9223 NM_015520.1 Transcript intron_variant - - - - - - rs7636096 3:65464625 A ENSESTG00000015468 ENSESTT00000038748 Transcript intron_variant - - - - - - rs7636096 3:65464625 A ENSESTG00000015468 ENSESTT00000038754 Transcript intron_variant - - - - - - rs7636096 3:65464625 A 9223 NM_004742.2 Transcript intron_variant - - - - - - rs7636096 3:65464625 A 9223 NM_001033057.1 Transcript intron_variant - - - - - - rs7636096 3:65464625 A CCDS2904.1 CCDS2904.1 Transcript intron_variant - - - - - - rs7636096 3:65464625 A CCDS33781.1 CCDS33781.1 Transcript intron_variant - - - - - - rs7612933 3:65506775 C ENSESTG00000015468 ENSESTT00000038746 Transcript intron_variant - - - - - - rs7612933 3:65506775 C CCDS33780.1 CCDS33780.1 Transcript intron_variant - - - - - - rs7612933 3:65506775 C ENSESTG00000015468 ENSESTT00000038752 Transcript intron_variant - - - - - - rs7612933 3:65506775 C 9223 NM_015520.1 Transcript intron_variant - - - - - - rs7612933 3:65506775 C ENSESTG00000015468 ENSESTT00000038748 Transcript intron_variant - - - - - - rs7612933 3:65506775 C ENSESTG00000015468 ENSESTT00000038754 Transcript intron_variant - - - - - - rs7612933 3:65506775 C 9223 NM_004742.2 Transcript intron_variant - - - - - - rs7612933 3:65506775 C 9223 NM_001033057.1 Transcript intron_variant - - - - - - rs7612933 3:65506775 C CCDS2904.1 CCDS2904.1 Transcript intron_variant - - - - - - rs7612933 3:65506775 C CCDS33781.1 CCDS33781.1 Transcript intron_variant - - - - - - rs264085 3:65747757 C - ENSR00001366304 RegulatoryFeature regulatory_region_variant - - - - - - rs264085 3:65747757 C CCDS2904.1 CCDS2904.1 Transcript intron_variant - - - - - - rs264085 3:65747757 C 9223 NM_001033057.1 Transcript intron_variant - - - - - - rs264085 3:65747757 C 9223 NM_004742.2 Transcript intron_variant - - - - - - rs264085 3:65747757 C CCDS33780.1 CCDS33780.1 Transcript intron_variant - - - - - - rs264085 3:65747757 C CCDS33781.1 CCDS33781.1 Transcript intron_variant - - - - - - rs264085 3:65747757 C 9223 NM_015520.1 Transcript intron_variant - - - - - - rs264120 3:65807679 G CCDS2904.1 CCDS2904.1 Transcript intron_variant - - - - - - rs264120 3:65807679 G 9223 NM_001033057.1 Transcript intron_variant - - - - - - rs264120 3:65807679 G 9223 NM_004742.2 Transcript intron_variant - - - - - - rs264120 3:65807679 G CCDS33780.1 CCDS33780.1 Transcript intron_variant - - - - - - rs264120 3:65807679 G CCDS33781.1 CCDS33781.1 Transcript intron_variant - - - - - - rs264120 3:65807679 G 9223 NM_015520.1 Transcript intron_variant - - - - - - rs264121 3:65808274 G CCDS2904.1 CCDS2904.1 Transcript intron_variant - - - - - - rs264121 3:65808274 G 9223 NM_001033057.1 Transcript intron_variant - - - - - - rs264121 3:65808274 G 9223 NM_004742.2 Transcript intron_variant - - - - - - rs264121 3:65808274 G CCDS33780.1 CCDS33780.1 Transcript intron_variant - - - - - - rs264121 3:65808274 G CCDS33781.1 CCDS33781.1 Transcript intron_variant - - - - - - rs264121 3:65808274 G 9223 NM_015520.1 Transcript intron_variant - - - - - - rs1367314 3:65968107 G CCDS2904.1 CCDS2904.1 Transcript intron_variant - - - - - - rs1367314 3:65968107 G 9223 NM_001033057.1 Transcript intron_variant - - - - - - rs1367314 3:65968107 G 9223 NM_004742.2 Transcript intron_variant - - - - - - rs1367314 3:65968107 G CCDS33780.1 CCDS33780.1 Transcript intron_variant - - - - - - rs1367314 3:65968107 G CCDS33781.1 CCDS33781.1 Transcript intron_variant - - - - - - rs1367314 3:65968107 G 9223 NM_015520.1 Transcript intron_variant - - - - - - rs12634354 3:65975102 G CCDS2904.1 CCDS2904.1 Transcript intron_variant - - - - - - rs12634354 3:65975102 G 9223 NM_001033057.1 Transcript intron_variant - - - - - - rs12634354 3:65975102 G 9223 NM_004742.2 Transcript intron_variant - - - - - - rs12634354 3:65975102 G CCDS33780.1 CCDS33780.1 Transcript intron_variant - - - - - - rs12634354 3:65975102 G CCDS33781.1 CCDS33781.1 Transcript intron_variant - - - - - - rs12634354 3:65975102 G 9223 NM_015520.1 Transcript intron_variant - - - - - - rs3845901 3:66507598 G - ENSR00001480232 RegulatoryFeature regulatory_region_variant - - - - - - rs3845901 3:66507598 G ENSESTG00000015505 ENSESTT00000038934 Transcript intron_variant - - - - - - rs3845901 3:66507598 G ENSESTG00000015505 ENSESTT00000038916 Transcript intron_variant - - - - - - rs3845901 3:66507598 G CCDS33783.1 CCDS33783.1 Transcript intron_variant - - - - - - rs3845901 3:66507598 G 26018 NM_015541.2 Transcript intron_variant - - - - - - rs3845901 3:66507598 G ENSESTG00000015505 ENSESTT00000038946 Transcript intron_variant - - - - - - rs3845901 3:66507598 G ENSESTG00000015505 ENSESTT00000038895 Transcript intron_variant - - - - - - rs3952591 3:66713216 A - - - intergenic_variant - - - - - - rs6549828 3:67271659 T 100422941 NR_036234.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4229 rs4575824 3:67275326 G 100422941 NR_036234.1 Transcript upstream_gene_variant - - - - - - DISTANCE=562 rs4485665 3:67275512 C 100422941 NR_036234.1 Transcript upstream_gene_variant - - - - - - DISTANCE=376 rs4856856 3:67427703 C ENSESTG00000019608 ENSESTT00000049365 Transcript intron_variant - - - - - - rs4856856 3:67427703 C 8801 NM_001177599.1 Transcript intron_variant - - - - - - rs4856856 3:67427703 C CCDS54605.1 CCDS54605.1 Transcript intron_variant - - - - - - rs4856856 3:67427703 C CCDS43104.1 CCDS43104.1 Transcript intron_variant - - - - - - rs4856856 3:67427703 C 8801 NM_003848.3 Transcript intron_variant - - - - - - rs4856856 3:67427703 C ENSESTG00000019608 ENSESTT00000049350 Transcript intron_variant - - - - - - rs12492257 3:67693212 C ENSESTG00000019608 ENSESTT00000049365 Transcript intron_variant - - - - - - rs12492257 3:67693212 C 8801 NM_001177599.1 Transcript intron_variant - - - - - - rs12492257 3:67693212 C CCDS54605.1 CCDS54605.1 Transcript intron_variant - - - - - - rs12492257 3:67693212 C CCDS43104.1 CCDS43104.1 Transcript intron_variant - - - - - - rs12492257 3:67693212 C 8801 NM_003848.3 Transcript intron_variant - - - - - - rs12492257 3:67693212 C ENSESTG00000019608 ENSESTT00000049350 Transcript intron_variant - - - - - - rs7612480 3:68027982 A - - - intergenic_variant - - - - - - rs9850789 3:68150227 G 407738 NM_001252216.1 Transcript intron_variant - - - - - - rs9850789 3:68150227 G CCDS54606.1 CCDS54606.1 Transcript intron_variant - - - - - - rs9850789 3:68150227 G 407738 NM_213609.3 Transcript intron_variant - - - - - - rs7642888 3:68236556 A 407738 NM_001252216.1 Transcript intron_variant - - - - - - rs7642888 3:68236556 A CCDS54606.1 CCDS54606.1 Transcript intron_variant - - - - - - rs7642888 3:68236556 A 407738 NM_213609.3 Transcript intron_variant - - - - - - rs6763888 3:68708418 G ENSESTG00000034217 ENSESTT00000086520 Transcript intron_variant - - - - - - rs4611827 3:68920210 G ENSESTG00000034353 ENSESTT00000086876 Transcript intron_variant - - - - - - rs4611827 3:68920210 G CCDS2907.1 CCDS2907.1 Transcript intron_variant - - - - - - rs4611827 3:68920210 G ENSESTG00000034353 ENSESTT00000086871 Transcript intron_variant - - - - - - rs4611827 3:68920210 G 151647 NM_001005527.2 Transcript intron_variant - - - - - - rs4611827 3:68920210 G 151647 NM_182522.4 Transcript intron_variant - - - - - - rs13090370 3:68980869 G ENSESTG00000034353 ENSESTT00000086876 Transcript intron_variant - - - - - - rs13090370 3:68980869 G ENSESTG00000034353 ENSESTT00000086871 Transcript intron_variant - - - - - - rs13090370 3:68980869 G 151647 NM_001005527.2 Transcript intron_variant - - - - - - rs13090370 3:68980869 G 151647 NM_182522.4 Transcript intron_variant - - - - - - rs6778957 3:69188245 G - - - intergenic_variant - - - - - - rs9310151 3:69471895 T ENSESTG00000034245 ENSESTT00000086591 Transcript intron_variant - - - - - - rs9310151 3:69471895 T ENSESTG00000034245 ENSESTT00000086593 Transcript intron_variant - - - - - - rs9310151 3:69471895 T ENSESTG00000034245 ENSESTT00000086585 Transcript intron_variant - - - - - - rs1427439 3:69721389 A - - - intergenic_variant - - - - - - rs1427435 3:69746635 T - - - intergenic_variant - - - - - - rs11713240 3:69800588 G CCDS43106.1 CCDS43106.1 Transcript intron_variant - - - - - - rs11713240 3:69800588 G ENSESTG00000029346 ENSESTT00000073861 Transcript intron_variant - - - - - - rs11713240 3:69800588 G 4286 NM_198159.2 Transcript intron_variant - - - - - - rs4241391 3:69804541 A - ENSR00001366829 RegulatoryFeature regulatory_region_variant - - - - - - rs4241391 3:69804541 A CCDS43106.1 CCDS43106.1 Transcript intron_variant - - - - - - rs4241391 3:69804541 A ENSESTG00000029346 ENSESTT00000073861 Transcript intron_variant - - - - - - rs4241391 3:69804541 A 4286 NM_198159.2 Transcript intron_variant - - - - - - rs1835417 3:69841194 T - ENSR00001366848 RegulatoryFeature regulatory_region_variant - - - - - - rs1835417 3:69841194 T CCDS43106.1 CCDS43106.1 Transcript intron_variant - - - - - - rs1835417 3:69841194 T ENSESTG00000029346 ENSESTT00000073861 Transcript intron_variant - - - - - - rs1835417 3:69841194 T 4286 NM_006722.2 Transcript intron_variant - - - - - - rs1835417 3:69841194 T 4286 NM_198159.2 Transcript intron_variant - - - - - - rs1835417 3:69841194 T 4286 NM_001184967.1 Transcript intron_variant - - - - - - rs9812463 3:69949333 G CCDS54607.1 CCDS54607.1 Transcript intron_variant - - - - - - rs9812463 3:69949333 G CCDS46865.1 CCDS46865.1 Transcript intron_variant - - - - - - rs9812463 3:69949333 G 4286 NM_198177.2 Transcript intron_variant - - - - - - rs9812463 3:69949333 G CCDS43106.1 CCDS43106.1 Transcript intron_variant - - - - - - rs9812463 3:69949333 G 4286 NM_006722.2 Transcript intron_variant - - - - - - rs9812463 3:69949333 G 4286 NM_198159.2 Transcript intron_variant - - - - - - rs9812463 3:69949333 G 4286 NM_001184967.1 Transcript intron_variant - - - - - - rs9816522 3:70195973 G - - - intergenic_variant - - - - - - rs7644064 3:70242083 T ENSESTG00000029439 ENSESTT00000074080 Transcript downstream_gene_variant - - - - - - DISTANCE=4166 rs7427227 3:70272686 C - - - intergenic_variant - - - - - - rs6549314 3:70313215 G - - - intergenic_variant - - - - - - rs6776983 3:70364278 G - - - intergenic_variant - - - - - - rs4464416 3:70547850 C - - - intergenic_variant - - - - - - rs4974295 3:70556066 T ENSESTG00000029426 ENSESTT00000074066 Transcript downstream_gene_variant - - - - - - DISTANCE=4080 rs6771808 3:70607992 C - - - intergenic_variant - - - - - - rs1388434 3:70613877 C - - - intergenic_variant - - - - - - rs12638971 3:70713921 G - - - intergenic_variant - - - - - - rs9851697 3:70797190 A - - - intergenic_variant - - - - - - rs2687198 3:70923672 G - - - intergenic_variant - - - - - - rs2704803 3:71360867 G - ENSR00001367076 RegulatoryFeature regulatory_region_variant - - - - - - rs2704803 3:71360867 G ENSESTG00000023521 ENSESTT00000059309 Transcript intron_variant - - - - - - rs2704803 3:71360867 G ENSESTG00000023521 ENSESTT00000059377 Transcript intron_variant - - - - - - rs2704803 3:71360867 G 27086 NM_001012505.1 Transcript intron_variant - - - - - - rs2704803 3:71360867 G ENSESTG00000023521 ENSESTT00000059288 Transcript intron_variant - - - - - - rs2704803 3:71360867 G 27086 NM_032682.5 Transcript intron_variant - - - - - - rs2704803 3:71360867 G 27086 NM_001244808.1 Transcript intron_variant - - - - - - rs2704803 3:71360867 G 27086 NM_001244816.1 Transcript intron_variant - - - - - - rs2704803 3:71360867 G 27086 NM_001244810.1 Transcript intron_variant - - - - - - rs1298316 3:71413164 T ENSESTG00000023521 ENSESTT00000059309 Transcript intron_variant - - - - - - rs1298316 3:71413164 T ENSESTG00000023521 ENSESTT00000059377 Transcript upstream_gene_variant - - - - - - DISTANCE=3244 rs1298316 3:71413164 T 27086 NM_001012505.1 Transcript intron_variant - - - - - - rs1298316 3:71413164 T ENSESTG00000023521 ENSESTT00000059347 Transcript intron_variant - - - - - - rs1298316 3:71413164 T ENSESTG00000023521 ENSESTT00000059288 Transcript intron_variant - - - - - - rs1298316 3:71413164 T ENSESTG00000023521 ENSESTT00000059363 Transcript intron_variant - - - - - - rs1298316 3:71413164 T 27086 NM_032682.5 Transcript intron_variant - - - - - - rs1298316 3:71413164 T 27086 NM_001244808.1 Transcript intron_variant - - - - - - rs1298316 3:71413164 T 27086 NM_001244816.1 Transcript intron_variant - - - - - - rs1298316 3:71413164 T 27086 NM_001244810.1 Transcript intron_variant - - - - - - rs704296 3:71730001 A - ENSR00001480533 RegulatoryFeature regulatory_region_variant - - - - - - rs704296 3:71730001 A CCDS33786.1 CCDS33786.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3832 rs704296 3:71730001 A 317649 NM_173359.4 Transcript 3_prime_UTR_variant 4609 - - - - - rs704296 3:71730001 A 317649 NM_001134650.1 Transcript 3_prime_UTR_variant 4524 - - - - - rs704296 3:71730001 A ENSESTG00000012781 ENSESTT00000032103 Transcript downstream_gene_variant - - - - - - DISTANCE=3692 rs704296 3:71730001 A CCDS46867.1 CCDS46867.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3832 rs704296 3:71730001 A 317649 NM_001134649.1 Transcript 3_prime_UTR_variant 4646 - - - - - rs704296 3:71730001 A 317649 NM_001134651.1 Transcript 3_prime_UTR_variant 4515 - - - - - rs704296 3:71730001 A ENSESTG00000012781 ENSESTT00000032095 Transcript downstream_gene_variant - - - - - - DISTANCE=3770 rs4677095 3:72174260 C ENSESTG00000012773 ENSESTT00000032054 Transcript intron_variant - - - - - - rs1438315 3:72455143 G 23429 NM_012234.5 Transcript intron_variant - - - - - - rs1438315 3:72455143 G ENSESTG00000012769 ENSESTT00000032044 Transcript intron_variant - - - - - - rs1976842 3:72484274 G 23429 NM_012234.5 Transcript intron_variant - - - - - - rs1976842 3:72484274 G ENSESTG00000012769 ENSESTT00000032044 Transcript intron_variant - - - - - - rs62249897 3:72950608 C 727936 NM_001080393.1 Transcript intron_variant - - - - - - rs62249897 3:72950608 C ENSESTG00000031716 ENSESTT00000080094 Transcript intron_variant - - - - - - rs62249897 3:72950608 C ENSESTG00000031716 ENSESTT00000080066 Transcript intron_variant - - - - - - rs62249897 3:72950608 C CCDS46870.1 CCDS46870.1 Transcript intron_variant - - - - - - rs6773599 3:73100625 G ENSESTG00000031716 ENSESTT00000080214 Transcript intron_variant - - - - - - rs6773599 3:73100625 G CCDS2917.1 CCDS2917.1 Transcript intron_variant - - - - - - rs6773599 3:73100625 G 151987 NM_174907.2 Transcript intron_variant - - - - - - rs6773599 3:73100625 G ENSESTG00000031716 ENSESTT00000080235 Transcript intron_variant - - - - - - rs6773599 3:73100625 G ENSESTG00000031716 ENSESTT00000080229 Transcript intron_variant - - - - - - rs6773599 3:73100625 G ENSESTG00000031716 ENSESTT00000080196 Transcript intron_variant - - - - - - rs6773599 3:73100625 G ENSESTG00000031716 ENSESTT00000080245 Transcript intron_variant - - - - - - rs9846903 3:73261965 G - - - intergenic_variant - - - - - - rs471670 3:73306669 C - - - intergenic_variant - - - - - - rs674891 3:73311652 A - - - intergenic_variant - - - - - - rs4677251 3:73358560 T - - - intergenic_variant - - - - - - rs1384174 3:73378862 G - - - intergenic_variant - - - - - - rs6798036 3:74417633 G 5067 NM_020872.1 Transcript intron_variant - - - - - - rs6798036 3:74417633 G ENSESTG00000021540 ENSESTT00000054044 Transcript downstream_gene_variant - - - - - - DISTANCE=1485 rs6798036 3:74417633 G CCDS33790.1 CCDS33790.1 Transcript intron_variant - - - - - - rs1488810 3:74426372 G 5067 NM_020872.1 Transcript intron_variant - - - - - - rs1488810 3:74426372 G ENSESTG00000021540 ENSESTT00000054044 Transcript intron_variant - - - - - - rs1488810 3:74426372 G CCDS33790.1 CCDS33790.1 Transcript intron_variant - - - - - - rs1488809 3:74426556 G 5067 NM_020872.1 Transcript intron_variant - - - - - - rs1488809 3:74426556 G ENSESTG00000021540 ENSESTT00000054044 Transcript intron_variant - - - - - - rs1488809 3:74426556 G CCDS33790.1 CCDS33790.1 Transcript intron_variant - - - - - - rs2200741 3:74431319 A 5067 NM_020872.1 Transcript intron_variant - - - - - - rs2200741 3:74431319 A ENSESTG00000021540 ENSESTT00000054044 Transcript intron_variant - - - - - - rs2200741 3:74431319 A CCDS33790.1 CCDS33790.1 Transcript intron_variant - - - - - - rs2200742 3:74434728 A 5067 NM_020872.1 Transcript intron_variant - - - - - - rs2200742 3:74434728 A ENSESTG00000021540 ENSESTT00000054044 Transcript intron_variant - - - - - - rs2200742 3:74434728 A CCDS33790.1 CCDS33790.1 Transcript intron_variant - - - - - - rs4677387 3:74435799 T 5067 NM_020872.1 Transcript intron_variant - - - - - - rs4677387 3:74435799 T ENSESTG00000021540 ENSESTT00000054044 Transcript intron_variant - - - - - - rs4677387 3:74435799 T CCDS33790.1 CCDS33790.1 Transcript intron_variant - - - - - - rs9859346 3:74539502 C 5067 NM_020872.1 Transcript intron_variant - - - - - - rs9859346 3:74539502 C ENSESTG00000021540 ENSESTT00000054044 Transcript intron_variant - - - - - - rs9859346 3:74539502 C CCDS33790.1 CCDS33790.1 Transcript intron_variant - - - - - - rs7653799 3:74541759 A 5067 NM_020872.1 Transcript intron_variant - - - - - - rs7653799 3:74541759 A ENSESTG00000021540 ENSESTT00000054044 Transcript intron_variant - - - - - - rs7653799 3:74541759 A CCDS33790.1 CCDS33790.1 Transcript intron_variant - - - - - - rs2323650 3:74885607 T - - - intergenic_variant - - - - - - rs6797851 3:74973727 T - - - intergenic_variant - - - - - - rs4677431 3:74977808 T - - - intergenic_variant - - - - - - rs4677509 3:75402978 G - - - intergenic_variant - - - - - - rs6549821 3:75965809 A 6092 NM_001128929.2 Transcript intron_variant - - - - - - rs4856028 3:75976655 A 6092 NM_001128929.2 Transcript intron_variant - - - - - - rs2324616 3:76506884 A 6092 NM_001128929.2 Transcript intron_variant - - - - - - rs2324616 3:76506884 A CCDS54609.1 CCDS54609.1 Transcript intron_variant - - - - - - rs264538 3:76749064 C 6092 NM_001128929.2 Transcript intron_variant - - - - - - rs264538 3:76749064 C CCDS54609.1 CCDS54609.1 Transcript intron_variant - - - - - - rs9860569 3:76884050 C - ENSR00001367782 RegulatoryFeature regulatory_region_variant - - - - - - rs9860569 3:76884050 C 6092 NM_001128929.2 Transcript intron_variant - - - - - - rs9860569 3:76884050 C CCDS54609.1 CCDS54609.1 Transcript intron_variant - - - - - - rs6762270 3:77060596 C 6092 NM_001128929.2 Transcript intron_variant - - - - - - rs6762270 3:77060596 C CCDS54609.1 CCDS54609.1 Transcript intron_variant - - - - - - rs7609921 3:77090805 C 6092 NM_001128929.2 Transcript intron_variant - - - - - - rs7609921 3:77090805 C 6092 NM_002942.4 Transcript intron_variant - - - - - - rs7609921 3:77090805 C CCDS43109.1 CCDS43109.1 Transcript intron_variant - - - - - - rs7609921 3:77090805 C CCDS54609.1 CCDS54609.1 Transcript intron_variant - - - - - - rs7609921 3:77090805 C ENSESTG00000000001 ENSESTT00000000001 Transcript intron_variant - - - - - - rs7630204 3:77143038 C 6092 NM_001128929.2 Transcript intron_variant - - - - - - rs7630204 3:77143038 C 6092 NM_002942.4 Transcript intron_variant - - - - - - rs7630204 3:77143038 C CCDS43109.1 CCDS43109.1 Transcript intron_variant - - - - - - rs7630204 3:77143038 C CCDS54609.1 CCDS54609.1 Transcript intron_variant - - - - - - rs7630204 3:77143038 C ENSESTG00000000001 ENSESTT00000000001 Transcript intron_variant - - - - - - rs775729 3:77639004 A ENSESTG00000032583 ENSESTT00000082303 Transcript intron_variant - - - - - - rs775729 3:77639004 A ENSESTG00000032583 ENSESTT00000082289 Transcript intron_variant - - - - - - rs775729 3:77639004 A ENSESTG00000032583 ENSESTT00000082297 Transcript intron_variant - - - - - - rs775729 3:77639004 A 6092 NM_002942.4 Transcript intron_variant - - - - - - rs775729 3:77639004 A CCDS43109.1 CCDS43109.1 Transcript intron_variant - - - - - - rs775729 3:77639004 A CCDS54609.1 CCDS54609.1 Transcript intron_variant - - - - - - rs775729 3:77639004 A ENSESTG00000032583 ENSESTT00000082306 Transcript intron_variant - - - - - - rs775729 3:77639004 A ENSESTG00000000002 ENSESTT00000000002 Transcript intron_variant - - - - - - rs775729 3:77639004 A 6092 NM_001128929.2 Transcript intron_variant - - - - - - rs776109 3:77743862 G - - - intergenic_variant - - - - - - rs9878050 3:77953842 C - - - intergenic_variant - - - - - - rs9822663 3:78212803 A - - - intergenic_variant - - - - - - rs5028902 3:78215938 A - - - intergenic_variant - - - - - - rs9824520 3:78230838 C - - - intergenic_variant - - - - - - rs6799740 3:78326685 C - - - intergenic_variant - - - - - - rs4283538 3:78488023 T - - - intergenic_variant - - - - - - rs1395783 3:78640189 T - - - intergenic_variant - - - - - - rs7634971 3:78711485 G ENSESTG00000024993 ENSESTT00000063099 Transcript upstream_gene_variant - - - - - - DISTANCE=1251 rs7634971 3:78711485 G CCDS46872.2 CCDS46872.2 Transcript intron_variant - - - - - - rs7634971 3:78711485 G CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs7634971 3:78711485 G 6091 NM_001145845.1 Transcript intron_variant - - - - - - rs7634971 3:78711485 G 6091 NM_133631.3 Transcript intron_variant - - - - - - rs7634971 3:78711485 G 6091 NM_002941.3 Transcript intron_variant - - - - - - rs7634971 3:78711485 G CCDS54610.1 CCDS54610.1 Transcript intron_variant - - - - - - rs7634971 3:78711485 G ENSESTG00000024993 ENSESTT00000063117 Transcript upstream_gene_variant - - - - - - DISTANCE=2589 rs1848248 3:78715424 C 6091 NM_002941.3 Transcript intron_variant - - - - - - rs1848248 3:78715424 C CCDS46872.2 CCDS46872.2 Transcript intron_variant - - - - - - rs1848248 3:78715424 C CCDS54610.1 CCDS54610.1 Transcript intron_variant - - - - - - rs1848248 3:78715424 C ENSESTG00000024941 ENSESTT00000063036 Transcript downstream_gene_variant - - - - - - DISTANCE=1654 rs1848248 3:78715424 C CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs1848248 3:78715424 C 6091 NM_001145845.1 Transcript intron_variant - - - - - - rs1848248 3:78715424 C 6091 NM_133631.3 Transcript intron_variant - - - - - - rs12632538 3:78739819 A CCDS46872.2 CCDS46872.2 Transcript intron_variant - - - - - - rs12632538 3:78739819 A ENSESTG00000024941 ENSESTT00000063036 Transcript intron_variant - - - - - - rs12632538 3:78739819 A CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs12632538 3:78739819 A 6091 NM_001145845.1 Transcript intron_variant - - - - - - rs12632538 3:78739819 A 6091 NM_133631.3 Transcript intron_variant - - - - - - rs12632538 3:78739819 A 6091 NM_002941.3 Transcript intron_variant - - - - - - rs12632538 3:78739819 A CCDS54610.1 CCDS54610.1 Transcript intron_variant - - - - - - rs12632538 3:78739819 A ENSESTG00000024941 ENSESTT00000063049 Transcript downstream_gene_variant - - - - - - DISTANCE=2219 rs9812722 3:78742819 G CCDS46872.2 CCDS46872.2 Transcript intron_variant - - - - - - rs9812722 3:78742819 G ENSESTG00000024941 ENSESTT00000063036 Transcript intron_variant - - - - - - rs9812722 3:78742819 G CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs9812722 3:78742819 G 6091 NM_001145845.1 Transcript intron_variant - - - - - - rs9812722 3:78742819 G 6091 NM_133631.3 Transcript intron_variant - - - - - - rs9812722 3:78742819 G 6091 NM_002941.3 Transcript intron_variant - - - - - - rs9812722 3:78742819 G CCDS54610.1 CCDS54610.1 Transcript intron_variant - - - - - - rs9812722 3:78742819 G ENSESTG00000024941 ENSESTT00000063049 Transcript intron_variant - - - - - - rs2608019 3:78768362 C CCDS46872.2 CCDS46872.2 Transcript intron_variant - - - - - - rs2608019 3:78768362 C ENSESTG00000024941 ENSESTT00000063036 Transcript upstream_gene_variant - - - - - - DISTANCE=1860 rs2608019 3:78768362 C CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs2608019 3:78768362 C 6091 NM_001145845.1 Transcript intron_variant - - - - - - rs2608019 3:78768362 C 6091 NM_133631.3 Transcript intron_variant - - - - - - rs2608019 3:78768362 C 6091 NM_002941.3 Transcript intron_variant - - - - - - rs2608019 3:78768362 C CCDS54610.1 CCDS54610.1 Transcript intron_variant - - - - - - rs2608019 3:78768362 C ENSESTG00000024898 ENSESTT00000062919 Transcript intron_variant - - - - - - rs2608019 3:78768362 C ENSESTG00000024941 ENSESTT00000063049 Transcript upstream_gene_variant - - - - - - DISTANCE=4692 rs2608024 3:78771657 T 6091 NM_002941.3 Transcript intron_variant - - - - - - rs2608024 3:78771657 T CCDS46872.2 CCDS46872.2 Transcript intron_variant - - - - - - rs2608024 3:78771657 T CCDS54610.1 CCDS54610.1 Transcript intron_variant - - - - - - rs2608024 3:78771657 T ENSESTG00000024898 ENSESTT00000062919 Transcript intron_variant - - - - - - rs2608024 3:78771657 T CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs2608024 3:78771657 T 6091 NM_001145845.1 Transcript intron_variant - - - - - - rs2608024 3:78771657 T 6091 NM_133631.3 Transcript intron_variant - - - - - - rs1513259 3:78788255 A 6091 NM_002941.3 Transcript intron_variant - - - - - - rs1513259 3:78788255 A CCDS46872.2 CCDS46872.2 Transcript intron_variant - - - - - - rs1513259 3:78788255 A CCDS54610.1 CCDS54610.1 Transcript intron_variant - - - - - - rs1513259 3:78788255 A ENSESTG00000024898 ENSESTT00000062919 Transcript intron_variant - - - - - - rs1513259 3:78788255 A CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs1513259 3:78788255 A 6091 NM_001145845.1 Transcript intron_variant - - - - - - rs1513259 3:78788255 A 6091 NM_133631.3 Transcript intron_variant - - - - - - rs333475 3:78825838 T CCDS46872.2 CCDS46872.2 Transcript intron_variant - - - - - - rs333475 3:78825838 T CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs333475 3:78825838 T 6091 NM_001145845.1 Transcript intron_variant - - - - - - rs333475 3:78825838 T 6091 NM_133631.3 Transcript intron_variant - - - - - - rs333475 3:78825838 T 6091 NM_002941.3 Transcript intron_variant - - - - - - rs333475 3:78825838 T ENSESTG00000024898 ENSESTT00000062858 Transcript intron_variant - - - - - - rs333475 3:78825838 T CCDS54610.1 CCDS54610.1 Transcript intron_variant - - - - - - rs333475 3:78825838 T ENSESTG00000024898 ENSESTT00000062919 Transcript intron_variant - - - - - - rs2121803 3:79029276 C CCDS46872.2 CCDS46872.2 Transcript intron_variant - - - - - - rs2121803 3:79029276 C CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs2121803 3:79029276 C 6091 NM_001145845.1 Transcript intron_variant - - - - - - rs2121803 3:79029276 C 6091 NM_133631.3 Transcript intron_variant - - - - - - rs2121803 3:79029276 C 6091 NM_002941.3 Transcript intron_variant - - - - - - rs2121803 3:79029276 C ENSESTG00000024898 ENSESTT00000062858 Transcript intron_variant - - - - - - rs2121803 3:79029276 C CCDS54610.1 CCDS54610.1 Transcript intron_variant - - - - - - rs2121803 3:79029276 C ENSESTG00000024898 ENSESTT00000062919 Transcript intron_variant - - - - - - rs6548613 3:79123488 G 6091 NM_002941.3 Transcript intron_variant - - - - - - rs6548613 3:79123488 G ENSESTG00000024898 ENSESTT00000062858 Transcript intron_variant - - - - - - rs6548613 3:79123488 G CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs1160639 3:79199458 T 6091 NM_002941.3 Transcript intron_variant - - - - - - rs1160639 3:79199458 T CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs1037617 3:79232745 G 6091 NM_002941.3 Transcript intron_variant - - - - - - rs1037617 3:79232745 G CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs991787 3:79368714 C 6091 NM_002941.3 Transcript intron_variant - - - - - - rs991787 3:79368714 C CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs4234351 3:79461887 A 6091 NM_002941.3 Transcript intron_variant - - - - - - rs4234351 3:79461887 A CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs7429582 3:79506445 T 6091 NM_002941.3 Transcript intron_variant - - - - - - rs7429582 3:79506445 T ENSESTG00000024875 ENSESTT00000062802 Transcript downstream_gene_variant - - - - - - DISTANCE=3017 rs7429582 3:79506445 T CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs9882761 3:79614914 T 6091 NM_002941.3 Transcript intron_variant - - - - - - rs9882761 3:79614914 T ENSESTG00000024884 ENSESTT00000062830 Transcript intron_variant - - - - - - rs9882761 3:79614914 T CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs9284799 3:79625615 C 6091 NM_002941.3 Transcript intron_variant - - - - - - rs9284799 3:79625615 C ENSESTG00000024884 ENSESTT00000062830 Transcript intron_variant - - - - - - rs9284799 3:79625615 C CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs4293670 3:79630556 G 6091 NM_002941.3 Transcript intron_variant - - - - - - rs4293670 3:79630556 G ENSESTG00000024884 ENSESTT00000062830 Transcript intron_variant - - - - - - rs4293670 3:79630556 G CCDS54611.1 CCDS54611.1 Transcript intron_variant - - - - - - rs9871862 3:79761038 C 6091 NM_002941.3 Transcript intron_variant - - - - - - rs9871862 3:79761038 C ENSESTG00000009003 ENSESTT00000022591 Transcript intron_variant - - - - - - rs6794403 3:79988939 C - - - intergenic_variant - - - - - - rs1822700 3:80200916 C - - - intergenic_variant - - - - - - rs2175077 3:80293935 T - - - intergenic_variant - - - - - - rs4241428 3:80599139 C - - - intergenic_variant - - - - - - rs491597 3:80677187 C - - - intergenic_variant - - - - - - rs676690 3:80754768 G - - - intergenic_variant - - - - - - rs2372450 3:80855097 C - - - intergenic_variant - - - - - - rs275361 3:81428028 A - - - intergenic_variant - - - - - - rs1389054 3:81636389 T 2632 NM_000158.3 Transcript intron_variant - - - - - - rs1389054 3:81636389 T CCDS54612.1 CCDS54612.1 Transcript intron_variant - - - - - - rs6762480 3:82225751 T - - - intergenic_variant - - - - - - rs6548833 3:82644354 A - - - intergenic_variant - - - - - - rs9858088 3:83250546 A - - - intergenic_variant - - - - - - rs2139205 3:83260747 T - - - intergenic_variant - - - - - - rs6771257 3:83284671 A - - - intergenic_variant - - - - - - rs7626876 3:83646543 A - - - intergenic_variant - - - - - - rs4619795 3:83967991 A - - - intergenic_variant - - - - - - rs9860374 3:84112030 G - - - intergenic_variant - - - - - - rs6548959 3:84476168 T - - - intergenic_variant - - - - - - rs1385657 3:84553005 G - - - intergenic_variant - - - - - - rs4370043 3:84566777 T - - - intergenic_variant - - - - - - rs1248852 3:84975830 C - - - intergenic_variant - - - - - - rs533529 3:85012980 A ENSESTG00000003385 ENSESTT00000008464 Transcript downstream_gene_variant - - - - - - DISTANCE=3392 rs533529 3:85012980 A CCDS54614.1 CCDS54614.1 Transcript intron_variant - - - - - - rs533529 3:85012980 A 253559 NM_001167674.1 Transcript intron_variant - - - - - - rs533529 3:85012980 A ENSESTG00000003385 ENSESTT00000008459 Transcript downstream_gene_variant - - - - - - DISTANCE=3392 rs533529 3:85012980 A 253559 NM_001167675.1 Transcript intron_variant - - - - - - rs533529 3:85012980 A CCDS54613.1 CCDS54613.1 Transcript intron_variant - - - - - - rs9844253 3:85248276 C CCDS54614.1 CCDS54614.1 Transcript intron_variant - - - - - - rs9844253 3:85248276 C 253559 NM_001167674.1 Transcript intron_variant - - - - - - rs9844253 3:85248276 C 253559 NM_001167675.1 Transcript intron_variant - - - - - - rs9844253 3:85248276 C CCDS54613.1 CCDS54613.1 Transcript intron_variant - - - - - - rs1597790 3:85262694 A CCDS54614.1 CCDS54614.1 Transcript intron_variant - - - - - - rs1597790 3:85262694 A 253559 NM_001167674.1 Transcript intron_variant - - - - - - rs1597790 3:85262694 A 253559 NM_001167675.1 Transcript intron_variant - - - - - - rs1597790 3:85262694 A CCDS54613.1 CCDS54613.1 Transcript intron_variant - - - - - - rs9839991 3:85338384 G CCDS54614.1 CCDS54614.1 Transcript intron_variant - - - - - - rs9839991 3:85338384 G 253559 NM_001167674.1 Transcript intron_variant - - - - - - rs9839991 3:85338384 G 253559 NM_001167675.1 Transcript intron_variant - - - - - - rs9839991 3:85338384 G CCDS54613.1 CCDS54613.1 Transcript intron_variant - - - - - - rs4298052 3:85727022 T 253559 NM_001256503.1 Transcript intron_variant - - - - - - rs4298052 3:85727022 T 253559 NM_001167674.1 Transcript intron_variant - - - - - - rs4298052 3:85727022 T 253559 NM_001256505.1 Transcript intron_variant - - - - - - rs4298052 3:85727022 T 253559 NM_001256504.1 Transcript intron_variant - - - - - - rs4298052 3:85727022 T CCDS54614.1 CCDS54614.1 Transcript intron_variant - - - - - - rs4298052 3:85727022 T 253559 NM_001256502.1 Transcript intron_variant - - - - - - rs4298052 3:85727022 T 253559 NM_001167675.1 Transcript intron_variant - - - - - - rs4298052 3:85727022 T CCDS54613.1 CCDS54613.1 Transcript intron_variant - - - - - - rs6794973 3:86192782 T - - - intergenic_variant - - - - - - rs9817569 3:86312922 T ENSESTG00000007672 ENSESTT00000019311 Transcript downstream_gene_variant - - - - - - DISTANCE=931 rs6792500 3:87308831 T CCDS2919.1 CCDS2919.1 Transcript downstream_gene_variant - - - - - - DISTANCE=213 rs6792500 3:87308831 T ENSESTG00000015967 ENSESTT00000040024 Transcript upstream_gene_variant - - - - - - DISTANCE=3564 rs6792500 3:87308831 T 5449 NM_000306.2 Transcript 3_prime_UTR_variant 1214 - - - - - rs6792500 3:87308831 T ENSESTG00000015964 ENSESTT00000040018 Transcript upstream_gene_variant - - - - - - DISTANCE=3004 rs6792500 3:87308831 T CCDS46873.1 CCDS46873.1 Transcript downstream_gene_variant - - - - - - DISTANCE=213 rs6792500 3:87308831 T 25978 NM_014043.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4133 rs6792500 3:87308831 T ENSESTG00000015906 ENSESTT00000039974 Transcript downstream_gene_variant - - - - - - DISTANCE=4857 rs6792500 3:87308831 T ENSESTG00000015956 ENSESTT00000040007 Transcript downstream_gene_variant - - - - - - DISTANCE=312 rs6792500 3:87308831 T ENSESTG00000015906 ENSESTT00000039980 Transcript downstream_gene_variant - - - - - - DISTANCE=4857 rs6792500 3:87308831 T 25978 NM_001244644.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4133 rs6792500 3:87308831 T 5449 NM_001122757.1 Transcript 3_prime_UTR_variant 1292 - - - - - rs7625687 3:88349777 T - - - intergenic_variant - - - - - - rs2344557 3:88366302 C - - - intergenic_variant - - - - - - rs6803192 3:88583008 A - - - intergenic_variant - - - - - - rs7650953 3:88584996 C - - - intergenic_variant - - - - - - rs1390705 3:89035328 C - - - intergenic_variant - - - - - - rs12053852 3:89043844 G - - - intergenic_variant - - - - - - rs9812211 3:89043971 T - - - intergenic_variant - - - - - - rs1496514 3:89065177 A - - - intergenic_variant - - - - - - rs2173040 3:89065957 A - - - intergenic_variant - - - - - - rs7427519 3:89280199 A CCDS2922.1 CCDS2922.1 Transcript intron_variant - - - - - - rs7427519 3:89280199 A 2042 NM_182644.2 Transcript intron_variant - - - - - - rs7427519 3:89280199 A CCDS46875.1 CCDS46875.1 Transcript intron_variant - - - - - - rs7427519 3:89280199 A 2042 NM_005233.5 Transcript intron_variant - - - - - - rs1093810 3:89681113 A - - - intergenic_variant - - - - - - rs6777254 3:89871673 T - - - intergenic_variant - - - - - - rs6768936 3:90144276 G - - - intergenic_variant - - - - - - rs9289236 3:93535787 A - - - intergenic_variant - - - - - - rs6808076 3:93978854 T - - - intergenic_variant - - - - - - rs493468 3:94066711 G - ENSR00001368726 RegulatoryFeature regulatory_region_variant - - - - - - rs493468 3:94066711 G - - - intergenic_variant - - - - - - rs534253 3:94129508 G - - - intergenic_variant - - - - - - rs566074 3:94129530 T - - - intergenic_variant - - - - - - rs6763443 3:94385810 G - - - intergenic_variant - - - - - - rs4143535 3:94442018 T - - - intergenic_variant - - - - - - rs9827258 3:94533284 A - - - intergenic_variant - - - - - - rs7628339 3:94572080 G - - - intergenic_variant - - - - - - rs4320060 3:94592151 A - - - intergenic_variant - - - - - - rs4857014 3:94606088 T - ENSR00001368761 RegulatoryFeature regulatory_region_variant - - - - - - rs4857014 3:94606088 T - - - intergenic_variant - - - - - - rs7630141 3:94608912 A - - - intergenic_variant - - - - - - rs7433860 3:94694459 C 255025 NR_015400.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3843867 3:94847871 A - - - intergenic_variant - - - - - - rs9860803 3:94951981 G - - - intergenic_variant - - - - - - rs1516615 3:94978691 G - - - intergenic_variant - - - - - - rs6437848 3:95150679 G - - - intergenic_variant - - - - - - rs4487239 3:95255741 A - - - intergenic_variant - - - - - - rs4626099 3:95264070 A - - - intergenic_variant - - - - - - rs1039957 3:95441611 C - - - intergenic_variant - - - - - - rs9818474 3:95504157 T - - - intergenic_variant - - - - - - rs7619467 3:95790757 G - - - intergenic_variant - - - - - - rs326304 3:96152668 A - - - intergenic_variant - - - - - - rs1487733 3:96318803 C - - - intergenic_variant - - - - - - rs10470429 3:96614552 C ENSESTG00000024999 ENSESTT00000063114 Transcript intron_variant - - - - - - rs10470429 3:96614552 C CCDS46876.1 CCDS46876.1 Transcript intron_variant - - - - - - rs10470429 3:96614552 C 285220 NM_001080448.2 Transcript intron_variant - - - - - - rs10934763 3:96755062 A CCDS46876.1 CCDS46876.1 Transcript intron_variant - - - - - - rs10934763 3:96755062 A 285220 NM_001080448.2 Transcript intron_variant - - - - - - rs2612286 3:96757058 A CCDS46876.1 CCDS46876.1 Transcript intron_variant - - - - - - rs2612286 3:96757058 A 285220 NM_001080448.2 Transcript intron_variant - - - - - - rs301964 3:97409105 C CCDS46876.1 CCDS46876.1 Transcript intron_variant - - - - - - rs301964 3:97409105 C 285220 NM_001080448.2 Transcript intron_variant - - - - - - rs1486455 3:97445827 T CCDS46876.1 CCDS46876.1 Transcript intron_variant - - - - - - rs1486455 3:97445827 T 285220 NM_001080448.2 Transcript intron_variant - - - - - - rs9861509 3:97450275 T ENSESTG00000025045 ENSESTT00000063216 Transcript upstream_gene_variant - - - - - - DISTANCE=4555 rs9861509 3:97450275 T CCDS46876.1 CCDS46876.1 Transcript intron_variant - - - - - - rs9861509 3:97450275 T 285220 NM_001080448.2 Transcript intron_variant - - - - - - rs832074 3:97698025 A - - - intergenic_variant - - - - - - rs1844936 3:97802837 C CCDS33796.1 CCDS33796.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3180 rs1844936 3:97802837 C 81050 NM_054106.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3180 rs828590 3:98455517 G ENSESTG00000029295 ENSESTT00000073858 Transcript intron_variant - - - - - - rs828590 3:98455517 G 100874207 NR_046683.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4022 rs828590 3:98455517 G ENSESTG00000029295 ENSESTT00000073849 Transcript intron_variant - - - - - - rs828590 3:98455517 G 10402 NM_006100.2 Transcript intron_variant - - - - - - rs828590 3:98455517 G ENSESTG00000029295 ENSESTT00000073820 Transcript intron_variant - - - - - - rs828612 3:98483968 T ENSESTG00000029295 ENSESTT00000073874 Transcript intron_variant - - - - - - rs828612 3:98483968 T ENSESTG00000029295 ENSESTT00000073858 Transcript intron_variant - - - - - - rs828612 3:98483968 T CCDS2933.1 CCDS2933.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3317 rs828612 3:98483968 T ENSESTG00000029295 ENSESTT00000073849 Transcript intron_variant - - - - - - rs828612 3:98483968 T 10402 NM_006100.2 Transcript intron_variant - - - - - - rs828612 3:98483968 T ENSESTG00000029295 ENSESTT00000073895 Transcript upstream_gene_variant - - - - - - DISTANCE=2739 rs828612 3:98483968 T ENSESTG00000029295 ENSESTT00000073820 Transcript intron_variant - - - - - - rs2119190 3:98602585 T CCDS46878.1 CCDS46878.1 Transcript intron_variant - - - - - - rs2119190 3:98602585 T ENSESTG00000029567 ENSESTT00000074608 Transcript intron_variant - - - - - - rs2119190 3:98602585 T ENSESTG00000029567 ENSESTT00000074561 Transcript intron_variant - - - - - - rs2119190 3:98602585 T 131566 NM_080927.3 Transcript intron_variant - - - - - - rs2119190 3:98602585 T ENSESTG00000029567 ENSESTT00000074637 Transcript intron_variant - - - - - - rs2119190 3:98602585 T ENSESTG00000029567 ENSESTT00000074633 Transcript intron_variant - - - - - - rs704593 3:98868711 A - - - intergenic_variant - - - - - - rs1398744 3:99241321 G ENSESTG00000029557 ENSESTT00000074350 Transcript intron_variant - - - - - - rs628813 3:99349891 G - - - intergenic_variant - - - - - - rs793451 3:99529789 A - - - intergenic_variant - - - - - - rs4244714 3:99679690 T 100500859 NR_037486.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3468 rs4244714 3:99679690 T ENSESTG00000009629 ENSESTT00000024135 Transcript intron_variant - - - - - - rs4244714 3:99679690 T 11259 NM_182909.2 Transcript intron_variant - - - - - - rs4244714 3:99679690 T ENSESTG00000009629 ENSESTT00000024131 Transcript intron_variant - - - - - - rs4244714 3:99679690 T 84319 NM_032359.3 Transcript intron_variant - - - - - - rs4244714 3:99679690 T CCDS2935.1 CCDS2935.1 Transcript intron_variant - - - - - - rs4244714 3:99679690 T 11259 NM_001042459.1 Transcript intron_variant - - - - - - rs6781325 3:99964886 A - ENSR00001369376 RegulatoryFeature regulatory_region_variant - - - - - - rs6781325 3:99964886 A - - - intergenic_variant - - - - - - rs2460718 3:100335488 C 84873 NM_032787.2 Transcript intron_variant - - - - - - rs2460718 3:100335488 C CCDS2938.1 CCDS2938.1 Transcript intron_variant - - - - - - rs2455873 3:100448337 A 10342 NM_001007565.2 Transcript intron_variant - - - - - - rs2455873 3:100448337 A 10342 NM_001195479.1 Transcript intron_variant - - - - - - rs2455873 3:100448337 A 10342 NM_006070.5 Transcript intron_variant - - - - - - rs2455873 3:100448337 A ENSESTG00000009518 ENSESTT00000023922 Transcript intron_variant - - - - - - rs2455873 3:100448337 A CCDS2939.1 CCDS2939.1 Transcript intron_variant - - - - - - rs2455873 3:100448337 A 10342 NM_001195478.1 Transcript intron_variant - - - - - - rs2455873 3:100448337 A ENSESTG00000009518 ENSESTT00000023898 Transcript intron_variant - - - - - - rs2455873 3:100448337 A ENSESTG00000009518 ENSESTT00000023916 Transcript intron_variant - - - - - - rs2455873 3:100448337 A CCDS56266.1 CCDS56266.1 Transcript intron_variant - - - - - - rs2460720 3:100450975 A 10342 NM_001007565.2 Transcript intron_variant - - - - - - rs2460720 3:100450975 A ENSESTG00000009518 ENSESTT00000023968 Transcript upstream_gene_variant - - - - - - DISTANCE=4443 rs2460720 3:100450975 A 10342 NM_001195479.1 Transcript intron_variant - - - - - - rs2460720 3:100450975 A 10342 NM_006070.5 Transcript intron_variant - - - - - - rs2460720 3:100450975 A ENSESTG00000009518 ENSESTT00000023922 Transcript intron_variant - - - - - - rs2460720 3:100450975 A CCDS2939.1 CCDS2939.1 Transcript intron_variant - - - - - - rs2460720 3:100450975 A 10342 NM_001195478.1 Transcript intron_variant - - - - - - rs2460720 3:100450975 A ENSESTG00000009518 ENSESTT00000023898 Transcript intron_variant - - - - - - rs2460720 3:100450975 A ENSESTG00000009518 ENSESTT00000023916 Transcript intron_variant - - - - - - rs2460720 3:100450975 A CCDS56266.1 CCDS56266.1 Transcript intron_variant - - - - - - rs1436940 3:100514390 C ENSESTG00000018142 ENSESTT00000045963 Transcript intron_variant - - - - - - rs1436940 3:100514390 C ENSESTG00000018142 ENSESTT00000045795 Transcript intron_variant - - - - - - rs1436940 3:100514390 C ENSESTG00000009567 ENSESTT00000024072 Transcript intron_variant - - - - - - rs1436940 3:100514390 C 25890 NM_015429.3 Transcript intron_variant - - - - - - rs1436940 3:100514390 C ENSESTG00000009567 ENSESTT00000024078 Transcript intron_variant - - - - - - rs1436940 3:100514390 C CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs1436940 3:100514390 C ENSESTG00000009567 ENSESTT00000024068 Transcript intron_variant - - - - - - rs1436940 3:100514390 C ENSESTG00000009567 ENSESTT00000024011 Transcript intron_variant - - - - - - rs2576373 3:100640954 A 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2576373 3:100640954 A ENSESTG00000017613 ENSESTT00000044326 Transcript upstream_gene_variant - - - - - - DISTANCE=3131 rs2576373 3:100640954 A ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2576373 3:100640954 A CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2576373 3:100640954 A ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2576374 3:100643353 C 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2576374 3:100643353 C ENSESTG00000017613 ENSESTT00000044326 Transcript upstream_gene_variant - - - - - - DISTANCE=732 rs2576374 3:100643353 C ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2576374 3:100643353 C CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2576374 3:100643353 C ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2576375 3:100644914 A 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2576375 3:100644914 A ENSESTG00000017613 ENSESTT00000044326 Transcript intron_variant - - - - - - rs2576375 3:100644914 A ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2576375 3:100644914 A CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2576375 3:100644914 A ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2576376 3:100645569 G 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2576376 3:100645569 G ENSESTG00000017613 ENSESTT00000044326 Transcript downstream_gene_variant - - - - - - DISTANCE=33 rs2576376 3:100645569 G ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2576376 3:100645569 G CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2576376 3:100645569 G ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2713745 3:100649115 T 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2713745 3:100649115 T ENSESTG00000017613 ENSESTT00000044326 Transcript downstream_gene_variant - - - - - - DISTANCE=3579 rs2713745 3:100649115 T ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2713745 3:100649115 T CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2713745 3:100649115 T ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs6799493 3:100653103 T 25890 NM_015429.3 Transcript intron_variant - - - - - - rs6799493 3:100653103 T ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs6799493 3:100653103 T CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs6799493 3:100653103 T ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2576383 3:100663414 T 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2576383 3:100663414 T ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2576383 3:100663414 T CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2576383 3:100663414 T ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2595891 3:100669851 C 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2595891 3:100669851 C ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2595891 3:100669851 C CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2595891 3:100669851 C ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2713744 3:100672310 A 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2713744 3:100672310 A ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2713744 3:100672310 A CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2713744 3:100672310 A ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2576392 3:100678743 T 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2576392 3:100678743 T ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2576392 3:100678743 T CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2576392 3:100678743 T ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2713785 3:100678989 T 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2713785 3:100678989 T ENSESTG00000017610 ENSESTT00000044316 Transcript intron_variant - - - - - - rs2713785 3:100678989 T CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2713785 3:100678989 T ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2595902 3:100695775 T 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2595902 3:100695775 T CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2595902 3:100695775 T ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2595901 3:100695789 A 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2595901 3:100695789 A CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2595901 3:100695789 A ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2576366 3:100696284 T 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2576366 3:100696284 T CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2576366 3:100696284 T ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2713760 3:100704347 T 25890 NM_015429.3 Transcript intron_variant - - - - - - rs2713760 3:100704347 T CCDS46880.1 CCDS46880.1 Transcript intron_variant - - - - - - rs2713760 3:100704347 T ENSESTG00000018012 ENSESTT00000045417 Transcript intron_variant - - - - - - rs2595905 3:100727246 C - - - intergenic_variant - - - - - - rs2713766 3:100743714 G - - - intergenic_variant - - - - - - rs2595915 3:100755339 C - ENSR00001369502 RegulatoryFeature regulatory_region_variant - - - - - - rs2595915 3:100755339 C - - - intergenic_variant - - - - - - rs2595887 3:100769285 C - ENSR00001481613 RegulatoryFeature regulatory_region_variant - - - - - - rs2595887 3:100769285 C - - - intergenic_variant - - - - - - rs2713740 3:100770792 A - - - intergenic_variant - - - - - - rs7427737 3:100780170 G - - - intergenic_variant - - - - - - rs7433703 3:100781919 G - - - intergenic_variant - - - - - - rs238836 3:100908170 T - ENSR00001369533 RegulatoryFeature regulatory_region_variant - - - - - - rs238836 3:100908170 T - - - intergenic_variant - - - - - - rs2660805 3:100923138 T - ENSR00001369538 RegulatoryFeature regulatory_region_variant - - - - - - rs2660805 3:100923138 T - - - intergenic_variant - - - - - - rs6441599 3:101081225 C CCDS43121.1 CCDS43121.1 Transcript intron_variant - - - - - - rs6441599 3:101081225 C CCDS2941.2 CCDS2941.2 Transcript intron_variant - - - - - - rs6441599 3:101081225 C 57337 NM_001077203.1 Transcript intron_variant - - - - - - rs6441599 3:101081225 C 57337 NM_020654.3 Transcript intron_variant - - - - - - rs6441599 3:101081225 C ENSESTG00000017874 ENSESTT00000045147 Transcript intron_variant - - - - - - rs6441603 3:101130380 C 100287852 XM_002342390.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2774 rs6441603 3:101130380 C ENSESTG00000017828 ENSESTT00000044996 Transcript intron_variant - - - - - - rs6441603 3:101130380 C CCDS2941.2 CCDS2941.2 Transcript intron_variant - - - - - - rs6441603 3:101130380 C 57337 NM_001077203.1 Transcript intron_variant - - - - - - rs6441603 3:101130380 C 57337 NM_020654.3 Transcript intron_variant - - - - - - rs6441603 3:101130380 C ENSESTG00000017828 ENSESTT00000044984 Transcript intron_variant - - - - - - rs6441603 3:101130380 C ENSESTG00000017828 ENSESTT00000044934 Transcript intron_variant - - - - - - rs6441603 3:101130380 C CCDS43121.1 CCDS43121.1 Transcript intron_variant - - - - - - rs6441603 3:101130380 C ENSESTG00000017828 ENSESTT00000044974 Transcript intron_variant - - - - - - rs6441603 3:101130380 C ENSESTG00000017828 ENSESTT00000044987 Transcript intron_variant - - - - - - rs2015127 3:101254597 G - - - intergenic_variant - - - - - - rs6804893 3:101282902 G 54931 NM_017819.2 Transcript intron_variant - - - - - - rs6804893 3:101282902 G ENSESTG00000017615 ENSESTT00000044402 Transcript intron_variant - - - - - - rs6804893 3:101282902 G CCDS43122.1 CCDS43122.1 Transcript upstream_gene_variant - - - - - - DISTANCE=724 rs6804893 3:101282902 G ENSESTG00000017615 ENSESTT00000044390 Transcript intron_variant - - - - - - rs1967976 3:101311905 C ENSESTG00000017630 ENSESTT00000044479 Transcript downstream_gene_variant - - - - - - DISTANCE=41 rs1967976 3:101311905 C ENSESTG00000017630 ENSESTT00000044535 Transcript downstream_gene_variant - - - - - - DISTANCE=41 rs1967976 3:101311905 C ENSESTG00000017630 ENSESTT00000044557 Transcript downstream_gene_variant - - - - - - DISTANCE=41 rs1967976 3:101311905 C 57092 NM_020357.1 Transcript 3_prime_UTR_variant 863 - - - - - rs1967976 3:101311905 C ENSESTG00000017630 ENSESTT00000044508 Transcript downstream_gene_variant - - - - - - DISTANCE=41 rs1967976 3:101311905 C ENSESTG00000017630 ENSESTT00000044576 Transcript downstream_gene_variant - - - - - - DISTANCE=41 rs1967976 3:101311905 C ENSESTG00000017812 ENSESTT00000044899 Transcript intron_variant - - - - - - rs1967976 3:101311905 C CCDS2942.1 CCDS2942.1 Transcript downstream_gene_variant - - - - - - DISTANCE=308 rs9837549 3:101389864 C CCDS2943.1 CCDS2943.1 Transcript intron_variant - - - - - - rs9837549 3:101389864 C ENSESTG00000017797 ENSESTT00000044848 Transcript intron_variant - - - - - - rs9837549 3:101389864 C 27107 NM_014415.3 Transcript intron_variant - - - - - - rs1365318 3:101410553 G 6152 NM_000986.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4990 rs9683356 3:101413963 A - - - intergenic_variant - - - - - - rs2264347 3:101433985 C 285359 NR_002941.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1725 rs994573 3:101443461 C - ENSR00001369634 RegulatoryFeature regulatory_region_variant - - - - - - rs994573 3:101443461 C CCDS2944.1 CCDS2944.1 Transcript upstream_gene_variant - - - - - - DISTANCE=60 rs994573 3:101443461 C 79598 NM_024548.2 Transcript upstream_gene_variant - - - - - - DISTANCE=33 rs994573 3:101443461 C ENSESTG00000017702 ENSESTT00000044655 Transcript upstream_gene_variant - - - - - - DISTANCE=2853 rs994573 3:101443461 C ENSESTG00000017702 ENSESTT00000044637 Transcript upstream_gene_variant - - - - - - DISTANCE=34 rs771827 3:101694770 G 152225 NR_026934.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs771768 3:101747661 G - - - intergenic_variant - - - - - - rs9844867 3:101812875 A - - - intergenic_variant - - - - - - rs9968162 3:102186178 A CCDS2947.1 CCDS2947.1 Transcript intron_variant - - - - - - rs9968162 3:102186178 A ENSESTG00000005522 ENSESTT00000014058 Transcript intron_variant - - - - - - rs9968162 3:102186178 A 131368 NM_175056.1 Transcript intron_variant - - - - - - rs1296373 3:102216215 A - - - intergenic_variant - - - - - - rs938422 3:102322917 C - - - intergenic_variant - - - - - - rs1399765 3:102346138 G - - - intergenic_variant - - - - - - rs1506434 3:102381203 G ENSESTG00000005530 ENSESTT00000014072 Transcript downstream_gene_variant - - - - - - DISTANCE=804 rs6780943 3:102466130 T - - - intergenic_variant - - - - - - rs163936 3:102699138 T - ENSR00001481744 RegulatoryFeature regulatory_region_variant - - - - - - rs163936 3:102699138 T - - - intergenic_variant - - - - - - rs346884 3:102770173 C - - - intergenic_variant - - - - - - rs1492877 3:102980231 G ENSESTG00000032868 ENSESTT00000083047 Transcript intron_variant - - - - - - rs6778423 3:103180504 T - - - intergenic_variant - - - - - - rs1184822 3:103722565 G - - - intergenic_variant - - - - - - rs9859582 3:104022298 T - - - intergenic_variant - - - - - - rs2713699 3:104053977 A - - - intergenic_variant - - - - - - rs9856162 3:104282306 A ENSESTG00000011182 ENSESTT00000028035 Transcript intron_variant - - - - - - rs812921 3:104468421 C - - - intergenic_variant - - - - - - rs4144911 3:104518496 C - - - intergenic_variant - - - - - - rs1836864 3:104658908 T - - - intergenic_variant - - - - - - rs1698969 3:104877895 A - - - intergenic_variant - - - - - - rs1698962 3:104907460 A - - - intergenic_variant - - - - - - rs4894923 3:105102083 T ENSESTG00000005228 ENSESTT00000013277 Transcript intron_variant - - - - - - rs4894923 3:105102083 T ENSESTG00000005149 ENSESTT00000013125 Transcript intron_variant - - - - - - rs4894923 3:105102083 T CCDS33810.1 CCDS33810.1 Transcript intron_variant - - - - - - rs4894923 3:105102083 T ENSESTG00000005149 ENSESTT00000013126 Transcript intron_variant - - - - - - rs4894923 3:105102083 T ENSESTG00000005149 ENSESTT00000013131 Transcript intron_variant - - - - - - rs4894923 3:105102083 T CCDS58841.1 CCDS58841.1 Transcript intron_variant - - - - - - rs4894923 3:105102083 T 214 NM_001627.3 Transcript intron_variant - - - - - - rs4894923 3:105102083 T 214 NM_001243283.1 Transcript intron_variant - - - - - - rs4894923 3:105102083 T 214 NM_001243281.1 Transcript intron_variant - - - - - - rs4894923 3:105102083 T 214 NM_001243280.1 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013147 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013125 Transcript intron_variant - - - - - - rs1552354 3:105230676 T CCDS33810.1 CCDS33810.1 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013154 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013131 Transcript intron_variant - - - - - - rs1552354 3:105230676 T 214 NM_001627.3 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013149 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013143 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013157 Transcript intron_variant - - - - - - rs1552354 3:105230676 T 214 NM_001243281.1 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005228 ENSESTT00000013277 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013140 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013133 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013137 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013151 Transcript intron_variant - - - - - - rs1552354 3:105230676 T ENSESTG00000005149 ENSESTT00000013126 Transcript intron_variant - - - - - - rs1552354 3:105230676 T CCDS58841.1 CCDS58841.1 Transcript intron_variant - - - - - - rs1552354 3:105230676 T 214 NM_001243283.1 Transcript intron_variant - - - - - - rs1552354 3:105230676 T 214 NM_001243280.1 Transcript intron_variant - - - - - - rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013147 Transcript downstream_gene_variant - - - - - - DISTANCE=139 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013125 Transcript downstream_gene_variant - - - - - - DISTANCE=139 rs633432 3:105272151 C CCDS33810.1 CCDS33810.1 Transcript intron_variant - - - - - - rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013154 Transcript downstream_gene_variant - - - - - - DISTANCE=1123 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013177 Transcript downstream_gene_variant - - - - - - DISTANCE=139 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013131 Transcript downstream_gene_variant - - - - - - DISTANCE=1123 rs633432 3:105272151 C 214 NM_001627.3 Transcript intron_variant - - - - - - rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013169 Transcript downstream_gene_variant - - - - - - DISTANCE=139 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013149 Transcript downstream_gene_variant - - - - - - DISTANCE=750 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013143 Transcript downstream_gene_variant - - - - - - DISTANCE=139 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013157 Transcript downstream_gene_variant - - - - - - DISTANCE=1123 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013172 Transcript downstream_gene_variant - - - - - - DISTANCE=1123 rs633432 3:105272151 C 214 NM_001243281.1 Transcript downstream_gene_variant - - - - - - DISTANCE=136 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013140 Transcript downstream_gene_variant - - - - - - DISTANCE=1123 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013133 Transcript downstream_gene_variant - - - - - - DISTANCE=139 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013137 Transcript downstream_gene_variant - - - - - - DISTANCE=750 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013126 Transcript downstream_gene_variant - - - - - - DISTANCE=750 rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013151 Transcript downstream_gene_variant - - - - - - DISTANCE=750 rs633432 3:105272151 C CCDS58841.1 CCDS58841.1 Transcript intron_variant - - - - - - rs633432 3:105272151 C ENSESTG00000005149 ENSESTT00000013171 Transcript downstream_gene_variant - - - - - - DISTANCE=750 rs633432 3:105272151 C 214 NM_001243280.1 Transcript intron_variant - - - - - - rs6437610 3:105387386 G CCDS2948.1 CCDS2948.1 Transcript intron_variant - - - - - - rs6437610 3:105387386 G ENSESTG00000005217 ENSESTT00000013268 Transcript intron_variant - - - - - - rs6437610 3:105387386 G ENSESTG00000005217 ENSESTT00000013263 Transcript intron_variant - - - - - - rs6437610 3:105387386 G ENSESTG00000005217 ENSESTT00000013266 Transcript intron_variant - - - - - - rs6437610 3:105387386 G 868 NM_170662.3 Transcript intron_variant - - - - - - rs9862133 3:105450624 A - ENSR00001369998 RegulatoryFeature regulatory_region_variant - - - - - - rs9862133 3:105450624 A ENSESTG00000005194 ENSESTT00000013229 Transcript intron_variant - - - - - - rs9862133 3:105450624 A CCDS2948.1 CCDS2948.1 Transcript intron_variant - - - - - - rs9862133 3:105450624 A 868 NM_170662.3 Transcript intron_variant - - - - - - rs7634020 3:105516875 T ENSESTG00000029127 ENSESTT00000073381 Transcript intron_variant - - - - - - rs7634020 3:105516875 T ENSESTG00000005194 ENSESTT00000013191 Transcript intron_variant - - - - - - rs7634020 3:105516875 T ENSESTG00000029127 ENSESTT00000073366 Transcript intron_variant - - - - - - rs7634020 3:105516875 T CCDS2948.1 CCDS2948.1 Transcript intron_variant - - - - - - rs7634020 3:105516875 T ENSESTG00000005194 ENSESTT00000013229 Transcript intron_variant - - - - - - rs7634020 3:105516875 T ENSESTG00000005194 ENSESTT00000013230 Transcript intron_variant - - - - - - rs7634020 3:105516875 T 868 NM_170662.3 Transcript intron_variant - - - - - - rs7634020 3:105516875 T ENSESTG00000029127 ENSESTT00000073334 Transcript intron_variant - - - - - - rs9876086 3:105541207 T - ENSR00001481842 RegulatoryFeature regulatory_region_variant - - - - - - rs9876086 3:105541207 T ENSESTG00000029127 ENSESTT00000073381 Transcript intron_variant - - - - - - rs9876086 3:105541207 T ENSESTG00000005194 ENSESTT00000013191 Transcript intron_variant - - - - - - rs9876086 3:105541207 T ENSESTG00000029127 ENSESTT00000073366 Transcript intron_variant - - - - - - rs9876086 3:105541207 T CCDS2948.1 CCDS2948.1 Transcript intron_variant - - - - - - rs9876086 3:105541207 T ENSESTG00000005194 ENSESTT00000013229 Transcript intron_variant - - - - - - rs9876086 3:105541207 T ENSESTG00000005194 ENSESTT00000013230 Transcript intron_variant - - - - - - rs9876086 3:105541207 T 868 NM_170662.3 Transcript intron_variant - - - - - - rs9876086 3:105541207 T ENSESTG00000029127 ENSESTT00000073334 Transcript intron_variant - - - - - - rs11924926 3:105559381 C ENSESTG00000029127 ENSESTT00000073381 Transcript intron_variant - - - - - - rs11924926 3:105559381 C ENSESTG00000005194 ENSESTT00000013191 Transcript intron_variant - - - - - - rs11924926 3:105559381 C ENSESTG00000029127 ENSESTT00000073366 Transcript intron_variant - - - - - - rs11924926 3:105559381 C CCDS2948.1 CCDS2948.1 Transcript intron_variant - - - - - - rs11924926 3:105559381 C ENSESTG00000005194 ENSESTT00000013229 Transcript intron_variant - - - - - - rs11924926 3:105559381 C ENSESTG00000005194 ENSESTT00000013230 Transcript intron_variant - - - - - - rs11924926 3:105559381 C 868 NM_170662.3 Transcript intron_variant - - - - - - rs11924926 3:105559381 C ENSESTG00000029127 ENSESTT00000073334 Transcript intron_variant - - - - - - rs340072 3:105705996 C - - - intergenic_variant - - - - - - rs7647048 3:105836747 A - - - intergenic_variant - - - - - - rs6437669 3:106146376 G ENSESTG00000029120 ENSESTT00000073300 Transcript upstream_gene_variant - - - - - - DISTANCE=835 rs7627084 3:106159796 A - - - intergenic_variant - - - - - - rs13079944 3:106424556 A - - - intergenic_variant - - - - - - rs1520721 3:106542196 A ENSESTG00000016832 ENSESTT00000042270 Transcript intron_variant - - - - - - rs4431104 3:106743724 A - - - intergenic_variant - - - - - - rs1528306 3:106844191 T ENSESTG00000016796 ENSESTT00000042142 Transcript intron_variant - - - - - - rs1528306 3:106844191 T 100302640 NR_028303.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1528306 3:106844191 T ENSESTG00000016796 ENSESTT00000042157 Transcript intron_variant - - - - - - rs1528306 3:106844191 T ENSESTG00000016796 ENSESTT00000042140 Transcript intron_variant - - - - - - rs9839535 3:107458428 A ENSESTG00000016713 ENSESTT00000042095 Transcript intron_variant - - - - - - rs9839535 3:107458428 A ENSESTG00000016713 ENSESTT00000042100 Transcript intron_variant - - - - - - rs9839535 3:107458428 A 56987 NM_020235.5 Transcript intron_variant - - - - - - rs9839535 3:107458428 A ENSESTG00000016713 ENSESTT00000042029 Transcript intron_variant - - - - - - rs9839535 3:107458428 A ENSESTG00000016713 ENSESTT00000041970 Transcript intron_variant - - - - - - rs9839535 3:107458428 A ENSESTG00000016713 ENSESTT00000042089 Transcript intron_variant - - - - - - rs9839535 3:107458428 A 56987 NM_001142568.1 Transcript intron_variant - - - - - - rs9839535 3:107458428 A CCDS46881.1 CCDS46881.1 Transcript intron_variant - - - - - - rs9839535 3:107458428 A CCDS2950.1 CCDS2950.1 Transcript intron_variant - - - - - - rs709444 3:107727024 G ENSESTG00000012984 ENSESTT00000032564 Transcript intron_variant - - - - - - rs162072 3:107902533 C ENSESTG00000013118 ENSESTT00000032896 Transcript intron_variant - - - - - - rs162072 3:107902533 C 55081 NM_018010.3 Transcript intron_variant - - - - - - rs162072 3:107902533 C ENSESTG00000013118 ENSESTT00000032905 Transcript intron_variant - - - - - - rs162072 3:107902533 C ENSESTG00000013118 ENSESTT00000032908 Transcript intron_variant - - - - - - rs162072 3:107902533 C CCDS2951.1 CCDS2951.1 Transcript intron_variant - - - - - - rs6768609 3:108134015 C CCDS43127.1 CCDS43127.1 Transcript intron_variant - - - - - - rs6768609 3:108134015 C 22989 NM_014981.1 Transcript intron_variant - - - - - - rs6768609 3:108134015 C ENSESTG00000013106 ENSESTT00000032843 Transcript upstream_gene_variant - - - - - - DISTANCE=752 rs2603123 3:108281040 T 57650 NM_020890.2 Transcript intron_variant - - - - - - rs2603123 3:108281040 T CCDS33812.1 CCDS33812.1 Transcript intron_variant - - - - - - rs2603123 3:108281040 T ENSESTG00000013088 ENSESTT00000032821 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032693 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032694 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032670 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032666 Transcript intron_variant - - - - - - rs3100637 3:108371149 T CCDS2952.1 CCDS2952.1 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032662 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032654 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032673 Transcript intron_variant - - - - - - rs3100637 3:108371149 T 9666 NM_014648.3 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032696 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032686 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032665 Transcript intron_variant - - - - - - rs3100637 3:108371149 T ENSESTG00000013011 ENSESTT00000032679 Transcript intron_variant - - - - - - rs2715680 3:108561479 C ENSESTG00000024641 ENSESTT00000062325 Transcript intron_variant - - - - - - rs2715680 3:108561479 C CCDS33813.1 CCDS33813.1 Transcript intron_variant - - - - - - rs2715680 3:108561479 C 50852 NM_016388.2 Transcript intron_variant - - - - - - rs2715680 3:108561479 C ENSESTG00000024641 ENSESTT00000062349 Transcript downstream_gene_variant - - - - - - DISTANCE=3307 rs2715680 3:108561479 C ENSESTG00000024641 ENSESTT00000062336 Transcript intron_variant - - - - - - rs6784432 3:108628159 G 9626 NM_005459.3 Transcript intron_variant - - - - - - rs6784432 3:108628159 G ENSESTG00000024949 ENSESTT00000063058 Transcript intron_variant - - - - - - rs6784432 3:108628159 G ENSESTG00000024949 ENSESTT00000063001 Transcript intron_variant - - - - - - rs6784432 3:108628159 G CCDS2954.1 CCDS2954.1 Transcript intron_variant - - - - - - rs1356071 3:108855774 G ENSESTG00000024690 ENSESTT00000062410 Transcript intron_variant - - - - - - rs1356071 3:108855774 G 401081 NR_033977.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1356071 3:108855774 G ENSESTG00000024690 ENSESTT00000062386 Transcript intron_variant - - - - - - rs2625594 3:109053031 T CCDS33814.1 CCDS33814.1 Transcript intron_variant - - - - - - rs2625594 3:109053031 T ENSESTG00000024717 ENSESTT00000062614 Transcript intron_variant - - - - - - rs2625594 3:109053031 T ENSESTG00000024717 ENSESTT00000062620 Transcript upstream_gene_variant - - - - - - DISTANCE=189 rs2625594 3:109053031 T ENSESTG00000024717 ENSESTT00000062599 Transcript intron_variant - - - - - - rs2625594 3:109053031 T 55211 NM_018189.3 Transcript intron_variant - - - - - - rs769515 3:109162354 C 401082 NM_001145553.1 Transcript intron_variant - - - - - - rs1732195 3:109337411 G - - - intergenic_variant - - - - - - rs2675764 3:109585973 A - - - intergenic_variant - - - - - - rs2675767 3:109592542 T - - - intergenic_variant - - - - - - rs1398415 3:110210507 A - - - intergenic_variant - - - - - - rs141726098 3:110551165 C - - - intergenic_variant - - - - - - rs12486322 3:110615825 T ENSESTG00000018075 ENSESTT00000045643 Transcript upstream_gene_variant - - - - - - DISTANCE=3766 rs12486322 3:110615825 T ENSESTG00000018075 ENSESTT00000045633 Transcript intron_variant - - - - - - rs12486322 3:110615825 T ENSESTG00000018075 ENSESTT00000045529 Transcript intron_variant - - - - - - rs12486322 3:110615825 T ENSESTG00000018075 ENSESTT00000045514 Transcript intron_variant - - - - - - rs1382074 3:110763952 C 100506555 NR_045114.1 Transcript downstream_gene_variant - - - - - - DISTANCE=210 rs1382074 3:110763952 C ENSESTG00000018075 ENSESTT00000045586 Transcript downstream_gene_variant - - - - - - DISTANCE=215 rs1382074 3:110763952 C ENSESTG00000018075 ENSESTT00000045572 Transcript downstream_gene_variant - - - - - - DISTANCE=1795 rs1382074 3:110763952 C ENSESTG00000018075 ENSESTT00000045529 Transcript intron_variant - - - - - - rs1382074 3:110763952 C ENSESTG00000018075 ENSESTT00000045514 Transcript intron_variant - - - - - - rs1382074 3:110763952 C ENSESTG00000018075 ENSESTT00000045503 Transcript downstream_gene_variant - - - - - - DISTANCE=215 rs1844241 3:111008545 C - - - intergenic_variant - - - - - - rs1497998 3:111183278 A - - - intergenic_variant - - - - - - rs2175749 3:111288447 A CCDS2958.1 CCDS2958.1 Transcript intron_variant - - - - - - rs2175749 3:111288447 A ENSESTG00000017984 ENSESTT00000045332 Transcript intron_variant - - - - - - rs2175749 3:111288447 A 10225 NM_198196.2 Transcript intron_variant - - - - - - rs2175749 3:111288447 A CCDS2959.1 CCDS2959.1 Transcript intron_variant - - - - - - rs2175749 3:111288447 A ENSESTG00000017984 ENSESTT00000045345 Transcript intron_variant - - - - - - rs2175749 3:111288447 A 10225 NM_005816.4 Transcript intron_variant - - - - - - rs1513329 3:111399334 T ENSESTG00000018032 ENSESTT00000045405 Transcript intron_variant - - - - - - rs1513329 3:111399334 T CCDS2961.1 CCDS2961.1 Transcript intron_variant - - - - - - rs1513329 3:111399334 T ENSESTG00000018048 ENSESTT00000045418 Transcript upstream_gene_variant - - - - - - DISTANCE=3054 rs1513329 3:111399334 T 257068 NM_153268.3 Transcript intron_variant - - - - - - rs1513329 3:111399334 T CCDS54619.1 CCDS54619.1 Transcript intron_variant - - - - - - rs1513329 3:111399334 T 257068 NM_001185106.1 Transcript intron_variant - - - - - - rs6804006 3:111408188 G ENSESTG00000018032 ENSESTT00000045405 Transcript intron_variant - - - - - - rs6804006 3:111408188 G CCDS2961.1 CCDS2961.1 Transcript intron_variant - - - - - - rs6804006 3:111408188 G 257068 NM_153268.3 Transcript intron_variant - - - - - - rs6804006 3:111408188 G CCDS54619.1 CCDS54619.1 Transcript intron_variant - - - - - - rs6804006 3:111408188 G 257068 NM_001185106.1 Transcript intron_variant - - - - - - rs6784525 3:111418184 G ENSESTG00000018032 ENSESTT00000045405 Transcript intron_variant - - - - - - rs6784525 3:111418184 G CCDS2961.1 CCDS2961.1 Transcript intron_variant - - - - - - rs6784525 3:111418184 G 257068 NM_153268.3 Transcript intron_variant - - - - - - rs6784525 3:111418184 G CCDS54619.1 CCDS54619.1 Transcript intron_variant - - - - - - rs6784525 3:111418184 G 257068 NM_001185106.1 Transcript intron_variant - - - - - - rs7635185 3:111434221 T ENSESTG00000018032 ENSESTT00000045405 Transcript intron_variant - - - - - - rs7635185 3:111434221 T CCDS2961.1 CCDS2961.1 Transcript intron_variant - - - - - - rs7635185 3:111434221 T 257068 NM_153268.3 Transcript intron_variant - - - - - - rs7635185 3:111434221 T CCDS54619.1 CCDS54619.1 Transcript intron_variant - - - - - - rs7635185 3:111434221 T 257068 NM_001185106.1 Transcript intron_variant - - - - - - rs9878397 3:111546668 G CCDS2961.1 CCDS2961.1 Transcript intron_variant - - - - - - rs9878397 3:111546668 G 90102 NM_001134437.1 Transcript intron_variant - - - - - - rs9878397 3:111546668 G 257068 NM_153268.3 Transcript intron_variant - - - - - - rs9878397 3:111546668 G 257068 NM_001185106.1 Transcript intron_variant - - - - - - rs9878397 3:111546668 G ENSESTG00000032574 ENSESTT00000082238 Transcript intron_variant - - - - - - rs2943236 3:111615063 G - ENSR00001482261 RegulatoryFeature regulatory_region_variant - - - - - - rs2943236 3:111615063 G CCDS46886.1 CCDS46886.1 Transcript intron_variant - - - - - - rs2943236 3:111615063 G 90102 NM_145753.2 Transcript intron_variant - - - - - - rs2943236 3:111615063 G ENSESTG00000032631 ENSESTT00000082374 Transcript intron_variant - - - - - - rs2943236 3:111615063 G CCDS2962.1 CCDS2962.1 Transcript intron_variant - - - - - - rs2943236 3:111615063 G 90102 NM_001134439.1 Transcript intron_variant - - - - - - rs2943236 3:111615063 G 90102 NM_001134437.1 Transcript intron_variant - - - - - - rs2943236 3:111615063 G 90102 NM_001134438.1 Transcript intron_variant - - - - - - rs2943236 3:111615063 G CCDS46885.1 CCDS46885.1 Transcript intron_variant - - - - - - rs1282937 3:111618332 C CCDS46886.1 CCDS46886.1 Transcript intron_variant - - - - - - rs1282937 3:111618332 C 90102 NM_145753.2 Transcript intron_variant - - - - - - rs1282937 3:111618332 C ENSESTG00000032631 ENSESTT00000082374 Transcript intron_variant - - - - - - rs1282937 3:111618332 C CCDS2962.1 CCDS2962.1 Transcript intron_variant - - - - - - rs1282937 3:111618332 C 90102 NM_001134439.1 Transcript intron_variant - - - - - - rs1282937 3:111618332 C 90102 NM_001134437.1 Transcript intron_variant - - - - - - rs1282937 3:111618332 C 90102 NM_001134438.1 Transcript intron_variant - - - - - - rs1282937 3:111618332 C CCDS46885.1 CCDS46885.1 Transcript intron_variant - - - - - - rs1282941 3:111638199 G ENSESTG00000032637 ENSESTT00000082437 Transcript intron_variant - - - - - - rs1282941 3:111638199 G CCDS46886.1 CCDS46886.1 Transcript intron_variant - - - - - - rs1282941 3:111638199 G 90102 NM_145753.2 Transcript intron_variant - - - - - - rs1282941 3:111638199 G CCDS2962.1 CCDS2962.1 Transcript intron_variant - - - - - - rs1282941 3:111638199 G 90102 NM_001134439.1 Transcript intron_variant - - - - - - rs1282941 3:111638199 G 90102 NM_001134437.1 Transcript intron_variant - - - - - - rs1282941 3:111638199 G 90102 NM_001134438.1 Transcript intron_variant - - - - - - rs1282941 3:111638199 G CCDS46885.1 CCDS46885.1 Transcript intron_variant - - - - - - rs774859 3:111685328 C CCDS46886.1 CCDS46886.1 Transcript intron_variant - - - - - - rs774859 3:111685328 C 90102 NM_145753.2 Transcript intron_variant - - - - - - rs774859 3:111685328 C ENSESTG00000032637 ENSESTT00000082531 Transcript intron_variant - - - - - - rs774859 3:111685328 C CCDS2962.1 CCDS2962.1 Transcript intron_variant - - - - - - rs774859 3:111685328 C 90102 NM_001134439.1 Transcript intron_variant - - - - - - rs774859 3:111685328 C ENSESTG00000032637 ENSESTT00000082521 Transcript intron_variant - - - - - - rs774859 3:111685328 C 90102 NM_001134437.1 Transcript intron_variant - - - - - - rs774859 3:111685328 C 90102 NM_001134438.1 Transcript intron_variant - - - - - - rs774859 3:111685328 C CCDS46885.1 CCDS46885.1 Transcript intron_variant - - - - - - rs703270 3:111699064 A CCDS2963.1 CCDS2963.1 Transcript intron_variant - - - - - - rs703270 3:111699064 A 55347 NM_018394.2 Transcript intron_variant - - - - - - rs703270 3:111699064 A 90102 NM_145753.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3700 rs703270 3:111699064 A ENSESTG00000032898 ENSESTT00000083156 Transcript intron_variant - - - - - - rs703270 3:111699064 A 90102 NM_001134439.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3700 rs703270 3:111699064 A 90102 NM_001134437.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3700 rs703270 3:111699064 A ENSESTG00000032898 ENSESTT00000083173 Transcript intron_variant - - - - - - rs703270 3:111699064 A ENSESTG00000032898 ENSESTT00000083164 Transcript intron_variant - - - - - - rs703270 3:111699064 A 90102 NM_001134438.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3700 rs774748 3:111712547 C CCDS2963.1 CCDS2963.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1979 rs774748 3:111712547 C 55347 NM_018394.2 Transcript downstream_gene_variant - - - - - - DISTANCE=337 rs774748 3:111712547 C ENSESTG00000032984 ENSESTT00000083421 Transcript upstream_gene_variant - - - - - - DISTANCE=4996 rs774748 3:111712547 C ENSESTG00000032898 ENSESTT00000083164 Transcript downstream_gene_variant - - - - - - DISTANCE=2280 rs774748 3:111712547 C ENSESTG00000032898 ENSESTT00000083156 Transcript downstream_gene_variant - - - - - - DISTANCE=2160 rs774746 3:111713738 A CCDS2963.1 CCDS2963.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3170 rs774746 3:111713738 A 55347 NM_018394.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1528 rs774746 3:111713738 A CCDS33816.1 CCDS33816.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4532 rs774746 3:111713738 A ENSESTG00000032984 ENSESTT00000083421 Transcript upstream_gene_variant - - - - - - DISTANCE=3805 rs774746 3:111713738 A 29114 NM_001008273.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4269 rs774746 3:111713738 A ENSESTG00000032898 ENSESTT00000083156 Transcript downstream_gene_variant - - - - - - DISTANCE=3351 rs774746 3:111713738 A 29114 NM_001008272.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3848 rs774746 3:111713738 A ENSESTG00000032898 ENSESTT00000083164 Transcript downstream_gene_variant - - - - - - DISTANCE=3471 rs774746 3:111713738 A 29114 NM_013259.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3848 rs4682360 3:111865242 T CCDS33817.1 CCDS33817.1 Transcript intron_variant - - - - - - rs4682360 3:111865242 T 285335 NM_183061.1 Transcript intron_variant - - - - - - rs4682360 3:111865242 T ENSESTG00000033460 ENSESTT00000084529 Transcript intron_variant - - - - - - rs4682085 3:111891163 T CCDS33817.1 CCDS33817.1 Transcript intron_variant - - - - - - rs4682085 3:111891163 T 285335 NM_183061.1 Transcript intron_variant - - - - - - rs6783808 3:112511803 G - - - intergenic_variant - - - - - - rs9834949 3:112536355 C CCDS43131.1 CCDS43131.1 Transcript intron_variant - - - - - - rs9834949 3:112536355 C CCDS56267.1 CCDS56267.1 Transcript intron_variant - - - - - - rs9834949 3:112536355 C 344807 NM_001008784.2 Transcript intron_variant - - - - - - rs9834949 3:112536355 C 344807 NM_001199215.1 Transcript intron_variant - - - - - - rs6438115 3:112635023 C - - - intergenic_variant - - - - - - rs2613950 3:112755919 G ENSESTG00000013548 ENSESTT00000033896 Transcript intron_variant - - - - - - rs9850997 3:112870518 T - ENSR00001482379 RegulatoryFeature regulatory_region_variant - - - - - - rs9850997 3:112870518 T - - - intergenic_variant - - - - - - rs6438155 3:113206920 T ENSESTG00000013677 ENSESTT00000034233 Transcript intron_variant - - - - - - rs6438155 3:113206920 T 152185 NM_144718.3 Transcript intron_variant - - - - - - rs6438155 3:113206920 T CCDS2973.1 CCDS2973.1 Transcript intron_variant - - - - - - rs2252142 3:113318372 C 100616476 NR_039648.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4583 rs2252142 3:113318372 C ENSESTG00000013638 ENSESTT00000034144 Transcript upstream_gene_variant - - - - - - DISTANCE=2877 rs2252142 3:113318372 C ENSESTG00000013638 ENSESTT00000034128 Transcript intron_variant - - - - - - rs2252142 3:113318372 C 54847 NM_017699.2 Transcript intron_variant - - - - - - rs2252142 3:113318372 C ENSESTG00000013638 ENSESTT00000034126 Transcript intron_variant - - - - - - rs2252142 3:113318372 C CCDS2974.1 CCDS2974.1 Transcript intron_variant - - - - - - rs2252142 3:113318372 C ENSESTG00000013638 ENSESTT00000034133 Transcript upstream_gene_variant - - - - - - DISTANCE=1831 rs2252142 3:113318372 C ENSESTG00000013638 ENSESTT00000034151 Transcript upstream_gene_variant - - - - - - DISTANCE=3285 rs930818 3:113373930 G CCDS43133.1 CCDS43133.1 Transcript missense_variant 6599 6599 2200 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs930818 3:113373930 G 205717 NM_001009899.2 Transcript missense_variant 7010 6599 2200 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs2712329 3:113560744 A ENSESTG00000022174 ENSESTT00000055966 Transcript intron_variant - - - - - - rs2712329 3:113560744 A 54762 NM_017577.4 Transcript intron_variant - - - - - - rs2712329 3:113560744 A CCDS33826.1 CCDS33826.1 Transcript intron_variant - - - - - - rs2712363 3:113585048 G ENSESTG00000022174 ENSESTT00000055966 Transcript intron_variant - - - - - - rs2712363 3:113585048 G 54762 NM_017577.4 Transcript intron_variant - - - - - - rs2712363 3:113585048 G CCDS33826.1 CCDS33826.1 Transcript intron_variant - - - - - - rs2566986 3:113589273 G ENSESTG00000022174 ENSESTT00000055966 Transcript intron_variant - - - - - - rs2566986 3:113589273 G 54762 NM_017577.4 Transcript intron_variant - - - - - - rs2566986 3:113589273 G CCDS33826.1 CCDS33826.1 Transcript intron_variant - - - - - - rs12486696 3:113816958 C - - - intergenic_variant - - - - - - rs4682147 3:113818084 G - - - intergenic_variant - - - - - - rs1564962 3:113819813 G - - - intergenic_variant - - - - - - rs7647270 3:113820868 A - - - intergenic_variant - - - - - - rs2654764 3:113868384 T CCDS33829.1 CCDS33829.1 Transcript intron_variant - - - - - - rs2654764 3:113868384 T 1814 NM_000796.3 Transcript intron_variant - - - - - - rs2654764 3:113868384 T ENSESTG00000022690 ENSESTT00000057306 Transcript intron_variant - - - - - - rs2654764 3:113868384 T CCDS2978.1 CCDS2978.1 Transcript intron_variant - - - - - - rs2654764 3:113868384 T 1814 NM_033663.3 Transcript intron_variant - - - - - - rs188958 3:113885886 A CCDS33829.1 CCDS33829.1 Transcript intron_variant - - - - - - rs188958 3:113885886 A 1814 NM_000796.3 Transcript intron_variant - - - - - - rs188958 3:113885886 A ENSESTG00000022690 ENSESTT00000057306 Transcript intron_variant - - - - - - rs188958 3:113885886 A CCDS2978.1 CCDS2978.1 Transcript intron_variant - - - - - - rs188958 3:113885886 A 1814 NM_033663.3 Transcript intron_variant - - - - - - rs170482 3:113891669 A CCDS33829.1 CCDS33829.1 Transcript upstream_gene_variant - - - - - - DISTANCE=830 rs170482 3:113891669 A 1814 NM_000796.3 Transcript intron_variant - - - - - - rs170482 3:113891669 A ENSESTG00000022690 ENSESTT00000057306 Transcript upstream_gene_variant - - - - - - DISTANCE=823 rs170482 3:113891669 A CCDS2978.1 CCDS2978.1 Transcript upstream_gene_variant - - - - - - DISTANCE=830 rs170482 3:113891669 A 1814 NM_033663.3 Transcript intron_variant - - - - - - rs324027 3:113892855 A CCDS33829.1 CCDS33829.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2016 rs324027 3:113892855 A 1814 NM_000796.3 Transcript intron_variant - - - - - - rs324027 3:113892855 A ENSESTG00000022690 ENSESTT00000057306 Transcript upstream_gene_variant - - - - - - DISTANCE=2009 rs324027 3:113892855 A CCDS2978.1 CCDS2978.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2016 rs324027 3:113892855 A 1814 NM_033663.3 Transcript intron_variant - - - - - - rs2693057 3:114120656 T ENSESTG00000022575 ENSESTT00000057216 Transcript intron_variant - - - - - - rs2693057 3:114120656 T 26137 NM_001164345.1 Transcript intron_variant - - - - - - rs2693057 3:114120656 T 26137 NM_001164346.1 Transcript intron_variant - - - - - - rs2693057 3:114120656 T ENSESTG00000022575 ENSESTT00000057223 Transcript intron_variant - - - - - - rs2693057 3:114120656 T 26137 NM_001164344.1 Transcript intron_variant - - - - - - rs2693057 3:114120656 T 26137 NM_001164343.1 Transcript intron_variant - - - - - - rs2693057 3:114120656 T 26137 NM_001164347.1 Transcript intron_variant - - - - - - rs2693057 3:114120656 T ENSESTG00000022575 ENSESTT00000057187 Transcript intron_variant - - - - - - rs2693057 3:114120656 T ENSESTG00000022575 ENSESTT00000057108 Transcript intron_variant - - - - - - rs2693057 3:114120656 T ENSESTG00000022575 ENSESTT00000057179 Transcript intron_variant - - - - - - rs2693057 3:114120656 T ENSESTG00000022575 ENSESTT00000057134 Transcript intron_variant - - - - - - rs2693057 3:114120656 T 26137 NM_015642.4 Transcript intron_variant - - - - - - rs2693057 3:114120656 T ENSESTG00000022575 ENSESTT00000057073 Transcript intron_variant - - - - - - rs10934273 3:114158701 T ENSESTG00000022575 ENSESTT00000057201 Transcript intron_variant - - - - - - rs10934273 3:114158701 T ENSESTG00000022575 ENSESTT00000057216 Transcript intron_variant - - - - - - rs10934273 3:114158701 T 26137 NM_001164345.1 Transcript intron_variant - - - - - - rs10934273 3:114158701 T 26137 NM_001164346.1 Transcript intron_variant - - - - - - rs10934273 3:114158701 T ENSESTG00000022575 ENSESTT00000057223 Transcript intron_variant - - - - - - rs10934273 3:114158701 T 26137 NM_001164344.1 Transcript intron_variant - - - - - - rs10934273 3:114158701 T 26137 NM_001164343.1 Transcript intron_variant - - - - - - rs10934273 3:114158701 T 26137 NM_001164347.1 Transcript intron_variant - - - - - - rs10934273 3:114158701 T ENSESTG00000022575 ENSESTT00000057187 Transcript intron_variant - - - - - - rs10934273 3:114158701 T ENSESTG00000022575 ENSESTT00000057108 Transcript intron_variant - - - - - - rs10934273 3:114158701 T ENSESTG00000022575 ENSESTT00000057179 Transcript intron_variant - - - - - - rs10934273 3:114158701 T ENSESTG00000022575 ENSESTT00000057134 Transcript intron_variant - - - - - - rs10934273 3:114158701 T 26137 NM_015642.4 Transcript intron_variant - - - - - - rs10934273 3:114158701 T ENSESTG00000022575 ENSESTT00000057073 Transcript intron_variant - - - - - - rs2244062 3:114328265 A 26137 NM_001164345.1 Transcript intron_variant - - - - - - rs2244062 3:114328265 A 26137 NM_001164346.1 Transcript intron_variant - - - - - - rs2244062 3:114328265 A 26137 NM_001164344.1 Transcript intron_variant - - - - - - rs2244062 3:114328265 A 26137 NM_001164343.1 Transcript intron_variant - - - - - - rs2244062 3:114328265 A 26137 NM_001164347.1 Transcript intron_variant - - - - - - rs2244062 3:114328265 A ENSESTG00000022575 ENSESTT00000057187 Transcript intron_variant - - - - - - rs2244062 3:114328265 A ENSESTG00000022575 ENSESTT00000057108 Transcript intron_variant - - - - - - rs2244062 3:114328265 A ENSESTG00000022575 ENSESTT00000057179 Transcript intron_variant - - - - - - rs2244062 3:114328265 A ENSESTG00000022575 ENSESTT00000057141 Transcript intron_variant - - - - - - rs2244062 3:114328265 A ENSESTG00000022575 ENSESTT00000057134 Transcript intron_variant - - - - - - rs2244062 3:114328265 A 26137 NM_015642.4 Transcript intron_variant - - - - - - rs2244062 3:114328265 A ENSESTG00000022575 ENSESTT00000057073 Transcript intron_variant - - - - - - rs2141770 3:114361120 T 26137 NM_001164345.1 Transcript intron_variant - - - - - - rs2141770 3:114361120 T 26137 NM_001164344.1 Transcript intron_variant - - - - - - rs2141770 3:114361120 T 26137 NM_001164343.1 Transcript intron_variant - - - - - - rs2141770 3:114361120 T ENSESTG00000022575 ENSESTT00000057108 Transcript intron_variant - - - - - - rs2141770 3:114361120 T ENSESTG00000022575 ENSESTT00000057134 Transcript intron_variant - - - - - - rs2141770 3:114361120 T ENSESTG00000022575 ENSESTT00000057141 Transcript intron_variant - - - - - - rs2141770 3:114361120 T 26137 NM_015642.4 Transcript intron_variant - - - - - - rs2141770 3:114361120 T ENSESTG00000022575 ENSESTT00000057073 Transcript intron_variant - - - - - - rs1274221 3:114451230 T 26137 NM_001164345.1 Transcript intron_variant - - - - - - rs1274221 3:114451230 T 26137 NM_001164344.1 Transcript intron_variant - - - - - - rs1274221 3:114451230 T ENSESTG00000035120 ENSESTT00000088738 Transcript intron_variant - - - - - - rs1274221 3:114451230 T 26137 NM_001164343.1 Transcript intron_variant - - - - - - rs1274221 3:114451230 T ENSESTG00000022575 ENSESTT00000057108 Transcript intron_variant - - - - - - rs1274221 3:114451230 T ENSESTG00000022575 ENSESTT00000057134 Transcript intron_variant - - - - - - rs1274221 3:114451230 T ENSESTG00000022575 ENSESTT00000057141 Transcript intron_variant - - - - - - rs1274221 3:114451230 T 26137 NM_015642.4 Transcript intron_variant - - - - - - rs1274221 3:114451230 T ENSESTG00000022575 ENSESTT00000057073 Transcript intron_variant - - - - - - rs7639234 3:114794001 T ENSESTG00000035120 ENSESTT00000088743 Transcript upstream_gene_variant - - - - - - DISTANCE=3779 rs7639234 3:114794001 T ENSESTG00000035120 ENSESTT00000088740 Transcript upstream_gene_variant - - - - - - DISTANCE=3736 rs7639234 3:114794001 T ENSESTG00000035120 ENSESTT00000088739 Transcript intron_variant - - - - - - rs7639234 3:114794001 T ENSESTG00000035120 ENSESTT00000088733 Transcript intron_variant - - - - - - rs7639234 3:114794001 T ENSESTG00000035120 ENSESTT00000088726 Transcript intron_variant - - - - - - rs7639234 3:114794001 T ENSESTG00000035120 ENSESTT00000088738 Transcript intron_variant - - - - - - rs7639234 3:114794001 T 26137 NM_001164343.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3740 rs7639234 3:114794001 T ENSESTG00000022575 ENSESTT00000057108 Transcript intron_variant - - - - - - rs7639234 3:114794001 T ENSESTG00000035120 ENSESTT00000088735 Transcript intron_variant - - - - - - rs7639234 3:114794001 T ENSESTG00000035120 ENSESTT00000088728 Transcript intron_variant - - - - - - rs7639234 3:114794001 T 26137 NM_015642.4 Transcript intron_variant - - - - - - rs7639234 3:114794001 T ENSESTG00000022575 ENSESTT00000057073 Transcript intron_variant - - - - - - rs6438233 3:114907278 A - - - intergenic_variant - - - - - - rs6786624 3:114992810 A - - - intergenic_variant - - - - - - rs1031677 3:115026225 T - - - intergenic_variant - - - - - - rs6809877 3:115239872 C ENSESTG00000035104 ENSESTT00000088698 Transcript intron_variant - - - - - - rs9833409 3:116077825 T ENSESTG00000028826 ENSESTT00000072526 Transcript intron_variant - - - - - - rs9833409 3:116077825 T CCDS2982.1 CCDS2982.1 Transcript intron_variant - - - - - - rs9833409 3:116077825 T 4045 NM_002338.3 Transcript intron_variant - - - - - - rs2867845 3:116449655 G - - - intergenic_variant - - - - - - rs891839 3:116496321 T - ENSR00001482608 RegulatoryFeature regulatory_region_variant - - - - - - rs891839 3:116496321 T - - - intergenic_variant - - - - - - rs7634249 3:116585870 A - - - intergenic_variant - - - - - - rs9289061 3:116612116 C - - - intergenic_variant - - - - - - rs12054312 3:117593944 T - - - intergenic_variant - - - - - - rs1447589 3:118007142 T - - - intergenic_variant - - - - - - rs779592 3:118029383 G - - - intergenic_variant - - - - - - rs696259 3:118460822 C - - - intergenic_variant - - - - - - rs4688001 3:119118104 G CCDS43135.1 CCDS43135.1 Transcript synonymous_variant 1065 1065 355 V gtA/gtG - rs4688001 3:119118104 G 57514 NM_020754.2 Transcript synonymous_variant 1597 1065 355 V gtA/gtG - rs4688001 3:119118104 G ENSESTG00000004169 ENSESTT00000010524 Transcript synonymous_variant 442 369 123 V gtA/gtG - rs4058490 3:119533910 C CCDS43136.1 CCDS43136.1 Transcript synonymous_variant 879 879 293 N aaT/aaC - rs4058490 3:119533910 C CCDS2995.1 CCDS2995.1 Transcript synonymous_variant 996 996 332 N aaT/aaC - rs4058490 3:119533910 C ENSESTG00000001737 ENSESTT00000004284 Transcript synonymous_variant 868 768 256 N aaT/aaC - rs4058490 3:119533910 C 8856 NM_033013.2 Transcript synonymous_variant 2607 768 256 N aaT/aaC - rs4058490 3:119533910 C CCDS54627.1 CCDS54627.1 Transcript synonymous_variant 768 768 256 N aaT/aaC - rs4058490 3:119533910 C ENSESTG00000001737 ENSESTT00000004292 Transcript synonymous_variant 1170 714 238 N aaT/aaC - rs4058490 3:119533910 C 8856 NM_003889.3 Transcript synonymous_variant 2718 879 293 N aaT/aaC - rs4058490 3:119533910 C 8856 NM_022002.2 Transcript synonymous_variant 1044 996 332 N aaT/aaC - rs2472683 3:119536926 G CCDS43136.1 CCDS43136.1 Transcript downstream_gene_variant - - - - - - DISTANCE=867 rs2472683 3:119536926 G CCDS2995.1 CCDS2995.1 Transcript downstream_gene_variant - - - - - - DISTANCE=867 rs2472683 3:119536926 G ENSESTG00000001737 ENSESTT00000004284 Transcript downstream_gene_variant - - - - - - DISTANCE=841 rs2472683 3:119536926 G 2932 NM_001146156.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3874 rs2472683 3:119536926 G 8856 NM_033013.2 Transcript 3_prime_UTR_variant 3900 - - - - - rs2472683 3:119536926 G CCDS54627.1 CCDS54627.1 Transcript downstream_gene_variant - - - - - - DISTANCE=867 rs2472683 3:119536926 G 2932 NM_002093.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3874 rs2472683 3:119536926 G ENSESTG00000001737 ENSESTT00000004292 Transcript downstream_gene_variant - - - - - - DISTANCE=841 rs2472683 3:119536926 G 8856 NM_003889.3 Transcript 3_prime_UTR_variant 4011 - - - - - rs2472683 3:119536926 G 8856 NM_022002.2 Transcript 3_prime_UTR_variant 2337 - - - - - rs6790162 3:119660149 G ENSESTG00000001824 ENSESTT00000004528 Transcript intron_variant - - - - - - rs6790162 3:119660149 G 2932 NM_002093.3 Transcript intron_variant - - - - - - rs6790162 3:119660149 G CCDS2996.1 CCDS2996.1 Transcript intron_variant - - - - - - rs6790162 3:119660149 G CCDS54628.1 CCDS54628.1 Transcript intron_variant - - - - - - rs6790162 3:119660149 G 2932 NM_001146156.1 Transcript intron_variant - - - - - - rs1492273 3:119964155 G CCDS54629.1 CCDS54629.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1210 rs1492273 3:119964155 G ENSESTG00000001818 ENSESTT00000004468 Transcript upstream_gene_variant - - - - - - DISTANCE=1011 rs1492273 3:119964155 G CCDS2997.1 CCDS2997.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1210 rs1492273 3:119964155 G 165829 NM_001168271.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1013 rs1492273 3:119964155 G 165829 NM_153002.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1013 rs386408 3:120523272 A - - - intergenic_variant - - - - - - rs668940 3:120674247 G CCDS43137.1 CCDS43137.1 Transcript intron_variant - - - - - - rs668940 3:120674247 G ENSESTG00000009475 ENSESTT00000023735 Transcript intron_variant - - - - - - rs668940 3:120674247 G 9515 NM_014980.2 Transcript intron_variant - - - - - - rs668940 3:120674247 G ENSESTG00000009475 ENSESTT00000023739 Transcript intron_variant - - - - - - rs668940 3:120674247 G ENSESTG00000009475 ENSESTT00000023744 Transcript intron_variant - - - - - - rs338972 3:120941543 T CCDS43137.1 CCDS43137.1 Transcript intron_variant - - - - - - rs338972 3:120941543 T ENSESTG00000009487 ENSESTT00000023763 Transcript intron_variant - - - - - - rs338972 3:120941543 T 9515 NM_014980.2 Transcript intron_variant - - - - - - rs4592967 3:121113196 A CCDS43137.1 CCDS43137.1 Transcript intron_variant - - - - - - rs4592967 3:121113196 A 9515 NM_014980.2 Transcript intron_variant - - - - - - rs532464 3:121210572 G CCDS33833.1 CCDS33833.1 Transcript intron_variant - - - - - - rs532464 3:121210572 G ENSESTG00000009560 ENSESTT00000023987 Transcript intron_variant - - - - - - rs532464 3:121210572 G 10721 NM_199420.3 Transcript intron_variant - - - - - - rs503025 3:121309752 C 51725 NM_016298.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2418 rs503025 3:121309752 C ENSESTG00000009506 ENSESTT00000023806 Transcript upstream_gene_variant - - - - - - DISTANCE=2424 rs503025 3:121309752 C CCDS33834.1 CCDS33834.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4305 rs503025 3:121309752 C 503582 NM_001012659.1 Transcript downstream_gene_variant - - - - - - DISTANCE=283 rs4676742 3:121463072 C 2804 NM_001256487.1 Transcript intron_variant - - - - - - rs4676742 3:121463072 C ENSESTG00000026163 ENSESTT00000066095 Transcript intron_variant - - - - - - rs4676742 3:121463072 C 2804 NM_001256488.1 Transcript intron_variant - - - - - - rs4676742 3:121463072 C 2804 NM_004487.4 Transcript intron_variant - - - - - - rs4676742 3:121463072 C 2804 NM_001256486.1 Transcript intron_variant - - - - - - rs6438716 3:121964047 G ENSESTG00000025518 ENSESTT00000064378 Transcript intron_variant - - - - - - rs6438716 3:121964047 G 846 NM_000388.3 Transcript intron_variant - - - - - - rs6438716 3:121964047 G ENSESTG00000026045 ENSESTT00000065624 Transcript intron_variant - - - - - - rs6438716 3:121964047 G 846 NM_001178065.1 Transcript intron_variant - - - - - - rs836863 3:122811042 G 10954 NM_006810.3 Transcript intron_variant - - - - - - rs836863 3:122811042 G 10954 NR_028444.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs836863 3:122811042 G CCDS3020.1 CCDS3020.1 Transcript intron_variant - - - - - - rs836863 3:122811042 G ENSESTG00000013778 ENSESTT00000034508 Transcript intron_variant - - - - - - rs836863 3:122811042 G ENSESTG00000013778 ENSESTT00000034518 Transcript intron_variant - - - - - - rs6783418 3:123518218 C 4638 NM_053028.3 Transcript intron_variant - - - - - - rs6783418 3:123518218 C 4638 NM_053025.3 Transcript intron_variant - - - - - - rs6783418 3:123518218 C ENSESTG00000010888 ENSESTT00000027271 Transcript intron_variant - - - - - - rs6783418 3:123518218 C ENSESTG00000010888 ENSESTT00000027268 Transcript intron_variant - - - - - - rs6783418 3:123518218 C 4638 NM_053026.3 Transcript intron_variant - - - - - - rs6783418 3:123518218 C 4638 NM_053027.3 Transcript intron_variant - - - - - - rs2682205 3:123556052 T 4638 NM_053028.3 Transcript intron_variant - - - - - - rs2682205 3:123556052 T 4638 NM_053025.3 Transcript intron_variant - - - - - - rs2682205 3:123556052 T ENSESTG00000010888 ENSESTT00000027268 Transcript intron_variant - - - - - - rs2682205 3:123556052 T 4638 NM_053026.3 Transcript intron_variant - - - - - - rs2682205 3:123556052 T 4638 NM_053027.3 Transcript intron_variant - - - - - - rs9844179 3:123949795 A ENSESTG00000010769 ENSESTT00000026950 Transcript intron_variant - - - - - - rs9844179 3:123949795 A 8997 NM_001024660.3 Transcript intron_variant - - - - - - rs9844179 3:123949795 A CCDS3027.1 CCDS3027.1 Transcript intron_variant - - - - - - rs9844179 3:123949795 A ENSESTG00000010769 ENSESTT00000026940 Transcript intron_variant - - - - - - rs9844179 3:123949795 A 8997 NM_003947.4 Transcript intron_variant - - - - - - rs9844179 3:123949795 A ENSESTG00000010769 ENSESTT00000026963 Transcript intron_variant - - - - - - rs4678109 3:124034590 T 8997 NM_001024660.3 Transcript intron_variant - - - - - - rs4678109 3:124034590 T ENSESTG00000010769 ENSESTT00000026971 Transcript intron_variant - - - - - - rs4678109 3:124034590 T CCDS3027.1 CCDS3027.1 Transcript intron_variant - - - - - - rs4678109 3:124034590 T ENSESTG00000010769 ENSESTT00000026972 Transcript intron_variant - - - - - - rs4678109 3:124034590 T 8997 NM_003947.4 Transcript intron_variant - - - - - - rs576069 3:124084379 C 8997 NM_001024660.3 Transcript intron_variant - - - - - - rs576069 3:124084379 C CCDS3027.1 CCDS3027.1 Transcript intron_variant - - - - - - rs576069 3:124084379 C 8997 NM_003947.4 Transcript intron_variant - - - - - - rs647010 3:124128938 G - ENSR00001372476 RegulatoryFeature regulatory_region_variant - - - - - - rs647010 3:124128938 G ENSESTG00000010784 ENSESTT00000027000 Transcript intron_variant - - - - - - rs647010 3:124128938 G ENSESTG00000010784 ENSESTT00000027003 Transcript intron_variant - - - - - - rs647010 3:124128938 G 8997 NM_001024660.3 Transcript intron_variant - - - - - - rs647010 3:124128938 G CCDS3027.1 CCDS3027.1 Transcript intron_variant - - - - - - rs647010 3:124128938 G 8997 NM_003947.4 Transcript intron_variant - - - - - - rs1712466 3:124832725 C ENSESTG00000035482 ENSESTT00000089613 Transcript intron_variant - - - - - - rs1712466 3:124832725 C 84561 NM_024628.5 Transcript intron_variant - - - - - - rs1712466 3:124832725 C CCDS43143.1 CCDS43143.1 Transcript intron_variant - - - - - - rs1712466 3:124832725 C ENSESTG00000035482 ENSESTT00000089614 Transcript upstream_gene_variant - - - - - - DISTANCE=3275 rs1712466 3:124832725 C 84561 NM_001195483.1 Transcript intron_variant - - - - - - rs489699 3:124848548 G - ENSR00001372673 RegulatoryFeature regulatory_region_variant - - - - - - rs489699 3:124848548 G ENSESTG00000035482 ENSESTT00000089613 Transcript intron_variant - - - - - - rs489699 3:124848548 G 84561 NM_024628.5 Transcript intron_variant - - - - - - rs489699 3:124848548 G CCDS43143.1 CCDS43143.1 Transcript intron_variant - - - - - - rs489699 3:124848548 G 84561 NM_001195483.1 Transcript intron_variant - - - - - - rs644751 3:124928155 C 84561 NM_024628.5 Transcript intron_variant - - - - - - rs644751 3:124928155 C ENSESTG00000035481 ENSESTT00000089605 Transcript intron_variant - - - - - - rs644751 3:124928155 C CCDS43143.1 CCDS43143.1 Transcript intron_variant - - - - - - rs644751 3:124928155 C ENSESTG00000035481 ENSESTT00000089607 Transcript intron_variant - - - - - - rs644751 3:124928155 C 84561 NM_001195483.1 Transcript intron_variant - - - - - - rs2979341 3:125341292 A - - - intergenic_variant - - - - - - rs2922206 3:125347575 A - - - intergenic_variant - - - - - - rs4467400 3:126120070 G ENSESTG00000015744 ENSESTT00000039409 Transcript intron_variant - - - - - - rs4467400 3:126120070 G CCDS3037.1 CCDS3037.1 Transcript intron_variant - - - - - - rs4467400 3:126120070 G 348807 NM_182628.2 Transcript intron_variant - - - - - - rs4467400 3:126120070 G ENSESTG00000015744 ENSESTT00000039405 Transcript intron_variant - - - - - - rs1627637 3:126158929 C CCDS43145.1 CCDS43145.1 Transcript intron_variant - - - - - - rs1627637 3:126158929 C CCDS3037.1 CCDS3037.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3682 rs1627637 3:126158929 C ENSESTG00000015768 ENSESTT00000039496 Transcript downstream_gene_variant - - - - - - DISTANCE=3264 rs1627637 3:126158929 C ENSESTG00000015788 ENSESTT00000039548 Transcript intron_variant - - - - - - rs1627637 3:126158929 C 79364 NM_025112.4 Transcript intron_variant - - - - - - rs1627637 3:126158929 C 348807 NM_182628.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3531 rs7612152 3:126276249 C CCDS3040.1 CCDS3040.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4016 rs7612152 3:126276249 C 152065 NM_152533.1 Transcript intron_variant - - - - - - rs4679263 3:126278302 A 152065 NM_152533.1 Transcript upstream_gene_variant - - - - - - DISTANCE=544 rs13081737 3:126543471 T ENSESTG00000022717 ENSESTT00000057426 Transcript intron_variant - - - - - - rs13081737 3:126543471 T 84303 NM_032343.2 Transcript intron_variant - - - - - - rs13081737 3:126543471 T CCDS3041.1 CCDS3041.1 Transcript intron_variant - - - - - - rs7647005 3:126553220 A ENSESTG00000022717 ENSESTT00000057426 Transcript intron_variant - - - - - - rs7647005 3:126553220 A 84303 NM_032343.2 Transcript intron_variant - - - - - - rs7647005 3:126553220 A CCDS3041.1 CCDS3041.1 Transcript intron_variant - - - - - - rs2885351 3:126684898 C - - - intergenic_variant - - - - - - rs934351 3:126760413 C 5361 NM_032242.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4178 rs6773189 3:126834995 G - - - intergenic_variant - - - - - - rs2358541 3:127176112 C - ENSR00001373121 RegulatoryFeature regulatory_region_variant - - - - - - rs2358541 3:127176112 C - - - intergenic_variant - - - - - - rs7633427 3:127659476 G ENSESTG00000006386 ENSESTT00000016129 Transcript intron_variant - - - - - - rs7633427 3:127659476 G ENSESTG00000006386 ENSESTT00000016124 Transcript intron_variant - - - - - - rs7633427 3:127659476 G 166348 NM_207335.2 Transcript intron_variant - - - - - - rs7633427 3:127659476 G ENSESTG00000006386 ENSESTT00000016136 Transcript intron_variant - - - - - - rs7633427 3:127659476 G CCDS33848.2 CCDS33848.2 Transcript intron_variant - - - - - - rs7633427 3:127659476 G ENSESTG00000006386 ENSESTT00000016132 Transcript intron_variant - - - - - - rs7630605 3:128148363 C - - - intergenic_variant - - - - - - rs900383 3:128733204 C - ENSR00001483429 RegulatoryFeature regulatory_region_variant - - - - - - rs900383 3:128733204 C 79825 NM_024768.2 Transcript intron_variant - - - - - - rs900383 3:128733204 C ENSESTG00000021544 ENSESTT00000054036 Transcript intron_variant - - - - - - rs900383 3:128733204 C CCDS3054.2 CCDS3054.2 Transcript intron_variant - - - - - - rs6805886 3:129185661 A 55764 NM_052990.1 Transcript intron_variant - - - - - - rs6805886 3:129185661 A CCDS3062.1 CCDS3062.1 Transcript intron_variant - - - - - - rs6805886 3:129185661 A 55764 NM_018262.2 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055658 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055861 Transcript intron_variant - - - - - - rs6805886 3:129185661 A 55764 NM_052985.2 Transcript intron_variant - - - - - - rs6805886 3:129185661 A 55764 NM_052989.1 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055841 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055820 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055854 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055777 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055819 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055844 Transcript intron_variant - - - - - - rs6805886 3:129185661 A CCDS3060.1 CCDS3060.1 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055817 Transcript intron_variant - - - - - - rs6805886 3:129185661 A CCDS3059.1 CCDS3059.1 Transcript intron_variant - - - - - - rs6805886 3:129185661 A CCDS3061.1 CCDS3061.1 Transcript intron_variant - - - - - - rs6805886 3:129185661 A ENSESTG00000021971 ENSESTT00000055667 Transcript intron_variant - - - - - - rs2713627 3:129279597 T - ENSR00001373650 RegulatoryFeature regulatory_region_variant - - - - - - rs2713627 3:129279597 T 23129 NM_015103.2 Transcript intron_variant - - - - - - rs2713627 3:129279597 T ENSESTG00000022257 ENSESTT00000056124 Transcript downstream_gene_variant - - - - - - DISTANCE=4513 rs2713627 3:129279597 T CCDS33854.1 CCDS33854.1 Transcript intron_variant - - - - - - rs4353839 3:130167189 T 256076 NM_153264.5 Transcript intron_variant - - - - - - rs4353839 3:130167189 T ENSESTG00000005381 ENSESTT00000013655 Transcript intron_variant - - - - - - rs4353839 3:130167189 T 256076 NR_022012.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs819081 3:130175936 G 256076 NM_153264.5 Transcript intron_variant - - - - - - rs819081 3:130175936 G ENSESTG00000005381 ENSESTT00000013655 Transcript intron_variant - - - - - - rs819081 3:130175936 G 256076 NR_022012.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2063217 3:130243053 G ENSESTG00000005385 ENSESTT00000013664 Transcript upstream_gene_variant - - - - - - DISTANCE=3707 rs2171187 3:131279987 A ENSESTG00000026548 ENSESTT00000067021 Transcript intron_variant - - - - - - rs2171187 3:131279987 A 131034 NM_130808.1 Transcript intron_variant - - - - - - rs2171187 3:131279987 A CCDS3072.1 CCDS3072.1 Transcript intron_variant - - - - - - rs4854873 3:131738694 C ENSESTG00000009472 ENSESTT00000023753 Transcript intron_variant - - - - - - rs4854873 3:131738694 C ENSESTG00000009472 ENSESTT00000023724 Transcript intron_variant - - - - - - rs4854873 3:131738694 C ENSESTG00000009472 ENSESTT00000023759 Transcript upstream_gene_variant - - - - - - DISTANCE=2095 rs4854873 3:131738694 C ENSESTG00000009472 ENSESTT00000023740 Transcript intron_variant - - - - - - rs4854873 3:131738694 C 131034 NM_130808.1 Transcript intron_variant - - - - - - rs821572 3:132360883 T - ENSR00001374100 RegulatoryFeature regulatory_region_variant - - - - - - rs821572 3:132360883 T CCDS3074.1 CCDS3074.1 Transcript missense_variant 470 470 157 R/H cGt/cAt - PolyPhen=benign;SIFT=tolerated rs821572 3:132360883 T 100532724 NR_037804.1 Transcript non_coding_exon_variant,nc_transcript_variant 4311 - - - - - rs821572 3:132360883 T ENSESTG00000023722 ENSESTT00000059948 Transcript downstream_gene_variant - - - - - - DISTANCE=4 rs821572 3:132360883 T 84129 NM_032169.4 Transcript missense_variant 850 470 157 R/H cGt/cAt - PolyPhen=benign;SIFT=tolerated rs9826414 3:132362375 C - ENSR00001374102 RegulatoryFeature regulatory_region_variant - - - - - - rs9826414 3:132362375 C CCDS3074.1 CCDS3074.1 Transcript intron_variant - - - - - - rs9826414 3:132362375 C 100532724 NR_037804.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9826414 3:132362375 C ENSESTG00000023722 ENSESTT00000059948 Transcript intron_variant - - - - - - rs9826414 3:132362375 C 84129 NM_032169.4 Transcript intron_variant - - - - - - rs1812334 3:132410848 T 100532724 NR_037804.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1812334 3:132410848 T CCDS3078.1 CCDS3078.1 Transcript intron_variant - - - - - - rs1812334 3:132410848 T 27031 NM_153240.4 Transcript intron_variant - - - - - - rs1197300 3:133114893 T 66000 NM_023943.2 Transcript 3_prime_UTR_variant 2065 - - - - - rs1197300 3:133114893 T 66000 NM_001136469.1 Transcript 3_prime_UTR_variant 2061 - - - - - rs1197300 3:133114893 T ENSESTG00000023324 ENSESTT00000058910 Transcript 3_prime_UTR_variant 1108 - - - - - rs1197300 3:133114893 T ENSESTG00000023370 ENSESTT00000058947 Transcript upstream_gene_variant - - - - - - DISTANCE=4038 rs1197300 3:133114893 T 8419 NM_003571.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3897 rs1197300 3:133114893 T CCDS33858.1 CCDS33858.1 Transcript downstream_gene_variant - - - - - - DISTANCE=63 rs1197300 3:133114893 T ENSESTG00000023370 ENSESTT00000058926 Transcript upstream_gene_variant - - - - - - DISTANCE=4025 rs1197300 3:133114893 T CCDS33859.1 CCDS33859.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4035 rs1197300 3:133114893 T ENSESTG00000023370 ENSESTT00000058958 Transcript upstream_gene_variant - - - - - - DISTANCE=4413 rs6439407 3:133180337 T - ENSR00001374199 RegulatoryFeature regulatory_region_variant - - - - - - rs6439407 3:133180337 T ENSESTG00000023391 ENSESTT00000059053 Transcript intron_variant - - - - - - rs6439407 3:133180337 T CCDS33859.1 CCDS33859.1 Transcript intron_variant - - - - - - rs6439407 3:133180337 T 8419 NM_003571.2 Transcript intron_variant - - - - - - rs6439417 3:133226101 T - - - intergenic_variant - - - - - - rs6779085 3:133303600 G CCDS3079.1 CCDS3079.1 Transcript intron_variant - - - - - - rs6779085 3:133303600 G 55573 NM_017548.4 Transcript intron_variant - - - - - - rs6779085 3:133303600 G 55573 NM_001134423.1 Transcript intron_variant - - - - - - rs6779085 3:133303600 G CCDS46917.1 CCDS46917.1 Transcript intron_variant - - - - - - rs6779085 3:133303600 G ENSESTG00000023512 ENSESTT00000059376 Transcript intron_variant - - - - - - rs6779085 3:133303600 G CCDS46918.1 CCDS46918.1 Transcript intron_variant - - - - - - rs6779085 3:133303600 G 55573 NM_001134422.1 Transcript intron_variant - - - - - - rs6779085 3:133303600 G ENSESTG00000023512 ENSESTT00000059354 Transcript intron_variant - - - - - - rs7630626 3:133705134 A ENSESTG00000015425 ENSESTT00000038655 Transcript intron_variant - - - - - - rs7630626 3:133705134 A CCDS3084.1 CCDS3084.1 Transcript intron_variant - - - - - - rs7630626 3:133705134 A 6578 NM_005630.2 Transcript intron_variant - - - - - - rs7630626 3:133705134 A ENSESTG00000015425 ENSESTT00000038657 Transcript intron_variant - - - - - - rs7630626 3:133705134 A ENSESTG00000015425 ENSESTT00000038616 Transcript intron_variant - - - - - - rs7634394 3:133906692 T 6259 NM_002958.3 Transcript intron_variant - - - - - - rs7634394 3:133906692 T ENSESTG00000015328 ENSESTT00000038535 Transcript intron_variant - - - - - - rs7634394 3:133906692 T ENSESTG00000015328 ENSESTT00000038545 Transcript intron_variant - - - - - - rs7634394 3:133906692 T ENSESTG00000015328 ENSESTT00000038597 Transcript intron_variant - - - - - - rs7634394 3:133906692 T 6259 NM_001005861.2 Transcript intron_variant - - - - - - rs7634394 3:133906692 T ENSESTG00000015328 ENSESTT00000038561 Transcript intron_variant - - - - - - rs7634394 3:133906692 T ENSESTG00000015328 ENSESTT00000038601 Transcript upstream_gene_variant - - - - - - DISTANCE=4445 rs7634394 3:133906692 T ENSESTG00000015328 ENSESTT00000038551 Transcript intron_variant - - - - - - rs6778661 3:134395383 A ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs6778661 3:134395383 A ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs6439509 3:134405990 G ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs6439509 3:134405990 G ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs1466079 3:134414273 C - ENSR00001483873 RegulatoryFeature regulatory_region_variant - - - - - - rs1466079 3:134414273 C ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs1466079 3:134414273 C ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs4955446 3:134422278 T ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs4955446 3:134422278 T ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs6781714 3:134423925 C ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs6781714 3:134423925 C ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs4955474 3:134430042 G ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs4955474 3:134430042 G ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs1447682 3:134432410 C ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs1447682 3:134432410 C ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs10935126 3:134436559 T ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs10935126 3:134436559 T ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs4955482 3:134442840 G ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs4955482 3:134442840 G ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs1374816 3:134455945 T ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs1374816 3:134455945 T ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs7610204 3:134467689 G ENSESTG00000015243 ENSESTT00000038178 Transcript intron_variant - - - - - - rs7610204 3:134467689 G ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs7611084 3:134547183 C 2047 NM_004441.4 Transcript intron_variant - - - - - - rs7611084 3:134547183 C ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs7611084 3:134547183 C CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs7611084 3:134547183 C ENSESTG00000032579 ENSESTT00000082277 Transcript intron_variant - - - - - - rs7611084 3:134547183 C ENSESTG00000032579 ENSESTT00000082271 Transcript intron_variant - - - - - - rs6797902 3:134581593 A 2047 NM_004441.4 Transcript intron_variant - - - - - - rs6797902 3:134581593 A ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs6797902 3:134581593 A CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs6797902 3:134581593 A ENSESTG00000032579 ENSESTT00000082277 Transcript intron_variant - - - - - - rs6797902 3:134581593 A ENSESTG00000032579 ENSESTT00000082284 Transcript intron_variant - - - - - - rs6797902 3:134581593 A ENSESTG00000032579 ENSESTT00000082271 Transcript intron_variant - - - - - - rs12108179 3:134581994 C 2047 NM_004441.4 Transcript intron_variant - - - - - - rs12108179 3:134581994 C ENSESTG00000015243 ENSESTT00000038199 Transcript intron_variant - - - - - - rs12108179 3:134581994 C CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs12108179 3:134581994 C ENSESTG00000032579 ENSESTT00000082277 Transcript intron_variant - - - - - - rs12108179 3:134581994 C ENSESTG00000032579 ENSESTT00000082284 Transcript intron_variant - - - - - - rs12108179 3:134581994 C ENSESTG00000032579 ENSESTT00000082271 Transcript intron_variant - - - - - - rs6439550 3:134773238 A 2047 NM_004441.4 Transcript intron_variant - - - - - - rs6439550 3:134773238 A CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs9863262 3:134782505 A 2047 NM_004441.4 Transcript intron_variant - - - - - - rs9863262 3:134782505 A CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs6780733 3:134812465 G 2047 NM_004441.4 Transcript intron_variant - - - - - - rs6780733 3:134812465 G CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs6803119 3:134836973 T 2047 NM_004441.4 Transcript intron_variant - - - - - - rs6803119 3:134836973 T CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs2140767 3:134838942 A 2047 NM_004441.4 Transcript intron_variant - - - - - - rs2140767 3:134838942 A CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs1404580 3:134840849 A 2047 NM_004441.4 Transcript intron_variant - - - - - - rs1404580 3:134840849 A CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs1404578 3:134848863 A ENSESTG00000032599 ENSESTT00000082320 Transcript upstream_gene_variant - - - - - - DISTANCE=2717 rs1404578 3:134848863 A 2047 NM_004441.4 Transcript intron_variant - - - - - - rs1404578 3:134848863 A ENSESTG00000032599 ENSESTT00000082326 Transcript upstream_gene_variant - - - - - - DISTANCE=2771 rs1404578 3:134848863 A CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs6439558 3:134852587 T ENSESTG00000032599 ENSESTT00000082320 Transcript intron_variant - - - - - - rs6439558 3:134852587 T 2047 NM_004441.4 Transcript intron_variant - - - - - - rs6439558 3:134852587 T ENSESTG00000032599 ENSESTT00000082326 Transcript intron_variant - - - - - - rs6439558 3:134852587 T CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs1501197 3:134854914 A ENSESTG00000032599 ENSESTT00000082320 Transcript intron_variant - - - - - - rs1501197 3:134854914 A 2047 NM_004441.4 Transcript intron_variant - - - - - - rs1501197 3:134854914 A ENSESTG00000032599 ENSESTT00000082326 Transcript intron_variant - - - - - - rs1501197 3:134854914 A CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs1501196 3:134856407 A ENSESTG00000032599 ENSESTT00000082320 Transcript intron_variant - - - - - - rs1501196 3:134856407 A 2047 NM_004441.4 Transcript intron_variant - - - - - - rs1501196 3:134856407 A ENSESTG00000032599 ENSESTT00000082326 Transcript intron_variant - - - - - - rs1501196 3:134856407 A CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs9813044 3:134859516 G ENSESTG00000032599 ENSESTT00000082320 Transcript intron_variant - - - - - - rs9813044 3:134859516 G 2047 NM_004441.4 Transcript intron_variant - - - - - - rs9813044 3:134859516 G ENSESTG00000032599 ENSESTT00000082326 Transcript intron_variant - - - - - - rs9813044 3:134859516 G CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs6798510 3:134870803 T ENSESTG00000032599 ENSESTT00000082320 Transcript intron_variant - - - - - - rs6798510 3:134870803 T 2047 NM_004441.4 Transcript intron_variant - - - - - - rs6798510 3:134870803 T ENSESTG00000032599 ENSESTT00000082326 Transcript intron_variant - - - - - - rs6798510 3:134870803 T CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs924543 3:134878545 G ENSESTG00000032599 ENSESTT00000082320 Transcript intron_variant - - - - - - rs924543 3:134878545 G 2047 NM_004441.4 Transcript intron_variant - - - - - - rs924543 3:134878545 G CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs1501216 3:134947230 C 2047 NM_004441.4 Transcript intron_variant - - - - - - rs1501216 3:134947230 C CCDS46921.1 CCDS46921.1 Transcript intron_variant - - - - - - rs2400564 3:135261721 C - - - intergenic_variant - - - - - - rs6439580 3:135292763 T - - - intergenic_variant - - - - - - rs979902 3:135294171 T - - - intergenic_variant - - - - - - rs1910120 3:135297289 C - - - intergenic_variant - - - - - - rs12639401 3:135297933 A - - - intergenic_variant - - - - - - rs987451 3:135317079 C - - - intergenic_variant - - - - - - rs2400565 3:135317301 G - - - intergenic_variant - - - - - - rs6439584 3:135344726 C - - - intergenic_variant - - - - - - rs10755088 3:135352446 G - - - intergenic_variant - - - - - - rs2084352 3:135384009 C - - - intergenic_variant - - - - - - rs1447601 3:135405341 G - - - intergenic_variant - - - - - - rs6768937 3:135406147 G - - - intergenic_variant - - - - - - rs1982351 3:135414348 C - - - intergenic_variant - - - - - - rs1348970 3:135416580 T - - - intergenic_variant - - - - - - rs1374772 3:135416918 C - - - intergenic_variant - - - - - - rs9881565 3:135442147 A - - - intergenic_variant - - - - - - rs6784275 3:135451334 G - - - intergenic_variant - - - - - - rs1278494 3:135823337 G ENSESTG00000030943 ENSESTT00000078048 Transcript intron_variant - - - - - - rs1278494 3:135823337 G ENSESTG00000031341 ENSESTT00000079028 Transcript intron_variant - - - - - - rs1278494 3:135823337 G ENSESTG00000030943 ENSESTT00000077952 Transcript intron_variant - - - - - - rs1278494 3:135823337 G 5523 NM_001190447.1 Transcript intron_variant - - - - - - rs1278494 3:135823337 G ENSESTG00000030943 ENSESTT00000078030 Transcript intron_variant - - - - - - rs1278494 3:135823337 G CCDS3088.1 CCDS3088.1 Transcript intron_variant - - - - - - rs1278494 3:135823337 G CCDS54642.1 CCDS54642.1 Transcript intron_variant - - - - - - rs1278494 3:135823337 G 5523 NM_181897.2 Transcript intron_variant - - - - - - rs1278494 3:135823337 G 5523 NM_002718.4 Transcript intron_variant - - - - - - rs1278494 3:135823337 G CCDS3087.1 CCDS3087.1 Transcript intron_variant - - - - - - rs1983070 3:135868204 T ENSESTG00000031311 ENSESTT00000078992 Transcript downstream_gene_variant - - - - - - DISTANCE=3012 rs1983070 3:135868204 T ENSESTG00000030943 ENSESTT00000078048 Transcript downstream_gene_variant - - - - - - DISTANCE=3925 rs1983070 3:135868204 T ENSESTG00000031311 ENSESTT00000078976 Transcript downstream_gene_variant - - - - - - DISTANCE=2844 rs1983070 3:135868204 T ENSESTG00000031341 ENSESTT00000079028 Transcript upstream_gene_variant - - - - - - DISTANCE=3302 rs1983070 3:135868204 T ENSESTG00000031311 ENSESTT00000078969 Transcript downstream_gene_variant - - - - - - DISTANCE=2844 rs1983070 3:135868204 T 55167 NM_018133.3 Transcript 3_prime_UTR_variant 4252 - - - - - rs1983070 3:135868204 T ENSESTG00000030943 ENSESTT00000077952 Transcript downstream_gene_variant - - - - - - DISTANCE=2667 rs1983070 3:135868204 T ENSESTG00000031311 ENSESTT00000079020 Transcript downstream_gene_variant - - - - - - DISTANCE=2740 rs1983070 3:135868204 T ENSESTG00000031311 ENSESTT00000078984 Transcript downstream_gene_variant - - - - - - DISTANCE=2850 rs1983070 3:135868204 T CCDS3087.1 CCDS3087.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4196 rs1983070 3:135868204 T CCDS33861.1 CCDS33861.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1785 rs1983070 3:135868204 T 5523 NM_001190447.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1452 rs1983070 3:135868204 T 55167 NM_001145417.1 Transcript 3_prime_UTR_variant 3451 - - - - - rs1983070 3:135868204 T ENSESTG00000030943 ENSESTT00000078030 Transcript downstream_gene_variant - - - - - - DISTANCE=3925 rs1983070 3:135868204 T CCDS3088.1 CCDS3088.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4196 rs1983070 3:135868204 T CCDS46922.1 CCDS46922.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1785 rs1983070 3:135868204 T 5523 NM_181897.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1452 rs1983070 3:135868204 T CCDS54642.1 CCDS54642.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4196 rs1983070 3:135868204 T 5523 NM_002718.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1452 rs1992952 3:135913665 G - ENSR00001374627 RegulatoryFeature regulatory_region_variant - - - - - - rs1992952 3:135913665 G ENSESTG00000031311 ENSESTT00000078992 Transcript intron_variant - - - - - - rs1992952 3:135913665 G ENSESTG00000031311 ENSESTT00000078976 Transcript intron_variant - - - - - - rs1992952 3:135913665 G CCDS33861.1 CCDS33861.1 Transcript intron_variant - - - - - - rs1992952 3:135913665 G ENSESTG00000031311 ENSESTT00000078969 Transcript intron_variant - - - - - - rs1992952 3:135913665 G 55167 NM_018133.3 Transcript intron_variant - - - - - - rs1992952 3:135913665 G 55167 NM_001145417.1 Transcript upstream_gene_variant - - - - - - DISTANCE=355 rs1992952 3:135913665 G ENSESTG00000031311 ENSESTT00000079020 Transcript intron_variant - - - - - - rs1992952 3:135913665 G ENSESTG00000031311 ENSESTT00000078984 Transcript intron_variant - - - - - - rs4678425 3:135924710 G - - - intergenic_variant - - - - - - rs661722 3:135953465 G - - - intergenic_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078360 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078394 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078333 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078312 Transcript intron_variant - - - - - - rs1279950 3:135996308 G 5096 NM_000532.4 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078469 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078447 Transcript intron_variant - - - - - - rs1279950 3:135996308 G 5096 NM_001178014.1 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078383 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078455 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078439 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078461 Transcript intron_variant - - - - - - rs1279950 3:135996308 G CCDS3089.1 CCDS3089.1 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078401 Transcript intron_variant - - - - - - rs1279950 3:135996308 G ENSESTG00000031060 ENSESTT00000078433 Transcript intron_variant - - - - - - rs1279950 3:135996308 G CCDS54643.1 CCDS54643.1 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078360 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078394 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078333 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078312 Transcript intron_variant - - - - - - rs552098 3:136037129 C 5096 NM_000532.4 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078469 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078447 Transcript intron_variant - - - - - - rs552098 3:136037129 C 5096 NM_001178014.1 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078383 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078455 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078439 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078461 Transcript intron_variant - - - - - - rs552098 3:136037129 C CCDS3089.1 CCDS3089.1 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078401 Transcript intron_variant - - - - - - rs552098 3:136037129 C ENSESTG00000031060 ENSESTT00000078433 Transcript intron_variant - - - - - - rs552098 3:136037129 C CCDS54643.1 CCDS54643.1 Transcript intron_variant - - - - - - rs477142 3:136060139 G CCDS3090.1 CCDS3090.1 Transcript intron_variant - - - - - - rs477142 3:136060139 G 10274 NM_005862.2 Transcript intron_variant - - - - - - rs1383752 3:136195525 C CCDS3090.1 CCDS3090.1 Transcript intron_variant - - - - - - rs1383752 3:136195525 C 10274 NM_005862.2 Transcript intron_variant - - - - - - rs1383752 3:136195525 C ENSESTG00000031188 ENSESTT00000078929 Transcript intron_variant - - - - - - rs1383752 3:136195525 C ENSESTG00000031188 ENSESTT00000078901 Transcript intron_variant - - - - - - rs6439645 3:136269438 C CCDS3090.1 CCDS3090.1 Transcript intron_variant - - - - - - rs6439645 3:136269438 C 10274 NM_005862.2 Transcript intron_variant - - - - - - rs6439645 3:136269438 C ENSESTG00000031188 ENSESTT00000078929 Transcript intron_variant - - - - - - rs6439645 3:136269438 C ENSESTG00000031188 ENSESTT00000078901 Transcript intron_variant - - - - - - rs7630773 3:136336628 G CCDS3090.1 CCDS3090.1 Transcript intron_variant - - - - - - rs7630773 3:136336628 G 10274 NM_005862.2 Transcript intron_variant - - - - - - rs7630773 3:136336628 G ENSESTG00000023323 ENSESTT00000058841 Transcript upstream_gene_variant - - - - - - DISTANCE=3023 rs7630773 3:136336628 G ENSESTG00000031188 ENSESTT00000078929 Transcript intron_variant - - - - - - rs7630773 3:136336628 G ENSESTG00000031188 ENSESTT00000078901 Transcript intron_variant - - - - - - rs6439648 3:136350672 A CCDS3090.1 CCDS3090.1 Transcript upstream_gene_variant - - - - - - DISTANCE=932 rs6439648 3:136350672 A ENSESTG00000023553 ENSESTT00000059402 Transcript intron_variant - - - - - - rs6439648 3:136350672 A 10274 NM_005862.2 Transcript intron_variant - - - - - - rs6439648 3:136350672 A ENSESTG00000031188 ENSESTT00000078929 Transcript intron_variant - - - - - - rs6439648 3:136350672 A ENSESTG00000031188 ENSESTT00000078901 Transcript intron_variant - - - - - - rs1292518 3:136504157 A ENSESTG00000023329 ENSESTT00000058868 Transcript synonymous_variant 343 141 47 E gaG/gaA - rs6439668 3:136540803 T 80723 NM_025246.2 Transcript intron_variant - - - - - - rs6439668 3:136540803 T 80723 NM_001097599.1 Transcript intron_variant - - - - - - rs6439668 3:136540803 T ENSESTG00000023352 ENSESTT00000058923 Transcript intron_variant - - - - - - rs6439668 3:136540803 T ENSESTG00000023352 ENSESTT00000058913 Transcript intron_variant - - - - - - rs6439668 3:136540803 T 80723 NM_001097600.1 Transcript intron_variant - - - - - - rs6439668 3:136540803 T ENSESTG00000023352 ENSESTT00000058927 Transcript intron_variant - - - - - - rs4678446 3:136543452 A 80723 NM_025246.2 Transcript intron_variant - - - - - - rs4678446 3:136543452 A 80723 NM_001097599.1 Transcript intron_variant - - - - - - rs4678446 3:136543452 A ENSESTG00000023352 ENSESTT00000058923 Transcript intron_variant - - - - - - rs4678446 3:136543452 A ENSESTG00000023352 ENSESTT00000058913 Transcript intron_variant - - - - - - rs4678446 3:136543452 A 80723 NM_001097600.1 Transcript intron_variant - - - - - - rs4678446 3:136543452 A ENSESTG00000023352 ENSESTT00000058927 Transcript intron_variant - - - - - - rs6784074 3:136612770 A - ENSR00001374746 RegulatoryFeature regulatory_region_variant - - - - - - rs6784074 3:136612770 A ENSESTG00000023376 ENSESTT00000059023 Transcript intron_variant - - - - - - rs6784074 3:136612770 A ENSESTG00000023376 ENSESTT00000059013 Transcript intron_variant - - - - - - rs6784074 3:136612770 A 4690 NM_006153.4 Transcript intron_variant - - - - - - rs12489085 3:136614125 G ENSESTG00000023376 ENSESTT00000059023 Transcript intron_variant - - - - - - rs12489085 3:136614125 G ENSESTG00000023376 ENSESTT00000059013 Transcript intron_variant - - - - - - rs12489085 3:136614125 G 4690 NM_006153.4 Transcript intron_variant - - - - - - rs2343661 3:136629324 C ENSESTG00000023376 ENSESTT00000059023 Transcript intron_variant - - - - - - rs2343661 3:136629324 C ENSESTG00000023376 ENSESTT00000059013 Transcript intron_variant - - - - - - rs2343661 3:136629324 C 4690 NM_006153.4 Transcript intron_variant - - - - - - rs1400265 3:136641650 A ENSESTG00000023376 ENSESTT00000059023 Transcript intron_variant - - - - - - rs1400265 3:136641650 A ENSESTG00000023376 ENSESTT00000059013 Transcript intron_variant - - - - - - rs1400265 3:136641650 A 4690 NM_006153.4 Transcript intron_variant - - - - - - rs6439676 3:136657363 G - ENSR00001483970 RegulatoryFeature regulatory_region_variant - - - - - - rs6439676 3:136657363 G ENSESTG00000023376 ENSESTT00000059013 Transcript intron_variant - - - - - - rs6439676 3:136657363 G CCDS54644.1 CCDS54644.1 Transcript intron_variant - - - - - - rs6439676 3:136657363 G 4690 NM_006153.4 Transcript intron_variant - - - - - - rs6439676 3:136657363 G CCDS3092.1 CCDS3092.1 Transcript intron_variant - - - - - - rs6439676 3:136657363 G 4690 NM_001190796.1 Transcript intron_variant - - - - - - rs3845926 3:136662140 C ENSESTG00000023376 ENSESTT00000059013 Transcript intron_variant - - - - - - rs3845926 3:136662140 C CCDS54644.1 CCDS54644.1 Transcript intron_variant - - - - - - rs3845926 3:136662140 C 4690 NM_006153.4 Transcript intron_variant - - - - - - rs3845926 3:136662140 C CCDS3092.1 CCDS3092.1 Transcript intron_variant - - - - - - rs3845926 3:136662140 C 4690 NM_001190796.1 Transcript intron_variant - - - - - - rs6772311 3:136680017 C - ENSR00001374773 RegulatoryFeature regulatory_region_variant - - - - - - rs6772311 3:136680017 C 53833 NM_144717.3 Transcript intron_variant - - - - - - rs6772311 3:136680017 C ENSESTG00000023419 ENSESTT00000059078 Transcript intron_variant - - - - - - rs6772311 3:136680017 C ENSESTG00000023468 ENSESTT00000059159 Transcript intron_variant - - - - - - rs6772311 3:136680017 C CCDS3093.1 CCDS3093.1 Transcript intron_variant - - - - - - rs1682360 3:136691531 G 53833 NM_144717.3 Transcript intron_variant - - - - - - rs1682360 3:136691531 G ENSESTG00000023419 ENSESTT00000059078 Transcript intron_variant - - - - - - rs1682360 3:136691531 G ENSESTG00000023468 ENSESTT00000059159 Transcript intron_variant - - - - - - rs1682360 3:136691531 G CCDS3093.1 CCDS3093.1 Transcript intron_variant - - - - - - rs13063556 3:136704046 C - ENSR00001483974 RegulatoryFeature regulatory_region_variant - - - - - - rs13063556 3:136704046 C 53833 NM_144717.3 Transcript intron_variant - - - - - - rs13063556 3:136704046 C ENSESTG00000023419 ENSESTT00000059078 Transcript intron_variant - - - - - - rs13063556 3:136704046 C ENSESTG00000023468 ENSESTT00000059159 Transcript upstream_gene_variant - - - - - - DISTANCE=3008 rs13063556 3:136704046 C CCDS3093.1 CCDS3093.1 Transcript intron_variant - - - - - - rs13063556 3:136704046 C ENSESTG00000023419 ENSESTT00000059143 Transcript intron_variant - - - - - - rs2628402 3:136721161 T 53833 NM_144717.3 Transcript intron_variant - - - - - - rs2628402 3:136721161 T CCDS3093.1 CCDS3093.1 Transcript intron_variant - - - - - - rs2628402 3:136721161 T ENSESTG00000023419 ENSESTT00000059143 Transcript intron_variant - - - - - - rs1824571 3:136930812 A - - - intergenic_variant - - - - - - rs9815723 3:136995085 A - - - intergenic_variant - - - - - - rs4678231 3:136995767 T - - - intergenic_variant - - - - - - rs7629332 3:137102431 G - - - intergenic_variant - - - - - - rs4592974 3:137124642 C - - - intergenic_variant - - - - - - rs7618310 3:137296143 T - - - intergenic_variant - - - - - - rs1596209 3:137303575 T - - - intergenic_variant - - - - - - rs1442613 3:137309956 C - - - intergenic_variant - - - - - - rs9851752 3:137313112 T - - - intergenic_variant - - - - - - rs4678358 3:137314105 C - - - intergenic_variant - - - - - - rs1946982 3:137315045 G - - - intergenic_variant - - - - - - rs7620412 3:137327835 C - - - intergenic_variant - - - - - - rs1111268 3:137333128 A - - - intergenic_variant - - - - - - rs1899447 3:137334102 A - - - intergenic_variant - - - - - - rs6766719 3:137334546 G - - - intergenic_variant - - - - - - rs6784542 3:137340115 G - - - intergenic_variant - - - - - - rs1540517 3:137350655 T - - - intergenic_variant - - - - - - rs201699 3:137464512 G - - - intergenic_variant - - - - - - rs201741 3:137510366 T - - - intergenic_variant - - - - - - rs201673 3:137520694 T - - - intergenic_variant - - - - - - rs3919806 3:137584559 A - - - intergenic_variant - - - - - - rs1867497 3:137680651 G - - - intergenic_variant - - - - - - rs168818 3:138077218 G 22808 NM_001252092.1 Transcript intron_variant - - - - - - rs168818 3:138077218 G ENSESTG00000028400 ENSESTT00000071529 Transcript intron_variant - - - - - - rs168818 3:138077218 G 22808 NM_001252091.1 Transcript intron_variant - - - - - - rs168818 3:138077218 G 22808 NM_001085049.2 Transcript intron_variant - - - - - - rs168818 3:138077218 G 22808 NM_001252090.1 Transcript intron_variant - - - - - - rs168818 3:138077218 G 22808 NM_001252093.1 Transcript intron_variant - - - - - - rs168818 3:138077218 G ENSESTG00000028400 ENSESTT00000071392 Transcript intron_variant - - - - - - rs168818 3:138077218 G ENSESTG00000028400 ENSESTT00000071492 Transcript intron_variant - - - - - - rs168818 3:138077218 G ENSESTG00000028400 ENSESTT00000071474 Transcript intron_variant - - - - - - rs168818 3:138077218 G ENSESTG00000028400 ENSESTT00000071483 Transcript intron_variant - - - - - - rs168818 3:138077218 G 22808 NM_012219.4 Transcript intron_variant - - - - - - rs1720834 3:138161433 T - ENSR00001374964 RegulatoryFeature regulatory_region_variant - - - - - - rs1720834 3:138161433 T ENSESTG00000028467 ENSESTT00000071632 Transcript intron_variant - - - - - - rs1720834 3:138161433 T CCDS3101.2 CCDS3101.2 Transcript intron_variant - - - - - - rs1720834 3:138161433 T ENSESTG00000028467 ENSESTT00000071643 Transcript intron_variant - - - - - - rs1720834 3:138161433 T 83850 NM_031913.3 Transcript intron_variant - - - - - - rs572238 3:140233957 T ENSESTG00000023103 ENSESTT00000058458 Transcript intron_variant - - - - - - rs572238 3:140233957 T 64084 NM_022131.2 Transcript intron_variant - - - - - - rs572238 3:140233957 T ENSESTG00000023103 ENSESTT00000058449 Transcript intron_variant - - - - - - rs572238 3:140233957 T CCDS3112.1 CCDS3112.1 Transcript intron_variant - - - - - - rs572238 3:140233957 T ENSESTG00000023103 ENSESTT00000058432 Transcript intron_variant - - - - - - rs1103645 3:140382848 A - - - intergenic_variant - - - - - - rs4334620 3:140512004 T - - - intergenic_variant - - - - - - rs1607492 3:140535754 A - - - intergenic_variant - - - - - - rs12492757 3:140587855 G - - - intergenic_variant - - - - - - rs2114515 3:140700374 A ENSESTG00000007504 ENSESTT00000018918 Transcript upstream_gene_variant - - - - - - DISTANCE=2331 rs2114515 3:140700374 A 55186 NM_001104647.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1589 rs2114515 3:140700374 A 55186 NM_018155.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1589 rs2114515 3:140700374 A ENSESTG00000007511 ENSESTT00000018925 Transcript upstream_gene_variant - - - - - - DISTANCE=4896 rs2114515 3:140700374 A ENSESTG00000012296 ENSESTT00000030854 Transcript downstream_gene_variant - - - - - - DISTANCE=4894 rs1346409 3:141104882 T ENSESTG00000012334 ENSESTT00000030950 Transcript intron_variant - - - - - - rs1346409 3:141104882 T 253461 NM_001080412.2 Transcript intron_variant - - - - - - rs1346409 3:141104882 T ENSESTG00000012334 ENSESTT00000030958 Transcript upstream_gene_variant - - - - - - DISTANCE=839 rs1346409 3:141104882 T ENSESTG00000012334 ENSESTT00000030953 Transcript upstream_gene_variant - - - - - - DISTANCE=402 rs1346409 3:141104882 T ENSESTG00000012334 ENSESTT00000030951 Transcript downstream_gene_variant - - - - - - DISTANCE=4551 rs1346409 3:141104882 T ENSESTG00000012334 ENSESTT00000030945 Transcript intron_variant - - - - - - rs9289633 3:141238554 C ENSESTG00000012393 ENSESTT00000031103 Transcript intron_variant - - - - - - rs9289633 3:141238554 C 5922 NM_006506.2 Transcript intron_variant - - - - - - rs9289633 3:141238554 C ENSESTG00000012393 ENSESTT00000031122 Transcript intron_variant - - - - - - rs9289633 3:141238554 C ENSESTG00000012393 ENSESTT00000031118 Transcript intron_variant - - - - - - rs9289633 3:141238554 C ENSESTG00000012393 ENSESTT00000031113 Transcript intron_variant - - - - - - rs9289633 3:141238554 C CCDS3117.1 CCDS3117.1 Transcript intron_variant - - - - - - rs9289633 3:141238554 C ENSESTG00000012393 ENSESTT00000031111 Transcript intron_variant - - - - - - rs9847956 3:141405558 G - ENSR00001484314 RegulatoryFeature regulatory_region_variant - - - - - - rs9847956 3:141405558 G ENSESTG00000021408 ENSESTT00000053727 Transcript downstream_gene_variant - - - - - - DISTANCE=1549 rs9847956 3:141405558 G 646730 XM_933859.6 Transcript intron_variant - - - - - - rs7644372 3:142035647 C 54464 NM_019001.3 Transcript intron_variant - - - - - - rs7644372 3:142035647 C 54464 NM_001042604.1 Transcript intron_variant - - - - - - rs7644372 3:142035647 C ENSESTG00000021737 ENSESTT00000054617 Transcript intron_variant - - - - - - rs7644372 3:142035647 C CCDS3123.1 CCDS3123.1 Transcript intron_variant - - - - - - rs7644372 3:142035647 C ENSESTG00000021737 ENSESTT00000054642 Transcript downstream_gene_variant - - - - - - DISTANCE=1839 rs6790042 3:142157744 C ENSESTG00000021620 ENSESTT00000054368 Transcript intron_variant - - - - - - rs6790042 3:142157744 C 54464 NM_019001.3 Transcript intron_variant - - - - - - rs6790042 3:142157744 C 54464 NM_001042604.1 Transcript intron_variant - - - - - - rs6790042 3:142157744 C CCDS3123.1 CCDS3123.1 Transcript intron_variant - - - - - - rs6790042 3:142157744 C ENSESTG00000021620 ENSESTT00000054395 Transcript intron_variant - - - - - - rs6790042 3:142157744 C ENSESTG00000021620 ENSESTT00000054380 Transcript intron_variant - - - - - - rs2049327 3:142337730 C - ENSR00001375600 RegulatoryFeature regulatory_region_variant - - - - - - rs2049327 3:142337730 C 5357 NM_001145319.1 Transcript intron_variant - - - - - - rs2049327 3:142337730 C 5357 NM_002670.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4536 rs2049327 3:142337730 C ENSESTG00000009658 ENSESTT00000024226 Transcript intron_variant - - - - - - rs2049327 3:142337730 C ENSESTG00000009658 ENSESTT00000024233 Transcript upstream_gene_variant - - - - - - DISTANCE=4536 rs2049327 3:142337730 C ENSESTG00000009658 ENSESTT00000024230 Transcript intron_variant - - - - - - rs2049327 3:142337730 C ENSESTG00000009658 ENSESTT00000024221 Transcript intron_variant - - - - - - rs1916640 3:142426832 C 5357 NM_001145319.1 Transcript intron_variant - - - - - - rs1916640 3:142426832 C 5357 NM_002670.2 Transcript intron_variant - - - - - - rs1916640 3:142426832 C ENSESTG00000009697 ENSESTT00000024303 Transcript intron_variant - - - - - - rs1916640 3:142426832 C 5357 NM_001172312.1 Transcript intron_variant - - - - - - rs1916640 3:142426832 C ENSESTG00000009697 ENSESTT00000024309 Transcript intron_variant - - - - - - rs1916640 3:142426832 C CCDS3125.1 CCDS3125.1 Transcript intron_variant - - - - - - rs10804688 3:143003017 A 285195 NM_173653.3 Transcript intron_variant - - - - - - rs10804688 3:143003017 A ENSESTG00000009857 ENSESTT00000024675 Transcript intron_variant - - - - - - rs10804688 3:143003017 A CCDS33872.1 CCDS33872.1 Transcript intron_variant - - - - - - rs10804688 3:143003017 A ENSESTG00000009857 ENSESTT00000024680 Transcript intron_variant - - - - - - rs6440171 3:143128757 A 285195 NM_173653.3 Transcript intron_variant - - - - - - rs6440171 3:143128757 A ENSESTG00000009857 ENSESTT00000024675 Transcript intron_variant - - - - - - rs6440171 3:143128757 A CCDS33872.1 CCDS33872.1 Transcript intron_variant - - - - - - rs6440171 3:143128757 A ENSESTG00000009857 ENSESTT00000024680 Transcript intron_variant - - - - - - rs1440728 3:143270569 T 285195 NM_173653.3 Transcript intron_variant - - - - - - rs1440728 3:143270569 T ENSESTG00000009857 ENSESTT00000024675 Transcript intron_variant - - - - - - rs1440728 3:143270569 T CCDS33872.1 CCDS33872.1 Transcript intron_variant - - - - - - rs1440728 3:143270569 T ENSESTG00000009857 ENSESTT00000024680 Transcript intron_variant - - - - - - rs6803069 3:143320463 G 285195 NM_173653.3 Transcript intron_variant - - - - - - rs6803069 3:143320463 G ENSESTG00000009857 ENSESTT00000024675 Transcript intron_variant - - - - - - rs6803069 3:143320463 G CCDS33872.1 CCDS33872.1 Transcript intron_variant - - - - - - rs6803069 3:143320463 G ENSESTG00000009857 ENSESTT00000024680 Transcript intron_variant - - - - - - rs6805323 3:143569251 A - ENSR00001375795 RegulatoryFeature regulatory_region_variant - - - - - - rs6805323 3:143569251 A 285195 NM_173653.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1878 rs6805323 3:143569251 A ENSESTG00000003132 ENSESTT00000007781 Transcript upstream_gene_variant - - - - - - DISTANCE=1930 rs6805323 3:143569251 A CCDS33872.1 CCDS33872.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2087 rs6805323 3:143569251 A ENSESTG00000003132 ENSESTT00000007788 Transcript upstream_gene_variant - - - - - - DISTANCE=1951 rs4396891 3:143621826 A - - - intergenic_variant - - - - - - rs1175949 3:143670548 A - ENSR00001375807 RegulatoryFeature regulatory_region_variant - - - - - - rs1175949 3:143670548 A - - - intergenic_variant - - - - - - rs1533558 3:144578006 T - - - intergenic_variant - - - - - - rs9817532 3:144624582 C - - - intergenic_variant - - - - - - rs2120984 3:144915440 C - - - intergenic_variant - - - - - - rs7630755 3:145521627 T - - - intergenic_variant - - - - - - rs10935585 3:145559317 A - - - intergenic_variant - - - - - - rs6786547 3:145652519 G - - - intergenic_variant - - - - - - rs544273 3:146218660 A 57047 NM_001199979.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4882 rs544273 3:146218660 A ENSESTG00000011087 ENSESTT00000027847 Transcript intron_variant - - - - - - rs544273 3:146218660 A ENSESTG00000011087 ENSESTT00000027902 Transcript upstream_gene_variant - - - - - - DISTANCE=4882 rs433452 3:146319552 G CCDS46931.1 CCDS46931.1 Transcript intron_variant - - - - - - rs433452 3:146319552 G 389158 NM_001085420.1 Transcript intron_variant - - - - - - rs1397885 3:146396747 C - - - intergenic_variant - - - - - - rs1502102 3:146829886 A - - - intergenic_variant - - - - - - rs4494896 3:147256219 G - - - intergenic_variant - - - - - - rs4681397 3:147904413 G - - - intergenic_variant - - - - - - rs4681410 3:148127392 A - - - intergenic_variant - - - - - - rs4681416 3:148183659 C - - - intergenic_variant - - - - - - rs7619366 3:148195821 C - - - intergenic_variant - - - - - - rs440881 3:148460467 A CCDS3137.1 CCDS3137.1 Transcript downstream_gene_variant - - - - - - DISTANCE=565 rs440881 3:148460467 A ENSESTG00000018334 ENSESTT00000046236 Transcript downstream_gene_variant - - - - - - DISTANCE=433 rs440881 3:148460467 A 185 NM_009585.3 Transcript 3_prime_UTR_variant 1949 - - - - - rs440881 3:148460467 A 185 NM_032049.3 Transcript 3_prime_UTR_variant 1907 - - - - - rs440881 3:148460467 A ENSESTG00000018334 ENSESTT00000046197 Transcript downstream_gene_variant - - - - - - DISTANCE=1317 rs440881 3:148460467 A ENSESTG00000018334 ENSESTT00000046227 Transcript downstream_gene_variant - - - - - - DISTANCE=433 rs440881 3:148460467 A 185 NM_000685.4 Transcript 3_prime_UTR_variant 2033 - - - - - rs440881 3:148460467 A 185 NM_004835.4 Transcript 3_prime_UTR_variant 2007 - - - - - rs440881 3:148460467 A ENSESTG00000018334 ENSESTT00000046185 Transcript downstream_gene_variant - - - - - - DISTANCE=1500 rs440881 3:148460467 A ENSESTG00000018334 ENSESTT00000046219 Transcript downstream_gene_variant - - - - - - DISTANCE=433 rs440881 3:148460467 A 185 NM_031850.3 Transcript 3_prime_UTR_variant 2091 - - - - - rs440881 3:148460467 A ENSESTG00000018334 ENSESTT00000046169 Transcript downstream_gene_variant - - - - - - DISTANCE=1181 rs2934129 3:148507120 A - ENSR00001484741 RegulatoryFeature regulatory_region_variant - - - - - - rs2934129 3:148507120 A - - - intergenic_variant - - - - - - rs773180 3:149000906 G - - - intergenic_variant - - - - - - rs1493262 3:149045910 T 116441 NM_138786.3 Transcript intron_variant - - - - - - rs1493262 3:149045910 T ENSESTG00000018903 ENSESTT00000047655 Transcript intron_variant - - - - - - rs1493262 3:149045910 T 116441 NM_001184723.1 Transcript intron_variant - - - - - - rs1493262 3:149045910 T CCDS3142.1 CCDS3142.1 Transcript intron_variant - - - - - - rs9823303 3:149887748 T - - - intergenic_variant - - - - - - rs1486791 3:149911663 A - - - intergenic_variant - - - - - - rs4681201 3:150045533 T - - - intergenic_variant - - - - - - rs4491924 3:150223636 T - - - intergenic_variant - - - - - - rs2870519 3:150945504 A - ENSR00001376764 RegulatoryFeature regulatory_region_variant - - - - - - rs2870519 3:150945504 A ENSESTG00000012959 ENSESTT00000032513 Transcript intron_variant - - - - - - rs2870519 3:150945504 A ENSESTG00000013007 ENSESTT00000032614 Transcript intron_variant - - - - - - rs2870519 3:150945504 A 9934 NM_014879.3 Transcript intron_variant - - - - - - rs2870519 3:150945504 A CCDS33876.1 CCDS33876.1 Transcript intron_variant - - - - - - rs2870519 3:150945504 A 9934 NM_001081455.1 Transcript intron_variant - - - - - - rs2870519 3:150945504 A 116931 NM_053002.4 Transcript intron_variant - - - - - - rs1401969 3:151510969 A - - - intergenic_variant - - - - - - rs399006 3:151951831 A - - - intergenic_variant - - - - - - rs1147310 3:152168964 C CCDS3164.1 CCDS3164.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C CCDS3167.1 CCDS3167.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C 4154 NM_207293.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C ENSESTG00000003886 ENSESTT00000009846 Transcript intron_variant - - - - - - rs1147310 3:152168964 C CCDS54656.1 CCDS54656.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C CCDS3168.1 CCDS3168.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C 4154 NM_207292.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C CCDS3166.1 CCDS3166.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C 4154 NM_207297.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C ENSESTG00000003886 ENSESTT00000009844 Transcript intron_variant - - - - - - rs1147310 3:152168964 C 4154 NM_207294.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C 4154 NM_207296.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C 4154 NM_021038.3 Transcript intron_variant - - - - - - rs1147310 3:152168964 C CCDS3165.1 CCDS3165.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C ENSESTG00000003886 ENSESTT00000009845 Transcript intron_variant - - - - - - rs1147310 3:152168964 C 4154 NM_207295.1 Transcript intron_variant - - - - - - rs1147310 3:152168964 C CCDS3163.1 CCDS3163.1 Transcript intron_variant - - - - - - rs7625139 3:152727438 A - - - intergenic_variant - - - - - - rs7355923 3:152841988 G - - - intergenic_variant - - - - - - rs12492975 3:153102467 A ENSESTG00000027783 ENSESTT00000069916 Transcript downstream_gene_variant - - - - - - DISTANCE=493 rs601930 3:153380942 G - - - intergenic_variant - - - - - - rs6440949 3:154346927 G - - - intergenic_variant - - - - - - rs4417828 3:154408674 A - - - intergenic_variant - - - - - - rs9289949 3:154427417 C - - - intergenic_variant - - - - - - rs6799342 3:154505112 G - - - intergenic_variant - - - - - - rs1534163 3:154688308 C ENSESTG00000000708 ENSESTT00000001694 Transcript upstream_gene_variant - - - - - - DISTANCE=296 rs1280064 3:154897074 G - ENSR00001377348 RegulatoryFeature regulatory_region_variant - - - - - - rs1280064 3:154897074 G 4311 NM_007288.2 Transcript intron_variant - - - - - - rs1280064 3:154897074 G ENSESTG00000000654 ENSESTT00000001577 Transcript upstream_gene_variant - - - - - - DISTANCE=1900 rs1280064 3:154897074 G ENSESTG00000000638 ENSESTT00000001571 Transcript intron_variant - - - - - - rs1280064 3:154897074 G CCDS3172.1 CCDS3172.1 Transcript intron_variant - - - - - - rs1280064 3:154897074 G 4311 NM_007289.2 Transcript intron_variant - - - - - - rs1280064 3:154897074 G 4311 NM_000902.3 Transcript intron_variant - - - - - - rs1280064 3:154897074 G 4311 NM_007287.2 Transcript intron_variant - - - - - - rs1280064 3:154897074 G ENSESTG00000000703 ENSESTT00000001688 Transcript intron_variant - - - - - - rs6766848 3:155097724 G ENSESTG00000000676 ENSESTT00000001622 Transcript intron_variant - - - - - - rs6441043 3:155891271 C 7881 NM_172160.2 Transcript intron_variant - - - - - - rs6441043 3:155891271 C CCDS3175.1 CCDS3175.1 Transcript intron_variant - - - - - - rs6441043 3:155891271 C CCDS3174.1 CCDS3174.1 Transcript intron_variant - - - - - - rs6441043 3:155891271 C 7881 NM_003471.3 Transcript intron_variant - - - - - - rs907061 3:156253562 C - ENSR00001485323 RegulatoryFeature regulatory_region_variant - - - - - - rs907061 3:156253562 C ENSESTG00000026096 ENSESTT00000065780 Transcript intron_variant - - - - - - rs907061 3:156253562 C ENSESTG00000004609 ENSESTT00000011625 Transcript downstream_gene_variant - - - - - - DISTANCE=4277 rs907061 3:156253562 C ENSESTG00000004609 ENSESTT00000011621 Transcript downstream_gene_variant - - - - - - DISTANCE=4277 rs907061 3:156253562 C CCDS3174.1 CCDS3174.1 Transcript intron_variant - - - - - - rs907061 3:156253562 C CCDS33882.1 CCDS33882.1 Transcript intron_variant - - - - - - rs907061 3:156253562 C 7881 NM_172159.3 Transcript intron_variant - - - - - - rs907061 3:156253562 C ENSESTG00000026525 ENSESTT00000066917 Transcript downstream_gene_variant - - - - - - DISTANCE=4374 rs907061 3:156253562 C 7881 NM_172160.2 Transcript intron_variant - - - - - - rs907061 3:156253562 C 7881 NM_003471.3 Transcript intron_variant - - - - - - rs907061 3:156253562 C CCDS3175.1 CCDS3175.1 Transcript intron_variant - - - - - - rs907061 3:156253562 C 6747 NM_007107.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4367 rs344021 3:156495672 C ENSESTG00000026496 ENSESTT00000066757 Transcript intron_variant - - - - - - rs344021 3:156495672 C 730091 NR_038387.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1032043 3:156746786 G 389170 NM_001004316.2 Transcript intron_variant - - - - - - rs2722375 3:157344247 A - - - intergenic_variant - - - - - - rs2247915 3:158392803 C ENSESTG00000004677 ENSESTT00000011893 Transcript intron_variant - - - - - - rs2247915 3:158392803 C 56925 NM_020169.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2321 rs2247915 3:158392803 C ENSESTG00000004677 ENSESTT00000011883 Transcript intron_variant - - - - - - rs2247915 3:158392803 C CCDS3183.1 CCDS3183.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2536 rs2247915 3:158392803 C ENSESTG00000004762 ENSESTT00000012076 Transcript upstream_gene_variant - - - - - - DISTANCE=2633 rs2247915 3:158392803 C ENSESTG00000004677 ENSESTT00000011897 Transcript intron_variant - - - - - - rs2247915 3:158392803 C CCDS33885.1 CCDS33885.1 Transcript intron_variant - - - - - - rs2247915 3:158392803 C ENSESTG00000004677 ENSESTT00000011875 Transcript intron_variant - - - - - - rs2247915 3:158392803 C 85476 NM_024996.5 Transcript intron_variant - - - - - - rs2621311 3:159023947 C CCDS56292.1 CCDS56292.1 Transcript intron_variant - - - - - - rs2621311 3:159023947 C 29970 NM_001197108.1 Transcript intron_variant - - - - - - rs2621311 3:159023947 C CCDS56293.1 CCDS56293.1 Transcript intron_variant - - - - - - rs2621311 3:159023947 C 100505385 NM_001197114.1 Transcript intron_variant - - - - - - rs2621311 3:159023947 C CCDS3186.1 CCDS3186.1 Transcript intron_variant - - - - - - rs2621311 3:159023947 C 29970 NM_014575.3 Transcript intron_variant - - - - - - rs2621311 3:159023947 C CCDS56291.1 CCDS56291.1 Transcript intron_variant - - - - - - rs2621311 3:159023947 C 29970 NM_001197107.1 Transcript intron_variant - - - - - - rs2621311 3:159023947 C 100505385 NM_001197113.1 Transcript intron_variant - - - - - - rs2621311 3:159023947 C CCDS56289.1 CCDS56289.1 Transcript intron_variant - - - - - - rs1449014 3:159105822 A CCDS56292.1 CCDS56292.1 Transcript intron_variant - - - - - - rs1449014 3:159105822 A 29970 NM_001197108.1 Transcript intron_variant - - - - - - rs1449014 3:159105822 A CCDS56293.1 CCDS56293.1 Transcript intron_variant - - - - - - rs1449014 3:159105822 A 100505385 NM_001197114.1 Transcript intron_variant - - - - - - rs1449014 3:159105822 A CCDS3186.1 CCDS3186.1 Transcript intron_variant - - - - - - rs1449014 3:159105822 A 29970 NM_014575.3 Transcript intron_variant - - - - - - rs1449014 3:159105822 A CCDS56291.1 CCDS56291.1 Transcript intron_variant - - - - - - rs1449014 3:159105822 A 29970 NM_001197107.1 Transcript intron_variant - - - - - - rs1449014 3:159105822 A 100505385 NM_001197113.1 Transcript intron_variant - - - - - - rs1449014 3:159105822 A CCDS56289.1 CCDS56289.1 Transcript intron_variant - - - - - - rs1489921 3:159180660 T CCDS56292.1 CCDS56292.1 Transcript intron_variant - - - - - - rs1489921 3:159180660 T 29970 NM_001197108.1 Transcript intron_variant - - - - - - rs1489921 3:159180660 T CCDS56293.1 CCDS56293.1 Transcript intron_variant - - - - - - rs1489921 3:159180660 T 100505385 NM_001197114.1 Transcript intron_variant - - - - - - rs1489921 3:159180660 T CCDS3186.1 CCDS3186.1 Transcript intron_variant - - - - - - rs1489921 3:159180660 T 29970 NM_014575.3 Transcript intron_variant - - - - - - rs1489921 3:159180660 T CCDS56291.1 CCDS56291.1 Transcript intron_variant - - - - - - rs1489921 3:159180660 T 29970 NM_001197107.1 Transcript intron_variant - - - - - - rs1489921 3:159180660 T 100505385 NM_001197113.1 Transcript intron_variant - - - - - - rs1489921 3:159180660 T CCDS56289.1 CCDS56289.1 Transcript intron_variant - - - - - - rs632105 3:159724491 G - ENSR00001485594 RegulatoryFeature regulatory_region_variant - - - - - - rs632105 3:159724491 G - - - intergenic_variant - - - - - - rs4680574 3:159973857 A ENSESTG00000031670 ENSESTT00000080089 Transcript intron_variant - - - - - - rs4680574 3:159973857 A 57560 NM_020800.2 Transcript downstream_gene_variant - - - - - - DISTANCE=917 rs4680574 3:159973857 A ENSESTG00000031670 ENSESTT00000080265 Transcript downstream_gene_variant - - - - - - DISTANCE=2114 rs4680574 3:159973857 A ENSESTG00000031670 ENSESTT00000080096 Transcript downstream_gene_variant - - - - - - DISTANCE=2114 rs4680574 3:159973857 A ENSESTG00000031670 ENSESTT00000080024 Transcript intron_variant - - - - - - rs4680574 3:159973857 A CCDS54668.1 CCDS54668.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2456 rs4680574 3:159973857 A ENSESTG00000031670 ENSESTT00000080216 Transcript intron_variant - - - - - - rs4680574 3:159973857 A ENSESTG00000031670 ENSESTT00000080039 Transcript downstream_gene_variant - - - - - - DISTANCE=2114 rs4680574 3:159973857 A CCDS3188.1 CCDS3188.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2456 rs4680574 3:159973857 A 57560 NM_001190242.1 Transcript downstream_gene_variant - - - - - - DISTANCE=917 rs4680574 3:159973857 A ENSESTG00000031670 ENSESTT00000080228 Transcript downstream_gene_variant - - - - - - DISTANCE=2114 rs4680574 3:159973857 A 57560 NM_001190241.1 Transcript downstream_gene_variant - - - - - - DISTANCE=917 rs1953507 3:160049926 C ENSESTG00000031670 ENSESTT00000080089 Transcript intron_variant - - - - - - rs1953507 3:160049926 C 57560 NM_020800.2 Transcript intron_variant - - - - - - rs1953507 3:160049926 C ENSESTG00000031670 ENSESTT00000080102 Transcript intron_variant - - - - - - rs1953507 3:160049926 C ENSESTG00000031670 ENSESTT00000080096 Transcript intron_variant - - - - - - rs1953507 3:160049926 C ENSESTG00000031670 ENSESTT00000080024 Transcript intron_variant - - - - - - rs1953507 3:160049926 C CCDS54668.1 CCDS54668.1 Transcript intron_variant - - - - - - rs1953507 3:160049926 C ENSESTG00000031670 ENSESTT00000080216 Transcript intron_variant - - - - - - rs1953507 3:160049926 C ENSESTG00000031670 ENSESTT00000080039 Transcript intron_variant - - - - - - rs1953507 3:160049926 C CCDS3188.1 CCDS3188.1 Transcript intron_variant - - - - - - rs1953507 3:160049926 C ENSESTG00000031670 ENSESTT00000080237 Transcript intron_variant - - - - - - rs1953507 3:160049926 C 57560 NM_001190242.1 Transcript intron_variant - - - - - - rs1953507 3:160049926 C ENSESTG00000031670 ENSESTT00000080228 Transcript intron_variant - - - - - - rs1953507 3:160049926 C 57560 NM_001190241.1 Transcript intron_variant - - - - - - rs1953507 3:160049926 C ENSESTG00000031670 ENSESTT00000080047 Transcript intron_variant - - - - - - rs6776552 3:160389299 C - ENSR00001378208 RegulatoryFeature regulatory_region_variant - - - - - - rs6776552 3:160389299 C - - - intergenic_variant - - - - - - rs1447628 3:160625882 A 151742 NM_139245.2 Transcript intron_variant - - - - - - rs1447628 3:160625882 A CCDS33886.1 CCDS33886.1 Transcript intron_variant - - - - - - rs1839013 3:160686777 A - ENSR00001378249 RegulatoryFeature regulatory_region_variant - - - - - - rs1839013 3:160686777 A 151742 NM_139245.2 Transcript intron_variant - - - - - - rs1839013 3:160686777 A CCDS33886.1 CCDS33886.1 Transcript intron_variant - - - - - - rs339121 3:161145319 G - - - intergenic_variant - - - - - - rs339110 3:161197477 C - - - intergenic_variant - - - - - - rs1601200 3:161212352 C ENSESTG00000027501 ENSESTT00000069223 Transcript upstream_gene_variant - - - - - - DISTANCE=2549 rs1601200 3:161212352 C 131149 NM_001080440.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2244 rs1601200 3:161212352 C ENSESTG00000027501 ENSESTT00000069215 Transcript upstream_gene_variant - - - - - - DISTANCE=2464 rs1601200 3:161212352 C CCDS46948.1 CCDS46948.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2244 rs7653878 3:161257643 G ENSESTG00000027501 ENSESTT00000069215 Transcript intron_variant - - - - - - rs6441388 3:161291512 C ENSESTG00000027501 ENSESTT00000069215 Transcript intron_variant - - - - - - rs1911118 3:161306205 T - - - intergenic_variant - - - - - - rs7429212 3:162361380 G - - - intergenic_variant - - - - - - rs9283620 3:162654594 C - - - intergenic_variant - - - - - - rs9875440 3:162708811 C - - - intergenic_variant - - - - - - rs11706076 3:162761748 C - - - intergenic_variant - - - - - - rs7645908 3:162827118 G - - - intergenic_variant - - - - - - rs1907662 3:162933851 T ENSESTG00000024864 ENSESTT00000062824 Transcript downstream_gene_variant - - - - - - DISTANCE=3851 rs1907662 3:162933851 T ENSESTG00000024864 ENSESTT00000062817 Transcript downstream_gene_variant - - - - - - DISTANCE=2997 rs1907662 3:162933851 T ENSESTG00000024864 ENSESTT00000062797 Transcript intron_variant - - - - - - rs1907662 3:162933851 T ENSESTG00000024864 ENSESTT00000062774 Transcript downstream_gene_variant - - - - - - DISTANCE=4037 rs1907662 3:162933851 T 647107 NR_033945.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1907662 3:162933851 T ENSESTG00000024864 ENSESTT00000062868 Transcript intron_variant - - - - - - rs4613457 3:163992856 T - - - intergenic_variant - - - - - - rs7622779 3:164116856 T - - - intergenic_variant - - - - - - rs2643160 3:164412844 T - - - intergenic_variant - - - - - - rs2688427 3:165399333 C - - - intergenic_variant - - - - - - rs996055 3:165889439 C - - - intergenic_variant - - - - - - rs1403094 3:167806221 T - ENSR00001378724 RegulatoryFeature regulatory_region_variant - - - - - - rs1403094 3:167806221 T 27333 NM_014498.3 Transcript intron_variant - - - - - - rs1403094 3:167806221 T ENSESTG00000009184 ENSESTT00000023045 Transcript intron_variant - - - - - - rs1403094 3:167806221 T ENSESTG00000009184 ENSESTT00000023036 Transcript intron_variant - - - - - - rs1403094 3:167806221 T CCDS3204.1 CCDS3204.1 Transcript intron_variant - - - - - - rs4955611 3:168361716 T ENSESTG00000024312 ENSESTT00000061488 Transcript intron_variant - - - - - - rs4955611 3:168361716 T 93556 NR_021485.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs9843139 3:168563853 T - - - intergenic_variant - - - - - - rs1274088 3:169019047 A 2122 NM_001205194.1 Transcript intron_variant - - - - - - rs1274088 3:169019047 A 2122 NM_004991.3 Transcript intron_variant - - - - - - rs1273879 3:169106036 C - ENSR00001378892 RegulatoryFeature regulatory_region_variant - - - - - - rs1273879 3:169106036 C 2122 NM_001205194.1 Transcript intron_variant - - - - - - rs1273879 3:169106036 C 2122 NM_004991.3 Transcript intron_variant - - - - - - rs1920118 3:169581550 G - ENSR00001485902 RegulatoryFeature regulatory_region_variant - - - - - - rs1920118 3:169581550 G 79782 NM_024727.2 Transcript intron_variant - - - - - - rs1920118 3:169581550 G CCDS43167.1 CCDS43167.1 Transcript intron_variant - - - - - - rs6444887 3:169749108 G - - - intergenic_variant - - - - - - rs7650645 3:169782735 C ENSESTG00000007776 ENSESTT00000019638 Transcript downstream_gene_variant - - - - - - DISTANCE=1679 rs7650645 3:169782735 C ENSESTG00000007758 ENSESTT00000019605 Transcript intron_variant - - - - - - rs7650645 3:169782735 C 26996 NM_014373.2 Transcript intron_variant - - - - - - rs7650645 3:169782735 C ENSESTG00000007758 ENSESTT00000019599 Transcript intron_variant - - - - - - rs7650645 3:169782735 C ENSESTG00000007758 ENSESTT00000019612 Transcript intron_variant - - - - - - rs7650645 3:169782735 C ENSESTG00000007776 ENSESTT00000019641 Transcript 3_prime_UTR_variant 247 - - - - - rs7650645 3:169782735 C ENSESTG00000007758 ENSESTT00000019627 Transcript intron_variant - - - - - - rs7650645 3:169782735 C ENSESTG00000007758 ENSESTT00000019618 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082283 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082248 Transcript intron_variant - - - - - - rs1875094 3:170804501 C CCDS54673.1 CCDS54673.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C 23043 NM_001161563.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082264 Transcript intron_variant - - - - - - rs1875094 3:170804501 C CCDS54674.1 CCDS54674.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C 23043 NM_015028.2 Transcript intron_variant - - - - - - rs1875094 3:170804501 C CCDS54676.1 CCDS54676.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C 23043 NM_001161562.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082243 Transcript intron_variant - - - - - - rs1875094 3:170804501 C CCDS54678.1 CCDS54678.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C CCDS54679.1 CCDS54679.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C CCDS54677.1 CCDS54677.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082296 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082293 Transcript intron_variant - - - - - - rs1875094 3:170804501 C 23043 NM_001161566.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082308 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082275 Transcript intron_variant - - - - - - rs1875094 3:170804501 C 23043 NM_001161565.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082287 Transcript intron_variant - - - - - - rs1875094 3:170804501 C CCDS46956.1 CCDS46956.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082314 Transcript intron_variant - - - - - - rs1875094 3:170804501 C 23043 NM_001161561.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082252 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082254 Transcript intron_variant - - - - - - rs1875094 3:170804501 C 23043 NM_001161564.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C CCDS54675.1 CCDS54675.1 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082304 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082279 Transcript intron_variant - - - - - - rs1875094 3:170804501 C ENSESTG00000032543 ENSESTT00000082261 Transcript intron_variant - - - - - - rs1875094 3:170804501 C 23043 NM_001161560.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C CCDS54673.1 CCDS54673.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C 23043 NM_001161563.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C CCDS54674.1 CCDS54674.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C 23043 NM_015028.2 Transcript intron_variant - - - - - - rs6444978 3:171036459 C CCDS54676.1 CCDS54676.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C 23043 NM_001161562.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C CCDS54678.1 CCDS54678.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C CCDS54679.1 CCDS54679.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C CCDS54677.1 CCDS54677.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C ENSESTG00000032502 ENSESTT00000082080 Transcript intron_variant - - - - - - rs6444978 3:171036459 C 23043 NM_001161566.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C 23043 NM_001161565.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C CCDS46956.1 CCDS46956.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C 23043 NM_001161561.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C 23043 NM_001161564.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C CCDS54675.1 CCDS54675.1 Transcript intron_variant - - - - - - rs6444978 3:171036459 C 23043 NM_001161560.1 Transcript intron_variant - - - - - - rs6764335 3:171572483 T CCDS46958.1 CCDS46958.1 Transcript intron_variant - - - - - - rs6764335 3:171572483 T ENSESTG00000032283 ENSESTT00000081477 Transcript downstream_gene_variant - - - - - - DISTANCE=847 rs6764335 3:171572483 T 389177 NM_001164436.1 Transcript intron_variant - - - - - - rs1392113 3:172612614 A ENSESTG00000033832 ENSESTT00000085538 Transcript intron_variant - - - - - - rs1392113 3:172612614 A ENSESTG00000033832 ENSESTT00000085541 Transcript intron_variant - - - - - - rs1392113 3:172612614 A CCDS3221.1 CCDS3221.1 Transcript intron_variant - - - - - - rs1392113 3:172612614 A 83893 NM_031955.5 Transcript intron_variant - - - - - - rs1515436 3:172699317 A CCDS3221.1 CCDS3221.1 Transcript intron_variant - - - - - - rs1515436 3:172699317 A 83893 NM_031955.5 Transcript intron_variant - - - - - - rs1515436 3:172699317 A ENSESTG00000033825 ENSESTT00000085522 Transcript intron_variant - - - - - - rs524476 3:172787873 A CCDS3221.1 CCDS3221.1 Transcript intron_variant - - - - - - rs524476 3:172787873 A 83893 NM_031955.5 Transcript intron_variant - - - - - - rs524476 3:172787873 A ENSESTG00000033825 ENSESTT00000085522 Transcript intron_variant - - - - - - rs792129 3:172933635 G - - - intergenic_variant - - - - - - rs13062588 3:173785992 A 22871 NM_014932.2 Transcript intron_variant - - - - - - rs13062588 3:173785992 A CCDS3222.1 CCDS3222.1 Transcript intron_variant - - - - - - rs12696347 3:173786009 C 22871 NM_014932.2 Transcript intron_variant - - - - - - rs12696347 3:173786009 C CCDS3222.1 CCDS3222.1 Transcript intron_variant - - - - - - rs13062959 3:173786213 T 22871 NM_014932.2 Transcript intron_variant - - - - - - rs13062959 3:173786213 T CCDS3222.1 CCDS3222.1 Transcript intron_variant - - - - - - rs4472054 3:174661107 T 254827 NM_207015.2 Transcript intron_variant - - - - - - rs4472054 3:174661107 T CCDS46960.1 CCDS46960.1 Transcript intron_variant - - - - - - rs2861902 3:174701236 C 254827 NM_207015.2 Transcript intron_variant - - - - - - rs2861902 3:174701236 C CCDS46960.1 CCDS46960.1 Transcript intron_variant - - - - - - rs4585208 3:174733958 T 254827 NM_207015.2 Transcript intron_variant - - - - - - rs4585208 3:174733958 T CCDS46960.1 CCDS46960.1 Transcript intron_variant - - - - - - rs2862405 3:175725121 A - - - intergenic_variant - - - - - - rs857667 3:176356184 A ENSESTG00000030365 ENSESTT00000076422 Transcript upstream_gene_variant - - - - - - DISTANCE=2864 rs1905495 3:176721591 T - - - intergenic_variant - - - - - - rs1201300 3:176765253 A CCDS46961.1 CCDS46961.1 Transcript intron_variant - - - - - - rs1201300 3:176765253 A ENSESTG00000030291 ENSESTT00000076313 Transcript downstream_gene_variant - - - - - - DISTANCE=4129 rs1201300 3:176765253 A ENSESTG00000030291 ENSESTT00000076369 Transcript downstream_gene_variant - - - - - - DISTANCE=4150 rs1201300 3:176765253 A ENSESTG00000030291 ENSESTT00000076346 Transcript downstream_gene_variant - - - - - - DISTANCE=2580 rs1201300 3:176765253 A ENSESTG00000030291 ENSESTT00000076290 Transcript downstream_gene_variant - - - - - - DISTANCE=4092 rs1201300 3:176765253 A 79718 NM_024665.4 Transcript intron_variant - - - - - - rs1201300 3:176765253 A ENSESTG00000030291 ENSESTT00000076402 Transcript downstream_gene_variant - - - - - - DISTANCE=4229 rs4857684 3:177100695 C - - - intergenic_variant - - - - - - rs6800033 3:177188292 C - ENSR00001380231 RegulatoryFeature regulatory_region_variant - - - - - - rs6800033 3:177188292 C 100505566 NR_047568.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6800033 3:177188292 C ENSESTG00000008493 ENSESTT00000021402 Transcript intron_variant - - - - - - rs4241482 3:177279403 A 100505566 NR_047568.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4241482 3:177279403 A ENSESTG00000008493 ENSESTT00000021402 Transcript intron_variant - - - - - - rs6443483 3:177444501 C 100505566 NR_047568.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6443483 3:177444501 C ENSESTG00000008493 ENSESTT00000021402 Transcript intron_variant - - - - - - rs6443483 3:177444501 C ENSESTG00000008493 ENSESTT00000021403 Transcript intron_variant - - - - - - rs4857646 3:178215002 G - ENSR00001486472 RegulatoryFeature regulatory_region_variant - - - - - - rs4857646 3:178215002 G - - - intergenic_variant - - - - - - rs4855006 3:179019756 C - ENSR00001380559 RegulatoryFeature regulatory_region_variant - - - - - - rs4855006 3:179019756 C - - - intergenic_variant - - - - - - rs7637065 3:179096508 G ENSESTG00000016609 ENSESTT00000041686 Transcript 5_prime_UTR_variant 191 - - - - - rs7637065 3:179096508 G 55669 NM_033540.2 Transcript missense_variant 1694 1568 523 P/R cCt/cGt - PolyPhen=benign;SIFT=tolerated rs7637065 3:179096508 G CCDS3228.1 CCDS3228.1 Transcript missense_variant 1568 1568 523 P/R cCt/cGt - PolyPhen=benign;SIFT=tolerated rs7637065 3:179096508 G ENSESTG00000016584 ENSESTT00000041601 Transcript downstream_gene_variant - - - - - - DISTANCE=350 rs7637065 3:179096508 G ENSESTG00000016584 ENSESTT00000041626 Transcript downstream_gene_variant - - - - - - DISTANCE=1172 rs6443668 3:179438418 G ENSESTG00000027305 ENSESTT00000068946 Transcript intron_variant - - - - - - rs6443668 3:179438418 G 8975 NM_003940.2 Transcript intron_variant - - - - - - rs6443668 3:179438418 G ENSESTG00000027305 ENSESTT00000068960 Transcript intron_variant - - - - - - rs6443668 3:179438418 G ENSESTG00000027305 ENSESTT00000068971 Transcript intron_variant - - - - - - rs6443668 3:179438418 G CCDS3235.1 CCDS3235.1 Transcript intron_variant - - - - - - rs6443668 3:179438418 G ENSESTG00000027305 ENSESTT00000068914 Transcript intron_variant - - - - - - rs1518861 3:180471487 T - - - intergenic_variant - - - - - - rs3849429 3:180802734 G - - - intergenic_variant - - - - - - rs6414492 3:181359218 T ENSESTG00000015361 ENSESTT00000038498 Transcript intron_variant - - - - - - rs6414492 3:181359218 T ENSESTG00000015361 ENSESTT00000038501 Transcript intron_variant - - - - - - rs6414492 3:181359218 T 347689 NR_004053.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs6414492 3:181359218 T ENSESTG00000015361 ENSESTT00000038492 Transcript intron_variant - - - - - - rs6414492 3:181359218 T ENSESTG00000015361 ENSESTT00000038463 Transcript intron_variant - - - - - - rs9860346 3:181398230 C ENSESTG00000015361 ENSESTT00000038498 Transcript intron_variant - - - - - - rs9860346 3:181398230 C ENSESTG00000015361 ENSESTT00000038501 Transcript intron_variant - - - - - - rs9860346 3:181398230 C 347689 NR_004053.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs9860346 3:181398230 C ENSESTG00000015361 ENSESTT00000038492 Transcript intron_variant - - - - - - rs9877831 3:182009866 C - - - intergenic_variant - - - - - - rs3108738 3:182392776 A - - - intergenic_variant - - - - - - rs1039791 3:183122296 A CCDS3243.1 CCDS3243.1 Transcript intron_variant - - - - - - rs1039791 3:183122296 A ENSESTG00000035149 ENSESTT00000088816 Transcript intron_variant - - - - - - rs1039791 3:183122296 A ENSESTG00000026636 ENSESTT00000067102 Transcript intron_variant - - - - - - rs1039791 3:183122296 A ENSESTG00000035149 ENSESTT00000088818 Transcript upstream_gene_variant - - - - - - DISTANCE=3969 rs1039791 3:183122296 A 23101 NM_015078.2 Transcript intron_variant - - - - - - rs1039791 3:183122296 A ENSESTG00000026636 ENSESTT00000067145 Transcript intron_variant - - - - - - rs9290760 3:183295490 T - ENSR00001486764 RegulatoryFeature regulatory_region_variant - - - - - - rs9290760 3:183295490 T ENSESTG00000034645 ENSESTT00000087587 Transcript upstream_gene_variant - - - - - - DISTANCE=2753 rs6443900 3:183340634 C - - - intergenic_variant - - - - - - rs7627110 3:184834888 A ENSESTG00000002199 ENSESTT00000005503 Transcript intron_variant - - - - - - rs7627110 3:184834888 A CCDS33900.1 CCDS33900.1 Transcript intron_variant - - - - - - rs7627110 3:184834888 A 285382 NM_001025266.1 Transcript intron_variant - - - - - - rs3114675 3:185248918 A ENSESTG00000025852 ENSESTT00000065180 Transcript downstream_gene_variant - - - - - - DISTANCE=2506 rs3114675 3:185248918 A ENSESTG00000025852 ENSESTT00000065196 Transcript downstream_gene_variant - - - - - - DISTANCE=3632 rs3114675 3:185248918 A ENSESTG00000026079 ENSESTT00000065719 Transcript intron_variant - - - - - - rs3114675 3:185248918 A 200879 NM_139248.2 Transcript intron_variant - - - - - - rs3114675 3:185248918 A CCDS3272.1 CCDS3272.1 Transcript intron_variant - - - - - - rs476011 3:185279963 C - ENSR00001381551 RegulatoryFeature regulatory_region_variant - - - - - - rs476011 3:185279963 C - - - intergenic_variant - - - - - - rs6444079 3:185358721 C 10644 NM_006548.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2806 rs6444079 3:185358721 C ENSESTG00000025749 ENSESTT00000065120 Transcript downstream_gene_variant - - - - - - DISTANCE=4631 rs6444079 3:185358721 C CCDS33903.1 CCDS33903.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4598 rs6444079 3:185358721 C 10644 NM_001007225.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2806 rs6444079 3:185358721 C ENSESTG00000025749 ENSESTT00000065088 Transcript downstream_gene_variant - - - - - - DISTANCE=4631 rs6444079 3:185358721 C ENSESTG00000025749 ENSESTT00000065083 Transcript downstream_gene_variant - - - - - - DISTANCE=4631 rs6444079 3:185358721 C CCDS3273.2 CCDS3273.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4598 rs9809821 3:185449215 G 10644 NM_006548.4 Transcript intron_variant - - - - - - rs9809821 3:185449215 G ENSESTG00000025749 ENSESTT00000065109 Transcript intron_variant - - - - - - rs9809821 3:185449215 G CCDS33903.1 CCDS33903.1 Transcript intron_variant - - - - - - rs9809821 3:185449215 G 10644 NM_001007225.1 Transcript intron_variant - - - - - - rs9809821 3:185449215 G ENSESTG00000025749 ENSESTT00000065088 Transcript intron_variant - - - - - - rs9809821 3:185449215 G ENSESTG00000025749 ENSESTT00000065083 Transcript intron_variant - - - - - - rs9809821 3:185449215 G CCDS3273.2 CCDS3273.2 Transcript intron_variant - - - - - - rs6444100 3:185720020 C - - - intergenic_variant - - - - - - rs6788623 3:185732804 G - - - intergenic_variant - - - - - - rs7639389 3:185740217 T - - - intergenic_variant - - - - - - rs4686723 3:185753352 T - ENSR00001381714 RegulatoryFeature regulatory_region_variant - - - - - - rs4686723 3:185753352 T - - - intergenic_variant - - - - - - rs5001711 3:185773758 A ENSESTG00000025552 ENSESTT00000064770 Transcript intron_variant - - - - - - rs5001711 3:185773758 A ENSESTG00000025552 ENSESTT00000064687 Transcript intron_variant - - - - - - rs5001711 3:185773758 A ENSESTG00000025552 ENSESTT00000064672 Transcript intron_variant - - - - - - rs5001711 3:185773758 A ENSESTG00000025552 ENSESTT00000064739 Transcript intron_variant - - - - - - rs5001711 3:185773758 A ENSESTG00000025552 ENSESTT00000064692 Transcript intron_variant - - - - - - rs5001711 3:185773758 A CCDS33906.1 CCDS33906.1 Transcript intron_variant - - - - - - rs5001711 3:185773758 A 2119 NM_004454.2 Transcript intron_variant - - - - - - rs13073156 3:185879296 C ENSESTG00000025517 ENSESTT00000064399 Transcript intron_variant - - - - - - rs13073156 3:185879296 C 1608 NM_001080745.1 Transcript intron_variant - - - - - - rs13073156 3:185879296 C 1608 NM_001346.2 Transcript intron_variant - - - - - - rs13073156 3:185879296 C CCDS43181.1 CCDS43181.1 Transcript intron_variant - - - - - - rs13073156 3:185879296 C 1608 NM_001080744.1 Transcript intron_variant - - - - - - rs13073156 3:185879296 C CCDS3274.1 CCDS3274.1 Transcript intron_variant - - - - - - rs13073156 3:185879296 C CCDS43182.1 CCDS43182.1 Transcript intron_variant - - - - - - rs13077618 3:185892566 C ENSESTG00000025517 ENSESTT00000064399 Transcript intron_variant - - - - - - rs13077618 3:185892566 C 1608 NM_001080745.1 Transcript intron_variant - - - - - - rs13077618 3:185892566 C 1608 NM_001346.2 Transcript intron_variant - - - - - - rs13077618 3:185892566 C CCDS43181.1 CCDS43181.1 Transcript intron_variant - - - - - - rs13077618 3:185892566 C 1608 NM_001080744.1 Transcript intron_variant - - - - - - rs13077618 3:185892566 C CCDS3274.1 CCDS3274.1 Transcript intron_variant - - - - - - rs13077618 3:185892566 C CCDS43182.1 CCDS43182.1 Transcript intron_variant - - - - - - rs759672 3:185928970 G ENSESTG00000025517 ENSESTT00000064399 Transcript intron_variant - - - - - - rs759672 3:185928970 G 1608 NM_001080745.1 Transcript intron_variant - - - - - - rs759672 3:185928970 G 1608 NM_001346.2 Transcript intron_variant - - - - - - rs759672 3:185928970 G CCDS43181.1 CCDS43181.1 Transcript intron_variant - - - - - - rs759672 3:185928970 G 1608 NM_001080744.1 Transcript intron_variant - - - - - - rs759672 3:185928970 G CCDS3274.1 CCDS3274.1 Transcript intron_variant - - - - - - rs759672 3:185928970 G CCDS43182.1 CCDS43182.1 Transcript intron_variant - - - - - - rs4686422 3:186062832 T 1608 NM_001080745.1 Transcript intron_variant - - - - - - rs4686422 3:186062832 T 1608 NM_001346.2 Transcript intron_variant - - - - - - rs4686422 3:186062832 T 1608 NM_001080744.1 Transcript intron_variant - - - - - - rs4686422 3:186062832 T ENSESTG00000025487 ENSESTT00000064330 Transcript intron_variant - - - - - - rs850301 3:186982182 G - ENSR00001382044 RegulatoryFeature regulatory_region_variant - - - - - - rs850301 3:186982182 G CCDS33908.1 CCDS33908.1 Transcript intron_variant - - - - - - rs850301 3:186982182 G ENSESTG00000019054 ENSESTT00000048132 Transcript intron_variant - - - - - - rs850301 3:186982182 G 5648 NM_139125.3 Transcript intron_variant - - - - - - rs850301 3:186982182 G CCDS33909.1 CCDS33909.1 Transcript intron_variant - - - - - - rs850301 3:186982182 G ENSESTG00000019054 ENSESTT00000048088 Transcript intron_variant - - - - - - rs850301 3:186982182 G ENSESTG00000019054 ENSESTT00000048109 Transcript intron_variant - - - - - - rs850301 3:186982182 G 5648 NR_033519.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs850301 3:186982182 G 5648 NM_001879.5 Transcript intron_variant - - - - - - rs850301 3:186982182 G CCDS33907.1 CCDS33907.1 Transcript intron_variant - - - - - - rs850301 3:186982182 G ENSESTG00000019054 ENSESTT00000048077 Transcript intron_variant - - - - - - rs850301 3:186982182 G 5648 NM_001031849.2 Transcript intron_variant - - - - - - rs6444219 3:187081895 T ENSESTG00000026387 ENSESTT00000066494 Transcript upstream_gene_variant - - - - - - DISTANCE=4281 rs6444219 3:187081895 T CCDS33910.1 CCDS33910.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4335 rs6444219 3:187081895 T 64108 NM_022147.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4273 rs1880097 3:187364436 T - - - intergenic_variant - - - - - - rs6806296 3:188032235 T 4026 NM_001167671.1 Transcript intron_variant - - - - - - rs6806296 3:188032235 T ENSESTG00000026594 ENSESTT00000067053 Transcript intron_variant - - - - - - rs6806296 3:188032235 T ENSESTG00000026594 ENSESTT00000066984 Transcript intron_variant - - - - - - rs6806296 3:188032235 T ENSESTG00000026594 ENSESTT00000066969 Transcript intron_variant - - - - - - rs6806296 3:188032235 T ENSESTG00000026594 ENSESTT00000067070 Transcript intron_variant - - - - - - rs6806296 3:188032235 T ENSESTG00000026594 ENSESTT00000067082 Transcript intron_variant - - - - - - rs6806296 3:188032235 T ENSESTG00000026594 ENSESTT00000067029 Transcript intron_variant - - - - - - rs6806296 3:188032235 T 4026 NM_001167672.1 Transcript intron_variant - - - - - - rs6806296 3:188032235 T ENSESTG00000026594 ENSESTT00000067011 Transcript intron_variant - - - - - - rs6806296 3:188032235 T 4026 NM_005578.3 Transcript intron_variant - - - - - - rs7651820 3:188067762 T - ENSR00001382277 RegulatoryFeature regulatory_region_variant - - - - - - rs7651820 3:188067762 T 4026 NM_001167671.1 Transcript intron_variant - - - - - - rs7651820 3:188067762 T ENSESTG00000026594 ENSESTT00000067053 Transcript intron_variant - - - - - - rs7651820 3:188067762 T ENSESTG00000026594 ENSESTT00000066984 Transcript intron_variant - - - - - - rs7651820 3:188067762 T ENSESTG00000026594 ENSESTT00000066969 Transcript intron_variant - - - - - - rs7651820 3:188067762 T ENSESTG00000026594 ENSESTT00000067070 Transcript intron_variant - - - - - - rs7651820 3:188067762 T ENSESTG00000026594 ENSESTT00000067082 Transcript intron_variant - - - - - - rs7651820 3:188067762 T ENSESTG00000026594 ENSESTT00000067029 Transcript intron_variant - - - - - - rs7651820 3:188067762 T 4026 NM_001167672.1 Transcript intron_variant - - - - - - rs7651820 3:188067762 T ENSESTG00000026594 ENSESTT00000067011 Transcript intron_variant - - - - - - rs7651820 3:188067762 T 4026 NM_005578.3 Transcript intron_variant - - - - - - rs12107627 3:188114575 G 4026 NM_001167671.1 Transcript intron_variant - - - - - - rs12107627 3:188114575 G ENSESTG00000026594 ENSESTT00000067053 Transcript intron_variant - - - - - - rs12107627 3:188114575 G ENSESTG00000026594 ENSESTT00000066984 Transcript intron_variant - - - - - - rs12107627 3:188114575 G ENSESTG00000026594 ENSESTT00000066969 Transcript intron_variant - - - - - - rs12107627 3:188114575 G ENSESTG00000026594 ENSESTT00000067070 Transcript intron_variant - - - - - - rs12107627 3:188114575 G ENSESTG00000026594 ENSESTT00000067082 Transcript intron_variant - - - - - - rs12107627 3:188114575 G ENSESTG00000026594 ENSESTT00000067029 Transcript intron_variant - - - - - - rs12107627 3:188114575 G 4026 NM_001167672.1 Transcript intron_variant - - - - - - rs12107627 3:188114575 G ENSESTG00000026594 ENSESTT00000067011 Transcript intron_variant - - - - - - rs12107627 3:188114575 G 4026 NM_005578.3 Transcript intron_variant - - - - - - rs2162262 3:188190804 C 4026 NM_001167671.1 Transcript intron_variant - - - - - - rs2162262 3:188190804 C ENSESTG00000017099 ENSESTT00000042991 Transcript intron_variant - - - - - - rs2162262 3:188190804 C ENSESTG00000026594 ENSESTT00000067053 Transcript intron_variant - - - - - - rs2162262 3:188190804 C ENSESTG00000026594 ENSESTT00000066969 Transcript intron_variant - - - - - - rs2162262 3:188190804 C ENSESTG00000026594 ENSESTT00000067029 Transcript intron_variant - - - - - - rs2162262 3:188190804 C 4026 NM_001167672.1 Transcript intron_variant - - - - - - rs2162262 3:188190804 C CCDS3291.1 CCDS3291.1 Transcript intron_variant - - - - - - rs2162262 3:188190804 C 4026 NM_005578.3 Transcript intron_variant - - - - - - rs7641076 3:188294616 T 4026 NM_001167671.1 Transcript intron_variant - - - - - - rs7641076 3:188294616 T ENSESTG00000017099 ENSESTT00000042991 Transcript intron_variant - - - - - - rs7641076 3:188294616 T ENSESTG00000026594 ENSESTT00000067053 Transcript intron_variant - - - - - - rs7641076 3:188294616 T CCDS3291.1 CCDS3291.1 Transcript intron_variant - - - - - - rs7641076 3:188294616 T 4026 NM_001167672.1 Transcript intron_variant - - - - - - rs7641076 3:188294616 T 4026 NM_005578.3 Transcript intron_variant - - - - - - rs1266688 3:188968243 A ENSESTG00000017181 ENSESTT00000043196 Transcript intron_variant - - - - - - rs1266688 3:188968243 A 285386 NM_198485.3 Transcript intron_variant - - - - - - rs1266688 3:188968243 A CCDS3292.1 CCDS3292.1 Transcript intron_variant - - - - - - rs1266688 3:188968243 A ENSESTG00000017181 ENSESTT00000043155 Transcript intron_variant - - - - - - rs260590 3:189097434 C ENSESTG00000017205 ENSESTT00000043209 Transcript intron_variant - - - - - - rs260564 3:189120604 A ENSESTG00000017205 ENSESTT00000043209 Transcript intron_variant - - - - - - rs1152853 3:189121772 A ENSESTG00000017205 ENSESTT00000043209 Transcript intron_variant - - - - - - rs260582 3:189136700 G ENSESTG00000017205 ENSESTT00000043209 Transcript intron_variant - - - - - - rs3856773 3:189280027 G - - - intergenic_variant - - - - - - rs4476481 3:189470938 T CCDS46976.1 CCDS46976.1 Transcript intron_variant - - - - - - rs4476481 3:189470938 T 8626 NM_003722.4 Transcript intron_variant - - - - - - rs4476481 3:189470938 T 8626 NM_001114978.1 Transcript intron_variant - - - - - - rs4476481 3:189470938 T CCDS46977.1 CCDS46977.1 Transcript intron_variant - - - - - - rs4476481 3:189470938 T 8626 NM_001114979.1 Transcript intron_variant - - - - - - rs4476481 3:189470938 T CCDS3293.1 CCDS3293.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A CCDS46976.1 CCDS46976.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A 8626 NM_001114980.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A 8626 NM_003722.4 Transcript intron_variant - - - - - - rs1399772 3:189525713 A 8626 NM_001114978.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A ENSESTG00000010479 ENSESTT00000026256 Transcript intron_variant - - - - - - rs1399772 3:189525713 A CCDS46979.1 CCDS46979.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A CCDS46980.1 CCDS46980.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A CCDS3293.1 CCDS3293.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A CCDS46978.1 CCDS46978.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A 8626 NM_001114981.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A 8626 NM_001114982.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A CCDS46977.1 CCDS46977.1 Transcript intron_variant - - - - - - rs1399772 3:189525713 A ENSESTG00000010479 ENSESTT00000026253 Transcript intron_variant - - - - - - rs1399772 3:189525713 A ENSESTG00000010479 ENSESTT00000026251 Transcript intron_variant - - - - - - rs1399772 3:189525713 A 8626 NM_001114979.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A CCDS46976.1 CCDS46976.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A 8626 NM_001114980.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A 8626 NM_003722.4 Transcript intron_variant - - - - - - rs9859681 3:189539341 A 8626 NM_001114978.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A ENSESTG00000010479 ENSESTT00000026256 Transcript intron_variant - - - - - - rs9859681 3:189539341 A CCDS46979.1 CCDS46979.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A CCDS46980.1 CCDS46980.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A CCDS3293.1 CCDS3293.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A CCDS46978.1 CCDS46978.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A 8626 NM_001114981.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A 8626 NM_001114982.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A CCDS46977.1 CCDS46977.1 Transcript intron_variant - - - - - - rs9859681 3:189539341 A ENSESTG00000010479 ENSESTT00000026253 Transcript intron_variant - - - - - - rs9859681 3:189539341 A ENSESTG00000010479 ENSESTT00000026251 Transcript intron_variant - - - - - - rs9859681 3:189539341 A 8626 NM_001114979.1 Transcript intron_variant - - - - - - rs1515486 3:189615174 G CCDS46976.1 CCDS46976.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3164 rs1515486 3:189615174 G 8626 NM_001114980.1 Transcript downstream_gene_variant - - - - - - DISTANCE=106 rs1515486 3:189615174 G 8626 NM_003722.4 Transcript downstream_gene_variant - - - - - - DISTANCE=106 rs1515486 3:189615174 G 8626 NM_001114978.1 Transcript downstream_gene_variant - - - - - - DISTANCE=106 rs1515486 3:189615174 G CCDS46979.1 CCDS46979.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3164 rs1515486 3:189615174 G CCDS3293.1 CCDS3293.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2883 rs1515486 3:189615174 G CCDS46978.1 CCDS46978.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2883 rs1515486 3:189615174 G 8626 NM_001114981.1 Transcript downstream_gene_variant - - - - - - DISTANCE=106 rs1515486 3:189615174 G ENSESTG00000010479 ENSESTT00000026253 Transcript downstream_gene_variant - - - - - - DISTANCE=2573 rs1515486 3:189615174 G ENSESTG00000010479 ENSESTT00000026251 Transcript downstream_gene_variant - - - - - - DISTANCE=2573 rs578280 3:189908005 A - - - intergenic_variant - - - - - - rs4516592 3:190085183 C - - - intergenic_variant - - - - - - rs7611715 3:190492801 T - - - intergenic_variant - - - - - - rs1916630 3:191331578 C - - - intergenic_variant - - - - - - rs2701587 3:192351054 C CCDS46983.1 CCDS46983.1 Transcript intron_variant - - - - - - rs2701587 3:192351054 C 2257 NM_004113.5 Transcript intron_variant - - - - - - rs4547643 3:192437165 T ENSESTG00000013953 ENSESTT00000034861 Transcript intron_variant - - - - - - rs4547643 3:192437165 T CCDS46983.1 CCDS46983.1 Transcript intron_variant - - - - - - rs4547643 3:192437165 T 2257 NM_004113.5 Transcript intron_variant - - - - - - rs2221467 3:192492052 G - - - intergenic_variant - - - - - - rs6785066 3:192591970 T 151963 NM_178496.3 Transcript intron_variant - - - - - - rs6785066 3:192591970 T ENSESTG00000013950 ENSESTT00000034855 Transcript intron_variant - - - - - - rs6785066 3:192591970 T CCDS3302.2 CCDS3302.2 Transcript intron_variant - - - - - - rs2054965 3:193781102 C ENSESTG00000023123 ENSESTT00000058379 Transcript intron_variant - - - - - - rs2054965 3:193781102 C ENSESTG00000023123 ENSESTT00000058387 Transcript intron_variant - - - - - - rs806097 3:194332189 G 93109 NM_001166305.1 Transcript intron_variant - - - - - - rs806097 3:194332189 G ENSESTG00000002000 ENSESTT00000005009 Transcript intron_variant - - - - - - rs806097 3:194332189 G ENSESTG00000002000 ENSESTT00000005032 Transcript upstream_gene_variant - - - - - - DISTANCE=482 rs806097 3:194332189 G ENSESTG00000002000 ENSESTT00000005014 Transcript intron_variant - - - - - - rs806097 3:194332189 G 93109 NM_001011655.2 Transcript intron_variant - - - - - - rs806097 3:194332189 G CCDS54698.1 CCDS54698.1 Transcript intron_variant - - - - - - rs806097 3:194332189 G ENSESTG00000002000 ENSESTT00000005025 Transcript intron_variant - - - - - - rs806097 3:194332189 G 93109 NM_001166306.1 Transcript intron_variant - - - - - - rs806097 3:194332189 G CCDS3308.2 CCDS3308.2 Transcript intron_variant - - - - - - rs806097 3:194332189 G ENSESTG00000002000 ENSESTT00000005028 Transcript intron_variant - - - - - - rs806097 3:194332189 G ENSESTG00000002000 ENSESTT00000005007 Transcript intron_variant - - - - - - rs806097 3:194332189 G 93109 NM_138399.4 Transcript intron_variant - - - - - - rs806097 3:194332189 G CCDS33921.1 CCDS33921.1 Transcript intron_variant - - - - - - rs806097 3:194332189 G CCDS54699.1 CCDS54699.1 Transcript intron_variant - - - - - - rs486248 3:195738425 G - - - intergenic_variant - - - - - - rs9842616 3:196294104 G ENSESTG00000001359 ENSESTT00000003211 Transcript upstream_gene_variant - - - - - - DISTANCE=748 rs9842616 3:196294104 G 200933 NM_001105573.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1621 rs9842616 3:196294104 G ENSESTG00000001572 ENSESTT00000003726 Transcript intron_variant - - - - - - rs9842616 3:196294104 G 348793 NM_182627.1 Transcript 5_prime_UTR_variant 99 - - - - - rs9842616 3:196294104 G ENSESTG00000001572 ENSESTT00000003720 Transcript 5_prime_UTR_variant 231 - - - - - rs9842616 3:196294104 G ENSESTG00000001359 ENSESTT00000003216 Transcript upstream_gene_variant - - - - - - DISTANCE=1705 rs9842616 3:196294104 G ENSESTG00000001572 ENSESTT00000003730 Transcript missense_variant 108 103 35 E/Q Gaa/Caa - rs9842616 3:196294104 G CCDS46985.1 CCDS46985.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1752 rs7640095 3:196304134 G ENSESTG00000001359 ENSESTT00000003216 Transcript intron_variant - - - - - - rs7640095 3:196304134 G ENSESTG00000001359 ENSESTT00000003211 Transcript intron_variant - - - - - - rs7640095 3:196304134 G 200933 NM_001105573.1 Transcript intron_variant - - - - - - rs7640095 3:196304134 G CCDS46985.1 CCDS46985.1 Transcript intron_variant - - - - - - rs9843906 3:196526779 C CCDS3321.1 CCDS3321.1 Transcript intron_variant - - - - - - rs9843906 3:196526779 C 5062 NM_002577.4 Transcript intron_variant - - - - - - rs9843906 3:196526779 C ENSESTG00000001400 ENSESTT00000003355 Transcript intron_variant - - - - - - rs9833707 3:196620237 C CCDS3322.1 CCDS3322.1 Transcript intron_variant - - - - - - rs9833707 3:196620237 C 205564 NM_152699.4 Transcript intron_variant - - - - - - rs4857600 3:197202552 G - - - intergenic_variant - - - - - - rs2780407 4:53498 C - ENSR00001234211 RegulatoryFeature regulatory_region_variant - - - - - - rs2780407 4:53498 C 152687 NM_182524.2 Transcript intron_variant - - - - - - rs2780407 4:53498 C ENSESTG00000034840 ENSESTT00000088070 Transcript intron_variant - - - - - - rs2780407 4:53498 C ENSESTG00000034474 ENSESTT00000087201 Transcript intron_variant - - - - - - rs2780407 4:53498 C ENSESTG00000034474 ENSESTT00000087214 Transcript intron_variant - - - - - - rs6599372 4:76739 A 152687 NM_182524.2 Transcript intron_variant - - - - - - rs6599372 4:76739 A ENSESTG00000034474 ENSESTT00000087201 Transcript intron_variant - - - - - - rs6599372 4:76739 A ENSESTG00000034474 ENSESTT00000087214 Transcript intron_variant - - - - - - rs6599286 4:123189 T ENSESTG00000034485 ENSESTT00000087230 Transcript upstream_gene_variant - - - - - - DISTANCE=1205 rs6599286 4:123189 T ENSESTG00000034474 ENSESTT00000087201 Transcript intron_variant - - - - - - rs6599286 4:123189 T ENSESTG00000034485 ENSESTT00000087228 Transcript upstream_gene_variant - - - - - - DISTANCE=1195 rs6599286 4:123189 T 255403 NM_001039127.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1231 rs7669481 4:405134 T - - - intergenic_variant - - - - - - rs2352938 4:461040 T ENSESTG00000034833 ENSESTT00000088045 Transcript intron_variant - - - - - - rs2352938 4:461040 T 79963 NR_002451.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs2352938 4:461040 T 170960 NM_133474.2 Transcript intron_variant - - - - - - rs2352938 4:461040 T ENSESTG00000034833 ENSESTT00000088046 Transcript intron_variant - - - - - - rs2352938 4:461040 T CCDS46991.1 CCDS46991.1 Transcript intron_variant - - - - - - rs2352938 4:461040 T ENSESTG00000034833 ENSESTT00000088056 Transcript intron_variant - - - - - - rs4690287 4:655702 G CCDS33932.1 CCDS33932.1 Transcript intron_variant - - - - - - rs4690287 4:655702 G ENSESTG00000034572 ENSESTT00000087458 Transcript upstream_gene_variant - - - - - - DISTANCE=1888 rs4690287 4:655702 G CCDS46993.1 CCDS46993.1 Transcript intron_variant - - - - - - rs4690287 4:655702 G 5158 NM_000283.3 Transcript intron_variant - - - - - - rs4690287 4:655702 G ENSESTG00000034552 ENSESTT00000087431 Transcript intron_variant - - - - - - rs4690287 4:655702 G 5158 NM_001145291.1 Transcript intron_variant - - - - - - rs4690287 4:655702 G 5158 NM_001145292.1 Transcript intron_variant - - - - - - rs4690287 4:655702 G CCDS54703.1 CCDS54703.1 Transcript intron_variant - - - - - - rs4690287 4:655702 G ENSESTG00000034572 ENSESTT00000087455 Transcript upstream_gene_variant - - - - - - DISTANCE=1859 rs798736 4:1678474 G - ENSR00001234660 RegulatoryFeature regulatory_region_variant - - - - - - rs798736 4:1678474 G ENSESTG00000023615 ENSESTT00000059559 Transcript intron_variant - - - - - - rs798736 4:1678474 G ENSESTG00000023615 ENSESTT00000059572 Transcript intron_variant - - - - - - rs798736 4:1678474 G 152877 NM_001174070.1 Transcript intron_variant - - - - - - rs798736 4:1678474 G 152877 NM_001013622.3 Transcript intron_variant - - - - - - rs1794362 4:2183376 A 353497 NM_181808.2 Transcript intron_variant - - - - - - rs1794362 4:2183376 A CCDS3360.1 CCDS3360.1 Transcript intron_variant - - - - - - rs1794362 4:2183376 A ENSESTG00000017839 ENSESTT00000044940 Transcript intron_variant - - - - - - rs1794362 4:2183376 A ENSESTG00000017850 ENSESTT00000044964 Transcript intron_variant - - - - - - rs3108492 4:2485941 G ENSESTG00000016748 ENSESTT00000042163 Transcript intron_variant - - - - - - rs3108492 4:2485941 G ENSESTG00000016748 ENSESTT00000042247 Transcript intron_variant - - - - - - rs3108492 4:2485941 G ENSESTG00000017716 ENSESTT00000044619 Transcript intron_variant - - - - - - rs3108492 4:2485941 G 6047 NM_001185010.2 Transcript intron_variant - - - - - - rs3108492 4:2485941 G ENSESTG00000016748 ENSESTT00000042232 Transcript intron_variant - - - - - - rs3108492 4:2485941 G ENSESTG00000016748 ENSESTT00000042172 Transcript intron_variant - - - - - - rs3108492 4:2485941 G ENSESTG00000016748 ENSESTT00000042177 Transcript intron_variant - - - - - - rs3108492 4:2485941 G ENSESTG00000016748 ENSESTT00000042054 Transcript intron_variant - - - - - - rs3108492 4:2485941 G 6047 NM_002938.4 Transcript intron_variant - - - - - - rs3108492 4:2485941 G ENSESTG00000016748 ENSESTT00000042217 Transcript intron_variant - - - - - - rs3108492 4:2485941 G 6047 NM_001185009.2 Transcript intron_variant - - - - - - rs3108492 4:2485941 G ENSESTG00000016748 ENSESTT00000042076 Transcript intron_variant - - - - - - rs1263310 4:3023178 C CCDS33946.1 CCDS33946.1 Transcript intron_variant - - - - - - rs1263310 4:3023178 C ENSESTG00000007056 ENSESTT00000017889 Transcript downstream_gene_variant - - - - - - DISTANCE=1674 rs1263310 4:3023178 C ENSESTG00000007078 ENSESTT00000017902 Transcript upstream_gene_variant - - - - - - DISTANCE=961 rs1263310 4:3023178 C CCDS33947.1 CCDS33947.1 Transcript intron_variant - - - - - - rs1263310 4:3023178 C 2868 NM_001004056.1 Transcript intron_variant - - - - - - rs1263310 4:3023178 C 2868 NM_182982.2 Transcript intron_variant - - - - - - rs1263310 4:3023178 C 2868 NM_001004057.1 Transcript intron_variant - - - - - - rs1263310 4:3023178 C CCDS47002.1 CCDS47002.1 Transcript intron_variant - - - - - - rs1263310 4:3023178 C ENSESTG00000007056 ENSESTT00000017886 Transcript downstream_gene_variant - - - - - - DISTANCE=1674 rs4325970 4:3475252 C 285489 NM_001164673.1 Transcript synonymous_variant 290 220 74 L Ttg/Ctg - rs4325970 4:3475252 C ENSESTG00000007337 ENSESTT00000018472 Transcript upstream_gene_variant - - - - - - DISTANCE=1420 rs4325970 4:3475252 C 285489 NM_173660.4 Transcript synonymous_variant 290 220 74 L Ttg/Ctg - rs4325970 4:3475252 C ENSESTG00000007318 ENSESTT00000018462 Transcript intron_variant - - - - - - rs4325970 4:3475252 C CCDS54717.1 CCDS54717.1 Transcript synonymous_variant 220 220 74 L Ttg/Ctg - rs4325970 4:3475252 C CCDS3370.2 CCDS3370.2 Transcript synonymous_variant 220 220 74 L Ttg/Ctg - rs4325970 4:3475252 C ENSESTG00000007318 ENSESTT00000018454 Transcript synonymous_variant 290 220 74 L Ttg/Ctg - rs2699405 4:3504275 G 4043 NM_002337.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1049 rs2748765 4:3722027 T - - - intergenic_variant - - - - - - rs6605355 4:3779678 C - - - intergenic_variant - - - - - - rs7376390 4:4276132 C CCDS3374.1 CCDS3374.1 Transcript missense_variant 794 794 265 H/R cAc/cGc - PolyPhen=benign;SIFT=tolerated rs7376390 4:4276132 C ENSESTG00000030796 ENSESTT00000077689 Transcript missense_variant 1027 794 265 H/R cAc/cGc - PolyPhen=benign;SIFT=tolerated rs7376390 4:4276132 C 55646 NM_001145725.1 Transcript missense_variant 937 794 265 H/R cAc/cGc - PolyPhen=benign;SIFT=tolerated rs7376390 4:4276132 C 55646 NM_017816.2 Transcript missense_variant 1035 794 265 H/R cAc/cGc - PolyPhen=benign;SIFT=tolerated rs2980182 4:4319564 C CCDS3375.1 CCDS3375.1 Transcript intron_variant - - - - - - rs2980182 4:4319564 C 166793 NM_145291.3 Transcript intron_variant - - - - - - rs2920189 4:4329343 C - ENSR00001235381 RegulatoryFeature regulatory_region_variant - - - - - - rs2920189 4:4329343 C - - - intergenic_variant - - - - - - rs4386546 4:4848958 C - - - intergenic_variant - - - - - - rs6838134 4:4964311 G - - - intergenic_variant - - - - - - rs6820421 4:5050467 T ENSESTG00000005663 ENSESTT00000014353 Transcript upstream_gene_variant - - - - - - DISTANCE=2471 rs6820421 4:5050467 T 55351 NM_018401.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3060 rs6820421 4:5050467 T ENSESTG00000005663 ENSESTT00000014359 Transcript upstream_gene_variant - - - - - - DISTANCE=2471 rs6820421 4:5050467 T ENSESTG00000005663 ENSESTT00000014368 Transcript upstream_gene_variant - - - - - - DISTANCE=2471 rs6820421 4:5050467 T CCDS3380.1 CCDS3380.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3124 rs6820421 4:5050467 T ENSESTG00000005663 ENSESTT00000014362 Transcript upstream_gene_variant - - - - - - DISTANCE=2471 rs1597017 4:5090493 A ENSESTG00000005663 ENSESTT00000014353 Transcript intron_variant - - - - - - rs1597017 4:5090493 A 55351 NM_018401.1 Transcript intron_variant - - - - - - rs1597017 4:5090493 A ENSESTG00000005663 ENSESTT00000014359 Transcript intron_variant - - - - - - rs1597017 4:5090493 A ENSESTG00000005663 ENSESTT00000014368 Transcript intron_variant - - - - - - rs1597017 4:5090493 A CCDS3380.1 CCDS3380.1 Transcript intron_variant - - - - - - rs1597017 4:5090493 A ENSESTG00000005663 ENSESTT00000014362 Transcript intron_variant - - - - - - rs4689303 4:5795616 A ENSESTG00000005690 ENSESTT00000014429 Transcript upstream_gene_variant - - - - - - DISTANCE=4733 rs4689303 4:5795616 A ENSESTG00000005690 ENSESTT00000014425 Transcript intron_variant - - - - - - rs4689303 4:5795616 A CCDS3383.1 CCDS3383.1 Transcript intron_variant - - - - - - rs4689303 4:5795616 A 2121 NM_153717.2 Transcript intron_variant - - - - - - rs4346592 4:6051288 G 152789 NM_144720.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4194 rs4346592 4:6051288 G CCDS3385.1 CCDS3385.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4414 rs4346592 4:6051288 G 152789 NM_001099433.1 Transcript intron_variant - - - - - - rs4346592 4:6051288 G CCDS47005.1 CCDS47005.1 Transcript intron_variant - - - - - - rs4234734 4:6333130 C - ENSR00001235724 RegulatoryFeature regulatory_region_variant - - - - - - rs4234734 4:6333130 C CCDS56305.1 CCDS56305.1 Transcript intron_variant - - - - - - rs4234734 4:6333130 C CCDS56304.1 CCDS56304.1 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000059004 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000058985 Transcript intron_variant - - - - - - rs4234734 4:6333130 C CCDS3388.1 CCDS3388.1 Transcript intron_variant - - - - - - rs4234734 4:6333130 C 5522 NM_181876.2 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000059073 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000059021 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000058917 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000059037 Transcript intron_variant - - - - - - rs4234734 4:6333130 C 5522 NM_001206995.1 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000059071 Transcript intron_variant - - - - - - rs4234734 4:6333130 C 5522 NM_001206996.1 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000058994 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000059019 Transcript intron_variant - - - - - - rs4234734 4:6333130 C 5522 NM_001206994.1 Transcript intron_variant - - - - - - rs4234734 4:6333130 C ENSESTG00000023307 ENSESTT00000059041 Transcript intron_variant - - - - - - rs11931570 4:6678854 G - ENSR00001235806 RegulatoryFeature regulatory_region_variant - - - - - - rs11931570 4:6678854 G ENSESTG00000023092 ENSESTT00000058299 Transcript downstream_gene_variant - - - - - - DISTANCE=1081 rs11931570 4:6678854 G 93622 NR_015433.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1080 rs11734898 4:6698667 C 6286 NM_005980.2 Transcript synonymous_variant 280 186 62 D gaT/gaC - rs11734898 4:6698667 C ENSESTG00000023108 ENSESTT00000058338 Transcript synonymous_variant 252 186 62 D gaT/gaC - rs11734898 4:6698667 C CCDS3391.1 CCDS3391.1 Transcript synonymous_variant 186 186 62 D gaT/gaC - rs4555719 4:6725300 C - - - intergenic_variant - - - - - - rs7689127 4:6989741 G - ENSR00001235918 RegulatoryFeature regulatory_region_variant - - - - - - rs7689127 4:6989741 G ENSESTG00000034565 ENSESTT00000087448 Transcript intron_variant - - - - - - rs7689127 4:6989741 G ENSESTG00000034565 ENSESTT00000087439 Transcript intron_variant - - - - - - rs7689127 4:6989741 G CCDS3394.2 CCDS3394.2 Transcript intron_variant - - - - - - rs7689127 4:6989741 G ENSESTG00000023219 ENSESTT00000058647 Transcript intron_variant - - - - - - rs7689127 4:6989741 G 57533 NM_001113363.1 Transcript intron_variant - - - - - - rs7689127 4:6989741 G ENSESTG00000023219 ENSESTT00000058673 Transcript intron_variant - - - - - - rs7689127 4:6989741 G CCDS47006.1 CCDS47006.1 Transcript intron_variant - - - - - - rs7689127 4:6989741 G ENSESTG00000034565 ENSESTT00000087450 Transcript intron_variant - - - - - - rs7689127 4:6989741 G 57533 NM_001113361.1 Transcript intron_variant - - - - - - rs7689127 4:6989741 G 57533 NM_020773.2 Transcript intron_variant - - - - - - rs3913448 4:7285848 G 57537 NM_020777.2 Transcript intron_variant - - - - - - rs3913448 4:7285848 G CCDS47008.1 CCDS47008.1 Transcript intron_variant - - - - - - rs4234817 4:7489471 T ENSESTG00000034594 ENSESTT00000087501 Transcript intron_variant - - - - - - rs4234817 4:7489471 T 57537 NM_020777.2 Transcript intron_variant - - - - - - rs4234817 4:7489471 T CCDS47008.1 CCDS47008.1 Transcript intron_variant - - - - - - rs6838686 4:7917963 T 60312 NM_001134647.1 Transcript intron_variant - - - - - - rs6838686 4:7917963 T 60312 NM_198595.2 Transcript intron_variant - - - - - - rs6838686 4:7917963 T ENSESTG00000034651 ENSESTT00000087615 Transcript intron_variant - - - - - - rs1568195 4:8113279 C ENSESTG00000031531 ENSESTT00000079554 Transcript intron_variant - - - - - - rs1568195 4:8113279 C CCDS47013.1 CCDS47013.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C 84448 NM_001130086.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C CCDS47011.1 CCDS47011.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C 84448 NM_001130087.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C CCDS47012.1 CCDS47012.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C CCDS47014.1 CCDS47014.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C 84448 NM_001130084.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C CCDS54719.1 CCDS54719.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C CCDS47016.1 CCDS47016.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C ENSESTG00000031531 ENSESTT00000079560 Transcript intron_variant - - - - - - rs1568195 4:8113279 C 84448 NM_032432.4 Transcript intron_variant - - - - - - rs1568195 4:8113279 C CCDS47015.1 CCDS47015.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C 84448 NM_001130083.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C 84448 NM_001130088.1 Transcript intron_variant - - - - - - rs1568195 4:8113279 C 84448 NM_001130085.1 Transcript intron_variant - - - - - - rs4340781 4:8373032 C - ENSR00001429307 RegulatoryFeature regulatory_region_variant - - - - - - rs4340781 4:8373032 C ENSESTG00000031448 ENSESTT00000079497 Transcript downstream_gene_variant - - - - - - DISTANCE=3670 rs4340781 4:8373032 C ENSESTG00000031448 ENSESTT00000079457 Transcript downstream_gene_variant - - - - - - DISTANCE=3670 rs4340781 4:8373032 C CCDS47017.1 CCDS47017.1 Transcript intron_variant - - - - - - rs4340781 4:8373032 C ENSESTG00000031448 ENSESTT00000079498 Transcript downstream_gene_variant - - - - - - DISTANCE=3825 rs4340781 4:8373032 C ENSESTG00000031448 ENSESTT00000079482 Transcript downstream_gene_variant - - - - - - DISTANCE=3670 rs4340781 4:8373032 C CCDS3401.1 CCDS3401.1 Transcript intron_variant - - - - - - rs4340781 4:8373032 C ENSESTG00000031448 ENSESTT00000079468 Transcript downstream_gene_variant - - - - - - DISTANCE=3825 rs4340781 4:8373032 C 8310 NM_003501.2 Transcript intron_variant - - - - - - rs4340781 4:8373032 C 8310 NM_001101667.1 Transcript intron_variant - - - - - - rs4340781 4:8373032 C ENSESTG00000031448 ENSESTT00000079484 Transcript downstream_gene_variant - - - - - - DISTANCE=3825 rs4696689 4:8397559 A ENSESTG00000031448 ENSESTT00000079497 Transcript intron_variant - - - - - - rs4696689 4:8397559 A ENSESTG00000031448 ENSESTT00000079457 Transcript intron_variant - - - - - - rs4696689 4:8397559 A CCDS47017.1 CCDS47017.1 Transcript intron_variant - - - - - - rs4696689 4:8397559 A ENSESTG00000031448 ENSESTT00000079498 Transcript intron_variant - - - - - - rs4696689 4:8397559 A ENSESTG00000031448 ENSESTT00000079482 Transcript intron_variant - - - - - - rs4696689 4:8397559 A CCDS3401.1 CCDS3401.1 Transcript intron_variant - - - - - - rs4696689 4:8397559 A ENSESTG00000031448 ENSESTT00000079468 Transcript intron_variant - - - - - - rs4696689 4:8397559 A 8310 NM_003501.2 Transcript intron_variant - - - - - - rs4696689 4:8397559 A 8310 NM_001101667.1 Transcript intron_variant - - - - - - rs4696689 4:8397559 A ENSESTG00000031448 ENSESTT00000079484 Transcript intron_variant - - - - - - rs2631759 4:8496689 C ENSESTG00000031334 ENSESTT00000079018 Transcript intron_variant - - - - - - rs138845175 4:8740935 C - - - intergenic_variant - - - - - - rs150516241 4:8773471 A - - - intergenic_variant - - - - - - rs3976630 4:9130383 G - - - intergenic_variant - - - - - - rs1842496 4:9575642 C - - - intergenic_variant - - - - - - rs4697897 4:9850184 T ENSESTG00000001317 ENSESTT00000003113 Transcript intron_variant - - - - - - rs4697897 4:9850184 T 56606 NM_001001290.1 Transcript intron_variant - - - - - - rs4697897 4:9850184 T 56606 NM_020041.2 Transcript intron_variant - - - - - - rs4697897 4:9850184 T CCDS3407.1 CCDS3407.1 Transcript intron_variant - - - - - - rs4697897 4:9850184 T CCDS3406.1 CCDS3406.1 Transcript intron_variant - - - - - - rs6835326 4:10021839 A ENSESTG00000000466 ENSESTT00000001155 Transcript intron_variant - - - - - - rs6835326 4:10021839 A 56606 NM_001001290.1 Transcript intron_variant - - - - - - rs6835326 4:10021839 A 56606 NM_020041.2 Transcript intron_variant - - - - - - rs6835326 4:10021839 A ENSESTG00000000466 ENSESTT00000001163 Transcript intron_variant - - - - - - rs6835326 4:10021839 A ENSESTG00000001311 ENSESTT00000003092 Transcript intron_variant - - - - - - rs6835326 4:10021839 A ENSESTG00000000466 ENSESTT00000001166 Transcript intron_variant - - - - - - rs6835326 4:10021839 A CCDS3407.1 CCDS3407.1 Transcript intron_variant - - - - - - rs6835326 4:10021839 A CCDS3406.1 CCDS3406.1 Transcript intron_variant - - - - - - rs4697919 4:10105917 C ENSESTG00000000432 ENSESTT00000001109 Transcript intron_variant - - - - - - rs4697919 4:10105917 C CCDS54739.1 CCDS54739.1 Transcript intron_variant - - - - - - rs4697919 4:10105917 C ENSESTG00000000432 ENSESTT00000001099 Transcript intron_variant - - - - - - rs4697919 4:10105917 C 9948 NM_005112.4 Transcript intron_variant - - - - - - rs4697919 4:10105917 C CCDS54740.1 CCDS54740.1 Transcript intron_variant - - - - - - rs4697919 4:10105917 C ENSESTG00000000432 ENSESTT00000001138 Transcript intron_variant - - - - - - rs4697919 4:10105917 C ENSESTG00000000432 ENSESTT00000001131 Transcript intron_variant - - - - - - rs4697919 4:10105917 C ENSESTG00000000432 ENSESTT00000001144 Transcript intron_variant - - - - - - rs4697919 4:10105917 C 9948 NM_017491.3 Transcript intron_variant - - - - - - rs4697919 4:10105917 C ENSESTG00000000432 ENSESTT00000001142 Transcript intron_variant - - - - - - rs4697919 4:10105917 C ENSESTG00000000432 ENSESTT00000001088 Transcript intron_variant - - - - - - rs13128688 4:10111855 C ENSESTG00000000432 ENSESTT00000001109 Transcript intron_variant - - - - - - rs13128688 4:10111855 C CCDS54739.1 CCDS54739.1 Transcript intron_variant - - - - - - rs13128688 4:10111855 C ENSESTG00000000432 ENSESTT00000001099 Transcript intron_variant - - - - - - rs13128688 4:10111855 C 9948 NM_005112.4 Transcript intron_variant - - - - - - rs13128688 4:10111855 C CCDS54740.1 CCDS54740.1 Transcript intron_variant - - - - - - rs13128688 4:10111855 C ENSESTG00000000432 ENSESTT00000001138 Transcript intron_variant - - - - - - rs13128688 4:10111855 C ENSESTG00000000432 ENSESTT00000001131 Transcript intron_variant - - - - - - rs13128688 4:10111855 C ENSESTG00000000432 ENSESTT00000001144 Transcript intron_variant - - - - - - rs13128688 4:10111855 C 9948 NM_017491.3 Transcript intron_variant - - - - - - rs13128688 4:10111855 C ENSESTG00000000432 ENSESTT00000001142 Transcript intron_variant - - - - - - rs13128688 4:10111855 C ENSESTG00000000432 ENSESTT00000001088 Transcript intron_variant - - - - - - rs6831320 4:10140265 T - - - intergenic_variant - - - - - - rs887736 4:10171123 G - - - intergenic_variant - - - - - - rs6449394 4:10249075 A - - - intergenic_variant - - - - - - rs1964269 4:10337723 G - - - intergenic_variant - - - - - - rs4697754 4:10385473 C - - - intergenic_variant - - - - - - rs6447983 4:10471587 A - - - intergenic_variant - - - - - - rs4697790 4:10841021 C - - - intergenic_variant - - - - - - rs1881199 4:11269377 G - - - intergenic_variant - - - - - - rs7675275 4:11613218 G - - - intergenic_variant - - - - - - rs10016518 4:11620309 A - ENSR00001236812 RegulatoryFeature regulatory_region_variant - - - - - - rs10016518 4:11620309 A - - - intergenic_variant - - - - - - rs1114554 4:11739676 G - - - intergenic_variant - - - - - - rs1032278 4:11836883 C - - - intergenic_variant - - - - - - rs2130218 4:11910643 C - - - intergenic_variant - - - - - - rs6841200 4:12203368 C - - - intergenic_variant - - - - - - rs7682530 4:12236458 G ENSESTG00000029911 ENSESTT00000075212 Transcript intron_variant - - - - - - rs2085168 4:12279631 G - - - intergenic_variant - - - - - - rs2866450 4:12283651 G - - - intergenic_variant - - - - - - rs4470653 4:12290144 G - - - intergenic_variant - - - - - - rs10939467 4:13249946 G - - - intergenic_variant - - - - - - rs6448992 4:13816177 C - - - intergenic_variant - - - - - - rs10939532 4:14126027 C 152742 NR_033931.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10939532 4:14126027 C ENSESTG00000034276 ENSESTT00000086654 Transcript intron_variant - - - - - - rs10939532 4:14126027 C ENSESTG00000034276 ENSESTT00000086651 Transcript intron_variant - - - - - - rs3846399 4:14127444 C - ENSR00001237040 RegulatoryFeature regulatory_region_variant - - - - - - rs3846399 4:14127444 C 152742 NR_033931.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3846399 4:14127444 C ENSESTG00000034276 ENSESTT00000086654 Transcript intron_variant - - - - - - rs3846399 4:14127444 C ENSESTG00000034276 ENSESTT00000086651 Transcript intron_variant - - - - - - rs3846414 4:14151019 C - - - intergenic_variant - - - - - - rs3843436 4:14152972 C - ENSR00001237043 RegulatoryFeature regulatory_region_variant - - - - - - rs3843436 4:14152972 C - - - intergenic_variant - - - - - - rs3096589 4:14182723 G - ENSR00001237052 RegulatoryFeature regulatory_region_variant - - - - - - rs3096589 4:14182723 G - - - intergenic_variant - - - - - - rs3096588 4:14183669 G - - - intergenic_variant - - - - - - rs10032956 4:14821782 T - - - intergenic_variant - - - - - - rs4493527 4:15224826 G - - - intergenic_variant - - - - - - rs6857460 4:15345301 T ENSESTG00000006243 ENSESTT00000015745 Transcript intron_variant - - - - - - rs6857460 4:15345301 T ENSESTG00000006243 ENSESTT00000015752 Transcript intron_variant - - - - - - rs6857460 4:15345301 T CCDS47025.1 CCDS47025.1 Transcript intron_variant - - - - - - rs6857460 4:15345301 T ENSESTG00000006243 ENSESTT00000015736 Transcript intron_variant - - - - - - rs6857460 4:15345301 T 114905 NM_001135170.1 Transcript intron_variant - - - - - - rs2532076 4:15894285 A - - - intergenic_variant - - - - - - rs3857153 4:16071308 C CCDS47029.1 CCDS47029.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C CCDS54746.1 CCDS54746.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C 8842 NM_001145851.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C ENSESTG00000019151 ENSESTT00000048243 Transcript intron_variant - - - - - - rs3857153 4:16071308 C 8842 NM_001145847.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C ENSESTG00000019151 ENSESTT00000048236 Transcript intron_variant - - - - - - rs3857153 4:16071308 C 8842 NM_001145852.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C CCDS54748.1 CCDS54748.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C 8842 NM_001145848.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C 8842 NM_001145849.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C CCDS54747.1 CCDS54747.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C 8842 NM_001145850.1 Transcript intron_variant - - - - - - rs3857153 4:16071308 C 8842 NM_006017.2 Transcript intron_variant - - - - - - rs4431220 4:16224308 G 202020 NR_027696.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3978 rs4431220 4:16224308 G 202018 NM_153365.2 Transcript intron_variant - - - - - - rs4431220 4:16224308 G CCDS47030.1 CCDS47030.1 Transcript intron_variant - - - - - - rs4431220 4:16224308 G 202020 NR_027697.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3978 rs7699474 4:16604655 C ENSESTG00000019068 ENSESTT00000047977 Transcript intron_variant - - - - - - rs7699474 4:16604655 C 9079 NM_001290.3 Transcript intron_variant - - - - - - rs7699474 4:16604655 C ENSESTG00000019068 ENSESTT00000048010 Transcript intron_variant - - - - - - rs7699474 4:16604655 C CCDS47031.1 CCDS47031.1 Transcript intron_variant - - - - - - rs7699474 4:16604655 C 9079 NM_001130834.1 Transcript intron_variant - - - - - - rs7699474 4:16604655 C CCDS3420.1 CCDS3420.1 Transcript intron_variant - - - - - - rs7378240 4:16885146 T ENSESTG00000019068 ENSESTT00000047977 Transcript intron_variant - - - - - - rs7378240 4:16885146 T ENSESTG00000019068 ENSESTT00000047956 Transcript intron_variant - - - - - - rs7378240 4:16885146 T 9079 NM_001290.3 Transcript intron_variant - - - - - - rs7378240 4:16885146 T CCDS47031.1 CCDS47031.1 Transcript intron_variant - - - - - - rs7378240 4:16885146 T 9079 NM_001130834.1 Transcript intron_variant - - - - - - rs7378240 4:16885146 T CCDS3420.1 CCDS3420.1 Transcript intron_variant - - - - - - rs828167 4:17056935 G - - - intergenic_variant - - - - - - rs6815863 4:17102366 C - - - intergenic_variant - - - - - - rs924788 4:18086182 C - - - intergenic_variant - - - - - - rs7669044 4:18150445 A - - - intergenic_variant - - - - - - rs7684762 4:18295750 C - - - intergenic_variant - - - - - - rs7676568 4:18320547 G - ENSR00001237621 RegulatoryFeature regulatory_region_variant - - - - - - rs7676568 4:18320547 G - - - intergenic_variant - - - - - - rs207364 4:19005503 G - - - intergenic_variant - - - - - - rs4440211 4:19427547 G - - - intergenic_variant - - - - - - rs7663384 4:19825378 T - - - intergenic_variant - - - - - - rs6447933 4:19912930 A - - - intergenic_variant - - - - - - rs4393992 4:19964741 A - - - intergenic_variant - - - - - - rs686869 4:20206651 A - - - intergenic_variant - - - - - - rs674697 4:20303767 T CCDS3426.1 CCDS3426.1 Transcript intron_variant - - - - - - rs674697 4:20303767 T 9353 NM_004787.1 Transcript intron_variant - - - - - - rs10022041 4:20654146 A - - - intergenic_variant - - - - - - rs4697181 4:20794258 T CCDS47035.1 CCDS47035.1 Transcript intron_variant - - - - - - rs4697181 4:20794258 T CCDS43216.1 CCDS43216.1 Transcript intron_variant - - - - - - rs4697181 4:20794258 T ENSESTG00000020781 ENSESTT00000052314 Transcript intron_variant - - - - - - rs4697181 4:20794258 T ENSESTG00000020781 ENSESTT00000052295 Transcript intron_variant - - - - - - rs4697181 4:20794258 T 80333 NM_025221.5 Transcript intron_variant - - - - - - rs4697181 4:20794258 T CCDS43217.1 CCDS43217.1 Transcript intron_variant - - - - - - rs4697181 4:20794258 T 80333 NM_147181.3 Transcript intron_variant - - - - - - rs4697181 4:20794258 T CCDS43215.1 CCDS43215.1 Transcript intron_variant - - - - - - rs4697181 4:20794258 T 80333 NM_001035003.1 Transcript intron_variant - - - - - - rs4697181 4:20794258 T CCDS3428.1 CCDS3428.1 Transcript intron_variant - - - - - - rs4697181 4:20794258 T 80333 NM_001035004.1 Transcript intron_variant - - - - - - rs4697181 4:20794258 T ENSESTG00000020781 ENSESTT00000052367 Transcript intron_variant - - - - - - rs4697181 4:20794258 T ENSESTG00000020781 ENSESTT00000052102 Transcript intron_variant - - - - - - rs4697181 4:20794258 T 80333 NM_147182.3 Transcript intron_variant - - - - - - rs4697181 4:20794258 T 80333 NM_147183.3 Transcript intron_variant - - - - - - rs963623 4:20902235 A CCDS43216.1 CCDS43216.1 Transcript intron_variant - - - - - - rs963623 4:20902235 A 80333 NM_025221.5 Transcript intron_variant - - - - - - rs963623 4:20902235 A CCDS43217.1 CCDS43217.1 Transcript intron_variant - - - - - - rs963623 4:20902235 A 80333 NM_147181.3 Transcript intron_variant - - - - - - rs963623 4:20902235 A CCDS43215.1 CCDS43215.1 Transcript intron_variant - - - - - - rs963623 4:20902235 A 80333 NM_001035003.1 Transcript intron_variant - - - - - - rs963623 4:20902235 A 80333 NM_001035004.1 Transcript intron_variant - - - - - - rs963623 4:20902235 A CCDS3428.1 CCDS3428.1 Transcript intron_variant - - - - - - rs963623 4:20902235 A 80333 NM_147182.3 Transcript intron_variant - - - - - - rs963623 4:20902235 A ENSESTG00000020781 ENSESTT00000052102 Transcript intron_variant - - - - - - rs963623 4:20902235 A 80333 NM_147183.3 Transcript intron_variant - - - - - - rs7685814 4:21009881 T CCDS43216.1 CCDS43216.1 Transcript intron_variant - - - - - - rs7685814 4:21009881 T 80333 NM_025221.5 Transcript intron_variant - - - - - - rs7685814 4:21009881 T CCDS43217.1 CCDS43217.1 Transcript intron_variant - - - - - - rs7685814 4:21009881 T 80333 NM_147181.3 Transcript intron_variant - - - - - - rs7685814 4:21009881 T CCDS43215.1 CCDS43215.1 Transcript intron_variant - - - - - - rs7685814 4:21009881 T 80333 NM_001035003.1 Transcript intron_variant - - - - - - rs7685814 4:21009881 T 80333 NM_001035004.1 Transcript intron_variant - - - - - - rs7685814 4:21009881 T CCDS3428.1 CCDS3428.1 Transcript intron_variant - - - - - - rs7685814 4:21009881 T 80333 NM_147182.3 Transcript intron_variant - - - - - - rs7685814 4:21009881 T 80333 NM_147183.3 Transcript intron_variant - - - - - - rs970410 4:21181340 G CCDS43216.1 CCDS43216.1 Transcript intron_variant - - - - - - rs970410 4:21181340 G 80333 NM_025221.5 Transcript intron_variant - - - - - - rs970410 4:21181340 G CCDS43217.1 CCDS43217.1 Transcript intron_variant - - - - - - rs970410 4:21181340 G 80333 NM_147181.3 Transcript intron_variant - - - - - - rs970410 4:21181340 G CCDS43215.1 CCDS43215.1 Transcript intron_variant - - - - - - rs970410 4:21181340 G 80333 NM_001035003.1 Transcript intron_variant - - - - - - rs970410 4:21181340 G 80333 NM_001035004.1 Transcript intron_variant - - - - - - rs970410 4:21181340 G CCDS3428.1 CCDS3428.1 Transcript intron_variant - - - - - - rs970410 4:21181340 G 80333 NM_147182.3 Transcript intron_variant - - - - - - rs970410 4:21181340 G 80333 NM_147183.3 Transcript intron_variant - - - - - - rs10022849 4:21332275 G CCDS43216.1 CCDS43216.1 Transcript intron_variant - - - - - - rs10022849 4:21332275 G 80333 NM_025221.5 Transcript intron_variant - - - - - - rs10022849 4:21332275 G CCDS43217.1 CCDS43217.1 Transcript intron_variant - - - - - - rs10022849 4:21332275 G 80333 NM_147181.3 Transcript intron_variant - - - - - - rs10022849 4:21332275 G CCDS43215.1 CCDS43215.1 Transcript intron_variant - - - - - - rs10022849 4:21332275 G 80333 NM_001035003.1 Transcript intron_variant - - - - - - rs10022849 4:21332275 G 80333 NM_001035004.1 Transcript intron_variant - - - - - - rs10022849 4:21332275 G 80333 NM_147182.3 Transcript intron_variant - - - - - - rs664565 4:21433883 G CCDS43216.1 CCDS43216.1 Transcript intron_variant - - - - - - rs664565 4:21433883 G 80333 NM_025221.5 Transcript intron_variant - - - - - - rs664565 4:21433883 G CCDS43217.1 CCDS43217.1 Transcript intron_variant - - - - - - rs664565 4:21433883 G 80333 NM_147181.3 Transcript intron_variant - - - - - - rs664565 4:21433883 G CCDS43215.1 CCDS43215.1 Transcript intron_variant - - - - - - rs664565 4:21433883 G 80333 NM_001035003.1 Transcript intron_variant - - - - - - rs664565 4:21433883 G 80333 NM_001035004.1 Transcript intron_variant - - - - - - rs664565 4:21433883 G 80333 NM_147182.3 Transcript intron_variant - - - - - - rs368431 4:21515621 T CCDS43216.1 CCDS43216.1 Transcript intron_variant - - - - - - rs368431 4:21515621 T 80333 NM_025221.5 Transcript intron_variant - - - - - - rs368431 4:21515621 T CCDS43217.1 CCDS43217.1 Transcript intron_variant - - - - - - rs368431 4:21515621 T 80333 NM_147181.3 Transcript intron_variant - - - - - - rs368431 4:21515621 T CCDS43215.1 CCDS43215.1 Transcript intron_variant - - - - - - rs368431 4:21515621 T 80333 NM_001035003.1 Transcript intron_variant - - - - - - rs368431 4:21515621 T 80333 NM_001035004.1 Transcript intron_variant - - - - - - rs368431 4:21515621 T 80333 NM_147182.3 Transcript intron_variant - - - - - - rs1040037 4:21856615 C CCDS43215.1 CCDS43215.1 Transcript intron_variant - - - - - - rs1040037 4:21856615 C 80333 NM_147182.3 Transcript intron_variant - - - - - - rs1040037 4:21856615 C ENSESTG00000018350 ENSESTT00000046161 Transcript intron_variant - - - - - - rs1040037 4:21856615 C CCDS43216.1 CCDS43216.1 Transcript intron_variant - - - - - - rs1040037 4:21856615 C 80333 NM_025221.5 Transcript intron_variant - - - - - - rs1040037 4:21856615 C 359822 NR_002813.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1804 rs1040037 4:21856615 C 80333 NM_147181.3 Transcript intron_variant - - - - - - rs6818512 4:21924670 A CCDS43215.1 CCDS43215.1 Transcript intron_variant - - - - - - rs6818512 4:21924670 A 80333 NM_147182.3 Transcript intron_variant - - - - - - rs6818512 4:21924670 A CCDS43216.1 CCDS43216.1 Transcript intron_variant - - - - - - rs6818512 4:21924670 A 80333 NM_025221.5 Transcript intron_variant - - - - - - rs6818512 4:21924670 A 80333 NM_147181.3 Transcript intron_variant - - - - - - rs6448102 4:21950259 G - ENSR00001237905 RegulatoryFeature regulatory_region_variant - - - - - - rs6448102 4:21950259 G CCDS43215.1 CCDS43215.1 Transcript upstream_gene_variant - - - - - - DISTANCE=5 rs6448102 4:21950259 G 80333 NM_147182.3 Transcript 5_prime_UTR_variant 116 - - - - - rs6448102 4:21950259 G CCDS43216.1 CCDS43216.1 Transcript upstream_gene_variant - - - - - - DISTANCE=5 rs6448102 4:21950259 G 80333 NM_025221.5 Transcript 5_prime_UTR_variant 116 - - - - - rs6448102 4:21950259 G 80333 NM_147181.3 Transcript 5_prime_UTR_variant 116 - - - - - rs2009195 4:21951004 A CCDS43215.1 CCDS43215.1 Transcript upstream_gene_variant - - - - - - DISTANCE=750 rs2009195 4:21951004 A 80333 NM_147182.3 Transcript upstream_gene_variant - - - - - - DISTANCE=630 rs2009195 4:21951004 A CCDS43216.1 CCDS43216.1 Transcript upstream_gene_variant - - - - - - DISTANCE=750 rs2009195 4:21951004 A 80333 NM_025221.5 Transcript upstream_gene_variant - - - - - - DISTANCE=630 rs2009195 4:21951004 A 80333 NM_147181.3 Transcript upstream_gene_variant - - - - - - DISTANCE=630 rs6816972 4:21967490 G - - - intergenic_variant - - - - - - rs1828710 4:21974625 T - - - intergenic_variant - - - - - - rs1849543 4:21977056 C - - - intergenic_variant - - - - - - rs990093 4:21981385 A - - - intergenic_variant - - - - - - rs4385047 4:21992534 G - - - intergenic_variant - - - - - - rs1828709 4:22026299 G - - - intergenic_variant - - - - - - rs4346634 4:22042573 C - - - intergenic_variant - - - - - - rs1354000 4:22294791 C - - - intergenic_variant - - - - - - rs6812413 4:22328645 C 100505912 NR_037877.1 Transcript downstream_gene_variant - - - - - - DISTANCE=332 rs4697288 4:22333901 C 100505912 NR_037877.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6831475 4:22336971 C 100505912 NR_037877.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6448149 4:22345338 C - ENSR00001429988 RegulatoryFeature regulatory_region_variant - - - - - - rs6448149 4:22345338 C 100505912 NR_037877.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4049 rs6824928 4:22366288 C - - - intergenic_variant - - - - - - rs7664213 4:22386810 G 166647 NM_145290.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2189 rs7664213 4:22386810 G ENSESTG00000031917 ENSESTT00000080674 Transcript downstream_gene_variant - - - - - - DISTANCE=3478 rs7664213 4:22386810 G CCDS33964.1 CCDS33964.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2518 rs9790456 4:22410138 C 166647 NM_145290.2 Transcript intron_variant - - - - - - rs9790456 4:22410138 C ENSESTG00000031917 ENSESTT00000080674 Transcript intron_variant - - - - - - rs9790456 4:22410138 C CCDS33964.1 CCDS33964.1 Transcript intron_variant - - - - - - rs9999224 4:22418402 T - ENSR00001237928 RegulatoryFeature regulatory_region_variant - - - - - - rs9999224 4:22418402 T 166647 NM_145290.2 Transcript intron_variant - - - - - - rs9999224 4:22418402 T ENSESTG00000031917 ENSESTT00000080674 Transcript intron_variant - - - - - - rs9999224 4:22418402 T CCDS33964.1 CCDS33964.1 Transcript intron_variant - - - - - - rs1392594 4:22427261 C 166647 NM_145290.2 Transcript intron_variant - - - - - - rs1392594 4:22427261 C ENSESTG00000031917 ENSESTT00000080674 Transcript intron_variant - - - - - - rs1392594 4:22427261 C CCDS33964.1 CCDS33964.1 Transcript intron_variant - - - - - - rs7658694 4:22442092 C 166647 NM_145290.2 Transcript intron_variant - - - - - - rs7658694 4:22442092 C ENSESTG00000031893 ENSESTT00000080470 Transcript upstream_gene_variant - - - - - - DISTANCE=2248 rs7658694 4:22442092 C ENSESTG00000031917 ENSESTT00000080674 Transcript intron_variant - - - - - - rs7658694 4:22442092 C CCDS33964.1 CCDS33964.1 Transcript intron_variant - - - - - - rs7658694 4:22442092 C ENSESTG00000031917 ENSESTT00000080701 Transcript downstream_gene_variant - - - - - - DISTANCE=2225 rs4697299 4:22448273 A 166647 NM_145290.2 Transcript intron_variant - - - - - - rs4697299 4:22448273 A ENSESTG00000031893 ENSESTT00000080470 Transcript downstream_gene_variant - - - - - - DISTANCE=1520 rs4697299 4:22448273 A ENSESTG00000031917 ENSESTT00000080674 Transcript intron_variant - - - - - - rs4697299 4:22448273 A CCDS33964.1 CCDS33964.1 Transcript intron_variant - - - - - - rs4697299 4:22448273 A ENSESTG00000031917 ENSESTT00000080701 Transcript intron_variant - - - - - - rs4697311 4:22503484 T - ENSR00001237950 RegulatoryFeature regulatory_region_variant - - - - - - rs4697311 4:22503484 T ENSESTG00000031917 ENSESTT00000080688 Transcript intron_variant - - - - - - rs4697311 4:22503484 T 166647 NM_145290.2 Transcript intron_variant - - - - - - rs4697311 4:22503484 T ENSESTG00000031917 ENSESTT00000080674 Transcript intron_variant - - - - - - rs4697311 4:22503484 T CCDS33964.1 CCDS33964.1 Transcript intron_variant - - - - - - rs10222757 4:22514027 C - ENSR00001237955 RegulatoryFeature regulatory_region_variant - - - - - - rs10222757 4:22514027 C ENSESTG00000031917 ENSESTT00000080688 Transcript intron_variant - - - - - - rs10222757 4:22514027 C 166647 NM_145290.2 Transcript intron_variant - - - - - - rs10222757 4:22514027 C ENSESTG00000031917 ENSESTT00000080674 Transcript intron_variant - - - - - - rs10222757 4:22514027 C CCDS33964.1 CCDS33964.1 Transcript intron_variant - - - - - - rs2010731 4:22533757 G - - - intergenic_variant - - - - - - rs1462993 4:22537979 C - - - intergenic_variant - - - - - - rs1462991 4:22553896 A - - - intergenic_variant - - - - - - rs2323617 4:22564985 G - - - intergenic_variant - - - - - - rs4697321 4:22565808 G - - - intergenic_variant - - - - - - rs2618925 4:22678772 T - - - intergenic_variant - - - - - - rs1503674 4:23073911 G - - - intergenic_variant - - - - - - rs4317190 4:23214349 G - - - intergenic_variant - - - - - - rs216104 4:23499572 T - - - intergenic_variant - - - - - - rs9996366 4:23876355 C 10891 NM_013261.3 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016571 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016545 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016560 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016543 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016534 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016564 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016573 Transcript intron_variant - - - - - - rs9996366 4:23876355 C CCDS3429.1 CCDS3429.1 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016523 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016528 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016540 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016567 Transcript downstream_gene_variant - - - - - - DISTANCE=2964 rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016546 Transcript intron_variant - - - - - - rs9996366 4:23876355 C ENSESTG00000006550 ENSESTT00000016563 Transcript intron_variant - - - - - - rs4697427 4:23935037 G - ENSR00001430108 RegulatoryFeature regulatory_region_variant - - - - - - rs4697427 4:23935037 G - - - intergenic_variant - - - - - - rs582394 4:23992551 A - - - intergenic_variant - - - - - - rs626241 4:24048525 C - - - intergenic_variant - - - - - - rs2324419 4:24194704 T - - - intergenic_variant - - - - - - rs7670798 4:24606030 A - - - intergenic_variant - - - - - - rs4235319 4:24699980 A ENSESTG00000002386 ENSESTT00000005922 Transcript intron_variant - - - - - - rs6820670 4:24720865 G ENSESTG00000002386 ENSESTT00000005922 Transcript intron_variant - - - - - - rs6448301 4:24731376 C ENSESTG00000002386 ENSESTT00000005922 Transcript intron_variant - - - - - - rs6448304 4:24751691 A ENSESTG00000002386 ENSESTT00000005922 Transcript intron_variant - - - - - - rs2667299 4:25331017 G 29063 NM_024936.2 Transcript intron_variant - - - - - - rs2667299 4:25331017 G CCDS43218.1 CCDS43218.1 Transcript intron_variant - - - - - - rs2667299 4:25331017 G ENSESTG00000020068 ENSESTT00000050361 Transcript intron_variant - - - - - - rs315673 4:25368528 A ENSESTG00000020102 ENSESTT00000050480 Transcript downstream_gene_variant - - - - - - DISTANCE=1656 rs315673 4:25368528 A 29063 NM_024936.2 Transcript intron_variant - - - - - - rs315673 4:25368528 A ENSESTG00000020102 ENSESTT00000050502 Transcript intron_variant - - - - - - rs315673 4:25368528 A ENSESTG00000020102 ENSESTT00000050472 Transcript intron_variant - - - - - - rs315673 4:25368528 A CCDS43218.1 CCDS43218.1 Transcript intron_variant - - - - - - rs7690450 4:25452180 A - ENSR00001238331 RegulatoryFeature regulatory_region_variant - - - - - - rs7690450 4:25452180 A - - - intergenic_variant - - - - - - rs6821377 4:25779160 A 23231 NM_015187.3 Transcript intron_variant - - - - - - rs6821377 4:25779160 A CCDS47037.1 CCDS47037.1 Transcript intron_variant - - - - - - rs6821377 4:25779160 A ENSESTG00000020538 ENSESTT00000051583 Transcript intron_variant - - - - - - rs6448433 4:26100908 T - - - intergenic_variant - - - - - - rs1877387 4:26106186 A - - - intergenic_variant - - - - - - rs10470819 4:26510491 G - - - intergenic_variant - - - - - - rs6821361 4:26516672 T - - - intergenic_variant - - - - - - rs6813213 4:26701976 A CCDS3439.1 CCDS3439.1 Transcript intron_variant - - - - - - rs6813213 4:26701976 A ENSESTG00000010676 ENSESTT00000026787 Transcript intron_variant - - - - - - rs6813213 4:26701976 A 55296 NM_018317.2 Transcript intron_variant - - - - - - rs6813213 4:26701976 A ENSESTG00000010676 ENSESTT00000026788 Transcript intron_variant - - - - - - rs6448469 4:26738629 C - ENSR00001238587 RegulatoryFeature regulatory_region_variant - - - - - - rs6448469 4:26738629 C ENSESTG00000010676 ENSESTT00000026800 Transcript intron_variant - - - - - - rs6448469 4:26738629 C CCDS3439.1 CCDS3439.1 Transcript intron_variant - - - - - - rs6448469 4:26738629 C ENSESTG00000010676 ENSESTT00000026787 Transcript intron_variant - - - - - - rs6448469 4:26738629 C 55296 NM_018317.2 Transcript intron_variant - - - - - - rs6448469 4:26738629 C ENSESTG00000010676 ENSESTT00000026788 Transcript intron_variant - - - - - - rs10022338 4:26783701 G - ENSR00001238596 RegulatoryFeature regulatory_region_variant - - - - - - rs10022338 4:26783701 G ENSESTG00000010707 ENSESTT00000026810 Transcript upstream_gene_variant - - - - - - DISTANCE=625 rs10014150 4:28131615 A - - - intergenic_variant - - - - - - rs4586921 4:28475462 G ENSESTG00000004018 ENSESTT00000010160 Transcript upstream_gene_variant - - - - - - DISTANCE=2608 rs4532225 4:28714397 G - - - intergenic_variant - - - - - - rs1402483 4:28991141 T - - - intergenic_variant - - - - - - rs4529119 4:29123696 G - - - intergenic_variant - - - - - - rs10024929 4:29191115 A - - - intergenic_variant - - - - - - rs4235004 4:29306440 C - - - intergenic_variant - - - - - - rs4482721 4:29512093 G - - - intergenic_variant - - - - - - rs1847422 4:29932566 A - - - intergenic_variant - - - - - - rs10939291 4:30088912 G - - - intergenic_variant - - - - - - rs2063414 4:31560114 G - - - intergenic_variant - - - - - - rs1981721 4:31729962 A - - - intergenic_variant - - - - - - rs4412034 4:32028959 C ENSESTG00000015908 ENSESTT00000039897 Transcript intron_variant - - - - - - rs674015 4:32252277 C - - - intergenic_variant - - - - - - rs7671632 4:32715228 T - - - intergenic_variant - - - - - - rs2585988 4:33258955 T - - - intergenic_variant - - - - - - rs2687462 4:33332807 G - - - intergenic_variant - - - - - - rs2337737 4:33360356 T - - - intergenic_variant - - - - - - rs10212924 4:33764703 G - - - intergenic_variant - - - - - - rs7691831 4:33863546 G ENSESTG00000033260 ENSESTT00000084023 Transcript intron_variant - - - - - - rs6531301 4:34210466 T ENSESTG00000033285 ENSESTT00000084076 Transcript intron_variant - - - - - - rs6531301 4:34210466 T ENSESTG00000033285 ENSESTT00000084066 Transcript intron_variant - - - - - - rs4276297 4:34401757 C - - - intergenic_variant - - - - - - rs1218656 4:34464598 C - - - intergenic_variant - - - - - - rs4432762 4:35000039 T - - - intergenic_variant - - - - - - rs3098736 4:35394618 C - - - intergenic_variant - - - - - - rs1501119 4:36258666 G - - - intergenic_variant - - - - - - rs2889229 4:36264667 C - - - intergenic_variant - - - - - - rs1867473 4:36852857 C - - - intergenic_variant - - - - - - rs7698357 4:36854907 C - - - intergenic_variant - - - - - - rs5001826 4:36868174 C - - - intergenic_variant - - - - - - rs2376332 4:36936718 T - - - intergenic_variant - - - - - - rs1035782 4:37057947 G - - - intergenic_variant - - - - - - rs9991440 4:37122064 A ENSESTG00000008629 ENSESTT00000021684 Transcript intron_variant - - - - - - rs1435391 4:37295947 G 57495 NM_001144990.1 Transcript intron_variant - - - - - - rs1435391 4:37295947 G CCDS47040.1 CCDS47040.1 Transcript intron_variant - - - - - - rs1221653 4:37666995 C - ENSR00001239238 RegulatoryFeature regulatory_region_variant - - - - - - rs1221653 4:37666995 C CCDS43221.1 CCDS43221.1 Transcript intron_variant - - - - - - rs1221653 4:37666995 C ENSESTG00000008711 ENSESTT00000021936 Transcript intron_variant - - - - - - rs1221653 4:37666995 C ENSESTG00000008711 ENSESTT00000021929 Transcript intron_variant - - - - - - rs1221653 4:37666995 C ENSESTG00000008711 ENSESTT00000021944 Transcript intron_variant - - - - - - rs1221653 4:37666995 C ENSESTG00000008711 ENSESTT00000021953 Transcript 5_prime_UTR_variant 9 - - - - - rs1221653 4:37666995 C 768211 NM_001085400.1 Transcript intron_variant - - - - - - rs1221653 4:37666995 C 768211 NM_001085399.1 Transcript intron_variant - - - - - - rs4833016 4:38241481 G - - - intergenic_variant - - - - - - rs6819854 4:39563921 C CCDS3456.1 CCDS3456.1 Transcript intron_variant - - - - - - rs6819854 4:39563921 C ENSESTG00000031247 ENSESTT00000078790 Transcript intron_variant - - - - - - rs6819854 4:39563921 C 201895 NM_174921.1 Transcript intron_variant - - - - - - rs6819854 4:39563921 C ENSESTG00000031247 ENSESTT00000078823 Transcript intron_variant - - - - - - rs6819854 4:39563921 C 100885776 NR_047679.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs794030 4:40062314 C ENSESTG00000000867 ENSESTT00000002091 Transcript intron_variant - - - - - - rs794030 4:40062314 C ENSESTG00000000867 ENSESTT00000002094 Transcript intron_variant - - - - - - rs794030 4:40062314 C 344967 NR_027277.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3495 rs794030 4:40062314 C 55728 NM_018177.4 Transcript intron_variant - - - - - - rs2120040 4:43353600 G - - - intergenic_variant - - - - - - rs7668941 4:43781620 A - - - intergenic_variant - - - - - - rs7438438 4:44437623 T ENSESTG00000031177 ENSESTT00000078524 Transcript intron_variant - - - - - - rs7438438 4:44437623 T 386617 NM_198353.2 Transcript intron_variant - - - - - - rs7438438 4:44437623 T CCDS3467.1 CCDS3467.1 Transcript intron_variant - - - - - - rs4353937 4:45017935 T - - - intergenic_variant - - - - - - rs348529 4:45198703 C - - - intergenic_variant - - - - - - rs7680396 4:45728595 A - - - intergenic_variant - - - - - - rs10020723 4:47279430 G ENSESTG00000020520 ENSESTT00000051468 Transcript intron_variant - - - - - - rs10020723 4:47279430 G CCDS3474.1 CCDS3474.1 Transcript intron_variant - - - - - - rs10020723 4:47279430 G ENSESTG00000020520 ENSESTT00000051471 Transcript intron_variant - - - - - - rs10020723 4:47279430 G ENSESTG00000020520 ENSESTT00000051509 Transcript intron_variant - - - - - - rs10020723 4:47279430 G ENSESTG00000020520 ENSESTT00000051526 Transcript intron_variant - - - - - - rs10020723 4:47279430 G 2560 NM_000812.3 Transcript intron_variant - - - - - - rs1396047 4:48044049 T - ENSR00001240567 RegulatoryFeature regulatory_region_variant - - - - - - rs1396047 4:48044049 T 152519 NM_207330.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4965 rs1396047 4:48044049 T ENSESTG00000034526 ENSESTT00000087318 Transcript intron_variant - - - - - - rs1396047 4:48044049 T ENSESTG00000034387 ENSESTT00000086974 Transcript downstream_gene_variant - - - - - - DISTANCE=1859 rs4107078 4:49559796 C - - - intergenic_variant - - - - - - rs900112 4:54193128 A 152579 NM_152540.3 Transcript intron_variant - - - - - - rs900112 4:54193128 A ENSESTG00000024064 ENSESTT00000060882 Transcript intron_variant - - - - - - rs900112 4:54193128 A ENSESTG00000024064 ENSESTT00000060846 Transcript intron_variant - - - - - - rs900112 4:54193128 A CCDS33984.1 CCDS33984.1 Transcript intron_variant - - - - - - rs9884342 4:55762294 C - - - intergenic_variant - - - - - - rs2219470 4:56005935 C - - - intergenic_variant - - - - - - rs10852365 16:13478078 T ENSESTG00000019521 ENSESTT00000049007 Transcript intron_variant - - - - - - rs4277366 16:14597543 C - ENSR00001503847 RegulatoryFeature regulatory_region_variant - - - - - - rs4277366 16:14597543 C ENSESTG00000005058 ENSESTT00000012948 Transcript intron_variant - - - - - - rs4277366 16:14597543 C ENSESTG00000005058 ENSESTT00000012943 Transcript intron_variant - - - - - - rs4277366 16:14597543 C 5073 NM_001134477.2 Transcript intron_variant - - - - - - rs4277366 16:14597543 C ENSESTG00000005058 ENSESTT00000012957 Transcript upstream_gene_variant - - - - - - DISTANCE=1997 rs4277366 16:14597543 C 5073 NM_002582.3 Transcript intron_variant - - - - - - rs4277366 16:14597543 C ENSESTG00000005058 ENSESTT00000012950 Transcript intron_variant - - - - - - rs4277366 16:14597543 C CCDS45420.1 CCDS45420.1 Transcript intron_variant - - - - - - rs4277366 16:14597543 C CCDS45419.1 CCDS45419.1 Transcript intron_variant - - - - - - rs4277366 16:14597543 C 5073 NM_001242992.1 Transcript intron_variant - - - - - - rs4277366 16:14597543 C CCDS58425.1 CCDS58425.1 Transcript intron_variant - - - - - - rs2113324 16:14735008 G CCDS10554.1 CCDS10554.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3196 rs2113324 16:14735008 G ENSESTG00000005014 ENSESTT00000012791 Transcript intron_variant - - - - - - rs2113324 16:14735008 G ENSESTG00000005014 ENSESTT00000012792 Transcript intron_variant - - - - - - rs2113324 16:14735008 G ENSESTG00000005014 ENSESTT00000012796 Transcript intron_variant - - - - - - rs2113324 16:14735008 G 51283 NM_016561.2 Transcript intron_variant - - - - - - rs2113324 16:14735008 G ENSESTG00000005014 ENSESTT00000012783 Transcript intron_variant - - - - - - rs2113324 16:14735008 G ENSESTG00000005014 ENSESTT00000012788 Transcript intron_variant - - - - - - rs2113324 16:14735008 G ENSESTG00000005014 ENSESTT00000012786 Transcript intron_variant - - - - - - rs2113324 16:14735008 G ENSESTG00000005014 ENSESTT00000012800 Transcript intron_variant - - - - - - rs7404069 16:15085744 C 23042 NM_015027.2 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052739 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052868 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052773 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052694 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052838 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052846 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052728 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052759 Transcript intron_variant - - - - - - rs7404069 16:15085744 C CCDS32393.1 CCDS32393.1 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052711 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052664 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052853 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052723 Transcript intron_variant - - - - - - rs7404069 16:15085744 C ENSESTG00000020862 ENSESTT00000052766 Transcript intron_variant - - - - - - rs1300449 16:15617774 C CCDS45422.1 CCDS45422.1 Transcript intron_variant - - - - - - rs1300449 16:15617774 C ENSESTG00000021104 ENSESTT00000053027 Transcript intron_variant - - - - - - rs1300449 16:15617774 C 89927 NM_001142469.1 Transcript intron_variant - - - - - - rs1300449 16:15617774 C 89927 NM_033201.2 Transcript intron_variant - - - - - - rs1300449 16:15617774 C ENSESTG00000021104 ENSESTT00000053237 Transcript intron_variant - - - - - - rs1300449 16:15617774 C CCDS10561.1 CCDS10561.1 Transcript intron_variant - - - - - - rs1300449 16:15617774 C ENSESTG00000021874 ENSESTT00000054988 Transcript intron_variant - - - - - - rs1300450 16:15664226 G CCDS45422.1 CCDS45422.1 Transcript intron_variant - - - - - - rs1300450 16:15664226 G ENSESTG00000021104 ENSESTT00000053027 Transcript intron_variant - - - - - - rs1300450 16:15664226 G 89927 NM_001142469.1 Transcript intron_variant - - - - - - rs1300450 16:15664226 G 89927 NM_033201.2 Transcript intron_variant - - - - - - rs1300450 16:15664226 G ENSESTG00000021104 ENSESTT00000053237 Transcript intron_variant - - - - - - rs1300450 16:15664226 G CCDS10561.1 CCDS10561.1 Transcript intron_variant - - - - - - rs1300450 16:15664226 G ENSESTG00000021874 ENSESTT00000054988 Transcript intron_variant - - - - - - rs1153866 16:16184623 C ENSESTG00000006219 ENSESTT00000015780 Transcript downstream_gene_variant - - - - - - DISTANCE=313 rs1153866 16:16184623 C 4363 NM_004996.3 Transcript intron_variant - - - - - - rs1153866 16:16184623 C ENSESTG00000006219 ENSESTT00000015777 Transcript intron_variant - - - - - - rs1153866 16:16184623 C ENSESTG00000006219 ENSESTT00000015716 Transcript downstream_gene_variant - - - - - - DISTANCE=313 rs1153866 16:16184623 C CCDS42122.1 CCDS42122.1 Transcript intron_variant - - - - - - rs1153866 16:16184623 C ENSESTG00000006219 ENSESTT00000015725 Transcript downstream_gene_variant - - - - - - DISTANCE=313 rs7199864 16:16284439 C CCDS10568.1 CCDS10568.1 Transcript intron_variant - - - - - - rs7199864 16:16284439 C 368 NM_001171.5 Transcript intron_variant - - - - - - rs9888827 16:17034004 C - - - intergenic_variant - - - - - - rs8046287 16:17135299 T - - - intergenic_variant - - - - - - rs8051970 16:17186778 C - - - intergenic_variant - - - - - - rs9931481 16:17212927 C ENSESTG00000001171 ENSESTT00000002783 Transcript intron_variant - - - - - - rs9931481 16:17212927 C 64131 NM_022166.3 Transcript intron_variant - - - - - - rs9931481 16:17212927 C CCDS10569.1 CCDS10569.1 Transcript intron_variant - - - - - - rs7186270 16:17374513 C 64131 NM_022166.3 Transcript intron_variant - - - - - - rs7186270 16:17374513 C ENSESTG00000001167 ENSESTT00000002767 Transcript intron_variant - - - - - - rs7186270 16:17374513 C CCDS10569.1 CCDS10569.1 Transcript intron_variant - - - - - - rs1229288 16:18007392 C - - - intergenic_variant - - - - - - rs12598312 16:18944278 T - ENSR00001504076 RegulatoryFeature regulatory_region_variant - - - - - - rs12598312 16:18944278 T - - - intergenic_variant - - - - - - rs4381586 16:19041491 C CCDS10573.1 CCDS10573.1 Transcript intron_variant - - - - - - rs4381586 16:19041491 C 79905 NM_024847.3 Transcript intron_variant - - - - - - rs4381586 16:19041491 C 79905 NM_001160364.1 Transcript intron_variant - - - - - - rs4381586 16:19041491 C ENSESTG00000029649 ENSESTT00000074664 Transcript intron_variant - - - - - - rs4381586 16:19041491 C CCDS53992.1 CCDS53992.1 Transcript intron_variant - - - - - - rs10221011 16:19239718 C - ENSR00001504096 RegulatoryFeature regulatory_region_variant - - - - - - rs10221011 16:19239718 C ENSESTG00000016316 ENSESTT00000040945 Transcript intron_variant - - - - - - rs10221011 16:19239718 C CCDS10575.1 CCDS10575.1 Transcript intron_variant - - - - - - rs10221011 16:19239718 C 51760 NM_016524.2 Transcript intron_variant - - - - - - rs10221011 16:19239718 C ENSESTG00000016316 ENSESTT00000040969 Transcript intron_variant - - - - - - rs7498537 16:19912377 C - - - intergenic_variant - - - - - - rs12920367 16:19914022 A - - - intergenic_variant - - - - - - rs10852239 16:20314991 G - - - intergenic_variant - - - - - - rs234282 16:20797191 T CCDS10589.1 CCDS10589.1 Transcript intron_variant - - - - - - rs234282 16:20797191 T CCDS45435.1 CCDS45435.1 Transcript intron_variant - - - - - - rs234282 16:20797191 T ENSESTG00000004705 ENSESTT00000011973 Transcript intron_variant - - - - - - rs234282 16:20797191 T ENSESTG00000004756 ENSESTT00000012049 Transcript downstream_gene_variant - - - - - - DISTANCE=4969 rs234282 16:20797191 T 6296 NM_202000.2 Transcript intron_variant - - - - - - rs234282 16:20797191 T ENSESTG00000004705 ENSESTT00000011961 Transcript intron_variant - - - - - - rs234282 16:20797191 T CCDS10590.1 CCDS10590.1 Transcript intron_variant - - - - - - rs234282 16:20797191 T ENSESTG00000004705 ENSESTT00000011970 Transcript intron_variant - - - - - - rs234282 16:20797191 T 6296 NM_005622.3 Transcript intron_variant - - - - - - rs234282 16:20797191 T ENSESTG00000004705 ENSESTT00000011964 Transcript intron_variant - - - - - - rs234282 16:20797191 T ENSESTG00000004705 ENSESTT00000011971 Transcript intron_variant - - - - - - rs234282 16:20797191 T 112479 NM_080663.2 Transcript intron_variant - - - - - - rs234282 16:20797191 T ENSESTG00000004705 ENSESTT00000011984 Transcript upstream_gene_variant - - - - - - DISTANCE=4716 rs234282 16:20797191 T ENSESTG00000004705 ENSESTT00000011980 Transcript intron_variant - - - - - - rs234282 16:20797191 T ENSESTG00000004705 ENSESTT00000011983 Transcript upstream_gene_variant - - - - - - DISTANCE=4716 rs3095922 16:21030897 C 55567 NM_017539.1 Transcript intron_variant - - - - - - rs3095922 16:21030897 C CCDS10594.1 CCDS10594.1 Transcript intron_variant - - - - - - rs2194057 16:21107287 T 55567 NM_017539.1 Transcript intron_variant - - - - - - rs2194057 16:21107287 T CCDS10594.1 CCDS10594.1 Transcript intron_variant - - - - - - rs2965806 16:21963301 A 7385 NM_003366.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1308 rs2965806 16:21963301 A ENSESTG00000020743 ENSESTT00000052373 Transcript upstream_gene_variant - - - - - - DISTANCE=1318 rs2965806 16:21963301 A ENSESTG00000020743 ENSESTT00000052391 Transcript upstream_gene_variant - - - - - - DISTANCE=1318 rs2965806 16:21963301 A CCDS10601.1 CCDS10601.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1444 rs2965806 16:21963301 A ENSESTG00000020743 ENSESTT00000052350 Transcript upstream_gene_variant - - - - - - DISTANCE=1318 rs8053124 16:22026025 G - ENSR00001504267 RegulatoryFeature regulatory_region_variant - - - - - - rs8053124 16:22026025 G ENSESTG00000020899 ENSESTT00000052437 Transcript intron_variant - - - - - - rs8053124 16:22026025 G ENSESTG00000020899 ENSESTT00000052488 Transcript intron_variant - - - - - - rs8053124 16:22026025 G ENSESTG00000020899 ENSESTT00000052411 Transcript intron_variant - - - - - - rs8053124 16:22026025 G CCDS58431.1 CCDS58431.1 Transcript intron_variant - - - - - - rs8053124 16:22026025 G 730094 NM_001164579.1 Transcript intron_variant - - - - - - rs2550774 16:22762779 A - - - intergenic_variant - - - - - - rs208938 16:22867437 G CCDS10606.1 CCDS10606.1 Transcript intron_variant - - - - - - rs208938 16:22867437 G 9956 NM_006043.1 Transcript intron_variant - - - - - - rs4968017 16:23539946 G ENSESTG00000002991 ENSESTT00000007442 Transcript downstream_gene_variant - - - - - - DISTANCE=4297 rs4968017 16:23539946 G CCDS42132.1 CCDS42132.1 Transcript intron_variant - - - - - - rs4968017 16:23539946 G 124454 NM_001083614.1 Transcript intron_variant - - - - - - rs4968017 16:23539946 G ENSESTG00000003087 ENSESTT00000007702 Transcript downstream_gene_variant - - - - - - DISTANCE=1219 rs4968017 16:23539946 G 124454 NR_003501.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs152461 16:23572802 A ENSESTG00000002999 ENSESTT00000007457 Transcript intron_variant - - - - - - rs152461 16:23572802 A 124454 NM_001083614.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4106 rs152461 16:23572802 A ENSESTG00000003087 ENSESTT00000007702 Transcript upstream_gene_variant - - - - - - DISTANCE=4117 rs152461 16:23572802 A 124454 NR_003501.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4106 rs152461 16:23572802 A ENSESTG00000002999 ENSESTT00000007459 Transcript missense_variant 289 94 32 E/K Gaa/Aaa - rs152461 16:23572802 A CCDS10613.2 CCDS10613.2 Transcript intron_variant - - - - - - rs152461 16:23572802 A CCDS42132.1 CCDS42132.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4138 rs152461 16:23572802 A 56061 NM_019116.2 Transcript intron_variant - - - - - - rs152461 16:23572802 A ENSESTG00000002999 ENSESTT00000007472 Transcript upstream_gene_variant - - - - - - DISTANCE=3085 rs249936 16:23625463 T 79728 NM_024675.3 Transcript intron_variant - - - - - - rs249936 16:23625463 T CCDS32406.1 CCDS32406.1 Transcript intron_variant - - - - - - rs249936 16:23625463 T ENSESTG00000003039 ENSESTT00000007577 Transcript intron_variant - - - - - - rs249936 16:23625463 T ENSESTG00000003039 ENSESTT00000007591 Transcript intron_variant - - - - - - rs249936 16:23625463 T ENSESTG00000003039 ENSESTT00000007583 Transcript intron_variant - - - - - - rs26761 16:23712661 T - ENSR00000665107 RegulatoryFeature regulatory_region_variant - - - - - - rs26761 16:23712661 T CCDS32407.1 CCDS32407.1 Transcript intron_variant - - - - - - rs26761 16:23712661 T 10595 NM_033266.3 Transcript intron_variant - - - - - - rs40138 16:23715230 A CCDS32407.1 CCDS32407.1 Transcript intron_variant - - - - - - rs40138 16:23715230 A 10595 NM_033266.3 Transcript intron_variant - - - - - - rs174216 16:23781534 A - - - intergenic_variant - - - - - - rs2575391 16:23818180 A - - - intergenic_variant - - - - - - rs195998 16:23956891 G 5579 NM_212535.2 Transcript intron_variant - - - - - - rs195998 16:23956891 G 5579 NM_002738.6 Transcript intron_variant - - - - - - rs195998 16:23956891 G CCDS10618.1 CCDS10618.1 Transcript intron_variant - - - - - - rs195998 16:23956891 G CCDS10619.1 CCDS10619.1 Transcript intron_variant - - - - - - rs195998 16:23956891 G ENSESTG00000014245 ENSESTT00000035655 Transcript intron_variant - - - - - - rs271004 16:24532188 G - - - intergenic_variant - - - - - - rs274081 16:24902194 C 115584 NM_052944.3 Transcript synonymous_variant 901 669 223 F ttT/ttC - rs274081 16:24902194 C CCDS10625.1 CCDS10625.1 Transcript synonymous_variant 669 669 223 F ttT/ttC - rs274081 16:24902194 C 115584 NM_001258412.1 Transcript synonymous_variant 840 459 153 F ttT/ttC - rs274081 16:24902194 C CCDS58439.1 CCDS58439.1 Transcript synonymous_variant 477 477 159 F ttT/ttC - rs274081 16:24902194 C 115584 NM_001258414.1 Transcript intron_variant - - - - - - rs274081 16:24902194 C ENSESTG00000028138 ENSESTT00000070744 Transcript synonymous_variant 346 186 62 F ttT/ttC - rs274081 16:24902194 C CCDS58440.1 CCDS58440.1 Transcript intron_variant - - - - - - rs274081 16:24902194 C CCDS58438.1 CCDS58438.1 Transcript synonymous_variant 459 459 153 F ttT/ttC - rs274081 16:24902194 C 115584 NM_001258411.1 Transcript synonymous_variant 945 564 188 F ttT/ttC - rs274081 16:24902194 C 115584 NM_001258413.1 Transcript synonymous_variant 891 477 159 F ttT/ttC - rs274081 16:24902194 C CCDS58437.1 CCDS58437.1 Transcript synonymous_variant 564 564 188 F ttT/ttC - rs4787303 16:25132973 G ENSESTG00000028209 ENSESTT00000071157 Transcript intron_variant - - - - - - rs4787303 16:25132973 G ENSESTG00000028209 ENSESTT00000071139 Transcript intron_variant - - - - - - rs4787303 16:25132973 G 51451 NM_016309.2 Transcript intron_variant - - - - - - rs4787303 16:25132973 G 51451 NM_001032391.1 Transcript intron_variant - - - - - - rs4787303 16:25132973 G ENSESTG00000028209 ENSESTT00000071148 Transcript intron_variant - - - - - - rs4787303 16:25132973 G CCDS45446.1 CCDS45446.1 Transcript intron_variant - - - - - - rs4787303 16:25132973 G CCDS45445.1 CCDS45445.1 Transcript intron_variant - - - - - - rs4787303 16:25132973 G ENSESTG00000028209 ENSESTT00000071086 Transcript intron_variant - - - - - - rs4787303 16:25132973 G ENSESTG00000028209 ENSESTT00000071103 Transcript intron_variant - - - - - - rs205166 16:25591994 A - - - intergenic_variant - - - - - - rs2157860 16:26408477 C - ENSR00000665147 RegulatoryFeature regulatory_region_variant - - - - - - rs2157860 16:26408477 C - - - intergenic_variant - - - - - - rs9302442 16:26456758 G - - - intergenic_variant - - - - - - rs4787839 16:26467306 C - - - intergenic_variant - - - - - - rs982685 16:26538423 T - - - intergenic_variant - - - - - - rs1895386 16:26560988 T - - - intergenic_variant - - - - - - rs211497 16:26791514 G - - - intergenic_variant - - - - - - rs4238944 16:26967283 C - - - intergenic_variant - - - - - - rs4261543 16:26980465 T - - - intergenic_variant - - - - - - rs7191819 16:27036960 A - - - intergenic_variant - - - - - - rs233452 16:27641851 G ENSESTG00000015854 ENSESTT00000039806 Transcript intron_variant - - - - - - rs233452 16:27641851 G ENSESTG00000015854 ENSESTT00000039795 Transcript intron_variant - - - - - - rs233452 16:27641851 G 23247 NM_015202.2 Transcript intron_variant - - - - - - rs233452 16:27641851 G ENSESTG00000015854 ENSESTT00000039801 Transcript intron_variant - - - - - - rs233452 16:27641851 G CCDS32415.1 CCDS32415.1 Transcript intron_variant - - - - - - rs6498033 16:27713298 A ENSESTG00000015854 ENSESTT00000039795 Transcript intron_variant - - - - - - rs6498033 16:27713298 A 23247 NM_015202.2 Transcript intron_variant - - - - - - rs6498033 16:27713298 A ENSESTG00000015854 ENSESTT00000039801 Transcript intron_variant - - - - - - rs6498033 16:27713298 A CCDS32415.1 CCDS32415.1 Transcript intron_variant - - - - - - rs1645337 16:27829696 T 146395 NM_144675.2 Transcript intron_variant - - - - - - rs1645337 16:27829696 T ENSESTG00000021517 ENSESTT00000053996 Transcript intron_variant - - - - - - rs1645337 16:27829696 T CCDS10631.1 CCDS10631.1 Transcript intron_variant - - - - - - rs1645337 16:27829696 T CCDS45450.1 CCDS45450.1 Transcript intron_variant - - - - - - rs1645337 16:27829696 T 146395 NM_001109763.1 Transcript intron_variant - - - - - - rs176109 16:28089616 G - - - intergenic_variant - - - - - - rs28379290 16:28157351 C 23214 NM_015171.2 Transcript intron_variant - - - - - - rs28379290 16:28157351 C CCDS42135.1 CCDS42135.1 Transcript intron_variant - - - - - - rs28379290 16:28157351 C ENSESTG00000021414 ENSESTT00000053720 Transcript intron_variant - - - - - - rs252492 16:29158961 G ENSESTG00000003065 ENSESTT00000007661 Transcript intron_variant - - - - - - rs252492 16:29158961 G ENSESTG00000003065 ENSESTT00000007656 Transcript intron_variant - - - - - - rs235637 16:29791561 G ENSESTG00000024740 ENSESTT00000062579 Transcript missense_variant 399 325 109 L/V Tta/Gta - PolyPhen=benign;SIFT=tolerated rs235637 16:29791561 G CCDS54000.1 CCDS54000.1 Transcript missense_variant 325 325 109 L/V Tta/Gta - PolyPhen=benign;SIFT=tolerated rs235637 16:29791561 G 653808 NM_152338.3 Transcript missense_variant 399 325 109 L/V Tta/Gta - PolyPhen=benign;SIFT=tolerated rs8051470 16:29905677 C CCDS45458.1 CCDS45458.1 Transcript intron_variant - - - - - - rs8051470 16:29905677 C ENSESTG00000015694 ENSESTT00000039431 Transcript intron_variant - - - - - - rs8051470 16:29905677 C ENSESTG00000015694 ENSESTT00000039368 Transcript intron_variant - - - - - - rs8051470 16:29905677 C CCDS10659.1 CCDS10659.1 Transcript intron_variant - - - - - - rs8051470 16:29905677 C 26470 NM_012410.3 Transcript intron_variant - - - - - - rs8051470 16:29905677 C ENSESTG00000015694 ENSESTT00000039436 Transcript intron_variant - - - - - - rs8051470 16:29905677 C 26470 NM_001114100.2 Transcript intron_variant - - - - - - rs8051470 16:29905677 C 26470 NM_001243332.1 Transcript intron_variant - - - - - - rs8051470 16:29905677 C 26470 NM_201575.3 Transcript intron_variant - - - - - - rs8051470 16:29905677 C ENSESTG00000015694 ENSESTT00000039423 Transcript intron_variant - - - - - - rs8051470 16:29905677 C ENSESTG00000015694 ENSESTT00000039417 Transcript intron_variant - - - - - - rs8051470 16:29905677 C ENSESTG00000015694 ENSESTT00000039438 Transcript intron_variant - - - - - - rs8051470 16:29905677 C ENSESTG00000015694 ENSESTT00000039406 Transcript intron_variant - - - - - - rs8051470 16:29905677 C ENSESTG00000015694 ENSESTT00000039439 Transcript intron_variant - - - - - - rs8051470 16:29905677 C 26470 NM_001114099.2 Transcript intron_variant - - - - - - rs8051470 16:29905677 C CCDS58447.1 CCDS58447.1 Transcript intron_variant - - - - - - rs8051470 16:29905677 C CCDS10658.1 CCDS10658.1 Transcript intron_variant - - - - - - rs8051470 16:29905677 C 26470 NM_001243333.1 Transcript intron_variant - - - - - - rs6565202 16:30778579 A ENSESTG00000014874 ENSESTT00000037344 Transcript intron_variant - - - - - - rs6565202 16:30778579 A 9810 NM_014771.3 Transcript intron_variant - - - - - - rs6565202 16:30778579 A ENSESTG00000014874 ENSESTT00000037340 Transcript intron_variant - - - - - - rs6565202 16:30778579 A CCDS55994.1 CCDS55994.1 Transcript intron_variant - - - - - - rs6565202 16:30778579 A ENSESTG00000014874 ENSESTT00000037308 Transcript downstream_gene_variant - - - - - - DISTANCE=418 rs6565202 16:30778579 A ENSESTG00000011468 ENSESTT00000028803 Transcript upstream_gene_variant - - - - - - DISTANCE=1680 rs6565202 16:30778579 A 9810 NM_001207034.1 Transcript intron_variant - - - - - - rs6565202 16:30778579 A CCDS10691.1 CCDS10691.1 Transcript intron_variant - - - - - - rs6565202 16:30778579 A ENSESTG00000014874 ENSESTT00000037327 Transcript intron_variant - - - - - - rs6565202 16:30778579 A ENSESTG00000014874 ENSESTT00000037367 Transcript intron_variant - - - - - - rs6565202 16:30778579 A 9810 NM_001207033.1 Transcript intron_variant - - - - - - rs7195142 16:30779716 G ENSESTG00000014874 ENSESTT00000037344 Transcript intron_variant - - - - - - rs7195142 16:30779716 G 9810 NM_014771.3 Transcript missense_variant 2664 1844 615 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs7195142 16:30779716 G ENSESTG00000014874 ENSESTT00000037340 Transcript intron_variant - - - - - - rs7195142 16:30779716 G CCDS55994.1 CCDS55994.1 Transcript missense_variant 1544 1544 515 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs7195142 16:30779716 G ENSESTG00000014874 ENSESTT00000037308 Transcript downstream_gene_variant - - - - - - DISTANCE=1555 rs7195142 16:30779716 G ENSESTG00000011468 ENSESTT00000028803 Transcript upstream_gene_variant - - - - - - DISTANCE=543 rs7195142 16:30779716 G 9810 NM_001207034.1 Transcript missense_variant 2364 1544 515 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs7195142 16:30779716 G CCDS10691.1 CCDS10691.1 Transcript missense_variant 1844 1844 615 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs7195142 16:30779716 G ENSESTG00000014874 ENSESTT00000037327 Transcript intron_variant - - - - - - rs7195142 16:30779716 G ENSESTG00000014874 ENSESTT00000037367 Transcript missense_variant 450 398 133 Q/R cAg/cGg - rs7195142 16:30779716 G 9810 NM_001207033.1 Transcript missense_variant 2664 1844 615 Q/R cAg/cGg - rs4889686 16:30929636 G 283932 NR_024348.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1004 rs8064069 16:31328272 C CCDS54004.1 CCDS54004.1 Transcript intron_variant - - - - - - rs8064069 16:31328272 C ENSESTG00000006841 ENSESTT00000017452 Transcript intron_variant - - - - - - rs8064069 16:31328272 C ENSESTG00000006841 ENSESTT00000017448 Transcript intron_variant - - - - - - rs8064069 16:31328272 C CCDS45470.1 CCDS45470.1 Transcript intron_variant - - - - - - rs8064069 16:31328272 C 3684 NM_000632.3 Transcript intron_variant - - - - - - rs8064069 16:31328272 C 3684 NM_001145808.1 Transcript intron_variant - - - - - - rs7190525 16:31924855 G 10308 NR_049749.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7190525 16:31924855 G ENSESTG00000007486 ENSESTT00000018912 Transcript intron_variant - - - - - - rs7190525 16:31924855 G CCDS32440.1 CCDS32440.1 Transcript intron_variant - - - - - - rs7190525 16:31924855 G 10308 NM_003414.5 Transcript intron_variant - - - - - - rs7190525 16:31924855 G 10308 NM_001265588.1 Transcript intron_variant - - - - - - rs7190525 16:31924855 G ENSESTG00000007486 ENSESTT00000018907 Transcript intron_variant - - - - - - rs6563853 16:34318731 G - - - intergenic_variant - - - - - - rs1872687 16:34381346 G - - - intergenic_variant - - - - - - rs9923818 16:34465885 G ENSESTG00000019508 ENSESTT00000048966 Transcript intron_variant - - - - - - rs9923818 16:34465885 G ENSESTG00000019508 ENSESTT00000048985 Transcript intron_variant - - - - - - rs371861 16:34783452 G - - - intergenic_variant - - - - - - rs345549 16:34799701 T - - - intergenic_variant - - - - - - rs1960806 16:35171474 C - - - intergenic_variant - - - - - - rs4545823 16:35181957 A - - - intergenic_variant - - - - - - rs2939264 16:47301334 C ENSESTG00000009216 ENSESTT00000023188 Transcript intron_variant - - - - - - rs2939264 16:47301334 C ENSESTG00000009216 ENSESTT00000023245 Transcript intron_variant - - - - - - rs2939264 16:47301334 C ENSESTG00000009216 ENSESTT00000023219 Transcript intron_variant - - - - - - rs2939264 16:47301334 C ENSESTG00000009216 ENSESTT00000023185 Transcript intron_variant - - - - - - rs2939264 16:47301334 C CCDS10728.1 CCDS10728.1 Transcript intron_variant - - - - - - rs2939264 16:47301334 C 81533 NM_030790.3 Transcript intron_variant - - - - - - rs2939264 16:47301334 C ENSESTG00000009216 ENSESTT00000023222 Transcript intron_variant - - - - - - rs2939264 16:47301334 C ENSESTG00000009216 ENSESTT00000023243 Transcript intron_variant - - - - - - rs2939264 16:47301334 C ENSESTG00000009216 ENSESTT00000023173 Transcript intron_variant - - - - - - rs2939264 16:47301334 C ENSESTG00000009216 ENSESTT00000023179 Transcript intron_variant - - - - - - rs9937856 16:47345744 G - ENSR00000506998 RegulatoryFeature regulatory_region_variant - - - - - - rs9937856 16:47345744 G ENSESTG00000009216 ENSESTT00000023188 Transcript intron_variant - - - - - - rs9937856 16:47345744 G ENSESTG00000009134 ENSESTT00000022921 Transcript intron_variant - - - - - - rs9937856 16:47345744 G ENSESTG00000009216 ENSESTT00000023245 Transcript intron_variant - - - - - - rs9937856 16:47345744 G ENSESTG00000009216 ENSESTT00000023219 Transcript intron_variant - - - - - - rs9937856 16:47345744 G ENSESTG00000009216 ENSESTT00000023185 Transcript intron_variant - - - - - - rs9937856 16:47345744 G CCDS10728.1 CCDS10728.1 Transcript intron_variant - - - - - - rs9937856 16:47345744 G 81533 NM_030790.3 Transcript intron_variant - - - - - - rs9937856 16:47345744 G ENSESTG00000009216 ENSESTT00000023222 Transcript intron_variant - - - - - - rs9937856 16:47345744 G ENSESTG00000009216 ENSESTT00000023243 Transcript intron_variant - - - - - - rs9937856 16:47345744 G ENSESTG00000009216 ENSESTT00000023173 Transcript intron_variant - - - - - - rs9937856 16:47345744 G ENSESTG00000009216 ENSESTT00000023179 Transcript intron_variant - - - - - - rs28456153 16:47754818 T - - - intergenic_variant - - - - - - rs567437 16:48083449 G - - - intergenic_variant - - - - - - rs2098405 16:49080637 G - - - intergenic_variant - - - - - - rs1558761 16:49082083 A - - - intergenic_variant - - - - - - rs4785330 16:49705890 C CCDS32445.1 CCDS32445.1 Transcript intron_variant - - - - - - rs4785330 16:49705890 C ENSESTG00000031138 ENSESTT00000078411 Transcript intron_variant - - - - - - rs4785330 16:49705890 C ENSESTG00000031138 ENSESTT00000078498 Transcript intron_variant - - - - - - rs4785330 16:49705890 C 23090 NM_015069.2 Transcript intron_variant - - - - - - rs8049248 16:49706987 C - ENSR00001504997 RegulatoryFeature regulatory_region_variant - - - - - - rs8049248 16:49706987 C CCDS32445.1 CCDS32445.1 Transcript intron_variant - - - - - - rs8049248 16:49706987 C ENSESTG00000031138 ENSESTT00000078411 Transcript intron_variant - - - - - - rs8049248 16:49706987 C ENSESTG00000031138 ENSESTT00000078498 Transcript intron_variant - - - - - - rs8049248 16:49706987 C 23090 NM_015069.2 Transcript intron_variant - - - - - - rs8057822 16:49822726 C CCDS32445.1 CCDS32445.1 Transcript intron_variant - - - - - - rs8057822 16:49822726 C ENSESTG00000031138 ENSESTT00000078411 Transcript intron_variant - - - - - - rs8057822 16:49822726 C ENSESTG00000031138 ENSESTT00000078425 Transcript intron_variant - - - - - - rs8057822 16:49822726 C ENSESTG00000031138 ENSESTT00000078514 Transcript intron_variant - - - - - - rs8057822 16:49822726 C ENSESTG00000031138 ENSESTT00000078498 Transcript intron_variant - - - - - - rs8057822 16:49822726 C 23090 NM_015069.2 Transcript intron_variant - - - - - - rs6500275 16:50028796 T - - - intergenic_variant - - - - - - rs8056175 16:50032097 G - - - intergenic_variant - - - - - - rs6500278 16:50053409 T - - - intergenic_variant - - - - - - rs11864023 16:50064372 A 255919 NM_153261.4 Transcript intron_variant - - - - - - rs11864023 16:50064372 A ENSESTG00000030702 ENSESTT00000077316 Transcript intron_variant - - - - - - rs11864023 16:50064372 A ENSESTG00000030702 ENSESTT00000077304 Transcript intron_variant - - - - - - rs11864023 16:50064372 A ENSESTG00000030702 ENSESTT00000077325 Transcript intron_variant - - - - - - rs11864023 16:50064372 A CCDS45480.1 CCDS45480.1 Transcript intron_variant - - - - - - rs7206346 16:50074846 C 255919 NM_153261.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3847 rs7206346 16:50074846 C ENSESTG00000030702 ENSESTT00000077316 Transcript downstream_gene_variant - - - - - - DISTANCE=4996 rs7206346 16:50074846 C ENSESTG00000030702 ENSESTT00000077304 Transcript downstream_gene_variant - - - - - - DISTANCE=4996 rs7206346 16:50074846 C ENSESTG00000030702 ENSESTT00000077325 Transcript downstream_gene_variant - - - - - - DISTANCE=4996 rs1420690 16:50075206 T 255919 NM_153261.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4207 rs2356834 16:50087087 G - - - intergenic_variant - - - - - - rs9924751 16:50110742 C ENSESTG00000030729 ENSESTT00000077546 Transcript downstream_gene_variant - - - - - - DISTANCE=4154 rs9924751 16:50110742 C ENSESTG00000030729 ENSESTT00000077492 Transcript intron_variant - - - - - - rs9924751 16:50110742 C ENSESTG00000030729 ENSESTT00000077522 Transcript downstream_gene_variant - - - - - - DISTANCE=4204 rs9924751 16:50110742 C ENSESTG00000030729 ENSESTT00000077593 Transcript upstream_gene_variant - - - - - - DISTANCE=3201 rs9924751 16:50110742 C ENSESTG00000030729 ENSESTT00000077570 Transcript intron_variant - - - - - - rs9924751 16:50110742 C ENSESTG00000030729 ENSESTT00000077591 Transcript upstream_gene_variant - - - - - - DISTANCE=2113 rs9924751 16:50110742 C 55027 NM_182922.2 Transcript intron_variant - - - - - - rs9924751 16:50110742 C CCDS10739.1 CCDS10739.1 Transcript intron_variant - - - - - - rs1894971 16:50116305 G ENSESTG00000030729 ENSESTT00000077570 Transcript intron_variant - - - - - - rs1894971 16:50116305 G ENSESTG00000030729 ENSESTT00000077591 Transcript intron_variant - - - - - - rs1894971 16:50116305 G ENSESTG00000030729 ENSESTT00000077492 Transcript intron_variant - - - - - - rs1894971 16:50116305 G ENSESTG00000030729 ENSESTT00000077597 Transcript upstream_gene_variant - - - - - - DISTANCE=1533 rs1894971 16:50116305 G CCDS10739.1 CCDS10739.1 Transcript intron_variant - - - - - - rs1894971 16:50116305 G ENSESTG00000030729 ENSESTT00000077593 Transcript intron_variant - - - - - - rs1894971 16:50116305 G 55027 NM_182922.2 Transcript intron_variant - - - - - - rs8062520 16:50124723 C ENSESTG00000030729 ENSESTT00000077570 Transcript intron_variant - - - - - - rs8062520 16:50124723 C ENSESTG00000030729 ENSESTT00000077591 Transcript intron_variant - - - - - - rs8062520 16:50124723 C ENSESTG00000030729 ENSESTT00000077492 Transcript intron_variant - - - - - - rs8062520 16:50124723 C ENSESTG00000030729 ENSESTT00000077597 Transcript intron_variant - - - - - - rs8062520 16:50124723 C CCDS10739.1 CCDS10739.1 Transcript intron_variant - - - - - - rs8062520 16:50124723 C ENSESTG00000030729 ENSESTT00000077593 Transcript intron_variant - - - - - - rs8062520 16:50124723 C 55027 NM_182922.2 Transcript intron_variant - - - - - - rs1477127 16:50125383 A ENSESTG00000030729 ENSESTT00000077570 Transcript intron_variant - - - - - - rs1477127 16:50125383 A ENSESTG00000030729 ENSESTT00000077591 Transcript intron_variant - - - - - - rs1477127 16:50125383 A ENSESTG00000030729 ENSESTT00000077492 Transcript intron_variant - - - - - - rs1477127 16:50125383 A ENSESTG00000030729 ENSESTT00000077597 Transcript intron_variant - - - - - - rs1477127 16:50125383 A CCDS10739.1 CCDS10739.1 Transcript intron_variant - - - - - - rs1477127 16:50125383 A ENSESTG00000030729 ENSESTT00000077593 Transcript intron_variant - - - - - - rs1477127 16:50125383 A 55027 NM_182922.2 Transcript intron_variant - - - - - - rs7195793 16:50125922 C ENSESTG00000030729 ENSESTT00000077570 Transcript intron_variant - - - - - - rs7195793 16:50125922 C ENSESTG00000030729 ENSESTT00000077591 Transcript intron_variant - - - - - - rs7195793 16:50125922 C ENSESTG00000030729 ENSESTT00000077492 Transcript intron_variant - - - - - - rs7195793 16:50125922 C ENSESTG00000030729 ENSESTT00000077597 Transcript intron_variant - - - - - - rs7195793 16:50125922 C CCDS10739.1 CCDS10739.1 Transcript intron_variant - - - - - - rs7195793 16:50125922 C ENSESTG00000030729 ENSESTT00000077593 Transcript intron_variant - - - - - - rs7195793 16:50125922 C 55027 NM_182922.2 Transcript intron_variant - - - - - - rs8062149 16:50130500 A ENSESTG00000030729 ENSESTT00000077570 Transcript intron_variant - - - - - - rs8062149 16:50130500 A ENSESTG00000030729 ENSESTT00000077591 Transcript intron_variant - - - - - - rs8062149 16:50130500 A ENSESTG00000030729 ENSESTT00000077492 Transcript intron_variant - - - - - - rs8062149 16:50130500 A ENSESTG00000030729 ENSESTT00000077597 Transcript intron_variant - - - - - - rs8062149 16:50130500 A CCDS10739.1 CCDS10739.1 Transcript intron_variant - - - - - - rs8062149 16:50130500 A ENSESTG00000030729 ENSESTT00000077593 Transcript intron_variant - - - - - - rs8062149 16:50130500 A 55027 NM_182922.2 Transcript intron_variant - - - - - - rs4302029 16:50165925 A - - - intergenic_variant - - - - - - rs2160569 16:50189761 A - ENSR00001505032 RegulatoryFeature regulatory_region_variant - - - - - - rs2160569 16:50189761 A ENSESTG00000030818 ENSESTT00000077748 Transcript intron_variant - - - - - - rs2160569 16:50189761 A 64282 NM_001040284.2 Transcript intron_variant - - - - - - rs2160569 16:50189761 A CCDS54006.1 CCDS54006.1 Transcript intron_variant - - - - - - rs2160569 16:50189761 A 64282 NM_001040285.2 Transcript intron_variant - - - - - - rs2160569 16:50189761 A ENSESTG00000031130 ENSESTT00000078373 Transcript intron_variant - - - - - - rs4785388 16:50191178 G ENSESTG00000030818 ENSESTT00000077748 Transcript intron_variant - - - - - - rs4785388 16:50191178 G 64282 NM_001040284.2 Transcript intron_variant - - - - - - rs4785388 16:50191178 G CCDS54006.1 CCDS54006.1 Transcript intron_variant - - - - - - rs4785388 16:50191178 G 64282 NM_001040285.2 Transcript intron_variant - - - - - - rs4785388 16:50191178 G ENSESTG00000031130 ENSESTT00000078373 Transcript intron_variant - - - - - - rs4785390 16:50192363 T ENSESTG00000030818 ENSESTT00000077748 Transcript intron_variant - - - - - - rs4785390 16:50192363 T 64282 NM_001040284.2 Transcript intron_variant - - - - - - rs4785390 16:50192363 T CCDS54006.1 CCDS54006.1 Transcript intron_variant - - - - - - rs4785390 16:50192363 T 64282 NM_001040285.2 Transcript intron_variant - - - - - - rs4785390 16:50192363 T ENSESTG00000031130 ENSESTT00000078373 Transcript intron_variant - - - - - - rs6500295 16:50202612 A ENSESTG00000030818 ENSESTT00000077748 Transcript intron_variant - - - - - - rs6500295 16:50202612 A 64282 NM_001040284.2 Transcript intron_variant - - - - - - rs6500295 16:50202612 A CCDS54006.1 CCDS54006.1 Transcript intron_variant - - - - - - rs6500295 16:50202612 A 64282 NM_001040285.2 Transcript intron_variant - - - - - - rs6500295 16:50202612 A ENSESTG00000031130 ENSESTT00000078373 Transcript intron_variant - - - - - - rs6500296 16:50202801 C ENSESTG00000030818 ENSESTT00000077748 Transcript intron_variant - - - - - - rs6500296 16:50202801 C 64282 NM_001040284.2 Transcript intron_variant - - - - - - rs6500296 16:50202801 C CCDS54006.1 CCDS54006.1 Transcript intron_variant - - - - - - rs6500296 16:50202801 C 64282 NM_001040285.2 Transcript intron_variant - - - - - - rs6500296 16:50202801 C ENSESTG00000031130 ENSESTT00000078373 Transcript intron_variant - - - - - - rs6500299 16:50240122 A ENSESTG00000030818 ENSESTT00000077748 Transcript intron_variant - - - - - - rs6500299 16:50240122 A 64282 NM_001040284.2 Transcript intron_variant - - - - - - rs6500299 16:50240122 A CCDS54006.1 CCDS54006.1 Transcript intron_variant - - - - - - rs6500299 16:50240122 A 64282 NM_001040285.2 Transcript intron_variant - - - - - - rs6500299 16:50240122 A ENSESTG00000031130 ENSESTT00000078373 Transcript intron_variant - - - - - - rs7204079 16:50241006 A ENSESTG00000030818 ENSESTT00000077748 Transcript intron_variant - - - - - - rs7204079 16:50241006 A 64282 NM_001040284.2 Transcript intron_variant - - - - - - rs7204079 16:50241006 A CCDS54006.1 CCDS54006.1 Transcript intron_variant - - - - - - rs7204079 16:50241006 A 64282 NM_001040285.2 Transcript intron_variant - - - - - - rs7204079 16:50241006 A ENSESTG00000031130 ENSESTT00000078373 Transcript intron_variant - - - - - - rs4624170 16:50261735 T ENSESTG00000030818 ENSESTT00000077748 Transcript intron_variant - - - - - - rs4624170 16:50261735 T 64282 NM_001040284.2 Transcript intron_variant - - - - - - rs4624170 16:50261735 T CCDS54006.1 CCDS54006.1 Transcript intron_variant - - - - - - rs4624170 16:50261735 T 64282 NM_001040285.2 Transcript intron_variant - - - - - - rs4624170 16:50261735 T ENSESTG00000031130 ENSESTT00000078373 Transcript intron_variant - - - - - - rs7200997 16:50287703 G - ENSR00000272283 RegulatoryFeature regulatory_region_variant - - - - - - rs7200997 16:50287703 G - - - intergenic_variant - - - - - - rs4578645 16:50299568 C - ENSR00001505047 RegulatoryFeature regulatory_region_variant - - - - - - rs4578645 16:50299568 C ENSESTG00000030880 ENSESTT00000077781 Transcript upstream_gene_variant - - - - - - DISTANCE=859 rs4578645 16:50299568 C ENSESTG00000030880 ENSESTT00000077834 Transcript upstream_gene_variant - - - - - - DISTANCE=883 rs4578645 16:50299568 C ENSESTG00000030880 ENSESTT00000077843 Transcript upstream_gene_variant - - - - - - DISTANCE=907 rs7186289 16:50364510 G 29117 NM_013263.4 Transcript intron_variant - - - - - - rs7186289 16:50364510 G CCDS10742.1 CCDS10742.1 Transcript intron_variant - - - - - - rs7186289 16:50364510 G 29117 NM_001173984.2 Transcript intron_variant - - - - - - rs7186289 16:50364510 G CCDS54007.1 CCDS54007.1 Transcript intron_variant - - - - - - rs7186289 16:50364510 G ENSESTG00000031042 ENSESTT00000078356 Transcript intron_variant - - - - - - rs4569279 16:50369895 A 29117 NM_013263.4 Transcript intron_variant - - - - - - rs4569279 16:50369895 A CCDS10742.1 CCDS10742.1 Transcript intron_variant - - - - - - rs4569279 16:50369895 A 29117 NM_001173984.2 Transcript intron_variant - - - - - - rs4569279 16:50369895 A CCDS54007.1 CCDS54007.1 Transcript intron_variant - - - - - - rs4569279 16:50369895 A ENSESTG00000031042 ENSESTT00000078181 Transcript downstream_gene_variant - - - - - - DISTANCE=3988 rs4569279 16:50369895 A ENSESTG00000031042 ENSESTT00000078356 Transcript intron_variant - - - - - - rs4407056 16:50388657 A 29117 NM_013263.4 Transcript intron_variant - - - - - - rs4407056 16:50388657 A CCDS10742.1 CCDS10742.1 Transcript intron_variant - - - - - - rs4407056 16:50388657 A 29117 NM_001173984.2 Transcript intron_variant - - - - - - rs4407056 16:50388657 A CCDS54007.1 CCDS54007.1 Transcript intron_variant - - - - - - rs4407056 16:50388657 A ENSESTG00000031042 ENSESTT00000078181 Transcript intron_variant - - - - - - rs4407056 16:50388657 A ENSESTG00000031042 ENSESTT00000078356 Transcript intron_variant - - - - - - rs1861541 16:50394445 G - ENSR00001505058 RegulatoryFeature regulatory_region_variant - - - - - - rs1861541 16:50394445 G 29117 NM_013263.4 Transcript intron_variant - - - - - - rs1861541 16:50394445 G CCDS10742.1 CCDS10742.1 Transcript intron_variant - - - - - - rs1861541 16:50394445 G 29117 NM_001173984.2 Transcript intron_variant - - - - - - rs1861541 16:50394445 G CCDS54007.1 CCDS54007.1 Transcript intron_variant - - - - - - rs1861541 16:50394445 G ENSESTG00000031042 ENSESTT00000078181 Transcript intron_variant - - - - - - rs1861541 16:50394445 G ENSESTG00000031042 ENSESTT00000078356 Transcript intron_variant - - - - - - rs6500314 16:50460400 C - - - intergenic_variant - - - - - - rs11076539 16:50705403 G ENSESTG00000024183 ENSESTT00000061103 Transcript 3_prime_UTR_variant 379 - - - - - rs11076539 16:50705403 G CCDS45481.1 CCDS45481.1 Transcript intron_variant - - - - - - rs11076539 16:50705403 G ENSESTG00000024172 ENSESTT00000061088 Transcript downstream_gene_variant - - - - - - DISTANCE=612 rs11076539 16:50705403 G 124460 NM_153337.2 Transcript intron_variant - - - - - - rs11076539 16:50705403 G ENSESTG00000024469 ENSESTT00000061944 Transcript downstream_gene_variant - - - - - - DISTANCE=2433 rs11076539 16:50705403 G ENSESTG00000024188 ENSESTT00000061112 Transcript upstream_gene_variant - - - - - - DISTANCE=176 rs11076539 16:50705403 G 124460 NM_182854.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1483 rs11076539 16:50705403 G 124460 NM_001144972.1 Transcript intron_variant - - - - - - rs11076539 16:50705403 G ENSESTG00000024469 ENSESTT00000061928 Transcript intron_variant - - - - - - rs11076539 16:50705403 G CCDS10744.1 CCDS10744.1 Transcript intron_variant - - - - - - rs11076539 16:50705403 G CCDS10745.1 CCDS10745.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1914 rs7197859 16:50846810 G - - - intergenic_variant - - - - - - rs6416793 16:51073133 C ENSESTG00000024395 ENSESTT00000061721 Transcript downstream_gene_variant - - - - - - DISTANCE=3450 rs6416793 16:51073133 C ENSESTG00000024395 ENSESTT00000061698 Transcript downstream_gene_variant - - - - - - DISTANCE=3443 rs1079561 16:51476991 T - - - intergenic_variant - - - - - - rs2386962 16:51906240 C - - - intergenic_variant - - - - - - rs12446912 16:51907130 G - - - intergenic_variant - - - - - - rs2193089 16:51936588 A - - - intergenic_variant - - - - - - rs33340 16:52035764 G - - - intergenic_variant - - - - - - rs254176 16:52049011 C - - - intergenic_variant - - - - - - rs1111476 16:52174441 A - - - intergenic_variant - - - - - - rs1833181 16:52241675 T ENSESTG00000004678 ENSESTT00000011786 Transcript intron_variant - - - - - - rs3859087 16:52329063 A - - - intergenic_variant - - - - - - rs1421089 16:53869213 G CCDS32448.1 CCDS32448.1 Transcript intron_variant - - - - - - rs1421089 16:53869213 G 79068 NM_001080432.2 Transcript intron_variant - - - - - - rs1389526 16:54663765 G - - - intergenic_variant - - - - - - rs1948463 16:54674843 G - - - intergenic_variant - - - - - - rs2576535 16:55481488 G ENSESTG00000026972 ENSESTT00000067992 Transcript upstream_gene_variant - - - - - - DISTANCE=2817 rs2576529 16:55483289 C ENSESTG00000026972 ENSESTT00000067992 Transcript upstream_gene_variant - - - - - - DISTANCE=4618 rs1815988 16:55925667 C CCDS54012.1 CCDS54012.1 Transcript intron_variant - - - - - - rs1815988 16:55925667 C 221223 NM_001190158.1 Transcript intron_variant - - - - - - rs1815988 16:55925667 C ENSESTG00000002391 ENSESTT00000005934 Transcript intron_variant - - - - - - rs28451741 16:55941475 G CCDS54012.1 CCDS54012.1 Transcript intron_variant - - - - - - rs28451741 16:55941475 G 221223 NM_001190158.1 Transcript intron_variant - - - - - - rs28451741 16:55941475 G ENSESTG00000002391 ENSESTT00000005934 Transcript intron_variant - - - - - - rs8044185 16:56068717 T - - - intergenic_variant - - - - - - rs4784627 16:56084610 C - - - intergenic_variant - - - - - - rs1510190 16:56099559 A - - - intergenic_variant - - - - - - rs8055519 16:56103430 G - - - intergenic_variant - - - - - - rs9934302 16:56152469 C ENSESTG00000002192 ENSESTT00000005492 Transcript upstream_gene_variant - - - - - - DISTANCE=3367 rs9934302 16:56152469 C 283856 NR_027078.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9934302 16:56152469 C ENSESTG00000002388 ENSESTT00000005925 Transcript intron_variant - - - - - - rs899238 16:56323508 G 2775 NM_020988.2 Transcript intron_variant - - - - - - rs899238 16:56323508 G ENSESTG00000002198 ENSESTT00000005552 Transcript intron_variant - - - - - - rs899238 16:56323508 G CCDS10756.1 CCDS10756.1 Transcript intron_variant - - - - - - rs899238 16:56323508 G CCDS10757.1 CCDS10757.1 Transcript intron_variant - - - - - - rs899238 16:56323508 G 2775 NM_138736.2 Transcript intron_variant - - - - - - rs6499835 16:56442762 G - ENSR00000507910 RegulatoryFeature regulatory_region_variant - - - - - - rs6499835 16:56442762 G 267 NM_001144.5 Transcript intron_variant - - - - - - rs6499835 16:56442762 G ENSESTG00000002355 ENSESTT00000005905 Transcript intron_variant - - - - - - rs6499835 16:56442762 G ENSESTG00000002355 ENSESTT00000005876 Transcript intron_variant - - - - - - rs6499835 16:56442762 G ENSESTG00000002355 ENSESTT00000005903 Transcript intron_variant - - - - - - rs6499835 16:56442762 G ENSESTG00000002355 ENSESTT00000005911 Transcript intron_variant - - - - - - rs6499835 16:56442762 G CCDS10758.1 CCDS10758.1 Transcript intron_variant - - - - - - rs6499835 16:56442762 G ENSESTG00000002355 ENSESTT00000005915 Transcript intron_variant - - - - - - rs282227 16:56591857 T - - - intergenic_variant - - - - - - rs2018331 16:56659020 G - ENSR00001505444 RegulatoryFeature regulatory_region_variant - - - - - - rs2018331 16:56659020 G ENSESTG00000029111 ENSESTT00000073350 Transcript upstream_gene_variant - - - - - - DISTANCE=676 rs2018331 16:56659020 G CCDS10764.2 CCDS10764.2 Transcript upstream_gene_variant - - - - - - DISTANCE=744 rs2018331 16:56659020 G ENSESTG00000029111 ENSESTT00000073328 Transcript intron_variant - - - - - - rs2018331 16:56659020 G ENSESTG00000029111 ENSESTT00000073385 Transcript upstream_gene_variant - - - - - - DISTANCE=727 rs2018331 16:56659020 G ENSESTG00000029111 ENSESTT00000073292 Transcript intron_variant - - - - - - rs2018331 16:56659020 G 4493 NM_175617.3 Transcript upstream_gene_variant - - - - - - DISTANCE=565 rs2018331 16:56659020 G ENSESTG00000029111 ENSESTT00000073306 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009835 Transcript downstream_gene_variant - - - - - - DISTANCE=214 rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009832 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009770 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009840 Transcript downstream_gene_variant - - - - - - DISTANCE=103 rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009752 Transcript intron_variant - - - - - - rs40185 16:58540595 G CCDS58467.1 CCDS58467.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009806 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009780 Transcript intron_variant - - - - - - rs40185 16:58540595 G 65009 NM_020465.3 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009767 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009764 Transcript intron_variant - - - - - - rs40185 16:58540595 G CCDS58465.1 CCDS58465.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G 65009 NM_022910.3 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009684 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009843 Transcript upstream_gene_variant - - - - - - DISTANCE=289 rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009706 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009823 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009817 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009787 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009829 Transcript intron_variant - - - - - - rs40185 16:58540595 G CCDS45500.1 CCDS45500.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G 65009 NM_001242836.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009828 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009756 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009689 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009825 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009814 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009718 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009796 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009804 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009704 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009674 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009751 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009779 Transcript intron_variant - - - - - - rs40185 16:58540595 G 65009 NM_001242834.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009748 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009795 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009826 Transcript intron_variant - - - - - - rs40185 16:58540595 G CCDS10797.1 CCDS10797.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009791 Transcript intron_variant - - - - - - rs40185 16:58540595 G CCDS58466.1 CCDS58466.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G CCDS55999.1 CCDS55999.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G 65009 NM_001242833.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009810 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009801 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009789 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009766 Transcript intron_variant - - - - - - rs40185 16:58540595 G 65009 NM_001242835.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009715 Transcript intron_variant - - - - - - rs40185 16:58540595 G 65009 NM_001130487.1 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009675 Transcript intron_variant - - - - - - rs40185 16:58540595 G 65009 NR_040072.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009842 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009822 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009700 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009800 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009830 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009702 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009712 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009820 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009794 Transcript intron_variant - - - - - - rs40185 16:58540595 G ENSESTG00000003820 ENSESTT00000009703 Transcript intron_variant - - - - - - rs4784990 16:58878583 T ENSESTG00000025314 ENSESTT00000063861 Transcript intron_variant - - - - - - rs4784990 16:58878583 T ENSESTG00000025324 ENSESTT00000063868 Transcript downstream_gene_variant - - - - - - DISTANCE=3129 rs1600255 16:58918943 C ENSESTG00000025324 ENSESTT00000063868 Transcript upstream_gene_variant - - - - - - DISTANCE=4992 rs42444 16:59429175 G - - - intergenic_variant - - - - - - rs34841 16:59431482 G - - - intergenic_variant - - - - - - rs2406660 16:59494566 T - - - intergenic_variant - - - - - - rs6500065 16:59839013 A - - - intergenic_variant - - - - - - rs216911 16:60314756 A - - - intergenic_variant - - - - - - rs1030255 16:60694120 C - - - intergenic_variant - - - - - - rs1424272 16:60895866 A - - - intergenic_variant - - - - - - rs8049836 16:61115018 A - - - intergenic_variant - - - - - - rs7193203 16:61271624 G - - - intergenic_variant - - - - - - rs9932367 16:61470153 C - - - intergenic_variant - - - - - - rs4331356 16:62597345 A - - - intergenic_variant - - - - - - rs6498913 16:63678907 C - - - intergenic_variant - - - - - - rs322584 16:63926608 A - - - intergenic_variant - - - - - - rs1381104 16:63975196 G - - - intergenic_variant - - - - - - rs4462614 16:64650481 T - - - intergenic_variant - - - - - - rs4408546 16:65603208 G 283867 NR_027755.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7405274 16:66380421 C - - - intergenic_variant - - - - - - rs27860 16:67324957 C CCDS45512.1 CCDS45512.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2246 rs27860 16:67324957 C ENSESTG00000021978 ENSESTT00000055514 Transcript downstream_gene_variant - - - - - - DISTANCE=1579 rs27860 16:67324957 C CCDS42179.1 CCDS42179.1 Transcript intron_variant - - - - - - rs27860 16:67324957 C 25894 NM_001129728.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs27860 16:67324957 C CCDS32466.1 CCDS32466.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2246 rs27860 16:67324957 C 146212 NM_001100915.1 Transcript intron_variant - - - - - - rs27860 16:67324957 C 25894 NM_001129727.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs27860 16:67324957 C 25894 NM_001129729.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs27860 16:67324957 C ENSESTG00000021978 ENSESTT00000055579 Transcript downstream_gene_variant - - - - - - DISTANCE=1579 rs27860 16:67324957 C 25894 NM_015432.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs27860 16:67324957 C ENSESTG00000021978 ENSESTT00000055573 Transcript downstream_gene_variant - - - - - - DISTANCE=1579 rs27860 16:67324957 C ENSESTG00000021978 ENSESTT00000055555 Transcript downstream_gene_variant - - - - - - DISTANCE=1579 rs27860 16:67324957 C 25894 NM_001129731.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs255051 16:68025801 C ENSESTG00000022011 ENSESTT00000055532 Transcript downstream_gene_variant - - - - - - DISTANCE=275 rs255051 16:68025801 C 64174 NM_022355.3 Transcript missense_variant 791 602 201 P/R cCt/cGt - PolyPhen=benign;SIFT=tolerated rs255051 16:68025801 C ENSESTG00000022011 ENSESTT00000055498 Transcript intron_variant - - - - - - rs255051 16:68025801 C ENSESTG00000020786 ENSESTT00000052361 Transcript upstream_gene_variant - - - - - - DISTANCE=2888 rs255051 16:68025801 C ENSESTG00000020786 ENSESTT00000052171 Transcript intron_variant - - - - - - rs255051 16:68025801 C ENSESTG00000022011 ENSESTT00000055487 Transcript downstream_gene_variant - - - - - - DISTANCE=919 rs255051 16:68025801 C ENSESTG00000022011 ENSESTT00000055565 Transcript missense_variant 758 602 201 P/R cCt/cGt - PolyPhen=benign;SIFT=tolerated rs255051 16:68025801 C ENSESTG00000020786 ENSESTT00000052131 Transcript intron_variant - - - - - - rs255051 16:68025801 C ENSESTG00000022011 ENSESTT00000055546 Transcript missense_variant 350 254 85 P/R cCt/cGt - rs255051 16:68025801 C ENSESTG00000022011 ENSESTT00000055476 Transcript missense_variant 654 128 43 P/R cCt/cGt - rs255051 16:68025801 C CCDS10857.1 CCDS10857.1 Transcript missense_variant 602 602 201 P/R cCt/cGt - PolyPhen=benign;SIFT=tolerated rs4783551 16:68177522 C 4775 NM_004555.3 Transcript intron_variant - - - - - - rs4783551 16:68177522 C ENSESTG00000021130 ENSESTT00000053204 Transcript downstream_gene_variant - - - - - - DISTANCE=4838 rs4783551 16:68177522 C ENSESTG00000021130 ENSESTT00000053147 Transcript intron_variant - - - - - - rs4783551 16:68177522 C ENSESTG00000021130 ENSESTT00000053201 Transcript intron_variant - - - - - - rs4783551 16:68177522 C ENSESTG00000021130 ENSESTT00000053228 Transcript downstream_gene_variant - - - - - - DISTANCE=4838 rs4783551 16:68177522 C ENSESTG00000021130 ENSESTT00000053189 Transcript intron_variant - - - - - - rs4783551 16:68177522 C 4775 NM_173163.2 Transcript intron_variant - - - - - - rs4783551 16:68177522 C ENSESTG00000021130 ENSESTT00000053222 Transcript intron_variant - - - - - - rs4783551 16:68177522 C ENSESTG00000021130 ENSESTT00000053157 Transcript downstream_gene_variant - - - - - - DISTANCE=4838 rs4783551 16:68177522 C CCDS10860.1 CCDS10860.1 Transcript intron_variant - - - - - - rs4783551 16:68177522 C CCDS10862.1 CCDS10862.1 Transcript intron_variant - - - - - - rs4783551 16:68177522 C 4775 NM_173165.2 Transcript intron_variant - - - - - - rs4783551 16:68177522 C CCDS10861.1 CCDS10861.1 Transcript intron_variant - - - - - - rs56156645 16:68876681 A CCDS45516.1 CCDS45516.1 Transcript upstream_gene_variant - - - - - - DISTANCE=840 rs56156645 16:68876681 A ENSESTG00000009150 ENSESTT00000022969 Transcript upstream_gene_variant - - - - - - DISTANCE=769 rs56156645 16:68876681 A ENSESTG00000009150 ENSESTT00000022977 Transcript upstream_gene_variant - - - - - - DISTANCE=769 rs56156645 16:68876681 A ENSESTG00000009150 ENSESTT00000022968 Transcript upstream_gene_variant - - - - - - DISTANCE=769 rs56156645 16:68876681 A 79613 NM_024562.1 Transcript upstream_gene_variant - - - - - - DISTANCE=828 rs56156645 16:68876681 A ENSESTG00000009150 ENSESTT00000022972 Transcript upstream_gene_variant - - - - - - DISTANCE=769 rs2965750 16:69764748 C ENSESTG00000018076 ENSESTT00000045611 Transcript upstream_gene_variant - - - - - - DISTANCE=4285 rs2965750 16:69764748 C CCDS32471.1 CCDS32471.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4406 rs2965750 16:69764748 C CCDS32472.1 CCDS32472.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4406 rs2965750 16:69764748 C CCDS10883.1 CCDS10883.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4406 rs2965750 16:69764748 C 1728 NM_001025433.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4215 rs2965750 16:69764748 C 1728 NM_001025434.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4215 rs2965750 16:69764748 C ENSESTG00000016266 ENSESTT00000040836 Transcript intron_variant - - - - - - rs2965750 16:69764748 C 1728 NM_000903.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4215 rs7205236 16:70758902 C - ENSR00000273008 RegulatoryFeature regulatory_region_variant - - - - - - rs7205236 16:70758902 C ENSESTG00000034874 ENSESTT00000088174 Transcript intron_variant - - - - - - rs7205236 16:70758902 C ENSESTG00000034807 ENSESTT00000087990 Transcript intron_variant - - - - - - rs7205236 16:70758902 C CCDS10896.1 CCDS10896.1 Transcript intron_variant - - - - - - rs7205236 16:70758902 C 55697 NM_018052.3 Transcript intron_variant - - - - - - rs7205236 16:70758902 C ENSESTG00000034874 ENSESTT00000088191 Transcript intron_variant - - - - - - rs7205236 16:70758902 C ENSESTG00000034874 ENSESTT00000088210 Transcript intron_variant - - - - - - rs4985365 16:70806729 C - ENSR00000273012 RegulatoryFeature regulatory_region_variant - - - - - - rs4985365 16:70806729 C ENSESTG00000034874 ENSESTT00000088181 Transcript intron_variant - - - - - - rs4985365 16:70806729 C ENSESTG00000034874 ENSESTT00000088174 Transcript intron_variant - - - - - - rs4985365 16:70806729 C ENSESTG00000034807 ENSESTT00000087990 Transcript intron_variant - - - - - - rs4985365 16:70806729 C CCDS10896.1 CCDS10896.1 Transcript intron_variant - - - - - - rs4985365 16:70806729 C 55697 NM_018052.3 Transcript intron_variant - - - - - - rs4985365 16:70806729 C 100130894 NR_034083.1 Transcript non_coding_exon_variant,nc_transcript_variant 1802 - - - - - rs4985365 16:70806729 C ENSESTG00000034874 ENSESTT00000088176 Transcript intron_variant - - - - - - rs3096376 16:71272827 A - - - intergenic_variant - - - - - - rs7188926 16:71379135 C - - - intergenic_variant - - - - - - rs4788798 16:71414914 C 794 NM_001740.4 Transcript intron_variant - - - - - - rs4788798 16:71414914 C 794 NR_027910.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs4788798 16:71414914 C 794 NM_007088.3 Transcript intron_variant - - - - - - rs4788798 16:71414914 C CCDS10899.1 CCDS10899.1 Transcript intron_variant - - - - - - rs4788798 16:71414914 C ENSESTG00000034827 ENSESTT00000088035 Transcript upstream_gene_variant - - - - - - DISTANCE=3766 rs9925241 16:71635533 G - - - intergenic_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090157 Transcript intron_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090159 Transcript intron_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090152 Transcript intron_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035697 ENSESTT00000090178 Transcript downstream_gene_variant - - - - - - DISTANCE=1887 rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090156 Transcript intron_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090154 Transcript downstream_gene_variant - - - - - - DISTANCE=4668 rs11075914 16:72050885 C 1723 NM_001361.4 Transcript intron_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090149 Transcript intron_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090150 Transcript intron_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090153 Transcript downstream_gene_variant - - - - - - DISTANCE=4718 rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090155 Transcript intron_variant - - - - - - rs11075914 16:72050885 C CCDS42192.1 CCDS42192.1 Transcript intron_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090158 Transcript intron_variant - - - - - - rs11075914 16:72050885 C ENSESTG00000035689 ENSESTT00000090151 Transcript intron_variant - - - - - - rs217174 16:72155795 T CCDS32483.1 CCDS32483.1 Transcript intron_variant - - - - - - rs217174 16:72155795 T 83449 NM_001160213.1 Transcript intron_variant - - - - - - rs217174 16:72155795 T 83449 NM_031293.2 Transcript intron_variant - - - - - - rs217174 16:72155795 T ENSESTG00000035696 ENSESTT00000090176 Transcript intron_variant - - - - - - rs217175 16:72155818 T CCDS32483.1 CCDS32483.1 Transcript intron_variant - - - - - - rs217175 16:72155818 T 83449 NM_001160213.1 Transcript intron_variant - - - - - - rs217175 16:72155818 T 83449 NM_031293.2 Transcript intron_variant - - - - - - rs217175 16:72155818 T ENSESTG00000035696 ENSESTT00000090176 Transcript intron_variant - - - - - - rs9302641 16:72695530 C ENSESTG00000002129 ENSESTT00000005232 Transcript intron_variant - - - - - - rs200267 16:74203431 A ENSESTG00000005197 ENSESTT00000013200 Transcript intron_variant - - - - - - rs2387391 16:74356355 C ENSESTG00000005191 ENSESTT00000013186 Transcript intron_variant - - - - - - rs7404788 16:74742179 T 79152 NM_024306.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4674 rs241383 16:74812186 C CCDS10911.1 CCDS10911.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3533 rs241383 16:74812186 C ENSESTG00000031915 ENSESTT00000080581 Transcript upstream_gene_variant - - - - - - DISTANCE=3457 rs241383 16:74812186 C 79152 NM_024306.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3457 rs12926049 16:74902607 T - ENSR00000510043 RegulatoryFeature regulatory_region_variant - - - - - - rs12926049 16:74902607 T 79726 NM_030581.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4864 rs11644597 16:75273330 G 9564 NM_001170715.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G 9564 NM_001170717.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G CCDS54043.1 CCDS54043.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079848 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079906 Transcript intron_variant - - - - - - rs11644597 16:75273330 G 9564 NM_001170714.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G 9564 NM_014567.3 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079934 Transcript downstream_gene_variant - - - - - - DISTANCE=3344 rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079909 Transcript intron_variant - - - - - - rs11644597 16:75273330 G CCDS54042.1 CCDS54042.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079889 Transcript intron_variant - - - - - - rs11644597 16:75273330 G 9564 NM_001170716.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079947 Transcript downstream_gene_variant - - - - - - DISTANCE=3623 rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079874 Transcript downstream_gene_variant - - - - - - DISTANCE=3558 rs11644597 16:75273330 G CCDS54039.1 CCDS54039.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079927 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079866 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079956 Transcript downstream_gene_variant - - - - - - DISTANCE=3433 rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079919 Transcript intron_variant - - - - - - rs11644597 16:75273330 G CCDS54038.1 CCDS54038.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G CCDS54040.1 CCDS54040.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G 9564 NM_001170718.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G CCDS54037.1 CCDS54037.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079965 Transcript intron_variant - - - - - - rs11644597 16:75273330 G 9564 NM_001170719.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G CCDS54041.1 CCDS54041.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G 9564 NM_001170720.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G 9564 NM_001170721.1 Transcript upstream_gene_variant - - - - - - DISTANCE=350 rs11644597 16:75273330 G CCDS10915.1 CCDS10915.1 Transcript intron_variant - - - - - - rs11644597 16:75273330 G ENSESTG00000031629 ENSESTT00000079897 Transcript downstream_gene_variant - - - - - - DISTANCE=3553 rs12716786 16:75367413 T CCDS10916.1 CCDS10916.1 Transcript intron_variant - - - - - - rs12716786 16:75367413 T 10428 NM_006324.2 Transcript intron_variant - - - - - - rs1166205 16:75589080 A - ENSR00000149521 RegulatoryFeature regulatory_region_variant - - - - - - rs1166205 16:75589080 A 79583 NM_001077416.1 Transcript intron_variant - - - - - - rs1166205 16:75589080 A ENSESTG00000000192 ENSESTT00000000502 Transcript intron_variant - - - - - - rs1166205 16:75589080 A ENSESTG00000000192 ENSESTT00000000507 Transcript intron_variant - - - - - - rs1166205 16:75589080 A 79583 NM_001077418.1 Transcript intron_variant - - - - - - rs1166205 16:75589080 A CCDS45531.1 CCDS45531.1 Transcript intron_variant - - - - - - rs1166205 16:75589080 A ENSESTG00000000192 ENSESTT00000000498 Transcript intron_variant - - - - - - rs1166205 16:75589080 A ENSESTG00000000192 ENSESTT00000000505 Transcript intron_variant - - - - - - rs1166205 16:75589080 A ENSESTG00000000192 ENSESTT00000000475 Transcript intron_variant - - - - - - rs1166205 16:75589080 A CCDS45530.1 CCDS45530.1 Transcript intron_variant - - - - - - rs1166205 16:75589080 A 79583 NM_001077419.1 Transcript intron_variant - - - - - - rs8047430 16:75678984 T CCDS32491.1 CCDS32491.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2797 rs8047430 16:75678984 T ENSESTG00000000155 ENSESTT00000000405 Transcript intron_variant - - - - - - rs8047430 16:75678984 T 54386 NM_018975.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2651 rs8047430 16:75678984 T 3735 NM_001130089.1 Transcript intron_variant - - - - - - rs8047430 16:75678984 T CCDS45532.1 CCDS45532.1 Transcript upstream_gene_variant - - - - - - DISTANCE=658 rs8047430 16:75678984 T 3735 NM_005548.2 Transcript intron_variant - - - - - - rs8047430 16:75678984 T ENSESTG00000000155 ENSESTT00000000410 Transcript intron_variant - - - - - - rs8047430 16:75678984 T ENSESTG00000000155 ENSESTT00000000404 Transcript intron_variant - - - - - - rs8047430 16:75678984 T CCDS10923.1 CCDS10923.1 Transcript intron_variant - - - - - - rs8047430 16:75678984 T ENSESTG00000000155 ENSESTT00000000403 Transcript intron_variant - - - - - - rs1165946 16:75716208 T - ENSR00000510223 RegulatoryFeature regulatory_region_variant - - - - - - rs1165946 16:75716208 T - - - intergenic_variant - - - - - - rs6564280 16:75782464 G - - - intergenic_variant - - - - - - rs6564286 16:75818297 C - - - intergenic_variant - - - - - - rs1030265 16:75845760 G - - - intergenic_variant - - - - - - rs4476201 16:75875270 G - - - intergenic_variant - - - - - - rs2133053 16:76038973 C - - - intergenic_variant - - - - - - rs6564328 16:76436439 G 85445 NM_033401.3 Transcript intron_variant - - - - - - rs6564328 16:76436439 G ENSESTG00000000140 ENSESTT00000000371 Transcript intron_variant - - - - - - rs6564328 16:76436439 G CCDS10924.2 CCDS10924.2 Transcript intron_variant - - - - - - rs6564328 16:76436439 G 85445 NM_138994.3 Transcript intron_variant - - - - - - rs6564352 16:76635422 A - - - intergenic_variant - - - - - - rs6564375 16:76905742 C ENSESTG00000005590 ENSESTT00000014216 Transcript intron_variant - - - - - - rs6564375 16:76905742 C 100616172 NR_039870.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2826 rs677902 16:77037997 A - - - intergenic_variant - - - - - - rs284932 16:77066221 A - - - intergenic_variant - - - - - - rs1549665 16:77374454 G ENSESTG00000005665 ENSESTT00000014396 Transcript intron_variant - - - - - - rs1549665 16:77374454 G CCDS10926.1 CCDS10926.1 Transcript intron_variant - - - - - - rs1549665 16:77374454 G 170692 NM_199355.2 Transcript intron_variant - - - - - - rs1549665 16:77374454 G ENSESTG00000005665 ENSESTT00000014392 Transcript intron_variant - - - - - - rs387678 16:77621754 A - - - intergenic_variant - - - - - - rs435052 16:77665677 T - - - intergenic_variant - - - - - - rs8057309 16:77706493 A - - - intergenic_variant - - - - - - rs4887916 16:77716784 G - - - intergenic_variant - - - - - - rs1900892 16:77736683 C - - - intergenic_variant - - - - - - rs254774 16:77882515 A CCDS32492.1 CCDS32492.1 Transcript intron_variant - - - - - - rs254774 16:77882515 A 57687 NM_020927.1 Transcript intron_variant - - - - - - rs254774 16:77882515 A ENSESTG00000000975 ENSESTT00000002358 Transcript intron_variant - - - - - - rs254774 16:77882515 A ENSESTG00000001103 ENSESTT00000002631 Transcript intron_variant - - - - - - rs443802 16:77955215 C CCDS32492.1 CCDS32492.1 Transcript intron_variant - - - - - - rs443802 16:77955215 C 57687 NM_020927.1 Transcript intron_variant - - - - - - rs443802 16:77955215 C ENSESTG00000000975 ENSESTT00000002358 Transcript intron_variant - - - - - - rs443802 16:77955215 C ENSESTG00000001094 ENSESTT00000002614 Transcript intron_variant - - - - - - rs443802 16:77955215 C ENSESTG00000001103 ENSESTT00000002631 Transcript intron_variant - - - - - - rs1677302 16:77976386 G CCDS32492.1 CCDS32492.1 Transcript intron_variant - - - - - - rs1677302 16:77976386 G 57687 NM_020927.1 Transcript intron_variant - - - - - - rs1677302 16:77976386 G ENSESTG00000000975 ENSESTT00000002358 Transcript intron_variant - - - - - - rs1677302 16:77976386 G ENSESTG00000001094 ENSESTT00000002614 Transcript intron_variant - - - - - - rs429467 16:77993789 C CCDS32492.1 CCDS32492.1 Transcript intron_variant - - - - - - rs429467 16:77993789 C 57687 NM_020927.1 Transcript intron_variant - - - - - - rs429467 16:77993789 C ENSESTG00000000975 ENSESTT00000002358 Transcript intron_variant - - - - - - rs429467 16:77993789 C ENSESTG00000001094 ENSESTT00000002614 Transcript intron_variant - - - - - - rs366434 16:78005216 C CCDS32492.1 CCDS32492.1 Transcript intron_variant - - - - - - rs366434 16:78005216 C 57687 NM_020927.1 Transcript intron_variant - - - - - - rs366434 16:78005216 C ENSESTG00000000975 ENSESTT00000002358 Transcript intron_variant - - - - - - rs366434 16:78005216 C ENSESTG00000001094 ENSESTT00000002614 Transcript intron_variant - - - - - - rs392432 16:78007487 C CCDS32492.1 CCDS32492.1 Transcript intron_variant - - - - - - rs392432 16:78007487 C ENSESTG00000001096 ENSESTT00000002626 Transcript downstream_gene_variant - - - - - - DISTANCE=4801 rs392432 16:78007487 C 57687 NM_020927.1 Transcript intron_variant - - - - - - rs392432 16:78007487 C ENSESTG00000000975 ENSESTT00000002358 Transcript intron_variant - - - - - - rs392432 16:78007487 C ENSESTG00000001094 ENSESTT00000002614 Transcript intron_variant - - - - - - rs1171862 16:78036077 A ENSESTG00000001094 ENSESTT00000002614 Transcript intron_variant - - - - - - rs1171863 16:78038728 C ENSESTG00000001094 ENSESTT00000002614 Transcript intron_variant - - - - - - rs7198650 16:78293061 A ENSESTG00000001025 ENSESTT00000002480 Transcript intron_variant - - - - - - rs7198650 16:78293061 A CCDS42196.1 CCDS42196.1 Transcript intron_variant - - - - - - rs7198650 16:78293061 A 51741 NM_130791.2 Transcript intron_variant - - - - - - rs7198650 16:78293061 A CCDS42197.1 CCDS42197.1 Transcript intron_variant - - - - - - rs7198650 16:78293061 A 51741 NM_016373.2 Transcript intron_variant - - - - - - rs7198650 16:78293061 A ENSESTG00000001090 ENSESTT00000002608 Transcript downstream_gene_variant - - - - - - DISTANCE=1481 rs2458028 16:78588397 T CCDS42196.1 CCDS42196.1 Transcript intron_variant - - - - - - rs2458028 16:78588397 T ENSESTG00000023327 ENSESTT00000058851 Transcript upstream_gene_variant - - - - - - DISTANCE=4668 rs2458028 16:78588397 T 51741 NM_016373.2 Transcript intron_variant - - - - - - rs2458028 16:78588397 T ENSESTG00000023317 ENSESTT00000058836 Transcript intron_variant - - - - - - rs1110555 16:78734120 A CCDS42196.1 CCDS42196.1 Transcript intron_variant - - - - - - rs1110555 16:78734120 A 51741 NM_016373.2 Transcript intron_variant - - - - - - rs1110555 16:78734120 A ENSESTG00000023308 ENSESTT00000058813 Transcript intron_variant - - - - - - rs2656627 16:78912101 G CCDS42196.1 CCDS42196.1 Transcript intron_variant - - - - - - rs2656627 16:78912101 G 51741 NM_016373.2 Transcript intron_variant - - - - - - rs2346817 16:78957640 G CCDS42196.1 CCDS42196.1 Transcript intron_variant - - - - - - rs2346817 16:78957640 G 51741 NM_016373.2 Transcript intron_variant - - - - - - rs2550726 16:79047344 C - ENSR00000665919 RegulatoryFeature regulatory_region_variant - - - - - - rs2550726 16:79047344 C CCDS42196.1 CCDS42196.1 Transcript intron_variant - - - - - - rs2550726 16:79047344 C 51741 NM_016373.2 Transcript intron_variant - - - - - - rs11642382 16:79377079 A - - - intergenic_variant - - - - - - rs2549506 16:79539499 C - - - intergenic_variant - - - - - - rs2549507 16:79547364 T - - - intergenic_variant - - - - - - rs2045929 16:80217291 A ENSESTG00000025854 ENSESTT00000065152 Transcript downstream_gene_variant - - - - - - DISTANCE=2712 rs1564221 16:80237502 A - - - intergenic_variant - - - - - - rs4393585 16:80496833 G - ENSR00001506812 RegulatoryFeature regulatory_region_variant - - - - - - rs4393585 16:80496833 G - - - intergenic_variant - - - - - - rs7186611 16:80576130 G 83657 NM_130897.1 Transcript intron_variant - - - - - - rs7186611 16:80576130 G CCDS10929.1 CCDS10929.1 Transcript intron_variant - - - - - - rs7186611 16:80576130 G ENSESTG00000003660 ENSESTT00000009176 Transcript intron_variant - - - - - - rs12445721 16:80580055 A 83657 NM_130897.1 Transcript intron_variant - - - - - - rs12445721 16:80580055 A CCDS10929.1 CCDS10929.1 Transcript intron_variant - - - - - - rs12445721 16:80580055 A ENSESTG00000003660 ENSESTT00000009176 Transcript intron_variant - - - - - - rs12716892 16:80661990 A 124359 NM_152342.2 Transcript intron_variant - - - - - - rs12716892 16:80661990 A CCDS32493.1 CCDS32493.1 Transcript intron_variant - - - - - - rs2549737 16:80789098 C 124359 NM_152342.2 Transcript intron_variant - - - - - - rs2549737 16:80789098 C ENSESTG00000003793 ENSESTT00000009560 Transcript intron_variant - - - - - - rs2549737 16:80789098 C CCDS32493.1 CCDS32493.1 Transcript intron_variant - - - - - - rs2549820 16:81014324 C CCDS10930.1 CCDS10930.1 Transcript intron_variant - - - - - - rs2549820 16:81014324 C ENSESTG00000003665 ENSESTT00000009187 Transcript intron_variant - - - - - - rs2549820 16:81014324 C 56942 NM_020188.3 Transcript intron_variant - - - - - - rs2549820 16:81014324 C ENSESTG00000003781 ENSESTT00000009520 Transcript intron_variant - - - - - - rs2549820 16:81014324 C ENSESTG00000003781 ENSESTT00000009529 Transcript intron_variant - - - - - - rs6564829 16:81218455 C 114780 NM_052892.3 Transcript intron_variant - - - - - - rs6564829 16:81218455 C CCDS42202.1 CCDS42202.1 Transcript intron_variant - - - - - - rs6564829 16:81218455 C 114780 NM_001076780.1 Transcript intron_variant - - - - - - rs2927308 16:81536691 T ENSESTG00000020071 ENSESTT00000050319 Transcript intron_variant - - - - - - rs2927308 16:81536691 T CCDS54044.1 CCDS54044.1 Transcript intron_variant - - - - - - rs2927308 16:81536691 T 80790 NM_198390.2 Transcript intron_variant - - - - - - rs2927308 16:81536691 T CCDS54045.1 CCDS54045.1 Transcript intron_variant - - - - - - rs2927308 16:81536691 T 80790 NM_030629.2 Transcript intron_variant - - - - - - rs7194787 16:81865196 G - ENSR00001035623 RegulatoryFeature regulatory_region_variant - - - - - - rs7194787 16:81865196 G ENSESTG00000020334 ENSESTT00000051210 Transcript intron_variant - - - - - - rs7194787 16:81865196 G ENSESTG00000020334 ENSESTT00000051058 Transcript intron_variant - - - - - - rs7194787 16:81865196 G ENSESTG00000020334 ENSESTT00000051231 Transcript intron_variant - - - - - - rs7194787 16:81865196 G ENSESTG00000020334 ENSESTT00000051165 Transcript intron_variant - - - - - - rs7194787 16:81865196 G 5336 NM_002661.3 Transcript intron_variant - - - - - - rs7194787 16:81865196 G ENSESTG00000020334 ENSESTT00000051134 Transcript intron_variant - - - - - - rs7194787 16:81865196 G ENSESTG00000020334 ENSESTT00000051092 Transcript intron_variant - - - - - - rs7194787 16:81865196 G ENSESTG00000020334 ENSESTT00000051178 Transcript intron_variant - - - - - - rs7194787 16:81865196 G ENSESTG00000020334 ENSESTT00000051226 Transcript intron_variant - - - - - - rs7194787 16:81865196 G CCDS42204.1 CCDS42204.1 Transcript intron_variant - - - - - - rs7194787 16:81865196 G ENSESTG00000020334 ENSESTT00000051196 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051264 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051210 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051058 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051231 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051165 Transcript intron_variant - - - - - - rs7198768 16:81890471 T 5336 NM_002661.3 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051134 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051092 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051178 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051226 Transcript intron_variant - - - - - - rs7198768 16:81890471 T CCDS42204.1 CCDS42204.1 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051253 Transcript intron_variant - - - - - - rs7198768 16:81890471 T ENSESTG00000020334 ENSESTT00000051196 Transcript intron_variant - - - - - - rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051264 Transcript downstream_gene_variant - - - - - - DISTANCE=2685 rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051210 Transcript downstream_gene_variant - - - - - - DISTANCE=2685 rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051058 Transcript intron_variant - - - - - - rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051231 Transcript downstream_gene_variant - - - - - - DISTANCE=2685 rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051165 Transcript downstream_gene_variant - - - - - - DISTANCE=2685 rs4563037 16:81936976 G 5336 NM_002661.3 Transcript intron_variant - - - - - - rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051134 Transcript intron_variant - - - - - - rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051551 Transcript intron_variant - - - - - - rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051092 Transcript downstream_gene_variant - - - - - - DISTANCE=2685 rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051178 Transcript downstream_gene_variant - - - - - - DISTANCE=2685 rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051226 Transcript intron_variant - - - - - - rs4563037 16:81936976 G CCDS42204.1 CCDS42204.1 Transcript intron_variant - - - - - - rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051562 Transcript intron_variant - - - - - - rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051253 Transcript intron_variant - - - - - - rs4563037 16:81936976 G ENSESTG00000020334 ENSESTT00000051196 Transcript intron_variant - - - - - - rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051264 Transcript downstream_gene_variant - - - - - - DISTANCE=3676 rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051210 Transcript downstream_gene_variant - - - - - - DISTANCE=3676 rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051058 Transcript intron_variant - - - - - - rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051231 Transcript downstream_gene_variant - - - - - - DISTANCE=3676 rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051165 Transcript downstream_gene_variant - - - - - - DISTANCE=3676 rs4482276 16:81937967 C 5336 NM_002661.3 Transcript intron_variant - - - - - - rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051134 Transcript intron_variant - - - - - - rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051551 Transcript intron_variant - - - - - - rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051092 Transcript downstream_gene_variant - - - - - - DISTANCE=3676 rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051178 Transcript downstream_gene_variant - - - - - - DISTANCE=3676 rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051226 Transcript intron_variant - - - - - - rs4482276 16:81937967 C CCDS42204.1 CCDS42204.1 Transcript intron_variant - - - - - - rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051562 Transcript intron_variant - - - - - - rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051253 Transcript intron_variant - - - - - - rs4482276 16:81937967 C ENSESTG00000020334 ENSESTT00000051196 Transcript intron_variant - - - - - - rs4889439 16:81948136 C 5336 NM_002661.3 Transcript intron_variant - - - - - - rs4889439 16:81948136 C ENSESTG00000020334 ENSESTT00000051551 Transcript intron_variant - - - - - - rs4889439 16:81948136 C CCDS42204.1 CCDS42204.1 Transcript intron_variant - - - - - - rs4889439 16:81948136 C ENSESTG00000020334 ENSESTT00000051562 Transcript downstream_gene_variant - - - - - - DISTANCE=1814 rs12448152 16:81953368 G 5336 NM_002661.3 Transcript intron_variant - - - - - - rs12448152 16:81953368 G ENSESTG00000020334 ENSESTT00000051551 Transcript intron_variant - - - - - - rs12448152 16:81953368 G CCDS42204.1 CCDS42204.1 Transcript intron_variant - - - - - - rs11150433 16:82065725 G - ENSR00000510885 RegulatoryFeature regulatory_region_variant - - - - - - rs11150433 16:82065725 G ENSESTG00000020826 ENSESTT00000052267 Transcript upstream_gene_variant - - - - - - DISTANCE=2884 rs11150433 16:82065725 G CCDS10936.1 CCDS10936.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3305 rs11150433 16:82065725 G 3294 NM_002153.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3133 rs11150433 16:82065725 G ENSESTG00000020826 ENSESTT00000052319 Transcript upstream_gene_variant - - - - - - DISTANCE=3223 rs2955154 16:82124776 T ENSESTG00000020826 ENSESTT00000052267 Transcript intron_variant - - - - - - rs2955154 16:82124776 T CCDS10936.1 CCDS10936.1 Transcript intron_variant - - - - - - rs2955154 16:82124776 T 3294 NM_002153.2 Transcript intron_variant - - - - - - rs2955154 16:82124776 T ENSESTG00000020826 ENSESTT00000052319 Transcript intron_variant - - - - - - rs2317851 16:82427177 T - - - intergenic_variant - - - - - - rs3843719 16:82446111 A - - - intergenic_variant - - - - - - rs889627 16:82493529 A - - - intergenic_variant - - - - - - rs1424058 16:82493597 G - - - intergenic_variant - - - - - - rs3848295 16:82550407 G - ENSR00001506938 RegulatoryFeature regulatory_region_variant - - - - - - rs3848295 16:82550407 G - - - intergenic_variant - - - - - - rs4782716 16:82609695 A - - - intergenic_variant - - - - - - rs9925095 16:82675969 C CCDS56009.1 CCDS56009.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C 1012 NM_001220492.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs9925095 16:82675969 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs9925095 16:82675969 C 1012 NM_001220491.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs9925095 16:82675969 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C CCDS56010.1 CCDS56010.1 Transcript intron_variant - - - - - - rs9925095 16:82675969 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs1559313 16:82951924 A CCDS56009.1 CCDS56009.1 Transcript intron_variant - - - - - - rs1559313 16:82951924 A ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs1559313 16:82951924 A 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs1559313 16:82951924 A 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs1559313 16:82951924 A 1012 NM_001220492.1 Transcript intron_variant - - - - - - rs1559313 16:82951924 A CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs1559313 16:82951924 A CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs1559313 16:82951924 A CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs1559313 16:82951924 A ENSESTG00000014477 ENSESTT00000036297 Transcript intron_variant - - - - - - rs1559313 16:82951924 A ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs1559313 16:82951924 A 1012 NM_001257.4 Transcript intron_variant - - - - - - rs1559313 16:82951924 A ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs1559313 16:82951924 A 1012 NM_001220491.1 Transcript intron_variant - - - - - - rs1559313 16:82951924 A ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs1559313 16:82951924 A 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs1559313 16:82951924 A ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs1559313 16:82951924 A CCDS56010.1 CCDS56010.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A - ENSR00000510966 RegulatoryFeature regulatory_region_variant - - - - - - rs7405246 16:82971871 A CCDS56009.1 CCDS56009.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs7405246 16:82971871 A 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A 1012 NM_001220492.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A ENSESTG00000014477 ENSESTT00000036297 Transcript intron_variant - - - - - - rs7405246 16:82971871 A ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs7405246 16:82971871 A 1012 NM_001257.4 Transcript intron_variant - - - - - - rs7405246 16:82971871 A ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs7405246 16:82971871 A 1012 NM_001220491.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs7405246 16:82971871 A 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs7405246 16:82971871 A ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs7405246 16:82971871 A CCDS56010.1 CCDS56010.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G CCDS56009.1 CCDS56009.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs6565094 16:83007198 G 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G 1012 NM_001220492.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G ENSESTG00000014477 ENSESTT00000036297 Transcript intron_variant - - - - - - rs6565094 16:83007198 G ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs6565094 16:83007198 G 1012 NM_001257.4 Transcript intron_variant - - - - - - rs6565094 16:83007198 G ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs6565094 16:83007198 G 1012 NM_001220491.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs6565094 16:83007198 G 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs6565094 16:83007198 G ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs6565094 16:83007198 G CCDS56010.1 CCDS56010.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A CCDS56009.1 CCDS56009.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs6565102 16:83053768 A 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A 1012 NM_001220492.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A ENSESTG00000014477 ENSESTT00000036297 Transcript intron_variant - - - - - - rs6565102 16:83053768 A ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs6565102 16:83053768 A 1012 NM_001257.4 Transcript intron_variant - - - - - - rs6565102 16:83053768 A ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs6565102 16:83053768 A 1012 NM_001220491.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs6565102 16:83053768 A 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs6565102 16:83053768 A ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs6565102 16:83053768 A CCDS56010.1 CCDS56010.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G CCDS56009.1 CCDS56009.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs10048107 16:83200518 G 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G 1012 NM_001220492.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G ENSESTG00000014477 ENSESTT00000036297 Transcript intron_variant - - - - - - rs10048107 16:83200518 G ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs10048107 16:83200518 G 1012 NM_001257.4 Transcript intron_variant - - - - - - rs10048107 16:83200518 G ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs10048107 16:83200518 G 1012 NM_001220491.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs10048107 16:83200518 G 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs10048107 16:83200518 G ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs10048107 16:83200518 G CCDS56010.1 CCDS56010.1 Transcript intron_variant - - - - - - rs2875756 16:83496825 G ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs2875756 16:83496825 G 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs2875756 16:83496825 G 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs2875756 16:83496825 G ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs2875756 16:83496825 G CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs2875756 16:83496825 G CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs2875756 16:83496825 G 1012 NM_001257.4 Transcript intron_variant - - - - - - rs2875756 16:83496825 G ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs2875756 16:83496825 G ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs2875756 16:83496825 G 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs2875756 16:83496825 G CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs2875756 16:83496825 G ENSESTG00000014477 ENSESTT00000036297 Transcript intron_variant - - - - - - rs2875756 16:83496825 G ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs902018 16:83500521 C ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs902018 16:83500521 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs902018 16:83500521 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs902018 16:83500521 C ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs902018 16:83500521 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs902018 16:83500521 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs902018 16:83500521 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs902018 16:83500521 C ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs902018 16:83500521 C ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs902018 16:83500521 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs902018 16:83500521 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs902018 16:83500521 C ENSESTG00000014477 ENSESTT00000036297 Transcript intron_variant - - - - - - rs902018 16:83500521 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs902021 16:83501086 C ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs902021 16:83501086 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs902021 16:83501086 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs902021 16:83501086 C ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs902021 16:83501086 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs902021 16:83501086 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs902021 16:83501086 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs902021 16:83501086 C ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs902021 16:83501086 C ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs902021 16:83501086 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs902021 16:83501086 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs902021 16:83501086 C ENSESTG00000014477 ENSESTT00000036297 Transcript intron_variant - - - - - - rs902021 16:83501086 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs923420 16:83515290 T ENSESTG00000005476 ENSESTT00000013967 Transcript upstream_gene_variant - - - - - - DISTANCE=4909 rs923420 16:83515290 T ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs923420 16:83515290 T 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs923420 16:83515290 T 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs923420 16:83515290 T ENSESTG00000014477 ENSESTT00000036285 Transcript intron_variant - - - - - - rs923420 16:83515290 T ENSESTG00000005476 ENSESTT00000013963 Transcript upstream_gene_variant - - - - - - DISTANCE=4800 rs923420 16:83515290 T CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs923420 16:83515290 T CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs923420 16:83515290 T 1012 NM_001257.4 Transcript intron_variant - - - - - - rs923420 16:83515290 T ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs923420 16:83515290 T ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs923420 16:83515290 T 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs923420 16:83515290 T CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs923420 16:83515290 T ENSESTG00000014477 ENSESTT00000036297 Transcript intron_variant - - - - - - rs923420 16:83515290 T ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs923418 16:83525388 C ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs923418 16:83525388 C ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs923418 16:83525388 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs923418 16:83525388 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs923418 16:83525388 C ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs923418 16:83525388 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs923418 16:83525388 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs923418 16:83525388 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs923418 16:83525388 C ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs923418 16:83525388 C ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs923418 16:83525388 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs923418 16:83525388 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs923418 16:83525388 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs4782802 16:83531886 C ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs4782802 16:83531886 C ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs4782802 16:83531886 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs4782802 16:83531886 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs4782802 16:83531886 C ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs4782802 16:83531886 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs4782802 16:83531886 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs4782802 16:83531886 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs4782802 16:83531886 C ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs4782802 16:83531886 C ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs4782802 16:83531886 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs4782802 16:83531886 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs4782802 16:83531886 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs6563919 16:83534612 G ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs6563919 16:83534612 G ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs6563919 16:83534612 G 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs6563919 16:83534612 G 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs6563919 16:83534612 G ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs6563919 16:83534612 G CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs6563919 16:83534612 G CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs6563919 16:83534612 G 1012 NM_001257.4 Transcript intron_variant - - - - - - rs6563919 16:83534612 G ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs6563919 16:83534612 G ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs6563919 16:83534612 G 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs6563919 16:83534612 G CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs6563919 16:83534612 G ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs6563920 16:83534675 G ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs6563920 16:83534675 G ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs6563920 16:83534675 G 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs6563920 16:83534675 G 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs6563920 16:83534675 G ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs6563920 16:83534675 G CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs6563920 16:83534675 G CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs6563920 16:83534675 G 1012 NM_001257.4 Transcript intron_variant - - - - - - rs6563920 16:83534675 G ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs6563920 16:83534675 G ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs6563920 16:83534675 G 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs6563920 16:83534675 G CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs6563920 16:83534675 G ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs4782538 16:83536666 G ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs4782538 16:83536666 G ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs4782538 16:83536666 G 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs4782538 16:83536666 G 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs4782538 16:83536666 G ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs4782538 16:83536666 G CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs4782538 16:83536666 G CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs4782538 16:83536666 G 1012 NM_001257.4 Transcript intron_variant - - - - - - rs4782538 16:83536666 G ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs4782538 16:83536666 G ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs4782538 16:83536666 G 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs4782538 16:83536666 G CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs4782538 16:83536666 G ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs4782804 16:83537306 G ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs4782804 16:83537306 G ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs4782804 16:83537306 G 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs4782804 16:83537306 G 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs4782804 16:83537306 G ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs4782804 16:83537306 G CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs4782804 16:83537306 G CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs4782804 16:83537306 G 100422853 NR_036147.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4645 rs4782804 16:83537306 G 1012 NM_001257.4 Transcript intron_variant - - - - - - rs4782804 16:83537306 G ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs4782804 16:83537306 G ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs4782804 16:83537306 G 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs4782804 16:83537306 G CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs4782804 16:83537306 G ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs4238690 16:83547309 A - ENSR00001507012 RegulatoryFeature regulatory_region_variant - - - - - - rs4238690 16:83547309 A ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs4238690 16:83547309 A ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs4238690 16:83547309 A 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs4238690 16:83547309 A 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs4238690 16:83547309 A ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs4238690 16:83547309 A CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs4238690 16:83547309 A CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs4238690 16:83547309 A 1012 NM_001257.4 Transcript intron_variant - - - - - - rs4238690 16:83547309 A ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs4238690 16:83547309 A ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs4238690 16:83547309 A 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs4238690 16:83547309 A CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs4238690 16:83547309 A ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs10468352 16:83551589 G ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs10468352 16:83551589 G ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs10468352 16:83551589 G 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs10468352 16:83551589 G 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs10468352 16:83551589 G ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs10468352 16:83551589 G CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs10468352 16:83551589 G CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs10468352 16:83551589 G 1012 NM_001257.4 Transcript intron_variant - - - - - - rs10468352 16:83551589 G ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs10468352 16:83551589 G ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs10468352 16:83551589 G 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs10468352 16:83551589 G CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs10468352 16:83551589 G ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs9921765 16:83565383 T ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs9921765 16:83565383 T ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs9921765 16:83565383 T 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs9921765 16:83565383 T 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs9921765 16:83565383 T ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs9921765 16:83565383 T CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs9921765 16:83565383 T CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs9921765 16:83565383 T 1012 NM_001257.4 Transcript intron_variant - - - - - - rs9921765 16:83565383 T ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs9921765 16:83565383 T ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs9921765 16:83565383 T 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs9921765 16:83565383 T CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs9921765 16:83565383 T ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs4457978 16:83577554 C ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs4457978 16:83577554 C ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs4457978 16:83577554 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs4457978 16:83577554 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs4457978 16:83577554 C ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs4457978 16:83577554 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs4457978 16:83577554 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs4457978 16:83577554 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs4457978 16:83577554 C ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs4457978 16:83577554 C ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs4457978 16:83577554 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs4457978 16:83577554 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs4457978 16:83577554 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs4558402 16:83586652 C ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs4558402 16:83586652 C ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs4558402 16:83586652 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs4558402 16:83586652 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs4558402 16:83586652 C ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs4558402 16:83586652 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs4558402 16:83586652 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs4558402 16:83586652 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs4558402 16:83586652 C ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs4558402 16:83586652 C ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs4558402 16:83586652 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs4558402 16:83586652 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs4558402 16:83586652 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs7189702 16:83593332 T ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs7189702 16:83593332 T ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs7189702 16:83593332 T 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs7189702 16:83593332 T 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs7189702 16:83593332 T ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs7189702 16:83593332 T CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs7189702 16:83593332 T CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs7189702 16:83593332 T 1012 NM_001257.4 Transcript intron_variant - - - - - - rs7189702 16:83593332 T ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs7189702 16:83593332 T ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs7189702 16:83593332 T 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs7189702 16:83593332 T CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs7189702 16:83593332 T ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs4511515 16:83595069 C ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs4511515 16:83595069 C ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs4511515 16:83595069 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs4511515 16:83595069 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs4511515 16:83595069 C ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs4511515 16:83595069 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs4511515 16:83595069 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs4511515 16:83595069 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs4511515 16:83595069 C ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs4511515 16:83595069 C ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs4511515 16:83595069 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs4511515 16:83595069 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs4511515 16:83595069 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs4782546 16:83603273 G ENSESTG00000005476 ENSESTT00000013967 Transcript intron_variant - - - - - - rs4782546 16:83603273 G ENSESTG00000014477 ENSESTT00000036296 Transcript intron_variant - - - - - - rs4782546 16:83603273 G 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs4782546 16:83603273 G 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs4782546 16:83603273 G ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs4782546 16:83603273 G CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs4782546 16:83603273 G CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs4782546 16:83603273 G 1012 NM_001257.4 Transcript intron_variant - - - - - - rs4782546 16:83603273 G ENSESTG00000014477 ENSESTT00000036278 Transcript intron_variant - - - - - - rs4782546 16:83603273 G ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs4782546 16:83603273 G 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs4782546 16:83603273 G CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs4782546 16:83603273 G ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs7193863 16:83659364 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs7193863 16:83659364 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs7193863 16:83659364 C ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs7193863 16:83659364 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs7193863 16:83659364 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs7193863 16:83659364 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs7193863 16:83659364 C ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs7193863 16:83659364 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs7193863 16:83659364 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs7193863 16:83659364 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs11866399 16:83683041 C 1012 NM_001220488.1 Transcript intron_variant - - - - - - rs11866399 16:83683041 C 1012 NM_001220489.1 Transcript intron_variant - - - - - - rs11866399 16:83683041 C ENSESTG00000005476 ENSESTT00000013963 Transcript intron_variant - - - - - - rs11866399 16:83683041 C CCDS58486.1 CCDS58486.1 Transcript intron_variant - - - - - - rs11866399 16:83683041 C CCDS58487.1 CCDS58487.1 Transcript intron_variant - - - - - - rs11866399 16:83683041 C 1012 NM_001257.4 Transcript intron_variant - - - - - - rs11866399 16:83683041 C ENSESTG00000014477 ENSESTT00000036294 Transcript intron_variant - - - - - - rs11866399 16:83683041 C 1012 NM_001220490.1 Transcript intron_variant - - - - - - rs11866399 16:83683041 C CCDS58485.1 CCDS58485.1 Transcript intron_variant - - - - - - rs11866399 16:83683041 C ENSESTG00000014477 ENSESTT00000036273 Transcript intron_variant - - - - - - rs33124 16:83851091 T ENSESTG00000005529 ENSESTT00000014109 Transcript intron_variant - - - - - - rs33124 16:83851091 T 3281 NM_001537.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4484 rs2061790 16:84432591 C CCDS42207.1 CCDS42207.1 Transcript intron_variant - - - - - - rs2061790 16:84432591 C 9914 NM_014861.2 Transcript intron_variant - - - - - - rs2061790 16:84432591 C ENSESTG00000024933 ENSESTT00000062974 Transcript intron_variant - - - - - - rs4782955 16:84437019 C ENSESTG00000024933 ENSESTT00000063210 Transcript upstream_gene_variant - - - - - - DISTANCE=3175 rs4782955 16:84437019 C ENSESTG00000024933 ENSESTT00000063191 Transcript upstream_gene_variant - - - - - - DISTANCE=3175 rs4782955 16:84437019 C ENSESTG00000024933 ENSESTT00000063179 Transcript upstream_gene_variant - - - - - - DISTANCE=3175 rs4782955 16:84437019 C ENSESTG00000024933 ENSESTT00000063165 Transcript upstream_gene_variant - - - - - - DISTANCE=3175 rs4782955 16:84437019 C CCDS42207.1 CCDS42207.1 Transcript intron_variant - - - - - - rs4782955 16:84437019 C 9914 NM_014861.2 Transcript intron_variant - - - - - - rs4782955 16:84437019 C ENSESTG00000024933 ENSESTT00000063132 Transcript upstream_gene_variant - - - - - - DISTANCE=1733 rs4782955 16:84437019 C ENSESTG00000024933 ENSESTT00000062974 Transcript intron_variant - - - - - - rs4782955 16:84437019 C ENSESTG00000024933 ENSESTT00000063222 Transcript upstream_gene_variant - - - - - - DISTANCE=3199 rs4782955 16:84437019 C ENSESTG00000024933 ENSESTT00000063120 Transcript upstream_gene_variant - - - - - - DISTANCE=1733 rs4782955 16:84437019 C ENSESTG00000024933 ENSESTT00000063193 Transcript upstream_gene_variant - - - - - - DISTANCE=3175 rs247818 16:84444349 C ENSESTG00000024933 ENSESTT00000063210 Transcript intron_variant - - - - - - rs247818 16:84444349 C ENSESTG00000024933 ENSESTT00000063191 Transcript intron_variant - - - - - - rs247818 16:84444349 C ENSESTG00000024933 ENSESTT00000063179 Transcript missense_variant 228 196 66 M/L Atg/Ctg - rs247818 16:84444349 C ENSESTG00000024933 ENSESTT00000063165 Transcript intron_variant - - - - - - rs247818 16:84444349 C CCDS42207.1 CCDS42207.1 Transcript missense_variant 493 493 165 M/L Atg/Ctg - PolyPhen=benign;SIFT=tolerated rs247818 16:84444349 C 9914 NM_014861.2 Transcript missense_variant 582 493 165 M/L Atg/Ctg - PolyPhen=benign;SIFT=tolerated rs247818 16:84444349 C ENSESTG00000024933 ENSESTT00000063132 Transcript initiator_codon_variant 289 1 1 M/L Atg/Ctg - rs247818 16:84444349 C ENSESTG00000024933 ENSESTT00000062974 Transcript missense_variant 583 493 165 M/L Atg/Ctg - rs247818 16:84444349 C ENSESTG00000024933 ENSESTT00000063222 Transcript missense_variant 482 211 71 M/L Atg/Ctg - rs247818 16:84444349 C ENSESTG00000024933 ENSESTT00000063120 Transcript initiator_codon_variant 289 1 1 M/L Atg/Ctg - rs247818 16:84444349 C ENSESTG00000024933 ENSESTT00000063193 Transcript missense_variant 228 196 66 M/L Atg/Ctg - rs555962 16:84539723 G ENSESTG00000025639 ENSESTT00000064683 Transcript intron_variant - - - - - - rs555962 16:84539723 G 57707 NM_020947.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1435 rs193701 16:84543329 C - ENSR00000511153 RegulatoryFeature regulatory_region_variant - - - - - - rs193701 16:84543329 C ENSESTG00000025639 ENSESTT00000064683 Transcript intron_variant - - - - - - rs2550414 16:84664467 C - - - intergenic_variant - - - - - - rs2911323 16:84678094 C 79786 NM_024731.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4037 rs2911323 16:84678094 C ENSESTG00000025110 ENSESTT00000063378 Transcript upstream_gene_variant - - - - - - DISTANCE=4478 rs2911323 16:84678094 C ENSESTG00000025110 ENSESTT00000063374 Transcript upstream_gene_variant - - - - - - DISTANCE=4034 rs2604952 16:84681438 T CCDS10948.1 CCDS10948.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3036 rs2604952 16:84681438 T 79786 NM_024731.2 Transcript upstream_gene_variant - - - - - - DISTANCE=693 rs2604952 16:84681438 T ENSESTG00000025110 ENSESTT00000063378 Transcript upstream_gene_variant - - - - - - DISTANCE=1134 rs2604952 16:84681438 T ENSESTG00000025110 ENSESTT00000063374 Transcript upstream_gene_variant - - - - - - DISTANCE=690 rs2966863 16:85332582 G - - - intergenic_variant - - - - - - rs7196096 16:85414774 G - - - intergenic_variant - - - - - - rs7500437 16:85614224 C - - - intergenic_variant - - - - - - rs7499587 16:85668538 C CCDS10952.1 CCDS10952.1 Transcript intron_variant - - - - - - rs7499587 16:85668538 C ENSESTG00000033776 ENSESTT00000085393 Transcript intron_variant - - - - - - rs7499587 16:85668538 C ENSESTG00000033902 ENSESTT00000085683 Transcript intron_variant - - - - - - rs7499587 16:85668538 C 23199 NM_001134473.1 Transcript intron_variant - - - - - - rs7499587 16:85668538 C ENSESTG00000033776 ENSESTT00000085387 Transcript intron_variant - - - - - - rs7499587 16:85668538 C 23199 NM_014615.2 Transcript intron_variant - - - - - - rs6539966 16:85674183 C - ENSR00000511432 RegulatoryFeature regulatory_region_variant - - - - - - rs6539966 16:85674183 C CCDS10952.1 CCDS10952.1 Transcript intron_variant - - - - - - rs6539966 16:85674183 C ENSESTG00000033776 ENSESTT00000085393 Transcript intron_variant - - - - - - rs6539966 16:85674183 C ENSESTG00000033902 ENSESTT00000085683 Transcript intron_variant - - - - - - rs6539966 16:85674183 C 23199 NM_001134473.1 Transcript intron_variant - - - - - - rs6539966 16:85674183 C ENSESTG00000033914 ENSESTT00000085709 Transcript downstream_gene_variant - - - - - - DISTANCE=3241 rs6539966 16:85674183 C ENSESTG00000033776 ENSESTT00000085387 Transcript intron_variant - - - - - - rs6539966 16:85674183 C 23199 NM_014615.2 Transcript intron_variant - - - - - - rs9938179 16:85675460 G - ENSR00001507214 RegulatoryFeature regulatory_region_variant - - - - - - rs9938179 16:85675460 G CCDS10952.1 CCDS10952.1 Transcript intron_variant - - - - - - rs9938179 16:85675460 G ENSESTG00000033776 ENSESTT00000085393 Transcript intron_variant - - - - - - rs9938179 16:85675460 G ENSESTG00000033902 ENSESTT00000085683 Transcript intron_variant - - - - - - rs9938179 16:85675460 G 23199 NM_001134473.1 Transcript intron_variant - - - - - - rs9938179 16:85675460 G ENSESTG00000033914 ENSESTT00000085709 Transcript downstream_gene_variant - - - - - - DISTANCE=1964 rs9938179 16:85675460 G ENSESTG00000033776 ENSESTT00000085387 Transcript intron_variant - - - - - - rs9938179 16:85675460 G 23199 NM_014615.2 Transcript intron_variant - - - - - - rs7192888 16:85697769 C - ENSR00001507220 RegulatoryFeature regulatory_region_variant - - - - - - rs7192888 16:85697769 C ENSESTG00000033784 ENSESTT00000085442 Transcript downstream_gene_variant - - - - - - DISTANCE=810 rs7192888 16:85697769 C ENSESTG00000033902 ENSESTT00000085683 Transcript intron_variant - - - - - - rs7192888 16:85697769 C ENSESTG00000033914 ENSESTT00000085709 Transcript intron_variant - - - - - - rs7192888 16:85697769 C CCDS10952.1 CCDS10952.1 Transcript intron_variant - - - - - - rs7192888 16:85697769 C ENSESTG00000033784 ENSESTT00000085436 Transcript intron_variant - - - - - - rs7192888 16:85697769 C 23199 NM_001134473.1 Transcript intron_variant - - - - - - rs7192888 16:85697769 C ENSESTG00000033784 ENSESTT00000085444 Transcript upstream_gene_variant - - - - - - DISTANCE=377 rs7192888 16:85697769 C CCDS45539.1 CCDS45539.1 Transcript intron_variant - - - - - - rs7192888 16:85697769 C 23199 NM_014615.2 Transcript intron_variant - - - - - - rs9930592 16:85721297 A - ENSR00000511442 RegulatoryFeature regulatory_region_variant - - - - - - rs9930592 16:85721297 A ENSESTG00000033892 ENSESTT00000085679 Transcript downstream_gene_variant - - - - - - DISTANCE=2393 rs9930592 16:85721297 A CCDS10953.1 CCDS10953.1 Transcript intron_variant - - - - - - rs9930592 16:85721297 A ENSESTG00000033902 ENSESTT00000085683 Transcript intron_variant - - - - - - rs9930592 16:85721297 A 51659 NM_016095.2 Transcript intron_variant - - - - - - rs9930592 16:85721297 A ENSESTG00000033903 ENSESTT00000085704 Transcript intron_variant - - - - - - rs396180 16:85751678 G - ENSR00000664460 RegulatoryFeature regulatory_region_variant - - - - - - rs396180 16:85751678 G CCDS45540.1 CCDS45540.1 Transcript intron_variant - - - - - - rs396180 16:85751678 G ENSESTG00000033892 ENSESTT00000085679 Transcript intron_variant - - - - - - rs396180 16:85751678 G ENSESTG00000033892 ENSESTT00000085680 Transcript intron_variant - - - - - - rs396180 16:85751678 G ENSESTG00000033892 ENSESTT00000085677 Transcript intron_variant - - - - - - rs396180 16:85751678 G ENSESTG00000033902 ENSESTT00000085683 Transcript intron_variant - - - - - - rs396180 16:85751678 G 404550 NM_206967.2 Transcript intron_variant - - - - - - rs388855 16:85775064 G ENSESTG00000033892 ENSESTT00000085679 Transcript intron_variant - - - - - - rs388855 16:85775064 G ENSESTG00000033892 ENSESTT00000085680 Transcript intron_variant - - - - - - rs388855 16:85775064 G ENSESTG00000033892 ENSESTT00000085677 Transcript intron_variant - - - - - - rs388855 16:85775064 G 100302261 NR_031731.1 Transcript downstream_gene_variant - - - - - - DISTANCE=163 rs388855 16:85775064 G 404550 NM_206967.2 Transcript intron_variant - - - - - - rs301148 16:85781839 G ENSESTG00000033892 ENSESTT00000085679 Transcript intron_variant - - - - - - rs301148 16:85781839 G ENSESTG00000033892 ENSESTT00000085680 Transcript intron_variant - - - - - - rs301148 16:85781839 G ENSESTG00000033892 ENSESTT00000085677 Transcript intron_variant - - - - - - rs301148 16:85781839 G 404550 NM_206967.2 Transcript intron_variant - - - - - - rs2432409 16:85787373 C - ENSR00001507228 RegulatoryFeature regulatory_region_variant - - - - - - rs2432409 16:85787373 C ENSESTG00000033892 ENSESTT00000085679 Transcript upstream_gene_variant - - - - - - DISTANCE=2757 rs2432409 16:85787373 C ENSESTG00000033892 ENSESTT00000085680 Transcript upstream_gene_variant - - - - - - DISTANCE=2816 rs2432409 16:85787373 C ENSESTG00000033892 ENSESTT00000085677 Transcript upstream_gene_variant - - - - - - DISTANCE=2676 rs2432409 16:85787373 C 404550 NM_206967.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2684 rs301156 16:85808045 G 10328 NM_001142288.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4185 rs301156 16:85808045 G 10328 NM_006067.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4185 rs9921665 16:85843056 C ENSESTG00000033804 ENSESTT00000085466 Transcript downstream_gene_variant - - - - - - DISTANCE=4458 rs9921665 16:85843056 C CCDS10955.1 CCDS10955.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2576 rs9921665 16:85843056 C ENSESTG00000033817 ENSESTT00000085512 Transcript downstream_gene_variant - - - - - - DISTANCE=2451 rs9921665 16:85843056 C 1327 NM_001861.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2448 rs9921665 16:85843056 C ENSESTG00000033804 ENSESTT00000085486 Transcript downstream_gene_variant - - - - - - DISTANCE=4141 rs921437 16:85866569 C - ENSR00000511471 RegulatoryFeature regulatory_region_variant - - - - - - rs921437 16:85866569 C - - - intergenic_variant - - - - - - rs446836 16:85928019 C - ENSR00001507240 RegulatoryFeature regulatory_region_variant - - - - - - rs446836 16:85928019 C 3394 NM_002163.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4755 rs446836 16:85928019 C ENSESTG00000033827 ENSESTT00000085543 Transcript upstream_gene_variant - - - - - - DISTANCE=4390 rs446836 16:85928019 C ENSESTG00000033827 ENSESTT00000085540 Transcript upstream_gene_variant - - - - - - DISTANCE=4390 rs446836 16:85928019 C ENSESTG00000033827 ENSESTT00000085548 Transcript upstream_gene_variant - - - - - - DISTANCE=4751 rs1568386 16:86025994 T - - - intergenic_variant - - - - - - rs11117440 16:86072013 C - - - intergenic_variant - - - - - - rs1687648 16:86438467 T - - - intergenic_variant - - - - - - rs367352 16:86633039 A - - - intergenic_variant - - - - - - rs7204274 16:86792884 C - - - intergenic_variant - - - - - - rs4843224 16:87218659 C ENSESTG00000013577 ENSESTT00000033952 Transcript intron_variant - - - - - - rs67926154 16:87760337 C - ENSR00000511860 RegulatoryFeature regulatory_region_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082664 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082639 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082642 Transcript intron_variant - - - - - - rs67926154 16:87760337 C CCDS54050.1 CCDS54050.1 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082725 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082677 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082672 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082669 Transcript intron_variant - - - - - - rs67926154 16:87760337 C 54758 NM_001184856.1 Transcript intron_variant - - - - - - rs67926154 16:87760337 C 54758 NM_017566.3 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082683 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082690 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082705 Transcript intron_variant - - - - - - rs67926154 16:87760337 C CCDS54051.1 CCDS54051.1 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082649 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082667 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082702 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082697 Transcript downstream_gene_variant - - - - - - DISTANCE=2587 rs67926154 16:87760337 C 54758 NM_001184854.1 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082717 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082679 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082654 Transcript intron_variant - - - - - - rs67926154 16:87760337 C CCDS10963.1 CCDS10963.1 Transcript intron_variant - - - - - - rs67926154 16:87760337 C ENSESTG00000032706 ENSESTT00000082708 Transcript intron_variant - - - - - - rs9940418 16:88150227 G - ENSR00001507420 RegulatoryFeature regulatory_region_variant - - - - - - rs9940418 16:88150227 G - - - intergenic_variant - - - - - - rs8043801 16:88205433 A - - - intergenic_variant - - - - - - rs12596483 16:88205758 G - - - intergenic_variant - - - - - - rs8182103 16:88228970 C - ENSR00001507432 RegulatoryFeature regulatory_region_variant - - - - - - rs8182103 16:88228970 C ENSESTG00000032592 ENSESTT00000082291 Transcript downstream_gene_variant - - - - - - DISTANCE=148 rs904786 16:88471927 G - - - intergenic_variant - - - - - - rs4782359 16:88486163 G - - - intergenic_variant - - - - - - rs904783 16:88504868 G CCDS45544.1 CCDS45544.1 Transcript missense_variant 10906 10906 3636 T/A Acc/Gcc - PolyPhen=benign;SIFT=tolerated rs904783 16:88504868 G 84627 NM_001127464.1 Transcript missense_variant 10906 10906 3636 T/A Acc/Gcc - PolyPhen=benign;SIFT=tolerated rs11076755 16:88507936 C CCDS45544.1 CCDS45544.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2196 rs11076755 16:88507936 C 84627 NM_001127464.1 Transcript downstream_gene_variant - - - - - - DISTANCE=771 rs554690 16:88936045 C 390748 NM_001080487.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2977 rs554690 16:88936045 C CCDS45547.2 CCDS45547.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3031 rs8051592 16:89150960 G ENSESTG00000025932 ENSESTT00000065419 Transcript upstream_gene_variant - - - - - - DISTANCE=3823 rs4785611 16:89285826 A - ENSR00000273966 RegulatoryFeature regulatory_region_variant - - - - - - rs4785611 16:89285826 A CCDS45550.1 CCDS45550.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1710 rs4785611 16:89285826 A 197320 NM_182531.3 Transcript intron_variant - - - - - - rs4785611 16:89285826 A 197320 NM_001201407.1 Transcript intron_variant - - - - - - rs4785611 16:89285826 A ENSESTG00000026816 ENSESTT00000067598 Transcript intron_variant - - - - - - rs4785611 16:89285826 A 197320 NR_037705.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2965959 16:89533919 C 29123 NM_013275.5 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000026910 ENSESTT00000067950 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000031114 ENSESTT00000078395 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000026910 ENSESTT00000067904 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000026910 ENSESTT00000067958 Transcript intron_variant - - - - - - rs2965959 16:89533919 C 29123 NM_001256182.1 Transcript intron_variant - - - - - - rs2965959 16:89533919 C 29123 NM_001256183.1 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000026910 ENSESTT00000067929 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000031114 ENSESTT00000078365 Transcript intron_variant - - - - - - rs2965959 16:89533919 C 29123 NR_045839.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000031114 ENSESTT00000078429 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000029296 ENSESTT00000073822 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000026910 ENSESTT00000067913 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000026910 ENSESTT00000067942 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000026910 ENSESTT00000067816 Transcript intron_variant - - - - - - rs2965959 16:89533919 C ENSESTG00000031114 ENSESTT00000078417 Transcript intron_variant - - - - - - rs7202091 16:89851575 A ENSESTG00000030863 ENSESTT00000077865 Transcript intron_variant - - - - - - rs7202091 16:89851575 A 2175 NM_000135.2 Transcript intron_variant - - - - - - rs7202091 16:89851575 A ENSESTG00000030934 ENSESTT00000077970 Transcript upstream_gene_variant - - - - - - DISTANCE=250 rs7202091 16:89851575 A ENSESTG00000030934 ENSESTT00000077964 Transcript upstream_gene_variant - - - - - - DISTANCE=250 rs7202091 16:89851575 A CCDS32515.1 CCDS32515.1 Transcript intron_variant - - - - - - rs67362844 17:46107 G - - - intergenic_variant - - - - - - rs9900783 17:50982 G - - - intergenic_variant - - - - - - rs4890188 17:52857 A - - - intergenic_variant - - - - - - rs4968068 17:443947 C ENSESTG00000007137 ENSESTT00000018014 Transcript downstream_gene_variant - - - - - - DISTANCE=131 rs4968068 17:443947 C ENSESTG00000007382 ENSESTT00000018666 Transcript intron_variant - - - - - - rs4968068 17:443947 C ENSESTG00000007382 ENSESTT00000018631 Transcript intron_variant - - - - - - rs4968068 17:443947 C CCDS10995.1 CCDS10995.1 Transcript intron_variant - - - - - - rs4968068 17:443947 C CCDS45558.1 CCDS45558.1 Transcript intron_variant - - - - - - rs4968068 17:443947 C 55275 NM_001128159.2 Transcript intron_variant - - - - - - rs4968068 17:443947 C 55275 NM_018289.3 Transcript intron_variant - - - - - - rs12947065 17:447617 T ENSESTG00000007137 ENSESTT00000018014 Transcript downstream_gene_variant - - - - - - DISTANCE=3801 rs12947065 17:447617 T ENSESTG00000007382 ENSESTT00000018666 Transcript intron_variant - - - - - - rs12947065 17:447617 T ENSESTG00000007382 ENSESTT00000018631 Transcript intron_variant - - - - - - rs12947065 17:447617 T CCDS10995.1 CCDS10995.1 Transcript intron_variant - - - - - - rs12947065 17:447617 T CCDS45558.1 CCDS45558.1 Transcript intron_variant - - - - - - rs12947065 17:447617 T 55275 NM_001128159.2 Transcript intron_variant - - - - - - rs12947065 17:447617 T 55275 NM_018289.3 Transcript intron_variant - - - - - - rs12942712 17:523807 C - ENSR00001533581 RegulatoryFeature regulatory_region_variant - - - - - - rs12942712 17:523807 C ENSESTG00000007382 ENSESTT00000018666 Transcript intron_variant - - - - - - rs12942712 17:523807 C ENSESTG00000007382 ENSESTT00000018631 Transcript intron_variant - - - - - - rs12942712 17:523807 C CCDS10995.1 CCDS10995.1 Transcript intron_variant - - - - - - rs12942712 17:523807 C CCDS45558.1 CCDS45558.1 Transcript intron_variant - - - - - - rs12942712 17:523807 C 55275 NM_001128159.2 Transcript intron_variant - - - - - - rs12942712 17:523807 C ENSESTG00000007382 ENSESTT00000018669 Transcript intron_variant - - - - - - rs12942712 17:523807 C 55275 NM_018289.3 Transcript intron_variant - - - - - - rs364809 17:580479 A ENSESTG00000007382 ENSESTT00000018600 Transcript intron_variant - - - - - - rs364809 17:580479 A ENSESTG00000007382 ENSESTT00000018595 Transcript intron_variant - - - - - - rs364809 17:580479 A ENSESTG00000007382 ENSESTT00000018631 Transcript intron_variant - - - - - - rs364809 17:580479 A CCDS10995.1 CCDS10995.1 Transcript intron_variant - - - - - - rs364809 17:580479 A ENSESTG00000007382 ENSESTT00000018619 Transcript intron_variant - - - - - - rs364809 17:580479 A ENSESTG00000007428 ENSESTT00000018676 Transcript intron_variant - - - - - - rs364809 17:580479 A ENSESTG00000007382 ENSESTT00000018634 Transcript intron_variant - - - - - - rs364809 17:580479 A 55275 NM_001128159.2 Transcript intron_variant - - - - - - rs364809 17:580479 A 55275 NM_018289.3 Transcript intron_variant - - - - - - rs364809 17:580479 A ENSESTG00000007382 ENSESTT00000018666 Transcript upstream_gene_variant - - - - - - DISTANCE=832 rs364809 17:580479 A CCDS45558.1 CCDS45558.1 Transcript intron_variant - - - - - - rs364809 17:580479 A ENSESTG00000007382 ENSESTT00000018669 Transcript upstream_gene_variant - - - - - - DISTANCE=832 rs393493 17:593640 C ENSESTG00000007382 ENSESTT00000018600 Transcript intron_variant - - - - - - rs393493 17:593640 C ENSESTG00000007382 ENSESTT00000018595 Transcript intron_variant - - - - - - rs393493 17:593640 C ENSESTG00000007382 ENSESTT00000018631 Transcript intron_variant - - - - - - rs393493 17:593640 C CCDS10995.1 CCDS10995.1 Transcript intron_variant - - - - - - rs393493 17:593640 C ENSESTG00000007382 ENSESTT00000018619 Transcript intron_variant - - - - - - rs393493 17:593640 C ENSESTG00000007428 ENSESTT00000018676 Transcript intron_variant - - - - - - rs393493 17:593640 C ENSESTG00000007382 ENSESTT00000018634 Transcript intron_variant - - - - - - rs393493 17:593640 C 55275 NM_001128159.2 Transcript intron_variant - - - - - - rs393493 17:593640 C 55275 NM_018289.3 Transcript intron_variant - - - - - - rs393493 17:593640 C CCDS45558.1 CCDS45558.1 Transcript intron_variant - - - - - - rs7214287 17:1099904 C ENSESTG00000017319 ENSESTT00000043560 Transcript intron_variant - - - - - - rs8080389 17:1371818 T ENSESTG00000017204 ENSESTT00000043265 Transcript intron_variant - - - - - - rs8080389 17:1371818 T CCDS42226.1 CCDS42226.1 Transcript intron_variant - - - - - - rs8080389 17:1371818 T CCDS11003.1 CCDS11003.1 Transcript intron_variant - - - - - - rs8080389 17:1371818 T ENSESTG00000017204 ENSESTT00000043232 Transcript downstream_gene_variant - - - - - - DISTANCE=3405 rs8080389 17:1371818 T 4641 NM_001080779.1 Transcript intron_variant - - - - - - rs8080389 17:1371818 T 4641 NM_033375.4 Transcript intron_variant - - - - - - rs8080389 17:1371818 T CCDS45562.1 CCDS45562.1 Transcript intron_variant - - - - - - rs8080389 17:1371818 T 4641 NM_001080950.1 Transcript intron_variant - - - - - - rs8080389 17:1371818 T ENSESTG00000017236 ENSESTT00000043275 Transcript upstream_gene_variant - - - - - - DISTANCE=627 rs8069552 17:1372008 G ENSESTG00000017204 ENSESTT00000043265 Transcript intron_variant - - - - - - rs8069552 17:1372008 G CCDS42226.1 CCDS42226.1 Transcript intron_variant - - - - - - rs8069552 17:1372008 G CCDS11003.1 CCDS11003.1 Transcript intron_variant - - - - - - rs8069552 17:1372008 G ENSESTG00000017204 ENSESTT00000043232 Transcript downstream_gene_variant - - - - - - DISTANCE=3215 rs8069552 17:1372008 G 4641 NM_001080779.1 Transcript intron_variant - - - - - - rs8069552 17:1372008 G 4641 NM_033375.4 Transcript intron_variant - - - - - - rs8069552 17:1372008 G CCDS45562.1 CCDS45562.1 Transcript intron_variant - - - - - - rs8069552 17:1372008 G 4641 NM_001080950.1 Transcript intron_variant - - - - - - rs8069552 17:1372008 G ENSESTG00000017236 ENSESTT00000043275 Transcript upstream_gene_variant - - - - - - DISTANCE=817 rs7209051 17:1728491 G ENSESTG00000016776 ENSESTT00000042254 Transcript upstream_gene_variant - - - - - - DISTANCE=4796 rs7209051 17:1728491 G 6117 NM_002945.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4782 rs7209051 17:1728491 G 114826 NM_052928.2 Transcript intron_variant - - - - - - rs7209051 17:1728491 G CCDS11014.1 CCDS11014.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4897 rs7209051 17:1728491 G ENSESTG00000016965 ENSESTT00000042599 Transcript intron_variant - - - - - - rs7209051 17:1728491 G ENSESTG00000016776 ENSESTT00000042263 Transcript upstream_gene_variant - - - - - - DISTANCE=4796 rs7209051 17:1728491 G CCDS11013.1 CCDS11013.1 Transcript intron_variant - - - - - - rs10852893 17:1818573 C - - - intergenic_variant - - - - - - rs6503254 17:2013210 C ENSESTG00000016944 ENSESTT00000042529 Transcript intron_variant - - - - - - rs6503254 17:2013210 C 23293 NM_001256828.1 Transcript intron_variant - - - - - - rs6503254 17:2013210 C ENSESTG00000030786 ENSESTT00000077687 Transcript intron_variant - - - - - - rs6503254 17:2013210 C ENSESTG00000030786 ENSESTT00000077722 Transcript intron_variant - - - - - - rs6503254 17:2013210 C 23293 NM_001256827.1 Transcript intron_variant - - - - - - rs6503254 17:2013210 C CCDS11016.1 CCDS11016.1 Transcript intron_variant - - - - - - rs6503254 17:2013210 C 23293 NM_017575.4 Transcript intron_variant - - - - - - rs6503254 17:2013210 C CCDS58498.1 CCDS58498.1 Transcript intron_variant - - - - - - rs8075849 17:2030180 C ENSESTG00000016944 ENSESTT00000042529 Transcript intron_variant - - - - - - rs8075849 17:2030180 C 23293 NM_001256828.1 Transcript intron_variant - - - - - - rs8075849 17:2030180 C ENSESTG00000030786 ENSESTT00000077687 Transcript intron_variant - - - - - - rs8075849 17:2030180 C ENSESTG00000030786 ENSESTT00000077722 Transcript intron_variant - - - - - - rs8075849 17:2030180 C 23293 NM_001256827.1 Transcript intron_variant - - - - - - rs8075849 17:2030180 C CCDS11016.1 CCDS11016.1 Transcript intron_variant - - - - - - rs8075849 17:2030180 C 23293 NM_017575.4 Transcript intron_variant - - - - - - rs8075849 17:2030180 C CCDS58498.1 CCDS58498.1 Transcript intron_variant - - - - - - rs216173 17:2164649 T ENSESTG00000030786 ENSESTT00000077624 Transcript intron_variant - - - - - - rs216173 17:2164649 T ENSESTG00000030786 ENSESTT00000077633 Transcript intron_variant - - - - - - rs216173 17:2164649 T ENSESTG00000030786 ENSESTT00000077619 Transcript intron_variant - - - - - - rs216173 17:2164649 T 23293 NM_001256827.1 Transcript intron_variant - - - - - - rs216173 17:2164649 T ENSESTG00000030786 ENSESTT00000077614 Transcript intron_variant - - - - - - rs216173 17:2164649 T CCDS11016.1 CCDS11016.1 Transcript intron_variant - - - - - - rs216173 17:2164649 T 23293 NM_017575.4 Transcript intron_variant - - - - - - rs216173 17:2164649 T ENSESTG00000030786 ENSESTT00000077635 Transcript intron_variant - - - - - - rs216177 17:2168834 A ENSESTG00000030786 ENSESTT00000077624 Transcript intron_variant - - - - - - rs216177 17:2168834 A ENSESTG00000030786 ENSESTT00000077633 Transcript intron_variant - - - - - - rs216177 17:2168834 A ENSESTG00000030786 ENSESTT00000077619 Transcript intron_variant - - - - - - rs216177 17:2168834 A 23293 NM_001256827.1 Transcript intron_variant - - - - - - rs216177 17:2168834 A ENSESTG00000030786 ENSESTT00000077614 Transcript intron_variant - - - - - - rs216177 17:2168834 A CCDS11016.1 CCDS11016.1 Transcript intron_variant - - - - - - rs216177 17:2168834 A 23293 NM_017575.4 Transcript intron_variant - - - - - - rs216177 17:2168834 A ENSESTG00000030786 ENSESTT00000077635 Transcript intron_variant - - - - - - rs6416864 17:2368184 C ENSESTG00000030533 ENSESTT00000076955 Transcript intron_variant - - - - - - rs6416864 17:2368184 C 79066 NM_024086.3 Transcript intron_variant - - - - - - rs6416864 17:2368184 C CCDS42232.1 CCDS42232.1 Transcript intron_variant - - - - - - rs7503243 17:2807427 G CCDS45573.1 CCDS45573.1 Transcript intron_variant - - - - - - rs7503243 17:2807427 G ENSESTG00000030097 ENSESTT00000075737 Transcript intron_variant - - - - - - rs7503243 17:2807427 G 23108 NM_015085.4 Transcript intron_variant - - - - - - rs7503243 17:2807427 G 23108 NM_001100398.1 Transcript intron_variant - - - - - - rs7503243 17:2807427 G CCDS45574.1 CCDS45574.1 Transcript intron_variant - - - - - - rs2317468 17:2843832 C CCDS45573.1 CCDS45573.1 Transcript intron_variant - - - - - - rs2317468 17:2843832 C ENSESTG00000030097 ENSESTT00000075737 Transcript intron_variant - - - - - - rs2317468 17:2843832 C 23108 NM_015085.4 Transcript intron_variant - - - - - - rs2317468 17:2843832 C 23108 NM_001100398.1 Transcript intron_variant - - - - - - rs2317468 17:2843832 C CCDS45574.1 CCDS45574.1 Transcript intron_variant - - - - - - rs2856272 17:3356136 T ENSESTG00000007797 ENSESTT00000019712 Transcript intron_variant - - - - - - rs2856272 17:3356136 T 84690 NM_032598.4 Transcript intron_variant - - - - - - rs2856272 17:3356136 T ENSESTG00000007797 ENSESTT00000019744 Transcript intron_variant - - - - - - rs2856272 17:3356136 T 84690 NM_001170695.1 Transcript intron_variant - - - - - - rs2856272 17:3356136 T CCDS54067.1 CCDS54067.1 Transcript intron_variant - - - - - - rs2856272 17:3356136 T 84690 NM_001170698.1 Transcript intron_variant - - - - - - rs2856272 17:3356136 T CCDS11027.1 CCDS11027.1 Transcript intron_variant - - - - - - rs2856272 17:3356136 T ENSESTG00000007797 ENSESTT00000019738 Transcript intron_variant - - - - - - rs2856272 17:3356136 T 84690 NM_001170699.1 Transcript intron_variant - - - - - - rs2856272 17:3356136 T ENSESTG00000007797 ENSESTT00000019731 Transcript intron_variant - - - - - - rs2856272 17:3356136 T 84690 NM_001170697.1 Transcript intron_variant - - - - - - rs2856272 17:3356136 T 84690 NM_001170696.1 Transcript intron_variant - - - - - - rs2856272 17:3356136 T CCDS54066.1 CCDS54066.1 Transcript intron_variant - - - - - - rs9905897 17:3442491 C ENSESTG00000007783 ENSESTT00000019668 Transcript upstream_gene_variant - - - - - - DISTANCE=3520 rs9905897 17:3442491 C CCDS11029.1 CCDS11029.1 Transcript intron_variant - - - - - - rs9905897 17:3442491 C CCDS58500.1 CCDS58500.1 Transcript intron_variant - - - - - - rs9905897 17:3442491 C 162514 NM_001258205.1 Transcript intron_variant - - - - - - rs9905897 17:3442491 C 162514 NM_145068.3 Transcript intron_variant - - - - - - rs56094622 17:3502196 A 7442 NM_080704.3 Transcript intron_variant - - - - - - rs56094622 17:3502196 A ENSESTG00000007771 ENSESTT00000019635 Transcript intron_variant - - - - - - rs56094622 17:3502196 A 7442 NM_018727.5 Transcript upstream_gene_variant - - - - - - DISTANCE=1860 rs56094622 17:3502196 A 7442 NM_080705.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3071 rs224496 17:3514028 C - ENSR00001533767 RegulatoryFeature regulatory_region_variant - - - - - - rs224496 17:3514028 C CCDS11030.1 CCDS11030.1 Transcript missense_variant 1263 1263 421 D/E gaC/gaG - PolyPhen=benign;SIFT=tolerated rs224496 17:3514028 C 7442 NM_080704.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1323 rs224496 17:3514028 C ENSESTG00000007751 ENSESTT00000019615 Transcript missense_variant 805 474 158 D/E gaC/gaG - rs224496 17:3514028 C 23729 NM_013276.2 Transcript missense_variant 1366 1263 421 D/E gaC/gaG - PolyPhen=benign;SIFT=tolerated rs224496 17:3514028 C ENSESTG00000007751 ENSESTT00000019609 Transcript missense_variant 1321 1263 421 D/E gaC/gaG - PolyPhen=benign;SIFT=tolerated rs224496 17:3514028 C ENSESTG00000007771 ENSESTT00000019635 Transcript upstream_gene_variant - - - - - - DISTANCE=1355 rs224516 17:3529471 C CCDS11030.1 CCDS11030.1 Transcript intron_variant - - - - - - rs224516 17:3529471 C ENSESTG00000007751 ENSESTT00000019615 Transcript intron_variant - - - - - - rs224516 17:3529471 C 23729 NM_013276.2 Transcript intron_variant - - - - - - rs224516 17:3529471 C ENSESTG00000007751 ENSESTT00000019609 Transcript intron_variant - - - - - - rs161352 17:3551616 C 1497 NM_001031681.2 Transcript intron_variant - - - - - - rs161352 17:3551616 C ENSESTG00000007444 ENSESTT00000018759 Transcript intron_variant - - - - - - rs161352 17:3551616 C 1497 NM_004937.2 Transcript intron_variant - - - - - - rs161352 17:3551616 C CCDS11031.1 CCDS11031.1 Transcript intron_variant - - - - - - rs161352 17:3551616 C ENSESTG00000007444 ENSESTT00000018738 Transcript downstream_gene_variant - - - - - - DISTANCE=854 rs161352 17:3551616 C ENSESTG00000007444 ENSESTT00000018745 Transcript intron_variant - - - - - - rs161352 17:3551616 C ENSESTG00000007444 ENSESTT00000018733 Transcript intron_variant - - - - - - rs161352 17:3551616 C ENSESTG00000007749 ENSESTT00000019550 Transcript intron_variant - - - - - - rs161352 17:3551616 C CCDS32530.1 CCDS32530.1 Transcript intron_variant - - - - - - rs2654681 17:3584972 C CCDS11034.1 CCDS11034.1 Transcript intron_variant - - - - - - rs2654681 17:3584972 C ENSESTG00000007704 ENSESTT00000019455 Transcript upstream_gene_variant - - - - - - DISTANCE=2028 rs2654681 17:3584972 C ENSESTG00000007470 ENSESTT00000018816 Transcript downstream_gene_variant - - - - - - DISTANCE=3971 rs2654681 17:3584972 C ENSESTG00000007704 ENSESTT00000019429 Transcript intron_variant - - - - - - rs2654681 17:3584972 C ENSESTG00000007704 ENSESTT00000019433 Transcript downstream_gene_variant - - - - - - DISTANCE=3842 rs2654681 17:3584972 C 100533970 NR_037928.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2654681 17:3584972 C CCDS11035.1 CCDS11035.1 Transcript intron_variant - - - - - - rs2654681 17:3584972 C 5026 NM_002561.3 Transcript intron_variant - - - - - - rs2654681 17:3584972 C 5026 NM_001204519.1 Transcript intron_variant - - - - - - rs2654681 17:3584972 C CCDS56014.1 CCDS56014.1 Transcript intron_variant - - - - - - rs2654681 17:3584972 C 5026 NM_001204520.1 Transcript intron_variant - - - - - - rs2654681 17:3584972 C 5026 NM_175080.2 Transcript intron_variant - - - - - - rs2654681 17:3584972 C CCDS56015.1 CCDS56015.1 Transcript intron_variant - - - - - - rs9905739 17:3706274 G - ENSR00001339338 RegulatoryFeature regulatory_region_variant - - - - - - rs9905739 17:3706274 G CCDS32531.1 CCDS32531.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1836 rs9905739 17:3706274 G 3682 NM_002208.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1737 rs9905739 17:3706274 G 55421 NM_001114118.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3768 rs7502345 17:3708968 C CCDS32531.1 CCDS32531.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4530 rs7502345 17:3708968 C 3682 NM_002208.4 Transcript upstream_gene_variant - - - - - - DISTANCE=4431 rs7502345 17:3708968 C 55421 NM_001114118.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1074 rs184566 17:4402803 C - ENSR00001339521 RegulatoryFeature regulatory_region_variant - - - - - - rs184566 17:4402803 C 124976 NM_001124758.1 Transcript intron_variant - - - - - - rs184566 17:4402803 C CCDS42237.1 CCDS42237.1 Transcript intron_variant - - - - - - rs4790707 17:4709588 T CCDS11057.1 CCDS11057.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1480 rs4790707 17:4709588 T 5338 NM_001243108.1 Transcript upstream_gene_variant - - - - - - DISTANCE=808 rs4790707 17:4709588 T ENSESTG00000016836 ENSESTT00000042401 Transcript upstream_gene_variant - - - - - - DISTANCE=888 rs4790707 17:4709588 T 5338 NM_002663.4 Transcript upstream_gene_variant - - - - - - DISTANCE=808 rs4790707 17:4709588 T ENSESTG00000016836 ENSESTT00000042411 Transcript upstream_gene_variant - - - - - - DISTANCE=1269 rs4790707 17:4709588 T ENSESTG00000016836 ENSESTT00000042318 Transcript upstream_gene_variant - - - - - - DISTANCE=874 rs4790707 17:4709588 T CCDS58507.1 CCDS58507.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1480 rs4790707 17:4709588 T ENSESTG00000017542 ENSESTT00000044135 Transcript downstream_gene_variant - - - - - - DISTANCE=3617 rs2661698 17:4820812 G - - - intergenic_variant - - - - - - rs2661699 17:4820980 G - - - intergenic_variant - - - - - - rs2661700 17:4820996 C - - - intergenic_variant - - - - - - rs4287625 17:4940979 A 55065 NM_017986.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2252 rs4287625 17:4940979 A CCDS11066.1 CCDS11066.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3078 rs4287625 17:4940979 A 55065 NM_001104577.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2252 rs4790737 17:4974312 G - - - intergenic_variant - - - - - - rs7214137 17:4977876 T 124961 NM_153018.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3878 rs7214137 17:4977876 T ENSESTG00000027482 ENSESTT00000069182 Transcript upstream_gene_variant - - - - - - DISTANCE=3878 rs7226115 17:5011809 G CCDS11068.1 CCDS11068.1 Transcript intron_variant - - - - - - rs7226115 17:5011809 G ENSESTG00000028243 ENSESTT00000071025 Transcript downstream_gene_variant - - - - - - DISTANCE=3297 rs7226115 17:5011809 G 7775 NM_014519.2 Transcript intron_variant - - - - - - rs4644905 17:5050148 A CCDS11069.2 CCDS11069.2 Transcript intron_variant - - - - - - rs4644905 17:5050148 A 9098 NM_004505.2 Transcript intron_variant - - - - - - rs4644905 17:5050148 A ENSESTG00000027517 ENSESTT00000069270 Transcript intron_variant - - - - - - rs8069482 17:5065387 C - ENSR00001339716 RegulatoryFeature regulatory_region_variant - - - - - - rs8069482 17:5065387 C CCDS11069.2 CCDS11069.2 Transcript intron_variant - - - - - - rs8069482 17:5065387 C ENSESTG00000027526 ENSESTT00000069283 Transcript intron_variant - - - - - - rs8069482 17:5065387 C 9098 NM_004505.2 Transcript intron_variant - - - - - - rs2467305 17:5073730 G CCDS11069.2 CCDS11069.2 Transcript intron_variant - - - - - - rs2467305 17:5073730 G ENSESTG00000027531 ENSESTT00000069304 Transcript upstream_gene_variant - - - - - - DISTANCE=84 rs2467305 17:5073730 G ENSESTG00000027526 ENSESTT00000069283 Transcript downstream_gene_variant - - - - - - DISTANCE=2374 rs2467305 17:5073730 G 9098 NM_004505.2 Transcript intron_variant - - - - - - rs2463964 17:5104577 T ENSESTG00000027539 ENSESTT00000069326 Transcript intron_variant - - - - - - rs2463964 17:5104577 T 100130950 NR_034082.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4790795 17:5547464 G - - - intergenic_variant - - - - - - rs2535582 17:5634233 T - - - intergenic_variant - - - - - - rs4401089 17:6049872 T - - - intergenic_variant - - - - - - rs4284697 17:6060115 C - - - intergenic_variant - - - - - - rs1872237 17:6198860 C - - - intergenic_variant - - - - - - rs6502950 17:6298232 G ENSESTG00000025944 ENSESTT00000065540 Transcript intron_variant - - - - - - rs7503716 17:7045353 C - - - intergenic_variant - - - - - - rs4344809 17:7417086 A 5430 NM_000937.4 Transcript missense_variant 5889 5503 1835 A/T Gcc/Acc - PolyPhen=unknown;SIFT=tolerated rs4344809 17:7417086 A ENSESTG00000004407 ENSESTT00000011169 Transcript downstream_gene_variant - - - - - - DISTANCE=1752 rs4344809 17:7417086 A ENSESTG00000004407 ENSESTT00000011164 Transcript downstream_gene_variant - - - - - - DISTANCE=339 rs4344809 17:7417086 A CCDS32548.1 CCDS32548.1 Transcript missense_variant 5503 5503 1835 A/T Gcc/Acc - PolyPhen=unknown;SIFT=tolerated rs4344809 17:7417086 A ENSESTG00000004363 ENSESTT00000011012 Transcript missense_variant 131 130 44 A/T Gcc/Acc - rs8080692 17:7764597 G ENSESTG00000004903 ENSESTT00000012474 Transcript intron_variant - - - - - - rs8080692 17:7764597 G 124637 NM_144607.4 Transcript 3_prime_UTR_variant 2743 - - - - - rs8080692 17:7764597 G ENSESTG00000004701 ENSESTT00000011865 Transcript downstream_gene_variant - - - - - - DISTANCE=2489 rs8080692 17:7764597 G ENSESTG00000004903 ENSESTT00000012479 Transcript intron_variant - - - - - - rs8080692 17:7764597 G CCDS11122.1 CCDS11122.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3856 rs8080692 17:7764597 G CCDS11123.1 CCDS11123.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1667 rs8080692 17:7764597 G 84316 NM_032356.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3425 rs7406836 17:7794898 G ENSESTG00000004717 ENSESTT00000012088 Transcript upstream_gene_variant - - - - - - DISTANCE=1704 rs7406836 17:7794898 G ENSESTG00000004717 ENSESTT00000011925 Transcript downstream_gene_variant - - - - - - DISTANCE=897 rs7406836 17:7794898 G CCDS32554.1 CCDS32554.1 Transcript intron_variant - - - - - - rs7406836 17:7794898 G CCDS32553.2 CCDS32553.2 Transcript intron_variant - - - - - - rs7406836 17:7794898 G ENSESTG00000004717 ENSESTT00000011939 Transcript intron_variant - - - - - - rs7406836 17:7794898 G CCDS32555.1 CCDS32555.1 Transcript intron_variant - - - - - - rs7406836 17:7794898 G ENSESTG00000004717 ENSESTT00000012093 Transcript upstream_gene_variant - - - - - - DISTANCE=2540 rs7406836 17:7794898 G 1107 NM_001005271.2 Transcript intron_variant - - - - - - rs7406836 17:7794898 G 1107 NM_001005273.2 Transcript intron_variant - - - - - - rs7406836 17:7794898 G 1107 NM_005852.3 Transcript intron_variant - - - - - - rs7221216 17:7845637 T ENSESTG00000004790 ENSESTT00000012180 Transcript intron_variant - - - - - - rs7221216 17:7845637 T ENSESTG00000004790 ENSESTT00000012198 Transcript intron_variant - - - - - - rs7221216 17:7845637 T CCDS32557.1 CCDS32557.1 Transcript intron_variant - - - - - - rs7221216 17:7845637 T ENSESTG00000004790 ENSESTT00000012200 Transcript intron_variant - - - - - - rs7221216 17:7845637 T ENSESTG00000004790 ENSESTT00000012182 Transcript intron_variant - - - - - - rs7221216 17:7845637 T 116840 NM_053051.3 Transcript intron_variant - - - - - - rs7221216 17:7845637 T CCDS11126.1 CCDS11126.1 Transcript intron_variant - - - - - - rs7221216 17:7845637 T ENSESTG00000004790 ENSESTT00000012189 Transcript intron_variant - - - - - - rs7221216 17:7845637 T 116840 NM_001037144.5 Transcript intron_variant - - - - - - rs11658559 17:7870279 C - - - intergenic_variant - - - - - - rs9909784 17:7991330 G - ENSR00001340372 RegulatoryFeature regulatory_region_variant - - - - - - rs9909784 17:7991330 G 242 NM_001139.2 Transcript upstream_gene_variant - - - - - - DISTANCE=309 rs9909784 17:7991330 G 100422983 NR_036201.1 Transcript upstream_gene_variant - - - - - - DISTANCE=44 rs9909784 17:7991330 G ENSESTG00000003055 ENSESTT00000007625 Transcript upstream_gene_variant - - - - - - DISTANCE=671 rs9909784 17:7991330 G CCDS11129.1 CCDS11129.1 Transcript upstream_gene_variant - - - - - - DISTANCE=570 rs6503093 17:8141707 C CCDS42259.1 CCDS42259.1 Transcript splice_region_variant,intron_variant - - - - - - rs6503093 17:8141707 C ENSESTG00000002983 ENSESTT00000007434 Transcript splice_region_variant,intron_variant - - - - - - rs6503093 17:8141707 C ENSESTG00000002983 ENSESTT00000007430 Transcript splice_region_variant,intron_variant - - - - - - rs6503093 17:8141707 C 80169 NM_025099.5 Transcript splice_region_variant,intron_variant - - - - - - rs6503093 17:8141707 C 80169 NR_046431.1 Transcript splice_region_variant,intron_variant,nc_transcript_variant - - - - - - rs12950614 17:8180995 G - - - intergenic_variant - - - - - - rs3895790 17:9229182 G 9482 NM_004853.2 Transcript intron_variant - - - - - - rs3895790 17:9229182 G 9482 NR_033656.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3895790 17:9229182 G CCDS32565.1 CCDS32565.1 Transcript intron_variant - - - - - - rs3895790 17:9229182 G ENSESTG00000016239 ENSESTT00000040789 Transcript intron_variant - - - - - - rs6503270 17:9807710 T 5957 NM_002903.2 Transcript intron_variant - - - - - - rs6503270 17:9807710 T CCDS11151.1 CCDS11151.1 Transcript intron_variant - - - - - - rs4791387 17:10046379 A ENSESTG00000027185 ENSESTT00000068502 Transcript intron_variant - - - - - - rs4791387 17:10046379 A 8522 NM_201433.1 Transcript intron_variant - - - - - - rs4791387 17:10046379 A CCDS11152.1 CCDS11152.1 Transcript intron_variant - - - - - - rs4791387 17:10046379 A ENSESTG00000016167 ENSESTT00000040583 Transcript intron_variant - - - - - - rs4791388 17:10046469 A ENSESTG00000027185 ENSESTT00000068502 Transcript intron_variant - - - - - - rs4791388 17:10046469 A 8522 NM_201433.1 Transcript intron_variant - - - - - - rs4791388 17:10046469 A CCDS11152.1 CCDS11152.1 Transcript intron_variant - - - - - - rs4791388 17:10046469 A ENSESTG00000016167 ENSESTT00000040583 Transcript intron_variant - - - - - - rs2904900 17:10069116 C ENSESTG00000027185 ENSESTT00000068502 Transcript intron_variant - - - - - - rs2904900 17:10069116 C 8522 NM_201433.1 Transcript intron_variant - - - - - - rs2904900 17:10069116 C CCDS11152.1 CCDS11152.1 Transcript intron_variant - - - - - - rs2904900 17:10069116 C ENSESTG00000016167 ENSESTT00000040583 Transcript intron_variant - - - - - - rs201598 17:10527472 T - ENSR00001534228 RegulatoryFeature regulatory_region_variant - - - - - - rs201598 17:10527472 T ENSESTG00000027612 ENSESTT00000069519 Transcript downstream_gene_variant - - - - - - DISTANCE=4379 rs201598 17:10527472 T ENSESTG00000027227 ENSESTT00000068604 Transcript downstream_gene_variant - - - - - - DISTANCE=1119 rs201598 17:10527472 T CCDS11157.1 CCDS11157.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4498 rs201598 17:10527472 T ENSESTG00000027612 ENSESTT00000069491 Transcript downstream_gene_variant - - - - - - DISTANCE=4377 rs201598 17:10527472 T ENSESTG00000027245 ENSESTT00000068625 Transcript 3_prime_UTR_variant 308 - - - - - rs201598 17:10527472 T 4621 NM_002470.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4371 rs201598 17:10527472 T ENSESTG00000027227 ENSESTT00000068613 Transcript downstream_gene_variant - - - - - - DISTANCE=1244 rs2040570 17:10584116 T 6341 NM_004589.2 Transcript 3_prime_UTR_variant 1287 - - - - - rs2040570 17:10584116 T ENSESTG00000027251 ENSESTT00000068640 Transcript downstream_gene_variant - - - - - - DISTANCE=1320 rs2040570 17:10584116 T ENSESTG00000027575 ENSESTT00000069436 Transcript 3_prime_UTR_variant 622 - - - - - rs2040570 17:10584116 T CCDS11158.1 CCDS11158.1 Transcript downstream_gene_variant - - - - - - DISTANCE=320 rs427999 17:10612853 A 56985 NM_020233.4 Transcript intron_variant - - - - - - rs427999 17:10612853 A 388335 NM_001004313.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3786 rs427999 17:10612853 A CCDS11159.2 CCDS11159.2 Transcript intron_variant - - - - - - rs427999 17:10612853 A ENSESTG00000027259 ENSESTT00000068713 Transcript intron_variant - - - - - - rs427999 17:10612853 A ENSESTG00000027259 ENSESTT00000068749 Transcript intron_variant - - - - - - rs8074465 17:10738727 G ENSESTG00000027470 ENSESTT00000069160 Transcript intron_variant - - - - - - rs8074465 17:10738727 G 644139 NM_001101387.1 Transcript intron_variant - - - - - - rs2943037 17:11337652 T CCDS54089.1 CCDS54089.1 Transcript intron_variant - - - - - - rs2943037 17:11337652 T ENSESTG00000006893 ENSESTT00000017532 Transcript intron_variant - - - - - - rs2943037 17:11337652 T CCDS54090.1 CCDS54090.1 Transcript intron_variant - - - - - - rs2943037 17:11337652 T 388336 NM_001173462.1 Transcript intron_variant - - - - - - rs2943037 17:11337652 T 388336 NM_001173461.1 Transcript intron_variant - - - - - - rs2943037 17:11337652 T CCDS45615.1 CCDS45615.1 Transcript intron_variant - - - - - - rs2943037 17:11337652 T 388336 NM_207386.3 Transcript intron_variant - - - - - - rs2943037 17:11337652 T ENSESTG00000006998 ENSESTT00000017722 Transcript intron_variant - - - - - - rs4791478 17:11743834 C 1770 NM_001372.3 Transcript intron_variant - - - - - - rs4791478 17:11743834 C CCDS11160.1 CCDS11160.1 Transcript intron_variant - - - - - - rs2005732 17:12141648 C - - - intergenic_variant - - - - - - rs1380661 17:12164728 T - - - intergenic_variant - - - - - - rs7212739 17:12176692 A - - - intergenic_variant - - - - - - rs2054290 17:12185639 G - ENSR00001341041 RegulatoryFeature regulatory_region_variant - - - - - - rs2054290 17:12185639 G - - - intergenic_variant - - - - - - rs2529716 17:12191694 C - - - intergenic_variant - - - - - - rs2041090 17:12271140 T - - - intergenic_variant - - - - - - rs2190661 17:12275722 C - - - intergenic_variant - - - - - - rs9303076 17:13095943 A - - - intergenic_variant - - - - - - rs2674940 17:13141961 G - - - intergenic_variant - - - - - - rs10852814 17:13372918 A - - - intergenic_variant - - - - - - rs765476 17:13570647 C - - - intergenic_variant - - - - - - rs4792398 17:13693060 G - - - intergenic_variant - - - - - - rs2170369 17:14301204 C - - - intergenic_variant - - - - - - rs493869 17:14367919 C - - - intergenic_variant - - - - - - rs2430190 17:14396788 T - - - intergenic_variant - - - - - - rs9303109 17:14476486 A - - - intergenic_variant - - - - - - rs4792575 17:15050873 A - - - intergenic_variant - - - - - - rs9897703 17:15065762 T - - - intergenic_variant - - - - - - rs443879 17:15228811 G CCDS11169.1 CCDS11169.1 Transcript intron_variant - - - - - - rs443879 17:15228811 G 64518 NM_031898.2 Transcript intron_variant - - - - - - rs12603370 17:15306528 G - - - intergenic_variant - - - - - - rs4792662 17:15650170 G 353149 NM_178571.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2072 rs4792662 17:15650170 G CCDS42265.1 CCDS42265.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4828 rs4792662 17:15650170 G ENSESTG00000033855 ENSESTT00000085605 Transcript downstream_gene_variant - - - - - - DISTANCE=2073 rs6502550 17:16890782 A - ENSR00001341777 RegulatoryFeature regulatory_region_variant - - - - - - rs6502550 17:16890782 A - - - intergenic_variant - - - - - - rs8072964 17:16969893 C CCDS42268.1 CCDS42268.1 Transcript intron_variant - - - - - - rs8072964 17:16969893 C 23164 NM_201274.3 Transcript intron_variant - - - - - - rs8072964 17:16969893 C ENSESTG00000001722 ENSESTT00000004374 Transcript intron_variant - - - - - - rs8072964 17:16969893 C ENSESTG00000001722 ENSESTT00000004364 Transcript intron_variant - - - - - - rs8072964 17:16969893 C ENSESTG00000001722 ENSESTT00000004358 Transcript intron_variant - - - - - - rs8072964 17:16969893 C ENSESTG00000001722 ENSESTT00000004349 Transcript intron_variant - - - - - - rs8072964 17:16969893 C 23164 NM_015134.3 Transcript intron_variant - - - - - - rs8072964 17:16969893 C ENSESTG00000001722 ENSESTT00000004365 Transcript intron_variant - - - - - - rs8072964 17:16969893 C CCDS32578.1 CCDS32578.1 Transcript intron_variant - - - - - - rs7219779 17:17450445 G CCDS58520.1 CCDS58520.1 Transcript intron_variant - - - - - - rs7219779 17:17450445 G 10400 NM_001267551.1 Transcript intron_variant - - - - - - rs7219779 17:17450445 G 10400 NM_148173.1 Transcript intron_variant - - - - - - rs7219779 17:17450445 G CCDS11186.1 CCDS11186.1 Transcript intron_variant - - - - - - rs7219779 17:17450445 G ENSESTG00000002010 ENSESTT00000005052 Transcript intron_variant - - - - - - rs7219779 17:17450445 G 10400 NM_001267552.1 Transcript intron_variant - - - - - - rs7219779 17:17450445 G CCDS11187.1 CCDS11187.1 Transcript intron_variant - - - - - - rs7219779 17:17450445 G 10400 NM_007169.2 Transcript intron_variant - - - - - - rs7219779 17:17450445 G ENSESTG00000002010 ENSESTT00000005041 Transcript intron_variant - - - - - - rs7219779 17:17450445 G 10400 NM_148172.2 Transcript intron_variant - - - - - - rs7503754 17:17474967 C CCDS58520.1 CCDS58520.1 Transcript intron_variant - - - - - - rs7503754 17:17474967 C 10400 NM_001267551.1 Transcript intron_variant - - - - - - rs7503754 17:17474967 C 10400 NM_148173.1 Transcript intron_variant - - - - - - rs7503754 17:17474967 C CCDS11186.1 CCDS11186.1 Transcript intron_variant - - - - - - rs7503754 17:17474967 C ENSESTG00000002010 ENSESTT00000005052 Transcript intron_variant - - - - - - rs7503754 17:17474967 C 10400 NM_001267552.1 Transcript intron_variant - - - - - - rs7503754 17:17474967 C CCDS11187.1 CCDS11187.1 Transcript intron_variant - - - - - - rs7503754 17:17474967 C 10400 NM_007169.2 Transcript intron_variant - - - - - - rs7503754 17:17474967 C ENSESTG00000002010 ENSESTT00000005041 Transcript intron_variant - - - - - - rs7503754 17:17474967 C 10400 NM_148172.2 Transcript intron_variant - - - - - - rs9906117 17:17573154 C - - - intergenic_variant - - - - - - rs4616339 17:17855863 G ENSESTG00000001918 ENSESTT00000004771 Transcript intron_variant - - - - - - rs4616339 17:17855863 G ENSESTG00000001918 ENSESTT00000004785 Transcript intron_variant - - - - - - rs4616339 17:17855863 G 146691 NM_001033551.2 Transcript intron_variant - - - - - - rs4616339 17:17855863 G ENSESTG00000001918 ENSESTT00000004760 Transcript intron_variant - - - - - - rs4616339 17:17855863 G CCDS42270.1 CCDS42270.1 Transcript intron_variant - - - - - - rs4616339 17:17855863 G ENSESTG00000001918 ENSESTT00000004786 Transcript intron_variant - - - - - - rs4616339 17:17855863 G 146691 NM_001082968.1 Transcript intron_variant - - - - - - rs4616339 17:17855863 G CCDS32584.1 CCDS32584.1 Transcript intron_variant - - - - - - rs9908505 17:18031493 C CCDS42271.1 CCDS42271.1 Transcript intron_variant - - - - - - rs9908505 17:18031493 C 51168 NM_016239.3 Transcript intron_variant - - - - - - rs4303606 17:18052466 G ENSESTG00000021786 ENSESTT00000054900 Transcript upstream_gene_variant - - - - - - DISTANCE=4903 rs4303606 17:18052466 G ENSESTG00000021786 ENSESTT00000054856 Transcript upstream_gene_variant - - - - - - DISTANCE=4555 rs4303606 17:18052466 G ENSESTG00000021786 ENSESTT00000054874 Transcript upstream_gene_variant - - - - - - DISTANCE=4903 rs4303606 17:18052466 G CCDS42271.1 CCDS42271.1 Transcript intron_variant - - - - - - rs4303606 17:18052466 G ENSESTG00000021786 ENSESTT00000054808 Transcript upstream_gene_variant - - - - - - DISTANCE=4243 rs4303606 17:18052466 G 51168 NM_016239.3 Transcript intron_variant - - - - - - rs4924838 17:18102995 G ENSESTG00000021865 ENSESTT00000055065 Transcript intron_variant - - - - - - rs4924838 17:18102995 G 54890 NM_017758.3 Transcript intron_variant - - - - - - rs4924838 17:18102995 G CCDS42272.1 CCDS42272.1 Transcript intron_variant - - - - - - rs35332008 17:19756026 C 9706 NM_014683.3 Transcript intron_variant - - - - - - rs35332008 17:19756026 C 9706 NM_001142610.1 Transcript intron_variant - - - - - - rs35332008 17:19756026 C ENSESTG00000035439 ENSESTT00000089529 Transcript intron_variant - - - - - - rs35332008 17:19756026 C CCDS11213.1 CCDS11213.1 Transcript intron_variant - - - - - - rs35332008 17:19756026 C ENSESTG00000035439 ENSESTT00000089528 Transcript intron_variant - - - - - - rs35332008 17:19756026 C ENSESTG00000035439 ENSESTT00000089526 Transcript intron_variant - - - - - - rs2542885 17:20003248 C ENSESTG00000033381 ENSESTT00000084344 Transcript intron_variant - - - - - - rs2542885 17:20003248 C CCDS32590.1 CCDS32590.1 Transcript intron_variant - - - - - - rs2542885 17:20003248 C ENSESTG00000033381 ENSESTT00000084319 Transcript intron_variant - - - - - - rs2542885 17:20003248 C 92521 NM_152904.4 Transcript intron_variant - - - - - - rs2542885 17:20003248 C ENSESTG00000033381 ENSESTT00000084334 Transcript intron_variant - - - - - - rs2542885 17:20003248 C ENSESTG00000033381 ENSESTT00000084313 Transcript intron_variant - - - - - - rs2542885 17:20003248 C CCDS42280.1 CCDS42280.1 Transcript intron_variant - - - - - - rs2542885 17:20003248 C 92521 NM_001243439.1 Transcript intron_variant - - - - - - rs2542885 17:20003248 C ENSESTG00000033381 ENSESTT00000084322 Transcript downstream_gene_variant - - - - - - DISTANCE=3227 rs2542885 17:20003248 C 92521 NM_001033553.2 Transcript intron_variant - - - - - - rs55672271 17:20506957 G - - - intergenic_variant - - - - - - rs11653710 17:20725991 G - - - intergenic_variant - - - - - - rs9325903 17:21211286 G CCDS11217.1 CCDS11217.1 Transcript intron_variant - - - - - - rs9325903 17:21211286 G ENSESTG00000017926 ENSESTT00000045386 Transcript intron_variant - - - - - - rs9325903 17:21211286 G CCDS11218.1 CCDS11218.1 Transcript intron_variant - - - - - - rs9325903 17:21211286 G ENSESTG00000018087 ENSESTT00000045506 Transcript intron_variant - - - - - - rs9325903 17:21211286 G 5606 NM_145109.2 Transcript intron_variant - - - - - - rs9325903 17:21211286 G 5606 NM_002756.4 Transcript intron_variant - - - - - - rs8081596 17:21265643 G - - - intergenic_variant - - - - - - rs6587159 17:21431484 C 339263 NM_001113434.3 Transcript downstream_gene_variant - - - - - - DISTANCE=87 rs9898706 17:21788525 A - - - intergenic_variant - - - - - - rs12952483 17:21837266 T - ENSR00001342961 RegulatoryFeature regulatory_region_variant - - - - - - rs12952483 17:21837266 T - - - intergenic_variant - - - - - - rs10853130 17:25459599 G - - - intergenic_variant - - - - - - rs6505135 17:25516454 T - - - intergenic_variant - - - - - - rs322204 17:25689633 A - - - intergenic_variant - - - - - - rs7501616 17:25707139 G - ENSR00001343079 RegulatoryFeature regulatory_region_variant - - - - - - rs7501616 17:25707139 G - - - intergenic_variant - - - - - - rs2948531 17:25869193 G 8844 NM_014238.1 Transcript intron_variant - - - - - - rs2948531 17:25869193 G ENSESTG00000026742 ENSESTT00000067372 Transcript intron_variant - - - - - - rs2948531 17:25869193 G ENSESTG00000026742 ENSESTT00000067338 Transcript intron_variant - - - - - - rs2948531 17:25869193 G ENSESTG00000026742 ENSESTT00000067323 Transcript intron_variant - - - - - - rs4267373 17:25944235 G ENSESTG00000026785 ENSESTT00000067755 Transcript upstream_gene_variant - - - - - - DISTANCE=3836 rs4267373 17:25944235 G 8844 NM_014238.1 Transcript intron_variant - - - - - - rs4267373 17:25944235 G CCDS58532.1 CCDS58532.1 Transcript intron_variant - - - - - - rs4267373 17:25944235 G ENSESTG00000026785 ENSESTT00000067727 Transcript intron_variant - - - - - - rs4267373 17:25944235 G ENSESTG00000026785 ENSESTT00000067707 Transcript intron_variant - - - - - - rs4267373 17:25944235 G ENSESTG00000026785 ENSESTT00000067700 Transcript intron_variant - - - - - - rs4267373 17:25944235 G ENSESTG00000026785 ENSESTT00000067627 Transcript intron_variant - - - - - - rs9905778 17:26292203 C - ENSR00001343240 RegulatoryFeature regulatory_region_variant - - - - - - rs9905778 17:26292203 C - - - intergenic_variant - - - - - - rs8068865 17:26702238 G ENSESTG00000027257 ENSESTT00000068704 Transcript intron_variant - - - - - - rs8068865 17:26702238 G ENSESTG00000027317 ENSESTT00000068806 Transcript intron_variant - - - - - - rs8068865 17:26702238 G 7448 NM_000638.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4865 rs8068865 17:26702238 G 23098 NM_015077.2 Transcript intron_variant - - - - - - rs8068865 17:26702238 G ENSESTG00000027257 ENSESTT00000068771 Transcript intron_variant - - - - - - rs8068865 17:26702238 G ENSESTG00000027411 ENSESTT00000069022 Transcript upstream_gene_variant - - - - - - DISTANCE=2128 rs756768 17:26727377 G 113235 NM_080669.4 Transcript intron_variant - - - - - - rs756768 17:26727377 G 23098 NM_015077.2 Transcript 3_prime_UTR_variant 6312 - - - - - rs756768 17:26727377 G ENSESTG00000027383 ENSESTT00000068983 Transcript intron_variant - - - - - - rs756768 17:26727377 G 113235 NM_001242366.1 Transcript intron_variant - - - - - - rs756768 17:26727377 G ENSESTG00000027383 ENSESTT00000069002 Transcript intron_variant - - - - - - rs756768 17:26727377 G ENSESTG00000027383 ENSESTT00000068974 Transcript intron_variant - - - - - - rs756768 17:26727377 G ENSESTG00000027365 ENSESTT00000068927 Transcript upstream_gene_variant - - - - - - DISTANCE=3986 rs1471999 17:27288984 G ENSESTG00000001369 ENSESTT00000003277 Transcript intron_variant - - - - - - rs1471999 17:27288984 G 124925 NM_178860.4 Transcript intron_variant - - - - - - rs1471999 17:27288984 G ENSESTG00000001369 ENSESTT00000003280 Transcript intron_variant - - - - - - rs1471999 17:27288984 G 124925 NM_001098635.1 Transcript intron_variant - - - - - - rs1471999 17:27288984 G CCDS45639.1 CCDS45639.1 Transcript intron_variant - - - - - - rs1471999 17:27288984 G CCDS45638.1 CCDS45638.1 Transcript intron_variant - - - - - - rs1471999 17:27288984 G ENSESTG00000001369 ENSESTT00000003290 Transcript upstream_gene_variant - - - - - - DISTANCE=1114 rs7406299 17:27481684 C ENSESTG00000001216 ENSESTT00000002879 Transcript intron_variant - - - - - - rs7406299 17:27481684 C CCDS45642.1 CCDS45642.1 Transcript intron_variant - - - - - - rs7406299 17:27481684 C 399687 NM_203318.1 Transcript intron_variant - - - - - - rs7406299 17:27481684 C 399687 NM_078471.3 Transcript intron_variant - - - - - - rs7406299 17:27481684 C CCDS45641.1 CCDS45641.1 Transcript intron_variant - - - - - - rs6505110 17:27492516 G ENSESTG00000001272 ENSESTT00000003001 Transcript downstream_gene_variant - - - - - - DISTANCE=1121 rs6505110 17:27492516 G ENSESTG00000001272 ENSESTT00000002996 Transcript downstream_gene_variant - - - - - - DISTANCE=949 rs6505110 17:27492516 G CCDS45642.1 CCDS45642.1 Transcript intron_variant - - - - - - rs6505110 17:27492516 G 399687 NM_203318.1 Transcript intron_variant - - - - - - rs6505110 17:27492516 G 399687 NM_078471.3 Transcript intron_variant - - - - - - rs6505110 17:27492516 G CCDS45641.1 CCDS45641.1 Transcript intron_variant - - - - - - rs6505116 17:27548032 C - - - intergenic_variant - - - - - - rs1712653 17:27669532 G - - - intergenic_variant - - - - - - rs9893762 17:28453614 T ENSESTG00000033577 ENSESTT00000084926 Transcript intron_variant - - - - - - rs9893762 17:28453614 T 84081 NM_001261467.1 Transcript intron_variant - - - - - - rs9893762 17:28453614 T ENSESTG00000033577 ENSESTT00000084883 Transcript intron_variant - - - - - - rs9893762 17:28453614 T CCDS11255.1 CCDS11255.1 Transcript intron_variant - - - - - - rs9893762 17:28453614 T ENSESTG00000033577 ENSESTT00000084914 Transcript intron_variant - - - - - - rs9893762 17:28453614 T 84081 NM_032141.3 Transcript intron_variant - - - - - - rs9893762 17:28453614 T ENSESTG00000033577 ENSESTT00000084893 Transcript intron_variant - - - - - - rs6505174 17:28646137 C CCDS32605.1 CCDS32605.1 Transcript intron_variant - - - - - - rs6505174 17:28646137 C 388364 NM_206832.1 Transcript intron_variant - - - - - - rs6505174 17:28646137 C ENSESTG00000033623 ENSESTT00000084993 Transcript intron_variant - - - - - - rs216413 17:28902613 C 147172 NR_015341.2 Transcript upstream_gene_variant - - - - - - DISTANCE=870 rs216413 17:28902613 C ENSESTG00000025589 ENSESTT00000064586 Transcript upstream_gene_variant - - - - - - DISTANCE=870 rs216413 17:28902613 C ENSESTG00000025589 ENSESTT00000064565 Transcript upstream_gene_variant - - - - - - DISTANCE=870 rs216413 17:28902613 C ENSESTG00000025589 ENSESTT00000064624 Transcript upstream_gene_variant - - - - - - DISTANCE=904 rs216413 17:28902613 C ENSESTG00000025589 ENSESTT00000064599 Transcript upstream_gene_variant - - - - - - DISTANCE=870 rs216413 17:28902613 C ENSESTG00000027283 ENSESTT00000068725 Transcript intron_variant - - - - - - rs9891948 17:29259201 C ENSESTG00000025811 ENSESTT00000065232 Transcript intron_variant - - - - - - rs9891948 17:29259201 C ENSESTG00000025811 ENSESTT00000065178 Transcript intron_variant - - - - - - rs9891948 17:29259201 C CCDS11261.1 CCDS11261.1 Transcript intron_variant - - - - - - rs9891948 17:29259201 C 55803 NM_018404.2 Transcript intron_variant - - - - - - rs9891948 17:29259201 C ENSESTG00000025811 ENSESTT00000065218 Transcript intron_variant - - - - - - rs9891948 17:29259201 C ENSESTG00000025811 ENSESTT00000065165 Transcript intron_variant - - - - - - rs7502717 17:29730916 G 84440 NM_032932.3 Transcript intron_variant - - - - - - rs7502717 17:29730916 G CCDS11267.1 CCDS11267.1 Transcript intron_variant - - - - - - rs7502717 17:29730916 G ENSESTG00000010890 ENSESTT00000027293 Transcript intron_variant - - - - - - rs9303644 17:29808108 G 84440 NM_032932.3 Transcript intron_variant - - - - - - rs9303644 17:29808108 G CCDS11267.1 CCDS11267.1 Transcript intron_variant - - - - - - rs9303644 17:29808108 G ENSESTG00000010890 ENSESTT00000027293 Transcript intron_variant - - - - - - rs9303644 17:29808108 G ENSESTG00000010890 ENSESTT00000027295 Transcript intron_variant - - - - - - rs797313 17:29918684 T - - - intergenic_variant - - - - - - rs223137 17:29932125 C - - - intergenic_variant - - - - - - rs386811 17:30065849 A - - - intergenic_variant - - - - - - rs301349 17:30542801 A CCDS32610.1 CCDS32610.1 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027631 Transcript intron_variant - - - - - - rs301349 17:30542801 A 55288 NM_018307.3 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027648 Transcript intron_variant - - - - - - rs301349 17:30542801 A 55288 NM_001033566.1 Transcript intron_variant - - - - - - rs301349 17:30542801 A CCDS32611.1 CCDS32611.1 Transcript intron_variant - - - - - - rs301349 17:30542801 A 55288 NM_001033568.1 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027574 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027651 Transcript intron_variant - - - - - - rs301349 17:30542801 A CCDS32612.1 CCDS32612.1 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027610 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027656 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027615 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027588 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027658 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027612 Transcript intron_variant - - - - - - rs301349 17:30542801 A ENSESTG00000010982 ENSESTT00000027617 Transcript intron_variant - - - - - - rs4794920 17:30711186 C ENSESTG00000005951 ENSESTT00000015080 Transcript intron_variant - - - - - - rs2909516 17:30944285 G 4642 NM_015194.1 Transcript intron_variant - - - - - - rs2909516 17:30944285 G ENSESTG00000006061 ENSESTT00000015355 Transcript intron_variant - - - - - - rs2909516 17:30944285 G CCDS32615.1 CCDS32615.1 Transcript intron_variant - - - - - - rs2466833 17:31172619 A ENSESTG00000006054 ENSESTT00000015309 Transcript intron_variant - - - - - - rs2466833 17:31172619 A 4642 NM_015194.1 Transcript intron_variant - - - - - - rs2466833 17:31172619 A CCDS32615.1 CCDS32615.1 Transcript intron_variant - - - - - - rs172772 17:31564320 G ENSESTG00000006046 ENSESTT00000015296 Transcript intron_variant - - - - - - rs172772 17:31564320 G ENSESTG00000006046 ENSESTT00000015298 Transcript intron_variant - - - - - - rs172772 17:31564320 G 40 NM_001094.4 Transcript intron_variant - - - - - - rs172772 17:31564320 G CCDS11276.1 CCDS11276.1 Transcript intron_variant - - - - - - rs172772 17:31564320 G CCDS42296.1 CCDS42296.1 Transcript intron_variant - - - - - - rs172772 17:31564320 G 40 NM_183377.1 Transcript intron_variant - - - - - - rs4795756 17:31588164 A ENSESTG00000006046 ENSESTT00000015296 Transcript intron_variant - - - - - - rs4795756 17:31588164 A ENSESTG00000006046 ENSESTT00000015298 Transcript intron_variant - - - - - - rs4795756 17:31588164 A 40 NM_001094.4 Transcript intron_variant - - - - - - rs4795756 17:31588164 A CCDS11276.1 CCDS11276.1 Transcript intron_variant - - - - - - rs4795756 17:31588164 A CCDS42296.1 CCDS42296.1 Transcript intron_variant - - - - - - rs4795756 17:31588164 A 40 NM_183377.1 Transcript intron_variant - - - - - - rs9303664 17:31908622 G 40 NM_001094.4 Transcript intron_variant - - - - - - rs9303664 17:31908622 G CCDS42296.1 CCDS42296.1 Transcript intron_variant - - - - - - rs280050 17:31983960 G 40 NM_001094.4 Transcript intron_variant - - - - - - rs280050 17:31983960 G CCDS42296.1 CCDS42296.1 Transcript intron_variant - - - - - - rs2637342 17:32178253 C 40 NM_001094.4 Transcript intron_variant - - - - - - rs2637342 17:32178253 C CCDS42296.1 CCDS42296.1 Transcript intron_variant - - - - - - rs391201 17:32219915 T 40 NM_001094.4 Transcript intron_variant - - - - - - rs391201 17:32219915 T CCDS42296.1 CCDS42296.1 Transcript intron_variant - - - - - - rs317340 17:32294288 T 40 NM_001094.4 Transcript intron_variant - - - - - - rs317340 17:32294288 T CCDS42296.1 CCDS42296.1 Transcript intron_variant - - - - - - rs295084 17:32732408 A - - - intergenic_variant - - - - - - rs4796019 17:33251877 G CCDS54106.1 CCDS54106.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4796019 17:33251877 G 10693 NM_006584.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3001 rs4796019 17:33251877 G CCDS32617.1 CCDS32617.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4796019 17:33251877 G ENSESTG00000000255 ENSESTT00000000647 Transcript downstream_gene_variant - - - - - - DISTANCE=3072 rs4796019 17:33251877 G 10693 NM_001193530.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3001 rs4796019 17:33251877 G CCDS54105.1 CCDS54105.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4796019 17:33251877 G 10693 NM_001193529.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3001 rs1384139 17:33260346 G ENSESTG00000000255 ENSESTT00000000648 Transcript intron_variant - - - - - - rs1384139 17:33260346 G CCDS32617.1 CCDS32617.1 Transcript intron_variant - - - - - - rs1384139 17:33260346 G ENSESTG00000000255 ENSESTT00000000647 Transcript intron_variant - - - - - - rs1384139 17:33260346 G CCDS54105.1 CCDS54105.1 Transcript intron_variant - - - - - - rs1384139 17:33260346 G 10693 NM_006584.3 Transcript intron_variant - - - - - - rs1384139 17:33260346 G CCDS54106.1 CCDS54106.1 Transcript intron_variant - - - - - - rs1384139 17:33260346 G 10693 NM_001193530.1 Transcript intron_variant - - - - - - rs1384139 17:33260346 G 10693 NM_001193529.1 Transcript intron_variant - - - - - - rs1913546 17:33667219 T - - - intergenic_variant - - - - - - rs6505467 17:33695618 G ENSESTG00000011831 ENSESTT00000029655 Transcript intron_variant - - - - - - rs6505467 17:33695618 G CCDS11294.1 CCDS11294.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4792 rs6505467 17:33695618 G 91607 NM_001104589.1 Transcript intron_variant - - - - - - rs6505467 17:33695618 G 91607 NM_001104590.1 Transcript intron_variant - - - - - - rs6505467 17:33695618 G 91607 NM_001104587.1 Transcript intron_variant - - - - - - rs6505467 17:33695618 G 91607 NM_001104588.1 Transcript intron_variant - - - - - - rs6505467 17:33695618 G ENSESTG00000011850 ENSESTT00000029698 Transcript intron_variant - - - - - - rs6505467 17:33695618 G 91607 NM_152270.3 Transcript intron_variant - - - - - - rs8067192 17:33695943 G ENSESTG00000011831 ENSESTT00000029655 Transcript intron_variant - - - - - - rs8067192 17:33695943 G 91607 NM_001104589.1 Transcript intron_variant - - - - - - rs8067192 17:33695943 G 91607 NM_001104588.1 Transcript intron_variant - - - - - - rs8067192 17:33695943 G ENSESTG00000011850 ENSESTT00000029698 Transcript intron_variant - - - - - - rs8067192 17:33695943 G 91607 NM_001104590.1 Transcript intron_variant - - - - - - rs8067192 17:33695943 G 91607 NM_152270.3 Transcript intron_variant - - - - - - rs8067192 17:33695943 G 91607 NM_001104587.1 Transcript intron_variant - - - - - - rs809535 17:33740392 A ENSESTG00000011831 ENSESTT00000029655 Transcript intron_variant - - - - - - rs809535 17:33740392 A ENSESTG00000011841 ENSESTT00000029683 Transcript intron_variant - - - - - - rs809535 17:33740392 A 55106 NM_018042.3 Transcript intron_variant - - - - - - rs809535 17:33740392 A CCDS11295.1 CCDS11295.1 Transcript intron_variant - - - - - - rs2671826 17:33761995 G ENSESTG00000011831 ENSESTT00000029655 Transcript intron_variant - - - - - - rs2671826 17:33761995 G ENSESTG00000011835 ENSESTT00000029674 Transcript upstream_gene_variant - - - - - - DISTANCE=1800 rs2671826 17:33761995 G 146857 NM_144682.5 Transcript downstream_gene_variant - - - - - - DISTANCE=120 rs2671826 17:33761995 G 55106 NM_018042.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2452 rs9303688 17:33795463 A - ENSR00001344779 RegulatoryFeature regulatory_region_variant - - - - - - rs9303688 17:33795463 A ENSESTG00000011815 ENSESTT00000029628 Transcript intron_variant - - - - - - rs6505488 17:33998584 T ENSESTG00000011389 ENSESTT00000028752 Transcript intron_variant - - - - - - rs6505488 17:33998584 T CCDS32622.1 CCDS32622.1 Transcript intron_variant - - - - - - rs6505488 17:33998584 T ENSESTG00000011389 ENSESTT00000028735 Transcript intron_variant - - - - - - rs6505488 17:33998584 T 163 NM_001282.2 Transcript intron_variant - - - - - - rs6505488 17:33998584 T ENSESTG00000011389 ENSESTT00000028747 Transcript intron_variant - - - - - - rs6505488 17:33998584 T ENSESTG00000011389 ENSESTT00000028733 Transcript intron_variant - - - - - - rs6505488 17:33998584 T CCDS32621.1 CCDS32621.1 Transcript intron_variant - - - - - - rs6505488 17:33998584 T ENSESTG00000011389 ENSESTT00000028706 Transcript intron_variant - - - - - - rs6505488 17:33998584 T ENSESTG00000011389 ENSESTT00000028709 Transcript intron_variant - - - - - - rs6505488 17:33998584 T ENSESTG00000011389 ENSESTT00000028750 Transcript intron_variant - - - - - - rs6505488 17:33998584 T ENSESTG00000011389 ENSESTT00000028695 Transcript intron_variant - - - - - - rs6505488 17:33998584 T 163 NM_001030006.1 Transcript intron_variant - - - - - - rs6505488 17:33998584 T ENSESTG00000011389 ENSESTT00000028737 Transcript intron_variant - - - - - - rs3859283 17:34006220 T ENSESTG00000011389 ENSESTT00000028752 Transcript intron_variant - - - - - - rs3859283 17:34006220 T CCDS32622.1 CCDS32622.1 Transcript intron_variant - - - - - - rs3859283 17:34006220 T ENSESTG00000011389 ENSESTT00000028735 Transcript intron_variant - - - - - - rs3859283 17:34006220 T 163 NM_001282.2 Transcript intron_variant - - - - - - rs3859283 17:34006220 T ENSESTG00000011389 ENSESTT00000028747 Transcript intron_variant - - - - - - rs3859283 17:34006220 T ENSESTG00000011389 ENSESTT00000028733 Transcript intron_variant - - - - - - rs3859283 17:34006220 T CCDS32621.1 CCDS32621.1 Transcript intron_variant - - - - - - rs3859283 17:34006220 T ENSESTG00000011389 ENSESTT00000028706 Transcript intron_variant - - - - - - rs3859283 17:34006220 T ENSESTG00000011389 ENSESTT00000028709 Transcript intron_variant - - - - - - rs3859283 17:34006220 T ENSESTG00000011389 ENSESTT00000028750 Transcript intron_variant - - - - - - rs3859283 17:34006220 T ENSESTG00000011389 ENSESTT00000028695 Transcript intron_variant - - - - - - rs3859283 17:34006220 T 163 NM_001030006.1 Transcript intron_variant - - - - - - rs3859283 17:34006220 T ENSESTG00000011389 ENSESTT00000028737 Transcript intron_variant - - - - - - rs226425 17:34054007 T - ENSR00001535494 RegulatoryFeature regulatory_region_variant - - - - - - rs226425 17:34054007 T ENSESTG00000011456 ENSESTT00000028798 Transcript downstream_gene_variant - - - - - - DISTANCE=2902 rs226425 17:34054007 T ENSESTG00000011488 ENSESTT00000028836 Transcript upstream_gene_variant - - - - - - DISTANCE=4661 rs226425 17:34054007 T CCDS32622.1 CCDS32622.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3289 rs226425 17:34054007 T ENSESTG00000011488 ENSESTT00000028840 Transcript upstream_gene_variant - - - - - - DISTANCE=4661 rs226425 17:34054007 T 163 NM_001282.2 Transcript downstream_gene_variant - - - - - - DISTANCE=571 rs226425 17:34054007 T ENSESTG00000011488 ENSESTT00000028834 Transcript upstream_gene_variant - - - - - - DISTANCE=4661 rs226425 17:34054007 T CCDS32621.1 CCDS32621.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3289 rs226425 17:34054007 T 91608 NM_033315.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4672 rs226425 17:34054007 T 163 NM_001030006.1 Transcript downstream_gene_variant - - - - - - DISTANCE=571 rs226431 17:34100826 T ENSESTG00000011799 ENSESTT00000029600 Transcript intron_variant - - - - - - rs226431 17:34100826 T 79148 NM_001032278.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4683 rs226431 17:34100826 T 79148 NM_024302.3 Transcript intron_variant - - - - - - rs226430 17:34114248 C - ENSR00001344857 RegulatoryFeature regulatory_region_variant - - - - - - rs226430 17:34114248 C ENSESTG00000011795 ENSESTT00000029586 Transcript intron_variant - - - - - - rs226430 17:34114248 C ENSESTG00000011795 ENSESTT00000029591 Transcript upstream_gene_variant - - - - - - DISTANCE=2726 rs226430 17:34114248 C CCDS45651.1 CCDS45651.1 Transcript intron_variant - - - - - - rs226430 17:34114248 C 79148 NM_001032278.1 Transcript intron_variant - - - - - - rs226430 17:34114248 C 79148 NM_024302.3 Transcript intron_variant - - - - - - rs2120277 17:35011359 T - - - intergenic_variant - - - - - - rs1561971 17:35043159 T - - - intergenic_variant - - - - - - rs4795140 17:35049419 T - - - intergenic_variant - - - - - - rs9916662 17:35107915 G - - - intergenic_variant - - - - - - rs295837 17:35168330 C - - - intergenic_variant - - - - - - rs4539651 17:35372871 A ENSESTG00000020175 ENSESTT00000050813 Transcript intron_variant - - - - - - rs4539651 17:35372871 A ENSESTG00000020175 ENSESTT00000050588 Transcript intron_variant - - - - - - rs4539651 17:35372871 A 26574 NM_012138.3 Transcript intron_variant - - - - - - rs4539651 17:35372871 A CCDS32632.1 CCDS32632.1 Transcript intron_variant - - - - - - rs4539651 17:35372871 A ENSESTG00000020175 ENSESTT00000050820 Transcript upstream_gene_variant - - - - - - DISTANCE=3430 rs1470452 17:35478362 C 31 NM_198839.1 Transcript synonymous_variant 7376 6078 2026 T acA/acG - rs1470452 17:35478362 C 31 NM_198838.1 Transcript synonymous_variant 6450 5844 1948 T acA/acG - rs1470452 17:35478362 C ENSESTG00000020582 ENSESTT00000051844 Transcript intron_variant - - - - - - rs1470452 17:35478362 C 31 NM_198834.1 Transcript synonymous_variant 6702 6189 2063 T acA/acG - rs1470452 17:35478362 C 31 NM_198837.1 Transcript synonymous_variant 6339 5904 1968 T acA/acG - rs1470452 17:35478362 C ENSESTG00000020582 ENSESTT00000052144 Transcript synonymous_variant 2669 2532 844 T acA/acG - rs1470452 17:35478362 C 31 NM_198836.1 Transcript synonymous_variant 6269 6078 2026 T acA/acG - rs1470452 17:35478362 C CCDS11317.1 CCDS11317.1 Transcript synonymous_variant 6078 6078 2026 T acA/acG - rs1470452 17:35478362 C CCDS11318.1 CCDS11318.1 Transcript synonymous_variant 5904 5904 1968 T acA/acG - rs1470452 17:35478362 C CCDS42302.1 CCDS42302.1 Transcript synonymous_variant 6189 6189 2063 T acA/acG - rs1470452 17:35478362 C CCDS42303.1 CCDS42303.1 Transcript synonymous_variant 5844 5844 1948 T acA/acG - rs4794749 17:35527120 T 31 NM_198839.1 Transcript intron_variant - - - - - - rs4794749 17:35527120 T 31 NM_198838.1 Transcript intron_variant - - - - - - rs4794749 17:35527120 T ENSESTG00000020582 ENSESTT00000051844 Transcript intron_variant - - - - - - rs4794749 17:35527120 T 31 NM_198834.1 Transcript intron_variant - - - - - - rs4794749 17:35527120 T 31 NM_198837.1 Transcript intron_variant - - - - - - rs4794749 17:35527120 T ENSESTG00000020582 ENSESTT00000052144 Transcript intron_variant - - - - - - rs4794749 17:35527120 T 31 NM_198836.1 Transcript intron_variant - - - - - - rs4794749 17:35527120 T CCDS11317.1 CCDS11317.1 Transcript intron_variant - - - - - - rs4794749 17:35527120 T CCDS11318.1 CCDS11318.1 Transcript intron_variant - - - - - - rs4794749 17:35527120 T CCDS42302.1 CCDS42302.1 Transcript intron_variant - - - - - - rs4794749 17:35527120 T CCDS42303.1 CCDS42303.1 Transcript intron_variant - - - - - - rs6607276 17:35874989 A ENSESTG00000011053 ENSESTT00000027722 Transcript downstream_gene_variant - - - - - - DISTANCE=3796 rs6607276 17:35874989 A CCDS11320.1 CCDS11320.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2018 rs6607276 17:35874989 A 11276 NM_001163546.1 Transcript 3_prime_UTR_variant 7677 - - - - - rs6607276 17:35874989 A ENSESTG00000010798 ENSESTT00000027055 Transcript downstream_gene_variant - - - - - - DISTANCE=1395 rs6607276 17:35874989 A 11276 NM_080550.3 Transcript 3_prime_UTR_variant 7812 - - - - - rs6607276 17:35874989 A CCDS11322.2 CCDS11322.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4054 rs6607276 17:35874989 A ENSESTG00000010798 ENSESTT00000027049 Transcript downstream_gene_variant - - - - - - DISTANCE=1395 rs6607276 17:35874989 A ENSESTG00000011053 ENSESTT00000027723 Transcript downstream_gene_variant - - - - - - DISTANCE=4112 rs6607276 17:35874989 A 11276 NM_007247.4 Transcript 3_prime_UTR_variant 8082 - - - - - rs6607276 17:35874989 A 11276 NM_001163545.1 Transcript 3_prime_UTR_variant 7845 - - - - - rs6607276 17:35874989 A 11276 NM_001163544.1 Transcript 3_prime_UTR_variant 7848 - - - - - rs6607276 17:35874989 A CCDS54114.1 CCDS54114.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4054 rs6607276 17:35874989 A 11072 NM_007026.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1401 rs6607276 17:35874989 A ENSESTG00000011053 ENSESTT00000027710 Transcript downstream_gene_variant - - - - - - DISTANCE=4156 rs6607276 17:35874989 A CCDS11321.1 CCDS11321.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4054 rs6607276 17:35874989 A ENSESTG00000011053 ENSESTT00000027724 Transcript downstream_gene_variant - - - - - - DISTANCE=4124 rs6607276 17:35874989 A 11276 NM_001163547.1 Transcript 3_prime_UTR_variant 7464 - - - - - rs6607276 17:35874989 A ENSESTG00000010798 ENSESTT00000027029 Transcript downstream_gene_variant - - - - - - DISTANCE=2467 rs6607276 17:35874989 A 11276 NM_198882.1 Transcript 3_prime_UTR_variant 7917 - - - - - rs6607276 17:35874989 A CCDS54113.1 CCDS54113.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4054 rs2158236 17:35888432 C ENSESTG00000011053 ENSESTT00000027722 Transcript intron_variant - - - - - - rs2158236 17:35888432 C CCDS54114.1 CCDS54114.1 Transcript intron_variant - - - - - - rs2158236 17:35888432 C 11276 NM_001163546.1 Transcript intron_variant - - - - - - rs2158236 17:35888432 C 11276 NM_080550.3 Transcript intron_variant - - - - - - rs2158236 17:35888432 C CCDS11322.2 CCDS11322.2 Transcript intron_variant - - - - - - rs2158236 17:35888432 C ENSESTG00000011053 ENSESTT00000027710 Transcript intron_variant - - - - - - rs2158236 17:35888432 C CCDS11321.1 CCDS11321.1 Transcript intron_variant - - - - - - rs2158236 17:35888432 C ENSESTG00000011053 ENSESTT00000027724 Transcript intron_variant - - - - - - rs2158236 17:35888432 C 11276 NM_001163547.1 Transcript intron_variant - - - - - - rs2158236 17:35888432 C 11276 NM_198882.1 Transcript intron_variant - - - - - - rs2158236 17:35888432 C ENSESTG00000011053 ENSESTT00000027723 Transcript intron_variant - - - - - - rs2158236 17:35888432 C 11276 NM_007247.4 Transcript intron_variant - - - - - - rs2158236 17:35888432 C CCDS54113.1 CCDS54113.1 Transcript intron_variant - - - - - - rs2158236 17:35888432 C 11276 NM_001163544.1 Transcript intron_variant - - - - - - rs2158236 17:35888432 C 11276 NM_001163545.1 Transcript intron_variant - - - - - - rs9900406 17:35968987 A - ENSR00001345235 RegulatoryFeature regulatory_region_variant - - - - - - rs9900406 17:35968987 A CCDS54114.1 CCDS54114.1 Transcript intron_variant - - - - - - rs9900406 17:35968987 A 11276 NM_001163546.1 Transcript intron_variant - - - - - - rs9900406 17:35968987 A 11056 NM_007010.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3376 rs9900406 17:35968987 A 11276 NM_080550.3 Transcript intron_variant - - - - - - rs9900406 17:35968987 A CCDS11322.2 CCDS11322.2 Transcript intron_variant - - - - - - rs9900406 17:35968987 A CCDS11321.1 CCDS11321.1 Transcript intron_variant - - - - - - rs9900406 17:35968987 A 11276 NM_001163547.1 Transcript intron_variant - - - - - - rs9900406 17:35968987 A 11276 NM_198882.1 Transcript intron_variant - - - - - - rs9900406 17:35968987 A ENSESTG00000011018 ENSESTT00000027666 Transcript intron_variant - - - - - - rs9900406 17:35968987 A 11276 NM_007247.4 Transcript intron_variant - - - - - - rs9900406 17:35968987 A CCDS54113.1 CCDS54113.1 Transcript intron_variant - - - - - - rs9900406 17:35968987 A 11276 NM_001163544.1 Transcript intron_variant - - - - - - rs9900406 17:35968987 A 11276 NM_001163545.1 Transcript intron_variant - - - - - - rs7503988 17:36602620 T CCDS56027.1 CCDS56027.1 Transcript intron_variant - - - - - - rs7503988 17:36602620 T 57636 NM_001199417.1 Transcript intron_variant - - - - - - rs7503988 17:36602620 T ENSESTG00000010900 ENSESTT00000027299 Transcript intron_variant - - - - - - rs7225780 17:36701784 C CCDS45660.1 CCDS45660.1 Transcript intron_variant - - - - - - rs7225780 17:36701784 C ENSESTG00000004499 ENSESTT00000011355 Transcript intron_variant - - - - - - rs7225780 17:36701784 C 80725 NM_025248.2 Transcript intron_variant - - - - - - rs17855918 17:36861983 C - ENSR00001345474 RegulatoryFeature regulatory_region_variant - - - - - - rs17855918 17:36861983 C ENSESTG00000004110 ENSESTT00000010434 Transcript missense_variant 109 98 33 V/A gTc/gCc - rs17855918 17:36861983 C ENSESTG00000004110 ENSESTT00000010440 Transcript upstream_gene_variant - - - - - - DISTANCE=3350 rs17855918 17:36861983 C 4302 NM_005937.3 Transcript missense_variant 111 98 33 V/A gTc/gCc - PolyPhen=unknown;SIFT=tolerated rs17855918 17:36861983 C 100616203 NR_039887.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3399 rs17855918 17:36861983 C ENSESTG00000004110 ENSESTT00000010429 Transcript missense_variant 111 98 33 V/A gTc/gCc - rs17855918 17:36861983 C CCDS11327.1 CCDS11327.1 Transcript missense_variant 98 98 33 V/A gTc/gCc - PolyPhen=unknown;SIFT=tolerated rs2715548 17:38566396 A CCDS45672.1 CCDS45672.1 Transcript intron_variant - - - - - - rs2715548 17:38566396 A ENSESTG00000019413 ENSESTT00000048771 Transcript intron_variant - - - - - - rs2715548 17:38566396 A 7153 NM_001067.3 Transcript intron_variant - - - - - - rs2957099 17:38839301 C - - - intergenic_variant - - - - - - rs2429556 17:38892942 T - - - intergenic_variant - - - - - - rs1116106 17:39477113 G - - - intergenic_variant - - - - - - rs4890085 17:39572463 C - ENSR00001535867 RegulatoryFeature regulatory_region_variant - - - - - - rs4890085 17:39572463 C 8688 NM_003770.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4346 rs4890085 17:39572463 C CCDS32653.1 CCDS32653.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4667 rs4890085 17:39572463 C ENSESTG00000008529 ENSESTT00000021431 Transcript upstream_gene_variant - - - - - - DISTANCE=4670 rs4890085 17:39572463 C 100505782 NR_040111.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3623 rs4890085 17:39572463 C ENSESTG00000008522 ENSESTT00000021427 Transcript intron_variant - - - - - - rs7214720 17:39722691 T CCDS32654.1 CCDS32654.1 Transcript downstream_gene_variant - - - - - - DISTANCE=834 rs7214720 17:39722691 T 3857 NM_000226.3 Transcript intron_variant - - - - - - rs7214720 17:39722691 T ENSESTG00000020969 ENSESTT00000052745 Transcript intron_variant - - - - - - rs116976632 17:39755193 G ENSESTG00000020969 ENSESTT00000052745 Transcript intron_variant - - - - - - rs8080490 17:39815347 G - - - intergenic_variant - - - - - - rs8073865 17:39826948 T - - - intergenic_variant - - - - - - rs12453367 17:39949653 C - ENSR00001346366 RegulatoryFeature regulatory_region_variant - - - - - - rs12453367 17:39949653 C - - - intergenic_variant - - - - - - rs9898794 17:40518388 A ENSESTG00000021089 ENSESTT00000053247 Transcript intron_variant - - - - - - rs9898794 17:40518388 A ENSESTG00000021089 ENSESTT00000053185 Transcript intron_variant - - - - - - rs9898794 17:40518388 A 6774 NM_139276.2 Transcript intron_variant - - - - - - rs9898794 17:40518388 A 6774 NM_213662.1 Transcript intron_variant - - - - - - rs9898794 17:40518388 A ENSESTG00000021089 ENSESTT00000053171 Transcript intron_variant - - - - - - rs9898794 17:40518388 A ENSESTG00000021089 ENSESTT00000053213 Transcript intron_variant - - - - - - rs9898794 17:40518388 A 6774 NM_003150.3 Transcript intron_variant - - - - - - rs7208263 17:40565545 C - ENSR00001346568 RegulatoryFeature regulatory_region_variant - - - - - - rs7208263 17:40565545 C ENSESTG00000021066 ENSESTT00000052895 Transcript intron_variant - - - - - - rs7208263 17:40565545 C 284119 NM_012232.5 Transcript intron_variant - - - - - - rs7208263 17:40565545 C CCDS11425.1 CCDS11425.1 Transcript intron_variant - - - - - - rs4796586 17:40611789 G - ENSR00001346587 RegulatoryFeature regulatory_region_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032989 Transcript intron_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032999 Transcript upstream_gene_variant - - - - - - DISTANCE=412 rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032993 Transcript upstream_gene_variant - - - - - - DISTANCE=412 rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032966 Transcript intron_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032961 Transcript intron_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032986 Transcript intron_variant - - - - - - rs4796586 17:40611789 G CCDS45683.1 CCDS45683.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1124 rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000033001 Transcript upstream_gene_variant - - - - - - DISTANCE=412 rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032996 Transcript upstream_gene_variant - - - - - - DISTANCE=412 rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032991 Transcript intron_variant - - - - - - rs4796586 17:40611789 G 535 NM_005177.3 Transcript intron_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032977 Transcript intron_variant - - - - - - rs4796586 17:40611789 G 535 NM_001130020.1 Transcript intron_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032987 Transcript intron_variant - - - - - - rs4796586 17:40611789 G CCDS45684.1 CCDS45684.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1124 rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032980 Transcript intron_variant - - - - - - rs4796586 17:40611789 G CCDS11426.1 CCDS11426.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1124 rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032982 Transcript intron_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032973 Transcript intron_variant - - - - - - rs4796586 17:40611789 G 535 NM_001130021.1 Transcript intron_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032998 Transcript upstream_gene_variant - - - - - - DISTANCE=412 rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032975 Transcript intron_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000032983 Transcript intron_variant - - - - - - rs4796586 17:40611789 G ENSESTG00000013123 ENSESTT00000033003 Transcript upstream_gene_variant - - - - - - DISTANCE=412 rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032989 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032999 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032993 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032966 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032961 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032986 Transcript intron_variant - - - - - - rs11079048 17:40631693 G CCDS45683.1 CCDS45683.1 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000033001 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032996 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032991 Transcript intron_variant - - - - - - rs11079048 17:40631693 G 535 NM_005177.3 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032977 Transcript intron_variant - - - - - - rs11079048 17:40631693 G 535 NM_001130020.1 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032987 Transcript intron_variant - - - - - - rs11079048 17:40631693 G CCDS45684.1 CCDS45684.1 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032980 Transcript intron_variant - - - - - - rs11079048 17:40631693 G CCDS11426.1 CCDS11426.1 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032982 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032973 Transcript intron_variant - - - - - - rs11079048 17:40631693 G 535 NM_001130021.1 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032998 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032975 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000032983 Transcript intron_variant - - - - - - rs11079048 17:40631693 G ENSESTG00000013123 ENSESTT00000033003 Transcript intron_variant - - - - - - rs6503718 17:40836374 C ENSESTG00000013313 ENSESTT00000033439 Transcript upstream_gene_variant - - - - - - DISTANCE=3570 rs6503718 17:40836374 C ENSESTG00000013313 ENSESTT00000033433 Transcript upstream_gene_variant - - - - - - DISTANCE=3570 rs6503718 17:40836374 C ENSESTG00000013935 ENSESTT00000034813 Transcript upstream_gene_variant - - - - - - DISTANCE=439 rs6503718 17:40836374 C CCDS11435.1 CCDS11435.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2533 rs6503718 17:40836374 C 8506 NM_003632.2 Transcript intron_variant - - - - - - rs6503718 17:40836374 C ENSESTG00000013302 ENSESTT00000033355 Transcript downstream_gene_variant - - - - - - DISTANCE=2257 rs6503718 17:40836374 C ENSESTG00000013928 ENSESTT00000034808 Transcript intron_variant - - - - - - rs6503718 17:40836374 C 2826 NM_016602.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2529 rs6503718 17:40836374 C ENSESTG00000013305 ENSESTT00000033367 Transcript intron_variant - - - - - - rs6503718 17:40836374 C CCDS11436.1 CCDS11436.1 Transcript intron_variant - - - - - - rs9889691 17:40869436 C ENSESTG00000013893 ENSESTT00000034772 Transcript downstream_gene_variant - - - - - - DISTANCE=557 rs9889691 17:40869436 C 2145 NM_001991.3 Transcript intron_variant - - - - - - rs9889691 17:40869436 C CCDS32659.1 CCDS32659.1 Transcript intron_variant - - - - - - rs9889691 17:40869436 C ENSESTG00000013893 ENSESTT00000034778 Transcript intron_variant - - - - - - rs9889691 17:40869436 C ENSESTG00000013893 ENSESTT00000034765 Transcript intron_variant - - - - - - rs161629 17:41059284 C ENSESTG00000013475 ENSESTT00000033733 Transcript intron_variant - - - - - - rs161629 17:41059284 C ENSESTG00000013842 ENSESTT00000034582 Transcript intron_variant - - - - - - rs161629 17:41059284 C 2538 NM_000151.3 Transcript intron_variant - - - - - - rs161629 17:41059284 C 2538 NM_001270397.1 Transcript intron_variant - - - - - - rs161629 17:41059284 C CCDS11446.1 CCDS11446.1 Transcript intron_variant - - - - - - rs161629 17:41059284 C ENSESTG00000013475 ENSESTT00000033736 Transcript intron_variant - - - - - - rs9903972 17:41307485 C ENSESTG00000013737 ENSESTT00000034299 Transcript intron_variant - - - - - - rs9903972 17:41307485 C ENSESTG00000013737 ENSESTT00000034291 Transcript intron_variant - - - - - - rs671502 17:41711084 C - - - intergenic_variant - - - - - - rs394980 17:42111936 C 124801 NM_152344.3 Transcript downstream_gene_variant - - - - - - DISTANCE=67 rs394980 17:42111936 C CCDS11475.1 CCDS11475.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1640 rs394980 17:42111936 C ENSESTG00000001273 ENSESTT00000003013 Transcript downstream_gene_variant - - - - - - DISTANCE=1388 rs2631294 17:42127790 C 124801 NM_152344.3 Transcript intron_variant - - - - - - rs2631294 17:42127790 C CCDS11475.1 CCDS11475.1 Transcript intron_variant - - - - - - rs2631294 17:42127790 C ENSESTG00000001273 ENSESTT00000003013 Transcript intron_variant - - - - - - rs8066661 17:42659005 A - - - intergenic_variant - - - - - - rs8074493 17:43143087 T CCDS11494.1 CCDS11494.1 Transcript intron_variant - - - - - - rs8074493 17:43143087 T 4836 NM_021079.3 Transcript intron_variant - - - - - - rs8074493 17:43143087 T ENSESTG00000001758 ENSESTT00000004342 Transcript upstream_gene_variant - - - - - - DISTANCE=4654 rs8074493 17:43143087 T 79877 NM_024819.4 Transcript upstream_gene_variant - - - - - - DISTANCE=4614 rs8074493 17:43143087 T ENSESTG00000001488 ENSESTT00000003593 Transcript intron_variant - - - - - - rs8074493 17:43143087 T ENSESTG00000001488 ENSESTT00000003590 Transcript intron_variant - - - - - - rs6503429 17:43274260 G - - - intergenic_variant - - - - - - rs4792823 17:43664744 T - - - intergenic_variant - - - - - - rs1358072 17:43739131 G 1394 NM_001256299.1 Transcript intron_variant - - - - - - rs149514869 17:43830356 A 1394 NM_001256299.1 Transcript intron_variant - - - - - - rs143854506 17:43851526 C 1394 NM_001256299.1 Transcript intron_variant - - - - - - rs242952 17:43902580 G CCDS45713.1 CCDS45713.1 Transcript intron_variant - - - - - - rs242952 17:43902580 G 1394 NM_004382.4 Transcript intron_variant - - - - - - rs242952 17:43902580 G ENSESTG00000006816 ENSESTT00000017336 Transcript intron_variant - - - - - - rs242952 17:43902580 G 1394 NM_001145146.1 Transcript intron_variant - - - - - - rs242952 17:43902580 G 1394 NM_001256299.1 Transcript intron_variant - - - - - - rs242952 17:43902580 G CCDS45714.1 CCDS45714.1 Transcript intron_variant - - - - - - rs242952 17:43902580 G CCDS58556.1 CCDS58556.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4971 rs242952 17:43902580 G 1394 NM_001145147.1 Transcript intron_variant - - - - - - rs242952 17:43902580 G CCDS42350.1 CCDS42350.1 Transcript intron_variant - - - - - - rs242952 17:43902580 G 1394 NM_001145148.1 Transcript intron_variant - - - - - - rs242952 17:43902580 G ENSESTG00000006816 ENSESTT00000017340 Transcript intron_variant - - - - - - rs242952 17:43902580 G CCDS45712.1 CCDS45712.1 Transcript intron_variant - - - - - - rs4968276 17:44926412 C ENSESTG00000020972 ENSESTT00000052648 Transcript intron_variant - - - - - - rs4968276 17:44926412 C ENSESTG00000020972 ENSESTT00000052637 Transcript intron_variant - - - - - - rs4968276 17:44926412 C CCDS11506.1 CCDS11506.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2593 rs4968276 17:44926412 C ENSESTG00000020972 ENSESTT00000052669 Transcript upstream_gene_variant - - - - - - DISTANCE=2540 rs4968276 17:44926412 C 7484 NM_003396.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2556 rs1638448 17:44994854 G - - - intergenic_variant - - - - - - rs197924 17:45010436 C ENSESTG00000021000 ENSESTT00000052809 Transcript intron_variant - - - - - - rs197924 17:45010436 C ENSESTG00000021000 ENSESTT00000052787 Transcript downstream_gene_variant - - - - - - DISTANCE=3042 rs197924 17:45010436 C ENSESTG00000021000 ENSESTT00000052775 Transcript downstream_gene_variant - - - - - - DISTANCE=48 rs197924 17:45010436 C ENSESTG00000021000 ENSESTT00000052827 Transcript upstream_gene_variant - - - - - - DISTANCE=1999 rs197924 17:45010436 C 9570 NM_004287.3 Transcript intron_variant - - - - - - rs197924 17:45010436 C 9570 NM_054022.2 Transcript intron_variant - - - - - - rs197924 17:45010436 C CCDS11507.1 CCDS11507.1 Transcript intron_variant - - - - - - rs197924 17:45010436 C 9570 NM_001012511.1 Transcript intron_variant - - - - - - rs197924 17:45010436 C CCDS42355.1 CCDS42355.1 Transcript intron_variant - - - - - - rs197924 17:45010436 C CCDS45719.1 CCDS45719.1 Transcript intron_variant - - - - - - rs3094400 17:45178987 C ENSESTG00000021445 ENSESTT00000053784 Transcript upstream_gene_variant - - - - - - DISTANCE=1697 rs3094400 17:45178987 C ENSESTG00000021445 ENSESTT00000053773 Transcript upstream_gene_variant - - - - - - DISTANCE=1382 rs4346243 17:45748723 C ENSESTG00000022428 ENSESTT00000056935 Transcript intron_variant - - - - - - rs4346243 17:45748723 C ENSESTG00000022428 ENSESTT00000057280 Transcript intron_variant - - - - - - rs4346243 17:45748723 C ENSESTG00000022428 ENSESTT00000057300 Transcript intron_variant - - - - - - rs4346243 17:45748723 C ENSESTG00000022428 ENSESTT00000057303 Transcript intron_variant - - - - - - rs4346243 17:45748723 C ENSESTG00000022428 ENSESTT00000057370 Transcript upstream_gene_variant - - - - - - DISTANCE=3279 rs4346243 17:45748723 C ENSESTG00000022428 ENSESTT00000057355 Transcript upstream_gene_variant - - - - - - DISTANCE=2132 rs4346243 17:45748723 C 3837 NM_002265.4 Transcript intron_variant - - - - - - rs4346243 17:45748723 C ENSESTG00000023741 ENSESTT00000059830 Transcript downstream_gene_variant - - - - - - DISTANCE=3342 rs4346243 17:45748723 C CCDS11513.1 CCDS11513.1 Transcript intron_variant - - - - - - rs4346243 17:45748723 C ENSESTG00000022428 ENSESTT00000057334 Transcript intron_variant - - - - - - rs4346243 17:45748723 C ENSESTG00000022428 ENSESTT00000057315 Transcript intron_variant - - - - - - rs8070379 17:45760349 C ENSESTG00000022428 ENSESTT00000056935 Transcript intron_variant - - - - - - rs8070379 17:45760349 C ENSESTG00000022428 ENSESTT00000057280 Transcript downstream_gene_variant - - - - - - DISTANCE=56 rs8070379 17:45760349 C ENSESTG00000022428 ENSESTT00000057300 Transcript intron_variant - - - - - - rs8070379 17:45760349 C ENSESTG00000022428 ENSESTT00000057303 Transcript downstream_gene_variant - - - - - - DISTANCE=56 rs8070379 17:45760349 C ENSESTG00000022428 ENSESTT00000057370 Transcript downstream_gene_variant - - - - - - DISTANCE=56 rs8070379 17:45760349 C ENSESTG00000022428 ENSESTT00000057355 Transcript downstream_gene_variant - - - - - - DISTANCE=56 rs8070379 17:45760349 C 3837 NM_002265.4 Transcript 3_prime_UTR_variant 3546 - - - - - rs8070379 17:45760349 C ENSESTG00000023741 ENSESTT00000059830 Transcript intron_variant - - - - - - rs8070379 17:45760349 C CCDS11513.1 CCDS11513.1 Transcript downstream_gene_variant - - - - - - DISTANCE=579 rs8070379 17:45760349 C ENSESTG00000022428 ENSESTT00000057334 Transcript downstream_gene_variant - - - - - - DISTANCE=56 rs8070379 17:45760349 C ENSESTG00000022428 ENSESTT00000057315 Transcript downstream_gene_variant - - - - - - DISTANCE=56 rs4793619 17:45803120 C - ENSR00001347962 RegulatoryFeature regulatory_region_variant - - - - - - rs4793619 17:45803120 C - - - intergenic_variant - - - - - - rs208014 17:46253939 G ENSESTG00000023412 ENSESTT00000059177 Transcript intron_variant - - - - - - rs208014 17:46253939 G ENSESTG00000023412 ENSESTT00000059198 Transcript downstream_gene_variant - - - - - - DISTANCE=3643 rs208014 17:46253939 G 8631 NM_003726.3 Transcript intron_variant - - - - - - rs208014 17:46253939 G ENSESTG00000023412 ENSESTT00000059188 Transcript intron_variant - - - - - - rs208014 17:46253939 G 8631 NM_001075099.1 Transcript intron_variant - - - - - - rs208014 17:46253939 G CCDS32674.1 CCDS32674.1 Transcript intron_variant - - - - - - rs4302095 17:46938949 C ENSESTG00000027140 ENSESTT00000068664 Transcript intron_variant - - - - - - rs4302095 17:46938949 C 10241 NM_005831.4 Transcript intron_variant - - - - - - rs4302095 17:46938949 C ENSESTG00000027140 ENSESTT00000068694 Transcript intron_variant - - - - - - rs4302095 17:46938949 C CCDS58559.1 CCDS58559.1 Transcript intron_variant - - - - - - rs4302095 17:46938949 C ENSESTG00000027140 ENSESTT00000068616 Transcript intron_variant - - - - - - rs4302095 17:46938949 C 10241 NM_001261391.1 Transcript intron_variant - - - - - - rs4302095 17:46938949 C ENSESTG00000027140 ENSESTT00000068606 Transcript intron_variant - - - - - - rs4302095 17:46938949 C CCDS58558.1 CCDS58558.1 Transcript intron_variant - - - - - - rs4302095 17:46938949 C 10241 NM_001261390.1 Transcript intron_variant - - - - - - rs4302095 17:46938949 C 10241 NM_001261395.1 Transcript intron_variant - - - - - - rs4302095 17:46938949 C CCDS58561.1 CCDS58561.1 Transcript intron_variant - - - - - - rs4302095 17:46938949 C CCDS11538.1 CCDS11538.1 Transcript intron_variant - - - - - - rs4302095 17:46938949 C ENSESTG00000027140 ENSESTT00000068686 Transcript downstream_gene_variant - - - - - - DISTANCE=1173 rs4302095 17:46938949 C CCDS58560.1 CCDS58560.1 Transcript intron_variant - - - - - - rs4302095 17:46938949 C 10241 NM_001261393.1 Transcript intron_variant - - - - - - rs4793609 17:47231233 G 124872 NM_001159387.1 Transcript intron_variant - - - - - - rs4793609 17:47231233 G 124872 NM_153446.2 Transcript intron_variant - - - - - - rs4793609 17:47231233 G ENSESTG00000027519 ENSESTT00000069285 Transcript intron_variant - - - - - - rs4793609 17:47231233 G CCDS11544.1 CCDS11544.1 Transcript intron_variant - - - - - - rs4793609 17:47231233 G 124872 NM_001159388.1 Transcript intron_variant - - - - - - rs4793609 17:47231233 G CCDS54140.1 CCDS54140.1 Transcript intron_variant - - - - - - rs4793609 17:47231233 G CCDS54139.1 CCDS54139.1 Transcript intron_variant - - - - - - rs8070296 17:47235858 G 124872 NM_001159387.1 Transcript intron_variant - - - - - - rs8070296 17:47235858 G 124872 NM_153446.2 Transcript intron_variant - - - - - - rs8070296 17:47235858 G ENSESTG00000027519 ENSESTT00000069285 Transcript intron_variant - - - - - - rs8070296 17:47235858 G CCDS11544.1 CCDS11544.1 Transcript intron_variant - - - - - - rs8070296 17:47235858 G 124872 NM_001159388.1 Transcript intron_variant - - - - - - rs8070296 17:47235858 G CCDS54140.1 CCDS54140.1 Transcript intron_variant - - - - - - rs8070296 17:47235858 G CCDS54139.1 CCDS54139.1 Transcript intron_variant - - - - - - rs1523137 17:47237802 G 124872 NM_001159387.1 Transcript intron_variant - - - - - - rs1523137 17:47237802 G 124872 NM_153446.2 Transcript intron_variant - - - - - - rs1523137 17:47237802 G ENSESTG00000027519 ENSESTT00000069285 Transcript intron_variant - - - - - - rs1523137 17:47237802 G CCDS11544.1 CCDS11544.1 Transcript intron_variant - - - - - - rs1523137 17:47237802 G 124872 NM_001159388.1 Transcript intron_variant - - - - - - rs1523137 17:47237802 G CCDS54140.1 CCDS54140.1 Transcript intron_variant - - - - - - rs1523137 17:47237802 G CCDS54139.1 CCDS54139.1 Transcript intron_variant - - - - - - rs2537699 17:47678578 C - ENSR00001348502 RegulatoryFeature regulatory_region_variant - - - - - - rs2537699 17:47678578 C 8405 NM_001007228.1 Transcript intron_variant - - - - - - rs2537699 17:47678578 C ENSESTG00000005961 ENSESTT00000015191 Transcript intron_variant - - - - - - rs2537699 17:47678578 C ENSESTG00000005961 ENSESTT00000015160 Transcript intron_variant - - - - - - rs2537699 17:47678578 C ENSESTG00000005961 ENSESTT00000015196 Transcript intron_variant - - - - - - rs2537699 17:47678578 C 8405 NM_001007226.1 Transcript intron_variant - - - - - - rs2537699 17:47678578 C 8405 NM_003563.3 Transcript intron_variant - - - - - - rs2537699 17:47678578 C 8405 NM_001007227.1 Transcript intron_variant - - - - - - rs2537699 17:47678578 C 8405 NM_001007229.1 Transcript intron_variant - - - - - - rs2537699 17:47678578 C 8405 NM_001007230.1 Transcript intron_variant - - - - - - rs2537699 17:47678578 C ENSESTG00000005961 ENSESTT00000015166 Transcript intron_variant - - - - - - rs2537699 17:47678578 C CCDS11551.1 CCDS11551.1 Transcript intron_variant - - - - - - rs2537699 17:47678578 C ENSESTG00000005961 ENSESTT00000015208 Transcript intron_variant - - - - - - rs271660 17:48017302 A - - - intergenic_variant - - - - - - rs1858902 17:48155909 T - ENSR00001348643 RegulatoryFeature regulatory_region_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014678 Transcript intron_variant - - - - - - rs1858902 17:48155909 T CCDS11558.1 CCDS11558.1 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014675 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000006266 ENSESTT00000015793 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014703 Transcript downstream_gene_variant - - - - - - DISTANCE=4074 rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014676 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014649 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014711 Transcript downstream_gene_variant - - - - - - DISTANCE=1812 rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014656 Transcript intron_variant - - - - - - rs1858902 17:48155909 T 3675 NM_005501.2 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014640 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014629 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014670 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014679 Transcript downstream_gene_variant - - - - - - DISTANCE=4074 rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014700 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014681 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014694 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014646 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014654 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014718 Transcript upstream_gene_variant - - - - - - DISTANCE=1772 rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014685 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014689 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014677 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014691 Transcript intron_variant - - - - - - rs1858902 17:48155909 T CCDS11557.1 CCDS11557.1 Transcript intron_variant - - - - - - rs1858902 17:48155909 T ENSESTG00000005743 ENSESTT00000014668 Transcript intron_variant - - - - - - rs1858902 17:48155909 T 3675 NM_002204.2 Transcript intron_variant - - - - - - rs2696277 17:48292050 C ENSESTG00000005878 ENSESTT00000014904 Transcript upstream_gene_variant - - - - - - DISTANCE=21 rs2586443 17:48312710 G - - - intergenic_variant - - - - - - rs7222994 17:48381723 C - - - intergenic_variant - - - - - - rs4794177 17:48748176 G ENSESTG00000016993 ENSESTT00000042709 Transcript intron_variant - - - - - - rs4794177 17:48748176 G ENSESTG00000016993 ENSESTT00000042742 Transcript intron_variant - - - - - - rs4794177 17:48748176 G CCDS45739.1 CCDS45739.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2974 rs4794177 17:48748176 G ENSESTG00000016948 ENSESTT00000042596 Transcript downstream_gene_variant - - - - - - DISTANCE=2892 rs4794177 17:48748176 G ENSESTG00000016993 ENSESTT00000042759 Transcript intron_variant - - - - - - rs4794177 17:48748176 G 8714 NM_003786.3 Transcript intron_variant - - - - - - rs4794177 17:48748176 G 8714 NM_001144070.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2888 rs4794177 17:48748176 G ENSESTG00000016948 ENSESTT00000042604 Transcript downstream_gene_variant - - - - - - DISTANCE=2892 rs4794177 17:48748176 G ENSESTG00000016948 ENSESTT00000042616 Transcript downstream_gene_variant - - - - - - DISTANCE=2897 rs4794177 17:48748176 G CCDS32681.1 CCDS32681.1 Transcript intron_variant - - - - - - rs6504679 17:48811576 C 51747 NM_006107.3 Transcript intron_variant - - - - - - rs6504679 17:48811576 C ENSESTG00000017063 ENSESTT00000042980 Transcript intron_variant - - - - - - rs6504679 17:48811576 C ENSESTG00000017063 ENSESTT00000042959 Transcript intron_variant - - - - - - rs6504679 17:48811576 C CCDS11573.1 CCDS11573.1 Transcript intron_variant - - - - - - rs6504679 17:48811576 C ENSESTG00000017063 ENSESTT00000042971 Transcript intron_variant - - - - - - rs6504679 17:48811576 C 51747 NM_016424.4 Transcript intron_variant - - - - - - rs6504681 17:48813588 G 51747 NM_006107.3 Transcript intron_variant - - - - - - rs6504681 17:48813588 G ENSESTG00000017063 ENSESTT00000042980 Transcript intron_variant - - - - - - rs6504681 17:48813588 G ENSESTG00000017063 ENSESTT00000042959 Transcript intron_variant - - - - - - rs6504681 17:48813588 G CCDS11573.1 CCDS11573.1 Transcript intron_variant - - - - - - rs6504681 17:48813588 G ENSESTG00000017063 ENSESTT00000042971 Transcript intron_variant - - - - - - rs6504681 17:48813588 G 51747 NM_016424.4 Transcript intron_variant - - - - - - rs4794290 17:49737548 G ENSESTG00000032568 ENSESTT00000082276 Transcript intron_variant - - - - - - rs4794290 17:49737548 G ENSESTG00000032568 ENSESTT00000082290 Transcript downstream_gene_variant - - - - - - DISTANCE=1410 rs4794290 17:49737548 G ENSESTG00000032568 ENSESTT00000082282 Transcript intron_variant - - - - - - rs4794290 17:49737548 G 56934 NM_020178.4 Transcript intron_variant - - - - - - rs4794290 17:49737548 G 56934 NM_001082534.1 Transcript intron_variant - - - - - - rs4794290 17:49737548 G 56934 NM_001082533.1 Transcript intron_variant - - - - - - rs4794290 17:49737548 G CCDS32684.1 CCDS32684.1 Transcript intron_variant - - - - - - rs202139 17:49944643 T ENSESTG00000032568 ENSESTT00000082276 Transcript intron_variant - - - - - - rs202139 17:49944643 T 56934 NM_020178.4 Transcript intron_variant - - - - - - rs202139 17:49944643 T 56934 NM_001082534.1 Transcript intron_variant - - - - - - rs202139 17:49944643 T 56934 NM_001082533.1 Transcript intron_variant - - - - - - rs202139 17:49944643 T CCDS32684.1 CCDS32684.1 Transcript intron_variant - - - - - - rs4793735 17:50156185 C ENSESTG00000032568 ENSESTT00000082276 Transcript intron_variant - - - - - - rs4793735 17:50156185 C 56934 NM_020178.4 Transcript intron_variant - - - - - - rs4793735 17:50156185 C 56934 NM_001082534.1 Transcript intron_variant - - - - - - rs4793735 17:50156185 C 56934 NM_001082533.1 Transcript intron_variant - - - - - - rs4793735 17:50156185 C CCDS32684.1 CCDS32684.1 Transcript intron_variant - - - - - - rs4368200 17:50166488 G ENSESTG00000032568 ENSESTT00000082276 Transcript intron_variant - - - - - - rs4368200 17:50166488 G 56934 NM_020178.4 Transcript intron_variant - - - - - - rs4368200 17:50166488 G 56934 NM_001082534.1 Transcript intron_variant - - - - - - rs4368200 17:50166488 G 56934 NM_001082533.1 Transcript intron_variant - - - - - - rs4368200 17:50166488 G CCDS32684.1 CCDS32684.1 Transcript intron_variant - - - - - - rs349991 17:50622038 G - - - intergenic_variant - - - - - - rs12936136 17:50819655 C - - - intergenic_variant - - - - - - rs9890994 17:50830325 G - - - intergenic_variant - - - - - - rs806883 17:51422265 T - - - intergenic_variant - - - - - - rs4344795 17:51534613 T - - - intergenic_variant - - - - - - rs4359492 17:51589644 A - - - intergenic_variant - - - - - - rs1179362 17:52276436 T - - - intergenic_variant - - - - - - rs7207576 17:52824393 C - - - intergenic_variant - - - - - - rs2958868 17:52918215 T - - - intergenic_variant - - - - - - rs2958909 17:53001954 T ENSESTG00000033032 ENSESTT00000083634 Transcript intron_variant - - - - - - rs2958909 17:53001954 T CCDS11582.1 CCDS11582.1 Transcript intron_variant - - - - - - rs2958909 17:53001954 T ENSESTG00000033167 ENSESTT00000083838 Transcript intron_variant - - - - - - rs2958909 17:53001954 T ENSESTG00000033032 ENSESTT00000083638 Transcript intron_variant - - - - - - rs2958909 17:53001954 T ENSESTG00000033032 ENSESTT00000083656 Transcript intron_variant - - - - - - rs2958909 17:53001954 T 10040 NM_005486.2 Transcript intron_variant - - - - - - rs2958909 17:53001954 T ENSESTG00000033032 ENSESTT00000083651 Transcript intron_variant - - - - - - rs244327 17:53269948 T - - - intergenic_variant - - - - - - rs244388 17:53308822 C - - - intergenic_variant - - - - - - rs8076608 17:53731761 T - - - intergenic_variant - - - - - - rs1454111 17:53998212 G - - - intergenic_variant - - - - - - rs975836 17:54001764 G - - - intergenic_variant - - - - - - rs920692 17:54607463 A - - - intergenic_variant - - - - - - rs9915976 17:54674011 T - ENSR00001349460 RegulatoryFeature regulatory_region_variant - - - - - - rs9915976 17:54674011 T CCDS11589.1 CCDS11589.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1728 rs9915976 17:54674011 T 9241 NM_005450.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1060 rs1867163 17:54689911 T - - - intergenic_variant - - - - - - rs4517850 17:54704955 G - - - intergenic_variant - - - - - - rs7224584 17:54736372 G - - - intergenic_variant - - - - - - rs227668 17:54797147 G - - - intergenic_variant - - - - - - rs4794710 17:55297161 C - - - intergenic_variant - - - - - - rs1017089 17:56544280 G ENSESTG00000019077 ENSESTT00000048008 Transcript missense_variant 1098 986 329 N/T aAt/aCt - rs1017089 17:56544280 G 124535 NM_001080439.1 Transcript missense_variant 1110 986 329 N/T aAt/aCt - PolyPhen=benign;SIFT=tolerated rs1017089 17:56544280 G ENSESTG00000019077 ENSESTT00000048021 Transcript missense_variant 860 860 287 N/T aAt/aCt - rs1017089 17:56544280 G CCDS32690.1 CCDS32690.1 Transcript missense_variant 986 986 329 N/T aAt/aCt - PolyPhen=benign;SIFT=tolerated rs1017089 17:56544280 G ENSESTG00000019102 ENSESTT00000048054 Transcript upstream_gene_variant - - - - - - DISTANCE=3807 rs304294 17:56823057 C - - - intergenic_variant - - - - - - rs8074595 17:57111654 A CCDS32694.1 CCDS32694.1 Transcript intron_variant - - - - - - rs8074595 17:57111654 A ENSESTG00000018626 ENSESTT00000047303 Transcript intron_variant - - - - - - rs8074595 17:57111654 A CCDS45746.1 CCDS45746.1 Transcript intron_variant - - - - - - rs8074595 17:57111654 A ENSESTG00000018626 ENSESTT00000047300 Transcript intron_variant - - - - - - rs8074595 17:57111654 A ENSESTG00000018626 ENSESTT00000047276 Transcript intron_variant - - - - - - rs8074595 17:57111654 A ENSESTG00000018626 ENSESTT00000047269 Transcript intron_variant - - - - - - rs8074595 17:57111654 A 4591 NM_015294.3 Transcript intron_variant - - - - - - rs8074595 17:57111654 A ENSESTG00000018626 ENSESTT00000047297 Transcript intron_variant - - - - - - rs8074595 17:57111654 A ENSESTG00000018626 ENSESTT00000047257 Transcript intron_variant - - - - - - rs8074595 17:57111654 A 4591 NM_001005207.2 Transcript intron_variant - - - - - - rs8074595 17:57111654 A ENSESTG00000018626 ENSESTT00000047263 Transcript intron_variant - - - - - - rs8074595 17:57111654 A ENSESTG00000018626 ENSESTT00000047328 Transcript intron_variant - - - - - - rs8074595 17:57111654 A ENSESTG00000018626 ENSESTT00000047307 Transcript intron_variant - - - - - - rs6503917 17:57480449 G 388403 NM_001005404.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1354 rs4968399 17:57941451 A 51174 NM_001193613.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A ENSESTG00000032399 ENSESTT00000081858 Transcript intron_variant - - - - - - rs4968399 17:57941451 A CCDS54153.1 CCDS54153.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A ENSESTG00000032399 ENSESTT00000081870 Transcript intron_variant - - - - - - rs4968399 17:57941451 A 51174 NM_001193612.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A 51174 NM_001193609.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A CCDS54152.1 CCDS54152.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A ENSESTG00000032399 ENSESTT00000081853 Transcript intron_variant - - - - - - rs4968399 17:57941451 A 51174 NM_001193611.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A CCDS11620.1 CCDS11620.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A 51174 NM_016261.3 Transcript intron_variant - - - - - - rs4968399 17:57941451 A ENSESTG00000032399 ENSESTT00000081883 Transcript intron_variant - - - - - - rs4968399 17:57941451 A CCDS54154.1 CCDS54154.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A CCDS54151.1 CCDS54151.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A 51174 NM_001193610.1 Transcript intron_variant - - - - - - rs4968399 17:57941451 A ENSESTG00000032399 ENSESTT00000081878 Transcript intron_variant - - - - - - rs61567769 17:58052491 C ENSESTG00000032275 ENSESTT00000081636 Transcript intron_variant - - - - - - rs61567769 17:58052491 C ENSESTG00000032275 ENSESTT00000081653 Transcript downstream_gene_variant - - - - - - DISTANCE=710 rs61567769 17:58052491 C 653645 NR_002924.2 Transcript downstream_gene_variant - - - - - - DISTANCE=894 rs2627908 17:58218764 A - - - intergenic_variant - - - - - - rs8071051 17:58524194 A CCDS32699.1 CCDS32699.1 Transcript downstream_gene_variant - - - - - - DISTANCE=748 rs8071051 17:58524194 A 10513 NM_006380.2 Transcript 3_prime_UTR_variant 2794 - - - - - rs4559964 17:58875632 T ENSESTG00000030334 ENSESTT00000076554 Transcript intron_variant - - - - - - rs4559964 17:58875632 T ENSESTG00000030334 ENSESTT00000076385 Transcript intron_variant - - - - - - rs4559964 17:58875632 T 54828 NM_001099432.1 Transcript intron_variant - - - - - - rs4559964 17:58875632 T ENSESTG00000030334 ENSESTT00000076502 Transcript intron_variant - - - - - - rs4559964 17:58875632 T CCDS45749.1 CCDS45749.1 Transcript intron_variant - - - - - - rs4559964 17:58875632 T 54828 NM_017679.3 Transcript intron_variant - - - - - - rs4559964 17:58875632 T CCDS11626.1 CCDS11626.1 Transcript intron_variant - - - - - - rs6504004 17:58951161 A ENSESTG00000030334 ENSESTT00000076554 Transcript intron_variant - - - - - - rs6504004 17:58951161 A 54828 NM_001099432.1 Transcript intron_variant - - - - - - rs6504004 17:58951161 A ENSESTG00000030334 ENSESTT00000076502 Transcript intron_variant - - - - - - rs6504004 17:58951161 A CCDS45749.1 CCDS45749.1 Transcript intron_variant - - - - - - rs6504004 17:58951161 A 54828 NM_017679.3 Transcript intron_variant - - - - - - rs6504004 17:58951161 A CCDS11626.1 CCDS11626.1 Transcript intron_variant - - - - - - rs8074852 17:59171605 G 54828 NM_001099432.1 Transcript intron_variant - - - - - - rs8074852 17:59171605 G CCDS45749.1 CCDS45749.1 Transcript intron_variant - - - - - - rs8074852 17:59171605 G 54828 NM_017679.3 Transcript intron_variant - - - - - - rs8074852 17:59171605 G CCDS11626.1 CCDS11626.1 Transcript intron_variant - - - - - - rs4419113 17:59213634 C 54828 NM_001099432.1 Transcript intron_variant - - - - - - rs4419113 17:59213634 C CCDS45749.1 CCDS45749.1 Transcript intron_variant - - - - - - rs4419113 17:59213634 C 54828 NM_017679.3 Transcript intron_variant - - - - - - rs4419113 17:59213634 C CCDS11626.1 CCDS11626.1 Transcript intron_variant - - - - - - rs4968541 17:59317750 G 54828 NM_001099432.1 Transcript intron_variant - - - - - - rs4968541 17:59317750 G CCDS45749.1 CCDS45749.1 Transcript intron_variant - - - - - - rs4968541 17:59317750 G 54828 NM_017679.3 Transcript intron_variant - - - - - - rs4968541 17:59317750 G ENSESTG00000030484 ENSESTT00000076765 Transcript intron_variant - - - - - - rs4968541 17:59317750 G CCDS11626.1 CCDS11626.1 Transcript intron_variant - - - - - - rs9906297 17:59327866 A - ENSR00001350470 RegulatoryFeature regulatory_region_variant - - - - - - rs9906297 17:59327866 A 54828 NM_001099432.1 Transcript intron_variant - - - - - - rs9906297 17:59327866 A ENSESTG00000030484 ENSESTT00000076772 Transcript upstream_gene_variant - - - - - - DISTANCE=4571 rs9906297 17:59327866 A CCDS45749.1 CCDS45749.1 Transcript intron_variant - - - - - - rs9906297 17:59327866 A 54828 NM_017679.3 Transcript intron_variant - - - - - - rs9906297 17:59327866 A ENSESTG00000030484 ENSESTT00000076765 Transcript intron_variant - - - - - - rs9906297 17:59327866 A CCDS11626.1 CCDS11626.1 Transcript intron_variant - - - - - - rs680696 17:59982693 C ENSESTG00000031750 ENSESTT00000080212 Transcript intron_variant - - - - - - rs680696 17:59982693 C CCDS45750.1 CCDS45750.1 Transcript intron_variant - - - - - - rs680696 17:59982693 C 57508 NM_020748.2 Transcript intron_variant - - - - - - rs680696 17:59982693 C ENSESTG00000031750 ENSESTT00000080243 Transcript intron_variant - - - - - - rs680696 17:59982693 C 57508 NR_026641.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7222729 17:60138409 C ENSESTG00000031583 ENSESTT00000079741 Transcript intron_variant - - - - - - rs7222729 17:60138409 C ENSESTG00000031583 ENSESTT00000079630 Transcript intron_variant - - - - - - rs7222729 17:60138409 C ENSESTG00000031583 ENSESTT00000079677 Transcript intron_variant - - - - - - rs7222729 17:60138409 C CCDS42366.1 CCDS42366.1 Transcript intron_variant - - - - - - rs7222729 17:60138409 C 9969 NM_005121.2 Transcript intron_variant - - - - - - rs12709414 17:60323537 G - - - intergenic_variant - - - - - - rs4968421 17:60399658 G - - - intergenic_variant - - - - - - rs11871373 17:60788106 G ENSESTG00000009344 ENSESTT00000023418 Transcript intron_variant - - - - - - rs11871373 17:60788106 G 162333 NM_152598.2 Transcript intron_variant - - - - - - rs11871373 17:60788106 G ENSESTG00000009344 ENSESTT00000023415 Transcript intron_variant - - - - - - rs11871373 17:60788106 G ENSESTG00000009306 ENSESTT00000023318 Transcript intron_variant - - - - - - rs11871373 17:60788106 G ENSESTG00000009306 ENSESTT00000023313 Transcript intron_variant - - - - - - rs11871373 17:60788106 G 162333 NM_001100875.1 Transcript intron_variant - - - - - - rs11871373 17:60788106 G CCDS11635.1 CCDS11635.1 Transcript intron_variant - - - - - - rs4644910 17:60839442 A - ENSR00001350764 RegulatoryFeature regulatory_region_variant - - - - - - rs4644910 17:60839442 A 162333 NM_152598.2 Transcript intron_variant - - - - - - rs4644910 17:60839442 A 162333 NM_001100875.1 Transcript intron_variant - - - - - - rs4644910 17:60839442 A ENSESTG00000009328 ENSESTT00000023399 Transcript intron_variant - - - - - - rs4644910 17:60839442 A ENSESTG00000009328 ENSESTT00000023392 Transcript intron_variant - - - - - - rs4644910 17:60839442 A CCDS11635.1 CCDS11635.1 Transcript intron_variant - - - - - - rs7503425 17:61658951 G ENSESTG00000007658 ENSESTT00000019321 Transcript downstream_gene_variant - - - - - - DISTANCE=2137 rs7503425 17:61658951 G ENSESTG00000008810 ENSESTT00000022118 Transcript intron_variant - - - - - - rs7503425 17:61658951 G ENSESTG00000007658 ENSESTT00000019317 Transcript intron_variant - - - - - - rs7503425 17:61658951 G 10238 NM_005828.3 Transcript intron_variant - - - - - - rs7503425 17:61658951 G ENSESTG00000007678 ENSESTT00000019343 Transcript upstream_gene_variant - - - - - - DISTANCE=3667 rs967273 17:62071438 A CCDS54159.1 CCDS54159.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4287 rs967273 17:62071438 A CCDS54157.1 CCDS54157.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4287 rs967273 17:62071438 A 92340 NM_001191029.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4273 rs967273 17:62071438 A 92340 NM_001191031.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4273 rs967273 17:62071438 A ENSESTG00000007900 ENSESTT00000019964 Transcript upstream_gene_variant - - - - - - DISTANCE=4273 rs967273 17:62071438 A CCDS54158.1 CCDS54158.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4287 rs967273 17:62071438 A ENSESTG00000007900 ENSESTT00000019966 Transcript upstream_gene_variant - - - - - - DISTANCE=4273 rs967273 17:62071438 A 92340 NM_001191030.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4273 rs967273 17:62071438 A 92340 NM_001164257.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4273 rs967273 17:62071438 A CCDS58586.1 CCDS58586.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4287 rs1967130 17:62254983 A - ENSR00001351111 RegulatoryFeature regulatory_region_variant - - - - - - rs1967130 17:62254983 A CCDS11658.1 CCDS11658.1 Transcript intron_variant - - - - - - rs1967130 17:62254983 A ENSESTG00000008166 ENSESTT00000020708 Transcript intron_variant - - - - - - rs1967130 17:62254983 A 55852 NM_018469.3 Transcript intron_variant - - - - - - rs1967130 17:62254983 A ENSESTG00000008166 ENSESTT00000020726 Transcript intron_variant - - - - - - rs7209104 17:62613153 C ENSESTG00000024250 ENSESTT00000061696 Transcript intron_variant - - - - - - rs7209104 17:62613153 C ENSESTG00000024250 ENSESTT00000061670 Transcript intron_variant - - - - - - rs7209104 17:62613153 C ENSESTG00000024250 ENSESTT00000061637 Transcript intron_variant - - - - - - rs7209104 17:62613153 C CCDS32707.1 CCDS32707.1 Transcript intron_variant - - - - - - rs7209104 17:62613153 C ENSESTG00000024250 ENSESTT00000061691 Transcript intron_variant - - - - - - rs7209104 17:62613153 C 64750 NM_022739.3 Transcript intron_variant - - - - - - rs6504255 17:62782689 C - ENSR00001351168 RegulatoryFeature regulatory_region_variant - - - - - - rs6504255 17:62782689 C 440456 NR_024386.1 Transcript non_coding_exon_variant,nc_transcript_variant 2391 - - - - - rs6504255 17:62782689 C ENSESTG00000023935 ENSESTT00000060674 Transcript downstream_gene_variant - - - - - - DISTANCE=65 rs6504255 17:62782689 C 146880 NR_026899.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4572 rs6504255 17:62782689 C ENSESTG00000023935 ENSESTT00000060663 Transcript downstream_gene_variant - - - - - - DISTANCE=65 rs6504255 17:62782689 C ENSESTG00000023935 ENSESTT00000060660 Transcript missense_variant 2047 1480 494 I/V Atc/Gtc - rs6504255 17:62782689 C ENSESTG00000023321 ENSESTT00000058849 Transcript downstream_gene_variant - - - - - - DISTANCE=3878 rs6504255 17:62782689 C ENSESTG00000023935 ENSESTT00000060528 Transcript missense_variant 2380 1480 494 I/V Atc/Gtc - rs6504255 17:62782689 C ENSESTG00000023935 ENSESTT00000060670 Transcript missense_variant 2073 1480 494 I/V Atc/Gtc - rs6504255 17:62782689 C ENSESTG00000023935 ENSESTT00000060544 Transcript downstream_gene_variant - - - - - - DISTANCE=65 rs6504255 17:62782689 C ENSESTG00000023935 ENSESTT00000060616 Transcript missense_variant 2362 1480 494 I/V Atc/Gtc - rs6504255 17:62782689 C ENSESTG00000023935 ENSESTT00000060635 Transcript downstream_gene_variant - - - - - - DISTANCE=65 rs4791229 17:63166357 G 8787 NM_003835.3 Transcript intron_variant - - - - - - rs4791229 17:63166357 G CCDS42373.1 CCDS42373.1 Transcript intron_variant - - - - - - rs4791229 17:63166357 G 8787 NM_001165933.1 Transcript intron_variant - - - - - - rs4791229 17:63166357 G ENSESTG00000023429 ENSESTT00000059396 Transcript intron_variant - - - - - - rs4791229 17:63166357 G CCDS45764.1 CCDS45764.1 Transcript intron_variant - - - - - - rs4791229 17:63166357 G 8787 NM_001081955.2 Transcript intron_variant - - - - - - rs9907018 17:63208534 G 8787 NM_003835.3 Transcript intron_variant - - - - - - rs9907018 17:63208534 G CCDS42373.1 CCDS42373.1 Transcript intron_variant - - - - - - rs9907018 17:63208534 G 8787 NM_001165933.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1754 rs9907018 17:63208534 G ENSESTG00000023429 ENSESTT00000059396 Transcript intron_variant - - - - - - rs9907018 17:63208534 G CCDS45764.1 CCDS45764.1 Transcript intron_variant - - - - - - rs9907018 17:63208534 G 8787 NM_001081955.2 Transcript intron_variant - - - - - - rs1234195 17:63236172 G - - - intergenic_variant - - - - - - rs9897394 17:63286996 G - - - intergenic_variant - - - - - - rs4791182 17:63500017 G ENSESTG00000033976 ENSESTT00000085869 Transcript missense_variant 439 304 102 H/D Cat/Gat - rs11079608 17:63946869 G 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs11079608 17:63946869 G ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs11079608 17:63946869 G CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs11079608 17:63946869 G 201134 NM_145036.3 Transcript intron_variant - - - - - - rs11079608 17:63946869 G ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs10853066 17:63962483 G - ENSR00001351408 RegulatoryFeature regulatory_region_variant - - - - - - rs10853066 17:63962483 G 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs10853066 17:63962483 G ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs10853066 17:63962483 G CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs10853066 17:63962483 G 201134 NM_145036.3 Transcript intron_variant - - - - - - rs10853066 17:63962483 G ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs7222587 17:63995820 T 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs7222587 17:63995820 T ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs7222587 17:63995820 T CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs7222587 17:63995820 T 201134 NM_145036.3 Transcript intron_variant - - - - - - rs7222587 17:63995820 T ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs1443286 17:64020235 A 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs1443286 17:64020235 A ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs1443286 17:64020235 A CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs1443286 17:64020235 A 201134 NM_145036.3 Transcript intron_variant - - - - - - rs1443286 17:64020235 A ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs9914168 17:64022767 G 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs9914168 17:64022767 G ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs9914168 17:64022767 G CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs9914168 17:64022767 G 201134 NM_145036.3 Transcript intron_variant - - - - - - rs9914168 17:64022767 G ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs2056235 17:64043581 T 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs2056235 17:64043581 T ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs2056235 17:64043581 T CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs2056235 17:64043581 T 201134 NM_145036.3 Transcript intron_variant - - - - - - rs2056235 17:64043581 T ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs11079639 17:64060363 C 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs11079639 17:64060363 C ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs11079639 17:64060363 C CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs11079639 17:64060363 C 201134 NM_145036.3 Transcript intron_variant - - - - - - rs11079639 17:64060363 C ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs1899582 17:64071247 A 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs1899582 17:64071247 A ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs1899582 17:64071247 A CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs1899582 17:64071247 A 201134 NM_145036.3 Transcript intron_variant - - - - - - rs1899582 17:64071247 A ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs7210759 17:64102772 A 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs7210759 17:64102772 A ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs7210759 17:64102772 A CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs7210759 17:64102772 A 201134 NM_145036.3 Transcript intron_variant - - - - - - rs7210759 17:64102772 A ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs230565 17:64165303 T 201134 NM_001199165.1 Transcript intron_variant - - - - - - rs230565 17:64165303 T ENSESTG00000034029 ENSESTT00000086092 Transcript intron_variant - - - - - - rs230565 17:64165303 T CCDS32710.1 CCDS32710.1 Transcript intron_variant - - - - - - rs230565 17:64165303 T 201134 NM_145036.3 Transcript intron_variant - - - - - - rs230565 17:64165303 T ENSESTG00000034029 ENSESTT00000086079 Transcript intron_variant - - - - - - rs4791071 17:64316173 A ENSESTG00000033980 ENSESTT00000085902 Transcript intron_variant - - - - - - rs4791071 17:64316173 A CCDS11664.1 CCDS11664.1 Transcript intron_variant - - - - - - rs4791071 17:64316173 A 5578 NM_002737.2 Transcript intron_variant - - - - - - rs2248274 17:64491298 A ENSESTG00000033980 ENSESTT00000085902 Transcript intron_variant - - - - - - rs2248274 17:64491298 A ENSESTG00000019136 ENSESTT00000048234 Transcript upstream_gene_variant - - - - - - DISTANCE=1021 rs2248274 17:64491298 A CCDS11664.1 CCDS11664.1 Transcript intron_variant - - - - - - rs2248274 17:64491298 A 5578 NM_002737.2 Transcript intron_variant - - - - - - rs1990343 17:64848403 C ENSESTG00000019206 ENSESTT00000048287 Transcript intron_variant - - - - - - rs2706697 17:65610297 C CCDS58587.1 CCDS58587.1 Transcript intron_variant - - - - - - rs2706697 17:65610297 C ENSESTG00000002370 ENSESTT00000005912 Transcript intron_variant - - - - - - rs2706697 17:65610297 C 26207 NM_181671.2 Transcript intron_variant - - - - - - rs2706697 17:65610297 C ENSESTG00000002370 ENSESTT00000005887 Transcript intron_variant - - - - - - rs2706697 17:65610297 C CCDS58588.1 CCDS58588.1 Transcript intron_variant - - - - - - rs2706697 17:65610297 C ENSESTG00000002370 ENSESTT00000005874 Transcript intron_variant - - - - - - rs2706697 17:65610297 C 26207 NM_012417.3 Transcript intron_variant - - - - - - rs7218206 17:65712401 T - ENSR00001351774 RegulatoryFeature regulatory_region_variant - - - - - - rs7218206 17:65712401 T CCDS11671.1 CCDS11671.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1663 rs7218206 17:65712401 T ENSESTG00000002387 ENSESTT00000005980 Transcript upstream_gene_variant - - - - - - DISTANCE=1650 rs7218206 17:65712401 T 25926 NM_015462.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1660 rs7218206 17:65712401 T ENSESTG00000002641 ENSESTT00000006557 Transcript intron_variant - - - - - - rs4791301 17:65921984 A - ENSR00001351816 RegulatoryFeature regulatory_region_variant - - - - - - rs4791301 17:65921984 A ENSESTG00000002476 ENSESTT00000006155 Transcript intron_variant - - - - - - rs4791301 17:65921984 A 2186 NM_004459.6 Transcript intron_variant - - - - - - rs4791301 17:65921984 A ENSESTG00000002476 ENSESTT00000006162 Transcript intron_variant - - - - - - rs4791301 17:65921984 A ENSESTG00000002476 ENSESTT00000006166 Transcript intron_variant - - - - - - rs4791301 17:65921984 A 2186 NM_182641.3 Transcript intron_variant - - - - - - rs4791301 17:65921984 A CCDS11672.1 CCDS11672.1 Transcript intron_variant - - - - - - rs4791301 17:65921984 A CCDS11673.1 CCDS11673.1 Transcript intron_variant - - - - - - rs4968925 17:66676584 G ENSESTG00000007388 ENSESTT00000018585 Transcript downstream_gene_variant - - - - - - DISTANCE=3277 rs7212957 17:67241324 A ENSESTG00000007418 ENSESTT00000018810 Transcript downstream_gene_variant - - - - - - DISTANCE=2160 rs7212957 17:67241324 A ENSESTG00000007418 ENSESTT00000018789 Transcript downstream_gene_variant - - - - - - DISTANCE=2160 rs7212957 17:67241324 A ENSESTG00000007418 ENSESTT00000018760 Transcript downstream_gene_variant - - - - - - DISTANCE=2160 rs7212957 17:67241324 A CCDS11685.1 CCDS11685.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2354 rs7212957 17:67241324 A 10349 NM_080282.3 Transcript upstream_gene_variant - - - - - - DISTANCE=368 rs7212957 17:67241324 A ENSESTG00000007418 ENSESTT00000018827 Transcript downstream_gene_variant - - - - - - DISTANCE=2160 rs7212957 17:67241324 A 23461 NM_018672.3 Transcript 3_prime_UTR_variant 8501 - - - - - rs7212957 17:67241324 A 23461 NM_172232.2 Transcript 3_prime_UTR_variant 7429 - - - - - rs2188698 17:67687213 G - - - intergenic_variant - - - - - - rs756929 17:67816180 C - ENSR00001537766 RegulatoryFeature regulatory_region_variant - - - - - - rs756929 17:67816180 C ENSESTG00000002264 ENSESTT00000005644 Transcript intron_variant - - - - - - rs420132 17:68335223 C - ENSR00001352291 RegulatoryFeature regulatory_region_variant - - - - - - rs420132 17:68335223 C ENSESTG00000002296 ENSESTT00000005719 Transcript intron_variant - - - - - - rs2079748 17:68714445 C - - - intergenic_variant - - - - - - rs1154955 17:68731248 A - - - intergenic_variant - - - - - - rs2216286 17:69031406 C - - - intergenic_variant - - - - - - rs1861688 17:69059038 C - - - intergenic_variant - - - - - - rs917279 17:69221939 C - - - intergenic_variant - - - - - - rs2341346 17:69864812 G - - - intergenic_variant - - - - - - rs7222382 17:70625131 C 400619 NR_033876.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6501588 17:70989806 A 201266 NM_139177.3 Transcript intron_variant - - - - - - rs6501588 17:70989806 A 201266 NM_001159770.1 Transcript intron_variant - - - - - - rs6501588 17:70989806 A ENSESTG00000000781 ENSESTT00000001912 Transcript intron_variant - - - - - - rs6501588 17:70989806 A ENSESTG00000000781 ENSESTT00000001899 Transcript intron_variant - - - - - - rs6501588 17:70989806 A ENSESTG00000000781 ENSESTT00000001911 Transcript intron_variant - - - - - - rs6501588 17:70989806 A ENSESTG00000000781 ENSESTT00000001901 Transcript intron_variant - - - - - - rs6501588 17:70989806 A CCDS54160.1 CCDS54160.1 Transcript intron_variant - - - - - - rs6501588 17:70989806 A CCDS11690.1 CCDS11690.1 Transcript intron_variant - - - - - - rs11077650 17:70994539 C 201266 NM_139177.3 Transcript intron_variant - - - - - - rs11077650 17:70994539 C 201266 NM_001159770.1 Transcript intron_variant - - - - - - rs11077650 17:70994539 C ENSESTG00000000781 ENSESTT00000001912 Transcript intron_variant - - - - - - rs11077650 17:70994539 C ENSESTG00000000781 ENSESTT00000001899 Transcript intron_variant - - - - - - rs11077650 17:70994539 C ENSESTG00000000781 ENSESTT00000001911 Transcript intron_variant - - - - - - rs11077650 17:70994539 C ENSESTG00000000781 ENSESTT00000001901 Transcript intron_variant - - - - - - rs11077650 17:70994539 C CCDS54160.1 CCDS54160.1 Transcript intron_variant - - - - - - rs11077650 17:70994539 C CCDS11690.1 CCDS11690.1 Transcript intron_variant - - - - - - rs4969013 17:71124104 A - - - intergenic_variant - - - - - - rs9302961 17:71345297 C 54549 NM_001144952.1 Transcript intron_variant - - - - - - rs9302961 17:71345297 C ENSESTG00000011968 ENSESTT00000030019 Transcript intron_variant - - - - - - rs9302961 17:71345297 C CCDS45769.1 CCDS45769.1 Transcript intron_variant - - - - - - rs9302961 17:71345297 C ENSESTG00000011967 ENSESTT00000030003 Transcript downstream_gene_variant - - - - - - DISTANCE=3396 rs1531493 17:72281559 G - ENSR00001352968 RegulatoryFeature regulatory_region_variant - - - - - - rs1531493 17:72281559 G CCDS58589.1 CCDS58589.1 Transcript intron_variant - - - - - - rs1531493 17:72281559 G ENSESTG00000011938 ENSESTT00000029926 Transcript intron_variant - - - - - - rs1531493 17:72281559 G 64446 NM_001172810.1 Transcript intron_variant - - - - - - rs1531493 17:72281559 G CCDS11697.1 CCDS11697.1 Transcript intron_variant - - - - - - rs1531493 17:72281559 G ENSESTG00000011938 ENSESTT00000029923 Transcript intron_variant - - - - - - rs1531493 17:72281559 G 64446 NM_023036.4 Transcript intron_variant - - - - - - rs4789053 17:72302304 G - ENSR00001538135 RegulatoryFeature regulatory_region_variant - - - - - - rs4789053 17:72302304 G CCDS58589.1 CCDS58589.1 Transcript intron_variant - - - - - - rs4789053 17:72302304 G 64446 NM_001172810.1 Transcript intron_variant - - - - - - rs4789053 17:72302304 G CCDS11697.1 CCDS11697.1 Transcript intron_variant - - - - - - rs4789053 17:72302304 G 64446 NM_023036.4 Transcript intron_variant - - - - - - rs2706504 17:72456753 G - - - intergenic_variant - - - - - - rs1183330 17:72639088 C - - - intergenic_variant - - - - - - rs7215850 17:72708563 C 326624 NM_175738.4 Transcript intron_variant - - - - - - rs7215850 17:72708563 C ENSESTG00000019373 ENSESTT00000048730 Transcript intron_variant - - - - - - rs7215850 17:72708563 C ENSESTG00000019373 ENSESTT00000048702 Transcript intron_variant - - - - - - rs7215850 17:72708563 C CCDS11703.1 CCDS11703.1 Transcript intron_variant - - - - - - rs7215850 17:72708563 C ENSESTG00000018256 ENSESTT00000046000 Transcript intron_variant - - - - - - rs7215850 17:72708563 C 146722 NM_139018.3 Transcript intron_variant - - - - - - rs7215850 17:72708563 C CCDS11704.1 CCDS11704.1 Transcript intron_variant - - - - - - rs56409377 17:72724213 G 326624 NM_175738.4 Transcript intron_variant - - - - - - rs56409377 17:72724213 G CCDS11703.1 CCDS11703.1 Transcript intron_variant - - - - - - rs56409377 17:72724213 G ENSESTG00000018256 ENSESTT00000046000 Transcript intron_variant - - - - - - rs7212248 17:72834071 G 2905 NM_000835.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4097 rs7212248 17:72834071 G 54868 NM_017728.3 Transcript 3_prime_UTR_variant 2898 - - - - - rs7212248 17:72834071 G CCDS32724.1 CCDS32724.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4503 rs7212248 17:72834071 G CCDS32723.1 CCDS32723.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1245 rs7212248 17:72834071 G ENSESTG00000018405 ENSESTT00000046309 Transcript downstream_gene_variant - - - - - - DISTANCE=1554 rs9914645 17:72941134 C 347741 NM_178233.1 Transcript intron_variant - - - - - - rs9914645 17:72941134 C CCDS11709.1 CCDS11709.1 Transcript intron_variant - - - - - - rs9914645 17:72941134 C ENSESTG00000018414 ENSESTT00000046345 Transcript downstream_gene_variant - - - - - - DISTANCE=1342 rs8077014 17:73333107 C ENSESTG00000018950 ENSESTT00000047801 Transcript intron_variant - - - - - - rs8077014 17:73333107 C CCDS11722.1 CCDS11722.1 Transcript intron_variant - - - - - - rs8077014 17:73333107 C 2885 NM_203506.2 Transcript intron_variant - - - - - - rs8077014 17:73333107 C CCDS11721.1 CCDS11721.1 Transcript intron_variant - - - - - - rs8077014 17:73333107 C ENSESTG00000018950 ENSESTT00000047825 Transcript intron_variant - - - - - - rs8077014 17:73333107 C 2885 NM_002086.4 Transcript intron_variant - - - - - - rs7215753 17:73489220 C ENSESTG00000018942 ENSESTT00000047653 Transcript intron_variant - - - - - - rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041574 Transcript downstream_gene_variant - - - - - - DISTANCE=1429 rs7215753 17:73489220 C ENSESTG00000016669 ENSESTT00000041844 Transcript upstream_gene_variant - - - - - - DISTANCE=3992 rs7215753 17:73489220 C ENSESTG00000016669 ENSESTT00000041855 Transcript upstream_gene_variant - - - - - - DISTANCE=4640 rs7215753 17:73489220 C CCDS32732.1 CCDS32732.1 Transcript intron_variant - - - - - - rs7215753 17:73489220 C ENSESTG00000016622 ENSESTT00000041772 Transcript upstream_gene_variant - - - - - - DISTANCE=2148 rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041638 Transcript downstream_gene_variant - - - - - - DISTANCE=1312 rs7215753 17:73489220 C 9772 NM_014738.4 Transcript intron_variant - - - - - - rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041655 Transcript downstream_gene_variant - - - - - - DISTANCE=1429 rs7215753 17:73489220 C ENSESTG00000016622 ENSESTT00000041764 Transcript intron_variant - - - - - - rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041651 Transcript downstream_gene_variant - - - - - - DISTANCE=1312 rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041594 Transcript downstream_gene_variant - - - - - - DISTANCE=1429 rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041588 Transcript downstream_gene_variant - - - - - - DISTANCE=1312 rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041607 Transcript downstream_gene_variant - - - - - - DISTANCE=1312 rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041641 Transcript downstream_gene_variant - - - - - - DISTANCE=1429 rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041563 Transcript downstream_gene_variant - - - - - - DISTANCE=1312 rs7215753 17:73489220 C ENSESTG00000016538 ENSESTT00000041614 Transcript downstream_gene_variant - - - - - - DISTANCE=1429 rs7503549 17:74402900 G ENSESTG00000010316 ENSESTT00000025815 Transcript intron_variant - - - - - - rs7503549 17:74402900 G 63893 NM_022066.3 Transcript intron_variant - - - - - - rs7503549 17:74402900 G ENSESTG00000010316 ENSESTT00000025818 Transcript upstream_gene_variant - - - - - - DISTANCE=4113 rs7503549 17:74402900 G CCDS32742.1 CCDS32742.1 Transcript intron_variant - - - - - - rs4238987 17:74428086 A ENSESTG00000010316 ENSESTT00000025815 Transcript intron_variant - - - - - - rs4238987 17:74428086 A 63893 NM_022066.3 Transcript intron_variant - - - - - - rs4238987 17:74428086 A CCDS32742.1 CCDS32742.1 Transcript intron_variant - - - - - - rs620100 17:75118631 C - ENSR00001353918 RegulatoryFeature regulatory_region_variant - - - - - - rs620100 17:75118631 C 6397 NM_001204408.1 Transcript intron_variant - - - - - - rs620100 17:75118631 C 6397 NM_001204410.1 Transcript intron_variant - - - - - - rs4789416 17:75164980 C - ENSR00001353938 RegulatoryFeature regulatory_region_variant - - - - - - rs4789416 17:75164980 C CCDS11752.1 CCDS11752.1 Transcript intron_variant - - - - - - rs4789416 17:75164980 C 6397 NM_001143998.1 Transcript intron_variant - - - - - - rs4789416 17:75164980 C 6397 NM_001039573.2 Transcript intron_variant - - - - - - rs4789416 17:75164980 C 6397 NM_001204410.1 Transcript intron_variant - - - - - - rs4789416 17:75164980 C CCDS42385.1 CCDS42385.1 Transcript intron_variant - - - - - - rs4789416 17:75164980 C 6397 NM_001204408.1 Transcript intron_variant - - - - - - rs4789416 17:75164980 C 6397 NM_003003.3 Transcript intron_variant - - - - - - rs4789416 17:75164980 C 6397 NM_001143999.1 Transcript intron_variant - - - - - - rs11077891 17:75165518 T CCDS11752.1 CCDS11752.1 Transcript intron_variant - - - - - - rs11077891 17:75165518 T 6397 NM_001143998.1 Transcript intron_variant - - - - - - rs11077891 17:75165518 T 6397 NM_001039573.2 Transcript intron_variant - - - - - - rs11077891 17:75165518 T 6397 NM_001204410.1 Transcript intron_variant - - - - - - rs11077891 17:75165518 T CCDS42385.1 CCDS42385.1 Transcript intron_variant - - - - - - rs11077891 17:75165518 T 6397 NM_001204408.1 Transcript intron_variant - - - - - - rs11077891 17:75165518 T 6397 NM_003003.3 Transcript intron_variant - - - - - - rs11077891 17:75165518 T 6397 NM_001143999.1 Transcript intron_variant - - - - - - rs312886 17:75362141 C - ENSR00001354011 RegulatoryFeature regulatory_region_variant - - - - - - rs312886 17:75362141 C 10801 NM_001113491.1 Transcript intron_variant - - - - - - rs312886 17:75362141 C 10801 NM_006640.4 Transcript intron_variant - - - - - - rs312886 17:75362141 C ENSESTG00000005599 ENSESTT00000014269 Transcript intron_variant - - - - - - rs312886 17:75362141 C 10801 NM_001113492.1 Transcript intron_variant - - - - - - rs312886 17:75362141 C ENSESTG00000005599 ENSESTT00000014265 Transcript intron_variant - - - - - - rs312886 17:75362141 C ENSESTG00000005599 ENSESTT00000014256 Transcript intron_variant - - - - - - rs312886 17:75362141 C CCDS45790.1 CCDS45790.1 Transcript intron_variant - - - - - - rs312886 17:75362141 C ENSESTG00000005599 ENSESTT00000014283 Transcript intron_variant - - - - - - rs312886 17:75362141 C ENSESTG00000005599 ENSESTT00000014238 Transcript intron_variant - - - - - - rs312886 17:75362141 C ENSESTG00000005599 ENSESTT00000014266 Transcript intron_variant - - - - - - rs312886 17:75362141 C ENSESTG00000005599 ENSESTT00000014279 Transcript intron_variant - - - - - - rs312886 17:75362141 C CCDS45791.1 CCDS45791.1 Transcript intron_variant - - - - - - rs312886 17:75362141 C ENSESTG00000005599 ENSESTT00000014276 Transcript intron_variant - - - - - - rs312886 17:75362141 C ENSESTG00000005599 ENSESTT00000014259 Transcript intron_variant - - - - - - rs405278 17:75377313 T 10801 NM_006640.4 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014269 Transcript intron_variant - - - - - - rs405278 17:75377313 T 10801 NM_001113494.1 Transcript intron_variant - - - - - - rs405278 17:75377313 T 10801 NM_001113492.1 Transcript intron_variant - - - - - - rs405278 17:75377313 T 10801 NM_001113493.1 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014256 Transcript intron_variant - - - - - - rs405278 17:75377313 T CCDS45790.1 CCDS45790.1 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014238 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014266 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014300 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014259 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014292 Transcript intron_variant - - - - - - rs405278 17:75377313 T 10801 NM_001113491.1 Transcript intron_variant - - - - - - rs405278 17:75377313 T CCDS45792.1 CCDS45792.1 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014309 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014265 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014279 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014283 Transcript intron_variant - - - - - - rs405278 17:75377313 T CCDS45791.1 CCDS45791.1 Transcript intron_variant - - - - - - rs405278 17:75377313 T ENSESTG00000005599 ENSESTT00000014276 Transcript intron_variant - - - - - - rs4789476 17:75618305 C - - - intergenic_variant - - - - - - rs7215328 17:75618996 G - - - intergenic_variant - - - - - - rs12450525 17:75692521 C - - - intergenic_variant - - - - - - rs4789515 17:75913177 C - ENSR00001354160 RegulatoryFeature regulatory_region_variant - - - - - - rs4789515 17:75913177 C - - - intergenic_variant - - - - - - rs10852787 17:75919441 G ENSESTG00000005724 ENSESTT00000014502 Transcript upstream_gene_variant - - - - - - DISTANCE=3090 rs6501204 17:76335257 C - ENSR00001354301 RegulatoryFeature regulatory_region_variant - - - - - - rs6501204 17:76335257 C ENSESTG00000003398 ENSESTT00000008494 Transcript intron_variant - - - - - - rs6501204 17:76335257 C ENSESTG00000003398 ENSESTT00000008497 Transcript upstream_gene_variant - - - - - - DISTANCE=3561 rs4969177 17:76378151 G - ENSR00001354324 RegulatoryFeature regulatory_region_variant - - - - - - rs4969177 17:76378151 G ENSESTG00000003409 ENSESTT00000008553 Transcript intron_variant - - - - - - rs4969177 17:76378151 G CCDS42391.1 CCDS42391.1 Transcript intron_variant - - - - - - rs4969177 17:76378151 G 9489 NM_024419.3 Transcript intron_variant - - - - - - rs4969177 17:76378151 G ENSESTG00000003409 ENSESTT00000008551 Transcript intron_variant - - - - - - rs4796818 17:76623924 G ENSESTG00000003682 ENSESTT00000009262 Transcript intron_variant - - - - - - rs4796818 17:76623924 G ENSESTG00000003682 ENSESTT00000009266 Transcript upstream_gene_variant - - - - - - DISTANCE=3524 rs12941191 17:77020542 G - ENSR00001538501 RegulatoryFeature regulatory_region_variant - - - - - - rs12941191 17:77020542 G ENSESTG00000003546 ENSESTT00000008852 Transcript intron_variant - - - - - - rs12941191 17:77020542 G ENSESTG00000003460 ENSESTT00000008659 Transcript intron_variant - - - - - - rs12941191 17:77020542 G 114897 NM_153372.1 Transcript intron_variant - - - - - - rs12941191 17:77020542 G ENSESTG00000003460 ENSESTT00000008674 Transcript stop_gained 290 9 3 Y/* taC/taG - rs12941191 17:77020542 G ENSESTG00000003460 ENSESTT00000008665 Transcript stop_gained 292 291 97 Y/* taC/taG - rs12941191 17:77020542 G 100507410 NR_040018.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs12941191 17:77020542 G 114897 NR_049769.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1203 rs12941191 17:77020542 G ENSESTG00000003546 ENSESTT00000008853 Transcript intron_variant - - - - - - rs12941191 17:77020542 G 100507410 NR_040019.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs12941191 17:77020542 G 114897 NM_030968.3 Transcript 5_prime_UTR_variant 385 - - - - - rs12941191 17:77020542 G ENSESTG00000003540 ENSESTT00000008843 Transcript intron_variant - - - - - - rs12941191 17:77020542 G ENSESTG00000003460 ENSESTT00000008660 Transcript stop_gained 385 9 3 Y/* taC/taG - rs12941191 17:77020542 G ENSESTG00000003460 ENSESTT00000008652 Transcript stop_gained 673 252 84 Y/* taC/taG - rs12941191 17:77020542 G 114897 NM_198594.2 Transcript 5_prime_UTR_variant 385 - - - - - rs7221703 17:77028479 G ENSESTG00000003546 ENSESTT00000008852 Transcript upstream_gene_variant - - - - - - DISTANCE=4742 rs7221703 17:77028479 G ENSESTG00000003460 ENSESTT00000008678 Transcript upstream_gene_variant - - - - - - DISTANCE=1902 rs7221703 17:77028479 G 114897 NM_153372.1 Transcript intron_variant - - - - - - rs7221703 17:77028479 G 100507410 NR_040018.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4742 rs7221703 17:77028479 G 114897 NR_049769.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7221703 17:77028479 G ENSESTG00000003546 ENSESTT00000008853 Transcript upstream_gene_variant - - - - - - DISTANCE=4777 rs7221703 17:77028479 G ENSESTG00000003540 ENSESTT00000008843 Transcript intron_variant - - - - - - rs7221703 17:77028479 G ENSESTG00000003460 ENSESTT00000008660 Transcript intron_variant - - - - - - rs7221703 17:77028479 G 114897 NM_198594.2 Transcript intron_variant - - - - - - rs7221703 17:77028479 G ENSESTG00000003460 ENSESTT00000008659 Transcript intron_variant - - - - - - rs7221703 17:77028479 G ENSESTG00000003460 ENSESTT00000008674 Transcript intron_variant - - - - - - rs7221703 17:77028479 G 100507410 NR_040019.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4742 rs7221703 17:77028479 G 114897 NM_030968.3 Transcript intron_variant - - - - - - rs7221703 17:77028479 G ENSESTG00000003482 ENSESTT00000008682 Transcript intron_variant - - - - - - rs7221703 17:77028479 G ENSESTG00000003460 ENSESTT00000008652 Transcript intron_variant - - - - - - rs7221703 17:77028479 G 114897 NM_198593.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1902 rs6501276 17:77048715 T CCDS11761.1 CCDS11761.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4545 rs6501276 17:77048715 T ENSESTG00000003460 ENSESTT00000008678 Transcript downstream_gene_variant - - - - - - DISTANCE=4766 rs6501276 17:77048715 T ENSESTG00000003460 ENSESTT00000008659 Transcript downstream_gene_variant - - - - - - DISTANCE=4766 rs6501276 17:77048715 T 114897 NM_153372.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2845 rs6501276 17:77048715 T CCDS11762.1 CCDS11762.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4545 rs6501276 17:77048715 T 114897 NR_049769.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2845 rs6501276 17:77048715 T 114897 NM_030968.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2845 rs6501276 17:77048715 T ENSESTG00000003540 ENSESTT00000008843 Transcript upstream_gene_variant - - - - - - DISTANCE=2845 rs6501276 17:77048715 T ENSESTG00000003460 ENSESTT00000008660 Transcript downstream_gene_variant - - - - - - DISTANCE=4536 rs6501276 17:77048715 T ENSESTG00000003460 ENSESTT00000008652 Transcript downstream_gene_variant - - - - - - DISTANCE=4536 rs6501276 17:77048715 T 114897 NM_198593.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2845 rs6501276 17:77048715 T 114897 NM_198594.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2845 rs4789943 17:77062775 C - - - intergenic_variant - - - - - - rs2612772 17:77188643 C - ENSR00001354612 RegulatoryFeature regulatory_region_variant - - - - - - rs2612772 17:77188643 C ENSESTG00000003517 ENSESTT00000008776 Transcript intron_variant - - - - - - rs2612772 17:77188643 C 146713 NM_001082575.1 Transcript intron_variant - - - - - - rs2612772 17:77188643 C ENSESTG00000003517 ENSESTT00000008765 Transcript intron_variant - - - - - - rs2612772 17:77188643 C ENSESTG00000003517 ENSESTT00000008767 Transcript intron_variant - - - - - - rs898527 17:77251419 G ENSESTG00000003517 ENSESTT00000008772 Transcript intron_variant - - - - - - rs898527 17:77251419 G 146713 NM_001082575.1 Transcript intron_variant - - - - - - rs898527 17:77251419 G ENSESTG00000003517 ENSESTT00000008765 Transcript intron_variant - - - - - - rs898527 17:77251419 G ENSESTG00000003517 ENSESTT00000008767 Transcript intron_variant - - - - - - rs9302894 17:77371612 G ENSESTG00000003517 ENSESTT00000008772 Transcript intron_variant - - - - - - rs9302894 17:77371612 G ENSESTG00000003517 ENSESTT00000008765 Transcript intron_variant - - - - - - rs9302894 17:77371612 G ENSESTG00000003517 ENSESTT00000008767 Transcript intron_variant - - - - - - rs6565674 17:78298938 G ENSESTG00000005406 ENSESTT00000013780 Transcript missense_variant 1618 1603 535 N/D Aat/Gat - rs6565674 17:78298938 G CCDS58606.1 CCDS58606.1 Transcript missense_variant 3133 3133 1045 N/D Aat/Gat - PolyPhen=benign;SIFT=tolerated rs6565674 17:78298938 G 57674 NM_020954.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3675 rs6565674 17:78298938 G ENSESTG00000005406 ENSESTT00000013772 Transcript missense_variant 1618 1603 535 N/D Aat/Gat - rs6565674 17:78298938 G 57674 NM_001256071.1 Transcript missense_variant 3283 3133 1045 N/D Aat/Gat - PolyPhen=benign;SIFT=tolerated rs8074141 17:78410522 C CCDS54173.1 CCDS54173.1 Transcript downstream_gene_variant - - - - - - DISTANCE=579 rs8074141 17:78410522 C ENSESTG00000005679 ENSESTT00000014438 Transcript downstream_gene_variant - - - - - - DISTANCE=110 rs8074141 17:78410522 C ENSESTG00000005679 ENSESTT00000014470 Transcript downstream_gene_variant - - - - - - DISTANCE=110 rs8074141 17:78410522 C 284131 NM_001164637.1 Transcript 3_prime_UTR_variant 1321 - - - - - rs8074141 17:78410522 C ENSESTG00000005679 ENSESTT00000014473 Transcript downstream_gene_variant - - - - - - DISTANCE=110 rs8074141 17:78410522 C 284131 NM_173627.3 Transcript 3_prime_UTR_variant 1456 - - - - - rs8074141 17:78410522 C CCDS54172.1 CCDS54172.1 Transcript downstream_gene_variant - - - - - - DISTANCE=579 rs4890024 17:78425281 G - - - intergenic_variant - - - - - - rs6565503 17:78933424 G - ENSR00001538633 RegulatoryFeature regulatory_region_variant - - - - - - rs6565503 17:78933424 G ENSESTG00000005790 ENSESTT00000014702 Transcript intron_variant - - - - - - rs6565503 17:78933424 G ENSESTG00000005790 ENSESTT00000014682 Transcript intron_variant - - - - - - rs6565503 17:78933424 G CCDS54175.1 CCDS54175.1 Transcript intron_variant - - - - - - rs6565503 17:78933424 G CCDS11773.1 CCDS11773.1 Transcript intron_variant - - - - - - rs6565503 17:78933424 G 57521 NM_020761.2 Transcript intron_variant - - - - - - rs6565503 17:78933424 G 57521 NM_001163034.1 Transcript intron_variant - - - - - - rs4969327 17:78962970 C - ENSR00001355079 RegulatoryFeature regulatory_region_variant - - - - - - rs4969327 17:78962970 C ENSESTG00000005829 ENSESTT00000014828 Transcript upstream_gene_variant - - - - - - DISTANCE=2674 rs4969327 17:78962970 C CCDS11774.1 CCDS11774.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2749 rs4969327 17:78962970 C 79643 NM_024591.4 Transcript upstream_gene_variant - - - - - - DISTANCE=2671 rs4969327 17:78962970 C ENSESTG00000005829 ENSESTT00000014813 Transcript upstream_gene_variant - - - - - - DISTANCE=2428 rs9901252 17:79018596 C - ENSR00001355106 RegulatoryFeature regulatory_region_variant - - - - - - rs9901252 17:79018596 C CCDS11777.1 CCDS11777.1 Transcript intron_variant - - - - - - rs9901252 17:79018596 C 10458 NM_001144888.1 Transcript intron_variant - - - - - - rs9901252 17:79018596 C ENSESTG00000005920 ENSESTT00000015057 Transcript intron_variant - - - - - - rs9901252 17:79018596 C ENSESTG00000005920 ENSESTT00000015058 Transcript intron_variant - - - - - - rs9901252 17:79018596 C ENSESTG00000005920 ENSESTT00000015052 Transcript intron_variant - - - - - - rs9901252 17:79018596 C ENSESTG00000005920 ENSESTT00000015064 Transcript intron_variant - - - - - - rs9901252 17:79018596 C CCDS11775.1 CCDS11775.1 Transcript intron_variant - - - - - - rs9901252 17:79018596 C CCDS11776.1 CCDS11776.1 Transcript intron_variant - - - - - - rs9901252 17:79018596 C ENSESTG00000005920 ENSESTT00000015061 Transcript intron_variant - - - - - - rs9901252 17:79018596 C 10458 NM_017451.2 Transcript intron_variant - - - - - - rs9901252 17:79018596 C ENSESTG00000005920 ENSESTT00000015066 Transcript intron_variant - - - - - - rs9901252 17:79018596 C CCDS45806.1 CCDS45806.1 Transcript intron_variant - - - - - - rs9901252 17:79018596 C 10458 NM_006340.2 Transcript intron_variant - - - - - - rs9901252 17:79018596 C ENSESTG00000005920 ENSESTT00000015069 Transcript intron_variant - - - - - - rs9901252 17:79018596 C 10458 NM_017450.2 Transcript intron_variant - - - - - - rs11150787 17:79429318 C - ENSR00001355302 RegulatoryFeature regulatory_region_variant - - - - - - rs11150787 17:79429318 C ENSESTG00000027355 ENSESTT00000068908 Transcript downstream_gene_variant - - - - - - DISTANCE=1584 rs11150787 17:79429318 C ENSESTG00000027332 ENSESTT00000068869 Transcript downstream_gene_variant - - - - - - DISTANCE=3207 rs11150787 17:79429318 C ENSESTG00000027355 ENSESTT00000068889 Transcript downstream_gene_variant - - - - - - DISTANCE=1275 rs11150787 17:79429318 C ENSESTG00000027370 ENSESTT00000068972 Transcript upstream_gene_variant - - - - - - DISTANCE=267 rs11150787 17:79429318 C ENSESTG00000027370 ENSESTT00000068949 Transcript intron_variant - - - - - - rs11150787 17:79429318 C 57597 NM_001080519.2 Transcript intron_variant - - - - - - rs148465663 17:79474611 A - ENSR00001355331 RegulatoryFeature regulatory_region_variant - - - - - - rs148465663 17:79474611 A ENSESTG00000030749 ENSESTT00000077465 Transcript downstream_gene_variant - - - - - - DISTANCE=3813 rs148465663 17:79474611 A ENSESTG00000030749 ENSESTT00000077542 Transcript downstream_gene_variant - - - - - - DISTANCE=3204 rs148465663 17:79474611 A ENSESTG00000030749 ENSESTT00000077488 Transcript downstream_gene_variant - - - - - - DISTANCE=2869 rs148465663 17:79474611 A ENSESTG00000030749 ENSESTT00000077444 Transcript downstream_gene_variant - - - - - - DISTANCE=3889 rs148465663 17:79474611 A 71 NR_037688.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2386 rs148465663 17:79474611 A CCDS11782.1 CCDS11782.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3105 rs148465663 17:79474611 A 71 NM_001199954.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2386 rs148465663 17:79474611 A ENSESTG00000030749 ENSESTT00000077605 Transcript downstream_gene_variant - - - - - - DISTANCE=2725 rs148465663 17:79474611 A ENSESTG00000030749 ENSESTT00000077610 Transcript downstream_gene_variant - - - - - - DISTANCE=2894 rs148465663 17:79474611 A 71 NM_001614.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2386 rs148465663 17:79474611 A ENSESTG00000030749 ENSESTT00000077590 Transcript downstream_gene_variant - - - - - - DISTANCE=3814 rs141784459 17:79474679 C - ENSR00001355331 RegulatoryFeature regulatory_region_variant - - - - - - rs141784459 17:79474679 C ENSESTG00000030749 ENSESTT00000077465 Transcript downstream_gene_variant - - - - - - DISTANCE=3745 rs141784459 17:79474679 C ENSESTG00000030749 ENSESTT00000077542 Transcript downstream_gene_variant - - - - - - DISTANCE=3136 rs141784459 17:79474679 C ENSESTG00000030749 ENSESTT00000077488 Transcript downstream_gene_variant - - - - - - DISTANCE=2801 rs141784459 17:79474679 C ENSESTG00000030749 ENSESTT00000077444 Transcript downstream_gene_variant - - - - - - DISTANCE=3821 rs141784459 17:79474679 C 71 NR_037688.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2318 rs141784459 17:79474679 C CCDS11782.1 CCDS11782.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3037 rs141784459 17:79474679 C 71 NM_001199954.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2318 rs141784459 17:79474679 C ENSESTG00000030749 ENSESTT00000077605 Transcript downstream_gene_variant - - - - - - DISTANCE=2657 rs141784459 17:79474679 C ENSESTG00000030749 ENSESTT00000077610 Transcript downstream_gene_variant - - - - - - DISTANCE=2826 rs141784459 17:79474679 C 71 NM_001614.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2318 rs141784459 17:79474679 C ENSESTG00000030749 ENSESTT00000077590 Transcript downstream_gene_variant - - - - - - DISTANCE=3746 rs1879568 17:79872129 G CCDS11792.1 CCDS11792.1 Transcript intron_variant - - - - - - rs1879568 17:79872129 G CCDS11791.1 CCDS11791.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2898 rs1879568 17:79872129 G ENSESTG00000030028 ENSESTT00000075673 Transcript downstream_gene_variant - - - - - - DISTANCE=1212 rs1879568 17:79872129 G 5833 NM_002861.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2789 rs1879568 17:79872129 G ENSESTG00000030105 ENSESTT00000075874 Transcript upstream_gene_variant - - - - - - DISTANCE=2847 rs1879568 17:79872129 G ENSESTG00000030105 ENSESTT00000075908 Transcript upstream_gene_variant - - - - - - DISTANCE=3093 rs1879568 17:79872129 G 5833 NR_033685.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3052 rs1879568 17:79872129 G ENSESTG00000030028 ENSESTT00000075685 Transcript downstream_gene_variant - - - - - - DISTANCE=1186 rs1879568 17:79872129 G ENSESTG00000030028 ENSESTT00000075656 Transcript downstream_gene_variant - - - - - - DISTANCE=1132 rs1879568 17:79872129 G CCDS54178.1 CCDS54178.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2898 rs1879568 17:79872129 G ENSESTG00000030105 ENSESTT00000075887 Transcript upstream_gene_variant - - - - - - DISTANCE=3078 rs1879568 17:79872129 G ENSESTG00000030028 ENSESTT00000075611 Transcript intron_variant - - - - - - rs1879568 17:79872129 G 5833 NM_001256434.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2789 rs1879568 17:79872129 G ENSESTG00000030028 ENSESTT00000075719 Transcript intron_variant - - - - - - rs1879568 17:79872129 G 5833 NM_001256433.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2789 rs1879568 17:79872129 G 4097 NM_032711.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4016 rs1879568 17:79872129 G ENSESTG00000028072 ENSESTT00000070601 Transcript missense_variant 165 118 40 R/G Agg/Ggg - rs1879568 17:79872129 G ENSESTG00000028080 ENSESTT00000070616 Transcript upstream_gene_variant - - - - - - DISTANCE=2358 rs1879568 17:79872129 G 4097 NM_002359.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4016 rs1879568 17:79872129 G 51547 NM_016538.2 Transcript intron_variant - - - - - - rs1879568 17:79872129 G 5833 NM_001256435.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2789 rs1879568 17:79872129 G 5833 NR_033683.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3052 rs1879568 17:79872129 G 5833 NM_001184917.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2789 rs6502046 17:79973528 C - ENSR00001355514 RegulatoryFeature regulatory_region_variant - - - - - - rs6502046 17:79973528 C 79058 NM_024083.3 Transcript intron_variant - - - - - - rs6502046 17:79973528 C ENSESTG00000028141 ENSESTT00000071069 Transcript intron_variant - - - - - - rs6502046 17:79973528 C 79058 NR_045351.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6502046 17:79973528 C ENSESTG00000028141 ENSESTT00000071116 Transcript intron_variant - - - - - - rs6502046 17:79973528 C CCDS58611.1 CCDS58611.1 Transcript intron_variant - - - - - - rs6502046 17:79973528 C CCDS11796.1 CCDS11796.1 Transcript intron_variant - - - - - - rs6502046 17:79973528 C ENSESTG00000028141 ENSESTT00000070980 Transcript intron_variant - - - - - - rs6502046 17:79973528 C 79058 NM_001251888.1 Transcript intron_variant - - - - - - rs6502046 17:79973528 C 201254 NM_144998.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3051 rs6502046 17:79973528 C ENSESTG00000029820 ENSESTT00000075072 Transcript downstream_gene_variant - - - - - - DISTANCE=3323 rs6502046 17:79973528 C ENSESTG00000028141 ENSESTT00000071010 Transcript intron_variant - - - - - - rs6502046 17:79973528 C ENSESTG00000028141 ENSESTT00000071046 Transcript intron_variant - - - - - - rs6502046 17:79973528 C ENSESTG00000028141 ENSESTT00000071143 Transcript upstream_gene_variant - - - - - - DISTANCE=542 rs6502046 17:79973528 C ENSESTG00000029820 ENSESTT00000075054 Transcript downstream_gene_variant - - - - - - DISTANCE=3398 rs6502046 17:79973528 C CCDS32772.1 CCDS32772.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3553 rs6502046 17:79973528 C ENSESTG00000029820 ENSESTT00000075043 Transcript downstream_gene_variant - - - - - - DISTANCE=3338 rs56974641 17:80105647 G 284001 NM_198082.2 Transcript intron_variant - - - - - - rs56974641 17:80105647 G ENSESTG00000028874 ENSESTT00000072697 Transcript intron_variant - - - - - - rs56974641 17:80105647 G ENSESTG00000028874 ENSESTT00000072738 Transcript intron_variant - - - - - - rs2379119 17:80624465 C ENSESTG00000011379 ENSESTT00000028577 Transcript intron_variant - - - - - - rs2379119 17:80624465 C 100616196 NR_039751.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1644 rs2379119 17:80624465 C ENSESTG00000011379 ENSESTT00000028580 Transcript intron_variant - - - - - - rs2379119 17:80624465 C CCDS11816.1 CCDS11816.1 Transcript intron_variant - - - - - - rs2379119 17:80624465 C 10966 NM_006822.2 Transcript intron_variant - - - - - - rs2379119 17:80624465 C ENSESTG00000011379 ENSESTT00000028583 Transcript intron_variant - - - - - - rs12451351 17:80628236 T ENSESTG00000011379 ENSESTT00000028577 Transcript intron_variant - - - - - - rs12451351 17:80628236 T 100616196 NR_039751.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2053 rs12451351 17:80628236 T ENSESTG00000011379 ENSESTT00000028580 Transcript intron_variant - - - - - - rs12451351 17:80628236 T CCDS11816.1 CCDS11816.1 Transcript intron_variant - - - - - - rs12451351 17:80628236 T 10966 NM_006822.2 Transcript intron_variant - - - - - - rs12451351 17:80628236 T ENSESTG00000011379 ENSESTT00000028583 Transcript intron_variant - - - - - - rs2451210 17:80698395 G 64122 NM_022158.3 Transcript intron_variant - - - - - - rs2451210 17:80698395 G ENSESTG00000011231 ENSESTT00000028136 Transcript intron_variant - - - - - - rs2451210 17:80698395 G CCDS11818.1 CCDS11818.1 Transcript intron_variant - - - - - - rs2451210 17:80698395 G ENSESTG00000011231 ENSESTT00000028137 Transcript intron_variant - - - - - - rs2890157 17:80793034 C 79755 NM_024702.2 Transcript intron_variant - - - - - - rs2890157 17:80793034 C ENSESTG00000011240 ENSESTT00000028142 Transcript downstream_gene_variant - - - - - - DISTANCE=1561 rs2890157 17:80793034 C CCDS45818.1 CCDS45818.1 Transcript intron_variant - - - - - - rs2890157 17:80793034 C CCDS11819.1 CCDS11819.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2704 rs2890157 17:80793034 C 6904 NM_005993.4 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028357 Transcript intron_variant - - - - - - rs9894419 17:80828575 G CCDS45818.1 CCDS45818.1 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028333 Transcript intron_variant - - - - - - rs9894419 17:80828575 G 6904 NM_005993.4 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028404 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028397 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028393 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028389 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028364 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028324 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028327 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028380 Transcript intron_variant - - - - - - rs9894419 17:80828575 G ENSESTG00000011252 ENSESTT00000028351 Transcript intron_variant - - - - - - rs7213533 17:80844915 A - ENSR00001355856 RegulatoryFeature regulatory_region_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028357 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028407 Transcript intron_variant - - - - - - rs7213533 17:80844915 A CCDS45818.1 CCDS45818.1 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028333 Transcript intron_variant - - - - - - rs7213533 17:80844915 A 6904 NM_005993.4 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028404 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028397 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028393 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028389 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028364 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028324 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028327 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028408 Transcript upstream_gene_variant - - - - - - DISTANCE=1678 rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028380 Transcript intron_variant - - - - - - rs7213533 17:80844915 A ENSESTG00000011252 ENSESTT00000028351 Transcript intron_variant - - - - - - rs7406436 17:81036261 C - ENSR00001355911 RegulatoryFeature regulatory_region_variant - - - - - - rs7406436 17:81036261 C CCDS32779.1 CCDS32779.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1431 rs7406436 17:81036261 C ENSESTG00000011331 ENSESTT00000028452 Transcript upstream_gene_variant - - - - - - DISTANCE=1306 rs7406436 17:81036261 C 284207 NM_001004431.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1306 rs7406436 17:81036261 C ENSESTG00000011331 ENSESTT00000028477 Transcript upstream_gene_variant - - - - - - DISTANCE=1814 rs4986108 17:81049620 G - ENSR00001355925 RegulatoryFeature regulatory_region_variant - - - - - - rs4986108 17:81049620 G CCDS32779.1 CCDS32779.1 Transcript intron_variant - - - - - - rs4986108 17:81049620 G 284207 NM_001004431.1 Transcript intron_variant - - - - - - rs4986108 17:81049620 G ENSESTG00000011331 ENSESTT00000028477 Transcript intron_variant - - - - - - rs4986108 17:81049620 G ENSESTG00000011331 ENSESTT00000028484 Transcript upstream_gene_variant - - - - - - DISTANCE=576 rs657942 18:344536 C ENSESTG00000002492 ENSESTT00000006163 Transcript downstream_gene_variant - - - - - - DISTANCE=2376 rs657942 18:344536 C ENSESTG00000002313 ENSESTT00000005740 Transcript intron_variant - - - - - - rs657942 18:344536 C ENSESTG00000002496 ENSESTT00000006181 Transcript intron_variant - - - - - - rs657942 18:344536 C CCDS32782.1 CCDS32782.1 Transcript intron_variant - - - - - - rs657942 18:344536 C 81035 NM_130386.2 Transcript intron_variant - - - - - - rs3929953 18:368220 A CCDS32782.1 CCDS32782.1 Transcript intron_variant - - - - - - rs3929953 18:368220 A 81035 NM_130386.2 Transcript intron_variant - - - - - - rs2925479 18:640763 T 27098 NM_014410.4 Transcript intron_variant - - - - - - rs2925479 18:640763 T CCDS42405.1 CCDS42405.1 Transcript intron_variant - - - - - - rs2925479 18:640763 T ENSESTG00000002336 ENSESTT00000005804 Transcript intron_variant - - - - - - rs2925479 18:640763 T ENSESTG00000002336 ENSESTT00000005809 Transcript upstream_gene_variant - - - - - - DISTANCE=709 rs2925479 18:640763 T ENSESTG00000002336 ENSESTT00000005800 Transcript intron_variant - - - - - - rs2925479 18:640763 T 27098 NM_199167.1 Transcript intron_variant - - - - - - rs2925479 18:640763 T ENSESTG00000002485 ENSESTT00000006145 Transcript downstream_gene_variant - - - - - - DISTANCE=561 rs4392142 18:849865 C - - - intergenic_variant - - - - - - rs789044 18:1020301 T - - - intergenic_variant - - - - - - rs304406 18:1103506 G - - - intergenic_variant - - - - - - rs4505415 18:1324536 A 56651 NR_023926.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4505415 18:1324536 A 56651 NR_023925.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4505415 18:1324536 A 56651 NR_023927.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4797937 18:1638892 C ENSESTG00000000808 ENSESTT00000001962 Transcript intron_variant - - - - - - rs2846863 18:2195391 C - - - intergenic_variant - - - - - - rs6505998 18:2239489 A - - - intergenic_variant - - - - - - rs1519577 18:2324401 C - ENSR00000276139 RegulatoryFeature regulatory_region_variant - - - - - - rs1519577 18:2324401 C - - - intergenic_variant - - - - - - rs8092770 18:2348318 C - - - intergenic_variant - - - - - - rs3848492 18:2366452 G - - - intergenic_variant - - - - - - rs3914858 18:2368006 A - - - intergenic_variant - - - - - - rs7234152 18:2371953 T - - - intergenic_variant - - - - - - rs7227462 18:2414166 A - - - intergenic_variant - - - - - - rs1539792 18:2982817 A - ENSR00000276186 RegulatoryFeature regulatory_region_variant - - - - - - rs1539792 18:2982817 A ENSESTG00000013506 ENSESTT00000033815 Transcript intron_variant - - - - - - rs1539792 18:2982817 A ENSESTG00000015264 ENSESTT00000038276 Transcript 5_prime_UTR_variant 80 - - - - - rs1539792 18:2982817 A 9663 NM_014646.2 Transcript intron_variant - - - - - - rs7245051 18:3322689 T ENSESTG00000013576 ENSESTT00000033951 Transcript intron_variant - - - - - - rs2852262 18:3349773 T - - - intergenic_variant - - - - - - rs6506118 18:3382754 A - - - intergenic_variant - - - - - - rs6506126 18:3428889 A 7050 NM_174886.1 Transcript intron_variant - - - - - - rs6506126 18:3428889 A ENSESTG00000013588 ENSESTT00000033989 Transcript intron_variant - - - - - - rs8084143 18:3771656 C - ENSR00000521515 RegulatoryFeature regulatory_region_variant - - - - - - rs8084143 18:3771656 C ENSESTG00000013666 ENSESTT00000034177 Transcript intron_variant - - - - - - rs8084143 18:3771656 C CCDS56052.1 CCDS56052.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C 9229 NM_001242763.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C 9229 NM_001242764.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C CCDS56051.1 CCDS56051.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C 9229 NM_001242765.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C CCDS56053.1 CCDS56053.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C CCDS42406.1 CCDS42406.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C ENSESTG00000013666 ENSESTT00000034185 Transcript intron_variant - - - - - - rs8084143 18:3771656 C CCDS56050.1 CCDS56050.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C 9229 NM_001003809.2 Transcript intron_variant - - - - - - rs8084143 18:3771656 C 9229 NM_004746.3 Transcript intron_variant - - - - - - rs8084143 18:3771656 C 9229 NM_001242762.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C CCDS56049.1 CCDS56049.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C CCDS11836.1 CCDS11836.1 Transcript intron_variant - - - - - - rs8084143 18:3771656 C 9229 NM_001242766.1 Transcript intron_variant - - - - - - rs1442387 18:3932491 G ENSESTG00000013655 ENSESTT00000034159 Transcript intron_variant - - - - - - rs1442387 18:3932491 G 9229 NM_004746.3 Transcript intron_variant - - - - - - rs1442387 18:3932491 G 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs4798151 18:3941421 G ENSESTG00000013655 ENSESTT00000034159 Transcript intron_variant - - - - - - rs4798151 18:3941421 G 9229 NM_004746.3 Transcript intron_variant - - - - - - rs4798151 18:3941421 G 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs1442380 18:3971628 C ENSESTG00000013655 ENSESTT00000034159 Transcript intron_variant - - - - - - rs1442380 18:3971628 C 9229 NM_004746.3 Transcript intron_variant - - - - - - rs1442380 18:3971628 C 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs8092466 18:4039419 A ENSESTG00000017248 ENSESTT00000043343 Transcript intron_variant - - - - - - rs8092466 18:4039419 A ENSESTG00000013655 ENSESTT00000034159 Transcript intron_variant - - - - - - rs8092466 18:4039419 A 9229 NM_004746.3 Transcript intron_variant - - - - - - rs8092466 18:4039419 A ENSESTG00000017248 ENSESTT00000043336 Transcript intron_variant - - - - - - rs8092466 18:4039419 A ENSESTG00000017248 ENSESTT00000043325 Transcript intron_variant - - - - - - rs8092466 18:4039419 A 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs981278 18:4046337 A ENSESTG00000017248 ENSESTT00000043343 Transcript intron_variant - - - - - - rs981278 18:4046337 A ENSESTG00000013655 ENSESTT00000034159 Transcript intron_variant - - - - - - rs981278 18:4046337 A 9229 NM_004746.3 Transcript intron_variant - - - - - - rs981278 18:4046337 A ENSESTG00000017248 ENSESTT00000043336 Transcript intron_variant - - - - - - rs981278 18:4046337 A ENSESTG00000017248 ENSESTT00000043325 Transcript intron_variant - - - - - - rs981278 18:4046337 A 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs1442371 18:4051081 C ENSESTG00000017248 ENSESTT00000043343 Transcript intron_variant - - - - - - rs1442371 18:4051081 C ENSESTG00000013655 ENSESTT00000034159 Transcript intron_variant - - - - - - rs1442371 18:4051081 C 9229 NM_004746.3 Transcript intron_variant - - - - - - rs1442371 18:4051081 C ENSESTG00000017248 ENSESTT00000043336 Transcript intron_variant - - - - - - rs1442371 18:4051081 C ENSESTG00000017248 ENSESTT00000043325 Transcript intron_variant - - - - - - rs1442371 18:4051081 C 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs1442375 18:4055436 C ENSESTG00000017248 ENSESTT00000043343 Transcript intron_variant - - - - - - rs1442375 18:4055436 C ENSESTG00000013655 ENSESTT00000034159 Transcript intron_variant - - - - - - rs1442375 18:4055436 C 9229 NM_004746.3 Transcript intron_variant - - - - - - rs1442375 18:4055436 C ENSESTG00000017248 ENSESTT00000043336 Transcript intron_variant - - - - - - rs1442375 18:4055436 C ENSESTG00000017248 ENSESTT00000043325 Transcript intron_variant - - - - - - rs1442375 18:4055436 C 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs7236926 18:4169312 C 9229 NM_004746.3 Transcript intron_variant - - - - - - rs7236926 18:4169312 C ENSESTG00000017248 ENSESTT00000043336 Transcript intron_variant - - - - - - rs7236926 18:4169312 C ENSESTG00000017248 ENSESTT00000043325 Transcript intron_variant - - - - - - rs7236926 18:4169312 C 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs647182 18:4305092 C 9229 NM_004746.3 Transcript intron_variant - - - - - - rs647182 18:4305092 C 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs611533 18:4329752 A 9229 NM_004746.3 Transcript intron_variant - - - - - - rs611533 18:4329752 A 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs689409 18:4331845 A 9229 NM_004746.3 Transcript intron_variant - - - - - - rs689409 18:4331845 A 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs565402 18:4332349 G 9229 NM_004746.3 Transcript intron_variant - - - - - - rs565402 18:4332349 G 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs579525 18:4338145 C 9229 NM_004746.3 Transcript intron_variant - - - - - - rs579525 18:4338145 C 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs672639 18:4340892 G 9229 NM_004746.3 Transcript intron_variant - - - - - - rs672639 18:4340892 G 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs550394 18:4360674 G 9229 NM_004746.3 Transcript intron_variant - - - - - - rs550394 18:4360674 G 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs694144 18:4376516 G 9229 NM_004746.3 Transcript intron_variant - - - - - - rs694144 18:4376516 G 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs586451 18:4379619 T 9229 NM_004746.3 Transcript intron_variant - - - - - - rs586451 18:4379619 T 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs655507 18:4390121 A 9229 NM_004746.3 Transcript intron_variant - - - - - - rs655507 18:4390121 A 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs2199542 18:4397871 G 9229 NM_004746.3 Transcript intron_variant - - - - - - rs2199542 18:4397871 G 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs2320212 18:4400001 T - ENSR00000521589 RegulatoryFeature regulatory_region_variant - - - - - - rs2320212 18:4400001 T 9229 NM_004746.3 Transcript intron_variant - - - - - - rs2320212 18:4400001 T 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs11081104 18:4406228 G - ENSR00000521590 RegulatoryFeature regulatory_region_variant - - - - - - rs11081104 18:4406228 G 9229 NM_004746.3 Transcript intron_variant - - - - - - rs11081104 18:4406228 G 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs281016 18:4417533 A 9229 NM_004746.3 Transcript intron_variant - - - - - - rs281016 18:4417533 A 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs281006 18:4422329 A 9229 NM_004746.3 Transcript intron_variant - - - - - - rs281006 18:4422329 A 9229 NM_001242761.1 Transcript intron_variant - - - - - - rs9967093 18:4646608 C - - - intergenic_variant - - - - - - rs8082871 18:4674511 T - - - intergenic_variant - - - - - - rs12960825 18:4802742 A - - - intergenic_variant - - - - - - rs4798252 18:4806790 G - - - intergenic_variant - - - - - - rs4798253 18:4812055 T - - - intergenic_variant - - - - - - rs4797186 18:4818945 G - - - intergenic_variant - - - - - - rs6506258 18:4878895 T - - - intergenic_variant - - - - - - rs4503894 18:4891093 A - - - intergenic_variant - - - - - - rs4798259 18:4900601 T - - - intergenic_variant - - - - - - rs12960538 18:4937458 T - - - intergenic_variant - - - - - - rs7504628 18:4957572 A - - - intergenic_variant - - - - - - rs6506269 18:4961235 C - - - intergenic_variant - - - - - - rs6506273 18:4968753 C - - - intergenic_variant - - - - - - rs502682 18:5926795 G - - - intergenic_variant - - - - - - rs667157 18:5961192 C ENSESTG00000012577 ENSESTT00000031598 Transcript intron_variant - - - - - - rs667157 18:5961192 C 91133 NM_173464.3 Transcript intron_variant - - - - - - rs667157 18:5961192 C CCDS11839.2 CCDS11839.2 Transcript intron_variant - - - - - - rs667157 18:5961192 C ENSESTG00000012577 ENSESTT00000031605 Transcript intron_variant - - - - - - rs628170 18:5978233 T ENSESTG00000012577 ENSESTT00000031598 Transcript intron_variant - - - - - - rs628170 18:5978233 T 91133 NM_173464.3 Transcript intron_variant - - - - - - rs628170 18:5978233 T CCDS11839.2 CCDS11839.2 Transcript intron_variant - - - - - - rs385531 18:6280742 A ENSESTG00000012577 ENSESTT00000031603 Transcript intron_variant - - - - - - rs385531 18:6280742 A ENSESTG00000012577 ENSESTT00000031598 Transcript intron_variant - - - - - - rs385531 18:6280742 A ENSESTG00000012577 ENSESTT00000031601 Transcript intron_variant - - - - - - rs385531 18:6280742 A 91133 NM_173464.3 Transcript intron_variant - - - - - - rs385531 18:6280742 A CCDS11839.2 CCDS11839.2 Transcript intron_variant - - - - - - rs341189 18:6334353 C ENSESTG00000012577 ENSESTT00000031603 Transcript intron_variant - - - - - - rs341189 18:6334353 C ENSESTG00000012577 ENSESTT00000031598 Transcript intron_variant - - - - - - rs341189 18:6334353 C ENSESTG00000012577 ENSESTT00000031601 Transcript intron_variant - - - - - - rs341189 18:6334353 C 91133 NM_173464.3 Transcript intron_variant - - - - - - rs341175 18:6354208 C ENSESTG00000012577 ENSESTT00000031603 Transcript intron_variant - - - - - - rs341175 18:6354208 C ENSESTG00000012577 ENSESTT00000031598 Transcript intron_variant - - - - - - rs341175 18:6354208 C ENSESTG00000012577 ENSESTT00000031601 Transcript intron_variant - - - - - - rs341175 18:6354208 C 91133 NM_173464.3 Transcript intron_variant - - - - - - rs519120 18:6941138 C CCDS32787.1 CCDS32787.1 Transcript downstream_gene_variant - - - - - - DISTANCE=940 rs519120 18:6941138 C ENSESTG00000018997 ENSESTT00000047897 Transcript downstream_gene_variant - - - - - - DISTANCE=750 rs519120 18:6941138 C 284217 NM_005559.3 Transcript downstream_gene_variant - - - - - - DISTANCE=605 rs519120 18:6941138 C ENSESTG00000018997 ENSESTT00000047769 Transcript downstream_gene_variant - - - - - - DISTANCE=747 rs6506466 18:7058741 C CCDS32787.1 CCDS32787.1 Transcript intron_variant - - - - - - rs6506466 18:7058741 C 284217 NM_005559.3 Transcript intron_variant - - - - - - rs6506466 18:7058741 C ENSESTG00000019057 ENSESTT00000047927 Transcript intron_variant - - - - - - rs1624572 18:7452040 G - - - intergenic_variant - - - - - - rs546947 18:7532210 T - - - intergenic_variant - - - - - - rs9957938 18:7878261 G - ENSR00000521891 RegulatoryFeature regulatory_region_variant - - - - - - rs9957938 18:7878261 G ENSESTG00000018948 ENSESTT00000047685 Transcript intron_variant - - - - - - rs9957938 18:7878261 G 5797 NM_001105244.1 Transcript intron_variant - - - - - - rs9957938 18:7878261 G CCDS11840.1 CCDS11840.1 Transcript intron_variant - - - - - - rs9957938 18:7878261 G 5797 NM_002845.3 Transcript intron_variant - - - - - - rs9957938 18:7878261 G CCDS58613.1 CCDS58613.1 Transcript intron_variant - - - - - - rs1860962 18:8199477 A ENSESTG00000005119 ENSESTT00000013102 Transcript intron_variant - - - - - - rs1860962 18:8199477 A ENSESTG00000005119 ENSESTT00000013106 Transcript intron_variant - - - - - - rs1860962 18:8199477 A 5797 NM_001105244.1 Transcript intron_variant - - - - - - rs1860962 18:8199477 A CCDS11840.1 CCDS11840.1 Transcript intron_variant - - - - - - rs1860962 18:8199477 A 5797 NM_002845.3 Transcript intron_variant - - - - - - rs1860962 18:8199477 A CCDS58613.1 CCDS58613.1 Transcript intron_variant - - - - - - rs6506571 18:8290218 G ENSESTG00000005119 ENSESTT00000013102 Transcript intron_variant - - - - - - rs6506571 18:8290218 G 5797 NM_001105244.1 Transcript intron_variant - - - - - - rs6506571 18:8290218 G CCDS11840.1 CCDS11840.1 Transcript intron_variant - - - - - - rs6506571 18:8290218 G 5797 NM_002845.3 Transcript intron_variant - - - - - - rs6506571 18:8290218 G CCDS58613.1 CCDS58613.1 Transcript intron_variant - - - - - - rs6506573 18:8305185 C ENSESTG00000005119 ENSESTT00000013102 Transcript intron_variant - - - - - - rs6506573 18:8305185 C 5797 NM_001105244.1 Transcript intron_variant - - - - - - rs6506573 18:8305185 C CCDS11840.1 CCDS11840.1 Transcript intron_variant - - - - - - rs6506573 18:8305185 C 5797 NM_002845.3 Transcript intron_variant - - - - - - rs6506573 18:8305185 C CCDS58613.1 CCDS58613.1 Transcript intron_variant - - - - - - rs1251849 18:8363495 C 100192426 NR_024419.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1251849 18:8363495 C ENSESTG00000005119 ENSESTT00000013102 Transcript intron_variant - - - - - - rs1251849 18:8363495 C ENSESTG00000005242 ENSESTT00000013320 Transcript intron_variant - - - - - - rs1251849 18:8363495 C 5797 NM_001105244.1 Transcript intron_variant - - - - - - rs1251849 18:8363495 C CCDS11840.1 CCDS11840.1 Transcript intron_variant - - - - - - rs1251849 18:8363495 C 5797 NM_002845.3 Transcript intron_variant - - - - - - rs1251849 18:8363495 C CCDS58613.1 CCDS58613.1 Transcript intron_variant - - - - - - rs2509541 18:8379650 G ENSESTG00000005119 ENSESTT00000013120 Transcript upstream_gene_variant - - - - - - DISTANCE=945 rs2509541 18:8379650 G ENSESTG00000005119 ENSESTT00000013118 Transcript upstream_gene_variant - - - - - - DISTANCE=639 rs2509541 18:8379650 G CCDS58613.1 CCDS58613.1 Transcript intron_variant - - - - - - rs2509541 18:8379650 G ENSESTG00000005119 ENSESTT00000013102 Transcript intron_variant - - - - - - rs2509541 18:8379650 G ENSESTG00000005119 ENSESTT00000013114 Transcript downstream_gene_variant - - - - - - DISTANCE=3008 rs2509541 18:8379650 G 5797 NM_001105244.1 Transcript intron_variant - - - - - - rs2509541 18:8379650 G CCDS11840.1 CCDS11840.1 Transcript intron_variant - - - - - - rs2509541 18:8379650 G 5797 NM_002845.3 Transcript intron_variant - - - - - - rs2509541 18:8379650 G ENSESTG00000005119 ENSESTT00000013117 Transcript intron_variant - - - - - - rs606994 18:8444530 G - - - intergenic_variant - - - - - - rs7343036 18:8542683 G - - - intergenic_variant - - - - - - rs329013 18:9506580 C - ENSR00000276494 RegulatoryFeature regulatory_region_variant - - - - - - rs329013 18:9506580 C ENSESTG00000021164 ENSESTT00000053126 Transcript intron_variant - - - - - - rs329013 18:9506580 C 10928 NM_006788.3 Transcript intron_variant - - - - - - rs7244072 18:9807825 A ENSESTG00000021267 ENSESTT00000053529 Transcript intron_variant - - - - - - rs7244072 18:9807825 A CCDS45826.1 CCDS45826.1 Transcript intron_variant - - - - - - rs7244072 18:9807825 A ENSESTG00000021267 ENSESTT00000053551 Transcript intron_variant - - - - - - rs7244072 18:9807825 A 11031 NM_006868.3 Transcript intron_variant - - - - - - rs629383 18:9992786 A - ENSR00000522228 RegulatoryFeature regulatory_region_variant - - - - - - rs629383 18:9992786 A - - - intergenic_variant - - - - - - rs490216 18:10111677 A - - - intergenic_variant - - - - - - rs9949268 18:10267232 G - - - intergenic_variant - - - - - - rs6505542 18:10286276 C - - - intergenic_variant - - - - - - rs206479 18:10294824 A - - - intergenic_variant - - - - - - rs206593 18:10340457 T ENSESTG00000022819 ENSESTT00000057520 Transcript upstream_gene_variant - - - - - - DISTANCE=1595 rs6505554 18:10435706 G - - - intergenic_variant - - - - - - rs206446 18:10440915 A - ENSR00001513190 RegulatoryFeature regulatory_region_variant - - - - - - rs206446 18:10440915 A - - - intergenic_variant - - - - - - rs206443 18:10441687 G - - - intergenic_variant - - - - - - rs206438 18:10444942 T - ENSR00000522312 RegulatoryFeature regulatory_region_variant - - - - - - rs206438 18:10444942 T - - - intergenic_variant - - - - - - rs688666 18:10611901 A ENSESTG00000022795 ENSESTT00000057501 Transcript downstream_gene_variant - - - - - - DISTANCE=572 rs519246 18:10639487 C - - - intergenic_variant - - - - - - rs2865131 18:10763218 C 63895 NM_022068.2 Transcript intron_variant - - - - - - rs2865131 18:10763218 C ENSESTG00000022708 ENSESTT00000057326 Transcript intron_variant - - - - - - rs2865131 18:10763218 C ENSESTG00000022741 ENSESTT00000057347 Transcript upstream_gene_variant - - - - - - DISTANCE=651 rs2865131 18:10763218 C ENSESTG00000022665 ENSESTT00000057175 Transcript intron_variant - - - - - - rs9945829 18:10813634 T 63895 NM_022068.2 Transcript intron_variant - - - - - - rs9945829 18:10813634 T ENSESTG00000022665 ENSESTT00000057175 Transcript intron_variant - - - - - - rs4414553 18:10950617 T 63895 NM_022068.2 Transcript intron_variant - - - - - - rs4414553 18:10950617 T ENSESTG00000022647 ENSESTT00000057153 Transcript intron_variant - - - - - - rs7228062 18:11177794 A - - - intergenic_variant - - - - - - rs11080498 18:11186079 A - - - intergenic_variant - - - - - - rs2030043 18:11192269 G - - - intergenic_variant - - - - - - rs7239226 18:11193903 C - - - intergenic_variant - - - - - - rs925035 18:11203604 G - - - intergenic_variant - - - - - - rs1874769 18:11218992 G - - - intergenic_variant - - - - - - rs11659696 18:11227691 A - - - intergenic_variant - - - - - - rs516087 18:11533116 C - - - intergenic_variant - - - - - - rs564525 18:11646469 G - - - intergenic_variant - - - - - - rs1382116 18:11649432 C - - - intergenic_variant - - - - - - rs6505667 18:11656250 A - - - intergenic_variant - - - - - - rs7505468 18:12319093 A - ENSR00000667670 RegulatoryFeature regulatory_region_variant - - - - - - rs7505468 18:12319093 A ENSESTG00000001419 ENSESTT00000003412 Transcript intron_variant - - - - - - rs7505468 18:12319093 A ENSESTG00000001610 ENSESTT00000003863 Transcript intron_variant - - - - - - rs7505468 18:12319093 A ENSESTG00000001419 ENSESTT00000003417 Transcript intron_variant - - - - - - rs7505468 18:12319093 A ENSESTG00000001419 ENSESTT00000003394 Transcript intron_variant - - - - - - rs7505468 18:12319093 A CCDS11858.1 CCDS11858.1 Transcript intron_variant - - - - - - rs7505468 18:12319093 A ENSESTG00000001610 ENSESTT00000003874 Transcript intron_variant - - - - - - rs7505468 18:12319093 A ENSESTG00000001610 ENSESTT00000003882 Transcript intron_variant - - - - - - rs7505468 18:12319093 A ENSESTG00000001419 ENSESTT00000003390 Transcript intron_variant - - - - - - rs7505468 18:12319093 A 84617 NM_032525.1 Transcript intron_variant - - - - - - rs7505468 18:12319093 A ENSESTG00000001419 ENSESTT00000003373 Transcript intron_variant - - - - - - rs7505468 18:12319093 A ENSESTG00000001419 ENSESTT00000003400 Transcript intron_variant - - - - - - rs1786519 18:13566177 G ENSESTG00000025132 ENSESTT00000063490 Transcript intron_variant - - - - - - rs1786519 18:13566177 G CCDS32793.1 CCDS32793.1 Transcript intron_variant - - - - - - rs1786519 18:13566177 G ENSESTG00000025132 ENSESTT00000063535 Transcript intron_variant - - - - - - rs1786519 18:13566177 G 753 NM_181482.3 Transcript intron_variant - - - - - - rs1786519 18:13566177 G 753 NM_181481.3 Transcript intron_variant - - - - - - rs1786519 18:13566177 G ENSESTG00000025132 ENSESTT00000063406 Transcript intron_variant - - - - - - rs1786519 18:13566177 G ENSESTG00000025132 ENSESTT00000063448 Transcript intron_variant - - - - - - rs1786519 18:13566177 G CCDS32794.1 CCDS32794.1 Transcript intron_variant - - - - - - rs1786519 18:13566177 G ENSESTG00000025132 ENSESTT00000063502 Transcript intron_variant - - - - - - rs1786519 18:13566177 G ENSESTG00000025132 ENSESTT00000063419 Transcript intron_variant - - - - - - rs1786519 18:13566177 G ENSESTG00000025132 ENSESTT00000063519 Transcript intron_variant - - - - - - rs1786519 18:13566177 G ENSESTG00000025132 ENSESTT00000063456 Transcript intron_variant - - - - - - rs288990 18:18613113 G ENSESTG00000002989 ENSESTT00000007550 Transcript intron_variant - - - - - - rs288990 18:18613113 G CCDS11870.2 CCDS11870.2 Transcript intron_variant - - - - - - rs288990 18:18613113 G ENSESTG00000002989 ENSESTT00000007578 Transcript intron_variant - - - - - - rs288990 18:18613113 G ENSESTG00000002989 ENSESTT00000007552 Transcript intron_variant - - - - - - rs288990 18:18613113 G ENSESTG00000002989 ENSESTT00000007561 Transcript intron_variant - - - - - - rs288990 18:18613113 G 6093 NM_005406.2 Transcript intron_variant - - - - - - rs288990 18:18613113 G ENSESTG00000002989 ENSESTT00000007555 Transcript intron_variant - - - - - - rs288990 18:18613113 G ENSESTG00000002989 ENSESTT00000007576 Transcript intron_variant - - - - - - rs288990 18:18613113 G ENSESTG00000002989 ENSESTT00000007573 Transcript intron_variant - - - - - - rs288990 18:18613113 G ENSESTG00000002989 ENSESTT00000007580 Transcript intron_variant - - - - - - rs4997366 18:19774308 G - ENSR00000276852 RegulatoryFeature regulatory_region_variant - - - - - - rs4997366 18:19774308 G ENSESTG00000006132 ENSESTT00000015461 Transcript intron_variant - - - - - - rs4997366 18:19774308 G CCDS11872.1 CCDS11872.1 Transcript intron_variant - - - - - - rs4997366 18:19774308 G 2627 NM_005257.4 Transcript intron_variant - - - - - - rs9957383 18:19848010 T ENSESTG00000034150 ENSESTT00000086304 Transcript intron_variant - - - - - - rs6507101 18:19881563 A - - - intergenic_variant - - - - - - rs4567841 18:20203972 G - - - intergenic_variant - - - - - - rs299249 18:20291115 T - ENSR00000523122 RegulatoryFeature regulatory_region_variant - - - - - - rs299249 18:20291115 T - - - intergenic_variant - - - - - - rs6507621 18:20964429 G 85019 NM_032933.4 Transcript intron_variant - - - - - - rs6507621 18:20964429 G ENSESTG00000033263 ENSESTT00000084063 Transcript intron_variant - - - - - - rs6507621 18:20964429 G ENSESTG00000033263 ENSESTT00000084072 Transcript intron_variant - - - - - - rs6507621 18:20964429 G ENSESTG00000033263 ENSESTT00000084093 Transcript intron_variant - - - - - - rs6507621 18:20964429 G CCDS11876.2 CCDS11876.2 Transcript intron_variant - - - - - - rs6507621 18:20964429 G ENSESTG00000033263 ENSESTT00000084055 Transcript intron_variant - - - - - - rs6507621 18:20964429 G ENSESTG00000033263 ENSESTT00000084067 Transcript intron_variant - - - - - - rs6507621 18:20964429 G ENSESTG00000033263 ENSESTT00000084084 Transcript intron_variant - - - - - - rs6507621 18:20964429 G ENSESTG00000033263 ENSESTT00000084028 Transcript intron_variant - - - - - - rs303759 18:21084098 C - ENSR00000276914 RegulatoryFeature regulatory_region_variant - - - - - - rs303759 18:21084098 C ENSESTG00000032837 ENSESTT00000083014 Transcript intron_variant - - - - - - rs303759 18:21084098 C CCDS32803.1 CCDS32803.1 Transcript intron_variant - - - - - - rs303759 18:21084098 C 29919 NM_013326.3 Transcript intron_variant - - - - - - rs303759 18:21084098 C ENSESTG00000032837 ENSESTT00000082984 Transcript intron_variant - - - - - - rs303759 18:21084098 C ENSESTG00000032837 ENSESTT00000082962 Transcript intron_variant - - - - - - rs1652381 18:21088081 C ENSESTG00000032837 ENSESTT00000083014 Transcript intron_variant - - - - - - rs1652381 18:21088081 C CCDS32803.1 CCDS32803.1 Transcript intron_variant - - - - - - rs1652381 18:21088081 C 29919 NM_013326.3 Transcript intron_variant - - - - - - rs1652381 18:21088081 C ENSESTG00000032837 ENSESTT00000082984 Transcript intron_variant - - - - - - rs1652381 18:21088081 C ENSESTG00000032837 ENSESTT00000082962 Transcript downstream_gene_variant - - - - - - DISTANCE=3395 rs891277 18:21483218 T - ENSR00000523379 RegulatoryFeature regulatory_region_variant - - - - - - rs891277 18:21483218 T ENSESTG00000032952 ENSESTT00000083398 Transcript intron_variant - - - - - - rs891277 18:21483218 T ENSESTG00000032952 ENSESTT00000083423 Transcript downstream_gene_variant - - - - - - DISTANCE=3559 rs891277 18:21483218 T CCDS42419.1 CCDS42419.1 Transcript intron_variant - - - - - - rs891277 18:21483218 T CCDS11880.1 CCDS11880.1 Transcript intron_variant - - - - - - rs891277 18:21483218 T ENSESTG00000032952 ENSESTT00000083407 Transcript intron_variant - - - - - - rs891277 18:21483218 T 3909 NM_000227.3 Transcript intron_variant - - - - - - rs891277 18:21483218 T 3909 NM_001127718.1 Transcript intron_variant - - - - - - rs891277 18:21483218 T 3909 NM_001127717.1 Transcript intron_variant - - - - - - rs891277 18:21483218 T 3909 NM_198129.1 Transcript intron_variant - - - - - - rs891277 18:21483218 T CCDS45838.1 CCDS45838.1 Transcript intron_variant - - - - - - rs891278 18:21489767 A - ENSR00000523385 RegulatoryFeature regulatory_region_variant - - - - - - rs891278 18:21489767 A ENSESTG00000032952 ENSESTT00000083398 Transcript intron_variant - - - - - - rs891278 18:21489767 A CCDS42419.1 CCDS42419.1 Transcript intron_variant - - - - - - rs891278 18:21489767 A CCDS11880.1 CCDS11880.1 Transcript intron_variant - - - - - - rs891278 18:21489767 A ENSESTG00000032952 ENSESTT00000083407 Transcript intron_variant - - - - - - rs891278 18:21489767 A 3909 NM_000227.3 Transcript intron_variant - - - - - - rs891278 18:21489767 A 3909 NM_001127718.1 Transcript intron_variant - - - - - - rs891278 18:21489767 A 3909 NM_001127717.1 Transcript intron_variant - - - - - - rs891278 18:21489767 A 3909 NM_198129.1 Transcript intron_variant - - - - - - rs891278 18:21489767 A CCDS45838.1 CCDS45838.1 Transcript intron_variant - - - - - - rs1258153 18:21507757 C - ENSR00000523405 RegulatoryFeature regulatory_region_variant - - - - - - rs1258153 18:21507757 C ENSESTG00000032952 ENSESTT00000083398 Transcript intron_variant - - - - - - rs1258153 18:21507757 C CCDS42419.1 CCDS42419.1 Transcript intron_variant - - - - - - rs1258153 18:21507757 C CCDS11880.1 CCDS11880.1 Transcript intron_variant - - - - - - rs1258153 18:21507757 C ENSESTG00000032952 ENSESTT00000083407 Transcript intron_variant - - - - - - rs1258153 18:21507757 C 3909 NM_000227.3 Transcript intron_variant - - - - - - rs1258153 18:21507757 C 3909 NM_001127718.1 Transcript intron_variant - - - - - - rs1258153 18:21507757 C 3909 NM_001127717.1 Transcript intron_variant - - - - - - rs1258153 18:21507757 C 3909 NM_198129.1 Transcript intron_variant - - - - - - rs1258153 18:21507757 C CCDS45838.1 CCDS45838.1 Transcript intron_variant - - - - - - rs1154233 18:21511089 G ENSESTG00000032952 ENSESTT00000083398 Transcript missense_variant 2950 2575 859 S/G Agc/Ggc - rs1154233 18:21511089 G CCDS42419.1 CCDS42419.1 Transcript missense_variant 8500 8500 2834 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs1154233 18:21511089 G CCDS11880.1 CCDS11880.1 Transcript missense_variant 3673 3673 1225 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs1154233 18:21511089 G ENSESTG00000032952 ENSESTT00000083407 Transcript missense_variant 2950 2575 859 S/G Agc/Ggc - rs1154233 18:21511089 G 3909 NM_000227.3 Transcript missense_variant 3698 3673 1225 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs1154233 18:21511089 G 3909 NM_001127718.1 Transcript missense_variant 3530 3505 1169 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs1154233 18:21511089 G 3909 NM_001127717.1 Transcript missense_variant 8418 8332 2778 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs1154233 18:21511089 G 3909 NM_198129.1 Transcript missense_variant 8586 8500 2834 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs1154233 18:21511089 G CCDS45838.1 CCDS45838.1 Transcript missense_variant 8332 8332 2778 S/G Agc/Ggc - PolyPhen=benign;SIFT=tolerated rs1154242 18:21529604 A - ENSR00000523424 RegulatoryFeature regulatory_region_variant - - - - - - rs1154242 18:21529604 A CCDS42419.1 CCDS42419.1 Transcript intron_variant - - - - - - rs1154242 18:21529604 A CCDS11880.1 CCDS11880.1 Transcript intron_variant - - - - - - rs1154242 18:21529604 A 3909 NM_000227.3 Transcript intron_variant - - - - - - rs1154242 18:21529604 A ENSESTG00000033006 ENSESTT00000083484 Transcript intron_variant - - - - - - rs1154242 18:21529604 A 3909 NM_001127718.1 Transcript intron_variant - - - - - - rs1154242 18:21529604 A 3909 NM_001127717.1 Transcript intron_variant - - - - - - rs1154242 18:21529604 A 3909 NM_198129.1 Transcript intron_variant - - - - - - rs1154242 18:21529604 A CCDS45838.1 CCDS45838.1 Transcript intron_variant - - - - - - rs9949873 18:21608011 G 125488 NM_001135993.1 Transcript intron_variant - - - - - - rs9949873 18:21608011 G ENSESTG00000033039 ENSESTT00000083549 Transcript intron_variant - - - - - - rs9949873 18:21608011 G ENSESTG00000033039 ENSESTT00000083556 Transcript intron_variant - - - - - - rs9949873 18:21608011 G CCDS45839.1 CCDS45839.1 Transcript intron_variant - - - - - - rs9949873 18:21608011 G 125488 NM_153211.3 Transcript intron_variant - - - - - - rs7237188 18:21623557 C 125488 NM_001135993.1 Transcript intron_variant - - - - - - rs7237188 18:21623557 C ENSESTG00000033039 ENSESTT00000083549 Transcript intron_variant - - - - - - rs7237188 18:21623557 C ENSESTG00000033039 ENSESTT00000083556 Transcript intron_variant - - - - - - rs7237188 18:21623557 C CCDS45839.1 CCDS45839.1 Transcript intron_variant - - - - - - rs7237188 18:21623557 C 125488 NM_153211.3 Transcript intron_variant - - - - - - rs1487437 18:21626302 A 125488 NM_001135993.1 Transcript intron_variant - - - - - - rs1487437 18:21626302 A ENSESTG00000033039 ENSESTT00000083549 Transcript intron_variant - - - - - - rs1487437 18:21626302 A ENSESTG00000033039 ENSESTT00000083556 Transcript intron_variant - - - - - - rs1487437 18:21626302 A CCDS45839.1 CCDS45839.1 Transcript intron_variant - - - - - - rs1487437 18:21626302 A 125488 NM_153211.3 Transcript intron_variant - - - - - - rs9955320 18:21664653 T ENSESTG00000033039 ENSESTT00000083549 Transcript intron_variant - - - - - - rs9955320 18:21664653 T ENSESTG00000033039 ENSESTT00000083556 Transcript downstream_gene_variant - - - - - - DISTANCE=1746 rs9955320 18:21664653 T CCDS45839.1 CCDS45839.1 Transcript intron_variant - - - - - - rs9955320 18:21664653 T ENSESTG00000033039 ENSESTT00000083566 Transcript downstream_gene_variant - - - - - - DISTANCE=1746 rs9955320 18:21664653 T 125488 NM_001135993.1 Transcript intron_variant - - - - - - rs9955320 18:21664653 T ENSESTG00000033039 ENSESTT00000083564 Transcript intron_variant - - - - - - rs9955320 18:21664653 T CCDS32804.1 CCDS32804.1 Transcript intron_variant - - - - - - rs9955320 18:21664653 T 125488 NM_153211.3 Transcript intron_variant - - - - - - rs1994421 18:21665145 C ENSESTG00000033039 ENSESTT00000083549 Transcript intron_variant - - - - - - rs1994421 18:21665145 C ENSESTG00000033039 ENSESTT00000083556 Transcript downstream_gene_variant - - - - - - DISTANCE=2238 rs1994421 18:21665145 C CCDS45839.1 CCDS45839.1 Transcript intron_variant - - - - - - rs1994421 18:21665145 C ENSESTG00000033039 ENSESTT00000083566 Transcript downstream_gene_variant - - - - - - DISTANCE=2238 rs1994421 18:21665145 C 125488 NM_001135993.1 Transcript intron_variant - - - - - - rs1994421 18:21665145 C ENSESTG00000033039 ENSESTT00000083564 Transcript intron_variant - - - - - - rs1994421 18:21665145 C CCDS32804.1 CCDS32804.1 Transcript intron_variant - - - - - - rs1994421 18:21665145 C 125488 NM_153211.3 Transcript intron_variant - - - - - - rs7231604 18:21690083 G ENSESTG00000033039 ENSESTT00000083549 Transcript intron_variant - - - - - - rs7231604 18:21690083 G ENSESTG00000033039 ENSESTT00000083571 Transcript upstream_gene_variant - - - - - - DISTANCE=3234 rs7231604 18:21690083 G CCDS45839.1 CCDS45839.1 Transcript intron_variant - - - - - - rs7231604 18:21690083 G 125488 NM_001135993.1 Transcript intron_variant - - - - - - rs7231604 18:21690083 G ENSESTG00000033039 ENSESTT00000083564 Transcript intron_variant - - - - - - rs7231604 18:21690083 G ENSESTG00000033039 ENSESTT00000083575 Transcript upstream_gene_variant - - - - - - DISTANCE=4221 rs7231604 18:21690083 G CCDS32804.1 CCDS32804.1 Transcript intron_variant - - - - - - rs7231604 18:21690083 G 125488 NM_153211.3 Transcript intron_variant - - - - - - rs4800176 18:21694618 A ENSESTG00000033039 ENSESTT00000083549 Transcript splice_region_variant,intron_variant - - - - - - rs4800176 18:21694618 A ENSESTG00000033039 ENSESTT00000083571 Transcript splice_region_variant,intron_variant - - - - - - rs4800176 18:21694618 A CCDS45839.1 CCDS45839.1 Transcript splice_region_variant,intron_variant - - - - - - rs4800176 18:21694618 A 125488 NM_001135993.1 Transcript splice_region_variant,intron_variant - - - - - - rs4800176 18:21694618 A ENSESTG00000033039 ENSESTT00000083564 Transcript splice_region_variant,intron_variant - - - - - - rs4800176 18:21694618 A ENSESTG00000033039 ENSESTT00000083575 Transcript 5_prime_UTR_variant 132 - - - - - rs4800176 18:21694618 A CCDS32804.1 CCDS32804.1 Transcript splice_region_variant,intron_variant - - - - - - rs4800176 18:21694618 A 125488 NM_153211.3 Transcript splice_region_variant,intron_variant - - - - - - rs11082965 18:21720252 A ENSESTG00000033115 ENSESTT00000083739 Transcript intron_variant - - - - - - rs11082965 18:21720252 A CCDS11882.1 CCDS11882.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2827 rs11082965 18:21720252 A CCDS11881.1 CCDS11881.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2827 rs11082965 18:21720252 A ENSESTG00000033115 ENSESTT00000083737 Transcript intron_variant - - - - - - rs11082965 18:21720252 A 26256 NM_153770.1 Transcript intron_variant - - - - - - rs11082965 18:21720252 A 26256 NM_153769.1 Transcript intron_variant - - - - - - rs11082965 18:21720252 A ENSESTG00000033105 ENSESTT00000083640 Transcript downstream_gene_variant - - - - - - DISTANCE=4686 rs11082965 18:21720252 A ENSESTG00000033115 ENSESTT00000083711 Transcript intron_variant - - - - - - rs11082965 18:21720252 A ENSESTG00000033115 ENSESTT00000083667 Transcript intron_variant - - - - - - rs11082965 18:21720252 A 125488 NM_153211.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4678 rs11082965 18:21720252 A CCDS42420.1 CCDS42420.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2827 rs11082965 18:21720252 A ENSESTG00000033115 ENSESTT00000083726 Transcript intron_variant - - - - - - rs11082965 18:21720252 A 26256 NM_153768.1 Transcript intron_variant - - - - - - rs11082965 18:21720252 A 26256 NM_012189.2 Transcript intron_variant - - - - - - rs11082965 18:21720252 A ENSESTG00000033115 ENSESTT00000083727 Transcript intron_variant - - - - - - rs11082965 18:21720252 A 26256 NM_138644.1 Transcript intron_variant - - - - - - rs11082965 18:21720252 A ENSESTG00000033115 ENSESTT00000083706 Transcript intron_variant - - - - - - rs11082965 18:21720252 A 125488 NM_001135993.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4678 rs11082965 18:21720252 A CCDS45840.1 CCDS45840.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2827 rs11082965 18:21720252 A ENSESTG00000033115 ENSESTT00000083697 Transcript intron_variant - - - - - - rs11082965 18:21720252 A ENSESTG00000033115 ENSESTT00000083716 Transcript intron_variant - - - - - - rs11082965 18:21720252 A 26256 NM_138643.1 Transcript intron_variant - - - - - - rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083739 Transcript downstream_gene_variant - - - - - - DISTANCE=2898 rs894926 18:21738965 G CCDS11882.1 CCDS11882.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2018 rs894926 18:21738965 G CCDS11881.1 CCDS11881.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2018 rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083737 Transcript intron_variant - - - - - - rs894926 18:21738965 G 114876 NM_001242508.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3044 rs894926 18:21738965 G ENSESTG00000033157 ENSESTT00000083769 Transcript downstream_gene_variant - - - - - - DISTANCE=3996 rs894926 18:21738965 G 26256 NM_153770.1 Transcript intron_variant - - - - - - rs894926 18:21738965 G 26256 NM_153769.1 Transcript intron_variant - - - - - - rs894926 18:21738965 G 114876 NM_080597.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3044 rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083711 Transcript intron_variant - - - - - - rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083667 Transcript downstream_gene_variant - - - - - - DISTANCE=2840 rs894926 18:21738965 G CCDS42420.1 CCDS42420.1 Transcript intron_variant - - - - - - rs894926 18:21738965 G CCDS11883.1 CCDS11883.1 Transcript intron_variant - - - - - - rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083726 Transcript downstream_gene_variant - - - - - - DISTANCE=2952 rs894926 18:21738965 G CCDS11884.1 CCDS11884.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4178 rs894926 18:21738965 G 26256 NM_153768.1 Transcript intron_variant - - - - - - rs894926 18:21738965 G 26256 NM_012189.2 Transcript intron_variant - - - - - - rs894926 18:21738965 G CCDS56056.1 CCDS56056.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4178 rs894926 18:21738965 G CCDS11885.1 CCDS11885.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4178 rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083727 Transcript downstream_gene_variant - - - - - - DISTANCE=2898 rs894926 18:21738965 G 26256 NM_138644.1 Transcript intron_variant - - - - - - rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083751 Transcript upstream_gene_variant - - - - - - DISTANCE=564 rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083706 Transcript intron_variant - - - - - - rs894926 18:21738965 G 114876 NM_018030.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3044 rs894926 18:21738965 G CCDS45840.1 CCDS45840.1 Transcript intron_variant - - - - - - rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083697 Transcript intron_variant - - - - - - rs894926 18:21738965 G ENSESTG00000033115 ENSESTT00000083716 Transcript downstream_gene_variant - - - - - - DISTANCE=2898 rs894926 18:21738965 G 26256 NM_138643.1 Transcript intron_variant - - - - - - rs275863 18:21830057 C CCDS11884.1 CCDS11884.1 Transcript intron_variant - - - - - - rs275863 18:21830057 C ENSESTG00000034747 ENSESTT00000087895 Transcript intron_variant - - - - - - rs275863 18:21830057 C ENSESTG00000034747 ENSESTT00000087889 Transcript intron_variant - - - - - - rs275863 18:21830057 C CCDS56056.1 CCDS56056.1 Transcript intron_variant - - - - - - rs275863 18:21830057 C ENSESTG00000034747 ENSESTT00000087891 Transcript intron_variant - - - - - - rs275863 18:21830057 C ENSESTG00000034747 ENSESTT00000087899 Transcript intron_variant - - - - - - rs275863 18:21830057 C 114876 NM_001242508.1 Transcript intron_variant - - - - - - rs275863 18:21830057 C 114876 NM_018030.4 Transcript intron_variant - - - - - - rs275863 18:21830057 C ENSESTG00000034747 ENSESTT00000087885 Transcript intron_variant - - - - - - rs275863 18:21830057 C ENSESTG00000034747 ENSESTT00000087897 Transcript intron_variant - - - - - - rs275863 18:21830057 C 114876 NM_080597.3 Transcript intron_variant - - - - - - rs275863 18:21830057 C ENSESTG00000034747 ENSESTT00000087881 Transcript intron_variant - - - - - - rs695049 18:22012999 G 55364 NM_018439.3 Transcript intron_variant - - - - - - rs695049 18:22012999 G CCDS11886.1 CCDS11886.1 Transcript intron_variant - - - - - - rs695049 18:22012999 G ENSESTG00000034701 ENSESTT00000087761 Transcript intron_variant - - - - - - rs1791507 18:22133747 G - ENSR00000523519 RegulatoryFeature regulatory_region_variant - - - - - - rs1791507 18:22133747 G - - - intergenic_variant - - - - - - rs4306594 18:22679942 C - ENSR00000523590 RegulatoryFeature regulatory_region_variant - - - - - - rs4306594 18:22679942 C ENSESTG00000034733 ENSESTT00000087809 Transcript intron_variant - - - - - - rs4306594 18:22679942 C CCDS32806.1 CCDS32806.1 Transcript intron_variant - - - - - - rs4306594 18:22679942 C 25925 NM_015461.2 Transcript intron_variant - - - - - - rs7232219 18:22871737 G ENSESTG00000034782 ENSESTT00000087941 Transcript intron_variant - - - - - - rs7232219 18:22871737 G ENSESTG00000034782 ENSESTT00000087930 Transcript intron_variant - - - - - - rs7232219 18:22871737 G CCDS32806.1 CCDS32806.1 Transcript intron_variant - - - - - - rs7232219 18:22871737 G 25925 NM_015461.2 Transcript intron_variant - - - - - - rs7232219 18:22871737 G ENSESTG00000034782 ENSESTT00000087934 Transcript intron_variant - - - - - - rs7232219 18:22871737 G ENSESTG00000034782 ENSESTT00000087922 Transcript intron_variant - - - - - - rs7232219 18:22871737 G ENSESTG00000034782 ENSESTT00000087925 Transcript intron_variant - - - - - - rs7237479 18:22897820 C ENSESTG00000034782 ENSESTT00000087941 Transcript intron_variant - - - - - - rs7237479 18:22897820 C ENSESTG00000034782 ENSESTT00000087930 Transcript intron_variant - - - - - - rs7237479 18:22897820 C CCDS32806.1 CCDS32806.1 Transcript intron_variant - - - - - - rs7237479 18:22897820 C 25925 NM_015461.2 Transcript intron_variant - - - - - - rs7237479 18:22897820 C ENSESTG00000034782 ENSESTT00000087934 Transcript intron_variant - - - - - - rs7237479 18:22897820 C ENSESTG00000034782 ENSESTT00000087922 Transcript intron_variant - - - - - - rs7237479 18:22897820 C ENSESTG00000034782 ENSESTT00000087925 Transcript intron_variant - - - - - - rs4800218 18:23085759 A - - - intergenic_variant - - - - - - rs1785751 18:23504671 A - - - intergenic_variant - - - - - - rs674705 18:23617858 A CCDS54183.1 CCDS54183.1 Transcript intron_variant - - - - - - rs674705 18:23617858 A 6760 NM_005637.2 Transcript intron_variant - - - - - - rs674705 18:23617858 A ENSESTG00000034761 ENSESTT00000087907 Transcript downstream_gene_variant - - - - - - DISTANCE=661 rs674705 18:23617858 A CCDS32807.1 CCDS32807.1 Transcript intron_variant - - - - - - rs674705 18:23617858 A 6760 NM_001007559.1 Transcript intron_variant - - - - - - rs4459630 18:24021130 T - ENSR00001513776 RegulatoryFeature regulatory_region_variant - - - - - - rs4459630 18:24021130 T - - - intergenic_variant - - - - - - rs477923 18:24201699 C - ENSR00000523748 RegulatoryFeature regulatory_region_variant - - - - - - rs477923 18:24201699 C 284252 NM_001258222.1 Transcript intron_variant - - - - - - rs477923 18:24201699 C 284252 NM_198991.3 Transcript intron_variant - - - - - - rs477923 18:24201699 C ENSESTG00000005380 ENSESTT00000013677 Transcript intron_variant - - - - - - rs7504359 18:24223482 G 284252 NM_001258222.1 Transcript intron_variant - - - - - - rs7504359 18:24223482 G 284252 NM_198991.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3174 rs7504359 18:24223482 G ENSESTG00000005380 ENSESTT00000013677 Transcript intron_variant - - - - - - rs232355 18:24491080 C 147429 NR_026908.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs232355 18:24491080 C 83539 NM_031422.5 Transcript downstream_gene_variant - - - - - - DISTANCE=4515 rs232355 18:24491080 C 83539 NM_001256316.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4515 rs338063 18:24535299 G ENSESTG00000005331 ENSESTT00000013565 Transcript intron_variant - - - - - - rs338063 18:24535299 G 83539 NM_031422.5 Transcript intron_variant - - - - - - rs338063 18:24535299 G 83539 NM_001256316.1 Transcript intron_variant - - - - - - rs338063 18:24535299 G ENSESTG00000005331 ENSESTT00000013559 Transcript intron_variant - - - - - - rs338063 18:24535299 G CCDS58618.1 CCDS58618.1 Transcript intron_variant - - - - - - rs338063 18:24535299 G CCDS42422.1 CCDS42422.1 Transcript intron_variant - - - - - - rs1154213 18:24560646 C ENSESTG00000005331 ENSESTT00000013565 Transcript intron_variant - - - - - - rs1154213 18:24560646 C 83539 NM_031422.5 Transcript intron_variant - - - - - - rs1154213 18:24560646 C 83539 NM_001256316.1 Transcript intron_variant - - - - - - rs1154213 18:24560646 C ENSESTG00000005331 ENSESTT00000013559 Transcript intron_variant - - - - - - rs1154213 18:24560646 C CCDS58618.1 CCDS58618.1 Transcript intron_variant - - - - - - rs1154213 18:24560646 C CCDS42422.1 CCDS42422.1 Transcript intron_variant - - - - - - rs2617940 18:25300275 A - - - intergenic_variant - - - - - - rs2714367 18:25330261 A - ENSR00000667823 RegulatoryFeature regulatory_region_variant - - - - - - rs2714367 18:25330261 A - - - intergenic_variant - - - - - - rs1231237 18:25717622 C CCDS11891.1 CCDS11891.1 Transcript intron_variant - - - - - - rs1231237 18:25717622 C 1000 NM_001792.3 Transcript intron_variant - - - - - - rs1231237 18:25717622 C ENSESTG00000008619 ENSESTT00000021701 Transcript intron_variant - - - - - - rs7227854 18:25856288 T - - - intergenic_variant - - - - - - rs4553703 18:26176998 G - - - intergenic_variant - - - - - - rs1631466 18:26259989 G - - - intergenic_variant - - - - - - rs8091403 18:26361536 T - - - intergenic_variant - - - - - - rs552041 18:26461249 A - - - intergenic_variant - - - - - - rs476127 18:26470900 C - - - intergenic_variant - - - - - - rs6508575 18:26703040 A - - - intergenic_variant - - - - - - rs1960069 18:26704779 G - - - intergenic_variant - - - - - - rs1813471 18:26740297 T - - - intergenic_variant - - - - - - rs4361011 18:26804296 G - - - intergenic_variant - - - - - - rs1040136 18:26884132 G - - - intergenic_variant - - - - - - rs2037104 18:26922559 C - - - intergenic_variant - - - - - - rs1609363 18:26923893 T - - - intergenic_variant - - - - - - rs1849884 18:26938760 G - - - intergenic_variant - - - - - - rs7233079 18:27355768 A - - - intergenic_variant - - - - - - rs1583857 18:27395823 A - - - intergenic_variant - - - - - - rs4552087 18:27786334 G - - - intergenic_variant - - - - - - rs6508653 18:27818691 G - - - intergenic_variant - - - - - - rs9959271 18:27830329 T - - - intergenic_variant - - - - - - rs2850281 18:28283094 G - - - intergenic_variant - - - - - - rs2156474 18:28343503 G - - - intergenic_variant - - - - - - rs276936 18:28611139 C - ENSR00000277036 RegulatoryFeature regulatory_region_variant - - - - - - rs276936 18:28611139 C ENSESTG00000023253 ENSESTT00000058746 Transcript splice_acceptor_variant - - - - - - rs276936 18:28611139 C 1825 NM_024423.2 Transcript splice_acceptor_variant - - - - - - rs276936 18:28611139 C 1825 NM_001941.3 Transcript splice_acceptor_variant - - - - - - rs276936 18:28611139 C CCDS32810.1 CCDS32810.1 Transcript splice_acceptor_variant - - - - - - rs2912329 18:28905730 G CCDS11896.1 CCDS11896.1 Transcript intron_variant - - - - - - rs2912329 18:28905730 G ENSESTG00000022561 ENSESTT00000056994 Transcript upstream_gene_variant - - - - - - DISTANCE=1163 rs2912329 18:28905730 G ENSESTG00000022561 ENSESTT00000056975 Transcript intron_variant - - - - - - rs2912329 18:28905730 G 1828 NM_001942.2 Transcript intron_variant - - - - - - rs1941191 18:29044787 C - ENSR00001514017 RegulatoryFeature regulatory_region_variant - - - - - - rs1941191 18:29044787 C ENSESTG00000022677 ENSESTT00000057281 Transcript upstream_gene_variant - - - - - - DISTANCE=586 rs1941191 18:29044787 C CCDS11898.1 CCDS11898.1 Transcript intron_variant - - - - - - rs1941191 18:29044787 C ENSESTG00000022561 ENSESTT00000056994 Transcript intron_variant - - - - - - rs1941191 18:29044787 C 1830 NM_001944.2 Transcript intron_variant - - - - - - rs546351 18:29393780 G - - - intergenic_variant - - - - - - rs7234523 18:29417259 G CCDS11901.1 CCDS11901.1 Transcript intron_variant - - - - - - rs7234523 18:29417259 G ENSESTG00000023453 ENSESTT00000059244 Transcript intron_variant - - - - - - rs7234523 18:29417259 G ENSESTG00000023453 ENSESTT00000059203 Transcript intron_variant - - - - - - rs7234523 18:29417259 G 22878 NM_014939.3 Transcript intron_variant - - - - - - rs12964601 18:29465854 A ENSESTG00000022973 ENSESTT00000058081 Transcript intron_variant - - - - - - rs12964601 18:29465854 A CCDS11901.1 CCDS11901.1 Transcript intron_variant - - - - - - rs12964601 18:29465854 A 22878 NM_014939.3 Transcript intron_variant - - - - - - rs12964601 18:29465854 A ENSESTG00000022973 ENSESTT00000058099 Transcript intron_variant - - - - - - rs12964601 18:29465854 A ENSESTG00000022973 ENSESTT00000058069 Transcript intron_variant - - - - - - rs4799625 18:29604041 T ENSESTG00000022900 ENSESTT00000057803 Transcript intron_variant - - - - - - rs4799625 18:29604041 T ENSESTG00000022900 ENSESTT00000057780 Transcript intron_variant - - - - - - rs4799625 18:29604041 T 54941 NM_017831.3 Transcript intron_variant - - - - - - rs4799625 18:29604041 T ENSESTG00000022900 ENSESTT00000057791 Transcript intron_variant - - - - - - rs4799625 18:29604041 T CCDS11902.1 CCDS11902.1 Transcript intron_variant - - - - - - rs1458859 18:29952045 T - ENSR00001514084 RegulatoryFeature regulatory_region_variant - - - - - - rs1458859 18:29952045 T 64762 NM_022751.2 Transcript intron_variant - - - - - - rs1458859 18:29952045 T ENSESTG00000008782 ENSESTT00000022064 Transcript intron_variant - - - - - - rs1458859 18:29952045 T CCDS11905.1 CCDS11905.1 Transcript intron_variant - - - - - - rs1458859 18:29952045 T 64762 NM_001242409.1 Transcript intron_variant - - - - - - rs1458859 18:29952045 T CCDS56057.1 CCDS56057.1 Transcript intron_variant - - - - - - rs6506995 18:30485545 C - - - intergenic_variant - - - - - - rs1941285 18:30491818 G - ENSR00001514117 RegulatoryFeature regulatory_region_variant - - - - - - rs1941285 18:30491818 G - - - intergenic_variant - - - - - - rs11662808 18:30603161 T CCDS11906.1 CCDS11906.1 Transcript intron_variant - - - - - - rs11662808 18:30603161 T 374864 NM_001105528.1 Transcript intron_variant - - - - - - rs11662808 18:30603161 T CCDS42424.1 CCDS42424.1 Transcript intron_variant - - - - - - rs11662808 18:30603161 T 374864 NM_198995.2 Transcript intron_variant - - - - - - rs11662808 18:30603161 T ENSESTG00000008768 ENSESTT00000022008 Transcript intron_variant - - - - - - rs414674 18:30691786 A CCDS11906.1 CCDS11906.1 Transcript intron_variant - - - - - - rs414674 18:30691786 A 374864 NM_001105528.1 Transcript intron_variant - - - - - - rs414674 18:30691786 A CCDS42424.1 CCDS42424.1 Transcript intron_variant - - - - - - rs414674 18:30691786 A 374864 NM_198995.2 Transcript intron_variant - - - - - - rs414674 18:30691786 A ENSESTG00000008768 ENSESTT00000022008 Transcript intron_variant - - - - - - rs414674 18:30691786 A ENSESTG00000000295 ENSESTT00000000718 Transcript intron_variant - - - - - - rs8099648 18:30897949 C CCDS11906.1 CCDS11906.1 Transcript intron_variant - - - - - - rs8099648 18:30897949 C 374864 NM_001105528.1 Transcript intron_variant - - - - - - rs8099648 18:30897949 C CCDS42424.1 CCDS42424.1 Transcript intron_variant - - - - - - rs8099648 18:30897949 C 374864 NM_198995.2 Transcript intron_variant - - - - - - rs11661826 18:31177587 C ENSESTG00000000272 ENSESTT00000000666 Transcript intron_variant - - - - - - rs11661826 18:31177587 C 80816 NM_030632.1 Transcript intron_variant - - - - - - rs11661826 18:31177587 C CCDS45847.1 CCDS45847.1 Transcript intron_variant - - - - - - rs11661826 18:31177587 C ENSESTG00000000272 ENSESTT00000000670 Transcript intron_variant - - - - - - rs11661826 18:31177587 C ENSESTG00000000272 ENSESTT00000000665 Transcript intron_variant - - - - - - rs11661826 18:31177587 C ENSESTG00000000272 ENSESTT00000000668 Transcript intron_variant - - - - - - rs11661826 18:31177587 C ENSESTG00000000272 ENSESTT00000000672 Transcript intron_variant - - - - - - rs1941703 18:31235552 A ENSESTG00000000272 ENSESTT00000000666 Transcript intron_variant - - - - - - rs1941703 18:31235552 A 80816 NM_030632.1 Transcript intron_variant - - - - - - rs1941703 18:31235552 A ENSESTG00000000272 ENSESTT00000000677 Transcript intron_variant - - - - - - rs1941703 18:31235552 A CCDS45847.1 CCDS45847.1 Transcript intron_variant - - - - - - rs1941703 18:31235552 A ENSESTG00000000272 ENSESTT00000000665 Transcript intron_variant - - - - - - rs1941703 18:31235552 A ENSESTG00000000272 ENSESTT00000000668 Transcript intron_variant - - - - - - rs1941703 18:31235552 A ENSESTG00000000272 ENSESTT00000000672 Transcript intron_variant - - - - - - rs9965823 18:31253152 G ENSESTG00000000272 ENSESTT00000000666 Transcript intron_variant - - - - - - rs9965823 18:31253152 G 80816 NM_030632.1 Transcript intron_variant - - - - - - rs9965823 18:31253152 G ENSESTG00000000272 ENSESTT00000000677 Transcript intron_variant - - - - - - rs9965823 18:31253152 G CCDS45847.1 CCDS45847.1 Transcript intron_variant - - - - - - rs9965823 18:31253152 G ENSESTG00000000272 ENSESTT00000000665 Transcript intron_variant - - - - - - rs9965823 18:31253152 G ENSESTG00000000272 ENSESTT00000000668 Transcript intron_variant - - - - - - rs9965823 18:31253152 G ENSESTG00000000272 ENSESTT00000000672 Transcript intron_variant - - - - - - rs3859352 18:31277531 C ENSESTG00000000272 ENSESTT00000000666 Transcript intron_variant - - - - - - rs3859352 18:31277531 C 80816 NM_030632.1 Transcript intron_variant - - - - - - rs3859352 18:31277531 C ENSESTG00000000272 ENSESTT00000000677 Transcript intron_variant - - - - - - rs3859352 18:31277531 C CCDS45847.1 CCDS45847.1 Transcript intron_variant - - - - - - rs3859352 18:31277531 C ENSESTG00000000272 ENSESTT00000000665 Transcript intron_variant - - - - - - rs3859352 18:31277531 C ENSESTG00000000272 ENSESTT00000000668 Transcript intron_variant - - - - - - rs3859352 18:31277531 C ENSESTG00000000272 ENSESTT00000000672 Transcript intron_variant - - - - - - rs1353169 18:31342122 T - - - intergenic_variant - - - - - - rs11876573 18:31389489 C - - - intergenic_variant - - - - - - rs1597848 18:31501557 G 8715 NM_001198548.1 Transcript intron_variant - - - - - - rs1597848 18:31501557 G ENSESTG00000000282 ENSESTT00000000699 Transcript intron_variant - - - - - - rs1597848 18:31501557 G 8715 NR_036752.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1597848 18:31501557 G CCDS56058.1 CCDS56058.1 Transcript intron_variant - - - - - - rs1597848 18:31501557 G 8715 NM_001198549.1 Transcript intron_variant - - - - - - rs1597848 18:31501557 G 8715 NM_001198546.1 Transcript intron_variant - - - - - - rs1597848 18:31501557 G ENSESTG00000000282 ENSESTT00000000697 Transcript intron_variant - - - - - - rs1597848 18:31501557 G 8715 NM_001198547.1 Transcript intron_variant - - - - - - rs1597848 18:31501557 G ENSESTG00000000282 ENSESTT00000000701 Transcript intron_variant - - - - - - rs1597848 18:31501557 G CCDS11907.2 CCDS11907.2 Transcript intron_variant - - - - - - rs1597848 18:31501557 G ENSESTG00000000282 ENSESTT00000000702 Transcript intron_variant - - - - - - rs1597848 18:31501557 G CCDS56059.1 CCDS56059.1 Transcript intron_variant - - - - - - rs1597848 18:31501557 G 8715 NM_003787.4 Transcript intron_variant - - - - - - rs1941351 18:31523457 A 8715 NM_001198548.1 Transcript intron_variant - - - - - - rs1941351 18:31523457 A ENSESTG00000000282 ENSESTT00000000699 Transcript intron_variant - - - - - - rs1941351 18:31523457 A 8715 NR_036752.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1941351 18:31523457 A CCDS56058.1 CCDS56058.1 Transcript intron_variant - - - - - - rs1941351 18:31523457 A 8715 NM_001198549.1 Transcript intron_variant - - - - - - rs1941351 18:31523457 A 8715 NM_001198546.1 Transcript intron_variant - - - - - - rs1941351 18:31523457 A ENSESTG00000000282 ENSESTT00000000697 Transcript intron_variant - - - - - - rs1941351 18:31523457 A 8715 NM_001198547.1 Transcript intron_variant - - - - - - rs1941351 18:31523457 A ENSESTG00000000282 ENSESTT00000000701 Transcript intron_variant - - - - - - rs1941351 18:31523457 A CCDS11907.2 CCDS11907.2 Transcript intron_variant - - - - - - rs1941351 18:31523457 A ENSESTG00000000282 ENSESTT00000000702 Transcript intron_variant - - - - - - rs1941351 18:31523457 A CCDS56059.1 CCDS56059.1 Transcript intron_variant - - - - - - rs1941351 18:31523457 A 8715 NM_003787.4 Transcript intron_variant - - - - - - rs1597849 18:31553068 G 8715 NM_001198548.1 Transcript intron_variant - - - - - - rs1597849 18:31553068 G ENSESTG00000000282 ENSESTT00000000699 Transcript intron_variant - - - - - - rs1597849 18:31553068 G 8715 NR_036752.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1597849 18:31553068 G CCDS56058.1 CCDS56058.1 Transcript intron_variant - - - - - - rs1597849 18:31553068 G 8715 NM_001198549.1 Transcript intron_variant - - - - - - rs1597849 18:31553068 G 8715 NM_001198546.1 Transcript intron_variant - - - - - - rs1597849 18:31553068 G ENSESTG00000000282 ENSESTT00000000697 Transcript intron_variant - - - - - - rs1597849 18:31553068 G 8715 NM_001198547.1 Transcript intron_variant - - - - - - rs1597849 18:31553068 G ENSESTG00000000282 ENSESTT00000000701 Transcript intron_variant - - - - - - rs1597849 18:31553068 G CCDS11907.2 CCDS11907.2 Transcript intron_variant - - - - - - rs1597849 18:31553068 G CCDS56059.1 CCDS56059.1 Transcript intron_variant - - - - - - rs1597849 18:31553068 G 8715 NM_003787.4 Transcript intron_variant - - - - - - rs8085821 18:31613442 C 8715 NM_001198548.1 Transcript intron_variant - - - - - - rs8085821 18:31613442 C ENSESTG00000000282 ENSESTT00000000699 Transcript intron_variant - - - - - - rs8085821 18:31613442 C 8715 NR_036752.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8085821 18:31613442 C 8715 NM_001198549.1 Transcript intron_variant - - - - - - rs8085821 18:31613442 C 8715 NM_001198546.1 Transcript intron_variant - - - - - - rs8085821 18:31613442 C ENSESTG00000000282 ENSESTT00000000697 Transcript intron_variant - - - - - - rs8085821 18:31613442 C 8715 NM_001198547.1 Transcript intron_variant - - - - - - rs8085821 18:31613442 C ENSESTG00000000282 ENSESTT00000000701 Transcript intron_variant - - - - - - rs8085821 18:31613442 C CCDS11907.2 CCDS11907.2 Transcript intron_variant - - - - - - rs8085821 18:31613442 C CCDS56059.1 CCDS56059.1 Transcript intron_variant - - - - - - rs8085821 18:31613442 C 8715 NM_003787.4 Transcript intron_variant - - - - - - rs9965274 18:31642066 T 8715 NM_001198548.1 Transcript intron_variant - - - - - - rs9965274 18:31642066 T ENSESTG00000000282 ENSESTT00000000699 Transcript intron_variant - - - - - - rs9965274 18:31642066 T 8715 NR_036752.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9965274 18:31642066 T 8715 NM_001198546.1 Transcript intron_variant - - - - - - rs9965274 18:31642066 T 8715 NM_001198547.1 Transcript intron_variant - - - - - - rs9965274 18:31642066 T ENSESTG00000000282 ENSESTT00000000697 Transcript intron_variant - - - - - - rs9965274 18:31642066 T CCDS11907.2 CCDS11907.2 Transcript intron_variant - - - - - - rs9965274 18:31642066 T CCDS56059.1 CCDS56059.1 Transcript intron_variant - - - - - - rs9965274 18:31642066 T 8715 NM_003787.4 Transcript intron_variant - - - - - - rs9954798 18:31702641 A - ENSR00001514154 RegulatoryFeature regulatory_region_variant - - - - - - rs9954798 18:31702641 A 8715 NM_001198548.1 Transcript intron_variant - - - - - - rs9954798 18:31702641 A 8715 NR_036752.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9954798 18:31702641 A 8715 NM_001198546.1 Transcript intron_variant - - - - - - rs9954798 18:31702641 A ENSESTG00000026645 ENSESTT00000067150 Transcript intron_variant - - - - - - rs9954798 18:31702641 A 8715 NM_001198547.1 Transcript intron_variant - - - - - - rs9954798 18:31702641 A ENSESTG00000000282 ENSESTT00000000697 Transcript intron_variant - - - - - - rs9954798 18:31702641 A CCDS11907.2 CCDS11907.2 Transcript intron_variant - - - - - - rs9954798 18:31702641 A ENSESTG00000026645 ENSESTT00000067100 Transcript intron_variant - - - - - - rs9954798 18:31702641 A CCDS56059.1 CCDS56059.1 Transcript intron_variant - - - - - - rs9954798 18:31702641 A 8715 NM_003787.4 Transcript intron_variant - - - - - - rs2509593 18:32081021 G ENSESTG00000026336 ENSESTT00000066657 Transcript intron_variant - - - - - - rs2509593 18:32081021 G ENSESTG00000026336 ENSESTT00000066587 Transcript intron_variant - - - - - - rs2509593 18:32081021 G ENSESTG00000026336 ENSESTT00000066667 Transcript intron_variant - - - - - - rs2509593 18:32081021 G 1837 NM_032975.3 Transcript intron_variant - - - - - - rs2509593 18:32081021 G 1837 NM_001392.4 Transcript intron_variant - - - - - - rs2509593 18:32081021 G 1837 NM_001198945.1 Transcript intron_variant - - - - - - rs2509593 18:32081021 G 1837 NM_032979.4 Transcript intron_variant - - - - - - rs1898785 18:32220827 A ENSESTG00000026336 ENSESTT00000066684 Transcript intron_variant - - - - - - rs1898785 18:32220827 A ENSESTG00000026336 ENSESTT00000066657 Transcript intron_variant - - - - - - rs1898785 18:32220827 A 1837 NM_001198940.1 Transcript intron_variant - - - - - - rs1898785 18:32220827 A ENSESTG00000026336 ENSESTT00000066587 Transcript intron_variant - - - - - - rs1898785 18:32220827 A ENSESTG00000026336 ENSESTT00000066667 Transcript intron_variant - - - - - - rs1898785 18:32220827 A 1837 NM_001128175.1 Transcript intron_variant - - - - - - rs1898785 18:32220827 A 1837 NM_032975.3 Transcript intron_variant - - - - - - rs1898785 18:32220827 A 1837 NM_001392.4 Transcript intron_variant - - - - - - rs1898785 18:32220827 A 1837 NM_001198938.1 Transcript intron_variant - - - - - - rs1898785 18:32220827 A 1837 NM_032979.4 Transcript intron_variant - - - - - - rs1898785 18:32220827 A 1837 NM_001198945.1 Transcript intron_variant - - - - - - rs1898785 18:32220827 A 1837 NM_001198939.1 Transcript intron_variant - - - - - - rs531540 18:32635073 T CCDS58619.1 CCDS58619.1 Transcript intron_variant - - - - - - rs531540 18:32635073 T 10982 NR_046177.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs531540 18:32635073 T ENSESTG00000026580 ENSESTT00000067010 Transcript intron_variant - - - - - - rs531540 18:32635073 T 10982 NM_014268.3 Transcript intron_variant - - - - - - rs531540 18:32635073 T 10982 NM_001143826.2 Transcript intron_variant - - - - - - rs531540 18:32635073 T 10982 NM_001256420.1 Transcript intron_variant - - - - - - rs531540 18:32635073 T 10982 NM_001143827.2 Transcript intron_variant - - - - - - rs531540 18:32635073 T CCDS45850.1 CCDS45850.1 Transcript intron_variant - - - - - - rs531540 18:32635073 T CCDS11910.1 CCDS11910.1 Transcript intron_variant - - - - - - rs531540 18:32635073 T ENSESTG00000026580 ENSESTT00000067077 Transcript intron_variant - - - - - - rs531540 18:32635073 T ENSESTG00000020247 ENSESTT00000050914 Transcript intron_variant - - - - - - rs355303 18:33088632 T - - - intergenic_variant - - - - - - rs526370 18:34351405 A 80206 NM_025135.2 Transcript intron_variant - - - - - - rs526370 18:34351405 A CCDS32816.1 CCDS32816.1 Transcript intron_variant - - - - - - rs526370 18:34351405 A ENSESTG00000005292 ENSESTT00000013476 Transcript intron_variant - - - - - - rs2847590 18:34757320 A 57536 NM_020776.1 Transcript intron_variant - - - - - - rs2847590 18:34757320 A ENSESTG00000028125 ENSESTT00000070721 Transcript intron_variant - - - - - - rs2847590 18:34757320 A CCDS45855.1 CCDS45855.1 Transcript intron_variant - - - - - - rs6417077 18:35126317 C ENSESTG00000028327 ENSESTT00000071271 Transcript intron_variant - - - - - - rs6417077 18:35126317 C CCDS45856.1 CCDS45856.1 Transcript intron_variant - - - - - - rs6417077 18:35126317 C CCDS45857.1 CCDS45857.1 Transcript intron_variant - - - - - - rs6417077 18:35126317 C CCDS45858.1 CCDS45858.1 Transcript intron_variant - - - - - - rs6417077 18:35126317 C 56853 NM_001025089.1 Transcript intron_variant - - - - - - rs6417077 18:35126317 C 56853 NM_001025087.1 Transcript intron_variant - - - - - - rs6417077 18:35126317 C ENSESTG00000028327 ENSESTT00000071353 Transcript intron_variant - - - - - - rs6417077 18:35126317 C 56853 NM_001025088.1 Transcript intron_variant - - - - - - rs6417077 18:35126317 C CCDS32818.1 CCDS32818.1 Transcript intron_variant - - - - - - rs6417077 18:35126317 C 56853 NM_020180.3 Transcript intron_variant - - - - - - rs1187235 18:35346076 A - - - intergenic_variant - - - - - - rs959888 18:35675005 T - - - intergenic_variant - - - - - - rs1027994 18:35896214 A - - - intergenic_variant - - - - - - rs1196931 18:35901073 C - - - intergenic_variant - - - - - - rs6507254 18:36118066 G - - - intergenic_variant - - - - - - rs12965057 18:36146770 T - - - intergenic_variant - - - - - - rs8085566 18:36415713 C - - - intergenic_variant - - - - - - rs4324204 18:36441873 A - - - intergenic_variant - - - - - - rs6507306 18:36896671 G 647946 NR_024391.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6507306 18:36896671 G ENSESTG00000019845 ENSESTT00000049833 Transcript intron_variant - - - - - - rs6507306 18:36896671 G ENSESTG00000019939 ENSESTT00000049988 Transcript intron_variant - - - - - - rs6507306 18:36896671 G ENSESTG00000019845 ENSESTT00000049845 Transcript intron_variant - - - - - - rs8092331 18:36966513 C ENSESTG00000019845 ENSESTT00000049821 Transcript downstream_gene_variant - - - - - - DISTANCE=700 rs8092331 18:36966513 C 647946 NR_024391.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8092331 18:36966513 C ENSESTG00000019845 ENSESTT00000049833 Transcript intron_variant - - - - - - rs8092331 18:36966513 C ENSESTG00000019845 ENSESTT00000049845 Transcript intron_variant - - - - - - rs8092331 18:36966513 C ENSESTG00000019845 ENSESTT00000049880 Transcript intron_variant - - - - - - rs8092331 18:36966513 C ENSESTG00000019845 ENSESTT00000049866 Transcript intron_variant - - - - - - rs1368793 18:37907478 C - - - intergenic_variant - - - - - - rs7226451 18:37981907 G - - - intergenic_variant - - - - - - rs2602159 18:38574474 G - - - intergenic_variant - - - - - - rs4341831 18:38635925 A - - - intergenic_variant - - - - - - rs6507390 18:38637839 G - - - intergenic_variant - - - - - - rs6507398 18:38726084 T - - - intergenic_variant - - - - - - rs8090182 18:39185853 G - - - intergenic_variant - - - - - - rs1432149 18:39391222 T ENSESTG00000015270 ENSESTT00000038250 Transcript intron_variant - - - - - - rs8088216 18:39431088 T - - - intergenic_variant - - - - - - rs3133075 18:39568808 A 5289 NM_002647.2 Transcript intron_variant - - - - - - rs3133075 18:39568808 A ENSESTG00000025883 ENSESTT00000065633 Transcript intron_variant - - - - - - rs3133075 18:39568808 A ENSESTG00000025883 ENSESTT00000065648 Transcript intron_variant - - - - - - rs3133075 18:39568808 A ENSESTG00000025883 ENSESTT00000065611 Transcript intron_variant - - - - - - rs3133075 18:39568808 A ENSESTG00000025883 ENSESTT00000065618 Transcript intron_variant - - - - - - rs3133075 18:39568808 A CCDS11920.1 CCDS11920.1 Transcript intron_variant - - - - - - rs3133075 18:39568808 A ENSESTG00000025883 ENSESTT00000065254 Transcript intron_variant - - - - - - rs3133200 18:39568812 C 5289 NM_002647.2 Transcript intron_variant - - - - - - rs3133200 18:39568812 C ENSESTG00000025883 ENSESTT00000065633 Transcript intron_variant - - - - - - rs3133200 18:39568812 C ENSESTG00000025883 ENSESTT00000065648 Transcript intron_variant - - - - - - rs3133200 18:39568812 C ENSESTG00000025883 ENSESTT00000065611 Transcript intron_variant - - - - - - rs3133200 18:39568812 C ENSESTG00000025883 ENSESTT00000065618 Transcript intron_variant - - - - - - rs3133200 18:39568812 C CCDS11920.1 CCDS11920.1 Transcript intron_variant - - - - - - rs3133200 18:39568812 C ENSESTG00000025883 ENSESTT00000065254 Transcript intron_variant - - - - - - rs346176 18:40001563 T 284260 NR_046455.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs346176 18:40001563 T 284260 NR_046454.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs346176 18:40001563 T ENSESTG00000026136 ENSESTT00000065867 Transcript intron_variant - - - - - - rs346176 18:40001563 T 284260 NR_046174.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs346176 18:40001563 T 284260 NR_046456.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs346176 18:40001563 T 284260 NR_046457.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4603651 18:40174407 G 284260 NR_046174.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs8095496 18:40186042 C 284260 NR_046174.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs8090159 18:40653613 C ENSESTG00000026157 ENSESTT00000066128 Transcript intron_variant - - - - - - rs8090159 18:40653613 C ENSESTG00000026157 ENSESTT00000066163 Transcript intron_variant - - - - - - rs8090159 18:40653613 C 6014 NM_002930.2 Transcript intron_variant - - - - - - rs8090159 18:40653613 C ENSESTG00000026157 ENSESTT00000066116 Transcript intron_variant - - - - - - rs8090159 18:40653613 C CCDS11921.1 CCDS11921.1 Transcript intron_variant - - - - - - rs2056230 18:40701836 T - - - intergenic_variant - - - - - - rs816756 18:40785522 C - - - intergenic_variant - - - - - - rs816754 18:40802563 G - - - intergenic_variant - - - - - - rs2572268 18:41052777 C - - - intergenic_variant - - - - - - rs2622799 18:41055087 A - - - intergenic_variant - - - - - - rs2204615 18:41155097 C - - - intergenic_variant - - - - - - rs9304292 18:41179374 T - - - intergenic_variant - - - - - - rs4569365 18:41195461 T - - - intergenic_variant - - - - - - rs994497 18:41215778 G - - - intergenic_variant - - - - - - rs2204616 18:41234129 T - - - intergenic_variant - - - - - - rs7237582 18:41277273 G - - - intergenic_variant - - - - - - rs7232831 18:41334123 C - - - intergenic_variant - - - - - - rs8096412 18:41353555 C - - - intergenic_variant - - - - - - rs640197 18:41809081 G ENSESTG00000007730 ENSESTT00000019480 Transcript intron_variant - - - - - - rs4293454 18:41917068 A ENSESTG00000007724 ENSESTT00000019461 Transcript intron_variant - - - - - - rs1511753 18:42138917 C - - - intergenic_variant - - - - - - rs10853526 18:42445940 C CCDS11923.2 CCDS11923.2 Transcript intron_variant - - - - - - rs10853526 18:42445940 C ENSESTG00000007714 ENSESTT00000019434 Transcript intron_variant - - - - - - rs10853526 18:42445940 C CCDS45859.1 CCDS45859.1 Transcript intron_variant - - - - - - rs10853526 18:42445940 C 26040 NM_015559.2 Transcript intron_variant - - - - - - rs10853526 18:42445940 C ENSESTG00000007714 ENSESTT00000019441 Transcript intron_variant - - - - - - rs10853526 18:42445940 C 26040 NM_001130110.1 Transcript intron_variant - - - - - - rs678683 18:42446822 G CCDS11923.2 CCDS11923.2 Transcript intron_variant - - - - - - rs678683 18:42446822 G ENSESTG00000007714 ENSESTT00000019434 Transcript intron_variant - - - - - - rs678683 18:42446822 G CCDS45859.1 CCDS45859.1 Transcript intron_variant - - - - - - rs678683 18:42446822 G 26040 NM_015559.2 Transcript intron_variant - - - - - - rs678683 18:42446822 G ENSESTG00000007714 ENSESTT00000019441 Transcript intron_variant - - - - - - rs678683 18:42446822 G 26040 NM_001130110.1 Transcript intron_variant - - - - - - rs4287662 18:42519344 G - ENSR00000525186 RegulatoryFeature regulatory_region_variant - - - - - - rs4287662 18:42519344 G CCDS11923.2 CCDS11923.2 Transcript intron_variant - - - - - - rs4287662 18:42519344 G ENSESTG00000007714 ENSESTT00000019434 Transcript intron_variant - - - - - - rs4287662 18:42519344 G 26040 NM_015559.2 Transcript intron_variant - - - - - - rs4287662 18:42519344 G ENSESTG00000007714 ENSESTT00000019441 Transcript intron_variant - - - - - - rs4890505 18:42619200 G CCDS11923.2 CCDS11923.2 Transcript intron_variant - - - - - - rs4890505 18:42619200 G 26040 NM_015559.2 Transcript intron_variant - - - - - - rs4890505 18:42619200 G ENSESTG00000016141 ENSESTT00000040510 Transcript intron_variant - - - - - - rs6507593 18:42651201 T 26040 NM_015559.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2726 rs1551823 18:42904320 C - ENSR00001514740 RegulatoryFeature regulatory_region_variant - - - - - - rs1551823 18:42904320 C 8170 NM_001242692.1 Transcript intron_variant - - - - - - rs2612564 18:42987891 A 8170 NM_001242692.1 Transcript intron_variant - - - - - - rs2612568 18:43000628 A ENSESTG00000016297 ENSESTT00000040884 Transcript downstream_gene_variant - - - - - - DISTANCE=3102 rs2612568 18:43000628 A 8170 NM_001242692.1 Transcript intron_variant - - - - - - rs2612568 18:43000628 A ENSESTG00000016297 ENSESTT00000040890 Transcript downstream_gene_variant - - - - - - DISTANCE=3105 rs2542972 18:43014007 C ENSESTG00000016297 ENSESTT00000040884 Transcript intron_variant - - - - - - rs2542972 18:43014007 C ENSESTG00000016294 ENSESTT00000040876 Transcript downstream_gene_variant - - - - - - DISTANCE=4144 rs2542972 18:43014007 C 8170 NM_001242692.1 Transcript intron_variant - - - - - - rs2542972 18:43014007 C ENSESTG00000016297 ENSESTT00000040890 Transcript intron_variant - - - - - - rs2852278 18:43120417 G ENSESTG00000016153 ENSESTT00000040532 Transcript intron_variant - - - - - - rs2852278 18:43120417 G 8170 NM_001242692.1 Transcript intron_variant - - - - - - rs8090867 18:43249943 C 8170 NM_007163.3 Transcript intron_variant - - - - - - rs8090867 18:43249943 C CCDS11924.1 CCDS11924.1 Transcript intron_variant - - - - - - rs8090867 18:43249943 C 8170 NM_001242692.1 Transcript intron_variant - - - - - - rs900974 18:43303982 G CCDS45860.1 CCDS45860.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3255 rs900974 18:43303982 G 6563 NM_001146036.2 Transcript upstream_gene_variant - - - - - - DISTANCE=110 rs900974 18:43303982 G 6563 NM_015865.6 Transcript upstream_gene_variant - - - - - - DISTANCE=110 rs900974 18:43303982 G ENSESTG00000016174 ENSESTT00000040619 Transcript upstream_gene_variant - - - - - - DISTANCE=133 rs900974 18:43303982 G 6563 NM_001146037.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2936 rs900974 18:43303982 G ENSESTG00000016174 ENSESTT00000040609 Transcript upstream_gene_variant - - - - - - DISTANCE=110 rs900974 18:43303982 G 6563 NM_001128588.3 Transcript upstream_gene_variant - - - - - - DISTANCE=110 rs900974 18:43303982 G ENSESTG00000016174 ENSESTT00000040628 Transcript upstream_gene_variant - - - - - - DISTANCE=134 rs900974 18:43303982 G ENSESTG00000016174 ENSESTT00000040633 Transcript upstream_gene_variant - - - - - - DISTANCE=874 rs900974 18:43303982 G ENSESTG00000016174 ENSESTT00000040644 Transcript upstream_gene_variant - - - - - - DISTANCE=2708 rs900974 18:43303982 G ENSESTG00000016166 ENSESTT00000040555 Transcript downstream_gene_variant - - - - - - DISTANCE=241 rs2918085 18:43583588 C CCDS32820.2 CCDS32820.2 Transcript intron_variant - - - - - - rs2918085 18:43583588 C 9050 NM_024430.3 Transcript intron_variant - - - - - - rs2918085 18:43583588 C ENSESTG00000016264 ENSESTT00000040924 Transcript intron_variant - - - - - - rs2918085 18:43583588 C ENSESTG00000016264 ENSESTT00000040912 Transcript intron_variant - - - - - - rs2918085 18:43583588 C ENSESTG00000016264 ENSESTT00000040934 Transcript intron_variant - - - - - - rs473371 18:43610235 C CCDS32820.2 CCDS32820.2 Transcript intron_variant - - - - - - rs473371 18:43610235 C 9050 NM_024430.3 Transcript intron_variant - - - - - - rs473371 18:43610235 C ENSESTG00000016264 ENSESTT00000040924 Transcript intron_variant - - - - - - rs473371 18:43610235 C ENSESTG00000016264 ENSESTT00000040912 Transcript intron_variant - - - - - - rs586113 18:43611300 A CCDS32820.2 CCDS32820.2 Transcript intron_variant - - - - - - rs586113 18:43611300 A 9050 NM_024430.3 Transcript intron_variant - - - - - - rs586113 18:43611300 A ENSESTG00000016264 ENSESTT00000040924 Transcript intron_variant - - - - - - rs586113 18:43611300 A ENSESTG00000016264 ENSESTT00000040912 Transcript intron_variant - - - - - - rs1791416 18:43631645 A CCDS32820.2 CCDS32820.2 Transcript intron_variant - - - - - - rs1791416 18:43631645 A 9050 NM_024430.3 Transcript intron_variant - - - - - - rs1791416 18:43631645 A ENSESTG00000016264 ENSESTT00000040912 Transcript intron_variant - - - - - - rs6507683 18:43769286 C 147339 NM_145055.3 Transcript intron_variant - - - - - - rs6507683 18:43769286 C ENSESTG00000015931 ENSESTT00000039938 Transcript intron_variant - - - - - - rs6507683 18:43769286 C ENSESTG00000015931 ENSESTT00000039934 Transcript intron_variant - - - - - - rs6507683 18:43769286 C 147339 NM_001008239.2 Transcript intron_variant - - - - - - rs6507683 18:43769286 C ENSESTG00000015931 ENSESTT00000039950 Transcript intron_variant - - - - - - rs9956233 18:43843736 G 147339 NM_145055.3 Transcript 3_prime_UTR_variant 2246 - - - - - rs9956233 18:43843736 G CCDS42431.1 CCDS42431.1 Transcript downstream_gene_variant - - - - - - DISTANCE=655 rs9956233 18:43843736 G CCDS42430.1 CCDS42430.1 Transcript downstream_gene_variant - - - - - - DISTANCE=655 rs9956233 18:43843736 G 147339 NM_001008239.2 Transcript 3_prime_UTR_variant 2063 - - - - - rs7240808 18:43985821 T ENSESTG00000015844 ENSESTT00000039771 Transcript intron_variant - - - - - - rs7240808 18:43985821 T 494470 NM_001256758.1 Transcript intron_variant - - - - - - rs7240808 18:43985821 T ENSESTG00000015844 ENSESTT00000039730 Transcript intron_variant - - - - - - rs7240808 18:43985821 T CCDS32823.1 CCDS32823.1 Transcript intron_variant - - - - - - rs7240808 18:43985821 T 494470 NM_152470.2 Transcript intron_variant - - - - - - rs7240808 18:43985821 T ENSESTG00000015844 ENSESTT00000039756 Transcript intron_variant - - - - - - rs7240808 18:43985821 T ENSESTG00000015844 ENSESTT00000039764 Transcript intron_variant - - - - - - rs328148 18:44170653 T 125336 NM_144612.6 Transcript intron_variant - - - - - - rs2943796 18:44240084 G ENSESTG00000016112 ENSESTT00000040404 Transcript upstream_gene_variant - - - - - - DISTANCE=3147 rs2943796 18:44240084 G 125336 NM_144612.6 Transcript upstream_gene_variant - - - - - - DISTANCE=3088 rs7235968 18:44329319 G CCDS11930.1 CCDS11930.1 Transcript intron_variant - - - - - - rs7235968 18:44329319 G ENSESTG00000016099 ENSESTT00000040364 Transcript intron_variant - - - - - - rs7235968 18:44329319 G ENSESTG00000016099 ENSESTT00000040376 Transcript intron_variant - - - - - - rs7235968 18:44329319 G 29906 NM_013305.4 Transcript intron_variant - - - - - - rs7235968 18:44329319 G ENSESTG00000016099 ENSESTT00000040370 Transcript intron_variant - - - - - - rs7235968 18:44329319 G ENSESTG00000016028 ENSESTT00000040185 Transcript intron_variant - - - - - - rs7235968 18:44329319 G ENSESTG00000016099 ENSESTT00000040385 Transcript intron_variant - - - - - - rs6417096 18:44353344 C - - - intergenic_variant - - - - - - rs2187093 18:44529048 G ENSESTG00000007614 ENSESTT00000019184 Transcript intron_variant - - - - - - rs2187093 18:44529048 G ENSESTG00000007614 ENSESTT00000019175 Transcript intron_variant - - - - - - rs2187093 18:44529048 G 83473 NM_031303.2 Transcript intron_variant - - - - - - rs2187093 18:44529048 G ENSESTG00000007614 ENSESTT00000019198 Transcript downstream_gene_variant - - - - - - DISTANCE=2787 rs2187093 18:44529048 G ENSESTG00000007614 ENSESTT00000019209 Transcript intron_variant - - - - - - rs2187093 18:44529048 G ENSESTG00000007614 ENSESTT00000019194 Transcript intron_variant - - - - - - rs2187093 18:44529048 G ENSESTG00000007614 ENSESTT00000019212 Transcript intron_variant - - - - - - rs7240173 18:45055808 A ENSESTG00000007642 ENSESTT00000019250 Transcript intron_variant - - - - - - rs7240173 18:45055808 A ENSESTG00000007637 ENSESTT00000019240 Transcript intron_variant - - - - - - rs4468698 18:45106105 G ENSESTG00000007637 ENSESTT00000019240 Transcript intron_variant - - - - - - rs2316517 18:45202957 G ENSESTG00000007649 ENSESTT00000019260 Transcript intron_variant - - - - - - rs2852962 18:45262082 T - - - intergenic_variant - - - - - - rs905312 18:45328107 C - - - intergenic_variant - - - - - - rs1792661 18:45349395 T - - - intergenic_variant - - - - - - rs1787179 18:45352520 G - - - intergenic_variant - - - - - - rs1787187 18:45367484 G 4087 NM_005901.5 Transcript 3_prime_UTR_variant 2410 - - - - - rs1787187 18:45367484 G ENSESTG00000007652 ENSESTT00000019287 Transcript downstream_gene_variant - - - - - - DISTANCE=596 rs1787187 18:45367484 G CCDS11934.1 CCDS11934.1 Transcript downstream_gene_variant - - - - - - DISTANCE=714 rs1787187 18:45367484 G 4087 NM_001135937.2 Transcript 3_prime_UTR_variant 2428 - - - - - rs1787187 18:45367484 G 4087 NM_001003652.3 Transcript 3_prime_UTR_variant 2518 - - - - - rs6507840 18:45837779 C ENSESTG00000032043 ENSESTT00000080858 Transcript intron_variant - - - - - - rs6507840 18:45837779 C ENSESTG00000032054 ENSESTT00000080883 Transcript downstream_gene_variant - - - - - - DISTANCE=3150 rs4940369 18:45927814 C - - - intergenic_variant - - - - - - rs1384228 18:46270191 A ENSESTG00000031865 ENSESTT00000080533 Transcript intron_variant - - - - - - rs1384228 18:46270191 A 9811 NM_001142397.1 Transcript intron_variant - - - - - - rs1384228 18:46270191 A 9811 NM_014772.2 Transcript intron_variant - - - - - - rs1384228 18:46270191 A CCDS45864.1 CCDS45864.1 Transcript intron_variant - - - - - - rs1384228 18:46270191 A ENSESTG00000031865 ENSESTT00000080487 Transcript intron_variant - - - - - - rs1384228 18:46270191 A ENSESTG00000031865 ENSESTT00000080516 Transcript intron_variant - - - - - - rs1384228 18:46270191 A CCDS11935.1 CCDS11935.1 Transcript intron_variant - - - - - - rs1384228 18:46270191 A ENSESTG00000031865 ENSESTT00000080508 Transcript intron_variant - - - - - - rs1384228 18:46270191 A ENSESTG00000031865 ENSESTT00000080542 Transcript intron_variant - - - - - - rs4363913 18:46339048 C 9811 NM_014772.2 Transcript intron_variant - - - - - - rs4363913 18:46339048 C CCDS45864.1 CCDS45864.1 Transcript intron_variant - - - - - - rs4363913 18:46339048 C CCDS11935.1 CCDS11935.1 Transcript intron_variant - - - - - - rs4363913 18:46339048 C 9811 NM_001142397.1 Transcript intron_variant - - - - - - rs502089 18:46809655 T ENSESTG00000000305 ENSESTT00000000795 Transcript intron_variant - - - - - - rs502089 18:46809655 T ENSESTG00000000305 ENSESTT00000000789 Transcript intron_variant - - - - - - rs502089 18:46809655 T ENSESTG00000000305 ENSESTT00000000788 Transcript intron_variant - - - - - - rs502089 18:46809655 T ENSESTG00000000305 ENSESTT00000000776 Transcript intron_variant - - - - - - rs502089 18:46809655 T 54808 NM_017653.3 Transcript intron_variant - - - - - - rs502089 18:46809655 T ENSESTG00000000305 ENSESTT00000000786 Transcript intron_variant - - - - - - rs502089 18:46809655 T CCDS11937.1 CCDS11937.1 Transcript intron_variant - - - - - - rs502089 18:46809655 T ENSESTG00000000305 ENSESTT00000000791 Transcript downstream_gene_variant - - - - - - DISTANCE=3168 rs10432200 18:47073555 C - - - intergenic_variant - - - - - - rs948645 18:47400654 C - ENSR00000668116 RegulatoryFeature regulatory_region_variant - - - - - - rs948645 18:47400654 C ENSESTG00000000241 ENSESTT00000000626 Transcript intron_variant - - - - - - rs948645 18:47400654 C ENSESTG00000000241 ENSESTT00000000635 Transcript downstream_gene_variant - - - - - - DISTANCE=3472 rs948645 18:47400654 C ENSESTG00000000241 ENSESTT00000000629 Transcript downstream_gene_variant - - - - - - DISTANCE=3472 rs948645 18:47400654 C ENSESTG00000000241 ENSESTT00000000637 Transcript intron_variant - - - - - - rs948645 18:47400654 C ENSESTG00000000241 ENSESTT00000000628 Transcript intron_variant - - - - - - rs948645 18:47400654 C 4645 NM_001080467.2 Transcript intron_variant - - - - - - rs948645 18:47400654 C CCDS42436.1 CCDS42436.1 Transcript intron_variant - - - - - - rs948645 18:47400654 C ENSESTG00000000241 ENSESTT00000000633 Transcript intron_variant - - - - - - rs948645 18:47400654 C ENSESTG00000000241 ENSESTT00000000634 Transcript intron_variant - - - - - - rs3132919 18:47427377 C ENSESTG00000000241 ENSESTT00000000626 Transcript intron_variant - - - - - - rs3132919 18:47427377 C ENSESTG00000000241 ENSESTT00000000635 Transcript intron_variant - - - - - - rs3132919 18:47427377 C ENSESTG00000000241 ENSESTT00000000629 Transcript intron_variant - - - - - - rs3132919 18:47427377 C ENSESTG00000000241 ENSESTT00000000628 Transcript intron_variant - - - - - - rs3132919 18:47427377 C 4645 NM_001080467.2 Transcript intron_variant - - - - - - rs3132919 18:47427377 C CCDS42436.1 CCDS42436.1 Transcript intron_variant - - - - - - rs3132919 18:47427377 C ENSESTG00000000241 ENSESTT00000000633 Transcript intron_variant - - - - - - rs3132919 18:47427377 C ENSESTG00000000241 ENSESTT00000000634 Transcript intron_variant - - - - - - rs6507958 18:47495876 T CCDS42436.1 CCDS42436.1 Transcript intron_variant - - - - - - rs6507958 18:47495876 T ENSESTG00000000635 ENSESTT00000001539 Transcript intron_variant - - - - - - rs6507958 18:47495876 T 4645 NM_001080467.2 Transcript intron_variant - - - - - - rs2666930 18:47574906 T ENSESTG00000000633 ENSESTT00000001509 Transcript intron_variant - - - - - - rs2666930 18:47574906 T ENSESTG00000000633 ENSESTT00000001505 Transcript intron_variant - - - - - - rs2666930 18:47574906 T CCDS42436.1 CCDS42436.1 Transcript intron_variant - - - - - - rs2666930 18:47574906 T 4645 NM_001080467.2 Transcript intron_variant - - - - - - rs11082801 18:47603251 C ENSESTG00000000633 ENSESTT00000001509 Transcript intron_variant - - - - - - rs11082801 18:47603251 C ENSESTG00000000633 ENSESTT00000001505 Transcript intron_variant - - - - - - rs11082801 18:47603251 C CCDS42436.1 CCDS42436.1 Transcript intron_variant - - - - - - rs11082801 18:47603251 C 4645 NM_001080467.2 Transcript intron_variant - - - - - - rs8085101 18:47616374 C ENSESTG00000000633 ENSESTT00000001509 Transcript intron_variant - - - - - - rs8085101 18:47616374 C ENSESTG00000000633 ENSESTT00000001505 Transcript intron_variant - - - - - - rs8085101 18:47616374 C CCDS42436.1 CCDS42436.1 Transcript intron_variant - - - - - - rs8085101 18:47616374 C ENSESTG00000000579 ENSESTT00000001384 Transcript downstream_gene_variant - - - - - - DISTANCE=2433 rs8085101 18:47616374 C 4645 NM_001080467.2 Transcript intron_variant - - - - - - rs7506978 18:47633822 C ENSESTG00000000633 ENSESTT00000001505 Transcript intron_variant - - - - - - rs7506978 18:47633822 C CCDS42436.1 CCDS42436.1 Transcript intron_variant - - - - - - rs7506978 18:47633822 C ENSESTG00000000529 ENSESTT00000001278 Transcript intron_variant - - - - - - rs7506978 18:47633822 C ENSESTG00000000579 ENSESTT00000001384 Transcript intron_variant - - - - - - rs7506978 18:47633822 C 4645 NM_001080467.2 Transcript intron_variant - - - - - - rs3017279 18:47958922 A - - - intergenic_variant - - - - - - rs2849238 18:48346497 G - ENSR00001515195 RegulatoryFeature regulatory_region_variant - - - - - - rs2849238 18:48346497 G CCDS45867.1 CCDS45867.1 Transcript upstream_gene_variant - - - - - - DISTANCE=212 rs2849238 18:48346497 G CCDS45868.1 CCDS45868.1 Transcript upstream_gene_variant - - - - - - DISTANCE=212 rs2849238 18:48346497 G ENSESTG00000000571 ENSESTT00000001365 Transcript intron_variant - - - - - - rs2849238 18:48346497 G 83876 NM_001127175.1 Transcript upstream_gene_variant - - - - - - DISTANCE=63 rs2849238 18:48346497 G ENSESTG00000000571 ENSESTT00000001369 Transcript upstream_gene_variant - - - - - - DISTANCE=291 rs2849238 18:48346497 G 83876 NM_001127174.1 Transcript intron_variant - - - - - - rs2849238 18:48346497 G 83876 NM_001127176.1 Transcript upstream_gene_variant - - - - - - DISTANCE=63 rs2849238 18:48346497 G 83876 NM_031939.3 Transcript upstream_gene_variant - - - - - - DISTANCE=63 rs2849238 18:48346497 G ENSESTG00000000571 ENSESTT00000001368 Transcript upstream_gene_variant - - - - - - DISTANCE=126 rs2847572 18:48373126 G - - - intergenic_variant - - - - - - rs2848802 18:48629199 A - - - intergenic_variant - - - - - - rs7230090 18:48665335 C - - - intergenic_variant - - - - - - rs4245235 18:48668931 T - - - intergenic_variant - - - - - - rs8086510 18:48704723 A ENSESTG00000008504 ENSESTT00000021414 Transcript intron_variant - - - - - - rs8086510 18:48704723 A CCDS11951.2 CCDS11951.2 Transcript intron_variant - - - - - - rs8086510 18:48704723 A 51320 NM_016626.4 Transcript intron_variant - - - - - - rs6508051 18:48734588 C - - - intergenic_variant - - - - - - rs9653023 18:48758957 G - - - intergenic_variant - - - - - - rs9957548 18:48765690 C - - - intergenic_variant - - - - - - rs8096574 18:48773196 C - - - intergenic_variant - - - - - - rs4633813 18:48785748 A - - - intergenic_variant - - - - - - rs6508056 18:48791305 G - - - intergenic_variant - - - - - - rs7235045 18:48793248 G - ENSR00001515230 RegulatoryFeature regulatory_region_variant - - - - - - rs7235045 18:48793248 G - - - intergenic_variant - - - - - - rs9960878 18:48824451 C - - - intergenic_variant - - - - - - rs2445452 18:48838878 G - - - intergenic_variant - - - - - - rs2442960 18:48843328 C - - - intergenic_variant - - - - - - rs2923064 18:48847801 T - - - intergenic_variant - - - - - - rs1947505 18:48869863 T - - - intergenic_variant - - - - - - rs2442949 18:48874616 G - - - intergenic_variant - - - - - - rs2445463 18:48880731 G - - - intergenic_variant - - - - - - rs1902333 18:48880926 C - - - intergenic_variant - - - - - - rs1466271 18:48881924 G - - - intergenic_variant - - - - - - rs2442967 18:48883960 T - - - intergenic_variant - - - - - - rs1672232 18:48888442 A - - - intergenic_variant - - - - - - rs2442970 18:48903298 G - - - intergenic_variant - - - - - - rs1656757 18:48938544 G 100287225 NR_040074.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1656757 18:48938544 G ENSESTG00000008499 ENSESTT00000021396 Transcript intron_variant - - - - - - rs1656757 18:48938544 G 100287225 NR_040075.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1625142 18:48989743 T 100287225 NR_040074.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1625142 18:48989743 T ENSESTG00000008499 ENSESTT00000021396 Transcript intron_variant - - - - - - rs1625142 18:48989743 T 100287225 NR_040075.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs321838 18:48996009 T 100287225 NR_040074.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs321838 18:48996009 T ENSESTG00000008499 ENSESTT00000021396 Transcript downstream_gene_variant - - - - - - DISTANCE=3898 rs321838 18:48996009 T 100287225 NR_040075.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1261 rs186512 18:48998940 A 100287225 NR_040074.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs186512 18:48998940 A 100287225 NR_040075.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4192 rs1786872 18:49027108 G 100287225 NR_040074.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1947875 18:49394130 C - ENSR00000668143 RegulatoryFeature regulatory_region_variant - - - - - - rs1947875 18:49394130 C - - - intergenic_variant - - - - - - rs2928936 18:49440073 T - - - intergenic_variant - - - - - - rs2928938 18:49441491 T - - - intergenic_variant - - - - - - rs76219304 18:49515453 C - - - intergenic_variant - - - - - - rs352136 18:49832535 G ENSESTG00000035248 ENSESTT00000089030 Transcript downstream_gene_variant - - - - - - DISTANCE=2387 rs1228471 18:49997540 G 1630 NM_005215.3 Transcript intron_variant - - - - - - rs1228471 18:49997540 G CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs1228471 18:49997540 G ENSESTG00000035248 ENSESTT00000089030 Transcript intron_variant - - - - - - rs1145251 18:50010917 G 1630 NM_005215.3 Transcript intron_variant - - - - - - rs1145251 18:50010917 G CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs1145251 18:50010917 G ENSESTG00000035248 ENSESTT00000089030 Transcript upstream_gene_variant - - - - - - DISTANCE=4322 rs1145254 18:50015126 G 1630 NM_005215.3 Transcript intron_variant - - - - - - rs1145254 18:50015126 G CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs982984 18:50031427 A 1630 NM_005215.3 Transcript intron_variant - - - - - - rs982984 18:50031427 A CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs1144073 18:50065957 T 1630 NM_005215.3 Transcript intron_variant - - - - - - rs1144073 18:50065957 T CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs1145276 18:50069973 G 1630 NM_005215.3 Transcript intron_variant - - - - - - rs1145276 18:50069973 G CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs11082941 18:50226883 G 1630 NM_005215.3 Transcript intron_variant - - - - - - rs11082941 18:50226883 G CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs4940215 18:50326950 C ENSESTG00000035241 ENSESTT00000089021 Transcript intron_variant - - - - - - rs4940215 18:50326950 C ENSESTG00000035241 ENSESTT00000089015 Transcript intron_variant - - - - - - rs4940215 18:50326950 C 1630 NM_005215.3 Transcript intron_variant - - - - - - rs4940215 18:50326950 C ENSESTG00000035241 ENSESTT00000089018 Transcript intron_variant - - - - - - rs4940215 18:50326950 C CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs6508185 18:50547530 G 1630 NM_005215.3 Transcript intron_variant - - - - - - rs6508185 18:50547530 G CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs6508185 18:50547530 G ENSESTG00000009317 ENSESTT00000023348 Transcript intron_variant - - - - - - rs4603635 18:50670481 T ENSESTG00000009325 ENSESTT00000023369 Transcript intron_variant - - - - - - rs4603635 18:50670481 T 1630 NM_005215.3 Transcript intron_variant - - - - - - rs4603635 18:50670481 T CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs4497763 18:50731829 G ENSESTG00000009325 ENSESTT00000023369 Transcript intron_variant - - - - - - rs4497763 18:50731829 G 1630 NM_005215.3 Transcript intron_variant - - - - - - rs4497763 18:50731829 G CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs9945787 18:50883371 G 1630 NM_005215.3 Transcript intron_variant - - - - - - rs9945787 18:50883371 G CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs4625792 18:51017277 C ENSESTG00000009343 ENSESTT00000023420 Transcript intron_variant - - - - - - rs4625792 18:51017277 C 1630 NM_005215.3 Transcript intron_variant - - - - - - rs4625792 18:51017277 C CCDS11952.1 CCDS11952.1 Transcript intron_variant - - - - - - rs9959713 18:51172778 A - - - intergenic_variant - - - - - - rs2958093 18:51572755 G - - - intergenic_variant - - - - - - rs662939 18:51775417 A - - - intergenic_variant - - - - - - rs9949993 18:52673774 C - - - intergenic_variant - - - - - - rs7233235 18:52694163 G - - - intergenic_variant - - - - - - rs7234835 18:52703618 C - - - intergenic_variant - - - - - - rs4801130 18:52709329 A - - - intergenic_variant - - - - - - rs1238847 18:53287495 C CCDS58631.1 CCDS58631.1 Transcript intron_variant - - - - - - rs1238847 18:53287495 C 6925 NM_001243226.1 Transcript intron_variant - - - - - - rs610032 18:53307272 G CCDS58631.1 CCDS58631.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4144 rs610032 18:53307272 G 6925 NM_001243226.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4084 rs589201 18:53317477 T - - - intergenic_variant - - - - - - rs619354 18:53326176 G - - - intergenic_variant - - - - - - rs1615008 18:53327528 G - - - intergenic_variant - - - - - - rs616375 18:53330670 C - - - intergenic_variant - - - - - - rs784327 18:53478695 C - - - intergenic_variant - - - - - - rs1848073 18:53584457 C - - - intergenic_variant - - - - - - rs1792706 18:53771696 A 100505474 NR_040026.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1792706 18:53771696 A 100505474 NR_040025.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs725498 18:53780734 A 100505474 NR_040026.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs725498 18:53780734 A 100505474 NR_040025.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1235375 18:53873181 T - - - intergenic_variant - - - - - - rs9319891 18:54161952 G - - - intergenic_variant - - - - - - rs636363 18:54201634 C - - - intergenic_variant - - - - - - rs578973 18:54243303 C - ENSR00001515526 RegulatoryFeature regulatory_region_variant - - - - - - rs578973 18:54243303 C - - - intergenic_variant - - - - - - rs655522 18:54296321 G ENSESTG00000012879 ENSESTT00000032305 Transcript intron_variant - - - - - - rs655522 18:54296321 G 9352 NM_004786.2 Transcript intron_variant - - - - - - rs655522 18:54296321 G ENSESTG00000012879 ENSESTT00000032294 Transcript intron_variant - - - - - - rs655522 18:54296321 G CCDS11961.1 CCDS11961.1 Transcript intron_variant - - - - - - rs655522 18:54296321 G 9352 NR_024546.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs664455 18:54310908 T 9352 NM_004786.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4988 rs664455 18:54310908 T ENSESTG00000012879 ENSESTT00000032294 Transcript intron_variant - - - - - - rs664455 18:54310908 T 9352 NR_024546.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4988 rs1787459 18:54630020 C ENSESTG00000031304 ENSESTT00000078953 Transcript intron_variant - - - - - - rs1787459 18:54630020 C 23335 NM_052834.2 Transcript intron_variant - - - - - - rs1787459 18:54630020 C CCDS11963.1 CCDS11963.1 Transcript intron_variant - - - - - - rs1787459 18:54630020 C 23335 NM_015285.2 Transcript intron_variant - - - - - - rs1787459 18:54630020 C CCDS11962.1 CCDS11962.1 Transcript intron_variant - - - - - - rs8092187 18:54904171 G - - - intergenic_variant - - - - - - rs9945973 18:54955885 T - - - intergenic_variant - - - - - - rs474264 18:55234501 A ENSESTG00000031572 ENSESTT00000079779 Transcript intron_variant - - - - - - rs474264 18:55234501 A ENSESTG00000031572 ENSESTT00000079731 Transcript intron_variant - - - - - - rs474264 18:55234501 A CCDS11964.1 CCDS11964.1 Transcript intron_variant - - - - - - rs474264 18:55234501 A ENSESTG00000031572 ENSESTT00000079763 Transcript intron_variant - - - - - - rs474264 18:55234501 A ENSESTG00000031572 ENSESTT00000079742 Transcript downstream_gene_variant - - - - - - DISTANCE=576 rs474264 18:55234501 A 2235 NM_001012515.2 Transcript intron_variant - - - - - - rs474264 18:55234501 A 2235 NM_000140.3 Transcript intron_variant - - - - - - rs474264 18:55234501 A CCDS32836.1 CCDS32836.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A - ENSR00000526672 RegulatoryFeature regulatory_region_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079070 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078856 Transcript intron_variant - - - - - - rs292454 18:55888439 A CCDS45873.1 CCDS45873.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A 23327 NM_015277.5 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078904 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078799 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078606 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078332 Transcript intron_variant - - - - - - rs292454 18:55888439 A 23327 NM_001144971.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078485 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078384 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079189 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079128 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078490 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078921 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079120 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A CCDS45872.1 CCDS45872.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A 23327 NM_001144968.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078814 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078702 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078281 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078680 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078912 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078986 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078420 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079157 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078510 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078650 Transcript intron_variant - - - - - - rs292454 18:55888439 A 23327 NM_001144964.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078504 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078807 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078675 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078618 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078803 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078816 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079179 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078667 Transcript intron_variant - - - - - - rs292454 18:55888439 A 23327 NM_001144970.2 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079014 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078659 Transcript intron_variant - - - - - - rs292454 18:55888439 A 23327 NM_001144966.2 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079168 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079199 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079160 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079027 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078824 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078443 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078955 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079147 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078925 Transcript intron_variant - - - - - - rs292454 18:55888439 A 23327 NM_001144969.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078302 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078350 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079049 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078737 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079137 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A 23327 NM_001243960.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078239 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078682 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079060 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078946 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079077 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078480 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078292 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078779 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078552 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078760 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078787 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078456 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079041 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078253 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078271 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079091 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078865 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078216 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078686 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078434 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078472 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079184 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079023 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079164 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078225 Transcript intron_variant - - - - - - rs292454 18:55888439 A CCDS58632.1 CCDS58632.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078561 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079001 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078833 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078768 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078640 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078776 Transcript intron_variant - - - - - - rs292454 18:55888439 A CCDS45874.1 CCDS45874.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078888 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078593 Transcript intron_variant - - - - - - rs292454 18:55888439 A 23327 NM_001144965.1 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078750 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078534 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079202 Transcript upstream_gene_variant - - - - - - DISTANCE=364 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079034 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A 23327 NM_001144967.2 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078268 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078235 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079086 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078464 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078583 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078797 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078935 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078318 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000078393 Transcript intron_variant - - - - - - rs292454 18:55888439 A ENSESTG00000030971 ENSESTT00000079107 Transcript upstream_gene_variant - - - - - - DISTANCE=315 rs3865417 18:55989221 A - ENSR00000526704 RegulatoryFeature regulatory_region_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079399 Transcript intron_variant - - - - - - rs3865417 18:55989221 A CCDS45873.1 CCDS45873.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079270 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079217 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079360 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078799 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079403 Transcript intron_variant - - - - - - rs3865417 18:55989221 A CCDS45876.1 CCDS45876.1 Transcript upstream_gene_variant - - - - - - DISTANCE=451 rs3865417 18:55989221 A 23327 NM_001144971.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078485 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078384 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079394 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079189 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079120 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078281 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078912 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079414 Transcript upstream_gene_variant - - - - - - DISTANCE=1239 rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079255 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079336 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078650 Transcript intron_variant - - - - - - rs3865417 18:55989221 A 23327 NM_001144964.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078807 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078675 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078618 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079179 Transcript intron_variant - - - - - - rs3865417 18:55989221 A 23327 NM_001144970.2 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079265 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078659 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079233 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079324 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079199 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079160 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079027 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078443 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078955 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078925 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079320 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078302 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078350 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078737 Transcript intron_variant - - - - - - rs3865417 18:55989221 A 23327 NM_001243960.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078239 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079077 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079277 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079041 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078253 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078865 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078216 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079311 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079377 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079184 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079023 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079296 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078225 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078833 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078776 Transcript intron_variant - - - - - - rs3865417 18:55989221 A CCDS45874.1 CCDS45874.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078888 Transcript intron_variant - - - - - - rs3865417 18:55989221 A 23327 NM_001144965.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078750 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079202 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079034 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079304 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078268 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078583 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078797 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078318 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078393 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079070 Transcript intron_variant - - - - - - rs3865417 18:55989221 A 23327 NM_015277.5 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078856 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078904 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078606 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079371 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078332 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079393 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079128 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079345 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078490 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078921 Transcript intron_variant - - - - - - rs3865417 18:55989221 A CCDS45872.1 CCDS45872.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A 23327 NM_001144968.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078814 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078680 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079292 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078420 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078986 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079157 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078510 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078504 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078803 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078816 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078667 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079014 Transcript intron_variant - - - - - - rs3865417 18:55989221 A 23327 NM_001144966.2 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079168 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078824 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079147 Transcript intron_variant - - - - - - rs3865417 18:55989221 A 23327 NM_001144969.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079049 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079243 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079137 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078682 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079060 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078946 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078480 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078779 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078292 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079359 Transcript intron_variant - - - - - - rs3865417 18:55989221 A CCDS45875.1 CCDS45875.1 Transcript upstream_gene_variant - - - - - - DISTANCE=451 rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078787 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078760 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079355 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078456 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078271 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078686 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079091 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078434 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078472 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079314 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079164 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078561 Transcript intron_variant - - - - - - rs3865417 18:55989221 A CCDS58632.1 CCDS58632.1 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078768 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079001 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078640 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078593 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079396 Transcript intron_variant - - - - - - rs3865417 18:55989221 A 23327 NM_001144967.2 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078235 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079086 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078464 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079406 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000078935 Transcript intron_variant - - - - - - rs3865417 18:55989221 A ENSESTG00000030971 ENSESTT00000079107 Transcript intron_variant - - - - - - rs11152095 18:56455282 C - - - intergenic_variant - - - - - - rs8094099 18:56455934 G - - - intergenic_variant - - - - - - rs8094236 18:56455983 G - - - intergenic_variant - - - - - - rs6567024 18:56500146 A - - - intergenic_variant - - - - - - rs4940766 18:56508208 A - - - intergenic_variant - - - - - - rs11664723 18:56540638 C ENSESTG00000033480 ENSESTT00000084649 Transcript intron_variant - - - - - - rs11664723 18:56540638 C 55205 NM_018181.4 Transcript intron_variant - - - - - - rs11664723 18:56540638 C ENSESTG00000033480 ENSESTT00000084667 Transcript intron_variant - - - - - - rs11664723 18:56540638 C ENSESTG00000033480 ENSESTT00000084673 Transcript intron_variant - - - - - - rs11664723 18:56540638 C ENSESTG00000033480 ENSESTT00000084640 Transcript intron_variant - - - - - - rs11664723 18:56540638 C ENSESTG00000033480 ENSESTT00000084631 Transcript intron_variant - - - - - - rs11664723 18:56540638 C ENSESTG00000033480 ENSESTT00000084653 Transcript intron_variant - - - - - - rs4940464 18:57173768 T 147372 NM_133459.3 Transcript intron_variant - - - - - - rs4940464 18:57173768 T CCDS32838.1 CCDS32838.1 Transcript intron_variant - - - - - - rs2000891 18:57204829 T 147372 NM_133459.3 Transcript intron_variant - - - - - - rs2000891 18:57204829 T CCDS32838.1 CCDS32838.1 Transcript intron_variant - - - - - - rs4940930 18:57808933 A ENSESTG00000023462 ENSESTT00000059154 Transcript intron_variant - - - - - - rs7234052 18:57919246 A ENSESTG00000023517 ENSESTT00000059255 Transcript intron_variant - - - - - - rs7234052 18:57919246 A ENSESTG00000023517 ENSESTT00000059261 Transcript intron_variant - - - - - - rs7234052 18:57919246 A ENSESTG00000023509 ENSESTT00000059230 Transcript intron_variant - - - - - - rs930884 18:57933098 A ENSESTG00000023517 ENSESTT00000059255 Transcript intron_variant - - - - - - rs930884 18:57933098 A ENSESTG00000023517 ENSESTT00000059261 Transcript intron_variant - - - - - - rs930884 18:57933098 A ENSESTG00000023509 ENSESTT00000059230 Transcript intron_variant - - - - - - rs478847 18:58211164 G - - - intergenic_variant - - - - - - rs10469233 18:58680807 T - - - intergenic_variant - - - - - - rs661125 18:59162908 C 28316 NM_031891.2 Transcript intron_variant - - - - - - rs661125 18:59162908 C ENSESTG00000002406 ENSESTT00000005983 Transcript intron_variant - - - - - - rs661125 18:59162908 C CCDS11977.1 CCDS11977.1 Transcript intron_variant - - - - - - rs11152297 18:59163096 T 28316 NM_031891.2 Transcript intron_variant - - - - - - rs11152297 18:59163096 T ENSESTG00000002406 ENSESTT00000005983 Transcript intron_variant - - - - - - rs11152297 18:59163096 T CCDS11977.1 CCDS11977.1 Transcript intron_variant - - - - - - rs6567217 18:59193075 T 28316 NM_031891.2 Transcript intron_variant - - - - - - rs6567217 18:59193075 T CCDS11977.1 CCDS11977.1 Transcript intron_variant - - - - - - rs9960097 18:59292120 C ENSESTG00000002455 ENSESTT00000006064 Transcript intron_variant - - - - - - rs1452602 18:59295490 A - ENSR00000527168 RegulatoryFeature regulatory_region_variant - - - - - - rs1452602 18:59295490 A ENSESTG00000002455 ENSESTT00000006064 Transcript upstream_gene_variant - - - - - - DISTANCE=185 rs1945474 18:59398268 G - - - intergenic_variant - - - - - - rs4268855 18:59634794 A - - - intergenic_variant - - - - - - rs9959632 18:59805532 C 23556 NM_012327.5 Transcript splice_acceptor_variant - - - - - - rs9959632 18:59805532 C 23556 NM_176787.4 Transcript splice_acceptor_variant - - - - - - rs9959632 18:59805532 C CCDS45879.1 CCDS45879.1 Transcript splice_acceptor_variant - - - - - - rs9959632 18:59805532 C ENSESTG00000003823 ENSESTT00000009639 Transcript 5_prime_UTR_variant 3 - - - - - rs9959632 18:59805532 C ENSESTG00000003823 ENSESTT00000009632 Transcript splice_acceptor_variant - - - - - - rs306227 18:60369807 T - - - intergenic_variant - - - - - - rs6567319 18:60731568 G - - - intergenic_variant - - - - - - rs2849378 18:60966367 C CCDS11981.1 CCDS11981.1 Transcript intron_variant - - - - - - rs2849378 18:60966367 C ENSESTG00000010536 ENSESTT00000026363 Transcript intron_variant - - - - - - rs2849378 18:60966367 C 596 NM_000633.2 Transcript intron_variant - - - - - - rs1541295 18:60983961 T - ENSR00000527414 RegulatoryFeature regulatory_region_variant - - - - - - rs1541295 18:60983961 T CCDS45882.1 CCDS45882.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1321 rs1541295 18:60983961 T CCDS11981.1 CCDS11981.1 Transcript intron_variant - - - - - - rs1541295 18:60983961 T 596 NM_000657.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1226 rs1541295 18:60983961 T ENSESTG00000010536 ENSESTT00000026363 Transcript intron_variant - - - - - - rs1541295 18:60983961 T 596 NM_000633.2 Transcript intron_variant - - - - - - rs6567392 18:61461573 T CCDS58633.1 CCDS58633.1 Transcript intron_variant - - - - - - rs6567392 18:61461573 T 8710 NM_001261831.1 Transcript intron_variant - - - - - - rs6567392 18:61461573 T ENSESTG00000010310 ENSESTT00000025789 Transcript downstream_gene_variant - - - - - - DISTANCE=1085 rs6567392 18:61461573 T 8710 NM_003784.3 Transcript intron_variant - - - - - - rs6567392 18:61461573 T 8710 NM_001040147.2 Transcript intron_variant - - - - - - rs6567392 18:61461573 T ENSESTG00000010310 ENSESTT00000025801 Transcript intron_variant - - - - - - rs6567392 18:61461573 T ENSESTG00000010310 ENSESTT00000025804 Transcript intron_variant - - - - - - rs6567392 18:61461573 T CCDS11988.1 CCDS11988.1 Transcript intron_variant - - - - - - rs6567392 18:61461573 T 8710 NM_001261830.1 Transcript intron_variant - - - - - - rs213077 18:61680561 C - - - intergenic_variant - - - - - - rs1944274 18:61753054 C 221241 NR_027245.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1517171 18:61783667 A 284294 NR_033881.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1517171 18:61783667 A 221241 NR_027245.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9946899 18:62031071 G 284294 NR_033881.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4536560 18:62208590 G - - - intergenic_variant - - - - - - rs11661521 18:62249715 T - - - intergenic_variant - - - - - - rs2959438 18:62271261 T - - - intergenic_variant - - - - - - rs1348054 18:62571336 T - - - intergenic_variant - - - - - - rs7233338 18:62591221 C - - - intergenic_variant - - - - - - rs2957235 18:62725681 C - - - intergenic_variant - - - - - - rs666385 18:62924985 A - - - intergenic_variant - - - - - - rs557507 18:62925166 G - - - intergenic_variant - - - - - - rs4941344 18:63228962 C - - - intergenic_variant - - - - - - rs2541862 18:63612021 G - - - intergenic_variant - - - - - - rs2715336 18:63667867 C - - - intergenic_variant - - - - - - rs2193293 18:63755181 A - - - intergenic_variant - - - - - - rs2541830 18:63775849 A - - - intergenic_variant - - - - - - rs6566204 18:64001282 T - - - intergenic_variant - - - - - - rs2457668 18:64113854 G - - - intergenic_variant - - - - - - rs4584935 18:64350189 C - ENSR00000527647 RegulatoryFeature regulatory_region_variant - - - - - - rs4584935 18:64350189 C - - - intergenic_variant - - - - - - rs4629080 18:64703163 T - - - intergenic_variant - - - - - - rs4402670 18:64873361 G - - - intergenic_variant - - - - - - rs188141 18:65261299 T 643542 NR_033921.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4243304 18:65675723 G - - - intergenic_variant - - - - - - rs12454581 18:65743916 C - - - intergenic_variant - - - - - - rs1943054 18:65823695 G - - - intergenic_variant - - - - - - rs76195946 18:65831788 G - - - intergenic_variant - - - - - - rs522333 18:66033732 A - - - intergenic_variant - - - - - - rs11151444 18:66127580 G - - - intergenic_variant - - - - - - rs2676317 18:66197049 C ENSESTG00000018912 ENSESTT00000047603 Transcript intron_variant - - - - - - rs2000898 18:66633680 G CCDS11996.2 CCDS11996.2 Transcript intron_variant - - - - - - rs2000898 18:66633680 G 79839 NM_024781.2 Transcript intron_variant - - - - - - rs2000898 18:66633680 G ENSESTG00000006277 ENSESTT00000015816 Transcript intron_variant - - - - - - rs2000898 18:66633680 G 79839 NM_001093729.1 Transcript intron_variant - - - - - - rs1594472 18:66745729 C - - - intergenic_variant - - - - - - rs2032242 18:66797379 T - - - intergenic_variant - - - - - - rs4299250 18:66819907 C - - - intergenic_variant - - - - - - rs535109 18:66867308 A - - - intergenic_variant - - - - - - rs8090301 18:66933028 C - - - intergenic_variant - - - - - - rs4891738 18:66998680 A - - - intergenic_variant - - - - - - rs356000 18:67058882 G - - - intergenic_variant - - - - - - rs12607362 18:67434711 G ENSESTG00000022620 ENSESTT00000057135 Transcript intron_variant - - - - - - rs12607362 18:67434711 G CCDS32841.1 CCDS32841.1 Transcript intron_variant - - - - - - rs12607362 18:67434711 G ENSESTG00000022620 ENSESTT00000057119 Transcript intron_variant - - - - - - rs12607362 18:67434711 G 220164 NM_152721.5 Transcript intron_variant - - - - - - rs481014 18:67610367 C - ENSR00000527858 RegulatoryFeature regulatory_region_variant - - - - - - rs481014 18:67610367 C CCDS11997.1 CCDS11997.1 Transcript intron_variant - - - - - - rs481014 18:67610367 C 10666 NM_006566.2 Transcript intron_variant - - - - - - rs481014 18:67610367 C ENSESTG00000022841 ENSESTT00000057586 Transcript intron_variant - - - - - - rs285225 18:67712622 C 25914 NM_173630.3 Transcript intron_variant - - - - - - rs285225 18:67712622 C ENSESTG00000022695 ENSESTT00000057507 Transcript intron_variant - - - - - - rs285225 18:67712622 C CCDS42443.1 CCDS42443.1 Transcript intron_variant - - - - - - rs9950626 18:68054184 G - - - intergenic_variant - - - - - - rs4891856 18:68096201 A - - - intergenic_variant - - - - - - rs11151618 18:68526225 T - - - intergenic_variant - - - - - - rs1942168 18:68676589 G - - - intergenic_variant - - - - - - rs1942190 18:68680339 C - ENSR00000527961 RegulatoryFeature regulatory_region_variant - - - - - - rs1942190 18:68680339 C - - - intergenic_variant - - - - - - rs1942203 18:68708936 C - - - intergenic_variant - - - - - - rs1942171 18:68732007 A ENSESTG00000009288 ENSESTT00000023271 Transcript intron_variant - - - - - - rs2051282 18:68751269 T ENSESTG00000009288 ENSESTT00000023271 Transcript intron_variant - - - - - - rs10153394 18:68788905 T ENSESTG00000009288 ENSESTT00000023271 Transcript intron_variant - - - - - - rs6566518 18:68863972 C ENSESTG00000009288 ENSESTT00000023271 Transcript intron_variant - - - - - - rs670940 18:70187890 T - - - intergenic_variant - - - - - - rs636527 18:70188009 G - - - intergenic_variant - - - - - - rs8083277 18:70575542 A - - - intergenic_variant - - - - - - rs2432838 18:70662095 A - - - intergenic_variant - - - - - - rs805074 18:70817560 G - ENSR00000528048 RegulatoryFeature regulatory_region_variant - - - - - - rs805074 18:70817560 G 400655 NR_034133.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3733 rs805075 18:70817722 G - ENSR00000528048 RegulatoryFeature regulatory_region_variant - - - - - - rs805075 18:70817722 G 400655 NR_034133.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3571 rs10871713 18:70817866 G 400655 NR_034133.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3427 rs805076 18:70817876 G 400655 NR_034133.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3417 rs805079 18:70817935 G 400655 NR_034133.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3358 rs809791 18:70818048 G 400655 NR_034133.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3245 rs2654164 18:70818300 G - ENSR00000528049 RegulatoryFeature regulatory_region_variant - - - - - - rs2654164 18:70818300 G 400655 NR_034133.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2993 rs4335851 18:70875256 C 400655 NR_034133.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4243336 18:70985958 G - ENSR00000528063 RegulatoryFeature regulatory_region_variant - - - - - - rs4243336 18:70985958 G - - - intergenic_variant - - - - - - rs1942724 18:71155707 C - - - intergenic_variant - - - - - - rs7237499 18:71765942 A ENSESTG00000028365 ENSESTT00000071308 Transcript intron_variant - - - - - - rs7237499 18:71765942 A 201456 NM_152676.2 Transcript intron_variant - - - - - - rs7237499 18:71765942 A CCDS45884.1 CCDS45884.1 Transcript intron_variant - - - - - - rs7237499 18:71765942 A ENSESTG00000028365 ENSESTT00000071360 Transcript intron_variant - - - - - - rs7237499 18:71765942 A 201456 NM_001142958.1 Transcript intron_variant - - - - - - rs1790857 18:71959515 A - ENSR00000528170 RegulatoryFeature regulatory_region_variant - - - - - - rs1790857 18:71959515 A CCDS12005.1 CCDS12005.1 Transcript upstream_gene_variant - - - - - - DISTANCE=405 rs1790857 18:71959515 A ENSESTG00000028224 ENSESTT00000070950 Transcript downstream_gene_variant - - - - - - DISTANCE=3330 rs1790857 18:71959515 A ENSESTG00000028248 ENSESTT00000071137 Transcript upstream_gene_variant - - - - - - DISTANCE=345 rs1790857 18:71959515 A CCDS54188.1 CCDS54188.1 Transcript upstream_gene_variant - - - - - - DISTANCE=405 rs1790857 18:71959515 A ENSESTG00000028248 ENSESTT00000071111 Transcript upstream_gene_variant - - - - - - DISTANCE=335 rs1790857 18:71959515 A 1528 NM_001914.3 Transcript upstream_gene_variant - - - - - - DISTANCE=264 rs1790857 18:71959515 A 1528 NM_001190807.2 Transcript upstream_gene_variant - - - - - - DISTANCE=264 rs1790857 18:71959515 A ENSESTG00000028248 ENSESTT00000071164 Transcript upstream_gene_variant - - - - - - DISTANCE=1239 rs1790857 18:71959515 A 1528 NM_148923.3 Transcript upstream_gene_variant - - - - - - DISTANCE=264 rs1790857 18:71959515 A CCDS12004.1 CCDS12004.1 Transcript upstream_gene_variant - - - - - - DISTANCE=405 rs2639965 18:72859808 A - - - intergenic_variant - - - - - - rs8092492 18:73211461 G - - - intergenic_variant - - - - - - rs4447512 18:73224634 C - - - intergenic_variant - - - - - - rs4324219 18:73406136 G ENSESTG00000018757 ENSESTT00000047295 Transcript downstream_gene_variant - - - - - - DISTANCE=3224 rs2612386 18:73586904 G - - - intergenic_variant - - - - - - rs2660819 18:73678783 C - - - intergenic_variant - - - - - - rs193326 18:73778647 C - - - intergenic_variant - - - - - - rs4891150 18:73946045 A - ENSR00000528329 RegulatoryFeature regulatory_region_variant - - - - - - rs4891150 18:73946045 A ENSESTG00000033590 ENSESTT00000084905 Transcript intron_variant - - - - - - rs11150945 18:74043146 C ENSESTG00000033590 ENSESTT00000084905 Transcript intron_variant - - - - - - rs9965640 18:74180055 G - ENSR00000528367 RegulatoryFeature regulatory_region_variant - - - - - - rs9965640 18:74180055 G ENSESTG00000009783 ENSESTT00000024483 Transcript intron_variant - - - - - - rs9965640 18:74180055 G 9658 NM_014643.3 Transcript intron_variant - - - - - - rs9964541 18:74188490 C ENSESTG00000009783 ENSESTT00000024483 Transcript intron_variant - - - - - - rs9964541 18:74188490 C 9658 NM_014643.3 Transcript intron_variant - - - - - - rs690419 18:74191768 C ENSESTG00000009783 ENSESTT00000024483 Transcript intron_variant - - - - - - rs690419 18:74191768 C 9658 NM_014643.3 Transcript intron_variant - - - - - - rs7241475 18:74224206 G - - - intergenic_variant - - - - - - rs2174898 18:74247395 C 284276 NR_015417.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2174898 18:74247395 C ENSESTG00000009598 ENSESTT00000024069 Transcript intron_variant - - - - - - rs2174898 18:74247395 C ENSESTG00000009598 ENSESTT00000024073 Transcript intron_variant - - - - - - rs2174898 18:74247395 C ENSESTG00000009598 ENSESTT00000024070 Transcript intron_variant - - - - - - rs2174898 18:74247395 C ENSESTG00000009598 ENSESTT00000024077 Transcript intron_variant - - - - - - rs6565893 18:74272690 G 284276 NR_015417.1 Transcript downstream_gene_variant - - - - - - DISTANCE=906 rs6565893 18:74272690 G ENSESTG00000009598 ENSESTT00000024069 Transcript downstream_gene_variant - - - - - - DISTANCE=2151 rs6565893 18:74272690 G ENSESTG00000009598 ENSESTT00000024079 Transcript downstream_gene_variant - - - - - - DISTANCE=2151 rs6565893 18:74272690 G ENSESTG00000009598 ENSESTT00000024073 Transcript intron_variant - - - - - - rs6565893 18:74272690 G ENSESTG00000009598 ENSESTT00000024070 Transcript downstream_gene_variant - - - - - - DISTANCE=2151 rs6565893 18:74272690 G ENSESTG00000009598 ENSESTT00000024077 Transcript intron_variant - - - - - - rs9960046 18:74317438 C ENSESTG00000009598 ENSESTT00000024073 Transcript intron_variant - - - - - - rs12956572 18:74730216 C ENSESTG00000009714 ENSESTT00000024467 Transcript intron_variant - - - - - - rs12956572 18:74730216 C CCDS42450.1 CCDS42450.1 Transcript intron_variant - - - - - - rs12956572 18:74730216 C ENSESTG00000009714 ENSESTT00000024384 Transcript intron_variant - - - - - - rs12956572 18:74730216 C CCDS42449.1 CCDS42449.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1252 rs12956572 18:74730216 C 4155 NM_001025081.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1161 rs12956572 18:74730216 C 4155 NM_002385.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1161 rs12956572 18:74730216 C ENSESTG00000009714 ENSESTT00000024382 Transcript intron_variant - - - - - - rs12956572 18:74730216 C ENSESTG00000009660 ENSESTT00000024227 Transcript downstream_gene_variant - - - - - - DISTANCE=1175 rs12956572 18:74730216 C 4155 NM_001025090.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1161 rs12956572 18:74730216 C ENSESTG00000009714 ENSESTT00000024418 Transcript intron_variant - - - - - - rs12956572 18:74730216 C ENSESTG00000009714 ENSESTT00000024369 Transcript intron_variant - - - - - - rs12956572 18:74730216 C ENSESTG00000009714 ENSESTT00000024459 Transcript intron_variant - - - - - - rs12956572 18:74730216 C CCDS12011.1 CCDS12011.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1252 rs12956572 18:74730216 C CCDS42448.1 CCDS42448.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1252 rs12956572 18:74730216 C ENSESTG00000009714 ENSESTT00000024432 Transcript intron_variant - - - - - - rs12956572 18:74730216 C ENSESTG00000009714 ENSESTT00000024381 Transcript intron_variant - - - - - - rs12956572 18:74730216 C 4155 NM_001025101.1 Transcript intron_variant - - - - - - rs12956572 18:74730216 C CCDS32847.1 CCDS32847.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1252 rs12956572 18:74730216 C ENSESTG00000009714 ENSESTT00000024342 Transcript intron_variant - - - - - - rs12956572 18:74730216 C 4155 NM_001025100.1 Transcript intron_variant - - - - - - rs12956572 18:74730216 C 4155 NM_001025092.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1161 rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024352 Transcript downstream_gene_variant - - - - - - DISTANCE=1632 rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024467 Transcript intron_variant - - - - - - rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024418 Transcript intron_variant - - - - - - rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024459 Transcript intron_variant - - - - - - rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024369 Transcript intron_variant - - - - - - rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024432 Transcript intron_variant - - - - - - rs538222 18:74776653 G CCDS42450.1 CCDS42450.1 Transcript intron_variant - - - - - - rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024384 Transcript intron_variant - - - - - - rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024381 Transcript intron_variant - - - - - - rs538222 18:74776653 G 4155 NM_001025101.1 Transcript intron_variant - - - - - - rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024382 Transcript intron_variant - - - - - - rs538222 18:74776653 G 4155 NM_001025100.1 Transcript intron_variant - - - - - - rs538222 18:74776653 G ENSESTG00000009714 ENSESTT00000024342 Transcript intron_variant - - - - - - rs7242619 18:75534542 C - - - intergenic_variant - - - - - - rs4429375 18:75834802 G - - - intergenic_variant - - - - - - rs9961007 18:75836142 G - - - intergenic_variant - - - - - - rs9961011 18:75836162 T - - - intergenic_variant - - - - - - rs6506829 18:76045460 A - - - intergenic_variant - - - - - - rs6506831 18:76069335 T - - - intergenic_variant - - - - - - rs117252532 18:76209164 A - - - intergenic_variant - - - - - - rs1866333 18:76378218 C - - - intergenic_variant - - - - - - rs4798976 18:76466796 G - - - intergenic_variant - - - - - - rs2941775 18:76485684 C - - - intergenic_variant - - - - - - rs1972092 18:76499659 C - - - intergenic_variant - - - - - - rs907287 18:76574710 C - ENSR00000528537 RegulatoryFeature regulatory_region_variant - - - - - - rs907287 18:76574710 C - - - intergenic_variant - - - - - - rs160190 18:77230166 C 4772 NM_006162.3 Transcript intron_variant - - - - - - rs160190 18:77230166 C CCDS12015.1 CCDS12015.1 Transcript intron_variant - - - - - - rs160190 18:77230166 C 4772 NM_172390.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1989 rs160190 18:77230166 C ENSESTG00000006780 ENSESTT00000017277 Transcript intron_variant - - - - - - rs160190 18:77230166 C CCDS32850.1 CCDS32850.1 Transcript intron_variant - - - - - - rs160190 18:77230166 C CCDS12016.1 CCDS12016.1 Transcript intron_variant - - - - - - rs160190 18:77230166 C ENSESTG00000006780 ENSESTT00000017282 Transcript intron_variant - - - - - - rs160190 18:77230166 C 4772 NM_172388.1 Transcript intron_variant - - - - - - rs160190 18:77230166 C ENSESTG00000006780 ENSESTT00000017293 Transcript downstream_gene_variant - - - - - - DISTANCE=2165 rs160190 18:77230166 C 4772 NM_172389.1 Transcript intron_variant - - - - - - rs160190 18:77230166 C 4772 NM_172387.1 Transcript intron_variant - - - - - - rs584982 18:77327450 A - - - intergenic_variant - - - - - - rs4799074 18:77393165 C - - - intergenic_variant - - - - - - rs4799107 18:77671114 C ENSESTG00000007212 ENSESTT00000018215 Transcript intron_variant - - - - - - rs4799107 18:77671114 C 80148 NM_025078.4 Transcript intron_variant - - - - - - rs4799107 18:77671114 C ENSESTG00000007212 ENSESTT00000018209 Transcript intron_variant - - - - - - rs4799107 18:77671114 C CCDS12020.1 CCDS12020.1 Transcript intron_variant - - - - - - rs4799107 18:77671114 C 80148 NM_001146345.1 Transcript intron_variant - - - - - - rs4799107 18:77671114 C ENSESTG00000007212 ENSESTT00000018225 Transcript intron_variant - - - - - - rs4799107 18:77671114 C CCDS54193.1 CCDS54193.1 Transcript intron_variant - - - - - - rs4799107 18:77671114 C CCDS54192.1 CCDS54192.1 Transcript intron_variant - - - - - - rs4799107 18:77671114 C ENSESTG00000007212 ENSESTT00000018217 Transcript intron_variant - - - - - - rs4799107 18:77671114 C 80148 NM_001146343.1 Transcript intron_variant - - - - - - rs9963291 18:77687816 C - ENSR00001516644 RegulatoryFeature regulatory_region_variant - - - - - - rs9963291 18:77687816 C ENSESTG00000007212 ENSESTT00000018215 Transcript intron_variant - - - - - - rs9963291 18:77687816 C 80148 NM_025078.4 Transcript intron_variant - - - - - - rs9963291 18:77687816 C ENSESTG00000007212 ENSESTT00000018209 Transcript intron_variant - - - - - - rs9963291 18:77687816 C CCDS12020.1 CCDS12020.1 Transcript intron_variant - - - - - - rs9963291 18:77687816 C 80148 NM_001146345.1 Transcript intron_variant - - - - - - rs9963291 18:77687816 C ENSESTG00000007212 ENSESTT00000018225 Transcript intron_variant - - - - - - rs9963291 18:77687816 C ENSESTG00000007212 ENSESTT00000018213 Transcript intron_variant - - - - - - rs9963291 18:77687816 C CCDS54193.1 CCDS54193.1 Transcript intron_variant - - - - - - rs9963291 18:77687816 C CCDS54192.1 CCDS54192.1 Transcript intron_variant - - - - - - rs9963291 18:77687816 C ENSESTG00000007212 ENSESTT00000018217 Transcript intron_variant - - - - - - rs9963291 18:77687816 C 80148 NM_001146343.1 Transcript intron_variant - - - - - - rs9961192 18:77897719 G ENSESTG00000007032 ENSESTT00000017852 Transcript downstream_gene_variant - - - - - - DISTANCE=2895 rs9961192 18:77897719 G CCDS32853.1 CCDS32853.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1027 rs9961192 18:77897719 G ENSESTG00000007032 ENSESTT00000017833 Transcript downstream_gene_variant - - - - - - DISTANCE=2895 rs9961192 18:77897719 G 22850 NM_014913.3 Transcript 3_prime_UTR_variant 4878 - - - - - rs6417053 18:77949564 T ENSESTG00000007117 ENSESTT00000017990 Transcript intron_variant - - - - - - rs6417053 18:77949564 T 84552 NM_032510.3 Transcript intron_variant - - - - - - rs6417053 18:77949564 T ENSESTG00000007117 ENSESTT00000017993 Transcript intron_variant - - - - - - rs6417053 18:77949564 T CCDS12022.1 CCDS12022.1 Transcript intron_variant - - - - - - rs6417053 18:77949564 T ENSESTG00000007117 ENSESTT00000017985 Transcript intron_variant - - - - - - rs11666936 19:614837 G ENSESTG00000023815 ENSESTT00000060164 Transcript intron_variant - - - - - - rs11666936 19:614837 G 610 NM_001194.3 Transcript intron_variant - - - - - - rs11666936 19:614837 G CCDS12035.1 CCDS12035.1 Transcript intron_variant - - - - - - rs11666936 19:614837 G 5442 NM_005035.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2386 rs11666936 19:614837 G CCDS12036.1 CCDS12036.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2437 rs12976506 19:748084 G - ENSR00000341262 RegulatoryFeature regulatory_region_variant - - - - - - rs12976506 19:748084 G ENSESTG00000024035 ENSESTT00000060726 Transcript upstream_gene_variant - - - - - - DISTANCE=3041 rs12976506 19:748084 G 5064 NM_002579.2 Transcript 3_prime_UTR_variant 2628 - - - - - rs12976506 19:748084 G ENSESTG00000023947 ENSESTT00000060667 Transcript downstream_gene_variant - - - - - - DISTANCE=1254 rs12976506 19:748084 G ENSESTG00000023947 ENSESTT00000060654 Transcript downstream_gene_variant - - - - - - DISTANCE=1254 rs12976506 19:748084 G 126353 NM_173481.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3062 rs12976506 19:748084 G CCDS32858.1 CCDS32858.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1270 rs12976506 19:748084 G ENSESTG00000023947 ENSESTT00000060630 Transcript downstream_gene_variant - - - - - - DISTANCE=1254 rs12976506 19:748084 G CCDS32857.1 CCDS32857.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1270 rs12976506 19:748084 G 5064 NM_001040134.1 Transcript 3_prime_UTR_variant 2496 - - - - - rs12976506 19:748084 G ENSESTG00000025461 ENSESTT00000064216 Transcript upstream_gene_variant - - - - - - DISTANCE=1191 rs12976506 19:748084 G ENSESTG00000023947 ENSESTT00000060510 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs62132298 19:844822 C - ENSR00001417230 RegulatoryFeature regulatory_region_variant - - - - - - rs62132298 19:844822 C 5657 NM_002777.3 Transcript intron_variant - - - - - - rs62132298 19:844822 C ENSESTG00000024238 ENSESTT00000061308 Transcript intron_variant - - - - - - rs62132298 19:844822 C CCDS32860.1 CCDS32860.1 Transcript intron_variant - - - - - - rs1875962 19:1537608 T ENSESTG00000015869 ENSESTT00000039818 Transcript downstream_gene_variant - - - - - - DISTANCE=2153 rs1875962 19:1537608 T 126520 NM_001243079.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2153 rs1875962 19:1537608 T ENSESTG00000015869 ENSESTT00000039808 Transcript downstream_gene_variant - - - - - - DISTANCE=2427 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031701 Transcript downstream_gene_variant - - - - - - DISTANCE=810 rs11882359 19:1609267 G ENSESTG00000015889 ENSESTT00000039850 Transcript upstream_gene_variant - - - - - - DISTANCE=26 rs11882359 19:1609267 G 6929 NM_001136139.2 Transcript downstream_gene_variant - - - - - - DISTANCE=22 rs11882359 19:1609267 G ENSESTG00000012662 ENSESTT00000031800 Transcript upstream_gene_variant - - - - - - DISTANCE=3825 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031715 Transcript downstream_gene_variant - - - - - - DISTANCE=2206 rs11882359 19:1609267 G 6929 NM_003200.3 Transcript downstream_gene_variant - - - - - - DISTANCE=22 rs11882359 19:1609267 G CCDS12074.1 CCDS12074.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2439 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031694 Transcript downstream_gene_variant - - - - - - DISTANCE=2206 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031742 Transcript downstream_gene_variant - - - - - - DISTANCE=2538 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031739 Transcript downstream_gene_variant - - - - - - DISTANCE=2206 rs11882359 19:1609267 G 10975 NM_006830.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3784 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031736 Transcript downstream_gene_variant - - - - - - DISTANCE=2150 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031667 Transcript downstream_gene_variant - - - - - - DISTANCE=2150 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031730 Transcript downstream_gene_variant - - - - - - DISTANCE=810 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031656 Transcript downstream_gene_variant - - - - - - DISTANCE=810 rs11882359 19:1609267 G CCDS12073.1 CCDS12073.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3859 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031698 Transcript downstream_gene_variant - - - - - - DISTANCE=2538 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031712 Transcript downstream_gene_variant - - - - - - DISTANCE=2150 rs11882359 19:1609267 G ENSESTG00000012662 ENSESTT00000031779 Transcript upstream_gene_variant - - - - - - DISTANCE=3821 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031706 Transcript downstream_gene_variant - - - - - - DISTANCE=1168 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031662 Transcript downstream_gene_variant - - - - - - DISTANCE=1168 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031749 Transcript downstream_gene_variant - - - - - - DISTANCE=1704 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031716 Transcript downstream_gene_variant - - - - - - DISTANCE=2538 rs11882359 19:1609267 G CCDS45899.1 CCDS45899.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2439 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031674 Transcript downstream_gene_variant - - - - - - DISTANCE=2206 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031731 Transcript downstream_gene_variant - - - - - - DISTANCE=1168 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031677 Transcript downstream_gene_variant - - - - - - DISTANCE=2538 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031691 Transcript downstream_gene_variant - - - - - - DISTANCE=2150 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031685 Transcript downstream_gene_variant - - - - - - DISTANCE=810 rs11882359 19:1609267 G ENSESTG00000012606 ENSESTT00000031687 Transcript downstream_gene_variant - - - - - - DISTANCE=1168 rs10425308 19:1695056 T - - - intergenic_variant - - - - - - rs6510625 19:1793979 G 148229 NM_138813.3 Transcript intron_variant - - - - - - rs6510625 19:1793979 G CCDS54196.1 CCDS54196.1 Transcript intron_variant - - - - - - rs6510625 19:1793979 G 148229 NR_047593.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6510625 19:1793979 G 148229 NM_001178002.2 Transcript intron_variant - - - - - - rs6510625 19:1793979 G ENSESTG00000015893 ENSESTT00000039856 Transcript upstream_gene_variant - - - - - - DISTANCE=935 rs6510625 19:1793979 G CCDS45901.1 CCDS45901.1 Transcript intron_variant - - - - - - rs2854111 19:2270207 G - ENSR00000341757 RegulatoryFeature regulatory_region_variant - - - - - - rs2854111 19:2270207 G 374872 NM_198532.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4424 rs2854111 19:2270207 G ENSESTG00000013983 ENSESTT00000034976 Transcript upstream_gene_variant - - - - - - DISTANCE=91 rs2854111 19:2270207 G 4946 NM_004152.2 Transcript intron_variant - - - - - - rs2854111 19:2270207 G CCDS58639.1 CCDS58639.1 Transcript intron_variant - - - - - - rs2854111 19:2270207 G ENSESTG00000013995 ENSESTT00000035022 Transcript upstream_gene_variant - - - - - - DISTANCE=1661 rs4806865 19:2542058 G ENSESTG00000014642 ENSESTT00000036683 Transcript intron_variant - - - - - - rs4806865 19:2542058 G ENSESTG00000014642 ENSESTT00000036679 Transcript intron_variant - - - - - - rs4806865 19:2542058 G ENSESTG00000014642 ENSESTT00000036673 Transcript intron_variant - - - - - - rs4806865 19:2542058 G 2788 NM_052847.2 Transcript intron_variant - - - - - - rs8105330 19:2753566 G CCDS12094.1 CCDS12094.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3775 rs8105330 19:2753566 G ENSESTG00000014443 ENSESTT00000036213 Transcript downstream_gene_variant - - - - - - DISTANCE=2034 rs8105330 19:2753566 G 6449 NM_003021.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1146 rs439808 19:2994814 C - ENSR00000640735 RegulatoryFeature regulatory_region_variant - - - - - - rs439808 19:2994814 C ENSESTG00000019294 ENSESTT00000048844 Transcript downstream_gene_variant - - - - - - DISTANCE=2826 rs439808 19:2994814 C ENSESTG00000019294 ENSESTT00000048857 Transcript downstream_gene_variant - - - - - - DISTANCE=2831 rs439808 19:2994814 C CCDS45912.1 CCDS45912.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3032 rs439808 19:2994814 C CCDS45913.1 CCDS45913.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3108 rs439808 19:2994814 C CCDS45910.1 CCDS45910.1 Transcript intron_variant - - - - - - rs439808 19:2994814 C CCDS12100.1 CCDS12100.1 Transcript intron_variant - - - - - - rs439808 19:2994814 C 7089 NM_001144761.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2822 rs439808 19:2994814 C ENSESTG00000017611 ENSESTT00000044381 Transcript intron_variant - - - - - - rs439808 19:2994814 C ENSESTG00000019294 ENSESTT00000048851 Transcript downstream_gene_variant - - - - - - DISTANCE=2826 rs439808 19:2994814 C 7089 NM_003260.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2822 rs439808 19:2994814 C ENSESTG00000017611 ENSESTT00000044372 Transcript intron_variant - - - - - - rs439808 19:2994814 C ENSESTG00000017611 ENSESTT00000044366 Transcript intron_variant - - - - - - rs439808 19:2994814 C ENSESTG00000019294 ENSESTT00000048578 Transcript downstream_gene_variant - - - - - - DISTANCE=2826 rs439808 19:2994814 C 79816 NM_024760.2 Transcript intron_variant - - - - - - rs439808 19:2994814 C ENSESTG00000019294 ENSESTT00000048735 Transcript downstream_gene_variant - - - - - - DISTANCE=2826 rs439808 19:2994814 C 79816 NM_001143986.1 Transcript intron_variant - - - - - - rs439808 19:2994814 C CCDS45911.1 CCDS45911.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3032 rs439808 19:2994814 C 7089 NM_001144762.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2822 rs439808 19:2994814 C ENSESTG00000019294 ENSESTT00000048824 Transcript downstream_gene_variant - - - - - - DISTANCE=2831 rs308041 19:3121609 C ENSESTG00000017631 ENSESTT00000044539 Transcript downstream_gene_variant - - - - - - DISTANCE=157 rs308041 19:3121609 C CCDS12103.1 CCDS12103.1 Transcript downstream_gene_variant - - - - - - DISTANCE=432 rs308041 19:3121609 C ENSESTG00000017631 ENSESTT00000044529 Transcript downstream_gene_variant - - - - - - DISTANCE=157 rs308041 19:3121609 C 2767 NM_002067.2 Transcript downstream_gene_variant - - - - - - DISTANCE=141 rs308041 19:3121609 C ENSESTG00000017631 ENSESTT00000044509 Transcript downstream_gene_variant - - - - - - DISTANCE=157 rs310680 19:3150238 G CCDS12104.1 CCDS12104.1 Transcript missense_variant 440 440 147 Y/C tAc/tGc - PolyPhen=benign;SIFT=tolerated rs310680 19:3150238 G ENSESTG00000017687 ENSESTT00000044638 Transcript missense_variant 638 257 86 Y/C tAc/tGc - rs310680 19:3150238 G ENSESTG00000017687 ENSESTT00000044573 Transcript downstream_gene_variant - - - - - - DISTANCE=1472 rs310680 19:3150238 G 2769 NM_002068.2 Transcript missense_variant 698 440 147 Y/C tAc/tGc - PolyPhen=benign;SIFT=tolerated rs310680 19:3150238 G ENSESTG00000019105 ENSESTT00000048041 Transcript intron_variant - - - - - - rs532666 19:3188169 C CCDS32869.1 CCDS32869.1 Transcript intron_variant - - - - - - rs532666 19:3188169 C ENSESTG00000017737 ENSESTT00000044931 Transcript intron_variant - - - - - - rs532666 19:3188169 C ENSESTG00000017737 ENSESTT00000044933 Transcript intron_variant - - - - - - rs532666 19:3188169 C 56926 NM_020170.3 Transcript intron_variant - - - - - - rs2159323 19:3444372 G - ENSR00000342048 RegulatoryFeature regulatory_region_variant - - - - - - rs2159323 19:3444372 G 4782 NM_001245004.1 Transcript intron_variant - - - - - - rs2159323 19:3444372 G ENSESTG00000017923 ENSESTT00000045260 Transcript intron_variant - - - - - - rs2159323 19:3444372 G 4782 NM_001245005.1 Transcript intron_variant - - - - - - rs2159323 19:3444372 G CCDS45914.1 CCDS45914.1 Transcript intron_variant - - - - - - rs2159323 19:3444372 G ENSESTG00000017923 ENSESTT00000045265 Transcript intron_variant - - - - - - rs2159323 19:3444372 G 4782 NM_005597.3 Transcript intron_variant - - - - - - rs2159323 19:3444372 G CCDS12107.1 CCDS12107.1 Transcript intron_variant - - - - - - rs2159323 19:3444372 G 4782 NM_001245002.1 Transcript intron_variant - - - - - - rs2159323 19:3444372 G 4782 NM_205843.2 Transcript intron_variant - - - - - - rs2159323 19:3444372 G CCDS58640.1 CCDS58640.1 Transcript intron_variant - - - - - - rs10417031 19:3469002 C 4782 NM_001245004.1 Transcript 3_prime_UTR_variant 7678 - - - - - rs10417031 19:3469002 C 4782 NM_001245005.1 Transcript 3_prime_UTR_variant 7701 - - - - - rs10417031 19:3469002 C 4782 NM_005597.3 Transcript 3_prime_UTR_variant 7592 - - - - - rs10417031 19:3469002 C 4782 NM_205843.2 Transcript 3_prime_UTR_variant 7855 - - - - - rs10417031 19:3469002 C 4782 NM_001245002.1 Transcript 3_prime_UTR_variant 7832 - - - - - rs10417031 19:3469002 C ENSESTG00000017989 ENSESTT00000045285 Transcript downstream_gene_variant - - - - - - DISTANCE=3611 rs7258234 19:3539444 G - ENSR00000342080 RegulatoryFeature regulatory_region_variant - - - - - - rs7258234 19:3539444 G CCDS12109.1 CCDS12109.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4610 rs7258234 19:3539444 G 51343 NM_016263.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2689 rs7258234 19:3539444 G ENSESTG00000018001 ENSESTT00000045458 Transcript downstream_gene_variant - - - - - - DISTANCE=3895 rs7258234 19:3539444 G 126321 NM_001042680.1 Transcript intron_variant - - - - - - rs7258234 19:3539444 G CCDS45916.1 CCDS45916.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4610 rs7258234 19:3539444 G ENSESTG00000018114 ENSESTT00000045593 Transcript upstream_gene_variant - - - - - - DISTANCE=4776 rs7258234 19:3539444 G CCDS42464.1 CCDS42464.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3335 rs7258234 19:3539444 G 51343 NM_001136197.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2689 rs7258234 19:3539444 G CCDS42463.1 CCDS42463.1 Transcript intron_variant - - - - - - rs7258234 19:3539444 G 126321 NM_021731.2 Transcript intron_variant - - - - - - rs7258234 19:3539444 G ENSESTG00000018102 ENSESTT00000045571 Transcript upstream_gene_variant - - - - - - DISTANCE=3800 rs7258234 19:3539444 G ENSESTG00000018001 ENSESTT00000045542 Transcript downstream_gene_variant - - - - - - DISTANCE=3895 rs7258234 19:3539444 G 51343 NM_001136198.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2689 rs7258234 19:3539444 G CCDS45918.1 CCDS45918.1 Transcript intron_variant - - - - - - rs7258234 19:3539444 G CCDS45917.1 CCDS45917.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4610 rs7258234 19:3539444 G 100128569 NM_001135580.1 Transcript intron_variant - - - - - - rs7258234 19:3539444 G ENSESTG00000018001 ENSESTT00000045523 Transcript downstream_gene_variant - - - - - - DISTANCE=3895 rs7258234 19:3539444 G 126321 NM_174983.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4753 rs7257360 19:3667461 C CCDS32872.1 CCDS32872.1 Transcript intron_variant - - - - - - rs7257360 19:3667461 C ENSESTG00000018760 ENSESTT00000047461 Transcript intron_variant - - - - - - rs7257360 19:3667461 C ENSESTG00000018760 ENSESTT00000047468 Transcript intron_variant - - - - - - rs7257360 19:3667461 C 23396 NM_001195733.1 Transcript intron_variant - - - - - - rs7257360 19:3667461 C ENSESTG00000018760 ENSESTT00000047475 Transcript intron_variant - - - - - - rs7257360 19:3667461 C 23396 NM_012398.2 Transcript intron_variant - - - - - - rs7257360 19:3667461 C CCDS56074.1 CCDS56074.1 Transcript intron_variant - - - - - - rs56822749 19:3678077 G CCDS32872.1 CCDS32872.1 Transcript intron_variant - - - - - - rs56822749 19:3678077 G ENSESTG00000018760 ENSESTT00000047461 Transcript intron_variant - - - - - - rs56822749 19:3678077 G ENSESTG00000018760 ENSESTT00000047468 Transcript intron_variant - - - - - - rs56822749 19:3678077 G 23396 NM_001195733.1 Transcript intron_variant - - - - - - rs56822749 19:3678077 G ENSESTG00000018760 ENSESTT00000047475 Transcript intron_variant - - - - - - rs56822749 19:3678077 G 23396 NM_012398.2 Transcript intron_variant - - - - - - rs56822749 19:3678077 G CCDS56074.1 CCDS56074.1 Transcript intron_variant - - - - - - rs6510805 19:4343035 G - ENSR00000214277 RegulatoryFeature regulatory_region_variant - - - - - - rs6510805 19:4343035 G CCDS45926.1 CCDS45926.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4285 rs6510805 19:4343035 G 55620 NM_017720.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4188 rs6510805 19:4343035 G ENSESTG00000013938 ENSESTT00000034859 Transcript upstream_gene_variant - - - - - - DISTANCE=489 rs6510805 19:4343035 G CCDS12128.1 CCDS12128.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4285 rs6510805 19:4343035 G ENSESTG00000014310 ENSESTT00000035874 Transcript upstream_gene_variant - - - - - - DISTANCE=4206 rs6510805 19:4343035 G CCDS54200.1 CCDS54200.1 Transcript upstream_gene_variant - - - - - - DISTANCE=556 rs6510805 19:4343035 G 55620 NM_001013841.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4188 rs6510805 19:4343035 G ENSESTG00000013938 ENSESTT00000034857 Transcript upstream_gene_variant - - - - - - DISTANCE=489 rs6510805 19:4343035 G 84954 NM_001159846.1 Transcript upstream_gene_variant - - - - - - DISTANCE=489 rs6510805 19:4343035 G 84954 NM_032868.4 Transcript upstream_gene_variant - - - - - - DISTANCE=489 rs6510805 19:4343035 G CCDS42470.1 CCDS42470.1 Transcript upstream_gene_variant - - - - - - DISTANCE=556 rs2620839 19:5132051 A - ENSR00000342426 RegulatoryFeature regulatory_region_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013947 Transcript intron_variant - - - - - - rs2620839 19:5132051 A 23030 NM_015015.2 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013949 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013958 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013923 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013926 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013984 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013990 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013972 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000014017 Transcript upstream_gene_variant - - - - - - DISTANCE=1839 rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013981 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013987 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013966 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000013960 Transcript intron_variant - - - - - - rs2620839 19:5132051 A ENSESTG00000005456 ENSESTT00000014013 Transcript upstream_gene_variant - - - - - - DISTANCE=1839 rs2620839 19:5132051 A CCDS12138.1 CCDS12138.1 Transcript intron_variant - - - - - - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013947 Transcript missense_variant 2270 2128 710 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs2620836 19:5135392 G 23030 NM_015015.2 Transcript missense_variant 2354 2128 710 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000014021 Transcript upstream_gene_variant - - - - - - DISTANCE=2579 rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013949 Transcript missense_variant 2270 2128 710 K/E Aag/Gag - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013958 Transcript missense_variant 2343 2128 710 K/E Aag/Gag - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013923 Transcript missense_variant 2270 2128 710 K/E Aag/Gag - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013926 Transcript missense_variant 2270 2128 710 K/E Aag/Gag - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013984 Transcript missense_variant 1839 1651 551 K/E Aag/Gag - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013990 Transcript missense_variant 1839 1651 551 K/E Aag/Gag - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013972 Transcript missense_variant 2343 2128 710 K/E Aag/Gag - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000014017 Transcript 5_prime_UTR_variant 226 - - - - - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013981 Transcript missense_variant 1839 1651 551 K/E Aag/Gag - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013987 Transcript missense_variant 1839 1651 551 K/E Aag/Gag - rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013966 Transcript missense_variant 2343 2128 710 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000013960 Transcript missense_variant 2343 2128 710 K/E Aag/Gag - rs2620836 19:5135392 G CCDS12138.1 CCDS12138.1 Transcript missense_variant 2128 2128 710 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs2620836 19:5135392 G ENSESTG00000005456 ENSESTT00000014013 Transcript 5_prime_UTR_variant 226 - - - - - rs6510841 19:5187668 A - - - intergenic_variant - - - - - - rs758514 19:5272061 G ENSESTG00000006255 ENSESTT00000015794 Transcript intron_variant - - - - - - rs758514 19:5272061 G 5802 NM_002850.3 Transcript intron_variant - - - - - - rs758514 19:5272061 G 5802 NM_130855.2 Transcript intron_variant - - - - - - rs758514 19:5272061 G CCDS12140.1 CCDS12140.1 Transcript intron_variant - - - - - - rs758514 19:5272061 G CCDS12139.1 CCDS12139.1 Transcript intron_variant - - - - - - rs758514 19:5272061 G 5802 NM_130853.2 Transcript intron_variant - - - - - - rs758514 19:5272061 G CCDS45930.1 CCDS45930.1 Transcript intron_variant - - - - - - rs758514 19:5272061 G 5802 NM_130854.2 Transcript intron_variant - - - - - - rs758514 19:5272061 G ENSESTG00000006255 ENSESTT00000015790 Transcript intron_variant - - - - - - rs12980760 19:5369705 C - - - intergenic_variant - - - - - - rs2436533 19:5732986 C 257062 NM_152784.3 Transcript intron_variant - - - - - - rs2436533 19:5732986 C CCDS12149.2 CCDS12149.2 Transcript intron_variant - - - - - - rs2436533 19:5732986 C ENSESTG00000005814 ENSESTT00000014756 Transcript intron_variant - - - - - - rs2436533 19:5732986 C ENSESTG00000005814 ENSESTT00000014753 Transcript intron_variant - - - - - - rs2485269 19:5754718 T 257062 NM_152784.3 Transcript intron_variant - - - - - - rs2485269 19:5754718 T ENSESTG00000005854 ENSESTT00000014840 Transcript upstream_gene_variant - - - - - - DISTANCE=3151 rs2485269 19:5754718 T CCDS12149.2 CCDS12149.2 Transcript intron_variant - - - - - - rs1560695 19:6153427 A ENSESTG00000025451 ENSESTT00000064298 Transcript intron_variant - - - - - - rs1560695 19:6153427 A ENSESTG00000025451 ENSESTT00000064289 Transcript intron_variant - - - - - - rs1560695 19:6153427 A 81616 NM_030924.3 Transcript intron_variant - - - - - - rs1560695 19:6153427 A CCDS12159.1 CCDS12159.1 Transcript intron_variant - - - - - - rs4807839 19:6155421 C ENSESTG00000025451 ENSESTT00000064298 Transcript intron_variant - - - - - - rs4807839 19:6155421 C ENSESTG00000025451 ENSESTT00000064289 Transcript intron_variant - - - - - - rs4807839 19:6155421 C 81616 NM_030924.3 Transcript intron_variant - - - - - - rs4807839 19:6155421 C CCDS12159.1 CCDS12159.1 Transcript intron_variant - - - - - - rs4514808 19:6229800 C 4298 NM_005934.3 Transcript intron_variant - - - - - - rs4514808 19:6229800 C CCDS12160.1 CCDS12160.1 Transcript intron_variant - - - - - - rs4514808 19:6229800 C ENSESTG00000026793 ENSESTT00000067496 Transcript intron_variant - - - - - - rs453462 19:6585921 C ENSESTG00000026493 ENSESTT00000066727 Transcript downstream_gene_variant - - - - - - DISTANCE=4192 rs453462 19:6585921 C CCDS12170.1 CCDS12170.1 Transcript downstream_gene_variant - - - - - - DISTANCE=110 rs453462 19:6585921 C 970 NM_001252.3 Transcript 3_prime_UTR_variant 842 - - - - - rs1963259 19:6985760 G 326342 NR_024075.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8109994 19:6994217 C 326342 NR_024075.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3360 rs6510939 19:6999436 C - - - intergenic_variant - - - - - - rs6510940 19:7003399 C 497049 NR_024372.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1565 rs10416958 19:7207840 G ENSESTG00000031630 ENSESTT00000079868 Transcript intron_variant - - - - - - rs10416958 19:7207840 G CCDS42487.1 CCDS42487.1 Transcript intron_variant - - - - - - rs10416958 19:7207840 G 3643 NM_001079817.1 Transcript intron_variant - - - - - - rs10416958 19:7207840 G CCDS12176.1 CCDS12176.1 Transcript intron_variant - - - - - - rs10416958 19:7207840 G 3643 NM_000208.2 Transcript intron_variant - - - - - - rs11085222 19:7242917 C - ENSR00001417676 RegulatoryFeature regulatory_region_variant - - - - - - rs11085222 19:7242917 C ENSESTG00000031630 ENSESTT00000079868 Transcript intron_variant - - - - - - rs11085222 19:7242917 C CCDS42487.1 CCDS42487.1 Transcript intron_variant - - - - - - rs11085222 19:7242917 C 3643 NM_001079817.1 Transcript intron_variant - - - - - - rs11085222 19:7242917 C CCDS12176.1 CCDS12176.1 Transcript intron_variant - - - - - - rs11085222 19:7242917 C 3643 NM_000208.2 Transcript intron_variant - - - - - - rs10421872 19:7243802 G ENSESTG00000031630 ENSESTT00000079868 Transcript intron_variant - - - - - - rs10421872 19:7243802 G CCDS42487.1 CCDS42487.1 Transcript intron_variant - - - - - - rs10421872 19:7243802 G 3643 NM_001079817.1 Transcript intron_variant - - - - - - rs10421872 19:7243802 G CCDS12176.1 CCDS12176.1 Transcript intron_variant - - - - - - rs10421872 19:7243802 G 3643 NM_000208.2 Transcript intron_variant - - - - - - rs10415183 19:7503965 G 23370 NM_015318.3 Transcript intron_variant - - - - - - rs10415183 19:7503965 G ENSESTG00000030242 ENSESTT00000076491 Transcript intron_variant - - - - - - rs10415183 19:7503965 G ENSESTG00000030242 ENSESTT00000076480 Transcript intron_variant - - - - - - rs10415183 19:7503965 G 23370 NM_001130955.1 Transcript upstream_gene_variant - - - - - - DISTANCE=609 rs10415183 19:7503965 G CCDS45946.1 CCDS45946.1 Transcript upstream_gene_variant - - - - - - DISTANCE=862 rs10415183 19:7503965 G ENSESTG00000030242 ENSESTT00000076457 Transcript intron_variant - - - - - - rs10415183 19:7503965 G ENSESTG00000030242 ENSESTT00000076472 Transcript intron_variant - - - - - - rs10415183 19:7503965 G ENSESTG00000030242 ENSESTT00000076430 Transcript intron_variant - - - - - - rs10415183 19:7503965 G ENSESTG00000030242 ENSESTT00000076486 Transcript intron_variant - - - - - - rs10415183 19:7503965 G CCDS12177.1 CCDS12177.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1336 rs4804637 19:7514901 G 23370 NM_015318.3 Transcript intron_variant - - - - - - rs4804637 19:7514901 G ENSESTG00000030242 ENSESTT00000076491 Transcript intron_variant - - - - - - rs4804637 19:7514901 G ENSESTG00000030242 ENSESTT00000076480 Transcript intron_variant - - - - - - rs4804637 19:7514901 G 23370 NM_001130955.1 Transcript intron_variant - - - - - - rs4804637 19:7514901 G CCDS45946.1 CCDS45946.1 Transcript intron_variant - - - - - - rs4804637 19:7514901 G ENSESTG00000030242 ENSESTT00000076457 Transcript intron_variant - - - - - - rs4804637 19:7514901 G ENSESTG00000030242 ENSESTT00000076472 Transcript intron_variant - - - - - - rs4804637 19:7514901 G ENSESTG00000030242 ENSESTT00000076430 Transcript intron_variant - - - - - - rs4804637 19:7514901 G ENSESTG00000030242 ENSESTT00000076486 Transcript intron_variant - - - - - - rs4804637 19:7514901 G CCDS12177.1 CCDS12177.1 Transcript intron_variant - - - - - - rs502723 19:7848275 T 440508 NR_002931.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4095 rs502723 19:7848275 T ENSESTG00000031418 ENSESTT00000079341 Transcript upstream_gene_variant - - - - - - DISTANCE=4123 rs502723 19:7848275 T ENSESTG00000031418 ENSESTT00000079322 Transcript upstream_gene_variant - - - - - - DISTANCE=4089 rs502723 19:7848275 T ENSESTG00000031418 ENSESTT00000079306 Transcript upstream_gene_variant - - - - - - DISTANCE=4082 rs502723 19:7848275 T ENSESTG00000031418 ENSESTT00000079289 Transcript upstream_gene_variant - - - - - - DISTANCE=4059 rs502723 19:7848275 T ENSESTG00000031418 ENSESTT00000079351 Transcript upstream_gene_variant - - - - - - DISTANCE=4157 rs575935 19:7907474 G - ENSR00000640913 RegulatoryFeature regulatory_region_variant - - - - - - rs575935 19:7907474 G ENSESTG00000033124 ENSESTT00000083695 Transcript intron_variant - - - - - - rs575935 19:7907474 G 115704 NM_001159944.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3912 rs575935 19:7907474 G ENSESTG00000033124 ENSESTT00000083732 Transcript intron_variant - - - - - - rs575935 19:7907474 G 115704 NM_145245.3 Transcript intron_variant - - - - - - rs575935 19:7907474 G ENSESTG00000033124 ENSESTT00000083744 Transcript intron_variant - - - - - - rs575935 19:7907474 G ENSESTG00000033124 ENSESTT00000083736 Transcript intron_variant - - - - - - rs575935 19:7907474 G CCDS12188.1 CCDS12188.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3955 rs575935 19:7907474 G ENSESTG00000033124 ENSESTT00000083728 Transcript intron_variant - - - - - - rs575935 19:7907474 G ENSESTG00000033124 ENSESTT00000083738 Transcript intron_variant - - - - - - rs575935 19:7907474 G CCDS54209.1 CCDS54209.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3955 rs487089 19:7910218 G ENSESTG00000033124 ENSESTT00000083695 Transcript intron_variant - - - - - - rs487089 19:7910218 G 115704 NM_001159944.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1168 rs487089 19:7910218 G ENSESTG00000033124 ENSESTT00000083732 Transcript intron_variant - - - - - - rs487089 19:7910218 G 115704 NM_145245.3 Transcript intron_variant - - - - - - rs487089 19:7910218 G ENSESTG00000033124 ENSESTT00000083744 Transcript intron_variant - - - - - - rs487089 19:7910218 G ENSESTG00000033124 ENSESTT00000083736 Transcript intron_variant - - - - - - rs487089 19:7910218 G ENSESTG00000033124 ENSESTT00000083753 Transcript upstream_gene_variant - - - - - - DISTANCE=3585 rs487089 19:7910218 G CCDS12188.1 CCDS12188.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1211 rs487089 19:7910218 G ENSESTG00000033124 ENSESTT00000083728 Transcript intron_variant - - - - - - rs487089 19:7910218 G ENSESTG00000033124 ENSESTT00000083757 Transcript upstream_gene_variant - - - - - - DISTANCE=3585 rs487089 19:7910218 G ENSESTG00000033124 ENSESTT00000083738 Transcript intron_variant - - - - - - rs487089 19:7910218 G CCDS54209.1 CCDS54209.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1211 rs10410459 19:7928462 C - ENSR00000342928 RegulatoryFeature regulatory_region_variant - - - - - - rs10410459 19:7928462 C ENSESTG00000033124 ENSESTT00000083794 Transcript synonymous_variant 1118 819 273 Y taT/taC - rs10410459 19:7928462 C ENSESTG00000033124 ENSESTT00000083695 Transcript downstream_gene_variant - - - - - - DISTANCE=17 rs10410459 19:7928462 C CCDS12188.1 CCDS12188.1 Transcript synonymous_variant 2259 2259 753 Y taT/taC - rs10410459 19:7928462 C ENSESTG00000033124 ENSESTT00000083765 Transcript downstream_gene_variant - - - - - - DISTANCE=1570 rs10410459 19:7928462 C 115704 NM_001159944.1 Transcript synonymous_variant 2335 2292 764 Y taT/taC - rs10410459 19:7928462 C CCDS54209.1 CCDS54209.1 Transcript synonymous_variant 2292 2292 764 Y taT/taC - rs10410459 19:7928462 C 115704 NM_145245.3 Transcript synonymous_variant 2413 2259 753 Y taT/taC - rs4804246 19:8044987 A CCDS12193.1 CCDS12193.1 Transcript intron_variant - - - - - - rs4804246 19:8044987 A ENSESTG00000033665 ENSESTT00000085137 Transcript intron_variant - - - - - - rs4804246 19:8044987 A 1994 NM_001419.2 Transcript intron_variant - - - - - - rs4804246 19:8044987 A ENSESTG00000033665 ENSESTT00000085111 Transcript intron_variant - - - - - - rs10419743 19:8239610 C - ENSR00000342977 RegulatoryFeature regulatory_region_variant - - - - - - rs10419743 19:8239610 C - - - intergenic_variant - - - - - - rs1820098 19:8936959 T ENSESTG00000030024 ENSESTT00000075617 Transcript upstream_gene_variant - - - - - - DISTANCE=4220 rs1820098 19:8936959 T CCDS12208.1 CCDS12208.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3624 rs1820098 19:8936959 T 148156 NM_144693.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3394 rs1820098 19:8936959 T ENSESTG00000029048 ENSESTT00000073144 Transcript downstream_gene_variant - - - - - - DISTANCE=2173 rs1820098 19:8936959 T ENSESTG00000030024 ENSESTT00000075590 Transcript upstream_gene_variant - - - - - - DISTANCE=3394 rs57902801 19:8998532 C CCDS54212.1 CCDS54212.1 Transcript intron_variant - - - - - - rs57902801 19:8998532 C ENSESTG00000029854 ENSESTT00000075312 Transcript intron_variant - - - - - - rs57902801 19:8998532 C ENSESTG00000029854 ENSESTT00000075255 Transcript intron_variant - - - - - - rs57902801 19:8998532 C 94025 NM_024690.2 Transcript intron_variant - - - - - - rs57902801 19:8998532 C ENSESTG00000029854 ENSESTT00000075296 Transcript intron_variant - - - - - - rs57902801 19:8998532 C ENSESTG00000029854 ENSESTT00000075277 Transcript intron_variant - - - - - - rs7254856 19:9649743 A - ENSR00000214777 RegulatoryFeature regulatory_region_variant - - - - - - rs7254856 19:9649743 A ENSESTG00000029510 ENSESTT00000074498 Transcript upstream_gene_variant - - - - - - DISTANCE=679 rs7254856 19:9649743 A CCDS12215.1 CCDS12215.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2835 rs7254856 19:9649743 A ENSESTG00000029510 ENSESTT00000074396 Transcript upstream_gene_variant - - - - - - DISTANCE=422 rs7254856 19:9649743 A ENSESTG00000029510 ENSESTT00000074510 Transcript upstream_gene_variant - - - - - - DISTANCE=2498 rs7254856 19:9649743 A 79088 NM_024106.1 Transcript upstream_gene_variant - - - - - - DISTANCE=440 rs4804456 19:9844668 A - - - intergenic_variant - - - - - - rs1212202 19:9844773 A - - - intergenic_variant - - - - - - rs6511693 19:10452583 C ENSESTG00000002046 ENSESTT00000005087 Transcript upstream_gene_variant - - - - - - DISTANCE=2239 rs6511693 19:10452583 C 3385 NM_002162.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2238 rs6511693 19:10452583 C CCDS12235.1 CCDS12235.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2293 rs6511693 19:10452583 C ENSESTG00000002046 ENSESTT00000005091 Transcript upstream_gene_variant - - - - - - DISTANCE=2283 rs1861633 19:10974322 G - ENSR00001417866 RegulatoryFeature regulatory_region_variant - - - - - - rs1861633 19:10974322 G CCDS45970.1 CCDS45970.1 Transcript intron_variant - - - - - - rs1861633 19:10974322 G 255809 NM_001136482.1 Transcript intron_variant - - - - - - rs1861633 19:10974322 G ENSESTG00000002408 ENSESTT00000005987 Transcript downstream_gene_variant - - - - - - DISTANCE=3615 rs1861633 19:10974322 G ENSESTG00000002408 ENSESTT00000005996 Transcript intron_variant - - - - - - rs1861633 19:10974322 G ENSESTG00000002408 ENSESTT00000005991 Transcript intron_variant - - - - - - rs4804559 19:11109642 A CCDS45972.1 CCDS45972.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A 6597 NM_001128847.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A CCDS54218.1 CCDS54218.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A 6597 NM_001128845.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A CCDS12253.1 CCDS12253.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006371 Transcript intron_variant - - - - - - rs4804559 19:11109642 A 6597 NM_001128849.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006384 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006395 Transcript intron_variant - - - - - - rs4804559 19:11109642 A 6597 NM_001128848.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A CCDS45973.1 CCDS45973.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006389 Transcript intron_variant - - - - - - rs4804559 19:11109642 A 6597 NM_003072.3 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006339 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006356 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006382 Transcript intron_variant - - - - - - rs4804559 19:11109642 A 6597 NM_001128844.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A CCDS54217.1 CCDS54217.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006381 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006346 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006336 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006387 Transcript intron_variant - - - - - - rs4804559 19:11109642 A 6597 NM_001128846.1 Transcript intron_variant - - - - - - rs4804559 19:11109642 A ENSESTG00000002487 ENSESTT00000006362 Transcript intron_variant - - - - - - rs2738442 19:11221454 C - ENSR00000343450 RegulatoryFeature regulatory_region_variant - - - - - - rs2738442 19:11221454 C 3949 NM_001195800.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C 3949 NM_000527.4 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C 3949 NM_001195802.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C 3949 NM_001195798.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C CCDS58651.1 CCDS58651.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C CCDS58650.1 CCDS58650.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C ENSESTG00000002618 ENSESTT00000006577 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C CCDS56083.1 CCDS56083.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C 3949 NM_001195799.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C 3949 NM_001195803.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C CCDS56085.1 CCDS56085.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C CCDS56084.1 CCDS56084.1 Transcript splice_region_variant,intron_variant - - - - - - rs2738442 19:11221454 C CCDS12254.1 CCDS12254.1 Transcript splice_region_variant,intron_variant - - - - - - rs2605116 19:11576315 C CCDS45978.1 CCDS45978.1 Transcript intron_variant - - - - - - rs2605116 19:11576315 C ENSESTG00000002953 ENSESTT00000007337 Transcript downstream_gene_variant - - - - - - DISTANCE=686 rs2605116 19:11576315 C 1995 NM_032281.2 Transcript intron_variant - - - - - - rs2605116 19:11576315 C 1995 NM_001420.3 Transcript intron_variant - - - - - - rs2605116 19:11576315 C CCDS32912.1 CCDS32912.1 Transcript intron_variant - - - - - - rs2605116 19:11576315 C ENSESTG00000002812 ENSESTT00000006971 Transcript intron_variant - - - - - - rs1269465 19:11956098 C ENSESTG00000012273 ENSESTT00000030801 Transcript upstream_gene_variant - - - - - - DISTANCE=3487 rs1269465 19:11956098 C ENSESTG00000012273 ENSESTT00000030797 Transcript upstream_gene_variant - - - - - - DISTANCE=3464 rs1269465 19:11956098 C ENSESTG00000012273 ENSESTT00000030795 Transcript upstream_gene_variant - - - - - - DISTANCE=3443 rs279168 19:12132168 C ENSESTG00000009352 ENSESTT00000023449 Transcript intron_variant - - - - - - rs279168 19:12132168 C ENSESTG00000012325 ENSESTT00000030916 Transcript intron_variant - - - - - - rs279168 19:12132168 C ENSESTG00000009352 ENSESTT00000023466 Transcript intron_variant - - - - - - rs279168 19:12132168 C 163059 NM_001080411.1 Transcript intron_variant - - - - - - rs279168 19:12132168 C ENSESTG00000009352 ENSESTT00000023461 Transcript intron_variant - - - - - - rs279168 19:12132168 C CCDS45983.1 CCDS45983.1 Transcript intron_variant - - - - - - rs279168 19:12132168 C ENSESTG00000012325 ENSESTT00000030936 Transcript intron_variant - - - - - - rs279168 19:12132168 C ENSESTG00000009352 ENSESTT00000023440 Transcript intron_variant - - - - - - rs279168 19:12132168 C ENSESTG00000009352 ENSESTT00000023457 Transcript intron_variant - - - - - - rs4804176 19:12157334 G ENSESTG00000012325 ENSESTT00000030936 Transcript downstream_gene_variant - - - - - - DISTANCE=245 rs4804176 19:12157334 G 729747 NM_001080404.2 Transcript intron_variant - - - - - - rs4804176 19:12157334 G ENSESTG00000009352 ENSESTT00000023440 Transcript intron_variant - - - - - - rs4804176 19:12157334 G CCDS45984.2 CCDS45984.2 Transcript intron_variant - - - - - - rs4804176 19:12157334 G ENSESTG00000009352 ENSESTT00000023443 Transcript intron_variant - - - - - - rs4804176 19:12157334 G ENSESTG00000012325 ENSESTT00000030940 Transcript downstream_gene_variant - - - - - - DISTANCE=245 rs169200 19:12292329 C ENSESTG00000012355 ENSESTT00000031002 Transcript intron_variant - - - - - - rs169200 19:12292329 C CCDS32916.1 CCDS32916.1 Transcript intron_variant - - - - - - rs169200 19:12292329 C ENSESTG00000012349 ENSESTT00000030988 Transcript intron_variant - - - - - - rs169200 19:12292329 C 7695 NM_003437.3 Transcript intron_variant - - - - - - rs8111612 19:12920127 C 10535 NM_006397.2 Transcript intron_variant - - - - - - rs8111612 19:12920127 C CCDS12282.1 CCDS12282.1 Transcript intron_variant - - - - - - rs8111612 19:12920127 C ENSESTG00000024562 ENSESTT00000062135 Transcript upstream_gene_variant - - - - - - DISTANCE=1005 rs8111612 19:12920127 C ENSESTG00000024489 ENSESTT00000062055 Transcript intron_variant - - - - - - rs10419483 19:13208737 T - ENSR00000215125 RegulatoryFeature regulatory_region_variant - - - - - - rs10419483 19:13208737 T - MA0162.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=1;MOTIF_NAME=Jaspar_Matrix_Egr1:MA0162.1;HIGH_INF_POS=N;MOTIF_SCORE_CHANGE=-0.017 rs10419483 19:13208737 T 4066 NM_005583.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1105 rs10419483 19:13208737 T ENSESTG00000024168 ENSESTT00000061076 Transcript intron_variant - - - - - - rs10419483 19:13208737 T CCDS12292.1 CCDS12292.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1396 rs10419483 19:13208737 T ENSESTG00000025585 ENSESTT00000064527 Transcript downstream_gene_variant - - - - - - DISTANCE=1702 rs10419483 19:13208737 T ENSESTG00000025604 ENSESTT00000064567 Transcript intron_variant - - - - - - rs10419483 19:13208737 T ENSESTG00000024168 ENSESTT00000061460 Transcript downstream_gene_variant - - - - - - DISTANCE=973 rs10419483 19:13208737 T ENSESTG00000024168 ENSESTT00000061475 Transcript intron_variant - - - - - - rs10419483 19:13208737 T ENSESTG00000025585 ENSESTT00000064510 Transcript downstream_gene_variant - - - - - - DISTANCE=1608 rs10419483 19:13208737 T ENSESTG00000024168 ENSESTT00000061211 Transcript downstream_gene_variant - - - - - - DISTANCE=3163 rs10419483 19:13208737 T 4784 NM_002501.2 Transcript 3_prime_UTR_variant 4703 - - - - - rs10419483 19:13208737 T ENSESTG00000024168 ENSESTT00000061426 Transcript downstream_gene_variant - - - - - - DISTANCE=1721 rs10419483 19:13208737 T ENSESTG00000025604 ENSESTT00000064548 Transcript intron_variant - - - - - - rs10419483 19:13208737 T ENSESTG00000024168 ENSESTT00000061402 Transcript downstream_gene_variant - - - - - - DISTANCE=1721 rs10419483 19:13208737 T ENSESTG00000024168 ENSESTT00000061231 Transcript intron_variant - - - - - - rs10419483 19:13208737 T ENSESTG00000024168 ENSESTT00000061442 Transcript downstream_gene_variant - - - - - - DISTANCE=1721 rs8106876 19:13290830 G - - - intergenic_variant - - - - - - rs1871470 19:13476394 C CCDS45998.1 CCDS45998.1 Transcript intron_variant - - - - - - rs1871470 19:13476394 C 773 NM_000068.3 Transcript intron_variant - - - - - - rs1871470 19:13476394 C 773 NM_023035.2 Transcript intron_variant - - - - - - rs1871470 19:13476394 C CCDS45999.1 CCDS45999.1 Transcript intron_variant - - - - - - rs1871470 19:13476394 C 773 NM_001174080.1 Transcript intron_variant - - - - - - rs1871470 19:13476394 C 773 NM_001127222.1 Transcript intron_variant - - - - - - rs1871470 19:13476394 C 773 NM_001127221.1 Transcript intron_variant - - - - - - rs346170 19:13842660 C - ENSR00000043167 RegulatoryFeature regulatory_region_variant - - - - - - rs346170 19:13842660 C - - - intergenic_variant - - - - - - rs7259525 19:13955993 G 100996314 XM_003846295.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4650 rs6511972 19:14895025 G - - - intergenic_variant - - - - - - rs4808663 19:15009340 T - - - intergenic_variant - - - - - - rs2886741 19:15184548 G - ENSR00000344054 RegulatoryFeature regulatory_region_variant - - - - - - rs2886741 19:15184548 G - - - intergenic_variant - - - - - - rs2058322 19:15508362 C ENSESTG00000030013 ENSESTT00000075716 Transcript downstream_gene_variant - - - - - - DISTANCE=3278 rs2058322 19:15508362 C ENSESTG00000030013 ENSESTT00000075677 Transcript downstream_gene_variant - - - - - - DISTANCE=3379 rs2058322 19:15508362 C ENSESTG00000016220 ENSESTT00000040774 Transcript missense_variant 379 165 55 H/Q caC/caG - rs2058322 19:15508362 C CCDS46005.1 CCDS46005.1 Transcript missense_variant 1374 1374 458 H/Q caC/caG - PolyPhen=benign;SIFT=tolerated rs2058322 19:15508362 C 26993 NM_014371.2 Transcript missense_variant 1473 1374 458 H/Q caC/caG - PolyPhen=benign;SIFT=tolerated rs2058322 19:15508362 C ENSESTG00000016220 ENSESTT00000040763 Transcript missense_variant 324 228 76 H/Q caC/caG - rs2058322 19:15508362 C ENSESTG00000030013 ENSESTT00000075734 Transcript downstream_gene_variant - - - - - - DISTANCE=3417 rs2058322 19:15508362 C ENSESTG00000016220 ENSESTT00000040778 Transcript missense_variant 349 165 55 H/Q caC/caG - rs10854144 19:15512931 A ENSESTG00000030013 ENSESTT00000075716 Transcript intron_variant - - - - - - rs10854144 19:15512931 A ENSESTG00000030013 ENSESTT00000075677 Transcript intron_variant - - - - - - rs10854144 19:15512931 A ENSESTG00000030013 ENSESTT00000075556 Transcript downstream_gene_variant - - - - - - DISTANCE=1517 rs10854144 19:15512931 A ENSESTG00000016220 ENSESTT00000040774 Transcript upstream_gene_variant - - - - - - DISTANCE=2794 rs10854144 19:15512931 A CCDS46005.1 CCDS46005.1 Transcript intron_variant - - - - - - rs10854144 19:15512931 A 26993 NM_014371.2 Transcript intron_variant - - - - - - rs10854144 19:15512931 A ENSESTG00000016220 ENSESTT00000040763 Transcript upstream_gene_variant - - - - - - DISTANCE=2712 rs10854144 19:15512931 A ENSESTG00000030013 ENSESTT00000075734 Transcript intron_variant - - - - - - rs10854144 19:15512931 A ENSESTG00000016220 ENSESTT00000040778 Transcript upstream_gene_variant - - - - - - DISTANCE=3359 rs1153001 19:15683091 G ENSESTG00000029823 ENSESTT00000075004 Transcript intron_variant - - - - - - rs1153001 19:15683091 G ENSESTG00000029817 ENSESTT00000074989 Transcript intron_variant - - - - - - rs4808412 19:16038518 G 57834 NM_001128932.1 Transcript intron_variant - - - - - - rs4808412 19:16038518 G CCDS12337.1 CCDS12337.1 Transcript intron_variant - - - - - - rs4808412 19:16038518 G ENSESTG00000010186 ENSESTT00000025468 Transcript intron_variant - - - - - - rs4808412 19:16038518 G 57834 NM_021187.3 Transcript intron_variant - - - - - - rs4808412 19:16038518 G ENSESTG00000010186 ENSESTT00000025480 Transcript intron_variant - - - - - - rs4808412 19:16038518 G ENSESTG00000010165 ENSESTT00000025441 Transcript intron_variant - - - - - - rs492281 19:16303464 G ENSESTG00000009866 ENSESTT00000024721 Transcript downstream_gene_variant - - - - - - DISTANCE=614 rs492281 19:16303464 G CCDS12341.1 CCDS12341.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1698 rs492281 19:16303464 G 26017 NM_014077.2 Transcript downstream_gene_variant - - - - - - DISTANCE=607 rs8099915 19:16303845 G CCDS12341.1 CCDS12341.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2079 rs8099915 19:16303845 G 8907 NM_001130524.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4820 rs8099915 19:16303845 G 8907 NM_032493.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4820 rs8099915 19:16303845 G 26017 NM_014077.2 Transcript downstream_gene_variant - - - - - - DISTANCE=988 rs8099915 19:16303845 G ENSESTG00000009866 ENSESTT00000024721 Transcript downstream_gene_variant - - - - - - DISTANCE=995 rs8099915 19:16303845 G ENSESTG00000009886 ENSESTT00000024799 Transcript upstream_gene_variant - - - - - - DISTANCE=4877 rs8099915 19:16303845 G CCDS46008.1 CCDS46008.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4993 rs8099915 19:16303845 G CCDS12342.1 CCDS12342.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4993 rs6512093 19:16363375 G - - - intergenic_variant - - - - - - rs10412239 19:16446235 G - - - intergenic_variant - - - - - - rs8102735 19:16501289 A ENSESTG00000010094 ENSESTT00000025382 Transcript intron_variant - - - - - - rs8102735 19:16501289 A 58513 NR_047665.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8102735 19:16501289 A ENSESTG00000010094 ENSESTT00000025363 Transcript intron_variant - - - - - - rs8102735 19:16501289 A CCDS32944.1 CCDS32944.1 Transcript intron_variant - - - - - - rs8102735 19:16501289 A ENSESTG00000010094 ENSESTT00000025367 Transcript intron_variant - - - - - - rs8102735 19:16501289 A CCDS58653.1 CCDS58653.1 Transcript intron_variant - - - - - - rs8102735 19:16501289 A CCDS58654.1 CCDS58654.1 Transcript intron_variant - - - - - - rs8102735 19:16501289 A 58513 NR_047666.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8102735 19:16501289 A ENSESTG00000010094 ENSESTT00000025343 Transcript intron_variant - - - - - - rs8102735 19:16501289 A ENSESTG00000010094 ENSESTT00000025350 Transcript intron_variant - - - - - - rs8102735 19:16501289 A ENSESTG00000010094 ENSESTT00000025377 Transcript intron_variant - - - - - - rs8102735 19:16501289 A 58513 NM_001258374.1 Transcript intron_variant - - - - - - rs8102735 19:16501289 A ENSESTG00000010094 ENSESTT00000025358 Transcript intron_variant - - - - - - rs8102735 19:16501289 A 58513 NM_001258375.1 Transcript intron_variant - - - - - - rs8102735 19:16501289 A 58513 NM_021235.2 Transcript intron_variant - - - - - - rs8102735 19:16501289 A ENSESTG00000010094 ENSESTT00000025360 Transcript intron_variant - - - - - - rs773854 19:17020249 G 27151 NM_015692.2 Transcript intron_variant - - - - - - rs773854 19:17020249 G CCDS42519.1 CCDS42519.1 Transcript intron_variant - - - - - - rs773854 19:17020249 G ENSESTG00000028976 ENSESTT00000073052 Transcript intron_variant - - - - - - rs10417590 19:17054854 G 27151 NM_015692.2 Transcript intron_variant - - - - - - rs10417590 19:17054854 G CCDS42519.1 CCDS42519.1 Transcript intron_variant - - - - - - rs10417590 19:17054854 G ENSESTG00000028947 ENSESTT00000072862 Transcript downstream_gene_variant - - - - - - DISTANCE=3038 rs8104398 19:17266638 G ENSESTG00000027439 ENSESTT00000069499 Transcript intron_variant - - - - - - rs8104398 19:17266638 G ENSESTG00000027439 ENSESTT00000069489 Transcript intron_variant - - - - - - rs8104398 19:17266638 G 4650 NM_004145.3 Transcript intron_variant - - - - - - rs8104398 19:17266638 G ENSESTG00000027439 ENSESTT00000069444 Transcript intron_variant - - - - - - rs8104398 19:17266638 G ENSESTG00000027439 ENSESTT00000069113 Transcript intron_variant - - - - - - rs8104398 19:17266638 G ENSESTG00000027727 ENSESTT00000069769 Transcript upstream_gene_variant - - - - - - DISTANCE=4246 rs8104398 19:17266638 G ENSESTG00000027439 ENSESTT00000069466 Transcript intron_variant - - - - - - rs8104398 19:17266638 G ENSESTG00000027439 ENSESTT00000069522 Transcript intron_variant - - - - - - rs8104398 19:17266638 G ENSESTG00000027439 ENSESTT00000069129 Transcript downstream_gene_variant - - - - - - DISTANCE=1476 rs8104398 19:17266638 G 4650 NM_001130065.1 Transcript intron_variant - - - - - - rs8104398 19:17266638 G CCDS46010.1 CCDS46010.1 Transcript intron_variant - - - - - - rs4808612 19:17367109 C ENSESTG00000028766 ENSESTT00000072385 Transcript downstream_gene_variant - - - - - - DISTANCE=3358 rs4808612 19:17367109 C CCDS12353.1 CCDS12353.1 Transcript intron_variant - - - - - - rs4808612 19:17367109 C ENSESTG00000028771 ENSESTT00000072490 Transcript intron_variant - - - - - - rs4808612 19:17367109 C ENSESTG00000028771 ENSESTT00000072505 Transcript intron_variant - - - - - - rs4808612 19:17367109 C 83878 NM_031941.3 Transcript intron_variant - - - - - - rs11667687 19:17818312 G - - - intergenic_variant - - - - - - rs265554 19:17898194 T ENSESTG00000009458 ENSESTT00000023804 Transcript intron_variant - - - - - - rs265554 19:17898194 T 23149 NM_001161357.1 Transcript intron_variant - - - - - - rs265554 19:17898194 T CCDS32955.1 CCDS32955.1 Transcript intron_variant - - - - - - rs265554 19:17898194 T ENSESTG00000009458 ENSESTT00000023790 Transcript downstream_gene_variant - - - - - - DISTANCE=754 rs265554 19:17898194 T ENSESTG00000009458 ENSESTT00000023788 Transcript intron_variant - - - - - - rs265554 19:17898194 T 23149 NM_015122.2 Transcript intron_variant - - - - - - rs265554 19:17898194 T ENSESTG00000009458 ENSESTT00000023772 Transcript downstream_gene_variant - - - - - - DISTANCE=754 rs265554 19:17898194 T 23149 NM_001161358.1 Transcript intron_variant - - - - - - rs265554 19:17898194 T 23149 NM_001161359.1 Transcript intron_variant - - - - - - rs265554 19:17898194 T ENSESTG00000009458 ENSESTT00000023765 Transcript intron_variant - - - - - - rs265554 19:17898194 T ENSESTG00000009458 ENSESTT00000023807 Transcript downstream_gene_variant - - - - - - DISTANCE=754 rs1024447 19:18959552 G - ENSR00000344781 RegulatoryFeature regulatory_region_variant - - - - - - rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010822 Transcript intron_variant - - - - - - rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010937 Transcript upstream_gene_variant - - - - - - DISTANCE=423 rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010814 Transcript intron_variant - - - - - - rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010945 Transcript upstream_gene_variant - - - - - - DISTANCE=1079 rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010919 Transcript upstream_gene_variant - - - - - - DISTANCE=265 rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010939 Transcript upstream_gene_variant - - - - - - DISTANCE=423 rs1024447 19:18959552 G CCDS12386.1 CCDS12386.1 Transcript intron_variant - - - - - - rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010929 Transcript upstream_gene_variant - - - - - - DISTANCE=265 rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010934 Transcript upstream_gene_variant - - - - - - DISTANCE=339 rs1024447 19:18959552 G 5976 NM_002911.3 Transcript intron_variant - - - - - - rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010819 Transcript downstream_gene_variant - - - - - - DISTANCE=2620 rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010825 Transcript intron_variant - - - - - - rs1024447 19:18959552 G ENSESTG00000004284 ENSESTT00000010931 Transcript upstream_gene_variant - - - - - - DISTANCE=265 rs10406851 19:19059779 C - ENSR00000344803 RegulatoryFeature regulatory_region_variant - - - - - - rs10406851 19:19059779 C - - - intergenic_variant - - - - - - rs2916077 19:19547086 C 54815 NM_017660.3 Transcript intron_variant - - - - - - rs2916077 19:19547086 C 693225 NR_030370.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1119 rs2916077 19:19547086 C ENSESTG00000000254 ENSESTT00000000652 Transcript intron_variant - - - - - - rs2916077 19:19547086 C ENSESTG00000000254 ENSESTT00000000653 Transcript intron_variant - - - - - - rs4341873 19:20433216 A - - - intergenic_variant - - - - - - rs6511109 19:20639013 C - - - intergenic_variant - - - - - - rs2217345 19:20757200 A - - - intergenic_variant - - - - - - rs4808257 19:20818989 C CCDS42535.1 CCDS42535.1 Transcript intron_variant - - - - - - rs4808257 19:20818989 C 199777 NM_001076675.2 Transcript intron_variant - - - - - - rs279806 19:21465610 T - - - intergenic_variant - - - - - - rs2650756 19:21703367 A ENSESTG00000023242 ENSESTT00000058720 Transcript intron_variant - - - - - - rs2650756 19:21703367 A CCDS42537.1 CCDS42537.1 Transcript intron_variant - - - - - - rs2650756 19:21703367 A 353088 NM_001001415.2 Transcript intron_variant - - - - - - rs2650756 19:21703367 A ENSESTG00000023242 ENSESTT00000058740 Transcript intron_variant - - - - - - rs2650756 19:21703367 A ENSESTG00000023242 ENSESTT00000058708 Transcript intron_variant - - - - - - rs1818700 19:21817018 C - - - intergenic_variant - - - - - - rs10413460 19:21880221 C - - - intergenic_variant - - - - - - rs8107426 19:21889344 G - ENSR00000215889 RegulatoryFeature regulatory_region_variant - - - - - - rs8107426 19:21889344 G - - - intergenic_variant - - - - - - rs4499356 19:21926317 T CCDS42538.1 CCDS42538.1 Transcript intron_variant - - - - - - rs4499356 19:21926317 T 163227 NM_173531.3 Transcript intron_variant - - - - - - rs6511289 19:21936867 T CCDS42538.1 CCDS42538.1 Transcript intron_variant - - - - - - rs6511289 19:21936867 T 163227 NM_173531.3 Transcript intron_variant - - - - - - rs6511289 19:21936867 T 641367 NR_024523.1 Transcript downstream_gene_variant - - - - - - DISTANCE=627 rs4277456 19:21951417 G CCDS42538.1 CCDS42538.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1186 rs4277456 19:21951417 G 163227 NM_173531.3 Transcript upstream_gene_variant - - - - - - DISTANCE=987 rs4809177 19:21951869 C CCDS42538.1 CCDS42538.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1638 rs4809177 19:21951869 C 163227 NM_173531.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1439 rs2435011 19:22085078 C - - - intergenic_variant - - - - - - rs430357 19:22216401 A - - - intergenic_variant - - - - - - rs1036234 19:22279707 C - - - intergenic_variant - - - - - - rs1526887 19:22376259 T 163223 NM_001001411.2 Transcript intron_variant - - - - - - rs1526887 19:22376259 T CCDS42539.1 CCDS42539.1 Transcript intron_variant - - - - - - rs281165 19:22419838 C - - - intergenic_variant - - - - - - rs281167 19:22421006 A - - - intergenic_variant - - - - - - rs2935278 19:22619046 G - - - intergenic_variant - - - - - - rs2569423 19:22682083 G - - - intergenic_variant - - - - - - rs10424349 19:23082167 T - - - intergenic_variant - - - - - - rs2935458 19:23243239 C - - - intergenic_variant - - - - - - rs12984820 19:23632906 T - - - intergenic_variant - - - - - - rs10410652 19:23970851 T 388524 NR_003662.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs10410652 19:23970851 T ENSESTG00000031015 ENSESTT00000078089 Transcript intron_variant - - - - - - rs7248899 19:24044342 G - - - intergenic_variant - - - - - - rs6511656 19:24049464 A - - - intergenic_variant - - - - - - rs1725900 19:24411265 T - - - intergenic_variant - - - - - - rs2115380 19:27854640 C - - - intergenic_variant - - - - - - rs759043 19:28251498 G - - - intergenic_variant - - - - - - rs1975034 19:28642547 G - - - intergenic_variant - - - - - - rs4530281 19:28835621 C ENSESTG00000005921 ENSESTT00000014990 Transcript intron_variant - - - - - - rs8100268 19:28891238 C - - - intergenic_variant - - - - - - rs8113185 19:29488862 A ENSESTG00000005881 ENSESTT00000014914 Transcript upstream_gene_variant - - - - - - DISTANCE=4601 rs8113185 19:29488862 A 100505835 NR_040036.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4600 rs1013425 19:29693453 A 7386 NM_006003.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4714 rs1013425 19:29693453 A ENSESTG00000008003 ENSESTT00000020233 Transcript downstream_gene_variant - - - - - - DISTANCE=4903 rs1019369 19:29790773 G 284395 NR_040029.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7257206 19:29895461 G 284395 NR_040029.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11084025 19:30081863 G - - - intergenic_variant - - - - - - rs2866311 19:30200276 C - ENSR00000641404 RegulatoryFeature regulatory_region_variant - - - - - - rs2866311 19:30200276 C 83636 NR_045690.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2866311 19:30200276 C CCDS12418.2 CCDS12418.2 Transcript upstream_gene_variant - - - - - - DISTANCE=956 rs2866311 19:30200276 C ENSESTG00000007990 ENSESTT00000020177 Transcript intron_variant - - - - - - rs2866311 19:30200276 C ENSESTG00000007990 ENSESTT00000020187 Transcript upstream_gene_variant - - - - - - DISTANCE=729 rs2866311 19:30200276 C 83636 NM_001256047.1 Transcript intron_variant - - - - - - rs2866311 19:30200276 C 83636 NM_031448.4 Transcript intron_variant - - - - - - rs2866311 19:30200276 C ENSESTG00000007990 ENSESTT00000020181 Transcript intron_variant - - - - - - rs2866311 19:30200276 C 83636 NM_001031726.3 Transcript intron_variant - - - - - - rs2866311 19:30200276 C ENSESTG00000007990 ENSESTT00000020166 Transcript intron_variant - - - - - - rs2866311 19:30200276 C 83636 NR_045692.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2866311 19:30200276 C 83636 NR_045691.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2866311 19:30200276 C 83636 NM_001256046.1 Transcript intron_variant - - - - - - rs2866311 19:30200276 C CCDS42542.1 CCDS42542.1 Transcript intron_variant - - - - - - rs277091 19:30551988 C - ENSR00000216048 RegulatoryFeature regulatory_region_variant - - - - - - rs277091 19:30551988 C - - - intergenic_variant - - - - - - rs7258652 19:30703731 G - - - intergenic_variant - - - - - - rs4805570 19:30963121 C CCDS32984.1 CCDS32984.1 Transcript intron_variant - - - - - - rs4805570 19:30963121 C 9745 NM_014717.1 Transcript intron_variant - - - - - - rs4805570 19:30963121 C ENSESTG00000032396 ENSESTT00000081790 Transcript intron_variant - - - - - - rs4805586 19:31088090 C ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs8100216 19:31093090 T ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs10403405 19:31093484 G ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs10409596 19:31093921 G ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs10407125 19:31106391 T ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs2195957 19:31111199 C ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs892097 19:31120752 G ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs4805591 19:31123852 G ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs4804939 19:31134073 C ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs7247574 19:31137414 G ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs892096 19:31137585 C ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs892094 19:31137766 T ENSESTG00000032408 ENSESTT00000081803 Transcript intron_variant - - - - - - rs10414268 19:31329471 A - - - intergenic_variant - - - - - - rs182179 19:31437344 A - - - intergenic_variant - - - - - - rs278175 19:31463048 C - - - intergenic_variant - - - - - - rs4239565 19:31657654 C - - - intergenic_variant - - - - - - rs277429 19:32237373 T - - - intergenic_variant - - - - - - rs4444444 19:33726566 A - ENSR00000141662 RegulatoryFeature regulatory_region_variant - - - - - - rs4444444 19:33726566 A - - - intergenic_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041611 Transcript intron_variant - - - - - - rs10853927 19:33972017 G 5184 NM_001166056.1 Transcript intron_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041658 Transcript intron_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041643 Transcript intron_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041663 Transcript intron_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041682 Transcript upstream_gene_variant - - - - - - DISTANCE=3851 rs10853927 19:33972017 G CCDS42544.1 CCDS42544.1 Transcript intron_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041678 Transcript intron_variant - - - - - - rs10853927 19:33972017 G CCDS54244.1 CCDS54244.1 Transcript intron_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041662 Transcript intron_variant - - - - - - rs10853927 19:33972017 G 5184 NM_001166057.1 Transcript intron_variant - - - - - - rs10853927 19:33972017 G CCDS54245.1 CCDS54245.1 Transcript intron_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041671 Transcript intron_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041596 Transcript intron_variant - - - - - - rs10853927 19:33972017 G ENSESTG00000016515 ENSESTT00000041647 Transcript intron_variant - - - - - - rs10853927 19:33972017 G 5184 NM_000285.3 Transcript intron_variant - - - - - - rs284341 19:34202161 C CCDS12433.1 CCDS12433.1 Transcript intron_variant - - - - - - rs284341 19:34202161 C ENSESTG00000016315 ENSESTT00000040953 Transcript intron_variant - - - - - - rs284341 19:34202161 C 64377 NM_001127896.1 Transcript intron_variant - - - - - - rs284341 19:34202161 C 64377 NM_022467.3 Transcript intron_variant - - - - - - rs284341 19:34202161 C 64377 NM_001127895.1 Transcript intron_variant - - - - - - rs12610688 19:35073575 T 643719 NR_027620.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4979 rs9304857 19:35165758 T ENSESTG00000007895 ENSESTT00000019950 Transcript upstream_gene_variant - - - - - - DISTANCE=2836 rs9304857 19:35165758 T CCDS46042.1 CCDS46042.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3952 rs9304857 19:35165758 T ENSESTG00000007895 ENSESTT00000019965 Transcript upstream_gene_variant - - - - - - DISTANCE=2857 rs9304857 19:35165758 T ENSESTG00000007895 ENSESTT00000019959 Transcript upstream_gene_variant - - - - - - DISTANCE=2850 rs9304857 19:35165758 T 55900 NM_018443.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2809 rs9304857 19:35165758 T 55900 NM_001012320.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2809 rs10418182 19:35183015 C ENSESTG00000007895 ENSESTT00000019950 Transcript intron_variant - - - - - - rs10418182 19:35183015 C ENSESTG00000007895 ENSESTT00000019965 Transcript intron_variant - - - - - - rs10418182 19:35183015 C ENSESTG00000007895 ENSESTT00000019959 Transcript intron_variant - - - - - - rs11668096 19:35186292 G ENSESTG00000007895 ENSESTT00000019950 Transcript intron_variant - - - - - - rs11668096 19:35186292 G ENSESTG00000007895 ENSESTT00000019965 Transcript intron_variant - - - - - - rs11668096 19:35186292 G ENSESTG00000007895 ENSESTT00000019959 Transcript intron_variant - - - - - - rs1673001 19:35582075 G - ENSR00000345828 RegulatoryFeature regulatory_region_variant - - - - - - rs1673001 19:35582075 G 100128675 NR_024562.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1673001 19:35582075 G ENSESTG00000007321 ENSESTT00000018455 Transcript intron_variant - - - - - - rs1673001 19:35582075 G 100128675 NR_024561.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2445823 19:35619399 G ENSESTG00000010595 ENSESTT00000026573 Transcript downstream_gene_variant - - - - - - DISTANCE=4840 rs2445823 19:35619399 G 5349 NM_001136007.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4171 rs2445823 19:35619399 G ENSESTG00000007218 ENSESTT00000018238 Transcript intron_variant - - - - - - rs2445823 19:35619399 G 5349 NM_001136012.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4171 rs2445823 19:35619399 G ENSESTG00000010595 ENSESTT00000026565 Transcript downstream_gene_variant - - - - - - DISTANCE=4840 rs2445823 19:35619399 G ENSESTG00000007218 ENSESTT00000018224 Transcript intron_variant - - - - - - rs2445823 19:35619399 G ENSESTG00000007218 ENSESTT00000018235 Transcript intron_variant - - - - - - rs2445823 19:35619399 G ENSESTG00000007218 ENSESTT00000018205 Transcript downstream_gene_variant - - - - - - DISTANCE=2825 rs2445823 19:35619399 G ENSESTG00000010595 ENSESTT00000026574 Transcript downstream_gene_variant - - - - - - DISTANCE=4840 rs2445823 19:35619399 G CCDS12444.1 CCDS12444.1 Transcript intron_variant - - - - - - rs2445823 19:35619399 G ENSESTG00000007218 ENSESTT00000018226 Transcript intron_variant - - - - - - rs2445823 19:35619399 G 5349 NM_001136011.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4171 rs2445823 19:35619399 G ENSESTG00000007218 ENSESTT00000018231 Transcript downstream_gene_variant - - - - - - DISTANCE=3037 rs2445823 19:35619399 G 163175 NM_139284.2 Transcript intron_variant - - - - - - rs2445823 19:35619399 G 5349 NM_021910.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4171 rs2445823 19:35619399 G 5349 NM_005971.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4171 rs551993 19:35732962 A - - - intergenic_variant - - - - - - rs2141958 19:35777076 T CCDS12454.1 CCDS12454.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1131 rs2141958 19:35777076 T ENSESTG00000010754 ENSESTT00000026913 Transcript downstream_gene_variant - - - - - - DISTANCE=1033 rs2141958 19:35777076 T 57817 NM_021175.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1030 rs2141958 19:35777076 T ENSESTG00000010754 ENSESTT00000026911 Transcript downstream_gene_variant - - - - - - DISTANCE=1033 rs4805121 19:35838135 G - ENSR00000345887 RegulatoryFeature regulatory_region_variant - - - - - - rs4805121 19:35838135 G 933 NM_001185099.1 Transcript 3_prime_UTR_variant 2899 - - - - - rs4805121 19:35838135 G 2864 NM_005303.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4310 rs4805121 19:35838135 G ENSESTG00000010793 ENSESTT00000027103 Transcript 3_prime_UTR_variant 3233 - - - - - rs4805121 19:35838135 G CCDS54247.1 CCDS54247.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1034 rs4805121 19:35838135 G 933 NM_001771.3 Transcript 3_prime_UTR_variant 3163 - - - - - rs4805121 19:35838135 G CCDS54249.1 CCDS54249.1 Transcript downstream_gene_variant - - - - - - DISTANCE=535 rs4805121 19:35838135 G CCDS54248.1 CCDS54248.1 Transcript downstream_gene_variant - - - - - - DISTANCE=535 rs4805121 19:35838135 G ENSESTG00000010793 ENSESTT00000027097 Transcript 3_prime_UTR_variant 3002 - - - - - rs4805121 19:35838135 G CCDS12458.1 CCDS12458.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4320 rs4805121 19:35838135 G 100847070 NR_049828.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1605 rs4805121 19:35838135 G 933 NM_001185101.1 Transcript 3_prime_UTR_variant 2632 - - - - - rs4805121 19:35838135 G 933 NM_001185100.1 Transcript 3_prime_UTR_variant 3044 - - - - - rs4805121 19:35838135 G CCDS12457.1 CCDS12457.1 Transcript downstream_gene_variant - - - - - - DISTANCE=535 rs4805121 19:35838135 G ENSESTG00000010793 ENSESTT00000027115 Transcript downstream_gene_variant - - - - - - DISTANCE=1808 rs231590 19:36225281 G ENSESTG00000011026 ENSESTT00000027684 Transcript upstream_gene_variant - - - - - - DISTANCE=2573 rs231590 19:36225281 G CCDS12472.1 CCDS12472.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4900 rs231590 19:36225281 G ENSESTG00000011026 ENSESTT00000027659 Transcript intron_variant - - - - - - rs231590 19:36225281 G ENSESTG00000011017 ENSESTT00000027643 Transcript downstream_gene_variant - - - - - - DISTANCE=1853 rs231590 19:36225281 G ENSESTG00000006778 ENSESTT00000017239 Transcript downstream_gene_variant - - - - - - DISTANCE=4944 rs231590 19:36225281 G ENSESTG00000006855 ENSESTT00000017426 Transcript intron_variant - - - - - - rs231590 19:36225281 G ENSESTG00000011026 ENSESTT00000027668 Transcript intron_variant - - - - - - rs231590 19:36225281 G 79713 NM_024660.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4870 rs231590 19:36225281 G ENSESTG00000006778 ENSESTT00000017265 Transcript downstream_gene_variant - - - - - - DISTANCE=4872 rs231590 19:36225281 G ENSESTG00000006778 ENSESTT00000017260 Transcript downstream_gene_variant - - - - - - DISTANCE=4763 rs231590 19:36225281 G ENSESTG00000006778 ENSESTT00000017251 Transcript downstream_gene_variant - - - - - - DISTANCE=4835 rs231590 19:36225281 G 9757 NM_014727.1 Transcript intron_variant - - - - - - rs231590 19:36225281 G CCDS46055.1 CCDS46055.1 Transcript intron_variant - - - - - - rs231590 19:36225281 G ENSESTG00000011026 ENSESTT00000027685 Transcript upstream_gene_variant - - - - - - DISTANCE=3343 rs170758 19:36243089 C ENSESTG00000011061 ENSESTT00000027782 Transcript upstream_gene_variant - - - - - - DISTANCE=1652 rs170758 19:36243089 C ENSESTG00000011061 ENSESTT00000027760 Transcript missense_variant 182 47 16 V/A gTc/gCc - PolyPhen=benign rs170758 19:36243089 C ENSESTG00000011445 ENSESTT00000028745 Transcript downstream_gene_variant - - - - - - DISTANCE=3441 rs170758 19:36243089 C ENSESTG00000011061 ENSESTT00000027746 Transcript 5_prime_UTR_variant 213 - - - - - rs170758 19:36243089 C ENSESTG00000011042 ENSESTT00000027705 Transcript downstream_gene_variant - - - - - - DISTANCE=4678 rs170758 19:36243089 C ENSESTG00000011061 ENSESTT00000027749 Transcript downstream_gene_variant - - - - - - DISTANCE=16 rs170758 19:36243089 C 126393 NM_144617.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2378 rs170758 19:36243089 C CCDS12475.1 CCDS12475.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3334 rs170758 19:36243089 C ENSESTG00000011076 ENSESTT00000027794 Transcript upstream_gene_variant - - - - - - DISTANCE=2381 rs170758 19:36243089 C ENSESTG00000011061 ENSESTT00000027778 Transcript missense_variant 239 5 2 V/A gTc/gCc - rs170758 19:36243089 C 55957 NM_019104.2 Transcript missense_variant 411 47 16 V/A gTc/gCc - PolyPhen=benign;SIFT=tolerated rs170758 19:36243089 C ENSESTG00000011477 ENSESTT00000028793 Transcript upstream_gene_variant - - - - - - DISTANCE=3936 rs170758 19:36243089 C ENSESTG00000011061 ENSESTT00000027756 Transcript missense_variant 198 47 16 V/A gTc/gCc - PolyPhen=benign;SIFT=tolerated rs231243 19:36243813 A ENSESTG00000011061 ENSESTT00000027782 Transcript upstream_gene_variant - - - - - - DISTANCE=928 rs231243 19:36243813 A ENSESTG00000011061 ENSESTT00000027760 Transcript downstream_gene_variant - - - - - - DISTANCE=141 rs231243 19:36243813 A ENSESTG00000011445 ENSESTT00000028745 Transcript downstream_gene_variant - - - - - - DISTANCE=2717 rs231243 19:36243813 A ENSESTG00000011061 ENSESTT00000027746 Transcript splice_acceptor_variant - - - - - - rs231243 19:36243813 A ENSESTG00000011061 ENSESTT00000027749 Transcript downstream_gene_variant - - - - - - DISTANCE=740 rs231243 19:36243813 A 126393 NM_144617.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1654 rs231243 19:36243813 A CCDS12475.1 CCDS12475.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2610 rs231243 19:36243813 A ENSESTG00000011076 ENSESTT00000027794 Transcript upstream_gene_variant - - - - - - DISTANCE=1657 rs231243 19:36243813 A ENSESTG00000011061 ENSESTT00000027778 Transcript splice_acceptor_variant - - - - - - rs231243 19:36243813 A 55957 NM_019104.2 Transcript splice_acceptor_variant - - - - - - rs231243 19:36243813 A ENSESTG00000011477 ENSESTT00000028793 Transcript upstream_gene_variant - - - - - - DISTANCE=4660 rs231243 19:36243813 A ENSESTG00000011061 ENSESTT00000027756 Transcript splice_acceptor_variant - - - - - - rs807492 19:36284832 T ENSESTG00000011433 ENSESTT00000028693 Transcript intron_variant - - - - - - rs807492 19:36284832 T ENSESTG00000011433 ENSESTT00000028691 Transcript intron_variant - - - - - - rs807492 19:36284832 T ENSESTG00000011433 ENSESTT00000028688 Transcript intron_variant - - - - - - rs807493 19:36284946 T ENSESTG00000011433 ENSESTT00000028693 Transcript intron_variant - - - - - - rs807493 19:36284946 T ENSESTG00000011433 ENSESTT00000028691 Transcript intron_variant - - - - - - rs807493 19:36284946 T ENSESTG00000011433 ENSESTT00000028688 Transcript intron_variant - - - - - - rs2619201 19:36286884 T 58510 NM_021232.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4008 rs2619201 19:36286884 T ENSESTG00000011433 ENSESTT00000028693 Transcript intron_variant - - - - - - rs2619201 19:36286884 T ENSESTG00000011433 ENSESTT00000028691 Transcript intron_variant - - - - - - rs2619201 19:36286884 T ENSESTG00000011421 ENSESTT00000028657 Transcript downstream_gene_variant - - - - - - DISTANCE=4008 rs2619201 19:36286884 T ENSESTG00000011433 ENSESTT00000028688 Transcript intron_variant - - - - - - rs2619201 19:36286884 T ENSESTG00000011421 ENSESTT00000028671 Transcript downstream_gene_variant - - - - - - DISTANCE=4008 rs2619201 19:36286884 T ENSESTG00000011421 ENSESTT00000028668 Transcript downstream_gene_variant - - - - - - DISTANCE=4008 rs2619201 19:36286884 T CCDS12478.1 CCDS12478.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4056 rs2619201 19:36286884 T ENSESTG00000011138 ENSESTT00000027947 Transcript upstream_gene_variant - - - - - - DISTANCE=4006 rs2520313 19:36287678 A 58510 NM_021232.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3214 rs2520313 19:36287678 A ENSESTG00000011433 ENSESTT00000028693 Transcript intron_variant - - - - - - rs2520313 19:36287678 A ENSESTG00000011433 ENSESTT00000028691 Transcript intron_variant - - - - - - rs2520313 19:36287678 A ENSESTG00000011421 ENSESTT00000028657 Transcript downstream_gene_variant - - - - - - DISTANCE=3214 rs2520313 19:36287678 A ENSESTG00000011433 ENSESTT00000028688 Transcript intron_variant - - - - - - rs2520313 19:36287678 A ENSESTG00000011421 ENSESTT00000028671 Transcript downstream_gene_variant - - - - - - DISTANCE=3214 rs2520313 19:36287678 A ENSESTG00000011421 ENSESTT00000028668 Transcript downstream_gene_variant - - - - - - DISTANCE=3214 rs2520313 19:36287678 A CCDS12478.1 CCDS12478.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3262 rs2520313 19:36287678 A ENSESTG00000011138 ENSESTT00000027947 Transcript upstream_gene_variant - - - - - - DISTANCE=3212 rs436842 19:36334594 A CCDS32996.1 CCDS32996.1 Transcript intron_variant - - - - - - rs436842 19:36334594 A ENSESTG00000011400 ENSESTT00000028630 Transcript downstream_gene_variant - - - - - - DISTANCE=226 rs436842 19:36334594 A ENSESTG00000011400 ENSESTT00000028622 Transcript downstream_gene_variant - - - - - - DISTANCE=694 rs436842 19:36334594 A ENSESTG00000011406 ENSESTT00000028636 Transcript upstream_gene_variant - - - - - - DISTANCE=176 rs436842 19:36334594 A 4868 NM_004646.3 Transcript intron_variant - - - - - - rs382789 19:36355595 G 333 NM_005166.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3806 rs382789 19:36355595 G 84063 NM_199180.2 Transcript missense_variant 1983 1771 591 K/E Aaa/Gaa - PolyPhen=benign;SIFT=tolerated rs382789 19:36355595 G ENSESTG00000011337 ENSESTT00000028469 Transcript intron_variant - - - - - - rs382789 19:36355595 G CCDS32997.1 CCDS32997.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3944 rs382789 19:36355595 G ENSESTG00000011190 ENSESTT00000028125 Transcript upstream_gene_variant - - - - - - DISTANCE=3206 rs382789 19:36355595 G ENSESTG00000011190 ENSESTT00000028124 Transcript upstream_gene_variant - - - - - - DISTANCE=3206 rs382789 19:36355595 G CCDS12479.1 CCDS12479.1 Transcript missense_variant 1771 1771 591 K/E Aaa/Gaa - PolyPhen=benign;SIFT=tolerated rs382789 19:36355595 G 84063 NM_032123.5 Transcript missense_variant 1983 1771 591 K/E Aaa/Gaa - PolyPhen=benign;SIFT=tolerated rs382789 19:36355595 G ENSESTG00000011151 ENSESTT00000028006 Transcript missense_variant 296 202 68 K/E Aaa/Gaa - rs382789 19:36355595 G CCDS12480.1 CCDS12480.1 Transcript missense_variant 1621 1621 541 K/E Aaa/Gaa - PolyPhen=benign;SIFT=tolerated rs382789 19:36355595 G ENSESTG00000011190 ENSESTT00000028122 Transcript upstream_gene_variant - - - - - - DISTANCE=3206 rs382789 19:36355595 G ENSESTG00000011151 ENSESTT00000028002 Transcript missense_variant 497 304 102 K/E Aaa/Gaa - rs382789 19:36355595 G ENSESTG00000011190 ENSESTT00000028126 Transcript upstream_gene_variant - - - - - - DISTANCE=3206 rs382789 19:36355595 G ENSESTG00000011190 ENSESTT00000028141 Transcript upstream_gene_variant - - - - - - DISTANCE=3831 rs382789 19:36355595 G ENSESTG00000011151 ENSESTT00000027987 Transcript downstream_gene_variant - - - - - - DISTANCE=3101 rs382789 19:36355595 G 84063 NM_199179.2 Transcript missense_variant 1833 1621 541 K/E Aaa/Gaa - PolyPhen=benign;SIFT=tolerated rs382789 19:36355595 G CCDS12481.1 CCDS12481.1 Transcript missense_variant 1771 1771 591 K/E Aaa/Gaa - PolyPhen=benign;SIFT=tolerated rs382789 19:36355595 G 333 NM_001024807.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3806 rs8104979 19:36382754 G CCDS42552.1 CCDS42552.1 Transcript intron_variant - - - - - - rs8104979 19:36382754 G 84807 NM_139239.1 Transcript intron_variant - - - - - - rs8104979 19:36382754 G ENSESTG00000011299 ENSESTT00000028406 Transcript intron_variant - - - - - - rs8104979 19:36382754 G ENSESTG00000011299 ENSESTT00000028399 Transcript downstream_gene_variant - - - - - - DISTANCE=3982 rs8104979 19:36382754 G ENSESTG00000011299 ENSESTT00000028396 Transcript intron_variant - - - - - - rs8104979 19:36382754 G ENSESTG00000011299 ENSESTT00000028367 Transcript downstream_gene_variant - - - - - - DISTANCE=4398 rs12980027 19:36382876 C CCDS42552.1 CCDS42552.1 Transcript intron_variant - - - - - - rs12980027 19:36382876 C 84807 NM_139239.1 Transcript intron_variant - - - - - - rs12980027 19:36382876 C ENSESTG00000011299 ENSESTT00000028406 Transcript intron_variant - - - - - - rs12980027 19:36382876 C ENSESTG00000011299 ENSESTT00000028399 Transcript downstream_gene_variant - - - - - - DISTANCE=3860 rs12980027 19:36382876 C ENSESTG00000011299 ENSESTT00000028396 Transcript intron_variant - - - - - - rs12980027 19:36382876 C ENSESTG00000011299 ENSESTT00000028367 Transcript downstream_gene_variant - - - - - - DISTANCE=4276 rs34671697 19:36420324 A - - - intergenic_variant - - - - - - rs4805148 19:36432569 C ENSESTG00000011255 ENSESTT00000028204 Transcript downstream_gene_variant - - - - - - DISTANCE=4641 rs4805148 19:36432569 C ENSESTG00000011262 ENSESTT00000028222 Transcript intron_variant - - - - - - rs4805148 19:36432569 C 79414 NM_024509.1 Transcript intron_variant - - - - - - rs4805148 19:36432569 C ENSESTG00000011255 ENSESTT00000028197 Transcript downstream_gene_variant - - - - - - DISTANCE=4875 rs4805148 19:36432569 C ENSESTG00000011258 ENSESTT00000028209 Transcript downstream_gene_variant - - - - - - DISTANCE=1793 rs4805148 19:36432569 C CCDS12483.1 CCDS12483.1 Transcript intron_variant - - - - - - rs4805148 19:36432569 C ENSESTG00000011255 ENSESTT00000028201 Transcript downstream_gene_variant - - - - - - DISTANCE=4553 rs4805148 19:36432569 C ENSESTG00000011268 ENSESTT00000028236 Transcript intron_variant - - - - - - rs7246689 19:36441775 C ENSESTG00000011267 ENSESTT00000028228 Transcript intron_variant - - - - - - rs3942203 19:36444719 C ENSESTG00000011267 ENSESTT00000028228 Transcript intron_variant - - - - - - rs1997538 19:36447309 C ENSESTG00000011267 ENSESTT00000028228 Transcript intron_variant - - - - - - rs6510514 19:36462289 C - - - intergenic_variant - - - - - - rs1269206 19:36489963 C - ENSR00000044132 RegulatoryFeature regulatory_region_variant - - - - - - rs1269206 19:36489963 C CCDS42553.1 CCDS42553.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4276 rs1269206 19:36489963 C CCDS32999.1 CCDS32999.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3439 rs1269206 19:36489963 C 163183 NM_001039876.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4039 rs1269206 19:36489963 C 644096 NM_001042631.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2743 rs3108557 19:37175623 G ENSESTG00000003779 ENSESTT00000009523 Transcript upstream_gene_variant - - - - - - DISTANCE=2956 rs3108557 19:37175623 G ENSESTG00000003779 ENSESTT00000009507 Transcript upstream_gene_variant - - - - - - DISTANCE=2838 rs3108557 19:37175623 G 163081 NM_152603.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4679 rs3108557 19:37175623 G ENSESTG00000003779 ENSESTT00000009515 Transcript upstream_gene_variant - - - - - - DISTANCE=2838 rs3108557 19:37175623 G ENSESTG00000003779 ENSESTT00000009522 Transcript upstream_gene_variant - - - - - - DISTANCE=2927 rs3108557 19:37175623 G ENSESTG00000003779 ENSESTT00000009511 Transcript upstream_gene_variant - - - - - - DISTANCE=2838 rs3108557 19:37175623 G ENSESTG00000003779 ENSESTT00000009521 Transcript upstream_gene_variant - - - - - - DISTANCE=2907 rs3108557 19:37175623 G ENSESTG00000003779 ENSESTT00000009518 Transcript upstream_gene_variant - - - - - - DISTANCE=2891 rs548232 19:37359903 T ENSESTG00000003818 ENSESTT00000009608 Transcript intron_variant - - - - - - rs548232 19:37359903 T ENSESTG00000003818 ENSESTT00000009620 Transcript intron_variant - - - - - - rs548232 19:37359903 T ENSESTG00000003818 ENSESTT00000009629 Transcript intron_variant - - - - - - rs548232 19:37359903 T 25850 NM_001242476.1 Transcript intron_variant - - - - - - rs548232 19:37359903 T 25850 NM_001242475.1 Transcript intron_variant - - - - - - rs548232 19:37359903 T 25850 NM_001242472.1 Transcript intron_variant - - - - - - rs548232 19:37359903 T 25850 NM_001242474.1 Transcript intron_variant - - - - - - rs548232 19:37359903 T ENSESTG00000003818 ENSESTT00000009627 Transcript intron_variant - - - - - - rs548232 19:37359903 T 25850 NR_038362.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs548232 19:37359903 T ENSESTG00000003818 ENSESTT00000009613 Transcript intron_variant - - - - - - rs548232 19:37359903 T ENSESTG00000003818 ENSESTT00000009623 Transcript intron_variant - - - - - - rs548232 19:37359903 T 25850 NM_003419.4 Transcript intron_variant - - - - - - rs506758 19:37404856 G 374900 NM_001204837.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2375 rs506758 19:37404856 G 374900 NM_001204836.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2375 rs506758 19:37404856 G 374900 NM_001204838.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2375 rs506758 19:37404856 G ENSESTG00000003834 ENSESTT00000009686 Transcript upstream_gene_variant - - - - - - DISTANCE=2410 rs506758 19:37404856 G 374899 NM_001037232.3 Transcript intron_variant - - - - - - rs506758 19:37404856 G 374900 NM_001204839.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2375 rs506758 19:37404856 G 374900 NM_198539.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2375 rs506758 19:37404856 G ENSESTG00000003856 ENSESTT00000009711 Transcript intron_variant - - - - - - rs506758 19:37404856 G CCDS42557.1 CCDS42557.1 Transcript intron_variant - - - - - - rs506758 19:37404856 G ENSESTG00000003834 ENSESTT00000009680 Transcript upstream_gene_variant - - - - - - DISTANCE=2410 rs506758 19:37404856 G ENSESTG00000003834 ENSESTT00000009665 Transcript upstream_gene_variant - - - - - - DISTANCE=2378 rs506758 19:37404856 G 374899 NM_001171979.1 Transcript intron_variant - - - - - - rs506758 19:37404856 G ENSESTG00000003834 ENSESTT00000009673 Transcript upstream_gene_variant - - - - - - DISTANCE=2397 rs506758 19:37404856 G 374900 NM_001204835.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2375 rs320883 19:37739498 A ENSESTG00000011051 ENSESTT00000027717 Transcript downstream_gene_variant - - - - - - DISTANCE=4524 rs320883 19:37739498 A CCDS12501.1 CCDS12501.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4932 rs320883 19:37739498 A ENSESTG00000011051 ENSESTT00000027715 Transcript downstream_gene_variant - - - - - - DISTANCE=4524 rs320883 19:37739498 A 163087 NM_152604.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4924 rs320883 19:37739498 A ENSESTG00000011064 ENSESTT00000027742 Transcript upstream_gene_variant - - - - - - DISTANCE=3330 rs320883 19:37739498 A ENSESTG00000011051 ENSESTT00000027721 Transcript downstream_gene_variant - - - - - - DISTANCE=4524 rs320883 19:37739498 A ENSESTG00000011051 ENSESTT00000027711 Transcript downstream_gene_variant - - - - - - DISTANCE=4524 rs320883 19:37739498 A ENSESTG00000011064 ENSESTT00000027737 Transcript upstream_gene_variant - - - - - - DISTANCE=3316 rs657614 19:37844932 G 284459 NM_181786.2 Transcript intron_variant - - - - - - rs657614 19:37844932 G ENSESTG00000011079 ENSESTT00000027825 Transcript intron_variant - - - - - - rs657614 19:37844932 G ENSESTG00000011079 ENSESTT00000027818 Transcript intron_variant - - - - - - rs657614 19:37844932 G ENSESTG00000011079 ENSESTT00000027827 Transcript intron_variant - - - - - - rs657614 19:37844932 G ENSESTG00000011079 ENSESTT00000027844 Transcript intron_variant - - - - - - rs657614 19:37844932 G ENSESTG00000011079 ENSESTT00000027836 Transcript intron_variant - - - - - - rs657614 19:37844932 G CCDS12502.1 CCDS12502.1 Transcript intron_variant - - - - - - rs657614 19:37844932 G ENSESTG00000011079 ENSESTT00000027806 Transcript intron_variant - - - - - - rs7252765 19:38377409 T CCDS46063.1 CCDS46063.1 Transcript missense_variant 6785 6785 2262 V/E gTa/gAa - PolyPhen=unknown rs7252765 19:38377409 T 83889 NM_031951.3 Transcript missense_variant 7010 6785 2262 V/E gTa/gAa - PolyPhen=unknown rs535703 19:39653237 C 10298 NM_001014831.2 Transcript intron_variant - - - - - - rs535703 19:39653237 C 10298 NM_001014834.2 Transcript intron_variant - - - - - - rs535703 19:39653237 C ENSESTG00000032259 ENSESTT00000081530 Transcript intron_variant - - - - - - rs535703 19:39653237 C 10298 NM_005884.3 Transcript intron_variant - - - - - - rs535703 19:39653237 C 10298 NM_001014832.1 Transcript intron_variant - - - - - - rs535703 19:39653237 C 10298 NM_001014835.1 Transcript intron_variant - - - - - - rs535703 19:39653237 C ENSESTG00000032259 ENSESTT00000081502 Transcript intron_variant - - - - - - rs535703 19:39653237 C ENSESTG00000032259 ENSESTT00000081512 Transcript intron_variant - - - - - - rs535703 19:39653237 C ENSESTG00000032259 ENSESTT00000081538 Transcript intron_variant - - - - - - rs10775535 19:39745181 T - ENSR00000216518 RegulatoryFeature regulatory_region_variant - - - - - - rs10775535 19:39745181 T - - - intergenic_variant - - - - - - rs251908 19:39764449 G 282616 NM_172138.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3717 rs251908 19:39764449 G CCDS42567.1 CCDS42567.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3796 rs1860134 19:40149297 A 148003 NM_001190441.1 Transcript missense_variant 334 290 97 L/H cTc/cAc - PolyPhen=benign;SIFT=tolerated rs1860134 19:40149297 A CCDS54267.1 CCDS54267.1 Transcript missense_variant 290 290 97 L/H cTc/cAc - PolyPhen=benign;SIFT=tolerated rs1860134 19:40149297 A ENSESTG00000033286 ENSESTT00000084065 Transcript downstream_gene_variant - - - - - - DISTANCE=2782 rs1860134 19:40149297 A ENSESTG00000033291 ENSESTT00000084089 Transcript missense_variant 335 290 97 L/H cTc/cAc - PolyPhen=benign;SIFT=tolerated rs10404227 19:40239947 C - - - intergenic_variant - - - - - - rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000074913 Transcript downstream_gene_variant - - - - - - DISTANCE=2477 rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000074977 Transcript downstream_gene_variant - - - - - - DISTANCE=2477 rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000074915 Transcript downstream_gene_variant - - - - - - DISTANCE=4689 rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000074799 Transcript downstream_gene_variant - - - - - - DISTANCE=4689 rs4574034 19:40737242 C 208 NM_001626.4 Transcript 3_prime_UTR_variant 4282 - - - - - rs4574034 19:40737242 C CCDS12551.2 CCDS12551.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4694 rs4574034 19:40737242 C CCDS12552.1 CCDS12552.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2537 rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000074842 Transcript downstream_gene_variant - - - - - - DISTANCE=1820 rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000075007 Transcript downstream_gene_variant - - - - - - DISTANCE=2477 rs4574034 19:40737242 C 208 NM_001243028.1 Transcript 3_prime_UTR_variant 4152 - - - - - rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000074773 Transcript downstream_gene_variant - - - - - - DISTANCE=2477 rs4574034 19:40737242 C 208 NM_001243027.1 Transcript 3_prime_UTR_variant 4245 - - - - - rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000074780 Transcript downstream_gene_variant - - - - - - DISTANCE=2477 rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000074991 Transcript downstream_gene_variant - - - - - - DISTANCE=4689 rs4574034 19:40737242 C ENSESTG00000029650 ENSESTT00000074798 Transcript downstream_gene_variant - - - - - - DISTANCE=4689 rs4574034 19:40737242 C 79935 NM_024877.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4645 rs268683 19:40931865 C - ENSR00000641645 RegulatoryFeature regulatory_region_variant - - - - - - rs268683 19:40931865 C 29950 NM_013376.3 Transcript 5_prime_UTR_variant 68 - - - - - rs268683 19:40931865 C CCDS12557.1 CCDS12557.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2412 rs338592 19:41704832 G CCDS12573.1 CCDS12573.1 Transcript intron_variant - - - - - - rs338592 19:41704832 G ENSESTG00000021085 ENSESTT00000052933 Transcript intron_variant - - - - - - rs338592 19:41704832 G 29785 NM_030622.6 Transcript intron_variant - - - - - - rs338592 19:41704832 G ENSESTG00000021085 ENSESTT00000052942 Transcript upstream_gene_variant - - - - - - DISTANCE=2366 rs7249222 19:41743861 G ENSESTG00000021108 ENSESTT00000053272 Transcript 5_prime_UTR_variant 785 - - - - - rs7249222 19:41743861 G ENSESTG00000021108 ENSESTT00000053281 Transcript 5_prime_UTR_variant 785 - - - - - rs7249222 19:41743861 G 558 NM_021913.3 Transcript missense_variant 986 796 266 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs7249222 19:41743861 G ENSESTG00000021108 ENSESTT00000053286 Transcript 5_prime_UTR_variant 785 - - - - - rs7249222 19:41743861 G CCDS12574.1 CCDS12574.1 Transcript missense_variant 796 796 266 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs7249222 19:41743861 G CCDS12575.1 CCDS12575.1 Transcript missense_variant 796 796 266 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs7249222 19:41743861 G 558 NM_001699.4 Transcript missense_variant 986 796 266 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs4803450 19:41746748 C ENSESTG00000021108 ENSESTT00000053272 Transcript intron_variant - - - - - - rs4803450 19:41746748 C ENSESTG00000021108 ENSESTT00000053281 Transcript intron_variant - - - - - - rs4803450 19:41746748 C 558 NM_021913.3 Transcript intron_variant - - - - - - rs4803450 19:41746748 C ENSESTG00000021108 ENSESTT00000053286 Transcript intron_variant - - - - - - rs4803450 19:41746748 C CCDS12574.1 CCDS12574.1 Transcript intron_variant - - - - - - rs4803450 19:41746748 C CCDS12575.1 CCDS12575.1 Transcript intron_variant - - - - - - rs4803450 19:41746748 C 558 NM_001699.4 Transcript intron_variant - - - - - - rs2317470 19:42223451 C ENSESTG00000022049 ENSESTT00000055645 Transcript intron_variant - - - - - - rs2317470 19:42223451 C ENSESTG00000022049 ENSESTT00000055731 Transcript downstream_gene_variant - - - - - - DISTANCE=2037 rs2317470 19:42223451 C ENSESTG00000022049 ENSESTT00000055771 Transcript intron_variant - - - - - - rs2317470 19:42223451 C ENSESTG00000022049 ENSESTT00000055691 Transcript downstream_gene_variant - - - - - - DISTANCE=1902 rs2317470 19:42223451 C 1048 NM_004363.2 Transcript intron_variant - - - - - - rs2317470 19:42223451 C CCDS12584.1 CCDS12584.1 Transcript intron_variant - - - - - - rs2317470 19:42223451 C ENSESTG00000022049 ENSESTT00000055750 Transcript downstream_gene_variant - - - - - - DISTANCE=1236 rs10415627 19:42382729 G 9138 NM_198977.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4538 rs10415627 19:42382729 G ENSESTG00000020889 ENSESTT00000053017 Transcript upstream_gene_variant - - - - - - DISTANCE=4550 rs10415627 19:42382729 G ENSESTG00000020889 ENSESTT00000053040 Transcript upstream_gene_variant - - - - - - DISTANCE=4550 rs10415627 19:42382729 G ENSESTG00000020821 ENSESTT00000052325 Transcript intron_variant - - - - - - rs10415627 19:42382729 G 9138 NM_004706.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4538 rs10415627 19:42382729 G 973 NM_021601.3 Transcript intron_variant - - - - - - rs10415627 19:42382729 G CCDS46088.1 CCDS46088.1 Transcript intron_variant - - - - - - rs10415627 19:42382729 G ENSESTG00000020889 ENSESTT00000053072 Transcript upstream_gene_variant - - - - - - DISTANCE=4561 rs10415627 19:42382729 G CCDS12589.1 CCDS12589.1 Transcript intron_variant - - - - - - rs10415627 19:42382729 G ENSESTG00000020889 ENSESTT00000053091 Transcript upstream_gene_variant - - - - - - DISTANCE=4561 rs10415627 19:42382729 G ENSESTG00000020889 ENSESTT00000053077 Transcript upstream_gene_variant - - - - - - DISTANCE=4561 rs10415627 19:42382729 G 973 NM_001783.3 Transcript intron_variant - - - - - - rs10415627 19:42382729 G ENSESTG00000020889 ENSESTT00000052407 Transcript upstream_gene_variant - - - - - - DISTANCE=4538 rs10415627 19:42382729 G ENSESTG00000020889 ENSESTT00000052492 Transcript upstream_gene_variant - - - - - - DISTANCE=4550 rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000053017 Transcript intron_variant - - - - - - rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000053040 Transcript intron_variant - - - - - - rs891168 19:42389249 A ENSESTG00000020821 ENSESTT00000052325 Transcript downstream_gene_variant - - - - - - DISTANCE=3811 rs891168 19:42389249 A 9138 NM_004706.3 Transcript intron_variant - - - - - - rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000053072 Transcript intron_variant - - - - - - rs891168 19:42389249 A CCDS12591.1 CCDS12591.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2905 rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000053091 Transcript intron_variant - - - - - - rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000053077 Transcript intron_variant - - - - - - rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000053186 Transcript intron_variant - - - - - - rs891168 19:42389249 A CCDS12592.1 CCDS12592.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2905 rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000053170 Transcript intron_variant - - - - - - rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000052492 Transcript intron_variant - - - - - - rs891168 19:42389249 A 9138 NM_198977.1 Transcript intron_variant - - - - - - rs891168 19:42389249 A 9138 NM_199002.1 Transcript intron_variant - - - - - - rs891168 19:42389249 A CCDS12590.1 CCDS12590.1 Transcript intron_variant - - - - - - rs891168 19:42389249 A 973 NM_021601.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3810 rs891168 19:42389249 A CCDS46088.1 CCDS46088.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4202 rs891168 19:42389249 A CCDS12589.1 CCDS12589.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4202 rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000053206 Transcript intron_variant - - - - - - rs891168 19:42389249 A 973 NM_001783.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3810 rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000053181 Transcript intron_variant - - - - - - rs891168 19:42389249 A ENSESTG00000020889 ENSESTT00000052407 Transcript intron_variant - - - - - - rs4255880 19:42545988 G CCDS12595.1 CCDS12595.1 Transcript intron_variant - - - - - - rs4255880 19:42545988 G 2901 NM_002088.4 Transcript intron_variant - - - - - - rs851609 19:42736267 G 116115 NM_133444.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3914 rs851609 19:42736267 G CCDS12599.1 CCDS12599.1 Transcript synonymous_variant 1320 1320 440 L ctT/ctC - rs851609 19:42736267 G 2931 NM_019884.2 Transcript synonymous_variant 1439 1320 440 L ctT/ctC - rs851610 19:42739683 T CCDS12599.1 CCDS12599.1 Transcript intron_variant - - - - - - rs851610 19:42739683 T 2931 NM_019884.2 Transcript intron_variant - - - - - - rs10422654 19:42971059 C ENSESTG00000021623 ENSESTT00000054344 Transcript intron_variant - - - - - - rs10422654 19:42971059 C ENSESTG00000021623 ENSESTT00000054314 Transcript intron_variant - - - - - - rs10422654 19:42971059 C ENSESTG00000021623 ENSESTT00000054330 Transcript intron_variant - - - - - - rs10422654 19:42971059 C ENSESTG00000021623 ENSESTT00000054285 Transcript intron_variant - - - - - - rs10422654 19:42971059 C 100996307 XM_003846290.1 Transcript intron_variant - - - - - - rs10412791 19:42991260 T ENSESTG00000021623 ENSESTT00000054344 Transcript downstream_gene_variant - - - - - - DISTANCE=1635 rs10412791 19:42991260 T ENSESTG00000021623 ENSESTT00000054314 Transcript intron_variant - - - - - - rs10412791 19:42991260 T ENSESTG00000021623 ENSESTT00000054330 Transcript downstream_gene_variant - - - - - - DISTANCE=1882 rs10412791 19:42991260 T ENSESTG00000021623 ENSESTT00000054285 Transcript downstream_gene_variant - - - - - - DISTANCE=1514 rs10412791 19:42991260 T 100996307 XM_003846290.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G CCDS54272.1 CCDS54272.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G CCDS12609.1 CCDS12609.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G 634 NM_001184813.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G CCDS54274.1 CCDS54274.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G 634 NM_001024912.2 Transcript intron_variant - - - - - - rs7245968 19:43024906 G 100996307 XM_003846290.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G CCDS46089.1 CCDS46089.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G CCDS54273.1 CCDS54273.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G ENSESTG00000021623 ENSESTT00000054314 Transcript intron_variant - - - - - - rs7245968 19:43024906 G 634 NM_001184816.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G 634 NM_001712.4 Transcript intron_variant - - - - - - rs7245968 19:43024906 G 634 NM_001205344.1 Transcript intron_variant - - - - - - rs7245968 19:43024906 G 634 NM_001184815.1 Transcript intron_variant - - - - - - rs1210050 19:43559829 C ENSESTG00000020314 ENSESTT00000050920 Transcript intron_variant - - - - - - rs1210050 19:43559829 C ENSESTG00000020227 ENSESTT00000050894 Transcript intron_variant - - - - - - rs1210050 19:43559829 C ENSESTG00000020323 ENSESTT00000050941 Transcript intron_variant - - - - - - rs1210050 19:43559829 C ENSESTG00000020227 ENSESTT00000050762 Transcript intron_variant - - - - - - rs2682546 19:44000810 A CCDS12621.2 CCDS12621.2 Transcript intron_variant - - - - - - rs2682546 19:44000810 A 653583 NM_198850.3 Transcript intron_variant - - - - - - rs2682557 19:44047826 A ENSESTG00000020091 ENSESTT00000050495 Transcript downstream_gene_variant - - - - - - DISTANCE=3277 rs2682557 19:44047826 A CCDS12624.1 CCDS12624.1 Transcript missense_variant 1726 1726 576 N/Y Aat/Tat - PolyPhen=benign;SIFT=tolerated rs2682557 19:44047826 A 7515 NM_006297.2 Transcript missense_variant 1846 1726 576 N/Y Aat/Tat - PolyPhen=benign;SIFT=tolerated rs449664 19:44504804 G 7711 NM_001260486.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2327 rs449664 19:44504804 G ENSESTG00000022035 ENSESTT00000055616 Transcript downstream_gene_variant - - - - - - DISTANCE=4276 rs449664 19:44504804 G ENSESTG00000022088 ENSESTT00000055743 Transcript upstream_gene_variant - - - - - - DISTANCE=2326 rs449664 19:44504804 G 7711 NM_001260488.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2327 rs449664 19:44504804 G ENSESTG00000022035 ENSESTT00000055556 Transcript downstream_gene_variant - - - - - - DISTANCE=4401 rs449664 19:44504804 G 7711 NM_198089.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2327 rs449664 19:44504804 G ENSESTG00000022035 ENSESTT00000055596 Transcript downstream_gene_variant - - - - - - DISTANCE=4276 rs449664 19:44504804 G ENSESTG00000022088 ENSESTT00000055722 Transcript upstream_gene_variant - - - - - - DISTANCE=2293 rs449664 19:44504804 G ENSESTG00000022035 ENSESTT00000055515 Transcript downstream_gene_variant - - - - - - DISTANCE=4276 rs449664 19:44504804 G 7773 NM_006300.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2273 rs449664 19:44504804 G CCDS12634.1 CCDS12634.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3178 rs449664 19:44504804 G 7711 NM_003445.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2327 rs449664 19:44504804 G CCDS58668.1 CCDS58668.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3178 rs449664 19:44504804 G 7711 NM_001260487.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2327 rs203712 19:45168400 A ENSESTG00000022520 ENSESTT00000056985 Transcript downstream_gene_variant - - - - - - DISTANCE=3183 rs203712 19:45168400 A CCDS12640.1 CCDS12640.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3322 rs203712 19:45168400 A ENSESTG00000022520 ENSESTT00000057003 Transcript downstream_gene_variant - - - - - - DISTANCE=3277 rs203712 19:45168400 A ENSESTG00000022520 ENSESTT00000057030 Transcript downstream_gene_variant - - - - - - DISTANCE=2944 rs203712 19:45168400 A 5817 NM_001135768.1 Transcript 3_prime_UTR_variant 4740 - - - - - rs203712 19:45168400 A 5817 NM_001135769.1 Transcript 3_prime_UTR_variant 4716 - - - - - rs203712 19:45168400 A 5817 NM_006505.3 Transcript 3_prime_UTR_variant 4875 - - - - - rs203712 19:45168400 A CCDS46105.1 CCDS46105.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3322 rs203712 19:45168400 A ENSESTG00000022520 ENSESTT00000057014 Transcript downstream_gene_variant - - - - - - DISTANCE=2947 rs203712 19:45168400 A CCDS46106.1 CCDS46106.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3322 rs4803794 19:45561063 G ENSESTG00000021491 ENSESTT00000053935 Transcript downstream_gene_variant - - - - - - DISTANCE=4736 rs4803794 19:45561063 G CCDS12652.2 CCDS12652.2 Transcript missense_variant 520 520 174 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs4803794 19:45561063 G ENSESTG00000021491 ENSESTT00000054053 Transcript downstream_gene_variant - - - - - - DISTANCE=20 rs4803794 19:45561063 G ENSESTG00000021558 ENSESTT00000054311 Transcript upstream_gene_variant - - - - - - DISTANCE=1493 rs4803794 19:45561063 G ENSESTG00000021491 ENSESTT00000054032 Transcript downstream_gene_variant - - - - - - DISTANCE=20 rs4803794 19:45561063 G 11129 NM_007056.2 Transcript missense_variant 618 520 174 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs4803794 19:45561063 G ENSESTG00000021558 ENSESTT00000054329 Transcript upstream_gene_variant - - - - - - DISTANCE=2586 rs4803794 19:45561063 G ENSESTG00000021558 ENSESTT00000054351 Transcript upstream_gene_variant - - - - - - DISTANCE=2803 rs4803794 19:45561063 G ENSESTG00000021558 ENSESTT00000054273 Transcript upstream_gene_variant - - - - - - DISTANCE=16 rs674361 19:46936399 G - - - intergenic_variant - - - - - - rs7245589 19:46994769 C 100506012 NM_001205281.1 Transcript intron_variant - - - - - - rs7245589 19:46994769 C 57469 NM_020709.1 Transcript 3_prime_UTR_variant 4401 - - - - - rs7245589 19:46994769 C ENSESTG00000018944 ENSESTT00000047684 Transcript upstream_gene_variant - - - - - - DISTANCE=1392 rs7245589 19:46994769 C ENSESTG00000018944 ENSESTT00000047678 Transcript intron_variant - - - - - - rs7245589 19:46994769 C ENSESTG00000018417 ENSESTT00000046340 Transcript upstream_gene_variant - - - - - - DISTANCE=338 rs314665 19:47177913 G ENSESTG00000018750 ENSESTT00000047560 Transcript missense_variant 2519 2033 678 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs314665 19:47177913 G ENSESTG00000018750 ENSESTT00000047505 Transcript missense_variant 2634 2504 835 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs314665 19:47177913 G 100506068 NR_040041.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3315 rs314665 19:47177913 G 25865 NM_001079882.1 Transcript missense_variant 2583 2033 678 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs314665 19:47177913 G ENSESTG00000018750 ENSESTT00000047483 Transcript missense_variant 2516 2033 678 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs314665 19:47177913 G ENSESTG00000018750 ENSESTT00000047548 Transcript missense_variant 1556 1064 355 V/A gTg/gCg - rs314665 19:47177913 G ENSESTG00000018521 ENSESTT00000046617 Transcript intron_variant - - - - - - rs314665 19:47177913 G ENSESTG00000018521 ENSESTT00000046625 Transcript intron_variant - - - - - - rs314665 19:47177913 G 25865 NM_001079880.1 Transcript missense_variant 2982 2504 835 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs314665 19:47177913 G ENSESTG00000018750 ENSESTT00000047583 Transcript missense_variant 1369 1064 355 V/A gTg/gCg - rs314665 19:47177913 G 25865 NM_016457.4 Transcript missense_variant 3261 2504 835 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs314665 19:47177913 G CCDS12689.1 CCDS12689.1 Transcript missense_variant 2504 2504 835 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs314665 19:47177913 G 25865 NM_001079881.1 Transcript missense_variant 2846 2504 835 V/A gTg/gCg - PolyPhen=benign;SIFT=tolerated rs314665 19:47177913 G 100506068 NR_040042.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs314665 19:47177913 G ENSESTG00000018750 ENSESTT00000047607 Transcript downstream_gene_variant - - - - - - DISTANCE=374 rs12611413 19:47525931 G ENSESTG00000020837 ENSESTT00000052304 Transcript intron_variant - - - - - - rs12611413 19:47525931 G 4861 NM_002517.2 Transcript intron_variant - - - - - - rs12611413 19:47525931 G CCDS12694.1 CCDS12694.1 Transcript intron_variant - - - - - - rs6509326 19:47843309 T 27202 NM_018485.1 Transcript intron_variant - - - - - - rs6509326 19:47843309 T ENSESTG00000021183 ENSESTT00000053253 Transcript intron_variant - - - - - - rs6509326 19:47843309 T CCDS12699.1 CCDS12699.1 Transcript upstream_gene_variant - - - - - - DISTANCE=748 rs6509326 19:47843309 T ENSESTG00000021183 ENSESTT00000053200 Transcript intron_variant - - - - - - rs2914012 19:48068047 C - - - intergenic_variant - - - - - - rs12976132 19:48075678 G - - - intergenic_variant - - - - - - rs2914019 19:48128923 G ENSESTG00000021635 ENSESTT00000054296 Transcript intron_variant - - - - - - rs2914019 19:48128923 G 29998 NM_015711.3 Transcript intron_variant - - - - - - rs2914019 19:48128923 G ENSESTG00000021359 ENSESTT00000053625 Transcript intron_variant - - - - - - rs2914019 19:48128923 G ENSESTG00000021359 ENSESTT00000053634 Transcript intron_variant - - - - - - rs296394 19:48366083 T - - - intergenic_variant - - - - - - rs6509347 19:48393990 G CCDS12707.1 CCDS12707.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4476 rs6509347 19:48393990 G ENSESTG00000021478 ENSESTT00000053905 Transcript upstream_gene_variant - - - - - - DISTANCE=4462 rs6509347 19:48393990 G 6822 NM_003167.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4336 rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052943 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052819 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052767 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052856 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000018755 ENSESTT00000047253 Transcript upstream_gene_variant - - - - - - DISTANCE=2207 rs415465 19:48646993 T 3978 NM_000234.1 Transcript intron_variant - - - - - - rs415465 19:48646993 T CCDS12711.1 CCDS12711.1 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052950 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052866 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052824 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052782 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052804 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052850 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052938 Transcript intron_variant - - - - - - rs415465 19:48646993 T ENSESTG00000020846 ENSESTT00000052831 Transcript intron_variant - - - - - - rs838132 19:49259979 G 26291 NM_019113.2 Transcript intron_variant - - - - - - rs838132 19:49259979 G 2523 NM_000148.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1332 rs838132 19:49259979 G CCDS12734.1 CCDS12734.1 Transcript intron_variant - - - - - - rs838132 19:49259979 G ENSESTG00000019405 ENSESTT00000048736 Transcript intron_variant - - - - - - rs11083954 19:49441366 T CCDS12741.1 CCDS12741.1 Transcript intron_variant - - - - - - rs11083954 19:49441366 T ENSESTG00000003527 ENSESTT00000008829 Transcript intron_variant - - - - - - rs11083954 19:49441366 T 27294 NM_014475.3 Transcript intron_variant - - - - - - rs11083954 19:49441366 T ENSESTG00000003527 ENSESTT00000008823 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010745 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010746 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010751 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010748 Transcript intron_variant - - - - - - rs2387770 19:49645911 T CCDS12758.1 CCDS12758.1 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010755 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010736 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010762 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010759 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010728 Transcript intron_variant - - - - - - rs2387770 19:49645911 T 8541 NM_003660.2 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010740 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010724 Transcript intron_variant - - - - - - rs2387770 19:49645911 T ENSESTG00000004254 ENSESTT00000010756 Transcript intron_variant - - - - - - rs1175799 19:49695824 C CCDS33073.1 CCDS33073.1 Transcript intron_variant - - - - - - rs1175799 19:49695824 C CCDS56098.1 CCDS56098.1 Transcript intron_variant - - - - - - rs1175799 19:49695824 C ENSESTG00000004396 ENSESTT00000011200 Transcript intron_variant - - - - - - rs1175799 19:49695824 C 54795 NM_001195227.1 Transcript intron_variant - - - - - - rs1175799 19:49695824 C ENSESTG00000004396 ENSESTT00000011196 Transcript intron_variant - - - - - - rs1175799 19:49695824 C 54795 NM_017636.3 Transcript intron_variant - - - - - - rs2914670 19:50003708 C - ENSR00000045151 RegulatoryFeature regulatory_region_variant - - - - - - rs2914670 19:50003708 C 6205 NM_001015.4 Transcript downstream_gene_variant - - - - - - DISTANCE=739 rs2914670 19:50003708 C 406942 NR_029703.1 Transcript downstream_gene_variant - - - - - - DISTANCE=334 rs2914670 19:50003708 C CCDS12769.1 CCDS12769.1 Transcript downstream_gene_variant - - - - - - DISTANCE=816 rs2914670 19:50003708 C ENSESTG00000004871 ENSESTT00000012357 Transcript downstream_gene_variant - - - - - - DISTANCE=762 rs2914670 19:50003708 C 84546 NR_001285.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2645 rs2914670 19:50003708 C ENSESTG00000004865 ENSESTT00000012339 Transcript downstream_gene_variant - - - - - - DISTANCE=2741 rs4429389 19:50093454 T - ENSR00000348217 RegulatoryFeature regulatory_region_variant - - - - - - rs4429389 19:50093454 T CCDS46143.1 CCDS46143.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1458 rs4429389 19:50093454 T ENSESTG00000004929 ENSESTT00000012543 Transcript intron_variant - - - - - - rs4429389 19:50093454 T ENSESTG00000004921 ENSESTT00000012515 Transcript missense_variant 79 63 21 K/N aaA/aaT - rs4429389 19:50093454 T 5639 NM_000951.2 Transcript intron_variant - - - - - - rs4429389 19:50093454 T 57479 NM_020719.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1458 rs4429389 19:50093454 T CCDS12773.1 CCDS12773.1 Transcript intron_variant - - - - - - rs4429389 19:50093454 T ENSESTG00000004929 ENSESTT00000012547 Transcript downstream_gene_variant - - - - - - DISTANCE=235 rs4429389 19:50093454 T ENSESTG00000004929 ENSESTT00000012540 Transcript intron_variant - - - - - - rs11666611 19:50214799 C 126129 NM_001136052.2 Transcript intron_variant - - - - - - rs11666611 19:50214799 C ENSESTG00000005064 ENSESTT00000012944 Transcript intron_variant - - - - - - rs11666611 19:50214799 C ENSESTG00000005064 ENSESTT00000012935 Transcript intron_variant - - - - - - rs11666611 19:50214799 C CCDS46147.1 CCDS46147.1 Transcript intron_variant - - - - - - rs11666611 19:50214799 C CCDS12779.1 CCDS12779.1 Transcript intron_variant - - - - - - rs11666611 19:50214799 C 126129 NM_152359.2 Transcript intron_variant - - - - - - rs11666611 19:50214799 C 126129 NM_001199752.1 Transcript intron_variant - - - - - - rs11666611 19:50214799 C 126129 NM_001199753.1 Transcript intron_variant - - - - - - rs11666611 19:50214799 C ENSESTG00000005064 ENSESTT00000012954 Transcript intron_variant - - - - - - rs1290654 19:50343755 G ENSESTG00000012215 ENSESTT00000030625 Transcript downstream_gene_variant - - - - - - DISTANCE=4728 rs1290654 19:50343755 G CCDS33075.1 CCDS33075.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3554 rs1290654 19:50343755 G ENSESTG00000012215 ENSESTT00000030626 Transcript downstream_gene_variant - - - - - - DISTANCE=4891 rs1290654 19:50343755 G 100506033 NR_040037.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1290654 19:50343755 G ENSESTG00000012215 ENSESTT00000030618 Transcript downstream_gene_variant - - - - - - DISTANCE=3520 rs1290654 19:50343755 G 81857 NM_030973.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3518 rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030957 Transcript missense_variant 354 350 117 D/G gAc/gGc - rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030977 Transcript upstream_gene_variant - - - - - - DISTANCE=777 rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030969 Transcript missense_variant 385 227 76 D/G gAc/gGc - rs8109661 19:50383591 G 79735 NM_001168222.1 Transcript missense_variant 451 152 51 D/G gAc/gGc - PolyPhen=benign;SIFT=tolerated rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030926 Transcript missense_variant 362 176 59 D/G gAc/gGc - rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030985 Transcript upstream_gene_variant - - - - - - DISTANCE=777 rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030890 Transcript missense_variant 362 176 59 D/G gAc/gGc - rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030974 Transcript missense_variant 385 227 76 D/G gAc/gGc - rs8109661 19:50383591 G ENSESTG00000012270 ENSESTT00000030778 Transcript downstream_gene_variant - - - - - - DISTANCE=2976 rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030912 Transcript 5_prime_UTR_variant 362 - - - - - rs8109661 19:50383591 G 84335 NM_001098632.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2947 rs8109661 19:50383591 G 84335 NM_032375.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3013 rs8109661 19:50383591 G 79735 NM_024682.2 Transcript missense_variant 550 251 84 D/G gAc/gGc - PolyPhen=benign;SIFT=tolerated rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030941 Transcript downstream_gene_variant - - - - - - DISTANCE=1432 rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030981 Transcript upstream_gene_variant - - - - - - DISTANCE=777 rs8109661 19:50383591 G ENSESTG00000012906 ENSESTT00000032370 Transcript upstream_gene_variant - - - - - - DISTANCE=1983 rs8109661 19:50383591 G CCDS54294.1 CCDS54294.1 Transcript missense_variant 152 152 51 D/G gAc/gGc - PolyPhen=benign;SIFT=tolerated rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030959 Transcript missense_variant 354 350 117 D/G gAc/gGc - rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030948 Transcript missense_variant 354 350 117 D/G gAc/gGc - rs8109661 19:50383591 G 84335 NM_001098633.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2979 rs8109661 19:50383591 G CCDS12785.1 CCDS12785.1 Transcript missense_variant 251 251 84 D/G gAc/gGc - PolyPhen=benign;SIFT=tolerated rs8109661 19:50383591 G ENSESTG00000012289 ENSESTT00000030973 Transcript 5_prime_UTR_variant 385 - - - - - rs283538 19:50444028 C ENSESTG00000012874 ENSESTT00000032279 Transcript intron_variant - - - - - - rs7253507 19:50997140 C - - - intergenic_variant - - - - - - rs198960 19:51387108 G ENSESTG00000019211 ENSESTT00000048379 Transcript downstream_gene_variant - - - - - - DISTANCE=4623 rs198960 19:51387108 G 3817 NM_005551.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3285 rs198960 19:51387108 G 3817 NR_045762.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3285 rs198960 19:51387108 G 3817 NM_001256080.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3285 rs198960 19:51387108 G 606293 NR_002948.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs198960 19:51387108 G 3817 NR_045763.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3285 rs198960 19:51387108 G 3817 NM_001002231.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3285 rs183854 19:51452250 C ENSESTG00000020149 ENSESTT00000050597 Transcript missense_variant 557 457 153 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs183854 19:51452250 C 25818 NM_001077492.1 Transcript missense_variant 607 457 153 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs183854 19:51452250 C 25818 NM_012427.4 Transcript missense_variant 810 457 153 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs183854 19:51452250 C 25818 NM_001077491.1 Transcript missense_variant 675 457 153 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs183854 19:51452250 C ENSESTG00000020149 ENSESTT00000050583 Transcript missense_variant 612 457 153 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs183854 19:51452250 C CCDS12810.1 CCDS12810.1 Transcript missense_variant 457 457 153 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs9304709 19:51720630 A - - - intergenic_variant - - - - - - rs169274 19:51794976 G - - - intergenic_variant - - - - - - rs273626 19:51805918 T - - - intergenic_variant - - - - - - rs1870070 19:52041291 G - - - intergenic_variant - - - - - - rs4802832 19:52142264 A CCDS42604.1 CCDS42604.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4344 rs4802832 19:52142264 A ENSESTG00000019802 ENSESTT00000049634 Transcript intron_variant - - - - - - rs4802832 19:52142264 A ENSESTG00000019761 ENSESTT00000049591 Transcript intron_variant - - - - - - rs4802832 19:52142264 A 100049587 NM_001098612.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3542 rs4802832 19:52142264 A ENSESTG00000019761 ENSESTT00000049612 Transcript intron_variant - - - - - - rs12975313 19:52539641 A 9668 NM_014650.2 Transcript intron_variant - - - - - - rs12975313 19:52539641 A CCDS12848.1 CCDS12848.1 Transcript intron_variant - - - - - - rs2560872 19:52777213 T CCDS46163.1 CCDS46163.1 Transcript intron_variant - - - - - - rs2560872 19:52777213 T 90321 NM_001010851.2 Transcript intron_variant - - - - - - rs35980658 19:53229150 G - ENSR00000348629 RegulatoryFeature regulatory_region_variant - - - - - - rs35980658 19:53229150 G 81856 NM_030972.3 Transcript intron_variant - - - - - - rs35980658 19:53229150 G 81856 NM_001161500.1 Transcript intron_variant - - - - - - rs35980658 19:53229150 G 81856 NM_001161499.1 Transcript intron_variant - - - - - - rs35980658 19:53229150 G 81856 NM_001161501.1 Transcript intron_variant - - - - - - rs10404813 19:53245076 C - - - intergenic_variant - - - - - - rs1833816 19:53249334 G - - - intergenic_variant - - - - - - rs11084195 19:53309177 G CCDS33093.2 CCDS33093.2 Transcript intron_variant - - - - - - rs11084195 19:53309177 G 7576 NR_036600.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11084195 19:53309177 G 7576 NM_006969.3 Transcript intron_variant - - - - - - rs11084195 19:53309177 G 7576 NR_036599.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1560100 19:53562239 A - - - intergenic_variant - - - - - - rs379195 19:54765958 G CCDS46176.1 CCDS46176.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4902 rs379195 19:54765958 G 10990 NM_006840.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4791 rs379195 19:54765958 G ENSESTG00000035017 ENSESTT00000088509 Transcript upstream_gene_variant - - - - - - DISTANCE=4821 rs379195 19:54765958 G 10990 NM_001081443.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4791 rs379195 19:54765958 G ENSESTG00000035017 ENSESTT00000088514 Transcript upstream_gene_variant - - - - - - DISTANCE=4824 rs379195 19:54765958 G CCDS12885.1 CCDS12885.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4902 rs379195 19:54765958 G 10990 NM_001081442.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4791 rs379195 19:54765958 G CCDS42611.1 CCDS42611.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4902 rs10405795 19:55004169 G - - - intergenic_variant - - - - - - rs413679 19:55173806 G - ENSR00000348892 RegulatoryFeature regulatory_region_variant - - - - - - rs413679 19:55173806 G CCDS12902.1 CCDS12902.1 Transcript upstream_gene_variant - - - - - - DISTANCE=680 rs413679 19:55173806 G 11006 NM_001081438.1 Transcript upstream_gene_variant - - - - - - DISTANCE=318 rs413679 19:55173806 G CCDS42618.1 CCDS42618.1 Transcript upstream_gene_variant - - - - - - DISTANCE=680 rs413679 19:55173806 G ENSESTG00000034957 ENSESTT00000088358 Transcript upstream_gene_variant - - - - - - DISTANCE=632 rs413679 19:55173806 G ENSESTG00000034957 ENSESTT00000088366 Transcript upstream_gene_variant - - - - - - DISTANCE=650 rs413679 19:55173806 G 11006 NM_006847.3 Transcript upstream_gene_variant - - - - - - DISTANCE=318 rs2099355 19:55269292 G 3804 NM_015868.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4788 rs2099355 19:55269292 G ENSESTG00000008102 ENSESTT00000020489 Transcript intron_variant - - - - - - rs2099355 19:55269292 G ENSESTG00000008102 ENSESTT00000020507 Transcript intron_variant - - - - - - rs4806442 19:55273135 T ENSESTG00000008102 ENSESTT00000020489 Transcript intron_variant - - - - - - rs4806442 19:55273135 T ENSESTG00000008102 ENSESTT00000020507 Transcript intron_variant - - - - - - rs890872 19:55671337 T ENSESTG00000009231 ENSESTT00000023153 Transcript downstream_gene_variant - - - - - - DISTANCE=2278 rs890872 19:55671337 T 352909 NM_001256716.1 Transcript missense_variant 1384 931 311 D/N Gat/Aat - PolyPhen=benign;SIFT=tolerated rs890872 19:55671337 T CCDS58680.1 CCDS58680.1 Transcript missense_variant 1294 1294 432 D/N Gat/Aat - PolyPhen=benign;SIFT=tolerated rs890872 19:55671337 T 352909 NM_001256715.1 Transcript missense_variant 1297 1093 365 D/N Gat/Aat - PolyPhen=benign;SIFT=tolerated rs890872 19:55671337 T ENSESTG00000009245 ENSESTT00000023208 Transcript upstream_gene_variant - - - - - - DISTANCE=3244 rs890872 19:55671337 T 352909 NM_178837.4 Transcript missense_variant 1308 1234 412 D/N Gat/Aat - PolyPhen=benign;SIFT=tolerated rs890872 19:55671337 T ENSESTG00000009231 ENSESTT00000023166 Transcript downstream_gene_variant - - - - - - DISTANCE=2293 rs890872 19:55671337 T 7137 NM_000363.4 Transcript upstream_gene_variant - - - - - - DISTANCE=2237 rs890872 19:55671337 T CCDS42628.1 CCDS42628.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2380 rs890872 19:55671337 T CCDS12918.2 CCDS12918.2 Transcript missense_variant 1234 1234 412 D/N Gat/Aat - PolyPhen=benign;SIFT=tolerated rs890872 19:55671337 T 352909 NM_001256714.1 Transcript missense_variant 1368 1294 432 D/N Gat/Aat - PolyPhen=benign;SIFT=tolerated rs890872 19:55671337 T ENSESTG00000009231 ENSESTT00000023163 Transcript downstream_gene_variant - - - - - - DISTANCE=2253 rs890872 19:55671337 T CCDS58679.1 CCDS58679.1 Transcript missense_variant 931 931 311 D/N Gat/Aat - PolyPhen=benign;SIFT=tolerated rs890870 19:55699454 C 5794 NM_002842.3 Transcript missense_variant 2540 2467 823 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs890870 19:55699454 C ENSESTG00000009191 ENSESTT00000023044 Transcript synonymous_variant 132 33 11 T acA/acG - rs890870 19:55699454 C ENSESTG00000009191 ENSESTT00000023038 Transcript missense_variant,splice_region_variant 363 256 86 K/E Aag/Gag - rs890870 19:55699454 C CCDS33110.1 CCDS33110.1 Transcript missense_variant 2467 2467 823 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs890870 19:55699454 C 5794 NM_001161440.1 Transcript missense_variant 2006 1933 645 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs890870 19:55699454 C ENSESTG00000009195 ENSESTT00000023054 Transcript upstream_gene_variant - - - - - - DISTANCE=2553 rs890870 19:55699454 C CCDS54321.1 CCDS54321.1 Transcript missense_variant 1933 1933 645 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs890870 19:55699454 C ENSESTG00000009191 ENSESTT00000023030 Transcript missense_variant 435 256 86 K/E Aag/Gag - rs11882203 19:56014631 T - ENSR00000642049 RegulatoryFeature regulatory_region_variant - - - - - - rs11882203 19:56014631 T CCDS46196.1 CCDS46196.1 Transcript intron_variant - - - - - - rs11882203 19:56014631 T ENSESTG00000008879 ENSESTT00000022271 Transcript intron_variant - - - - - - rs11882203 19:56014631 T 284297 NM_001144950.1 Transcript intron_variant - - - - - - rs11882203 19:56014631 T ENSESTG00000008869 ENSESTT00000022256 Transcript downstream_gene_variant - - - - - - DISTANCE=3257 rs11882203 19:56014631 T ENSESTG00000008869 ENSESTT00000022253 Transcript downstream_gene_variant - - - - - - DISTANCE=3285 rs11882203 19:56014631 T 284297 NM_001195267.1 Transcript intron_variant - - - - - - rs11882203 19:56014631 T ENSESTG00000008879 ENSESTT00000022268 Transcript intron_variant - - - - - - rs602335 19:56077594 C - - - intergenic_variant - - - - - - rs193384 19:56241265 G CCDS12934.1 CCDS12934.1 Transcript synonymous_variant 1926 1926 642 L ctT/ctC - rs193384 19:56241265 G 338321 NM_176820.2 Transcript synonymous_variant 1954 1926 642 L ctT/ctC - rs299162 19:56242644 C CCDS12934.1 CCDS12934.1 Transcript intron_variant - - - - - - rs299162 19:56242644 C 338321 NM_176820.2 Transcript intron_variant - - - - - - rs306486 19:56483446 C CCDS12937.1 CCDS12937.1 Transcript intron_variant - - - - - - rs306486 19:56483446 C 126205 NM_176811.2 Transcript intron_variant - - - - - - rs274174 19:56693643 C ENSESTG00000030705 ENSESTT00000077288 Transcript downstream_gene_variant - - - - - - DISTANCE=24 rs274174 19:56693643 C 85569 NM_033106.3 Transcript intron_variant - - - - - - rs274174 19:56693643 C 85569 NM_001145546.1 Transcript intron_variant - - - - - - rs274174 19:56693643 C CCDS46202.1 CCDS46202.1 Transcript downstream_gene_variant - - - - - - DISTANCE=40 rs274174 19:56693643 C CCDS12940.1 CCDS12940.1 Transcript intron_variant - - - - - - rs726305 19:56795370 G ENSESTG00000030709 ENSESTT00000077297 Transcript upstream_gene_variant - - - - - - DISTANCE=143 rs4801164 19:56997767 T 100128252 NR_036522.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4801164 19:56997767 T 100128252 NR_036521.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1158031 19:57218515 G - - - intergenic_variant - - - - - - rs11882764 19:57246907 A - - - intergenic_variant - - - - - - rs4801465 19:57834897 C CCDS33130.1 CCDS33130.1 Transcript intron_variant - - - - - - rs4801465 19:57834897 C ENSESTG00000002921 ENSESTT00000007277 Transcript intron_variant - - - - - - rs4801465 19:57834897 C 125919 NM_213598.3 Transcript intron_variant - - - - - - rs4801499 19:58033427 A - - - intergenic_variant - - - - - - rs7259128 19:58092295 A ENSESTG00000003016 ENSESTT00000007505 Transcript upstream_gene_variant - - - - - - DISTANCE=2715 rs7259128 19:58092295 A 284307 NM_001010879.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3333 rs7259128 19:58092295 A ENSESTG00000003016 ENSESTT00000007496 Transcript intron_variant - - - - - - rs7259128 19:58092295 A CCDS12954.1 CCDS12954.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2223 rs7259128 19:58092295 A ENSESTG00000003016 ENSESTT00000007508 Transcript upstream_gene_variant - - - - - - DISTANCE=2715 rs7259128 19:58092295 A CCDS33135.1 CCDS33135.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3430 rs7259128 19:58092295 A ENSESTG00000003016 ENSESTT00000007518 Transcript upstream_gene_variant - - - - - - DISTANCE=4022 rs7259128 19:58092295 A ENSESTG00000003016 ENSESTT00000007512 Transcript upstream_gene_variant - - - - - - DISTANCE=2715 rs7259128 19:58092295 A 55659 NM_017879.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2052 rs10423430 19:58449398 T ENSESTG00000035749 ENSESTT00000090324 Transcript downstream_gene_variant - - - - - - DISTANCE=4286 rs10423430 19:58449398 T CCDS12966.1 CCDS12966.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2894 rs10423430 19:58449398 T ENSESTG00000035750 ENSESTT00000090327 Transcript upstream_gene_variant - - - - - - DISTANCE=2650 rs10423430 19:58449398 T ENSESTG00000035749 ENSESTT00000090323 Transcript downstream_gene_variant - - - - - - DISTANCE=4384 rs10423430 19:58449398 T ENSESTG00000035750 ENSESTT00000090328 Transcript upstream_gene_variant - - - - - - DISTANCE=2650 rs10423430 19:58449398 T ENSESTG00000035750 ENSESTT00000090329 Transcript upstream_gene_variant - - - - - - DISTANCE=2657 rs10423430 19:58449398 T 10172 NM_005773.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2803 rs10423430 19:58449398 T CCDS42642.1 CCDS42642.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4208 rs10423430 19:58449398 T ENSESTG00000035750 ENSESTT00000090326 Transcript upstream_gene_variant - - - - - - DISTANCE=2647 rs10423430 19:58449398 T 147686 NM_133460.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2658 rs10423430 19:58449398 T ENSESTG00000035750 ENSESTT00000090325 Transcript upstream_gene_variant - - - - - - DISTANCE=2637 rs10423430 19:58449398 T ENSESTG00000035750 ENSESTT00000090330 Transcript upstream_gene_variant - - - - - - DISTANCE=3793 rs483303 19:58711998 A 10782 NM_016324.2 Transcript intron_variant - - - - - - rs483303 19:58711998 A ENSESTG00000035714 ENSESTT00000090238 Transcript intron_variant - - - - - - rs483303 19:58711998 A ENSESTG00000035714 ENSESTT00000090237 Transcript intron_variant - - - - - - rs483303 19:58711998 A 10782 NM_016325.2 Transcript intron_variant - - - - - - rs483303 19:58711998 A ENSESTG00000035714 ENSESTT00000090236 Transcript intron_variant - - - - - - rs483303 19:58711998 A ENSESTG00000035714 ENSESTT00000090239 Transcript intron_variant - - - - - - rs483303 19:58711998 A 10782 NM_133502.1 Transcript intron_variant - - - - - - rs1265985 19:58830467 A - ENSR00000349279 RegulatoryFeature regulatory_region_variant - - - - - - rs1265985 19:58830467 A - - - intergenic_variant - - - - - - rs6051521 20:352164 G - ENSR00000396292 RegulatoryFeature regulatory_region_variant - - - - - - rs6051521 20:352164 G ENSESTG00000016785 ENSESTT00000042137 Transcript intron_variant - - - - - - rs805886 20:811430 G ENSESTG00000016924 ENSESTT00000042472 Transcript upstream_gene_variant - - - - - - DISTANCE=2990 rs805886 20:811430 G 83541 NM_001042353.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2926 rs805886 20:811430 G ENSESTG00000016924 ENSESTT00000042466 Transcript upstream_gene_variant - - - - - - DISTANCE=2926 rs537795 20:876420 C CCDS13009.1 CCDS13009.1 Transcript intron_variant - - - - - - rs537795 20:876420 C ENSESTG00000016947 ENSESTT00000042491 Transcript intron_variant - - - - - - rs537795 20:876420 C 51378 NM_015985.2 Transcript intron_variant - - - - - - rs542943 20:883923 T CCDS13009.1 CCDS13009.1 Transcript intron_variant - - - - - - rs542943 20:883923 T ENSESTG00000016947 ENSESTT00000042491 Transcript intron_variant - - - - - - rs542943 20:883923 T 51378 NM_015985.2 Transcript intron_variant - - - - - - rs4813963 20:1171502 A - ENSR00000233306 RegulatoryFeature regulatory_region_variant - - - - - - rs4813963 20:1171502 A ENSESTG00000005143 ENSESTT00000013031 Transcript intron_variant - - - - - - rs4814135 20:1308706 G - ENSR00000007860 RegulatoryFeature regulatory_region_variant - - - - - - rs4814135 20:1308706 G ENSESTG00000005162 ENSESTT00000013108 Transcript intron_variant - - - - - - rs4814135 20:1308706 G 100507495 NR_040048.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4814135 20:1308706 G ENSESTG00000005269 ENSESTT00000013513 Transcript intron_variant - - - - - - rs4814135 20:1308706 G 100528031 NR_037661.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4814135 20:1308706 G 27111 NM_001199784.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2193 rs4814135 20:1308706 G ENSESTG00000005269 ENSESTT00000013512 Transcript intron_variant - - - - - - rs4814135 20:1308706 G ENSESTG00000005269 ENSESTT00000013482 Transcript intron_variant - - - - - - rs4814135 20:1308706 G ENSESTG00000005269 ENSESTT00000013494 Transcript intron_variant - - - - - - rs4814135 20:1308706 G 100507495 NR_040047.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4814135 20:1308706 G 100507495 NR_040049.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4814135 20:1308706 G 27111 NM_080489.4 Transcript intron_variant - - - - - - rs4814135 20:1308706 G ENSESTG00000005269 ENSESTT00000013428 Transcript intron_variant - - - - - - rs376197 20:1370820 C 100528031 NR_037661.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs376197 20:1370820 C 2280 NM_000801.4 Transcript intron_variant - - - - - - rs376197 20:1370820 C ENSESTG00000005269 ENSESTT00000013469 Transcript intron_variant - - - - - - rs376197 20:1370820 C ENSESTG00000005269 ENSESTT00000013473 Transcript intron_variant - - - - - - rs376197 20:1370820 C 2280 NM_001199786.1 Transcript intron_variant - - - - - - rs376197 20:1370820 C ENSESTG00000005269 ENSESTT00000013428 Transcript intron_variant - - - - - - rs376197 20:1370820 C CCDS13014.1 CCDS13014.1 Transcript intron_variant - - - - - - rs376197 20:1370820 C 2280 NM_054014.3 Transcript intron_variant - - - - - - rs6042199 20:1404549 C - ENSR00000396452 RegulatoryFeature regulatory_region_variant - - - - - - rs6042199 20:1404549 C - - - intergenic_variant - - - - - - rs562527 20:1728159 G - - - intergenic_variant - - - - - - rs6047478 20:2207442 T - - - intergenic_variant - - - - - - rs4346458 20:2246240 A - - - intergenic_variant - - - - - - rs6051618 20:3158821 T - - - intergenic_variant - - - - - - rs6051619 20:3158907 G - ENSR00000233390 RegulatoryFeature regulatory_region_variant - - - - - - rs6051619 20:3158907 G - - - intergenic_variant - - - - - - rs239481 20:3382175 A ENSESTG00000003269 ENSESTT00000008151 Transcript intron_variant - - - - - - rs239481 20:3382175 A 25943 NM_001009984.2 Transcript intron_variant - - - - - - rs239481 20:3382175 A ENSESTG00000003269 ENSESTT00000008135 Transcript intron_variant - - - - - - rs239481 20:3382175 A CCDS42851.1 CCDS42851.1 Transcript intron_variant - - - - - - rs4815622 20:3879248 T ENSESTG00000003216 ENSESTT00000007998 Transcript intron_variant - - - - - - rs4815622 20:3879248 T 80025 NM_153640.2 Transcript intron_variant - - - - - - rs4815622 20:3879248 T ENSESTG00000003216 ENSESTT00000008032 Transcript intron_variant - - - - - - rs4815622 20:3879248 T CCDS13071.2 CCDS13071.2 Transcript intron_variant - - - - - - rs4815622 20:3879248 T 80025 NM_024960.4 Transcript intron_variant - - - - - - rs4815622 20:3879248 T 80025 NM_153638.2 Transcript intron_variant - - - - - - rs297674 20:4442770 A - - - intergenic_variant - - - - - - rs297649 20:4445533 T - - - intergenic_variant - - - - - - rs856884 20:4462731 A - ENSR00000396920 RegulatoryFeature regulatory_region_variant - - - - - - rs856884 20:4462731 A - - - intergenic_variant - - - - - - rs6052604 20:4493659 A - ENSR00001446765 RegulatoryFeature regulatory_region_variant - - - - - - rs6052604 20:4493659 A - - - intergenic_variant - - - - - - rs182433 20:4505160 A - - - intergenic_variant - - - - - - rs2038434 20:4506425 T - - - intergenic_variant - - - - - - rs2038435 20:4506537 A - - - intergenic_variant - - - - - - rs2093093 20:4509550 A - - - intergenic_variant - - - - - - rs4239764 20:5299823 T ENSESTG00000003876 ENSESTT00000009746 Transcript upstream_gene_variant - - - - - - DISTANCE=2445 rs4239764 20:5299823 T 128674 NM_144773.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4808 rs4239764 20:5299823 T CCDS13089.1 CCDS13089.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4808 rs6053311 20:5305389 C - - - intergenic_variant - - - - - - rs6038163 20:5398043 A - - - intergenic_variant - - - - - - rs370819 20:5914953 T CCDS13093.1 CCDS13093.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4228 rs370819 20:5914953 T 51605 NM_015939.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3533 rs236100 20:5948706 G 84515 NM_182802.1 Transcript intron_variant - - - - - - rs236100 20:5948706 G CCDS13094.1 CCDS13094.1 Transcript intron_variant - - - - - - rs236100 20:5948706 G 84515 NM_032485.4 Transcript intron_variant - - - - - - rs236100 20:5948706 G ENSESTG00000030069 ENSESTT00000075798 Transcript upstream_gene_variant - - - - - - DISTANCE=4991 rs236100 20:5948706 G CCDS13095.1 CCDS13095.1 Transcript intron_variant - - - - - - rs236101 20:5948712 T 84515 NM_182802.1 Transcript intron_variant - - - - - - rs236101 20:5948712 T CCDS13094.1 CCDS13094.1 Transcript intron_variant - - - - - - rs236101 20:5948712 T 84515 NM_032485.4 Transcript intron_variant - - - - - - rs236101 20:5948712 T ENSESTG00000030069 ENSESTT00000075798 Transcript upstream_gene_variant - - - - - - DISTANCE=4985 rs236101 20:5948712 T CCDS13095.1 CCDS13095.1 Transcript intron_variant - - - - - - rs6076907 20:5985365 C CCDS46578.1 CCDS46578.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2683 rs6076907 20:5985365 C CCDS13096.1 CCDS13096.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1528 rs6076907 20:5985365 C ENSESTG00000030148 ENSESTT00000075898 Transcript upstream_gene_variant - - - - - - DISTANCE=1534 rs6076907 20:5985365 C 54675 NM_019095.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1374 rs6076907 20:5985365 C 54675 NM_001127458.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2533 rs2423132 20:6011882 T CCDS46578.1 CCDS46578.1 Transcript intron_variant - - - - - - rs2423132 20:6011882 T CCDS13096.1 CCDS13096.1 Transcript intron_variant - - - - - - rs2423132 20:6011882 T ENSESTG00000030169 ENSESTT00000076034 Transcript intron_variant - - - - - - rs2423132 20:6011882 T ENSESTG00000030169 ENSESTT00000076020 Transcript intron_variant - - - - - - rs2423132 20:6011882 T 54675 NM_019095.4 Transcript intron_variant - - - - - - rs2423132 20:6011882 T 54675 NM_001127458.1 Transcript intron_variant - - - - - - rs6054436 20:6644177 A - ENSR00000397225 RegulatoryFeature regulatory_region_variant - - - - - - rs6054436 20:6644177 A - - - intergenic_variant - - - - - - rs2423168 20:6890635 A - ENSR00001446924 RegulatoryFeature regulatory_region_variant - - - - - - rs2423168 20:6890635 A - - - intergenic_variant - - - - - - rs1159617 20:7213705 A - ENSR00000397304 RegulatoryFeature regulatory_region_variant - - - - - - rs1159617 20:7213705 A - - - intergenic_variant - - - - - - rs6077190 20:7321038 C - - - intergenic_variant - - - - - - rs2207714 20:7500645 G - - - intergenic_variant - - - - - - rs6038866 20:7522770 A - - - intergenic_variant - - - - - - rs6055136 20:7562488 G - - - intergenic_variant - - - - - - rs2206460 20:7822580 G - ENSR00000397354 RegulatoryFeature regulatory_region_variant - - - - - - rs2206460 20:7822580 G - - - intergenic_variant - - - - - - rs2205816 20:7909051 T ENSESTG00000011930 ENSESTT00000029905 Transcript intron_variant - - - - - - rs2205816 20:7909051 T 54363 NM_017545.2 Transcript intron_variant - - - - - - rs2205816 20:7909051 T CCDS13100.1 CCDS13100.1 Transcript intron_variant - - - - - - rs6118117 20:8192387 A 23236 NM_015192.2 Transcript intron_variant - - - - - - rs6118117 20:8192387 A CCDS13103.1 CCDS13103.1 Transcript intron_variant - - - - - - rs6118117 20:8192387 A 23236 NM_182734.1 Transcript intron_variant - - - - - - rs6118117 20:8192387 A CCDS13102.1 CCDS13102.1 Transcript intron_variant - - - - - - rs6039097 20:8195617 A 23236 NM_015192.2 Transcript intron_variant - - - - - - rs6039097 20:8195617 A CCDS13103.1 CCDS13103.1 Transcript intron_variant - - - - - - rs6039097 20:8195617 A 23236 NM_182734.1 Transcript intron_variant - - - - - - rs6039097 20:8195617 A CCDS13102.1 CCDS13102.1 Transcript intron_variant - - - - - - rs2719788 20:8265656 T 23236 NM_015192.2 Transcript intron_variant - - - - - - rs2719788 20:8265656 T CCDS13103.1 CCDS13103.1 Transcript intron_variant - - - - - - rs2719788 20:8265656 T 23236 NM_182734.1 Transcript intron_variant - - - - - - rs2719788 20:8265656 T CCDS13102.1 CCDS13102.1 Transcript intron_variant - - - - - - rs6039171 20:8459568 G 23236 NM_015192.2 Transcript intron_variant - - - - - - rs6039171 20:8459568 G CCDS13103.1 CCDS13103.1 Transcript intron_variant - - - - - - rs6039171 20:8459568 G 23236 NM_182734.1 Transcript intron_variant - - - - - - rs6039171 20:8459568 G CCDS13102.1 CCDS13102.1 Transcript intron_variant - - - - - - rs2179979 20:8688309 A 23236 NM_015192.2 Transcript intron_variant - - - - - - rs2179979 20:8688309 A CCDS13103.1 CCDS13103.1 Transcript intron_variant - - - - - - rs2179979 20:8688309 A 23236 NM_182734.1 Transcript intron_variant - - - - - - rs2179979 20:8688309 A CCDS13102.1 CCDS13102.1 Transcript intron_variant - - - - - - rs2179979 20:8688309 A ENSESTG00000011902 ENSESTT00000029808 Transcript intron_variant - - - - - - rs1534929 20:9288116 G ENSESTG00000011875 ENSESTT00000029827 Transcript intron_variant - - - - - - rs1534929 20:9288116 G 5332 NM_001172646.1 Transcript intron_variant - - - - - - rs1534929 20:9288116 G CCDS54447.1 CCDS54447.1 Transcript upstream_gene_variant - - - - - - DISTANCE=346 rs1534929 20:9288116 G ENSESTG00000011875 ENSESTT00000029829 Transcript intron_variant - - - - - - rs1534929 20:9288116 G ENSESTG00000011875 ENSESTT00000029820 Transcript intron_variant - - - - - - rs1534929 20:9288116 G 5332 NM_182797.2 Transcript intron_variant - - - - - - rs1534929 20:9288116 G CCDS13105.1 CCDS13105.1 Transcript upstream_gene_variant - - - - - - DISTANCE=346 rs1534929 20:9288116 G ENSESTG00000011875 ENSESTT00000029836 Transcript intron_variant - - - - - - rs1534929 20:9288116 G ENSESTG00000011875 ENSESTT00000029819 Transcript intron_variant - - - - - - rs1534929 20:9288116 G ENSESTG00000011875 ENSESTT00000029833 Transcript intron_variant - - - - - - rs1534929 20:9288116 G CCDS13104.1 CCDS13104.1 Transcript upstream_gene_variant - - - - - - DISTANCE=346 rs1534929 20:9288116 G 5332 NM_000933.3 Transcript upstream_gene_variant - - - - - - DISTANCE=331 rs6133727 20:9570942 G - ENSR00001021754 RegulatoryFeature regulatory_region_variant - - - - - - rs6133727 20:9570942 G CCDS13107.1 CCDS13107.1 Transcript intron_variant - - - - - - rs6133727 20:9570942 G 57144 NM_177990.2 Transcript intron_variant - - - - - - rs6133727 20:9570942 G ENSESTG00000011933 ENSESTT00000029915 Transcript intron_variant - - - - - - rs6133727 20:9570942 G 57144 NM_020341.3 Transcript intron_variant - - - - - - rs4142355 20:9644902 A 57144 NM_177990.2 Transcript intron_variant - - - - - - rs4142355 20:9644902 A ENSESTG00000011933 ENSESTT00000029915 Transcript intron_variant - - - - - - rs4142355 20:9644902 A ENSESTG00000011933 ENSESTT00000029908 Transcript intron_variant - - - - - - rs4142355 20:9644902 A 57144 NM_020341.3 Transcript intron_variant - - - - - - rs2423424 20:9684667 C 57144 NM_177990.2 Transcript intron_variant - - - - - - rs2423424 20:9684667 C ENSESTG00000011933 ENSESTT00000029915 Transcript intron_variant - - - - - - rs2423424 20:9684667 C ENSESTG00000011933 ENSESTT00000029908 Transcript intron_variant - - - - - - rs2423424 20:9684667 C 57144 NM_020341.3 Transcript intron_variant - - - - - - rs4816202 20:9995402 C - - - intergenic_variant - - - - - - rs2423493 20:10335863 T - - - intergenic_variant - - - - - - rs221665 20:10405970 A 8195 NR_072977.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs221665 20:10405970 A ENSESTG00000025761 ENSESTT00000065029 Transcript intron_variant - - - - - - rs221665 20:10405970 A ENSESTG00000025761 ENSESTT00000064977 Transcript intron_variant - - - - - - rs221665 20:10405970 A 8195 NM_018848.3 Transcript intron_variant - - - - - - rs221665 20:10405970 A 8195 NM_170784.2 Transcript intron_variant - - - - - - rs4295076 20:10431354 C ENSESTG00000025679 ENSESTT00000064846 Transcript intron_variant - - - - - - rs4295076 20:10431354 C 128710 NM_001009608.1 Transcript intron_variant - - - - - - rs1327236 20:10969372 A - - - intergenic_variant - - - - - - rs2207413 20:11177356 G - - - intergenic_variant - - - - - - rs55896006 20:11259080 T - - - intergenic_variant - - - - - - rs2143869 20:11324894 C - - - intergenic_variant - - - - - - rs2809598 20:11755511 A - - - intergenic_variant - - - - - - rs1997808 20:11881024 T ENSESTG00000014844 ENSESTT00000037162 Transcript downstream_gene_variant - - - - - - DISTANCE=4186 rs1997808 20:11881024 T 22903 NM_181443.1 Transcript intron_variant - - - - - - rs1997808 20:11881024 T ENSESTG00000014823 ENSESTT00000037130 Transcript intron_variant - - - - - - rs2179682 20:11942033 A - - - intergenic_variant - - - - - - rs761797 20:12414489 G - ENSR00001447385 RegulatoryFeature regulatory_region_variant - - - - - - rs761797 20:12414489 G ENSESTG00000014856 ENSESTT00000037190 Transcript intron_variant - - - - - - rs474111 20:12544330 A - - - intergenic_variant - - - - - - rs112671 20:12617992 A ENSESTG00000014849 ENSESTT00000037177 Transcript intron_variant - - - - - - rs845596 20:12803582 G - - - intergenic_variant - - - - - - rs1011021 20:12858976 T - - - intergenic_variant - - - - - - rs6041868 20:13089932 G ENSESTG00000010524 ENSESTT00000026351 Transcript intron_variant - - - - - - rs6041868 20:13089932 G ENSESTG00000010524 ENSESTT00000026348 Transcript intron_variant - - - - - - rs6041868 20:13089932 G 55304 NM_018327.2 Transcript intron_variant - - - - - - rs6041868 20:13089932 G CCDS13115.2 CCDS13115.2 Transcript intron_variant - - - - - - rs761848 20:13124226 G ENSESTG00000010524 ENSESTT00000026348 Transcript intron_variant - - - - - - rs761848 20:13124226 G 55304 NM_018327.2 Transcript intron_variant - - - - - - rs761848 20:13124226 G CCDS13115.2 CCDS13115.2 Transcript intron_variant - - - - - - rs665965 20:13288898 A - - - intergenic_variant - - - - - - rs6033812 20:13723332 A CCDS13117.1 CCDS13117.1 Transcript intron_variant - - - - - - rs6033812 20:13723332 A 51575 NM_016649.3 Transcript intron_variant - - - - - - rs6033812 20:13723332 A ENSESTG00000010593 ENSESTT00000026519 Transcript intron_variant - - - - - - rs6079574 20:14802943 T CCDS13120.2 CCDS13120.2 Transcript intron_variant - - - - - - rs6079574 20:14802943 T 140733 NM_080676.5 Transcript intron_variant - - - - - - rs6079574 20:14802943 T ENSESTG00000025972 ENSESTT00000065458 Transcript intron_variant - - - - - - rs6079574 20:14802943 T ENSESTG00000025972 ENSESTT00000065450 Transcript intron_variant - - - - - - rs6034061 20:14897484 T CCDS13120.2 CCDS13120.2 Transcript intron_variant - - - - - - rs6034061 20:14897484 T 140733 NM_080676.5 Transcript intron_variant - - - - - - rs6034061 20:14897484 T 100379174 NR_037841.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs6034061 20:14897484 T 100379174 NR_072988.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2193281 20:15364827 C CCDS13120.2 CCDS13120.2 Transcript intron_variant - - - - - - rs2193281 20:15364827 C 140733 NM_080676.5 Transcript intron_variant - - - - - - rs2193281 20:15364827 C 140733 NM_001033087.1 Transcript intron_variant - - - - - - rs427528 20:15391011 C CCDS13120.2 CCDS13120.2 Transcript intron_variant - - - - - - rs427528 20:15391011 C 140733 NM_080676.5 Transcript intron_variant - - - - - - rs427528 20:15391011 C 140733 NM_001033087.1 Transcript intron_variant - - - - - - rs200779 20:15578210 C CCDS13120.2 CCDS13120.2 Transcript intron_variant - - - - - - rs200779 20:15578210 C 140733 NM_080676.5 Transcript intron_variant - - - - - - rs200779 20:15578210 C 140733 NM_001033087.1 Transcript intron_variant - - - - - - rs200769 20:15614458 A CCDS13120.2 CCDS13120.2 Transcript intron_variant - - - - - - rs200769 20:15614458 A 140733 NM_080676.5 Transcript intron_variant - - - - - - rs200769 20:15614458 A 140733 NM_001033087.1 Transcript intron_variant - - - - - - rs200770 20:15615555 C CCDS13120.2 CCDS13120.2 Transcript intron_variant - - - - - - rs200770 20:15615555 C 140733 NM_080676.5 Transcript intron_variant - - - - - - rs200770 20:15615555 C 140733 NM_001033087.1 Transcript intron_variant - - - - - - rs148998047 20:16238642 C - - - intergenic_variant - - - - - - rs117440222 20:16238749 C - - - intergenic_variant - - - - - - rs6080231 20:16320362 T ENSESTG00000001861 ENSESTT00000004644 Transcript intron_variant - - - - - - rs6080231 20:16320362 T ENSESTG00000001861 ENSESTT00000004637 Transcript intron_variant - - - - - - rs6080231 20:16320362 T CCDS13122.1 CCDS13122.1 Transcript intron_variant - - - - - - rs6080231 20:16320362 T ENSESTG00000001861 ENSESTT00000004650 Transcript intron_variant - - - - - - rs6080231 20:16320362 T ENSESTG00000001861 ENSESTT00000004635 Transcript intron_variant - - - - - - rs6080231 20:16320362 T 55614 NM_001199865.1 Transcript intron_variant - - - - - - rs6080231 20:16320362 T ENSESTG00000001861 ENSESTT00000004639 Transcript intron_variant - - - - - - rs6080231 20:16320362 T 55614 NM_024704.4 Transcript intron_variant - - - - - - rs6080231 20:16320362 T ENSESTG00000001861 ENSESTT00000004640 Transcript intron_variant - - - - - - rs1884599 20:16371967 C ENSESTG00000001810 ENSESTT00000004521 Transcript intron_variant - - - - - - rs1884599 20:16371967 C ENSESTG00000001810 ENSESTT00000004493 Transcript intron_variant - - - - - - rs1884599 20:16371967 C ENSESTG00000001810 ENSESTT00000004492 Transcript intron_variant - - - - - - rs1884599 20:16371967 C ENSESTG00000001810 ENSESTT00000004489 Transcript intron_variant - - - - - - rs1884599 20:16371967 C 55614 NM_001199866.1 Transcript intron_variant - - - - - - rs1884599 20:16371967 C CCDS13122.1 CCDS13122.1 Transcript intron_variant - - - - - - rs1884599 20:16371967 C ENSESTG00000001810 ENSESTT00000004525 Transcript intron_variant - - - - - - rs1884599 20:16371967 C 55614 NM_001199865.1 Transcript intron_variant - - - - - - rs1884599 20:16371967 C ENSESTG00000001810 ENSESTT00000004490 Transcript intron_variant - - - - - - rs1884599 20:16371967 C CCDS56178.1 CCDS56178.1 Transcript intron_variant - - - - - - rs1884599 20:16371967 C 55614 NM_024704.4 Transcript intron_variant - - - - - - rs2179481 20:16942745 T - - - intergenic_variant - - - - - - rs2143274 20:17035133 G - - - intergenic_variant - - - - - - rs6044743 20:17319091 C 5126 NM_001201528.1 Transcript intron_variant - - - - - - rs6044743 20:17319091 C 5126 NM_002594.3 Transcript intron_variant - - - - - - rs6044743 20:17319091 C ENSESTG00000034977 ENSESTT00000088431 Transcript intron_variant - - - - - - rs6044743 20:17319091 C 5126 NM_001201529.1 Transcript intron_variant - - - - - - rs6044743 20:17319091 C CCDS13125.1 CCDS13125.1 Transcript intron_variant - - - - - - rs6044743 20:17319091 C CCDS56179.1 CCDS56179.1 Transcript intron_variant - - - - - - rs6044743 20:17319091 C CCDS56180.1 CCDS56180.1 Transcript intron_variant - - - - - - rs6044743 20:17319091 C ENSESTG00000034977 ENSESTT00000088426 Transcript intron_variant - - - - - - rs201926 20:17392151 C 5126 NM_001201528.1 Transcript intron_variant - - - - - - rs201926 20:17392151 C 5126 NM_002594.3 Transcript intron_variant - - - - - - rs201926 20:17392151 C ENSESTG00000034977 ENSESTT00000088431 Transcript intron_variant - - - - - - rs201926 20:17392151 C 5126 NM_001201529.1 Transcript intron_variant - - - - - - rs201926 20:17392151 C CCDS13125.1 CCDS13125.1 Transcript intron_variant - - - - - - rs201926 20:17392151 C CCDS56179.1 CCDS56179.1 Transcript intron_variant - - - - - - rs201926 20:17392151 C CCDS56180.1 CCDS56180.1 Transcript intron_variant - - - - - - rs201926 20:17392151 C ENSESTG00000034977 ENSESTT00000088426 Transcript intron_variant - - - - - - rs2328180 20:17586469 C 11034 NM_001011546.1 Transcript intron_variant - - - - - - rs2328180 20:17586469 C ENSESTG00000034997 ENSESTT00000088464 Transcript intron_variant - - - - - - rs2328180 20:17586469 C 11034 NM_006870.3 Transcript intron_variant - - - - - - rs2328180 20:17586469 C CCDS46580.1 CCDS46580.1 Transcript intron_variant - - - - - - rs2328180 20:17586469 C ENSESTG00000034997 ENSESTT00000088465 Transcript intron_variant - - - - - - rs2328180 20:17586469 C ENSESTG00000034997 ENSESTT00000088459 Transcript intron_variant - - - - - - rs2328180 20:17586469 C CCDS13127.1 CCDS13127.1 Transcript intron_variant - - - - - - rs4814629 20:17598230 C - ENSR00000008484 RegulatoryFeature regulatory_region_variant - - - - - - rs4814629 20:17598230 C ENSESTG00000035014 ENSESTT00000088572 Transcript intron_variant - - - - - - rs4814629 20:17598230 C ENSESTG00000035014 ENSESTT00000088558 Transcript intron_variant - - - - - - rs4814629 20:17598230 C CCDS13128.1 CCDS13128.1 Transcript intron_variant - - - - - - rs4814629 20:17598230 C 6238 NM_004587.2 Transcript intron_variant - - - - - - rs4814629 20:17598230 C 6238 NM_001042576.1 Transcript intron_variant - - - - - - rs4814629 20:17598230 C ENSESTG00000035014 ENSESTT00000088574 Transcript intron_variant - - - - - - rs13040917 20:17640009 C ENSESTG00000035014 ENSESTT00000088558 Transcript upstream_gene_variant - - - - - - DISTANCE=199 rs13040917 20:17640009 C ENSESTG00000035008 ENSESTT00000088489 Transcript downstream_gene_variant - - - - - - DISTANCE=731 rs13040917 20:17640009 C ENSESTG00000035008 ENSESTT00000088485 Transcript downstream_gene_variant - - - - - - DISTANCE=643 rs13040917 20:17640009 C ENSESTG00000035014 ENSESTT00000088572 Transcript upstream_gene_variant - - - - - - DISTANCE=199 rs13040917 20:17640009 C CCDS13128.1 CCDS13128.1 Transcript intron_variant - - - - - - rs13040917 20:17640009 C 6238 NM_001042576.1 Transcript intron_variant - - - - - - rs13040917 20:17640009 C 6238 NM_004587.2 Transcript intron_variant - - - - - - rs13040917 20:17640009 C ENSESTG00000035005 ENSESTT00000088466 Transcript intron_variant - - - - - - rs2618594 20:17831063 G - ENSR00001447728 RegulatoryFeature regulatory_region_variant - - - - - - rs2618594 20:17831063 G - - - intergenic_variant - - - - - - rs2145225 20:18495522 A ENSESTG00000035181 ENSESTT00000088951 Transcript intron_variant - - - - - - rs2145225 20:18495522 A ENSESTG00000035181 ENSESTT00000088949 Transcript intron_variant - - - - - - rs2145225 20:18495522 A 10483 NM_001172745.1 Transcript intron_variant - - - - - - rs2145225 20:18495522 A 10483 NM_006363.4 Transcript intron_variant - - - - - - rs2145225 20:18495522 A 10483 NM_032986.3 Transcript intron_variant - - - - - - rs2145225 20:18495522 A ENSESTG00000035181 ENSESTT00000088944 Transcript intron_variant - - - - - - rs2145225 20:18495522 A CCDS13137.1 CCDS13137.1 Transcript intron_variant - - - - - - rs2145225 20:18495522 A 10483 NM_032985.4 Transcript intron_variant - - - - - - rs2145225 20:18495522 A 10483 NM_001172746.1 Transcript intron_variant - - - - - - rs2145225 20:18495522 A ENSESTG00000035181 ENSESTT00000088915 Transcript intron_variant - - - - - - rs4814761 20:18528343 A ENSESTG00000035181 ENSESTT00000088951 Transcript intron_variant - - - - - - rs4814761 20:18528343 A ENSESTG00000035181 ENSESTT00000088949 Transcript intron_variant - - - - - - rs4814761 20:18528343 A 10483 NM_001172745.1 Transcript intron_variant - - - - - - rs4814761 20:18528343 A 10483 NM_006363.4 Transcript intron_variant - - - - - - rs4814761 20:18528343 A 10483 NM_032986.3 Transcript intron_variant - - - - - - rs4814761 20:18528343 A ENSESTG00000035181 ENSESTT00000088944 Transcript intron_variant - - - - - - rs4814761 20:18528343 A CCDS13137.1 CCDS13137.1 Transcript intron_variant - - - - - - rs4814761 20:18528343 A 10483 NM_032985.4 Transcript intron_variant - - - - - - rs4814761 20:18528343 A 10483 NM_001172746.1 Transcript intron_variant - - - - - - rs4814761 20:18528343 A ENSESTG00000035181 ENSESTT00000088915 Transcript intron_variant - - - - - - rs6112024 20:18531499 C ENSESTG00000035181 ENSESTT00000088951 Transcript intron_variant - - - - - - rs6112024 20:18531499 C ENSESTG00000035181 ENSESTT00000088949 Transcript intron_variant - - - - - - rs6112024 20:18531499 C 10483 NM_001172745.1 Transcript intron_variant - - - - - - rs6112024 20:18531499 C ENSESTG00000035236 ENSESTT00000089010 Transcript upstream_gene_variant - - - - - - DISTANCE=4255 rs6112024 20:18531499 C 10483 NM_006363.4 Transcript intron_variant - - - - - - rs6112024 20:18531499 C 10483 NM_032986.3 Transcript intron_variant - - - - - - rs6112024 20:18531499 C ENSESTG00000035181 ENSESTT00000088944 Transcript intron_variant - - - - - - rs6112024 20:18531499 C CCDS13137.1 CCDS13137.1 Transcript intron_variant - - - - - - rs6112024 20:18531499 C 10483 NM_032985.4 Transcript intron_variant - - - - - - rs6112024 20:18531499 C 10483 NM_001172746.1 Transcript intron_variant - - - - - - rs6112024 20:18531499 C ENSESTG00000035181 ENSESTT00000088915 Transcript intron_variant - - - - - - rs56112071 20:18558496 C - - - intergenic_variant - - - - - - rs1884875 20:18576912 G CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs1884875 20:18576912 G 92675 NM_080820.4 Transcript intron_variant - - - - - - rs1884875 20:18576912 G ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs6045500 20:18589612 T CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs6045500 20:18589612 T 92675 NM_080820.4 Transcript intron_variant - - - - - - rs6045500 20:18589612 T ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs1358800 20:18594351 G - ENSR00001447770 RegulatoryFeature regulatory_region_variant - - - - - - rs1358800 20:18594351 G CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs1358800 20:18594351 G 92675 NM_080820.4 Transcript intron_variant - - - - - - rs1358800 20:18594351 G ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs1040791 20:18614847 A ENSESTG00000035245 ENSESTT00000089037 Transcript intron_variant - - - - - - rs1040791 20:18614847 A CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs1040791 20:18614847 A 92675 NM_080820.4 Transcript intron_variant - - - - - - rs1040791 20:18614847 A ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs1040791 20:18614847 A ENSESTG00000035245 ENSESTT00000089035 Transcript intron_variant - - - - - - rs2180602 20:18618896 C ENSESTG00000035245 ENSESTT00000089037 Transcript intron_variant - - - - - - rs2180602 20:18618896 C CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs2180602 20:18618896 C 92675 NM_080820.4 Transcript intron_variant - - - - - - rs2180602 20:18618896 C ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs2180602 20:18618896 C ENSESTG00000035245 ENSESTT00000089035 Transcript intron_variant - - - - - - rs6045538 20:18636174 C ENSESTG00000035245 ENSESTT00000089037 Transcript intron_variant - - - - - - rs6045538 20:18636174 C CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs6045538 20:18636174 C 92675 NM_080820.4 Transcript intron_variant - - - - - - rs6045538 20:18636174 C ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs6045538 20:18636174 C ENSESTG00000035245 ENSESTT00000089035 Transcript intron_variant - - - - - - rs4813337 20:18638646 G - ENSR00001447773 RegulatoryFeature regulatory_region_variant - - - - - - rs4813337 20:18638646 G ENSESTG00000035245 ENSESTT00000089037 Transcript intron_variant - - - - - - rs4813337 20:18638646 G CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs4813337 20:18638646 G 92675 NM_080820.4 Transcript intron_variant - - - - - - rs4813337 20:18638646 G ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs4813337 20:18638646 G ENSESTG00000035245 ENSESTT00000089035 Transcript intron_variant - - - - - - rs6075392 20:18663703 C ENSESTG00000035245 ENSESTT00000089037 Transcript intron_variant - - - - - - rs6075392 20:18663703 C CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs6075392 20:18663703 C 92675 NM_080820.4 Transcript intron_variant - - - - - - rs6075392 20:18663703 C ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs6075392 20:18663703 C ENSESTG00000035245 ENSESTT00000089035 Transcript intron_variant - - - - - - rs6081300 20:18669303 G ENSESTG00000035245 ENSESTT00000089037 Transcript intron_variant - - - - - - rs6081300 20:18669303 G CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs6081300 20:18669303 G 92675 NM_080820.4 Transcript intron_variant - - - - - - rs6081300 20:18669303 G ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs6081300 20:18669303 G ENSESTG00000035245 ENSESTT00000089035 Transcript intron_variant - - - - - - rs2208204 20:18694349 A ENSESTG00000035245 ENSESTT00000089037 Transcript intron_variant - - - - - - rs2208204 20:18694349 A CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs2208204 20:18694349 A 92675 NM_080820.4 Transcript intron_variant - - - - - - rs2208204 20:18694349 A ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs2208204 20:18694349 A ENSESTG00000035245 ENSESTT00000089035 Transcript intron_variant - - - - - - rs6035107 20:18696240 G ENSESTG00000035245 ENSESTT00000089037 Transcript intron_variant - - - - - - rs6035107 20:18696240 G CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs6035107 20:18696240 G 92675 NM_080820.4 Transcript intron_variant - - - - - - rs6035107 20:18696240 G ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs6035107 20:18696240 G ENSESTG00000035245 ENSESTT00000089035 Transcript intron_variant - - - - - - rs1321322 20:18702036 A ENSESTG00000035245 ENSESTT00000089037 Transcript intron_variant - - - - - - rs1321322 20:18702036 A CCDS13138.1 CCDS13138.1 Transcript intron_variant - - - - - - rs1321322 20:18702036 A 92675 NM_080820.4 Transcript intron_variant - - - - - - rs1321322 20:18702036 A ENSESTG00000035245 ENSESTT00000089032 Transcript intron_variant - - - - - - rs1321322 20:18702036 A ENSESTG00000035245 ENSESTT00000089035 Transcript intron_variant - - - - - - rs2206872 20:18851143 T - - - intergenic_variant - - - - - - rs6035175 20:18950719 T - - - intergenic_variant - - - - - - rs6132226 20:19652767 G ENSESTG00000022576 ENSESTT00000057021 Transcript intron_variant - - - - - - rs6132226 20:19652767 G 57419 NM_020689.3 Transcript intron_variant - - - - - - rs6132226 20:19652767 G CCDS13140.1 CCDS13140.1 Transcript intron_variant - - - - - - rs199565 20:19984708 T CCDS56182.1 CCDS56182.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3128 rs199565 20:19984708 T 54453 NM_018993.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1605 rs199565 20:19984708 T ENSESTG00000017311 ENSESTT00000043572 Transcript downstream_gene_variant - - - - - - DISTANCE=3170 rs199565 20:19984708 T ENSESTG00000017311 ENSESTT00000043556 Transcript downstream_gene_variant - - - - - - DISTANCE=3167 rs199565 20:19984708 T 54453 NM_001242581.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1605 rs975110 20:20143781 G 26074 NM_015585.3 Transcript intron_variant - - - - - - rs975110 20:20143781 G CCDS54452.1 CCDS54452.1 Transcript intron_variant - - - - - - rs975110 20:20143781 G 26074 NM_001167816.1 Transcript intron_variant - - - - - - rs975110 20:20143781 G CCDS33447.1 CCDS33447.1 Transcript intron_variant - - - - - - rs6035637 20:20478829 T - ENSR00000398823 RegulatoryFeature regulatory_region_variant - - - - - - rs6035637 20:20478829 T CCDS46584.1 CCDS46584.1 Transcript intron_variant - - - - - - rs6035637 20:20478829 T ENSESTG00000017584 ENSESTT00000044347 Transcript intron_variant - - - - - - rs6035637 20:20478829 T ENSESTG00000017584 ENSESTT00000044309 Transcript intron_variant - - - - - - rs6035637 20:20478829 T ENSESTG00000017584 ENSESTT00000044353 Transcript intron_variant - - - - - - rs6035637 20:20478829 T ENSESTG00000017584 ENSESTT00000044327 Transcript intron_variant - - - - - - rs6035637 20:20478829 T 57186 NM_020343.3 Transcript intron_variant - - - - - - rs6046913 20:20508703 C CCDS46584.1 CCDS46584.1 Transcript intron_variant - - - - - - rs6046913 20:20508703 C ENSESTG00000017490 ENSESTT00000044157 Transcript downstream_gene_variant - - - - - - DISTANCE=3694 rs6046913 20:20508703 C 57186 NM_020343.3 Transcript intron_variant - - - - - - rs6046913 20:20508703 C ENSESTG00000017574 ENSESTT00000044214 Transcript upstream_gene_variant - - - - - - DISTANCE=1725 rs6035746 20:20951924 C - - - intergenic_variant - - - - - - rs6047207 20:21004850 C - - - intergenic_variant - - - - - - rs1033685 20:21568277 T ENSESTG00000026462 ENSESTT00000066666 Transcript intron_variant - - - - - - rs2424385 20:21569793 G ENSESTG00000026462 ENSESTT00000066666 Transcript intron_variant - - - - - - rs6036031 20:22053945 G 100270679 NR_038394.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6113500 20:22064431 A - - - intergenic_variant - - - - - - rs6047875 20:22066432 G - - - intergenic_variant - - - - - - rs6048012 20:22286260 A - ENSR00001447973 RegulatoryFeature regulatory_region_variant - - - - - - rs6048012 20:22286260 A - - - intergenic_variant - - - - - - rs199795 20:22289377 G - - - intergenic_variant - - - - - - rs185639 20:22331459 T - - - intergenic_variant - - - - - - rs199772 20:22382042 T 284788 NR_027090.1 Transcript non_coding_exon_variant,nc_transcript_variant 743 - - - - - rs199772 20:22382042 T 284788 NR_027089.1 Transcript non_coding_exon_variant,nc_transcript_variant 827 - - - - - rs6048255 20:22667891 G ENSESTG00000012394 ENSESTT00000031072 Transcript upstream_gene_variant - - - - - - DISTANCE=2375 rs6048255 20:22667891 G ENSESTG00000012394 ENSESTT00000031066 Transcript upstream_gene_variant - - - - - - DISTANCE=1958 rs6048255 20:22667891 G ENSESTG00000002802 ENSESTT00000006956 Transcript intron_variant - - - - - - rs4402830 20:22882918 A - - - intergenic_variant - - - - - - rs6082918 20:22897030 A - - - intergenic_variant - - - - - - rs6048679 20:23266027 A - - - intergenic_variant - - - - - - rs2983290 20:23475818 T ENSESTG00000012313 ENSESTT00000030873 Transcript intron_variant - - - - - - rs2983290 20:23475818 T CCDS13156.1 CCDS13156.1 Transcript intron_variant - - - - - - rs2983290 20:23475818 T ENSESTG00000012341 ENSESTT00000030964 Transcript intron_variant - - - - - - rs2983290 20:23475818 T 10047 NM_005492.2 Transcript intron_variant - - - - - - rs1467500 20:23525294 T 164380 NR_001279.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2639 rs1467500 20:23525294 T ENSESTG00000012321 ENSESTT00000030893 Transcript downstream_gene_variant - - - - - - DISTANCE=2650 rs2983638 20:23583098 A 128822 NM_001008693.2 Transcript 3_prime_UTR_variant 1638 - - - - - rs2983638 20:23583098 A CCDS33450.1 CCDS33450.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1049 rs6036524 20:23753426 C ENSESTG00000021149 ENSESTT00000053100 Transcript intron_variant - - - - - - rs6036524 20:23753426 C ENSESTG00000021149 ENSESTT00000053089 Transcript intron_variant - - - - - - rs6132666 20:23781517 A ENSESTG00000021149 ENSESTT00000053100 Transcript intron_variant - - - - - - rs6132666 20:23781517 A ENSESTG00000021149 ENSESTT00000053089 Transcript intron_variant - - - - - - rs4592922 20:23850357 G - - - intergenic_variant - - - - - - rs4815268 20:24115533 T - - - intergenic_variant - - - - - - rs705645 20:24274812 A - - - intergenic_variant - - - - - - rs1331287 20:24820108 G - ENSR00000649160 RegulatoryFeature regulatory_region_variant - - - - - - rs1331287 20:24820108 G - - - intergenic_variant - - - - - - rs914307 20:24862171 G - - - intergenic_variant - - - - - - rs4815353 20:24950574 C ENSESTG00000011691 ENSESTT00000029363 Transcript intron_variant - - - - - - rs4815353 20:24950574 C 57136 NM_020531.2 Transcript intron_variant - - - - - - rs4815353 20:24950574 C CCDS13166.1 CCDS13166.1 Transcript intron_variant - - - - - - rs4815353 20:24950574 C ENSESTG00000011691 ENSESTT00000029373 Transcript intron_variant - - - - - - rs4815353 20:24950574 C ENSESTG00000011691 ENSESTT00000029325 Transcript intron_variant - - - - - - rs2482946 20:25384165 A ENSESTG00000011597 ENSESTT00000029092 Transcript upstream_gene_variant - - - - - - DISTANCE=4240 rs2482946 20:25384165 A CCDS33451.1 CCDS33451.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4292 rs2482946 20:25384165 A 9837 NM_021067.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4158 rs2482946 20:25384165 A ENSESTG00000011597 ENSESTT00000029084 Transcript upstream_gene_variant - - - - - - DISTANCE=4163 rs2482946 20:25384165 A ENSESTG00000011597 ENSESTT00000029087 Transcript upstream_gene_variant - - - - - - DISTANCE=4177 rs6050693 20:25570573 G 22981 NM_025176.4 Transcript upstream_gene_variant - - - - - - DISTANCE=4420 rs6050693 20:25570573 G ENSESTG00000011614 ENSESTT00000029119 Transcript upstream_gene_variant - - - - - - DISTANCE=4406 rs1203328 20:25885305 A - - - intergenic_variant - - - - - - rs2424801 20:29519381 G ENSESTG00000003205 ENSESTT00000007977 Transcript downstream_gene_variant - - - - - - DISTANCE=2316 rs6120332 20:29827813 A - - - intergenic_variant - - - - - - rs215911 20:30067323 G CCDS13181.1 CCDS13181.1 Transcript intron_variant - - - - - - rs215911 20:30067323 G ENSESTG00000011327 ENSESTT00000028445 Transcript intron_variant - - - - - - rs215911 20:30067323 G ENSESTG00000011327 ENSESTT00000028449 Transcript downstream_gene_variant - - - - - - DISTANCE=2667 rs215911 20:30067323 G ENSESTG00000011333 ENSESTT00000028463 Transcript upstream_gene_variant - - - - - - DISTANCE=2928 rs215911 20:30067323 G 28954 NM_014012.4 Transcript intron_variant - - - - - - rs1555285 20:30128108 G ENSESTG00000011349 ENSESTT00000028567 Transcript downstream_gene_variant - - - - - - DISTANCE=2005 rs1555285 20:30128108 G CCDS13182.1 CCDS13182.1 Transcript intron_variant - - - - - - rs1555285 20:30128108 G CCDS13183.1 CCDS13183.1 Transcript intron_variant - - - - - - rs1555285 20:30128108 G 81502 NM_178582.1 Transcript downstream_gene_variant - - - - - - DISTANCE=512 rs1555285 20:30128108 G 81502 NM_178580.1 Transcript intron_variant - - - - - - rs1555285 20:30128108 G 81502 NM_178581.1 Transcript intron_variant - - - - - - rs1555285 20:30128108 G CCDS42861.1 CCDS42861.1 Transcript intron_variant - - - - - - rs1555285 20:30128108 G 81502 NM_030789.2 Transcript intron_variant - - - - - - rs1555285 20:30128108 G ENSESTG00000011349 ENSESTT00000028564 Transcript intron_variant - - - - - - rs2209884 20:30424632 C CCDS13191.1 CCDS13191.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3032 rs2209884 20:30424632 C ENSESTG00000006872 ENSESTT00000017467 Transcript downstream_gene_variant - - - - - - DISTANCE=2587 rs2209884 20:30424632 C 85366 NM_033118.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2132 rs975651 20:30891754 C ENSESTG00000021662 ENSESTT00000054412 Transcript intron_variant - - - - - - rs975651 20:30891754 C ENSESTG00000021662 ENSESTT00000054399 Transcript intron_variant - - - - - - rs975651 20:30891754 C 9371 NM_004798.3 Transcript intron_variant - - - - - - rs6058694 20:31022959 C ENSESTG00000021764 ENSESTT00000054885 Transcript downstream_gene_variant - - - - - - DISTANCE=3669 rs6058694 20:31022959 C CCDS13201.1 CCDS13201.1 Transcript missense_variant 2444 2444 815 L/P cTg/cCg - PolyPhen=benign;SIFT=tolerated rs6058694 20:31022959 C ENSESTG00000021764 ENSESTT00000054866 Transcript downstream_gene_variant - - - - - - DISTANCE=573 rs6058694 20:31022959 C ENSESTG00000021764 ENSESTT00000054930 Transcript downstream_gene_variant - - - - - - DISTANCE=3669 rs6058694 20:31022959 C ENSESTG00000021764 ENSESTT00000054927 Transcript downstream_gene_variant - - - - - - DISTANCE=573 rs6058694 20:31022959 C 171023 NM_015338.5 Transcript missense_variant 2876 2444 815 L/P cTg/cCg - PolyPhen=benign;SIFT=tolerated rs6058694 20:31022959 C ENSESTG00000021764 ENSESTT00000054979 Transcript downstream_gene_variant - - - - - - DISTANCE=3529 rs13043294 20:31152792 C ENSESTG00000022353 ENSESTT00000056402 Transcript intron_variant - - - - - - rs13043294 20:31152792 C 140688 NM_001256798.1 Transcript intron_variant - - - - - - rs1742977 20:31163576 A ENSESTG00000022353 ENSESTT00000056402 Transcript intron_variant - - - - - - rs1742977 20:31163576 A 140688 NM_001256798.1 Transcript intron_variant - - - - - - rs461722 20:31218344 C 284805 NM_182584.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1083 rs6088131 20:31766531 G - ENSR00000399922 RegulatoryFeature regulatory_region_variant - - - - - - rs6088131 20:31766531 G 140683 NM_080574.2 Transcript intron_variant - - - - - - rs6088131 20:31766531 G ENSESTG00000012005 ENSESTT00000030109 Transcript intron_variant - - - - - - rs6088131 20:31766531 G CCDS13214.1 CCDS13214.1 Transcript intron_variant - - - - - - rs6088131 20:31766531 G ENSESTG00000012005 ENSESTT00000030087 Transcript downstream_gene_variant - - - - - - DISTANCE=4586 rs6088131 20:31766531 G ENSESTG00000012005 ENSESTT00000030096 Transcript downstream_gene_variant - - - - - - DISTANCE=3101 rs4911350 20:32195967 A CCDS46590.1 CCDS46590.1 Transcript intron_variant - - - - - - rs4911350 20:32195967 A ENSESTG00000012135 ENSESTT00000030365 Transcript intron_variant - - - - - - rs4911350 20:32195967 A 9139 NM_001039709.1 Transcript intron_variant - - - - - - rs4911350 20:32195967 A 9139 NM_001032999.2 Transcript intron_variant - - - - - - rs4911350 20:32195967 A 9139 NM_005093.3 Transcript intron_variant - - - - - - rs4911350 20:32195967 A ENSESTG00000012135 ENSESTT00000030413 Transcript intron_variant - - - - - - rs4911350 20:32195967 A ENSESTG00000012135 ENSESTT00000030414 Transcript intron_variant - - - - - - rs4911350 20:32195967 A ENSESTG00000012135 ENSESTT00000030421 Transcript intron_variant - - - - - - rs4911350 20:32195967 A ENSESTG00000012135 ENSESTT00000030429 Transcript intron_variant - - - - - - rs4911350 20:32195967 A ENSESTG00000012135 ENSESTT00000030424 Transcript downstream_gene_variant - - - - - - DISTANCE=1182 rs4911350 20:32195967 A ENSESTG00000012135 ENSESTT00000030427 Transcript intron_variant - - - - - - rs4911350 20:32195967 A CCDS13221.1 CCDS13221.1 Transcript intron_variant - - - - - - rs4911350 20:32195967 A ENSESTG00000012135 ENSESTT00000030420 Transcript intron_variant - - - - - - rs6059451 20:32338274 T CCDS13227.1 CCDS13227.1 Transcript intron_variant - - - - - - rs6059451 20:32338274 T 84905 NM_032819.3 Transcript intron_variant - - - - - - rs6059451 20:32338274 T ENSESTG00000012174 ENSESTT00000030472 Transcript intron_variant - - - - - - rs6059637 20:32616116 T ENSESTG00000014467 ENSESTT00000036330 Transcript intron_variant - - - - - - rs6059637 20:32616116 T 22913 NM_016732.2 Transcript intron_variant - - - - - - rs6059637 20:32616116 T 22913 NM_007367.3 Transcript intron_variant - - - - - - rs6059637 20:32616116 T ENSESTG00000014467 ENSESTT00000036346 Transcript upstream_gene_variant - - - - - - DISTANCE=1551 rs819170 20:32868004 G CCDS13233.1 CCDS13233.1 Transcript downstream_gene_variant - - - - - - DISTANCE=836 rs819170 20:32868004 G 191 NM_001161766.1 Transcript downstream_gene_variant - - - - - - DISTANCE=67 rs819170 20:32868004 G 191 NM_000687.2 Transcript downstream_gene_variant - - - - - - DISTANCE=67 rs819170 20:32868004 G ENSESTG00000014929 ENSESTT00000037478 Transcript intron_variant - - - - - - rs819170 20:32868004 G ENSESTG00000014929 ENSESTT00000037436 Transcript intron_variant - - - - - - rs819170 20:32868004 G CCDS54457.1 CCDS54457.1 Transcript downstream_gene_variant - - - - - - DISTANCE=836 rs1205333 20:32895923 A CCDS13233.1 CCDS13233.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4847 rs1205333 20:32895923 A 191 NM_001161766.1 Transcript intron_variant - - - - - - rs1205333 20:32895923 A ENSESTG00000014929 ENSESTT00000037443 Transcript intron_variant - - - - - - rs1205333 20:32895923 A 191 NM_000687.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4708 rs1205333 20:32895923 A ENSESTG00000014929 ENSESTT00000037478 Transcript upstream_gene_variant - - - - - - DISTANCE=4760 rs1205333 20:32895923 A ENSESTG00000014929 ENSESTT00000037436 Transcript intron_variant - - - - - - rs2425015 20:33583331 G 57644 NM_020884.3 Transcript missense_variant 3336 3019 1007 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs2425015 20:33583331 G ENSESTG00000026086 ENSESTT00000065722 Transcript 5_prime_UTR_variant 86 - - - - - rs2425015 20:33583331 G CCDS42869.1 CCDS42869.1 Transcript missense_variant 3019 3019 1007 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs2425015 20:33583331 G ENSESTG00000026091 ENSESTT00000065743 Transcript upstream_gene_variant - - - - - - DISTANCE=2857 rs2425124 20:34330259 C - ENSR00000234309 RegulatoryFeature regulatory_region_variant - - - - - - rs2425124 20:34330259 C CCDS56186.1 CCDS56186.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1463 rs2425124 20:34330259 C 9584 NM_004902.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1 rs2425124 20:34330259 C ENSESTG00000026829 ENSESTT00000067980 Transcript upstream_gene_variant - - - - - - DISTANCE=194 rs2425124 20:34330259 C ENSESTG00000026829 ENSESTT00000067960 Transcript upstream_gene_variant - - - - - - DISTANCE=184 rs2425124 20:34330259 C 9584 NM_001242599.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1 rs2425124 20:34330259 C CCDS13265.1 CCDS13265.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1463 rs2425124 20:34330259 C 9584 NR_040723.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1 rs2425124 20:34330259 C 9584 NR_040722.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1 rs2425124 20:34330259 C CCDS13266.1 CCDS13266.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1463 rs2425124 20:34330259 C 9584 NR_040724.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1 rs2425124 20:34330259 C ENSESTG00000026829 ENSESTT00000067868 Transcript upstream_gene_variant - - - - - - DISTANCE=123 rs2425124 20:34330259 C ENSESTG00000026829 ENSESTT00000067666 Transcript upstream_gene_variant - - - - - - DISTANCE=77 rs2425124 20:34330259 C ENSESTG00000026829 ENSESTT00000067894 Transcript upstream_gene_variant - - - - - - DISTANCE=123 rs2425124 20:34330259 C ENSESTG00000026829 ENSESTT00000067901 Transcript upstream_gene_variant - - - - - - DISTANCE=123 rs2425124 20:34330259 C 9584 NM_001242600.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1 rs2425124 20:34330259 C 9584 NM_184234.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1 rs2378393 20:34336778 C - - - intergenic_variant - - - - - - rs1204551 20:34630134 G - ENSR00000234336 RegulatoryFeature regulatory_region_variant - - - - - - rs1204551 20:34630134 G 647979 NR_027451.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3406 rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084276 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084359 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084306 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084300 Transcript intron_variant - - - - - - rs2746101 20:34688898 T 2036 NM_001258330.1 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084377 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084324 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084286 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084270 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084256 Transcript intron_variant - - - - - - rs2746101 20:34688898 T 2036 NM_177996.2 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084370 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084292 Transcript intron_variant - - - - - - rs2746101 20:34688898 T 2036 NM_001258329.1 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084260 Transcript intron_variant - - - - - - rs2746101 20:34688898 T 2036 NM_001258331.1 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084350 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084338 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084326 Transcript intron_variant - - - - - - rs2746101 20:34688898 T ENSESTG00000033330 ENSESTT00000084314 Transcript intron_variant - - - - - - rs1291187 20:35134711 A - ENSR00000649322 RegulatoryFeature regulatory_region_variant - - - - - - rs1291187 20:35134711 A CCDS13275.1 CCDS13275.1 Transcript intron_variant - - - - - - rs1291187 20:35134711 A CCDS13274.1 CCDS13274.1 Transcript intron_variant - - - - - - rs1291187 20:35134711 A 22839 NM_014902.4 Transcript intron_variant - - - - - - rs1291187 20:35134711 A 22839 NM_001042486.2 Transcript intron_variant - - - - - - rs1291187 20:35134711 A 22839 NM_183006.2 Transcript intron_variant - - - - - - rs578811 20:35260423 T CCDS13282.1 CCDS13282.1 Transcript intron_variant - - - - - - rs578811 20:35260423 T CCDS13283.1 CCDS13283.1 Transcript intron_variant - - - - - - rs578811 20:35260423 T ENSESTG00000033617 ENSESTT00000084998 Transcript intron_variant - - - - - - rs578811 20:35260423 T ENSESTG00000033617 ENSESTT00000085008 Transcript downstream_gene_variant - - - - - - DISTANCE=2468 rs578811 20:35260423 T ENSESTG00000033617 ENSESTT00000085003 Transcript intron_variant - - - - - - rs578811 20:35260423 T 84174 NM_175077.2 Transcript intron_variant - - - - - - rs578811 20:35260423 T 84174 NM_032214.3 Transcript intron_variant - - - - - - rs6016397 20:35379557 C 79980 NM_001145318.1 Transcript downstream_gene_variant - - - - - - DISTANCE=637 rs6016397 20:35379557 C ENSESTG00000033546 ENSESTT00000084836 Transcript downstream_gene_variant - - - - - - DISTANCE=1675 rs6016397 20:35379557 C 79980 NM_001145317.1 Transcript downstream_gene_variant - - - - - - DISTANCE=637 rs6016397 20:35379557 C CCDS46597.1 CCDS46597.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1634 rs6016397 20:35379557 C ENSESTG00000033546 ENSESTT00000084837 Transcript downstream_gene_variant - - - - - - DISTANCE=1675 rs6016397 20:35379557 C CCDS13286.1 CCDS13286.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1634 rs6016397 20:35379557 C ENSESTG00000033546 ENSESTT00000084820 Transcript downstream_gene_variant - - - - - - DISTANCE=1675 rs6016397 20:35379557 C 79980 NM_001145316.1 Transcript downstream_gene_variant - - - - - - DISTANCE=637 rs6016397 20:35379557 C 79980 NM_024918.3 Transcript downstream_gene_variant - - - - - - DISTANCE=637 rs6016397 20:35379557 C 79980 NM_001145315.1 Transcript downstream_gene_variant - - - - - - DISTANCE=637 rs6016397 20:35379557 C CCDS46596.1 CCDS46596.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1634 rs2145792 20:36031097 G ENSESTG00000028750 ENSESTT00000072451 Transcript intron_variant - - - - - - rs2145792 20:36031097 G 6714 NM_198291.1 Transcript intron_variant - - - - - - rs2145792 20:36031097 G ENSESTG00000028750 ENSESTT00000072395 Transcript downstream_gene_variant - - - - - - DISTANCE=4948 rs2145792 20:36031097 G ENSESTG00000028750 ENSESTT00000072338 Transcript downstream_gene_variant - - - - - - DISTANCE=4962 rs2145792 20:36031097 G CCDS13294.1 CCDS13294.1 Transcript intron_variant - - - - - - rs2145792 20:36031097 G 6714 NM_005417.3 Transcript intron_variant - - - - - - rs6018390 20:36043275 C - - - intergenic_variant - - - - - - rs6018391 20:36043378 C - - - intergenic_variant - - - - - - rs2425327 20:36051631 C - - - intergenic_variant - - - - - - rs6122782 20:36244379 A - ENSR00000649353 RegulatoryFeature regulatory_region_variant - - - - - - rs6122782 20:36244379 A 100861522 NR_047461.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3321 rs1556199 20:36345589 C 56259 NM_030877.3 Transcript intron_variant - - - - - - rs1556199 20:36345589 C CCDS13298.1 CCDS13298.1 Transcript intron_variant - - - - - - rs1556199 20:36345589 C ENSESTG00000028812 ENSESTT00000072909 Transcript intron_variant - - - - - - rs1556199 20:36345589 C ENSESTG00000028812 ENSESTT00000072886 Transcript intron_variant - - - - - - rs6021669 20:36520152 C - - - intergenic_variant - - - - - - rs6014317 20:36832873 A - - - intergenic_variant - - - - - - rs220493 20:37305739 T - - - intergenic_variant - - - - - - rs6071580 20:37441851 G 26051 NM_001172735.1 Transcript intron_variant - - - - - - rs6071580 20:37441851 G ENSESTG00000014132 ENSESTT00000035349 Transcript intron_variant - - - - - - rs6071580 20:37441851 G 26051 NM_015568.2 Transcript intron_variant - - - - - - rs6071580 20:37441851 G ENSESTG00000014132 ENSESTT00000035327 Transcript intron_variant - - - - - - rs6071580 20:37441851 G ENSESTG00000014238 ENSESTT00000035666 Transcript intron_variant - - - - - - rs211879 20:38424335 C - ENSR00001448811 RegulatoryFeature regulatory_region_variant - - - - - - rs211879 20:38424335 C - - - intergenic_variant - - - - - - rs6016204 20:38592060 C - - - intergenic_variant - - - - - - rs6016210 20:38609624 C - - - intergenic_variant - - - - - - rs6016238 20:38698275 T - - - intergenic_variant - - - - - - rs6028947 20:38823301 G - - - intergenic_variant - - - - - - rs911070 20:38832665 A - - - intergenic_variant - - - - - - rs761369 20:39337712 G - - - intergenic_variant - - - - - - rs2866120 20:39698552 C CCDS13312.1 CCDS13312.1 Transcript intron_variant - - - - - - rs2866120 20:39698552 C 7150 NM_003286.2 Transcript intron_variant - - - - - - rs2866120 20:39698552 C ENSESTG00000027142 ENSESTT00000068648 Transcript intron_variant - - - - - - rs3092210 20:39744810 A - ENSR00000234620 RegulatoryFeature regulatory_region_variant - - - - - - rs3092210 20:39744810 A CCDS13312.1 CCDS13312.1 Transcript intron_variant - - - - - - rs3092210 20:39744810 A 7150 NM_003286.2 Transcript intron_variant - - - - - - rs3092210 20:39744810 A ENSESTG00000027142 ENSESTT00000068648 Transcript intron_variant - - - - - - rs2866744 20:40211391 A ENSESTG00000028040 ENSESTT00000070581 Transcript intron_variant - - - - - - rs2866744 20:40211391 A ENSESTG00000028040 ENSESTT00000070576 Transcript intron_variant - - - - - - rs2866744 20:40211391 A 84181 NM_032221.3 Transcript intron_variant - - - - - - rs6030079 20:40865455 G 11122 NM_007050.5 Transcript intron_variant - - - - - - rs6030079 20:40865455 G 11122 NM_133170.3 Transcript intron_variant - - - - - - rs6030079 20:40865455 G CCDS42874.1 CCDS42874.1 Transcript intron_variant - - - - - - rs1984400 20:40910575 T 11122 NM_007050.5 Transcript intron_variant - - - - - - rs1984400 20:40910575 T 11122 NM_133170.3 Transcript intron_variant - - - - - - rs1984400 20:40910575 T CCDS42874.1 CCDS42874.1 Transcript intron_variant - - - - - - rs926993 20:41165870 T 11122 NM_007050.5 Transcript intron_variant - - - - - - rs926993 20:41165870 T 11122 NM_133170.3 Transcript intron_variant - - - - - - rs926993 20:41165870 T CCDS42874.1 CCDS42874.1 Transcript intron_variant - - - - - - rs926993 20:41165870 T ENSESTG00000018460 ENSESTT00000046439 Transcript intron_variant - - - - - - rs208239 20:41427026 A 11122 NM_007050.5 Transcript intron_variant - - - - - - rs208239 20:41427026 A 11122 NM_133170.3 Transcript intron_variant - - - - - - rs208239 20:41427026 A ENSESTG00000008105 ENSESTT00000020487 Transcript intron_variant - - - - - - rs208239 20:41427026 A ENSESTG00000008105 ENSESTT00000020484 Transcript intron_variant - - - - - - rs208239 20:41427026 A CCDS42874.1 CCDS42874.1 Transcript intron_variant - - - - - - rs208239 20:41427026 A ENSESTG00000008105 ENSESTT00000020486 Transcript intron_variant - - - - - - rs208231 20:41457209 G 11122 NM_007050.5 Transcript intron_variant - - - - - - rs208231 20:41457209 G 11122 NM_133170.3 Transcript intron_variant - - - - - - rs208231 20:41457209 G ENSESTG00000008105 ENSESTT00000020487 Transcript intron_variant - - - - - - rs208231 20:41457209 G ENSESTG00000008105 ENSESTT00000020484 Transcript intron_variant - - - - - - rs208231 20:41457209 G CCDS42874.1 CCDS42874.1 Transcript intron_variant - - - - - - rs208231 20:41457209 G ENSESTG00000008105 ENSESTT00000020486 Transcript intron_variant - - - - - - rs126630 20:41559832 T 11122 NM_007050.5 Transcript intron_variant - - - - - - rs126630 20:41559832 T 11122 NM_133170.3 Transcript intron_variant - - - - - - rs126630 20:41559832 T ENSESTG00000008105 ENSESTT00000020487 Transcript intron_variant - - - - - - rs126630 20:41559832 T ENSESTG00000008105 ENSESTT00000020484 Transcript intron_variant - - - - - - rs126630 20:41559832 T CCDS42874.1 CCDS42874.1 Transcript intron_variant - - - - - - rs126630 20:41559832 T ENSESTG00000008105 ENSESTT00000020486 Transcript intron_variant - - - - - - rs126633 20:41588700 G 11122 NM_007050.5 Transcript intron_variant - - - - - - rs126633 20:41588700 G ENSESTG00000007862 ENSESTT00000019856 Transcript intron_variant - - - - - - rs126633 20:41588700 G 11122 NM_133170.3 Transcript intron_variant - - - - - - rs126633 20:41588700 G ENSESTG00000008105 ENSESTT00000020487 Transcript intron_variant - - - - - - rs126633 20:41588700 G ENSESTG00000008105 ENSESTT00000020484 Transcript intron_variant - - - - - - rs126633 20:41588700 G CCDS42874.1 CCDS42874.1 Transcript intron_variant - - - - - - rs126633 20:41588700 G ENSESTG00000008105 ENSESTT00000020486 Transcript intron_variant - - - - - - rs206160 20:41653867 A 11122 NM_007050.5 Transcript intron_variant - - - - - - rs206160 20:41653867 A 11122 NM_133170.3 Transcript intron_variant - - - - - - rs206160 20:41653867 A CCDS42874.1 CCDS42874.1 Transcript intron_variant - - - - - - rs4812678 20:41781840 T 11122 NM_007050.5 Transcript intron_variant - - - - - - rs4812678 20:41781840 T 11122 NM_133170.3 Transcript intron_variant - - - - - - rs4812678 20:41781840 T CCDS42874.1 CCDS42874.1 Transcript intron_variant - - - - - - rs6073058 20:41981401 T - - - intergenic_variant - - - - - - rs3135418 20:42198686 C 10110 NM_016276.3 Transcript intron_variant - - - - - - rs3135418 20:42198686 C CCDS13320.1 CCDS13320.1 Transcript intron_variant - - - - - - rs3135418 20:42198686 C ENSESTG00000008083 ENSESTT00000020437 Transcript intron_variant - - - - - - rs3135418 20:42198686 C ENSESTG00000008087 ENSESTT00000020445 Transcript synonymous_variant 249 90 30 L ctC/ctG - rs3135418 20:42198686 C ENSESTG00000007957 ENSESTT00000020140 Transcript downstream_gene_variant - - - - - - DISTANCE=403 rs3135418 20:42198686 C CCDS13321.1 CCDS13321.1 Transcript intron_variant - - - - - - rs3135418 20:42198686 C 10110 NM_001199264.1 Transcript intron_variant - - - - - - rs3135418 20:42198686 C ENSESTG00000007957 ENSESTT00000020131 Transcript intron_variant - - - - - - rs3135418 20:42198686 C ENSESTG00000007957 ENSESTT00000020137 Transcript intron_variant - - - - - - rs3135418 20:42198686 C 10110 NM_170693.2 Transcript intron_variant - - - - - - rs3127058 20:42226256 G 51098 NM_016004.2 Transcript intron_variant - - - - - - rs3127058 20:42226256 G ENSESTG00000007988 ENSESTT00000020253 Transcript intron_variant - - - - - - rs3127058 20:42226256 G CCDS33470.1 CCDS33470.1 Transcript intron_variant - - - - - - rs3127058 20:42226256 G ENSESTG00000007988 ENSESTT00000020184 Transcript intron_variant - - - - - - rs3127058 20:42226256 G ENSESTG00000007988 ENSESTT00000020248 Transcript intron_variant - - - - - - rs3091982 20:42433972 T - - - intergenic_variant - - - - - - rs6103490 20:42495138 C - - - intergenic_variant - - - - - - rs1998108 20:42605653 C ENSESTG00000000673 ENSESTT00000001634 Transcript intron_variant - - - - - - rs1998108 20:42605653 C ENSESTG00000000673 ENSESTT00000001625 Transcript intron_variant - - - - - - rs1998108 20:42605653 C CCDS46603.1 CCDS46603.1 Transcript intron_variant - - - - - - rs1998108 20:42605653 C CCDS42875.1 CCDS42875.1 Transcript intron_variant - - - - - - rs1998108 20:42605653 C 84969 NM_001098796.1 Transcript intron_variant - - - - - - rs1998108 20:42605653 C ENSESTG00000000673 ENSESTT00000001620 Transcript intron_variant - - - - - - rs1998108 20:42605653 C CCDS13324.1 CCDS13324.1 Transcript intron_variant - - - - - - rs1998108 20:42605653 C 84969 NM_001098797.1 Transcript intron_variant - - - - - - rs1998108 20:42605653 C 84969 NM_032883.2 Transcript intron_variant - - - - - - rs1998108 20:42605653 C 84969 NM_001098798.1 Transcript intron_variant - - - - - - rs1018435 20:42853945 C ENSESTG00000000659 ENSESTT00000001600 Transcript 3_prime_UTR_variant 740 - - - - - rs1018435 20:42853945 C ENSESTG00000000659 ENSESTT00000001583 Transcript 3_prime_UTR_variant 571 - - - - - rs1018435 20:42853945 C 100505783 NR_038337.1 Transcript non_coding_exon_variant,nc_transcript_variant 1007 - - - - - rs1018435 20:42853945 C 100505783 NR_038339.1 Transcript non_coding_exon_variant,nc_transcript_variant 719 - - - - - rs1018435 20:42853945 C 100505783 NR_038338.1 Transcript non_coding_exon_variant,nc_transcript_variant 876 - - - - - rs6073401 20:42939750 C - ENSR00000119718 RegulatoryFeature regulatory_region_variant - - - - - - rs6073401 20:42939750 C ENSESTG00000000704 ENSESTT00000001686 Transcript downstream_gene_variant - - - - - - DISTANCE=4120 rs6073401 20:42939750 C CCDS33473.1 CCDS33473.1 Transcript synonymous_variant 39 39 13 G ggA/ggG - rs6073401 20:42939750 C ENSESTG00000000704 ENSESTT00000001689 Transcript downstream_gene_variant - - - - - - DISTANCE=4884 rs6073401 20:42939750 C ENSESTG00000000704 ENSESTT00000001681 Transcript downstream_gene_variant - - - - - - DISTANCE=3974 rs6073401 20:42939750 C 128486 NM_001080472.1 Transcript synonymous_variant 140 39 13 G ggA/ggG - rs244074 20:43254490 G ENSESTG00000000753 ENSESTT00000001860 Transcript intron_variant - - - - - - rs244074 20:43254490 G ENSESTG00000000753 ENSESTT00000001854 Transcript intron_variant - - - - - - rs244074 20:43254490 G CCDS13335.1 CCDS13335.1 Transcript intron_variant - - - - - - rs244074 20:43254490 G ENSESTG00000000753 ENSESTT00000001852 Transcript intron_variant - - - - - - rs244074 20:43254490 G ENSESTG00000000753 ENSESTT00000001812 Transcript downstream_gene_variant - - - - - - DISTANCE=668 rs244074 20:43254490 G ENSESTG00000000753 ENSESTT00000001859 Transcript intron_variant - - - - - - rs244074 20:43254490 G 100 NM_000022.2 Transcript intron_variant - - - - - - rs244074 20:43254490 G ENSESTG00000000753 ENSESTT00000001863 Transcript intron_variant - - - - - - rs966997 20:43320336 G - ENSR00001449065 RegulatoryFeature regulatory_region_variant - - - - - - rs966997 20:43320336 G - - - intergenic_variant - - - - - - rs1884672 20:43375256 T CCDS13337.1 CCDS13337.1 Transcript intron_variant - - - - - - rs1884672 20:43375256 T ENSESTG00000007945 ENSESTT00000020058 Transcript intron_variant - - - - - - rs1884672 20:43375256 T ENSESTG00000007945 ENSESTT00000020066 Transcript intron_variant - - - - - - rs1884672 20:43375256 T 60598 NM_022358.3 Transcript intron_variant - - - - - - rs1005284 20:43977278 C - ENSR00000119778 RegulatoryFeature regulatory_region_variant - - - - - - rs1005284 20:43977278 C CCDS13350.1 CCDS13350.1 Transcript upstream_gene_variant - - - - - - DISTANCE=254 rs1005284 20:43977278 C 6385 NM_002999.3 Transcript upstream_gene_variant - - - - - - DISTANCE=214 rs1005284 20:43977278 C ENSESTG00000008779 ENSESTT00000022082 Transcript upstream_gene_variant - - - - - - DISTANCE=214 rs1005284 20:43977278 C ENSESTG00000008779 ENSESTT00000022078 Transcript upstream_gene_variant - - - - - - DISTANCE=214 rs197668 20:44471016 C - ENSR00000401680 RegulatoryFeature regulatory_region_variant - - - - - - rs197668 20:44471016 C 10005 NM_005469.3 Transcript intron_variant - - - - - - rs197668 20:44471016 C 90203 NM_001042633.1 Transcript 3_prime_UTR_variant 2286 - - - - - rs197668 20:44471016 C CCDS13376.1 CCDS13376.1 Transcript downstream_gene_variant - - - - - - DISTANCE=334 rs197668 20:44471016 C CCDS42883.1 CCDS42883.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1720 rs197668 20:44471016 C ENSESTG00000023527 ENSESTT00000059385 Transcript intron_variant - - - - - - rs197668 20:44471016 C 90203 NM_001042632.1 Transcript 3_prime_UTR_variant 2268 - - - - - rs197668 20:44471016 C 90203 NM_033421.2 Transcript 3_prime_UTR_variant 2275 - - - - - rs197668 20:44471016 C ENSESTG00000023527 ENSESTT00000059498 Transcript intron_variant - - - - - - rs197668 20:44471016 C CCDS13377.1 CCDS13377.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1064 rs197668 20:44471016 C CCDS13378.1 CCDS13378.1 Transcript intron_variant - - - - - - rs197668 20:44471016 C ENSESTG00000020664 ENSESTT00000051835 Transcript downstream_gene_variant - - - - - - DISTANCE=1592 rs197668 20:44471016 C ENSESTG00000023527 ENSESTT00000059390 Transcript intron_variant - - - - - - rs197668 20:44471016 C ENSESTG00000020664 ENSESTT00000051850 Transcript downstream_gene_variant - - - - - - DISTANCE=1540 rs197668 20:44471016 C ENSESTG00000023527 ENSESTT00000059500 Transcript downstream_gene_variant - - - - - - DISTANCE=1276 rs197668 20:44471016 C ENSESTG00000023527 ENSESTT00000059448 Transcript intron_variant - - - - - - rs197668 20:44471016 C 90203 NM_152897.1 Transcript 3_prime_UTR_variant 1023 - - - - - rs197668 20:44471016 C ENSESTG00000023527 ENSESTT00000059405 Transcript downstream_gene_variant - - - - - - DISTANCE=1276 rs197668 20:44471016 C ENSESTG00000023527 ENSESTT00000059488 Transcript downstream_gene_variant - - - - - - DISTANCE=1276 rs578122 20:44540499 C - ENSR00000119798 RegulatoryFeature regulatory_region_variant - - - - - - rs578122 20:44540499 C CCDS13387.1 CCDS13387.1 Transcript upstream_gene_variant - - - - - - DISTANCE=408 rs578122 20:44540499 C CCDS13386.1 CCDS13386.1 Transcript upstream_gene_variant - - - - - - DISTANCE=408 rs578122 20:44540499 C ENSESTG00000023415 ENSESTT00000059028 Transcript upstream_gene_variant - - - - - - DISTANCE=627 rs578122 20:44540499 C 5360 NM_001242920.1 Transcript intron_variant - - - - - - rs578122 20:44540499 C 5360 NM_006227.3 Transcript intron_variant - - - - - - rs578122 20:44540499 C 5360 NM_182676.2 Transcript intron_variant - - - - - - rs578122 20:44540499 C ENSESTG00000023415 ENSESTT00000059251 Transcript upstream_gene_variant - - - - - - DISTANCE=866 rs578122 20:44540499 C CCDS56196.1 CCDS56196.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1854 rs578122 20:44540499 C CCDS56197.1 CCDS56197.1 Transcript upstream_gene_variant - - - - - - DISTANCE=408 rs578122 20:44540499 C 5360 NM_001242921.1 Transcript upstream_gene_variant - - - - - - DISTANCE=866 rs1467552 20:44962372 C - - - intergenic_variant - - - - - - rs375849 20:45229774 G 64849 NM_022829.5 Transcript intron_variant - - - - - - rs375849 20:45229774 G 64849 NM_001193342.1 Transcript intron_variant - - - - - - rs375849 20:45229774 G ENSESTG00000022245 ENSESTT00000056067 Transcript intron_variant - - - - - - rs375849 20:45229774 G CCDS54469.1 CCDS54469.1 Transcript intron_variant - - - - - - rs375849 20:45229774 G 64849 NM_001011554.2 Transcript intron_variant - - - - - - rs375849 20:45229774 G CCDS13400.1 CCDS13400.1 Transcript intron_variant - - - - - - rs375849 20:45229774 G ENSESTG00000022245 ENSESTT00000056156 Transcript upstream_gene_variant - - - - - - DISTANCE=1856 rs375849 20:45229774 G CCDS54470.1 CCDS54470.1 Transcript intron_variant - - - - - - rs375849 20:45229774 G 64849 NM_001193340.1 Transcript intron_variant - - - - - - rs375849 20:45229774 G CCDS42886.1 CCDS42886.1 Transcript intron_variant - - - - - - rs375849 20:45229774 G 64849 NM_001193339.1 Transcript intron_variant - - - - - - rs375849 20:45229774 G ENSESTG00000022245 ENSESTT00000056151 Transcript upstream_gene_variant - - - - - - DISTANCE=519 rs417546 20:45229777 G 64849 NM_022829.5 Transcript intron_variant - - - - - - rs417546 20:45229777 G 64849 NM_001193342.1 Transcript intron_variant - - - - - - rs417546 20:45229777 G ENSESTG00000022245 ENSESTT00000056067 Transcript intron_variant - - - - - - rs417546 20:45229777 G CCDS54469.1 CCDS54469.1 Transcript intron_variant - - - - - - rs417546 20:45229777 G 64849 NM_001011554.2 Transcript intron_variant - - - - - - rs417546 20:45229777 G CCDS13400.1 CCDS13400.1 Transcript intron_variant - - - - - - rs417546 20:45229777 G ENSESTG00000022245 ENSESTT00000056156 Transcript upstream_gene_variant - - - - - - DISTANCE=1859 rs417546 20:45229777 G CCDS54470.1 CCDS54470.1 Transcript intron_variant - - - - - - rs417546 20:45229777 G 64849 NM_001193340.1 Transcript intron_variant - - - - - - rs417546 20:45229777 G CCDS42886.1 CCDS42886.1 Transcript intron_variant - - - - - - rs417546 20:45229777 G 64849 NM_001193339.1 Transcript intron_variant - - - - - - rs417546 20:45229777 G ENSESTG00000022245 ENSESTT00000056151 Transcript upstream_gene_variant - - - - - - DISTANCE=522 rs1206802 20:45640515 G CCDS13403.1 CCDS13403.1 Transcript intron_variant - - - - - - rs1206802 20:45640515 G 2139 NM_172110.3 Transcript intron_variant - - - - - - rs1206802 20:45640515 G ENSESTG00000006148 ENSESTT00000015522 Transcript intron_variant - - - - - - rs1206802 20:45640515 G ENSESTG00000006148 ENSESTT00000015525 Transcript intron_variant - - - - - - rs1206802 20:45640515 G ENSESTG00000006148 ENSESTT00000015531 Transcript upstream_gene_variant - - - - - - DISTANCE=4294 rs1206802 20:45640515 G 2139 NM_005244.4 Transcript intron_variant - - - - - - rs1206802 20:45640515 G ENSESTG00000006148 ENSESTT00000015528 Transcript intron_variant - - - - - - rs1206802 20:45640515 G CCDS54471.1 CCDS54471.1 Transcript intron_variant - - - - - - rs1206802 20:45640515 G ENSESTG00000006148 ENSESTT00000015519 Transcript intron_variant - - - - - - rs1206802 20:45640515 G ENSESTG00000006148 ENSESTT00000015524 Transcript intron_variant - - - - - - rs1206803 20:45643762 T CCDS13403.1 CCDS13403.1 Transcript intron_variant - - - - - - rs1206803 20:45643762 T 2139 NM_172110.3 Transcript intron_variant - - - - - - rs1206803 20:45643762 T ENSESTG00000006148 ENSESTT00000015522 Transcript intron_variant - - - - - - rs1206803 20:45643762 T ENSESTG00000006173 ENSESTT00000015536 Transcript upstream_gene_variant - - - - - - DISTANCE=2789 rs1206803 20:45643762 T ENSESTG00000006148 ENSESTT00000015525 Transcript intron_variant - - - - - - rs1206803 20:45643762 T ENSESTG00000006148 ENSESTT00000015531 Transcript upstream_gene_variant - - - - - - DISTANCE=1047 rs1206803 20:45643762 T 2139 NM_005244.4 Transcript intron_variant - - - - - - rs1206803 20:45643762 T ENSESTG00000006148 ENSESTT00000015528 Transcript intron_variant - - - - - - rs1206803 20:45643762 T CCDS54471.1 CCDS54471.1 Transcript intron_variant - - - - - - rs1206803 20:45643762 T ENSESTG00000006148 ENSESTT00000015519 Transcript intron_variant - - - - - - rs1206803 20:45643762 T ENSESTG00000006148 ENSESTT00000015524 Transcript intron_variant - - - - - - rs2057086 20:45820578 A CCDS13403.1 CCDS13403.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3797 rs2057086 20:45820578 A ENSESTG00000006148 ENSESTT00000015531 Transcript downstream_gene_variant - - - - - - DISTANCE=3086 rs2057086 20:45820578 A 2139 NM_005244.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3086 rs2057086 20:45820578 A 2139 NM_172110.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3086 rs2057086 20:45820578 A CCDS54471.1 CCDS54471.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3797 rs2057086 20:45820578 A ENSESTG00000006148 ENSESTT00000015524 Transcript downstream_gene_variant - - - - - - DISTANCE=3086 rs2057086 20:45820578 A ENSESTG00000006148 ENSESTT00000015519 Transcript downstream_gene_variant - - - - - - DISTANCE=3086 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000016007 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015970 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015926 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015910 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G CCDS13405.1 CCDS13405.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3389 rs3091978 20:45836017 G 23613 NM_183047.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2364 rs3091978 20:45836017 G 23613 NM_012408.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2364 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015957 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000016031 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015939 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015967 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015913 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000016022 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015995 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015952 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000016030 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000016006 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G 23613 NM_183048.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2364 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015997 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G CCDS46613.1 CCDS46613.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3389 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015980 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000016023 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015983 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000016042 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015935 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs3091978 20:45836017 G CCDS13404.1 CCDS13404.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3389 rs3091978 20:45836017 G ENSESTG00000006289 ENSESTT00000015925 Transcript downstream_gene_variant - - - - - - DISTANCE=3503 rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015921 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016034 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016007 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015970 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015958 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015942 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015910 Transcript intron_variant - - - - - - rs6018407 20:45941411 A CCDS13405.1 CCDS13405.1 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015930 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015957 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016036 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016031 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015988 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015939 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016014 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016002 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015913 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016008 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015995 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015952 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016030 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016006 Transcript intron_variant - - - - - - rs6018407 20:45941411 A 23613 NM_183048.1 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015997 Transcript intron_variant - - - - - - rs6018407 20:45941411 A CCDS46613.1 CCDS46613.1 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015946 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016023 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015983 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015935 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006175 ENSESTT00000015546 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015925 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016000 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015926 Transcript intron_variant - - - - - - rs6018407 20:45941411 A 23613 NM_183047.1 Transcript intron_variant - - - - - - rs6018407 20:45941411 A 23613 NM_012408.3 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015928 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016039 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015967 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016022 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015918 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016029 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015962 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015973 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016025 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015923 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015980 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015976 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000016012 Transcript intron_variant - - - - - - rs6018407 20:45941411 A CCDS13404.1 CCDS13404.1 Transcript intron_variant - - - - - - rs6018407 20:45941411 A ENSESTG00000006289 ENSESTT00000015987 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015921 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016034 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016007 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015970 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015958 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015942 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015910 Transcript intron_variant - - - - - - rs3091697 20:45974963 C CCDS13405.1 CCDS13405.1 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015930 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015957 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016036 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016031 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015988 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015939 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016014 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016002 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015913 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016008 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015995 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015952 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016030 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016006 Transcript intron_variant - - - - - - rs3091697 20:45974963 C 23613 NM_183048.1 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015997 Transcript intron_variant - - - - - - rs3091697 20:45974963 C CCDS46613.1 CCDS46613.1 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015946 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016023 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015983 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015935 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006175 ENSESTT00000015546 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015925 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016000 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015926 Transcript intron_variant - - - - - - rs3091697 20:45974963 C 23613 NM_183047.1 Transcript intron_variant - - - - - - rs3091697 20:45974963 C 23613 NM_012408.3 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015928 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016039 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015967 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016022 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015918 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016029 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015962 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015973 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016025 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015923 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015980 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015976 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000016012 Transcript intron_variant - - - - - - rs3091697 20:45974963 C CCDS13404.1 CCDS13404.1 Transcript intron_variant - - - - - - rs3091697 20:45974963 C ENSESTG00000006289 ENSESTT00000015987 Transcript intron_variant - - - - - - rs1741524 20:46413497 C - ENSR00001449320 RegulatoryFeature regulatory_region_variant - - - - - - rs1741524 20:46413497 C 55959 NM_018837.3 Transcript intron_variant - - - - - - rs1741524 20:46413497 C 55959 NM_001161841.1 Transcript intron_variant - - - - - - rs1741524 20:46413497 C 55959 NM_198596.2 Transcript intron_variant - - - - - - rs1741524 20:46413497 C ENSESTG00000034835 ENSESTT00000088049 Transcript intron_variant - - - - - - rs1741524 20:46413497 C ENSESTG00000034835 ENSESTT00000088062 Transcript intron_variant - - - - - - rs2426056 20:46567782 G - - - intergenic_variant - - - - - - rs228208 20:46799638 A - - - intergenic_variant - - - - - - rs394362 20:46865685 A - - - intergenic_variant - - - - - - rs437315 20:46972678 C ENSESTG00000034830 ENSESTT00000088041 Transcript upstream_gene_variant - - - - - - DISTANCE=1000 rs4239656 20:47249921 T 57580 NM_020820.3 Transcript intron_variant - - - - - - rs4239656 20:47249921 T ENSESTG00000034809 ENSESTT00000088034 Transcript intron_variant - - - - - - rs4239656 20:47249921 T CCDS13410.1 CCDS13410.1 Transcript intron_variant - - - - - - rs1115534 20:47590426 A 10564 NM_006420.2 Transcript intron_variant - - - - - - rs1115534 20:47590426 A ENSESTG00000019709 ENSESTT00000049411 Transcript intron_variant - - - - - - rs1115534 20:47590426 A ENSESTG00000019662 ENSESTT00000049377 Transcript downstream_gene_variant - - - - - - DISTANCE=2634 rs1115534 20:47590426 A CCDS13411.1 CCDS13411.1 Transcript intron_variant - - - - - - rs554822 20:48097770 T CCDS13418.1 CCDS13418.1 Transcript intron_variant - - - - - - rs554822 20:48097770 T 3745 NM_004975.2 Transcript intron_variant - - - - - - rs554822 20:48097770 T ENSESTG00000020387 ENSESTT00000051121 Transcript intron_variant - - - - - - rs575253 20:48137890 G ENSESTG00000020338 ENSESTT00000051090 Transcript intron_variant - - - - - - rs575253 20:48137890 G CCDS13419.1 CCDS13419.1 Transcript intron_variant - - - - - - rs575253 20:48137890 G ENSESTG00000020338 ENSESTT00000051061 Transcript intron_variant - - - - - - rs575253 20:48137890 G 5740 NM_000961.3 Transcript intron_variant - - - - - - rs575253 20:48137890 G ENSESTG00000020338 ENSESTT00000051011 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NR_047554.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6012831 20:48713049 A 7335 NM_001257395.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NR_047555.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6012831 20:48713049 A 7335 NM_001257399.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A CCDS33483.1 CCDS33483.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A CCDS13426.1 CCDS13426.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NM_022442.5 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NM_001257394.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NR_047556.1 Transcript non_coding_exon_variant,nc_transcript_variant 264 - - - - - rs6012831 20:48713049 A ENSESTG00000005444 ENSESTT00000013873 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NM_001257393.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A CCDS13427.1 CCDS13427.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NM_001032288.2 Transcript intron_variant - - - - - - rs6012831 20:48713049 A ENSESTG00000005444 ENSESTT00000013876 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 387522 NM_199203.2 Transcript intron_variant - - - - - - rs6012831 20:48713049 A CCDS58775.1 CCDS58775.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A ENSESTG00000005444 ENSESTT00000013847 Transcript intron_variant - - - - - - rs6012831 20:48713049 A CCDS13424.1 CCDS13424.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NM_001257398.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NM_021988.5 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NM_001257397.1 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NR_047553.1 Transcript non_coding_exon_variant,nc_transcript_variant 647 - - - - - rs6012831 20:48713049 A 7335 NM_199144.2 Transcript intron_variant - - - - - - rs6012831 20:48713049 A 7335 NM_001257396.1 Transcript intron_variant - - - - - - rs1570180 20:49171428 A - ENSR00000649763 RegulatoryFeature regulatory_region_variant - - - - - - rs1570180 20:49171428 A ENSESTG00000005411 ENSESTT00000013787 Transcript intron_variant - - - - - - rs1570180 20:49171428 A 5770 NM_002827.2 Transcript intron_variant - - - - - - rs1570180 20:49171428 A ENSESTG00000005411 ENSESTT00000013773 Transcript intron_variant - - - - - - rs1570180 20:49171428 A CCDS13430.1 CCDS13430.1 Transcript intron_variant - - - - - - rs1570180 20:49171428 A ENSESTG00000005411 ENSESTT00000013782 Transcript intron_variant - - - - - - rs1570180 20:49171428 A ENSESTG00000005440 ENSESTT00000013823 Transcript intron_variant - - - - - - rs2870018 20:49473868 A CCDS33487.1 CCDS33487.1 Transcript intron_variant - - - - - - rs2870018 20:49473868 A 55653 NM_017843.3 Transcript intron_variant - - - - - - rs2870018 20:49473868 A 55653 NM_198799.2 Transcript intron_variant - - - - - - rs2870018 20:49473868 A CCDS13432.2 CCDS13432.2 Transcript intron_variant - - - - - - rs2870018 20:49473868 A ENSESTG00000013669 ENSESTT00000034210 Transcript intron_variant - - - - - - rs2870018 20:49473868 A 55653 NM_001010974.1 Transcript intron_variant - - - - - - rs2870018 20:49473868 A ENSESTG00000013669 ENSESTT00000034201 Transcript intron_variant - - - - - - rs2904288 20:49494842 G CCDS33487.1 CCDS33487.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1770 rs2904288 20:49494842 G 55653 NM_017843.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1128 rs2904288 20:49494842 G 55653 NM_198799.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1128 rs2904288 20:49494842 G CCDS13432.2 CCDS13432.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1697 rs2904288 20:49494842 G ENSESTG00000013669 ENSESTT00000034210 Transcript downstream_gene_variant - - - - - - DISTANCE=1129 rs2904288 20:49494842 G 55653 NM_001010974.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1128 rs2904288 20:49494842 G ENSESTG00000013669 ENSESTT00000034201 Transcript downstream_gene_variant - - - - - - DISTANCE=1129 rs6020826 20:49503801 C 23394 NM_015339.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3082 rs6020826 20:49503801 C 23394 NM_181442.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3082 rs6020826 20:49503801 C ENSESTG00000013690 ENSESTT00000034219 Transcript downstream_gene_variant - - - - - - DISTANCE=3172 rs6020826 20:49503801 C CCDS13433.1 CCDS13433.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4141 rs6020917 20:49639367 C - ENSR00000402789 RegulatoryFeature regulatory_region_variant - - - - - - rs6020917 20:49639367 C ENSESTG00000013740 ENSESTT00000034293 Transcript intron_variant - - - - - - rs6020917 20:49639367 C 3755 NM_002237.3 Transcript intron_variant - - - - - - rs4811113 20:49646201 T - - - intergenic_variant - - - - - - rs2426234 20:49648579 C - - - intergenic_variant - - - - - - rs6013194 20:50100204 A CCDS46614.1 CCDS46614.1 Transcript intron_variant - - - - - - rs6013194 20:50100204 A 4773 NM_001136021.2 Transcript intron_variant - - - - - - rs6013194 20:50100204 A 4773 NM_001258292.1 Transcript intron_variant - - - - - - rs6013194 20:50100204 A 4773 NM_001258295.1 Transcript intron_variant - - - - - - rs6013194 20:50100204 A 4773 NM_173091.3 Transcript intron_variant - - - - - - rs6013194 20:50100204 A 4773 NM_001258297.1 Transcript intron_variant - - - - - - rs6013194 20:50100204 A ENSESTG00000013721 ENSESTT00000034273 Transcript intron_variant - - - - - - rs6013194 20:50100204 A CCDS33488.1 CCDS33488.1 Transcript intron_variant - - - - - - rs6013194 20:50100204 A CCDS13437.1 CCDS13437.1 Transcript intron_variant - - - - - - rs6013194 20:50100204 A 4773 NM_001258296.1 Transcript intron_variant - - - - - - rs6013194 20:50100204 A 4773 NM_001258294.1 Transcript intron_variant - - - - - - rs6013194 20:50100204 A 4773 NM_012340.4 Transcript intron_variant - - - - - - rs6021256 20:50119347 A CCDS46614.1 CCDS46614.1 Transcript intron_variant - - - - - - rs6021256 20:50119347 A 4773 NM_001136021.2 Transcript intron_variant - - - - - - rs6021256 20:50119347 A 4773 NM_001258292.1 Transcript intron_variant - - - - - - rs6021256 20:50119347 A 4773 NM_001258295.1 Transcript intron_variant - - - - - - rs6021256 20:50119347 A 4773 NM_173091.3 Transcript intron_variant - - - - - - rs6021256 20:50119347 A 4773 NM_001258297.1 Transcript intron_variant - - - - - - rs6021256 20:50119347 A ENSESTG00000013721 ENSESTT00000034273 Transcript intron_variant - - - - - - rs6021256 20:50119347 A CCDS33488.1 CCDS33488.1 Transcript intron_variant - - - - - - rs6021256 20:50119347 A CCDS13437.1 CCDS13437.1 Transcript intron_variant - - - - - - rs6021256 20:50119347 A 4773 NM_001258296.1 Transcript intron_variant - - - - - - rs6021256 20:50119347 A 4773 NM_001258294.1 Transcript intron_variant - - - - - - rs6021256 20:50119347 A 4773 NM_012340.4 Transcript intron_variant - - - - - - rs6013207 20:50129832 C CCDS46614.1 CCDS46614.1 Transcript intron_variant - - - - - - rs6013207 20:50129832 C 4773 NM_001136021.2 Transcript intron_variant - - - - - - rs6013207 20:50129832 C 4773 NM_001258292.1 Transcript intron_variant - - - - - - rs6013207 20:50129832 C 4773 NM_001258295.1 Transcript intron_variant - - - - - - rs6013207 20:50129832 C 4773 NM_173091.3 Transcript intron_variant - - - - - - rs6013207 20:50129832 C 4773 NM_001258297.1 Transcript intron_variant - - - - - - rs6013207 20:50129832 C ENSESTG00000013721 ENSESTT00000034273 Transcript intron_variant - - - - - - rs6013207 20:50129832 C CCDS33488.1 CCDS33488.1 Transcript intron_variant - - - - - - rs6013207 20:50129832 C CCDS13437.1 CCDS13437.1 Transcript intron_variant - - - - - - rs6013207 20:50129832 C 4773 NM_001258296.1 Transcript intron_variant - - - - - - rs6013207 20:50129832 C 4773 NM_001258294.1 Transcript intron_variant - - - - - - rs6013207 20:50129832 C 4773 NM_012340.4 Transcript intron_variant - - - - - - rs1033663 20:51025621 G ENSESTG00000004483 ENSESTT00000011316 Transcript intron_variant - - - - - - rs2179460 20:51336124 C - - - intergenic_variant - - - - - - rs241801 20:51362095 G - - - intergenic_variant - - - - - - rs2747394 20:51666821 C CCDS33490.1 CCDS33490.1 Transcript intron_variant - - - - - - rs2747394 20:51666821 C 128553 NM_173485.5 Transcript intron_variant - - - - - - rs6512875 20:51850061 A CCDS33490.1 CCDS33490.1 Transcript intron_variant - - - - - - rs6512875 20:51850061 A ENSESTG00000030139 ENSESTT00000075851 Transcript intron_variant - - - - - - rs6512875 20:51850061 A 128553 NM_001193421.1 Transcript intron_variant - - - - - - rs6512875 20:51850061 A 128553 NM_173485.5 Transcript intron_variant - - - - - - rs6512875 20:51850061 A CCDS54474.1 CCDS54474.1 Transcript intron_variant - - - - - - rs6022627 20:52260107 G - ENSR00001449815 RegulatoryFeature regulatory_region_variant - - - - - - rs6022627 20:52260107 G - - - intergenic_variant - - - - - - rs6022684 20:52326118 C - - - intergenic_variant - - - - - - rs6063980 20:52330122 A - - - intergenic_variant - - - - - - rs524921 20:52683272 C - ENSR00000403219 RegulatoryFeature regulatory_region_variant - - - - - - rs524921 20:52683272 C 100616225 NR_039913.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1675 rs524921 20:52683272 C ENSESTG00000031627 ENSESTT00000079870 Transcript intron_variant - - - - - - rs524921 20:52683272 C 8537 NM_003657.2 Transcript intron_variant - - - - - - rs524921 20:52683272 C ENSESTG00000031627 ENSESTT00000079885 Transcript intron_variant - - - - - - rs1150412 20:52954222 G - - - intergenic_variant - - - - - - rs1150416 20:52956235 G - - - intergenic_variant - - - - - - rs1229990 20:53152568 T ENSESTG00000031603 ENSESTT00000079735 Transcript intron_variant - - - - - - rs1229990 20:53152568 T CCDS13446.1 CCDS13446.1 Transcript intron_variant - - - - - - rs1229990 20:53152568 T 55816 NM_018431.3 Transcript intron_variant - - - - - - rs1229990 20:53152568 T ENSESTG00000031603 ENSESTT00000079711 Transcript intron_variant - - - - - - rs157632 20:53470878 C - - - intergenic_variant - - - - - - rs6023954 20:53830319 T ENSESTG00000014997 ENSESTT00000037582 Transcript intron_variant - - - - - - rs6069416 20:54409062 A - - - intergenic_variant - - - - - - rs4811649 20:54602039 C - - - intergenic_variant - - - - - - rs6014595 20:54654077 T - - - intergenic_variant - - - - - - rs2148214 20:54847481 G - - - intergenic_variant - - - - - - rs2426625 20:54996094 G ENSESTG00000031580 ENSESTT00000079666 Transcript intron_variant - - - - - - rs2426625 20:54996094 G 57091 NM_020356.3 Transcript intron_variant - - - - - - rs2426625 20:54996094 G 57091 NM_001164115.1 Transcript intron_variant - - - - - - rs2426625 20:54996094 G CCDS54475.1 CCDS54475.1 Transcript intron_variant - - - - - - rs2426625 20:54996094 G ENSESTG00000031580 ENSESTT00000079717 Transcript upstream_gene_variant - - - - - - DISTANCE=2039 rs2426625 20:54996094 G ENSESTG00000031580 ENSESTT00000079686 Transcript intron_variant - - - - - - rs2426625 20:54996094 G 57091 NM_001164116.1 Transcript intron_variant - - - - - - rs2426625 20:54996094 G CCDS33492.1 CCDS33492.1 Transcript intron_variant - - - - - - rs2426625 20:54996094 G ENSESTG00000031580 ENSESTT00000079629 Transcript intron_variant - - - - - - rs2426625 20:54996094 G ENSESTG00000031580 ENSESTT00000079706 Transcript intron_variant - - - - - - rs2426625 20:54996094 G 57091 NM_001164114.1 Transcript intron_variant - - - - - - rs4810043 20:55391003 C - - - intergenic_variant - - - - - - rs932884 20:55411539 T - - - intergenic_variant - - - - - - rs2426719 20:55991621 G - - - intergenic_variant - - - - - - rs1475476 20:56050127 C - ENSR00000403543 RegulatoryFeature regulatory_region_variant - - - - - - rs1475476 20:56050127 C - - - intergenic_variant - - - - - - rs2865385 20:56065693 A - - - intergenic_variant - - - - - - rs6025833 20:56429493 T - - - intergenic_variant - - - - - - rs4811942 20:56476430 G - - - intergenic_variant - - - - - - rs502734 20:56761557 C - - - intergenic_variant - - - - - - rs2024553 20:56971603 T CCDS56198.1 CCDS56198.1 Transcript intron_variant - - - - - - rs2024553 20:56971603 T ENSESTG00000016205 ENSESTT00000040775 Transcript intron_variant - - - - - - rs2024553 20:56971603 T 9217 NR_036633.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2024553 20:56971603 T 9217 NM_001195677.1 Transcript intron_variant - - - - - - rs2024553 20:56971603 T CCDS33498.1 CCDS33498.1 Transcript intron_variant - - - - - - rs2024553 20:56971603 T ENSESTG00000016205 ENSESTT00000040767 Transcript intron_variant - - - - - - rs2024553 20:56971603 T 9217 NM_004738.4 Transcript intron_variant - - - - - - rs4812006 20:57059574 C ENSESTG00000016276 ENSESTT00000040865 Transcript intron_variant - - - - - - rs4812006 20:57059574 C CCDS13467.1 CCDS13467.1 Transcript intron_variant - - - - - - rs4812006 20:57059574 C 164284 NM_153360.1 Transcript intron_variant - - - - - - rs4810142 20:57245425 A 8675 NR_037943.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4810142 20:57245425 A 8675 NM_001134773.2 Transcript intron_variant - - - - - - rs4810142 20:57245425 A ENSESTG00000026819 ENSESTT00000067737 Transcript intron_variant - - - - - - rs4810142 20:57245425 A CCDS56199.1 CCDS56199.1 Transcript intron_variant - - - - - - rs4810142 20:57245425 A CCDS13468.1 CCDS13468.1 Transcript intron_variant - - - - - - rs4810142 20:57245425 A CCDS46620.1 CCDS46620.1 Transcript intron_variant - - - - - - rs4810142 20:57245425 A 8675 NM_001001433.2 Transcript intron_variant - - - - - - rs4810142 20:57245425 A ENSESTG00000027564 ENSESTT00000069378 Transcript upstream_gene_variant - - - - - - DISTANCE=2840 rs4810142 20:57245425 A 100534593 NR_037945.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4810142 20:57245425 A CCDS46619.1 CCDS46619.1 Transcript intron_variant - - - - - - rs4810142 20:57245425 A 8675 NM_001134772.2 Transcript intron_variant - - - - - - rs4810142 20:57245425 A 8675 NM_003763.5 Transcript intron_variant - - - - - - rs4810142 20:57245425 A 8675 NR_037941.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4810142 20:57245425 A 8675 NR_037942.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4810142 20:57245425 A 8675 NM_001204868.1 Transcript intron_variant - - - - - - rs4810142 20:57245425 A ENSESTG00000026819 ENSESTT00000067706 Transcript intron_variant - - - - - - rs4810142 20:57245425 A ENSESTG00000026819 ENSESTT00000067709 Transcript intron_variant - - - - - - rs4810142 20:57245425 A ENSESTG00000026819 ENSESTT00000067725 Transcript intron_variant - - - - - - rs4810142 20:57245425 A ENSESTG00000026819 ENSESTT00000067676 Transcript intron_variant - - - - - - rs4810142 20:57245425 A CCDS13469.1 CCDS13469.1 Transcript intron_variant - - - - - - rs967478 20:57245894 C 8675 NR_037943.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs967478 20:57245894 C 8675 NM_001134773.2 Transcript intron_variant - - - - - - rs967478 20:57245894 C ENSESTG00000026819 ENSESTT00000067737 Transcript intron_variant - - - - - - rs967478 20:57245894 C CCDS56199.1 CCDS56199.1 Transcript intron_variant - - - - - - rs967478 20:57245894 C CCDS13468.1 CCDS13468.1 Transcript intron_variant - - - - - - rs967478 20:57245894 C CCDS46620.1 CCDS46620.1 Transcript intron_variant - - - - - - rs967478 20:57245894 C 8675 NM_001001433.2 Transcript intron_variant - - - - - - rs967478 20:57245894 C ENSESTG00000027564 ENSESTT00000069378 Transcript upstream_gene_variant - - - - - - DISTANCE=3309 rs967478 20:57245894 C 100534593 NR_037945.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs967478 20:57245894 C CCDS46619.1 CCDS46619.1 Transcript intron_variant - - - - - - rs967478 20:57245894 C 8675 NM_001134772.2 Transcript intron_variant - - - - - - rs967478 20:57245894 C 8675 NM_003763.5 Transcript intron_variant - - - - - - rs967478 20:57245894 C 8675 NR_037941.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs967478 20:57245894 C 8675 NR_037942.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs967478 20:57245894 C 8675 NM_001204868.1 Transcript intron_variant - - - - - - rs967478 20:57245894 C ENSESTG00000026819 ENSESTT00000067706 Transcript intron_variant - - - - - - rs967478 20:57245894 C ENSESTG00000026819 ENSESTT00000067709 Transcript intron_variant - - - - - - rs967478 20:57245894 C ENSESTG00000026819 ENSESTT00000067725 Transcript downstream_gene_variant - - - - - - DISTANCE=295 rs967478 20:57245894 C ENSESTG00000026819 ENSESTT00000067676 Transcript intron_variant - - - - - - rs967478 20:57245894 C CCDS13469.1 CCDS13469.1 Transcript intron_variant - - - - - - rs6015392 20:57451635 G 2778 NM_016592.2 Transcript intron_variant - - - - - - rs6015392 20:57451635 G CCDS46622.1 CCDS46622.1 Transcript intron_variant - - - - - - rs6015392 20:57451635 G 2778 NM_080425.2 Transcript intron_variant - - - - - - rs6015392 20:57451635 G 2778 NM_001077490.1 Transcript intron_variant - - - - - - rs6015392 20:57451635 G ENSESTG00000027000 ENSESTT00000068095 Transcript intron_variant - - - - - - rs862022 20:57602762 T ENSESTG00000027416 ENSESTT00000069201 Transcript downstream_gene_variant - - - - - - DISTANCE=979 rs862022 20:57602762 T CCDS13475.1 CCDS13475.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2924 rs862022 20:57602762 T ENSESTG00000027327 ENSESTT00000068875 Transcript downstream_gene_variant - - - - - - DISTANCE=3613 rs862022 20:57602762 T 100533975 NR_037929.1 Transcript downstream_gene_variant - - - - - - DISTANCE=971 rs862022 20:57602762 T CCDS13476.1 CCDS13476.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2599 rs862022 20:57602762 T 81027 NM_030773.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1053 rs862022 20:57602762 T ENSESTG00000027416 ENSESTT00000069214 Transcript intron_variant - - - - - - rs862022 20:57602762 T ENSESTG00000027416 ENSESTT00000069230 Transcript intron_variant - - - - - - rs862022 20:57602762 T 100533975 NR_037930.1 Transcript downstream_gene_variant - - - - - - DISTANCE=971 rs862022 20:57602762 T ENSESTG00000027416 ENSESTT00000069140 Transcript downstream_gene_variant - - - - - - DISTANCE=985 rs862022 20:57602762 T 514 NM_006886.3 Transcript downstream_gene_variant - - - - - - DISTANCE=971 rs862023 20:57602984 T - ENSR00001450150 RegulatoryFeature regulatory_region_variant - - - - - - rs862023 20:57602984 T ENSESTG00000027416 ENSESTT00000069201 Transcript downstream_gene_variant - - - - - - DISTANCE=757 rs862023 20:57602984 T CCDS13475.1 CCDS13475.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3146 rs862023 20:57602984 T ENSESTG00000027327 ENSESTT00000068875 Transcript downstream_gene_variant - - - - - - DISTANCE=3835 rs862023 20:57602984 T 100533975 NR_037929.1 Transcript downstream_gene_variant - - - - - - DISTANCE=749 rs862023 20:57602984 T CCDS13476.1 CCDS13476.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2377 rs862023 20:57602984 T 81027 NM_030773.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1275 rs862023 20:57602984 T ENSESTG00000027416 ENSESTT00000069214 Transcript intron_variant - - - - - - rs862023 20:57602984 T ENSESTG00000027416 ENSESTT00000069230 Transcript intron_variant - - - - - - rs862023 20:57602984 T 100533975 NR_037930.1 Transcript downstream_gene_variant - - - - - - DISTANCE=749 rs862023 20:57602984 T ENSESTG00000027416 ENSESTT00000069140 Transcript downstream_gene_variant - - - - - - DISTANCE=763 rs862023 20:57602984 T 514 NM_006886.3 Transcript downstream_gene_variant - - - - - - DISTANCE=749 rs236698 20:57674781 T - - - intergenic_variant - - - - - - rs236707 20:57691439 T - - - intergenic_variant - - - - - - rs6100345 20:57712013 C ENSESTG00000027357 ENSESTT00000068893 Transcript intron_variant - - - - - - rs707560 20:57727312 C - - - intergenic_variant - - - - - - rs6015538 20:58213826 G 116154 NM_080672.3 Transcript intron_variant - - - - - - rs6015538 20:58213826 G CCDS56202.1 CCDS56202.1 Transcript intron_variant - - - - - - rs6015538 20:58213826 G ENSESTG00000003514 ENSESTT00000008760 Transcript intron_variant - - - - - - rs6015538 20:58213826 G CCDS13480.1 CCDS13480.1 Transcript intron_variant - - - - - - rs6015538 20:58213826 G ENSESTG00000003514 ENSESTT00000008799 Transcript intron_variant - - - - - - rs6015538 20:58213826 G 116154 NM_001199505.1 Transcript intron_variant - - - - - - rs6015538 20:58213826 G ENSESTG00000003514 ENSESTT00000008795 Transcript intron_variant - - - - - - rs6015538 20:58213826 G ENSESTG00000003514 ENSESTT00000008784 Transcript intron_variant - - - - - - rs6015549 20:58262178 G 116154 NM_080672.3 Transcript intron_variant - - - - - - rs6015549 20:58262178 G ENSESTG00000003514 ENSESTT00000008807 Transcript intron_variant - - - - - - rs6015549 20:58262178 G CCDS56202.1 CCDS56202.1 Transcript intron_variant - - - - - - rs6015549 20:58262178 G ENSESTG00000003514 ENSESTT00000008760 Transcript intron_variant - - - - - - rs6015549 20:58262178 G 116154 NM_001199506.1 Transcript intron_variant - - - - - - rs6015549 20:58262178 G CCDS13480.1 CCDS13480.1 Transcript intron_variant - - - - - - rs6015549 20:58262178 G ENSESTG00000003514 ENSESTT00000008799 Transcript intron_variant - - - - - - rs6015549 20:58262178 G 116154 NM_001199505.1 Transcript intron_variant - - - - - - rs6015549 20:58262178 G ENSESTG00000003514 ENSESTT00000008795 Transcript intron_variant - - - - - - rs6015549 20:58262178 G ENSESTG00000003514 ENSESTT00000008784 Transcript intron_variant - - - - - - rs1321428 20:58263177 A 116154 NM_080672.3 Transcript intron_variant - - - - - - rs1321428 20:58263177 A ENSESTG00000003514 ENSESTT00000008807 Transcript intron_variant - - - - - - rs1321428 20:58263177 A CCDS56202.1 CCDS56202.1 Transcript intron_variant - - - - - - rs1321428 20:58263177 A ENSESTG00000003514 ENSESTT00000008760 Transcript intron_variant - - - - - - rs1321428 20:58263177 A 116154 NM_001199506.1 Transcript intron_variant - - - - - - rs1321428 20:58263177 A CCDS13480.1 CCDS13480.1 Transcript intron_variant - - - - - - rs1321428 20:58263177 A ENSESTG00000003514 ENSESTT00000008799 Transcript intron_variant - - - - - - rs1321428 20:58263177 A 116154 NM_001199505.1 Transcript intron_variant - - - - - - rs1321428 20:58263177 A ENSESTG00000003514 ENSESTT00000008795 Transcript intron_variant - - - - - - rs1321428 20:58263177 A ENSESTG00000003514 ENSESTT00000008784 Transcript intron_variant - - - - - - rs2153169 20:58347914 C 116154 NM_080672.3 Transcript intron_variant - - - - - - rs2153169 20:58347914 C CCDS13481.1 CCDS13481.1 Transcript intron_variant - - - - - - rs2153169 20:58347914 C 116154 NM_183246.1 Transcript intron_variant - - - - - - rs2153169 20:58347914 C ENSESTG00000003514 ENSESTT00000008807 Transcript intron_variant - - - - - - rs2153169 20:58347914 C CCDS42895.1 CCDS42895.1 Transcript intron_variant - - - - - - rs2153169 20:58347914 C CCDS56202.1 CCDS56202.1 Transcript intron_variant - - - - - - rs2153169 20:58347914 C 116154 NM_001199506.1 Transcript intron_variant - - - - - - rs2153169 20:58347914 C CCDS13480.1 CCDS13480.1 Transcript intron_variant - - - - - - rs2153169 20:58347914 C 116154 NM_183244.1 Transcript intron_variant - - - - - - rs2153169 20:58347914 C 116154 NM_001199505.1 Transcript intron_variant - - - - - - rs2153169 20:58347914 C ENSESTG00000003514 ENSESTT00000008784 Transcript intron_variant - - - - - - rs2207969 20:58503985 A 63939 NM_001190826.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4834 rs2207969 20:58503985 A ENSESTG00000003535 ENSESTT00000008849 Transcript upstream_gene_variant - - - - - - DISTANCE=4834 rs2207969 20:58503985 A 10388 NM_014258.2 Transcript intron_variant - - - - - - rs2207969 20:58503985 A ENSESTG00000003606 ENSESTT00000009022 Transcript intron_variant - - - - - - rs2207969 20:58503985 A ENSESTG00000003606 ENSESTT00000009026 Transcript intron_variant - - - - - - rs542035 20:58664103 C ENSESTG00000003581 ENSESTT00000008957 Transcript intron_variant - - - - - - rs542035 20:58664103 C ENSESTG00000003581 ENSESTT00000008969 Transcript intron_variant - - - - - - rs542035 20:58664103 C ENSESTG00000003581 ENSESTT00000008965 Transcript intron_variant - - - - - - rs685937 20:58773048 G 284757 NR_046099.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs242439 20:58782563 G 284757 NR_046099.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4812158 20:58792629 T 284757 NR_046099.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs242437 20:58881443 T 693231 NR_030376.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2089 rs242437 20:58881443 T 284757 NR_046099.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs150797410 20:58889784 T 284757 NR_046099.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs193424 20:59050064 G 100616362 NR_039758.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3105 rs193424 20:59050064 G ENSESTG00000003594 ENSESTT00000008991 Transcript intron_variant - - - - - - rs846217 20:59201220 A - - - intergenic_variant - - - - - - rs846221 20:59223357 A - - - intergenic_variant - - - - - - rs1980800 20:59393055 C - - - intergenic_variant - - - - - - rs6027941 20:59547502 G - - - intergenic_variant - - - - - - rs1407005 20:59695282 G - - - intergenic_variant - - - - - - rs707574 20:59746763 G - - - intergenic_variant - - - - - - rs2427023 20:59854014 G 1002 NM_001794.3 Transcript intron_variant - - - - - - rs2427023 20:59854014 G CCDS13488.1 CCDS13488.1 Transcript intron_variant - - - - - - rs2255222 20:60119061 C 1002 NM_001794.3 Transcript intron_variant - - - - - - rs2255222 20:60119061 C 1002 NM_001252338.1 Transcript intron_variant - - - - - - rs2255222 20:60119061 C CCDS13488.1 CCDS13488.1 Transcript intron_variant - - - - - - rs2798593 20:60153419 C 1002 NM_001794.3 Transcript intron_variant - - - - - - rs2798593 20:60153419 C 1002 NM_001252338.1 Transcript intron_variant - - - - - - rs2798593 20:60153419 C CCDS13488.1 CCDS13488.1 Transcript intron_variant - - - - - - rs6121467 20:60334027 G 1002 NM_001252339.1 Transcript intron_variant - - - - - - rs6121467 20:60334027 G 1002 NM_001794.3 Transcript intron_variant - - - - - - rs6121467 20:60334027 G ENSESTG00000010238 ENSESTT00000025609 Transcript intron_variant - - - - - - rs6121467 20:60334027 G 1002 NM_001252338.1 Transcript intron_variant - - - - - - rs6121467 20:60334027 G CCDS58784.1 CCDS58784.1 Transcript intron_variant - - - - - - rs6121467 20:60334027 G CCDS13488.1 CCDS13488.1 Transcript intron_variant - - - - - - rs6121812 20:60381699 C 1002 NM_001252339.1 Transcript intron_variant - - - - - - rs6121812 20:60381699 C 1002 NM_001794.3 Transcript intron_variant - - - - - - rs6121812 20:60381699 C 1002 NM_001252338.1 Transcript intron_variant - - - - - - rs6121812 20:60381699 C CCDS58784.1 CCDS58784.1 Transcript intron_variant - - - - - - rs6121812 20:60381699 C CCDS13488.1 CCDS13488.1 Transcript intron_variant - - - - - - rs6061942 20:60556957 C - ENSR00000403987 RegulatoryFeature regulatory_region_variant - - - - - - rs6061942 20:60556957 C ENSESTG00000010557 ENSESTT00000026456 Transcript upstream_gene_variant - - - - - - DISTANCE=2880 rs6061942 20:60556957 C CCDS33500.1 CCDS33500.1 Transcript intron_variant - - - - - - rs6061942 20:60556957 C ENSESTG00000010557 ENSESTT00000026444 Transcript intron_variant - - - - - - rs6061942 20:60556957 C ENSESTG00000010557 ENSESTT00000026439 Transcript intron_variant - - - - - - rs6061942 20:60556957 C 6874 NM_003185.3 Transcript intron_variant - - - - - - rs2057477 20:60620024 C CCDS33500.1 CCDS33500.1 Transcript intron_variant - - - - - - rs2057477 20:60620024 C 6874 NM_003185.3 Transcript intron_variant - - - - - - rs2427279 20:60883919 C CCDS13496.1 CCDS13496.1 Transcript downstream_gene_variant - - - - - - DISTANCE=102 rs2427279 20:60883919 C ENSESTG00000010388 ENSESTT00000026056 Transcript downstream_gene_variant - - - - - - DISTANCE=4117 rs2427279 20:60883919 C 3911 NM_005560.3 Transcript downstream_gene_variant - - - - - - DISTANCE=202 rs2427279 20:60883919 C ENSESTG00000010388 ENSESTT00000026047 Transcript downstream_gene_variant - - - - - - DISTANCE=3 rs2427279 20:60883919 C ENSESTG00000010388 ENSESTT00000026054 Transcript downstream_gene_variant - - - - - - DISTANCE=474 rs2427279 20:60883919 C CCDS33502.1 CCDS33502.1 Transcript downstream_gene_variant - - - - - - DISTANCE=473 rs2427279 20:60883919 C ENSESTG00000010388 ENSESTT00000026010 Transcript downstream_gene_variant - - - - - - DISTANCE=2 rs2427279 20:60883919 C ENSESTG00000010517 ENSESTT00000026304 Transcript upstream_gene_variant - - - - - - DISTANCE=1529 rs2427279 20:60883919 C 11047 NM_007002.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1 rs2427279 20:60883919 C 11047 NM_175573.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1 rs28373313 20:61206654 C - - - intergenic_variant - - - - - - rs2224311 20:61709245 T 63930 NR_033370.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2224311 20:61709245 T ENSESTG00000029232 ENSESTT00000073643 Transcript intron_variant - - - - - - rs2224311 20:61709245 T ENSESTG00000029232 ENSESTT00000073628 Transcript intron_variant - - - - - - rs6011815 20:62035183 G CCDS13518.1 CCDS13518.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2814 rs6011815 20:62035183 G ENSESTG00000029704 ENSESTT00000074727 Transcript downstream_gene_variant - - - - - - DISTANCE=3288 rs6011815 20:62035183 G CCDS13520.1 CCDS13520.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2814 rs6011815 20:62035183 G 3785 NM_172106.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2359 rs6011815 20:62035183 G 3785 NM_172108.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2359 rs6011815 20:62035183 G 3785 NM_004518.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2359 rs6011815 20:62035183 G CCDS46629.1 CCDS46629.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2814 rs6011815 20:62035183 G ENSESTG00000029648 ENSESTT00000074598 Transcript downstream_gene_variant - - - - - - DISTANCE=1250 rs6011815 20:62035183 G CCDS13519.1 CCDS13519.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2814 rs6011815 20:62035183 G 3785 NM_172107.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2359 rs2244283 20:62543326 C ENSESTG00000000090 ENSESTT00000000252 Transcript intron_variant - - - - - - rs2244283 20:62543326 C 80331 NM_025219.2 Transcript intron_variant - - - - - - rs2244283 20:62543326 C ENSESTG00000000090 ENSESTT00000000256 Transcript intron_variant - - - - - - rs2244283 20:62543326 C ENSESTG00000000090 ENSESTT00000000255 Transcript intron_variant - - - - - - rs2244283 20:62543326 C ENSESTG00000000090 ENSESTT00000000247 Transcript intron_variant - - - - - - rs212134 21:10931669 A ENSESTG00000010490 ENSESTT00000026281 Transcript intron_variant - - - - - - rs212134 21:10931669 A 7179 NM_199261.2 Transcript intron_variant - - - - - - rs212134 21:10931669 A ENSESTG00000010490 ENSESTT00000026295 Transcript intron_variant - - - - - - rs212134 21:10931669 A ENSESTG00000010490 ENSESTT00000026278 Transcript intron_variant - - - - - - rs212134 21:10931669 A 7179 NM_199259.2 Transcript intron_variant - - - - - - rs212134 21:10931669 A CCDS33512.1 CCDS33512.1 Transcript intron_variant - - - - - - rs212134 21:10931669 A 7179 NM_199260.2 Transcript intron_variant - - - - - - rs212134 21:10931669 A ENSESTG00000010490 ENSESTT00000026289 Transcript intron_variant - - - - - - rs212134 21:10931669 A CCDS13560.2 CCDS13560.2 Transcript intron_variant - - - - - - rs212134 21:10931669 A CCDS33511.1 CCDS33511.1 Transcript intron_variant - - - - - - rs467885 21:10969606 A ENSESTG00000010490 ENSESTT00000026281 Transcript intron_variant - - - - - - rs467885 21:10969606 A 7179 NM_199261.2 Transcript intron_variant - - - - - - rs467885 21:10969606 A ENSESTG00000010490 ENSESTT00000026295 Transcript intron_variant - - - - - - rs467885 21:10969606 A ENSESTG00000010490 ENSESTT00000026278 Transcript intron_variant - - - - - - rs467885 21:10969606 A 7179 NM_199259.2 Transcript intron_variant - - - - - - rs467885 21:10969606 A CCDS33512.1 CCDS33512.1 Transcript intron_variant - - - - - - rs467885 21:10969606 A 7179 NM_199260.2 Transcript intron_variant - - - - - - rs467885 21:10969606 A ENSESTG00000010490 ENSESTT00000026289 Transcript intron_variant - - - - - - rs467885 21:10969606 A CCDS13560.2 CCDS13560.2 Transcript intron_variant - - - - - - rs467885 21:10969606 A CCDS33511.1 CCDS33511.1 Transcript intron_variant - - - - - - rs469825 21:11136689 T - - - intergenic_variant - - - - - - rs239272 21:14398825 G ENSESTG00000005442 ENSESTT00000013827 Transcript intron_variant - - - - - - rs7276452 21:14942432 T - - - intergenic_variant - - - - - - rs1297099 21:15382486 G - - - intergenic_variant - - - - - - rs1297108 21:15392106 C - - - intergenic_variant - - - - - - rs28398154 21:15444282 A ENSESTG00000019542 ENSESTT00000049057 Transcript intron_variant - - - - - - rs7283442 21:15516976 A ENSESTG00000019542 ENSESTT00000049088 Transcript downstream_gene_variant - - - - - - DISTANCE=200 rs7283442 21:15516976 A ENSESTG00000019653 ENSESTT00000049293 Transcript missense_variant 615 483 161 R/S agA/agT - rs7283442 21:15516976 A CCDS13564.1 CCDS13564.1 Transcript missense_variant 1326 1326 442 R/S agA/agT - PolyPhen=benign;SIFT=tolerated rs7283442 21:15516976 A 149998 NM_198996.2 Transcript missense_variant 1336 1326 442 R/S agA/agT - PolyPhen=benign;SIFT=tolerated rs1297139 21:15580607 G ENSESTG00000019643 ENSESTT00000049262 Transcript upstream_gene_variant - - - - - - DISTANCE=1337 rs1297139 21:15580607 G CCDS13564.1 CCDS13564.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1363 rs1297139 21:15580607 G 149998 NM_198996.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1353 rs1297140 21:15593037 G ENSESTG00000019579 ENSESTT00000049201 Transcript intron_variant - - - - - - rs1297140 21:15593037 G ENSESTG00000019579 ENSESTT00000049189 Transcript intron_variant - - - - - - rs1297140 21:15593037 G ENSESTG00000019579 ENSESTT00000049145 Transcript intron_variant - - - - - - rs1297140 21:15593037 G CCDS46635.1 CCDS46635.1 Transcript intron_variant - - - - - - rs1297140 21:15593037 G 54033 NM_144770.3 Transcript intron_variant - - - - - - rs1297141 21:15609891 C - - - intergenic_variant - - - - - - rs1297142 21:15612287 T - - - intergenic_variant - - - - - - rs1739488 21:15614750 G - - - intergenic_variant - - - - - - rs1739489 21:15614753 G - - - intergenic_variant - - - - - - rs1297143 21:15625771 C - - - intergenic_variant - - - - - - rs1297144 21:15628412 G - - - intergenic_variant - - - - - - rs1297145 21:15628651 G - - - intergenic_variant - - - - - - rs1153301 21:15641328 G ENSESTG00000019621 ENSESTT00000049231 Transcript upstream_gene_variant - - - - - - DISTANCE=4787 rs1153301 21:15641328 G 150000 NR_003088.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4792 rs1153301 21:15641328 G 150000 NR_003087.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4792 rs1153302 21:15641426 C ENSESTG00000019621 ENSESTT00000049231 Transcript upstream_gene_variant - - - - - - DISTANCE=4689 rs1153302 21:15641426 C 150000 NR_003088.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4694 rs1153302 21:15641426 C 150000 NR_003087.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4694 rs1153332 21:15685826 A - - - intergenic_variant - - - - - - rs7275771 21:15841550 A - - - intergenic_variant - - - - - - rs365709 21:15878599 A ENSESTG00000023208 ENSESTT00000058684 Transcript intron_variant - - - - - - rs365709 21:15878599 A CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs365709 21:15878599 A CCDS42906.1 CCDS42906.1 Transcript intron_variant - - - - - - rs365709 21:15878599 A 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs365709 21:15878599 A 64092 NM_022136.4 Transcript intron_variant - - - - - - rs365709 21:15878599 A ENSESTG00000023208 ENSESTT00000058696 Transcript intron_variant - - - - - - rs11700991 21:15888430 C ENSESTG00000023208 ENSESTT00000058684 Transcript intron_variant - - - - - - rs11700991 21:15888430 C CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs11700991 21:15888430 C 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs11700991 21:15888430 C 64092 NM_022136.4 Transcript intron_variant - - - - - - rs11700991 21:15888430 C ENSESTG00000023208 ENSESTT00000058711 Transcript intron_variant - - - - - - rs11700991 21:15888430 C ENSESTG00000023208 ENSESTT00000058705 Transcript intron_variant - - - - - - rs11700991 21:15888430 C CCDS42906.1 CCDS42906.1 Transcript intron_variant - - - - - - rs11700991 21:15888430 C ENSESTG00000023208 ENSESTT00000058696 Transcript intron_variant - - - - - - rs7282308 21:15895459 G ENSESTG00000023208 ENSESTT00000058684 Transcript intron_variant - - - - - - rs7282308 21:15895459 G CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs7282308 21:15895459 G 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs7282308 21:15895459 G 64092 NM_022136.4 Transcript intron_variant - - - - - - rs7282308 21:15895459 G ENSESTG00000023208 ENSESTT00000058711 Transcript intron_variant - - - - - - rs7282308 21:15895459 G ENSESTG00000023208 ENSESTT00000058705 Transcript intron_variant - - - - - - rs7282308 21:15895459 G CCDS42906.1 CCDS42906.1 Transcript intron_variant - - - - - - rs7282308 21:15895459 G ENSESTG00000023208 ENSESTT00000058696 Transcript intron_variant - - - - - - rs2142311 21:15901716 C ENSESTG00000023208 ENSESTT00000058684 Transcript intron_variant - - - - - - rs2142311 21:15901716 C CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs2142311 21:15901716 C 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs2142311 21:15901716 C 64092 NM_022136.4 Transcript intron_variant - - - - - - rs2142311 21:15901716 C ENSESTG00000023208 ENSESTT00000058711 Transcript intron_variant - - - - - - rs2142311 21:15901716 C ENSESTG00000023208 ENSESTT00000058705 Transcript intron_variant - - - - - - rs2142311 21:15901716 C CCDS42906.1 CCDS42906.1 Transcript intron_variant - - - - - - rs2142311 21:15901716 C ENSESTG00000023208 ENSESTT00000058696 Transcript intron_variant - - - - - - rs6516874 21:15923715 C CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs6516874 21:15923715 C 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs8128986 21:15924887 G CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs8128986 21:15924887 G 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs2142313 21:15925318 C CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs2142313 21:15925318 C 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs1882915 21:15930775 G CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs1882915 21:15930775 G 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs6516884 21:15939510 G - ENSR00000315472 RegulatoryFeature regulatory_region_variant - - - - - - rs6516884 21:15939510 G CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs6516884 21:15939510 G 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs926145 21:15949925 T CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs926145 21:15949925 T 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs926145 21:15949925 T 100874190 NR_046512.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4598 rs4817265 21:15951404 G CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs4817265 21:15951404 G 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs4817265 21:15951404 G 100874190 NR_046512.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3119 rs4817268 21:15951528 C CCDS58786.1 CCDS58786.1 Transcript intron_variant - - - - - - rs4817268 21:15951528 C 64092 NM_001256370.1 Transcript intron_variant - - - - - - rs4817268 21:15951528 C 100874190 NR_046512.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2995 rs465516 21:15970405 A ENSESTG00000023155 ENSESTT00000058497 Transcript intron_variant - - - - - - rs465516 21:15970405 A ENSESTG00000023155 ENSESTT00000058514 Transcript intron_variant - - - - - - rs465516 21:15970405 A 388813 NM_001256579.1 Transcript intron_variant - - - - - - rs465516 21:15970405 A 100874190 NR_046512.1 Transcript non_coding_exon_variant,nc_transcript_variant 621 - - - - - rs456067 21:15974409 C ENSESTG00000023155 ENSESTT00000058497 Transcript missense_variant 384 334 112 N/D Aat/Gat - PolyPhen=benign rs456067 21:15974409 C ENSESTG00000023155 ENSESTT00000058514 Transcript missense_variant 284 250 84 N/D Aat/Gat - rs456067 21:15974409 C 388813 NM_001256579.1 Transcript missense_variant 284 250 84 N/D Aat/Gat - rs456067 21:15974409 C 100874190 NR_046512.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3785 rs1292584 21:15986972 A ENSESTG00000023155 ENSESTT00000058497 Transcript intron_variant - - - - - - rs1292584 21:15986972 A ENSESTG00000023155 ENSESTT00000058514 Transcript intron_variant - - - - - - rs1292584 21:15986972 A 388813 NM_001256579.1 Transcript intron_variant - - - - - - rs466592 21:16022391 A ENSESTG00000023155 ENSESTT00000058497 Transcript intron_variant - - - - - - rs1292736 21:16104232 G - - - intergenic_variant - - - - - - rs7275617 21:16198965 C - ENSR00000611434 RegulatoryFeature regulatory_region_variant - - - - - - rs7275617 21:16198965 C ENSESTG00000023149 ENSESTT00000058442 Transcript intron_variant - - - - - - rs909384 21:16214054 G - ENSR00001565477 RegulatoryFeature regulatory_region_variant - - - - - - rs909384 21:16214054 G ENSESTG00000023149 ENSESTT00000058442 Transcript upstream_gene_variant - - - - - - DISTANCE=4657 rs2210219 21:16217998 C - - - intergenic_variant - - - - - - rs2205535 21:16228651 T - - - intergenic_variant - - - - - - rs1554996 21:16229159 C - - - intergenic_variant - - - - - - rs9305476 21:16232889 G - - - intergenic_variant - - - - - - rs2403839 21:16253266 G - ENSR00000611443 RegulatoryFeature regulatory_region_variant - - - - - - rs2403839 21:16253266 G - - - intergenic_variant - - - - - - rs6517081 21:16258979 G - - - intergenic_variant - - - - - - rs7276189 21:16265597 T - - - intergenic_variant - - - - - - rs7283682 21:16265669 A - - - intergenic_variant - - - - - - rs9980868 21:16265817 T - - - intergenic_variant - - - - - - rs959251 21:16267856 A - - - intergenic_variant - - - - - - rs7281898 21:16275824 T - - - intergenic_variant - - - - - - rs2736078 21:16446591 G - - - intergenic_variant - - - - - - rs2223049 21:16659256 G - - - intergenic_variant - - - - - - rs1736139 21:16769452 T ENSESTG00000014942 ENSESTT00000037416 Transcript downstream_gene_variant - - - - - - DISTANCE=3346 rs1297249 21:16769606 G ENSESTG00000014942 ENSESTT00000037416 Transcript downstream_gene_variant - - - - - - DISTANCE=3192 rs7283677 21:17427619 G - - - intergenic_variant - - - - - - rs2105697 21:17463756 T 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2105697 21:17463756 T ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs2105697 21:17463756 T ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs6517688 21:17480935 C - ENSR00001565588 RegulatoryFeature regulatory_region_variant - - - - - - rs6517688 21:17480935 C 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6517688 21:17480935 C ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs6517688 21:17480935 C ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs6517691 21:17533418 A 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6517691 21:17533418 A ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs6517691 21:17533418 A ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs171189 21:17584835 A 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs171189 21:17584835 A ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs171189 21:17584835 A ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs171189 21:17584835 A 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs171189 21:17584835 A ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs2639699 21:17590360 A 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2639699 21:17590360 A ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs2639699 21:17590360 A ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs2639699 21:17590360 A 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2639699 21:17590360 A ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs238989 21:17616912 T 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs238989 21:17616912 T ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs238989 21:17616912 T ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs238989 21:17616912 T 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs238989 21:17616912 T ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs239045 21:17653310 T - ENSR00000611624 RegulatoryFeature regulatory_region_variant - - - - - - rs239045 21:17653310 T 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239045 21:17653310 T ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs239045 21:17653310 T ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs239045 21:17653310 T 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239045 21:17653310 T ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs239046 21:17653703 C 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239046 21:17653703 C ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs239046 21:17653703 C ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs239046 21:17653703 C 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239046 21:17653703 C ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs239061 21:17664085 C 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239061 21:17664085 C ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs239061 21:17664085 C ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs239061 21:17664085 C 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239061 21:17664085 C ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs239016 21:17698140 A 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239016 21:17698140 A ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs239016 21:17698140 A ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs239016 21:17698140 A 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239016 21:17698140 A ENSESTG00000017674 ENSESTT00000044562 Transcript upstream_gene_variant - - - - - - DISTANCE=4785 rs239016 21:17698140 A ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs239012 21:17715421 C 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239012 21:17715421 C ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs239012 21:17715421 C ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs239012 21:17715421 C 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs239012 21:17715421 C ENSESTG00000017674 ENSESTT00000044562 Transcript intron_variant - - - - - - rs239012 21:17715421 C ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs240454 21:17788155 A ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs240454 21:17788155 A ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs240454 21:17788155 A ENSESTG00000017674 ENSESTT00000044595 Transcript upstream_gene_variant - - - - - - DISTANCE=3597 rs240454 21:17788155 A ENSESTG00000017674 ENSESTT00000044562 Transcript intron_variant - - - - - - rs240454 21:17788155 A ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs240454 21:17788155 A 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs240454 21:17788155 A 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs240454 21:17788155 A ENSESTG00000017674 ENSESTT00000044614 Transcript upstream_gene_variant - - - - - - DISTANCE=3683 rs240454 21:17788155 A ENSESTG00000017674 ENSESTT00000044587 Transcript upstream_gene_variant - - - - - - DISTANCE=3493 rs240452 21:17791840 C - ENSR00001565609 RegulatoryFeature regulatory_region_variant - - - - - - rs240452 21:17791840 C ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs240452 21:17791840 C ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs240452 21:17791840 C ENSESTG00000017674 ENSESTT00000044595 Transcript 5_prime_UTR_variant 89 - - - - - rs240452 21:17791840 C ENSESTG00000017674 ENSESTT00000044562 Transcript intron_variant - - - - - - rs240452 21:17791840 C ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs240452 21:17791840 C 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs240452 21:17791840 C 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs240452 21:17791840 C ENSESTG00000017674 ENSESTT00000044614 Transcript 5_prime_UTR_variant 3 - - - - - rs240452 21:17791840 C ENSESTG00000017674 ENSESTT00000044587 Transcript 5_prime_UTR_variant 193 - - - - - rs240451 21:17791847 T - ENSR00001565609 RegulatoryFeature regulatory_region_variant - - - - - - rs240451 21:17791847 T ENSESTG00000014913 ENSESTT00000037387 Transcript intron_variant - - - - - - rs240451 21:17791847 T ENSESTG00000014913 ENSESTT00000037369 Transcript intron_variant - - - - - - rs240451 21:17791847 T ENSESTG00000017674 ENSESTT00000044595 Transcript 5_prime_UTR_variant 96 - - - - - rs240451 21:17791847 T ENSESTG00000017674 ENSESTT00000044562 Transcript intron_variant - - - - - - rs240451 21:17791847 T ENSESTG00000014913 ENSESTT00000037378 Transcript intron_variant - - - - - - rs240451 21:17791847 T 388815 NR_027790.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs240451 21:17791847 T 388815 NR_027791.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs240451 21:17791847 T ENSESTG00000017674 ENSESTT00000044614 Transcript 5_prime_UTR_variant 10 - - - - - rs240451 21:17791847 T ENSESTG00000017674 ENSESTT00000044587 Transcript 5_prime_UTR_variant 200 - - - - - rs2736249 21:18134277 A - - - intergenic_variant - - - - - - rs12626793 21:18135286 C - - - intergenic_variant - - - - - - rs4818283 21:18135594 A - - - intergenic_variant - - - - - - rs2223067 21:18160862 A - - - intergenic_variant - - - - - - rs9976144 21:18172324 C - - - intergenic_variant - - - - - - rs9305784 21:18172625 C - - - intergenic_variant - - - - - - rs8134865 21:18183327 C - - - intergenic_variant - - - - - - rs8126593 21:18183482 C - - - intergenic_variant - - - - - - rs1034119 21:18196781 C - - - intergenic_variant - - - - - - rs979046 21:18222334 C - - - intergenic_variant - - - - - - rs7275939 21:18222435 G - - - intergenic_variant - - - - - - rs7278685 21:18284432 C - ENSR00001565651 RegulatoryFeature regulatory_region_variant - - - - - - rs7278685 21:18284432 C - - - intergenic_variant - - - - - - rs1297528 21:18379660 A - - - intergenic_variant - - - - - - rs2205323 21:18441021 A - - - intergenic_variant - - - - - - rs3891152 21:18535049 A - - - intergenic_variant - - - - - - rs202893 21:18585760 A - - - intergenic_variant - - - - - - rs2211956 21:18594331 A - - - intergenic_variant - - - - - - rs207014 21:18639491 A - - - intergenic_variant - - - - - - rs207015 21:18642911 C - ENSR00000683991 RegulatoryFeature regulatory_region_variant - - - - - - rs207015 21:18642911 C - - - intergenic_variant - - - - - - rs207016 21:18643246 A - - - intergenic_variant - - - - - - rs2849882 21:18652444 T - - - intergenic_variant - - - - - - rs1907978 21:18694201 C - - - intergenic_variant - - - - - - rs2101803 21:18991477 G - - - intergenic_variant - - - - - - rs169837 21:18993466 A - - - intergenic_variant - - - - - - rs79821168 21:19064647 A - - - intergenic_variant - - - - - - rs243633 21:19100432 C - - - intergenic_variant - - - - - - rs243634 21:19101314 T - - - intergenic_variant - - - - - - rs243641 21:19106990 A - - - intergenic_variant - - - - - - rs557965 21:19115285 T - ENSR00000611758 RegulatoryFeature regulatory_region_variant - - - - - - rs557965 21:19115285 T - - - intergenic_variant - - - - - - rs243615 21:19203998 G 54075 NR_024354.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3991 rs243610 21:19247378 T ENSESTG00000014354 ENSESTT00000035905 Transcript intron_variant - - - - - - rs243610 21:19247378 T 54075 NR_024354.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9305830 21:19262017 G ENSESTG00000014354 ENSESTT00000035905 Transcript upstream_gene_variant - - - - - - DISTANCE=4092 rs9305830 21:19262017 G 54075 NR_024354.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4092 rs2205377 21:19289744 C - - - intergenic_variant - - - - - - rs7283378 21:19299293 A - - - intergenic_variant - - - - - - rs149787 21:19344589 G - - - intergenic_variant - - - - - - rs197574 21:19347686 C - - - intergenic_variant - - - - - - rs149789 21:19347838 C - - - intergenic_variant - - - - - - rs197579 21:19350443 G - - - intergenic_variant - - - - - - rs197521 21:19413994 T 140578 NM_001204176.1 Transcript intron_variant - - - - - - rs197521 21:19413994 T 140578 NM_001204178.1 Transcript intron_variant - - - - - - rs204010 21:19459215 G 140578 NM_001204176.1 Transcript intron_variant - - - - - - rs204010 21:19459215 G 140578 NM_001204178.1 Transcript intron_variant - - - - - - rs204007 21:19461260 G 140578 NM_001204176.1 Transcript intron_variant - - - - - - rs204007 21:19461260 G 140578 NM_001204178.1 Transcript intron_variant - - - - - - rs150347 21:19461501 G 140578 NM_001204176.1 Transcript intron_variant - - - - - - rs150347 21:19461501 G 140578 NM_001204178.1 Transcript intron_variant - - - - - - rs1688151 21:19464401 C 140578 NM_001204176.1 Transcript intron_variant - - - - - - rs1688151 21:19464401 C 140578 NM_001204178.1 Transcript intron_variant - - - - - - rs2406168 21:19519570 C 140578 NM_001204176.1 Transcript intron_variant - - - - - - rs2406168 21:19519570 C 140578 NM_001204178.1 Transcript intron_variant - - - - - - rs8133856 21:19540441 C 140578 NM_001204176.1 Transcript intron_variant - - - - - - rs8133856 21:19540441 C 140578 NM_001204178.1 Transcript intron_variant - - - - - - rs3859709 21:19688173 T CCDS13571.1 CCDS13571.1 Transcript intron_variant - - - - - - rs3859709 21:19688173 T 5651 NM_002772.2 Transcript intron_variant - - - - - - rs9647202 21:19803037 T - - - intergenic_variant - - - - - - rs6517816 21:19937015 T - - - intergenic_variant - - - - - - rs7276526 21:20031352 A ENSESTG00000007036 ENSESTT00000017824 Transcript intron_variant - - - - - - rs7283735 21:20143958 T - - - intergenic_variant - - - - - - rs1539949 21:20200221 T - - - intergenic_variant - - - - - - rs2000483 21:20431578 C - - - intergenic_variant - - - - - - rs995440 21:20437058 G - - - intergenic_variant - - - - - - rs11911270 21:20496937 A - - - intergenic_variant - - - - - - rs9979296 21:20504399 C - - - intergenic_variant - - - - - - rs7282790 21:20593062 T - - - intergenic_variant - - - - - - rs2211940 21:20595702 C - - - intergenic_variant - - - - - - rs2186767 21:20629003 T - - - intergenic_variant - - - - - - rs1491648 21:20818402 T - - - intergenic_variant - - - - - - rs427922 21:20893840 A - - - intergenic_variant - - - - - - rs419520 21:20897329 T - - - intergenic_variant - - - - - - rs8129546 21:21044853 A - - - intergenic_variant - - - - - - rs7281822 21:21049828 T - - - intergenic_variant - - - - - - rs704569 21:21072685 T - - - intergenic_variant - - - - - - rs2776094 21:21076546 C - - - intergenic_variant - - - - - - rs218337 21:21086178 A - - - intergenic_variant - - - - - - rs1518253 21:21097398 A - - - intergenic_variant - - - - - - rs765355 21:21193088 T - - - intergenic_variant - - - - - - rs1153403 21:21417257 C - - - intergenic_variant - - - - - - rs1228705 21:21609705 T - - - intergenic_variant - - - - - - rs2087227 21:21610121 C - - - intergenic_variant - - - - - - rs1487936 21:21722040 A - - - intergenic_variant - - - - - - rs1487937 21:21722516 T - - - intergenic_variant - - - - - - rs9977096 21:21737710 G - - - intergenic_variant - - - - - - rs915794 21:21744413 C - - - intergenic_variant - - - - - - rs2008902 21:21745240 C - - - intergenic_variant - - - - - - rs4327303 21:21751797 G - - - intergenic_variant - - - - - - rs2032199 21:21759796 C - - - intergenic_variant - - - - - - rs9305957 21:21761011 G - ENSR00000611847 RegulatoryFeature regulatory_region_variant - - - - - - rs9305957 21:21761011 G - - - intergenic_variant - - - - - - rs2178987 21:21781501 C ENSESTG00000005974 ENSESTT00000015136 Transcript intron_variant - - - - - - rs2103495 21:21782124 G ENSESTG00000005974 ENSESTT00000015136 Transcript intron_variant - - - - - - rs9984000 21:21784582 C ENSESTG00000005974 ENSESTT00000015136 Transcript intron_variant - - - - - - rs9981762 21:21784719 G ENSESTG00000005974 ENSESTT00000015136 Transcript intron_variant - - - - - - rs7282737 21:21788788 G ENSESTG00000005974 ENSESTT00000015136 Transcript intron_variant - - - - - - rs2223145 21:21792571 C ENSESTG00000005974 ENSESTT00000015136 Transcript intron_variant - - - - - - rs4818569 21:21792688 G ENSESTG00000005974 ENSESTT00000015136 Transcript intron_variant - - - - - - rs962114 21:21819911 A - - - intergenic_variant - - - - - - rs7278943 21:21862618 T - - - intergenic_variant - - - - - - rs2065244 21:21956271 A - - - intergenic_variant - - - - - - rs229412 21:21994280 G - - - intergenic_variant - - - - - - rs2212879 21:22029688 G ENSESTG00000006018 ENSESTT00000015248 Transcript intron_variant - - - - - - rs6518079 21:22477975 C 4685 NM_004540.3 Transcript intron_variant - - - - - - rs6518079 21:22477975 C CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs7279647 21:22504105 T 4685 NM_004540.3 Transcript intron_variant - - - - - - rs7279647 21:22504105 T CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs13046539 21:22605588 A 4685 NM_004540.3 Transcript intron_variant - - - - - - rs13046539 21:22605588 A CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs13046539 21:22605588 A ENSESTG00000005976 ENSESTT00000015157 Transcript intron_variant - - - - - - rs13046539 21:22605588 A ENSESTG00000005976 ENSESTT00000015151 Transcript intron_variant - - - - - - rs7276408 21:22703743 C 4685 NM_004540.3 Transcript intron_variant - - - - - - rs7276408 21:22703743 C CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs7276408 21:22703743 C ENSESTG00000008085 ENSESTT00000020500 Transcript intron_variant - - - - - - rs7276408 21:22703743 C ENSESTG00000008085 ENSESTT00000020497 Transcript intron_variant - - - - - - rs7276408 21:22703743 C ENSESTG00000008085 ENSESTT00000020496 Transcript intron_variant - - - - - - rs7276408 21:22703743 C ENSESTG00000008085 ENSESTT00000020488 Transcript intron_variant - - - - - - rs7276408 21:22703743 C ENSESTG00000008085 ENSESTT00000020491 Transcript intron_variant - - - - - - rs7276408 21:22703743 C ENSESTG00000008085 ENSESTT00000020498 Transcript intron_variant - - - - - - rs7276408 21:22703743 C ENSESTG00000008085 ENSESTT00000020446 Transcript intron_variant - - - - - - rs2588655 21:22734450 G 4685 NM_004540.3 Transcript intron_variant - - - - - - rs2588655 21:22734450 G CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs2588655 21:22734450 G ENSESTG00000008085 ENSESTT00000020500 Transcript intron_variant - - - - - - rs2588655 21:22734450 G ENSESTG00000008085 ENSESTT00000020497 Transcript intron_variant - - - - - - rs2588655 21:22734450 G ENSESTG00000008085 ENSESTT00000020496 Transcript intron_variant - - - - - - rs2588655 21:22734450 G ENSESTG00000008085 ENSESTT00000020488 Transcript intron_variant - - - - - - rs2588655 21:22734450 G ENSESTG00000008085 ENSESTT00000020491 Transcript intron_variant - - - - - - rs2588655 21:22734450 G ENSESTG00000008085 ENSESTT00000020498 Transcript intron_variant - - - - - - rs232428 21:22757583 C 4685 NM_004540.3 Transcript intron_variant - - - - - - rs232428 21:22757583 C CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs232428 21:22757583 C ENSESTG00000008085 ENSESTT00000020500 Transcript intron_variant - - - - - - rs232428 21:22757583 C ENSESTG00000008085 ENSESTT00000020497 Transcript intron_variant - - - - - - rs232428 21:22757583 C ENSESTG00000008085 ENSESTT00000020496 Transcript intron_variant - - - - - - rs232428 21:22757583 C ENSESTG00000008085 ENSESTT00000020488 Transcript intron_variant - - - - - - rs232428 21:22757583 C ENSESTG00000008085 ENSESTT00000020491 Transcript intron_variant - - - - - - rs232428 21:22757583 C ENSESTG00000008085 ENSESTT00000020498 Transcript intron_variant - - - - - - rs232402 21:22805384 G 4685 NM_004540.3 Transcript intron_variant - - - - - - rs232402 21:22805384 G CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs232402 21:22805384 G ENSESTG00000008085 ENSESTT00000020500 Transcript downstream_gene_variant - - - - - - DISTANCE=662 rs232402 21:22805384 G ENSESTG00000008085 ENSESTT00000020497 Transcript intron_variant - - - - - - rs232402 21:22805384 G ENSESTG00000008085 ENSESTT00000020496 Transcript downstream_gene_variant - - - - - - DISTANCE=662 rs232402 21:22805384 G ENSESTG00000008085 ENSESTT00000020488 Transcript intron_variant - - - - - - rs232402 21:22805384 G ENSESTG00000008085 ENSESTT00000020491 Transcript intron_variant - - - - - - rs232402 21:22805384 G ENSESTG00000008085 ENSESTT00000020498 Transcript intron_variant - - - - - - rs232403 21:22807828 G 4685 NM_004540.3 Transcript intron_variant - - - - - - rs232403 21:22807828 G CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs232403 21:22807828 G ENSESTG00000008085 ENSESTT00000020500 Transcript downstream_gene_variant - - - - - - DISTANCE=3106 rs232403 21:22807828 G ENSESTG00000008085 ENSESTT00000020497 Transcript intron_variant - - - - - - rs232403 21:22807828 G ENSESTG00000008085 ENSESTT00000020496 Transcript downstream_gene_variant - - - - - - DISTANCE=3106 rs232403 21:22807828 G ENSESTG00000008085 ENSESTT00000020488 Transcript intron_variant - - - - - - rs232403 21:22807828 G ENSESTG00000008085 ENSESTT00000020491 Transcript intron_variant - - - - - - rs232403 21:22807828 G ENSESTG00000008085 ENSESTT00000020498 Transcript intron_variant - - - - - - rs233792 21:22829500 A 4685 NM_004540.3 Transcript intron_variant - - - - - - rs233792 21:22829500 A CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs233792 21:22829500 A ENSESTG00000008085 ENSESTT00000020488 Transcript intron_variant - - - - - - rs233792 21:22829500 A ENSESTG00000008085 ENSESTT00000020498 Transcript intron_variant - - - - - - rs233792 21:22829500 A ENSESTG00000008085 ENSESTT00000020497 Transcript intron_variant - - - - - - rs233792 21:22829500 A ENSESTG00000008085 ENSESTT00000020491 Transcript intron_variant - - - - - - rs233802 21:22885240 T 4685 NM_004540.3 Transcript intron_variant - - - - - - rs233802 21:22885240 T CCDS42910.1 CCDS42910.1 Transcript intron_variant - - - - - - rs233802 21:22885240 T ENSESTG00000008085 ENSESTT00000020488 Transcript intron_variant - - - - - - rs233802 21:22885240 T ENSESTG00000008085 ENSESTT00000020497 Transcript intron_variant - - - - - - rs180474 21:22944018 A ENSESTG00000008122 ENSESTT00000020513 Transcript intron_variant - - - - - - rs236048 21:22947712 G ENSESTG00000008122 ENSESTT00000020513 Transcript intron_variant - - - - - - rs1156104 21:22982947 T ENSESTG00000008122 ENSESTT00000020513 Transcript intron_variant - - - - - - rs1736002 21:23065121 T - - - intergenic_variant - - - - - - rs1735713 21:23068012 G - - - intergenic_variant - - - - - - rs1735714 21:23068019 G - - - intergenic_variant - - - - - - rs1735978 21:23134187 T - - - intergenic_variant - - - - - - rs1735988 21:23136975 T - - - intergenic_variant - - - - - - rs932942 21:23167183 A - - - intergenic_variant - - - - - - rs2776117 21:23191579 G - - - intergenic_variant - - - - - - rs9983429 21:23207412 G - - - intergenic_variant - - - - - - rs7279163 21:23207797 T - - - intergenic_variant - - - - - - rs9982251 21:23283039 G - - - intergenic_variant - - - - - - rs11909510 21:23506670 T - - - intergenic_variant - - - - - - rs9306056 21:23603516 G - - - intergenic_variant - - - - - - rs6518142 21:23639105 C - - - intergenic_variant - - - - - - rs1999306 21:23693502 A - - - intergenic_variant - - - - - - rs13047074 21:23743377 T - - - intergenic_variant - - - - - - rs2226811 21:23777619 G - - - intergenic_variant - - - - - - rs9979756 21:23859268 A - - - intergenic_variant - - - - - - rs243269 21:24236632 C - - - intergenic_variant - - - - - - rs58720278 21:24239317 T - - - intergenic_variant - - - - - - rs243272 21:24239738 T - - - intergenic_variant - - - - - - rs407402 21:24438339 C - - - intergenic_variant - - - - - - rs200692 21:24770618 T ENSESTG00000019888 ENSESTT00000049863 Transcript intron_variant - - - - - - rs200692 21:24770618 T ENSESTG00000019888 ENSESTT00000049852 Transcript intron_variant - - - - - - rs1699979 21:24817715 T - - - intergenic_variant - - - - - - rs1699991 21:24836176 T - - - intergenic_variant - - - - - - rs8131998 21:24855796 A - - - intergenic_variant - - - - - - rs9982132 21:24856027 A - - - intergenic_variant - - - - - - rs169478 21:25056382 T - - - intergenic_variant - - - - - - rs6516573 21:25100956 C - - - intergenic_variant - - - - - - rs423410 21:25205423 A - - - intergenic_variant - - - - - - rs2568510 21:25244781 C - - - intergenic_variant - - - - - - rs207475 21:25268288 T - - - intergenic_variant - - - - - - rs76902935 21:25268730 C - - - intergenic_variant - - - - - - rs2186432 21:25276025 T - - - intergenic_variant - - - - - - rs9977538 21:25333378 C - - - intergenic_variant - - - - - - rs4816925 21:25354037 G - - - intergenic_variant - - - - - - rs2018559 21:25378535 T - - - intergenic_variant - - - - - - rs1699625 21:25438514 T - - - intergenic_variant - - - - - - rs1617671 21:25438776 G - - - intergenic_variant - - - - - - rs1699710 21:25457128 G - - - intergenic_variant - - - - - - rs1783387 21:25526656 T - - - intergenic_variant - - - - - - rs8132449 21:25615099 A - - - intergenic_variant - - - - - - rs11909463 21:25625429 A - - - intergenic_variant - - - - - - rs75244939 21:25636726 A - - - intergenic_variant - - - - - - rs6516613 21:25654454 G - - - intergenic_variant - - - - - - rs2212008 21:25798104 A ENSESTG00000019310 ENSESTT00000048511 Transcript upstream_gene_variant - - - - - - DISTANCE=2950 rs2212008 21:25798104 A ENSESTG00000019310 ENSESTT00000048532 Transcript upstream_gene_variant - - - - - - DISTANCE=2961 rs8126911 21:25803217 A ENSESTG00000019310 ENSESTT00000048511 Transcript intron_variant - - - - - - rs8126911 21:25803217 A ENSESTG00000019310 ENSESTT00000048532 Transcript intron_variant - - - - - - rs7277842 21:25822127 T - - - intergenic_variant - - - - - - rs4816962 21:25832950 T - - - intergenic_variant - - - - - - rs2226673 21:26038119 A - - - intergenic_variant - - - - - - rs7280651 21:26089882 A - - - intergenic_variant - - - - - - rs987602 21:26131067 C - - - intergenic_variant - - - - - - rs9984373 21:26171576 A - - - intergenic_variant - - - - - - rs7276736 21:26171687 A - - - intergenic_variant - - - - - - rs8133580 21:26174283 T - ENSR00000612004 RegulatoryFeature regulatory_region_variant - - - - - - rs8133580 21:26174283 T - - - intergenic_variant - - - - - - rs1009928 21:26197584 C - - - intergenic_variant - - - - - - rs8128344 21:26217672 A 339622 NR_046198.3 Transcript intron_variant,nc_transcript_variant - - - - - - rs2026218 21:26225547 C 339622 NR_046198.3 Transcript intron_variant,nc_transcript_variant - - - - - - rs2211831 21:26353050 T 339622 NR_046198.3 Transcript intron_variant,nc_transcript_variant - - - - - - rs9980380 21:26413533 A 339622 NR_046198.3 Transcript intron_variant,nc_transcript_variant - - - - - - rs9974862 21:26446898 A - - - intergenic_variant - - - - - - rs8129441 21:26462169 A - - - intergenic_variant - - - - - - rs9305245 21:26502859 G ENSESTG00000019390 ENSESTT00000048709 Transcript intron_variant - - - - - - rs4817004 21:26504168 T ENSESTG00000019390 ENSESTT00000048709 Transcript intron_variant - - - - - - rs12627466 21:26567465 G - - - intergenic_variant - - - - - - rs8128240 21:26630039 C - - - intergenic_variant - - - - - - rs8131876 21:26630222 A - - - intergenic_variant - - - - - - rs4816253 21:26670311 A - - - intergenic_variant - - - - - - rs8130858 21:26714849 T - - - intergenic_variant - - - - - - rs4817014 21:26734301 C - - - intergenic_variant - - - - - - rs7276628 21:27023748 C 58494 NM_001270408.1 Transcript intron_variant - - - - - - rs7276628 21:27023748 C CCDS58788.1 CCDS58788.1 Transcript intron_variant - - - - - - rs7276628 21:27023748 C 58494 NM_021219.3 Transcript intron_variant - - - - - - rs7276628 21:27023748 C CCDS58787.1 CCDS58787.1 Transcript intron_variant - - - - - - rs7276628 21:27023748 C 58494 NR_072999.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7276628 21:27023748 C ENSESTG00000031547 ENSESTT00000079609 Transcript intron_variant - - - - - - rs7276628 21:27023748 C CCDS42911.1 CCDS42911.1 Transcript intron_variant - - - - - - rs7276628 21:27023748 C ENSESTG00000031547 ENSESTT00000079661 Transcript intron_variant - - - - - - rs7276628 21:27023748 C 58494 NM_001270407.1 Transcript intron_variant - - - - - - rs2065247 21:27123425 T 2551 NM_001197297.1 Transcript intron_variant - - - - - - rs2065247 21:27123425 T CCDS13575.1 CCDS13575.1 Transcript intron_variant - - - - - - rs2065247 21:27123425 T ENSESTG00000031613 ENSESTT00000079794 Transcript intron_variant - - - - - - rs2065247 21:27123425 T ENSESTG00000031613 ENSESTT00000079784 Transcript intron_variant - - - - - - rs2065247 21:27123425 T ENSESTG00000031613 ENSESTT00000079764 Transcript intron_variant - - - - - - rs2065247 21:27123425 T ENSESTG00000031613 ENSESTT00000079810 Transcript upstream_gene_variant - - - - - - DISTANCE=677 rs2065247 21:27123425 T 2551 NM_002040.3 Transcript intron_variant - - - - - - rs2154472 21:27143162 A 2551 NM_001197297.1 Transcript 3_prime_UTR_variant 3134 - - - - - rs2154472 21:27143162 A CCDS13575.1 CCDS13575.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1619 rs2154472 21:27143162 A 2551 NM_002040.3 Transcript 3_prime_UTR_variant 3571 - - - - - rs1700991 21:27260667 G 351 NM_201414.2 Transcript intron_variant - - - - - - rs1700991 21:27260667 G 351 NM_000484.3 Transcript intron_variant - - - - - - rs1700991 21:27260667 G ENSESTG00000031739 ENSESTT00000080252 Transcript downstream_gene_variant - - - - - - DISTANCE=3457 rs1700991 21:27260667 G CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G 351 NM_001204301.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G 351 NM_001136016.3 Transcript intron_variant - - - - - - rs1700991 21:27260667 G CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs1700991 21:27260667 G 351 NM_001136129.2 Transcript intron_variant - - - - - - rs1700991 21:27260667 G CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G 351 NM_201413.2 Transcript intron_variant - - - - - - rs1700991 21:27260667 G 351 NM_001136130.2 Transcript intron_variant - - - - - - rs1700991 21:27260667 G 351 NM_001136131.2 Transcript intron_variant - - - - - - rs1700991 21:27260667 G ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs1700991 21:27260667 G 351 NM_001204303.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs1700991 21:27260667 G CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G 351 NM_001204302.1 Transcript intron_variant - - - - - - rs1700991 21:27260667 G CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_201414.2 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_000484.3 Transcript intron_variant - - - - - - rs389250 21:27275753 T ENSESTG00000031739 ENSESTT00000080252 Transcript intron_variant - - - - - - rs389250 21:27275753 T CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_001204301.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_001136016.3 Transcript intron_variant - - - - - - rs389250 21:27275753 T CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_001136129.2 Transcript intron_variant - - - - - - rs389250 21:27275753 T CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_201413.2 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_001136130.2 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_001136131.2 Transcript intron_variant - - - - - - rs389250 21:27275753 T ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_001204303.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs389250 21:27275753 T CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T ENSESTG00000031739 ENSESTT00000080263 Transcript intron_variant - - - - - - rs389250 21:27275753 T 351 NM_001204302.1 Transcript intron_variant - - - - - - rs389250 21:27275753 T CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_201414.2 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_000484.3 Transcript intron_variant - - - - - - rs453180 21:27299803 C ENSESTG00000031739 ENSESTT00000080252 Transcript intron_variant - - - - - - rs453180 21:27299803 C CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_001204301.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_001136016.3 Transcript intron_variant - - - - - - rs453180 21:27299803 C CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_001136129.2 Transcript intron_variant - - - - - - rs453180 21:27299803 C CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_201413.2 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_001136130.2 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_001136131.2 Transcript intron_variant - - - - - - rs453180 21:27299803 C ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_001204303.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs453180 21:27299803 C CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C ENSESTG00000031739 ENSESTT00000080263 Transcript intron_variant - - - - - - rs453180 21:27299803 C 351 NM_001204302.1 Transcript intron_variant - - - - - - rs453180 21:27299803 C CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C - ENSR00000612142 RegulatoryFeature regulatory_region_variant - - - - - - rs214481 21:27302648 C 351 NM_201414.2 Transcript intron_variant - - - - - - rs214481 21:27302648 C 351 NM_000484.3 Transcript intron_variant - - - - - - rs214481 21:27302648 C ENSESTG00000031739 ENSESTT00000080252 Transcript intron_variant - - - - - - rs214481 21:27302648 C CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C 351 NM_001204301.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C 351 NM_001136016.3 Transcript intron_variant - - - - - - rs214481 21:27302648 C CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs214481 21:27302648 C 351 NM_001136129.2 Transcript intron_variant - - - - - - rs214481 21:27302648 C CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C 351 NM_201413.2 Transcript intron_variant - - - - - - rs214481 21:27302648 C 351 NM_001136130.2 Transcript intron_variant - - - - - - rs214481 21:27302648 C 351 NM_001136131.2 Transcript intron_variant - - - - - - rs214481 21:27302648 C ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs214481 21:27302648 C 351 NM_001204303.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs214481 21:27302648 C CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C ENSESTG00000031739 ENSESTT00000080263 Transcript intron_variant - - - - - - rs214481 21:27302648 C 351 NM_001204302.1 Transcript intron_variant - - - - - - rs214481 21:27302648 C CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_201414.2 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_000484.3 Transcript intron_variant - - - - - - rs1783021 21:27314373 A ENSESTG00000031739 ENSESTT00000080252 Transcript intron_variant - - - - - - rs1783021 21:27314373 A CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_001204301.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_001136016.3 Transcript intron_variant - - - - - - rs1783021 21:27314373 A CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_001136129.2 Transcript intron_variant - - - - - - rs1783021 21:27314373 A CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_201413.2 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_001136130.2 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_001136131.2 Transcript intron_variant - - - - - - rs1783021 21:27314373 A ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_001204303.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs1783021 21:27314373 A CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A ENSESTG00000031739 ENSESTT00000080263 Transcript intron_variant - - - - - - rs1783021 21:27314373 A 351 NM_001204302.1 Transcript intron_variant - - - - - - rs1783021 21:27314373 A CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T - ENSR00000612149 RegulatoryFeature regulatory_region_variant - - - - - - rs409215 21:27326065 T 351 NM_201414.2 Transcript intron_variant - - - - - - rs409215 21:27326065 T 351 NM_000484.3 Transcript intron_variant - - - - - - rs409215 21:27326065 T ENSESTG00000031739 ENSESTT00000080252 Transcript intron_variant - - - - - - rs409215 21:27326065 T CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T 351 NM_001204301.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T 351 NM_001136016.3 Transcript intron_variant - - - - - - rs409215 21:27326065 T CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs409215 21:27326065 T 351 NM_001136129.2 Transcript intron_variant - - - - - - rs409215 21:27326065 T CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T 351 NM_201413.2 Transcript intron_variant - - - - - - rs409215 21:27326065 T 351 NM_001136130.2 Transcript intron_variant - - - - - - rs409215 21:27326065 T 351 NM_001136131.2 Transcript intron_variant - - - - - - rs409215 21:27326065 T ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs409215 21:27326065 T 351 NM_001204303.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs409215 21:27326065 T CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T ENSESTG00000031739 ENSESTT00000080263 Transcript intron_variant - - - - - - rs409215 21:27326065 T 351 NM_001204302.1 Transcript intron_variant - - - - - - rs409215 21:27326065 T CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_201414.2 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_000484.3 Transcript intron_variant - - - - - - rs9982027 21:27350135 A CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_001204301.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_001136016.3 Transcript intron_variant - - - - - - rs9982027 21:27350135 A CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs9982027 21:27350135 A ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs9982027 21:27350135 A CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_001136129.2 Transcript intron_variant - - - - - - rs9982027 21:27350135 A ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs9982027 21:27350135 A CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_201413.2 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_001136130.2 Transcript intron_variant - - - - - - rs9982027 21:27350135 A ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_001136131.2 Transcript intron_variant - - - - - - rs9982027 21:27350135 A ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs9982027 21:27350135 A ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_001204303.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs9982027 21:27350135 A CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A 351 NM_001204302.1 Transcript intron_variant - - - - - - rs9982027 21:27350135 A CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_201414.2 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_000484.3 Transcript intron_variant - - - - - - rs1612963 21:27351273 A CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_001204301.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_001136016.3 Transcript intron_variant - - - - - - rs1612963 21:27351273 A CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs1612963 21:27351273 A ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs1612963 21:27351273 A CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_001136129.2 Transcript intron_variant - - - - - - rs1612963 21:27351273 A ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs1612963 21:27351273 A CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_201413.2 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_001136130.2 Transcript intron_variant - - - - - - rs1612963 21:27351273 A ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_001136131.2 Transcript intron_variant - - - - - - rs1612963 21:27351273 A ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs1612963 21:27351273 A ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_001204303.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs1612963 21:27351273 A CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A 351 NM_001204302.1 Transcript intron_variant - - - - - - rs1612963 21:27351273 A CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_201414.2 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_000484.3 Transcript intron_variant - - - - - - rs7276426 21:27363183 C CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_001204301.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_001136016.3 Transcript intron_variant - - - - - - rs7276426 21:27363183 C CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs7276426 21:27363183 C ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs7276426 21:27363183 C CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_001136129.2 Transcript intron_variant - - - - - - rs7276426 21:27363183 C ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs7276426 21:27363183 C CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_201413.2 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_001136130.2 Transcript intron_variant - - - - - - rs7276426 21:27363183 C ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_001136131.2 Transcript intron_variant - - - - - - rs7276426 21:27363183 C ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs7276426 21:27363183 C ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_001204303.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs7276426 21:27363183 C CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C 351 NM_001204302.1 Transcript intron_variant - - - - - - rs7276426 21:27363183 C CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_201414.2 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_000484.3 Transcript intron_variant - - - - - - rs7276731 21:27363348 C CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_001204301.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_001136016.3 Transcript intron_variant - - - - - - rs7276731 21:27363348 C CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs7276731 21:27363348 C ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs7276731 21:27363348 C CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_001136129.2 Transcript intron_variant - - - - - - rs7276731 21:27363348 C ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs7276731 21:27363348 C CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_201413.2 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_001136130.2 Transcript intron_variant - - - - - - rs7276731 21:27363348 C ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_001136131.2 Transcript intron_variant - - - - - - rs7276731 21:27363348 C ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs7276731 21:27363348 C ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_001204303.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs7276731 21:27363348 C CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C 351 NM_001204302.1 Transcript intron_variant - - - - - - rs7276731 21:27363348 C CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_201414.2 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_000484.3 Transcript intron_variant - - - - - - rs2051504 21:27369481 T CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_001204301.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_001136016.3 Transcript intron_variant - - - - - - rs2051504 21:27369481 T CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs2051504 21:27369481 T ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs2051504 21:27369481 T CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_001136129.2 Transcript intron_variant - - - - - - rs2051504 21:27369481 T ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs2051504 21:27369481 T CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_201413.2 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_001136130.2 Transcript intron_variant - - - - - - rs2051504 21:27369481 T ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_001136131.2 Transcript intron_variant - - - - - - rs2051504 21:27369481 T ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs2051504 21:27369481 T ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_001204303.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs2051504 21:27369481 T CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T 351 NM_001204302.1 Transcript intron_variant - - - - - - rs2051504 21:27369481 T CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G - ENSR00000612160 RegulatoryFeature regulatory_region_variant - - - - - - rs2154480 21:27370674 G 351 NM_201414.2 Transcript intron_variant - - - - - - rs2154480 21:27370674 G 351 NM_000484.3 Transcript intron_variant - - - - - - rs2154480 21:27370674 G CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G 351 NM_001204301.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs2154480 21:27370674 G 351 NM_001136016.3 Transcript intron_variant - - - - - - rs2154480 21:27370674 G CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs2154480 21:27370674 G ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs2154480 21:27370674 G CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs2154480 21:27370674 G 351 NM_001136129.2 Transcript intron_variant - - - - - - rs2154480 21:27370674 G ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs2154480 21:27370674 G CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G 351 NM_201413.2 Transcript intron_variant - - - - - - rs2154480 21:27370674 G 351 NM_001136130.2 Transcript intron_variant - - - - - - rs2154480 21:27370674 G ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs2154480 21:27370674 G 351 NM_001136131.2 Transcript intron_variant - - - - - - rs2154480 21:27370674 G ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs2154480 21:27370674 G ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs2154480 21:27370674 G 351 NM_001204303.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs2154480 21:27370674 G CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G 351 NM_001204302.1 Transcript intron_variant - - - - - - rs2154480 21:27370674 G CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_201414.2 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_000484.3 Transcript intron_variant - - - - - - rs1023374 21:27372818 T CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_001204301.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_001136016.3 Transcript intron_variant - - - - - - rs1023374 21:27372818 T CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs1023374 21:27372818 T ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs1023374 21:27372818 T CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_001136129.2 Transcript intron_variant - - - - - - rs1023374 21:27372818 T ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs1023374 21:27372818 T CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_201413.2 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_001136130.2 Transcript intron_variant - - - - - - rs1023374 21:27372818 T ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_001136131.2 Transcript intron_variant - - - - - - rs1023374 21:27372818 T ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs1023374 21:27372818 T ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_001204303.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs1023374 21:27372818 T CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T 351 NM_001204302.1 Transcript intron_variant - - - - - - rs1023374 21:27372818 T CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_201414.2 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_000484.3 Transcript intron_variant - - - - - - rs1023375 21:27372825 T CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_001204301.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_001136016.3 Transcript intron_variant - - - - - - rs1023375 21:27372825 T CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs1023375 21:27372825 T ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs1023375 21:27372825 T CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_001136129.2 Transcript intron_variant - - - - - - rs1023375 21:27372825 T ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs1023375 21:27372825 T CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_201413.2 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_001136130.2 Transcript intron_variant - - - - - - rs1023375 21:27372825 T ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_001136131.2 Transcript intron_variant - - - - - - rs1023375 21:27372825 T ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs1023375 21:27372825 T ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_001204303.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs1023375 21:27372825 T CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T 351 NM_001204302.1 Transcript intron_variant - - - - - - rs1023375 21:27372825 T CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_201414.2 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_000484.3 Transcript intron_variant - - - - - - rs1023376 21:27373118 T CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_001204301.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_001136016.3 Transcript intron_variant - - - - - - rs1023376 21:27373118 T CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs1023376 21:27373118 T ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs1023376 21:27373118 T CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_001136129.2 Transcript intron_variant - - - - - - rs1023376 21:27373118 T ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs1023376 21:27373118 T CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_201413.2 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_001136130.2 Transcript intron_variant - - - - - - rs1023376 21:27373118 T ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_001136131.2 Transcript intron_variant - - - - - - rs1023376 21:27373118 T ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs1023376 21:27373118 T ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_001204303.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs1023376 21:27373118 T CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T 351 NM_001204302.1 Transcript intron_variant - - - - - - rs1023376 21:27373118 T CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_201414.2 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_000484.3 Transcript intron_variant - - - - - - rs9305277 21:27376915 T CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_001204301.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_001136016.3 Transcript intron_variant - - - - - - rs9305277 21:27376915 T CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs9305277 21:27376915 T ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs9305277 21:27376915 T CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_001136129.2 Transcript intron_variant - - - - - - rs9305277 21:27376915 T ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs9305277 21:27376915 T CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_201413.2 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_001136130.2 Transcript intron_variant - - - - - - rs9305277 21:27376915 T ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_001136131.2 Transcript intron_variant - - - - - - rs9305277 21:27376915 T ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs9305277 21:27376915 T ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_001204303.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs9305277 21:27376915 T CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T 351 NM_001204302.1 Transcript intron_variant - - - - - - rs9305277 21:27376915 T CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T - ENSR00001565827 RegulatoryFeature regulatory_region_variant - - - - - - rs986464 21:27380780 T 351 NM_201414.2 Transcript intron_variant - - - - - - rs986464 21:27380780 T 351 NM_000484.3 Transcript intron_variant - - - - - - rs986464 21:27380780 T CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T 351 NM_001204301.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs986464 21:27380780 T 351 NM_001136016.3 Transcript intron_variant - - - - - - rs986464 21:27380780 T CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs986464 21:27380780 T ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs986464 21:27380780 T CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs986464 21:27380780 T 351 NM_001136129.2 Transcript intron_variant - - - - - - rs986464 21:27380780 T ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs986464 21:27380780 T CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T 351 NM_201413.2 Transcript intron_variant - - - - - - rs986464 21:27380780 T 351 NM_001136130.2 Transcript intron_variant - - - - - - rs986464 21:27380780 T ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs986464 21:27380780 T 351 NM_001136131.2 Transcript intron_variant - - - - - - rs986464 21:27380780 T ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs986464 21:27380780 T ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs986464 21:27380780 T 351 NM_001204303.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs986464 21:27380780 T CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T 351 NM_001204302.1 Transcript intron_variant - - - - - - rs986464 21:27380780 T CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_201414.2 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_000484.3 Transcript intron_variant - - - - - - rs2409166 21:27382417 G CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_001204301.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_001136016.3 Transcript intron_variant - - - - - - rs2409166 21:27382417 G CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs2409166 21:27382417 G ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs2409166 21:27382417 G CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_001136129.2 Transcript intron_variant - - - - - - rs2409166 21:27382417 G ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs2409166 21:27382417 G CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_201413.2 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_001136130.2 Transcript intron_variant - - - - - - rs2409166 21:27382417 G ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_001136131.2 Transcript intron_variant - - - - - - rs2409166 21:27382417 G ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs2409166 21:27382417 G ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_001204303.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs2409166 21:27382417 G CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G 351 NM_001204302.1 Transcript intron_variant - - - - - - rs2409166 21:27382417 G CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_201414.2 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_000484.3 Transcript intron_variant - - - - - - rs9305278 21:27388161 C CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_001204301.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_001136016.3 Transcript intron_variant - - - - - - rs9305278 21:27388161 C CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs9305278 21:27388161 C ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs9305278 21:27388161 C CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_001136129.2 Transcript intron_variant - - - - - - rs9305278 21:27388161 C ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs9305278 21:27388161 C CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_201413.2 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_001136130.2 Transcript intron_variant - - - - - - rs9305278 21:27388161 C ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_001136131.2 Transcript intron_variant - - - - - - rs9305278 21:27388161 C ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs9305278 21:27388161 C ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_001204303.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs9305278 21:27388161 C CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C 351 NM_001204302.1 Transcript intron_variant - - - - - - rs9305278 21:27388161 C CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_201414.2 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_000484.3 Transcript intron_variant - - - - - - rs928903 21:27390319 G CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_001204301.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_001136016.3 Transcript intron_variant - - - - - - rs928903 21:27390319 G CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G ENSESTG00000031657 ENSESTT00000080083 Transcript intron_variant - - - - - - rs928903 21:27390319 G ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs928903 21:27390319 G CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_001136129.2 Transcript intron_variant - - - - - - rs928903 21:27390319 G ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs928903 21:27390319 G CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_201413.2 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_001136130.2 Transcript intron_variant - - - - - - rs928903 21:27390319 G ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_001136131.2 Transcript intron_variant - - - - - - rs928903 21:27390319 G ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs928903 21:27390319 G ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_001204303.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs928903 21:27390319 G CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G 351 NM_001204302.1 Transcript intron_variant - - - - - - rs928903 21:27390319 G CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_201414.2 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_000484.3 Transcript intron_variant - - - - - - rs4817084 21:27436172 A CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_001204301.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A ENSESTG00000031657 ENSESTT00000080068 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_001136016.3 Transcript intron_variant - - - - - - rs4817084 21:27436172 A CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs4817084 21:27436172 A CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_001136129.2 Transcript intron_variant - - - - - - rs4817084 21:27436172 A ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs4817084 21:27436172 A CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_201413.2 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_001136130.2 Transcript intron_variant - - - - - - rs4817084 21:27436172 A ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_001136131.2 Transcript intron_variant - - - - - - rs4817084 21:27436172 A ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs4817084 21:27436172 A ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_001204303.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs4817084 21:27436172 A CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A 351 NM_001204302.1 Transcript intron_variant - - - - - - rs4817084 21:27436172 A CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_201414.2 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_000484.3 Transcript intron_variant - - - - - - rs4817088 21:27472526 G CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_001204301.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_001136016.3 Transcript intron_variant - - - - - - rs4817088 21:27472526 G CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs4817088 21:27472526 G CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_001136129.2 Transcript intron_variant - - - - - - rs4817088 21:27472526 G ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs4817088 21:27472526 G CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_201413.2 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_001136130.2 Transcript intron_variant - - - - - - rs4817088 21:27472526 G ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_001136131.2 Transcript intron_variant - - - - - - rs4817088 21:27472526 G ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs4817088 21:27472526 G ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_001204303.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs4817088 21:27472526 G CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G 351 NM_001204302.1 Transcript intron_variant - - - - - - rs4817088 21:27472526 G CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_201414.2 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_000484.3 Transcript intron_variant - - - - - - rs4817089 21:27476925 A CCDS13577.1 CCDS13577.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A CCDS56212.1 CCDS56212.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_001204301.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_001136016.3 Transcript intron_variant - - - - - - rs4817089 21:27476925 A CCDS46638.1 CCDS46638.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A CCDS56211.1 CCDS56211.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A ENSESTG00000031657 ENSESTT00000080048 Transcript intron_variant - - - - - - rs4817089 21:27476925 A CCDS46639.1 CCDS46639.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A ENSESTG00000031657 ENSESTT00000080033 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_001136129.2 Transcript intron_variant - - - - - - rs4817089 21:27476925 A ENSESTG00000031657 ENSESTT00000080035 Transcript intron_variant - - - - - - rs4817089 21:27476925 A CCDS33523.1 CCDS33523.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_201413.2 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_001136130.2 Transcript intron_variant - - - - - - rs4817089 21:27476925 A ENSESTG00000031657 ENSESTT00000079990 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_001136131.2 Transcript intron_variant - - - - - - rs4817089 21:27476925 A ENSESTG00000031657 ENSESTT00000080028 Transcript intron_variant - - - - - - rs4817089 21:27476925 A ENSESTG00000031657 ENSESTT00000080029 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_001204303.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A ENSESTG00000031657 ENSESTT00000079896 Transcript intron_variant - - - - - - rs4817089 21:27476925 A CCDS56213.1 CCDS56213.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A 351 NM_001204302.1 Transcript intron_variant - - - - - - rs4817089 21:27476925 A CCDS13576.1 CCDS13576.1 Transcript intron_variant - - - - - - rs467714 21:27594136 T - - - intergenic_variant - - - - - - rs219713 21:27751397 A - - - intergenic_variant - - - - - - rs233600 21:28328692 G - ENSR00001565912 RegulatoryFeature regulatory_region_variant - - - - - - rs233600 21:28328692 G ENSESTG00000000822 ENSESTT00000001989 Transcript intron_variant - - - - - - rs233600 21:28328692 G 100616243 NR_039916.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2330 rs233600 21:28328692 G 11096 NM_007038.3 Transcript intron_variant - - - - - - rs233600 21:28328692 G CCDS13579.1 CCDS13579.1 Transcript intron_variant - - - - - - rs417431 21:28525397 A - ENSR00001565929 RegulatoryFeature regulatory_region_variant - - - - - - rs417431 21:28525397 A - - - intergenic_variant - - - - - - rs239600 21:28730852 T ENSESTG00000008342 ENSESTT00000021068 Transcript intron_variant - - - - - - rs239600 21:28730852 T ENSESTG00000008344 ENSESTT00000021081 Transcript intron_variant - - - - - - rs9977367 21:29461327 T - - - intergenic_variant - - - - - - rs9305362 21:29576052 G - - - intergenic_variant - - - - - - rs2982542 21:29719170 C - - - intergenic_variant - - - - - - rs1738102 21:29737010 C - - - intergenic_variant - - - - - - rs1738156 21:29758088 C - - - intergenic_variant - - - - - - rs992272 21:29759298 G - - - intergenic_variant - - - - - - rs992273 21:29759373 G - - - intergenic_variant - - - - - - rs3886326 21:29760449 T - - - intergenic_variant - - - - - - rs4266097 21:29768490 C - - - intergenic_variant - - - - - - rs4144591 21:29770216 G - - - intergenic_variant - - - - - - rs4817231 21:29776769 G - - - intergenic_variant - - - - - - rs2205329 21:29796213 C - - - intergenic_variant - - - - - - rs428728 21:29797734 G - - - intergenic_variant - - - - - - rs435156 21:29798738 G - - - intergenic_variant - - - - - - rs447436 21:29798839 G - - - intergenic_variant - - - - - - rs2736403 21:29799585 C - - - intergenic_variant - - - - - - rs2737070 21:29799656 C - ENSR00001566012 RegulatoryFeature regulatory_region_variant - - - - - - rs2737070 21:29799656 C - - - intergenic_variant - - - - - - rs385705 21:29802903 G - - - intergenic_variant - - - - - - rs371226 21:29803219 G - - - intergenic_variant - - - - - - rs59514 21:29803518 G - ENSR00001051103 RegulatoryFeature regulatory_region_variant - - - - - - rs59514 21:29803518 G - - - intergenic_variant - - - - - - rs2736400 21:29805311 C - ENSR00000612457 RegulatoryFeature regulatory_region_variant - - - - - - rs2736400 21:29805311 C - - - intergenic_variant - - - - - - rs2736399 21:29807378 C - - - intergenic_variant - - - - - - rs2223094 21:29807591 C - - - intergenic_variant - - - - - - rs2736396 21:29807719 C - - - intergenic_variant - - - - - - rs433743 21:29808041 G - - - intergenic_variant - - - - - - rs2776162 21:29809609 C - - - intergenic_variant - - - - - - rs2776163 21:29809776 C - - - intergenic_variant - - - - - - rs2737068 21:29813441 G - - - intergenic_variant - - - - - - rs364943 21:29815510 G - - - intergenic_variant - - - - - - rs2776166 21:29820172 C - ENSR00001566018 RegulatoryFeature regulatory_region_variant - - - - - - rs2776166 21:29820172 C - - - intergenic_variant - - - - - - rs406293 21:29825564 G - - - intergenic_variant - - - - - - rs2776169 21:29827042 C - - - intergenic_variant - - - - - - rs383712 21:29829430 G - - - intergenic_variant - - - - - - rs59429 21:29829705 G - - - intergenic_variant - - - - - - rs403762 21:29831252 G - - - intergenic_variant - - - - - - rs413442 21:29832565 G - - - intergenic_variant - - - - - - rs434289 21:29835139 G - - - intergenic_variant - - - - - - rs4544527 21:29836487 A - - - intergenic_variant - - - - - - rs2142319 21:29838244 G - - - intergenic_variant - - - - - - rs4626006 21:29838438 G - - - intergenic_variant - - - - - - rs9979783 21:29839100 C - - - intergenic_variant - - - - - - rs4816318 21:29846647 G - - - intergenic_variant - - - - - - rs6516845 21:29847182 G - - - intergenic_variant - - - - - - rs8129748 21:29855072 G - - - intergenic_variant - - - - - - rs2210249 21:29911122 G 118421 NR_026552.1 Transcript upstream_gene_variant - - - - - - DISTANCE=518 rs2210249 21:29911122 G ENSESTG00000009181 ENSESTT00000023008 Transcript upstream_gene_variant - - - - - - DISTANCE=791 rs2210249 21:29911122 G 118421 NR_026553.1 Transcript upstream_gene_variant - - - - - - DISTANCE=518 rs2210250 21:29911125 G 118421 NR_026552.1 Transcript upstream_gene_variant - - - - - - DISTANCE=515 rs2210250 21:29911125 G ENSESTG00000009181 ENSESTT00000023008 Transcript upstream_gene_variant - - - - - - DISTANCE=788 rs2210250 21:29911125 G 118421 NR_026553.1 Transcript upstream_gene_variant - - - - - - DISTANCE=515 rs2205369 21:29934861 C - - - intergenic_variant - - - - - - rs2205247 21:29959599 G - - - intergenic_variant - - - - - - rs12152020 21:29984773 C - - - intergenic_variant - - - - - - rs1153269 21:30013372 T - - - intergenic_variant - - - - - - rs9977438 21:30028194 T - - - intergenic_variant - - - - - - rs8134938 21:30028471 G - - - intergenic_variant - - - - - - rs4239789 21:30035425 A - - - intergenic_variant - - - - - - rs4816320 21:30057521 C - - - intergenic_variant - - - - - - rs2205422 21:30058334 C - - - intergenic_variant - - - - - - rs8133844 21:30059391 G - - - intergenic_variant - - - - - - rs760400 21:30059993 G - ENSR00000612484 RegulatoryFeature regulatory_region_variant - - - - - - rs760400 21:30059993 G - - - intergenic_variant - - - - - - rs7275256 21:30063421 T - - - intergenic_variant - - - - - - rs11700475 21:30083190 C - - - intergenic_variant - - - - - - rs4816330 21:30104103 A - - - intergenic_variant - - - - - - rs962996 21:30107448 G - ENSR00000612490 RegulatoryFeature regulatory_region_variant - - - - - - rs962996 21:30107448 G - - - intergenic_variant - - - - - - rs767109 21:30108151 A - - - intergenic_variant - - - - - - rs74964454 21:30109255 C - - - intergenic_variant - - - - - - rs1118642 21:30180912 G - - - intergenic_variant - - - - - - rs2705655 21:30213129 A - - - intergenic_variant - - - - - - rs2705682 21:30236368 G - - - intergenic_variant - - - - - - rs2705693 21:30240675 A 29104 NR_047510.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3838 rs1571679 21:30242509 G 29104 NR_047510.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2004 rs2183566 21:30242687 T 29104 NR_047510.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1826 rs1554989 21:30243123 A 29104 NR_047510.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1390 rs2738955 21:30244213 T 29104 NM_182749.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4173 rs2738955 21:30244213 T 29104 NM_013240.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4173 rs2738955 21:30244213 T 29104 NR_047510.1 Transcript downstream_gene_variant - - - - - - DISTANCE=300 rs2738955 21:30244213 T CCDS33525.1 CCDS33525.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4494 rs2738955 21:30244213 T ENSESTG00000009315 ENSESTT00000023359 Transcript downstream_gene_variant - - - - - - DISTANCE=4501 rs2738955 21:30244213 T ENSESTG00000009315 ENSESTT00000023368 Transcript downstream_gene_variant - - - - - - DISTANCE=4423 rs2738955 21:30244213 T CCDS33526.1 CCDS33526.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4494 rs2776199 21:30244666 C - ENSR00001566054 RegulatoryFeature regulatory_region_variant - - - - - - rs2776199 21:30244666 C 29104 NM_182749.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3720 rs2776199 21:30244666 C 29104 NM_013240.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3720 rs2776199 21:30244666 C 29104 NR_047510.1 Transcript non_coding_exon_variant,nc_transcript_variant 1142 - - - - - rs2776199 21:30244666 C CCDS33525.1 CCDS33525.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4041 rs2776199 21:30244666 C ENSESTG00000009315 ENSESTT00000023359 Transcript downstream_gene_variant - - - - - - DISTANCE=4048 rs2776199 21:30244666 C ENSESTG00000009315 ENSESTT00000023368 Transcript downstream_gene_variant - - - - - - DISTANCE=3970 rs2776199 21:30244666 C CCDS33526.1 CCDS33526.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4041 rs8134912 21:30244816 C 29104 NM_182749.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3570 rs8134912 21:30244816 C 29104 NM_013240.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3570 rs8134912 21:30244816 C 29104 NR_047510.1 Transcript non_coding_exon_variant,nc_transcript_variant 992 - - - - - rs8134912 21:30244816 C CCDS33525.1 CCDS33525.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3891 rs8134912 21:30244816 C ENSESTG00000009315 ENSESTT00000023359 Transcript downstream_gene_variant - - - - - - DISTANCE=3898 rs8134912 21:30244816 C ENSESTG00000009315 ENSESTT00000023368 Transcript downstream_gene_variant - - - - - - DISTANCE=3820 rs8134912 21:30244816 C CCDS33526.1 CCDS33526.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3891 rs2776202 21:30244895 C 29104 NM_182749.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3491 rs2776202 21:30244895 C 29104 NM_013240.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3491 rs2776202 21:30244895 C 29104 NR_047510.1 Transcript non_coding_exon_variant,nc_transcript_variant 913 - - - - - rs2776202 21:30244895 C CCDS33525.1 CCDS33525.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3812 rs2776202 21:30244895 C ENSESTG00000009315 ENSESTT00000023359 Transcript downstream_gene_variant - - - - - - DISTANCE=3819 rs2776202 21:30244895 C ENSESTG00000009315 ENSESTT00000023368 Transcript downstream_gene_variant - - - - - - DISTANCE=3741 rs2776202 21:30244895 C CCDS33526.1 CCDS33526.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3812 rs2776204 21:30245466 C 29104 NM_182749.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2920 rs2776204 21:30245466 C 29104 NM_013240.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2920 rs2776204 21:30245466 C 29104 NR_047510.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2776204 21:30245466 C CCDS33525.1 CCDS33525.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3241 rs2776204 21:30245466 C ENSESTG00000009315 ENSESTT00000023359 Transcript downstream_gene_variant - - - - - - DISTANCE=3248 rs2776204 21:30245466 C ENSESTG00000009315 ENSESTT00000023368 Transcript downstream_gene_variant - - - - - - DISTANCE=3170 rs2776204 21:30245466 C CCDS33526.1 CCDS33526.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3241 rs2738959 21:30250327 A 29104 NM_182749.3 Transcript intron_variant - - - - - - rs2738959 21:30250327 A 29104 NM_013240.4 Transcript intron_variant - - - - - - rs2738959 21:30250327 A 29104 NR_047510.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2738959 21:30250327 A CCDS33525.1 CCDS33525.1 Transcript intron_variant - - - - - - rs2738959 21:30250327 A ENSESTG00000009315 ENSESTT00000023359 Transcript intron_variant - - - - - - rs2738959 21:30250327 A ENSESTG00000009315 ENSESTT00000023368 Transcript intron_variant - - - - - - rs2738959 21:30250327 A CCDS33526.1 CCDS33526.1 Transcript intron_variant - - - - - - rs2738960 21:30250382 C 29104 NM_182749.3 Transcript intron_variant - - - - - - rs2738960 21:30250382 C 29104 NM_013240.4 Transcript intron_variant - - - - - - rs2738960 21:30250382 C 29104 NR_047510.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2738960 21:30250382 C CCDS33525.1 CCDS33525.1 Transcript intron_variant - - - - - - rs2738960 21:30250382 C ENSESTG00000009315 ENSESTT00000023359 Transcript intron_variant - - - - - - rs2738960 21:30250382 C ENSESTG00000009315 ENSESTT00000023368 Transcript intron_variant - - - - - - rs2738960 21:30250382 C CCDS33526.1 CCDS33526.1 Transcript intron_variant - - - - - - rs2205448 21:30250812 C 29104 NM_182749.3 Transcript intron_variant - - - - - - rs2205448 21:30250812 C 29104 NM_013240.4 Transcript intron_variant - - - - - - rs2205448 21:30250812 C 29104 NR_047510.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2205448 21:30250812 C CCDS33525.1 CCDS33525.1 Transcript intron_variant - - - - - - rs2205448 21:30250812 C ENSESTG00000009315 ENSESTT00000023359 Transcript intron_variant - - - - - - rs2205448 21:30250812 C ENSESTG00000009315 ENSESTT00000023368 Transcript intron_variant - - - - - - rs2205448 21:30250812 C CCDS33526.1 CCDS33526.1 Transcript intron_variant - - - - - - rs1997607 21:30257568 C - ENSR00000185543 RegulatoryFeature regulatory_region_variant - - - - - - rs1997607 21:30257568 C 29104 NM_182749.3 Transcript missense_variant 128 100 34 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs1997607 21:30257568 C 29104 NM_013240.4 Transcript missense_variant 128 100 34 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs1997607 21:30257568 C 29104 NR_047510.1 Transcript non_coding_exon_variant,nc_transcript_variant 128 - - - - - rs1997607 21:30257568 C CCDS33525.1 CCDS33525.1 Transcript missense_variant 100 100 34 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs1997607 21:30257568 C ENSESTG00000009315 ENSESTT00000023359 Transcript missense_variant 120 100 34 N/D Aac/Gac - rs1997607 21:30257568 C ENSESTG00000009315 ENSESTT00000023368 Transcript 5_prime_UTR_variant 81 - - - - - rs1997607 21:30257568 C CCDS33526.1 CCDS33526.1 Transcript missense_variant 100 100 34 N/D Aac/Gac - PolyPhen=benign;SIFT=tolerated rs2178966 21:30275060 G - - - intergenic_variant - - - - - - rs2853829 21:30451922 A - ENSR00000612531 RegulatoryFeature regulatory_region_variant - - - - - - rs2853829 21:30451922 A 56911 NM_020152.2 Transcript upstream_gene_variant - - - - - - DISTANCE=951 rs2853829 21:30451922 A ENSESTG00000007466 ENSESTT00000018806 Transcript intron_variant - - - - - - rs11700432 21:30498781 T ENSESTG00000007478 ENSESTT00000018891 Transcript upstream_gene_variant - - - - - - DISTANCE=4797 rs11700432 21:30498781 T ENSESTG00000007478 ENSESTT00000018878 Transcript upstream_gene_variant - - - - - - DISTANCE=4219 rs11700432 21:30498781 T CCDS13584.1 CCDS13584.1 Transcript intron_variant - - - - - - rs11700432 21:30498781 T ENSESTG00000007478 ENSESTT00000018853 Transcript intron_variant - - - - - - rs11700432 21:30498781 T ENSESTG00000007478 ENSESTT00000018886 Transcript upstream_gene_variant - - - - - - DISTANCE=4754 rs11700432 21:30498781 T 56911 NM_020152.2 Transcript intron_variant - - - - - - rs1467749 21:30501056 C ENSESTG00000007478 ENSESTT00000018891 Transcript upstream_gene_variant - - - - - - DISTANCE=2522 rs1467749 21:30501056 C ENSESTG00000007478 ENSESTT00000018878 Transcript upstream_gene_variant - - - - - - DISTANCE=1944 rs1467749 21:30501056 C CCDS13584.1 CCDS13584.1 Transcript intron_variant - - - - - - rs1467749 21:30501056 C ENSESTG00000007478 ENSESTT00000018853 Transcript intron_variant - - - - - - rs1467749 21:30501056 C ENSESTG00000007478 ENSESTT00000018886 Transcript upstream_gene_variant - - - - - - DISTANCE=2479 rs1467749 21:30501056 C 56911 NM_020152.2 Transcript intron_variant - - - - - - rs1034124 21:30517644 C - ENSR00000612545 RegulatoryFeature regulatory_region_variant - - - - - - rs1034124 21:30517644 C ENSESTG00000007478 ENSESTT00000018891 Transcript intron_variant - - - - - - rs1034124 21:30517644 C ENSESTG00000007478 ENSESTT00000018878 Transcript intron_variant - - - - - - rs1034124 21:30517644 C CCDS13584.1 CCDS13584.1 Transcript intron_variant - - - - - - rs1034124 21:30517644 C ENSESTG00000007478 ENSESTT00000018853 Transcript intron_variant - - - - - - rs1034124 21:30517644 C ENSESTG00000007478 ENSESTT00000018886 Transcript intron_variant - - - - - - rs1034124 21:30517644 C ENSESTG00000007478 ENSESTT00000018901 Transcript upstream_gene_variant - - - - - - DISTANCE=241 rs1034124 21:30517644 C 56911 NM_020152.2 Transcript intron_variant - - - - - - rs1153273 21:30657371 G 193629 NR_027072.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs1153273 21:30657371 G ENSESTG00000007510 ENSESTT00000018948 Transcript intron_variant - - - - - - rs1153273 21:30657371 G ENSESTG00000007510 ENSESTT00000018951 Transcript intron_variant - - - - - - rs1153275 21:30660302 C 193629 NR_027072.2 Transcript splice_region_variant,intron_variant,nc_transcript_variant - - - - - - rs1153275 21:30660302 C ENSESTG00000007510 ENSESTT00000018948 Transcript splice_region_variant,intron_variant - - - - - - rs1153275 21:30660302 C ENSESTG00000007510 ENSESTT00000018951 Transcript splice_region_variant,intron_variant - - - - - - rs1153283 21:30682931 T - ENSR00000612593 RegulatoryFeature regulatory_region_variant - - - - - - rs1153283 21:30682931 T 571 NR_027655.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1153283 21:30682931 T 571 NM_001186.2 Transcript intron_variant - - - - - - rs1153283 21:30682931 T ENSESTG00000007510 ENSESTT00000018948 Transcript intron_variant - - - - - - rs1153283 21:30682931 T 571 NM_206866.1 Transcript intron_variant - - - - - - rs1153283 21:30682931 T ENSESTG00000007510 ENSESTT00000018973 Transcript intron_variant - - - - - - rs1153283 21:30682931 T ENSESTG00000007510 ENSESTT00000018965 Transcript intron_variant - - - - - - rs1153283 21:30682931 T ENSESTG00000007510 ENSESTT00000018954 Transcript intron_variant - - - - - - rs8128528 21:30772716 G - - - intergenic_variant - - - - - - rs2226334 21:30779882 A - - - intergenic_variant - - - - - - rs7276796 21:30780329 T - - - intergenic_variant - - - - - - rs2051379 21:30942225 T 2897 NM_000830.3 Transcript intron_variant - - - - - - rs2051379 21:30942225 T CCDS33530.1 CCDS33530.1 Transcript intron_variant - - - - - - rs2051379 21:30942225 T 2897 NM_175611.2 Transcript intron_variant - - - - - - rs2051379 21:30942225 T CCDS42913.1 CCDS42913.1 Transcript intron_variant - - - - - - rs377064 21:31176730 A 2897 NM_000830.3 Transcript intron_variant - - - - - - rs377064 21:31176730 A CCDS33530.1 CCDS33530.1 Transcript intron_variant - - - - - - rs377064 21:31176730 A 2897 NM_175611.2 Transcript intron_variant - - - - - - rs377064 21:31176730 A CCDS42913.1 CCDS42913.1 Transcript intron_variant - - - - - - rs461637 21:31217220 T 2897 NM_000830.3 Transcript intron_variant - - - - - - rs461637 21:31217220 T CCDS33530.1 CCDS33530.1 Transcript intron_variant - - - - - - rs461637 21:31217220 T 2897 NM_175611.2 Transcript intron_variant - - - - - - rs461637 21:31217220 T CCDS42913.1 CCDS42913.1 Transcript intron_variant - - - - - - rs386657 21:31226710 C 2897 NM_000830.3 Transcript intron_variant - - - - - - rs386657 21:31226710 C CCDS33530.1 CCDS33530.1 Transcript intron_variant - - - - - - rs386657 21:31226710 C 2897 NM_175611.2 Transcript intron_variant - - - - - - rs386657 21:31226710 C CCDS42913.1 CCDS42913.1 Transcript intron_variant - - - - - - rs459729 21:31294453 T 2897 NM_000830.3 Transcript intron_variant - - - - - - rs459729 21:31294453 T CCDS33530.1 CCDS33530.1 Transcript intron_variant - - - - - - rs459729 21:31294453 T 2897 NM_175611.2 Transcript intron_variant - - - - - - rs459729 21:31294453 T CCDS42913.1 CCDS42913.1 Transcript intron_variant - - - - - - rs455431 21:31298678 T 2897 NM_000830.3 Transcript intron_variant - - - - - - rs455431 21:31298678 T CCDS33530.1 CCDS33530.1 Transcript intron_variant - - - - - - rs455431 21:31298678 T 2897 NM_175611.2 Transcript intron_variant - - - - - - rs455431 21:31298678 T CCDS42913.1 CCDS42913.1 Transcript intron_variant - - - - - - rs456891 21:31320549 C - - - intergenic_variant - - - - - - rs456693 21:31355617 C - - - intergenic_variant - - - - - - rs478077 21:31531894 T ENSESTG00000010126 ENSESTT00000025334 Transcript intron_variant - - - - - - rs495158 21:31544655 T - - - intergenic_variant - - - - - - rs1557291 21:31655212 C CCDS42915.1 CCDS42915.1 Transcript synonymous_variant 39 39 13 G ggT/ggG - rs1557291 21:31655212 C 643803 NM_001085455.1 Transcript synonymous_variant 65 39 13 G ggT/ggG - rs198874 21:31965914 G 100288287 NM_001164434.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3198 rs198874 21:31965914 G CCDS46641.1 CCDS46641.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3221 rs198874 21:31965914 G 337968 NM_181605.3 Transcript downstream_gene_variant - - - - - - DISTANCE=540 rs198927 21:31979972 A - - - intergenic_variant - - - - - - rs198929 21:31981149 T 337966 NM_181602.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4856 rs198929 21:31981149 T CCDS13602.1 CCDS13602.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4859 rs1627036 21:31994251 C 100151643 NR_023342.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1082 rs1627123 21:31994281 C 100151643 NR_023342.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1112 rs8130002 21:32199412 C 337878 NM_181606.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1945 rs4817358 21:32210805 A - - - intergenic_variant - - - - - - rs2040128 21:32330004 A - - - intergenic_variant - - - - - - rs10854335 21:32349294 C - - - intergenic_variant - - - - - - rs8134880 21:32362549 A - - - intergenic_variant - - - - - - rs4817372 21:32370012 T - - - intergenic_variant - - - - - - rs4816382 21:32411041 A 728299 NM_001099219.1 Transcript upstream_gene_variant - - - - - - DISTANCE=246 rs4816382 21:32411041 A ENSESTG00000010111 ENSESTT00000025297 Transcript upstream_gene_variant - - - - - - DISTANCE=147 rs4816382 21:32411041 A CCDS42917.1 CCDS42917.1 Transcript upstream_gene_variant - - - - - - DISTANCE=279 rs845976 21:32622516 A ENSESTG00000028501 ENSESTT00000071781 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs845976 21:32622516 A ENSESTG00000028501 ENSESTT00000071678 Transcript intron_variant - - - - - - rs845976 21:32622516 A 7074 NM_003253.2 Transcript intron_variant - - - - - - rs845976 21:32622516 A CCDS13609.1 CCDS13609.1 Transcript intron_variant - - - - - - rs845975 21:32625558 G ENSESTG00000028501 ENSESTT00000071781 Transcript intron_variant - - - - - - rs845975 21:32625558 G ENSESTG00000028501 ENSESTT00000071678 Transcript intron_variant - - - - - - rs845975 21:32625558 G 7074 NM_003253.2 Transcript intron_variant - - - - - - rs845975 21:32625558 G CCDS13609.1 CCDS13609.1 Transcript intron_variant - - - - - - rs845932 21:32717597 A ENSESTG00000028501 ENSESTT00000071773 Transcript upstream_gene_variant - - - - - - DISTANCE=1003 rs845932 21:32717597 A ENSESTG00000028501 ENSESTT00000071678 Transcript intron_variant - - - - - - rs845932 21:32717597 A 7074 NM_003253.2 Transcript intron_variant - - - - - - rs845932 21:32717597 A ENSESTG00000028501 ENSESTT00000071759 Transcript upstream_gene_variant - - - - - - DISTANCE=908 rs845932 21:32717597 A ENSESTG00000028501 ENSESTT00000071717 Transcript intron_variant - - - - - - rs845932 21:32717597 A ENSESTG00000028501 ENSESTT00000071710 Transcript intron_variant - - - - - - rs1783090 21:32725534 G ENSESTG00000028501 ENSESTT00000071678 Transcript intron_variant - - - - - - rs1783090 21:32725534 G 7074 NM_003253.2 Transcript intron_variant - - - - - - rs1783090 21:32725534 G ENSESTG00000028501 ENSESTT00000071717 Transcript intron_variant - - - - - - rs1783090 21:32725534 G ENSESTG00000028501 ENSESTT00000071710 Transcript intron_variant - - - - - - rs531159 21:32744884 C ENSESTG00000028501 ENSESTT00000071678 Transcript intron_variant - - - - - - rs531159 21:32744884 C 7074 NM_003253.2 Transcript intron_variant - - - - - - rs531159 21:32744884 C ENSESTG00000028501 ENSESTT00000071717 Transcript intron_variant - - - - - - rs531159 21:32744884 C ENSESTG00000028501 ENSESTT00000071710 Transcript intron_variant - - - - - - rs480467 21:32776735 C ENSESTG00000028501 ENSESTT00000071678 Transcript intron_variant - - - - - - rs480467 21:32776735 C 7074 NM_003253.2 Transcript intron_variant - - - - - - rs480467 21:32776735 C ENSESTG00000028501 ENSESTT00000071717 Transcript intron_variant - - - - - - rs480467 21:32776735 C ENSESTG00000028501 ENSESTT00000071710 Transcript intron_variant - - - - - - rs579150 21:32788621 C ENSESTG00000028501 ENSESTT00000071678 Transcript intron_variant - - - - - - rs579150 21:32788621 C 7074 NM_003253.2 Transcript intron_variant - - - - - - rs579150 21:32788621 C ENSESTG00000028501 ENSESTT00000071717 Transcript intron_variant - - - - - - rs579150 21:32788621 C ENSESTG00000028501 ENSESTT00000071710 Transcript intron_variant - - - - - - rs553515 21:32826270 C ENSESTG00000028501 ENSESTT00000071678 Transcript intron_variant - - - - - - rs553515 21:32826270 C 7074 NM_003253.2 Transcript intron_variant - - - - - - rs553515 21:32826270 C ENSESTG00000028501 ENSESTT00000071717 Transcript intron_variant - - - - - - rs553515 21:32826270 C ENSESTG00000028501 ENSESTT00000071710 Transcript intron_variant - - - - - - rs8131447 21:32850711 T ENSESTG00000028501 ENSESTT00000071678 Transcript intron_variant - - - - - - rs8131447 21:32850711 T 7074 NM_003253.2 Transcript intron_variant - - - - - - rs8131447 21:32850711 T ENSESTG00000028501 ENSESTT00000071710 Transcript intron_variant - - - - - - rs7279602 21:32972108 A - - - intergenic_variant - - - - - - rs4817419 21:33007760 G - - - intergenic_variant - - - - - - rs204734 21:33073985 C ENSESTG00000028424 ENSESTT00000071506 Transcript intron_variant - - - - - - rs204734 21:33073985 C 57466 NM_001145444.1 Transcript intron_variant - - - - - - rs204734 21:33073985 C CCDS33537.1 CCDS33537.1 Transcript intron_variant - - - - - - rs204734 21:33073985 C ENSESTG00000028402 ENSESTT00000071403 Transcript downstream_gene_variant - - - - - - DISTANCE=3757 rs204734 21:33073985 C ENSESTG00000028424 ENSESTT00000071481 Transcript intron_variant - - - - - - rs204734 21:33073985 C CCDS46644.1 CCDS46644.1 Transcript intron_variant - - - - - - rs204734 21:33073985 C CCDS54482.1 CCDS54482.1 Transcript intron_variant - - - - - - rs204734 21:33073985 C 57466 NM_020706.2 Transcript intron_variant - - - - - - rs204734 21:33073985 C 57466 NM_001145445.1 Transcript intron_variant - - - - - - rs204729 21:33110144 A - ENSR00000315876 RegulatoryFeature regulatory_region_variant - - - - - - rs204729 21:33110144 A - - - intergenic_variant - - - - - - rs1783285 21:33154395 G - - - intergenic_variant - - - - - - rs9982019 21:33235445 A - - - intergenic_variant - - - - - - rs7279016 21:33280563 G - ENSR00001051151 RegulatoryFeature regulatory_region_variant - - - - - - rs7279016 21:33280563 G CCDS13610.1 CCDS13610.1 Transcript intron_variant - - - - - - rs7279016 21:33280563 G ENSESTG00000028324 ENSESTT00000071297 Transcript intron_variant - - - - - - rs7279016 21:33280563 G ENSESTG00000028324 ENSESTT00000071305 Transcript intron_variant - - - - - - rs7279016 21:33280563 G 30811 NM_014586.1 Transcript intron_variant - - - - - - rs2009194 21:33294710 C CCDS13610.1 CCDS13610.1 Transcript intron_variant - - - - - - rs2009194 21:33294710 C ENSESTG00000028324 ENSESTT00000071297 Transcript intron_variant - - - - - - rs2009194 21:33294710 C ENSESTG00000028324 ENSESTT00000071305 Transcript intron_variant - - - - - - rs2009194 21:33294710 C 30811 NM_014586.1 Transcript intron_variant - - - - - - rs7276738 21:33410344 C - - - intergenic_variant - - - - - - rs4817451 21:33439736 C - - - intergenic_variant - - - - - - rs2409439 21:33468996 C - ENSR00001566218 RegulatoryFeature regulatory_region_variant - - - - - - rs2409439 21:33468996 C - - - intergenic_variant - - - - - - rs2008743 21:33484483 G - - - intergenic_variant - - - - - - rs9984534 21:33528548 C - - - intergenic_variant - - - - - - rs7276534 21:33595178 G - - - intergenic_variant - - - - - - rs7280737 21:33624392 G - - - intergenic_variant - - - - - - rs7277047 21:33658482 A ENSESTG00000016852 ENSESTT00000042323 Transcript intron_variant - - - - - - rs9305501 21:33714265 A 9875 NM_014825.2 Transcript intron_variant - - - - - - rs9305501 21:33714265 A CCDS46645.1 CCDS46645.1 Transcript intron_variant - - - - - - rs9305501 21:33714265 A ENSESTG00000016815 ENSESTT00000042300 Transcript intron_variant - - - - - - rs9981211 21:33847327 C - ENSR00000684149 RegulatoryFeature regulatory_region_variant - - - - - - rs9981211 21:33847327 C ENSESTG00000016507 ENSESTT00000041401 Transcript intron_variant - - - - - - rs9981211 21:33847327 C 59271 NM_058187.3 Transcript intron_variant - - - - - - rs9981211 21:33847327 C ENSESTG00000016507 ENSESTT00000041417 Transcript intron_variant - - - - - - rs9981211 21:33847327 C CCDS13614.1 CCDS13614.1 Transcript intron_variant - - - - - - rs9981211 21:33847327 C ENSESTG00000016507 ENSESTT00000041389 Transcript intron_variant - - - - - - rs10775649 21:33853257 G ENSESTG00000016507 ENSESTT00000041401 Transcript intron_variant - - - - - - rs10775649 21:33853257 G 59271 NM_058187.3 Transcript intron_variant - - - - - - rs10775649 21:33853257 G ENSESTG00000016507 ENSESTT00000041417 Transcript intron_variant - - - - - - rs10775649 21:33853257 G CCDS13614.1 CCDS13614.1 Transcript intron_variant - - - - - - rs10775649 21:33853257 G ENSESTG00000016507 ENSESTT00000041389 Transcript intron_variant - - - - - - rs9305505 21:33919718 G - - - intergenic_variant - - - - - - rs860076 21:33976897 G - ENSR00000612860 RegulatoryFeature regulatory_region_variant - - - - - - rs860076 21:33976897 G ENSESTG00000016744 ENSESTT00000042118 Transcript upstream_gene_variant - - - - - - DISTANCE=1375 rs860076 21:33976897 G 56683 NR_036552.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs860076 21:33976897 G ENSESTG00000016744 ENSESTT00000042112 Transcript upstream_gene_variant - - - - - - DISTANCE=1369 rs860076 21:33976897 G CCDS13617.1 CCDS13617.1 Transcript intron_variant - - - - - - rs860076 21:33976897 G ENSESTG00000016541 ENSESTT00000041477 Transcript intron_variant - - - - - - rs860076 21:33976897 G 56683 NM_021254.2 Transcript intron_variant - - - - - - rs860076 21:33976897 G ENSESTG00000016744 ENSESTT00000042104 Transcript intron_variant - - - - - - rs1782966 21:34080082 T 8867 NM_001160302.1 Transcript intron_variant - - - - - - rs1782966 21:34080082 T CCDS54483.1 CCDS54483.1 Transcript intron_variant - - - - - - rs1782966 21:34080082 T CCDS33540.2 CCDS33540.2 Transcript intron_variant - - - - - - rs1782966 21:34080082 T 8867 NM_003895.3 Transcript intron_variant - - - - - - rs1782966 21:34080082 T ENSESTG00000016657 ENSESTT00000041783 Transcript intron_variant - - - - - - rs1782966 21:34080082 T 8867 NM_001160306.1 Transcript intron_variant - - - - - - rs1782966 21:34080082 T CCDS54484.1 CCDS54484.1 Transcript intron_variant - - - - - - rs1782966 21:34080082 T ENSESTG00000016657 ENSESTT00000041779 Transcript intron_variant - - - - - - rs1782966 21:34080082 T 8867 NM_203446.2 Transcript intron_variant - - - - - - rs1782966 21:34080082 T ENSESTG00000016657 ENSESTT00000041755 Transcript intron_variant - - - - - - rs1782966 21:34080082 T CCDS33539.2 CCDS33539.2 Transcript intron_variant - - - - - - rs609245 21:34104794 A 8867 NM_001160302.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4544 rs609245 21:34104794 A ENSESTG00000016580 ENSESTT00000041670 Transcript downstream_gene_variant - - - - - - DISTANCE=4857 rs609245 21:34104794 A ENSESTG00000016549 ENSESTT00000041499 Transcript intron_variant - - - - - - rs609245 21:34104794 A CCDS13619.1 CCDS13619.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2467 rs609245 21:34104794 A 100506215 NR_038880.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs609245 21:34104794 A 8867 NM_203446.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4443 rs609245 21:34104794 A 100506215 NR_038879.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs609245 21:34104794 A ENSESTG00000016657 ENSESTT00000041755 Transcript upstream_gene_variant - - - - - - DISTANCE=4447 rs609245 21:34104794 A 94104 NM_016631.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1416 rs609245 21:34104794 A CCDS33540.2 CCDS33540.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4443 rs609245 21:34104794 A 8867 NM_003895.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4443 rs609245 21:34104794 A 8867 NM_001160306.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4544 rs609245 21:34104794 A 94104 NR_027873.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1416 rs609245 21:34104794 A ENSESTG00000016657 ENSESTT00000041779 Transcript upstream_gene_variant - - - - - - DISTANCE=4544 rs609245 21:34104794 A ENSESTG00000016580 ENSESTT00000041684 Transcript downstream_gene_variant - - - - - - DISTANCE=4859 rs609245 21:34104794 A CCDS33539.2 CCDS33539.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4443 rs2186271 21:34116555 A 94104 NM_016631.3 Transcript intron_variant - - - - - - rs2186271 21:34116555 A CCDS33541.1 CCDS33541.1 Transcript intron_variant - - - - - - rs2186271 21:34116555 A ENSESTG00000016580 ENSESTT00000041670 Transcript intron_variant - - - - - - rs2186271 21:34116555 A ENSESTG00000016580 ENSESTT00000041726 Transcript intron_variant - - - - - - rs2186271 21:34116555 A ENSESTG00000016580 ENSESTT00000041721 Transcript intron_variant - - - - - - rs2186271 21:34116555 A CCDS13619.1 CCDS13619.1 Transcript intron_variant - - - - - - rs2186271 21:34116555 A 94104 NM_013329.3 Transcript intron_variant - - - - - - rs2186271 21:34116555 A 94104 NR_027873.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2186271 21:34116555 A ENSESTG00000016580 ENSESTT00000041717 Transcript intron_variant - - - - - - rs2186271 21:34116555 A ENSESTG00000016580 ENSESTT00000041684 Transcript intron_variant - - - - - - rs2186271 21:34116555 A 100506215 NR_038879.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1122 rs7276788 21:34405797 C - ENSR00000612889 RegulatoryFeature regulatory_region_variant - - - - - - rs7276788 21:34405797 C 10215 NM_005806.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4293 rs7276788 21:34405797 C ENSESTG00000016562 ENSESTT00000041521 Transcript intron_variant - - - - - - rs9979768 21:34415248 A - ENSR00000612892 RegulatoryFeature regulatory_region_variant - - - - - - rs9979768 21:34415248 A ENSESTG00000016562 ENSESTT00000041521 Transcript intron_variant - - - - - - rs2843693 21:34571365 T - ENSR00001566304 RegulatoryFeature regulatory_region_variant - - - - - - rs2843693 21:34571365 T - - - intergenic_variant - - - - - - rs6517155 21:34628320 C ENSESTG00000010100 ENSESTT00000025331 Transcript intron_variant - - - - - - rs6517155 21:34628320 C ENSESTG00000010100 ENSESTT00000025309 Transcript intron_variant - - - - - - rs6517155 21:34628320 C 3455 NM_207584.1 Transcript intron_variant - - - - - - rs6517155 21:34628320 C 3455 NM_000874.3 Transcript intron_variant - - - - - - rs6517155 21:34628320 C ENSESTG00000010100 ENSESTT00000025335 Transcript intron_variant - - - - - - rs6517155 21:34628320 C 3455 NM_207585.1 Transcript intron_variant - - - - - - rs6517155 21:34628320 C ENSESTG00000010100 ENSESTT00000025338 Transcript intron_variant - - - - - - rs6517155 21:34628320 C CCDS13622.1 CCDS13622.1 Transcript intron_variant - - - - - - rs6517155 21:34628320 C ENSESTG00000010100 ENSESTT00000025326 Transcript intron_variant - - - - - - rs6517155 21:34628320 C CCDS13621.1 CCDS13621.1 Transcript intron_variant - - - - - - rs2247703 21:34743800 T - - - intergenic_variant - - - - - - rs8127270 21:34779062 T CCDS33544.1 CCDS33544.1 Transcript intron_variant - - - - - - rs8127270 21:34779062 T ENSESTG00000010204 ENSESTT00000025535 Transcript intron_variant - - - - - - rs8127270 21:34779062 T 3460 NM_005534.3 Transcript intron_variant - - - - - - rs8127270 21:34779062 T ENSESTG00000010204 ENSESTT00000025538 Transcript intron_variant - - - - - - rs4817578 21:34899328 C 2618 NM_175085.2 Transcript intron_variant - - - - - - rs4817578 21:34899328 C 2618 NM_001136005.1 Transcript intron_variant - - - - - - rs4817578 21:34899328 C 2618 NM_000819.4 Transcript intron_variant - - - - - - rs4817578 21:34899328 C CCDS13627.1 CCDS13627.1 Transcript intron_variant - - - - - - rs4817578 21:34899328 C CCDS13628.1 CCDS13628.1 Transcript intron_variant - - - - - - rs4817578 21:34899328 C 2618 NM_001136006.1 Transcript intron_variant - - - - - - rs762186 21:35242393 T CCDS33545.1 CCDS33545.1 Transcript intron_variant - - - - - - rs762186 21:35242393 T 6453 NM_003024.2 Transcript intron_variant - - - - - - rs6517201 21:35417576 T - - - intergenic_variant - - - - - - rs9983736 21:35462018 G ENSESTG00000008276 ENSESTT00000020886 Transcript intron_variant - - - - - - rs9983736 21:35462018 G ENSESTG00000008480 ENSESTT00000021355 Transcript downstream_gene_variant - - - - - - DISTANCE=3559 rs9983736 21:35462018 G ENSESTG00000008276 ENSESTT00000020956 Transcript intron_variant - - - - - - rs9983736 21:35462018 G ENSESTG00000008276 ENSESTT00000020979 Transcript intron_variant - - - - - - rs9983736 21:35462018 G ENSESTG00000008276 ENSESTT00000020963 Transcript intron_variant - - - - - - rs9983736 21:35462018 G ENSESTG00000008276 ENSESTT00000020935 Transcript intron_variant - - - - - - rs9983736 21:35462018 G ENSESTG00000008276 ENSESTT00000020920 Transcript intron_variant - - - - - - rs9983736 21:35462018 G 64968 NM_032476.3 Transcript intron_variant - - - - - - rs9983736 21:35462018 G CCDS33548.1 CCDS33548.1 Transcript intron_variant - - - - - - rs9983736 21:35462018 G 6526 NM_006933.4 Transcript intron_variant - - - - - - rs9984054 21:35462128 C ENSESTG00000008276 ENSESTT00000020886 Transcript intron_variant - - - - - - rs9984054 21:35462128 C ENSESTG00000008480 ENSESTT00000021355 Transcript downstream_gene_variant - - - - - - DISTANCE=3449 rs9984054 21:35462128 C ENSESTG00000008276 ENSESTT00000020956 Transcript intron_variant - - - - - - rs9984054 21:35462128 C ENSESTG00000008276 ENSESTT00000020979 Transcript intron_variant - - - - - - rs9984054 21:35462128 C ENSESTG00000008276 ENSESTT00000020963 Transcript intron_variant - - - - - - rs9984054 21:35462128 C ENSESTG00000008276 ENSESTT00000020935 Transcript intron_variant - - - - - - rs9984054 21:35462128 C ENSESTG00000008276 ENSESTT00000020920 Transcript intron_variant - - - - - - rs9984054 21:35462128 C 64968 NM_032476.3 Transcript intron_variant - - - - - - rs9984054 21:35462128 C CCDS33548.1 CCDS33548.1 Transcript intron_variant - - - - - - rs9984054 21:35462128 C 6526 NM_006933.4 Transcript intron_variant - - - - - - rs2154504 21:35463640 T ENSESTG00000008276 ENSESTT00000020886 Transcript intron_variant - - - - - - rs2154504 21:35463640 T ENSESTG00000008480 ENSESTT00000021355 Transcript downstream_gene_variant - - - - - - DISTANCE=1937 rs2154504 21:35463640 T ENSESTG00000008276 ENSESTT00000020956 Transcript intron_variant - - - - - - rs2154504 21:35463640 T ENSESTG00000008276 ENSESTT00000020979 Transcript intron_variant - - - - - - rs2154504 21:35463640 T ENSESTG00000008276 ENSESTT00000020963 Transcript intron_variant - - - - - - rs2154504 21:35463640 T CCDS33549.1 CCDS33549.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3858 rs2154504 21:35463640 T ENSESTG00000008276 ENSESTT00000020935 Transcript intron_variant - - - - - - rs2154504 21:35463640 T ENSESTG00000008276 ENSESTT00000020920 Transcript intron_variant - - - - - - rs2154504 21:35463640 T 64968 NM_032476.3 Transcript intron_variant - - - - - - rs2154504 21:35463640 T CCDS33548.1 CCDS33548.1 Transcript intron_variant - - - - - - rs2154504 21:35463640 T 6526 NM_006933.4 Transcript intron_variant - - - - - - rs8129891 21:35467645 G ENSESTG00000008276 ENSESTT00000020886 Transcript missense_variant 550 148 50 T/A Aca/Gca - rs8129891 21:35467645 G ENSESTG00000008480 ENSESTT00000021355 Transcript intron_variant - - - - - - rs8129891 21:35467645 G ENSESTG00000008276 ENSESTT00000020956 Transcript intron_variant - - - - - - rs8129891 21:35467645 G ENSESTG00000008276 ENSESTT00000020979 Transcript missense_variant 652 148 50 T/A Aca/Gca - rs8129891 21:35467645 G ENSESTG00000008276 ENSESTT00000020963 Transcript intron_variant - - - - - - rs8129891 21:35467645 G CCDS33549.1 CCDS33549.1 Transcript missense_variant 148 148 50 T/A Aca/Gca - PolyPhen=benign;SIFT=tolerated rs8129891 21:35467645 G ENSESTG00000008276 ENSESTT00000020935 Transcript intron_variant - - - - - - rs8129891 21:35467645 G ENSESTG00000008276 ENSESTT00000020920 Transcript intron_variant - - - - - - rs8129891 21:35467645 G 64968 NM_032476.3 Transcript intron_variant - - - - - - rs8129891 21:35467645 G CCDS33548.1 CCDS33548.1 Transcript intron_variant - - - - - - rs8129891 21:35467645 G 6526 NM_006933.4 Transcript missense_variant 660 148 50 T/A Aca/Gca - PolyPhen=benign;SIFT=tolerated rs4817617 21:35469193 A ENSESTG00000008276 ENSESTT00000020886 Transcript downstream_gene_variant - - - - - - DISTANCE=1523 rs4817617 21:35469193 A ENSESTG00000008480 ENSESTT00000021355 Transcript intron_variant - - - - - - rs4817617 21:35469193 A ENSESTG00000008276 ENSESTT00000020956 Transcript intron_variant - - - - - - rs4817617 21:35469193 A ENSESTG00000008276 ENSESTT00000020979 Transcript downstream_gene_variant - - - - - - DISTANCE=1384 rs4817617 21:35469193 A ENSESTG00000008276 ENSESTT00000020963 Transcript intron_variant - - - - - - rs4817617 21:35469193 A CCDS33549.1 CCDS33549.1 Transcript missense_variant 1696 1696 566 Q/K Caa/Aaa - PolyPhen=benign;SIFT=tolerated rs4817617 21:35469193 A ENSESTG00000008276 ENSESTT00000020935 Transcript intron_variant - - - - - - rs4817617 21:35469193 A ENSESTG00000008276 ENSESTT00000020920 Transcript intron_variant - - - - - - rs4817617 21:35469193 A 64968 NM_032476.3 Transcript intron_variant - - - - - - rs4817617 21:35469193 A CCDS33548.1 CCDS33548.1 Transcript intron_variant - - - - - - rs4817617 21:35469193 A 6526 NM_006933.4 Transcript missense_variant 2208 1696 566 Q/K Caa/Aaa - PolyPhen=benign;SIFT=tolerated rs4817619 21:35470042 T ENSESTG00000008276 ENSESTT00000020886 Transcript downstream_gene_variant - - - - - - DISTANCE=2372 rs4817619 21:35470042 T ENSESTG00000008480 ENSESTT00000021355 Transcript intron_variant - - - - - - rs4817619 21:35470042 T ENSESTG00000008276 ENSESTT00000020956 Transcript intron_variant - - - - - - rs4817619 21:35470042 T ENSESTG00000008276 ENSESTT00000020979 Transcript downstream_gene_variant - - - - - - DISTANCE=2233 rs4817619 21:35470042 T ENSESTG00000008276 ENSESTT00000020963 Transcript intron_variant - - - - - - rs4817619 21:35470042 T CCDS33549.1 CCDS33549.1 Transcript downstream_gene_variant - - - - - - DISTANCE=388 rs4817619 21:35470042 T ENSESTG00000008276 ENSESTT00000020935 Transcript intron_variant - - - - - - rs4817619 21:35470042 T ENSESTG00000008276 ENSESTT00000020920 Transcript intron_variant - - - - - - rs4817619 21:35470042 T 64968 NM_032476.3 Transcript intron_variant - - - - - - rs4817619 21:35470042 T CCDS33548.1 CCDS33548.1 Transcript intron_variant - - - - - - rs4817619 21:35470042 T 6526 NM_006933.4 Transcript 3_prime_UTR_variant 3057 - - - - - rs2409518 21:35581907 T - - - intergenic_variant - - - - - - rs4817647 21:35731589 T 9992 NM_172201.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4734 rs4817647 21:35731589 T ENSESTG00000008323 ENSESTT00000021005 Transcript upstream_gene_variant - - - - - - DISTANCE=4734 rs2012713 21:35761950 G ENSESTG00000008332 ENSESTT00000021047 Transcript downstream_gene_variant - - - - - - DISTANCE=508 rs2012713 21:35761950 G ENSESTG00000008332 ENSESTT00000021084 Transcript intron_variant - - - - - - rs2012713 21:35761950 G 54065 NM_058182.4 Transcript downstream_gene_variant - - - - - - DISTANCE=498 rs2012713 21:35761950 G CCDS33550.1 CCDS33550.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4010 rs2012713 21:35761950 G ENSESTG00000008332 ENSESTT00000021065 Transcript intron_variant - - - - - - rs2154439 21:35764459 A ENSESTG00000008332 ENSESTT00000021047 Transcript downstream_gene_variant - - - - - - DISTANCE=3017 rs2154439 21:35764459 A ENSESTG00000008332 ENSESTT00000021084 Transcript intron_variant - - - - - - rs2154439 21:35764459 A 54065 NM_058182.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3007 rs2154439 21:35764459 A ENSESTG00000008332 ENSESTT00000021065 Transcript intron_variant - - - - - - rs9981933 21:35765774 C ENSESTG00000008332 ENSESTT00000021047 Transcript downstream_gene_variant - - - - - - DISTANCE=4332 rs9981933 21:35765774 C ENSESTG00000008332 ENSESTT00000021084 Transcript intron_variant - - - - - - rs9981933 21:35765774 C 54065 NM_058182.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4322 rs9981933 21:35765774 C ENSESTG00000008332 ENSESTT00000021065 Transcript intron_variant - - - - - - rs2211696 21:35819536 G - ENSR00001051189 RegulatoryFeature regulatory_region_variant - - - - - - rs2211696 21:35819536 G 3753 NM_001270402.1 Transcript 3_prime_UTR_variant 2797 - - - - - rs2211696 21:35819536 G ENSESTG00000008467 ENSESTT00000021342 Transcript downstream_gene_variant - - - - - - DISTANCE=2053 rs2211696 21:35819536 G ENSESTG00000008467 ENSESTT00000021340 Transcript downstream_gene_variant - - - - - - DISTANCE=2031 rs2211696 21:35819536 G 3753 NM_001270405.1 Transcript 3_prime_UTR_variant 2598 - - - - - rs2211696 21:35819536 G 3753 NM_001127669.2 Transcript 3_prime_UTR_variant 2606 - - - - - rs2211696 21:35819536 G ENSESTG00000008467 ENSESTT00000021325 Transcript downstream_gene_variant - - - - - - DISTANCE=2060 rs2211696 21:35819536 G CCDS13636.1 CCDS13636.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2007 rs2211696 21:35819536 G 3753 NM_000219.4 Transcript 3_prime_UTR_variant 3022 - - - - - rs2211696 21:35819536 G 3753 NM_001270403.1 Transcript 3_prime_UTR_variant 2745 - - - - - rs2211696 21:35819536 G 3753 NM_001127668.2 Transcript 3_prime_UTR_variant 2634 - - - - - rs2211696 21:35819536 G 3753 NM_001127670.2 Transcript 3_prime_UTR_variant 2871 - - - - - rs2211696 21:35819536 G ENSESTG00000008467 ENSESTT00000021345 Transcript downstream_gene_variant - - - - - - DISTANCE=2329 rs2211696 21:35819536 G ENSESTG00000008467 ENSESTT00000021333 Transcript downstream_gene_variant - - - - - - DISTANCE=2112 rs2211696 21:35819536 G 3753 NM_001270404.1 Transcript 3_prime_UTR_variant 2686 - - - - - rs6517240 21:35902861 A - ENSR00000316039 RegulatoryFeature regulatory_region_variant - - - - - - rs6517240 21:35902861 A ENSESTG00000008437 ENSESTT00000021300 Transcript upstream_gene_variant - - - - - - DISTANCE=3741 rs6517240 21:35902861 A ENSESTG00000008437 ENSESTT00000021273 Transcript intron_variant - - - - - - rs6517240 21:35902861 A CCDS33551.1 CCDS33551.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3814 rs6517240 21:35902861 A CCDS13637.1 CCDS13637.1 Transcript intron_variant - - - - - - rs6517240 21:35902861 A 1827 NM_203417.1 Transcript intron_variant - - - - - - rs6517240 21:35902861 A 1827 NM_203418.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3600 rs6517240 21:35902861 A 1827 NM_004414.5 Transcript intron_variant - - - - - - rs2096470 21:36010099 T - - - intergenic_variant - - - - - - rs1009925 21:36049369 C 54102 NM_053277.1 Transcript intron_variant - - - - - - rs1009925 21:36049369 C CCDS13638.1 CCDS13638.1 Transcript intron_variant - - - - - - rs984187 21:36140761 T 100506385 NR_038885.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7281988 21:36153364 T 100506385 NR_038885.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2012247 21:36218373 C - ENSR00001566463 RegulatoryFeature regulatory_region_variant - - - - - - rs2012247 21:36218373 C 861 NM_001122607.1 Transcript intron_variant - - - - - - rs2012247 21:36218373 C 861 NM_001001890.2 Transcript intron_variant - - - - - - rs2012247 21:36218373 C ENSESTG00000008379 ENSESTT00000021139 Transcript intron_variant - - - - - - rs2012247 21:36218373 C 861 NM_001754.4 Transcript intron_variant - - - - - - rs2012247 21:36218373 C CCDS42922.1 CCDS42922.1 Transcript intron_variant - - - - - - rs2012247 21:36218373 C ENSESTG00000008379 ENSESTT00000021148 Transcript downstream_gene_variant - - - - - - DISTANCE=4925 rs2012247 21:36218373 C ENSESTG00000008397 ENSESTT00000021229 Transcript intron_variant - - - - - - rs2012247 21:36218373 C ENSESTG00000008379 ENSESTT00000021152 Transcript downstream_gene_variant - - - - - - DISTANCE=4956 rs2012247 21:36218373 C CCDS46646.1 CCDS46646.1 Transcript intron_variant - - - - - - rs2012247 21:36218373 C ENSESTG00000008397 ENSESTT00000021223 Transcript intron_variant - - - - - - rs2012247 21:36218373 C ENSESTG00000008397 ENSESTT00000021239 Transcript intron_variant - - - - - - rs2012247 21:36218373 C CCDS13639.1 CCDS13639.1 Transcript intron_variant - - - - - - rs6517259 21:36228390 T 861 NM_001122607.1 Transcript intron_variant - - - - - - rs6517259 21:36228390 T 861 NM_001001890.2 Transcript intron_variant - - - - - - rs6517259 21:36228390 T ENSESTG00000008379 ENSESTT00000021139 Transcript intron_variant - - - - - - rs6517259 21:36228390 T 861 NM_001754.4 Transcript intron_variant - - - - - - rs6517259 21:36228390 T CCDS42922.1 CCDS42922.1 Transcript intron_variant - - - - - - rs6517259 21:36228390 T ENSESTG00000008397 ENSESTT00000021229 Transcript intron_variant - - - - - - rs6517259 21:36228390 T CCDS46646.1 CCDS46646.1 Transcript intron_variant - - - - - - rs6517259 21:36228390 T ENSESTG00000008397 ENSESTT00000021223 Transcript intron_variant - - - - - - rs6517259 21:36228390 T ENSESTG00000008397 ENSESTT00000021239 Transcript intron_variant - - - - - - rs6517259 21:36228390 T CCDS13639.1 CCDS13639.1 Transcript intron_variant - - - - - - rs2843967 21:36265831 T ENSESTG00000008379 ENSESTT00000021139 Transcript intron_variant - - - - - - rs2843967 21:36265831 T ENSESTG00000008397 ENSESTT00000021180 Transcript intron_variant - - - - - - rs2843967 21:36265831 T 861 NM_001754.4 Transcript intron_variant - - - - - - rs2843967 21:36265831 T 861 NM_001122607.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4844 rs2843967 21:36265831 T 861 NM_001001890.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4844 rs2843967 21:36265831 T CCDS13639.1 CCDS13639.1 Transcript intron_variant - - - - - - rs1006638 21:36298020 A ENSESTG00000008379 ENSESTT00000021139 Transcript intron_variant - - - - - - rs1006638 21:36298020 A ENSESTG00000008397 ENSESTT00000021180 Transcript intron_variant - - - - - - rs1006638 21:36298020 A 861 NM_001754.4 Transcript intron_variant - - - - - - rs1006638 21:36298020 A CCDS13639.1 CCDS13639.1 Transcript intron_variant - - - - - - rs1984308 21:36349363 A ENSESTG00000008397 ENSESTT00000021180 Transcript intron_variant - - - - - - rs1984308 21:36349363 A 861 NM_001754.4 Transcript intron_variant - - - - - - rs1984308 21:36349363 A ENSESTG00000008397 ENSESTT00000021191 Transcript intron_variant - - - - - - rs1984308 21:36349363 A CCDS13639.1 CCDS13639.1 Transcript intron_variant - - - - - - rs58971095 21:36369578 C - ENSR00001051208 RegulatoryFeature regulatory_region_variant - - - - - - rs58971095 21:36369578 C ENSESTG00000008397 ENSESTT00000021180 Transcript intron_variant - - - - - - rs58971095 21:36369578 C 861 NM_001754.4 Transcript intron_variant - - - - - - rs58971095 21:36369578 C ENSESTG00000008397 ENSESTT00000021191 Transcript intron_variant - - - - - - rs58971095 21:36369578 C CCDS13639.1 CCDS13639.1 Transcript intron_variant - - - - - - rs7276529 21:36395288 C ENSESTG00000008397 ENSESTT00000021180 Transcript intron_variant - - - - - - rs7276529 21:36395288 C 861 NM_001754.4 Transcript intron_variant - - - - - - rs7276529 21:36395288 C ENSESTG00000028909 ENSESTT00000072779 Transcript intron_variant - - - - - - rs7276529 21:36395288 C ENSESTG00000008397 ENSESTT00000021191 Transcript intron_variant - - - - - - rs7276529 21:36395288 C CCDS13639.1 CCDS13639.1 Transcript intron_variant - - - - - - rs1976997 21:36441514 C ENSESTG00000028904 ENSESTT00000072741 Transcript upstream_gene_variant - - - - - - DISTANCE=4145 rs1883065 21:36464182 T - - - intergenic_variant - - - - - - rs2256809 21:36601299 A - ENSR00000316105 RegulatoryFeature regulatory_region_variant - - - - - - rs2256809 21:36601299 A - - - intergenic_variant - - - - - - rs2481858 21:36613237 G - - - intergenic_variant - - - - - - rs2481859 21:36616065 C - - - intergenic_variant - - - - - - rs2018769 21:36616507 T - - - intergenic_variant - - - - - - rs2471798 21:36620572 G - - - intergenic_variant - - - - - - rs8133319 21:36810074 T ENSESTG00000028893 ENSESTT00000072723 Transcript intron_variant - - - - - - rs9975880 21:36864025 C ENSESTG00000028893 ENSESTT00000072723 Transcript intron_variant - - - - - - rs1734508 21:37027434 C - - - intergenic_variant - - - - - - rs463127 21:37170313 A ENSESTG00000028890 ENSESTT00000072682 Transcript intron_variant - - - - - - rs4817758 21:37370538 A ENSESTG00000013298 ENSESTT00000033342 Transcript intron_variant - - - - - - rs4817758 21:37370538 A ENSESTG00000028884 ENSESTT00000072673 Transcript intron_variant - - - - - - rs8132842 21:37403267 C - ENSR00000316137 RegulatoryFeature regulatory_region_variant - - - - - - rs8132842 21:37403267 C 54093 NR_040087.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3573 rs8132842 21:37403267 C 54093 NR_040086.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3574 rs8132842 21:37403267 C 54093 NM_017438.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3572 rs7282629 21:37429679 C 54093 NM_001007259.1 Transcript intron_variant - - - - - - rs7282629 21:37429679 C ENSESTG00000013280 ENSESTT00000033319 Transcript intron_variant - - - - - - rs7282629 21:37429679 C CCDS13640.1 CCDS13640.1 Transcript intron_variant - - - - - - rs7282629 21:37429679 C ENSESTG00000013280 ENSESTT00000033336 Transcript upstream_gene_variant - - - - - - DISTANCE=80 rs7282629 21:37429679 C 54093 NM_017438.3 Transcript intron_variant - - - - - - rs7282629 21:37429679 C ENSESTG00000013280 ENSESTT00000033332 Transcript intron_variant - - - - - - rs7282629 21:37429679 C 54093 NR_040087.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7282629 21:37429679 C 54093 NR_040088.1 Transcript splice_region_variant,intron_variant,nc_transcript_variant - - - - - - rs7282629 21:37429679 C ENSESTG00000013280 ENSESTT00000033326 Transcript intron_variant - - - - - - rs7282629 21:37429679 C CCDS42923.1 CCDS42923.1 Transcript intron_variant - - - - - - rs7282629 21:37429679 C 54093 NR_040086.1 Transcript splice_region_variant,intron_variant,nc_transcript_variant - - - - - - rs7282629 21:37429679 C ENSESTG00000013280 ENSESTT00000033324 Transcript intron_variant - - - - - - rs2156409 21:37449677 C CCDS13641.1 CCDS13641.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4497 rs2156409 21:37449677 C 873 NM_001757.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4215 rs2156409 21:37449677 C 100133286 NR_040084.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2156409 21:37449677 C ENSESTG00000013121 ENSESTT00000032892 Transcript downstream_gene_variant - - - - - - DISTANCE=4213 rs9980801 21:37656409 C ENSESTG00000013153 ENSESTT00000033038 Transcript intron_variant - - - - - - rs9980801 21:37656409 C CCDS13643.1 CCDS13643.1 Transcript intron_variant - - - - - - rs9980801 21:37656409 C 9980 NM_005128.2 Transcript intron_variant - - - - - - rs9980801 21:37656409 C ENSESTG00000013153 ENSESTT00000033033 Transcript intron_variant - - - - - - rs9305603 21:38058814 C - - - intergenic_variant - - - - - - rs2845788 21:38100968 G CCDS46647.1 CCDS46647.1 Transcript intron_variant - - - - - - rs2845788 21:38100968 G 6493 NM_009586.2 Transcript intron_variant - - - - - - rs2845788 21:38100968 G ENSESTG00000013252 ENSESTT00000033229 Transcript upstream_gene_variant - - - - - - DISTANCE=2460 rs2845788 21:38100968 G CCDS13646.1 CCDS13646.1 Transcript intron_variant - - - - - - rs2845788 21:38100968 G 6493 NM_005069.3 Transcript intron_variant - - - - - - rs2026261 21:38107665 C CCDS46647.1 CCDS46647.1 Transcript intron_variant - - - - - - rs2026261 21:38107665 C 6493 NM_009586.2 Transcript intron_variant - - - - - - rs2026261 21:38107665 C ENSESTG00000013252 ENSESTT00000033229 Transcript intron_variant - - - - - - rs2026261 21:38107665 C CCDS13646.1 CCDS13646.1 Transcript intron_variant - - - - - - rs2026261 21:38107665 C 6493 NM_005069.3 Transcript intron_variant - - - - - - rs6517380 21:38136261 C 3141 NM_001242784.1 Transcript intron_variant - - - - - - rs6517380 21:38136261 C 3141 NM_001242785.1 Transcript intron_variant - - - - - - rs6517380 21:38136261 C CCDS13647.1 CCDS13647.1 Transcript intron_variant - - - - - - rs6517380 21:38136261 C ENSESTG00000013256 ENSESTT00000033248 Transcript intron_variant - - - - - - rs6517380 21:38136261 C 3141 NM_000411.6 Transcript intron_variant - - - - - - rs2898307 21:38210169 G 3141 NM_001242784.1 Transcript intron_variant - - - - - - rs2898307 21:38210169 G 3141 NM_001242785.1 Transcript intron_variant - - - - - - rs2898307 21:38210169 G CCDS13647.1 CCDS13647.1 Transcript intron_variant - - - - - - rs2898307 21:38210169 G ENSESTG00000013256 ENSESTT00000033248 Transcript intron_variant - - - - - - rs2898307 21:38210169 G 3141 NM_000411.6 Transcript intron_variant - - - - - - rs7281668 21:38227012 G - ENSR00000613529 RegulatoryFeature regulatory_region_variant - - - - - - rs7281668 21:38227012 G 3141 NM_001242784.1 Transcript intron_variant - - - - - - rs7281668 21:38227012 G 3141 NM_001242785.1 Transcript intron_variant - - - - - - rs7281668 21:38227012 G CCDS13647.1 CCDS13647.1 Transcript intron_variant - - - - - - rs7281668 21:38227012 G ENSESTG00000013256 ENSESTT00000033248 Transcript intron_variant - - - - - - rs7281668 21:38227012 G 3141 NM_000411.6 Transcript intron_variant - - - - - - rs4817825 21:38251573 G 3141 NM_001242784.1 Transcript intron_variant - - - - - - rs4817825 21:38251573 G 3141 NM_001242785.1 Transcript intron_variant - - - - - - rs4817825 21:38251573 G CCDS13647.1 CCDS13647.1 Transcript intron_variant - - - - - - rs4817825 21:38251573 G ENSESTG00000013256 ENSESTT00000033248 Transcript intron_variant - - - - - - rs4817825 21:38251573 G 3141 NM_000411.6 Transcript intron_variant - - - - - - rs28530 21:38352222 G ENSESTG00000029845 ENSESTT00000075097 Transcript intron_variant - - - - - - rs28530 21:38352222 G ENSESTG00000029845 ENSESTT00000075117 Transcript intron_variant - - - - - - rs28530 21:38352222 G 3141 NM_001242785.1 Transcript intron_variant - - - - - - rs28530 21:38352222 G ENSESTG00000029845 ENSESTT00000075141 Transcript intron_variant - - - - - - rs28530 21:38352222 G ENSESTG00000029845 ENSESTT00000075052 Transcript intron_variant - - - - - - rs28530 21:38352222 G 3141 NM_000411.6 Transcript intron_variant - - - - - - rs28530 21:38352222 G ENSESTG00000029845 ENSESTT00000075166 Transcript intron_variant - - - - - - rs2507733 21:38444863 T - ENSR00000106776 RegulatoryFeature regulatory_region_variant - - - - - - rs2507733 21:38444863 T ENSESTG00000029041 ENSESTT00000073832 Transcript upstream_gene_variant - - - - - - DISTANCE=621 rs2507733 21:38444863 T 51227 NM_153682.2 Transcript intron_variant - - - - - - rs2507733 21:38444863 T 51227 NM_153681.2 Transcript missense_variant 241 25 9 A/T Gcg/Acg - PolyPhen=benign;SIFT=tolerated rs2507733 21:38444863 T ENSESTG00000029041 ENSESTT00000073857 Transcript upstream_gene_variant - - - - - - DISTANCE=621 rs2507733 21:38444863 T ENSESTG00000029041 ENSESTT00000074036 Transcript upstream_gene_variant - - - - - - DISTANCE=704 rs2507733 21:38444863 T CCDS13649.1 CCDS13649.1 Transcript missense_variant 25 25 9 A/T Gcg/Acg - PolyPhen=benign;SIFT=tolerated rs2507733 21:38444863 T CCDS13650.1 CCDS13650.1 Transcript upstream_gene_variant - - - - - - DISTANCE=48 rs2507733 21:38444863 T 7267 NM_001001894.1 Transcript upstream_gene_variant - - - - - - DISTANCE=708 rs2507733 21:38444863 T ENSESTG00000029041 ENSESTT00000074056 Transcript upstream_gene_variant - - - - - - DISTANCE=704 rs2507733 21:38444863 T ENSESTG00000029826 ENSESTT00000075022 Transcript missense_variant 160 25 9 A/T Gcg/Acg - rs2507733 21:38444863 T ENSESTG00000029041 ENSESTT00000074071 Transcript upstream_gene_variant - - - - - - DISTANCE=759 rs2507733 21:38444863 T 51227 NR_028352.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2507733 21:38444863 T ENSESTG00000029041 ENSESTT00000073824 Transcript upstream_gene_variant - - - - - - DISTANCE=621 rs2507733 21:38444863 T ENSESTG00000029041 ENSESTT00000074048 Transcript upstream_gene_variant - - - - - - DISTANCE=704 rs1787364 21:38527742 G - ENSR00001566738 RegulatoryFeature regulatory_region_variant - - - - - - rs1787364 21:38527742 G ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1787364 21:38527742 G CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1787364 21:38527742 G 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1787364 21:38527742 G ENSESTG00000029041 ENSESTT00000074108 Transcript upstream_gene_variant - - - - - - DISTANCE=1335 rs1787364 21:38527742 G ENSESTG00000029041 ENSESTT00000073857 Transcript downstream_gene_variant - - - - - - DISTANCE=3499 rs1787364 21:38527742 G ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1787364 21:38527742 G 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1787364 21:38527742 G ENSESTG00000029041 ENSESTT00000074056 Transcript downstream_gene_variant - - - - - - DISTANCE=3499 rs1787364 21:38527742 G ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1787364 21:38527742 G ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs1793878 21:38531355 C - ENSR00001051241 RegulatoryFeature regulatory_region_variant - - - - - - rs1793878 21:38531355 C ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1793878 21:38531355 C CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1793878 21:38531355 C 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1793878 21:38531355 C ENSESTG00000029041 ENSESTT00000074108 Transcript intron_variant - - - - - - rs1793878 21:38531355 C ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1793878 21:38531355 C 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1793878 21:38531355 C ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1793878 21:38531355 C ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs1793879 21:38531406 C - ENSR00001051241 RegulatoryFeature regulatory_region_variant - - - - - - rs1793879 21:38531406 C ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1793879 21:38531406 C CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1793879 21:38531406 C 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1793879 21:38531406 C ENSESTG00000029041 ENSESTT00000074108 Transcript intron_variant - - - - - - rs1793879 21:38531406 C ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1793879 21:38531406 C 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1793879 21:38531406 C ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1793879 21:38531406 C ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs1793880 21:38531474 T - ENSR00001051241 RegulatoryFeature regulatory_region_variant - - - - - - rs1793880 21:38531474 T ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1793880 21:38531474 T CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1793880 21:38531474 T 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1793880 21:38531474 T ENSESTG00000029041 ENSESTT00000074108 Transcript intron_variant - - - - - - rs1793880 21:38531474 T ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1793880 21:38531474 T 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1793880 21:38531474 T ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1793880 21:38531474 T ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs1787365 21:38531921 A - ENSR00001051241 RegulatoryFeature regulatory_region_variant - - - - - - rs1787365 21:38531921 A ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1787365 21:38531921 A CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1787365 21:38531921 A 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1787365 21:38531921 A ENSESTG00000029041 ENSESTT00000074108 Transcript intron_variant - - - - - - rs1787365 21:38531921 A ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1787365 21:38531921 A 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1787365 21:38531921 A ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1787365 21:38531921 A ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs1783036 21:38535296 A ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1783036 21:38535296 A CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1783036 21:38535296 A 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1783036 21:38535296 A ENSESTG00000029041 ENSESTT00000074108 Transcript intron_variant - - - - - - rs1783036 21:38535296 A ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1783036 21:38535296 A 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1783036 21:38535296 A ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1783036 21:38535296 A ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs1793883 21:38535400 T ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1793883 21:38535400 T CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1793883 21:38535400 T 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1793883 21:38535400 T ENSESTG00000029041 ENSESTT00000074108 Transcript intron_variant - - - - - - rs1793883 21:38535400 T ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1793883 21:38535400 T 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1793883 21:38535400 T ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1793883 21:38535400 T ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs1783037 21:38541098 A ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1783037 21:38541098 A CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1783037 21:38541098 A 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1783037 21:38541098 A ENSESTG00000029041 ENSESTT00000074108 Transcript intron_variant - - - - - - rs1783037 21:38541098 A ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1783037 21:38541098 A 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1783037 21:38541098 A ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1783037 21:38541098 A ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs1783038 21:38541192 G ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1783038 21:38541192 G CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1783038 21:38541192 G 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1783038 21:38541192 G ENSESTG00000029041 ENSESTT00000074108 Transcript intron_variant - - - - - - rs1783038 21:38541192 G ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1783038 21:38541192 G 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1783038 21:38541192 G ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1783038 21:38541192 G ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs1793858 21:38541339 C ENSESTG00000029041 ENSESTT00000073832 Transcript intron_variant - - - - - - rs1793858 21:38541339 C CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs1793858 21:38541339 C 7267 NM_003316.3 Transcript intron_variant - - - - - - rs1793858 21:38541339 C ENSESTG00000029041 ENSESTT00000074108 Transcript intron_variant - - - - - - rs1793858 21:38541339 C ENSESTG00000029041 ENSESTT00000074036 Transcript intron_variant - - - - - - rs1793858 21:38541339 C 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs1793858 21:38541339 C ENSESTG00000029041 ENSESTT00000073824 Transcript intron_variant - - - - - - rs1793858 21:38541339 C ENSESTG00000029041 ENSESTT00000074048 Transcript intron_variant - - - - - - rs4817854 21:38551798 T CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs4817854 21:38551798 T 7267 NM_003316.3 Transcript intron_variant - - - - - - rs4817854 21:38551798 T 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs4817854 21:38551798 T ENSESTG00000029459 ENSESTT00000074222 Transcript upstream_gene_variant - - - - - - DISTANCE=3280 rs4817855 21:38552112 T CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs4817855 21:38552112 T 7267 NM_003316.3 Transcript intron_variant - - - - - - rs4817855 21:38552112 T 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs4817855 21:38552112 T ENSESTG00000029459 ENSESTT00000074222 Transcript upstream_gene_variant - - - - - - DISTANCE=2966 rs4817856 21:38557782 A CCDS13651.1 CCDS13651.1 Transcript intron_variant - - - - - - rs4817856 21:38557782 A 7267 NM_003316.3 Transcript intron_variant - - - - - - rs4817856 21:38557782 A 7267 NM_001001894.1 Transcript intron_variant - - - - - - rs4817856 21:38557782 A ENSESTG00000029459 ENSESTT00000074222 Transcript intron_variant - - - - - - rs9975083 21:38827296 G 1859 NM_101395.2 Transcript intron_variant - - - - - - rs9975083 21:38827296 G ENSESTG00000029572 ENSESTT00000074456 Transcript intron_variant - - - - - - rs9975083 21:38827296 G ENSESTG00000029572 ENSESTT00000074389 Transcript intron_variant - - - - - - rs9975083 21:38827296 G CCDS42926.1 CCDS42926.1 Transcript intron_variant - - - - - - rs9975083 21:38827296 G 1859 NM_130436.2 Transcript intron_variant - - - - - - rs9975083 21:38827296 G 1859 NM_130438.2 Transcript intron_variant - - - - - - rs9975083 21:38827296 G CCDS42925.1 CCDS42925.1 Transcript intron_variant - - - - - - rs9975083 21:38827296 G ENSESTG00000029740 ENSESTT00000074797 Transcript intron_variant - - - - - - rs9975083 21:38827296 G CCDS13654.1 CCDS13654.1 Transcript intron_variant - - - - - - rs9975083 21:38827296 G CCDS13653.1 CCDS13653.1 Transcript intron_variant - - - - - - rs9975083 21:38827296 G 1859 NM_001396.3 Transcript intron_variant - - - - - - rs4817866 21:38862376 A 1859 NM_101395.2 Transcript intron_variant - - - - - - rs4817866 21:38862376 A ENSESTG00000029572 ENSESTT00000074493 Transcript intron_variant - - - - - - rs4817866 21:38862376 A ENSESTG00000029572 ENSESTT00000074456 Transcript downstream_gene_variant - - - - - - DISTANCE=3573 rs4817866 21:38862376 A CCDS42926.1 CCDS42926.1 Transcript intron_variant - - - - - - rs4817866 21:38862376 A 1859 NM_130436.2 Transcript intron_variant - - - - - - rs4817866 21:38862376 A 1859 NM_130438.2 Transcript intron_variant - - - - - - rs4817866 21:38862376 A CCDS42925.1 CCDS42925.1 Transcript intron_variant - - - - - - rs4817866 21:38862376 A ENSESTG00000029740 ENSESTT00000074797 Transcript intron_variant - - - - - - rs4817866 21:38862376 A CCDS13654.1 CCDS13654.1 Transcript intron_variant - - - - - - rs4817866 21:38862376 A CCDS13653.1 CCDS13653.1 Transcript intron_variant - - - - - - rs4817866 21:38862376 A ENSESTG00000029572 ENSESTT00000074535 Transcript intron_variant - - - - - - rs4817866 21:38862376 A 1859 NM_001396.3 Transcript intron_variant - - - - - - rs976893 21:38986445 C - - - intergenic_variant - - - - - - rs857945 21:39014527 G ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs857945 21:39014527 G 3763 NM_002240.3 Transcript intron_variant - - - - - - rs857945 21:39014527 G CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs857944 21:39014688 G ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs857944 21:39014688 G 3763 NM_002240.3 Transcript intron_variant - - - - - - rs857944 21:39014688 G CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs857982 21:39026838 G ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs857982 21:39026838 G 3763 NM_002240.3 Transcript intron_variant - - - - - - rs857982 21:39026838 G CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs702861 21:39029053 G ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs702861 21:39029053 G 3763 NM_002240.3 Transcript intron_variant - - - - - - rs702861 21:39029053 G CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs1537103 21:39037719 A - ENSR00001566784 RegulatoryFeature regulatory_region_variant - - - - - - rs1537103 21:39037719 A ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs1537103 21:39037719 A 3763 NM_002240.3 Transcript intron_variant - - - - - - rs1537103 21:39037719 A CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs1709824 21:39051135 A ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs1709824 21:39051135 A 3763 NM_002240.3 Transcript intron_variant - - - - - - rs1709824 21:39051135 A CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs1709823 21:39052259 A ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs1709823 21:39052259 A 3763 NM_002240.3 Transcript intron_variant - - - - - - rs1709823 21:39052259 A CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs1709803 21:39056340 A ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs1709803 21:39056340 A 3763 NM_002240.3 Transcript intron_variant - - - - - - rs1709803 21:39056340 A CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs74440519 21:39079251 A ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs74440519 21:39079251 A 3763 NM_002240.3 Transcript intron_variant - - - - - - rs74440519 21:39079251 A CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs1612372 21:39079299 T ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs1612372 21:39079299 T 3763 NM_002240.3 Transcript intron_variant - - - - - - rs1612372 21:39079299 T CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs1787424 21:39079302 C ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs1787424 21:39079302 C 3763 NM_002240.3 Transcript intron_variant - - - - - - rs1787424 21:39079302 C CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs1709807 21:39079522 G ENSESTG00000029721 ENSESTT00000074779 Transcript intron_variant - - - - - - rs1709807 21:39079522 G 3763 NM_002240.3 Transcript intron_variant - - - - - - rs1709807 21:39079522 G CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs857961 21:39089582 G ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs857961 21:39089582 G ENSESTG00000029721 ENSESTT00000074779 Transcript upstream_gene_variant - - - - - - DISTANCE=2976 rs857961 21:39089582 G 3763 NM_002240.3 Transcript intron_variant - - - - - - rs857961 21:39089582 G CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs857961 21:39089582 G ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs858029 21:39102979 G ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs858029 21:39102979 G 3763 NM_002240.3 Transcript intron_variant - - - - - - rs858029 21:39102979 G CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs858029 21:39102979 G ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs857988 21:39117330 A - ENSR00000613648 RegulatoryFeature regulatory_region_variant - - - - - - rs857988 21:39117330 A ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs857988 21:39117330 A 3763 NM_002240.3 Transcript intron_variant - - - - - - rs857988 21:39117330 A CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs857988 21:39117330 A ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs857990 21:39125743 G ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs857990 21:39125743 G 3763 NM_002240.3 Transcript intron_variant - - - - - - rs857990 21:39125743 G CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs857990 21:39125743 G ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs9975118 21:39200089 T ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs9975118 21:39200089 T 3763 NM_002240.3 Transcript intron_variant - - - - - - rs9975118 21:39200089 T CCDS42927.1 CCDS42927.1 Transcript intron_variant - - - - - - rs9975118 21:39200089 T ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs6517440 21:39248613 A ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs6517440 21:39248613 A 3763 NM_002240.3 Transcript intron_variant - - - - - - rs6517440 21:39248613 A ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs9647174 21:39249156 A ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs9647174 21:39249156 A 3763 NM_002240.3 Transcript intron_variant - - - - - - rs9647174 21:39249156 A ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs4816586 21:39250250 A ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs4816586 21:39250250 A 3763 NM_002240.3 Transcript intron_variant - - - - - - rs4816586 21:39250250 A ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs6517441 21:39251304 C - ENSR00001566823 RegulatoryFeature regulatory_region_variant - - - - - - rs6517441 21:39251304 C ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs6517441 21:39251304 C 3763 NM_002240.3 Transcript intron_variant - - - - - - rs6517441 21:39251304 C ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs11088412 21:39255387 T ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs11088412 21:39255387 T 3763 NM_002240.3 Transcript intron_variant - - - - - - rs11088412 21:39255387 T ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs2226359 21:39268305 G ENSESTG00000029692 ENSESTT00000074741 Transcript intron_variant - - - - - - rs2226359 21:39268305 G 3763 NM_002240.3 Transcript intron_variant - - - - - - rs2226359 21:39268305 G ENSESTG00000029692 ENSESTT00000074716 Transcript intron_variant - - - - - - rs1005177 21:39300349 C - - - intergenic_variant - - - - - - rs2839973 21:39328350 C - - - intergenic_variant - - - - - - rs11702195 21:39433081 G CCDS33554.1 CCDS33554.1 Transcript intron_variant - - - - - - rs11702195 21:39433081 G 10281 NM_005867.2 Transcript intron_variant - - - - - - rs11702132 21:39433332 C CCDS33554.1 CCDS33554.1 Transcript intron_variant - - - - - - rs11702132 21:39433332 C 10281 NM_005867.2 Transcript intron_variant - - - - - - rs2850126 21:39436183 T CCDS33554.1 CCDS33554.1 Transcript intron_variant - - - - - - rs2850126 21:39436183 T 10281 NM_005867.2 Transcript intron_variant - - - - - - rs2848940 21:39442559 T CCDS33554.1 CCDS33554.1 Transcript intron_variant - - - - - - rs2848940 21:39442559 T 10281 NM_005867.2 Transcript intron_variant - - - - - - rs4816588 21:39478714 A CCDS33554.1 CCDS33554.1 Transcript intron_variant - - - - - - rs4816588 21:39478714 A 10281 NM_005867.2 Transcript intron_variant - - - - - - rs9981103 21:39533340 A 84677 NR_026838.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4735 rs9981103 21:39533340 A 84677 NR_026842.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4735 rs9981103 21:39533340 A ENSESTG00000027782 ENSESTT00000069951 Transcript intron_variant - - - - - - rs9981103 21:39533340 A ENSESTG00000027782 ENSESTT00000069960 Transcript intron_variant - - - - - - rs9981103 21:39533340 A 84677 NR_026841.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4735 rs9981103 21:39533340 A 84677 NR_026840.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4735 rs9981103 21:39533340 A ENSESTG00000027782 ENSESTT00000069943 Transcript intron_variant - - - - - - rs9981103 21:39533340 A 84677 NR_026839.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4735 rs9981103 21:39533340 A ENSESTG00000027767 ENSESTT00000069876 Transcript downstream_gene_variant - - - - - - DISTANCE=4248 rs4817917 21:39549046 G ENSESTG00000027782 ENSESTT00000069960 Transcript intron_variant - - - - - - rs4817917 21:39549046 G ENSESTG00000027782 ENSESTT00000069951 Transcript intron_variant - - - - - - rs4817917 21:39549046 G ENSESTG00000027782 ENSESTT00000069943 Transcript intron_variant - - - - - - rs2040233 21:39587934 G ENSESTG00000027782 ENSESTT00000069960 Transcript intron_variant - - - - - - rs2040233 21:39587934 G ENSESTG00000027782 ENSESTT00000069951 Transcript intron_variant - - - - - - rs2040233 21:39587934 G ENSESTG00000027782 ENSESTT00000069943 Transcript intron_variant - - - - - - rs2410012 21:39598539 C ENSESTG00000027782 ENSESTT00000069960 Transcript intron_variant - - - - - - rs2410012 21:39598539 C ENSESTG00000027782 ENSESTT00000069951 Transcript intron_variant - - - - - - rs2410012 21:39598539 C ENSESTG00000027782 ENSESTT00000069943 Transcript intron_variant - - - - - - rs4817934 21:39649698 G - ENSR00001566846 RegulatoryFeature regulatory_region_variant - - - - - - rs4817934 21:39649698 G ENSESTG00000027782 ENSESTT00000069960 Transcript intron_variant - - - - - - rs4817934 21:39649698 G 3772 NM_002243.3 Transcript intron_variant - - - - - - rs4817934 21:39649698 G 3772 NM_170736.1 Transcript intron_variant - - - - - - rs4817934 21:39649698 G 3772 NM_170737.1 Transcript intron_variant - - - - - - rs4817934 21:39649698 G ENSESTG00000027782 ENSESTT00000069951 Transcript intron_variant - - - - - - rs4817934 21:39649698 G ENSESTG00000027782 ENSESTT00000069943 Transcript intron_variant - - - - - - rs4817934 21:39649698 G ENSESTG00000027782 ENSESTT00000069972 Transcript intron_variant - - - - - - rs8132550 21:39656297 C ENSESTG00000027782 ENSESTT00000069960 Transcript intron_variant - - - - - - rs8132550 21:39656297 C 3772 NM_002243.3 Transcript intron_variant - - - - - - rs8132550 21:39656297 C 3772 NM_170736.1 Transcript intron_variant - - - - - - rs8132550 21:39656297 C 3772 NM_170737.1 Transcript intron_variant - - - - - - rs8132550 21:39656297 C ENSESTG00000027782 ENSESTT00000069951 Transcript intron_variant - - - - - - rs8132550 21:39656297 C ENSESTG00000027782 ENSESTT00000069943 Transcript intron_variant - - - - - - rs8132550 21:39656297 C ENSESTG00000027782 ENSESTT00000069972 Transcript intron_variant - - - - - - rs9284463 21:39739071 C 2078 NM_001243432.1 Transcript downstream_gene_variant - - - - - - DISTANCE=112 rs8130880 21:39743658 T 2078 NM_001243432.1 Transcript intron_variant - - - - - - rs8130880 21:39743658 T ENSESTG00000027840 ENSESTT00000070049 Transcript upstream_gene_variant - - - - - - DISTANCE=3750 rs2410031 21:39829391 A 2078 NM_001243429.1 Transcript intron_variant - - - - - - rs2410031 21:39829391 A ENSESTG00000027935 ENSESTT00000070393 Transcript intron_variant - - - - - - rs2410031 21:39829391 A ENSESTG00000027935 ENSESTT00000070323 Transcript intron_variant - - - - - - rs2410031 21:39829391 A CCDS46648.1 CCDS46648.1 Transcript intron_variant - - - - - - rs2410031 21:39829391 A 2078 NM_001243428.1 Transcript intron_variant - - - - - - rs2410031 21:39829391 A CCDS13658.1 CCDS13658.1 Transcript intron_variant - - - - - - rs2410031 21:39829391 A 2078 NM_182918.3 Transcript intron_variant - - - - - - rs2410031 21:39829391 A 2078 NM_001136154.1 Transcript intron_variant - - - - - - rs2410031 21:39829391 A 2078 NM_004449.4 Transcript intron_variant - - - - - - rs2410031 21:39829391 A 2078 NM_001243432.1 Transcript intron_variant - - - - - - rs2410031 21:39829391 A ENSESTG00000027935 ENSESTT00000070374 Transcript intron_variant - - - - - - rs2410031 21:39829391 A ENSESTG00000027935 ENSESTT00000070329 Transcript intron_variant - - - - - - rs2410031 21:39829391 A CCDS13657.1 CCDS13657.1 Transcript intron_variant - - - - - - rs2410031 21:39829391 A 2078 NM_001136155.1 Transcript intron_variant - - - - - - rs458835 21:40005348 C 2078 NM_001243432.1 Transcript intron_variant - - - - - - rs458835 21:40005348 C 2078 NM_004449.4 Transcript intron_variant - - - - - - rs458835 21:40005348 C 2078 NM_001136154.1 Transcript intron_variant - - - - - - rs458835 21:40005348 C ENSESTG00000027935 ENSESTT00000070323 Transcript intron_variant - - - - - - rs458835 21:40005348 C ENSESTG00000027935 ENSESTT00000070329 Transcript intron_variant - - - - - - rs458835 21:40005348 C 2078 NM_001243428.1 Transcript intron_variant - - - - - - rs2410047 21:40063471 G - ENSR00000613803 RegulatoryFeature regulatory_region_variant - - - - - - rs2410047 21:40063471 G - - - intergenic_variant - - - - - - rs1013840 21:40172414 C - ENSR00000613826 RegulatoryFeature regulatory_region_variant - - - - - - rs1013840 21:40172414 C 2114 NM_001256295.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4817 rs2142108 21:40301990 G - - - intergenic_variant - - - - - - rs9981985 21:40305996 C - - - intergenic_variant - - - - - - rs13048146 21:40309315 C - - - intergenic_variant - - - - - - rs76020318 21:40316205 C - - - intergenic_variant - - - - - - rs4817975 21:40334729 C - - - intergenic_variant - - - - - - rs10854392 21:40337189 G - ENSR00001051277 RegulatoryFeature regulatory_region_variant - - - - - - rs10854392 21:40337189 G - - - intergenic_variant - - - - - - rs8128400 21:40341846 C - - - intergenic_variant - - - - - - rs8131331 21:40355053 G - - - intergenic_variant - - - - - - rs2410076 21:40364037 G - - - intergenic_variant - - - - - - rs9983089 21:40373347 C - - - intergenic_variant - - - - - - rs7278809 21:40373784 C - - - intergenic_variant - - - - - - rs9305661 21:40381769 G - - - intergenic_variant - - - - - - rs7275942 21:40383903 C - - - intergenic_variant - - - - - - rs914154 21:40417472 G - - - intergenic_variant - - - - - - rs418814 21:40489882 C - - - intergenic_variant - - - - - - rs763892 21:40496346 G - - - intergenic_variant - - - - - - rs9984161 21:40553491 G ENSESTG00000017725 ENSESTT00000044739 Transcript intron_variant - - - - - - rs9984161 21:40553491 G 8624 NM_003720.3 Transcript intron_variant - - - - - - rs9984161 21:40553491 G 8624 NM_203433.2 Transcript intron_variant - - - - - - rs9984161 21:40553491 G 54014 NM_033656.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3913 rs9984161 21:40553491 G CCDS13661.1 CCDS13661.1 Transcript intron_variant - - - - - - rs9984161 21:40553491 G 8624 NM_001261824.1 Transcript intron_variant - - - - - - rs9984161 21:40553491 G 8624 NR_049728.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9984161 21:40553491 G 54014 NM_018963.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3913 rs9984161 21:40553491 G ENSESTG00000017725 ENSESTT00000044760 Transcript upstream_gene_variant - - - - - - DISTANCE=1127 rs9984161 21:40553491 G CCDS13660.1 CCDS13660.1 Transcript intron_variant - - - - - - rs9984161 21:40553491 G ENSESTG00000017725 ENSESTT00000044717 Transcript intron_variant - - - - - - rs2065312 21:40610274 T - ENSR00001566969 RegulatoryFeature regulatory_region_variant - - - - - - rs2065312 21:40610274 T CCDS13662.1 CCDS13662.1 Transcript intron_variant - - - - - - rs2065312 21:40610274 T CCDS13663.1 CCDS13663.1 Transcript intron_variant - - - - - - rs2065312 21:40610274 T 54014 NM_018963.4 Transcript intron_variant - - - - - - rs2065312 21:40610274 T ENSESTG00000017637 ENSESTT00000044518 Transcript intron_variant - - - - - - rs2065312 21:40610274 T 54014 NM_033656.3 Transcript intron_variant - - - - - - rs7275629 21:40645980 C CCDS13662.1 CCDS13662.1 Transcript intron_variant - - - - - - rs7275629 21:40645980 C CCDS13663.1 CCDS13663.1 Transcript intron_variant - - - - - - rs7275629 21:40645980 C 54014 NM_018963.4 Transcript intron_variant - - - - - - rs7275629 21:40645980 C 54014 NM_033656.3 Transcript intron_variant - - - - - - rs987375 21:41038646 A 10317 NM_006057.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3831 rs987375 21:41038646 A ENSESTG00000017422 ENSESTT00000043810 Transcript downstream_gene_variant - - - - - - DISTANCE=4567 rs987375 21:41038646 A 10317 NM_033172.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3831 rs987375 21:41038646 A 10317 NM_033170.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3831 rs987375 21:41038646 A 10317 NM_033171.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3831 rs987375 21:41038646 A ENSESTG00000017409 ENSESTT00000043786 Transcript intron_variant - - - - - - rs4818073 21:41069784 C ENSESTG00000017409 ENSESTT00000043786 Transcript intron_variant - - - - - - rs9979209 21:41317515 C - - - intergenic_variant - - - - - - rs7282561 21:41318069 C - - - intergenic_variant - - - - - - rs760123 21:41806774 C 1826 NM_001389.3 Transcript intron_variant - - - - - - rs760123 21:41806774 C CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs8129410 21:41869515 A 1826 NM_001389.3 Transcript intron_variant - - - - - - rs8129410 21:41869515 A CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs1571723 21:41894039 A 1826 NM_001389.3 Transcript intron_variant - - - - - - rs1571723 21:41894039 A CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs11702038 21:41907666 A 1826 NM_001389.3 Transcript intron_variant - - - - - - rs11702038 21:41907666 A CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs63309160 21:41918411 C 1826 NM_001389.3 Transcript intron_variant - - - - - - rs63309160 21:41918411 C CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs423555 21:41975430 G 1826 NM_001389.3 Transcript intron_variant - - - - - - rs423555 21:41975430 G CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs365533 21:42002600 G 100874326 NR_046774.1 Transcript non_coding_exon_variant,nc_transcript_variant 94 - - - - - rs365533 21:42002600 G ENSESTG00000015188 ENSESTT00000038027 Transcript 5_prime_UTR_variant 97 - - - - - rs365533 21:42002600 G ENSESTG00000015188 ENSESTT00000038019 Transcript 5_prime_UTR_variant 99 - - - - - rs365533 21:42002600 G 1826 NM_001389.3 Transcript intron_variant - - - - - - rs365533 21:42002600 G CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs7275475 21:42055420 G 1826 NM_001389.3 Transcript intron_variant - - - - - - rs7275475 21:42055420 G CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs9978898 21:42065361 C 1826 NM_001389.3 Transcript intron_variant - - - - - - rs9978898 21:42065361 C ENSESTG00000015179 ENSESTT00000038003 Transcript intron_variant - - - - - - rs9978898 21:42065361 C CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs9980887 21:42065803 G 1826 NM_001389.3 Transcript intron_variant - - - - - - rs9980887 21:42065803 G ENSESTG00000015179 ENSESTT00000038003 Transcript intron_variant - - - - - - rs9980887 21:42065803 G CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs4818165 21:42067041 C 1826 NM_001389.3 Transcript intron_variant - - - - - - rs4818165 21:42067041 C ENSESTG00000015179 ENSESTT00000038003 Transcript intron_variant - - - - - - rs4818165 21:42067041 C CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs1041442 21:42121710 C 1826 NM_001389.3 Transcript intron_variant - - - - - - rs1041442 21:42121710 C ENSESTG00000015179 ENSESTT00000038003 Transcript intron_variant - - - - - - rs1041442 21:42121710 C CCDS42929.1 CCDS42929.1 Transcript intron_variant - - - - - - rs8130635 21:42225387 C - - - intergenic_variant - - - - - - rs2091874 21:42247436 A - - - intergenic_variant - - - - - - rs7279837 21:42454582 T - - - intergenic_variant - - - - - - rs944415 21:42461549 G - - - intergenic_variant - - - - - - rs944417 21:42461665 A - - - intergenic_variant - - - - - - rs4818214 21:42526541 G ENSESTG00000003112 ENSESTT00000007738 Transcript intron_variant - - - - - - rs414382 21:42698046 C CCDS42930.1 CCDS42930.1 Transcript intron_variant - - - - - - rs414382 21:42698046 C 54097 NM_058186.3 Transcript intron_variant - - - - - - rs414382 21:42698046 C CCDS13671.1 CCDS13671.1 Transcript intron_variant - - - - - - rs414382 21:42698046 C 54097 NM_206964.1 Transcript intron_variant - - - - - - rs414382 21:42698046 C ENSESTG00000002969 ENSESTT00000007395 Transcript intron_variant - - - - - - rs414382 21:42698046 C ENSESTG00000002969 ENSESTT00000007390 Transcript intron_variant - - - - - - rs462161 21:42775555 G ENSESTG00000003005 ENSESTT00000007471 Transcript intron_variant - - - - - - rs462161 21:42775555 G 4600 NM_002463.1 Transcript intron_variant - - - - - - rs462161 21:42775555 G CCDS13672.1 CCDS13672.1 Transcript intron_variant - - - - - - rs455598 21:42819130 A ENSESTG00000003014 ENSESTT00000007603 Transcript intron_variant - - - - - - rs455598 21:42819130 A CCDS13673.1 CCDS13673.1 Transcript intron_variant - - - - - - rs455598 21:42819130 A 4599 NM_001178046.1 Transcript intron_variant - - - - - - rs455598 21:42819130 A ENSESTG00000003014 ENSESTT00000007600 Transcript intron_variant - - - - - - rs455598 21:42819130 A ENSESTG00000003014 ENSESTT00000007592 Transcript intron_variant - - - - - - rs455598 21:42819130 A 4599 NM_002462.3 Transcript intron_variant - - - - - - rs455598 21:42819130 A 4599 NM_001144925.1 Transcript intron_variant - - - - - - rs455598 21:42819130 A ENSESTG00000003014 ENSESTT00000007605 Transcript intron_variant - - - - - - rs381179 21:42857642 C ENSESTG00000003089 ENSESTT00000007683 Transcript intron_variant - - - - - - rs381179 21:42857642 C ENSESTG00000003089 ENSESTT00000007698 Transcript intron_variant - - - - - - rs381179 21:42857642 C ENSESTG00000003089 ENSESTT00000007708 Transcript intron_variant - - - - - - rs381179 21:42857642 C CCDS33564.1 CCDS33564.1 Transcript intron_variant - - - - - - rs381179 21:42857642 C 7113 NM_001135099.1 Transcript intron_variant - - - - - - rs381179 21:42857642 C CCDS54486.1 CCDS54486.1 Transcript intron_variant - - - - - - rs381179 21:42857642 C ENSESTG00000003089 ENSESTT00000007693 Transcript intron_variant - - - - - - rs381179 21:42857642 C ENSESTG00000003089 ENSESTT00000007705 Transcript intron_variant - - - - - - rs381179 21:42857642 C ENSESTG00000003089 ENSESTT00000007706 Transcript intron_variant - - - - - - rs381179 21:42857642 C ENSESTG00000003089 ENSESTT00000007692 Transcript intron_variant - - - - - - rs381179 21:42857642 C 7113 NM_005656.3 Transcript intron_variant - - - - - - rs28532664 21:42953162 C - ENSR00000614107 RegulatoryFeature regulatory_region_variant - - - - - - rs28532664 21:42953162 C - - - intergenic_variant - - - - - - rs4919943 21:43182229 C - ENSR00001567105 RegulatoryFeature regulatory_region_variant - - - - - - rs4919943 21:43182229 C 54101 NM_020639.2 Transcript intron_variant - - - - - - rs4919943 21:43182229 C ENSESTG00000003071 ENSESTT00000007653 Transcript intron_variant - - - - - - rs4919943 21:43182229 C ENSESTG00000003071 ENSESTT00000007657 Transcript intron_variant - - - - - - rs4919943 21:43182229 C CCDS13675.1 CCDS13675.1 Transcript intron_variant - - - - - - rs28406845 21:43237846 C - ENSR00001050908 RegulatoryFeature regulatory_region_variant - - - - - - rs28406845 21:43237846 C ENSESTG00000012429 ENSESTT00000031160 Transcript intron_variant - - - - - - rs28406845 21:43237846 C ENSESTG00000012429 ENSESTT00000031155 Transcript intron_variant - - - - - - rs28406845 21:43237846 C CCDS42932.1 CCDS42932.1 Transcript intron_variant - - - - - - rs28406845 21:43237846 C 63977 NM_022115.3 Transcript intron_variant - - - - - - rs28406845 21:43237846 C ENSESTG00000012429 ENSESTT00000031157 Transcript downstream_gene_variant - - - - - - DISTANCE=4411 rs28406845 21:43237846 C ENSESTG00000012429 ENSESTT00000031151 Transcript intron_variant - - - - - - rs28406845 21:43237846 C CCDS13676.1 CCDS13676.1 Transcript intron_variant - - - - - - rs28406845 21:43237846 C 63977 NM_001040424.1 Transcript intron_variant - - - - - - rs28406845 21:43237846 C ENSESTG00000012429 ENSESTT00000031152 Transcript downstream_gene_variant - - - - - - DISTANCE=4411 rs28404992 21:43238036 A ENSESTG00000012429 ENSESTT00000031160 Transcript intron_variant - - - - - - rs28404992 21:43238036 A ENSESTG00000012429 ENSESTT00000031155 Transcript intron_variant - - - - - - rs28404992 21:43238036 A CCDS42932.1 CCDS42932.1 Transcript intron_variant - - - - - - rs28404992 21:43238036 A 63977 NM_022115.3 Transcript intron_variant - - - - - - rs28404992 21:43238036 A ENSESTG00000012429 ENSESTT00000031157 Transcript downstream_gene_variant - - - - - - DISTANCE=4221 rs28404992 21:43238036 A ENSESTG00000012429 ENSESTT00000031151 Transcript intron_variant - - - - - - rs28404992 21:43238036 A CCDS13676.1 CCDS13676.1 Transcript intron_variant - - - - - - rs28404992 21:43238036 A 63977 NM_001040424.1 Transcript intron_variant - - - - - - rs28404992 21:43238036 A ENSESTG00000012429 ENSESTT00000031152 Transcript downstream_gene_variant - - - - - - DISTANCE=4221 rs220221 21:43446094 C 150142 NR_027273.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1034 rs220221 21:43446094 C ENSESTG00000012147 ENSESTT00000030395 Transcript downstream_gene_variant - - - - - - DISTANCE=1034 rs150789 21:43460129 A - ENSR00001567124 RegulatoryFeature regulatory_region_variant - - - - - - rs150789 21:43460129 A - - - intergenic_variant - - - - - - rs221961 21:43603677 G - - - intergenic_variant - - - - - - rs221949 21:43627315 T 9619 NM_207627.1 Transcript intron_variant - - - - - - rs221949 21:43627315 T CCDS42937.1 CCDS42937.1 Transcript intron_variant - - - - - - rs221949 21:43627315 T 9619 NM_207628.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C ENSESTG00000012181 ENSESTT00000030513 Transcript downstream_gene_variant - - - - - - DISTANCE=476 rs498754 21:43712131 C 9619 NM_004915.3 Transcript intron_variant - - - - - - rs498754 21:43712131 C 9619 NM_207627.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C CCDS13683.1 CCDS13683.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C ENSESTG00000012181 ENSESTT00000030502 Transcript downstream_gene_variant - - - - - - DISTANCE=861 rs498754 21:43712131 C ENSESTG00000012181 ENSESTT00000030516 Transcript downstream_gene_variant - - - - - - DISTANCE=502 rs498754 21:43712131 C 9619 NM_016818.2 Transcript intron_variant - - - - - - rs498754 21:43712131 C CCDS42938.1 CCDS42938.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C CCDS13682.1 CCDS13682.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C ENSESTG00000012181 ENSESTT00000030505 Transcript downstream_gene_variant - - - - - - DISTANCE=861 rs498754 21:43712131 C ENSESTG00000012181 ENSESTT00000030493 Transcript downstream_gene_variant - - - - - - DISTANCE=861 rs498754 21:43712131 C 9619 NM_207174.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C 9619 NM_207628.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C ENSESTG00000012181 ENSESTT00000030494 Transcript downstream_gene_variant - - - - - - DISTANCE=861 rs498754 21:43712131 C CCDS42937.1 CCDS42937.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C ENSESTG00000012181 ENSESTT00000030500 Transcript intron_variant - - - - - - rs498754 21:43712131 C CCDS13681.1 CCDS13681.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C 9619 NM_207629.1 Transcript intron_variant - - - - - - rs498754 21:43712131 C ENSESTG00000012181 ENSESTT00000030485 Transcript intron_variant - - - - - - rs225425 21:43748689 A - - - intergenic_variant - - - - - - rs225312 21:43812161 T CCDS42939.1 CCDS42939.1 Transcript intron_variant - - - - - - rs225312 21:43812161 T ENSESTG00000012320 ENSESTT00000030930 Transcript upstream_gene_variant - - - - - - DISTANCE=2944 rs225312 21:43812161 T CCDS58790.1 CCDS58790.1 Transcript intron_variant - - - - - - rs225312 21:43812161 T ENSESTG00000012320 ENSESTT00000030914 Transcript upstream_gene_variant - - - - - - DISTANCE=2014 rs225312 21:43812161 T 64699 NM_032405.1 Transcript intron_variant - - - - - - rs225312 21:43812161 T 64699 NR_046020.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs225312 21:43812161 T 64699 NM_032404.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2903 rs225312 21:43812161 T ENSESTG00000012320 ENSESTT00000030928 Transcript upstream_gene_variant - - - - - - DISTANCE=2944 rs225312 21:43812161 T 64699 NM_024022.2 Transcript intron_variant - - - - - - rs225312 21:43812161 T ENSESTG00000012320 ENSESTT00000030891 Transcript intron_variant - - - - - - rs225312 21:43812161 T CCDS13686.1 CCDS13686.1 Transcript intron_variant - - - - - - rs225312 21:43812161 T ENSESTG00000012320 ENSESTT00000030897 Transcript intron_variant - - - - - - rs225312 21:43812161 T ENSESTG00000012320 ENSESTT00000030877 Transcript intron_variant - - - - - - rs225312 21:43812161 T 64699 NM_001256317.1 Transcript intron_variant - - - - - - rs1153362 21:43902956 C CCDS13688.1 CCDS13688.1 Transcript intron_variant - - - - - - rs1153362 21:43902956 C ENSESTG00000012301 ENSESTT00000030864 Transcript intron_variant - - - - - - rs1153362 21:43902956 C 89765 NM_080860.2 Transcript intron_variant - - - - - - rs1153362 21:43902956 C ENSESTG00000012301 ENSESTT00000030865 Transcript downstream_gene_variant - - - - - - DISTANCE=3346 rs1153363 21:43904965 G CCDS13688.1 CCDS13688.1 Transcript intron_variant - - - - - - rs1153363 21:43904965 G ENSESTG00000012301 ENSESTT00000030864 Transcript intron_variant - - - - - - rs1153363 21:43904965 G 89765 NM_080860.2 Transcript intron_variant - - - - - - rs1153363 21:43904965 G ENSESTG00000012301 ENSESTT00000030865 Transcript downstream_gene_variant - - - - - - DISTANCE=1337 rs4920115 21:43931876 C 54020 NM_018964.3 Transcript intron_variant - - - - - - rs4920115 21:43931876 C ENSESTG00000012214 ENSESTT00000030577 Transcript downstream_gene_variant - - - - - - DISTANCE=2382 rs4920115 21:43931876 C ENSESTG00000012214 ENSESTT00000030573 Transcript intron_variant - - - - - - rs4920115 21:43931876 C ENSESTG00000012214 ENSESTT00000030628 Transcript upstream_gene_variant - - - - - - DISTANCE=2397 rs4920115 21:43931876 C ENSESTG00000012214 ENSESTT00000030590 Transcript upstream_gene_variant - - - - - - DISTANCE=2128 rs4920115 21:43931876 C ENSESTG00000012214 ENSESTT00000030588 Transcript upstream_gene_variant - - - - - - DISTANCE=2108 rs4920115 21:43931876 C ENSESTG00000012214 ENSESTT00000030620 Transcript upstream_gene_variant - - - - - - DISTANCE=2397 rs2399146 21:43949967 G 54020 NM_018964.3 Transcript intron_variant - - - - - - rs2399146 21:43949967 G ENSESTG00000012214 ENSESTT00000030573 Transcript downstream_gene_variant - - - - - - DISTANCE=3999 rs2399146 21:43949967 G ENSESTG00000012214 ENSESTT00000030628 Transcript intron_variant - - - - - - rs2399146 21:43949967 G CCDS13689.1 CCDS13689.1 Transcript intron_variant - - - - - - rs2399146 21:43949967 G ENSESTG00000012214 ENSESTT00000030590 Transcript downstream_gene_variant - - - - - - DISTANCE=3819 rs2399146 21:43949967 G ENSESTG00000012214 ENSESTT00000030588 Transcript intron_variant - - - - - - rs2399146 21:43949967 G ENSESTG00000012214 ENSESTT00000030620 Transcript intron_variant - - - - - - rs2399146 21:43949967 G ENSESTG00000012214 ENSESTT00000030635 Transcript downstream_gene_variant - - - - - - DISTANCE=3345 rs228064 21:43959979 G - ENSR00000684394 RegulatoryFeature regulatory_region_variant - - - - - - rs228064 21:43959979 G CCDS13689.1 CCDS13689.1 Transcript intron_variant - - - - - - rs228064 21:43959979 G 54020 NM_018964.3 Transcript intron_variant - - - - - - rs228064 21:43959979 G ENSESTG00000012214 ENSESTT00000030639 Transcript intron_variant - - - - - - rs228064 21:43959979 G ENSESTG00000012214 ENSESTT00000030628 Transcript intron_variant - - - - - - rs228064 21:43959979 G ENSESTG00000012214 ENSESTT00000030588 Transcript intron_variant - - - - - - rs228064 21:43959979 G ENSESTG00000012214 ENSESTT00000030638 Transcript intron_variant - - - - - - rs228064 21:43959979 G ENSESTG00000012214 ENSESTT00000030620 Transcript intron_variant - - - - - - rs228065 21:43960009 G - ENSR00000684394 RegulatoryFeature regulatory_region_variant - - - - - - rs228065 21:43960009 G CCDS13689.1 CCDS13689.1 Transcript intron_variant - - - - - - rs228065 21:43960009 G 54020 NM_018964.3 Transcript intron_variant - - - - - - rs228065 21:43960009 G ENSESTG00000012214 ENSESTT00000030639 Transcript intron_variant - - - - - - rs228065 21:43960009 G ENSESTG00000012214 ENSESTT00000030628 Transcript intron_variant - - - - - - rs228065 21:43960009 G ENSESTG00000012214 ENSESTT00000030588 Transcript intron_variant - - - - - - rs228065 21:43960009 G ENSESTG00000012214 ENSESTT00000030638 Transcript intron_variant - - - - - - rs228065 21:43960009 G ENSESTG00000012214 ENSESTT00000030620 Transcript intron_variant - - - - - - rs228066 21:43960063 G - ENSR00000684394 RegulatoryFeature regulatory_region_variant - - - - - - rs228066 21:43960063 G CCDS13689.1 CCDS13689.1 Transcript intron_variant - - - - - - rs228066 21:43960063 G 54020 NM_018964.3 Transcript intron_variant - - - - - - rs228066 21:43960063 G ENSESTG00000012214 ENSESTT00000030639 Transcript intron_variant - - - - - - rs228066 21:43960063 G ENSESTG00000012214 ENSESTT00000030628 Transcript intron_variant - - - - - - rs228066 21:43960063 G ENSESTG00000012214 ENSESTT00000030588 Transcript intron_variant - - - - - - rs228066 21:43960063 G ENSESTG00000012214 ENSESTT00000030638 Transcript intron_variant - - - - - - rs228066 21:43960063 G ENSESTG00000012214 ENSESTT00000030620 Transcript intron_variant - - - - - - rs368969 21:44061555 C - ENSR00001567165 RegulatoryFeature regulatory_region_variant - - - - - - rs368969 21:44061555 C - - - intergenic_variant - - - - - - rs55765736 21:44632556 A - - - intergenic_variant - - - - - - rs636957 21:44731687 C - - - intergenic_variant - - - - - - rs635360 21:44751824 A - ENSR00000614443 RegulatoryFeature regulatory_region_variant - - - - - - rs635360 21:44751824 A - - - intergenic_variant - - - - - - rs514626 21:44819909 C - ENSR00000614463 RegulatoryFeature regulatory_region_variant - - - - - - rs514626 21:44819909 C - - - intergenic_variant - - - - - - rs229354 21:44922228 C - ENSR00001567230 RegulatoryFeature regulatory_region_variant - - - - - - rs229354 21:44922228 C - - - intergenic_variant - - - - - - rs229358 21:44965848 A CCDS13697.1 CCDS13697.1 Transcript intron_variant - - - - - - rs229358 21:44965848 A 11077 NM_007031.1 Transcript intron_variant - - - - - - rs229358 21:44965848 A ENSESTG00000022067 ENSESTT00000055735 Transcript intron_variant - - - - - - rs7282274 21:45156674 G ENSESTG00000022055 ENSESTT00000055539 Transcript upstream_gene_variant - - - - - - DISTANCE=4463 rs7282274 21:45156674 G ENSESTG00000021905 ENSESTT00000055465 Transcript upstream_gene_variant - - - - - - DISTANCE=4695 rs7282274 21:45156674 G ENSESTG00000021905 ENSESTT00000055450 Transcript upstream_gene_variant - - - - - - DISTANCE=4217 rs7282274 21:45156674 G ENSESTG00000021905 ENSESTT00000055404 Transcript intron_variant - - - - - - rs7282274 21:45156674 G CCDS13699.1 CCDS13699.1 Transcript intron_variant - - - - - - rs7282274 21:45156674 G ENSESTG00000021905 ENSESTT00000055396 Transcript intron_variant - - - - - - rs7282274 21:45156674 G 8566 NM_003681.4 Transcript intron_variant - - - - - - rs7282274 21:45156674 G ENSESTG00000021905 ENSESTT00000055388 Transcript intron_variant - - - - - - rs7282274 21:45156674 G ENSESTG00000021905 ENSESTT00000055426 Transcript downstream_gene_variant - - - - - - DISTANCE=2670 rs7282274 21:45156674 G ENSESTG00000021905 ENSESTT00000055373 Transcript intron_variant - - - - - - rs2329576 21:45220787 G ENSESTG00000015970 ENSESTT00000040143 Transcript downstream_gene_variant - - - - - - DISTANCE=226 rs2329576 21:45220787 G ENSESTG00000015970 ENSESTT00000040133 Transcript intron_variant - - - - - - rs2329576 21:45220787 G ENSESTG00000015970 ENSESTT00000040124 Transcript intron_variant - - - - - - rs2329576 21:45220787 G 284837 NR_026961.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4852 rs2329576 21:45220787 G CCDS42951.1 CCDS42951.1 Transcript intron_variant - - - - - - rs2329576 21:45220787 G 8568 NM_003683.5 Transcript intron_variant - - - - - - rs420826 21:45339066 G ENSESTG00000015921 ENSESTT00000040009 Transcript intron_variant - - - - - - rs420826 21:45339066 G ENSESTG00000015921 ENSESTT00000039966 Transcript intron_variant - - - - - - rs420826 21:45339066 G ENSESTG00000015921 ENSESTT00000039951 Transcript intron_variant - - - - - - rs420826 21:45339066 G ENSESTG00000015921 ENSESTT00000039946 Transcript intron_variant - - - - - - rs420826 21:45339066 G 56894 NM_020132.4 Transcript intron_variant - - - - - - rs2009783 21:45456648 A 7109 NM_003274.4 Transcript intron_variant - - - - - - rs2009783 21:45456648 A ENSESTG00000016041 ENSESTT00000040247 Transcript intron_variant - - - - - - rs2009783 21:45456648 A CCDS13704.1 CCDS13704.1 Transcript intron_variant - - - - - - rs2009783 21:45456648 A ENSESTG00000016041 ENSESTT00000040257 Transcript upstream_gene_variant - - - - - - DISTANCE=930 rs2009783 21:45456648 A ENSESTG00000016041 ENSESTT00000040254 Transcript intron_variant - - - - - - rs6518346 21:45491168 G 7109 NM_003274.4 Transcript intron_variant - - - - - - rs6518346 21:45491168 G ENSESTG00000016041 ENSESTT00000040247 Transcript intron_variant - - - - - - rs6518346 21:45491168 G CCDS13704.1 CCDS13704.1 Transcript intron_variant - - - - - - rs6518346 21:45491168 G ENSESTG00000016041 ENSESTT00000040257 Transcript intron_variant - - - - - - rs6518346 21:45491168 G ENSESTG00000016041 ENSESTT00000040265 Transcript upstream_gene_variant - - - - - - DISTANCE=3033 rs7280711 21:45512380 C ENSESTG00000016078 ENSESTT00000040329 Transcript intron_variant - - - - - - rs7280711 21:45512380 C ENSESTG00000016068 ENSESTT00000040281 Transcript downstream_gene_variant - - - - - - DISTANCE=4568 rs7280711 21:45512380 C 7109 NM_003274.4 Transcript intron_variant - - - - - - rs7280711 21:45512380 C ENSESTG00000016078 ENSESTT00000040326 Transcript intron_variant - - - - - - rs7280711 21:45512380 C ENSESTG00000016078 ENSESTT00000040332 Transcript intron_variant - - - - - - rs7280711 21:45512380 C CCDS13704.1 CCDS13704.1 Transcript intron_variant - - - - - - rs7282614 21:45512453 T ENSESTG00000016078 ENSESTT00000040329 Transcript intron_variant - - - - - - rs7282614 21:45512453 T ENSESTG00000016068 ENSESTT00000040281 Transcript downstream_gene_variant - - - - - - DISTANCE=4641 rs7282614 21:45512453 T 7109 NM_003274.4 Transcript intron_variant - - - - - - rs7282614 21:45512453 T ENSESTG00000016078 ENSESTT00000040326 Transcript intron_variant - - - - - - rs7282614 21:45512453 T ENSESTG00000016078 ENSESTT00000040332 Transcript intron_variant - - - - - - rs7282614 21:45512453 T CCDS13704.1 CCDS13704.1 Transcript intron_variant - - - - - - rs4819371 21:45514168 T ENSESTG00000016078 ENSESTT00000040329 Transcript intron_variant - - - - - - rs4819371 21:45514168 T 7109 NM_003274.4 Transcript intron_variant - - - - - - rs4819371 21:45514168 T ENSESTG00000016078 ENSESTT00000040326 Transcript intron_variant - - - - - - rs4819371 21:45514168 T ENSESTG00000016078 ENSESTT00000040332 Transcript intron_variant - - - - - - rs4819371 21:45514168 T CCDS13704.1 CCDS13704.1 Transcript intron_variant - - - - - - rs4818879 21:45514188 G ENSESTG00000016078 ENSESTT00000040329 Transcript intron_variant - - - - - - rs4818879 21:45514188 G 7109 NM_003274.4 Transcript intron_variant - - - - - - rs4818879 21:45514188 G ENSESTG00000016078 ENSESTT00000040326 Transcript intron_variant - - - - - - rs4818879 21:45514188 G ENSESTG00000016078 ENSESTT00000040332 Transcript intron_variant - - - - - - rs4818879 21:45514188 G CCDS13704.1 CCDS13704.1 Transcript intron_variant - - - - - - rs7277128 21:45520216 C ENSESTG00000016078 ENSESTT00000040329 Transcript downstream_gene_variant - - - - - - DISTANCE=3631 rs7277128 21:45520216 C 7109 NM_003274.4 Transcript intron_variant - - - - - - rs7277128 21:45520216 C ENSESTG00000016078 ENSESTT00000040326 Transcript intron_variant - - - - - - rs7277128 21:45520216 C ENSESTG00000016078 ENSESTT00000040332 Transcript intron_variant - - - - - - rs7277128 21:45520216 C ENSESTG00000016078 ENSESTT00000040335 Transcript upstream_gene_variant - - - - - - DISTANCE=2441 rs7277128 21:45520216 C CCDS13704.1 CCDS13704.1 Transcript intron_variant - - - - - - rs9637178 21:45520223 G ENSESTG00000016078 ENSESTT00000040329 Transcript downstream_gene_variant - - - - - - DISTANCE=3638 rs9637178 21:45520223 G 7109 NM_003274.4 Transcript intron_variant - - - - - - rs9637178 21:45520223 G ENSESTG00000016078 ENSESTT00000040326 Transcript intron_variant - - - - - - rs9637178 21:45520223 G ENSESTG00000016078 ENSESTT00000040332 Transcript intron_variant - - - - - - rs9637178 21:45520223 G ENSESTG00000016078 ENSESTT00000040335 Transcript upstream_gene_variant - - - - - - DISTANCE=2434 rs9637178 21:45520223 G CCDS13704.1 CCDS13704.1 Transcript intron_variant - - - - - - rs2776369 21:45534807 G ENSESTG00000016095 ENSESTT00000040446 Transcript intron_variant - - - - - - rs2776369 21:45534807 G 5822 NM_005049.2 Transcript intron_variant - - - - - - rs2776369 21:45534807 G CCDS33579.1 CCDS33579.1 Transcript intron_variant - - - - - - rs2776369 21:45534807 G ENSESTG00000016095 ENSESTT00000040411 Transcript intron_variant - - - - - - rs2776369 21:45534807 G ENSESTG00000016135 ENSESTT00000040599 Transcript upstream_gene_variant - - - - - - DISTANCE=917 rs9982286 21:45569229 G ENSESTG00000016199 ENSESTT00000040710 Transcript downstream_gene_variant - - - - - - DISTANCE=4190 rs9982286 21:45569229 G CCDS33581.1 CCDS33581.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4398 rs9982286 21:45569229 G ENSESTG00000016199 ENSESTT00000040707 Transcript downstream_gene_variant - - - - - - DISTANCE=3636 rs9982286 21:45569229 G ENSESTG00000016762 ENSESTT00000042066 Transcript intron_variant - - - - - - rs9982286 21:45569229 G 8209 NM_198155.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3624 rs9982286 21:45569229 G ENSESTG00000016199 ENSESTT00000040732 Transcript downstream_gene_variant - - - - - - DISTANCE=3636 rs9982286 21:45569229 G CCDS33580.1 CCDS33580.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4398 rs9982286 21:45569229 G 8209 NM_004649.6 Transcript downstream_gene_variant - - - - - - DISTANCE=3624 rs9975536 21:45582483 G ENSESTG00000016762 ENSESTT00000042066 Transcript intron_variant - - - - - - rs410586 21:45590673 C ENSESTG00000016762 ENSESTT00000042066 Transcript intron_variant - - - - - - rs412610 21:45591475 C - ENSR00000186151 RegulatoryFeature regulatory_region_variant - - - - - - rs412610 21:45591475 C ENSESTG00000016762 ENSESTT00000042066 Transcript intron_variant - - - - - - rs413328 21:45593242 G - ENSR00000614633 RegulatoryFeature regulatory_region_variant - - - - - - rs413328 21:45593242 G ENSESTG00000016762 ENSESTT00000042066 Transcript intron_variant - - - - - - rs2156429 21:45614375 C - ENSR00001567305 RegulatoryFeature regulatory_region_variant - - - - - - rs2156429 21:45614375 C ENSESTG00000016762 ENSESTT00000042066 Transcript intron_variant - - - - - - rs4818717 21:45782035 T CCDS13710.1 CCDS13710.1 Transcript intron_variant - - - - - - rs4818717 21:45782035 T 7226 NM_003307.3 Transcript intron_variant - - - - - - rs4818717 21:45782035 T ENSESTG00000016463 ENSESTT00000041288 Transcript intron_variant - - - - - - rs4818717 21:45782035 T 7226 NR_038257.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7280680 21:45786368 G CCDS13710.1 CCDS13710.1 Transcript intron_variant - - - - - - rs7280680 21:45786368 G 7226 NM_003307.3 Transcript intron_variant - - - - - - rs7280680 21:45786368 G ENSESTG00000016463 ENSESTT00000041288 Transcript downstream_gene_variant - - - - - - DISTANCE=2203 rs7280680 21:45786368 G 7226 NR_038257.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs915778 21:45790744 T CCDS13710.1 CCDS13710.1 Transcript intron_variant - - - - - - rs915778 21:45790744 T 7226 NM_003307.3 Transcript intron_variant - - - - - - rs915778 21:45790744 T 7226 NR_038257.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1785447 21:45828841 C ENSESTG00000016494 ENSESTT00000041577 Transcript upstream_gene_variant - - - - - - DISTANCE=4856 rs1785447 21:45828841 C CCDS13710.1 CCDS13710.1 Transcript intron_variant - - - - - - rs1785447 21:45828841 C ENSESTG00000016494 ENSESTT00000041567 Transcript upstream_gene_variant - - - - - - DISTANCE=4856 rs1785447 21:45828841 C ENSESTG00000016494 ENSESTT00000041520 Transcript intron_variant - - - - - - rs1785447 21:45828841 C ENSESTG00000016494 ENSESTT00000041561 Transcript upstream_gene_variant - - - - - - DISTANCE=4856 rs1785447 21:45828841 C 7226 NR_038257.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1785447 21:45828841 C ENSESTG00000016494 ENSESTT00000041490 Transcript intron_variant - - - - - - rs1785447 21:45828841 C ENSESTG00000016494 ENSESTT00000041552 Transcript upstream_gene_variant - - - - - - DISTANCE=4856 rs1785447 21:45828841 C 7226 NM_003307.3 Transcript intron_variant - - - - - - rs1785447 21:45828841 C ENSESTG00000016494 ENSESTT00000041503 Transcript intron_variant - - - - - - rs1785447 21:45828841 C ENSESTG00000016494 ENSESTT00000041512 Transcript intron_variant - - - - - - rs233312 21:45904633 G - ENSR00000614707 RegulatoryFeature regulatory_region_variant - - - - - - rs233312 21:45904633 G - - - intergenic_variant - - - - - - rs233229 21:45941286 A CCDS13712.1 CCDS13712.1 Transcript intron_variant - - - - - - rs233229 21:45941286 A ENSESTG00000016687 ENSESTT00000041830 Transcript downstream_gene_variant - - - - - - DISTANCE=2426 rs233229 21:45941286 A 54084 NM_144991.2 Transcript intron_variant - - - - - - rs233229 21:45941286 A 114043 NR_026548.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2426 rs233229 21:45941286 A ENSESTG00000016687 ENSESTT00000041838 Transcript downstream_gene_variant - - - - - - DISTANCE=2647 rs233229 21:45941286 A 114043 NR_026547.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2426 rs365923 21:46031547 C 386681 NM_198695.2 Transcript upstream_gene_variant - - - - - - DISTANCE=449 rs365923 21:46031547 C CCDS13712.1 CCDS13712.1 Transcript intron_variant - - - - - - rs365923 21:46031547 C 54084 NM_144991.2 Transcript intron_variant - - - - - - rs365923 21:46031547 C ENSESTG00000016695 ENSESTT00000041857 Transcript intron_variant - - - - - - rs365923 21:46031547 C CCDS13713.1 CCDS13713.1 Transcript upstream_gene_variant - - - - - - DISTANCE=471 rs1296484 21:46097220 C 353332 NM_181686.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4271 rs1296484 21:46097220 C CCDS42966.1 CCDS42966.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4528 rs1296484 21:46097220 C CCDS13712.1 CCDS13712.1 Transcript intron_variant - - - - - - rs1296484 21:46097220 C 54084 NM_144991.2 Transcript intron_variant - - - - - - rs1296484 21:46097220 C ENSESTG00000016695 ENSESTT00000041857 Transcript intron_variant - - - - - - rs34692724 21:46286532 C ENSESTG00000009372 ENSESTT00000023592 Transcript intron_variant - - - - - - rs34692724 21:46286532 C ENSESTG00000009109 ENSESTT00000022870 Transcript downstream_gene_variant - - - - - - DISTANCE=2886 rs34692724 21:46286532 C ENSESTG00000009372 ENSESTT00000023600 Transcript intron_variant - - - - - - rs34692724 21:46286532 C ENSESTG00000009372 ENSESTT00000023588 Transcript intron_variant - - - - - - rs34692724 21:46286532 C CCDS13715.1 CCDS13715.1 Transcript intron_variant - - - - - - rs34692724 21:46286532 C 754 NM_004339.3 Transcript intron_variant - - - - - - rs235330 21:46314907 A CCDS13716.1 CCDS13716.1 Transcript missense_variant 1062 1062 354 Q/H caA/caT - PolyPhen=possibly_damaging;SIFT=deleterious rs235330 21:46314907 A ENSESTG00000009338 ENSESTT00000023465 Transcript intron_variant - - - - - - rs235330 21:46314907 A ENSESTG00000009338 ENSESTT00000023458 Transcript intron_variant - - - - - - rs235330 21:46314907 A 3689 NM_000211.3 Transcript missense_variant 1295 1062 354 Q/H caA/caT - PolyPhen=possibly_damaging;SIFT=deleterious rs235330 21:46314907 A ENSESTG00000009117 ENSESTT00000022882 Transcript intron_variant - - - - - - rs235330 21:46314907 A 3689 NM_001127491.1 Transcript missense_variant 1250 1062 354 Q/H caA/caT - PolyPhen=possibly_damaging;SIFT=deleterious rs2329942 21:46377365 C CCDS13718.1 CCDS13718.1 Transcript intron_variant - - - - - - rs2329942 21:46377365 C 85395 NM_058190.2 Transcript intron_variant - - - - - - rs2329942 21:46377365 C ENSESTG00000009143 ENSESTT00000022954 Transcript intron_variant - - - - - - rs2329942 21:46377365 C ENSESTG00000009143 ENSESTT00000022946 Transcript intron_variant - - - - - - rs6518209 21:46455617 A - - - intergenic_variant - - - - - - rs4819022 21:46467060 C - - - intergenic_variant - - - - - - rs7279120 21:46491312 T 104 NM_015833.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3181 rs7279120 21:46491312 T 728039 NR_027292.1 Transcript non_coding_exon_variant,nc_transcript_variant 1815 - - - - - rs7279120 21:46491312 T ENSESTG00000009082 ENSESTT00000022815 Transcript upstream_gene_variant - - - - - - DISTANCE=3333 rs7279120 21:46491312 T ENSESTG00000009082 ENSESTT00000022804 Transcript upstream_gene_variant - - - - - - DISTANCE=2456 rs7279120 21:46491312 T 104 NM_015834.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3181 rs7279120 21:46491312 T 104 NM_001160230.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3181 rs7279120 21:46491312 T 104 NR_027674.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3181 rs7279120 21:46491312 T 104 NM_001112.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3181 rs7279120 21:46491312 T ENSESTG00000009082 ENSESTT00000022810 Transcript upstream_gene_variant - - - - - - DISTANCE=3199 rs7279120 21:46491312 T 104 NR_027672.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3181 rs7279120 21:46491312 T 104 NR_027673.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3181 rs914225 21:46829773 G - ENSR00000614878 RegulatoryFeature regulatory_region_variant - - - - - - rs914225 21:46829773 G CCDS42971.1 CCDS42971.1 Transcript intron_variant - - - - - - rs914225 21:46829773 G ENSESTG00000009189 ENSESTT00000023019 Transcript intron_variant - - - - - - rs914225 21:46829773 G 100874236 NR_052004.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs914225 21:46829773 G 80781 NM_130445.2 Transcript intron_variant - - - - - - rs8126682 21:46842099 A 378832 NR_028082.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs8126682 21:46842099 A CCDS42971.1 CCDS42971.1 Transcript intron_variant - - - - - - rs8126682 21:46842099 A ENSESTG00000009189 ENSESTT00000023019 Transcript downstream_gene_variant - - - - - - DISTANCE=2220 rs8126682 21:46842099 A 80781 NM_130445.2 Transcript intron_variant - - - - - - rs8126682 21:46842099 A 378832 NR_027498.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs915807 21:47461396 C - - - intergenic_variant - - - - - - rs62213136 21:47511558 G - - - intergenic_variant - - - - - - rs9983580 21:47820550 C 5116 NM_006031.5 Transcript intron_variant - - - - - - rs9983580 21:47820550 C CCDS33592.1 CCDS33592.1 Transcript intron_variant - - - - - - rs9983580 21:47820550 C ENSESTG00000022747 ENSESTT00000057360 Transcript downstream_gene_variant - - - - - - DISTANCE=875 rs60160543 22:16061250 C - - - intergenic_variant - - - - - - rs5746653 22:17067414 A - ENSR00000672802 RegulatoryFeature regulatory_region_variant - - - - - - rs5746653 22:17067414 A 150160 NM_014406.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4234 rs5746653 22:17067414 A CCDS13738.1 CCDS13738.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4353 rs165673 22:17362751 G - - - intergenic_variant - - - - - - rs5748758 22:17430815 G - - - intergenic_variant - - - - - - rs737965 22:17705033 G ENSESTG00000023461 ENSESTT00000059217 Transcript upstream_gene_variant - - - - - - DISTANCE=4767 rs737965 22:17705033 G ENSESTG00000023461 ENSESTT00000059184 Transcript upstream_gene_variant - - - - - - DISTANCE=2289 rs737964 22:17709760 C - - - intergenic_variant - - - - - - rs2079086 22:17850443 G - ENSR00000615203 RegulatoryFeature regulatory_region_variant - - - - - - rs2079086 22:17850443 G ENSESTG00000001134 ENSESTT00000002706 Transcript intron_variant - - - - - - rs9604733 22:17855552 A ENSESTG00000001134 ENSESTT00000002706 Transcript intron_variant - - - - - - rs1859119 22:17888357 T ENSESTG00000001134 ENSESTT00000002706 Transcript intron_variant - - - - - - rs2158149 22:17909858 A - ENSR00001531072 RegulatoryFeature regulatory_region_variant - - - - - - rs2158149 22:17909858 A ENSESTG00000001134 ENSESTT00000002706 Transcript intron_variant - - - - - - rs2158150 22:17909934 A ENSESTG00000001134 ENSESTT00000002706 Transcript intron_variant - - - - - - rs2522313 22:17909963 A ENSESTG00000001134 ENSESTT00000002706 Transcript intron_variant - - - - - - rs174331 22:18010635 C ENSESTG00000001140 ENSESTT00000002729 Transcript intron_variant - - - - - - rs174331 22:18010635 C ENSESTG00000001140 ENSESTT00000002726 Transcript intron_variant - - - - - - rs174331 22:18010635 C 27443 NM_031413.3 Transcript intron_variant - - - - - - rs174359 22:18044072 G - ENSR00000615216 RegulatoryFeature regulatory_region_variant - - - - - - rs174359 22:18044072 G 83733 NM_031481.1 Transcript intron_variant - - - - - - rs174359 22:18044072 G ENSESTG00000001155 ENSESTT00000002752 Transcript intron_variant - - - - - - rs174359 22:18044072 G ENSESTG00000001155 ENSESTT00000002777 Transcript intron_variant - - - - - - rs174359 22:18044072 G ENSESTG00000001155 ENSESTT00000002756 Transcript intron_variant - - - - - - rs174359 22:18044072 G ENSESTG00000001155 ENSESTT00000002745 Transcript intron_variant - - - - - - rs174359 22:18044072 G ENSESTG00000001155 ENSESTT00000002764 Transcript intron_variant - - - - - - rs174359 22:18044072 G ENSESTG00000001155 ENSESTT00000002742 Transcript intron_variant - - - - - - rs5747254 22:18084001 G CCDS13745.1 CCDS13745.1 Transcript intron_variant - - - - - - rs5747254 22:18084001 G 529 NM_001696.3 Transcript intron_variant - - - - - - rs5747254 22:18084001 G CCDS42977.1 CCDS42977.1 Transcript intron_variant - - - - - - rs5747254 22:18084001 G 529 NM_001039366.1 Transcript intron_variant - - - - - - rs5747254 22:18084001 G ENSESTG00000001346 ENSESTT00000003229 Transcript intron_variant - - - - - - rs5747254 22:18084001 G 529 NM_001039367.1 Transcript intron_variant - - - - - - rs5747254 22:18084001 G CCDS42978.1 CCDS42978.1 Transcript intron_variant - - - - - - rs5747382 22:18346084 G 57553 NM_001136004.1 Transcript 3_prime_UTR_variant 4911 - - - - - rs5747382 22:18346084 G 57553 NM_001122731.1 Transcript intron_variant - - - - - - rs5747382 22:18346084 G 57553 NM_015241.2 Transcript intron_variant - - - - - - rs5747382 22:18346084 G CCDS46659.1 CCDS46659.1 Transcript intron_variant - - - - - - rs5747382 22:18346084 G CCDS46661.1 CCDS46661.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1336 rs5747382 22:18346084 G CCDS46660.1 CCDS46660.1 Transcript intron_variant - - - - - - rs5747382 22:18346084 G ENSESTG00000001312 ENSESTT00000003107 Transcript intron_variant - - - - - - rs361752 22:18622162 T - - - intergenic_variant - - - - - - rs6518523 22:19062460 T 9993 NM_005137.2 Transcript intron_variant - - - - - - rs6518523 22:19062460 T CCDS54496.1 CCDS54496.1 Transcript intron_variant - - - - - - rs6518523 22:19062460 T ENSESTG00000030720 ENSESTT00000077404 Transcript intron_variant - - - - - - rs6518523 22:19062460 T CCDS33598.1 CCDS33598.1 Transcript intron_variant - - - - - - rs6518523 22:19062460 T 9993 NR_033674.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6518523 22:19062460 T ENSESTG00000030720 ENSESTT00000077377 Transcript intron_variant - - - - - - rs6518523 22:19062460 T ENSESTG00000030720 ENSESTT00000077363 Transcript intron_variant - - - - - - rs6518523 22:19062460 T ENSESTG00000030720 ENSESTT00000077392 Transcript intron_variant - - - - - - rs6518523 22:19062460 T 9993 NM_001173534.1 Transcript intron_variant - - - - - - rs6518523 22:19062460 T 9993 NM_001184781.1 Transcript intron_variant - - - - - - rs6518523 22:19062460 T ENSESTG00000030720 ENSESTT00000077317 Transcript intron_variant - - - - - - rs6518523 22:19062460 T ENSESTG00000030720 ENSESTT00000077342 Transcript intron_variant - - - - - - rs6518523 22:19062460 T 9993 NM_001173533.1 Transcript intron_variant - - - - - - rs2525031 22:19069228 A 9993 NM_005137.2 Transcript intron_variant - - - - - - rs2525031 22:19069228 A CCDS54496.1 CCDS54496.1 Transcript intron_variant - - - - - - rs2525031 22:19069228 A ENSESTG00000030720 ENSESTT00000077404 Transcript intron_variant - - - - - - rs2525031 22:19069228 A CCDS33598.1 CCDS33598.1 Transcript intron_variant - - - - - - rs2525031 22:19069228 A 9993 NR_033674.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2525031 22:19069228 A ENSESTG00000030720 ENSESTT00000077377 Transcript intron_variant - - - - - - rs2525031 22:19069228 A ENSESTG00000030720 ENSESTT00000077363 Transcript intron_variant - - - - - - rs2525031 22:19069228 A ENSESTG00000030720 ENSESTT00000077392 Transcript intron_variant - - - - - - rs2525031 22:19069228 A 9993 NM_001173534.1 Transcript intron_variant - - - - - - rs2525031 22:19069228 A 9993 NM_001184781.1 Transcript intron_variant - - - - - - rs2525031 22:19069228 A ENSESTG00000030720 ENSESTT00000077317 Transcript intron_variant - - - - - - rs2525031 22:19069228 A ENSESTG00000030720 ENSESTT00000077342 Transcript intron_variant - - - - - - rs2525031 22:19069228 A 9993 NM_001173533.1 Transcript intron_variant - - - - - - rs2525033 22:19069666 T 9993 NM_005137.2 Transcript intron_variant - - - - - - rs2525033 22:19069666 T CCDS54496.1 CCDS54496.1 Transcript intron_variant - - - - - - rs2525033 22:19069666 T ENSESTG00000030720 ENSESTT00000077404 Transcript intron_variant - - - - - - rs2525033 22:19069666 T CCDS33598.1 CCDS33598.1 Transcript intron_variant - - - - - - rs2525033 22:19069666 T 9993 NR_033674.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2525033 22:19069666 T ENSESTG00000030720 ENSESTT00000077377 Transcript intron_variant - - - - - - rs2525033 22:19069666 T ENSESTG00000030720 ENSESTT00000077363 Transcript intron_variant - - - - - - rs2525033 22:19069666 T ENSESTG00000030720 ENSESTT00000077392 Transcript intron_variant - - - - - - rs2525033 22:19069666 T 9993 NM_001173534.1 Transcript intron_variant - - - - - - rs2525033 22:19069666 T 9993 NM_001184781.1 Transcript intron_variant - - - - - - rs2525033 22:19069666 T ENSESTG00000030720 ENSESTT00000077317 Transcript intron_variant - - - - - - rs2525033 22:19069666 T ENSESTG00000030720 ENSESTT00000077342 Transcript intron_variant - - - - - - rs2525033 22:19069666 T 9993 NM_001173533.1 Transcript intron_variant - - - - - - rs2793077 22:19077902 A 9993 NM_005137.2 Transcript intron_variant - - - - - - rs2793077 22:19077902 A CCDS54496.1 CCDS54496.1 Transcript intron_variant - - - - - - rs2793077 22:19077902 A ENSESTG00000030720 ENSESTT00000077404 Transcript intron_variant - - - - - - rs2793077 22:19077902 A CCDS33598.1 CCDS33598.1 Transcript intron_variant - - - - - - rs2793077 22:19077902 A 9993 NR_033674.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2793077 22:19077902 A ENSESTG00000030720 ENSESTT00000077377 Transcript intron_variant - - - - - - rs2793077 22:19077902 A ENSESTG00000030720 ENSESTT00000077363 Transcript intron_variant - - - - - - rs2793077 22:19077902 A ENSESTG00000030720 ENSESTT00000077392 Transcript intron_variant - - - - - - rs2793077 22:19077902 A 9993 NM_001173534.1 Transcript intron_variant - - - - - - rs2793077 22:19077902 A 9993 NM_001184781.1 Transcript intron_variant - - - - - - rs2793077 22:19077902 A ENSESTG00000030720 ENSESTT00000077317 Transcript intron_variant - - - - - - rs2793077 22:19077902 A ENSESTG00000030720 ENSESTT00000077342 Transcript intron_variant - - - - - - rs2793077 22:19077902 A 9993 NM_001173533.1 Transcript intron_variant - - - - - - rs2793076 22:19078111 A 9993 NM_005137.2 Transcript intron_variant - - - - - - rs2793076 22:19078111 A CCDS54496.1 CCDS54496.1 Transcript intron_variant - - - - - - rs2793076 22:19078111 A ENSESTG00000030720 ENSESTT00000077404 Transcript intron_variant - - - - - - rs2793076 22:19078111 A CCDS33598.1 CCDS33598.1 Transcript intron_variant - - - - - - rs2793076 22:19078111 A 9993 NR_033674.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2793076 22:19078111 A ENSESTG00000030720 ENSESTT00000077377 Transcript intron_variant - - - - - - rs2793076 22:19078111 A ENSESTG00000030720 ENSESTT00000077363 Transcript intron_variant - - - - - - rs2793076 22:19078111 A ENSESTG00000030720 ENSESTT00000077392 Transcript intron_variant - - - - - - rs2793076 22:19078111 A 9993 NM_001173534.1 Transcript intron_variant - - - - - - rs2793076 22:19078111 A 9993 NM_001184781.1 Transcript intron_variant - - - - - - rs2793076 22:19078111 A ENSESTG00000030720 ENSESTT00000077317 Transcript intron_variant - - - - - - rs2793076 22:19078111 A ENSESTG00000030720 ENSESTT00000077342 Transcript intron_variant - - - - - - rs2793076 22:19078111 A 9993 NM_001173533.1 Transcript intron_variant - - - - - - rs2793071 22:19079119 A 9993 NM_005137.2 Transcript intron_variant - - - - - - rs2793071 22:19079119 A CCDS54496.1 CCDS54496.1 Transcript intron_variant - - - - - - rs2793071 22:19079119 A ENSESTG00000030720 ENSESTT00000077404 Transcript intron_variant - - - - - - rs2793071 22:19079119 A CCDS33598.1 CCDS33598.1 Transcript intron_variant - - - - - - rs2793071 22:19079119 A 9993 NR_033674.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2793071 22:19079119 A ENSESTG00000030720 ENSESTT00000077377 Transcript intron_variant - - - - - - rs2793071 22:19079119 A ENSESTG00000030720 ENSESTT00000077363 Transcript intron_variant - - - - - - rs2793071 22:19079119 A ENSESTG00000030720 ENSESTT00000077392 Transcript intron_variant - - - - - - rs2793071 22:19079119 A 9993 NM_001173534.1 Transcript intron_variant - - - - - - rs2793071 22:19079119 A 9993 NM_001184781.1 Transcript intron_variant - - - - - - rs2793071 22:19079119 A ENSESTG00000030720 ENSESTT00000077317 Transcript intron_variant - - - - - - rs2793071 22:19079119 A ENSESTG00000030720 ENSESTT00000077342 Transcript intron_variant - - - - - - rs2793071 22:19079119 A 9993 NM_001173533.1 Transcript intron_variant - - - - - - rs807676 22:19152824 A - - - intergenic_variant - - - - - - rs1548360 22:19370339 A 7290 NM_003325.3 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000076957 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000076943 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000077061 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000076920 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000077057 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000077029 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000077045 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000077034 Transcript intron_variant - - - - - - rs1548360 22:19370339 A CCDS13759.1 CCDS13759.1 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000077043 Transcript intron_variant - - - - - - rs1548360 22:19370339 A ENSESTG00000030475 ENSESTT00000076950 Transcript intron_variant - - - - - - rs4819801 22:19378255 G - ENSR00000672871 RegulatoryFeature regulatory_region_variant - - - - - - rs4819801 22:19378255 G 7290 NM_003325.3 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000076957 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000076943 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000077061 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000076920 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000077057 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000077029 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000077045 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000077034 Transcript intron_variant - - - - - - rs4819801 22:19378255 G CCDS13759.1 CCDS13759.1 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000077043 Transcript intron_variant - - - - - - rs4819801 22:19378255 G ENSESTG00000030475 ENSESTT00000076950 Transcript intron_variant - - - - - - rs4819513 22:19523946 T - - - intergenic_variant - - - - - - rs5746796 22:19586351 C - ENSR00000615425 RegulatoryFeature regulatory_region_variant - - - - - - rs5746796 22:19586351 C - - - intergenic_variant - - - - - - rs11089306 22:19743115 C - ENSR00001041719 RegulatoryFeature regulatory_region_variant - - - - - - rs11089306 22:19743115 C 6899 NM_005992.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1111 rs11089306 22:19743115 C CCDS13767.1 CCDS13767.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4052 rs11089306 22:19743115 C CCDS13765.1 CCDS13765.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4052 rs11089306 22:19743115 C CCDS13766.1 CCDS13766.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4052 rs11089306 22:19743115 C 6899 NM_080646.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1111 rs11089306 22:19743115 C 6899 NM_080647.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1111 rs756659 22:19785127 C - ENSR00000291329 RegulatoryFeature regulatory_region_variant - - - - - - rs756659 22:19785127 C ENSESTG00000012743 ENSESTT00000032010 Transcript intron_variant - - - - - - rs756659 22:19785127 C 54584 NM_053004.2 Transcript intron_variant - - - - - - rs756659 22:19785127 C CCDS13768.1 CCDS13768.1 Transcript intron_variant - - - - - - rs756659 22:19785127 C ENSESTG00000013556 ENSESTT00000033917 Transcript intron_variant - - - - - - rs9605022 22:19848447 T - - - intergenic_variant - - - - - - rs4819524 22:19852056 T - ENSR00001531222 RegulatoryFeature regulatory_region_variant - - - - - - rs4819524 22:19852056 T - - - intergenic_variant - - - - - - rs174888 22:20071361 A - ENSR00000291508 RegulatoryFeature regulatory_region_variant - - - - - - rs174888 22:20071361 A ENSESTG00000012964 ENSESTT00000032548 Transcript upstream_gene_variant - - - - - - DISTANCE=3225 rs174888 22:20071361 A 100500860 NR_037412.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1908 rs174888 22:20071361 A 54487 NM_022720.6 Transcript intron_variant - - - - - - rs174888 22:20071361 A 100302197 NR_031706.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2220 rs174888 22:20071361 A CCDS54501.1 CCDS54501.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2126 rs174888 22:20071361 A ENSESTG00000012964 ENSESTT00000032540 Transcript intron_variant - - - - - - rs174888 22:20071361 A CCDS13773.1 CCDS13773.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2126 rs174888 22:20071361 A 54487 NM_001190326.1 Transcript intron_variant - - - - - - rs174888 22:20071361 A ENSESTG00000012964 ENSESTT00000032545 Transcript upstream_gene_variant - - - - - - DISTANCE=2820 rs641263 22:20186654 G ENSESTG00000013105 ENSESTT00000032845 Transcript intron_variant - - - - - - rs641263 22:20186654 G 284865 NR_038460.1 Transcript non_coding_exon_variant,nc_transcript_variant 1826 - - - - - rs587317 22:20202667 C - - - intergenic_variant - - - - - - rs587719 22:20202714 G - - - intergenic_variant - - - - - - rs1642171 22:20206052 C - ENSR00000291610 RegulatoryFeature regulatory_region_variant - - - - - - rs1642171 22:20206052 C - - - intergenic_variant - - - - - - rs854963 22:20213720 T - ENSR00000291616 RegulatoryFeature regulatory_region_variant - - - - - - rs854963 22:20213720 T - - - intergenic_variant - - - - - - rs696882 22:20220337 C - - - intergenic_variant - - - - - - rs854929 22:20255020 C - ENSR00000169453 RegulatoryFeature regulatory_region_variant - - - - - - rs854929 22:20255020 C ENSESTG00000013342 ENSESTT00000033469 Transcript intron_variant - - - - - - rs854929 22:20255020 C ENSESTG00000013342 ENSESTT00000033474 Transcript intron_variant - - - - - - rs854929 22:20255020 C ENSESTG00000013342 ENSESTT00000033471 Transcript intron_variant - - - - - - rs854929 22:20255020 C CCDS13777.1 CCDS13777.1 Transcript intron_variant - - - - - - rs854929 22:20255020 C 65078 NM_023004.5 Transcript intron_variant - - - - - - rs854929 22:20255020 C ENSESTG00000013342 ENSESTT00000033476 Transcript intron_variant - - - - - - rs673440 22:20985783 G - - - intergenic_variant - - - - - - rs633773 22:20991578 G - - - intergenic_variant - - - - - - rs165831 22:21137813 G CCDS13783.1 CCDS13783.1 Transcript intron_variant - - - - - - rs165831 22:21137813 G ENSESTG00000005150 ENSESTT00000013158 Transcript intron_variant - - - - - - rs165831 22:21137813 G ENSESTG00000004864 ENSESTT00000012337 Transcript intron_variant - - - - - - rs165831 22:21137813 G 3053 NM_000185.3 Transcript intron_variant - - - - - - rs165831 22:21137813 G ENSESTG00000005150 ENSESTT00000013148 Transcript intron_variant - - - - - - rs165831 22:21137813 G 5297 NM_058004.3 Transcript intron_variant - - - - - - rs165831 22:21137813 G ENSESTG00000004864 ENSESTT00000012341 Transcript intron_variant - - - - - - rs165831 22:21137813 G CCDS33603.2 CCDS33603.2 Transcript intron_variant - - - - - - rs165831 22:21137813 G ENSESTG00000005150 ENSESTT00000013165 Transcript upstream_gene_variant - - - - - - DISTANCE=3937 rs165831 22:21137813 G ENSESTG00000005185 ENSESTT00000013175 Transcript intron_variant - - - - - - rs165831 22:21137813 G ENSESTG00000005150 ENSESTT00000013135 Transcript intron_variant - - - - - - rs165831 22:21137813 G ENSESTG00000004855 ENSESTT00000012331 Transcript downstream_gene_variant - - - - - - DISTANCE=3721 rs178257 22:21323070 C 150209 NR_027464.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs178257 22:21323070 C ENSESTG00000004902 ENSESTT00000012518 Transcript intron_variant - - - - - - rs178257 22:21323070 C ENSESTG00000004890 ENSESTT00000012431 Transcript downstream_gene_variant - - - - - - DISTANCE=1983 rs178257 22:21323070 C ENSESTG00000004882 ENSESTT00000012415 Transcript downstream_gene_variant - - - - - - DISTANCE=4103 rs178257 22:21323070 C CCDS13786.1 CCDS13786.1 Transcript intron_variant - - - - - - rs178257 22:21323070 C ENSESTG00000004902 ENSESTT00000012528 Transcript intron_variant - - - - - - rs178257 22:21323070 C CCDS33605.1 CCDS33605.1 Transcript intron_variant - - - - - - rs178257 22:21323070 C 150209 NM_001146288.1 Transcript intron_variant - - - - - - rs178257 22:21323070 C CCDS54503.1 CCDS54503.1 Transcript intron_variant - - - - - - rs178257 22:21323070 C ENSESTG00000004902 ENSESTT00000012537 Transcript intron_variant - - - - - - rs178257 22:21323070 C ENSESTG00000004902 ENSESTT00000012534 Transcript intron_variant - - - - - - rs178257 22:21323070 C ENSESTG00000004902 ENSESTT00000012535 Transcript intron_variant - - - - - - rs178257 22:21323070 C 150209 NM_001018060.2 Transcript intron_variant - - - - - - rs178257 22:21323070 C 150209 NM_144704.2 Transcript intron_variant - - - - - - rs178257 22:21323070 C ENSESTG00000004902 ENSESTT00000012532 Transcript intron_variant - - - - - - rs178269 22:21331043 T - ENSR00000291988 RegulatoryFeature regulatory_region_variant - - - - - - rs178269 22:21331043 T ENSESTG00000004902 ENSESTT00000012518 Transcript synonymous_variant 1278 549 183 R cgA/cgT - rs178269 22:21331043 T CCDS13786.1 CCDS13786.1 Transcript synonymous_variant 1134 1134 378 R cgA/cgT - rs178269 22:21331043 T 150209 NM_001146288.1 Transcript synonymous_variant 1437 1152 384 R cgA/cgT - rs178269 22:21331043 T CCDS54503.1 CCDS54503.1 Transcript synonymous_variant 1152 1152 384 R cgA/cgT - rs178269 22:21331043 T ENSESTG00000004902 ENSESTT00000012542 Transcript synonymous_variant 612 570 190 R cgA/cgT - rs178269 22:21331043 T ENSESTG00000004902 ENSESTT00000012534 Transcript synonymous_variant 1324 549 183 R cgA/cgT - rs178269 22:21331043 T 150209 NM_144704.2 Transcript synonymous_variant 1352 1134 378 R cgA/cgT - rs178269 22:21331043 T 150209 NR_027464.1 Transcript non_coding_exon_variant,nc_transcript_variant 1309 - - - - - rs178269 22:21331043 T ENSESTG00000004902 ENSESTT00000012528 Transcript synonymous_variant 1278 549 183 R cgA/cgT - rs178269 22:21331043 T ENSESTG00000004902 ENSESTT00000012541 Transcript synonymous_variant 612 570 190 R cgA/cgT - rs178269 22:21331043 T CCDS33605.1 CCDS33605.1 Transcript synonymous_variant 1134 1134 378 R cgA/cgT - rs178269 22:21331043 T ENSESTG00000004902 ENSESTT00000012537 Transcript synonymous_variant 1292 549 183 R cgA/cgT - rs178269 22:21331043 T ENSESTG00000004902 ENSESTT00000012535 Transcript synonymous_variant 1292 549 183 R cgA/cgT - rs178269 22:21331043 T 150209 NM_001018060.2 Transcript synonymous_variant 1352 1134 378 R cgA/cgT - rs178269 22:21331043 T ENSESTG00000004902 ENSESTT00000012545 Transcript upstream_gene_variant - - - - - - DISTANCE=861 rs178269 22:21331043 T ENSESTG00000004902 ENSESTT00000012532 Transcript synonymous_variant 1324 549 183 R cgA/cgT - rs178281 22:21337415 G - ENSR00001531302 RegulatoryFeature regulatory_region_variant - - - - - - rs178281 22:21337415 G ENSESTG00000004902 ENSESTT00000012518 Transcript downstream_gene_variant - - - - - - DISTANCE=1766 rs178281 22:21337415 G ENSESTG00000004946 ENSESTT00000012648 Transcript intron_variant - - - - - - rs178281 22:21337415 G CCDS13786.1 CCDS13786.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2095 rs178281 22:21337415 G 150209 NM_001146288.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1766 rs178281 22:21337415 G CCDS54503.1 CCDS54503.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2095 rs178281 22:21337415 G 150209 NM_144704.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1766 rs178281 22:21337415 G CCDS33606.1 CCDS33606.1 Transcript intron_variant - - - - - - rs178281 22:21337415 G 150209 NR_027464.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1766 rs178281 22:21337415 G ENSESTG00000004902 ENSESTT00000012541 Transcript downstream_gene_variant - - - - - - DISTANCE=1766 rs178281 22:21337415 G ENSESTG00000004946 ENSESTT00000012639 Transcript intron_variant - - - - - - rs178281 22:21337415 G CCDS33605.1 CCDS33605.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2095 rs178281 22:21337415 G ENSESTG00000004946 ENSESTT00000012644 Transcript intron_variant - - - - - - rs178281 22:21337415 G ENSESTG00000004946 ENSESTT00000012653 Transcript upstream_gene_variant - - - - - - DISTANCE=2953 rs178281 22:21337415 G ENSESTG00000004902 ENSESTT00000012535 Transcript downstream_gene_variant - - - - - - DISTANCE=1766 rs178281 22:21337415 G 8216 NM_006767.3 Transcript intron_variant - - - - - - rs178281 22:21337415 G 150209 NM_001018060.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1766 rs178281 22:21337415 G ENSESTG00000004902 ENSESTT00000012545 Transcript downstream_gene_variant - - - - - - DISTANCE=2770 rs178281 22:21337415 G ENSESTG00000004946 ENSESTT00000012651 Transcript upstream_gene_variant - - - - - - DISTANCE=2953 rs178281 22:21337415 G ENSESTG00000004902 ENSESTT00000012532 Transcript downstream_gene_variant - - - - - - DISTANCE=1766 rs364962 22:21976407 G CCDS58796.1 CCDS58796.1 Transcript downstream_gene_variant - - - - - - DISTANCE=449 rs364962 22:21976407 G CCDS58795.1 CCDS58795.1 Transcript downstream_gene_variant - - - - - - DISTANCE=449 rs364962 22:21976407 G ENSESTG00000030615 ENSESTT00000077160 Transcript downstream_gene_variant - - - - - - DISTANCE=246 rs364962 22:21976407 G ENSESTG00000030615 ENSESTT00000077187 Transcript downstream_gene_variant - - - - - - DISTANCE=246 rs364962 22:21976407 G ENSESTG00000030615 ENSESTT00000077199 Transcript downstream_gene_variant - - - - - - DISTANCE=526 rs364962 22:21976407 G ENSESTG00000030615 ENSESTT00000077210 Transcript downstream_gene_variant - - - - - - DISTANCE=246 rs364962 22:21976407 G 7332 NR_046082.1 Transcript non_coding_exon_variant,nc_transcript_variant 1535 - - - - - rs364962 22:21976407 G 7332 NM_003347.3 Transcript 3_prime_UTR_variant 1112 - - - - - rs364962 22:21976407 G 7332 NM_001256356.1 Transcript 3_prime_UTR_variant 1016 - - - - - rs364962 22:21976407 G 7332 NR_028436.2 Transcript non_coding_exon_variant,nc_transcript_variant 1221 - - - - - rs364962 22:21976407 G ENSESTG00000031202 ENSESTT00000078597 Transcript downstream_gene_variant - - - - - - DISTANCE=4451 rs364962 22:21976407 G CCDS13790.1 CCDS13790.1 Transcript downstream_gene_variant - - - - - - DISTANCE=449 rs364962 22:21976407 G 7332 NM_001256355.1 Transcript 3_prime_UTR_variant 1091 - - - - - rs238774 22:22348689 G - ENSR00000292414 RegulatoryFeature regulatory_region_variant - - - - - - rs238774 22:22348689 G - - - intergenic_variant - - - - - - rs441724 22:22361242 C - - - intergenic_variant - - - - - - rs424530 22:22380066 G - ENSR00001041487 RegulatoryFeature regulatory_region_variant - - - - - - rs424530 22:22380066 G ENSESTG00000030989 ENSESTT00000078002 Transcript downstream_gene_variant - - - - - - DISTANCE=253 rs424530 22:22380066 G 28763 NC_000022.10:IGLVI-70:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=408 rs5756915 22:22472954 A - ENSR00000169547 RegulatoryFeature regulatory_region_variant - - - - - - rs5756915 22:22472954 A - - - intergenic_variant - - - - - - rs987709 22:22512215 G - ENSR00000292472 RegulatoryFeature regulatory_region_variant - - - - - - rs987709 22:22512215 G 28785 NC_000022.10:IGLV4-60:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4376 rs2040344 22:22561132 G - ENSR00000292485 RegulatoryFeature regulatory_region_variant - - - - - - rs2040344 22:22561132 G 28770 NC_000022.10:IGLV11-55:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4577 rs1029265 22:22567844 G - ENSR00000615670 RegulatoryFeature regulatory_region_variant - - - - - - rs1029265 22:22567844 G 28772 NC_000022.10:IGLV10-54:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1353 rs6001607 22:22611290 C - - - intergenic_variant - - - - - - rs738896 22:22684088 G 28821 NC_000022.10:IGLV1-50:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1914 rs1894246 22:22698027 G - ENSR00000084570 RegulatoryFeature regulatory_region_variant - - - - - - rs1894246 22:22698027 G 28773 NC_000022.10:IGLV9-49:u_t_1 Transcript synonymous_variant 315 315 105 E gaA/gaG - rs178431 22:22793621 C - - - intergenic_variant - - - - - - rs416630 22:22901579 G - ENSR00000292545 RegulatoryFeature regulatory_region_variant - - - - - - rs416630 22:22901579 G 23532 NM_206953.1 Transcript splice_region_variant,intron_variant - - - - - - rs416630 22:22901579 G 648691 NR_027426.1 Transcript upstream_gene_variant - - - - - - DISTANCE=177 rs416630 22:22901579 G 23532 NM_006115.3 Transcript splice_region_variant,intron_variant - - - - - - rs416630 22:22901579 G 23532 NM_206955.1 Transcript upstream_gene_variant - - - - - - DISTANCE=29 rs416630 22:22901579 G ENSESTG00000030834 ENSESTT00000077777 Transcript upstream_gene_variant - - - - - - DISTANCE=161 rs416630 22:22901579 G CCDS13801.1 CCDS13801.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2327 rs416630 22:22901579 G ENSESTG00000030834 ENSESTT00000077769 Transcript splice_region_variant,intron_variant - - - - - - rs416630 22:22901579 G 23532 NM_206954.1 Transcript splice_region_variant,intron_variant - - - - - - rs416630 22:22901579 G 23532 NM_206956.1 Transcript upstream_gene_variant - - - - - - DISTANCE=29 rs416630 22:22901579 G ENSESTG00000030834 ENSESTT00000077752 Transcript splice_region_variant,intron_variant - - - - - - rs457586 22:22998475 G - ENSR00000292580 RegulatoryFeature regulatory_region_variant - - - - - - rs457586 22:22998475 G 28790 NC_000022.10:IGLV3-29:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4944 rs110431 22:23079472 T 28814 NC_000022.10:IGLV2-18:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1895 rs110431 22:23079472 T ENSESTG00000030414 ENSESTT00000076600 Transcript intron_variant - - - - - - rs110431 22:23079472 T ENSESTG00000030414 ENSESTT00000076568 Transcript intron_variant - - - - - - rs110431 22:23079472 T 28798 NC_000022.10:IGLV3-17:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=1927 rs110431 22:23079472 T ENSESTG00000030414 ENSESTT00000076552 Transcript intron_variant - - - - - - rs5996396 22:23164936 G 723778 NR_030755.1 Transcript upstream_gene_variant - - - - - - DISTANCE=334 rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076690 Transcript intron_variant - - - - - - rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076600 Transcript intron_variant - - - - - - rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076754 Transcript intron_variant - - - - - - rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076730 Transcript intron_variant - - - - - - rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076568 Transcript intron_variant - - - - - - rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076552 Transcript intron_variant - - - - - - rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076774 Transcript intron_variant - - - - - - rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076673 Transcript intron_variant - - - - - - rs5996396 22:23164936 G 28804 NC_000022.10:IGLV3-9:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2687 rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076735 Transcript intron_variant - - - - - - rs5996396 22:23164936 G ENSESTG00000030414 ENSESTT00000076814 Transcript upstream_gene_variant - - - - - - DISTANCE=818 rs5996396 22:23164936 G 28817 NC_000022.10:IGLV2-8:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=379 rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076690 Transcript intron_variant - - - - - - rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076600 Transcript intron_variant - - - - - - rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076754 Transcript intron_variant - - - - - - rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076730 Transcript intron_variant - - - - - - rs367954 22:23202138 G ENSESTG00000030831 ENSESTT00000077637 Transcript downstream_gene_variant - - - - - - DISTANCE=2529 rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076568 Transcript intron_variant - - - - - - rs367954 22:23202138 G 28807 NC_000022.10:IGLV3-4:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1661 rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076552 Transcript intron_variant - - - - - - rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076774 Transcript intron_variant - - - - - - rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076673 Transcript intron_variant - - - - - - rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076735 Transcript intron_variant - - - - - - rs367954 22:23202138 G ENSESTG00000030414 ENSESTT00000076814 Transcript intron_variant - - - - - - rs367954 22:23202138 G 28818 NC_000022.10:IGLV2-5:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=2903 rs368464 22:23226852 T - ENSR00000292705 RegulatoryFeature regulatory_region_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076754 Transcript intron_variant - - - - - - rs368464 22:23226852 T 28809 NC_000022.10:IGLV3-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=3280 rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076568 Transcript intron_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076552 Transcript intron_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076673 Transcript intron_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076897 Transcript upstream_gene_variant - - - - - - DISTANCE=3168 rs368464 22:23226852 T 100423062 NM_001256296.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3108 rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076690 Transcript intron_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076600 Transcript intron_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076730 Transcript intron_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076904 Transcript upstream_gene_variant - - - - - - DISTANCE=3168 rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076774 Transcript intron_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076838 Transcript intron_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076878 Transcript intron_variant - - - - - - rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076735 Transcript intron_variant - - - - - - rs368464 22:23226852 T 100423062 NM_001178126.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3108 rs368464 22:23226852 T ENSESTG00000030414 ENSESTT00000076814 Transcript intron_variant - - - - - - rs368464 22:23226852 T CCDS54506.1 CCDS54506.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3382 rs361936 22:23253270 C - ENSR00000292726 RegulatoryFeature regulatory_region_variant - - - - - - rs361936 22:23253270 C 28830 NC_000022.10:IGLJ4:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=493 rs361936 22:23253270 C ENSESTG00000030826 ENSESTT00000077630 Transcript upstream_gene_variant - - - - - - DISTANCE=4303 rs361936 22:23253270 C ENSESTG00000030414 ENSESTT00000076600 Transcript intron_variant - - - - - - rs361936 22:23253270 C ENSESTG00000030414 ENSESTT00000076730 Transcript intron_variant - - - - - - rs361936 22:23253270 C ENSESTG00000030826 ENSESTT00000077623 Transcript upstream_gene_variant - - - - - - DISTANCE=4302 rs361936 22:23253270 C ENSESTG00000030826 ENSESTT00000077617 Transcript upstream_gene_variant - - - - - - DISTANCE=4302 rs361936 22:23253270 C ENSESTG00000030414 ENSESTT00000076568 Transcript downstream_gene_variant - - - - - - DISTANCE=4297 rs361936 22:23253270 C ENSESTG00000030414 ENSESTT00000076948 Transcript downstream_gene_variant - - - - - - DISTANCE=4306 rs361936 22:23253270 C ENSESTG00000030414 ENSESTT00000076552 Transcript downstream_gene_variant - - - - - - DISTANCE=4297 rs361936 22:23253270 C 3541 NC_000022.10:IGLC5:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4524 rs361936 22:23253270 C 3539 NC_000022.10:IGLC3:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=4439 rs361936 22:23253270 C ENSESTG00000030414 ENSESTT00000076838 Transcript downstream_gene_variant - - - - - - DISTANCE=4606 rs361936 22:23253270 C 3540 NC_000022.10:IGLC4:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=20 rs361936 22:23253270 C 28829 NC_000022.10:IGLJ5:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=3173 rs2330360 22:23512338 A - - - intergenic_variant - - - - - - rs738908 22:23570416 A ENSESTG00000030632 ENSESTT00000077393 Transcript intron_variant - - - - - - rs738908 22:23570416 A ENSESTG00000030632 ENSESTT00000077371 Transcript intron_variant - - - - - - rs738908 22:23570416 A CCDS13806.1 CCDS13806.1 Transcript intron_variant - - - - - - rs738908 22:23570416 A CCDS13807.1 CCDS13807.1 Transcript intron_variant - - - - - - rs738908 22:23570416 A 613 NM_004327.3 Transcript intron_variant - - - - - - rs738908 22:23570416 A 613 NM_021574.2 Transcript intron_variant - - - - - - rs738908 22:23570416 A ENSESTG00000030632 ENSESTT00000077362 Transcript intron_variant - - - - - - rs738908 22:23570416 A ENSESTG00000030632 ENSESTT00000077398 Transcript intron_variant - - - - - - rs2097218 22:23570871 T ENSESTG00000030632 ENSESTT00000077393 Transcript intron_variant - - - - - - rs2097218 22:23570871 T ENSESTG00000030632 ENSESTT00000077371 Transcript intron_variant - - - - - - rs2097218 22:23570871 T CCDS13806.1 CCDS13806.1 Transcript intron_variant - - - - - - rs2097218 22:23570871 T CCDS13807.1 CCDS13807.1 Transcript intron_variant - - - - - - rs2097218 22:23570871 T 613 NM_004327.3 Transcript intron_variant - - - - - - rs2097218 22:23570871 T 613 NM_021574.2 Transcript intron_variant - - - - - - rs2097218 22:23570871 T ENSESTG00000030632 ENSESTT00000077362 Transcript intron_variant - - - - - - rs2097218 22:23570871 T ENSESTG00000030632 ENSESTT00000077398 Transcript intron_variant - - - - - - rs28375 22:23585311 C - ENSR00000169594 RegulatoryFeature regulatory_region_variant - - - - - - rs28375 22:23585311 C ENSESTG00000030632 ENSESTT00000077393 Transcript intron_variant - - - - - - rs28375 22:23585311 C ENSESTG00000030632 ENSESTT00000077371 Transcript intron_variant - - - - - - rs28375 22:23585311 C CCDS13806.1 CCDS13806.1 Transcript intron_variant - - - - - - rs28375 22:23585311 C CCDS13807.1 CCDS13807.1 Transcript intron_variant - - - - - - rs28375 22:23585311 C 613 NM_004327.3 Transcript intron_variant - - - - - - rs28375 22:23585311 C 613 NM_021574.2 Transcript intron_variant - - - - - - rs28375 22:23585311 C ENSESTG00000030632 ENSESTT00000077362 Transcript intron_variant - - - - - - rs28375 22:23585311 C ENSESTG00000030632 ENSESTT00000077398 Transcript intron_variant - - - - - - rs131675 22:23627441 C - ENSR00000292926 RegulatoryFeature regulatory_region_variant - - - - - - rs131675 22:23627441 C ENSESTG00000030632 ENSESTT00000077393 Transcript intron_variant - - - - - - rs131675 22:23627441 C ENSESTG00000030632 ENSESTT00000077371 Transcript intron_variant - - - - - - rs131675 22:23627441 C CCDS13806.1 CCDS13806.1 Transcript intron_variant - - - - - - rs131675 22:23627441 C ENSESTG00000030632 ENSESTT00000077439 Transcript intron_variant - - - - - - rs131675 22:23627441 C ENSESTG00000030632 ENSESTT00000077469 Transcript intron_variant - - - - - - rs131675 22:23627441 C ENSESTG00000030632 ENSESTT00000077460 Transcript intron_variant - - - - - - rs131675 22:23627441 C ENSESTG00000030632 ENSESTT00000077481 Transcript intron_variant - - - - - - rs131675 22:23627441 C CCDS13807.1 CCDS13807.1 Transcript intron_variant - - - - - - rs131675 22:23627441 C 613 NM_004327.3 Transcript intron_variant - - - - - - rs131675 22:23627441 C ENSESTG00000030632 ENSESTT00000077449 Transcript intron_variant - - - - - - rs131675 22:23627441 C 613 NM_021574.2 Transcript intron_variant - - - - - - rs131675 22:23627441 C ENSESTG00000030632 ENSESTT00000077362 Transcript intron_variant - - - - - - rs131675 22:23627441 C ENSESTG00000030632 ENSESTT00000077398 Transcript intron_variant - - - - - - rs2032113 22:23804307 G ENSESTG00000011146 ENSESTT00000027977 Transcript downstream_gene_variant - - - - - - DISTANCE=867 rs2032113 22:23804307 G ENSESTG00000011146 ENSESTT00000027976 Transcript downstream_gene_variant - - - - - - DISTANCE=867 rs933132 22:24051972 C ENSESTG00000011604 ENSESTT00000029101 Transcript downstream_gene_variant - - - - - - DISTANCE=4456 rs933132 22:24051972 C 91316 NR_024448.2 Transcript splice_donor_variant,nc_transcript_variant - - - - - - rs933132 22:24051972 C ENSESTG00000011604 ENSESTT00000029105 Transcript downstream_gene_variant - - - - - - DISTANCE=4513 rs204710 22:24717850 G ENSESTG00000018095 ENSESTT00000045701 Transcript upstream_gene_variant - - - - - - DISTANCE=146 rs204710 22:24717850 G CCDS33619.1 CCDS33619.1 Transcript missense_variant 902 902 301 D/G gAt/gGt - PolyPhen=benign;SIFT=tolerated rs204710 22:24717850 G CCDS58797.1 CCDS58797.1 Transcript missense_variant 902 902 301 D/G gAt/gGt - PolyPhen=benign;SIFT=tolerated rs204710 22:24717850 G 23384 NM_001145468.2 Transcript missense_variant 1101 902 301 D/G gAt/gGt - PolyPhen=benign;SIFT=tolerated rs204710 22:24717850 G 23384 NM_001254732.1 Transcript missense_variant 1101 902 301 D/G gAt/gGt - PolyPhen=benign;SIFT=tolerated rs204710 22:24717850 G ENSESTG00000018066 ENSESTT00000045481 Transcript downstream_gene_variant - - - - - - DISTANCE=495 rs204710 22:24717850 G 23384 NM_015330.3 Transcript missense_variant 1205 902 301 D/G gAt/gGt - PolyPhen=benign;SIFT=tolerated rs204710 22:24717850 G ENSESTG00000018066 ENSESTT00000045513 Transcript downstream_gene_variant - - - - - - DISTANCE=194 rs4820592 22:24886650 T ENSESTG00000018260 ENSESTT00000046070 Transcript upstream_gene_variant - - - - - - DISTANCE=4622 rs4820592 22:24886650 T ENSESTG00000018260 ENSESTT00000046147 Transcript upstream_gene_variant - - - - - - DISTANCE=4654 rs4820592 22:24886650 T 646023 NR_028484.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4820592 22:24886650 T 51733 NM_016327.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4601 rs4820592 22:24886650 T ENSESTG00000018260 ENSESTT00000046166 Transcript upstream_gene_variant - - - - - - DISTANCE=4654 rs4820592 22:24886650 T 646023 NR_028483.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4820592 22:24886650 T ENSESTG00000018883 ENSESTT00000047562 Transcript intron_variant - - - - - - rs4820592 22:24886650 T ENSESTG00000018883 ENSESTT00000047575 Transcript intron_variant - - - - - - rs4820592 22:24886650 T ENSESTG00000018232 ENSESTT00000045951 Transcript intron_variant - - - - - - rs4820592 22:24886650 T CCDS13827.1 CCDS13827.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4722 rs4820592 22:24886650 T ENSESTG00000018260 ENSESTT00000046193 Transcript upstream_gene_variant - - - - - - DISTANCE=4654 rs738328 22:25408169 C - - - intergenic_variant - - - - - - rs133169 22:25723202 G ENSESTG00000007423 ENSESTT00000018682 Transcript intron_variant - - - - - - rs133169 22:25723202 G ENSESTG00000007423 ENSESTT00000018670 Transcript intron_variant - - - - - - rs133169 22:25723202 G ENSESTG00000007229 ENSESTT00000018221 Transcript upstream_gene_variant - - - - - - DISTANCE=53 rs133169 22:25723202 G ENSESTG00000007434 ENSESTT00000018701 Transcript intron_variant - - - - - - rs473652 22:25873143 G ENSESTG00000007239 ENSESTT00000018280 Transcript intron_variant - - - - - - rs473652 22:25873143 G ENSESTG00000007423 ENSESTT00000018670 Transcript upstream_gene_variant - - - - - - DISTANCE=1603 rs473652 22:25873143 G ENSESTG00000007266 ENSESTT00000018332 Transcript intron_variant - - - - - - rs630302 22:25875717 A ENSESTG00000007239 ENSESTT00000018280 Transcript intron_variant - - - - - - rs630302 22:25875717 A ENSESTG00000007423 ENSESTT00000018670 Transcript upstream_gene_variant - - - - - - DISTANCE=4177 rs630302 22:25875717 A ENSESTG00000007266 ENSESTT00000018332 Transcript 3_prime_UTR_variant 1175 - - - - - rs4822650 22:26163085 C CCDS54507.1 CCDS54507.1 Transcript intron_variant - - - - - - rs4822650 22:26163085 C ENSESTG00000007314 ENSESTT00000018435 Transcript downstream_gene_variant - - - - - - DISTANCE=3866 rs4822650 22:26163085 C 84700 NM_032608.5 Transcript intron_variant - - - - - - rs5752208 22:26185203 T ENSESTG00000007323 ENSESTT00000018450 Transcript intron_variant - - - - - - rs5752208 22:26185203 T CCDS54507.1 CCDS54507.1 Transcript intron_variant - - - - - - rs5752208 22:26185203 T 84700 NM_032608.5 Transcript intron_variant - - - - - - rs132494 22:26403241 G CCDS54507.1 CCDS54507.1 Transcript intron_variant - - - - - - rs132494 22:26403241 G ENSESTG00000007340 ENSESTT00000018506 Transcript intron_variant - - - - - - rs132494 22:26403241 G 84700 NM_032608.5 Transcript intron_variant - - - - - - rs4822690 22:26588117 C CCDS54508.1 CCDS54508.1 Transcript intron_variant - - - - - - rs4822690 22:26588117 C 23544 NM_001184774.1 Transcript intron_variant - - - - - - rs4822690 22:26588117 C 23544 NM_001184776.1 Transcript intron_variant - - - - - - rs4822690 22:26588117 C CCDS54510.1 CCDS54510.1 Transcript intron_variant - - - - - - rs4822690 22:26588117 C CCDS54511.1 CCDS54511.1 Transcript intron_variant - - - - - - rs4822690 22:26588117 C 23544 NM_021115.4 Transcript intron_variant - - - - - - rs4822690 22:26588117 C ENSESTG00000007370 ENSESTT00000018545 Transcript intron_variant - - - - - - rs4822690 22:26588117 C CCDS54509.1 CCDS54509.1 Transcript intron_variant - - - - - - rs4822690 22:26588117 C 23544 NM_001184775.1 Transcript intron_variant - - - - - - rs4822690 22:26588117 C CCDS13833.1 CCDS13833.1 Transcript intron_variant - - - - - - rs4822690 22:26588117 C 23544 NM_001184777.1 Transcript intron_variant - - - - - - rs4822690 22:26588117 C 23544 NM_001184773.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C CCDS54508.1 CCDS54508.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C 23544 NM_001184774.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C 23544 NM_001184776.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C CCDS54510.1 CCDS54510.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C CCDS54511.1 CCDS54511.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C 23544 NM_021115.4 Transcript intron_variant - - - - - - rs5761422 22:26624528 C ENSESTG00000007370 ENSESTT00000018545 Transcript intron_variant - - - - - - rs5761422 22:26624528 C CCDS54509.1 CCDS54509.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C 23544 NM_001184775.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C CCDS13833.1 CCDS13833.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C 23544 NM_001184777.1 Transcript intron_variant - - - - - - rs5761422 22:26624528 C 23544 NM_001184773.1 Transcript intron_variant - - - - - - rs134981 22:26889450 A - ENSR00000616200 RegulatoryFeature regulatory_region_variant - - - - - - rs134981 22:26889450 A ENSESTG00000012703 ENSESTT00000031937 Transcript intron_variant - - - - - - rs134981 22:26889450 A ENSESTG00000012608 ENSESTT00000031619 Transcript downstream_gene_variant - - - - - - DISTANCE=2417 rs134981 22:26889450 A ENSESTG00000012617 ENSESTT00000031625 Transcript intron_variant - - - - - - rs134981 22:26889450 A CCDS13838.1 CCDS13838.1 Transcript intron_variant - - - - - - rs134981 22:26889450 A 24144 NM_001008697.1 Transcript intron_variant - - - - - - rs134981 22:26889450 A 24144 NM_012143.2 Transcript intron_variant - - - - - - rs134981 22:26889450 A CCDS42995.1 CCDS42995.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1812 rs134981 22:26889450 A 402055 NM_001013694.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1546 rs134981 22:26889450 A ENSESTG00000012703 ENSESTT00000031942 Transcript intron_variant - - - - - - rs4820713 22:27193698 G - - - intergenic_variant - - - - - - rs134165 22:27575769 G - - - intergenic_variant - - - - - - rs134166 22:27606541 G - - - intergenic_variant - - - - - - rs135651 22:28553852 G CCDS46678.1 CCDS46678.1 Transcript intron_variant - - - - - - rs135651 22:28553852 G 23331 NM_001145418.1 Transcript intron_variant - - - - - - rs695475 22:28880821 C CCDS46678.1 CCDS46678.1 Transcript intron_variant - - - - - - rs695475 22:28880821 C 23331 NM_001145418.1 Transcript intron_variant - - - - - - rs4822979 22:29039827 T CCDS46678.1 CCDS46678.1 Transcript intron_variant - - - - - - rs4822979 22:29039827 T ENSESTG00000002992 ENSESTT00000007439 Transcript intron_variant - - - - - - rs4822979 22:29039827 T 23331 NM_001145418.1 Transcript intron_variant - - - - - - rs7510706 22:29125965 C - ENSR00000616536 RegulatoryFeature regulatory_region_variant - - - - - - rs7510706 22:29125965 C 11200 NM_007194.3 Transcript intron_variant - - - - - - rs7510706 22:29125965 C 11200 NM_001257387.1 Transcript intron_variant - - - - - - rs7510706 22:29125965 C CCDS33629.1 CCDS33629.1 Transcript intron_variant - - - - - - rs7510706 22:29125965 C ENSESTG00000002964 ENSESTT00000007426 Transcript intron_variant - - - - - - rs7510706 22:29125965 C CCDS13844.1 CCDS13844.1 Transcript intron_variant - - - - - - rs7510706 22:29125965 C ENSESTG00000002964 ENSESTT00000007427 Transcript intron_variant - - - - - - rs7510706 22:29125965 C 11200 NM_001005735.1 Transcript intron_variant - - - - - - rs7510706 22:29125965 C ENSESTG00000002964 ENSESTT00000007417 Transcript intron_variant - - - - - - rs7510706 22:29125965 C 11200 NM_145862.2 Transcript intron_variant - - - - - - rs7510706 22:29125965 C CCDS13843.1 CCDS13843.1 Transcript intron_variant - - - - - - rs139428 22:29284529 G ENSESTG00000002910 ENSESTT00000007257 Transcript intron_variant - - - - - - rs139428 22:29284529 G 84133 NM_001206998.1 Transcript intron_variant - - - - - - rs139428 22:29284529 G ENSESTG00000002910 ENSESTT00000007267 Transcript intron_variant - - - - - - rs139428 22:29284529 G ENSESTG00000002910 ENSESTT00000007265 Transcript intron_variant - - - - - - rs139428 22:29284529 G CCDS56225.1 CCDS56225.1 Transcript intron_variant - - - - - - rs174763 22:29713045 G CCDS13854.1 CCDS13854.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1810 rs174763 22:29713045 G 10634 NM_152236.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4271 rs174763 22:29713045 G 10634 NM_006478.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4271 rs174763 22:29713045 G 10633 NM_006477.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1300 rs174763 22:29713045 G 10634 NM_152237.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4271 rs2857465 22:29727886 C CCDS13856.2 CCDS13856.2 Transcript missense_variant 2308 2308 770 T/A Acc/Gcc - PolyPhen=benign;SIFT=tolerated rs2857465 22:29727886 C 100500833 NR_037426.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1261 rs2857465 22:29727886 C 162 NM_001166019.1 Transcript missense_variant 2435 2248 750 T/A Acc/Gcc - PolyPhen=benign;SIFT=tolerated rs2857465 22:29727886 C 100113380 NR_003686.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1266 rs2857465 22:29727886 C CCDS54515.1 CCDS54515.1 Transcript missense_variant 2248 2248 750 T/A Acc/Gcc - PolyPhen=benign;SIFT=tolerated rs2857465 22:29727886 C 162 NM_001127.3 Transcript missense_variant 2516 2329 777 T/A Acc/Gcc - PolyPhen=benign;SIFT=tolerated rs2857465 22:29727886 C CCDS13855.1 CCDS13855.1 Transcript missense_variant 2329 2329 777 T/A Acc/Gcc - PolyPhen=benign;SIFT=tolerated rs2857465 22:29727886 C 162 NM_145730.2 Transcript missense_variant 2495 2308 770 T/A Acc/Gcc - PolyPhen=benign;SIFT=tolerated rs1986334 22:29812091 C ENSESTG00000031450 ENSESTT00000079372 Transcript intron_variant - - - - - - rs4820909 22:31266777 C 23762 NM_030758.3 Transcript intron_variant - - - - - - rs4820909 22:31266777 C ENSESTG00000026453 ENSESTT00000066718 Transcript intron_variant - - - - - - rs4820909 22:31266777 C ENSESTG00000026453 ENSESTT00000066677 Transcript downstream_gene_variant - - - - - - DISTANCE=107 rs4820909 22:31266777 C ENSESTG00000026453 ENSESTT00000066662 Transcript intron_variant - - - - - - rs4820909 22:31266777 C ENSESTG00000026453 ENSESTT00000066708 Transcript intron_variant - - - - - - rs4820909 22:31266777 C ENSESTG00000026453 ENSESTT00000066694 Transcript intron_variant - - - - - - rs4820909 22:31266777 C CCDS43002.1 CCDS43002.1 Transcript intron_variant - - - - - - rs715485 22:31607945 A - ENSR00000085075 RegulatoryFeature regulatory_region_variant - - - - - - rs715485 22:31607945 A CCDS13891.1 CCDS13891.1 Transcript upstream_gene_variant - - - - - - DISTANCE=450 rs715485 22:31607945 A ENSESTG00000001696 ENSESTT00000004187 Transcript intron_variant - - - - - - rs715485 22:31607945 A ENSESTG00000001696 ENSESTT00000004166 Transcript intron_variant - - - - - - rs715485 22:31607945 A 91445 NR_024209.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4940 rs715485 22:31607945 A ENSESTG00000001696 ENSESTT00000004220 Transcript upstream_gene_variant - - - - - - DISTANCE=304 rs715485 22:31607945 A ENSESTG00000001673 ENSESTT00000004070 Transcript downstream_gene_variant - - - - - - DISTANCE=4947 rs715485 22:31607945 A 91445 NR_024211.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4940 rs715485 22:31607945 A 91445 NR_024210.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4940 rs715485 22:31607945 A ENSESTG00000001696 ENSESTT00000004225 Transcript upstream_gene_variant - - - - - - DISTANCE=304 rs715485 22:31607945 A 91445 NR_024212.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4940 rs715485 22:31607945 A 91445 NM_152267.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4940 rs715485 22:31607945 A ENSESTG00000001696 ENSESTT00000004182 Transcript intron_variant - - - - - - rs715485 22:31607945 A ENSESTG00000001696 ENSESTT00000004221 Transcript upstream_gene_variant - - - - - - DISTANCE=304 rs715485 22:31607945 A 3985 NM_005569.3 Transcript upstream_gene_variant - - - - - - DISTANCE=305 rs715485 22:31607945 A 91445 NM_001135825.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4940 rs5753520 22:31637828 T CCDS13891.1 CCDS13891.1 Transcript intron_variant - - - - - - rs5753520 22:31637828 T ENSESTG00000001696 ENSESTT00000004187 Transcript intron_variant - - - - - - rs5753520 22:31637828 T ENSESTG00000001696 ENSESTT00000004166 Transcript intron_variant - - - - - - rs5753520 22:31637828 T ENSESTG00000001696 ENSESTT00000004232 Transcript intron_variant - - - - - - rs5753520 22:31637828 T ENSESTG00000001696 ENSESTT00000004220 Transcript intron_variant - - - - - - rs5753520 22:31637828 T ENSESTG00000001696 ENSESTT00000004234 Transcript intron_variant - - - - - - rs5753520 22:31637828 T ENSESTG00000001696 ENSESTT00000004225 Transcript intron_variant - - - - - - rs5753520 22:31637828 T ENSESTG00000001696 ENSESTT00000004182 Transcript intron_variant - - - - - - rs5753520 22:31637828 T ENSESTG00000001696 ENSESTT00000004221 Transcript intron_variant - - - - - - rs5753520 22:31637828 T ENSESTG00000001696 ENSESTT00000004230 Transcript intron_variant - - - - - - rs5753520 22:31637828 T 3985 NM_005569.3 Transcript intron_variant - - - - - - rs5998186 22:32340188 C - ENSR00001532269 RegulatoryFeature regulatory_region_variant - - - - - - rs5998186 22:32340188 C 7533 NM_003405.3 Transcript upstream_gene_variant - - - - - - DISTANCE=291 rs5998186 22:32340188 C ENSESTG00000002393 ENSESTT00000005942 Transcript upstream_gene_variant - - - - - - DISTANCE=332 rs5998186 22:32340188 C CCDS13901.1 CCDS13901.1 Transcript upstream_gene_variant - - - - - - DISTANCE=532 rs5998186 22:32340188 C 25775 NM_015372.1 Transcript intron_variant - - - - - - rs5998186 22:32340188 C ENSESTG00000002402 ENSESTT00000005972 Transcript upstream_gene_variant - - - - - - DISTANCE=794 rs5998186 22:32340188 C ENSESTG00000002433 ENSESTT00000006024 Transcript intron_variant - - - - - - rs5749348 22:32401532 G - ENSR00001532271 RegulatoryFeature regulatory_region_variant - - - - - - rs5749348 22:32401532 G - - - intergenic_variant - - - - - - rs2142719 22:32873181 T CCDS58806.1 CCDS58806.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2007 rs2142719 22:32873181 T 25793 NM_001033024.1 Transcript intron_variant - - - - - - rs2142719 22:32873181 T 25793 NM_012179.3 Transcript intron_variant - - - - - - rs2142719 22:32873181 T ENSESTG00000022169 ENSESTT00000056072 Transcript intron_variant - - - - - - rs2142719 22:32873181 T ENSESTG00000022169 ENSESTT00000055853 Transcript intron_variant - - - - - - rs2142719 22:32873181 T 25793 NM_001257990.1 Transcript intron_variant - - - - - - rs2142719 22:32873181 T CCDS13907.1 CCDS13907.1 Transcript intron_variant - - - - - - rs2142719 22:32873181 T ENSESTG00000022169 ENSESTT00000056005 Transcript intron_variant - - - - - - rs2142719 22:32873181 T CCDS46695.1 CCDS46695.1 Transcript intron_variant - - - - - - rs2142719 22:32873181 T ENSESTG00000022169 ENSESTT00000056023 Transcript intron_variant - - - - - - rs2142719 22:32873181 T ENSESTG00000022169 ENSESTT00000056094 Transcript intron_variant - - - - - - rs2020206 22:32959653 C CCDS13908.1 CCDS13908.1 Transcript intron_variant - - - - - - rs2020206 22:32959653 C 8224 NM_001135774.1 Transcript intron_variant - - - - - - rs2020206 22:32959653 C 8224 NM_133633.2 Transcript intron_variant - - - - - - rs2020206 22:32959653 C 8224 NM_003490.3 Transcript intron_variant - - - - - - rs107615 22:33227080 G - ENSR00000617258 RegulatoryFeature regulatory_region_variant - - - - - - rs107615 22:33227080 G ENSESTG00000022459 ENSESTT00000056710 Transcript downstream_gene_variant - - - - - - DISTANCE=242 rs107615 22:33227080 G ENSESTG00000022421 ENSESTT00000056675 Transcript intron_variant - - - - - - rs107615 22:33227080 G 8224 NM_003490.3 Transcript intron_variant - - - - - - rs107615 22:33227080 G CCDS13908.1 CCDS13908.1 Transcript intron_variant - - - - - - rs107615 22:33227080 G ENSESTG00000022509 ENSESTT00000056830 Transcript intron_variant - - - - - - rs107615 22:33227080 G CCDS13911.1 CCDS13911.1 Transcript intron_variant - - - - - - rs107615 22:33227080 G 7078 NM_000362.4 Transcript intron_variant - - - - - - rs107615 22:33227080 G 8224 NM_133633.2 Transcript intron_variant - - - - - - rs107615 22:33227080 G 8224 NM_001135774.1 Transcript intron_variant - - - - - - rs2899197 22:33451124 T ENSESTG00000022470 ENSESTT00000056771 Transcript intron_variant - - - - - - rs2899197 22:33451124 T 8224 NM_001135774.1 Transcript intron_variant - - - - - - rs987641 22:33559677 G ENSESTG00000015527 ENSESTT00000038889 Transcript upstream_gene_variant - - - - - - DISTANCE=22 rs137360 22:33574954 C - - - intergenic_variant - - - - - - rs130251 22:33730453 G ENSESTG00000015571 ENSESTT00000039093 Transcript intron_variant - - - - - - rs130251 22:33730453 G ENSESTG00000015571 ENSESTT00000039039 Transcript intron_variant - - - - - - rs130251 22:33730453 G ENSESTG00000015571 ENSESTT00000039098 Transcript intron_variant - - - - - - rs130251 22:33730453 G 9215 NM_004737.4 Transcript intron_variant - - - - - - rs130251 22:33730453 G ENSESTG00000015571 ENSESTT00000039108 Transcript intron_variant - - - - - - rs130251 22:33730453 G CCDS13912.1 CCDS13912.1 Transcript intron_variant - - - - - - rs130251 22:33730453 G ENSESTG00000015571 ENSESTT00000039080 Transcript intron_variant - - - - - - rs130251 22:33730453 G ENSESTG00000015571 ENSESTT00000039067 Transcript intron_variant - - - - - - rs130251 22:33730453 G 9215 NM_133642.3 Transcript intron_variant - - - - - - rs130251 22:33730453 G ENSESTG00000015571 ENSESTT00000039050 Transcript intron_variant - - - - - - rs130251 22:33730453 G ENSESTG00000015571 ENSESTT00000039094 Transcript intron_variant - - - - - - rs7290283 22:33848558 G ENSESTG00000015571 ENSESTT00000039093 Transcript intron_variant - - - - - - rs7290283 22:33848558 G ENSESTG00000015571 ENSESTT00000039039 Transcript intron_variant - - - - - - rs7290283 22:33848558 G ENSESTG00000015571 ENSESTT00000039098 Transcript intron_variant - - - - - - rs7290283 22:33848558 G 9215 NM_004737.4 Transcript intron_variant - - - - - - rs7290283 22:33848558 G ENSESTG00000015571 ENSESTT00000039108 Transcript intron_variant - - - - - - rs7290283 22:33848558 G CCDS13912.1 CCDS13912.1 Transcript intron_variant - - - - - - rs7290283 22:33848558 G ENSESTG00000015571 ENSESTT00000039080 Transcript intron_variant - - - - - - rs7290283 22:33848558 G ENSESTG00000015571 ENSESTT00000039067 Transcript intron_variant - - - - - - rs7290283 22:33848558 G 9215 NM_133642.3 Transcript intron_variant - - - - - - rs7290283 22:33848558 G ENSESTG00000015571 ENSESTT00000039050 Transcript intron_variant - - - - - - rs7290283 22:33848558 G ENSESTG00000015571 ENSESTT00000039094 Transcript intron_variant - - - - - - rs5754607 22:33949117 T ENSESTG00000015571 ENSESTT00000039093 Transcript intron_variant - - - - - - rs5754607 22:33949117 T ENSESTG00000015571 ENSESTT00000039039 Transcript intron_variant - - - - - - rs5754607 22:33949117 T ENSESTG00000015571 ENSESTT00000039098 Transcript intron_variant - - - - - - rs5754607 22:33949117 T 9215 NM_004737.4 Transcript intron_variant - - - - - - rs5754607 22:33949117 T ENSESTG00000015571 ENSESTT00000039108 Transcript intron_variant - - - - - - rs5754607 22:33949117 T CCDS13912.1 CCDS13912.1 Transcript intron_variant - - - - - - rs5754607 22:33949117 T ENSESTG00000015571 ENSESTT00000039080 Transcript intron_variant - - - - - - rs5754607 22:33949117 T ENSESTG00000015571 ENSESTT00000039067 Transcript intron_variant - - - - - - rs5754607 22:33949117 T 9215 NM_133642.3 Transcript intron_variant - - - - - - rs5754607 22:33949117 T ENSESTG00000015571 ENSESTT00000039050 Transcript intron_variant - - - - - - rs5754607 22:33949117 T ENSESTG00000015571 ENSESTT00000039094 Transcript intron_variant - - - - - - rs5749636 22:33990896 G ENSESTG00000015571 ENSESTT00000039093 Transcript intron_variant - - - - - - rs5749636 22:33990896 G ENSESTG00000015571 ENSESTT00000039039 Transcript intron_variant - - - - - - rs5749636 22:33990896 G ENSESTG00000015571 ENSESTT00000039098 Transcript intron_variant - - - - - - rs5749636 22:33990896 G 9215 NM_004737.4 Transcript intron_variant - - - - - - rs5749636 22:33990896 G CCDS13912.1 CCDS13912.1 Transcript intron_variant - - - - - - rs5749636 22:33990896 G ENSESTG00000015571 ENSESTT00000039080 Transcript intron_variant - - - - - - rs5749636 22:33990896 G ENSESTG00000015571 ENSESTT00000039067 Transcript intron_variant - - - - - - rs5749636 22:33990896 G 9215 NM_133642.3 Transcript intron_variant - - - - - - rs5749636 22:33990896 G ENSESTG00000015571 ENSESTT00000039050 Transcript intron_variant - - - - - - rs5749636 22:33990896 G ENSESTG00000015571 ENSESTT00000039094 Transcript intron_variant - - - - - - rs240360 22:34070849 T ENSESTG00000015571 ENSESTT00000039093 Transcript intron_variant - - - - - - rs240360 22:34070849 T ENSESTG00000015571 ENSESTT00000039039 Transcript intron_variant - - - - - - rs240360 22:34070849 T ENSESTG00000015571 ENSESTT00000039098 Transcript intron_variant - - - - - - rs240360 22:34070849 T 9215 NM_004737.4 Transcript intron_variant - - - - - - rs240360 22:34070849 T CCDS13912.1 CCDS13912.1 Transcript intron_variant - - - - - - rs240360 22:34070849 T ENSESTG00000015571 ENSESTT00000039080 Transcript intron_variant - - - - - - rs240360 22:34070849 T ENSESTG00000015571 ENSESTT00000039067 Transcript intron_variant - - - - - - rs240360 22:34070849 T 9215 NM_133642.3 Transcript intron_variant - - - - - - rs240360 22:34070849 T ENSESTG00000015571 ENSESTT00000039050 Transcript intron_variant - - - - - - rs240360 22:34070849 T ENSESTG00000015571 ENSESTT00000039094 Transcript intron_variant - - - - - - rs4821174 22:34079082 A ENSESTG00000015571 ENSESTT00000039093 Transcript intron_variant - - - - - - rs4821174 22:34079082 A ENSESTG00000015571 ENSESTT00000039039 Transcript intron_variant - - - - - - rs4821174 22:34079082 A ENSESTG00000015571 ENSESTT00000039098 Transcript intron_variant - - - - - - rs4821174 22:34079082 A 9215 NM_004737.4 Transcript intron_variant - - - - - - rs4821174 22:34079082 A CCDS13912.1 CCDS13912.1 Transcript intron_variant - - - - - - rs4821174 22:34079082 A ENSESTG00000015571 ENSESTT00000039080 Transcript intron_variant - - - - - - rs4821174 22:34079082 A ENSESTG00000015571 ENSESTT00000039067 Transcript intron_variant - - - - - - rs4821174 22:34079082 A 9215 NM_133642.3 Transcript intron_variant - - - - - - rs4821174 22:34079082 A ENSESTG00000015571 ENSESTT00000039050 Transcript intron_variant - - - - - - rs4821174 22:34079082 A ENSESTG00000015571 ENSESTT00000039094 Transcript intron_variant - - - - - - rs130502 22:34338321 A - - - intergenic_variant - - - - - - rs378036 22:34356037 T - - - intergenic_variant - - - - - - rs242900 22:34441581 A ENSESTG00000015555 ENSESTT00000038960 Transcript intron_variant - - - - - - rs5749751 22:34572615 G - - - intergenic_variant - - - - - - rs189944 22:34636027 T - - - intergenic_variant - - - - - - rs130571 22:34854348 C - - - intergenic_variant - - - - - - rs130574 22:34858674 C - - - intergenic_variant - - - - - - rs135160 22:34859742 A - - - intergenic_variant - - - - - - rs137231 22:35066377 T - - - intergenic_variant - - - - - - rs713877 22:35129284 C - - - intergenic_variant - - - - - - rs5755453 22:35350142 C - - - intergenic_variant - - - - - - rs5755454 22:35350227 C - - - intergenic_variant - - - - - - rs1573676 22:35379470 C - - - intergenic_variant - - - - - - rs138782 22:35716131 C 10043 NM_001135730.1 Transcript intron_variant - - - - - - rs138782 22:35716131 C 10043 NM_001135732.1 Transcript intron_variant - - - - - - rs138782 22:35716131 C 10043 NM_005488.2 Transcript intron_variant - - - - - - rs138782 22:35716131 C 10043 NR_024195.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs138782 22:35716131 C ENSESTG00000023731 ENSESTT00000060102 Transcript intron_variant - - - - - - rs138782 22:35716131 C CCDS46697.1 CCDS46697.1 Transcript intron_variant - - - - - - rs138782 22:35716131 C 10043 NR_024194.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs138782 22:35716131 C CCDS13913.1 CCDS13913.1 Transcript intron_variant - - - - - - rs138782 22:35716131 C CCDS46696.1 CCDS46696.1 Transcript intron_variant - - - - - - rs138782 22:35716131 C ENSESTG00000023731 ENSESTT00000060150 Transcript intron_variant - - - - - - rs138782 22:35716131 C 10043 NM_001135729.1 Transcript intron_variant - - - - - - rs138782 22:35716131 C CCDS46698.1 CCDS46698.1 Transcript intron_variant - - - - - - rs138782 22:35716131 C ENSESTG00000023731 ENSESTT00000060055 Transcript intron_variant - - - - - - rs138782 22:35716131 C ENSESTG00000023731 ENSESTT00000060068 Transcript intron_variant - - - - - - rs5755779 22:35993019 G - - - intergenic_variant - - - - - - rs5755970 22:36261692 C 23543 NM_001082578.1 Transcript intron_variant - - - - - - rs5755970 22:36261692 C CCDS43013.1 CCDS43013.1 Transcript intron_variant - - - - - - rs5755970 22:36261692 C ENSESTG00000024218 ENSESTT00000061466 Transcript intron_variant - - - - - - rs5755970 22:36261692 C ENSESTG00000024218 ENSESTT00000061286 Transcript intron_variant - - - - - - rs5755970 22:36261692 C ENSESTG00000024218 ENSESTT00000061538 Transcript intron_variant - - - - - - rs5755970 22:36261692 C ENSESTG00000024218 ENSESTT00000061455 Transcript intron_variant - - - - - - rs5755970 22:36261692 C 23543 NM_001082579.1 Transcript intron_variant - - - - - - rs5755970 22:36261692 C ENSESTG00000024218 ENSESTT00000061512 Transcript intron_variant - - - - - - rs4821452 22:36302005 G 23543 NM_001082578.1 Transcript intron_variant - - - - - - rs4821452 22:36302005 G CCDS43013.1 CCDS43013.1 Transcript intron_variant - - - - - - rs4821452 22:36302005 G ENSESTG00000024218 ENSESTT00000061466 Transcript intron_variant - - - - - - rs4821452 22:36302005 G ENSESTG00000024218 ENSESTT00000061286 Transcript intron_variant - - - - - - rs4821452 22:36302005 G ENSESTG00000024218 ENSESTT00000061538 Transcript intron_variant - - - - - - rs4821452 22:36302005 G ENSESTG00000024218 ENSESTT00000061455 Transcript intron_variant - - - - - - rs4821452 22:36302005 G 23543 NM_001082579.1 Transcript intron_variant - - - - - - rs4821452 22:36302005 G ENSESTG00000024218 ENSESTT00000061512 Transcript intron_variant - - - - - - rs5756073 22:36461517 C - ENSR00000293521 RegulatoryFeature regulatory_region_variant - - - - - - rs5756073 22:36461517 C - - - intergenic_variant - - - - - - rs132760 22:36623731 C ENSESTG00000031930 ENSESTT00000080657 Transcript downstream_gene_variant - - - - - - DISTANCE=328 rs132760 22:36623731 C 23780 NM_030882.2 Transcript missense_variant 1069 733 245 I/V Atc/Gtc - PolyPhen=benign;SIFT=tolerated rs132760 22:36623731 C ENSESTG00000031930 ENSESTT00000080638 Transcript downstream_gene_variant - - - - - - DISTANCE=553 rs132760 22:36623731 C 23780 NM_145637.1 Transcript missense_variant 1210 733 245 I/V Atc/Gtc - PolyPhen=benign;SIFT=tolerated rs132760 22:36623731 C ENSESTG00000031930 ENSESTT00000080620 Transcript downstream_gene_variant - - - - - - DISTANCE=459 rs132760 22:36623731 C CCDS43014.1 CCDS43014.1 Transcript missense_variant 733 733 245 I/V Atc/Gtc - PolyPhen=benign;SIFT=tolerated rs132760 22:36623731 C ENSESTG00000031930 ENSESTT00000080606 Transcript downstream_gene_variant - - - - - - DISTANCE=456 rs132760 22:36623731 C ENSESTG00000031930 ENSESTT00000080631 Transcript downstream_gene_variant - - - - - - DISTANCE=534 rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080339 Transcript intron_variant - - - - - - rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080528 Transcript upstream_gene_variant - - - - - - DISTANCE=908 rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080358 Transcript intron_variant - - - - - - rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080543 Transcript upstream_gene_variant - - - - - - DISTANCE=1263 rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080552 Transcript upstream_gene_variant - - - - - - DISTANCE=1898 rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080538 Transcript upstream_gene_variant - - - - - - DISTANCE=979 rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080509 Transcript intron_variant - - - - - - rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080474 Transcript intron_variant - - - - - - rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080489 Transcript intron_variant - - - - - - rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080397 Transcript intron_variant - - - - - - rs4821477 22:36686239 C CCDS13927.1 CCDS13927.1 Transcript intron_variant - - - - - - rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080208 Transcript intron_variant - - - - - - rs4821477 22:36686239 C ENSESTG00000031724 ENSESTT00000080500 Transcript intron_variant - - - - - - rs4821477 22:36686239 C 4627 NM_002473.4 Transcript intron_variant - - - - - - rs1009151 22:36705052 G ENSESTG00000031724 ENSESTT00000080339 Transcript intron_variant - - - - - - rs1009151 22:36705052 G ENSESTG00000031724 ENSESTT00000080351 Transcript intron_variant - - - - - - rs1009151 22:36705052 G ENSESTG00000031724 ENSESTT00000080358 Transcript intron_variant - - - - - - rs1009151 22:36705052 G ENSESTG00000031724 ENSESTT00000080317 Transcript intron_variant - - - - - - rs1009151 22:36705052 G ENSESTG00000031724 ENSESTT00000080419 Transcript intron_variant - - - - - - rs1009151 22:36705052 G ENSESTG00000031724 ENSESTT00000080397 Transcript intron_variant - - - - - - rs1009151 22:36705052 G CCDS13927.1 CCDS13927.1 Transcript intron_variant - - - - - - rs1009151 22:36705052 G ENSESTG00000031724 ENSESTT00000080208 Transcript intron_variant - - - - - - rs1009151 22:36705052 G ENSESTG00000031724 ENSESTT00000080367 Transcript intron_variant - - - - - - rs1009151 22:36705052 G 4627 NM_002473.4 Transcript intron_variant - - - - - - rs929033 22:36732600 G - ENSR00000617709 RegulatoryFeature regulatory_region_variant - - - - - - rs929033 22:36732600 G CCDS13927.1 CCDS13927.1 Transcript intron_variant - - - - - - rs929033 22:36732600 G ENSESTG00000031724 ENSESTT00000080127 Transcript intron_variant - - - - - - rs929033 22:36732600 G ENSESTG00000031724 ENSESTT00000080115 Transcript intron_variant - - - - - - rs929033 22:36732600 G 4627 NM_002473.4 Transcript intron_variant - - - - - - rs739001 22:37159751 C - ENSR00000617824 RegulatoryFeature regulatory_region_variant - - - - - - rs739001 22:37159751 C CCDS54523.1 CCDS54523.1 Transcript intron_variant - - - - - - rs739001 22:37159751 C ENSESTG00000031483 ENSESTT00000079465 Transcript intron_variant - - - - - - rs739001 22:37159751 C 11020 NM_001177701.2 Transcript intron_variant - - - - - - rs739001 22:37159751 C CCDS13932.1 CCDS13932.1 Transcript intron_variant - - - - - - rs739001 22:37159751 C 11020 NM_006860.4 Transcript intron_variant - - - - - - rs739001 22:37159751 C ENSESTG00000031458 ENSESTT00000079413 Transcript downstream_gene_variant - - - - - - DISTANCE=4076 rs739001 22:37159751 C ENSESTG00000031458 ENSESTT00000079400 Transcript downstream_gene_variant - - - - - - DISTANCE=3574 rs131846 22:37339115 G CCDS13936.1 CCDS13936.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4571 rs131846 22:37339115 G 1439 NM_000395.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2634 rs5750351 22:37376979 G - ENSR00001532633 RegulatoryFeature regulatory_region_variant - - - - - - rs5750351 22:37376979 G - - - intergenic_variant - - - - - - rs855795 22:37448373 G - ENSR00000170156 RegulatoryFeature regulatory_region_variant - - - - - - rs855795 22:37448373 G ENSESTG00000031336 ENSESTT00000079132 Transcript intron_variant - - - - - - rs855795 22:37448373 G ENSESTG00000031336 ENSESTT00000079111 Transcript intron_variant - - - - - - rs855795 22:37448373 G ENSESTG00000031378 ENSESTT00000079154 Transcript intron_variant - - - - - - rs855795 22:37448373 G ENSESTG00000031336 ENSESTT00000079074 Transcript intron_variant - - - - - - rs855795 22:37448373 G CCDS13940.2 CCDS13940.2 Transcript intron_variant - - - - - - rs855795 22:37448373 G ENSESTG00000031336 ENSESTT00000079142 Transcript 5_prime_UTR_variant 164 - - - - - rs855795 22:37448373 G ENSESTG00000031336 ENSESTT00000079092 Transcript intron_variant - - - - - - rs855795 22:37448373 G 79734 NM_024681.2 Transcript intron_variant - - - - - - rs136713 22:37557261 C ENSESTG00000005165 ENSESTT00000013136 Transcript intron_variant - - - - - - rs136713 22:37557261 C ENSESTG00000005165 ENSESTT00000013142 Transcript upstream_gene_variant - - - - - - DISTANCE=4853 rs229496 22:37564203 C - ENSR00000617892 RegulatoryFeature regulatory_region_variant - - - - - - rs229496 22:37564203 C ENSESTG00000005165 ENSESTT00000013136 Transcript intron_variant - - - - - - rs5756559 22:37610816 C 6753 NM_001051.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2463 rs136715 22:37669363 G - - - intergenic_variant - - - - - - rs4555456 22:37746834 G ENSESTG00000005127 ENSESTT00000013006 Transcript intron_variant - - - - - - rs129599 22:37767604 C 114794 NM_052906.3 Transcript 3_prime_UTR_variant 4757 - - - - - rs129599 22:37767604 C ENSESTG00000005118 ENSESTT00000012996 Transcript downstream_gene_variant - - - - - - DISTANCE=4141 rs129599 22:37767604 C ENSESTG00000005127 ENSESTT00000013006 Transcript intron_variant - - - - - - rs129599 22:37767604 C ENSESTG00000005118 ENSESTT00000012995 Transcript downstream_gene_variant - - - - - - DISTANCE=4167 rs129599 22:37767604 C ENSESTG00000005125 ENSESTT00000013001 Transcript downstream_gene_variant - - - - - - DISTANCE=3116 rs129599 22:37767604 C ENSESTG00000005118 ENSESTT00000012986 Transcript downstream_gene_variant - - - - - - DISTANCE=4199 rs129599 22:37767604 C ENSESTG00000005118 ENSESTT00000012991 Transcript downstream_gene_variant - - - - - - DISTANCE=4141 rs129599 22:37767604 C CCDS33642.1 CCDS33642.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1508 rs129599 22:37767604 C ENSESTG00000005118 ENSESTT00000012988 Transcript downstream_gene_variant - - - - - - DISTANCE=4199 rs133704 22:37841694 T - - - intergenic_variant - - - - - - rs5756696 22:37888868 C - ENSR00001532664 RegulatoryFeature regulatory_region_variant - - - - - - rs5756696 22:37888868 C ENSESTG00000005012 ENSESTT00000012775 Transcript downstream_gene_variant - - - - - - DISTANCE=2923 rs5756696 22:37888868 C ENSESTG00000005012 ENSESTT00000012767 Transcript downstream_gene_variant - - - - - - DISTANCE=2923 rs5756696 22:37888868 C CCDS13948.1 CCDS13948.1 Transcript intron_variant - - - - - - rs5756696 22:37888868 C ENSESTG00000005012 ENSESTT00000012759 Transcript downstream_gene_variant - - - - - - DISTANCE=2923 rs5756696 22:37888868 C 29775 NM_014550.3 Transcript intron_variant - - - - - - rs4820313 22:38506509 G - ENSR00000618120 RegulatoryFeature regulatory_region_variant - - - - - - rs4820313 22:38506509 G 8398 NM_001199562.1 Transcript downstream_gene_variant - - - - - - DISTANCE=993 rs4820313 22:38506509 G CCDS13967.1 CCDS13967.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1659 rs4820313 22:38506509 G ENSESTG00000029369 ENSESTT00000074343 Transcript downstream_gene_variant - - - - - - DISTANCE=1744 rs4820313 22:38506509 G 8398 NM_003560.2 Transcript downstream_gene_variant - - - - - - DISTANCE=993 rs4820313 22:38506509 G CCDS43018.1 CCDS43018.1 Transcript synonymous_variant 24 24 8 F ttT/ttC - rs4820313 22:38506509 G ENSESTG00000029369 ENSESTT00000074310 Transcript downstream_gene_variant - - - - - - DISTANCE=1744 rs4820313 22:38506509 G ENSESTG00000029369 ENSESTT00000074300 Transcript downstream_gene_variant - - - - - - DISTANCE=1744 rs4820313 22:38506509 G ENSESTG00000029369 ENSESTT00000074120 Transcript downstream_gene_variant - - - - - - DISTANCE=1744 rs4820313 22:38506509 G ENSESTG00000028057 ENSESTT00000070570 Transcript upstream_gene_variant - - - - - - DISTANCE=1000 rs4820313 22:38506509 G ENSESTG00000029369 ENSESTT00000074337 Transcript downstream_gene_variant - - - - - - DISTANCE=1744 rs4820313 22:38506509 G 80115 NM_025045.4 Transcript synonymous_variant 168 24 8 F ttT/ttC - rs4820313 22:38506509 G ENSESTG00000029369 ENSESTT00000074259 Transcript downstream_gene_variant - - - - - - DISTANCE=1744 rs4820313 22:38506509 G 8398 NM_001004426.1 Transcript downstream_gene_variant - - - - - - DISTANCE=993 rs4820313 22:38506509 G ENSESTG00000029571 ENSESTT00000074509 Transcript synonymous_variant 169 24 8 F ttT/ttC - rs4820313 22:38506509 G CCDS33645.1 CCDS33645.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1659 rs4820313 22:38506509 G ENSESTG00000029369 ENSESTT00000074255 Transcript downstream_gene_variant - - - - - - DISTANCE=1744 rs4820313 22:38506509 G ENSESTG00000029369 ENSESTT00000074136 Transcript downstream_gene_variant - - - - - - DISTANCE=1744 rs4820313 22:38506509 G ENSESTG00000029571 ENSESTT00000074546 Transcript synonymous_variant 143 24 8 F ttT/ttC - rs138404 22:38819296 C - ENSR00000618218 RegulatoryFeature regulatory_region_variant - - - - - - rs138404 22:38819296 C CCDS13971.1 CCDS13971.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3504 rs138404 22:38819296 C ENSESTG00000028092 ENSESTT00000070644 Transcript upstream_gene_variant - - - - - - DISTANCE=997 rs138404 22:38819296 C ENSESTG00000029007 ENSESTT00000073005 Transcript downstream_gene_variant - - - - - - DISTANCE=4374 rs138404 22:38819296 C 3761 NM_004981.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3036 rs138404 22:38819296 C 3761 NM_152868.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3036 rs473879 22:38825169 G CCDS13971.1 CCDS13971.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1032 rs473879 22:38825169 G ENSESTG00000028092 ENSESTT00000070644 Transcript downstream_gene_variant - - - - - - DISTANCE=1161 rs473879 22:38825169 G ENSESTG00000029007 ENSESTT00000073005 Transcript intron_variant - - - - - - rs473879 22:38825169 G 3761 NM_004981.1 Transcript intron_variant - - - - - - rs473879 22:38825169 G 3761 NM_152868.2 Transcript intron_variant - - - - - - rs196089 22:38844879 C ENSESTG00000029007 ENSESTT00000073005 Transcript intron_variant - - - - - - rs196089 22:38844879 C 3761 NM_004981.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4846 rs196089 22:38844879 C 3761 NM_152868.2 Transcript intron_variant - - - - - - rs196090 22:38844911 C ENSESTG00000029007 ENSESTT00000073005 Transcript intron_variant - - - - - - rs196090 22:38844911 C 3761 NM_004981.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4878 rs196090 22:38844911 C 3761 NM_152868.2 Transcript intron_variant - - - - - - rs169032 22:38852905 C ENSESTG00000029007 ENSESTT00000073005 Transcript upstream_gene_variant - - - - - - DISTANCE=1702 rs169032 22:38852905 C 3761 NM_152868.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1700 rs5750638 22:38997248 G ENSESTG00000028825 ENSESTT00000072585 Transcript intron_variant - - - - - - rs5750638 22:38997248 G ENSESTG00000028825 ENSESTT00000072600 Transcript upstream_gene_variant - - - - - - DISTANCE=3957 rs5750638 22:38997248 G ENSESTG00000028773 ENSESTT00000072418 Transcript intron_variant - - - - - - rs5750638 22:38997248 G 646851 NM_001013647.1 Transcript intron_variant - - - - - - rs760646 22:39162655 C - ENSR00001532750 RegulatoryFeature regulatory_region_variant - - - - - - rs760646 22:39162655 C ENSESTG00000028584 ENSESTT00000072145 Transcript intron_variant - - - - - - rs5757364 22:39306377 A - - - intergenic_variant - - - - - - rs760733 22:39329178 A - - - intergenic_variant - - - - - - rs2413563 22:39407979 T ENSESTG00000028489 ENSESTT00000071690 Transcript upstream_gene_variant - - - - - - DISTANCE=2248 rs2413563 22:39407979 T ENSESTG00000027685 ENSESTT00000069743 Transcript intron_variant - - - - - - rs2413563 22:39407979 T 27350 NM_014508.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2286 rs2413563 22:39407979 T ENSESTG00000027685 ENSESTT00000069886 Transcript intron_variant - - - - - - rs2413563 22:39407979 T ENSESTG00000028489 ENSESTT00000071612 Transcript upstream_gene_variant - - - - - - DISTANCE=2218 rs2413563 22:39407979 T ENSESTG00000027685 ENSESTT00000069923 Transcript intron_variant - - - - - - rs2413563 22:39407979 T ENSESTG00000027685 ENSESTT00000069791 Transcript intron_variant - - - - - - rs2413563 22:39407979 T CCDS13983.1 CCDS13983.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2389 rs2413569 22:39464386 C - ENSR00000618318 RegulatoryFeature regulatory_region_variant - - - - - - rs2413569 22:39464386 C ENSESTG00000027685 ENSESTT00000069743 Transcript intron_variant - - - - - - rs2413569 22:39464386 C ENSESTG00000027685 ENSESTT00000069999 Transcript intron_variant - - - - - - rs2413569 22:39464386 C ENSESTG00000027685 ENSESTT00000070012 Transcript intron_variant - - - - - - rs2413569 22:39464386 C ENSESTG00000027685 ENSESTT00000070101 Transcript intron_variant - - - - - - rs2413569 22:39464386 C ENSESTG00000027685 ENSESTT00000069886 Transcript intron_variant - - - - - - rs2413569 22:39464386 C ENSESTG00000027685 ENSESTT00000070034 Transcript intron_variant - - - - - - rs2413569 22:39464386 C ENSESTG00000027685 ENSESTT00000069791 Transcript intron_variant - - - - - - rs2413569 22:39464386 C ENSESTG00000027685 ENSESTT00000070107 Transcript intron_variant - - - - - - rs139276 22:39490726 A 164668 NM_001166002.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2503 rs139276 22:39490726 A 164668 NM_001166003.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2503 rs139276 22:39490726 A 164668 NM_001166004.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2503 rs139276 22:39490726 A ENSESTG00000001884 ENSESTT00000004701 Transcript upstream_gene_variant - - - - - - DISTANCE=2510 rs139276 22:39490726 A 164668 NM_181773.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2503 rs139276 22:39490726 A ENSESTG00000001884 ENSESTT00000004705 Transcript upstream_gene_variant - - - - - - DISTANCE=2550 rs139300 22:39497509 G 164668 NM_001166002.1 Transcript missense_variant,splice_region_variant 545 418 140 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs139300 22:39497509 G 164668 NM_001166003.1 Transcript missense_variant,splice_region_variant 545 418 140 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs139300 22:39497509 G 164668 NM_001166004.1 Transcript missense_variant,splice_region_variant 545 418 140 N/D Aat/Gat - PolyPhen=benign;SIFT=tolerated rs139300 22:39497509 G 164668 NM_181773.3 Transcript missense_variant,splice_region_variant 545 418 140 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs139300 22:39497509 G CCDS54532.1 CCDS54532.1 Transcript missense_variant,splice_region_variant 418 418 140 N/D Aat/Gat - PolyPhen=benign;SIFT=tolerated rs139300 22:39497509 G CCDS13985.1 CCDS13985.1 Transcript missense_variant,splice_region_variant 418 418 140 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs139300 22:39497509 G CCDS54530.1 CCDS54530.1 Transcript missense_variant,splice_region_variant 418 418 140 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs139300 22:39497509 G CCDS54531.1 CCDS54531.1 Transcript missense_variant,splice_region_variant 418 418 140 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs139300 22:39497509 G ENSESTG00000001884 ENSESTT00000004701 Transcript missense_variant,splice_region_variant 538 418 140 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs139300 22:39497509 G ENSESTG00000001884 ENSESTT00000004705 Transcript downstream_gene_variant - - - - - - DISTANCE=970 rs62228489 22:39995284 G 8911 NM_001003406.1 Transcript intron_variant - - - - - - rs62228489 22:39995284 G 8911 NM_021096.3 Transcript intron_variant - - - - - - rs62228489 22:39995284 G CCDS46710.1 CCDS46710.1 Transcript intron_variant - - - - - - rs62228489 22:39995284 G CCDS46711.1 CCDS46711.1 Transcript intron_variant - - - - - - rs5757792 22:40163689 C 150350 NM_152512.3 Transcript intron_variant - - - - - - rs5757792 22:40163689 C ENSESTG00000002112 ENSESTT00000005209 Transcript intron_variant - - - - - - rs5757792 22:40163689 C CCDS13998.1 CCDS13998.1 Transcript intron_variant - - - - - - rs5757792 22:40163689 C ENSESTG00000002112 ENSESTT00000005206 Transcript intron_variant - - - - - - rs6001696 22:40249608 T 150350 NM_152512.3 Transcript intron_variant - - - - - - rs6001696 22:40249608 T ENSESTG00000002112 ENSESTT00000005209 Transcript intron_variant - - - - - - rs6001696 22:40249608 T CCDS13998.1 CCDS13998.1 Transcript intron_variant - - - - - - rs6001696 22:40249608 T ENSESTG00000002112 ENSESTT00000005206 Transcript intron_variant - - - - - - rs137944 22:40266422 G 150350 NM_152512.3 Transcript intron_variant - - - - - - rs137944 22:40266422 G CCDS13998.1 CCDS13998.1 Transcript intron_variant - - - - - - rs137944 22:40266422 G ENSESTG00000002112 ENSESTT00000005194 Transcript intron_variant - - - - - - rs138013 22:40369754 G CCDS13999.1 CCDS13999.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2666 rs138013 22:40369754 G ENSESTG00000002077 ENSESTT00000005123 Transcript downstream_gene_variant - - - - - - DISTANCE=2334 rs138013 22:40369754 G 9402 NM_004810.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2370 rs138013 22:40369754 G ENSESTG00000002077 ENSESTT00000005121 Transcript downstream_gene_variant - - - - - - DISTANCE=2334 rs2213534 22:40427651 G CCDS14000.2 CCDS14000.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2082 rs2213534 22:40427651 G ENSESTG00000002101 ENSESTT00000005162 Transcript upstream_gene_variant - - - - - - DISTANCE=1405 rs2213534 22:40427651 G 100130899 NR_039988.1 Transcript upstream_gene_variant - - - - - - DISTANCE=685 rs2213534 22:40427651 G ENSESTG00000002096 ENSESTT00000005156 Transcript downstream_gene_variant - - - - - - DISTANCE=1819 rs2213534 22:40427651 G 113828 NM_138435.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1608 rs739185 22:40692232 C ENSESTG00000007530 ENSESTT00000019037 Transcript upstream_gene_variant - - - - - - DISTANCE=4628 rs739185 22:40692232 C ENSESTG00000007530 ENSESTT00000018987 Transcript intron_variant - - - - - - rs739185 22:40692232 C 23112 NM_001024843.1 Transcript intron_variant - - - - - - rs739185 22:40692232 C ENSESTG00000007530 ENSESTT00000018978 Transcript intron_variant - - - - - - rs739185 22:40692232 C CCDS54533.1 CCDS54533.1 Transcript intron_variant - - - - - - rs739185 22:40692232 C CCDS46712.1 CCDS46712.1 Transcript intron_variant - - - - - - rs739185 22:40692232 C 23112 NM_015088.2 Transcript intron_variant - - - - - - rs739185 22:40692232 C CCDS46713.1 CCDS46713.1 Transcript intron_variant - - - - - - rs739185 22:40692232 C 23112 NM_001162501.1 Transcript intron_variant - - - - - - rs739185 22:40692232 C ENSESTG00000007530 ENSESTT00000018976 Transcript intron_variant - - - - - - rs739185 22:40692232 C ENSESTG00000007530 ENSESTT00000019033 Transcript intron_variant - - - - - - rs4821956 22:40925049 C 57591 NM_020831.3 Transcript intron_variant - - - - - - rs4821956 22:40925049 C ENSESTG00000007829 ENSESTT00000019819 Transcript intron_variant - - - - - - rs4821956 22:40925049 C ENSESTG00000007829 ENSESTT00000019817 Transcript intron_variant - - - - - - rs4821956 22:40925049 C ENSESTG00000007829 ENSESTT00000019792 Transcript intron_variant - - - - - - rs4821956 22:40925049 C ENSESTG00000007829 ENSESTT00000019822 Transcript intron_variant - - - - - - rs4821956 22:40925049 C ENSESTG00000007829 ENSESTT00000019814 Transcript intron_variant - - - - - - rs138315 22:41206116 G 100616283 NR_039923.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3771 rs138315 22:41206116 G ENSESTG00000007792 ENSESTT00000019716 Transcript intron_variant - - - - - - rs138315 22:41206116 G ENSESTG00000007792 ENSESTT00000019733 Transcript intron_variant - - - - - - rs138315 22:41206116 G ENSESTG00000007792 ENSESTT00000019745 Transcript intron_variant - - - - - - rs138315 22:41206116 G 10478 NM_006358.2 Transcript intron_variant - - - - - - rs138315 22:41206116 G CCDS14005.1 CCDS14005.1 Transcript intron_variant - - - - - - rs4479527 22:41545611 C ENSESTG00000026542 ENSESTT00000067020 Transcript upstream_gene_variant - - - - - - DISTANCE=329 rs4479527 22:41545611 C CCDS14010.1 CCDS14010.1 Transcript intron_variant - - - - - - rs4479527 22:41545611 C ENSESTG00000026441 ENSESTT00000066792 Transcript intron_variant - - - - - - rs4479527 22:41545611 C 2033 NM_001429.3 Transcript intron_variant - - - - - - rs136984 22:42945029 C 253190 NM_014509.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4896 rs136984 22:42945029 C ENSESTG00000020928 ENSESTT00000052683 Transcript intron_variant - - - - - - rs136984 22:42945029 C ENSESTG00000020267 ENSESTT00000051059 Transcript upstream_gene_variant - - - - - - DISTANCE=4895 rs136984 22:42945029 C ENSESTG00000020267 ENSESTT00000050832 Transcript intron_variant - - - - - - rs136984 22:42945029 C CCDS14037.1 CCDS14037.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4998 rs136984 22:42945029 C ENSESTG00000020267 ENSESTT00000050842 Transcript intron_variant - - - - - - rs136984 22:42945029 C ENSESTG00000020267 ENSESTT00000051029 Transcript upstream_gene_variant - - - - - - DISTANCE=4832 rs136984 22:42945029 C ENSESTG00000021007 ENSESTT00000052696 Transcript intron_variant - - - - - - rs136984 22:42945029 C ENSESTG00000020267 ENSESTT00000050869 Transcript upstream_gene_variant - - - - - - DISTANCE=4594 rs136984 22:42945029 C ENSESTG00000020267 ENSESTT00000051016 Transcript upstream_gene_variant - - - - - - DISTANCE=4832 rs136984 22:42945029 C ENSESTG00000020928 ENSESTT00000052609 Transcript intron_variant - - - - - - rs136985 22:42945162 C - ENSR00000618988 RegulatoryFeature regulatory_region_variant - - - - - - rs136985 22:42945162 C 253190 NM_014509.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4763 rs136985 22:42945162 C ENSESTG00000020928 ENSESTT00000052683 Transcript intron_variant - - - - - - rs136985 22:42945162 C ENSESTG00000020267 ENSESTT00000051059 Transcript upstream_gene_variant - - - - - - DISTANCE=4762 rs136985 22:42945162 C ENSESTG00000020267 ENSESTT00000050832 Transcript intron_variant - - - - - - rs136985 22:42945162 C CCDS14037.1 CCDS14037.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4865 rs136985 22:42945162 C ENSESTG00000020267 ENSESTT00000050842 Transcript intron_variant - - - - - - rs136985 22:42945162 C ENSESTG00000020267 ENSESTT00000051029 Transcript upstream_gene_variant - - - - - - DISTANCE=4699 rs136985 22:42945162 C ENSESTG00000021007 ENSESTT00000052696 Transcript intron_variant - - - - - - rs136985 22:42945162 C ENSESTG00000020267 ENSESTT00000050869 Transcript upstream_gene_variant - - - - - - DISTANCE=4461 rs136985 22:42945162 C ENSESTG00000020267 ENSESTT00000051016 Transcript upstream_gene_variant - - - - - - DISTANCE=4699 rs136985 22:42945162 C ENSESTG00000020928 ENSESTT00000052609 Transcript intron_variant - - - - - - rs137057 22:42970515 C CCDS14037.1 CCDS14037.1 Transcript downstream_gene_variant - - - - - - DISTANCE=454 rs137057 22:42970515 C 91695 NR_002184.2 Transcript non_coding_exon_variant,nc_transcript_variant 1067 - - - - - rs137057 22:42970515 C 253190 NM_014509.3 Transcript downstream_gene_variant - - - - - - DISTANCE=127 rs137057 22:42970515 C ENSESTG00000020267 ENSESTT00000051016 Transcript 3_prime_UTR_variant 1565 - - - - - rs137057 22:42970515 C ENSESTG00000020928 ENSESTT00000052683 Transcript intron_variant - - - - - - rs137057 22:42970515 C ENSESTG00000020928 ENSESTT00000052609 Transcript intron_variant - - - - - - rs130398 22:43093784 C - ENSR00000619029 RegulatoryFeature regulatory_region_variant - - - - - - rs130398 22:43093784 C 53947 NM_017436.4 Transcript intron_variant - - - - - - rs130398 22:43093784 C ENSESTG00000020695 ENSESTT00000051893 Transcript intron_variant - - - - - - rs130398 22:43093784 C CCDS14041.1 CCDS14041.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3827 rs130398 22:43093784 C ENSESTG00000020695 ENSESTT00000051935 Transcript intron_variant - - - - - - rs130398 22:43093784 C ENSESTG00000020695 ENSESTT00000051922 Transcript intron_variant - - - - - - rs139019 22:43629408 G ENSESTG00000000854 ENSESTT00000002057 Transcript intron_variant - - - - - - rs139019 22:43629408 G 80274 NM_173050.3 Transcript intron_variant - - - - - - rs139019 22:43629408 G CCDS14048.1 CCDS14048.1 Transcript intron_variant - - - - - - rs139019 22:43629408 G ENSESTG00000001012 ENSESTT00000002447 Transcript intron_variant - - - - - - rs5759276 22:43705563 A 80274 NM_173050.3 Transcript intron_variant - - - - - - rs5759276 22:43705563 A ENSESTG00000001004 ENSESTT00000002429 Transcript intron_variant - - - - - - rs5759276 22:43705563 A CCDS14048.1 CCDS14048.1 Transcript intron_variant - - - - - - rs135061 22:43835302 G CCDS46723.1 CCDS46723.1 Transcript intron_variant - - - - - - rs135061 22:43835302 G ENSESTG00000000860 ENSESTT00000002087 Transcript intron_variant - - - - - - rs135061 22:43835302 G ENSESTG00000000860 ENSESTT00000002099 Transcript intron_variant - - - - - - rs135061 22:43835302 G ENSESTG00000000860 ENSESTT00000002095 Transcript intron_variant - - - - - - rs135061 22:43835302 G 758 NM_001044370.1 Transcript intron_variant - - - - - - rs135061 22:43835302 G ENSESTG00000000860 ENSESTT00000002107 Transcript intron_variant - - - - - - rs146923349 22:43887434 T CCDS46723.1 CCDS46723.1 Transcript intron_variant - - - - - - rs146923349 22:43887434 T ENSESTG00000000860 ENSESTT00000002087 Transcript intron_variant - - - - - - rs146923349 22:43887434 T ENSESTG00000000860 ENSESTT00000002095 Transcript intron_variant - - - - - - rs146923349 22:43887434 T 758 NM_001044370.1 Transcript intron_variant - - - - - - rs146923349 22:43887434 T ENSESTG00000000860 ENSESTT00000002107 Transcript intron_variant - - - - - - rs139886802 22:43896968 A CCDS46723.1 CCDS46723.1 Transcript intron_variant - - - - - - rs139886802 22:43896968 A ENSESTG00000000860 ENSESTT00000002087 Transcript intron_variant - - - - - - rs139886802 22:43896968 A ENSESTG00000000860 ENSESTT00000002095 Transcript intron_variant - - - - - - rs139886802 22:43896968 A 758 NM_001044370.1 Transcript intron_variant - - - - - - rs139886802 22:43896968 A ENSESTG00000000860 ENSESTT00000002116 Transcript upstream_gene_variant - - - - - - DISTANCE=1553 rs139886802 22:43896968 A ENSESTG00000000860 ENSESTT00000002107 Transcript intron_variant - - - - - - rs5764425 22:44354882 T CCDS14055.1 CCDS14055.1 Transcript intron_variant - - - - - - rs5764425 22:44354882 T 25813 NM_015380.4 Transcript intron_variant - - - - - - rs5764425 22:44354882 T ENSESTG00000000891 ENSESTT00000002229 Transcript intron_variant - - - - - - rs130416 22:44422986 G - ENSR00000619258 RegulatoryFeature regulatory_region_variant - - - - - - rs130416 22:44422986 G ENSESTG00000022775 ENSESTT00000057673 Transcript intron_variant - - - - - - rs130416 22:44422986 G ENSESTG00000022775 ENSESTT00000057654 Transcript intron_variant - - - - - - rs130416 22:44422986 G 29780 NM_013327.4 Transcript intron_variant - - - - - - rs130416 22:44422986 G 29780 NM_001243386.1 Transcript intron_variant - - - - - - rs130416 22:44422986 G ENSESTG00000000941 ENSESTT00000002259 Transcript intron_variant - - - - - - rs130416 22:44422986 G CCDS14056.1 CCDS14056.1 Transcript intron_variant - - - - - - rs130416 22:44422986 G ENSESTG00000022775 ENSESTT00000057692 Transcript intron_variant - - - - - - rs130416 22:44422986 G CCDS46724.1 CCDS46724.1 Transcript intron_variant - - - - - - rs130416 22:44422986 G 29780 NM_001003828.2 Transcript intron_variant - - - - - - rs130416 22:44422986 G ENSESTG00000022775 ENSESTT00000057685 Transcript intron_variant - - - - - - rs130315 22:44468217 T ENSESTG00000022775 ENSESTT00000057673 Transcript intron_variant - - - - - - rs130315 22:44468217 T ENSESTG00000022775 ENSESTT00000057654 Transcript intron_variant - - - - - - rs130315 22:44468217 T 29780 NM_013327.4 Transcript intron_variant - - - - - - rs130315 22:44468217 T 29780 NM_001243386.1 Transcript intron_variant - - - - - - rs130315 22:44468217 T 29780 NM_001243385.1 Transcript intron_variant - - - - - - rs130315 22:44468217 T ENSESTG00000000941 ENSESTT00000002259 Transcript intron_variant - - - - - - rs130315 22:44468217 T CCDS58808.1 CCDS58808.1 Transcript intron_variant - - - - - - rs130315 22:44468217 T CCDS14056.1 CCDS14056.1 Transcript intron_variant - - - - - - rs130315 22:44468217 T ENSESTG00000022775 ENSESTT00000057692 Transcript intron_variant - - - - - - rs130315 22:44468217 T CCDS46724.1 CCDS46724.1 Transcript intron_variant - - - - - - rs130315 22:44468217 T 29780 NM_001003828.2 Transcript intron_variant - - - - - - rs130315 22:44468217 T ENSESTG00000022775 ENSESTT00000057685 Transcript intron_variant - - - - - - rs135443 22:44647387 T 85352 NM_001099294.1 Transcript intron_variant - - - - - - rs135443 22:44647387 T ENSESTG00000012149 ENSESTT00000030402 Transcript intron_variant - - - - - - rs135443 22:44647387 T CCDS43025.1 CCDS43025.1 Transcript intron_variant - - - - - - rs135443 22:44647387 T ENSESTG00000023053 ENSESTT00000058173 Transcript downstream_gene_variant - - - - - - DISTANCE=2532 rs135390 22:44680600 C - ENSR00000673587 RegulatoryFeature regulatory_region_variant - - - - - - rs135390 22:44680600 C 85352 NM_001099294.1 Transcript intron_variant - - - - - - rs135390 22:44680600 C ENSESTG00000012149 ENSESTT00000030402 Transcript intron_variant - - - - - - rs135390 22:44680600 C CCDS43025.1 CCDS43025.1 Transcript intron_variant - - - - - - rs6006846 22:45077909 C 55615 NM_001017530.1 Transcript intron_variant - - - - - - rs6006846 22:45077909 C 55615 NM_015366.3 Transcript intron_variant - - - - - - rs6006846 22:45077909 C 55615 NM_001017529.2 Transcript intron_variant - - - - - - rs6006846 22:45077909 C 55615 NM_001198721.1 Transcript intron_variant - - - - - - rs6006846 22:45077909 C ENSESTG00000012054 ENSESTT00000030219 Transcript intron_variant - - - - - - rs6006846 22:45077909 C ENSESTG00000012054 ENSESTT00000030210 Transcript intron_variant - - - - - - rs6006846 22:45077909 C CCDS56232.1 CCDS56232.1 Transcript intron_variant - - - - - - rs6006846 22:45077909 C 55615 NM_001017528.2 Transcript intron_variant - - - - - - rs6006846 22:45077909 C ENSESTG00000012054 ENSESTT00000030213 Transcript downstream_gene_variant - - - - - - DISTANCE=2280 rs6006846 22:45077909 C ENSESTG00000012054 ENSESTT00000030211 Transcript intron_variant - - - - - - rs13055397 22:45081211 C - ENSR00000619368 RegulatoryFeature regulatory_region_variant - - - - - - rs13055397 22:45081211 C 55615 NM_001017530.1 Transcript intron_variant - - - - - - rs13055397 22:45081211 C 55615 NM_015366.3 Transcript intron_variant - - - - - - rs13055397 22:45081211 C 55615 NM_001017529.2 Transcript intron_variant - - - - - - rs13055397 22:45081211 C 55615 NM_001198721.1 Transcript intron_variant - - - - - - rs13055397 22:45081211 C ENSESTG00000012054 ENSESTT00000030210 Transcript intron_variant - - - - - - rs13055397 22:45081211 C ENSESTG00000012054 ENSESTT00000030219 Transcript intron_variant - - - - - - rs13055397 22:45081211 C CCDS56232.1 CCDS56232.1 Transcript intron_variant - - - - - - rs13055397 22:45081211 C 55615 NM_001017528.2 Transcript intron_variant - - - - - - rs13055397 22:45081211 C ENSESTG00000012054 ENSESTT00000030211 Transcript intron_variant - - - - - - rs5766398 22:45477827 G - - - intergenic_variant - - - - - - rs909493 22:45605157 C - ENSR00001042142 RegulatoryFeature regulatory_region_variant - - - - - - rs909493 22:45605157 C CCDS33666.1 CCDS33666.1 Transcript intron_variant - - - - - - rs909493 22:45605157 C 23313 NM_001009880.1 Transcript intron_variant - - - - - - rs909493 22:45605157 C ENSESTG00000002667 ENSESTT00000006658 Transcript intron_variant - - - - - - rs909493 22:45605157 C 23313 NM_015264.1 Transcript intron_variant - - - - - - rs909493 22:45605157 C CCDS33665.1 CCDS33665.1 Transcript intron_variant - - - - - - rs909493 22:45605157 C ENSESTG00000002667 ENSESTT00000006660 Transcript intron_variant - - - - - - rs2742627 22:45680241 G 7380 NM_006953.3 Transcript upstream_gene_variant - - - - - - DISTANCE=627 rs2742627 22:45680241 G 7380 NM_001167574.1 Transcript upstream_gene_variant - - - - - - DISTANCE=627 rs2742627 22:45680241 G CCDS14064.1 CCDS14064.1 Transcript upstream_gene_variant - - - - - - DISTANCE=654 rs2742627 22:45680241 G ENSESTG00000002463 ENSESTT00000006092 Transcript upstream_gene_variant - - - - - - DISTANCE=1628 rs2742627 22:45680241 G CCDS54539.1 CCDS54539.1 Transcript upstream_gene_variant - - - - - - DISTANCE=654 rs226498 22:45702034 T ENSESTG00000002495 ENSESTT00000006179 Transcript upstream_gene_variant - - - - - - DISTANCE=3751 rs226498 22:45702034 T 55007 NM_001104595.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3047 rs226498 22:45702034 T ENSESTG00000002495 ENSESTT00000006176 Transcript upstream_gene_variant - - - - - - DISTANCE=2807 rs226498 22:45702034 T 55007 NM_017911.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3751 rs760549 22:45724855 A - ENSR00001533222 RegulatoryFeature regulatory_region_variant - - - - - - rs760549 22:45724855 A ENSESTG00000002505 ENSESTT00000006199 Transcript upstream_gene_variant - - - - - - DISTANCE=3534 rs760549 22:45724855 A CCDS14065.1 CCDS14065.1 Transcript intron_variant - - - - - - rs760549 22:45724855 A ENSESTG00000002495 ENSESTT00000006179 Transcript downstream_gene_variant - - - - - - DISTANCE=938 rs760549 22:45724855 A 55007 NM_001104595.1 Transcript intron_variant - - - - - - rs760549 22:45724855 A ENSESTG00000002495 ENSESTT00000006176 Transcript downstream_gene_variant - - - - - - DISTANCE=938 rs760549 22:45724855 A 55007 NM_017911.2 Transcript intron_variant - - - - - - rs136603 22:45789642 C 27127 NM_148674.3 Transcript missense_variant 1469 1417 473 F/V Ttt/Gtt - PolyPhen=benign;SIFT=tolerated rs136603 22:45789642 C CCDS43027.1 CCDS43027.1 Transcript missense_variant 1417 1417 473 F/V Ttt/Gtt - PolyPhen=benign;SIFT=tolerated rs4823293 22:45808896 G ENSESTG00000002516 ENSESTT00000006228 Transcript upstream_gene_variant - - - - - - DISTANCE=709 rs4823293 22:45808896 G 27127 NM_148674.3 Transcript intron_variant - - - - - - rs4823293 22:45808896 G 26150 NM_015653.3 Transcript upstream_gene_variant - - - - - - DISTANCE=678 rs4823293 22:45808896 G ENSESTG00000002516 ENSESTT00000006230 Transcript upstream_gene_variant - - - - - - DISTANCE=709 rs4823293 22:45808896 G CCDS43027.1 CCDS43027.1 Transcript intron_variant - - - - - - rs5764739 22:45855381 G - - - intergenic_variant - - - - - - rs134824 22:45986494 C ENSESTG00000002663 ENSESTT00000006636 Transcript intron_variant - - - - - - rs134824 22:45986494 C ENSESTG00000002529 ENSESTT00000006375 Transcript intron_variant - - - - - - rs134824 22:45986494 C 2192 NM_006486.2 Transcript intron_variant - - - - - - rs134824 22:45986494 C ENSESTG00000002529 ENSESTT00000006431 Transcript intron_variant - - - - - - rs134824 22:45986494 C CCDS14067.1 CCDS14067.1 Transcript intron_variant - - - - - - rs138205 22:46162361 A CCDS54540.1 CCDS54540.1 Transcript intron_variant - - - - - - rs138205 22:46162361 A CCDS14070.1 CCDS14070.1 Transcript intron_variant - - - - - - rs138205 22:46162361 A 25814 NM_001167621.1 Transcript intron_variant - - - - - - rs138205 22:46162361 A 25814 NM_013236.3 Transcript intron_variant - - - - - - rs136014 22:46197924 G CCDS54540.1 CCDS54540.1 Transcript intron_variant - - - - - - rs136014 22:46197924 G CCDS14070.1 CCDS14070.1 Transcript intron_variant - - - - - - rs136014 22:46197924 G 25814 NM_001167621.1 Transcript intron_variant - - - - - - rs136014 22:46197924 G ENSESTG00000002637 ENSESTT00000006568 Transcript upstream_gene_variant - - - - - - DISTANCE=4913 rs136014 22:46197924 G 25814 NM_013236.3 Transcript intron_variant - - - - - - rs136014 22:46197924 G ENSESTG00000002637 ENSESTT00000006565 Transcript intron_variant - - - - - - rs8138061 22:46464655 C - ENSR00001533306 RegulatoryFeature regulatory_region_variant - - - - - - rs8138061 22:46464655 C ENSESTG00000031710 ENSESTT00000080057 Transcript intron_variant - - - - - - rs760990 22:46903618 C 9620 NM_014246.1 Transcript intron_variant - - - - - - rs760990 22:46903618 C CCDS14076.1 CCDS14076.1 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081386 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081262 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081222 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081124 Transcript intron_variant - - - - - - rs801655 22:47201712 T CCDS14078.1 CCDS14078.1 Transcript intron_variant - - - - - - rs801655 22:47201712 T 25771 NM_014346.2 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081298 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081320 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081210 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081194 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081219 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081380 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081203 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081255 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081307 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081249 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081350 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081333 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081330 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081313 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081303 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081370 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081324 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081381 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081374 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081244 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081325 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081315 Transcript intron_variant - - - - - - rs801655 22:47201712 T ENSESTG00000032130 ENSESTT00000081263 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081386 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081262 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081222 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081124 Transcript intron_variant - - - - - - rs801654 22:47201777 T CCDS14078.1 CCDS14078.1 Transcript intron_variant - - - - - - rs801654 22:47201777 T 25771 NM_014346.2 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081298 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081320 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081210 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081194 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081219 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081380 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081203 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081255 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081307 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081249 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081350 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081333 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081330 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081313 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081303 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081370 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081324 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081381 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081374 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081244 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081325 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081315 Transcript intron_variant - - - - - - rs801654 22:47201777 T ENSESTG00000032130 ENSESTT00000081263 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081350 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081386 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081124 Transcript intron_variant - - - - - - rs136069 22:47345202 G CCDS14078.1 CCDS14078.1 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081303 Transcript intron_variant - - - - - - rs136069 22:47345202 G 25771 NM_014346.2 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081298 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081320 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081194 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081370 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081324 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081203 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081244 Transcript intron_variant - - - - - - rs136069 22:47345202 G ENSESTG00000032130 ENSESTT00000081249 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081350 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081386 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081124 Transcript intron_variant - - - - - - rs136102 22:47364545 C CCDS14078.1 CCDS14078.1 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081303 Transcript intron_variant - - - - - - rs136102 22:47364545 C 25771 NM_014346.2 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081298 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081320 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081194 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081370 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081324 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081203 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081244 Transcript intron_variant - - - - - - rs136102 22:47364545 C ENSESTG00000032130 ENSESTT00000081249 Transcript intron_variant - - - - - - rs5767506 22:47508248 G ENSESTG00000032130 ENSESTT00000081350 Transcript intron_variant - - - - - - rs5767506 22:47508248 G ENSESTG00000022749 ENSESTT00000057412 Transcript intron_variant - - - - - - rs5767506 22:47508248 G ENSESTG00000022749 ENSESTT00000057418 Transcript intron_variant - - - - - - rs5767506 22:47508248 G ENSESTG00000022749 ENSESTT00000057405 Transcript intron_variant - - - - - - rs5767506 22:47508248 G CCDS14078.1 CCDS14078.1 Transcript intron_variant - - - - - - rs5767506 22:47508248 G 25771 NM_014346.2 Transcript intron_variant - - - - - - rs5767506 22:47508248 G ENSESTG00000032130 ENSESTT00000081298 Transcript intron_variant - - - - - - rs5767506 22:47508248 G ENSESTG00000032130 ENSESTT00000081320 Transcript intron_variant - - - - - - rs5767506 22:47508248 G ENSESTG00000032130 ENSESTT00000081194 Transcript intron_variant - - - - - - rs5767506 22:47508248 G ENSESTG00000032130 ENSESTT00000081244 Transcript intron_variant - - - - - - rs5766703 22:47559903 C - ENSR00000619928 RegulatoryFeature regulatory_region_variant - - - - - - rs5766703 22:47559903 C ENSESTG00000032130 ENSESTT00000081350 Transcript intron_variant - - - - - - rs5766703 22:47559903 C ENSESTG00000022749 ENSESTT00000057412 Transcript intron_variant - - - - - - rs5766703 22:47559903 C ENSESTG00000022749 ENSESTT00000057418 Transcript intron_variant - - - - - - rs5766703 22:47559903 C ENSESTG00000022749 ENSESTT00000057405 Transcript intron_variant - - - - - - rs5766703 22:47559903 C CCDS14078.1 CCDS14078.1 Transcript intron_variant - - - - - - rs5766703 22:47559903 C 25771 NM_014346.2 Transcript intron_variant - - - - - - rs5766703 22:47559903 C ENSESTG00000032130 ENSESTT00000081298 Transcript intron_variant - - - - - - rs5766703 22:47559903 C ENSESTG00000032130 ENSESTT00000081320 Transcript intron_variant - - - - - - rs5766703 22:47559903 C ENSESTG00000032130 ENSESTT00000081194 Transcript intron_variant - - - - - - rs5766703 22:47559903 C ENSESTG00000032130 ENSESTT00000081244 Transcript intron_variant - - - - - - rs6007619 22:47569571 C ENSESTG00000032130 ENSESTT00000081350 Transcript downstream_gene_variant - - - - - - DISTANCE=108 rs6007619 22:47569571 C ENSESTG00000022749 ENSESTT00000057412 Transcript downstream_gene_variant - - - - - - DISTANCE=132 rs6007619 22:47569571 C ENSESTG00000022749 ENSESTT00000057418 Transcript 3_prime_UTR_variant 669 - - - - - rs6007619 22:47569571 C ENSESTG00000022749 ENSESTT00000057405 Transcript downstream_gene_variant - - - - - - DISTANCE=132 rs6007619 22:47569571 C CCDS14078.1 CCDS14078.1 Transcript downstream_gene_variant - - - - - - DISTANCE=302 rs6007619 22:47569571 C 25771 NM_014346.2 Transcript 3_prime_UTR_variant 2022 - - - - - rs6007619 22:47569571 C ENSESTG00000032130 ENSESTT00000081298 Transcript downstream_gene_variant - - - - - - DISTANCE=108 rs6007619 22:47569571 C ENSESTG00000032130 ENSESTT00000081320 Transcript downstream_gene_variant - - - - - - DISTANCE=108 rs6007619 22:47569571 C ENSESTG00000032130 ENSESTT00000081194 Transcript downstream_gene_variant - - - - - - DISTANCE=108 rs6007619 22:47569571 C ENSESTG00000032130 ENSESTT00000081244 Transcript downstream_gene_variant - - - - - - DISTANCE=108 rs738677 22:47611327 A - - - intergenic_variant - - - - - - rs135132 22:47629926 C - - - intergenic_variant - - - - - - rs135133 22:47630056 C - - - intergenic_variant - - - - - - rs131857 22:47778892 C - - - intergenic_variant - - - - - - rs929049 22:47851975 C - - - intergenic_variant - - - - - - rs131054 22:47886156 T ENSESTG00000022822 ENSESTT00000057528 Transcript upstream_gene_variant - - - - - - DISTANCE=3319 rs131054 22:47886156 T ENSESTG00000022822 ENSESTT00000057522 Transcript upstream_gene_variant - - - - - - DISTANCE=3296 rs174085 22:47959616 A - - - intergenic_variant - - - - - - rs174086 22:47980894 T - - - intergenic_variant - - - - - - rs9615181 22:48024612 G ENSESTG00000022799 ENSESTT00000057488 Transcript intron_variant - - - - - - rs9615181 22:48024612 G 400932 NR_033377.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9615181 22:48024612 G ENSESTG00000022784 ENSESTT00000057435 Transcript upstream_gene_variant - - - - - - DISTANCE=2827 rs9615181 22:48024612 G ENSESTG00000022799 ENSESTT00000057502 Transcript upstream_gene_variant - - - - - - DISTANCE=1612 rs135611 22:48540769 A ENSESTG00000025715 ENSESTT00000064833 Transcript upstream_gene_variant - - - - - - DISTANCE=3979 rs135611 22:48540769 A ENSESTG00000025436 ENSESTT00000064166 Transcript downstream_gene_variant - - - - - - DISTANCE=1723 rs133610 22:48683859 G - - - intergenic_variant - - - - - - rs4823746 22:48740452 C - - - intergenic_variant - - - - - - rs113370 22:48791796 G - - - intergenic_variant - - - - - - rs739106 22:48836031 A - - - intergenic_variant - - - - - - rs5771926 22:49065711 C 25817 NM_015381.5 Transcript intron_variant - - - - - - rs5771926 22:49065711 C 25817 NM_001082967.1 Transcript intron_variant - - - - - - rs5771926 22:49065711 C ENSESTG00000025497 ENSESTT00000064288 Transcript intron_variant - - - - - - rs5771926 22:49065711 C ENSESTG00000025497 ENSESTT00000064280 Transcript intron_variant - - - - - - rs5771926 22:49065711 C CCDS46729.1 CCDS46729.1 Transcript intron_variant - - - - - - rs5771926 22:49065711 C ENSESTG00000025497 ENSESTT00000064315 Transcript intron_variant - - - - - - rs5771926 22:49065711 C CCDS46728.1 CCDS46728.1 Transcript intron_variant - - - - - - rs2005640 22:49154175 G ENSESTG00000025497 ENSESTT00000064280 Transcript intron_variant - - - - - - rs5769883 22:49479883 C - - - intergenic_variant - - - - - - rs6009445 22:49489826 A - - - intergenic_variant - - - - - - rs135208 22:49502433 G - - - intergenic_variant - - - - - - rs2688142 22:49638323 T - - - intergenic_variant - - - - - - rs2858633 22:49643045 A - - - intergenic_variant - - - - - - rs2858504 22:49682668 C - - - intergenic_variant - - - - - - rs2688154 22:49714983 T - - - intergenic_variant - - - - - - rs5769628 22:49792549 C - - - intergenic_variant - - - - - - rs6009728 22:49884618 C - - - intergenic_variant - - - - - - rs134476 22:49911152 C - - - intergenic_variant - - - - - - rs5770623 22:50051786 C - ENSR00000171289 RegulatoryFeature regulatory_region_variant - - - - - - rs5770623 22:50051786 C ENSESTG00000029806 ENSESTT00000074962 Transcript intron_variant - - - - - - rs5770623 22:50051786 C ENSESTG00000030074 ENSESTT00000075674 Transcript upstream_gene_variant - - - - - - DISTANCE=854 rs5770623 22:50051786 C 348645 NR_026997.1 Transcript upstream_gene_variant - - - - - - DISTANCE=596 rs5770628 22:50056390 G ENSESTG00000029806 ENSESTT00000074962 Transcript downstream_gene_variant - - - - - - DISTANCE=4108 rs28714287 22:50741145 G ENSESTG00000027152 ENSESTT00000068443 Transcript intron_variant - - - - - - rs28714287 22:50741145 G ENSESTG00000027152 ENSESTT00000068457 Transcript intron_variant - - - - - - rs28714287 22:50741145 G 23654 NM_012401.3 Transcript intron_variant - - - - - - rs6858285 4:56144625 G - - - intergenic_variant - - - - - - rs4864981 4:56219697 G - ENSR00001241464 RegulatoryFeature regulatory_region_variant - - - - - - rs4864981 4:56219697 G ENSESTG00000013085 ENSESTT00000032826 Transcript intron_variant - - - - - - rs4864981 4:56219697 G CCDS3498.1 CCDS3498.1 Transcript intron_variant - - - - - - rs4864981 4:56219697 G 79644 NM_024592.4 Transcript intron_variant - - - - - - rs895616 4:56657182 A - - - intergenic_variant - - - - - - rs1520024 4:57307642 A CCDS47060.1 CCDS47060.1 Transcript intron_variant - - - - - - rs1520024 4:57307642 A ENSESTG00000028925 ENSESTT00000073001 Transcript intron_variant - - - - - - rs1520024 4:57307642 A ENSESTG00000028925 ENSESTT00000072992 Transcript intron_variant - - - - - - rs1520024 4:57307642 A 10606 NM_006452.3 Transcript intron_variant - - - - - - rs1520024 4:57307642 A 10606 NM_001079525.1 Transcript intron_variant - - - - - - rs1520024 4:57307642 A 10606 NM_001079524.1 Transcript intron_variant - - - - - - rs1520024 4:57307642 A ENSESTG00000028925 ENSESTT00000072968 Transcript intron_variant - - - - - - rs1520024 4:57307642 A CCDS47061.1 CCDS47061.1 Transcript intron_variant - - - - - - rs1520024 4:57307642 A ENSESTG00000028925 ENSESTT00000072951 Transcript intron_variant - - - - - - rs4299655 4:57518522 T 84525 NM_001145459.1 Transcript intron_variant - - - - - - rs4299655 4:57518522 T CCDS54767.1 CCDS54767.1 Transcript intron_variant - - - - - - rs4299655 4:57518522 T ENSESTG00000029425 ENSESTT00000074067 Transcript intron_variant - - - - - - rs4299655 4:57518522 T 84525 NM_139212.3 Transcript intron_variant - - - - - - rs4299655 4:57518522 T 84525 NM_139211.4 Transcript intron_variant - - - - - - rs4299655 4:57518522 T ENSESTG00000029425 ENSESTT00000074112 Transcript intron_variant - - - - - - rs4299655 4:57518522 T ENSESTG00000029425 ENSESTT00000074132 Transcript intron_variant - - - - - - rs4299655 4:57518522 T ENSESTG00000029425 ENSESTT00000074087 Transcript intron_variant - - - - - - rs4299655 4:57518522 T ENSESTG00000029425 ENSESTT00000074102 Transcript downstream_gene_variant - - - - - - DISTANCE=3117 rs4299655 4:57518522 T CCDS3507.1 CCDS3507.1 Transcript intron_variant - - - - - - rs4299655 4:57518522 T CCDS47062.1 CCDS47062.1 Transcript intron_variant - - - - - - rs4299655 4:57518522 T 84525 NM_032495.5 Transcript intron_variant - - - - - - rs4299655 4:57518522 T 84525 NM_001145460.1 Transcript intron_variant - - - - - - rs1404383 4:58278140 A - - - intergenic_variant - - - - - - rs6850844 4:59031671 A - - - intergenic_variant - - - - - - rs1433422 4:59072637 G - - - intergenic_variant - - - - - - rs2263554 4:59127143 A - - - intergenic_variant - - - - - - rs2553309 4:59216357 T - - - intergenic_variant - - - - - - rs6554553 4:59579821 T - - - intergenic_variant - - - - - - rs7670447 4:59602500 G - - - intergenic_variant - - - - - - rs11133583 4:59615359 G - - - intergenic_variant - - - - - - rs9990676 4:59693081 T - - - intergenic_variant - - - - - - rs10019767 4:59703408 G - - - intergenic_variant - - - - - - rs1825240 4:60582430 G - - - intergenic_variant - - - - - - rs10019434 4:60950578 A - - - intergenic_variant - - - - - - rs11131216 4:60957507 A - - - intergenic_variant - - - - - - rs4414985 4:61559316 C - - - intergenic_variant - - - - - - rs4412024 4:61988047 C - - - intergenic_variant - - - - - - rs930667 4:62028547 A - - - intergenic_variant - - - - - - rs4860415 4:62289777 G ENSESTG00000021301 ENSESTT00000053513 Transcript intron_variant - - - - - - rs904242 4:62457458 G ENSESTG00000021301 ENSESTT00000053513 Transcript intron_variant - - - - - - rs904242 4:62457458 G 23284 NM_015236.4 Transcript intron_variant - - - - - - rs904242 4:62457458 G CCDS54768.1 CCDS54768.1 Transcript intron_variant - - - - - - rs1353680 4:62476380 T ENSESTG00000021301 ENSESTT00000053513 Transcript intron_variant - - - - - - rs1353680 4:62476380 T 23284 NM_015236.4 Transcript intron_variant - - - - - - rs1353680 4:62476380 T CCDS54768.1 CCDS54768.1 Transcript intron_variant - - - - - - rs7694941 4:62514678 A ENSESTG00000021301 ENSESTT00000053513 Transcript intron_variant - - - - - - rs7694941 4:62514678 A 23284 NM_015236.4 Transcript intron_variant - - - - - - rs7694941 4:62514678 A CCDS54768.1 CCDS54768.1 Transcript intron_variant - - - - - - rs1817051 4:62657652 G 23284 NM_015236.4 Transcript intron_variant - - - - - - rs1817051 4:62657652 G CCDS54768.1 CCDS54768.1 Transcript intron_variant - - - - - - rs7673339 4:62974828 G ENSESTG00000025583 ENSESTT00000064546 Transcript intron_variant - - - - - - rs7673339 4:62974828 G ENSESTG00000025583 ENSESTT00000064583 Transcript intron_variant - - - - - - rs7673339 4:62974828 G ENSESTG00000025583 ENSESTT00000064571 Transcript intron_variant - - - - - - rs7673339 4:62974828 G ENSESTG00000025583 ENSESTT00000064518 Transcript intron_variant - - - - - - rs7673339 4:62974828 G ENSESTG00000025583 ENSESTT00000064593 Transcript intron_variant - - - - - - rs2706033 4:63099538 C - - - intergenic_variant - - - - - - rs13115266 4:63168408 C - - - intergenic_variant - - - - - - rs778564 4:63328622 G - - - intergenic_variant - - - - - - rs4406048 4:63510872 T - - - intergenic_variant - - - - - - rs4860487 4:63741897 T - - - intergenic_variant - - - - - - rs2347812 4:64557750 C - - - intergenic_variant - - - - - - rs4302490 4:64728196 A - - - intergenic_variant - - - - - - rs2167025 4:64863944 T - - - intergenic_variant - - - - - - rs10866146 4:65246236 T ENSESTG00000004729 ENSESTT00000012010 Transcript intron_variant - - - - - - rs10866146 4:65246236 T ENSESTG00000004729 ENSESTT00000012017 Transcript intron_variant - - - - - - rs10866146 4:65246236 T ENSESTG00000004729 ENSESTT00000012013 Transcript intron_variant - - - - - - rs10866146 4:65246236 T ENSESTG00000004729 ENSESTT00000012016 Transcript intron_variant - - - - - - rs10866146 4:65246236 T ENSESTG00000004729 ENSESTT00000012020 Transcript intron_variant - - - - - - rs10866146 4:65246236 T 253017 NM_001010874.4 Transcript intron_variant - - - - - - rs10866146 4:65246236 T CCDS33990.1 CCDS33990.1 Transcript intron_variant - - - - - - rs10866146 4:65246236 T ENSESTG00000004729 ENSESTT00000012015 Transcript intron_variant - - - - - - rs10866146 4:65246236 T ENSESTG00000004729 ENSESTT00000012024 Transcript intron_variant - - - - - - rs3921863 4:65251385 T ENSESTG00000004729 ENSESTT00000012010 Transcript intron_variant - - - - - - rs3921863 4:65251385 T ENSESTG00000004729 ENSESTT00000012017 Transcript intron_variant - - - - - - rs3921863 4:65251385 T ENSESTG00000004729 ENSESTT00000012013 Transcript intron_variant - - - - - - rs3921863 4:65251385 T ENSESTG00000004729 ENSESTT00000012016 Transcript intron_variant - - - - - - rs3921863 4:65251385 T ENSESTG00000004729 ENSESTT00000012020 Transcript intron_variant - - - - - - rs3921863 4:65251385 T 253017 NM_001010874.4 Transcript intron_variant - - - - - - rs3921863 4:65251385 T CCDS33990.1 CCDS33990.1 Transcript intron_variant - - - - - - rs3921863 4:65251385 T ENSESTG00000004729 ENSESTT00000012015 Transcript intron_variant - - - - - - rs3921863 4:65251385 T ENSESTG00000004729 ENSESTT00000012024 Transcript intron_variant - - - - - - rs2714954 4:65380583 T - - - intergenic_variant - - - - - - rs10007458 4:65551440 C - - - intergenic_variant - - - - - - rs6855660 4:65631552 A - - - intergenic_variant - - - - - - rs4443336 4:65855282 T 401134 NR_033976.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4443336 4:65855282 T ENSESTG00000018943 ENSESTT00000047664 Transcript intron_variant - - - - - - rs1978917 4:65965077 T - - - intergenic_variant - - - - - - rs6839586 4:66641840 T - - - intergenic_variant - - - - - - rs338952 4:67090473 A - - - intergenic_variant - - - - - - rs2941864 4:67184735 G - - - intergenic_variant - - - - - - rs1511287 4:67213330 C - - - intergenic_variant - - - - - - rs7672548 4:67657676 A - - - intergenic_variant - - - - - - rs1579714 4:68154144 C - - - intergenic_variant - - - - - - rs356328 4:68231292 A - - - intergenic_variant - - - - - - rs2200592 4:68463810 C ENSESTG00000027832 ENSESTT00000070182 Transcript intron_variant - - - - - - rs2200592 4:68463810 C ENSESTG00000027832 ENSESTT00000070155 Transcript downstream_gene_variant - - - - - - DISTANCE=4801 rs2200592 4:68463810 C 26228 NM_012108.2 Transcript intron_variant - - - - - - rs2200592 4:68463810 C CCDS3515.1 CCDS3515.1 Transcript intron_variant - - - - - - rs2711147 4:68682929 A 9407 NM_004262.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3665 rs1595515 4:68846959 G - - - intergenic_variant - - - - - - rs7681880 4:68855632 A 644759 NR_033737.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1898 rs1438438 4:68913767 G - - - intergenic_variant - - - - - - rs970659 4:68958924 T ENSESTG00000021035 ENSESTT00000052801 Transcript intron_variant - - - - - - rs970659 4:68958924 T CCDS3520.1 CCDS3520.1 Transcript intron_variant - - - - - - rs970659 4:68958924 T 389208 NM_207407.2 Transcript intron_variant - - - - - - rs970659 4:68958924 T ENSESTG00000021035 ENSESTT00000052822 Transcript intron_variant - - - - - - rs7440016 4:69079482 A ENSESTG00000021011 ENSESTT00000052729 Transcript intron_variant - - - - - - rs7440016 4:69079482 A 100130017 NR_015446.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1294 rs7440016 4:69079482 A ENSESTG00000021011 ENSESTT00000052758 Transcript intron_variant - - - - - - rs7440016 4:69079482 A 401136 NM_001129907.2 Transcript intron_variant - - - - - - rs7440016 4:69079482 A CCDS47066.1 CCDS47066.1 Transcript intron_variant - - - - - - rs7667707 4:69153998 A - - - intergenic_variant - - - - - - rs1841053 4:69875383 A - - - intergenic_variant - - - - - - rs7694809 4:70179258 C ENSESTG00000020176 ENSESTT00000050568 Transcript intron_variant - - - - - - rs1826678 4:70308490 A - - - intergenic_variant - - - - - - rs1845555 4:70355211 C CCDS43234.1 CCDS43234.1 Transcript synonymous_variant 948 948 316 T acA/acG - rs1845555 4:70355211 C ENSESTG00000020208 ENSESTT00000050704 Transcript synonymous_variant 982 948 316 T acA/acG - rs1845555 4:70355211 C ENSESTG00000020208 ENSESTT00000050720 Transcript synonymous_variant 730 696 232 T acA/acG - rs1845555 4:70355211 C 7363 NM_021139.2 Transcript synonymous_variant 995 948 316 T acA/acG - rs1845555 4:70355211 C ENSESTG00000020208 ENSESTT00000050717 Transcript synonymous_variant 687 357 119 T acA/acG - rs1845555 4:70355211 C ENSESTG00000020208 ENSESTT00000050677 Transcript synonymous_variant 555 270 90 T acA/acG - rs1432328 4:70358662 G CCDS43234.1 CCDS43234.1 Transcript intron_variant - - - - - - rs1432328 4:70358662 G ENSESTG00000020208 ENSESTT00000050704 Transcript intron_variant - - - - - - rs1432328 4:70358662 G ENSESTG00000020208 ENSESTT00000050720 Transcript intron_variant - - - - - - rs1432328 4:70358662 G ENSESTG00000020208 ENSESTT00000050684 Transcript downstream_gene_variant - - - - - - DISTANCE=2231 rs1432328 4:70358662 G 7363 NM_021139.2 Transcript intron_variant - - - - - - rs1432328 4:70358662 G ENSESTG00000020208 ENSESTT00000050717 Transcript intron_variant - - - - - - rs1432328 4:70358662 G ENSESTG00000020208 ENSESTT00000050677 Transcript intron_variant - - - - - - rs11728785 4:70461271 G 10941 NM_001252275.1 Transcript intron_variant - - - - - - rs11728785 4:70461271 G CCDS58902.1 CCDS58902.1 Transcript intron_variant - - - - - - rs11728785 4:70461271 G 10941 NM_001252274.1 Transcript intron_variant - - - - - - rs11728785 4:70461271 G 574537 NM_001105677.2 Transcript intron_variant - - - - - - rs11728785 4:70461271 G CCDS3529.1 CCDS3529.1 Transcript intron_variant - - - - - - rs11728785 4:70461271 G CCDS56331.1 CCDS56331.1 Transcript intron_variant - - - - - - rs11728785 4:70461271 G CCDS58901.1 CCDS58901.1 Transcript intron_variant - - - - - - rs11728785 4:70461271 G 10941 NM_006798.3 Transcript intron_variant - - - - - - rs4550998 4:70466714 A 10941 NM_001252275.1 Transcript intron_variant - - - - - - rs4550998 4:70466714 A CCDS58902.1 CCDS58902.1 Transcript intron_variant - - - - - - rs4550998 4:70466714 A 10941 NM_001252274.1 Transcript intron_variant - - - - - - rs4550998 4:70466714 A 574537 NM_001105677.2 Transcript intron_variant - - - - - - rs4550998 4:70466714 A CCDS3529.1 CCDS3529.1 Transcript intron_variant - - - - - - rs4550998 4:70466714 A CCDS56331.1 CCDS56331.1 Transcript intron_variant - - - - - - rs4550998 4:70466714 A CCDS58901.1 CCDS58901.1 Transcript intron_variant - - - - - - rs4550998 4:70466714 A 10941 NM_006798.3 Transcript intron_variant - - - - - - rs2033801 4:70482416 A 10941 NM_001252275.1 Transcript intron_variant - - - - - - rs2033801 4:70482416 A CCDS58902.1 CCDS58902.1 Transcript intron_variant - - - - - - rs2033801 4:70482416 A 10941 NM_001252274.1 Transcript intron_variant - - - - - - rs2033801 4:70482416 A 574537 NM_001105677.2 Transcript intron_variant - - - - - - rs2033801 4:70482416 A CCDS3529.1 CCDS3529.1 Transcript intron_variant - - - - - - rs2033801 4:70482416 A CCDS56331.1 CCDS56331.1 Transcript intron_variant - - - - - - rs2033801 4:70482416 A CCDS58901.1 CCDS58901.1 Transcript intron_variant - - - - - - rs2033801 4:70482416 A 10941 NM_006798.3 Transcript intron_variant - - - - - - rs1347046 4:70513139 T CCDS58901.1 CCDS58901.1 Transcript missense_variant 224 224 75 R/K aGg/aAg - PolyPhen=benign;SIFT=tolerated rs1347046 4:70513139 T 10941 NM_001252275.1 Transcript missense_variant 340 224 75 R/K aGg/aAg - PolyPhen=benign;SIFT=tolerated rs1347046 4:70513139 T CCDS58902.1 CCDS58902.1 Transcript missense_variant 224 224 75 R/K aGg/aAg - PolyPhen=benign;SIFT=tolerated rs1347046 4:70513139 T 10941 NM_001252274.1 Transcript missense_variant 340 224 75 R/K aGg/aAg - PolyPhen=benign;SIFT=tolerated rs1347046 4:70513139 T CCDS3529.1 CCDS3529.1 Transcript missense_variant 224 224 75 R/K aGg/aAg - PolyPhen=benign;SIFT=tolerated rs1347046 4:70513139 T 10941 NM_006798.3 Transcript missense_variant 340 224 75 R/K aGg/aAg - PolyPhen=benign;SIFT=tolerated rs1368116 4:70515423 C - ENSR00001431812 RegulatoryFeature regulatory_region_variant - - - - - - rs1368116 4:70515423 C CCDS58901.1 CCDS58901.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2061 rs1368116 4:70515423 C 10941 NM_001252275.1 Transcript intron_variant - - - - - - rs1368116 4:70515423 C CCDS58902.1 CCDS58902.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2061 rs1368116 4:70515423 C 10941 NM_001252274.1 Transcript intron_variant - - - - - - rs1368116 4:70515423 C CCDS3529.1 CCDS3529.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2061 rs1368116 4:70515423 C 10941 NM_006798.3 Transcript intron_variant - - - - - - rs2043241 4:70520821 T 10941 NM_001252275.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1854 rs2043241 4:70520821 T 10941 NM_001252274.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1854 rs2043241 4:70520821 T 10941 NM_006798.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1854 rs7658556 4:70526526 T - - - intergenic_variant - - - - - - rs1237376 4:70786907 T - - - intergenic_variant - - - - - - rs708234 4:71019255 G CCDS3535.1 CCDS3535.1 Transcript upstream_gene_variant - - - - - - DISTANCE=838 rs708234 4:71019255 G 401137 NM_214711.3 Transcript upstream_gene_variant - - - - - - DISTANCE=649 rs1383435 4:71216923 C - - - intergenic_variant - - - - - - rs1387962 4:71345877 T CCDS3541.1 CCDS3541.1 Transcript intron_variant - - - - - - rs1387962 4:71345877 T ENSESTG00000033494 ENSESTT00000084694 Transcript intron_variant - - - - - - rs1387962 4:71345877 T 4589 NM_001145007.1 Transcript intron_variant - - - - - - rs1387962 4:71345877 T 4589 NM_152291.2 Transcript intron_variant - - - - - - rs1387962 4:71345877 T ENSESTG00000033494 ENSESTT00000084700 Transcript intron_variant - - - - - - rs1387962 4:71345877 T 4589 NM_001145006.1 Transcript intron_variant - - - - - - rs28657800 4:71564039 T - - - intergenic_variant - - - - - - rs7662236 4:71682868 C ENSESTG00000001463 ENSESTT00000003507 Transcript downstream_gene_variant - - - - - - DISTANCE=3452 rs7662236 4:71682868 C ENSESTG00000001463 ENSESTT00000003505 Transcript downstream_gene_variant - - - - - - DISTANCE=3452 rs7662236 4:71682868 C 2926 NM_001098477.1 Transcript 3_prime_UTR_variant 5098 - - - - - rs7662236 4:71682868 C ENSESTG00000001463 ENSESTT00000003508 Transcript downstream_gene_variant - - - - - - DISTANCE=3452 rs7662236 4:71682868 C ENSESTG00000001463 ENSESTT00000003498 Transcript downstream_gene_variant - - - - - - DISTANCE=3452 rs7662236 4:71682868 C 2926 NM_002092.3 Transcript 3_prime_UTR_variant 5262 - - - - - rs6847924 4:71759846 T - - - intergenic_variant - - - - - - rs7673241 4:71780093 G - ENSR00001242506 RegulatoryFeature regulatory_region_variant - - - - - - rs7673241 4:71780093 G ENSESTG00000001264 ENSESTT00000002994 Transcript intron_variant - - - - - - rs7673241 4:71780093 G ENSESTG00000001264 ENSESTT00000002999 Transcript intron_variant - - - - - - rs7673241 4:71780093 G 92597 NM_001244766.1 Transcript intron_variant - - - - - - rs7673241 4:71780093 G 92597 NM_001244767.1 Transcript intron_variant - - - - - - rs7673241 4:71780093 G CCDS34002.1 CCDS34002.1 Transcript intron_variant - - - - - - rs7673241 4:71780093 G 92597 NM_173468.3 Transcript intron_variant - - - - - - rs6847068 4:71789494 G ENSESTG00000001264 ENSESTT00000002994 Transcript intron_variant - - - - - - rs6847068 4:71789494 G ENSESTG00000001264 ENSESTT00000002999 Transcript intron_variant - - - - - - rs6847068 4:71789494 G 92597 NM_001244766.1 Transcript intron_variant - - - - - - rs6847068 4:71789494 G 92597 NM_001244767.1 Transcript intron_variant - - - - - - rs6847068 4:71789494 G CCDS34002.1 CCDS34002.1 Transcript intron_variant - - - - - - rs6847068 4:71789494 G 92597 NM_173468.3 Transcript intron_variant - - - - - - rs7667343 4:71796200 A ENSESTG00000001264 ENSESTT00000002994 Transcript intron_variant - - - - - - rs7667343 4:71796200 A ENSESTG00000001264 ENSESTT00000002999 Transcript intron_variant - - - - - - rs7667343 4:71796200 A 92597 NM_001244766.1 Transcript intron_variant - - - - - - rs7667343 4:71796200 A 92597 NM_001244767.1 Transcript intron_variant - - - - - - rs7667343 4:71796200 A CCDS34002.1 CCDS34002.1 Transcript intron_variant - - - - - - rs7667343 4:71796200 A 92597 NM_173468.3 Transcript intron_variant - - - - - - rs4694359 4:71810966 A ENSESTG00000001264 ENSESTT00000002994 Transcript intron_variant - - - - - - rs4694359 4:71810966 A ENSESTG00000001264 ENSESTT00000002999 Transcript intron_variant - - - - - - rs4694359 4:71810966 A 92597 NM_001244766.1 Transcript intron_variant - - - - - - rs4694359 4:71810966 A 92597 NM_001244767.1 Transcript intron_variant - - - - - - rs4694359 4:71810966 A CCDS34002.1 CCDS34002.1 Transcript intron_variant - - - - - - rs4694359 4:71810966 A 92597 NM_173468.3 Transcript intron_variant - - - - - - rs7655362 4:71930978 G - - - intergenic_variant - - - - - - rs1466198 4:72003697 G - - - intergenic_variant - - - - - - rs990554 4:72018054 T - - - intergenic_variant - - - - - - rs4694391 4:72203052 A 8671 NM_001134742.1 Transcript intron_variant - - - - - - rs4694391 4:72203052 A 8671 NM_001098484.2 Transcript intron_variant - - - - - - rs4694391 4:72203052 A CCDS47071.1 CCDS47071.1 Transcript intron_variant - - - - - - rs4694391 4:72203052 A 8671 NM_003759.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1718 rs4694391 4:72203052 A ENSESTG00000001298 ENSESTT00000003103 Transcript upstream_gene_variant - - - - - - DISTANCE=1785 rs4694391 4:72203052 A ENSESTG00000001298 ENSESTT00000003099 Transcript upstream_gene_variant - - - - - - DISTANCE=1692 rs4694391 4:72203052 A ENSESTG00000001298 ENSESTT00000003061 Transcript intron_variant - - - - - - rs4694391 4:72203052 A CCDS3549.1 CCDS3549.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1914 rs4694391 4:72203052 A CCDS43236.1 CCDS43236.1 Transcript intron_variant - - - - - - rs4694391 4:72203052 A ENSESTG00000001298 ENSESTT00000003068 Transcript intron_variant - - - - - - rs4694391 4:72203052 A ENSESTG00000001298 ENSESTT00000003075 Transcript upstream_gene_variant - - - - - - DISTANCE=1692 rs4277753 4:72233708 A 8671 NM_001134742.1 Transcript intron_variant - - - - - - rs4277753 4:72233708 A 8671 NM_001098484.2 Transcript intron_variant - - - - - - rs4277753 4:72233708 A CCDS47071.1 CCDS47071.1 Transcript intron_variant - - - - - - rs4277753 4:72233708 A 8671 NM_003759.3 Transcript intron_variant - - - - - - rs4277753 4:72233708 A ENSESTG00000001298 ENSESTT00000003103 Transcript intron_variant - - - - - - rs4277753 4:72233708 A ENSESTG00000001298 ENSESTT00000003099 Transcript intron_variant - - - - - - rs4277753 4:72233708 A CCDS3549.1 CCDS3549.1 Transcript intron_variant - - - - - - rs4277753 4:72233708 A CCDS43236.1 CCDS43236.1 Transcript intron_variant - - - - - - rs4277753 4:72233708 A ENSESTG00000001298 ENSESTT00000003075 Transcript intron_variant - - - - - - rs4287977 4:72245217 T 8671 NM_001134742.1 Transcript intron_variant - - - - - - rs4287977 4:72245217 T 8671 NM_001098484.2 Transcript intron_variant - - - - - - rs4287977 4:72245217 T CCDS47071.1 CCDS47071.1 Transcript intron_variant - - - - - - rs4287977 4:72245217 T 8671 NM_003759.3 Transcript intron_variant - - - - - - rs4287977 4:72245217 T ENSESTG00000001298 ENSESTT00000003103 Transcript intron_variant - - - - - - rs4287977 4:72245217 T ENSESTG00000001298 ENSESTT00000003099 Transcript intron_variant - - - - - - rs4287977 4:72245217 T CCDS3549.1 CCDS3549.1 Transcript intron_variant - - - - - - rs4287977 4:72245217 T CCDS43236.1 CCDS43236.1 Transcript intron_variant - - - - - - rs4287977 4:72245217 T ENSESTG00000001298 ENSESTT00000003075 Transcript intron_variant - - - - - - rs6847618 4:72247131 C 8671 NM_001134742.1 Transcript intron_variant - - - - - - rs6847618 4:72247131 C 8671 NM_001098484.2 Transcript intron_variant - - - - - - rs6847618 4:72247131 C CCDS47071.1 CCDS47071.1 Transcript intron_variant - - - - - - rs6847618 4:72247131 C 8671 NM_003759.3 Transcript intron_variant - - - - - - rs6847618 4:72247131 C ENSESTG00000001298 ENSESTT00000003103 Transcript intron_variant - - - - - - rs6847618 4:72247131 C ENSESTG00000001298 ENSESTT00000003099 Transcript intron_variant - - - - - - rs6847618 4:72247131 C CCDS3549.1 CCDS3549.1 Transcript intron_variant - - - - - - rs6847618 4:72247131 C CCDS43236.1 CCDS43236.1 Transcript intron_variant - - - - - - rs6847618 4:72247131 C ENSESTG00000001298 ENSESTT00000003075 Transcript intron_variant - - - - - - rs4589998 4:72362405 G 8671 NM_001134742.1 Transcript intron_variant - - - - - - rs4589998 4:72362405 G 8671 NM_001098484.2 Transcript intron_variant - - - - - - rs4589998 4:72362405 G CCDS47071.1 CCDS47071.1 Transcript intron_variant - - - - - - rs4589998 4:72362405 G 8671 NM_003759.3 Transcript intron_variant - - - - - - rs4589998 4:72362405 G ENSESTG00000001298 ENSESTT00000003099 Transcript intron_variant - - - - - - rs4589998 4:72362405 G CCDS3549.1 CCDS3549.1 Transcript intron_variant - - - - - - rs4589998 4:72362405 G CCDS43236.1 CCDS43236.1 Transcript intron_variant - - - - - - rs4589998 4:72362405 G ENSESTG00000001298 ENSESTT00000003075 Transcript intron_variant - - - - - - rs4435714 4:72365283 C 8671 NM_001134742.1 Transcript intron_variant - - - - - - rs4435714 4:72365283 C 8671 NM_001098484.2 Transcript intron_variant - - - - - - rs4435714 4:72365283 C CCDS47071.1 CCDS47071.1 Transcript intron_variant - - - - - - rs4435714 4:72365283 C 8671 NM_003759.3 Transcript intron_variant - - - - - - rs4435714 4:72365283 C ENSESTG00000001298 ENSESTT00000003099 Transcript downstream_gene_variant - - - - - - DISTANCE=2025 rs4435714 4:72365283 C CCDS3549.1 CCDS3549.1 Transcript intron_variant - - - - - - rs4435714 4:72365283 C CCDS43236.1 CCDS43236.1 Transcript intron_variant - - - - - - rs4435714 4:72365283 C ENSESTG00000001298 ENSESTT00000003075 Transcript intron_variant - - - - - - rs7693422 4:72442282 G 8671 NM_001134742.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4478 rs7693422 4:72442282 G 8671 NM_001098484.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4478 rs7693422 4:72442282 G 8671 NM_003759.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4478 rs4694406 4:72458211 G - - - intergenic_variant - - - - - - rs2364550 4:72464514 C - - - intergenic_variant - - - - - - rs450288 4:72560703 T - - - intergenic_variant - - - - - - rs413347 4:72564865 G - - - intergenic_variant - - - - - - rs393538 4:72568501 G - - - intergenic_variant - - - - - - rs371766 4:72575618 A - - - intergenic_variant - - - - - - rs1099024 4:72585408 A - - - intergenic_variant - - - - - - rs2933153 4:72590532 C - - - intergenic_variant - - - - - - rs222052 4:72604606 G 2638 NM_000583.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2804 rs222052 4:72604606 G ENSESTG00000001435 ENSESTT00000003432 Transcript downstream_gene_variant - - - - - - DISTANCE=2807 rs222052 4:72604606 G 2638 NM_001204306.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2804 rs222052 4:72604606 G ENSESTG00000001435 ENSESTT00000003435 Transcript downstream_gene_variant - - - - - - DISTANCE=2806 rs222052 4:72604606 G 2638 NM_001204307.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2804 rs222041 4:72616314 G 2638 NM_000583.3 Transcript intron_variant - - - - - - rs222041 4:72616314 G ENSESTG00000001435 ENSESTT00000003432 Transcript intron_variant - - - - - - rs222041 4:72616314 G 2638 NM_001204306.1 Transcript intron_variant - - - - - - rs222041 4:72616314 G ENSESTG00000001435 ENSESTT00000003435 Transcript intron_variant - - - - - - rs222041 4:72616314 G CCDS56332.1 CCDS56332.1 Transcript intron_variant - - - - - - rs222041 4:72616314 G CCDS3550.1 CCDS3550.1 Transcript intron_variant - - - - - - rs222041 4:72616314 G 2638 NM_001204307.1 Transcript intron_variant - - - - - - rs222034 4:72622208 C 2638 NM_000583.3 Transcript intron_variant - - - - - - rs222034 4:72622208 C ENSESTG00000001435 ENSESTT00000003432 Transcript intron_variant - - - - - - rs222034 4:72622208 C 2638 NM_001204306.1 Transcript intron_variant - - - - - - rs222034 4:72622208 C ENSESTG00000001435 ENSESTT00000003435 Transcript upstream_gene_variant - - - - - - DISTANCE=1397 rs222034 4:72622208 C CCDS56332.1 CCDS56332.1 Transcript intron_variant - - - - - - rs222034 4:72622208 C CCDS3550.1 CCDS3550.1 Transcript intron_variant - - - - - - rs222034 4:72622208 C 2638 NM_001204307.1 Transcript intron_variant - - - - - - rs222022 4:72636698 A 2638 NM_000583.3 Transcript intron_variant - - - - - - rs222022 4:72636698 A 2638 NM_001204306.1 Transcript intron_variant - - - - - - rs222022 4:72636698 A ENSESTG00000001405 ENSESTT00000003334 Transcript intron_variant - - - - - - rs222022 4:72636698 A CCDS3550.1 CCDS3550.1 Transcript intron_variant - - - - - - rs222022 4:72636698 A 2638 NM_001204307.1 Transcript intron_variant - - - - - - rs222022 4:72636698 A CCDS56332.1 CCDS56332.1 Transcript intron_variant - - - - - - rs222022 4:72636698 A ENSESTG00000001405 ENSESTT00000003328 Transcript intron_variant - - - - - - rs222022 4:72636698 A ENSESTG00000001405 ENSESTT00000003340 Transcript intron_variant - - - - - - rs221996 4:72653037 C 2638 NM_000583.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2958 rs221996 4:72653037 C 2638 NM_001204306.1 Transcript intron_variant - - - - - - rs221996 4:72653037 C ENSESTG00000001405 ENSESTT00000003334 Transcript upstream_gene_variant - - - - - - DISTANCE=3261 rs221996 4:72653037 C CCDS3550.1 CCDS3550.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3302 rs221996 4:72653037 C 2638 NM_001204307.1 Transcript intron_variant - - - - - - rs221996 4:72653037 C CCDS56332.1 CCDS56332.1 Transcript intron_variant - - - - - - rs221996 4:72653037 C ENSESTG00000001405 ENSESTT00000003328 Transcript upstream_gene_variant - - - - - - DISTANCE=3241 rs221996 4:72653037 C ENSESTG00000001405 ENSESTT00000003340 Transcript upstream_gene_variant - - - - - - DISTANCE=3271 rs6446773 4:72822294 A - - - intergenic_variant - - - - - - rs6848431 4:72828955 A - - - intergenic_variant - - - - - - rs4694450 4:72902750 C 10886 NM_004885.2 Transcript intron_variant - - - - - - rs4694450 4:72902750 C 10886 NM_001144756.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2099 rs4694450 4:72902750 C ENSESTG00000012061 ENSESTT00000030187 Transcript intron_variant - - - - - - rs4694450 4:72902750 C 10886 NM_053036.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2099 rs4694450 4:72902750 C CCDS3551.1 CCDS3551.1 Transcript intron_variant - - - - - - rs4694450 4:72902750 C ENSESTG00000012061 ENSESTT00000030208 Transcript upstream_gene_variant - - - - - - DISTANCE=2356 rs4694450 4:72902750 C ENSESTG00000012061 ENSESTT00000030191 Transcript intron_variant - - - - - - rs4607186 4:72931110 T CCDS47072.1 CCDS47072.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3629 rs4607186 4:72931110 T 10886 NM_053036.2 Transcript intron_variant - - - - - - rs4607186 4:72931110 T CCDS3551.1 CCDS3551.1 Transcript intron_variant - - - - - - rs4607186 4:72931110 T ENSESTG00000012061 ENSESTT00000030208 Transcript intron_variant - - - - - - rs4607186 4:72931110 T ENSESTG00000012061 ENSESTT00000030191 Transcript intron_variant - - - - - - rs4607186 4:72931110 T 10886 NM_001144756.1 Transcript intron_variant - - - - - - rs4607186 4:72931110 T 10886 NM_004885.2 Transcript intron_variant - - - - - - rs4607186 4:72931110 T ENSESTG00000012061 ENSESTT00000030187 Transcript intron_variant - - - - - - rs11939151 4:73057273 G - - - intergenic_variant - - - - - - rs12643019 4:73082203 T - - - intergenic_variant - - - - - - rs1085945 4:73357553 A ENSESTG00000012078 ENSESTT00000030224 Transcript intron_variant - - - - - - rs1085945 4:73357553 A 9508 NM_014243.2 Transcript intron_variant - - - - - - rs1085945 4:73357553 A ENSESTG00000012078 ENSESTT00000030227 Transcript intron_variant - - - - - - rs1085945 4:73357553 A CCDS3553.1 CCDS3553.1 Transcript intron_variant - - - - - - rs788938 4:73380355 T ENSESTG00000012078 ENSESTT00000030224 Transcript intron_variant - - - - - - rs788938 4:73380355 T 9508 NM_014243.2 Transcript intron_variant - - - - - - rs788938 4:73380355 T ENSESTG00000012078 ENSESTT00000030227 Transcript intron_variant - - - - - - rs788938 4:73380355 T CCDS3553.1 CCDS3553.1 Transcript intron_variant - - - - - - rs6446843 4:73442497 C - - - intergenic_variant - - - - - - rs4694500 4:73456482 T - - - intergenic_variant - - - - - - rs2170425 4:73493272 A - - - intergenic_variant - - - - - - rs1156393 4:73507719 T - - - intergenic_variant - - - - - - rs1600696 4:73538095 T - - - intergenic_variant - - - - - - rs2614331 4:73672128 A - - - intergenic_variant - - - - - - rs9291181 4:73854823 C - - - intergenic_variant - - - - - - rs6817301 4:73970302 A - ENSR00001242698 RegulatoryFeature regulatory_region_variant - - - - - - rs6817301 4:73970302 A CCDS34003.1 CCDS34003.1 Transcript intron_variant - - - - - - rs6817301 4:73970302 A ENSESTG00000032719 ENSESTT00000082782 Transcript intron_variant - - - - - - rs6817301 4:73970302 A 26057 NM_198889.1 Transcript intron_variant - - - - - - rs6817301 4:73970302 A ENSESTG00000032719 ENSESTT00000082748 Transcript intron_variant - - - - - - rs6817301 4:73970302 A CCDS34004.1 CCDS34004.1 Transcript intron_variant - - - - - - rs6817301 4:73970302 A 26057 NM_032217.3 Transcript intron_variant - - - - - - rs2137445 4:74046221 T CCDS34003.1 CCDS34003.1 Transcript intron_variant - - - - - - rs2137445 4:74046221 T ENSESTG00000032674 ENSESTT00000082553 Transcript intron_variant - - - - - - rs2137445 4:74046221 T 26057 NM_198889.1 Transcript intron_variant - - - - - - rs2137445 4:74046221 T CCDS34004.1 CCDS34004.1 Transcript intron_variant - - - - - - rs2137445 4:74046221 T 26057 NM_032217.3 Transcript intron_variant - - - - - - rs7688302 4:74085036 T CCDS34003.1 CCDS34003.1 Transcript intron_variant - - - - - - rs7688302 4:74085036 T ENSESTG00000032674 ENSESTT00000082553 Transcript intron_variant - - - - - - rs7688302 4:74085036 T 26057 NM_198889.1 Transcript intron_variant - - - - - - rs7688302 4:74085036 T CCDS34004.1 CCDS34004.1 Transcript intron_variant - - - - - - rs7688302 4:74085036 T 26057 NM_032217.3 Transcript intron_variant - - - - - - rs1881610 4:74394642 G ENSESTG00000032646 ENSESTT00000082404 Transcript intron_variant - - - - - - rs1881610 4:74394642 G 728040 NR_046377.1 Transcript downstream_gene_variant - - - - - - DISTANCE=392 rs1881610 4:74394642 G ENSESTG00000032646 ENSESTT00000082410 Transcript downstream_gene_variant - - - - - - DISTANCE=203 rs1247640 4:74457471 C ENSESTG00000032654 ENSESTT00000082447 Transcript intron_variant - - - - - - rs1247640 4:74457471 C 166824 NM_201431.2 Transcript intron_variant - - - - - - rs1247640 4:74457471 C 166824 NM_001270392.1 Transcript intron_variant - - - - - - rs1247640 4:74457471 C 166824 NM_177532.4 Transcript intron_variant - - - - - - rs1247640 4:74457471 C CCDS58905.1 CCDS58905.1 Transcript intron_variant - - - - - - rs1247640 4:74457471 C CCDS3559.1 CCDS3559.1 Transcript intron_variant - - - - - - rs1247640 4:74457471 C ENSESTG00000032654 ENSESTT00000082476 Transcript intron_variant - - - - - - rs1247640 4:74457471 C 166824 NM_001270391.1 Transcript intron_variant - - - - - - rs1247640 4:74457471 C CCDS58904.1 CCDS58904.1 Transcript intron_variant - - - - - - rs1247640 4:74457471 C CCDS3558.1 CCDS3558.1 Transcript intron_variant - - - - - - rs1528914 4:74474885 C - ENSR00001432010 RegulatoryFeature regulatory_region_variant - - - - - - rs1528914 4:74474885 C ENSESTG00000032654 ENSESTT00000082447 Transcript intron_variant - - - - - - rs1528914 4:74474885 C 166824 NM_201431.2 Transcript intron_variant - - - - - - rs1528914 4:74474885 C 166824 NM_001270392.1 Transcript intron_variant - - - - - - rs1528914 4:74474885 C ENSESTG00000032654 ENSESTT00000082458 Transcript intron_variant - - - - - - rs1528914 4:74474885 C 166824 NM_177532.4 Transcript intron_variant - - - - - - rs1528914 4:74474885 C CCDS58905.1 CCDS58905.1 Transcript intron_variant - - - - - - rs1528914 4:74474885 C CCDS3559.1 CCDS3559.1 Transcript intron_variant - - - - - - rs1528914 4:74474885 C ENSESTG00000032654 ENSESTT00000082476 Transcript intron_variant - - - - - - rs1528914 4:74474885 C 166824 NM_001270391.1 Transcript intron_variant - - - - - - rs1528914 4:74474885 C CCDS58904.1 CCDS58904.1 Transcript intron_variant - - - - - - rs1528914 4:74474885 C CCDS3558.1 CCDS3558.1 Transcript intron_variant - - - - - - rs1247594 4:74485645 G ENSESTG00000032654 ENSESTT00000082447 Transcript intron_variant - - - - - - rs1247594 4:74485645 G 166824 NM_201431.2 Transcript intron_variant - - - - - - rs1247594 4:74485645 G 166824 NM_001270392.1 Transcript intron_variant - - - - - - rs1247594 4:74485645 G 166824 NM_177532.4 Transcript intron_variant - - - - - - rs1247594 4:74485645 G ENSESTG00000032654 ENSESTT00000082458 Transcript intron_variant - - - - - - rs1247594 4:74485645 G CCDS58905.1 CCDS58905.1 Transcript intron_variant - - - - - - rs1247594 4:74485645 G ENSESTG00000032654 ENSESTT00000082476 Transcript intron_variant - - - - - - rs1247594 4:74485645 G 166824 NM_001270391.1 Transcript intron_variant - - - - - - rs1247594 4:74485645 G CCDS3558.1 CCDS3558.1 Transcript intron_variant - - - - - - rs1247573 4:74520670 T - - - intergenic_variant - - - - - - rs1247623 4:74564257 C - ENSR00001242804 RegulatoryFeature regulatory_region_variant - - - - - - rs1247623 4:74564257 C - - - intergenic_variant - - - - - - rs2145616 4:74632528 C - - - intergenic_variant - - - - - - rs3111699 4:74717724 G CCDS3561.1 CCDS3561.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1356 rs3111699 4:74717724 G 5197 NM_002620.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1289 rs3111699 4:74717724 G ENSESTG00000011685 ENSESTT00000029296 Transcript downstream_gene_variant - - - - - - DISTANCE=2943 rs352001 4:74844782 G - ENSR00001432059 RegulatoryFeature regulatory_region_variant - - - - - - rs352001 4:74844782 G 5196 NM_002619.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1760 rs352001 4:74844782 G CCDS3562.1 CCDS3562.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2139 rs497427 4:74860838 C 6374 NM_002994.3 Transcript downstream_gene_variant - - - - - - DISTANCE=521 rs497427 4:74860838 C ENSESTG00000011832 ENSESTT00000029669 Transcript downstream_gene_variant - - - - - - DISTANCE=2222 rs497427 4:74860838 C CCDS34006.1 CCDS34006.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2516 rs4311284 4:74976810 G - - - intergenic_variant - - - - - - rs506678 4:75014690 A ENSESTG00000011702 ENSESTT00000029343 Transcript intron_variant - - - - - - rs539662 4:75039707 T 441024 NM_001144978.1 Transcript intron_variant - - - - - - rs539662 4:75039707 T CCDS47075.1 CCDS47075.1 Transcript intron_variant - - - - - - rs539662 4:75039707 T ENSESTG00000011702 ENSESTT00000029343 Transcript intron_variant - - - - - - rs479496 4:75041363 A 441024 NM_001144978.1 Transcript intron_variant - - - - - - rs479496 4:75041363 A CCDS47075.1 CCDS47075.1 Transcript intron_variant - - - - - - rs479496 4:75041363 A ENSESTG00000011702 ENSESTT00000029343 Transcript intron_variant - - - - - - rs497461 4:75044588 G 441024 NM_001144978.1 Transcript intron_variant - - - - - - rs497461 4:75044588 G CCDS47075.1 CCDS47075.1 Transcript intron_variant - - - - - - rs497461 4:75044588 G ENSESTG00000011702 ENSESTT00000029343 Transcript intron_variant - - - - - - rs561844 4:75046465 G 441024 NM_001144978.1 Transcript intron_variant - - - - - - rs561844 4:75046465 G CCDS47075.1 CCDS47075.1 Transcript intron_variant - - - - - - rs561844 4:75046465 G ENSESTG00000011702 ENSESTT00000029343 Transcript 3_prime_UTR_variant 603 - - - - - rs4561988 4:75783724 G - - - intergenic_variant - - - - - - rs6533255 4:75824449 T - - - intergenic_variant - - - - - - rs4859852 4:75826838 C - - - intergenic_variant - - - - - - rs1863423 4:75977712 C 25849 NM_015393.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2387 rs6856486 4:76074396 C - - - intergenic_variant - - - - - - rs965729 4:76135988 C - - - intergenic_variant - - - - - - rs12186269 4:76158009 T - - - intergenic_variant - - - - - - rs1874586 4:76172090 C - - - intergenic_variant - - - - - - rs2132805 4:76174822 C - - - intergenic_variant - - - - - - rs6836862 4:76245558 A - - - intergenic_variant - - - - - - rs6531774 4:76513890 C CCDS3570.1 CCDS3570.1 Transcript intron_variant - - - - - - rs6531774 4:76513890 C 8999 NM_003948.3 Transcript intron_variant - - - - - - rs324684 4:76727069 C ENSESTG00000016114 ENSESTT00000040648 Transcript intron_variant - - - - - - rs324684 4:76727069 C ENSESTG00000016114 ENSESTT00000040595 Transcript intron_variant - - - - - - rs324684 4:76727069 C ENSESTG00000016114 ENSESTT00000040641 Transcript intron_variant - - - - - - rs324684 4:76727069 C ENSESTG00000016114 ENSESTT00000040626 Transcript intron_variant - - - - - - rs324684 4:76727069 C 8615 NM_003715.2 Transcript intron_variant - - - - - - rs324699 4:76735187 T ENSESTG00000016114 ENSESTT00000040648 Transcript downstream_gene_variant - - - - - - DISTANCE=78 rs324699 4:76735187 T ENSESTG00000016114 ENSESTT00000040595 Transcript downstream_gene_variant - - - - - - DISTANCE=78 rs324699 4:76735187 T ENSESTG00000016114 ENSESTT00000040641 Transcript downstream_gene_variant - - - - - - DISTANCE=78 rs324699 4:76735187 T ENSESTG00000016114 ENSESTT00000040626 Transcript downstream_gene_variant - - - - - - DISTANCE=78 rs324699 4:76735187 T 8615 NM_003715.2 Transcript 3_prime_UTR_variant 3680 - - - - - rs6531950 4:76760898 G - - - intergenic_variant - - - - - - rs4356931 4:76762399 T - - - intergenic_variant - - - - - - rs924936 4:76769420 T - ENSR00001243203 RegulatoryFeature regulatory_region_variant - - - - - - rs924936 4:76769420 T - - - intergenic_variant - - - - - - rs2056021 4:76797179 G 5470 NM_006239.2 Transcript intron_variant - - - - - - rs2056021 4:76797179 G CCDS34013.1 CCDS34013.1 Transcript intron_variant - - - - - - rs1441915 4:77197015 G - ENSR00001432237 RegulatoryFeature regulatory_region_variant - - - - - - rs1441915 4:77197015 G 100631383 NM_001242939.1 Transcript intron_variant - - - - - - rs1441915 4:77197015 G ENSESTG00000016344 ENSESTT00000041035 Transcript downstream_gene_variant - - - - - - DISTANCE=3930 rs1441915 4:77197015 G ENSESTG00000016344 ENSESTT00000040991 Transcript intron_variant - - - - - - rs1441915 4:77197015 G 100129583 NM_001242936.1 Transcript intron_variant - - - - - - rs1441915 4:77197015 G 100129583 NM_001136570.2 Transcript intron_variant - - - - - - rs1441915 4:77197015 G CCDS47081.1 CCDS47081.1 Transcript intron_variant - - - - - - rs1441915 4:77197015 G CCDS58908.1 CCDS58908.1 Transcript intron_variant - - - - - - rs1441915 4:77197015 G ENSESTG00000016344 ENSESTT00000041031 Transcript intron_variant - - - - - - rs1441915 4:77197015 G CCDS58907.1 CCDS58907.1 Transcript intron_variant - - - - - - rs6532477 4:77474996 T 57619 NM_020859.3 Transcript intron_variant - - - - - - rs6532477 4:77474996 T ENSESTG00000016082 ENSESTT00000040323 Transcript intron_variant - - - - - - rs6532477 4:77474996 T CCDS3579.2 CCDS3579.2 Transcript intron_variant - - - - - - rs6532477 4:77474996 T ENSESTG00000016082 ENSESTT00000040318 Transcript intron_variant - - - - - - rs6532477 4:77474996 T ENSESTG00000016082 ENSESTT00000040339 Transcript upstream_gene_variant - - - - - - DISTANCE=1771 rs6532494 4:77512174 G - ENSR00001243317 RegulatoryFeature regulatory_region_variant - - - - - - rs6532494 4:77512174 G 57619 NM_020859.3 Transcript intron_variant - - - - - - rs6532494 4:77512174 G ENSESTG00000016082 ENSESTT00000040345 Transcript intron_variant - - - - - - rs6532494 4:77512174 G ENSESTG00000016082 ENSESTT00000040323 Transcript intron_variant - - - - - - rs6532494 4:77512174 G CCDS3579.2 CCDS3579.2 Transcript intron_variant - - - - - - rs6532494 4:77512174 G ENSESTG00000016082 ENSESTT00000040357 Transcript intron_variant - - - - - - rs6532494 4:77512174 G ENSESTG00000016082 ENSESTT00000040367 Transcript intron_variant - - - - - - rs6532494 4:77512174 G ENSESTG00000016082 ENSESTT00000040339 Transcript intron_variant - - - - - - rs13125279 4:77758051 A - ENSR00001432310 RegulatoryFeature regulatory_region_variant - - - - - - rs13125279 4:77758051 A - - - intergenic_variant - - - - - - rs4328940 4:77892144 A ENSESTG00000032926 ENSESTT00000083309 Transcript intron_variant - - - - - - rs4328940 4:77892144 A ENSESTG00000032926 ENSESTT00000083290 Transcript intron_variant - - - - - - rs4328940 4:77892144 A 55752 NM_018243.2 Transcript intron_variant - - - - - - rs4328940 4:77892144 A CCDS34018.1 CCDS34018.1 Transcript intron_variant - - - - - - rs4328940 4:77892144 A ENSESTG00000032926 ENSESTT00000083307 Transcript intron_variant - - - - - - rs4328940 4:77892144 A ENSESTG00000032926 ENSESTT00000083285 Transcript intron_variant - - - - - - rs4328940 4:77892144 A ENSESTG00000032926 ENSESTT00000083301 Transcript intron_variant - - - - - - rs10776493 4:78396048 T - - - intergenic_variant - - - - - - rs1867105 4:78416070 G - - - intergenic_variant - - - - - - rs4859507 4:78756377 A - - - intergenic_variant - - - - - - rs7683292 4:79092900 G - ENSR00001432432 RegulatoryFeature regulatory_region_variant - - - - - - rs7683292 4:79092900 G 80144 NM_025074.6 Transcript intron_variant - - - - - - rs7683292 4:79092900 G ENSESTG00000034873 ENSESTT00000088150 Transcript intron_variant - - - - - - rs7683292 4:79092900 G CCDS54771.1 CCDS54771.1 Transcript intron_variant - - - - - - rs7683292 4:79092900 G CCDS54772.1 CCDS54772.1 Transcript intron_variant - - - - - - rs7683292 4:79092900 G ENSESTG00000034873 ENSESTT00000088154 Transcript intron_variant - - - - - - rs7683292 4:79092900 G 80144 NM_001166133.1 Transcript intron_variant - - - - - - rs2866999 4:79108485 C 80144 NM_025074.6 Transcript intron_variant - - - - - - rs2866999 4:79108485 C ENSESTG00000034873 ENSESTT00000088150 Transcript intron_variant - - - - - - rs2866999 4:79108485 C CCDS54771.1 CCDS54771.1 Transcript intron_variant - - - - - - rs2866999 4:79108485 C CCDS54772.1 CCDS54772.1 Transcript intron_variant - - - - - - rs2866999 4:79108485 C ENSESTG00000034873 ENSESTT00000088154 Transcript intron_variant - - - - - - rs2866999 4:79108485 C 80144 NM_001166133.1 Transcript intron_variant - - - - - - rs11098104 4:79164699 C 80144 NM_025074.6 Transcript intron_variant - - - - - - rs11098104 4:79164699 C ENSESTG00000034873 ENSESTT00000088150 Transcript intron_variant - - - - - - rs11098104 4:79164699 C CCDS54771.1 CCDS54771.1 Transcript intron_variant - - - - - - rs11098104 4:79164699 C CCDS54772.1 CCDS54772.1 Transcript intron_variant - - - - - - rs11098104 4:79164699 C ENSESTG00000034873 ENSESTT00000088154 Transcript intron_variant - - - - - - rs11098104 4:79164699 C 80144 NM_001166133.1 Transcript intron_variant - - - - - - rs4975149 4:79691085 G - ENSR00001243757 RegulatoryFeature regulatory_region_variant - - - - - - rs4975149 4:79691085 G - - - intergenic_variant - - - - - - rs7689396 4:79784071 G ENSESTG00000012087 ENSESTT00000030245 Transcript upstream_gene_variant - - - - - - DISTANCE=3340 rs7689396 4:79784071 G ENSESTG00000012072 ENSESTT00000030238 Transcript intron_variant - - - - - - rs7689396 4:79784071 G ENSESTG00000012072 ENSESTT00000030234 Transcript intron_variant - - - - - - rs7689396 4:79784071 G CCDS47083.1 CCDS47083.1 Transcript intron_variant - - - - - - rs7689396 4:79784071 G CCDS34019.1 CCDS34019.1 Transcript intron_variant - - - - - - rs7689396 4:79784071 G 55589 NM_017593.3 Transcript intron_variant - - - - - - rs7689396 4:79784071 G 55589 NM_198892.1 Transcript intron_variant - - - - - - rs7674019 4:80049783 T 100505875 NR_038342.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11943666 4:80751587 C 118425 NR_026555.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4337684 4:80953448 T 118429 NM_058172.5 Transcript intron_variant - - - - - - rs4337684 4:80953448 T CCDS47086.1 CCDS47086.1 Transcript intron_variant - - - - - - rs4337684 4:80953448 T 118429 NM_001145794.1 Transcript intron_variant - - - - - - rs4337684 4:80953448 T CCDS47085.1 CCDS47085.1 Transcript intron_variant - - - - - - rs4337684 4:80953448 T ENSESTG00000011965 ENSESTT00000030039 Transcript intron_variant - - - - - - rs4558868 4:81291909 T CCDS56336.1 CCDS56336.1 Transcript intron_variant - - - - - - rs4558868 4:81291909 T 255119 NM_152770.2 Transcript intron_variant - - - - - - rs4558868 4:81291909 T CCDS3587.1 CCDS3587.1 Transcript intron_variant - - - - - - rs4558868 4:81291909 T 255119 NM_001206997.1 Transcript intron_variant - - - - - - rs4495031 4:81470459 T CCDS56336.1 CCDS56336.1 Transcript intron_variant - - - - - - rs4495031 4:81470459 T 255119 NM_152770.2 Transcript intron_variant - - - - - - rs4495031 4:81470459 T CCDS3587.1 CCDS3587.1 Transcript intron_variant - - - - - - rs4495031 4:81470459 T 255119 NM_001206997.1 Transcript intron_variant - - - - - - rs6535180 4:81741410 C CCDS56336.1 CCDS56336.1 Transcript intron_variant - - - - - - rs6535180 4:81741410 C 255119 NM_152770.2 Transcript intron_variant - - - - - - rs6535180 4:81741410 C CCDS3587.1 CCDS3587.1 Transcript intron_variant - - - - - - rs6535180 4:81741410 C 255119 NM_001206997.1 Transcript intron_variant - - - - - - rs6854975 4:81945335 T - - - intergenic_variant - - - - - - rs9307777 4:81955781 T CCDS3588.1 CCDS3588.1 Transcript intron_variant - - - - - - rs9307777 4:81955781 T 651 NM_001201.2 Transcript intron_variant - - - - - - rs1495635 4:81963493 T CCDS3588.1 CCDS3588.1 Transcript intron_variant - - - - - - rs1495635 4:81963493 T ENSESTG00000002008 ENSESTT00000004998 Transcript upstream_gene_variant - - - - - - DISTANCE=3448 rs1495635 4:81963493 T 651 NM_001201.2 Transcript intron_variant - - - - - - rs6822169 4:81963645 G CCDS3588.1 CCDS3588.1 Transcript intron_variant - - - - - - rs6822169 4:81963645 G ENSESTG00000002008 ENSESTT00000004998 Transcript upstream_gene_variant - - - - - - DISTANCE=3296 rs6822169 4:81963645 G 651 NM_001201.2 Transcript intron_variant - - - - - - rs5004402 4:81975529 A CCDS3588.1 CCDS3588.1 Transcript downstream_gene_variant - - - - - - DISTANCE=839 rs5004402 4:81975529 A ENSESTG00000002008 ENSESTT00000004998 Transcript downstream_gene_variant - - - - - - DISTANCE=191 rs5004402 4:81975529 A 651 NM_001201.2 Transcript 3_prime_UTR_variant 2578 - - - - - rs10019455 4:81977730 T CCDS3588.1 CCDS3588.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3040 rs10019455 4:81977730 T ENSESTG00000002008 ENSESTT00000004998 Transcript downstream_gene_variant - - - - - - DISTANCE=2392 rs10019455 4:81977730 T 651 NM_001201.2 Transcript 3_prime_UTR_variant 4779 - - - - - rs1963598 4:81989229 C - - - intergenic_variant - - - - - - rs6841457 4:82029717 G CCDS3589.1 CCDS3589.1 Transcript intron_variant - - - - - - rs6841457 4:82029717 G ENSESTG00000002050 ENSESTT00000005074 Transcript intron_variant - - - - - - rs6841457 4:82029717 G ENSESTG00000002050 ENSESTT00000005082 Transcript upstream_gene_variant - - - - - - DISTANCE=2671 rs6841457 4:82029717 G 5593 NM_006259.1 Transcript intron_variant - - - - - - rs1899943 4:82470580 A - - - intergenic_variant - - - - - - rs1463798 4:82673366 C ENSESTG00000002015 ENSESTT00000005005 Transcript intron_variant - - - - - - rs1463798 4:82673366 C ENSESTG00000002015 ENSESTT00000005003 Transcript intron_variant - - - - - - rs4568235 4:83595527 A ENSESTG00000000552 ENSESTT00000001347 Transcript intron_variant - - - - - - rs4568235 4:83595527 A 79966 NM_024906.2 Transcript intron_variant - - - - - - rs4568235 4:83595527 A 79966 NM_001037582.2 Transcript intron_variant - - - - - - rs4568235 4:83595527 A CCDS3595.1 CCDS3595.1 Transcript intron_variant - - - - - - rs4568235 4:83595527 A ENSESTG00000000552 ENSESTT00000001339 Transcript intron_variant - - - - - - rs4568235 4:83595527 A CCDS34024.1 CCDS34024.1 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019442 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019454 Transcript intron_variant - - - - - - rs4632651 4:83753554 A CCDS47088.1 CCDS47088.1 Transcript intron_variant - - - - - - rs4632651 4:83753554 A 22872 NM_016211.3 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019436 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019479 Transcript intron_variant - - - - - - rs4632651 4:83753554 A 22872 NM_001077206.2 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019486 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019425 Transcript intron_variant - - - - - - rs4632651 4:83753554 A 22872 NM_001191049.1 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019452 Transcript intron_variant - - - - - - rs4632651 4:83753554 A 22872 NM_001077208.2 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019466 Transcript intron_variant - - - - - - rs4632651 4:83753554 A CCDS43244.1 CCDS43244.1 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019420 Transcript intron_variant - - - - - - rs4632651 4:83753554 A CCDS54773.1 CCDS54773.1 Transcript intron_variant - - - - - - rs4632651 4:83753554 A CCDS3597.1 CCDS3597.1 Transcript intron_variant - - - - - - rs4632651 4:83753554 A 22872 NM_014933.3 Transcript intron_variant - - - - - - rs4632651 4:83753554 A CCDS3596.1 CCDS3596.1 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019487 Transcript intron_variant - - - - - - rs4632651 4:83753554 A 22872 NM_001077207.2 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019422 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019482 Transcript intron_variant - - - - - - rs4632651 4:83753554 A ENSESTG00000007673 ENSESTT00000019423 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019442 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019490 Transcript downstream_gene_variant - - - - - - DISTANCE=4114 rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019454 Transcript intron_variant - - - - - - rs6839005 4:83762264 T CCDS47088.1 CCDS47088.1 Transcript intron_variant - - - - - - rs6839005 4:83762264 T 22872 NM_016211.3 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019436 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019479 Transcript intron_variant - - - - - - rs6839005 4:83762264 T 22872 NM_001077206.2 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019486 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019425 Transcript intron_variant - - - - - - rs6839005 4:83762264 T 22872 NM_001191049.1 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019452 Transcript intron_variant - - - - - - rs6839005 4:83762264 T 22872 NM_001077208.2 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019466 Transcript intron_variant - - - - - - rs6839005 4:83762264 T CCDS43244.1 CCDS43244.1 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019420 Transcript intron_variant - - - - - - rs6839005 4:83762264 T CCDS54773.1 CCDS54773.1 Transcript intron_variant - - - - - - rs6839005 4:83762264 T CCDS3597.1 CCDS3597.1 Transcript intron_variant - - - - - - rs6839005 4:83762264 T 22872 NM_014933.3 Transcript intron_variant - - - - - - rs6839005 4:83762264 T CCDS3596.1 CCDS3596.1 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019487 Transcript intron_variant - - - - - - rs6839005 4:83762264 T 22872 NM_001077207.2 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019422 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019482 Transcript intron_variant - - - - - - rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019473 Transcript downstream_gene_variant - - - - - - DISTANCE=4114 rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019469 Transcript downstream_gene_variant - - - - - - DISTANCE=4114 rs6839005 4:83762264 T ENSESTG00000007673 ENSESTT00000019423 Transcript intron_variant - - - - - - rs11736035 4:84005474 C - ENSR00001244308 RegulatoryFeature regulatory_region_variant - - - - - - rs11736035 4:84005474 C - - - intergenic_variant - - - - - - rs2047209 4:84344235 T CCDS3603.1 CCDS3603.1 Transcript intron_variant - - - - - - rs2047209 4:84344235 T ENSESTG00000007491 ENSESTT00000018926 Transcript upstream_gene_variant - - - - - - DISTANCE=1354 rs2047209 4:84344235 T 113510 NM_133636.2 Transcript intron_variant - - - - - - rs2047209 4:84344235 T ENSESTG00000007491 ENSESTT00000018930 Transcript upstream_gene_variant - - - - - - DISTANCE=4874 rs2047209 4:84344235 T ENSESTG00000007491 ENSESTT00000018890 Transcript intron_variant - - - - - - rs2199080 4:84627677 A - - - intergenic_variant - - - - - - rs2129967 4:84701410 G - - - intergenic_variant - - - - - - rs1910953 4:84917070 G ENSESTG00000013689 ENSESTT00000034214 Transcript intron_variant - - - - - - rs348711 4:85197776 T ENSESTG00000013680 ENSESTT00000034202 Transcript intron_variant - - - - - - rs348707 4:85238135 T - - - intergenic_variant - - - - - - rs6856016 4:85568216 G ENSESTG00000013660 ENSESTT00000034165 Transcript downstream_gene_variant - - - - - - DISTANCE=2484 rs6856016 4:85568216 G 1040 NM_001263.3 Transcript intron_variant - - - - - - rs6856016 4:85568216 G CCDS3608.1 CCDS3608.1 Transcript intron_variant - - - - - - rs6856016 4:85568216 G ENSESTG00000013598 ENSESTT00000034058 Transcript intron_variant - - - - - - rs4568231 4:85854816 A ENSESTG00000030408 ENSESTT00000076592 Transcript intron_variant - - - - - - rs4568231 4:85854816 A ENSESTG00000030408 ENSESTT00000076609 Transcript intron_variant - - - - - - rs4568231 4:85854816 A ENSESTG00000030408 ENSESTT00000076582 Transcript intron_variant - - - - - - rs4568231 4:85854816 A ENSESTG00000030408 ENSESTT00000076512 Transcript intron_variant - - - - - - rs4568231 4:85854816 A ENSESTG00000030408 ENSESTT00000076521 Transcript intron_variant - - - - - - rs4568231 4:85854816 A 23001 NM_014991.4 Transcript intron_variant - - - - - - rs11930265 4:85961764 T - - - intergenic_variant - - - - - - rs7699433 4:85972734 C - ENSR00001432768 RegulatoryFeature regulatory_region_variant - - - - - - rs7699433 4:85972734 C - - - intergenic_variant - - - - - - rs4279198 4:86088092 G - - - intergenic_variant - - - - - - rs1351550 4:86516978 A 83478 NM_001025616.2 Transcript intron_variant - - - - - - rs1351550 4:86516978 A CCDS34025.1 CCDS34025.1 Transcript intron_variant - - - - - - rs4485813 4:86611408 G 83478 NM_001025616.2 Transcript intron_variant - - - - - - rs4485813 4:86611408 G CCDS34025.1 CCDS34025.1 Transcript intron_variant - - - - - - rs921563 4:86703525 A ENSESTG00000032220 ENSESTT00000081358 Transcript intron_variant - - - - - - rs921563 4:86703525 A 83478 NM_001025616.2 Transcript intron_variant - - - - - - rs921563 4:86703525 A 83478 NM_001042669.1 Transcript intron_variant - - - - - - rs921563 4:86703525 A CCDS34025.1 CCDS34025.1 Transcript intron_variant - - - - - - rs9998829 4:87303418 T ENSESTG00000032285 ENSESTT00000081503 Transcript intron_variant - - - - - - rs9998829 4:87303418 T 5602 NM_002753.3 Transcript intron_variant - - - - - - rs9998829 4:87303418 T ENSESTG00000032285 ENSESTT00000081490 Transcript intron_variant - - - - - - rs7673015 4:87771338 T - ENSR00001244773 RegulatoryFeature regulatory_region_variant - - - - - - rs7673015 4:87771338 T 345274 NM_197965.2 Transcript upstream_gene_variant - - - - - - DISTANCE=922 rs7673015 4:87771338 T CCDS3614.1 CCDS3614.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1070 rs342464 4:88056925 G CCDS54775.1 CCDS54775.1 Transcript downstream_gene_variant - - - - - - DISTANCE=72 rs342464 4:88056925 G 4299 NM_005935.2 Transcript 3_prime_UTR_variant 4112 - - - - - rs342464 4:88056925 G ENSESTG00000029276 ENSESTT00000073797 Transcript downstream_gene_variant - - - - - - DISTANCE=1127 rs342464 4:88056925 G 4299 NM_001166693.1 Transcript 3_prime_UTR_variant 4004 - - - - - rs342464 4:88056925 G CCDS3616.1 CCDS3616.1 Transcript downstream_gene_variant - - - - - - DISTANCE=72 rs2627684 4:88660024 A - - - intergenic_variant - - - - - - rs6850822 4:89151034 C ENSESTG00000000801 ENSESTT00000001955 Transcript intron_variant - - - - - - rs6850822 4:89151034 C 9429 NM_001257386.1 Transcript intron_variant - - - - - - rs6820724 4:89256058 C ENSESTG00000000693 ENSESTT00000001661 Transcript intron_variant - - - - - - rs4298105 4:89350958 G CCDS54777.1 CCDS54777.1 Transcript intron_variant - - - - - - rs4298105 4:89350958 G 55008 NM_017912.3 Transcript intron_variant - - - - - - rs4298105 4:89350958 G ENSESTG00000000696 ENSESTT00000001743 Transcript intron_variant - - - - - - rs4298105 4:89350958 G ENSESTG00000000696 ENSESTT00000001735 Transcript intron_variant - - - - - - rs4298105 4:89350958 G ENSESTG00000000696 ENSESTT00000001739 Transcript intron_variant - - - - - - rs4298105 4:89350958 G 55008 NM_001165136.1 Transcript intron_variant - - - - - - rs4298105 4:89350958 G CCDS47098.1 CCDS47098.1 Transcript intron_variant - - - - - - rs6532180 4:90562215 C - ENSR00001245284 RegulatoryFeature regulatory_region_variant - - - - - - rs6532180 4:90562215 C - - - intergenic_variant - - - - - - rs990638 4:90925106 G - - - intergenic_variant - - - - - - rs7692853 4:91120367 C ENSESTG00000023309 ENSESTT00000058854 Transcript intron_variant - - - - - - rs7692853 4:91120367 C 401145 NM_001145065.1 Transcript intron_variant - - - - - - rs4692951 4:91323681 A ENSESTG00000023309 ENSESTT00000058867 Transcript intron_variant - - - - - - rs4692951 4:91323681 A CCDS47099.1 CCDS47099.1 Transcript intron_variant - - - - - - rs4692951 4:91323681 A 401145 NM_207491.2 Transcript intron_variant - - - - - - rs4692951 4:91323681 A 401145 NM_001145065.1 Transcript intron_variant - - - - - - rs4692951 4:91323681 A CCDS47100.1 CCDS47100.1 Transcript intron_variant - - - - - - rs9684386 4:91560826 C ENSESTG00000023343 ENSESTT00000058905 Transcript intron_variant - - - - - - rs9684386 4:91560826 C CCDS47099.1 CCDS47099.1 Transcript intron_variant - - - - - - rs9684386 4:91560826 C 401145 NM_207491.2 Transcript intron_variant - - - - - - rs9684386 4:91560826 C 401145 NM_001145065.1 Transcript intron_variant - - - - - - rs9684386 4:91560826 C CCDS47100.1 CCDS47100.1 Transcript intron_variant - - - - - - rs6832125 4:91561985 C ENSESTG00000023343 ENSESTT00000058905 Transcript intron_variant - - - - - - rs6832125 4:91561985 C CCDS47099.1 CCDS47099.1 Transcript intron_variant - - - - - - rs6832125 4:91561985 C 401145 NM_207491.2 Transcript intron_variant - - - - - - rs6832125 4:91561985 C 401145 NM_001145065.1 Transcript intron_variant - - - - - - rs6832125 4:91561985 C CCDS47100.1 CCDS47100.1 Transcript intron_variant - - - - - - rs1288753 4:91871744 G - ENSR00001245409 RegulatoryFeature regulatory_region_variant - - - - - - rs1288753 4:91871744 G ENSESTG00000028157 ENSESTT00000070795 Transcript intron_variant - - - - - - rs1288753 4:91871744 G ENSESTG00000028179 ENSESTT00000070846 Transcript intron_variant - - - - - - rs1288753 4:91871744 G CCDS47099.1 CCDS47099.1 Transcript intron_variant - - - - - - rs1288753 4:91871744 G 401145 NM_001145065.1 Transcript intron_variant - - - - - - rs2189187 4:92012480 G CCDS47099.1 CCDS47099.1 Transcript intron_variant - - - - - - rs2189187 4:92012480 G 401145 NM_001145065.1 Transcript intron_variant - - - - - - rs1015295 4:92039656 G CCDS47099.1 CCDS47099.1 Transcript intron_variant - - - - - - rs1015295 4:92039656 G 401145 NM_001145065.1 Transcript intron_variant - - - - - - rs1385869 4:92722479 C - - - intergenic_variant - - - - - - rs2199292 4:93079931 G ENSESTG00000022358 ENSESTT00000056417 Transcript intron_variant - - - - - - rs4693300 4:93555443 T 2895 NM_001510.2 Transcript intron_variant - - - - - - rs4693300 4:93555443 T CCDS3637.1 CCDS3637.1 Transcript intron_variant - - - - - - rs905486 4:94192939 C 2895 NM_001510.2 Transcript intron_variant - - - - - - rs905486 4:94192939 C ENSESTG00000004801 ENSESTT00000012188 Transcript intron_variant - - - - - - rs905486 4:94192939 C CCDS3637.1 CCDS3637.1 Transcript intron_variant - - - - - - rs1439544 4:94591532 T 2895 NM_001510.2 Transcript intron_variant - - - - - - rs1439544 4:94591532 T CCDS3637.1 CCDS3637.1 Transcript intron_variant - - - - - - rs6836843 4:94692734 T 2895 NM_001510.2 Transcript intron_variant - - - - - - rs6836843 4:94692734 T CCDS3637.1 CCDS3637.1 Transcript intron_variant - - - - - - rs2578153 4:94837323 C - - - intergenic_variant - - - - - - rs2621441 4:96218321 T 8633 NM_003728.3 Transcript intron_variant - - - - - - rs2621441 4:96218321 T ENSESTG00000004530 ENSESTT00000011473 Transcript intron_variant - - - - - - rs2621441 4:96218321 T CCDS3643.1 CCDS3643.1 Transcript intron_variant - - - - - - rs6419136 4:96449800 T 8633 NM_003728.3 Transcript intron_variant - - - - - - rs6419136 4:96449800 T CCDS3643.1 CCDS3643.1 Transcript intron_variant - - - - - - rs6419136 4:96449800 T ENSESTG00000004530 ENSESTT00000011445 Transcript intron_variant - - - - - - rs4699436 4:96515302 T - - - intergenic_variant - - - - - - rs1161113 4:96690059 C - - - intergenic_variant - - - - - - rs1583545 4:96787562 T - - - intergenic_variant - - - - - - rs7669210 4:96862967 T - - - intergenic_variant - - - - - - rs262456 4:97006516 C - - - intergenic_variant - - - - - - rs6854389 4:97403855 C - - - intergenic_variant - - - - - - rs1922855 4:97649739 C - - - intergenic_variant - - - - - - rs1876581 4:98436204 G ENSESTG00000000626 ENSESTT00000001493 Transcript intron_variant - - - - - - rs165245 4:98688174 G 285555 NM_174952.2 Transcript intron_variant - - - - - - rs165245 4:98688174 G CCDS3645.1 CCDS3645.1 Transcript intron_variant - - - - - - rs260888 4:98743495 C 285555 NM_174952.2 Transcript intron_variant - - - - - - rs260888 4:98743495 C CCDS3645.1 CCDS3645.1 Transcript intron_variant - - - - - - rs4699735 4:100140306 T - ENSR00001246085 RegulatoryFeature regulatory_region_variant - - - - - - rs4699735 4:100140306 T 130 NM_000672.3 Transcript missense_variant 98 4 2 C/S Tgt/Agt - PolyPhen=benign;SIFT=tolerated rs4699735 4:100140306 T 100507053 NR_037884.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4699735 4:100140306 T CCDS3647.1 CCDS3647.1 Transcript missense_variant 4 4 2 C/S Tgt/Agt - PolyPhen=benign;SIFT=tolerated rs4699735 4:100140306 T 130 NM_001102470.1 Transcript missense_variant 98 4 2 C/S Tgt/Agt - PolyPhen=benign;SIFT=tolerated rs4699735 4:100140306 T ENSESTG00000024254 ENSESTT00000061386 Transcript missense_variant 98 4 2 C/S Tgt/Agt - rs4699735 4:100140306 T ENSESTG00000024254 ENSESTT00000061413 Transcript 5_prime_UTR_variant 26 - - - - - rs4699735 4:100140306 T CCDS43255.1 CCDS43255.1 Transcript missense_variant 4 4 2 C/S Tgt/Agt - PolyPhen=benign;SIFT=tolerated rs2866150 4:100190782 C 100507053 NR_037884.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3114044 4:100191832 C 100507053 NR_037884.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6532853 4:101133964 G ENSESTG00000005955 ENSESTT00000015084 Transcript intron_variant - - - - - - rs1433262 4:101295204 A - - - intergenic_variant - - - - - - rs2866244 4:101718892 G - - - intergenic_variant - - - - - - rs2866254 4:101834755 A - - - intergenic_variant - - - - - - rs2850970 4:102184007 A ENSESTG00000018990 ENSESTT00000048018 Transcript intron_variant - - - - - - rs2850970 4:102184007 A 5530 NM_001130692.1 Transcript intron_variant - - - - - - rs2850970 4:102184007 A CCDS47113.1 CCDS47113.1 Transcript intron_variant - - - - - - rs2850970 4:102184007 A CCDS34037.1 CCDS34037.1 Transcript intron_variant - - - - - - rs2850970 4:102184007 A ENSESTG00000018990 ENSESTT00000047951 Transcript intron_variant - - - - - - rs2850970 4:102184007 A ENSESTG00000018990 ENSESTT00000047953 Transcript intron_variant - - - - - - rs2850970 4:102184007 A ENSESTG00000018990 ENSESTT00000047993 Transcript intron_variant - - - - - - rs2850970 4:102184007 A ENSESTG00000018990 ENSESTT00000047988 Transcript intron_variant - - - - - - rs2850970 4:102184007 A 5530 NM_001130691.1 Transcript intron_variant - - - - - - rs2850970 4:102184007 A ENSESTG00000018990 ENSESTT00000047985 Transcript intron_variant - - - - - - rs2850970 4:102184007 A 5530 NM_000944.4 Transcript intron_variant - - - - - - rs2850970 4:102184007 A ENSESTG00000018990 ENSESTT00000047808 Transcript intron_variant - - - - - - rs2850970 4:102184007 A CCDS47114.1 CCDS47114.1 Transcript intron_variant - - - - - - rs2850970 4:102184007 A ENSESTG00000018990 ENSESTT00000047815 Transcript intron_variant - - - - - - rs2866432 4:102639541 C - - - intergenic_variant - - - - - - rs3113674 4:102957235 T CCDS47115.1 CCDS47115.1 Transcript intron_variant - - - - - - rs3113674 4:102957235 T 55024 NM_001127507.2 Transcript intron_variant - - - - - - rs3113674 4:102957235 T 55024 NM_017935.4 Transcript intron_variant - - - - - - rs3113674 4:102957235 T CCDS47116.1 CCDS47116.1 Transcript intron_variant - - - - - - rs3113674 4:102957235 T CCDS34038.1 CCDS34038.1 Transcript intron_variant - - - - - - rs3113674 4:102957235 T ENSESTG00000015732 ENSESTT00000039432 Transcript intron_variant - - - - - - rs3113674 4:102957235 T 55024 NM_001083907.2 Transcript intron_variant - - - - - - rs3113674 4:102957235 T ENSESTG00000015899 ENSESTT00000039881 Transcript intron_variant - - - - - - rs236757 4:103056343 G - - - intergenic_variant - - - - - - rs230524 4:103459888 A ENSESTG00000015762 ENSESTT00000039570 Transcript intron_variant - - - - - - rs230524 4:103459888 A ENSESTG00000015762 ENSESTT00000039587 Transcript intron_variant - - - - - - rs230524 4:103459888 A ENSESTG00000015762 ENSESTT00000039598 Transcript intron_variant - - - - - - rs230524 4:103459888 A CCDS54783.1 CCDS54783.1 Transcript intron_variant - - - - - - rs230524 4:103459888 A 4790 NM_003998.3 Transcript intron_variant - - - - - - rs230524 4:103459888 A CCDS3657.1 CCDS3657.1 Transcript intron_variant - - - - - - rs230524 4:103459888 A 4790 NM_001165412.1 Transcript intron_variant - - - - - - rs230524 4:103459888 A ENSESTG00000015762 ENSESTT00000039583 Transcript intron_variant - - - - - - rs230524 4:103459888 A ENSESTG00000015762 ENSESTT00000039557 Transcript intron_variant - - - - - - rs230546 4:103509950 C ENSESTG00000015762 ENSESTT00000039570 Transcript intron_variant - - - - - - rs230546 4:103509950 C ENSESTG00000015762 ENSESTT00000039587 Transcript intron_variant - - - - - - rs230546 4:103509950 C ENSESTG00000015762 ENSESTT00000039598 Transcript intron_variant - - - - - - rs230546 4:103509950 C CCDS54783.1 CCDS54783.1 Transcript intron_variant - - - - - - rs230546 4:103509950 C 4790 NM_003998.3 Transcript intron_variant - - - - - - rs230546 4:103509950 C ENSESTG00000015762 ENSESTT00000039614 Transcript upstream_gene_variant - - - - - - DISTANCE=4128 rs230546 4:103509950 C CCDS3657.1 CCDS3657.1 Transcript intron_variant - - - - - - rs230546 4:103509950 C 4790 NM_001165412.1 Transcript intron_variant - - - - - - rs230546 4:103509950 C ENSESTG00000015762 ENSESTT00000039583 Transcript intron_variant - - - - - - rs230546 4:103509950 C ENSESTG00000015762 ENSESTT00000039557 Transcript intron_variant - - - - - - rs230546 4:103509950 C ENSESTG00000015762 ENSESTT00000039605 Transcript intron_variant - - - - - - rs228621 4:103571378 T ENSESTG00000016055 ENSESTT00000040295 Transcript intron_variant - - - - - - rs228621 4:103571378 T CCDS3658.1 CCDS3658.1 Transcript intron_variant - - - - - - rs228621 4:103571378 T ENSESTG00000016055 ENSESTT00000040276 Transcript intron_variant - - - - - - rs228621 4:103571378 T 4126 NM_005908.3 Transcript intron_variant - - - - - - rs228622 4:103571427 A ENSESTG00000016055 ENSESTT00000040295 Transcript intron_variant - - - - - - rs228622 4:103571427 A CCDS3658.1 CCDS3658.1 Transcript intron_variant - - - - - - rs228622 4:103571427 A ENSESTG00000016055 ENSESTT00000040276 Transcript intron_variant - - - - - - rs228622 4:103571427 A 4126 NM_005908.3 Transcript intron_variant - - - - - - rs4395509 4:104458438 G - - - intergenic_variant - - - - - - rs1354088 4:105009717 G - - - intergenic_variant - - - - - - rs6818748 4:105036600 C - - - intergenic_variant - - - - - - rs1295518 4:105200753 A - - - intergenic_variant - - - - - - rs3017673 4:105438861 G - - - intergenic_variant - - - - - - rs4499700 4:105797413 G - - - intergenic_variant - - - - - - rs1602295 4:105972920 G - - - intergenic_variant - - - - - - rs6847204 4:106159644 A ENSESTG00000004237 ENSESTT00000010690 Transcript intron_variant - - - - - - rs6847204 4:106159644 A CCDS3666.1 CCDS3666.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1047 rs6847204 4:106159644 A ENSESTG00000004237 ENSESTT00000010676 Transcript downstream_gene_variant - - - - - - DISTANCE=4228 rs6847204 4:106159644 A CCDS47120.1 CCDS47120.1 Transcript intron_variant - - - - - - rs6847204 4:106159644 A ENSESTG00000004237 ENSESTT00000010683 Transcript intron_variant - - - - - - rs6847204 4:106159644 A 54790 NM_001127208.2 Transcript intron_variant - - - - - - rs6847204 4:106159644 A 54790 NM_017628.4 Transcript 3_prime_UTR_variant 4949 - - - - - rs10018885 4:106334402 C CCDS34043.1 CCDS34043.1 Transcript intron_variant - - - - - - rs10018885 4:106334402 C 27068 NM_176867.3 Transcript intron_variant - - - - - - rs10018885 4:106334402 C 27068 NM_176869.2 Transcript intron_variant - - - - - - rs10018885 4:106334402 C CCDS3667.1 CCDS3667.1 Transcript intron_variant - - - - - - rs10018885 4:106334402 C ENSESTG00000004262 ENSESTT00000010805 Transcript intron_variant - - - - - - rs10018885 4:106334402 C ENSESTG00000004262 ENSESTT00000010794 Transcript intron_variant - - - - - - rs10018885 4:106334402 C CCDS3668.2 CCDS3668.2 Transcript intron_variant - - - - - - rs10018885 4:106334402 C ENSESTG00000004262 ENSESTT00000010827 Transcript intron_variant - - - - - - rs10018885 4:106334402 C CCDS3669.2 CCDS3669.2 Transcript intron_variant - - - - - - rs10018885 4:106334402 C 27068 NM_006903.4 Transcript intron_variant - - - - - - rs10018885 4:106334402 C ENSESTG00000004262 ENSESTT00000010787 Transcript intron_variant - - - - - - rs10018885 4:106334402 C 27068 NM_176866.2 Transcript intron_variant - - - - - - rs6533206 4:106474096 C 54848 NM_017700.1 Transcript synonymous_variant 320 174 58 T acT/acC - rs6533206 4:106474096 C CCDS3670.1 CCDS3670.1 Transcript synonymous_variant 174 174 58 T acT/acC - rs6533206 4:106474096 C ENSESTG00000004252 ENSESTT00000010702 Transcript synonymous_variant 318 174 58 T acT/acC - rs6533206 4:106474096 C CCDS56338.1 CCDS56338.1 Transcript synonymous_variant 174 174 58 T acT/acC - rs6533206 4:106474096 C 54848 NM_001242729.1 Transcript synonymous_variant 320 174 58 T acT/acC - rs2553447 4:106696578 G ENSESTG00000004049 ENSESTT00000010255 Transcript intron_variant - - - - - - rs2553447 4:106696578 G ENSESTG00000004049 ENSESTT00000010253 Transcript intron_variant - - - - - - rs2553447 4:106696578 G 79807 NM_001031720.3 Transcript intron_variant - - - - - - rs2553447 4:106696578 G CCDS43257.1 CCDS43257.1 Transcript intron_variant - - - - - - rs2553447 4:106696578 G ENSESTG00000004049 ENSESTT00000010244 Transcript intron_variant - - - - - - rs2553447 4:106696578 G ENSESTG00000004049 ENSESTT00000010250 Transcript intron_variant - - - - - - rs2553447 4:106696578 G ENSESTG00000004049 ENSESTT00000010251 Transcript intron_variant - - - - - - rs2553447 4:106696578 G 79807 NM_024751.3 Transcript intron_variant - - - - - - rs2553447 4:106696578 G CCDS3672.2 CCDS3672.2 Transcript intron_variant - - - - - - rs2553447 4:106696578 G ENSESTG00000004049 ENSESTT00000010236 Transcript intron_variant - - - - - - rs2553447 4:106696578 G ENSESTG00000004049 ENSESTT00000010243 Transcript intron_variant - - - - - - rs2553447 4:106696578 G ENSESTG00000004049 ENSESTT00000010231 Transcript intron_variant - - - - - - rs11097922 4:107146016 C CCDS3673.1 CCDS3673.1 Transcript intron_variant - - - - - - rs11097922 4:107146016 C ENSESTG00000004163 ENSESTT00000010548 Transcript intron_variant - - - - - - rs11097922 4:107146016 C 93627 NM_001163436.1 Transcript intron_variant - - - - - - rs11097922 4:107146016 C CCDS54788.1 CCDS54788.1 Transcript intron_variant - - - - - - rs11097922 4:107146016 C 93627 NM_033115.3 Transcript intron_variant - - - - - - rs11097922 4:107146016 C CCDS54789.1 CCDS54789.1 Transcript intron_variant - - - - - - rs11097922 4:107146016 C 93627 NM_001163437.1 Transcript intron_variant - - - - - - rs11097922 4:107146016 C 93627 NM_001163435.1 Transcript intron_variant - - - - - - rs3133164 4:107238966 T - ENSR00001246845 RegulatoryFeature regulatory_region_variant - - - - - - rs3133164 4:107238966 T ENSESTG00000004113 ENSESTT00000010415 Transcript intron_variant - - - - - - rs3133164 4:107238966 T ENSESTG00000004113 ENSESTT00000010394 Transcript intron_variant - - - - - - rs3133164 4:107238966 T ENSESTG00000004143 ENSESTT00000010478 Transcript upstream_gene_variant - - - - - - DISTANCE=1589 rs3133164 4:107238966 T 9255 NM_001142416.1 Transcript intron_variant - - - - - - rs3133164 4:107238966 T ENSESTG00000004113 ENSESTT00000010416 Transcript intron_variant - - - - - - rs3133164 4:107238966 T 9255 NM_001142415.1 Transcript intron_variant - - - - - - rs3133164 4:107238966 T 93627 NM_001163436.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1105 rs3133164 4:107238966 T 93627 NM_033115.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1543 rs3133164 4:107238966 T ENSESTG00000004143 ENSESTT00000010476 Transcript upstream_gene_variant - - - - - - DISTANCE=1589 rs3133164 4:107238966 T 9255 NM_004757.3 Transcript intron_variant - - - - - - rs3133164 4:107238966 T CCDS47121.1 CCDS47121.1 Transcript intron_variant - - - - - - rs3133164 4:107238966 T 93627 NM_001163437.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1543 rs3133164 4:107238966 T 93627 NM_001163435.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1543 rs2686309 4:107503256 G - - - intergenic_variant - - - - - - rs2648029 4:107504756 A - ENSR00001433854 RegulatoryFeature regulatory_region_variant - - - - - - rs2648029 4:107504756 A - - - intergenic_variant - - - - - - rs10005230 4:107770556 T - - - intergenic_variant - - - - - - rs6533273 4:107773881 G - - - intergenic_variant - - - - - - rs1873859 4:108794905 T ENSESTG00000010431 ENSESTT00000026125 Transcript intron_variant - - - - - - rs1873859 4:108794905 T 166929 NM_001136258.1 Transcript intron_variant - - - - - - rs1873859 4:108794905 T ENSESTG00000010431 ENSESTT00000026136 Transcript intron_variant - - - - - - rs1873859 4:108794905 T ENSESTG00000010431 ENSESTT00000026138 Transcript intron_variant - - - - - - rs4413479 4:109132818 A - - - intergenic_variant - - - - - - rs10033952 4:109143525 A - - - intergenic_variant - - - - - - rs6836302 4:109196555 C - - - intergenic_variant - - - - - - rs2530586 4:109233321 A - - - intergenic_variant - - - - - - rs220635 4:109235277 A - - - intergenic_variant - - - - - - rs7677844 4:109291083 C - - - intergenic_variant - - - - - - rs6839606 4:109401084 G - - - intergenic_variant - - - - - - rs2575643 4:109575647 G 58505 NM_021227.3 Transcript intron_variant - - - - - - rs2575643 4:109575647 G CCDS58921.1 CCDS58921.1 Transcript intron_variant - - - - - - rs2575643 4:109575647 G ENSESTG00000006083 ENSESTT00000015398 Transcript intron_variant - - - - - - rs2575643 4:109575647 G 58505 NM_001267818.1 Transcript intron_variant - - - - - - rs2575643 4:109575647 G 58505 NM_001267817.1 Transcript intron_variant - - - - - - rs2575643 4:109575647 G CCDS3681.1 CCDS3681.1 Transcript intron_variant - - - - - - rs2575612 4:109577225 G 58505 NM_021227.3 Transcript intron_variant - - - - - - rs2575612 4:109577225 G CCDS58921.1 CCDS58921.1 Transcript intron_variant - - - - - - rs2575612 4:109577225 G ENSESTG00000006083 ENSESTT00000015398 Transcript intron_variant - - - - - - rs2575612 4:109577225 G 58505 NM_001267818.1 Transcript intron_variant - - - - - - rs2575612 4:109577225 G 58505 NM_001267817.1 Transcript intron_variant - - - - - - rs2575612 4:109577225 G CCDS3681.1 CCDS3681.1 Transcript intron_variant - - - - - - rs7669463 4:109719560 G - - - intergenic_variant - - - - - - rs6533387 4:109728081 T 84570 NR_045756.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3796 rs6533387 4:109728081 T 84570 NM_198721.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3796 rs1452696 4:109733814 A 84570 NR_045756.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs1452696 4:109733814 A ENSESTG00000006179 ENSESTT00000015547 Transcript downstream_gene_variant - - - - - - DISTANCE=1042 rs1452696 4:109733814 A ENSESTG00000006107 ENSESTT00000015403 Transcript upstream_gene_variant - - - - - - DISTANCE=1042 rs1452696 4:109733814 A CCDS43258.1 CCDS43258.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1269 rs1452696 4:109733814 A 84570 NM_198721.2 Transcript 3_prime_UTR_variant 3765 - - - - - rs7694093 4:109784920 G 84570 NR_045756.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs7694093 4:109784920 G ENSESTG00000006179 ENSESTT00000015547 Transcript upstream_gene_variant - - - - - - DISTANCE=2167 rs7694093 4:109784920 G CCDS58922.1 CCDS58922.1 Transcript intron_variant - - - - - - rs7694093 4:109784920 G 84570 NM_001256074.1 Transcript intron_variant - - - - - - rs7694093 4:109784920 G 84570 NM_032518.2 Transcript intron_variant - - - - - - rs7694093 4:109784920 G CCDS43259.1 CCDS43259.1 Transcript intron_variant - - - - - - rs7694093 4:109784920 G 84570 NM_198721.2 Transcript intron_variant - - - - - - rs7694093 4:109784920 G CCDS43258.1 CCDS43258.1 Transcript intron_variant - - - - - - rs6842943 4:110253611 G - - - intergenic_variant - - - - - - rs197216 4:110521516 A ENSESTG00000006164 ENSESTT00000015526 Transcript intron_variant - - - - - - rs197216 4:110521516 A 55013 NM_017918.4 Transcript intron_variant - - - - - - rs197216 4:110521516 A CCDS3683.2 CCDS3683.2 Transcript intron_variant - - - - - - rs7699171 4:110597542 A ENSESTG00000006164 ENSESTT00000015526 Transcript intron_variant - - - - - - rs7699171 4:110597542 A 55013 NM_017918.4 Transcript intron_variant - - - - - - rs7699171 4:110597542 A ENSESTG00000015504 ENSESTT00000038868 Transcript intron_variant - - - - - - rs7699171 4:110597542 A CCDS3683.2 CCDS3683.2 Transcript intron_variant - - - - - - rs7699171 4:110597542 A ENSESTG00000015504 ENSESTT00000038873 Transcript intron_variant - - - - - - rs7668040 4:110867327 C 1950 NM_001178130.1 Transcript intron_variant - - - - - - rs7668040 4:110867327 C 1950 NM_001178131.1 Transcript intron_variant - - - - - - rs7668040 4:110867327 C CCDS54794.1 CCDS54794.1 Transcript intron_variant - - - - - - rs7668040 4:110867327 C ENSESTG00000015587 ENSESTT00000039035 Transcript downstream_gene_variant - - - - - - DISTANCE=2261 rs7668040 4:110867327 C 1950 NM_001963.4 Transcript intron_variant - - - - - - rs7668040 4:110867327 C ENSESTG00000015601 ENSESTT00000039066 Transcript intron_variant - - - - - - rs7668040 4:110867327 C CCDS3689.1 CCDS3689.1 Transcript intron_variant - - - - - - rs7668040 4:110867327 C CCDS54795.1 CCDS54795.1 Transcript intron_variant - - - - - - rs7668040 4:110867327 C ENSESTG00000015587 ENSESTT00000039046 Transcript downstream_gene_variant - - - - - - DISTANCE=2201 rs524875 4:111467490 T ENSESTG00000015658 ENSESTT00000039298 Transcript intron_variant - - - - - - rs524875 4:111467490 T ENSESTG00000015658 ENSESTT00000039307 Transcript upstream_gene_variant - - - - - - DISTANCE=3102 rs524875 4:111467490 T 2028 NM_001977.3 Transcript intron_variant - - - - - - rs524875 4:111467490 T CCDS3691.1 CCDS3691.1 Transcript intron_variant - - - - - - rs1448800 4:111516222 C - - - intergenic_variant - - - - - - rs4404615 4:111767431 C - - - intergenic_variant - - - - - - rs7696657 4:111785507 T 100126354 NR_030643.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3704 rs79053455 4:111808345 C - - - intergenic_variant - - - - - - rs525294 4:111817911 T - - - intergenic_variant - - - - - - rs10034004 4:111886234 C - - - intergenic_variant - - - - - - rs560572 4:111906436 C - - - intergenic_variant - - - - - - rs2654738 4:112321753 C - - - intergenic_variant - - - - - - rs10002879 4:112501855 A - - - intergenic_variant - - - - - - rs326877 4:112732007 G - - - intergenic_variant - - - - - - rs1009476 4:113280814 G 80216 NM_001253884.1 Transcript intron_variant - - - - - - rs1009476 4:113280814 G 80216 NM_001102406.1 Transcript intron_variant - - - - - - rs1009476 4:113280814 G ENSESTG00000011357 ENSESTT00000028543 Transcript intron_variant - - - - - - rs1009476 4:113280814 G ENSESTG00000011357 ENSESTT00000028555 Transcript intron_variant - - - - - - rs1009476 4:113280814 G ENSESTG00000011357 ENSESTT00000028551 Transcript intron_variant - - - - - - rs1009476 4:113280814 G 80216 NM_025144.3 Transcript intron_variant - - - - - - rs4308425 4:113616857 T - - - intergenic_variant - - - - - - rs6831743 4:113649792 C - - - intergenic_variant - - - - - - rs9990946 4:114851585 C ENSESTG00000019744 ENSESTT00000049494 Transcript intron_variant - - - - - - rs9990946 4:114851585 C 79642 NM_024590.3 Transcript intron_variant - - - - - - rs9990946 4:114851585 C CCDS43264.1 CCDS43264.1 Transcript intron_variant - - - - - - rs6533745 4:114957480 T - - - intergenic_variant - - - - - - rs4311377 4:114992350 G - ENSR00001247814 RegulatoryFeature regulatory_region_variant - - - - - - rs4311377 4:114992350 G - MA0139.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_NAME=Jaspar_Matrix_CTCF:MA0139.1;HIGH_INF_POS=N rs4311377 4:114992350 G - - - intergenic_variant - - - - - - rs7437526 4:115516701 G ENSESTG00000020690 ENSESTT00000051855 Transcript downstream_gene_variant - - - - - - DISTANCE=3401 rs7437526 4:115516701 G ENSESTG00000020534 ENSESTT00000051500 Transcript upstream_gene_variant - - - - - - DISTANCE=3274 rs7437526 4:115516701 G ENSESTG00000020534 ENSESTT00000051479 Transcript upstream_gene_variant - - - - - - DISTANCE=3225 rs7437526 4:115516701 G 7368 NM_001128174.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2910 rs7655572 4:115517127 C - ENSR00001247872 RegulatoryFeature regulatory_region_variant - - - - - - rs7655572 4:115517127 C ENSESTG00000020690 ENSESTT00000051855 Transcript downstream_gene_variant - - - - - - DISTANCE=2975 rs7655572 4:115517127 C ENSESTG00000020534 ENSESTT00000051500 Transcript upstream_gene_variant - - - - - - DISTANCE=2848 rs7655572 4:115517127 C ENSESTG00000020534 ENSESTT00000051479 Transcript upstream_gene_variant - - - - - - DISTANCE=2799 rs7655572 4:115517127 C 7368 NM_001128174.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2484 rs6855128 4:116127679 G - - - intergenic_variant - - - - - - rs7435947 4:116305132 T - - - intergenic_variant - - - - - - rs2018884 4:116837773 C - - - intergenic_variant - - - - - - rs814384 4:116988022 C - ENSR00001247965 RegulatoryFeature regulatory_region_variant - - - - - - rs814384 4:116988022 C - - - intergenic_variant - - - - - - rs2892712 4:117412627 A - - - intergenic_variant - - - - - - rs1370735 4:118048218 C - - - intergenic_variant - - - - - - rs10011166 4:118314345 G - - - intergenic_variant - - - - - - rs7654469 4:118383154 G - - - intergenic_variant - - - - - - rs7692699 4:118628767 G - - - intergenic_variant - - - - - - rs6824718 4:119029069 C 9348 NM_004784.2 Transcript intron_variant - - - - - - rs6824718 4:119029069 C ENSESTG00000015367 ENSESTT00000038500 Transcript intron_variant - - - - - - rs6824718 4:119029069 C CCDS3708.1 CCDS3708.1 Transcript intron_variant - - - - - - rs705840 4:119244569 C 8492 NM_003619.3 Transcript intron_variant - - - - - - rs705840 4:119244569 C ENSESTG00000015459 ENSESTT00000038741 Transcript intron_variant - - - - - - rs705840 4:119244569 C CCDS3709.1 CCDS3709.1 Transcript intron_variant - - - - - - rs6821273 4:119324515 C - - - intergenic_variant - - - - - - rs11730052 4:119447270 G ENSESTG00000015435 ENSESTT00000038677 Transcript intron_variant - - - - - - rs11730052 4:119447270 G 645455 NR_003135.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs11730052 4:119447270 G ENSESTG00000015435 ENSESTT00000038682 Transcript intron_variant - - - - - - rs11730052 4:119447270 G ENSESTG00000015435 ENSESTT00000038648 Transcript intron_variant - - - - - - rs11730052 4:119447270 G ENSESTG00000015435 ENSESTT00000038665 Transcript intron_variant - - - - - - rs1993610 4:119977299 T ENSESTG00000033799 ENSESTT00000085445 Transcript intron_variant - - - - - - rs1993610 4:119977299 T 171024 NM_133477.2 Transcript intron_variant - - - - - - rs1993610 4:119977299 T CCDS34054.1 CCDS34054.1 Transcript intron_variant - - - - - - rs972296 4:120143544 G 54532 NM_019050.2 Transcript intron_variant - - - - - - rs4834764 4:120149961 G 54532 NM_019050.2 Transcript intron_variant - - - - - - rs2928992 4:120492899 C 8654 NM_033437.3 Transcript intron_variant - - - - - - rs2928992 4:120492899 C CCDS34055.1 CCDS34055.1 Transcript intron_variant - - - - - - rs2928992 4:120492899 C 8654 NM_001083.3 Transcript intron_variant - - - - - - rs2928992 4:120492899 C ENSESTG00000033907 ENSESTT00000085721 Transcript intron_variant - - - - - - rs2928992 4:120492899 C CCDS3713.1 CCDS3713.1 Transcript intron_variant - - - - - - rs2928992 4:120492899 C ENSESTG00000033907 ENSESTT00000085712 Transcript intron_variant - - - - - - rs2928992 4:120492899 C ENSESTG00000033907 ENSESTT00000085716 Transcript intron_variant - - - - - - rs2928992 4:120492899 C 8654 NM_033430.2 Transcript intron_variant - - - - - - rs7442123 4:120728959 A - - - intergenic_variant - - - - - - rs2644698 4:121502363 T - - - intergenic_variant - - - - - - rs1376105 4:121885958 T - ENSR00001248424 RegulatoryFeature regulatory_region_variant - - - - - - rs1376105 4:121885958 T - - - intergenic_variant - - - - - - rs10012799 4:121890818 C - - - intergenic_variant - - - - - - rs2390066 4:121905964 C - - - intergenic_variant - - - - - - rs7375385 4:123191258 T CCDS43267.1 CCDS43267.1 Transcript intron_variant - - - - - - rs7375385 4:123191258 T ENSESTG00000030486 ENSESTT00000076831 Transcript intron_variant - - - - - - rs7375385 4:123191258 T ENSESTG00000030486 ENSESTT00000076822 Transcript intron_variant - - - - - - rs7375385 4:123191258 T ENSESTG00000030486 ENSESTT00000076835 Transcript intron_variant - - - - - - rs7375385 4:123191258 T 84162 NM_015312.3 Transcript intron_variant - - - - - - rs1398560 4:123593383 G - ENSR00001248635 RegulatoryFeature regulatory_region_variant - - - - - - rs1398560 4:123593383 G - - - intergenic_variant - - - - - - rs309378 4:123672863 G - - - intergenic_variant - - - - - - rs308436 4:123772205 C ENSESTG00000026900 ENSESTT00000067818 Transcript intron_variant - - - - - - rs308436 4:123772205 C CCDS34059.1 CCDS34059.1 Transcript intron_variant - - - - - - rs308436 4:123772205 C 2247 NM_002006.4 Transcript intron_variant - - - - - - rs2589851 4:124534141 G ENSESTG00000027044 ENSESTT00000068138 Transcript intron_variant - - - - - - rs1519247 4:125005116 T ENSESTG00000031489 ENSESTT00000079433 Transcript intron_variant - - - - - - rs1465855 4:125101417 T ENSESTG00000031499 ENSESTT00000079443 Transcript downstream_gene_variant - - - - - - DISTANCE=4187 rs1465855 4:125101417 T ENSESTG00000031489 ENSESTT00000079433 Transcript intron_variant - - - - - - rs521879 4:125216992 T - - - intergenic_variant - - - - - - rs518114 4:125217416 T - - - intergenic_variant - - - - - - rs535672 4:125233441 T - - - intergenic_variant - - - - - - rs666818 4:125280045 T - - - intergenic_variant - - - - - - rs586772 4:125281591 G - - - intergenic_variant - - - - - - rs11735445 4:125325905 T - - - intergenic_variant - - - - - - rs10016277 4:125408030 C - - - intergenic_variant - - - - - - rs1498013 4:125667853 C - - - intergenic_variant - - - - - - rs1506349 4:126448391 T - - - intergenic_variant - - - - - - rs6830847 4:126571304 C - - - intergenic_variant - - - - - - rs2013840 4:126618572 A ENSESTG00000015867 ENSESTT00000039798 Transcript intron_variant - - - - - - rs9968303 4:126790330 G - - - intergenic_variant - - - - - - rs1506168 4:126836235 C - - - intergenic_variant - - - - - - rs11098845 4:126857266 G - - - intergenic_variant - - - - - - rs498052 4:127034271 T - - - intergenic_variant - - - - - - rs9996768 4:127213178 G - - - intergenic_variant - - - - - - rs981833 4:127696356 C - - - intergenic_variant - - - - - - rs7654876 4:127765859 C - - - intergenic_variant - - - - - - rs10007925 4:128415380 C - - - intergenic_variant - - - - - - rs1588786 4:128489373 A - - - intergenic_variant - - - - - - rs4263415 4:128607482 C CCDS34061.1 CCDS34061.1 Transcript intron_variant - - - - - - rs4263415 4:128607482 C ENSESTG00000015169 ENSESTT00000038021 Transcript upstream_gene_variant - - - - - - DISTANCE=1334 rs4263415 4:128607482 C 27152 NM_015693.3 Transcript intron_variant - - - - - - rs4263415 4:128607482 C ENSESTG00000015166 ENSESTT00000037941 Transcript 5_prime_UTR_variant 1024 - - - - - rs6840822 4:128634149 G CCDS34061.1 CCDS34061.1 Transcript intron_variant - - - - - - rs6840822 4:128634149 G ENSESTG00000015169 ENSESTT00000038021 Transcript intron_variant - - - - - - rs6840822 4:128634149 G 27152 NM_015693.3 Transcript intron_variant - - - - - - rs11098938 4:128724232 A CCDS3734.1 CCDS3734.1 Transcript intron_variant - - - - - - rs11098938 4:128724232 A ENSESTG00000015222 ENSESTT00000038306 Transcript upstream_gene_variant - - - - - - DISTANCE=2604 rs11098938 4:128724232 A ENSESTG00000015222 ENSESTT00000038216 Transcript intron_variant - - - - - - rs11098938 4:128724232 A ENSESTG00000015222 ENSESTT00000038157 Transcript downstream_gene_variant - - - - - - DISTANCE=1887 rs11098938 4:128724232 A ENSESTG00000015222 ENSESTT00000038295 Transcript upstream_gene_variant - - - - - - DISTANCE=930 rs11098938 4:128724232 A ENSESTG00000015222 ENSESTT00000038143 Transcript downstream_gene_variant - - - - - - DISTANCE=4454 rs11098938 4:128724232 A 22824 NM_014278.2 Transcript intron_variant - - - - - - rs4279228 4:128802681 A - ENSR00001249292 RegulatoryFeature regulatory_region_variant - - - - - - rs4279228 4:128802681 A ENSESTG00000015319 ENSESTT00000038422 Transcript intron_variant - - - - - - rs4279228 4:128802681 A CCDS54804.1 CCDS54804.1 Transcript upstream_gene_variant - - - - - - DISTANCE=398 rs4279228 4:128802681 A CCDS3735.1 CCDS3735.1 Transcript intron_variant - - - - - - rs4279228 4:128802681 A CCDS54803.1 CCDS54803.1 Transcript intron_variant - - - - - - rs4279228 4:128802681 A 10733 NM_001190799.1 Transcript intron_variant - - - - - - rs4279228 4:128802681 A 10733 NM_014264.4 Transcript intron_variant - - - - - - rs4279228 4:128802681 A 10733 NM_001190801.1 Transcript intron_variant - - - - - - rs4279228 4:128802681 A ENSESTG00000015319 ENSESTT00000038375 Transcript intron_variant - - - - - - rs290002 4:129238845 C - - - intergenic_variant - - - - - - rs1599993 4:130070038 T - - - intergenic_variant - - - - - - rs2391533 4:130754311 A - - - intergenic_variant - - - - - - rs2391547 4:130786115 C - - - intergenic_variant - - - - - - rs1507785 4:130879727 C - - - intergenic_variant - - - - - - rs4546257 4:130934604 T - - - intergenic_variant - - - - - - rs965102 4:130944648 A - - - intergenic_variant - - - - - - rs1507777 4:130952249 T - - - intergenic_variant - - - - - - rs4864406 4:131103946 C - - - intergenic_variant - - - - - - rs1979688 4:131105624 A - - - intergenic_variant - - - - - - rs994891 4:131753714 T - - - intergenic_variant - - - - - - rs899123 4:131773009 A - - - intergenic_variant - - - - - - rs1304157 4:131797046 G - - - intergenic_variant - - - - - - rs10030831 4:131801789 G ENSESTG00000034858 ENSESTT00000088115 Transcript downstream_gene_variant - - - - - - DISTANCE=412 rs7671738 4:132181128 A - - - intergenic_variant - - - - - - rs8180289 4:132289095 C - - - intergenic_variant - - - - - - rs1911880 4:132309446 G - - - intergenic_variant - - - - - - rs1500781 4:132483037 C - - - intergenic_variant - - - - - - rs350976 4:132506427 T - - - intergenic_variant - - - - - - rs350977 4:132509933 G - - - intergenic_variant - - - - - - rs350969 4:132538504 T - - - intergenic_variant - - - - - - rs6534852 4:132557952 G - - - intergenic_variant - - - - - - rs349844 4:132799356 T - - - intergenic_variant - - - - - - rs348065 4:133114410 T - - - intergenic_variant - - - - - - rs348077 4:133130271 G - - - intergenic_variant - - - - - - rs6845745 4:133538955 A - - - intergenic_variant - - - - - - rs4640686 4:133691102 A - - - intergenic_variant - - - - - - rs6858308 4:133708315 A - - - intergenic_variant - - - - - - rs6830867 4:133711457 A - - - intergenic_variant - - - - - - rs11946027 4:134473185 A - - - intergenic_variant - - - - - - rs2713258 4:134627331 A - - - intergenic_variant - - - - - - rs4522918 4:135448698 T - - - intergenic_variant - - - - - - rs4241955 4:135640192 G - - - intergenic_variant - - - - - - rs4241957 4:135923255 G ENSESTG00000016788 ENSESTT00000042167 Transcript intron_variant - - - - - - rs4518309 4:136017244 C ENSESTG00000016788 ENSESTT00000042141 Transcript intron_variant - - - - - - rs4518309 4:136017244 C ENSESTG00000016788 ENSESTT00000042132 Transcript intron_variant - - - - - - rs4518309 4:136017244 C ENSESTG00000016774 ENSESTT00000042107 Transcript upstream_gene_variant - - - - - - DISTANCE=922 rs4863929 4:136026970 T ENSESTG00000016788 ENSESTT00000042141 Transcript intron_variant - - - - - - rs4863929 4:136026970 T ENSESTG00000016788 ENSESTT00000042132 Transcript intron_variant - - - - - - rs4385127 4:136034087 A ENSESTG00000016881 ENSESTT00000042353 Transcript downstream_gene_variant - - - - - - DISTANCE=187 rs4385127 4:136034087 A ENSESTG00000016788 ENSESTT00000042141 Transcript intron_variant - - - - - - rs4385127 4:136034087 A ENSESTG00000016788 ENSESTT00000042132 Transcript intron_variant - - - - - - rs6830600 4:136043458 T ENSESTG00000016881 ENSESTT00000042353 Transcript intron_variant - - - - - - rs6830600 4:136043458 T ENSESTG00000016881 ENSESTT00000042350 Transcript downstream_gene_variant - - - - - - DISTANCE=1173 rs6830600 4:136043458 T ENSESTG00000016788 ENSESTT00000042141 Transcript intron_variant - - - - - - rs6830600 4:136043458 T ENSESTG00000016788 ENSESTT00000042132 Transcript intron_variant - - - - - - rs4496631 4:136045832 C ENSESTG00000016881 ENSESTT00000042353 Transcript upstream_gene_variant - - - - - - DISTANCE=940 rs4496631 4:136045832 C ENSESTG00000016881 ENSESTT00000042350 Transcript upstream_gene_variant - - - - - - DISTANCE=898 rs4496631 4:136045832 C ENSESTG00000016788 ENSESTT00000042141 Transcript intron_variant - - - - - - rs4496631 4:136045832 C ENSESTG00000016788 ENSESTT00000042132 Transcript intron_variant - - - - - - rs1903344 4:136177056 A - - - intergenic_variant - - - - - - rs1460688 4:136201692 T - - - intergenic_variant - - - - - - rs1917951 4:136997137 C - - - intergenic_variant - - - - - - rs6844535 4:137390529 T - - - intergenic_variant - - - - - - rs10004781 4:137539943 T - - - intergenic_variant - - - - - - rs494539 4:137862880 C ENSESTG00000033686 ENSESTT00000085143 Transcript intron_variant - - - - - - rs1378875 4:137997403 T ENSESTG00000033686 ENSESTT00000085143 Transcript intron_variant - - - - - - rs10027915 4:138475925 G ENSESTG00000026137 ENSESTT00000065863 Transcript intron_variant - - - - - - rs10027915 4:138475925 G ENSESTG00000033678 ENSESTT00000085127 Transcript intron_variant - - - - - - rs7691643 4:138730538 C ENSESTG00000026144 ENSESTT00000065883 Transcript intron_variant - - - - - - rs1349346 4:139499930 C - - - intergenic_variant - - - - - - rs4367223 4:139715389 C - - - intergenic_variant - - - - - - rs4863491 4:139901057 A - - - intergenic_variant - - - - - - rs6811935 4:139932416 T CCDS3743.1 CCDS3743.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4720 rs6811935 4:139932416 T 25819 NM_012118.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4527 rs4863628 4:140005294 G - ENSR00001250235 RegulatoryFeature regulatory_region_variant - - - - - - rs4863628 4:140005294 G ENSESTG00000006521 ENSESTT00000016412 Transcript intron_variant - - - - - - rs4863628 4:140005294 G 1998 NM_006874.2 Transcript synonymous_variant 354 51 17 I atT/atC - rs4863628 4:140005294 G 1998 NM_201999.1 Transcript intron_variant - - - - - - rs4863628 4:140005294 G ENSESTG00000006603 ENSESTT00000016701 Transcript synonymous_variant 341 51 17 I atT/atC - rs4863628 4:140005294 G ENSESTG00000006603 ENSESTT00000016697 Transcript intron_variant - - - - - - rs4863628 4:140005294 G CCDS3745.1 CCDS3745.1 Transcript synonymous_variant 51 51 17 I atT/atC - rs4863628 4:140005294 G ENSESTG00000006603 ENSESTT00000016681 Transcript intron_variant - - - - - - rs4863628 4:140005294 G ENSESTG00000006603 ENSESTT00000016691 Transcript intron_variant - - - - - - rs4863628 4:140005294 G CCDS3744.1 CCDS3744.1 Transcript intron_variant - - - - - - rs4863628 4:140005294 G ENSESTG00000006603 ENSESTT00000016699 Transcript synonymous_variant 341 51 17 I atT/atC - rs4863628 4:140005294 G ENSESTG00000006603 ENSESTT00000016684 Transcript intron_variant - - - - - - rs6535881 4:140011445 T ENSESTG00000006603 ENSESTT00000016697 Transcript intron_variant - - - - - - rs6535881 4:140011445 T 1998 NM_201999.1 Transcript intron_variant - - - - - - rs6535881 4:140011445 T ENSESTG00000006603 ENSESTT00000016691 Transcript intron_variant - - - - - - rs6535881 4:140011445 T ENSESTG00000006603 ENSESTT00000016681 Transcript intron_variant - - - - - - rs6535881 4:140011445 T CCDS3744.1 CCDS3744.1 Transcript intron_variant - - - - - - rs6535881 4:140011445 T ENSESTG00000006603 ENSESTT00000016684 Transcript intron_variant - - - - - - rs7660579 4:140033822 T ENSESTG00000006603 ENSESTT00000016697 Transcript intron_variant - - - - - - rs7660579 4:140033822 T ENSESTG00000006523 ENSESTT00000016419 Transcript upstream_gene_variant - - - - - - DISTANCE=2056 rs7660579 4:140033822 T 1998 NM_201999.1 Transcript intron_variant - - - - - - rs7660579 4:140033822 T ENSESTG00000006603 ENSESTT00000016691 Transcript intron_variant - - - - - - rs7660579 4:140033822 T ENSESTG00000006603 ENSESTT00000016681 Transcript intron_variant - - - - - - rs7660579 4:140033822 T CCDS3744.1 CCDS3744.1 Transcript intron_variant - - - - - - rs7660579 4:140033822 T ENSESTG00000006603 ENSESTT00000016684 Transcript intron_variant - - - - - - rs13149976 4:140037219 A ENSESTG00000006603 ENSESTT00000016697 Transcript intron_variant - - - - - - rs13149976 4:140037219 A ENSESTG00000006523 ENSESTT00000016419 Transcript downstream_gene_variant - - - - - - DISTANCE=825 rs13149976 4:140037219 A 1998 NM_201999.1 Transcript intron_variant - - - - - - rs13149976 4:140037219 A ENSESTG00000006603 ENSESTT00000016691 Transcript intron_variant - - - - - - rs13149976 4:140037219 A ENSESTG00000006603 ENSESTT00000016681 Transcript intron_variant - - - - - - rs13149976 4:140037219 A CCDS3744.1 CCDS3744.1 Transcript intron_variant - - - - - - rs13149976 4:140037219 A ENSESTG00000006603 ENSESTT00000016684 Transcript intron_variant - - - - - - rs6844698 4:140061315 T 1998 NM_201999.1 Transcript upstream_gene_variant - - - - - - DISTANCE=709 rs6844698 4:140061315 T ENSESTG00000006603 ENSESTT00000016691 Transcript intron_variant - - - - - - rs6844698 4:140061315 T ENSESTG00000006603 ENSESTT00000016681 Transcript intron_variant - - - - - - rs6844698 4:140061315 T CCDS3744.1 CCDS3744.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2460 rs6844698 4:140061315 T ENSESTG00000006603 ENSESTT00000016684 Transcript intron_variant - - - - - - rs11100417 4:140917812 T CCDS54805.1 CCDS54805.1 Transcript intron_variant - - - - - - rs11100417 4:140917812 T 55534 NM_018717.4 Transcript intron_variant - - - - - - rs11100417 4:140917812 T ENSESTG00000014847 ENSESTT00000037164 Transcript intron_variant - - - - - - rs4241934 4:141059404 G CCDS54805.1 CCDS54805.1 Transcript intron_variant - - - - - - rs4241934 4:141059404 G 55534 NM_018717.4 Transcript intron_variant - - - - - - rs4241934 4:141059404 G ENSESTG00000014772 ENSESTT00000036936 Transcript downstream_gene_variant - - - - - - DISTANCE=3685 rs4241934 4:141059404 G ENSESTG00000014772 ENSESTT00000036944 Transcript downstream_gene_variant - - - - - - DISTANCE=1471 rs2668574 4:141292768 A CCDS3750.1 CCDS3750.1 Transcript intron_variant - - - - - - rs2668574 4:141292768 A 60592 NM_032547.2 Transcript intron_variant - - - - - - rs2668574 4:141292768 A CCDS54807.1 CCDS54807.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1923 rs2668574 4:141292768 A ENSESTG00000014775 ENSESTT00000037012 Transcript upstream_gene_variant - - - - - - DISTANCE=2029 rs2668574 4:141292768 A 60592 NM_001153635.1 Transcript intron_variant - - - - - - rs2668574 4:141292768 A 60592 NM_001153585.1 Transcript intron_variant - - - - - - rs2668574 4:141292768 A 60592 NM_001153552.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1896 rs2668574 4:141292768 A 100129858 NR_033939.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2668574 4:141292768 A 60592 NM_001153690.1 Transcript intron_variant - - - - - - rs2668574 4:141292768 A ENSESTG00000014775 ENSESTT00000037021 Transcript upstream_gene_variant - - - - - - DISTANCE=4807 rs2668574 4:141292768 A 60592 NM_001153663.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1896 rs2668574 4:141292768 A 60592 NM_001153446.1 Transcript intron_variant - - - - - - rs2668574 4:141292768 A CCDS54806.1 CCDS54806.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1923 rs2668574 4:141292768 A 60592 NM_001153484.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1896 rs1241051 4:141398233 T ENSESTG00000014795 ENSESTT00000037071 Transcript intron_variant - - - - - - rs1241051 4:141398233 T ENSESTG00000019576 ENSESTT00000049124 Transcript intron_variant - - - - - - rs1241051 4:141398233 T ENSESTG00000014795 ENSESTT00000037057 Transcript intron_variant - - - - - - rs1241051 4:141398233 T ENSESTG00000019576 ENSESTT00000049100 Transcript intron_variant - - - - - - rs1241051 4:141398233 T ENSESTG00000014795 ENSESTT00000037050 Transcript intron_variant - - - - - - rs1241049 4:141404326 A ENSESTG00000014795 ENSESTT00000037071 Transcript intron_variant - - - - - - rs1241049 4:141404326 A ENSESTG00000019576 ENSESTT00000049124 Transcript intron_variant - - - - - - rs1241049 4:141404326 A ENSESTG00000014795 ENSESTT00000037057 Transcript intron_variant - - - - - - rs1241049 4:141404326 A ENSESTG00000019576 ENSESTT00000049100 Transcript intron_variant - - - - - - rs1241049 4:141404326 A ENSESTG00000014795 ENSESTT00000037050 Transcript intron_variant - - - - - - rs7678800 4:141443205 C ENSESTG00000019268 ENSESTT00000048504 Transcript upstream_gene_variant - - - - - - DISTANCE=4591 rs7678800 4:141443205 C ENSESTG00000019268 ENSESTT00000048485 Transcript upstream_gene_variant - - - - - - DISTANCE=2112 rs7678800 4:141443205 C 255520 NM_153702.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2107 rs7678800 4:141443205 C CCDS3752.1 CCDS3752.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3378 rs1471919 4:141761847 C - - - intergenic_variant - - - - - - rs6823805 4:141886640 A CCDS34065.1 CCDS34065.1 Transcript intron_variant - - - - - - rs6823805 4:141886640 A 57484 NM_020724.1 Transcript intron_variant - - - - - - rs6823805 4:141886640 A ENSESTG00000019400 ENSESTT00000048815 Transcript intron_variant - - - - - - rs6823805 4:141886640 A ENSESTG00000019400 ENSESTT00000048826 Transcript intron_variant - - - - - - rs10004747 4:141962912 C CCDS34065.1 CCDS34065.1 Transcript intron_variant - - - - - - rs10004747 4:141962912 C 57484 NM_020724.1 Transcript intron_variant - - - - - - rs10004747 4:141962912 C ENSESTG00000019400 ENSESTT00000048815 Transcript intron_variant - - - - - - rs10004747 4:141962912 C ENSESTG00000019400 ENSESTT00000048826 Transcript intron_variant - - - - - - rs6537059 4:142639110 G ENSESTG00000029562 ENSESTT00000074502 Transcript intron_variant - - - - - - rs6537059 4:142639110 G 3600 NM_172175.2 Transcript intron_variant - - - - - - rs6537059 4:142639110 G ENSESTG00000029562 ENSESTT00000074520 Transcript intron_variant - - - - - - rs6537059 4:142639110 G ENSESTG00000029562 ENSESTT00000074533 Transcript upstream_gene_variant - - - - - - DISTANCE=1174 rs6537059 4:142639110 G 3600 NR_037840.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs6537059 4:142639110 G ENSESTG00000029562 ENSESTT00000074540 Transcript upstream_gene_variant - - - - - - DISTANCE=3825 rs6537059 4:142639110 G CCDS3755.1 CCDS3755.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1508 rs6537059 4:142639110 G CCDS3756.1 CCDS3756.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3192 rs6537059 4:142639110 G 3600 NM_000585.4 Transcript intron_variant - - - - - - rs184595 4:143012992 C - ENSR00001435718 RegulatoryFeature regulatory_region_variant - - - - - - rs184595 4:143012992 C 8821 NM_001101669.1 Transcript intron_variant - - - - - - rs184595 4:143012992 C 8821 NM_003866.2 Transcript intron_variant - - - - - - rs184595 4:143012992 C CCDS3757.1 CCDS3757.1 Transcript intron_variant - - - - - - rs336335 4:143030917 A 8821 NM_001101669.1 Transcript intron_variant - - - - - - rs336335 4:143030917 A 8821 NM_003866.2 Transcript intron_variant - - - - - - rs336335 4:143030917 A CCDS3757.1 CCDS3757.1 Transcript intron_variant - - - - - - rs1559710 4:143520240 A 8821 NM_001101669.1 Transcript intron_variant - - - - - - rs1559710 4:143520240 A 8821 NM_003866.2 Transcript intron_variant - - - - - - rs7686725 4:143526854 C 8821 NM_001101669.1 Transcript intron_variant - - - - - - rs7686725 4:143526854 C 8821 NM_003866.2 Transcript intron_variant - - - - - - rs1373042 4:143550344 A 8821 NM_001101669.1 Transcript intron_variant - - - - - - rs1373042 4:143550344 A 8821 NM_003866.2 Transcript intron_variant - - - - - - rs1397110 4:143886415 A - - - intergenic_variant - - - - - - rs6537138 4:143909127 G - - - intergenic_variant - - - - - - rs4481200 4:143922158 G - - - intergenic_variant - - - - - - rs1901080 4:144573252 G - ENSR00001250973 RegulatoryFeature regulatory_region_variant - - - - - - rs1901080 4:144573252 G CCDS54808.1 CCDS54808.1 Transcript intron_variant - - - - - - rs1901080 4:144573252 G 166752 NM_001168235.1 Transcript intron_variant - - - - - - rs1901080 4:144573252 G ENSESTG00000018458 ENSESTT00000046442 Transcript intron_variant - - - - - - rs1901080 4:144573252 G ENSESTG00000018174 ENSESTT00000045765 Transcript downstream_gene_variant - - - - - - DISTANCE=2793 rs6537182 4:144681010 A - - - intergenic_variant - - - - - - rs4054636 4:144708253 T - - - intergenic_variant - - - - - - rs2719337 4:145367123 A - - - intergenic_variant - - - - - - rs2657805 4:145381520 G - - - intergenic_variant - - - - - - rs1512289 4:145387723 A - - - intergenic_variant - - - - - - rs1844430 4:145501201 C - ENSR00001251080 RegulatoryFeature regulatory_region_variant - - - - - - rs1844430 4:145501201 C - - - intergenic_variant - - - - - - rs2575578 4:145667225 T - - - intergenic_variant - - - - - - rs1390982 4:146565344 G ENSESTG00000020793 ENSESTT00000052152 Transcript intron_variant - - - - - - rs1390982 4:146565344 G CCDS3766.1 CCDS3766.1 Transcript intron_variant - - - - - - rs1390982 4:146565344 G 166785 NM_172250.2 Transcript intron_variant - - - - - - rs7656294 4:146605044 T CCDS47140.1 CCDS47140.1 Transcript intron_variant - - - - - - rs7656294 4:146605044 T 646603 NM_001080531.1 Transcript intron_variant - - - - - - rs7656294 4:146605044 T ENSESTG00000020825 ENSESTT00000052298 Transcript intron_variant - - - - - - rs2356562 4:146739979 G 152485 NM_178835.3 Transcript intron_variant - - - - - - rs2356562 4:146739979 G ENSESTG00000021252 ENSESTT00000053441 Transcript intron_variant - - - - - - rs2356562 4:146739979 G CCDS34072.1 CCDS34072.1 Transcript intron_variant - - - - - - rs1426885 4:146946504 C - - - intergenic_variant - - - - - - rs4561946 4:147298897 C ENSESTG00000021086 ENSESTT00000053033 Transcript intron_variant - - - - - - rs4561946 4:147298897 C CCDS34073.1 CCDS34073.1 Transcript intron_variant - - - - - - rs4561946 4:147298897 C 84068 NM_001029998.3 Transcript intron_variant - - - - - - rs905712 4:147628903 T ENSESTG00000027645 ENSESTT00000069578 Transcript downstream_gene_variant - - - - - - DISTANCE=197 rs905712 4:147628903 T ENSESTG00000027722 ENSESTT00000069807 Transcript intron_variant - - - - - - rs905712 4:147628903 T CCDS47141.1 CCDS47141.1 Transcript intron_variant - - - - - - rs905712 4:147628903 T ENSESTG00000027722 ENSESTT00000069866 Transcript intron_variant - - - - - - rs905712 4:147628903 T ENSESTG00000027722 ENSESTT00000069858 Transcript intron_variant - - - - - - rs905712 4:147628903 T 83894 NM_031956.2 Transcript intron_variant - - - - - - rs2655616 4:147635982 T ENSESTG00000027722 ENSESTT00000069807 Transcript intron_variant - - - - - - rs2655616 4:147635982 T CCDS47141.1 CCDS47141.1 Transcript intron_variant - - - - - - rs2655616 4:147635982 T ENSESTG00000027722 ENSESTT00000069866 Transcript intron_variant - - - - - - rs2655616 4:147635982 T ENSESTG00000027722 ENSESTT00000069858 Transcript intron_variant - - - - - - rs2655616 4:147635982 T 83894 NM_031956.2 Transcript intron_variant - - - - - - rs1509334 4:147849975 T ENSESTG00000027674 ENSESTT00000069751 Transcript intron_variant - - - - - - rs1509334 4:147849975 T CCDS47141.1 CCDS47141.1 Transcript intron_variant - - - - - - rs1509334 4:147849975 T ENSESTG00000027674 ENSESTT00000069732 Transcript intron_variant - - - - - - rs1509334 4:147849975 T ENSESTG00000027649 ENSESTT00000069590 Transcript intron_variant - - - - - - rs1509334 4:147849975 T 83894 NM_031956.2 Transcript intron_variant - - - - - - rs1911586 4:148136171 G - - - intergenic_variant - - - - - - rs4392492 4:148147274 G - - - intergenic_variant - - - - - - rs10011341 4:148185805 G - - - intergenic_variant - - - - - - rs1594083 4:148334247 T - - - intergenic_variant - - - - - - rs4835400 4:148362222 T - - - intergenic_variant - - - - - - rs4835090 4:148539615 C 55751 NM_018241.2 Transcript intron_variant - - - - - - rs4835090 4:148539615 C CCDS3770.1 CCDS3770.1 Transcript intron_variant - - - - - - rs2654935 4:148560357 T - ENSR00001436039 RegulatoryFeature regulatory_region_variant - - - - - - rs2654935 4:148560357 T ENSESTG00000031704 ENSESTT00000080063 Transcript intron_variant - - - - - - rs2654935 4:148560357 T ENSESTG00000031571 ENSESTT00000079653 Transcript downstream_gene_variant - - - - - - DISTANCE=4565 rs2654935 4:148560357 T 90826 NM_138364.2 Transcript intron_variant - - - - - - rs2654935 4:148560357 T 55751 NM_018241.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3683 rs2654935 4:148560357 T CCDS3770.1 CCDS3770.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4772 rs2654935 4:148560357 T ENSESTG00000031571 ENSESTT00000079663 Transcript downstream_gene_variant - - - - - - DISTANCE=4565 rs2654935 4:148560357 T ENSESTG00000031704 ENSESTT00000080054 Transcript intron_variant - - - - - - rs2654935 4:148560357 T CCDS3771.1 CCDS3771.1 Transcript intron_variant - - - - - - rs7664148 4:148613942 T - - - intergenic_variant - - - - - - rs6854186 4:148648595 G 79658 NM_024605.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4858 rs6854186 4:148648595 G CCDS34075.1 CCDS34075.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4858 rs6854186 4:148648595 G ENSESTG00000031593 ENSESTT00000079678 Transcript upstream_gene_variant - - - - - - DISTANCE=4619 rs905605 4:148651122 G 79658 NM_024605.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2331 rs905605 4:148651122 G CCDS34075.1 CCDS34075.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2331 rs905605 4:148651122 G ENSESTG00000031593 ENSESTT00000079678 Transcript upstream_gene_variant - - - - - - DISTANCE=2092 rs4835450 4:148662383 A 79658 NM_024605.3 Transcript intron_variant - - - - - - rs4835450 4:148662383 A CCDS34075.1 CCDS34075.1 Transcript intron_variant - - - - - - rs4835450 4:148662383 A ENSESTG00000031593 ENSESTT00000079678 Transcript intron_variant - - - - - - rs6823034 4:148669245 G 79658 NM_024605.3 Transcript intron_variant - - - - - - rs6823034 4:148669245 G CCDS34075.1 CCDS34075.1 Transcript intron_variant - - - - - - rs6823034 4:148669245 G ENSESTG00000031593 ENSESTT00000079678 Transcript intron_variant - - - - - - rs924782 4:148678794 C 79658 NM_024605.3 Transcript intron_variant - - - - - - rs924782 4:148678794 C CCDS34075.1 CCDS34075.1 Transcript intron_variant - - - - - - rs924782 4:148678794 C ENSESTG00000031593 ENSESTT00000079678 Transcript intron_variant - - - - - - rs4835466 4:148787275 C - ENSR00001251562 RegulatoryFeature regulatory_region_variant - - - - - - rs4835466 4:148787275 C ENSESTG00000031600 ENSESTT00000079729 Transcript intron_variant - - - - - - rs4835466 4:148787275 C 79658 NM_024605.3 Transcript intron_variant - - - - - - rs4835466 4:148787275 C CCDS34075.1 CCDS34075.1 Transcript intron_variant - - - - - - rs6535570 4:148808350 C ENSESTG00000031600 ENSESTT00000079729 Transcript intron_variant - - - - - - rs6535570 4:148808350 C 79658 NM_024605.3 Transcript intron_variant - - - - - - rs6535570 4:148808350 C CCDS34075.1 CCDS34075.1 Transcript intron_variant - - - - - - rs349023 4:148838285 T ENSESTG00000031600 ENSESTT00000079729 Transcript downstream_gene_variant - - - - - - DISTANCE=3994 rs349023 4:148838285 T 79658 NM_024605.3 Transcript intron_variant - - - - - - rs349023 4:148838285 T CCDS34075.1 CCDS34075.1 Transcript intron_variant - - - - - - rs168368 4:148866242 G 79658 NM_024605.3 Transcript intron_variant - - - - - - rs168368 4:148866242 G CCDS34075.1 CCDS34075.1 Transcript intron_variant - - - - - - rs1436491 4:148872981 C 79658 NM_024605.3 Transcript intron_variant - - - - - - rs1436491 4:148872981 C CCDS34075.1 CCDS34075.1 Transcript intron_variant - - - - - - rs3843412 4:149097211 G ENSESTG00000031645 ENSESTT00000079849 Transcript intron_variant - - - - - - rs3843412 4:149097211 G CCDS54811.1 CCDS54811.1 Transcript intron_variant - - - - - - rs3843412 4:149097211 G 4306 NM_000901.4 Transcript intron_variant - - - - - - rs3843412 4:149097211 G ENSESTG00000031645 ENSESTT00000079864 Transcript intron_variant - - - - - - rs3843412 4:149097211 G 4306 NM_001166104.1 Transcript intron_variant - - - - - - rs3843412 4:149097211 G ENSESTG00000031638 ENSESTT00000079811 Transcript intron_variant - - - - - - rs3843412 4:149097211 G CCDS3772.1 CCDS3772.1 Transcript intron_variant - - - - - - rs4621409 4:149107547 T ENSESTG00000031645 ENSESTT00000079849 Transcript intron_variant - - - - - - rs4621409 4:149107547 T CCDS54811.1 CCDS54811.1 Transcript intron_variant - - - - - - rs4621409 4:149107547 T 4306 NM_000901.4 Transcript intron_variant - - - - - - rs4621409 4:149107547 T ENSESTG00000031645 ENSESTT00000079864 Transcript intron_variant - - - - - - rs4621409 4:149107547 T 4306 NM_001166104.1 Transcript intron_variant - - - - - - rs4621409 4:149107547 T ENSESTG00000031638 ENSESTT00000079811 Transcript intron_variant - - - - - - rs4621409 4:149107547 T CCDS3772.1 CCDS3772.1 Transcript intron_variant - - - - - - rs3846314 4:149159180 A - ENSR00001436097 RegulatoryFeature regulatory_region_variant - - - - - - rs3846314 4:149159180 A ENSESTG00000031645 ENSESTT00000079849 Transcript intron_variant - - - - - - rs3846314 4:149159180 A CCDS54811.1 CCDS54811.1 Transcript intron_variant - - - - - - rs3846314 4:149159180 A 4306 NM_000901.4 Transcript intron_variant - - - - - - rs3846314 4:149159180 A 4306 NM_001166104.1 Transcript intron_variant - - - - - - rs3846314 4:149159180 A ENSESTG00000031645 ENSESTT00000079858 Transcript intron_variant - - - - - - rs3846314 4:149159180 A CCDS3772.1 CCDS3772.1 Transcript intron_variant - - - - - - rs3846330 4:149235083 G ENSESTG00000031645 ENSESTT00000079849 Transcript intron_variant - - - - - - rs3846330 4:149235083 G CCDS54811.1 CCDS54811.1 Transcript intron_variant - - - - - - rs3846330 4:149235083 G 4306 NM_000901.4 Transcript intron_variant - - - - - - rs3846330 4:149235083 G 4306 NM_001166104.1 Transcript intron_variant - - - - - - rs3846330 4:149235083 G ENSESTG00000031645 ENSESTT00000079858 Transcript intron_variant - - - - - - rs3846330 4:149235083 G CCDS3772.1 CCDS3772.1 Transcript intron_variant - - - - - - rs1033123 4:149286293 A ENSESTG00000031645 ENSESTT00000079849 Transcript intron_variant - - - - - - rs1033123 4:149286293 A CCDS54811.1 CCDS54811.1 Transcript intron_variant - - - - - - rs1033123 4:149286293 A 4306 NM_000901.4 Transcript intron_variant - - - - - - rs1033123 4:149286293 A 4306 NM_001166104.1 Transcript intron_variant - - - - - - rs1033123 4:149286293 A ENSESTG00000031645 ENSESTT00000079858 Transcript intron_variant - - - - - - rs1033123 4:149286293 A CCDS3772.1 CCDS3772.1 Transcript intron_variant - - - - - - rs1398267 4:149342222 C ENSESTG00000031645 ENSESTT00000079849 Transcript intron_variant - - - - - - rs1398267 4:149342222 C CCDS54811.1 CCDS54811.1 Transcript intron_variant - - - - - - rs1398267 4:149342222 C 4306 NM_000901.4 Transcript intron_variant - - - - - - rs1398267 4:149342222 C 4306 NM_001166104.1 Transcript intron_variant - - - - - - rs1398267 4:149342222 C CCDS3772.1 CCDS3772.1 Transcript intron_variant - - - - - - rs2358464 4:149573021 A - - - intergenic_variant - - - - - - rs4368583 4:150033755 C - - - intergenic_variant - - - - - - rs540545 4:150140049 G - - - intergenic_variant - - - - - - rs533769 4:150186498 A - - - intergenic_variant - - - - - - rs484393 4:150200415 A - - - intergenic_variant - - - - - - rs13149505 4:150240877 A - - - intergenic_variant - - - - - - rs4530612 4:150287825 A ENSESTG00000021176 ENSESTT00000053176 Transcript intron_variant - - - - - - rs10019350 4:150371056 T 285423 XM_003403498.1 Transcript intron_variant - - - - - - rs10019350 4:150371056 T ENSESTG00000021176 ENSESTT00000053176 Transcript intron_variant - - - - - - rs1503692 4:150411490 A 285423 XM_003403498.1 Transcript intron_variant - - - - - - rs1503692 4:150411490 A ENSESTG00000021176 ENSESTT00000053176 Transcript intron_variant - - - - - - rs1503706 4:150442527 T 285423 XM_003403498.1 Transcript intron_variant - - - - - - rs1503706 4:150442527 T ENSESTG00000021176 ENSESTT00000053176 Transcript intron_variant - - - - - - rs1827558 4:150453607 C 285423 XM_003403498.1 Transcript intron_variant - - - - - - rs1827558 4:150453607 C ENSESTG00000021176 ENSESTT00000053176 Transcript intron_variant - - - - - - rs1503698 4:150490234 G 285423 XM_003403498.1 Transcript intron_variant - - - - - - rs1032824 4:150502512 T 285423 XM_003403498.1 Transcript intron_variant - - - - - - rs1847357 4:150503731 T 285423 XM_003403498.1 Transcript intron_variant - - - - - - rs980751 4:150508527 C 285423 XM_003403498.1 Transcript intron_variant - - - - - - rs980751 4:150508527 C ENSESTG00000012551 ENSESTT00000031482 Transcript downstream_gene_variant - - - - - - DISTANCE=568 rs1148653 4:151799699 A CCDS58928.1 CCDS58928.1 Transcript intron_variant - - - - - - rs1148653 4:151799699 A 987 NM_001199282.2 Transcript intron_variant - - - - - - rs1148653 4:151799699 A ENSESTG00000005167 ENSESTT00000013119 Transcript intron_variant - - - - - - rs1148653 4:151799699 A CCDS3773.1 CCDS3773.1 Transcript intron_variant - - - - - - rs1148653 4:151799699 A 987 NM_006726.4 Transcript intron_variant - - - - - - rs361172 4:152784535 C - - - intergenic_variant - - - - - - rs7664610 4:152927018 C - - - intergenic_variant - - - - - - rs4696338 4:153608140 A - - - intergenic_variant - - - - - - rs1844671 4:155227182 T CCDS3785.1 CCDS3785.1 Transcript intron_variant - - - - - - rs1844671 4:155227182 T 54798 NM_017639.3 Transcript intron_variant - - - - - - rs7689660 4:155528972 A ENSESTG00000012615 ENSESTT00000031681 Transcript intron_variant - - - - - - rs7689660 4:155528972 A 2266 NM_000509.4 Transcript intron_variant - - - - - - rs7689660 4:155528972 A ENSESTG00000012615 ENSESTT00000031714 Transcript intron_variant - - - - - - rs7689660 4:155528972 A CCDS3788.1 CCDS3788.1 Transcript intron_variant - - - - - - rs7689660 4:155528972 A ENSESTG00000012615 ENSESTT00000031733 Transcript intron_variant - - - - - - rs7689660 4:155528972 A CCDS47153.1 CCDS47153.1 Transcript intron_variant - - - - - - rs7689660 4:155528972 A ENSESTG00000012615 ENSESTT00000031688 Transcript intron_variant - - - - - - rs7689660 4:155528972 A ENSESTG00000012615 ENSESTT00000031744 Transcript intron_variant - - - - - - rs7689660 4:155528972 A ENSESTG00000012615 ENSESTT00000031725 Transcript intron_variant - - - - - - rs7689660 4:155528972 A 2266 NM_021870.2 Transcript intron_variant - - - - - - rs5000433 4:155531740 A - ENSR00001252560 RegulatoryFeature regulatory_region_variant - - - - - - rs5000433 4:155531740 A ENSESTG00000012615 ENSESTT00000031681 Transcript intron_variant - - - - - - rs5000433 4:155531740 A 2266 NM_000509.4 Transcript intron_variant - - - - - - rs5000433 4:155531740 A ENSESTG00000012615 ENSESTT00000031714 Transcript intron_variant - - - - - - rs5000433 4:155531740 A CCDS3788.1 CCDS3788.1 Transcript intron_variant - - - - - - rs5000433 4:155531740 A ENSESTG00000012615 ENSESTT00000031733 Transcript intron_variant - - - - - - rs5000433 4:155531740 A CCDS47153.1 CCDS47153.1 Transcript intron_variant - - - - - - rs5000433 4:155531740 A ENSESTG00000012615 ENSESTT00000031688 Transcript intron_variant - - - - - - rs5000433 4:155531740 A ENSESTG00000012615 ENSESTT00000031744 Transcript intron_variant - - - - - - rs5000433 4:155531740 A ENSESTG00000012615 ENSESTT00000031725 Transcript intron_variant - - - - - - rs5000433 4:155531740 A 2266 NM_021870.2 Transcript intron_variant - - - - - - rs10028717 4:155548920 T ENSESTG00000012557 ENSESTT00000031499 Transcript intron_variant - - - - - - rs10028717 4:155548920 T ENSESTG00000012557 ENSESTT00000031492 Transcript intron_variant - - - - - - rs1902486 4:155855695 C - - - intergenic_variant - - - - - - rs1902485 4:155882488 C - ENSR00001252600 RegulatoryFeature regulatory_region_variant - - - - - - rs1902485 4:155882488 C - - - intergenic_variant - - - - - - rs7665741 4:155970962 T - - - intergenic_variant - - - - - - rs12508947 4:156270989 G ENSESTG00000012585 ENSESTT00000031559 Transcript upstream_gene_variant - - - - - - DISTANCE=4379 rs12508947 4:156270989 G ENSESTG00000012589 ENSESTT00000031594 Transcript intron_variant - - - - - - rs12508947 4:156270989 G ENSESTG00000012576 ENSESTT00000031553 Transcript downstream_gene_variant - - - - - - DISTANCE=3437 rs12508947 4:156270989 G 79884 NM_001039580.1 Transcript intron_variant - - - - - - rs12508947 4:156270989 G CCDS35493.1 CCDS35493.1 Transcript intron_variant - - - - - - rs12508947 4:156270989 G ENSESTG00000012589 ENSESTT00000031599 Transcript intron_variant - - - - - - rs1032052 4:156485269 C - - - intergenic_variant - - - - - - rs6812987 4:156950239 T - - - intergenic_variant - - - - - - rs7674242 4:156950766 A - - - intergenic_variant - - - - - - rs12711306 4:157045369 T - - - intergenic_variant - - - - - - rs6536189 4:157447720 A - - - intergenic_variant - - - - - - rs1364905 4:157773770 T 56034 NR_036641.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1364905 4:157773770 T 56034 NM_016205.2 Transcript intron_variant - - - - - - rs1364905 4:157773770 T ENSESTG00000027128 ENSESTT00000068378 Transcript intron_variant - - - - - - rs1364905 4:157773770 T CCDS3795.1 CCDS3795.1 Transcript intron_variant - - - - - - rs1364905 4:157773770 T ENSESTG00000027128 ENSESTT00000068404 Transcript intron_variant - - - - - - rs1826209 4:158536111 C - - - intergenic_variant - - - - - - rs4691421 4:158537021 T - - - intergenic_variant - - - - - - rs4690894 4:159121777 T ENSESTG00000000141 ENSESTT00000000376 Transcript downstream_gene_variant - - - - - - DISTANCE=1790 rs4690894 4:159121777 T ENSESTG00000000141 ENSESTT00000000374 Transcript downstream_gene_variant - - - - - - DISTANCE=1174 rs6536321 4:159351761 A - - - intergenic_variant - - - - - - rs7375436 4:159411979 G - - - intergenic_variant - - - - - - rs6841826 4:159449358 T ENSESTG00000019311 ENSESTT00000048642 Transcript intron_variant - - - - - - rs6841826 4:159449358 T 59350 NM_021634.3 Transcript intron_variant - - - - - - rs6841826 4:159449358 T 59350 NR_045581.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6841826 4:159449358 T CCDS43276.1 CCDS43276.1 Transcript intron_variant - - - - - - rs6841826 4:159449358 T CCDS58929.1 CCDS58929.1 Transcript intron_variant - - - - - - rs6841826 4:159449358 T 59350 NM_001253730.1 Transcript intron_variant - - - - - - rs6841826 4:159449358 T 59350 NR_045580.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6841826 4:159449358 T 59350 NM_001253728.1 Transcript intron_variant - - - - - - rs6841826 4:159449358 T 59350 NM_001253729.1 Transcript intron_variant - - - - - - rs6841826 4:159449358 T ENSESTG00000019311 ENSESTT00000048671 Transcript intron_variant - - - - - - rs6841826 4:159449358 T 59350 NM_001253727.1 Transcript intron_variant - - - - - - rs6841826 4:159449358 T ENSESTG00000019311 ENSESTT00000048686 Transcript intron_variant - - - - - - rs6841826 4:159449358 T 59350 NR_045582.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6841826 4:159449358 T 59350 NR_045583.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6841826 4:159449358 T 59350 NR_045579.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6841826 4:159449358 T CCDS58930.1 CCDS58930.1 Transcript intron_variant - - - - - - rs6841826 4:159449358 T ENSESTG00000019311 ENSESTT00000048629 Transcript intron_variant - - - - - - rs6841826 4:159449358 T 59350 NR_045584.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6841826 4:159449358 T 59350 NM_001253732.1 Transcript intron_variant - - - - - - rs6841826 4:159449358 T 59350 NM_001253733.1 Transcript intron_variant - - - - - - rs6841826 4:159449358 T ENSESTG00000019311 ENSESTT00000048613 Transcript intron_variant - - - - - - rs6536356 4:159578391 T 59350 NM_001253729.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NM_001253727.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NM_021634.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NR_045582.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NR_045581.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NR_045583.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NR_045579.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NM_001253733.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NM_001253732.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NM_001253730.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NR_045580.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs6536356 4:159578391 T 59350 NM_001253728.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3867 rs10213546 4:159683163 G - - - intergenic_variant - - - - - - rs7675609 4:159694876 G ENSESTG00000019580 ENSESTT00000049296 Transcript intron_variant - - - - - - rs7675609 4:159694876 G 57600 NM_020840.1 Transcript intron_variant - - - - - - rs7675609 4:159694876 G CCDS47155.1 CCDS47155.1 Transcript intron_variant - - - - - - rs7675609 4:159694876 G ENSESTG00000019580 ENSESTT00000049351 Transcript intron_variant - - - - - - rs10007888 4:159713085 A ENSESTG00000019580 ENSESTT00000049296 Transcript intron_variant - - - - - - rs10007888 4:159713085 A 57600 NM_020840.1 Transcript intron_variant - - - - - - rs10007888 4:159713085 A CCDS47155.1 CCDS47155.1 Transcript intron_variant - - - - - - rs10007888 4:159713085 A ENSESTG00000019580 ENSESTT00000049351 Transcript intron_variant - - - - - - rs4690913 4:159825191 C CCDS47156.1 CCDS47156.1 Transcript intron_variant - - - - - - rs4690913 4:159825191 C 57600 NM_020840.1 Transcript intron_variant - - - - - - rs4690913 4:159825191 C CCDS47155.1 CCDS47155.1 Transcript intron_variant - - - - - - rs4690913 4:159825191 C ENSESTG00000019701 ENSESTT00000049457 Transcript intron_variant - - - - - - rs4690913 4:159825191 C 152940 NM_152543.2 Transcript intron_variant - - - - - - rs595471 4:159903111 G CCDS47156.1 CCDS47156.1 Transcript intron_variant - - - - - - rs595471 4:159903111 G ENSESTG00000020201 ENSESTT00000050640 Transcript intron_variant - - - - - - rs595471 4:159903111 G 152940 NM_152543.2 Transcript intron_variant - - - - - - rs10018684 4:159917202 T CCDS47156.1 CCDS47156.1 Transcript intron_variant - - - - - - rs10018684 4:159917202 T ENSESTG00000020201 ENSESTT00000050640 Transcript intron_variant - - - - - - rs10018684 4:159917202 T 152940 NM_152543.2 Transcript intron_variant - - - - - - rs672256 4:159943226 G CCDS47156.1 CCDS47156.1 Transcript intron_variant - - - - - - rs672256 4:159943226 G ENSESTG00000020201 ENSESTT00000050645 Transcript synonymous_variant 196 117 39 H caT/caC - rs672256 4:159943226 G ENSESTG00000020201 ENSESTT00000050640 Transcript intron_variant - - - - - - rs672256 4:159943226 G 152940 NM_152543.2 Transcript intron_variant - - - - - - rs603458 4:159960282 G CCDS47156.1 CCDS47156.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4034 rs603458 4:159960282 G ENSESTG00000020201 ENSESTT00000050645 Transcript upstream_gene_variant - - - - - - DISTANCE=3955 rs603458 4:159960282 G ENSESTG00000020201 ENSESTT00000050640 Transcript upstream_gene_variant - - - - - - DISTANCE=3949 rs603458 4:159960282 G 152940 NM_152543.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3949 rs4691545 4:160103946 C - - - intergenic_variant - - - - - - rs4690936 4:160226896 C ENSESTG00000019796 ENSESTT00000050005 Transcript intron_variant - - - - - - rs4690936 4:160226896 C ENSESTG00000019796 ENSESTT00000050058 Transcript intron_variant - - - - - - rs4690936 4:160226896 C ENSESTG00000019796 ENSESTT00000049976 Transcript intron_variant - - - - - - rs4690936 4:160226896 C CCDS43277.1 CCDS43277.1 Transcript intron_variant - - - - - - rs4690936 4:160226896 C ENSESTG00000019796 ENSESTT00000049990 Transcript intron_variant - - - - - - rs4690936 4:160226896 C ENSESTG00000019796 ENSESTT00000049949 Transcript intron_variant - - - - - - rs4690936 4:160226896 C ENSESTG00000019796 ENSESTT00000049917 Transcript intron_variant - - - - - - rs4690936 4:160226896 C 9693 NM_014247.2 Transcript intron_variant - - - - - - rs4690936 4:160226896 C ENSESTG00000019796 ENSESTT00000050036 Transcript intron_variant - - - - - - rs4690936 4:160226896 C ENSESTG00000019796 ENSESTT00000050051 Transcript intron_variant - - - - - - rs4690936 4:160226896 C ENSESTG00000019796 ENSESTT00000049930 Transcript intron_variant - - - - - - rs6536410 4:160237904 A ENSESTG00000019796 ENSESTT00000050005 Transcript intron_variant - - - - - - rs6536410 4:160237904 A ENSESTG00000019796 ENSESTT00000050058 Transcript intron_variant - - - - - - rs6536410 4:160237904 A ENSESTG00000019796 ENSESTT00000049976 Transcript intron_variant - - - - - - rs6536410 4:160237904 A CCDS43277.1 CCDS43277.1 Transcript intron_variant - - - - - - rs6536410 4:160237904 A ENSESTG00000019796 ENSESTT00000049990 Transcript intron_variant - - - - - - rs6536410 4:160237904 A ENSESTG00000019796 ENSESTT00000049949 Transcript intron_variant - - - - - - rs6536410 4:160237904 A ENSESTG00000019796 ENSESTT00000049917 Transcript intron_variant - - - - - - rs6536410 4:160237904 A 9693 NM_014247.2 Transcript intron_variant - - - - - - rs6536410 4:160237904 A ENSESTG00000019796 ENSESTT00000050036 Transcript intron_variant - - - - - - rs6536410 4:160237904 A ENSESTG00000019796 ENSESTT00000050051 Transcript intron_variant - - - - - - rs6536410 4:160237904 A ENSESTG00000019796 ENSESTT00000049930 Transcript intron_variant - - - - - - rs1815924 4:160422423 C - - - intergenic_variant - - - - - - rs7696865 4:160553833 T - - - intergenic_variant - - - - - - rs10017955 4:160603836 C - - - intergenic_variant - - - - - - rs1119631 4:160620409 T - - - intergenic_variant - - - - - - rs2348636 4:160767328 T - - - intergenic_variant - - - - - - rs4690964 4:160817414 T - - - intergenic_variant - - - - - - rs2349524 4:161062325 C - - - intergenic_variant - - - - - - rs10015262 4:161198960 G - - - intergenic_variant - - - - - - rs7654242 4:161232029 C - - - intergenic_variant - - - - - - rs1371258 4:161374056 A - - - intergenic_variant - - - - - - rs6536523 4:161442294 T - - - intergenic_variant - - - - - - rs4691705 4:161749156 A - - - intergenic_variant - - - - - - rs4365680 4:161978292 G - - - intergenic_variant - - - - - - rs4279164 4:161983735 A - - - intergenic_variant - - - - - - rs4452387 4:161990939 C - - - intergenic_variant - - - - - - rs4475100 4:162006880 C - - - intergenic_variant - - - - - - rs4234939 4:162019399 G - - - intergenic_variant - - - - - - rs2918994 4:162057415 C - - - intergenic_variant - - - - - - rs670282 4:162091170 T - - - intergenic_variant - - - - - - rs2313432 4:162295024 T - - - intergenic_variant - - - - - - rs359120 4:162761118 T CCDS3802.1 CCDS3802.1 Transcript intron_variant - - - - - - rs359120 4:162761118 T CCDS47158.1 CCDS47158.1 Transcript intron_variant - - - - - - rs359120 4:162761118 T ENSESTG00000004201 ENSESTT00000010614 Transcript intron_variant - - - - - - rs359120 4:162761118 T 56884 NM_001128428.2 Transcript intron_variant - - - - - - rs359120 4:162761118 T 56884 NM_001128427.2 Transcript intron_variant - - - - - - rs359120 4:162761118 T 56884 NM_020116.4 Transcript intron_variant - - - - - - rs359120 4:162761118 T CCDS47157.1 CCDS47157.1 Transcript intron_variant - - - - - - rs359120 4:162761118 T ENSESTG00000004201 ENSESTT00000010606 Transcript intron_variant - - - - - - rs958986 4:163051192 C 56884 NM_020116.4 Transcript intron_variant - - - - - - rs958986 4:163051192 C ENSESTG00000004201 ENSESTT00000010614 Transcript intron_variant - - - - - - rs958986 4:163051192 C ENSESTG00000004201 ENSESTT00000010606 Transcript intron_variant - - - - - - rs958986 4:163051192 C 56884 NM_001128428.2 Transcript intron_variant - - - - - - rs958986 4:163051192 C 56884 NM_001128427.2 Transcript intron_variant - - - - - - rs13136184 4:163217624 G - - - intergenic_variant - - - - - - rs195926 4:163602523 C - ENSR00001253371 RegulatoryFeature regulatory_region_variant - - - - - - rs195926 4:163602523 C - - - intergenic_variant - - - - - - rs11729729 4:163621537 G - - - intergenic_variant - - - - - - rs2061865 4:163963825 G - - - intergenic_variant - - - - - - rs4565037 4:164229762 G - - - intergenic_variant - - - - - - rs4146927 4:164269478 A CCDS3804.1 CCDS3804.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1948 rs4146927 4:164269478 A ENSESTG00000028050 ENSESTT00000070599 Transcript upstream_gene_variant - - - - - - DISTANCE=1937 rs4146927 4:164269478 A ENSESTG00000028050 ENSESTT00000070583 Transcript intron_variant - - - - - - rs4146927 4:164269478 A 4889 NM_006174.2 Transcript intron_variant - - - - - - rs517566 4:166838664 T 7092 NM_012464.4 Transcript intron_variant - - - - - - rs517566 4:166838664 T ENSESTG00000008275 ENSESTT00000020879 Transcript intron_variant - - - - - - rs517566 4:166838664 T ENSESTG00000008275 ENSESTT00000020874 Transcript intron_variant - - - - - - rs517566 4:166838664 T CCDS56342.1 CCDS56342.1 Transcript intron_variant - - - - - - rs517566 4:166838664 T 7092 NM_001204760.1 Transcript intron_variant - - - - - - rs517566 4:166838664 T CCDS3811.1 CCDS3811.1 Transcript intron_variant - - - - - - rs11100628 4:166900038 A 7092 NM_012464.4 Transcript intron_variant - - - - - - rs11100628 4:166900038 A ENSESTG00000008275 ENSESTT00000020879 Transcript intron_variant - - - - - - rs11100628 4:166900038 A ENSESTG00000008275 ENSESTT00000020874 Transcript intron_variant - - - - - - rs11100628 4:166900038 A CCDS56342.1 CCDS56342.1 Transcript intron_variant - - - - - - rs11100628 4:166900038 A 7092 NM_001204760.1 Transcript intron_variant - - - - - - rs11100628 4:166900038 A CCDS3811.1 CCDS3811.1 Transcript intron_variant - - - - - - rs1497950 4:167024479 T ENSESTG00000008298 ENSESTT00000020926 Transcript upstream_gene_variant - - - - - - DISTANCE=3781 rs1497950 4:167024479 T 7092 NM_012464.4 Transcript 3_prime_UTR_variant 6140 - - - - - rs1497950 4:167024479 T ENSESTG00000008290 ENSESTT00000020918 Transcript downstream_gene_variant - - - - - - DISTANCE=327 rs1497950 4:167024479 T CCDS3811.1 CCDS3811.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2451 rs56928352 4:167106685 C - - - intergenic_variant - - - - - - rs2201815 4:167112119 T - - - intergenic_variant - - - - - - rs353875 4:167115612 G - - - intergenic_variant - - - - - - rs168496 4:167117650 T - - - intergenic_variant - - - - - - rs400071 4:167200625 T - - - intergenic_variant - - - - - - rs2703837 4:167922550 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs2703837 4:167922550 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs2703837 4:167922550 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs2703837 4:167922550 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs1365945 4:167925666 G 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G 50859 NM_016950.2 Transcript intron_variant - - - - - - rs1365945 4:167925666 G 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs1365945 4:167925666 G CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs2558140 4:167931836 A 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A 50859 NM_016950.2 Transcript intron_variant - - - - - - rs2558140 4:167931836 A 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs2558140 4:167931836 A CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs11132853 4:167969820 G 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G 50859 NM_016950.2 Transcript intron_variant - - - - - - rs11132853 4:167969820 G 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs11132853 4:167969820 G CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs10000380 4:167972636 A 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A 50859 NM_016950.2 Transcript intron_variant - - - - - - rs10000380 4:167972636 A 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs10000380 4:167972636 A CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs6839300 4:167987418 T 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T 50859 NM_016950.2 Transcript intron_variant - - - - - - rs6839300 4:167987418 T 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs6839300 4:167987418 T CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs6853805 4:167990364 A 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A 50859 NM_016950.2 Transcript intron_variant - - - - - - rs6853805 4:167990364 A 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs6853805 4:167990364 A CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A - ENSR00001437205 RegulatoryFeature regulatory_region_variant - - - - - - rs6810884 4:167990753 A CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs6810884 4:167990753 A 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A 50859 NM_016950.2 Transcript intron_variant - - - - - - rs6810884 4:167990753 A 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs6810884 4:167990753 A CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs10050157 4:167992328 T 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T 50859 NM_016950.2 Transcript intron_variant - - - - - - rs10050157 4:167992328 T 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs10050157 4:167992328 T CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs6819117 4:167992390 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs6819117 4:167992390 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs6819117 4:167992390 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs6553541 4:167995735 A 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A 50859 NM_016950.2 Transcript intron_variant - - - - - - rs6553541 4:167995735 A 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs6553541 4:167995735 A CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs1863784 4:168010823 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs1863784 4:168010823 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs1863784 4:168010823 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815214 4:168033804 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815214 4:168033804 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C CCDS56344.1 CCDS56344.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815214 4:168033804 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs1834832 4:168048201 T 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T 50859 NM_016950.2 Transcript intron_variant - - - - - - rs1834832 4:168048201 T 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs1834832 4:168048201 T CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs1427628 4:168051687 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs1427628 4:168051687 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs1427628 4:168051687 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815238 4:168056529 A 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815238 4:168056529 A 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815238 4:168056529 A CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815236 4:168057561 A 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815236 4:168057561 A 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815236 4:168057561 A CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815234 4:168061089 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815234 4:168061089 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815234 4:168061089 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815231 4:168063633 G 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815231 4:168063633 G 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815231 4:168063633 G CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815230 4:168065164 T 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815230 4:168065164 T 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815230 4:168065164 T CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815229 4:168066023 T 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815229 4:168066023 T 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815229 4:168066023 T CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs1093054 4:168067850 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs1093054 4:168067850 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs1093054 4:168067850 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815223 4:168074404 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815223 4:168074404 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815223 4:168074404 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815221 4:168075121 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815221 4:168075121 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815221 4:168075121 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C CCDS58931.1 CCDS58931.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C ENSESTG00000026454 ENSESTT00000066747 Transcript intron_variant - - - - - - rs815220 4:168075327 C 50859 NM_001204355.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C 50859 NM_001204352.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C CCDS34095.1 CCDS34095.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C CCDS56345.1 CCDS56345.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C 50859 NM_001204354.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C 50859 NM_016950.2 Transcript intron_variant - - - - - - rs815220 4:168075327 C 50859 NM_001204353.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C 50859 NM_001204358.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C 50859 NM_001251967.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C 50859 NM_001204356.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C CCDS56346.1 CCDS56346.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C CCDS54817.1 CCDS54817.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C 50859 NM_001040159.1 Transcript intron_variant - - - - - - rs815220 4:168075327 C CCDS56347.1 CCDS56347.1 Transcript intron_variant - - - - - - rs6553897 4:168516173 C - - - intergenic_variant - - - - - - rs304363 4:168858113 T - - - intergenic_variant - - - - - - rs304362 4:168873171 T - - - intergenic_variant - - - - - - rs4476561 4:169022596 G ENSESTG00000012672 ENSESTT00000031854 Transcript intron_variant - - - - - - rs4476561 4:169022596 G CCDS34096.1 CCDS34096.1 Transcript intron_variant - - - - - - rs4476561 4:169022596 G ENSESTG00000012672 ENSESTT00000031851 Transcript intron_variant - - - - - - rs4476561 4:169022596 G 11199 NM_007193.4 Transcript intron_variant - - - - - - rs4692661 4:169336662 C 91351 NM_001012967.1 Transcript missense_variant 3097 2876 959 Y/C tAt/tGt - PolyPhen=benign;SIFT=tolerated rs4692661 4:169336662 C CCDS47161.1 CCDS47161.1 Transcript missense_variant 2876 2876 959 Y/C tAt/tGt - PolyPhen=benign;SIFT=tolerated rs4692661 4:169336662 C ENSESTG00000028573 ENSESTT00000071857 Transcript missense_variant 461 446 149 Y/C tAt/tGt - rs963114 4:169951245 C - - - intergenic_variant - - - - - - rs3966096 4:169959548 A - - - intergenic_variant - - - - - - rs2125321 4:169969935 T - - - intergenic_variant - - - - - - rs2706749 4:170136706 C CCDS34099.1 CCDS34099.1 Transcript intron_variant - - - - - - rs2706749 4:170136706 C ENSESTG00000028361 ENSESTT00000071467 Transcript intron_variant - - - - - - rs2706749 4:170136706 C ENSESTG00000028344 ENSESTT00000071272 Transcript upstream_gene_variant - - - - - - DISTANCE=1758 rs2706749 4:170136706 C ENSESTG00000028361 ENSESTT00000071493 Transcript intron_variant - - - - - - rs2706749 4:170136706 C 57630 NM_020870.3 Transcript intron_variant - - - - - - rs10018214 4:170426091 T CCDS56349.1 CCDS56349.1 Transcript intron_variant - - - - - - rs10018214 4:170426091 T CCDS47162.1 CCDS47162.1 Transcript intron_variant - - - - - - rs10018214 4:170426091 T 4750 NM_001199399.1 Transcript intron_variant - - - - - - rs10018214 4:170426091 T CCDS56351.1 CCDS56351.1 Transcript intron_variant - - - - - - rs10018214 4:170426091 T 4750 NM_001199397.1 Transcript intron_variant - - - - - - rs10018214 4:170426091 T 4750 NM_001199398.1 Transcript intron_variant - - - - - - rs10018214 4:170426091 T CCDS56348.1 CCDS56348.1 Transcript intron_variant - - - - - - rs10018214 4:170426091 T 4750 NM_012224.2 Transcript intron_variant - - - - - - rs10018214 4:170426091 T 4750 NM_001199400.1 Transcript intron_variant - - - - - - rs10018214 4:170426091 T CCDS56350.1 CCDS56350.1 Transcript intron_variant - - - - - - rs10016583 4:170481756 G ENSESTG00000008618 ENSESTT00000021674 Transcript downstream_gene_variant - - - - - - DISTANCE=1253 rs10016583 4:170481756 G CCDS56349.1 CCDS56349.1 Transcript intron_variant - - - - - - rs10016583 4:170481756 G CCDS47162.1 CCDS47162.1 Transcript intron_variant - - - - - - rs10016583 4:170481756 G 4750 NM_001199399.1 Transcript intron_variant - - - - - - rs10016583 4:170481756 G CCDS56351.1 CCDS56351.1 Transcript intron_variant - - - - - - rs10016583 4:170481756 G 4750 NM_001199397.1 Transcript intron_variant - - - - - - rs10016583 4:170481756 G 4750 NM_001199398.1 Transcript intron_variant - - - - - - rs10016583 4:170481756 G CCDS56348.1 CCDS56348.1 Transcript intron_variant - - - - - - rs10016583 4:170481756 G 4750 NM_012224.2 Transcript intron_variant - - - - - - rs10016583 4:170481756 G 4750 NM_001199400.1 Transcript intron_variant - - - - - - rs10016583 4:170481756 G CCDS56350.1 CCDS56350.1 Transcript intron_variant - - - - - - rs4692733 4:170506990 T ENSESTG00000008618 ENSESTT00000021674 Transcript upstream_gene_variant - - - - - - DISTANCE=401 rs4692733 4:170506990 T CCDS56349.1 CCDS56349.1 Transcript intron_variant - - - - - - rs4692733 4:170506990 T CCDS47162.1 CCDS47162.1 Transcript intron_variant - - - - - - rs4692733 4:170506990 T 4750 NM_001199399.1 Transcript intron_variant - - - - - - rs4692733 4:170506990 T CCDS56351.1 CCDS56351.1 Transcript intron_variant - - - - - - rs4692733 4:170506990 T ENSESTG00000008606 ENSESTT00000021640 Transcript intron_variant - - - - - - rs4692733 4:170506990 T ENSESTG00000008606 ENSESTT00000021642 Transcript intron_variant - - - - - - rs4692733 4:170506990 T 4750 NM_001199397.1 Transcript intron_variant - - - - - - rs4692733 4:170506990 T 4750 NM_001199398.1 Transcript intron_variant - - - - - - rs4692733 4:170506990 T CCDS56348.1 CCDS56348.1 Transcript intron_variant - - - - - - rs4692733 4:170506990 T 4750 NM_012224.2 Transcript intron_variant - - - - - - rs4692733 4:170506990 T 4750 NM_001199400.1 Transcript intron_variant - - - - - - rs4692733 4:170506990 T CCDS56350.1 CCDS56350.1 Transcript intron_variant - - - - - - rs2062610 4:170635603 T 1182 NM_173872.3 Transcript intron_variant - - - - - - rs2062610 4:170635603 T CCDS34100.1 CCDS34100.1 Transcript intron_variant - - - - - - rs2062610 4:170635603 T 1182 NM_001243374.1 Transcript intron_variant - - - - - - rs2062610 4:170635603 T ENSESTG00000008469 ENSESTT00000021353 Transcript downstream_gene_variant - - - - - - DISTANCE=723 rs2062610 4:170635603 T CCDS58932.1 CCDS58932.1 Transcript intron_variant - - - - - - rs2062610 4:170635603 T CCDS34101.1 CCDS34101.1 Transcript intron_variant - - - - - - rs2062610 4:170635603 T 1182 NM_001829.3 Transcript intron_variant - - - - - - rs2062610 4:170635603 T 1182 NM_001243372.1 Transcript intron_variant - - - - - - rs2062610 4:170635603 T ENSESTG00000008469 ENSESTT00000021348 Transcript intron_variant - - - - - - rs6846267 4:170710727 C - - - intergenic_variant - - - - - - rs6419976 4:170809966 A - - - intergenic_variant - - - - - - rs2332073 4:171810979 C - - - intergenic_variant - - - - - - rs10016670 4:172133310 G - - - intergenic_variant - - - - - - rs11132882 4:172135465 G - - - intergenic_variant - - - - - - rs4692632 4:172284685 C - - - intergenic_variant - - - - - - rs2332317 4:172443062 T - - - intergenic_variant - - - - - - rs2877655 4:172590458 G - - - intergenic_variant - - - - - - rs1587931 4:172936419 A CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs1587931 4:172936419 A 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs836315 4:173109642 C CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs836315 4:173109642 C 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs6553619 4:173216230 A CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs6553619 4:173216230 A 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs6553619 4:173216230 A ENSESTG00000016583 ENSESTT00000041589 Transcript intron_variant - - - - - - rs6553619 4:173216230 A ENSESTG00000016583 ENSESTT00000041575 Transcript intron_variant - - - - - - rs333394 4:173255221 A CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs333394 4:173255221 A 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs333394 4:173255221 A ENSESTG00000016583 ENSESTT00000041589 Transcript intron_variant - - - - - - rs333394 4:173255221 A ENSESTG00000016583 ENSESTT00000041575 Transcript intron_variant - - - - - - rs2332483 4:173287058 G CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs2332483 4:173287058 G 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs2332483 4:173287058 G ENSESTG00000016583 ENSESTT00000041589 Transcript intron_variant - - - - - - rs10031695 4:173289235 T CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs10031695 4:173289235 T 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs10031695 4:173289235 T ENSESTG00000016583 ENSESTT00000041589 Transcript intron_variant - - - - - - rs336004 4:173359287 C CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs336004 4:173359287 C 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs336004 4:173359287 C ENSESTG00000016583 ENSESTT00000041589 Transcript intron_variant - - - - - - rs338032 4:173404470 A CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs338032 4:173404470 A 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs338032 4:173404470 A ENSESTG00000016583 ENSESTT00000041589 Transcript intron_variant - - - - - - rs338038 4:173455376 G CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs338038 4:173455376 G 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs338038 4:173455376 G ENSESTG00000016583 ENSESTT00000041589 Transcript intron_variant - - - - - - rs338034 4:173474056 C CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs338034 4:173474056 C 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs1370573 4:173597523 A CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs1370573 4:173597523 A 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs11737728 4:173599924 G CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs11737728 4:173599924 G 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs7699541 4:173642749 T CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs7699541 4:173642749 T 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs1824346 4:173821562 C ENSESTG00000026094 ENSESTT00000065781 Transcript intron_variant - - - - - - rs1824346 4:173821562 C CCDS34104.1 CCDS34104.1 Transcript intron_variant - - - - - - rs1824346 4:173821562 C 442117 NM_001034845.2 Transcript intron_variant - - - - - - rs11721452 4:174293723 A 8819 NM_003864.3 Transcript intron_variant - - - - - - rs11721452 4:174293723 A ENSESTG00000001008 ENSESTT00000002451 Transcript intron_variant - - - - - - rs11721452 4:174293723 A ENSESTG00000001008 ENSESTT00000002433 Transcript downstream_gene_variant - - - - - - DISTANCE=1340 rs11721452 4:174293723 A CCDS3817.1 CCDS3817.1 Transcript intron_variant - - - - - - rs4695744 4:174729815 G - - - intergenic_variant - - - - - - rs4695746 4:174769394 A - - - intergenic_variant - - - - - - rs7690356 4:174777813 C - - - intergenic_variant - - - - - - rs4540017 4:174819268 C ENSESTG00000001060 ENSESTT00000002547 Transcript intron_variant - - - - - - rs4287981 4:174876684 T - - - intergenic_variant - - - - - - rs4257638 4:174894076 G - - - intergenic_variant - - - - - - rs6553759 4:174910635 C - - - intergenic_variant - - - - - - rs4321611 4:174918070 C - - - intergenic_variant - - - - - - rs6553764 4:174966594 G - - - intergenic_variant - - - - - - rs10034174 4:174968457 A - - - intergenic_variant - - - - - - rs1540447 4:174978292 T - - - intergenic_variant - - - - - - rs9992070 4:174981917 C - - - intergenic_variant - - - - - - rs2196369 4:174992464 G - - - intergenic_variant - - - - - - rs13110788 4:174992974 C - - - intergenic_variant - - - - - - rs2117808 4:174997851 T - - - intergenic_variant - - - - - - rs2196366 4:175000414 G - - - intergenic_variant - - - - - - rs2196365 4:175006356 G - - - intergenic_variant - - - - - - rs6816877 4:175015071 G - - - intergenic_variant - - - - - - rs1540458 4:175020293 C - - - intergenic_variant - - - - - - rs6553768 4:175063450 A - - - intergenic_variant - - - - - - rs1346270 4:175444055 C CCDS54821.1 CCDS54821.1 Transcript upstream_gene_variant - - - - - - DISTANCE=453 rs1346270 4:175444055 C ENSESTG00000018374 ENSESTT00000046270 Transcript intron_variant - - - - - - rs1346270 4:175444055 C 3248 NM_001256305.1 Transcript upstream_gene_variant - - - - - - DISTANCE=6 rs1346270 4:175444055 C 3248 NM_001256307.1 Transcript upstream_gene_variant - - - - - - DISTANCE=6 rs1346270 4:175444055 C 3248 NM_000860.5 Transcript upstream_gene_variant - - - - - - DISTANCE=6 rs1346270 4:175444055 C CCDS3821.1 CCDS3821.1 Transcript upstream_gene_variant - - - - - - DISTANCE=453 rs1346270 4:175444055 C CCDS58935.1 CCDS58935.1 Transcript upstream_gene_variant - - - - - - DISTANCE=453 rs1346270 4:175444055 C 3248 NM_001256306.1 Transcript upstream_gene_variant - - - - - - DISTANCE=6 rs1346270 4:175444055 C ENSESTG00000018374 ENSESTT00000046313 Transcript upstream_gene_variant - - - - - - DISTANCE=416 rs1346270 4:175444055 C 3248 NM_001256301.1 Transcript upstream_gene_variant - - - - - - DISTANCE=11 rs1346270 4:175444055 C 3248 NM_001145816.2 Transcript upstream_gene_variant - - - - - - DISTANCE=6 rs1346270 4:175444055 C CCDS58934.1 CCDS58934.1 Transcript upstream_gene_variant - - - - - - DISTANCE=453 rs2555647 4:175506300 G - - - intergenic_variant - - - - - - rs1426948 4:175519082 G - - - intergenic_variant - - - - - - rs4695944 4:175569892 G CCDS3822.1 CCDS3822.1 Transcript intron_variant - - - - - - rs4695944 4:175569892 G 8001 NM_001042543.1 Transcript intron_variant - - - - - - rs4695944 4:175569892 G CCDS43283.1 CCDS43283.1 Transcript intron_variant - - - - - - rs4695944 4:175569892 G 8001 NM_006529.2 Transcript intron_variant - - - - - - rs1032360 4:175802183 T - - - intergenic_variant - - - - - - rs10002544 4:175919466 A - - - intergenic_variant - - - - - - rs1824910 4:175965080 T - - - intergenic_variant - - - - - - rs330455 4:175992323 A - - - intergenic_variant - - - - - - rs450908 4:176100979 G - - - intergenic_variant - - - - - - rs4690660 4:176401791 G - - - intergenic_variant - - - - - - rs6553883 4:176451900 T - - - intergenic_variant - - - - - - rs13151999 4:176483328 A - - - intergenic_variant - - - - - - rs2333232 4:176535027 G - - - intergenic_variant - - - - - - rs6824420 4:176589622 G ENSESTG00000003301 ENSESTT00000008309 Transcript intron_variant - - - - - - rs6824420 4:176589622 G 2823 NM_005277.4 Transcript intron_variant - - - - - - rs6824420 4:176589622 G 2823 NR_048571.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6824420 4:176589622 G ENSESTG00000003301 ENSESTT00000008328 Transcript intron_variant - - - - - - rs6824420 4:176589622 G CCDS3824.1 CCDS3824.1 Transcript intron_variant - - - - - - rs6824420 4:176589622 G CCDS58936.1 CCDS58936.1 Transcript intron_variant - - - - - - rs6824420 4:176589622 G ENSESTG00000003301 ENSESTT00000008339 Transcript intron_variant - - - - - - rs6824420 4:176589622 G CCDS54822.1 CCDS54822.1 Transcript intron_variant - - - - - - rs6824420 4:176589622 G ENSESTG00000003301 ENSESTT00000008241 Transcript intron_variant - - - - - - rs6824420 4:176589622 G ENSESTG00000003301 ENSESTT00000008273 Transcript intron_variant - - - - - - rs6824420 4:176589622 G ENSESTG00000003301 ENSESTT00000008253 Transcript intron_variant - - - - - - rs6824420 4:176589622 G 2823 NM_201591.2 Transcript intron_variant - - - - - - rs6824420 4:176589622 G ENSESTG00000003301 ENSESTT00000008342 Transcript intron_variant - - - - - - rs6824420 4:176589622 G 2823 NM_001261447.1 Transcript intron_variant - - - - - - rs6824420 4:176589622 G 2823 NM_001261448.1 Transcript intron_variant - - - - - - rs6824420 4:176589622 G ENSESTG00000003301 ENSESTT00000008300 Transcript intron_variant - - - - - - rs6824420 4:176589622 G ENSESTG00000003301 ENSESTT00000008303 Transcript intron_variant - - - - - - rs6824420 4:176589622 G 2823 NM_201592.2 Transcript intron_variant - - - - - - rs7665951 4:176727293 G ENSESTG00000003301 ENSESTT00000008309 Transcript intron_variant - - - - - - rs7665951 4:176727293 G 2823 NM_005277.4 Transcript intron_variant - - - - - - rs7665951 4:176727293 G 2823 NR_048571.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7665951 4:176727293 G CCDS3824.1 CCDS3824.1 Transcript intron_variant - - - - - - rs7665951 4:176727293 G ENSESTG00000003301 ENSESTT00000008276 Transcript intron_variant - - - - - - rs7665951 4:176727293 G CCDS54822.1 CCDS54822.1 Transcript intron_variant - - - - - - rs7665951 4:176727293 G ENSESTG00000003301 ENSESTT00000008241 Transcript intron_variant - - - - - - rs7665951 4:176727293 G ENSESTG00000003301 ENSESTT00000008273 Transcript intron_variant - - - - - - rs7665951 4:176727293 G ENSESTG00000003301 ENSESTT00000008253 Transcript intron_variant - - - - - - rs7665951 4:176727293 G ENSESTG00000003301 ENSESTT00000008292 Transcript intron_variant - - - - - - rs7665951 4:176727293 G ENSESTG00000003301 ENSESTT00000008260 Transcript intron_variant - - - - - - rs7665951 4:176727293 G 2823 NM_201591.2 Transcript intron_variant - - - - - - rs7665951 4:176727293 G 2823 NM_001261447.1 Transcript intron_variant - - - - - - rs7665951 4:176727293 G ENSESTG00000003301 ENSESTT00000008300 Transcript intron_variant - - - - - - rs7665951 4:176727293 G ENSESTG00000003301 ENSESTT00000008303 Transcript intron_variant - - - - - - rs7665951 4:176727293 G 2823 NM_201592.2 Transcript intron_variant - - - - - - rs4690649 4:176890975 C ENSESTG00000003301 ENSESTT00000008273 Transcript intron_variant - - - - - - rs4690649 4:176890975 C ENSESTG00000003301 ENSESTT00000008241 Transcript intron_variant - - - - - - rs4690649 4:176890975 C ENSESTG00000003301 ENSESTT00000008253 Transcript intron_variant - - - - - - rs4690649 4:176890975 C 2823 NM_005277.4 Transcript intron_variant - - - - - - rs4690649 4:176890975 C 2823 NR_048571.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4690649 4:176890975 C ENSESTG00000003301 ENSESTT00000008260 Transcript intron_variant - - - - - - rs4690649 4:176890975 C 2823 NM_001261447.1 Transcript intron_variant - - - - - - rs4690649 4:176890975 C CCDS54822.1 CCDS54822.1 Transcript intron_variant - - - - - - rs4690649 4:176890975 C 2823 NM_201592.2 Transcript intron_variant - - - - - - rs4642183 4:177405102 G - - - intergenic_variant - - - - - - rs1982771 4:177611618 T ENSESTG00000017455 ENSESTT00000043953 Transcript intron_variant - - - - - - rs1982771 4:177611618 T ENSESTG00000031864 ENSESTT00000080407 Transcript intron_variant - - - - - - rs1982771 4:177611618 T CCDS43285.1 CCDS43285.1 Transcript intron_variant - - - - - - rs1982771 4:177611618 T 7424 NM_005429.2 Transcript intron_variant - - - - - - rs1116747 4:178672847 A 285501 NR_028342.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1454209 4:178781462 A ENSESTG00000031349 ENSESTT00000079094 Transcript intron_variant - - - - - - rs1454209 4:178781462 A 285501 NR_028342.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1381704 4:178860001 G 285501 NR_028342.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2702415 4:179501283 G - - - intergenic_variant - - - - - - rs2570748 4:179582549 T - - - intergenic_variant - - - - - - rs364951 4:179652396 G - - - intergenic_variant - - - - - - rs6841280 4:180579592 T - - - intergenic_variant - - - - - - rs7675678 4:181154292 C - - - intergenic_variant - - - - - - rs1447321 4:181157205 C - - - intergenic_variant - - - - - - rs1550885 4:181158180 T - - - intergenic_variant - - - - - - rs9996840 4:181158565 T - - - intergenic_variant - - - - - - rs2309255 4:181198628 T - - - intergenic_variant - - - - - - rs4408995 4:181357472 C - - - intergenic_variant - - - - - - rs6831216 4:181400135 C - - - intergenic_variant - - - - - - rs3095974 4:181464034 A - ENSR00001255102 RegulatoryFeature regulatory_region_variant - - - - - - rs3095974 4:181464034 A - - - intergenic_variant - - - - - - rs3095969 4:181484716 G - - - intergenic_variant - - - - - - rs2926687 4:181732821 A - ENSR00001255131 RegulatoryFeature regulatory_region_variant - - - - - - rs2926687 4:181732821 A - - - intergenic_variant - - - - - - rs1879910 4:181803184 T - - - intergenic_variant - - - - - - rs1454708 4:182125361 G - ENSR00001437859 RegulatoryFeature regulatory_region_variant - - - - - - rs1454708 4:182125361 G ENSESTG00000016560 ENSESTT00000041516 Transcript intron_variant - - - - - - rs6836629 4:182130019 T ENSESTG00000016560 ENSESTT00000041516 Transcript intron_variant - - - - - - rs1584938 4:182134736 G ENSESTG00000016560 ENSESTT00000041516 Transcript upstream_gene_variant - - - - - - DISTANCE=4633 rs1902109 4:182149141 A - - - intergenic_variant - - - - - - rs4418018 4:182732046 G - - - intergenic_variant - - - - - - rs1040198 4:182791549 A - ENSR00001255213 RegulatoryFeature regulatory_region_variant - - - - - - rs1040198 4:182791549 A ENSESTG00000010981 ENSESTT00000027542 Transcript downstream_gene_variant - - - - - - DISTANCE=4042 rs2675524 4:183249782 C CCDS47165.1 CCDS47165.1 Transcript intron_variant - - - - - - rs2675524 4:183249782 C ENSESTG00000006974 ENSESTT00000017667 Transcript intron_variant - - - - - - rs2675524 4:183249782 C 55714 NM_001080477.1 Transcript intron_variant - - - - - - rs2675524 4:183249782 C ENSESTG00000010967 ENSESTT00000027464 Transcript intron_variant - - - - - - rs10866256 4:183652175 C - ENSR00001255333 RegulatoryFeature regulatory_region_variant - - - - - - rs10866256 4:183652175 C ENSESTG00000006985 ENSESTT00000017702 Transcript downstream_gene_variant - - - - - - DISTANCE=1943 rs10866256 4:183652175 C CCDS47165.1 CCDS47165.1 Transcript synonymous_variant 2850 2850 950 D gaT/gaC - rs10866256 4:183652175 C 55714 NM_001080477.1 Transcript synonymous_variant 2887 2850 950 D gaT/gaC - rs10866256 4:183652175 C ENSESTG00000006990 ENSESTT00000017710 Transcript synonymous_variant 333 147 49 D gaT/gaC - rs10866256 4:183652175 C ENSESTG00000006985 ENSESTT00000017701 Transcript downstream_gene_variant - - - - - - DISTANCE=1943 rs13145965 4:183785918 C - - - intergenic_variant - - - - - - rs2714502 4:183965515 C 403315 NR_003612.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4243 rs1355497 4:184148050 A CCDS34109.2 CCDS34109.2 Transcript intron_variant - - - - - - rs1355497 4:184148050 A 80014 NM_024949.5 Transcript intron_variant - - - - - - rs1355497 4:184148050 A ENSESTG00000007009 ENSESTT00000017792 Transcript intron_variant - - - - - - rs1355497 4:184148050 A ENSESTG00000007009 ENSESTT00000017802 Transcript intron_variant - - - - - - rs1355497 4:184148050 A ENSESTG00000007009 ENSESTT00000017799 Transcript intron_variant - - - - - - rs1355497 4:184148050 A ENSESTG00000007009 ENSESTT00000017796 Transcript intron_variant - - - - - - rs2309952 4:184904718 G ENSESTG00000019436 ENSESTT00000048813 Transcript upstream_gene_variant - - - - - - DISTANCE=4113 rs2309952 4:184904718 G ENSESTG00000019395 ENSESTT00000048794 Transcript intron_variant - - - - - - rs2309952 4:184904718 G CCDS47167.1 CCDS47167.1 Transcript intron_variant - - - - - - rs2309952 4:184904718 G ENSESTG00000019395 ENSESTT00000048717 Transcript intron_variant - - - - - - rs2309952 4:184904718 G 56977 NM_020225.1 Transcript intron_variant - - - - - - rs2309952 4:184904718 G ENSESTG00000019395 ENSESTT00000048769 Transcript intron_variant - - - - - - rs6835097 4:185521864 T - - - intergenic_variant - - - - - - rs2696053 4:185585413 C CCDS3837.1 CCDS3837.1 Transcript intron_variant - - - - - - rs2696053 4:185585413 C ENSESTG00000015878 ENSESTT00000039872 Transcript intron_variant - - - - - - rs2696053 4:185585413 C 201973 NM_152683.2 Transcript intron_variant - - - - - - rs2705879 4:185585756 T - ENSR00001255740 RegulatoryFeature regulatory_region_variant - - - - - - rs2705879 4:185585756 T CCDS3837.1 CCDS3837.1 Transcript intron_variant - - - - - - rs2705879 4:185585756 T ENSESTG00000015878 ENSESTT00000039872 Transcript intron_variant - - - - - - rs2705879 4:185585756 T 201973 NM_152683.2 Transcript intron_variant - - - - - - rs4862405 4:185622433 C CCDS3838.1 CCDS3838.1 Transcript intron_variant - - - - - - rs4862405 4:185622433 C 79682 NM_024629.3 Transcript intron_variant - - - - - - rs4862405 4:185622433 C ENSESTG00000016040 ENSESTT00000040285 Transcript intron_variant - - - - - - rs4862405 4:185622433 C ENSESTG00000016040 ENSESTT00000040308 Transcript intron_variant - - - - - - rs4862405 4:185622433 C ENSESTG00000016040 ENSESTT00000040294 Transcript intron_variant - - - - - - rs4241794 4:185622779 G CCDS3838.1 CCDS3838.1 Transcript intron_variant - - - - - - rs4241794 4:185622779 G 79682 NM_024629.3 Transcript intron_variant - - - - - - rs4241794 4:185622779 G ENSESTG00000016040 ENSESTT00000040285 Transcript intron_variant - - - - - - rs4241794 4:185622779 G ENSESTG00000016040 ENSESTT00000040308 Transcript intron_variant - - - - - - rs4241794 4:185622779 G ENSESTG00000016040 ENSESTT00000040294 Transcript intron_variant - - - - - - rs7659922 4:185649530 G CCDS3838.1 CCDS3838.1 Transcript intron_variant - - - - - - rs7659922 4:185649530 G 79682 NM_024629.3 Transcript intron_variant - - - - - - rs7659922 4:185649530 G ENSESTG00000016040 ENSESTT00000040285 Transcript intron_variant - - - - - - rs7659922 4:185649530 G ENSESTG00000016040 ENSESTT00000040294 Transcript intron_variant - - - - - - rs6843169 4:185649852 C CCDS3838.1 CCDS3838.1 Transcript intron_variant - - - - - - rs6843169 4:185649852 C 79682 NM_024629.3 Transcript intron_variant - - - - - - rs6843169 4:185649852 C ENSESTG00000016040 ENSESTT00000040285 Transcript intron_variant - - - - - - rs6843169 4:185649852 C ENSESTG00000016040 ENSESTT00000040294 Transcript intron_variant - - - - - - rs6845141 4:185653924 G CCDS3838.1 CCDS3838.1 Transcript intron_variant - - - - - - rs6845141 4:185653924 G 79682 NM_024629.3 Transcript intron_variant - - - - - - rs6845141 4:185653924 G ENSESTG00000016040 ENSESTT00000040285 Transcript intron_variant - - - - - - rs6845141 4:185653924 G ENSESTG00000016040 ENSESTT00000040294 Transcript intron_variant - - - - - - rs902175 4:185654676 C - ENSR00001255750 RegulatoryFeature regulatory_region_variant - - - - - - rs902175 4:185654676 C CCDS3838.1 CCDS3838.1 Transcript intron_variant - - - - - - rs902175 4:185654676 C 79682 NM_024629.3 Transcript intron_variant - - - - - - rs902175 4:185654676 C ENSESTG00000016040 ENSESTT00000040285 Transcript intron_variant - - - - - - rs902175 4:185654676 C ENSESTG00000016040 ENSESTT00000040294 Transcript intron_variant - - - - - - rs7675463 4:185669576 G - ENSR00001438113 RegulatoryFeature regulatory_region_variant - - - - - - rs7675463 4:185669576 G - - - intergenic_variant - - - - - - rs4862413 4:185678118 G CCDS3839.1 CCDS3839.1 Transcript downstream_gene_variant - - - - - - DISTANCE=161 rs4862413 4:185678118 G 2180 NM_001995.2 Transcript 3_prime_UTR_variant 2436 - - - - - rs939040 4:185683840 G CCDS3839.1 CCDS3839.1 Transcript intron_variant - - - - - - rs939040 4:185683840 G 2180 NM_001995.2 Transcript intron_variant - - - - - - rs4862414 4:185688651 A ENSESTG00000015979 ENSESTT00000040157 Transcript downstream_gene_variant - - - - - - DISTANCE=2908 rs4862414 4:185688651 A ENSESTG00000015979 ENSESTT00000040139 Transcript downstream_gene_variant - - - - - - DISTANCE=2908 rs4862414 4:185688651 A ENSESTG00000015979 ENSESTT00000040114 Transcript downstream_gene_variant - - - - - - DISTANCE=2908 rs4862414 4:185688651 A ENSESTG00000015979 ENSESTT00000040119 Transcript downstream_gene_variant - - - - - - DISTANCE=2908 rs4862414 4:185688651 A ENSESTG00000015979 ENSESTT00000040203 Transcript downstream_gene_variant - - - - - - DISTANCE=2908 rs4862414 4:185688651 A ENSESTG00000015979 ENSESTT00000040132 Transcript downstream_gene_variant - - - - - - DISTANCE=2908 rs4862414 4:185688651 A ENSESTG00000015979 ENSESTT00000040184 Transcript downstream_gene_variant - - - - - - DISTANCE=2908 rs4862414 4:185688651 A 2180 NM_001995.2 Transcript intron_variant - - - - - - rs4862414 4:185688651 A CCDS3839.1 CCDS3839.1 Transcript intron_variant - - - - - - rs4862414 4:185688651 A ENSESTG00000015979 ENSESTT00000040106 Transcript downstream_gene_variant - - - - - - DISTANCE=2908 rs12508858 4:185696248 A ENSESTG00000015979 ENSESTT00000040157 Transcript intron_variant - - - - - - rs12508858 4:185696248 A ENSESTG00000015979 ENSESTT00000040139 Transcript intron_variant - - - - - - rs12508858 4:185696248 A ENSESTG00000015979 ENSESTT00000040114 Transcript intron_variant - - - - - - rs12508858 4:185696248 A ENSESTG00000015979 ENSESTT00000040119 Transcript intron_variant - - - - - - rs12508858 4:185696248 A ENSESTG00000015979 ENSESTT00000040203 Transcript intron_variant - - - - - - rs12508858 4:185696248 A ENSESTG00000015979 ENSESTT00000040132 Transcript intron_variant - - - - - - rs12508858 4:185696248 A ENSESTG00000015979 ENSESTT00000040184 Transcript intron_variant - - - - - - rs12508858 4:185696248 A 2180 NM_001995.2 Transcript intron_variant - - - - - - rs12508858 4:185696248 A CCDS3839.1 CCDS3839.1 Transcript intron_variant - - - - - - rs12508858 4:185696248 A ENSESTG00000015979 ENSESTT00000040106 Transcript intron_variant - - - - - - rs1873226 4:185697441 T ENSESTG00000015979 ENSESTT00000040157 Transcript intron_variant - - - - - - rs1873226 4:185697441 T ENSESTG00000015979 ENSESTT00000040139 Transcript intron_variant - - - - - - rs1873226 4:185697441 T ENSESTG00000015979 ENSESTT00000040114 Transcript intron_variant - - - - - - rs1873226 4:185697441 T ENSESTG00000015979 ENSESTT00000040119 Transcript intron_variant - - - - - - rs1873226 4:185697441 T ENSESTG00000015979 ENSESTT00000040203 Transcript intron_variant - - - - - - rs1873226 4:185697441 T ENSESTG00000015979 ENSESTT00000040132 Transcript intron_variant - - - - - - rs1873226 4:185697441 T ENSESTG00000015979 ENSESTT00000040184 Transcript intron_variant - - - - - - rs1873226 4:185697441 T 2180 NM_001995.2 Transcript intron_variant - - - - - - rs1873226 4:185697441 T CCDS3839.1 CCDS3839.1 Transcript intron_variant - - - - - - rs1873226 4:185697441 T ENSESTG00000015979 ENSESTT00000040106 Transcript intron_variant - - - - - - rs1968957 4:185704590 C ENSESTG00000015979 ENSESTT00000040157 Transcript intron_variant - - - - - - rs1968957 4:185704590 C ENSESTG00000015979 ENSESTT00000040139 Transcript intron_variant - - - - - - rs1968957 4:185704590 C ENSESTG00000015979 ENSESTT00000040114 Transcript intron_variant - - - - - - rs1968957 4:185704590 C ENSESTG00000015979 ENSESTT00000040119 Transcript intron_variant - - - - - - rs1968957 4:185704590 C ENSESTG00000015979 ENSESTT00000040203 Transcript intron_variant - - - - - - rs1968957 4:185704590 C ENSESTG00000015979 ENSESTT00000040132 Transcript intron_variant - - - - - - rs1968957 4:185704590 C ENSESTG00000015979 ENSESTT00000040184 Transcript intron_variant - - - - - - rs1968957 4:185704590 C 2180 NM_001995.2 Transcript intron_variant - - - - - - rs1968957 4:185704590 C CCDS3839.1 CCDS3839.1 Transcript intron_variant - - - - - - rs1968957 4:185704590 C ENSESTG00000015979 ENSESTT00000040106 Transcript intron_variant - - - - - - rs7683824 4:185972317 G - - - intergenic_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005349 Transcript intron_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005321 Transcript intron_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005284 Transcript intron_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005351 Transcript intron_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005325 Transcript intron_variant - - - - - - rs7665083 4:186837063 G 8470 NM_021069.4 Transcript intron_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005303 Transcript intron_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005336 Transcript intron_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005339 Transcript intron_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005273 Transcript intron_variant - - - - - - rs7665083 4:186837063 G ENSESTG00000002132 ENSESTT00000005317 Transcript intron_variant - - - - - - rs1867068 4:187446705 G ENSESTG00000018497 ENSESTT00000046573 Transcript intron_variant - - - - - - rs4862722 4:187530313 T ENSESTG00000018359 ENSESTT00000046333 Transcript intron_variant - - - - - - rs4862722 4:187530313 T 2195 NM_005245.3 Transcript intron_variant - - - - - - rs4862722 4:187530313 T CCDS47177.1 CCDS47177.1 Transcript intron_variant - - - - - - rs4862722 4:187530313 T ENSESTG00000018359 ENSESTT00000046339 Transcript intron_variant - - - - - - rs327112 4:187605689 A 2195 NM_005245.3 Transcript intron_variant - - - - - - rs327112 4:187605689 A CCDS47177.1 CCDS47177.1 Transcript intron_variant - - - - - - rs13119331 4:187878435 C - - - intergenic_variant - - - - - - rs4441812 4:188853588 A - - - intergenic_variant - - - - - - rs4861766 4:189017038 T 205860 NM_173553.1 Transcript intron_variant - - - - - - rs4861766 4:189017038 T CCDS3850.1 CCDS3850.1 Transcript intron_variant - - - - - - rs821977 5:95578 G ENSESTG00000033107 ENSESTT00000083666 Transcript intron_variant - - - - - - rs239344 5:367776 C ENSESTG00000020887 ENSESTT00000052376 Transcript intron_variant - - - - - - rs239344 5:367776 C CCDS56355.1 CCDS56355.1 Transcript intron_variant - - - - - - rs239344 5:367776 C ENSESTG00000020887 ENSESTT00000052430 Transcript intron_variant - - - - - - rs239344 5:367776 C 57491 NM_020731.4 Transcript intron_variant - - - - - - rs239344 5:367776 C CCDS43297.1 CCDS43297.1 Transcript intron_variant - - - - - - rs239344 5:367776 C ENSESTG00000020887 ENSESTT00000052395 Transcript intron_variant - - - - - - rs239344 5:367776 C ENSESTG00000020887 ENSESTT00000052416 Transcript intron_variant - - - - - - rs239344 5:367776 C 57491 NM_001242412.1 Transcript intron_variant - - - - - - rs349575 5:370868 G ENSESTG00000020887 ENSESTT00000052376 Transcript intron_variant - - - - - - rs349575 5:370868 G CCDS56355.1 CCDS56355.1 Transcript intron_variant - - - - - - rs349575 5:370868 G ENSESTG00000020887 ENSESTT00000052430 Transcript downstream_gene_variant - - - - - - DISTANCE=2653 rs349575 5:370868 G 57491 NM_020731.4 Transcript intron_variant - - - - - - rs349575 5:370868 G CCDS43297.1 CCDS43297.1 Transcript intron_variant - - - - - - rs349575 5:370868 G ENSESTG00000020887 ENSESTT00000052395 Transcript intron_variant - - - - - - rs349575 5:370868 G ENSESTG00000020887 ENSESTT00000052416 Transcript downstream_gene_variant - - - - - - DISTANCE=2644 rs349575 5:370868 G 57491 NM_001242412.1 Transcript intron_variant - - - - - - rs2721030 5:483002 G - ENSR00001274020 RegulatoryFeature regulatory_region_variant - - - - - - rs2721030 5:483002 G 6550 NM_004174.2 Transcript intron_variant - - - - - - rs2721030 5:483002 G ENSESTG00000021218 ENSESTT00000053304 Transcript downstream_gene_variant - - - - - - DISTANCE=2797 rs2721030 5:483002 G ENSESTG00000021218 ENSESTT00000053284 Transcript downstream_gene_variant - - - - - - DISTANCE=4974 rs2721030 5:483002 G ENSESTG00000022809 ENSESTT00000057504 Transcript upstream_gene_variant - - - - - - DISTANCE=241 rs2721030 5:483002 G ENSESTG00000022789 ENSESTT00000057462 Transcript downstream_gene_variant - - - - - - DISTANCE=368 rs2721030 5:483002 G ENSESTG00000021218 ENSESTT00000053338 Transcript downstream_gene_variant - - - - - - DISTANCE=2676 rs2721030 5:483002 G CCDS3855.1 CCDS3855.1 Transcript intron_variant - - - - - - rs2721030 5:483002 G ENSESTG00000021218 ENSESTT00000053316 Transcript downstream_gene_variant - - - - - - DISTANCE=2736 rs2166298 5:946041 C - ENSR00001274217 RegulatoryFeature regulatory_region_variant - - - - - - rs2166298 5:946041 C ENSESTG00000021699 ENSESTT00000054475 Transcript upstream_gene_variant - - - - - - DISTANCE=389 rs4246735 5:1029737 C CCDS3859.1 CCDS3859.1 Transcript intron_variant - - - - - - rs4246735 5:1029737 C 85409 NM_033120.2 Transcript intron_variant - - - - - - rs4246735 5:1029737 C ENSESTG00000002638 ENSESTT00000006566 Transcript intron_variant - - - - - - rs4276451 5:1108945 G ENSESTG00000002852 ENSESTT00000007091 Transcript intron_variant - - - - - - rs4276451 5:1108945 G ENSESTG00000002651 ENSESTT00000006581 Transcript upstream_gene_variant - - - - - - DISTANCE=1949 rs4276451 5:1108945 G ENSESTG00000002852 ENSESTT00000007095 Transcript intron_variant - - - - - - rs4276451 5:1108945 G CCDS34129.1 CCDS34129.1 Transcript intron_variant - - - - - - rs4276451 5:1108945 G 10723 NM_006598.2 Transcript intron_variant - - - - - - rs37016 5:1380153 C ENSESTG00000002797 ENSESTT00000006938 Transcript 5_prime_UTR_variant 2 - - - - - rs37016 5:1380153 C ENSESTG00000002797 ENSESTT00000006934 Transcript 5_prime_UTR_variant 11 - - - - - rs6420034 5:2051869 C - - - intergenic_variant - - - - - - rs462938 5:2354979 A - - - intergenic_variant - - - - - - rs315898 5:2427740 G - - - intergenic_variant - - - - - - rs3099583 5:2493094 C - - - intergenic_variant - - - - - - rs323679 5:2652908 G - - - intergenic_variant - - - - - - rs2962596 5:2705659 G - - - intergenic_variant - - - - - - rs2935611 5:2733921 G - - - intergenic_variant - - - - - - rs1497458 5:2800016 T - - - intergenic_variant - - - - - - rs160762 5:3114890 T - - - intergenic_variant - - - - - - rs2934816 5:3170008 A - - - intergenic_variant - - - - - - rs4866551 5:3308401 C - ENSR00001274655 RegulatoryFeature regulatory_region_variant - - - - - - rs4866551 5:3308401 C - - - intergenic_variant - - - - - - rs828321 5:3547194 T - - - intergenic_variant - - - - - - rs828305 5:3576371 G - - - intergenic_variant - - - - - - rs10038168 5:3652798 A - - - intergenic_variant - - - - - - rs6872227 5:3684040 G - - - intergenic_variant - - - - - - rs6872377 5:3684085 G - - - intergenic_variant - - - - - - rs2967830 5:3871405 A - - - intergenic_variant - - - - - - rs622565 5:3905946 C - - - intergenic_variant - - - - - - rs670531 5:3927539 T - - - intergenic_variant - - - - - - rs621068 5:3951441 C - - - intergenic_variant - - - - - - rs10055081 5:4185322 C - - - intergenic_variant - - - - - - rs7380589 5:4404351 C - - - intergenic_variant - - - - - - rs6555297 5:4529652 G - - - intergenic_variant - - - - - - rs1875495 5:4731638 G - - - intergenic_variant - - - - - - rs1532689 5:4782284 C ENSESTG00000017449 ENSESTT00000043875 Transcript intron_variant - - - - - - rs816453 5:4848338 G ENSESTG00000017444 ENSESTT00000043869 Transcript intron_variant - - - - - - rs270645 5:5070347 T ENSESTG00000025008 ENSESTT00000063125 Transcript downstream_gene_variant - - - - - - DISTANCE=2882 rs270645 5:5070347 T ENSESTG00000025226 ENSESTT00000063645 Transcript intron_variant - - - - - - rs270645 5:5070347 T 340094 NR_026994.1 Transcript downstream_gene_variant - - - - - - DISTANCE=230 rs1382897 5:5089096 G - - - intergenic_variant - - - - - - rs814793 5:5100552 A - - - intergenic_variant - - - - - - rs1092984 5:5117789 T - - - intergenic_variant - - - - - - rs270177 5:5167000 A 170690 NM_139056.2 Transcript intron_variant - - - - - - rs270177 5:5167000 A ENSESTG00000025196 ENSESTT00000063552 Transcript intron_variant - - - - - - rs270177 5:5167000 A ENSESTG00000025037 ENSESTT00000063205 Transcript intron_variant - - - - - - rs270177 5:5167000 A CCDS43299.1 CCDS43299.1 Transcript intron_variant - - - - - - rs270177 5:5167000 A ENSESTG00000025203 ENSESTT00000063584 Transcript intron_variant - - - - - - rs7732927 5:5310062 G 170690 NM_139056.2 Transcript intron_variant - - - - - - rs7732927 5:5310062 G ENSESTG00000025155 ENSESTT00000063478 Transcript intron_variant - - - - - - rs7732927 5:5310062 G CCDS43299.1 CCDS43299.1 Transcript intron_variant - - - - - - rs7732927 5:5310062 G ENSESTG00000025083 ENSESTT00000063306 Transcript intron_variant - - - - - - rs2964143 5:5362785 C ENSESTG00000025155 ENSESTT00000063478 Transcript intron_variant - - - - - - rs1501989 5:5619585 C - - - intergenic_variant - - - - - - rs256483 5:5690795 T - - - intergenic_variant - - - - - - rs2617532 5:5773518 A - - - intergenic_variant - - - - - - rs460906 5:6026378 A - - - intergenic_variant - - - - - - rs154815 5:6029164 C - - - intergenic_variant - - - - - - rs2638607 5:6079280 C - - - intergenic_variant - - - - - - rs823670 5:6081585 C - - - intergenic_variant - - - - - - rs2964711 5:6281578 C - - - intergenic_variant - - - - - - rs2914750 5:6285652 C - - - intergenic_variant - - - - - - rs275451 5:6816909 C ENSESTG00000016185 ENSESTT00000040593 Transcript intron_variant - - - - - - rs6874514 5:7149753 T ENSESTG00000016190 ENSESTT00000040607 Transcript intron_variant - - - - - - rs4357002 5:7247078 G - - - intergenic_variant - - - - - - rs11950018 5:7492554 C ENSESTG00000017800 ENSESTT00000045102 Transcript intron_variant - - - - - - rs11950018 5:7492554 C 108 NM_020546.2 Transcript intron_variant - - - - - - rs11950018 5:7492554 C CCDS3872.2 CCDS3872.2 Transcript intron_variant - - - - - - rs11950018 5:7492554 C ENSESTG00000017800 ENSESTT00000045116 Transcript intron_variant - - - - - - rs9313200 5:7616238 A ENSESTG00000017800 ENSESTT00000045129 Transcript intron_variant - - - - - - rs9313200 5:7616238 A ENSESTG00000017800 ENSESTT00000045102 Transcript intron_variant - - - - - - rs9313200 5:7616238 A 108 NM_020546.2 Transcript intron_variant - - - - - - rs9313200 5:7616238 A ENSESTG00000017800 ENSESTT00000045139 Transcript intron_variant - - - - - - rs9313200 5:7616238 A CCDS3872.2 CCDS3872.2 Transcript intron_variant - - - - - - rs9313200 5:7616238 A ENSESTG00000017800 ENSESTT00000045116 Transcript intron_variant - - - - - - rs7448733 5:8541979 G - - - intergenic_variant - - - - - - rs3111122 5:8802367 G - - - intergenic_variant - - - - - - rs2962680 5:8904851 G - - - intergenic_variant - - - - - - rs40668 5:9223274 A ENSESTG00000017338 ENSESTT00000043605 Transcript downstream_gene_variant - - - - - - DISTANCE=1671 rs40668 5:9223274 A CCDS3875.1 CCDS3875.1 Transcript intron_variant - - - - - - rs40668 5:9223274 A ENSESTG00000017338 ENSESTT00000043710 Transcript intron_variant - - - - - - rs40668 5:9223274 A 9037 NM_003966.2 Transcript intron_variant - - - - - - rs42349 5:9242554 T ENSESTG00000017338 ENSESTT00000043605 Transcript intron_variant - - - - - - rs42349 5:9242554 T CCDS3875.1 CCDS3875.1 Transcript intron_variant - - - - - - rs42349 5:9242554 T ENSESTG00000017338 ENSESTT00000043710 Transcript upstream_gene_variant - - - - - - DISTANCE=4550 rs42349 5:9242554 T 9037 NM_003966.2 Transcript intron_variant - - - - - - rs7715373 5:9271150 G ENSESTG00000017338 ENSESTT00000043605 Transcript intron_variant - - - - - - rs7715373 5:9271150 G CCDS3875.1 CCDS3875.1 Transcript intron_variant - - - - - - rs7715373 5:9271150 G 9037 NM_003966.2 Transcript intron_variant - - - - - - rs6555597 5:9280957 A ENSESTG00000017338 ENSESTT00000043605 Transcript intron_variant - - - - - - rs6555597 5:9280957 A CCDS3875.1 CCDS3875.1 Transcript intron_variant - - - - - - rs6555597 5:9280957 A 9037 NM_003966.2 Transcript intron_variant - - - - - - rs268506 5:9464999 C ENSESTG00000017306 ENSESTT00000043549 Transcript intron_variant - - - - - - rs268506 5:9464999 C 9037 NM_003966.2 Transcript intron_variant - - - - - - rs435780 5:9490319 G ENSESTG00000017306 ENSESTT00000043549 Transcript intron_variant - - - - - - rs435780 5:9490319 G 9037 NM_003966.2 Transcript intron_variant - - - - - - rs150623 5:9571863 C - - - intergenic_variant - - - - - - rs2963863 5:9851189 G 285692 NR_027112.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs2963863 5:9851189 G ENSESTG00000017278 ENSESTT00000043389 Transcript upstream_gene_variant - - - - - - DISTANCE=3300 rs2905189 5:9878708 T 285692 NR_027112.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs2905189 5:9878708 T ENSESTG00000017278 ENSESTT00000043389 Transcript intron_variant - - - - - - rs12655719 5:9893398 C 285692 NR_027112.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs12655719 5:9893398 C ENSESTG00000017278 ENSESTT00000043389 Transcript downstream_gene_variant - - - - - - DISTANCE=3349 rs4432857 5:9912275 G - - - intergenic_variant - - - - - - rs2963886 5:9926136 T - - - intergenic_variant - - - - - - rs2963882 5:9932431 G - - - intergenic_variant - - - - - - rs6864706 5:10106321 G - - - intergenic_variant - - - - - - rs2607304 5:10246741 G CCDS58942.1 CCDS58942.1 Transcript intron_variant - - - - - - rs2607304 5:10246741 G 134145 NM_001258389.1 Transcript intron_variant - - - - - - rs2607304 5:10246741 G 134145 NM_001258388.1 Transcript intron_variant - - - - - - rs2607304 5:10246741 G 134145 NM_199133.3 Transcript intron_variant - - - - - - rs2607304 5:10246741 G ENSESTG00000016690 ENSESTT00000042019 Transcript upstream_gene_variant - - - - - - DISTANCE=3669 rs2607304 5:10246741 G 134145 NR_047669.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2607304 5:10246741 G 134145 NR_047670.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2607304 5:10246741 G CCDS43301.1 CCDS43301.1 Transcript intron_variant - - - - - - rs2607304 5:10246741 G 134145 NR_047668.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2607304 5:10246741 G 22948 NM_012073.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3541 rs2607304 5:10246741 G CCDS3877.1 CCDS3877.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3712 rs2399966 5:10772371 C - - - intergenic_variant - - - - - - rs26041 5:11215836 C 1501 NM_001332.2 Transcript intron_variant - - - - - - rs26041 5:11215836 C CCDS3881.1 CCDS3881.1 Transcript intron_variant - - - - - - rs26041 5:11215836 C ENSESTG00000009051 ENSESTT00000022847 Transcript intron_variant - - - - - - rs32259 5:11222735 T 1501 NM_001332.2 Transcript intron_variant - - - - - - rs32259 5:11222735 T CCDS3881.1 CCDS3881.1 Transcript intron_variant - - - - - - rs32259 5:11222735 T ENSESTG00000009051 ENSESTT00000022847 Transcript intron_variant - - - - - - rs31750 5:11412302 T 1501 NM_001332.2 Transcript intron_variant - - - - - - rs31750 5:11412302 T CCDS3881.1 CCDS3881.1 Transcript intron_variant - - - - - - rs31750 5:11412302 T ENSESTG00000009051 ENSESTT00000022849 Transcript intron_variant - - - - - - rs31750 5:11412302 T ENSESTG00000009051 ENSESTT00000022847 Transcript intron_variant - - - - - - rs31750 5:11412302 T ENSESTG00000009051 ENSESTT00000022739 Transcript intron_variant - - - - - - rs31750 5:11412302 T ENSESTG00000009051 ENSESTT00000022752 Transcript intron_variant - - - - - - rs2561620 5:11659141 C 1501 NM_001332.2 Transcript intron_variant - - - - - - rs2561620 5:11659141 C CCDS3881.1 CCDS3881.1 Transcript intron_variant - - - - - - rs2561620 5:11659141 C ENSESTG00000009051 ENSESTT00000022744 Transcript intron_variant - - - - - - rs2561620 5:11659141 C ENSESTG00000009051 ENSESTT00000022739 Transcript intron_variant - - - - - - rs2561620 5:11659141 C ENSESTG00000009051 ENSESTT00000022752 Transcript intron_variant - - - - - - rs1119368 5:11940068 A - - - intergenic_variant - - - - - - rs6891986 5:12265518 C - - - intergenic_variant - - - - - - rs10213705 5:12291053 G - - - intergenic_variant - - - - - - rs6554694 5:12344408 T - - - intergenic_variant - - - - - - rs6554696 5:12354216 T - - - intergenic_variant - - - - - - rs6554705 5:12417025 A - - - intergenic_variant - - - - - - rs6898501 5:12511971 T - - - intergenic_variant - - - - - - rs35294527 5:12929481 A ENSESTG00000013465 ENSESTT00000033714 Transcript intron_variant - - - - - - rs4270688 5:12963288 T ENSESTG00000013465 ENSESTT00000033714 Transcript intron_variant - - - - - - rs1438280 5:12968850 T ENSESTG00000013465 ENSESTT00000033714 Transcript intron_variant - - - - - - rs1466016 5:13353554 A - - - intergenic_variant - - - - - - rs233380 5:13581019 T - - - intergenic_variant - - - - - - rs6554803 5:13699405 G CCDS3882.1 CCDS3882.1 Transcript intron_variant - - - - - - rs6554803 5:13699405 G 1767 NM_001369.2 Transcript intron_variant - - - - - - rs181591 5:14426166 T CCDS3883.1 CCDS3883.1 Transcript intron_variant - - - - - - rs181591 5:14426166 T ENSESTG00000017121 ENSESTT00000043397 Transcript intron_variant - - - - - - rs181591 5:14426166 T 7204 NM_007118.2 Transcript intron_variant - - - - - - rs181591 5:14426166 T ENSESTG00000017121 ENSESTT00000043384 Transcript intron_variant - - - - - - rs2455400 5:14641907 C - - - intergenic_variant - - - - - - rs31927 5:14677614 T ENSESTG00000017801 ENSESTT00000044877 Transcript downstream_gene_variant - - - - - - DISTANCE=3611 rs31927 5:14677614 T CCDS43302.1 CCDS43302.1 Transcript intron_variant - - - - - - rs31927 5:14677614 T ENSESTG00000017801 ENSESTT00000044910 Transcript upstream_gene_variant - - - - - - DISTANCE=4089 rs31927 5:14677614 T ENSESTG00000017801 ENSESTT00000044863 Transcript intron_variant - - - - - - rs31927 5:14677614 T 90268 NM_138348.4 Transcript intron_variant - - - - - - rs31927 5:14677614 T ENSESTG00000017801 ENSESTT00000044895 Transcript upstream_gene_variant - - - - - - DISTANCE=4005 rs31877 5:15258774 C ENSESTG00000014598 ENSESTT00000036514 Transcript intron_variant - - - - - - rs2607525 5:15291781 A - - - intergenic_variant - - - - - - rs3849084 5:15385105 T - - - intergenic_variant - - - - - - rs10058239 5:15687817 G 23194 NM_012304.3 Transcript intron_variant - - - - - - rs10058239 5:15687817 G CCDS54833.1 CCDS54833.1 Transcript intron_variant - - - - - - rs1505030 5:15868989 G 23194 NM_012304.3 Transcript intron_variant - - - - - - rs1505030 5:15868989 G CCDS54833.1 CCDS54833.1 Transcript intron_variant - - - - - - rs2263396 5:16013083 T ENSESTG00000014561 ENSESTT00000036425 Transcript intron_variant - - - - - - rs26744 5:16668167 A ENSESTG00000005233 ENSESTT00000013387 Transcript downstream_gene_variant - - - - - - DISTANCE=2544 rs26744 5:16668167 A ENSESTG00000005233 ENSESTT00000013305 Transcript downstream_gene_variant - - - - - - DISTANCE=2680 rs26744 5:16668167 A 4651 NM_012334.2 Transcript intron_variant - - - - - - rs26744 5:16668167 A CCDS54834.1 CCDS54834.1 Transcript intron_variant - - - - - - rs26744 5:16668167 A ENSESTG00000005218 ENSESTT00000013259 Transcript upstream_gene_variant - - - - - - DISTANCE=4630 rs26744 5:16668167 A ENSESTG00000005233 ENSESTT00000013353 Transcript downstream_gene_variant - - - - - - DISTANCE=2544 rs26744 5:16668167 A ENSESTG00000005233 ENSESTT00000013301 Transcript downstream_gene_variant - - - - - - DISTANCE=2680 rs26744 5:16668167 A ENSESTG00000005233 ENSESTT00000013307 Transcript downstream_gene_variant - - - - - - DISTANCE=2680 rs249124 5:16917883 C 4651 NM_012334.2 Transcript intron_variant - - - - - - rs249124 5:16917883 C ENSESTG00000005267 ENSESTT00000013413 Transcript intron_variant - - - - - - rs249124 5:16917883 C ENSESTG00000005267 ENSESTT00000013441 Transcript intron_variant - - - - - - rs249124 5:16917883 C ENSESTG00000005267 ENSESTT00000013444 Transcript upstream_gene_variant - - - - - - DISTANCE=1247 rs249124 5:16917883 C CCDS54834.1 CCDS54834.1 Transcript intron_variant - - - - - - rs1084602 5:17950770 A - - - intergenic_variant - - - - - - rs6885045 5:18679314 T - - - intergenic_variant - - - - - - rs2962216 5:18753520 G - - - intergenic_variant - - - - - - rs4410639 5:19006673 C - - - intergenic_variant - - - - - - rs7707832 5:19019264 T - ENSR00001276511 RegulatoryFeature regulatory_region_variant - - - - - - rs7707832 5:19019264 T - - - intergenic_variant - - - - - - rs10051068 5:19061127 C - - - intergenic_variant - - - - - - rs4438880 5:19157050 T - - - intergenic_variant - - - - - - rs2972818 5:19481171 C CCDS54835.1 CCDS54835.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2287 rs2972818 5:19481171 C ENSESTG00000029018 ENSESTT00000073149 Transcript upstream_gene_variant - - - - - - DISTANCE=2426 rs2972818 5:19481171 C 1016 NM_001167667.1 Transcript intron_variant - - - - - - rs2972818 5:19481171 C ENSESTG00000029018 ENSESTT00000073129 Transcript intron_variant - - - - - - rs2972818 5:19481171 C ENSESTG00000029018 ENSESTT00000073115 Transcript intron_variant - - - - - - rs2972818 5:19481171 C CCDS3889.1 CCDS3889.1 Transcript intron_variant - - - - - - rs2972818 5:19481171 C 1016 NM_004934.3 Transcript intron_variant - - - - - - rs1689681 5:19533899 T CCDS54835.1 CCDS54835.1 Transcript intron_variant - - - - - - rs1689681 5:19533899 T 1016 NM_001167667.1 Transcript intron_variant - - - - - - rs1689681 5:19533899 T ENSESTG00000029018 ENSESTT00000073129 Transcript intron_variant - - - - - - rs1689681 5:19533899 T ENSESTG00000029018 ENSESTT00000073115 Transcript intron_variant - - - - - - rs1689681 5:19533899 T ENSESTG00000029018 ENSESTT00000073139 Transcript intron_variant - - - - - - rs1689681 5:19533899 T CCDS3889.1 CCDS3889.1 Transcript intron_variant - - - - - - rs1689681 5:19533899 T 1016 NM_004934.3 Transcript intron_variant - - - - - - rs4242064 5:19639633 G CCDS54835.1 CCDS54835.1 Transcript intron_variant - - - - - - rs4242064 5:19639633 G 1016 NM_001167667.1 Transcript intron_variant - - - - - - rs4242064 5:19639633 G CCDS3889.1 CCDS3889.1 Transcript intron_variant - - - - - - rs4242064 5:19639633 G 1016 NM_004934.3 Transcript intron_variant - - - - - - rs10805651 5:19795093 C CCDS54835.1 CCDS54835.1 Transcript intron_variant - - - - - - rs10805651 5:19795093 C 1016 NM_001167667.1 Transcript intron_variant - - - - - - rs10805651 5:19795093 C ENSESTG00000028982 ENSESTT00000073010 Transcript intron_variant - - - - - - rs10805651 5:19795093 C ENSESTG00000028982 ENSESTT00000072958 Transcript intron_variant - - - - - - rs10805651 5:19795093 C CCDS3889.1 CCDS3889.1 Transcript intron_variant - - - - - - rs10805651 5:19795093 C 1016 NM_004934.3 Transcript intron_variant - - - - - - rs10941487 5:19795265 C CCDS54835.1 CCDS54835.1 Transcript intron_variant - - - - - - rs10941487 5:19795265 C 1016 NM_001167667.1 Transcript intron_variant - - - - - - rs10941487 5:19795265 C ENSESTG00000028982 ENSESTT00000073010 Transcript intron_variant - - - - - - rs10941487 5:19795265 C ENSESTG00000028982 ENSESTT00000072958 Transcript intron_variant - - - - - - rs10941487 5:19795265 C CCDS3889.1 CCDS3889.1 Transcript intron_variant - - - - - - rs10941487 5:19795265 C 1016 NM_004934.3 Transcript intron_variant - - - - - - rs4419596 5:19798799 C CCDS54835.1 CCDS54835.1 Transcript intron_variant - - - - - - rs4419596 5:19798799 C 1016 NM_001167667.1 Transcript intron_variant - - - - - - rs4419596 5:19798799 C ENSESTG00000028982 ENSESTT00000073010 Transcript intron_variant - - - - - - rs4419596 5:19798799 C ENSESTG00000028982 ENSESTT00000072958 Transcript intron_variant - - - - - - rs4419596 5:19798799 C CCDS3889.1 CCDS3889.1 Transcript intron_variant - - - - - - rs4419596 5:19798799 C 1016 NM_004934.3 Transcript intron_variant - - - - - - rs7729153 5:19839443 C 1016 NM_001167667.1 Transcript intron_variant - - - - - - rs7729153 5:19839443 C ENSESTG00000028982 ENSESTT00000072999 Transcript intron_variant - - - - - - rs7729153 5:19839443 C ENSESTG00000028982 ENSESTT00000072974 Transcript intron_variant - - - - - - rs7729153 5:19839443 C ENSESTG00000028982 ENSESTT00000072989 Transcript intron_variant - - - - - - rs7729153 5:19839443 C 1016 NM_004934.3 Transcript intron_variant - - - - - - rs7729153 5:19839443 C CCDS54835.1 CCDS54835.1 Transcript upstream_gene_variant - - - - - - DISTANCE=348 rs7729153 5:19839443 C ENSESTG00000028982 ENSESTT00000072958 Transcript intron_variant - - - - - - rs7729153 5:19839443 C CCDS3889.1 CCDS3889.1 Transcript upstream_gene_variant - - - - - - DISTANCE=348 rs4866158 5:19886992 A 1016 NM_001167667.1 Transcript intron_variant - - - - - - rs4866158 5:19886992 A ENSESTG00000028982 ENSESTT00000072974 Transcript upstream_gene_variant - - - - - - DISTANCE=611 rs4866158 5:19886992 A ENSESTG00000028982 ENSESTT00000072958 Transcript intron_variant - - - - - - rs4866158 5:19886992 A 1016 NM_004934.3 Transcript intron_variant - - - - - - rs9292829 5:19978850 T 1016 NM_001167667.1 Transcript intron_variant - - - - - - rs9292829 5:19978850 T ENSESTG00000028982 ENSESTT00000072958 Transcript intron_variant - - - - - - rs9292829 5:19978850 T 1016 NM_004934.3 Transcript intron_variant - - - - - - rs4329022 5:20199941 C - - - intergenic_variant - - - - - - rs6451730 5:20207087 T - - - intergenic_variant - - - - - - rs4431347 5:20216654 A - - - intergenic_variant - - - - - - rs2457037 5:20471484 C - - - intergenic_variant - - - - - - rs145794798 5:20738063 A - - - intergenic_variant - - - - - - rs6451925 5:20986096 C - - - intergenic_variant - - - - - - rs4866255 5:21005067 A - - - intergenic_variant - - - - - - rs10462125 5:21010536 T - - - intergenic_variant - - - - - - rs4621591 5:21020049 C - - - intergenic_variant - - - - - - rs10064794 5:21090870 A - - - intergenic_variant - - - - - - rs294737 5:21206083 T - - - intergenic_variant - - - - - - rs1388573 5:21240576 A - - - intergenic_variant - - - - - - rs4866273 5:21268562 C - - - intergenic_variant - - - - - - rs7736806 5:21427717 G - - - intergenic_variant - - - - - - rs10077869 5:21726058 A - - - intergenic_variant - - - - - - rs2966948 5:22395653 C ENSESTG00000025608 ENSESTT00000064551 Transcript intron_variant - - - - - - rs2966948 5:22395653 C ENSESTG00000025608 ENSESTT00000064580 Transcript intron_variant - - - - - - rs2966948 5:22395653 C ENSESTG00000025608 ENSESTT00000064616 Transcript intron_variant - - - - - - rs2966948 5:22395653 C 1010 NM_004061.3 Transcript intron_variant - - - - - - rs6888018 5:22450726 T ENSESTG00000025608 ENSESTT00000064551 Transcript intron_variant - - - - - - rs6888018 5:22450726 T ENSESTG00000025608 ENSESTT00000064580 Transcript intron_variant - - - - - - rs6888018 5:22450726 T ENSESTG00000025608 ENSESTT00000064616 Transcript intron_variant - - - - - - rs6888018 5:22450726 T 1010 NM_004061.3 Transcript intron_variant - - - - - - rs4604154 5:22626198 C ENSESTG00000025608 ENSESTT00000064551 Transcript intron_variant - - - - - - rs4604154 5:22626198 C 1010 NM_004061.3 Transcript intron_variant - - - - - - rs780184 5:22801132 G 1010 NM_004061.3 Transcript intron_variant - - - - - - rs9293087 5:23667760 G - - - intergenic_variant - - - - - - rs1949615 5:23704125 T - - - intergenic_variant - - - - - - rs6890231 5:23705989 A - - - intergenic_variant - - - - - - rs319606 5:23855113 T - - - intergenic_variant - - - - - - rs2134239 5:23969633 A ENSESTG00000005991 ENSESTT00000015175 Transcript downstream_gene_variant - - - - - - DISTANCE=1918 rs1428548 5:24129662 C - - - intergenic_variant - - - - - - rs10059387 5:24289433 T - ENSR00001276837 RegulatoryFeature regulatory_region_variant - - - - - - rs10059387 5:24289433 T - - - intergenic_variant - - - - - - rs6869681 5:24630786 A 1008 NM_006727.3 Transcript intron_variant - - - - - - rs6869681 5:24630786 A ENSESTG00000023214 ENSESTT00000058754 Transcript intron_variant - - - - - - rs1910963 5:24632589 C 1008 NM_006727.3 Transcript intron_variant - - - - - - rs1910963 5:24632589 C ENSESTG00000023214 ENSESTT00000058754 Transcript intron_variant - - - - - - rs11747572 5:24722446 G - - - intergenic_variant - - - - - - rs7703203 5:25424600 T ENSESTG00000016916 ENSESTT00000042425 Transcript upstream_gene_variant - - - - - - DISTANCE=1634 rs7703203 5:25424600 T ENSESTG00000016916 ENSESTT00000042429 Transcript upstream_gene_variant - - - - - - DISTANCE=1634 rs2126964 5:25457455 T - - - intergenic_variant - - - - - - rs561230 5:25682479 A - - - intergenic_variant - - - - - - rs4296768 5:25955537 T - - - intergenic_variant - - - - - - rs1541080 5:26085067 T - - - intergenic_variant - - - - - - rs7728781 5:26201828 A - - - intergenic_variant - - - - - - rs1411579 5:26206032 C - - - intergenic_variant - - - - - - rs4701267 5:26355440 T - - - intergenic_variant - - - - - - rs1469448 5:26511340 G - - - intergenic_variant - - - - - - rs2029908 5:26643633 G - - - intergenic_variant - - - - - - rs9885269 5:26657631 C - - - intergenic_variant - - - - - - rs6452371 5:27074514 T - - - intergenic_variant - - - - - - rs10079299 5:27215869 G - - - intergenic_variant - - - - - - rs2561645 5:27413410 T - - - intergenic_variant - - - - - - rs7449313 5:27635042 A - - - intergenic_variant - - - - - - rs7447440 5:27654226 C - - - intergenic_variant - - - - - - rs10035356 5:27714252 C - - - intergenic_variant - - - - - - rs10042313 5:27756239 T - - - intergenic_variant - - - - - - rs6890003 5:27804636 A - - - intergenic_variant - - - - - - rs4380676 5:27817267 A - - - intergenic_variant - - - - - - rs7445313 5:27851054 A - - - intergenic_variant - - - - - - rs6880341 5:27851833 T - - - intergenic_variant - - - - - - rs4610469 5:28131366 G - - - intergenic_variant - - - - - - rs10073640 5:28152314 G - - - intergenic_variant - - - - - - rs3928220 5:28974973 T - - - intergenic_variant - - - - - - rs10472664 5:28998704 T ENSESTG00000000287 ENSESTT00000000692 Transcript downstream_gene_variant - - - - - - DISTANCE=3732 rs6892751 5:29012196 C - - - intergenic_variant - - - - - - rs509297 5:29043069 G - - - intergenic_variant - - - - - - rs504032 5:29048986 A - - - intergenic_variant - - - - - - rs2644939 5:29066523 G - - - intergenic_variant - - - - - - rs613692 5:29067431 T - - - intergenic_variant - - - - - - rs309673 5:29105015 G - - - intergenic_variant - - - - - - rs181847 5:29130090 G - - - intergenic_variant - - - - - - rs6450688 5:29339203 T - - - intergenic_variant - - - - - - rs3114510 5:29714558 A - - - intergenic_variant - - - - - - rs7727420 5:30181947 T - - - intergenic_variant - - - - - - rs4440376 5:30258038 A - - - intergenic_variant - - - - - - rs10038353 5:30356337 G - - - intergenic_variant - - - - - - rs7449139 5:30377363 T - - - intergenic_variant - - - - - - rs2330538 5:30765098 G - ENSR00001277318 RegulatoryFeature regulatory_region_variant - - - - - - rs2330538 5:30765098 G - - - intergenic_variant - - - - - - rs1995271 5:30782816 C - - - intergenic_variant - - - - - - rs1604098 5:30816441 T - - - intergenic_variant - - - - - - rs2962790 5:31322851 G CCDS3894.1 CCDS3894.1 Transcript intron_variant - - - - - - rs2962790 5:31322851 G ENSESTG00000023561 ENSESTT00000059550 Transcript intron_variant - - - - - - rs2962790 5:31322851 G 1004 NM_004932.3 Transcript intron_variant - - - - - - rs2962790 5:31322851 G ENSESTG00000023561 ENSESTT00000059589 Transcript intron_variant - - - - - - rs1678904 5:31671320 C - - - intergenic_variant - - - - - - rs1995362 5:31889478 C - ENSR00001277453 RegulatoryFeature regulatory_region_variant - - - - - - rs1995362 5:31889478 C CCDS34137.1 CCDS34137.1 Transcript intron_variant - - - - - - rs1995362 5:31889478 C ENSESTG00000023765 ENSESTT00000059926 Transcript intron_variant - - - - - - rs1995362 5:31889478 C 23037 NM_178140.2 Transcript intron_variant - - - - - - rs818124 5:32658745 G - - - intergenic_variant - - - - - - rs818127 5:32692555 A - ENSR00001408250 RegulatoryFeature regulatory_region_variant - - - - - - rs818127 5:32692555 A - - - intergenic_variant - - - - - - rs297614 5:34114410 C ENSESTG00000027211 ENSESTT00000068558 Transcript intron_variant - - - - - - rs1440437 5:34384539 C - - - intergenic_variant - - - - - - rs37378 5:35045712 T ENSESTG00000006910 ENSESTT00000017585 Transcript intron_variant - - - - - - rs37378 5:35045712 T CCDS3908.1 CCDS3908.1 Transcript intron_variant - - - - - - rs37378 5:35045712 T 5618 NR_037910.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3149 rs37378 5:35045712 T 5618 NM_001204318.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3149 rs37378 5:35045712 T 5618 NM_001204316.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3149 rs37378 5:35045712 T CCDS56360.1 CCDS56360.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3790 rs37378 5:35045712 T 64902 NM_031900.3 Transcript intron_variant - - - - - - rs37378 5:35045712 T ENSESTG00000006910 ENSESTT00000017574 Transcript intron_variant - - - - - - rs37378 5:35045712 T CCDS56359.1 CCDS56359.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3680 rs37378 5:35045712 T 5618 NM_001204317.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3149 rs37378 5:35045712 T CCDS56361.1 CCDS56361.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3680 rs37378 5:35045712 T ENSESTG00000006910 ENSESTT00000017593 Transcript intron_variant - - - - - - rs37365 5:35072213 T 5618 NR_037910.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs37365 5:35072213 T CCDS56360.1 CCDS56360.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T 5618 NM_000949.5 Transcript intron_variant - - - - - - rs37365 5:35072213 T CCDS56362.1 CCDS56362.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T CCDS3909.1 CCDS3909.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T CCDS56359.1 CCDS56359.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T CCDS56361.1 CCDS56361.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T CCDS56358.1 CCDS56358.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T ENSESTG00000006874 ENSESTT00000017501 Transcript intron_variant - - - - - - rs37365 5:35072213 T 5618 NM_001204315.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T 5618 NM_001204316.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T 5618 NM_001204318.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T ENSESTG00000006874 ENSESTT00000017521 Transcript downstream_gene_variant - - - - - - DISTANCE=523 rs37365 5:35072213 T 5618 NM_001204314.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T 5618 NM_001204317.1 Transcript intron_variant - - - - - - rs37365 5:35072213 T ENSESTG00000006874 ENSESTT00000017490 Transcript downstream_gene_variant - - - - - - DISTANCE=594 rs1587604 5:35266477 T - - - intergenic_variant - - - - - - rs176270 5:35614560 T 79925 NM_024867.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3429 rs176270 5:35614560 T ENSESTG00000006762 ENSESTT00000017187 Transcript upstream_gene_variant - - - - - - DISTANCE=3462 rs176270 5:35614560 T 79925 NM_144722.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3429 rs176270 5:35614560 T CCDS43309.1 CCDS43309.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3540 rs176270 5:35614560 T CCDS3910.1 CCDS3910.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3540 rs176270 5:35614560 T ENSESTG00000006762 ENSESTT00000017179 Transcript upstream_gene_variant - - - - - - DISTANCE=3437 rs6414880 5:35931635 G 133690 NM_144647.3 Transcript intron_variant - - - - - - rs6414880 5:35931635 G ENSESTG00000006856 ENSESTT00000017438 Transcript intron_variant - - - - - - rs6414880 5:35931635 G ENSESTG00000006856 ENSESTT00000017434 Transcript intron_variant - - - - - - rs6414880 5:35931635 G 133690 NM_001042625.1 Transcript intron_variant - - - - - - rs2453302 5:36039441 G 167127 NM_001168316.1 Transcript intron_variant - - - - - - rs2453302 5:36039441 G CCDS3914.1 CCDS3914.1 Transcript intron_variant - - - - - - rs2453302 5:36039441 G ENSESTG00000025537 ENSESTT00000064520 Transcript downstream_gene_variant - - - - - - DISTANCE=193 rs2453302 5:36039441 G CCDS54842.1 CCDS54842.1 Transcript intron_variant - - - - - - rs2453302 5:36039441 G 167127 NR_031764.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2453302 5:36039441 G ENSESTG00000025537 ENSESTT00000064403 Transcript downstream_gene_variant - - - - - - DISTANCE=321 rs2453302 5:36039441 G 167127 NM_174914.3 Transcript intron_variant - - - - - - rs33673 5:36153837 A CCDS3915.1 CCDS3915.1 Transcript intron_variant - - - - - - rs33673 5:36153837 A ENSESTG00000025123 ENSESTT00000063560 Transcript intron_variant - - - - - - rs33673 5:36153837 A 6502 NM_032637.3 Transcript intron_variant - - - - - - rs33673 5:36153837 A 6502 NM_001243120.1 Transcript intron_variant - - - - - - rs33673 5:36153837 A 92255 NM_001007527.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1822 rs33673 5:36153837 A 6502 NM_005983.3 Transcript intron_variant - - - - - - rs33673 5:36153837 A ENSESTG00000025123 ENSESTT00000063578 Transcript intron_variant - - - - - - rs33673 5:36153837 A ENSESTG00000025123 ENSESTT00000063434 Transcript intron_variant - - - - - - rs33673 5:36153837 A CCDS3916.1 CCDS3916.1 Transcript intron_variant - - - - - - rs33673 5:36153837 A ENSESTG00000025123 ENSESTT00000063548 Transcript intron_variant - - - - - - rs33673 5:36153837 A ENSESTG00000025123 ENSESTT00000063397 Transcript intron_variant - - - - - - rs77437359 5:36286948 C CCDS3918.1 CCDS3918.1 Transcript intron_variant - - - - - - rs77437359 5:36286948 C ENSESTG00000025396 ENSESTT00000064110 Transcript intron_variant - - - - - - rs77437359 5:36286948 C ENSESTG00000025396 ENSESTT00000064077 Transcript intron_variant - - - - - - rs77437359 5:36286948 C 202151 NM_001161429.1 Transcript intron_variant - - - - - - rs77437359 5:36286948 C CCDS54843.1 CCDS54843.1 Transcript intron_variant - - - - - - rs77437359 5:36286948 C 202151 NM_145000.3 Transcript intron_variant - - - - - - rs2455268 5:36443023 T - ENSR00001278220 RegulatoryFeature regulatory_region_variant - - - - - - rs2455268 5:36443023 T - - - intergenic_variant - - - - - - rs292177 5:36833330 G - - - intergenic_variant - - - - - - rs296956 5:36891874 G 25836 NM_015384.4 Transcript intron_variant - - - - - - rs296956 5:36891874 G 25836 NM_133433.3 Transcript intron_variant - - - - - - rs296956 5:36891874 G ENSESTG00000025342 ENSESTT00000064016 Transcript intron_variant - - - - - - rs296957 5:36959810 A 25836 NM_015384.4 Transcript intron_variant - - - - - - rs296957 5:36959810 A CCDS47198.1 CCDS47198.1 Transcript intron_variant - - - - - - rs296957 5:36959810 A CCDS3920.1 CCDS3920.1 Transcript intron_variant - - - - - - rs296957 5:36959810 A 25836 NM_133433.3 Transcript intron_variant - - - - - - rs296957 5:36959810 A ENSESTG00000025342 ENSESTT00000064016 Transcript intron_variant - - - - - - rs6876576 5:37247700 A CCDS34146.2 CCDS34146.2 Transcript intron_variant - - - - - - rs6876576 5:37247700 A ENSESTG00000006339 ENSESTT00000016001 Transcript upstream_gene_variant - - - - - - DISTANCE=1450 rs6876576 5:37247700 A 65250 NM_023073.3 Transcript intron_variant - - - - - - rs6876576 5:37247700 A ENSESTG00000006453 ENSESTT00000016263 Transcript upstream_gene_variant - - - - - - DISTANCE=3183 rs593170 5:37568103 A ENSESTG00000006374 ENSESTT00000016112 Transcript intron_variant - - - - - - rs593170 5:37568103 A 55100 NM_018034.2 Transcript intron_variant - - - - - - rs593170 5:37568103 A CCDS34147.1 CCDS34147.1 Transcript intron_variant - - - - - - rs593170 5:37568103 A ENSESTG00000006374 ENSESTT00000016107 Transcript intron_variant - - - - - - rs10035139 5:37960344 A ENSESTG00000006395 ENSESTT00000016127 Transcript intron_variant - - - - - - rs7727456 5:38155551 C ENSESTG00000033417 ENSESTT00000084396 Transcript intron_variant - - - - - - rs2262981 5:38274487 G 133584 NM_152403.3 Transcript intron_variant - - - - - - rs2262981 5:38274487 G ENSESTG00000033449 ENSESTT00000084589 Transcript intron_variant - - - - - - rs2262981 5:38274487 G 133584 NM_001205301.1 Transcript intron_variant - - - - - - rs2262981 5:38274487 G CCDS56363.1 CCDS56363.1 Transcript intron_variant - - - - - - rs2262981 5:38274487 G CCDS3924.1 CCDS3924.1 Transcript intron_variant - - - - - - rs2914239 5:38623112 A - - - intergenic_variant - - - - - - rs327283 5:38639549 C - - - intergenic_variant - - - - - - rs6892483 5:38808058 A - ENSR00001278576 RegulatoryFeature regulatory_region_variant - - - - - - rs6892483 5:38808058 A ENSESTG00000033675 ENSESTT00000085117 Transcript intron_variant - - - - - - rs6892483 5:38808058 A ENSESTG00000033675 ENSESTT00000085123 Transcript intron_variant - - - - - - rs1239275 5:39009761 T ENSESTG00000020623 ENSESTT00000051888 Transcript intron_variant - - - - - - rs1239275 5:39009761 T 253260 NM_152756.3 Transcript intron_variant - - - - - - rs1239275 5:39009761 T ENSESTG00000020623 ENSESTT00000051898 Transcript intron_variant - - - - - - rs1239275 5:39009761 T CCDS34148.1 CCDS34148.1 Transcript intron_variant - - - - - - rs452039 5:39086352 G - - - intergenic_variant - - - - - - rs1469467 5:39178094 A - ENSR00001278652 RegulatoryFeature regulatory_region_variant - - - - - - rs1469467 5:39178094 A ENSESTG00000020562 ENSESTT00000051600 Transcript intron_variant - - - - - - rs1469467 5:39178094 A CCDS54848.1 CCDS54848.1 Transcript intron_variant - - - - - - rs1469467 5:39178094 A 2533 NM_001243093.1 Transcript intron_variant - - - - - - rs1469467 5:39178094 A 2533 NM_001465.4 Transcript intron_variant - - - - - - rs1469467 5:39178094 A ENSESTG00000020562 ENSESTT00000051636 Transcript intron_variant - - - - - - rs1469467 5:39178094 A 2533 NM_199335.3 Transcript intron_variant - - - - - - rs1469467 5:39178094 A ENSESTG00000020562 ENSESTT00000051625 Transcript intron_variant - - - - - - rs1469467 5:39178094 A CCDS47200.1 CCDS47200.1 Transcript intron_variant - - - - - - rs1469467 5:39178094 A CCDS58945.1 CCDS58945.1 Transcript intron_variant - - - - - - rs700189 5:39216326 T - ENSR00001278664 RegulatoryFeature regulatory_region_variant - - - - - - rs700189 5:39216326 T ENSESTG00000020562 ENSESTT00000051600 Transcript intron_variant - - - - - - rs700189 5:39216326 T ENSESTG00000020562 ENSESTT00000051582 Transcript intron_variant - - - - - - rs700189 5:39216326 T 2533 NM_001243093.1 Transcript intron_variant - - - - - - rs700189 5:39216326 T 2533 NM_001465.4 Transcript intron_variant - - - - - - rs700189 5:39216326 T ENSESTG00000020562 ENSESTT00000051567 Transcript intron_variant - - - - - - rs700189 5:39216326 T 2533 NM_199335.3 Transcript intron_variant - - - - - - rs700189 5:39216326 T ENSESTG00000020562 ENSESTT00000051625 Transcript intron_variant - - - - - - rs700189 5:39216326 T ENSESTG00000020562 ENSESTT00000051549 Transcript intron_variant - - - - - - rs700189 5:39216326 T CCDS58945.1 CCDS58945.1 Transcript intron_variant - - - - - - rs1260811 5:39605674 C - - - intergenic_variant - - - - - - rs568633 5:39935906 C - - - intergenic_variant - - - - - - rs355737 5:39946438 T - - - intergenic_variant - - - - - - rs355736 5:39946640 G - - - intergenic_variant - - - - - - rs431137 5:39952569 G - - - intergenic_variant - - - - - - rs355724 5:39957563 T - - - intergenic_variant - - - - - - rs1697894 5:39962825 T - - - intergenic_variant - - - - - - rs422382 5:39963145 T - - - intergenic_variant - - - - - - rs405385 5:39970137 A - - - intergenic_variant - - - - - - rs1605200 5:39979839 G - - - intergenic_variant - - - - - - rs2939377 5:39982325 A - - - intergenic_variant - - - - - - rs2860514 5:39986201 T - - - intergenic_variant - - - - - - rs6860096 5:39988546 G - - - intergenic_variant - - - - - - rs1506186 5:40015602 A - - - intergenic_variant - - - - - - rs1857873 5:40023258 A - - - intergenic_variant - - - - - - rs1395156 5:40058015 A - - - intergenic_variant - - - - - - rs2939380 5:40064957 G - - - intergenic_variant - - - - - - rs1354696 5:40079887 T - - - intergenic_variant - - - - - - rs1158839 5:40083282 T - - - intergenic_variant - - - - - - rs2059756 5:40098870 G - - - intergenic_variant - - - - - - rs1506182 5:40113866 T - - - intergenic_variant - - - - - - rs10043409 5:40120276 C - - - intergenic_variant - - - - - - rs4957119 5:40129041 C - - - intergenic_variant - - - - - - rs348591 5:40318045 C - - - intergenic_variant - - - - - - rs6451506 5:40457889 G - - - intergenic_variant - - - - - - rs6883381 5:40949015 T 730 NM_000587.2 Transcript intron_variant - - - - - - rs6883381 5:40949015 T CCDS47201.1 CCDS47201.1 Transcript intron_variant - - - - - - rs6883381 5:40949015 T ENSESTG00000013515 ENSESTT00000033909 Transcript intron_variant - - - - - - rs6883381 5:40949015 T ENSESTG00000013515 ENSESTT00000033895 Transcript intron_variant - - - - - - rs1349372 5:41001682 G CCDS47202.1 CCDS47202.1 Transcript intron_variant - - - - - - rs1349372 5:41001682 G 133558 NM_173489.4 Transcript intron_variant - - - - - - rs1349372 5:41001682 G ENSESTG00000013515 ENSESTT00000033895 Transcript intron_variant - - - - - - rs445682 5:41098290 C - - - intergenic_variant - - - - - - rs325877 5:41109229 T - ENSR00001278967 RegulatoryFeature regulatory_region_variant - - - - - - rs325877 5:41109229 T - - - intergenic_variant - - - - - - rs320605 5:41320222 C CCDS34150.1 CCDS34150.1 Transcript intron_variant - - - - - - rs320605 5:41320222 C 345557 NM_001005473.2 Transcript intron_variant - - - - - - rs10078450 5:42214839 T - - - intergenic_variant - - - - - - rs6881244 5:42303629 G - - - intergenic_variant - - - - - - rs4552612 5:42519982 C 2690 NM_000163.4 Transcript intron_variant - - - - - - rs4552612 5:42519982 C 2690 NM_001242400.2 Transcript intron_variant - - - - - - rs4552612 5:42519982 C ENSESTG00000003400 ENSESTT00000008506 Transcript intron_variant - - - - - - rs4552612 5:42519982 C 2690 NM_001242399.2 Transcript intron_variant - - - - - - rs4552612 5:42519982 C 2690 NM_001242401.3 Transcript intron_variant - - - - - - rs4552612 5:42519982 C ENSESTG00000003400 ENSESTT00000008509 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242461.1 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242400.2 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242405.2 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242406.2 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242399.2 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242462.1 Transcript intron_variant - - - - - - rs10041109 5:42705683 G CCDS56364.1 CCDS56364.1 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242403.2 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242404.2 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242460.1 Transcript intron_variant - - - - - - rs10041109 5:42705683 G CCDS3940.1 CCDS3940.1 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242402.2 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_000163.4 Transcript intron_variant - - - - - - rs10041109 5:42705683 G 2690 NM_001242401.3 Transcript intron_variant - - - - - - rs7710962 5:42745629 T - ENSR00001279099 RegulatoryFeature regulatory_region_variant - - - - - - rs7710962 5:42745629 T - - - intergenic_variant - - - - - - rs2548344 5:42977935 G - - - intergenic_variant - - - - - - rs10050506 5:43141780 G 7690 NM_003432.1 Transcript intron_variant - - - - - - rs10050506 5:43141780 G ENSESTG00000019230 ENSESTT00000048332 Transcript intron_variant - - - - - - rs10050506 5:43141780 G CCDS43313.1 CCDS43313.1 Transcript intron_variant - - - - - - rs10050506 5:43141780 G ENSESTG00000019192 ENSESTT00000048299 Transcript downstream_gene_variant - - - - - - DISTANCE=2447 rs6885937 5:43149519 A 7690 NM_003432.1 Transcript intron_variant - - - - - - rs6885937 5:43149519 A ENSESTG00000019230 ENSESTT00000048332 Transcript intron_variant - - - - - - rs6885937 5:43149519 A CCDS43313.1 CCDS43313.1 Transcript intron_variant - - - - - - rs6451680 5:43230760 C ENSESTG00000019245 ENSESTT00000048376 Transcript intron_variant - - - - - - rs6451680 5:43230760 C 167359 NR_072980.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6451680 5:43230760 C ENSESTG00000019245 ENSESTT00000048364 Transcript intron_variant - - - - - - rs6451680 5:43230760 C 167359 NM_153361.3 Transcript intron_variant - - - - - - rs6873090 5:43238692 C ENSESTG00000019245 ENSESTT00000048376 Transcript intron_variant - - - - - - rs6873090 5:43238692 C 167359 NR_072980.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6873090 5:43238692 C ENSESTG00000019245 ENSESTT00000048364 Transcript intron_variant - - - - - - rs6873090 5:43238692 C 167359 NM_153361.3 Transcript intron_variant - - - - - - rs4866832 5:43515010 C - ENSR00001279284 RegulatoryFeature regulatory_region_variant - - - - - - rs4866832 5:43515010 C 375444 NM_198566.2 Transcript 5_prime_UTR_variant 264 - - - - - rs10055616 5:43594243 G ENSESTG00000019514 ENSESTT00000048984 Transcript intron_variant - - - - - - rs10055616 5:43594243 G 100652772 XM_003403422.1 Transcript intron_variant - - - - - - rs6859092 5:43851033 C - - - intergenic_variant - - - - - - rs7733767 5:44059277 A - - - intergenic_variant - - - - - - rs3112774 5:44221423 T - - - intergenic_variant - - - - - - rs1374971 5:44337480 A CCDS3950.1 CCDS3950.1 Transcript intron_variant - - - - - - rs1374971 5:44337480 A ENSESTG00000021744 ENSESTT00000054714 Transcript intron_variant - - - - - - rs1374971 5:44337480 A ENSESTG00000021744 ENSESTT00000054685 Transcript intron_variant - - - - - - rs1374971 5:44337480 A 2255 NM_004465.1 Transcript intron_variant - - - - - - rs1374971 5:44337480 A ENSESTG00000021744 ENSESTT00000054665 Transcript intron_variant - - - - - - rs2929854 5:44377083 T CCDS3950.1 CCDS3950.1 Transcript intron_variant - - - - - - rs2929854 5:44377083 T ENSESTG00000021744 ENSESTT00000054714 Transcript intron_variant - - - - - - rs2929854 5:44377083 T ENSESTG00000021744 ENSESTT00000054685 Transcript intron_variant - - - - - - rs2929854 5:44377083 T 2255 NM_004465.1 Transcript intron_variant - - - - - - rs2929854 5:44377083 T ENSESTG00000021744 ENSESTT00000054665 Transcript intron_variant - - - - - - rs2973648 5:44390447 C CCDS3950.1 CCDS3950.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1663 rs2973648 5:44390447 C ENSESTG00000021744 ENSESTT00000054714 Transcript upstream_gene_variant - - - - - - DISTANCE=962 rs2973648 5:44390447 C ENSESTG00000021744 ENSESTT00000054685 Transcript upstream_gene_variant - - - - - - DISTANCE=692 rs2973648 5:44390447 C 2255 NM_004465.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1663 rs2973648 5:44390447 C ENSESTG00000021744 ENSESTT00000054665 Transcript upstream_gene_variant - - - - - - DISTANCE=639 rs2929849 5:44408061 C - - - intergenic_variant - - - - - - rs2973654 5:44435216 A - - - intergenic_variant - - - - - - rs4280874 5:44451824 G - - - intergenic_variant - - - - - - rs2929857 5:44488554 G - - - intergenic_variant - - - - - - rs1821935 5:44701605 C ENSESTG00000021718 ENSESTT00000054542 Transcript upstream_gene_variant - - - - - - DISTANCE=735 rs10941688 5:44930005 T - - - intergenic_variant - - - - - - rs10079256 5:45135612 G - - - intergenic_variant - - - - - - rs6865031 5:45233655 A - - - intergenic_variant - - - - - - rs7444102 5:45405226 G 348980 NM_021072.3 Transcript intron_variant - - - - - - rs7444102 5:45405226 G CCDS3952.1 CCDS3952.1 Transcript intron_variant - - - - - - rs6451800 5:45405939 G 348980 NM_021072.3 Transcript intron_variant - - - - - - rs6451800 5:45405939 G CCDS3952.1 CCDS3952.1 Transcript intron_variant - - - - - - rs1463594 5:45436636 A 348980 NM_021072.3 Transcript intron_variant - - - - - - rs1463594 5:45436636 A CCDS3952.1 CCDS3952.1 Transcript intron_variant - - - - - - rs10473385 5:45444557 T 348980 NM_021072.3 Transcript intron_variant - - - - - - rs10473385 5:45444557 T CCDS3952.1 CCDS3952.1 Transcript intron_variant - - - - - - rs7293500 5:46071542 G - - - intergenic_variant - - - - - - rs10073888 5:46072876 G - - - intergenic_variant - - - - - - rs4559000 5:46086413 G - - - intergenic_variant - - - - - - rs10472409 5:46099585 A - - - intergenic_variant - - - - - - rs2199091 5:49530641 C - - - intergenic_variant - - - - - - rs7715245 5:49954442 A - - - intergenic_variant - - - - - - rs27610 5:50166202 G - - - intergenic_variant - - - - - - rs27285 5:50197502 C - - - intergenic_variant - - - - - - rs27274 5:50244648 G - - - intergenic_variant - - - - - - rs1501986 5:50576689 G - - - intergenic_variant - - - - - - rs4865527 5:51399894 C - - - intergenic_variant - - - - - - rs4309926 5:51462447 G - ENSR00001279729 RegulatoryFeature regulatory_region_variant - - - - - - rs4309926 5:51462447 G - - - intergenic_variant - - - - - - rs2961724 5:51709376 A - - - intergenic_variant - - - - - - rs7710634 5:51804489 C - - - intergenic_variant - - - - - - rs6450065 5:51810071 G - - - intergenic_variant - - - - - - rs2447872 5:52221488 T ENSESTG00000024631 ENSESTT00000062593 Transcript downstream_gene_variant - - - - - - DISTANCE=168 rs2447872 5:52221488 T ENSESTG00000024631 ENSESTT00000062840 Transcript upstream_gene_variant - - - - - - DISTANCE=3965 rs2447872 5:52221488 T CCDS3955.1 CCDS3955.1 Transcript intron_variant - - - - - - rs2447872 5:52221488 T ENSESTG00000024631 ENSESTT00000062565 Transcript downstream_gene_variant - - - - - - DISTANCE=168 rs2447872 5:52221488 T 3672 NM_181501.1 Transcript intron_variant - - - - - - rs2447872 5:52221488 T ENSESTG00000024631 ENSESTT00000062396 Transcript downstream_gene_variant - - - - - - DISTANCE=168 rs2447872 5:52221488 T ENSESTG00000024631 ENSESTT00000062814 Transcript intron_variant - - - - - - rs27956 5:52338227 A ENSESTG00000024901 ENSESTT00000062965 Transcript intron_variant - - - - - - rs27956 5:52338227 A 3673 NM_002203.3 Transcript intron_variant - - - - - - rs27956 5:52338227 A CCDS3957.1 CCDS3957.1 Transcript intron_variant - - - - - - rs254612 5:52445483 C - - - intergenic_variant - - - - - - rs190394 5:52590141 T - - - intergenic_variant - - - - - - rs543476 5:52624925 G - - - intergenic_variant - - - - - - rs2042334 5:52753932 C - - - intergenic_variant - - - - - - rs389919 5:53005694 G - - - intergenic_variant - - - - - - rs198942 5:53039389 A - - - intergenic_variant - - - - - - rs271260 5:53174130 T ENSESTG00000024033 ENSESTT00000060668 Transcript intron_variant - - - - - - rs1363836 5:53219847 G CCDS54850.1 CCDS54850.1 Transcript intron_variant - - - - - - rs1363836 5:53219847 G 54622 NM_019087.2 Transcript intron_variant - - - - - - rs1363836 5:53219847 G ENSESTG00000024033 ENSESTT00000060668 Transcript intron_variant - - - - - - rs1823054 5:53997399 T - ENSR00001409340 RegulatoryFeature regulatory_region_variant - - - - - - rs1823054 5:53997399 T ENSESTG00000025407 ENSESTT00000064094 Transcript intron_variant - - - - - - rs1823054 5:53997399 T ENSESTG00000023910 ENSESTT00000060315 Transcript intron_variant - - - - - - rs1823054 5:53997399 T ENSESTG00000023910 ENSESTT00000060321 Transcript intron_variant - - - - - - rs4865589 5:54234136 C - - - intergenic_variant - - - - - - rs4482862 5:54876612 C - - - intergenic_variant - - - - - - rs7445404 5:55105288 C 54514 NM_001166534.1 Transcript intron_variant - - - - - - rs7445404 5:55105288 C 54514 NM_024415.2 Transcript intron_variant - - - - - - rs7445404 5:55105288 C 54514 NM_001142549.1 Transcript intron_variant - - - - - - rs7445404 5:55105288 C CCDS54855.1 CCDS54855.1 Transcript intron_variant - - - - - - rs7445404 5:55105288 C CCDS3969.1 CCDS3969.1 Transcript intron_variant - - - - - - rs7445404 5:55105288 C CCDS47208.1 CCDS47208.1 Transcript intron_variant - - - - - - rs7445404 5:55105288 C 54514 NM_001166533.1 Transcript intron_variant - - - - - - rs7445404 5:55105288 C CCDS54854.1 CCDS54854.1 Transcript intron_variant - - - - - - rs318818 5:55398269 C 79722 NM_024669.2 Transcript intron_variant - - - - - - rs318818 5:55398269 C CCDS34161.1 CCDS34161.1 Transcript intron_variant - - - - - - rs318818 5:55398269 C ENSESTG00000012495 ENSESTT00000031378 Transcript intron_variant - - - - - - rs298653 5:55462169 C 79722 NM_024669.2 Transcript intron_variant - - - - - - rs298653 5:55462169 C ENSESTG00000012495 ENSESTT00000031361 Transcript intron_variant - - - - - - rs298653 5:55462169 C CCDS34161.1 CCDS34161.1 Transcript intron_variant - - - - - - rs298653 5:55462169 C ENSESTG00000012495 ENSESTT00000031378 Transcript intron_variant - - - - - - rs2652476 5:55964994 G - ENSR00001280594 RegulatoryFeature regulatory_region_variant - - - - - - rs2652476 5:55964994 G - - - intergenic_variant - - - - - - rs1544737 5:56526565 T ENSESTG00000034562 ENSESTT00000087487 Transcript intron_variant - - - - - - rs1544737 5:56526565 T 65056 NM_001127236.2 Transcript intron_variant - - - - - - rs1544737 5:56526565 T CCDS47212.2 CCDS47212.2 Transcript intron_variant - - - - - - rs1544737 5:56526565 T 65056 NM_001127235.2 Transcript intron_variant - - - - - - rs1544737 5:56526565 T CCDS34162.1 CCDS34162.1 Transcript intron_variant - - - - - - rs1544737 5:56526565 T CCDS47211.1 CCDS47211.1 Transcript intron_variant - - - - - - rs1544737 5:56526565 T 65056 NM_001203246.1 Transcript intron_variant - - - - - - rs1544737 5:56526565 T 65056 NM_022913.3 Transcript intron_variant - - - - - - rs1544737 5:56526565 T ENSESTG00000034562 ENSESTT00000087492 Transcript intron_variant - - - - - - rs1544737 5:56526565 T ENSESTG00000034562 ENSESTT00000087473 Transcript intron_variant - - - - - - rs1544737 5:56526565 T ENSESTG00000034562 ENSESTT00000087481 Transcript intron_variant - - - - - - rs1544737 5:56526565 T ENSESTG00000034562 ENSESTT00000087489 Transcript intron_variant - - - - - - rs1994933 5:56762982 C ENSESTG00000034614 ENSESTT00000087543 Transcript intron_variant - - - - - - rs854131 5:56925651 T - - - intergenic_variant - - - - - - rs37531 5:57570602 T - - - intergenic_variant - - - - - - rs702713 5:57764231 T - - - intergenic_variant - - - - - - rs416657 5:57947637 C ENSESTG00000018777 ENSESTT00000047368 Transcript intron_variant - - - - - - rs416657 5:57947637 C CCDS3976.1 CCDS3976.1 Transcript intron_variant - - - - - - rs416657 5:57947637 C 115827 NM_138453.2 Transcript intron_variant - - - - - - rs256120 5:58595281 T - ENSR00001281026 RegulatoryFeature regulatory_region_variant - - - - - - rs256120 5:58595281 T 5144 NM_001165899.1 Transcript intron_variant - - - - - - rs256120 5:58595281 T 5144 NM_001197218.1 Transcript intron_variant - - - - - - rs256120 5:58595281 T CCDS47213.1 CCDS47213.1 Transcript intron_variant - - - - - - rs256120 5:58595281 T 5144 NM_001104631.1 Transcript intron_variant - - - - - - rs256120 5:58595281 T ENSESTG00000004978 ENSESTT00000012669 Transcript intron_variant - - - - - - rs256120 5:58595281 T 5144 NM_006203.4 Transcript intron_variant - - - - - - rs256120 5:58595281 T CCDS54858.1 CCDS54858.1 Transcript intron_variant - - - - - - rs256120 5:58595281 T ENSESTG00000004978 ENSESTT00000012679 Transcript intron_variant - - - - - - rs256120 5:58595281 T ENSESTG00000004978 ENSESTT00000012672 Transcript intron_variant - - - - - - rs256120 5:58595281 T 5144 NM_001197219.1 Transcript intron_variant - - - - - - rs256120 5:58595281 T CCDS56372.1 CCDS56372.1 Transcript intron_variant - - - - - - rs256120 5:58595281 T CCDS56373.1 CCDS56373.1 Transcript intron_variant - - - - - - rs256120 5:58595281 T ENSESTG00000004978 ENSESTT00000012665 Transcript intron_variant - - - - - - rs256120 5:58595281 T CCDS54859.1 CCDS54859.1 Transcript intron_variant - - - - - - rs6450539 5:59327685 G ENSESTG00000010796 ENSESTT00000027036 Transcript intron_variant - - - - - - rs6450539 5:59327685 G 5144 NM_001165899.1 Transcript intron_variant - - - - - - rs6450539 5:59327685 G ENSESTG00000010796 ENSESTT00000027039 Transcript intron_variant - - - - - - rs6450539 5:59327685 G ENSESTG00000010796 ENSESTT00000027027 Transcript intron_variant - - - - - - rs6450539 5:59327685 G CCDS54859.1 CCDS54859.1 Transcript intron_variant - - - - - - rs1823063 5:59895880 A 55789 NM_001145208.1 Transcript intron_variant - - - - - - rs1823063 5:59895880 A 55789 NM_018369.2 Transcript intron_variant - - - - - - rs1823063 5:59895880 A CCDS47214.1 CCDS47214.1 Transcript intron_variant - - - - - - rs1823063 5:59895880 A CCDS3977.1 CCDS3977.1 Transcript intron_variant - - - - - - rs2937625 5:61057893 C - - - intergenic_variant - - - - - - rs1875217 5:61122575 A - - - intergenic_variant - - - - - - rs263657 5:61216415 T - - - intergenic_variant - - - - - - rs6870781 5:61497789 G - - - intergenic_variant - - - - - - rs4235492 5:61581948 T - - - intergenic_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027306 Transcript intron_variant - - - - - - rs26640 5:61781127 A 51194 NM_016338.4 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027301 Transcript intron_variant - - - - - - rs26640 5:61781127 A CCDS47217.1 CCDS47217.1 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027351 Transcript downstream_gene_variant - - - - - - DISTANCE=1930 rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027330 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027298 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027343 Transcript intron_variant - - - - - - rs26640 5:61781127 A CCDS34167.1 CCDS34167.1 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027294 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027310 Transcript downstream_gene_variant - - - - - - DISTANCE=1930 rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027352 Transcript downstream_gene_variant - - - - - - DISTANCE=1930 rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027292 Transcript intron_variant - - - - - - rs26640 5:61781127 A 51194 NM_001134779.1 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027336 Transcript downstream_gene_variant - - - - - - DISTANCE=1930 rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027303 Transcript downstream_gene_variant - - - - - - DISTANCE=1930 rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027308 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027358 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027297 Transcript downstream_gene_variant - - - - - - DISTANCE=1930 rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027349 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027333 Transcript intron_variant - - - - - - rs26640 5:61781127 A ENSESTG00000010852 ENSESTT00000027355 Transcript intron_variant - - - - - - rs1306277 5:61986929 C - - - intergenic_variant - - - - - - rs168853 5:62820774 A - - - intergenic_variant - - - - - - rs4324629 5:62994133 C - - - intergenic_variant - - - - - - rs7703590 5:63320158 C - - - intergenic_variant - - - - - - rs2934801 5:63498521 T CCDS34169.1 CCDS34169.1 Transcript intron_variant - - - - - - rs2934801 5:63498521 T 285671 NM_178532.3 Transcript intron_variant - - - - - - rs2934801 5:63498521 T ENSESTG00000001460 ENSESTT00000003448 Transcript intron_variant - - - - - - rs2934801 5:63498521 T 285671 NM_001113561.1 Transcript intron_variant - - - - - - rs2934801 5:63498521 T ENSESTG00000001460 ENSESTT00000003446 Transcript intron_variant - - - - - - rs2934801 5:63498521 T CCDS47219.1 CCDS47219.1 Transcript intron_variant - - - - - - rs2934801 5:63498521 T ENSESTG00000001460 ENSESTT00000003449 Transcript intron_variant - - - - - - rs1445956 5:63554474 G 285671 NM_001113561.1 Transcript intron_variant - - - - - - rs1445956 5:63554474 G CCDS47219.1 CCDS47219.1 Transcript intron_variant - - - - - - rs4518331 5:63728650 A - - - intergenic_variant - - - - - - rs166706 5:64041591 G ENSESTG00000013175 ENSESTT00000033066 Transcript intron_variant - - - - - - rs166706 5:64041591 G CCDS34171.1 CCDS34171.1 Transcript intron_variant - - - - - - rs166706 5:64041591 G 285672 NM_173829.3 Transcript intron_variant - - - - - - rs266586 5:64328441 T - ENSR00001281645 RegulatoryFeature regulatory_region_variant - - - - - - rs266586 5:64328441 T - - - intergenic_variant - - - - - - rs7701492 5:64524124 T CCDS3983.2 CCDS3983.2 Transcript intron_variant - - - - - - rs7701492 5:64524124 T 11174 NM_197941.2 Transcript intron_variant - - - - - - rs966810 5:64560376 G CCDS3983.2 CCDS3983.2 Transcript intron_variant - - - - - - rs966810 5:64560376 G 11174 NM_197941.2 Transcript intron_variant - - - - - - rs786702 5:64649280 A CCDS3983.2 CCDS3983.2 Transcript intron_variant - - - - - - rs786702 5:64649280 A 11174 NM_197941.2 Transcript intron_variant - - - - - - rs786700 5:64678321 T CCDS3983.2 CCDS3983.2 Transcript intron_variant - - - - - - rs786700 5:64678321 T 11174 NM_197941.2 Transcript intron_variant - - - - - - rs786704 5:64716333 C CCDS3983.2 CCDS3983.2 Transcript intron_variant - - - - - - rs786704 5:64716333 C 11174 NM_197941.2 Transcript intron_variant - - - - - - rs10940042 5:64839380 A ENSESTG00000013146 ENSESTT00000032953 Transcript upstream_gene_variant - - - - - - DISTANCE=700 rs10940042 5:64839380 A ENSESTG00000013146 ENSESTT00000032950 Transcript intron_variant - - - - - - rs10940042 5:64839380 A 64105 NM_001267038.1 Transcript intron_variant - - - - - - rs10940042 5:64839380 A CCDS3984.1 CCDS3984.1 Transcript intron_variant - - - - - - rs10940042 5:64839380 A 64105 NM_022145.4 Transcript intron_variant - - - - - - rs438168 5:64855713 T ENSESTG00000013010 ENSESTT00000032663 Transcript upstream_gene_variant - - - - - - DISTANCE=3410 rs438168 5:64855713 T 23398 NR_046349.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3350 rs438168 5:64855713 T 64105 NM_001267038.1 Transcript intron_variant - - - - - - rs438168 5:64855713 T 23398 NR_046348.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3350 rs438168 5:64855713 T CCDS3985.1 CCDS3985.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3425 rs438168 5:64855713 T ENSESTG00000013010 ENSESTT00000032657 Transcript upstream_gene_variant - - - - - - DISTANCE=3410 rs438168 5:64855713 T 23398 NM_015342.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3350 rs438168 5:64855713 T ENSESTG00000013010 ENSESTT00000032643 Transcript upstream_gene_variant - - - - - - DISTANCE=3392 rs438168 5:64855713 T 23398 NR_046350.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3350 rs438168 5:64855713 T 64105 NM_022145.4 Transcript intron_variant - - - - - - rs438168 5:64855713 T CCDS3984.1 CCDS3984.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4979 rs438168 5:64855713 T ENSESTG00000013010 ENSESTT00000032640 Transcript upstream_gene_variant - - - - - - DISTANCE=3392 rs36223 5:64865975 T ENSESTG00000013010 ENSESTT00000032663 Transcript downstream_gene_variant - - - - - - DISTANCE=2186 rs36223 5:64865975 T 23398 NR_046349.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs36223 5:64865975 T ENSESTG00000013034 ENSESTT00000032685 Transcript upstream_gene_variant - - - - - - DISTANCE=2035 rs36223 5:64865975 T 23398 NR_046348.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs36223 5:64865975 T CCDS3985.1 CCDS3985.1 Transcript intron_variant - - - - - - rs36223 5:64865975 T ENSESTG00000013010 ENSESTT00000032657 Transcript downstream_gene_variant - - - - - - DISTANCE=150 rs36223 5:64865975 T 23398 NM_015342.3 Transcript intron_variant - - - - - - rs36223 5:64865975 T 23398 NR_046350.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs36223 5:64865975 T ENSESTG00000013010 ENSESTT00000032643 Transcript downstream_gene_variant - - - - - - DISTANCE=224 rs36223 5:64865975 T ENSESTG00000013010 ENSESTT00000032640 Transcript intron_variant - - - - - - rs259056 5:65410583 C - - - intergenic_variant - - - - - - rs4616843 5:65529695 G ENSESTG00000011824 ENSESTT00000029645 Transcript intron_variant - - - - - - rs6414803 5:65588399 C ENSESTG00000011824 ENSESTT00000029645 Transcript intron_variant - - - - - - rs12659820 5:65861154 G - - - intergenic_variant - - - - - - rs37548 5:66232592 C CCDS47224.1 CCDS47224.1 Transcript intron_variant - - - - - - rs37548 5:66232592 C CCDS54861.1 CCDS54861.1 Transcript intron_variant - - - - - - rs37548 5:66232592 C 375449 NM_198828.2 Transcript intron_variant - - - - - - rs37548 5:66232592 C ENSESTG00000006465 ENSESTT00000016300 Transcript intron_variant - - - - - - rs37548 5:66232592 C ENSESTG00000006465 ENSESTT00000016312 Transcript intron_variant - - - - - - rs37548 5:66232592 C CCDS47225.1 CCDS47225.1 Transcript intron_variant - - - - - - rs37548 5:66232592 C ENSESTG00000006465 ENSESTT00000016323 Transcript intron_variant - - - - - - rs37548 5:66232592 C 375449 NM_001164664.1 Transcript intron_variant - - - - - - rs37548 5:66232592 C 375449 NM_015183.2 Transcript intron_variant - - - - - - rs27396 5:66243272 T CCDS47224.1 CCDS47224.1 Transcript intron_variant - - - - - - rs27396 5:66243272 T CCDS54861.1 CCDS54861.1 Transcript intron_variant - - - - - - rs27396 5:66243272 T 375449 NM_198828.2 Transcript intron_variant - - - - - - rs27396 5:66243272 T ENSESTG00000006465 ENSESTT00000016300 Transcript intron_variant - - - - - - rs27396 5:66243272 T ENSESTG00000006465 ENSESTT00000016312 Transcript intron_variant - - - - - - rs27396 5:66243272 T CCDS47225.1 CCDS47225.1 Transcript intron_variant - - - - - - rs27396 5:66243272 T ENSESTG00000006465 ENSESTT00000016323 Transcript intron_variant - - - - - - rs27396 5:66243272 T 375449 NM_001164664.1 Transcript intron_variant - - - - - - rs27396 5:66243272 T 375449 NM_015183.2 Transcript intron_variant - - - - - - rs1295188 5:66351030 G ENSESTG00000006465 ENSESTT00000016354 Transcript intron_variant - - - - - - rs1295188 5:66351030 G CCDS54861.1 CCDS54861.1 Transcript intron_variant - - - - - - rs1295188 5:66351030 G ENSESTG00000006465 ENSESTT00000016334 Transcript intron_variant - - - - - - rs1295188 5:66351030 G ENSESTG00000006465 ENSESTT00000016351 Transcript intron_variant - - - - - - rs1295188 5:66351030 G ENSESTG00000006465 ENSESTT00000016337 Transcript intron_variant - - - - - - rs1295188 5:66351030 G CCDS47225.1 CCDS47225.1 Transcript intron_variant - - - - - - rs1295188 5:66351030 G 375449 NM_001164664.1 Transcript intron_variant - - - - - - rs1295188 5:66351030 G 375449 NM_015183.2 Transcript intron_variant - - - - - - rs6449856 5:66611217 C - ENSR00001410154 RegulatoryFeature regulatory_region_variant - - - - - - rs6449856 5:66611217 C - - - intergenic_variant - - - - - - rs32014 5:66649701 C - - - intergenic_variant - - - - - - rs429114 5:66692169 T - - - intergenic_variant - - - - - - rs32040 5:66732048 C - - - intergenic_variant - - - - - - rs281464 5:67331910 C - - - intergenic_variant - - - - - - rs40502 5:67628272 T - ENSR00001282174 RegulatoryFeature regulatory_region_variant - - - - - - rs40502 5:67628272 T ENSESTG00000006644 ENSESTT00000016802 Transcript intron_variant - - - - - - rs1651514 5:68002236 G - - - intergenic_variant - - - - - - rs1650758 5:68427564 T 64924 NM_022902.4 Transcript downstream_gene_variant - - - - - - DISTANCE=665 rs1650758 5:68427564 T ENSESTG00000035610 ENSESTT00000089953 Transcript downstream_gene_variant - - - - - - DISTANCE=1866 rs1650758 5:68427564 T ENSESTG00000035610 ENSESTT00000089949 Transcript downstream_gene_variant - - - - - - DISTANCE=1866 rs1650758 5:68427564 T ENSESTG00000035666 ENSESTT00000090099 Transcript intron_variant - - - - - - rs1650758 5:68427564 T ENSESTG00000035610 ENSESTT00000089956 Transcript downstream_gene_variant - - - - - - DISTANCE=1866 rs1650758 5:68427564 T CCDS3996.1 CCDS3996.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2120 rs7444232 5:70932170 T ENSESTG00000017258 ENSESTT00000043557 Transcript intron_variant - - - - - - rs7444232 5:70932170 T 64087 NM_022132.4 Transcript intron_variant - - - - - - rs7444232 5:70932170 T ENSESTG00000017258 ENSESTT00000043532 Transcript intron_variant - - - - - - rs7444232 5:70932170 T CCDS34184.1 CCDS34184.1 Transcript intron_variant - - - - - - rs7444232 5:70932170 T ENSESTG00000017258 ENSESTT00000043569 Transcript intron_variant - - - - - - rs7444232 5:70932170 T ENSESTG00000017258 ENSESTT00000043525 Transcript intron_variant - - - - - - rs7443853 5:70982845 T - - - intergenic_variant - - - - - - rs6887005 5:71018606 G ENSESTG00000016256 ENSESTT00000040824 Transcript downstream_gene_variant - - - - - - DISTANCE=1838 rs6887005 5:71018606 G CCDS4011.1 CCDS4011.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2164 rs6887005 5:71018606 G 9607 NM_004291.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1731 rs6887005 5:71018606 G ENSESTG00000016256 ENSESTT00000040829 Transcript downstream_gene_variant - - - - - - DISTANCE=2039 rs3010272 5:72049704 C - - - intergenic_variant - - - - - - rs56851308 5:72126362 C ENSESTG00000025821 ENSESTT00000065531 Transcript intron_variant - - - - - - rs56851308 5:72126362 C ENSESTG00000025821 ENSESTT00000065547 Transcript intron_variant - - - - - - rs56851308 5:72126362 C ENSESTG00000025821 ENSESTT00000065090 Transcript intron_variant - - - - - - rs56851308 5:72126362 C ENSESTG00000025821 ENSESTT00000065575 Transcript intron_variant - - - - - - rs56851308 5:72126362 C CCDS43329.1 CCDS43329.1 Transcript intron_variant - - - - - - rs56851308 5:72126362 C 3842 NM_002270.3 Transcript intron_variant - - - - - - rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065531 Transcript intron_variant - - - - - - rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065547 Transcript intron_variant - - - - - - rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065575 Transcript downstream_gene_variant - - - - - - DISTANCE=3279 rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065654 Transcript intron_variant - - - - - - rs250516 5:72200180 A 3842 NM_002270.3 Transcript intron_variant - - - - - - rs250516 5:72200180 A CCDS4016.1 CCDS4016.1 Transcript intron_variant - - - - - - rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065662 Transcript downstream_gene_variant - - - - - - DISTANCE=3279 rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065677 Transcript intron_variant - - - - - - rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065612 Transcript intron_variant - - - - - - rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065679 Transcript downstream_gene_variant - - - - - - DISTANCE=3279 rs250516 5:72200180 A CCDS43329.1 CCDS43329.1 Transcript intron_variant - - - - - - rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065627 Transcript downstream_gene_variant - - - - - - DISTANCE=3279 rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065673 Transcript intron_variant - - - - - - rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065616 Transcript intron_variant - - - - - - rs250516 5:72200180 A 3842 NM_153188.2 Transcript intron_variant - - - - - - rs250516 5:72200180 A ENSESTG00000025821 ENSESTT00000065646 Transcript intron_variant - - - - - - rs7731777 5:72419410 G - ENSR00001282593 RegulatoryFeature regulatory_region_variant - - - - - - rs7731777 5:72419410 G 134285 NM_173490.6 Transcript synonymous_variant 414 210 70 G ggA/ggG - rs7731777 5:72419410 G 134285 NM_001161342.1 Transcript synonymous_variant 414 210 70 G ggA/ggG - rs7731777 5:72419410 G ENSESTG00000026209 ENSESTT00000066105 Transcript synonymous_variant 687 210 70 G ggA/ggG - rs7731777 5:72419410 G CCDS54869.1 CCDS54869.1 Transcript synonymous_variant 210 210 70 G ggA/ggG - rs7731777 5:72419410 G CCDS4017.1 CCDS4017.1 Transcript synonymous_variant 210 210 70 G ggA/ggG - rs7731777 5:72419410 G ENSESTG00000026209 ENSESTT00000066121 Transcript synonymous_variant 687 210 70 G ggA/ggG - rs2962280 5:73131745 G CCDS58957.1 CCDS58957.1 Transcript intron_variant - - - - - - rs2962280 5:73131745 G ENSESTG00000016800 ENSESTT00000042244 Transcript intron_variant - - - - - - rs2962280 5:73131745 G 64283 NM_001177693.1 Transcript intron_variant - - - - - - rs2962280 5:73131745 G 64283 NM_001080479.2 Transcript intron_variant - - - - - - rs2962280 5:73131745 G CCDS47231.2 CCDS47231.2 Transcript intron_variant - - - - - - rs2962280 5:73131745 G ENSESTG00000016800 ENSESTT00000042204 Transcript intron_variant - - - - - - rs2962280 5:73131745 G CCDS54870.1 CCDS54870.1 Transcript intron_variant - - - - - - rs2962280 5:73131745 G 64283 NM_001244364.1 Transcript intron_variant - - - - - - rs2931422 5:73163861 T CCDS58957.1 CCDS58957.1 Transcript intron_variant - - - - - - rs2931422 5:73163861 T ENSESTG00000016800 ENSESTT00000042244 Transcript downstream_gene_variant - - - - - - DISTANCE=2050 rs2931422 5:73163861 T 64283 NM_001177693.1 Transcript intron_variant - - - - - - rs2931422 5:73163861 T 64283 NM_001080479.2 Transcript intron_variant - - - - - - rs2931422 5:73163861 T CCDS47231.2 CCDS47231.2 Transcript intron_variant - - - - - - rs2931422 5:73163861 T ENSESTG00000016800 ENSESTT00000042204 Transcript downstream_gene_variant - - - - - - DISTANCE=2050 rs2931422 5:73163861 T CCDS54870.1 CCDS54870.1 Transcript intron_variant - - - - - - rs2931422 5:73163861 T 64283 NM_001244364.1 Transcript intron_variant - - - - - - rs2931422 5:73163861 T ENSESTG00000016826 ENSESTT00000042265 Transcript upstream_gene_variant - - - - - - DISTANCE=65 rs2973539 5:73282338 A - - - intergenic_variant - - - - - - rs298398 5:73826303 T - ENSR00001282921 RegulatoryFeature regulatory_region_variant - - - - - - rs298398 5:73826303 T ENSESTG00000016952 ENSESTT00000042508 Transcript intron_variant - - - - - - rs820845 5:73967909 C ENSESTG00000016915 ENSESTT00000042450 Transcript intron_variant - - - - - - rs6875035 5:74404558 A - ENSR00001410779 RegulatoryFeature regulatory_region_variant - - - - - - rs6875035 5:74404558 A 256006 NM_001164443.1 Transcript intron_variant - - - - - - rs6875035 5:74404558 A ENSESTG00000008416 ENSESTT00000021227 Transcript upstream_gene_variant - - - - - - DISTANCE=4389 rs1300858 5:74536893 G 256006 NM_001164443.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4190 rs1300858 5:74536893 G ENSESTG00000008407 ENSESTT00000021200 Transcript upstream_gene_variant - - - - - - DISTANCE=4190 rs34346 5:74937139 G ENSESTG00000008326 ENSESTT00000021010 Transcript intron_variant - - - - - - rs34346 5:74937139 G ENSESTG00000008326 ENSESTT00000021007 Transcript intron_variant - - - - - - rs34346 5:74937139 G 728780 XM_001128459.5 Transcript intron_variant - - - - - - rs6898717 5:75435069 C 22987 NM_014979.1 Transcript intron_variant - - - - - - rs6898717 5:75435069 C CCDS43331.1 CCDS43331.1 Transcript intron_variant - - - - - - rs4133658 5:76621612 T CCDS34190.1 CCDS34190.1 Transcript intron_variant - - - - - - rs4133658 5:76621612 T CCDS34192.1 CCDS34192.1 Transcript intron_variant - - - - - - rs4133658 5:76621612 T 8622 NM_003719.3 Transcript intron_variant - - - - - - rs4133658 5:76621612 T 8622 NM_001029853.2 Transcript intron_variant - - - - - - rs4133658 5:76621612 T 8622 NM_001029851.2 Transcript intron_variant - - - - - - rs4133658 5:76621612 T CCDS4037.1 CCDS4037.1 Transcript intron_variant - - - - - - rs4133658 5:76621612 T ENSESTG00000000226 ENSESTT00000000574 Transcript intron_variant - - - - - - rs4133658 5:76621612 T CCDS34191.1 CCDS34191.1 Transcript intron_variant - - - - - - rs4133658 5:76621612 T ENSESTG00000000226 ENSESTT00000000578 Transcript intron_variant - - - - - - rs4133658 5:76621612 T ENSESTG00000000226 ENSESTT00000000580 Transcript intron_variant - - - - - - rs4133658 5:76621612 T 8622 NM_001029852.2 Transcript intron_variant - - - - - - rs4133658 5:76621612 T 8622 NM_001029854.2 Transcript intron_variant - - - - - - rs4133658 5:76621612 T CCDS34193.1 CCDS34193.1 Transcript intron_variant - - - - - - rs4704406 5:76628992 C CCDS34190.1 CCDS34190.1 Transcript intron_variant - - - - - - rs4704406 5:76628992 C CCDS34192.1 CCDS34192.1 Transcript intron_variant - - - - - - rs4704406 5:76628992 C 8622 NM_003719.3 Transcript intron_variant - - - - - - rs4704406 5:76628992 C 8622 NM_001029853.2 Transcript intron_variant - - - - - - rs4704406 5:76628992 C 8622 NM_001029851.2 Transcript intron_variant - - - - - - rs4704406 5:76628992 C CCDS4037.1 CCDS4037.1 Transcript intron_variant - - - - - - rs4704406 5:76628992 C ENSESTG00000000226 ENSESTT00000000574 Transcript intron_variant - - - - - - rs4704406 5:76628992 C CCDS34191.1 CCDS34191.1 Transcript intron_variant - - - - - - rs4704406 5:76628992 C ENSESTG00000000226 ENSESTT00000000578 Transcript intron_variant - - - - - - rs4704406 5:76628992 C ENSESTG00000000226 ENSESTT00000000580 Transcript intron_variant - - - - - - rs4704406 5:76628992 C 8622 NM_001029852.2 Transcript intron_variant - - - - - - rs4704406 5:76628992 C 8622 NM_001029854.2 Transcript intron_variant - - - - - - rs4704406 5:76628992 C CCDS34193.1 CCDS34193.1 Transcript intron_variant - - - - - - rs335619 5:76687661 A CCDS34190.1 CCDS34190.1 Transcript intron_variant - - - - - - rs335619 5:76687661 A CCDS34192.1 CCDS34192.1 Transcript intron_variant - - - - - - rs335619 5:76687661 A 8622 NM_003719.3 Transcript intron_variant - - - - - - rs335619 5:76687661 A 8622 NM_001029853.2 Transcript intron_variant - - - - - - rs335619 5:76687661 A 8622 NM_001029851.2 Transcript intron_variant - - - - - - rs335619 5:76687661 A CCDS4037.1 CCDS4037.1 Transcript intron_variant - - - - - - rs335619 5:76687661 A ENSESTG00000000226 ENSESTT00000000574 Transcript intron_variant - - - - - - rs335619 5:76687661 A CCDS34191.1 CCDS34191.1 Transcript intron_variant - - - - - - rs335619 5:76687661 A ENSESTG00000000226 ENSESTT00000000581 Transcript intron_variant - - - - - - rs335619 5:76687661 A ENSESTG00000000226 ENSESTT00000000578 Transcript intron_variant - - - - - - rs335619 5:76687661 A ENSESTG00000000226 ENSESTT00000000580 Transcript intron_variant - - - - - - rs335619 5:76687661 A 8622 NM_001029852.2 Transcript intron_variant - - - - - - rs335619 5:76687661 A 8622 NM_001029854.2 Transcript intron_variant - - - - - - rs335619 5:76687661 A CCDS34193.1 CCDS34193.1 Transcript intron_variant - - - - - - rs186753 5:76704849 C ENSESTG00000000226 ENSESTT00000000583 Transcript synonymous_variant 335 177 59 P ccT/ccC - rs186753 5:76704849 C 8622 NM_001029853.2 Transcript synonymous_variant 1482 1437 479 P ccT/ccC - rs186753 5:76704849 C 8622 NM_001029851.2 Transcript synonymous_variant 1251 1206 402 P ccT/ccC - rs186753 5:76704849 C ENSESTG00000000226 ENSESTT00000000578 Transcript synonymous_variant 1598 783 261 P ccT/ccC - rs186753 5:76704849 C CCDS34193.1 CCDS34193.1 Transcript synonymous_variant 1437 1437 479 P ccT/ccC - rs186753 5:76704849 C CCDS34190.1 CCDS34190.1 Transcript intron_variant - - - - - - rs186753 5:76704849 C CCDS34192.1 CCDS34192.1 Transcript synonymous_variant 1206 1206 402 P ccT/ccC - rs186753 5:76704849 C 8622 NM_003719.3 Transcript synonymous_variant 1542 1497 499 P ccT/ccC - rs186753 5:76704849 C ENSESTG00000000226 ENSESTT00000000584 Transcript upstream_gene_variant - - - - - - DISTANCE=3065 rs186753 5:76704849 C ENSESTG00000000226 ENSESTT00000000574 Transcript synonymous_variant 1367 1125 375 P ccT/ccC - rs186753 5:76704849 C CCDS4037.1 CCDS4037.1 Transcript synonymous_variant 1497 1497 499 P ccT/ccC - rs186753 5:76704849 C ENSESTG00000000226 ENSESTT00000000581 Transcript synonymous_variant 705 597 199 P ccT/ccC - rs186753 5:76704849 C CCDS34191.1 CCDS34191.1 Transcript synonymous_variant 1356 1356 452 P ccT/ccC - rs186753 5:76704849 C 8622 NM_001029852.2 Transcript intron_variant - - - - - - rs186753 5:76704849 C ENSESTG00000000226 ENSESTT00000000580 Transcript synonymous_variant 1324 1125 375 P ccT/ccC - rs186753 5:76704849 C 8622 NM_001029854.2 Transcript synonymous_variant 1401 1356 452 P ccT/ccC - rs6889888 5:77166940 A - - - intergenic_variant - - - - - - rs344649 5:77954518 A - - - intergenic_variant - - - - - - rs563177 5:78017552 C - - - intergenic_variant - - - - - - rs7720635 5:78022858 G - - - intergenic_variant - - - - - - rs337861 5:78199733 G - ENSR00001283742 RegulatoryFeature regulatory_region_variant - - - - - - rs337861 5:78199733 G 411 NM_198709.2 Transcript intron_variant - - - - - - rs337861 5:78199733 G ENSESTG00000017200 ENSESTT00000043243 Transcript intron_variant - - - - - - rs337861 5:78199733 G 411 NM_000046.3 Transcript intron_variant - - - - - - rs337861 5:78199733 G CCDS43334.1 CCDS43334.1 Transcript intron_variant - - - - - - rs337861 5:78199733 G CCDS4043.1 CCDS4043.1 Transcript intron_variant - - - - - - rs394636 5:78211898 T - ENSR00001283748 RegulatoryFeature regulatory_region_variant - - - - - - rs394636 5:78211898 T 411 NM_198709.2 Transcript intron_variant - - - - - - rs394636 5:78211898 T ENSESTG00000017200 ENSESTT00000043243 Transcript intron_variant - - - - - - rs394636 5:78211898 T 411 NM_000046.3 Transcript intron_variant - - - - - - rs394636 5:78211898 T CCDS43334.1 CCDS43334.1 Transcript intron_variant - - - - - - rs394636 5:78211898 T CCDS4043.1 CCDS4043.1 Transcript intron_variant - - - - - - rs259104 5:79095991 A 202333 NM_153610.3 Transcript 3_prime_UTR_variant 12834 - - - - - rs259104 5:79095991 A ENSESTG00000018551 ENSESTT00000046858 Transcript 3_prime_UTR_variant 3345 - - - - - rs259104 5:79095991 A CCDS47238.1 CCDS47238.1 Transcript downstream_gene_variant - - - - - - DISTANCE=552 rs413411 5:79429330 C ENSESTG00000018778 ENSESTT00000047309 Transcript intron_variant - - - - - - rs413411 5:79429330 C CCDS54873.1 CCDS54873.1 Transcript intron_variant - - - - - - rs413411 5:79429330 C 256987 NM_001174071.1 Transcript intron_variant - - - - - - rs413411 5:79429330 C 256987 NM_178276.5 Transcript intron_variant - - - - - - rs259049 5:79701886 T 9765 NM_014733.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1952 rs259049 5:79701886 T 9765 NM_001105251.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1952 rs259049 5:79701886 T ENSESTG00000018790 ENSESTT00000047355 Transcript upstream_gene_variant - - - - - - DISTANCE=1973 rs259049 5:79701886 T ENSESTG00000018790 ENSESTT00000047378 Transcript upstream_gene_variant - - - - - - DISTANCE=2048 rs259049 5:79701886 T ENSESTG00000018790 ENSESTT00000047336 Transcript upstream_gene_variant - - - - - - DISTANCE=1676 rs2544590 5:79704566 C - ENSR00001283974 RegulatoryFeature regulatory_region_variant - - - - - - rs2544590 5:79704566 C 9765 NM_014733.3 Transcript intron_variant - - - - - - rs2544590 5:79704566 C 9765 NM_001105251.1 Transcript intron_variant - - - - - - rs2544590 5:79704566 C ENSESTG00000018790 ENSESTT00000047355 Transcript intron_variant - - - - - - rs2544590 5:79704566 C ENSESTG00000018790 ENSESTT00000047378 Transcript intron_variant - - - - - - rs2544590 5:79704566 C ENSESTG00000018790 ENSESTT00000047336 Transcript intron_variant - - - - - - rs2431217 5:79830382 G 167555 NM_205548.2 Transcript intron_variant - - - - - - rs2431217 5:79830382 G ENSESTG00000018953 ENSESTT00000047714 Transcript intron_variant - - - - - - rs2431217 5:79830382 G ENSESTG00000018953 ENSESTT00000047725 Transcript intron_variant - - - - - - rs2431217 5:79830382 G CCDS4051.1 CCDS4051.1 Transcript intron_variant - - - - - - rs245018 5:80016329 T CCDS34195.1 CCDS34195.1 Transcript intron_variant - - - - - - rs245018 5:80016329 T 4437 NM_002439.4 Transcript intron_variant - - - - - - rs245018 5:80016329 T ENSESTG00000005772 ENSESTT00000014713 Transcript intron_variant - - - - - - rs245018 5:80016329 T ENSESTG00000005772 ENSESTT00000014687 Transcript intron_variant - - - - - - rs6860109 5:80768046 T ENSESTG00000005928 ENSESTT00000015041 Transcript intron_variant - - - - - - rs6860109 5:80768046 T CCDS58961.1 CCDS58961.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T 23635 NM_001256736.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T CCDS58963.1 CCDS58963.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T 23635 NM_001256734.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T CCDS58960.1 CCDS58960.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T 23635 NM_001256733.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T 23635 NM_001256735.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T 23635 NM_001256732.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T ENSESTG00000005928 ENSESTT00000015039 Transcript intron_variant - - - - - - rs6860109 5:80768046 T ENSESTG00000005928 ENSESTT00000015046 Transcript intron_variant - - - - - - rs6860109 5:80768046 T 23635 NM_012446.3 Transcript intron_variant - - - - - - rs6860109 5:80768046 T CCDS4056.1 CCDS4056.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T ENSESTG00000005928 ENSESTT00000015043 Transcript intron_variant - - - - - - rs6860109 5:80768046 T CCDS58962.1 CCDS58962.1 Transcript intron_variant - - - - - - rs6860109 5:80768046 T ENSESTG00000005928 ENSESTT00000015035 Transcript intron_variant - - - - - - rs680990 5:80925115 C ENSESTG00000005928 ENSESTT00000015041 Transcript intron_variant - - - - - - rs680990 5:80925115 C CCDS58961.1 CCDS58961.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C 23635 NM_001256736.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C CCDS58963.1 CCDS58963.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C 23635 NM_001256734.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C CCDS58960.1 CCDS58960.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C 23635 NM_001256733.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C 23635 NM_001256735.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C 23635 NM_001256732.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C ENSESTG00000005928 ENSESTT00000015039 Transcript intron_variant - - - - - - rs680990 5:80925115 C ENSESTG00000005928 ENSESTT00000015046 Transcript intron_variant - - - - - - rs680990 5:80925115 C 23635 NM_012446.3 Transcript intron_variant - - - - - - rs680990 5:80925115 C CCDS4056.1 CCDS4056.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C ENSESTG00000005928 ENSESTT00000015043 Transcript intron_variant - - - - - - rs680990 5:80925115 C CCDS58962.1 CCDS58962.1 Transcript intron_variant - - - - - - rs680990 5:80925115 C ENSESTG00000005928 ENSESTT00000015035 Transcript intron_variant - - - - - - rs4703864 5:81277787 G ENSESTG00000034590 ENSESTT00000087519 Transcript intron_variant - - - - - - rs4703864 5:81277787 G 83734 NM_001131028.1 Transcript intron_variant - - - - - - rs4703864 5:81277787 G 83734 NM_031482.4 Transcript intron_variant - - - - - - rs4703864 5:81277787 G ENSESTG00000034590 ENSESTT00000087504 Transcript intron_variant - - - - - - rs4703864 5:81277787 G ENSESTG00000034590 ENSESTT00000087510 Transcript intron_variant - - - - - - rs4703865 5:81284884 C ENSESTG00000034590 ENSESTT00000087519 Transcript downstream_gene_variant - - - - - - DISTANCE=1412 rs4703865 5:81284884 C 83734 NM_001131028.1 Transcript intron_variant - - - - - - rs4703865 5:81284884 C 83734 NM_031482.4 Transcript intron_variant - - - - - - rs4703865 5:81284884 C CCDS4057.1 CCDS4057.1 Transcript intron_variant - - - - - - rs4703865 5:81284884 C ENSESTG00000034590 ENSESTT00000087504 Transcript intron_variant - - - - - - rs4703865 5:81284884 C ENSESTG00000034590 ENSESTT00000087510 Transcript intron_variant - - - - - - rs11951769 5:81326609 C 83734 NM_001131028.1 Transcript intron_variant - - - - - - rs11951769 5:81326609 C 83734 NM_031482.4 Transcript intron_variant - - - - - - rs11951769 5:81326609 C CCDS4057.1 CCDS4057.1 Transcript intron_variant - - - - - - rs11951769 5:81326609 C ENSESTG00000034590 ENSESTT00000087504 Transcript intron_variant - - - - - - rs11951769 5:81326609 C ENSESTG00000034590 ENSESTT00000087510 Transcript intron_variant - - - - - - rs4470744 5:81452925 A - ENSR00001284227 RegulatoryFeature regulatory_region_variant - - - - - - rs4470744 5:81452925 A 83734 NM_001131028.1 Transcript intron_variant - - - - - - rs4470744 5:81452925 A 83734 NM_031482.4 Transcript intron_variant - - - - - - rs4470744 5:81452925 A CCDS4057.1 CCDS4057.1 Transcript intron_variant - - - - - - rs4470744 5:81452925 A ENSESTG00000034590 ENSESTT00000087504 Transcript intron_variant - - - - - - rs4470744 5:81452925 A ENSESTG00000034590 ENSESTT00000087525 Transcript intron_variant - - - - - - rs4470744 5:81452925 A ENSESTG00000034590 ENSESTT00000087510 Transcript intron_variant - - - - - - rs37564 5:82228160 T - - - intergenic_variant - - - - - - rs256802 5:82253375 A - - - intergenic_variant - - - - - - rs32877 5:82292596 C - - - intergenic_variant - - - - - - rs2909013 5:82972878 C CCDS4061.1 CCDS4061.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3536 rs2909013 5:82972878 C ENSESTG00000009242 ENSESTT00000023177 Transcript intron_variant - - - - - - rs2909013 5:82972878 C 1404 NM_001884.3 Transcript intron_variant - - - - - - rs4703969 5:83152919 C - - - intergenic_variant - - - - - - rs32612 5:83343143 T CCDS4062.1 CCDS4062.1 Transcript intron_variant - - - - - - rs32612 5:83343143 T 10085 NM_005711.3 Transcript intron_variant - - - - - - rs1532392 5:83926908 A - - - intergenic_variant - - - - - - rs6452573 5:83978072 A - - - intergenic_variant - - - - - - rs6452577 5:84026198 G - - - intergenic_variant - - - - - - rs10043858 5:84069105 G - - - intergenic_variant - - - - - - rs7447297 5:84082265 T - - - intergenic_variant - - - - - - rs7710075 5:85010403 G - - - intergenic_variant - - - - - - rs6890056 5:85283204 G - - - intergenic_variant - - - - - - rs4354079 5:85854196 G - - - intergenic_variant - - - - - - rs2410721 5:86001686 C - - - intergenic_variant - - - - - - rs10474255 5:86549324 C - - - intergenic_variant - - - - - - rs7735756 5:87740387 T - - - intergenic_variant - - - - - - rs247553 5:88695480 T - ENSR00001284922 RegulatoryFeature regulatory_region_variant - - - - - - rs247553 5:88695480 T ENSESTG00000033331 ENSESTT00000084174 Transcript intron_variant - - - - - - rs6452847 5:89010099 C - - - intergenic_variant - - - - - - rs4348244 5:89081479 C - - - intergenic_variant - - - - - - rs277052 5:89165734 T - - - intergenic_variant - - - - - - rs7714229 5:89512416 C ENSESTG00000028898 ENSESTT00000072750 Transcript intron_variant - - - - - - rs639607 5:89909003 G - ENSR00001285027 RegulatoryFeature regulatory_region_variant - - - - - - rs639607 5:89909003 G CCDS47246.1 CCDS47246.1 Transcript intron_variant - - - - - - rs639607 5:89909003 G 84059 NM_032119.3 Transcript intron_variant - - - - - - rs639607 5:89909003 G ENSESTG00000028770 ENSESTT00000072431 Transcript intron_variant - - - - - - rs639607 5:89909003 G ENSESTG00000028770 ENSESTT00000072412 Transcript intron_variant - - - - - - rs639607 5:89909003 G 84059 NR_003149.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2460180 5:90031869 A CCDS47246.1 CCDS47246.1 Transcript intron_variant - - - - - - rs2460180 5:90031869 A ENSESTG00000013452 ENSESTT00000033663 Transcript intron_variant - - - - - - rs2460180 5:90031869 A 84059 NM_032119.3 Transcript intron_variant - - - - - - rs2460180 5:90031869 A 84059 NR_003149.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4916837 5:90300039 A ENSESTG00000013476 ENSESTT00000033769 Transcript intron_variant - - - - - - rs4916837 5:90300039 A ENSESTG00000013476 ENSESTT00000033775 Transcript intron_variant - - - - - - rs4916837 5:90300039 A CCDS47246.1 CCDS47246.1 Transcript intron_variant - - - - - - rs4916837 5:90300039 A 84059 NM_032119.3 Transcript intron_variant - - - - - - rs4916837 5:90300039 A 84059 NR_003149.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7733445 5:90320098 G ENSESTG00000013476 ENSESTT00000033769 Transcript intron_variant - - - - - - rs7733445 5:90320098 G ENSESTG00000013476 ENSESTT00000033775 Transcript intron_variant - - - - - - rs7733445 5:90320098 G CCDS47246.1 CCDS47246.1 Transcript intron_variant - - - - - - rs7733445 5:90320098 G 84059 NM_032119.3 Transcript intron_variant - - - - - - rs7733445 5:90320098 G 84059 NR_003149.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2941884 5:90505599 G - - - intergenic_variant - - - - - - rs2973459 5:90531820 G - - - intergenic_variant - - - - - - rs1423218 5:90698942 T 100129716 NR_027435.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs332517 5:90845999 G - - - intergenic_variant - - - - - - rs4577729 5:90931403 C - - - intergenic_variant - - - - - - rs10035678 5:90934345 G - - - intergenic_variant - - - - - - rs2973833 5:91002341 A - - - intergenic_variant - - - - - - rs6452974 5:91189994 C - - - intergenic_variant - - - - - - rs1345785 5:91259315 G - - - intergenic_variant - - - - - - rs416753 5:91315757 C - - - intergenic_variant - - - - - - rs4574527 5:91719024 A ENSESTG00000003048 ENSESTT00000007599 Transcript intron_variant - - - - - - rs7447453 5:91926167 C ENSESTG00000003058 ENSESTT00000007612 Transcript intron_variant - - - - - - rs2644789 5:92374622 G ENSESTG00000015837 ENSESTT00000039679 Transcript intron_variant - - - - - - rs6557077 5:92658414 G - - - intergenic_variant - - - - - - rs249254 5:92789851 G 441094 NR_021491.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs249254 5:92789851 G ENSESTG00000015818 ENSESTT00000039658 Transcript intron_variant - - - - - - rs249254 5:92789851 G 441094 NR_015369.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs249254 5:92789851 G ENSESTG00000015818 ENSESTT00000039649 Transcript intron_variant - - - - - - rs308201 5:93751510 C 285600 NM_001145678.1 Transcript intron_variant - - - - - - rs306571 5:94027025 G ENSESTG00000009673 ENSESTT00000024228 Transcript upstream_gene_variant - - - - - - DISTANCE=862 rs306571 5:94027025 G ENSESTG00000009661 ENSESTT00000024212 Transcript downstream_gene_variant - - - - - - DISTANCE=2643 rs306571 5:94027025 G CCDS4071.2 CCDS4071.2 Transcript intron_variant - - - - - - rs306571 5:94027025 G 84250 NM_032290.3 Transcript intron_variant - - - - - - rs448328 5:94553935 G 79772 NM_024717.4 Transcript intron_variant - - - - - - rs448328 5:94553935 G CCDS34203.1 CCDS34203.1 Transcript intron_variant - - - - - - rs6878669 5:94772540 T ENSESTG00000009703 ENSESTT00000024326 Transcript missense_variant 38 34 12 P/S Cct/Tct - rs6878669 5:94772540 T 153643 NM_152548.2 Transcript missense_variant 869 823 275 P/S Cct/Tct - PolyPhen=benign;SIFT=tolerated rs6878669 5:94772540 T CCDS43341.1 CCDS43341.1 Transcript missense_variant 823 823 275 P/S Cct/Tct - PolyPhen=benign;SIFT=tolerated rs2432176 5:94773442 C ENSESTG00000009703 ENSESTT00000024326 Transcript intron_variant - - - - - - rs2432176 5:94773442 C 153643 NM_152548.2 Transcript intron_variant - - - - - - rs2432176 5:94773442 C CCDS43341.1 CCDS43341.1 Transcript intron_variant - - - - - - rs40099 5:95092339 G 22836 NM_014899.3 Transcript intron_variant - - - - - - rs40099 5:95092339 G ENSESTG00000009674 ENSESTT00000024294 Transcript intron_variant - - - - - - rs40099 5:95092339 G CCDS4077.1 CCDS4077.1 Transcript intron_variant - - - - - - rs40099 5:95092339 G ENSESTG00000009674 ENSESTT00000024282 Transcript intron_variant - - - - - - rs40099 5:95092339 G ENSESTG00000009786 ENSESTT00000024502 Transcript intron_variant - - - - - - rs154445 5:95246695 C ENSESTG00000009755 ENSESTT00000024437 Transcript intron_variant - - - - - - rs154445 5:95246695 C ENSESTG00000009715 ENSESTT00000024321 Transcript downstream_gene_variant - - - - - - DISTANCE=3758 rs154445 5:95246695 C 22936 NM_012081.5 Transcript intron_variant - - - - - - rs154445 5:95246695 C CCDS4080.1 CCDS4080.1 Transcript intron_variant - - - - - - rs154445 5:95246695 C ENSESTG00000009755 ENSESTT00000024444 Transcript intron_variant - - - - - - rs6556915 5:95656455 A - ENSR00001285875 RegulatoryFeature regulatory_region_variant - - - - - - rs6556915 5:95656455 A - - - intergenic_variant - - - - - - rs26480 5:96102074 A ENSESTG00000032951 ENSESTT00000083347 Transcript intron_variant - - - - - - rs26480 5:96102074 A 831 NM_001190442.1 Transcript intron_variant - - - - - - rs26480 5:96102074 A ENSESTG00000032682 ENSESTT00000082696 Transcript intron_variant - - - - - - rs26480 5:96102074 A 831 NR_033798.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs26480 5:96102074 A ENSESTG00000032951 ENSESTT00000083335 Transcript intron_variant - - - - - - rs26480 5:96102074 A 831 NM_173060.3 Transcript intron_variant - - - - - - rs26480 5:96102074 A CCDS54883.1 CCDS54883.1 Transcript intron_variant - - - - - - rs26480 5:96102074 A CCDS4085.1 CCDS4085.1 Transcript intron_variant - - - - - - rs26480 5:96102074 A 51752 NM_016442.3 Transcript intron_variant - - - - - - rs26480 5:96102074 A CCDS54882.1 CCDS54882.1 Transcript intron_variant - - - - - - rs26480 5:96102074 A CCDS4082.1 CCDS4082.1 Transcript intron_variant - - - - - - rs26480 5:96102074 A 831 NM_001042440.2 Transcript intron_variant - - - - - - rs26480 5:96102074 A ENSESTG00000032682 ENSESTT00000082715 Transcript intron_variant - - - - - - rs2927621 5:96178125 C ENSESTG00000032942 ENSESTT00000083249 Transcript intron_variant - - - - - - rs6556944 5:96302298 C 4012 NM_175920.3 Transcript intron_variant - - - - - - rs6556944 5:96302298 C CCDS4087.1 CCDS4087.1 Transcript intron_variant - - - - - - rs6556944 5:96302298 C 4012 NM_005575.2 Transcript intron_variant - - - - - - rs27304 5:96329857 T ENSESTG00000032867 ENSESTT00000083046 Transcript downstream_gene_variant - - - - - - DISTANCE=225 rs27304 5:96329857 T ENSESTG00000032875 ENSESTT00000083122 Transcript intron_variant - - - - - - rs27304 5:96329857 T ENSESTG00000032875 ENSESTT00000083112 Transcript intron_variant - - - - - - rs27304 5:96329857 T ENSESTG00000032875 ENSESTT00000083121 Transcript intron_variant - - - - - - rs27304 5:96329857 T ENSESTG00000032875 ENSESTT00000083132 Transcript intron_variant - - - - - - rs27304 5:96329857 T 4012 NM_175920.3 Transcript intron_variant - - - - - - rs27304 5:96329857 T CCDS43346.1 CCDS43346.1 Transcript intron_variant - - - - - - rs27304 5:96329857 T CCDS4087.1 CCDS4087.1 Transcript intron_variant - - - - - - rs27304 5:96329857 T 4012 NM_005575.2 Transcript intron_variant - - - - - - rs27304 5:96329857 T ENSESTG00000032875 ENSESTT00000083114 Transcript intron_variant - - - - - - rs30830 5:96392464 A - - - intergenic_variant - - - - - - rs6556956 5:96581232 G - - - intergenic_variant - - - - - - rs2453498 5:96606090 G - - - intergenic_variant - - - - - - rs10037025 5:96690101 G - - - intergenic_variant - - - - - - rs10075326 5:96709828 T - - - intergenic_variant - - - - - - rs4869349 5:96710377 G - - - intergenic_variant - - - - - - rs4440385 5:96716008 T - - - intergenic_variant - - - - - - rs291814 5:96719561 C - - - intergenic_variant - - - - - - rs291810 5:96728516 T - - - intergenic_variant - - - - - - rs291809 5:96728697 C - - - intergenic_variant - - - - - - rs4242237 5:96732379 A - - - intergenic_variant - - - - - - rs1601417 5:96733927 A - - - intergenic_variant - - - - - - rs291800 5:96742349 G - - - intergenic_variant - - - - - - rs291815 5:96749206 T - - - intergenic_variant - - - - - - rs291825 5:96755441 G - - - intergenic_variant - - - - - - rs291830 5:96764578 G - - - intergenic_variant - - - - - - rs1825530 5:96775495 T - - - intergenic_variant - - - - - - rs6859047 5:96781443 A - - - intergenic_variant - - - - - - rs1385584 5:96782294 A - - - intergenic_variant - - - - - - rs4869353 5:96783067 A - - - intergenic_variant - - - - - - rs1843332 5:96811116 G - - - intergenic_variant - - - - - - rs7701692 5:96942264 C ENSESTG00000032904 ENSESTT00000083144 Transcript intron_variant - - - - - - rs7703301 5:97246541 A - - - intergenic_variant - - - - - - rs181946 5:97354174 A - - - intergenic_variant - - - - - - rs7716652 5:97505579 G - - - intergenic_variant - - - - - - rs4509048 5:97516244 T - ENSR00001286149 RegulatoryFeature regulatory_region_variant - - - - - - rs4509048 5:97516244 T - - - intergenic_variant - - - - - - rs168657 5:97917900 G - - - intergenic_variant - - - - - - rs159968 5:97987862 G - - - intergenic_variant - - - - - - rs167830 5:98190220 C CCDS34204.1 CCDS34204.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1864 rs167830 5:98190220 C ENSESTG00000007426 ENSESTT00000018768 Transcript downstream_gene_variant - - - - - - DISTANCE=1859 rs167830 5:98190220 C ENSESTG00000007426 ENSESTT00000018758 Transcript downstream_gene_variant - - - - - - DISTANCE=1859 rs167830 5:98190220 C ENSESTG00000007426 ENSESTT00000018739 Transcript downstream_gene_variant - - - - - - DISTANCE=1859 rs167830 5:98190220 C ENSESTG00000007426 ENSESTT00000018778 Transcript downstream_gene_variant - - - - - - DISTANCE=1722 rs167830 5:98190220 C 1105 NM_001270.2 Transcript downstream_gene_variant - - - - - - DISTANCE=688 rs6861750 5:98673980 G - - - intergenic_variant - - - - - - rs6859396 5:98682122 A - - - intergenic_variant - - - - - - rs6421828 5:98731489 C - - - intergenic_variant - - - - - - rs6883233 5:99138386 T - - - intergenic_variant - - - - - - rs6594799 5:99180959 C - - - intergenic_variant - - - - - - rs11241408 5:99458856 C - - - intergenic_variant - - - - - - rs4365822 5:99492359 G - - - intergenic_variant - - - - - - rs1910682 5:99557660 T - - - intergenic_variant - - - - - - rs323571 5:99694251 C ENSESTG00000028244 ENSESTT00000071006 Transcript downstream_gene_variant - - - - - - DISTANCE=2030 rs2400247 5:100352448 A - - - intergenic_variant - - - - - - rs1993654 5:100642573 A - - - intergenic_variant - - - - - - rs4703173 5:101058143 A - - - intergenic_variant - - - - - - rs4317297 5:101745322 C 133482 NM_173488.3 Transcript intron_variant - - - - - - rs4317297 5:101745322 C CCDS34206.1 CCDS34206.1 Transcript intron_variant - - - - - - rs974028 5:101864924 T - - - intergenic_variant - - - - - - rs1605077 5:101904034 T - - - intergenic_variant - - - - - - rs154257 5:102380870 A - - - intergenic_variant - - - - - - rs257002 5:102391855 T - - - intergenic_variant - - - - - - rs2545405 5:102826270 C - - - intergenic_variant - - - - - - rs4394102 5:103350203 G - - - intergenic_variant - - - - - - rs1664611 5:103533547 T ENSESTG00000029479 ENSESTT00000074187 Transcript downstream_gene_variant - - - - - - DISTANCE=998 rs1734160 5:103533655 A ENSESTG00000029479 ENSESTT00000074187 Transcript downstream_gene_variant - - - - - - DISTANCE=1106 rs2591432 5:103603342 A - - - intergenic_variant - - - - - - rs33815 5:103976378 T ENSESTG00000008483 ENSESTT00000021367 Transcript intron_variant - - - - - - rs325494 5:103987340 G ENSESTG00000008483 ENSESTT00000021367 Transcript intron_variant - - - - - - rs1846997 5:104020804 C ENSESTG00000008483 ENSESTT00000021367 Transcript intron_variant - - - - - - rs588961 5:104474713 C - - - intergenic_variant - - - - - - rs158625 5:104547475 T - - - intergenic_variant - - - - - - rs10037059 5:104574136 A - - - intergenic_variant - - - - - - rs286729 5:105144818 G - - - intergenic_variant - - - - - - rs286714 5:105159244 A - - - intergenic_variant - - - - - - rs6596649 5:105169371 A - - - intergenic_variant - - - - - - rs7446220 5:105704113 A - - - intergenic_variant - - - - - - rs6891439 5:105814219 C - - - intergenic_variant - - - - - - rs6874703 5:105821147 A - - - intergenic_variant - - - - - - rs4245989 5:106355284 C - - - intergenic_variant - - - - - - rs963789 5:106565868 T - - - intergenic_variant - - - - - - rs27600 5:106938927 T 1946 NM_001962.2 Transcript intron_variant - - - - - - rs27600 5:106938927 T CCDS4097.1 CCDS4097.1 Transcript intron_variant - - - - - - rs1025492 5:107274702 T ENSESTG00000012188 ENSESTT00000030521 Transcript intron_variant - - - - - - rs1025492 5:107274702 T ENSESTG00000012188 ENSESTT00000030515 Transcript intron_variant - - - - - - rs1025492 5:107274702 T 64839 NM_001163315.2 Transcript intron_variant - - - - - - rs1025492 5:107274702 T ENSESTG00000012188 ENSESTT00000030508 Transcript intron_variant - - - - - - rs1025492 5:107274702 T CCDS54886.1 CCDS54886.1 Transcript intron_variant - - - - - - rs1025492 5:107274702 T ENSESTG00000012188 ENSESTT00000030523 Transcript intron_variant - - - - - - rs1025492 5:107274702 T ENSESTG00000012188 ENSESTT00000030495 Transcript intron_variant - - - - - - rs1549149 5:107833042 T - - - intergenic_variant - - - - - - rs6895422 5:108193956 C ENSESTG00000005470 ENSESTT00000013924 Transcript intron_variant - - - - - - rs6895422 5:108193956 C 2241 NM_005246.2 Transcript intron_variant - - - - - - rs6895422 5:108193956 C ENSESTG00000005470 ENSESTT00000013933 Transcript intron_variant - - - - - - rs6895422 5:108193956 C ENSESTG00000005470 ENSESTT00000013927 Transcript intron_variant - - - - - - rs6895422 5:108193956 C ENSESTG00000005470 ENSESTT00000013941 Transcript intron_variant - - - - - - rs6895422 5:108193956 C ENSESTG00000005470 ENSESTT00000013938 Transcript intron_variant - - - - - - rs6895422 5:108193956 C ENSESTG00000005470 ENSESTT00000013919 Transcript intron_variant - - - - - - rs6895422 5:108193956 C ENSESTG00000005470 ENSESTT00000013945 Transcript intron_variant - - - - - - rs6895422 5:108193956 C CCDS4098.1 CCDS4098.1 Transcript intron_variant - - - - - - rs6895422 5:108193956 C ENSESTG00000005470 ENSESTT00000013914 Transcript intron_variant - - - - - - rs11240988 5:108208597 C - ENSR00001412522 RegulatoryFeature regulatory_region_variant - - - - - - rs11240988 5:108208597 C ENSESTG00000005470 ENSESTT00000013924 Transcript intron_variant - - - - - - rs11240988 5:108208597 C 2241 NM_005246.2 Transcript intron_variant - - - - - - rs11240988 5:108208597 C ENSESTG00000005470 ENSESTT00000013933 Transcript intron_variant - - - - - - rs11240988 5:108208597 C ENSESTG00000005470 ENSESTT00000013927 Transcript intron_variant - - - - - - rs11240988 5:108208597 C ENSESTG00000005470 ENSESTT00000013941 Transcript intron_variant - - - - - - rs11240988 5:108208597 C ENSESTG00000005470 ENSESTT00000013938 Transcript intron_variant - - - - - - rs11240988 5:108208597 C ENSESTG00000005470 ENSESTT00000013919 Transcript intron_variant - - - - - - rs11240988 5:108208597 C ENSESTG00000005470 ENSESTT00000013945 Transcript intron_variant - - - - - - rs11240988 5:108208597 C CCDS4098.1 CCDS4098.1 Transcript intron_variant - - - - - - rs11240988 5:108208597 C ENSESTG00000005470 ENSESTT00000013914 Transcript intron_variant - - - - - - rs7446928 5:108899489 T - - - intergenic_variant - - - - - - rs248751 5:109071800 C 4124 NM_002372.2 Transcript intron_variant - - - - - - rs248751 5:109071800 C ENSESTG00000029190 ENSESTT00000073938 Transcript intron_variant - - - - - - rs248751 5:109071800 C ENSESTG00000029190 ENSESTT00000073922 Transcript intron_variant - - - - - - rs248751 5:109071800 C ENSESTG00000030307 ENSESTT00000076232 Transcript intron_variant - - - - - - rs248751 5:109071800 C CCDS34209.1 CCDS34209.1 Transcript intron_variant - - - - - - rs248751 5:109071800 C ENSESTG00000029190 ENSESTT00000073956 Transcript intron_variant - - - - - - rs245252 5:109316903 C - - - intergenic_variant - - - - - - rs245249 5:109318464 C - - - intergenic_variant - - - - - - rs36795 5:109327679 T - - - intergenic_variant - - - - - - rs36785 5:109334042 C - - - intergenic_variant - - - - - - rs2925103 5:109371841 A - - - intergenic_variant - - - - - - rs2925086 5:109398236 C - - - intergenic_variant - - - - - - rs2925083 5:109402232 A - - - intergenic_variant - - - - - - rs2966751 5:109412295 A - - - intergenic_variant - - - - - - rs4957586 5:109454834 G - - - intergenic_variant - - - - - - rs7711023 5:109483486 T - - - intergenic_variant - - - - - - rs4246004 5:109502190 G - - - intergenic_variant - - - - - - rs5001051 5:109622421 A ENSESTG00000029804 ENSESTT00000075241 Transcript intron_variant - - - - - - rs5001051 5:109622421 A ENSESTG00000030250 ENSESTT00000076105 Transcript downstream_gene_variant - - - - - - DISTANCE=2513 rs313608 5:109794982 T ENSESTG00000029804 ENSESTT00000075051 Transcript intron_variant - - - - - - rs313608 5:109794982 T CCDS47253.2 CCDS47253.2 Transcript intron_variant - - - - - - rs313608 5:109794982 T ENSESTG00000029804 ENSESTT00000075058 Transcript intron_variant - - - - - - rs313608 5:109794982 T 642987 NM_001039763.3 Transcript intron_variant - - - - - - rs13153189 5:109795081 T ENSESTG00000029804 ENSESTT00000075051 Transcript intron_variant - - - - - - rs13153189 5:109795081 T CCDS47253.2 CCDS47253.2 Transcript intron_variant - - - - - - rs13153189 5:109795081 T ENSESTG00000029804 ENSESTT00000075058 Transcript intron_variant - - - - - - rs13153189 5:109795081 T 642987 NM_001039763.3 Transcript intron_variant - - - - - - rs313623 5:109829274 A ENSESTG00000029804 ENSESTT00000075051 Transcript intron_variant - - - - - - rs313623 5:109829274 A CCDS47253.2 CCDS47253.2 Transcript intron_variant - - - - - - rs313623 5:109829274 A ENSESTG00000029804 ENSESTT00000075058 Transcript intron_variant - - - - - - rs313623 5:109829274 A 642987 NM_001039763.3 Transcript intron_variant - - - - - - rs313619 5:109861693 T ENSESTG00000029804 ENSESTT00000075051 Transcript intron_variant - - - - - - rs313619 5:109861693 T CCDS47253.2 CCDS47253.2 Transcript intron_variant - - - - - - rs313619 5:109861693 T ENSESTG00000029804 ENSESTT00000075080 Transcript downstream_gene_variant - - - - - - DISTANCE=2647 rs313619 5:109861693 T ENSESTG00000029804 ENSESTT00000075058 Transcript intron_variant - - - - - - rs313619 5:109861693 T 642987 NM_001039763.3 Transcript intron_variant - - - - - - rs7712781 5:111152904 T 9315 NM_001142475.1 Transcript intron_variant - - - - - - rs7712781 5:111152904 T CCDS47255.1 CCDS47255.1 Transcript intron_variant - - - - - - rs7712781 5:111152904 T 9315 NM_001142474.1 Transcript intron_variant - - - - - - rs4643999 5:111175198 A 9315 NM_001142475.1 Transcript intron_variant - - - - - - rs4643999 5:111175198 A CCDS47255.1 CCDS47255.1 Transcript intron_variant - - - - - - rs4643999 5:111175198 A 9315 NM_001142474.1 Transcript intron_variant - - - - - - rs6421835 5:111211860 T 9315 NM_001142475.1 Transcript intron_variant - - - - - - rs6421835 5:111211860 T CCDS47255.1 CCDS47255.1 Transcript intron_variant - - - - - - rs6421835 5:111211860 T 9315 NM_001142474.1 Transcript intron_variant - - - - - - rs40964 5:111426910 C - - - intergenic_variant - - - - - - rs4635973 5:111521536 C ENSESTG00000008127 ENSESTT00000020589 Transcript intron_variant - - - - - - rs4635973 5:111521536 C ENSESTG00000008127 ENSESTT00000020580 Transcript intron_variant - - - - - - rs4635973 5:111521536 C CCDS43350.1 CCDS43350.1 Transcript intron_variant - - - - - - rs4635973 5:111521536 C 64097 NM_022140.3 Transcript intron_variant - - - - - - rs186859 5:111775921 G - - - intergenic_variant - - - - - - rs33555 5:112312676 C - ENSR00001287655 RegulatoryFeature regulatory_region_variant - - - - - - rs33555 5:112312676 C 167227 NM_152624.5 Transcript missense_variant 270 46 16 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs33555 5:112312676 C 167227 NM_001242377.1 Transcript missense_variant 270 46 16 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs33555 5:112312676 C CCDS56377.1 CCDS56377.1 Transcript missense_variant 46 46 16 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs33555 5:112312676 C ENSESTG00000032550 ENSESTT00000082242 Transcript missense_variant 184 46 16 F/L Ttc/Ctc - rs33555 5:112312676 C 167227 NR_038352.1 Transcript non_coding_exon_variant,nc_transcript_variant 270 - - - - - rs33555 5:112312676 C ENSESTG00000032550 ENSESTT00000082251 Transcript 5_prime_UTR_variant 166 - - - - - rs33555 5:112312676 C ENSESTG00000032550 ENSESTT00000082229 Transcript missense_variant 184 46 16 F/L Ttc/Ctc - rs33555 5:112312676 C CCDS34210.1 CCDS34210.1 Transcript missense_variant 46 46 16 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs11241189 5:112338344 G - ENSR00001412844 RegulatoryFeature regulatory_region_variant - - - - - - rs11241189 5:112338344 G 167227 NM_152624.5 Transcript intron_variant - - - - - - rs11241189 5:112338344 G 167227 NM_001242377.1 Transcript intron_variant - - - - - - rs11241189 5:112338344 G CCDS56377.1 CCDS56377.1 Transcript intron_variant - - - - - - rs11241189 5:112338344 G ENSESTG00000032550 ENSESTT00000082242 Transcript intron_variant - - - - - - rs11241189 5:112338344 G 167227 NR_038352.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs11241189 5:112338344 G ENSESTG00000032550 ENSESTT00000082229 Transcript intron_variant - - - - - - rs11241189 5:112338344 G CCDS34210.1 CCDS34210.1 Transcript intron_variant - - - - - - rs10066096 5:112477989 C - ENSR00001412861 RegulatoryFeature regulatory_region_variant - - - - - - rs10066096 5:112477989 C ENSESTG00000032669 ENSESTT00000082530 Transcript intron_variant - - - - - - rs10066096 5:112477989 C ENSESTG00000032669 ENSESTT00000082518 Transcript intron_variant - - - - - - rs10066096 5:112477989 C 4163 NM_002387.2 Transcript intron_variant - - - - - - rs10066096 5:112477989 C ENSESTG00000032669 ENSESTT00000082558 Transcript intron_variant - - - - - - rs10066096 5:112477989 C 4163 NM_001085377.1 Transcript intron_variant - - - - - - rs10066096 5:112477989 C CCDS43351.1 CCDS43351.1 Transcript intron_variant - - - - - - rs10066096 5:112477989 C CCDS4111.1 CCDS4111.1 Transcript intron_variant - - - - - - rs7732247 5:112668144 C 4163 NM_001085377.1 Transcript intron_variant - - - - - - rs7732247 5:112668144 C CCDS43351.1 CCDS43351.1 Transcript intron_variant - - - - - - rs2972255 5:112816461 T 4163 NM_001085377.1 Transcript intron_variant - - - - - - rs2972255 5:112816461 T CCDS43351.1 CCDS43351.1 Transcript intron_variant - - - - - - rs4705569 5:113024917 T - - - intergenic_variant - - - - - - rs1482367 5:113072257 T - - - intergenic_variant - - - - - - rs6594764 5:113162953 A - - - intergenic_variant - - - - - - rs10045174 5:113499338 C - - - intergenic_variant - - - - - - rs4333303 5:113559291 C - - - intergenic_variant - - - - - - rs4298247 5:113581073 C - - - intergenic_variant - - - - - - rs2045588 5:113825832 A ENSESTG00000021349 ENSESTT00000053580 Transcript intron_variant - - - - - - rs2045588 5:113825832 A ENSESTG00000021349 ENSESTT00000053590 Transcript intron_variant - - - - - - rs2045588 5:113825832 A CCDS4114.1 CCDS4114.1 Transcript intron_variant - - - - - - rs2045588 5:113825832 A ENSESTG00000021323 ENSESTT00000053546 Transcript intron_variant - - - - - - rs2045588 5:113825832 A 3781 NM_021614.2 Transcript intron_variant - - - - - - rs2045588 5:113825832 A 3781 NM_170775.1 Transcript intron_variant - - - - - - rs2045588 5:113825832 A CCDS43352.1 CCDS43352.1 Transcript intron_variant - - - - - - rs287666 5:114017116 A ENSESTG00000021349 ENSESTT00000053580 Transcript intron_variant - - - - - - rs287683 5:114054654 G ENSESTG00000021349 ENSESTT00000053580 Transcript intron_variant - - - - - - rs2681514 5:114061934 C - ENSR00001412919 RegulatoryFeature regulatory_region_variant - - - - - - rs2681514 5:114061934 C ENSESTG00000021349 ENSESTT00000053580 Transcript intron_variant - - - - - - rs4585438 5:114213230 T - - - intergenic_variant - - - - - - rs4466153 5:114246423 G - - - intergenic_variant - - - - - - rs4291003 5:114275383 G - - - intergenic_variant - - - - - - rs2974510 5:114439936 G - - - intergenic_variant - - - - - - rs265404 5:114498393 A CCDS4115.1 CCDS4115.1 Transcript intron_variant - - - - - - rs265404 5:114498393 A ENSESTG00000030722 ENSESTT00000077337 Transcript intron_variant - - - - - - rs265404 5:114498393 A ENSESTG00000030722 ENSESTT00000077415 Transcript intron_variant - - - - - - rs265404 5:114498393 A ENSESTG00000030722 ENSESTT00000077389 Transcript intron_variant - - - - - - rs265404 5:114498393 A 55521 NM_018700.3 Transcript intron_variant - - - - - - rs265426 5:114556262 C 5229 NM_005023.3 Transcript intron_variant - - - - - - rs265426 5:114556262 C ENSESTG00000030672 ENSESTT00000077293 Transcript intron_variant - - - - - - rs265426 5:114556262 C CCDS4116.1 CCDS4116.1 Transcript intron_variant - - - - - - rs2605187 5:114733054 C ENSESTG00000030618 ENSESTT00000077085 Transcript intron_variant - - - - - - rs2168374 5:114739065 G ENSESTG00000030618 ENSESTT00000077085 Transcript intron_variant - - - - - - rs256990 5:114911581 A - ENSR00001287979 RegulatoryFeature regulatory_region_variant - - - - - - rs256990 5:114911581 A ENSESTG00000030589 ENSESTT00000077039 Transcript downstream_gene_variant - - - - - - DISTANCE=4931 rs256990 5:114911581 A ENSESTG00000030589 ENSESTT00000077013 Transcript downstream_gene_variant - - - - - - DISTANCE=4923 rs256990 5:114911581 A CCDS54887.1 CCDS54887.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4665 rs256990 5:114911581 A 353376 NM_021649.6 Transcript downstream_gene_variant - - - - - - DISTANCE=2758 rs256990 5:114911581 A 100302736 NM_001164468.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2758 rs256990 5:114911581 A ENSESTG00000030589 ENSESTT00000077022 Transcript downstream_gene_variant - - - - - - DISTANCE=4943 rs256990 5:114911581 A CCDS4119.1 CCDS4119.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4665 rs256990 5:114911581 A 100302736 NM_001164469.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2758 rs153072 5:115063008 C - - - intergenic_variant - - - - - - rs40323 5:115179630 T CCDS4122.2 CCDS4122.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2381 rs40323 5:115179630 T ENSESTG00000003192 ENSESTT00000007958 Transcript upstream_gene_variant - - - - - - DISTANCE=2391 rs40323 5:115179630 T 9140 NM_004707.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2082 rs40323 5:115179630 T 9140 NR_033362.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2082 rs40323 5:115179630 T ENSESTG00000003082 ENSESTT00000007690 Transcript intron_variant - - - - - - rs40323 5:115179630 T CCDS4123.1 CCDS4123.1 Transcript intron_variant - - - - - - rs40323 5:115179630 T 9140 NR_033363.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2082 rs40323 5:115179630 T 1176 NM_001284.2 Transcript intron_variant - - - - - - rs1204766 5:115260837 A - - - intergenic_variant - - - - - - rs4921051 5:115337942 T - ENSR00001288049 RegulatoryFeature regulatory_region_variant - - - - - - rs4921051 5:115337942 T ENSESTG00000003103 ENSESTT00000007717 Transcript upstream_gene_variant - - - - - - DISTANCE=588 rs4921051 5:115337942 T CCDS4124.1 CCDS4124.1 Transcript intron_variant - - - - - - rs4921051 5:115337942 T 206338 NM_173800.4 Transcript intron_variant - - - - - - rs4921051 5:115337942 T ENSESTG00000003103 ENSESTT00000007711 Transcript intron_variant - - - - - - rs4566828 5:115594505 G ENSESTG00000003125 ENSESTT00000007768 Transcript intron_variant - - - - - - rs4566828 5:115594505 G CCDS34215.1 CCDS34215.1 Transcript intron_variant - - - - - - rs4566828 5:115594505 G 51397 NM_016144.2 Transcript intron_variant - - - - - - rs34966 5:115813726 G ENSESTG00000003163 ENSESTT00000007903 Transcript upstream_gene_variant - - - - - - DISTANCE=145 rs34966 5:115813726 G ENSESTG00000003141 ENSESTT00000007804 Transcript intron_variant - - - - - - rs34966 5:115813726 G ENSESTG00000003163 ENSESTT00000007889 Transcript missense_variant 1691 1528 510 Y/H Tat/Cat - rs34966 5:115813726 G 57556 NM_020796.3 Transcript missense_variant 2261 1552 518 Y/H Tat/Cat - PolyPhen=benign;SIFT=tolerated rs34966 5:115813726 G ENSESTG00000003141 ENSESTT00000007799 Transcript intron_variant - - - - - - rs34966 5:115813726 G ENSESTG00000003163 ENSESTT00000007898 Transcript missense_variant 1020 769 257 Y/H Tat/Cat - rs34966 5:115813726 G ENSESTG00000003163 ENSESTT00000007895 Transcript missense_variant 1691 1528 510 Y/H Tat/Cat - rs34966 5:115813726 G ENSESTG00000003163 ENSESTT00000007899 Transcript missense_variant 1020 769 257 Y/H Tat/Cat - rs34966 5:115813726 G ENSESTG00000003163 ENSESTT00000007908 Transcript upstream_gene_variant - - - - - - DISTANCE=2425 rs34966 5:115813726 G ENSESTG00000003163 ENSESTT00000007901 Transcript upstream_gene_variant - - - - - - DISTANCE=102 rs34966 5:115813726 G CCDS47256.1 CCDS47256.1 Transcript missense_variant 1552 1552 518 Y/H Tat/Cat - PolyPhen=benign;SIFT=tolerated rs686798 5:115973875 G - - - intergenic_variant - - - - - - rs4351191 5:116415123 C - - - intergenic_variant - - - - - - rs4920960 5:116458056 T - - - intergenic_variant - - - - - - rs267088 5:116898107 G 728342 NR_046089.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7733867 5:117166777 G - - - intergenic_variant - - - - - - rs6895968 5:117516700 A - - - intergenic_variant - - - - - - rs7446864 5:117755739 T - - - intergenic_variant - - - - - - rs4243438 5:117816289 C - - - intergenic_variant - - - - - - rs2059952 5:117936670 C ENSESTG00000028019 ENSESTT00000070497 Transcript intron_variant - - - - - - rs644248 5:118098336 C ENSESTG00000013726 ENSESTT00000034268 Transcript intron_variant - - - - - - rs6595185 5:118691929 T - ENSR00001288365 RegulatoryFeature regulatory_region_variant - - - - - - rs6595185 5:118691929 T ENSESTG00000013453 ENSESTT00000033746 Transcript intron_variant - - - - - - rs6595185 5:118691929 T ENSESTG00000013453 ENSESTT00000033732 Transcript intron_variant - - - - - - rs6595185 5:118691929 T ENSESTG00000013691 ENSESTT00000034218 Transcript upstream_gene_variant - - - - - - DISTANCE=433 rs6595185 5:118691929 T 25816 NM_014350.2 Transcript intron_variant - - - - - - rs6595185 5:118691929 T 25816 NM_001077654.1 Transcript intron_variant - - - - - - rs6595185 5:118691929 T ENSESTG00000013453 ENSESTT00000033723 Transcript intron_variant - - - - - - rs6595185 5:118691929 T CCDS47258.1 CCDS47258.1 Transcript intron_variant - - - - - - rs6595185 5:118691929 T ENSESTG00000013686 ENSESTT00000034212 Transcript intron_variant - - - - - - rs6595185 5:118691929 T ENSESTG00000013453 ENSESTT00000033728 Transcript intron_variant - - - - - - rs6595185 5:118691929 T CCDS47257.1 CCDS47257.1 Transcript intron_variant - - - - - - rs2455465 5:118761479 A - - - intergenic_variant - - - - - - rs328665 5:118949122 A - - - intergenic_variant - - - - - - rs2973999 5:119180105 G - - - intergenic_variant - - - - - - rs7714355 5:119183121 G - - - intergenic_variant - - - - - - rs7704151 5:119485688 T - - - intergenic_variant - - - - - - rs4590202 5:119503785 T - - - intergenic_variant - - - - - - rs4895146 5:119508717 G - - - intergenic_variant - - - - - - rs4895147 5:119508969 G - - - intergenic_variant - - - - - - rs2124165 5:119821164 A CCDS4127.1 CCDS4127.1 Transcript intron_variant - - - - - - rs2124165 5:119821164 A 51334 NM_016644.1 Transcript intron_variant - - - - - - rs2124165 5:119821164 A ENSESTG00000004184 ENSESTT00000010539 Transcript intron_variant - - - - - - rs6899189 5:119828058 C CCDS4127.1 CCDS4127.1 Transcript intron_variant - - - - - - rs6899189 5:119828058 C 51334 NM_016644.1 Transcript intron_variant - - - - - - rs6899189 5:119828058 C ENSESTG00000004184 ENSESTT00000010539 Transcript intron_variant - - - - - - rs300960 5:119863423 A CCDS4127.1 CCDS4127.1 Transcript intron_variant - - - - - - rs300960 5:119863423 A 51334 NM_016644.1 Transcript intron_variant - - - - - - rs300960 5:119863423 A ENSESTG00000004184 ENSESTT00000010547 Transcript upstream_gene_variant - - - - - - DISTANCE=3736 rs300960 5:119863423 A ENSESTG00000004184 ENSESTT00000010539 Transcript intron_variant - - - - - - rs9327152 5:119931001 A CCDS4127.1 CCDS4127.1 Transcript intron_variant - - - - - - rs9327152 5:119931001 A 51334 NM_016644.1 Transcript intron_variant - - - - - - rs9327152 5:119931001 A ENSESTG00000004184 ENSESTT00000010547 Transcript intron_variant - - - - - - rs9327152 5:119931001 A ENSESTG00000004184 ENSESTT00000010539 Transcript intron_variant - - - - - - rs253699 5:120348033 A - - - intergenic_variant - - - - - - rs1422329 5:120613807 A - - - intergenic_variant - - - - - - rs7380074 5:121679235 T - ENSR00001288644 RegulatoryFeature regulatory_region_variant - - - - - - rs7380074 5:121679235 T 9627 NM_001242935.1 Transcript intron_variant - - - - - - rs7380074 5:121679235 T ENSESTG00000000339 ENSESTT00000000881 Transcript intron_variant - - - - - - rs7380074 5:121679235 T 9627 NM_005460.2 Transcript intron_variant - - - - - - rs7380074 5:121679235 T ENSESTG00000000339 ENSESTT00000000903 Transcript intron_variant - - - - - - rs7380074 5:121679235 T ENSESTG00000000339 ENSESTT00000000899 Transcript intron_variant - - - - - - rs7380074 5:121679235 T ENSESTG00000000339 ENSESTT00000000878 Transcript intron_variant - - - - - - rs7380074 5:121679235 T ENSESTG00000000339 ENSESTT00000000875 Transcript intron_variant - - - - - - rs7380074 5:121679235 T ENSESTG00000000339 ENSESTT00000000909 Transcript intron_variant - - - - - - rs7380074 5:121679235 T ENSESTG00000000339 ENSESTT00000000890 Transcript intron_variant - - - - - - rs7380074 5:121679235 T ENSESTG00000000339 ENSESTT00000000896 Transcript intron_variant - - - - - - rs7380074 5:121679235 T ENSESTG00000000339 ENSESTT00000000883 Transcript intron_variant - - - - - - rs9327257 5:121914399 A - - - intergenic_variant - - - - - - rs590780 5:122662990 C - - - intergenic_variant - - - - - - rs485847 5:122685801 A 153241 NM_153223.3 Transcript intron_variant - - - - - - rs485847 5:122685801 A CCDS54890.1 CCDS54890.1 Transcript intron_variant - - - - - - rs485847 5:122685801 A CCDS4134.2 CCDS4134.2 Transcript intron_variant - - - - - - rs485847 5:122685801 A 153241 NM_001166226.1 Transcript intron_variant - - - - - - rs485847 5:122685801 A ENSESTG00000031789 ENSESTT00000080287 Transcript intron_variant - - - - - - rs486812 5:122702220 T 153241 NM_153223.3 Transcript intron_variant - - - - - - rs486812 5:122702220 T CCDS54890.1 CCDS54890.1 Transcript intron_variant - - - - - - rs486812 5:122702220 T CCDS4134.2 CCDS4134.2 Transcript intron_variant - - - - - - rs486812 5:122702220 T 153241 NM_001166226.1 Transcript intron_variant - - - - - - rs486812 5:122702220 T ENSESTG00000031789 ENSESTT00000080287 Transcript intron_variant - - - - - - rs548948 5:122720395 C 153241 NM_153223.3 Transcript intron_variant - - - - - - rs548948 5:122720395 C CCDS54890.1 CCDS54890.1 Transcript intron_variant - - - - - - rs548948 5:122720395 C CCDS4134.2 CCDS4134.2 Transcript intron_variant - - - - - - rs548948 5:122720395 C 153241 NM_001166226.1 Transcript intron_variant - - - - - - rs548948 5:122720395 C ENSESTG00000031789 ENSESTT00000080287 Transcript upstream_gene_variant - - - - - - DISTANCE=2500 rs2546856 5:123272453 T - - - intergenic_variant - - - - - - rs330445 5:123279466 C - - - intergenic_variant - - - - - - rs2910232 5:123321793 T - - - intergenic_variant - - - - - - rs10037637 5:124317608 A - - - intergenic_variant - - - - - - rs1867517 5:124564000 T - - - intergenic_variant - - - - - - rs4836170 5:124633458 C - - - intergenic_variant - - - - - - rs1023798 5:124650768 C - - - intergenic_variant - - - - - - rs6875397 5:124651118 C - - - intergenic_variant - - - - - - rs4835869 5:124671709 G - - - intergenic_variant - - - - - - rs1826264 5:124767949 G - - - intergenic_variant - - - - - - rs9632455 5:124852510 C - - - intergenic_variant - - - - - - rs6898635 5:124861176 C - - - intergenic_variant - - - - - - rs6863788 5:125050774 T - - - intergenic_variant - - - - - - rs6595627 5:125051360 G - - - intergenic_variant - - - - - - rs570159 5:125355197 C - - - intergenic_variant - - - - - - rs443304 5:125637351 A - - - intergenic_variant - - - - - - rs4309971 5:125870278 G - - - intergenic_variant - - - - - - rs246891 5:126706819 T - ENSR00001413660 RegulatoryFeature regulatory_region_variant - - - - - - rs246891 5:126706819 T 84466 NM_001256545.1 Transcript intron_variant - - - - - - rs246891 5:126706819 T CCDS4142.1 CCDS4142.1 Transcript intron_variant - - - - - - rs246891 5:126706819 T 84466 NM_032446.2 Transcript intron_variant - - - - - - rs246891 5:126706819 T ENSESTG00000006309 ENSESTT00000015904 Transcript intron_variant - - - - - - rs246891 5:126706819 T ENSESTG00000006309 ENSESTT00000015915 Transcript downstream_gene_variant - - - - - - DISTANCE=1133 rs246891 5:126706819 T ENSESTG00000006309 ENSESTT00000015914 Transcript intron_variant - - - - - - rs2910217 5:126713040 T 84466 NM_001256545.1 Transcript intron_variant - - - - - - rs2910217 5:126713040 T CCDS4142.1 CCDS4142.1 Transcript intron_variant - - - - - - rs2910217 5:126713040 T 84466 NM_032446.2 Transcript intron_variant - - - - - - rs2910217 5:126713040 T ENSESTG00000006309 ENSESTT00000015904 Transcript intron_variant - - - - - - rs2910217 5:126713040 T ENSESTG00000006309 ENSESTT00000015914 Transcript intron_variant - - - - - - rs35421 5:126822934 A - - - intergenic_variant - - - - - - rs1356120 5:127141062 A - - - intergenic_variant - - - - - - rs711358 5:127161448 A - - - intergenic_variant - - - - - - rs247171 5:128029206 G - - - intergenic_variant - - - - - - rs247213 5:128115553 A - - - intergenic_variant - - - - - - rs1182083 5:128245988 G - - - intergenic_variant - - - - - - rs1181969 5:128353815 C CCDS4145.1 CCDS4145.1 Transcript intron_variant - - - - - - rs1181969 5:128353815 C 28965 NM_014031.3 Transcript intron_variant - - - - - - rs1181969 5:128353815 C 28965 NM_001017372.1 Transcript intron_variant - - - - - - rs1181969 5:128353815 C ENSESTG00000006232 ENSESTT00000015690 Transcript intron_variant - - - - - - rs1181969 5:128353815 C ENSESTG00000006228 ENSESTT00000015685 Transcript downstream_gene_variant - - - - - - DISTANCE=2143 rs2546795 5:128375161 A - - - intergenic_variant - - - - - - rs6595907 5:128763999 T - - - intergenic_variant - - - - - - rs33906 5:129220455 T ENSESTG00000003469 ENSESTT00000008643 Transcript intron_variant - - - - - - rs11950700 5:129365636 A 337876 NM_175856.4 Transcript intron_variant - - - - - - rs11950700 5:129365636 A ENSESTG00000003459 ENSESTT00000008635 Transcript intron_variant - - - - - - rs11950700 5:129365636 A CCDS34223.1 CCDS34223.1 Transcript intron_variant - - - - - - rs2863823 5:129483891 G 337876 NM_175856.4 Transcript intron_variant - - - - - - rs2863823 5:129483891 G ENSESTG00000003459 ENSESTT00000008635 Transcript intron_variant - - - - - - rs2863823 5:129483891 G CCDS34223.1 CCDS34223.1 Transcript intron_variant - - - - - - rs1016720 5:129623393 A - - - intergenic_variant - - - - - - rs2191107 5:129898041 G - - - intergenic_variant - - - - - - rs4705992 5:130313445 T - - - intergenic_variant - - - - - - rs43179 5:131038586 C 96459 NM_133372.2 Transcript intron_variant - - - - - - rs43179 5:131038586 C CCDS34226.1 CCDS34226.1 Transcript intron_variant - - - - - - rs43179 5:131038586 C CCDS34227.1 CCDS34227.1 Transcript intron_variant - - - - - - rs43179 5:131038586 C ENSESTG00000022416 ENSESTT00000056646 Transcript intron_variant - - - - - - rs43179 5:131038586 C 96459 NM_001008738.2 Transcript intron_variant - - - - - - rs1291671 5:131133043 C - ENSR00001413875 RegulatoryFeature regulatory_region_variant - - - - - - rs1291671 5:131133043 C 96459 NM_133372.2 Transcript upstream_gene_variant - - - - - - DISTANCE=287 rs1291671 5:131133043 C CCDS34226.1 CCDS34226.1 Transcript upstream_gene_variant - - - - - - DISTANCE=429 rs1291671 5:131133043 C ENSESTG00000022370 ENSESTT00000056562 Transcript upstream_gene_variant - - - - - - DISTANCE=244 rs1291671 5:131133043 C CCDS34227.1 CCDS34227.1 Transcript upstream_gene_variant - - - - - - DISTANCE=429 rs1291671 5:131133043 C 96459 NM_001008738.2 Transcript upstream_gene_variant - - - - - - DISTANCE=287 rs659490 5:131260338 T ENSESTG00000022308 ENSESTT00000056412 Transcript intron_variant - - - - - - rs659490 5:131260338 T 728637 XM_001131022.4 Transcript intron_variant - - - - - - rs659490 5:131260338 T ENSESTG00000022308 ENSESTT00000056406 Transcript intron_variant - - - - - - rs581231 5:131350399 G CCDS34229.1 CCDS34229.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3153 rs581231 5:131350399 G CCDS56383.1 CCDS56383.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2786 rs581231 5:131350399 G ENSESTG00000022210 ENSESTT00000056218 Transcript upstream_gene_variant - - - - - - DISTANCE=3069 rs581231 5:131350399 G ENSESTG00000022210 ENSESTT00000055984 Transcript upstream_gene_variant - - - - - - DISTANCE=2463 rs581231 5:131350399 G 23305 NM_001009185.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3044 rs581231 5:131350399 G 23305 NM_001205248.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2792 rs581231 5:131350399 G ENSESTG00000022210 ENSESTT00000056039 Transcript upstream_gene_variant - - - - - - DISTANCE=3035 rs581231 5:131350399 G 23305 NM_001205247.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3044 rs581231 5:131350399 G ENSESTG00000022210 ENSESTT00000056007 Transcript upstream_gene_variant - - - - - - DISTANCE=2638 rs581231 5:131350399 G CCDS34228.1 CCDS34228.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3153 rs581231 5:131350399 G ENSESTG00000022210 ENSESTT00000056016 Transcript upstream_gene_variant - - - - - - DISTANCE=2889 rs581231 5:131350399 G 23305 NM_015256.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3044 rs581231 5:131350399 G 23305 NM_001205250.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2638 rs581231 5:131350399 G 23305 NM_001205251.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2792 rs581231 5:131350399 G ENSESTG00000022210 ENSESTT00000056245 Transcript upstream_gene_variant - - - - - - DISTANCE=3069 rs40483 5:131434087 A - ENSR00001289972 RegulatoryFeature regulatory_region_variant - - - - - - rs40483 5:131434087 A - - - intergenic_variant - - - - - - rs157576 5:131594292 G - ENSR00001413911 RegulatoryFeature regulatory_region_variant - - - - - - rs157576 5:131594292 G CCDS4152.1 CCDS4152.1 Transcript intron_variant - - - - - - rs157576 5:131594292 G CCDS47261.1 CCDS47261.1 Transcript intron_variant - - - - - - rs157576 5:131594292 G ENSESTG00000021700 ENSESTT00000054498 Transcript intron_variant - - - - - - rs157576 5:131594292 G ENSESTG00000021700 ENSESTT00000054620 Transcript intron_variant - - - - - - rs157576 5:131594292 G 8572 NM_001131027.1 Transcript intron_variant - - - - - - rs157576 5:131594292 G 8572 NM_003687.3 Transcript intron_variant - - - - - - rs157576 5:131594292 G ENSESTG00000021700 ENSESTT00000054610 Transcript intron_variant - - - - - - rs157576 5:131594292 G ENSESTG00000022075 ENSESTT00000055699 Transcript intron_variant - - - - - - rs4551059 5:131719999 G ENSESTG00000021810 ENSESTT00000054946 Transcript splice_region_variant,intron_variant - - - - - - rs4551059 5:131719999 G CCDS4154.1 CCDS4154.1 Transcript splice_region_variant,intron_variant - - - - - - rs4551059 5:131719999 G ENSESTG00000021810 ENSESTT00000054932 Transcript splice_region_variant,intron_variant - - - - - - rs4551059 5:131719999 G ENSESTG00000021810 ENSESTT00000054954 Transcript upstream_gene_variant - - - - - - DISTANCE=4604 rs4551059 5:131719999 G 6584 NM_003060.3 Transcript splice_region_variant,intron_variant - - - - - - rs2706402 5:131882012 G CCDS4156.1 CCDS4156.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2842 rs2706402 5:131882012 G 3567 NM_000879.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2798 rs4705961 5:131952072 T 10111 NM_005732.3 Transcript intron_variant - - - - - - rs4705961 5:131952072 T ENSESTG00000033963 ENSESTT00000085882 Transcript intron_variant - - - - - - rs4705961 5:131952072 T ENSESTG00000033963 ENSESTT00000085878 Transcript intron_variant - - - - - - rs4705961 5:131952072 T CCDS34233.1 CCDS34233.1 Transcript intron_variant - - - - - - rs4705961 5:131952072 T ENSESTG00000033963 ENSESTT00000085886 Transcript intron_variant - - - - - - rs4705961 5:131952072 T ENSESTG00000022060 ENSESTT00000055558 Transcript intron_variant - - - - - - rs10055096 5:131970465 T ENSESTG00000034484 ENSESTT00000087223 Transcript downstream_gene_variant - - - - - - DISTANCE=3279 rs10055096 5:131970465 T 10111 NM_005732.3 Transcript intron_variant - - - - - - rs10055096 5:131970465 T ENSESTG00000033963 ENSESTT00000085882 Transcript intron_variant - - - - - - rs10055096 5:131970465 T ENSESTG00000033963 ENSESTT00000085878 Transcript intron_variant - - - - - - rs10055096 5:131970465 T ENSESTG00000034484 ENSESTT00000087217 Transcript downstream_gene_variant - - - - - - DISTANCE=3275 rs10055096 5:131970465 T CCDS34233.1 CCDS34233.1 Transcript intron_variant - - - - - - rs10055096 5:131970465 T ENSESTG00000022060 ENSESTT00000055558 Transcript intron_variant - - - - - - rs40470 5:132150948 G CCDS43361.1 CCDS43361.1 Transcript missense_variant 1635 1635 545 F/L ttT/ttG - PolyPhen=benign;SIFT=tolerated rs40470 5:132150948 G 134548 NM_175873.4 Transcript missense_variant 1916 1635 545 F/L ttT/ttG - PolyPhen=benign;SIFT=tolerated rs6895521 5:132399757 A ENSESTG00000034137 ENSESTT00000086396 Transcript intron_variant - - - - - - rs6895521 5:132399757 A CCDS4166.1 CCDS4166.1 Transcript intron_variant - - - - - - rs6895521 5:132399757 A 3308 NM_002154.3 Transcript intron_variant - - - - - - rs9327641 5:132467223 C - - - intergenic_variant - - - - - - rs890821 5:132534373 G ENSESTG00000034322 ENSESTT00000086812 Transcript downstream_gene_variant - - - - - - DISTANCE=789 rs890821 5:132534373 G CCDS34238.1 CCDS34238.1 Transcript downstream_gene_variant - - - - - - DISTANCE=414 rs890821 5:132534373 G 23105 NM_015082.1 Transcript 3_prime_UTR_variant 3161 - - - - - rs185416 5:133076273 T - - - intergenic_variant - - - - - - rs11242178 5:133086754 C - - - intergenic_variant - - - - - - rs11242179 5:133087806 C - - - intergenic_variant - - - - - - rs31234 5:133120853 C - - - intergenic_variant - - - - - - rs452715 5:133312966 G - ENSR00001414022 RegulatoryFeature regulatory_region_variant - - - - - - rs452715 5:133312966 G CCDS4168.1 CCDS4168.1 Transcript intron_variant - - - - - - rs452715 5:133312966 G 7416 NM_003374.2 Transcript intron_variant - - - - - - rs452715 5:133312966 G 7416 NR_036625.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs452715 5:133312966 G ENSESTG00000005009 ENSESTT00000012785 Transcript intron_variant - - - - - - rs452715 5:133312966 G ENSESTG00000005009 ENSESTT00000012789 Transcript intron_variant - - - - - - rs452715 5:133312966 G ENSESTG00000005009 ENSESTT00000012763 Transcript intron_variant - - - - - - rs452715 5:133312966 G ENSESTG00000005009 ENSESTT00000012782 Transcript intron_variant - - - - - - rs452715 5:133312966 G 7416 NR_036624.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs452715 5:133312966 G ENSESTG00000005009 ENSESTT00000012776 Transcript intron_variant - - - - - - rs258526 5:133821705 A ENSESTG00000004916 ENSESTT00000012499 Transcript intron_variant - - - - - - rs4958264 5:134009864 A ENSESTG00000017060 ENSESTT00000043008 Transcript upstream_gene_variant - - - - - - DISTANCE=910 rs4958264 5:134009864 A CCDS58967.1 CCDS58967.1 Transcript intron_variant - - - - - - rs4958264 5:134009864 A ENSESTG00000017060 ENSESTT00000042995 Transcript upstream_gene_variant - - - - - - DISTANCE=910 rs4958264 5:134009864 A ENSESTG00000017060 ENSESTT00000043016 Transcript upstream_gene_variant - - - - - - DISTANCE=910 rs4958264 5:134009864 A ENSESTG00000017060 ENSESTT00000043020 Transcript upstream_gene_variant - - - - - - DISTANCE=910 rs4958264 5:134009864 A CCDS43363.1 CCDS43363.1 Transcript intron_variant - - - - - - rs4958264 5:134009864 A 10802 NM_001252231.1 Transcript intron_variant - - - - - - rs4958264 5:134009864 A ENSESTG00000017060 ENSESTT00000043027 Transcript upstream_gene_variant - - - - - - DISTANCE=910 rs4958264 5:134009864 A ENSESTG00000017045 ENSESTT00000042842 Transcript intron_variant - - - - - - rs4958264 5:134009864 A 10802 NM_021982.2 Transcript intron_variant - - - - - - rs2548967 5:134163382 C ENSESTG00000017175 ENSESTT00000043538 Transcript intron_variant - - - - - - rs2548967 5:134163382 C ENSESTG00000017175 ENSESTT00000043495 Transcript intron_variant - - - - - - rs2548967 5:134163382 C ENSESTG00000017175 ENSESTT00000043426 Transcript intron_variant - - - - - - rs2548967 5:134163382 C 9879 NM_014829.2 Transcript intron_variant - - - - - - rs2548967 5:134163382 C ENSESTG00000017175 ENSESTT00000043352 Transcript intron_variant - - - - - - rs2548967 5:134163382 C CCDS34240.1 CCDS34240.1 Transcript intron_variant - - - - - - rs6596185 5:134197602 C 134553 NM_152409.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2177 rs6596185 5:134197602 C 134553 NM_001135586.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2177 rs2603004 5:134648592 A 100996485 XM_003846373.1 Transcript intron_variant - - - - - - rs9327717 5:134770010 G - ENSR00001290798 RegulatoryFeature regulatory_region_variant - - - - - - rs9327717 5:134770010 G - - - intergenic_variant - - - - - - rs245127 5:134881871 T - - - intergenic_variant - - - - - - rs5028740 5:135194054 G 153328 NM_145282.4 Transcript intron_variant - - - - - - rs5028740 5:135194054 G CCDS43366.2 CCDS43366.2 Transcript intron_variant - - - - - - rs5028740 5:135194054 G ENSESTG00000027815 ENSESTT00000070076 Transcript intron_variant - - - - - - rs5028740 5:135194054 G ENSESTG00000027815 ENSESTT00000070054 Transcript intron_variant - - - - - - rs5028740 5:135194054 G ENSESTG00000027815 ENSESTT00000070097 Transcript intron_variant - - - - - - rs31521 5:135286091 G CCDS4190.1 CCDS4190.1 Transcript intron_variant - - - - - - rs31521 5:135286091 G 3950 NM_002302.2 Transcript intron_variant - - - - - - rs31521 5:135286091 G ENSESTG00000028108 ENSESTT00000070713 Transcript intron_variant - - - - - - rs414936 5:136254139 T - - - intergenic_variant - - - - - - rs2961631 5:136570365 A ENSESTG00000022418 ENSESTT00000056655 Transcript intron_variant - - - - - - rs2961631 5:136570365 A CCDS4191.1 CCDS4191.1 Transcript intron_variant - - - - - - rs2961631 5:136570365 A 6695 NM_004598.3 Transcript intron_variant - - - - - - rs2961647 5:136607811 T ENSESTG00000022418 ENSESTT00000056655 Transcript intron_variant - - - - - - rs2961647 5:136607811 T ENSESTG00000022418 ENSESTT00000056606 Transcript intron_variant - - - - - - rs2961647 5:136607811 T CCDS4191.1 CCDS4191.1 Transcript intron_variant - - - - - - rs2961647 5:136607811 T 6695 NM_004598.3 Transcript intron_variant - - - - - - rs847823 5:137166591 G - - - intergenic_variant - - - - - - rs700609 5:137227987 A ENSESTG00000005002 ENSESTT00000012726 Transcript intron_variant - - - - - - rs700609 5:137227987 A ENSESTG00000004985 ENSESTT00000012696 Transcript downstream_gene_variant - - - - - - DISTANCE=4447 rs700609 5:137227987 A CCDS58971.1 CCDS58971.1 Transcript intron_variant - - - - - - rs700609 5:137227987 A 27039 NM_001258449.1 Transcript intron_variant - - - - - - rs700609 5:137227987 A 27039 NM_001258448.1 Transcript intron_variant - - - - - - rs700609 5:137227987 A CCDS4194.1 CCDS4194.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4913 rs700609 5:137227987 A 9499 NM_006790.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4447 rs700609 5:137227987 A 9499 NM_001135940.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4447 rs700609 5:137227987 A CCDS47268.1 CCDS47268.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4913 rs700609 5:137227987 A CCDS58972.1 CCDS58972.1 Transcript intron_variant - - - - - - rs700609 5:137227987 A 27039 NM_014386.3 Transcript intron_variant - - - - - - rs700609 5:137227987 A ENSESTG00000005002 ENSESTT00000012723 Transcript intron_variant - - - - - - rs700609 5:137227987 A CCDS43367.1 CCDS43367.1 Transcript intron_variant - - - - - - rs6874067 5:137258014 G - ENSR00001414326 RegulatoryFeature regulatory_region_variant - - - - - - rs6874067 5:137258014 G CCDS58971.1 CCDS58971.1 Transcript intron_variant - - - - - - rs6874067 5:137258014 G CCDS58972.1 CCDS58972.1 Transcript intron_variant - - - - - - rs6874067 5:137258014 G 27039 NM_014386.3 Transcript intron_variant - - - - - - rs6874067 5:137258014 G 27039 NM_001258449.1 Transcript intron_variant - - - - - - rs6874067 5:137258014 G 27039 NM_001258448.1 Transcript intron_variant - - - - - - rs6874067 5:137258014 G CCDS43367.1 CCDS43367.1 Transcript intron_variant - - - - - - rs11741193 5:137435577 C - - - intergenic_variant - - - - - - rs6596441 5:137930146 T - ENSR00001291325 RegulatoryFeature regulatory_region_variant - - - - - - rs6596441 5:137930146 T ENSESTG00000005184 ENSESTT00000013181 Transcript downstream_gene_variant - - - - - - DISTANCE=1075 rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000070066 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000070161 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000070112 Transcript intron_variant - - - - - - rs1508896 5:138142619 A 1495 NM_001903.2 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000069981 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000029344 ENSESTT00000073865 Transcript intron_variant - - - - - - rs1508896 5:138142619 A CCDS34243.1 CCDS34243.1 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000069950 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000070178 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000070121 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000070119 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000070165 Transcript intron_variant - - - - - - rs1508896 5:138142619 A ENSESTG00000027777 ENSESTT00000070044 Transcript intron_variant - - - - - - rs6864099 5:138292269 C ENSESTG00000029165 ENSESTT00000073694 Transcript intron_variant - - - - - - rs6864099 5:138292269 C 64374 NM_001037633.1 Transcript intron_variant - - - - - - rs6864099 5:138292269 C ENSESTG00000029165 ENSESTT00000073699 Transcript intron_variant - - - - - - rs6864099 5:138292269 C 64374 NM_022464.4 Transcript intron_variant - - - - - - rs6864099 5:138292269 C CCDS4209.1 CCDS4209.1 Transcript intron_variant - - - - - - rs6864099 5:138292269 C ENSESTG00000029165 ENSESTT00000073656 Transcript intron_variant - - - - - - rs6596474 5:138713959 C - ENSR00001291512 RegulatoryFeature regulatory_region_variant - - - - - - rs6596474 5:138713959 C CCDS4213.1 CCDS4213.1 Transcript missense_variant 1273 1273 425 S/A Tcc/Gcc - PolyPhen=benign;SIFT=tolerated rs6596474 5:138713959 C 9963 NM_152685.3 Transcript missense_variant 1370 1273 425 S/A Tcc/Gcc - PolyPhen=benign;SIFT=tolerated rs6596474 5:138713959 C CCDS4212.1 CCDS4212.1 Transcript missense_variant 1261 1261 421 S/A Tcc/Gcc - PolyPhen=benign;SIFT=tolerated rs6596474 5:138713959 C ENSESTG00000029118 ENSESTT00000073337 Transcript intron_variant - - - - - - rs6596474 5:138713959 C 9963 NM_005847.4 Transcript missense_variant 1358 1261 421 S/A Tcc/Gcc - PolyPhen=benign;SIFT=tolerated rs11242461 5:138718476 C CCDS4213.1 CCDS4213.1 Transcript intron_variant - - - - - - rs11242461 5:138718476 C 9963 NM_152685.3 Transcript intron_variant - - - - - - rs11242461 5:138718476 C CCDS4212.1 CCDS4212.1 Transcript intron_variant - - - - - - rs11242461 5:138718476 C 51237 NM_016459.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4781 rs11242461 5:138718476 C ENSESTG00000029118 ENSESTT00000073337 Transcript intron_variant - - - - - - rs11242461 5:138718476 C CCDS47273.1 CCDS47273.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4978 rs11242461 5:138718476 C 9963 NM_005847.4 Transcript intron_variant - - - - - - rs9327846 5:138724457 G - ENSR00001291522 RegulatoryFeature regulatory_region_variant - - - - - - rs9327846 5:138724457 G CCDS54909.1 CCDS54909.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3266 rs9327846 5:138724457 G 389333 NM_001161546.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3178 rs9327846 5:138724457 G 51237 NM_016459.3 Transcript intron_variant - - - - - - rs9327846 5:138724457 G CCDS47273.1 CCDS47273.1 Transcript intron_variant - - - - - - rs6596478 5:138731979 C - ENSR00001414422 RegulatoryFeature regulatory_region_variant - - - - - - rs6596478 5:138731979 C 202051 NM_194296.1 Transcript downstream_gene_variant - - - - - - DISTANCE=477 rs6596478 5:138731979 C ENSESTG00000028939 ENSESTT00000072892 Transcript downstream_gene_variant - - - - - - DISTANCE=496 rs6596478 5:138731979 C CCDS54909.1 CCDS54909.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1209 rs6596478 5:138731979 C CCDS47274.1 CCDS47274.1 Transcript downstream_gene_variant - - - - - - DISTANCE=510 rs6596478 5:138731979 C 389333 NM_001161546.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1094 rs6596478 5:138731979 C ENSESTG00000028939 ENSESTT00000072861 Transcript downstream_gene_variant - - - - - - DISTANCE=489 rs6865970 5:138733108 C 202051 NM_194296.1 Transcript intron_variant - - - - - - rs6865970 5:138733108 C ENSESTG00000028939 ENSESTT00000072892 Transcript intron_variant - - - - - - rs6865970 5:138733108 C CCDS54909.1 CCDS54909.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2338 rs6865970 5:138733108 C CCDS47274.1 CCDS47274.1 Transcript intron_variant - - - - - - rs6865970 5:138733108 C 389333 NM_001161546.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2223 rs6865970 5:138733108 C ENSESTG00000028939 ENSESTT00000072861 Transcript intron_variant - - - - - - rs7381176 5:138744315 T ENSESTG00000028607 ENSESTT00000071940 Transcript upstream_gene_variant - - - - - - DISTANCE=3935 rs7381176 5:138744315 T ENSESTG00000028813 ENSESTT00000072649 Transcript 3_prime_UTR_variant 1974 - - - - - rs7381176 5:138744315 T ENSESTG00000028813 ENSESTT00000072719 Transcript 3_prime_UTR_variant 1454 - - - - - rs7381176 5:138744315 T 202052 NM_152686.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1577 rs7381176 5:138744315 T ENSESTG00000028813 ENSESTT00000072799 Transcript 3_prime_UTR_variant 1261 - - - - - rs7381176 5:138744315 T 202051 NM_194296.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4539 rs7381176 5:138744315 T ENSESTG00000028813 ENSESTT00000072711 Transcript 3_prime_UTR_variant 1569 - - - - - rs7381176 5:138744315 T CCDS47274.1 CCDS47274.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4566 rs7381176 5:138744315 T ENSESTG00000028813 ENSESTT00000072667 Transcript 3_prime_UTR_variant 1859 - - - - - rs7381176 5:138744315 T ENSESTG00000028813 ENSESTT00000072791 Transcript 3_prime_UTR_variant 1376 - - - - - rs7381176 5:138744315 T ENSESTG00000028939 ENSESTT00000072861 Transcript upstream_gene_variant - - - - - - DISTANCE=4561 rs2649634 5:139121002 C - - - intergenic_variant - - - - - - rs6877284 5:139206654 C CCDS4216.1 CCDS4216.1 Transcript intron_variant - - - - - - rs6877284 5:139206654 C 84249 NM_032289.2 Transcript intron_variant - - - - - - rs4912884 5:139213452 G - ENSR00001414456 RegulatoryFeature regulatory_region_variant - - - - - - rs4912884 5:139213452 G CCDS4216.1 CCDS4216.1 Transcript intron_variant - - - - - - rs4912884 5:139213452 G ENSESTG00000010305 ENSESTT00000025756 Transcript upstream_gene_variant - - - - - - DISTANCE=4793 rs4912884 5:139213452 G 84249 NM_032289.2 Transcript intron_variant - - - - - - rs889019 5:139217957 T CCDS4216.1 CCDS4216.1 Transcript intron_variant - - - - - - rs889019 5:139217957 T ENSESTG00000010305 ENSESTT00000025756 Transcript upstream_gene_variant - - - - - - DISTANCE=288 rs889019 5:139217957 T 84249 NM_032289.2 Transcript intron_variant - - - - - - rs269765 5:139481281 C - - - intergenic_variant - - - - - - rs384532 5:140190589 T ENSESTG00000017796 ENSESTT00000044824 Transcript downstream_gene_variant - - - - - - DISTANCE=2552 rs384532 5:140190589 T 56147 NM_031411.1 Transcript intron_variant - - - - - - rs384532 5:140190589 T CCDS54914.1 CCDS54914.1 Transcript intron_variant - - - - - - rs384532 5:140190589 T 56147 NM_018900.2 Transcript intron_variant - - - - - - rs384532 5:140190589 T 56145 NM_018906.2 Transcript intron_variant - - - - - - rs384532 5:140190589 T 56144 NM_018907.2 Transcript intron_variant - - - - - - rs384532 5:140190589 T ENSESTG00000017804 ENSESTT00000044852 Transcript intron_variant - - - - - - rs384532 5:140190589 T 56146 NM_018905.2 Transcript intron_variant - - - - - - rs384532 5:140190589 T CCDS54916.1 CCDS54916.1 Transcript intron_variant - - - - - - rs384532 5:140190589 T 56144 NM_031500.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1420 rs384532 5:140190589 T ENSESTG00000018134 ENSESTT00000045630 Transcript intron_variant - - - - - - rs384532 5:140190589 T CCDS54912.1 CCDS54912.1 Transcript intron_variant - - - - - - rs384532 5:140190589 T CCDS54913.1 CCDS54913.1 Transcript intron_variant - - - - - - rs384532 5:140190589 T CCDS54915.1 CCDS54915.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C 56142 NM_031849.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS54914.1 CCDS54914.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C 56147 NM_018900.2 Transcript intron_variant - - - - - - rs628890 5:140231237 C 9752 NM_014005.3 Transcript 3_prime_UTR_variant 3881 - - - - - rs628890 5:140231237 C 56143 NM_018908.2 Transcript intron_variant - - - - - - rs628890 5:140231237 C 56140 NM_018911.2 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS54918.1 CCDS54918.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C ENSESTG00000017804 ENSESTT00000044852 Transcript intron_variant - - - - - - rs628890 5:140231237 C 9752 NM_031857.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS54916.1 CCDS54916.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS34255.1 CCDS34255.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4397 rs628890 5:140231237 C 56142 NM_018909.2 Transcript intron_variant - - - - - - rs628890 5:140231237 C 56139 NM_018901.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4397 rs628890 5:140231237 C 56139 NM_031860.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4397 rs628890 5:140231237 C CCDS54912.1 CCDS54912.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS54915.1 CCDS54915.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C 56147 NM_031411.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS54920.1 CCDS54920.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C 56145 NM_018906.2 Transcript intron_variant - - - - - - rs628890 5:140231237 C 56144 NM_018907.2 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS54917.1 CCDS54917.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C 56146 NM_018905.2 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS47282.1 CCDS47282.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS54921.1 CCDS54921.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4397 rs628890 5:140231237 C 56139 NM_031859.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4397 rs628890 5:140231237 C CCDS54919.1 CCDS54919.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS47281.1 CCDS47281.1 Transcript intron_variant - - - - - - rs628890 5:140231237 C 56141 NM_018910.2 Transcript intron_variant - - - - - - rs628890 5:140231237 C CCDS54913.1 CCDS54913.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T 56142 NM_031849.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS54914.1 CCDS54914.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T 56147 NM_018900.2 Transcript intron_variant - - - - - - rs251357 5:140233725 T 9752 NM_014005.3 Transcript 3_prime_UTR_variant 6369 - - - - - rs251357 5:140233725 T 56143 NM_018908.2 Transcript intron_variant - - - - - - rs251357 5:140233725 T 56140 NM_018911.2 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS54918.1 CCDS54918.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T ENSESTG00000017804 ENSESTT00000044852 Transcript intron_variant - - - - - - rs251357 5:140233725 T 9752 NM_031857.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T ENSESTG00000017804 ENSESTT00000044872 Transcript upstream_gene_variant - - - - - - DISTANCE=4242 rs251357 5:140233725 T CCDS54916.1 CCDS54916.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS34255.1 CCDS34255.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1909 rs251357 5:140233725 T 56142 NM_018909.2 Transcript intron_variant - - - - - - rs251357 5:140233725 T 56139 NM_018901.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1909 rs251357 5:140233725 T 56139 NM_031860.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1909 rs251357 5:140233725 T CCDS54912.1 CCDS54912.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS54915.1 CCDS54915.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T 56147 NM_031411.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS54920.1 CCDS54920.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T 56145 NM_018906.2 Transcript intron_variant - - - - - - rs251357 5:140233725 T 56144 NM_018907.2 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS54917.1 CCDS54917.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS47282.1 CCDS47282.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T 56146 NM_018905.2 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS54921.1 CCDS54921.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1909 rs251357 5:140233725 T 56139 NM_031859.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1909 rs251357 5:140233725 T CCDS54919.1 CCDS54919.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS47281.1 CCDS47281.1 Transcript intron_variant - - - - - - rs251357 5:140233725 T 56141 NM_018910.2 Transcript intron_variant - - - - - - rs251357 5:140233725 T CCDS54913.1 CCDS54913.1 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56114 NM_018912.2 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56109 NM_032086.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3607 rs6860609 5:140750044 C 56102 NM_032097.1 Transcript missense_variant 83 83 28 V/A gTt/gCt - rs6860609 5:140750044 C 56111 NM_018917.2 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56102 NM_018924.2 Transcript missense_variant 83 83 28 V/A gTt/gCt - PolyPhen=benign;SIFT=tolerated rs6860609 5:140750044 C CCDS47290.1 CCDS47290.1 Transcript intron_variant - - - - - - rs6860609 5:140750044 C CCDS58979.1 CCDS58979.1 Transcript intron_variant - - - - - - rs6860609 5:140750044 C CCDS54923.1 CCDS54923.1 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56113 NM_018915.2 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56104 NM_018922.2 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56109 NM_018919.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3607 rs6860609 5:140750044 C CCDS47289.1 CCDS47289.1 Transcript intron_variant - - - - - - rs6860609 5:140750044 C CCDS54924.1 CCDS54924.1 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56112 NM_018916.3 Transcript intron_variant - - - - - - rs6860609 5:140750044 C ENSESTG00000017912 ENSESTT00000045104 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56103 NM_018923.2 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56110 NM_018918.2 Transcript intron_variant - - - - - - rs6860609 5:140750044 C CCDS54926.1 CCDS54926.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3607 rs6860609 5:140750044 C CCDS54922.1 CCDS54922.1 Transcript intron_variant - - - - - - rs6860609 5:140750044 C 56110 NM_032054.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3705 rs6860609 5:140750044 C CCDS54925.1 CCDS54925.1 Transcript intron_variant - - - - - - rs6860609 5:140750044 C CCDS58980.1 CCDS58980.1 Transcript missense_variant 83 83 28 V/A gTt/gCt - PolyPhen=benign;SIFT=tolerated rs57666129 5:140902832 T ENSESTG00000017983 ENSESTT00000045462 Transcript intron_variant - - - - - - rs57666129 5:140902832 T ENSESTG00000017983 ENSESTT00000045508 Transcript intron_variant - - - - - - rs57666129 5:140902832 T ENSESTG00000017983 ENSESTT00000045479 Transcript intron_variant - - - - - - rs57666129 5:140902832 T ENSESTG00000017965 ENSESTT00000045243 Transcript downstream_gene_variant - - - - - - DISTANCE=3999 rs57666129 5:140902832 T CCDS43374.1 CCDS43374.1 Transcript intron_variant - - - - - - rs57666129 5:140902832 T ENSESTG00000017983 ENSESTT00000045525 Transcript intron_variant - - - - - - rs57666129 5:140902832 T 1729 NM_005219.4 Transcript intron_variant - - - - - - rs57666129 5:140902832 T CCDS43373.1 CCDS43373.1 Transcript intron_variant - - - - - - rs57666129 5:140902832 T ENSESTG00000017983 ENSESTT00000045535 Transcript intron_variant - - - - - - rs57666129 5:140902832 T ENSESTG00000017983 ENSESTT00000045432 Transcript intron_variant - - - - - - rs57666129 5:140902832 T 1729 NM_001079812.2 Transcript intron_variant - - - - - - rs57666129 5:140902832 T ENSESTG00000017983 ENSESTT00000045446 Transcript intron_variant - - - - - - rs57666129 5:140902832 T ENSESTG00000017983 ENSESTT00000045553 Transcript intron_variant - - - - - - rs250789 5:140923291 A ENSESTG00000017983 ENSESTT00000045462 Transcript intron_variant - - - - - - rs250789 5:140923291 A ENSESTG00000017983 ENSESTT00000045446 Transcript intron_variant - - - - - - rs250789 5:140923291 A CCDS43374.1 CCDS43374.1 Transcript intron_variant - - - - - - rs250789 5:140923291 A 1729 NM_005219.4 Transcript intron_variant - - - - - - rs250789 5:140923291 A CCDS43373.1 CCDS43373.1 Transcript intron_variant - - - - - - rs250789 5:140923291 A ENSESTG00000017983 ENSESTT00000045432 Transcript intron_variant - - - - - - rs250789 5:140923291 A 1729 NM_001079812.2 Transcript intron_variant - - - - - - rs250792 5:140996319 C - ENSR00001292077 RegulatoryFeature regulatory_region_variant - - - - - - rs250792 5:140996319 C CCDS43374.1 CCDS43374.1 Transcript intron_variant - - - - - - rs250792 5:140996319 C 1729 NM_005219.4 Transcript intron_variant - - - - - - rs250792 5:140996319 C ENSESTG00000006218 ENSESTT00000015677 Transcript intron_variant - - - - - - rs250792 5:140996319 C CCDS43373.1 CCDS43373.1 Transcript intron_variant - - - - - - rs250792 5:140996319 C 1729 NM_001079812.2 Transcript intron_variant - - - - - - rs250792 5:140996319 C CCDS4264.1 CCDS4264.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4716 rs250792 5:140996319 C ENSESTG00000006200 ENSESTT00000015658 Transcript downstream_gene_variant - - - - - - DISTANCE=4703 rs250792 5:140996319 C ENSESTG00000006200 ENSESTT00000015638 Transcript downstream_gene_variant - - - - - - DISTANCE=4703 rs250792 5:140996319 C ENSESTG00000005980 ENSESTT00000015155 Transcript upstream_gene_variant - - - - - - DISTANCE=1661 rs250792 5:140996319 C 8841 NM_003883.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4124 rs250793 5:141011187 C CCDS4264.1 CCDS4264.1 Transcript intron_variant - - - - - - rs250793 5:141011187 C ENSESTG00000006200 ENSESTT00000015658 Transcript intron_variant - - - - - - rs250793 5:141011187 C ENSESTG00000006200 ENSESTT00000015638 Transcript intron_variant - - - - - - rs250793 5:141011187 C 8841 NM_003883.3 Transcript intron_variant - - - - - - rs32954 5:141016276 C - ENSR00001292082 RegulatoryFeature regulatory_region_variant - - - - - - rs32954 5:141016276 C ENSESTG00000005984 ENSESTT00000015174 Transcript upstream_gene_variant - - - - - - DISTANCE=3526 rs32954 5:141016276 C CCDS4265.1 CCDS4265.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1517 rs32954 5:141016276 C 285613 NM_173828.4 Transcript upstream_gene_variant - - - - - - DISTANCE=241 rs32954 5:141016276 C ENSESTG00000006200 ENSESTT00000015638 Transcript intron_variant - - - - - - rs32954 5:141016276 C ENSESTG00000006200 ENSESTT00000015658 Transcript intron_variant - - - - - - rs32954 5:141016276 C CCDS4264.1 CCDS4264.1 Transcript intron_variant - - - - - - rs32954 5:141016276 C 285613 NM_001130029.1 Transcript upstream_gene_variant - - - - - - DISTANCE=241 rs32954 5:141016276 C 8841 NM_003883.3 Transcript intron_variant - - - - - - rs32954 5:141016276 C 89848 NM_033449.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2593 rs32954 5:141016276 C CCDS47295.1 CCDS47295.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4789 rs351262 5:141284410 C - - - intergenic_variant - - - - - - rs441530 5:141321170 C - ENSR00001292177 RegulatoryFeature regulatory_region_variant - - - - - - rs441530 5:141321170 C ENSESTG00000006180 ENSESTT00000015550 Transcript splice_region_variant,intron_variant - - - - - - rs441530 5:141321170 C 51294 NM_016580.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3360 rs441530 5:141321170 C 9812 NM_001142603.1 Transcript 3_prime_UTR_variant 3723 - - - - - rs441530 5:141321170 C ENSESTG00000006040 ENSESTT00000015307 Transcript downstream_gene_variant - - - - - - DISTANCE=2240 rs441530 5:141321170 C CCDS4268.1 CCDS4268.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2846 rs441530 5:141321170 C CCDS4269.1 CCDS4269.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3776 rs441530 5:141321170 C ENSESTG00000006040 ENSESTT00000015303 Transcript downstream_gene_variant - - - - - - DISTANCE=1454 rs441530 5:141321170 C 9812 NM_014773.3 Transcript 3_prime_UTR_variant 4516 - - - - - rs607109 5:141966635 G - - - intergenic_variant - - - - - - rs250130 5:142016527 T 2246 NM_001144935.1 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_001257211.1 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_000800.4 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_033136.3 Transcript intron_variant - - - - - - rs250130 5:142016527 T ENSESTG00000031633 ENSESTT00000079803 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_001257209.1 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_001257205.1 Transcript intron_variant - - - - - - rs250130 5:142016527 T ENSESTG00000031633 ENSESTT00000079834 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_001257208.1 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_001257207.1 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_001257210.1 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_001257206.1 Transcript intron_variant - - - - - - rs250130 5:142016527 T 2246 NM_001144934.1 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_001144935.1 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_001257211.1 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_000800.4 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_033136.3 Transcript intron_variant - - - - - - rs4912873 5:142041170 A ENSESTG00000031633 ENSESTT00000079803 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_001257209.1 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_001257205.1 Transcript intron_variant - - - - - - rs4912873 5:142041170 A ENSESTG00000031633 ENSESTT00000079834 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_001257208.1 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_001257207.1 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_001257206.1 Transcript intron_variant - - - - - - rs4912873 5:142041170 A 2246 NM_001144934.1 Transcript intron_variant - - - - - - rs369843 5:142291365 G 23092 NM_015071.4 Transcript intron_variant - - - - - - rs369843 5:142291365 G CCDS47297.1 CCDS47297.1 Transcript intron_variant - - - - - - rs369843 5:142291365 G ENSESTG00000031477 ENSESTT00000079578 Transcript intron_variant - - - - - - rs369843 5:142291365 G ENSESTG00000031477 ENSESTT00000079462 Transcript downstream_gene_variant - - - - - - DISTANCE=3991 rs369843 5:142291365 G ENSESTG00000031477 ENSESTT00000079584 Transcript intron_variant - - - - - - rs369843 5:142291365 G CCDS4277.1 CCDS4277.1 Transcript intron_variant - - - - - - rs369843 5:142291365 G ENSESTG00000031477 ENSESTT00000079582 Transcript intron_variant - - - - - - rs369843 5:142291365 G ENSESTG00000031477 ENSESTT00000079571 Transcript intron_variant - - - - - - rs369843 5:142291365 G 23092 NM_001135608.1 Transcript intron_variant - - - - - - rs369843 5:142291365 G ENSESTG00000031477 ENSESTT00000079456 Transcript downstream_gene_variant - - - - - - DISTANCE=3991 rs369843 5:142291365 G ENSESTG00000031477 ENSESTT00000079555 Transcript intron_variant - - - - - - rs369843 5:142291365 G ENSESTG00000031477 ENSESTT00000079452 Transcript downstream_gene_variant - - - - - - DISTANCE=3991 rs369843 5:142291365 G ENSESTG00000031477 ENSESTT00000079565 Transcript intron_variant - - - - - - rs153163 5:142332739 C 23092 NM_015071.4 Transcript intron_variant - - - - - - rs153163 5:142332739 C CCDS47297.1 CCDS47297.1 Transcript intron_variant - - - - - - rs153163 5:142332739 C ENSESTG00000031477 ENSESTT00000079578 Transcript intron_variant - - - - - - rs153163 5:142332739 C ENSESTG00000031477 ENSESTT00000079584 Transcript intron_variant - - - - - - rs153163 5:142332739 C CCDS4277.1 CCDS4277.1 Transcript intron_variant - - - - - - rs153163 5:142332739 C ENSESTG00000031477 ENSESTT00000079582 Transcript intron_variant - - - - - - rs153163 5:142332739 C 23092 NM_001135608.1 Transcript intron_variant - - - - - - rs153163 5:142332739 C ENSESTG00000031477 ENSESTT00000079555 Transcript intron_variant - - - - - - rs153163 5:142332739 C ENSESTG00000031477 ENSESTT00000079565 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001018074.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001204259.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C ENSESTG00000031612 ENSESTT00000079770 Transcript intron_variant - - - - - - rs6882247 5:142765821 C ENSESTG00000031612 ENSESTT00000079737 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001204261.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001204265.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001018077.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001018075.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001204264.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001204260.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001204258.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001204263.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C CCDS47298.1 CCDS47298.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C CCDS4278.1 CCDS4278.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001024094.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_000176.2 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001018076.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001020825.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C 2908 NM_001204262.1 Transcript intron_variant - - - - - - rs6882247 5:142765821 C CCDS34258.1 CCDS34258.1 Transcript intron_variant - - - - - - rs586235 5:142934951 G - ENSR00001414750 RegulatoryFeature regulatory_region_variant - - - - - - rs586235 5:142934951 G ENSESTG00000034140 ENSESTT00000086279 Transcript upstream_gene_variant - - - - - - DISTANCE=3833 rs325274 5:143177973 T - - - intergenic_variant - - - - - - rs455644 5:143313859 G - - - intergenic_variant - - - - - - rs316060 5:143424303 T - - - intergenic_variant - - - - - - rs6897532 5:143840363 G 57528 NM_020768.3 Transcript intron_variant - - - - - - rs6897532 5:143840363 G CCDS34260.1 CCDS34260.1 Transcript intron_variant - - - - - - rs2400166 5:144401219 T - - - intergenic_variant - - - - - - rs653438 5:144415694 T - - - intergenic_variant - - - - - - rs340050 5:145219553 C 153768 NM_138492.4 Transcript upstream_gene_variant - - - - - - DISTANCE=4654 rs340050 5:145219553 C ENSESTG00000035441 ENSESTT00000089498 Transcript upstream_gene_variant - - - - - - DISTANCE=4686 rs340050 5:145219553 C 153768 NM_205846.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4686 rs340050 5:145219553 C ENSESTG00000035441 ENSESTT00000089495 Transcript upstream_gene_variant - - - - - - DISTANCE=4672 rs340050 5:145219553 C CCDS34262.1 CCDS34262.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4739 rs340050 5:145219553 C ENSESTG00000035441 ENSESTT00000089502 Transcript upstream_gene_variant - - - - - - DISTANCE=4759 rs340050 5:145219553 C ENSESTG00000035441 ENSESTT00000089493 Transcript upstream_gene_variant - - - - - - DISTANCE=4621 rs340050 5:145219553 C CCDS34261.1 CCDS34261.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4739 rs340050 5:145219553 C 153768 NM_182960.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4686 rs2963928 5:145625716 G CCDS43378.1 CCDS43378.1 Transcript intron_variant - - - - - - rs2963928 5:145625716 G 54439 NM_018989.1 Transcript intron_variant - - - - - - rs2963928 5:145625716 G ENSESTG00000035368 ENSESTT00000089312 Transcript intron_variant - - - - - - rs2963928 5:145625716 G ENSESTG00000035368 ENSESTT00000089314 Transcript intron_variant - - - - - - rs161022 5:146216878 G 5521 NM_181677.2 Transcript intron_variant - - - - - - rs161022 5:146216878 G ENSESTG00000001045 ENSESTT00000002575 Transcript intron_variant - - - - - - rs161022 5:146216878 G CCDS4283.1 CCDS4283.1 Transcript intron_variant - - - - - - rs161022 5:146216878 G ENSESTG00000001045 ENSESTT00000002557 Transcript intron_variant - - - - - - rs161022 5:146216878 G CCDS4284.1 CCDS4284.1 Transcript intron_variant - - - - - - rs161022 5:146216878 G 5521 NM_181674.2 Transcript intron_variant - - - - - - rs161022 5:146216878 G ENSESTG00000001045 ENSESTT00000002571 Transcript intron_variant - - - - - - rs161022 5:146216878 G 5521 NM_001127381.1 Transcript intron_variant - - - - - - rs161022 5:146216878 G 5521 NM_181678.2 Transcript intron_variant - - - - - - rs161022 5:146216878 G ENSESTG00000001045 ENSESTT00000002555 Transcript intron_variant - - - - - - rs161022 5:146216878 G 5521 NM_181675.2 Transcript intron_variant - - - - - - rs161022 5:146216878 G 5521 NM_181676.2 Transcript intron_variant - - - - - - rs161022 5:146216878 G ENSESTG00000001080 ENSESTT00000002578 Transcript intron_variant - - - - - - rs161022 5:146216878 G CCDS43380.1 CCDS43380.1 Transcript intron_variant - - - - - - rs161022 5:146216878 G 5521 NM_004576.2 Transcript intron_variant - - - - - - rs161022 5:146216878 G ENSESTG00000001045 ENSESTT00000002551 Transcript intron_variant - - - - - - rs161022 5:146216878 G ENSESTG00000001045 ENSESTT00000002560 Transcript intron_variant - - - - - - rs31030 5:146609540 T ENSESTG00000001038 ENSESTT00000002478 Transcript intron_variant - - - - - - rs6580477 5:146951213 T 153469 NR_038902.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1119786 5:147459352 A ENSESTG00000011517 ENSESTT00000028907 Transcript intron_variant - - - - - - rs1119786 5:147459352 A CCDS47301.1 CCDS47301.1 Transcript intron_variant - - - - - - rs1119786 5:147459352 A 11005 NM_001127699.1 Transcript intron_variant - - - - - - rs1119786 5:147459352 A 11005 NM_006846.3 Transcript intron_variant - - - - - - rs1119786 5:147459352 A CCDS43382.1 CCDS43382.1 Transcript intron_variant - - - - - - rs1119786 5:147459352 A ENSESTG00000011517 ENSESTT00000028911 Transcript intron_variant - - - - - - rs1119786 5:147459352 A ENSESTG00000011664 ENSESTT00000029209 Transcript intron_variant - - - - - - rs1119786 5:147459352 A CCDS47300.1 CCDS47300.1 Transcript intron_variant - - - - - - rs1119786 5:147459352 A ENSESTG00000011517 ENSESTT00000028904 Transcript intron_variant - - - - - - rs1119786 5:147459352 A 11005 NM_001127698.1 Transcript intron_variant - - - - - - rs1370974 5:148646434 G ENSESTG00000031962 ENSESTT00000080749 Transcript upstream_gene_variant - - - - - - DISTANCE=4969 rs1370974 5:148646434 G 134265 NM_001146337.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4967 rs1370974 5:148646434 G 134265 NM_152406.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4967 rs246393 5:149497815 G CCDS4303.1 CCDS4303.1 Transcript intron_variant - - - - - - rs246393 5:149497815 G 5159 NM_002609.3 Transcript intron_variant - - - - - - rs246393 5:149497815 G 1436 NM_005211.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4880 rs6579776 5:149549814 G 1044 NM_001804.2 Transcript intron_variant - - - - - - rs6579776 5:149549814 G CCDS4304.1 CCDS4304.1 Transcript intron_variant - - - - - - rs6579783 5:149616569 C ENSESTG00000026530 ENSESTT00000066927 Transcript intron_variant - - - - - - rs6579783 5:149616569 C CCDS43387.1 CCDS43387.1 Transcript intron_variant - - - - - - rs6579783 5:149616569 C CCDS43386.1 CCDS43386.1 Transcript intron_variant - - - - - - rs6579783 5:149616569 C 815 NM_015981.3 Transcript intron_variant - - - - - - rs6579783 5:149616569 C ENSESTG00000026530 ENSESTT00000066987 Transcript intron_variant - - - - - - rs6579783 5:149616569 C ENSESTG00000026530 ENSESTT00000066905 Transcript intron_variant - - - - - - rs6579783 5:149616569 C 815 NM_171825.2 Transcript intron_variant - - - - - - rs2913891 5:151257399 A ENSESTG00000012418 ENSESTT00000031112 Transcript intron_variant - - - - - - rs2913891 5:151257399 A 2741 NM_000171.3 Transcript intron_variant - - - - - - rs2913891 5:151257399 A ENSESTG00000012399 ENSESTT00000031089 Transcript intron_variant - - - - - - rs2913891 5:151257399 A ENSESTG00000012418 ENSESTT00000031117 Transcript intron_variant - - - - - - rs2913891 5:151257399 A CCDS4320.1 CCDS4320.1 Transcript intron_variant - - - - - - rs2913891 5:151257399 A CCDS54942.1 CCDS54942.1 Transcript intron_variant - - - - - - rs2913891 5:151257399 A 2741 NM_001146040.1 Transcript intron_variant - - - - - - rs2964600 5:151261273 A ENSESTG00000012418 ENSESTT00000031112 Transcript intron_variant - - - - - - rs2964600 5:151261273 A 2741 NM_000171.3 Transcript intron_variant - - - - - - rs2964600 5:151261273 A ENSESTG00000012399 ENSESTT00000031089 Transcript intron_variant - - - - - - rs2964600 5:151261273 A ENSESTG00000012418 ENSESTT00000031117 Transcript intron_variant - - - - - - rs2964600 5:151261273 A CCDS4320.1 CCDS4320.1 Transcript intron_variant - - - - - - rs2964600 5:151261273 A CCDS54942.1 CCDS54942.1 Transcript intron_variant - - - - - - rs2964600 5:151261273 A 2741 NM_001146040.1 Transcript intron_variant - - - - - - rs7445361 5:152182272 A ENSESTG00000003079 ENSESTT00000007658 Transcript intron_variant - - - - - - rs10477035 5:152193763 T ENSESTG00000003079 ENSESTT00000007658 Transcript intron_variant - - - - - - rs1371061 5:152406277 T - - - intergenic_variant - - - - - - rs2579042 5:152522723 C - - - intergenic_variant - - - - - - rs2910025 5:152529123 T - - - intergenic_variant - - - - - - rs4360089 5:153384326 C ENSESTG00000000114 ENSESTT00000000319 Transcript intron_variant - - - - - - rs4360089 5:153384326 C ENSESTG00000000114 ENSESTT00000000321 Transcript intron_variant - - - - - - rs4360089 5:153384326 C 10827 NM_018691.2 Transcript intron_variant - - - - - - rs4360089 5:153384326 C CCDS4323.1 CCDS4323.1 Transcript intron_variant - - - - - - rs4958714 5:153591225 A - ENSR00001294449 RegulatoryFeature regulatory_region_variant - - - - - - rs4958714 5:153591225 A ENSESTG00000000087 ENSESTT00000000266 Transcript intron_variant - - - - - - rs4958714 5:153591225 A ENSESTG00000000087 ENSESTT00000000275 Transcript intron_variant - - - - - - rs4958714 5:153591225 A ENSESTG00000000087 ENSESTT00000000276 Transcript intron_variant - - - - - - rs4958714 5:153591225 A CCDS4325.1 CCDS4325.1 Transcript intron_variant - - - - - - rs4958714 5:153591225 A ENSESTG00000000087 ENSESTT00000000277 Transcript intron_variant - - - - - - rs4958714 5:153591225 A ENSESTG00000000087 ENSESTT00000000280 Transcript intron_variant - - - - - - rs4958714 5:153591225 A ENSESTG00000000087 ENSESTT00000000268 Transcript intron_variant - - - - - - rs4958714 5:153591225 A 55568 NM_198321.3 Transcript intron_variant - - - - - - rs4958714 5:153591225 A ENSESTG00000000087 ENSESTT00000000279 Transcript intron_variant - - - - - - rs1150160 5:153623624 C - ENSR00001415537 RegulatoryFeature regulatory_region_variant - - - - - - rs1150160 5:153623624 C ENSESTG00000000087 ENSESTT00000000266 Transcript intron_variant - - - - - - rs1150160 5:153623624 C ENSESTG00000000087 ENSESTT00000000275 Transcript intron_variant - - - - - - rs1150160 5:153623624 C ENSESTG00000000087 ENSESTT00000000276 Transcript intron_variant - - - - - - rs1150160 5:153623624 C CCDS4325.1 CCDS4325.1 Transcript intron_variant - - - - - - rs1150160 5:153623624 C ENSESTG00000000087 ENSESTT00000000277 Transcript intron_variant - - - - - - rs1150160 5:153623624 C ENSESTG00000000087 ENSESTT00000000280 Transcript intron_variant - - - - - - rs1150160 5:153623624 C ENSESTG00000000087 ENSESTT00000000268 Transcript intron_variant - - - - - - rs1150160 5:153623624 C 55568 NM_198321.3 Transcript intron_variant - - - - - - rs1150160 5:153623624 C ENSESTG00000000087 ENSESTT00000000279 Transcript intron_variant - - - - - - rs9324790 5:154078373 T - ENSR00001415581 RegulatoryFeature regulatory_region_variant - - - - - - rs9324790 5:154078373 T - - - intergenic_variant - - - - - - rs1233074 5:154106192 A 23367 NM_015315.3 Transcript intron_variant - - - - - - rs1233074 5:154106192 A CCDS4328.1 CCDS4328.1 Transcript intron_variant - - - - - - rs164526 5:154528043 G - - - intergenic_variant - - - - - - rs4371815 5:155087782 C - - - intergenic_variant - - - - - - rs3097861 5:155552221 T - - - intergenic_variant - - - - - - rs249893 5:155665369 C - - - intergenic_variant - - - - - - rs253597 5:155969749 C 6444 NM_000337.5 Transcript intron_variant - - - - - - rs253597 5:155969749 C CCDS47326.1 CCDS47326.1 Transcript intron_variant - - - - - - rs253597 5:155969749 C ENSESTG00000021884 ENSESTT00000055168 Transcript intron_variant - - - - - - rs253597 5:155969749 C CCDS47325.1 CCDS47325.1 Transcript intron_variant - - - - - - rs253597 5:155969749 C 6444 NM_001128209.1 Transcript intron_variant - - - - - - rs253597 5:155969749 C CCDS47327.1 CCDS47327.1 Transcript intron_variant - - - - - - rs253597 5:155969749 C 6444 NM_172244.2 Transcript intron_variant - - - - - - rs1036183 5:156019805 A 6444 NM_000337.5 Transcript intron_variant - - - - - - rs1036183 5:156019805 A CCDS47326.1 CCDS47326.1 Transcript intron_variant - - - - - - rs1036183 5:156019805 A ENSESTG00000021884 ENSESTT00000055168 Transcript intron_variant - - - - - - rs1036183 5:156019805 A CCDS47325.1 CCDS47325.1 Transcript intron_variant - - - - - - rs1036183 5:156019805 A 6444 NM_001128209.1 Transcript intron_variant - - - - - - rs1036183 5:156019805 A CCDS47327.1 CCDS47327.1 Transcript intron_variant - - - - - - rs1036183 5:156019805 A 6444 NM_172244.2 Transcript intron_variant - - - - - - rs1220612 5:156335451 C - - - intergenic_variant - - - - - - rs1186790 5:157287355 G 9685 NM_001195555.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1172 rs1186790 5:157287355 G CCDS47330.1 CCDS47330.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1377 rs1186790 5:157287355 G CCDS56389.1 CCDS56389.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1377 rs1186790 5:157287355 G ENSESTG00000019880 ENSESTT00000049957 Transcript upstream_gene_variant - - - - - - DISTANCE=1204 rs1186790 5:157287355 G 9685 NM_001195556.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1172 rs1186790 5:157287355 G 9685 NM_014666.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1172 rs2964493 5:157924493 T ENSESTG00000019852 ENSESTT00000049760 Transcript intron_variant - - - - - - rs2964493 5:157924493 T ENSESTG00000019852 ENSESTT00000049799 Transcript intron_variant - - - - - - rs4235720 5:157928140 G ENSESTG00000019852 ENSESTT00000049760 Transcript intron_variant - - - - - - rs4235720 5:157928140 G ENSESTG00000019852 ENSESTT00000049799 Transcript intron_variant - - - - - - rs7446069 5:158238928 T 1879 NM_024007.3 Transcript intron_variant - - - - - - rs7446069 5:158238928 T CCDS4343.1 CCDS4343.1 Transcript intron_variant - - - - - - rs6556368 5:158282543 C 1879 NM_024007.3 Transcript intron_variant - - - - - - rs6556368 5:158282543 C CCDS4343.1 CCDS4343.1 Transcript intron_variant - - - - - - rs7442733 5:158311287 T 1879 NM_024007.3 Transcript intron_variant - - - - - - rs7442733 5:158311287 T CCDS4343.1 CCDS4343.1 Transcript intron_variant - - - - - - rs13183005 5:158389079 A 1879 NM_024007.3 Transcript intron_variant - - - - - - rs13183005 5:158389079 A CCDS4343.1 CCDS4343.1 Transcript intron_variant - - - - - - rs6556403 5:158611939 A - ENSR00001415879 RegulatoryFeature regulatory_region_variant - - - - - - rs6556403 5:158611939 A CCDS56391.1 CCDS56391.1 Transcript intron_variant - - - - - - rs6556403 5:158611939 A 153830 NM_001199383.1 Transcript intron_variant - - - - - - rs6556403 5:158611939 A ENSESTG00000005011 ENSESTT00000012777 Transcript intron_variant - - - - - - rs6556403 5:158611939 A 153830 NM_144726.2 Transcript intron_variant - - - - - - rs6556403 5:158611939 A ENSESTG00000005011 ENSESTT00000012779 Transcript intron_variant - - - - - - rs6556403 5:158611939 A 153830 NM_001199380.1 Transcript intron_variant - - - - - - rs6556403 5:158611939 A CCDS56390.1 CCDS56390.1 Transcript intron_variant - - - - - - rs6556403 5:158611939 A 153830 NM_001199381.1 Transcript intron_variant - - - - - - rs6556403 5:158611939 A ENSESTG00000005011 ENSESTT00000012762 Transcript intron_variant - - - - - - rs6556403 5:158611939 A 153830 NM_001199382.1 Transcript intron_variant - - - - - - rs6556403 5:158611939 A ENSESTG00000005011 ENSESTT00000012758 Transcript intron_variant - - - - - - rs6556403 5:158611939 A CCDS56392.1 CCDS56392.1 Transcript intron_variant - - - - - - rs6556403 5:158611939 A CCDS56393.1 CCDS56393.1 Transcript intron_variant - - - - - - rs6556403 5:158611939 A ENSESTG00000005011 ENSESTT00000012780 Transcript intron_variant - - - - - - rs6556403 5:158611939 A CCDS4344.1 CCDS4344.1 Transcript intron_variant - - - - - - rs6556427 5:158921439 G ENSESTG00000005001 ENSESTT00000012712 Transcript intron_variant - - - - - - rs2901488 5:159422768 G - - - intergenic_variant - - - - - - rs9790876 5:159515763 T CCDS47332.1 CCDS47332.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3626 rs9790876 5:159515763 T ENSESTG00000028671 ENSESTT00000072128 Transcript downstream_gene_variant - - - - - - DISTANCE=4996 rs9790876 5:159515763 T CCDS58990.1 CCDS58990.1 Transcript intron_variant - - - - - - rs9790876 5:159515763 T CCDS47331.1 CCDS47331.1 Transcript intron_variant - - - - - - rs9790876 5:159515763 T ENSESTG00000028686 ENSESTT00000072157 Transcript intron_variant - - - - - - rs9790876 5:159515763 T 114825 NM_052927.2 Transcript intron_variant - - - - - - rs9790876 5:159515763 T 114825 NM_001130864.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2583 rs9790876 5:159515763 T 114825 NM_001267035.1 Transcript intron_variant - - - - - - rs9790876 5:159515763 T ENSESTG00000028686 ENSESTT00000072170 Transcript intron_variant - - - - - - rs9790876 5:159515763 T ENSESTG00000028686 ENSESTT00000072197 Transcript intron_variant - - - - - - rs4921295 5:159934135 C - ENSR00001416011 RegulatoryFeature regulatory_region_variant - - - - - - rs4921295 5:159934135 C - - - intergenic_variant - - - - - - rs1421953 5:160124050 A ENSESTG00000030115 ENSESTT00000075792 Transcript intron_variant - - - - - - rs1421953 5:160124050 A 23120 NM_025153.2 Transcript intron_variant - - - - - - rs1421953 5:160124050 A ENSESTG00000030115 ENSESTT00000075807 Transcript intron_variant - - - - - - rs1421953 5:160124050 A ENSESTG00000030115 ENSESTT00000075781 Transcript intron_variant - - - - - - rs1421953 5:160124050 A ENSESTG00000030115 ENSESTT00000075817 Transcript intron_variant - - - - - - rs4579294 5:160264398 A - ENSR00001416024 RegulatoryFeature regulatory_region_variant - - - - - - rs4579294 5:160264398 A ENSESTG00000030115 ENSESTT00000075792 Transcript intron_variant - - - - - - rs4579294 5:160264398 A 23120 NM_025153.2 Transcript intron_variant - - - - - - rs4579294 5:160264398 A ENSESTG00000030115 ENSESTT00000075807 Transcript intron_variant - - - - - - rs4579294 5:160264398 A ENSESTG00000030115 ENSESTT00000075781 Transcript intron_variant - - - - - - rs4579294 5:160264398 A ENSESTG00000030115 ENSESTT00000075838 Transcript intron_variant - - - - - - rs4579294 5:160264398 A ENSESTG00000030115 ENSESTT00000075817 Transcript intron_variant - - - - - - rs6897724 5:160320030 A - - - intergenic_variant - - - - - - rs4244419 5:160480672 G - - - intergenic_variant - - - - - - rs1363699 5:160799651 A ENSESTG00000030071 ENSESTT00000075750 Transcript intron_variant - - - - - - rs1363699 5:160799651 A ENSESTG00000030071 ENSESTT00000075743 Transcript intron_variant - - - - - - rs1363699 5:160799651 A CCDS4354.1 CCDS4354.1 Transcript intron_variant - - - - - - rs1363699 5:160799651 A CCDS4355.1 CCDS4355.1 Transcript intron_variant - - - - - - rs1363699 5:160799651 A 2561 NM_000813.2 Transcript intron_variant - - - - - - rs1363699 5:160799651 A 2561 NM_021911.2 Transcript intron_variant - - - - - - rs1363699 5:160799651 A ENSESTG00000030071 ENSESTT00000075703 Transcript intron_variant - - - - - - rs7730579 5:161044314 A - - - intergenic_variant - - - - - - rs1545322 5:161096024 A - - - intergenic_variant - - - - - - rs1457702 5:161346174 G - - - intergenic_variant - - - - - - rs6889382 5:161350983 G - - - intergenic_variant - - - - - - rs1457708 5:161403653 A - - - intergenic_variant - - - - - - rs1385135 5:161978384 T - - - intergenic_variant - - - - - - rs312309 5:162070945 G - - - intergenic_variant - - - - - - rs699115 5:162176020 A - - - intergenic_variant - - - - - - rs11135230 5:162292875 C - - - intergenic_variant - - - - - - rs828766 5:162358458 A - - - intergenic_variant - - - - - - rs2964353 5:162621772 C - - - intergenic_variant - - - - - - rs380101 5:162890953 A CCDS4363.1 CCDS4363.1 Transcript synonymous_variant 138 138 46 Q caG/caA - rs380101 5:162890953 A 3161 NM_001142556.1 Transcript synonymous_variant 320 138 46 Q caG/caA - rs380101 5:162890953 A ENSESTG00000017140 ENSESTT00000043258 Transcript synonymous_variant 258 138 46 Q caG/caA - rs380101 5:162890953 A ENSESTG00000017140 ENSESTT00000043249 Transcript synonymous_variant 258 138 46 Q caG/caA - rs380101 5:162890953 A ENSESTG00000017140 ENSESTT00000043198 Transcript 5_prime_UTR_variant 274 - - - - - rs380101 5:162890953 A CCDS4361.1 CCDS4361.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3897 rs380101 5:162890953 A ENSESTG00000017140 ENSESTT00000043212 Transcript synonymous_variant 390 138 46 Q caG/caA - rs380101 5:162890953 A 134492 NM_145266.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3810 rs380101 5:162890953 A 3161 NM_012484.2 Transcript synonymous_variant 320 138 46 Q caG/caA - rs380101 5:162890953 A 3161 NM_001142557.1 Transcript intron_variant - - - - - - rs380101 5:162890953 A ENSESTG00000017140 ENSESTT00000043192 Transcript 5_prime_UTR_variant 274 - - - - - rs380101 5:162890953 A CCDS47335.1 CCDS47335.1 Transcript intron_variant - - - - - - rs380101 5:162890953 A CCDS47334.1 CCDS47334.1 Transcript synonymous_variant 138 138 46 Q caG/caA - rs380101 5:162890953 A 3161 NM_012485.2 Transcript synonymous_variant 320 138 46 Q caG/caA - rs380101 5:162890953 A CCDS4362.1 CCDS4362.1 Transcript synonymous_variant 138 138 46 Q caG/caA - rs6860394 5:162954711 T - - - intergenic_variant - - - - - - rs159205 5:163061560 A - - - intergenic_variant - - - - - - rs577115 5:163139660 G - - - intergenic_variant - - - - - - rs2849636 5:163222551 C - - - intergenic_variant - - - - - - rs1225879 5:163567726 C ENSESTG00000000455 ENSESTT00000001118 Transcript intron_variant - - - - - - rs2932149 5:163929974 A ENSESTG00000000441 ENSESTT00000001090 Transcript intron_variant - - - - - - rs2932149 5:163929974 A ENSESTG00000000441 ENSESTT00000001095 Transcript intron_variant - - - - - - rs2932149 5:163929974 A ENSESTG00000000441 ENSESTT00000001107 Transcript intron_variant - - - - - - rs2932149 5:163929974 A ENSESTG00000000441 ENSESTT00000001102 Transcript intron_variant - - - - - - rs2913716 5:163936111 G ENSESTG00000000441 ENSESTT00000001090 Transcript intron_variant - - - - - - rs2913716 5:163936111 G ENSESTG00000000441 ENSESTT00000001095 Transcript intron_variant - - - - - - rs2913716 5:163936111 G ENSESTG00000000441 ENSESTT00000001107 Transcript intron_variant - - - - - - rs2913716 5:163936111 G ENSESTG00000000441 ENSESTT00000001102 Transcript intron_variant - - - - - - rs2932128 5:163937023 G ENSESTG00000000441 ENSESTT00000001090 Transcript intron_variant - - - - - - rs2932128 5:163937023 G ENSESTG00000000441 ENSESTT00000001095 Transcript intron_variant - - - - - - rs2932128 5:163937023 G ENSESTG00000000441 ENSESTT00000001107 Transcript intron_variant - - - - - - rs2932128 5:163937023 G ENSESTG00000000441 ENSESTT00000001102 Transcript intron_variant - - - - - - rs2932150 5:163959228 A - ENSR00001416115 RegulatoryFeature regulatory_region_variant - - - - - - rs2932150 5:163959228 A ENSESTG00000000441 ENSESTT00000001090 Transcript intron_variant - - - - - - rs2932150 5:163959228 A ENSESTG00000000441 ENSESTT00000001095 Transcript intron_variant - - - - - - rs2932150 5:163959228 A ENSESTG00000000441 ENSESTT00000001107 Transcript intron_variant - - - - - - rs2932150 5:163959228 A ENSESTG00000000441 ENSESTT00000001102 Transcript intron_variant - - - - - - rs2964308 5:163979095 T ENSESTG00000000441 ENSESTT00000001095 Transcript intron_variant - - - - - - rs9918186 5:164351804 T - - - intergenic_variant - - - - - - rs6894460 5:164450403 G ENSESTG00000000384 ENSESTT00000000983 Transcript intron_variant - - - - - - rs6885823 5:164453755 T ENSESTG00000000384 ENSESTT00000000983 Transcript intron_variant - - - - - - rs7736583 5:164560582 C ENSESTG00000000384 ENSESTT00000000983 Transcript downstream_gene_variant - - - - - - DISTANCE=3348 rs830228 5:165400396 G - - - intergenic_variant - - - - - - rs31735 5:165456146 G ENSESTG00000014087 ENSESTT00000035223 Transcript synonymous_variant 154 12 4 S tcT/tcC - rs7715944 5:165651121 G - - - intergenic_variant - - - - - - rs1392377 5:165816346 A - - - intergenic_variant - - - - - - rs2968363 5:165948469 C - - - intergenic_variant - - - - - - rs3096034 5:166065876 G - - - intergenic_variant - - - - - - rs959928 5:166432000 A ENSESTG00000008541 ENSESTT00000021478 Transcript intron_variant - - - - - - rs1159958 5:166630055 G - - - intergenic_variant - - - - - - rs13171830 5:166634359 G - - - intergenic_variant - - - - - - rs279410 5:167122331 G 57451 NM_001122679.1 Transcript intron_variant - - - - - - rs2617968 5:167525939 T ENSESTG00000009123 ENSESTT00000022913 Transcript intron_variant - - - - - - rs2617968 5:167525939 T ENSESTG00000009123 ENSESTT00000022917 Transcript intron_variant - - - - - - rs2617968 5:167525939 T ENSESTG00000009276 ENSESTT00000023251 Transcript intron_variant - - - - - - rs2617968 5:167525939 T 57451 NM_001122679.1 Transcript intron_variant - - - - - - rs2617968 5:167525939 T ENSESTG00000009123 ENSESTT00000022909 Transcript intron_variant - - - - - - rs297834 5:168572210 G 6586 NM_003062.2 Transcript intron_variant - - - - - - rs297834 5:168572210 G CCDS4369.1 CCDS4369.1 Transcript intron_variant - - - - - - rs297834 5:168572210 G ENSESTG00000030073 ENSESTT00000075698 Transcript intron_variant - - - - - - rs297866 5:168597887 G 6586 NM_003062.2 Transcript intron_variant - - - - - - rs297866 5:168597887 G CCDS4369.1 CCDS4369.1 Transcript intron_variant - - - - - - rs297866 5:168597887 G ENSESTG00000030073 ENSESTT00000075698 Transcript intron_variant - - - - - - rs297870 5:168602786 C 6586 NM_003062.2 Transcript intron_variant - - - - - - rs297870 5:168602786 C CCDS4369.1 CCDS4369.1 Transcript intron_variant - - - - - - rs297870 5:168602786 C ENSESTG00000030073 ENSESTT00000075698 Transcript intron_variant - - - - - - rs1363128 5:168613589 A 6586 NM_003062.2 Transcript intron_variant - - - - - - rs1363128 5:168613589 A CCDS4369.1 CCDS4369.1 Transcript intron_variant - - - - - - rs1363128 5:168613589 A ENSESTG00000030073 ENSESTT00000075698 Transcript intron_variant - - - - - - rs261075 5:169307261 G ENSESTG00000032566 ENSESTT00000082445 Transcript intron_variant - - - - - - rs261075 5:169307261 G ENSESTG00000032566 ENSESTT00000082455 Transcript intron_variant - - - - - - rs261075 5:169307261 G ENSESTG00000032566 ENSESTT00000082428 Transcript intron_variant - - - - - - rs261075 5:169307261 G 100131897 NM_001129891.1 Transcript intron_variant - - - - - - rs261075 5:169307261 G ENSESTG00000032746 ENSESTT00000082738 Transcript downstream_gene_variant - - - - - - DISTANCE=4086 rs261075 5:169307261 G 1794 NM_004946.2 Transcript intron_variant - - - - - - rs261075 5:169307261 G CCDS4371.1 CCDS4371.1 Transcript intron_variant - - - - - - rs261075 5:169307261 G CCDS47336.1 CCDS47336.1 Transcript intron_variant - - - - - - rs11741272 5:169528096 A CCDS47337.1 CCDS47337.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4866 rs11741272 5:169528096 A ENSESTG00000032670 ENSESTT00000082509 Transcript upstream_gene_variant - - - - - - DISTANCE=4818 rs11741272 5:169528096 A CCDS4372.1 CCDS4372.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4866 rs11741272 5:169528096 A 2299 NM_144769.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4821 rs11741272 5:169528096 A 2299 NM_012188.4 Transcript upstream_gene_variant - - - - - - DISTANCE=4821 rs10060749 5:169664761 C 133874 NM_001102609.1 Transcript intron_variant - - - - - - rs10060749 5:169664761 C ENSESTG00000032678 ENSESTT00000082565 Transcript intron_variant - - - - - - rs10060749 5:169664761 C ENSESTG00000032678 ENSESTT00000082589 Transcript intron_variant - - - - - - rs10060749 5:169664761 C ENSESTG00000032678 ENSESTT00000082579 Transcript intron_variant - - - - - - rs10060749 5:169664761 C CCDS47338.1 CCDS47338.1 Transcript intron_variant - - - - - - rs10060749 5:169664761 C ENSESTG00000032678 ENSESTT00000082548 Transcript intron_variant - - - - - - rs10060749 5:169664761 C ENSESTG00000032678 ENSESTT00000082598 Transcript intron_variant - - - - - - rs1973528 5:170114227 C 30820 NM_001034837.1 Transcript intron_variant - - - - - - rs1973528 5:170114227 C CCDS34285.1 CCDS34285.1 Transcript intron_variant - - - - - - rs1973528 5:170114227 C CCDS4374.1 CCDS4374.1 Transcript intron_variant - - - - - - rs1973528 5:170114227 C 30820 NM_001034838.1 Transcript intron_variant - - - - - - rs1973528 5:170114227 C 30820 NM_014592.2 Transcript intron_variant - - - - - - rs1973528 5:170114227 C CCDS34286.1 CCDS34286.1 Transcript intron_variant - - - - - - rs2216692 5:170246051 T 2568 NM_014211.2 Transcript downstream_gene_variant - - - - - - DISTANCE=5000 rs1200603 5:170694810 A ENSESTG00000001960 ENSESTT00000004914 Transcript intron_variant - - - - - - rs1200603 5:170694810 A CCDS34287.1 CCDS34287.1 Transcript intron_variant - - - - - - rs1200603 5:170694810 A 64901 NM_022897.3 Transcript intron_variant - - - - - - rs1200603 5:170694810 A ENSESTG00000001978 ENSESTT00000004927 Transcript intron_variant - - - - - - rs1200603 5:170694810 A ENSESTG00000001876 ENSESTT00000004684 Transcript intron_variant - - - - - - rs1200603 5:170694810 A ENSESTG00000001876 ENSESTT00000004687 Transcript intron_variant - - - - - - rs2964526 5:170697927 G ENSESTG00000001960 ENSESTT00000004914 Transcript intron_variant - - - - - - rs2964526 5:170697927 G CCDS34287.1 CCDS34287.1 Transcript intron_variant - - - - - - rs2964526 5:170697927 G 64901 NM_022897.3 Transcript intron_variant - - - - - - rs2964526 5:170697927 G ENSESTG00000001978 ENSESTT00000004927 Transcript intron_variant - - - - - - rs2964526 5:170697927 G ENSESTG00000001876 ENSESTT00000004684 Transcript intron_variant - - - - - - rs2964526 5:170697927 G ENSESTG00000001876 ENSESTT00000004687 Transcript intron_variant - - - - - - rs2964529 5:170749700 T ENSESTG00000001960 ENSESTT00000004914 Transcript intron_variant - - - - - - rs2964529 5:170749700 T ENSESTG00000001978 ENSESTT00000004927 Transcript intron_variant - - - - - - rs6872253 5:170803118 T - - - intergenic_variant - - - - - - rs4597987 5:170848981 C ENSESTG00000001937 ENSESTT00000004809 Transcript intron_variant - - - - - - rs4597987 5:170848981 C 8817 NM_003862.2 Transcript intron_variant - - - - - - rs4597987 5:170848981 C CCDS4378.1 CCDS4378.1 Transcript intron_variant - - - - - - rs1432964 5:170977593 C - - - intergenic_variant - - - - - - rs181947 5:171073458 G - - - intergenic_variant - - - - - - rs3097816 5:171156937 A 644994 XM_928062.6 Transcript intron_variant - - - - - - rs3101877 5:171156939 A 644994 XM_928062.6 Transcript intron_variant - - - - - - rs2060216 5:171369589 A ENSESTG00000032647 ENSESTT00000082433 Transcript intron_variant - - - - - - rs2060216 5:171369589 A CCDS47340.1 CCDS47340.1 Transcript intron_variant - - - - - - rs2060216 5:171369589 A 23291 NM_033645.2 Transcript intron_variant - - - - - - rs2060216 5:171369589 A 23291 NM_033644.2 Transcript intron_variant - - - - - - rs2060216 5:171369589 A ENSESTG00000032647 ENSESTT00000082412 Transcript intron_variant - - - - - - rs2060216 5:171369589 A CCDS47341.1 CCDS47341.1 Transcript intron_variant - - - - - - rs2060216 5:171369589 A 23291 NM_012300.2 Transcript intron_variant - - - - - - rs2060216 5:171369589 A CCDS34289.1 CCDS34289.1 Transcript intron_variant - - - - - - rs3131918 5:172621477 G - - - intergenic_variant - - - - - - rs6556067 5:172735875 C - - - intergenic_variant - - - - - - rs2546723 5:173131696 G ENSESTG00000034662 ENSESTT00000087611 Transcript intron_variant - - - - - - rs190503 5:173260240 C - ENSR00001416717 RegulatoryFeature regulatory_region_variant - - - - - - rs190503 5:173260240 C - - - intergenic_variant - - - - - - rs1032705 5:173734171 G - ENSR00001297284 RegulatoryFeature regulatory_region_variant - - - - - - rs1032705 5:173734171 G - - - intergenic_variant - - - - - - rs354972 5:173887121 G - - - intergenic_variant - - - - - - rs10075473 5:173997101 A ENSESTG00000022994 ENSESTT00000058019 Transcript intron_variant - - - - - - rs10075473 5:173997101 A ENSESTG00000022994 ENSESTT00000058029 Transcript intron_variant - - - - - - rs10075473 5:173997101 A ENSESTG00000022994 ENSESTT00000058045 Transcript intron_variant - - - - - - rs6556155 5:174134311 C - ENSR00001297349 RegulatoryFeature regulatory_region_variant - - - - - - rs6556155 5:174134311 C ENSESTG00000022994 ENSESTT00000058019 Transcript intron_variant - - - - - - rs6556155 5:174134311 C ENSESTG00000022994 ENSESTT00000058029 Transcript intron_variant - - - - - - rs6556155 5:174134311 C ENSESTG00000022994 ENSESTT00000058045 Transcript intron_variant - - - - - - rs1567204 5:174148498 G ENSESTG00000022905 ENSESTT00000057764 Transcript upstream_gene_variant - - - - - - DISTANCE=3110 rs1567204 5:174148498 G CCDS4392.1 CCDS4392.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3165 rs1567204 5:174148498 G ENSESTG00000022983 ENSESTT00000057993 Transcript downstream_gene_variant - - - - - - DISTANCE=3163 rs1567204 5:174148498 G 4488 NM_002449.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3077 rs1567204 5:174148498 G ENSESTG00000022983 ENSESTT00000057979 Transcript downstream_gene_variant - - - - - - DISTANCE=3165 rs1507802 5:174180419 T 100616202 NR_039777.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1629 rs11134873 5:174181005 C 100616202 NR_039777.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2215 rs1354568 5:174551084 T - - - intergenic_variant - - - - - - rs2112739 5:174577142 G - - - intergenic_variant - - - - - - rs622276 5:175059563 T - - - intergenic_variant - - - - - - rs1530879 5:175204387 C - - - intergenic_variant - - - - - - rs4444993 5:176012562 G ENSESTG00000011844 ENSESTT00000029709 Transcript upstream_gene_variant - - - - - - DISTANCE=1098 rs4444993 5:176012562 G 54825 NM_001171976.1 Transcript intron_variant - - - - - - rs4444993 5:176012562 G ENSESTG00000011844 ENSESTT00000029686 Transcript intron_variant - - - - - - rs4444993 5:176012562 G CCDS34297.1 CCDS34297.1 Transcript intron_variant - - - - - - rs4444993 5:176012562 G 54825 NM_017675.4 Transcript intron_variant - - - - - - rs4444993 5:176012562 G ENSESTG00000011844 ENSESTT00000029703 Transcript upstream_gene_variant - - - - - - DISTANCE=1090 rs4868666 5:176038435 G - ENSR00001416875 RegulatoryFeature regulatory_region_variant - - - - - - rs4868666 5:176038435 G ENSESTG00000012280 ENSESTT00000030814 Transcript upstream_gene_variant - - - - - - DISTANCE=1326 rs4868666 5:176038435 G ENSESTG00000012280 ENSESTT00000030811 Transcript upstream_gene_variant - - - - - - DISTANCE=1301 rs4868666 5:176038435 G 114787 NM_052899.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1304 rs244710 5:176545280 T - - - intergenic_variant - - - - - - rs10062787 5:177528195 C - - - intergenic_variant - - - - - - rs6601218 5:177570759 C ENSESTG00000019904 ENSESTT00000050119 Transcript intron_variant - - - - - - rs6601218 5:177570759 C CCDS4431.1 CCDS4431.1 Transcript intron_variant - - - - - - rs6601218 5:177570759 C ENSESTG00000019904 ENSESTT00000050131 Transcript intron_variant - - - - - - rs6601218 5:177570759 C ENSESTG00000019904 ENSESTT00000050159 Transcript upstream_gene_variant - - - - - - DISTANCE=26 rs6601218 5:177570759 C ENSESTG00000019904 ENSESTT00000050092 Transcript intron_variant - - - - - - rs6601218 5:177570759 C ENSESTG00000020309 ENSESTT00000050902 Transcript intron_variant - - - - - - rs6601218 5:177570759 C ENSESTG00000019904 ENSESTT00000050104 Transcript intron_variant - - - - - - rs6601218 5:177570759 C 64777 NM_022762.3 Transcript intron_variant - - - - - - rs6601218 5:177570759 C ENSESTG00000019904 ENSESTT00000050074 Transcript intron_variant - - - - - - rs6601218 5:177570759 C ENSESTG00000019904 ENSESTT00000050111 Transcript intron_variant - - - - - - rs6601218 5:177570759 C ENSESTG00000019904 ENSESTT00000050122 Transcript intron_variant - - - - - - rs7705458 5:177634401 C - ENSR00001298049 RegulatoryFeature regulatory_region_variant - - - - - - rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050732 Transcript downstream_gene_variant - - - - - - DISTANCE=1439 rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050713 Transcript downstream_gene_variant - - - - - - DISTANCE=1439 rs7705458 5:177634401 C ENSESTG00000020022 ENSESTT00000050278 Transcript intron_variant - - - - - - rs7705458 5:177634401 C ENSESTG00000020022 ENSESTT00000050320 Transcript intron_variant - - - - - - rs7705458 5:177634401 C ENSESTG00000020022 ENSESTT00000050338 Transcript intron_variant - - - - - - rs7705458 5:177634401 C ENSESTG00000020022 ENSESTT00000050315 Transcript intron_variant - - - - - - rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050743 Transcript downstream_gene_variant - - - - - - DISTANCE=1185 rs7705458 5:177634401 C ENSESTG00000020022 ENSESTT00000050299 Transcript intron_variant - - - - - - rs7705458 5:177634401 C 3182 NM_004499.3 Transcript intron_variant - - - - - - rs7705458 5:177634401 C ENSESTG00000020022 ENSESTT00000050343 Transcript intron_variant - - - - - - rs7705458 5:177634401 C 3182 NM_031266.2 Transcript intron_variant - - - - - - rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050670 Transcript downstream_gene_variant - - - - - - DISTANCE=1185 rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050767 Transcript downstream_gene_variant - - - - - - DISTANCE=1185 rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050722 Transcript downstream_gene_variant - - - - - - DISTANCE=1185 rs7705458 5:177634401 C CCDS34309.1 CCDS34309.1 Transcript intron_variant - - - - - - rs7705458 5:177634401 C 85007 NM_153373.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1139 rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050766 Transcript downstream_gene_variant - - - - - - DISTANCE=1185 rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050744 Transcript downstream_gene_variant - - - - - - DISTANCE=1439 rs7705458 5:177634401 C CCDS4434.1 CCDS4434.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4521 rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050730 Transcript downstream_gene_variant - - - - - - DISTANCE=1185 rs7705458 5:177634401 C ENSESTG00000020161 ENSESTT00000050642 Transcript downstream_gene_variant - - - - - - DISTANCE=1185 rs7705458 5:177634401 C CCDS34310.1 CCDS34310.1 Transcript intron_variant - - - - - - rs252073 5:178618219 G 9509 NM_014244.4 Transcript intron_variant - - - - - - rs252073 5:178618219 G ENSESTG00000025866 ENSESTT00000065210 Transcript intron_variant - - - - - - rs252073 5:178618219 G CCDS34311.1 CCDS34311.1 Transcript intron_variant - - - - - - rs252073 5:178618219 G CCDS4444.1 CCDS4444.1 Transcript intron_variant - - - - - - rs252073 5:178618219 G 9509 NM_021599.2 Transcript intron_variant - - - - - - rs30383 5:179295414 C 23061 NM_198868.2 Transcript intron_variant - - - - - - rs30383 5:179295414 C ENSESTG00000006384 ENSESTT00000016204 Transcript intron_variant - - - - - - rs30383 5:179295414 C ENSESTG00000006384 ENSESTT00000016193 Transcript intron_variant - - - - - - rs30383 5:179295414 C ENSESTG00000006384 ENSESTT00000016182 Transcript intron_variant - - - - - - rs30383 5:179295414 C ENSESTG00000006250 ENSESTT00000015758 Transcript downstream_gene_variant - - - - - - DISTANCE=398 rs30383 5:179295414 C CCDS43408.1 CCDS43408.1 Transcript intron_variant - - - - - - rs30383 5:179295414 C 23061 NM_015043.3 Transcript intron_variant - - - - - - rs30383 5:179295414 C CCDS4450.1 CCDS4450.1 Transcript intron_variant - - - - - - rs7737102 5:179576368 C 255426 NM_175062.3 Transcript intron_variant - - - - - - rs7737102 5:179576368 C ENSESTG00000006332 ENSESTT00000015994 Transcript intron_variant - - - - - - rs4700895 5:179601392 G - ENSR00001298405 RegulatoryFeature regulatory_region_variant - - - - - - rs4700895 5:179601392 G 255426 NM_175062.3 Transcript intron_variant - - - - - - rs4700895 5:179601392 G ENSESTG00000006332 ENSESTT00000015994 Transcript intron_variant - - - - - - rs10077348 5:179688316 A 5601 NM_001135044.1 Transcript intron_variant - - - - - - rs10077348 5:179688316 A CCDS4454.1 CCDS4454.1 Transcript intron_variant - - - - - - rs10077348 5:179688316 A 5601 NM_002752.4 Transcript intron_variant - - - - - - rs10077348 5:179688316 A 5601 NM_139068.2 Transcript intron_variant - - - - - - rs10077348 5:179688316 A CCDS43410.1 CCDS43410.1 Transcript intron_variant - - - - - - rs10077348 5:179688316 A CCDS4453.1 CCDS4453.1 Transcript intron_variant - - - - - - rs10077348 5:179688316 A 5601 NM_139070.2 Transcript intron_variant - - - - - - rs10077348 5:179688316 A ENSESTG00000006311 ENSESTT00000015947 Transcript intron_variant - - - - - - rs10077348 5:179688316 A CCDS43409.1 CCDS43409.1 Transcript intron_variant - - - - - - rs10077348 5:179688316 A CCDS47356.1 CCDS47356.1 Transcript intron_variant - - - - - - rs10077348 5:179688316 A 5601 NM_139069.2 Transcript intron_variant - - - - - - rs10077348 5:179688316 A ENSESTG00000006311 ENSESTT00000015929 Transcript intron_variant - - - - - - rs593669 5:180206123 T - - - intergenic_variant - - - - - - rs254445 5:180666706 T - ENSR00001298645 RegulatoryFeature regulatory_region_variant - - - - - - rs254445 5:180666706 T ENSESTG00000010501 ENSESTT00000026347 Transcript intron_variant - - - - - - rs254445 5:180666706 T ENSESTG00000010449 ENSESTT00000026173 Transcript upstream_gene_variant - - - - - - DISTANCE=1652 rs254445 5:180666706 T ENSESTG00000010537 ENSESTT00000026357 Transcript upstream_gene_variant - - - - - - DISTANCE=3898 rs254445 5:180666706 T 90933 NR_045218.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3898 rs254445 5:180666706 T 619570 NR_002591.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3608 rs254445 5:180666706 T 10399 NM_006098.4 Transcript intron_variant - - - - - - rs254445 5:180666706 T 619571 NR_002592.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2112 rs254445 5:180666706 T 90933 NM_201627.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3898 rs254445 5:180666706 T CCDS4466.1 CCDS4466.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4931 rs254445 5:180666706 T CCDS34324.1 CCDS34324.1 Transcript intron_variant - - - - - - rs254445 5:180666706 T ENSESTG00000010501 ENSESTT00000026336 Transcript intron_variant - - - - - - rs254445 5:180666706 T ENSESTG00000010501 ENSESTT00000026322 Transcript intron_variant - - - - - - rs254445 5:180666706 T 90933 NM_033549.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3898 rs254445 5:180666706 T ENSESTG00000010542 ENSESTT00000026365 Transcript upstream_gene_variant - - - - - - DISTANCE=4922 rs254445 5:180666706 T CCDS4465.1 CCDS4465.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4327 rs2316514 6:410826 C - ENSR00001208548 RegulatoryFeature regulatory_region_variant - - - - - - rs2316514 6:410826 C 3662 NM_002460.3 Transcript 3_prime_UTR_variant 4710 - - - - - rs2316514 6:410826 C 3662 NR_046000.1 Transcript non_coding_exon_variant,nc_transcript_variant 4841 - - - - - rs2316514 6:410826 C 3662 NM_001195286.1 Transcript 3_prime_UTR_variant 4707 - - - - - rs2316514 6:410826 C CCDS4469.1 CCDS4469.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3228 rs4298383 6:456893 G - - - intergenic_variant - - - - - - rs4959476 6:885418 C - ENSR00001492384 RegulatoryFeature regulatory_region_variant - - - - - - rs4959476 6:885418 C - - - intergenic_variant - - - - - - rs240672 6:1042536 T 285768 NR_027116.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs240672 6:1042536 T 285768 NR_027115.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs2745633 6:1441424 C - - - intergenic_variant - - - - - - rs6906669 6:2107440 G ENSESTG00000033674 ENSESTT00000085169 Transcript intron_variant - - - - - - rs6906669 6:2107440 G 2762 NM_001500.3 Transcript intron_variant - - - - - - rs6906669 6:2107440 G CCDS58994.1 CCDS58994.1 Transcript intron_variant - - - - - - rs6906669 6:2107440 G CCDS4474.1 CCDS4474.1 Transcript intron_variant - - - - - - rs6906669 6:2107440 G 2762 NM_001253846.1 Transcript intron_variant - - - - - - rs1254738 6:2518003 G - - - intergenic_variant - - - - - - rs1680827 6:2573298 A - - - intergenic_variant - - - - - - rs4959198 6:2654413 A - - - intergenic_variant - - - - - - rs410362 6:2861937 G - ENSR00001209101 RegulatoryFeature regulatory_region_variant - - - - - - rs410362 6:2861937 G ENSESTG00000026427 ENSESTT00000066584 Transcript intron_variant - - - - - - rs410362 6:2861937 G ENSESTG00000026427 ENSESTT00000066566 Transcript intron_variant - - - - - - rs410362 6:2861937 G 221756 NR_033851.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs795215 6:4360976 A - - - intergenic_variant - - - - - - rs430741 6:4365573 C - - - intergenic_variant - - - - - - rs4960030 6:4703609 G 9425 NR_026590.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2784 rs1933226 6:4743536 T - ENSR00001209673 RegulatoryFeature regulatory_region_variant - - - - - - rs1933226 6:4743536 T 9425 NR_026590.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6921792 6:4744019 T 9425 NR_026590.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs947152 6:5029083 G ENSESTG00000019050 ENSESTT00000047896 Transcript upstream_gene_variant - - - - - - DISTANCE=1192 rs584962 6:5086211 C - ENSR00001209766 RegulatoryFeature regulatory_region_variant - - - - - - rs584962 6:5086211 C ENSESTG00000019108 ENSESTT00000048071 Transcript intron_variant - - - - - - rs584962 6:5086211 C CCDS47366.1 CCDS47366.1 Transcript synonymous_variant 492 492 164 L ctG/ctC - rs584962 6:5086211 C 648791 NM_001145115.1 Transcript synonymous_variant 492 492 164 L ctG/ctC - rs584962 6:5086211 C ENSESTG00000019108 ENSESTT00000048083 Transcript intron_variant - - - - - - rs463054 6:5139012 A ENSESTG00000019108 ENSESTT00000048071 Transcript intron_variant - - - - - - rs463054 6:5139012 A ENSESTG00000019108 ENSESTT00000048121 Transcript intron_variant - - - - - - rs463054 6:5139012 A 57128 NM_001164841.1 Transcript intron_variant - - - - - - rs463054 6:5139012 A ENSESTG00000019108 ENSESTT00000048116 Transcript intron_variant - - - - - - rs463054 6:5139012 A ENSESTG00000019108 ENSESTT00000048142 Transcript intron_variant - - - - - - rs463054 6:5139012 A CCDS4493.1 CCDS4493.1 Transcript intron_variant - - - - - - rs463054 6:5139012 A 57128 NM_020408.4 Transcript intron_variant - - - - - - rs463054 6:5139012 A ENSESTG00000019108 ENSESTT00000048083 Transcript intron_variant - - - - - - rs913909 6:5212146 C CCDS54962.1 CCDS54962.1 Transcript intron_variant - - - - - - rs913909 6:5212146 C ENSESTG00000019108 ENSESTT00000048071 Transcript intron_variant - - - - - - rs913909 6:5212146 C ENSESTG00000019108 ENSESTT00000048121 Transcript intron_variant - - - - - - rs913909 6:5212146 C 57128 NM_001164841.1 Transcript intron_variant - - - - - - rs913909 6:5212146 C 57128 NM_001164840.1 Transcript intron_variant - - - - - - rs913909 6:5212146 C ENSESTG00000019108 ENSESTT00000048116 Transcript intron_variant - - - - - - rs913909 6:5212146 C ENSESTG00000019108 ENSESTT00000048142 Transcript intron_variant - - - - - - rs913909 6:5212146 C ENSESTG00000019108 ENSESTT00000048126 Transcript intron_variant - - - - - - rs913909 6:5212146 C CCDS54961.1 CCDS54961.1 Transcript intron_variant - - - - - - rs913909 6:5212146 C CCDS4493.1 CCDS4493.1 Transcript intron_variant - - - - - - rs913909 6:5212146 C 57128 NM_020408.4 Transcript intron_variant - - - - - - rs913909 6:5212146 C ENSESTG00000019108 ENSESTT00000048083 Transcript intron_variant - - - - - - rs4959335 6:5214626 C CCDS54962.1 CCDS54962.1 Transcript intron_variant - - - - - - rs4959335 6:5214626 C ENSESTG00000019108 ENSESTT00000048071 Transcript intron_variant - - - - - - rs4959335 6:5214626 C ENSESTG00000019108 ENSESTT00000048121 Transcript intron_variant - - - - - - rs4959335 6:5214626 C 57128 NM_001164841.1 Transcript intron_variant - - - - - - rs4959335 6:5214626 C 57128 NM_001164840.1 Transcript intron_variant - - - - - - rs4959335 6:5214626 C ENSESTG00000019108 ENSESTT00000048116 Transcript intron_variant - - - - - - rs4959335 6:5214626 C ENSESTG00000019108 ENSESTT00000048142 Transcript intron_variant - - - - - - rs4959335 6:5214626 C ENSESTG00000019108 ENSESTT00000048126 Transcript intron_variant - - - - - - rs4959335 6:5214626 C CCDS54961.1 CCDS54961.1 Transcript intron_variant - - - - - - rs4959335 6:5214626 C CCDS4493.1 CCDS4493.1 Transcript intron_variant - - - - - - rs4959335 6:5214626 C 57128 NM_020408.4 Transcript intron_variant - - - - - - rs4959335 6:5214626 C ENSESTG00000019108 ENSESTT00000048083 Transcript intron_variant - - - - - - rs1534894 6:5524246 C 10667 NM_006567.3 Transcript intron_variant - - - - - - rs1534894 6:5524246 C CCDS4494.1 CCDS4494.1 Transcript intron_variant - - - - - - rs1534894 6:5524246 C ENSESTG00000019056 ENSESTT00000047974 Transcript intron_variant - - - - - - rs6597143 6:5564152 T ENSESTG00000019056 ENSESTT00000047989 Transcript intron_variant - - - - - - rs6597143 6:5564152 T 10667 NM_006567.3 Transcript intron_variant - - - - - - rs6597143 6:5564152 T CCDS4494.1 CCDS4494.1 Transcript intron_variant - - - - - - rs6597143 6:5564152 T ENSESTG00000019056 ENSESTT00000047974 Transcript intron_variant - - - - - - rs6597152 6:5625742 G 10667 NM_006567.3 Transcript intron_variant - - - - - - rs6597152 6:5625742 G CCDS4494.1 CCDS4494.1 Transcript intron_variant - - - - - - rs6597152 6:5625742 G ENSESTG00000019056 ENSESTT00000047974 Transcript intron_variant - - - - - - rs4960118 6:5632100 T 10667 NM_006567.3 Transcript intron_variant - - - - - - rs4960118 6:5632100 T CCDS4494.1 CCDS4494.1 Transcript intron_variant - - - - - - rs4960118 6:5632100 T ENSESTG00000019056 ENSESTT00000047974 Transcript intron_variant - - - - - - rs4959346 6:5671032 C - ENSR00001209887 RegulatoryFeature regulatory_region_variant - - - - - - rs4959346 6:5671032 C 10667 NM_006567.3 Transcript intron_variant - - - - - - rs4959346 6:5671032 C CCDS4494.1 CCDS4494.1 Transcript intron_variant - - - - - - rs4959346 6:5671032 C ENSESTG00000019056 ENSESTT00000047974 Transcript intron_variant - - - - - - rs912024 6:5949062 C ENSESTG00000019090 ENSESTT00000048006 Transcript intron_variant - - - - - - rs528372 6:6575219 T ENSESTG00000032167 ENSESTT00000081154 Transcript intron_variant - - - - - - rs528372 6:6575219 T 285780 NR_026970.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2765362 6:6966738 A - - - intergenic_variant - - - - - - rs1614537 6:7034589 T - - - intergenic_variant - - - - - - rs562701 6:7161831 C 6239 NM_001003698.3 Transcript intron_variant - - - - - - rs562701 6:7161831 C 6239 NM_001003700.1 Transcript intron_variant - - - - - - rs562701 6:7161831 C 6239 NM_001003699.3 Transcript intron_variant - - - - - - rs562701 6:7161831 C ENSESTG00000009370 ENSESTT00000023488 Transcript intron_variant - - - - - - rs562701 6:7161831 C ENSESTG00000009370 ENSESTT00000023509 Transcript intron_variant - - - - - - rs562701 6:7161831 C 6239 NM_001168344.1 Transcript intron_variant - - - - - - rs562701 6:7161831 C ENSESTG00000009370 ENSESTT00000023492 Transcript intron_variant - - - - - - rs562701 6:7161831 C ENSESTG00000009370 ENSESTT00000023503 Transcript intron_variant - - - - - - rs2764088 6:7287513 T ENSESTG00000009621 ENSESTT00000024151 Transcript intron_variant - - - - - - rs2764088 6:7287513 T 6745 NM_003144.3 Transcript 3_prime_UTR_variant 3633 - - - - - rs2764088 6:7287513 T ENSESTG00000009403 ENSESTT00000023568 Transcript intron_variant - - - - - - rs2764088 6:7287513 T CCDS4499.1 CCDS4499.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2584 rs2764088 6:7287513 T ENSESTG00000009643 ENSESTT00000024157 Transcript intron_variant - - - - - - rs2147704 6:7348335 C CCDS54965.1 CCDS54965.1 Transcript intron_variant - - - - - - rs2147704 6:7348335 C 285782 NM_001170693.1 Transcript intron_variant - - - - - - rs2147704 6:7348335 C CCDS54964.1 CCDS54964.1 Transcript intron_variant - - - - - - rs2147704 6:7348335 C 285782 NM_205864.2 Transcript intron_variant - - - - - - rs2147704 6:7348335 C ENSESTG00000009616 ENSESTT00000024102 Transcript intron_variant - - - - - - rs2147704 6:7348335 C CCDS47367.1 CCDS47367.1 Transcript intron_variant - - - - - - rs2147704 6:7348335 C 285782 NM_001170692.1 Transcript intron_variant - - - - - - rs2806234 6:7563983 G CCDS4501.1 CCDS4501.1 Transcript synonymous_variant 741 741 247 A gcT/gcG - rs2806234 6:7563983 G ENSESTG00000009483 ENSESTT00000023833 Transcript 5_prime_UTR_variant 70 - - - - - rs2806234 6:7563983 G 1832 NM_001008844.1 Transcript synonymous_variant 1020 741 247 A gcT/gcG - rs2806234 6:7563983 G 1832 NM_004415.2 Transcript synonymous_variant 1020 741 247 A gcT/gcG - rs2806234 6:7563983 G ENSESTG00000009609 ENSESTT00000024088 Transcript intron_variant - - - - - - rs2806234 6:7563983 G CCDS47368.1 CCDS47368.1 Transcript synonymous_variant 741 741 247 A gcT/gcG - rs2806234 6:7563983 G ENSESTG00000009483 ENSESTT00000023747 Transcript synonymous_variant 259 159 53 A gcT/gcG - rs2806234 6:7563983 G ENSESTG00000009483 ENSESTT00000023785 Transcript 5_prime_UTR_variant 70 - - - - - rs270384 6:7774400 C 654 NM_001718.4 Transcript intron_variant - - - - - - rs270384 6:7774400 C CCDS4503.1 CCDS4503.1 Transcript intron_variant - - - - - - rs270384 6:7774400 C ENSESTG00000009539 ENSESTT00000023934 Transcript intron_variant - - - - - - rs2210730 6:8107615 G 9521 NM_001135650.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4787 rs2210730 6:8107615 G ENSESTG00000026946 ENSESTT00000067934 Transcript upstream_gene_variant - - - - - - DISTANCE=4836 rs2210730 6:8107615 G 9521 NM_004280.4 Transcript upstream_gene_variant - - - - - - DISTANCE=4787 rs2210730 6:8107615 G ENSESTG00000026946 ENSESTT00000067963 Transcript upstream_gene_variant - - - - - - DISTANCE=4901 rs2210730 6:8107615 G ENSESTG00000026946 ENSESTT00000067999 Transcript upstream_gene_variant - - - - - - DISTANCE=4910 rs2210730 6:8107615 G CCDS47370.1 CCDS47370.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4861 rs2210730 6:8107615 G CCDS4507.1 CCDS4507.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4861 rs2210730 6:8107615 G 100526837 NR_037618.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4787 rs2210730 6:8107615 G ENSESTG00000026946 ENSESTT00000067954 Transcript upstream_gene_variant - - - - - - DISTANCE=4867 rs2210730 6:8107615 G ENSESTG00000026946 ENSESTT00000067920 Transcript upstream_gene_variant - - - - - - DISTANCE=4834 rs1414343 6:8467605 A 100506207 NR_038979.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1414343 6:8467605 A 100506207 NR_038980.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4960455 6:8752893 G 100506207 NR_038980.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs35684683 6:9214354 G - - - intergenic_variant - - - - - - rs6927482 6:9339985 G - - - intergenic_variant - - - - - - rs912884 6:9935704 C 266553 XM_003118558.2 Transcript intron_variant - - - - - - rs1156521 6:10194330 T - - - intergenic_variant - - - - - - rs644619 6:10470975 G - - - intergenic_variant - - - - - - rs6906408 6:10853137 C ENSESTG00000013271 ENSESTT00000033301 Transcript intron_variant - - - - - - rs4363034 6:11395826 G - - - intergenic_variant - - - - - - rs4711517 6:12003546 G ENSESTG00000008436 ENSESTT00000021266 Transcript upstream_gene_variant - - - - - - DISTANCE=2069 rs4711517 6:12003546 G ENSESTG00000008190 ENSESTT00000020694 Transcript upstream_gene_variant - - - - - - DISTANCE=4571 rs6900196 6:12122645 G 3096 NM_002114.2 Transcript missense_variant 2796 2617 873 T/A Act/Gct - PolyPhen=benign;SIFT=tolerated rs6900196 6:12122645 G CCDS43426.1 CCDS43426.1 Transcript missense_variant 2617 2617 873 T/A Act/Gct - PolyPhen=benign;SIFT=tolerated rs6900196 6:12122645 G ENSESTG00000008204 ENSESTT00000020738 Transcript upstream_gene_variant - - - - - - DISTANCE=2864 rs6900196 6:12122645 G ENSESTG00000008199 ENSESTT00000020711 Transcript downstream_gene_variant - - - - - - DISTANCE=2190 rs6900196 6:12122645 G ENSESTG00000008199 ENSESTT00000020721 Transcript downstream_gene_variant - - - - - - DISTANCE=2332 rs6900196 6:12122645 G ENSESTG00000008199 ENSESTT00000020717 Transcript downstream_gene_variant - - - - - - DISTANCE=2232 rs220013 6:12253040 G - - - intergenic_variant - - - - - - rs220014 6:12266734 C - - - intergenic_variant - - - - - - rs220015 6:12268592 C - - - intergenic_variant - - - - - - rs531466 6:12723922 T 221692 NM_030948.2 Transcript intron_variant - - - - - - rs531466 6:12723922 T ENSESTG00000008359 ENSESTT00000021129 Transcript intron_variant - - - - - - rs531466 6:12723922 T 221692 NM_001242648.1 Transcript intron_variant - - - - - - rs531466 6:12723922 T ENSESTG00000008359 ENSESTT00000021131 Transcript intron_variant - - - - - - rs531466 6:12723922 T ENSESTG00000008359 ENSESTT00000021113 Transcript intron_variant - - - - - - rs1571995 6:12812812 G 221692 NM_030948.2 Transcript intron_variant - - - - - - rs1571995 6:12812812 G 221692 NM_001242648.1 Transcript intron_variant - - - - - - rs1571995 6:12812812 G ENSESTG00000008359 ENSESTT00000021131 Transcript intron_variant - - - - - - rs1024165 6:13226483 A - ENSR00001211368 RegulatoryFeature regulatory_region_variant - - - - - - rs1024165 6:13226483 A ENSESTG00000020207 ENSESTT00000050701 Transcript intron_variant - - - - - - rs1024165 6:13226483 A 221692 NM_030948.2 Transcript intron_variant - - - - - - rs1024165 6:13226483 A 221692 NM_001242648.1 Transcript intron_variant - - - - - - rs28491226 6:13815695 T - ENSR00001211558 RegulatoryFeature regulatory_region_variant - - - - - - rs28491226 6:13815695 T CCDS35495.1 CCDS35495.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1034 rs28491226 6:13815695 T 63933 NM_001031713.3 Transcript upstream_gene_variant - - - - - - DISTANCE=903 rs28491226 6:13815695 T ENSESTG00000020919 ENSESTT00000052632 Transcript upstream_gene_variant - - - - - - DISTANCE=1069 rs28491226 6:13815695 T ENSESTG00000020919 ENSESTT00000052542 Transcript upstream_gene_variant - - - - - - DISTANCE=1069 rs28491226 6:13815695 T ENSESTG00000020919 ENSESTT00000052636 Transcript upstream_gene_variant - - - - - - DISTANCE=1069 rs863272 6:14635004 G - - - intergenic_variant - - - - - - rs9349964 6:15025854 A - - - intergenic_variant - - - - - - rs2791607 6:15117966 C - - - intergenic_variant - - - - - - rs808206 6:15344221 G - ENSR00001211998 RegulatoryFeature regulatory_region_variant - - - - - - rs808206 6:15344221 G ENSESTG00000007765 ENSESTT00000019629 Transcript intron_variant - - - - - - rs808206 6:15344221 G ENSESTG00000007765 ENSESTT00000019669 Transcript intron_variant - - - - - - rs808206 6:15344221 G ENSESTG00000007765 ENSESTT00000019640 Transcript intron_variant - - - - - - rs808206 6:15344221 G CCDS4533.1 CCDS4533.1 Transcript intron_variant - - - - - - rs808206 6:15344221 G 3720 NM_004973.3 Transcript intron_variant - - - - - - rs808206 6:15344221 G 3720 NM_001267040.1 Transcript intron_variant - - - - - - rs808206 6:15344221 G ENSESTG00000007765 ENSESTT00000019650 Transcript intron_variant - - - - - - rs808206 6:15344221 G ENSESTG00000007765 ENSESTT00000019671 Transcript intron_variant - - - - - - rs808206 6:15344221 G ENSESTG00000007765 ENSESTT00000019665 Transcript intron_variant - - - - - - rs808206 6:15344221 G ENSESTG00000007765 ENSESTT00000019661 Transcript intron_variant - - - - - - rs707837 6:15351901 T - ENSR00001211999 RegulatoryFeature regulatory_region_variant - - - - - - rs707837 6:15351901 T ENSESTG00000007765 ENSESTT00000019629 Transcript intron_variant - - - - - - rs707837 6:15351901 T ENSESTG00000007765 ENSESTT00000019669 Transcript intron_variant - - - - - - rs707837 6:15351901 T ENSESTG00000007765 ENSESTT00000019640 Transcript intron_variant - - - - - - rs707837 6:15351901 T CCDS4533.1 CCDS4533.1 Transcript intron_variant - - - - - - rs707837 6:15351901 T 3720 NM_004973.3 Transcript intron_variant - - - - - - rs707837 6:15351901 T 3720 NM_001267040.1 Transcript intron_variant - - - - - - rs707837 6:15351901 T ENSESTG00000007765 ENSESTT00000019650 Transcript intron_variant - - - - - - rs707837 6:15351901 T ENSESTG00000007765 ENSESTT00000019671 Transcript intron_variant - - - - - - rs707837 6:15351901 T ENSESTG00000007765 ENSESTT00000019665 Transcript intron_variant - - - - - - rs707837 6:15351901 T ENSESTG00000007765 ENSESTT00000019661 Transcript intron_variant - - - - - - rs9477290 6:17015522 T - ENSR00001212497 RegulatoryFeature regulatory_region_variant - - - - - - rs9477290 6:17015522 T - - - intergenic_variant - - - - - - rs1322032 6:17042724 T - - - intergenic_variant - - - - - - rs7755909 6:17055829 C - - - intergenic_variant - - - - - - rs9396798 6:17729533 G - ENSR00001212625 RegulatoryFeature regulatory_region_variant - - - - - - rs9396798 6:17729533 G - - - intergenic_variant - - - - - - rs9383430 6:18691240 A - - - intergenic_variant - - - - - - rs973801 6:19037741 C ENSESTG00000005454 ENSESTT00000013866 Transcript intron_variant - - - - - - rs9348415 6:20191340 A ENSESTG00000029583 ENSESTT00000074511 Transcript intron_variant - - - - - - rs9348415 6:20191340 A CCDS34346.1 CCDS34346.1 Transcript intron_variant - - - - - - rs9348415 6:20191340 A 154141 NM_001080480.1 Transcript intron_variant - - - - - - rs9348415 6:20191340 A ENSESTG00000029583 ENSESTT00000074445 Transcript intron_variant - - - - - - rs4712486 6:20319851 T - ENSR00001213000 RegulatoryFeature regulatory_region_variant - - - - - - rs4712486 6:20319851 T - - - intergenic_variant - - - - - - rs9350259 6:20566301 C CCDS4546.1 CCDS4546.1 Transcript intron_variant - - - - - - rs9350259 6:20566301 C 54901 NM_017774.3 Transcript intron_variant - - - - - - rs9350259 6:20566301 C ENSESTG00000029269 ENSESTT00000073740 Transcript intron_variant - - - - - - rs9350259 6:20566301 C ENSESTG00000029269 ENSESTT00000073771 Transcript intron_variant - - - - - - rs9350277 6:20741741 A ENSESTG00000029353 ENSESTT00000074013 Transcript intron_variant - - - - - - rs9350277 6:20741741 A CCDS4546.1 CCDS4546.1 Transcript intron_variant - - - - - - rs9350277 6:20741741 A ENSESTG00000029353 ENSESTT00000074030 Transcript intron_variant - - - - - - rs9350277 6:20741741 A 54901 NM_017774.3 Transcript intron_variant - - - - - - rs2493868 6:21183878 G CCDS4546.1 CCDS4546.1 Transcript intron_variant - - - - - - rs2493868 6:21183878 G 54901 NM_017774.3 Transcript intron_variant - - - - - - rs2493868 6:21183878 G ENSESTG00000004188 ENSESTT00000010567 Transcript intron_variant - - - - - - rs9368289 6:21227752 G - ENSR00001493900 RegulatoryFeature regulatory_region_variant - - - - - - rs9368289 6:21227752 G CCDS4546.1 CCDS4546.1 Transcript intron_variant - - - - - - rs9368289 6:21227752 G 54901 NM_017774.3 Transcript intron_variant - - - - - - rs9368289 6:21227752 G ENSESTG00000004188 ENSESTT00000010567 Transcript intron_variant - - - - - - rs9368289 6:21227752 G ENSESTG00000004188 ENSESTT00000010571 Transcript intron_variant - - - - - - rs6456434 6:21541964 T - - - intergenic_variant - - - - - - rs1534886 6:22106455 G ENSESTG00000013812 ENSESTT00000034523 Transcript intron_variant - - - - - - rs1534886 6:22106455 G ENSESTG00000013812 ENSESTT00000034528 Transcript intron_variant - - - - - - rs1534886 6:22106455 G 401237 NR_015410.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4236009 6:22148811 G - ENSR00001493987 RegulatoryFeature regulatory_region_variant - - - - - - rs4236009 6:22148811 G ENSESTG00000013812 ENSESTT00000034523 Transcript intron_variant - - - - - - rs4236009 6:22148811 G ENSESTG00000013812 ENSESTT00000034528 Transcript intron_variant - - - - - - rs4236009 6:22148811 G 729177 NR_034143.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1389 rs4236009 6:22148811 G ENSESTG00000013855 ENSESTT00000034612 Transcript upstream_gene_variant - - - - - - DISTANCE=1389 rs4236009 6:22148811 G 401237 NR_015410.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1205949 6:22319848 A - - - intergenic_variant - - - - - - rs2143421 6:22665791 G ENSESTG00000013826 ENSESTT00000034545 Transcript downstream_gene_variant - - - - - - DISTANCE=137 rs2143421 6:22665791 G ENSESTG00000013829 ENSESTT00000034553 Transcript intron_variant - - - - - - rs6928567 6:22667946 G ENSESTG00000013826 ENSESTT00000034545 Transcript downstream_gene_variant - - - - - - DISTANCE=2292 rs6928567 6:22667946 G ENSESTG00000013829 ENSESTT00000034553 Transcript intron_variant - - - - - - rs1205507 6:22848356 A - - - intergenic_variant - - - - - - rs1925438 6:23315186 C - - - intergenic_variant - - - - - - rs4711047 6:23343048 G ENSESTG00000014031 ENSESTT00000035074 Transcript intron_variant - - - - - - rs4711047 6:23343048 G ENSESTG00000014031 ENSESTT00000035080 Transcript intron_variant - - - - - - rs197957 6:23574815 G - - - intergenic_variant - - - - - - rs496063 6:23685674 T - - - intergenic_variant - - - - - - rs6939669 6:23754083 C - - - intergenic_variant - - - - - - rs791759 6:23860259 G - - - intergenic_variant - - - - - - rs6923150 6:23901640 T - - - intergenic_variant - - - - - - rs4236030 6:24173273 G CCDS4550.1 CCDS4550.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1685 rs4236030 6:24173273 G ENSESTG00000035364 ENSESTT00000089305 Transcript downstream_gene_variant - - - - - - DISTANCE=1533 rs4236030 6:24173273 G 51473 NM_001195610.1 Transcript 3_prime_UTR_variant 3325 - - - - - rs4236030 6:24173273 G ENSESTG00000035364 ENSESTT00000089304 Transcript downstream_gene_variant - - - - - - DISTANCE=1533 rs4236030 6:24173273 G 51473 NM_016356.3 Transcript 3_prime_UTR_variant 3418 - - - - - rs4490654 6:24189448 A CCDS4550.1 CCDS4550.1 Transcript intron_variant - - - - - - rs4490654 6:24189448 A ENSESTG00000035364 ENSESTT00000089305 Transcript intron_variant - - - - - - rs4490654 6:24189448 A 51473 NM_001195610.1 Transcript intron_variant - - - - - - rs4490654 6:24189448 A ENSESTG00000035364 ENSESTT00000089304 Transcript intron_variant - - - - - - rs4490654 6:24189448 A 51473 NM_016356.3 Transcript intron_variant - - - - - - rs6456600 6:24206090 T CCDS4550.1 CCDS4550.1 Transcript intron_variant - - - - - - rs6456600 6:24206090 T ENSESTG00000035364 ENSESTT00000089305 Transcript intron_variant - - - - - - rs6456600 6:24206090 T 51473 NM_001195610.1 Transcript intron_variant - - - - - - rs6456600 6:24206090 T ENSESTG00000035364 ENSESTT00000089304 Transcript intron_variant - - - - - - rs6456600 6:24206090 T 51473 NM_016356.3 Transcript intron_variant - - - - - - rs812093 6:24362076 G CCDS4550.1 CCDS4550.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4098 rs812093 6:24362076 G 51473 NM_001195610.1 Transcript intron_variant - - - - - - rs812093 6:24362076 G CCDS4551.1 CCDS4551.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3954 rs812093 6:24362076 G ENSESTG00000035364 ENSESTT00000089304 Transcript upstream_gene_variant - - - - - - DISTANCE=3909 rs812093 6:24362076 G 51473 NM_016356.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3796 rs812093 6:24362076 G 353219 NM_181337.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3564 rs4577791 6:25387369 A 55604 NM_017640.5 Transcript intron_variant - - - - - - rs4577791 6:25387369 A ENSESTG00000029308 ENSESTT00000073783 Transcript intron_variant - - - - - - rs4577791 6:25387369 A ENSESTG00000029620 ENSESTT00000074541 Transcript intron_variant - - - - - - rs4577791 6:25387369 A 55604 NM_001173977.1 Transcript intron_variant - - - - - - rs4577791 6:25387369 A CCDS54973.1 CCDS54973.1 Transcript intron_variant - - - - - - rs4577791 6:25387369 A ENSESTG00000029273 ENSESTT00000073742 Transcript intron_variant - - - - - - rs4577791 6:25387369 A ENSESTG00000029273 ENSESTT00000073764 Transcript intron_variant - - - - - - rs212933 6:25537296 G ENSESTG00000029359 ENSESTT00000074044 Transcript intron_variant - - - - - - rs212933 6:25537296 G 55604 NM_017640.5 Transcript intron_variant - - - - - - rs212933 6:25537296 G 55604 NM_001173977.1 Transcript intron_variant - - - - - - rs212933 6:25537296 G CCDS54973.1 CCDS54973.1 Transcript intron_variant - - - - - - rs1937128 6:25772476 A ENSESTG00000029549 ENSESTT00000074430 Transcript upstream_gene_variant - - - - - - DISTANCE=1371 rs1937128 6:25772476 A ENSESTG00000029549 ENSESTT00000074370 Transcript downstream_gene_variant - - - - - - DISTANCE=1997 rs1937128 6:25772476 A 10050 NM_005495.2 Transcript intron_variant - - - - - - rs1937128 6:25772476 A ENSESTG00000029549 ENSESTT00000074383 Transcript intron_variant - - - - - - rs1937128 6:25772476 A ENSESTG00000029549 ENSESTT00000074338 Transcript downstream_gene_variant - - - - - - DISTANCE=3057 rs1937128 6:25772476 A CCDS4564.1 CCDS4564.1 Transcript intron_variant - - - - - - rs1937128 6:25772476 A ENSESTG00000029549 ENSESTT00000074400 Transcript upstream_gene_variant - - - - - - DISTANCE=1177 rs199732 6:25901946 G - - - intergenic_variant - - - - - - rs2575171 6:25948539 C ENSESTG00000031151 ENSESTT00000078449 Transcript intron_variant - - - - - - rs169222 6:25986921 C CCDS4568.1 CCDS4568.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3006 rs169222 6:25986921 C ENSESTG00000031183 ENSESTT00000078629 Transcript downstream_gene_variant - - - - - - DISTANCE=2389 rs169222 6:25986921 C ENSESTG00000031183 ENSESTT00000078610 Transcript downstream_gene_variant - - - - - - DISTANCE=2389 rs169222 6:25986921 C 10475 NM_006355.3 Transcript 3_prime_UTR_variant 4993 - - - - - rs169222 6:25986921 C ENSESTG00000031151 ENSESTT00000078449 Transcript intron_variant - - - - - - rs198798 6:26140695 G ENSESTG00000031151 ENSESTT00000078449 Transcript downstream_gene_variant - - - - - - DISTANCE=2295 rs9358922 6:26311568 A - ENSR00001494249 RegulatoryFeature regulatory_region_variant - - - - - - rs9358922 6:26311568 A 100189430 NC_000006.11:TRNAS27:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1256 rs9358922 6:26311568 A 100189185 NC_000006.11:TRNAQ15:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=407 rs9358922 6:26311568 A 100189094 NC_000006.11:TRNAM6:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1784 rs9358922 6:26311568 A 100189321 NC_000006.11:TRNAQ25:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=73 rs1033402 6:26403290 A CCDS47388.1 CCDS47388.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2502 rs1033402 6:26403290 A CCDS47389.1 CCDS47389.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2502 rs1033402 6:26403290 A ENSESTG00000031025 ENSESTT00000078219 Transcript intron_variant - - - - - - rs1033402 6:26403290 A CCDS4608.1 CCDS4608.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2502 rs1033402 6:26403290 A CCDS4609.1 CCDS4609.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2502 rs1033402 6:26403290 A 11119 NM_007048.5 Transcript intron_variant - - - - - - rs1033402 6:26403290 A ENSESTG00000031025 ENSESTT00000078173 Transcript intron_variant - - - - - - rs1033402 6:26403290 A ENSESTG00000031025 ENSESTT00000078094 Transcript intron_variant - - - - - - rs1033402 6:26403290 A 11119 NM_001145008.1 Transcript intron_variant - - - - - - rs1033402 6:26403290 A 11119 NM_194441.2 Transcript intron_variant - - - - - - rs1033402 6:26403290 A ENSESTG00000031025 ENSESTT00000078085 Transcript intron_variant - - - - - - rs1033402 6:26403290 A 11119 NM_001145009.1 Transcript intron_variant - - - - - - rs1033402 6:26403290 A ENSESTG00000031025 ENSESTT00000078145 Transcript intron_variant - - - - - - rs1033402 6:26403290 A ENSESTG00000031025 ENSESTT00000078211 Transcript intron_variant - - - - - - rs6456807 6:28086076 G ENSESTG00000008086 ENSESTT00000020450 Transcript downstream_gene_variant - - - - - - DISTANCE=4557 rs6456807 6:28086076 G ENSESTG00000008086 ENSESTT00000020454 Transcript downstream_gene_variant - - - - - - DISTANCE=4223 rs6456807 6:28086076 G ENSESTG00000008086 ENSESTT00000020443 Transcript intron_variant - - - - - - rs478616 6:28088380 C 80345 NM_025231.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4007 rs478616 6:28088380 C ENSESTG00000007938 ENSESTT00000020062 Transcript upstream_gene_variant - - - - - - DISTANCE=3978 rs478616 6:28088380 C ENSESTG00000008086 ENSESTT00000020450 Transcript downstream_gene_variant - - - - - - DISTANCE=2253 rs478616 6:28088380 C CCDS4644.1 CCDS4644.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4842 rs478616 6:28088380 C ENSESTG00000008086 ENSESTT00000020454 Transcript downstream_gene_variant - - - - - - DISTANCE=1919 rs478616 6:28088380 C ENSESTG00000008086 ENSESTT00000020443 Transcript intron_variant - - - - - - rs4376347 6:28340872 A 80317 NM_001242894.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3918 rs4376347 6:28340872 A 80317 NM_024493.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3918 rs4376347 6:28340872 A 80317 NM_001242895.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3918 rs56322332 6:28687542 C - ENSR00001188801 RegulatoryFeature regulatory_region_variant - - - - - - rs56322332 6:28687542 C 100189092 NC_000006.11:TRNAA12:u_t_1 Transcript non_coding_exon_variant,nc_transcript_variant 62 - - - - - rs3132448 6:31634758 A 58496 NM_021221.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3970 rs3132448 6:31634758 A ENSESTG00000033213 ENSESTT00000083892 Transcript downstream_gene_variant - - - - - - DISTANCE=3655 rs3132448 6:31634758 A 7918 NM_001199237.1 Transcript upstream_gene_variant - - - - - - DISTANCE=698 rs3132448 6:31634758 A ENSESTG00000032469 ENSESTT00000081975 Transcript upstream_gene_variant - - - - - - DISTANCE=4050 rs3132448 6:31634758 A ENSESTG00000033216 ENSESTT00000083918 Transcript upstream_gene_variant - - - - - - DISTANCE=1151 rs3132448 6:31634758 A 7918 NM_001199239.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1119 rs3132448 6:31634758 A ENSESTG00000032469 ENSESTT00000081961 Transcript upstream_gene_variant - - - - - - DISTANCE=2137 rs3132448 6:31634758 A 1460 NM_001320.5 Transcript intron_variant - - - - - - rs3132448 6:31634758 A 7918 NM_033177.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1579 rs3132448 6:31634758 A CCDS34400.1 CCDS34400.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3970 rs3132448 6:31634758 A ENSESTG00000033216 ENSESTT00000083931 Transcript upstream_gene_variant - - - - - - DISTANCE=1184 rs3132448 6:31634758 A ENSESTG00000032429 ENSESTT00000081904 Transcript intron_variant - - - - - - rs3132448 6:31634758 A ENSESTG00000032478 ENSESTT00000081993 Transcript upstream_gene_variant - - - - - - DISTANCE=2430 rs3132448 6:31634758 A 7918 NM_001199240.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1351 rs3132448 6:31634758 A 7918 NM_001199238.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1119 rs3132448 6:31634758 A ENSESTG00000032429 ENSESTT00000081936 Transcript synonymous_variant 279 150 50 L ctG/ctA - rs3132448 6:31634758 A CCDS4712.1 CCDS4712.1 Transcript intron_variant - - - - - - rs3132448 6:31634758 A ENSESTG00000033234 ENSESTT00000083938 Transcript upstream_gene_variant - - - - - - DISTANCE=2887 rs3132448 6:31634758 A CCDS4711.1 CCDS4711.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2503 rs9267666 6:31870998 T CCDS4727.1 CCDS4727.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1916 rs9267666 6:31870998 T ENSESTG00000014145 ENSESTT00000035486 Transcript intron_variant - - - - - - rs9267666 6:31870998 T 717 NM_001178063.1 Transcript intron_variant - - - - - - rs9267666 6:31870998 T 221527 NM_181842.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1229 rs9267666 6:31870998 T ENSESTG00000014145 ENSESTT00000035484 Transcript intron_variant - - - - - - rs9267666 6:31870998 T CCDS56416.1 CCDS56416.1 Transcript intron_variant - - - - - - rs9267666 6:31870998 T ENSESTG00000014145 ENSESTT00000035501 Transcript intron_variant - - - - - - rs9267666 6:31870998 T ENSESTG00000014145 ENSESTT00000035503 Transcript intron_variant - - - - - - rs9267666 6:31870998 T ENSESTG00000014145 ENSESTT00000035495 Transcript intron_variant - - - - - - rs3129201 6:33147589 G 1302 NM_080680.2 Transcript splice_region_variant,intron_variant - - - - - - rs3129201 6:33147589 G CCDS43452.1 CCDS43452.1 Transcript splice_region_variant,intron_variant - - - - - - rs3129201 6:33147589 G 1302 NM_080681.2 Transcript splice_region_variant,intron_variant - - - - - - rs3129201 6:33147589 G 1302 NM_080679.2 Transcript splice_region_variant,intron_variant - - - - - - rs3106193 6:33374913 C CCDS34430.1 CCDS34430.1 Transcript intron_variant - - - - - - rs3106193 6:33374913 C ENSESTG00000016969 ENSESTT00000042695 Transcript upstream_gene_variant - - - - - - DISTANCE=3263 rs3106193 6:33374913 C 5252 NR_027692.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3860 rs3106193 6:33374913 C ENSESTG00000016969 ENSESTT00000042747 Transcript upstream_gene_variant - - - - - - DISTANCE=3862 rs3106193 6:33374913 C ENSESTG00000016969 ENSESTT00000042721 Transcript upstream_gene_variant - - - - - - DISTANCE=3263 rs3106193 6:33374913 C ENSESTG00000016920 ENSESTT00000042457 Transcript intron_variant - - - - - - rs3106193 6:33374913 C 5252 NM_002636.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3860 rs3106193 6:33374913 C ENSESTG00000016920 ENSESTT00000042537 Transcript intron_variant - - - - - - rs3106193 6:33374913 C ENSESTG00000016920 ENSESTT00000042528 Transcript 3_prime_UTR_variant 2214 - - - - - rs3106193 6:33374913 C 3833 NM_002263.3 Transcript intron_variant - - - - - - rs3106193 6:33374913 C ENSESTG00000016969 ENSESTT00000042744 Transcript upstream_gene_variant - - - - - - DISTANCE=3862 rs3106193 6:33374913 C 5252 NM_024165.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3860 rs2495959 6:33917641 G - - - intergenic_variant - - - - - - rs2499770 6:33963609 G 100302123 NR_031681.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4140 rs913013 6:34505121 G CCDS4794.1 CCDS4794.1 Transcript downstream_gene_variant - - - - - - DISTANCE=930 rs913013 6:34505121 G CCDS59013.1 CCDS59013.1 Transcript downstream_gene_variant - - - - - - DISTANCE=930 rs913013 6:34505121 G ENSESTG00000033839 ENSESTT00000085597 Transcript downstream_gene_variant - - - - - - DISTANCE=4680 rs913013 6:34505121 G 29993 NM_001199583.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1082 rs913013 6:34505121 G 29993 NM_020804.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1082 rs913013 6:34505121 G CCDS4793.1 CCDS4793.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4814 rs913013 6:34505121 G 25803 NM_012391.2 Transcript downstream_gene_variant - - - - - - DISTANCE=458 rs913013 6:34505121 G ENSESTG00000033839 ENSESTT00000085606 Transcript downstream_gene_variant - - - - - - DISTANCE=2117 rs913013 6:34505121 G 25803 NM_001252294.1 Transcript downstream_gene_variant - - - - - - DISTANCE=458 rs2744945 6:34641500 A - ENSR00001214980 RegulatoryFeature regulatory_region_variant - - - - - - rs2744945 6:34641500 A ENSESTG00000033921 ENSESTT00000085727 Transcript intron_variant - - - - - - rs2744945 6:34641500 A CCDS4795.1 CCDS4795.1 Transcript intron_variant - - - - - - rs2744945 6:34641500 A ENSESTG00000033921 ENSESTT00000085723 Transcript intron_variant - - - - - - rs2744945 6:34641500 A CCDS4796.1 CCDS4796.1 Transcript intron_variant - - - - - - rs2744945 6:34641500 A 64771 NM_022758.4 Transcript intron_variant - - - - - - rs2744945 6:34641500 A ENSESTG00000033921 ENSESTT00000085741 Transcript intron_variant - - - - - - rs2744945 6:34641500 A 64771 NM_024294.2 Transcript intron_variant - - - - - - rs2140417 6:34980367 C 23294 NM_015245.2 Transcript intron_variant - - - - - - rs2140417 6:34980367 C ENSESTG00000023657 ENSESTT00000059800 Transcript upstream_gene_variant - - - - - - DISTANCE=4440 rs2140417 6:34980367 C ENSESTG00000023657 ENSESTT00000059750 Transcript upstream_gene_variant - - - - - - DISTANCE=4440 rs2140417 6:34980367 C ENSESTG00000023657 ENSESTT00000059654 Transcript intron_variant - - - - - - rs2140417 6:34980367 C ENSESTG00000023657 ENSESTT00000059811 Transcript upstream_gene_variant - - - - - - DISTANCE=4915 rs2140417 6:34980367 C CCDS4798.1 CCDS4798.1 Transcript intron_variant - - - - - - rs1996914 6:35000298 T - ENSR00001215066 RegulatoryFeature regulatory_region_variant - - - - - - rs1996914 6:35000298 T 23294 NM_015245.2 Transcript intron_variant - - - - - - rs1996914 6:35000298 T ENSESTG00000023657 ENSESTT00000059800 Transcript intron_variant - - - - - - rs1996914 6:35000298 T ENSESTG00000023657 ENSESTT00000059750 Transcript intron_variant - - - - - - rs1996914 6:35000298 T ENSESTG00000023657 ENSESTT00000059898 Transcript intron_variant - - - - - - rs1996914 6:35000298 T ENSESTG00000023657 ENSESTT00000059654 Transcript intron_variant - - - - - - rs1996914 6:35000298 T CCDS4798.1 CCDS4798.1 Transcript intron_variant - - - - - - rs1996914 6:35000298 T ENSESTG00000023657 ENSESTT00000059918 Transcript intron_variant - - - - - - rs1996914 6:35000298 T ENSESTG00000023657 ENSESTT00000059811 Transcript intron_variant - - - - - - rs9348973 6:35355426 G CCDS54994.1 CCDS54994.1 Transcript intron_variant - - - - - - rs9348973 6:35355426 G 5467 NM_001171820.1 Transcript intron_variant - - - - - - rs9348973 6:35355426 G ENSESTG00000024248 ENSESTT00000061441 Transcript intron_variant - - - - - - rs9348973 6:35355426 G ENSESTG00000024248 ENSESTT00000061307 Transcript intron_variant - - - - - - rs9348973 6:35355426 G ENSESTG00000024248 ENSESTT00000061405 Transcript intron_variant - - - - - - rs9348973 6:35355426 G ENSESTG00000024248 ENSESTT00000061395 Transcript intron_variant - - - - - - rs9348973 6:35355426 G 5467 NM_006238.4 Transcript intron_variant - - - - - - rs9348973 6:35355426 G 5467 NM_177435.2 Transcript intron_variant - - - - - - rs9348973 6:35355426 G 5467 NM_001171818.1 Transcript intron_variant - - - - - - rs9348973 6:35355426 G 5467 NM_001171819.1 Transcript intron_variant - - - - - - rs9348973 6:35355426 G ENSESTG00000024248 ENSESTT00000061467 Transcript intron_variant - - - - - - rs9348973 6:35355426 G ENSESTG00000024248 ENSESTT00000061505 Transcript intron_variant - - - - - - rs9348973 6:35355426 G ENSESTG00000024248 ENSESTT00000061490 Transcript intron_variant - - - - - - rs9348973 6:35355426 G ENSESTG00000024248 ENSESTT00000061518 Transcript intron_variant - - - - - - rs2817034 6:35696289 C - ENSR00001215285 RegulatoryFeature regulatory_region_variant - - - - - - rs2817034 6:35696289 C 285847 NR_027117.1 Transcript non_coding_exon_variant,nc_transcript_variant 1300 - - - - - rs2817034 6:35696289 C 2289 NM_001145775.1 Transcript 5_prime_UTR_variant 72 - - - - - rs662384 6:36454200 G ENSESTG00000028801 ENSESTT00000072477 Transcript upstream_gene_variant - - - - - - DISTANCE=1142 rs662384 6:36454200 G CCDS4821.1 CCDS4821.1 Transcript intron_variant - - - - - - rs662384 6:36454200 G ENSESTG00000028748 ENSESTT00000072460 Transcript intron_variant - - - - - - rs662384 6:36454200 G ENSESTG00000028748 ENSESTT00000072436 Transcript intron_variant - - - - - - rs662384 6:36454200 G 222658 NM_173562.3 Transcript intron_variant - - - - - - rs568220 6:36555004 T - - - intergenic_variant - - - - - - rs1034062 6:37022725 C - - - intergenic_variant - - - - - - rs1224387 6:37069342 T - ENSR00001494949 RegulatoryFeature regulatory_region_variant - - - - - - rs1224387 6:37069342 T - - - intergenic_variant - - - - - - rs9296214 6:37079166 A - - - intergenic_variant - - - - - - rs6457982 6:37096504 A - ENSR00001215728 RegulatoryFeature regulatory_region_variant - - - - - - rs6457982 6:37096504 A - - - intergenic_variant - - - - - - rs371160 6:37236740 T 55633 NM_017772.2 Transcript intron_variant - - - - - - rs371160 6:37236740 T ENSESTG00000008773 ENSESTT00000022090 Transcript intron_variant - - - - - - rs371160 6:37236740 T CCDS4832.1 CCDS4832.1 Transcript intron_variant - - - - - - rs6911956 6:38492121 T CCDS54998.1 CCDS54998.1 Transcript intron_variant - - - - - - rs6911956 6:38492121 T CCDS47418.1 CCDS47418.1 Transcript intron_variant - - - - - - rs6911956 6:38492121 T 114781 NM_001099272.1 Transcript intron_variant - - - - - - rs6911956 6:38492121 T CCDS43458.1 CCDS43458.1 Transcript intron_variant - - - - - - rs6911956 6:38492121 T 114781 NM_152733.2 Transcript intron_variant - - - - - - rs6911956 6:38492121 T 114781 NM_052893.1 Transcript intron_variant - - - - - - rs6911956 6:38492121 T 114781 NM_001172418.1 Transcript intron_variant - - - - - - rs1678705 6:38787020 A 1769 NM_001206927.1 Transcript intron_variant - - - - - - rs9380819 6:38964202 C 1769 NM_001206927.1 Transcript intron_variant - - - - - - rs9380819 6:38964202 C ENSESTG00000012402 ENSESTT00000031092 Transcript intron_variant - - - - - - rs1923468 6:39964026 T - - - intergenic_variant - - - - - - rs847782 6:40053779 C - - - intergenic_variant - - - - - - rs1464719 6:40116760 A - ENSR00001216337 RegulatoryFeature regulatory_region_variant - - - - - - rs1464719 6:40116760 A - - - intergenic_variant - - - - - - rs2504841 6:40426386 C ENSESTG00000018281 ENSESTT00000046064 Transcript intron_variant - - - - - - rs2504841 6:40426386 C 57497 NM_020737.1 Transcript intron_variant - - - - - - rs6932770 6:40656849 G - - - intergenic_variant - - - - - - rs6458176 6:40694336 G - - - intergenic_variant - - - - - - rs4714373 6:40712855 C - - - intergenic_variant - - - - - - rs4714377 6:40732768 G - - - intergenic_variant - - - - - - rs2803511 6:41241072 G 54210 NM_001242590.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1927 rs2803511 6:41241072 G CCDS4854.1 CCDS4854.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2791 rs2803511 6:41241072 G ENSESTG00000012306 ENSESTT00000030871 Transcript downstream_gene_variant - - - - - - DISTANCE=2666 rs2803511 6:41241072 G CCDS56427.1 CCDS56427.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2850 rs2803511 6:41241072 G 54210 NM_018643.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1927 rs4301293 6:42090302 C - ENSR00001216731 RegulatoryFeature regulatory_region_variant - - - - - - rs4301293 6:42090302 C CCDS47428.1 CCDS47428.1 Transcript intron_variant - - - - - - rs4301293 6:42090302 C ENSESTG00000018403 ENSESTT00000046324 Transcript intron_variant - - - - - - rs4301293 6:42090302 C 647024 NM_001164446.1 Transcript intron_variant - - - - - - rs6911399 6:42110263 C - ENSR00001216741 RegulatoryFeature regulatory_region_variant - - - - - - rs6911399 6:42110263 C CCDS47428.1 CCDS47428.1 Transcript upstream_gene_variant - - - - - - DISTANCE=81 rs6911399 6:42110263 C 647024 NM_001164446.1 Transcript 5_prime_UTR_variant 453 - - - - - rs6458279 6:42223760 T ENSESTG00000018286 ENSESTT00000046108 Transcript intron_variant - - - - - - rs6458279 6:42223760 T CCDS4867.1 CCDS4867.1 Transcript intron_variant - - - - - - rs6458279 6:42223760 T ENSESTG00000018286 ENSESTT00000046066 Transcript intron_variant - - - - - - rs6458279 6:42223760 T 55809 NM_033502.2 Transcript intron_variant - - - - - - rs660104 6:42302193 A ENSESTG00000018242 ENSESTT00000045989 Transcript intron_variant - - - - - - rs660104 6:42302193 A ENSESTG00000018242 ENSESTT00000045972 Transcript intron_variant - - - - - - rs660104 6:42302193 A ENSESTG00000018242 ENSESTT00000046034 Transcript intron_variant - - - - - - rs660104 6:42302193 A ENSESTG00000018242 ENSESTT00000046009 Transcript intron_variant - - - - - - rs660104 6:42302193 A ENSESTG00000018242 ENSESTT00000045957 Transcript intron_variant - - - - - - rs660104 6:42302193 A 55809 NM_033502.2 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045661 Transcript upstream_gene_variant - - - - - - DISTANCE=466 rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045613 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045541 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045409 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045325 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045560 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045461 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045441 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045648 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045486 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045639 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045626 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045576 Transcript intron_variant - - - - - - rs1016248 6:42617350 T CCDS4870.1 CCDS4870.1 Transcript intron_variant - - - - - - rs1016248 6:42617350 T 23304 NM_015255.2 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045517 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045591 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045423 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045631 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045477 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045498 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045550 Transcript intron_variant - - - - - - rs1016248 6:42617350 T ENSESTG00000017881 ENSESTT00000045490 Transcript intron_variant - - - - - - rs222222 6:42680049 C ENSESTG00000018228 ENSESTT00000045920 Transcript intron_variant - - - - - - rs222222 6:42680049 C CCDS4871.1 CCDS4871.1 Transcript intron_variant - - - - - - rs222222 6:42680049 C 5961 NM_000322.4 Transcript intron_variant - - - - - - rs1889530 6:43048890 C - ENSR00001216982 RegulatoryFeature regulatory_region_variant - - - - - - rs1889530 6:43048890 C CCDS4884.1 CCDS4884.1 Transcript intron_variant - - - - - - rs1889530 6:43048890 C CCDS59021.1 CCDS59021.1 Transcript intron_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007025 Transcript intron_variant - - - - - - rs1889530 6:43048890 C CCDS4885.1 CCDS4885.1 Transcript intron_variant - - - - - - rs1889530 6:43048890 C CCDS4887.1 CCDS4887.1 Transcript intron_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007057 Transcript intron_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007063 Transcript intron_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007059 Transcript intron_variant - - - - - - rs1889530 6:43048890 C 5754 NR_072998.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007044 Transcript intron_variant - - - - - - rs1889530 6:43048890 C CCDS4886.1 CCDS4886.1 Transcript intron_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007060 Transcript intron_variant - - - - - - rs1889530 6:43048890 C 5754 NM_152882.3 Transcript intron_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007039 Transcript intron_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007062 Transcript intron_variant - - - - - - rs1889530 6:43048890 C 5754 NM_152880.3 Transcript intron_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007038 Transcript intron_variant - - - - - - rs1889530 6:43048890 C ENSESTG00000002817 ENSESTT00000007029 Transcript intron_variant - - - - - - rs1889530 6:43048890 C 5754 NM_152881.3 Transcript intron_variant - - - - - - rs1889530 6:43048890 C 5754 NR_072997.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1889530 6:43048890 C 5754 NM_001270398.1 Transcript intron_variant - - - - - - rs1889530 6:43048890 C 5754 NM_002821.4 Transcript intron_variant - - - - - - rs941849 6:43154091 G ENSESTG00000002870 ENSESTT00000007144 Transcript downstream_gene_variant - - - - - - DISTANCE=357 rs941849 6:43154091 G ENSESTG00000002878 ENSESTT00000007148 Transcript synonymous_variant 313 240 80 L ctC/ctG - rs941849 6:43154091 G ENSESTG00000003305 ENSESTT00000008229 Transcript upstream_gene_variant - - - - - - DISTANCE=4892 rs941849 6:43154091 G ENSESTG00000002859 ENSESTT00000007127 Transcript downstream_gene_variant - - - - - - DISTANCE=4852 rs941849 6:43154091 G ENSESTG00000002878 ENSESTT00000007167 Transcript upstream_gene_variant - - - - - - DISTANCE=1651 rs941849 6:43154091 G ENSESTG00000002870 ENSESTT00000007145 Transcript downstream_gene_variant - - - - - - DISTANCE=800 rs941849 6:43154091 G 6722 NM_003131.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4847 rs941849 6:43154091 G ENSESTG00000002878 ENSESTT00000007155 Transcript upstream_gene_variant - - - - - - DISTANCE=575 rs941849 6:43154091 G 23113 NM_015089.2 Transcript synonymous_variant 1224 1149 383 L ctC/ctG - rs941849 6:43154091 G CCDS4890.1 CCDS4890.1 Transcript synonymous_variant 1149 1149 383 L ctC/ctG - rs941849 6:43154091 G ENSESTG00000002859 ENSESTT00000007118 Transcript downstream_gene_variant - - - - - - DISTANCE=4852 rs1150799 6:43453969 C ENSESTG00000003026 ENSESTT00000007567 Transcript intron_variant - - - - - - rs1150799 6:43453969 C ENSESTG00000003026 ENSESTT00000007570 Transcript intron_variant - - - - - - rs1150799 6:43453969 C 93643 NM_001146016.1 Transcript intron_variant - - - - - - rs1150799 6:43453969 C ENSESTG00000003026 ENSESTT00000007587 Transcript upstream_gene_variant - - - - - - DISTANCE=3353 rs1150799 6:43453969 C 93643 NM_001146017.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3353 rs1150799 6:43453969 C 93643 NM_080604.2 Transcript intron_variant - - - - - - rs1150799 6:43453969 C 93643 NM_001146018.1 Transcript intron_variant - - - - - - rs1150799 6:43453969 C 93643 NM_001146020.1 Transcript intron_variant - - - - - - rs1150799 6:43453969 C ENSESTG00000003026 ENSESTT00000007565 Transcript intron_variant - - - - - - rs1150799 6:43453969 C 93643 NR_027394.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1150799 6:43453969 C 93643 NM_001146019.1 Transcript intron_variant - - - - - - rs1150800 6:43494319 G ENSESTG00000003214 ENSESTT00000008034 Transcript intron_variant - - - - - - rs1150800 6:43494319 G CCDS47430.1 CCDS47430.1 Transcript intron_variant - - - - - - rs1150800 6:43494319 G ENSESTG00000003214 ENSESTT00000008041 Transcript intron_variant - - - - - - rs1150800 6:43494319 G 57510 NM_020750.2 Transcript intron_variant - - - - - - rs499853 6:44796180 C 8464 NM_001261823.1 Transcript 3_prime_UTR_variant 2520 - - - - - rs499853 6:44796180 C ENSESTG00000024006 ENSESTT00000060673 Transcript downstream_gene_variant - - - - - - DISTANCE=1276 rs499853 6:44796180 C ENSESTG00000024006 ENSESTT00000060649 Transcript intron_variant - - - - - - rs499853 6:44796180 C CCDS34466.1 CCDS34466.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1373 rs499853 6:44796180 C 8464 NM_181356.2 Transcript 3_prime_UTR_variant 2796 - - - - - rs499853 6:44796180 C 8464 NM_003599.3 Transcript 3_prime_UTR_variant 2611 - - - - - rs499853 6:44796180 C CCDS34465.1 CCDS34465.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1373 rs499853 6:44796180 C ENSESTG00000033116 ENSESTT00000083670 Transcript intron_variant - - - - - - rs1324539 6:45212400 T 8464 NM_001261823.1 Transcript intron_variant - - - - - - rs1324539 6:45212400 T 8464 NM_003599.3 Transcript intron_variant - - - - - - rs1324539 6:45212400 T 8464 NM_181356.2 Transcript intron_variant - - - - - - rs1324539 6:45212400 T CCDS34465.1 CCDS34465.1 Transcript intron_variant - - - - - - rs1324539 6:45212400 T ENSESTG00000023994 ENSESTT00000060547 Transcript intron_variant - - - - - - rs1324539 6:45212400 T CCDS34466.1 CCDS34466.1 Transcript intron_variant - - - - - - rs9381379 6:45213293 G 8464 NM_001261823.1 Transcript intron_variant - - - - - - rs9381379 6:45213293 G 8464 NM_003599.3 Transcript intron_variant - - - - - - rs9381379 6:45213293 G 8464 NM_181356.2 Transcript intron_variant - - - - - - rs9381379 6:45213293 G CCDS34465.1 CCDS34465.1 Transcript intron_variant - - - - - - rs9381379 6:45213293 G ENSESTG00000023994 ENSESTT00000060547 Transcript intron_variant - - - - - - rs9381379 6:45213293 G CCDS34466.1 CCDS34466.1 Transcript intron_variant - - - - - - rs2144474 6:45377944 A CCDS43468.2 CCDS43468.2 Transcript intron_variant - - - - - - rs2144474 6:45377944 A CCDS43467.2 CCDS43467.2 Transcript intron_variant - - - - - - rs2144474 6:45377944 A 860 NM_001024630.3 Transcript intron_variant - - - - - - rs2144474 6:45377944 A 860 NM_001015051.3 Transcript intron_variant - - - - - - rs9472544 6:45634910 C - ENSR00001217672 RegulatoryFeature regulatory_region_variant - - - - - - rs9472544 6:45634910 C ENSESTG00000023988 ENSESTT00000060522 Transcript downstream_gene_variant - - - - - - DISTANCE=1626 rs9357494 6:45811931 G - ENSR00001217699 RegulatoryFeature regulatory_region_variant - - - - - - rs9357494 6:45811931 G - - - intergenic_variant - - - - - - rs1554788 6:46440577 A 10231 NM_001251973.1 Transcript intron_variant - - - - - - rs1554788 6:46440577 A 10231 NM_001251974.1 Transcript intron_variant - - - - - - rs9367254 6:46707420 C 7941 NM_005084.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4269 rs9367254 6:46707420 C 7941 NM_001168357.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3990 rs2039502 6:47487069 T - ENSR00001495804 RegulatoryFeature regulatory_region_variant - - - - - - rs2039502 6:47487069 T 23607 NM_012120.2 Transcript intron_variant - - - - - - rs2039502 6:47487069 T ENSESTG00000033948 ENSESTT00000085831 Transcript intron_variant - - - - - - rs2039502 6:47487069 T CCDS34472.1 CCDS34472.1 Transcript intron_variant - - - - - - rs1887898 6:47845646 G 442213 NM_001013732.3 Transcript downstream_gene_variant - - - - - - DISTANCE=118 rs1887898 6:47845646 G ENSESTG00000028840 ENSESTT00000072567 Transcript downstream_gene_variant - - - - - - DISTANCE=1904 rs1887898 6:47845646 G CCDS34473.2 CCDS34473.2 Transcript downstream_gene_variant - - - - - - DISTANCE=393 rs1570076 6:47972015 T 442213 NM_001013732.3 Transcript intron_variant - - - - - - rs1570076 6:47972015 T ENSESTG00000028840 ENSESTT00000072567 Transcript intron_variant - - - - - - rs1570076 6:47972015 T ENSESTG00000028840 ENSESTT00000072557 Transcript downstream_gene_variant - - - - - - DISTANCE=4540 rs1570076 6:47972015 T CCDS34473.2 CCDS34473.2 Transcript intron_variant - - - - - - rs1570076 6:47972015 T 442213 NM_207499.2 Transcript intron_variant - - - - - - rs1150814 6:48172645 A - - - intergenic_variant - - - - - - rs2396877 6:48606128 A - - - intergenic_variant - - - - - - rs2253100 6:48684038 T - - - intergenic_variant - - - - - - rs2477404 6:49375322 A - - - intergenic_variant - - - - - - rs360551 6:49747942 G - - - intergenic_variant - - - - - - rs2786834 6:49837490 A 167 NM_001131.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3272 rs2786834 6:49837490 A 167 NM_170609.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3272 rs2786834 6:49837490 A ENSESTG00000008710 ENSESTT00000021870 Transcript intron_variant - - - - - - rs2786834 6:49837490 A 167 NM_001205220.1 Transcript intron_variant - - - - - - rs601501 6:50044906 G - - - intergenic_variant - - - - - - rs586485 6:50055166 C - ENSR00001495906 RegulatoryFeature regulatory_region_variant - - - - - - rs586485 6:50055166 C - - - intergenic_variant - - - - - - rs1771283 6:50218709 C - - - intergenic_variant - - - - - - rs6933403 6:50377140 C - - - intergenic_variant - - - - - - rs7746101 6:51969551 C - - - intergenic_variant - - - - - - rs1413924 6:52046047 G - - - intergenic_variant - - - - - - rs316143 6:52881488 T CCDS4949.1 CCDS4949.1 Transcript intron_variant - - - - - - rs316143 6:52881488 T 22858 NM_014920.3 Transcript intron_variant - - - - - - rs316143 6:52881488 T 22858 NM_016513.4 Transcript intron_variant - - - - - - rs222447 6:52917726 G 22858 NM_014920.3 Transcript intron_variant - - - - - - rs222447 6:52917726 G 22858 NM_016513.4 Transcript intron_variant - - - - - - rs6919768 6:52985368 G ENSESTG00000007991 ENSESTT00000020172 Transcript intron_variant - - - - - - rs1536385 6:53503497 G - - - intergenic_variant - - - - - - rs1325827 6:53942832 A ENSESTG00000034503 ENSESTT00000087279 Transcript intron_variant - - - - - - rs1325827 6:53942832 A CCDS4954.1 CCDS4954.1 Transcript intron_variant - - - - - - rs1325827 6:53942832 A 90523 NM_138569.2 Transcript intron_variant - - - - - - rs547413 6:53954166 C ENSESTG00000034503 ENSESTT00000087279 Transcript intron_variant - - - - - - rs547413 6:53954166 C CCDS4954.1 CCDS4954.1 Transcript intron_variant - - - - - - rs547413 6:53954166 C 90523 NM_138569.2 Transcript intron_variant - - - - - - rs535118 6:53974363 C ENSESTG00000034503 ENSESTT00000087279 Transcript intron_variant - - - - - - rs535118 6:53974363 C ENSESTG00000034503 ENSESTT00000087291 Transcript upstream_gene_variant - - - - - - DISTANCE=1882 rs535118 6:53974363 C ENSESTG00000034503 ENSESTT00000087285 Transcript intron_variant - - - - - - rs535118 6:53974363 C CCDS4954.1 CCDS4954.1 Transcript intron_variant - - - - - - rs535118 6:53974363 C 90523 NM_138569.2 Transcript intron_variant - - - - - - rs535118 6:53974363 C ENSESTG00000034503 ENSESTT00000087293 Transcript upstream_gene_variant - - - - - - DISTANCE=1914 rs535118 6:53974363 C ENSESTG00000034503 ENSESTT00000087289 Transcript intron_variant - - - - - - rs1775797 6:54069519 A ENSESTG00000034519 ENSESTT00000087304 Transcript intron_variant - - - - - - rs1775797 6:54069519 A CCDS4954.1 CCDS4954.1 Transcript intron_variant - - - - - - rs1775797 6:54069519 A 90523 NM_138569.2 Transcript intron_variant - - - - - - rs1775797 6:54069519 A ENSESTG00000034519 ENSESTT00000087309 Transcript intron_variant - - - - - - rs2754787 6:54090400 C ENSESTG00000034519 ENSESTT00000087304 Transcript intron_variant - - - - - - rs2754787 6:54090400 C CCDS4954.1 CCDS4954.1 Transcript intron_variant - - - - - - rs2754787 6:54090400 C 90523 NM_138569.2 Transcript intron_variant - - - - - - rs2754787 6:54090400 C ENSESTG00000034519 ENSESTT00000087309 Transcript intron_variant - - - - - - rs6458991 6:54161626 A - - - intergenic_variant - - - - - - rs606444 6:54176518 T ENSESTG00000034529 ENSESTT00000087345 Transcript intron_variant - - - - - - rs606444 6:54176518 T 27283 NM_014464.3 Transcript intron_variant - - - - - - rs606444 6:54176518 T ENSESTG00000034529 ENSESTT00000087348 Transcript intron_variant - - - - - - rs606444 6:54176518 T ENSESTG00000034529 ENSESTT00000087336 Transcript intron_variant - - - - - - rs606444 6:54176518 T ENSESTG00000034529 ENSESTT00000087332 Transcript intron_variant - - - - - - rs606444 6:54176518 T CCDS4955.1 CCDS4955.1 Transcript intron_variant - - - - - - rs606444 6:54176518 T ENSESTG00000034529 ENSESTT00000087339 Transcript intron_variant - - - - - - rs606444 6:54176518 T ENSESTG00000034529 ENSESTT00000087347 Transcript intron_variant - - - - - - rs606444 6:54176518 T ENSESTG00000034529 ENSESTT00000087342 Transcript intron_variant - - - - - - rs674157 6:54203174 C ENSESTG00000034529 ENSESTT00000087345 Transcript intron_variant - - - - - - rs674157 6:54203174 C 27283 NM_014464.3 Transcript intron_variant - - - - - - rs674157 6:54203174 C CCDS4955.1 CCDS4955.1 Transcript intron_variant - - - - - - rs674157 6:54203174 C ENSESTG00000034529 ENSESTT00000087332 Transcript intron_variant - - - - - - rs243817 6:54297158 C - - - intergenic_variant - - - - - - rs1745080 6:54481227 G - - - intergenic_variant - - - - - - rs10807480 6:54672835 A - - - intergenic_variant - - - - - - rs171225 6:54777647 G ENSESTG00000000038 ENSESTT00000000114 Transcript intron_variant - - - - - - rs171225 6:54777647 G CCDS34479.1 CCDS34479.1 Transcript intron_variant - - - - - - rs171225 6:54777647 G 222584 NM_001010872.1 Transcript intron_variant - - - - - - rs171225 6:54777647 G ENSESTG00000034548 ENSESTT00000087366 Transcript intron_variant - - - - - - rs3125274 6:54863677 G - - - intergenic_variant - - - - - - rs3105256 6:54863758 T - - - intergenic_variant - - - - - - rs3105248 6:54865582 T - - - intergenic_variant - - - - - - rs4329118 6:54866856 T - - - intergenic_variant - - - - - - rs6459038 6:54867434 G - - - intergenic_variant - - - - - - rs6459039 6:54867494 C - - - intergenic_variant - - - - - - rs6459040 6:54867511 G - - - intergenic_variant - - - - - - rs3125277 6:54867692 C - - - intergenic_variant - - - - - - rs3125278 6:54868079 A - - - intergenic_variant - - - - - - rs3125279 6:54868738 G - - - intergenic_variant - - - - - - rs3125280 6:54869079 A - - - intergenic_variant - - - - - - rs4267957 6:54870976 G - - - intergenic_variant - - - - - - rs6914723 6:54875440 T - - - intergenic_variant - - - - - - rs6937812 6:54875546 G - - - intergenic_variant - - - - - - rs4715495 6:54876363 C - - - intergenic_variant - - - - - - rs6459051 6:54878860 G - - - intergenic_variant - - - - - - rs4236117 6:54879759 G - ENSR00001218955 RegulatoryFeature regulatory_region_variant - - - - - - rs4236117 6:54879759 G - - - intergenic_variant - - - - - - rs4715496 6:54885329 A - - - intergenic_variant - - - - - - rs9370369 6:54885563 C - - - intergenic_variant - - - - - - rs4386807 6:54887011 G - - - intergenic_variant - - - - - - rs4421183 6:54889102 C - - - intergenic_variant - - - - - - rs4489156 6:54889800 A - - - intergenic_variant - - - - - - rs9382429 6:54892977 G - - - intergenic_variant - - - - - - rs4327696 6:54894056 C - - - intergenic_variant - - - - - - rs4610567 6:54896185 G - - - intergenic_variant - - - - - - rs7740553 6:54901296 C - - - intergenic_variant - - - - - - rs4484523 6:54905067 C - ENSR00001496250 RegulatoryFeature regulatory_region_variant - - - - - - rs4484523 6:54905067 C - - - intergenic_variant - - - - - - rs4610569 6:54905968 C - - - intergenic_variant - - - - - - rs4628098 6:54906050 G - - - intergenic_variant - - - - - - rs4236118 6:54908766 A - - - intergenic_variant - - - - - - rs4605885 6:54912395 A - ENSR00001218960 RegulatoryFeature regulatory_region_variant - - - - - - rs4605885 6:54912395 A - - - intergenic_variant - - - - - - rs4613825 6:54916808 A - - - intergenic_variant - - - - - - rs7771892 6:54919249 T - - - intergenic_variant - - - - - - rs4410725 6:54919925 C - - - intergenic_variant - - - - - - rs4613809 6:54922203 A - - - intergenic_variant - - - - - - rs9396033 6:54922937 G - - - intergenic_variant - - - - - - rs4311498 6:54927819 G - - - intergenic_variant - - - - - - rs4415158 6:54929441 A - - - intergenic_variant - - - - - - rs4440460 6:54933376 G - - - intergenic_variant - - - - - - rs6900396 6:54933998 C - ENSR00001496253 RegulatoryFeature regulatory_region_variant - - - - - - rs6900396 6:54933998 C - - - intergenic_variant - - - - - - rs7745727 6:54935757 C - - - intergenic_variant - - - - - - rs9382443 6:54936114 A - - - intergenic_variant - - - - - - rs6939179 6:54937233 C - - - intergenic_variant - - - - - - rs4583975 6:54939157 C - - - intergenic_variant - - - - - - rs4351264 6:54945636 G - - - intergenic_variant - - - - - - rs9349750 6:54946259 T - - - intergenic_variant - - - - - - rs9367610 6:54946344 A - - - intergenic_variant - - - - - - rs4715510 6:54952049 T - - - intergenic_variant - - - - - - rs4236119 6:54952838 T - - - intergenic_variant - - - - - - rs6929789 6:54960866 T - - - intergenic_variant - - - - - - rs4317396 6:54968955 C - - - intergenic_variant - - - - - - rs9475141 6:54969930 G - - - intergenic_variant - - - - - - rs4236124 6:54971742 T - - - intergenic_variant - - - - - - rs9475143 6:54975002 A - - - intergenic_variant - - - - - - rs4308558 6:54981965 T - - - intergenic_variant - - - - - - rs4308559 6:54982116 T - - - intergenic_variant - - - - - - rs4236126 6:54996272 A - - - intergenic_variant - - - - - - rs9370385 6:54998074 G - - - intergenic_variant - - - - - - rs4566887 6:54999742 G - - - intergenic_variant - - - - - - rs9349759 6:55003132 C - - - intergenic_variant - - - - - - rs6941871 6:55004096 C - - - intergenic_variant - - - - - - rs7743951 6:55005640 C - - - intergenic_variant - - - - - - rs4712097 6:55006319 C - - - intergenic_variant - - - - - - rs4469294 6:55006887 A - - - intergenic_variant - - - - - - rs9396084 6:55217554 C 389400 NM_207410.2 Transcript intron_variant - - - - - - rs9396084 6:55217554 C CCDS4957.1 CCDS4957.1 Transcript intron_variant - - - - - - rs7755168 6:55247710 T 389400 NM_207410.2 Transcript intron_variant - - - - - - rs7755168 6:55247710 T CCDS4957.1 CCDS4957.1 Transcript intron_variant - - - - - - rs4715546 6:55289608 A - - - intergenic_variant - - - - - - rs9396100 6:55367394 T ENSESTG00000000053 ENSESTT00000000145 Transcript intron_variant - - - - - - rs9396100 6:55367394 T 54511 NM_001042406.1 Transcript intron_variant - - - - - - rs9396100 6:55367394 T ENSESTG00000000053 ENSESTT00000000146 Transcript intron_variant - - - - - - rs9396100 6:55367394 T CCDS43474.1 CCDS43474.1 Transcript intron_variant - - - - - - rs9396100 6:55367394 T ENSESTG00000000053 ENSESTT00000000141 Transcript intron_variant - - - - - - rs9396100 6:55367394 T 54511 NM_019036.2 Transcript intron_variant - - - - - - rs9396100 6:55367394 T ENSESTG00000000053 ENSESTT00000000139 Transcript intron_variant - - - - - - rs9396100 6:55367394 T ENSESTG00000000053 ENSESTT00000000149 Transcript intron_variant - - - - - - rs9396100 6:55367394 T CCDS43475.1 CCDS43475.1 Transcript intron_variant - - - - - - rs9396100 6:55367394 T ENSESTG00000000053 ENSESTT00000000148 Transcript intron_variant - - - - - - rs6459162 6:56353394 G ENSESTG00000012848 ENSESTT00000032282 Transcript upstream_gene_variant - - - - - - DISTANCE=1319 rs6459162 6:56353394 G CCDS47443.1 CCDS47443.1 Transcript intron_variant - - - - - - rs6459162 6:56353394 G 667 NM_015548.4 Transcript intron_variant - - - - - - rs6459162 6:56353394 G ENSESTG00000012848 ENSESTT00000032274 Transcript upstream_gene_variant - - - - - - DISTANCE=1319 rs2967961 6:56608598 A ENSESTG00000012777 ENSESTT00000032091 Transcript intron_variant - - - - - - rs2967961 6:56608598 A ENSESTG00000012777 ENSESTT00000032089 Transcript intron_variant - - - - - - rs2967961 6:56608598 A ENSESTG00000012777 ENSESTT00000032073 Transcript intron_variant - - - - - - rs2967961 6:56608598 A 100652766 XM_003403438.1 Transcript intron_variant - - - - - - rs2967961 6:56608598 A ENSESTG00000012777 ENSESTT00000032096 Transcript intron_variant - - - - - - rs2967961 6:56608598 A ENSESTG00000012777 ENSESTT00000032085 Transcript intron_variant - - - - - - rs3002012 6:56626355 A ENSESTG00000012777 ENSESTT00000032091 Transcript intron_variant - - - - - - rs3002012 6:56626355 A ENSESTG00000012777 ENSESTT00000032089 Transcript intron_variant - - - - - - rs3002012 6:56626355 A ENSESTG00000012777 ENSESTT00000032073 Transcript intron_variant - - - - - - rs3002012 6:56626355 A 100652766 XM_003403438.1 Transcript intron_variant - - - - - - rs3002012 6:56626355 A ENSESTG00000012777 ENSESTT00000032096 Transcript intron_variant - - - - - - rs3002012 6:56626355 A ENSESTG00000012777 ENSESTT00000032085 Transcript intron_variant - - - - - - rs9349871 6:57361831 G 100996481 XM_003846228.1 Transcript intron_variant - - - - - - rs9357978 6:57407430 G ENSESTG00000011289 ENSESTT00000028307 Transcript intron_variant - - - - - - rs9357978 6:57407430 G 100996481 XM_003846228.1 Transcript intron_variant - - - - - - rs4286787 6:57654987 T - - - intergenic_variant - - - - - - rs2996114 6:57758679 T - - - intergenic_variant - - - - - - rs3911739 6:58544991 C - - - intergenic_variant - - - - - - rs1761746 6:62665732 A CCDS4963.1 CCDS4963.1 Transcript intron_variant - - - - - - rs1761746 6:62665732 A 202559 NM_152688.2 Transcript intron_variant - - - - - - rs1761746 6:62665732 A ENSESTG00000035209 ENSESTT00000088945 Transcript intron_variant - - - - - - rs1761746 6:62665732 A ENSESTG00000035209 ENSESTT00000088948 Transcript intron_variant - - - - - - rs6455346 6:63012343 C - - - intergenic_variant - - - - - - rs2639436 6:63109332 G - - - intergenic_variant - - - - - - rs6453826 6:63569339 T - - - intergenic_variant - - - - - - rs2185579 6:63746131 G - - - intergenic_variant - - - - - - rs3003690 6:64775898 T 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs3003690 6:64775898 T CCDS47445.1 CCDS47445.1 Transcript intron_variant - - - - - - rs4710285 6:65519973 A 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs4710285 6:65519973 A CCDS47445.1 CCDS47445.1 Transcript intron_variant - - - - - - rs9363249 6:65527197 G 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs9363249 6:65527197 G CCDS47445.1 CCDS47445.1 Transcript intron_variant - - - - - - rs2350517 6:65764565 A 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs2350517 6:65764565 A CCDS47445.1 CCDS47445.1 Transcript intron_variant - - - - - - rs841533 6:65908427 G 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs841533 6:65908427 G CCDS47445.1 CCDS47445.1 Transcript intron_variant - - - - - - rs7773583 6:66104220 C CCDS4967.1 CCDS4967.1 Transcript intron_variant - - - - - - rs7773583 6:66104220 C 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs7773583 6:66104220 C CCDS47446.1 CCDS47446.1 Transcript intron_variant - - - - - - rs7773583 6:66104220 C 346007 NM_198283.1 Transcript intron_variant - - - - - - rs7773583 6:66104220 C 346007 NM_001142801.1 Transcript intron_variant - - - - - - rs7773583 6:66104220 C CCDS47445.1 CCDS47445.1 Transcript intron_variant - - - - - - rs9360134 6:66216990 C 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs9360134 6:66216990 C ENSESTG00000002021 ENSESTT00000005040 Transcript intron_variant - - - - - - rs9360134 6:66216990 C 346007 NM_001142801.1 Transcript intron_variant - - - - - - rs9360134 6:66216990 C ENSESTG00000002021 ENSESTT00000005036 Transcript intron_variant - - - - - - rs973299 6:66327030 G 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs973299 6:66327030 G ENSESTG00000002021 ENSESTT00000005040 Transcript intron_variant - - - - - - rs973299 6:66327030 G 346007 NM_001142801.1 Transcript intron_variant - - - - - - rs973299 6:66327030 G ENSESTG00000002021 ENSESTT00000005036 Transcript intron_variant - - - - - - rs6904116 6:66345939 T 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs6904116 6:66345939 T ENSESTG00000002021 ENSESTT00000005040 Transcript intron_variant - - - - - - rs6904116 6:66345939 T 346007 NM_001142801.1 Transcript intron_variant - - - - - - rs6904116 6:66345939 T ENSESTG00000002021 ENSESTT00000005036 Transcript intron_variant - - - - - - rs6907252 6:66383337 G 346007 NM_001142800.1 Transcript intron_variant - - - - - - rs6907252 6:66383337 G ENSESTG00000002021 ENSESTT00000005040 Transcript intron_variant - - - - - - rs6907252 6:66383337 G 346007 NM_001142801.1 Transcript intron_variant - - - - - - rs6907252 6:66383337 G ENSESTG00000002021 ENSESTT00000005036 Transcript intron_variant - - - - - - rs7770304 6:66462153 A - - - intergenic_variant - - - - - - rs1233113 6:66872425 T - - - intergenic_variant - - - - - - rs208511 6:66943860 G - - - intergenic_variant - - - - - - rs2214128 6:67049859 T - - - intergenic_variant - - - - - - rs9294695 6:67106269 G - - - intergenic_variant - - - - - - rs2816904 6:68380304 A - - - intergenic_variant - - - - - - rs4707521 6:68737921 A - - - intergenic_variant - - - - - - rs9342685 6:68799884 G - - - intergenic_variant - - - - - - rs777635 6:68813538 A - - - intergenic_variant - - - - - - rs777611 6:68819914 G - - - intergenic_variant - - - - - - rs1840497 6:68822971 G - - - intergenic_variant - - - - - - rs1083343 6:68845648 A - - - intergenic_variant - - - - - - rs2802709 6:69327269 A - - - intergenic_variant - - - - - - rs2785573 6:69728522 T CCDS4968.1 CCDS4968.1 Transcript intron_variant - - - - - - rs2785573 6:69728522 T 577 NM_001704.2 Transcript intron_variant - - - - - - rs2785573 6:69728522 T ENSESTG00000023196 ENSESTT00000058665 Transcript intron_variant - - - - - - rs314191 6:69800751 T CCDS4968.1 CCDS4968.1 Transcript intron_variant - - - - - - rs314191 6:69800751 T 577 NM_001704.2 Transcript intron_variant - - - - - - rs314196 6:69812668 T CCDS4968.1 CCDS4968.1 Transcript intron_variant - - - - - - rs314196 6:69812668 T 577 NM_001704.2 Transcript intron_variant - - - - - - rs1590251 6:69977370 T CCDS4968.1 CCDS4968.1 Transcript intron_variant - - - - - - rs1590251 6:69977370 T 577 NM_001704.2 Transcript intron_variant - - - - - - rs1590251 6:69977370 T ENSESTG00000023333 ENSESTT00000059077 Transcript intron_variant - - - - - - rs1590251 6:69977370 T ENSESTG00000023333 ENSESTT00000059050 Transcript intron_variant - - - - - - rs1743752 6:70212486 A - - - intergenic_variant - - - - - - rs636192 6:70897487 C CCDS4970.1 CCDS4970.1 Transcript intron_variant - - - - - - rs636192 6:70897487 C 1310 NM_001858.4 Transcript intron_variant - - - - - - rs6455395 6:71689520 C - - - intergenic_variant - - - - - - rs7773186 6:71694449 T - - - intergenic_variant - - - - - - rs6931996 6:71708260 C - - - intergenic_variant - - - - - - rs2347918 6:71718752 T - - - intergenic_variant - - - - - - rs9341325 6:72276883 T ENSESTG00000006651 ENSESTT00000016819 Transcript intron_variant - - - - - - rs844180 6:72356427 G ENSESTG00000006642 ENSESTT00000016797 Transcript intron_variant - - - - - - rs829270 6:72356448 A ENSESTG00000006642 ENSESTT00000016797 Transcript intron_variant - - - - - - rs2840988 6:72379054 T ENSESTG00000006642 ENSESTT00000016797 Transcript intron_variant - - - - - - rs829444 6:72387154 A ENSESTG00000006642 ENSESTT00000016797 Transcript intron_variant - - - - - - rs2840981 6:72400851 A ENSESTG00000006642 ENSESTT00000016797 Transcript intron_variant - - - - - - rs2224424 6:72407885 T ENSESTG00000006642 ENSESTT00000016797 Transcript intron_variant - - - - - - rs2254935 6:72409517 A ENSESTG00000006642 ENSESTT00000016797 Transcript intron_variant - - - - - - rs2840975 6:72418828 T ENSESTG00000006642 ENSESTT00000016797 Transcript intron_variant - - - - - - rs1204327 6:72423591 T ENSESTG00000006642 ENSESTT00000016797 Transcript intron_variant - - - - - - rs2348791 6:72563830 C - - - intergenic_variant - - - - - - rs6902486 6:72686733 A 22999 NM_014989.5 Transcript intron_variant - - - - - - rs6902486 6:72686733 A CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2449423 6:72785911 T 22999 NM_014989.5 Transcript intron_variant - - - - - - rs2449423 6:72785911 T CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2496553 6:72853057 A 22999 NM_014989.5 Transcript intron_variant - - - - - - rs2496553 6:72853057 A CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2463729 6:72893875 G 22999 NM_014989.5 Transcript intron_variant - - - - - - rs2463729 6:72893875 G ENSESTG00000014877 ENSESTT00000037243 Transcript intron_variant - - - - - - rs2463729 6:72893875 G CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2496521 6:72908447 C 22999 NM_014989.5 Transcript intron_variant - - - - - - rs2496521 6:72908447 C ENSESTG00000014877 ENSESTT00000037243 Transcript intron_variant - - - - - - rs2496521 6:72908447 C CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2697436 6:72934295 T 22999 NM_014989.5 Transcript intron_variant - - - - - - rs2697436 6:72934295 T 22999 NM_001168407.1 Transcript intron_variant - - - - - - rs2697436 6:72934295 T CCDS55031.1 CCDS55031.1 Transcript intron_variant - - - - - - rs2697436 6:72934295 T ENSESTG00000014877 ENSESTT00000037322 Transcript intron_variant - - - - - - rs2697436 6:72934295 T 22999 NM_001168409.1 Transcript intron_variant - - - - - - rs2697436 6:72934295 T ENSESTG00000014877 ENSESTT00000037338 Transcript intron_variant - - - - - - rs2697436 6:72934295 T ENSESTG00000014877 ENSESTT00000037313 Transcript intron_variant - - - - - - rs2697436 6:72934295 T ENSESTG00000014877 ENSESTT00000037330 Transcript intron_variant - - - - - - rs2697436 6:72934295 T ENSESTG00000014877 ENSESTT00000037243 Transcript intron_variant - - - - - - rs2697436 6:72934295 T CCDS55029.1 CCDS55029.1 Transcript intron_variant - - - - - - rs2697436 6:72934295 T CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2697436 6:72934295 T 22999 NM_001168410.1 Transcript intron_variant - - - - - - rs2697436 6:72934295 T 22999 NM_001168408.1 Transcript intron_variant - - - - - - rs2697436 6:72934295 T CCDS55030.1 CCDS55030.1 Transcript intron_variant - - - - - - rs2697436 6:72934295 T ENSESTG00000014877 ENSESTT00000037325 Transcript intron_variant - - - - - - rs2807502 6:72940332 A 22999 NM_014989.5 Transcript intron_variant - - - - - - rs2807502 6:72940332 A 22999 NM_001168407.1 Transcript intron_variant - - - - - - rs2807502 6:72940332 A CCDS55031.1 CCDS55031.1 Transcript intron_variant - - - - - - rs2807502 6:72940332 A ENSESTG00000014877 ENSESTT00000037322 Transcript intron_variant - - - - - - rs2807502 6:72940332 A 22999 NM_001168409.1 Transcript intron_variant - - - - - - rs2807502 6:72940332 A ENSESTG00000014877 ENSESTT00000037338 Transcript intron_variant - - - - - - rs2807502 6:72940332 A ENSESTG00000014877 ENSESTT00000037313 Transcript intron_variant - - - - - - rs2807502 6:72940332 A ENSESTG00000014877 ENSESTT00000037330 Transcript intron_variant - - - - - - rs2807502 6:72940332 A ENSESTG00000014877 ENSESTT00000037243 Transcript intron_variant - - - - - - rs2807502 6:72940332 A CCDS55029.1 CCDS55029.1 Transcript intron_variant - - - - - - rs2807502 6:72940332 A CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2807502 6:72940332 A 22999 NM_001168410.1 Transcript intron_variant - - - - - - rs2807502 6:72940332 A 22999 NM_001168408.1 Transcript intron_variant - - - - - - rs2807502 6:72940332 A CCDS55030.1 CCDS55030.1 Transcript intron_variant - - - - - - rs2807502 6:72940332 A ENSESTG00000014877 ENSESTT00000037325 Transcript intron_variant - - - - - - rs2697443 6:72945117 A 22999 NM_014989.5 Transcript intron_variant - - - - - - rs2697443 6:72945117 A 22999 NM_001168407.1 Transcript intron_variant - - - - - - rs2697443 6:72945117 A CCDS55032.1 CCDS55032.1 Transcript upstream_gene_variant - - - - - - DISTANCE=279 rs2697443 6:72945117 A 22999 NM_001168409.1 Transcript intron_variant - - - - - - rs2697443 6:72945117 A 22999 NM_001168408.1 Transcript intron_variant - - - - - - rs2697443 6:72945117 A CCDS55030.1 CCDS55030.1 Transcript intron_variant - - - - - - rs2697443 6:72945117 A ENSESTG00000014877 ENSESTT00000037325 Transcript intron_variant - - - - - - rs2697443 6:72945117 A ENSESTG00000014877 ENSESTT00000037322 Transcript intron_variant - - - - - - rs2697443 6:72945117 A CCDS55031.1 CCDS55031.1 Transcript intron_variant - - - - - - rs2697443 6:72945117 A ENSESTG00000014877 ENSESTT00000037338 Transcript intron_variant - - - - - - rs2697443 6:72945117 A ENSESTG00000014877 ENSESTT00000037313 Transcript intron_variant - - - - - - rs2697443 6:72945117 A ENSESTG00000014877 ENSESTT00000037330 Transcript intron_variant - - - - - - rs2697443 6:72945117 A ENSESTG00000014877 ENSESTT00000037243 Transcript intron_variant - - - - - - rs2697443 6:72945117 A CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2697443 6:72945117 A CCDS55029.1 CCDS55029.1 Transcript intron_variant - - - - - - rs2697443 6:72945117 A 22999 NM_001168410.1 Transcript intron_variant - - - - - - rs4504440 6:72984277 A 22999 NM_014989.5 Transcript intron_variant - - - - - - rs4504440 6:72984277 A 22999 NM_001168407.1 Transcript intron_variant - - - - - - rs4504440 6:72984277 A CCDS55032.1 CCDS55032.1 Transcript intron_variant - - - - - - rs4504440 6:72984277 A ENSESTG00000014877 ENSESTT00000037366 Transcript intron_variant - - - - - - rs4504440 6:72984277 A ENSESTG00000014877 ENSESTT00000037347 Transcript intron_variant - - - - - - rs4504440 6:72984277 A ENSESTG00000014877 ENSESTT00000037341 Transcript intron_variant - - - - - - rs4504440 6:72984277 A 22999 NM_001168409.1 Transcript intron_variant - - - - - - rs4504440 6:72984277 A 22999 NM_001168408.1 Transcript intron_variant - - - - - - rs4504440 6:72984277 A CCDS55030.1 CCDS55030.1 Transcript intron_variant - - - - - - rs4504440 6:72984277 A ENSESTG00000014877 ENSESTT00000037345 Transcript intron_variant - - - - - - rs4504440 6:72984277 A ENSESTG00000014877 ENSESTT00000037325 Transcript intron_variant - - - - - - rs4504440 6:72984277 A CCDS55031.1 CCDS55031.1 Transcript intron_variant - - - - - - rs4504440 6:72984277 A ENSESTG00000014877 ENSESTT00000037322 Transcript intron_variant - - - - - - rs4504440 6:72984277 A ENSESTG00000014877 ENSESTT00000037313 Transcript intron_variant - - - - - - rs4504440 6:72984277 A ENSESTG00000014877 ENSESTT00000037371 Transcript intron_variant - - - - - - rs4504440 6:72984277 A CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs4504440 6:72984277 A CCDS55029.1 CCDS55029.1 Transcript intron_variant - - - - - - rs4504440 6:72984277 A 22999 NM_001168410.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C 22999 NM_014989.5 Transcript intron_variant - - - - - - rs2789595 6:73096229 C 22999 NM_001168407.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C CCDS55032.1 CCDS55032.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C ENSESTG00000014877 ENSESTT00000037382 Transcript intron_variant - - - - - - rs2789595 6:73096229 C ENSESTG00000014877 ENSESTT00000037366 Transcript intron_variant - - - - - - rs2789595 6:73096229 C ENSESTG00000014877 ENSESTT00000037341 Transcript intron_variant - - - - - - rs2789595 6:73096229 C 22999 NM_001168409.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C 22999 NM_001168408.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C CCDS55030.1 CCDS55030.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C CCDS55031.1 CCDS55031.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C ENSESTG00000014877 ENSESTT00000037313 Transcript intron_variant - - - - - - rs2789595 6:73096229 C ENSESTG00000014877 ENSESTT00000037371 Transcript intron_variant - - - - - - rs2789595 6:73096229 C 22999 NM_001168411.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C CCDS55033.1 CCDS55033.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4124 rs2789595 6:73096229 C CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C CCDS55029.1 CCDS55029.1 Transcript intron_variant - - - - - - rs2789595 6:73096229 C 22999 NM_001168410.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T 22999 NM_014989.5 Transcript intron_variant - - - - - - rs2815740 6:73099101 T 22999 NM_001168407.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T CCDS55032.1 CCDS55032.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T ENSESTG00000014877 ENSESTT00000037382 Transcript intron_variant - - - - - - rs2815740 6:73099101 T ENSESTG00000014877 ENSESTT00000037366 Transcript intron_variant - - - - - - rs2815740 6:73099101 T ENSESTG00000014877 ENSESTT00000037341 Transcript intron_variant - - - - - - rs2815740 6:73099101 T 22999 NM_001168409.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T 22999 NM_001168408.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T CCDS55030.1 CCDS55030.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T CCDS55031.1 CCDS55031.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T ENSESTG00000014877 ENSESTT00000037313 Transcript intron_variant - - - - - - rs2815740 6:73099101 T ENSESTG00000014877 ENSESTT00000037371 Transcript intron_variant - - - - - - rs2815740 6:73099101 T 22999 NM_001168411.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T CCDS55033.1 CCDS55033.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1252 rs2815740 6:73099101 T CCDS47449.1 CCDS47449.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T CCDS55029.1 CCDS55029.1 Transcript intron_variant - - - - - - rs2815740 6:73099101 T 22999 NM_001168410.1 Transcript intron_variant - - - - - - rs3122370 6:73146842 A - - - intergenic_variant - - - - - - rs4706510 6:73424916 G 56479 NM_019842.3 Transcript intron_variant - - - - - - rs4706510 6:73424916 G 56479 NM_001160130.1 Transcript intron_variant - - - - - - rs4706510 6:73424916 G 56479 NM_001160132.1 Transcript intron_variant - - - - - - rs4706510 6:73424916 G CCDS55034.1 CCDS55034.1 Transcript intron_variant - - - - - - rs4706510 6:73424916 G CCDS55037.1 CCDS55037.1 Transcript intron_variant - - - - - - rs4706510 6:73424916 G CCDS55036.1 CCDS55036.1 Transcript intron_variant - - - - - - rs4706510 6:73424916 G CCDS4976.1 CCDS4976.1 Transcript intron_variant - - - - - - rs4706510 6:73424916 G 56479 NM_001160133.1 Transcript intron_variant - - - - - - rs4706510 6:73424916 G 56479 NM_001160134.1 Transcript intron_variant - - - - - - rs4706510 6:73424916 G CCDS55035.1 CCDS55035.1 Transcript intron_variant - - - - - - rs6453611 6:73637857 C 56479 NM_019842.3 Transcript intron_variant - - - - - - rs6453611 6:73637857 C 56479 NM_001160130.1 Transcript intron_variant - - - - - - rs6453611 6:73637857 C 56479 NM_001160132.1 Transcript intron_variant - - - - - - rs6453611 6:73637857 C CCDS55034.1 CCDS55034.1 Transcript intron_variant - - - - - - rs6453611 6:73637857 C CCDS55037.1 CCDS55037.1 Transcript intron_variant - - - - - - rs6453611 6:73637857 C CCDS55036.1 CCDS55036.1 Transcript intron_variant - - - - - - rs6453611 6:73637857 C CCDS4976.1 CCDS4976.1 Transcript intron_variant - - - - - - rs6453611 6:73637857 C 56479 NM_001160133.1 Transcript intron_variant - - - - - - rs6453611 6:73637857 C 56479 NM_001160134.1 Transcript intron_variant - - - - - - rs6453611 6:73637857 C CCDS55035.1 CCDS55035.1 Transcript intron_variant - - - - - - rs4708007 6:73669761 G - ENSR00001220307 RegulatoryFeature regulatory_region_variant - - - - - - rs4708007 6:73669761 G 56479 NM_019842.3 Transcript intron_variant - - - - - - rs4708007 6:73669761 G 56479 NM_001160130.1 Transcript intron_variant - - - - - - rs4708007 6:73669761 G 56479 NM_001160132.1 Transcript intron_variant - - - - - - rs4708007 6:73669761 G CCDS55034.1 CCDS55034.1 Transcript intron_variant - - - - - - rs4708007 6:73669761 G CCDS55037.1 CCDS55037.1 Transcript intron_variant - - - - - - rs4708007 6:73669761 G CCDS55036.1 CCDS55036.1 Transcript intron_variant - - - - - - rs4708007 6:73669761 G CCDS4976.1 CCDS4976.1 Transcript intron_variant - - - - - - rs4708007 6:73669761 G 56479 NM_001160133.1 Transcript intron_variant - - - - - - rs4708007 6:73669761 G 56479 NM_001160134.1 Transcript intron_variant - - - - - - rs4708007 6:73669761 G CCDS55035.1 CCDS55035.1 Transcript intron_variant - - - - - - rs7766570 6:74189574 A CCDS4979.1 CCDS4979.1 Transcript splice_region_variant,intron_variant - - - - - - rs7766570 6:74189574 A 25821 NM_133645.2 Transcript splice_region_variant,intron_variant - - - - - - rs7766570 6:74189574 A ENSESTG00000013120 ENSESTT00000032885 Transcript upstream_gene_variant - - - - - - DISTANCE=2270 rs7766570 6:74189574 A CCDS47452.1 CCDS47452.1 Transcript splice_region_variant,intron_variant - - - - - - rs7766570 6:74189574 A ENSESTG00000013100 ENSESTT00000032861 Transcript splice_region_variant,intron_variant - - - - - - rs7766570 6:74189574 A 25821 NM_012123.3 Transcript splice_region_variant,intron_variant - - - - - - rs7766570 6:74189574 A 25821 NM_001123226.1 Transcript splice_region_variant,intron_variant - - - - - - rs7766570 6:74189574 A ENSESTG00000013100 ENSESTT00000032859 Transcript splice_region_variant,intron_variant - - - - - - rs7766570 6:74189574 A CCDS34485.1 CCDS34485.1 Transcript splice_region_variant,intron_variant - - - - - - rs4485980 6:74716197 C - - - intergenic_variant - - - - - - rs915467 6:75028531 G - - - intergenic_variant - - - - - - rs1591588 6:75393357 C ENSESTG00000000994 ENSESTT00000002376 Transcript intron_variant - - - - - - rs1890092 6:75465458 G - - - intergenic_variant - - - - - - rs4708170 6:75732488 G - - - intergenic_variant - - - - - - rs600493 6:75824942 T 1303 NM_080645.2 Transcript intron_variant - - - - - - rs600493 6:75824942 T ENSESTG00000025938 ENSESTT00000065535 Transcript intron_variant - - - - - - rs600493 6:75824942 T CCDS43481.1 CCDS43481.1 Transcript intron_variant - - - - - - rs600493 6:75824942 T 1303 NM_004370.5 Transcript intron_variant - - - - - - rs600493 6:75824942 T CCDS43482.1 CCDS43482.1 Transcript intron_variant - - - - - - rs2064567 6:76004166 A 100506804 NR_040081.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2586 rs2064567 6:76004166 A ENSESTG00000025119 ENSESTT00000063388 Transcript intron_variant - - - - - - rs2064567 6:76004166 A ENSESTG00000025680 ENSESTT00000064778 Transcript downstream_gene_variant - - - - - - DISTANCE=1427 rs2064567 6:76004166 A ENSESTG00000025119 ENSESTT00000063379 Transcript intron_variant - - - - - - rs2842450 6:76105647 C ENSESTG00000025634 ENSESTT00000064699 Transcript intron_variant - - - - - - rs2842450 6:76105647 C 27145 NM_015687.2 Transcript intron_variant - - - - - - rs2842450 6:76105647 C CCDS4984.1 CCDS4984.1 Transcript intron_variant - - - - - - rs2703666 6:76145689 T ENSESTG00000025634 ENSESTT00000064699 Transcript intron_variant - - - - - - rs2703666 6:76145689 T 27145 NM_015687.2 Transcript intron_variant - - - - - - rs2998369 6:76187639 T ENSESTG00000025634 ENSESTT00000064705 Transcript intron_variant - - - - - - rs2998369 6:76187639 T ENSESTG00000025634 ENSESTT00000064699 Transcript intron_variant - - - - - - rs2998369 6:76187639 T 27145 NM_015687.2 Transcript intron_variant - - - - - - rs2185636 6:76737177 C ENSESTG00000019640 ENSESTT00000049297 Transcript intron_variant - - - - - - rs2185636 6:76737177 C 3617 NM_001563.2 Transcript intron_variant - - - - - - rs2185636 6:76737177 C CCDS4985.1 CCDS4985.1 Transcript intron_variant - - - - - - rs2872564 6:76985948 G - - - intergenic_variant - - - - - - rs2451584 6:77046576 C - - - intergenic_variant - - - - - - rs1457959 6:77340375 A - - - intergenic_variant - - - - - - rs6453950 6:77635301 A - - - intergenic_variant - - - - - - rs2575198 6:80213938 G 167691 NM_181714.3 Transcript intron_variant - - - - - - rs2575198 6:80213938 G 167691 NM_001122769.2 Transcript intron_variant - - - - - - rs2575198 6:80213938 G ENSESTG00000004060 ENSESTT00000010233 Transcript intron_variant - - - - - - rs2575198 6:80213938 G CCDS4990.1 CCDS4990.1 Transcript intron_variant - - - - - - rs1910598 6:80324360 A ENSESTG00000004060 ENSESTT00000010242 Transcript intron_variant - - - - - - rs1910598 6:80324360 A ENSESTG00000004060 ENSESTT00000010233 Transcript intron_variant - - - - - - rs1910598 6:80324360 A ENSESTG00000004060 ENSESTT00000010245 Transcript intron_variant - - - - - - rs700483 6:80631539 A ENSESTG00000021051 ENSESTT00000052917 Transcript downstream_gene_variant - - - - - - DISTANCE=3157 rs700483 6:80631539 A 6785 NM_022726.3 Transcript intron_variant - - - - - - rs700483 6:80631539 A CCDS4992.1 CCDS4992.1 Transcript intron_variant - - - - - - rs664145 6:80963677 A CCDS4994.1 CCDS4994.1 Transcript intron_variant - - - - - - rs664145 6:80963677 A ENSESTG00000020939 ENSESTT00000052724 Transcript intron_variant - - - - - - rs664145 6:80963677 A 594 NM_000056.3 Transcript intron_variant - - - - - - rs664145 6:80963677 A ENSESTG00000020939 ENSESTT00000052746 Transcript intron_variant - - - - - - rs664145 6:80963677 A 594 NM_183050.2 Transcript intron_variant - - - - - - rs517260 6:81199007 G - - - intergenic_variant - - - - - - rs571953 6:81223022 A - - - intergenic_variant - - - - - - rs6922376 6:81261665 A - ENSR00001221131 RegulatoryFeature regulatory_region_variant - - - - - - rs6922376 6:81261665 A - - - intergenic_variant - - - - - - rs1289388 6:81447462 A - - - intergenic_variant - - - - - - rs1017740 6:81536390 A - - - intergenic_variant - - - - - - rs1539307 6:82772327 T - - - intergenic_variant - - - - - - rs9344263 6:82965443 G - - - intergenic_variant - - - - - - rs3011886 6:83135315 C - - - intergenic_variant - - - - - - rs287835 6:83431458 G - - - intergenic_variant - - - - - - rs52481 6:83609832 T ENSESTG00000023563 ENSESTT00000059520 Transcript intron_variant - - - - - - rs52481 6:83609832 T CCDS34491.1 CCDS34491.1 Transcript intron_variant - - - - - - rs52481 6:83609832 T 90025 NM_198920.1 Transcript intron_variant - - - - - - rs3118921 6:83696934 T ENSESTG00000023563 ENSESTT00000059520 Transcript intron_variant - - - - - - rs3118921 6:83696934 T CCDS34491.1 CCDS34491.1 Transcript intron_variant - - - - - - rs3118921 6:83696934 T 90025 NM_198920.1 Transcript intron_variant - - - - - - rs4455637 6:83754094 C ENSESTG00000023563 ENSESTT00000059520 Transcript intron_variant - - - - - - rs4455637 6:83754094 C CCDS34491.1 CCDS34491.1 Transcript intron_variant - - - - - - rs4455637 6:83754094 C 90025 NM_198920.1 Transcript intron_variant - - - - - - rs4455637 6:83754094 C ENSESTG00000023563 ENSESTT00000059440 Transcript intron_variant - - - - - - rs1180245 6:83920884 G CCDS34492.1 CCDS34492.1 Transcript downstream_gene_variant - - - - - - DISTANCE=759 rs1180245 6:83920884 G ENSESTG00000023473 ENSESTT00000059272 Transcript downstream_gene_variant - - - - - - DISTANCE=510 rs1180245 6:83920884 G 4199 NM_002395.4 Transcript 3_prime_UTR_variant 2743 - - - - - rs2324417 6:84115257 T ENSESTG00000023408 ENSESTT00000059150 Transcript intron_variant - - - - - - rs2324417 6:84115257 T CCDS34492.1 CCDS34492.1 Transcript intron_variant - - - - - - rs2324417 6:84115257 T 4199 NM_002395.4 Transcript intron_variant - - - - - - rs217306 6:84370487 T 9892 NM_014841.2 Transcript intron_variant - - - - - - rs217306 6:84370487 T ENSESTG00000023212 ENSESTT00000058752 Transcript intron_variant - - - - - - rs217306 6:84370487 T ENSESTG00000023212 ENSESTT00000058847 Transcript downstream_gene_variant - - - - - - DISTANCE=1578 rs217306 6:84370487 T 9892 NM_001242793.1 Transcript intron_variant - - - - - - rs217306 6:84370487 T 9892 NM_001256718.1 Transcript intron_variant - - - - - - rs217306 6:84370487 T 9892 NM_001242794.1 Transcript intron_variant - - - - - - rs217306 6:84370487 T 9892 NM_001256717.1 Transcript intron_variant - - - - - - rs217306 6:84370487 T CCDS47455.1 CCDS47455.1 Transcript intron_variant - - - - - - rs217306 6:84370487 T ENSESTG00000023212 ENSESTT00000058850 Transcript intron_variant - - - - - - rs217306 6:84370487 T CCDS56437.1 CCDS56437.1 Transcript intron_variant - - - - - - rs217306 6:84370487 T ENSESTG00000023212 ENSESTT00000058809 Transcript intron_variant - - - - - - rs217306 6:84370487 T 9892 NM_001242792.1 Transcript intron_variant - - - - - - rs217306 6:84370487 T ENSESTG00000023212 ENSESTT00000058831 Transcript intron_variant - - - - - - rs217306 6:84370487 T CCDS56438.1 CCDS56438.1 Transcript intron_variant - - - - - - rs217284 6:84411886 A - ENSR00001221445 RegulatoryFeature regulatory_region_variant - - - - - - rs217284 6:84411886 A 9892 NM_014841.2 Transcript intron_variant - - - - - - rs217284 6:84411886 A ENSESTG00000023212 ENSESTT00000058752 Transcript intron_variant - - - - - - rs217284 6:84411886 A ENSESTG00000023212 ENSESTT00000058847 Transcript intron_variant - - - - - - rs217284 6:84411886 A 9892 NM_001242793.1 Transcript intron_variant - - - - - - rs217284 6:84411886 A 9892 NM_001256718.1 Transcript intron_variant - - - - - - rs217284 6:84411886 A ENSESTG00000023212 ENSESTT00000058783 Transcript intron_variant - - - - - - rs217284 6:84411886 A 9892 NM_001242794.1 Transcript intron_variant - - - - - - rs217284 6:84411886 A 9892 NM_001256717.1 Transcript intron_variant - - - - - - rs217284 6:84411886 A CCDS47455.1 CCDS47455.1 Transcript intron_variant - - - - - - rs217284 6:84411886 A ENSESTG00000023212 ENSESTT00000058850 Transcript intron_variant - - - - - - rs217284 6:84411886 A CCDS56437.1 CCDS56437.1 Transcript intron_variant - - - - - - rs217284 6:84411886 A ENSESTG00000023212 ENSESTT00000058809 Transcript intron_variant - - - - - - rs217284 6:84411886 A 9892 NM_001242792.1 Transcript intron_variant - - - - - - rs217284 6:84411886 A ENSESTG00000023212 ENSESTT00000058831 Transcript intron_variant - - - - - - rs217284 6:84411886 A CCDS56438.1 CCDS56438.1 Transcript intron_variant - - - - - - rs7762104 6:86314990 C 10492 NM_001159674.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2512 rs7762104 6:86314990 C 10492 NM_001253771.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2512 rs7762104 6:86314990 C 10492 NM_001159673.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2512 rs7762104 6:86314990 C 10492 NM_001159677.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2512 rs7762104 6:86314990 C 10492 NM_001159676.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2512 rs2816553 6:86985367 G - - - intergenic_variant - - - - - - rs9342108 6:87976548 C 23036 NM_015021.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3142 rs6454633 6:88291556 T ENSESTG00000031295 ENSESTT00000079248 Transcript intron_variant - - - - - - rs6454633 6:88291556 T ENSESTG00000031295 ENSESTT00000079166 Transcript intron_variant - - - - - - rs6454633 6:88291556 T CCDS5011.1 CCDS5011.1 Transcript intron_variant - - - - - - rs6454633 6:88291556 T ENSESTG00000031295 ENSESTT00000079178 Transcript intron_variant - - - - - - rs6454633 6:88291556 T 57038 NM_020320.3 Transcript intron_variant - - - - - - rs2763284 6:88508481 G - ENSR00001221894 RegulatoryFeature regulatory_region_variant - - - - - - rs2763284 6:88508481 G - - - intergenic_variant - - - - - - rs269420 6:88749610 T - - - intergenic_variant - - - - - - rs563825 6:88750154 T - - - intergenic_variant - - - - - - rs1359423 6:88946270 A ENSESTG00000010951 ENSESTT00000027433 Transcript intron_variant - - - - - - rs6415026 6:89221216 T - - - intergenic_variant - - - - - - rs4707515 6:89803596 G - ENSR00001222053 RegulatoryFeature regulatory_region_variant - - - - - - rs4707515 6:89803596 G 135295 NM_080743.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2082 rs4707515 6:89803596 G ENSESTG00000021203 ENSESTT00000053336 Transcript downstream_gene_variant - - - - - - DISTANCE=4976 rs4707515 6:89803596 G CCDS47459.1 CCDS47459.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4701 rs1311730 6:91451302 T - - - intergenic_variant - - - - - - rs711270 6:91584052 G - - - intergenic_variant - - - - - - rs1145783 6:91618443 A - - - intergenic_variant - - - - - - rs527844 6:92394187 G ENSESTG00000025584 ENSESTT00000064498 Transcript downstream_gene_variant - - - - - - DISTANCE=1809 rs728184 6:92465630 G - - - intergenic_variant - - - - - - rs6918177 6:92615806 C - - - intergenic_variant - - - - - - rs370515 6:93953850 T ENSESTG00000034480 ENSESTT00000087212 Transcript intron_variant - - - - - - rs370515 6:93953850 T CCDS5031.1 CCDS5031.1 Transcript intron_variant - - - - - - rs370515 6:93953850 T 2045 NM_004440.3 Transcript intron_variant - - - - - - rs4707800 6:94201509 T - - - intergenic_variant - - - - - - rs2875657 6:94547425 G - - - intergenic_variant - - - - - - rs1488308 6:94675319 A - - - intergenic_variant - - - - - - rs611033 6:94739043 C - - - intergenic_variant - - - - - - rs660360 6:94752791 T - - - intergenic_variant - - - - - - rs374211 6:95058766 A - - - intergenic_variant - - - - - - rs377668 6:95100639 T - - - intergenic_variant - - - - - - rs6454997 6:95144208 C - - - intergenic_variant - - - - - - rs222566 6:95221943 G - - - intergenic_variant - - - - - - rs794674 6:95475009 A - - - intergenic_variant - - - - - - rs28492025 6:95830775 A - - - intergenic_variant - - - - - - rs2716055 6:95840636 G - - - intergenic_variant - - - - - - rs2926779 6:95843902 T - - - intergenic_variant - - - - - - rs2716090 6:95852015 G - - - intergenic_variant - - - - - - rs2613536 6:95863897 C - - - intergenic_variant - - - - - - rs2613538 6:95866043 A - - - intergenic_variant - - - - - - rs2716086 6:95867463 A - - - intergenic_variant - - - - - - rs2613539 6:95869200 T - - - intergenic_variant - - - - - - rs2613540 6:95869839 C - - - intergenic_variant - - - - - - rs2380223 6:95887464 A - - - intergenic_variant - - - - - - rs2251658 6:95889994 T - - - intergenic_variant - - - - - - rs2613564 6:95892904 T - - - intergenic_variant - - - - - - rs2613570 6:95933789 C - - - intergenic_variant - - - - - - rs7449598 6:95938972 C - - - intergenic_variant - - - - - - rs9372170 6:95953449 A - - - intergenic_variant - - - - - - rs9374839 6:96073031 T - - - intergenic_variant - - - - - - rs4348323 6:96079733 A - - - intergenic_variant - - - - - - rs6907090 6:96090396 C - - - intergenic_variant - - - - - - rs4645428 6:96092853 A - - - intergenic_variant - - - - - - rs9375312 6:96116562 A - - - intergenic_variant - - - - - - rs6923305 6:96154133 T - - - intergenic_variant - - - - - - rs4298353 6:96624057 T ENSESTG00000012410 ENSESTT00000031099 Transcript intron_variant - - - - - - rs4298353 6:96624057 T 10690 NM_006581.3 Transcript intron_variant - - - - - - rs972109 6:96826787 C - - - intergenic_variant - - - - - - rs4839836 6:96899584 T - - - intergenic_variant - - - - - - rs6924435 6:97299719 G - - - intergenic_variant - - - - - - rs2482410 6:97721567 A CCDS5039.1 CCDS5039.1 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047738 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047648 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047786 Transcript upstream_gene_variant - - - - - - DISTANCE=890 rs2482410 6:97721567 A 253714 NM_198468.2 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047765 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047734 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047756 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047748 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047703 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047661 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047720 Transcript intron_variant - - - - - - rs2482410 6:97721567 A ENSESTG00000018824 ENSESTT00000047683 Transcript intron_variant - - - - - - rs1676006 6:97794288 A - - - intergenic_variant - - - - - - rs1033607 6:98170859 A - - - intergenic_variant - - - - - - rs2503786 6:98500168 T - - - intergenic_variant - - - - - - rs2505055 6:98501680 G - - - intergenic_variant - - - - - - rs2503785 6:98503528 T - - - intergenic_variant - - - - - - rs1828076 6:98710910 G - - - intergenic_variant - - - - - - rs6569387 6:98734600 G ENSESTG00000000123 ENSESTT00000000317 Transcript intron_variant - - - - - - rs6569405 6:98766998 A ENSESTG00000000123 ENSESTT00000000317 Transcript intron_variant - - - - - - rs9398774 6:98780864 G ENSESTG00000000123 ENSESTT00000000317 Transcript intron_variant - - - - - - rs906464 6:98784636 T ENSESTG00000000123 ENSESTT00000000317 Transcript intron_variant - - - - - - rs9388617 6:99081719 T - ENSR00001497904 RegulatoryFeature regulatory_region_variant - - - - - - rs9388617 6:99081719 T - - - intergenic_variant - - - - - - rs6916460 6:99086464 T - - - intergenic_variant - - - - - - rs4240563 6:99143313 G - - - intergenic_variant - - - - - - rs9321161 6:99212243 C - - - intergenic_variant - - - - - - rs2397681 6:100373584 C CCDS5044.1 CCDS5044.1 Transcript intron_variant - - - - - - rs2397681 6:100373584 C 84539 NM_032503.2 Transcript intron_variant - - - - - - rs2397681 6:100373584 C 84539 NM_001040179.1 Transcript intron_variant - - - - - - rs6925660 6:100512343 A 728012 NR_038384.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6925660 6:100512343 A ENSESTG00000033110 ENSESTT00000083661 Transcript intron_variant - - - - - - rs6925660 6:100512343 A ENSESTG00000033110 ENSESTT00000083659 Transcript intron_variant - - - - - - rs6925660 6:100512343 A ENSESTG00000033110 ENSESTT00000083677 Transcript intron_variant - - - - - - rs2503098 6:100608036 A - - - intergenic_variant - - - - - - rs2658148 6:100766443 T - - - intergenic_variant - - - - - - rs6918572 6:100928167 G - - - intergenic_variant - - - - - - rs2213596 6:100935878 G - - - intergenic_variant - - - - - - rs9404019 6:101195321 T ENSESTG00000031384 ENSESTT00000079170 Transcript intron_variant - - - - - - rs9404019 6:101195321 T CCDS5046.1 CCDS5046.1 Transcript intron_variant - - - - - - rs9404019 6:101195321 T 10973 NM_006828.2 Transcript intron_variant - - - - - - rs7763656 6:101211398 G ENSESTG00000031384 ENSESTT00000079170 Transcript intron_variant - - - - - - rs7763656 6:101211398 G CCDS5046.1 CCDS5046.1 Transcript intron_variant - - - - - - rs7763656 6:101211398 G 10973 NM_006828.2 Transcript intron_variant - - - - - - rs2852491 6:101787554 C - - - intergenic_variant - - - - - - rs2518180 6:101834048 C - - - intergenic_variant - - - - - - rs2788272 6:101883773 A 2898 NM_001166247.1 Transcript intron_variant - - - - - - rs2788272 6:101883773 A CCDS5049.1 CCDS5049.1 Transcript intron_variant - - - - - - rs2788272 6:101883773 A CCDS55045.1 CCDS55045.1 Transcript intron_variant - - - - - - rs2788272 6:101883773 A 2898 NM_021956.4 Transcript intron_variant - - - - - - rs2788272 6:101883773 A CCDS5048.1 CCDS5048.1 Transcript intron_variant - - - - - - rs2788272 6:101883773 A 2898 NM_175768.3 Transcript intron_variant - - - - - - rs2518257 6:101980667 T 2898 NM_001166247.1 Transcript intron_variant - - - - - - rs2518257 6:101980667 T CCDS5049.1 CCDS5049.1 Transcript intron_variant - - - - - - rs2518257 6:101980667 T CCDS55045.1 CCDS55045.1 Transcript intron_variant - - - - - - rs2518257 6:101980667 T 2898 NM_021956.4 Transcript intron_variant - - - - - - rs2518257 6:101980667 T CCDS5048.1 CCDS5048.1 Transcript intron_variant - - - - - - rs2518257 6:101980667 T 2898 NM_175768.3 Transcript intron_variant - - - - - - rs949396 6:101999657 T 2898 NM_001166247.1 Transcript intron_variant - - - - - - rs949396 6:101999657 T CCDS5049.1 CCDS5049.1 Transcript intron_variant - - - - - - rs949396 6:101999657 T CCDS55045.1 CCDS55045.1 Transcript intron_variant - - - - - - rs949396 6:101999657 T 2898 NM_021956.4 Transcript intron_variant - - - - - - rs949396 6:101999657 T CCDS5048.1 CCDS5048.1 Transcript intron_variant - - - - - - rs949396 6:101999657 T 2898 NM_175768.3 Transcript intron_variant - - - - - - rs2852579 6:102015969 A 2898 NM_001166247.1 Transcript intron_variant - - - - - - rs2852579 6:102015969 A CCDS5049.1 CCDS5049.1 Transcript intron_variant - - - - - - rs2852579 6:102015969 A CCDS55045.1 CCDS55045.1 Transcript intron_variant - - - - - - rs2852579 6:102015969 A 2898 NM_021956.4 Transcript intron_variant - - - - - - rs2852579 6:102015969 A CCDS5048.1 CCDS5048.1 Transcript intron_variant - - - - - - rs2852579 6:102015969 A 2898 NM_175768.3 Transcript intron_variant - - - - - - rs2852580 6:102016049 A 2898 NM_001166247.1 Transcript intron_variant - - - - - - rs2852580 6:102016049 A CCDS5049.1 CCDS5049.1 Transcript intron_variant - - - - - - rs2852580 6:102016049 A CCDS55045.1 CCDS55045.1 Transcript intron_variant - - - - - - rs2852580 6:102016049 A 2898 NM_021956.4 Transcript intron_variant - - - - - - rs2852580 6:102016049 A CCDS5048.1 CCDS5048.1 Transcript intron_variant - - - - - - rs2852580 6:102016049 A 2898 NM_175768.3 Transcript intron_variant - - - - - - rs2256978 6:102025906 A 2898 NM_001166247.1 Transcript intron_variant - - - - - - rs2256978 6:102025906 A CCDS5049.1 CCDS5049.1 Transcript intron_variant - - - - - - rs2256978 6:102025906 A CCDS55045.1 CCDS55045.1 Transcript intron_variant - - - - - - rs2256978 6:102025906 A 2898 NM_021956.4 Transcript intron_variant - - - - - - rs2256978 6:102025906 A CCDS5048.1 CCDS5048.1 Transcript intron_variant - - - - - - rs2256978 6:102025906 A 2898 NM_175768.3 Transcript intron_variant - - - - - - rs2749068 6:102035580 A 2898 NM_001166247.1 Transcript intron_variant - - - - - - rs2749068 6:102035580 A CCDS5049.1 CCDS5049.1 Transcript intron_variant - - - - - - rs2749068 6:102035580 A CCDS55045.1 CCDS55045.1 Transcript intron_variant - - - - - - rs2749068 6:102035580 A 2898 NM_021956.4 Transcript intron_variant - - - - - - rs2749068 6:102035580 A CCDS5048.1 CCDS5048.1 Transcript intron_variant - - - - - - rs2749068 6:102035580 A 2898 NM_175768.3 Transcript intron_variant - - - - - - rs2749067 6:102035697 A 2898 NM_001166247.1 Transcript intron_variant - - - - - - rs2749067 6:102035697 A CCDS5049.1 CCDS5049.1 Transcript intron_variant - - - - - - rs2749067 6:102035697 A CCDS55045.1 CCDS55045.1 Transcript intron_variant - - - - - - rs2749067 6:102035697 A 2898 NM_021956.4 Transcript intron_variant - - - - - - rs2749067 6:102035697 A CCDS5048.1 CCDS5048.1 Transcript intron_variant - - - - - - rs2749067 6:102035697 A 2898 NM_175768.3 Transcript intron_variant - - - - - - rs949393 6:102098491 C - ENSR00001498045 RegulatoryFeature regulatory_region_variant - - - - - - rs949393 6:102098491 C 2898 NM_001166247.1 Transcript intron_variant - - - - - - rs949393 6:102098491 C CCDS55045.1 CCDS55045.1 Transcript intron_variant - - - - - - rs949393 6:102098491 C ENSESTG00000014788 ENSESTT00000037080 Transcript intron_variant - - - - - - rs949393 6:102098491 C 2898 NM_021956.4 Transcript intron_variant - - - - - - rs949393 6:102098491 C CCDS5048.1 CCDS5048.1 Transcript intron_variant - - - - - - rs949393 6:102098491 C CCDS5049.1 CCDS5049.1 Transcript intron_variant - - - - - - rs949393 6:102098491 C 2898 NM_175768.3 Transcript intron_variant - - - - - - rs949393 6:102098491 C ENSESTG00000014788 ENSESTT00000037073 Transcript intron_variant - - - - - - rs4273696 6:102756839 A - - - intergenic_variant - - - - - - rs6928441 6:102887273 G - - - intergenic_variant - - - - - - rs9404219 6:103038816 C - - - intergenic_variant - - - - - - rs9404233 6:103151709 T - - - intergenic_variant - - - - - - rs559841 6:103617463 C - - - intergenic_variant - - - - - - rs7753285 6:103797337 A - - - intergenic_variant - - - - - - rs2506725 6:103926390 G ENSESTG00000014667 ENSESTT00000036698 Transcript intron_variant - - - - - - rs9404432 6:104035074 C ENSESTG00000014667 ENSESTT00000036698 Transcript intron_variant - - - - - - rs4947189 6:104084535 T - - - intergenic_variant - - - - - - rs4476861 6:104255388 C - - - intergenic_variant - - - - - - rs6907116 6:104380260 C - - - intergenic_variant - - - - - - rs7768225 6:105140484 C - - - intergenic_variant - - - - - - rs1149292 6:105650803 C - - - intergenic_variant - - - - - - rs2157457 6:106081390 C - - - intergenic_variant - - - - - - rs4945730 6:106270065 C - - - intergenic_variant - - - - - - rs4437514 6:106417203 T - - - intergenic_variant - - - - - - rs803529 6:106835538 C ENSESTG00000006796 ENSESTT00000017285 Transcript intron_variant - - - - - - rs2353593 6:106852582 G ENSESTG00000006796 ENSESTT00000017285 Transcript intron_variant - - - - - - rs9400028 6:107014524 C - ENSR00001223588 RegulatoryFeature regulatory_region_variant - - - - - - rs9400028 6:107014524 C ENSESTG00000006840 ENSESTT00000017466 Transcript intron_variant - - - - - - rs9400028 6:107014524 C ENSESTG00000006840 ENSESTT00000017454 Transcript downstream_gene_variant - - - - - - DISTANCE=2166 rs9400028 6:107014524 C ENSESTG00000006840 ENSESTT00000017449 Transcript intron_variant - - - - - - rs9400028 6:107014524 C ENSESTG00000006840 ENSESTT00000017468 Transcript downstream_gene_variant - - - - - - DISTANCE=2166 rs9400028 6:107014524 C CCDS34506.1 CCDS34506.1 Transcript intron_variant - - - - - - rs9400028 6:107014524 C 202 NM_001624.2 Transcript intron_variant - - - - - - rs9400028 6:107014524 C 84816 NM_032730.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4379 rs9386575 6:107061216 C CCDS5056.1 CCDS5056.1 Transcript intron_variant - - - - - - rs9386575 6:107061216 C ENSESTG00000007140 ENSESTT00000018024 Transcript intron_variant - - - - - - rs9386575 6:107061216 C 84816 NM_032730.4 Transcript intron_variant - - - - - - rs9386575 6:107061216 C ENSESTG00000007140 ENSESTT00000018028 Transcript intron_variant - - - - - - rs1665922 6:107317946 G - - - intergenic_variant - - - - - - rs2593792 6:107324172 G - - - intergenic_variant - - - - - - rs311242 6:107333691 G - - - intergenic_variant - - - - - - rs6909688 6:107356332 C CCDS5058.1 CCDS5058.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4633 rs6909688 6:107356332 C 51250 NM_001142470.1 Transcript intron_variant - - - - - - rs6909688 6:107356332 C 51250 NM_016487.3 Transcript intron_variant - - - - - - rs6909688 6:107356332 C 51250 NM_001142468.1 Transcript intron_variant - - - - - - rs6909688 6:107356332 C ENSESTG00000007067 ENSESTT00000017897 Transcript intron_variant - - - - - - rs6909688 6:107356332 C CCDS55046.1 CCDS55046.1 Transcript intron_variant - - - - - - rs7774237 6:107502125 T ENSESTG00000024144 ENSESTT00000061080 Transcript intron_variant - - - - - - rs7774237 6:107502125 T 57107 NM_020381.3 Transcript intron_variant - - - - - - rs7774237 6:107502125 T ENSESTG00000024144 ENSESTT00000061130 Transcript intron_variant - - - - - - rs7774237 6:107502125 T CCDS5059.1 CCDS5059.1 Transcript intron_variant - - - - - - rs7774237 6:107502125 T ENSESTG00000024144 ENSESTT00000061123 Transcript intron_variant - - - - - - rs7774237 6:107502125 T ENSESTG00000024144 ENSESTT00000061075 Transcript intron_variant - - - - - - rs2474911 6:107810545 A - ENSR00001223767 RegulatoryFeature regulatory_region_variant - - - - - - rs2474911 6:107810545 A ENSESTG00000023769 ENSESTT00000059983 Transcript upstream_gene_variant - - - - - - DISTANCE=1043 rs2474911 6:107810545 A ENSESTG00000024144 ENSESTT00000061080 Transcript intron_variant - - - - - - rs2474911 6:107810545 A ENSESTG00000023769 ENSESTT00000059995 Transcript upstream_gene_variant - - - - - - DISTANCE=1043 rs2474911 6:107810545 A 55084 NM_018013.3 Transcript upstream_gene_variant - - - - - - DISTANCE=772 rs2474911 6:107810545 A ENSESTG00000023769 ENSESTT00000059986 Transcript upstream_gene_variant - - - - - - DISTANCE=1043 rs2474911 6:107810545 A ENSESTG00000024144 ENSESTT00000061075 Transcript intron_variant - - - - - - rs2474911 6:107810545 A CCDS43488.1 CCDS43488.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1276 rs718192 6:107948926 T ENSESTG00000023769 ENSESTT00000059983 Transcript intron_variant - - - - - - rs718192 6:107948926 T ENSESTG00000023769 ENSESTT00000060003 Transcript intron_variant - - - - - - rs718192 6:107948926 T 55084 NM_018013.3 Transcript intron_variant - - - - - - rs718192 6:107948926 T CCDS43488.1 CCDS43488.1 Transcript intron_variant - - - - - - rs2354096 6:108090139 T 256380 NM_198081.3 Transcript intron_variant - - - - - - rs2354096 6:108090139 T ENSESTG00000024076 ENSESTT00000060900 Transcript intron_variant - - - - - - rs2354096 6:108090139 T ENSESTG00000024076 ENSESTT00000060883 Transcript intron_variant - - - - - - rs2354096 6:108090139 T ENSESTG00000024076 ENSESTT00000060848 Transcript intron_variant - - - - - - rs2354096 6:108090139 T ENSESTG00000024076 ENSESTT00000060923 Transcript intron_variant - - - - - - rs2354096 6:108090139 T ENSESTG00000024076 ENSESTT00000060864 Transcript intron_variant - - - - - - rs2354096 6:108090139 T CCDS5060.2 CCDS5060.2 Transcript intron_variant - - - - - - rs1878779 6:108094199 A 256380 NM_198081.3 Transcript intron_variant - - - - - - rs1878779 6:108094199 A ENSESTG00000024076 ENSESTT00000060900 Transcript intron_variant - - - - - - rs1878779 6:108094199 A ENSESTG00000024076 ENSESTT00000060883 Transcript intron_variant - - - - - - rs1878779 6:108094199 A ENSESTG00000024076 ENSESTT00000060848 Transcript intron_variant - - - - - - rs1878779 6:108094199 A ENSESTG00000024076 ENSESTT00000060923 Transcript upstream_gene_variant - - - - - - DISTANCE=744 rs1878779 6:108094199 A ENSESTG00000024076 ENSESTT00000060864 Transcript intron_variant - - - - - - rs1878779 6:108094199 A CCDS5060.2 CCDS5060.2 Transcript upstream_gene_variant - - - - - - DISTANCE=668 rs938973 6:108102677 C 256380 NM_198081.3 Transcript intron_variant - - - - - - rs938973 6:108102677 C ENSESTG00000024076 ENSESTT00000060900 Transcript intron_variant - - - - - - rs938973 6:108102677 C ENSESTG00000024076 ENSESTT00000060883 Transcript intron_variant - - - - - - rs938973 6:108102677 C ENSESTG00000024076 ENSESTT00000060848 Transcript intron_variant - - - - - - rs938973 6:108102677 C ENSESTG00000024076 ENSESTT00000060864 Transcript intron_variant - - - - - - rs9372169 6:108120252 G 256380 NM_198081.3 Transcript intron_variant - - - - - - rs9372169 6:108120252 G ENSESTG00000024076 ENSESTT00000060900 Transcript intron_variant - - - - - - rs9372169 6:108120252 G ENSESTG00000024076 ENSESTT00000060883 Transcript intron_variant - - - - - - rs9372169 6:108120252 G ENSESTG00000024076 ENSESTT00000060848 Transcript intron_variant - - - - - - rs9372169 6:108120252 G ENSESTG00000024076 ENSESTT00000060864 Transcript intron_variant - - - - - - rs938969 6:108153528 C - - - intergenic_variant - - - - - - rs4945808 6:108438270 G - - - intergenic_variant - - - - - - rs566790 6:108593989 T - - - intergenic_variant - - - - - - rs9480860 6:108821525 T CCDS5067.1 CCDS5067.1 Transcript intron_variant - - - - - - rs9480860 6:108821525 T ENSESTG00000015801 ENSESTT00000039673 Transcript intron_variant - - - - - - rs9480860 6:108821525 T 246269 NM_145315.3 Transcript intron_variant - - - - - - rs4946931 6:108961003 T 2309 NM_201559.2 Transcript intron_variant - - - - - - rs4946931 6:108961003 T 2309 NM_001455.3 Transcript intron_variant - - - - - - rs4946931 6:108961003 T CCDS5068.1 CCDS5068.1 Transcript intron_variant - - - - - - rs4946931 6:108961003 T ENSESTG00000015926 ENSESTT00000039932 Transcript intron_variant - - - - - - rs4946931 6:108961003 T ENSESTG00000015926 ENSESTT00000039939 Transcript intron_variant - - - - - - rs4946931 6:108961003 T ENSESTG00000015926 ENSESTT00000039943 Transcript intron_variant - - - - - - rs4946931 6:108961003 T ENSESTG00000015926 ENSESTT00000039937 Transcript intron_variant - - - - - - rs2768544 6:109162612 C - ENSR00001498469 RegulatoryFeature regulatory_region_variant - - - - - - rs2768544 6:109162612 C - - - intergenic_variant - - - - - - rs352838 6:109518697 T 389422 XM_003403515.2 Transcript intron_variant - - - - - - rs352838 6:109518697 T ENSESTG00000027104 ENSESTT00000068332 Transcript downstream_gene_variant - - - - - - DISTANCE=886 rs352838 6:109518697 T ENSESTG00000027104 ENSESTT00000068322 Transcript intron_variant - - - - - - rs352836 6:109526086 G - ENSR00001498513 RegulatoryFeature regulatory_region_variant - - - - - - rs352836 6:109526086 G 389422 XM_003403515.2 Transcript intron_variant - - - - - - rs352836 6:109526086 G ENSESTG00000027124 ENSESTT00000068347 Transcript upstream_gene_variant - - - - - - DISTANCE=1478 rs7742191 6:110214298 C - ENSR00001498569 RegulatoryFeature regulatory_region_variant - - - - - - rs7742191 6:110214298 C - - - intergenic_variant - - - - - - rs4451177 6:110215617 G - - - intergenic_variant - - - - - - rs2905293 6:110794423 C CCDS5084.1 CCDS5084.1 Transcript intron_variant - - - - - - rs2905293 6:110794423 C 85413 NM_033125.3 Transcript intron_variant - - - - - - rs4945886 6:111943679 G - - - intergenic_variant - - - - - - rs2673310 6:112330810 G - - - intergenic_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086463 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086452 Transcript intron_variant - - - - - - rs9387064 6:112562575 A CCDS43491.1 CCDS43491.1 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086476 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086473 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086485 Transcript intron_variant - - - - - - rs9387064 6:112562575 A CCDS34514.1 CCDS34514.1 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086450 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086478 Transcript intron_variant - - - - - - rs9387064 6:112562575 A 3910 NM_001105206.2 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034132 ENSESTT00000086265 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086490 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086457 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086493 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086435 Transcript intron_variant - - - - - - rs9387064 6:112562575 A 3910 NM_002290.4 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086444 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086460 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086492 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086468 Transcript intron_variant - - - - - - rs9387064 6:112562575 A ENSESTG00000034162 ENSESTT00000086488 Transcript intron_variant - - - - - - rs9387064 6:112562575 A 3910 NM_001105207.2 Transcript intron_variant - - - - - - rs947714 6:112782339 T - - - intergenic_variant - - - - - - rs827088 6:113348251 G - - - intergenic_variant - - - - - - rs9320426 6:113378416 A - - - intergenic_variant - - - - - - rs9942544 6:113714743 C - - - intergenic_variant - - - - - - rs9400669 6:114086539 C 100652953 XM_003403517.1 Transcript intron_variant - - - - - - rs2810175 6:114124403 G ENSESTG00000030882 ENSESTT00000077770 Transcript intron_variant - - - - - - rs2810175 6:114124403 G 100652953 XM_003403517.1 Transcript intron_variant - - - - - - rs2492887 6:114546415 C ENSESTG00000030778 ENSESTT00000077548 Transcript intron_variant - - - - - - rs2492887 6:114546415 C ENSESTG00000030804 ENSESTT00000077583 Transcript intron_variant - - - - - - rs2492887 6:114546415 C ENSESTG00000018502 ENSESTT00000046580 Transcript upstream_gene_variant - - - - - - DISTANCE=4897 rs2183751 6:115605376 A - - - intergenic_variant - - - - - - rs2213813 6:115888543 C - - - intergenic_variant - - - - - - rs1204828 6:116566138 A CCDS5104.1 CCDS5104.1 Transcript downstream_gene_variant - - - - - - DISTANCE=951 rs1204828 6:116566138 A ENSESTG00000009937 ENSESTT00000024872 Transcript downstream_gene_variant - - - - - - DISTANCE=751 rs1204828 6:116566138 A 221294 NM_152729.2 Transcript 3_prime_UTR_variant 2414 - - - - - rs1204828 6:116566138 A 23270 NM_021648.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4989 rs1204828 6:116566138 A ENSESTG00000010106 ENSESTT00000025290 Transcript intron_variant - - - - - - rs1150108 6:117045674 G 3841 NM_002269.2 Transcript intron_variant - - - - - - rs1150108 6:117045674 G ENSESTG00000010031 ENSESTT00000025138 Transcript intron_variant - - - - - - rs1150108 6:117045674 G CCDS5111.1 CCDS5111.1 Transcript intron_variant - - - - - - rs2095283 6:117654711 C CCDS5116.1 CCDS5116.1 Transcript intron_variant - - - - - - rs2095283 6:117654711 C 6098 NM_002944.2 Transcript intron_variant - - - - - - rs210650 6:117853264 G - ENSR00001225415 RegulatoryFeature regulatory_region_variant - - - - - - rs210650 6:117853264 G CCDS34522.1 CCDS34522.1 Transcript intron_variant - - - - - - rs210650 6:117853264 G ENSESTG00000009862 ENSESTT00000024707 Transcript upstream_gene_variant - - - - - - DISTANCE=4980 rs210650 6:117853264 G ENSESTG00000009862 ENSESTT00000024693 Transcript intron_variant - - - - - - rs210650 6:117853264 G ENSESTG00000009862 ENSESTT00000024703 Transcript intron_variant - - - - - - rs210650 6:117853264 G 285761 NM_173674.1 Transcript intron_variant - - - - - - rs210650 6:117853264 G ENSESTG00000009862 ENSESTT00000024701 Transcript intron_variant - - - - - - rs210650 6:117853264 G ENSESTG00000009862 ENSESTT00000024698 Transcript intron_variant - - - - - - rs2760235 6:118237687 G CCDS34524.1 CCDS34524.1 Transcript intron_variant - - - - - - rs2760235 6:118237687 G 222553 NM_001029858.3 Transcript intron_variant - - - - - - rs6569025 6:118970004 C ENSESTG00000034868 ENSESTT00000088148 Transcript upstream_gene_variant - - - - - - DISTANCE=1754 rs6569025 6:118970004 C ENSESTG00000034868 ENSESTT00000088145 Transcript intron_variant - - - - - - rs6569025 6:118970004 C ENSESTG00000034868 ENSESTT00000088138 Transcript intron_variant - - - - - - rs6569025 6:118970004 C 387119 NM_001042475.2 Transcript intron_variant - - - - - - rs6569025 6:118970004 C CCDS43498.1 CCDS43498.1 Transcript intron_variant - - - - - - rs6569025 6:118970004 C CCDS55052.1 CCDS55052.1 Transcript intron_variant - - - - - - rs6569025 6:118970004 C ENSESTG00000034868 ENSESTT00000088144 Transcript intron_variant - - - - - - rs6569025 6:118970004 C CCDS5119.2 CCDS5119.2 Transcript intron_variant - - - - - - rs6569025 6:118970004 C 387119 NM_001178035.1 Transcript intron_variant - - - - - - rs6569025 6:118970004 C ENSESTG00000034868 ENSESTT00000088147 Transcript upstream_gene_variant - - - - - - DISTANCE=1726 rs6569025 6:118970004 C ENSESTG00000034868 ENSESTT00000088141 Transcript intron_variant - - - - - - rs6569025 6:118970004 C 387119 NM_206921.2 Transcript intron_variant - - - - - - rs6931217 6:119878779 T - ENSR00001225715 RegulatoryFeature regulatory_region_variant - - - - - - rs6931217 6:119878779 T - - - intergenic_variant - - - - - - rs1772598 6:119997735 T - - - intergenic_variant - - - - - - rs3013682 6:120643292 C - - - intergenic_variant - - - - - - rs7759123 6:120850754 A - - - intergenic_variant - - - - - - rs6569170 6:121268531 A - - - intergenic_variant - - - - - - rs1273735 6:121453924 A CCDS43501.1 CCDS43501.1 Transcript intron_variant - - - - - - rs1273735 6:121453924 A ENSESTG00000024921 ENSESTT00000062921 Transcript upstream_gene_variant - - - - - - DISTANCE=1066 rs1273735 6:121453924 A 221322 NM_152730.4 Transcript intron_variant - - - - - - rs1273744 6:121464139 C CCDS43501.1 CCDS43501.1 Transcript intron_variant - - - - - - rs1273744 6:121464139 C 221322 NM_152730.4 Transcript intron_variant - - - - - - rs6938933 6:121614002 T CCDS43501.1 CCDS43501.1 Transcript intron_variant - - - - - - rs6938933 6:121614002 T ENSESTG00000024848 ENSESTT00000062888 Transcript intron_variant - - - - - - rs6938933 6:121614002 T 221322 NM_152730.4 Transcript intron_variant - - - - - - rs1041097 6:121671606 T - - - intergenic_variant - - - - - - rs4413648 6:122010571 G - - - intergenic_variant - - - - - - rs3013779 6:122244759 T - - - intergenic_variant - - - - - - rs2816117 6:122371506 A - - - intergenic_variant - - - - - - rs2816090 6:122400875 T - - - intergenic_variant - - - - - - rs2606657 6:122475144 A - - - intergenic_variant - - - - - - rs804479 6:122740000 A CCDS47470.1 CCDS47470.1 Transcript intron_variant - - - - - - rs804479 6:122740000 A ENSESTG00000033298 ENSESTT00000084202 Transcript intron_variant - - - - - - rs804479 6:122740000 A 3298 NM_004506.3 Transcript intron_variant - - - - - - rs804479 6:122740000 A ENSESTG00000033298 ENSESTT00000084197 Transcript intron_variant - - - - - - rs804479 6:122740000 A CCDS5124.1 CCDS5124.1 Transcript intron_variant - - - - - - rs804479 6:122740000 A 3298 NM_001243094.1 Transcript intron_variant - - - - - - rs804479 6:122740000 A 3298 NM_001135564.1 Transcript intron_variant - - - - - - rs7383274 6:123159196 G - - - intergenic_variant - - - - - - rs6569340 6:123693514 A ENSESTG00000030659 ENSESTT00000077249 Transcript intron_variant - - - - - - rs6569340 6:123693514 A CCDS55053.1 CCDS55053.1 Transcript intron_variant - - - - - - rs6569340 6:123693514 A 10345 NM_001251987.1 Transcript intron_variant - - - - - - rs6569340 6:123693514 A 10345 NM_006073.3 Transcript intron_variant - - - - - - rs234479 6:124360136 G CCDS34526.1 CCDS34526.1 Transcript intron_variant - - - - - - rs234479 6:124360136 G 154215 NM_001040214.1 Transcript intron_variant - - - - - - rs234479 6:124360136 G 154215 NM_153355.3 Transcript intron_variant - - - - - - rs699377 6:124527169 T CCDS34526.1 CCDS34526.1 Transcript intron_variant - - - - - - rs699377 6:124527169 T 154215 NM_001040214.1 Transcript intron_variant - - - - - - rs699377 6:124527169 T 154215 NM_153355.3 Transcript intron_variant - - - - - - rs802498 6:124587027 G CCDS34526.1 CCDS34526.1 Transcript intron_variant - - - - - - rs802498 6:124587027 G 154215 NM_001040214.1 Transcript intron_variant - - - - - - rs802498 6:124587027 G 154215 NM_153355.3 Transcript intron_variant - - - - - - rs332599 6:124742989 G CCDS34526.1 CCDS34526.1 Transcript intron_variant - - - - - - rs332599 6:124742989 G 154215 NM_001040214.1 Transcript intron_variant - - - - - - rs332599 6:124742989 G 154215 NM_153355.3 Transcript intron_variant - - - - - - rs6915265 6:125280670 G ENSESTG00000034618 ENSESTT00000087554 Transcript intron_variant - - - - - - rs6915265 6:125280670 G 7955 NR_026876.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6915265 6:125280670 G ENSESTG00000034618 ENSESTT00000087548 Transcript intron_variant - - - - - - rs6915265 6:125280670 G ENSESTG00000034599 ENSESTT00000087514 Transcript upstream_gene_variant - - - - - - DISTANCE=3192 rs6915265 6:125280670 G ENSESTG00000034618 ENSESTT00000087560 Transcript intron_variant - - - - - - rs1819641 6:126703731 A - - - intergenic_variant - - - - - - rs853967 6:127038518 T - ENSR00001226439 RegulatoryFeature regulatory_region_variant - - - - - - rs853967 6:127038518 T - - - intergenic_variant - - - - - - rs994495 6:127450254 T CCDS5135.1 CCDS5135.1 Transcript intron_variant - - - - - - rs994495 6:127450254 T ENSESTG00000008798 ENSESTT00000022120 Transcript intron_variant - - - - - - rs994495 6:127450254 T ENSESTG00000008798 ENSESTT00000022115 Transcript intron_variant - - - - - - rs994495 6:127450254 T 84870 NM_032784.3 Transcript intron_variant - - - - - - rs994495 6:127450254 T ENSESTG00000008798 ENSESTT00000022127 Transcript intron_variant - - - - - - rs938151 6:127904667 G 352999 NM_001010905.1 Transcript intron_variant - - - - - - rs938151 6:127904667 G CCDS34533.1 CCDS34533.1 Transcript intron_variant - - - - - - rs445508 6:128197404 C CCDS34534.1 CCDS34534.1 Transcript intron_variant - - - - - - rs445508 6:128197404 C 387357 NM_001010923.2 Transcript intron_variant - - - - - - rs445508 6:128197404 C 387357 NM_001164687.1 Transcript intron_variant - - - - - - rs445508 6:128197404 C 387357 NM_001164685.1 Transcript intron_variant - - - - - - rs445508 6:128197404 C ENSESTG00000008843 ENSESTT00000022197 Transcript intron_variant - - - - - - rs445508 6:128197404 C CCDS55056.1 CCDS55056.1 Transcript intron_variant - - - - - - rs5018187 6:128405781 G CCDS5137.1 CCDS5137.1 Transcript intron_variant - - - - - - rs5018187 6:128405781 G 5796 NM_001135648.1 Transcript intron_variant - - - - - - rs5018187 6:128405781 G 5796 NM_002844.3 Transcript intron_variant - - - - - - rs5018187 6:128405781 G ENSESTG00000008832 ENSESTT00000022161 Transcript upstream_gene_variant - - - - - - DISTANCE=2009 rs5018187 6:128405781 G CCDS47473.1 CCDS47473.1 Transcript intron_variant - - - - - - rs6569524 6:128414945 T CCDS5137.1 CCDS5137.1 Transcript intron_variant - - - - - - rs6569524 6:128414945 T 5796 NM_001135648.1 Transcript intron_variant - - - - - - rs6569524 6:128414945 T 5796 NM_002844.3 Transcript intron_variant - - - - - - rs6569524 6:128414945 T CCDS47473.1 CCDS47473.1 Transcript intron_variant - - - - - - rs1738294 6:128599902 A CCDS5137.1 CCDS5137.1 Transcript intron_variant - - - - - - rs1738294 6:128599902 A 5796 NM_001135648.1 Transcript intron_variant - - - - - - rs1738294 6:128599902 A 5796 NM_002844.3 Transcript intron_variant - - - - - - rs1738294 6:128599902 A CCDS47473.1 CCDS47473.1 Transcript intron_variant - - - - - - rs1768344 6:128611984 A CCDS5137.1 CCDS5137.1 Transcript intron_variant - - - - - - rs1768344 6:128611984 A 5796 NM_001135648.1 Transcript intron_variant - - - - - - rs1768344 6:128611984 A 5796 NM_002844.3 Transcript intron_variant - - - - - - rs1768344 6:128611984 A CCDS47473.1 CCDS47473.1 Transcript intron_variant - - - - - - rs2784891 6:129775972 G ENSESTG00000007203 ENSESTT00000018188 Transcript upstream_gene_variant - - - - - - DISTANCE=1505 rs2784891 6:129775972 G CCDS5138.1 CCDS5138.1 Transcript intron_variant - - - - - - rs2784891 6:129775972 G 3908 NM_000426.3 Transcript intron_variant - - - - - - rs2784891 6:129775972 G 3908 NM_001079823.1 Transcript intron_variant - - - - - - rs2784891 6:129775972 G ENSESTG00000007195 ENSESTT00000018148 Transcript downstream_gene_variant - - - - - - DISTANCE=1694 rs2039686 6:130251906 C - - - intergenic_variant - - - - - - rs6569649 6:130356026 A - ENSR00001226874 RegulatoryFeature regulatory_region_variant - - - - - - rs6569649 6:130356026 A 84456 NM_032438.2 Transcript intron_variant - - - - - - rs6569649 6:130356026 A ENSESTG00000021614 ENSESTT00000054413 Transcript intron_variant - - - - - - rs6569649 6:130356026 A ENSESTG00000021614 ENSESTT00000054391 Transcript intron_variant - - - - - - rs6569649 6:130356026 A 84456 NM_001007102.2 Transcript intron_variant - - - - - - rs6569649 6:130356026 A ENSESTG00000021614 ENSESTT00000054416 Transcript intron_variant - - - - - - rs159877 6:130686546 G - ENSR00001499870 RegulatoryFeature regulatory_region_variant - - - - - - rs159877 6:130686546 G 114801 NM_001258277.1 Transcript upstream_gene_variant - - - - - - DISTANCE=880 rs159877 6:130686546 G ENSESTG00000021717 ENSESTT00000054550 Transcript upstream_gene_variant - - - - - - DISTANCE=984 rs159877 6:130686546 G 154075 NM_001258275.1 Transcript 5_prime_UTR_variant 25 - - - - - rs159877 6:130686546 G 114801 NM_001258276.1 Transcript upstream_gene_variant - - - - - - DISTANCE=880 rs9375812 6:131668231 C - - - intergenic_variant - - - - - - rs2749925 6:131931605 A 9439 NM_004830.3 Transcript intron_variant - - - - - - rs2749925 6:131931605 A CCDS59039.1 CCDS59039.1 Transcript intron_variant - - - - - - rs2749925 6:131931605 A ENSESTG00000017308 ENSESTT00000043690 Transcript intron_variant - - - - - - rs2749925 6:131931605 A CCDS5147.1 CCDS5147.1 Transcript intron_variant - - - - - - rs2749925 6:131931605 A 9439 NM_001270521.1 Transcript intron_variant - - - - - - rs2749925 6:131931605 A CCDS5146.1 CCDS5146.1 Transcript intron_variant - - - - - - rs2749925 6:131931605 A 9439 NM_015979.3 Transcript intron_variant - - - - - - rs2749925 6:131931605 A 9439 NM_001270522.1 Transcript intron_variant - - - - - - rs2749925 6:131931605 A ENSESTG00000017308 ENSESTT00000043703 Transcript intron_variant - - - - - - rs2876170 6:132412313 C ENSESTG00000032948 ENSESTT00000083260 Transcript intron_variant - - - - - - rs2876170 6:132412313 C ENSESTG00000032948 ENSESTT00000083255 Transcript intron_variant - - - - - - rs1406938 6:132493117 C 100507254 NR_038981.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2603 rs1406938 6:132493117 C ENSESTG00000032954 ENSESTT00000083279 Transcript downstream_gene_variant - - - - - - DISTANCE=2618 rs2050732 6:132713111 G - ENSR00001500074 RegulatoryFeature regulatory_region_variant - - - - - - rs2050732 6:132713111 G CCDS5152.2 CCDS5152.2 Transcript intron_variant - - - - - - rs2050732 6:132713111 G ENSESTG00000033090 ENSESTT00000083687 Transcript intron_variant - - - - - - rs2050732 6:132713111 G 26002 NM_015529.2 Transcript intron_variant - - - - - - rs2842893 6:132813879 A 8417 NM_003569.2 Transcript intron_variant - - - - - - rs2842893 6:132813879 A CCDS5153.1 CCDS5153.1 Transcript intron_variant - - - - - - rs2842893 6:132813879 A ENSESTG00000033033 ENSESTT00000083558 Transcript intron_variant - - - - - - rs2842893 6:132813879 A ENSESTG00000033033 ENSESTT00000083602 Transcript intron_variant - - - - - - rs2840831 6:132866240 C - - - intergenic_variant - - - - - - rs1230741 6:133215845 A - - - intergenic_variant - - - - - - rs535048 6:133218611 T - - - intergenic_variant - - - - - - rs6569868 6:133472156 G - - - intergenic_variant - - - - - - rs508368 6:133509754 A - - - intergenic_variant - - - - - - rs212814 6:133708418 A CCDS43506.1 CCDS43506.1 Transcript intron_variant - - - - - - rs212814 6:133708418 A 2070 NM_172105.3 Transcript intron_variant - - - - - - rs212814 6:133708418 A ENSESTG00000027477 ENSESTT00000069279 Transcript intron_variant - - - - - - rs212814 6:133708418 A ENSESTG00000027477 ENSESTT00000069241 Transcript intron_variant - - - - - - rs212814 6:133708418 A CCDS5166.1 CCDS5166.1 Transcript intron_variant - - - - - - rs212814 6:133708418 A 2070 NM_172103.3 Transcript intron_variant - - - - - - rs212814 6:133708418 A CCDS5165.1 CCDS5165.1 Transcript intron_variant - - - - - - rs212814 6:133708418 A ENSESTG00000027477 ENSESTT00000069258 Transcript downstream_gene_variant - - - - - - DISTANCE=4838 rs212814 6:133708418 A ENSESTG00000027477 ENSESTT00000069225 Transcript intron_variant - - - - - - rs212814 6:133708418 A 2070 NM_004100.4 Transcript intron_variant - - - - - - rs126403 6:133761696 C CCDS43506.1 CCDS43506.1 Transcript intron_variant - - - - - - rs126403 6:133761696 C 2070 NM_172105.3 Transcript intron_variant - - - - - - rs126403 6:133761696 C ENSESTG00000027477 ENSESTT00000069279 Transcript intron_variant - - - - - - rs126403 6:133761696 C ENSESTG00000027477 ENSESTT00000069241 Transcript intron_variant - - - - - - rs126403 6:133761696 C CCDS5166.1 CCDS5166.1 Transcript intron_variant - - - - - - rs126403 6:133761696 C 2070 NM_172103.3 Transcript intron_variant - - - - - - rs126403 6:133761696 C CCDS5165.1 CCDS5165.1 Transcript intron_variant - - - - - - rs126403 6:133761696 C ENSESTG00000027703 ENSESTT00000069740 Transcript upstream_gene_variant - - - - - - DISTANCE=1091 rs126403 6:133761696 C ENSESTG00000027477 ENSESTT00000069225 Transcript intron_variant - - - - - - rs126403 6:133761696 C 2070 NM_004100.4 Transcript intron_variant - - - - - - rs9483585 6:133851207 A CCDS43506.1 CCDS43506.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1264 rs9483585 6:133851207 A CCDS5166.1 CCDS5166.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1264 rs9483585 6:133851207 A CCDS5165.1 CCDS5165.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1264 rs9483585 6:133851207 A 2070 NM_172105.3 Transcript 3_prime_UTR_variant 3642 - - - - - rs9483585 6:133851207 A 2070 NM_172103.3 Transcript 3_prime_UTR_variant 3573 - - - - - rs9483585 6:133851207 A 2070 NM_004100.4 Transcript 3_prime_UTR_variant 3642 - - - - - rs1208278 6:134170148 A 154089 NR_027030.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1208278 6:134170148 A ENSESTG00000027530 ENSESTT00000069298 Transcript intron_variant - - - - - - rs1208278 6:134170148 A ENSESTG00000027629 ENSESTT00000069561 Transcript intron_variant - - - - - - rs1208278 6:134170148 A ENSESTG00000027629 ENSESTT00000069585 Transcript intron_variant - - - - - - rs1208230 6:134183230 T ENSESTG00000027629 ENSESTT00000069561 Transcript intron_variant - - - - - - rs1208230 6:134183230 T ENSESTG00000027629 ENSESTT00000069585 Transcript intron_variant - - - - - - rs2327432 6:134214096 C - ENSR00001227524 RegulatoryFeature regulatory_region_variant - - - - - - rs2327432 6:134214096 C CCDS5167.1 CCDS5167.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1156 rs2327432 6:134214096 C ENSESTG00000027667 ENSESTT00000069631 Transcript upstream_gene_variant - - - - - - DISTANCE=1202 rs2327432 6:134214096 C 6943 NM_198392.2 Transcript intron_variant - - - - - - rs2327432 6:134214096 C ENSESTG00000027537 ENSESTT00000069345 Transcript downstream_gene_variant - - - - - - DISTANCE=705 rs2327432 6:134214096 C ENSESTG00000027629 ENSESTT00000069561 Transcript intron_variant - - - - - - rs2327432 6:134214096 C ENSESTG00000027629 ENSESTT00000069565 Transcript upstream_gene_variant - - - - - - DISTANCE=3952 rs2327432 6:134214096 C ENSESTG00000027629 ENSESTT00000069585 Transcript upstream_gene_variant - - - - - - DISTANCE=3976 rs2327432 6:134214096 C 6943 NM_003206.3 Transcript downstream_gene_variant - - - - - - DISTANCE=701 rs229909 6:134274224 G - ENSR00001500198 RegulatoryFeature regulatory_region_variant - - - - - - rs229909 6:134274224 G ENSESTG00000027556 ENSESTT00000069472 Transcript intron_variant - - - - - - rs229909 6:134274224 G ENSESTG00000027556 ENSESTT00000069506 Transcript upstream_gene_variant - - - - - - DISTANCE=78 rs229909 6:134274224 G 9519 NM_001253676.1 Transcript intron_variant - - - - - - rs229909 6:134274224 G 9519 NM_004865.3 Transcript upstream_gene_variant - - - - - - DISTANCE=77 rs229909 6:134274224 G ENSESTG00000027629 ENSESTT00000069561 Transcript upstream_gene_variant - - - - - - DISTANCE=40 rs229909 6:134274224 G ENSESTG00000027556 ENSESTT00000069534 Transcript upstream_gene_variant - - - - - - DISTANCE=78 rs1540938 6:134521006 G - ENSR00001227607 RegulatoryFeature regulatory_region_variant - - - - - - rs1540938 6:134521006 G 6446 NM_001143676.1 Transcript intron_variant - - - - - - rs1540938 6:134521006 G ENSESTG00000014749 ENSESTT00000036905 Transcript intron_variant - - - - - - rs1540938 6:134521006 G CCDS47476.1 CCDS47476.1 Transcript intron_variant - - - - - - rs4895448 6:135796450 T - ENSR00001500339 RegulatoryFeature regulatory_region_variant - - - - - - rs4895448 6:135796450 T ENSESTG00000014158 ENSESTT00000035425 Transcript intron_variant - - - - - - rs4895448 6:135796450 T 54806 NM_017651.4 Transcript intron_variant - - - - - - rs4895448 6:135796450 T 54806 NM_001134831.1 Transcript intron_variant - - - - - - rs4895448 6:135796450 T 54806 NM_001134832.1 Transcript intron_variant - - - - - - rs4895448 6:135796450 T CCDS47484.1 CCDS47484.1 Transcript intron_variant - - - - - - rs4895448 6:135796450 T CCDS47483.1 CCDS47483.1 Transcript intron_variant - - - - - - rs4895448 6:135796450 T ENSESTG00000014158 ENSESTT00000035403 Transcript intron_variant - - - - - - rs4895448 6:135796450 T 54806 NM_001134830.1 Transcript intron_variant - - - - - - rs4895448 6:135796450 T ENSESTG00000014158 ENSESTT00000035420 Transcript intron_variant - - - - - - rs1418596 6:137298260 C - - - intergenic_variant - - - - - - rs276506 6:137357127 T 53832 NM_014432.2 Transcript intron_variant - - - - - - rs276506 6:137357127 T CCDS5181.1 CCDS5181.1 Transcript intron_variant - - - - - - rs276506 6:137357127 T ENSESTG00000015080 ENSESTT00000037808 Transcript intron_variant - - - - - - rs276506 6:137357127 T ENSESTG00000015080 ENSESTT00000037781 Transcript intron_variant - - - - - - rs276473 6:137456234 T - - - intergenic_variant - - - - - - rs2785236 6:137950498 C - - - intergenic_variant - - - - - - rs1145970 6:138517322 C ENSESTG00000019079 ENSESTT00000048016 Transcript intron_variant - - - - - - rs1145970 6:138517322 C CCDS5189.2 CCDS5189.2 Transcript intron_variant - - - - - - rs1145970 6:138517322 C 57221 NM_020340.4 Transcript intron_variant - - - - - - rs9321703 6:139464513 G 51696 NM_016217.2 Transcript intron_variant - - - - - - rs9321703 6:139464513 G CCDS5194.1 CCDS5194.1 Transcript intron_variant - - - - - - rs201278 6:140498444 A - - - intergenic_variant - - - - - - rs552046 6:140518695 T - - - intergenic_variant - - - - - - rs1996618 6:140527407 G 100500879 NR_037441.1 Transcript downstream_gene_variant - - - - - - DISTANCE=944 rs6932853 6:140705094 G - - - intergenic_variant - - - - - - rs2328063 6:140714797 A - ENSR00001229011 RegulatoryFeature regulatory_region_variant - - - - - - rs2328063 6:140714797 A - - - intergenic_variant - - - - - - rs3850222 6:140778946 T - - - intergenic_variant - - - - - - rs9373279 6:140782752 C - - - intergenic_variant - - - - - - rs9399319 6:140809775 A - - - intergenic_variant - - - - - - rs2050814 6:140828151 G - - - intergenic_variant - - - - - - rs9376521 6:140836136 A - - - intergenic_variant - - - - - - rs1932698 6:140836928 G - - - intergenic_variant - - - - - - rs928712 6:140886302 G - - - intergenic_variant - - - - - - rs9484518 6:141850928 C - - - intergenic_variant - - - - - - rs6920157 6:142187492 G ENSESTG00000031274 ENSESTT00000078859 Transcript intron_variant - - - - - - rs225597 6:142447864 T - - - intergenic_variant - - - - - - rs225681 6:142521306 T ENSESTG00000005687 ENSESTT00000014496 Transcript intron_variant - - - - - - rs225681 6:142521306 T 51534 NM_016485.3 Transcript intron_variant - - - - - - rs225681 6:142521306 T ENSESTG00000005687 ENSESTT00000014485 Transcript downstream_gene_variant - - - - - - DISTANCE=1392 rs225681 6:142521306 T CCDS5197.1 CCDS5197.1 Transcript intron_variant - - - - - - rs198677 6:143194771 A 3097 NM_006734.3 Transcript intron_variant - - - - - - rs198677 6:143194771 A ENSESTG00000005802 ENSESTT00000014705 Transcript intron_variant - - - - - - rs198677 6:143194771 A ENSESTG00000005802 ENSESTT00000014701 Transcript intron_variant - - - - - - rs198685 6:143204244 T - ENSR00001229329 RegulatoryFeature regulatory_region_variant - - - - - - rs198685 6:143204244 T 3097 NM_006734.3 Transcript intron_variant - - - - - - rs198685 6:143204244 T ENSESTG00000005802 ENSESTT00000014705 Transcript intron_variant - - - - - - rs198685 6:143204244 T ENSESTG00000005802 ENSESTT00000014701 Transcript intron_variant - - - - - - rs200150 6:143409668 G ENSESTG00000031389 ENSESTT00000079327 Transcript intron_variant - - - - - - rs200150 6:143409668 G ENSESTG00000031389 ENSESTT00000079297 Transcript intron_variant - - - - - - rs200150 6:143409668 G CCDS5198.1 CCDS5198.1 Transcript intron_variant - - - - - - rs200150 6:143409668 G ENSESTG00000031389 ENSESTT00000079319 Transcript intron_variant - - - - - - rs200150 6:143409668 G 51390 NM_016108.2 Transcript intron_variant - - - - - - rs200150 6:143409668 G ENSESTG00000031389 ENSESTT00000079333 Transcript intron_variant - - - - - - rs200150 6:143409668 G ENSESTG00000031389 ENSESTT00000079224 Transcript intron_variant - - - - - - rs200150 6:143409668 G ENSESTG00000031389 ENSESTT00000079338 Transcript intron_variant - - - - - - rs7760969 6:143854957 G - - - intergenic_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079936 Transcript intron_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079929 Transcript intron_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079898 Transcript intron_variant - - - - - - rs2262450 6:144014275 C CCDS43512.1 CCDS43512.1 Transcript intron_variant - - - - - - rs2262450 6:144014275 C CCDS47492.1 CCDS47492.1 Transcript intron_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079875 Transcript intron_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079913 Transcript intron_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079905 Transcript intron_variant - - - - - - rs2262450 6:144014275 C CCDS47493.1 CCDS47493.1 Transcript intron_variant - - - - - - rs2262450 6:144014275 C CCDS47494.1 CCDS47494.1 Transcript intron_variant - - - - - - rs2262450 6:144014275 C 9749 NM_001100164.1 Transcript intron_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079925 Transcript intron_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079946 Transcript intron_variant - - - - - - rs2262450 6:144014275 C 9749 NM_001100165.1 Transcript intron_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079893 Transcript intron_variant - - - - - - rs2262450 6:144014275 C 9749 NM_001100166.1 Transcript intron_variant - - - - - - rs2262450 6:144014275 C ENSESTG00000031634 ENSESTT00000079907 Transcript intron_variant - - - - - - rs2262450 6:144014275 C 9749 NM_014721.2 Transcript intron_variant - - - - - - rs7753306 6:144208674 C CCDS47495.1 CCDS47495.1 Transcript intron_variant - - - - - - rs7753306 6:144208674 C ENSESTG00000031634 ENSESTT00000080170 Transcript intron_variant - - - - - - rs7753306 6:144208674 C 153918 NM_001013623.2 Transcript intron_variant - - - - - - rs7753306 6:144208674 C ENSESTG00000031634 ENSESTT00000080099 Transcript downstream_gene_variant - - - - - - DISTANCE=3171 rs2328541 6:144370691 G ENSESTG00000035139 ENSESTT00000088808 Transcript intron_variant - - - - - - rs2328541 6:144370691 G ENSESTG00000035139 ENSESTT00000088802 Transcript intron_variant - - - - - - rs2328541 6:144370691 G ENSESTG00000035139 ENSESTT00000088799 Transcript intron_variant - - - - - - rs2328541 6:144370691 G 5325 NM_001080951.1 Transcript intron_variant - - - - - - rs2328541 6:144370691 G ENSESTG00000035139 ENSESTT00000088805 Transcript intron_variant - - - - - - rs2328541 6:144370691 G 5325 NM_001080955.1 Transcript intron_variant - - - - - - rs2328566 6:144565790 C - - - intergenic_variant - - - - - - rs4243471 6:144802806 T 7402 NM_007124.2 Transcript intron_variant - - - - - - rs4243471 6:144802806 T ENSESTG00000035094 ENSESTT00000088689 Transcript intron_variant - - - - - - rs4243471 6:144802806 T ENSESTG00000035094 ENSESTT00000088686 Transcript intron_variant - - - - - - rs4243471 6:144802806 T CCDS34547.1 CCDS34547.1 Transcript intron_variant - - - - - - rs6570638 6:144959718 A 7402 NM_007124.2 Transcript intron_variant - - - - - - rs6570638 6:144959718 A ENSESTG00000035114 ENSESTT00000088752 Transcript intron_variant - - - - - - rs6570638 6:144959718 A CCDS34547.1 CCDS34547.1 Transcript intron_variant - - - - - - rs6570638 6:144959718 A ENSESTG00000035114 ENSESTT00000088753 Transcript intron_variant - - - - - - rs6570638 6:144959718 A ENSESTG00000035114 ENSESTT00000088758 Transcript intron_variant - - - - - - rs6570638 6:144959718 A ENSESTG00000035114 ENSESTT00000088755 Transcript intron_variant - - - - - - rs7768900 6:145232662 C - - - intergenic_variant - - - - - - rs559621 6:145618444 T - - - intergenic_variant - - - - - - rs1155115 6:145779781 G - - - intergenic_variant - - - - - - rs3918991 6:145963467 A ENSESTG00000002770 ENSESTT00000006870 Transcript intron_variant - - - - - - rs3918991 6:145963467 A 7957 NM_005670.3 Transcript intron_variant - - - - - - rs3918991 6:145963467 A ENSESTG00000002770 ENSESTT00000006877 Transcript intron_variant - - - - - - rs3918991 6:145963467 A ENSESTG00000002770 ENSESTT00000006873 Transcript intron_variant - - - - - - rs3918991 6:145963467 A 7957 NM_001018041.1 Transcript intron_variant - - - - - - rs3918991 6:145963467 A CCDS5206.1 CCDS5206.1 Transcript intron_variant - - - - - - rs3918991 6:145963467 A ENSESTG00000002770 ENSESTT00000006865 Transcript intron_variant - - - - - - rs3918991 6:145963467 A ENSESTG00000002770 ENSESTT00000006868 Transcript intron_variant - - - - - - rs857876 6:145977515 C ENSESTG00000002770 ENSESTT00000006870 Transcript intron_variant - - - - - - rs857876 6:145977515 C 7957 NM_005670.3 Transcript intron_variant - - - - - - rs857876 6:145977515 C ENSESTG00000002770 ENSESTT00000006877 Transcript intron_variant - - - - - - rs857876 6:145977515 C ENSESTG00000002770 ENSESTT00000006873 Transcript intron_variant - - - - - - rs857876 6:145977515 C 7957 NM_001018041.1 Transcript intron_variant - - - - - - rs857876 6:145977515 C CCDS5206.1 CCDS5206.1 Transcript intron_variant - - - - - - rs857876 6:145977515 C ENSESTG00000002770 ENSESTT00000006865 Transcript intron_variant - - - - - - rs857876 6:145977515 C ENSESTG00000002770 ENSESTT00000006868 Transcript intron_variant - - - - - - rs6570733 6:146275302 G ENSESTG00000017152 ENSESTT00000043073 Transcript intron_variant - - - - - - rs6570733 6:146275302 G CCDS43513.2 CCDS43513.2 Transcript intron_variant - - - - - - rs6570733 6:146275302 G ENSESTG00000017152 ENSESTT00000043093 Transcript downstream_gene_variant - - - - - - DISTANCE=678 rs6570733 6:146275302 G CCDS47496.1 CCDS47496.1 Transcript intron_variant - - - - - - rs6570733 6:146275302 G ENSESTG00000017152 ENSESTT00000043080 Transcript intron_variant - - - - - - rs6570733 6:146275302 G 257218 NM_001042683.2 Transcript intron_variant - - - - - - rs6570733 6:146275302 G 257218 NM_173082.3 Transcript intron_variant - - - - - - rs1012772 6:146367071 A CCDS5209.1 CCDS5209.1 Transcript intron_variant - - - - - - rs1012772 6:146367071 A ENSESTG00000016996 ENSESTT00000042671 Transcript intron_variant - - - - - - rs1012772 6:146367071 A CCDS47497.1 CCDS47497.1 Transcript intron_variant - - - - - - rs1012772 6:146367071 A 2911 NM_000838.3 Transcript intron_variant - - - - - - rs1012772 6:146367071 A 2911 NM_001114329.1 Transcript intron_variant - - - - - - rs6937564 6:146483551 G CCDS5209.1 CCDS5209.1 Transcript intron_variant - - - - - - rs6937564 6:146483551 G ENSESTG00000016996 ENSESTT00000042671 Transcript intron_variant - - - - - - rs6937564 6:146483551 G CCDS47497.1 CCDS47497.1 Transcript intron_variant - - - - - - rs6937564 6:146483551 G 2911 NM_000838.3 Transcript intron_variant - - - - - - rs6937564 6:146483551 G 2911 NM_001114329.1 Transcript intron_variant - - - - - - rs4419686 6:146489191 A CCDS5209.1 CCDS5209.1 Transcript intron_variant - - - - - - rs4419686 6:146489191 A ENSESTG00000016996 ENSESTT00000042671 Transcript intron_variant - - - - - - rs4419686 6:146489191 A CCDS47497.1 CCDS47497.1 Transcript intron_variant - - - - - - rs4419686 6:146489191 A 2911 NM_000838.3 Transcript intron_variant - - - - - - rs4419686 6:146489191 A 2911 NM_001114329.1 Transcript intron_variant - - - - - - rs6931209 6:146715831 T CCDS5209.1 CCDS5209.1 Transcript intron_variant - - - - - - rs6931209 6:146715831 T ENSESTG00000017005 ENSESTT00000042707 Transcript upstream_gene_variant - - - - - - DISTANCE=4566 rs6931209 6:146715831 T CCDS47497.1 CCDS47497.1 Transcript intron_variant - - - - - - rs6931209 6:146715831 T ENSESTG00000017005 ENSESTT00000042684 Transcript upstream_gene_variant - - - - - - DISTANCE=4445 rs6931209 6:146715831 T 2911 NM_000838.3 Transcript intron_variant - - - - - - rs6931209 6:146715831 T 2911 NM_001114329.1 Transcript intron_variant - - - - - - rs2143743 6:146728917 T CCDS5209.1 CCDS5209.1 Transcript intron_variant - - - - - - rs2143743 6:146728917 T ENSESTG00000017005 ENSESTT00000042707 Transcript intron_variant - - - - - - rs2143743 6:146728917 T CCDS47497.1 CCDS47497.1 Transcript intron_variant - - - - - - rs2143743 6:146728917 T ENSESTG00000017005 ENSESTT00000042684 Transcript intron_variant - - - - - - rs2143743 6:146728917 T 2911 NM_000838.3 Transcript intron_variant - - - - - - rs2143743 6:146728917 T 2911 NM_001114329.1 Transcript intron_variant - - - - - - rs1590448 6:147247827 C 729178 NR_034115.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1590448 6:147247827 C ENSESTG00000017128 ENSESTT00000043034 Transcript intron_variant - - - - - - rs642288 6:147712636 T ENSESTG00000035143 ENSESTT00000088804 Transcript downstream_gene_variant - - - - - - DISTANCE=1841 rs642288 6:147712636 T 134957 NM_139244.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1024 rs642288 6:147712636 T 134957 NM_001127715.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1024 rs1231942 6:148135121 T - - - intergenic_variant - - - - - - rs62431648 6:148364488 T ENSESTG00000003985 ENSESTT00000010079 Transcript intron_variant - - - - - - rs1890965 6:148468274 A - ENSR00001230124 RegulatoryFeature regulatory_region_variant - - - - - - rs1890965 6:148468274 A - - - intergenic_variant - - - - - - rs1809473 6:149159202 C - ENSR00001230293 RegulatoryFeature regulatory_region_variant - - - - - - rs1809473 6:149159202 C ENSESTG00000003963 ENSESTT00000010050 Transcript intron_variant - - - - - - rs1809473 6:149159202 C CCDS5213.1 CCDS5213.1 Transcript intron_variant - - - - - - rs1809473 6:149159202 C 10090 NM_005715.2 Transcript intron_variant - - - - - - rs1809473 6:149159202 C ENSESTG00000003963 ENSESTT00000010049 Transcript intron_variant - - - - - - rs379916 6:149735350 C 23118 NM_015093.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2603 rs379916 6:149735350 C CCDS5214.1 CCDS5214.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4495 rs379916 6:149735350 C ENSESTG00000014980 ENSESTT00000037607 Transcript downstream_gene_variant - - - - - - DISTANCE=3816 rs1538497 6:149842629 A ENSESTG00000015296 ENSESTT00000038353 Transcript intron_variant - - - - - - rs1538497 6:149842629 A ENSESTG00000015274 ENSESTT00000038290 Transcript intron_variant - - - - - - rs1538497 6:149842629 A CCDS34550.1 CCDS34550.1 Transcript intron_variant - - - - - - rs1538497 6:149842629 A 85313 NM_139126.3 Transcript intron_variant - - - - - - rs674131 6:150709307 G CCDS55066.1 CCDS55066.1 Transcript intron_variant - - - - - - rs674131 6:150709307 G ENSESTG00000032279 ENSESTT00000081463 Transcript intron_variant - - - - - - rs674131 6:150709307 G 389434 NM_001164695.1 Transcript intron_variant - - - - - - rs674131 6:150709307 G CCDS55067.1 CCDS55067.1 Transcript intron_variant - - - - - - rs674131 6:150709307 G CCDS5227.1 CCDS5227.1 Transcript intron_variant - - - - - - rs674131 6:150709307 G 389434 NM_203395.2 Transcript intron_variant - - - - - - rs674131 6:150709307 G 389434 NM_001164694.1 Transcript intron_variant - - - - - - rs803423 6:151211699 A CCDS56457.1 CCDS56457.1 Transcript intron_variant - - - - - - rs803423 6:151211699 A CCDS5228.1 CCDS5228.1 Transcript intron_variant - - - - - - rs803423 6:151211699 A 25902 NM_001242768.1 Transcript intron_variant - - - - - - rs803423 6:151211699 A ENSESTG00000032339 ENSESTT00000081725 Transcript intron_variant - - - - - - rs803423 6:151211699 A 25902 NM_001242769.1 Transcript intron_variant - - - - - - rs803423 6:151211699 A 25902 NM_001242767.1 Transcript intron_variant - - - - - - rs803423 6:151211699 A 25902 NM_015440.4 Transcript intron_variant - - - - - - rs1293959 6:151986689 C - - - intergenic_variant - - - - - - rs1293958 6:151986735 T - - - intergenic_variant - - - - - - rs851979 6:152028040 C 2099 NM_001122742.1 Transcript intron_variant - - - - - - rs1285060 6:152119349 G 2099 NM_001122742.1 Transcript intron_variant - - - - - - rs651306 6:152550015 T CCDS5235.1 CCDS5235.1 Transcript intron_variant - - - - - - rs651306 6:152550015 T 23345 NM_182961.3 Transcript intron_variant - - - - - - rs651306 6:152550015 T CCDS5236.2 CCDS5236.2 Transcript intron_variant - - - - - - rs651306 6:152550015 T 23345 NM_033071.3 Transcript intron_variant - - - - - - rs651306 6:152550015 T ENSESTG00000027532 ENSESTT00000069331 Transcript intron_variant - - - - - - rs311350 6:153106726 G - - - intergenic_variant - - - - - - rs3860814 6:153311001 C 54516 NM_019041.5 Transcript 3_prime_UTR_variant 1277 - - - - - rs3860814 6:153311001 C ENSESTG00000016277 ENSESTT00000040895 Transcript downstream_gene_variant - - - - - - DISTANCE=1336 rs3860814 6:153311001 C CCDS47502.1 CCDS47502.1 Transcript downstream_gene_variant - - - - - - DISTANCE=219 rs3860814 6:153311001 C CCDS5243.1 CCDS5243.1 Transcript downstream_gene_variant - - - - - - DISTANCE=29 rs3860814 6:153311001 C 54516 NM_001114184.1 Transcript 3_prime_UTR_variant 1140 - - - - - rs3860814 6:153311001 C ENSESTG00000016203 ENSESTT00000040669 Transcript downstream_gene_variant - - - - - - DISTANCE=546 rs317103 6:153567055 C ENSESTG00000016212 ENSESTT00000040703 Transcript intron_variant - - - - - - rs2503793 6:153658481 G ENSESTG00000016212 ENSESTT00000040703 Transcript intron_variant - - - - - - rs9384197 6:154594802 A - ENSR00001231218 RegulatoryFeature regulatory_region_variant - - - - - - rs9384197 6:154594802 A 26034 NM_001130700.1 Transcript intron_variant - - - - - - rs9384197 6:154594802 A 26034 NM_015553.2 Transcript intron_variant - - - - - - rs9384197 6:154594802 A 26034 NM_001130699.1 Transcript intron_variant - - - - - - rs2056371 6:154919253 C - - - intergenic_variant - - - - - - rs909027 6:154992396 T - - - intergenic_variant - - - - - - rs6918349 6:155825898 A - - - intergenic_variant - - - - - - rs2817436 6:156924147 T - - - intergenic_variant - - - - - - rs4242302 6:156967496 T - - - intergenic_variant - - - - - - rs9480422 6:157363075 G 57492 NM_017519.2 Transcript intron_variant - - - - - - rs9480422 6:157363075 G ENSESTG00000017353 ENSESTT00000043629 Transcript intron_variant - - - - - - rs9480422 6:157363075 G ENSESTG00000014492 ENSESTT00000036309 Transcript intron_variant - - - - - - rs9480422 6:157363075 G CCDS55072.1 CCDS55072.1 Transcript intron_variant - - - - - - rs9480422 6:157363075 G CCDS5251.2 CCDS5251.2 Transcript intron_variant - - - - - - rs9480422 6:157363075 G 57492 NM_020732.3 Transcript intron_variant - - - - - - rs1547603 6:157371306 C 57492 NM_017519.2 Transcript intron_variant - - - - - - rs1547603 6:157371306 C ENSESTG00000017353 ENSESTT00000043629 Transcript intron_variant - - - - - - rs1547603 6:157371306 C ENSESTG00000014492 ENSESTT00000036309 Transcript intron_variant - - - - - - rs1547603 6:157371306 C CCDS55072.1 CCDS55072.1 Transcript intron_variant - - - - - - rs1547603 6:157371306 C CCDS5251.2 CCDS5251.2 Transcript intron_variant - - - - - - rs1547603 6:157371306 C 57492 NM_020732.3 Transcript intron_variant - - - - - - rs13211034 6:157692950 G - - - intergenic_variant - - - - - - rs62422795 6:157777888 T - - - intergenic_variant - - - - - - rs2770106 6:158235003 A - ENSR00001501978 RegulatoryFeature regulatory_region_variant - - - - - - rs2770106 6:158235003 A ENSESTG00000017471 ENSESTT00000043945 Transcript intron_variant - - - - - - rs2770106 6:158235003 A ENSESTG00000017471 ENSESTT00000043965 Transcript intron_variant - - - - - - rs9347225 6:158726607 T ENSESTG00000015610 ENSESTT00000039100 Transcript intron_variant - - - - - - rs9347225 6:158726607 T ENSESTG00000015610 ENSESTT00000039103 Transcript intron_variant - - - - - - rs827955 6:158855953 A ENSESTG00000015783 ENSESTT00000039522 Transcript intron_variant - - - - - - rs827955 6:158855953 A CCDS34561.1 CCDS34561.1 Transcript intron_variant - - - - - - rs827955 6:158855953 A 56995 NM_020245.4 Transcript intron_variant - - - - - - rs827955 6:158855953 A 56995 NM_001007466.2 Transcript intron_variant - - - - - - rs827955 6:158855953 A CCDS34562.1 CCDS34562.1 Transcript intron_variant - - - - - - rs2341529 6:159822586 C ENSESTG00000031486 ENSESTT00000079428 Transcript intron_variant - - - - - - rs240869 6:159991945 A - - - intergenic_variant - - - - - - rs911845 6:160198748 C CCDS43522.1 CCDS43522.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1329 rs911845 6:160198748 C ENSESTG00000031952 ENSESTT00000080651 Transcript intron_variant - - - - - - rs911845 6:160198748 C 677806 NR_002960.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2534 rs911845 6:160198748 C 6950 NM_001008897.1 Transcript downstream_gene_variant - - - - - - DISTANCE=782 rs911845 6:160198748 C ENSESTG00000032922 ENSESTT00000083366 Transcript downstream_gene_variant - - - - - - DISTANCE=1236 rs911845 6:160198748 C CCDS5268.1 CCDS5268.1 Transcript intron_variant - - - - - - rs911845 6:160198748 C ENSESTG00000031927 ENSESTT00000080608 Transcript downstream_gene_variant - - - - - - DISTANCE=1443 rs911845 6:160198748 C ENSESTG00000031927 ENSESTT00000080590 Transcript downstream_gene_variant - - - - - - DISTANCE=1443 rs911845 6:160198748 C CCDS5269.1 CCDS5269.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1329 rs911845 6:160198748 C 6950 NM_030752.2 Transcript downstream_gene_variant - - - - - - DISTANCE=782 rs911845 6:160198748 C 39 NM_005891.2 Transcript intron_variant - - - - - - rs6905994 6:160220272 A CCDS5271.1 CCDS5271.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1489 rs6905994 6:160220272 A ENSESTG00000032000 ENSESTT00000080790 Transcript upstream_gene_variant - - - - - - DISTANCE=1034 rs6905994 6:160220272 A 29074 NM_014161.3 Transcript downstream_gene_variant - - - - - - DISTANCE=811 rs6905994 6:160220272 A ENSESTG00000032000 ENSESTT00000080758 Transcript upstream_gene_variant - - - - - - DISTANCE=1029 rs6905994 6:160220272 A ENSESTG00000031965 ENSESTT00000080676 Transcript downstream_gene_variant - - - - - - DISTANCE=1046 rs6905994 6:160220272 A CCDS5270.1 CCDS5270.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1117 rs6905994 6:160220272 A ENSESTG00000032000 ENSESTT00000080771 Transcript upstream_gene_variant - - - - - - DISTANCE=1031 rs6905994 6:160220272 A ENSESTG00000032000 ENSESTT00000080779 Transcript upstream_gene_variant - - - - - - DISTANCE=1034 rs6905994 6:160220272 A 154197 NM_173516.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1029 rs6905994 6:160220272 A ENSESTG00000032000 ENSESTT00000080799 Transcript upstream_gene_variant - - - - - - DISTANCE=1039 rs6905994 6:160220272 A ENSESTG00000031965 ENSESTT00000080734 Transcript downstream_gene_variant - - - - - - DISTANCE=812 rs620571 6:160733560 C - - - intergenic_variant - - - - - - rs371633 6:160747283 C - - - intergenic_variant - - - - - - rs6455694 6:161027330 C CCDS43523.1 CCDS43523.1 Transcript intron_variant - - - - - - rs6455694 6:161027330 C 4018 NM_005577.2 Transcript intron_variant - - - - - - rs2586974 6:161422895 T ENSESTG00000031256 ENSESTT00000079065 Transcript intron_variant - - - - - - rs2586974 6:161422895 T ENSESTG00000031256 ENSESTT00000079008 Transcript intron_variant - - - - - - rs2586974 6:161422895 T ENSESTG00000031256 ENSESTT00000079031 Transcript intron_variant - - - - - - rs2586974 6:161422895 T CCDS34566.1 CCDS34566.1 Transcript intron_variant - - - - - - rs2586974 6:161422895 T 4216 NM_006724.2 Transcript intron_variant - - - - - - rs2586974 6:161422895 T 4216 NM_005922.2 Transcript intron_variant - - - - - - rs2586974 6:161422895 T ENSESTG00000031256 ENSESTT00000078967 Transcript intron_variant - - - - - - rs2586974 6:161422895 T ENSESTG00000031256 ENSESTT00000079026 Transcript intron_variant - - - - - - rs2586974 6:161422895 T CCDS34565.1 CCDS34565.1 Transcript intron_variant - - - - - - rs2586974 6:161422895 T ENSESTG00000031256 ENSESTT00000079022 Transcript intron_variant - - - - - - rs453493 6:161677681 C ENSESTG00000031582 ENSESTT00000079720 Transcript intron_variant - - - - - - rs453493 6:161677681 C ENSESTG00000031582 ENSESTT00000079732 Transcript intron_variant - - - - - - rs453493 6:161677681 C 56895 NM_020133.2 Transcript intron_variant - - - - - - rs4286750 6:162063879 T 5071 NM_013987.2 Transcript intron_variant - - - - - - rs4286750 6:162063879 T CCDS5283.1 CCDS5283.1 Transcript intron_variant - - - - - - rs4286750 6:162063879 T CCDS5281.1 CCDS5281.1 Transcript intron_variant - - - - - - rs4286750 6:162063879 T CCDS5282.1 CCDS5282.1 Transcript intron_variant - - - - - - rs4286750 6:162063879 T 5071 NM_004562.2 Transcript intron_variant - - - - - - rs4286750 6:162063879 T 5071 NM_013988.2 Transcript intron_variant - - - - - - rs9295160 6:162106644 G 5071 NM_013987.2 Transcript intron_variant - - - - - - rs9295160 6:162106644 G CCDS5283.1 CCDS5283.1 Transcript intron_variant - - - - - - rs9295160 6:162106644 G CCDS5281.1 CCDS5281.1 Transcript intron_variant - - - - - - rs9295160 6:162106644 G CCDS5282.1 CCDS5282.1 Transcript intron_variant - - - - - - rs9295160 6:162106644 G 5071 NM_004562.2 Transcript intron_variant - - - - - - rs9295160 6:162106644 G 5071 NM_013988.2 Transcript intron_variant - - - - - - rs3019423 6:162129868 A 5071 NM_013987.2 Transcript intron_variant - - - - - - rs3019423 6:162129868 A CCDS5283.1 CCDS5283.1 Transcript intron_variant - - - - - - rs3019423 6:162129868 A CCDS5281.1 CCDS5281.1 Transcript intron_variant - - - - - - rs3019423 6:162129868 A CCDS5282.1 CCDS5282.1 Transcript intron_variant - - - - - - rs3019423 6:162129868 A 5071 NM_004562.2 Transcript intron_variant - - - - - - rs3019423 6:162129868 A 5071 NM_013988.2 Transcript intron_variant - - - - - - rs3019422 6:162129947 A 5071 NM_013987.2 Transcript intron_variant - - - - - - rs3019422 6:162129947 A CCDS5283.1 CCDS5283.1 Transcript intron_variant - - - - - - rs3019422 6:162129947 A CCDS5281.1 CCDS5281.1 Transcript intron_variant - - - - - - rs3019422 6:162129947 A CCDS5282.1 CCDS5282.1 Transcript intron_variant - - - - - - rs3019422 6:162129947 A 5071 NM_004562.2 Transcript intron_variant - - - - - - rs3019422 6:162129947 A 5071 NM_013988.2 Transcript intron_variant - - - - - - rs1893546 6:162584701 T CCDS5282.1 CCDS5282.1 Transcript intron_variant - - - - - - rs1893546 6:162584701 T ENSESTG00000018691 ENSESTT00000047437 Transcript intron_variant - - - - - - rs1893546 6:162584701 T ENSESTG00000018691 ENSESTT00000047386 Transcript intron_variant - - - - - - rs1893546 6:162584701 T 5071 NM_013988.2 Transcript intron_variant - - - - - - rs1893546 6:162584701 T 5071 NM_013987.2 Transcript intron_variant - - - - - - rs1893546 6:162584701 T CCDS5283.1 CCDS5283.1 Transcript intron_variant - - - - - - rs1893546 6:162584701 T CCDS5281.1 CCDS5281.1 Transcript intron_variant - - - - - - rs1893546 6:162584701 T 5071 NM_004562.2 Transcript intron_variant - - - - - - rs1893546 6:162584701 T ENSESTG00000018691 ENSESTT00000047379 Transcript intron_variant - - - - - - rs2023088 6:162754693 T ENSESTG00000018691 ENSESTT00000047428 Transcript intron_variant - - - - - - rs2023088 6:162754693 T CCDS5282.1 CCDS5282.1 Transcript intron_variant - - - - - - rs2023088 6:162754693 T ENSESTG00000018691 ENSESTT00000047386 Transcript intron_variant - - - - - - rs2023088 6:162754693 T 5071 NM_013988.2 Transcript intron_variant - - - - - - rs2023088 6:162754693 T 5071 NM_013987.2 Transcript intron_variant - - - - - - rs2023088 6:162754693 T CCDS5283.1 CCDS5283.1 Transcript intron_variant - - - - - - rs2023088 6:162754693 T CCDS5281.1 CCDS5281.1 Transcript intron_variant - - - - - - rs2023088 6:162754693 T 5071 NM_004562.2 Transcript intron_variant - - - - - - rs2023088 6:162754693 T ENSESTG00000018691 ENSESTT00000047379 Transcript intron_variant - - - - - - rs2155498 6:162889291 G 5071 NM_013987.2 Transcript intron_variant - - - - - - rs2155498 6:162889291 G CCDS5283.1 CCDS5283.1 Transcript intron_variant - - - - - - rs2155498 6:162889291 G CCDS5281.1 CCDS5281.1 Transcript intron_variant - - - - - - rs2155498 6:162889291 G CCDS5282.1 CCDS5282.1 Transcript intron_variant - - - - - - rs2155498 6:162889291 G 5071 NM_004562.2 Transcript intron_variant - - - - - - rs2155498 6:162889291 G 5071 NM_013988.2 Transcript intron_variant - - - - - - rs9295199 6:163244313 T CCDS5284.1 CCDS5284.1 Transcript intron_variant - - - - - - rs9295199 6:163244313 T CCDS43524.1 CCDS43524.1 Transcript intron_variant - - - - - - rs9295199 6:163244313 T 135138 NM_001080379.1 Transcript intron_variant - - - - - - rs9295199 6:163244313 T 135138 NM_152410.2 Transcript intron_variant - - - - - - rs9295199 6:163244313 T 135138 NM_001080378.1 Transcript intron_variant - - - - - - rs1040515 6:163927473 G ENSESTG00000032168 ENSESTT00000081164 Transcript intron_variant - - - - - - rs1040515 6:163927473 G CCDS5285.1 CCDS5285.1 Transcript intron_variant - - - - - - rs1040515 6:163927473 G CCDS5287.1 CCDS5287.1 Transcript intron_variant - - - - - - rs1040515 6:163927473 G ENSESTG00000032108 ENSESTT00000081097 Transcript intron_variant - - - - - - rs1040515 6:163927473 G CCDS43525.1 CCDS43525.1 Transcript intron_variant - - - - - - rs1040515 6:163927473 G CCDS5286.1 CCDS5286.1 Transcript intron_variant - - - - - - rs1040515 6:163927473 G 9444 NM_206855.2 Transcript intron_variant - - - - - - rs1040515 6:163927473 G 9444 NM_206853.2 Transcript intron_variant - - - - - - rs1040515 6:163927473 G 9444 NM_206854.2 Transcript intron_variant - - - - - - rs1040515 6:163927473 G ENSESTG00000032108 ENSESTT00000081066 Transcript intron_variant - - - - - - rs1040515 6:163927473 G ENSESTG00000032108 ENSESTT00000081083 Transcript intron_variant - - - - - - rs1040515 6:163927473 G 9444 NM_006775.2 Transcript intron_variant - - - - - - rs1040515 6:163927473 G ENSESTG00000032108 ENSESTT00000081090 Transcript intron_variant - - - - - - rs2322374 6:164883139 A - - - intergenic_variant - - - - - - rs495231 6:165951167 C ENSESTG00000006721 ENSESTT00000017033 Transcript intron_variant - - - - - - rs495231 6:165951167 C CCDS47513.1 CCDS47513.1 Transcript intron_variant - - - - - - rs495231 6:165951167 C ENSESTG00000006721 ENSESTT00000017036 Transcript intron_variant - - - - - - rs495231 6:165951167 C 10846 NM_001130690.2 Transcript intron_variant - - - - - - rs495231 6:165951167 C 10846 NR_045597.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6456003 6:166075362 T - ENSR00001233153 RegulatoryFeature regulatory_region_variant - - - - - - rs6456003 6:166075362 T ENSESTG00000006721 ENSESTT00000017033 Transcript intron_variant - - - - - - rs6456003 6:166075362 T CCDS47513.1 CCDS47513.1 Transcript intron_variant - - - - - - rs6456003 6:166075362 T 10846 NM_001130690.2 Transcript intron_variant - - - - - - rs6456003 6:166075362 T 10846 NR_045597.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7740126 6:166261751 G - ENSR00001502580 RegulatoryFeature regulatory_region_variant - - - - - - rs7740126 6:166261751 G - - - intergenic_variant - - - - - - rs3099343 6:166493162 G - - - intergenic_variant - - - - - - rs9356572 6:167639232 C - ENSR00001233525 RegulatoryFeature regulatory_region_variant - - - - - - rs9356572 6:167639232 C - - - intergenic_variant - - - - - - rs642533 6:168353643 A ENSESTG00000030285 ENSESTT00000076576 Transcript intron_variant - - - - - - rs642533 6:168353643 A CCDS47517.1 CCDS47517.1 Transcript intron_variant - - - - - - rs642533 6:168353643 A ENSESTG00000030285 ENSESTT00000076540 Transcript intron_variant - - - - - - rs642533 6:168353643 A ENSESTG00000030285 ENSESTT00000076570 Transcript intron_variant - - - - - - rs642533 6:168353643 A 4301 NM_001207008.1 Transcript intron_variant - - - - - - rs642533 6:168353643 A ENSESTG00000030285 ENSESTT00000076574 Transcript intron_variant - - - - - - rs642533 6:168353643 A ENSESTG00000030285 ENSESTT00000076493 Transcript intron_variant - - - - - - rs642533 6:168353643 A ENSESTG00000030285 ENSESTT00000076546 Transcript intron_variant - - - - - - rs642533 6:168353643 A 4301 NM_001040000.2 Transcript intron_variant - - - - - - rs642533 6:168353643 A ENSESTG00000030285 ENSESTT00000076476 Transcript intron_variant - - - - - - rs642533 6:168353643 A ENSESTG00000030285 ENSESTT00000076561 Transcript intron_variant - - - - - - rs4708685 6:168592957 C ENSESTG00000017539 ENSESTT00000044111 Transcript upstream_gene_variant - - - - - - DISTANCE=2089 rs4147363 6:168629594 G ENSESTG00000017684 ENSESTT00000044553 Transcript upstream_gene_variant - - - - - - DISTANCE=2397 rs12527570 6:168647003 G ENSESTG00000017541 ENSESTT00000044122 Transcript intron_variant - - - - - - rs12527570 6:168647003 G ENSESTG00000017541 ENSESTT00000044118 Transcript intron_variant - - - - - - rs4708704 6:168648671 G ENSESTG00000017541 ENSESTT00000044122 Transcript intron_variant - - - - - - rs4708704 6:168648671 G ENSESTG00000017541 ENSESTT00000044118 Transcript intron_variant - - - - - - rs7748050 6:168721776 T ENSESTG00000017658 ENSESTT00000044499 Transcript upstream_gene_variant - - - - - - DISTANCE=1338 rs7748050 6:168721776 T CCDS47519.1 CCDS47519.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1463 rs7748050 6:168721776 T 168002 NM_214462.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1374 rs4235918 6:168744506 G - - - intergenic_variant - - - - - - rs6941821 6:168757255 A - - - intergenic_variant - - - - - - rs994838 6:169544389 G - - - intergenic_variant - - - - - - rs4236174 6:170047435 C CCDS47520.2 CCDS47520.2 Transcript intron_variant - - - - - - rs4236174 6:170047435 C ENSESTG00000025345 ENSESTT00000064113 Transcript intron_variant - - - - - - rs4236174 6:170047435 C ENSESTG00000025345 ENSESTT00000064086 Transcript downstream_gene_variant - - - - - - DISTANCE=316 rs4236174 6:170047435 C 253769 NM_001202550.1 Transcript intron_variant - - - - - - rs4236174 6:170047435 C 253769 NM_182552.4 Transcript intron_variant - - - - - - rs4236174 6:170047435 C CCDS56459.1 CCDS56459.1 Transcript intron_variant - - - - - - rs4236174 6:170047435 C ENSESTG00000025345 ENSESTT00000064134 Transcript intron_variant - - - - - - rs7760142 6:170118085 T ENSESTG00000025257 ENSESTT00000063898 Transcript intron_variant - - - - - - rs7760142 6:170118085 T CCDS5309.2 CCDS5309.2 Transcript intron_variant - - - - - - rs7760142 6:170118085 T ENSESTG00000025257 ENSESTT00000063891 Transcript intron_variant - - - - - - rs7760142 6:170118085 T CCDS5308.2 CCDS5308.2 Transcript intron_variant - - - - - - rs7760142 6:170118085 T 55274 NM_018288.3 Transcript intron_variant - - - - - - rs7760142 6:170118085 T ENSESTG00000025257 ENSESTT00000063877 Transcript intron_variant - - - - - - rs7760142 6:170118085 T 55274 NM_133325.2 Transcript intron_variant - - - - - - rs2092310 6:170895529 G 5134 NM_001199461.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1749 rs2092310 6:170895529 G CCDS47521.1 CCDS47521.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1860 rs2092310 6:170895529 G CCDS56462.1 CCDS56462.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1860 rs2092310 6:170895529 G CCDS5316.1 CCDS5316.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1860 rs2092310 6:170895529 G CCDS56461.1 CCDS56461.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1860 rs2092310 6:170895529 G 5134 NM_001199463.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1787 rs2092310 6:170895529 G CCDS56460.1 CCDS56460.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1860 rs2092310 6:170895529 G 5134 NM_001199464.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1787 rs2092310 6:170895529 G 5134 NM_144781.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1749 rs2092310 6:170895529 G 5134 NM_002598.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1749 rs2092310 6:170895529 G 5134 NM_001199462.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1787 rs4283996 7:124465 G - ENSR00000681397 RegulatoryFeature regulatory_region_variant - - - - - - rs4283996 7:124465 G - - - intergenic_variant - - - - - - rs11185561 7:190156 T CCDS47522.1 CCDS47522.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3044 rs11185561 7:190156 T 56975 NM_020223.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2813 rs11185561 7:190156 T ENSESTG00000017734 ENSESTT00000044693 Transcript upstream_gene_variant - - - - - - DISTANCE=2426 rs11185561 7:190156 T ENSESTG00000017734 ENSESTT00000044699 Transcript upstream_gene_variant - - - - - - DISTANCE=2426 rs11185561 7:190156 T ENSESTG00000017734 ENSESTT00000044709 Transcript upstream_gene_variant - - - - - - DISTANCE=2875 rs140952328 7:504813 C - ENSR00000620453 RegulatoryFeature regulatory_region_variant - - - - - - rs140952328 7:504813 C - - - intergenic_variant - - - - - - rs4722203 7:926827 C ENSESTG00000018124 ENSESTT00000045734 Transcript synonymous_variant 158 132 44 H caT/caC - rs4722203 7:926827 C ENSESTG00000018124 ENSESTT00000045811 Transcript upstream_gene_variant - - - - - - DISTANCE=1864 rs4722203 7:926827 C ENSESTG00000018124 ENSESTT00000045706 Transcript intron_variant - - - - - - rs4722203 7:926827 C CCDS5317.1 CCDS5317.1 Transcript intron_variant - - - - - - rs4722203 7:926827 C ENSESTG00000018203 ENSESTT00000045834 Transcript upstream_gene_variant - - - - - - DISTANCE=2749 rs4722203 7:926827 C ENSESTG00000018124 ENSESTT00000045725 Transcript downstream_gene_variant - - - - - - DISTANCE=597 rs4722203 7:926827 C ENSESTG00000018124 ENSESTT00000045731 Transcript intron_variant - - - - - - rs4722203 7:926827 C ENSESTG00000018124 ENSESTT00000045797 Transcript upstream_gene_variant - - - - - - DISTANCE=1864 rs4722203 7:926827 C 51608 NM_015949.2 Transcript intron_variant - - - - - - rs10273306 7:1583973 C - ENSR00000620779 RegulatoryFeature regulatory_region_variant - - - - - - rs10273306 7:1583973 C ENSESTG00000029221 ENSESTT00000073696 Transcript downstream_gene_variant - - - - - - DISTANCE=4058 rs10273306 7:1583973 C ENSESTG00000029694 ENSESTT00000074684 Transcript intron_variant - - - - - - rs10273306 7:1583973 C ENSESTG00000029221 ENSESTT00000073653 Transcript downstream_gene_variant - - - - - - DISTANCE=4132 rs10273306 7:1583973 C 202915 NM_001097620.1 Transcript 3_prime_UTR_variant 4174 - - - - - rs10273306 7:1583973 C CCDS5325.1 CCDS5325.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3962 rs10273306 7:1583973 C 7975 NM_002360.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1294 rs10273306 7:1583973 C ENSESTG00000029221 ENSESTT00000073642 Transcript downstream_gene_variant - - - - - - DISTANCE=3953 rs10273306 7:1583973 C ENSESTG00000029272 ENSESTT00000073722 Transcript upstream_gene_variant - - - - - - DISTANCE=1377 rs10273306 7:1583973 C CCDS43537.1 CCDS43537.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2615 rs10278645 7:1901646 C ENSESTG00000029545 ENSESTT00000074334 Transcript intron_variant - - - - - - rs10278645 7:1901646 C 8379 NM_001013836.1 Transcript intron_variant - - - - - - rs10278645 7:1901646 C ENSESTG00000029545 ENSESTT00000074349 Transcript intron_variant - - - - - - rs10278645 7:1901646 C 8379 NM_001013837.1 Transcript intron_variant - - - - - - rs10278645 7:1901646 C 8379 NM_003550.2 Transcript intron_variant - - - - - - rs10278645 7:1901646 C CCDS43539.1 CCDS43539.1 Transcript intron_variant - - - - - - rs10278645 7:1901646 C ENSESTG00000029545 ENSESTT00000074363 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000060979 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000060944 Transcript intron_variant - - - - - - rs1637734 7:2252019 G 8379 NM_001013836.1 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000061022 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000061012 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000060965 Transcript intron_variant - - - - - - rs1637734 7:2252019 G CCDS43539.1 CCDS43539.1 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000060925 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000060959 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000061041 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000061017 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000024059 ENSESTT00000060871 Transcript intron_variant - - - - - - rs1637734 7:2252019 G 8379 NM_003550.2 Transcript intron_variant - - - - - - rs1637734 7:2252019 G 8379 NM_001013837.1 Transcript intron_variant - - - - - - rs1637734 7:2252019 G ENSESTG00000029367 ENSESTT00000074012 Transcript intron_variant - - - - - - rs13307943 7:3023679 C ENSESTG00000021488 ENSESTT00000053926 Transcript intron_variant - - - - - - rs13307943 7:3023679 C ENSESTG00000021488 ENSESTT00000053911 Transcript intron_variant - - - - - - rs13307943 7:3023679 C 84433 NM_032415.4 Transcript intron_variant - - - - - - rs13307943 7:3023679 C ENSESTG00000021488 ENSESTT00000053903 Transcript intron_variant - - - - - - rs6462047 7:3416828 C CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs6462047 7:3416828 C 221935 NM_152744.3 Transcript intron_variant - - - - - - rs4722743 7:3420083 T CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs4722743 7:3420083 T 221935 NM_152744.3 Transcript intron_variant - - - - - - rs6977934 7:3507402 A CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs6977934 7:3507402 A 221935 NM_152744.3 Transcript intron_variant - - - - - - rs2705605 7:3635987 G CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs2705605 7:3635987 G 221935 NM_152744.3 Transcript intron_variant - - - - - - rs9639629 7:3774581 C ENSESTG00000021417 ENSESTT00000053764 Transcript intron_variant - - - - - - rs9639629 7:3774581 C ENSESTG00000021417 ENSESTT00000053716 Transcript intron_variant - - - - - - rs9639629 7:3774581 C ENSESTG00000021417 ENSESTT00000053745 Transcript intron_variant - - - - - - rs9639629 7:3774581 C CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs9639629 7:3774581 C ENSESTG00000021417 ENSESTT00000053735 Transcript intron_variant - - - - - - rs9639629 7:3774581 C 221935 NM_152744.3 Transcript intron_variant - - - - - - rs442624 7:3960510 G ENSESTG00000021417 ENSESTT00000053764 Transcript intron_variant - - - - - - rs442624 7:3960510 G ENSESTG00000021417 ENSESTT00000053745 Transcript intron_variant - - - - - - rs442624 7:3960510 G CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs442624 7:3960510 G 221935 NM_152744.3 Transcript intron_variant - - - - - - rs894778 7:4029840 G CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs894778 7:4029840 G 221935 NM_152744.3 Transcript intron_variant - - - - - - rs668160 7:4208220 C 221935 NM_001079653.1 Transcript intron_variant - - - - - - rs668160 7:4208220 C ENSESTG00000003391 ENSESTT00000008481 Transcript intron_variant - - - - - - rs668160 7:4208220 C CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs668160 7:4208220 C 221935 NM_152744.3 Transcript intron_variant - - - - - - rs597049 7:4208226 C 221935 NM_001079653.1 Transcript intron_variant - - - - - - rs597049 7:4208226 C ENSESTG00000003391 ENSESTT00000008481 Transcript intron_variant - - - - - - rs597049 7:4208226 C CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs597049 7:4208226 C 221935 NM_152744.3 Transcript intron_variant - - - - - - rs593851 7:4287148 C ENSESTG00000003408 ENSESTT00000008524 Transcript intron_variant - - - - - - rs593851 7:4287148 C 221935 NM_001079653.1 Transcript intron_variant - - - - - - rs593851 7:4287148 C CCDS34590.1 CCDS34590.1 Transcript intron_variant - - - - - - rs593851 7:4287148 C ENSESTG00000003408 ENSESTT00000008531 Transcript intron_variant - - - - - - rs593851 7:4287148 C 221935 NM_152744.3 Transcript intron_variant - - - - - - rs314656 7:4440664 G - - - intergenic_variant - - - - - - rs2343562 7:4644989 C - - - intergenic_variant - - - - - - rs4723930 7:4649308 C - - - intergenic_variant - - - - - - rs7800801 7:5058923 C - - - intergenic_variant - - - - - - rs6463245 7:5114343 G CCDS56463.1 CCDS56463.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2247 rs6463245 7:5114343 G 100533952 NM_001204513.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1489 rs6463245 7:5114343 G ENSESTG00000035543 ENSESTT00000089784 Transcript downstream_gene_variant - - - - - - DISTANCE=1492 rs6463245 7:5114343 G ENSESTG00000035543 ENSESTT00000089781 Transcript downstream_gene_variant - - - - - - DISTANCE=1492 rs6463245 7:5114343 G ENSESTG00000035543 ENSESTT00000089772 Transcript downstream_gene_variant - - - - - - DISTANCE=1492 rs6463245 7:5114343 G ENSESTG00000035543 ENSESTT00000089780 Transcript downstream_gene_variant - - - - - - DISTANCE=1492 rs6463245 7:5114343 G 389458 NR_015343.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1489 rs4724717 7:5781860 T 54476 NM_207116.2 Transcript intron_variant - - - - - - rs4724717 7:5781860 T ENSESTG00000035617 ENSESTT00000089969 Transcript intron_variant - - - - - - rs4724717 7:5781860 T ENSESTG00000035617 ENSESTT00000089968 Transcript intron_variant - - - - - - rs4724717 7:5781860 T ENSESTG00000035617 ENSESTT00000089973 Transcript upstream_gene_variant - - - - - - DISTANCE=2739 rs4724717 7:5781860 T 54476 NM_207111.3 Transcript intron_variant - - - - - - rs4724717 7:5781860 T ENSESTG00000035617 ENSESTT00000089972 Transcript upstream_gene_variant - - - - - - DISTANCE=2737 rs4724717 7:5781860 T ENSESTG00000035617 ENSESTT00000089970 Transcript intron_variant - - - - - - rs4724717 7:5781860 T CCDS34595.1 CCDS34595.1 Transcript intron_variant - - - - - - rs4724717 7:5781860 T ENSESTG00000035617 ENSESTT00000089971 Transcript intron_variant - - - - - - rs4724717 7:5781860 T CCDS34594.1 CCDS34594.1 Transcript intron_variant - - - - - - rs11767538 7:6568804 G 392862 NM_001145118.1 Transcript intron_variant - - - - - - rs11767538 7:6568804 G CCDS47537.1 CCDS47537.1 Transcript intron_variant - - - - - - rs9784958 7:7833230 A - ENSR00000621741 RegulatoryFeature regulatory_region_variant - - - - - - rs9784958 7:7833230 A ENSESTG00000026563 ENSESTT00000067005 Transcript intron_variant - - - - - - rs9784958 7:7833230 A ENSESTG00000026563 ENSESTT00000066978 Transcript intron_variant - - - - - - rs9784958 7:7833230 A ENSESTG00000026563 ENSESTT00000067023 Transcript intron_variant - - - - - - rs9784958 7:7833230 A ENSESTG00000026563 ENSESTT00000066956 Transcript intron_variant - - - - - - rs9784958 7:7833230 A ENSESTG00000026563 ENSESTT00000066919 Transcript intron_variant - - - - - - rs9784958 7:7833230 A 729852 NR_034084.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9784958 7:7833230 A ENSESTG00000026563 ENSESTT00000066971 Transcript intron_variant - - - - - - rs2057863 7:8516224 T ENSESTG00000002051 ENSESTT00000005090 Transcript intron_variant - - - - - - rs2057863 7:8516224 T CCDS47540.1 CCDS47540.1 Transcript intron_variant - - - - - - rs2057863 7:8516224 T 30010 NM_152745.2 Transcript intron_variant - - - - - - rs988027 7:8537801 C ENSESTG00000002051 ENSESTT00000005090 Transcript intron_variant - - - - - - rs988027 7:8537801 C CCDS47540.1 CCDS47540.1 Transcript intron_variant - - - - - - rs988027 7:8537801 C 30010 NM_152745.2 Transcript intron_variant - - - - - - rs7795153 7:8927534 G - - - intergenic_variant - - - - - - rs10237570 7:8965782 G - - - intergenic_variant - - - - - - rs77933563 7:9061113 T - - - intergenic_variant - - - - - - rs12668494 7:9347221 T - - - intergenic_variant - - - - - - rs2915155 7:9956111 T - - - intergenic_variant - - - - - - rs10447580 7:10111766 A - - - intergenic_variant - - - - - - rs6960228 7:10123169 T - - - intergenic_variant - - - - - - rs222317 7:10226796 G - - - intergenic_variant - - - - - - rs4720873 7:10276438 G - - - intergenic_variant - - - - - - rs6960316 7:10359125 A - - - intergenic_variant - - - - - - rs4236423 7:10506765 G ENSESTG00000018740 ENSESTT00000047217 Transcript intron_variant - - - - - - rs4236423 7:10506765 G ENSESTG00000018740 ENSESTT00000047289 Transcript intron_variant - - - - - - rs6960505 7:10787395 C - - - intergenic_variant - - - - - - rs10250744 7:11155666 G ENSESTG00000011029 ENSESTT00000027667 Transcript intron_variant - - - - - - rs10250744 7:11155666 G 9678 NR_033436.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1029734 7:13187200 G - - - intergenic_variant - - - - - - rs7802614 7:13209893 T - - - intergenic_variant - - - - - - rs1029733 7:13221870 C - - - intergenic_variant - - - - - - rs194026 7:13235224 C - - - intergenic_variant - - - - - - rs10807763 7:13328146 T - - - intergenic_variant - - - - - - rs2160023 7:13351518 G - - - intergenic_variant - - - - - - rs252008 7:13893245 C ENSESTG00000000824 ENSESTT00000001993 Transcript downstream_gene_variant - - - - - - DISTANCE=736 rs4721299 7:14106982 C - - - intergenic_variant - - - - - - rs6958751 7:14110918 C - - - intergenic_variant - - - - - - rs1431537 7:14565623 G 1607 NM_145695.2 Transcript intron_variant - - - - - - rs1431537 7:14565623 G ENSESTG00000023786 ENSESTT00000060046 Transcript intron_variant - - - - - - rs1431537 7:14565623 G ENSESTG00000023786 ENSESTT00000060125 Transcript intron_variant - - - - - - rs1431537 7:14565623 G CCDS47548.1 CCDS47548.1 Transcript intron_variant - - - - - - rs1431537 7:14565623 G ENSESTG00000023786 ENSESTT00000060110 Transcript intron_variant - - - - - - rs1431537 7:14565623 G 1607 NM_004080.2 Transcript intron_variant - - - - - - rs1431537 7:14565623 G ENSESTG00000023786 ENSESTT00000060188 Transcript intron_variant - - - - - - rs1431537 7:14565623 G CCDS47547.1 CCDS47547.1 Transcript intron_variant - - - - - - rs217545 7:14898590 T - ENSR00001049192 RegulatoryFeature regulatory_region_variant - - - - - - rs217545 7:14898590 T ENSESTG00000023786 ENSESTT00000060076 Transcript intron_variant - - - - - - rs217545 7:14898590 T ENSESTG00000023786 ENSESTT00000060046 Transcript intron_variant - - - - - - rs217545 7:14898590 T ENSESTG00000023786 ENSESTT00000060125 Transcript intron_variant - - - - - - rs217545 7:14898590 T ENSESTG00000023786 ENSESTT00000060110 Transcript intron_variant - - - - - - rs217594 7:14937936 G ENSESTG00000023786 ENSESTT00000060076 Transcript intron_variant - - - - - - rs217594 7:14937936 G ENSESTG00000023786 ENSESTT00000060046 Transcript intron_variant - - - - - - rs217594 7:14937936 G ENSESTG00000023786 ENSESTT00000060125 Transcript intron_variant - - - - - - rs217594 7:14937936 G ENSESTG00000023786 ENSESTT00000060110 Transcript intron_variant - - - - - - rs6967637 7:15051310 G - - - intergenic_variant - - - - - - rs10257681 7:15063900 G - - - intergenic_variant - - - - - - rs7810290 7:15075782 A - - - intergenic_variant - - - - - - rs218073 7:15081904 G - ENSR00000622243 RegulatoryFeature regulatory_region_variant - - - - - - rs218073 7:15081904 G - - - intergenic_variant - - - - - - rs1981700 7:15101074 A - - - intergenic_variant - - - - - - rs2961262 7:15184387 G - - - intergenic_variant - - - - - - rs2908325 7:15196609 G - - - intergenic_variant - - - - - - rs10085513 7:15278034 A CCDS34604.1 CCDS34604.1 Transcript intron_variant - - - - - - rs10085513 7:15278034 A ENSESTG00000022064 ENSESTT00000055593 Transcript intron_variant - - - - - - rs10085513 7:15278034 A 392636 NM_001004320.1 Transcript intron_variant - - - - - - rs6960225 7:15745090 T ENSESTG00000021917 ENSESTT00000055101 Transcript upstream_gene_variant - - - - - - DISTANCE=3690 rs6960225 7:15745090 T ENSESTG00000021917 ENSESTT00000055117 Transcript upstream_gene_variant - - - - - - DISTANCE=3700 rs37424 7:15791590 C - - - intergenic_variant - - - - - - rs38254 7:15948351 G - - - intergenic_variant - - - - - - rs1548572 7:16366098 C ENSESTG00000024170 ENSESTT00000061225 Transcript intron_variant - - - - - - rs1548572 7:16366098 C ENSESTG00000024170 ENSESTT00000061240 Transcript intron_variant - - - - - - rs1548572 7:16366098 C 729920 NM_001101417.3 Transcript intron_variant - - - - - - rs1548572 7:16366098 C ENSESTG00000024170 ENSESTT00000061212 Transcript intron_variant - - - - - - rs1548572 7:16366098 C ENSESTG00000024170 ENSESTT00000061266 Transcript intron_variant - - - - - - rs1548572 7:16366098 C 729920 NM_001101426.3 Transcript intron_variant - - - - - - rs1548572 7:16366098 C ENSESTG00000024170 ENSESTT00000061244 Transcript intron_variant - - - - - - rs1548572 7:16366098 C ENSESTG00000024170 ENSESTT00000061276 Transcript intron_variant - - - - - - rs7794994 7:16982514 C - - - intergenic_variant - - - - - - rs4598144 7:16986132 G - - - intergenic_variant - - - - - - rs990322 7:17560814 A - ENSR00000622506 RegulatoryFeature regulatory_region_variant - - - - - - rs990322 7:17560814 A ENSESTG00000015798 ENSESTT00000039559 Transcript intron_variant - - - - - - rs4419718 7:17600239 T - ENSR00001557638 RegulatoryFeature regulatory_region_variant - - - - - - rs4419718 7:17600239 T ENSESTG00000015798 ENSESTT00000039559 Transcript upstream_gene_variant - - - - - - DISTANCE=1706 rs598308 7:18382302 A 9734 NM_001204144.1 Transcript intron_variant - - - - - - rs598308 7:18382302 A CCDS56465.1 CCDS56465.1 Transcript intron_variant - - - - - - rs2098997 7:18444796 C 9734 NM_001204144.1 Transcript intron_variant - - - - - - rs2098997 7:18444796 C CCDS56465.1 CCDS56465.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C - ENSR00001557702 RegulatoryFeature regulatory_region_variant - - - - - - rs801762 7:18560440 C ENSESTG00000016287 ENSESTT00000040973 Transcript intron_variant - - - - - - rs801762 7:18560440 C CCDS47557.1 CCDS47557.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C CCDS47555.1 CCDS47555.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C 9734 NM_001204146.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C 9734 NM_001204147.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C 9734 NM_014707.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C ENSESTG00000016287 ENSESTT00000040987 Transcript intron_variant - - - - - - rs801762 7:18560440 C ENSESTG00000016287 ENSESTT00000040929 Transcript intron_variant - - - - - - rs801762 7:18560440 C 9734 NM_001204144.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C ENSESTG00000016287 ENSESTT00000040941 Transcript intron_variant - - - - - - rs801762 7:18560440 C 9734 NM_058176.2 Transcript intron_variant - - - - - - rs801762 7:18560440 C ENSESTG00000016287 ENSESTT00000040981 Transcript intron_variant - - - - - - rs801762 7:18560440 C CCDS47553.1 CCDS47553.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C 9734 NM_178425.2 Transcript intron_variant - - - - - - rs801762 7:18560440 C 9734 NM_001204145.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C CCDS47554.1 CCDS47554.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C 9734 NM_001204148.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C 9734 NM_178423.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C ENSESTG00000016287 ENSESTT00000040993 Transcript intron_variant - - - - - - rs801762 7:18560440 C ENSESTG00000016287 ENSESTT00000040971 Transcript intron_variant - - - - - - rs801762 7:18560440 C CCDS56465.1 CCDS56465.1 Transcript intron_variant - - - - - - rs801762 7:18560440 C ENSESTG00000016287 ENSESTT00000040920 Transcript intron_variant - - - - - - rs801762 7:18560440 C CCDS56466.1 CCDS56466.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A ENSESTG00000016287 ENSESTT00000040973 Transcript intron_variant - - - - - - rs801536 7:18639033 A CCDS47557.1 CCDS47557.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A CCDS47555.1 CCDS47555.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A 9734 NM_001204146.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A 9734 NM_001204147.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A 9734 NM_014707.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A ENSESTG00000016287 ENSESTT00000040987 Transcript intron_variant - - - - - - rs801536 7:18639033 A ENSESTG00000016287 ENSESTT00000040929 Transcript intron_variant - - - - - - rs801536 7:18639033 A 9734 NM_001204144.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A 9734 NM_058176.2 Transcript intron_variant - - - - - - rs801536 7:18639033 A ENSESTG00000016287 ENSESTT00000041037 Transcript intron_variant - - - - - - rs801536 7:18639033 A CCDS47553.1 CCDS47553.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A 9734 NM_178425.2 Transcript intron_variant - - - - - - rs801536 7:18639033 A CCDS56468.1 CCDS56468.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A CCDS56467.1 CCDS56467.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A 9734 NM_001204145.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A CCDS47554.1 CCDS47554.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A 9734 NM_001204148.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A 9734 NM_178423.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A ENSESTG00000016287 ENSESTT00000040971 Transcript intron_variant - - - - - - rs801536 7:18639033 A ENSESTG00000016287 ENSESTT00000040993 Transcript intron_variant - - - - - - rs801536 7:18639033 A ENSESTG00000016287 ENSESTT00000041043 Transcript intron_variant - - - - - - rs801536 7:18639033 A CCDS56465.1 CCDS56465.1 Transcript intron_variant - - - - - - rs801536 7:18639033 A ENSESTG00000016287 ENSESTT00000040920 Transcript intron_variant - - - - - - rs801536 7:18639033 A CCDS56466.1 CCDS56466.1 Transcript intron_variant - - - - - - rs172476 7:18795532 C ENSESTG00000016287 ENSESTT00000040973 Transcript intron_variant - - - - - - rs172476 7:18795532 C CCDS47553.1 CCDS47553.1 Transcript intron_variant - - - - - - rs172476 7:18795532 C 9734 NM_178425.2 Transcript intron_variant - - - - - - rs172476 7:18795532 C CCDS47555.1 CCDS47555.1 Transcript intron_variant - - - - - - rs172476 7:18795532 C CCDS47554.1 CCDS47554.1 Transcript intron_variant - - - - - - rs172476 7:18795532 C 9734 NM_178423.1 Transcript intron_variant - - - - - - rs172476 7:18795532 C ENSESTG00000016287 ENSESTT00000040993 Transcript intron_variant - - - - - - rs172476 7:18795532 C ENSESTG00000016287 ENSESTT00000040971 Transcript intron_variant - - - - - - rs172476 7:18795532 C ENSESTG00000016287 ENSESTT00000040987 Transcript intron_variant - - - - - - rs172476 7:18795532 C ENSESTG00000016287 ENSESTT00000040929 Transcript intron_variant - - - - - - rs172476 7:18795532 C 9734 NM_058176.2 Transcript intron_variant - - - - - - rs172476 7:18795532 C ENSESTG00000016287 ENSESTT00000040920 Transcript intron_variant - - - - - - rs2853553 7:18979523 A CCDS47553.1 CCDS47553.1 Transcript intron_variant - - - - - - rs2853553 7:18979523 A 9734 NM_178425.2 Transcript intron_variant - - - - - - rs2853553 7:18979523 A CCDS47555.1 CCDS47555.1 Transcript intron_variant - - - - - - rs2853553 7:18979523 A CCDS47554.1 CCDS47554.1 Transcript intron_variant - - - - - - rs2853553 7:18979523 A 9734 NM_178423.1 Transcript intron_variant - - - - - - rs2853553 7:18979523 A ENSESTG00000016287 ENSESTT00000041050 Transcript intron_variant - - - - - - rs2853553 7:18979523 A ENSESTG00000016287 ENSESTT00000040971 Transcript intron_variant - - - - - - rs2853553 7:18979523 A ENSESTG00000016287 ENSESTT00000040987 Transcript intron_variant - - - - - - rs2853553 7:18979523 A 9734 NM_058176.2 Transcript intron_variant - - - - - - rs2853553 7:18979523 A ENSESTG00000016287 ENSESTT00000040920 Transcript intron_variant - - - - - - rs1859018 7:19102086 C - - - intergenic_variant - - - - - - rs2192479 7:19588508 G - - - intergenic_variant - - - - - - rs2215858 7:19594276 A - - - intergenic_variant - - - - - - rs10236436 7:20669040 A CCDS55090.1 CCDS55090.1 Transcript intron_variant - - - - - - rs10236436 7:20669040 A 340273 NM_001163941.1 Transcript intron_variant - - - - - - rs4721925 7:20671230 T CCDS55090.1 CCDS55090.1 Transcript intron_variant - - - - - - rs4721925 7:20671230 T 340273 NM_001163941.1 Transcript intron_variant - - - - - - rs12535128 7:20706645 T 340273 NM_001163993.1 Transcript 3_prime_UTR_variant 1182 - - - - - rs12535128 7:20706645 T ENSESTG00000012828 ENSESTT00000032172 Transcript upstream_gene_variant - - - - - - DISTANCE=1155 rs12535128 7:20706645 T CCDS55092.1 CCDS55092.1 Transcript downstream_gene_variant - - - - - - DISTANCE=255 rs12535128 7:20706645 T 340273 NM_001163941.1 Transcript intron_variant - - - - - - rs12535128 7:20706645 T CCDS55090.1 CCDS55090.1 Transcript intron_variant - - - - - - rs12535128 7:20706645 T CCDS5371.1 CCDS5371.1 Transcript intron_variant - - - - - - rs12535128 7:20706645 T 340273 NM_178559.5 Transcript intron_variant - - - - - - rs12535128 7:20706645 T ENSESTG00000012820 ENSESTT00000032152 Transcript intron_variant - - - - - - rs12537843 7:20706751 C 340273 NM_001163993.1 Transcript 3_prime_UTR_variant 1288 - - - - - rs12537843 7:20706751 C ENSESTG00000012828 ENSESTT00000032172 Transcript upstream_gene_variant - - - - - - DISTANCE=1261 rs12537843 7:20706751 C CCDS55092.1 CCDS55092.1 Transcript downstream_gene_variant - - - - - - DISTANCE=361 rs12537843 7:20706751 C 340273 NM_001163941.1 Transcript intron_variant - - - - - - rs12537843 7:20706751 C CCDS55090.1 CCDS55090.1 Transcript intron_variant - - - - - - rs12537843 7:20706751 C CCDS5371.1 CCDS5371.1 Transcript intron_variant - - - - - - rs12537843 7:20706751 C 340273 NM_178559.5 Transcript intron_variant - - - - - - rs12537843 7:20706751 C ENSESTG00000012820 ENSESTT00000032152 Transcript intron_variant - - - - - - rs4721934 7:20727890 A CCDS55090.1 CCDS55090.1 Transcript intron_variant - - - - - - rs4721934 7:20727890 A CCDS5371.1 CCDS5371.1 Transcript intron_variant - - - - - - rs4721934 7:20727890 A 340273 NM_001163941.1 Transcript intron_variant - - - - - - rs4721934 7:20727890 A 340273 NM_178559.5 Transcript intron_variant - - - - - - rs4719627 7:20787505 T CCDS55090.1 CCDS55090.1 Transcript intron_variant - - - - - - rs4719627 7:20787505 T ENSESTG00000012824 ENSESTT00000032156 Transcript downstream_gene_variant - - - - - - DISTANCE=4959 rs4719627 7:20787505 T CCDS5371.1 CCDS5371.1 Transcript intron_variant - - - - - - rs4719627 7:20787505 T 340273 NM_001163941.1 Transcript intron_variant - - - - - - rs4719627 7:20787505 T 340273 NM_178559.5 Transcript intron_variant - - - - - - rs1989377 7:21387465 G - - - intergenic_variant - - - - - - rs1859354 7:21491093 G ENSESTG00000020613 ENSESTT00000051802 Transcript intron_variant - - - - - - rs1859354 7:21491093 G ENSESTG00000020613 ENSESTT00000051778 Transcript intron_variant - - - - - - rs1859354 7:21491093 G 6671 NM_003112.3 Transcript intron_variant - - - - - - rs1859354 7:21491093 G CCDS5373.1 CCDS5373.1 Transcript intron_variant - - - - - - rs4722035 7:21569683 T - - - intergenic_variant - - - - - - rs2158876 7:22249233 A ENSESTG00000016076 ENSESTT00000040341 Transcript intron_variant - - - - - - rs2158876 7:22249233 A 9771 NM_012294.3 Transcript intron_variant - - - - - - rs2158876 7:22249233 A CCDS55093.1 CCDS55093.1 Transcript intron_variant - - - - - - rs2158876 7:22249233 A ENSESTG00000016076 ENSESTT00000040327 Transcript intron_variant - - - - - - rs2528922 7:22361244 A ENSESTG00000016076 ENSESTT00000040341 Transcript upstream_gene_variant - - - - - - DISTANCE=3588 rs2528922 7:22361244 A ENSESTG00000016076 ENSESTT00000040336 Transcript intron_variant - - - - - - rs2528922 7:22361244 A 9771 NM_012294.3 Transcript intron_variant - - - - - - rs2528922 7:22361244 A ENSESTG00000016076 ENSESTT00000040327 Transcript intron_variant - - - - - - rs4722160 7:22592948 G ENSESTG00000016056 ENSESTT00000040251 Transcript intron_variant - - - - - - rs4722160 7:22592948 G ENSESTG00000016056 ENSESTT00000040248 Transcript intron_variant - - - - - - rs7804305 7:22976579 A 84668 NM_032581.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4299 rs7804305 7:22976579 A ENSESTG00000033066 ENSESTT00000083572 Transcript intron_variant - - - - - - rs4562211 7:23033817 A ENSESTG00000033016 ENSESTT00000083547 Transcript intron_variant - - - - - - rs4562211 7:23033817 A ENSESTG00000033016 ENSESTT00000083526 Transcript intron_variant - - - - - - rs4562211 7:23033817 A ENSESTG00000033016 ENSESTT00000083554 Transcript intron_variant - - - - - - rs4562211 7:23033817 A ENSESTG00000033016 ENSESTT00000083539 Transcript intron_variant - - - - - - rs4562211 7:23033817 A 84668 NM_032581.3 Transcript intron_variant - - - - - - rs4562211 7:23033817 A CCDS5377.1 CCDS5377.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3087 rs6461698 7:23198160 A CCDS34609.1 CCDS34609.1 Transcript intron_variant - - - - - - rs6461698 7:23198160 A 55975 NM_018846.4 Transcript intron_variant - - - - - - rs6461698 7:23198160 A ENSESTG00000032666 ENSESTT00000082621 Transcript downstream_gene_variant - - - - - - DISTANCE=2374 rs6461698 7:23198160 A CCDS5378.2 CCDS5378.2 Transcript intron_variant - - - - - - rs6461698 7:23198160 A 55975 NR_033328.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6461698 7:23198160 A ENSESTG00000032666 ENSESTT00000082615 Transcript intron_variant - - - - - - rs6461698 7:23198160 A 55975 NM_001031710.2 Transcript intron_variant - - - - - - rs6461698 7:23198160 A ENSESTG00000032666 ENSESTT00000082608 Transcript intron_variant - - - - - - rs6461698 7:23198160 A ENSESTG00000032666 ENSESTT00000082617 Transcript downstream_gene_variant - - - - - - DISTANCE=2374 rs6461698 7:23198160 A ENSESTG00000032666 ENSESTT00000082632 Transcript intron_variant - - - - - - rs199661 7:23322071 G - - - intergenic_variant - - - - - - rs1013258 7:23938957 C ENSESTG00000032908 ENSESTT00000083235 Transcript intron_variant - - - - - - rs6942559 7:24488469 A - - - intergenic_variant - - - - - - rs6959499 7:24821288 T - - - intergenic_variant - - - - - - rs4722418 7:25075478 G - - - intergenic_variant - - - - - - rs6960723 7:26042987 A - - - intergenic_variant - - - - - - rs10279705 7:26279004 T - - - intergenic_variant - - - - - - rs10237602 7:26546781 G - - - intergenic_variant - - - - - - rs4719878 7:26748347 T 8935 NM_003930.3 Transcript intron_variant - - - - - - rs4719878 7:26748347 T ENSESTG00000023171 ENSESTT00000058694 Transcript intron_variant - - - - - - rs4719878 7:26748347 T ENSESTG00000023171 ENSESTT00000058771 Transcript intron_variant - - - - - - rs4719878 7:26748347 T ENSESTG00000023171 ENSESTT00000058728 Transcript intron_variant - - - - - - rs4719878 7:26748347 T ENSESTG00000023171 ENSESTT00000058677 Transcript intron_variant - - - - - - rs4719878 7:26748347 T CCDS5400.1 CCDS5400.1 Transcript intron_variant - - - - - - rs4719878 7:26748347 T ENSESTG00000023171 ENSESTT00000058791 Transcript intron_variant - - - - - - rs4719878 7:26748347 T ENSESTG00000023171 ENSESTT00000058731 Transcript intron_variant - - - - - - rs706016 7:27141267 T - ENSR00001558213 RegulatoryFeature regulatory_region_variant - - - - - - rs706016 7:27141267 T 3200 NM_153631.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4542 rs706016 7:27141267 T 3199 NM_006735.3 Transcript intron_variant - - - - - - rs706016 7:27141267 T 100506311 NR_038366.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1390 rs706016 7:27141267 T 100506311 NR_038367.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1390 rs706016 7:27141267 T 3200 NM_030661.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4542 rs706016 7:27141267 T CCDS5403.1 CCDS5403.1 Transcript intron_variant - - - - - - rs12537438 7:27287326 G CCDS5413.1 CCDS5413.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1282 rs12537438 7:27287326 G 2128 NM_001989.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1134 rs12537438 7:27287326 G ENSESTG00000032495 ENSESTT00000082016 Transcript downstream_gene_variant - - - - - - DISTANCE=1638 rs12537438 7:27287326 G ENSESTG00000032500 ENSESTT00000082024 Transcript intron_variant - - - - - - rs1229607 7:27634759 C CCDS5414.1 CCDS5414.1 Transcript intron_variant - - - - - - rs1229607 7:27634759 C 11112 NM_152740.3 Transcript intron_variant - - - - - - rs1229607 7:27634759 C ENSESTG00000032610 ENSESTT00000082370 Transcript intron_variant - - - - - - rs41293 7:28665831 G ENSESTG00000032127 ENSESTT00000081107 Transcript intron_variant - - - - - - rs41293 7:28665831 G 9586 NM_182899.3 Transcript intron_variant - - - - - - rs41293 7:28665831 G CCDS5418.1 CCDS5418.1 Transcript intron_variant - - - - - - rs41293 7:28665831 G 9586 NM_182898.2 Transcript intron_variant - - - - - - rs41293 7:28665831 G 9586 NM_004904.2 Transcript intron_variant - - - - - - rs41293 7:28665831 G CCDS43562.1 CCDS43562.1 Transcript intron_variant - - - - - - rs41293 7:28665831 G CCDS5417.1 CCDS5417.1 Transcript intron_variant - - - - - - rs41293 7:28665831 G ENSESTG00000032127 ENSESTT00000081146 Transcript intron_variant - - - - - - rs41293 7:28665831 G ENSESTG00000032127 ENSESTT00000081121 Transcript intron_variant - - - - - - rs6462101 7:28755868 T ENSESTG00000032127 ENSESTT00000081107 Transcript intron_variant - - - - - - rs6462101 7:28755868 T 9586 NM_182899.3 Transcript intron_variant - - - - - - rs6462101 7:28755868 T CCDS5418.1 CCDS5418.1 Transcript intron_variant - - - - - - rs6462101 7:28755868 T 9586 NM_182898.2 Transcript intron_variant - - - - - - rs6462101 7:28755868 T 9586 NM_004904.2 Transcript intron_variant - - - - - - rs6462101 7:28755868 T 9586 NM_001011666.1 Transcript intron_variant - - - - - - rs6462101 7:28755868 T CCDS43562.1 CCDS43562.1 Transcript intron_variant - - - - - - rs6462101 7:28755868 T CCDS5417.1 CCDS5417.1 Transcript intron_variant - - - - - - rs6462101 7:28755868 T ENSESTG00000032127 ENSESTT00000081195 Transcript intron_variant - - - - - - rs6462101 7:28755868 T ENSESTG00000032127 ENSESTT00000081146 Transcript intron_variant - - - - - - rs6462101 7:28755868 T CCDS43563.1 CCDS43563.1 Transcript intron_variant - - - - - - rs6462101 7:28755868 T ENSESTG00000032127 ENSESTT00000081121 Transcript intron_variant - - - - - - rs6462101 7:28755868 T ENSESTG00000032127 ENSESTT00000081187 Transcript intron_variant - - - - - - rs4722963 7:29967065 T CCDS47567.1 CCDS47567.1 Transcript intron_variant - - - - - - rs4722963 7:29967065 T ENSESTG00000010952 ENSESTT00000027501 Transcript intron_variant - - - - - - rs4722963 7:29967065 T CCDS5422.1 CCDS5422.1 Transcript intron_variant - - - - - - rs4722963 7:29967065 T 9805 NM_001145513.1 Transcript intron_variant - - - - - - rs4722963 7:29967065 T ENSESTG00000010952 ENSESTT00000027503 Transcript intron_variant - - - - - - rs4722963 7:29967065 T CCDS47568.1 CCDS47568.1 Transcript intron_variant - - - - - - rs4722963 7:29967065 T ENSESTG00000010952 ENSESTT00000027495 Transcript intron_variant - - - - - - rs4722963 7:29967065 T ENSESTG00000010459 ENSESTT00000026192 Transcript intron_variant - - - - - - rs4722963 7:29967065 T ENSESTG00000010952 ENSESTT00000027488 Transcript intron_variant - - - - - - rs4722963 7:29967065 T 9805 NM_014766.4 Transcript intron_variant - - - - - - rs4722963 7:29967065 T ENSESTG00000010952 ENSESTT00000027490 Transcript intron_variant - - - - - - rs4722963 7:29967065 T 9805 NM_001145515.1 Transcript intron_variant - - - - - - rs4722963 7:29967065 T 9805 NM_001145514.1 Transcript intron_variant - - - - - - rs12539305 7:30247331 T - - - intergenic_variant - - - - - - rs2391848 7:30313739 A - - - intergenic_variant - - - - - - rs42576 7:30380852 T ENSESTG00000010564 ENSESTT00000026441 Transcript intron_variant - - - - - - rs42576 7:30380852 T 223082 NM_147128.3 Transcript intron_variant - - - - - - rs42576 7:30380852 T CCDS5426.1 CCDS5426.1 Transcript intron_variant - - - - - - rs42577 7:30393990 G ENSESTG00000010564 ENSESTT00000026441 Transcript intron_variant - - - - - - rs42577 7:30393990 G 223082 NM_147128.3 Transcript intron_variant - - - - - - rs42577 7:30393990 G CCDS5426.1 CCDS5426.1 Transcript intron_variant - - - - - - rs6977388 7:31574629 C 223075 NM_001257968.1 Transcript intron_variant - - - - - - rs6977388 7:31574629 C ENSESTG00000008911 ENSESTT00000022397 Transcript intron_variant - - - - - - rs6977388 7:31574629 C ENSESTG00000008911 ENSESTT00000022378 Transcript intron_variant - - - - - - rs6977388 7:31574629 C ENSESTG00000008911 ENSESTT00000022386 Transcript intron_variant - - - - - - rs6977388 7:31574629 C ENSESTG00000008911 ENSESTT00000022389 Transcript intron_variant - - - - - - rs6977388 7:31574629 C CCDS59050.1 CCDS59050.1 Transcript intron_variant - - - - - - rs6977388 7:31574629 C 223075 NM_001257967.1 Transcript intron_variant - - - - - - rs6977388 7:31574629 C ENSESTG00000008911 ENSESTT00000022373 Transcript intron_variant - - - - - - rs6977388 7:31574629 C 223075 NR_047565.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2391997 7:31766920 C - - - intergenic_variant - - - - - - rs7786026 7:31876454 T 5137 NM_001191059.1 Transcript intron_variant - - - - - - rs7786026 7:31876454 T 5137 NM_001191057.1 Transcript intron_variant - - - - - - rs7786026 7:31876454 T ENSESTG00000015485 ENSESTT00000038820 Transcript intron_variant - - - - - - rs7786026 7:31876454 T 5137 NM_001191058.1 Transcript intron_variant - - - - - - rs7786026 7:31876454 T 5137 NM_001191056.1 Transcript intron_variant - - - - - - rs7786026 7:31876454 T ENSESTG00000015485 ENSESTT00000038867 Transcript intron_variant - - - - - - rs7786026 7:31876454 T ENSESTG00000015485 ENSESTT00000038835 Transcript intron_variant - - - - - - rs7786026 7:31876454 T CCDS5437.1 CCDS5437.1 Transcript intron_variant - - - - - - rs7786026 7:31876454 T ENSESTG00000015485 ENSESTT00000038847 Transcript intron_variant - - - - - - rs7786026 7:31876454 T 5137 NM_005020.2 Transcript intron_variant - - - - - - rs7786026 7:31876454 T CCDS55100.1 CCDS55100.1 Transcript intron_variant - - - - - - rs7786026 7:31876454 T ENSESTG00000015485 ENSESTT00000038871 Transcript intron_variant - - - - - - rs7786026 7:31876454 T CCDS55099.1 CCDS55099.1 Transcript intron_variant - - - - - - rs4404828 7:31903064 G 5137 NM_001191059.1 Transcript intron_variant - - - - - - rs4404828 7:31903064 G 5137 NM_001191057.1 Transcript intron_variant - - - - - - rs4404828 7:31903064 G ENSESTG00000015485 ENSESTT00000038820 Transcript intron_variant - - - - - - rs4404828 7:31903064 G 5137 NM_001191058.1 Transcript intron_variant - - - - - - rs4404828 7:31903064 G 5137 NM_001191056.1 Transcript intron_variant - - - - - - rs4404828 7:31903064 G ENSESTG00000015485 ENSESTT00000038867 Transcript intron_variant - - - - - - rs4404828 7:31903064 G ENSESTG00000015485 ENSESTT00000038835 Transcript intron_variant - - - - - - rs4404828 7:31903064 G CCDS5437.1 CCDS5437.1 Transcript intron_variant - - - - - - rs4404828 7:31903064 G ENSESTG00000015485 ENSESTT00000038847 Transcript intron_variant - - - - - - rs4404828 7:31903064 G 5137 NM_005020.2 Transcript intron_variant - - - - - - rs4404828 7:31903064 G CCDS55100.1 CCDS55100.1 Transcript intron_variant - - - - - - rs4404828 7:31903064 G ENSESTG00000015485 ENSESTT00000038871 Transcript intron_variant - - - - - - rs4404828 7:31903064 G CCDS55099.1 CCDS55099.1 Transcript intron_variant - - - - - - rs6462317 7:31998164 T - ENSR00000624288 RegulatoryFeature regulatory_region_variant - - - - - - rs6462317 7:31998164 T 5137 NM_001191059.1 Transcript intron_variant - - - - - - rs6462317 7:31998164 T 5137 NM_001191057.1 Transcript intron_variant - - - - - - rs6462317 7:31998164 T ENSESTG00000015485 ENSESTT00000038820 Transcript intron_variant - - - - - - rs6462317 7:31998164 T 5137 NM_001191058.1 Transcript intron_variant - - - - - - rs6462317 7:31998164 T 5137 NM_001191056.1 Transcript intron_variant - - - - - - rs6462317 7:31998164 T ENSESTG00000015485 ENSESTT00000038867 Transcript intron_variant - - - - - - rs6462317 7:31998164 T ENSESTG00000015485 ENSESTT00000038835 Transcript intron_variant - - - - - - rs6462317 7:31998164 T CCDS5437.1 CCDS5437.1 Transcript intron_variant - - - - - - rs6462317 7:31998164 T ENSESTG00000015485 ENSESTT00000038860 Transcript intron_variant - - - - - - rs6462317 7:31998164 T ENSESTG00000015485 ENSESTT00000038847 Transcript intron_variant - - - - - - rs6462317 7:31998164 T 5137 NM_005020.2 Transcript intron_variant - - - - - - rs6462317 7:31998164 T CCDS55100.1 CCDS55100.1 Transcript intron_variant - - - - - - rs6462317 7:31998164 T CCDS55099.1 CCDS55099.1 Transcript intron_variant - - - - - - rs30553 7:32053515 A 5137 NM_001191059.1 Transcript intron_variant - - - - - - rs30553 7:32053515 A 5137 NM_001191057.1 Transcript intron_variant - - - - - - rs30553 7:32053515 A ENSESTG00000015485 ENSESTT00000038820 Transcript intron_variant - - - - - - rs30553 7:32053515 A 5137 NM_001191058.1 Transcript intron_variant - - - - - - rs30553 7:32053515 A 5137 NM_001191056.1 Transcript intron_variant - - - - - - rs30553 7:32053515 A ENSESTG00000015485 ENSESTT00000038867 Transcript intron_variant - - - - - - rs30553 7:32053515 A ENSESTG00000015485 ENSESTT00000038835 Transcript intron_variant - - - - - - rs30553 7:32053515 A CCDS5437.1 CCDS5437.1 Transcript intron_variant - - - - - - rs30553 7:32053515 A ENSESTG00000015485 ENSESTT00000038860 Transcript intron_variant - - - - - - rs30553 7:32053515 A ENSESTG00000015485 ENSESTT00000038847 Transcript intron_variant - - - - - - rs30553 7:32053515 A 5137 NM_005020.2 Transcript intron_variant - - - - - - rs30553 7:32053515 A CCDS55100.1 CCDS55100.1 Transcript intron_variant - - - - - - rs30553 7:32053515 A CCDS55099.1 CCDS55099.1 Transcript intron_variant - - - - - - rs977625 7:32209425 G CCDS55100.1 CCDS55100.1 Transcript missense_variant 280 280 94 S/P Tca/Cca - PolyPhen=benign;SIFT=tolerated rs977625 7:32209425 G 5137 NM_001191058.1 Transcript missense_variant 316 280 94 S/P Tca/Cca - PolyPhen=benign;SIFT=tolerated rs4720056 7:32247626 A CCDS55100.1 CCDS55100.1 Transcript intron_variant - - - - - - rs4720056 7:32247626 A 5137 NM_001191058.1 Transcript intron_variant - - - - - - rs4236334 7:32271688 G CCDS55100.1 CCDS55100.1 Transcript intron_variant - - - - - - rs4236334 7:32271688 G 5137 NM_001191058.1 Transcript intron_variant - - - - - - rs1376304 7:32955405 A ENSESTG00000010329 ENSESTT00000025830 Transcript downstream_gene_variant - - - - - - DISTANCE=1713 rs1376304 7:32955405 A ENSESTG00000010329 ENSESTT00000025853 Transcript downstream_gene_variant - - - - - - DISTANCE=1626 rs1376304 7:32955405 A ENSESTG00000010329 ENSESTT00000025863 Transcript downstream_gene_variant - - - - - - DISTANCE=1627 rs1376304 7:32955405 A 441212 NR_003500.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1022 rs1376304 7:32955405 A ENSESTG00000010239 ENSESTT00000025605 Transcript downstream_gene_variant - - - - - - DISTANCE=1661 rs2598406 7:33599004 C - ENSR00001558691 RegulatoryFeature regulatory_region_variant - - - - - - rs2598406 7:33599004 C CCDS34618.1 CCDS34618.1 Transcript intron_variant - - - - - - rs2598406 7:33599004 C 27241 NM_198428.2 Transcript intron_variant - - - - - - rs2598406 7:33599004 C CCDS5441.1 CCDS5441.1 Transcript intron_variant - - - - - - rs2598406 7:33599004 C 27241 NM_001033605.1 Transcript intron_variant - - - - - - rs2598406 7:33599004 C ENSESTG00000010313 ENSESTT00000025800 Transcript intron_variant - - - - - - rs2598406 7:33599004 C 27241 NM_014451.3 Transcript intron_variant - - - - - - rs2598406 7:33599004 C 27241 NM_001033604.1 Transcript intron_variant - - - - - - rs2598406 7:33599004 C CCDS47572.1 CCDS47572.1 Transcript intron_variant - - - - - - rs2598406 7:33599004 C CCDS43566.1 CCDS43566.1 Transcript intron_variant - - - - - - rs2700682 7:33636206 G CCDS34618.1 CCDS34618.1 Transcript intron_variant - - - - - - rs2700682 7:33636206 G 27241 NM_198428.2 Transcript intron_variant - - - - - - rs2700682 7:33636206 G CCDS5441.1 CCDS5441.1 Transcript intron_variant - - - - - - rs2700682 7:33636206 G 27241 NM_001033605.1 Transcript intron_variant - - - - - - rs2700682 7:33636206 G ENSESTG00000010313 ENSESTT00000025800 Transcript intron_variant - - - - - - rs2700682 7:33636206 G 27241 NM_014451.3 Transcript intron_variant - - - - - - rs2700682 7:33636206 G 27241 NM_001033604.1 Transcript intron_variant - - - - - - rs2700682 7:33636206 G CCDS47572.1 CCDS47572.1 Transcript intron_variant - - - - - - rs2700682 7:33636206 G CCDS43566.1 CCDS43566.1 Transcript intron_variant - - - - - - rs3898751 7:33697835 T - - - intergenic_variant - - - - - - rs6462509 7:33801470 C - - - intergenic_variant - - - - - - rs9918583 7:33821140 C - - - intergenic_variant - - - - - - rs1345521 7:33822508 C - - - intergenic_variant - - - - - - rs1345522 7:33831935 C - ENSR00001558716 RegulatoryFeature regulatory_region_variant - - - - - - rs1345522 7:33831935 C ENSESTG00000006139 ENSESTT00000015460 Transcript downstream_gene_variant - - - - - - DISTANCE=921 rs2042093 7:33834714 A ENSESTG00000006139 ENSESTT00000015460 Transcript intron_variant - - - - - - rs968005 7:33879384 G - - - intergenic_variant - - - - - - rs10242187 7:33900895 G - - - intergenic_variant - - - - - - rs1013126 7:34706611 T 387129 NM_207172.1 Transcript intron_variant - - - - - - rs1013126 7:34706611 T CCDS5444.1 CCDS5444.1 Transcript intron_variant - - - - - - rs1013126 7:34706611 T CCDS5443.1 CCDS5443.1 Transcript intron_variant - - - - - - rs1013126 7:34706611 T ENSESTG00000006125 ENSESTT00000015440 Transcript intron_variant - - - - - - rs1013126 7:34706611 T 387129 NM_207173.1 Transcript intron_variant - - - - - - rs1013126 7:34706611 T 404744 NR_033665.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1013126 7:34706611 T 404744 NR_033664.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs740723 7:34866615 G CCDS5443.1 CCDS5443.1 Transcript intron_variant - - - - - - rs740723 7:34866615 G ENSESTG00000006125 ENSESTT00000015440 Transcript intron_variant - - - - - - rs740723 7:34866615 G 387129 NM_207173.1 Transcript intron_variant - - - - - - rs740723 7:34866615 G 404744 NR_015356.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs740723 7:34866615 G ENSESTG00000006131 ENSESTT00000015447 Transcript intron_variant - - - - - - rs740723 7:34866615 G 387129 NM_207172.1 Transcript intron_variant - - - - - - rs740723 7:34866615 G CCDS5444.1 CCDS5444.1 Transcript intron_variant - - - - - - rs740723 7:34866615 G ENSESTG00000008324 ENSESTT00000020997 Transcript upstream_gene_variant - - - - - - DISTANCE=483 rs1319503 7:34933000 G - - - intergenic_variant - - - - - - rs328933 7:35043123 G - ENSR00000624608 RegulatoryFeature regulatory_region_variant - - - - - - rs328933 7:35043123 G CCDS43567.1 CCDS43567.1 Transcript intron_variant - - - - - - rs328933 7:35043123 G ENSESTG00000008643 ENSESTT00000021789 Transcript upstream_gene_variant - - - - - - DISTANCE=2809 rs328933 7:35043123 G ENSESTG00000008643 ENSESTT00000021778 Transcript intron_variant - - - - - - rs328933 7:35043123 G ENSESTG00000008643 ENSESTT00000021794 Transcript upstream_gene_variant - - - - - - DISTANCE=2809 rs328933 7:35043123 G 23333 NM_015283.1 Transcript intron_variant - - - - - - rs328933 7:35043123 G ENSESTG00000008643 ENSESTT00000021788 Transcript intron_variant - - - - - - rs328933 7:35043123 G ENSESTG00000008643 ENSESTT00000021792 Transcript upstream_gene_variant - - - - - - DISTANCE=2809 rs328933 7:35043123 G ENSESTG00000008643 ENSESTT00000021782 Transcript intron_variant - - - - - - rs235393 7:35357526 C 401324 NR_038864.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs340386 7:35405917 C - ENSR00000624643 RegulatoryFeature regulatory_region_variant - - - - - - rs340386 7:35405917 C 401324 NR_038864.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2541904 7:35434242 A - - - intergenic_variant - - - - - - rs343017 7:35492014 T - - - intergenic_variant - - - - - - rs343065 7:35555323 G - - - intergenic_variant - - - - - - rs345398 7:35765888 C - - - intergenic_variant - - - - - - rs345392 7:35768378 G - ENSR00000624671 RegulatoryFeature regulatory_region_variant - - - - - - rs345392 7:35768378 G - - - intergenic_variant - - - - - - rs345390 7:35772065 C - - - intergenic_variant - - - - - - rs2252170 7:36067355 C - - - intergenic_variant - - - - - - rs6956244 7:36156387 A - ENSR00000624714 RegulatoryFeature regulatory_region_variant - - - - - - rs6956244 7:36156387 A - - - intergenic_variant - - - - - - rs2700890 7:36171426 A - - - intergenic_variant - - - - - - rs6462681 7:36561469 T CCDS5448.1 CCDS5448.1 Transcript intron_variant - - - - - - rs6462681 7:36561469 T 313 NM_001177506.1 Transcript intron_variant - - - - - - rs6462681 7:36561469 T CCDS55102.1 CCDS55102.1 Transcript intron_variant - - - - - - rs6462681 7:36561469 T 313 NM_001177507.1 Transcript intron_variant - - - - - - rs6462681 7:36561469 T 313 NM_001637.3 Transcript intron_variant - - - - - - rs2893532 7:36602296 C CCDS5448.1 CCDS5448.1 Transcript intron_variant - - - - - - rs2893532 7:36602296 C ENSESTG00000009554 ENSESTT00000024051 Transcript intron_variant - - - - - - rs2893532 7:36602296 C 313 NM_001177507.1 Transcript intron_variant - - - - - - rs2893532 7:36602296 C 313 NM_001637.3 Transcript intron_variant - - - - - - rs2893532 7:36602296 C 313 NM_001177506.1 Transcript intron_variant - - - - - - rs2893532 7:36602296 C ENSESTG00000009554 ENSESTT00000024056 Transcript intron_variant - - - - - - rs2893532 7:36602296 C CCDS55102.1 CCDS55102.1 Transcript intron_variant - - - - - - rs2893532 7:36602296 C ENSESTG00000009554 ENSESTT00000024048 Transcript intron_variant - - - - - - rs2893532 7:36602296 C ENSESTG00000009554 ENSESTT00000024059 Transcript intron_variant - - - - - - rs7791364 7:36946544 T 9844 NM_001039459.2 Transcript intron_variant - - - - - - rs7791364 7:36946544 T 9844 NM_001206480.1 Transcript intron_variant - - - - - - rs7791364 7:36946544 T ENSESTG00000015049 ENSESTT00000037751 Transcript intron_variant - - - - - - rs7791364 7:36946544 T 9844 NR_038120.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7791364 7:36946544 T ENSESTG00000015049 ENSESTT00000037742 Transcript intron_variant - - - - - - rs7791364 7:36946544 T 9844 NR_038121.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7791364 7:36946544 T ENSESTG00000015049 ENSESTT00000037726 Transcript intron_variant - - - - - - rs7791364 7:36946544 T ENSESTG00000015049 ENSESTT00000037736 Transcript intron_variant - - - - - - rs7791364 7:36946544 T ENSESTG00000015049 ENSESTT00000037763 Transcript intron_variant - - - - - - rs7791364 7:36946544 T ENSESTG00000015049 ENSESTT00000037741 Transcript intron_variant - - - - - - rs7791364 7:36946544 T 9844 NM_001206482.1 Transcript intron_variant - - - - - - rs7791364 7:36946544 T CCDS5449.1 CCDS5449.1 Transcript intron_variant - - - - - - rs7791364 7:36946544 T 9844 NM_014800.10 Transcript intron_variant - - - - - - rs6977999 7:36985867 G - ENSR00000624811 RegulatoryFeature regulatory_region_variant - - - - - - rs6977999 7:36985867 G 9844 NM_001039459.2 Transcript intron_variant - - - - - - rs6977999 7:36985867 G 9844 NM_001206480.1 Transcript intron_variant - - - - - - rs6977999 7:36985867 G ENSESTG00000015049 ENSESTT00000037751 Transcript intron_variant - - - - - - rs6977999 7:36985867 G 9844 NR_038120.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6977999 7:36985867 G ENSESTG00000015049 ENSESTT00000037742 Transcript intron_variant - - - - - - rs6977999 7:36985867 G 9844 NR_038121.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6977999 7:36985867 G ENSESTG00000015049 ENSESTT00000037726 Transcript intron_variant - - - - - - rs6977999 7:36985867 G ENSESTG00000015049 ENSESTT00000037736 Transcript intron_variant - - - - - - rs6977999 7:36985867 G ENSESTG00000015049 ENSESTT00000037763 Transcript intron_variant - - - - - - rs6977999 7:36985867 G ENSESTG00000015049 ENSESTT00000037741 Transcript intron_variant - - - - - - rs6977999 7:36985867 G 9844 NM_001206482.1 Transcript intron_variant - - - - - - rs6977999 7:36985867 G CCDS5449.1 CCDS5449.1 Transcript intron_variant - - - - - - rs6977999 7:36985867 G 9844 NM_014800.10 Transcript intron_variant - - - - - - rs7808870 7:36990850 T - ENSR00000624814 RegulatoryFeature regulatory_region_variant - - - - - - rs7808870 7:36990850 T 9844 NM_001039459.2 Transcript intron_variant - - - - - - rs7808870 7:36990850 T 9844 NM_001206480.1 Transcript intron_variant - - - - - - rs7808870 7:36990850 T ENSESTG00000015049 ENSESTT00000037751 Transcript intron_variant - - - - - - rs7808870 7:36990850 T 9844 NR_038120.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7808870 7:36990850 T ENSESTG00000015049 ENSESTT00000037742 Transcript intron_variant - - - - - - rs7808870 7:36990850 T 9844 NR_038121.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7808870 7:36990850 T ENSESTG00000015049 ENSESTT00000037726 Transcript intron_variant - - - - - - rs7808870 7:36990850 T ENSESTG00000015049 ENSESTT00000037736 Transcript intron_variant - - - - - - rs7808870 7:36990850 T ENSESTG00000015049 ENSESTT00000037763 Transcript intron_variant - - - - - - rs7808870 7:36990850 T ENSESTG00000015049 ENSESTT00000037741 Transcript intron_variant - - - - - - rs7808870 7:36990850 T 9844 NM_001206482.1 Transcript intron_variant - - - - - - rs7808870 7:36990850 T CCDS5449.1 CCDS5449.1 Transcript intron_variant - - - - - - rs7808870 7:36990850 T 9844 NM_014800.10 Transcript intron_variant - - - - - - rs929649 7:37224109 A 9844 NM_001206480.1 Transcript intron_variant - - - - - - rs929649 7:37224109 A ENSESTG00000015049 ENSESTT00000037726 Transcript intron_variant - - - - - - rs929649 7:37224109 A ENSESTG00000015049 ENSESTT00000037742 Transcript intron_variant - - - - - - rs929649 7:37224109 A ENSESTG00000015049 ENSESTT00000037736 Transcript intron_variant - - - - - - rs929649 7:37224109 A ENSESTG00000015049 ENSESTT00000037741 Transcript intron_variant - - - - - - rs929649 7:37224109 A 9844 NM_001206482.1 Transcript intron_variant - - - - - - rs929649 7:37224109 A 9844 NM_014800.10 Transcript intron_variant - - - - - - rs929649 7:37224109 A CCDS5449.1 CCDS5449.1 Transcript intron_variant - - - - - - rs2717958 7:37289096 C ENSESTG00000015093 ENSESTT00000037925 Transcript intron_variant - - - - - - rs2717958 7:37289096 C ENSESTG00000015093 ENSESTT00000037895 Transcript intron_variant - - - - - - rs2717958 7:37289096 C 9844 NM_001206480.1 Transcript intron_variant - - - - - - rs2717958 7:37289096 C ENSESTG00000015093 ENSESTT00000037864 Transcript intron_variant - - - - - - rs2717958 7:37289096 C ENSESTG00000015093 ENSESTT00000037928 Transcript intron_variant - - - - - - rs2717958 7:37289096 C ENSESTG00000015093 ENSESTT00000037860 Transcript intron_variant - - - - - - rs2717958 7:37289096 C ENSESTG00000015093 ENSESTT00000037878 Transcript intron_variant - - - - - - rs2717958 7:37289096 C ENSESTG00000015093 ENSESTT00000037885 Transcript intron_variant - - - - - - rs2717958 7:37289096 C 9844 NM_001206482.1 Transcript intron_variant - - - - - - rs2717958 7:37289096 C 9844 NM_014800.10 Transcript intron_variant - - - - - - rs2717958 7:37289096 C CCDS5449.1 CCDS5449.1 Transcript intron_variant - - - - - - rs2723956 7:37321957 T ENSESTG00000015093 ENSESTT00000037925 Transcript intron_variant - - - - - - rs2723956 7:37321957 T ENSESTG00000015093 ENSESTT00000037895 Transcript intron_variant - - - - - - rs2723956 7:37321957 T 9844 NM_001206480.1 Transcript intron_variant - - - - - - rs2723956 7:37321957 T ENSESTG00000015093 ENSESTT00000037864 Transcript intron_variant - - - - - - rs2723956 7:37321957 T ENSESTG00000015093 ENSESTT00000037928 Transcript intron_variant - - - - - - rs2723956 7:37321957 T ENSESTG00000015093 ENSESTT00000037860 Transcript intron_variant - - - - - - rs2723956 7:37321957 T ENSESTG00000015093 ENSESTT00000037878 Transcript intron_variant - - - - - - rs2723956 7:37321957 T ENSESTG00000015093 ENSESTT00000037885 Transcript intron_variant - - - - - - rs2723956 7:37321957 T 9844 NM_001206482.1 Transcript intron_variant - - - - - - rs2723956 7:37321957 T 9844 NM_014800.10 Transcript intron_variant - - - - - - rs2723956 7:37321957 T CCDS5449.1 CCDS5449.1 Transcript intron_variant - - - - - - rs2723957 7:37322046 T ENSESTG00000015093 ENSESTT00000037925 Transcript intron_variant - - - - - - rs2723957 7:37322046 T ENSESTG00000015093 ENSESTT00000037895 Transcript intron_variant - - - - - - rs2723957 7:37322046 T 9844 NM_001206480.1 Transcript intron_variant - - - - - - rs2723957 7:37322046 T ENSESTG00000015093 ENSESTT00000037864 Transcript intron_variant - - - - - - rs2723957 7:37322046 T ENSESTG00000015093 ENSESTT00000037928 Transcript intron_variant - - - - - - rs2723957 7:37322046 T ENSESTG00000015093 ENSESTT00000037860 Transcript intron_variant - - - - - - rs2723957 7:37322046 T ENSESTG00000015093 ENSESTT00000037878 Transcript intron_variant - - - - - - rs2723957 7:37322046 T ENSESTG00000015093 ENSESTT00000037885 Transcript intron_variant - - - - - - rs2723957 7:37322046 T 9844 NM_001206482.1 Transcript intron_variant - - - - - - rs2723957 7:37322046 T 9844 NM_014800.10 Transcript intron_variant - - - - - - rs2723957 7:37322046 T CCDS5449.1 CCDS5449.1 Transcript intron_variant - - - - - - rs2723963 7:37329531 T ENSESTG00000015093 ENSESTT00000037925 Transcript intron_variant - - - - - - rs2723963 7:37329531 T ENSESTG00000015093 ENSESTT00000037895 Transcript intron_variant - - - - - - rs2723963 7:37329531 T 9844 NM_001206480.1 Transcript intron_variant - - - - - - rs2723963 7:37329531 T ENSESTG00000015093 ENSESTT00000037864 Transcript intron_variant - - - - - - rs2723963 7:37329531 T ENSESTG00000015093 ENSESTT00000037928 Transcript intron_variant - - - - - - rs2723963 7:37329531 T ENSESTG00000015093 ENSESTT00000037860 Transcript intron_variant - - - - - - rs2723963 7:37329531 T ENSESTG00000015093 ENSESTT00000037878 Transcript intron_variant - - - - - - rs2723963 7:37329531 T ENSESTG00000015093 ENSESTT00000037885 Transcript intron_variant - - - - - - rs2723963 7:37329531 T 9844 NM_001206482.1 Transcript intron_variant - - - - - - rs2723963 7:37329531 T 9844 NM_014800.10 Transcript intron_variant - - - - - - rs2723963 7:37329531 T CCDS5449.1 CCDS5449.1 Transcript intron_variant - - - - - - rs2167161 7:37627916 A - - - intergenic_variant - - - - - - rs2717923 7:37707857 A - - - intergenic_variant - - - - - - rs2598110 7:37967367 T - ENSR00001558988 RegulatoryFeature regulatory_region_variant - - - - - - rs2598110 7:37967367 T ENSESTG00000024486 ENSESTT00000061939 Transcript intron_variant - - - - - - rs2598110 7:37967367 T ENSESTG00000015027 ENSESTT00000037653 Transcript intron_variant - - - - - - rs2598110 7:37967367 T CCDS59051.1 CCDS59051.1 Transcript intron_variant - - - - - - rs2598110 7:37967367 T ENSESTG00000025301 ENSESTT00000063814 Transcript intron_variant - - - - - - rs2598110 7:37967367 T CCDS5454.2 CCDS5454.2 Transcript intron_variant - - - - - - rs2598110 7:37967367 T CCDS59052.1 CCDS59052.1 Transcript intron_variant - - - - - - rs2598110 7:37967367 T 54749 NM_017549.4 Transcript intron_variant - - - - - - rs2598110 7:37967367 T 54749 NM_001242948.1 Transcript intron_variant - - - - - - rs2598110 7:37967367 T ENSESTG00000024486 ENSESTT00000062026 Transcript intron_variant - - - - - - rs2598110 7:37967367 T 54749 NM_001242946.1 Transcript intron_variant - - - - - - rs1450848 7:37992895 A ENSESTG00000024486 ENSESTT00000061939 Transcript downstream_gene_variant - - - - - - DISTANCE=4337 rs1450848 7:37992895 A ENSESTG00000015027 ENSESTT00000037653 Transcript downstream_gene_variant - - - - - - DISTANCE=2881 rs1450848 7:37992895 A CCDS59051.1 CCDS59051.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3090 rs1450848 7:37992895 A ENSESTG00000025301 ENSESTT00000063814 Transcript upstream_gene_variant - - - - - - DISTANCE=4417 rs1450848 7:37992895 A CCDS5454.2 CCDS5454.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2897 rs1450848 7:37992895 A CCDS59052.1 CCDS59052.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2897 rs1450848 7:37992895 A 54749 NM_017549.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1352 rs1450848 7:37992895 A 54749 NM_001242948.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1352 rs1450848 7:37992895 A ENSESTG00000024486 ENSESTT00000062026 Transcript downstream_gene_variant - - - - - - DISTANCE=1850 rs1450848 7:37992895 A 54749 NM_001242946.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1352 rs1608542 7:38190191 A - - - intergenic_variant - - - - - - rs6958300 7:38467923 G ENSESTG00000025180 ENSESTT00000063710 Transcript intron_variant - - - - - - rs6958300 7:38467923 G CCDS47574.1 CCDS47574.1 Transcript intron_variant - - - - - - rs6958300 7:38467923 G ENSESTG00000025180 ENSESTT00000063694 Transcript downstream_gene_variant - - - - - - DISTANCE=883 rs6958300 7:38467923 G ENSESTG00000025180 ENSESTT00000063673 Transcript intron_variant - - - - - - rs6958300 7:38467923 G 273 NM_001635.3 Transcript intron_variant - - - - - - rs6958300 7:38467923 G 273 NM_139316.2 Transcript intron_variant - - - - - - rs6958300 7:38467923 G CCDS5456.1 CCDS5456.1 Transcript intron_variant - - - - - - rs6960769 7:39174757 C 11281 NM_007252.3 Transcript intron_variant - - - - - - rs6960769 7:39174757 C CCDS55103.1 CCDS55103.1 Transcript intron_variant - - - - - - rs6960769 7:39174757 C 11281 NM_001166018.1 Transcript intron_variant - - - - - - rs6960769 7:39174757 C CCDS34620.2 CCDS34620.2 Transcript intron_variant - - - - - - rs6960769 7:39174757 C ENSESTG00000008770 ENSESTT00000022024 Transcript downstream_gene_variant - - - - - - DISTANCE=2511 rs6960769 7:39174757 C ENSESTG00000008770 ENSESTT00000022020 Transcript intron_variant - - - - - - rs6962243 7:39345379 A 11281 NM_007252.3 Transcript intron_variant - - - - - - rs6962243 7:39345379 A CCDS55103.1 CCDS55103.1 Transcript intron_variant - - - - - - rs6962243 7:39345379 A 11281 NM_001166018.1 Transcript intron_variant - - - - - - rs6962243 7:39345379 A CCDS34620.2 CCDS34620.2 Transcript intron_variant - - - - - - rs6962243 7:39345379 A ENSESTG00000008770 ENSESTT00000022020 Transcript intron_variant - - - - - - rs2159152 7:39404514 C 11281 NM_007252.3 Transcript intron_variant - - - - - - rs2159152 7:39404514 C CCDS55103.1 CCDS55103.1 Transcript intron_variant - - - - - - rs2159152 7:39404514 C 11281 NM_001166018.1 Transcript intron_variant - - - - - - rs2159152 7:39404514 C CCDS34620.2 CCDS34620.2 Transcript intron_variant - - - - - - rs6462915 7:39440952 A 11281 NM_007252.3 Transcript intron_variant - - - - - - rs6462915 7:39440952 A CCDS55103.1 CCDS55103.1 Transcript intron_variant - - - - - - rs6462915 7:39440952 A 11281 NM_001166018.1 Transcript intron_variant - - - - - - rs6462915 7:39440952 A CCDS34620.2 CCDS34620.2 Transcript intron_variant - - - - - - rs6462915 7:39440952 A 100861520 NR_046711.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3245 rs1990245 7:39513449 G ENSESTG00000008783 ENSESTT00000022049 Transcript intron_variant - - - - - - rs773391 7:39976958 T - - - intergenic_variant - - - - - - rs6462971 7:40352602 C 79783 NM_001193313.1 Transcript intron_variant - - - - - - rs6462971 7:40352602 C 79783 NM_024728.2 Transcript intron_variant - - - - - - rs6462971 7:40352602 C CCDS55105.1 CCDS55105.1 Transcript intron_variant - - - - - - rs6462971 7:40352602 C CCDS55104.1 CCDS55104.1 Transcript intron_variant - - - - - - rs6462971 7:40352602 C 79783 NM_001193311.1 Transcript intron_variant - - - - - - rs6462971 7:40352602 C CCDS55106.1 CCDS55106.1 Transcript intron_variant - - - - - - rs6462971 7:40352602 C 79783 NM_001193312.1 Transcript intron_variant - - - - - - rs1034803 7:40524476 G 79783 NM_001193313.1 Transcript intron_variant - - - - - - rs1034803 7:40524476 G 79783 NM_024728.2 Transcript intron_variant - - - - - - rs1034803 7:40524476 G CCDS55105.1 CCDS55105.1 Transcript intron_variant - - - - - - rs1034803 7:40524476 G CCDS55104.1 CCDS55104.1 Transcript intron_variant - - - - - - rs1034803 7:40524476 G 79783 NM_001193311.1 Transcript intron_variant - - - - - - rs1034803 7:40524476 G CCDS55106.1 CCDS55106.1 Transcript intron_variant - - - - - - rs1034803 7:40524476 G 79783 NM_001193312.1 Transcript intron_variant - - - - - - rs4720369 7:40629454 T 79783 NM_001193313.1 Transcript intron_variant - - - - - - rs4720369 7:40629454 T 79783 NM_024728.2 Transcript intron_variant - - - - - - rs4720369 7:40629454 T CCDS55105.1 CCDS55105.1 Transcript intron_variant - - - - - - rs4720369 7:40629454 T CCDS55104.1 CCDS55104.1 Transcript intron_variant - - - - - - rs4720369 7:40629454 T 79783 NM_001193311.1 Transcript intron_variant - - - - - - rs4720369 7:40629454 T CCDS55106.1 CCDS55106.1 Transcript intron_variant - - - - - - rs4720369 7:40629454 T 79783 NM_001193312.1 Transcript intron_variant - - - - - - rs1990132 7:41706231 C ENSESTG00000028734 ENSESTT00000072285 Transcript downstream_gene_variant - - - - - - DISTANCE=553 rs6463081 7:42009899 C CCDS5465.1 CCDS5465.1 Transcript intron_variant - - - - - - rs6463081 7:42009899 C 2737 NM_000168.5 Transcript intron_variant - - - - - - rs6463081 7:42009899 C ENSESTG00000002597 ENSESTT00000006446 Transcript upstream_gene_variant - - - - - - DISTANCE=2348 rs799090 7:43018271 G ENSESTG00000017861 ENSESTT00000044971 Transcript intron_variant - - - - - - rs1034842 7:43751393 C 55744 NM_018224.3 Transcript intron_variant - - - - - - rs1034842 7:43751393 C 55744 NR_047701.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1034842 7:43751393 C ENSESTG00000017799 ENSESTT00000044918 Transcript intron_variant - - - - - - rs1034842 7:43751393 C ENSESTG00000017799 ENSESTT00000044929 Transcript intron_variant - - - - - - rs673286 7:43905910 C 100534592 NM_001204871.1 Transcript downstream_gene_variant - - - - - - DISTANCE=247 rs673286 7:43905910 C ENSESTG00000013843 ENSESTT00000034613 Transcript downstream_gene_variant - - - - - - DISTANCE=246 rs673286 7:43905910 C CCDS5473.1 CCDS5473.1 Transcript downstream_gene_variant - - - - - - DISTANCE=388 rs673286 7:43905910 C 64951 NM_032014.2 Transcript downstream_gene_variant - - - - - - DISTANCE=247 rs673286 7:43905910 C ENSESTG00000013843 ENSESTT00000034607 Transcript downstream_gene_variant - - - - - - DISTANCE=246 rs2730615 7:43915046 A 55665 NM_001077664.1 Transcript downstream_gene_variant - - - - - - DISTANCE=455 rs2730615 7:43915046 A ENSESTG00000013831 ENSESTT00000034572 Transcript downstream_gene_variant - - - - - - DISTANCE=3307 rs2730615 7:43915046 A 100534592 NM_001204871.1 Transcript intron_variant - - - - - - rs2730615 7:43915046 A CCDS43572.1 CCDS43572.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1220 rs2730615 7:43915046 A 55665 NM_001077663.1 Transcript downstream_gene_variant - - - - - - DISTANCE=455 rs2730615 7:43915046 A CCDS47577.1 CCDS47577.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1220 rs2730615 7:43915046 A ENSESTG00000013219 ENSESTT00000033155 Transcript upstream_gene_variant - - - - - - DISTANCE=3109 rs2730615 7:43915046 A ENSESTG00000013831 ENSESTT00000034578 Transcript downstream_gene_variant - - - - - - DISTANCE=3307 rs2730615 7:43915046 A 55665 NM_017920.3 Transcript downstream_gene_variant - - - - - - DISTANCE=455 rs2730615 7:43915046 A CCDS47578.1 CCDS47578.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1220 rs2007983 7:44235081 G - - - intergenic_variant - - - - - - rs12674197 7:44883548 A CCDS5498.1 CCDS5498.1 Transcript intron_variant - - - - - - rs12674197 7:44883548 A ENSESTG00000004724 ENSESTT00000011975 Transcript intron_variant - - - - - - rs12674197 7:44883548 A CCDS47581.1 CCDS47581.1 Transcript intron_variant - - - - - - rs12674197 7:44883548 A ENSESTG00000004599 ENSESTT00000011591 Transcript upstream_gene_variant - - - - - - DISTANCE=4467 rs12674197 7:44883548 A CCDS5496.1 CCDS5496.1 Transcript intron_variant - - - - - - rs12674197 7:44883548 A 94239 NM_012412.4 Transcript intron_variant - - - - - - rs12674197 7:44883548 A CCDS5497.1 CCDS5497.1 Transcript intron_variant - - - - - - rs12674197 7:44883548 A 94239 NM_201517.2 Transcript intron_variant - - - - - - rs12674197 7:44883548 A 94239 NM_201516.2 Transcript intron_variant - - - - - - rs12674197 7:44883548 A CCDS5495.1 CCDS5495.1 Transcript intron_variant - - - - - - rs12674197 7:44883548 A 94239 NM_138635.3 Transcript intron_variant - - - - - - rs12674197 7:44883548 A 94239 NM_201436.2 Transcript intron_variant - - - - - - rs12674197 7:44883548 A ENSESTG00000004724 ENSESTT00000011991 Transcript intron_variant - - - - - - rs4454204 7:45424352 G - - - intergenic_variant - - - - - - rs1464892 7:45495462 G - ENSR00000625846 RegulatoryFeature regulatory_region_variant - - - - - - rs1464892 7:45495462 G - - - intergenic_variant - - - - - - rs2471262 7:45709627 T CCDS34631.1 CCDS34631.1 Transcript intron_variant - - - - - - rs2471262 7:45709627 T 107 NM_021116.2 Transcript intron_variant - - - - - - rs1872590 7:46203407 C - - - intergenic_variant - - - - - - rs11769138 7:46593153 C - - - intergenic_variant - - - - - - rs1404718 7:46815760 G - ENSR00001559730 RegulatoryFeature regulatory_region_variant - - - - - - rs1404718 7:46815760 G - - - intergenic_variant - - - - - - rs2190015 7:46945075 C ENSESTG00000031435 ENSESTT00000079321 Transcript intron_variant - - - - - - rs2964964 7:47538563 T - ENSR00001559807 RegulatoryFeature regulatory_region_variant - - - - - - rs2964964 7:47538563 T ENSESTG00000031258 ENSESTT00000078917 Transcript intron_variant - - - - - - rs2964964 7:47538563 T 64759 NM_022748.11 Transcript intron_variant - - - - - - rs2964964 7:47538563 T ENSESTG00000031258 ENSESTT00000078875 Transcript intron_variant - - - - - - rs10081309 7:47645771 G - - - intergenic_variant - - - - - - rs2708863 7:48011879 T ENSESTG00000021787 ENSESTT00000055023 Transcript intron_variant - - - - - - rs2708863 7:48011879 T 3364 NM_004507.3 Transcript intron_variant - - - - - - rs2708863 7:48011879 T ENSESTG00000021787 ENSESTT00000055084 Transcript intron_variant - - - - - - rs2708863 7:48011879 T ENSESTG00000021787 ENSESTT00000055096 Transcript intron_variant - - - - - - rs2708863 7:48011879 T ENSESTG00000021787 ENSESTT00000055047 Transcript intron_variant - - - - - - rs2708863 7:48011879 T ENSESTG00000021787 ENSESTT00000055000 Transcript intron_variant - - - - - - rs2708863 7:48011879 T CCDS34635.1 CCDS34635.1 Transcript intron_variant - - - - - - rs2708863 7:48011879 T 3364 NR_037917.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2708863 7:48011879 T ENSESTG00000021787 ENSESTT00000055079 Transcript intron_variant - - - - - - rs141055781 7:48233552 G ENSESTG00000021439 ENSESTT00000053789 Transcript intron_variant - - - - - - rs141055781 7:48233552 G CCDS47584.1 CCDS47584.1 Transcript intron_variant - - - - - - rs141055781 7:48233552 G 154664 NM_152701.3 Transcript intron_variant - - - - - - rs6583459 7:48282985 A CCDS47584.1 CCDS47584.1 Transcript intron_variant - - - - - - rs6583459 7:48282985 A 154664 NM_152701.3 Transcript intron_variant - - - - - - rs6583448 7:48545976 G CCDS47584.1 CCDS47584.1 Transcript missense_variant 13336 13336 4446 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs6583448 7:48545976 G 154664 NM_152701.3 Transcript missense_variant 13360 13336 4446 K/E Aag/Gag - PolyPhen=benign;SIFT=tolerated rs6583448 7:48545976 G ENSESTG00000021505 ENSESTT00000053980 Transcript upstream_gene_variant - - - - - - DISTANCE=1494 rs1527841 7:48582753 A ENSESTG00000021530 ENSESTT00000054064 Transcript intron_variant - - - - - - rs1527841 7:48582753 A ENSESTG00000021530 ENSESTT00000054055 Transcript intron_variant - - - - - - rs1527841 7:48582753 A CCDS47584.1 CCDS47584.1 Transcript intron_variant - - - - - - rs1527841 7:48582753 A 154664 NM_152701.3 Transcript intron_variant - - - - - - rs7793785 7:48622427 T ENSESTG00000021530 ENSESTT00000054064 Transcript intron_variant - - - - - - rs7793785 7:48622427 T ENSESTG00000021530 ENSESTT00000054055 Transcript intron_variant - - - - - - rs7793785 7:48622427 T CCDS47584.1 CCDS47584.1 Transcript intron_variant - - - - - - rs7793785 7:48622427 T 154664 NM_152701.3 Transcript intron_variant - - - - - - rs10269894 7:48742169 A - - - intergenic_variant - - - - - - rs12540399 7:48764822 G - - - intergenic_variant - - - - - - rs28808 7:48918137 G - - - intergenic_variant - - - - - - rs7787897 7:48972924 G - - - intergenic_variant - - - - - - rs12718236 7:50109183 T - ENSR00001048910 RegulatoryFeature regulatory_region_variant - - - - - - rs12718236 7:50109183 T CCDS5509.1 CCDS5509.1 Transcript intron_variant - - - - - - rs12718236 7:50109183 T CCDS55110.1 CCDS55110.1 Transcript intron_variant - - - - - - rs12718236 7:50109183 T 11055 NM_001159878.1 Transcript intron_variant - - - - - - rs12718236 7:50109183 T 11055 NM_007009.2 Transcript intron_variant - - - - - - rs12718236 7:50109183 T ENSESTG00000005083 ENSESTT00000012942 Transcript intron_variant - - - - - - rs1917266 7:51525624 C - - - intergenic_variant - - - - - - rs1880427 7:51529881 G - - - intergenic_variant - - - - - - rs7776944 7:51568156 G - - - intergenic_variant - - - - - - rs6960770 7:51683100 G ENSESTG00000030342 ENSESTT00000076373 Transcript intron_variant - - - - - - rs1238376 7:52788651 A - - - intergenic_variant - - - - - - rs1230518 7:52836128 C - - - intergenic_variant - - - - - - rs7782020 7:52971981 C - - - intergenic_variant - - - - - - rs1174841 7:53078681 C - - - intergenic_variant - - - - - - rs10243737 7:53389899 T - - - intergenic_variant - - - - - - rs1534732 7:53880296 A ENSESTG00000005618 ENSESTT00000014257 Transcript upstream_gene_variant - - - - - - DISTANCE=672 rs1534732 7:53880296 A 401337 NR_038371.1 Transcript upstream_gene_variant - - - - - - DISTANCE=672 rs10278878 7:54305125 A - - - intergenic_variant - - - - - - rs519635 7:54741371 A - - - intergenic_variant - - - - - - rs10243865 7:55108832 G - ENSR00000626732 RegulatoryFeature regulatory_region_variant - - - - - - rs10243865 7:55108832 G 1956 NM_201283.1 Transcript intron_variant - - - - - - rs10243865 7:55108832 G ENSESTG00000033887 ENSESTT00000085772 Transcript intron_variant - - - - - - rs10243865 7:55108832 G 1956 NM_201284.1 Transcript intron_variant - - - - - - rs10243865 7:55108832 G 1956 NM_005228.3 Transcript intron_variant - - - - - - rs10243865 7:55108832 G CCDS5516.1 CCDS5516.1 Transcript intron_variant - - - - - - rs10243865 7:55108832 G CCDS5515.1 CCDS5515.1 Transcript intron_variant - - - - - - rs10243865 7:55108832 G CCDS5514.1 CCDS5514.1 Transcript intron_variant - - - - - - rs10243865 7:55108832 G 1956 NM_201282.1 Transcript intron_variant - - - - - - rs10243865 7:55108832 G CCDS47587.1 CCDS47587.1 Transcript intron_variant - - - - - - rs10243865 7:55108832 G ENSESTG00000033887 ENSESTT00000085774 Transcript intron_variant - - - - - - rs6593259 7:55638863 G - ENSR00000626878 RegulatoryFeature regulatory_region_variant - - - - - - rs6593259 7:55638863 G CCDS47588.1 CCDS47588.1 Transcript intron_variant - - - - - - rs6593259 7:55638863 G ENSESTG00000033966 ENSESTT00000085874 Transcript intron_variant - - - - - - rs6593259 7:55638863 G ENSESTG00000033966 ENSESTT00000085866 Transcript intron_variant - - - - - - rs6593259 7:55638863 G ENSESTG00000033966 ENSESTT00000085847 Transcript intron_variant - - - - - - rs6593259 7:55638863 G ENSESTG00000033966 ENSESTT00000085871 Transcript intron_variant - - - - - - rs6593259 7:55638863 G 81552 NM_030796.3 Transcript intron_variant - - - - - - rs6593259 7:55638863 G ENSESTG00000033966 ENSESTT00000085865 Transcript intron_variant - - - - - - rs6593259 7:55638863 G ENSESTG00000033966 ENSESTT00000085872 Transcript intron_variant - - - - - - rs4286899 7:55641784 A - ENSR00001560217 RegulatoryFeature regulatory_region_variant - - - - - - rs4286899 7:55641784 A CCDS47588.1 CCDS47588.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1767 rs4286899 7:55641784 A ENSESTG00000033966 ENSESTT00000085874 Transcript upstream_gene_variant - - - - - - DISTANCE=2247 rs4286899 7:55641784 A ENSESTG00000033966 ENSESTT00000085866 Transcript upstream_gene_variant - - - - - - DISTANCE=1631 rs4286899 7:55641784 A ENSESTG00000033966 ENSESTT00000085847 Transcript upstream_gene_variant - - - - - - DISTANCE=1103 rs4286899 7:55641784 A ENSESTG00000033966 ENSESTT00000085871 Transcript upstream_gene_variant - - - - - - DISTANCE=1637 rs4286899 7:55641784 A 81552 NM_030796.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1584 rs4286899 7:55641784 A ENSESTG00000033966 ENSESTT00000085865 Transcript upstream_gene_variant - - - - - - DISTANCE=1629 rs4286899 7:55641784 A ENSESTG00000033966 ENSESTT00000085872 Transcript upstream_gene_variant - - - - - - DISTANCE=2223 rs7801348 7:55693139 T - - - intergenic_variant - - - - - - rs816243 7:56230956 C - - - intergenic_variant - - - - - - rs7782881 7:56670331 A - - - intergenic_variant - - - - - - rs6557575 7:57439011 G - - - intergenic_variant - - - - - - rs1825337 7:57825451 A ENSESTG00000017244 ENSESTT00000043302 Transcript downstream_gene_variant - - - - - - DISTANCE=3075 rs2624950 7:63247530 A - - - intergenic_variant - - - - - - rs2082659 7:63627943 G - - - intergenic_variant - - - - - - rs593524 7:63861537 G - - - intergenic_variant - - - - - - rs7792621 7:64071382 T - - - intergenic_variant - - - - - - rs6946253 7:64277953 C 7697 NR_027661.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6946253 7:64277953 C ENSESTG00000007729 ENSESTT00000019497 Transcript intron_variant - - - - - - rs6946253 7:64277953 C ENSESTG00000007729 ENSESTT00000019517 Transcript intron_variant - - - - - - rs6946253 7:64277953 C CCDS34645.2 CCDS34645.2 Transcript intron_variant - - - - - - rs6946253 7:64277953 C ENSESTG00000007729 ENSESTT00000019501 Transcript intron_variant - - - - - - rs6946253 7:64277953 C ENSESTG00000007729 ENSESTT00000019511 Transcript intron_variant - - - - - - rs6946253 7:64277953 C 7697 NR_027660.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6946253 7:64277953 C ENSESTG00000007729 ENSESTT00000019493 Transcript intron_variant - - - - - - rs6946253 7:64277953 C ENSESTG00000007729 ENSESTT00000019526 Transcript intron_variant - - - - - - rs6946253 7:64277953 C 7697 NM_006524.2 Transcript intron_variant - - - - - - rs6946253 7:64277953 C CCDS55115.1 CCDS55115.1 Transcript intron_variant - - - - - - rs6946253 7:64277953 C ENSESTG00000007729 ENSESTT00000019488 Transcript intron_variant - - - - - - rs6946253 7:64277953 C 7697 NM_001160183.1 Transcript intron_variant - - - - - - rs7788396 7:64314079 A ENSESTG00000007729 ENSESTT00000019511 Transcript downstream_gene_variant - - - - - - DISTANCE=1623 rs7788396 7:64314079 A ENSESTG00000007729 ENSESTT00000019536 Transcript downstream_gene_variant - - - - - - DISTANCE=1417 rs7797780 7:64345737 G ENSESTG00000007750 ENSESTT00000019554 Transcript intron_variant - - - - - - rs10085423 7:64374164 C CCDS5528.2 CCDS5528.2 Transcript intron_variant - - - - - - rs10085423 7:64374164 C 10793 NM_021148.2 Transcript intron_variant - - - - - - rs10085423 7:64374164 C ENSESTG00000007754 ENSESTT00000019628 Transcript intron_variant - - - - - - rs10085423 7:64374164 C ENSESTG00000007754 ENSESTT00000019636 Transcript intron_variant - - - - - - rs10085423 7:64374164 C ENSESTG00000007754 ENSESTT00000019611 Transcript intron_variant - - - - - - rs10085423 7:64374164 C 10793 NR_003099.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2177664 7:64454478 G 2086 NM_001007253.3 Transcript intron_variant - - - - - - rs2177664 7:64454478 G CCDS47595.1 CCDS47595.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1074 rs2177664 7:64454478 G 51351 NM_015852.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3064 rs1531960 7:64699639 G - - - intergenic_variant - - - - - - rs601488 7:64777185 T - - - intergenic_variant - - - - - - rs6964295 7:64792418 A - - - intergenic_variant - - - - - - rs9987034 7:64862866 G - ENSR00001560313 RegulatoryFeature regulatory_region_variant - - - - - - rs9987034 7:64862866 G 168374 NM_007139.2 Transcript intron_variant - - - - - - rs9987034 7:64862866 G CCDS34646.1 CCDS34646.1 Transcript intron_variant - - - - - - rs9987034 7:64862866 G ENSESTG00000022422 ENSESTT00000056783 Transcript intron_variant - - - - - - rs9987034 7:64862866 G CCDS47596.1 CCDS47596.1 Transcript intron_variant - - - - - - rs9987034 7:64862866 G ENSESTG00000022422 ENSESTT00000056797 Transcript intron_variant - - - - - - rs9987034 7:64862866 G 168374 NM_152626.2 Transcript intron_variant - - - - - - rs2015855 7:64936891 G - - - intergenic_variant - - - - - - rs1815104 7:65276359 G - - - intergenic_variant - - - - - - rs160654 7:65535561 G - - - intergenic_variant - - - - - - rs6960150 7:65991272 C ENSESTG00000007253 ENSESTT00000018323 Transcript intron_variant - - - - - - rs758677 7:66091506 C - ENSR00000627508 RegulatoryFeature regulatory_region_variant - - - - - - rs758677 7:66091506 C CCDS55117.1 CCDS55117.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2546 rs758677 7:66091506 C ENSESTG00000007061 ENSESTT00000017890 Transcript upstream_gene_variant - - - - - - DISTANCE=2384 rs758677 7:66091506 C CCDS5534.1 CCDS5534.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2546 rs758677 7:66091506 C 154881 NM_001167961.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2362 rs758677 7:66091506 C 154881 NM_153033.4 Transcript upstream_gene_variant - - - - - - DISTANCE=2362 rs2707825 7:66175315 A - - - intergenic_variant - - - - - - rs4718399 7:66231648 C ENSESTG00000007102 ENSESTT00000017992 Transcript intron_variant - - - - - - rs4718399 7:66231648 C ENSESTG00000007102 ENSESTT00000017996 Transcript upstream_gene_variant - - - - - - DISTANCE=4819 rs4718399 7:66231648 C 27342 NM_014504.2 Transcript intron_variant - - - - - - rs6970242 7:66291831 G 729156 NR_003934.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10265576 7:66297039 C ENSESTG00000007242 ENSESTT00000018257 Transcript downstream_gene_variant - - - - - - DISTANCE=309 rs10265576 7:66297039 C ENSESTG00000007242 ENSESTT00000018254 Transcript downstream_gene_variant - - - - - - DISTANCE=244 rs10265576 7:66297039 C 729156 NR_003934.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1404980 7:66420988 C ENSESTG00000007237 ENSESTT00000018237 Transcript intron_variant - - - - - - rs1404980 7:66420988 C ENSESTG00000007142 ENSESTT00000018046 Transcript downstream_gene_variant - - - - - - DISTANCE=2654 rs1404980 7:66420988 C 55069 NM_017994.4 Transcript 3_prime_UTR_variant 1688 - - - - - rs1404980 7:66420988 C ENSESTG00000007142 ENSESTT00000018051 Transcript downstream_gene_variant - - - - - - DISTANCE=2654 rs1404980 7:66420988 C ENSESTG00000007142 ENSESTT00000018057 Transcript downstream_gene_variant - - - - - - DISTANCE=2654 rs1404980 7:66420988 C CCDS5536.1 CCDS5536.1 Transcript downstream_gene_variant - - - - - - DISTANCE=479 rs10807708 7:66485559 C CCDS5538.1 CCDS5538.1 Transcript intron_variant - - - - - - rs10807708 7:66485559 C ENSESTG00000007154 ENSESTT00000018133 Transcript downstream_gene_variant - - - - - - DISTANCE=2691 rs10807708 7:66485559 C 55253 NM_018264.2 Transcript intron_variant - - - - - - rs10807708 7:66485559 C ENSESTG00000007154 ENSESTT00000018123 Transcript intron_variant - - - - - - rs10807708 7:66485559 C ENSESTG00000007154 ENSESTT00000018146 Transcript intron_variant - - - - - - rs4117662 7:66560931 C CCDS5538.1 CCDS5538.1 Transcript intron_variant - - - - - - rs4117662 7:66560931 C ENSESTG00000007154 ENSESTT00000018200 Transcript intron_variant - - - - - - rs4117662 7:66560931 C ENSESTG00000007154 ENSESTT00000018203 Transcript intron_variant - - - - - - rs4117662 7:66560931 C 55253 NM_018264.2 Transcript intron_variant - - - - - - rs4718574 7:66927625 C - - - intergenic_variant - - - - - - rs12698644 7:67438838 T - - - intergenic_variant - - - - - - rs4349877 7:67475201 G - - - intergenic_variant - - - - - - rs2527628 7:68271287 T - - - intergenic_variant - - - - - - rs4718834 7:68434560 G - - - intergenic_variant - - - - - - rs3102815 7:68545730 C - - - intergenic_variant - - - - - - rs6946611 7:70210753 A 26053 NM_001127231.1 Transcript intron_variant - - - - - - rs6946611 7:70210753 A CCDS47601.1 CCDS47601.1 Transcript intron_variant - - - - - - rs6946611 7:70210753 A CCDS5539.1 CCDS5539.1 Transcript intron_variant - - - - - - rs6946611 7:70210753 A ENSESTG00000006001 ENSESTT00000015201 Transcript intron_variant - - - - - - rs6946611 7:70210753 A 26053 NM_015570.2 Transcript intron_variant - - - - - - rs1525281 7:70473621 G - - - intergenic_variant - - - - - - rs4587229 7:70504393 G - - - intergenic_variant - - - - - - rs1917620 7:70551844 A - - - intergenic_variant - - - - - - rs4717597 7:70923303 G ENSESTG00000026769 ENSESTT00000067612 Transcript intron_variant - - - - - - rs4717597 7:70923303 G CCDS5540.1 CCDS5540.1 Transcript intron_variant - - - - - - rs4717597 7:70923303 G ENSESTG00000026769 ENSESTT00000067596 Transcript intron_variant - - - - - - rs4717597 7:70923303 G ENSESTG00000026769 ENSESTT00000067622 Transcript intron_variant - - - - - - rs4717597 7:70923303 G 64409 NM_022479.1 Transcript intron_variant - - - - - - rs10248381 7:70962271 G ENSESTG00000026769 ENSESTT00000067612 Transcript intron_variant - - - - - - rs10248381 7:70962271 G CCDS5540.1 CCDS5540.1 Transcript intron_variant - - - - - - rs10248381 7:70962271 G ENSESTG00000026769 ENSESTT00000067596 Transcript intron_variant - - - - - - rs10248381 7:70962271 G ENSESTG00000026769 ENSESTT00000067622 Transcript intron_variant - - - - - - rs10248381 7:70962271 G 64409 NM_022479.1 Transcript intron_variant - - - - - - rs4323380 7:70979624 A ENSESTG00000026769 ENSESTT00000067612 Transcript intron_variant - - - - - - rs4323380 7:70979624 A CCDS5540.1 CCDS5540.1 Transcript intron_variant - - - - - - rs4323380 7:70979624 A ENSESTG00000026769 ENSESTT00000067596 Transcript intron_variant - - - - - - rs4323380 7:70979624 A ENSESTG00000026769 ENSESTT00000067622 Transcript intron_variant - - - - - - rs4323380 7:70979624 A 64409 NM_022479.1 Transcript intron_variant - - - - - - rs6460665 7:71004127 G ENSESTG00000026769 ENSESTT00000067612 Transcript intron_variant - - - - - - rs6460665 7:71004127 G CCDS5540.1 CCDS5540.1 Transcript intron_variant - - - - - - rs6460665 7:71004127 G ENSESTG00000026769 ENSESTT00000067596 Transcript intron_variant - - - - - - rs6460665 7:71004127 G ENSESTG00000026769 ENSESTT00000067622 Transcript intron_variant - - - - - - rs6460665 7:71004127 G 64409 NM_022479.1 Transcript intron_variant - - - - - - rs3942005 7:71058200 G ENSESTG00000026769 ENSESTT00000067612 Transcript intron_variant - - - - - - rs3942005 7:71058200 G CCDS5540.1 CCDS5540.1 Transcript intron_variant - - - - - - rs3942005 7:71058200 G ENSESTG00000026769 ENSESTT00000067596 Transcript intron_variant - - - - - - rs3942005 7:71058200 G ENSESTG00000026769 ENSESTT00000067622 Transcript intron_variant - - - - - - rs3942005 7:71058200 G 64409 NM_022479.1 Transcript intron_variant - - - - - - rs645346 7:71167474 T ENSESTG00000026769 ENSESTT00000067612 Transcript intron_variant - - - - - - rs645346 7:71167474 T CCDS5540.1 CCDS5540.1 Transcript intron_variant - - - - - - rs645346 7:71167474 T ENSESTG00000026769 ENSESTT00000067596 Transcript intron_variant - - - - - - rs645346 7:71167474 T ENSESTG00000026769 ENSESTT00000067622 Transcript intron_variant - - - - - - rs645346 7:71167474 T 64409 NM_022479.1 Transcript intron_variant - - - - - - rs654090 7:71181587 A ENSESTG00000026769 ENSESTT00000067612 Transcript downstream_gene_variant - - - - - - DISTANCE=4227 rs654090 7:71181587 A CCDS5540.1 CCDS5540.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4456 rs654090 7:71181587 A ENSESTG00000026769 ENSESTT00000067596 Transcript downstream_gene_variant - - - - - - DISTANCE=4227 rs654090 7:71181587 A ENSESTG00000026769 ENSESTT00000067622 Transcript downstream_gene_variant - - - - - - DISTANCE=4227 rs654090 7:71181587 A 64409 NM_022479.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3003 rs10807739 7:71316317 A 83698 NM_001017440.2 Transcript intron_variant - - - - - - rs10807739 7:71316317 A CCDS47603.1 CCDS47603.1 Transcript intron_variant - - - - - - rs10807739 7:71316317 A CCDS5541.1 CCDS5541.1 Transcript intron_variant - - - - - - rs10807739 7:71316317 A 83698 NM_031468.3 Transcript intron_variant - - - - - - rs2428280 7:71717348 G 83698 NM_001017440.2 Transcript intron_variant - - - - - - rs2428280 7:71717348 G ENSESTG00000026881 ENSESTT00000067747 Transcript intron_variant - - - - - - rs2428280 7:71717348 G CCDS47603.1 CCDS47603.1 Transcript intron_variant - - - - - - rs2428280 7:71717348 G ENSESTG00000026881 ENSESTT00000067759 Transcript intron_variant - - - - - - rs2428280 7:71717348 G CCDS5541.1 CCDS5541.1 Transcript intron_variant - - - - - - rs2428280 7:71717348 G 83698 NM_031468.3 Transcript intron_variant - - - - - - rs2428280 7:71717348 G ENSESTG00000026881 ENSESTT00000067744 Transcript intron_variant - - - - - - rs10265420 7:72313743 C - - - intergenic_variant - - - - - - rs42134 7:72805451 T - - - intergenic_variant - - - - - - rs2030923 7:73172999 G - ENSR00000310759 RegulatoryFeature regulatory_region_variant - - - - - - rs2030923 7:73172999 G - - - intergenic_variant - - - - - - rs6967002 7:73928510 A - ENSR00001560851 RegulatoryFeature regulatory_region_variant - - - - - - rs6967002 7:73928510 A CCDS5571.1 CCDS5571.1 Transcript intron_variant - - - - - - rs6967002 7:73928510 A ENSESTG00000032158 ENSESTT00000081179 Transcript intron_variant - - - - - - rs6967002 7:73928510 A 9569 NM_001199207.1 Transcript intron_variant - - - - - - rs6967002 7:73928510 A CCDS56492.1 CCDS56492.1 Transcript intron_variant - - - - - - rs6967002 7:73928510 A 9569 NM_005685.3 Transcript intron_variant - - - - - - rs6967002 7:73928510 A 9569 NM_016328.2 Transcript intron_variant - - - - - - rs6967002 7:73928510 A ENSESTG00000032158 ENSESTT00000081145 Transcript intron_variant - - - - - - rs6967002 7:73928510 A CCDS47613.1 CCDS47613.1 Transcript intron_variant - - - - - - rs794372 7:75150676 G ENSESTG00000010814 ENSESTT00000027084 Transcript intron_variant - - - - - - rs794372 7:75150676 G 5387 NR_028059.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs794372 7:75150676 G ENSESTG00000010814 ENSESTT00000027088 Transcript intron_variant - - - - - - rs794372 7:75150676 G ENSESTG00000010814 ENSESTT00000027078 Transcript intron_variant - - - - - - rs794354 7:75199023 A CCDS59060.1 CCDS59060.1 Transcript intron_variant - - - - - - rs794354 7:75199023 A CCDS34669.1 CCDS34669.1 Transcript intron_variant - - - - - - rs794354 7:75199023 A ENSESTG00000010739 ENSESTT00000026897 Transcript intron_variant - - - - - - rs794354 7:75199023 A 3092 NM_001243198.1 Transcript intron_variant - - - - - - rs794354 7:75199023 A 3092 NM_005338.5 Transcript intron_variant - - - - - - rs794354 7:75199023 A ENSESTG00000010739 ENSESTT00000026895 Transcript intron_variant - - - - - - rs807873 7:75266201 G CCDS59060.1 CCDS59060.1 Transcript intron_variant - - - - - - rs807873 7:75266201 G CCDS34669.1 CCDS34669.1 Transcript intron_variant - - - - - - rs807873 7:75266201 G 3092 NM_001243198.1 Transcript intron_variant - - - - - - rs807873 7:75266201 G 3092 NM_005338.5 Transcript intron_variant - - - - - - rs807873 7:75266201 G ENSESTG00000010739 ENSESTT00000026895 Transcript intron_variant - - - - - - rs807873 7:75266201 G ENSESTG00000010739 ENSESTT00000026884 Transcript intron_variant - - - - - - rs4732519 7:75621827 G ENSESTG00000011805 ENSESTT00000029640 Transcript downstream_gene_variant - - - - - - DISTANCE=3833 rs4732519 7:75621827 G ENSESTG00000011829 ENSESTT00000029679 Transcript 5_prime_UTR_variant 234 - - - - - rs4732519 7:75621827 G 83862 NM_031925.2 Transcript stop_lost 234 130 44 */Q Tag/Cag - rs4732519 7:75621827 G ENSESTG00000011805 ENSESTT00000029629 Transcript downstream_gene_variant - - - - - - DISTANCE=3833 rs4732519 7:75621827 G CCDS5580.1 CCDS5580.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3959 rs4732519 7:75621827 G 51657 NM_016086.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3828 rs4732519 7:75621827 G ENSESTG00000011805 ENSESTT00000029646 Transcript downstream_gene_variant - - - - - - DISTANCE=3837 rs4732519 7:75621827 G ENSESTG00000011829 ENSESTT00000029681 Transcript 5_prime_UTR_variant 234 - - - - - rs4732557 7:75703166 G - - - intergenic_variant - - - - - - rs38670 7:76387415 T - - - intergenic_variant - - - - - - rs1100234 7:77601721 C - - - intergenic_variant - - - - - - rs6956767 7:77882288 A 9863 NM_012301.3 Transcript intron_variant - - - - - - rs6956767 7:77882288 A CCDS5594.1 CCDS5594.1 Transcript intron_variant - - - - - - rs6956767 7:77882288 A ENSESTG00000012081 ENSESTT00000030242 Transcript downstream_gene_variant - - - - - - DISTANCE=3040 rs979110 7:78125172 T 9863 NM_012301.3 Transcript intron_variant - - - - - - rs979110 7:78125172 T CCDS5594.1 CCDS5594.1 Transcript intron_variant - - - - - - rs540929 7:78471270 C 9863 NM_012301.3 Transcript intron_variant - - - - - - rs540929 7:78471270 C CCDS5594.1 CCDS5594.1 Transcript intron_variant - - - - - - rs491282 7:78472759 T 9863 NM_012301.3 Transcript intron_variant - - - - - - rs491282 7:78472759 T CCDS5594.1 CCDS5594.1 Transcript intron_variant - - - - - - rs848935 7:78981512 C 9863 NM_012301.3 Transcript intron_variant - - - - - - rs848935 7:78981512 C CCDS5594.1 CCDS5594.1 Transcript intron_variant - - - - - - rs28690914 7:79038710 C 9863 NM_012301.3 Transcript intron_variant - - - - - - rs28690914 7:79038710 C CCDS5594.1 CCDS5594.1 Transcript intron_variant - - - - - - rs4535673 7:79195951 C - - - intergenic_variant - - - - - - rs2525811 7:79474259 C - - - intergenic_variant - - - - - - rs6467044 7:79822444 A 2770 NM_001256414.1 Transcript intron_variant - - - - - - rs6467044 7:79822444 A CCDS59061.1 CCDS59061.1 Transcript intron_variant - - - - - - rs6467044 7:79822444 A CCDS5595.1 CCDS5595.1 Transcript intron_variant - - - - - - rs6467044 7:79822444 A ENSESTG00000001800 ENSESTT00000004447 Transcript intron_variant - - - - - - rs6467044 7:79822444 A 2770 NM_002069.5 Transcript intron_variant - - - - - - rs6467044 7:79822444 A ENSESTG00000001800 ENSESTT00000004450 Transcript intron_variant - - - - - - rs6467044 7:79822444 A ENSESTG00000001800 ENSESTT00000004427 Transcript downstream_gene_variant - - - - - - DISTANCE=4001 rs306698 7:79885698 C - - - intergenic_variant - - - - - - rs306719 7:79901318 T - - - intergenic_variant - - - - - - rs306695 7:79904564 G - ENSR00000629182 RegulatoryFeature regulatory_region_variant - - - - - - rs306695 7:79904564 G - - - intergenic_variant - - - - - - rs6945227 7:80136233 C 346562 NM_001102386.1 Transcript intron_variant - - - - - - rs6945227 7:80136233 C CCDS47625.1 CCDS47625.1 Transcript intron_variant - - - - - - rs2204356 7:80189738 C - - - intergenic_variant - - - - - - rs975265 7:81111583 G - - - intergenic_variant - - - - - - rs1029565 7:81292993 C - - - intergenic_variant - - - - - - rs6979555 7:82055151 G 781 NM_000722.2 Transcript intron_variant - - - - - - rs6979555 7:82055151 G CCDS5598.1 CCDS5598.1 Transcript intron_variant - - - - - - rs2709874 7:82914803 A - - - intergenic_variant - - - - - - rs6467942 7:82961815 G - - - intergenic_variant - - - - - - rs42020 7:83245172 G ENSESTG00000017281 ENSESTT00000043515 Transcript intron_variant - - - - - - rs42020 7:83245172 G 9723 NM_012431.2 Transcript intron_variant - - - - - - rs42020 7:83245172 G ENSESTG00000017281 ENSESTT00000043512 Transcript intron_variant - - - - - - rs42020 7:83245172 G CCDS34674.1 CCDS34674.1 Transcript intron_variant - - - - - - rs42020 7:83245172 G 9723 NM_001178129.1 Transcript intron_variant - - - - - - rs118760 7:83277015 A 9723 NM_012431.2 Transcript intron_variant - - - - - - rs118760 7:83277015 A ENSESTG00000017281 ENSESTT00000043512 Transcript intron_variant - - - - - - rs118760 7:83277015 A CCDS34674.1 CCDS34674.1 Transcript intron_variant - - - - - - rs545548 7:83307017 G - ENSR00001561429 RegulatoryFeature regulatory_region_variant - - - - - - rs545548 7:83307017 G - - - intergenic_variant - - - - - - rs302131 7:83327032 T - - - intergenic_variant - - - - - - rs6965146 7:83839550 G - - - intergenic_variant - - - - - - rs7811994 7:85153396 A - - - intergenic_variant - - - - - - rs2055757 7:85395595 T - - - intergenic_variant - - - - - - rs4461823 7:85526318 C - - - intergenic_variant - - - - - - rs2952714 7:85936409 G - - - intergenic_variant - - - - - - rs2536248 7:85959834 C - - - intergenic_variant - - - - - - rs6465065 7:86015666 T - - - intergenic_variant - - - - - - rs781003 7:86220004 C - - - intergenic_variant - - - - - - rs4329208 7:86449260 G ENSESTG00000032672 ENSESTT00000082602 Transcript intron_variant - - - - - - rs4329208 7:86449260 G ENSESTG00000032672 ENSESTT00000082603 Transcript intron_variant - - - - - - rs4329208 7:86449260 G ENSESTG00000032672 ENSESTT00000082595 Transcript intron_variant - - - - - - rs4329208 7:86449260 G ENSESTG00000032672 ENSESTT00000082591 Transcript intron_variant - - - - - - rs4329208 7:86449260 G CCDS5600.1 CCDS5600.1 Transcript intron_variant - - - - - - rs4329208 7:86449260 G ENSESTG00000032672 ENSESTT00000082623 Transcript intron_variant - - - - - - rs4329208 7:86449260 G 2913 NM_000840.2 Transcript intron_variant - - - - - - rs39909 7:87050656 C ENSESTG00000025118 ENSESTT00000063497 Transcript intron_variant - - - - - - rs39909 7:87050656 C CCDS5606.1 CCDS5606.1 Transcript intron_variant - - - - - - rs39909 7:87050656 C 5244 NM_000443.3 Transcript intron_variant - - - - - - rs39909 7:87050656 C 5244 NM_018850.2 Transcript intron_variant - - - - - - rs39909 7:87050656 C CCDS5605.1 CCDS5605.1 Transcript intron_variant - - - - - - rs39909 7:87050656 C ENSESTG00000025206 ENSESTT00000063593 Transcript downstream_gene_variant - - - - - - DISTANCE=2567 rs39909 7:87050656 C CCDS5607.1 CCDS5607.1 Transcript intron_variant - - - - - - rs39909 7:87050656 C ENSESTG00000025118 ENSESTT00000063510 Transcript intron_variant - - - - - - rs39909 7:87050656 C 5244 NM_018849.2 Transcript intron_variant - - - - - - rs239998 7:87951163 C - - - intergenic_variant - - - - - - rs2718341 7:88317513 T - - - intergenic_variant - - - - - - rs2538886 7:88317541 T - - - intergenic_variant - - - - - - rs10952948 7:88709799 G 219578 NM_181646.2 Transcript intron_variant - - - - - - rs10952948 7:88709799 G CCDS5613.1 CCDS5613.1 Transcript intron_variant - - - - - - rs2214053 7:89139135 C ENSESTG00000033325 ENSESTT00000084164 Transcript intron_variant - - - - - - rs2188417 7:89144913 T ENSESTG00000033325 ENSESTT00000084164 Transcript intron_variant - - - - - - rs466 7:89284229 G - - - intergenic_variant - - - - - - rs10275490 7:89514129 C - - - intergenic_variant - - - - - - rs10249756 7:89524008 T - - - intergenic_variant - - - - - - rs6465216 7:89550290 C - - - intergenic_variant - - - - - - rs2374080 7:89585066 C - - - intergenic_variant - - - - - - rs6950422 7:89601366 C - - - intergenic_variant - - - - - - rs12704502 7:89602686 G - - - intergenic_variant - - - - - - rs259148 7:89625421 C - - - intergenic_variant - - - - - - rs1558033 7:89662803 C - - - intergenic_variant - - - - - - rs194532 7:89869119 T 261729 NM_152999.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2127 rs194532 7:89869119 T 261729 NM_001244944.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2127 rs194532 7:89869119 T 261729 NM_001040665.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2127 rs194532 7:89869119 T CCDS43612.1 CCDS43612.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2883 rs194532 7:89869119 T 261729 NM_001040666.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2127 rs194532 7:89869119 T 261729 NM_001244946.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2127 rs194532 7:89869119 T 261729 NM_001244945.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2127 rs194532 7:89869119 T CCDS59064.1 CCDS59064.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2840 rs10249895 7:90119483 G ENSESTG00000030089 ENSESTT00000075749 Transcript intron_variant - - - - - - rs10249895 7:90119483 G ENSESTG00000030089 ENSESTT00000075875 Transcript intron_variant - - - - - - rs10249895 7:90119483 G 100996527 XM_003846241.1 Transcript intron_variant - - - - - - rs10249895 7:90119483 G ENSESTG00000030089 ENSESTT00000075886 Transcript intron_variant - - - - - - rs6954587 7:90182926 C ENSESTG00000030089 ENSESTT00000075749 Transcript intron_variant - - - - - - rs697401 7:90728749 T CCDS5619.1 CCDS5619.1 Transcript intron_variant - - - - - - rs697401 7:90728749 T ENSESTG00000002656 ENSESTT00000006634 Transcript intron_variant - - - - - - rs697401 7:90728749 T 5218 NM_012395.2 Transcript intron_variant - - - - - - rs697401 7:90728749 T ENSESTG00000030089 ENSESTT00000076038 Transcript intron_variant - - - - - - rs697401 7:90728749 T ENSESTG00000030089 ENSESTT00000075999 Transcript intron_variant - - - - - - rs984843 7:91236997 A - - - intergenic_variant - - - - - - rs7791724 7:91275657 G ENSESTG00000002735 ENSESTT00000006784 Transcript upstream_gene_variant - - - - - - DISTANCE=2830 rs6465346 7:91649387 T 10142 NM_147185.2 Transcript intron_variant - - - - - - rs6465346 7:91649387 T CCDS5622.1 CCDS5622.1 Transcript intron_variant - - - - - - rs6465346 7:91649387 T 10142 NM_005751.4 Transcript intron_variant - - - - - - rs6465346 7:91649387 T ENSESTG00000013218 ENSESTT00000033150 Transcript downstream_gene_variant - - - - - - DISTANCE=2975 rs973472 7:91825908 T 889 NM_001013406.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2375 rs973472 7:91825908 T ENSESTG00000013636 ENSESTT00000034170 Transcript downstream_gene_variant - - - - - - DISTANCE=3942 rs973472 7:91825908 T 889 NM_194454.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2375 rs973472 7:91825908 T ENSESTG00000013636 ENSESTT00000034191 Transcript downstream_gene_variant - - - - - - DISTANCE=3942 rs973472 7:91825908 T ENSESTG00000013636 ENSESTT00000034196 Transcript downstream_gene_variant - - - - - - DISTANCE=3942 rs973472 7:91825908 T ENSESTG00000013636 ENSESTT00000034176 Transcript downstream_gene_variant - - - - - - DISTANCE=3942 rs973472 7:91825908 T CCDS34679.1 CCDS34679.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4142 rs973472 7:91825908 T 889 NM_194456.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2375 rs973472 7:91825908 T 889 NM_194455.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2375 rs973472 7:91825908 T ENSESTG00000013636 ENSESTT00000034173 Transcript downstream_gene_variant - - - - - - DISTANCE=3942 rs973472 7:91825908 T CCDS5624.1 CCDS5624.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4142 rs973472 7:91825908 T ENSESTG00000013636 ENSESTT00000034186 Transcript downstream_gene_variant - - - - - - DISTANCE=3942 rs973472 7:91825908 T 889 NM_004912.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2375 rs973472 7:91825908 T ENSESTG00000013636 ENSESTT00000034179 Transcript downstream_gene_variant - - - - - - DISTANCE=3942 rs7785589 7:91959646 G ENSESTG00000013288 ENSESTT00000033335 Transcript downstream_gene_variant - - - - - - DISTANCE=2432 rs7785589 7:91959646 G ENSESTG00000013288 ENSESTT00000033387 Transcript intron_variant - - - - - - rs7785589 7:91959646 G CCDS47639.1 CCDS47639.1 Transcript intron_variant - - - - - - rs7785589 7:91959646 G ENSESTG00000013288 ENSESTT00000033383 Transcript intron_variant - - - - - - rs7785589 7:91959646 G 54467 NM_019004.1 Transcript intron_variant - - - - - - rs7785589 7:91959646 G ENSESTG00000013288 ENSESTT00000033377 Transcript intron_variant - - - - - - rs4729029 7:91984220 G ENSESTG00000013288 ENSESTT00000033387 Transcript intron_variant - - - - - - rs4729029 7:91984220 G CCDS47639.1 CCDS47639.1 Transcript intron_variant - - - - - - rs4729029 7:91984220 G ENSESTG00000013288 ENSESTT00000033383 Transcript intron_variant - - - - - - rs4729029 7:91984220 G ENSESTG00000013288 ENSESTT00000033395 Transcript intron_variant - - - - - - rs4729029 7:91984220 G 54467 NM_019004.1 Transcript intron_variant - - - - - - rs4729029 7:91984220 G ENSESTG00000013288 ENSESTT00000033377 Transcript intron_variant - - - - - - rs4729029 7:91984220 G ENSESTG00000013288 ENSESTT00000033394 Transcript intron_variant - - - - - - rs7791014 7:91988403 G ENSESTG00000013288 ENSESTT00000033387 Transcript intron_variant - - - - - - rs7791014 7:91988403 G CCDS47639.1 CCDS47639.1 Transcript intron_variant - - - - - - rs7791014 7:91988403 G ENSESTG00000013288 ENSESTT00000033383 Transcript intron_variant - - - - - - rs7791014 7:91988403 G ENSESTG00000013288 ENSESTT00000033395 Transcript intron_variant - - - - - - rs7791014 7:91988403 G 54467 NM_019004.1 Transcript intron_variant - - - - - - rs7791014 7:91988403 G ENSESTG00000013288 ENSESTT00000033377 Transcript intron_variant - - - - - - rs7791014 7:91988403 G ENSESTG00000013288 ENSESTT00000033394 Transcript intron_variant - - - - - - rs38804 7:92071302 T - ENSR00001561829 RegulatoryFeature regulatory_region_variant - - - - - - rs38804 7:92071302 T - - - intergenic_variant - - - - - - rs972923 7:92119284 G - ENSR00001561832 RegulatoryFeature regulatory_region_variant - - - - - - rs972923 7:92119284 G ENSESTG00000013597 ENSESTT00000034061 Transcript downstream_gene_variant - - - - - - DISTANCE=4154 rs972923 7:92119284 G ENSESTG00000013386 ENSESTT00000033534 Transcript upstream_gene_variant - - - - - - DISTANCE=115 rs972923 7:92119284 G CCDS5627.1 CCDS5627.1 Transcript intron_variant - - - - - - rs972923 7:92119284 G 5189 NM_000466.2 Transcript intron_variant - - - - - - rs10246926 7:92475304 C ENSESTG00000013435 ENSESTT00000033628 Transcript intron_variant - - - - - - rs10246926 7:92475304 C ENSESTG00000013435 ENSESTT00000033626 Transcript intron_variant - - - - - - rs6465370 7:92664042 G - - - intergenic_variant - - - - - - rs42509 7:92819058 A ENSESTG00000030298 ENSESTT00000076248 Transcript downstream_gene_variant - - - - - - DISTANCE=2509 rs42509 7:92819058 A CCDS43616.1 CCDS43616.1 Transcript intron_variant - - - - - - rs42509 7:92819058 A ENSESTG00000030298 ENSESTT00000076231 Transcript intron_variant - - - - - - rs42509 7:92819058 A 253012 NM_001039372.1 Transcript intron_variant - - - - - - rs42509 7:92819058 A CCDS5629.1 CCDS5629.1 Transcript intron_variant - - - - - - rs42509 7:92819058 A 253012 NM_198151.1 Transcript intron_variant - - - - - - rs1533833 7:94275412 C ENSESTG00000016230 ENSESTT00000040795 Transcript intron_variant - - - - - - rs1533833 7:94275412 C ENSESTG00000016230 ENSESTT00000040779 Transcript intron_variant - - - - - - rs1533833 7:94275412 C 8910 NM_001099400.1 Transcript intron_variant - - - - - - rs1533833 7:94275412 C CCDS47643.1 CCDS47643.1 Transcript intron_variant - - - - - - rs1533833 7:94275412 C CCDS5637.1 CCDS5637.1 Transcript intron_variant - - - - - - rs1533833 7:94275412 C ENSESTG00000016230 ENSESTT00000040804 Transcript intron_variant - - - - - - rs1533833 7:94275412 C 8910 NM_001099401.1 Transcript intron_variant - - - - - - rs1533833 7:94275412 C 8910 NM_003919.2 Transcript intron_variant - - - - - - rs1533833 7:94275412 C CCDS47642.1 CCDS47642.1 Transcript intron_variant - - - - - - rs1522546 7:94280436 T ENSESTG00000016230 ENSESTT00000040795 Transcript intron_variant - - - - - - rs1522546 7:94280436 T ENSESTG00000016230 ENSESTT00000040779 Transcript intron_variant - - - - - - rs1522546 7:94280436 T 8910 NM_001099400.1 Transcript intron_variant - - - - - - rs1522546 7:94280436 T CCDS47643.1 CCDS47643.1 Transcript intron_variant - - - - - - rs1522546 7:94280436 T CCDS5637.1 CCDS5637.1 Transcript intron_variant - - - - - - rs1522546 7:94280436 T ENSESTG00000016230 ENSESTT00000040804 Transcript intron_variant - - - - - - rs1522546 7:94280436 T 8910 NM_001099401.1 Transcript intron_variant - - - - - - rs1522546 7:94280436 T 8910 NM_003919.2 Transcript intron_variant - - - - - - rs1522546 7:94280436 T CCDS47642.1 CCDS47642.1 Transcript intron_variant - - - - - - rs9648900 7:94883781 C CCDS34683.1 CCDS34683.1 Transcript intron_variant - - - - - - rs9648900 7:94883781 C CCDS55129.1 CCDS55129.1 Transcript intron_variant - - - - - - rs9648900 7:94883781 C CCDS55128.1 CCDS55128.1 Transcript intron_variant - - - - - - rs9648900 7:94883781 C ENSESTG00000020531 ENSESTT00000051505 Transcript intron_variant - - - - - - rs9648900 7:94883781 C ENSESTG00000020531 ENSESTT00000051535 Transcript intron_variant - - - - - - rs9648900 7:94883781 C CCDS55127.1 CCDS55127.1 Transcript intron_variant - - - - - - rs9648900 7:94883781 C ENSESTG00000020531 ENSESTT00000051524 Transcript intron_variant - - - - - - rs9648900 7:94883781 C 55607 NM_001166163.1 Transcript intron_variant - - - - - - rs9648900 7:94883781 C 55607 NM_017650.2 Transcript intron_variant - - - - - - rs9648900 7:94883781 C 55607 NM_001166161.1 Transcript intron_variant - - - - - - rs9648900 7:94883781 C 55607 NM_001166160.1 Transcript intron_variant - - - - - - rs9648900 7:94883781 C 55607 NM_001166162.1 Transcript intron_variant - - - - - - rs1227493 7:95333619 G - - - intergenic_variant - - - - - - rs7800612 7:95752908 C ENSESTG00000002922 ENSESTT00000007381 Transcript intron_variant - - - - - - rs7800612 7:95752908 C CCDS55130.1 CCDS55130.1 Transcript intron_variant - - - - - - rs7800612 7:95752908 C ENSESTG00000002922 ENSESTT00000007388 Transcript intron_variant - - - - - - rs7800612 7:95752908 C ENSESTG00000002922 ENSESTT00000007359 Transcript intron_variant - - - - - - rs7800612 7:95752908 C 10165 NM_014251.2 Transcript intron_variant - - - - - - rs7800612 7:95752908 C CCDS5645.1 CCDS5645.1 Transcript intron_variant - - - - - - rs7800612 7:95752908 C 10165 NR_027662.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7800612 7:95752908 C 10165 NM_001160210.1 Transcript intron_variant - - - - - - rs7800612 7:95752908 C ENSESTG00000002922 ENSESTT00000007379 Transcript intron_variant - - - - - - rs4574776 7:95902566 A CCDS55130.1 CCDS55130.1 Transcript intron_variant - - - - - - rs4574776 7:95902566 A ENSESTG00000002922 ENSESTT00000007359 Transcript intron_variant - - - - - - rs4574776 7:95902566 A ENSESTG00000002922 ENSESTT00000007372 Transcript intron_variant - - - - - - rs4574776 7:95902566 A 10165 NM_014251.2 Transcript intron_variant - - - - - - rs4574776 7:95902566 A CCDS5645.1 CCDS5645.1 Transcript intron_variant - - - - - - rs4574776 7:95902566 A 10165 NR_027662.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4574776 7:95902566 A 10165 NM_001160210.1 Transcript intron_variant - - - - - - rs4574776 7:95902566 A ENSESTG00000002922 ENSESTT00000007374 Transcript intron_variant - - - - - - rs2524964 7:95959152 G - - - intergenic_variant - - - - - - rs4990848 7:96195717 T ENSESTG00000002892 ENSESTT00000007226 Transcript intron_variant - - - - - - rs4727342 7:96310722 C ENSESTG00000002892 ENSESTT00000007226 Transcript intron_variant - - - - - - rs4727342 7:96310722 C ENSESTG00000002892 ENSESTT00000007199 Transcript intron_variant - - - - - - rs4727342 7:96310722 C ENSESTG00000002892 ENSESTT00000007195 Transcript intron_variant - - - - - - rs10279804 7:96403542 A - - - intergenic_variant - - - - - - rs1207685 7:96556779 C - - - intergenic_variant - - - - - - rs1362372 7:96969682 T - - - intergenic_variant - - - - - - rs1799064 7:97629931 G - ENSR00001562138 RegulatoryFeature regulatory_region_variant - - - - - - rs1799064 7:97629931 G - PL0014.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_NAME=Jaspar_Matrix_mxl-1::mdl-1:PL0014.1;HIGH_INF_POS=N rs1799064 7:97629931 G - PB0043.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_NAME=Jaspar_Matrix_Max:PB0043.1;HIGH_INF_POS=N rs1799064 7:97629931 G - PL0014.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_NAME=Jaspar_Matrix_mxl-1::mdl-1:PL0014.1;HIGH_INF_POS=N rs1799064 7:97629931 G - - - intergenic_variant - - - - - - rs6970140 7:97778780 G CCDS5654.1 CCDS5654.1 Transcript intron_variant - - - - - - rs6970140 7:97778780 G ENSESTG00000034495 ENSESTT00000087269 Transcript intron_variant - - - - - - rs6970140 7:97778780 G ENSESTG00000034495 ENSESTT00000087266 Transcript intron_variant - - - - - - rs6970140 7:97778780 G 22853 NM_014916.3 Transcript intron_variant - - - - - - rs6970140 7:97778780 G ENSESTG00000034495 ENSESTT00000087272 Transcript intron_variant - - - - - - rs4729416 7:97851109 C ENSESTG00000034642 ENSESTT00000087588 Transcript downstream_gene_variant - - - - - - DISTANCE=1259 rs4729416 7:97851109 C CCDS47648.1 CCDS47648.1 Transcript intron_variant - - - - - - rs4729416 7:97851109 C 25851 NM_015395.1 Transcript intron_variant - - - - - - rs1635610 7:97952506 C ENSESTG00000034583 ENSESTT00000087538 Transcript intron_variant - - - - - - rs1635610 7:97952506 C ENSESTG00000034583 ENSESTT00000087529 Transcript intron_variant - - - - - - rs1635610 7:97952506 C ENSESTG00000034583 ENSESTT00000087535 Transcript intron_variant - - - - - - rs1635610 7:97952506 C CCDS34687.1 CCDS34687.1 Transcript intron_variant - - - - - - rs1635610 7:97952506 C ENSESTG00000034583 ENSESTT00000087526 Transcript intron_variant - - - - - - rs1635610 7:97952506 C 55971 NM_018842.4 Transcript intron_variant - - - - - - rs1635610 7:97952506 C ENSESTG00000034583 ENSESTT00000087545 Transcript intron_variant - - - - - - rs10755865 7:97971021 C ENSESTG00000034583 ENSESTT00000087538 Transcript intron_variant - - - - - - rs10755865 7:97971021 C ENSESTG00000034583 ENSESTT00000087529 Transcript intron_variant - - - - - - rs10755865 7:97971021 C ENSESTG00000034583 ENSESTT00000087535 Transcript intron_variant - - - - - - rs10755865 7:97971021 C CCDS34687.1 CCDS34687.1 Transcript intron_variant - - - - - - rs10755865 7:97971021 C ENSESTG00000034583 ENSESTT00000087526 Transcript intron_variant - - - - - - rs10755865 7:97971021 C 55971 NM_018842.4 Transcript intron_variant - - - - - - rs10755865 7:97971021 C ENSESTG00000034583 ENSESTT00000087545 Transcript intron_variant - - - - - - rs1622102 7:97981419 C ENSESTG00000034583 ENSESTT00000087538 Transcript intron_variant - - - - - - rs1622102 7:97981419 C ENSESTG00000034583 ENSESTT00000087529 Transcript intron_variant - - - - - - rs1622102 7:97981419 C ENSESTG00000034583 ENSESTT00000087535 Transcript intron_variant - - - - - - rs1622102 7:97981419 C CCDS34687.1 CCDS34687.1 Transcript intron_variant - - - - - - rs1622102 7:97981419 C ENSESTG00000034583 ENSESTT00000087526 Transcript intron_variant - - - - - - rs1622102 7:97981419 C 55971 NM_018842.4 Transcript intron_variant - - - - - - rs1622102 7:97981419 C ENSESTG00000034583 ENSESTT00000087545 Transcript intron_variant - - - - - - rs4727393 7:98032246 C ENSESTG00000034583 ENSESTT00000087538 Transcript upstream_gene_variant - - - - - - DISTANCE=2641 rs4727393 7:98032246 C ENSESTG00000034583 ENSESTT00000087529 Transcript upstream_gene_variant - - - - - - DISTANCE=1860 rs4727393 7:98032246 C ENSESTG00000034583 ENSESTT00000087535 Transcript upstream_gene_variant - - - - - - DISTANCE=2641 rs4727393 7:98032246 C CCDS34687.1 CCDS34687.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2082 rs4727393 7:98032246 C ENSESTG00000034583 ENSESTT00000087526 Transcript upstream_gene_variant - - - - - - DISTANCE=1860 rs4727393 7:98032246 C 55971 NM_018842.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1819 rs6974980 7:98424140 A - - - intergenic_variant - - - - - - rs6465725 7:98436604 C - - - intergenic_variant - - - - - - rs1565047 7:98437952 G - - - intergenic_variant - - - - - - rs7812000 7:98438907 C - - - intergenic_variant - - - - - - rs7790762 7:98674370 T - ENSR00000682831 RegulatoryFeature regulatory_region_variant - - - - - - rs7790762 7:98674370 T ENSESTG00000009656 ENSESTT00000024193 Transcript intron_variant - - - - - - rs7790762 7:98674370 T 57154 NM_020429.2 Transcript intron_variant - - - - - - rs7790762 7:98674370 T 57154 NM_181349.2 Transcript intron_variant - - - - - - rs7790762 7:98674370 T CCDS34689.1 CCDS34689.1 Transcript intron_variant - - - - - - rs7790762 7:98674370 T 57154 NM_001199847.1 Transcript intron_variant - - - - - - rs7790762 7:98674370 T ENSESTG00000009656 ENSESTT00000024206 Transcript intron_variant - - - - - - rs7790762 7:98674370 T CCDS34690.1 CCDS34690.1 Transcript intron_variant - - - - - - rs6465736 7:98701044 G - ENSR00001050150 RegulatoryFeature regulatory_region_variant - - - - - - rs6465736 7:98701044 G ENSESTG00000009656 ENSESTT00000024193 Transcript intron_variant - - - - - - rs6465736 7:98701044 G 57154 NM_020429.2 Transcript intron_variant - - - - - - rs6465736 7:98701044 G 57154 NM_181349.2 Transcript intron_variant - - - - - - rs6465736 7:98701044 G CCDS34689.1 CCDS34689.1 Transcript intron_variant - - - - - - rs6465736 7:98701044 G 57154 NM_001199847.1 Transcript intron_variant - - - - - - rs6465736 7:98701044 G ENSESTG00000009656 ENSESTT00000024206 Transcript intron_variant - - - - - - rs6465736 7:98701044 G CCDS34690.1 CCDS34690.1 Transcript intron_variant - - - - - - rs6972972 7:98760180 G - ENSR00000630943 RegulatoryFeature regulatory_region_variant - - - - - - rs6972972 7:98760180 G - - - intergenic_variant - - - - - - rs2527905 7:99522568 A ENSESTG00000022085 ENSESTT00000055622 Transcript upstream_gene_variant - - - - - - DISTANCE=4447 rs2527905 7:99522568 A CCDS34697.1 CCDS34697.1 Transcript intron_variant - - - - - - rs2527905 7:99522568 A 349149 NM_181538.2 Transcript intron_variant - - - - - - rs10239266 7:100342950 C - ENSR00000631211 RegulatoryFeature regulatory_region_variant - - - - - - rs10239266 7:100342950 C 7455 NM_173059.1 Transcript intron_variant - - - - - - rs10239266 7:100342950 C 7455 NM_003386.1 Transcript intron_variant - - - - - - rs6465821 7:101226589 G - - - intergenic_variant - - - - - - rs2970468 7:101476316 C 1523 NM_001913.3 Transcript intron_variant - - - - - - rs2970468 7:101476316 C CCDS56498.1 CCDS56498.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C 1523 NM_001202546.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C CCDS56500.1 CCDS56500.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C 1523 NM_181552.3 Transcript intron_variant - - - - - - rs2970468 7:101476316 C 1523 NM_181500.2 Transcript intron_variant - - - - - - rs2970468 7:101476316 C ENSESTG00000032874 ENSESTT00000083303 Transcript intron_variant - - - - - - rs2970468 7:101476316 C 1523 NM_001202545.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C CCDS5720.1 CCDS5720.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C CCDS59071.1 CCDS59071.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C ENSESTG00000032874 ENSESTT00000083297 Transcript intron_variant - - - - - - rs2970468 7:101476316 C CCDS47672.1 CCDS47672.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C CCDS5721.1 CCDS5721.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C ENSESTG00000032874 ENSESTT00000083077 Transcript intron_variant - - - - - - rs2970468 7:101476316 C 1523 NM_001202544.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C CCDS56499.1 CCDS56499.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C 1523 NM_001202543.1 Transcript intron_variant - - - - - - rs2970468 7:101476316 C ENSESTG00000032874 ENSESTT00000083321 Transcript intron_variant - - - - - - rs448877 7:101671585 G 1523 NM_001913.3 Transcript intron_variant - - - - - - rs448877 7:101671585 G CCDS56498.1 CCDS56498.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083354 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083359 Transcript intron_variant - - - - - - rs448877 7:101671585 G 1523 NM_001202546.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083391 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083344 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083330 Transcript intron_variant - - - - - - rs448877 7:101671585 G CCDS56500.1 CCDS56500.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G 1523 NM_181552.3 Transcript intron_variant - - - - - - rs448877 7:101671585 G 1523 NM_181500.2 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083303 Transcript intron_variant - - - - - - rs448877 7:101671585 G 1523 NM_001202545.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083373 Transcript intron_variant - - - - - - rs448877 7:101671585 G CCDS59071.1 CCDS59071.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G CCDS5720.1 CCDS5720.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G CCDS47672.1 CCDS47672.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083297 Transcript intron_variant - - - - - - rs448877 7:101671585 G CCDS5721.1 CCDS5721.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083364 Transcript intron_variant - - - - - - rs448877 7:101671585 G 1523 NM_001202544.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G CCDS56499.1 CCDS56499.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083380 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083337 Transcript intron_variant - - - - - - rs448877 7:101671585 G 1523 NM_001202543.1 Transcript intron_variant - - - - - - rs448877 7:101671585 G ENSESTG00000032874 ENSESTT00000083321 Transcript intron_variant - - - - - - rs803086 7:101921522 G 1523 NM_001913.3 Transcript intron_variant - - - - - - rs803086 7:101921522 G ENSESTG00000032874 ENSESTT00000083354 Transcript intron_variant - - - - - - rs803086 7:101921522 G 1523 NM_001202546.1 Transcript intron_variant - - - - - - rs803086 7:101921522 G ENSESTG00000032874 ENSESTT00000083330 Transcript intron_variant - - - - - - rs803086 7:101921522 G ENSESTG00000032874 ENSESTT00000083482 Transcript intron_variant - - - - - - rs803086 7:101921522 G CCDS56500.1 CCDS56500.1 Transcript intron_variant - - - - - - rs803086 7:101921522 G ENSESTG00000032874 ENSESTT00000083402 Transcript downstream_gene_variant - - - - - - DISTANCE=197 rs803086 7:101921522 G 1523 NM_181500.2 Transcript intron_variant - - - - - - rs803086 7:101921522 G ENSESTG00000032874 ENSESTT00000083459 Transcript intron_variant - - - - - - rs803086 7:101921522 G 1523 NM_001202545.1 Transcript intron_variant - - - - - - rs803086 7:101921522 G ENSESTG00000032874 ENSESTT00000083373 Transcript intron_variant - - - - - - rs803086 7:101921522 G CCDS5720.1 CCDS5720.1 Transcript intron_variant - - - - - - rs803086 7:101921522 G CCDS59071.1 CCDS59071.1 Transcript intron_variant - - - - - - rs803086 7:101921522 G ENSESTG00000032874 ENSESTT00000083297 Transcript intron_variant - - - - - - rs803086 7:101921522 G CCDS47672.1 CCDS47672.1 Transcript intron_variant - - - - - - rs803086 7:101921522 G 1523 NM_001202544.1 Transcript intron_variant - - - - - - rs803086 7:101921522 G CCDS56499.1 CCDS56499.1 Transcript intron_variant - - - - - - rs711443 7:103557697 G CCDS34722.1 CCDS34722.1 Transcript intron_variant - - - - - - rs711443 7:103557697 G 5649 NM_173054.2 Transcript intron_variant - - - - - - rs711443 7:103557697 G 5649 NM_005045.3 Transcript intron_variant - - - - - - rs711443 7:103557697 G CCDS47680.1 CCDS47680.1 Transcript intron_variant - - - - - - rs2385236 7:104028983 A 375612 NM_199000.2 Transcript intron_variant - - - - - - rs1073013 7:104263140 G 375612 NM_199000.2 Transcript intron_variant - - - - - - rs916706 7:104592936 A ENSESTG00000010273 ENSESTT00000025690 Transcript intron_variant - - - - - - rs916706 7:104592936 A ENSESTG00000010273 ENSESTT00000025694 Transcript intron_variant - - - - - - rs886786 7:104781894 A - ENSR00000068281 RegulatoryFeature regulatory_region_variant - - - - - - rs886786 7:104781894 A CCDS5735.1 CCDS5735.1 Transcript intron_variant - - - - - - rs886786 7:104781894 A CCDS34724.1 CCDS34724.1 Transcript intron_variant - - - - - - rs886786 7:104781894 A ENSESTG00000010404 ENSESTT00000026101 Transcript intron_variant - - - - - - rs886786 7:104781894 A 6733 NM_182691.1 Transcript intron_variant - - - - - - rs886786 7:104781894 A 6733 NM_182692.1 Transcript intron_variant - - - - - - rs1204065 7:104971962 A CCDS34724.1 CCDS34724.1 Transcript intron_variant - - - - - - rs1204065 7:104971962 A ENSESTG00000010404 ENSESTT00000026046 Transcript intron_variant - - - - - - rs1204065 7:104971962 A 6733 NM_182692.1 Transcript intron_variant - - - - - - rs1706894 7:105242742 T 222255 NM_020725.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2479 rs1706894 7:105242742 T 222255 NM_138495.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2479 rs1204368 7:105426756 T ENSESTG00000010376 ENSESTT00000025972 Transcript intron_variant - - - - - - rs1204368 7:105426756 T ENSESTG00000010376 ENSESTT00000025985 Transcript intron_variant - - - - - - rs1204368 7:105426756 T 222255 NM_152749.3 Transcript intron_variant - - - - - - rs1204368 7:105426756 T ENSESTG00000010376 ENSESTT00000025968 Transcript intron_variant - - - - - - rs1204368 7:105426756 T ENSESTG00000010376 ENSESTT00000025979 Transcript intron_variant - - - - - - rs1204368 7:105426756 T ENSESTG00000010376 ENSESTT00000025951 Transcript downstream_gene_variant - - - - - - DISTANCE=2083 rs1204368 7:105426756 T CCDS34727.1 CCDS34727.1 Transcript intron_variant - - - - - - rs1204368 7:105426756 T CCDS47682.1 CCDS47682.1 Transcript intron_variant - - - - - - rs1204368 7:105426756 T 222255 NM_020725.1 Transcript intron_variant - - - - - - rs176515 7:105789199 T - - - intergenic_variant - - - - - - rs12705364 7:105875656 C - - - intergenic_variant - - - - - - rs179895 7:106035564 T - - - intergenic_variant - - - - - - rs179897 7:106036872 C - - - intergenic_variant - - - - - - rs2704986 7:106051668 T - - - intergenic_variant - - - - - - rs7809190 7:106197514 T - - - intergenic_variant - - - - - - rs41840 7:106267680 G - - - intergenic_variant - - - - - - rs4730216 7:106646452 A - - - intergenic_variant - - - - - - rs11770477 7:106653139 G - - - intergenic_variant - - - - - - rs257383 7:106804627 T 26959 NM_012257.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4833 rs257383 7:106804627 T ENSESTG00000018412 ENSESTT00000046487 Transcript downstream_gene_variant - - - - - - DISTANCE=4230 rs257383 7:106804627 T ENSESTG00000018499 ENSESTT00000046722 Transcript upstream_gene_variant - - - - - - DISTANCE=4834 rs257383 7:106804627 T ENSESTG00000018412 ENSESTT00000046536 Transcript downstream_gene_variant - - - - - - DISTANCE=4230 rs257383 7:106804627 T ENSESTG00000018499 ENSESTT00000046699 Transcript upstream_gene_variant - - - - - - DISTANCE=4811 rs257383 7:106804627 T CCDS5740.1 CCDS5740.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4600 rs257383 7:106804627 T 5577 NM_002736.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2371 rs257383 7:106804627 T ENSESTG00000018412 ENSESTT00000046525 Transcript downstream_gene_variant - - - - - - DISTANCE=4230 rs257383 7:106804627 T 26959 NM_001244262.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4779 rs1015685 7:107042062 C CCDS5742.1 CCDS5742.1 Transcript intron_variant - - - - - - rs1015685 7:107042062 C 10466 NM_181733.2 Transcript intron_variant - - - - - - rs1015685 7:107042062 C 10466 NM_001161520.1 Transcript intron_variant - - - - - - rs1015685 7:107042062 C ENSESTG00000018880 ENSESTT00000047933 Transcript intron_variant - - - - - - rs1015685 7:107042062 C CCDS5743.1 CCDS5743.1 Transcript intron_variant - - - - - - rs1015685 7:107042062 C ENSESTG00000018880 ENSESTT00000047892 Transcript intron_variant - - - - - - rs1015685 7:107042062 C 10466 NM_006348.3 Transcript intron_variant - - - - - - rs1015685 7:107042062 C CCDS55152.1 CCDS55152.1 Transcript intron_variant - - - - - - rs12667958 7:107092820 C CCDS5742.1 CCDS5742.1 Transcript intron_variant - - - - - - rs12667958 7:107092820 C 10466 NM_181733.2 Transcript intron_variant - - - - - - rs12667958 7:107092820 C 10466 NM_001161520.1 Transcript intron_variant - - - - - - rs12667958 7:107092820 C ENSESTG00000018880 ENSESTT00000047933 Transcript intron_variant - - - - - - rs12667958 7:107092820 C CCDS5743.1 CCDS5743.1 Transcript intron_variant - - - - - - rs12667958 7:107092820 C ENSESTG00000018880 ENSESTT00000047892 Transcript intron_variant - - - - - - rs12667958 7:107092820 C 10466 NM_006348.3 Transcript intron_variant - - - - - - rs12667958 7:107092820 C CCDS55152.1 CCDS55152.1 Transcript intron_variant - - - - - - rs6466218 7:107786189 G ENSESTG00000013780 ENSESTT00000034458 Transcript downstream_gene_variant - - - - - - DISTANCE=3839 rs6466218 7:107786189 G 4897 NM_005010.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1882 rs6466218 7:107786189 G 4897 NM_001193583.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1882 rs6466218 7:107786189 G 4897 NM_001193584.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1882 rs6466218 7:107786189 G ENSESTG00000013780 ENSESTT00000034472 Transcript downstream_gene_variant - - - - - - DISTANCE=3839 rs6466218 7:107786189 G ENSESTG00000013780 ENSESTT00000034474 Transcript downstream_gene_variant - - - - - - DISTANCE=3839 rs6466218 7:107786189 G CCDS5751.1 CCDS5751.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4166 rs6466218 7:107786189 G CCDS55153.1 CCDS55153.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4166 rs6466218 7:107786189 G 4897 NM_001037132.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1882 rs6466218 7:107786189 G CCDS47686.1 CCDS47686.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4166 rs6466218 7:107786189 G 4897 NM_001193582.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1882 rs6466218 7:107786189 G ENSESTG00000013780 ENSESTT00000034461 Transcript downstream_gene_variant - - - - - - DISTANCE=3839 rs1525024 7:108751085 T - - - intergenic_variant - - - - - - rs11982989 7:108755238 C - - - intergenic_variant - - - - - - rs4727736 7:109885602 T - - - intergenic_variant - - - - - - rs38757 7:109939589 A - - - intergenic_variant - - - - - - rs10253739 7:110217553 G - - - intergenic_variant - - - - - - rs37654 7:110994733 T CCDS5753.1 CCDS5753.1 Transcript intron_variant - - - - - - rs37654 7:110994733 T 83943 NM_001244606.1 Transcript intron_variant - - - - - - rs37654 7:110994733 T 83943 NM_032549.3 Transcript intron_variant - - - - - - rs37681 7:111043489 C CCDS5753.1 CCDS5753.1 Transcript intron_variant - - - - - - rs37681 7:111043489 C 83943 NM_001244606.1 Transcript intron_variant - - - - - - rs37681 7:111043489 C 83943 NM_032549.3 Transcript intron_variant - - - - - - rs10277630 7:111397870 T ENSESTG00000010710 ENSESTT00000026865 Transcript downstream_gene_variant - - - - - - DISTANCE=2399 rs10277630 7:111397870 T CCDS47688.1 CCDS47688.1 Transcript intron_variant - - - - - - rs10277630 7:111397870 T ENSESTG00000010710 ENSESTT00000026872 Transcript downstream_gene_variant - - - - - - DISTANCE=2461 rs10277630 7:111397870 T ENSESTG00000010710 ENSESTT00000026875 Transcript downstream_gene_variant - - - - - - DISTANCE=2461 rs10277630 7:111397870 T ENSESTG00000010710 ENSESTT00000026882 Transcript downstream_gene_variant - - - - - - DISTANCE=2410 rs10277630 7:111397870 T 9732 NM_014705.3 Transcript intron_variant - - - - - - rs10277630 7:111397870 T ENSESTG00000010710 ENSESTT00000026868 Transcript downstream_gene_variant - - - - - - DISTANCE=2399 rs10277630 7:111397870 T ENSESTG00000010710 ENSESTT00000026886 Transcript downstream_gene_variant - - - - - - DISTANCE=2461 rs10953698 7:111537804 G 9732 NM_014705.3 Transcript intron_variant - - - - - - rs10953698 7:111537804 G CCDS47688.1 CCDS47688.1 Transcript intron_variant - - - - - - rs181902 7:111620065 G ENSESTG00000010702 ENSESTT00000026795 Transcript intron_variant - - - - - - rs181902 7:111620065 G 9732 NM_014705.3 Transcript intron_variant - - - - - - rs181902 7:111620065 G CCDS47688.1 CCDS47688.1 Transcript intron_variant - - - - - - rs40385 7:111628169 T - ENSR00000632560 RegulatoryFeature regulatory_region_variant - - - - - - rs40385 7:111628169 T ENSESTG00000010702 ENSESTT00000026795 Transcript intron_variant - - - - - - rs40385 7:111628169 T 9732 NM_014705.3 Transcript intron_variant - - - - - - rs40385 7:111628169 T CCDS47688.1 CCDS47688.1 Transcript intron_variant - - - - - - rs1005660 7:112111758 C CCDS34736.1 CCDS34736.1 Transcript intron_variant - - - - - - rs1005660 7:112111758 C 3475 NM_001550.3 Transcript intron_variant - - - - - - rs1005660 7:112111758 C 3475 NM_001197079.1 Transcript intron_variant - - - - - - rs1005660 7:112111758 C ENSESTG00000010663 ENSESTT00000026719 Transcript intron_variant - - - - - - rs1005660 7:112111758 C ENSESTG00000010663 ENSESTT00000026724 Transcript intron_variant - - - - - - rs1005660 7:112111758 C CCDS56504.1 CCDS56504.1 Transcript intron_variant - - - - - - rs1005660 7:112111758 C ENSESTG00000010663 ENSESTT00000026738 Transcript intron_variant - - - - - - rs1005660 7:112111758 C 3475 NM_001197080.1 Transcript intron_variant - - - - - - rs1005660 7:112111758 C 3475 NM_001007245.2 Transcript intron_variant - - - - - - rs1005660 7:112111758 C ENSESTG00000010663 ENSESTT00000026733 Transcript intron_variant - - - - - - rs1005660 7:112111758 C ENSESTG00000010663 ENSESTT00000026704 Transcript intron_variant - - - - - - rs1718945 7:112491562 C ENSESTG00000016359 ENSESTT00000041063 Transcript intron_variant - - - - - - rs1718945 7:112491562 C CCDS43634.1 CCDS43634.1 Transcript intron_variant - - - - - - rs1718945 7:112491562 C ENSESTG00000016359 ENSESTT00000041076 Transcript intron_variant - - - - - - rs1718945 7:112491562 C 154743 NM_152556.2 Transcript intron_variant - - - - - - rs649658 7:112496115 G ENSESTG00000016359 ENSESTT00000041063 Transcript intron_variant - - - - - - rs649658 7:112496115 G CCDS43634.1 CCDS43634.1 Transcript intron_variant - - - - - - rs649658 7:112496115 G ENSESTG00000016359 ENSESTT00000041076 Transcript intron_variant - - - - - - rs649658 7:112496115 G 154743 NM_152556.2 Transcript intron_variant - - - - - - rs11983037 7:112781149 C ENSESTG00000016311 ENSESTT00000040926 Transcript upstream_gene_variant - - - - - - DISTANCE=3922 rs11983037 7:112781149 C ENSESTG00000016311 ENSESTT00000040916 Transcript intron_variant - - - - - - rs6953722 7:112890021 T - - - intergenic_variant - - - - - - rs4730582 7:113071319 C - - - intergenic_variant - - - - - - rs7790144 7:113116216 G - - - intergenic_variant - - - - - - rs2188430 7:113389048 C - - - intergenic_variant - - - - - - rs5010907 7:113455038 T - - - intergenic_variant - - - - - - rs776915 7:113793672 G ENSESTG00000006775 ENSESTT00000017267 Transcript intron_variant - - - - - - rs776915 7:113793672 G ENSESTG00000006775 ENSESTT00000017262 Transcript intron_variant - - - - - - rs776915 7:113793672 G 93986 NR_033766.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2694931 7:113971252 A ENSESTG00000006775 ENSESTT00000017267 Transcript intron_variant - - - - - - rs2694931 7:113971252 A ENSESTG00000006775 ENSESTT00000017262 Transcript intron_variant - - - - - - rs2694931 7:113971252 A 93986 NR_033766.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3934147 7:114034935 C ENSESTG00000006775 ENSESTT00000017267 Transcript intron_variant - - - - - - rs3934147 7:114034935 C ENSESTG00000006775 ENSESTT00000017262 Transcript intron_variant - - - - - - rs3934147 7:114034935 C 93986 NR_033766.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs289210 7:114446899 T - ENSR00001050371 RegulatoryFeature regulatory_region_variant - - - - - - rs289210 7:114446899 T - - - intergenic_variant - - - - - - rs2106326 7:114476115 T - - - intergenic_variant - - - - - - rs2106321 7:114535721 G - - - intergenic_variant - - - - - - rs2464889 7:114782590 A ENSESTG00000007898 ENSESTT00000019918 Transcript intron_variant - - - - - - rs2396808 7:114824648 G ENSESTG00000007898 ENSESTT00000019918 Transcript intron_variant - - - - - - rs1468151 7:114826923 C ENSESTG00000007898 ENSESTT00000019918 Transcript intron_variant - - - - - - rs7794765 7:114843438 T ENSESTG00000007898 ENSESTT00000019918 Transcript intron_variant - - - - - - rs7788779 7:114853193 C ENSESTG00000007898 ENSESTT00000019918 Transcript intron_variant - - - - - - rs1155396 7:114953865 C - - - intergenic_variant - - - - - - rs2401963 7:115258993 T - ENSR00001050379 RegulatoryFeature regulatory_region_variant - - - - - - rs2401963 7:115258993 T - - - intergenic_variant - - - - - - rs10260844 7:115536185 T - - - intergenic_variant - - - - - - rs2697058 7:115887308 G CCDS5764.1 CCDS5764.1 Transcript intron_variant - - - - - - rs2697058 7:115887308 G ENSESTG00000031018 ENSESTT00000078087 Transcript intron_variant - - - - - - rs2697058 7:115887308 G ENSESTG00000031209 ENSESTT00000078635 Transcript downstream_gene_variant - - - - - - DISTANCE=3078 rs2697058 7:115887308 G 26136 NM_152829.2 Transcript intron_variant - - - - - - rs2697058 7:115887308 G ENSESTG00000031018 ENSESTT00000078153 Transcript intron_variant - - - - - - rs2697058 7:115887308 G ENSESTG00000031018 ENSESTT00000078139 Transcript intron_variant - - - - - - rs2697058 7:115887308 G 26136 NM_015641.3 Transcript intron_variant - - - - - - rs2697058 7:115887308 G ENSESTG00000031018 ENSESTT00000078065 Transcript intron_variant - - - - - - rs2697058 7:115887308 G CCDS5763.1 CCDS5763.1 Transcript intron_variant - - - - - - rs10274093 7:116547883 C CCDS5768.1 CCDS5768.1 Transcript intron_variant - - - - - - rs10274093 7:116547883 C ENSESTG00000007897 ENSESTT00000020043 Transcript intron_variant - - - - - - rs10274093 7:116547883 C 830 NM_006136.2 Transcript intron_variant - - - - - - rs10274093 7:116547883 C ENSESTG00000007897 ENSESTT00000020063 Transcript intron_variant - - - - - - rs10274093 7:116547883 C ENSESTG00000007897 ENSESTT00000020047 Transcript intron_variant - - - - - - rs10274093 7:116547883 C ENSESTG00000007897 ENSESTT00000020059 Transcript intron_variant - - - - - - rs2402122 7:116556432 A CCDS5768.1 CCDS5768.1 Transcript intron_variant - - - - - - rs2402122 7:116556432 A ENSESTG00000007897 ENSESTT00000020043 Transcript intron_variant - - - - - - rs2402122 7:116556432 A 830 NM_006136.2 Transcript intron_variant - - - - - - rs2402122 7:116556432 A ENSESTG00000007897 ENSESTT00000020063 Transcript intron_variant - - - - - - rs2402122 7:116556432 A ENSESTG00000007897 ENSESTT00000020047 Transcript intron_variant - - - - - - rs2402122 7:116556432 A ENSESTG00000007897 ENSESTT00000020059 Transcript intron_variant - - - - - - rs6466600 7:116755209 C ENSESTG00000007971 ENSESTT00000020200 Transcript intron_variant - - - - - - rs6466600 7:116755209 C ENSESTG00000007971 ENSESTT00000020110 Transcript intron_variant - - - - - - rs6466600 7:116755209 C 7982 NM_018412.3 Transcript intron_variant - - - - - - rs6466600 7:116755209 C ENSESTG00000007971 ENSESTT00000020106 Transcript intron_variant - - - - - - rs6466600 7:116755209 C CCDS5769.1 CCDS5769.1 Transcript intron_variant - - - - - - rs6466600 7:116755209 C ENSESTG00000007971 ENSESTT00000020161 Transcript intron_variant - - - - - - rs6466600 7:116755209 C 93654 NR_002331.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs6466600 7:116755209 C ENSESTG00000007971 ENSESTT00000020206 Transcript intron_variant - - - - - - rs6466600 7:116755209 C CCDS5770.1 CCDS5770.1 Transcript intron_variant - - - - - - rs6466600 7:116755209 C 7982 NM_021908.2 Transcript intron_variant - - - - - - rs6466600 7:116755209 C ENSESTG00000007971 ENSESTT00000020155 Transcript intron_variant - - - - - - rs38897 7:116880732 A - - - intergenic_variant - - - - - - rs11983703 7:116986229 T - - - intergenic_variant - - - - - - rs4730788 7:117149761 C 1080 NM_000492.3 Transcript intron_variant - - - - - - rs4730788 7:117149761 C ENSESTG00000008026 ENSESTT00000020290 Transcript intron_variant - - - - - - rs4730788 7:117149761 C CCDS5773.1 CCDS5773.1 Transcript intron_variant - - - - - - rs213978 7:117238476 A 1080 NM_000492.3 Transcript intron_variant - - - - - - rs213978 7:117238476 A ENSESTG00000008042 ENSESTT00000020314 Transcript intron_variant - - - - - - rs213978 7:117238476 A CCDS5773.1 CCDS5773.1 Transcript intron_variant - - - - - - rs4727870 7:118083786 A - - - intergenic_variant - - - - - - rs778835 7:118303298 C - - - intergenic_variant - - - - - - rs2689727 7:118411813 A - - - intergenic_variant - - - - - - rs2699775 7:118552053 G ENSESTG00000003531 ENSESTT00000008804 Transcript intron_variant - - - - - - rs2699775 7:118552053 G ENSESTG00000003531 ENSESTT00000008824 Transcript intron_variant - - - - - - rs10275658 7:118636210 C - - - intergenic_variant - - - - - - rs2896276 7:118808575 C - - - intergenic_variant - - - - - - rs3113605 7:119005102 T - - - intergenic_variant - - - - - - rs7799185 7:119169938 T - - - intergenic_variant - - - - - - rs7795248 7:119764251 G - - - intergenic_variant - - - - - - rs6466750 7:120222741 A CCDS5776.1 CCDS5776.1 Transcript intron_variant - - - - - - rs6466750 7:120222741 A 3751 NM_012281.2 Transcript intron_variant - - - - - - rs7776794 7:120317143 G CCDS5776.1 CCDS5776.1 Transcript intron_variant - - - - - - rs7776794 7:120317143 G 3751 NM_012281.2 Transcript intron_variant - - - - - - rs1990509 7:120663194 C ENSESTG00000000015 ENSESTT00000000054 Transcript intron_variant - - - - - - rs1990509 7:120663194 C ENSESTG00000000015 ENSESTT00000000056 Transcript intron_variant - - - - - - rs1990509 7:120663194 C 79974 NM_001105533.1 Transcript intron_variant - - - - - - rs1990509 7:120663194 C 79974 NM_024913.4 Transcript intron_variant - - - - - - rs1990509 7:120663194 C ENSESTG00000000015 ENSESTT00000000051 Transcript intron_variant - - - - - - rs1990509 7:120663194 C CCDS47690.1 CCDS47690.1 Transcript intron_variant - - - - - - rs1990509 7:120663194 C CCDS34739.1 CCDS34739.1 Transcript intron_variant - - - - - - rs6651120 7:121841296 C ENSESTG00000022344 ENSESTT00000056385 Transcript intron_variant - - - - - - rs284389 7:121894111 A - - - intergenic_variant - - - - - - rs7785075 7:122114291 C ENSESTG00000022188 ENSESTT00000056183 Transcript intron_variant - - - - - - rs7785075 7:122114291 C CCDS47691.1 CCDS47691.1 Transcript intron_variant - - - - - - rs7785075 7:122114291 C CCDS55158.1 CCDS55158.1 Transcript intron_variant - - - - - - rs7785075 7:122114291 C ENSESTG00000022188 ENSESTT00000056153 Transcript intron_variant - - - - - - rs7785075 7:122114291 C 93664 NM_001009571.3 Transcript intron_variant - - - - - - rs7785075 7:122114291 C 93664 NM_017954.10 Transcript intron_variant - - - - - - rs7785075 7:122114291 C ENSESTG00000022188 ENSESTT00000056131 Transcript intron_variant - - - - - - rs7785075 7:122114291 C ENSESTG00000022188 ENSESTT00000056178 Transcript intron_variant - - - - - - rs7785075 7:122114291 C ENSESTG00000022188 ENSESTT00000056169 Transcript intron_variant - - - - - - rs7785075 7:122114291 C 93664 NM_001167940.1 Transcript intron_variant - - - - - - rs7785075 7:122114291 C ENSESTG00000022188 ENSESTT00000056113 Transcript intron_variant - - - - - - rs2251612 7:122269052 A CCDS47691.1 CCDS47691.1 Transcript intron_variant - - - - - - rs2251612 7:122269052 A CCDS55158.1 CCDS55158.1 Transcript intron_variant - - - - - - rs2251612 7:122269052 A 93664 NM_001009571.3 Transcript intron_variant - - - - - - rs2251612 7:122269052 A 93664 NM_017954.10 Transcript intron_variant - - - - - - rs2251612 7:122269052 A 93664 NM_001167940.1 Transcript intron_variant - - - - - - rs2109966 7:122358542 G CCDS47691.1 CCDS47691.1 Transcript intron_variant - - - - - - rs2109966 7:122358542 G CCDS55158.1 CCDS55158.1 Transcript intron_variant - - - - - - rs2109966 7:122358542 G ENSESTG00000022167 ENSESTT00000055870 Transcript intron_variant - - - - - - rs2109966 7:122358542 G 93664 NM_001009571.3 Transcript intron_variant - - - - - - rs2109966 7:122358542 G 93664 NM_017954.10 Transcript intron_variant - - - - - - rs2109966 7:122358542 G ENSESTG00000022167 ENSESTT00000055879 Transcript intron_variant - - - - - - rs2109966 7:122358542 G 93664 NM_001167940.1 Transcript intron_variant - - - - - - rs37891 7:122442558 C - ENSR00000633631 RegulatoryFeature regulatory_region_variant - - - - - - rs37891 7:122442558 C CCDS47691.1 CCDS47691.1 Transcript intron_variant - - - - - - rs37891 7:122442558 C CCDS55158.1 CCDS55158.1 Transcript intron_variant - - - - - - rs37891 7:122442558 C ENSESTG00000022167 ENSESTT00000055870 Transcript intron_variant - - - - - - rs37891 7:122442558 C 93664 NM_001009571.3 Transcript intron_variant - - - - - - rs37891 7:122442558 C 93664 NM_017954.10 Transcript intron_variant - - - - - - rs37891 7:122442558 C ENSESTG00000022167 ENSESTT00000055879 Transcript intron_variant - - - - - - rs37891 7:122442558 C ENSESTG00000029938 ENSESTT00000075329 Transcript intron_variant - - - - - - rs37891 7:122442558 C 93664 NM_001167940.1 Transcript intron_variant - - - - - - rs1917706 7:123091335 A 154865 NM_178827.4 Transcript downstream_gene_variant - - - - - - DISTANCE=900 rs1917706 7:123091335 A CCDS5787.1 CCDS5787.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1462 rs4624965 7:123338872 G ENSESTG00000010912 ENSESTT00000027337 Transcript intron_variant - - - - - - rs4624965 7:123338872 G 8976 NM_003941.2 Transcript intron_variant - - - - - - rs4624965 7:123338872 G ENSESTG00000010923 ENSESTT00000027392 Transcript intron_variant - - - - - - rs4624965 7:123338872 G CCDS34743.1 CCDS34743.1 Transcript intron_variant - - - - - - rs973712 7:123696292 A - - - intergenic_variant - - - - - - rs10954027 7:124117143 G - - - intergenic_variant - - - - - - rs2215157 7:124169116 G - - - intergenic_variant - - - - - - rs1404408 7:124190104 A - - - intergenic_variant - - - - - - rs2402742 7:124207419 A - - - intergenic_variant - - - - - - rs1540831 7:124244314 A - - - intergenic_variant - - - - - - rs1086918 7:125059283 T - - - intergenic_variant - - - - - - rs1358144 7:125081111 G ENSESTG00000013720 ENSESTT00000034261 Transcript intron_variant - - - - - - rs2402790 7:125348935 C - - - intergenic_variant - - - - - - rs4336552 7:125375046 A - - - intergenic_variant - - - - - - rs6976809 7:125540024 A - - - intergenic_variant - - - - - - rs4731275 7:125549911 A - - - intergenic_variant - - - - - - rs6952861 7:125556678 A - - - intergenic_variant - - - - - - rs7799318 7:125601546 C - - - intergenic_variant - - - - - - rs1011491 7:125646866 G - - - intergenic_variant - - - - - - rs511 7:126082815 G CCDS47696.1 CCDS47696.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3315 rs511 7:126082815 G 2918 NR_028041.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs511 7:126082815 G ENSESTG00000028772 ENSESTT00000072445 Transcript intron_variant - - - - - - rs511 7:126082815 G ENSESTG00000028772 ENSESTT00000072464 Transcript intron_variant - - - - - - rs511 7:126082815 G ENSESTG00000028772 ENSESTT00000072425 Transcript intron_variant - - - - - - rs511 7:126082815 G 2918 NM_000845.2 Transcript intron_variant - - - - - - rs511 7:126082815 G 2918 NM_001127323.1 Transcript intron_variant - - - - - - rs511 7:126082815 G CCDS5794.1 CCDS5794.1 Transcript intron_variant - - - - - - rs512 7:126089670 C - ENSR00001563608 RegulatoryFeature regulatory_region_variant - - - - - - rs512 7:126089670 C CCDS47696.1 CCDS47696.1 Transcript intron_variant - - - - - - rs512 7:126089670 C 2918 NR_028041.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs512 7:126089670 C ENSESTG00000028772 ENSESTT00000072445 Transcript upstream_gene_variant - - - - - - DISTANCE=3238 rs512 7:126089670 C ENSESTG00000028772 ENSESTT00000072464 Transcript upstream_gene_variant - - - - - - DISTANCE=3242 rs512 7:126089670 C ENSESTG00000028772 ENSESTT00000072425 Transcript upstream_gene_variant - - - - - - DISTANCE=2425 rs512 7:126089670 C 2918 NM_000845.2 Transcript intron_variant - - - - - - rs512 7:126089670 C 2918 NM_001127323.1 Transcript intron_variant - - - - - - rs512 7:126089670 C CCDS5794.1 CCDS5794.1 Transcript intron_variant - - - - - - rs515 7:126116798 C CCDS47696.1 CCDS47696.1 Transcript intron_variant - - - - - - rs515 7:126116798 C 2918 NM_000845.2 Transcript intron_variant - - - - - - rs515 7:126116798 C 2918 NR_028041.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs515 7:126116798 C CCDS5794.1 CCDS5794.1 Transcript intron_variant - - - - - - rs515 7:126116798 C 2918 NM_001127323.1 Transcript intron_variant - - - - - - rs518 7:126129104 A CCDS47696.1 CCDS47696.1 Transcript intron_variant - - - - - - rs518 7:126129104 A 2918 NM_000845.2 Transcript intron_variant - - - - - - rs518 7:126129104 A 2918 NR_028041.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs518 7:126129104 A CCDS5794.1 CCDS5794.1 Transcript intron_variant - - - - - - rs518 7:126129104 A 2918 NM_001127323.1 Transcript intron_variant - - - - - - rs1557666 7:126259722 T CCDS47696.1 CCDS47696.1 Transcript intron_variant - - - - - - rs1557666 7:126259722 T 2918 NM_000845.2 Transcript intron_variant - - - - - - rs1557666 7:126259722 T 2918 NR_028041.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1557666 7:126259722 T CCDS5794.1 CCDS5794.1 Transcript intron_variant - - - - - - rs1557666 7:126259722 T 2918 NM_001127323.1 Transcript intron_variant - - - - - - rs9655860 7:126314795 G CCDS47696.1 CCDS47696.1 Transcript intron_variant - - - - - - rs9655860 7:126314795 G 2918 NM_000845.2 Transcript intron_variant - - - - - - rs9655860 7:126314795 G 2918 NR_028041.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9655860 7:126314795 G CCDS5794.1 CCDS5794.1 Transcript intron_variant - - - - - - rs9655860 7:126314795 G 2918 NM_001127323.1 Transcript intron_variant - - - - - - rs978873 7:126663988 G CCDS47696.1 CCDS47696.1 Transcript intron_variant - - - - - - rs978873 7:126663988 G 2918 NM_000845.2 Transcript intron_variant - - - - - - rs978873 7:126663988 G 2918 NR_028041.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs978873 7:126663988 G CCDS5794.1 CCDS5794.1 Transcript intron_variant - - - - - - rs978873 7:126663988 G 2918 NM_001127323.1 Transcript intron_variant - - - - - - rs1592364 7:126888421 G 2918 NM_000845.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4852 rs1592364 7:126888421 G 2918 NR_028041.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4852 rs1592364 7:126888421 G ENSESTG00000001452 ENSESTT00000003437 Transcript intron_variant - - - - - - rs1592364 7:126888421 G 2918 NM_001127323.1 Transcript intron_variant - - - - - - rs9649508 7:126940941 G - - - intergenic_variant - - - - - - rs4731408 7:127804813 A - ENSR00000633990 RegulatoryFeature regulatory_region_variant - - - - - - rs4731408 7:127804813 A - - - intergenic_variant - - - - - - rs806543 7:127867632 C ENSESTG00000033714 ENSESTT00000085249 Transcript downstream_gene_variant - - - - - - DISTANCE=3160 rs13308199 7:128315588 C ENSESTG00000022835 ENSESTT00000057614 Transcript upstream_gene_variant - - - - - - DISTANCE=4589 rs13308199 7:128315588 C 346653 NM_001012454.3 Transcript intron_variant - - - - - - rs13308199 7:128315588 C CCDS47701.1 CCDS47701.1 Transcript intron_variant - - - - - - rs13308199 7:128315588 C CCDS47702.1 CCDS47702.1 Transcript intron_variant - - - - - - rs13308199 7:128315588 C 346653 NM_001128926.1 Transcript intron_variant - - - - - - rs13308199 7:128315588 C ENSESTG00000022835 ENSESTT00000057597 Transcript intron_variant - - - - - - rs13308199 7:128315588 C ENSESTG00000022835 ENSESTT00000057573 Transcript intron_variant - - - - - - rs4731614 7:129325929 G CCDS5813.2 CCDS5813.2 Transcript intron_variant - - - - - - rs4731614 7:129325929 G 4899 NM_005011.3 Transcript intron_variant - - - - - - rs4731614 7:129325929 G ENSESTG00000007420 ENSESTT00000018690 Transcript intron_variant - - - - - - rs4731614 7:129325929 G ENSESTG00000024475 ENSESTT00000061986 Transcript intron_variant - - - - - - rs4731614 7:129325929 G 4899 NM_001040110.1 Transcript intron_variant - - - - - - rs4731614 7:129325929 G ENSESTG00000024475 ENSESTT00000062024 Transcript intron_variant - - - - - - rs6962258 7:129362407 C ENSESTG00000007420 ENSESTT00000018692 Transcript intron_variant - - - - - - rs6962258 7:129362407 C CCDS5813.2 CCDS5813.2 Transcript intron_variant - - - - - - rs6962258 7:129362407 C 4899 NM_005011.3 Transcript intron_variant - - - - - - rs6962258 7:129362407 C ENSESTG00000007420 ENSESTT00000018690 Transcript intron_variant - - - - - - rs6962258 7:129362407 C 4899 NM_001040110.1 Transcript intron_variant - - - - - - rs6962258 7:129362407 C ENSESTG00000007420 ENSESTT00000018697 Transcript intron_variant - - - - - - rs6962258 7:129362407 C ENSESTG00000024475 ENSESTT00000062024 Transcript intron_variant - - - - - - rs6965346 7:130067576 T CCDS59078.1 CCDS59078.1 Transcript intron_variant - - - - - - rs6965346 7:130067576 T ENSESTG00000007698 ENSESTT00000019415 Transcript intron_variant - - - - - - rs6965346 7:130067576 T ENSESTG00000007698 ENSESTT00000019407 Transcript intron_variant - - - - - - rs6965346 7:130067576 T CCDS59080.1 CCDS59080.1 Transcript intron_variant - - - - - - rs6965346 7:130067576 T ENSESTG00000007698 ENSESTT00000019424 Transcript intron_variant - - - - - - rs6965346 7:130067576 T 95681 NM_001257158.1 Transcript intron_variant - - - - - - rs6965346 7:130067576 T ENSESTG00000007698 ENSESTT00000019426 Transcript intron_variant - - - - - - rs6965346 7:130067576 T ENSESTG00000007698 ENSESTT00000019404 Transcript intron_variant - - - - - - rs6965346 7:130067576 T ENSESTG00000007698 ENSESTT00000019435 Transcript upstream_gene_variant - - - - - - DISTANCE=990 rs6965346 7:130067576 T 95681 NM_001257160.1 Transcript intron_variant - - - - - - rs6965346 7:130067576 T 95681 NM_018718.2 Transcript intron_variant - - - - - - rs6965346 7:130067576 T 95681 NR_046443.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6965346 7:130067576 T 95681 NM_001257159.1 Transcript intron_variant - - - - - - rs6965346 7:130067576 T CCDS5821.1 CCDS5821.1 Transcript intron_variant - - - - - - rs6965346 7:130067576 T CCDS59079.1 CCDS59079.1 Transcript intron_variant - - - - - - rs6968284 7:130138155 G ENSESTG00000007656 ENSESTT00000019372 Transcript upstream_gene_variant - - - - - - DISTANCE=85 rs6968284 7:130138155 G 4232 NM_001253901.1 Transcript intron_variant - - - - - - rs6968284 7:130138155 G ENSESTG00000007656 ENSESTT00000019349 Transcript intron_variant - - - - - - rs6968284 7:130138155 G ENSESTG00000007656 ENSESTT00000019361 Transcript intron_variant - - - - - - rs6968284 7:130138155 G 442904 NR_029899.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2110 rs6968284 7:130138155 G ENSESTG00000007656 ENSESTT00000019354 Transcript intron_variant - - - - - - rs6968284 7:130138155 G 4232 NM_001253902.1 Transcript intron_variant - - - - - - rs6968284 7:130138155 G ENSESTG00000007656 ENSESTT00000019332 Transcript intron_variant - - - - - - rs6968284 7:130138155 G ENSESTG00000007656 ENSESTT00000019345 Transcript intron_variant - - - - - - rs6968284 7:130138155 G 4232 NM_177524.2 Transcript intron_variant - - - - - - rs6968284 7:130138155 G ENSESTG00000007656 ENSESTT00000019368 Transcript intron_variant - - - - - - rs6968284 7:130138155 G 4232 NM_002402.3 Transcript intron_variant - - - - - - rs6968284 7:130138155 G 4232 NM_177525.2 Transcript intron_variant - - - - - - rs6968284 7:130138155 G CCDS5823.1 CCDS5823.1 Transcript intron_variant - - - - - - rs6968284 7:130138155 G CCDS59081.1 CCDS59081.1 Transcript intron_variant - - - - - - rs6968284 7:130138155 G 4232 NM_001253900.1 Transcript intron_variant - - - - - - rs6968284 7:130138155 G CCDS5822.1 CCDS5822.1 Transcript intron_variant - - - - - - rs6968284 7:130138155 G ENSESTG00000007656 ENSESTT00000019365 Transcript intron_variant - - - - - - rs1685761 7:130332513 T 26958 NM_012133.4 Transcript intron_variant - - - - - - rs1685761 7:130332513 T ENSESTG00000027265 ENSESTT00000068874 Transcript intron_variant - - - - - - rs1685761 7:130332513 T ENSESTG00000027265 ENSESTT00000068831 Transcript intron_variant - - - - - - rs350636 7:130703545 G ENSESTG00000027139 ENSESTT00000068432 Transcript intron_variant - - - - - - rs350636 7:130703545 G ENSESTG00000027139 ENSESTT00000068543 Transcript intron_variant - - - - - - rs350636 7:130703545 G ENSESTG00000027139 ENSESTT00000068523 Transcript intron_variant - - - - - - rs350636 7:130703545 G ENSESTG00000027139 ENSESTT00000068422 Transcript intron_variant - - - - - - rs350636 7:130703545 G 378805 NR_015431.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs350636 7:130703545 G ENSESTG00000027139 ENSESTT00000068500 Transcript intron_variant - - - - - - rs350636 7:130703545 G 378805 NR_024153.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs350636 7:130703545 G ENSESTG00000027139 ENSESTT00000068448 Transcript intron_variant - - - - - - rs350636 7:130703545 G ENSESTG00000027139 ENSESTT00000068463 Transcript intron_variant - - - - - - rs2598187 7:130971063 A 4289 NM_001145354.1 Transcript intron_variant - - - - - - rs2598187 7:130971063 A ENSESTG00000026822 ENSESTT00000067748 Transcript intron_variant - - - - - - rs2598187 7:130971063 A ENSESTG00000026822 ENSESTT00000067760 Transcript intron_variant - - - - - - rs1487254 7:131023463 A CCDS34754.1 CCDS34754.1 Transcript intron_variant - - - - - - rs1487254 7:131023463 A ENSESTG00000026822 ENSESTT00000067800 Transcript intron_variant - - - - - - rs1487254 7:131023463 A 4289 NM_001145354.1 Transcript intron_variant - - - - - - rs1487254 7:131023463 A ENSESTG00000026822 ENSESTT00000067748 Transcript intron_variant - - - - - - rs1487254 7:131023463 A ENSESTG00000026822 ENSESTT00000067851 Transcript intron_variant - - - - - - rs1487254 7:131023463 A 4289 NM_013255.4 Transcript intron_variant - - - - - - rs1487254 7:131023463 A ENSESTG00000026822 ENSESTT00000067832 Transcript intron_variant - - - - - - rs1487254 7:131023463 A ENSESTG00000026822 ENSESTT00000067760 Transcript intron_variant - - - - - - rs1643261 7:131210471 T - ENSR00000634474 RegulatoryFeature regulatory_region_variant - - - - - - rs1643261 7:131210471 T CCDS34755.1 CCDS34755.1 Transcript intron_variant - - - - - - rs1643261 7:131210471 T ENSESTG00000027111 ENSESTT00000068314 Transcript intron_variant - - - - - - rs1643261 7:131210471 T CCDS47714.1 CCDS47714.1 Transcript intron_variant - - - - - - rs1643261 7:131210471 T 5420 NM_005397.3 Transcript intron_variant - - - - - - rs1643261 7:131210471 T ENSESTG00000027111 ENSESTT00000068349 Transcript intron_variant - - - - - - rs1643261 7:131210471 T 5420 NM_001018111.2 Transcript intron_variant - - - - - - rs2671094 7:131826973 G ENSESTG00000033644 ENSESTT00000085049 Transcript intron_variant - - - - - - rs2671094 7:131826973 G CCDS43646.1 CCDS43646.1 Transcript intron_variant - - - - - - rs2671094 7:131826973 G 91584 NM_020911.1 Transcript intron_variant - - - - - - rs12113530 7:132491242 A CCDS5828.1 CCDS5828.1 Transcript intron_variant - - - - - - rs12113530 7:132491242 A 54927 NM_017812.2 Transcript intron_variant - - - - - - rs6951418 7:132767617 A ENSESTG00000021829 ENSESTT00000054933 Transcript upstream_gene_variant - - - - - - DISTANCE=740 rs6951418 7:132767617 A CCDS5828.1 CCDS5828.1 Transcript upstream_gene_variant - - - - - - DISTANCE=920 rs6951418 7:132767617 A 54927 NM_017812.2 Transcript upstream_gene_variant - - - - - - DISTANCE=784 rs6951418 7:132767617 A ENSESTG00000021684 ENSESTT00000054444 Transcript downstream_gene_variant - - - - - - DISTANCE=405 rs10281540 7:132853290 G - - - intergenic_variant - - - - - - rs10273178 7:132858477 G - - - intergenic_variant - - - - - - rs4308659 7:132908372 C - - - intergenic_variant - - - - - - rs4620208 7:132909495 T - - - intergenic_variant - - - - - - rs12533899 7:133150436 C CCDS43648.1 CCDS43648.1 Transcript intron_variant - - - - - - rs12533899 7:133150436 C ENSESTG00000021695 ENSESTT00000054762 Transcript intron_variant - - - - - - rs12533899 7:133150436 C 60412 NM_021807.3 Transcript intron_variant - - - - - - rs12533899 7:133150436 C ENSESTG00000021695 ENSESTT00000054655 Transcript intron_variant - - - - - - rs12533899 7:133150436 C ENSESTG00000021695 ENSESTT00000054684 Transcript intron_variant - - - - - - rs12533899 7:133150436 C ENSESTG00000021695 ENSESTT00000054724 Transcript intron_variant - - - - - - rs12533899 7:133150436 C ENSESTG00000021695 ENSESTT00000054732 Transcript intron_variant - - - - - - rs12533899 7:133150436 C CCDS5829.1 CCDS5829.1 Transcript intron_variant - - - - - - rs12533899 7:133150436 C 60412 NM_001037126.1 Transcript intron_variant - - - - - - rs722231 7:133228780 A ENSESTG00000021695 ENSESTT00000054762 Transcript intron_variant - - - - - - rs722231 7:133228780 A ENSESTG00000021695 ENSESTT00000054790 Transcript intron_variant - - - - - - rs722231 7:133228780 A ENSESTG00000021695 ENSESTT00000054772 Transcript intron_variant - - - - - - rs722231 7:133228780 A ENSESTG00000021695 ENSESTT00000054724 Transcript intron_variant - - - - - - rs722231 7:133228780 A ENSESTG00000021695 ENSESTT00000054655 Transcript intron_variant - - - - - - rs722231 7:133228780 A 60412 NM_021807.3 Transcript intron_variant - - - - - - rs722231 7:133228780 A CCDS5829.1 CCDS5829.1 Transcript intron_variant - - - - - - rs9656433 7:133735399 A ENSESTG00000026508 ENSESTT00000066860 Transcript intron_variant - - - - - - rs9656433 7:133735399 A ENSESTG00000026508 ENSESTT00000066948 Transcript intron_variant - - - - - - rs9656433 7:133735399 A ENSESTG00000026508 ENSESTT00000066975 Transcript intron_variant - - - - - - rs9656433 7:133735399 A ENSESTG00000026508 ENSESTT00000066920 Transcript intron_variant - - - - - - rs9656433 7:133735399 A 60412 NM_021807.3 Transcript intron_variant - - - - - - rs9656433 7:133735399 A ENSESTG00000027018 ENSESTT00000068079 Transcript intron_variant - - - - - - rs9656433 7:133735399 A CCDS5829.1 CCDS5829.1 Transcript intron_variant - - - - - - rs11769652 7:133787453 A - - - intergenic_variant - - - - - - rs1222416 7:133886725 C - ENSR00001564096 RegulatoryFeature regulatory_region_variant - - - - - - rs1222416 7:133886725 C 136332 NM_144648.1 Transcript intron_variant - - - - - - rs1222416 7:133886725 C CCDS5830.1 CCDS5830.1 Transcript intron_variant - - - - - - rs1222415 7:133887185 C 136332 NM_144648.1 Transcript intron_variant - - - - - - rs1222415 7:133887185 C CCDS5830.1 CCDS5830.1 Transcript intron_variant - - - - - - rs2598287 7:133976232 C ENSESTG00000026937 ENSESTT00000068025 Transcript downstream_gene_variant - - - - - - DISTANCE=141 rs2598287 7:133976232 C CCDS34756.1 CCDS34756.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3353 rs2598287 7:133976232 C 84912 NM_032826.4 Transcript 3_prime_UTR_variant 4673 - - - - - rs2598287 7:133976232 C ENSESTG00000026937 ENSESTT00000068065 Transcript downstream_gene_variant - - - - - - DISTANCE=3421 rs2598287 7:133976232 C ENSESTG00000026937 ENSESTT00000068060 Transcript downstream_gene_variant - - - - - - DISTANCE=571 rs1732037 7:134131504 G ENSESTG00000026752 ENSESTT00000067814 Transcript intron_variant - - - - - - rs1732037 7:134131504 G ENSESTG00000026752 ENSESTT00000067863 Transcript intron_variant - - - - - - rs1732037 7:134131504 G CCDS5831.1 CCDS5831.1 Transcript intron_variant - - - - - - rs1732037 7:134131504 G 231 NM_001628.2 Transcript intron_variant - - - - - - rs1732037 7:134131504 G ENSESTG00000026752 ENSESTT00000067844 Transcript downstream_gene_variant - - - - - - DISTANCE=2909 rs1732035 7:134136584 C ENSESTG00000026752 ENSESTT00000067814 Transcript intron_variant - - - - - - rs1732035 7:134136584 C ENSESTG00000026752 ENSESTT00000067863 Transcript intron_variant - - - - - - rs1732035 7:134136584 C CCDS5831.1 CCDS5831.1 Transcript intron_variant - - - - - - rs1732035 7:134136584 C 231 NM_001628.2 Transcript intron_variant - - - - - - rs1732035 7:134136584 C ENSESTG00000026752 ENSESTT00000067844 Transcript intron_variant - - - - - - rs1708402 7:134161222 A - - - intergenic_variant - - - - - - rs1790997 7:134179144 T - - - intergenic_variant - - - - - - rs1025096 7:134344182 G ENSESTG00000001465 ENSESTT00000003490 Transcript upstream_gene_variant - - - - - - DISTANCE=991 rs1025096 7:134344182 G ENSESTG00000001465 ENSESTT00000003469 Transcript intron_variant - - - - - - rs1025096 7:134344182 G 669 NM_001724.4 Transcript intron_variant - - - - - - rs1025096 7:134344182 G CCDS5833.1 CCDS5833.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2078 rs1025096 7:134344182 G ENSESTG00000001465 ENSESTT00000003483 Transcript intron_variant - - - - - - rs1025096 7:134344182 G 669 NM_199186.2 Transcript intron_variant - - - - - - rs1025096 7:134344182 G ENSESTG00000001465 ENSESTT00000003479 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003698 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003765 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003757 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003752 Transcript intron_variant - - - - - - rs10241327 7:134544305 C 800 NM_004342.6 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003701 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003702 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003764 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003721 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003736 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003762 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003683 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003706 Transcript intron_variant - - - - - - rs10241327 7:134544305 C 800 NM_033157.3 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003760 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003749 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003742 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003743 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003734 Transcript intron_variant - - - - - - rs10241327 7:134544305 C 800 NM_033138.3 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003739 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003766 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003691 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003759 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003737 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003755 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003719 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003741 Transcript intron_variant - - - - - - rs10241327 7:134544305 C ENSESTG00000001513 ENSESTT00000003744 Transcript intron_variant - - - - - - rs7801528 7:134736153 G CCDS47718.1 CCDS47718.1 Transcript intron_variant - - - - - - rs7801528 7:134736153 G 340351 NM_178563.3 Transcript intron_variant - - - - - - rs2348271 7:134786796 C CCDS47718.1 CCDS47718.1 Transcript intron_variant - - - - - - rs2348271 7:134786796 C 340351 NM_178563.3 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004045 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004032 Transcript intron_variant - - - - - - rs1030292 7:135067302 A CCDS43650.1 CCDS43650.1 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004046 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004005 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004030 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004056 Transcript intron_variant - - - - - - rs1030292 7:135067302 A CCDS55164.1 CCDS55164.1 Transcript intron_variant - - - - - - rs1030292 7:135067302 A 4850 NM_013316.3 Transcript intron_variant - - - - - - rs1030292 7:135067302 A 4850 NM_001190847.1 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004044 Transcript intron_variant - - - - - - rs1030292 7:135067302 A CCDS55167.1 CCDS55167.1 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004060 Transcript intron_variant - - - - - - rs1030292 7:135067302 A 4850 NM_001190849.1 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004035 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004061 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004072 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000003999 Transcript intron_variant - - - - - - rs1030292 7:135067302 A CCDS55165.1 CCDS55165.1 Transcript intron_variant - - - - - - rs1030292 7:135067302 A 4850 NM_001190850.1 Transcript intron_variant - - - - - - rs1030292 7:135067302 A ENSESTG00000001647 ENSESTT00000004002 Transcript intron_variant - - - - - - rs1030292 7:135067302 A 4850 NM_001190848.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4520 rs1030292 7:135067302 A 4850 NM_001008225.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4520 rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004045 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004026 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004050 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004037 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004032 Transcript intron_variant - - - - - - rs2551758 7:135090968 A CCDS43650.1 CCDS43650.1 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004046 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004047 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004030 Transcript intron_variant - - - - - - rs2551758 7:135090968 A CCDS55164.1 CCDS55164.1 Transcript intron_variant - - - - - - rs2551758 7:135090968 A 4850 NM_013316.3 Transcript intron_variant - - - - - - rs2551758 7:135090968 A 4850 NM_001190847.1 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004044 Transcript intron_variant - - - - - - rs2551758 7:135090968 A 4850 NM_001190849.1 Transcript intron_variant - - - - - - rs2551758 7:135090968 A CCDS47719.1 CCDS47719.1 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004035 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004061 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004048 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004024 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000003999 Transcript intron_variant - - - - - - rs2551758 7:135090968 A 4850 NM_001190850.1 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004036 Transcript intron_variant - - - - - - rs2551758 7:135090968 A 4850 NM_001190848.1 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004065 Transcript intron_variant - - - - - - rs2551758 7:135090968 A CCDS55166.1 CCDS55166.1 Transcript intron_variant - - - - - - rs2551758 7:135090968 A 4850 NM_001008225.2 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004022 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004064 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004005 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004056 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004038 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004068 Transcript intron_variant - - - - - - rs2551758 7:135090968 A CCDS55167.1 CCDS55167.1 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004060 Transcript intron_variant - - - - - - rs2551758 7:135090968 A ENSESTG00000001647 ENSESTT00000004002 Transcript intron_variant - - - - - - rs2551758 7:135090968 A CCDS55165.1 CCDS55165.1 Transcript intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004045 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004026 Transcript synonymous_variant 1111 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004050 Transcript synonymous_variant 1158 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004037 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004032 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G CCDS43650.1 CCDS43650.1 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004046 Transcript synonymous_variant 1158 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004047 Transcript synonymous_variant 1158 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004030 Transcript synonymous_variant 1023 816 272 Y taT/taC - rs2696877 7:135095270 G CCDS55164.1 CCDS55164.1 Transcript synonymous_variant 816 816 272 Y taT/taC - rs2696877 7:135095270 G 4850 NM_013316.3 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G 4850 NM_001190847.1 Transcript synonymous_variant 1147 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004044 Transcript synonymous_variant 1158 816 272 Y taT/taC - rs2696877 7:135095270 G 4850 NM_001190849.1 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G CCDS47719.1 CCDS47719.1 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004035 Transcript synonymous_variant 1023 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004061 Transcript synonymous_variant 1047 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004048 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004024 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000003999 Transcript synonymous_variant 1111 816 272 Y taT/taC - rs2696877 7:135095270 G 4850 NM_001190850.1 Transcript synonymous_variant 1147 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004036 Transcript synonymous_variant 1023 816 272 Y taT/taC - rs2696877 7:135095270 G 4850 NM_001190848.1 Transcript synonymous_variant 1147 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004065 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G CCDS55166.1 CCDS55166.1 Transcript synonymous_variant 816 816 272 Y taT/taC - rs2696877 7:135095270 G 4850 NM_001008225.2 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004022 Transcript synonymous_variant 1111 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004064 Transcript synonymous_variant 1047 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004005 Transcript synonymous_variant 1111 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004056 Transcript synonymous_variant 1047 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004038 Transcript synonymous_variant 1023 816 272 Y taT/taC - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004068 Transcript synonymous_variant 1047 816 272 Y taT/taC - rs2696877 7:135095270 G CCDS55167.1 CCDS55167.1 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004060 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G ENSESTG00000001647 ENSESTT00000004002 Transcript splice_region_variant,intron_variant - - - - - - rs2696877 7:135095270 G CCDS55165.1 CCDS55165.1 Transcript synonymous_variant 816 816 272 Y taT/taC - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004045 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004026 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004050 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004037 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004032 Transcript intron_variant - - - - - - rs2718166 7:135124896 T CCDS43650.1 CCDS43650.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1817 rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004046 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004047 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004030 Transcript intron_variant - - - - - - rs2718166 7:135124896 T CCDS55164.1 CCDS55164.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1817 rs2718166 7:135124896 T 4850 NM_013316.3 Transcript intron_variant - - - - - - rs2718166 7:135124896 T 4850 NM_001190847.1 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004044 Transcript intron_variant - - - - - - rs2718166 7:135124896 T 4850 NM_001190849.1 Transcript intron_variant - - - - - - rs2718166 7:135124896 T CCDS47719.1 CCDS47719.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1817 rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004035 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004061 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004048 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004024 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000003999 Transcript intron_variant - - - - - - rs2718166 7:135124896 T 4850 NM_001190850.1 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004036 Transcript intron_variant - - - - - - rs2718166 7:135124896 T 4850 NM_001190848.1 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004065 Transcript intron_variant - - - - - - rs2718166 7:135124896 T CCDS55166.1 CCDS55166.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1817 rs2718166 7:135124896 T 4850 NM_001008225.2 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004022 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004064 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004005 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004056 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004038 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004068 Transcript intron_variant - - - - - - rs2718166 7:135124896 T CCDS55167.1 CCDS55167.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1817 rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004060 Transcript intron_variant - - - - - - rs2718166 7:135124896 T ENSESTG00000001647 ENSESTT00000004002 Transcript intron_variant - - - - - - rs2718166 7:135124896 T CCDS55165.1 CCDS55165.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1817 rs4410839 7:135276485 A ENSESTG00000029863 ENSESTT00000075933 Transcript upstream_gene_variant - - - - - - DISTANCE=2799 rs4410839 7:135276485 A ENSESTG00000029863 ENSESTT00000075758 Transcript intron_variant - - - - - - rs4410839 7:135276485 A CCDS34759.1 CCDS34759.1 Transcript intron_variant - - - - - - rs4410839 7:135276485 A 23165 NM_015135.2 Transcript intron_variant - - - - - - rs4732133 7:135301015 G - ENSR00000634925 RegulatoryFeature regulatory_region_variant - - - - - - rs4732133 7:135301015 G ENSESTG00000029863 ENSESTT00000075933 Transcript intron_variant - - - - - - rs4732133 7:135301015 G ENSESTG00000029863 ENSESTT00000075758 Transcript intron_variant - - - - - - rs4732133 7:135301015 G CCDS34759.1 CCDS34759.1 Transcript intron_variant - - - - - - rs4732133 7:135301015 G ENSESTG00000029863 ENSESTT00000075943 Transcript intron_variant - - - - - - rs4732133 7:135301015 G 23165 NM_015135.2 Transcript intron_variant - - - - - - rs4415261 7:135333572 T ENSESTG00000029863 ENSESTT00000075960 Transcript downstream_gene_variant - - - - - - DISTANCE=3231 rs4415261 7:135333572 T ENSESTG00000029863 ENSESTT00000075950 Transcript downstream_gene_variant - - - - - - DISTANCE=3231 rs4415261 7:135333572 T ENSESTG00000029863 ENSESTT00000075758 Transcript downstream_gene_variant - - - - - - DISTANCE=3231 rs4415261 7:135333572 T CCDS34759.1 CCDS34759.1 Transcript downstream_gene_variant - - - - - - DISTANCE=268 rs4415261 7:135333572 T ENSESTG00000030194 ENSESTT00000076002 Transcript downstream_gene_variant - - - - - - DISTANCE=80 rs4415261 7:135333572 T ENSESTG00000029863 ENSESTT00000075933 Transcript downstream_gene_variant - - - - - - DISTANCE=3231 rs4415261 7:135333572 T ENSESTG00000029863 ENSESTT00000075943 Transcript downstream_gene_variant - - - - - - DISTANCE=3231 rs4415261 7:135333572 T 23165 NM_015135.2 Transcript downstream_gene_variant - - - - - - DISTANCE=71 rs834796 7:135866091 A - - - intergenic_variant - - - - - - rs6467655 7:136094254 A - - - intergenic_variant - - - - - - rs6467664 7:136163261 A - - - intergenic_variant - - - - - - rs10269743 7:136291618 A - - - intergenic_variant - - - - - - rs10480519 7:136293790 A - - - intergenic_variant - - - - - - rs6467685 7:136431341 A - - - intergenic_variant - - - - - - rs1424573 7:136549638 C ENSESTG00000015322 ENSESTT00000038384 Transcript upstream_gene_variant - - - - - - DISTANCE=3766 rs1424573 7:136549638 C 1129 NM_001006627.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3761 rs1424573 7:136549638 C 1129 NM_001006629.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4346 rs1424573 7:136549638 C ENSESTG00000015322 ENSESTT00000038393 Transcript upstream_gene_variant - - - - - - DISTANCE=4194 rs1424573 7:136549638 C 1129 NM_001006630.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3761 rs1424573 7:136549638 C 1129 NM_001006631.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4194 rs1424573 7:136549638 C ENSESTG00000015322 ENSESTT00000038390 Transcript upstream_gene_variant - - - - - - DISTANCE=4194 rs1424573 7:136549638 C 1129 NM_001006628.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4355 rs1424573 7:136549638 C 1129 NM_001006632.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4194 rs1424573 7:136549638 C 1129 NM_001006626.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4231 rs1424573 7:136549638 C 1129 NM_000739.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4194 rs324652 7:136703707 T 349160 NR_046103.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs324652 7:136703707 T ENSESTG00000015322 ENSESTT00000038384 Transcript downstream_gene_variant - - - - - - DISTANCE=3441 rs324652 7:136703707 T 1129 NM_001006627.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs324652 7:136703707 T 1129 NM_001006629.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs324652 7:136703707 T 1129 NM_001006630.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs324652 7:136703707 T CCDS5843.1 CCDS5843.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2694 rs324652 7:136703707 T 1129 NM_001006631.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs324652 7:136703707 T 1129 NM_001006628.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs324652 7:136703707 T 1129 NM_001006632.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs324652 7:136703707 T 1129 NM_001006626.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs324652 7:136703707 T 1129 NM_000739.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1936 rs10234040 7:136784740 A 349160 NR_046103.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1162122 7:136939582 T ENSESTG00000015338 ENSESTT00000038470 Transcript intron_variant - - - - - - rs1162122 7:136939582 T CCDS5844.1 CCDS5844.1 Transcript intron_variant - - - - - - rs1162122 7:136939582 T 5764 NM_002825.5 Transcript intron_variant - - - - - - rs1669045 7:136962251 A ENSESTG00000015338 ENSESTT00000038470 Transcript intron_variant - - - - - - rs1669045 7:136962251 A 5764 NM_002825.5 Transcript intron_variant - - - - - - rs1731953 7:136986500 T ENSESTG00000015338 ENSESTT00000038470 Transcript intron_variant - - - - - - rs1731953 7:136986500 T 5764 NM_002825.5 Transcript intron_variant - - - - - - rs2432720 7:137042470 T - - - intergenic_variant - - - - - - rs1669023 7:137061577 T - - - intergenic_variant - - - - - - rs1620590 7:137074644 C CCDS5845.1 CCDS5845.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1322 rs1620590 7:137074644 C 9162 NM_004717.2 Transcript 3_prime_UTR_variant 4521 - - - - - rs1647182 7:137090153 T CCDS5845.1 CCDS5845.1 Transcript intron_variant - - - - - - rs1647182 7:137090153 T 9162 NM_004717.2 Transcript intron_variant - - - - - - rs1918836 7:137190082 C CCDS5845.1 CCDS5845.1 Transcript intron_variant - - - - - - rs1918836 7:137190082 C 9162 NM_004717.2 Transcript intron_variant - - - - - - rs1723112 7:137302031 T CCDS5845.1 CCDS5845.1 Transcript intron_variant - - - - - - rs1723112 7:137302031 T 9162 NM_004717.2 Transcript intron_variant - - - - - - rs1723112 7:137302031 T ENSESTG00000029065 ENSESTT00000073289 Transcript downstream_gene_variant - - - - - - DISTANCE=2569 rs1723112 7:137302031 T ENSESTG00000029065 ENSESTT00000073200 Transcript intron_variant - - - - - - rs1646354 7:137302105 G CCDS5845.1 CCDS5845.1 Transcript intron_variant - - - - - - rs1646354 7:137302105 G 9162 NM_004717.2 Transcript intron_variant - - - - - - rs1646354 7:137302105 G ENSESTG00000029065 ENSESTT00000073289 Transcript downstream_gene_variant - - - - - - DISTANCE=2495 rs1646354 7:137302105 G ENSESTG00000029065 ENSESTT00000073200 Transcript intron_variant - - - - - - rs270890 7:137381239 A - ENSR00001564345 RegulatoryFeature regulatory_region_variant - - - - - - rs270890 7:137381239 A ENSESTG00000029065 ENSESTT00000073233 Transcript intron_variant - - - - - - rs270890 7:137381239 A CCDS5845.1 CCDS5845.1 Transcript intron_variant - - - - - - rs270890 7:137381239 A 9162 NM_004717.2 Transcript intron_variant - - - - - - rs270890 7:137381239 A ENSESTG00000029065 ENSESTT00000073255 Transcript intron_variant - - - - - - rs270890 7:137381239 A ENSESTG00000029065 ENSESTT00000073200 Transcript intron_variant - - - - - - rs4732266 7:137442765 A ENSESTG00000029065 ENSESTT00000073233 Transcript intron_variant - - - - - - rs4732266 7:137442765 A CCDS5845.1 CCDS5845.1 Transcript intron_variant - - - - - - rs4732266 7:137442765 A 9162 NM_004717.2 Transcript intron_variant - - - - - - rs4732266 7:137442765 A ENSESTG00000029065 ENSESTT00000073255 Transcript intron_variant - - - - - - rs4732266 7:137442765 A ENSESTG00000029065 ENSESTT00000073200 Transcript intron_variant - - - - - - rs192438 7:137571505 T ENSESTG00000029009 ENSESTT00000073148 Transcript intron_variant - - - - - - rs192438 7:137571505 T 64764 NM_194071.3 Transcript intron_variant - - - - - - rs192438 7:137571505 T ENSESTG00000029009 ENSESTT00000073164 Transcript upstream_gene_variant - - - - - - DISTANCE=4130 rs192438 7:137571505 T CCDS34760.1 CCDS34760.1 Transcript intron_variant - - - - - - rs2352475 7:137884981 T - - - intergenic_variant - - - - - - rs10215073 7:137960080 T - - - intergenic_variant - - - - - - rs428078 7:138042308 G - - - intergenic_variant - - - - - - rs357395 7:138049370 T - - - intergenic_variant - - - - - - rs367339 7:138077768 A - - - intergenic_variant - - - - - - rs4728443 7:138355355 C 136306 NM_001139456.1 Transcript intron_variant - - - - - - rs4728443 7:138355355 C CCDS47721.1 CCDS47721.1 Transcript intron_variant - - - - - - rs4421309 7:138356584 G 136306 NM_001139456.1 Transcript intron_variant - - - - - - rs4421309 7:138356584 G CCDS47721.1 CCDS47721.1 Transcript intron_variant - - - - - - rs2774977 7:138649497 A CCDS47723.2 CCDS47723.2 Transcript intron_variant - - - - - - rs2774977 7:138649497 A CCDS56513.1 CCDS56513.1 Transcript intron_variant - - - - - - rs2774977 7:138649497 A 57670 NM_020910.2 Transcript intron_variant - - - - - - rs2774977 7:138649497 A 57670 NM_001164665.1 Transcript intron_variant - - - - - - rs144797979 7:141938760 T 100289017 NR_024346.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1796 rs145177459 7:141952896 A ENSESTG00000027201 ENSESTT00000068598 Transcript intron_variant - - - - - - rs145177459 7:141952896 A CCDS5871.1 CCDS5871.1 Transcript intron_variant - - - - - - rs145177459 7:141952896 A 136541 NM_001001317.3 Transcript intron_variant - - - - - - rs147221863 7:142010578 C 28617 NC_000007.13:TRBV4-1:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=2458 rs147221863 7:142010578 C 28619 NC_000007.13:TRBV3-1:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1707 rs138339752 7:142257750 G - ENSR00001564686 RegulatoryFeature regulatory_region_variant - - - - - - rs138339752 7:142257750 G 28613 NC_000007.13:TRBV5-2:u_t_1 Transcript downstream_gene_variant - - - - - - DISTANCE=1308 rs58562755 7:142598328 A ENSESTG00000032094 ENSESTT00000081001 Transcript intron_variant - - - - - - rs3113187 7:142808415 G - - - intergenic_variant - - - - - - rs10269527 7:143053260 G ENSESTG00000032180 ENSESTT00000081273 Transcript downstream_gene_variant - - - - - - DISTANCE=547 rs10269527 7:143053260 G 1180 NR_046453.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4163 rs10269527 7:143053260 G ENSESTG00000032180 ENSESTT00000081261 Transcript downstream_gene_variant - - - - - - DISTANCE=3506 rs10269527 7:143053260 G 1180 NM_000083.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4163 rs10269527 7:143053260 G ENSESTG00000032180 ENSESTT00000081305 Transcript downstream_gene_variant - - - - - - DISTANCE=547 rs10269527 7:143053260 G ENSESTG00000032180 ENSESTT00000081281 Transcript downstream_gene_variant - - - - - - DISTANCE=2659 rs10269527 7:143053260 G CCDS47734.1 CCDS47734.1 Transcript downstream_gene_variant - - - - - - DISTANCE=383 rs10269527 7:143053260 G ENSESTG00000032180 ENSESTT00000081300 Transcript downstream_gene_variant - - - - - - DISTANCE=547 rs10269527 7:143053260 G ENSESTG00000032180 ENSESTT00000081290 Transcript downstream_gene_variant - - - - - - DISTANCE=547 rs10269527 7:143053260 G 9715 NM_014690.4 Transcript 3_prime_UTR_variant 1503 - - - - - rs10269527 7:143053260 G ENSESTG00000032180 ENSESTT00000081254 Transcript downstream_gene_variant - - - - - - DISTANCE=547 rs10269527 7:143053260 G CCDS5881.1 CCDS5881.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4202 rs10269527 7:143053260 G CCDS5882.1 CCDS5882.1 Transcript downstream_gene_variant - - - - - - DISTANCE=383 rs10269527 7:143053260 G 9715 NM_001031690.2 Transcript 3_prime_UTR_variant 1610 - - - - - rs2966726 7:143149775 G - ENSR00000314317 RegulatoryFeature regulatory_region_variant - - - - - - rs2966726 7:143149775 G 285965 NR_033897.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1635333 7:144442746 T CCDS55178.1 CCDS55178.1 Transcript intron_variant - - - - - - rs1635333 7:144442746 T ENSESTG00000014922 ENSESTT00000037386 Transcript intron_variant - - - - - - rs1635333 7:144442746 T ENSESTG00000033748 ENSESTT00000085319 Transcript intron_variant - - - - - - rs1635333 7:144442746 T ENSESTG00000033748 ENSESTT00000085327 Transcript intron_variant - - - - - - rs1635333 7:144442746 T ENSESTG00000014922 ENSESTT00000037413 Transcript intron_variant - - - - - - rs1635333 7:144442746 T 27010 NM_022445.3 Transcript intron_variant - - - - - - rs1635333 7:144442746 T CCDS5888.1 CCDS5888.1 Transcript intron_variant - - - - - - rs1635333 7:144442746 T 27010 NM_001042482.1 Transcript intron_variant - - - - - - rs4726726 7:144658589 G - - - intergenic_variant - - - - - - rs1609235 7:145188794 A - - - intergenic_variant - - - - - - rs1523957 7:145292605 G - - - intergenic_variant - - - - - - rs1917654 7:145820599 G CCDS5889.1 CCDS5889.1 Transcript intron_variant - - - - - - rs1917654 7:145820599 G 26047 NM_014141.5 Transcript intron_variant - - - - - - rs802507 7:145971603 T CCDS5889.1 CCDS5889.1 Transcript intron_variant - - - - - - rs802507 7:145971603 T 26047 NM_014141.5 Transcript intron_variant - - - - - - rs12703833 7:146408100 C CCDS5889.1 CCDS5889.1 Transcript intron_variant - - - - - - rs12703833 7:146408100 C 26047 NM_014141.5 Transcript intron_variant - - - - - - rs1568783 7:146651570 A CCDS5889.1 CCDS5889.1 Transcript intron_variant - - - - - - rs1568783 7:146651570 A 26047 NM_014141.5 Transcript intron_variant - - - - - - rs1014685 7:146775421 T CCDS5889.1 CCDS5889.1 Transcript intron_variant - - - - - - rs1014685 7:146775421 T 26047 NM_014141.5 Transcript intron_variant - - - - - - rs1014685 7:146775421 T ENSESTG00000031833 ENSESTT00000080309 Transcript downstream_gene_variant - - - - - - DISTANCE=4658 rs1014685 7:146775421 T ENSESTG00000031792 ENSESTT00000080260 Transcript intron_variant - - - - - - rs826797 7:147032555 A CCDS5889.1 CCDS5889.1 Transcript intron_variant - - - - - - rs826797 7:147032555 A 26047 NM_014141.5 Transcript intron_variant - - - - - - rs826797 7:147032555 A ENSESTG00000031792 ENSESTT00000080260 Transcript intron_variant - - - - - - rs851822 7:147241130 G CCDS5889.1 CCDS5889.1 Transcript intron_variant - - - - - - rs851822 7:147241130 G 26047 NM_014141.5 Transcript intron_variant - - - - - - rs1101046 7:147403376 G CCDS5889.1 CCDS5889.1 Transcript intron_variant - - - - - - rs1101046 7:147403376 G 26047 NM_014141.5 Transcript intron_variant - - - - - - rs6961303 7:148142349 C - - - intergenic_variant - - - - - - rs6962100 7:150780933 G - ENSR00001565013 RegulatoryFeature regulatory_region_variant - - - - - - rs6962100 7:150780933 G 10922 NM_033015.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2963 rs6962100 7:150780933 G 10922 NM_006712.4 Transcript upstream_gene_variant - - - - - - DISTANCE=2963 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044183 Transcript upstream_gene_variant - - - - - - DISTANCE=1985 rs6962100 7:150780933 G CCDS5920.1 CCDS5920.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1283 rs6962100 7:150780933 G 116988 NM_001042535.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2893 rs6962100 7:150780933 G ENSESTG00000018532 ENSESTT00000046711 Transcript upstream_gene_variant - - - - - - DISTANCE=3050 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044296 Transcript upstream_gene_variant - - - - - - DISTANCE=2576 rs6962100 7:150780933 G CCDS5918.1 CCDS5918.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3080 rs6962100 7:150780933 G 116988 NM_031946.4 Transcript upstream_gene_variant - - - - - - DISTANCE=2893 rs6962100 7:150780933 G ENSESTG00000018532 ENSESTT00000046698 Transcript upstream_gene_variant - - - - - - DISTANCE=2982 rs6962100 7:150780933 G ENSESTG00000018532 ENSESTT00000046636 Transcript upstream_gene_variant - - - - - - DISTANCE=2972 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044232 Transcript upstream_gene_variant - - - - - - DISTANCE=2021 rs6962100 7:150780933 G 10922 NM_001258461.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2963 rs6962100 7:150780933 G 83590 NM_001136044.1 Transcript upstream_gene_variant - - - - - - DISTANCE=313 rs6962100 7:150780933 G CCDS5919.1 CCDS5919.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3080 rs6962100 7:150780933 G CCDS43681.1 CCDS43681.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2896 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044213 Transcript upstream_gene_variant - - - - - - DISTANCE=1985 rs6962100 7:150780933 G CCDS55185.1 CCDS55185.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2896 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044344 Transcript upstream_gene_variant - - - - - - DISTANCE=2896 rs6962100 7:150780933 G 83590 NM_031434.3 Transcript upstream_gene_variant - - - - - - DISTANCE=520 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044292 Transcript upstream_gene_variant - - - - - - DISTANCE=2576 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044226 Transcript upstream_gene_variant - - - - - - DISTANCE=2021 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044313 Transcript upstream_gene_variant - - - - - - DISTANCE=2629 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044338 Transcript upstream_gene_variant - - - - - - DISTANCE=2896 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044306 Transcript upstream_gene_variant - - - - - - DISTANCE=2629 rs6962100 7:150780933 G ENSESTG00000017513 ENSESTT00000044172 Transcript upstream_gene_variant - - - - - - DISTANCE=1985 rs6962100 7:150780933 G CCDS59088.1 CCDS59088.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3080 rs429124 7:151059891 C CCDS59089.1 CCDS59089.1 Transcript intron_variant - - - - - - rs429124 7:151059891 C 51667 NM_016118.4 Transcript intron_variant - - - - - - rs429124 7:151059891 C ENSESTG00000017714 ENSESTT00000044868 Transcript intron_variant - - - - - - rs429124 7:151059891 C ENSESTG00000017714 ENSESTT00000044876 Transcript downstream_gene_variant - - - - - - DISTANCE=2286 rs429124 7:151059891 C ENSESTG00000017714 ENSESTT00000044837 Transcript intron_variant - - - - - - rs429124 7:151059891 C CCDS47751.2 CCDS47751.2 Transcript intron_variant - - - - - - rs429124 7:151059891 C ENSESTG00000017714 ENSESTT00000044844 Transcript downstream_gene_variant - - - - - - DISTANCE=2286 rs429124 7:151059891 C ENSESTG00000017714 ENSESTT00000044860 Transcript intron_variant - - - - - - rs429124 7:151059891 C ENSESTG00000017714 ENSESTT00000044883 Transcript upstream_gene_variant - - - - - - DISTANCE=4129 rs429124 7:151059891 C 51667 NM_001243351.1 Transcript intron_variant - - - - - - rs429124 7:151059891 C ENSESTG00000017714 ENSESTT00000044833 Transcript intron_variant - - - - - - rs421975 7:151060301 T CCDS59089.1 CCDS59089.1 Transcript intron_variant - - - - - - rs421975 7:151060301 T 51667 NM_016118.4 Transcript intron_variant - - - - - - rs421975 7:151060301 T ENSESTG00000017714 ENSESTT00000044868 Transcript intron_variant - - - - - - rs421975 7:151060301 T ENSESTG00000017714 ENSESTT00000044876 Transcript downstream_gene_variant - - - - - - DISTANCE=2696 rs421975 7:151060301 T ENSESTG00000017714 ENSESTT00000044837 Transcript intron_variant - - - - - - rs421975 7:151060301 T CCDS47751.2 CCDS47751.2 Transcript intron_variant - - - - - - rs421975 7:151060301 T ENSESTG00000017714 ENSESTT00000044844 Transcript downstream_gene_variant - - - - - - DISTANCE=2696 rs421975 7:151060301 T ENSESTG00000017714 ENSESTT00000044860 Transcript intron_variant - - - - - - rs421975 7:151060301 T ENSESTG00000017714 ENSESTT00000044883 Transcript upstream_gene_variant - - - - - - DISTANCE=3719 rs421975 7:151060301 T 51667 NM_001243351.1 Transcript intron_variant - - - - - - rs421975 7:151060301 T ENSESTG00000017714 ENSESTT00000044833 Transcript intron_variant - - - - - - rs7781457 7:151619298 C - - - intergenic_variant - - - - - - rs10952358 7:152234992 A - - - intergenic_variant - - - - - - rs3111473 7:152366301 A 7516 NM_005431.1 Transcript intron_variant - - - - - - rs3111473 7:152366301 A ENSESTG00000007406 ENSESTT00000018654 Transcript intron_variant - - - - - - rs3111473 7:152366301 A CCDS5933.1 CCDS5933.1 Transcript intron_variant - - - - - - rs476008 7:152754865 T - - - intergenic_variant - - - - - - rs1199475 7:153069160 C - - - intergenic_variant - - - - - - rs4726322 7:153352544 A - - - intergenic_variant - - - - - - rs1239324 7:154753635 C CCDS47753.1 CCDS47753.1 Transcript intron_variant - - - - - - rs1239324 7:154753635 C ENSESTG00000035349 ENSESTT00000089257 Transcript intron_variant - - - - - - rs1239324 7:154753635 C 22976 NM_007349.3 Transcript intron_variant - - - - - - rs4398858 7:154780960 T CCDS47753.1 CCDS47753.1 Transcript intron_variant - - - - - - rs4398858 7:154780960 T ENSESTG00000035342 ENSESTT00000089234 Transcript intron_variant - - - - - - rs4398858 7:154780960 T ENSESTG00000035342 ENSESTT00000089236 Transcript upstream_gene_variant - - - - - - DISTANCE=1639 rs4398858 7:154780960 T 22976 NM_007349.3 Transcript intron_variant - - - - - - rs6597450 7:154835327 A - - - intergenic_variant - - - - - - rs4960688 7:154934269 A - - - intergenic_variant - - - - - - rs9690811 7:155073554 T - - - intergenic_variant - - - - - - rs9770063 7:155075549 G - ENSR00000636577 RegulatoryFeature regulatory_region_variant - - - - - - rs9770063 7:155075549 G ENSESTG00000035337 ENSESTT00000089222 Transcript downstream_gene_variant - - - - - - DISTANCE=4748 rs1861959 7:155282984 C ENSESTG00000010703 ENSESTT00000026796 Transcript intron_variant - - - - - - rs10215792 7:155455528 G - ENSR00000636646 RegulatoryFeature regulatory_region_variant - - - - - - rs10215792 7:155455528 G 155435 NM_053043.2 Transcript intron_variant - - - - - - rs10215792 7:155455528 G ENSESTG00000010646 ENSESTT00000026650 Transcript intron_variant - - - - - - rs10215792 7:155455528 G CCDS5941.2 CCDS5941.2 Transcript intron_variant - - - - - - rs7781949 7:155469492 A - ENSR00000636651 RegulatoryFeature regulatory_region_variant - - - - - - rs7781949 7:155469492 A 155435 NM_053043.2 Transcript intron_variant - - - - - - rs7781949 7:155469492 A ENSESTG00000010646 ENSESTT00000026650 Transcript intron_variant - - - - - - rs7781949 7:155469492 A CCDS5941.2 CCDS5941.2 Transcript intron_variant - - - - - - rs12533575 7:155555659 C - ENSR00001565253 RegulatoryFeature regulatory_region_variant - - - - - - rs12533575 7:155555659 C ENSESTG00000010673 ENSESTT00000026698 Transcript intron_variant - - - - - - rs12533575 7:155555659 C ENSESTG00000010673 ENSESTT00000026700 Transcript intron_variant - - - - - - rs12533575 7:155555659 C 155435 NM_053043.2 Transcript intron_variant - - - - - - rs12533575 7:155555659 C CCDS5941.2 CCDS5941.2 Transcript intron_variant - - - - - - rs7791548 7:155556125 G ENSESTG00000010673 ENSESTT00000026698 Transcript intron_variant - - - - - - rs7791548 7:155556125 G ENSESTG00000010673 ENSESTT00000026700 Transcript intron_variant - - - - - - rs7791548 7:155556125 G 155435 NM_053043.2 Transcript intron_variant - - - - - - rs7791548 7:155556125 G CCDS5941.2 CCDS5941.2 Transcript intron_variant - - - - - - rs6945595 7:155661245 C - - - intergenic_variant - - - - - - rs10255313 7:155789569 C - - - intergenic_variant - - - - - - rs4717038 7:156127124 C - - - intergenic_variant - - - - - - rs6949603 7:156226563 T 285889 NR_038232.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3920 rs849070 7:156413698 T ENSESTG00000001602 ENSESTT00000003856 Transcript intron_variant - - - - - - rs1263545 7:157403753 C 5799 NM_130842.2 Transcript intron_variant - - - - - - rs1263545 7:157403753 C ENSESTG00000021485 ENSESTT00000053898 Transcript intron_variant - - - - - - rs1263545 7:157403753 C CCDS5949.1 CCDS5949.1 Transcript intron_variant - - - - - - rs1263545 7:157403753 C CCDS5947.1 CCDS5947.1 Transcript intron_variant - - - - - - rs1263545 7:157403753 C 5799 NM_002847.3 Transcript intron_variant - - - - - - rs1263545 7:157403753 C CCDS5948.1 CCDS5948.1 Transcript intron_variant - - - - - - rs1263545 7:157403753 C ENSESTG00000021392 ENSESTT00000053675 Transcript upstream_gene_variant - - - - - - DISTANCE=2962 rs1263545 7:157403753 C 5799 NM_130843.2 Transcript intron_variant - - - - - - rs6974664 7:157813276 G 5799 NM_130842.2 Transcript intron_variant - - - - - - rs6974664 7:157813276 G CCDS5949.1 CCDS5949.1 Transcript intron_variant - - - - - - rs6974664 7:157813276 G CCDS5947.1 CCDS5947.1 Transcript intron_variant - - - - - - rs6974664 7:157813276 G ENSESTG00000021472 ENSESTT00000053833 Transcript intron_variant - - - - - - rs6974664 7:157813276 G ENSESTG00000021472 ENSESTT00000053854 Transcript intron_variant - - - - - - rs6974664 7:157813276 G 5799 NM_002847.3 Transcript intron_variant - - - - - - rs6974664 7:157813276 G CCDS5948.1 CCDS5948.1 Transcript intron_variant - - - - - - rs6974664 7:157813276 G 5799 NM_130843.2 Transcript intron_variant - - - - - - rs61239508 7:157897870 C 5799 NM_130842.2 Transcript intron_variant - - - - - - rs61239508 7:157897870 C CCDS5949.1 CCDS5949.1 Transcript intron_variant - - - - - - rs61239508 7:157897870 C CCDS5947.1 CCDS5947.1 Transcript intron_variant - - - - - - rs61239508 7:157897870 C ENSESTG00000021472 ENSESTT00000053833 Transcript intron_variant - - - - - - rs61239508 7:157897870 C ENSESTG00000021472 ENSESTT00000053854 Transcript intron_variant - - - - - - rs61239508 7:157897870 C 5799 NM_002847.3 Transcript intron_variant - - - - - - rs61239508 7:157897870 C CCDS5948.1 CCDS5948.1 Transcript intron_variant - - - - - - rs61239508 7:157897870 C 5799 NM_130843.2 Transcript intron_variant - - - - - - rs4909067 7:158121970 G 5799 NM_130842.2 Transcript intron_variant - - - - - - rs4909067 7:158121970 G CCDS5949.1 CCDS5949.1 Transcript intron_variant - - - - - - rs4909067 7:158121970 G CCDS5947.1 CCDS5947.1 Transcript intron_variant - - - - - - rs4909067 7:158121970 G ENSESTG00000021427 ENSESTT00000053811 Transcript intron_variant - - - - - - rs4909067 7:158121970 G ENSESTG00000021427 ENSESTT00000053791 Transcript intron_variant - - - - - - rs4909067 7:158121970 G 5799 NM_002847.3 Transcript intron_variant - - - - - - rs4909067 7:158121970 G CCDS5948.1 CCDS5948.1 Transcript intron_variant - - - - - - rs4909067 7:158121970 G 5799 NM_130843.2 Transcript intron_variant - - - - - - rs1189194 7:158551985 T ENSESTG00000019029 ENSESTT00000048078 Transcript intron_variant - - - - - - rs1189194 7:158551985 T ENSESTG00000019029 ENSESTT00000048085 Transcript intron_variant - - - - - - rs1189194 7:158551985 T ENSESTG00000019029 ENSESTT00000048059 Transcript intron_variant - - - - - - rs1189194 7:158551985 T 57488 NM_020728.2 Transcript intron_variant - - - - - - rs1189194 7:158551985 T ENSESTG00000019029 ENSESTT00000048039 Transcript intron_variant - - - - - - rs1189194 7:158551985 T CCDS34791.1 CCDS34791.1 Transcript intron_variant - - - - - - rs2730283 7:158876560 C ENSESTG00000018971 ENSESTT00000047719 Transcript intron_variant - - - - - - rs2730283 7:158876560 C ENSESTG00000018979 ENSESTT00000047796 Transcript intron_variant - - - - - - rs2730283 7:158876560 C 7434 NM_003382.4 Transcript intron_variant - - - - - - rs2730283 7:158876560 C ENSESTG00000018979 ENSESTT00000047821 Transcript intron_variant - - - - - - rs2730283 7:158876560 C CCDS5950.1 CCDS5950.1 Transcript intron_variant - - - - - - rs439204 7:158935333 C ENSESTG00000018979 ENSESTT00000047796 Transcript intron_variant - - - - - - rs439204 7:158935333 C 7434 NM_003382.4 Transcript intron_variant - - - - - - rs439204 7:158935333 C ENSESTG00000018979 ENSESTT00000047807 Transcript intron_variant - - - - - - rs439204 7:158935333 C CCDS5950.1 CCDS5950.1 Transcript intron_variant - - - - - - rs382552 7:158947185 G - ENSR00000683915 RegulatoryFeature regulatory_region_variant - - - - - - rs382552 7:158947185 G - - - intergenic_variant - - - - - - rs439544 7:158949771 C - - - intergenic_variant - - - - - - rs404996 7:158957888 A - - - intergenic_variant - - - - - - rs408870 7:158962161 G - - - intergenic_variant - - - - - - rs377424 7:158985310 G - - - intergenic_variant - - - - - - rs382468 7:158989758 T - ENSR00000315297 RegulatoryFeature regulatory_region_variant - - - - - - rs382468 7:158989758 T - - - intergenic_variant - - - - - - rs428383 7:159007173 T - - - intergenic_variant - - - - - - rs405600 7:159011073 A - - - intergenic_variant - - - - - - rs432245 7:159017931 C - - - intergenic_variant - - - - - - rs415892 7:159035511 C - - - intergenic_variant - - - - - - rs3976691 7:159062099 T - - - intergenic_variant - - - - - - rs6459932 7:159069598 T - - - intergenic_variant - - - - - - rs2205064 7:159081696 C - - - intergenic_variant - - - - - - rs4735846 8:434605 C ENSESTG00000005279 ENSESTT00000013439 Transcript downstream_gene_variant - - - - - - DISTANCE=1741 rs10110702 8:546124 C - - - intergenic_variant - - - - - - rs896521 8:617718 G ENSESTG00000005321 ENSESTT00000013576 Transcript intron_variant - - - - - - rs896521 8:617718 G ENSESTG00000005321 ENSESTT00000013571 Transcript intron_variant - - - - - - rs896521 8:617718 G CCDS5955.1 CCDS5955.1 Transcript intron_variant - - - - - - rs896521 8:617718 G 157697 NM_207332.1 Transcript intron_variant - - - - - - rs896521 8:617718 G ENSESTG00000005321 ENSESTT00000013529 Transcript downstream_gene_variant - - - - - - DISTANCE=879 rs6559200 8:948461 C ENSESTG00000005299 ENSESTT00000013502 Transcript intron_variant - - - - - - rs6559200 8:948461 C ENSESTG00000005299 ENSESTT00000013491 Transcript intron_variant - - - - - - rs7831705 8:999557 G ENSESTG00000005299 ENSESTT00000013502 Transcript intron_variant - - - - - - rs6559206 8:1002828 G ENSESTG00000005299 ENSESTT00000013502 Transcript intron_variant - - - - - - rs6559216 8:1045738 C ENSESTG00000005299 ENSESTT00000013502 Transcript intron_variant - - - - - - rs6558413 8:1069005 C ENSESTG00000005299 ENSESTT00000013502 Transcript intron_variant - - - - - - rs6558414 8:1074197 T ENSESTG00000005299 ENSESTT00000013502 Transcript intron_variant - - - - - - rs6982854 8:1260132 G - - - intergenic_variant - - - - - - rs6420197 8:1840084 A ENSESTG00000017766 ENSESTT00000045127 Transcript intron_variant - - - - - - rs6420197 8:1840084 A ENSESTG00000017766 ENSESTT00000045067 Transcript intron_variant - - - - - - rs6420197 8:1840084 A ENSESTG00000017766 ENSESTT00000045078 Transcript intron_variant - - - - - - rs6420197 8:1840084 A ENSESTG00000017766 ENSESTT00000045000 Transcript intron_variant - - - - - - rs6420197 8:1840084 A CCDS34794.1 CCDS34794.1 Transcript intron_variant - - - - - - rs6420197 8:1840084 A ENSESTG00000017766 ENSESTT00000045037 Transcript intron_variant - - - - - - rs6420197 8:1840084 A 9639 NM_014629.2 Transcript intron_variant - - - - - - rs6420197 8:1840084 A ENSESTG00000017766 ENSESTT00000045099 Transcript intron_variant - - - - - - rs2607708 8:2212361 G - ENSR00001384671 RegulatoryFeature regulatory_region_variant - - - - - - rs2607708 8:2212361 G - - - intergenic_variant - - - - - - rs1671785 8:2246343 T - - - intergenic_variant - - - - - - rs6558667 8:2426418 A - - - intergenic_variant - - - - - - rs11136526 8:2462734 A ENSESTG00000008424 ENSESTT00000021242 Transcript intron_variant - - - - - - rs11136526 8:2462734 A ENSESTG00000008424 ENSESTT00000021268 Transcript intron_variant - - - - - - rs4242528 8:2491077 A ENSESTG00000008424 ENSESTT00000021242 Transcript intron_variant - - - - - - rs341741 8:2782683 T - - - intergenic_variant - - - - - - rs620810 8:2889132 G CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs620810 8:2889132 G ENSESTG00000008391 ENSESTT00000021178 Transcript intron_variant - - - - - - rs620810 8:2889132 G 64478 NM_033225.5 Transcript intron_variant - - - - - - rs620810 8:2889132 G ENSESTG00000008391 ENSESTT00000021168 Transcript intron_variant - - - - - - rs259861 8:3039362 G CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs259861 8:3039362 G ENSESTG00000029547 ENSESTT00000074342 Transcript intron_variant - - - - - - rs259861 8:3039362 G 64478 NM_033225.5 Transcript intron_variant - - - - - - rs2440724 8:3064861 G ENSESTG00000029507 ENSESTT00000074306 Transcript intron_variant - - - - - - rs2440724 8:3064861 G CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs2440724 8:3064861 G ENSESTG00000029507 ENSESTT00000074293 Transcript intron_variant - - - - - - rs2440724 8:3064861 G 64478 NM_033225.5 Transcript intron_variant - - - - - - rs259852 8:3078941 G ENSESTG00000029507 ENSESTT00000074306 Transcript intron_variant - - - - - - rs259852 8:3078941 G CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs259852 8:3078941 G ENSESTG00000029507 ENSESTT00000074293 Transcript intron_variant - - - - - - rs259852 8:3078941 G 64478 NM_033225.5 Transcript intron_variant - - - - - - rs7846442 8:3104884 C - ENSR00001384755 RegulatoryFeature regulatory_region_variant - - - - - - rs7846442 8:3104884 C ENSESTG00000029507 ENSESTT00000074306 Transcript intron_variant - - - - - - rs7846442 8:3104884 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs7846442 8:3104884 C ENSESTG00000029507 ENSESTT00000074293 Transcript intron_variant - - - - - - rs7846442 8:3104884 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs7824604 8:3220658 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs7824604 8:3220658 C ENSESTG00000029447 ENSESTT00000074223 Transcript intron_variant - - - - - - rs7824604 8:3220658 C ENSESTG00000029447 ENSESTT00000074209 Transcript intron_variant - - - - - - rs7824604 8:3220658 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs7816584 8:3351558 A CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs7816584 8:3351558 A ENSESTG00000029429 ENSESTT00000074073 Transcript intron_variant - - - - - - rs7816584 8:3351558 A 64478 NM_033225.5 Transcript intron_variant - - - - - - rs2046220 8:3414373 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs2046220 8:3414373 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs6558822 8:3669957 T CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs6558822 8:3669957 T 64478 NM_033225.5 Transcript intron_variant - - - - - - rs1714779 8:4013549 A CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs1714779 8:4013549 A 64478 NM_033225.5 Transcript intron_variant - - - - - - rs2680614 8:4031589 C - ENSR00001384795 RegulatoryFeature regulatory_region_variant - - - - - - rs2680614 8:4031589 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs2680614 8:4031589 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs1714780 8:4041246 G CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs1714780 8:4041246 G 64478 NM_033225.5 Transcript intron_variant - - - - - - rs6981997 8:4169328 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs6981997 8:4169328 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs10102515 8:4177436 G CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs10102515 8:4177436 G 64478 NM_033225.5 Transcript intron_variant - - - - - - rs1154078 8:4330917 G CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs1154078 8:4330917 G 64478 NM_033225.5 Transcript intron_variant - - - - - - rs1658823 8:4340555 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs1658823 8:4340555 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs2118571 8:4624798 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs2118571 8:4624798 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs6982675 8:4628401 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs6982675 8:4628401 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs6558917 8:4629650 T CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs6558917 8:4629650 T 64478 NM_033225.5 Transcript intron_variant - - - - - - rs1840880 8:4638234 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs1840880 8:4638234 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs13252806 8:4762942 T CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs13252806 8:4762942 T 64478 NM_033225.5 Transcript intron_variant - - - - - - rs6982354 8:4786273 G CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs6982354 8:4786273 G 64478 NM_033225.5 Transcript intron_variant - - - - - - rs7014153 8:4792633 G CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs7014153 8:4792633 G 64478 NM_033225.5 Transcript intron_variant - - - - - - rs4273871 8:4795667 C CCDS55189.1 CCDS55189.1 Transcript intron_variant - - - - - - rs4273871 8:4795667 C 64478 NM_033225.5 Transcript intron_variant - - - - - - rs12545180 8:5021883 G - - - intergenic_variant - - - - - - rs13265033 8:5227297 C - - - intergenic_variant - - - - - - rs2006471 8:5230251 A - - - intergenic_variant - - - - - - rs2111422 8:5255364 A - - - intergenic_variant - - - - - - rs7015358 8:5256899 G - - - intergenic_variant - - - - - - rs4639536 8:5287953 G - - - intergenic_variant - - - - - - rs2733079 8:5445343 G - - - intergenic_variant - - - - - - rs2527723 8:5468489 C - - - intergenic_variant - - - - - - rs4367572 8:5626408 G - - - intergenic_variant - - - - - - rs2916697 8:6218668 A - - - intergenic_variant - - - - - - rs3098003 8:6223757 A - - - intergenic_variant - - - - - - rs2515544 8:6458667 C ENSESTG00000023289 ENSESTT00000058840 Transcript intron_variant - - - - - - rs2515544 8:6458667 C ENSESTG00000023289 ENSESTT00000058861 Transcript intron_variant - - - - - - rs2515544 8:6458667 C ENSESTG00000023289 ENSESTT00000058830 Transcript intron_variant - - - - - - rs2515544 8:6458667 C CCDS43689.1 CCDS43689.1 Transcript intron_variant - - - - - - rs2515544 8:6458667 C ENSESTG00000023289 ENSESTT00000058892 Transcript intron_variant - - - - - - rs2515544 8:6458667 C ENSESTG00000023289 ENSESTT00000058866 Transcript intron_variant - - - - - - rs2515544 8:6458667 C 79648 NM_024596.3 Transcript intron_variant - - - - - - rs2980660 8:6477478 C - ENSR00001384953 RegulatoryFeature regulatory_region_variant - - - - - - rs2980660 8:6477478 C ENSESTG00000023289 ENSESTT00000058840 Transcript intron_variant - - - - - - rs2980660 8:6477478 C ENSESTG00000023289 ENSESTT00000058861 Transcript intron_variant - - - - - - rs2980660 8:6477478 C ENSESTG00000023289 ENSESTT00000058830 Transcript intron_variant - - - - - - rs2980660 8:6477478 C CCDS43689.1 CCDS43689.1 Transcript intron_variant - - - - - - rs2980660 8:6477478 C ENSESTG00000023289 ENSESTT00000058892 Transcript intron_variant - - - - - - rs2980660 8:6477478 C ENSESTG00000023289 ENSESTT00000058866 Transcript intron_variant - - - - - - rs2980660 8:6477478 C 79648 NM_024596.3 Transcript intron_variant - - - - - - rs2912055 8:6481284 C ENSESTG00000023289 ENSESTT00000058840 Transcript intron_variant - - - - - - rs2912055 8:6481284 C ENSESTG00000023289 ENSESTT00000058861 Transcript intron_variant - - - - - - rs2912055 8:6481284 C ENSESTG00000023289 ENSESTT00000058830 Transcript intron_variant - - - - - - rs2912055 8:6481284 C CCDS43689.1 CCDS43689.1 Transcript intron_variant - - - - - - rs2912055 8:6481284 C ENSESTG00000023289 ENSESTT00000058892 Transcript intron_variant - - - - - - rs2912055 8:6481284 C ENSESTG00000023289 ENSESTT00000058866 Transcript intron_variant - - - - - - rs2912055 8:6481284 C 79648 NM_024596.3 Transcript intron_variant - - - - - - rs2912008 8:6520567 G - - - intergenic_variant - - - - - - rs2980695 8:6557609 A - ENSR00001384967 RegulatoryFeature regulatory_region_variant - - - - - - rs2980695 8:6557609 A - - - intergenic_variant - - - - - - rs2980681 8:6588890 A ENSESTG00000023368 ENSESTT00000059106 Transcript intron_variant - - - - - - rs2980681 8:6588890 A 55326 NM_018361.3 Transcript intron_variant - - - - - - rs2980681 8:6588890 A CCDS34796.1 CCDS34796.1 Transcript intron_variant - - - - - - rs2980681 8:6588890 A ENSESTG00000023368 ENSESTT00000059122 Transcript downstream_gene_variant - - - - - - DISTANCE=599 rs2980681 8:6588890 A ENSESTG00000023368 ENSESTT00000059074 Transcript intron_variant - - - - - - rs2978942 8:6630460 C - - - intergenic_variant - - - - - - rs2928598 8:6630571 G - - - intergenic_variant - - - - - - rs2912033 8:6633176 G - - - intergenic_variant - - - - - - rs2912021 8:6642558 C - - - intergenic_variant - - - - - - rs2912014 8:6651255 C - - - intergenic_variant - - - - - - rs2912079 8:6652150 C - ENSR00001385000 RegulatoryFeature regulatory_region_variant - - - - - - rs2912079 8:6652150 C - - - intergenic_variant - - - - - - rs2977774 8:6731776 C 1672 NM_005218.3 Transcript intron_variant - - - - - - rs2977774 8:6731776 C ENSESTG00000023472 ENSESTT00000059174 Transcript intron_variant - - - - - - rs2977774 8:6731776 C CCDS5959.1 CCDS5959.1 Transcript intron_variant - - - - - - rs2977774 8:6731776 C ENSESTG00000023625 ENSESTT00000059612 Transcript intron_variant - - - - - - rs2977829 8:6736073 C 1672 NM_005218.3 Transcript upstream_gene_variant - - - - - - DISTANCE=544 rs2977829 8:6736073 C ENSESTG00000023472 ENSESTT00000059174 Transcript intron_variant - - - - - - rs2977829 8:6736073 C CCDS5959.1 CCDS5959.1 Transcript upstream_gene_variant - - - - - - DISTANCE=694 rs2977829 8:6736073 C ENSESTG00000023625 ENSESTT00000059612 Transcript upstream_gene_variant - - - - - - DISTANCE=583 rs4481622 8:6882477 T - - - intergenic_variant - - - - - - rs4332158 8:6882810 T - - - intergenic_variant - - - - - - rs4840665 8:6883855 G - - - intergenic_variant - - - - - - rs7821152 8:6886855 T - - - intergenic_variant - - - - - - rs4342632 8:6896572 C - - - intergenic_variant - - - - - - rs4601339 8:6896832 T - - - intergenic_variant - - - - - - rs2978719 8:6923466 C ENSESTG00000023491 ENSESTT00000059223 Transcript intron_variant - - - - - - rs809424 8:8102438 C - ENSR00001385241 RegulatoryFeature regulatory_region_variant - - - - - - rs809424 8:8102438 C 286042 NR_024363.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4886 rs809424 8:8102438 C 286042 NR_024361.1 Transcript downstream_gene_variant - - - - - - DISTANCE=51 rs2976838 8:8253445 G - - - intergenic_variant - - - - - - rs10110942 8:8287281 G - ENSR00001438702 RegulatoryFeature regulatory_region_variant - - - - - - rs10110942 8:8287281 G - - - intergenic_variant - - - - - - rs1703984 8:8557768 T CCDS55195.1 CCDS55195.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2141 rs1703984 8:8557768 T 137075 NM_194284.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1898 rs231187 8:8758397 C - - - intergenic_variant - - - - - - rs2100023 8:8871113 A - ENSR00001385470 RegulatoryFeature regulatory_region_variant - - - - - - rs2100023 8:8871113 A ENSESTG00000010969 ENSESTT00000027516 Transcript intron_variant - - - - - - rs2100023 8:8871113 A ENSESTG00000010969 ENSESTT00000027496 Transcript intron_variant - - - - - - rs2100023 8:8871113 A ENSESTG00000010969 ENSESTT00000027492 Transcript intron_variant - - - - - - rs2100023 8:8871113 A ENSESTG00000010969 ENSESTT00000027507 Transcript intron_variant - - - - - - rs2100023 8:8871113 A CCDS5972.1 CCDS5972.1 Transcript intron_variant - - - - - - rs2100023 8:8871113 A 90459 NM_153332.3 Transcript intron_variant - - - - - - rs2100023 8:8871113 A ENSESTG00000010969 ENSESTT00000027514 Transcript intron_variant - - - - - - rs2100023 8:8871113 A ENSESTG00000010969 ENSESTT00000027500 Transcript intron_variant - - - - - - rs2979251 8:8952778 A ENSESTG00000010969 ENSESTT00000027514 Transcript intron_variant - - - - - - rs2979251 8:8952778 A ENSESTG00000010969 ENSESTT00000027500 Transcript intron_variant - - - - - - rs2979251 8:8952778 A ENSESTG00000010969 ENSESTT00000027492 Transcript intron_variant - - - - - - rs6999534 8:8959611 G ENSESTG00000010969 ENSESTT00000027514 Transcript intron_variant - - - - - - rs6999534 8:8959611 G ENSESTG00000010969 ENSESTT00000027500 Transcript intron_variant - - - - - - rs6999534 8:8959611 G ENSESTG00000010969 ENSESTT00000027492 Transcript intron_variant - - - - - - rs7013401 8:8967918 C ENSESTG00000010969 ENSESTT00000027514 Transcript intron_variant - - - - - - rs7013401 8:8967918 C ENSESTG00000010969 ENSESTT00000027500 Transcript intron_variant - - - - - - rs7013401 8:8967918 C ENSESTG00000010969 ENSESTT00000027492 Transcript intron_variant - - - - - - rs7002141 8:9559985 T ENSESTG00000019810 ENSESTT00000049730 Transcript intron_variant - - - - - - rs7002141 8:9559985 T CCDS5974.1 CCDS5974.1 Transcript intron_variant - - - - - - rs7002141 8:9559985 T ENSESTG00000019810 ENSESTT00000049837 Transcript intron_variant - - - - - - rs7002141 8:9559985 T ENSESTG00000019810 ENSESTT00000049810 Transcript intron_variant - - - - - - rs7002141 8:9559985 T 8658 NM_003747.2 Transcript intron_variant - - - - - - rs7002141 8:9559985 T ENSESTG00000019810 ENSESTT00000049835 Transcript intron_variant - - - - - - rs7002141 8:9559985 T ENSESTG00000019810 ENSESTT00000049741 Transcript intron_variant - - - - - - rs13255492 8:9663442 C - - - intergenic_variant - - - - - - rs4840443 8:9679140 G - - - intergenic_variant - - - - - - rs560234 8:9831557 G - - - intergenic_variant - - - - - - rs628846 8:9837143 T - - - intergenic_variant - - - - - - rs535311 8:9839949 T - - - intergenic_variant - - - - - - rs546391 8:9848186 G - - - intergenic_variant - - - - - - rs628706 8:9855277 G - ENSR00001438820 RegulatoryFeature regulatory_region_variant - - - - - - rs628706 8:9855277 G - - - intergenic_variant - - - - - - rs630077 8:9855598 T - - - intergenic_variant - - - - - - rs544981 8:9860165 T - - - intergenic_variant - - - - - - rs1876512 8:9879722 C - - - intergenic_variant - - - - - - rs688469 8:9884798 T - - - intergenic_variant - - - - - - rs546142 8:9895042 C - - - intergenic_variant - - - - - - rs633961 8:9899724 C - - - intergenic_variant - - - - - - rs645503 8:9900001 G - - - intergenic_variant - - - - - - rs645542 8:9900025 G - - - intergenic_variant - - - - - - rs553820 8:9902184 C - - - intergenic_variant - - - - - - rs616069 8:9906455 A - - - intergenic_variant - - - - - - rs516067 8:9907035 T CCDS5975.1 CCDS5975.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4992 rs516067 8:9907035 T ENSESTG00000019942 ENSESTT00000050086 Transcript upstream_gene_variant - - - - - - DISTANCE=4829 rs516067 8:9907035 T ENSESTG00000019942 ENSESTT00000050072 Transcript upstream_gene_variant - - - - - - DISTANCE=4784 rs516067 8:9907035 T CCDS47798.1 CCDS47798.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4992 rs516067 8:9907035 T 4482 NM_012331.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4795 rs516067 8:9907035 T 4482 NM_001135670.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4795 rs3102552 8:9913357 G CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs3102552 8:9913357 G ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs3102552 8:9913357 G ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs3102552 8:9913357 G CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs3102552 8:9913357 G 4482 NM_012331.3 Transcript intron_variant - - - - - - rs3102552 8:9913357 G 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs626158 8:9914097 G CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs626158 8:9914097 G ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs626158 8:9914097 G ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs626158 8:9914097 G CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs626158 8:9914097 G 4482 NM_012331.3 Transcript intron_variant - - - - - - rs626158 8:9914097 G 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs814425 8:9914649 C CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs814425 8:9914649 C ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs814425 8:9914649 C ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs814425 8:9914649 C CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs814425 8:9914649 C 4482 NM_012331.3 Transcript intron_variant - - - - - - rs814425 8:9914649 C 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs640792 8:9915069 C - ENSR00001438822 RegulatoryFeature regulatory_region_variant - - - - - - rs640792 8:9915069 C CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs640792 8:9915069 C ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs640792 8:9915069 C ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs640792 8:9915069 C CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs640792 8:9915069 C 4482 NM_012331.3 Transcript intron_variant - - - - - - rs640792 8:9915069 C 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs497643 8:9917322 A CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs497643 8:9917322 A ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs497643 8:9917322 A ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs497643 8:9917322 A CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs497643 8:9917322 A 4482 NM_012331.3 Transcript intron_variant - - - - - - rs497643 8:9917322 A 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs476725 8:9920175 C CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs476725 8:9920175 C ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs476725 8:9920175 C ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs476725 8:9920175 C CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs476725 8:9920175 C 4482 NM_012331.3 Transcript intron_variant - - - - - - rs476725 8:9920175 C 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs2661752 8:9922281 C CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs2661752 8:9922281 C ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs2661752 8:9922281 C ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs2661752 8:9922281 C CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs2661752 8:9922281 C 4482 NM_012331.3 Transcript intron_variant - - - - - - rs2661752 8:9922281 C 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs814407 8:9929532 C CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs814407 8:9929532 C ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs814407 8:9929532 C ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs814407 8:9929532 C CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs814407 8:9929532 C 4482 NM_012331.3 Transcript intron_variant - - - - - - rs814407 8:9929532 C 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs2628144 8:9931415 C CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs2628144 8:9931415 C ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs2628144 8:9931415 C ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs2628144 8:9931415 C CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs2628144 8:9931415 C 4482 NM_012331.3 Transcript intron_variant - - - - - - rs2628144 8:9931415 C 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs814410 8:9933793 G CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs814410 8:9933793 G ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs814410 8:9933793 G ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs814410 8:9933793 G CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs814410 8:9933793 G 4482 NM_012331.3 Transcript intron_variant - - - - - - rs814410 8:9933793 G 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs814413 8:9935541 C CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs814413 8:9935541 C ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs814413 8:9935541 C ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs814413 8:9935541 C CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs814413 8:9935541 C 4482 NM_012331.3 Transcript intron_variant - - - - - - rs814413 8:9935541 C 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs6601433 8:10176218 C ENSESTG00000023262 ENSESTT00000058765 Transcript intron_variant - - - - - - rs6601433 8:10176218 C ENSESTG00000023262 ENSESTT00000058749 Transcript intron_variant - - - - - - rs6601433 8:10176218 C CCDS56522.1 CCDS56522.1 Transcript intron_variant - - - - - - rs6601433 8:10176218 C ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs6601433 8:10176218 C CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs6601433 8:10176218 C 4482 NM_012331.3 Transcript intron_variant - - - - - - rs6601433 8:10176218 C 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs6601433 8:10176218 C 4482 NM_001135671.1 Transcript intron_variant - - - - - - rs6601433 8:10176218 C CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs6601433 8:10176218 C 4482 NM_001199729.1 Transcript intron_variant - - - - - - rs6601433 8:10176218 C ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs6601433 8:10176218 C CCDS47799.1 CCDS47799.1 Transcript intron_variant - - - - - - rs6601435 8:10176300 C ENSESTG00000023262 ENSESTT00000058765 Transcript intron_variant - - - - - - rs6601435 8:10176300 C ENSESTG00000023262 ENSESTT00000058749 Transcript intron_variant - - - - - - rs6601435 8:10176300 C CCDS56522.1 CCDS56522.1 Transcript intron_variant - - - - - - rs6601435 8:10176300 C ENSESTG00000019942 ENSESTT00000050072 Transcript intron_variant - - - - - - rs6601435 8:10176300 C CCDS47798.1 CCDS47798.1 Transcript intron_variant - - - - - - rs6601435 8:10176300 C 4482 NM_012331.3 Transcript intron_variant - - - - - - rs6601435 8:10176300 C 4482 NM_001135670.1 Transcript intron_variant - - - - - - rs6601435 8:10176300 C 4482 NM_001135671.1 Transcript intron_variant - - - - - - rs6601435 8:10176300 C CCDS5975.1 CCDS5975.1 Transcript intron_variant - - - - - - rs6601435 8:10176300 C 4482 NM_001199729.1 Transcript intron_variant - - - - - - rs6601435 8:10176300 C ENSESTG00000019942 ENSESTT00000050086 Transcript intron_variant - - - - - - rs6601435 8:10176300 C CCDS47799.1 CCDS47799.1 Transcript intron_variant - - - - - - rs6601470 8:10347913 T - - - intergenic_variant - - - - - - rs4841378 8:10416053 C 203074 NM_001197020.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4377 rs4841378 8:10416053 C CCDS56523.1 CCDS56523.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4511 rs4349950 8:10425478 G - - - intergenic_variant - - - - - - rs4374952 8:10527820 C ENSESTG00000023347 ENSESTT00000058916 Transcript upstream_gene_variant - - - - - - DISTANCE=2343 rs4374952 8:10527820 C 203076 NM_001040032.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2327 rs4374952 8:10527820 C 100422982 NR_036248.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3240 rs4374952 8:10527820 C ENSESTG00000023347 ENSESTT00000058898 Transcript upstream_gene_variant - - - - - - DISTANCE=2328 rs4374952 8:10527820 C CCDS47800.1 CCDS47800.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2356 rs4374952 8:10527820 C ENSESTG00000023347 ENSESTT00000058921 Transcript upstream_gene_variant - - - - - - DISTANCE=2343 rs4374952 8:10527820 C ENSESTG00000023347 ENSESTT00000058931 Transcript upstream_gene_variant - - - - - - DISTANCE=4498 rs6601539 8:10804412 C CCDS5978.2 CCDS5978.2 Transcript intron_variant - - - - - - rs6601539 8:10804412 C 286046 NM_173683.3 Transcript intron_variant - - - - - - rs4266611 8:10856387 T CCDS5978.2 CCDS5978.2 Transcript intron_variant - - - - - - rs4266611 8:10856387 T 286046 NM_173683.3 Transcript intron_variant - - - - - - rs2898262 8:10964445 C ENSESTG00000019946 ENSESTT00000050010 Transcript downstream_gene_variant - - - - - - DISTANCE=4719 rs2898262 8:10964445 C CCDS5978.2 CCDS5978.2 Transcript intron_variant - - - - - - rs2898262 8:10964445 C 100996519 XM_003846380.1 Transcript downstream_gene_variant - - - - - - DISTANCE=853 rs2898262 8:10964445 C 286046 NM_173683.3 Transcript intron_variant - - - - - - rs11784661 8:11313339 G ENSESTG00000019858 ENSESTT00000049761 Transcript intron_variant - - - - - - rs11784661 8:11313339 G ENSESTG00000019858 ENSESTT00000049811 Transcript intron_variant - - - - - - rs11784661 8:11313339 G ENSESTG00000019858 ENSESTT00000049794 Transcript intron_variant - - - - - - rs11784661 8:11313339 G 83648 NM_053279.2 Transcript intron_variant - - - - - - rs2618477 8:11357635 C ENSESTG00000019940 ENSESTT00000049979 Transcript intron_variant - - - - - - rs2618477 8:11357635 C ENSESTG00000019462 ENSESTT00000049101 Transcript intron_variant - - - - - - rs2618477 8:11357635 C ENSESTG00000019462 ENSESTT00000049083 Transcript intron_variant - - - - - - rs2618477 8:11357635 C ENSESTG00000019462 ENSESTT00000049067 Transcript intron_variant - - - - - - rs2618477 8:11357635 C ENSESTG00000019462 ENSESTT00000049114 Transcript intron_variant - - - - - - rs2618477 8:11357635 C 640 NM_001715.2 Transcript intron_variant - - - - - - rs2467518 8:11416122 C - ENSR00001385938 RegulatoryFeature regulatory_region_variant - - - - - - rs2467518 8:11416122 C ENSESTG00000019940 ENSESTT00000049979 Transcript intron_variant - - - - - - rs2467518 8:11416122 C ENSESTG00000019462 ENSESTT00000049083 Transcript intron_variant - - - - - - rs2467518 8:11416122 C ENSESTG00000019462 ENSESTT00000049067 Transcript intron_variant - - - - - - rs2467518 8:11416122 C ENSESTG00000019462 ENSESTT00000049152 Transcript intron_variant - - - - - - rs2467518 8:11416122 C 640 NM_001715.2 Transcript intron_variant - - - - - - rs2467518 8:11416122 C ENSESTG00000019462 ENSESTT00000049170 Transcript upstream_gene_variant - - - - - - DISTANCE=4302 rs2467518 8:11416122 C ENSESTG00000019462 ENSESTT00000049151 Transcript intron_variant - - - - - - rs2467518 8:11416122 C CCDS5982.1 CCDS5982.1 Transcript intron_variant - - - - - - rs1390949 8:11729715 C 1508 NM_147782.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4069 rs1390949 8:11729715 C ENSESTG00000019890 ENSESTT00000049923 Transcript upstream_gene_variant - - - - - - DISTANCE=3522 rs1390949 8:11729715 C 1508 NM_001908.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4069 rs1390949 8:11729715 C 1508 NM_147780.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4069 rs1390949 8:11729715 C ENSESTG00000019890 ENSESTT00000049955 Transcript upstream_gene_variant - - - - - - DISTANCE=4117 rs1390949 8:11729715 C 1508 NM_147781.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4069 rs1390949 8:11729715 C ENSESTG00000019890 ENSESTT00000049861 Transcript upstream_gene_variant - - - - - - DISTANCE=3467 rs1390949 8:11729715 C ENSESTG00000019890 ENSESTT00000049882 Transcript upstream_gene_variant - - - - - - DISTANCE=3471 rs1390949 8:11729715 C ENSESTG00000019890 ENSESTT00000049962 Transcript upstream_gene_variant - - - - - - DISTANCE=4208 rs1390949 8:11729715 C 1508 NM_147783.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4069 rs1390949 8:11729715 C ENSESTG00000019890 ENSESTT00000049901 Transcript upstream_gene_variant - - - - - - DISTANCE=3493 rs142018514 8:12242981 G ENSESTG00000004867 ENSESTT00000012340 Transcript upstream_gene_variant - - - - - - DISTANCE=2291 rs142018514 8:12242981 G 100133172 NR_026789.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2977169 8:12734608 C - - - intergenic_variant - - - - - - rs2977154 8:12749727 G - - - intergenic_variant - - - - - - rs2977109 8:12759329 C - ENSR00001439003 RegulatoryFeature regulatory_region_variant - - - - - - rs2977109 8:12759329 C - - - intergenic_variant - - - - - - rs2956764 8:12768600 T - - - intergenic_variant - - - - - - rs2947400 8:12802772 G - ENSR00001439006 RegulatoryFeature regulatory_region_variant - - - - - - rs2947400 8:12802772 G 57604 NM_020844.2 Transcript upstream_gene_variant - - - - - - DISTANCE=411 rs2947400 8:12802772 G ENSESTG00000004880 ENSESTT00000012375 Transcript upstream_gene_variant - - - - - - DISTANCE=411 rs2947400 8:12802772 G ENSESTG00000004880 ENSESTT00000012379 Transcript upstream_gene_variant - - - - - - DISTANCE=551 rs2460348 8:12832790 G 57604 NM_020844.2 Transcript intron_variant - - - - - - rs2460348 8:12832790 G ENSESTG00000004880 ENSESTT00000012375 Transcript intron_variant - - - - - - rs2460348 8:12832790 G ENSESTG00000004880 ENSESTT00000012383 Transcript intron_variant - - - - - - rs2460348 8:12832790 G ENSESTG00000004880 ENSESTT00000012394 Transcript intron_variant - - - - - - rs2460348 8:12832790 G ENSESTG00000004880 ENSESTT00000012379 Transcript intron_variant - - - - - - rs2947394 8:12867404 C CCDS47808.1 CCDS47808.1 Transcript intron_variant - - - - - - rs2947394 8:12867404 C 57604 NM_020844.2 Transcript intron_variant - - - - - - rs2947394 8:12867404 C 57604 NM_001099677.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2369 rs2947394 8:12867404 C ENSESTG00000004880 ENSESTT00000012383 Transcript downstream_gene_variant - - - - - - DISTANCE=3662 rs2947394 8:12867404 C ENSESTG00000004880 ENSESTT00000012394 Transcript downstream_gene_variant - - - - - - DISTANCE=3636 rs2947394 8:12867404 C ENSESTG00000004880 ENSESTT00000012379 Transcript intron_variant - - - - - - rs477294 8:12953302 C CCDS5989.1 CCDS5989.1 Transcript intron_variant - - - - - - rs477294 8:12953302 C ENSESTG00000014813 ENSESTT00000037123 Transcript downstream_gene_variant - - - - - - DISTANCE=4767 rs477294 8:12953302 C ENSESTG00000014813 ENSESTT00000037158 Transcript downstream_gene_variant - - - - - - DISTANCE=4842 rs477294 8:12953302 C CCDS55201.1 CCDS55201.1 Transcript intron_variant - - - - - - rs477294 8:12953302 C 10395 NM_001164271.1 Transcript intron_variant - - - - - - rs477294 8:12953302 C 10395 NM_006094.4 Transcript intron_variant - - - - - - rs477294 8:12953302 C ENSESTG00000014813 ENSESTT00000037106 Transcript downstream_gene_variant - - - - - - DISTANCE=4653 rs477294 8:12953302 C CCDS5990.1 CCDS5990.1 Transcript intron_variant - - - - - - rs477294 8:12953302 C 10395 NM_182643.2 Transcript intron_variant - - - - - - rs477294 8:12953302 C ENSESTG00000014813 ENSESTT00000037163 Transcript downstream_gene_variant - - - - - - DISTANCE=4925 rs477294 8:12953302 C ENSESTG00000014813 ENSESTT00000037120 Transcript downstream_gene_variant - - - - - - DISTANCE=4778 rs1671336 8:13205173 T ENSESTG00000014813 ENSESTT00000037097 Transcript intron_variant - - - - - - rs1671336 8:13205173 T CCDS5989.1 CCDS5989.1 Transcript intron_variant - - - - - - rs1671336 8:13205173 T 10395 NM_024767.3 Transcript intron_variant - - - - - - rs1671336 8:13205173 T 10395 NM_182643.2 Transcript intron_variant - - - - - - rs1671336 8:13205173 T CCDS5991.2 CCDS5991.2 Transcript intron_variant - - - - - - rs1671427 8:13217693 C ENSESTG00000014813 ENSESTT00000037097 Transcript intron_variant - - - - - - rs1671427 8:13217693 C CCDS5989.1 CCDS5989.1 Transcript intron_variant - - - - - - rs1671427 8:13217693 C 10395 NM_024767.3 Transcript intron_variant - - - - - - rs1671427 8:13217693 C 10395 NM_182643.2 Transcript intron_variant - - - - - - rs1671427 8:13217693 C CCDS5991.2 CCDS5991.2 Transcript intron_variant - - - - - - rs7827060 8:13354245 A - ENSR00001386372 RegulatoryFeature regulatory_region_variant - - - - - - rs7827060 8:13354245 A CCDS5989.1 CCDS5989.1 Transcript intron_variant - - - - - - rs7827060 8:13354245 A 10395 NM_024767.3 Transcript intron_variant - - - - - - rs7827060 8:13354245 A 10395 NM_182643.2 Transcript intron_variant - - - - - - rs7827060 8:13354245 A CCDS5991.2 CCDS5991.2 Transcript intron_variant - - - - - - rs7827060 8:13354245 A ENSESTG00000014798 ENSESTT00000037060 Transcript downstream_gene_variant - - - - - - DISTANCE=2931 rs1383877 8:13457570 C ENSESTG00000014798 ENSESTT00000037060 Transcript intron_variant - - - - - - rs10087816 8:13467519 C - - - intergenic_variant - - - - - - rs6530656 8:13473228 G - - - intergenic_variant - - - - - - rs7001935 8:13589248 C - - - intergenic_variant - - - - - - rs6989020 8:13589512 C - - - intergenic_variant - - - - - - rs3853085 8:13916699 C - - - intergenic_variant - - - - - - rs1478033 8:13927454 C - - - intergenic_variant - - - - - - rs6530720 8:13933563 A - - - intergenic_variant - - - - - - rs6530721 8:13943499 G 137868 NM_139167.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3874 rs6530721 8:13943499 G CCDS5992.2 CCDS5992.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4453 rs6980825 8:14120004 G 137868 NM_139167.2 Transcript intron_variant - - - - - - rs6980825 8:14120004 G CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs1426994 8:14204047 A 137868 NM_139167.2 Transcript intron_variant - - - - - - rs1426994 8:14204047 A CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs1461874 8:14315542 A 137868 NM_139167.2 Transcript intron_variant - - - - - - rs1461874 8:14315542 A CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs3985616 8:14339311 G 137868 NM_139167.2 Transcript intron_variant - - - - - - rs3985616 8:14339311 G CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs1531423 8:14342394 T 137868 NM_139167.2 Transcript intron_variant - - - - - - rs1531423 8:14342394 T CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs6989351 8:14344038 A 137868 NM_139167.2 Transcript intron_variant - - - - - - rs6989351 8:14344038 A CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs6988078 8:14346749 C 137868 NM_139167.2 Transcript intron_variant - - - - - - rs6988078 8:14346749 C CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs7009025 8:14349329 G 137868 NM_139167.2 Transcript intron_variant - - - - - - rs7009025 8:14349329 G CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs6994616 8:14350230 G 137868 NM_139167.2 Transcript intron_variant - - - - - - rs6994616 8:14350230 G CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs7834116 8:14352308 A 137868 NM_139167.2 Transcript intron_variant - - - - - - rs7834116 8:14352308 A CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs1350871 8:14354069 T 137868 NM_139167.2 Transcript intron_variant - - - - - - rs1350871 8:14354069 T CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs1381415 8:14354239 T 137868 NM_139167.2 Transcript intron_variant - - - - - - rs1381415 8:14354239 T CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs7015187 8:14354331 A 137868 NM_139167.2 Transcript intron_variant - - - - - - rs7015187 8:14354331 A CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs898829 8:14366174 T 137868 NM_139167.2 Transcript intron_variant - - - - - - rs898829 8:14366174 T CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs1461877 8:14367033 T 137868 NM_139167.2 Transcript intron_variant - - - - - - rs1461877 8:14367033 T CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs2054358 8:14369833 A 137868 NM_139167.2 Transcript intron_variant - - - - - - rs2054358 8:14369833 A CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs10094262 8:14370332 C 137868 NM_139167.2 Transcript intron_variant - - - - - - rs10094262 8:14370332 C CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs2169425 8:14374699 T 137868 NM_139167.2 Transcript intron_variant - - - - - - rs2169425 8:14374699 T CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs2126326 8:14374955 A 137868 NM_139167.2 Transcript intron_variant - - - - - - rs2126326 8:14374955 A CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs10888089 8:14379929 G 137868 NM_139167.2 Transcript intron_variant - - - - - - rs10888089 8:14379929 G CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs2169421 8:14381287 C 137868 NM_139167.2 Transcript intron_variant - - - - - - rs2169421 8:14381287 C CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs1461866 8:14383631 C 137868 NM_139167.2 Transcript intron_variant - - - - - - rs1461866 8:14383631 C CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs988890 8:14386199 T 137868 NM_139167.2 Transcript intron_variant - - - - - - rs988890 8:14386199 T CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs1461852 8:14390796 T 137868 NM_139167.2 Transcript intron_variant - - - - - - rs1461852 8:14390796 T CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs11203623 8:14397266 T 137868 NM_139167.2 Transcript intron_variant - - - - - - rs11203623 8:14397266 T CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs4831305 8:14560821 A ENSESTG00000018817 ENSESTT00000047374 Transcript intron_variant - - - - - - rs4831305 8:14560821 A 137868 NM_139167.2 Transcript intron_variant - - - - - - rs4831305 8:14560821 A CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs4463427 8:14730934 G 137868 NM_139167.2 Transcript intron_variant - - - - - - rs4463427 8:14730934 G CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs10111809 8:14764767 G ENSESTG00000018809 ENSESTT00000047366 Transcript intron_variant - - - - - - rs10111809 8:14764767 G 137868 NM_139167.2 Transcript intron_variant - - - - - - rs10111809 8:14764767 G CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs9325741 8:14834767 C 137868 NM_139167.2 Transcript intron_variant - - - - - - rs9325741 8:14834767 C CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs6530827 8:14864390 G 137868 NM_139167.2 Transcript intron_variant - - - - - - rs6530827 8:14864390 G CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs7008233 8:14912335 G 137868 NM_139167.2 Transcript intron_variant - - - - - - rs7008233 8:14912335 G CCDS5992.2 CCDS5992.2 Transcript intron_variant - - - - - - rs240666 8:15654254 G - - - intergenic_variant - - - - - - rs2604315 8:15701230 G - - - intergenic_variant - - - - - - rs822267 8:16486679 T - - - intergenic_variant - - - - - - rs822966 8:16645930 G ENSESTG00000030800 ENSESTT00000077574 Transcript intron_variant - - - - - - rs2517038 8:16954840 C ENSESTG00000003663 ENSESTT00000009172 Transcript downstream_gene_variant - - - - - - DISTANCE=913 rs2517038 8:16954840 C 286097 NM_181723.2 Transcript intron_variant - - - - - - rs2517038 8:16954840 C ENSESTG00000003290 ENSESTT00000008230 Transcript intron_variant - - - - - - rs2517038 8:16954840 C CCDS5999.1 CCDS5999.1 Transcript intron_variant - - - - - - rs2517038 8:16954840 C ENSESTG00000003661 ENSESTT00000009166 Transcript intron_variant - - - - - - rs2904701 8:17100357 T 137492 NM_152415.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4044 rs2904701 8:17100357 T 29883 NM_054026.2 Transcript intron_variant - - - - - - rs2904701 8:17100357 T CCDS55202.1 CCDS55202.1 Transcript intron_variant - - - - - - rs2904701 8:17100357 T ENSESTG00000003341 ENSESTT00000008375 Transcript upstream_gene_variant - - - - - - DISTANCE=4079 rs2904701 8:17100357 T CCDS6000.2 CCDS6000.2 Transcript intron_variant - - - - - - rs2904701 8:17100357 T CCDS6001.1 CCDS6001.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4397 rs2904701 8:17100357 T CCDS47811.1 CCDS47811.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4397 rs2904701 8:17100357 T ENSESTG00000003341 ENSESTT00000008389 Transcript upstream_gene_variant - - - - - - DISTANCE=4083 rs2904701 8:17100357 T 137492 NM_001145152.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4044 rs2904701 8:17100357 T ENSESTG00000003341 ENSESTT00000008390 Transcript upstream_gene_variant - - - - - - DISTANCE=4083 rs2904701 8:17100357 T ENSESTG00000003341 ENSESTT00000008385 Transcript upstream_gene_variant - - - - - - DISTANCE=4079 rs2904701 8:17100357 T 29883 NM_013354.5 Transcript intron_variant - - - - - - rs2904701 8:17100357 T ENSESTG00000003341 ENSESTT00000008379 Transcript upstream_gene_variant - - - - - - DISTANCE=4079 rs6587036 8:17230241 C ENSESTG00000003653 ENSESTT00000009152 Transcript intron_variant - - - - - - rs6587036 8:17230241 C CCDS34851.1 CCDS34851.1 Transcript intron_variant - - - - - - rs6587036 8:17230241 C 9108 NM_004686.4 Transcript intron_variant - - - - - - rs7463636 8:17249888 T - ENSR00001439166 RegulatoryFeature regulatory_region_variant - - - - - - rs7463636 8:17249888 T ENSESTG00000003653 ENSESTT00000009152 Transcript intron_variant - - - - - - rs7463636 8:17249888 T CCDS34851.1 CCDS34851.1 Transcript intron_variant - - - - - - rs7463636 8:17249888 T 9108 NM_004686.4 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009103 Transcript downstream_gene_variant - - - - - - DISTANCE=784 rs6586626 8:17531658 C CCDS43719.1 CCDS43719.1 Transcript intron_variant - - - - - - rs6586626 8:17531658 C 57509 NM_020749.4 Transcript intron_variant - - - - - - rs6586626 8:17531658 C 57509 NM_001166393.1 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009101 Transcript intron_variant - - - - - - rs6586626 8:17531658 C 57509 NM_001001925.2 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009091 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009084 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009073 Transcript intron_variant - - - - - - rs6586626 8:17531658 C 57509 NM_001001931.2 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003411 ENSESTT00000008535 Transcript intron_variant - - - - - - rs6586626 8:17531658 C CCDS43716.1 CCDS43716.1 Transcript intron_variant - - - - - - rs6586626 8:17531658 C CCDS43718.1 CCDS43718.1 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009126 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009131 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009096 Transcript intron_variant - - - - - - rs6586626 8:17531658 C CCDS43717.1 CCDS43717.1 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009076 Transcript intron_variant - - - - - - rs6586626 8:17531658 C 57509 NM_001001924.2 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009087 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009110 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009079 Transcript intron_variant - - - - - - rs6586626 8:17531658 C CCDS55204.1 CCDS55204.1 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009123 Transcript downstream_gene_variant - - - - - - DISTANCE=688 rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009093 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003621 ENSESTT00000009119 Transcript intron_variant - - - - - - rs6586626 8:17531658 C ENSESTG00000003411 ENSESTT00000008525 Transcript intron_variant - - - - - - rs11781256 8:17640256 G ENSESTG00000003598 ENSESTT00000009008 Transcript intron_variant - - - - - - rs11781256 8:17640256 G 57509 NM_001001924.2 Transcript intron_variant - - - - - - rs11781256 8:17640256 G 57509 NM_001001925.2 Transcript intron_variant - - - - - - rs10101947 8:17717921 G CCDS6004.1 CCDS6004.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4180 rs10101947 8:17717921 G ENSESTG00000003576 ENSESTT00000008986 Transcript downstream_gene_variant - - - - - - DISTANCE=4127 rs10101947 8:17717921 G ENSESTG00000003576 ENSESTT00000008980 Transcript downstream_gene_variant - - - - - - DISTANCE=4127 rs10101947 8:17717921 G 2267 NM_201553.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3979 rs10101947 8:17717921 G ENSESTG00000003576 ENSESTT00000008984 Transcript downstream_gene_variant - - - - - - DISTANCE=4127 rs10101947 8:17717921 G 2267 NM_004467.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3979 rs10101947 8:17717921 G 2267 NM_147203.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3979 rs10101947 8:17717921 G 2267 NM_201552.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3979 rs2517324 8:17756109 C - ENSR00001439204 RegulatoryFeature regulatory_region_variant - - - - - - rs2517324 8:17756109 C ENSESTG00000003576 ENSESTT00000008984 Transcript upstream_gene_variant - - - - - - DISTANCE=3251 rs2517324 8:17756109 C 2267 NM_004467.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3062 rs2517324 8:17756109 C ENSESTG00000003576 ENSESTT00000008986 Transcript upstream_gene_variant - - - - - - DISTANCE=3258 rs2517324 8:17756109 C 2267 NM_201552.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3062 rs2517324 8:17756109 C 2267 NM_147203.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3196 rs2517324 8:17756109 C ENSESTG00000003576 ENSESTT00000008980 Transcript upstream_gene_variant - - - - - - DISTANCE=3062 rs2517324 8:17756109 C 2267 NM_201553.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3196 rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008790 Transcript intron_variant - - - - - - rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008826 Transcript intron_variant - - - - - - rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008781 Transcript intron_variant - - - - - - rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008798 Transcript intron_variant - - - - - - rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008794 Transcript intron_variant - - - - - - rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008817 Transcript intron_variant - - - - - - rs2467076 8:17799172 G 5108 NM_006197.3 Transcript intron_variant - - - - - - rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008809 Transcript intron_variant - - - - - - rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008783 Transcript intron_variant - - - - - - rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008812 Transcript intron_variant - - - - - - rs2467076 8:17799172 G CCDS47812.1 CCDS47812.1 Transcript intron_variant - - - - - - rs2467076 8:17799172 G ENSESTG00000003453 ENSESTT00000008822 Transcript intron_variant - - - - - - rs6421407 8:17921533 C 427 NM_177924.3 Transcript intron_variant - - - - - - rs6421407 8:17921533 C CCDS6005.1 CCDS6005.1 Transcript intron_variant - - - - - - rs6421407 8:17921533 C 427 NM_004315.4 Transcript intron_variant - - - - - - rs6421407 8:17921533 C ENSESTG00000024291 ENSESTT00000061456 Transcript downstream_gene_variant - - - - - - DISTANCE=3222 rs6421407 8:17921533 C CCDS6006.1 CCDS6006.1 Transcript intron_variant - - - - - - rs6421407 8:17921533 C CCDS47813.1 CCDS47813.1 Transcript intron_variant - - - - - - rs6421407 8:17921533 C ENSESTG00000003554 ENSESTT00000008901 Transcript intron_variant - - - - - - rs6421407 8:17921533 C 427 NM_001127505.1 Transcript intron_variant - - - - - - rs6421407 8:17921533 C ENSESTG00000003554 ENSESTT00000008931 Transcript intron_variant - - - - - - rs6421407 8:17921533 C ENSESTG00000024291 ENSESTT00000061480 Transcript downstream_gene_variant - - - - - - DISTANCE=3095 rs10106882 8:18077007 C 9 NM_001160175.1 Transcript intron_variant - - - - - - rs10106882 8:18077007 C CCDS6007.1 CCDS6007.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2550 rs10106882 8:18077007 C ENSESTG00000023948 ENSESTT00000060463 Transcript intron_variant - - - - - - rs10106882 8:18077007 C CCDS55205.1 CCDS55205.1 Transcript intron_variant - - - - - - rs10106882 8:18077007 C ENSESTG00000023948 ENSESTT00000060472 Transcript downstream_gene_variant - - - - - - DISTANCE=51 rs10106882 8:18077007 C 9 NM_001160179.1 Transcript intron_variant - - - - - - rs10106882 8:18077007 C ENSESTG00000023948 ENSESTT00000060437 Transcript intron_variant - - - - - - rs10106882 8:18077007 C ENSESTG00000023948 ENSESTT00000060454 Transcript intron_variant - - - - - - rs10106882 8:18077007 C 9 NM_001160170.1 Transcript intron_variant - - - - - - rs10106882 8:18077007 C 9 NM_001160173.1 Transcript intron_variant - - - - - - rs10106882 8:18077007 C 9 NM_000662.5 Transcript intron_variant - - - - - - rs10106882 8:18077007 C 9 NM_001160172.1 Transcript intron_variant - - - - - - rs10106882 8:18077007 C 9 NM_001160171.1 Transcript intron_variant - - - - - - rs10106882 8:18077007 C 9 NM_001160176.1 Transcript intron_variant - - - - - - rs10106882 8:18077007 C 9 NM_001160174.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2170 rs6982949 8:18080923 A 9 NM_001160175.1 Transcript 3_prime_UTR_variant 1792 - - - - - rs6982949 8:18080923 A CCDS6007.1 CCDS6007.1 Transcript downstream_gene_variant - - - - - - DISTANCE=494 rs6982949 8:18080923 A ENSESTG00000023948 ENSESTT00000060463 Transcript downstream_gene_variant - - - - - - DISTANCE=1147 rs6982949 8:18080923 A CCDS55205.1 CCDS55205.1 Transcript downstream_gene_variant - - - - - - DISTANCE=494 rs6982949 8:18080923 A ENSESTG00000023948 ENSESTT00000060472 Transcript downstream_gene_variant - - - - - - DISTANCE=3967 rs6982949 8:18080923 A 9 NM_001160179.1 Transcript 3_prime_UTR_variant 1734 - - - - - rs6982949 8:18080923 A ENSESTG00000023948 ENSESTT00000060437 Transcript downstream_gene_variant - - - - - - DISTANCE=902 rs6982949 8:18080923 A ENSESTG00000023948 ENSESTT00000060454 Transcript downstream_gene_variant - - - - - - DISTANCE=1316 rs6982949 8:18080923 A 9 NM_001160170.1 Transcript 3_prime_UTR_variant 2058 - - - - - rs6982949 8:18080923 A 9 NM_001160173.1 Transcript 3_prime_UTR_variant 1674 - - - - - rs6982949 8:18080923 A 9 NM_000662.5 Transcript 3_prime_UTR_variant 1524 - - - - - rs6982949 8:18080923 A 9 NM_001160172.1 Transcript 3_prime_UTR_variant 1829 - - - - - rs6982949 8:18080923 A 9 NM_001160171.1 Transcript 3_prime_UTR_variant 1908 - - - - - rs6982949 8:18080923 A 9 NM_001160176.1 Transcript 3_prime_UTR_variant 1642 - - - - - rs6982949 8:18080923 A 9 NM_001160174.1 Transcript 3_prime_UTR_variant 1747 - - - - - rs1603297 8:18213685 G - - - intergenic_variant - - - - - - rs1603299 8:18222534 C - - - intergenic_variant - - - - - - rs1845737 8:18223167 C - - - intergenic_variant - - - - - - rs7010673 8:18287126 A - - - intergenic_variant - - - - - - rs2410560 8:18296191 C - - - intergenic_variant - - - - - - rs1495752 8:18303262 G - - - intergenic_variant - - - - - - rs11203967 8:18401619 G 23362 NM_015310.3 Transcript intron_variant - - - - - - rs11203967 8:18401619 G ENSESTG00000024025 ENSESTT00000060955 Transcript intron_variant - - - - - - rs11203967 8:18401619 G CCDS43720.1 CCDS43720.1 Transcript intron_variant - - - - - - rs11203967 8:18401619 G CCDS34854.1 CCDS34854.1 Transcript intron_variant - - - - - - rs11203967 8:18401619 G 23362 NM_206909.2 Transcript intron_variant - - - - - - rs11203967 8:18401619 G ENSESTG00000024157 ENSESTT00000061031 Transcript intron_variant - - - - - - rs334212 8:18910643 G ENSESTG00000024003 ENSESTT00000060558 Transcript intron_variant - - - - - - rs12681061 8:18932525 G ENSESTG00000024003 ENSESTT00000060558 Transcript intron_variant - - - - - - rs7461995 8:18954048 C - ENSR00001386994 RegulatoryFeature regulatory_region_variant - - - - - - rs7461995 8:18954048 C ENSESTG00000013390 ENSESTT00000033540 Transcript intron_variant - - - - - - rs597602 8:19042504 C 100128993 NR_038919.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7819880 8:19178096 C 63898 NM_001174159.1 Transcript intron_variant - - - - - - rs7819880 8:19178096 C CCDS6009.1 CCDS6009.1 Transcript intron_variant - - - - - - rs7819880 8:19178096 C ENSESTG00000013408 ENSESTT00000033602 Transcript intron_variant - - - - - - rs7819880 8:19178096 C ENSESTG00000013408 ENSESTT00000033592 Transcript intron_variant - - - - - - rs7819880 8:19178096 C 63898 NM_001174160.1 Transcript intron_variant - - - - - - rs7819880 8:19178096 C 63898 NM_022071.3 Transcript intron_variant - - - - - - rs7819880 8:19178096 C ENSESTG00000013408 ENSESTT00000033588 Transcript intron_variant - - - - - - rs7819880 8:19178096 C CCDS55206.1 CCDS55206.1 Transcript intron_variant - - - - - - rs10086448 8:19333743 G 55790 NR_024040.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10086448 8:19333743 G 55790 NM_001130518.1 Transcript intron_variant - - - - - - rs10086448 8:19333743 G CCDS6010.1 CCDS6010.1 Transcript intron_variant - - - - - - rs10086448 8:19333743 G ENSESTG00000013484 ENSESTT00000033761 Transcript intron_variant - - - - - - rs10086448 8:19333743 G 55790 NM_018371.4 Transcript intron_variant - - - - - - rs2958596 8:19389362 G 55790 NR_024040.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2958596 8:19389362 G ENSESTG00000013470 ENSESTT00000033734 Transcript intron_variant - - - - - - rs2958596 8:19389362 G 55790 NM_001130518.1 Transcript intron_variant - - - - - - rs2958596 8:19389362 G ENSESTG00000013470 ENSESTT00000033748 Transcript intron_variant - - - - - - rs2958596 8:19389362 G ENSESTG00000013470 ENSESTT00000033742 Transcript intron_variant - - - - - - rs2958596 8:19389362 G ENSESTG00000013470 ENSESTT00000033730 Transcript intron_variant - - - - - - rs2958596 8:19389362 G 55790 NM_018371.4 Transcript intron_variant - - - - - - rs10108078 8:19532731 G 55790 NR_024040.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10108078 8:19532731 G ENSESTG00000013470 ENSESTT00000033734 Transcript intron_variant - - - - - - rs10108078 8:19532731 G ENSESTG00000013470 ENSESTT00000033730 Transcript intron_variant - - - - - - rs10108078 8:19532731 G 55790 NM_018371.4 Transcript intron_variant - - - - - - rs11786265 8:19851658 A - - - intergenic_variant - - - - - - rs6990271 8:19944153 C - ENSR00001387190 RegulatoryFeature regulatory_region_variant - - - - - - rs6990271 8:19944153 C - - - intergenic_variant - - - - - - rs4637849 8:19950741 T - - - intergenic_variant - - - - - - rs11204093 8:19987746 G - - - intergenic_variant - - - - - - rs4921695 8:20039902 T ENSESTG00000011521 ENSESTT00000028902 Transcript intron_variant - - - - - - rs4921695 8:20039902 T CCDS47815.1 CCDS47815.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1427 rs4921695 8:20039902 T 6570 NM_001142324.1 Transcript intron_variant - - - - - - rs4921695 8:20039902 T CCDS6013.1 CCDS6013.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1427 rs4921695 8:20039902 T 6570 NM_003053.3 Transcript intron_variant - - - - - - rs4921695 8:20039902 T CCDS47814.1 CCDS47814.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1427 rs4921695 8:20039902 T 6570 NM_001135691.2 Transcript intron_variant - - - - - - rs4921695 8:20039902 T 6570 NM_001142325.1 Transcript intron_variant - - - - - - rs904003 8:20107143 G 11178 NM_021020.2 Transcript 3_prime_UTR_variant 1992 - - - - - rs904003 8:20107143 G CCDS6015.1 CCDS6015.1 Transcript downstream_gene_variant - - - - - - DISTANCE=90 rs904003 8:20107143 G ENSESTG00000011518 ENSESTT00000028879 Transcript downstream_gene_variant - - - - - - DISTANCE=3838 rs10788701 8:20241190 G - - - intergenic_variant - - - - - - rs4258019 8:20308325 C - - - intergenic_variant - - - - - - rs6586918 8:20403171 C - - - intergenic_variant - - - - - - rs6586935 8:20745970 C - - - intergenic_variant - - - - - - rs2044064 8:20746174 A - - - intergenic_variant - - - - - - rs579774 8:20802019 G - - - intergenic_variant - - - - - - rs519211 8:20831049 G 286114 NR_033894.1 Transcript upstream_gene_variant - - - - - - DISTANCE=448 rs519211 8:20831049 G ENSESTG00000011511 ENSESTT00000028872 Transcript intron_variant - - - - - - rs504472 8:20834058 G 286114 NR_033894.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs504472 8:20834058 G ENSESTG00000011511 ENSESTT00000028872 Transcript upstream_gene_variant - - - - - - DISTANCE=2637 rs1480996 8:21464896 C - - - intergenic_variant - - - - - - rs2410693 8:21465837 C - - - intergenic_variant - - - - - - rs148268306 8:21620470 T CCDS55207.1 CCDS55207.1 Transcript intron_variant - - - - - - rs148268306 8:21620470 T CCDS47816.1 CCDS47816.1 Transcript intron_variant - - - - - - rs148268306 8:21620470 T 2675 NM_001165038.1 Transcript intron_variant - - - - - - rs148268306 8:21620470 T ENSESTG00000034596 ENSESTT00000087541 Transcript intron_variant - - - - - - rs148268306 8:21620470 T 2675 NM_001495.4 Transcript intron_variant - - - - - - rs148268306 8:21620470 T CCDS55208.1 CCDS55208.1 Transcript intron_variant - - - - - - rs148268306 8:21620470 T 2675 NM_001165039.1 Transcript intron_variant - - - - - - rs900777 8:21817568 A - ENSR00001387397 RegulatoryFeature regulatory_region_variant - - - - - - rs900777 8:21817568 A ENSESTG00000034496 ENSESTT00000087391 Transcript intron_variant - - - - - - rs900777 8:21817568 A ENSESTG00000034496 ENSESTT00000087362 Transcript intron_variant - - - - - - rs900777 8:21817568 A 23039 NM_015024.4 Transcript intron_variant - - - - - - rs900777 8:21817568 A CCDS47818.1 CCDS47818.1 Transcript intron_variant - - - - - - rs900777 8:21817568 A ENSESTG00000034496 ENSESTT00000087400 Transcript intron_variant - - - - - - rs900777 8:21817568 A ENSESTG00000034496 ENSESTT00000087252 Transcript intron_variant - - - - - - rs900777 8:21817568 A ENSESTG00000034496 ENSESTT00000087375 Transcript intron_variant - - - - - - rs900777 8:21817568 A ENSESTG00000034496 ENSESTT00000087394 Transcript intron_variant - - - - - - rs4307344 8:22401907 A 5533 NM_005605.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3250 rs4307344 8:22401907 A ENSESTG00000008103 ENSESTT00000020540 Transcript downstream_gene_variant - - - - - - DISTANCE=3252 rs4307344 8:22401907 A ENSESTG00000008103 ENSESTT00000020581 Transcript downstream_gene_variant - - - - - - DISTANCE=3252 rs4307344 8:22401907 A ENSESTG00000008103 ENSESTT00000020572 Transcript downstream_gene_variant - - - - - - DISTANCE=3252 rs4307344 8:22401907 A CCDS34859.1 CCDS34859.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3592 rs4307344 8:22401907 A ENSESTG00000008103 ENSESTT00000020562 Transcript downstream_gene_variant - - - - - - DISTANCE=3408 rs4307344 8:22401907 A ENSESTG00000008160 ENSESTT00000020604 Transcript upstream_gene_variant - - - - - - DISTANCE=602 rs4307344 8:22401907 A ENSESTG00000008720 ENSESTT00000021886 Transcript intron_variant - - - - - - rs4307344 8:22401907 A ENSESTG00000008103 ENSESTT00000020568 Transcript downstream_gene_variant - - - - - - DISTANCE=4550 rs4307344 8:22401907 A CCDS59093.1 CCDS59093.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3592 rs4307344 8:22401907 A ENSESTG00000008103 ENSESTT00000020548 Transcript downstream_gene_variant - - - - - - DISTANCE=3408 rs4307344 8:22401907 A ENSESTG00000008160 ENSESTT00000020602 Transcript upstream_gene_variant - - - - - - DISTANCE=595 rs4307344 8:22401907 A ENSESTG00000008103 ENSESTT00000020561 Transcript downstream_gene_variant - - - - - - DISTANCE=3252 rs4307344 8:22401907 A ENSESTG00000008160 ENSESTT00000020611 Transcript upstream_gene_variant - - - - - - DISTANCE=3410 rs4307344 8:22401907 A ENSESTG00000008720 ENSESTT00000021883 Transcript intron_variant - - - - - - rs4307344 8:22401907 A ENSESTG00000008103 ENSESTT00000020591 Transcript downstream_gene_variant - - - - - - DISTANCE=3272 rs4307344 8:22401907 A 5533 NM_001243974.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3250 rs4307344 8:22401907 A CCDS59094.1 CCDS59094.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3592 rs4307344 8:22401907 A 5533 NM_001243975.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3250 rs4307344 8:22401907 A ENSESTG00000008103 ENSESTT00000020553 Transcript downstream_gene_variant - - - - - - DISTANCE=4550 rs4872514 8:22441477 G - ENSR00001387599 RegulatoryFeature regulatory_region_variant - - - - - - rs4872514 8:22441477 G ENSESTG00000008261 ENSESTT00000020869 Transcript intron_variant - - - - - - rs4872514 8:22441477 G CCDS34860.1 CCDS34860.1 Transcript intron_variant - - - - - - rs4872514 8:22441477 G ENSESTG00000008261 ENSESTT00000020883 Transcript intron_variant - - - - - - rs4872514 8:22441477 G CCDS6032.2 CCDS6032.2 Transcript intron_variant - - - - - - rs4872514 8:22441477 G ENSESTG00000008261 ENSESTT00000020904 Transcript intron_variant - - - - - - rs4872514 8:22441477 G ENSESTG00000008261 ENSESTT00000020901 Transcript intron_variant - - - - - - rs4872514 8:22441477 G ENSESTG00000008261 ENSESTT00000020887 Transcript intron_variant - - - - - - rs4872514 8:22441477 G CCDS34861.1 CCDS34861.1 Transcript intron_variant - - - - - - rs4872514 8:22441477 G ENSESTG00000008261 ENSESTT00000020897 Transcript intron_variant - - - - - - rs4872514 8:22441477 G ENSESTG00000008261 ENSESTT00000020872 Transcript intron_variant - - - - - - rs4872514 8:22441477 G ENSESTG00000008261 ENSESTT00000020896 Transcript intron_variant - - - - - - rs4872514 8:22441477 G 64236 NM_176871.3 Transcript intron_variant - - - - - - rs4872514 8:22441477 G 64236 NM_021630.5 Transcript intron_variant - - - - - - rs4872514 8:22441477 G 64236 NM_198042.3 Transcript intron_variant - - - - - - rs4872514 8:22441477 G ENSESTG00000008261 ENSESTT00000020880 Transcript downstream_gene_variant - - - - - - DISTANCE=3331 rs4451313 8:22516853 C - ENSR00001439526 RegulatoryFeature regulatory_region_variant - - - - - - rs4451313 8:22516853 C ENSESTG00000008638 ENSESTT00000021719 Transcript intron_variant - - - - - - rs4451313 8:22516853 C CCDS47825.1 CCDS47825.1 Transcript intron_variant - - - - - - rs4451313 8:22516853 C ENSESTG00000008638 ENSESTT00000021786 Transcript intron_variant - - - - - - rs4451313 8:22516853 C ENSESTG00000008638 ENSESTT00000021780 Transcript intron_variant - - - - - - rs4451313 8:22516853 C 55909 NM_018688.4 Transcript intron_variant - - - - - - rs6557605 8:22803229 C - - - intergenic_variant - - - - - - rs12675756 8:22934523 T 286059 NR_038873.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs310314 8:23704157 C CCDS6043.1 CCDS6043.1 Transcript intron_variant - - - - - - rs310314 8:23704157 C 6781 NM_003155.2 Transcript intron_variant - - - - - - rs4345567 8:23766089 G - - - intergenic_variant - - - - - - rs1602652 8:24302244 G CCDS6045.1 CCDS6045.1 Transcript intron_variant - - - - - - rs1602652 8:24302244 G ENSESTG00000018889 ENSESTT00000047631 Transcript intron_variant - - - - - - rs1602652 8:24302244 G 8756 NM_003817.3 Transcript intron_variant - - - - - - rs1873709 8:24323702 A CCDS6045.1 CCDS6045.1 Transcript intron_variant - - - - - - rs1873709 8:24323702 A ENSESTG00000018889 ENSESTT00000047631 Transcript intron_variant - - - - - - rs1873709 8:24323702 A 8756 NM_003817.3 Transcript intron_variant - - - - - - rs2712774 8:24612697 A - - - intergenic_variant - - - - - - rs196867 8:24770904 G - ENSR00001388046 RegulatoryFeature regulatory_region_variant - - - - - - rs196867 8:24770904 G 4741 NM_005382.2 Transcript upstream_gene_variant - - - - - - DISTANCE=370 rs196867 8:24770904 G CCDS47831.1 CCDS47831.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2262 rs196867 8:24770904 G ENSESTG00000018985 ENSESTT00000047826 Transcript upstream_gene_variant - - - - - - DISTANCE=1551 rs196867 8:24770904 G 4741 NM_001105541.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1551 rs196867 8:24770904 G CCDS6046.1 CCDS6046.1 Transcript upstream_gene_variant - - - - - - DISTANCE=403 rs6992621 8:24825860 A - - - intergenic_variant - - - - - - rs6557796 8:24874602 T - - - intergenic_variant - - - - - - rs11995076 8:25053009 A - ENSR00001388096 RegulatoryFeature regulatory_region_variant - - - - - - rs11995076 8:25053009 A 80005 NM_024940.6 Transcript intron_variant - - - - - - rs11995076 8:25053009 A ENSESTG00000029411 ENSESTT00000074064 Transcript intron_variant - - - - - - rs11995076 8:25053009 A CCDS6047.1 CCDS6047.1 Transcript intron_variant - - - - - - rs4872296 8:25058050 C 80005 NM_024940.6 Transcript intron_variant - - - - - - rs4872296 8:25058050 C ENSESTG00000029411 ENSESTT00000074064 Transcript intron_variant - - - - - - rs4872296 8:25058050 C CCDS6047.1 CCDS6047.1 Transcript intron_variant - - - - - - rs10095623 8:25065816 C 80005 NM_024940.6 Transcript intron_variant - - - - - - rs10095623 8:25065816 C ENSESTG00000029411 ENSESTT00000074064 Transcript intron_variant - - - - - - rs10095623 8:25065816 C CCDS6047.1 CCDS6047.1 Transcript intron_variant - - - - - - rs7832979 8:25070826 C 80005 NM_024940.6 Transcript intron_variant - - - - - - rs7832979 8:25070826 C ENSESTG00000029411 ENSESTT00000074064 Transcript intron_variant - - - - - - rs7832979 8:25070826 C CCDS6047.1 CCDS6047.1 Transcript intron_variant - - - - - - rs1473020 8:25102985 T 80005 NM_024940.6 Transcript intron_variant - - - - - - rs1473020 8:25102985 T ENSESTG00000029411 ENSESTT00000074064 Transcript intron_variant - - - - - - rs1473020 8:25102985 T CCDS6047.1 CCDS6047.1 Transcript intron_variant - - - - - - rs2468892 8:25147287 G 80005 NM_024940.6 Transcript intron_variant - - - - - - rs2468892 8:25147287 G ENSESTG00000029411 ENSESTT00000074099 Transcript intron_variant - - - - - - rs2468892 8:25147287 G ENSESTG00000029411 ENSESTT00000074064 Transcript intron_variant - - - - - - rs2468892 8:25147287 G CCDS6047.1 CCDS6047.1 Transcript intron_variant - - - - - - rs10110351 8:25200148 G ENSESTG00000029519 ENSESTT00000074362 Transcript intron_variant - - - - - - rs10110351 8:25200148 G ENSESTG00000029489 ENSESTT00000074247 Transcript downstream_gene_variant - - - - - - DISTANCE=1677 rs10110351 8:25200148 G 80005 NM_024940.6 Transcript intron_variant - - - - - - rs10110351 8:25200148 G CCDS6047.1 CCDS6047.1 Transcript intron_variant - - - - - - rs6982656 8:25233659 G ENSESTG00000029519 ENSESTT00000074362 Transcript intron_variant - - - - - - rs6982656 8:25233659 G ENSESTG00000029519 ENSESTT00000074388 Transcript intron_variant - - - - - - rs6982656 8:25233659 G ENSESTG00000029519 ENSESTT00000074378 Transcript intron_variant - - - - - - rs6982656 8:25233659 G 80005 NM_024940.6 Transcript intron_variant - - - - - - rs6982656 8:25233659 G CCDS6047.1 CCDS6047.1 Transcript intron_variant - - - - - - rs2979743 8:25397884 A - - - intergenic_variant - - - - - - rs4262332 8:25426172 T - - - intergenic_variant - - - - - - rs2467702 8:25546336 T ENSESTG00000029730 ENSESTT00000074806 Transcript downstream_gene_variant - - - - - - DISTANCE=1658 rs4871961 8:25792296 G ENSESTG00000029752 ENSESTT00000074882 Transcript intron_variant - - - - - - rs4871961 8:25792296 G CCDS43726.1 CCDS43726.1 Transcript intron_variant - - - - - - rs4871961 8:25792296 G ENSESTG00000029752 ENSESTT00000074846 Transcript intron_variant - - - - - - rs4871961 8:25792296 G 64641 NM_022659.3 Transcript intron_variant - - - - - - rs6557871 8:25807114 A ENSESTG00000029752 ENSESTT00000074882 Transcript intron_variant - - - - - - rs6557871 8:25807114 A CCDS43726.1 CCDS43726.1 Transcript intron_variant - - - - - - rs6557871 8:25807114 A ENSESTG00000029752 ENSESTT00000074846 Transcript intron_variant - - - - - - rs6557871 8:25807114 A 64641 NM_022659.3 Transcript intron_variant - - - - - - rs6557874 8:25885386 T ENSESTG00000029752 ENSESTT00000074882 Transcript intron_variant - - - - - - rs6557874 8:25885386 T CCDS43726.1 CCDS43726.1 Transcript intron_variant - - - - - - rs6557874 8:25885386 T ENSESTG00000029752 ENSESTT00000074846 Transcript intron_variant - - - - - - rs6557874 8:25885386 T 64641 NM_022659.3 Transcript intron_variant - - - - - - rs2584189 8:26430075 G - ENSR00001388324 RegulatoryFeature regulatory_region_variant - - - - - - rs2584189 8:26430075 G 1808 NM_001197293.2 Transcript intron_variant - - - - - - rs2584189 8:26430075 G ENSESTG00000029960 ENSESTT00000075631 Transcript upstream_gene_variant - - - - - - DISTANCE=4503 rs2584189 8:26430075 G ENSESTG00000029960 ENSESTT00000075618 Transcript upstream_gene_variant - - - - - - DISTANCE=4503 rs10866857 8:27054030 T ENSESTG00000021346 ENSESTT00000053567 Transcript intron_variant - - - - - - rs6557997 8:27244214 T ENSESTG00000021456 ENSESTT00000054390 Transcript intron_variant - - - - - - rs6557997 8:27244214 T 2185 NM_173174.2 Transcript intron_variant - - - - - - rs6557997 8:27244214 T 2185 NM_004103.4 Transcript intron_variant - - - - - - rs6557997 8:27244214 T ENSESTG00000021456 ENSESTT00000054432 Transcript intron_variant - - - - - - rs6557997 8:27244214 T ENSESTG00000021456 ENSESTT00000054419 Transcript intron_variant - - - - - - rs6557997 8:27244214 T ENSESTG00000021456 ENSESTT00000054369 Transcript intron_variant - - - - - - rs6557997 8:27244214 T 2185 NM_173175.2 Transcript intron_variant - - - - - - rs6557997 8:27244214 T ENSESTG00000021456 ENSESTT00000054460 Transcript intron_variant - - - - - - rs6557997 8:27244214 T ENSESTG00000021456 ENSESTT00000054408 Transcript intron_variant - - - - - - rs6557997 8:27244214 T ENSESTG00000021456 ENSESTT00000054446 Transcript intron_variant - - - - - - rs6557997 8:27244214 T 2185 NM_173176.2 Transcript intron_variant - - - - - - rs4333544 8:27249633 G ENSESTG00000021456 ENSESTT00000054390 Transcript intron_variant - - - - - - rs4333544 8:27249633 G 2185 NM_173174.2 Transcript intron_variant - - - - - - rs4333544 8:27249633 G 2185 NM_004103.4 Transcript intron_variant - - - - - - rs4333544 8:27249633 G ENSESTG00000021456 ENSESTT00000054432 Transcript intron_variant - - - - - - rs4333544 8:27249633 G ENSESTG00000021456 ENSESTT00000054419 Transcript intron_variant - - - - - - rs4333544 8:27249633 G ENSESTG00000021456 ENSESTT00000054369 Transcript intron_variant - - - - - - rs4333544 8:27249633 G 2185 NM_173175.2 Transcript intron_variant - - - - - - rs4333544 8:27249633 G ENSESTG00000021456 ENSESTT00000054460 Transcript intron_variant - - - - - - rs4333544 8:27249633 G ENSESTG00000021456 ENSESTT00000054408 Transcript intron_variant - - - - - - rs4333544 8:27249633 G ENSESTG00000021456 ENSESTT00000054446 Transcript intron_variant - - - - - - rs4333544 8:27249633 G 2185 NM_173176.2 Transcript intron_variant - - - - - - rs2741345 8:27256427 G ENSESTG00000021456 ENSESTT00000054390 Transcript intron_variant - - - - - - rs2741345 8:27256427 G 2185 NM_173174.2 Transcript intron_variant - - - - - - rs2741345 8:27256427 G 2185 NM_004103.4 Transcript intron_variant - - - - - - rs2741345 8:27256427 G ENSESTG00000021456 ENSESTT00000054432 Transcript intron_variant - - - - - - rs2741345 8:27256427 G ENSESTG00000021456 ENSESTT00000054419 Transcript intron_variant - - - - - - rs2741345 8:27256427 G ENSESTG00000021456 ENSESTT00000054369 Transcript intron_variant - - - - - - rs2741345 8:27256427 G CCDS6058.1 CCDS6058.1 Transcript intron_variant - - - - - - rs2741345 8:27256427 G 2185 NM_173175.2 Transcript intron_variant - - - - - - rs2741345 8:27256427 G CCDS6057.1 CCDS6057.1 Transcript intron_variant - - - - - - rs2741345 8:27256427 G ENSESTG00000021456 ENSESTT00000054460 Transcript downstream_gene_variant - - - - - - DISTANCE=2616 rs2741345 8:27256427 G ENSESTG00000021456 ENSESTT00000054408 Transcript intron_variant - - - - - - rs2741345 8:27256427 G ENSESTG00000021456 ENSESTT00000054446 Transcript intron_variant - - - - - - rs2741345 8:27256427 G 2185 NM_173176.2 Transcript intron_variant - - - - - - rs2685319 8:27780789 A ENSESTG00000021973 ENSESTT00000055308 Transcript upstream_gene_variant - - - - - - DISTANCE=1503 rs2685319 8:27780789 A 286133 NM_173833.5 Transcript intron_variant - - - - - - rs2685319 8:27780789 A CCDS6064.1 CCDS6064.1 Transcript intron_variant - - - - - - rs904052 8:28208396 G 55893 NM_018660.2 Transcript intron_variant - - - - - - rs904052 8:28208396 G CCDS6067.1 CCDS6067.1 Transcript intron_variant - - - - - - rs352225 8:28411264 G 7976 NM_145866.1 Transcript intron_variant - - - - - - rs352225 8:28411264 G CCDS6069.1 CCDS6069.1 Transcript intron_variant - - - - - - rs352225 8:28411264 G 7976 NM_017412.3 Transcript intron_variant - - - - - - rs352225 8:28411264 G ENSESTG00000023930 ENSESTT00000060419 Transcript intron_variant - - - - - - rs352225 8:28411264 G ENSESTG00000023930 ENSESTT00000060412 Transcript intron_variant - - - - - - rs6996641 8:28507368 T - - - intergenic_variant - - - - - - rs7462400 8:28633124 C ENSESTG00000024018 ENSESTT00000060627 Transcript intron_variant - - - - - - rs7462400 8:28633124 C ENSESTG00000024080 ENSESTT00000061083 Transcript intron_variant - - - - - - rs7462400 8:28633124 C 55756 NM_018250.3 Transcript intron_variant - - - - - - rs7462400 8:28633124 C ENSESTG00000024080 ENSESTT00000061054 Transcript intron_variant - - - - - - rs7462400 8:28633124 C 55756 NM_001145159.2 Transcript intron_variant - - - - - - rs7462400 8:28633124 C CCDS55216.1 CCDS55216.1 Transcript intron_variant - - - - - - rs7462400 8:28633124 C 55756 NR_026826.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs7462400 8:28633124 C ENSESTG00000024080 ENSESTT00000061099 Transcript intron_variant - - - - - - rs7462400 8:28633124 C 55756 NM_001172562.1 Transcript intron_variant - - - - - - rs7462400 8:28633124 C CCDS55215.1 CCDS55215.1 Transcript intron_variant - - - - - - rs7462400 8:28633124 C CCDS34873.1 CCDS34873.1 Transcript intron_variant - - - - - - rs171311 8:28663083 C ENSESTG00000024080 ENSESTT00000061083 Transcript intron_variant - - - - - - rs171311 8:28663083 C 55756 NM_018250.3 Transcript intron_variant - - - - - - rs171311 8:28663083 C ENSESTG00000024080 ENSESTT00000061054 Transcript intron_variant - - - - - - rs171311 8:28663083 C 55756 NM_001145159.2 Transcript intron_variant - - - - - - rs171311 8:28663083 C CCDS55216.1 CCDS55216.1 Transcript intron_variant - - - - - - rs171311 8:28663083 C 55756 NR_026826.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs171311 8:28663083 C ENSESTG00000024080 ENSESTT00000061099 Transcript intron_variant - - - - - - rs171311 8:28663083 C 55756 NM_001172562.1 Transcript intron_variant - - - - - - rs171311 8:28663083 C CCDS55215.1 CCDS55215.1 Transcript intron_variant - - - - - - rs171311 8:28663083 C CCDS34873.1 CCDS34873.1 Transcript intron_variant - - - - - - rs4732660 8:28818103 C 79618 NM_024567.3 Transcript intron_variant - - - - - - rs4732660 8:28818103 C 79618 NM_001135726.1 Transcript intron_variant - - - - - - rs4732660 8:28818103 C ENSESTG00000024030 ENSESTT00000060824 Transcript intron_variant - - - - - - rs4732660 8:28818103 C CCDS6071.1 CCDS6071.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3282 rs13263175 8:28835045 C 79618 NM_024567.3 Transcript intron_variant - - - - - - rs13263175 8:28835045 C 79618 NM_001135726.1 Transcript intron_variant - - - - - - rs13263175 8:28835045 C ENSESTG00000024030 ENSESTT00000060824 Transcript intron_variant - - - - - - rs13263175 8:28835045 C CCDS6071.1 CCDS6071.1 Transcript intron_variant - - - - - - rs6558088 8:28886975 C - ENSR00001388799 RegulatoryFeature regulatory_region_variant - - - - - - rs6558088 8:28886975 C 79618 NM_024567.3 Transcript intron_variant - - - - - - rs6558088 8:28886975 C ENSESTG00000034215 ENSESTT00000086519 Transcript intron_variant - - - - - - rs6558088 8:28886975 C ENSESTG00000034215 ENSESTT00000086502 Transcript intron_variant - - - - - - rs6558088 8:28886975 C ENSESTG00000034215 ENSESTT00000086503 Transcript intron_variant - - - - - - rs6558088 8:28886975 C ENSESTG00000024030 ENSESTT00000060824 Transcript intron_variant - - - - - - rs6558088 8:28886975 C 79618 NM_001135726.1 Transcript intron_variant - - - - - - rs6558088 8:28886975 C ENSESTG00000034215 ENSESTT00000086506 Transcript intron_variant - - - - - - rs6558088 8:28886975 C CCDS6071.1 CCDS6071.1 Transcript intron_variant - - - - - - rs2943064 8:29128224 C - - - intergenic_variant - - - - - - rs686480 8:29258298 G - - - intergenic_variant - - - - - - rs4732692 8:29435207 T - - - intergenic_variant - - - - - - rs10103158 8:29437895 C - - - intergenic_variant - - - - - - rs9286363 8:29673372 G - ENSR00001389028 RegulatoryFeature regulatory_region_variant - - - - - - rs9286363 8:29673372 G - - - intergenic_variant - - - - - - rs7842730 8:29912892 C - - - intergenic_variant - - - - - - rs2551711 8:30556033 C - ENSR00001440139 RegulatoryFeature regulatory_region_variant - - - - - - rs2551711 8:30556033 C ENSESTG00000009880 ENSESTT00000024771 Transcript intron_variant - - - - - - rs2551711 8:30556033 C ENSESTG00000009880 ENSESTT00000024763 Transcript intron_variant - - - - - - rs2551711 8:30556033 C ENSESTG00000009880 ENSESTT00000024778 Transcript intron_variant - - - - - - rs2551711 8:30556033 C ENSESTG00000009880 ENSESTT00000024767 Transcript intron_variant - - - - - - rs2551711 8:30556033 C 2936 NM_001195103.1 Transcript intron_variant - - - - - - rs2551711 8:30556033 C ENSESTG00000009880 ENSESTT00000024781 Transcript intron_variant - - - - - - rs2551711 8:30556033 C CCDS34877.1 CCDS34877.1 Transcript intron_variant - - - - - - rs2551711 8:30556033 C 2936 NM_001195102.1 Transcript intron_variant - - - - - - rs2551711 8:30556033 C 2936 NM_000637.3 Transcript intron_variant - - - - - - rs2551711 8:30556033 C ENSESTG00000009880 ENSESTT00000024773 Transcript intron_variant - - - - - - rs2551711 8:30556033 C CCDS56530.1 CCDS56530.1 Transcript intron_variant - - - - - - rs2551711 8:30556033 C 2936 NM_001195104.1 Transcript intron_variant - - - - - - rs2551711 8:30556033 C CCDS56531.1 CCDS56531.1 Transcript intron_variant - - - - - - rs2551711 8:30556033 C CCDS56532.1 CCDS56532.1 Transcript intron_variant - - - - - - rs9772303 8:30615427 A ENSESTG00000009820 ENSESTT00000024577 Transcript intron_variant - - - - - - rs9772303 8:30615427 A 7993 NM_005671.2 Transcript intron_variant - - - - - - rs9772303 8:30615427 A ENSESTG00000009820 ENSESTT00000024583 Transcript intron_variant - - - - - - rs9772303 8:30615427 A ENSESTG00000009820 ENSESTT00000024575 Transcript intron_variant - - - - - - rs13249031 8:30622888 T ENSESTG00000009820 ENSESTT00000024577 Transcript downstream_gene_variant - - - - - - DISTANCE=2049 rs13249031 8:30622888 T 7993 NM_005671.2 Transcript intron_variant - - - - - - rs13249031 8:30622888 T ENSESTG00000009820 ENSESTT00000024583 Transcript downstream_gene_variant - - - - - - DISTANCE=2076 rs13249031 8:30622888 T ENSESTG00000009820 ENSESTT00000024575 Transcript downstream_gene_variant - - - - - - DISTANCE=2049 rs2737328 8:30960127 G CCDS6082.1 CCDS6082.1 Transcript intron_variant - - - - - - rs2737328 8:30960127 G ENSESTG00000010999 ENSESTT00000027573 Transcript intron_variant - - - - - - rs2737328 8:30960127 G ENSESTG00000011057 ENSESTT00000027707 Transcript intron_variant - - - - - - rs2737328 8:30960127 G ENSESTG00000010999 ENSESTT00000027558 Transcript downstream_gene_variant - - - - - - DISTANCE=1740 rs2737328 8:30960127 G 7486 NM_000553.4 Transcript intron_variant - - - - - - rs6983554 8:31192241 G - - - intergenic_variant - - - - - - rs13253650 8:31192289 G - - - intergenic_variant - - - - - - rs11781288 8:31192314 G - - - intergenic_variant - - - - - - rs7812320 8:31400397 C - - - intergenic_variant - - - - - - rs405392 8:31806169 A 3084 NM_001159999.1 Transcript intron_variant - - - - - - rs405392 8:31806169 A CCDS55218.1 CCDS55218.1 Transcript intron_variant - - - - - - rs405392 8:31806169 A 3084 NM_001160001.1 Transcript intron_variant - - - - - - rs405392 8:31806169 A 3084 NM_013962.2 Transcript intron_variant - - - - - - rs405392 8:31806169 A CCDS47836.1 CCDS47836.1 Transcript intron_variant - - - - - - rs405392 8:31806169 A 3084 NM_001159995.1 Transcript intron_variant - - - - - - rs4733287 8:31885716 T 3084 NM_001159999.1 Transcript intron_variant - - - - - - rs4733287 8:31885716 T CCDS55218.1 CCDS55218.1 Transcript intron_variant - - - - - - rs4733287 8:31885716 T 3084 NM_001160001.1 Transcript intron_variant - - - - - - rs4733287 8:31885716 T 3084 NM_013962.2 Transcript intron_variant - - - - - - rs4733287 8:31885716 T CCDS47836.1 CCDS47836.1 Transcript intron_variant - - - - - - rs4733287 8:31885716 T 3084 NM_001159995.1 Transcript intron_variant - - - - - - rs1947733 8:31937826 A 3084 NM_001159999.1 Transcript intron_variant - - - - - - rs1947733 8:31937826 A CCDS55218.1 CCDS55218.1 Transcript intron_variant - - - - - - rs1947733 8:31937826 A 3084 NM_001160001.1 Transcript intron_variant - - - - - - rs1947733 8:31937826 A 3084 NM_013962.2 Transcript intron_variant - - - - - - rs1947733 8:31937826 A CCDS47836.1 CCDS47836.1 Transcript intron_variant - - - - - - rs1947733 8:31937826 A 3084 NM_001159995.1 Transcript intron_variant - - - - - - rs1994061 8:32048156 A 3084 NM_001159999.1 Transcript intron_variant - - - - - - rs1994061 8:32048156 A CCDS55218.1 CCDS55218.1 Transcript intron_variant - - - - - - rs1994061 8:32048156 A 3084 NM_001160001.1 Transcript intron_variant - - - - - - rs1994061 8:32048156 A 3084 NM_013962.2 Transcript intron_variant - - - - - - rs1994061 8:32048156 A CCDS47836.1 CCDS47836.1 Transcript intron_variant - - - - - - rs1994061 8:32048156 A 3084 NM_001159995.1 Transcript intron_variant - - - - - - rs7462814 8:32195119 C 3084 NM_001159999.1 Transcript intron_variant - - - - - - rs7462814 8:32195119 C CCDS55218.1 CCDS55218.1 Transcript intron_variant - - - - - - rs7462814 8:32195119 C 3084 NM_001160001.1 Transcript intron_variant - - - - - - rs7462814 8:32195119 C 3084 NM_013962.2 Transcript intron_variant - - - - - - rs7462814 8:32195119 C CCDS47836.1 CCDS47836.1 Transcript intron_variant - - - - - - rs7462814 8:32195119 C 3084 NM_001159995.1 Transcript intron_variant - - - - - - rs1685104 8:32203995 C 3084 NM_001159999.1 Transcript intron_variant - - - - - - rs1685104 8:32203995 C CCDS55218.1 CCDS55218.1 Transcript intron_variant - - - - - - rs1685104 8:32203995 C 3084 NM_001160001.1 Transcript intron_variant - - - - - - rs1685104 8:32203995 C 3084 NM_013962.2 Transcript intron_variant - - - - - - rs1685104 8:32203995 C CCDS47836.1 CCDS47836.1 Transcript intron_variant - - - - - - rs1685104 8:32203995 C 3084 NM_001159995.1 Transcript intron_variant - - - - - - rs4733340 8:32335872 G 3084 NM_001159999.1 Transcript intron_variant - - - - - - rs4733340 8:32335872 G CCDS55218.1 CCDS55218.1 Transcript intron_variant - - - - - - rs4733340 8:32335872 G 3084 NM_001160001.1 Transcript intron_variant - - - - - - rs4733340 8:32335872 G 3084 NM_013962.2 Transcript intron_variant - - - - - - rs4733340 8:32335872 G CCDS47836.1 CCDS47836.1 Transcript intron_variant - - - - - - rs4733340 8:32335872 G 3084 NM_001159995.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C CCDS55219.1 CCDS55219.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C CCDS6085.1 CCDS6085.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_013964.3 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_001160001.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_001160008.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_013962.2 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_013956.3 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_013958.3 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_001160007.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_001159995.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C ENSESTG00000020463 ENSESTT00000051322 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_001160004.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C CCDS55218.1 CCDS55218.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_001160005.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C CCDS6084.1 CCDS6084.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C CCDS47836.1 CCDS47836.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_001160002.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_001159999.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_004495.3 Transcript intron_variant - - - - - - rs2466102 8:32416572 C ENSESTG00000020463 ENSESTT00000051311 Transcript intron_variant - - - - - - rs2466102 8:32416572 C ENSESTG00000020463 ENSESTT00000051336 Transcript intron_variant - - - - - - rs2466102 8:32416572 C CCDS6086.1 CCDS6086.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_013957.3 Transcript intron_variant - - - - - - rs2466102 8:32416572 C CCDS6083.1 CCDS6083.1 Transcript intron_variant - - - - - - rs2466102 8:32416572 C 3084 NM_013960.3 Transcript intron_variant - - - - - - rs2439278 8:32467683 T CCDS55219.1 CCDS55219.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T CCDS6085.1 CCDS6085.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_013964.3 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_001160001.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_001160008.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_013962.2 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_013956.3 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_013958.3 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_001160007.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_001159995.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T ENSESTG00000020463 ENSESTT00000051322 Transcript downstream_gene_variant - - - - - - DISTANCE=4553 rs2439278 8:32467683 T 3084 NM_001160004.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T CCDS55218.1 CCDS55218.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_001160005.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T CCDS6084.1 CCDS6084.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T CCDS47836.1 CCDS47836.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_001160002.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_001159999.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T ENSESTG00000020527 ENSESTT00000051536 Transcript upstream_gene_variant - - - - - - DISTANCE=4355 rs2439278 8:32467683 T ENSESTG00000020527 ENSESTT00000051506 Transcript upstream_gene_variant - - - - - - DISTANCE=4293 rs2439278 8:32467683 T 3084 NM_004495.3 Transcript intron_variant - - - - - - rs2439278 8:32467683 T ENSESTG00000020463 ENSESTT00000051311 Transcript downstream_gene_variant - - - - - - DISTANCE=4560 rs2439278 8:32467683 T ENSESTG00000020527 ENSESTT00000051521 Transcript upstream_gene_variant - - - - - - DISTANCE=4293 rs2439278 8:32467683 T CCDS6086.1 CCDS6086.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T ENSESTG00000020527 ENSESTT00000051470 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_013957.3 Transcript intron_variant - - - - - - rs2439278 8:32467683 T CCDS6083.1 CCDS6083.1 Transcript intron_variant - - - - - - rs2439278 8:32467683 T 3084 NM_013960.3 Transcript intron_variant - - - - - - rs4733134 8:32637220 C - - - intergenic_variant - - - - - - rs4486155 8:32892638 A - - - intergenic_variant - - - - - - rs7815050 8:32971943 A - - - intergenic_variant - - - - - - rs4236726 8:33016496 T - - - intergenic_variant - - - - - - rs6990981 8:33485945 G - - - intergenic_variant - - - - - - rs6415399 8:33715374 C - - - intergenic_variant - - - - - - rs7460165 8:33721155 G - - - intergenic_variant - - - - - - rs7463919 8:33722205 T - - - intergenic_variant - - - - - - rs57324694 8:33727622 G - - - intergenic_variant - - - - - - rs6995927 8:33732191 T - - - intergenic_variant - - - - - - rs7387272 8:33735803 G - - - intergenic_variant - - - - - - rs2980330 8:33738528 G - - - intergenic_variant - - - - - - rs2959332 8:34168590 C - - - intergenic_variant - - - - - - rs13259969 8:34408261 G - - - intergenic_variant - - - - - - rs1522842 8:34564934 T - - - intergenic_variant - - - - - - rs4604425 8:34782664 G ENSESTG00000006063 ENSESTT00000015320 Transcript intron_variant - - - - - - rs2923669 8:34929714 G - - - intergenic_variant - - - - - - rs2589342 8:35412052 G 137970 NM_080872.2 Transcript intron_variant - - - - - - rs2589342 8:35412052 G CCDS6093.2 CCDS6093.2 Transcript intron_variant - - - - - - rs2589340 8:35425870 A 137970 NM_080872.2 Transcript intron_variant - - - - - - rs2589340 8:35425870 A CCDS6093.2 CCDS6093.2 Transcript intron_variant - - - - - - rs1439154 8:35440945 T 137970 NM_080872.2 Transcript intron_variant - - - - - - rs1439154 8:35440945 T CCDS6093.2 CCDS6093.2 Transcript intron_variant - - - - - - rs4543534 8:35509701 C ENSESTG00000028281 ENSESTT00000071114 Transcript intron_variant - - - - - - rs4543534 8:35509701 C 137970 NM_080872.2 Transcript intron_variant - - - - - - rs4543534 8:35509701 C CCDS6093.2 CCDS6093.2 Transcript intron_variant - - - - - - rs1436610 8:35584466 C ENSESTG00000028281 ENSESTT00000071114 Transcript intron_variant - - - - - - rs1436610 8:35584466 C 137970 NM_080872.2 Transcript intron_variant - - - - - - rs1436610 8:35584466 C ENSESTG00000028256 ENSESTT00000071100 Transcript intron_variant - - - - - - rs1436610 8:35584466 C ENSESTG00000028256 ENSESTT00000071083 Transcript intron_variant - - - - - - rs1436610 8:35584466 C CCDS6093.2 CCDS6093.2 Transcript intron_variant - - - - - - rs1561159 8:35646499 C ENSESTG00000028281 ENSESTT00000071114 Transcript 5_prime_UTR_variant 20 - - - - - rs1561159 8:35646499 C 137970 NM_080872.2 Transcript intron_variant - - - - - - rs1561159 8:35646499 C CCDS6093.2 CCDS6093.2 Transcript intron_variant - - - - - - rs7842729 8:35840411 A - - - intergenic_variant - - - - - - rs6990122 8:35846631 G - - - intergenic_variant - - - - - - rs611918 8:36191948 C - - - intergenic_variant - - - - - - rs1855623 8:36263581 C - - - intergenic_variant - - - - - - rs640521 8:36264498 A - - - intergenic_variant - - - - - - rs6468364 8:36392543 C - - - intergenic_variant - - - - - - rs6468365 8:36392566 C - - - intergenic_variant - - - - - - rs12114499 8:36463270 C - - - intergenic_variant - - - - - - rs6468376 8:36593816 A ENSESTG00000009680 ENSESTT00000024248 Transcript intron_variant - - - - - - rs10216746 8:36832166 C ENSESTG00000009603 ENSESTT00000024132 Transcript intron_variant - - - - - - rs2970726 8:36952503 T - - - intergenic_variant - - - - - - rs2460026 8:37078120 C - - - intergenic_variant - - - - - - rs548623 8:37148195 T - - - intergenic_variant - - - - - - rs390644 8:37170435 T - - - intergenic_variant - - - - - - rs459037 8:37202618 T - - - intergenic_variant - - - - - - rs12545190 8:37592257 C ENSESTG00000008519 ENSESTT00000021480 Transcript upstream_gene_variant - - - - - - DISTANCE=1895 rs12545190 8:37592257 C 11160 NM_001003791.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1840 rs12545190 8:37592257 C 11160 NM_001003790.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1940 rs12545190 8:37592257 C ENSESTG00000008519 ENSESTT00000021488 Transcript upstream_gene_variant - - - - - - DISTANCE=1895 rs12545190 8:37592257 C ENSESTG00000008519 ENSESTT00000021513 Transcript upstream_gene_variant - - - - - - DISTANCE=1947 rs12545190 8:37592257 C ENSESTG00000008502 ENSESTT00000021399 Transcript downstream_gene_variant - - - - - - DISTANCE=1432 rs12545190 8:37592257 C ENSESTG00000008519 ENSESTT00000021428 Transcript upstream_gene_variant - - - - - - DISTANCE=1862 rs12545190 8:37592257 C ENSESTG00000008519 ENSESTT00000021517 Transcript upstream_gene_variant - - - - - - DISTANCE=3194 rs12545190 8:37592257 C ENSESTG00000008519 ENSESTT00000021495 Transcript upstream_gene_variant - - - - - - DISTANCE=1895 rs12545190 8:37592257 C ENSESTG00000008519 ENSESTT00000021484 Transcript upstream_gene_variant - - - - - - DISTANCE=1895 rs12545190 8:37592257 C 11160 NM_007175.6 Transcript upstream_gene_variant - - - - - - DISTANCE=1840 rs12545190 8:37592257 C CCDS34879.1 CCDS34879.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3184 rs12545190 8:37592257 C ENSESTG00000008519 ENSESTT00000021510 Transcript upstream_gene_variant - - - - - - DISTANCE=1947 rs12545190 8:37592257 C CCDS6095.1 CCDS6095.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3184 rs28719892 8:37886813 C CCDS6100.1 CCDS6100.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1279 rs28719892 8:37886813 C ENSESTG00000000903 ENSESTT00000002190 Transcript downstream_gene_variant - - - - - - DISTANCE=1240 rs28719892 8:37886813 C 1978 NM_004095.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1207 rs28539994 8:37942199 C - - - intergenic_variant - - - - - - rs2461324 8:38398078 T ENSESTG00000000803 ENSESTT00000001954 Transcript downstream_gene_variant - - - - - - DISTANCE=3090 rs6980674 8:38755156 A ENSESTG00000000788 ENSESTT00000001945 Transcript upstream_gene_variant - - - - - - DISTANCE=3641 rs6980674 8:38755156 A ENSESTG00000000788 ENSESTT00000001941 Transcript upstream_gene_variant - - - - - - DISTANCE=3597 rs6980674 8:38755156 A ENSESTG00000000788 ENSESTT00000001951 Transcript upstream_gene_variant - - - - - - DISTANCE=3706 rs6980674 8:38755156 A 59339 NM_021623.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3597 rs6474168 8:39576872 C 8749 NM_014237.2 Transcript intron_variant - - - - - - rs6474168 8:39576872 C CCDS6113.1 CCDS6113.1 Transcript intron_variant - - - - - - rs7823916 8:40014434 T - ENSR00001390483 RegulatoryFeature regulatory_region_variant - - - - - - rs7823916 8:40014434 T 56892 NM_020130.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1607 rs7823916 8:40014434 T CCDS6115.1 CCDS6115.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3062 rs210853 8:40248422 C - - - intergenic_variant - - - - - - rs2956218 8:40307320 T - - - intergenic_variant - - - - - - rs4270951 8:40638568 C CCDS47848.1 CCDS47848.1 Transcript intron_variant - - - - - - rs4270951 8:40638568 C CCDS34885.1 CCDS34885.1 Transcript intron_variant - - - - - - rs4270951 8:40638568 C 79698 NM_001135731.1 Transcript intron_variant - - - - - - rs4270951 8:40638568 C 79698 NM_024645.2 Transcript intron_variant - - - - - - rs4270951 8:40638568 C ENSESTG00000013074 ENSESTT00000032796 Transcript intron_variant - - - - - - rs13254432 8:40677767 T - ENSR00001390565 RegulatoryFeature regulatory_region_variant - - - - - - rs13254432 8:40677767 T CCDS47848.1 CCDS47848.1 Transcript intron_variant - - - - - - rs13254432 8:40677767 T CCDS34885.1 CCDS34885.1 Transcript intron_variant - - - - - - rs13254432 8:40677767 T 79698 NM_001135731.1 Transcript intron_variant - - - - - - rs13254432 8:40677767 T 79698 NM_024645.2 Transcript intron_variant - - - - - - rs13254432 8:40677767 T ENSESTG00000013074 ENSESTT00000032796 Transcript intron_variant - - - - - - rs4493894 8:41072192 T - - - intergenic_variant - - - - - - rs2977856 8:41424250 C ENSESTG00000011696 ENSESTT00000029307 Transcript intron_variant - - - - - - rs2977847 8:41436499 T - ENSR00001390687 RegulatoryFeature regulatory_region_variant - - - - - - rs2977847 8:41436499 T ENSESTG00000011583 ENSESTT00000029032 Transcript intron_variant - - - - - - rs2977847 8:41436499 T ENSESTG00000011583 ENSESTT00000029036 Transcript intron_variant - - - - - - rs2977847 8:41436499 T 137964 NM_178819.3 Transcript intron_variant - - - - - - rs2977847 8:41436499 T ENSESTG00000011696 ENSESTT00000029307 Transcript upstream_gene_variant - - - - - - DISTANCE=612 rs2977847 8:41436499 T ENSESTG00000011583 ENSESTT00000029025 Transcript intron_variant - - - - - - rs485235 8:41516895 T - ENSR00001440751 RegulatoryFeature regulatory_region_variant - - - - - - rs485235 8:41516895 T ENSESTG00000011624 ENSESTT00000029120 Transcript upstream_gene_variant - - - - - - DISTANCE=1614 rs485235 8:41516895 T CCDS47849.1 CCDS47849.1 Transcript intron_variant - - - - - - rs485235 8:41516895 T 286 NM_020475.2 Transcript intron_variant - - - - - - rs485235 8:41516895 T 286 NM_020476.2 Transcript intron_variant - - - - - - rs485235 8:41516895 T CCDS6121.1 CCDS6121.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2089 rs485235 8:41516895 T 286 NM_001142445.1 Transcript intron_variant - - - - - - rs485235 8:41516895 T ENSESTG00000011624 ENSESTT00000029127 Transcript upstream_gene_variant - - - - - - DISTANCE=1614 rs485235 8:41516895 T 286 NM_001142446.1 Transcript intron_variant - - - - - - rs485235 8:41516895 T CCDS6119.1 CCDS6119.1 Transcript intron_variant - - - - - - rs485235 8:41516895 T ENSESTG00000011681 ENSESTT00000029287 Transcript intron_variant - - - - - - rs485235 8:41516895 T ENSESTG00000011681 ENSESTT00000029279 Transcript intron_variant - - - - - - rs485235 8:41516895 T 286 NM_020477.2 Transcript intron_variant - - - - - - rs485235 8:41516895 T CCDS55227.1 CCDS55227.1 Transcript intron_variant - - - - - - rs485235 8:41516895 T 619554 NR_030161.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1064 rs485235 8:41516895 T ENSESTG00000011681 ENSESTT00000029286 Transcript intron_variant - - - - - - rs485235 8:41516895 T ENSESTG00000011681 ENSESTT00000029291 Transcript intron_variant - - - - - - rs485235 8:41516895 T 286 NM_020480.4 Transcript intron_variant - - - - - - rs485235 8:41516895 T ENSESTG00000011618 ENSESTT00000029116 Transcript intron_variant - - - - - - rs485235 8:41516895 T ENSESTG00000011624 ENSESTT00000029124 Transcript upstream_gene_variant - - - - - - DISTANCE=1614 rs485235 8:41516895 T 286 NM_020478.4 Transcript intron_variant - - - - - - rs485235 8:41516895 T CCDS6122.1 CCDS6122.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2089 rs485235 8:41516895 T ENSESTG00000011681 ENSESTT00000029282 Transcript downstream_gene_variant - - - - - - DISTANCE=2503 rs485235 8:41516895 T CCDS6120.1 CCDS6120.1 Transcript intron_variant - - - - - - rs485235 8:41516895 T 286 NM_000037.3 Transcript intron_variant - - - - - - rs485235 8:41516895 T ENSESTG00000011681 ENSESTT00000029274 Transcript intron_variant - - - - - - rs485235 8:41516895 T ENSESTG00000011681 ENSESTT00000029295 Transcript intron_variant - - - - - - rs6474362 8:41639754 C CCDS47849.1 CCDS47849.1 Transcript intron_variant - - - - - - rs6474362 8:41639754 C ENSESTG00000011660 ENSESTT00000029205 Transcript intron_variant - - - - - - rs6474362 8:41639754 C 286 NM_020475.2 Transcript intron_variant - - - - - - rs6474362 8:41639754 C 286 NM_020476.2 Transcript intron_variant - - - - - - rs6474362 8:41639754 C CCDS6121.1 CCDS6121.1 Transcript intron_variant - - - - - - rs6474362 8:41639754 C 286 NM_001142446.1 Transcript intron_variant - - - - - - rs6474362 8:41639754 C CCDS6119.1 CCDS6119.1 Transcript intron_variant - - - - - - rs6474362 8:41639754 C 286 NM_000037.3 Transcript intron_variant - - - - - - rs6474362 8:41639754 C 286 NM_020477.2 Transcript intron_variant - - - - - - rs6474363 8:41639817 C CCDS47849.1 CCDS47849.1 Transcript intron_variant - - - - - - rs6474363 8:41639817 C ENSESTG00000011660 ENSESTT00000029205 Transcript intron_variant - - - - - - rs6474363 8:41639817 C 286 NM_020475.2 Transcript intron_variant - - - - - - rs6474363 8:41639817 C 286 NM_020476.2 Transcript intron_variant - - - - - - rs6474363 8:41639817 C CCDS6121.1 CCDS6121.1 Transcript intron_variant - - - - - - rs6474363 8:41639817 C 286 NM_001142446.1 Transcript intron_variant - - - - - - rs6474363 8:41639817 C CCDS6119.1 CCDS6119.1 Transcript intron_variant - - - - - - rs6474363 8:41639817 C 286 NM_000037.3 Transcript intron_variant - - - - - - rs6474363 8:41639817 C 286 NM_020477.2 Transcript intron_variant - - - - - - rs2976701 8:42107512 G - - - intergenic_variant - - - - - - rs7002860 8:42165000 G - ENSR00001440800 RegulatoryFeature regulatory_region_variant - - - - - - rs7002860 8:42165000 G 3551 NR_040009.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7002860 8:42165000 G ENSESTG00000013260 ENSESTT00000033306 Transcript intron_variant - - - - - - rs7002860 8:42165000 G 3551 NR_033818.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7002860 8:42165000 G ENSESTG00000013260 ENSESTT00000033310 Transcript intron_variant - - - - - - rs7002860 8:42165000 G CCDS6128.1 CCDS6128.1 Transcript intron_variant - - - - - - rs7002860 8:42165000 G 3551 NM_001190720.2 Transcript intron_variant - - - - - - rs7002860 8:42165000 G ENSESTG00000013260 ENSESTT00000033318 Transcript intron_variant - - - - - - rs7002860 8:42165000 G 3551 NR_033819.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7002860 8:42165000 G CCDS55228.1 CCDS55228.1 Transcript intron_variant - - - - - - rs7002860 8:42165000 G 3551 NM_001242778.1 Transcript intron_variant - - - - - - rs7002860 8:42165000 G 3551 NM_001556.2 Transcript intron_variant - - - - - - rs7002860 8:42165000 G CCDS56535.1 CCDS56535.1 Transcript intron_variant - - - - - - rs7007438 8:42165314 G - ENSR00001440800 RegulatoryFeature regulatory_region_variant - - - - - - rs7007438 8:42165314 G 3551 NR_040009.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7007438 8:42165314 G ENSESTG00000013260 ENSESTT00000033306 Transcript intron_variant - - - - - - rs7007438 8:42165314 G 3551 NR_033818.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7007438 8:42165314 G ENSESTG00000013260 ENSESTT00000033310 Transcript intron_variant - - - - - - rs7007438 8:42165314 G CCDS6128.1 CCDS6128.1 Transcript intron_variant - - - - - - rs7007438 8:42165314 G 3551 NM_001190720.2 Transcript intron_variant - - - - - - rs7007438 8:42165314 G ENSESTG00000013260 ENSESTT00000033318 Transcript intron_variant - - - - - - rs7007438 8:42165314 G 3551 NR_033819.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7007438 8:42165314 G CCDS55228.1 CCDS55228.1 Transcript intron_variant - - - - - - rs7007438 8:42165314 G 3551 NM_001242778.1 Transcript intron_variant - - - - - - rs7007438 8:42165314 G 3551 NM_001556.2 Transcript intron_variant - - - - - - rs7007438 8:42165314 G CCDS56535.1 CCDS56535.1 Transcript intron_variant - - - - - - rs10958711 8:42177469 G - ENSR00001440803 RegulatoryFeature regulatory_region_variant - - - - - - rs10958711 8:42177469 G 3551 NR_033818.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10958711 8:42177469 G CCDS6128.1 CCDS6128.1 Transcript intron_variant - - - - - - rs10958711 8:42177469 G ENSESTG00000013260 ENSESTT00000033318 Transcript downstream_gene_variant - - - - - - DISTANCE=81 rs10958711 8:42177469 G 3551 NR_033819.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10958711 8:42177469 G 3551 NR_040009.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10958711 8:42177469 G ENSESTG00000013260 ENSESTT00000033357 Transcript upstream_gene_variant - - - - - - DISTANCE=386 rs10958711 8:42177469 G ENSESTG00000013260 ENSESTT00000033306 Transcript downstream_gene_variant - - - - - - DISTANCE=81 rs10958711 8:42177469 G ENSESTG00000013260 ENSESTT00000033310 Transcript downstream_gene_variant - - - - - - DISTANCE=81 rs10958711 8:42177469 G 3551 NM_001190720.2 Transcript intron_variant - - - - - - rs10958711 8:42177469 G ENSESTG00000013260 ENSESTT00000033352 Transcript intron_variant - - - - - - rs10958711 8:42177469 G CCDS55228.1 CCDS55228.1 Transcript intron_variant - - - - - - rs10958711 8:42177469 G 3551 NM_001242778.1 Transcript intron_variant - - - - - - rs10958711 8:42177469 G 3551 NM_001556.2 Transcript intron_variant - - - - - - rs10958711 8:42177469 G ENSESTG00000013260 ENSESTT00000033358 Transcript upstream_gene_variant - - - - - - DISTANCE=386 rs10958711 8:42177469 G ENSESTG00000013260 ENSESTT00000033347 Transcript intron_variant - - - - - - rs10958711 8:42177469 G CCDS56535.1 CCDS56535.1 Transcript intron_variant - - - - - - rs1530849 8:42505184 C - - - intergenic_variant - - - - - - rs4737073 8:42663652 T - - - intergenic_variant - - - - - - rs4737075 8:42692110 T 55145 NM_199003.1 Transcript 3_prime_UTR_variant 1678 - - - - - rs4737075 8:42692110 T 55145 NM_018105.2 Transcript 3_prime_UTR_variant 1874 - - - - - rs4737075 8:42692110 T CCDS6136.1 CCDS6136.1 Transcript downstream_gene_variant - - - - - - DISTANCE=995 rs4737075 8:42692110 T CCDS6137.1 CCDS6137.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1279 rs1617438 8:43227674 A - - - intergenic_variant - - - - - - rs7463160 8:46936582 G - - - intergenic_variant - - - - - - rs359837 8:47236770 A - - - intergenic_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060346 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060403 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060238 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060208 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060273 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000059987 Transcript intron_variant - - - - - - rs7841397 8:48579879 A 23514 NM_001080394.2 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060144 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060389 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060296 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060423 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060107 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060099 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060221 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060327 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060311 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060416 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060313 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000059921 Transcript intron_variant - - - - - - rs7841397 8:48579879 A CCDS43737.1 CCDS43737.1 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060421 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060262 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060111 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000059971 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060258 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000059886 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060282 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060341 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000059952 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060215 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060281 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060304 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060135 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060387 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060365 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060407 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060353 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060378 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060230 Transcript intron_variant - - - - - - rs7841397 8:48579879 A ENSESTG00000023666 ENSESTT00000060297 Transcript intron_variant - - - - - - rs7008813 8:49554365 C ENSESTG00000011091 ENSESTT00000027817 Transcript intron_variant - - - - - - rs10093386 8:49706140 G - - - intergenic_variant - - - - - - rs4355781 8:50050271 T - - - intergenic_variant - - - - - - rs4300020 8:50540611 T - ENSR00001441055 RegulatoryFeature regulatory_region_variant - - - - - - rs4300020 8:50540611 T - - - intergenic_variant - - - - - - rs203955 8:50972840 T 54212 NM_018967.2 Transcript intron_variant - - - - - - rs7839015 8:51143570 T 54212 NM_018967.2 Transcript intron_variant - - - - - - rs3102075 8:51414052 G - ENSR00001391632 RegulatoryFeature regulatory_region_variant - - - - - - rs3102075 8:51414052 G CCDS6147.1 CCDS6147.1 Transcript intron_variant - - - - - - rs3102075 8:51414052 G 54212 NM_018967.2 Transcript intron_variant - - - - - - rs12544015 8:51876366 T - - - intergenic_variant - - - - - - rs4270977 8:51973570 T - - - intergenic_variant - - - - - - rs4342618 8:51973612 T - - - intergenic_variant - - - - - - rs2613280 8:53375972 C - - - intergenic_variant - - - - - - rs10808872 8:53566284 A ENSESTG00000017628 ENSESTT00000044507 Transcript intron_variant - - - - - - rs10808872 8:53566284 A 9821 NM_001083617.1 Transcript intron_variant - - - - - - rs10808872 8:53566284 A 9821 NM_014781.4 Transcript intron_variant - - - - - - rs10808872 8:53566284 A CCDS34892.1 CCDS34892.1 Transcript intron_variant - - - - - - rs10808872 8:53566284 A CCDS47856.1 CCDS47856.1 Transcript intron_variant - - - - - - rs12708142 8:53570529 A ENSESTG00000017628 ENSESTT00000044507 Transcript upstream_gene_variant - - - - - - DISTANCE=1602 rs12708142 8:53570529 A 9821 NM_001083617.1 Transcript intron_variant - - - - - - rs12708142 8:53570529 A 9821 NM_014781.4 Transcript intron_variant - - - - - - rs12708142 8:53570529 A CCDS34892.1 CCDS34892.1 Transcript intron_variant - - - - - - rs12708142 8:53570529 A CCDS47856.1 CCDS47856.1 Transcript intron_variant - - - - - - rs13265506 8:54158924 A ENSESTG00000033256 ENSESTT00000084021 Transcript intron_variant - - - - - - rs13265506 8:54158924 A ENSESTG00000033256 ENSESTT00000084014 Transcript intron_variant - - - - - - rs13265506 8:54158924 A 4986 NM_000912.3 Transcript intron_variant - - - - - - rs13265506 8:54158924 A CCDS6152.1 CCDS6152.1 Transcript intron_variant - - - - - - rs1466436 8:54460934 A - - - intergenic_variant - - - - - - rs7821878 8:54675960 A 51606 NM_213620.2 Transcript intron_variant - - - - - - rs7821878 8:54675960 A CCDS6153.1 CCDS6153.1 Transcript intron_variant - - - - - - rs7821878 8:54675960 A ENSESTG00000033197 ENSESTT00000083955 Transcript intron_variant - - - - - - rs7821878 8:54675960 A ENSESTG00000033197 ENSESTT00000083952 Transcript intron_variant - - - - - - rs7821878 8:54675960 A 51606 NM_015941.3 Transcript intron_variant - - - - - - rs7821878 8:54675960 A CCDS6154.1 CCDS6154.1 Transcript intron_variant - - - - - - rs7821878 8:54675960 A 51606 NM_213619.2 Transcript intron_variant - - - - - - rs1483543 8:54748000 C 51606 NM_213620.2 Transcript intron_variant - - - - - - rs1483543 8:54748000 C ENSESTG00000033197 ENSESTT00000083932 Transcript intron_variant - - - - - - rs1483543 8:54748000 C CCDS6153.1 CCDS6153.1 Transcript intron_variant - - - - - - rs1483543 8:54748000 C CCDS6154.1 CCDS6154.1 Transcript intron_variant - - - - - - rs1483543 8:54748000 C 51606 NM_213619.2 Transcript intron_variant - - - - - - rs1483543 8:54748000 C ENSESTG00000033197 ENSESTT00000083925 Transcript intron_variant - - - - - - rs1483543 8:54748000 C ENSESTG00000033197 ENSESTT00000083881 Transcript intron_variant - - - - - - rs1483543 8:54748000 C 51606 NM_015941.3 Transcript intron_variant - - - - - - rs461406 8:55126391 G - - - intergenic_variant - - - - - - rs10094089 8:55187307 C - - - intergenic_variant - - - - - - rs7823891 8:55401464 C - - - intergenic_variant - - - - - - rs6473949 8:55529487 A ENSESTG00000028915 ENSESTT00000072831 Transcript intron_variant - - - - - - rs6473949 8:55529487 A CCDS6160.1 CCDS6160.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4040 rs6473949 8:55529487 A ENSESTG00000028915 ENSESTT00000072873 Transcript intron_variant - - - - - - rs6473949 8:55529487 A ENSESTG00000028915 ENSESTT00000072842 Transcript intron_variant - - - - - - rs6473949 8:55529487 A 6101 NM_006269.1 Transcript intron_variant - - - - - - rs4351396 8:55912648 T ENSESTG00000008641 ENSESTT00000021721 Transcript upstream_gene_variant - - - - - - DISTANCE=4154 rs10958447 8:56068576 A CCDS34893.1 CCDS34893.1 Transcript intron_variant - - - - - - rs10958447 8:56068576 A ENSESTG00000008651 ENSESTT00000021726 Transcript intron_variant - - - - - - rs10958447 8:56068576 A 114786 NM_052898.1 Transcript intron_variant - - - - - - rs4737968 8:56155587 T CCDS34893.1 CCDS34893.1 Transcript intron_variant - - - - - - rs4737968 8:56155587 T ENSESTG00000008651 ENSESTT00000021726 Transcript intron_variant - - - - - - rs4737968 8:56155587 T 114786 NM_052898.1 Transcript intron_variant - - - - - - rs4379423 8:56223169 G CCDS34893.1 CCDS34893.1 Transcript intron_variant - - - - - - rs4379423 8:56223169 G ENSESTG00000008651 ENSESTT00000021726 Transcript intron_variant - - - - - - rs4379423 8:56223169 G 114786 NM_052898.1 Transcript intron_variant - - - - - - rs2979059 8:56299419 A CCDS34893.1 CCDS34893.1 Transcript intron_variant - - - - - - rs2979059 8:56299419 A 114786 NM_052898.1 Transcript intron_variant - - - - - - rs2975946 8:56306959 A CCDS34893.1 CCDS34893.1 Transcript intron_variant - - - - - - rs2975946 8:56306959 A 114786 NM_052898.1 Transcript intron_variant - - - - - - rs2928999 8:56331256 C CCDS34893.1 CCDS34893.1 Transcript intron_variant - - - - - - rs2928999 8:56331256 C 114786 NM_052898.1 Transcript intron_variant - - - - - - rs2929053 8:56359428 C CCDS34893.1 CCDS34893.1 Transcript intron_variant - - - - - - rs2929053 8:56359428 C 114786 NM_052898.1 Transcript intron_variant - - - - - - rs2929053 8:56359428 C 100133234 NR_027765.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2329 rs2975980 8:56366502 C CCDS34893.1 CCDS34893.1 Transcript intron_variant - - - - - - rs2975980 8:56366502 C 114786 NM_052898.1 Transcript intron_variant - - - - - - rs2975980 8:56366502 C 100133234 NR_027765.1 Transcript non_coding_exon_variant,nc_transcript_variant 1380 - - - - - rs2939653 8:56379974 A CCDS34893.1 CCDS34893.1 Transcript intron_variant - - - - - - rs2939653 8:56379974 A 114786 NM_052898.1 Transcript intron_variant - - - - - - rs4521734 8:56493671 T - - - intergenic_variant - - - - - - rs13272229 8:56498751 G - - - intergenic_variant - - - - - - rs6474003 8:56517724 T - - - intergenic_variant - - - - - - rs925448 8:56919335 C - ENSR00001392263 RegulatoryFeature regulatory_region_variant - - - - - - rs925448 8:56919335 C CCDS47859.1 CCDS47859.1 Transcript intron_variant - - - - - - rs925448 8:56919335 C 4067 NM_002350.3 Transcript intron_variant - - - - - - rs925448 8:56919335 C ENSESTG00000011924 ENSESTT00000029928 Transcript intron_variant - - - - - - rs925448 8:56919335 C 4067 NM_001111097.2 Transcript intron_variant - - - - - - rs925448 8:56919335 C ENSESTG00000011924 ENSESTT00000029932 Transcript intron_variant - - - - - - rs925448 8:56919335 C CCDS6162.1 CCDS6162.1 Transcript intron_variant - - - - - - rs925448 8:56919335 C ENSESTG00000012109 ENSESTT00000030306 Transcript intron_variant - - - - - - rs6987263 8:57086205 T - ENSR00001392297 RegulatoryFeature regulatory_region_variant - - - - - - rs6987263 8:57086205 T 5324 NM_001114635.1 Transcript intron_variant - - - - - - rs6987263 8:57086205 T 5324 NM_002655.2 Transcript intron_variant - - - - - - rs6987263 8:57086205 T ENSESTG00000012080 ENSESTT00000030231 Transcript intron_variant - - - - - - rs6987263 8:57086205 T 5324 NM_001114634.1 Transcript intron_variant - - - - - - rs6987263 8:57086205 T ENSESTG00000012080 ENSESTT00000030233 Transcript intron_variant - - - - - - rs7461695 8:57210670 G ENSESTG00000012051 ENSESTT00000030204 Transcript downstream_gene_variant - - - - - - DISTANCE=3116 rs7461695 8:57210670 G 195814 NM_138969.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1900 rs7461695 8:57210670 G CCDS6167.1 CCDS6167.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3369 rs1946774 8:57293523 G ENSESTG00000012049 ENSESTT00000030165 Transcript intron_variant - - - - - - rs2119387 8:57440308 G ENSESTG00000012027 ENSESTT00000030124 Transcript intron_variant - - - - - - rs2119387 8:57440308 G ENSESTG00000012027 ENSESTT00000030121 Transcript intron_variant - - - - - - rs2119387 8:57440308 G ENSESTG00000012027 ENSESTT00000030119 Transcript intron_variant - - - - - - rs2119387 8:57440308 G 100507632 NR_038236.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs353755 8:57675775 C - - - intergenic_variant - - - - - - rs4738587 8:58286000 C - - - intergenic_variant - - - - - - rs10957000 8:58314549 T - - - intergenic_variant - - - - - - rs2122710 8:58392391 T - - - intergenic_variant - - - - - - rs4483144 8:59184565 G ENSESTG00000001807 ENSESTT00000004434 Transcript 5_prime_UTR_variant 98 - - - - - rs7842881 8:60803074 C - - - intergenic_variant - - - - - - rs2326563 8:61432323 T CCDS56537.1 CCDS56537.1 Transcript intron_variant - - - - - - rs2326563 8:61432323 T 5862 NM_001242644.1 Transcript intron_variant - - - - - - rs2326563 8:61432323 T 5862 NM_002865.2 Transcript intron_variant - - - - - - rs2326563 8:61432323 T CCDS6175.1 CCDS6175.1 Transcript intron_variant - - - - - - rs2326563 8:61432323 T ENSESTG00000033133 ENSESTT00000083811 Transcript intron_variant - - - - - - rs7464309 8:61915077 G - - - intergenic_variant - - - - - - rs1288035 8:61989557 T - ENSR00001392933 RegulatoryFeature regulatory_region_variant - - - - - - rs1288035 8:61989557 T ENSESTG00000016699 ENSESTT00000041874 Transcript intron_variant - - - - - - rs1988953 8:62813204 C - - - intergenic_variant - - - - - - rs344297 8:62863838 T - - - intergenic_variant - - - - - - rs344246 8:62950945 T - - - intergenic_variant - - - - - - rs7013507 8:63037358 A ENSESTG00000008066 ENSESTT00000020389 Transcript downstream_gene_variant - - - - - - DISTANCE=4902 rs4738942 8:63116562 G - - - intergenic_variant - - - - - - rs1384682 8:63144343 T - - - intergenic_variant - - - - - - rs2351948 8:63249979 A CCDS55239.1 CCDS55239.1 Transcript intron_variant - - - - - - rs2351948 8:63249979 A 286183 NM_173688.2 Transcript intron_variant - - - - - - rs2351658 8:63308902 A CCDS55239.1 CCDS55239.1 Transcript intron_variant - - - - - - rs2351658 8:63308902 A 286183 NM_173688.2 Transcript intron_variant - - - - - - rs7010101 8:63796515 A CCDS55239.1 CCDS55239.1 Transcript intron_variant - - - - - - rs7010101 8:63796515 A 286183 NM_173688.2 Transcript intron_variant - - - - - - rs791173 8:64691146 G ENSESTG00000024974 ENSESTT00000063028 Transcript missense_variant 529 62 21 H/R cAc/cGc - rs791173 8:64691146 G 286184 NR_038875.1 Transcript non_coding_exon_variant,nc_transcript_variant 557 - - - - - rs1025164 8:64824533 A - - - intergenic_variant - - - - - - rs1244632 8:65325428 T - - - intergenic_variant - - - - - - rs4236935 8:65630694 C CCDS6180.1 CCDS6180.1 Transcript intron_variant - - - - - - rs4236935 8:65630694 C ENSESTG00000022424 ENSESTT00000056632 Transcript intron_variant - - - - - - rs4236935 8:65630694 C 9420 NM_004820.3 Transcript intron_variant - - - - - - rs4236935 8:65630694 C ENSESTG00000022235 ENSESTT00000056154 Transcript intron_variant - - - - - - rs7841215 8:65759959 T - - - intergenic_variant - - - - - - rs12543877 8:65874561 A - - - intergenic_variant - - - - - - rs10103173 8:66194190 C - - - intergenic_variant - - - - - - rs13265307 8:66255155 C - - - intergenic_variant - - - - - - rs10957360 8:66514506 G CCDS6181.1 CCDS6181.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2123 rs10957360 8:66514506 G 55156 NM_018120.4 Transcript downstream_gene_variant - - - - - - DISTANCE=185 rs10957360 8:66514506 G ENSESTG00000032576 ENSESTT00000082311 Transcript downstream_gene_variant - - - - - - DISTANCE=2017 rs4737760 8:66845335 G - - - intergenic_variant - - - - - - rs10095225 8:66960549 C 85479 NM_033105.4 Transcript intron_variant - - - - - - rs10095225 8:66960549 C CCDS6183.1 CCDS6183.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3234 rs4737231 8:67363335 T ENSESTG00000029124 ENSESTT00000073489 Transcript intron_variant - - - - - - rs4737231 8:67363335 T ENSESTG00000029124 ENSESTT00000073476 Transcript intron_variant - - - - - - rs4737231 8:67363335 T ENSESTG00000029124 ENSESTT00000073433 Transcript intron_variant - - - - - - rs4737231 8:67363335 T CCDS6190.2 CCDS6190.2 Transcript intron_variant - - - - - - rs4737231 8:67363335 T ENSESTG00000029124 ENSESTT00000073560 Transcript upstream_gene_variant - - - - - - DISTANCE=2782 rs4737231 8:67363335 T ENSESTG00000029124 ENSESTT00000073579 Transcript upstream_gene_variant - - - - - - DISTANCE=2782 rs4737231 8:67363335 T ENSESTG00000029124 ENSESTT00000073441 Transcript intron_variant - - - - - - rs4737231 8:67363335 T 137872 NM_144650.2 Transcript intron_variant - - - - - - rs10089495 8:67971819 T CCDS6198.1 CCDS6198.1 Transcript intron_variant - - - - - - rs10089495 8:67971819 T 10987 NM_006837.2 Transcript intron_variant - - - - - - rs10089495 8:67971819 T ENSESTG00000012275 ENSESTT00000030833 Transcript intron_variant - - - - - - rs10089495 8:67971819 T ENSESTG00000012128 ENSESTT00000030379 Transcript upstream_gene_variant - - - - - - DISTANCE=2842 rs10089495 8:67971819 T CCDS43744.1 CCDS43744.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4815 rs10089495 8:67971819 T ENSESTG00000012128 ENSESTT00000030342 Transcript upstream_gene_variant - - - - - - DISTANCE=2833 rs10089495 8:67971819 T ENSESTG00000012128 ENSESTT00000030387 Transcript upstream_gene_variant - - - - - - DISTANCE=4849 rs10089495 8:67971819 T ENSESTG00000012275 ENSESTT00000030809 Transcript intron_variant - - - - - - rs10089495 8:67971819 T 79848 NM_024790.6 Transcript upstream_gene_variant - - - - - - DISTANCE=4784 rs10957386 8:68348487 G CCDS6200.1 CCDS6200.1 Transcript intron_variant - - - - - - rs10957386 8:68348487 G 57094 NM_020361.4 Transcript intron_variant - - - - - - rs1564554 8:68611006 T CCDS6200.1 CCDS6200.1 Transcript intron_variant - - - - - - rs1564554 8:68611006 T 57094 NM_020361.4 Transcript intron_variant - - - - - - rs1564554 8:68611006 T ENSESTG00000012194 ENSESTT00000030496 Transcript intron_variant - - - - - - rs2623814 8:68703691 C - - - intergenic_variant - - - - - - rs6987531 8:68856803 A - - - intergenic_variant - - - - - - rs2571371 8:68980752 A CCDS6201.1 CCDS6201.1 Transcript intron_variant - - - - - - rs2571371 8:68980752 A 80243 NM_024870.2 Transcript intron_variant - - - - - - rs2571371 8:68980752 A ENSESTG00000026103 ENSESTT00000065918 Transcript upstream_gene_variant - - - - - - DISTANCE=3977 rs2571371 8:68980752 A ENSESTG00000026103 ENSESTT00000065900 Transcript intron_variant - - - - - - rs2571371 8:68980752 A 80243 NM_025170.4 Transcript intron_variant - - - - - - rs7001451 8:69399724 G ENSESTG00000026214 ENSESTT00000066165 Transcript intron_variant - - - - - - rs7001451 8:69399724 G ENSESTG00000026214 ENSESTT00000066190 Transcript intron_variant - - - - - - rs7001451 8:69399724 G ENSESTG00000026214 ENSESTT00000066150 Transcript intron_variant - - - - - - rs7001451 8:69399724 G 116328 NM_001195639.1 Transcript intron_variant - - - - - - rs7001451 8:69399724 G CCDS6203.2 CCDS6203.2 Transcript intron_variant - - - - - - rs7001451 8:69399724 G ENSESTG00000026214 ENSESTT00000066157 Transcript intron_variant - - - - - - rs7001451 8:69399724 G 116328 NM_052958.2 Transcript intron_variant - - - - - - rs7001451 8:69399724 G ENSESTG00000026214 ENSESTT00000066159 Transcript intron_variant - - - - - - rs7001451 8:69399724 G ENSESTG00000026214 ENSESTT00000066172 Transcript intron_variant - - - - - - rs7001906 8:69399746 A ENSESTG00000026214 ENSESTT00000066165 Transcript intron_variant - - - - - - rs7001906 8:69399746 A ENSESTG00000026214 ENSESTT00000066190 Transcript intron_variant - - - - - - rs7001906 8:69399746 A ENSESTG00000026214 ENSESTT00000066150 Transcript intron_variant - - - - - - rs7001906 8:69399746 A 116328 NM_001195639.1 Transcript intron_variant - - - - - - rs7001906 8:69399746 A CCDS6203.2 CCDS6203.2 Transcript intron_variant - - - - - - rs7001906 8:69399746 A ENSESTG00000026214 ENSESTT00000066157 Transcript intron_variant - - - - - - rs7001906 8:69399746 A 116328 NM_052958.2 Transcript intron_variant - - - - - - rs7001906 8:69399746 A ENSESTG00000026214 ENSESTT00000066159 Transcript intron_variant - - - - - - rs7001906 8:69399746 A ENSESTG00000026214 ENSESTT00000066172 Transcript intron_variant - - - - - - rs7009743 8:69443554 G ENSESTG00000026214 ENSESTT00000066165 Transcript intron_variant - - - - - - rs7009743 8:69443554 G ENSESTG00000026214 ENSESTT00000066190 Transcript intron_variant - - - - - - rs7009743 8:69443554 G ENSESTG00000026214 ENSESTT00000066150 Transcript intron_variant - - - - - - rs7009743 8:69443554 G 116328 NM_001195639.1 Transcript intron_variant - - - - - - rs7009743 8:69443554 G CCDS6203.2 CCDS6203.2 Transcript intron_variant - - - - - - rs7009743 8:69443554 G ENSESTG00000026214 ENSESTT00000066157 Transcript intron_variant - - - - - - rs7009743 8:69443554 G 116328 NM_052958.2 Transcript intron_variant - - - - - - rs7009743 8:69443554 G ENSESTG00000026214 ENSESTT00000066159 Transcript intron_variant - - - - - - rs6982047 8:69661774 C ENSESTG00000026214 ENSESTT00000066190 Transcript intron_variant - - - - - - rs6982047 8:69661774 C ENSESTG00000026214 ENSESTT00000066150 Transcript intron_variant - - - - - - rs6982047 8:69661774 C CCDS6203.2 CCDS6203.2 Transcript intron_variant - - - - - - rs6982047 8:69661774 C ENSESTG00000026214 ENSESTT00000066211 Transcript intron_variant - - - - - - rs6982047 8:69661774 C ENSESTG00000026214 ENSESTT00000066239 Transcript intron_variant - - - - - - rs6982047 8:69661774 C ENSESTG00000026214 ENSESTT00000066157 Transcript intron_variant - - - - - - rs6982047 8:69661774 C 116328 NM_052958.2 Transcript intron_variant - - - - - - rs6472418 8:69663684 C - ENSR00001393767 RegulatoryFeature regulatory_region_variant - - - - - - rs6472418 8:69663684 C ENSESTG00000026214 ENSESTT00000066190 Transcript intron_variant - - - - - - rs6472418 8:69663684 C ENSESTG00000026214 ENSESTT00000066150 Transcript intron_variant - - - - - - rs6472418 8:69663684 C CCDS6203.2 CCDS6203.2 Transcript intron_variant - - - - - - rs6472418 8:69663684 C ENSESTG00000026214 ENSESTT00000066211 Transcript intron_variant - - - - - - rs6472418 8:69663684 C ENSESTG00000026214 ENSESTT00000066239 Transcript intron_variant - - - - - - rs6472418 8:69663684 C ENSESTG00000026214 ENSESTT00000066157 Transcript intron_variant - - - - - - rs6472418 8:69663684 C 116328 NM_052958.2 Transcript intron_variant - - - - - - rs2981039 8:69991001 T - ENSR00001441962 RegulatoryFeature regulatory_region_variant - - - - - - rs2981039 8:69991001 T 100505718 NR_039986.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2981039 8:69991001 T ENSESTG00000033365 ENSESTT00000084251 Transcript intron_variant - - - - - - rs6415609 8:70069500 T - - - intergenic_variant - - - - - - rs7815728 8:70075854 T - - - intergenic_variant - - - - - - rs580398 8:70075907 A - - - intergenic_variant - - - - - - rs1822149 8:70335926 C ENSESTG00000033345 ENSESTT00000084203 Transcript downstream_gene_variant - - - - - - DISTANCE=1734 rs1372152 8:70472566 T 23213 NM_015170.2 Transcript intron_variant - - - - - - rs1372152 8:70472566 T ENSESTG00000033191 ENSESTT00000083949 Transcript upstream_gene_variant - - - - - - DISTANCE=2477 rs1372152 8:70472566 T CCDS6204.1 CCDS6204.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3645 rs1372152 8:70472566 T 23213 NM_001128204.1 Transcript intron_variant - - - - - - rs1372152 8:70472566 T ENSESTG00000033191 ENSESTT00000083942 Transcript intron_variant - - - - - - rs1372152 8:70472566 T 23213 NM_001128205.1 Transcript intron_variant - - - - - - rs1372152 8:70472566 T ENSESTG00000033191 ENSESTT00000083969 Transcript upstream_gene_variant - - - - - - DISTANCE=2482 rs1372152 8:70472566 T ENSESTG00000033343 ENSESTT00000084193 Transcript intron_variant - - - - - - rs1372152 8:70472566 T 23213 NM_001128206.1 Transcript intron_variant - - - - - - rs1372152 8:70472566 T ENSESTG00000033191 ENSESTT00000083882 Transcript intron_variant - - - - - - rs11990615 8:70523682 C 23213 NM_015170.2 Transcript intron_variant - - - - - - rs11990615 8:70523682 C CCDS6204.1 CCDS6204.1 Transcript intron_variant - - - - - - rs11990615 8:70523682 C 23213 NM_001128204.1 Transcript intron_variant - - - - - - rs11990615 8:70523682 C 23213 NM_001128205.1 Transcript intron_variant - - - - - - rs11990615 8:70523682 C ENSESTG00000033191 ENSESTT00000083969 Transcript intron_variant - - - - - - rs11990615 8:70523682 C 23213 NM_001128206.1 Transcript intron_variant - - - - - - rs11990615 8:70523682 C ENSESTG00000033343 ENSESTT00000084193 Transcript intron_variant - - - - - - rs11990615 8:70523682 C ENSESTG00000033191 ENSESTT00000083882 Transcript intron_variant - - - - - - rs2959564 8:70624116 T CCDS55243.1 CCDS55243.1 Transcript intron_variant - - - - - - rs2959564 8:70624116 T 81796 NM_030958.2 Transcript intron_variant - - - - - - rs2959564 8:70624116 T CCDS6205.1 CCDS6205.1 Transcript intron_variant - - - - - - rs2959564 8:70624116 T 81796 NM_001146008.1 Transcript intron_variant - - - - - - rs2959564 8:70624116 T CCDS55242.1 CCDS55242.1 Transcript intron_variant - - - - - - rs2959564 8:70624116 T 81796 NM_001146009.1 Transcript intron_variant - - - - - - rs2959564 8:70624116 T ENSESTG00000033283 ENSESTT00000084160 Transcript intron_variant - - - - - - rs268609 8:71607022 G ENSESTG00000017859 ENSESTT00000045005 Transcript intron_variant - - - - - - rs268609 8:71607022 G CCDS34905.1 CCDS34905.1 Transcript intron_variant - - - - - - rs268609 8:71607022 G 389668 NM_001011720.1 Transcript intron_variant - - - - - - rs6472565 8:71993690 G - - - intergenic_variant - - - - - - rs1424872 8:72533245 T - - - intergenic_variant - - - - - - rs4738391 8:74572714 G CCDS55246.1 CCDS55246.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G CCDS55247.1 CCDS55247.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G 27067 NM_001164380.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G ENSESTG00000021960 ENSESTT00000055551 Transcript intron_variant - - - - - - rs4738391 8:74572714 G 27067 NM_001164385.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G ENSESTG00000021960 ENSESTT00000055610 Transcript intron_variant - - - - - - rs4738391 8:74572714 G ENSESTG00000021960 ENSESTT00000055531 Transcript intron_variant - - - - - - rs4738391 8:74572714 G ENSESTG00000021960 ENSESTT00000055623 Transcript intron_variant - - - - - - rs4738391 8:74572714 G 27067 NM_001164384.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G 27067 NM_001164383.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G ENSESTG00000021960 ENSESTT00000055626 Transcript intron_variant - - - - - - rs4738391 8:74572714 G 27067 NM_001164381.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G 27067 NM_014393.2 Transcript intron_variant - - - - - - rs4738391 8:74572714 G ENSESTG00000021960 ENSESTT00000055482 Transcript intron_variant - - - - - - rs4738391 8:74572714 G 27067 NM_001164382.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G CCDS6214.1 CCDS6214.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G ENSESTG00000021960 ENSESTT00000055496 Transcript intron_variant - - - - - - rs4738391 8:74572714 G CCDS55248.1 CCDS55248.1 Transcript intron_variant - - - - - - rs4738391 8:74572714 G CCDS55245.1 CCDS55245.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G CCDS55246.1 CCDS55246.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G CCDS55247.1 CCDS55247.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055568 Transcript downstream_gene_variant - - - - - - DISTANCE=2610 rs7010119 8:74598376 G 27067 NM_001164380.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055551 Transcript intron_variant - - - - - - rs7010119 8:74598376 G 27067 NM_001164385.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055610 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055531 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055623 Transcript intron_variant - - - - - - rs7010119 8:74598376 G 27067 NM_001164384.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055585 Transcript downstream_gene_variant - - - - - - DISTANCE=2594 rs7010119 8:74598376 G 27067 NM_001164383.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055520 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055626 Transcript intron_variant - - - - - - rs7010119 8:74598376 G 27067 NM_001164381.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G 27067 NM_014393.2 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055482 Transcript intron_variant - - - - - - rs7010119 8:74598376 G 27067 NM_001164382.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055219 Transcript downstream_gene_variant - - - - - - DISTANCE=2562 rs7010119 8:74598376 G CCDS6214.1 CCDS6214.1 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055496 Transcript intron_variant - - - - - - rs7010119 8:74598376 G ENSESTG00000021960 ENSESTT00000055273 Transcript downstream_gene_variant - - - - - - DISTANCE=2531 rs7010119 8:74598376 G CCDS55248.1 CCDS55248.1 Transcript intron_variant - - - - - - rs4738395 8:74815459 C - - - intergenic_variant - - - - - - rs7828201 8:75262798 C - ENSR00001394503 RegulatoryFeature regulatory_region_variant - - - - - - rs7828201 8:75262798 C 54332 NM_018972.2 Transcript synonymous_variant 181 102 34 S tcG/tcC - rs7828201 8:75262798 C CCDS47877.1 CCDS47877.1 Transcript upstream_gene_variant - - - - - - DISTANCE=798 rs7828201 8:75262798 C ENSESTG00000025491 ENSESTT00000064351 Transcript 5_prime_UTR_variant 120 - - - - - rs7828201 8:75262798 C 54332 NM_001040875.2 Transcript intron_variant - - - - - - rs7828201 8:75262798 C 54332 NR_046346.1 Transcript non_coding_exon_variant,nc_transcript_variant 181 - - - - - rs7828201 8:75262798 C CCDS34911.1 CCDS34911.1 Transcript synonymous_variant 102 102 34 S tcG/tcC - rs7828201 8:75262798 C ENSESTG00000025491 ENSESTT00000064306 Transcript synonymous_variant 171 102 34 S tcG/tcC - rs4738454 8:75291536 C - - - intergenic_variant - - - - - - rs10957709 8:75293495 C - - - intergenic_variant - - - - - - rs4520151 8:75294185 C - - - intergenic_variant - - - - - - rs10957711 8:75304026 A - - - intergenic_variant - - - - - - rs10755956 8:75305736 A - - - intergenic_variant - - - - - - rs6472850 8:75335735 A - - - intergenic_variant - - - - - - rs6472852 8:75339080 C - - - intergenic_variant - - - - - - rs10808800 8:75353080 G - - - intergenic_variant - - - - - - rs6998004 8:75353344 G - - - intergenic_variant - - - - - - rs4645551 8:75354169 C - - - intergenic_variant - - - - - - rs4554458 8:75354265 C - - - intergenic_variant - - - - - - rs4357276 8:75355382 G - - - intergenic_variant - - - - - - rs7014233 8:75356387 T - - - intergenic_variant - - - - - - rs4269535 8:75356731 G - - - intergenic_variant - - - - - - rs4418332 8:75358332 T - - - intergenic_variant - - - - - - rs4308721 8:75360817 C - - - intergenic_variant - - - - - - rs7816881 8:75361053 G - - - intergenic_variant - - - - - - rs7816889 8:75361062 G - - - intergenic_variant - - - - - - rs7010451 8:75361698 G - - - intergenic_variant - - - - - - rs10957720 8:75369444 A - - - intergenic_variant - - - - - - rs10103151 8:75370314 C - - - intergenic_variant - - - - - - rs10755957 8:75372870 C - - - intergenic_variant - - - - - - rs10755958 8:75372896 A - - - intergenic_variant - - - - - - rs10957721 8:75373187 G - - - intergenic_variant - - - - - - rs10100554 8:75373401 T - - - intergenic_variant - - - - - - rs10100273 8:75373447 G - - - intergenic_variant - - - - - - rs4386974 8:75374986 T - - - intergenic_variant - - - - - - rs4538867 8:75375454 A - - - intergenic_variant - - - - - - rs4573265 8:75375520 T - - - intergenic_variant - - - - - - rs6999775 8:75375908 A - - - intergenic_variant - - - - - - rs6999568 8:75376047 T - - - intergenic_variant - - - - - - rs7004069 8:75376503 G - - - intergenic_variant - - - - - - rs12541099 8:75403218 A - - - intergenic_variant - - - - - - rs2383927 8:75854671 A - - - intergenic_variant - - - - - - rs2954868 8:75862513 T - - - intergenic_variant - - - - - - rs1378618 8:76056638 T - - - intergenic_variant - - - - - - rs2922760 8:76541008 A - - - intergenic_variant - - - - - - rs2941442 8:76552393 G - - - intergenic_variant - - - - - - rs4476993 8:77346490 C - - - intergenic_variant - - - - - - rs2570597 8:77632772 T 79776 NM_024721.4 Transcript intron_variant - - - - - - rs2570597 8:77632772 T CCDS47878.2 CCDS47878.2 Transcript intron_variant - - - - - - rs1988907 8:78284978 C - - - intergenic_variant - - - - - - rs389482 8:78522038 A - - - intergenic_variant - - - - - - rs4041611 8:78610082 T - - - intergenic_variant - - - - - - rs1589215 8:78739108 G - - - intergenic_variant - - - - - - rs1607532 8:78740177 G - - - intergenic_variant - - - - - - rs1850817 8:78742496 G - - - intergenic_variant - - - - - - rs7821393 8:78911664 C - - - intergenic_variant - - - - - - rs2587154 8:79735883 G ENSESTG00000002275 ENSESTT00000005685 Transcript intron_variant - - - - - - rs2717542 8:79769916 G ENSESTG00000002275 ENSESTT00000005685 Transcript intron_variant - - - - - - rs2433586 8:81484901 G - - - intergenic_variant - - - - - - rs2433585 8:81485063 G - - - intergenic_variant - - - - - - rs6992197 8:81912288 A 55824 NM_018440.3 Transcript intron_variant - - - - - - rs7831015 8:81949316 A - ENSR00001442592 RegulatoryFeature regulatory_region_variant - - - - - - rs7831015 8:81949316 A ENSESTG00000013518 ENSESTT00000033847 Transcript intron_variant - - - - - - rs7831015 8:81949316 A 55824 NM_018440.3 Transcript intron_variant - - - - - - rs2556596 8:82507002 A - - - intergenic_variant - - - - - - rs1842099 8:83191355 C - - - intergenic_variant - - - - - - rs1031880 8:83218747 T - - - intergenic_variant - - - - - - rs796479 8:83500331 G - - - intergenic_variant - - - - - - rs7817798 8:83639850 C - - - intergenic_variant - - - - - - rs2140818 8:83647783 G - - - intergenic_variant - - - - - - rs7842243 8:83732811 C - - - intergenic_variant - - - - - - rs9772351 8:83912181 C - - - intergenic_variant - - - - - - rs7004443 8:84351019 A ENSESTG00000024493 ENSESTT00000061909 Transcript upstream_gene_variant - - - - - - DISTANCE=2776 rs4518662 8:84617187 G - - - intergenic_variant - - - - - - rs1348219 8:84935189 T - - - intergenic_variant - - - - - - rs4740007 8:85225358 G CCDS55252.1 CCDS55252.1 Transcript intron_variant - - - - - - rs4740007 8:85225358 G 138046 NM_001100393.1 Transcript intron_variant - - - - - - rs4740007 8:85225358 G 138046 NM_001100392.1 Transcript intron_variant - - - - - - rs4740007 8:85225358 G 138046 NM_173848.5 Transcript intron_variant - - - - - - rs4740007 8:85225358 G 138046 NM_001100391.1 Transcript intron_variant - - - - - - rs1681332 8:85463893 G CCDS55252.1 CCDS55252.1 Transcript intron_variant - - - - - - rs1681332 8:85463893 G 138046 NM_001100393.1 Transcript intron_variant - - - - - - rs1681332 8:85463893 G 138046 NM_001100392.1 Transcript intron_variant - - - - - - rs1681332 8:85463893 G CCDS55253.1 CCDS55253.1 Transcript intron_variant - - - - - - rs1681332 8:85463893 G 138046 NM_173848.5 Transcript intron_variant - - - - - - rs1681332 8:85463893 G 138046 NM_001100391.1 Transcript intron_variant - - - - - - rs144109619 8:85918105 G - - - intergenic_variant - - - - - - rs13258189 8:86175293 A 377677 NM_198584.2 Transcript intron_variant - - - - - - rs13258189 8:86175293 A CCDS6236.1 CCDS6236.1 Transcript intron_variant - - - - - - rs13258189 8:86175293 A ENSESTG00000003168 ENSESTT00000007872 Transcript intron_variant - - - - - - rs4960943 8:87056401 T - ENSR00001442737 RegulatoryFeature regulatory_region_variant - - - - - - rs4960943 8:87056401 T CCDS6240.1 CCDS6240.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4290 rs4960943 8:87056401 T 85481 NM_033126.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4290 rs4509296 8:87069181 G CCDS6240.1 CCDS6240.1 Transcript intron_variant - - - - - - rs4509296 8:87069181 G 85481 NM_033126.1 Transcript intron_variant - - - - - - rs2626323 8:87145155 T 245972 NM_152565.1 Transcript intron_variant - - - - - - rs2626323 8:87145155 T CCDS6241.1 CCDS6241.1 Transcript intron_variant - - - - - - rs2626323 8:87145155 T ENSESTG00000013250 ENSESTT00000033225 Transcript intron_variant - - - - - - rs2626323 8:87145155 T ENSESTG00000013122 ENSESTT00000032888 Transcript intron_variant - - - - - - rs2626323 8:87145155 T ENSESTG00000013122 ENSESTT00000032890 Transcript intron_variant - - - - - - rs2954343 8:87236247 T CCDS34917.1 CCDS34917.1 Transcript intron_variant - - - - - - rs2954343 8:87236247 T 157724 NM_138817.2 Transcript intron_variant - - - - - - rs7009442 8:87437150 T ENSESTG00000013140 ENSESTT00000033012 Transcript intron_variant - - - - - - rs7009442 8:87437150 T ENSESTG00000013140 ENSESTT00000033032 Transcript intron_variant - - - - - - rs7009442 8:87437150 T ENSESTG00000013140 ENSESTT00000033020 Transcript intron_variant - - - - - - rs7009442 8:87437150 T ENSESTG00000013140 ENSESTT00000033026 Transcript intron_variant - - - - - - rs7009442 8:87437150 T 11059 NM_007013.3 Transcript intron_variant - - - - - - rs7009442 8:87437150 T CCDS6242.1 CCDS6242.1 Transcript intron_variant - - - - - - rs7009442 8:87437150 T ENSESTG00000013140 ENSESTT00000033036 Transcript intron_variant - - - - - - rs7009442 8:87437150 T ENSESTG00000013140 ENSESTT00000033005 Transcript intron_variant - - - - - - rs7009442 8:87437150 T ENSESTG00000013140 ENSESTT00000033030 Transcript intron_variant - - - - - - rs7009442 8:87437150 T ENSESTG00000013140 ENSESTT00000033028 Transcript intron_variant - - - - - - rs7009442 8:87437150 T ENSESTG00000013140 ENSESTT00000033025 Transcript intron_variant - - - - - - rs1372174 8:87665928 G 54714 NM_019098.4 Transcript intron_variant - - - - - - rs1372174 8:87665928 G CCDS6244.1 CCDS6244.1 Transcript intron_variant - - - - - - rs6468467 8:87789890 T - - - intergenic_variant - - - - - - rs10955077 8:87862843 G - - - intergenic_variant - - - - - - rs6468567 8:87952774 G CCDS55259.1 CCDS55259.1 Transcript intron_variant - - - - - - rs6468567 8:87952774 G ENSESTG00000031505 ENSESTT00000079501 Transcript downstream_gene_variant - - - - - - DISTANCE=730 rs6468567 8:87952774 G 168975 NM_173538.2 Transcript intron_variant - - - - - - rs6468614 8:88012397 G CCDS55259.1 CCDS55259.1 Transcript intron_variant - - - - - - rs6468614 8:88012397 G 168975 NM_173538.2 Transcript intron_variant - - - - - - rs7012107 8:88466825 A ENSESTG00000031537 ENSESTT00000079551 Transcript intron_variant - - - - - - rs7012107 8:88466825 A ENSESTG00000031537 ENSESTT00000079528 Transcript intron_variant - - - - - - rs6468950 8:88676263 T - - - intergenic_variant - - - - - - rs2664362 8:89133074 C - ENSR00001442790 RegulatoryFeature regulatory_region_variant - - - - - - rs2664362 8:89133074 C 4325 NM_005941.4 Transcript intron_variant - - - - - - rs2664362 8:89133074 C ENSESTG00000029319 ENSESTT00000073867 Transcript intron_variant - - - - - - rs2664362 8:89133074 C ENSESTG00000029319 ENSESTT00000073889 Transcript intron_variant - - - - - - rs2664362 8:89133074 C CCDS6246.1 CCDS6246.1 Transcript intron_variant - - - - - - rs4961105 8:89903766 G - - - intergenic_variant - - - - - - rs11783913 8:89917049 T - - - intergenic_variant - - - - - - rs4599860 8:90357466 A - - - intergenic_variant - - - - - - rs13282418 8:90424585 T ENSESTG00000022526 ENSESTT00000056868 Transcript downstream_gene_variant - - - - - - DISTANCE=736 rs4961134 8:90429723 A ENSESTG00000022526 ENSESTT00000056868 Transcript upstream_gene_variant - - - - - - DISTANCE=2807 rs6996108 8:90470549 C - - - intergenic_variant - - - - - - rs7465159 8:90496967 C - - - intergenic_variant - - - - - - rs10956106 8:90497941 C - - - intergenic_variant - - - - - - rs147812374 8:90793413 T 8767 NM_003821.5 Transcript intron_variant - - - - - - rs147812374 8:90793413 T CCDS6247.1 CCDS6247.1 Transcript intron_variant - - - - - - rs147812374 8:90793413 T ENSESTG00000016457 ENSESTT00000041449 Transcript downstream_gene_variant - - - - - - DISTANCE=407 rs147812374 8:90793413 T ENSESTG00000016457 ENSESTT00000041427 Transcript intron_variant - - - - - - rs408422 8:91000628 T CCDS6249.1 CCDS6249.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3839 rs408422 8:91000628 T ENSESTG00000016712 ENSESTT00000042005 Transcript upstream_gene_variant - - - - - - DISTANCE=3733 rs408422 8:91000628 T ENSESTG00000016712 ENSESTT00000041927 Transcript intron_variant - - - - - - rs408422 8:91000628 T 4683 NM_002485.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3729 rs448533 8:91000827 C CCDS6249.1 CCDS6249.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4038 rs448533 8:91000827 C ENSESTG00000016712 ENSESTT00000042005 Transcript upstream_gene_variant - - - - - - DISTANCE=3932 rs448533 8:91000827 C ENSESTG00000016712 ENSESTT00000041927 Transcript intron_variant - - - - - - rs448533 8:91000827 C 4683 NM_002485.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3928 rs395719 8:91034115 A ENSESTG00000016571 ENSESTT00000041711 Transcript intron_variant - - - - - - rs395719 8:91034115 A CCDS6250.1 CCDS6250.1 Transcript intron_variant - - - - - - rs395719 8:91034115 A ENSESTG00000016571 ENSESTT00000041746 Transcript intron_variant - - - - - - rs395719 8:91034115 A ENSESTG00000016571 ENSESTT00000041724 Transcript intron_variant - - - - - - rs395719 8:91034115 A ENSESTG00000016571 ENSESTT00000041714 Transcript intron_variant - - - - - - rs395719 8:91034115 A 1666 NM_001359.1 Transcript intron_variant - - - - - - rs408955 8:91034120 T ENSESTG00000016571 ENSESTT00000041711 Transcript intron_variant - - - - - - rs408955 8:91034120 T CCDS6250.1 CCDS6250.1 Transcript intron_variant - - - - - - rs408955 8:91034120 T ENSESTG00000016571 ENSESTT00000041746 Transcript intron_variant - - - - - - rs408955 8:91034120 T ENSESTG00000016571 ENSESTT00000041724 Transcript intron_variant - - - - - - rs408955 8:91034120 T ENSESTG00000016571 ENSESTT00000041714 Transcript intron_variant - - - - - - rs408955 8:91034120 T 1666 NM_001359.1 Transcript intron_variant - - - - - - rs403559 8:91035771 G ENSESTG00000016571 ENSESTT00000041711 Transcript intron_variant - - - - - - rs403559 8:91035771 G CCDS6250.1 CCDS6250.1 Transcript intron_variant - - - - - - rs403559 8:91035771 G ENSESTG00000016571 ENSESTT00000041746 Transcript intron_variant - - - - - - rs403559 8:91035771 G ENSESTG00000016571 ENSESTT00000041724 Transcript intron_variant - - - - - - rs403559 8:91035771 G ENSESTG00000016571 ENSESTT00000041714 Transcript intron_variant - - - - - - rs403559 8:91035771 G 1666 NM_001359.1 Transcript intron_variant - - - - - - rs4734965 8:91418906 G - - - intergenic_variant - - - - - - rs7837385 8:91421115 T - - - intergenic_variant - - - - - - rs7843078 8:91493568 G - - - intergenic_variant - - - - - - rs6994713 8:92332130 T - ENSR00001396129 RegulatoryFeature regulatory_region_variant - - - - - - rs6994713 8:92332130 T CCDS6254.1 CCDS6254.1 Transcript intron_variant - - - - - - rs6994713 8:92332130 T 115111 NM_134266.1 Transcript intron_variant - - - - - - rs6994713 8:92332130 T 115111 NM_052832.2 Transcript intron_variant - - - - - - rs6994713 8:92332130 T CCDS6255.1 CCDS6255.1 Transcript intron_variant - - - - - - rs6994713 8:92332130 T ENSESTG00000004390 ENSESTT00000011112 Transcript intron_variant - - - - - - rs6983382 8:92784258 T - - - intergenic_variant - - - - - - rs2976504 8:92994347 C CCDS6257.1 CCDS6257.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198634.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C CCDS6256.1 CCDS6256.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198633.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198629.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198632.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_004349.3 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198625.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198627.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198631.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198679.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C CCDS56544.1 CCDS56544.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_175635.2 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_175634.2 Transcript intron_variant - - - - - - rs2976504 8:92994347 C CCDS47891.1 CCDS47891.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198628.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_175636.2 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198626.1 Transcript intron_variant - - - - - - rs2976504 8:92994347 C 862 NM_001198630.1 Transcript intron_variant - - - - - - rs7841823 8:93156423 T - - - intergenic_variant - - - - - - rs668971 8:93392635 G - - - intergenic_variant - - - - - - rs686674 8:93455394 T - - - intergenic_variant - - - - - - rs4463397 8:93822137 C - - - intergenic_variant - - - - - - rs183968 8:94038066 A - - - intergenic_variant - - - - - - rs7825390 8:94291818 T ENSESTG00000017771 ENSESTT00000044764 Transcript intron_variant - - - - - - rs7825390 8:94291818 T ENSESTG00000017763 ENSESTT00000044746 Transcript intron_variant - - - - - - rs9297920 8:94302258 A ENSESTG00000017771 ENSESTT00000044764 Transcript intron_variant - - - - - - rs9297920 8:94302258 A ENSESTG00000017763 ENSESTT00000044746 Transcript intron_variant - - - - - - rs1431566 8:94367622 A ENSESTG00000017771 ENSESTT00000044764 Transcript intron_variant - - - - - - rs1431566 8:94367622 A 642924 NR_033858.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4520134 8:94527579 T 642924 NR_033858.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6471392 8:94709812 A CCDS47892.1 CCDS47892.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3064 rs6471392 8:94709812 A ENSESTG00000007365 ENSESTT00000018637 Transcript upstream_gene_variant - - - - - - DISTANCE=2981 rs6471392 8:94709812 A ENSESTG00000007365 ENSESTT00000018615 Transcript upstream_gene_variant - - - - - - DISTANCE=2978 rs6471392 8:94709812 A 137392 NM_145269.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2961 rs6471392 8:94709812 A ENSESTG00000007365 ENSESTT00000018607 Transcript upstream_gene_variant - - - - - - DISTANCE=2966 rs6471392 8:94709812 A ENSESTG00000007365 ENSESTT00000018621 Transcript upstream_gene_variant - - - - - - DISTANCE=2980 rs6471392 8:94709812 A ENSESTG00000007365 ENSESTT00000018599 Transcript upstream_gene_variant - - - - - - DISTANCE=2962 rs6471392 8:94709812 A 642924 NR_033858.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4735245 8:94888826 A ENSESTG00000007487 ENSESTT00000018877 Transcript intron_variant - - - - - - rs3018847 8:95090747 C - - - intergenic_variant - - - - - - rs2514823 8:95230302 G ENSESTG00000007660 ENSESTT00000019382 Transcript upstream_gene_variant - - - - - - DISTANCE=771 rs2514823 8:95230302 G ENSESTG00000007660 ENSESTT00000019376 Transcript upstream_gene_variant - - - - - - DISTANCE=771 rs2514823 8:95230302 G 1015 NM_001144663.1 Transcript upstream_gene_variant - - - - - - DISTANCE=771 rs2448912 8:95252415 T - - - intergenic_variant - - - - - - rs2470719 8:95304111 C - - - intergenic_variant - - - - - - rs2445726 8:95319915 T - - - intergenic_variant - - - - - - rs2515107 8:95418611 G - ENSR00001396504 RegulatoryFeature regulatory_region_variant - - - - - - rs2515107 8:95418611 G ENSESTG00000007603 ENSESTT00000019137 Transcript downstream_gene_variant - - - - - - DISTANCE=4752 rs2515107 8:95418611 G 25788 NM_001205263.1 Transcript intron_variant - - - - - - rs2515107 8:95418611 G ENSESTG00000007603 ENSESTT00000019174 Transcript intron_variant - - - - - - rs2515107 8:95418611 G CCDS6262.1 CCDS6262.1 Transcript intron_variant - - - - - - rs2515107 8:95418611 G 25788 NM_012415.3 Transcript intron_variant - - - - - - rs2515107 8:95418611 G ENSESTG00000007603 ENSESTT00000019185 Transcript intron_variant - - - - - - rs3133660 8:95566574 C - ENSR00001396529 RegulatoryFeature regulatory_region_variant - - - - - - rs3133660 8:95566574 C ENSESTG00000007525 ENSESTT00000018945 Transcript intron_variant - - - - - - rs3133660 8:95566574 C 25962 NM_015496.4 Transcript upstream_gene_variant - - - - - - DISTANCE=828 rs3133660 8:95566574 C 25962 NM_183009.2 Transcript upstream_gene_variant - - - - - - DISTANCE=828 rs3133660 8:95566574 C ENSESTG00000007529 ENSESTT00000018986 Transcript upstream_gene_variant - - - - - - DISTANCE=872 rs3133660 8:95566574 C CCDS47894.1 CCDS47894.1 Transcript upstream_gene_variant - - - - - - DISTANCE=899 rs3133660 8:95566574 C CCDS34923.1 CCDS34923.1 Transcript upstream_gene_variant - - - - - - DISTANCE=899 rs7833809 8:96093055 C - - - intergenic_variant - - - - - - rs1120876 8:96580931 A 100616530 NR_038203.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1120876 8:96580931 A 100616530 NR_038207.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1120876 8:96580931 A 100616530 NR_038205.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1120876 8:96580931 A 100616530 NR_038204.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1120876 8:96580931 A 100616530 NR_038201.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1120876 8:96580931 A 100616530 NR_038206.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1120876 8:96580931 A 100616530 NR_038209.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1120876 8:96580931 A 100616530 NR_038208.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1120876 8:96580931 A 100616530 NR_038202.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134224 8:96609278 C 100616530 NR_038203.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134224 8:96609278 C 100616530 NR_038207.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134224 8:96609278 C 100616530 NR_038205.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134224 8:96609278 C 100616530 NR_038204.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134224 8:96609278 C 100616530 NR_038201.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134224 8:96609278 C 100616530 NR_038206.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134224 8:96609278 C 100616530 NR_038209.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134224 8:96609278 C 100616530 NR_038208.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134224 8:96609278 C 100616530 NR_038202.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1392796 8:96617670 T 100616530 NR_038203.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1392796 8:96617670 T 100616530 NR_038207.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1392796 8:96617670 T 100616530 NR_038205.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1392796 8:96617670 T 100616530 NR_038204.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1392796 8:96617670 T 100616530 NR_038201.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1392796 8:96617670 T 100616530 NR_038206.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1392796 8:96617670 T 100616530 NR_038209.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1392796 8:96617670 T 100616530 NR_038208.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1392796 8:96617670 T 100616530 NR_038202.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134210 8:96626185 A 100616530 NR_038203.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134210 8:96626185 A 100616530 NR_038207.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134210 8:96626185 A 100616530 NR_038205.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134210 8:96626185 A 100616530 NR_038204.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134210 8:96626185 A 100616530 NR_038201.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134210 8:96626185 A 100616530 NR_038206.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134210 8:96626185 A 100616530 NR_038209.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134210 8:96626185 A 100616530 NR_038208.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs3134210 8:96626185 A 100616530 NR_038202.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs261567 8:97020048 C - ENSR00001396780 RegulatoryFeature regulatory_region_variant - - - - - - rs261567 8:97020048 C - - - intergenic_variant - - - - - - rs10283198 8:97104765 C - - - intergenic_variant - - - - - - rs10283199 8:97104796 C - - - intergenic_variant - - - - - - rs13268148 8:97105011 C - - - intergenic_variant - - - - - - rs11782748 8:97332256 C CCDS6271.1 CCDS6271.1 Transcript intron_variant - - - - - - rs11782748 8:97332256 C 9791 NM_014754.1 Transcript intron_variant - - - - - - rs11782748 8:97332256 C ENSESTG00000014572 ENSESTT00000036543 Transcript intron_variant - - - - - - rs2437773 8:97551943 C ENSESTG00000014686 ENSESTT00000036791 Transcript intron_variant - - - - - - rs2437773 8:97551943 C ENSESTG00000014686 ENSESTT00000036801 Transcript downstream_gene_variant - - - - - - DISTANCE=2369 rs2437773 8:97551943 C ENSESTG00000014686 ENSESTT00000036799 Transcript downstream_gene_variant - - - - - - DISTANCE=899 rs2437773 8:97551943 C ENSESTG00000014686 ENSESTT00000036787 Transcript intron_variant - - - - - - rs2437773 8:97551943 C CCDS6272.1 CCDS6272.1 Transcript intron_variant - - - - - - rs2437773 8:97551943 C 6383 NM_002998.3 Transcript intron_variant - - - - - - rs2514766 8:97645496 C - - - intergenic_variant - - - - - - rs6468517 8:97791654 G ENSESTG00000016702 ENSESTT00000042030 Transcript intron_variant - - - - - - rs6468517 8:97791654 G ENSESTG00000016702 ENSESTT00000042014 Transcript intron_variant - - - - - - rs6468517 8:97791654 G 10404 NM_016134.2 Transcript intron_variant - - - - - - rs6468517 8:97791654 G ENSESTG00000016702 ENSESTT00000041982 Transcript intron_variant - - - - - - rs6468517 8:97791654 G ENSESTG00000016702 ENSESTT00000042023 Transcript intron_variant - - - - - - rs6468517 8:97791654 G ENSESTG00000016702 ENSESTT00000041997 Transcript intron_variant - - - - - - rs6468517 8:97791654 G ENSESTG00000016702 ENSESTT00000042028 Transcript intron_variant - - - - - - rs6468517 8:97791654 G ENSESTG00000016702 ENSESTT00000042010 Transcript intron_variant - - - - - - rs6468517 8:97791654 G ENSESTG00000016702 ENSESTT00000042008 Transcript intron_variant - - - - - - rs6468517 8:97791654 G ENSESTG00000016702 ENSESTT00000041995 Transcript intron_variant - - - - - - rs2319930 8:97832919 A ENSESTG00000016702 ENSESTT00000042030 Transcript intron_variant - - - - - - rs2319930 8:97832919 A ENSESTG00000016702 ENSESTT00000042014 Transcript intron_variant - - - - - - rs2319930 8:97832919 A 10404 NM_016134.2 Transcript intron_variant - - - - - - rs2319930 8:97832919 A ENSESTG00000016702 ENSESTT00000041982 Transcript intron_variant - - - - - - rs2319930 8:97832919 A ENSESTG00000016702 ENSESTT00000042023 Transcript intron_variant - - - - - - rs2319930 8:97832919 A ENSESTG00000016702 ENSESTT00000041997 Transcript intron_variant - - - - - - rs2319930 8:97832919 A ENSESTG00000016702 ENSESTT00000042028 Transcript intron_variant - - - - - - rs2319930 8:97832919 A ENSESTG00000016702 ENSESTT00000042010 Transcript intron_variant - - - - - - rs2319930 8:97832919 A ENSESTG00000016702 ENSESTT00000042008 Transcript intron_variant - - - - - - rs2319930 8:97832919 A CCDS6273.1 CCDS6273.1 Transcript intron_variant - - - - - - rs2319930 8:97832919 A ENSESTG00000016702 ENSESTT00000041995 Transcript intron_variant - - - - - - rs7387344 8:97921046 A - ENSR00001443324 RegulatoryFeature regulatory_region_variant - - - - - - rs7387344 8:97921046 A ENSESTG00000016702 ENSESTT00000042030 Transcript intron_variant - - - - - - rs7387344 8:97921046 A ENSESTG00000016702 ENSESTT00000042014 Transcript intron_variant - - - - - - rs7387344 8:97921046 A 10404 NM_016134.2 Transcript intron_variant - - - - - - rs7387344 8:97921046 A ENSESTG00000016702 ENSESTT00000041982 Transcript intron_variant - - - - - - rs7387344 8:97921046 A ENSESTG00000016702 ENSESTT00000042023 Transcript intron_variant - - - - - - rs7387344 8:97921046 A ENSESTG00000016702 ENSESTT00000041997 Transcript intron_variant - - - - - - rs7387344 8:97921046 A ENSESTG00000016702 ENSESTT00000042028 Transcript intron_variant - - - - - - rs7387344 8:97921046 A ENSESTG00000016702 ENSESTT00000042010 Transcript intron_variant - - - - - - rs7387344 8:97921046 A ENSESTG00000016702 ENSESTT00000042008 Transcript intron_variant - - - - - - rs7387344 8:97921046 A CCDS6273.1 CCDS6273.1 Transcript intron_variant - - - - - - rs7387344 8:97921046 A ENSESTG00000016702 ENSESTT00000041995 Transcript intron_variant - - - - - - rs2853258 8:97971647 A - ENSR00001396985 RegulatoryFeature regulatory_region_variant - - - - - - rs2853258 8:97971647 A ENSESTG00000016702 ENSESTT00000042030 Transcript intron_variant - - - - - - rs2853258 8:97971647 A ENSESTG00000016702 ENSESTT00000042014 Transcript intron_variant - - - - - - rs2853258 8:97971647 A 10404 NM_016134.2 Transcript intron_variant - - - - - - rs2853258 8:97971647 A ENSESTG00000016702 ENSESTT00000041982 Transcript intron_variant - - - - - - rs2853258 8:97971647 A ENSESTG00000016702 ENSESTT00000042023 Transcript intron_variant - - - - - - rs2853258 8:97971647 A ENSESTG00000016702 ENSESTT00000041997 Transcript intron_variant - - - - - - rs2853258 8:97971647 A ENSESTG00000016702 ENSESTT00000042028 Transcript intron_variant - - - - - - rs2853258 8:97971647 A ENSESTG00000016702 ENSESTT00000042010 Transcript intron_variant - - - - - - rs2853258 8:97971647 A ENSESTG00000016702 ENSESTT00000042008 Transcript intron_variant - - - - - - rs2853258 8:97971647 A CCDS6273.1 CCDS6273.1 Transcript intron_variant - - - - - - rs2853258 8:97971647 A ENSESTG00000016702 ENSESTT00000041995 Transcript intron_variant - - - - - - rs2513354 8:98094915 C - ENSR00001397003 RegulatoryFeature regulatory_region_variant - - - - - - rs2513354 8:98094915 C ENSESTG00000016702 ENSESTT00000042030 Transcript intron_variant - - - - - - rs2513354 8:98094915 C ENSESTG00000016702 ENSESTT00000042014 Transcript intron_variant - - - - - - rs2513354 8:98094915 C 10404 NM_016134.2 Transcript intron_variant - - - - - - rs2513354 8:98094915 C ENSESTG00000016702 ENSESTT00000041982 Transcript intron_variant - - - - - - rs2513354 8:98094915 C ENSESTG00000016702 ENSESTT00000042023 Transcript intron_variant - - - - - - rs2513354 8:98094915 C ENSESTG00000016702 ENSESTT00000041997 Transcript intron_variant - - - - - - rs2513354 8:98094915 C ENSESTG00000016702 ENSESTT00000042028 Transcript intron_variant - - - - - - rs2513354 8:98094915 C ENSESTG00000016702 ENSESTT00000042010 Transcript intron_variant - - - - - - rs2513354 8:98094915 C ENSESTG00000016702 ENSESTT00000042008 Transcript intron_variant - - - - - - rs2513354 8:98094915 C CCDS6273.1 CCDS6273.1 Transcript intron_variant - - - - - - rs2513354 8:98094915 C ENSESTG00000016702 ENSESTT00000041995 Transcript intron_variant - - - - - - rs2436050 8:98148961 T 10404 NM_016134.2 Transcript intron_variant - - - - - - rs2436050 8:98148961 T ENSESTG00000016702 ENSESTT00000041982 Transcript intron_variant - - - - - - rs2436050 8:98148961 T ENSESTG00000016702 ENSESTT00000042023 Transcript intron_variant - - - - - - rs2436050 8:98148961 T ENSESTG00000016702 ENSESTT00000042028 Transcript intron_variant - - - - - - rs2436050 8:98148961 T ENSESTG00000016702 ENSESTT00000042010 Transcript intron_variant - - - - - - rs2436050 8:98148961 T ENSESTG00000016702 ENSESTT00000042008 Transcript intron_variant - - - - - - rs2436050 8:98148961 T CCDS6273.1 CCDS6273.1 Transcript intron_variant - - - - - - rs2436050 8:98148961 T ENSESTG00000016702 ENSESTT00000041995 Transcript intron_variant - - - - - - rs2451109 8:98201159 C - - - intergenic_variant - - - - - - rs2635163 8:98287622 G ENSESTG00000016755 ENSESTT00000042071 Transcript intron_variant - - - - - - rs2635163 8:98287622 G ENSESTG00000016769 ENSESTT00000042080 Transcript upstream_gene_variant - - - - - - DISTANCE=778 rs2635163 8:98287622 G CCDS34927.1 CCDS34927.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1197 rs2635163 8:98287622 G ENSESTG00000016755 ENSESTT00000042064 Transcript intron_variant - - - - - - rs2635163 8:98287622 G 85453 NM_033512.2 Transcript 3_prime_UTR_variant 2555 - - - - - rs2444867 8:99009662 T ENSESTG00000030817 ENSESTT00000077774 Transcript intron_variant - - - - - - rs2444867 8:99009662 T CCDS55264.1 CCDS55264.1 Transcript intron_variant - - - - - - rs2444867 8:99009662 T ENSESTG00000030817 ENSESTT00000077809 Transcript intron_variant - - - - - - rs2444867 8:99009662 T ENSESTG00000030817 ENSESTT00000077705 Transcript intron_variant - - - - - - rs2444867 8:99009662 T 4147 NM_002380.3 Transcript intron_variant - - - - - - rs2444867 8:99009662 T 4147 NM_030583.2 Transcript intron_variant - - - - - - rs2444867 8:99009662 T ENSESTG00000030817 ENSESTT00000077716 Transcript intron_variant - - - - - - rs2444867 8:99009662 T ENSESTG00000030817 ENSESTT00000077803 Transcript intron_variant - - - - - - rs2444867 8:99009662 T ENSESTG00000030817 ENSESTT00000077783 Transcript intron_variant - - - - - - rs2444867 8:99009662 T CCDS55265.1 CCDS55265.1 Transcript intron_variant - - - - - - rs2447508 8:99140544 A ENSESTG00000031119 ENSESTT00000078690 Transcript intron_variant - - - - - - rs2447508 8:99140544 A ENSESTG00000031119 ENSESTT00000078668 Transcript intron_variant - - - - - - rs2447508 8:99140544 A 10940 NM_001145861.1 Transcript intron_variant - - - - - - rs2447508 8:99140544 A CCDS6277.1 CCDS6277.1 Transcript intron_variant - - - - - - rs2447508 8:99140544 A 10940 NM_001145860.1 Transcript intron_variant - - - - - - rs2447508 8:99140544 A 10940 NM_015029.2 Transcript intron_variant - - - - - - rs2514339 8:99147457 A ENSESTG00000031119 ENSESTT00000078690 Transcript intron_variant - - - - - - rs2514339 8:99147457 A ENSESTG00000031119 ENSESTT00000078668 Transcript intron_variant - - - - - - rs2514339 8:99147457 A 10940 NM_001145861.1 Transcript intron_variant - - - - - - rs2514339 8:99147457 A CCDS6277.1 CCDS6277.1 Transcript intron_variant - - - - - - rs2514339 8:99147457 A 10940 NM_001145860.1 Transcript intron_variant - - - - - - rs2514339 8:99147457 A 10940 NM_015029.2 Transcript intron_variant - - - - - - rs2447490 8:99210249 G ENSESTG00000031427 ENSESTT00000079348 Transcript intron_variant - - - - - - rs2447490 8:99210249 G ENSESTG00000031427 ENSESTT00000079286 Transcript intron_variant - - - - - - rs2447490 8:99210249 G CCDS6278.1 CCDS6278.1 Transcript intron_variant - - - - - - rs2447490 8:99210249 G 79815 NM_024759.1 Transcript intron_variant - - - - - - rs3134311 8:100256993 C CCDS6280.1 CCDS6280.1 Transcript intron_variant - - - - - - rs3134311 8:100256993 C CCDS6281.1 CCDS6281.1 Transcript intron_variant - - - - - - rs3134311 8:100256993 C ENSESTG00000001414 ENSESTT00000003348 Transcript downstream_gene_variant - - - - - - DISTANCE=3607 rs3134311 8:100256993 C ENSESTG00000001414 ENSESTT00000003344 Transcript intron_variant - - - - - - rs3134311 8:100256993 C 157680 NM_152564.4 Transcript intron_variant - - - - - - rs3134311 8:100256993 C 157680 NM_017890.4 Transcript intron_variant - - - - - - rs3134311 8:100256993 C ENSESTG00000001414 ENSESTT00000003351 Transcript downstream_gene_variant - - - - - - DISTANCE=3607 rs1487019 8:100544470 A 693184 NR_030329.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4394 rs1487019 8:100544470 A CCDS6280.1 CCDS6280.1 Transcript intron_variant - - - - - - rs1487019 8:100544470 A CCDS6281.1 CCDS6281.1 Transcript intron_variant - - - - - - rs1487019 8:100544470 A 157680 NM_152564.4 Transcript intron_variant - - - - - - rs1487019 8:100544470 A 157680 NM_017890.4 Transcript intron_variant - - - - - - rs1487019 8:100544470 A 100126309 NR_030596.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4544 rs1788149 8:100759180 T ENSESTG00000006785 ENSESTT00000017253 Transcript intron_variant - - - - - - rs1788149 8:100759180 T CCDS6280.1 CCDS6280.1 Transcript intron_variant - - - - - - rs1788149 8:100759180 T CCDS6281.1 CCDS6281.1 Transcript intron_variant - - - - - - rs1788149 8:100759180 T 157680 NM_152564.4 Transcript intron_variant - - - - - - rs1788149 8:100759180 T 157680 NM_017890.4 Transcript intron_variant - - - - - - rs2446923 8:101160981 G ENSESTG00000006835 ENSESTT00000017397 Transcript upstream_gene_variant - - - - - - DISTANCE=1870 rs2446923 8:101160981 G CCDS6285.1 CCDS6285.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2603 rs2446923 8:101160981 G 286151 NM_001029860.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2882 rs2446923 8:101160981 G 286151 NR_036491.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2882 rs2446923 8:101160981 G ENSESTG00000006835 ENSESTT00000017423 Transcript upstream_gene_variant - - - - - - DISTANCE=1883 rs2446923 8:101160981 G CCDS47904.1 CCDS47904.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3618 rs2446923 8:101160981 G 5440 NM_005034.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1858 rs2453637 8:101160983 C ENSESTG00000006835 ENSESTT00000017397 Transcript upstream_gene_variant - - - - - - DISTANCE=1868 rs2453637 8:101160983 C CCDS6285.1 CCDS6285.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2601 rs2453637 8:101160983 C 286151 NM_001029860.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2884 rs2453637 8:101160983 C 286151 NR_036491.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2884 rs2453637 8:101160983 C ENSESTG00000006835 ENSESTT00000017423 Transcript upstream_gene_variant - - - - - - DISTANCE=1881 rs2453637 8:101160983 C CCDS47904.1 CCDS47904.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3620 rs2453637 8:101160983 C 5440 NM_005034.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1856 rs2453659 8:101200787 A ENSESTG00000006877 ENSESTT00000017477 Transcript upstream_gene_variant - - - - - - DISTANCE=2895 rs2453659 8:101200787 A ENSESTG00000006859 ENSESTT00000017457 Transcript downstream_gene_variant - - - - - - DISTANCE=1411 rs2453659 8:101200787 A CCDS34930.1 CCDS34930.1 Transcript intron_variant - - - - - - rs2453659 8:101200787 A ENSESTG00000006859 ENSESTT00000017464 Transcript downstream_gene_variant - - - - - - DISTANCE=4500 rs2453659 8:101200787 A 6674 NM_172218.2 Transcript intron_variant - - - - - - rs2453659 8:101200787 A 6674 NM_003114.4 Transcript intron_variant - - - - - - rs62532739 8:101223442 G ENSESTG00000006882 ENSESTT00000017488 Transcript upstream_gene_variant - - - - - - DISTANCE=2069 rs62532739 8:101223442 G CCDS34930.1 CCDS34930.1 Transcript intron_variant - - - - - - rs62532739 8:101223442 G 6674 NM_172218.2 Transcript intron_variant - - - - - - rs62532739 8:101223442 G 6674 NM_003114.4 Transcript intron_variant - - - - - - rs1892733 8:101485052 C - ENSR00001397613 RegulatoryFeature regulatory_region_variant - - - - - - rs1892733 8:101485052 C ENSESTG00000006928 ENSESTT00000017586 Transcript upstream_gene_variant - - - - - - DISTANCE=2866 rs1892733 8:101485052 C ENSESTG00000006928 ENSESTT00000017583 Transcript upstream_gene_variant - - - - - - DISTANCE=2851 rs2721977 8:101516850 C ENSESTG00000006928 ENSESTT00000017586 Transcript downstream_gene_variant - - - - - - DISTANCE=3475 rs1892739 8:101538783 C ENSESTG00000006936 ENSESTT00000017635 Transcript downstream_gene_variant - - - - - - DISTANCE=1357 rs1892739 8:101538783 C 157567 NM_001270378.1 Transcript intron_variant - - - - - - rs1892739 8:101538783 C CCDS6287.1 CCDS6287.1 Transcript intron_variant - - - - - - rs1892739 8:101538783 C ENSESTG00000006936 ENSESTT00000017639 Transcript downstream_gene_variant - - - - - - DISTANCE=3013 rs1892739 8:101538783 C 157567 NM_198401.3 Transcript intron_variant - - - - - - rs1892739 8:101538783 C 157567 NM_001270377.1 Transcript intron_variant - - - - - - rs1892739 8:101538783 C CCDS59109.1 CCDS59109.1 Transcript intron_variant - - - - - - rs1892739 8:101538783 C 157567 NM_001270379.1 Transcript intron_variant - - - - - - rs3115888 8:101792500 G - - - intergenic_variant - - - - - - rs10955241 8:101800046 C - - - intergenic_variant - - - - - - rs1264201 8:102230943 A - - - intergenic_variant - - - - - - rs595520 8:102265509 G - - - intergenic_variant - - - - - - rs566789 8:102284750 G - - - intergenic_variant - - - - - - rs2387624 8:102645269 T CCDS34931.1 CCDS34931.1 Transcript intron_variant - - - - - - rs2387624 8:102645269 T ENSESTG00000019675 ENSESTT00000049338 Transcript upstream_gene_variant - - - - - - DISTANCE=3758 rs2387624 8:102645269 T 79977 NM_024915.3 Transcript intron_variant - - - - - - rs3857904 8:103176281 G - - - intergenic_variant - - - - - - rs59015244 8:103220351 G 50484 NM_001172478.1 Transcript 3_prime_UTR_variant 1154 - - - - - rs59015244 8:103220351 G 50484 NM_015713.4 Transcript 3_prime_UTR_variant 1310 - - - - - rs59015244 8:103220351 G CCDS34932.1 CCDS34932.1 Transcript downstream_gene_variant - - - - - - DISTANCE=10 rs59015244 8:103220351 G 50484 NM_001172477.1 Transcript 3_prime_UTR_variant 1291 - - - - - rs59015244 8:103220351 G CCDS55267.1 CCDS55267.1 Transcript downstream_gene_variant - - - - - - DISTANCE=10 rs2511673 8:103626703 C - - - intergenic_variant - - - - - - rs2436871 8:103803014 G - ENSR00001398174 RegulatoryFeature regulatory_region_variant - - - - - - rs2436871 8:103803014 G - - - intergenic_variant - - - - - - rs1447076 8:105192455 T ENSESTG00000006989 ENSESTT00000017734 Transcript intron_variant - - - - - - rs1447076 8:105192455 T CCDS43761.1 CCDS43761.1 Transcript intron_variant - - - - - - rs1447076 8:105192455 T ENSESTG00000006989 ENSESTT00000017736 Transcript intron_variant - - - - - - rs1447076 8:105192455 T 9699 NM_014677.4 Transcript intron_variant - - - - - - rs1447076 8:105192455 T ENSESTG00000006989 ENSESTT00000017730 Transcript intron_variant - - - - - - rs1447076 8:105192455 T CCDS55269.1 CCDS55269.1 Transcript intron_variant - - - - - - rs1447076 8:105192455 T 9699 NM_001100117.2 Transcript intron_variant - - - - - - rs2441803 8:105258043 G ENSESTG00000006989 ENSESTT00000017736 Transcript intron_variant - - - - - - rs2441803 8:105258043 G 9699 NM_014677.4 Transcript intron_variant - - - - - - rs2441803 8:105258043 G ENSESTG00000006989 ENSESTT00000017739 Transcript downstream_gene_variant - - - - - - DISTANCE=804 rs2441803 8:105258043 G CCDS43761.1 CCDS43761.1 Transcript intron_variant - - - - - - rs2441803 8:105258043 G ENSESTG00000006989 ENSESTT00000017734 Transcript intron_variant - - - - - - rs2441803 8:105258043 G CCDS55269.1 CCDS55269.1 Transcript intron_variant - - - - - - rs2441803 8:105258043 G ENSESTG00000006989 ENSESTT00000017730 Transcript intron_variant - - - - - - rs2441803 8:105258043 G 9699 NM_001100117.2 Transcript intron_variant - - - - - - rs2853130 8:105472961 G - ENSR00001398395 RegulatoryFeature regulatory_region_variant - - - - - - rs2853130 8:105472961 G CCDS6302.1 CCDS6302.1 Transcript intron_variant - - - - - - rs2853130 8:105472961 G 1807 NM_001385.2 Transcript intron_variant - - - - - - rs2853130 8:105472961 G ENSESTG00000007035 ENSESTT00000017821 Transcript intron_variant - - - - - - rs4448240 8:105556128 C CCDS6303.1 CCDS6303.1 Transcript intron_variant - - - - - - rs4448240 8:105556128 C ENSESTG00000007022 ENSESTT00000017815 Transcript intron_variant - - - - - - rs4448240 8:105556128 C 29967 NM_013437.4 Transcript intron_variant - - - - - - rs4448240 8:105556128 C ENSESTG00000007022 ENSESTT00000017809 Transcript intron_variant - - - - - - rs4448240 8:105556128 C ENSESTG00000007022 ENSESTT00000017804 Transcript intron_variant - - - - - - rs4448240 8:105556128 C CCDS47907.1 CCDS47907.1 Transcript intron_variant - - - - - - rs4448240 8:105556128 C 29967 NM_001135703.2 Transcript intron_variant - - - - - - rs2959029 8:105618418 T - ENSR00001443902 RegulatoryFeature regulatory_region_variant - - - - - - rs2959029 8:105618418 T - - - intergenic_variant - - - - - - rs4439091 8:105687781 C - - - intergenic_variant - - - - - - rs7840835 8:106241387 A - - - intergenic_variant - - - - - - rs3098806 8:106786177 A ENSESTG00000000037 ENSESTT00000000111 Transcript intron_variant - - - - - - rs3098806 8:106786177 A ENSESTG00000000037 ENSESTT00000000108 Transcript intron_variant - - - - - - rs3098806 8:106786177 A ENSESTG00000025520 ENSESTT00000064385 Transcript intron_variant - - - - - - rs3098806 8:106786177 A CCDS47908.1 CCDS47908.1 Transcript intron_variant - - - - - - rs3098806 8:106786177 A 23414 NM_012082.3 Transcript intron_variant - - - - - - rs3098806 8:106786177 A ENSESTG00000025520 ENSESTT00000064380 Transcript intron_variant - - - - - - rs9642801 8:106891438 T - - - intergenic_variant - - - - - - rs4307313 8:107383006 G 55074 NM_001198533.1 Transcript intron_variant - - - - - - rs4307313 8:107383006 G CCDS56547.1 CCDS56547.1 Transcript intron_variant - - - - - - rs4307313 8:107383006 G CCDS47909.1 CCDS47909.1 Transcript intron_variant - - - - - - rs4307313 8:107383006 G 55074 NM_018002.3 Transcript intron_variant - - - - - - rs1789966 8:107474421 A 55074 NM_001198533.1 Transcript intron_variant - - - - - - rs1789966 8:107474421 A CCDS47909.1 CCDS47909.1 Transcript intron_variant - - - - - - rs1789966 8:107474421 A ENSESTG00000000048 ENSESTT00000000138 Transcript intron_variant - - - - - - rs1789966 8:107474421 A CCDS56547.1 CCDS56547.1 Transcript intron_variant - - - - - - rs1789966 8:107474421 A ENSESTG00000000048 ENSESTT00000000135 Transcript intron_variant - - - - - - rs1789966 8:107474421 A 55074 NM_001198532.1 Transcript intron_variant - - - - - - rs1789966 8:107474421 A CCDS56548.1 CCDS56548.1 Transcript intron_variant - - - - - - rs1789966 8:107474421 A 55074 NM_018002.3 Transcript intron_variant - - - - - - rs2444316 8:107476257 A 55074 NM_001198533.1 Transcript intron_variant - - - - - - rs2444316 8:107476257 A CCDS47909.1 CCDS47909.1 Transcript intron_variant - - - - - - rs2444316 8:107476257 A ENSESTG00000000048 ENSESTT00000000138 Transcript intron_variant - - - - - - rs2444316 8:107476257 A CCDS56547.1 CCDS56547.1 Transcript intron_variant - - - - - - rs2444316 8:107476257 A ENSESTG00000000048 ENSESTT00000000135 Transcript intron_variant - - - - - - rs2444316 8:107476257 A 55074 NM_001198532.1 Transcript intron_variant - - - - - - rs2444316 8:107476257 A CCDS56548.1 CCDS56548.1 Transcript intron_variant - - - - - - rs2444316 8:107476257 A 55074 NM_018002.3 Transcript intron_variant - - - - - - rs1283700 8:108438699 G ENSESTG00000002121 ENSESTT00000005224 Transcript intron_variant - - - - - - rs1283700 8:108438699 G 284 NM_001146.3 Transcript intron_variant - - - - - - rs1283700 8:108438699 G CCDS6306.1 CCDS6306.1 Transcript intron_variant - - - - - - rs1283700 8:108438699 G ENSESTG00000002121 ENSESTT00000005220 Transcript intron_variant - - - - - - rs1283700 8:108438699 G 284 NM_001199859.1 Transcript intron_variant - - - - - - rs1283700 8:108438699 G CCDS56551.1 CCDS56551.1 Transcript intron_variant - - - - - - rs281680 8:108574047 T - - - intergenic_variant - - - - - - rs2514847 8:109083203 C ENSESTG00000022340 ENSESTT00000056438 Transcript intron_variant - - - - - - rs2514847 8:109083203 C 340419 NM_178565.4 Transcript intron_variant - - - - - - rs2514847 8:109083203 C ENSESTG00000022340 ENSESTT00000056378 Transcript intron_variant - - - - - - rs2514847 8:109083203 C CCDS6307.1 CCDS6307.1 Transcript intron_variant - - - - - - rs2514847 8:109083203 C ENSESTG00000022340 ENSESTT00000056415 Transcript intron_variant - - - - - - rs2514847 8:109083203 C ENSESTG00000022340 ENSESTT00000056367 Transcript intron_variant - - - - - - rs669485 8:109163564 C - - - intergenic_variant - - - - - - rs2935789 8:109739271 G - - - intergenic_variant - - - - - - rs13269504 8:109892055 G - - - intergenic_variant - - - - - - rs4469427 8:109892244 A - - - intergenic_variant - - - - - - rs973168 8:110449535 A 93035 NM_177531.4 Transcript intron_variant - - - - - - rs973168 8:110449535 A CCDS47911.1 CCDS47911.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A ENSESTG00000022564 ENSESTT00000057131 Transcript intron_variant - - - - - - rs2844237 8:110610789 A ENSESTG00000022564 ENSESTT00000057040 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099750.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099756.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099745.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099747.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A ENSESTG00000022564 ENSESTT00000057060 Transcript intron_variant - - - - - - rs2844237 8:110610789 A CCDS43763.1 CCDS43763.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A CCDS47912.1 CCDS47912.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099748.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A ENSESTG00000022564 ENSESTT00000057010 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099744.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099743.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A CCDS43764.1 CCDS43764.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099753.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099746.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A CCDS55271.1 CCDS55271.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099755.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099752.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099754.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_017786.5 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099751.1 Transcript intron_variant - - - - - - rs2844237 8:110610789 A 55638 NM_001099749.1 Transcript intron_variant - - - - - - rs1017877 8:110780032 A - - - intergenic_variant - - - - - - rs7827933 8:111005116 C - - - intergenic_variant - - - - - - rs1949759 8:111327051 A - - - intergenic_variant - - - - - - rs1389672 8:111625243 T - - - intergenic_variant - - - - - - rs10098789 8:111743006 C - - - intergenic_variant - - - - - - rs4371980 8:111768775 A - - - intergenic_variant - - - - - - rs4573248 8:111781957 A - - - intergenic_variant - - - - - - rs6415453 8:111818214 T - - - intergenic_variant - - - - - - rs4554441 8:111818282 T - - - intergenic_variant - - - - - - rs2882625 8:111923684 T - - - intergenic_variant - - - - - - rs7460671 8:111961299 T - - - intergenic_variant - - - - - - rs13279593 8:112394633 C - - - intergenic_variant - - - - - - rs2882778 8:112421023 A - - - intergenic_variant - - - - - - rs1346653 8:112450511 G - - - intergenic_variant - - - - - - rs2564407 8:112533324 T - - - intergenic_variant - - - - - - rs7011971 8:112700947 G - - - intergenic_variant - - - - - - rs9297462 8:113054956 G - - - intergenic_variant - - - - - - rs918151 8:113318612 T ENSESTG00000002257 ENSESTT00000005628 Transcript upstream_gene_variant - - - - - - DISTANCE=1585 rs918151 8:113318612 T CCDS6316.2 CCDS6316.2 Transcript intron_variant - - - - - - rs918151 8:113318612 T 114788 NM_198124.1 Transcript intron_variant - - - - - - rs918151 8:113318612 T 114788 NM_052900.2 Transcript intron_variant - - - - - - rs918151 8:113318612 T CCDS6317.1 CCDS6317.1 Transcript intron_variant - - - - - - rs918151 8:113318612 T 114788 NM_198123.1 Transcript intron_variant - - - - - - rs918151 8:113318612 T CCDS6315.1 CCDS6315.1 Transcript intron_variant - - - - - - rs1377369 8:113528838 G ENSESTG00000017789 ENSESTT00000044786 Transcript intron_variant - - - - - - rs1377369 8:113528838 G CCDS6316.2 CCDS6316.2 Transcript intron_variant - - - - - - rs1377369 8:113528838 G 114788 NM_198124.1 Transcript intron_variant - - - - - - rs1377369 8:113528838 G 114788 NM_052900.2 Transcript intron_variant - - - - - - rs1377369 8:113528838 G CCDS6317.1 CCDS6317.1 Transcript intron_variant - - - - - - rs1377369 8:113528838 G 114788 NM_198123.1 Transcript intron_variant - - - - - - rs1377369 8:113528838 G CCDS6315.1 CCDS6315.1 Transcript intron_variant - - - - - - rs12155659 8:113614929 T CCDS6316.2 CCDS6316.2 Transcript intron_variant - - - - - - rs12155659 8:113614929 T 114788 NM_198124.1 Transcript intron_variant - - - - - - rs12155659 8:113614929 T 114788 NM_052900.2 Transcript intron_variant - - - - - - rs12155659 8:113614929 T CCDS6317.1 CCDS6317.1 Transcript intron_variant - - - - - - rs12155659 8:113614929 T 114788 NM_198123.1 Transcript intron_variant - - - - - - rs12155659 8:113614929 T CCDS6315.1 CCDS6315.1 Transcript intron_variant - - - - - - rs28661463 8:114401027 T ENSESTG00000017712 ENSESTT00000044651 Transcript intron_variant - - - - - - rs28661463 8:114401027 T ENSESTG00000017712 ENSESTT00000044683 Transcript intron_variant - - - - - - rs28661463 8:114401027 T 114788 NM_198123.1 Transcript intron_variant - - - - - - rs28661463 8:114401027 T CCDS6316.2 CCDS6316.2 Transcript intron_variant - - - - - - rs28661463 8:114401027 T 114788 NM_052900.2 Transcript intron_variant - - - - - - rs28661463 8:114401027 T ENSESTG00000017712 ENSESTT00000044661 Transcript intron_variant - - - - - - rs28661463 8:114401027 T ENSESTG00000017712 ENSESTT00000044671 Transcript intron_variant - - - - - - rs28661463 8:114401027 T CCDS6315.1 CCDS6315.1 Transcript intron_variant - - - - - - rs2458065 8:114958378 T - - - intergenic_variant - - - - - - rs7460238 8:115358067 A - - - intergenic_variant - - - - - - rs2575950 8:116076794 C - - - intergenic_variant - - - - - - rs800873 8:116411898 C - - - intergenic_variant - - - - - - rs231153 8:116421434 C CCDS6318.2 CCDS6318.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4817 rs231153 8:116421434 C 7227 NM_014112.2 Transcript 3_prime_UTR_variant 9280 - - - - - rs800898 8:116423424 C CCDS6318.2 CCDS6318.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2827 rs800898 8:116423424 C ENSESTG00000022731 ENSESTT00000057371 Transcript downstream_gene_variant - - - - - - DISTANCE=3194 rs800898 8:116423424 C 7227 NM_014112.2 Transcript 3_prime_UTR_variant 7290 - - - - - rs1735504 8:116423490 T CCDS6318.2 CCDS6318.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2761 rs1735504 8:116423490 T ENSESTG00000022731 ENSESTT00000057371 Transcript downstream_gene_variant - - - - - - DISTANCE=3128 rs1735504 8:116423490 T 7227 NM_014112.2 Transcript 3_prime_UTR_variant 7224 - - - - - rs1180629 8:116431476 A - ENSR00001444280 RegulatoryFeature regulatory_region_variant - - - - - - rs1180629 8:116431476 A CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs1180629 8:116431476 A ENSESTG00000022731 ENSESTT00000057371 Transcript intron_variant - - - - - - rs1180629 8:116431476 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs800894 8:116436480 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs800894 8:116436480 T ENSESTG00000022731 ENSESTT00000057371 Transcript intron_variant - - - - - - rs800894 8:116436480 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs800893 8:116436543 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs800893 8:116436543 T ENSESTG00000022731 ENSESTT00000057371 Transcript intron_variant - - - - - - rs800893 8:116436543 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs1180632 8:116444438 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs1180632 8:116444438 T ENSESTG00000022731 ENSESTT00000057371 Transcript intron_variant - - - - - - rs1180632 8:116444438 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs1180639 8:116444613 G CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs1180639 8:116444613 G ENSESTG00000022731 ENSESTT00000057371 Transcript intron_variant - - - - - - rs1180639 8:116444613 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs1180641 8:116444664 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs1180641 8:116444664 C ENSESTG00000022731 ENSESTT00000057371 Transcript intron_variant - - - - - - rs1180641 8:116444664 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs1180643 8:116444718 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs1180643 8:116444718 T ENSESTG00000022731 ENSESTT00000057371 Transcript intron_variant - - - - - - rs1180643 8:116444718 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs760367 8:116445445 A CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs760367 8:116445445 A ENSESTG00000022731 ENSESTT00000057371 Transcript intron_variant - - - - - - rs760367 8:116445445 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs145893057 8:116514414 A - ENSR00001399401 RegulatoryFeature regulatory_region_variant - - - - - - rs145893057 8:116514414 A CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs145893057 8:116514414 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs800876 8:116523653 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs800876 8:116523653 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs800875 8:116523716 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs800875 8:116523716 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs140909587 8:116526132 A CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs140909587 8:116526132 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2625681 8:116531930 G CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2625681 8:116531930 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2625680 8:116532101 G CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2625680 8:116532101 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2625679 8:116532264 G CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2625679 8:116532264 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2625677 8:116533273 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2625677 8:116533273 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2625676 8:116533275 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2625676 8:116533275 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737201 8:116533364 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2737201 8:116533364 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737202 8:116533589 A CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2737202 8:116533589 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs800919 8:116537291 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs800919 8:116537291 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs146216041 8:116538714 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs146216041 8:116538714 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs800917 8:116538748 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs800917 8:116538748 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs800916 8:116539949 G CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs800916 8:116539949 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs6469598 8:116573654 G CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs6469598 8:116573654 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs6469598 8:116573654 G ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs6469599 8:116573735 G CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs6469599 8:116573735 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs6469599 8:116573735 G ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs4876606 8:116589403 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs4876606 8:116589403 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs4876606 8:116589403 T ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs4876343 8:116589607 A CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs4876343 8:116589607 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs4876343 8:116589607 A ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs2721968 8:116604838 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2721968 8:116604838 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2721968 8:116604838 T ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs2721969 8:116604996 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2721969 8:116604996 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2721969 8:116604996 C ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs2737204 8:116605063 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2737204 8:116605063 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737204 8:116605063 C ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs2721927 8:116608521 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2721927 8:116608521 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2721927 8:116608521 T ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs2737208 8:116614610 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2737208 8:116614610 C ENSESTG00000025207 ENSESTT00000063726 Transcript downstream_gene_variant - - - - - - DISTANCE=2597 rs2737208 8:116614610 C ENSESTG00000025207 ENSESTT00000063695 Transcript downstream_gene_variant - - - - - - DISTANCE=2597 rs2737208 8:116614610 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737208 8:116614610 C ENSESTG00000025207 ENSESTT00000063718 Transcript downstream_gene_variant - - - - - - DISTANCE=2597 rs2737208 8:116614610 C ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs2737209 8:116614761 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2737209 8:116614761 C ENSESTG00000025207 ENSESTT00000063726 Transcript downstream_gene_variant - - - - - - DISTANCE=2446 rs2737209 8:116614761 C ENSESTG00000025207 ENSESTT00000063695 Transcript downstream_gene_variant - - - - - - DISTANCE=2446 rs2737209 8:116614761 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737209 8:116614761 C ENSESTG00000025207 ENSESTT00000063718 Transcript downstream_gene_variant - - - - - - DISTANCE=2446 rs2737209 8:116614761 C ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs2737210 8:116614813 A CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2737210 8:116614813 A ENSESTG00000025207 ENSESTT00000063726 Transcript downstream_gene_variant - - - - - - DISTANCE=2394 rs2737210 8:116614813 A ENSESTG00000025207 ENSESTT00000063695 Transcript downstream_gene_variant - - - - - - DISTANCE=2394 rs2737210 8:116614813 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737210 8:116614813 A ENSESTG00000025207 ENSESTT00000063718 Transcript downstream_gene_variant - - - - - - DISTANCE=2394 rs2737210 8:116614813 A ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs2737211 8:116614954 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2737211 8:116614954 T ENSESTG00000025207 ENSESTT00000063726 Transcript downstream_gene_variant - - - - - - DISTANCE=2253 rs2737211 8:116614954 T ENSESTG00000025207 ENSESTT00000063695 Transcript downstream_gene_variant - - - - - - DISTANCE=2253 rs2737211 8:116614954 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737211 8:116614954 T ENSESTG00000025207 ENSESTT00000063718 Transcript downstream_gene_variant - - - - - - DISTANCE=2253 rs2737211 8:116614954 T ENSESTG00000025273 ENSESTT00000063766 Transcript intron_variant - - - - - - rs2976473 8:116623399 A CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2976473 8:116623399 A ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2976473 8:116623399 A ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2976473 8:116623399 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2976473 8:116623399 A ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2721935 8:116629162 T CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs2721935 8:116629162 T ENSESTG00000025207 ENSESTT00000063629 Transcript downstream_gene_variant - - - - - - DISTANCE=2978 rs2721935 8:116629162 T ENSESTG00000025207 ENSESTT00000063649 Transcript downstream_gene_variant - - - - - - DISTANCE=2839 rs2721935 8:116629162 T ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2721935 8:116629162 T ENSESTG00000025207 ENSESTT00000063669 Transcript downstream_gene_variant - - - - - - DISTANCE=2906 rs2721935 8:116629162 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2721935 8:116629162 T ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2721935 8:116629162 T ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs146322404 8:116629202 C CCDS6318.2 CCDS6318.2 Transcript intron_variant - - - - - - rs146322404 8:116629202 C ENSESTG00000025207 ENSESTT00000063629 Transcript downstream_gene_variant - - - - - - DISTANCE=2938 rs146322404 8:116629202 C ENSESTG00000025207 ENSESTT00000063649 Transcript downstream_gene_variant - - - - - - DISTANCE=2799 rs146322404 8:116629202 C ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs146322404 8:116629202 C ENSESTG00000025207 ENSESTT00000063669 Transcript downstream_gene_variant - - - - - - DISTANCE=2866 rs146322404 8:116629202 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs146322404 8:116629202 C ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs146322404 8:116629202 C ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2721947 8:116642594 A ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2721947 8:116642594 A ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2721947 8:116642594 A ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2721947 8:116642594 A ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2721947 8:116642594 A ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2721947 8:116642594 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2721947 8:116642594 A ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2721947 8:116642594 A ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2721949 8:116643740 A ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2721949 8:116643740 A ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2721949 8:116643740 A ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2721949 8:116643740 A ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2721949 8:116643740 A ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2721949 8:116643740 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2721949 8:116643740 A ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2721949 8:116643740 A ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs1997584 8:116645532 A ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs1997584 8:116645532 A ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs1997584 8:116645532 A ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs1997584 8:116645532 A ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs1997584 8:116645532 A ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs1997584 8:116645532 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs1997584 8:116645532 A ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs1997584 8:116645532 A ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs10093757 8:116648628 G ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs10093757 8:116648628 G ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs10093757 8:116648628 G ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs10093757 8:116648628 G ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs10093757 8:116648628 G ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs10093757 8:116648628 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs10093757 8:116648628 G ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs10093757 8:116648628 G ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs1983542 8:116654687 T ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs1983542 8:116654687 T ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs1983542 8:116654687 T ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs1983542 8:116654687 T ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs1983542 8:116654687 T ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs1983542 8:116654687 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs1983542 8:116654687 T ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs1983542 8:116654687 T ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs141427039 8:116660394 G - ENSR00001399416 RegulatoryFeature regulatory_region_variant - - - - - - rs141427039 8:116660394 G ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs141427039 8:116660394 G ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs141427039 8:116660394 G ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs141427039 8:116660394 G ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs141427039 8:116660394 G ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs141427039 8:116660394 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs141427039 8:116660394 G ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs141427039 8:116660394 G ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2049871 8:116661715 G ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2049871 8:116661715 G ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2049871 8:116661715 G ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2049871 8:116661715 G ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2049871 8:116661715 G ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2049871 8:116661715 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2049871 8:116661715 G ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2049871 8:116661715 G ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2721964 8:116661814 G ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2721964 8:116661814 G ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2721964 8:116661814 G ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2721964 8:116661814 G ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2721964 8:116661814 G ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2721964 8:116661814 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2721964 8:116661814 G ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2721964 8:116661814 G ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs725715 8:116664166 A ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs725715 8:116664166 A ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs725715 8:116664166 A ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs725715 8:116664166 A ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs725715 8:116664166 A ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs725715 8:116664166 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs725715 8:116664166 A ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs725715 8:116664166 A ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2737256 8:116665733 T ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2737256 8:116665733 T ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2737256 8:116665733 T ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2737256 8:116665733 T ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2737256 8:116665733 T ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2737256 8:116665733 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737256 8:116665733 T ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2737256 8:116665733 T ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2737258 8:116665944 G ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2737258 8:116665944 G ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2737258 8:116665944 G ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2737258 8:116665944 G ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2737258 8:116665944 G ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2737258 8:116665944 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737258 8:116665944 G ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2737258 8:116665944 G ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2721967 8:116666348 T ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2721967 8:116666348 T ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2721967 8:116666348 T ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2721967 8:116666348 T ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2721967 8:116666348 T ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2721967 8:116666348 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2721967 8:116666348 T ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2721967 8:116666348 T ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs150325866 8:116666417 T ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs150325866 8:116666417 T ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs150325866 8:116666417 T ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs150325866 8:116666417 T ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs150325866 8:116666417 T ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs150325866 8:116666417 T 7227 NM_014112.2 Transcript intron_variant - - - - - - rs150325866 8:116666417 T ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs150325866 8:116666417 T ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs144923076 8:116666449 A ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs144923076 8:116666449 A ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs144923076 8:116666449 A ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs144923076 8:116666449 A ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs144923076 8:116666449 A ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs144923076 8:116666449 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs144923076 8:116666449 A ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs144923076 8:116666449 A ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2737260 8:116667211 G ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2737260 8:116667211 G ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2737260 8:116667211 G ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2737260 8:116667211 G ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2737260 8:116667211 G ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2737260 8:116667211 G 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737260 8:116667211 G ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2737260 8:116667211 G ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2737262 8:116667305 A ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2737262 8:116667305 A ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2737262 8:116667305 A ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2737262 8:116667305 A ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2737262 8:116667305 A ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2737262 8:116667305 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2737262 8:116667305 A ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2737262 8:116667305 A ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs142535292 8:116671781 C ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs142535292 8:116671781 C ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs142535292 8:116671781 C ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs142535292 8:116671781 C ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs142535292 8:116671781 C ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs142535292 8:116671781 C 7227 NM_014112.2 Transcript intron_variant - - - - - - rs142535292 8:116671781 C ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs142535292 8:116671781 C ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2721970 8:116671835 A ENSESTG00000025207 ENSESTT00000063705 Transcript intron_variant - - - - - - rs2721970 8:116671835 A ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2721970 8:116671835 A ENSESTG00000025207 ENSESTT00000063649 Transcript intron_variant - - - - - - rs2721970 8:116671835 A ENSESTG00000025207 ENSESTT00000063718 Transcript intron_variant - - - - - - rs2721970 8:116671835 A ENSESTG00000025207 ENSESTT00000063669 Transcript intron_variant - - - - - - rs2721970 8:116671835 A 7227 NM_014112.2 Transcript intron_variant - - - - - - rs2721970 8:116671835 A ENSESTG00000025207 ENSESTT00000063695 Transcript intron_variant - - - - - - rs2721970 8:116671835 A ENSESTG00000025207 ENSESTT00000063726 Transcript intron_variant - - - - - - rs2737267 8:116682323 T ENSESTG00000025207 ENSESTT00000063705 Transcript upstream_gene_variant - - - - - - DISTANCE=1802 rs2737267 8:116682323 T ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2737267 8:116682323 T ENSESTG00000025207 ENSESTT00000063695 Transcript upstream_gene_variant - - - - - - DISTANCE=1418 rs2737267 8:116682323 T 7227 NM_014112.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1095 rs2737267 8:116682323 T ENSESTG00000025207 ENSESTT00000063649 Transcript upstream_gene_variant - - - - - - DISTANCE=613 rs2737267 8:116682323 T ENSESTG00000025207 ENSESTT00000063718 Transcript upstream_gene_variant - - - - - - DISTANCE=2084 rs2737267 8:116682323 T ENSESTG00000025207 ENSESTT00000063669 Transcript upstream_gene_variant - - - - - - DISTANCE=1193 rs800573 8:116718319 C ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs146426808 8:116726894 T ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2694026 8:116726974 T ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs5001447 8:116748300 A ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2262126 8:116793283 C ENSESTG00000025207 ENSESTT00000063629 Transcript intron_variant - - - - - - rs2736210 8:116826515 C ENSESTG00000025207 ENSESTT00000063629 Transcript upstream_gene_variant - - - - - - DISTANCE=4616 rs7827728 8:116952874 G - - - intergenic_variant - - - - - - rs1012865 8:116971987 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2873126 8:117177634 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs61722764 8:117188344 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2316317 8:117205459 T 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs148250747 8:117226952 T 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs799866 8:117238349 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1569340 8:117246709 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs799893 8:117247927 T 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs698743 8:117253145 C 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs799863 8:117263138 G 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs698745 8:117275032 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs698746 8:117275048 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs799853 8:117275065 G 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs799896 8:117276127 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs146373165 8:117291379 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs139678905 8:117291397 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4876350 8:117307151 A 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7001070 8:117307704 G 100859921 NR_046215.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10092515 8:117610508 G - - - intergenic_variant - - - - - - rs4415350 8:117627682 C - - - intergenic_variant - - - - - - rs1446533 8:117966109 G 169026 NM_001172813.1 Transcript intron_variant - - - - - - rs1446533 8:117966109 G ENSESTG00000007103 ENSESTT00000017963 Transcript intron_variant - - - - - - rs1446533 8:117966109 G 169026 NM_001172815.1 Transcript intron_variant - - - - - - rs1446533 8:117966109 G 169026 NM_001172811.1 Transcript intron_variant - - - - - - rs2464590 8:118191538 G 169026 NM_173851.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2585 rs2464590 8:118191538 G 169026 NM_001172813.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2585 rs2464590 8:118191538 G 169026 NM_001172815.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2585 rs2464590 8:118191538 G 169026 NM_001172814.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2585 rs2464590 8:118191538 G 169026 NM_001172811.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2585 rs1155714 8:118456466 G - - - intergenic_variant - - - - - - rs4876382 8:118674895 C - - - intergenic_variant - - - - - - rs218025 8:118724002 G - - - intergenic_variant - - - - - - rs218027 8:118724862 G - ENSR00001444474 RegulatoryFeature regulatory_region_variant - - - - - - rs218027 8:118724862 G - - - intergenic_variant - - - - - - rs218028 8:118725318 G - ENSR00001399654 RegulatoryFeature regulatory_region_variant - - - - - - rs218028 8:118725318 G - - - intergenic_variant - - - - - - rs218031 8:118732441 T - - - intergenic_variant - - - - - - rs3115766 8:118754763 G - - - intergenic_variant - - - - - - rs3115765 8:118754768 G - - - intergenic_variant - - - - - - rs2940432 8:118754815 G - - - intergenic_variant - - - - - - rs12676223 8:118759718 C - - - intergenic_variant - - - - - - rs218015 8:118763523 G - - - intergenic_variant - - - - - - rs2460961 8:119598047 T ENSESTG00000010578 ENSESTT00000026473 Transcript intron_variant - - - - - - rs2460961 8:119598047 T ENSESTG00000010578 ENSESTT00000026468 Transcript intron_variant - - - - - - rs2460961 8:119598047 T 401474 NM_001101676.1 Transcript intron_variant - - - - - - rs2460961 8:119598047 T CCDS6325.1 CCDS6325.1 Transcript intron_variant - - - - - - rs2460961 8:119598047 T ENSESTG00000010578 ENSESTT00000026464 Transcript intron_variant - - - - - - rs2460961 8:119598047 T CCDS47913.1 CCDS47913.1 Transcript intron_variant - - - - - - rs2460961 8:119598047 T 401474 NM_207506.2 Transcript intron_variant - - - - - - rs3133591 8:119766948 G - - - intergenic_variant - - - - - - rs4385489 8:119968342 G - ENSR00001399923 RegulatoryFeature regulatory_region_variant - - - - - - rs4385489 8:119968342 G ENSESTG00000003896 ENSESTT00000009851 Transcript upstream_gene_variant - - - - - - DISTANCE=3966 rs4385489 8:119968342 G CCDS6326.1 CCDS6326.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4282 rs4385489 8:119968342 G 4982 NM_002546.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3959 rs4385489 8:119968342 G ENSESTG00000003896 ENSESTT00000009848 Transcript upstream_gene_variant - - - - - - DISTANCE=3966 rs2169381 8:120389379 C - - - intergenic_variant - - - - - - rs1017396 8:120698068 C ENSESTG00000035084 ENSESTT00000088659 Transcript intron_variant - - - - - - rs10108536 8:120841733 G 79075 NM_024094.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4448 rs10108536 8:120841733 G ENSESTG00000035064 ENSESTT00000088622 Transcript intron_variant - - - - - - rs10108536 8:120841733 G ENSESTG00000035064 ENSESTT00000088619 Transcript intron_variant - - - - - - rs10108536 8:120841733 G CCDS34937.1 CCDS34937.1 Transcript intron_variant - - - - - - rs10108536 8:120841733 G 6873 NM_003184.3 Transcript intron_variant - - - - - - rs1158849 8:121305984 T ENSESTG00000035004 ENSESTT00000088525 Transcript upstream_gene_variant - - - - - - DISTANCE=3758 rs1158849 8:121305984 T ENSESTG00000035004 ENSESTT00000088521 Transcript intron_variant - - - - - - rs1158849 8:121305984 T CCDS34938.1 CCDS34938.1 Transcript intron_variant - - - - - - rs1158849 8:121305984 T ENSESTG00000035004 ENSESTT00000088510 Transcript intron_variant - - - - - - rs1158849 8:121305984 T ENSESTG00000035004 ENSESTT00000088513 Transcript intron_variant - - - - - - rs1158849 8:121305984 T 7373 NM_021110.1 Transcript intron_variant - - - - - - rs1158849 8:121305984 T ENSESTG00000035004 ENSESTT00000088507 Transcript intron_variant - - - - - - rs2054149 8:121351132 T ENSESTG00000035004 ENSESTT00000088525 Transcript intron_variant - - - - - - rs2054149 8:121351132 T ENSESTG00000035004 ENSESTT00000088530 Transcript intron_variant - - - - - - rs2054149 8:121351132 T ENSESTG00000035004 ENSESTT00000088521 Transcript intron_variant - - - - - - rs2054149 8:121351132 T CCDS34938.1 CCDS34938.1 Transcript intron_variant - - - - - - rs2054149 8:121351132 T 7373 NM_021110.1 Transcript intron_variant - - - - - - rs11786108 8:121527660 C ENSESTG00000028048 ENSESTT00000070580 Transcript upstream_gene_variant - - - - - - DISTANCE=2626 rs11786108 8:121527660 C 27085 NM_022045.3 Transcript intron_variant - - - - - - rs11786108 8:121527660 C ENSESTG00000028014 ENSESTT00000070541 Transcript intron_variant - - - - - - rs11786108 8:121527660 C CCDS6333.1 CCDS6333.1 Transcript intron_variant - - - - - - rs2916162 8:122092233 G - - - intergenic_variant - - - - - - rs2656121 8:122233922 C - - - intergenic_variant - - - - - - rs1605946 8:123129073 C - - - intergenic_variant - - - - - - rs7828182 8:123366188 T - - - intergenic_variant - - - - - - rs12540999 8:123486565 C - ENSR00001400401 RegulatoryFeature regulatory_region_variant - - - - - - rs12540999 8:123486565 C - - - intergenic_variant - - - - - - rs2948637 8:123568779 A - - - intergenic_variant - - - - - - rs2948634 8:123598561 T - - - intergenic_variant - - - - - - rs4870813 8:123797611 T ENSESTG00000022379 ENSESTT00000056549 Transcript intron_variant - - - - - - rs4870813 8:123797611 T 22882 NM_014943.3 Transcript intron_variant - - - - - - rs4870813 8:123797611 T ENSESTG00000022379 ENSESTT00000056514 Transcript intron_variant - - - - - - rs4870817 8:123846445 C ENSESTG00000022379 ENSESTT00000056549 Transcript intron_variant - - - - - - rs4870817 8:123846445 C 22882 NM_014943.3 Transcript intron_variant - - - - - - rs4870817 8:123846445 C ENSESTG00000022379 ENSESTT00000056514 Transcript intron_variant - - - - - - rs2891671 8:124051947 A CCDS6337.1 CCDS6337.1 Transcript intron_variant - - - - - - rs2891671 8:124051947 A 79139 NM_024295.4 Transcript intron_variant - - - - - - rs2891671 8:124051947 A CCDS47915.1 CCDS47915.1 Transcript intron_variant - - - - - - rs2891671 8:124051947 A 79139 NM_001134671.1 Transcript intron_variant - - - - - - rs2891671 8:124051947 A ENSESTG00000023361 ENSESTT00000059179 Transcript intron_variant - - - - - - rs2891671 8:124051947 A ENSESTG00000023361 ENSESTT00000059161 Transcript intron_variant - - - - - - rs2891671 8:124051947 A ENSESTG00000022426 ENSESTT00000056640 Transcript upstream_gene_variant - - - - - - DISTANCE=2261 rs1351773 8:124426231 A - ENSR00001400597 RegulatoryFeature regulatory_region_variant - - - - - - rs1351773 8:124426231 A ENSESTG00000022714 ENSESTT00000057421 Transcript upstream_gene_variant - - - - - - DISTANCE=2783 rs1351773 8:124426231 A ENSESTG00000022714 ENSESTT00000057441 Transcript upstream_gene_variant - - - - - - DISTANCE=2783 rs1351773 8:124426231 A ENSESTG00000022714 ENSESTT00000057399 Transcript upstream_gene_variant - - - - - - DISTANCE=2783 rs1351773 8:124426231 A ENSESTG00000022714 ENSESTT00000057457 Transcript upstream_gene_variant - - - - - - DISTANCE=2814 rs1351773 8:124426231 A ENSESTG00000022714 ENSESTT00000057377 Transcript upstream_gene_variant - - - - - - DISTANCE=2782 rs1351773 8:124426231 A ENSESTG00000022714 ENSESTT00000057407 Transcript upstream_gene_variant - - - - - - DISTANCE=2783 rs1351773 8:124426231 A 55093 NM_018024.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2734 rs1351773 8:124426231 A CCDS6344.1 CCDS6344.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2859 rs12679800 8:124432117 G ENSESTG00000022714 ENSESTT00000057421 Transcript intron_variant - - - - - - rs12679800 8:124432117 G ENSESTG00000022714 ENSESTT00000057441 Transcript intron_variant - - - - - - rs12679800 8:124432117 G ENSESTG00000022714 ENSESTT00000057399 Transcript intron_variant - - - - - - rs12679800 8:124432117 G ENSESTG00000022714 ENSESTT00000057457 Transcript intron_variant - - - - - - rs12679800 8:124432117 G ENSESTG00000022714 ENSESTT00000057377 Transcript intron_variant - - - - - - rs12679800 8:124432117 G ENSESTG00000022714 ENSESTT00000057407 Transcript intron_variant - - - - - - rs12679800 8:124432117 G 55093 NM_018024.1 Transcript intron_variant - - - - - - rs12679800 8:124432117 G CCDS6344.1 CCDS6344.1 Transcript intron_variant - - - - - - rs7006079 8:124587719 G - - - intergenic_variant - - - - - - rs7013195 8:124885857 A 654463 NM_001039112.2 Transcript intron_variant - - - - - - rs6993248 8:124885858 A 654463 NM_001039112.2 Transcript intron_variant - - - - - - rs7460460 8:125434094 A - - - intergenic_variant - - - - - - rs3116112 8:125672503 A - ENSR00001400894 RegulatoryFeature regulatory_region_variant - - - - - - rs3116112 8:125672503 A CCDS6353.1 CCDS6353.1 Transcript intron_variant - - - - - - rs3116112 8:125672503 A 9788 NM_014751.4 Transcript intron_variant - - - - - - rs3110531 8:125672571 A - ENSR00001400894 RegulatoryFeature regulatory_region_variant - - - - - - rs3110531 8:125672571 A CCDS6353.1 CCDS6353.1 Transcript intron_variant - - - - - - rs3110531 8:125672571 A 9788 NM_014751.4 Transcript intron_variant - - - - - - rs3109482 8:125721138 C ENSESTG00000033682 ENSESTT00000085133 Transcript intron_variant - - - - - - rs3109482 8:125721138 C CCDS6353.1 CCDS6353.1 Transcript intron_variant - - - - - - rs3109482 8:125721138 C 9788 NM_014751.4 Transcript intron_variant - - - - - - rs10103776 8:126295642 G - ENSR00001401065 RegulatoryFeature regulatory_region_variant - - - - - - rs10103776 8:126295642 G ENSESTG00000033459 ENSESTT00000084571 Transcript intron_variant - - - - - - rs10103776 8:126295642 G 286053 NM_173685.2 Transcript intron_variant - - - - - - rs10103776 8:126295642 G ENSESTG00000033459 ENSESTT00000084586 Transcript intron_variant - - - - - - rs10103776 8:126295642 G CCDS6356.1 CCDS6356.1 Transcript intron_variant - - - - - - rs3919792 8:126604661 G - ENSR00001445227 RegulatoryFeature regulatory_region_variant - - - - - - rs3919792 8:126604661 G - - - intergenic_variant - - - - - - rs6470370 8:126660448 T - ENSR00001401213 RegulatoryFeature regulatory_region_variant - - - - - - rs6470370 8:126660448 T - - - intergenic_variant - - - - - - rs10111349 8:126746242 T - - - intergenic_variant - - - - - - rs6995286 8:126905201 T - - - intergenic_variant - - - - - - rs10088558 8:127055154 A - - - intergenic_variant - - - - - - rs4394355 8:127297881 T - - - intergenic_variant - - - - - - rs3999772 8:128475554 T 727677 NR_024393.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2042008 8:129192969 A - - - intergenic_variant - - - - - - rs4733861 8:129377198 C - - - intergenic_variant - - - - - - rs6470628 8:129442292 G ENSESTG00000013173 ENSESTT00000033057 Transcript intron_variant - - - - - - rs6470628 8:129442292 G ENSESTG00000001963 ENSESTT00000004875 Transcript upstream_gene_variant - - - - - - DISTANCE=1651 rs6470628 8:129442292 G ENSESTG00000001963 ENSESTT00000004873 Transcript intron_variant - - - - - - rs6470628 8:129442292 G ENSESTG00000001963 ENSESTT00000004870 Transcript intron_variant - - - - - - rs6470628 8:129442292 G ENSESTG00000001963 ENSESTT00000004888 Transcript upstream_gene_variant - - - - - - DISTANCE=1960 rs1516965 8:129495352 C ENSESTG00000013173 ENSESTT00000033057 Transcript intron_variant - - - - - - rs1516965 8:129495352 C ENSESTG00000013180 ENSESTT00000033064 Transcript intron_variant - - - - - - rs1516965 8:129495352 C ENSESTG00000001963 ENSESTT00000004873 Transcript intron_variant - - - - - - rs1516965 8:129495352 C ENSESTG00000001963 ENSESTT00000004870 Transcript intron_variant - - - - - - rs1516979 8:129506116 T ENSESTG00000013173 ENSESTT00000033057 Transcript intron_variant - - - - - - rs1516979 8:129506116 T ENSESTG00000013180 ENSESTT00000033064 Transcript upstream_gene_variant - - - - - - DISTANCE=3084 rs1516979 8:129506116 T ENSESTG00000001963 ENSESTT00000004873 Transcript intron_variant - - - - - - rs1516979 8:129506116 T ENSESTG00000001963 ENSESTT00000004870 Transcript intron_variant - - - - - - rs7836008 8:129512382 G - ENSR00001401811 RegulatoryFeature regulatory_region_variant - - - - - - rs7836008 8:129512382 G ENSESTG00000013173 ENSESTT00000033057 Transcript intron_variant - - - - - - rs7836008 8:129512382 G ENSESTG00000001963 ENSESTT00000004873 Transcript intron_variant - - - - - - rs7836008 8:129512382 G ENSESTG00000001963 ENSESTT00000004870 Transcript intron_variant - - - - - - rs7011166 8:129865700 C - - - intergenic_variant - - - - - - rs1119881 8:129941334 A - - - intergenic_variant - - - - - - rs10088651 8:129985872 G - ENSR00001445552 RegulatoryFeature regulatory_region_variant - - - - - - rs10088651 8:129985872 G - - - intergenic_variant - - - - - - rs6470704 8:130201992 G - - - intergenic_variant - - - - - - rs2929845 8:130922650 C - ENSR00001402076 RegulatoryFeature regulatory_region_variant - - - - - - rs2929845 8:130922650 C ENSESTG00000025137 ENSESTT00000063407 Transcript intron_variant - - - - - - rs2929845 8:130922650 C 51571 NM_001256763.1 Transcript intron_variant - - - - - - rs2929845 8:130922650 C ENSESTG00000025137 ENSESTT00000063545 Transcript intron_variant - - - - - - rs2929845 8:130922650 C ENSESTG00000025137 ENSESTT00000063454 Transcript intron_variant - - - - - - rs2929845 8:130922650 C 51571 NR_046359.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2929845 8:130922650 C ENSESTG00000025137 ENSESTT00000063603 Transcript intron_variant - - - - - - rs2929845 8:130922650 C 51571 NM_016623.4 Transcript intron_variant - - - - - - rs2929845 8:130922650 C 51571 NR_046360.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2929845 8:130922650 C 51571 NR_046361.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2929845 8:130922650 C ENSESTG00000025137 ENSESTT00000063475 Transcript intron_variant - - - - - - rs2929844 8:130924499 A ENSESTG00000025137 ENSESTT00000063407 Transcript intron_variant - - - - - - rs2929844 8:130924499 A 51571 NM_001256763.1 Transcript intron_variant - - - - - - rs2929844 8:130924499 A ENSESTG00000025137 ENSESTT00000063545 Transcript intron_variant - - - - - - rs2929844 8:130924499 A ENSESTG00000025137 ENSESTT00000063454 Transcript intron_variant - - - - - - rs2929844 8:130924499 A 51571 NR_046359.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2929844 8:130924499 A ENSESTG00000025137 ENSESTT00000063603 Transcript intron_variant - - - - - - rs2929844 8:130924499 A 51571 NM_016623.4 Transcript intron_variant - - - - - - rs2929844 8:130924499 A 51571 NR_046360.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2929844 8:130924499 A 51571 NR_046361.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2929844 8:130924499 A ENSESTG00000025137 ENSESTT00000063475 Transcript intron_variant - - - - - - rs2954994 8:130924501 A ENSESTG00000025137 ENSESTT00000063407 Transcript intron_variant - - - - - - rs2954994 8:130924501 A 51571 NM_001256763.1 Transcript intron_variant - - - - - - rs2954994 8:130924501 A ENSESTG00000025137 ENSESTT00000063545 Transcript intron_variant - - - - - - rs2954994 8:130924501 A ENSESTG00000025137 ENSESTT00000063454 Transcript intron_variant - - - - - - rs2954994 8:130924501 A 51571 NR_046359.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2954994 8:130924501 A ENSESTG00000025137 ENSESTT00000063603 Transcript intron_variant - - - - - - rs2954994 8:130924501 A 51571 NM_016623.4 Transcript intron_variant - - - - - - rs2954994 8:130924501 A 51571 NR_046360.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2954994 8:130924501 A 51571 NR_046361.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2954994 8:130924501 A ENSESTG00000025137 ENSESTT00000063475 Transcript intron_variant - - - - - - rs4557719 8:131669449 C - - - intergenic_variant - - - - - - rs6415532 8:132227035 T - - - intergenic_variant - - - - - - rs273424 8:132496672 T - - - intergenic_variant - - - - - - rs2922727 8:132538058 C - - - intergenic_variant - - - - - - rs1594333 8:132540047 A - - - intergenic_variant - - - - - - rs11780143 8:132864849 T - - - intergenic_variant - - - - - - rs12546265 8:132866056 G - - - intergenic_variant - - - - - - rs4269523 8:132959390 C - ENSR00001402397 RegulatoryFeature regulatory_region_variant - - - - - - rs4269523 8:132959390 C ENSESTG00000012801 ENSESTT00000032214 Transcript intron_variant - - - - - - rs4269523 8:132959390 C 23167 NM_015137.4 Transcript intron_variant - - - - - - rs4269523 8:132959390 C CCDS34942.2 CCDS34942.2 Transcript intron_variant - - - - - - rs4269523 8:132959390 C ENSESTG00000012801 ENSESTT00000032205 Transcript intron_variant - - - - - - rs4269523 8:132959390 C ENSESTG00000012801 ENSESTT00000032212 Transcript intron_variant - - - - - - rs9297842 8:133326226 C CCDS34943.1 CCDS34943.1 Transcript intron_variant - - - - - - rs9297842 8:133326226 C 3786 NM_001204824.1 Transcript intron_variant - - - - - - rs9297842 8:133326226 C CCDS56554.1 CCDS56554.1 Transcript intron_variant - - - - - - rs9297842 8:133326226 C 3786 NM_004519.3 Transcript intron_variant - - - - - - rs10956659 8:133367949 C CCDS34943.1 CCDS34943.1 Transcript intron_variant - - - - - - rs10956659 8:133367949 C 3786 NM_001204824.1 Transcript intron_variant - - - - - - rs10956659 8:133367949 C CCDS56554.1 CCDS56554.1 Transcript intron_variant - - - - - - rs10956659 8:133367949 C 3786 NM_004519.3 Transcript intron_variant - - - - - - rs2721886 8:133478885 T CCDS34943.1 CCDS34943.1 Transcript intron_variant - - - - - - rs2721886 8:133478885 T 3786 NM_004519.3 Transcript intron_variant - - - - - - rs116064213 8:133508480 T ENSESTG00000013237 ENSESTT00000033203 Transcript intron_variant - - - - - - rs2738429 8:133582602 C 23639 NM_012472.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1845 rs2738429 8:133582602 C ENSESTG00000013894 ENSESTT00000034718 Transcript downstream_gene_variant - - - - - - DISTANCE=1847 rs2738429 8:133582602 C ENSESTG00000013894 ENSESTT00000034713 Transcript downstream_gene_variant - - - - - - DISTANCE=1847 rs2738429 8:133582602 C CCDS6365.1 CCDS6365.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1952 rs2738429 8:133582602 C ENSESTG00000013894 ENSESTT00000034731 Transcript downstream_gene_variant - - - - - - DISTANCE=1722 rs2738430 8:133586475 G 23639 NM_012472.3 Transcript intron_variant - - - - - - rs2738430 8:133586475 G ENSESTG00000013894 ENSESTT00000034718 Transcript intron_variant - - - - - - rs2738430 8:133586475 G ENSESTG00000013894 ENSESTT00000034713 Transcript intron_variant - - - - - - rs2738430 8:133586475 G CCDS6365.1 CCDS6365.1 Transcript intron_variant - - - - - - rs2738430 8:133586475 G ENSESTG00000013894 ENSESTT00000034731 Transcript intron_variant - - - - - - rs2733163 8:133594126 C - ENSR00001402451 RegulatoryFeature regulatory_region_variant - - - - - - rs2733163 8:133594126 C 23639 NM_012472.3 Transcript intron_variant - - - - - - rs2733163 8:133594126 C ENSESTG00000013894 ENSESTT00000034718 Transcript intron_variant - - - - - - rs2733163 8:133594126 C ENSESTG00000013894 ENSESTT00000034713 Transcript intron_variant - - - - - - rs2733163 8:133594126 C CCDS6365.1 CCDS6365.1 Transcript intron_variant - - - - - - rs2733163 8:133594126 C ENSESTG00000013894 ENSESTT00000034731 Transcript intron_variant - - - - - - rs2733164 8:133594213 C - ENSR00001402451 RegulatoryFeature regulatory_region_variant - - - - - - rs2733164 8:133594213 C 23639 NM_012472.3 Transcript intron_variant - - - - - - rs2733164 8:133594213 C ENSESTG00000013894 ENSESTT00000034718 Transcript intron_variant - - - - - - rs2733164 8:133594213 C ENSESTG00000013894 ENSESTT00000034713 Transcript intron_variant - - - - - - rs2733164 8:133594213 C CCDS6365.1 CCDS6365.1 Transcript intron_variant - - - - - - rs2733164 8:133594213 C ENSESTG00000013894 ENSESTT00000034731 Transcript intron_variant - - - - - - rs2738434 8:133604901 G 23639 NM_012472.3 Transcript intron_variant - - - - - - rs2738434 8:133604901 G ENSESTG00000013894 ENSESTT00000034718 Transcript intron_variant - - - - - - rs2738434 8:133604901 G ENSESTG00000013894 ENSESTT00000034713 Transcript intron_variant - - - - - - rs2738434 8:133604901 G CCDS6365.1 CCDS6365.1 Transcript intron_variant - - - - - - rs2738434 8:133604901 G ENSESTG00000013894 ENSESTT00000034731 Transcript intron_variant - - - - - - rs10104504 8:133705849 A - - - intergenic_variant - - - - - - rs2553616 8:133751502 G CCDS47921.1 CCDS47921.1 Transcript intron_variant - - - - - - rs2553616 8:133751502 G CCDS6366.1 CCDS6366.1 Transcript intron_variant - - - - - - rs2553616 8:133751502 G ENSESTG00000013814 ENSESTT00000034533 Transcript intron_variant - - - - - - rs2553616 8:133751502 G ENSESTG00000013814 ENSESTT00000034540 Transcript intron_variant - - - - - - rs2553616 8:133751502 G 137835 NM_144649.2 Transcript intron_variant - - - - - - rs2553616 8:133751502 G 137835 NM_001145153.1 Transcript intron_variant - - - - - - rs2553612 8:133761283 C CCDS47921.1 CCDS47921.1 Transcript intron_variant - - - - - - rs2553612 8:133761283 C CCDS6366.1 CCDS6366.1 Transcript intron_variant - - - - - - rs2553612 8:133761283 C ENSESTG00000013814 ENSESTT00000034533 Transcript intron_variant - - - - - - rs2553612 8:133761283 C ENSESTG00000013814 ENSESTT00000034540 Transcript intron_variant - - - - - - rs2553612 8:133761283 C 137835 NM_144649.2 Transcript intron_variant - - - - - - rs2553612 8:133761283 C 137835 NM_001145153.1 Transcript intron_variant - - - - - - rs2739025 8:133761708 C CCDS47921.1 CCDS47921.1 Transcript intron_variant - - - - - - rs2739025 8:133761708 C CCDS6366.1 CCDS6366.1 Transcript intron_variant - - - - - - rs2739025 8:133761708 C ENSESTG00000013814 ENSESTT00000034533 Transcript intron_variant - - - - - - rs2739025 8:133761708 C ENSESTG00000013814 ENSESTT00000034540 Transcript intron_variant - - - - - - rs2739025 8:133761708 C 137835 NM_144649.2 Transcript intron_variant - - - - - - rs2739025 8:133761708 C 137835 NM_001145153.1 Transcript intron_variant - - - - - - rs2553611 8:133761730 T CCDS47921.1 CCDS47921.1 Transcript intron_variant - - - - - - rs2553611 8:133761730 T CCDS6366.1 CCDS6366.1 Transcript intron_variant - - - - - - rs2553611 8:133761730 T ENSESTG00000013814 ENSESTT00000034533 Transcript intron_variant - - - - - - rs2553611 8:133761730 T ENSESTG00000013814 ENSESTT00000034540 Transcript intron_variant - - - - - - rs2553611 8:133761730 T 137835 NM_144649.2 Transcript intron_variant - - - - - - rs2553611 8:133761730 T 137835 NM_001145153.1 Transcript intron_variant - - - - - - rs2553607 8:133770166 G CCDS47921.1 CCDS47921.1 Transcript intron_variant - - - - - - rs2553607 8:133770166 G CCDS6366.1 CCDS6366.1 Transcript intron_variant - - - - - - rs2553607 8:133770166 G ENSESTG00000013814 ENSESTT00000034533 Transcript intron_variant - - - - - - rs2553607 8:133770166 G 137835 NM_144649.2 Transcript intron_variant - - - - - - rs2553607 8:133770166 G 137835 NM_001145153.1 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033287 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033274 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033259 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033261 Transcript intron_variant - - - - - - rs2553586 8:133812994 C 51105 NM_198513.1 Transcript intron_variant - - - - - - rs2553586 8:133812994 C 51105 NM_032205.3 Transcript intron_variant - - - - - - rs2553586 8:133812994 C CCDS6369.2 CCDS6369.2 Transcript intron_variant - - - - - - rs2553586 8:133812994 C CCDS6368.1 CCDS6368.1 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033283 Transcript intron_variant - - - - - - rs2553586 8:133812994 C 51105 NM_016018.4 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033270 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033295 Transcript intron_variant - - - - - - rs2553586 8:133812994 C CCDS6367.2 CCDS6367.2 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033298 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033267 Transcript intron_variant - - - - - - rs2553586 8:133812994 C ENSESTG00000013259 ENSESTT00000033276 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034392 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013391 ENSESTT00000033740 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034382 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034398 Transcript intron_variant - - - - - - rs2702976 8:134092466 A CCDS47922.1 CCDS47922.1 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034404 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034402 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034359 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034388 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034376 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034355 Transcript intron_variant - - - - - - rs2702976 8:134092466 A CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034315 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034400 Transcript intron_variant - - - - - - rs2702976 8:134092466 A 6503 NM_001045556.2 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034370 Transcript intron_variant - - - - - - rs2702976 8:134092466 A 7038 NM_003235.4 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034406 Transcript intron_variant - - - - - - rs2702976 8:134092466 A 6503 NM_001045557.2 Transcript intron_variant - - - - - - rs2702976 8:134092466 A ENSESTG00000013748 ENSESTT00000034350 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034392 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013391 ENSESTT00000033740 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034382 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034398 Transcript intron_variant - - - - - - rs2702980 8:134094438 C CCDS47922.1 CCDS47922.1 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034404 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034402 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034359 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034388 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034376 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034355 Transcript intron_variant - - - - - - rs2702980 8:134094438 C CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034315 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034400 Transcript intron_variant - - - - - - rs2702980 8:134094438 C 6503 NM_001045556.2 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034370 Transcript intron_variant - - - - - - rs2702980 8:134094438 C 7038 NM_003235.4 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034406 Transcript intron_variant - - - - - - rs2702980 8:134094438 C 6503 NM_001045557.2 Transcript intron_variant - - - - - - rs2702980 8:134094438 C ENSESTG00000013748 ENSESTT00000034350 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034392 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013391 ENSESTT00000033740 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034382 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034398 Transcript intron_variant - - - - - - rs2702981 8:134094475 T CCDS47922.1 CCDS47922.1 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034404 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034402 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034359 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034388 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034376 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034355 Transcript intron_variant - - - - - - rs2702981 8:134094475 T CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034315 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034400 Transcript intron_variant - - - - - - rs2702981 8:134094475 T 6503 NM_001045556.2 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034370 Transcript intron_variant - - - - - - rs2702981 8:134094475 T 7038 NM_003235.4 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034406 Transcript intron_variant - - - - - - rs2702981 8:134094475 T 6503 NM_001045557.2 Transcript intron_variant - - - - - - rs2702981 8:134094475 T ENSESTG00000013748 ENSESTT00000034350 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034392 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013391 ENSESTT00000033740 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034382 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034398 Transcript intron_variant - - - - - - rs2702984 8:134096069 G CCDS47922.1 CCDS47922.1 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034404 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034402 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034359 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034388 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034376 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034355 Transcript intron_variant - - - - - - rs2702984 8:134096069 G CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034315 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034400 Transcript intron_variant - - - - - - rs2702984 8:134096069 G 6503 NM_001045556.2 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034370 Transcript intron_variant - - - - - - rs2702984 8:134096069 G 7038 NM_003235.4 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034406 Transcript intron_variant - - - - - - rs2702984 8:134096069 G 6503 NM_001045557.2 Transcript intron_variant - - - - - - rs2702984 8:134096069 G ENSESTG00000013748 ENSESTT00000034350 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034392 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013391 ENSESTT00000033740 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034382 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034398 Transcript intron_variant - - - - - - rs2739174 8:134101174 A CCDS47922.1 CCDS47922.1 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034404 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034402 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034359 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034388 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034376 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034355 Transcript intron_variant - - - - - - rs2739174 8:134101174 A CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034315 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034400 Transcript intron_variant - - - - - - rs2739174 8:134101174 A 6503 NM_001045556.2 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034370 Transcript intron_variant - - - - - - rs2739174 8:134101174 A 7038 NM_003235.4 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034406 Transcript intron_variant - - - - - - rs2739174 8:134101174 A 6503 NM_001045557.2 Transcript intron_variant - - - - - - rs2739174 8:134101174 A ENSESTG00000013748 ENSESTT00000034350 Transcript intron_variant - - - - - - rs2979043 8:134126016 G ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2979043 8:134126016 G ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2979043 8:134126016 G ENSESTG00000013748 ENSESTT00000034315 Transcript intron_variant - - - - - - rs2979043 8:134126016 G CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2979043 8:134126016 G 7038 NM_003235.4 Transcript intron_variant - - - - - - rs2958682 8:134126033 G ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2958682 8:134126033 G ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2958682 8:134126033 G ENSESTG00000013748 ENSESTT00000034315 Transcript intron_variant - - - - - - rs2958682 8:134126033 G CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2958682 8:134126033 G 7038 NM_003235.4 Transcript intron_variant - - - - - - rs2958689 8:134134068 T ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2958689 8:134134068 T ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2958689 8:134134068 T ENSESTG00000013748 ENSESTT00000034315 Transcript intron_variant - - - - - - rs2958689 8:134134068 T CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2958689 8:134134068 T 7038 NM_003235.4 Transcript intron_variant - - - - - - rs2958690 8:134134072 T ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2958690 8:134134072 T ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2958690 8:134134072 T ENSESTG00000013748 ENSESTT00000034315 Transcript intron_variant - - - - - - rs2958690 8:134134072 T CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2958690 8:134134072 T 7038 NM_003235.4 Transcript intron_variant - - - - - - rs2958698 8:134141220 T - ENSR00001445846 RegulatoryFeature regulatory_region_variant - - - - - - rs2958698 8:134141220 T ENSESTG00000013391 ENSESTT00000033725 Transcript intron_variant - - - - - - rs2958698 8:134141220 T ENSESTG00000013391 ENSESTT00000033738 Transcript intron_variant - - - - - - rs2958698 8:134141220 T ENSESTG00000013748 ENSESTT00000034315 Transcript synonymous_variant 231 174 58 P ccG/ccA - rs2958698 8:134141220 T ENSESTG00000013391 ENSESTT00000033744 Transcript upstream_gene_variant - - - - - - DISTANCE=4493 rs2958698 8:134141220 T CCDS34944.1 CCDS34944.1 Transcript intron_variant - - - - - - rs2958698 8:134141220 T 7038 NM_003235.4 Transcript intron_variant - - - - - - rs10095872 8:134160027 A - ENSR00001445851 RegulatoryFeature regulatory_region_variant - - - - - - rs10095872 8:134160027 A - - - intergenic_variant - - - - - - rs2737698 8:134174611 G - ENSR00001445854 RegulatoryFeature regulatory_region_variant - - - - - - rs2737698 8:134174611 G - - - intergenic_variant - - - - - - rs7010243 8:134190614 C - ENSR00001445858 RegulatoryFeature regulatory_region_variant - - - - - - rs7010243 8:134190614 C - - - intergenic_variant - - - - - - rs7010393 8:134190717 C - ENSR00001445858 RegulatoryFeature regulatory_region_variant - - - - - - rs7010393 8:134190717 C - - - intergenic_variant - - - - - - rs7015261 8:134191127 C - - - intergenic_variant - - - - - - rs4461887 8:134191833 A - - - intergenic_variant - - - - - - rs2977524 8:134212717 C ENSESTG00000013553 ENSESTT00000033918 Transcript intron_variant - - - - - - rs2977524 8:134212717 C ENSESTG00000013553 ENSESTT00000033922 Transcript intron_variant - - - - - - rs2977524 8:134212717 C 8840 NM_001204870.1 Transcript intron_variant - - - - - - rs2977524 8:134212717 C 8840 NM_003882.3 Transcript intron_variant - - - - - - rs2977524 8:134212717 C CCDS6371.1 CCDS6371.1 Transcript intron_variant - - - - - - rs2977524 8:134212717 C CCDS56555.1 CCDS56555.1 Transcript intron_variant - - - - - - rs2977524 8:134212717 C 8840 NM_001204869.1 Transcript intron_variant - - - - - - rs2977524 8:134212717 C 8840 NM_080838.2 Transcript intron_variant - - - - - - rs2977524 8:134212717 C ENSESTG00000013553 ENSESTT00000033907 Transcript intron_variant - - - - - - rs2977524 8:134212717 C CCDS6372.1 CCDS6372.1 Transcript intron_variant - - - - - - rs2977524 8:134212717 C CCDS56556.1 CCDS56556.1 Transcript intron_variant - - - - - - rs2977524 8:134212717 C 8840 NR_037944.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4304316 8:134213130 C ENSESTG00000013553 ENSESTT00000033918 Transcript intron_variant - - - - - - rs4304316 8:134213130 C ENSESTG00000013553 ENSESTT00000033922 Transcript intron_variant - - - - - - rs4304316 8:134213130 C 8840 NM_001204870.1 Transcript intron_variant - - - - - - rs4304316 8:134213130 C 8840 NM_003882.3 Transcript intron_variant - - - - - - rs4304316 8:134213130 C CCDS6371.1 CCDS6371.1 Transcript intron_variant - - - - - - rs4304316 8:134213130 C CCDS56555.1 CCDS56555.1 Transcript intron_variant - - - - - - rs4304316 8:134213130 C 8840 NM_001204869.1 Transcript intron_variant - - - - - - rs4304316 8:134213130 C 8840 NM_080838.2 Transcript intron_variant - - - - - - rs4304316 8:134213130 C ENSESTG00000013553 ENSESTT00000033907 Transcript intron_variant - - - - - - rs4304316 8:134213130 C CCDS6372.1 CCDS6372.1 Transcript intron_variant - - - - - - rs4304316 8:134213130 C CCDS56556.1 CCDS56556.1 Transcript intron_variant - - - - - - rs4304316 8:134213130 C 8840 NR_037944.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2977528 8:134214488 C ENSESTG00000013553 ENSESTT00000033918 Transcript intron_variant - - - - - - rs2977528 8:134214488 C ENSESTG00000013553 ENSESTT00000033922 Transcript intron_variant - - - - - - rs2977528 8:134214488 C 8840 NM_001204870.1 Transcript intron_variant - - - - - - rs2977528 8:134214488 C 8840 NM_003882.3 Transcript intron_variant - - - - - - rs2977528 8:134214488 C CCDS6371.1 CCDS6371.1 Transcript intron_variant - - - - - - rs2977528 8:134214488 C CCDS56555.1 CCDS56555.1 Transcript intron_variant - - - - - - rs2977528 8:134214488 C 8840 NM_001204869.1 Transcript intron_variant - - - - - - rs2977528 8:134214488 C 8840 NM_080838.2 Transcript intron_variant - - - - - - rs2977528 8:134214488 C ENSESTG00000013553 ENSESTT00000033907 Transcript intron_variant - - - - - - rs2977528 8:134214488 C CCDS6372.1 CCDS6372.1 Transcript intron_variant - - - - - - rs2977528 8:134214488 C CCDS56556.1 CCDS56556.1 Transcript intron_variant - - - - - - rs2977528 8:134214488 C 8840 NR_037944.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2977534 8:134219061 C ENSESTG00000013553 ENSESTT00000033918 Transcript intron_variant - - - - - - rs2977534 8:134219061 C ENSESTG00000013553 ENSESTT00000033922 Transcript intron_variant - - - - - - rs2977534 8:134219061 C 8840 NM_001204870.1 Transcript intron_variant - - - - - - rs2977534 8:134219061 C 8840 NM_003882.3 Transcript intron_variant - - - - - - rs2977534 8:134219061 C CCDS6371.1 CCDS6371.1 Transcript intron_variant - - - - - - rs2977534 8:134219061 C CCDS56555.1 CCDS56555.1 Transcript intron_variant - - - - - - rs2977534 8:134219061 C 8840 NM_001204869.1 Transcript intron_variant - - - - - - rs2977534 8:134219061 C 8840 NM_080838.2 Transcript intron_variant - - - - - - rs2977534 8:134219061 C ENSESTG00000013553 ENSESTT00000033907 Transcript intron_variant - - - - - - rs2977534 8:134219061 C CCDS6372.1 CCDS6372.1 Transcript intron_variant - - - - - - rs2977534 8:134219061 C CCDS56556.1 CCDS56556.1 Transcript intron_variant - - - - - - rs2977534 8:134219061 C 8840 NR_037944.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs13258091 8:134225434 C ENSESTG00000013553 ENSESTT00000033918 Transcript intron_variant - - - - - - rs13258091 8:134225434 C ENSESTG00000013553 ENSESTT00000033922 Transcript intron_variant - - - - - - rs13258091 8:134225434 C 8840 NM_001204870.1 Transcript intron_variant - - - - - - rs13258091 8:134225434 C 8840 NM_003882.3 Transcript intron_variant - - - - - - rs13258091 8:134225434 C CCDS6371.1 CCDS6371.1 Transcript intron_variant - - - - - - rs13258091 8:134225434 C CCDS56555.1 CCDS56555.1 Transcript intron_variant - - - - - - rs13258091 8:134225434 C 8840 NM_001204869.1 Transcript intron_variant - - - - - - rs13258091 8:134225434 C 8840 NM_080838.2 Transcript intron_variant - - - - - - rs13258091 8:134225434 C ENSESTG00000013553 ENSESTT00000033907 Transcript intron_variant - - - - - - rs13258091 8:134225434 C CCDS6372.1 CCDS6372.1 Transcript intron_variant - - - - - - rs13258091 8:134225434 C CCDS56556.1 CCDS56556.1 Transcript intron_variant - - - - - - rs13258091 8:134225434 C 8840 NR_037944.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7461261 8:134236338 C ENSESTG00000013553 ENSESTT00000033918 Transcript downstream_gene_variant - - - - - - DISTANCE=3420 rs7461261 8:134236338 C ENSESTG00000013553 ENSESTT00000033922 Transcript intron_variant - - - - - - rs7461261 8:134236338 C 8840 NM_001204870.1 Transcript intron_variant - - - - - - rs7461261 8:134236338 C 8840 NM_003882.3 Transcript intron_variant - - - - - - rs7461261 8:134236338 C CCDS6371.1 CCDS6371.1 Transcript intron_variant - - - - - - rs7461261 8:134236338 C CCDS56555.1 CCDS56555.1 Transcript intron_variant - - - - - - rs7461261 8:134236338 C 8840 NM_001204869.1 Transcript intron_variant - - - - - - rs7461261 8:134236338 C 8840 NM_080838.2 Transcript intron_variant - - - - - - rs7461261 8:134236338 C ENSESTG00000013553 ENSESTT00000033907 Transcript intron_variant - - - - - - rs7461261 8:134236338 C CCDS6372.1 CCDS6372.1 Transcript intron_variant - - - - - - rs7461261 8:134236338 C CCDS56556.1 CCDS56556.1 Transcript intron_variant - - - - - - rs7461261 8:134236338 C 8840 NR_037944.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2929968 8:134238856 A ENSESTG00000013553 ENSESTT00000033922 Transcript intron_variant - - - - - - rs2929968 8:134238856 A 8840 NM_001204870.1 Transcript intron_variant - - - - - - rs2929968 8:134238856 A 8840 NM_003882.3 Transcript intron_variant - - - - - - rs2929968 8:134238856 A CCDS6371.1 CCDS6371.1 Transcript intron_variant - - - - - - rs2929968 8:134238856 A CCDS56555.1 CCDS56555.1 Transcript intron_variant - - - - - - rs2929968 8:134238856 A 8840 NM_001204869.1 Transcript intron_variant - - - - - - rs2929968 8:134238856 A 8840 NM_080838.2 Transcript intron_variant - - - - - - rs2929968 8:134238856 A ENSESTG00000013553 ENSESTT00000033907 Transcript intron_variant - - - - - - rs2929968 8:134238856 A CCDS6372.1 CCDS6372.1 Transcript intron_variant - - - - - - rs2929968 8:134238856 A CCDS56556.1 CCDS56556.1 Transcript intron_variant - - - - - - rs2929968 8:134238856 A 8840 NR_037944.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2977556 8:134248720 C - ENSR00001445872 RegulatoryFeature regulatory_region_variant - - - - - - rs2977556 8:134248720 C ENSESTG00000013606 ENSESTT00000034119 Transcript downstream_gene_variant - - - - - - DISTANCE=2036 rs2977556 8:134248720 C CCDS59113.1 CCDS59113.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2401 rs2977556 8:134248720 C 10397 NM_001258432.1 Transcript downstream_gene_variant - - - - - - DISTANCE=694 rs2977556 8:134248720 C ENSESTG00000013606 ENSESTT00000034142 Transcript downstream_gene_variant - - - - - - DISTANCE=2397 rs2977556 8:134248720 C ENSESTG00000013592 ENSESTT00000033990 Transcript upstream_gene_variant - - - - - - DISTANCE=2078 rs2977556 8:134248720 C CCDS34945.1 CCDS34945.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2401 rs2977556 8:134248720 C 10397 NM_006096.3 Transcript downstream_gene_variant - - - - - - DISTANCE=694 rs2977556 8:134248720 C ENSESTG00000013606 ENSESTT00000034190 Transcript downstream_gene_variant - - - - - - DISTANCE=695 rs2977556 8:134248720 C 8840 NM_080838.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4787 rs2977556 8:134248720 C ENSESTG00000013606 ENSESTT00000034150 Transcript downstream_gene_variant - - - - - - DISTANCE=2594 rs2977556 8:134248720 C CCDS59112.1 CCDS59112.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2401 rs2977556 8:134248720 C 10397 NM_001258433.1 Transcript downstream_gene_variant - - - - - - DISTANCE=694 rs2977556 8:134248720 C ENSESTG00000013606 ENSESTT00000034125 Transcript downstream_gene_variant - - - - - - DISTANCE=1909 rs2977556 8:134248720 C 10397 NM_001135242.1 Transcript downstream_gene_variant - - - - - - DISTANCE=694 rs2977556 8:134248720 C 8840 NM_003882.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4787 rs2977556 8:134248720 C 8840 NM_001204870.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4787 rs2977556 8:134248720 C ENSESTG00000013606 ENSESTT00000034166 Transcript downstream_gene_variant - - - - - - DISTANCE=2402 rs2977556 8:134248720 C 8840 NM_001204869.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4787 rs2977556 8:134248720 C ENSESTG00000013606 ENSESTT00000034161 Transcript downstream_gene_variant - - - - - - DISTANCE=1688 rs2977556 8:134248720 C 8840 NR_037944.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4787 rs2929976 8:134251449 C - ENSR00001445873 RegulatoryFeature regulatory_region_variant - - - - - - rs2929976 8:134251449 C ENSESTG00000013606 ENSESTT00000034119 Transcript intron_variant - - - - - - rs2929976 8:134251449 C CCDS59113.1 CCDS59113.1 Transcript intron_variant - - - - - - rs2929976 8:134251449 C ENSESTG00000013606 ENSESTT00000034150 Transcript intron_variant - - - - - - rs2929976 8:134251449 C 10397 NM_001258432.1 Transcript intron_variant - - - - - - rs2929976 8:134251449 C CCDS59112.1 CCDS59112.1 Transcript intron_variant - - - - - - rs2929976 8:134251449 C ENSESTG00000013606 ENSESTT00000034142 Transcript intron_variant - - - - - - rs2929976 8:134251449 C 10397 NM_001258433.1 Transcript intron_variant - - - - - - rs2929976 8:134251449 C ENSESTG00000013592 ENSESTT00000033990 Transcript intron_variant - - - - - - rs2929976 8:134251449 C ENSESTG00000013606 ENSESTT00000034125 Transcript intron_variant - - - - - - rs2929976 8:134251449 C CCDS34945.1 CCDS34945.1 Transcript intron_variant - - - - - - rs2929976 8:134251449 C ENSESTG00000013606 ENSESTT00000034166 Transcript intron_variant - - - - - - rs2929976 8:134251449 C 10397 NM_001135242.1 Transcript intron_variant - - - - - - rs2929976 8:134251449 C 10397 NM_006096.3 Transcript intron_variant - - - - - - rs2929976 8:134251449 C ENSESTG00000013606 ENSESTT00000034190 Transcript intron_variant - - - - - - rs2929976 8:134251449 C ENSESTG00000013606 ENSESTT00000034161 Transcript intron_variant - - - - - - rs2929977 8:134253794 C - ENSR00001445875 RegulatoryFeature regulatory_region_variant - - - - - - rs2929977 8:134253794 C ENSESTG00000013606 ENSESTT00000034119 Transcript intron_variant - - - - - - rs2929977 8:134253794 C CCDS59113.1 CCDS59113.1 Transcript intron_variant - - - - - - rs2929977 8:134253794 C 10397 NM_001258432.1 Transcript intron_variant - - - - - - rs2929977 8:134253794 C ENSESTG00000013606 ENSESTT00000034142 Transcript intron_variant - - - - - - rs2929977 8:134253794 C ENSESTG00000013592 ENSESTT00000033990 Transcript intron_variant - - - - - - rs2929977 8:134253794 C CCDS34945.1 CCDS34945.1 Transcript intron_variant - - - - - - rs2929977 8:134253794 C 10397 NM_006096.3 Transcript intron_variant - - - - - - rs2929977 8:134253794 C ENSESTG00000013606 ENSESTT00000034190 Transcript intron_variant - - - - - - rs2929977 8:134253794 C ENSESTG00000013606 ENSESTT00000034150 Transcript intron_variant - - - - - - rs2929977 8:134253794 C CCDS59112.1 CCDS59112.1 Transcript intron_variant - - - - - - rs2929977 8:134253794 C 10397 NM_001258433.1 Transcript intron_variant - - - - - - rs2929977 8:134253794 C ENSESTG00000013606 ENSESTT00000034125 Transcript intron_variant - - - - - - rs2929977 8:134253794 C 10397 NM_001135242.1 Transcript intron_variant - - - - - - rs2929977 8:134253794 C ENSESTG00000013606 ENSESTT00000034166 Transcript intron_variant - - - - - - rs2929977 8:134253794 C ENSESTG00000013606 ENSESTT00000034157 Transcript downstream_gene_variant - - - - - - DISTANCE=2820 rs2929977 8:134253794 C ENSESTG00000013606 ENSESTT00000034161 Transcript intron_variant - - - - - - rs2929980 8:134256790 C - ENSR00001445880 RegulatoryFeature regulatory_region_variant - - - - - - rs2929980 8:134256790 C ENSESTG00000013606 ENSESTT00000034119 Transcript intron_variant - - - - - - rs2929980 8:134256790 C CCDS59113.1 CCDS59113.1 Transcript intron_variant - - - - - - rs2929980 8:134256790 C 10397 NM_001258432.1 Transcript intron_variant - - - - - - rs2929980 8:134256790 C ENSESTG00000013606 ENSESTT00000034142 Transcript intron_variant - - - - - - rs2929980 8:134256790 C ENSESTG00000013592 ENSESTT00000033990 Transcript intron_variant - - - - - - rs2929980 8:134256790 C CCDS34945.1 CCDS34945.1 Transcript intron_variant - - - - - - rs2929980 8:134256790 C 10397 NM_006096.3 Transcript intron_variant - - - - - - rs2929980 8:134256790 C ENSESTG00000013606 ENSESTT00000034190 Transcript intron_variant - - - - - - rs2929980 8:134256790 C ENSESTG00000013606 ENSESTT00000034150 Transcript intron_variant - - - - - - rs2929980 8:134256790 C CCDS59112.1 CCDS59112.1 Transcript intron_variant - - - - - - rs2929980 8:134256790 C 10397 NM_001258433.1 Transcript intron_variant - - - - - - rs2929980 8:134256790 C ENSESTG00000013606 ENSESTT00000034125 Transcript intron_variant - - - - - - rs2929980 8:134256790 C 10397 NM_001135242.1 Transcript intron_variant - - - - - - rs2929980 8:134256790 C ENSESTG00000013606 ENSESTT00000034166 Transcript intron_variant - - - - - - rs2929980 8:134256790 C ENSESTG00000013606 ENSESTT00000034115 Transcript downstream_gene_variant - - - - - - DISTANCE=2069 rs2929980 8:134256790 C ENSESTG00000013606 ENSESTT00000034157 Transcript intron_variant - - - - - - rs2929980 8:134256790 C ENSESTG00000013606 ENSESTT00000034161 Transcript intron_variant - - - - - - rs4288360 8:134257328 C ENSESTG00000013606 ENSESTT00000034119 Transcript intron_variant - - - - - - rs4288360 8:134257328 C CCDS59113.1 CCDS59113.1 Transcript intron_variant - - - - - - rs4288360 8:134257328 C 10397 NM_001258432.1 Transcript intron_variant - - - - - - rs4288360 8:134257328 C ENSESTG00000013606 ENSESTT00000034142 Transcript intron_variant - - - - - - rs4288360 8:134257328 C ENSESTG00000013592 ENSESTT00000033990 Transcript intron_variant - - - - - - rs4288360 8:134257328 C CCDS34945.1 CCDS34945.1 Transcript intron_variant - - - - - - rs4288360 8:134257328 C 10397 NM_006096.3 Transcript intron_variant - - - - - - rs4288360 8:134257328 C ENSESTG00000013606 ENSESTT00000034190 Transcript intron_variant - - - - - - rs4288360 8:134257328 C ENSESTG00000013606 ENSESTT00000034150 Transcript intron_variant - - - - - - rs4288360 8:134257328 C CCDS59112.1 CCDS59112.1 Transcript intron_variant - - - - - - rs4288360 8:134257328 C 10397 NM_001258433.1 Transcript intron_variant - - - - - - rs4288360 8:134257328 C ENSESTG00000013606 ENSESTT00000034125 Transcript intron_variant - - - - - - rs4288360 8:134257328 C 10397 NM_001135242.1 Transcript intron_variant - - - - - - rs4288360 8:134257328 C ENSESTG00000013606 ENSESTT00000034166 Transcript intron_variant - - - - - - rs4288360 8:134257328 C ENSESTG00000013606 ENSESTT00000034115 Transcript downstream_gene_variant - - - - - - DISTANCE=1531 rs4288360 8:134257328 C ENSESTG00000013606 ENSESTT00000034157 Transcript intron_variant - - - - - - rs4288360 8:134257328 C ENSESTG00000013606 ENSESTT00000034161 Transcript intron_variant - - - - - - rs2929993 8:134284683 G - ENSR00001445898 RegulatoryFeature regulatory_region_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034119 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034174 Transcript intron_variant - - - - - - rs2929993 8:134284683 G 10397 NM_001258432.1 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034142 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013592 ENSESTT00000033990 Transcript intron_variant - - - - - - rs2929993 8:134284683 G CCDS34945.1 CCDS34945.1 Transcript intron_variant - - - - - - rs2929993 8:134284683 G 10397 NM_006096.3 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034190 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034150 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034087 Transcript intron_variant - - - - - - rs2929993 8:134284683 G 10397 NM_001258433.1 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034125 Transcript intron_variant - - - - - - rs2929993 8:134284683 G 10397 NM_001135242.1 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034166 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034115 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034157 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034075 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034161 Transcript intron_variant - - - - - - rs2929993 8:134284683 G ENSESTG00000013606 ENSESTT00000034065 Transcript intron_variant - - - - - - rs6980722 8:134292015 C - ENSR00001402574 RegulatoryFeature regulatory_region_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034119 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034174 Transcript intron_variant - - - - - - rs6980722 8:134292015 C 10397 NM_001258432.1 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034142 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013592 ENSESTT00000033990 Transcript intron_variant - - - - - - rs6980722 8:134292015 C CCDS34945.1 CCDS34945.1 Transcript intron_variant - - - - - - rs6980722 8:134292015 C 10397 NM_006096.3 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034190 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034150 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034087 Transcript intron_variant - - - - - - rs6980722 8:134292015 C 10397 NM_001258433.1 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034125 Transcript intron_variant - - - - - - rs6980722 8:134292015 C 10397 NM_001135242.1 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034166 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034115 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034157 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034075 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034161 Transcript intron_variant - - - - - - rs6980722 8:134292015 C ENSESTG00000013606 ENSESTT00000034065 Transcript intron_variant - - - - - - rs2977507 8:134292288 C - ENSR00001402575 RegulatoryFeature regulatory_region_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034119 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034174 Transcript intron_variant - - - - - - rs2977507 8:134292288 C 10397 NM_001258432.1 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034142 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013592 ENSESTT00000033990 Transcript intron_variant - - - - - - rs2977507 8:134292288 C CCDS34945.1 CCDS34945.1 Transcript intron_variant - - - - - - rs2977507 8:134292288 C 10397 NM_006096.3 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034190 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034150 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034087 Transcript intron_variant - - - - - - rs2977507 8:134292288 C 10397 NM_001258433.1 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034125 Transcript intron_variant - - - - - - rs2977507 8:134292288 C 10397 NM_001135242.1 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034166 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034115 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034157 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034075 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034161 Transcript intron_variant - - - - - - rs2977507 8:134292288 C ENSESTG00000013606 ENSESTT00000034065 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034119 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034174 Transcript intron_variant - - - - - - rs2977508 8:134293893 A 10397 NM_001258432.1 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034142 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013592 ENSESTT00000033990 Transcript intron_variant - - - - - - rs2977508 8:134293893 A CCDS34945.1 CCDS34945.1 Transcript intron_variant - - - - - - rs2977508 8:134293893 A 10397 NM_006096.3 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034190 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034150 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034087 Transcript intron_variant - - - - - - rs2977508 8:134293893 A 10397 NM_001258433.1 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034125 Transcript intron_variant - - - - - - rs2977508 8:134293893 A 10397 NM_001135242.1 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034166 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034115 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034157 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034075 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034161 Transcript intron_variant - - - - - - rs2977508 8:134293893 A ENSESTG00000013606 ENSESTT00000034065 Transcript intron_variant - - - - - - rs10093576 8:134322931 A - - - intergenic_variant - - - - - - rs2976587 8:134334125 C - - - intergenic_variant - - - - - - rs4451293 8:134338627 C - - - intergenic_variant - - - - - - rs2929938 8:134344946 G - - - intergenic_variant - - - - - - rs2976561 8:134372170 C - - - intergenic_variant - - - - - - rs12677486 8:134381331 G - - - intergenic_variant - - - - - - rs7463858 8:134381599 C - ENSR00001445914 RegulatoryFeature regulatory_region_variant - - - - - - rs7463858 8:134381599 C - - - intergenic_variant - - - - - - rs2929925 8:134381965 G - - - intergenic_variant - - - - - - rs2976571 8:134383003 C - ENSR00001445915 RegulatoryFeature regulatory_region_variant - - - - - - rs2976571 8:134383003 C - - - intergenic_variant - - - - - - rs2976572 8:134383006 C - ENSR00001445915 RegulatoryFeature regulatory_region_variant - - - - - - rs2976572 8:134383006 C - - - intergenic_variant - - - - - - rs4478554 8:134419598 C - ENSR00001402619 RegulatoryFeature regulatory_region_variant - - - - - - rs4478554 8:134419598 C - - - intergenic_variant - - - - - - rs1356611 8:134546131 C - ENSR00001402652 RegulatoryFeature regulatory_region_variant - - - - - - rs1356611 8:134546131 C 6482 NM_003033.3 Transcript intron_variant - - - - - - rs1356611 8:134546131 C 6482 NM_173344.2 Transcript intron_variant - - - - - - rs1356611 8:134546131 C ENSESTG00000004178 ENSESTT00000010530 Transcript intron_variant - - - - - - rs2945789 8:134578060 A - ENSR00001445934 RegulatoryFeature regulatory_region_variant - - - - - - rs2945789 8:134578060 A 6482 NM_003033.3 Transcript intron_variant - - - - - - rs2945789 8:134578060 A 6482 NM_173344.2 Transcript intron_variant - - - - - - rs2945789 8:134578060 A ENSESTG00000004178 ENSESTT00000010530 Transcript intron_variant - - - - - - rs6980789 8:134653062 A - - - intergenic_variant - - - - - - rs6999214 8:134994735 C - - - intergenic_variant - - - - - - rs6471192 8:135144219 A - - - intergenic_variant - - - - - - rs7826738 8:135464002 A - - - intergenic_variant - - - - - - rs28576491 8:135473925 T - - - intergenic_variant - - - - - - rs4273812 8:135688343 A 57623 NM_001174157.1 Transcript intron_variant - - - - - - rs4273812 8:135688343 A CCDS55276.1 CCDS55276.1 Transcript intron_variant - - - - - - rs4273812 8:135688343 A ENSESTG00000002282 ENSESTT00000005716 Transcript intron_variant - - - - - - rs4273812 8:135688343 A ENSESTG00000002282 ENSESTT00000005694 Transcript intron_variant - - - - - - rs4273812 8:135688343 A 57623 NM_001029939.3 Transcript intron_variant - - - - - - rs4273812 8:135688343 A ENSESTG00000002282 ENSESTT00000005713 Transcript intron_variant - - - - - - rs4273812 8:135688343 A CCDS47924.1 CCDS47924.1 Transcript intron_variant - - - - - - rs4273812 8:135688343 A 57623 NM_001167583.2 Transcript intron_variant - - - - - - rs4273812 8:135688343 A 57623 NM_001174158.1 Transcript intron_variant - - - - - - rs4273812 8:135688343 A 57623 NM_020863.3 Transcript intron_variant - - - - - - rs7812785 8:135801331 C - ENSR00001402842 RegulatoryFeature regulatory_region_variant - - - - - - rs7812785 8:135801331 C - - - intergenic_variant - - - - - - rs2975800 8:135856714 G - - - intergenic_variant - - - - - - rs6577925 8:135877136 G - - - intergenic_variant - - - - - - rs4629905 8:137355146 G - - - intergenic_variant - - - - - - rs1583814 8:137417565 G - - - intergenic_variant - - - - - - rs9324435 8:137511304 T - - - intergenic_variant - - - - - - rs2581560 8:137528756 C - - - intergenic_variant - - - - - - rs2660659 8:137618174 A ENSESTG00000029084 ENSESTT00000073226 Transcript intron_variant - - - - - - rs2974258 8:138153790 G - - - intergenic_variant - - - - - - rs4637880 8:138356694 C - - - intergenic_variant - - - - - - rs2943187 8:138443823 T - - - intergenic_variant - - - - - - rs13259431 8:139100215 C - - - intergenic_variant - - - - - - rs10875420 8:139275490 T ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs10875420 8:139275490 T 51059 NM_015912.3 Transcript intron_variant - - - - - - rs10875420 8:139275490 T ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs10875420 8:139275490 T ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs10875420 8:139275490 T ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs10875420 8:139275490 T ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs10875420 8:139275490 T CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs7819459 8:139275599 G ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs7819459 8:139275599 G 51059 NM_015912.3 Transcript intron_variant - - - - - - rs7819459 8:139275599 G ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs7819459 8:139275599 G ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs7819459 8:139275599 G ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs7819459 8:139275599 G ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs7819459 8:139275599 G CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs7823171 8:139275750 A ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs7823171 8:139275750 A 51059 NM_015912.3 Transcript intron_variant - - - - - - rs7823171 8:139275750 A ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs7823171 8:139275750 A ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs7823171 8:139275750 A ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs7823171 8:139275750 A ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs7823171 8:139275750 A CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs2137351 8:139302468 T ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs2137351 8:139302468 T 51059 NM_015912.3 Transcript intron_variant - - - - - - rs2137351 8:139302468 T ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs2137351 8:139302468 T ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs2137351 8:139302468 T ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs2137351 8:139302468 T ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs2137351 8:139302468 T CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs6577907 8:139313570 T ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs6577907 8:139313570 T 51059 NM_015912.3 Transcript intron_variant - - - - - - rs6577907 8:139313570 T ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs6577907 8:139313570 T ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs6577907 8:139313570 T ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs6577907 8:139313570 T ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs6577907 8:139313570 T CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs907627 8:139354043 G 51059 NM_015912.3 Transcript intron_variant - - - - - - rs907627 8:139354043 G ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs907627 8:139354043 G ENSESTG00000006696 ENSESTT00000016990 Transcript intron_variant - - - - - - rs907627 8:139354043 G ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs907627 8:139354043 G ENSESTG00000006716 ENSESTT00000017024 Transcript intron_variant - - - - - - rs907627 8:139354043 G ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs907627 8:139354043 G ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs907627 8:139354043 G ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs907627 8:139354043 G CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs4909776 8:139362201 A 51059 NM_015912.3 Transcript intron_variant - - - - - - rs4909776 8:139362201 A ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs4909776 8:139362201 A ENSESTG00000006696 ENSESTT00000016990 Transcript intron_variant - - - - - - rs4909776 8:139362201 A ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs4909776 8:139362201 A ENSESTG00000006716 ENSESTT00000017024 Transcript intron_variant - - - - - - rs4909776 8:139362201 A ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs4909776 8:139362201 A ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs4909776 8:139362201 A ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs4909776 8:139362201 A CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs4243889 8:139362304 A 51059 NM_015912.3 Transcript intron_variant - - - - - - rs4243889 8:139362304 A ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs4243889 8:139362304 A ENSESTG00000006696 ENSESTT00000016990 Transcript intron_variant - - - - - - rs4243889 8:139362304 A ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs4243889 8:139362304 A ENSESTG00000006716 ENSESTT00000017024 Transcript intron_variant - - - - - - rs4243889 8:139362304 A ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs4243889 8:139362304 A ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs4243889 8:139362304 A ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs4243889 8:139362304 A CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs4243890 8:139362310 C 51059 NM_015912.3 Transcript intron_variant - - - - - - rs4243890 8:139362310 C ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs4243890 8:139362310 C ENSESTG00000006696 ENSESTT00000016990 Transcript intron_variant - - - - - - rs4243890 8:139362310 C ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs4243890 8:139362310 C ENSESTG00000006716 ENSESTT00000017024 Transcript intron_variant - - - - - - rs4243890 8:139362310 C ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs4243890 8:139362310 C ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs4243890 8:139362310 C ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs4243890 8:139362310 C CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs4243891 8:139374686 G 51059 NM_015912.3 Transcript intron_variant - - - - - - rs4243891 8:139374686 G ENSESTG00000006696 ENSESTT00000017013 Transcript intron_variant - - - - - - rs4243891 8:139374686 G ENSESTG00000006696 ENSESTT00000016990 Transcript intron_variant - - - - - - rs4243891 8:139374686 G ENSESTG00000006696 ENSESTT00000017018 Transcript intron_variant - - - - - - rs4243891 8:139374686 G ENSESTG00000006716 ENSESTT00000017024 Transcript intron_variant - - - - - - rs4243891 8:139374686 G ENSESTG00000006696 ENSESTT00000016997 Transcript intron_variant - - - - - - rs4243891 8:139374686 G ENSESTG00000006696 ENSESTT00000017008 Transcript intron_variant - - - - - - rs4243891 8:139374686 G ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs4243891 8:139374686 G CCDS6375.2 CCDS6375.2 Transcript intron_variant - - - - - - rs4909792 8:139437885 C - ENSR00001403089 RegulatoryFeature regulatory_region_variant - - - - - - rs4909792 8:139437885 C 51059 NM_015912.3 Transcript intron_variant - - - - - - rs4909792 8:139437885 C ENSESTG00000006716 ENSESTT00000017024 Transcript intron_variant - - - - - - rs4909792 8:139437885 C ENSESTG00000006696 ENSESTT00000016997 Transcript upstream_gene_variant - - - - - - DISTANCE=127 rs4909792 8:139437885 C ENSESTG00000006696 ENSESTT00000016986 Transcript intron_variant - - - - - - rs4909792 8:139437885 C ENSESTG00000006696 ENSESTT00000016990 Transcript intron_variant - - - - - - rs28482272 8:139580684 A - - - intergenic_variant - - - - - - rs10107843 8:139821110 C 169044 NM_152888.1 Transcript intron_variant - - - - - - rs10107843 8:139821110 C CCDS6376.1 CCDS6376.1 Transcript intron_variant - - - - - - rs6996524 8:140060317 G - - - intergenic_variant - - - - - - rs7007730 8:140071380 A - - - intergenic_variant - - - - - - rs4736252 8:140354883 C - - - intergenic_variant - - - - - - rs2086032 8:140391293 C - - - intergenic_variant - - - - - - rs2471085 8:140507323 G - - - intergenic_variant - - - - - - rs2447384 8:140537560 C - - - intergenic_variant - - - - - - rs2447393 8:140540916 T - - - intergenic_variant - - - - - - rs2468706 8:140549277 T - - - intergenic_variant - - - - - - rs6578040 8:140689240 G ENSESTG00000004730 ENSESTT00000011962 Transcript intron_variant - - - - - - rs6578040 8:140689240 G 51305 NM_016601.2 Transcript intron_variant - - - - - - rs6578040 8:140689240 G CCDS6377.1 CCDS6377.1 Transcript intron_variant - - - - - - rs199217 8:140727072 G - - - intergenic_variant - - - - - - rs1643988 8:140747117 G ENSESTG00000004694 ENSESTT00000011931 Transcript intron_variant - - - - - - rs1643988 8:140747117 G ENSESTG00000004694 ENSESTT00000011953 Transcript intron_variant - - - - - - rs1643988 8:140747117 G ENSESTG00000004694 ENSESTT00000011938 Transcript intron_variant - - - - - - rs1643988 8:140747117 G 83696 NM_001160372.1 Transcript intron_variant - - - - - - rs1643988 8:140747117 G CCDS34946.1 CCDS34946.1 Transcript intron_variant - - - - - - rs1643988 8:140747117 G ENSESTG00000004694 ENSESTT00000011945 Transcript intron_variant - - - - - - rs1643988 8:140747117 G ENSESTG00000004694 ENSESTT00000011928 Transcript intron_variant - - - - - - rs1643988 8:140747117 G ENSESTG00000004694 ENSESTT00000011888 Transcript intron_variant - - - - - - rs1643988 8:140747117 G ENSESTG00000004694 ENSESTT00000011896 Transcript intron_variant - - - - - - rs1643988 8:140747117 G ENSESTG00000004694 ENSESTT00000011944 Transcript intron_variant - - - - - - rs1643988 8:140747117 G 83696 NM_031466.5 Transcript intron_variant - - - - - - rs1643988 8:140747117 G ENSESTG00000004694 ENSESTT00000011903 Transcript intron_variant - - - - - - rs1643988 8:140747117 G CCDS55278.1 CCDS55278.1 Transcript intron_variant - - - - - - rs6578066 8:141079093 C 83696 NM_001160372.1 Transcript intron_variant - - - - - - rs6578066 8:141079093 C CCDS34946.1 CCDS34946.1 Transcript intron_variant - - - - - - rs6578066 8:141079093 C ENSESTG00000004694 ENSESTT00000011917 Transcript intron_variant - - - - - - rs6578066 8:141079093 C ENSESTG00000004694 ENSESTT00000011928 Transcript intron_variant - - - - - - rs6578066 8:141079093 C ENSESTG00000004694 ENSESTT00000011888 Transcript intron_variant - - - - - - rs6578066 8:141079093 C ENSESTG00000004694 ENSESTT00000011896 Transcript intron_variant - - - - - - rs6578066 8:141079093 C 83696 NM_031466.5 Transcript intron_variant - - - - - - rs6578066 8:141079093 C ENSESTG00000004694 ENSESTT00000011911 Transcript intron_variant - - - - - - rs6578066 8:141079093 C ENSESTG00000004694 ENSESTT00000011903 Transcript intron_variant - - - - - - rs6578066 8:141079093 C CCDS55278.1 CCDS55278.1 Transcript intron_variant - - - - - - rs6990801 8:141162145 C 83696 NM_001160372.1 Transcript intron_variant - - - - - - rs6990801 8:141162145 C CCDS34946.1 CCDS34946.1 Transcript intron_variant - - - - - - rs6990801 8:141162145 C ENSESTG00000004694 ENSESTT00000011888 Transcript intron_variant - - - - - - rs6990801 8:141162145 C ENSESTG00000004694 ENSESTT00000011896 Transcript intron_variant - - - - - - rs6990801 8:141162145 C 83696 NM_031466.5 Transcript intron_variant - - - - - - rs6990801 8:141162145 C ENSESTG00000004694 ENSESTT00000011911 Transcript intron_variant - - - - - - rs6990801 8:141162145 C ENSESTG00000004694 ENSESTT00000011903 Transcript intron_variant - - - - - - rs6990801 8:141162145 C CCDS55278.1 CCDS55278.1 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009292 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009299 Transcript upstream_gene_variant - - - - - - DISTANCE=923 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009214 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009209 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009288 Transcript downstream_gene_variant - - - - - - DISTANCE=3205 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009105 Transcript intron_variant - - - - - - rs4529507 8:141750131 G CCDS56557.1 CCDS56557.1 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009245 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009256 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009227 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009202 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009231 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009217 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009242 Transcript intron_variant - - - - - - rs4529507 8:141750131 G CCDS6381.1 CCDS6381.1 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009141 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009238 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009182 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009260 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G 5747 NM_153831.3 Transcript intron_variant - - - - - - rs4529507 8:141750131 G 5747 NM_005607.4 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009181 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009261 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009280 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009210 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009282 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009237 Transcript intron_variant - - - - - - rs4529507 8:141750131 G 5747 NM_001199649.1 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009251 Transcript intron_variant - - - - - - rs4529507 8:141750131 G ENSESTG00000003599 ENSESTT00000009206 Transcript downstream_gene_variant - - - - - - DISTANCE=3190 rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009214 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009209 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009105 Transcript intron_variant - - - - - - rs4415367 8:141828763 T CCDS56557.1 CCDS56557.1 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009245 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009256 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009227 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009202 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009231 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009217 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009242 Transcript intron_variant - - - - - - rs4415367 8:141828763 T CCDS6381.1 CCDS6381.1 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009141 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009238 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009182 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009260 Transcript intron_variant - - - - - - rs4415367 8:141828763 T 5747 NM_153831.3 Transcript intron_variant - - - - - - rs4415367 8:141828763 T 5747 NM_005607.4 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009181 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009261 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009210 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009237 Transcript intron_variant - - - - - - rs4415367 8:141828763 T 5747 NM_001199649.1 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009251 Transcript intron_variant - - - - - - rs4415367 8:141828763 T ENSESTG00000003599 ENSESTT00000009206 Transcript intron_variant - - - - - - rs61454150 8:142024903 A - - - intergenic_variant - - - - - - rs7001382 8:142134733 C 22898 NM_014957.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3987 rs7001382 8:142134733 C ENSESTG00000003508 ENSESTT00000008748 Transcript upstream_gene_variant - - - - - - DISTANCE=4008 rs7001382 8:142134733 C ENSESTG00000003508 ENSESTT00000008750 Transcript upstream_gene_variant - - - - - - DISTANCE=4050 rs7009247 8:142290130 C ENSESTG00000003563 ENSESTT00000008886 Transcript intron_variant - - - - - - rs7009247 8:142290130 C ENSESTG00000003565 ENSESTT00000008896 Transcript intron_variant - - - - - - rs9650545 8:142638104 C - - - intergenic_variant - - - - - - rs11167084 8:142709881 C - - - intergenic_variant - - - - - - rs7814656 8:143114905 T - - - intergenic_variant - - - - - - rs10429388 8:143247399 G - - - intergenic_variant - - - - - - rs7837266 8:143319423 C 203062 NM_145003.3 Transcript intron_variant - - - - - - rs7837266 8:143319423 C CCDS6384.1 CCDS6384.1 Transcript intron_variant - - - - - - rs7837266 8:143319423 C ENSESTG00000002521 ENSESTT00000006231 Transcript intron_variant - - - - - - rs7837266 8:143319423 C ENSESTG00000002521 ENSESTT00000006237 Transcript intron_variant - - - - - - rs11777062 8:143352978 G ENSESTG00000002521 ENSESTT00000006244 Transcript missense_variant 294 223 75 T/P Act/Cct - rs11777062 8:143352978 G 203062 NM_145003.3 Transcript intron_variant - - - - - - rs11777062 8:143352978 G CCDS6384.1 CCDS6384.1 Transcript intron_variant - - - - - - rs11777062 8:143352978 G ENSESTG00000002521 ENSESTT00000006231 Transcript intron_variant - - - - - - rs11777062 8:143352978 G ENSESTG00000002521 ENSESTT00000006237 Transcript intron_variant - - - - - - rs13273957 8:143361746 G ENSESTG00000002521 ENSESTT00000006244 Transcript upstream_gene_variant - - - - - - DISTANCE=388 rs13273957 8:143361746 G ENSESTG00000002536 ENSESTT00000006268 Transcript downstream_gene_variant - - - - - - DISTANCE=2888 rs13273957 8:143361746 G ENSESTG00000002536 ENSESTT00000006270 Transcript downstream_gene_variant - - - - - - DISTANCE=2632 rs13273957 8:143361746 G ENSESTG00000002536 ENSESTT00000006273 Transcript downstream_gene_variant - - - - - - DISTANCE=2917 rs13273957 8:143361746 G ENSESTG00000002536 ENSESTT00000006264 Transcript downstream_gene_variant - - - - - - DISTANCE=2250 rs13273957 8:143361746 G ENSESTG00000002521 ENSESTT00000006237 Transcript intron_variant - - - - - - rs13273957 8:143361746 G ENSESTG00000002536 ENSESTT00000006275 Transcript downstream_gene_variant - - - - - - DISTANCE=2511 rs13273957 8:143361746 G ENSESTG00000002536 ENSESTT00000006278 Transcript downstream_gene_variant - - - - - - DISTANCE=2094 rs13273957 8:143361746 G ENSESTG00000002536 ENSESTT00000006272 Transcript downstream_gene_variant - - - - - - DISTANCE=2400 rs13273957 8:143361746 G 203062 NM_145003.3 Transcript intron_variant - - - - - - rs13273957 8:143361746 G ENSESTG00000002536 ENSESTT00000006266 Transcript downstream_gene_variant - - - - - - DISTANCE=2946 rs13273957 8:143361746 G CCDS6384.1 CCDS6384.1 Transcript intron_variant - - - - - - rs13273957 8:143361746 G ENSESTG00000002521 ENSESTT00000006231 Transcript intron_variant - - - - - - rs13273957 8:143361746 G ENSESTG00000002536 ENSESTT00000006283 Transcript downstream_gene_variant - - - - - - DISTANCE=2065 rs6583616 8:143414397 G ENSESTG00000013633 ENSESTT00000034113 Transcript intron_variant - - - - - - rs6583616 8:143414397 G 203062 NM_145003.3 Transcript intron_variant - - - - - - rs6583616 8:143414397 G CCDS6384.1 CCDS6384.1 Transcript intron_variant - - - - - - rs6583616 8:143414397 G ENSESTG00000013633 ENSESTT00000034105 Transcript intron_variant - - - - - - rs6583616 8:143414397 G ENSESTG00000002521 ENSESTT00000006231 Transcript intron_variant - - - - - - rs6583616 8:143414397 G ENSESTG00000013633 ENSESTT00000034111 Transcript intron_variant - - - - - - rs6583641 8:143640284 A - - - intergenic_variant - - - - - - rs9650138 8:143753973 G - ENSR00001446321 RegulatoryFeature regulatory_region_variant - - - - - - rs9650138 8:143753973 G ENSESTG00000013616 ENSESTT00000034059 Transcript downstream_gene_variant - - - - - - DISTANCE=3347 rs9650138 8:143753973 G ENSESTG00000013622 ENSESTT00000034066 Transcript upstream_gene_variant - - - - - - DISTANCE=2572 rs9650138 8:143753973 G ENSESTG00000013616 ENSESTT00000034054 Transcript downstream_gene_variant - - - - - - DISTANCE=3344 rs9650138 8:143753973 G 8000 NR_033343.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs9650138 8:143753973 G 8629 NM_003724.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2572 rs9650138 8:143753973 G ENSESTG00000013455 ENSESTT00000033679 Transcript downstream_gene_variant - - - - - - DISTANCE=2483 rs9650138 8:143753973 G 8629 NM_001077527.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2572 rs7838869 8:143801940 C 100288181 NR_038925.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2585185 8:143830924 G CCDS6388.1 CCDS6388.1 Transcript downstream_gene_variant - - - - - - DISTANCE=777 rs2585185 8:143830924 G ENSESTG00000013605 ENSESTT00000034039 Transcript downstream_gene_variant - - - - - - DISTANCE=644 rs2585185 8:143830924 G 137797 NM_205545.1 Transcript downstream_gene_variant - - - - - - DISTANCE=704 rs2572928 8:143864820 C 8581 NM_003695.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1478 rs2572928 8:143864820 C CCDS6390.1 CCDS6390.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1817 rs2572928 8:143864820 C ENSESTG00000013582 ENSESTT00000033975 Transcript downstream_gene_variant - - - - - - DISTANCE=1494 rs4736355 8:143985563 C ENSESTG00000013481 ENSESTT00000033755 Transcript intron_variant - - - - - - rs11136270 8:144298046 A CCDS34954.1 CCDS34954.1 Transcript downstream_gene_variant - - - - - - DISTANCE=653 rs11136270 8:144298046 A ENSESTG00000013517 ENSESTT00000033845 Transcript downstream_gene_variant - - - - - - DISTANCE=646 rs11136270 8:144298046 A 338328 NM_178172.3 Transcript 3_prime_UTR_variant 1283 - - - - - rs67282719 8:144342142 C 286128 NM_173832.3 Transcript 3_prime_UTR_variant 2053 - - - - - rs67282719 8:144342142 C ENSESTG00000013527 ENSESTT00000033864 Transcript downstream_gene_variant - - - - - - DISTANCE=77 rs2931708 8:144427912 G 116447 NM_001258446.1 Transcript intron_variant - - - - - - rs2931708 8:144427912 G ENSESTG00000011997 ENSESTT00000030060 Transcript intron_variant - - - - - - rs2931708 8:144427912 G 116447 NM_001258447.1 Transcript intron_variant - - - - - - rs2931708 8:144427912 G ENSESTG00000011997 ENSESTT00000030062 Transcript intron_variant - - - - - - rs7000410 8:144758344 C - - - intergenic_variant - - - - - - rs10429438 8:144780670 C ENSESTG00000011415 ENSESTT00000028682 Transcript downstream_gene_variant - - - - - - DISTANCE=4585 rs10429438 8:144780670 C ENSESTG00000011415 ENSESTT00000028675 Transcript downstream_gene_variant - - - - - - DISTANCE=4777 rs10429438 8:144780670 C ENSESTG00000011415 ENSESTT00000028700 Transcript downstream_gene_variant - - - - - - DISTANCE=4797 rs10429438 8:144780670 C 286075 NM_173831.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3115 rs10429438 8:144780670 C 286075 NM_001100598.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3115 rs10429438 8:144780670 C CCDS47932.1 CCDS47932.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3970 rs10429438 8:144780670 C 286075 NM_001100599.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3115 rs10429438 8:144780670 C ENSESTG00000011415 ENSESTT00000028685 Transcript downstream_gene_variant - - - - - - DISTANCE=4752 rs10429438 8:144780670 C 286076 NR_015445.1 Transcript downstream_gene_variant - - - - - - DISTANCE=87 rs6558385 8:144807010 G - ENSR00001404223 RegulatoryFeature regulatory_region_variant - - - - - - rs6558385 8:144807010 G 225689 NM_139021.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2377 rs6558385 8:144807010 G ENSESTG00000011906 ENSESTT00000029807 Transcript downstream_gene_variant - - - - - - DISTANCE=4212 rs6558385 8:144807010 G CCDS6409.2 CCDS6409.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2589 rs6558385 8:144807010 G CCDS6410.2 CCDS6410.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1081 rs6558385 8:144807010 G ENSESTG00000011453 ENSESTT00000028761 Transcript downstream_gene_variant - - - - - - DISTANCE=2384 rs6558385 8:144807010 G ENSESTG00000011453 ENSESTT00000028773 Transcript downstream_gene_variant - - - - - - DISTANCE=2384 rs6558385 8:144807010 G 286077 NM_198488.3 Transcript 3_prime_UTR_variant 4690 - - - - - rs6558385 8:144807010 G ENSESTG00000011453 ENSESTT00000028776 Transcript downstream_gene_variant - - - - - - DISTANCE=2384 rs12676028 8:144814762 G - ENSR00001446390 RegulatoryFeature regulatory_region_variant - - - - - - rs12676028 8:144814762 G 100128338 NR_033849.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1548 rs12676028 8:144814762 G 286077 NM_198488.3 Transcript intron_variant - - - - - - rs12676028 8:144814762 G ENSESTG00000011906 ENSESTT00000029807 Transcript intron_variant - - - - - - rs12676028 8:144814762 G CCDS6410.2 CCDS6410.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2010 rs12676028 8:144814762 G 100616318 NR_039810.1 Transcript downstream_gene_variant - - - - - - DISTANCE=491 rs10098508 8:144890873 T ENSESTG00000011687 ENSESTT00000029284 Transcript intron_variant - - - - - - rs10098508 8:144890873 T 100126338 NR_030633.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4254 rs10098508 8:144890873 T ENSESTG00000011483 ENSESTT00000028805 Transcript downstream_gene_variant - - - - - - DISTANCE=4858 rs10098508 8:144890873 T CCDS6412.1 CCDS6412.1 Transcript missense_variant 2021 2021 674 V/E gTa/gAa - PolyPhen=benign;SIFT=tolerated rs10098508 8:144890873 T 23513 NM_182706.4 Transcript missense_variant 2028 2021 674 V/E gTa/gAa - PolyPhen=benign;SIFT=tolerated rs10098508 8:144890873 T 23513 NM_015356.4 Transcript missense_variant 2028 2021 674 V/E gTa/gAa - PolyPhen=benign;SIFT=tolerated rs10098508 8:144890873 T ENSESTG00000011687 ENSESTT00000029297 Transcript upstream_gene_variant - - - - - - DISTANCE=28 rs10098508 8:144890873 T ENSESTG00000011687 ENSESTT00000029298 Transcript upstream_gene_variant - - - - - - DISTANCE=37 rs10098508 8:144890873 T ENSESTG00000011687 ENSESTT00000029289 Transcript missense_variant 256 128 43 V/E gTa/gAa - rs10098508 8:144890873 T CCDS6411.1 CCDS6411.1 Transcript missense_variant 2021 2021 674 V/E gTa/gAa - PolyPhen=benign;SIFT=tolerated rs6988118 8:145855392 C ENSESTG00000030263 ENSESTT00000076201 Transcript intron_variant - - - - - - rs6988118 8:145855392 C ENSESTG00000029104 ENSESTT00000073271 Transcript upstream_gene_variant - - - - - - DISTANCE=2841 rs6988118 8:145855392 C ENSESTG00000030263 ENSESTT00000076191 Transcript intron_variant - - - - - - rs6988118 8:145855392 C ENSESTG00000030263 ENSESTT00000076132 Transcript intron_variant - - - - - - rs4925837 8:145855592 C ENSESTG00000030263 ENSESTT00000076201 Transcript intron_variant - - - - - - rs4925837 8:145855592 C ENSESTG00000029104 ENSESTT00000073271 Transcript upstream_gene_variant - - - - - - DISTANCE=2641 rs4925837 8:145855592 C ENSESTG00000030263 ENSESTT00000076191 Transcript intron_variant - - - - - - rs4925837 8:145855592 C ENSESTG00000030263 ENSESTT00000076132 Transcript intron_variant - - - - - - rs4582604 8:145859318 A ENSESTG00000030263 ENSESTT00000076201 Transcript intron_variant - - - - - - rs4582604 8:145859318 A ENSESTG00000029104 ENSESTT00000073271 Transcript intron_variant - - - - - - rs4582604 8:145859318 A ENSESTG00000030263 ENSESTT00000076191 Transcript intron_variant - - - - - - rs4582604 8:145859318 A ENSESTG00000030263 ENSESTT00000076132 Transcript intron_variant - - - - - - rs2958503 8:145898523 G ENSESTG00000030263 ENSESTT00000076201 Transcript intron_variant - - - - - - rs2958503 8:145898523 G ENSESTG00000030263 ENSESTT00000076191 Transcript intron_variant - - - - - - rs2958503 8:145898523 G ENSESTG00000030263 ENSESTT00000076132 Transcript intron_variant - - - - - - rs2956189 8:145905694 G ENSESTG00000030263 ENSESTT00000076201 Transcript intron_variant - - - - - - rs2956189 8:145905694 G ENSESTG00000030263 ENSESTT00000076191 Transcript intron_variant - - - - - - rs2956189 8:145905694 G ENSESTG00000030263 ENSESTT00000076132 Transcript intron_variant - - - - - - rs7840641 8:145905827 G ENSESTG00000030263 ENSESTT00000076201 Transcript intron_variant - - - - - - rs7840641 8:145905827 G ENSESTG00000030263 ENSESTT00000076191 Transcript intron_variant - - - - - - rs7840641 8:145905827 G ENSESTG00000030263 ENSESTT00000076132 Transcript intron_variant - - - - - - rs6599534 8:145905850 G ENSESTG00000030263 ENSESTT00000076201 Transcript intron_variant - - - - - - rs6599534 8:145905850 G ENSESTG00000030263 ENSESTT00000076191 Transcript intron_variant - - - - - - rs6599534 8:145905850 G ENSESTG00000030263 ENSESTT00000076132 Transcript intron_variant - - - - - - rs2722492 8:145971396 T ENSESTG00000030214 ENSESTT00000076073 Transcript intron_variant - - - - - - rs2722492 8:145971396 T ENSESTG00000030214 ENSESTT00000076063 Transcript intron_variant - - - - - - rs2722492 8:145971396 T ENSESTG00000030214 ENSESTT00000076081 Transcript intron_variant - - - - - - rs2722492 8:145971396 T CCDS47944.1 CCDS47944.1 Transcript intron_variant - - - - - - rs2722492 8:145971396 T 90987 NM_138367.1 Transcript intron_variant - - - - - - rs2958527 8:146028061 G ENSESTG00000029133 ENSESTT00000073355 Transcript intron_variant - - - - - - rs2958527 8:146028061 G ENSESTG00000029133 ENSESTT00000073393 Transcript intron_variant - - - - - - rs2958527 8:146028061 G ENSESTG00000029133 ENSESTT00000073382 Transcript intron_variant - - - - - - rs2958527 8:146028061 G 340385 NM_213605.2 Transcript intron_variant - - - - - - rs2958527 8:146028061 G ENSESTG00000029133 ENSESTT00000073420 Transcript intron_variant - - - - - - rs2958527 8:146028061 G CCDS6434.1 CCDS6434.1 Transcript upstream_gene_variant - - - - - - DISTANCE=239 rs2958527 8:146028061 G ENSESTG00000029133 ENSESTT00000073403 Transcript intron_variant - - - - - - rs2975281 8:146120966 A - ENSR00001446479 RegulatoryFeature regulatory_region_variant - - - - - - rs2975281 8:146120966 A 58500 NM_001109689.3 Transcript intron_variant - - - - - - rs2975281 8:146120966 A ENSESTG00000029663 ENSESTT00000074629 Transcript intron_variant - - - - - - rs2975281 8:146120966 A 58500 NM_021061.4 Transcript intron_variant - - - - - - rs2975281 8:146120966 A ENSESTG00000029663 ENSESTT00000074739 Transcript intron_variant - - - - - - rs2975281 8:146120966 A ENSESTG00000029663 ENSESTT00000074772 Transcript intron_variant - - - - - - rs2975281 8:146120966 A ENSESTG00000029663 ENSESTT00000074645 Transcript intron_variant - - - - - - rs2975281 8:146120966 A ENSESTG00000029663 ENSESTT00000074754 Transcript intron_variant - - - - - - rs2975281 8:146120966 A ENSESTG00000029663 ENSESTT00000074721 Transcript intron_variant - - - - - - rs2975281 8:146120966 A ENSESTG00000029663 ENSESTT00000074706 Transcript intron_variant - - - - - - rs2956167 8:146162446 C CCDS6437.1 CCDS6437.1 Transcript intron_variant - - - - - - rs2956167 8:146162446 C ENSESTG00000029612 ENSESTT00000074572 Transcript intron_variant - - - - - - rs2956167 8:146162446 C ENSESTG00000029612 ENSESTT00000074557 Transcript intron_variant - - - - - - rs2956167 8:146162446 C ENSESTG00000029612 ENSESTT00000074583 Transcript intron_variant - - - - - - rs2956167 8:146162446 C 7564 NM_001029976.2 Transcript intron_variant - - - - - - rs2956167 8:146162446 C 7564 NM_006958.2 Transcript intron_variant - - - - - - rs2978409 8:146221823 T ENSESTG00000029558 ENSESTT00000074352 Transcript downstream_gene_variant - - - - - - DISTANCE=1218 rs2978409 8:146221823 T 286101 NR_023392.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2978409 8:146221823 T ENSESTG00000029590 ENSESTT00000074462 Transcript intron_variant - - - - - - rs2978409 8:146221823 T 286102 NR_002807.3 Transcript non_coding_exon_variant,nc_transcript_variant 1573 - - - - - rs2978409 8:146221823 T ENSESTG00000029590 ENSESTT00000074494 Transcript intron_variant - - - - - - rs13266446 8:146266998 T - - - intergenic_variant - - - - - - rs6477065 9:638711 T ENSESTG00000022871 ENSESTT00000057895 Transcript intron_variant - - - - - - rs6477065 9:638711 T ENSESTG00000022871 ENSESTT00000057874 Transcript intron_variant - - - - - - rs6477065 9:638711 T ENSESTG00000022871 ENSESTT00000057681 Transcript intron_variant - - - - - - rs6477065 9:638711 T ENSESTG00000022871 ENSESTT00000057953 Transcript intron_variant - - - - - - rs6477065 9:638711 T 23189 NM_015158.3 Transcript intron_variant - - - - - - rs6477065 9:638711 T 23189 NM_001256877.1 Transcript intron_variant - - - - - - rs6477065 9:638711 T 23189 NM_001256876.1 Transcript intron_variant - - - - - - rs6477065 9:638711 T ENSESTG00000022871 ENSESTT00000057973 Transcript upstream_gene_variant - - - - - - DISTANCE=4161 rs2185362 9:1341233 A - - - intergenic_variant - - - - - - rs771900 9:1650686 G - - - intergenic_variant - - - - - - rs4741610 9:1819327 C - - - intergenic_variant - - - - - - rs1411908 9:1850864 T - - - intergenic_variant - - - - - - rs6475660 9:2265003 C - - - intergenic_variant - - - - - - rs7856697 9:2271862 C - ENSR00001299064 RegulatoryFeature regulatory_region_variant - - - - - - rs7856697 9:2271862 C - - - intergenic_variant - - - - - - rs1154630 9:2423359 G - - - intergenic_variant - - - - - - rs513148 9:2578275 A 401491 NR_015375.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs513148 9:2578275 A ENSESTG00000007076 ENSESTT00000017907 Transcript intron_variant - - - - - - rs1889110 9:2800383 T CCDS6448.2 CCDS6448.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3948 rs1889110 9:2800383 T 9933 NM_014878.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3769 rs1889110 9:2800383 T ENSESTG00000007021 ENSESTT00000017887 Transcript downstream_gene_variant - - - - - - DISTANCE=4030 rs3847249 9:3061750 G ENSESTG00000001148 ENSESTT00000002730 Transcript intron_variant - - - - - - rs3847251 9:3061829 A ENSESTG00000001148 ENSESTT00000002730 Transcript intron_variant - - - - - - rs4741804 9:3062214 G ENSESTG00000001148 ENSESTT00000002730 Transcript intron_variant - - - - - - rs4741810 9:3179618 T ENSESTG00000001148 ENSESTT00000002730 Transcript intron_variant - - - - - - rs10758508 9:3869520 A 169792 NM_152629.3 Transcript intron_variant - - - - - - rs10758508 9:3869520 A 169792 NM_001042413.1 Transcript intron_variant - - - - - - rs10758508 9:3869520 A CCDS43784.1 CCDS43784.1 Transcript intron_variant - - - - - - rs10758508 9:3869520 A CCDS6451.1 CCDS6451.1 Transcript intron_variant - - - - - - rs10758508 9:3869520 A ENSESTG00000001095 ENSESTT00000002617 Transcript intron_variant - - - - - - rs508122 9:3992497 C 169792 NM_152629.3 Transcript intron_variant - - - - - - rs508122 9:3992497 C 169792 NM_001042413.1 Transcript intron_variant - - - - - - rs508122 9:3992497 C CCDS43784.1 CCDS43784.1 Transcript intron_variant - - - - - - rs508122 9:3992497 C CCDS6451.1 CCDS6451.1 Transcript intron_variant - - - - - - rs508122 9:3992497 C ENSESTG00000001105 ENSESTT00000002634 Transcript intron_variant - - - - - - rs663822 9:3995219 C 169792 NM_152629.3 Transcript intron_variant - - - - - - rs663822 9:3995219 C 169792 NM_001042413.1 Transcript intron_variant - - - - - - rs663822 9:3995219 C CCDS43784.1 CCDS43784.1 Transcript intron_variant - - - - - - rs663822 9:3995219 C CCDS6451.1 CCDS6451.1 Transcript intron_variant - - - - - - rs663822 9:3995219 C ENSESTG00000001105 ENSESTT00000002634 Transcript intron_variant - - - - - - rs2755088 9:4090747 G - ENSR00001299283 RegulatoryFeature regulatory_region_variant - - - - - - rs2755088 9:4090747 G 169792 NM_152629.3 Transcript intron_variant - - - - - - rs2755088 9:4090747 G 169792 NM_001042413.1 Transcript intron_variant - - - - - - rs2755088 9:4090747 G CCDS43784.1 CCDS43784.1 Transcript intron_variant - - - - - - rs2755088 9:4090747 G CCDS6451.1 CCDS6451.1 Transcript intron_variant - - - - - - rs2380939 9:4146694 C 169792 NM_152629.3 Transcript intron_variant - - - - - - rs2380939 9:4146694 C 169792 NM_001042413.1 Transcript intron_variant - - - - - - rs2380939 9:4146694 C CCDS43784.1 CCDS43784.1 Transcript intron_variant - - - - - - rs2380939 9:4146694 C ENSESTG00000003246 ENSESTT00000008067 Transcript intron_variant - - - - - - rs2380939 9:4146694 C ENSESTG00000003246 ENSESTT00000008064 Transcript intron_variant - - - - - - rs6476820 9:4191582 A 169792 NM_001042413.1 Transcript intron_variant - - - - - - rs6476820 9:4191582 A CCDS43784.1 CCDS43784.1 Transcript intron_variant - - - - - - rs6476820 9:4191582 A ENSESTG00000003246 ENSESTT00000008064 Transcript intron_variant - - - - - - rs4237149 9:4271568 A 169792 NM_001042413.1 Transcript intron_variant - - - - - - rs4237149 9:4271568 A CCDS43784.1 CCDS43784.1 Transcript intron_variant - - - - - - rs4237149 9:4271568 A ENSESTG00000003246 ENSESTT00000008064 Transcript intron_variant - - - - - - rs6476843 9:4291407 T 169792 NM_001042413.1 Transcript intron_variant - - - - - - rs6476843 9:4291407 T CCDS43784.1 CCDS43784.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4982 rs6476843 9:4291407 T ENSESTG00000003246 ENSESTT00000008064 Transcript intron_variant - - - - - - rs10758599 9:4306047 A - - - intergenic_variant - - - - - - rs1888209 9:4317589 A - - - intergenic_variant - - - - - - rs1023110 9:4317772 T - - - intergenic_variant - - - - - - rs4741970 9:4377748 G - - - intergenic_variant - - - - - - rs301452 9:4604702 C - ENSR00001299378 RegulatoryFeature regulatory_region_variant - - - - - - rs301452 9:4604702 C CCDS43785.2 CCDS43785.2 Transcript intron_variant - - - - - - rs301452 9:4604702 C ENSESTG00000003223 ENSESTT00000008053 Transcript intron_variant - - - - - - rs301452 9:4604702 C ENSESTG00000003223 ENSESTT00000008056 Transcript intron_variant - - - - - - rs301452 9:4604702 C 55064 NM_001039395.3 Transcript intron_variant - - - - - - rs687073 9:4693791 A ENSESTG00000003167 ENSESTT00000007894 Transcript intron_variant - - - - - - rs687073 9:4693791 A 55664 NM_017913.2 Transcript intron_variant - - - - - - rs687073 9:4693791 A CCDS6454.1 CCDS6454.1 Transcript intron_variant - - - - - - rs296838 9:4804950 C ENSESTG00000003190 ENSESTT00000007953 Transcript intron_variant - - - - - - rs296838 9:4804950 C ENSESTG00000003190 ENSESTT00000007949 Transcript intron_variant - - - - - - rs296838 9:4804950 C 10171 NM_005772.3 Transcript intron_variant - - - - - - rs296838 9:4804950 C CCDS6456.1 CCDS6456.1 Transcript intron_variant - - - - - - rs1473731 9:5276151 G - - - intergenic_variant - - - - - - rs10739072 9:5295489 C CCDS6460.1 CCDS6460.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4609 rs10739072 9:5295489 C 6019 NM_134441.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4379 rs10739072 9:5295489 C 6019 NM_005059.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4379 rs1329945 9:5456775 G 29126 NM_001267706.1 Transcript intron_variant - - - - - - rs1329945 9:5456775 G 29126 NR_052005.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1329945 9:5456775 G ENSESTG00000011104 ENSESTT00000027897 Transcript intron_variant - - - - - - rs1329945 9:5456775 G CCDS59118.1 CCDS59118.1 Transcript intron_variant - - - - - - rs1329945 9:5456775 G CCDS6464.1 CCDS6464.1 Transcript intron_variant - - - - - - rs1329945 9:5456775 G ENSESTG00000010970 ENSESTT00000027489 Transcript intron_variant - - - - - - rs1329945 9:5456775 G 29126 NM_014143.3 Transcript intron_variant - - - - - - rs10815240 9:5507821 C 80380 NM_025239.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2724 rs10815240 9:5507821 C ENSESTG00000010979 ENSESTT00000027506 Transcript upstream_gene_variant - - - - - - DISTANCE=2706 rs10815240 9:5507821 C ENSESTG00000011104 ENSESTT00000027897 Transcript intron_variant - - - - - - rs4143814 9:5588798 G ENSESTG00000011104 ENSESTT00000027897 Transcript intron_variant - - - - - - rs4143814 9:5588798 G ENSESTG00000011104 ENSESTT00000027864 Transcript intron_variant - - - - - - rs995919 9:6253186 G ENSESTG00000004753 ENSESTT00000012029 Transcript downstream_gene_variant - - - - - - DISTANCE=192 rs995919 9:6253186 G 90865 NM_033439.3 Transcript intron_variant - - - - - - rs995919 9:6253186 G 90865 NM_001199641.1 Transcript intron_variant - - - - - - rs995919 9:6253186 G ENSESTG00000004753 ENSESTT00000012040 Transcript intron_variant - - - - - - rs995919 9:6253186 G ENSESTG00000004753 ENSESTT00000012047 Transcript intron_variant - - - - - - rs995919 9:6253186 G ENSESTG00000004753 ENSESTT00000012044 Transcript intron_variant - - - - - - rs995919 9:6253186 G ENSESTG00000004753 ENSESTT00000012037 Transcript intron_variant - - - - - - rs995919 9:6253186 G CCDS56564.1 CCDS56564.1 Transcript intron_variant - - - - - - rs995919 9:6253186 G 90865 NM_001199640.1 Transcript intron_variant - - - - - - rs995919 9:6253186 G CCDS56563.1 CCDS56563.1 Transcript intron_variant - - - - - - rs995919 9:6253186 G ENSESTG00000004753 ENSESTT00000012045 Transcript intron_variant - - - - - - rs995919 9:6253186 G CCDS6468.1 CCDS6468.1 Transcript intron_variant - - - - - - rs946923 9:6932266 G - ENSR00001469047 RegulatoryFeature regulatory_region_variant - - - - - - rs946923 9:6932266 G ENSESTG00000004850 ENSESTT00000012297 Transcript intron_variant - - - - - - rs946923 9:6932266 G CCDS55285.1 CCDS55285.1 Transcript intron_variant - - - - - - rs946923 9:6932266 G 23081 NM_001146694.1 Transcript intron_variant - - - - - - rs946923 9:6932266 G CCDS55286.1 CCDS55286.1 Transcript intron_variant - - - - - - rs946923 9:6932266 G 23081 NM_015061.3 Transcript intron_variant - - - - - - rs946923 9:6932266 G CCDS6471.1 CCDS6471.1 Transcript intron_variant - - - - - - rs946923 9:6932266 G ENSESTG00000004819 ENSESTT00000012275 Transcript intron_variant - - - - - - rs946923 9:6932266 G 23081 NM_001146695.1 Transcript intron_variant - - - - - - rs946923 9:6932266 G 23081 NM_001146696.1 Transcript intron_variant - - - - - - rs946923 9:6932266 G ENSESTG00000004819 ENSESTT00000012286 Transcript intron_variant - - - - - - rs946923 9:6932266 G CCDS55287.1 CCDS55287.1 Transcript intron_variant - - - - - - rs818904 9:6987111 C 23081 NM_001146694.1 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000013526 ENSESTT00000033937 Transcript intron_variant - - - - - - rs818904 9:6987111 C CCDS55286.1 CCDS55286.1 Transcript intron_variant - - - - - - rs818904 9:6987111 C 23081 NM_015061.3 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000013526 ENSESTT00000033953 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000004819 ENSESTT00000012275 Transcript downstream_gene_variant - - - - - - DISTANCE=733 rs818904 9:6987111 C ENSESTG00000013526 ENSESTT00000033944 Transcript intron_variant - - - - - - rs818904 9:6987111 C 23081 NM_001146696.1 Transcript intron_variant - - - - - - rs818904 9:6987111 C CCDS55287.1 CCDS55287.1 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000013526 ENSESTT00000033958 Transcript downstream_gene_variant - - - - - - DISTANCE=290 rs818904 9:6987111 C CCDS55285.1 CCDS55285.1 Transcript intron_variant - - - - - - rs818904 9:6987111 C CCDS6471.1 CCDS6471.1 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000013526 ENSESTT00000033949 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000013526 ENSESTT00000033928 Transcript intron_variant - - - - - - rs818904 9:6987111 C 23081 NM_001146695.1 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000013526 ENSESTT00000033939 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000013526 ENSESTT00000033936 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000013526 ENSESTT00000033950 Transcript intron_variant - - - - - - rs818904 9:6987111 C ENSESTG00000004819 ENSESTT00000012286 Transcript downstream_gene_variant - - - - - - DISTANCE=2748 rs1323403 9:7081810 A 23081 NM_001146694.1 Transcript intron_variant - - - - - - rs1323403 9:7081810 A ENSESTG00000013526 ENSESTT00000033937 Transcript intron_variant - - - - - - rs1323403 9:7081810 A 23081 NM_015061.3 Transcript intron_variant - - - - - - rs1323403 9:7081810 A ENSESTG00000013526 ENSESTT00000033949 Transcript intron_variant - - - - - - rs1323403 9:7081810 A CCDS6471.1 CCDS6471.1 Transcript intron_variant - - - - - - rs1323403 9:7081810 A ENSESTG00000013526 ENSESTT00000033928 Transcript intron_variant - - - - - - rs1323403 9:7081810 A ENSESTG00000013526 ENSESTT00000033944 Transcript intron_variant - - - - - - rs1323403 9:7081810 A ENSESTG00000013526 ENSESTT00000033939 Transcript intron_variant - - - - - - rs1323403 9:7081810 A 23081 NM_001146695.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4546 rs1323403 9:7081810 A ENSESTG00000013526 ENSESTT00000033936 Transcript intron_variant - - - - - - rs1323403 9:7081810 A ENSESTG00000013526 ENSESTT00000033950 Transcript intron_variant - - - - - - rs1323403 9:7081810 A 23081 NM_001146696.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4546 rs1323403 9:7081810 A CCDS55287.1 CCDS55287.1 Transcript intron_variant - - - - - - rs2820948 9:7266570 C - - - intergenic_variant - - - - - - rs62529955 9:7401895 A ENSESTG00000013579 ENSESTT00000033974 Transcript downstream_gene_variant - - - - - - DISTANCE=3325 rs2997571 9:7407211 G - - - intergenic_variant - - - - - - rs2381606 9:7455568 A - - - intergenic_variant - - - - - - rs7864541 9:7553563 G - - - intergenic_variant - - - - - - rs2381677 9:7903464 C - - - intergenic_variant - - - - - - rs1121437 9:8049721 G - - - intergenic_variant - - - - - - rs7037004 9:8686407 C CCDS55289.1 CCDS55289.1 Transcript intron_variant - - - - - - rs7037004 9:8686407 C 5789 NM_130391.3 Transcript intron_variant - - - - - - rs7037004 9:8686407 C CCDS43786.1 CCDS43786.1 Transcript intron_variant - - - - - - rs7037004 9:8686407 C 5789 NM_001171025.1 Transcript intron_variant - - - - - - rs7037004 9:8686407 C ENSESTG00000021895 ENSESTT00000055126 Transcript intron_variant - - - - - - rs7037004 9:8686407 C 5789 NM_130392.3 Transcript intron_variant - - - - - - rs7037004 9:8686407 C 5789 NM_002839.3 Transcript intron_variant - - - - - - rs7037004 9:8686407 C CCDS6472.2 CCDS6472.2 Transcript intron_variant - - - - - - rs7037004 9:8686407 C 5789 NM_130393.3 Transcript intron_variant - - - - - - rs7037004 9:8686407 C CCDS55288.1 CCDS55288.1 Transcript intron_variant - - - - - - rs7037004 9:8686407 C CCDS55290.1 CCDS55290.1 Transcript intron_variant - - - - - - rs7037004 9:8686407 C 5789 NM_001040712.2 Transcript intron_variant - - - - - - rs1897673 9:8901452 T 5789 NM_002839.3 Transcript intron_variant - - - - - - rs1897672 9:8901645 T 5789 NM_002839.3 Transcript intron_variant - - - - - - rs4256637 9:8944965 C 5789 NM_002839.3 Transcript intron_variant - - - - - - rs1992673 9:9145663 T 5789 NM_002839.3 Transcript intron_variant - - - - - - rs2802279 9:9315712 T - ENSR00001299972 RegulatoryFeature regulatory_region_variant - - - - - - rs2802279 9:9315712 T 5789 NM_002839.3 Transcript intron_variant - - - - - - rs7852765 9:9719917 C ENSESTG00000023826 ENSESTT00000060049 Transcript intron_variant - - - - - - rs7852765 9:9719917 C 5789 NM_002839.3 Transcript intron_variant - - - - - - rs2821514 9:9762355 C ENSESTG00000023826 ENSESTT00000060049 Transcript intron_variant - - - - - - rs2821514 9:9762355 C 5789 NM_002839.3 Transcript intron_variant - - - - - - rs1323792 9:9854837 T ENSESTG00000023826 ENSESTT00000060049 Transcript intron_variant - - - - - - rs1323792 9:9854837 T 5789 NM_002839.3 Transcript intron_variant - - - - - - rs942160 9:10292266 T 5789 NM_002839.3 Transcript intron_variant - - - - - - rs663047 9:10299531 G 5789 NM_002839.3 Transcript intron_variant - - - - - - rs942161 9:10332474 G 5789 NM_002839.3 Transcript intron_variant - - - - - - rs1535662 9:10350034 G 5789 NM_002839.3 Transcript intron_variant - - - - - - rs7853671 9:10380427 A 5789 NM_002839.3 Transcript intron_variant - - - - - - rs7858197 9:10698814 A - - - intergenic_variant - - - - - - rs7861022 9:10699059 G - - - intergenic_variant - - - - - - rs10733237 9:11898544 A - - - intergenic_variant - - - - - - rs791776 9:12146653 T - - - intergenic_variant - - - - - - rs791778 9:12158422 C - - - intergenic_variant - - - - - - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049496 Transcript synonymous_variant 2026 1317 439 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049560 Transcript intron_variant - - - - - - rs10809904 9:13112116 G 8777 NM_001261406.1 Transcript synonymous_variant 5754 5532 1844 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049551 Transcript intron_variant - - - - - - rs10809904 9:13112116 G CCDS59120.1 CCDS59120.1 Transcript synonymous_variant 5532 5532 1844 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049537 Transcript synonymous_variant 1972 1263 421 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049478 Transcript synonymous_variant 2118 1710 570 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049679 Transcript synonymous_variant 2121 1263 421 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049674 Transcript synonymous_variant 2213 2043 681 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049525 Transcript synonymous_variant 2064 1656 552 I atT/atC - rs10809904 9:13112116 G 8777 NM_003829.4 Transcript synonymous_variant 5766 5544 1848 I atT/atC - rs10809904 9:13112116 G CCDS59119.1 CCDS59119.1 Transcript synonymous_variant 5445 5445 1815 I atT/atC - rs10809904 9:13112116 G CCDS47951.1 CCDS47951.1 Transcript synonymous_variant 5544 5544 1848 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049667 Transcript synonymous_variant 2175 1317 439 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049684 Transcript intron_variant - - - - - - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049689 Transcript intron_variant - - - - - - rs10809904 9:13112116 G 8777 NM_001261407.1 Transcript synonymous_variant 5667 5445 1815 I atT/atC - rs10809904 9:13112116 G ENSESTG00000019628 ENSESTT00000049635 Transcript synonymous_variant 2267 2097 699 I atT/atC - rs1147776 9:13260614 C 8777 NM_003829.4 Transcript intron_variant - - - - - - rs1147776 9:13260614 C 8777 NM_001261406.1 Transcript intron_variant - - - - - - rs1147776 9:13260614 C 8777 NM_001261407.1 Transcript intron_variant - - - - - - rs2841174 9:13369795 C - - - intergenic_variant - - - - - - rs2841175 9:13381002 G - - - intergenic_variant - - - - - - rs6474782 9:13554491 C - - - intergenic_variant - - - - - - rs513958 9:14090333 C CCDS55292.1 CCDS55292.1 Transcript intron_variant - - - - - - rs513958 9:14090333 C 4781 NM_001190737.1 Transcript intron_variant - - - - - - rs513958 9:14090333 C ENSESTG00000003777 ENSESTT00000009570 Transcript intron_variant - - - - - - rs513958 9:14090333 C 4781 NM_001190738.1 Transcript intron_variant - - - - - - rs513958 9:14090333 C ENSESTG00000003777 ENSESTT00000009541 Transcript intron_variant - - - - - - rs513958 9:14090333 C ENSESTG00000003777 ENSESTT00000009538 Transcript intron_variant - - - - - - rs513958 9:14090333 C 4781 NM_005596.3 Transcript intron_variant - - - - - - rs513958 9:14090333 C ENSESTG00000003777 ENSESTT00000009549 Transcript intron_variant - - - - - - rs513958 9:14090333 C ENSESTG00000003777 ENSESTT00000009562 Transcript intron_variant - - - - - - rs513958 9:14090333 C CCDS6474.1 CCDS6474.1 Transcript intron_variant - - - - - - rs513958 9:14090333 C CCDS55291.1 CCDS55291.1 Transcript intron_variant - - - - - - rs513958 9:14090333 C ENSESTG00000003777 ENSESTT00000009566 Transcript intron_variant - - - - - - rs513958 9:14090333 C ENSESTG00000003777 ENSESTT00000009559 Transcript intron_variant - - - - - - rs513958 9:14090333 C ENSESTG00000003777 ENSESTT00000009553 Transcript intron_variant - - - - - - rs9407573 9:14513509 C - - - intergenic_variant - - - - - - rs3119698 9:15634193 A CCDS6481.1 CCDS6481.1 Transcript intron_variant - - - - - - rs3119698 9:15634193 A 203238 NM_173550.2 Transcript intron_variant - - - - - - rs1935222 9:15787691 A CCDS6481.1 CCDS6481.1 Transcript intron_variant - - - - - - rs1935222 9:15787691 A ENSESTG00000034227 ENSESTT00000086554 Transcript intron_variant - - - - - - rs1935222 9:15787691 A ENSESTG00000034227 ENSESTT00000086545 Transcript intron_variant - - - - - - rs1935222 9:15787691 A 203238 NM_173550.2 Transcript intron_variant - - - - - - rs1935222 9:15787691 A ENSESTG00000034227 ENSESTT00000086560 Transcript intron_variant - - - - - - rs3008711 9:16018178 A - - - intergenic_variant - - - - - - rs1927703 9:16109291 G - - - intergenic_variant - - - - - - rs1927627 9:16417431 A - ENSR00001469489 RegulatoryFeature regulatory_region_variant - - - - - - rs1927627 9:16417431 A CCDS6482.2 CCDS6482.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1556 rs1927627 9:16417431 A ENSESTG00000001378 ENSESTT00000003251 Transcript upstream_gene_variant - - - - - - DISTANCE=697 rs1927627 9:16417431 A 54796 NM_017637.5 Transcript 3_prime_UTR_variant 4996 - - - - - rs10115468 9:16549659 A CCDS6482.2 CCDS6482.2 Transcript intron_variant - - - - - - rs10115468 9:16549659 A ENSESTG00000001393 ENSESTT00000003274 Transcript downstream_gene_variant - - - - - - DISTANCE=3004 rs10115468 9:16549659 A ENSESTG00000001393 ENSESTT00000003286 Transcript intron_variant - - - - - - rs10115468 9:16549659 A 54796 NM_017637.5 Transcript intron_variant - - - - - - rs10115468 9:16549659 A ENSESTG00000001393 ENSESTT00000003278 Transcript downstream_gene_variant - - - - - - DISTANCE=2939 rs10115468 9:16549659 A ENSESTG00000001393 ENSESTT00000003294 Transcript intron_variant - - - - - - rs9406648 9:16585904 G CCDS6482.2 CCDS6482.2 Transcript intron_variant - - - - - - rs9406648 9:16585904 G ENSESTG00000001393 ENSESTT00000003274 Transcript intron_variant - - - - - - rs9406648 9:16585904 G ENSESTG00000001393 ENSESTT00000003286 Transcript intron_variant - - - - - - rs9406648 9:16585904 G 54796 NM_017637.5 Transcript intron_variant - - - - - - rs9406648 9:16585904 G ENSESTG00000001393 ENSESTT00000003271 Transcript intron_variant - - - - - - rs9406648 9:16585904 G ENSESTG00000001393 ENSESTT00000003278 Transcript intron_variant - - - - - - rs9406648 9:16585904 G ENSESTG00000001393 ENSESTT00000003276 Transcript intron_variant - - - - - - rs945800 9:16637278 G - ENSR00001300677 RegulatoryFeature regulatory_region_variant - - - - - - rs945800 9:16637278 G CCDS6482.2 CCDS6482.2 Transcript intron_variant - - - - - - rs945800 9:16637278 G ENSESTG00000001393 ENSESTT00000003274 Transcript intron_variant - - - - - - rs945800 9:16637278 G ENSESTG00000001393 ENSESTT00000003286 Transcript intron_variant - - - - - - rs945800 9:16637278 G 54796 NM_017637.5 Transcript intron_variant - - - - - - rs945800 9:16637278 G ENSESTG00000001393 ENSESTT00000003271 Transcript intron_variant - - - - - - rs945800 9:16637278 G ENSESTG00000001393 ENSESTT00000003278 Transcript intron_variant - - - - - - rs945800 9:16637278 G ENSESTG00000001393 ENSESTT00000003276 Transcript intron_variant - - - - - - rs7020450 9:16653027 G - ENSR00001300681 RegulatoryFeature regulatory_region_variant - - - - - - rs7020450 9:16653027 G CCDS6482.2 CCDS6482.2 Transcript intron_variant - - - - - - rs7020450 9:16653027 G ENSESTG00000001393 ENSESTT00000003274 Transcript intron_variant - - - - - - rs7020450 9:16653027 G ENSESTG00000001393 ENSESTT00000003286 Transcript intron_variant - - - - - - rs7020450 9:16653027 G 54796 NM_017637.5 Transcript intron_variant - - - - - - rs7020450 9:16653027 G ENSESTG00000001393 ENSESTT00000003271 Transcript intron_variant - - - - - - rs7020450 9:16653027 G ENSESTG00000001393 ENSESTT00000003278 Transcript intron_variant - - - - - - rs7020450 9:16653027 G ENSESTG00000001393 ENSESTT00000003276 Transcript intron_variant - - - - - - rs4378057 9:16826143 T - ENSR00001300709 RegulatoryFeature regulatory_region_variant - - - - - - rs4378057 9:16826143 T CCDS6482.2 CCDS6482.2 Transcript intron_variant - - - - - - rs4378057 9:16826143 T ENSESTG00000001393 ENSESTT00000003274 Transcript intron_variant - - - - - - rs4378057 9:16826143 T 54796 NM_017637.5 Transcript intron_variant - - - - - - rs4378057 9:16826143 T ENSESTG00000001393 ENSESTT00000003271 Transcript intron_variant - - - - - - rs4378057 9:16826143 T ENSESTG00000001393 ENSESTT00000003276 Transcript intron_variant - - - - - - rs444634 9:17130758 T CCDS47953.1 CCDS47953.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4306 rs444634 9:17130758 T CCDS43789.1 CCDS43789.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4306 rs444634 9:17130758 T 54875 NM_017738.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4280 rs444634 9:17130758 T 54875 NM_001114395.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4280 rs2593399 9:17465746 T CCDS43789.1 CCDS43789.1 Transcript intron_variant - - - - - - rs2593399 9:17465746 T 54875 NM_017738.2 Transcript intron_variant - - - - - - rs4961574 9:17579198 G - ENSR00001300787 RegulatoryFeature regulatory_region_variant - - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039799 Transcript 5_prime_UTR_variant 15 - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039695 Transcript 5_prime_UTR_variant 78 - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039760 Transcript 5_prime_UTR_variant 76 - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039700 Transcript 5_prime_UTR_variant 78 - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039735 Transcript 5_prime_UTR_variant 78 - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039727 Transcript 5_prime_UTR_variant 78 - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039748 Transcript 5_prime_UTR_variant 77 - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039687 Transcript 5_prime_UTR_variant 78 - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039674 Transcript 5_prime_UTR_variant 120 - - - - - rs4961574 9:17579198 G CCDS6483.1 CCDS6483.1 Transcript upstream_gene_variant - - - - - - DISTANCE=43 rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039803 Transcript upstream_gene_variant - - - - - - DISTANCE=1241 rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039716 Transcript 5_prime_UTR_variant 78 - - - - - rs4961574 9:17579198 G 6456 NM_003026.2 Transcript 5_prime_UTR_variant 246 - - - - - rs4961574 9:17579198 G ENSESTG00000015810 ENSESTT00000039635 Transcript 5_prime_UTR_variant 246 - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039799 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039695 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039760 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039700 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039735 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039727 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039748 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039687 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039674 Transcript intron_variant - - - - - - rs7875694 9:17594659 A CCDS6483.1 CCDS6483.1 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039803 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039716 Transcript intron_variant - - - - - - rs7875694 9:17594659 A 6456 NM_003026.2 Transcript intron_variant - - - - - - rs7875694 9:17594659 A ENSESTG00000015810 ENSESTT00000039635 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039799 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039695 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039760 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039700 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039735 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039727 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039748 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039687 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039674 Transcript intron_variant - - - - - - rs2147734 9:17716342 T CCDS6483.1 CCDS6483.1 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039803 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039716 Transcript intron_variant - - - - - - rs2147734 9:17716342 T 6456 NM_003026.2 Transcript intron_variant - - - - - - rs2147734 9:17716342 T ENSESTG00000015810 ENSESTT00000039635 Transcript intron_variant - - - - - - rs9407885 9:17796948 C ENSESTG00000015810 ENSESTT00000039695 Transcript downstream_gene_variant - - - - - - DISTANCE=661 rs9407885 9:17796948 C ENSESTG00000015810 ENSESTT00000039700 Transcript downstream_gene_variant - - - - - - DISTANCE=864 rs9407885 9:17796948 C ENSESTG00000015810 ENSESTT00000039727 Transcript downstream_gene_variant - - - - - - DISTANCE=3504 rs9407885 9:17796948 C ENSESTG00000015810 ENSESTT00000039687 Transcript downstream_gene_variant - - - - - - DISTANCE=618 rs9407885 9:17796948 C CCDS6483.1 CCDS6483.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1207 rs9407885 9:17796948 C ENSESTG00000015810 ENSESTT00000039716 Transcript downstream_gene_variant - - - - - - DISTANCE=1319 rs9407885 9:17796948 C 6456 NM_003026.2 Transcript 3_prime_UTR_variant 2554 - - - - - rs9407885 9:17796948 C ENSESTG00000015810 ENSESTT00000039635 Transcript downstream_gene_variant - - - - - - DISTANCE=3529 rs7042223 9:17797260 G ENSESTG00000015810 ENSESTT00000039695 Transcript downstream_gene_variant - - - - - - DISTANCE=973 rs7042223 9:17797260 G ENSESTG00000015810 ENSESTT00000039700 Transcript downstream_gene_variant - - - - - - DISTANCE=1176 rs7042223 9:17797260 G ENSESTG00000015810 ENSESTT00000039727 Transcript downstream_gene_variant - - - - - - DISTANCE=3816 rs7042223 9:17797260 G ENSESTG00000015810 ENSESTT00000039687 Transcript downstream_gene_variant - - - - - - DISTANCE=930 rs7042223 9:17797260 G CCDS6483.1 CCDS6483.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1519 rs7042223 9:17797260 G ENSESTG00000015810 ENSESTT00000039716 Transcript downstream_gene_variant - - - - - - DISTANCE=1631 rs7042223 9:17797260 G 6456 NM_003026.2 Transcript downstream_gene_variant - - - - - - DISTANCE=138 rs7042223 9:17797260 G ENSESTG00000015810 ENSESTT00000039635 Transcript downstream_gene_variant - - - - - - DISTANCE=3841 rs4341244 9:17907330 G - - - intergenic_variant - - - - - - rs6475192 9:17946019 A - - - intergenic_variant - - - - - - rs492055 9:18068581 C - - - intergenic_variant - - - - - - rs536651 9:18093946 G - - - intergenic_variant - - - - - - rs7026054 9:18235579 G - - - intergenic_variant - - - - - - rs2791451 9:18409783 G ENSESTG00000015634 ENSESTT00000039150 Transcript intron_variant - - - - - - rs934481 9:18891513 A ENSESTG00000015713 ENSESTT00000039334 Transcript downstream_gene_variant - - - - - - DISTANCE=726 rs934481 9:18891513 A ENSESTG00000015713 ENSESTT00000039332 Transcript intron_variant - - - - - - rs934481 9:18891513 A 92949 NM_001040272.5 Transcript intron_variant - - - - - - rs934481 9:18891513 A CCDS47954.1 CCDS47954.1 Transcript intron_variant - - - - - - rs10757045 9:19275390 A ENSESTG00000032696 ENSESTT00000082829 Transcript upstream_gene_variant - - - - - - DISTANCE=1060 rs10757045 9:19275390 A ENSESTG00000032696 ENSESTT00000082820 Transcript upstream_gene_variant - - - - - - DISTANCE=1060 rs10757045 9:19275390 A ENSESTG00000032696 ENSESTT00000082815 Transcript upstream_gene_variant - - - - - - DISTANCE=1060 rs10757045 9:19275390 A ENSESTG00000032696 ENSESTT00000082753 Transcript upstream_gene_variant - - - - - - DISTANCE=1060 rs10757045 9:19275390 A ENSESTG00000032696 ENSESTT00000082586 Transcript intron_variant - - - - - - rs10757045 9:19275390 A ENSESTG00000032846 ENSESTT00000083015 Transcript intron_variant - - - - - - rs10757045 9:19275390 A ENSESTG00000032696 ENSESTT00000082834 Transcript upstream_gene_variant - - - - - - DISTANCE=1060 rs10738537 9:19442689 G ENSESTG00000032802 ENSESTT00000082875 Transcript intron_variant - - - - - - rs10738537 9:19442689 G CCDS34992.1 CCDS34992.1 Transcript intron_variant - - - - - - rs10738537 9:19442689 G 340485 NM_001010887.2 Transcript intron_variant - - - - - - rs10117911 9:19636583 C ENSESTG00000032833 ENSESTT00000082963 Transcript intron_variant - - - - - - rs10117911 9:19636583 C CCDS6493.1 CCDS6493.1 Transcript intron_variant - - - - - - rs10117911 9:19636583 C 25769 NM_020344.3 Transcript intron_variant - - - - - - rs10117911 9:19636583 C CCDS55297.1 CCDS55297.1 Transcript intron_variant - - - - - - rs10117911 9:19636583 C 25769 NM_001193288.2 Transcript intron_variant - - - - - - rs2051133 9:19889261 C - - - intergenic_variant - - - - - - rs4977241 9:19997429 C - - - intergenic_variant - - - - - - rs2383132 9:20100287 G ENSESTG00000006740 ENSESTT00000017067 Transcript intron_variant - - - - - - rs383220 9:20348182 T CCDS6494.1 CCDS6494.1 Transcript intron_variant - - - - - - rs383220 9:20348182 T 4300 NM_004529.2 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016978 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000017015 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016987 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016970 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016944 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016999 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016984 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000017003 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016975 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000017011 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000017019 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000017004 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000017005 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016955 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016959 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016980 Transcript intron_variant - - - - - - rs6475481 9:20859068 T CCDS34993.1 CCDS34993.1 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016953 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016950 Transcript intron_variant - - - - - - rs6475481 9:20859068 T 54914 NM_017794.3 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000017009 Transcript intron_variant - - - - - - rs6475481 9:20859068 T ENSESTG00000006662 ENSESTT00000016941 Transcript intron_variant - - - - - - rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016978 Transcript downstream_gene_variant - - - - - - DISTANCE=1008 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000017015 Transcript missense_variant 868 818 273 T/S aCt/aGt - rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016987 Transcript downstream_gene_variant - - - - - - DISTANCE=3828 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016970 Transcript missense_variant 1929 1838 613 T/S aCt/aGt - rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016944 Transcript missense_variant 2247 2153 718 T/S aCt/aGt - rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016999 Transcript missense_variant 1943 1634 545 T/S aCt/aGt - rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016984 Transcript downstream_gene_variant - - - - - - DISTANCE=3828 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000017003 Transcript missense_variant 1943 1634 545 T/S aCt/aGt - rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016975 Transcript missense_variant 1929 1838 613 T/S aCt/aGt - rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000017011 Transcript downstream_gene_variant - - - - - - DISTANCE=3828 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000017019 Transcript downstream_gene_variant - - - - - - DISTANCE=3828 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000017004 Transcript downstream_gene_variant - - - - - - DISTANCE=1008 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000017005 Transcript downstream_gene_variant - - - - - - DISTANCE=1008 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016955 Transcript downstream_gene_variant - - - - - - DISTANCE=3828 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016959 Transcript downstream_gene_variant - - - - - - DISTANCE=3828 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016980 Transcript downstream_gene_variant - - - - - - DISTANCE=1008 rs7875872 9:20866974 G CCDS34993.1 CCDS34993.1 Transcript missense_variant 2153 2153 718 T/S aCt/aGt - PolyPhen=benign;SIFT=tolerated rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016953 Transcript downstream_gene_variant - - - - - - DISTANCE=1008 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016950 Transcript downstream_gene_variant - - - - - - DISTANCE=1008 rs7875872 9:20866974 G 54914 NM_017794.3 Transcript missense_variant 2516 2153 718 T/S aCt/aGt - PolyPhen=benign;SIFT=tolerated rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000017009 Transcript downstream_gene_variant - - - - - - DISTANCE=3828 rs7875872 9:20866974 G ENSESTG00000006662 ENSESTT00000016941 Transcript missense_variant 2247 2153 718 T/S aCt/aGt - rs4304410 9:20982503 G ENSESTG00000007861 ENSESTT00000019850 Transcript downstream_gene_variant - - - - - - DISTANCE=3428 rs4304410 9:20982503 G ENSESTG00000007699 ENSESTT00000019544 Transcript intron_variant - - - - - - rs4304410 9:20982503 G ENSESTG00000007699 ENSESTT00000019573 Transcript intron_variant - - - - - - rs4304410 9:20982503 G CCDS34993.1 CCDS34993.1 Transcript intron_variant - - - - - - rs4304410 9:20982503 G ENSESTG00000007699 ENSESTT00000019577 Transcript intron_variant - - - - - - rs4304410 9:20982503 G 54914 NM_017794.3 Transcript intron_variant - - - - - - rs4304410 9:20982503 G ENSESTG00000007699 ENSESTT00000019549 Transcript intron_variant - - - - - - rs4304410 9:20982503 G ENSESTG00000007699 ENSESTT00000019579 Transcript intron_variant - - - - - - rs4304410 9:20982503 G ENSESTG00000007699 ENSESTT00000019560 Transcript intron_variant - - - - - - rs10738579 9:21046289 A - - - intergenic_variant - - - - - - rs2990142 9:21350049 A CCDS6504.1 CCDS6504.1 Transcript downstream_gene_variant - - - - - - DISTANCE=268 rs2990142 9:21350049 A 3443 NM_021002.2 Transcript downstream_gene_variant - - - - - - DISTANCE=268 rs2383189 9:21440017 A ENSESTG00000007805 ENSESTT00000019728 Transcript intron_variant - - - - - - rs2383189 9:21440017 A ENSESTG00000007805 ENSESTT00000019721 Transcript intron_variant - - - - - - rs2383189 9:21440017 A CCDS6508.1 CCDS6508.1 Transcript upstream_gene_variant - - - - - - DISTANCE=490 rs2383189 9:21440017 A 3439 NM_024013.2 Transcript upstream_gene_variant - - - - - - DISTANCE=436 rs1953349 9:21689424 A - - - intergenic_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047534.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047535.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047538.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047537.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_003529.3 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047539.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047541.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A ENSESTG00000001342 ENSESTT00000003181 Transcript downstream_gene_variant - - - - - - DISTANCE=1522 rs649436 9:22031085 A 100048912 NR_047542.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047536.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047533.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047543.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047532.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs649436 9:22031085 A 100048912 NR_047540.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1679015 9:22207781 T ENSESTG00000001363 ENSESTT00000003219 Transcript intron_variant - - - - - - rs943400 9:22237501 G - - - intergenic_variant - - - - - - rs2383218 9:22332873 T - - - intergenic_variant - - - - - - rs547777 9:22472119 T - - - intergenic_variant - - - - - - rs552866 9:22680689 T ENSESTG00000001370 ENSESTT00000003228 Transcript intron_variant - - - - - - rs552866 9:22680689 T 441389 NR_038977.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1892209 9:22929314 A - - - intergenic_variant - - - - - - rs970080 9:22945838 T - - - intergenic_variant - - - - - - rs1856495 9:23045261 T - - - intergenic_variant - - - - - - rs1953825 9:23100590 T - - - intergenic_variant - - - - - - rs6475720 9:23250040 C - - - intergenic_variant - - - - - - rs6475731 9:23329685 T - - - intergenic_variant - - - - - - rs1576606 9:23330530 G - - - intergenic_variant - - - - - - rs7030769 9:23464185 T - - - intergenic_variant - - - - - - rs274919 9:23512481 C ENSESTG00000019450 ENSESTT00000048846 Transcript downstream_gene_variant - - - - - - DISTANCE=605 rs4246851 9:23597536 T - - - intergenic_variant - - - - - - rs10738676 9:23599872 A - - - intergenic_variant - - - - - - rs1226433 9:23929484 G - - - intergenic_variant - - - - - - rs4451399 9:23937393 C - - - intergenic_variant - - - - - - rs7025169 9:23989303 A - - - intergenic_variant - - - - - - rs604638 9:24232685 G - - - intergenic_variant - - - - - - rs524233 9:24236529 A - - - intergenic_variant - - - - - - rs6475810 9:24708144 T - - - intergenic_variant - - - - - - rs7852455 9:24733740 C - - - intergenic_variant - - - - - - rs10732344 9:24759508 G - - - intergenic_variant - - - - - - rs6475815 9:24766121 C - - - intergenic_variant - - - - - - rs4351496 9:24767807 T - - - intergenic_variant - - - - - - rs2383471 9:24863352 G - - - intergenic_variant - - - - - - rs3126946 9:25088777 A - - - intergenic_variant - - - - - - rs3126942 9:25180779 A - - - intergenic_variant - - - - - - rs1758716 9:25287414 G - - - intergenic_variant - - - - - - rs1662232 9:25381992 C - - - intergenic_variant - - - - - - rs517891 9:25928072 G - - - intergenic_variant - - - - - - rs9408111 9:26057449 A - - - intergenic_variant - - - - - - rs1160210 9:26477266 G - - - intergenic_variant - - - - - - rs1328424 9:26535079 C - - - intergenic_variant - - - - - - rs1810771 9:26567385 G - - - intergenic_variant - - - - - - rs4419902 9:26576561 G - - - intergenic_variant - - - - - - rs1028836 9:26582013 G - - - intergenic_variant - - - - - - rs1413823 9:26960775 A ENSESTG00000026269 ENSESTT00000066777 Transcript intron_variant - - - - - - rs1413823 9:26960775 A 80173 NM_025103.2 Transcript intron_variant - - - - - - rs1413823 9:26960775 A 80173 NM_001099222.1 Transcript intron_variant - - - - - - rs1413823 9:26960775 A 80173 NM_001099223.1 Transcript intron_variant - - - - - - rs1413823 9:26960775 A 80173 NM_001099224.1 Transcript intron_variant - - - - - - rs1413823 9:26960775 A ENSESTG00000026269 ENSESTT00000066765 Transcript intron_variant - - - - - - rs1413823 9:26960775 A CCDS43793.1 CCDS43793.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1191 rs1413823 9:26960775 A CCDS47955.1 CCDS47955.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1191 rs2814703 9:27436561 A - ENSR00001470000 RegulatoryFeature regulatory_region_variant - - - - - - rs2814703 9:27436561 A 79817 NM_024761.4 Transcript intron_variant - - - - - - rs2814703 9:27436561 A ENSESTG00000026700 ENSESTT00000067258 Transcript intron_variant - - - - - - rs2814703 9:27436561 A CCDS6520.1 CCDS6520.1 Transcript intron_variant - - - - - - rs2589050 9:27562352 C 203228 NM_018325.3 Transcript intron_variant - - - - - - rs2589050 9:27562352 C 203228 NM_145005.5 Transcript intron_variant - - - - - - rs2589050 9:27562352 C 203228 NM_001256054.1 Transcript intron_variant - - - - - - rs2589050 9:27562352 C ENSESTG00000026678 ENSESTT00000067200 Transcript intron_variant - - - - - - rs2589050 9:27562352 C CCDS6523.1 CCDS6523.1 Transcript intron_variant - - - - - - rs2589050 9:27562352 C CCDS6522.1 CCDS6522.1 Transcript intron_variant - - - - - - rs7034687 9:27892289 C - - - intergenic_variant - - - - - - rs7034966 9:28285124 T 158038 NM_001258282.1 Transcript intron_variant - - - - - - rs7034966 9:28285124 T 158038 NM_152570.2 Transcript intron_variant - - - - - - rs1331890 9:28456304 C 158038 NM_001258282.1 Transcript intron_variant - - - - - - rs1331890 9:28456304 C ENSESTG00000019479 ENSESTT00000048977 Transcript intron_variant - - - - - - rs1331890 9:28456304 C ENSESTG00000019479 ENSESTT00000048986 Transcript intron_variant - - - - - - rs1331890 9:28456304 C 158038 NM_152570.2 Transcript intron_variant - - - - - - rs823770 9:28621620 T 158038 NM_001258282.1 Transcript intron_variant - - - - - - rs823770 9:28621620 T ENSESTG00000019479 ENSESTT00000048977 Transcript intron_variant - - - - - - rs823770 9:28621620 T ENSESTG00000019479 ENSESTT00000048986 Transcript intron_variant - - - - - - rs823770 9:28621620 T 158038 NM_152570.2 Transcript intron_variant - - - - - - rs2768302 9:28791741 G 158038 NM_001258282.1 Transcript intron_variant - - - - - - rs320932 9:28890834 G 158038 NM_001258282.1 Transcript intron_variant - - - - - - rs320932 9:28890834 G 100126316 NR_030618.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1881 rs320932 9:28890834 G ENSESTG00000031466 ENSESTT00000079387 Transcript intron_variant - - - - - - rs900201 9:29649743 G - - - intergenic_variant - - - - - - rs1780062 9:30118844 T - - - intergenic_variant - - - - - - rs4879440 9:30480514 C - - - intergenic_variant - - - - - - rs375480 9:31752739 T - - - intergenic_variant - - - - - - rs1817766 9:31940058 C - - - intergenic_variant - - - - - - rs1490322 9:31952148 T - - - intergenic_variant - - - - - - rs409039 9:31984252 T - - - intergenic_variant - - - - - - rs1331235 9:32200357 C - - - intergenic_variant - - - - - - rs2783402 9:32531208 T ENSESTG00000005852 ENSESTT00000014847 Transcript intron_variant - - - - - - rs2783402 9:32531208 T 23586 NM_014314.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4886 rs10814371 9:36300810 G - - - intergenic_variant - - - - - - rs1547309 9:36603907 T 9833 NM_014791.3 Transcript intron_variant - - - - - - rs1547309 9:36603907 T 9833 NM_001256687.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T 9833 NM_001256692.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T 9833 NM_001256690.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T 9833 NM_001256688.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T ENSESTG00000000438 ENSESTT00000001136 Transcript intron_variant - - - - - - rs1547309 9:36603907 T CCDS59126.1 CCDS59126.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T CCDS59127.1 CCDS59127.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T CCDS59129.1 CCDS59129.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3680 rs1547309 9:36603907 T CCDS59124.1 CCDS59124.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T 9833 NM_001256691.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T CCDS59123.1 CCDS59123.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T CCDS6606.1 CCDS6606.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T 9833 NM_001256689.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T ENSESTG00000000438 ENSESTT00000001128 Transcript intron_variant - - - - - - rs1547309 9:36603907 T 9833 NM_001256685.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T CCDS59125.1 CCDS59125.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T CCDS59128.1 CCDS59128.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T 9833 NR_046337.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1547309 9:36603907 T 9833 NM_001256693.1 Transcript intron_variant - - - - - - rs1547309 9:36603907 T ENSESTG00000000438 ENSESTT00000001125 Transcript intron_variant - - - - - - rs10120818 9:36742823 C - - - intergenic_variant - - - - - - rs1176845 9:36813260 A - - - intergenic_variant - - - - - - rs4284114 9:36871260 T CCDS6607.1 CCDS6607.1 Transcript intron_variant - - - - - - rs4284114 9:36871260 T ENSESTG00000034239 ENSESTT00000086557 Transcript intron_variant - - - - - - rs4284114 9:36871260 T 5079 NM_016734.1 Transcript intron_variant - - - - - - rs913282 9:37483257 T ENSESTG00000034346 ENSESTT00000086912 Transcript upstream_gene_variant - - - - - - DISTANCE=2688 rs913282 9:37483257 T CCDS6611.1 CCDS6611.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2788 rs913282 9:37483257 T 64425 NM_022490.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2688 rs913282 9:37483257 T ENSESTG00000034346 ENSESTT00000086908 Transcript upstream_gene_variant - - - - - - DISTANCE=2688 rs7851820 9:37550759 G ENSESTG00000034434 ENSESTT00000087108 Transcript intron_variant - - - - - - rs7851820 9:37550759 G 26267 NM_012166.2 Transcript intron_variant - - - - - - rs776027 9:37915601 T ENSESTG00000020507 ENSESTT00000051530 Transcript downstream_gene_variant - - - - - - DISTANCE=3949 rs776027 9:37915601 T ENSESTG00000020507 ENSESTT00000051508 Transcript downstream_gene_variant - - - - - - DISTANCE=3949 rs776027 9:37915601 T 6461 NM_003028.2 Transcript downstream_gene_variant - - - - - - DISTANCE=294 rs776027 9:37915601 T ENSESTG00000020507 ENSESTT00000051528 Transcript downstream_gene_variant - - - - - - DISTANCE=3949 rs776027 9:37915601 T CCDS43806.1 CCDS43806.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4217 rs2810756 9:38160791 C - ENSR00001303456 RegulatoryFeature regulatory_region_variant - - - - - - rs2810756 9:38160791 C - - - intergenic_variant - - - - - - rs7041331 9:38292164 G - - - intergenic_variant - - - - - - rs6476708 9:38447291 G - - - intergenic_variant - - - - - - rs3005809 9:38634076 C - - - intergenic_variant - - - - - - rs7855071 9:65629772 G ENSESTG00000015430 ENSESTT00000038638 Transcript intron_variant - - - - - - rs603526 9:66709721 T ENSESTG00000001883 ENSESTT00000004682 Transcript downstream_gene_variant - - - - - - DISTANCE=1309 rs114906704 9:69072723 C - ENSR00001304670 RegulatoryFeature regulatory_region_variant - - - - - - rs114906704 9:69072723 C ENSESTG00000012632 ENSESTT00000031660 Transcript downstream_gene_variant - - - - - - DISTANCE=4797 rs114906704 9:69072723 C ENSESTG00000012632 ENSESTT00000031684 Transcript intron_variant - - - - - - rs114906704 9:69072723 C ENSESTG00000012632 ENSESTT00000031680 Transcript intron_variant - - - - - - rs373390 9:70996228 C ENSESTG00000026923 ENSESTT00000068075 Transcript intron_variant - - - - - - rs373390 9:70996228 C 5239 NM_021965.3 Transcript intron_variant - - - - - - rs373390 9:70996228 C ENSESTG00000026923 ENSESTT00000068029 Transcript intron_variant - - - - - - rs373390 9:70996228 C ENSESTG00000026923 ENSESTT00000068081 Transcript intron_variant - - - - - - rs373390 9:70996228 C ENSESTG00000026923 ENSESTT00000068040 Transcript intron_variant - - - - - - rs373390 9:70996228 C ENSESTG00000026923 ENSESTT00000068083 Transcript intron_variant - - - - - - rs373390 9:70996228 C ENSESTG00000026923 ENSESTT00000068018 Transcript intron_variant - - - - - - rs373390 9:70996228 C ENSESTG00000026923 ENSESTT00000068007 Transcript intron_variant - - - - - - rs373390 9:70996228 C ENSESTG00000026923 ENSESTT00000068090 Transcript intron_variant - - - - - - rs373390 9:70996228 C CCDS6622.2 CCDS6622.2 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068107 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068075 Transcript intron_variant - - - - - - rs62553004 9:71022713 A 5239 NM_021965.3 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068029 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068081 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068102 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068040 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068083 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068104 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068018 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068007 Transcript intron_variant - - - - - - rs62553004 9:71022713 A ENSESTG00000026923 ENSESTT00000068090 Transcript intron_variant - - - - - - rs62553004 9:71022713 A CCDS6622.2 CCDS6622.2 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068107 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068075 Transcript intron_variant - - - - - - rs265111 9:71035353 A 5239 NM_021965.3 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068029 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068081 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068102 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068040 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068083 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068104 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068018 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068007 Transcript intron_variant - - - - - - rs265111 9:71035353 A ENSESTG00000026923 ENSESTT00000068090 Transcript intron_variant - - - - - - rs265111 9:71035353 A CCDS6622.2 CCDS6622.2 Transcript intron_variant - - - - - - rs265075 9:71151948 C - ENSR00001470917 RegulatoryFeature regulatory_region_variant - - - - - - rs265075 9:71151948 C CCDS35040.1 CCDS35040.1 Transcript downstream_gene_variant - - - - - - DISTANCE=227 rs265075 9:71151948 C ENSESTG00000027091 ENSESTT00000068265 Transcript upstream_gene_variant - - - - - - DISTANCE=1303 rs265075 9:71151948 C 169693 NM_153237.1 Transcript 3_prime_UTR_variant 793 - - - - - rs265075 9:71151948 C ENSESTG00000027079 ENSESTT00000068245 Transcript intron_variant - - - - - - rs265075 9:71151948 C ENSESTG00000027079 ENSESTT00000068236 Transcript downstream_gene_variant - - - - - - DISTANCE=80 rs7029983 9:71214015 T - - - intergenic_variant - - - - - - rs4272453 9:71227878 G - - - intergenic_variant - - - - - - rs7038419 9:71326561 A ENSESTG00000026685 ENSESTT00000067221 Transcript downstream_gene_variant - - - - - - DISTANCE=3575 rs7038419 9:71326561 A ENSESTG00000026685 ENSESTT00000067197 Transcript intron_variant - - - - - - rs7038419 9:71326561 A 8395 NM_003558.2 Transcript intron_variant - - - - - - rs7038419 9:71326561 A ENSESTG00000026685 ENSESTT00000067210 Transcript intron_variant - - - - - - rs7038419 9:71326561 A ENSESTG00000026685 ENSESTT00000067177 Transcript downstream_gene_variant - - - - - - DISTANCE=3465 rs7030556 9:72335930 G CCDS47978.1 CCDS47978.1 Transcript intron_variant - - - - - - rs7030556 9:72335930 G 375743 NM_001099666.1 Transcript intron_variant - - - - - - rs7030556 9:72335930 G ENSESTG00000006470 ENSESTT00000016311 Transcript intron_variant - - - - - - rs7030556 9:72335930 G ENSESTG00000006470 ENSESTT00000016314 Transcript intron_variant - - - - - - rs10735564 9:72373624 G CCDS47978.1 CCDS47978.1 Transcript intron_variant - - - - - - rs10735564 9:72373624 G 375743 NM_001099666.1 Transcript intron_variant - - - - - - rs10735564 9:72373624 G ENSESTG00000006470 ENSESTT00000016311 Transcript intron_variant - - - - - - rs10735564 9:72373624 G ENSESTG00000006470 ENSESTT00000016316 Transcript intron_variant - - - - - - rs10735564 9:72373624 G ENSESTG00000006470 ENSESTT00000016314 Transcript intron_variant - - - - - - rs10735564 9:72373624 G ENSESTG00000006470 ENSESTT00000016292 Transcript splice_region_variant,intron_variant - - - - - - rs4744939 9:72397756 T - - - intergenic_variant - - - - - - rs4744579 9:72556735 C - - - intergenic_variant - - - - - - rs10746840 9:72936071 G 23137 NM_015110.3 Transcript intron_variant - - - - - - rs10746840 9:72936071 G ENSESTG00000005528 ENSESTT00000014122 Transcript intron_variant - - - - - - rs10746840 9:72936071 G ENSESTG00000005528 ENSESTT00000014119 Transcript intron_variant - - - - - - rs10746840 9:72936071 G ENSESTG00000005592 ENSESTT00000014217 Transcript downstream_gene_variant - - - - - - DISTANCE=1325 rs10746840 9:72936071 G CCDS6632.1 CCDS6632.1 Transcript intron_variant - - - - - - rs12340612 9:73221428 T CCDS6636.1 CCDS6636.1 Transcript intron_variant - - - - - - rs12340612 9:73221428 T 80036 NM_020952.4 Transcript intron_variant - - - - - - rs12340612 9:73221428 T 80036 NM_001007471.2 Transcript intron_variant - - - - - - rs12340612 9:73221428 T 80036 NM_206946.3 Transcript intron_variant - - - - - - rs12340612 9:73221428 T 80036 NM_206944.3 Transcript intron_variant - - - - - - rs12340612 9:73221428 T 80036 NM_024971.5 Transcript intron_variant - - - - - - rs12340612 9:73221428 T 80036 NM_206947.3 Transcript intron_variant - - - - - - rs12340612 9:73221428 T CCDS6635.1 CCDS6635.1 Transcript intron_variant - - - - - - rs12340612 9:73221428 T 80036 NM_206945.3 Transcript intron_variant - - - - - - rs12340612 9:73221428 T CCDS6634.1 CCDS6634.1 Transcript intron_variant - - - - - - rs12340612 9:73221428 T CCDS43835.1 CCDS43835.1 Transcript intron_variant - - - - - - rs10868878 9:73308794 T CCDS6636.1 CCDS6636.1 Transcript intron_variant - - - - - - rs10868878 9:73308794 T 80036 NM_020952.4 Transcript intron_variant - - - - - - rs10868878 9:73308794 T 80036 NM_001007471.2 Transcript intron_variant - - - - - - rs10868878 9:73308794 T 80036 NM_206946.3 Transcript intron_variant - - - - - - rs10868878 9:73308794 T 80036 NM_206944.3 Transcript intron_variant - - - - - - rs10868878 9:73308794 T 80036 NM_024971.5 Transcript intron_variant - - - - - - rs10868878 9:73308794 T 80036 NM_206947.3 Transcript intron_variant - - - - - - rs10868878 9:73308794 T CCDS6635.1 CCDS6635.1 Transcript intron_variant - - - - - - rs10868878 9:73308794 T 80036 NM_206945.3 Transcript intron_variant - - - - - - rs10868878 9:73308794 T CCDS6634.1 CCDS6634.1 Transcript intron_variant - - - - - - rs10868878 9:73308794 T CCDS43835.1 CCDS43835.1 Transcript intron_variant - - - - - - rs505221 9:73436425 G CCDS6637.1 CCDS6637.1 Transcript intron_variant - - - - - - rs505221 9:73436425 G CCDS6636.1 CCDS6636.1 Transcript intron_variant - - - - - - rs505221 9:73436425 G 80036 NM_001007470.1 Transcript intron_variant - - - - - - rs505221 9:73436425 G 80036 NM_206946.3 Transcript intron_variant - - - - - - rs505221 9:73436425 G 80036 NM_206944.3 Transcript intron_variant - - - - - - rs505221 9:73436425 G 80036 NM_206947.3 Transcript intron_variant - - - - - - rs505221 9:73436425 G CCDS6635.1 CCDS6635.1 Transcript intron_variant - - - - - - rs505221 9:73436425 G CCDS6634.1 CCDS6634.1 Transcript intron_variant - - - - - - rs505221 9:73436425 G CCDS43835.1 CCDS43835.1 Transcript intron_variant - - - - - - rs505221 9:73436425 G 80036 NM_020952.4 Transcript intron_variant - - - - - - rs505221 9:73436425 G 80036 NM_001007471.2 Transcript intron_variant - - - - - - rs505221 9:73436425 G ENSESTG00000005573 ENSESTT00000014187 Transcript intron_variant - - - - - - rs505221 9:73436425 G 80036 NM_206948.2 Transcript intron_variant - - - - - - rs505221 9:73436425 G 80036 NM_024971.5 Transcript intron_variant - - - - - - rs505221 9:73436425 G 80036 NM_206945.3 Transcript intron_variant - - - - - - rs505221 9:73436425 G ENSESTG00000005573 ENSESTT00000014183 Transcript intron_variant - - - - - - rs1329775 9:73759085 A - - - intergenic_variant - - - - - - rs1927944 9:73867687 C - - - intergenic_variant - - - - - - rs1110840 9:74384641 C - ENSR00001471154 RegulatoryFeature regulatory_region_variant - - - - - - rs1110840 9:74384641 C - MA0147.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=2;MOTIF_NAME=Jaspar_Matrix_Cmyc:MA0147.1;HIGH_INF_POS=N;MOTIF_SCORE_CHANGE=-0.017 rs1110840 9:74384641 C ENSESTG00000013494 ENSESTT00000033798 Transcript upstream_gene_variant - - - - - - DISTANCE=1214 rs1110840 9:74384641 C 23670 NM_001135820.1 Transcript upstream_gene_variant - - - - - - DISTANCE=841 rs1110840 9:74384641 C ENSESTG00000013494 ENSESTT00000033781 Transcript intron_variant - - - - - - rs1110840 9:74384641 C 23670 NM_013390.2 Transcript upstream_gene_variant - - - - - - DISTANCE=841 rs1110840 9:74384641 C ENSESTG00000013494 ENSESTT00000033790 Transcript upstream_gene_variant - - - - - - DISTANCE=1212 rs6560231 9:74386444 T ENSESTG00000013494 ENSESTT00000033798 Transcript upstream_gene_variant - - - - - - DISTANCE=3017 rs6560231 9:74386444 T 23670 NM_001135820.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2644 rs6560231 9:74386444 T ENSESTG00000013494 ENSESTT00000033781 Transcript intron_variant - - - - - - rs6560231 9:74386444 T 23670 NM_013390.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2644 rs6560231 9:74386444 T ENSESTG00000013494 ENSESTT00000033790 Transcript upstream_gene_variant - - - - - - DISTANCE=3015 rs1524379 9:74487316 A ENSESTG00000013477 ENSESTT00000033758 Transcript intron_variant - - - - - - rs1524379 9:74487316 A 51104 NM_016014.2 Transcript intron_variant - - - - - - rs1524379 9:74487316 A ENSESTG00000013477 ENSESTT00000033753 Transcript intron_variant - - - - - - rs1524379 9:74487316 A CCDS35043.1 CCDS35043.1 Transcript intron_variant - - - - - - rs1524379 9:74487316 A CCDS35042.1 CCDS35042.1 Transcript intron_variant - - - - - - rs1524379 9:74487316 A 51104 NM_001025780.1 Transcript intron_variant - - - - - - rs6560258 9:74830230 G 9615 NM_001242506.2 Transcript intron_variant - - - - - - rs6560258 9:74830230 G ENSESTG00000006810 ENSESTT00000017352 Transcript downstream_gene_variant - - - - - - DISTANCE=1371 rs6560258 9:74830230 G 9615 NM_004293.4 Transcript intron_variant - - - - - - rs6560258 9:74830230 G 9615 NM_001242507.2 Transcript intron_variant - - - - - - rs6560258 9:74830230 G CCDS6641.1 CCDS6641.1 Transcript intron_variant - - - - - - rs6560258 9:74830230 G 9615 NM_001242505.2 Transcript intron_variant - - - - - - rs6560258 9:74830230 G CCDS56577.1 CCDS56577.1 Transcript intron_variant - - - - - - rs6560258 9:74830230 G CCDS56576.1 CCDS56576.1 Transcript intron_variant - - - - - - rs2310330 9:75714026 T ENSESTG00000006449 ENSESTT00000016249 Transcript intron_variant - - - - - - rs10781112 9:75717030 C ENSESTG00000006449 ENSESTT00000016249 Transcript intron_variant - - - - - - rs4744687 9:75999583 G - - - intergenic_variant - - - - - - rs1414162 9:76018329 A - - - intergenic_variant - - - - - - rs664754 9:76854673 A - - - intergenic_variant - - - - - - rs2376152 9:77051907 T - - - intergenic_variant - - - - - - rs4351473 9:77110552 T CCDS6646.1 CCDS6646.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2341 rs4351473 9:77110552 T 6096 NM_006914.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1700 rs1176812 9:77555782 C - ENSR00001305901 RegulatoryFeature regulatory_region_variant - - - - - - rs1176812 9:77555782 C - - - intergenic_variant - - - - - - rs2800243 9:77622963 A 138199 NM_152420.1 Transcript intron_variant - - - - - - rs2800243 9:77622963 A CCDS6649.1 CCDS6649.1 Transcript intron_variant - - - - - - rs4745392 9:77868493 G - - - intergenic_variant - - - - - - rs2185229 9:78684005 C CCDS55320.1 CCDS55320.1 Transcript intron_variant - - - - - - rs2185229 9:78684005 C ENSESTG00000019201 ENSESTT00000048453 Transcript intron_variant - - - - - - rs2185229 9:78684005 C 5125 NM_001190482.1 Transcript intron_variant - - - - - - rs2185229 9:78684005 C CCDS6652.1 CCDS6652.1 Transcript intron_variant - - - - - - rs2185229 9:78684005 C 5125 NM_006200.3 Transcript intron_variant - - - - - - rs2185229 9:78684005 C ENSESTG00000019679 ENSESTT00000049374 Transcript intron_variant - - - - - - rs2185229 9:78684005 C ENSESTG00000019201 ENSESTT00000048513 Transcript intron_variant - - - - - - rs2185229 9:78684005 C ENSESTG00000019679 ENSESTT00000049392 Transcript intron_variant - - - - - - rs2803406 9:78870983 C - ENSR00001471416 RegulatoryFeature regulatory_region_variant - - - - - - rs2803406 9:78870983 C ENSESTG00000019339 ENSESTT00000048663 Transcript intron_variant - - - - - - rs2803406 9:78870983 C CCDS55320.1 CCDS55320.1 Transcript intron_variant - - - - - - rs2803406 9:78870983 C 5125 NM_001190482.1 Transcript intron_variant - - - - - - rs2490582 9:79009106 C - ENSR00001306041 RegulatoryFeature regulatory_region_variant - - - - - - rs2490582 9:79009106 C 653162 NR_026890.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4409 rs2490582 9:79009106 C CCDS35044.2 CCDS35044.2 Transcript upstream_gene_variant - - - - - - DISTANCE=19 rs2490582 9:79009106 C 55312 NM_018339.5 Transcript 5_prime_UTR_variant 339 - - - - - rs2771027 9:79161031 C - - - intergenic_variant - - - - - - rs10747002 9:79438012 C ENSESTG00000019448 ENSESTT00000048897 Transcript intron_variant - - - - - - rs10747002 9:79438012 C CCDS47982.1 CCDS47982.1 Transcript intron_variant - - - - - - rs10747002 9:79438012 C 158471 NM_015225.2 Transcript intron_variant - - - - - - rs3936973 9:80254270 T ENSESTG00000033885 ENSESTT00000085663 Transcript intron_variant - - - - - - rs3936973 9:80254270 T CCDS6657.1 CCDS6657.1 Transcript intron_variant - - - - - - rs3936973 9:80254270 T 9630 NM_004297.3 Transcript intron_variant - - - - - - rs4422835 9:80255953 T ENSESTG00000033885 ENSESTT00000085663 Transcript intron_variant - - - - - - rs4422835 9:80255953 T CCDS6657.1 CCDS6657.1 Transcript intron_variant - - - - - - rs4422835 9:80255953 T 9630 NM_004297.3 Transcript intron_variant - - - - - - rs273441 9:81929934 T - - - intergenic_variant - - - - - - rs2791566 9:82189914 C - ENSR00001471689 RegulatoryFeature regulatory_region_variant - - - - - - rs2791566 9:82189914 C ENSESTG00000008023 ENSESTT00000020286 Transcript downstream_gene_variant - - - - - - DISTANCE=2163 rs2791566 9:82189914 C ENSESTG00000008023 ENSESTT00000020332 Transcript upstream_gene_variant - - - - - - DISTANCE=780 rs2791566 9:82189914 C ENSESTG00000008023 ENSESTT00000020326 Transcript intron_variant - - - - - - rs2791566 9:82189914 C ENSESTG00000008023 ENSESTT00000020300 Transcript intron_variant - - - - - - rs2791566 9:82189914 C 7091 NM_007005.3 Transcript intron_variant - - - - - - rs2791566 9:82189914 C ENSESTG00000008023 ENSESTT00000020320 Transcript intron_variant - - - - - - rs2791566 9:82189914 C ENSESTG00000008023 ENSESTT00000020298 Transcript intron_variant - - - - - - rs2791566 9:82189914 C ENSESTG00000008023 ENSESTT00000020337 Transcript upstream_gene_variant - - - - - - DISTANCE=781 rs2791566 9:82189914 C CCDS43837.1 CCDS43837.1 Transcript intron_variant - - - - - - rs1419272 9:83103859 G - - - intergenic_variant - - - - - - rs4404988 9:83373689 A - - - intergenic_variant - - - - - - rs4097678 9:83373995 C - - - intergenic_variant - - - - - - rs912458 9:83416986 A - - - intergenic_variant - - - - - - rs1175340 9:83663404 A - - - intergenic_variant - - - - - - rs1571486 9:83999987 C - - - intergenic_variant - - - - - - rs1041201 9:84733547 G - - - intergenic_variant - - - - - - rs6559651 9:84751189 A - - - intergenic_variant - - - - - - rs574782 9:85347883 C - - - intergenic_variant - - - - - - rs1354251 9:85604659 T ENSESTG00000020435 ENSESTT00000051281 Transcript intron_variant - - - - - - rs1354251 9:85604659 T CCDS6662.1 CCDS6662.1 Transcript intron_variant - - - - - - rs1354251 9:85604659 T 158158 NM_152573.2 Transcript intron_variant - - - - - - rs6559766 9:86713227 T ENSESTG00000002816 ENSESTT00000006977 Transcript intron_variant - - - - - - rs2225583 9:87155208 C - - - intergenic_variant - - - - - - rs1201365 9:87313004 G 4915 NM_006180.3 Transcript intron_variant - - - - - - rs1201365 9:87313004 G 4915 NM_001018065.2 Transcript intron_variant - - - - - - rs1201365 9:87313004 G CCDS35051.1 CCDS35051.1 Transcript intron_variant - - - - - - rs1201365 9:87313004 G ENSESTG00000002769 ENSESTT00000006899 Transcript intron_variant - - - - - - rs1201365 9:87313004 G 4915 NM_001018064.1 Transcript intron_variant - - - - - - rs1201365 9:87313004 G CCDS35053.1 CCDS35053.1 Transcript intron_variant - - - - - - rs1201365 9:87313004 G 4915 NM_001007097.1 Transcript intron_variant - - - - - - rs1201365 9:87313004 G CCDS35052.1 CCDS35052.1 Transcript intron_variant - - - - - - rs1201365 9:87313004 G 4915 NM_001018066.2 Transcript intron_variant - - - - - - rs1201365 9:87313004 G CCDS6671.1 CCDS6671.1 Transcript intron_variant - - - - - - rs1201365 9:87313004 G CCDS35050.1 CCDS35050.1 Transcript intron_variant - - - - - - rs7031536 9:87528998 G 4915 NM_006180.3 Transcript intron_variant - - - - - - rs7031536 9:87528998 G ENSESTG00000002769 ENSESTT00000006912 Transcript intron_variant - - - - - - rs7031536 9:87528998 G CCDS6671.1 CCDS6671.1 Transcript intron_variant - - - - - - rs7031536 9:87528998 G 4915 NM_001018064.1 Transcript intron_variant - - - - - - rs7031536 9:87528998 G CCDS35050.1 CCDS35050.1 Transcript intron_variant - - - - - - rs598891 9:88211771 C 23287 NM_015239.2 Transcript intron_variant - - - - - - rs598891 9:88211771 C ENSESTG00000006768 ENSESTT00000017250 Transcript intron_variant - - - - - - rs598891 9:88211771 C CCDS6672.1 CCDS6672.1 Transcript intron_variant - - - - - - rs4877991 9:89176722 C - - - intergenic_variant - - - - - - rs4877992 9:89176840 C - - - intergenic_variant - - - - - - rs4523355 9:90974199 G - - - intergenic_variant - - - - - - rs1288651 9:91415219 A - ENSR00001307783 RegulatoryFeature regulatory_region_variant - - - - - - rs1288651 9:91415219 A - - - intergenic_variant - - - - - - rs7043711 9:91604469 G - ENSR00001307818 RegulatoryFeature regulatory_region_variant - - - - - - rs7043711 9:91604469 G CCDS47989.1 CCDS47989.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1442 rs7043711 9:91604469 G ENSESTG00000029240 ENSESTT00000073677 Transcript upstream_gene_variant - - - - - - DISTANCE=1374 rs7043711 9:91604469 G 1903 NM_005226.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1855 rs7043711 9:91604469 G ENSESTG00000029240 ENSESTT00000073661 Transcript upstream_gene_variant - - - - - - DISTANCE=1295 rs7043711 9:91604469 G CCDS35062.1 CCDS35062.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1442 rs7043711 9:91604469 G 286223 NM_001001938.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1309 rs7043711 9:91604469 G 286223 NM_001142413.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1309 rs1530374 9:92695260 T - - - intergenic_variant - - - - - - rs7045428 9:93269165 G ENSESTG00000033103 ENSESTT00000083639 Transcript upstream_gene_variant - - - - - - DISTANCE=1124 rs7045428 9:93269165 G ENSESTG00000033098 ENSESTT00000083630 Transcript downstream_gene_variant - - - - - - DISTANCE=384 rs7045428 9:93269165 G 340515 NR_034157.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs290231 9:93603204 C 6850 NM_001174167.1 Transcript intron_variant - - - - - - rs290231 9:93603204 C ENSESTG00000030726 ENSESTT00000077527 Transcript intron_variant - - - - - - rs290231 9:93603204 C ENSESTG00000030726 ENSESTT00000077474 Transcript intron_variant - - - - - - rs290231 9:93603204 C ENSESTG00000030726 ENSESTT00000077485 Transcript intron_variant - - - - - - rs290231 9:93603204 C CCDS47992.1 CCDS47992.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2977 rs290231 9:93603204 C 6850 NM_001135052.2 Transcript intron_variant - - - - - - rs290231 9:93603204 C 6850 NM_003177.5 Transcript intron_variant - - - - - - rs290231 9:93603204 C 6850 NM_001174168.1 Transcript intron_variant - - - - - - rs290231 9:93603204 C ENSESTG00000030726 ENSESTT00000077521 Transcript intron_variant - - - - - - rs290231 9:93603204 C ENSESTG00000030726 ENSESTT00000077509 Transcript intron_variant - - - - - - rs290231 9:93603204 C CCDS6688.1 CCDS6688.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2977 rs290231 9:93603204 C ENSESTG00000030726 ENSESTT00000077495 Transcript intron_variant - - - - - - rs1760132 9:93639803 G 6850 NM_001174167.1 Transcript intron_variant - - - - - - rs1760132 9:93639803 G ENSESTG00000030726 ENSESTT00000077558 Transcript intron_variant - - - - - - rs1760132 9:93639803 G ENSESTG00000030726 ENSESTT00000077527 Transcript intron_variant - - - - - - rs1760132 9:93639803 G ENSESTG00000030726 ENSESTT00000077474 Transcript intron_variant - - - - - - rs1760132 9:93639803 G ENSESTG00000030726 ENSESTT00000077485 Transcript intron_variant - - - - - - rs1760132 9:93639803 G ENSESTG00000030726 ENSESTT00000077545 Transcript intron_variant - - - - - - rs1760132 9:93639803 G CCDS47992.1 CCDS47992.1 Transcript intron_variant - - - - - - rs1760132 9:93639803 G 6850 NM_001135052.2 Transcript intron_variant - - - - - - rs1760132 9:93639803 G 6850 NM_003177.5 Transcript intron_variant - - - - - - rs1760132 9:93639803 G 6850 NM_001174168.1 Transcript intron_variant - - - - - - rs1760132 9:93639803 G ENSESTG00000030726 ENSESTT00000077521 Transcript intron_variant - - - - - - rs1760132 9:93639803 G ENSESTG00000030726 ENSESTT00000077509 Transcript intron_variant - - - - - - rs1760132 9:93639803 G CCDS6688.1 CCDS6688.1 Transcript intron_variant - - - - - - rs1760132 9:93639803 G ENSESTG00000030726 ENSESTT00000077571 Transcript downstream_gene_variant - - - - - - DISTANCE=2677 rs1760132 9:93639803 G ENSESTG00000030726 ENSESTT00000077495 Transcript intron_variant - - - - - - rs1675299 9:93678885 A - ENSR00001472566 RegulatoryFeature regulatory_region_variant - - - - - - rs1675299 9:93678885 A - - - intergenic_variant - - - - - - rs7018803 9:93902307 G ENSESTG00000031033 ENSESTT00000078098 Transcript intron_variant - - - - - - rs7018803 9:93902307 G ENSESTG00000031033 ENSESTT00000078091 Transcript intron_variant - - - - - - rs814028 9:94145945 A - - - intergenic_variant - - - - - - rs331371 9:95275574 A 1842 NM_001197295.1 Transcript intron_variant - - - - - - rs331371 9:95275574 A ENSESTG00000024230 ENSESTT00000061273 Transcript downstream_gene_variant - - - - - - DISTANCE=4136 rs331371 9:95275574 A 1842 NM_001393.3 Transcript intron_variant - - - - - - rs331371 9:95275574 A 401541 NM_001012267.1 Transcript intron_variant - - - - - - rs331371 9:95275574 A ENSESTG00000024230 ENSESTT00000061260 Transcript downstream_gene_variant - - - - - - DISTANCE=1877 rs331371 9:95275574 A CCDS35063.1 CCDS35063.1 Transcript intron_variant - - - - - - rs331371 9:95275574 A CCDS6698.1 CCDS6698.1 Transcript intron_variant - - - - - - rs331371 9:95275574 A CCDS56578.1 CCDS56578.1 Transcript intron_variant - - - - - - rs331371 9:95275574 A 1842 NM_001197296.1 Transcript intron_variant - - - - - - rs331372 9:95285731 G 1842 NM_001197295.1 Transcript intron_variant - - - - - - rs331372 9:95285731 G ENSESTG00000024230 ENSESTT00000061273 Transcript intron_variant - - - - - - rs331372 9:95285731 G 1842 NM_001393.3 Transcript intron_variant - - - - - - rs331372 9:95285731 G 401541 NM_001012267.1 Transcript intron_variant - - - - - - rs331372 9:95285731 G ENSESTG00000024230 ENSESTT00000061260 Transcript intron_variant - - - - - - rs331372 9:95285731 G CCDS35063.1 CCDS35063.1 Transcript intron_variant - - - - - - rs331372 9:95285731 G CCDS6698.1 CCDS6698.1 Transcript upstream_gene_variant - - - - - - DISTANCE=583 rs331372 9:95285731 G 100616351 NR_039817.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4535 rs331372 9:95285731 G CCDS56578.1 CCDS56578.1 Transcript upstream_gene_variant - - - - - - DISTANCE=583 rs331372 9:95285731 G 1842 NM_001197296.1 Transcript intron_variant - - - - - - rs331373 9:95295278 C 1842 NM_001197295.1 Transcript intron_variant - - - - - - rs331373 9:95295278 C ENSESTG00000024230 ENSESTT00000061273 Transcript intron_variant - - - - - - rs331373 9:95295278 C 1842 NM_001393.3 Transcript intron_variant - - - - - - rs331373 9:95295278 C 401541 NM_001012267.1 Transcript intron_variant - - - - - - rs331373 9:95295278 C ENSESTG00000024230 ENSESTT00000061260 Transcript intron_variant - - - - - - rs331373 9:95295278 C CCDS35063.1 CCDS35063.1 Transcript intron_variant - - - - - - rs331373 9:95295278 C 100616351 NR_039817.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4938 rs331373 9:95295278 C 1842 NM_001197296.1 Transcript intron_variant - - - - - - rs2617223 9:96160270 A - ENSR00001472756 RegulatoryFeature regulatory_region_variant - - - - - - rs2617223 9:96160270 A - - - intergenic_variant - - - - - - rs2790424 9:97250653 C - - - intergenic_variant - - - - - - rs2987898 9:97368301 C ENSESTG00000018399 ENSESTT00000046401 Transcript intron_variant - - - - - - rs2987898 9:97368301 C ENSESTG00000018399 ENSESTT00000046379 Transcript intron_variant - - - - - - rs2987898 9:97368301 C CCDS6712.1 CCDS6712.1 Transcript intron_variant - - - - - - rs2987898 9:97368301 C 2203 NM_001127628.1 Transcript intron_variant - - - - - - rs2987898 9:97368301 C 2203 NM_000507.3 Transcript intron_variant - - - - - - rs2987898 9:97368301 C ENSESTG00000018399 ENSESTT00000046369 Transcript intron_variant - - - - - - rs454554 9:97540668 T CCDS6713.1 CCDS6713.1 Transcript intron_variant - - - - - - rs454554 9:97540668 T CCDS55327.1 CCDS55327.1 Transcript intron_variant - - - - - - rs454554 9:97540668 T 84909 NM_001193331.2 Transcript intron_variant - - - - - - rs454554 9:97540668 T CCDS55328.1 CCDS55328.1 Transcript intron_variant - - - - - - rs454554 9:97540668 T 84909 NM_001193329.1 Transcript intron_variant - - - - - - rs454554 9:97540668 T 84909 NM_032823.5 Transcript intron_variant - - - - - - rs454554 9:97540668 T ENSESTG00000025741 ENSESTT00000064933 Transcript intron_variant - - - - - - rs701000 9:98422747 C - - - intergenic_variant - - - - - - rs2770839 9:98650725 T CCDS35072.1 CCDS35072.1 Transcript intron_variant - - - - - - rs2770839 9:98650725 T ENSESTG00000000461 ENSESTT00000001150 Transcript intron_variant - - - - - - rs2770839 9:98650725 T ENSESTG00000000461 ENSESTT00000001152 Transcript intron_variant - - - - - - rs2770839 9:98650725 T 375748 NM_001010895.2 Transcript intron_variant - - - - - - rs7033190 9:99893530 A ENSESTG00000020558 ENSESTT00000051538 Transcript intron_variant - - - - - - rs2615142 9:100050502 T 57653 NR_036528.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2615142 9:100050502 T ENSESTG00000019793 ENSESTT00000049619 Transcript upstream_gene_variant - - - - - - DISTANCE=2373 rs2615142 9:100050502 T 57653 NR_036527.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2615142 9:100050502 T 57653 NR_036529.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2615142 9:100050502 T 100499484 NR_036526.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1888149 9:100262338 C ENSESTG00000020143 ENSESTT00000050655 Transcript upstream_gene_variant - - - - - - DISTANCE=1610 rs1888149 9:100262338 C ENSESTG00000020143 ENSESTT00000050637 Transcript upstream_gene_variant - - - - - - DISTANCE=1124 rs1888149 9:100262338 C 7111 NM_001166116.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1124 rs1888149 9:100262338 C ENSESTG00000020115 ENSESTT00000050456 Transcript downstream_gene_variant - - - - - - DISTANCE=3937 rs1888149 9:100262338 C 7111 NM_003275.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1583 rs1888149 9:100262338 C CCDS6725.1 CCDS6725.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4173 rs1888149 9:100262338 C ENSESTG00000020115 ENSESTT00000050467 Transcript downstream_gene_variant - - - - - - DISTANCE=4089 rs1888149 9:100262338 C ENSESTG00000020143 ENSESTT00000050628 Transcript upstream_gene_variant - - - - - - DISTANCE=1124 rs1888149 9:100262338 C 23424 NM_014290.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3931 rs1888149 9:100262338 C ENSESTG00000020143 ENSESTT00000050662 Transcript upstream_gene_variant - - - - - - DISTANCE=1610 rs2779596 9:101225970 T CCDS6736.1 CCDS6736.1 Transcript intron_variant - - - - - - rs2779596 9:101225970 T 9568 NM_005458.7 Transcript intron_variant - - - - - - rs2779596 9:101225970 T ENSESTG00000000321 ENSESTT00000000826 Transcript intron_variant - - - - - - rs2779596 9:101225970 T ENSESTG00000000321 ENSESTT00000000833 Transcript intron_variant - - - - - - rs2779596 9:101225970 T ENSESTG00000000321 ENSESTT00000000813 Transcript intron_variant - - - - - - rs2779596 9:101225970 T ENSESTG00000000321 ENSESTT00000000831 Transcript intron_variant - - - - - - rs2779596 9:101225970 T ENSESTG00000000321 ENSESTT00000000812 Transcript intron_variant - - - - - - rs2779596 9:101225970 T ENSESTG00000000321 ENSESTT00000000824 Transcript intron_variant - - - - - - rs2779566 9:101279549 G CCDS6736.1 CCDS6736.1 Transcript intron_variant - - - - - - rs2779566 9:101279549 G 9568 NM_005458.7 Transcript intron_variant - - - - - - rs2779566 9:101279549 G ENSESTG00000000321 ENSESTT00000000826 Transcript intron_variant - - - - - - rs2779566 9:101279549 G ENSESTG00000000321 ENSESTT00000000833 Transcript intron_variant - - - - - - rs2779566 9:101279549 G ENSESTG00000000321 ENSESTT00000000813 Transcript intron_variant - - - - - - rs2779566 9:101279549 G ENSESTG00000000321 ENSESTT00000000819 Transcript intron_variant - - - - - - rs2779566 9:101279549 G ENSESTG00000000321 ENSESTT00000000831 Transcript intron_variant - - - - - - rs2779566 9:101279549 G ENSESTG00000000321 ENSESTT00000000812 Transcript intron_variant - - - - - - rs2779566 9:101279549 G ENSESTG00000000321 ENSESTT00000000824 Transcript intron_variant - - - - - - rs337562 9:101515112 G CCDS43856.1 CCDS43856.1 Transcript intron_variant - - - - - - rs337562 9:101515112 G 203286 NM_173551.3 Transcript intron_variant - - - - - - rs337562 9:101515112 G ENSESTG00000002256 ENSESTT00000005672 Transcript intron_variant - - - - - - rs337562 9:101515112 G ENSESTG00000002256 ENSESTT00000005662 Transcript intron_variant - - - - - - rs7019194 9:102329227 C ENSESTG00000002220 ENSESTT00000005572 Transcript intron_variant - - - - - - rs4743362 9:102379377 T ENSESTG00000002220 ENSESTT00000005566 Transcript intron_variant - - - - - - rs4743362 9:102379377 T ENSESTG00000002220 ENSESTT00000005572 Transcript intron_variant - - - - - - rs694479 9:103766834 C - - - intergenic_variant - - - - - - rs7037661 9:104132911 C ENSESTG00000027851 ENSESTT00000070111 Transcript intron_variant - - - - - - rs7037661 9:104132911 C 570 NM_001127610.1 Transcript intron_variant - - - - - - rs7037661 9:104132911 C 570 NM_001701.3 Transcript intron_variant - - - - - - rs7037661 9:104132911 C CCDS6752.1 CCDS6752.1 Transcript intron_variant - - - - - - rs320270 9:104856666 A - - - intergenic_variant - - - - - - rs320170 9:104880496 G - - - intergenic_variant - - - - - - rs1593334 9:105163562 A - - - intergenic_variant - - - - - - rs7864937 9:105442729 G - - - intergenic_variant - - - - - - rs2066262 9:105772746 T CCDS35085.1 CCDS35085.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4786 rs2066262 9:105772746 T 1539 NM_001340.3 Transcript intron_variant - - - - - - rs7022982 9:106397573 T - - - intergenic_variant - - - - - - rs417560 9:106509341 A - - - intergenic_variant - - - - - - rs1470047 9:106583167 T - - - intergenic_variant - - - - - - rs7043183 9:108135718 A 23446 NM_080546.3 Transcript intron_variant - - - - - - rs7043183 9:108135718 A ENSESTG00000011571 ENSESTT00000029081 Transcript intron_variant - - - - - - rs7043183 9:108135718 A ENSESTG00000011571 ENSESTT00000029060 Transcript intron_variant - - - - - - rs7043183 9:108135718 A ENSESTG00000011571 ENSESTT00000029073 Transcript intron_variant - - - - - - rs7043183 9:108135718 A ENSESTG00000011571 ENSESTT00000029085 Transcript intron_variant - - - - - - rs7043183 9:108135718 A ENSESTG00000011571 ENSESTT00000029071 Transcript intron_variant - - - - - - rs7043183 9:108135718 A ENSESTG00000011571 ENSESTT00000029088 Transcript intron_variant - - - - - - rs7043183 9:108135718 A ENSESTG00000011571 ENSESTT00000029074 Transcript intron_variant - - - - - - rs7043183 9:108135718 A CCDS6763.1 CCDS6763.1 Transcript intron_variant - - - - - - rs7043183 9:108135718 A ENSESTG00000011571 ENSESTT00000029080 Transcript intron_variant - - - - - - rs2031909 9:108192165 G ENSESTG00000011571 ENSESTT00000029085 Transcript intron_variant - - - - - - rs2031909 9:108192165 G ENSESTG00000011571 ENSESTT00000029060 Transcript intron_variant - - - - - - rs2031909 9:108192165 G ENSESTG00000011571 ENSESTT00000029080 Transcript intron_variant - - - - - - rs2031909 9:108192165 G ENSESTG00000011571 ENSESTT00000029073 Transcript intron_variant - - - - - - rs1484379 9:109166550 C - - - intergenic_variant - - - - - - rs4237182 9:109186415 C - - - intergenic_variant - - - - - - rs1510282 9:109703816 A ENSESTG00000028842 ENSESTT00000072775 Transcript intron_variant - - - - - - rs1510282 9:109703816 A ENSESTG00000028842 ENSESTT00000072765 Transcript intron_variant - - - - - - rs1510282 9:109703816 A ENSESTG00000028842 ENSESTT00000072755 Transcript downstream_gene_variant - - - - - - DISTANCE=2441 rs1510282 9:109703816 A ENSESTG00000028842 ENSESTT00000072724 Transcript intron_variant - - - - - - rs1510282 9:109703816 A ENSESTG00000028842 ENSESTT00000072706 Transcript intron_variant - - - - - - rs1510282 9:109703816 A CCDS35096.1 CCDS35096.1 Transcript intron_variant - - - - - - rs1510282 9:109703816 A 58499 NM_021224.4 Transcript intron_variant - - - - - - rs2259524 9:110342506 C - - - intergenic_variant - - - - - - rs10759259 9:110543628 C - - - intergenic_variant - - - - - - rs1855024 9:110980676 C - - - intergenic_variant - - - - - - rs559954 9:111142771 C - - - intergenic_variant - - - - - - rs838829 9:111723723 A ENSESTG00000030086 ENSESTT00000075883 Transcript intron_variant - - - - - - rs838829 9:111723723 A 8727 NM_003798.2 Transcript intron_variant - - - - - - rs838829 9:111723723 A CCDS6775.1 CCDS6775.1 Transcript intron_variant - - - - - - rs7043397 9:112097220 C - - - intergenic_variant - - - - - - rs7043365 9:112097480 G - - - intergenic_variant - - - - - - rs7023108 9:112288031 A ENSESTG00000029556 ENSESTT00000074597 Transcript intron_variant - - - - - - rs7023108 9:112288031 A ENSESTG00000029556 ENSESTT00000074599 Transcript intron_variant - - - - - - rs7023108 9:112288031 A ENSESTG00000029556 ENSESTT00000074630 Transcript intron_variant - - - - - - rs7023108 9:112288031 A ENSESTG00000029556 ENSESTT00000074626 Transcript intron_variant - - - - - - rs1752342 9:112637213 G CCDS35101.1 CCDS35101.1 Transcript intron_variant - - - - - - rs1752342 9:112637213 G ENSESTG00000034153 ENSESTT00000086336 Transcript intron_variant - - - - - - rs1752342 9:112637213 G CCDS35100.1 CCDS35100.1 Transcript intron_variant - - - - - - rs1752342 9:112637213 G CCDS48002.2 CCDS48002.2 Transcript intron_variant - - - - - - rs1752342 9:112637213 G 445815 NM_147150.2 Transcript intron_variant - - - - - - rs1752342 9:112637213 G 445815 NM_007203.4 Transcript intron_variant - - - - - - rs1752342 9:112637213 G 114299 NM_001037293.2 Transcript intron_variant - - - - - - rs1752342 9:112637213 G ENSESTG00000034153 ENSESTT00000086349 Transcript intron_variant - - - - - - rs1752342 9:112637213 G CCDS35099.1 CCDS35099.1 Transcript intron_variant - - - - - - rs1752342 9:112637213 G 114299 NM_053016.5 Transcript intron_variant - - - - - - rs1752342 9:112637213 G ENSESTG00000034153 ENSESTT00000086331 Transcript intron_variant - - - - - - rs7031793 9:113273896 T ENSESTG00000034177 ENSESTT00000086434 Transcript intron_variant - - - - - - rs7031793 9:113273896 T ENSESTG00000034177 ENSESTT00000086440 Transcript downstream_gene_variant - - - - - - DISTANCE=1448 rs7031793 9:113273896 T ENSESTG00000034177 ENSESTT00000086403 Transcript downstream_gene_variant - - - - - - DISTANCE=1415 rs7031793 9:113273896 T CCDS48004.1 CCDS48004.1 Transcript intron_variant - - - - - - rs7031793 9:113273896 T 79987 NM_153366.3 Transcript intron_variant - - - - - - rs2110544 9:113854330 A - - - intergenic_variant - - - - - - rs1008612 9:113858839 T - - - intergenic_variant - - - - - - rs2418133 9:113860844 A - - - intergenic_variant - - - - - - rs10733585 9:114977393 A 9991 NM_001163790.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2602 rs10733585 9:114977393 A 9991 NM_001244898.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2602 rs10733585 9:114977393 A 9991 NM_001244896.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2602 rs10733585 9:114977393 A 9991 NM_001244897.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2602 rs10733585 9:114977393 A 9991 NM_001163788.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2602 rs10733585 9:114977393 A 9991 NM_005156.6 Transcript downstream_gene_variant - - - - - - DISTANCE=2602 rs7867831 9:115142507 G - ENSR00001311831 RegulatoryFeature regulatory_region_variant - - - - - - rs7867831 9:115142507 G ENSESTG00000012259 ENSESTT00000030764 Transcript intron_variant - - - - - - rs7867831 9:115142507 G CCDS56582.1 CCDS56582.1 Transcript intron_variant - - - - - - rs7867831 9:115142507 G ENSESTG00000012259 ENSESTT00000030779 Transcript intron_variant - - - - - - rs7867831 9:115142507 G 84263 NR_036651.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7867831 9:115142507 G 84263 NM_001195822.1 Transcript intron_variant - - - - - - rs7867831 9:115142507 G ENSESTG00000012259 ENSESTT00000030757 Transcript intron_variant - - - - - - rs7867831 9:115142507 G CCDS43864.1 CCDS43864.1 Transcript intron_variant - - - - - - rs7867831 9:115142507 G ENSESTG00000012259 ENSESTT00000030752 Transcript intron_variant - - - - - - rs7867831 9:115142507 G 84263 NM_032303.4 Transcript intron_variant - - - - - - rs1886130 9:116774088 G ENSESTG00000030925 ENSESTT00000077965 Transcript downstream_gene_variant - - - - - - DISTANCE=3289 rs1886130 9:116774088 G ENSESTG00000030925 ENSESTT00000077942 Transcript intron_variant - - - - - - rs1886130 9:116774088 G ENSESTG00000030925 ENSESTT00000078000 Transcript upstream_gene_variant - - - - - - DISTANCE=4913 rs1886130 9:116774088 G 114991 NM_133374.2 Transcript intron_variant - - - - - - rs1886130 9:116774088 G CCDS48008.1 CCDS48008.1 Transcript intron_variant - - - - - - rs7871043 9:116878603 G - - - intergenic_variant - - - - - - rs2104146 9:117583801 T - - - intergenic_variant - - - - - - rs10817697 9:117758040 G - - - intergenic_variant - - - - - - rs849036 9:118077064 C 50514 NM_017418.2 Transcript intron_variant - - - - - - rs849036 9:118077064 C ENSESTG00000001632 ENSESTT00000003931 Transcript intron_variant - - - - - - rs4979519 9:118107933 T 50514 NM_017418.2 Transcript intron_variant - - - - - - rs4551440 9:118284488 C - - - intergenic_variant - - - - - - rs7026128 9:118405875 A - - - intergenic_variant - - - - - - rs7468667 9:118425710 G - - - intergenic_variant - - - - - - rs6478216 9:118709946 C - - - intergenic_variant - - - - - - rs7872586 9:118752056 G - - - intergenic_variant - - - - - - rs6415823 9:118780826 T - - - intergenic_variant - - - - - - rs4978659 9:118858906 C - - - intergenic_variant - - - - - - rs449737 9:119000964 G - ENSR00001312679 RegulatoryFeature regulatory_region_variant - - - - - - rs449737 9:119000964 G CCDS6813.1 CCDS6813.1 Transcript intron_variant - - - - - - rs449737 9:119000964 G ENSESTG00000022266 ENSESTT00000056418 Transcript intron_variant - - - - - - rs449737 9:119000964 G ENSESTG00000022266 ENSESTT00000056408 Transcript intron_variant - - - - - - rs449737 9:119000964 G 5069 NM_002581.3 Transcript intron_variant - - - - - - rs7024360 9:119283835 T 100128505 NR_033973.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7024360 9:119283835 T 23245 NM_014010.4 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022791 ENSESTT00000057713 Transcript intron_variant - - - - - - rs7024360 9:119283835 T 23245 NM_198187.3 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022791 ENSESTT00000057632 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022791 ENSESTT00000057722 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022791 ENSESTT00000057643 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022579 ENSESTT00000056991 Transcript intron_variant - - - - - - rs7024360 9:119283835 T CCDS48009.2 CCDS48009.2 Transcript intron_variant - - - - - - rs7024360 9:119283835 T 23245 NM_001184734.1 Transcript intron_variant - - - - - - rs7024360 9:119283835 T 23245 NM_198188.2 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022579 ENSESTT00000057009 Transcript intron_variant - - - - - - rs7024360 9:119283835 T CCDS6814.1 CCDS6814.1 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022791 ENSESTT00000057651 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022791 ENSESTT00000057702 Transcript intron_variant - - - - - - rs7024360 9:119283835 T 23245 NM_198186.3 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022791 ENSESTT00000057701 Transcript intron_variant - - - - - - rs7024360 9:119283835 T CCDS6815.1 CCDS6815.1 Transcript intron_variant - - - - - - rs7024360 9:119283835 T ENSESTG00000022791 ENSESTT00000057695 Transcript intron_variant - - - - - - rs894209 9:119497694 C 23245 NM_014010.4 Transcript intron_variant - - - - - - rs894209 9:119497694 C ENSESTG00000026071 ENSESTT00000065951 Transcript intron_variant - - - - - - rs894209 9:119497694 C ENSESTG00000026071 ENSESTT00000065903 Transcript intron_variant - - - - - - rs894209 9:119497694 C CCDS6815.1 CCDS6815.1 Transcript intron_variant - - - - - - rs894209 9:119497694 C ENSESTG00000026071 ENSESTT00000065895 Transcript intron_variant - - - - - - rs7029512 9:120226621 A - - - intergenic_variant - - - - - - rs575352 9:120269762 G - - - intergenic_variant - - - - - - rs2780233 9:120763221 T ENSESTG00000029093 ENSESTT00000073279 Transcript intron_variant - - - - - - rs2780233 9:120763221 T ENSESTG00000029093 ENSESTT00000073247 Transcript intron_variant - - - - - - rs2780233 9:120763221 T ENSESTG00000029093 ENSESTT00000073307 Transcript intron_variant - - - - - - rs6478360 9:121214225 T - - - intergenic_variant - - - - - - rs10126031 9:121699399 T - - - intergenic_variant - - - - - - rs10732387 9:121822192 C - - - intergenic_variant - - - - - - rs7048008 9:122119938 T 1620 NM_014618.2 Transcript intron_variant - - - - - - rs7048008 9:122119938 T ENSESTG00000013054 ENSESTT00000032772 Transcript intron_variant - - - - - - rs7048008 9:122119938 T ENSESTG00000013054 ENSESTT00000032774 Transcript intron_variant - - - - - - rs7048008 9:122119938 T ENSESTG00000013054 ENSESTT00000032775 Transcript intron_variant - - - - - - rs7048008 9:122119938 T ENSESTG00000013054 ENSESTT00000032761 Transcript intron_variant - - - - - - rs7048008 9:122119938 T ENSESTG00000013054 ENSESTT00000032768 Transcript intron_variant - - - - - - rs1333925 9:122699209 T - - - intergenic_variant - - - - - - rs2416796 9:123462920 A ENSESTG00000021295 ENSESTT00000053557 Transcript intron_variant - - - - - - rs2416796 9:123462920 A ENSESTG00000021295 ENSESTT00000053550 Transcript intron_variant - - - - - - rs2416796 9:123462920 A ENSESTG00000021295 ENSESTT00000053541 Transcript intron_variant - - - - - - rs2416796 9:123462920 A CCDS48010.2 CCDS48010.2 Transcript intron_variant - - - - - - rs2416796 9:123462920 A 1955 NM_001080497.2 Transcript intron_variant - - - - - - rs4837824 9:124015079 C - - - intergenic_variant - - - - - - rs1034083 9:124032867 T ENSESTG00000019924 ENSESTT00000050060 Transcript intron_variant - - - - - - rs1034083 9:124032867 T ENSESTG00000019924 ENSESTT00000050047 Transcript intron_variant - - - - - - rs1034083 9:124032867 T ENSESTG00000019924 ENSESTT00000050071 Transcript intron_variant - - - - - - rs1034083 9:124032867 T ENSESTG00000019924 ENSESTT00000050016 Transcript intron_variant - - - - - - rs1034083 9:124032867 T ENSESTG00000019924 ENSESTT00000050105 Transcript intron_variant - - - - - - rs1034083 9:124032867 T 2934 NM_001127662.1 Transcript intron_variant - - - - - - rs1034083 9:124032867 T ENSESTG00000019924 ENSESTT00000049987 Transcript intron_variant - - - - - - rs1034083 9:124032867 T 2934 NM_001127665.1 Transcript intron_variant - - - - - - rs1034083 9:124032867 T ENSESTG00000019924 ENSESTT00000050094 Transcript intron_variant - - - - - - rs1034083 9:124032867 T 2934 NM_198252.2 Transcript intron_variant - - - - - - rs1034083 9:124032867 T 2934 NM_001127666.1 Transcript intron_variant - - - - - - rs1034083 9:124032867 T 2934 NM_001127663.1 Transcript intron_variant - - - - - - rs1034083 9:124032867 T 2934 NM_001127667.1 Transcript intron_variant - - - - - - rs1034083 9:124032867 T 2934 NM_001127664.1 Transcript intron_variant - - - - - - rs7031882 9:124432853 C - ENSR00001474777 RegulatoryFeature regulatory_region_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021034 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021043 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021022 Transcript intron_variant - - - - - - rs7031882 9:124432853 C CCDS6833.2 CCDS6833.2 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021040 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021001 Transcript intron_variant - - - - - - rs7031882 9:124432853 C 153090 NM_032552.2 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021060 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021008 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021055 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000020982 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021006 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021015 Transcript intron_variant - - - - - - rs7031882 9:124432853 C ENSESTG00000008292 ENSESTT00000021030 Transcript intron_variant - - - - - - rs4837916 9:124685561 G CCDS48012.1 CCDS48012.1 Transcript intron_variant - - - - - - rs4837916 9:124685561 G ENSESTG00000008592 ENSESTT00000021600 Transcript intron_variant - - - - - - rs4837916 9:124685561 G ENSESTG00000008599 ENSESTT00000021610 Transcript intron_variant - - - - - - rs4837916 9:124685561 G 158135 NM_001139442.1 Transcript intron_variant - - - - - - rs7869722 9:124946099 A ENSESTG00000008392 ENSESTT00000021171 Transcript intron_variant - - - - - - rs7869722 9:124946099 A 254956 NM_198469.2 Transcript intron_variant - - - - - - rs7869722 9:124946099 A CCDS6836.1 CCDS6836.1 Transcript intron_variant - - - - - - rs2058374 9:125515458 T 392390 NM_001004453.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2396 rs2058374 9:125515458 T CCDS35130.2 CCDS35130.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2396 rs2058374 9:125515458 T ENSESTG00000018773 ENSESTT00000047299 Transcript intron_variant - - - - - - rs4836947 9:126733895 C - - - intergenic_variant - - - - - - rs6478663 9:127172880 A - ENSR00001474979 RegulatoryFeature regulatory_region_variant - - - - - - rs6478663 9:127172880 A CCDS6855.1 CCDS6855.1 Transcript intron_variant - - - - - - rs6478663 9:127172880 A 5695 NM_002799.3 Transcript intron_variant - - - - - - rs6478663 9:127172880 A ENSESTG00000025840 ENSESTT00000065280 Transcript intron_variant - - - - - - rs7864593 9:128201098 G 79109 NM_024117.3 Transcript 3_prime_UTR_variant 1862 - - - - - rs7864593 9:128201098 G ENSESTG00000025429 ENSESTT00000064327 Transcript 3_prime_UTR_variant 1308 - - - - - rs7864593 9:128201098 G CCDS35139.1 CCDS35139.1 Transcript downstream_gene_variant - - - - - - DISTANCE=68 rs7864593 9:128201098 G CCDS35141.1 CCDS35141.1 Transcript downstream_gene_variant - - - - - - DISTANCE=68 rs7864593 9:128201098 G 79109 NM_001006621.1 Transcript 3_prime_UTR_variant 1552 - - - - - rs7864593 9:128201098 G ENSESTG00000025429 ENSESTT00000064339 Transcript 3_prime_UTR_variant 936 - - - - - rs7864593 9:128201098 G ENSESTG00000025429 ENSESTT00000064413 Transcript 3_prime_UTR_variant 654 - - - - - rs7864593 9:128201098 G 79109 NM_001006619.1 Transcript 3_prime_UTR_variant 1829 - - - - - rs7864593 9:128201098 G CCDS6864.1 CCDS6864.1 Transcript downstream_gene_variant - - - - - - DISTANCE=68 rs7864593 9:128201098 G 79109 NM_001006620.1 Transcript 3_prime_UTR_variant 1642 - - - - - rs7864593 9:128201098 G 79109 NM_001006617.1 Transcript 3_prime_UTR_variant 1970 - - - - - rs7864593 9:128201098 G ENSESTG00000025429 ENSESTT00000064263 Transcript 3_prime_UTR_variant 985 - - - - - rs7864593 9:128201098 G CCDS35140.1 CCDS35140.1 Transcript downstream_gene_variant - - - - - - DISTANCE=68 rs7864593 9:128201098 G ENSESTG00000025429 ENSESTT00000064435 Transcript 5_prime_UTR_variant 335 - - - - - rs499864 9:128290417 G 79109 NM_024117.3 Transcript intron_variant - - - - - - rs499864 9:128290417 G ENSESTG00000025429 ENSESTT00000064402 Transcript intron_variant - - - - - - rs499864 9:128290417 G ENSESTG00000025429 ENSESTT00000064327 Transcript intron_variant - - - - - - rs499864 9:128290417 G CCDS48020.1 CCDS48020.1 Transcript intron_variant - - - - - - rs499864 9:128290417 G 79109 NM_001006618.1 Transcript intron_variant - - - - - - rs499864 9:128290417 G CCDS35139.1 CCDS35139.1 Transcript intron_variant - - - - - - rs499864 9:128290417 G CCDS35141.1 CCDS35141.1 Transcript intron_variant - - - - - - rs499864 9:128290417 G ENSESTG00000025429 ENSESTT00000064339 Transcript intron_variant - - - - - - rs499864 9:128290417 G 79109 NM_001006621.1 Transcript intron_variant - - - - - - rs499864 9:128290417 G 79109 NM_001006619.1 Transcript intron_variant - - - - - - rs499864 9:128290417 G CCDS6864.1 CCDS6864.1 Transcript intron_variant - - - - - - rs499864 9:128290417 G 79109 NM_001006620.1 Transcript intron_variant - - - - - - rs499864 9:128290417 G 79109 NM_001006617.1 Transcript intron_variant - - - - - - rs499864 9:128290417 G ENSESTG00000025429 ENSESTT00000064263 Transcript intron_variant - - - - - - rs499864 9:128290417 G CCDS35140.1 CCDS35140.1 Transcript intron_variant - - - - - - rs10760402 9:128545187 A ENSESTG00000026600 ENSESTT00000067166 Transcript intron_variant - - - - - - rs10760402 9:128545187 A CCDS48021.1 CCDS48021.1 Transcript intron_variant - - - - - - rs10760402 9:128545187 A 5090 NR_024123.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10760402 9:128545187 A ENSESTG00000026600 ENSESTT00000067148 Transcript intron_variant - - - - - - rs10760402 9:128545187 A 5090 NR_024122.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs10760402 9:128545187 A 5090 NM_001134778.1 Transcript intron_variant - - - - - - rs10760402 9:128545187 A CCDS6865.1 CCDS6865.1 Transcript intron_variant - - - - - - rs10760402 9:128545187 A 5090 NM_006195.5 Transcript intron_variant - - - - - - rs10760402 9:128545187 A ENSESTG00000026600 ENSESTT00000067024 Transcript intron_variant - - - - - - rs1558837 9:128833805 C - - - intergenic_variant - - - - - - rs7389704 9:128834467 C - - - intergenic_variant - - - - - - rs2809432 9:129022798 G - - - intergenic_variant - - - - - - rs3861876 9:129442836 G 4010 NM_002316.3 Transcript intron_variant - - - - - - rs3861876 9:129442836 G ENSESTG00000012677 ENSESTT00000031829 Transcript intron_variant - - - - - - rs3861876 9:129442836 G CCDS55343.1 CCDS55343.1 Transcript intron_variant - - - - - - rs3861876 9:129442836 G CCDS55342.1 CCDS55342.1 Transcript intron_variant - - - - - - rs3861876 9:129442836 G 4010 NM_001174146.1 Transcript intron_variant - - - - - - rs3861876 9:129442836 G 4010 NM_001174147.1 Transcript intron_variant - - - - - - rs3861876 9:129442836 G CCDS6866.2 CCDS6866.2 Transcript intron_variant - - - - - - rs1566210 9:129631850 T - ENSR00001475159 RegulatoryFeature regulatory_region_variant - - - - - - rs1566210 9:129631850 T 403341 NM_001099270.1 Transcript intron_variant - - - - - - rs617793 9:129672160 G 9649 NM_001190730.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4893 rs617793 9:129672160 G 9649 NM_001190729.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4893 rs617793 9:129672160 G ENSESTG00000012719 ENSESTT00000031972 Transcript upstream_gene_variant - - - - - - DISTANCE=4986 rs617793 9:129672160 G ENSESTG00000012719 ENSESTT00000031968 Transcript upstream_gene_variant - - - - - - DISTANCE=4940 rs617793 9:129672160 G 9649 NM_014636.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4893 rs1281158 9:129831659 A 9649 NM_001190729.1 Transcript intron_variant - - - - - - rs1281158 9:129831659 A CCDS35143.1 CCDS35143.1 Transcript intron_variant - - - - - - rs1281158 9:129831659 A 9649 NM_001190728.1 Transcript intron_variant - - - - - - rs1281158 9:129831659 A CCDS55346.1 CCDS55346.1 Transcript intron_variant - - - - - - rs1281158 9:129831659 A ENSESTG00000012719 ENSESTT00000031983 Transcript intron_variant - - - - - - rs1281158 9:129831659 A 9649 NM_001190730.1 Transcript intron_variant - - - - - - rs1281158 9:129831659 A CCDS55344.1 CCDS55344.1 Transcript intron_variant - - - - - - rs1281158 9:129831659 A CCDS55345.1 CCDS55345.1 Transcript intron_variant - - - - - - rs1281158 9:129831659 A ENSESTG00000012719 ENSESTT00000031968 Transcript intron_variant - - - - - - rs1281158 9:129831659 A 9649 NM_014636.2 Transcript intron_variant - - - - - - rs1281162 9:129901528 C 9649 NM_001190729.1 Transcript intron_variant - - - - - - rs1281162 9:129901528 C CCDS35143.1 CCDS35143.1 Transcript intron_variant - - - - - - rs1281162 9:129901528 C 9649 NM_001190728.1 Transcript intron_variant - - - - - - rs1281162 9:129901528 C CCDS55346.1 CCDS55346.1 Transcript intron_variant - - - - - - rs1281162 9:129901528 C ENSESTG00000012719 ENSESTT00000031983 Transcript intron_variant - - - - - - rs1281162 9:129901528 C 9649 NM_001190730.1 Transcript intron_variant - - - - - - rs1281162 9:129901528 C CCDS55344.1 CCDS55344.1 Transcript intron_variant - - - - - - rs1281162 9:129901528 C CCDS55345.1 CCDS55345.1 Transcript intron_variant - - - - - - rs1281162 9:129901528 C ENSESTG00000012719 ENSESTT00000031968 Transcript intron_variant - - - - - - rs1281162 9:129901528 C 9649 NM_014636.2 Transcript intron_variant - - - - - - rs4837191 9:130610828 A 2022 NM_001114753.1 Transcript intron_variant - - - - - - rs4837191 9:130610828 A ENSESTG00000034822 ENSESTT00000088064 Transcript upstream_gene_variant - - - - - - DISTANCE=1410 rs4837191 9:130610828 A ENSESTG00000034822 ENSESTT00000088068 Transcript upstream_gene_variant - - - - - - DISTANCE=1413 rs4837191 9:130610828 A CCDS48029.1 CCDS48029.1 Transcript intron_variant - - - - - - rs4837191 9:130610828 A ENSESTG00000034822 ENSESTT00000088048 Transcript intron_variant - - - - - - rs4837191 9:130610828 A ENSESTG00000034822 ENSESTT00000088053 Transcript upstream_gene_variant - - - - - - DISTANCE=1391 rs4837191 9:130610828 A ENSESTG00000034822 ENSESTT00000088063 Transcript upstream_gene_variant - - - - - - DISTANCE=1410 rs4837191 9:130610828 A 2022 NM_000118.2 Transcript intron_variant - - - - - - rs4837191 9:130610828 A CCDS6880.1 CCDS6880.1 Transcript intron_variant - - - - - - rs1220802 9:132204555 G - ENSR00001315447 RegulatoryFeature regulatory_region_variant - - - - - - rs1220802 9:132204555 G ENSESTG00000025005 ENSESTT00000063092 Transcript downstream_gene_variant - - - - - - DISTANCE=4356 rs7855720 9:132672319 A ENSESTG00000020283 ENSESTT00000051160 Transcript intron_variant - - - - - - rs7855720 9:132672319 A ENSESTG00000020283 ENSESTT00000051043 Transcript intron_variant - - - - - - rs7855720 9:132672319 A ENSESTG00000020283 ENSESTT00000051177 Transcript intron_variant - - - - - - rs7855720 9:132672319 A 23048 NM_015033.2 Transcript intron_variant - - - - - - rs7855720 9:132672319 A ENSESTG00000020283 ENSESTT00000051236 Transcript intron_variant - - - - - - rs7855720 9:132672319 A CCDS48040.1 CCDS48040.1 Transcript intron_variant - - - - - - rs7855720 9:132672319 A ENSESTG00000020283 ENSESTT00000051252 Transcript upstream_gene_variant - - - - - - DISTANCE=1088 rs7855720 9:132672319 A ENSESTG00000020283 ENSESTT00000051021 Transcript intron_variant - - - - - - rs7855720 9:132672319 A ENSESTG00000020283 ENSESTT00000051224 Transcript intron_variant - - - - - - rs7043605 9:132737055 C ENSESTG00000020283 ENSESTT00000051160 Transcript intron_variant - - - - - - rs7043605 9:132737055 C ENSESTG00000020283 ENSESTT00000051066 Transcript intron_variant - - - - - - rs7043605 9:132737055 C ENSESTG00000020283 ENSESTT00000051043 Transcript intron_variant - - - - - - rs7043605 9:132737055 C ENSESTG00000020283 ENSESTT00000051190 Transcript intron_variant - - - - - - rs7043605 9:132737055 C ENSESTG00000020283 ENSESTT00000051177 Transcript intron_variant - - - - - - rs7043605 9:132737055 C 23048 NM_015033.2 Transcript intron_variant - - - - - - rs7043605 9:132737055 C CCDS48040.1 CCDS48040.1 Transcript intron_variant - - - - - - rs7043605 9:132737055 C ENSESTG00000020283 ENSESTT00000051021 Transcript intron_variant - - - - - - rs10733706 9:132742883 C ENSESTG00000020283 ENSESTT00000051160 Transcript intron_variant - - - - - - rs10733706 9:132742883 C ENSESTG00000020283 ENSESTT00000051066 Transcript intron_variant - - - - - - rs10733706 9:132742883 C ENSESTG00000020283 ENSESTT00000051043 Transcript intron_variant - - - - - - rs10733706 9:132742883 C ENSESTG00000020283 ENSESTT00000051190 Transcript intron_variant - - - - - - rs10733706 9:132742883 C ENSESTG00000020283 ENSESTT00000051177 Transcript intron_variant - - - - - - rs10733706 9:132742883 C 23048 NM_015033.2 Transcript intron_variant - - - - - - rs10733706 9:132742883 C CCDS48040.1 CCDS48040.1 Transcript intron_variant - - - - - - rs10733706 9:132742883 C ENSESTG00000020283 ENSESTT00000051021 Transcript intron_variant - - - - - - rs605448 9:132799846 C ENSESTG00000020283 ENSESTT00000051160 Transcript intron_variant - - - - - - rs605448 9:132799846 C ENSESTG00000020283 ENSESTT00000051066 Transcript intron_variant - - - - - - rs605448 9:132799846 C ENSESTG00000020283 ENSESTT00000051043 Transcript intron_variant - - - - - - rs605448 9:132799846 C ENSESTG00000020283 ENSESTT00000051190 Transcript intron_variant - - - - - - rs605448 9:132799846 C ENSESTG00000020283 ENSESTT00000051177 Transcript intron_variant - - - - - - rs605448 9:132799846 C 23048 NM_015033.2 Transcript intron_variant - - - - - - rs605448 9:132799846 C CCDS48040.1 CCDS48040.1 Transcript intron_variant - - - - - - rs605448 9:132799846 C ENSESTG00000020283 ENSESTT00000051021 Transcript intron_variant - - - - - - rs1557127 9:132952231 C - ENSR00001475419 RegulatoryFeature regulatory_region_variant - - - - - - rs1557127 9:132952231 C CCDS6932.1 CCDS6932.1 Transcript intron_variant - - - - - - rs1557127 9:132952231 C ENSESTG00000020138 ENSESTT00000050531 Transcript upstream_gene_variant - - - - - - DISTANCE=3521 rs1557127 9:132952231 C 23413 NM_014286.3 Transcript intron_variant - - - - - - rs6597641 9:133270740 C - ENSR00001315785 RegulatoryFeature regulatory_region_variant - - - - - - rs6597641 9:133270740 C 256158 XM_001726942.3 Transcript splice_region_variant,intron_variant - - - - - - rs6597641 9:133270740 C ENSESTG00000029986 ENSESTT00000075455 Transcript upstream_gene_variant - - - - - - DISTANCE=3226 rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076952 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076965 Transcript 5_prime_UTR_variant 168 - - - - - rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076973 Transcript upstream_gene_variant - - - - - - DISTANCE=2563 rs353526 9:133986980 G 83543 NM_001185095.1 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076928 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076979 Transcript upstream_gene_variant - - - - - - DISTANCE=2661 rs353526 9:133986980 G 83543 NM_031426.3 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076879 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076946 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G CCDS6939.1 CCDS6939.1 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G CCDS55348.1 CCDS55348.1 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G 83543 NM_001185096.1 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G 83543 NR_033701.1 Transcript splice_region_variant,intron_variant,nc_transcript_variant - - - - - - rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076908 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076885 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G CCDS55349.1 CCDS55349.1 Transcript splice_region_variant,intron_variant - - - - - - rs353526 9:133986980 G ENSESTG00000030468 ENSESTT00000076845 Transcript splice_region_variant,intron_variant - - - - - - rs3012751 9:134663784 A - - - intergenic_variant - - - - - - rs2987363 9:134670908 G - - - intergenic_variant - - - - - - rs9328535 9:134881208 G CCDS59153.1 CCDS59153.1 Transcript intron_variant - - - - - - rs9328535 9:134881208 G 9442 NM_001253881.1 Transcript intron_variant - - - - - - rs9328535 9:134881208 G ENSESTG00000031158 ENSESTT00000078605 Transcript intron_variant - - - - - - rs9328535 9:134881208 G CCDS6945.1 CCDS6945.1 Transcript intron_variant - - - - - - rs9328535 9:134881208 G 9442 NM_004269.3 Transcript intron_variant - - - - - - rs572712 9:135258709 C CCDS6948.1 CCDS6948.1 Transcript intron_variant - - - - - - rs572712 9:135258709 C 7270 NM_007344.3 Transcript intron_variant - - - - - - rs572712 9:135258709 C ENSESTG00000002664 ENSESTT00000006656 Transcript intron_variant - - - - - - rs572712 9:135258709 C 7270 NM_001205296.1 Transcript intron_variant - - - - - - rs2583798 9:135511467 C 64794 NM_022779.7 Transcript intron_variant - - - - - - rs2583798 9:135511467 C CCDS6951.1 CCDS6951.1 Transcript intron_variant - - - - - - rs2583798 9:135511467 C ENSESTG00000002648 ENSESTT00000006599 Transcript intron_variant - - - - - - rs2583798 9:135511467 C 64794 NM_138620.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1783 rs2583798 9:135511467 C CCDS6952.1 CCDS6952.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2281 rs2583798 9:135511467 C ENSESTG00000002648 ENSESTT00000006628 Transcript intron_variant - - - - - - rs2519756 9:135751094 T ENSESTG00000002378 ENSESTT00000005949 Transcript upstream_gene_variant - - - - - - DISTANCE=3230 rs2519756 9:135751094 T ENSESTG00000002378 ENSESTT00000005931 Transcript upstream_gene_variant - - - - - - DISTANCE=2613 rs2519756 9:135751094 T ENSESTG00000002378 ENSESTT00000005945 Transcript upstream_gene_variant - - - - - - DISTANCE=3196 rs2519756 9:135751094 T ENSESTG00000002378 ENSESTT00000005921 Transcript upstream_gene_variant - - - - - - DISTANCE=2010 rs2519756 9:135751094 T ENSESTG00000002378 ENSESTT00000005914 Transcript upstream_gene_variant - - - - - - DISTANCE=2010 rs2519756 9:135751094 T CCDS6954.1 CCDS6954.1 Transcript intron_variant - - - - - - rs2519756 9:135751094 T ENSESTG00000002632 ENSESTT00000006537 Transcript intron_variant - - - - - - rs2519756 9:135751094 T ENSESTG00000002378 ENSESTT00000005947 Transcript upstream_gene_variant - - - - - - DISTANCE=3219 rs2519756 9:135751094 T ENSESTG00000002632 ENSESTT00000006543 Transcript intron_variant - - - - - - rs2519756 9:135751094 T ENSESTG00000002632 ENSESTT00000006548 Transcript intron_variant - - - - - - rs2519756 9:135751094 T 11092 NM_018956.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3196 rs2519756 9:135751094 T 158067 NM_152572.2 Transcript intron_variant - - - - - - rs2519756 9:135751094 T ENSESTG00000002378 ENSESTT00000005935 Transcript upstream_gene_variant - - - - - - DISTANCE=2616 rs2519756 9:135751094 T ENSESTG00000002378 ENSESTT00000005910 Transcript upstream_gene_variant - - - - - - DISTANCE=2010 rs2519756 9:135751094 T ENSESTG00000002378 ENSESTT00000005933 Transcript upstream_gene_variant - - - - - - DISTANCE=2613 rs2519756 9:135751094 T ENSESTG00000002632 ENSESTT00000006550 Transcript intron_variant - - - - - - rs10736858 9:135790261 A CCDS55350.1 CCDS55350.1 Transcript intron_variant - - - - - - rs10736858 9:135790261 A 7248 NM_001162427.1 Transcript intron_variant - - - - - - rs10736858 9:135790261 A 7248 NM_000368.4 Transcript intron_variant - - - - - - rs10736858 9:135790261 A CCDS6956.1 CCDS6956.1 Transcript intron_variant - - - - - - rs10736858 9:135790261 A 7248 NM_001162426.1 Transcript intron_variant - - - - - - rs6597605 9:136052946 C - - - intergenic_variant - - - - - - rs1179033 9:136234124 G ENSESTG00000002544 ENSESTT00000006325 Transcript intron_variant - - - - - - rs1179033 9:136234124 G ENSESTG00000002544 ENSESTT00000006332 Transcript intron_variant - - - - - - rs1179033 9:136234124 G ENSESTG00000002544 ENSESTT00000006293 Transcript downstream_gene_variant - - - - - - DISTANCE=237 rs1179033 9:136234124 G ENSESTG00000002544 ENSESTT00000006312 Transcript intron_variant - - - - - - rs1179033 9:136234124 G CCDS6968.1 CCDS6968.1 Transcript intron_variant - - - - - - rs1179033 9:136234124 G 6836 NM_033161.2 Transcript intron_variant - - - - - - rs2519133 9:136840389 C CCDS48053.1 CCDS48053.1 Transcript intron_variant - - - - - - rs2519133 9:136840389 C ENSESTG00000001896 ENSESTT00000004733 Transcript intron_variant - - - - - - rs2519133 9:136840389 C ENSESTG00000001896 ENSESTT00000004739 Transcript intron_variant - - - - - - rs2519133 9:136840389 C 7410 NM_001134398.1 Transcript intron_variant - - - - - - rs2519133 9:136840389 C 7410 NM_003371.3 Transcript intron_variant - - - - - - rs2519133 9:136840389 C CCDS6979.1 CCDS6979.1 Transcript intron_variant - - - - - - rs28634919 9:137014321 A CCDS6981.1 CCDS6981.1 Transcript intron_variant - - - - - - rs28634919 9:137014321 A ENSESTG00000001837 ENSESTT00000004588 Transcript intron_variant - - - - - - rs28634919 9:137014321 A 11091 NM_017588.2 Transcript intron_variant - - - - - - rs28634919 9:137014321 A 11091 NM_052821.3 Transcript intron_variant - - - - - - rs3118544 9:137389010 G - ENSR00001317066 RegulatoryFeature regulatory_region_variant - - - - - - rs3118544 9:137389010 G - - - intergenic_variant - - - - - - rs3132308 9:137434583 A ENSESTG00000027240 ENSESTT00000068615 Transcript intron_variant - - - - - - rs10776869 9:137446676 G - ENSR00001475750 RegulatoryFeature regulatory_region_variant - - - - - - rs10776869 9:137446676 G ENSESTG00000027249 ENSESTT00000068633 Transcript downstream_gene_variant - - - - - - DISTANCE=933 rs3128577 9:137617195 C ENSESTG00000027282 ENSESTT00000068761 Transcript intron_variant - - - - - - rs3128577 9:137617195 C 1289 NM_000093.3 Transcript intron_variant - - - - - - rs3128577 9:137617195 C ENSESTG00000028126 ENSESTT00000070716 Transcript intron_variant - - - - - - rs3128577 9:137617195 C CCDS6982.1 CCDS6982.1 Transcript intron_variant - - - - - - rs10745391 9:137842662 G ENSESTG00000028025 ENSESTT00000070498 Transcript upstream_gene_variant - - - - - - DISTANCE=3488 rs540993 9:137950729 G - - - intergenic_variant - - - - - - rs1891990 9:138156664 A - - - intergenic_variant - - - - - - rs7045504 9:138290115 A - - - intergenic_variant - - - - - - rs697448 9:138453811 G - ENSR00001317288 RegulatoryFeature regulatory_region_variant - - - - - - rs697448 9:138453811 G 5047 NM_001018049.1 Transcript intron_variant - - - - - - rs697448 9:138453811 G 5047 NM_002571.2 Transcript intron_variant - - - - - - rs697448 9:138453811 G ENSESTG00000000125 ENSESTT00000000337 Transcript upstream_gene_variant - - - - - - DISTANCE=335 rs697448 9:138453811 G ENSESTG00000000125 ENSESTT00000000331 Transcript intron_variant - - - - - - rs697448 9:138453811 G ENSESTG00000000125 ENSESTT00000000341 Transcript upstream_gene_variant - - - - - - DISTANCE=2284 rs697448 9:138453811 G CCDS35173.1 CCDS35173.1 Transcript intron_variant - - - - - - rs697448 9:138453811 G ENSESTG00000000125 ENSESTT00000000325 Transcript intron_variant - - - - - - rs7854380 9:138856020 G 10422 NM_016172.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2794 rs7854380 9:138856020 G ENSESTG00000000234 ENSESTT00000000585 Transcript upstream_gene_variant - - - - - - DISTANCE=2845 rs7854380 9:138856020 G CCDS35177.1 CCDS35177.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3012 rs7029928 9:138951202 G - ENSR00001317435 RegulatoryFeature regulatory_region_variant - - - - - - rs7029928 9:138951202 G ENSESTG00000000225 ENSESTT00000000556 Transcript intron_variant - - - - - - rs7029928 9:138951202 G 138151 NM_144653.4 Transcript intron_variant - - - - - - rs10735244 9:138972914 A ENSESTG00000000225 ENSESTT00000000556 Transcript intron_variant - - - - - - rs10735244 9:138972914 A 138151 NM_144653.4 Transcript intron_variant - - - - - - rs1164897 9:139012281 C CCDS59155.1 CCDS59155.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3535 rs1164897 9:139012281 C 90120 NM_152833.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1550 rs1164897 9:139012281 C 90120 NM_001256526.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2004 rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000050382 Transcript downstream_gene_variant - - - - - - DISTANCE=4167 rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000050031 Transcript intron_variant - - - - - - rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000050350 Transcript downstream_gene_variant - - - - - - DISTANCE=2070 rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000050461 Transcript upstream_gene_variant - - - - - - DISTANCE=1368 rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000050418 Transcript intron_variant - - - - - - rs3124997 9:139343719 T 9919 NM_014866.1 Transcript intron_variant - - - - - - rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000050397 Transcript downstream_gene_variant - - - - - - DISTANCE=4167 rs3124997 9:139343719 T CCDS55351.1 CCDS55351.1 Transcript intron_variant - - - - - - rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000050446 Transcript upstream_gene_variant - - - - - - DISTANCE=1361 rs3124997 9:139343719 T ENSESTG00000016590 ENSESTT00000041597 Transcript intron_variant - - - - - - rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000050306 Transcript downstream_gene_variant - - - - - - DISTANCE=2070 rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000049806 Transcript intron_variant - - - - - - rs3124997 9:139343719 T ENSESTG00000019873 ENSESTT00000050501 Transcript upstream_gene_variant - - - - - - DISTANCE=2225 rs4880096 9:139356002 C ENSESTG00000019873 ENSESTT00000050382 Transcript intron_variant - - - - - - rs4880096 9:139356002 C ENSESTG00000019873 ENSESTT00000050031 Transcript intron_variant - - - - - - rs4880096 9:139356002 C ENSESTG00000019873 ENSESTT00000050350 Transcript intron_variant - - - - - - rs4880096 9:139356002 C 9919 NM_014866.1 Transcript intron_variant - - - - - - rs4880096 9:139356002 C ENSESTG00000019873 ENSESTT00000050397 Transcript intron_variant - - - - - - rs4880096 9:139356002 C CCDS55351.1 CCDS55351.1 Transcript intron_variant - - - - - - rs4880096 9:139356002 C ENSESTG00000019873 ENSESTT00000049806 Transcript intron_variant - - - - - - rs4880096 9:139356002 C ENSESTG00000019873 ENSESTT00000050306 Transcript intron_variant - - - - - - rs944756 9:139525963 C - ENSR00001317685 RegulatoryFeature regulatory_region_variant - - - - - - rs944756 9:139525963 C - - - intergenic_variant - - - - - - rs1547280 9:139541660 A ENSESTG00000019523 ENSESTT00000049003 Transcript downstream_gene_variant - - - - - - DISTANCE=1403 rs2026447 9:139577388 T 10555 NM_001012727.1 Transcript intron_variant - - - - - - rs2026447 9:139577388 T 10555 NM_006412.3 Transcript intron_variant - - - - - - rs2026447 9:139577388 T ENSESTG00000019412 ENSESTT00000048747 Transcript intron_variant - - - - - - rs2026447 9:139577388 T CCDS35181.1 CCDS35181.1 Transcript intron_variant - - - - - - rs2026447 9:139577388 T CCDS7003.1 CCDS7003.1 Transcript intron_variant - - - - - - rs1571985 9:139577687 A 10555 NM_001012727.1 Transcript intron_variant - - - - - - rs1571985 9:139577687 A 10555 NM_006412.3 Transcript intron_variant - - - - - - rs1571985 9:139577687 A ENSESTG00000019412 ENSESTT00000048747 Transcript intron_variant - - - - - - rs1571985 9:139577687 A CCDS35181.1 CCDS35181.1 Transcript intron_variant - - - - - - rs1571985 9:139577687 A CCDS7003.1 CCDS7003.1 Transcript intron_variant - - - - - - rs7019859 9:139584986 C 10555 NM_001012727.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3075 rs7019859 9:139584986 C 10555 NM_006412.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3075 rs7019859 9:139584986 C ENSESTG00000019412 ENSESTT00000048747 Transcript upstream_gene_variant - - - - - - DISTANCE=3190 rs7019859 9:139584986 C CCDS35181.1 CCDS35181.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3177 rs7019859 9:139584986 C CCDS7003.1 CCDS7003.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3177 rs7853539 9:139587632 G - ENSR00001317714 RegulatoryFeature regulatory_region_variant - - - - - - rs7853539 9:139587632 G - - - intergenic_variant - - - - - - rs4880131 9:139603152 C CCDS7004.1 CCDS7004.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3966 rs4880131 9:139603152 C 138311 NM_152421.3 Transcript upstream_gene_variant - - - - - - DISTANCE=3872 rs4880131 9:139603152 C ENSESTG00000016665 ENSESTT00000041815 Transcript upstream_gene_variant - - - - - - DISTANCE=3897 rs2784090 9:139717748 C - ENSR00001317773 RegulatoryFeature regulatory_region_variant - - - - - - rs2784090 9:139717748 C CCDS55352.1 CCDS55352.1 Transcript intron_variant - - - - - - rs2784090 9:139717748 C CCDS55353.1 CCDS55353.1 Transcript intron_variant - - - - - - rs2784090 9:139717748 C 55684 NM_001173989.2 Transcript intron_variant - - - - - - rs2784090 9:139717748 C ENSESTG00000016777 ENSESTT00000042152 Transcript upstream_gene_variant - - - - - - DISTANCE=300 rs2784090 9:139717748 C CCDS48058.1 CCDS48058.1 Transcript intron_variant - - - - - - rs2784090 9:139717748 C ENSESTG00000016777 ENSESTT00000042120 Transcript intron_variant - - - - - - rs2784090 9:139717748 C 55684 NM_024718.4 Transcript intron_variant - - - - - - rs2784090 9:139717748 C ENSESTG00000016777 ENSESTT00000042166 Transcript upstream_gene_variant - - - - - - DISTANCE=300 rs2784090 9:139717748 C 55684 NM_001173988.1 Transcript intron_variant - - - - - - rs2811745 9:139729748 C - ENSR00001317780 RegulatoryFeature regulatory_region_variant - - - - - - rs2811745 9:139729748 C CCDS55352.1 CCDS55352.1 Transcript intron_variant - - - - - - rs2811745 9:139729748 C 100422860 NR_036251.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4273 rs2811745 9:139729748 C ENSESTG00000019103 ENSESTT00000048049 Transcript downstream_gene_variant - - - - - - DISTANCE=3772 rs2811745 9:139729748 C CCDS55353.1 CCDS55353.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1337 rs2811745 9:139729748 C 55684 NM_001173989.2 Transcript downstream_gene_variant - - - - - - DISTANCE=820 rs2811745 9:139729748 C ENSESTG00000016777 ENSESTT00000042152 Transcript downstream_gene_variant - - - - - - DISTANCE=1065 rs2811745 9:139729748 C CCDS48058.1 CCDS48058.1 Transcript intron_variant - - - - - - rs2811745 9:139729748 C 55684 NM_024718.4 Transcript intron_variant - - - - - - rs2811745 9:139729748 C ENSESTG00000016817 ENSESTT00000042306 Transcript upstream_gene_variant - - - - - - DISTANCE=3944 rs2811745 9:139729748 C ENSESTG00000016803 ENSESTT00000042215 Transcript upstream_gene_variant - - - - - - DISTANCE=440 rs2811745 9:139729748 C 55684 NM_001173988.1 Transcript intron_variant - - - - - - rs1537795 9:139791684 C ENSESTG00000016956 ENSESTT00000042572 Transcript upstream_gene_variant - - - - - - DISTANCE=4712 rs1537795 9:139791684 C ENSESTG00000016956 ENSESTT00000042547 Transcript intron_variant - - - - - - rs1537795 9:139791684 C ENSESTG00000016956 ENSESTT00000042561 Transcript intron_variant - - - - - - rs1537795 9:139791684 C CCDS7013.1 CCDS7013.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1509 rs1537795 9:139791684 C 7186 NM_021138.3 Transcript intron_variant - - - - - - rs10870150 9:139854792 G ENSESTG00000017033 ENSESTT00000042858 Transcript downstream_gene_variant - - - - - - DISTANCE=4843 rs10870150 9:139854792 G CCDS7018.2 CCDS7018.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4941 rs10870150 9:139854792 G 286256 NM_178536.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4843 rs10870150 9:139854792 G ENSESTG00000018988 ENSESTT00000047755 Transcript upstream_gene_variant - - - - - - DISTANCE=4614 rs10870150 9:139854792 G ENSESTG00000017033 ENSESTT00000042833 Transcript downstream_gene_variant - - - - - - DISTANCE=4846 rs10870150 9:139854792 G ENSESTG00000017033 ENSESTT00000042801 Transcript downstream_gene_variant - - - - - - DISTANCE=4846 rs908838 9:139856551 G - - - intergenic_variant - - - - - - rs6560656 9:139900023 C CCDS43909.1 CCDS43909.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2358 rs6560656 9:139900023 C ENSESTG00000018872 ENSESTT00000047605 Transcript downstream_gene_variant - - - - - - DISTANCE=2273 rs6560656 9:139900023 C ENSESTG00000018872 ENSESTT00000047585 Transcript downstream_gene_variant - - - - - - DISTANCE=2280 rs6560656 9:139900023 C ENSESTG00000018864 ENSESTT00000047495 Transcript downstream_gene_variant - - - - - - DISTANCE=4033 rs6560656 9:139900023 C ENSESTG00000018872 ENSESTT00000047614 Transcript downstream_gene_variant - - - - - - DISTANCE=2086 rs6560656 9:139900023 C 20 NM_212533.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1663 rs6560656 9:139900023 C 20 NM_001606.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1663 rs908828 9:139913239 G ENSESTG00000018715 ENSESTT00000047246 Transcript downstream_gene_variant - - - - - - DISTANCE=3119 rs908828 9:139913239 G ENSESTG00000018851 ENSESTT00000047458 Transcript upstream_gene_variant - - - - - - DISTANCE=972 rs908828 9:139913239 G 20 NM_212533.2 Transcript missense_variant 1891 1841 614 H/P cAc/cCc - rs908828 9:139913239 G CCDS43909.1 CCDS43909.1 Transcript missense_variant 1751 1751 584 H/P cAc/cCc - PolyPhen=benign;SIFT=tolerated rs908828 9:139913239 G ENSESTG00000018715 ENSESTT00000047274 Transcript downstream_gene_variant - - - - - - DISTANCE=4419 rs908828 9:139913239 G ENSESTG00000018715 ENSESTT00000047178 Transcript downstream_gene_variant - - - - - - DISTANCE=3569 rs908828 9:139913239 G 20 NM_001606.4 Transcript missense_variant 1899 1751 584 H/P cAc/cCc - PolyPhen=benign;SIFT=tolerated rs908828 9:139913239 G ENSESTG00000018829 ENSESTT00000047410 Transcript missense_variant 806 623 208 H/P cAc/cCc - rs908828 9:139913239 G ENSESTG00000018829 ENSESTT00000047432 Transcript missense_variant 582 452 151 H/P cAc/cCc - rs9411297 9:139932568 C CCDS7023.1 CCDS7023.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3062 rs9411297 9:139932568 C ENSESTG00000017179 ENSESTT00000043149 Transcript downstream_gene_variant - - - - - - DISTANCE=2801 rs9411297 9:139932568 C ENSESTG00000018678 ENSESTT00000047082 Transcript downstream_gene_variant - - - - - - DISTANCE=1381 rs9411297 9:139932568 C ENSESTG00000018678 ENSESTT00000047130 Transcript intron_variant - - - - - - rs9411297 9:139932568 C ENSESTG00000017189 ENSESTT00000043159 Transcript upstream_gene_variant - - - - - - DISTANCE=2718 rs9411297 9:139932568 C 401563 NM_207511.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1334 rs9411297 9:139932568 C ENSESTG00000018678 ENSESTT00000047115 Transcript downstream_gene_variant - - - - - - DISTANCE=1348 rs9411297 9:139932568 C 56654 NM_015392.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1341 rs9411297 9:139932568 C CCDS7024.1 CCDS7024.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1656 rs9411297 9:139932568 C ENSESTG00000018678 ENSESTT00000047093 Transcript downstream_gene_variant - - - - - - DISTANCE=1381 rs7859283 9:140113179 T - ENSR00001317958 RegulatoryFeature regulatory_region_variant - - - - - - rs7859283 9:140113179 T ENSESTG00000017690 ENSESTT00000044563 Transcript upstream_gene_variant - - - - - - DISTANCE=1529 rs7859283 9:140113179 T 27158 NM_001144026.1 Transcript 3_prime_UTR_variant 4243 - - - - - rs7859283 9:140113179 T ENSESTG00000017685 ENSESTT00000044552 Transcript intron_variant - - - - - - rs7859283 9:140113179 T 27158 NM_001144027.1 Transcript 3_prime_UTR_variant 4092 - - - - - rs7859283 9:140113179 T ENSESTG00000018179 ENSESTT00000045773 Transcript intron_variant - - - - - - rs7859283 9:140113179 T CCDS48061.1 CCDS48061.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2311 rs7859283 9:140113179 T CCDS7037.2 CCDS7037.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1700 rs7859283 9:140113179 T 27158 NM_001144028.1 Transcript 3_prime_UTR_variant 4195 - - - - - rs7859283 9:140113179 T CCDS48062.1 CCDS48062.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2311 rs7859283 9:140113179 T CCDS48063.1 CCDS48063.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2415 rs7859283 9:140113179 T ENSESTG00000017428 ENSESTT00000043970 Transcript downstream_gene_variant - - - - - - DISTANCE=2318 rs7859283 9:140113179 T CCDS7036.1 CCDS7036.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2311 rs7859283 9:140113179 T 27158 NM_014434.2 Transcript 3_prime_UTR_variant 4216 - - - - - rs7859283 9:140113179 T 727800 NM_031297.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1520 rs7859283 9:140113179 T ENSESTG00000017428 ENSESTT00000043988 Transcript downstream_gene_variant - - - - - - DISTANCE=3833 rs6606573 9:140184203 G - - - intergenic_variant - - - - - - rs1891630 9:140374861 G ENSESTG00000031853 ENSESTT00000080492 Transcript downstream_gene_variant - - - - - - DISTANCE=571 rs1891630 9:140374861 G CCDS48070.1 CCDS48070.1 Transcript missense_variant 2483 2483 828 V/A gTa/gCa - PolyPhen=benign;SIFT=tolerated rs1891630 9:140374861 G 375775 NM_152286.3 Transcript missense_variant 2745 2408 803 V/A gTa/gCa - PolyPhen=benign;SIFT=tolerated rs1891630 9:140374861 G ENSESTG00000031853 ENSESTT00000080410 Transcript downstream_gene_variant - - - - - - DISTANCE=4234 rs1891630 9:140374861 G ENSESTG00000031853 ENSESTT00000080482 Transcript downstream_gene_variant - - - - - - DISTANCE=4249 rs1891630 9:140374861 G ENSESTG00000031909 ENSESTT00000080570 Transcript upstream_gene_variant - - - - - - DISTANCE=2258 rs1891630 9:140374861 G ENSESTG00000031853 ENSESTT00000080510 Transcript downstream_gene_variant - - - - - - DISTANCE=24 rs1891630 9:140374861 G ENSESTG00000031909 ENSESTT00000080579 Transcript upstream_gene_variant - - - - - - DISTANCE=2337 rs1891630 9:140374861 G ENSESTG00000031853 ENSESTT00000080464 Transcript downstream_gene_variant - - - - - - DISTANCE=574 rs1891630 9:140374861 G CCDS7045.1 CCDS7045.1 Transcript missense_variant 2408 2408 803 V/A gTa/gCa - PolyPhen=benign;SIFT=tolerated rs1891630 9:140374861 G 375775 NM_001098537.1 Transcript missense_variant 2820 2483 828 V/A gTa/gCa - PolyPhen=benign;SIFT=tolerated rs5950672 X:544075 G - - - intergenic_variant - - - - - - rs28628376 X:580654 C 6473 NM_006883.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4425 rs28628376 X:580654 C 6473 NM_000451.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4425 rs5946361 X:898313 G - - - intergenic_variant - - - - - - rs5946604 X:932713 C - - - intergenic_variant - - - - - - rs62635781 X:1330888 A 64109 NM_001012288.1 Transcript intron_variant - - - - - - rs62635781 X:1330888 A 64109 NM_022148.2 Transcript intron_variant - - - - - - rs73175728 X:1332413 A 64109 NM_001012288.1 Transcript upstream_gene_variant - - - - - - DISTANCE=886 rs73175728 X:1332413 A 64109 NM_022148.2 Transcript upstream_gene_variant - - - - - - DISTANCE=884 rs310149 X:2595638 A - - - intergenic_variant - - - - - - rs1194777 X:3100573 T - - - intergenic_variant - - - - - - rs813185 X:3310665 C - - - intergenic_variant - - - - - - rs62575734 X:3710609 A - - - intergenic_variant - - - - - - rs6608340 X:3857117 C - - - intergenic_variant - - - - - - rs6529819 X:4088438 C - - - intergenic_variant - - - - - - rs1405306 X:4349555 T - - - intergenic_variant - - - - - - rs2044636 X:4875057 T - - - intergenic_variant - - - - - - rs5916035 X:5191152 T - - - intergenic_variant - - - - - - rs5915535 X:5290770 T - - - intergenic_variant - - - - - - rs5961781 X:5564948 A - ENSR00000474987 RegulatoryFeature regulatory_region_variant - - - - - - rs5961781 X:5564948 A - - - intergenic_variant - - - - - - rs4281234 X:5650771 A - - - intergenic_variant - - - - - - rs5916249 X:5691591 G - - - intergenic_variant - - - - - - rs57654185 X:5785689 G ENSESTG00000009140 ENSESTT00000022944 Transcript intron_variant - - - - - - rs57654185 X:5785689 G ENSESTG00000009140 ENSESTT00000022960 Transcript intron_variant - - - - - - rs57654185 X:5785689 G ENSESTG00000009140 ENSESTT00000022941 Transcript intron_variant - - - - - - rs5978828 X:6965233 C ENSESTG00000004802 ENSESTT00000012213 Transcript downstream_gene_variant - - - - - - DISTANCE=3201 rs5978828 X:6965233 C CCDS48075.1 CCDS48075.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3104 rs5978828 X:6965233 C CCDS48076.1 CCDS48076.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3104 rs5978828 X:6965233 C CCDS55367.1 CCDS55367.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3104 rs5978828 X:6965233 C 8226 NM_001135565.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1728 rs5978828 X:6965233 C 8226 NM_001178136.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1728 rs5978828 X:6965233 C 8226 NM_012080.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1728 rs2950353 X:7091180 T ENSESTG00000004775 ENSESTT00000012101 Transcript intron_variant - - - - - - rs2950353 X:7091180 T ENSESTG00000004775 ENSESTT00000012110 Transcript intron_variant - - - - - - rs4403551 X:7418806 T - ENSR00000475071 RegulatoryFeature regulatory_region_variant - - - - - - rs4403551 X:7418806 T - - - intergenic_variant - - - - - - rs5935392 X:7429927 A - - - intergenic_variant - - - - - - rs5979760 X:7442367 C - - - intergenic_variant - - - - - - rs2017789 X:7594217 G ENSESTG00000004792 ENSESTT00000012149 Transcript intron_variant - - - - - - rs2017789 X:7594217 G ENSESTG00000004792 ENSESTT00000012154 Transcript intron_variant - - - - - - rs1179124 X:7973209 A ENSESTG00000004799 ENSESTT00000012168 Transcript intron_variant - - - - - - rs5933650 X:8331550 A - - - intergenic_variant - - - - - - rs1236391 X:8702043 T CCDS14130.1 CCDS14130.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1966 rs1236391 X:8702043 T ENSESTG00000019323 ENSESTT00000048609 Transcript upstream_gene_variant - - - - - - DISTANCE=1902 rs1236391 X:8702043 T 3730 NM_000216.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1816 rs5933681 X:8754882 G CCDS14131.1 CCDS14131.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4470 rs5933681 X:8754882 G 171482 NM_174951.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3954 rs5933681 X:8754882 G 171482 NM_001171186.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3954 rs4830606 X:8770873 T CCDS14131.1 CCDS14131.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2661 rs4830606 X:8770873 T 171482 NM_174951.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1449 rs4830606 X:8770873 T 171482 NM_001171186.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1495 rs1232136 X:8874681 C - - - intergenic_variant - - - - - - rs5978313 X:9281460 G - ENSR00000475186 RegulatoryFeature regulatory_region_variant - - - - - - rs5978313 X:9281460 G - - - intergenic_variant - - - - - - rs1232175 X:9345194 A - - - intergenic_variant - - - - - - rs2521403 X:9565457 A 6907 NM_005647.3 Transcript intron_variant - - - - - - rs2521403 X:9565457 A ENSESTG00000023778 ENSESTT00000060331 Transcript intron_variant - - - - - - rs2521403 X:9565457 A 6907 NM_001139467.1 Transcript intron_variant - - - - - - rs2521403 X:9565457 A 6907 NM_001139468.1 Transcript intron_variant - - - - - - rs2521403 X:9565457 A ENSESTG00000023778 ENSESTT00000060368 Transcript intron_variant - - - - - - rs2521403 X:9565457 A ENSESTG00000023778 ENSESTT00000060355 Transcript intron_variant - - - - - - rs2521403 X:9565457 A ENSESTG00000023778 ENSESTT00000060212 Transcript intron_variant - - - - - - rs2521403 X:9565457 A 6907 NM_001139466.1 Transcript intron_variant - - - - - - rs2521403 X:9565457 A ENSESTG00000023778 ENSESTT00000060199 Transcript intron_variant - - - - - - rs2521403 X:9565457 A ENSESTG00000023778 ENSESTT00000060299 Transcript intron_variant - - - - - - rs2521388 X:9587617 T 6907 NM_005647.3 Transcript intron_variant - - - - - - rs2521388 X:9587617 T ENSESTG00000023778 ENSESTT00000060331 Transcript intron_variant - - - - - - rs2521388 X:9587617 T 6907 NM_001139467.1 Transcript intron_variant - - - - - - rs2521388 X:9587617 T 6907 NM_001139468.1 Transcript intron_variant - - - - - - rs2521388 X:9587617 T ENSESTG00000023778 ENSESTT00000060368 Transcript intron_variant - - - - - - rs2521388 X:9587617 T ENSESTG00000023778 ENSESTT00000060355 Transcript intron_variant - - - - - - rs2521388 X:9587617 T ENSESTG00000023778 ENSESTT00000060212 Transcript intron_variant - - - - - - rs2521388 X:9587617 T 6907 NM_001139466.1 Transcript intron_variant - - - - - - rs2521388 X:9587617 T ENSESTG00000023778 ENSESTT00000060199 Transcript intron_variant - - - - - - rs2521388 X:9587617 T ENSESTG00000023778 ENSESTT00000060299 Transcript intron_variant - - - - - - rs6419035 X:9791845 C ENSESTG00000023937 ENSESTT00000060500 Transcript intron_variant - - - - - - rs6419035 X:9791845 C 357 NM_001649.2 Transcript intron_variant - - - - - - rs6419035 X:9791845 C CCDS14135.1 CCDS14135.1 Transcript intron_variant - - - - - - rs6419035 X:9791845 C ENSESTG00000023937 ENSESTT00000060445 Transcript intron_variant - - - - - - rs5933776 X:9841311 T ENSESTG00000023937 ENSESTT00000060500 Transcript intron_variant - - - - - - rs5933776 X:9841311 T 357 NM_001649.2 Transcript intron_variant - - - - - - rs5933776 X:9841311 T CCDS14135.1 CCDS14135.1 Transcript intron_variant - - - - - - rs5933776 X:9841311 T ENSESTG00000023937 ENSESTT00000060445 Transcript intron_variant - - - - - - rs5978346 X:9853256 A - ENSR00000475268 RegulatoryFeature regulatory_region_variant - - - - - - rs5978346 X:9853256 A ENSESTG00000023937 ENSESTT00000060500 Transcript intron_variant - - - - - - rs5978346 X:9853256 A 357 NM_001649.2 Transcript intron_variant - - - - - - rs5978346 X:9853256 A CCDS14135.1 CCDS14135.1 Transcript intron_variant - - - - - - rs5978346 X:9853256 A ENSESTG00000023937 ENSESTT00000060445 Transcript intron_variant - - - - - - rs5979200 X:9855904 G ENSESTG00000023937 ENSESTT00000060500 Transcript intron_variant - - - - - - rs5979200 X:9855904 G 357 NM_001649.2 Transcript intron_variant - - - - - - rs5979200 X:9855904 G CCDS14135.1 CCDS14135.1 Transcript intron_variant - - - - - - rs5979200 X:9855904 G ENSESTG00000023937 ENSESTT00000060445 Transcript intron_variant - - - - - - rs4830671 X:9862275 C ENSESTG00000023937 ENSESTT00000060500 Transcript intron_variant - - - - - - rs4830671 X:9862275 C 357 NM_001649.2 Transcript intron_variant - - - - - - rs4830671 X:9862275 C ENSESTG00000024008 ENSESTT00000060609 Transcript upstream_gene_variant - - - - - - DISTANCE=3581 rs4830671 X:9862275 C CCDS14135.1 CCDS14135.1 Transcript intron_variant - - - - - - rs4830671 X:9862275 C ENSESTG00000023937 ENSESTT00000060445 Transcript intron_variant - - - - - - rs5933788 X:9890087 G ENSESTG00000024037 ENSESTT00000060685 Transcript intron_variant - - - - - - rs5933788 X:9890087 G ENSESTG00000024008 ENSESTT00000060659 Transcript intron_variant - - - - - - rs5933788 X:9890087 G ENSESTG00000024008 ENSESTT00000060609 Transcript intron_variant - - - - - - rs5933788 X:9890087 G ENSESTG00000024008 ENSESTT00000060671 Transcript intron_variant - - - - - - rs5933788 X:9890087 G ENSESTG00000023937 ENSESTT00000060500 Transcript intron_variant - - - - - - rs5933788 X:9890087 G 357 NM_001649.2 Transcript intron_variant - - - - - - rs5933788 X:9890087 G CCDS14135.1 CCDS14135.1 Transcript intron_variant - - - - - - rs5933788 X:9890087 G ENSESTG00000023937 ENSESTT00000060445 Transcript intron_variant - - - - - - rs5934717 X:9892443 T ENSESTG00000024037 ENSESTT00000060685 Transcript intron_variant - - - - - - rs5934717 X:9892443 T ENSESTG00000024008 ENSESTT00000060659 Transcript intron_variant - - - - - - rs5934717 X:9892443 T ENSESTG00000024008 ENSESTT00000060609 Transcript intron_variant - - - - - - rs5934717 X:9892443 T ENSESTG00000024008 ENSESTT00000060671 Transcript intron_variant - - - - - - rs5934717 X:9892443 T ENSESTG00000023937 ENSESTT00000060500 Transcript intron_variant - - - - - - rs5934717 X:9892443 T 357 NM_001649.2 Transcript intron_variant - - - - - - rs5934717 X:9892443 T CCDS14135.1 CCDS14135.1 Transcript intron_variant - - - - - - rs5934717 X:9892443 T ENSESTG00000023937 ENSESTT00000060445 Transcript intron_variant - - - - - - rs5934735 X:9946828 A - - - intergenic_variant - - - - - - rs5934739 X:9972180 A - ENSR00000475294 RegulatoryFeature regulatory_region_variant - - - - - - rs5934739 X:9972180 A - - - intergenic_variant - - - - - - rs1468132 X:9994425 G ENSESTG00000009453 ENSESTT00000023787 Transcript intron_variant - - - - - - rs1468132 X:9994425 G ENSESTG00000009453 ENSESTT00000023776 Transcript intron_variant - - - - - - rs1468132 X:9994425 G 55841 NM_015691.3 Transcript intron_variant - - - - - - rs1468132 X:9994425 G ENSESTG00000009453 ENSESTT00000023791 Transcript intron_variant - - - - - - rs728141 X:10020727 G ENSESTG00000009453 ENSESTT00000023787 Transcript intron_variant - - - - - - rs728141 X:10020727 G ENSESTG00000009453 ENSESTT00000023776 Transcript intron_variant - - - - - - rs728141 X:10020727 G 55841 NM_015691.3 Transcript intron_variant - - - - - - rs728141 X:10020727 G ENSESTG00000009453 ENSESTT00000023791 Transcript intron_variant - - - - - - rs768796 X:10037160 G ENSESTG00000009453 ENSESTT00000023787 Transcript intron_variant - - - - - - rs768796 X:10037160 G ENSESTG00000009453 ENSESTT00000023776 Transcript intron_variant - - - - - - rs768796 X:10037160 G CCDS14136.1 CCDS14136.1 Transcript intron_variant - - - - - - rs768796 X:10037160 G 55841 NM_015691.3 Transcript intron_variant - - - - - - rs768796 X:10037160 G ENSESTG00000009453 ENSESTT00000023791 Transcript intron_variant - - - - - - rs1548386 X:10041482 T ENSESTG00000009453 ENSESTT00000023787 Transcript intron_variant - - - - - - rs1548386 X:10041482 T ENSESTG00000009453 ENSESTT00000023776 Transcript intron_variant - - - - - - rs1548386 X:10041482 T CCDS14136.1 CCDS14136.1 Transcript intron_variant - - - - - - rs1548386 X:10041482 T 55841 NM_015691.3 Transcript intron_variant - - - - - - rs1548386 X:10041482 T ENSESTG00000009453 ENSESTT00000023791 Transcript intron_variant - - - - - - rs5934906 X:10409916 C 4281 NM_000381.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3434 rs5934906 X:10409916 C 4281 NM_001098624.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3434 rs5934906 X:10409916 C 4281 NM_033290.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3434 rs5934906 X:10409916 C 4281 NM_001193277.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3434 rs5934906 X:10409916 C 4281 NM_033289.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3434 rs2406511 X:10444699 A ENSESTG00000009571 ENSESTT00000024014 Transcript intron_variant - - - - - - rs2406511 X:10444699 A 4281 NM_001098624.2 Transcript intron_variant - - - - - - rs2406511 X:10444699 A 4281 NM_001193277.1 Transcript intron_variant - - - - - - rs2406511 X:10444699 A 4281 NM_001193279.1 Transcript intron_variant - - - - - - rs2406511 X:10444699 A 4281 NM_001193280.1 Transcript intron_variant - - - - - - rs2406511 X:10444699 A 4281 NM_000381.3 Transcript intron_variant - - - - - - rs2406511 X:10444699 A 4281 NM_033290.3 Transcript intron_variant - - - - - - rs2406511 X:10444699 A CCDS14138.1 CCDS14138.1 Transcript intron_variant - - - - - - rs2406511 X:10444699 A 4281 NM_033289.1 Transcript intron_variant - - - - - - rs2406511 X:10444699 A 4281 NM_001193278.1 Transcript intron_variant - - - - - - rs5934943 X:10961635 C - - - intergenic_variant - - - - - - rs2708505 X:10992742 C ENSESTG00000026350 ENSESTT00000066387 Transcript intron_variant - - - - - - rs2708505 X:10992742 C ENSESTG00000026350 ENSESTT00000066433 Transcript intron_variant - - - - - - rs5933911 X:11662516 G CCDS14140.1 CCDS14140.1 Transcript intron_variant - - - - - - rs5933911 X:11662516 G CCDS14142.1 CCDS14142.1 Transcript intron_variant - - - - - - rs5933911 X:11662516 G 395 NM_013427.2 Transcript intron_variant - - - - - - rs5933911 X:11662516 G 395 NM_006125.2 Transcript intron_variant - - - - - - rs2525879 X:11743597 C - - - intergenic_variant - - - - - - rs2525869 X:11798670 C 10943 NM_078629.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4798 rs2525869 X:11798670 C ENSESTG00000026084 ENSESTT00000065814 Transcript downstream_gene_variant - - - - - - DISTANCE=4868 rs2525869 X:11798670 C 10943 NM_001193270.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4798 rs2525869 X:11798670 C 10943 NM_006800.3 Transcript downstream_gene_variant - - - - - - DISTANCE=4798 rs858092 X:11844264 T - - - intergenic_variant - - - - - - rs1918241 X:11911962 G ENSESTG00000026132 ENSESTT00000065855 Transcript intron_variant - - - - - - rs2023756 X:12237923 T CCDS35201.1 CCDS35201.1 Transcript intron_variant - - - - - - rs2023756 X:12237923 T 9758 NM_014728.3 Transcript intron_variant - - - - - - rs5935309 X:12375565 C CCDS35201.1 CCDS35201.1 Transcript intron_variant - - - - - - rs5935309 X:12375565 C 9758 NM_014728.3 Transcript intron_variant - - - - - - rs2407936 X:12407271 T CCDS35201.1 CCDS35201.1 Transcript intron_variant - - - - - - rs2407936 X:12407271 T 9758 NM_014728.3 Transcript intron_variant - - - - - - rs4618894 X:12622692 T CCDS35201.1 CCDS35201.1 Transcript intron_variant - - - - - - rs4618894 X:12622692 T 9758 NM_014728.3 Transcript intron_variant - - - - - - rs5935375 X:12654859 T CCDS35201.1 CCDS35201.1 Transcript intron_variant - - - - - - rs5935375 X:12654859 T 9758 NM_014728.3 Transcript intron_variant - - - - - - rs2109135 X:12939928 C ENSESTG00000025058 ENSESTT00000063243 Transcript downstream_gene_variant - - - - - - DISTANCE=2288 rs2109135 X:12939928 C 51311 NM_138636.4 Transcript synonymous_variant 2856 2769 923 D gaT/gaC - rs2109135 X:12939928 C CCDS14152.1 CCDS14152.1 Transcript synonymous_variant 2769 2769 923 D gaT/gaC - rs2109135 X:12939928 C ENSESTG00000025075 ENSESTT00000063269 Transcript intron_variant - - - - - - rs5934051 X:13012911 G - - - intergenic_variant - - - - - - rs1230144 X:13108091 C - - - intergenic_variant - - - - - - rs5934078 X:13195951 C - - - intergenic_variant - - - - - - rs6527648 X:13363477 C - ENSR00000475680 RegulatoryFeature regulatory_region_variant - - - - - - rs6527648 X:13363477 C 100133123 NR_045260.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3533 rs5934141 X:14101646 A - - - intergenic_variant - - - - - - rs7876709 X:14311642 G - - - intergenic_variant - - - - - - rs5934173 X:14454831 A - - - intergenic_variant - - - - - - rs5935801 X:14736040 A CCDS48085.1 CCDS48085.1 Transcript intron_variant - - - - - - rs5935801 X:14736040 A 2742 NM_001118885.1 Transcript intron_variant - - - - - - rs5935801 X:14736040 A CCDS14160.1 CCDS14160.1 Transcript intron_variant - - - - - - rs5935801 X:14736040 A ENSESTG00000003632 ENSESTT00000009124 Transcript intron_variant - - - - - - rs5935801 X:14736040 A CCDS55371.1 CCDS55371.1 Transcript intron_variant - - - - - - rs5935801 X:14736040 A ENSESTG00000003632 ENSESTT00000009099 Transcript intron_variant - - - - - - rs5935801 X:14736040 A 2742 NM_002063.3 Transcript intron_variant - - - - - - rs5935801 X:14736040 A ENSESTG00000003632 ENSESTT00000009102 Transcript intron_variant - - - - - - rs5935801 X:14736040 A ENSESTG00000003632 ENSESTT00000009122 Transcript intron_variant - - - - - - rs5935801 X:14736040 A ENSESTG00000003632 ENSESTT00000009127 Transcript intron_variant - - - - - - rs5935801 X:14736040 A 2742 NM_001171942.1 Transcript intron_variant - - - - - - rs5935801 X:14736040 A ENSESTG00000003632 ENSESTT00000009120 Transcript intron_variant - - - - - - rs5935801 X:14736040 A ENSESTG00000003632 ENSESTT00000009145 Transcript intron_variant - - - - - - rs5935801 X:14736040 A 2742 NM_001118886.1 Transcript intron_variant - - - - - - rs5935801 X:14736040 A ENSESTG00000003632 ENSESTT00000009138 Transcript intron_variant - - - - - - rs6418631 X:14927880 C ENSESTG00000003657 ENSESTT00000009189 Transcript intron_variant - - - - - - rs6418631 X:14927880 C 158747 NM_152581.3 Transcript intron_variant - - - - - - rs6418631 X:14927880 C CCDS14162.1 CCDS14162.1 Transcript intron_variant - - - - - - rs6418631 X:14927880 C 158747 NM_001177475.1 Transcript intron_variant - - - - - - rs6418631 X:14927880 C ENSESTG00000020767 ENSESTT00000052056 Transcript upstream_gene_variant - - - - - - DISTANCE=2221 rs6418631 X:14927880 C ENSESTG00000003657 ENSESTT00000009192 Transcript intron_variant - - - - - - rs6418631 X:14927880 C ENSESTG00000003657 ENSESTT00000009197 Transcript intron_variant - - - - - - rs5935894 X:15179359 T - - - intergenic_variant - - - - - - rs1871512 X:15232236 G - ENSR00000475822 RegulatoryFeature regulatory_region_variant - - - - - - rs1871512 X:15232236 G - - - intergenic_variant - - - - - - rs1233072 X:15641772 T ENSESTG00000021209 ENSESTT00000053311 Transcript downstream_gene_variant - - - - - - DISTANCE=4388 rs1233072 X:15641772 T CCDS14170.1 CCDS14170.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4322 rs1233072 X:15641772 T 57393 NM_020665.4 Transcript downstream_gene_variant - - - - - - DISTANCE=3669 rs1233072 X:15641772 T ENSESTG00000020892 ENSESTT00000052381 Transcript downstream_gene_variant - - - - - - DISTANCE=2167 rs4830996 X:15847331 G ENSESTG00000021151 ENSESTT00000053169 Transcript downstream_gene_variant - - - - - - DISTANCE=3912 rs4830996 X:15847331 G ENSESTG00000021151 ENSESTT00000053145 Transcript downstream_gene_variant - - - - - - DISTANCE=3393 rs4830996 X:15847331 G ENSESTG00000021151 ENSESTT00000053138 Transcript downstream_gene_variant - - - - - - DISTANCE=2240 rs4830996 X:15847331 G 8905 NM_003916.3 Transcript intron_variant - - - - - - rs4830996 X:15847331 G ENSESTG00000021151 ENSESTT00000053107 Transcript downstream_gene_variant - - - - - - DISTANCE=1990 rs4830996 X:15847331 G CCDS14173.1 CCDS14173.1 Transcript intron_variant - - - - - - rs4830996 X:15847331 G ENSESTG00000021140 ENSESTT00000053051 Transcript downstream_gene_variant - - - - - - DISTANCE=1926 rs5980235 X:16182018 C 645864 XM_003119193.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3586 rs5980235 X:16182018 C ENSESTG00000005333 ENSESTT00000013553 Transcript upstream_gene_variant - - - - - - DISTANCE=3586 rs2411865 X:16363174 C - - - intergenic_variant - - - - - - rs4463607 X:16522404 C - - - intergenic_variant - - - - - - rs2010456 X:17038993 A 9185 NM_004726.2 Transcript intron_variant - - - - - - rs2010456 X:17038993 A CCDS14180.2 CCDS14180.2 Transcript intron_variant - - - - - - rs2010456 X:17038993 A ENSESTG00000011043 ENSESTT00000027708 Transcript intron_variant - - - - - - rs2010456 X:17038993 A ENSESTG00000011043 ENSESTT00000027725 Transcript intron_variant - - - - - - rs2010456 X:17038993 A ENSESTG00000011043 ENSESTT00000027714 Transcript intron_variant - - - - - - rs2010456 X:17038993 A ENSESTG00000011043 ENSESTT00000027727 Transcript intron_variant - - - - - - rs2010456 X:17038993 A CCDS43919.1 CCDS43919.1 Transcript intron_variant - - - - - - rs2010456 X:17038993 A 9185 NM_001080975.1 Transcript intron_variant - - - - - - rs2114457 X:17062778 A 9185 NM_004726.2 Transcript intron_variant - - - - - - rs2114457 X:17062778 A CCDS14180.2 CCDS14180.2 Transcript intron_variant - - - - - - rs2114457 X:17062778 A ENSESTG00000011043 ENSESTT00000027708 Transcript intron_variant - - - - - - rs2114457 X:17062778 A ENSESTG00000011043 ENSESTT00000027725 Transcript intron_variant - - - - - - rs2114457 X:17062778 A ENSESTG00000011043 ENSESTT00000027727 Transcript intron_variant - - - - - - rs2114457 X:17062778 A ENSESTG00000011043 ENSESTT00000027728 Transcript intron_variant - - - - - - rs2114457 X:17062778 A CCDS43919.1 CCDS43919.1 Transcript intron_variant - - - - - - rs2114457 X:17062778 A 9185 NM_001080975.1 Transcript intron_variant - - - - - - rs4278262 X:17551596 G 4810 NM_198270.2 Transcript intron_variant - - - - - - rs4278262 X:17551596 G CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs4278262 X:17551596 G ENSESTG00000011078 ENSESTT00000027788 Transcript intron_variant - - - - - - rs6632992 X:17575566 T 4810 NM_198270.2 Transcript intron_variant - - - - - - rs6632992 X:17575566 T CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs6632992 X:17575566 T ENSESTG00000011078 ENSESTT00000027788 Transcript intron_variant - - - - - - rs2384828 X:17594243 C 4810 NM_198270.2 Transcript intron_variant - - - - - - rs2384828 X:17594243 C CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs2384828 X:17594243 C ENSESTG00000011078 ENSESTT00000027788 Transcript intron_variant - - - - - - rs5909453 X:17610416 G - ENSR00001488690 RegulatoryFeature regulatory_region_variant - - - - - - rs5909453 X:17610416 G 4810 NM_198270.2 Transcript intron_variant - - - - - - rs5909453 X:17610416 G CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs4825365 X:17627077 G - ENSR00000476071 RegulatoryFeature regulatory_region_variant - - - - - - rs4825365 X:17627077 G 4810 NM_198270.2 Transcript intron_variant - - - - - - rs4825365 X:17627077 G CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs982212 X:17666436 C 4810 NM_198270.2 Transcript intron_variant - - - - - - rs982212 X:17666436 C ENSESTG00000011100 ENSESTT00000027853 Transcript intron_variant - - - - - - rs982212 X:17666436 C CCDS48087.1 CCDS48087.1 Transcript intron_variant - - - - - - rs982212 X:17666436 C CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs982212 X:17666436 C 4810 NM_001136024.2 Transcript intron_variant - - - - - - rs1894584 X:17668369 A 4810 NM_198270.2 Transcript intron_variant - - - - - - rs1894584 X:17668369 A ENSESTG00000011100 ENSESTT00000027853 Transcript intron_variant - - - - - - rs1894584 X:17668369 A CCDS48087.1 CCDS48087.1 Transcript intron_variant - - - - - - rs1894584 X:17668369 A CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs1894584 X:17668369 A 4810 NM_001136024.2 Transcript intron_variant - - - - - - rs5955513 X:17675264 A 4810 NM_198270.2 Transcript intron_variant - - - - - - rs5955513 X:17675264 A ENSESTG00000011100 ENSESTT00000027853 Transcript intron_variant - - - - - - rs5955513 X:17675264 A CCDS48087.1 CCDS48087.1 Transcript intron_variant - - - - - - rs5955513 X:17675264 A CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs5955513 X:17675264 A 4810 NM_001136024.2 Transcript intron_variant - - - - - - rs978159 X:17677599 T 4810 NM_198270.2 Transcript intron_variant - - - - - - rs978159 X:17677599 T ENSESTG00000011100 ENSESTT00000027853 Transcript intron_variant - - - - - - rs978159 X:17677599 T CCDS48087.1 CCDS48087.1 Transcript intron_variant - - - - - - rs978159 X:17677599 T CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs978159 X:17677599 T 4810 NM_001136024.2 Transcript intron_variant - - - - - - rs978869 X:17691042 A 4810 NM_198270.2 Transcript intron_variant - - - - - - rs978869 X:17691042 A ENSESTG00000011100 ENSESTT00000027853 Transcript intron_variant - - - - - - rs978869 X:17691042 A CCDS48087.1 CCDS48087.1 Transcript intron_variant - - - - - - rs978869 X:17691042 A CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs978869 X:17691042 A 4810 NM_001136024.2 Transcript intron_variant - - - - - - rs5909113 X:17709902 A 4810 NM_198270.2 Transcript intron_variant - - - - - - rs5909113 X:17709902 A ENSESTG00000011100 ENSESTT00000027853 Transcript intron_variant - - - - - - rs5909113 X:17709902 A CCDS48087.1 CCDS48087.1 Transcript intron_variant - - - - - - rs5909113 X:17709902 A CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs5909113 X:17709902 A 4810 NM_001136024.2 Transcript intron_variant - - - - - - rs5955561 X:17726151 A 4810 NM_198270.2 Transcript intron_variant - - - - - - rs5955561 X:17726151 A ENSESTG00000011100 ENSESTT00000027853 Transcript intron_variant - - - - - - rs5955561 X:17726151 A CCDS48087.1 CCDS48087.1 Transcript intron_variant - - - - - - rs5955561 X:17726151 A CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs5955561 X:17726151 A 4810 NM_001136024.2 Transcript intron_variant - - - - - - rs2040423 X:17727009 T 4810 NM_198270.2 Transcript intron_variant - - - - - - rs2040423 X:17727009 T ENSESTG00000011100 ENSESTT00000027853 Transcript intron_variant - - - - - - rs2040423 X:17727009 T CCDS48087.1 CCDS48087.1 Transcript intron_variant - - - - - - rs2040423 X:17727009 T CCDS14181.1 CCDS14181.1 Transcript intron_variant - - - - - - rs2040423 X:17727009 T 4810 NM_001136024.2 Transcript intron_variant - - - - - - rs5909331 X:17753436 T 4810 NM_198270.2 Transcript 3_prime_UTR_variant 8083 - - - - - rs5909331 X:17753436 T 6322 NM_001037536.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2156 rs5909331 X:17753436 T CCDS14181.1 CCDS14181.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2852 rs5909331 X:17753436 T ENSESTG00000011089 ENSESTT00000027819 Transcript upstream_gene_variant - - - - - - DISTANCE=2235 rs5909331 X:17753436 T 6322 NM_001037540.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2156 rs5909331 X:17753436 T 4810 NM_001136024.2 Transcript 3_prime_UTR_variant 7551 - - - - - rs5909331 X:17753436 T ENSESTG00000011089 ENSESTT00000027820 Transcript upstream_gene_variant - - - - - - DISTANCE=2280 rs5909331 X:17753436 T CCDS48087.1 CCDS48087.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2852 rs5909331 X:17753436 T ENSESTG00000011100 ENSESTT00000027853 Transcript intron_variant - - - - - - rs5909331 X:17753436 T 6322 NM_001037535.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2156 rs5909331 X:17753436 T 6322 NM_006746.4 Transcript upstream_gene_variant - - - - - - DISTANCE=2156 rs981443 X:17815414 T - ENSR00000476096 RegulatoryFeature regulatory_region_variant - - - - - - rs981443 X:17815414 T 10742 NM_001172743.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2755 rs981443 X:17815414 T 10742 NR_033349.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2755 rs981443 X:17815414 T 10742 NR_033348.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2755 rs981443 X:17815414 T 10742 NM_001172732.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2755 rs981443 X:17815414 T 10742 NM_001172739.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2755 rs981443 X:17815414 T CCDS55374.1 CCDS55374.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3124 rs981443 X:17815414 T CCDS14183.1 CCDS14183.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3124 rs981443 X:17815414 T ENSESTG00000011095 ENSESTT00000027841 Transcript downstream_gene_variant - - - - - - DISTANCE=4385 rs981443 X:17815414 T 10742 NM_021785.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2755 rs1547423 X:17816632 G 10742 NM_001172743.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1537 rs1547423 X:17816632 G 10742 NR_033349.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1537 rs1547423 X:17816632 G 10742 NR_033348.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1537 rs1547423 X:17816632 G 10742 NM_001172732.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1537 rs1547423 X:17816632 G 10742 NM_001172739.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1537 rs1547423 X:17816632 G CCDS55374.1 CCDS55374.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1906 rs1547423 X:17816632 G CCDS14183.1 CCDS14183.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1906 rs1547423 X:17816632 G ENSESTG00000011095 ENSESTT00000027841 Transcript downstream_gene_variant - - - - - - DISTANCE=3167 rs1547423 X:17816632 G 10742 NM_021785.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1537 rs4239994 X:17840190 C 10742 NM_001172743.1 Transcript intron_variant - - - - - - rs4239994 X:17840190 C 10742 NR_033349.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4239994 X:17840190 C 10742 NM_001172739.1 Transcript intron_variant - - - - - - rs4239994 X:17840190 C 10742 NR_033348.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4239994 X:17840190 C 10742 NM_001172732.1 Transcript intron_variant - - - - - - rs4239994 X:17840190 C ENSESTG00000011095 ENSESTT00000027841 Transcript intron_variant - - - - - - rs4239994 X:17840190 C 10742 NM_021785.4 Transcript intron_variant - - - - - - rs4239995 X:17840283 A 10742 NM_001172743.1 Transcript intron_variant - - - - - - rs4239995 X:17840283 A 10742 NR_033349.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4239995 X:17840283 A 10742 NM_001172739.1 Transcript intron_variant - - - - - - rs4239995 X:17840283 A 10742 NR_033348.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4239995 X:17840283 A 10742 NM_001172732.1 Transcript intron_variant - - - - - - rs4239995 X:17840283 A ENSESTG00000011095 ENSESTT00000027841 Transcript intron_variant - - - - - - rs4239995 X:17840283 A 10742 NM_021785.4 Transcript intron_variant - - - - - - rs1894582 X:17846933 C 10742 NM_001172743.1 Transcript intron_variant - - - - - - rs1894582 X:17846933 C 10742 NR_033349.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1894582 X:17846933 C 10742 NM_001172739.1 Transcript intron_variant - - - - - - rs1894582 X:17846933 C 10742 NR_033348.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1894582 X:17846933 C 10742 NM_001172732.1 Transcript intron_variant - - - - - - rs1894582 X:17846933 C ENSESTG00000011095 ENSESTT00000027841 Transcript intron_variant - - - - - - rs1894582 X:17846933 C 10742 NM_021785.4 Transcript intron_variant - - - - - - rs12833886 X:17854167 G 10742 NM_001172743.1 Transcript intron_variant - - - - - - rs12833886 X:17854167 G 10742 NR_033349.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs12833886 X:17854167 G 10742 NM_001172739.1 Transcript intron_variant - - - - - - rs12833886 X:17854167 G 10742 NR_033348.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs12833886 X:17854167 G 10742 NM_001172732.1 Transcript intron_variant - - - - - - rs12833886 X:17854167 G ENSESTG00000011095 ENSESTT00000027841 Transcript intron_variant - - - - - - rs12833886 X:17854167 G 10742 NM_021785.4 Transcript intron_variant - - - - - - rs5909388 X:18139993 G - - - intergenic_variant - - - - - - rs5909145 X:18145379 C - - - intergenic_variant - - - - - - rs5909146 X:18145707 C - - - intergenic_variant - - - - - - rs6527846 X:18347984 G 10389 NM_006089.2 Transcript intron_variant - - - - - - rs6527846 X:18347984 G ENSESTG00000004320 ENSESTT00000010896 Transcript intron_variant - - - - - - rs6527846 X:18347984 G 10389 NR_033717.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6527846 X:18347984 G ENSESTG00000004320 ENSESTT00000010909 Transcript intron_variant - - - - - - rs6527846 X:18347984 G CCDS14185.1 CCDS14185.1 Transcript intron_variant - - - - - - rs4825233 X:18686308 G CCDS14187.1 CCDS14187.1 Transcript intron_variant - - - - - - rs4825233 X:18686308 G 6247 NM_000330.3 Transcript intron_variant - - - - - - rs5909192 X:18698041 C 100189191 NC_000023.10:TRNAV19:u_t_1 Transcript upstream_gene_variant - - - - - - DISTANCE=4940 rs5909193 X:18698109 A - - - intergenic_variant - - - - - - rs5909224 X:18769306 T CCDS43920.1 CCDS43920.1 Transcript intron_variant - - - - - - rs5909224 X:18769306 T CCDS14188.1 CCDS14188.1 Transcript intron_variant - - - - - - rs5909224 X:18769306 T 5475 NM_152226.1 Transcript intron_variant - - - - - - rs5909224 X:18769306 T ENSESTG00000004294 ENSESTT00000010831 Transcript intron_variant - - - - - - rs5909224 X:18769306 T 5475 NM_006240.2 Transcript intron_variant - - - - - - rs5909224 X:18769306 T 5475 NM_152224.1 Transcript intron_variant - - - - - - rs5909228 X:18771721 G CCDS43920.1 CCDS43920.1 Transcript intron_variant - - - - - - rs5909228 X:18771721 G CCDS14188.1 CCDS14188.1 Transcript intron_variant - - - - - - rs5909228 X:18771721 G 5475 NM_152226.1 Transcript intron_variant - - - - - - rs5909228 X:18771721 G ENSESTG00000004294 ENSESTT00000010831 Transcript intron_variant - - - - - - rs5909228 X:18771721 G 5475 NM_006240.2 Transcript intron_variant - - - - - - rs5909228 X:18771721 G 5475 NM_152224.1 Transcript intron_variant - - - - - - rs5909230 X:18772453 G CCDS43920.1 CCDS43920.1 Transcript intron_variant - - - - - - rs5909230 X:18772453 G CCDS14188.1 CCDS14188.1 Transcript intron_variant - - - - - - rs5909230 X:18772453 G 5475 NM_152226.1 Transcript intron_variant - - - - - - rs5909230 X:18772453 G ENSESTG00000004294 ENSESTT00000010831 Transcript intron_variant - - - - - - rs5909230 X:18772453 G 5475 NM_006240.2 Transcript intron_variant - - - - - - rs5909230 X:18772453 G 5475 NM_152224.1 Transcript intron_variant - - - - - - rs5909234 X:18784279 G CCDS43920.1 CCDS43920.1 Transcript intron_variant - - - - - - rs5909234 X:18784279 G CCDS14188.1 CCDS14188.1 Transcript intron_variant - - - - - - rs5909234 X:18784279 G 5475 NM_152226.1 Transcript intron_variant - - - - - - rs5909234 X:18784279 G ENSESTG00000004294 ENSESTT00000010831 Transcript intron_variant - - - - - - rs5909234 X:18784279 G 5475 NM_006240.2 Transcript intron_variant - - - - - - rs5909234 X:18784279 G 5475 NM_152224.1 Transcript intron_variant - - - - - - rs5909236 X:18792760 T CCDS43920.1 CCDS43920.1 Transcript intron_variant - - - - - - rs5909236 X:18792760 T CCDS14188.1 CCDS14188.1 Transcript intron_variant - - - - - - rs5909236 X:18792760 T 5475 NM_152226.1 Transcript intron_variant - - - - - - rs5909236 X:18792760 T ENSESTG00000004294 ENSESTT00000010831 Transcript intron_variant - - - - - - rs5909236 X:18792760 T 5475 NM_006240.2 Transcript intron_variant - - - - - - rs5909236 X:18792760 T 5475 NM_152224.1 Transcript intron_variant - - - - - - rs6527870 X:18799844 T CCDS43920.1 CCDS43920.1 Transcript intron_variant - - - - - - rs6527870 X:18799844 T CCDS14188.1 CCDS14188.1 Transcript intron_variant - - - - - - rs6527870 X:18799844 T 5475 NM_152226.1 Transcript intron_variant - - - - - - rs6527870 X:18799844 T ENSESTG00000004294 ENSESTT00000010831 Transcript intron_variant - - - - - - rs6527870 X:18799844 T 5475 NM_006240.2 Transcript intron_variant - - - - - - rs6527870 X:18799844 T 5475 NM_152224.1 Transcript intron_variant - - - - - - rs6527872 X:18811346 C - ENSR00000476152 RegulatoryFeature regulatory_region_variant - - - - - - rs6527872 X:18811346 C CCDS43920.1 CCDS43920.1 Transcript intron_variant - - - - - - rs6527872 X:18811346 C CCDS14188.1 CCDS14188.1 Transcript intron_variant - - - - - - rs6527872 X:18811346 C 5475 NM_152226.1 Transcript intron_variant - - - - - - rs6527872 X:18811346 C ENSESTG00000004294 ENSESTT00000010831 Transcript downstream_gene_variant - - - - - - DISTANCE=4030 rs6527872 X:18811346 C 5475 NM_006240.2 Transcript intron_variant - - - - - - rs6527872 X:18811346 C 5475 NM_152224.1 Transcript intron_variant - - - - - - rs6633141 X:18815295 A CCDS43920.1 CCDS43920.1 Transcript intron_variant - - - - - - rs6633141 X:18815295 A CCDS14188.1 CCDS14188.1 Transcript intron_variant - - - - - - rs6633141 X:18815295 A 5475 NM_152226.1 Transcript intron_variant - - - - - - rs6633141 X:18815295 A 5475 NM_006240.2 Transcript intron_variant - - - - - - rs6633141 X:18815295 A 5475 NM_152224.1 Transcript intron_variant - - - - - - rs4825247 X:19834983 T CCDS14193.1 CCDS14193.1 Transcript intron_variant - - - - - - rs4825247 X:19834983 T ENSESTG00000009178 ENSESTT00000023108 Transcript intron_variant - - - - - - rs4825247 X:19834983 T 30011 NM_031892.2 Transcript intron_variant - - - - - - rs5909137 X:20297477 G - - - intergenic_variant - - - - - - rs5990833 X:20702055 C - - - intergenic_variant - - - - - - rs9306762 X:21204522 T - - - intergenic_variant - - - - - - rs6633409 X:21396762 A CCDS55388.1 CCDS55388.1 Transcript intron_variant - - - - - - rs6633409 X:21396762 A 22866 NM_001168649.1 Transcript intron_variant - - - - - - rs6633409 X:21396762 A CCDS14198.1 CCDS14198.1 Transcript intron_variant - - - - - - rs6633409 X:21396762 A CCDS55387.1 CCDS55387.1 Transcript intron_variant - - - - - - rs6633409 X:21396762 A CCDS55389.1 CCDS55389.1 Transcript intron_variant - - - - - - rs6633409 X:21396762 A 22866 NM_014927.3 Transcript intron_variant - - - - - - rs6633409 X:21396762 A 22866 NM_001168647.1 Transcript intron_variant - - - - - - rs6633409 X:21396762 A ENSESTG00000012222 ENSESTT00000030589 Transcript upstream_gene_variant - - - - - - DISTANCE=4525 rs6633409 X:21396762 A 22866 NM_001168648.1 Transcript intron_variant - - - - - - rs6633409 X:21396762 A ENSESTG00000012119 ENSESTT00000030325 Transcript intron_variant - - - - - - rs1348900 X:21512397 A CCDS55388.1 CCDS55388.1 Transcript intron_variant - - - - - - rs1348900 X:21512397 A 22866 NM_001168649.1 Transcript intron_variant - - - - - - rs1348900 X:21512397 A CCDS14198.1 CCDS14198.1 Transcript intron_variant - - - - - - rs1348900 X:21512397 A CCDS55387.1 CCDS55387.1 Transcript intron_variant - - - - - - rs1348900 X:21512397 A CCDS55389.1 CCDS55389.1 Transcript intron_variant - - - - - - rs1348900 X:21512397 A 22866 NM_014927.3 Transcript intron_variant - - - - - - rs1348900 X:21512397 A 22866 NM_001168647.1 Transcript intron_variant - - - - - - rs1348900 X:21512397 A 22866 NM_001168648.1 Transcript intron_variant - - - - - - rs1348900 X:21512397 A ENSESTG00000012126 ENSESTT00000030346 Transcript intron_variant - - - - - - rs5904591 X:21879891 A ENSESTG00000012148 ENSESTT00000030446 Transcript intron_variant - - - - - - rs5904591 X:21879891 A CCDS14201.1 CCDS14201.1 Transcript intron_variant - - - - - - rs5904591 X:21879891 A ENSESTG00000012148 ENSESTT00000030463 Transcript intron_variant - - - - - - rs5904591 X:21879891 A ENSESTG00000012148 ENSESTT00000030426 Transcript intron_variant - - - - - - rs5904591 X:21879891 A 51360 NM_015884.3 Transcript intron_variant - - - - - - rs5904591 X:21879891 A CCDS14202.1 CCDS14202.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4170 rs5904591 X:21879891 A 404281 NM_206923.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3046 rs5904493 X:21897209 C ENSESTG00000012148 ENSESTT00000030446 Transcript intron_variant - - - - - - rs5904493 X:21897209 C CCDS14201.1 CCDS14201.1 Transcript intron_variant - - - - - - rs5904493 X:21897209 C ENSESTG00000012148 ENSESTT00000030463 Transcript intron_variant - - - - - - rs5904493 X:21897209 C ENSESTG00000012148 ENSESTT00000030426 Transcript intron_variant - - - - - - rs5904493 X:21897209 C ENSESTG00000001289 ENSESTT00000003044 Transcript upstream_gene_variant - - - - - - DISTANCE=1819 rs5904493 X:21897209 C 51360 NM_015884.3 Transcript intron_variant - - - - - - rs4824177 X:22131950 G ENSESTG00000001387 ENSESTT00000003266 Transcript downstream_gene_variant - - - - - - DISTANCE=2271 rs4824177 X:22131950 G CCDS14204.1 CCDS14204.1 Transcript intron_variant - - - - - - rs4824177 X:22131950 G ENSESTG00000001387 ENSESTT00000003263 Transcript intron_variant - - - - - - rs4824177 X:22131950 G 5251 NM_000444.4 Transcript intron_variant - - - - - - rs5951715 X:22196078 T CCDS14204.1 CCDS14204.1 Transcript intron_variant - - - - - - rs5951715 X:22196078 T 5251 NM_000444.4 Transcript intron_variant - - - - - - rs5951715 X:22196078 T ENSESTG00000001399 ENSESTT00000003293 Transcript intron_variant - - - - - - rs5951715 X:22196078 T 100873942 NR_046639.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4978 rs1894420 X:22273044 G ENSESTG00000001433 ENSESTT00000003380 Transcript intron_variant - - - - - - rs1894420 X:22273044 G 100873065 NR_073010.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4870 rs1894421 X:22273051 G ENSESTG00000001433 ENSESTT00000003380 Transcript intron_variant - - - - - - rs1894421 X:22273051 G 100873065 NR_073010.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4863 rs6528118 X:22383457 T - ENSR00001488896 RegulatoryFeature regulatory_region_variant - - - - - - rs6528118 X:22383457 T 100873065 NR_073010.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1507800 X:22575806 A 100873065 NR_073010.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs6528179 X:22771406 T 100873065 NR_073010.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4828950 X:23003965 G 100873065 NR_073010.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5925735 X:23182884 C 100873065 NR_073010.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2189673 X:23273765 G 100873065 NR_073010.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5925847 X:23608593 T - - - intergenic_variant - - - - - - rs2704846 X:24177104 T 7543 NM_001178086.1 Transcript intron_variant - - - - - - rs2704846 X:24177104 T ENSESTG00000023122 ENSESTT00000058437 Transcript intron_variant - - - - - - rs2704846 X:24177104 T 7543 NM_003410.3 Transcript intron_variant - - - - - - rs2704846 X:24177104 T ENSESTG00000023122 ENSESTT00000058488 Transcript intron_variant - - - - - - rs2704846 X:24177104 T ENSESTG00000023122 ENSESTT00000058465 Transcript intron_variant - - - - - - rs2704846 X:24177104 T 7543 NM_001178095.1 Transcript intron_variant - - - - - - rs2704846 X:24177104 T 7543 NM_001178085.1 Transcript intron_variant - - - - - - rs2704846 X:24177104 T 7543 NM_001178084.1 Transcript intron_variant - - - - - - rs2704846 X:24177104 T ENSESTG00000023122 ENSESTT00000058459 Transcript intron_variant - - - - - - rs2704846 X:24177104 T ENSESTG00000023122 ENSESTT00000058495 Transcript intron_variant - - - - - - rs2704846 X:24177104 T ENSESTG00000023122 ENSESTT00000058510 Transcript intron_variant - - - - - - rs5949269 X:24358982 T - - - intergenic_variant - - - - - - rs2107420 X:24442844 A - - - intergenic_variant - - - - - - rs2905999 X:24729472 C CCDS14214.1 CCDS14214.1 Transcript intron_variant - - - - - - rs2905999 X:24729472 C 5422 NM_016937.3 Transcript intron_variant - - - - - - rs2905999 X:24729472 C ENSESTG00000023451 ENSESTT00000059126 Transcript intron_variant - - - - - - rs75310488 X:24751958 C CCDS14214.1 CCDS14214.1 Transcript intron_variant - - - - - - rs75310488 X:24751958 C 5422 NM_016937.3 Transcript intron_variant - - - - - - rs5944711 X:25047080 T - ENSR00000476666 RegulatoryFeature regulatory_region_variant - - - - - - rs5944711 X:25047080 T ENSESTG00000035531 ENSESTT00000089742 Transcript downstream_gene_variant - - - - - - DISTANCE=1037 rs5944144 X:25767174 C ENSESTG00000035527 ENSESTT00000089736 Transcript intron_variant - - - - - - rs2340470 X:25830693 T ENSESTG00000035527 ENSESTT00000089736 Transcript intron_variant - - - - - - rs6630167 X:25886433 G ENSESTG00000035527 ENSESTT00000089736 Transcript intron_variant - - - - - - rs6418575 X:26403954 G - - - intergenic_variant - - - - - - rs2315936 X:26405277 G - - - intergenic_variant - - - - - - rs5944484 X:26518322 G - - - intergenic_variant - - - - - - rs5986625 X:26598902 C - - - intergenic_variant - - - - - - rs5971271 X:27032523 G - - - intergenic_variant - - - - - - rs1898743 X:27074056 T - - - intergenic_variant - - - - - - rs2109569 X:27483753 C 139420 NR_002784.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2295 rs436991 X:27591616 A - - - intergenic_variant - - - - - - rs196981 X:28709128 C 11141 NM_014271.3 Transcript intron_variant - - - - - - rs5943616 X:29227842 G 11141 NM_014271.3 Transcript intron_variant - - - - - - rs5943616 X:29227842 G CCDS14218.1 CCDS14218.1 Transcript intron_variant - - - - - - rs6653819 X:29544512 T 11141 NM_014271.3 Transcript intron_variant - - - - - - rs6653819 X:29544512 T CCDS14218.1 CCDS14218.1 Transcript intron_variant - - - - - - rs5927629 X:30872602 G CCDS14226.1 CCDS14226.1 Transcript missense_variant 1180 1180 394 W/R Tgg/Cgg - PolyPhen=benign;SIFT=tolerated rs5927629 X:30872602 G 257397 NM_152787.3 Transcript missense_variant 1843 1180 394 W/R Tgg/Cgg - PolyPhen=benign;SIFT=tolerated rs6527064 X:31168622 G CCDS14231.1 CCDS14231.1 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004006.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_000109.3 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004023.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004015.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004021.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004014.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G ENSESTG00000016659 ENSESTT00000041843 Transcript intron_variant - - - - - - rs6527064 X:31168622 G CCDS14234.1 CCDS14234.1 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004007.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G CCDS55395.1 CCDS55395.1 Transcript intron_variant - - - - - - rs6527064 X:31168622 G CCDS14232.1 CCDS14232.1 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004010.3 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004022.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G CCDS48091.1 CCDS48091.1 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004009.3 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004016.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004018.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G CCDS14233.1 CCDS14233.1 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004013.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004020.3 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004017.2 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004011.3 Transcript intron_variant - - - - - - rs6527064 X:31168622 G ENSESTG00000016659 ENSESTT00000041833 Transcript intron_variant - - - - - - rs6527064 X:31168622 G CCDS55394.1 CCDS55394.1 Transcript intron_variant - - - - - - rs6527064 X:31168622 G ENSESTG00000016659 ENSESTT00000041816 Transcript intron_variant - - - - - - rs6527064 X:31168622 G 1756 NM_004012.3 Transcript intron_variant - - - - - - rs331336 X:32347172 T 1756 NM_004010.3 Transcript intron_variant - - - - - - rs331336 X:32347172 T 1756 NM_004006.2 Transcript intron_variant - - - - - - rs331336 X:32347172 T 1756 NM_000109.3 Transcript intron_variant - - - - - - rs331336 X:32347172 T 1756 NM_004009.3 Transcript intron_variant - - - - - - rs331336 X:32347172 T CCDS14233.1 CCDS14233.1 Transcript intron_variant - - - - - - rs331336 X:32347172 T 1756 NM_004007.2 Transcript intron_variant - - - - - - rs331336 X:32347172 T CCDS55395.1 CCDS55395.1 Transcript intron_variant - - - - - - rs331336 X:32347172 T 1756 NM_004011.3 Transcript intron_variant - - - - - - rs331336 X:32347172 T 1756 NM_004012.3 Transcript intron_variant - - - - - - rs5928093 X:32872170 T 1756 NM_004010.3 Transcript intron_variant - - - - - - rs5928093 X:32872170 T 1756 NM_004006.2 Transcript intron_variant - - - - - - rs5928093 X:32872170 T 1756 NM_000109.3 Transcript intron_variant - - - - - - rs5928093 X:32872170 T ENSESTG00000033667 ENSESTT00000085098 Transcript intron_variant - - - - - - rs5928093 X:32872170 T 1756 NM_004009.3 Transcript intron_variant - - - - - - rs5928093 X:32872170 T CCDS14233.1 CCDS14233.1 Transcript intron_variant - - - - - - rs5928093 X:32872170 T 1756 NM_004007.2 Transcript intron_variant - - - - - - rs5928093 X:32872170 T CCDS55395.1 CCDS55395.1 Transcript intron_variant - - - - - - rs5928093 X:32872170 T ENSESTG00000033667 ENSESTT00000085109 Transcript intron_variant - - - - - - rs5928093 X:32872170 T ENSESTG00000033667 ENSESTT00000085104 Transcript intron_variant - - - - - - rs2406354 X:32958995 G 1756 NM_004010.3 Transcript intron_variant - - - - - - rs2406354 X:32958995 G 1756 NM_004006.2 Transcript intron_variant - - - - - - rs2406354 X:32958995 G 1756 NM_000109.3 Transcript intron_variant - - - - - - rs2406354 X:32958995 G ENSESTG00000033667 ENSESTT00000085098 Transcript intron_variant - - - - - - rs2406354 X:32958995 G 1756 NM_004009.3 Transcript intron_variant - - - - - - rs2406354 X:32958995 G CCDS14233.1 CCDS14233.1 Transcript intron_variant - - - - - - rs2406354 X:32958995 G 1756 NM_004007.2 Transcript intron_variant - - - - - - rs2406354 X:32958995 G CCDS55395.1 CCDS55395.1 Transcript intron_variant - - - - - - rs2406354 X:32958995 G ENSESTG00000033667 ENSESTT00000085109 Transcript intron_variant - - - - - - rs2406354 X:32958995 G ENSESTG00000033667 ENSESTT00000085104 Transcript intron_variant - - - - - - rs5928123 X:32977414 C 1756 NM_004010.3 Transcript intron_variant - - - - - - rs5928123 X:32977414 C 1756 NM_004006.2 Transcript intron_variant - - - - - - rs5928123 X:32977414 C 1756 NM_000109.3 Transcript intron_variant - - - - - - rs5928123 X:32977414 C ENSESTG00000033667 ENSESTT00000085098 Transcript intron_variant - - - - - - rs5928123 X:32977414 C 1756 NM_004009.3 Transcript intron_variant - - - - - - rs5928123 X:32977414 C CCDS14233.1 CCDS14233.1 Transcript intron_variant - - - - - - rs5928123 X:32977414 C 1756 NM_004007.2 Transcript intron_variant - - - - - - rs5928123 X:32977414 C CCDS55395.1 CCDS55395.1 Transcript intron_variant - - - - - - rs5928123 X:32977414 C ENSESTG00000033667 ENSESTT00000085109 Transcript intron_variant - - - - - - rs5928123 X:32977414 C ENSESTG00000033667 ENSESTT00000085104 Transcript intron_variant - - - - - - rs5972725 X:33005233 G - ENSR00000477053 RegulatoryFeature regulatory_region_variant - - - - - - rs5972725 X:33005233 G 1756 NM_004010.3 Transcript intron_variant - - - - - - rs5972725 X:33005233 G 1756 NM_004006.2 Transcript intron_variant - - - - - - rs5972725 X:33005233 G 1756 NM_000109.3 Transcript intron_variant - - - - - - rs5972725 X:33005233 G ENSESTG00000033667 ENSESTT00000085098 Transcript intron_variant - - - - - - rs5972725 X:33005233 G 1756 NM_004009.3 Transcript intron_variant - - - - - - rs5972725 X:33005233 G CCDS14233.1 CCDS14233.1 Transcript intron_variant - - - - - - rs5972725 X:33005233 G 1756 NM_004007.2 Transcript intron_variant - - - - - - rs5972725 X:33005233 G CCDS55395.1 CCDS55395.1 Transcript intron_variant - - - - - - rs5972725 X:33005233 G ENSESTG00000033667 ENSESTT00000085109 Transcript intron_variant - - - - - - rs5972725 X:33005233 G ENSESTG00000033667 ENSESTT00000085104 Transcript intron_variant - - - - - - rs2765378 X:33034586 C 1756 NM_004010.3 Transcript intron_variant - - - - - - rs2765378 X:33034586 C 1756 NM_004006.2 Transcript intron_variant - - - - - - rs2765378 X:33034586 C 1756 NM_000109.3 Transcript intron_variant - - - - - - rs2765378 X:33034586 C ENSESTG00000033667 ENSESTT00000085098 Transcript intron_variant - - - - - - rs2765378 X:33034586 C 1756 NM_004009.3 Transcript intron_variant - - - - - - rs2765378 X:33034586 C CCDS14233.1 CCDS14233.1 Transcript intron_variant - - - - - - rs2765378 X:33034586 C ENSESTG00000002679 ENSESTT00000006661 Transcript downstream_gene_variant - - - - - - DISTANCE=3669 rs2765378 X:33034586 C 1756 NM_004007.2 Transcript intron_variant - - - - - - rs2765378 X:33034586 C ENSESTG00000002679 ENSESTT00000006668 Transcript downstream_gene_variant - - - - - - DISTANCE=3668 rs2765378 X:33034586 C CCDS55395.1 CCDS55395.1 Transcript intron_variant - - - - - - rs2765378 X:33034586 C ENSESTG00000033667 ENSESTT00000085109 Transcript intron_variant - - - - - - rs2765378 X:33034586 C ENSESTG00000033667 ENSESTT00000085104 Transcript intron_variant - - - - - - rs5972886 X:33590957 G - - - intergenic_variant - - - - - - rs1518973 X:33630399 G - - - intergenic_variant - - - - - - rs1870678 X:33787398 T - - - intergenic_variant - - - - - - rs2446937 X:33834158 A - - - intergenic_variant - - - - - - rs4829142 X:34118199 A - - - intergenic_variant - - - - - - rs5928562 X:34472545 C - - - intergenic_variant - - - - - - rs5928573 X:34491170 C - - - intergenic_variant - - - - - - rs4465117 X:34569397 G - - - intergenic_variant - - - - - - rs5973215 X:34626769 A - - - intergenic_variant - - - - - - rs4557862 X:35138752 A - - - intergenic_variant - - - - - - rs1539048 X:35696888 G - - - intergenic_variant - - - - - - rs6527540 X:36169660 G ENSESTG00000019449 ENSESTT00000048917 Transcript intron_variant - - - - - - rs28735426 X:36806309 C - - - intergenic_variant - - - - - - rs28785181 X:36843374 T - - - intergenic_variant - - - - - - rs28809609 X:36871231 C - - - intergenic_variant - - - - - - rs5917622 X:37306146 A 5638 NM_001173489.1 Transcript intron_variant - - - - - - rs5917622 X:37306146 A ENSESTG00000013032 ENSESTT00000032700 Transcript intron_variant - - - - - - rs5917622 X:37306146 A 5638 NM_001142395.1 Transcript intron_variant - - - - - - rs5917622 X:37306146 A 5638 NM_000950.2 Transcript intron_variant - - - - - - rs5917622 X:37306146 A 5638 NM_001173486.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4669 rs5917622 X:37306146 A CCDS14239.1 CCDS14239.1 Transcript intron_variant - - - - - - rs5917622 X:37306146 A ENSESTG00000013032 ENSESTT00000032711 Transcript intron_variant - - - - - - rs5917622 X:37306146 A ENSESTG00000013032 ENSESTT00000032703 Transcript intron_variant - - - - - - rs5917622 X:37306146 A ENSESTG00000013032 ENSESTT00000032708 Transcript intron_variant - - - - - - rs5917622 X:37306146 A 5638 NM_001173490.1 Transcript intron_variant - - - - - - rs180694709 X:37370766 A - - - intergenic_variant - - - - - - rs5917516 X:37829521 C ENSESTG00000013089 ENSESTT00000032831 Transcript intron_variant - - - - - - rs5917516 X:37829521 C ENSESTG00000013089 ENSESTT00000032818 Transcript intron_variant - - - - - - rs5917516 X:37829521 C ENSESTG00000013089 ENSESTT00000032815 Transcript intron_variant - - - - - - rs1022452 X:38532530 C ENSESTG00000026278 ENSESTT00000066449 Transcript intron_variant - - - - - - rs1022452 X:38532530 C 7102 NM_004615.3 Transcript intron_variant - - - - - - rs1022452 X:38532530 C CCDS14248.1 CCDS14248.1 Transcript intron_variant - - - - - - rs1022452 X:38532530 C ENSESTG00000026278 ENSESTT00000066500 Transcript intron_variant - - - - - - rs1022452 X:38532530 C ENSESTG00000026278 ENSESTT00000066516 Transcript intron_variant - - - - - - rs1022452 X:38532530 C ENSESTG00000026278 ENSESTT00000066531 Transcript intron_variant - - - - - - rs1022452 X:38532530 C ENSESTG00000026278 ENSESTT00000066484 Transcript intron_variant - - - - - - rs1022452 X:38532530 C ENSESTG00000026278 ENSESTT00000066469 Transcript intron_variant - - - - - - rs1022452 X:38532530 C ENSESTG00000026278 ENSESTT00000066524 Transcript intron_variant - - - - - - rs62590361 X:38759700 C - - - intergenic_variant - - - - - - rs62590387 X:38786263 C - - - intergenic_variant - - - - - - rs11266230 X:38815367 C - - - intergenic_variant - - - - - - rs62590435 X:38856283 C - - - intergenic_variant - - - - - - rs6417839 X:39002569 G - - - intergenic_variant - - - - - - rs2205522 X:39026751 C - - - intergenic_variant - - - - - - rs5917298 X:39215710 A - - - intergenic_variant - - - - - - rs4240036 X:39218862 T - - - intergenic_variant - - - - - - rs5963128 X:39354419 A - - - intergenic_variant - - - - - - rs3008905 X:39663321 G - - - intergenic_variant - - - - - - rs3008904 X:39665688 G - - - intergenic_variant - - - - - - rs5963150 X:39894662 A - - - intergenic_variant - - - - - - rs4827195 X:39964073 C - ENSR00000071351 RegulatoryFeature regulatory_region_variant - - - - - - rs4827195 X:39964073 C 54880 NM_001123383.1 Transcript intron_variant - - - - - - rs4827195 X:39964073 C ENSESTG00000027891 ENSESTT00000070191 Transcript intron_variant - - - - - - rs4827195 X:39964073 C ENSESTG00000027891 ENSESTT00000070228 Transcript intron_variant - - - - - - rs4827195 X:39964073 C 54880 NM_001123384.1 Transcript intron_variant - - - - - - rs2961395 X:40217840 G - - - intergenic_variant - - - - - - rs12844590 X:40240440 C - - - intergenic_variant - - - - - - rs2961382 X:40316205 C - - - intergenic_variant - - - - - - rs5917975 X:40333562 G - ENSR00000477568 RegulatoryFeature regulatory_region_variant - - - - - - rs5917975 X:40333562 G - - - intergenic_variant - - - - - - rs2961389 X:40341702 C - - - intergenic_variant - - - - - - rs4827214 X:40347257 A - - - intergenic_variant - - - - - - rs5963805 X:40389298 T - - - intergenic_variant - - - - - - rs5917997 X:40410483 G - - - intergenic_variant - - - - - - rs4827227 X:40582981 A ENSESTG00000027558 ENSESTT00000069935 Transcript intron_variant - - - - - - rs4827227 X:40582981 A 9282 NM_004229.3 Transcript intron_variant - - - - - - rs4827227 X:40582981 A ENSESTG00000027558 ENSESTT00000070023 Transcript intron_variant - - - - - - rs4827227 X:40582981 A ENSESTG00000027558 ENSESTT00000069966 Transcript intron_variant - - - - - - rs4827227 X:40582981 A CCDS14254.1 CCDS14254.1 Transcript intron_variant - - - - - - rs4827241 X:40677471 T - - - intergenic_variant - - - - - - rs5918052 X:40721283 T - - - intergenic_variant - - - - - - rs5963877 X:40737496 A - ENSR00000477608 RegulatoryFeature regulatory_region_variant - - - - - - rs5963877 X:40737496 A - - - intergenic_variant - - - - - - rs5918079 X:40847108 A - - - intergenic_variant - - - - - - rs5918087 X:40872073 A - - - intergenic_variant - - - - - - rs2993423 X:40874934 G - - - intergenic_variant - - - - - - rs1243787 X:40968526 T 8239 NM_001039591.2 Transcript intron_variant - - - - - - rs1243787 X:40968526 T ENSESTG00000034481 ENSESTT00000087261 Transcript intron_variant - - - - - - rs1243787 X:40968526 T ENSESTG00000024305 ENSESTT00000061429 Transcript intron_variant - - - - - - rs1243787 X:40968526 T 8239 NM_001039590.2 Transcript intron_variant - - - - - - rs1243787 X:40968526 T ENSESTG00000034481 ENSESTT00000087267 Transcript intron_variant - - - - - - rs5917433 X:41434212 G ENSESTG00000024158 ENSESTT00000061305 Transcript intron_variant - - - - - - rs5917433 X:41434212 G CCDS48094.1 CCDS48094.1 Transcript intron_variant - - - - - - rs5917433 X:41434212 G ENSESTG00000024158 ENSESTT00000061391 Transcript intron_variant - - - - - - rs5917433 X:41434212 G ENSESTG00000024158 ENSESTT00000061315 Transcript intron_variant - - - - - - rs5917433 X:41434212 G CCDS48095.1 CCDS48095.1 Transcript intron_variant - - - - - - rs5917433 X:41434212 G 8573 NM_001126054.2 Transcript intron_variant - - - - - - rs5917433 X:41434212 G ENSESTG00000024158 ENSESTT00000061311 Transcript intron_variant - - - - - - rs5917433 X:41434212 G ENSESTG00000024158 ENSESTT00000061382 Transcript intron_variant - - - - - - rs5917433 X:41434212 G CCDS14257.1 CCDS14257.1 Transcript intron_variant - - - - - - rs5917433 X:41434212 G 8573 NM_003688.3 Transcript intron_variant - - - - - - rs5917433 X:41434212 G ENSESTG00000024158 ENSESTT00000061404 Transcript intron_variant - - - - - - rs5917433 X:41434212 G ENSESTG00000024158 ENSESTT00000061344 Transcript intron_variant - - - - - - rs5917433 X:41434212 G ENSESTG00000024158 ENSESTT00000061397 Transcript intron_variant - - - - - - rs5917433 X:41434212 G 8573 NM_001126055.2 Transcript intron_variant - - - - - - rs4827283 X:41510038 A ENSESTG00000024158 ENSESTT00000061305 Transcript intron_variant - - - - - - rs4827283 X:41510038 A CCDS48094.1 CCDS48094.1 Transcript intron_variant - - - - - - rs4827283 X:41510038 A ENSESTG00000024158 ENSESTT00000061391 Transcript intron_variant - - - - - - rs4827283 X:41510038 A ENSESTG00000024158 ENSESTT00000061315 Transcript intron_variant - - - - - - rs4827283 X:41510038 A CCDS48095.1 CCDS48095.1 Transcript intron_variant - - - - - - rs4827283 X:41510038 A 8573 NM_001126054.2 Transcript intron_variant - - - - - - rs4827283 X:41510038 A ENSESTG00000024158 ENSESTT00000061311 Transcript intron_variant - - - - - - rs4827283 X:41510038 A ENSESTG00000024158 ENSESTT00000061382 Transcript intron_variant - - - - - - rs4827283 X:41510038 A CCDS14257.1 CCDS14257.1 Transcript intron_variant - - - - - - rs4827283 X:41510038 A 8573 NM_003688.3 Transcript intron_variant - - - - - - rs4827283 X:41510038 A ENSESTG00000024158 ENSESTT00000061404 Transcript intron_variant - - - - - - rs4827283 X:41510038 A ENSESTG00000024158 ENSESTT00000061344 Transcript intron_variant - - - - - - rs4827283 X:41510038 A ENSESTG00000024158 ENSESTT00000061397 Transcript intron_variant - - - - - - rs4827283 X:41510038 A 8573 NM_001126055.2 Transcript intron_variant - - - - - - rs5918240 X:41633084 T ENSESTG00000024158 ENSESTT00000061305 Transcript intron_variant - - - - - - rs5918240 X:41633084 T CCDS48094.1 CCDS48094.1 Transcript intron_variant - - - - - - rs5918240 X:41633084 T ENSESTG00000024158 ENSESTT00000061315 Transcript intron_variant - - - - - - rs5918240 X:41633084 T CCDS48095.1 CCDS48095.1 Transcript intron_variant - - - - - - rs5918240 X:41633084 T 8573 NM_001126054.2 Transcript intron_variant - - - - - - rs5918240 X:41633084 T ENSESTG00000024158 ENSESTT00000061311 Transcript intron_variant - - - - - - rs5918240 X:41633084 T CCDS14257.1 CCDS14257.1 Transcript intron_variant - - - - - - rs5918240 X:41633084 T ENSESTG00000024158 ENSESTT00000061072 Transcript intron_variant - - - - - - rs5918240 X:41633084 T 8573 NM_003688.3 Transcript intron_variant - - - - - - rs5918240 X:41633084 T ENSESTG00000024158 ENSESTT00000061344 Transcript intron_variant - - - - - - rs5918240 X:41633084 T 8573 NM_001126055.2 Transcript intron_variant - - - - - - rs947683 X:41841043 G - ENSR00000477765 RegulatoryFeature regulatory_region_variant - - - - - - rs947683 X:41841043 G - - - intergenic_variant - - - - - - rs1935627 X:41876852 C - - - intergenic_variant - - - - - - rs5964076 X:41920701 T - - - intergenic_variant - - - - - - rs763054 X:41988071 C - - - intergenic_variant - - - - - - rs5918296 X:41999155 A - - - intergenic_variant - - - - - - rs5918302 X:42038711 G - - - intergenic_variant - - - - - - rs5918303 X:42055196 C - - - intergenic_variant - - - - - - rs4265351 X:42104439 G - - - intergenic_variant - - - - - - rs5964145 X:42221670 G - - - intergenic_variant - - - - - - rs4827070 X:42226325 G - - - intergenic_variant - - - - - - rs4827320 X:42617822 T ENSESTG00000010617 ENSESTT00000026562 Transcript upstream_gene_variant - - - - - - DISTANCE=2690 rs2040421 X:42667311 A - - - intergenic_variant - - - - - - rs2040417 X:42667597 G - - - intergenic_variant - - - - - - rs5950928 X:42675742 C - - - intergenic_variant - - - - - - rs763057 X:42695394 G - - - intergenic_variant - - - - - - rs4986531 X:42716382 G - - - intergenic_variant - - - - - - rs5991467 X:42716790 G - - - intergenic_variant - - - - - - rs2410975 X:42738017 C - - - intergenic_variant - - - - - - rs205823 X:42785211 C - - - intergenic_variant - - - - - - rs205848 X:42792029 T - - - intergenic_variant - - - - - - rs205858 X:42795705 G - - - intergenic_variant - - - - - - rs5950979 X:43069775 A - - - intergenic_variant - - - - - - rs5950989 X:43094443 C - - - intergenic_variant - - - - - - rs5950902 X:43190202 G - - - intergenic_variant - - - - - - rs1181287 X:43368147 T - - - intergenic_variant - - - - - - rs1181251 X:43741616 C - ENSR00000477879 RegulatoryFeature regulatory_region_variant - - - - - - rs1181251 X:43741616 C CCDS14261.1 CCDS14261.1 Transcript upstream_gene_variant - - - - - - DISTANCE=71 rs1181251 X:43741616 C 4129 NM_000898.4 Transcript 5_prime_UTR_variant 106 - - - - - rs1181251 X:43741616 C ENSESTG00000010758 ENSESTT00000026936 Transcript upstream_gene_variant - - - - - - DISTANCE=22 rs400008 X:43851068 A - - - intergenic_variant - - - - - - rs209757 X:43860558 A - - - intergenic_variant - - - - - - rs209769 X:43884082 G - - - intergenic_variant - - - - - - rs287775 X:43927093 A - - - intergenic_variant - - - - - - rs4824508 X:44453657 A - - - intergenic_variant - - - - - - rs431457 X:44544185 A - - - intergenic_variant - - - - - - rs5905445 X:45163346 A - - - intergenic_variant - - - - - - rs1207295 X:46039651 T - ENSR00001489759 RegulatoryFeature regulatory_region_variant - - - - - - rs1207295 X:46039651 T - - - intergenic_variant - - - - - - rs6521119 X:46402916 G - ENSR00001031465 RegulatoryFeature regulatory_region_variant - - - - - - rs6521119 X:46402916 G 641339 NM_001146291.1 Transcript intron_variant - - - - - - rs6521119 X:46402916 G 401588 NR_015378.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2009 rs6521119 X:46402916 G 641339 NM_001039891.2 Transcript intron_variant - - - - - - rs6521119 X:46402916 G CCDS48099.1 CCDS48099.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1394 rs6521119 X:46402916 G 641339 NM_001190417.1 Transcript intron_variant - - - - - - rs6521119 X:46402916 G ENSESTG00000023762 ENSESTT00000059940 Transcript intron_variant - - - - - - rs6521119 X:46402916 G ENSESTG00000023762 ENSESTT00000059972 Transcript intron_variant - - - - - - rs6521119 X:46402916 G ENSESTG00000023762 ENSESTT00000059951 Transcript intron_variant - - - - - - rs6521119 X:46402916 G ENSESTG00000023588 ENSESTT00000059496 Transcript upstream_gene_variant - - - - - - DISTANCE=2028 rs6521119 X:46402916 G ENSESTG00000023588 ENSESTT00000059475 Transcript upstream_gene_variant - - - - - - DISTANCE=2014 rs6521119 X:46402916 G CCDS55406.1 CCDS55406.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1394 rs3135215 X:46829409 T - ENSR00000478235 RegulatoryFeature regulatory_region_variant - - - - - - rs3135215 X:46829409 T 9767 NM_014735.3 Transcript intron_variant - - - - - - rs3135215 X:46829409 T 9767 NM_001077445.1 Transcript intron_variant - - - - - - rs3135215 X:46829409 T ENSESTG00000023630 ENSESTT00000059700 Transcript intron_variant - - - - - - rs3135215 X:46829409 T ENSESTG00000023630 ENSESTT00000059712 Transcript intron_variant - - - - - - rs3135215 X:46829409 T ENSESTG00000023630 ENSESTT00000059679 Transcript intron_variant - - - - - - rs62591304 X:46865045 C 9767 NM_014735.3 Transcript intron_variant - - - - - - rs62591304 X:46865045 C 9767 NM_001077445.1 Transcript intron_variant - - - - - - rs62591304 X:46865045 C ENSESTG00000023630 ENSESTT00000059700 Transcript intron_variant - - - - - - rs62591304 X:46865045 C CCDS14271.1 CCDS14271.1 Transcript intron_variant - - - - - - rs62591304 X:46865045 C ENSESTG00000023630 ENSESTT00000059712 Transcript intron_variant - - - - - - rs62591304 X:46865045 C ENSESTG00000015558 ENSESTT00000038988 Transcript intron_variant - - - - - - rs62591304 X:46865045 C ENSESTG00000023630 ENSESTT00000059679 Transcript intron_variant - - - - - - rs5906315 X:46907921 C 9767 NM_014735.3 Transcript intron_variant - - - - - - rs5906315 X:46907921 C 9767 NM_001077445.1 Transcript intron_variant - - - - - - rs5906315 X:46907921 C CCDS14271.1 CCDS14271.1 Transcript intron_variant - - - - - - rs5906357 X:47080994 C ENSESTG00000015821 ENSESTT00000039860 Transcript upstream_gene_variant - - - - - - DISTANCE=537 rs5906357 X:47080994 C CCDS14276.1 CCDS14276.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1963 rs5906357 X:47080994 C CCDS48101.1 CCDS48101.1 Transcript intron_variant - - - - - - rs5906357 X:47080994 C 5127 NM_001170460.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1423 rs5906357 X:47080994 C 5127 NM_033018.3 Transcript intron_variant - - - - - - rs5906357 X:47080994 C CCDS55408.1 CCDS55408.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1501 rs5906357 X:47080994 C 5127 NM_006201.4 Transcript intron_variant - - - - - - rs5906357 X:47080994 C ENSESTG00000015821 ENSESTT00000039847 Transcript intron_variant - - - - - - rs5906357 X:47080994 C ENSESTG00000015821 ENSESTT00000039871 Transcript upstream_gene_variant - - - - - - DISTANCE=4682 rs3005645 X:47132136 C - - - intergenic_variant - - - - - - rs3005647 X:47133151 C - - - intergenic_variant - - - - - - rs3005649 X:47133661 G - - - intergenic_variant - - - - - - rs5906377 X:47167270 G - - - intergenic_variant - - - - - - rs3005662 X:47169815 C - - - intergenic_variant - - - - - - rs2854418 X:47420745 C - ENSR00000478290 RegulatoryFeature regulatory_region_variant - - - - - - rs2854418 X:47420745 C 369 NM_001654.4 Transcript intron_variant - - - - - - rs2854418 X:47420745 C CCDS35232.1 CCDS35232.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1622 rs2854418 X:47420745 C ENSESTG00000016013 ENSESTT00000040279 Transcript intron_variant - - - - - - rs2854418 X:47420745 C 369 NM_001256196.1 Transcript intron_variant - - - - - - rs2854418 X:47420745 C CCDS59164.1 CCDS59164.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1622 rs2854418 X:47420745 C ENSESTG00000016013 ENSESTT00000040286 Transcript intron_variant - - - - - - rs2854418 X:47420745 C 369 NM_001256197.1 Transcript intron_variant - - - - - - rs5906451 X:47547080 C - - - intergenic_variant - - - - - - rs109244 X:47886034 T - ENSR00000660499 RegulatoryFeature regulatory_region_variant - - - - - - rs109244 X:47886034 T ENSESTG00000034043 ENSESTT00000086036 Transcript intron_variant - - - - - - rs5906546 X:48027012 A - - - intergenic_variant - - - - - - rs6609708 X:48186386 C ENSESTG00000034445 ENSESTT00000087141 Transcript intron_variant - - - - - - rs6608801 X:48217723 T ENSESTG00000034445 ENSESTT00000087135 Transcript upstream_gene_variant - - - - - - DISTANCE=1581 rs6608801 X:48217723 T ENSESTG00000034445 ENSESTT00000087141 Transcript upstream_gene_variant - - - - - - DISTANCE=1613 rs6608801 X:48217723 T 10214 NM_021014.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1581 rs6608801 X:48217723 T CCDS35239.1 CCDS35239.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3039 rs6608801 X:48217723 T CCDS14291.1 CCDS14291.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3039 rs6608801 X:48217723 T 10214 NM_175711.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1581 rs3014645 X:48289058 G - - - intergenic_variant - - - - - - rs7876401 X:48311832 A - - - intergenic_variant - - - - - - rs235842 X:48460314 G 64743 NM_001166426.1 Transcript missense_variant 1814 698 233 H/R cAt/cGt - rs235842 X:48460314 G ENSESTG00000034251 ENSESTT00000086578 Transcript downstream_gene_variant - - - - - - DISTANCE=49 rs235842 X:48460314 G CCDS14302.1 CCDS14302.1 Transcript missense_variant 974 974 325 H/R cAt/cGt - PolyPhen=benign;SIFT=tolerated rs235842 X:48460314 G 64743 NM_017883.4 Transcript missense_variant 1479 974 325 H/R cAt/cGt - PolyPhen=benign;SIFT=tolerated rs235842 X:48460314 G 64743 NR_029427.1 Transcript non_coding_exon_variant,nc_transcript_variant 1445 - - - - - rs235842 X:48460314 G ENSESTG00000034253 ENSESTT00000086618 Transcript upstream_gene_variant - - - - - - DISTANCE=17 rs4824727 X:48601178 G ENSESTG00000034416 ENSESTT00000087055 Transcript upstream_gene_variant - - - - - - DISTANCE=777 rs4824728 X:48606111 G - - - intergenic_variant - - - - - - rs28718016 X:48806587 C ENSESTG00000033308 ENSESTT00000084204 Transcript intron_variant - - - - - - rs28718016 X:48806587 C ENSESTG00000033308 ENSESTT00000084199 Transcript intron_variant - - - - - - rs28718016 X:48806587 C CCDS48104.1 CCDS48104.1 Transcript intron_variant - - - - - - rs28718016 X:48806587 C 55593 NM_001136158.1 Transcript intron_variant - - - - - - rs28718016 X:48806587 C ENSESTG00000033308 ENSESTT00000084198 Transcript intron_variant - - - - - - rs28718016 X:48806587 C ENSESTG00000033308 ENSESTT00000084181 Transcript intron_variant - - - - - - rs28718016 X:48806587 C 55593 NM_001136157.1 Transcript intron_variant - - - - - - rs28718016 X:48806587 C ENSESTG00000033308 ENSESTT00000084216 Transcript intron_variant - - - - - - rs28718016 X:48806587 C ENSESTG00000033308 ENSESTT00000084213 Transcript intron_variant - - - - - - rs28718016 X:48806587 C CCDS14313.1 CCDS14313.1 Transcript intron_variant - - - - - - rs28718016 X:48806587 C 55593 NM_001136159.1 Transcript intron_variant - - - - - - rs28718016 X:48806587 C ENSESTG00000033308 ENSESTT00000084194 Transcript intron_variant - - - - - - rs28718016 X:48806587 C 55593 NM_017602.3 Transcript intron_variant - - - - - - rs7050095 X:48988518 C - - - intergenic_variant - - - - - - rs5906744 X:49021256 G ENSESTG00000032790 ENSESTT00000082854 Transcript missense_variant 237 158 53 H/R cAt/cGt - rs5906744 X:49021256 G 79917 NM_024859.2 Transcript missense_variant 382 335 112 H/R cAt/cGt - PolyPhen=benign;SIFT=tolerated rs5906744 X:49021256 G 79917 NM_001099681.1 Transcript intron_variant - - - - - - rs5906744 X:49021256 G CCDS48106.1 CCDS48106.1 Transcript missense_variant 335 335 112 H/R cAt/cGt - PolyPhen=benign;SIFT=tolerated rs5906744 X:49021256 G ENSESTG00000032790 ENSESTT00000082864 Transcript intron_variant - - - - - - rs5906744 X:49021256 G ENSESTG00000032790 ENSESTT00000082869 Transcript missense_variant 173 173 58 H/R cAt/cGt - PolyPhen=benign;SIFT=tolerated rs5906744 X:49021256 G ENSESTG00000032790 ENSESTT00000082849 Transcript missense_variant 164 164 55 H/R cAt/cGt - rs5906744 X:49021256 G CCDS48107.1 CCDS48107.1 Transcript intron_variant - - - - - - rs5906744 X:49021256 G ENSESTG00000032790 ENSESTT00000082877 Transcript intron_variant - - - - - - rs5906744 X:49021256 G ENSESTG00000032790 ENSESTT00000082858 Transcript intron_variant - - - - - - rs5906744 X:49021256 G 79917 NM_001099682.1 Transcript intron_variant - - - - - - rs5906744 X:49021256 G 79917 NM_001099680.1 Transcript missense_variant 869 134 45 H/R cAt/cGt - rs5905720 X:49021537 C ENSESTG00000032790 ENSESTT00000082854 Transcript missense_variant 419 340 114 V/L Gtc/Ctc - rs5905720 X:49021537 C 79917 NM_024859.2 Transcript missense_variant 564 517 173 V/L Gtc/Ctc - PolyPhen=benign;SIFT=tolerated rs5905720 X:49021537 C 79917 NM_001099681.1 Transcript missense_variant 336 289 97 V/L Gtc/Ctc - PolyPhen=benign;SIFT=tolerated rs5905720 X:49021537 C CCDS48106.1 CCDS48106.1 Transcript missense_variant 517 517 173 V/L Gtc/Ctc - PolyPhen=benign;SIFT=tolerated rs5905720 X:49021537 C ENSESTG00000032790 ENSESTT00000082864 Transcript synonymous_variant 408 39 13 T acG/acC - rs5905720 X:49021537 C ENSESTG00000032790 ENSESTT00000082869 Transcript missense_variant 355 355 119 V/L Gtc/Ctc - PolyPhen=benign;SIFT=tolerated rs5905720 X:49021537 C ENSESTG00000032790 ENSESTT00000082849 Transcript missense_variant 346 346 116 V/L Gtc/Ctc - rs5905720 X:49021537 C CCDS48107.1 CCDS48107.1 Transcript missense_variant 289 289 97 V/L Gtc/Ctc - PolyPhen=benign;SIFT=tolerated rs5905720 X:49021537 C ENSESTG00000032790 ENSESTT00000082877 Transcript missense_variant 176 133 45 V/L Gtc/Ctc - rs5905720 X:49021537 C ENSESTG00000032790 ENSESTT00000082858 Transcript missense_variant 408 154 52 V/L Gtc/Ctc - rs5905720 X:49021537 C 79917 NM_001099682.1 Transcript missense_variant 336 289 97 V/L Gtc/Ctc - rs5905720 X:49021537 C 79917 NM_001099680.1 Transcript missense_variant 1051 316 106 V/L Gtc/Ctc - rs4824462 X:49022700 C - ENSR00000260124 RegulatoryFeature regulatory_region_variant - - - - - - rs4824462 X:49022700 C ENSESTG00000032790 ENSESTT00000082854 Transcript downstream_gene_variant - - - - - - DISTANCE=997 rs4824462 X:49022700 C 79917 NM_024859.2 Transcript missense_variant 1014 967 323 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs4824462 X:49022700 C 79917 NM_001099681.1 Transcript missense_variant 786 739 247 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs4824462 X:49022700 C CCDS48106.1 CCDS48106.1 Transcript missense_variant 967 967 323 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs4824462 X:49022700 C ENSESTG00000032790 ENSESTT00000082864 Transcript downstream_gene_variant - - - - - - DISTANCE=181 rs4824462 X:49022700 C ENSESTG00000032790 ENSESTT00000082869 Transcript downstream_gene_variant - - - - - - DISTANCE=148 rs4824462 X:49022700 C ENSESTG00000032790 ENSESTT00000082849 Transcript missense_variant 796 796 266 F/L Ttc/Ctc - rs4824462 X:49022700 C CCDS48107.1 CCDS48107.1 Transcript missense_variant 739 739 247 F/L Ttc/Ctc - PolyPhen=benign;SIFT=tolerated rs4824462 X:49022700 C ENSESTG00000032790 ENSESTT00000082877 Transcript downstream_gene_variant - - - - - - DISTANCE=181 rs4824462 X:49022700 C ENSESTG00000032790 ENSESTT00000082858 Transcript missense_variant 858 604 202 F/L Ttc/Ctc - rs4824462 X:49022700 C 79917 NM_001099682.1 Transcript missense_variant 771 724 242 F/L Ttc/Ctc - rs4824462 X:49022700 C 79917 NM_001099680.1 Transcript missense_variant 1486 751 251 F/L Ttc/Ctc - rs6610009 X:49435963 C - - - intergenic_variant - - - - - - rs179572 X:49681425 G - - - intergenic_variant - - - - - - rs151264 X:49683824 G 1184 NM_001127898.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3401 rs151264 X:49683824 G ENSESTG00000032965 ENSESTT00000083329 Transcript upstream_gene_variant - - - - - - DISTANCE=3487 rs151264 X:49683824 G ENSESTG00000032965 ENSESTT00000083322 Transcript upstream_gene_variant - - - - - - DISTANCE=3451 rs151264 X:49683824 G ENSESTG00000032965 ENSESTT00000083317 Transcript upstream_gene_variant - - - - - - DISTANCE=3404 rs151264 X:49683824 G 1184 NM_001127899.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3401 rs179573 X:49685141 C 1184 NM_001127898.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2084 rs179573 X:49685141 C ENSESTG00000032965 ENSESTT00000083329 Transcript upstream_gene_variant - - - - - - DISTANCE=2170 rs179573 X:49685141 C ENSESTG00000032965 ENSESTT00000083322 Transcript upstream_gene_variant - - - - - - DISTANCE=2134 rs179573 X:49685141 C ENSESTG00000032965 ENSESTT00000083317 Transcript upstream_gene_variant - - - - - - DISTANCE=2087 rs179573 X:49685141 C 1184 NM_001127899.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2084 rs179573 X:49685141 C CCDS48115.1 CCDS48115.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4768 rs179574 X:49685202 C 1184 NM_001127898.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2023 rs179574 X:49685202 C ENSESTG00000032965 ENSESTT00000083329 Transcript upstream_gene_variant - - - - - - DISTANCE=2109 rs179574 X:49685202 C ENSESTG00000032965 ENSESTT00000083322 Transcript upstream_gene_variant - - - - - - DISTANCE=2073 rs179574 X:49685202 C ENSESTG00000032965 ENSESTT00000083317 Transcript upstream_gene_variant - - - - - - DISTANCE=2026 rs179574 X:49685202 C 1184 NM_001127899.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2023 rs179574 X:49685202 C CCDS48115.1 CCDS48115.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4707 rs151265 X:49687616 C - ENSR00001031004 RegulatoryFeature regulatory_region_variant - - - - - - rs151265 X:49687616 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs151265 X:49687616 C ENSESTG00000032965 ENSESTT00000083329 Transcript intron_variant - - - - - - rs151265 X:49687616 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs151265 X:49687616 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs151265 X:49687616 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs151265 X:49687616 C CCDS48115.1 CCDS48115.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2293 rs151266 X:49689082 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs151266 X:49689082 C ENSESTG00000032965 ENSESTT00000083329 Transcript intron_variant - - - - - - rs151266 X:49689082 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs151266 X:49689082 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs151266 X:49689082 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs151266 X:49689082 C CCDS48115.1 CCDS48115.1 Transcript upstream_gene_variant - - - - - - DISTANCE=827 rs149257 X:49694076 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs149257 X:49694076 G ENSESTG00000032965 ENSESTT00000083329 Transcript downstream_gene_variant - - - - - - DISTANCE=4150 rs149257 X:49694076 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs149257 X:49694076 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs149257 X:49694076 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs149257 X:49694076 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs449483 X:49697782 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs449483 X:49697782 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs449483 X:49697782 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs449483 X:49697782 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs449483 X:49697782 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs451514 X:49697786 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs451514 X:49697786 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs451514 X:49697786 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs451514 X:49697786 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs451514 X:49697786 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs383511 X:49700757 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs383511 X:49700757 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs383511 X:49700757 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs383511 X:49700757 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs383511 X:49700757 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs453601 X:49704890 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs453601 X:49704890 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs453601 X:49704890 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs453601 X:49704890 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs453601 X:49704890 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs445222 X:49704893 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs445222 X:49704893 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs445222 X:49704893 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs445222 X:49704893 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs445222 X:49704893 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232749 X:49705238 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232749 X:49705238 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232749 X:49705238 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232749 X:49705238 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232749 X:49705238 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs381274 X:49706674 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs381274 X:49706674 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs381274 X:49706674 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs381274 X:49706674 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs381274 X:49706674 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232752 X:49711241 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232752 X:49711241 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232752 X:49711241 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232752 X:49711241 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232752 X:49711241 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232754 X:49712744 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232754 X:49712744 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232754 X:49712744 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232754 X:49712744 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232754 X:49712744 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232756 X:49718702 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232756 X:49718702 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232756 X:49718702 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232756 X:49718702 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232756 X:49718702 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs179796 X:49719846 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs179796 X:49719846 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs179796 X:49719846 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs179796 X:49719846 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs179796 X:49719846 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232757 X:49726008 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232757 X:49726008 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232757 X:49726008 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232757 X:49726008 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232757 X:49726008 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232760 X:49734376 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232760 X:49734376 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232760 X:49734376 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232760 X:49734376 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232760 X:49734376 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232762 X:49737465 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232762 X:49737465 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232762 X:49737465 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232762 X:49737465 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232762 X:49737465 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232763 X:49743426 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232763 X:49743426 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232763 X:49743426 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232763 X:49743426 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232763 X:49743426 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232765 X:49749263 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232765 X:49749263 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232765 X:49749263 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232765 X:49749263 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232765 X:49749263 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs232766 X:49754201 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs232766 X:49754201 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs232766 X:49754201 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs232766 X:49754201 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs232766 X:49754201 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs396009 X:49756193 T 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs396009 X:49756193 T ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs396009 X:49756193 T ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs396009 X:49756193 T 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs396009 X:49756193 T CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs413497 X:49757187 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs413497 X:49757187 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs413497 X:49757187 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs413497 X:49757187 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs413497 X:49757187 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs179823 X:49760522 G - ENSR00001489934 RegulatoryFeature regulatory_region_variant - - - - - - rs179823 X:49760522 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs179823 X:49760522 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs179823 X:49760522 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs179823 X:49760522 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs179823 X:49760522 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs179825 X:49763893 C - ENSR00000478478 RegulatoryFeature regulatory_region_variant - - - - - - rs179825 X:49763893 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs179825 X:49763893 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs179825 X:49763893 C 693124 NR_030241.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3861 rs179825 X:49763893 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs179825 X:49763893 C 406964 NR_029708.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4216 rs179825 X:49763893 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs179825 X:49763893 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs179826 X:49763937 C - ENSR00000478478 RegulatoryFeature regulatory_region_variant - - - - - - rs179826 X:49763937 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs179826 X:49763937 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs179826 X:49763937 C 693124 NR_030241.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3817 rs179826 X:49763937 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs179826 X:49763937 C 406964 NR_029708.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4172 rs179826 X:49763937 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs179826 X:49763937 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs179827 X:49763955 C - ENSR00000478478 RegulatoryFeature regulatory_region_variant - - - - - - rs179827 X:49763955 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs179827 X:49763955 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs179827 X:49763955 C 693124 NR_030241.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3799 rs179827 X:49763955 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs179827 X:49763955 C 406964 NR_029708.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4154 rs179827 X:49763955 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs179827 X:49763955 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs179828 X:49763983 C - ENSR00000478478 RegulatoryFeature regulatory_region_variant - - - - - - rs179828 X:49763983 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs179828 X:49763983 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs179828 X:49763983 C 693124 NR_030241.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3771 rs179828 X:49763983 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs179828 X:49763983 C 406964 NR_029708.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4126 rs179828 X:49763983 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs179828 X:49763983 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs149259 X:49767904 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs149259 X:49767904 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs149259 X:49767904 G 693124 NR_030241.1 Transcript downstream_gene_variant - - - - - - DISTANCE=60 rs149259 X:49767904 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs149259 X:49767904 G 406964 NR_029708.1 Transcript upstream_gene_variant - - - - - - DISTANCE=205 rs149259 X:49767904 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs149259 X:49767904 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs151261 X:49768449 G 574502 NR_030224.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4590 rs151261 X:49768449 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs151261 X:49768449 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs151261 X:49768449 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs151261 X:49768449 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs151261 X:49768449 G 693124 NR_030241.1 Transcript downstream_gene_variant - - - - - - DISTANCE=605 rs151261 X:49768449 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs151261 X:49768449 G 406964 NR_029708.1 Transcript downstream_gene_variant - - - - - - DISTANCE=255 rs151262 X:49768621 G 574502 NR_030224.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4418 rs151262 X:49768621 G 574030 NR_029850.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4951 rs151262 X:49768621 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs151262 X:49768621 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs151262 X:49768621 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs151262 X:49768621 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs151262 X:49768621 G 693124 NR_030241.1 Transcript downstream_gene_variant - - - - - - DISTANCE=777 rs151262 X:49768621 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs151262 X:49768621 G 406964 NR_029708.1 Transcript downstream_gene_variant - - - - - - DISTANCE=427 rs151263 X:49769888 G 574502 NR_030224.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3151 rs151263 X:49769888 G 574030 NR_029850.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3684 rs151263 X:49769888 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs151263 X:49769888 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs151263 X:49769888 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs151263 X:49769888 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs151263 X:49769888 G 574503 NR_030225.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4442 rs151263 X:49769888 G 693124 NR_030241.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2044 rs151263 X:49769888 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs151263 X:49769888 G 406964 NR_029708.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1694 rs149260 X:49771612 C 574502 NR_030224.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1427 rs149260 X:49771612 C 574030 NR_029850.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1960 rs149260 X:49771612 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs149260 X:49771612 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs149260 X:49771612 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs149260 X:49771612 C 100422911 NR_036257.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3668 rs149260 X:49771612 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs149260 X:49771612 C 574503 NR_030225.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2718 rs149260 X:49771612 C 693124 NR_030241.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3768 rs149260 X:49771612 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs149260 X:49771612 C 406964 NR_029708.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3418 rs151260 X:49772536 G 574502 NR_030224.1 Transcript upstream_gene_variant - - - - - - DISTANCE=503 rs151260 X:49772536 G 574030 NR_029850.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1036 rs151260 X:49772536 G 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs151260 X:49772536 G CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs151260 X:49772536 G 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs151260 X:49772536 G 100422911 NR_036257.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2744 rs151260 X:49772536 G ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs151260 X:49772536 G 574503 NR_030225.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1794 rs151260 X:49772536 G 693124 NR_030241.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4692 rs151260 X:49772536 G ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs151260 X:49772536 G 406964 NR_029708.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4342 rs149596 X:49773805 C 574502 NR_030224.1 Transcript downstream_gene_variant - - - - - - DISTANCE=683 rs149596 X:49773805 C 574030 NR_029850.1 Transcript downstream_gene_variant - - - - - - DISTANCE=169 rs149596 X:49773805 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs149596 X:49773805 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs149596 X:49773805 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs149596 X:49773805 C 100422911 NR_036257.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1475 rs149596 X:49773805 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs149596 X:49773805 C 574503 NR_030225.1 Transcript upstream_gene_variant - - - - - - DISTANCE=525 rs149596 X:49773805 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs149596 X:49773805 C 724030 NR_030397.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4044 rs179831 X:49778334 C 574030 NR_029850.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4698 rs179831 X:49778334 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs179831 X:49778334 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs179831 X:49778334 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs179831 X:49778334 C 100422911 NR_036257.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2976 rs179831 X:49778334 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs179831 X:49778334 C 574503 NR_030225.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3921 rs179831 X:49778334 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs179831 X:49778334 C 574504 NR_030226.1 Transcript upstream_gene_variant - - - - - - DISTANCE=872 rs179831 X:49778334 C 724030 NR_030397.1 Transcript downstream_gene_variant - - - - - - DISTANCE=389 rs179832 X:49780728 C 1184 NM_001127898.1 Transcript intron_variant - - - - - - rs179832 X:49780728 C ENSESTG00000032965 ENSESTT00000083322 Transcript intron_variant - - - - - - rs179832 X:49780728 C ENSESTG00000032965 ENSESTT00000083317 Transcript intron_variant - - - - - - rs179832 X:49780728 C 574504 NR_030226.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1437 rs179832 X:49780728 C 724030 NR_030397.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2783 rs179832 X:49780728 C 1184 NM_001127899.1 Transcript intron_variant - - - - - - rs179832 X:49780728 C CCDS48115.1 CCDS48115.1 Transcript intron_variant - - - - - - rs5915230 X:50112247 C 139189 NM_001013742.2 Transcript intron_variant - - - - - - rs5915230 X:50112247 C ENSESTG00000022848 ENSESTT00000057605 Transcript intron_variant - - - - - - rs5915230 X:50112247 C ENSESTG00000022793 ENSESTT00000057474 Transcript downstream_gene_variant - - - - - - DISTANCE=3079 rs4440747 X:50683267 T - - - intergenic_variant - - - - - - rs6614652 X:50911002 C - - - intergenic_variant - - - - - - rs1276792 X:50944718 A - - - intergenic_variant - - - - - - rs5951090 X:51643018 G - ENSR00001489985 RegulatoryFeature regulatory_region_variant - - - - - - rs5951090 X:51643018 G 9500 NM_001005332.1 Transcript intron_variant - - - - - - rs5951090 X:51643018 G 9500 NM_001005333.1 Transcript intron_variant - - - - - - rs5951090 X:51643018 G ENSESTG00000033516 ENSESTT00000084830 Transcript intron_variant - - - - - - rs5951090 X:51643018 G 9500 NM_006986.3 Transcript intron_variant - - - - - - rs5951090 X:51643018 G CCDS14337.1 CCDS14337.1 Transcript intron_variant - - - - - - rs5951090 X:51643018 G CCDS35279.1 CCDS35279.1 Transcript intron_variant - - - - - - rs5991755 X:51690666 A - - - intergenic_variant - - - - - - rs9306589 X:51876880 C - - - intergenic_variant - - - - - - rs5991833 X:53049166 A - - - intergenic_variant - - - - - - rs645919 X:53521636 G - - - intergenic_variant - - - - - - rs2456903 X:53684651 G CCDS35301.1 CCDS35301.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3600 rs2456903 X:53684651 G 10075 NM_031407.5 Transcript intron_variant - - - - - - rs2456903 X:53684651 G ENSESTG00000034015 ENSESTT00000085998 Transcript intron_variant - - - - - - rs2333864 X:53713640 C - ENSR00000478683 RegulatoryFeature regulatory_region_variant - - - - - - rs2333864 X:53713640 C ENSESTG00000034015 ENSESTT00000085974 Transcript missense_variant 58 50 17 T/R aCg/aGg - rs2333864 X:53713640 C 10075 NM_031407.5 Transcript 5_prime_UTR_variant 58 - - - - - rs2333864 X:53713640 C ENSESTG00000034015 ENSESTT00000085998 Transcript upstream_gene_variant - - - - - - DISTANCE=2544 rs1894546 X:54198047 G - ENSR00001490054 RegulatoryFeature regulatory_region_variant - - - - - - rs1894546 X:54198047 G CCDS14356.1 CCDS14356.1 Transcript intron_variant - - - - - - rs1894546 X:54198047 G 54954 NM_198456.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2175 rs1894546 X:54198047 G CCDS55421.1 CCDS55421.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2515 rs1894546 X:54198047 G 54954 NM_017848.4 Transcript intron_variant - - - - - - rs2495783 X:54209387 G CCDS14356.1 CCDS14356.1 Transcript missense_variant 245 245 82 I/T aTt/aCt - PolyPhen=unknown;SIFT=tolerated rs2495783 X:54209387 G 54954 NM_198456.1 Transcript missense_variant 328 245 82 I/T aTt/aCt - PolyPhen=unknown;SIFT=tolerated rs2495783 X:54209387 G CCDS55421.1 CCDS55421.1 Transcript missense_variant 245 245 82 I/T aTt/aCt - PolyPhen=unknown;SIFT=tolerated rs2495783 X:54209387 G 54954 NM_017848.4 Transcript missense_variant 328 245 82 I/T aTt/aCt - PolyPhen=unknown;SIFT=tolerated rs2495786 X:54227094 C 65267 NM_020922.4 Transcript intron_variant - - - - - - rs2495786 X:54227094 C CCDS35302.1 CCDS35302.1 Transcript intron_variant - - - - - - rs2495786 X:54227094 C CCDS14357.1 CCDS14357.1 Transcript intron_variant - - - - - - rs2495786 X:54227094 C ENSESTG00000030438 ENSESTT00000076626 Transcript intron_variant - - - - - - rs2495786 X:54227094 C 65267 NM_001002838.3 Transcript intron_variant - - - - - - rs6521756 X:54386292 C 65267 NM_020922.4 Transcript upstream_gene_variant - - - - - - DISTANCE=1854 rs6521756 X:54386292 C 65267 NM_001002838.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1854 rs5961060 X:54419843 A - - - intergenic_variant - - - - - - rs5960409 X:55234553 C - - - intergenic_variant - - - - - - rs6417945 X:56386893 A - - - intergenic_variant - - - - - - rs6612529 X:56395921 T - - - intergenic_variant - - - - - - rs6611531 X:56606825 C - - - intergenic_variant - - - - - - rs5914747 X:56676031 A ENSESTG00000025270 ENSESTT00000063733 Transcript intron_variant - - - - - - rs1555993 X:56813995 A ENSESTG00000029686 ENSESTT00000074735 Transcript intron_variant - - - - - - rs1555993 X:56813995 A 550643 NR_015367.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs204145 X:57069704 G - - - intergenic_variant - - - - - - rs5960903 X:57136949 G - - - intergenic_variant - - - - - - rs4610890 X:57357003 G CCDS14375.1 CCDS14375.1 Transcript intron_variant - - - - - - rs4610890 X:57357003 G ENSESTG00000029724 ENSESTT00000074891 Transcript intron_variant - - - - - - rs4610890 X:57357003 G 158584 NM_174912.3 Transcript intron_variant - - - - - - rs4610890 X:57357003 G ENSESTG00000029724 ENSESTT00000074933 Transcript intron_variant - - - - - - rs4610890 X:57357003 G ENSESTG00000029724 ENSESTT00000074910 Transcript intron_variant - - - - - - rs80047674 X:57573577 C - - - intergenic_variant - - - - - - rs5947380 X:57757062 G - - - intergenic_variant - - - - - - rs6612858 X:57763662 C - - - intergenic_variant - - - - - - rs5989079 X:57816736 C - - - intergenic_variant - - - - - - rs1205831 X:57861939 C - - - intergenic_variant - - - - - - rs1211595 X:57867266 A - - - intergenic_variant - - - - - - rs5947445 X:58478074 G - - - intergenic_variant - - - - - - rs6608446 X:61921167 C - - - intergenic_variant - - - - - - rs9724048 X:62055753 T - - - intergenic_variant - - - - - - rs6418424 X:62127015 T - - - intergenic_variant - - - - - - rs6525465 X:62136078 G - - - intergenic_variant - - - - - - rs6524877 X:62205187 T - - - intergenic_variant - - - - - - rs1341711 X:62216067 C - - - intergenic_variant - - - - - - rs5918547 X:62301331 C - - - intergenic_variant - - - - - - rs191717092 X:62399542 G - ENSR00000260345 RegulatoryFeature regulatory_region_variant - - - - - - rs191717092 X:62399542 G - - - intergenic_variant - - - - - - rs1831104 X:62621282 T - - - intergenic_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088993 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088984 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088995 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088980 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088969 Transcript intron_variant - - - - - - rs5964686 X:62945209 C 23229 NM_001173479.1 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088968 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088985 Transcript intron_variant - - - - - - rs5964686 X:62945209 C CCDS35315.1 CCDS35315.1 Transcript intron_variant - - - - - - rs5964686 X:62945209 C 23229 NM_001173480.1 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088987 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088981 Transcript intron_variant - - - - - - rs5964686 X:62945209 C 23229 NM_015185.2 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088983 Transcript intron_variant - - - - - - rs5964686 X:62945209 C ENSESTG00000035222 ENSESTT00000088991 Transcript intron_variant - - - - - - rs5964686 X:62945209 C CCDS55430.1 CCDS55430.1 Transcript intron_variant - - - - - - rs5964691 X:63056553 T - - - intergenic_variant - - - - - - rs1333160 X:63162628 A - - - intergenic_variant - - - - - - rs5964755 X:63489379 G 55613 NM_017677.3 Transcript intron_variant - - - - - - rs5964755 X:63489379 G CCDS14379.1 CCDS14379.1 Transcript intron_variant - - - - - - rs5964759 X:63516107 A 55613 NM_017677.3 Transcript intron_variant - - - - - - rs5964759 X:63516107 A CCDS14379.1 CCDS14379.1 Transcript intron_variant - - - - - - rs5964359 X:63636916 C - - - intergenic_variant - - - - - - rs5964820 X:63825705 G - - - intergenic_variant - - - - - - rs5918551 X:63836031 C - - - intergenic_variant - - - - - - rs821778 X:63988535 C - - - intergenic_variant - - - - - - rs145609383 X:64158681 G 55906 NM_018684.3 Transcript intron_variant - - - - - - rs145609383 X:64158681 G ENSESTG00000023126 ENSESTT00000058394 Transcript intron_variant - - - - - - rs145609383 X:64158681 G 55906 NM_001243804.1 Transcript intron_variant - - - - - - rs145609383 X:64158681 G CCDS14380.1 CCDS14380.1 Transcript intron_variant - - - - - - rs145609383 X:64158681 G 55906 NR_045044.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs145609383 X:64158681 G 55906 NM_001178032.2 Transcript intron_variant - - - - - - rs145609383 X:64158681 G CCDS55432.1 CCDS55432.1 Transcript intron_variant - - - - - - rs145609383 X:64158681 G ENSESTG00000023126 ENSESTT00000058492 Transcript intron_variant - - - - - - rs145609383 X:64158681 G 55906 NM_001178033.2 Transcript intron_variant - - - - - - rs145609383 X:64158681 G ENSESTG00000023126 ENSESTT00000058422 Transcript intron_variant - - - - - - rs5918912 X:64226713 G ENSESTG00000023126 ENSESTT00000058394 Transcript intron_variant - - - - - - rs5918912 X:64226713 G 55906 NM_001243804.1 Transcript intron_variant - - - - - - rs5918912 X:64226713 G 55906 NM_001178032.2 Transcript intron_variant - - - - - - rs5918912 X:64226713 G ENSESTG00000023126 ENSESTT00000058422 Transcript intron_variant - - - - - - rs5918916 X:64255430 G ENSESTG00000023126 ENSESTT00000058394 Transcript upstream_gene_variant - - - - - - DISTANCE=816 rs5918916 X:64255430 G 55906 NM_001243804.1 Transcript upstream_gene_variant - - - - - - DISTANCE=806 rs5918916 X:64255430 G 55906 NM_001178032.2 Transcript upstream_gene_variant - - - - - - DISTANCE=806 rs5918916 X:64255430 G ENSESTG00000023126 ENSESTT00000058422 Transcript upstream_gene_variant - - - - - - DISTANCE=816 rs5964409 X:64266910 G - - - intergenic_variant - - - - - - rs5918917 X:64267646 G - - - intergenic_variant - - - - - - rs5918927 X:64347188 G - - - intergenic_variant - - - - - - rs4827359 X:64353968 G - - - intergenic_variant - - - - - - rs5918929 X:64365594 A - - - intergenic_variant - - - - - - rs5918938 X:64536543 G - - - intergenic_variant - - - - - - rs5964966 X:64623764 A - - - intergenic_variant - - - - - - rs4581191 X:64669797 G - - - intergenic_variant - - - - - - rs4827440 X:64708282 G ENSESTG00000010543 ENSESTT00000026378 Transcript upstream_gene_variant - - - - - - DISTANCE=752 rs4827440 X:64708282 G CCDS48131.2 CCDS48131.2 Transcript upstream_gene_variant - - - - - - DISTANCE=400 rs4827440 X:64708282 G 340554 NM_001010888.3 Transcript upstream_gene_variant - - - - - - DISTANCE=333 rs959216 X:64827426 C ENSESTG00000010553 ENSESTT00000026446 Transcript intron_variant - - - - - - rs4827360 X:65102831 C - - - intergenic_variant - - - - - - rs5918591 X:65393658 G 9843 NM_014799.2 Transcript intron_variant - - - - - - rs5918591 X:65393658 G 9843 NM_138737.3 Transcript intron_variant - - - - - - rs5918591 X:65393658 G CCDS48133.1 CCDS48133.1 Transcript intron_variant - - - - - - rs5918591 X:65393658 G ENSESTG00000010608 ENSESTT00000026567 Transcript intron_variant - - - - - - rs5918591 X:65393658 G CCDS14384.3 CCDS14384.3 Transcript intron_variant - - - - - - rs5918591 X:65393658 G ENSESTG00000010608 ENSESTT00000026570 Transcript intron_variant - - - - - - rs5918591 X:65393658 G 9843 NM_001130860.2 Transcript intron_variant - - - - - - rs5918591 X:65393658 G ENSESTG00000010608 ENSESTT00000026559 Transcript intron_variant - - - - - - rs1264213 X:65424235 G 9843 NM_014799.2 Transcript intron_variant - - - - - - rs1264213 X:65424235 G ENSESTG00000010625 ENSESTT00000026591 Transcript downstream_gene_variant - - - - - - DISTANCE=894 rs1264213 X:65424235 G ENSESTG00000010625 ENSESTT00000026597 Transcript intron_variant - - - - - - rs1264213 X:65424235 G CCDS14385.1 CCDS14385.1 Transcript intron_variant - - - - - - rs1264213 X:65424235 G 9843 NM_138737.3 Transcript intron_variant - - - - - - rs1264213 X:65424235 G ENSESTG00000010625 ENSESTT00000026615 Transcript upstream_gene_variant - - - - - - DISTANCE=3783 rs1264213 X:65424235 G CCDS48133.1 CCDS48133.1 Transcript intron_variant - - - - - - rs1264213 X:65424235 G CCDS14384.3 CCDS14384.3 Transcript intron_variant - - - - - - rs1264213 X:65424235 G 9843 NM_001130860.2 Transcript intron_variant - - - - - - rs679562 X:65596486 C - - - intergenic_variant - - - - - - rs616659 X:65602052 G - - - intergenic_variant - - - - - - rs4338248 X:65703421 C - - - intergenic_variant - - - - - - rs6418396 X:65730275 A - - - intergenic_variant - - - - - - rs2336174 X:66537963 C - - - intergenic_variant - - - - - - rs5918751 X:66697679 G - - - intergenic_variant - - - - - - rs10482152 X:67090195 C - - - intergenic_variant - - - - - - rs5918820 X:67405926 G CCDS14388.1 CCDS14388.1 Transcript intron_variant - - - - - - rs5918820 X:67405926 G 4983 NM_002547.2 Transcript intron_variant - - - - - - rs1191948 X:67412906 A ENSESTG00000015048 ENSESTT00000037752 Transcript intron_variant - - - - - - rs1191948 X:67412906 A ENSESTG00000015048 ENSESTT00000037758 Transcript downstream_gene_variant - - - - - - DISTANCE=823 rs1191948 X:67412906 A CCDS14388.1 CCDS14388.1 Transcript intron_variant - - - - - - rs1191948 X:67412906 A 4983 NM_002547.2 Transcript intron_variant - - - - - - rs5965594 X:67692543 T - - - intergenic_variant - - - - - - rs4827419 X:67771421 T - - - intergenic_variant - - - - - - rs792955 X:67980434 C - - - intergenic_variant - - - - - - rs1777639 X:68230998 T - - - intergenic_variant - - - - - - rs5937184 X:68442080 G - ENSR00000479367 RegulatoryFeature regulatory_region_variant - - - - - - rs5937184 X:68442080 G - - - intergenic_variant - - - - - - rs2490725 X:68909685 T CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs2490725 X:68909685 T CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs2490725 X:68909685 T 1896 NM_001005610.2 Transcript intron_variant - - - - - - rs2490725 X:68909685 T CCDS35318.2 CCDS35318.2 Transcript intron_variant - - - - - - rs2490725 X:68909685 T 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs2490725 X:68909685 T 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs2490725 X:68909685 T 1896 NM_001399.4 Transcript intron_variant - - - - - - rs2490725 X:68909685 T 1896 NM_001005613.2 Transcript intron_variant - - - - - - rs2490725 X:68909685 T CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs2188456 X:68958086 T CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs2188456 X:68958086 T CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs2188456 X:68958086 T 1896 NM_001005610.2 Transcript intron_variant - - - - - - rs2188456 X:68958086 T CCDS35318.2 CCDS35318.2 Transcript intron_variant - - - - - - rs2188456 X:68958086 T 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs2188456 X:68958086 T 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs2188456 X:68958086 T 1896 NM_001399.4 Transcript intron_variant - - - - - - rs2188456 X:68958086 T 1896 NM_001005613.2 Transcript intron_variant - - - - - - rs2188456 X:68958086 T CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs2804390 X:68983037 A CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs2804390 X:68983037 A CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs2804390 X:68983037 A 1896 NM_001005610.2 Transcript intron_variant - - - - - - rs2804390 X:68983037 A CCDS35318.2 CCDS35318.2 Transcript intron_variant - - - - - - rs2804390 X:68983037 A 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs2804390 X:68983037 A 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs2804390 X:68983037 A 1896 NM_001399.4 Transcript intron_variant - - - - - - rs2804390 X:68983037 A 1896 NM_001005613.2 Transcript intron_variant - - - - - - rs2804390 X:68983037 A CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs2804350 X:68999793 A CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs2804350 X:68999793 A CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs2804350 X:68999793 A 1896 NM_001005610.2 Transcript intron_variant - - - - - - rs2804350 X:68999793 A CCDS35318.2 CCDS35318.2 Transcript intron_variant - - - - - - rs2804350 X:68999793 A 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs2804350 X:68999793 A 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs2804350 X:68999793 A 1896 NM_001399.4 Transcript intron_variant - - - - - - rs2804350 X:68999793 A 1896 NM_001005613.2 Transcript intron_variant - - - - - - rs2804350 X:68999793 A CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs2520384 X:69000097 T CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs2520384 X:69000097 T CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs2520384 X:69000097 T 1896 NM_001005610.2 Transcript intron_variant - - - - - - rs2520384 X:69000097 T CCDS35318.2 CCDS35318.2 Transcript intron_variant - - - - - - rs2520384 X:69000097 T 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs2520384 X:69000097 T 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs2520384 X:69000097 T 1896 NM_001399.4 Transcript intron_variant - - - - - - rs2520384 X:69000097 T 1896 NM_001005613.2 Transcript intron_variant - - - - - - rs2520384 X:69000097 T CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs2804345 X:69013561 C CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs2804345 X:69013561 C CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs2804345 X:69013561 C 1896 NM_001005610.2 Transcript intron_variant - - - - - - rs2804345 X:69013561 C CCDS35318.2 CCDS35318.2 Transcript intron_variant - - - - - - rs2804345 X:69013561 C 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs2804345 X:69013561 C 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs2804345 X:69013561 C 1896 NM_001399.4 Transcript intron_variant - - - - - - rs2804345 X:69013561 C 1896 NM_001005613.2 Transcript intron_variant - - - - - - rs2804345 X:69013561 C CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs1202988 X:69072622 G CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs1202988 X:69072622 G CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs1202988 X:69072622 G 1896 NM_001005610.2 Transcript intron_variant - - - - - - rs1202988 X:69072622 G CCDS35318.2 CCDS35318.2 Transcript intron_variant - - - - - - rs1202988 X:69072622 G 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs1202988 X:69072622 G 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs1202988 X:69072622 G 1896 NM_001399.4 Transcript intron_variant - - - - - - rs1202988 X:69072622 G 1896 NM_001005613.2 Transcript intron_variant - - - - - - rs1202988 X:69072622 G CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs1203003 X:69080840 A CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs1203003 X:69080840 A CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs1203003 X:69080840 A 1896 NM_001005610.2 Transcript 3_prime_UTR_variant 791 - - - - - rs1203003 X:69080840 A CCDS35318.2 CCDS35318.2 Transcript downstream_gene_variant - - - - - - DISTANCE=141 rs1203003 X:69080840 A 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs1203003 X:69080840 A 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs1203003 X:69080840 A 1896 NM_001399.4 Transcript intron_variant - - - - - - rs1203003 X:69080840 A 1896 NM_001005613.2 Transcript 3_prime_UTR_variant 875 - - - - - rs1203003 X:69080840 A CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs1202963 X:69119304 A 1896 NM_001399.4 Transcript intron_variant - - - - - - rs1202963 X:69119304 A 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs1202963 X:69119304 A CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs1202963 X:69119304 A CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs1202963 X:69119304 A CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs1202963 X:69119304 A 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs1202972 X:69144221 A 1896 NM_001399.4 Transcript intron_variant - - - - - - rs1202972 X:69144221 A 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs1202972 X:69144221 A CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs1202972 X:69144221 A CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs1202972 X:69144221 A CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs1202972 X:69144221 A 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs1202994 X:69148505 T 1896 NM_001399.4 Transcript intron_variant - - - - - - rs1202994 X:69148505 T 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs1202994 X:69148505 T CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs1202994 X:69148505 T CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs1202994 X:69148505 T CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs1202994 X:69148505 T 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs978446 X:69148752 A 1896 NM_001399.4 Transcript intron_variant - - - - - - rs978446 X:69148752 A 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs978446 X:69148752 A CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs978446 X:69148752 A CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs978446 X:69148752 A CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs978446 X:69148752 A 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs1202993 X:69148827 A 1896 NM_001399.4 Transcript intron_variant - - - - - - rs1202993 X:69148827 A 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs1202993 X:69148827 A CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs1202993 X:69148827 A CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs1202993 X:69148827 A CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs1202993 X:69148827 A 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs1576057 X:69198804 G 1896 NM_001399.4 Transcript intron_variant - - - - - - rs1576057 X:69198804 G 1896 NM_001005612.2 Transcript intron_variant - - - - - - rs1576057 X:69198804 G CCDS35319.2 CCDS35319.2 Transcript intron_variant - - - - - - rs1576057 X:69198804 G CCDS43966.1 CCDS43966.1 Transcript intron_variant - - - - - - rs1576057 X:69198804 G CCDS14394.1 CCDS14394.1 Transcript intron_variant - - - - - - rs1576057 X:69198804 G 1896 NM_001005609.1 Transcript intron_variant - - - - - - rs2460035 X:69415569 C ENSESTG00000026313 ENSESTT00000066347 Transcript intron_variant - - - - - - rs2460035 X:69415569 C 347516 NM_198512.1 Transcript intron_variant - - - - - - rs2460035 X:69415569 C CCDS14397.1 CCDS14397.1 Transcript intron_variant - - - - - - rs946451 X:69486614 G CCDS14399.1 CCDS14399.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2622 rs946451 X:69486614 G ENSESTG00000026371 ENSESTT00000066673 Transcript upstream_gene_variant - - - - - - DISTANCE=1581 rs946451 X:69486614 G 407 NM_004312.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1571 rs12556687 X:69662892 T 1741 NM_021120.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1813 rs12556687 X:69662892 T CCDS14403.1 CCDS14403.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2160 rs4844236 X:69744853 G ENSESTG00000020042 ENSESTT00000050307 Transcript downstream_gene_variant - - - - - - DISTANCE=3956 rs4844236 X:69744853 G CCDS43968.1 CCDS43968.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4092 rs4844236 X:69744853 G 56159 NM_031276.2 Transcript downstream_gene_variant - - - - - - DISTANCE=3937 rs4844236 X:69744853 G ENSESTG00000020042 ENSESTT00000050293 Transcript downstream_gene_variant - - - - - - DISTANCE=3938 rs4844236 X:69744853 G 56159 NM_001003811.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3937 rs4844236 X:69744853 G CCDS35323.1 CCDS35323.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4092 rs5936906 X:69751854 G ENSESTG00000020042 ENSESTT00000050307 Transcript intron_variant - - - - - - rs5936906 X:69751854 G CCDS43968.1 CCDS43968.1 Transcript intron_variant - - - - - - rs5936906 X:69751854 G 56159 NM_031276.2 Transcript intron_variant - - - - - - rs5936906 X:69751854 G ENSESTG00000020042 ENSESTT00000050293 Transcript intron_variant - - - - - - rs5936906 X:69751854 G 56159 NM_001003811.1 Transcript intron_variant - - - - - - rs5936906 X:69751854 G CCDS35323.1 CCDS35323.1 Transcript intron_variant - - - - - - rs6525415 X:69998075 C CCDS43968.1 CCDS43968.1 Transcript intron_variant - - - - - - rs6525415 X:69998075 C 56159 NM_031276.2 Transcript intron_variant - - - - - - rs6525415 X:69998075 C 56159 NM_001003811.1 Transcript intron_variant - - - - - - rs6525415 X:69998075 C CCDS35323.1 CCDS35323.1 Transcript intron_variant - - - - - - rs5936991 X:70024032 G CCDS43968.1 CCDS43968.1 Transcript intron_variant - - - - - - rs5936991 X:70024032 G 56159 NM_031276.2 Transcript intron_variant - - - - - - rs5936991 X:70024032 G 56159 NM_001003811.1 Transcript intron_variant - - - - - - rs5936991 X:70024032 G CCDS35323.1 CCDS35323.1 Transcript intron_variant - - - - - - rs4892480 X:72199663 G - - - intergenic_variant - - - - - - rs3117672 X:72261698 C - - - intergenic_variant - - - - - - rs3094744 X:72353058 G - - - intergenic_variant - - - - - - rs239897 X:72492129 A - - - intergenic_variant - - - - - - rs2812017 X:72631758 T - - - intergenic_variant - - - - - - rs2733936 X:72635310 T - - - intergenic_variant - - - - - - rs2812020 X:72637999 A - - - intergenic_variant - - - - - - rs5937260 X:73271846 C 100302692 NR_028379.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5937260 X:73271846 C 554203 NR_024582.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5937767 X:73370571 T 100302692 NR_028379.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1313777 X:73397214 A 100302692 NR_028379.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1313776 X:73397993 G 100302692 NR_028379.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs174206 X:73441602 C 100500807 NR_037511.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3149 rs174206 X:73441602 C 100302692 NR_028379.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs174206 X:73441602 C 100126317 NR_030620.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3149 rs174206 X:73441602 C ENSESTG00000017604 ENSESTT00000044290 Transcript intron_variant - - - - - - rs174206 X:73441602 C 693122 NR_030398.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3306 rs478537 X:73675883 T ENSESTG00000017456 ENSESTT00000043944 Transcript intron_variant - - - - - - rs478537 X:73675883 T 6567 NM_006517.4 Transcript intron_variant - - - - - - rs6655611 X:74004946 C 340533 NM_001008537.2 Transcript intron_variant - - - - - - rs2367253 X:74917574 A - - - intergenic_variant - - - - - - rs2202295 X:75145032 G - - - intergenic_variant - - - - - - rs141915241 X:75300262 G - - - intergenic_variant - - - - - - rs975923 X:75554873 C ENSESTG00000035173 ENSESTT00000088878 Transcript downstream_gene_variant - - - - - - DISTANCE=548 rs1298033 X:75891955 C - - - intergenic_variant - - - - - - rs5937600 X:75929648 T - - - intergenic_variant - - - - - - rs6648232 X:76212224 G - - - intergenic_variant - - - - - - rs1894548 X:76967526 A ENSESTG00000027940 ENSESTT00000070401 Transcript intron_variant - - - - - - rs1894548 X:76967526 A 546 NM_138270.2 Transcript intron_variant - - - - - - rs1894548 X:76967526 A 546 NM_000489.3 Transcript intron_variant - - - - - - rs1894548 X:76967526 A ENSESTG00000027940 ENSESTT00000070409 Transcript intron_variant - - - - - - rs1894548 X:76967526 A CCDS14435.1 CCDS14435.1 Transcript intron_variant - - - - - - rs1894548 X:76967526 A CCDS14434.1 CCDS14434.1 Transcript intron_variant - - - - - - rs6524037 X:77095338 C CCDS14436.2 CCDS14436.2 Transcript intron_variant - - - - - - rs6524037 X:77095338 C 84061 NM_032121.5 Transcript intron_variant - - - - - - rs5913631 X:77296047 C 538 NM_000052.5 Transcript intron_variant - - - - - - rs5913631 X:77296047 C ENSESTG00000027738 ENSESTT00000069857 Transcript intron_variant - - - - - - rs5913631 X:77296047 C CCDS35339.1 CCDS35339.1 Transcript intron_variant - - - - - - rs4826245 X:77298857 A 538 NM_000052.5 Transcript missense_variant 4208 4048 1350 E/K Gag/Aag - PolyPhen=benign;SIFT=tolerated rs4826245 X:77298857 A ENSESTG00000027738 ENSESTT00000069857 Transcript downstream_gene_variant - - - - - - DISTANCE=644 rs4826245 X:77298857 A CCDS35339.1 CCDS35339.1 Transcript missense_variant 4048 4048 1350 E/K Gag/Aag - PolyPhen=benign;SIFT=tolerated rs142373151 X:77418672 G - ENSR00000260721 RegulatoryFeature regulatory_region_variant - - - - - - rs142373151 X:77418672 G - - - intergenic_variant - - - - - - rs321084 X:77553647 A 10800 NM_006639.2 Transcript intron_variant - - - - - - rs321084 X:77553647 A ENSESTG00000027837 ENSESTT00000070095 Transcript intron_variant - - - - - - rs5912617 X:77761342 C - - - intergenic_variant - - - - - - rs3123298 X:78023360 C - - - intergenic_variant - - - - - - rs5959192 X:78025974 C - - - intergenic_variant - - - - - - rs5912648 X:78048660 C - - - intergenic_variant - - - - - - rs5912180 X:78062078 G - - - intergenic_variant - - - - - - rs5912665 X:78095520 C - - - intergenic_variant - - - - - - rs5912190 X:78135679 A - - - intergenic_variant - - - - - - rs612005 X:78210341 A ENSESTG00000031208 ENSESTT00000078698 Transcript intron_variant - - - - - - rs612005 X:78210341 A ENSESTG00000031208 ENSESTT00000078735 Transcript intron_variant - - - - - - rs612005 X:78210341 A 27334 NM_198333.1 Transcript intron_variant - - - - - - rs612005 X:78210341 A ENSESTG00000031208 ENSESTT00000078744 Transcript intron_variant - - - - - - rs612005 X:78210341 A 27334 NM_014499.2 Transcript intron_variant - - - - - - rs612005 X:78210341 A ENSESTG00000031208 ENSESTT00000078709 Transcript intron_variant - - - - - - rs4825974 X:78252581 G - - - intergenic_variant - - - - - - rs5912708 X:78271410 G - - - intergenic_variant - - - - - - rs2152774 X:78310225 A - - - intergenic_variant - - - - - - rs5912787 X:78420575 C - - - intergenic_variant - - - - - - rs2411962 X:78499988 G - - - intergenic_variant - - - - - - rs5959342 X:78655917 C - - - intergenic_variant - - - - - - rs6523742 X:79362103 G - - - intergenic_variant - - - - - - rs490504 X:79380502 T - - - intergenic_variant - - - - - - rs619752 X:79380597 T - - - intergenic_variant - - - - - - rs454979 X:79419500 A - - - intergenic_variant - - - - - - rs194957 X:79435011 A - - - intergenic_variant - - - - - - rs371265 X:79452975 T - - - intergenic_variant - - - - - - rs428952 X:79458206 T - - - intergenic_variant - - - - - - rs1548021 X:79537608 T - - - intergenic_variant - - - - - - rs5913352 X:80201783 C - - - intergenic_variant - - - - - - rs5913412 X:80479762 A 6451 NM_003022.2 Transcript intron_variant - - - - - - rs5913412 X:80479762 A CCDS14449.1 CCDS14449.1 Transcript intron_variant - - - - - - rs5913412 X:80479762 A ENSESTG00000024556 ENSESTT00000062093 Transcript intron_variant - - - - - - rs5959934 X:80871418 A - - - intergenic_variant - - - - - - rs982349 X:81106779 A - - - intergenic_variant - - - - - - rs2516133 X:81134434 T - - - intergenic_variant - - - - - - rs5922825 X:81201055 A - - - intergenic_variant - - - - - - rs1794604 X:81237324 C - ENSR00000260761 RegulatoryFeature regulatory_region_variant - - - - - - rs1794604 X:81237324 C - - - intergenic_variant - - - - - - rs1536458 X:81341893 G - - - intergenic_variant - - - - - - rs5967869 X:81619697 C - - - intergenic_variant - - - - - - rs5924518 X:81810096 G - - - intergenic_variant - - - - - - rs2142868 X:81944924 A - - - intergenic_variant - - - - - - rs5922638 X:82030816 A - - - intergenic_variant - - - - - - rs5922747 X:82247860 G - - - intergenic_variant - - - - - - rs4828213 X:82280338 A - - - intergenic_variant - - - - - - rs2205955 X:82298369 A - - - intergenic_variant - - - - - - rs4828221 X:82330751 G - - - intergenic_variant - - - - - - rs2213427 X:82773783 C - - - intergenic_variant - - - - - - rs5921990 X:82920454 T - - - intergenic_variant - - - - - - rs4564031 X:83015005 A - ENSR00000660824 RegulatoryFeature regulatory_region_variant - - - - - - rs4564031 X:83015005 A - - - intergenic_variant - - - - - - rs4620436 X:83167671 C - - - intergenic_variant - - - - - - rs5922917 X:83420757 A ENSESTG00000033479 ENSESTT00000084638 Transcript intron_variant - - - - - - rs5922917 X:83420757 A CCDS14451.1 CCDS14451.1 Transcript intron_variant - - - - - - rs5922917 X:83420757 A 27330 NM_014496.4 Transcript intron_variant - - - - - - rs5922054 X:83734459 T 139324 NM_144657.4 Transcript intron_variant - - - - - - rs5922054 X:83734459 T ENSESTG00000027316 ENSESTT00000069024 Transcript upstream_gene_variant - - - - - - DISTANCE=4046 rs5922054 X:83734459 T CCDS35342.1 CCDS35342.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4054 rs5922054 X:83734459 T ENSESTG00000033471 ENSESTT00000084588 Transcript intron_variant - - - - - - rs5922054 X:83734459 T 139324 NM_001177479.1 Transcript intron_variant - - - - - - rs5922054 X:83734459 T ENSESTG00000027316 ENSESTT00000068955 Transcript intron_variant - - - - - - rs5922054 X:83734459 T 139324 NM_001177478.1 Transcript intron_variant - - - - - - rs5922054 X:83734459 T ENSESTG00000027316 ENSESTT00000068800 Transcript intron_variant - - - - - - rs5968350 X:83800445 G - - - intergenic_variant - - - - - - rs4828278 X:83823823 C - - - intergenic_variant - - - - - - rs4593712 X:83981019 G - - - intergenic_variant - - - - - - rs5923096 X:84001928 T - - - intergenic_variant - - - - - - rs5922099 X:84070907 G - - - intergenic_variant - - - - - - rs608096 X:84188735 A ENSESTG00000027017 ENSESTT00000068080 Transcript upstream_gene_variant - - - - - - DISTANCE=531 rs608096 X:84188735 A 100131816 NR_024062.1 Transcript upstream_gene_variant - - - - - - DISTANCE=422 rs473284 X:84219734 G - - - intergenic_variant - - - - - - rs644973 X:84227229 T - - - intergenic_variant - - - - - - rs574059 X:84230231 C - - - intergenic_variant - - - - - - rs2032573 X:84409749 G ENSESTG00000027296 ENSESTT00000068738 Transcript intron_variant - - - - - - rs2032573 X:84409749 G ENSESTG00000027285 ENSESTT00000068732 Transcript intron_variant - - - - - - rs4828336 X:84490304 C ENSESTG00000027285 ENSESTT00000068732 Transcript intron_variant - - - - - - rs5968474 X:84572836 C ENSESTG00000027192 ENSESTT00000068709 Transcript intron_variant - - - - - - rs5968474 X:84572836 C 79983 NM_024921.3 Transcript intron_variant - - - - - - rs5968474 X:84572836 C CCDS14452.1 CCDS14452.1 Transcript intron_variant - - - - - - rs5967558 X:84733300 T - - - intergenic_variant - - - - - - rs5923322 X:84744579 G - - - intergenic_variant - - - - - - rs4240066 X:84866536 C - - - intergenic_variant - - - - - - rs4639657 X:84947874 G - - - intergenic_variant - - - - - - rs3116781 X:84979955 T - - - intergenic_variant - - - - - - rs1883312 X:85074617 C - - - intergenic_variant - - - - - - rs1115522 X:85201073 T CCDS14454.1 CCDS14454.1 Transcript intron_variant - - - - - - rs1115522 X:85201073 T 1121 NM_000390.2 Transcript intron_variant - - - - - - rs2665789 X:85399162 G CCDS48140.1 CCDS48140.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4463 rs2665789 X:85399162 G 117154 NM_001139514.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4293 rs2665789 X:85399162 G 117154 NM_053281.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4293 rs2665789 X:85399162 G CCDS14455.1 CCDS14455.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4463 rs6623690 X:85784527 G CCDS48140.1 CCDS48140.1 Transcript intron_variant - - - - - - rs6623690 X:85784527 G 117154 NM_001139514.1 Transcript intron_variant - - - - - - rs6623690 X:85784527 G CCDS55457.1 CCDS55457.1 Transcript intron_variant - - - - - - rs6623690 X:85784527 G 117154 NM_053281.3 Transcript intron_variant - - - - - - rs6623690 X:85784527 G CCDS14455.1 CCDS14455.1 Transcript intron_variant - - - - - - rs6623690 X:85784527 G 117154 NM_001139515.1 Transcript intron_variant - - - - - - rs5922266 X:85897939 C CCDS48140.1 CCDS48140.1 Transcript intron_variant - - - - - - rs5922266 X:85897939 C 117154 NM_001139514.1 Transcript intron_variant - - - - - - rs5922266 X:85897939 C CCDS55457.1 CCDS55457.1 Transcript intron_variant - - - - - - rs5922266 X:85897939 C 117154 NM_053281.3 Transcript intron_variant - - - - - - rs5922266 X:85897939 C CCDS14455.1 CCDS14455.1 Transcript intron_variant - - - - - - rs5922266 X:85897939 C 117154 NM_001139515.1 Transcript intron_variant - - - - - - rs1539557 X:85999348 T ENSESTG00000016561 ENSESTT00000041540 Transcript intron_variant - - - - - - rs1539557 X:85999348 T 117154 NM_001139514.1 Transcript intron_variant - - - - - - rs1539557 X:85999348 T 117154 NM_053281.3 Transcript intron_variant - - - - - - rs1539557 X:85999348 T CCDS14455.1 CCDS14455.1 Transcript intron_variant - - - - - - rs1539557 X:85999348 T CCDS48140.1 CCDS48140.1 Transcript intron_variant - - - - - - rs1539557 X:85999348 T ENSESTG00000016561 ENSESTT00000041559 Transcript intron_variant - - - - - - rs1539557 X:85999348 T CCDS55457.1 CCDS55457.1 Transcript intron_variant - - - - - - rs1539557 X:85999348 T 117154 NM_001139515.1 Transcript intron_variant - - - - - - rs5922287 X:86013646 A ENSESTG00000016561 ENSESTT00000041540 Transcript intron_variant - - - - - - rs5922287 X:86013646 A 117154 NM_001139514.1 Transcript intron_variant - - - - - - rs5922287 X:86013646 A 117154 NM_053281.3 Transcript intron_variant - - - - - - rs5922287 X:86013646 A CCDS14455.1 CCDS14455.1 Transcript intron_variant - - - - - - rs5922287 X:86013646 A CCDS48140.1 CCDS48140.1 Transcript intron_variant - - - - - - rs5922287 X:86013646 A ENSESTG00000016561 ENSESTT00000041559 Transcript intron_variant - - - - - - rs5922287 X:86013646 A CCDS55457.1 CCDS55457.1 Transcript intron_variant - - - - - - rs5922287 X:86013646 A 117154 NM_001139515.1 Transcript intron_variant - - - - - - rs1291748 X:86153195 C - - - intergenic_variant - - - - - - rs2710051 X:86186131 T - - - intergenic_variant - - - - - - rs5923802 X:86366418 G - - - intergenic_variant - - - - - - rs5922410 X:86507697 C - - - intergenic_variant - - - - - - rs604432 X:86607833 C - - - intergenic_variant - - - - - - rs726747 X:87031937 A ENSESTG00000006203 ENSESTT00000015599 Transcript intron_variant - - - - - - rs6617502 X:87472165 A - - - intergenic_variant - - - - - - rs4893349 X:87807591 G - - - intergenic_variant - - - - - - rs5941442 X:87914272 T - - - intergenic_variant - - - - - - rs981717 X:87937493 T - - - intergenic_variant - - - - - - rs6617773 X:88147094 T - - - intergenic_variant - - - - - - rs5942323 X:88185926 A - - - intergenic_variant - - - - - - rs5941113 X:88199878 G - - - intergenic_variant - - - - - - rs4279765 X:88326255 A - ENSR00000480134 RegulatoryFeature regulatory_region_variant - - - - - - rs4279765 X:88326255 A - - - intergenic_variant - - - - - - rs964878 X:88355792 C - - - intergenic_variant - - - - - - rs5942388 X:88359605 C - - - intergenic_variant - - - - - - rs5942390 X:88360895 C - - - intergenic_variant - - - - - - rs4408071 X:88382928 G - - - intergenic_variant - - - - - - rs150918308 X:88400977 C - - - intergenic_variant - - - - - - rs5940883 X:90144495 C - - - intergenic_variant - - - - - - rs2896810 X:90355719 T - - - intergenic_variant - - - - - - rs4893326 X:91916030 C - - - intergenic_variant - - - - - - rs4893331 X:91969517 A - - - intergenic_variant - - - - - - rs785750 X:92416892 T - - - intergenic_variant - - - - - - rs2206052 X:92632567 T - - - intergenic_variant - - - - - - rs5940191 X:92690331 G - - - intergenic_variant - - - - - - rs1206197 X:92705248 T - - - intergenic_variant - - - - - - rs2205700 X:92906577 A - - - intergenic_variant - - - - - - rs1014475 X:93005512 A - - - intergenic_variant - - - - - - rs5939544 X:93205322 G - - - intergenic_variant - - - - - - rs1578603 X:93262061 G - - - intergenic_variant - - - - - - rs2799921 X:93582328 G - - - intergenic_variant - - - - - - rs2903906 X:94190334 G - - - intergenic_variant - - - - - - rs6522857 X:94196706 G - - - intergenic_variant - - - - - - rs5950222 X:94417572 A - - - intergenic_variant - - - - - - rs3122216 X:94553213 T - - - intergenic_variant - - - - - - rs3131397 X:94556586 A - - - intergenic_variant - - - - - - rs5949556 X:94567921 A - - - intergenic_variant - - - - - - rs76728322 X:94643586 T - - - intergenic_variant - - - - - - rs2142777 X:94721069 T - - - intergenic_variant - - - - - - rs5990325 X:94723211 T - - - intergenic_variant - - - - - - rs5990110 X:94765865 A - - - intergenic_variant - - - - - - rs5949298 X:94792169 T - - - intergenic_variant - - - - - - rs1578755 X:94853646 C - - - intergenic_variant - - - - - - rs4969565 X:94929744 A ENSESTG00000014131 ENSESTT00000035325 Transcript downstream_gene_variant - - - - - - DISTANCE=4354 rs4560977 X:94964626 C - - - intergenic_variant - - - - - - rs1926109 X:95017462 G - - - intergenic_variant - - - - - - rs1926117 X:95096596 C - - - intergenic_variant - - - - - - rs5949705 X:95175266 T - - - intergenic_variant - - - - - - rs2147052 X:95212397 C - - - intergenic_variant - - - - - - rs2743679 X:95335413 C - - - intergenic_variant - - - - - - rs1018380 X:95349446 T - - - intergenic_variant - - - - - - rs1150272 X:95514128 T - - - intergenic_variant - - - - - - rs4492548 X:95958630 T CCDS14468.1 CCDS14468.1 Transcript intron_variant - - - - - - rs4492548 X:95958630 T 1730 NM_007309.3 Transcript intron_variant - - - - - - rs4492548 X:95958630 T CCDS14467.1 CCDS14467.1 Transcript intron_variant - - - - - - rs4492548 X:95958630 T ENSESTG00000024069 ENSESTT00000060863 Transcript intron_variant - - - - - - rs4492548 X:95958630 T 1730 NM_006729.4 Transcript intron_variant - - - - - - rs4492548 X:95958630 T ENSESTG00000024069 ENSESTT00000060909 Transcript intron_variant - - - - - - rs28580757 X:96083935 A CCDS14468.1 CCDS14468.1 Transcript intron_variant - - - - - - rs28580757 X:96083935 A 1730 NM_007309.3 Transcript intron_variant - - - - - - rs28580757 X:96083935 A CCDS14467.1 CCDS14467.1 Transcript intron_variant - - - - - - rs28580757 X:96083935 A 1730 NM_006729.4 Transcript intron_variant - - - - - - rs28580757 X:96083935 A ENSESTG00000024069 ENSESTT00000060922 Transcript intron_variant - - - - - - rs28580757 X:96083935 A ENSESTG00000024069 ENSESTT00000060909 Transcript intron_variant - - - - - - rs853485 X:96141497 T 1730 NM_007309.3 Transcript intron_variant - - - - - - rs853485 X:96141497 T CCDS14467.1 CCDS14467.1 Transcript intron_variant - - - - - - rs853485 X:96141497 T ENSESTG00000024069 ENSESTT00000060956 Transcript intron_variant - - - - - - rs853485 X:96141497 T CCDS35345.1 CCDS35345.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1402 rs853485 X:96141497 T 29935 NM_013347.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1031 rs853485 X:96141497 T CCDS14468.1 CCDS14468.1 Transcript intron_variant - - - - - - rs853485 X:96141497 T 1730 NM_006729.4 Transcript intron_variant - - - - - - rs853485 X:96141497 T ENSESTG00000024069 ENSESTT00000060909 Transcript intron_variant - - - - - - rs853485 X:96141497 T ENSESTG00000024069 ENSESTT00000060922 Transcript downstream_gene_variant - - - - - - DISTANCE=4817 rs1544302 X:96492507 G CCDS14468.1 CCDS14468.1 Transcript intron_variant - - - - - - rs1544302 X:96492507 G 1730 NM_007309.3 Transcript intron_variant - - - - - - rs1544302 X:96492507 G ENSESTG00000024132 ENSESTT00000061183 Transcript intron_variant - - - - - - rs1544302 X:96492507 G CCDS14467.1 CCDS14467.1 Transcript intron_variant - - - - - - rs1544302 X:96492507 G 1730 NM_006729.4 Transcript intron_variant - - - - - - rs318126 X:97203621 A - - - intergenic_variant - - - - - - rs1458776 X:97387960 C - - - intergenic_variant - - - - - - rs1325724 X:97643243 C - - - intergenic_variant - - - - - - rs5921172 X:97905430 G - - - intergenic_variant - - - - - - rs2335830 X:97956449 T - - - intergenic_variant - - - - - - rs5920690 X:97969782 G - - - intergenic_variant - - - - - - rs226721 X:98455412 C - - - intergenic_variant - - - - - - rs226730 X:98509006 A - - - intergenic_variant - - - - - - rs760695 X:98728741 T 442459 NR_024608.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2095964 X:99043676 T 442459 NR_024608.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1221122 X:99076701 T 442459 NR_024608.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1462575 X:99209137 A - - - intergenic_variant - - - - - - rs4827984 X:99268699 A - - - intergenic_variant - - - - - - rs1387280 X:99388122 A - - - intergenic_variant - - - - - - rs5920804 X:99437928 C - - - intergenic_variant - - - - - - rs6523345 X:99504405 T - - - intergenic_variant - - - - - - rs1335263 X:99556677 A ENSESTG00000032585 ENSESTT00000082257 Transcript intron_variant - - - - - - rs1335263 X:99556677 A CCDS43976.1 CCDS43976.1 Transcript intron_variant - - - - - - rs1335263 X:99556677 A 57526 NM_001105243.1 Transcript intron_variant - - - - - - rs1335263 X:99556677 A CCDS55462.1 CCDS55462.1 Transcript intron_variant - - - - - - rs1335263 X:99556677 A 57526 NM_001184880.1 Transcript intron_variant - - - - - - rs1335263 X:99556677 A 57526 NM_020766.2 Transcript intron_variant - - - - - - rs1335263 X:99556677 A CCDS48141.1 CCDS48141.1 Transcript intron_variant - - - - - - rs2359744 X:99850254 C CCDS14469.1 CCDS14469.1 Transcript intron_variant - - - - - - rs2359744 X:99850254 C 64102 NM_022144.2 Transcript intron_variant - - - - - - rs2359744 X:99850254 C ENSESTG00000032121 ENSESTT00000081101 Transcript upstream_gene_variant - - - - - - DISTANCE=3757 rs2359744 X:99850254 C ENSESTG00000032121 ENSESTT00000081095 Transcript intron_variant - - - - - - rs2359744 X:99850254 C ENSESTG00000032121 ENSESTT00000081063 Transcript downstream_gene_variant - - - - - - DISTANCE=963 rs2858182 X:99962121 G 94121 NM_080737.2 Transcript intron_variant - - - - - - rs2858182 X:99962121 G 94121 NM_001129896.2 Transcript intron_variant - - - - - - rs2858182 X:99962121 G 94121 NM_001174068.1 Transcript intron_variant - - - - - - rs2858182 X:99962121 G ENSESTG00000032518 ENSESTT00000082157 Transcript intron_variant - - - - - - rs2858182 X:99962121 G ENSESTG00000032518 ENSESTT00000082158 Transcript intron_variant - - - - - - rs2858182 X:99962121 G ENSESTG00000032518 ENSESTT00000082151 Transcript intron_variant - - - - - - rs4828053 X:99997342 T - - - intergenic_variant - - - - - - rs2154371 X:100017906 C - - - intergenic_variant - - - - - - rs5921685 X:100140904 G - - - intergenic_variant - - - - - - rs5920897 X:100521688 C 1821 NM_001939.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2203 rs5920897 X:100521688 C CCDS55466.1 CCDS55466.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2493 rs5920897 X:100521688 C ENSESTG00000032383 ENSESTT00000081748 Transcript downstream_gene_variant - - - - - - DISTANCE=2299 rs5920897 X:100521688 C CCDS35347.1 CCDS35347.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2493 rs5920897 X:100521688 C 54457 NM_024885.3 Transcript downstream_gene_variant - - - - - - DISTANCE=1553 rs5920897 X:100521688 C 54457 NM_001168474.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1553 rs5920897 X:100521688 C 1821 NM_001171184.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2203 rs6523479 X:100570953 A - - - intergenic_variant - - - - - - rs5951326 X:100710663 T 100131755 NR_028407.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951326 X:100710663 T ENSESTG00000017501 ENSESTT00000044056 Transcript intron_variant - - - - - - rs5951326 X:100710663 T ENSESTG00000017501 ENSESTT00000044017 Transcript intron_variant - - - - - - rs5951265 X:100712309 C 100131755 NR_028407.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951265 X:100712309 C ENSESTG00000017501 ENSESTT00000044056 Transcript intron_variant - - - - - - rs5951265 X:100712309 C ENSESTG00000017501 ENSESTT00000044017 Transcript intron_variant - - - - - - rs5991911 X:100748078 G ENSESTG00000017728 ENSESTT00000044674 Transcript intron_variant - - - - - - rs5991911 X:100748078 G ENSESTG00000017501 ENSESTT00000044105 Transcript downstream_gene_variant - - - - - - DISTANCE=4417 rs5991911 X:100748078 G 100131755 NR_045862.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5991911 X:100748078 G CCDS59170.1 CCDS59170.1 Transcript missense_variant 4502 4502 1501 D/G gAc/gGc - PolyPhen=benign;SIFT=tolerated rs5991911 X:100748078 G 100131755 NR_045864.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5991911 X:100748078 G 100131755 NR_028407.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs5991911 X:100748078 G 100131755 NR_045861.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5991911 X:100748078 G 100131755 NM_001256155.1 Transcript missense_variant 4704 4502 1501 D/G gAc/gGc - PolyPhen=benign;SIFT=tolerated rs5991911 X:100748078 G 100131755 NR_045863.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951337 X:100756917 T 100131755 NR_045861.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951337 X:100756917 T 100131755 NR_028407.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951337 X:100756917 T 100131755 NR_045862.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951337 X:100756917 T 100131755 NR_045864.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951337 X:100756917 T 100131755 NR_045863.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951338 X:100763900 T 100131755 NR_045861.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951338 X:100763900 T 100131755 NR_028407.2 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951338 X:100763900 T 100131755 NR_045862.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951338 X:100763900 T 100131755 NR_045864.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951338 X:100763900 T 100131755 NR_045863.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs7877615 X:100914185 C - ENSR00001031029 RegulatoryFeature regulatory_region_variant - - - - - - rs7877615 X:100914185 C CCDS14490.1 CCDS14490.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1611 rs7877615 X:100914185 C ENSESTG00000017695 ENSESTT00000044585 Transcript upstream_gene_variant - - - - - - DISTANCE=3218 rs7877615 X:100914185 C 9823 NM_177949.2 Transcript intron_variant - - - - - - rs7877615 X:100914185 C ENSESTG00000017648 ENSESTT00000044520 Transcript intron_variant - - - - - - rs7877615 X:100914185 C 9823 NM_014782.5 Transcript intron_variant - - - - - - rs7877615 X:100914185 C ENSESTG00000017648 ENSESTT00000044533 Transcript intron_variant - - - - - - rs7877615 X:100914185 C ENSESTG00000017648 ENSESTT00000044559 Transcript intron_variant - - - - - - rs7877615 X:100914185 C ENSESTG00000017648 ENSESTT00000044546 Transcript intron_variant - - - - - - rs7877615 X:100914185 C ENSESTG00000017648 ENSESTT00000044500 Transcript intron_variant - - - - - - rs7054871 X:101011478 T - - - intergenic_variant - - - - - - rs5944882 X:101138792 C ENSESTG00000017634 ENSESTT00000044447 Transcript downstream_gene_variant - - - - - - DISTANCE=477 rs5944882 X:101138792 C 84460 NR_046009.1 Transcript non_coding_exon_variant,nc_transcript_variant 2460 - - - - - rs5944882 X:101138792 C 84460 NR_046008.1 Transcript non_coding_exon_variant,nc_transcript_variant 2513 - - - - - rs5944882 X:101138792 C CCDS35348.1 CCDS35348.1 Transcript missense_variant 1607 1607 536 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs5944882 X:101138792 C 84460 NM_001011657.3 Transcript missense_variant 1957 1607 536 Q/R cAg/cGg - PolyPhen=benign;SIFT=tolerated rs4599977 X:101355940 A - - - intergenic_variant - - - - - - rs5945038 X:101405696 A 340542 NM_001012978.2 Transcript downstream_gene_variant - - - - - - DISTANCE=2983 rs5945038 X:101405696 A 340542 NM_001159560.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2983 rs5945038 X:101405696 A CCDS35350.1 CCDS35350.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3206 rs5986806 X:101407150 C 340542 NM_001012978.2 Transcript downstream_gene_variant - - - - - - DISTANCE=1529 rs5986806 X:101407150 C 340542 NM_001159560.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1529 rs5986806 X:101407150 C CCDS35350.1 CCDS35350.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1752 rs4907865 X:102241158 A - - - intergenic_variant - - - - - - rs4907873 X:102379083 C - - - intergenic_variant - - - - - - rs5945952 X:102482350 T - - - intergenic_variant - - - - - - rs5945957 X:102497300 C - - - intergenic_variant - - - - - - rs5945970 X:102577755 G - - - intergenic_variant - - - - - - rs2858074 X:102739478 A - - - intergenic_variant - - - - - - rs1180890 X:102744483 T - - - intergenic_variant - - - - - - rs533946 X:103001342 T ENSESTG00000017355 ENSESTT00000043666 Transcript intron_variant - - - - - - rs533946 X:103001342 T ENSESTG00000017355 ENSESTT00000043654 Transcript intron_variant - - - - - - rs544931 X:103089408 C 51209 NM_016370.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2196 rs1013752 X:103301148 T 286436 NM_001164416.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4127 rs178106 X:103330913 C - - - intergenic_variant - - - - - - rs2051586 X:103358090 C - ENSR00001031036 RegulatoryFeature regulatory_region_variant - - - - - - rs2051586 X:103358090 C 644353 NM_001143978.1 Transcript intron_variant - - - - - - rs2051586 X:103358090 C 644353 NR_026694.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs2051586 X:103358090 C 401612 NM_001012755.3 Transcript intron_variant - - - - - - rs4549907 X:103364693 T 644353 NM_001143978.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4160 rs4549907 X:103364693 T 286437 NR_039980.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2297 rs4549907 X:103364693 T 644353 NR_026694.1 Transcript downstream_gene_variant - - - - - - DISTANCE=4160 rs4549907 X:103364693 T 401612 NM_001012755.3 Transcript intron_variant - - - - - - rs2142687 X:103981422 C CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs2142687 X:103981422 C 26280 NM_017416.1 Transcript intron_variant - - - - - - rs2187709 X:104025890 A CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs2187709 X:104025890 A 26280 NM_017416.1 Transcript intron_variant - - - - - - rs2213339 X:104028594 G CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs2213339 X:104028594 G 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5962457 X:104300339 A CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5962457 X:104300339 A 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5916728 X:104423975 T CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5916728 X:104423975 T 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5916882 X:104425905 A CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5916882 X:104425905 A 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5962478 X:104477752 G CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5962478 X:104477752 G 26280 NM_017416.1 Transcript intron_variant - - - - - - rs2392689 X:104500518 C CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs2392689 X:104500518 C 26280 NM_017416.1 Transcript intron_variant - - - - - - rs222598 X:104603000 C CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs222598 X:104603000 C 26280 NM_017416.1 Transcript intron_variant - - - - - - rs222600 X:104604320 G CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs222600 X:104604320 G 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5916913 X:104709733 G CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5916913 X:104709733 G 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5916734 X:104721569 T - ENSR00001490865 RegulatoryFeature regulatory_region_variant - - - - - - rs5916734 X:104721569 T CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5916734 X:104721569 T 26280 NM_017416.1 Transcript intron_variant - - - - - - rs1012024 X:104723258 T CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs1012024 X:104723258 T 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5916915 X:104724209 T CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5916915 X:104724209 T 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5916916 X:104751534 G CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5916916 X:104751534 G 26280 NM_017416.1 Transcript intron_variant - - - - - - rs210727 X:104827041 T CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs210727 X:104827041 T 26280 NM_017416.1 Transcript intron_variant - - - - - - rs210557 X:104908816 A CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs210557 X:104908816 A 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5916949 X:104981457 G CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5916949 X:104981457 G 26280 NM_017416.1 Transcript intron_variant - - - - - - rs5916951 X:104988630 T CCDS14517.1 CCDS14517.1 Transcript intron_variant - - - - - - rs5916951 X:104988630 T 26280 NM_017416.1 Transcript intron_variant - - - - - - rs4826891 X:105062716 A ENSESTG00000035599 ENSESTT00000089911 Transcript upstream_gene_variant - - - - - - DISTANCE=3843 rs4826891 X:105062716 A 203447 NM_198465.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3820 rs393929 X:105092456 A ENSESTG00000035599 ENSESTT00000089911 Transcript intron_variant - - - - - - rs393929 X:105092456 A 203447 NM_198465.2 Transcript intron_variant - - - - - - rs209372 X:105153001 G ENSESTG00000035599 ENSESTT00000089912 Transcript synonymous_variant 1246 1203 401 K aaA/aaG - rs209372 X:105153001 G 203447 NM_198465.2 Transcript synonymous_variant 1671 1368 456 K aaA/aaG - rs447326 X:105344752 G - - - intergenic_variant - - - - - - rs381252 X:105352750 G - - - intergenic_variant - - - - - - rs2392851 X:105365028 T - - - intergenic_variant - - - - - - rs373601 X:105366069 T - - - intergenic_variant - - - - - - rs4826892 X:105429445 C ENSESTG00000035603 ENSESTT00000089930 Transcript intron_variant - - - - - - rs4826892 X:105429445 C 139221 NM_152423.4 Transcript intron_variant - - - - - - rs4826892 X:105429445 C 139221 NM_001171020.1 Transcript intron_variant - - - - - - rs4826892 X:105429445 C ENSESTG00000035603 ENSESTT00000089920 Transcript intron_variant - - - - - - rs4826892 X:105429445 C ENSESTG00000035603 ENSESTT00000089919 Transcript intron_variant - - - - - - rs2754829 X:105468084 A - - - intergenic_variant - - - - - - rs418143 X:105526816 C - - - intergenic_variant - - - - - - rs5916983 X:105597425 G - - - intergenic_variant - - - - - - rs5962333 X:105602761 A - - - intergenic_variant - - - - - - rs5916994 X:105668555 T - - - intergenic_variant - - - - - - rs5916760 X:105759772 G - - - intergenic_variant - - - - - - rs4826960 X:106566605 C - - - intergenic_variant - - - - - - rs4342758 X:106979336 A ENSESTG00000018333 ENSESTT00000046154 Transcript intron_variant - - - - - - rs4342758 X:106979336 A ENSESTG00000018333 ENSESTT00000046187 Transcript intron_variant - - - - - - rs4342758 X:106979336 A ENSESTG00000018333 ENSESTT00000046209 Transcript intron_variant - - - - - - rs4342758 X:106979336 A ENSESTG00000018333 ENSESTT00000046239 Transcript intron_variant - - - - - - rs4342758 X:106979336 A 1831 NM_198057.2 Transcript intron_variant - - - - - - rs4342758 X:106979336 A ENSESTG00000018333 ENSESTT00000046224 Transcript intron_variant - - - - - - rs4342758 X:106979336 A CCDS14530.1 CCDS14530.1 Transcript intron_variant - - - - - - rs4342758 X:106979336 A ENSESTG00000018333 ENSESTT00000046172 Transcript intron_variant - - - - - - rs4342758 X:106979336 A ENSESTG00000018333 ENSESTT00000046218 Transcript intron_variant - - - - - - rs5962899 X:107090543 A CCDS14532.2 CCDS14532.2 Transcript intron_variant - - - - - - rs5962899 X:107090543 A CCDS14533.2 CCDS14533.2 Transcript intron_variant - - - - - - rs5962899 X:107090543 A 11043 NM_012216.3 Transcript intron_variant - - - - - - rs5962899 X:107090543 A 11043 NM_052817.2 Transcript intron_variant - - - - - - rs2473632 X:107136497 T CCDS14532.2 CCDS14532.2 Transcript intron_variant - - - - - - rs2473632 X:107136497 T CCDS14533.2 CCDS14533.2 Transcript intron_variant - - - - - - rs2473632 X:107136497 T 11043 NM_012216.3 Transcript intron_variant - - - - - - rs2473632 X:107136497 T 11043 NM_052817.2 Transcript intron_variant - - - - - - rs2473631 X:107136591 T CCDS14532.2 CCDS14532.2 Transcript intron_variant - - - - - - rs2473631 X:107136591 T CCDS14533.2 CCDS14533.2 Transcript intron_variant - - - - - - rs2473631 X:107136591 T 11043 NM_012216.3 Transcript intron_variant - - - - - - rs2473631 X:107136591 T 11043 NM_052817.2 Transcript intron_variant - - - - - - rs2500127 X:107158764 G CCDS14532.2 CCDS14532.2 Transcript intron_variant - - - - - - rs2500127 X:107158764 G CCDS14533.2 CCDS14533.2 Transcript intron_variant - - - - - - rs2500127 X:107158764 G 11043 NM_012216.3 Transcript intron_variant - - - - - - rs2500127 X:107158764 G 11043 NM_052817.2 Transcript intron_variant - - - - - - rs2500127 X:107158764 G ENSESTG00000017535 ENSESTT00000044124 Transcript upstream_gene_variant - - - - - - DISTANCE=465 rs911925 X:107472753 T ENSESTG00000017756 ENSESTT00000044734 Transcript intron_variant - - - - - - rs911925 X:107472753 T CCDS14542.1 CCDS14542.1 Transcript intron_variant - - - - - - rs911925 X:107472753 T 1288 NM_001847.2 Transcript intron_variant - - - - - - rs911925 X:107472753 T ENSESTG00000017756 ENSESTT00000044816 Transcript intron_variant - - - - - - rs911925 X:107472753 T ENSESTG00000017756 ENSESTT00000044798 Transcript intron_variant - - - - - - rs911925 X:107472753 T CCDS14541.1 CCDS14541.1 Transcript intron_variant - - - - - - rs911925 X:107472753 T 1288 NM_033641.2 Transcript intron_variant - - - - - - rs5929139 X:107908022 A CCDS35366.1 CCDS35366.1 Transcript intron_variant - - - - - - rs5929139 X:107908022 A CCDS14543.1 CCDS14543.1 Transcript intron_variant - - - - - - rs5929139 X:107908022 A 1287 NM_000495.4 Transcript intron_variant - - - - - - rs5929139 X:107908022 A 1287 NM_033380.2 Transcript intron_variant - - - - - - rs5929140 X:107945429 G 1287 NM_000495.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4654 rs5929140 X:107945429 G 1287 NM_033380.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4654 rs5942900 X:108059913 C - - - intergenic_variant - - - - - - rs235071 X:108137823 C - - - intergenic_variant - - - - - - rs839373 X:108873988 C - - - intergenic_variant - - - - - - rs5942619 X:109262511 C 84187 NM_017698.2 Transcript intron_variant - - - - - - rs5942619 X:109262511 C 84187 NM_032227.3 Transcript intron_variant - - - - - - rs5942619 X:109262511 C CCDS14550.2 CCDS14550.2 Transcript intron_variant - - - - - - rs5942619 X:109262511 C ENSESTG00000030192 ENSESTT00000076027 Transcript intron_variant - - - - - - rs4893453 X:109673965 G ENSESTG00000018189 ENSESTT00000045825 Transcript intron_variant - - - - - - rs4893453 X:109673965 G ENSESTG00000018189 ENSESTT00000045812 Transcript intron_variant - - - - - - rs4893453 X:109673965 G 57529 NM_020769.2 Transcript intron_variant - - - - - - rs4893453 X:109673965 G 9949 NM_001171689.1 Transcript intron_variant - - - - - - rs4893399 X:110139664 A - - - intergenic_variant - - - - - - rs1416598 X:110365098 T ENSESTG00000017880 ENSESTT00000045028 Transcript upstream_gene_variant - - - - - - DISTANCE=3815 rs1416598 X:110365098 T CCDS48151.1 CCDS48151.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1234 rs1416598 X:110365098 T ENSESTG00000017808 ENSESTT00000044908 Transcript intron_variant - - - - - - rs1416598 X:110365098 T CCDS48153.1 CCDS48153.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1234 rs1416598 X:110365098 T CCDS48152.1 CCDS48152.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1234 rs1416598 X:110365098 T 5063 NM_001128172.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1207 rs1416598 X:110365098 T 5063 NM_001128168.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1207 rs1416598 X:110365098 T ENSESTG00000017808 ENSESTT00000044891 Transcript intron_variant - - - - - - rs1416598 X:110365098 T ENSESTG00000017808 ENSESTT00000044865 Transcript intron_variant - - - - - - rs1416598 X:110365098 T 5063 NM_002578.3 Transcript intron_variant - - - - - - rs1416598 X:110365098 T ENSESTG00000017808 ENSESTT00000045002 Transcript intron_variant - - - - - - rs1416598 X:110365098 T ENSESTG00000017808 ENSESTT00000044958 Transcript intron_variant - - - - - - rs1416598 X:110365098 T 5063 NM_001128167.1 Transcript intron_variant - - - - - - rs1416598 X:110365098 T CCDS14554.1 CCDS14554.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1234 rs1416598 X:110365098 T ENSESTG00000017808 ENSESTT00000044850 Transcript intron_variant - - - - - - rs1416598 X:110365098 T 5063 NM_001128173.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1207 rs1416598 X:110365098 T 5063 NM_001128166.1 Transcript intron_variant - - - - - - rs2499928 X:110824134 T - - - intergenic_variant - - - - - - rs758030 X:111101179 C 7224 NM_012471.2 Transcript intron_variant - - - - - - rs758030 X:111101179 C CCDS14561.1 CCDS14561.1 Transcript intron_variant - - - - - - rs5943231 X:111256709 A 7224 NM_012471.2 Transcript intron_variant - - - - - - rs5943231 X:111256709 A ENSESTG00000007060 ENSESTT00000017881 Transcript intron_variant - - - - - - rs1033461 X:111363469 T 340595 NM_001004308.2 Transcript intron_variant - - - - - - rs5929481 X:111942835 A ENSESTG00000020794 ENSESTT00000052129 Transcript intron_variant - - - - - - rs5929512 X:112244641 G - - - intergenic_variant - - - - - - rs5929283 X:112547801 A - - - intergenic_variant - - - - - - rs5929285 X:112553994 G - - - intergenic_variant - - - - - - rs4829567 X:112563286 T - - - intergenic_variant - - - - - - rs4427324 X:112569776 T - - - intergenic_variant - - - - - - rs5929611 X:112576719 G - - - intergenic_variant - - - - - - rs6568217 X:113197164 G - - - intergenic_variant - - - - - - rs9698258 X:113329324 T - - - intergenic_variant - - - - - - rs10871957 X:113474271 A - - - intergenic_variant - - - - - - rs4481784 X:114437713 G 57631 NM_001243963.1 Transcript intron_variant - - - - - - rs4481784 X:114437713 G 57631 NM_020871.3 Transcript intron_variant - - - - - - rs4481784 X:114437713 G ENSESTG00000008203 ENSESTT00000020743 Transcript intron_variant - - - - - - rs4481784 X:114437713 G CCDS59175.1 CCDS59175.1 Transcript intron_variant - - - - - - rs4481784 X:114437713 G CCDS48155.1 CCDS48155.1 Transcript intron_variant - - - - - - rs4369154 X:114463510 G 57631 NM_001243963.1 Transcript intron_variant - - - - - - rs4369154 X:114463510 G 57631 NM_020871.3 Transcript intron_variant - - - - - - rs4369154 X:114463510 G ENSESTG00000008203 ENSESTT00000020743 Transcript intron_variant - - - - - - rs4369154 X:114463510 G CCDS59175.1 CCDS59175.1 Transcript intron_variant - - - - - - rs4369154 X:114463510 G CCDS48155.1 CCDS48155.1 Transcript intron_variant - - - - - - rs1321126 X:114508143 C - - - intergenic_variant - - - - - - rs5946312 X:114531362 A ENSESTG00000016708 ENSESTT00000041905 Transcript intron_variant - - - - - - rs5946312 X:114531362 A CCDS14567.1 CCDS14567.1 Transcript intron_variant - - - - - - rs5946312 X:114531362 A ENSESTG00000016708 ENSESTT00000041917 Transcript intron_variant - - - - - - rs5946312 X:114531362 A ENSESTG00000016708 ENSESTT00000041913 Transcript intron_variant - - - - - - rs5946312 X:114531362 A 51213 NM_016383.3 Transcript intron_variant - - - - - - rs11798114 X:114592261 A - ENSR00001491154 RegulatoryFeature regulatory_region_variant - - - - - - rs11798114 X:114592261 A - - - intergenic_variant - - - - - - rs2894765 X:114646368 C - - - intergenic_variant - - - - - - rs2207051 X:114673930 T - - - intergenic_variant - - - - - - rs6520217 X:115071807 G ENSESTG00000017077 ENSESTT00000042906 Transcript intron_variant - - - - - - rs6520217 X:115071807 G ENSESTG00000017077 ENSESTT00000042899 Transcript intron_variant - - - - - - rs2206629 X:115505715 G - - - intergenic_variant - - - - - - rs5905297 X:115621190 A - - - intergenic_variant - - - - - - rs5909547 X:115991813 G - - - intergenic_variant - - - - - - rs5910744 X:116137304 T - - - intergenic_variant - - - - - - rs5956241 X:116207820 C - - - intergenic_variant - - - - - - rs5956253 X:116216187 C - - - intergenic_variant - - - - - - rs534688 X:116343986 G - - - intergenic_variant - - - - - - rs1990108 X:116569947 A - - - intergenic_variant - - - - - - rs4240010 X:116650250 C - - - intergenic_variant - - - - - - rs1298038 X:116812330 A - - - intergenic_variant - - - - - - rs2008480 X:116974164 A - - - intergenic_variant - - - - - - rs5910301 X:117327967 C - - - intergenic_variant - - - - - - rs2802910 X:117330427 T - - - intergenic_variant - - - - - - rs1781992 X:117466260 A - - - intergenic_variant - - - - - - rs5910351 X:117584008 A CCDS55482.1 CCDS55482.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1058 rs5910351 X:117584008 A CCDS55483.1 CCDS55483.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1058 rs5910351 X:117584008 A 54521 NM_001184965.1 Transcript downstream_gene_variant - - - - - - DISTANCE=84 rs5910351 X:117584008 A CCDS14572.1 CCDS14572.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1058 rs5910351 X:117584008 A 54521 NM_001184966.1 Transcript downstream_gene_variant - - - - - - DISTANCE=84 rs5910351 X:117584008 A 54521 NM_019045.4 Transcript downstream_gene_variant - - - - - - DISTANCE=84 rs5910351 X:117584008 A ENSESTG00000028313 ENSESTT00000071497 Transcript downstream_gene_variant - - - - - - DISTANCE=112 rs5910351 X:117584008 A ENSESTG00000028313 ENSESTT00000071503 Transcript downstream_gene_variant - - - - - - DISTANCE=112 rs5910351 X:117584008 A ENSESTG00000029154 ENSESTT00000073378 Transcript intron_variant - - - - - - rs2430201 X:117940586 A - - - intergenic_variant - - - - - - rs5910506 X:118206659 C - - - intergenic_variant - - - - - - rs5910577 X:118567579 T CCDS14577.1 CCDS14577.1 Transcript intron_variant - - - - - - rs5910577 X:118567579 T ENSESTG00000000960 ENSESTT00000002307 Transcript intron_variant - - - - - - rs5910577 X:118567579 T ENSESTG00000000960 ENSESTT00000002320 Transcript intron_variant - - - - - - rs5910577 X:118567579 T ENSESTG00000000960 ENSESTT00000002306 Transcript intron_variant - - - - - - rs5910577 X:118567579 T 203427 NM_145305.2 Transcript intron_variant - - - - - - rs5910577 X:118567579 T ENSESTG00000000960 ENSESTT00000002318 Transcript intron_variant - - - - - - rs5910577 X:118567579 T ENSESTG00000000960 ENSESTT00000002309 Transcript intron_variant - - - - - - rs2496215 X:118927378 G 6170 NM_001000.2 Transcript upstream_gene_variant - - - - - - DISTANCE=1772 rs2496215 X:118927378 G CCDS14586.1 CCDS14586.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1839 rs5956205 X:119456947 A - - - intergenic_variant - - - - - - rs5957440 X:119820527 C - - - intergenic_variant - - - - - - rs5911026 X:119985614 A - - - intergenic_variant - - - - - - rs5911027 X:119985618 T - - - intergenic_variant - - - - - - rs5911080 X:120240247 A - - - intergenic_variant - - - - - - rs5911090 X:120271534 G - - - intergenic_variant - - - - - - rs4825440 X:120514691 G - - - intergenic_variant - - - - - - rs1522885 X:120648392 T - - - intergenic_variant - - - - - - rs1935213 X:121027929 C - - - intergenic_variant - - - - - - rs1488338 X:121212590 T ENSESTG00000023511 ENSESTT00000059270 Transcript intron_variant - - - - - - rs2715567 X:121224016 C ENSESTG00000023511 ENSESTT00000059270 Transcript intron_variant - - - - - - rs1166808 X:121297776 A - - - intergenic_variant - - - - - - rs6607990 X:121698057 C - - - intergenic_variant - - - - - - rs1840362 X:121765944 A - - - intergenic_variant - - - - - - rs6655715 X:122295313 G - - - intergenic_variant - - - - - - rs987459 X:122515468 C 2892 NM_007325.4 Transcript intron_variant - - - - - - rs987459 X:122515468 C CCDS14605.1 CCDS14605.1 Transcript intron_variant - - - - - - rs987459 X:122515468 C ENSESTG00000014814 ENSESTT00000037103 Transcript intron_variant - - - - - - rs987459 X:122515468 C 2892 NM_000828.4 Transcript intron_variant - - - - - - rs987459 X:122515468 C CCDS14604.1 CCDS14604.1 Transcript intron_variant - - - - - - rs6608083 X:122521780 T 2892 NM_007325.4 Transcript intron_variant - - - - - - rs6608083 X:122521780 T CCDS14605.1 CCDS14605.1 Transcript intron_variant - - - - - - rs6608083 X:122521780 T ENSESTG00000014814 ENSESTT00000037103 Transcript intron_variant - - - - - - rs6608083 X:122521780 T 2892 NM_000828.4 Transcript intron_variant - - - - - - rs6608083 X:122521780 T CCDS14604.1 CCDS14604.1 Transcript intron_variant - - - - - - rs5911691 X:122843807 G 57187 NM_001081550.1 Transcript intron_variant - - - - - - rs5911691 X:122843807 G ENSESTG00000015018 ENSESTT00000037700 Transcript intron_variant - - - - - - rs5911691 X:122843807 G CCDS43988.1 CCDS43988.1 Transcript intron_variant - - - - - - rs1033687 X:123077755 A - - - intergenic_variant - - - - - - rs2843510 X:123640698 A CCDS55488.1 CCDS55488.1 Transcript intron_variant - - - - - - rs2843510 X:123640698 A 10178 NM_001163278.1 Transcript intron_variant - - - - - - rs2843510 X:123640698 A 10178 NM_014253.3 Transcript intron_variant - - - - - - rs2843510 X:123640698 A CCDS14609.1 CCDS14609.1 Transcript intron_variant - - - - - - rs2843510 X:123640698 A 10178 NM_001163279.1 Transcript intron_variant - - - - - - rs2843504 X:123726544 C CCDS55488.1 CCDS55488.1 Transcript intron_variant - - - - - - rs2843504 X:123726544 C 10178 NM_001163278.1 Transcript intron_variant - - - - - - rs2843504 X:123726544 C 10178 NM_014253.3 Transcript intron_variant - - - - - - rs2843504 X:123726544 C CCDS14609.1 CCDS14609.1 Transcript intron_variant - - - - - - rs2843504 X:123726544 C 10178 NM_001163279.1 Transcript intron_variant - - - - - - rs2858402 X:123730991 C CCDS55488.1 CCDS55488.1 Transcript intron_variant - - - - - - rs2858402 X:123730991 C 10178 NM_001163278.1 Transcript intron_variant - - - - - - rs2858402 X:123730991 C 10178 NM_014253.3 Transcript intron_variant - - - - - - rs2858402 X:123730991 C CCDS14609.1 CCDS14609.1 Transcript intron_variant - - - - - - rs2858402 X:123730991 C 10178 NM_001163279.1 Transcript intron_variant - - - - - - rs1894558 X:123799054 G ENSESTG00000000607 ENSESTT00000001443 Transcript intron_variant - - - - - - rs1894558 X:123799054 G CCDS55488.1 CCDS55488.1 Transcript intron_variant - - - - - - rs1894558 X:123799054 G 10178 NM_001163278.1 Transcript intron_variant - - - - - - rs1894558 X:123799054 G 10178 NM_014253.3 Transcript intron_variant - - - - - - rs1894558 X:123799054 G CCDS14609.1 CCDS14609.1 Transcript intron_variant - - - - - - rs1894558 X:123799054 G 10178 NM_001163279.1 Transcript intron_variant - - - - - - rs5956675 X:123807306 G ENSESTG00000000607 ENSESTT00000001443 Transcript upstream_gene_variant - - - - - - DISTANCE=1705 rs5956675 X:123807306 G CCDS55488.1 CCDS55488.1 Transcript intron_variant - - - - - - rs5956675 X:123807306 G 10178 NM_001163278.1 Transcript intron_variant - - - - - - rs5956675 X:123807306 G 10178 NM_014253.3 Transcript intron_variant - - - - - - rs5956675 X:123807306 G CCDS14609.1 CCDS14609.1 Transcript intron_variant - - - - - - rs5956675 X:123807306 G 10178 NM_001163279.1 Transcript intron_variant - - - - - - rs1894514 X:124028732 T CCDS55488.1 CCDS55488.1 Transcript intron_variant - - - - - - rs1894514 X:124028732 T 10178 NM_001163278.1 Transcript intron_variant - - - - - - rs1894514 X:124028732 T ENSESTG00000000603 ENSESTT00000001442 Transcript downstream_gene_variant - - - - - - DISTANCE=1104 rs1894514 X:124028732 T 10178 NM_014253.3 Transcript intron_variant - - - - - - rs1894514 X:124028732 T CCDS14609.1 CCDS14609.1 Transcript intron_variant - - - - - - rs1894514 X:124028732 T 10178 NM_001163279.1 Transcript intron_variant - - - - - - rs4825922 X:124048499 C CCDS55488.1 CCDS55488.1 Transcript intron_variant - - - - - - rs4825922 X:124048499 C 10178 NM_001163278.1 Transcript intron_variant - - - - - - rs4825922 X:124048499 C ENSESTG00000000603 ENSESTT00000001442 Transcript intron_variant - - - - - - rs4825922 X:124048499 C 10178 NM_014253.3 Transcript intron_variant - - - - - - rs4825922 X:124048499 C CCDS14609.1 CCDS14609.1 Transcript intron_variant - - - - - - rs4825922 X:124048499 C 10178 NM_001163279.1 Transcript intron_variant - - - - - - rs2001086 X:124063546 C CCDS55488.1 CCDS55488.1 Transcript intron_variant - - - - - - rs2001086 X:124063546 C 10178 NM_001163278.1 Transcript intron_variant - - - - - - rs2001086 X:124063546 C ENSESTG00000000603 ENSESTT00000001442 Transcript intron_variant - - - - - - rs2001086 X:124063546 C 10178 NM_014253.3 Transcript intron_variant - - - - - - rs2001086 X:124063546 C CCDS14609.1 CCDS14609.1 Transcript intron_variant - - - - - - rs2001086 X:124063546 C 10178 NM_001163279.1 Transcript intron_variant - - - - - - rs1041876 X:124074409 C CCDS55488.1 CCDS55488.1 Transcript intron_variant - - - - - - rs1041876 X:124074409 C 10178 NM_001163278.1 Transcript intron_variant - - - - - - rs1041876 X:124074409 C ENSESTG00000000603 ENSESTT00000001442 Transcript intron_variant - - - - - - rs1041876 X:124074409 C 10178 NM_014253.3 Transcript intron_variant - - - - - - rs1041876 X:124074409 C CCDS14609.1 CCDS14609.1 Transcript intron_variant - - - - - - rs1041876 X:124074409 C 10178 NM_001163279.1 Transcript intron_variant - - - - - - rs5911938 X:124114823 T ENSESTG00000000603 ENSESTT00000001442 Transcript intron_variant - - - - - - rs5910133 X:124178636 T - - - intergenic_variant - - - - - - rs5956729 X:124180297 G - - - intergenic_variant - - - - - - rs5910136 X:124190621 A ENSESTG00000000600 ENSESTT00000001435 Transcript upstream_gene_variant - - - - - - DISTANCE=1883 rs2213613 X:124199281 T - - - intergenic_variant - - - - - - rs28526712 X:124201894 A - - - intergenic_variant - - - - - - rs28563897 X:124225418 G - - - intergenic_variant - - - - - - rs4825512 X:124225874 G - - - intergenic_variant - - - - - - rs1005378 X:124229368 T ENSESTG00000000599 ENSESTT00000001430 Transcript downstream_gene_variant - - - - - - DISTANCE=4058 rs2213489 X:124236380 G ENSESTG00000000599 ENSESTT00000001430 Transcript intron_variant - - - - - - rs4825513 X:124243676 A ENSESTG00000000599 ENSESTT00000001430 Transcript intron_variant - - - - - - rs4825514 X:124243743 A ENSESTG00000000599 ENSESTT00000001430 Transcript intron_variant - - - - - - rs5911995 X:124290360 T ENSESTG00000000599 ENSESTT00000001430 Transcript upstream_gene_variant - - - - - - DISTANCE=1897 rs2356541 X:124314265 C - - - intergenic_variant - - - - - - rs6649755 X:124382497 C - - - intergenic_variant - - - - - - rs6423156 X:124417661 G - - - intergenic_variant - - - - - - rs3126309 X:124474124 G - - - intergenic_variant - - - - - - rs1563715 X:124603857 C - - - intergenic_variant - - - - - - rs4829660 X:124606639 C - - - intergenic_variant - - - - - - rs177026 X:124691049 A - - - intergenic_variant - - - - - - rs5932386 X:124723900 C - - - intergenic_variant - - - - - - rs2227042 X:124782061 A - - - intergenic_variant - - - - - - rs2187716 X:124785701 T - - - intergenic_variant - - - - - - rs2205004 X:125180033 A - - - intergenic_variant - - - - - - rs6529587 X:125278898 A - - - intergenic_variant - - - - - - rs1501499 X:125331404 G - - - intergenic_variant - - - - - - rs1936828 X:125418351 G - - - intergenic_variant - - - - - - rs1290560 X:125430535 A - - - intergenic_variant - - - - - - rs1341954 X:125535142 G - - - intergenic_variant - - - - - - rs4829843 X:125561035 G - - - intergenic_variant - - - - - - rs6633899 X:125637326 T - - - intergenic_variant - - - - - - rs2515988 X:125669743 T - - - intergenic_variant - - - - - - rs6635884 X:125851497 G - - - intergenic_variant - - - - - - rs1937537 X:125857195 T - - - intergenic_variant - - - - - - rs4317717 X:125873721 G - - - intergenic_variant - - - - - - rs5930051 X:126067743 G - - - intergenic_variant - - - - - - rs204309 X:126104933 G - - - intergenic_variant - - - - - - rs204350 X:126128436 G - - - intergenic_variant - - - - - - rs204348 X:126132655 A - - - intergenic_variant - - - - - - rs204338 X:126144196 C - - - intergenic_variant - - - - - - rs204336 X:126147659 T - - - intergenic_variant - - - - - - rs204325 X:126163480 G - - - intergenic_variant - - - - - - rs204324 X:126163497 T - - - intergenic_variant - - - - - - rs204319 X:126172286 A - ENSR00000661241 RegulatoryFeature regulatory_region_variant - - - - - - rs204319 X:126172286 A - - - intergenic_variant - - - - - - rs5976491 X:126218707 T - - - intergenic_variant - - - - - - rs5931847 X:126242078 G - - - intergenic_variant - - - - - - rs1291959 X:126272738 C - - - intergenic_variant - - - - - - rs1291987 X:126353997 T - - - intergenic_variant - - - - - - rs2858257 X:126363278 A - - - intergenic_variant - - - - - - rs4433292 X:126529244 C ENSESTG00000032761 ENSESTT00000082750 Transcript downstream_gene_variant - - - - - - DISTANCE=2807 rs5976550 X:126530735 G ENSESTG00000032761 ENSESTT00000082750 Transcript downstream_gene_variant - - - - - - DISTANCE=4298 rs6634596 X:126533525 C - - - intergenic_variant - - - - - - rs4262433 X:126549639 G - - - intergenic_variant - - - - - - rs4581186 X:126567059 G - - - intergenic_variant - - - - - - rs226611 X:126913104 T - - - intergenic_variant - - - - - - rs226612 X:126913823 T - - - intergenic_variant - - - - - - rs226613 X:126914080 C - - - intergenic_variant - - - - - - rs226582 X:126930311 G - - - intergenic_variant - - - - - - rs226579 X:126930557 C - - - intergenic_variant - - - - - - rs2858215 X:126944420 C - - - intergenic_variant - - - - - - rs424681 X:126952843 C - - - intergenic_variant - - - - - - rs366079 X:126953154 A - - - intergenic_variant - - - - - - rs226658 X:126955242 A - - - intergenic_variant - - - - - - rs226653 X:126957739 A - - - intergenic_variant - - - - - - rs226640 X:126964033 T - - - intergenic_variant - - - - - - rs226639 X:126966132 T - - - intergenic_variant - - - - - - rs226634 X:126971471 C - - - intergenic_variant - - - - - - rs432934 X:126974385 G - - - intergenic_variant - - - - - - rs395802 X:126974388 G - - - intergenic_variant - - - - - - rs5932267 X:127106440 G - - - intergenic_variant - - - - - - rs4830063 X:127109137 C - - - intergenic_variant - - - - - - rs2040396 X:127123153 C - - - intergenic_variant - - - - - - rs521086 X:127181884 C CCDS14611.1 CCDS14611.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3171 rs521086 X:127181884 C ENSESTG00000032765 ENSESTT00000082756 Transcript downstream_gene_variant - - - - - - DISTANCE=3998 rs521086 X:127181884 C 139741 NM_138289.3 Transcript downstream_gene_variant - - - - - - DISTANCE=3057 rs669670 X:127182043 G CCDS14611.1 CCDS14611.1 Transcript downstream_gene_variant - - - - - - DISTANCE=3012 rs669670 X:127182043 G ENSESTG00000032765 ENSESTT00000082756 Transcript downstream_gene_variant - - - - - - DISTANCE=3839 rs669670 X:127182043 G 139741 NM_138289.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2898 rs4830064 X:127245696 A - - - intergenic_variant - - - - - - rs240580 X:127496325 G ENSESTG00000019654 ENSESTT00000049286 Transcript intron_variant - - - - - - rs725568 X:127635519 A ENSESTG00000019654 ENSESTT00000049286 Transcript intron_variant - - - - - - rs725569 X:127635761 T ENSESTG00000019654 ENSESTT00000049286 Transcript intron_variant - - - - - - rs1018873 X:127652828 C - ENSR00001491484 RegulatoryFeature regulatory_region_variant - - - - - - rs1018873 X:127652828 C ENSESTG00000019654 ENSESTT00000049286 Transcript intron_variant - - - - - - rs2214073 X:127665505 A ENSESTG00000019654 ENSESTT00000049286 Transcript intron_variant - - - - - - rs2157906 X:127674130 T ENSESTG00000019654 ENSESTT00000049286 Transcript intron_variant - - - - - - rs2106476 X:127678224 T ENSESTG00000019654 ENSESTT00000049286 Transcript intron_variant - - - - - - rs416182 X:127730161 T ENSESTG00000019654 ENSESTT00000049286 Transcript intron_variant - - - - - - rs410929 X:127741853 G - - - intergenic_variant - - - - - - rs761115 X:127849220 T - - - intergenic_variant - - - - - - rs6529403 X:128855635 C - - - intergenic_variant - - - - - - rs4829710 X:129113068 A ENSESTG00000021128 ENSESTT00000053084 Transcript upstream_gene_variant - - - - - - DISTANCE=3540 rs4829710 X:129113068 A ENSESTG00000021128 ENSESTT00000053067 Transcript upstream_gene_variant - - - - - - DISTANCE=3518 rs762949 X:129143019 G CCDS14616.1 CCDS14616.1 Transcript intron_variant - - - - - - rs762949 X:129143019 G ENSESTG00000021128 ENSESTT00000053084 Transcript intron_variant - - - - - - rs762949 X:129143019 G ENSESTG00000021128 ENSESTT00000053067 Transcript intron_variant - - - - - - rs762949 X:129143019 G 63035 NM_021946.4 Transcript intron_variant - - - - - - rs4830173 X:129147079 C CCDS14616.1 CCDS14616.1 Transcript missense_variant 331 331 111 F/L Ttc/Ctc - PolyPhen=unknown;SIFT=tolerated rs4830173 X:129147079 C ENSESTG00000021128 ENSESTT00000053084 Transcript downstream_gene_variant - - - - - - DISTANCE=440 rs4830173 X:129147079 C ENSESTG00000021492 ENSESTT00000053889 Transcript downstream_gene_variant - - - - - - DISTANCE=1585 rs4830173 X:129147079 C ENSESTG00000021494 ENSESTT00000053908 Transcript downstream_gene_variant - - - - - - DISTANCE=1881 rs4830173 X:129147079 C ENSESTG00000021128 ENSESTT00000053067 Transcript missense_variant 528 331 111 F/L Ttc/Ctc - rs4830173 X:129147079 C 63035 NM_021946.4 Transcript missense_variant 375 331 111 F/L Ttc/Ctc - PolyPhen=unknown;SIFT=tolerated rs4830173 X:129147079 C ENSESTG00000021159 ENSESTT00000053236 Transcript upstream_gene_variant - - - - - - DISTANCE=3090 rs209536 X:129286719 A CCDS48167.1 CCDS48167.1 Transcript intron_variant - - - - - - rs209536 X:129286719 A ENSESTG00000021348 ENSESTT00000053783 Transcript intron_variant - - - - - - rs209536 X:129286719 A ENSESTG00000021348 ENSESTT00000053749 Transcript intron_variant - - - - - - rs209536 X:129286719 A CCDS14618.1 CCDS14618.1 Transcript intron_variant - - - - - - rs209536 X:129286719 A 9131 NM_145812.2 Transcript intron_variant - - - - - - rs209536 X:129286719 A 9131 NM_001130847.3 Transcript intron_variant - - - - - - rs209536 X:129286719 A CCDS14619.1 CCDS14619.1 Transcript intron_variant - - - - - - rs209536 X:129286719 A 9131 NM_004208.3 Transcript intron_variant - - - - - - rs209536 X:129286719 A 9131 NM_145813.2 Transcript intron_variant - - - - - - rs209218 X:129381415 G ENSESTG00000021263 ENSESTT00000053486 Transcript intron_variant - - - - - - rs209218 X:129381415 G CCDS14622.1 CCDS14622.1 Transcript intron_variant - - - - - - rs209218 X:129381415 G 55609 NM_017666.4 Transcript intron_variant - - - - - - rs5930391 X:129403238 C - ENSR00000481997 RegulatoryFeature regulatory_region_variant - - - - - - rs5930391 X:129403238 C - MA0058.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=4;MOTIF_NAME=Jaspar_Matrix_Max:MA0058.1;HIGH_INF_POS=Y;MOTIF_SCORE_CHANGE=-0.130 rs5930391 X:129403238 C - PL0007.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=6;MOTIF_NAME=Jaspar_Matrix_Max:PL0007.1;HIGH_INF_POS=Y;MOTIF_SCORE_CHANGE=-0.122 rs5930391 X:129403238 C - MA0058.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=9;MOTIF_NAME=Jaspar_Matrix_Max:MA0058.1;HIGH_INF_POS=Y;MOTIF_SCORE_CHANGE=-0.130 rs5930391 X:129403238 C - PL0014.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=11;MOTIF_NAME=Jaspar_Matrix_mxl-1::mdl-1:PL0014.1;HIGH_INF_POS=Y;MOTIF_SCORE_CHANGE=-0.131 rs5930391 X:129403238 C - PL0007.1 MotifFeature TF_binding_site_variant - - - - - - MOTIF_POS=11;MOTIF_NAME=Jaspar_Matrix_Max:PL0007.1;HIGH_INF_POS=Y;MOTIF_SCORE_CHANGE=-0.122 rs5930391 X:129403238 C ENSESTG00000021263 ENSESTT00000053486 Transcript upstream_gene_variant - - - - - - DISTANCE=365 rs5930391 X:129403238 C 55609 NM_017666.4 Transcript upstream_gene_variant - - - - - - DISTANCE=316 rs5932747 X:129478663 A CCDS14623.1 CCDS14623.1 Transcript intron_variant - - - - - - rs5932747 X:129478663 A ENSESTG00000033664 ENSESTT00000085190 Transcript intron_variant - - - - - - rs5932747 X:129478663 A 9016 NM_003951.2 Transcript intron_variant - - - - - - rs5932747 X:129478663 A 9016 NM_022810.1 Transcript intron_variant - - - - - - rs5932747 X:129478663 A ENSESTG00000033664 ENSESTT00000085207 Transcript intron_variant - - - - - - rs5932747 X:129478663 A ENSESTG00000033664 ENSESTT00000085110 Transcript intron_variant - - - - - - rs5932747 X:129478663 A ENSESTG00000033664 ENSESTT00000085216 Transcript upstream_gene_variant - - - - - - DISTANCE=491 rs5932747 X:129478663 A ENSESTG00000033664 ENSESTT00000085175 Transcript intron_variant - - - - - - rs5932747 X:129478663 A ENSESTG00000033664 ENSESTT00000085164 Transcript intron_variant - - - - - - rs5932747 X:129478663 A CCDS14624.1 CCDS14624.1 Transcript intron_variant - - - - - - rs3986808 X:129612855 G - - - intergenic_variant - - - - - - rs1003847 X:129665357 G - - - intergenic_variant - - - - - - rs3007754 X:129670733 C - - - intergenic_variant - - - - - - rs4830202 X:129919325 A ENSESTG00000033778 ENSESTT00000085415 Transcript intron_variant - - - - - - rs4830202 X:129919325 A ENSESTG00000033778 ENSESTT00000085403 Transcript intron_variant - - - - - - rs4830202 X:129919325 A ENSESTG00000033778 ENSESTT00000085426 Transcript intron_variant - - - - - - rs4830202 X:129919325 A 10495 NM_182314.1 Transcript intron_variant - - - - - - rs4830202 X:129919325 A ENSESTG00000033778 ENSESTT00000085401 Transcript intron_variant - - - - - - rs4830202 X:129919325 A 10495 NM_006375.2 Transcript intron_variant - - - - - - rs4830202 X:129919325 A ENSESTG00000033778 ENSESTT00000085421 Transcript intron_variant - - - - - - rs5932812 X:129937321 A ENSESTG00000033778 ENSESTT00000085403 Transcript intron_variant - - - - - - rs5932812 X:129937321 A ENSESTG00000033778 ENSESTT00000085426 Transcript intron_variant - - - - - - rs5932812 X:129937321 A 10495 NM_182314.1 Transcript intron_variant - - - - - - rs5932812 X:129937321 A ENSESTG00000033778 ENSESTT00000085401 Transcript intron_variant - - - - - - rs5932812 X:129937321 A ENSESTG00000033778 ENSESTT00000085415 Transcript intron_variant - - - - - - rs5932812 X:129937321 A ENSESTG00000033727 ENSESTT00000085279 Transcript splice_region_variant,intron_variant - - - - - - rs5932812 X:129937321 A 10495 NM_006375.2 Transcript intron_variant - - - - - - rs5932812 X:129937321 A ENSESTG00000033778 ENSESTT00000085421 Transcript intron_variant - - - - - - rs1883248 X:130086507 G - ENSR00000261536 RegulatoryFeature regulatory_region_variant - - - - - - rs1883248 X:130086507 G - - - intergenic_variant - - - - - - rs4829720 X:130145469 G - - - intergenic_variant - - - - - - rs2320886 X:131009354 C - - - intergenic_variant - - - - - - rs5975312 X:131130951 C - - - intergenic_variant - - - - - - rs1203742 X:131402773 C ENSESTG00000002532 ENSESTT00000006280 Transcript intron_variant - - - - - - rs1203742 X:131402773 C ENSESTG00000002532 ENSESTT00000006276 Transcript intron_variant - - - - - - rs1203742 X:131402773 C ENSESTG00000002532 ENSESTT00000006271 Transcript intron_variant - - - - - - rs5977679 X:131432380 G ENSESTG00000002532 ENSESTT00000006280 Transcript intron_variant - - - - - - rs5977679 X:131432380 G ENSESTG00000002532 ENSESTT00000006276 Transcript intron_variant - - - - - - rs5977679 X:131432380 G ENSESTG00000002532 ENSESTT00000006271 Transcript intron_variant - - - - - - rs2583498 X:131596103 T 55796 NM_001170704.1 Transcript intron_variant - - - - - - rs2583498 X:131596103 T ENSESTG00000006562 ENSESTT00000016536 Transcript intron_variant - - - - - - rs2583498 X:131596103 T ENSESTG00000006562 ENSESTT00000016538 Transcript intron_variant - - - - - - rs2770694 X:131651440 G - - - intergenic_variant - - - - - - rs858617 X:131819108 A 90161 NM_147175.3 Transcript intron_variant - - - - - - rs858617 X:131819108 A 90161 NM_001077188.1 Transcript intron_variant - - - - - - rs858617 X:131819108 A ENSESTG00000006559 ENSESTT00000016517 Transcript intron_variant - - - - - - rs858617 X:131819108 A CCDS48169.1 CCDS48169.1 Transcript intron_variant - - - - - - rs858617 X:131819108 A CCDS48170.1 CCDS48170.1 Transcript intron_variant - - - - - - rs5933207 X:131956904 C 90161 NM_147175.3 Transcript intron_variant - - - - - - rs5933207 X:131956904 C 90161 NM_001077188.1 Transcript intron_variant - - - - - - rs5933207 X:131956904 C CCDS48169.1 CCDS48169.1 Transcript intron_variant - - - - - - rs5933207 X:131956904 C CCDS48170.1 CCDS48170.1 Transcript intron_variant - - - - - - rs6418952 X:132001832 A 90161 NM_147175.3 Transcript intron_variant - - - - - - rs6418952 X:132001832 A 90161 NM_001077188.1 Transcript intron_variant - - - - - - rs6418952 X:132001832 A CCDS48169.1 CCDS48169.1 Transcript intron_variant - - - - - - rs6418952 X:132001832 A CCDS48170.1 CCDS48170.1 Transcript intron_variant - - - - - - rs5933231 X:132024854 G 90161 NM_147175.3 Transcript intron_variant - - - - - - rs5933231 X:132024854 G 90161 NM_001077188.1 Transcript intron_variant - - - - - - rs5933231 X:132024854 G CCDS48169.1 CCDS48169.1 Transcript intron_variant - - - - - - rs5933231 X:132024854 G CCDS48170.1 CCDS48170.1 Transcript intron_variant - - - - - - rs2315336 X:132028890 G 90161 NM_147175.3 Transcript intron_variant - - - - - - rs2315336 X:132028890 G 90161 NM_001077188.1 Transcript intron_variant - - - - - - rs2315336 X:132028890 G CCDS48169.1 CCDS48169.1 Transcript intron_variant - - - - - - rs2315336 X:132028890 G CCDS48170.1 CCDS48170.1 Transcript intron_variant - - - - - - rs5977780 X:132042361 C 90161 NM_147175.3 Transcript intron_variant - - - - - - rs5977780 X:132042361 C 90161 NM_001077188.1 Transcript intron_variant - - - - - - rs5977780 X:132042361 C CCDS48169.1 CCDS48169.1 Transcript intron_variant - - - - - - rs5977780 X:132042361 C CCDS48170.1 CCDS48170.1 Transcript intron_variant - - - - - - rs187887343 X:132139846 C - - - intergenic_variant - - - - - - rs886140 X:132646173 T - - - intergenic_variant - - - - - - rs1029390 X:132646448 C - - - intergenic_variant - - - - - - rs175225 X:133130097 A - - - intergenic_variant - - - - - - rs175226 X:133134597 G - - - intergenic_variant - - - - - - rs5933376 X:133188562 A - - - intergenic_variant - - - - - - rs175328 X:133249104 C - - - intergenic_variant - - - - - - rs2428577 X:133379551 T CCDS48171.1 CCDS48171.1 Transcript synonymous_variant 721 721 241 L Cta/Tta - rs2428577 X:133379551 T 347475 NM_001101357.1 Transcript synonymous_variant 1042 721 241 L Cta/Tta - rs117407 X:133609110 A CCDS14641.1 CCDS14641.1 Transcript intron_variant - - - - - - rs117407 X:133609110 A ENSESTG00000014256 ENSESTT00000035704 Transcript intron_variant - - - - - - rs117407 X:133609110 A 3251 NM_000194.2 Transcript intron_variant - - - - - - rs4240103 X:134462418 C - ENSR00001491760 RegulatoryFeature regulatory_region_variant - - - - - - rs4240103 X:134462418 C - - - intergenic_variant - - - - - - rs2531376 X:134518385 C - - - intergenic_variant - - - - - - rs66844215 X:135187353 G - - - intergenic_variant - - - - - - rs5930924 X:135373633 A - - - intergenic_variant - - - - - - rs5975732 X:135504200 C - - - intergenic_variant - - - - - - rs1210106 X:135622777 T 51442 NM_016267.3 Transcript intron_variant - - - - - - rs1210106 X:135622777 T CCDS14658.1 CCDS14658.1 Transcript intron_variant - - - - - - rs1210106 X:135622777 T ENSESTG00000014387 ENSESTT00000036007 Transcript intron_variant - - - - - - rs1190731 X:136063455 G - - - intergenic_variant - - - - - - rs1211203 X:136164809 C - - - intergenic_variant - - - - - - rs1334493 X:136269513 A - - - intergenic_variant - - - - - - rs4829609 X:136295203 A - - - intergenic_variant - - - - - - rs5975890 X:136350954 T - - - intergenic_variant - - - - - - rs5975906 X:136398559 C - - - intergenic_variant - - - - - - rs923329 X:137390211 G - - - intergenic_variant - - - - - - rs4472670 X:137557082 T - - - intergenic_variant - - - - - - rs5931451 X:137563508 G - - - intergenic_variant - - - - - - rs5976185 X:137749997 T CCDS55512.1 CCDS55512.1 Transcript intron_variant - - - - - - rs5976185 X:137749997 T 2258 NM_033642.2 Transcript intron_variant - - - - - - rs5976185 X:137749997 T CCDS14665.1 CCDS14665.1 Transcript intron_variant - - - - - - rs5976185 X:137749997 T 2258 NM_004114.3 Transcript intron_variant - - - - - - rs5976185 X:137749997 T ENSESTG00000004584 ENSESTT00000011550 Transcript intron_variant - - - - - - rs5976185 X:137749997 T CCDS55513.1 CCDS55513.1 Transcript intron_variant - - - - - - rs5976185 X:137749997 T 2258 NM_001139498.1 Transcript intron_variant - - - - - - rs5976185 X:137749997 T 2258 NM_001139500.1 Transcript intron_variant - - - - - - rs5976185 X:137749997 T CCDS14664.1 CCDS14664.1 Transcript intron_variant - - - - - - rs5976185 X:137749997 T 2258 NM_001139502.1 Transcript intron_variant - - - - - - rs5976185 X:137749997 T 2258 NM_001139501.1 Transcript intron_variant - - - - - - rs5976185 X:137749997 T 574507 NR_030229.1 Transcript upstream_gene_variant - - - - - - DISTANCE=43 rs5976185 X:137749997 T ENSESTG00000004584 ENSESTT00000011543 Transcript intron_variant - - - - - - rs5976185 X:137749997 T CCDS55511.1 CCDS55511.1 Transcript intron_variant - - - - - - rs762930 X:137824085 G CCDS55512.1 CCDS55512.1 Transcript intron_variant - - - - - - rs762930 X:137824085 G 2258 NM_033642.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2570 rs762930 X:137824085 G CCDS55513.1 CCDS55513.1 Transcript intron_variant - - - - - - rs762930 X:137824085 G 2258 NM_001139498.1 Transcript intron_variant - - - - - - rs762930 X:137824085 G 2258 NM_001139500.1 Transcript intron_variant - - - - - - rs762930 X:137824085 G CCDS14664.1 CCDS14664.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2654 rs762930 X:137824085 G 2258 NM_001139502.1 Transcript intron_variant - - - - - - rs762930 X:137824085 G 2258 NM_001139501.1 Transcript intron_variant - - - - - - rs762930 X:137824085 G ENSESTG00000004584 ENSESTT00000011543 Transcript upstream_gene_variant - - - - - - DISTANCE=2634 rs762930 X:137824085 G CCDS55511.1 CCDS55511.1 Transcript intron_variant - - - - - - rs2858542 X:137828368 C CCDS55512.1 CCDS55512.1 Transcript intron_variant - - - - - - rs2858542 X:137828368 C 2258 NM_001139501.1 Transcript intron_variant - - - - - - rs2858542 X:137828368 C 2258 NM_001139502.1 Transcript intron_variant - - - - - - rs2858542 X:137828368 C CCDS55513.1 CCDS55513.1 Transcript intron_variant - - - - - - rs2858542 X:137828368 C CCDS55511.1 CCDS55511.1 Transcript intron_variant - - - - - - rs2858542 X:137828368 C 2258 NM_001139498.1 Transcript intron_variant - - - - - - rs2858542 X:137828368 C 2258 NM_001139500.1 Transcript intron_variant - - - - - - rs1016116 X:138172458 C CCDS55512.1 CCDS55512.1 Transcript intron_variant - - - - - - rs1016116 X:138172458 C 2258 NM_001139501.1 Transcript intron_variant - - - - - - rs1016116 X:138172458 C CCDS55513.1 CCDS55513.1 Transcript intron_variant - - - - - - rs1016116 X:138172458 C 2258 NM_001139498.1 Transcript intron_variant - - - - - - rs1016116 X:138172458 C 2258 NM_001139500.1 Transcript intron_variant - - - - - - rs2367513 X:138370433 T - - - intergenic_variant - - - - - - rs5908675 X:139007888 C ENSESTG00000029205 ENSESTT00000073597 Transcript intron_variant - - - - - - rs5908675 X:139007888 C 574508 NR_030230.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1498 rs5908675 X:139007888 C ENSESTG00000029205 ENSESTT00000073610 Transcript intron_variant - - - - - - rs5908675 X:139007888 C ENSESTG00000029205 ENSESTT00000073624 Transcript intron_variant - - - - - - rs2496267 X:139204872 T - - - intergenic_variant - - - - - - rs615679 X:139257825 T - - - intergenic_variant - - - - - - rs1323326 X:139469563 C - - - intergenic_variant - - - - - - rs4824943 X:139475587 A - - - intergenic_variant - - - - - - rs6528704 X:139497858 C - - - intergenic_variant - - - - - - rs5909059 X:139564734 C - - - intergenic_variant - - - - - - rs5909063 X:139580652 G 6658 NM_005634.2 Transcript downstream_gene_variant - - - - - - DISTANCE=4500 rs203646 X:139616574 A - - - intergenic_variant - - - - - - rs2207506 X:139824455 C ENSESTG00000026231 ENSESTT00000066103 Transcript intron_variant - - - - - - rs205601 X:140816994 A - - - intergenic_variant - - - - - - rs6528939 X:141083818 A - - - intergenic_variant - - - - - - rs5908119 X:141157723 C - - - intergenic_variant - - - - - - rs4825132 X:141672697 A - - - intergenic_variant - - - - - - rs5953782 X:141926300 T - - - intergenic_variant - - - - - - rs5953811 X:142229504 C - - - intergenic_variant - - - - - - rs2206025 X:142233408 G - - - intergenic_variant - - - - - - rs3975397 X:142268521 G - - - intergenic_variant - - - - - - rs2494527 X:142319748 C - - - intergenic_variant - - - - - - rs5953831 X:142466889 C - - - intergenic_variant - - - - - - rs4825163 X:142485805 C - - - intergenic_variant - - - - - - rs2223356 X:142496575 A - - - intergenic_variant - - - - - - rs147209646 X:143316682 G - - - intergenic_variant - - - - - - rs2142784 X:143967811 A - - - intergenic_variant - - - - - - rs28407528 X:143980564 C - - - intergenic_variant - - - - - - rs2382940 X:143996698 T - - - intergenic_variant - - - - - - rs4827750 X:144038542 T - - - intergenic_variant - - - - - - rs1143724 X:144593038 T - - - intergenic_variant - - - - - - rs1174178 X:144605321 G - - - intergenic_variant - - - - - - rs1151963 X:144638195 C - - - intergenic_variant - - - - - - rs989992 X:144893538 T ENSESTG00000015252 ENSESTT00000038187 Transcript intron_variant - - - - - - rs926974 X:144895553 T 84631 NM_001144003.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3794 rs926974 X:144895553 T ENSESTG00000015252 ENSESTT00000038187 Transcript intron_variant - - - - - - rs926974 X:144895553 T 84631 NM_001144005.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3794 rs926974 X:144895553 T 84631 NM_032539.4 Transcript upstream_gene_variant - - - - - - DISTANCE=3794 rs926974 X:144895553 T 84631 NM_001144004.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3794 rs5919998 X:145143966 C - - - intergenic_variant - - - - - - rs5920013 X:145215492 C - - - intergenic_variant - - - - - - rs4827695 X:145313102 T - - - intergenic_variant - - - - - - rs2207935 X:145535810 A - - - intergenic_variant - - - - - - rs5966272 X:145672998 C - - - intergenic_variant - - - - - - rs447617 X:145780770 G - - - intergenic_variant - - - - - - rs5919731 X:145853587 A - - - intergenic_variant - - - - - - rs6525778 X:145981593 G - - - intergenic_variant - - - - - - rs5905020 X:146329484 T 100422847 NR_036173.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2185 rs655906 X:146578555 G - - - intergenic_variant - - - - - - rs981655 X:146715837 A - - - intergenic_variant - - - - - - rs2193157 X:146771881 T - - - intergenic_variant - - - - - - rs2197708 X:146891294 G - - - intergenic_variant - - - - - - rs1270094 X:147001336 T 2332 NM_001185082.1 Transcript intron_variant - - - - - - rs1270094 X:147001336 T 2332 NM_001185076.1 Transcript intron_variant - - - - - - rs1270094 X:147001336 T 2332 NR_033699.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270094 X:147001336 T 100126270 NR_024499.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270094 X:147001336 T ENSESTG00000004041 ENSESTT00000010227 Transcript intron_variant - - - - - - rs1270094 X:147001336 T ENSESTG00000004041 ENSESTT00000010224 Transcript intron_variant - - - - - - rs1270094 X:147001336 T 2332 NM_001185081.1 Transcript intron_variant - - - - - - rs1270094 X:147001336 T 100126270 NR_024502.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270094 X:147001336 T CCDS55519.1 CCDS55519.1 Transcript intron_variant - - - - - - rs1270094 X:147001336 T 2332 NM_002024.5 Transcript intron_variant - - - - - - rs1270094 X:147001336 T 100126270 NR_024500.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270094 X:147001336 T 2332 NM_001185075.1 Transcript intron_variant - - - - - - rs1270094 X:147001336 T CCDS14682.1 CCDS14682.1 Transcript intron_variant - - - - - - rs1270094 X:147001336 T CCDS55518.1 CCDS55518.1 Transcript intron_variant - - - - - - rs1270094 X:147001336 T 2332 NR_033700.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270094 X:147001336 T 100126270 NR_024501.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270094 X:147001336 T 100126270 NR_024503.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270093 X:147001504 T 2332 NM_001185082.1 Transcript intron_variant - - - - - - rs1270093 X:147001504 T 2332 NM_001185076.1 Transcript intron_variant - - - - - - rs1270093 X:147001504 T 2332 NR_033699.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270093 X:147001504 T 100126270 NR_024499.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270093 X:147001504 T ENSESTG00000004041 ENSESTT00000010227 Transcript intron_variant - - - - - - rs1270093 X:147001504 T ENSESTG00000004041 ENSESTT00000010224 Transcript intron_variant - - - - - - rs1270093 X:147001504 T 2332 NM_001185081.1 Transcript intron_variant - - - - - - rs1270093 X:147001504 T 100126270 NR_024502.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270093 X:147001504 T CCDS55519.1 CCDS55519.1 Transcript intron_variant - - - - - - rs1270093 X:147001504 T 2332 NM_002024.5 Transcript intron_variant - - - - - - rs1270093 X:147001504 T 100126270 NR_024500.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270093 X:147001504 T 2332 NM_001185075.1 Transcript intron_variant - - - - - - rs1270093 X:147001504 T CCDS14682.1 CCDS14682.1 Transcript intron_variant - - - - - - rs1270093 X:147001504 T CCDS55518.1 CCDS55518.1 Transcript intron_variant - - - - - - rs1270093 X:147001504 T 2332 NR_033700.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270093 X:147001504 T 100126270 NR_024501.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270093 X:147001504 T 100126270 NR_024503.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270092 X:147003564 C 2332 NM_001185082.1 Transcript intron_variant - - - - - - rs1270092 X:147003564 C 2332 NM_001185076.1 Transcript intron_variant - - - - - - rs1270092 X:147003564 C 2332 NR_033699.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270092 X:147003564 C 100126270 NR_024499.1 Transcript non_coding_exon_variant,nc_transcript_variant 113 - - - - - rs1270092 X:147003564 C ENSESTG00000004041 ENSESTT00000010227 Transcript intron_variant - - - - - - rs1270092 X:147003564 C ENSESTG00000004041 ENSESTT00000010224 Transcript intron_variant - - - - - - rs1270092 X:147003564 C 2332 NM_001185081.1 Transcript intron_variant - - - - - - rs1270092 X:147003564 C 100126270 NR_024502.1 Transcript non_coding_exon_variant,nc_transcript_variant 113 - - - - - rs1270092 X:147003564 C CCDS55519.1 CCDS55519.1 Transcript intron_variant - - - - - - rs1270092 X:147003564 C 2332 NM_002024.5 Transcript intron_variant - - - - - - rs1270092 X:147003564 C 100126270 NR_024500.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270092 X:147003564 C 2332 NM_001185075.1 Transcript intron_variant - - - - - - rs1270092 X:147003564 C CCDS14682.1 CCDS14682.1 Transcript intron_variant - - - - - - rs1270092 X:147003564 C CCDS55518.1 CCDS55518.1 Transcript intron_variant - - - - - - rs1270092 X:147003564 C 2332 NR_033700.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270092 X:147003564 C 100126270 NR_024501.1 Transcript non_coding_exon_variant,nc_transcript_variant 113 - - - - - rs1270092 X:147003564 C 100126270 NR_024503.1 Transcript non_coding_exon_variant,nc_transcript_variant 113 - - - - - rs1270091 X:147005273 T 2332 NM_001185082.1 Transcript intron_variant - - - - - - rs1270091 X:147005273 T 2332 NM_001185076.1 Transcript intron_variant - - - - - - rs1270091 X:147005273 T 2332 NR_033699.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270091 X:147005273 T 100126270 NR_024499.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1597 rs1270091 X:147005273 T ENSESTG00000004041 ENSESTT00000010227 Transcript intron_variant - - - - - - rs1270091 X:147005273 T ENSESTG00000004041 ENSESTT00000010224 Transcript intron_variant - - - - - - rs1270091 X:147005273 T 2332 NM_001185081.1 Transcript intron_variant - - - - - - rs1270091 X:147005273 T 100126270 NR_024502.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1597 rs1270091 X:147005273 T CCDS55519.1 CCDS55519.1 Transcript intron_variant - - - - - - rs1270091 X:147005273 T 2332 NM_002024.5 Transcript intron_variant - - - - - - rs1270091 X:147005273 T 100126270 NR_024500.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1597 rs1270091 X:147005273 T 2332 NM_001185075.1 Transcript intron_variant - - - - - - rs1270091 X:147005273 T CCDS14682.1 CCDS14682.1 Transcript intron_variant - - - - - - rs1270091 X:147005273 T CCDS55518.1 CCDS55518.1 Transcript intron_variant - - - - - - rs1270091 X:147005273 T 2332 NR_033700.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs1270091 X:147005273 T 100126270 NR_024501.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1597 rs1270091 X:147005273 T 100126270 NR_024503.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1597 rs4824232 X:147014960 T 2332 NM_001185082.1 Transcript intron_variant - - - - - - rs4824232 X:147014960 T CCDS55519.1 CCDS55519.1 Transcript intron_variant - - - - - - rs4824232 X:147014960 T 2332 NM_002024.5 Transcript intron_variant - - - - - - rs4824232 X:147014960 T 2332 NM_001185076.1 Transcript intron_variant - - - - - - rs4824232 X:147014960 T 2332 NR_033699.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4824232 X:147014960 T 2332 NM_001185075.1 Transcript intron_variant - - - - - - rs4824232 X:147014960 T ENSESTG00000004041 ENSESTT00000010227 Transcript intron_variant - - - - - - rs4824232 X:147014960 T 2332 NM_001185081.1 Transcript intron_variant - - - - - - rs4824232 X:147014960 T ENSESTG00000004041 ENSESTT00000010224 Transcript intron_variant - - - - - - rs4824232 X:147014960 T CCDS14682.1 CCDS14682.1 Transcript intron_variant - - - - - - rs4824232 X:147014960 T CCDS55518.1 CCDS55518.1 Transcript intron_variant - - - - - - rs4824232 X:147014960 T ENSESTG00000004041 ENSESTT00000010230 Transcript intron_variant - - - - - - rs4824232 X:147014960 T 2332 NR_033700.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4824233 X:147015021 T 2332 NM_001185082.1 Transcript intron_variant - - - - - - rs4824233 X:147015021 T CCDS55519.1 CCDS55519.1 Transcript intron_variant - - - - - - rs4824233 X:147015021 T 2332 NM_002024.5 Transcript intron_variant - - - - - - rs4824233 X:147015021 T 2332 NM_001185076.1 Transcript intron_variant - - - - - - rs4824233 X:147015021 T 2332 NR_033699.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs4824233 X:147015021 T 2332 NM_001185075.1 Transcript intron_variant - - - - - - rs4824233 X:147015021 T ENSESTG00000004041 ENSESTT00000010227 Transcript intron_variant - - - - - - rs4824233 X:147015021 T 2332 NM_001185081.1 Transcript intron_variant - - - - - - rs4824233 X:147015021 T ENSESTG00000004041 ENSESTT00000010224 Transcript intron_variant - - - - - - rs4824233 X:147015021 T CCDS14682.1 CCDS14682.1 Transcript intron_variant - - - - - - rs4824233 X:147015021 T CCDS55518.1 CCDS55518.1 Transcript intron_variant - - - - - - rs4824233 X:147015021 T ENSESTG00000004041 ENSESTT00000010230 Transcript intron_variant - - - - - - rs4824233 X:147015021 T 2332 NR_033700.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5904816 X:147026266 T ENSESTG00000004041 ENSESTT00000010237 Transcript downstream_gene_variant - - - - - - DISTANCE=697 rs5904816 X:147026266 T 2332 NM_001185082.1 Transcript intron_variant - - - - - - rs5904816 X:147026266 T 2332 NM_001185076.1 Transcript intron_variant - - - - - - rs5904816 X:147026266 T 2332 NR_033699.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5904816 X:147026266 T ENSESTG00000004041 ENSESTT00000010256 Transcript intron_variant - - - - - - rs5904816 X:147026266 T ENSESTG00000004041 ENSESTT00000010261 Transcript upstream_gene_variant - - - - - - DISTANCE=81 rs5904816 X:147026266 T 2332 NM_001185081.1 Transcript intron_variant - - - - - - rs5904816 X:147026266 T ENSESTG00000004041 ENSESTT00000010224 Transcript downstream_gene_variant - - - - - - DISTANCE=4147 rs5904816 X:147026266 T ENSESTG00000004041 ENSESTT00000010266 Transcript upstream_gene_variant - - - - - - DISTANCE=795 rs5904816 X:147026266 T ENSESTG00000004041 ENSESTT00000010230 Transcript downstream_gene_variant - - - - - - DISTANCE=4147 rs5904816 X:147026266 T CCDS55519.1 CCDS55519.1 Transcript intron_variant - - - - - - rs5904816 X:147026266 T 2332 NM_002024.5 Transcript intron_variant - - - - - - rs5904816 X:147026266 T ENSESTG00000004041 ENSESTT00000010241 Transcript intron_variant - - - - - - rs5904816 X:147026266 T ENSESTG00000004041 ENSESTT00000010262 Transcript upstream_gene_variant - - - - - - DISTANCE=88 rs5904816 X:147026266 T 2332 NM_001185075.1 Transcript intron_variant - - - - - - rs5904816 X:147026266 T CCDS14682.1 CCDS14682.1 Transcript intron_variant - - - - - - rs5904816 X:147026266 T CCDS55518.1 CCDS55518.1 Transcript intron_variant - - - - - - rs5904816 X:147026266 T 2332 NR_033700.1 Transcript intron_variant,nc_transcript_variant - - - - - - rs5951864 X:147059478 T ENSESTG00000004077 ENSESTT00000010290 Transcript upstream_gene_variant - - - - - - DISTANCE=3381 rs5951864 X:147059478 T ENSESTG00000004077 ENSESTT00000010289 Transcript upstream_gene_variant - - - - - - DISTANCE=3381 rs5951864 X:147059478 T 158521 NM_152578.2 Transcript upstream_gene_variant - - - - - - DISTANCE=3371 rs5951864 X:147059478 T CCDS14683.1 CCDS14683.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3445 rs5951864 X:147059478 T ENSESTG00000004077 ENSESTT00000010288 Transcript upstream_gene_variant - - - - - - DISTANCE=3381 rs5904655 X:147065627 T ENSESTG00000004077 ENSESTT00000010290 Transcript intron_variant - - - - - - rs5904655 X:147065627 T ENSESTG00000004077 ENSESTT00000010289 Transcript intron_variant - - - - - - rs5904655 X:147065627 T 158521 NM_152578.2 Transcript intron_variant - - - - - - rs5904655 X:147065627 T CCDS14683.1 CCDS14683.1 Transcript intron_variant - - - - - - rs5904655 X:147065627 T ENSESTG00000004077 ENSESTT00000010288 Transcript intron_variant - - - - - - rs5904824 X:147065958 T ENSESTG00000004077 ENSESTT00000010290 Transcript intron_variant - - - - - - rs5904824 X:147065958 T ENSESTG00000004077 ENSESTT00000010289 Transcript intron_variant - - - - - - rs5904824 X:147065958 T 158521 NM_152578.2 Transcript intron_variant - - - - - - rs5904824 X:147065958 T CCDS14683.1 CCDS14683.1 Transcript intron_variant - - - - - - rs5904824 X:147065958 T ENSESTG00000004077 ENSESTT00000010288 Transcript intron_variant - - - - - - rs5951865 X:147091657 T ENSESTG00000004077 ENSESTT00000010289 Transcript intron_variant - - - - - - rs5951865 X:147091657 T 158521 NM_152578.2 Transcript intron_variant - - - - - - rs5951865 X:147091657 T CCDS14683.1 CCDS14683.1 Transcript intron_variant - - - - - - rs5951865 X:147091657 T ENSESTG00000004077 ENSESTT00000010288 Transcript intron_variant - - - - - - rs5951866 X:147092011 C ENSESTG00000004077 ENSESTT00000010289 Transcript intron_variant - - - - - - rs5951866 X:147092011 C 158521 NM_152578.2 Transcript intron_variant - - - - - - rs5951866 X:147092011 C CCDS14683.1 CCDS14683.1 Transcript intron_variant - - - - - - rs5951866 X:147092011 C ENSESTG00000004077 ENSESTT00000010288 Transcript intron_variant - - - - - - rs2187600 X:147100985 G ENSESTG00000004077 ENSESTT00000010289 Transcript intron_variant - - - - - - rs2187600 X:147100985 G 158521 NM_152578.2 Transcript intron_variant - - - - - - rs2187600 X:147100985 G CCDS14683.1 CCDS14683.1 Transcript intron_variant - - - - - - rs2187600 X:147100985 G ENSESTG00000004077 ENSESTT00000010288 Transcript intron_variant - - - - - - rs215110 X:147106677 A ENSESTG00000004077 ENSESTT00000010289 Transcript intron_variant - - - - - - rs215110 X:147106677 A 158521 NM_152578.2 Transcript intron_variant - - - - - - rs215110 X:147106677 A CCDS14683.1 CCDS14683.1 Transcript downstream_gene_variant - - - - - - DISTANCE=157 rs215110 X:147106677 A ENSESTG00000004077 ENSESTT00000010288 Transcript intron_variant - - - - - - rs215120 X:147136933 T ENSESTG00000004108 ENSESTT00000010373 Transcript upstream_gene_variant - - - - - - DISTANCE=2675 rs215120 X:147136933 T ENSESTG00000004108 ENSESTT00000010371 Transcript upstream_gene_variant - - - - - - DISTANCE=2675 rs215120 X:147136933 T ENSESTG00000004108 ENSESTT00000010366 Transcript upstream_gene_variant - - - - - - DISTANCE=2674 rs215120 X:147136933 T ENSESTG00000004108 ENSESTT00000010365 Transcript upstream_gene_variant - - - - - - DISTANCE=2673 rs215120 X:147136933 T ENSESTG00000004108 ENSESTT00000010356 Transcript intron_variant - - - - - - rs215121 X:147139787 T ENSESTG00000004108 ENSESTT00000010356 Transcript intron_variant - - - - - - rs5980358 X:147274782 A ENSESTG00000004088 ENSESTT00000010318 Transcript downstream_gene_variant - - - - - - DISTANCE=4753 rs5980358 X:147274782 A ENSESTG00000004088 ENSESTT00000010345 Transcript downstream_gene_variant - - - - - - DISTANCE=4908 rs5980358 X:147274782 A ENSESTG00000004088 ENSESTT00000010338 Transcript downstream_gene_variant - - - - - - DISTANCE=4729 rs5936371 X:147286842 T - - - intergenic_variant - - - - - - rs5936375 X:147530368 C - - - intergenic_variant - - - - - - rs5936378 X:147550884 A - - - intergenic_variant - - - - - - rs5980536 X:147566842 A - - - intergenic_variant - - - - - - rs10218049 X:147572309 T - - - intergenic_variant - - - - - - rs5936210 X:147572397 C - - - intergenic_variant - - - - - - rs4844063 X:147654137 A ENSESTG00000000428 ENSESTT00000001063 Transcript intron_variant - - - - - - rs4844063 X:147654137 A 2334 NM_001169124.1 Transcript intron_variant - - - - - - rs4844063 X:147654137 A CCDS55520.1 CCDS55520.1 Transcript intron_variant - - - - - - rs4844063 X:147654137 A 2334 NM_001169123.1 Transcript intron_variant - - - - - - rs4844063 X:147654137 A 2334 NM_001169122.1 Transcript intron_variant - - - - - - rs4844063 X:147654137 A 2334 NM_002025.3 Transcript intron_variant - - - - - - rs4844063 X:147654137 A 2334 NM_001169125.1 Transcript intron_variant - - - - - - rs4844063 X:147654137 A CCDS14684.1 CCDS14684.1 Transcript intron_variant - - - - - - rs2880490 X:147705626 T ENSESTG00000000428 ENSESTT00000001063 Transcript intron_variant - - - - - - rs2880490 X:147705626 T 2334 NM_001169124.1 Transcript intron_variant - - - - - - rs2880490 X:147705626 T CCDS55520.1 CCDS55520.1 Transcript intron_variant - - - - - - rs2880490 X:147705626 T 2334 NM_001169123.1 Transcript intron_variant - - - - - - rs2880490 X:147705626 T 2334 NM_001169122.1 Transcript intron_variant - - - - - - rs2880490 X:147705626 T 2334 NM_002025.3 Transcript intron_variant - - - - - - rs2880490 X:147705626 T ENSESTG00000000430 ENSESTT00000001068 Transcript upstream_gene_variant - - - - - - DISTANCE=1333 rs2880490 X:147705626 T 2334 NM_001169125.1 Transcript intron_variant - - - - - - rs2880490 X:147705626 T CCDS14684.1 CCDS14684.1 Transcript intron_variant - - - - - - rs5980378 X:147726473 A ENSESTG00000000428 ENSESTT00000001063 Transcript intron_variant - - - - - - rs5980378 X:147726473 A 2334 NM_001169124.1 Transcript intron_variant - - - - - - rs5980378 X:147726473 A CCDS55520.1 CCDS55520.1 Transcript intron_variant - - - - - - rs5980378 X:147726473 A 2334 NM_001169123.1 Transcript intron_variant - - - - - - rs5980378 X:147726473 A 2334 NM_001169122.1 Transcript intron_variant - - - - - - rs5980378 X:147726473 A 2334 NM_002025.3 Transcript intron_variant - - - - - - rs5980378 X:147726473 A 2334 NM_001169125.1 Transcript intron_variant - - - - - - rs5980378 X:147726473 A CCDS14684.1 CCDS14684.1 Transcript intron_variant - - - - - - rs241112 X:147746208 C ENSESTG00000000428 ENSESTT00000001063 Transcript downstream_gene_variant - - - - - - DISTANCE=2344 rs241112 X:147746208 C 2334 NM_001169124.1 Transcript intron_variant - - - - - - rs241112 X:147746208 C CCDS55520.1 CCDS55520.1 Transcript intron_variant - - - - - - rs241112 X:147746208 C 2334 NM_001169123.1 Transcript intron_variant - - - - - - rs241112 X:147746208 C 2334 NM_001169122.1 Transcript intron_variant - - - - - - rs241112 X:147746208 C 2334 NM_002025.3 Transcript intron_variant - - - - - - rs241112 X:147746208 C 2334 NM_001169125.1 Transcript intron_variant - - - - - - rs241112 X:147746208 C CCDS14684.1 CCDS14684.1 Transcript intron_variant - - - - - - rs241112 X:147746208 C ENSESTG00000000435 ENSESTT00000001077 Transcript intron_variant - - - - - - rs1265389 X:147880873 C ENSESTG00000000435 ENSESTT00000001084 Transcript intron_variant - - - - - - rs1265389 X:147880873 C 2334 NM_001169124.1 Transcript intron_variant - - - - - - rs1265389 X:147880873 C CCDS55520.1 CCDS55520.1 Transcript intron_variant - - - - - - rs1265389 X:147880873 C 2334 NM_001169123.1 Transcript intron_variant - - - - - - rs1265389 X:147880873 C 2334 NM_001169122.1 Transcript intron_variant - - - - - - rs1265389 X:147880873 C CCDS55521.1 CCDS55521.1 Transcript intron_variant - - - - - - rs1265389 X:147880873 C 2334 NM_002025.3 Transcript intron_variant - - - - - - rs1265389 X:147880873 C 2334 NM_001170628.1 Transcript intron_variant - - - - - - rs1265389 X:147880873 C 2334 NM_001169125.1 Transcript intron_variant - - - - - - rs1265389 X:147880873 C ENSESTG00000000435 ENSESTT00000001081 Transcript intron_variant - - - - - - rs1265389 X:147880873 C CCDS14684.1 CCDS14684.1 Transcript intron_variant - - - - - - rs1265389 X:147880873 C ENSESTG00000000435 ENSESTT00000001077 Transcript intron_variant - - - - - - rs137901308 X:147993959 C ENSESTG00000000435 ENSESTT00000001084 Transcript intron_variant - - - - - - rs137901308 X:147993959 C 2334 NM_001169124.1 Transcript intron_variant - - - - - - rs137901308 X:147993959 C CCDS55520.1 CCDS55520.1 Transcript intron_variant - - - - - - rs137901308 X:147993959 C 2334 NM_001169123.1 Transcript intron_variant - - - - - - rs137901308 X:147993959 C 2334 NM_001169122.1 Transcript intron_variant - - - - - - rs137901308 X:147993959 C CCDS55521.1 CCDS55521.1 Transcript intron_variant - - - - - - rs137901308 X:147993959 C 2334 NM_002025.3 Transcript intron_variant - - - - - - rs137901308 X:147993959 C 2334 NM_001170628.1 Transcript intron_variant - - - - - - rs137901308 X:147993959 C 2334 NM_001169125.1 Transcript intron_variant - - - - - - rs137901308 X:147993959 C ENSESTG00000000435 ENSESTT00000001081 Transcript intron_variant - - - - - - rs137901308 X:147993959 C CCDS14684.1 CCDS14684.1 Transcript intron_variant - - - - - - rs137901308 X:147993959 C ENSESTG00000000435 ENSESTT00000001077 Transcript intron_variant - - - - - - rs185059120 X:148009315 A ENSESTG00000000435 ENSESTT00000001084 Transcript intron_variant - - - - - - rs185059120 X:148009315 A 2334 NM_001169124.1 Transcript intron_variant - - - - - - rs185059120 X:148009315 A CCDS55520.1 CCDS55520.1 Transcript intron_variant - - - - - - rs185059120 X:148009315 A 2334 NM_001169123.1 Transcript intron_variant - - - - - - rs185059120 X:148009315 A 2334 NM_001169122.1 Transcript intron_variant - - - - - - rs185059120 X:148009315 A CCDS55521.1 CCDS55521.1 Transcript intron_variant - - - - - - rs185059120 X:148009315 A 2334 NM_002025.3 Transcript intron_variant - - - - - - rs185059120 X:148009315 A 2334 NM_001170628.1 Transcript intron_variant - - - - - - rs185059120 X:148009315 A 2334 NM_001169125.1 Transcript intron_variant - - - - - - rs185059120 X:148009315 A ENSESTG00000000435 ENSESTT00000001081 Transcript intron_variant - - - - - - rs185059120 X:148009315 A CCDS14684.1 CCDS14684.1 Transcript intron_variant - - - - - - rs185059120 X:148009315 A ENSESTG00000000435 ENSESTT00000001077 Transcript intron_variant - - - - - - rs142788003 X:148047383 C 2334 NM_001169124.1 Transcript intron_variant - - - - - - rs142788003 X:148047383 C ENSESTG00000000443 ENSESTT00000001097 Transcript upstream_gene_variant - - - - - - DISTANCE=1148 rs142788003 X:148047383 C ENSESTG00000000442 ENSESTT00000001085 Transcript downstream_gene_variant - - - - - - DISTANCE=3114 rs142788003 X:148047383 C CCDS55520.1 CCDS55520.1 Transcript intron_variant - - - - - - rs142788003 X:148047383 C 2334 NM_001169123.1 Transcript intron_variant - - - - - - rs142788003 X:148047383 C 2334 NM_001169122.1 Transcript intron_variant - - - - - - rs142788003 X:148047383 C CCDS55521.1 CCDS55521.1 Transcript intron_variant - - - - - - rs142788003 X:148047383 C 2334 NM_002025.3 Transcript intron_variant - - - - - - rs142788003 X:148047383 C 2334 NM_001170628.1 Transcript intron_variant - - - - - - rs142788003 X:148047383 C 2334 NM_001169125.1 Transcript intron_variant - - - - - - rs142788003 X:148047383 C CCDS14684.1 CCDS14684.1 Transcript intron_variant - - - - - - rs190603991 X:148064633 G 2334 NM_001169124.1 Transcript intron_variant - - - - - - rs190603991 X:148064633 G ENSESTG00000000443 ENSESTT00000001097 Transcript downstream_gene_variant - - - - - - DISTANCE=4714 rs190603991 X:148064633 G CCDS55520.1 CCDS55520.1 Transcript intron_variant - - - - - - rs190603991 X:148064633 G ENSESTG00000000447 ENSESTT00000001104 Transcript intron_variant - - - - - - rs190603991 X:148064633 G 2334 NM_001169123.1 Transcript intron_variant - - - - - - rs190603991 X:148064633 G 2334 NM_001169122.1 Transcript intron_variant - - - - - - rs190603991 X:148064633 G ENSESTG00000000447 ENSESTT00000001112 Transcript intron_variant - - - - - - rs190603991 X:148064633 G CCDS55521.1 CCDS55521.1 Transcript intron_variant - - - - - - rs190603991 X:148064633 G 2334 NM_002025.3 Transcript intron_variant - - - - - - rs190603991 X:148064633 G 2334 NM_001170628.1 Transcript intron_variant - - - - - - rs190603991 X:148064633 G 2334 NM_001169125.1 Transcript intron_variant - - - - - - rs190603991 X:148064633 G CCDS14684.1 CCDS14684.1 Transcript intron_variant - - - - - - rs141776682 X:148081451 G 2334 NM_001169124.1 Transcript 3_prime_UTR_variant 12899 - - - - - rs141776682 X:148081451 G 2334 NM_001170628.1 Transcript 3_prime_UTR_variant 11538 - - - - - rs141776682 X:148081451 G 2334 NM_001169125.1 Transcript 3_prime_UTR_variant 12887 - - - - - rs141776682 X:148081451 G 2334 NM_001169123.1 Transcript 3_prime_UTR_variant 12974 - - - - - rs141776682 X:148081451 G 2334 NM_001169122.1 Transcript 3_prime_UTR_variant 12899 - - - - - rs141776682 X:148081451 G 2334 NM_002025.3 Transcript 3_prime_UTR_variant 13004 - - - - - rs140427496 X:148186943 C - - - intergenic_variant - - - - - - rs193203623 X:148393642 C - - - intergenic_variant - - - - - - rs184052107 X:148726950 G ENSESTG00000033340 ENSESTT00000084192 Transcript intron_variant - - - - - - rs5925416 X:149497600 C - - - intergenic_variant - - - - - - rs6627341 X:149523009 T - - - intergenic_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039767 Transcript intron_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039781 Transcript intron_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039733 Transcript intron_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039776 Transcript intron_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039753 Transcript intron_variant - - - - - - rs621458 X:149597176 C 10046 NM_001177465.1 Transcript intron_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039747 Transcript intron_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039719 Transcript intron_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039724 Transcript intron_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039783 Transcript intron_variant - - - - - - rs621458 X:149597176 C ENSESTG00000015833 ENSESTT00000039754 Transcript intron_variant - - - - - - rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039733 Transcript intron_variant - - - - - - rs6526056 X:149613493 T CCDS55526.1 CCDS55526.1 Transcript upstream_gene_variant - - - - - - DISTANCE=290 rs6526056 X:149613493 T 10046 NM_001177465.1 Transcript intron_variant - - - - - - rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039719 Transcript intron_variant - - - - - - rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039724 Transcript intron_variant - - - - - - rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039767 Transcript intron_variant - - - - - - rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039781 Transcript intron_variant - - - - - - rs6526056 X:149613493 T 10046 NM_005491.3 Transcript upstream_gene_variant - - - - - - DISTANCE=227 rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039753 Transcript intron_variant - - - - - - rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039776 Transcript intron_variant - - - - - - rs6526056 X:149613493 T 10046 NM_001177466.1 Transcript upstream_gene_variant - - - - - - DISTANCE=227 rs6526056 X:149613493 T CCDS14693.2 CCDS14693.2 Transcript upstream_gene_variant - - - - - - DISTANCE=290 rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039747 Transcript intron_variant - - - - - - rs6526056 X:149613493 T CCDS55525.1 CCDS55525.1 Transcript upstream_gene_variant - - - - - - DISTANCE=290 rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039754 Transcript intron_variant - - - - - - rs6526056 X:149613493 T ENSESTG00000015833 ENSESTT00000039783 Transcript intron_variant - - - - - - rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039733 Transcript intron_variant - - - - - - rs6526057 X:149613617 C CCDS55526.1 CCDS55526.1 Transcript upstream_gene_variant - - - - - - DISTANCE=166 rs6526057 X:149613617 C 10046 NM_001177465.1 Transcript intron_variant - - - - - - rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039719 Transcript intron_variant - - - - - - rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039724 Transcript intron_variant - - - - - - rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039767 Transcript intron_variant - - - - - - rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039781 Transcript intron_variant - - - - - - rs6526057 X:149613617 C 10046 NM_005491.3 Transcript upstream_gene_variant - - - - - - DISTANCE=103 rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039753 Transcript intron_variant - - - - - - rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039776 Transcript intron_variant - - - - - - rs6526057 X:149613617 C 10046 NM_001177466.1 Transcript upstream_gene_variant - - - - - - DISTANCE=103 rs6526057 X:149613617 C CCDS14693.2 CCDS14693.2 Transcript upstream_gene_variant - - - - - - DISTANCE=166 rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039747 Transcript intron_variant - - - - - - rs6526057 X:149613617 C CCDS55525.1 CCDS55525.1 Transcript upstream_gene_variant - - - - - - DISTANCE=166 rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039754 Transcript intron_variant - - - - - - rs6526057 X:149613617 C ENSESTG00000015833 ENSESTT00000039783 Transcript intron_variant - - - - - - rs6526082 X:149641802 G 10046 NM_005491.3 Transcript intron_variant - - - - - - rs6526082 X:149641802 G ENSESTG00000015833 ENSESTT00000039781 Transcript intron_variant - - - - - - rs6526082 X:149641802 G ENSESTG00000015833 ENSESTT00000039733 Transcript intron_variant - - - - - - rs6526082 X:149641802 G ENSESTG00000015833 ENSESTT00000039776 Transcript intron_variant - - - - - - rs6526082 X:149641802 G ENSESTG00000015833 ENSESTT00000039753 Transcript intron_variant - - - - - - rs6526082 X:149641802 G 10046 NM_001177466.1 Transcript intron_variant - - - - - - rs6526082 X:149641802 G CCDS55526.1 CCDS55526.1 Transcript intron_variant - - - - - - rs6526082 X:149641802 G CCDS14693.2 CCDS14693.2 Transcript intron_variant - - - - - - rs6526082 X:149641802 G 10046 NM_001177465.1 Transcript intron_variant - - - - - - rs6526082 X:149641802 G CCDS55525.1 CCDS55525.1 Transcript intron_variant - - - - - - rs6526082 X:149641802 G ENSESTG00000015833 ENSESTT00000039747 Transcript intron_variant - - - - - - rs6526082 X:149641802 G ENSESTG00000015833 ENSESTT00000039719 Transcript intron_variant - - - - - - rs6526082 X:149641802 G ENSESTG00000015833 ENSESTT00000039724 Transcript intron_variant - - - - - - rs6526082 X:149641802 G ENSESTG00000015833 ENSESTT00000039783 Transcript intron_variant - - - - - - rs6526082 X:149641802 G ENSESTG00000015833 ENSESTT00000039754 Transcript intron_variant - - - - - - rs222352 X:149884781 A 8776 NM_003828.2 Transcript intron_variant - - - - - - rs222352 X:149884781 A ENSESTG00000015934 ENSESTT00000040059 Transcript intron_variant - - - - - - rs222352 X:149884781 A ENSESTG00000015934 ENSESTT00000040043 Transcript intron_variant - - - - - - rs222352 X:149884781 A CCDS14695.1 CCDS14695.1 Transcript intron_variant - - - - - - rs222352 X:149884781 A ENSESTG00000015934 ENSESTT00000040047 Transcript intron_variant - - - - - - rs222352 X:149884781 A ENSESTG00000015934 ENSESTT00000040029 Transcript intron_variant - - - - - - rs222352 X:149884781 A ENSESTG00000015934 ENSESTT00000040053 Transcript intron_variant - - - - - - rs222351 X:149884792 G 8776 NM_003828.2 Transcript intron_variant - - - - - - rs222351 X:149884792 G ENSESTG00000015934 ENSESTT00000040059 Transcript intron_variant - - - - - - rs222351 X:149884792 G ENSESTG00000015934 ENSESTT00000040043 Transcript intron_variant - - - - - - rs222351 X:149884792 G CCDS14695.1 CCDS14695.1 Transcript intron_variant - - - - - - rs222351 X:149884792 G ENSESTG00000015934 ENSESTT00000040047 Transcript intron_variant - - - - - - rs222351 X:149884792 G ENSESTG00000015934 ENSESTT00000040029 Transcript intron_variant - - - - - - rs222351 X:149884792 G ENSESTG00000015934 ENSESTT00000040053 Transcript intron_variant - - - - - - rs5970475 X:149946638 G CCDS55527.1 CCDS55527.1 Transcript intron_variant - - - - - - rs5970475 X:149946638 G 83692 NM_134446.3 Transcript intron_variant - - - - - - rs5970475 X:149946638 G ENSESTG00000016000 ENSESTT00000040105 Transcript intron_variant - - - - - - rs5970475 X:149946638 G ENSESTG00000016000 ENSESTT00000040122 Transcript intron_variant - - - - - - rs5970475 X:149946638 G ENSESTG00000016034 ENSESTT00000040356 Transcript intron_variant - - - - - - rs5970475 X:149946638 G ENSESTG00000016034 ENSESTT00000040330 Transcript intron_variant - - - - - - rs5970475 X:149946638 G ENSESTG00000016034 ENSESTT00000040316 Transcript intron_variant - - - - - - rs5970475 X:149946638 G CCDS14697.1 CCDS14697.1 Transcript intron_variant - - - - - - rs5970475 X:149946638 G 83692 NM_001242614.1 Transcript intron_variant - - - - - - rs5970475 X:149946638 G CCDS35427.1 CCDS35427.1 Transcript intron_variant - - - - - - rs5970475 X:149946638 G 83692 NM_031462.3 Transcript intron_variant - - - - - - rs5970475 X:149946638 G 83692 NM_134445.3 Transcript intron_variant - - - - - - rs5970475 X:149946638 G 83692 NM_001184808.1 Transcript intron_variant - - - - - - rs5970475 X:149946638 G ENSESTG00000016034 ENSESTT00000040209 Transcript intron_variant - - - - - - rs5970475 X:149946638 G CCDS14698.1 CCDS14698.1 Transcript intron_variant - - - - - - rs417765 X:150124197 T - - - intergenic_variant - - - - - - rs56393835 X:150189750 C - - - intergenic_variant - - - - - - rs4828796 X:150234816 G - - - intergenic_variant - - - - - - rs5925508 X:150250845 G - ENSR00000161456 RegulatoryFeature regulatory_region_variant - - - - - - rs5925508 X:150250845 G - - - intergenic_variant - - - - - - rs6418519 X:150266846 C - - - intergenic_variant - - - - - - rs647033 X:150337404 G 100422930 NR_036256.1 Transcript downstream_gene_variant - - - - - - DISTANCE=606 rs482961 X:150350922 T 9248 NM_004224.3 Transcript downstream_gene_variant - - - - - - DISTANCE=985 rs482961 X:150350922 T ENSESTG00000033899 ENSESTT00000085678 Transcript upstream_gene_variant - - - - - - DISTANCE=4614 rs482961 X:150350922 T CCDS44012.1 CCDS44012.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1013 rs482961 X:150350922 T ENSESTG00000033795 ENSESTT00000085440 Transcript downstream_gene_variant - - - - - - DISTANCE=2312 rs1149366 X:150412612 T - - - intergenic_variant - - - - - - rs1202947 X:150420183 T - - - intergenic_variant - - - - - - rs5924910 X:150515438 G - - - intergenic_variant - - - - - - rs5924626 X:150521200 G - - - intergenic_variant - - - - - - rs176450 X:150564421 C ENSESTG00000033802 ENSESTT00000085458 Transcript upstream_gene_variant - - - - - - DISTANCE=599 rs176450 X:150564421 C CCDS35430.1 CCDS35430.1 Transcript upstream_gene_variant - - - - - - DISTANCE=1360 rs176450 X:150564421 C ENSESTG00000033802 ENSESTT00000085474 Transcript upstream_gene_variant - - - - - - DISTANCE=1306 rs176450 X:150564421 C 203547 NM_001017980.3 Transcript upstream_gene_variant - - - - - - DISTANCE=1236 rs176450 X:150564421 C ENSESTG00000033802 ENSESTT00000085463 Transcript upstream_gene_variant - - - - - - DISTANCE=840 rs3859912 X:150807477 A CCDS35431.1 CCDS35431.1 Transcript intron_variant - - - - - - rs3859912 X:150807477 A ENSESTG00000033815 ENSESTT00000085520 Transcript intron_variant - - - - - - rs3859912 X:150807477 A 139135 NM_173493.2 Transcript intron_variant - - - - - - rs5969823 X:150935394 G - - - intergenic_variant - - - - - - rs6627495 X:151102402 T - - - intergenic_variant - - - - - - rs2472362 X:151183743 G - - - intergenic_variant - - - - - - rs4828693 X:151413619 G - ENSR00000483010 RegulatoryFeature regulatory_region_variant - - - - - - rs4828693 X:151413619 G ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs4828693 X:151413619 G ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs4828693 X:151413619 G ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs4828693 X:151413619 G ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs4828693 X:151413619 G ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs4828693 X:151413619 G 2556 NM_000808.3 Transcript intron_variant - - - - - - rs4828693 X:151413619 G CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs4828693 X:151413619 G ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs4828693 X:151413619 G ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs4828693 X:151413619 G ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs4370681 X:151434690 G ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs4370681 X:151434690 G ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs4370681 X:151434690 G ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs4370681 X:151434690 G ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs4370681 X:151434690 G ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs4370681 X:151434690 G 2556 NM_000808.3 Transcript intron_variant - - - - - - rs4370681 X:151434690 G CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs4370681 X:151434690 G ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs4370681 X:151434690 G ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs4370681 X:151434690 G ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs4431735 X:151451709 G ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs4431735 X:151451709 G ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs4431735 X:151451709 G ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs4431735 X:151451709 G ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs4431735 X:151451709 G ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs4431735 X:151451709 G 2556 NM_000808.3 Transcript intron_variant - - - - - - rs4431735 X:151451709 G CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs4431735 X:151451709 G ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs4431735 X:151451709 G ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs4431735 X:151451709 G ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs5925154 X:151455770 C ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs5925154 X:151455770 C ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs5925154 X:151455770 C ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs5925154 X:151455770 C ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs5925154 X:151455770 C ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs5925154 X:151455770 C 2556 NM_000808.3 Transcript intron_variant - - - - - - rs5925154 X:151455770 C CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs5925154 X:151455770 C ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs5925154 X:151455770 C ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs5925154 X:151455770 C ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs5925157 X:151467684 A ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs5925157 X:151467684 A ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs5925157 X:151467684 A ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs5925157 X:151467684 A ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs5925157 X:151467684 A ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs5925157 X:151467684 A 2556 NM_000808.3 Transcript intron_variant - - - - - - rs5925157 X:151467684 A CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs5925157 X:151467684 A ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs5925157 X:151467684 A ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs5925157 X:151467684 A ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs6627228 X:151471122 G ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs6627228 X:151471122 G ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs6627228 X:151471122 G ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs6627228 X:151471122 G ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs6627228 X:151471122 G ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs6627228 X:151471122 G 2556 NM_000808.3 Transcript intron_variant - - - - - - rs6627228 X:151471122 G CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs6627228 X:151471122 G ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs6627228 X:151471122 G ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs6627228 X:151471122 G ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs7050378 X:151484274 C ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs7050378 X:151484274 C ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs7050378 X:151484274 C ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs7050378 X:151484274 C ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs7050378 X:151484274 C ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs7050378 X:151484274 C 2556 NM_000808.3 Transcript intron_variant - - - - - - rs7050378 X:151484274 C CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs7050378 X:151484274 C ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs7050378 X:151484274 C ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs7050378 X:151484274 C ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs5970271 X:151484590 C ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs5970271 X:151484590 C ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs5970271 X:151484590 C ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs5970271 X:151484590 C ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs5970271 X:151484590 C ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs5970271 X:151484590 C 2556 NM_000808.3 Transcript intron_variant - - - - - - rs5970271 X:151484590 C CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs5970271 X:151484590 C ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs5970271 X:151484590 C ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs5970271 X:151484590 C ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs4828587 X:151490046 G ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs4828587 X:151490046 G ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs4828587 X:151490046 G ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs4828587 X:151490046 G ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs4828587 X:151490046 G ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs4828587 X:151490046 G 2556 NM_000808.3 Transcript intron_variant - - - - - - rs4828587 X:151490046 G CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs4828587 X:151490046 G ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs4828587 X:151490046 G ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs4828587 X:151490046 G ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs5925160 X:151491107 G ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs5925160 X:151491107 G ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs5925160 X:151491107 G ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs5925160 X:151491107 G ENSESTG00000019355 ENSESTT00000048786 Transcript intron_variant - - - - - - rs5925160 X:151491107 G ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs5925160 X:151491107 G 2556 NM_000808.3 Transcript intron_variant - - - - - - rs5925160 X:151491107 G CCDS14706.1 CCDS14706.1 Transcript intron_variant - - - - - - rs5925160 X:151491107 G ENSESTG00000019355 ENSESTT00000048789 Transcript intron_variant - - - - - - rs5925160 X:151491107 G ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs5925160 X:151491107 G ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs5970295 X:151573687 G ENSESTG00000019355 ENSESTT00000048777 Transcript intron_variant - - - - - - rs5970295 X:151573687 G ENSESTG00000019355 ENSESTT00000048760 Transcript intron_variant - - - - - - rs5970295 X:151573687 G ENSESTG00000019355 ENSESTT00000048743 Transcript intron_variant - - - - - - rs5970295 X:151573687 G ENSESTG00000019355 ENSESTT00000048734 Transcript intron_variant - - - - - - rs5970295 X:151573687 G ENSESTG00000019355 ENSESTT00000048768 Transcript intron_variant - - - - - - rs5970295 X:151573687 G ENSESTG00000019355 ENSESTT00000048753 Transcript intron_variant - - - - - - rs5970295 X:151573687 G 2556 NM_000808.3 Transcript intron_variant - - - - - - rs12387404 X:151702740 T - - - intergenic_variant - - - - - - rs1016866 X:151720608 G - - - intergenic_variant - - - - - - rs5924765 X:152033544 G ENSESTG00000018899 ENSESTT00000047781 Transcript intron_variant - - - - - - rs5924765 X:152033544 G 50814 NM_015922.2 Transcript intron_variant - - - - - - rs5924765 X:152033544 G CCDS14717.1 CCDS14717.1 Transcript intron_variant - - - - - - rs5924765 X:152033544 G ENSESTG00000018899 ENSESTT00000047744 Transcript intron_variant - - - - - - rs5924765 X:152033544 G ENSESTG00000018899 ENSESTT00000047760 Transcript downstream_gene_variant - - - - - - DISTANCE=2351 rs5924765 X:152033544 G ENSESTG00000018899 ENSESTT00000047730 Transcript intron_variant - - - - - - rs5924765 X:152033544 G 50814 NM_001129765.1 Transcript intron_variant - - - - - - rs6627279 X:152073421 C - ENSR00000073852 RegulatoryFeature regulatory_region_variant - - - - - - rs6627279 X:152073421 C - - - intergenic_variant - - - - - - rs4007728 X:152078174 C CCDS55530.1 CCDS55530.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4860 rs4007728 X:152078174 C CCDS55531.1 CCDS55531.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4860 rs4007728 X:152078174 C 7739 NM_001178108.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4812 rs4007728 X:152078174 C 7739 NM_007150.3 Transcript upstream_gene_variant - - - - - - DISTANCE=4812 rs4007728 X:152078174 C 7739 NM_001178107.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4812 rs4007728 X:152078174 C 7739 NM_001178109.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4812 rs4007728 X:152078174 C 7739 NM_001178110.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4812 rs4007728 X:152078174 C CCDS55528.1 CCDS55528.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4860 rs4007728 X:152078174 C 7739 NM_001178106.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4812 rs4007728 X:152078174 C CCDS48184.1 CCDS48184.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4860 rs4007728 X:152078174 C CCDS55529.1 CCDS55529.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4860 rs5925251 X:152080129 G CCDS55530.1 CCDS55530.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2905 rs5925251 X:152080129 G CCDS55531.1 CCDS55531.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2905 rs5925251 X:152080129 G 7739 NM_001178108.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2857 rs5925251 X:152080129 G 7739 NM_007150.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2857 rs5925251 X:152080129 G 7739 NM_001178107.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2857 rs5925251 X:152080129 G 7739 NM_001178109.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2857 rs5925251 X:152080129 G 7739 NM_001178110.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2857 rs5925251 X:152080129 G CCDS55528.1 CCDS55528.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2905 rs5925251 X:152080129 G 7739 NM_001178106.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2857 rs5925251 X:152080129 G CCDS48184.1 CCDS48184.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2905 rs5925251 X:152080129 G CCDS55529.1 CCDS55529.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2905 rs5925257 X:152095257 G - ENSR00000483038 RegulatoryFeature regulatory_region_variant - - - - - - rs5925257 X:152095257 G CCDS55530.1 CCDS55530.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G CCDS55531.1 CCDS55531.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G 7739 NM_001178108.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G 7739 NM_007150.3 Transcript intron_variant - - - - - - rs5925257 X:152095257 G CCDS55532.1 CCDS55532.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G 7739 NM_001178107.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G 7739 NM_001178109.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G 7739 NM_001178110.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G 7739 NM_001178113.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G CCDS55528.1 CCDS55528.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G 7739 NM_001178106.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G ENSESTG00000019013 ENSESTT00000047816 Transcript intron_variant - - - - - - rs5925257 X:152095257 G CCDS48184.1 CCDS48184.1 Transcript intron_variant - - - - - - rs5925257 X:152095257 G CCDS55529.1 CCDS55529.1 Transcript intron_variant - - - - - - rs6526145 X:152165448 C 114824 NM_001103151.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4687 rs6526145 X:152165448 C 114824 NM_001184924.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2777 rs6526145 X:152165448 C ENSESTG00000019160 ENSESTT00000048176 Transcript upstream_gene_variant - - - - - - DISTANCE=2720 rs6526145 X:152165448 C 114824 NM_001103150.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4687 rs6526145 X:152165448 C 114824 NM_052926.2 Transcript upstream_gene_variant - - - - - - DISTANCE=4687 rs67715919 X:152420408 G - - - intergenic_variant - - - - - - rs4240080 X:152568602 A - - - intergenic_variant - - - - - - rs5970449 X:152607647 T ENSESTG00000035759 ENSESTT00000090351 Transcript upstream_gene_variant - - - - - - DISTANCE=2990 rs5970449 X:152607647 T 10838 NM_001080485.3 Transcript intron_variant - - - - - - rs5970449 X:152607647 T ENSESTG00000035759 ENSESTT00000090350 Transcript intron_variant - - - - - - rs11156602 X:152669622 G 649238 XM_003846441.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3474 rs2980022 X:152707575 G - ENSR00000483067 RegulatoryFeature regulatory_region_variant - - - - - - rs2980022 X:152707575 G CCDS35437.1 CCDS35437.1 Transcript downstream_gene_variant - - - - - - DISTANCE=2603 rs2980022 X:152707575 G 11219 NM_080701.3 Transcript downstream_gene_variant - - - - - - DISTANCE=2603 rs3020971 X:152741935 A ENSESTG00000032332 ENSESTT00000081618 Transcript intron_variant - - - - - - rs4507945 X:152878700 C ENSESTG00000035765 ENSESTT00000090362 Transcript downstream_gene_variant - - - - - - DISTANCE=329 rs5986915 X:152901960 C - ENSR00000483094 RegulatoryFeature regulatory_region_variant - - - - - - rs5986915 X:152901960 C - - - intergenic_variant - - - - - - rs6643635 X:152916023 G 1852 NM_001395.2 Transcript 3_prime_UTR_variant 1622 - - - - - rs6643635 X:152916023 G ENSESTG00000035766 ENSESTT00000090364 Transcript downstream_gene_variant - - - - - - DISTANCE=2556 rs6643635 X:152916023 G ENSESTG00000035766 ENSESTT00000090363 Transcript downstream_gene_variant - - - - - - DISTANCE=2323 rs6643635 X:152916023 G CCDS14724.1 CCDS14724.1 Transcript downstream_gene_variant - - - - - - DISTANCE=263 rs6643751 X:152922767 G - - - intergenic_variant - - - - - - rs5945332 X:152925119 C - - - intergenic_variant - - - - - - rs5986921 X:152950884 G CCDS14726.1 CCDS14726.1 Transcript upstream_gene_variant - - - - - - DISTANCE=3146 rs5986921 X:152950884 G ENSESTG00000035767 ENSESTT00000090366 Transcript upstream_gene_variant - - - - - - DISTANCE=3276 rs5986921 X:152950884 G ENSESTG00000032290 ENSESTT00000081523 Transcript intron_variant - - - - - - rs5986921 X:152950884 G 6535 NM_001142806.1 Transcript upstream_gene_variant - - - - - - DISTANCE=4082 rs5986921 X:152950884 G ENSESTG00000032290 ENSESTT00000081536 Transcript intron_variant - - - - - - rs5986921 X:152950884 G ENSESTG00000032290 ENSESTT00000081497 Transcript intron_variant - - - - - - rs5986921 X:152950884 G ENSESTG00000035767 ENSESTT00000090365 Transcript upstream_gene_variant - - - - - - DISTANCE=3276 rs5986921 X:152950884 G ENSESTG00000032290 ENSESTT00000081506 Transcript intron_variant - - - - - - rs5986921 X:152950884 G 6535 NM_001142805.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2868 rs5986921 X:152950884 G 6535 NM_005629.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2868 rs5945161 X:153038516 G ENSESTG00000035770 ENSESTT00000090370 Transcript downstream_gene_variant - - - - - - DISTANCE=3209 rs5945161 X:153038516 G ENSESTG00000035771 ENSESTT00000090375 Transcript downstream_gene_variant - - - - - - DISTANCE=134 rs5945161 X:153038516 G ENSESTG00000035770 ENSESTT00000090372 Transcript downstream_gene_variant - - - - - - DISTANCE=2700 rs5945161 X:153038516 G 5365 NM_005393.2 Transcript intron_variant - - - - - - rs5945161 X:153038516 G CCDS55536.1 CCDS55536.1 Transcript intron_variant - - - - - - rs5945161 X:153038516 G ENSESTG00000035770 ENSESTT00000090374 Transcript downstream_gene_variant - - - - - - DISTANCE=2885 rs5945161 X:153038516 G 5365 NM_001163257.1 Transcript intron_variant - - - - - - rs5945161 X:153038516 G CCDS14729.1 CCDS14729.1 Transcript intron_variant - - - - - - rs1543781 X:153039615 G ENSESTG00000035770 ENSESTT00000090370 Transcript downstream_gene_variant - - - - - - DISTANCE=4308 rs1543781 X:153039615 G ENSESTG00000035771 ENSESTT00000090375 Transcript downstream_gene_variant - - - - - - DISTANCE=1233 rs1543781 X:153039615 G ENSESTG00000035770 ENSESTT00000090372 Transcript downstream_gene_variant - - - - - - DISTANCE=3799 rs1543781 X:153039615 G 5365 NM_005393.2 Transcript intron_variant - - - - - - rs1543781 X:153039615 G CCDS55536.1 CCDS55536.1 Transcript intron_variant - - - - - - rs1543781 X:153039615 G ENSESTG00000035770 ENSESTT00000090374 Transcript downstream_gene_variant - - - - - - DISTANCE=3984 rs1543781 X:153039615 G 5365 NM_001163257.1 Transcript intron_variant - - - - - - rs1543781 X:153039615 G CCDS14729.1 CCDS14729.1 Transcript intron_variant - - - - - - rs2001008 X:153086696 G 57595 NM_032512.2 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081073 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081106 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081120 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081094 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081149 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081127 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081161 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081114 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081170 Transcript intron_variant - - - - - - rs2001008 X:153086696 G CCDS14732.1 CCDS14732.1 Transcript intron_variant - - - - - - rs2001008 X:153086696 G ENSESTG00000032131 ENSESTT00000081132 Transcript intron_variant - - - - - - rs78371277 X:153134521 C ENSESTG00000032083 ENSESTT00000081017 Transcript downstream_gene_variant - - - - - - DISTANCE=3084 rs78371277 X:153134521 C 3897 NM_024003.2 Transcript intron_variant - - - - - - rs78371277 X:153134521 C ENSESTG00000032083 ENSESTT00000080956 Transcript downstream_gene_variant - - - - - - DISTANCE=3201 rs78371277 X:153134521 C ENSESTG00000032083 ENSESTT00000080990 Transcript downstream_gene_variant - - - - - - DISTANCE=1362 rs78371277 X:153134521 C CCDS14734.1 CCDS14734.1 Transcript intron_variant - - - - - - rs78371277 X:153134521 C 3897 NM_000425.3 Transcript intron_variant - - - - - - rs78371277 X:153134521 C CCDS48192.1 CCDS48192.1 Transcript intron_variant - - - - - - rs78371277 X:153134521 C 3897 NM_001143963.1 Transcript intron_variant - - - - - - rs78371277 X:153134521 C CCDS14733.1 CCDS14733.1 Transcript intron_variant - - - - - - rs78371277 X:153134521 C ENSESTG00000032083 ENSESTT00000081005 Transcript downstream_gene_variant - - - - - - DISTANCE=3883 rs28593002 X:153605061 G ENSESTG00000029416 ENSESTT00000074010 Transcript downstream_gene_variant - - - - - - DISTANCE=2807 rs28593002 X:153605061 G CCDS14745.1 CCDS14745.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2784 rs28593002 X:153605061 G ENSESTG00000029434 ENSESTT00000074138 Transcript upstream_gene_variant - - - - - - DISTANCE=2090 rs28593002 X:153605061 G 2316 NM_001110556.1 Transcript upstream_gene_variant - - - - - - DISTANCE=2055 rs28593002 X:153605061 G 2010 NM_000117.2 Transcript upstream_gene_variant - - - - - - DISTANCE=2536 rs28593002 X:153605061 G ENSESTG00000027694 ENSESTT00000069711 Transcript downstream_gene_variant - - - - - - DISTANCE=102 rs28593002 X:153605061 G 2316 NM_001456.3 Transcript upstream_gene_variant - - - - - - DISTANCE=2055 rs28593002 X:153605061 G ENSESTG00000027704 ENSESTT00000069798 Transcript upstream_gene_variant - - - - - - DISTANCE=2663 rs28593002 X:153605061 G ENSESTG00000027704 ENSESTT00000069810 Transcript upstream_gene_variant - - - - - - DISTANCE=2686 rs5945211 X:153831748 C - - - intergenic_variant - - - - - - rs1509788 X:153946883 C - ENSR00001031103 RegulatoryFeature regulatory_region_variant - - - - - - rs1509788 X:153946883 C 139716 NM_001081573.1 Transcript intron_variant - - - - - - rs1509788 X:153946883 C CCDS48198.1 CCDS48198.1 Transcript intron_variant - - - - - - rs1509788 X:153946883 C CCDS14760.1 CCDS14760.1 Transcript intron_variant - - - - - - rs1509788 X:153946883 C ENSESTG00000028901 ENSESTT00000072774 Transcript intron_variant - - - - - - rs1509788 X:153946883 C ENSESTG00000028901 ENSESTT00000072756 Transcript intron_variant - - - - - - rs1509788 X:153946883 C 139716 NM_080612.2 Transcript intron_variant - - - - - - rs1467062 X:154070167 G 2157 NM_019863.2 Transcript intron_variant - - - - - - rs1467062 X:154070167 G ENSESTG00000028751 ENSESTT00000072435 Transcript intron_variant - - - - - - rs1467062 X:154070167 G CCDS35457.1 CCDS35457.1 Transcript intron_variant - - - - - - rs1467062 X:154070167 G CCDS44026.1 CCDS44026.1 Transcript intron_variant - - - - - - rs1467062 X:154070167 G ENSESTG00000028751 ENSESTT00000072466 Transcript intron_variant - - - - - - rs1467062 X:154070167 G 2157 NM_000132.3 Transcript intron_variant - - - - - - rs572013 X:154456747 G ENSESTG00000029926 ENSESTT00000075345 Transcript missense_variant 515 352 118 M/V Atg/Gtg - PolyPhen=benign;SIFT=tolerated rs572013 X:154456747 G 7411 NM_003372.5 Transcript missense_variant 426 367 123 M/V Atg/Gtg - PolyPhen=benign;SIFT=tolerated rs572013 X:154456747 G ENSESTG00000029926 ENSESTT00000075388 Transcript missense_variant 390 367 123 M/V Atg/Gtg - PolyPhen=benign;SIFT=tolerated rs572013 X:154456747 G CCDS14765.1 CCDS14765.1 Transcript missense_variant 367 367 123 M/V Atg/Gtg - PolyPhen=benign;SIFT=tolerated rs572013 X:154456747 G ENSESTG00000030382 ENSESTT00000076463 Transcript intron_variant - - - - - - rs554196 X:154459945 C ENSESTG00000029926 ENSESTT00000075345 Transcript intron_variant - - - - - - rs554196 X:154459945 C 7411 NM_003372.5 Transcript intron_variant - - - - - - rs554196 X:154459945 C ENSESTG00000029926 ENSESTT00000075388 Transcript intron_variant - - - - - - rs554196 X:154459945 C CCDS14765.1 CCDS14765.1 Transcript intron_variant - - - - - - rs554196 X:154459945 C ENSESTG00000030382 ENSESTT00000076463 Transcript intron_variant - - - - - - rs521945 X:154478969 G - - - intergenic_variant - - - - - - rs183767858 X:154723733 G 55217 NM_001184797.1 Transcript intron_variant - - - - - - rs183767858 X:154723733 G CCDS55547.1 CCDS55547.1 Transcript intron_variant - - - - - - rs183767858 X:154723733 G CCDS14768.1 CCDS14768.1 Transcript intron_variant - - - - - - rs183767858 X:154723733 G 55217 NM_018196.3 Transcript intron_variant - - - - - - rs183767858 X:154723733 G ENSESTG00000030220 ENSESTT00000076205 Transcript intron_variant - - - - - - rs183767858 X:154723733 G ENSESTG00000030220 ENSESTT00000076178 Transcript intron_variant - - - - - - rs183767858 X:154723733 G ENSESTG00000030220 ENSESTT00000076195 Transcript intron_variant - - - - - - rs183767858 X:154723733 G 100507404 NR_039991.1 Transcript non_coding_exon_variant,nc_transcript_variant 1664 - - - - - rs700438 X:155006050 T CCDS14769.4 CCDS14769.4 Transcript downstream_gene_variant - - - - - - DISTANCE=1650 rs700438 X:155006050 T 10251 NM_005840.1 Transcript 3_prime_UTR_variant 2971 - - - - - rs700438 X:155006050 T ENSESTG00000030008 ENSESTT00000075522 Transcript downstream_gene_variant - - - - - - DISTANCE=2172 rs700438 X:155006050 T ENSESTG00000030008 ENSESTT00000075502 Transcript downstream_gene_variant - - - - - - DISTANCE=2323 rs700438 X:155006050 T ENSESTG00000030008 ENSESTT00000075532 Transcript downstream_gene_variant - - - - - - DISTANCE=1302 rs700437 X:155006982 T CCDS14769.4 CCDS14769.4 Transcript downstream_gene_variant - - - - - - DISTANCE=2582 rs700437 X:155006982 T 10251 NM_005840.1 Transcript 3_prime_UTR_variant 3903 - - - - - rs700437 X:155006982 T ENSESTG00000030008 ENSESTT00000075522 Transcript downstream_gene_variant - - - - - - DISTANCE=3104 rs700437 X:155006982 T ENSESTG00000030008 ENSESTT00000075502 Transcript downstream_gene_variant - - - - - - DISTANCE=3255 rs700437 X:155006982 T ENSESTG00000030008 ENSESTT00000075532 Transcript downstream_gene_variant - - - - - - DISTANCE=2234 rs700443 X:155008583 A CCDS14769.4 CCDS14769.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4183 rs700443 X:155008583 A 10251 NM_005840.1 Transcript 3_prime_UTR_variant 5504 - - - - - rs700443 X:155008583 A ENSESTG00000030008 ENSESTT00000075522 Transcript downstream_gene_variant - - - - - - DISTANCE=4705 rs700443 X:155008583 A ENSESTG00000030008 ENSESTT00000075502 Transcript downstream_gene_variant - - - - - - DISTANCE=4856 rs700443 X:155008583 A ENSESTG00000030008 ENSESTT00000075532 Transcript downstream_gene_variant - - - - - - DISTANCE=3835 rs700444 X:155008671 A CCDS14769.4 CCDS14769.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4271 rs700444 X:155008671 A 10251 NM_005840.1 Transcript 3_prime_UTR_variant 5592 - - - - - rs700444 X:155008671 A ENSESTG00000030008 ENSESTT00000075522 Transcript downstream_gene_variant - - - - - - DISTANCE=4793 rs700444 X:155008671 A ENSESTG00000030008 ENSESTT00000075502 Transcript downstream_gene_variant - - - - - - DISTANCE=4944 rs700444 X:155008671 A ENSESTG00000030008 ENSESTT00000075532 Transcript downstream_gene_variant - - - - - - DISTANCE=3923 rs700445 X:155009102 A CCDS14769.4 CCDS14769.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4702 rs700445 X:155009102 A 10251 NM_005840.1 Transcript 3_prime_UTR_variant 6023 - - - - - rs700445 X:155009102 A ENSESTG00000030008 ENSESTT00000075532 Transcript downstream_gene_variant - - - - - - DISTANCE=4354 rs700446 X:155009225 T CCDS14769.4 CCDS14769.4 Transcript downstream_gene_variant - - - - - - DISTANCE=4825 rs700446 X:155009225 T 10251 NM_005840.1 Transcript 3_prime_UTR_variant 6146 - - - - - rs700446 X:155009225 T ENSESTG00000030008 ENSESTT00000075532 Transcript downstream_gene_variant - - - - - - DISTANCE=4477 rs700448 X:155009829 T 10251 NM_005840.1 Transcript 3_prime_UTR_variant 6750 - - - - - rs700451 X:155010077 A 10251 NM_005840.1 Transcript 3_prime_UTR_variant 6998 - - - - - rs700452 X:155010308 A 10251 NM_005840.1 Transcript 3_prime_UTR_variant 7229 - - - - - rs700454 X:155011276 T 10251 NM_005840.1 Transcript 3_prime_UTR_variant 8197 - - - - - rs700456 X:155011472 A 10251 NM_005840.1 Transcript 3_prime_UTR_variant 8393 - - - - - rs700457 X:155012137 T 10251 NM_005840.1 Transcript downstream_gene_variant - - - - - - DISTANCE=20 rs700458 X:155012663 A 10251 NM_005840.1 Transcript downstream_gene_variant - - - - - - DISTANCE=546 rs700459 X:155012831 A 10251 NM_005840.1 Transcript downstream_gene_variant - - - - - - DISTANCE=714 rs707691 X:155013481 A 10251 NM_005840.1 Transcript downstream_gene_variant - - - - - - DISTANCE=1364 rs186774336 X:155022270 A - - - intergenic_variant - - - - - - rs2889418 X:155087648 T - ENSR00001555922 RegulatoryFeature regulatory_region_variant - - - - - - rs2889418 X:155087648 T - - - intergenic_variant - - - - - - rs5983804 X:155089346 C - - - intergenic_variant - - - - - - rs6567804 X:155178490 G - - - intergenic_variant - - - - - - rs5940626 X:155181706 T - - - intergenic_variant - - - - - - rs1973882 X:155183920 A - - - intergenic_variant - - - - - - rs5983839 X:155187394 C - - - intergenic_variant - - - - - - rs4893058 X:155189235 C - - - intergenic_variant - - - - - - rs5940637 X:155189907 A - - - intergenic_variant - - - - - - rs4893059 X:155190217 G - - - intergenic_variant - - - - - - rs2092021 X:155193964 T - ENSR00001555933 RegulatoryFeature regulatory_region_variant - - - - - - rs2092021 X:155193964 T - - - intergenic_variant - - - - - -