SRX7107225 GSM4152127 SRP228821 SRS5618412 GSM4152127 ChIP-Seq GENOMIC ChIP VCaP cells were grown in DMEM medium supplemented with 10% feta bovine serum and 1% penicillin/streptomycin antibiotics at 37 degree C temperature incubator with 5% CO2. Nuclei from approximately 10 million formaldehyde crosslinked (1%; 10min at room temperature) cells were isolated and chromatin was fragmented using sonicator (bioruptor). Lysates were cleared and protein-DNA complexes were isolated using target specific antibodies and protein-A/G magnetic beads. DNA fragments were purified and libraries were prepared accorcing to standard Illumina protocol. NextSeq 500 gds 304152127 GSM4152127 GEO Accession GSM4152127 SRX7107226 GSM4152128 SRP228821 SRS5618413 GSM4152128 ChIP-Seq GENOMIC ChIP VCaP cells were grown in DMEM medium supplemented with 10% feta bovine serum and 1% penicillin/streptomycin antibiotics at 37 degree C temperature incubator with 5% CO2. Nuclei from approximately 10 million formaldehyde crosslinked (1%; 10min at room temperature) cells were isolated and chromatin was fragmented using sonicator (bioruptor). Lysates were cleared and protein-DNA complexes were isolated using target specific antibodies and protein-A/G magnetic beads. DNA fragments were purified and libraries were prepared accorcing to standard Illumina protocol. NextSeq 500 gds 304152128 GSM4152128 GEO Accession GSM4152128 SRX7107227 GSM4152129 SRP228821 SRS5618414 GSM4152129 ChIP-Seq GENOMIC ChIP VCaP cells were grown in DMEM medium supplemented with 10% feta bovine serum and 1% penicillin/streptomycin antibiotics at 37 degree C temperature incubator with 5% CO2. Nuclei from approximately 10 million formaldehyde crosslinked (1%; 10min at room temperature) cells were isolated and chromatin was fragmented using sonicator (bioruptor). Lysates were cleared and protein-DNA complexes were isolated using target specific antibodies and protein-A/G magnetic beads. DNA fragments were purified and libraries were prepared accorcing to standard Illumina protocol. NextSeq 500 gds 304152129 GSM4152129 GEO Accession GSM4152129 SRX7107228 GSM4152130 SRP228821 SRS5618415 GSM4152130 ChIP-Seq GENOMIC ChIP VCaP cells were grown in DMEM medium supplemented with 10% feta bovine serum and 1% penicillin/streptomycin antibiotics at 37 degree C temperature incubator with 5% CO2. Nuclei from approximately 10 million formaldehyde crosslinked (1%; 10min at room temperature) cells were isolated and chromatin was fragmented using sonicator (bioruptor). Lysates were cleared and protein-DNA complexes were isolated using target specific antibodies and protein-A/G magnetic beads. DNA fragments were purified and libraries were prepared accorcing to standard Illumina protocol. NextSeq 500 gds 304152130 GSM4152130 GEO Accession GSM4152130 SRX7107229 GSM4152131 SRP228821 SRS5618416 GSM4152131 ChIP-Seq GENOMIC ChIP VCaP cells were grown in DMEM medium supplemented with 10% feta bovine serum and 1% penicillin/streptomycin antibiotics at 37 degree C temperature incubator with 5% CO2. Nuclei from approximately 10 million formaldehyde crosslinked (1%; 10min at room temperature) cells were isolated and chromatin was fragmented using sonicator (bioruptor). Lysates were cleared and protein-DNA complexes were isolated using target specific antibodies and protein-A/G magnetic beads. DNA fragments were purified and libraries were prepared accorcing to standard Illumina protocol. NextSeq 500 gds 304152131 GSM4152131 GEO Accession GSM4152131 SRX7107230 GSM4152132 SRP228821 SRS5618417 GSM4152132 ChIP-Seq GENOMIC ChIP VCaP cells were grown in DMEM medium supplemented with 10% feta bovine serum and 1% penicillin/streptomycin antibiotics at 37 degree C temperature incubator with 5% CO2. Nuclei from approximately 10 million formaldehyde crosslinked (1%; 10min at room temperature) cells were isolated and chromatin was fragmented using sonicator (bioruptor). Lysates were cleared and protein-DNA complexes were isolated using target specific antibodies and protein-A/G magnetic beads. DNA fragments were purified and libraries were prepared accorcing to standard Illumina protocol. NextSeq 500 gds 304152132 GSM4152132 GEO Accession GSM4152132 SRX7107231 GSM4152133 SRP228821 SRS5618418 GSM4152133 ChIP-Seq GENOMIC ChIP VCaP cells were grown in DMEM medium supplemented with 10% feta bovine serum and 1% penicillin/streptomycin antibiotics at 37 degree C temperature incubator with 5% CO2. Nuclei from approximately 10 million formaldehyde crosslinked (1%; 10min at room temperature) cells were isolated and chromatin was fragmented using sonicator (bioruptor). Lysates were cleared and protein-DNA complexes were isolated using target specific antibodies and protein-A/G magnetic beads. DNA fragments were purified and libraries were prepared accorcing to standard Illumina protocol. NextSeq 500 gds 304152133 GSM4152133 GEO Accession GSM4152133 SRX7107232 GSM4152134 SRP228821 SRS5618419 GSM4152134 ChIP-Seq GENOMIC ChIP VCaP cells were grown in DMEM medium supplemented with 10% feta bovine serum and 1% penicillin/streptomycin antibiotics at 37 degree C temperature incubator with 5% CO2. Nuclei from approximately 10 million formaldehyde crosslinked (1%; 10min at room temperature) cells were isolated and chromatin was fragmented using sonicator (bioruptor). Lysates were cleared and protein-DNA complexes were isolated using target specific antibodies and protein-A/G magnetic beads. DNA fragments were purified and libraries were prepared accorcing to standard Illumina protocol. NextSeq 500 gds 304152134 GSM4152134 GEO Accession GSM4152134 SRX7107233 GSM4152135 SRP228821 SRS5618420 GSM4152135 ChIP-Seq GENOMIC ChIP VCaP cells were grown in DMEM medium supplemented with 10% feta bovine serum and 1% penicillin/streptomycin antibiotics at 37 degree C temperature incubator with 5% CO2. Nuclei from approximately 10 million formaldehyde crosslinked (1%; 10min at room temperature) cells were isolated and chromatin was fragmented using sonicator (bioruptor). Lysates were cleared and protein-DNA complexes were isolated using target specific antibodies and protein-A/G magnetic beads. DNA fragments were purified and libraries were prepared accorcing to standard Illumina protocol. NextSeq 500 gds 304152135 GSM4152135 GEO Accession GSM4152135 SRX7708034 GSM4306529 SRP228821 PRJNA588093 SRS6131726 GSM4306529 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306529 GSM4306529 GEO Accession GSM4306529 SRX7708035 GSM4306530 SRP228821 PRJNA588093 SRS6131727 GSM4306530 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306530 GSM4306530 GEO Accession GSM4306530 SRX7708036 GSM4306531 SRP228821 PRJNA588093 SRS6131728 GSM4306531 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306531 GSM4306531 GEO Accession GSM4306531 SRX7708037 GSM4306532 SRP228821 PRJNA588093 SRS6131729 GSM4306532 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306532 GSM4306532 GEO Accession GSM4306532 SRX7708038 GSM4306533 SRP228821 PRJNA588093 SRS6131730 GSM4306533 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306533 GSM4306533 GEO Accession GSM4306533 SRX7708039 GSM4306534 SRP228821 PRJNA588093 SRS6131731 GSM4306534 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306534 GSM4306534 GEO Accession GSM4306534 SRX7708046 GSM4306541 SRP228821 PRJNA588093 SRS6131738 GSM4306541 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306541 GSM4306541 GEO Accession GSM4306541 SRX7708047 GSM4306542 SRP228821 PRJNA588093 SRS6131739 GSM4306542 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306542 GSM4306542 GEO Accession GSM4306542 SRX7708048 GSM4306543 SRP228821 PRJNA588093 SRS6131740 GSM4306543 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306543 GSM4306543 GEO Accession GSM4306543 SRX7708049 GSM4306544 SRP228821 PRJNA588093 SRS6131741 GSM4306544 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306544 GSM4306544 GEO Accession GSM4306544 SRX7708050 GSM4306545 SRP228821 PRJNA588093 SRS6131742 GSM4306545 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306545 GSM4306545 GEO Accession GSM4306545 SRX7708051 GSM4306546 SRP228821 PRJNA588093 SRS6131743 GSM4306546 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). NextSeq 500 gds 304306546 GSM4306546 GEO Accession GSM4306546 SRX9270540 GSM4826444 SRP228821 PRJNA588093 SRS7499410 GSM4826444 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826444 GSM4826444 GEO Accession GSM4826444 SRX9270541 GSM4826445 SRP228821 PRJNA588093 SRS7499411 GSM4826445 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826445 GSM4826445 GEO Accession GSM4826445 SRX9270542 GSM4826446 SRP228821 PRJNA588093 SRS7499412 GSM4826446 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826446 GSM4826446 GEO Accession GSM4826446 SRX9270543 GSM4826447 SRP228821 PRJNA588093 SRS7499413 GSM4826447 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826447 GSM4826447 GEO Accession GSM4826447 SRX9270544 GSM4826448 SRP228821 PRJNA588093 SRS7499414 GSM4826448 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826448 GSM4826448 GEO Accession GSM4826448 SRX9270545 GSM4826449 SRP228821 PRJNA588093 SRS7499415 GSM4826449 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826449 GSM4826449 GEO Accession GSM4826449 SRX9270546 GSM4826450 SRP228821 PRJNA588093 SRS7499416 GSM4826450 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826450 GSM4826450 GEO Accession GSM4826450 SRX9270547 GSM4826451 SRP228821 PRJNA588093 SRS7499417 GSM4826451 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826451 GSM4826451 GEO Accession GSM4826451 SRX9270548 GSM4826452 SRP228821 PRJNA588093 SRS7499418 GSM4826452 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826452 GSM4826452 GEO Accession GSM4826452 SRX9270549 GSM4826453 SRP228821 PRJNA588093 SRS7499419 GSM4826453 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826453 GSM4826453 GEO Accession GSM4826453 SRX9270550 GSM4826454 SRP228821 PRJNA588093 SRS7499420 GSM4826454 OTHER TRANSCRIPTOMIC other RNA was extracted using Trizol per manufactures protocol, with addition of DTT, and protection from light during the procedure to prevent S-S cross-binding. 5 ug of RNA was used for SLAMseq modifications, as described in Herzog et. al. 2017. Briefly, Iodoacetamide (Sigma I1149) was conjugated to 4SU in a 50mM pH 8.0 phosphate buffer in DMSO/Water (1:1), the reaction was quenched with DTT and RNA was reprecipitated using Ethanol and NaOAc. Libraries were prepared using Quantseq 3' mRNA-Seq Library Prep Kit (Lexogen). Illumina NovaSeq 6000 gds 304826454 GSM4826454 GEO Accession GSM4826454