ERX8503474 E-MTAB-11478:Diploid rep1_1_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777077 SAMEA13173519 Diploid rep1_1_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 2n ERX8503475 E-MTAB-11478:Diploid rep1_2_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777078 SAMEA13173520 Diploid rep1_2_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 2n ERX8503476 E-MTAB-11478:Diploid rep2_1_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777079 SAMEA13173521 Diploid rep2_1_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 2n ERX8503477 E-MTAB-11478:Diploid rep2_2_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777080 SAMEA13173522 Diploid rep2_2_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 2n ERX8503478 E-MTAB-11478:Diploid Xi_1_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777081 SAMEA13173523 Diploid Xi_1_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 2n ERX8503479 E-MTAB-11478:Diploid Xi_2_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777082 SAMEA13173524 Diploid Xi_2_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 2n ERX8503480 E-MTAB-11478:Haploid rep1_1_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777083 SAMEA13173525 Haploid rep1_1_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 1n ERX8503481 E-MTAB-11478:Haploid rep1_2_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777084 SAMEA13173526 Haploid rep1_2_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 1n ERX8503482 E-MTAB-11478:Haploid rep2_1_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777085 SAMEA13173527 Haploid rep2_1_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 1n ERX8503483 E-MTAB-11478:Haploid rep2_2_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777086 SAMEA13173528 Haploid rep2_2_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 1n ERX8503484 E-MTAB-11478:Triploid clone H_1_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777087 SAMEA13173529 Triploid clone H_1_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 3n ERX8503485 E-MTAB-11478:Triploid clone H_2_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777088 SAMEA13173530 Triploid clone H_2_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 3n ERX8503486 E-MTAB-11478:Triploid clone K_1_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777089 SAMEA13173531 Triploid clone K_1_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 3n ERX8503487 E-MTAB-11478:Triploid clone K_2_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777090 SAMEA13173532 Triploid clone K_2_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 3n ERX8503488 E-MTAB-11478:Triploid clone L_1_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777091 SAMEA13173533 Triploid clone L_1_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 3n ERX8503489 E-MTAB-11478:Triploid clone L_2_s ERP135774 PRJEB51174 Reduced representation bisulfite sequencing (RRBS) of haploid, diploid and triploid hESCs ERS10777092 SAMEA13173534 Triploid clone L_2_s Bisulfite-Seq GENOMIC Reduced Representation Cells were washed with PBS and trypsinized gSYNC DNA extraction kit (Geneaid) The DNA was digested with MspI (NEB), Subsequently, bisulfite treatment was conducted using the ZYMO EZ DNA Methylation-Gold Kit. The converted DNAs are then amplified by twelve cycles of PCR, using 25 μl KAPA HiFi HotStart Uracil+ ReadyMix HiSeq X Ten Experimental Factor: ploidy 3n