ID: 127460784 | H3K4me1 hESC enhancer GRCh37_chr8:145060401-145061304 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143986123..143987136) | | |
ID: 127460783 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:145046871-145047718 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143972703..143973743) | | |
ID: 127460782 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:145046021-145046870 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143971853..143972702) | | |
ID: 127460781 | H3K4me1 hESC enhancer GRCh37_chr8:145040519-145041295 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143966351..143967127) | | |
ID: 127460780 | H3K4me1 hESC enhancer GRCh37_chr8:145039741-145040518 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143965573..143966350) | | |
ID: 127460779 | H3K4me1 hESC enhancer GRCh37_chr8:145038963-145039740 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143964795..143965572) | | |
ID: 127460778 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:145031501-145032404 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143957333..143958236) | | |
ID: 127460777 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:145024027-145024814 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143949859..143950646) | | |
ID: 127460776 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:145021665-145022452 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143947497..143948284) | | |
ID: 127460775 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:145020877-145021664 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143946709..143947496) | | |
ID: 127460774 | H3K4me1 hESC enhancer GRCh37_chr8:145006382-145007317 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143932214..143933149) | | |
ID: 127460773 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:144999476-145000347 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143925308..143926179) | | |
ID: 127460772 | H3K4me1 hESC enhancer GRCh37_chr8:144977006-144977576 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143902838..143903408) | | |
ID: 124902040 | uncharacterized LOC124902040 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143943864..143947787) | | |
ID: 124188248 | Sharpr-MPRA regulatory region 3935 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143990778..143991255) | | |
ID: 124188247 | Sharpr-MPRA regulatory region 5026 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143902501..143902795) | | |
ID: 121331314 | Sharpr-MPRA regulatory region 8265 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143940221..143940515) | | |
ID: 724031 | microRNA 661 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143945191..143945279, complement) | MIRN661, hsa-mir-661 | 613716 |
ID: 84875 | poly(ADP-ribose) polymerase family member 10 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143977158..144012764, complement) | ARTD10 | 609564 |
ID: 5339 | plectin [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143915153..143976745, complement) | EBS1, EBS5A, EBS5B, EBS5C, EBS5D, EBSMD, EBSND, EBSO, EBSOG, EBSPA, HD1, LGMD2Q, LGMDR17, PCN1, PLEC1b, PLTN, PLEC | 601282 |