| ID: 127460545 | H3K4me1 hESC enhancer GRCh37_chr8:142218923-142219430 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141208824..141209331) | | |
| ID: 127460544 | H3K4me1 hESC enhancer GRCh37_chr8:142218415-142218922 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141208316..141208823) | | |
| ID: 127460543 | H3K4me1 hESC enhancer GRCh37_chr8:142202725-142203225 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141192626..141193126) | | |
| ID: 127460542 | H3K4me1 hESC enhancer GRCh37_chr8:142202224-142202724 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141192125..141192625) | | |
| ID: 127460541 | H3K4me1 hESC enhancer GRCh37_chr8:142194501-142195455 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141184402..141185356) | | |
| ID: 127460540 | H3K4me1 hESC enhancer GRCh37_chr8:142191187-142191687 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141181088..141181588) | | |
| ID: 127460539 | H3K4me1 hESC enhancer GRCh37_chr8:142183517-142184016 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141173418..141173917) | | |
| ID: 127460538 | H3K4me1 hESC enhancer GRCh37_chr8:142183015-142183516 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141172916..141173417) | | |
| ID: 127460537 | H3K4me1 hESC enhancer GRCh37_chr8:142167099-142167874 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141157000..141157775) | | |
| ID: 127460536 | H3K4me1 hESC enhancer GRCh37_chr8:142163840-142164798 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141153741..141154699) | | |
| ID: 127460535 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:142144757-142145375 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141134658..141135276) | | |
| ID: 127460534 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:142138949-142139779 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141128135..141129680) | | |
| ID: 127460533 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:142137284-142138115 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141127185..141128016) | | |
| ID: 127460532 | H3K4me1 hESC enhancer GRCh37_chr8:142128597-142129165 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141118498..141119066) | | |
| ID: 124188242 | Sharpr-MPRA regulatory region 5779 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141164650..141164944) | | |
| ID: 105375785 | uncharacterized LOC105375785 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141197989..141203359, complement) | | |
| ID: 101927963 | DENND3 antisense RNA 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141124678..141130141, complement) | | |
| ID: 57210 | solute carrier family 45 member 4 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141207174..141308288, complement) | | 619581 |
| ID: 22898 | DENN domain containing 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (141128589..141195804) | | 617503 |