ID: 127887103 | H3K4me1 hESC enhancer GRCh37_chr17:43900915-43901416 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45823549..45824050) | | |
ID: 127887102 | H3K4me1 hESC enhancer GRCh37_chr17:43890849-43891705 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45813483..45814339) | | |
ID: 127887101 | H3K4me1 hESC enhancer GRCh37_chr17:43884241-43884740 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45806875..45807374) | | |
ID: 127887100 | H3K4me1 hESC enhancer GRCh37_chr17:43883739-43884240 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45806373..45806874) | | |
ID: 127887099 | H3K4me1 hESC enhancer GRCh37_chr17:43869433-43869933 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45792067..45792567) | | |
ID: 127887098 | H3K4me1 hESC enhancer GRCh37_chr17:43862413-43862913 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45785047..45785547) | | |
ID: 127887096 | H3K4me1 hESC enhancer GRCh37_chr17:43840160-43840660 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45762794..45763294) | | |
ID: 127887095 | H3K4me1 hESC enhancer GRCh37_chr17:43835142-43835642 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45757776..45758276) | | |
ID: 127887094 | H3K4me1 hESC enhancer GRCh37_chr17:43828999-43829910 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45751633..45752544) | | |
ID: 127887093 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr17:43823543-43824208 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45746177..45746842) | | |
ID: 127887092 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr17:43822876-43823542 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45745510..45746176) | | |
ID: 127887091 | H3K4me1 hESC enhancer GRCh37_chr17:43695849-43696828 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45618483..45619462) | | |
ID: 127887090 | H3K4me1 hESC enhancer GRCh37_chr17:43677957-43678654 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45600591..45601288) | | |
ID: 126862576 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr17:43782244-43783443 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45704878..45706077) | | |
ID: 121852934 | Sharpr-MPRA regulatory region 9533 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45719803..45720097) | | |
ID: 108489980 | ARF GTPase 2, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45632945..45639402) | | |
ID: 107985028 | uncharacterized LOC107985028 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45731656..45734679, complement) | | |
ID: 105371802 | uncharacterized LOC105371802 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45657677..45670915, complement) | | |
ID: 104909134 | LINC02210-CRHR1 readthrough [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45620346..45835828) | CRHR1-IT1-CRHR1, MGC57346-CRHR1 | |
ID: 644191 | ribosomal protein S26 pseudogene 8 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45608540..45608987) | RPS26_20_1551 | |