ID: 132090070 | Neanderthal introgressed variant-containing enhancer experimental_26510 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21969188..21969357) | | |
ID: 130007534 | ATAC-STARR-seq lymphoblastoid active region 6096 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21795417..21795466) | | |
ID: 130007533 | ATAC-STARR-seq lymphoblastoid active region 6094 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21657514..21657763) | | |
ID: 130007532 | ATAC-STARR-seq lymphoblastoid active region 6093 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21657394..21657483) | | |
ID: 127823807 | OCT4-NANOG hESC enhancer GRCh37_chr12:22201245-22201850 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22048311..22048916) | | |
ID: 127823806 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:22199579-22200284 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22046645..22047350) | | |
ID: 127823805 | H3K4me1 hESC enhancer GRCh37_chr12:22093793-22094770 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21940859..21941836) | | |
ID: 127823804 | H3K4me1 hESC enhancer GRCh37_chr12:22052631-22053131 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21899697..21900197) | | |
ID: 127823803 | H3K4me1 hESC enhancer GRCh37_chr12:22052130-22052630 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21899196..21899696) | | |
ID: 127823802 | H3K4me1 hESC enhancer GRCh37_chr12:21926997-21927994 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21774063..21775120) | | |
ID: 127823801 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:21810675-21811203 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21657741..21658323) | | |
ID: 127823800 | OCT4-NANOG hESC enhancer GRCh37_chr12:21748286-21748889 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21595352..21595955) | | |
ID: 126861480 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:21710858-21712057 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21557924..21559123) | | |
ID: 124902896 | uncharacterized LOC124902896 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21534594..21537333) | | |
ID: 124629328 | H3K4me1 hESC enhancer GRCh37_chr12:21925998-21926996 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21773064..21774062) | | |
ID: 112163548 | Sharpr-MPRA regulatory region 13841 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22046035..22046471) | | |
ID: 110121489 | VISTA enhancer hs2151 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21891137..21892666) | | |
ID: 105369690 | uncharacterized LOC105369690 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22063773..22082527, complement) | | |
ID: 105369689 | uncharacterized LOC105369689 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21662313..21829261) | | |
ID: 102724261 | uncharacterized LOC102724261 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21725611..21757870, complement) | | |