ID: 127268828 | H3K27ac hESC enhancer GRCh37_chr1:39811169-39811670 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39345497..39345998) | | |
ID: 127268827 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:39698122-39698932 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39232450..39233260) | | |
ID: 127268826 | OCT4-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:39679473-39680191 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39213801..39214519) | | |
ID: 127268825 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:39657180-39657722 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39191508..39192050) | | |
ID: 127268824 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:39637465-39637991 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39171793..39172319) | | |
ID: 127268823 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:39607555-39608294 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39141883..39142622) | | |
ID: 127268822 | H3K27ac hESC enhancer GRCh37_chr1:39606647-39607470 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39140975..39141798) | | |
ID: 127268821 | H3K27ac hESC enhancer GRCh37_chr1:39605822-39606646 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39140150..39140974) | | |
ID: 127268820 | H3K4me1 hESC enhancer GRCh37_chr1:39599569-39600336 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39133897..39134664) | | |
ID: 127268819 | NANOG-H3K27ac hESC enhancer GRCh37_chr1:39568667-39569222 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39102995..39103550) | | |
ID: 127268818 | NANOG hESC enhancer GRCh37_chr1:39517634-39518135 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39051962..39052463) | | |
ID: 127268817 | H3K27ac hESC enhancer GRCh37_chr1:39492550-39493135 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39026878..39027463) | | |
ID: 127268816 | H3K27ac hESC enhancer GRCh37_chr1:39491963-39492549 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39026182..39026877) | | |
ID: 126805711 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:39824023-39825222 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39358351..39359550) | | |
ID: 126805710 | MED14-independent group 3 enhancer GRCh37_chr1:39812278-39813477 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39346606..39347805) | | |
ID: 126805709 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:39648813-39650012 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39183141..39184609) | | |
ID: 124904101 | uncharacterized LOC124904101 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39486956..39491548, complement) | | |
ID: 124904088 | uncharacterized LOC124904088 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39038017..39061873) | | |
ID: 122056843 | Sharpr-MPRA regulatory region 6545 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39196877..39197171) | | |
ID: 120893132 | Sharpr-MPRA regulatory region 301 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39133117..39133411) | | |