ID: 132090047 | Neanderthal introgressed variant-containing enhancer experimental_25764 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130191000..130191169) | | |
ID: 132090046 | Neanderthal introgressed variant-containing enhancer experimental_25722 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130145973..130146142) | | |
ID: 132090045 | Neanderthal introgressed variant-containing enhancer experimental_25704 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130138128..130138297) | | |
ID: 132090044 | Neanderthal introgressed variant-containing enhancer experimental_25699 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130137174..130137343) | | |
ID: 127825696 | H3K4me1 hESC enhancer GRCh37_chr12:130682728-130683228 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130198183..130198683) | | |
ID: 127825695 | H3K4me1 hESC enhancer GRCh37_chr12:130677479-130677979 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130192934..130193434) | | |
ID: 127825694 | H3K4me1 hESC enhancer GRCh37_chr12:130667832-130668510 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130183287..130183965) | | |
ID: 127825693 | NANOG hESC enhancer GRCh37_chr12:130649290-130649835 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130164745..130165290) | | |
ID: 127825692 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:130648209-130649204 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130163664..130164659) | | |
ID: 127825691 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:130646056-130646622 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130161511..130162077) | | |
ID: 127825690 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:130645489-130646055 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130160944..130161510) | | |
ID: 127825689 | H3K4me1 hESC enhancer GRCh37_chr12:130616321-130616838 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130131776..130132293) | | |
ID: 127825688 | H3K4me1 hESC enhancer GRCh37_chr12:130615804-130616320 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130131259..130131775) | | |
ID: 127825687 | H3K4me1 hESC enhancer GRCh37_chr12:130615286-130615803 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130130741..130131258) | | |
ID: 127825686 | H3K4me1 hESC enhancer GRCh37_chr12:130597592-130598092 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130113047..130113547) | | |
ID: 127825685 | H3K4me1 hESC enhancer GRCh37_chr12:130572501-130573018 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130087956..130088473) | | |
ID: 127825684 | H3K4me1 hESC enhancer GRCh37_chr12:130571983-130572500 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130087438..130087955) | | |
ID: 127825683 | NANOG hESC enhancer GRCh37_chr12:130560143-130560670 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130075598..130076125) | | |
ID: 124903088 | uncharacterized LOC124903088 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130133382..130140832) | | |
ID: 124849283 | Sharpr-MPRA regulatory region 11699 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (130195964..130196258) | | |