ID: 132090568 | Neanderthal introgressed variant-containing enhancer experimental_59894 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16581376..16581545) | | |
ID: 132090567 | Neanderthal introgressed variant-containing enhancer experimental_59877 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16547807..16547976) | | |
ID: 130065445 | ATAC-STARR-seq lymphoblastoid silent region 12682 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16392648..16392707) | | |
ID: 130065444 | ATAC-STARR-seq lymphoblastoid active region 17561 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16317671..16318190) | | |
ID: 130065443 | ATAC-STARR-seq lymphoblastoid active region 17560 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (15986226..15986275) | | |
ID: 130065442 | ATAC-STARR-seq lymphoblastoid active region 17559 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (15985986..15986165) | | |
ID: 130065441 | ATAC-STARR-seq lymphoblastoid active region 17558 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (15980183..15980352) | | |
ID: 130065440 | ATAC-STARR-seq lymphoblastoid active region 17557 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (15923260..15923419) | | |
ID: 129664568 | ReSE screen-validated silencer GRCh37_chr20:16456599-16456834 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16475954..16476189) | | |
ID: 127892635 | H3K27ac hESC enhancer GRCh37_chr20:16553850-16554371 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16573205..16573726) | | |
ID: 127892634 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:16240179-16240692 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16259534..16260047) | | |
ID: 127892633 | H3K27ac hESC enhancer GRCh37_chr20:16208020-16208897 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16227375..16228252) | | |
ID: 127892632 | H3K27ac hESC enhancer GRCh37_chr20:16187781-16188280 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16207136..16207635) | | |
ID: 127892631 | H3K27ac hESC enhancer GRCh37_chr20:16187279-16187780 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16206634..16207135) | | |
ID: 126862980 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr20:16417298-16418497 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16436653..16437852) | | |
ID: 125384588 | Sharpr-MPRA regulatory region 3089 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16479724..16480018) | | |
ID: 125384587 | Sharpr-MPRA regulatory region 7814 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16322564..16322858) | | |
ID: 124904875 | uncharacterized LOC124904875 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16575303..16579359) | | |
ID: 124904874 | uncharacterized LOC124904874 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16177914..16222533, complement) | | |
ID: 121627894 | Sharpr-MPRA regulatory region 11342 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16241924..16242218) | | |