ID: 132090209 | Neanderthal introgressed variant-containing enhancer experimental_33604 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100889485..100889654) | | |
ID: 132090208 | Neanderthal introgressed variant-containing enhancer experimental_33596 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100888656..100888825) | | |
ID: 132090207 | Neanderthal introgressed variant-containing enhancer experimental_33586 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100873672..100873841) | | |
ID: 132090206 | Neanderthal introgressed variant-containing enhancer experimental_33583 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100867539..100867708) | | |
ID: 129663501 | ReSE screen-validated silencer GRCh37_chr14:101343532-101343742 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100877195..100877405) | | |
ID: 127828643 | H3K4me1 hESC enhancer GRCh37_chr14:101357417-101357918 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100891080..100891581) | | |
ID: 127828642 | H3K4me1 hESC enhancer GRCh37_chr14:101321295-101321796 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100854958..100855459) | | |
ID: 127828641 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:101306417-101307176 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100840080..100840839) | | |
ID: 127828640 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:101305655-101306416 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100839318..100840079) | | |
ID: 127828639 | NANOG hESC enhancer GRCh37_chr14:101296990-101297491 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100830653..100831154) | | |
ID: 127828638 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:101290055-101290755 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100823718..100824418) | | |
ID: 127828637 | H3K27ac hESC enhancer GRCh37_chr14:101281498-101281998 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100815161..100815661) | | |
ID: 127828636 | H3K27ac hESC enhancer GRCh37_chr14:101275541-101276109 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100809204..100809772) | | |
ID: 127828635 | H3K4me1 hESC enhancer GRCh37_chr14:101272538-101273453 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100806201..100807116) | | |
ID: 127828634 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:101251634-101252164 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100785297..100785827) | | |
ID: 125078039 | Sharpr-MPRA regulatory region 13483 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100885692..100885986) | | |
ID: 112163682 | Sharpr-MPRA regulatory region 10698 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100771192..100771486) | | |
ID: 100616495 | microRNA 2392 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100814491..100814574) | | |
ID: 100126315 | microRNA 665 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100875033..100875104) | MIRN665, hsa-mir-665, mir-665 | |
ID: 768222 | microRNA 770 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100852390..100852487) | MIRN770, hsa-mir-770 | |