ID: 132090868 | Neanderthal introgressed variant-containing enhancer experimental_34259 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56515280..56515449) | | |
ID: 132090221 | Neanderthal introgressed variant-containing enhancer experimental_34331 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56675125..56675294) | | |
ID: 132090220 | Neanderthal introgressed variant-containing enhancer experimental_34318 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56554768..56554937) | | |
ID: 132090219 | Neanderthal introgressed variant-containing enhancer experimental_34296 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56534428..56534597) | | |
ID: 132090218 | Neanderthal introgressed variant-containing enhancer experimental_34274 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56522307..56522476) | | |
ID: 132090217 | Neanderthal introgressed variant-containing enhancer experimental_34268 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56517936..56518105) | | |
ID: 130055718 | ATAC-STARR-seq lymphoblastoid silent region 5790 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56579866..56580085) | | |
ID: 130055717 | ATAC-STARR-seq lymphoblastoid active region 8437 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56199192..56199381) | | |
ID: 130055716 | ATAC-STARR-seq lymphoblastoid silent region 5789 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56118819..56118888) | | |
ID: 130055715 | ATAC-STARR-seq lymphoblastoid silent region 5788 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56118269..56118528) | | |
ID: 129663435 | ReSE screen-validated silencer GRCh37_chr14:57028256-57028447 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56561538..56561729) | | |
ID: 127827632 | NANOG hESC enhancer GRCh37_chr14:57115102-57115779 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56648384..56649061) | | |
ID: 127827631 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr14:56991474-56992081 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56524756..56525363) | | |
ID: 127827630 | H3K4me1 hESC enhancer GRCh37_chr14:56919899-56920398 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56453181..56453680) | | |
ID: 127827629 | H3K4me1 hESC enhancer GRCh37_chr14:56919397-56919898 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56452679..56453180) | | |
ID: 127827628 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:56914291-56914896 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56447573..56448178) | | |
ID: 127827627 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:56913685-56914290 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56446967..56447572) | | |
ID: 127827626 | H3K4me1 hESC enhancer GRCh37_chr14:56763567-56764066 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56296849..56297348) | | |
ID: 127827625 | H3K4me1 hESC enhancer GRCh37_chr14:56717288-56717788 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56250570..56251070) | | |
ID: 126861954 | MED14-independent group 3 enhancer GRCh37_chr14:57132632-57133831 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56665914..56667113) | | |