ID: 132090082 | Neanderthal introgressed variant-containing enhancer experimental_26902 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26250596..26250765) | | |
ID: 132090081 | Neanderthal introgressed variant-containing enhancer experimental_26866 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26214993..26215162) | | |
ID: 132090080 | Neanderthal introgressed variant-containing enhancer experimental_26717 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25899195..25899364) | | |
ID: 130007570 | ATAC-STARR-seq lymphoblastoid active region 6118 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26245267..26245446) | | |
ID: 130007569 | ATAC-STARR-seq lymphoblastoid silent region 4301 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26126449..26126618) | | |
ID: 130007568 | ATAC-STARR-seq lymphoblastoid silent region 4300 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26114160..26114509) | | |
ID: 130007567 | ATAC-STARR-seq lymphoblastoid silent region 4299 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26097126..26097195) | | |
ID: 130007566 | ATAC-STARR-seq lymphoblastoid silent region 4298 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25959244..25959293) | | |
ID: 130007565 | ATAC-STARR-seq lymphoblastoid silent region 4297 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25959054..25959103) | | |
ID: 130007564 | ATAC-STARR-seq lymphoblastoid silent region 4296 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25958884..25958983) | | |
ID: 130007563 | ATAC-STARR-seq lymphoblastoid silent region 4295 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25958294..25958783) | | |
ID: 127823837 | H3K4me1 hESC enhancer GRCh37_chr12:26379181-26379816 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26226248..26226883) | | |
ID: 127823836 | OCT4-NANOG hESC enhancer GRCh37_chr12:26200376-26200975 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26047443..26048042) | | |
ID: 127823835 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:26151265-26152021 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25998332..25999088) | | |
ID: 127823834 | OCT4-NANOG hESC enhancer GRCh37_chr12:26040173-26040831 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25887240..25887898) | | |
ID: 127823833 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:26038654-26039197 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25885721..25886264) | | |
ID: 126861482 | MED14-independent group 3 enhancer GRCh37_chr12:26398995-26400194 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26246062..26247261) | | |
ID: 124902901 | uncharacterized LOC124902901 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26009948..26011388, complement) | | |
ID: 124629335 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:26150508-26151264 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25997575..25998331) | | |
ID: 107984501 | uncharacterized LOC107984501 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26004722..26005948, complement) | | |