ID: 132090201 | Neanderthal introgressed variant-containing enhancer experimental_33303 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73960816..73960985) | | |
ID: 132090200 | Neanderthal introgressed variant-containing enhancer experimental_33301 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73956068..73956237) | | |
ID: 132090199 | Neanderthal introgressed variant-containing enhancer experimental_33300 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73955851..73956020) | | |
ID: 132090198 | Neanderthal introgressed variant-containing enhancer experimental_33299 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73954112..73954281) | | |
ID: 130009885 | ATAC-STARR-seq lymphoblastoid active region 7820 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74158047..74158156) | | |
ID: 130009884 | ATAC-STARR-seq lymphoblastoid silent region 5399 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74134151..74135900) | | |
ID: 130009883 | ATAC-STARR-seq lymphoblastoid active region 7819 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74133092..74133141) | | |
ID: 130009882 | ATAC-STARR-seq lymphoblastoid active region 7818 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74132882..74133061) | | |
ID: 130009881 | ATAC-STARR-seq lymphoblastoid active region 7817 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74026803..74026882) | | |
ID: 128966561 | uncharacterized LOC128966561 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73578306..73595519, complement) | | |
ID: 127826517 | NANOG hESC enhancer GRCh37_chr13:74875892-74876393 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74301755..74302256) | | |
ID: 127826516 | H3K4me1 hESC enhancer GRCh37_chr13:74861026-74861526 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74286889..74287389) | | |
ID: 127826515 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:74815323-74815876 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74241186..74241739) | | |
ID: 127826514 | NANOG hESC enhancer GRCh37_chr13:74749652-74750153 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74175515..74176016) | | |
ID: 127826513 | NANOG-H3K27ac hESC enhancer GRCh37_chr13:74610780-74611709 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74036643..74037572) | | |
ID: 127826512 | NANOG-H3K27ac hESC enhancer GRCh37_chr13:74609849-74610779 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (74035712..74036642) | | |
ID: 127826511 | OCT4-NANOG hESC enhancer GRCh37_chr13:74341622-74342257 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73767485..73768120) | | |
ID: 127826510 | NANOG-H3K27ac hESC enhancer GRCh37_chr13:74340128-74340628 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73765991..73766491) | | |
ID: 127826509 | OCT4-NANOG hESC enhancer GRCh37_chr13:74305638-74306208 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73731501..73732071) | | |
ID: 127826508 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:74214909-74215550 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (73640772..73641413) | | |