ID: 132090606 | Neanderthal introgressed variant-containing enhancer experimental_61302 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63881641..63881810) | | |
ID: 132090605 | Neanderthal introgressed variant-containing enhancer experimental_61295 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63880930..63881099) | | |
ID: 132090604 | Neanderthal introgressed variant-containing enhancer experimental_61287 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63878169..63878338) | | |
ID: 130066404 | ATAC-STARR-seq lymphoblastoid active region 18254 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63863998..63864227) | | |
ID: 130066403 | ATAC-STARR-seq lymphoblastoid silent region 13189 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63858546..63858705) | | |
ID: 130066402 | ATAC-STARR-seq lymphoblastoid silent region 13188 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63854597..63854646) | | |
ID: 130066401 | ATAC-STARR-seq lymphoblastoid active region 18253 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63851226..63851325) | | |
ID: 130066400 | ATAC-STARR-seq lymphoblastoid active region 18252 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63850986..63851145) | | |
ID: 130066399 | ATAC-STARR-seq lymphoblastoid silent region 13187 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63831282..63831421) | | |
ID: 130066398 | ATAC-STARR-seq lymphoblastoid active region 18251 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63782340..63782399) | | |
ID: 129664683 | ReSE screen-validated silencer GRCh37_chr20:62517585-62517755 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63886232..63886402) | | |
ID: 129664682 | ReSE screen-validated silencer GRCh37_chr20:62477766-62477915 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63846413..63846562) | | |
ID: 129664681 | ReSE screen-validated silencer GRCh37_chr20:62401989-62402163 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63770636..63770810) | | |
ID: 127894291 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62497355-62498074 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63866002..63866721) | | |
ID: 127894290 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62484853-62485706 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63853500..63854353) | | |
ID: 127894289 | H3K4me1 hESC enhancer GRCh37_chr20:62475261-62475938 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63843908..63844585) | | |
ID: 127894288 | H3K4me1 hESC enhancer GRCh37_chr20:62460361-62461052 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63829008..63829699) | | |
ID: 127894287 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62447119-62447869 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63815766..63816516) | | |
ID: 127894286 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62446368-62447118 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63815015..63815765) | | |
ID: 127894285 | H3K4me1 hESC enhancer GRCh37_chr20:62433537-62434038 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63802184..63802685) | | |