ID: 132089925 | Neanderthal introgressed variant-containing enhancer experimental_20847 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22403420..22403589) | | |
ID: 132089924 | Neanderthal introgressed variant-containing enhancer experimental_20815 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22390793..22390962) | | |
ID: 130005444 | ATAC-STARR-seq lymphoblastoid active region 4534 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22624883..22624932) | | |
ID: 130005443 | ATAC-STARR-seq lymphoblastoid active region 4533 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22624713..22624872) | | |
ID: 127820637 | NANOG-H3K27ac hESC enhancer GRCh37_chr11:22646933-22647832 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22625313..22626286) | | |
ID: 126861161 | MED14-independent group 3 enhancer GRCh37_chr11:22306158-22307357 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22284575..22285811) | | |
ID: 120883619 | SLC17A6 divergent transcript [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22283730..22338222, complement) | | |
ID: 105376588 | uncharacterized LOC105376588 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22492087..22510400) | | |
ID: 102723378 | long intergenic non-protein coding RNA 1495 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22445672..22492019, complement) | | |
ID: 57084 | solute carrier family 17 member 6 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22338381..22379503) | DNPI, VGLUT2 | 607563 |
ID: 2188 | FA complementation group F [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22622533..22625823, complement) | FAF | 613897 |