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: 132089923 | Neanderthal introgressed variant-containing enhancer experimental_20787 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22260433..22260602) | | |
ID: 130005442 | ATAC-STARR-seq lymphoblastoid active region 4532 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22193713..22193902) | | |
ID: 130005441 | ATAC-STARR-seq lymphoblastoid active region 4531 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22193373..22193462) | | |
ID: 130005440 | ATAC-STARR-seq lymphoblastoid silent region 3205 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22192903..22192952) | | |
ID: 130005439 | ATAC-STARR-seq lymphoblastoid active region 4530 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22192653..22192722) | | |
ID: 130005438 | ATAC-STARR-seq lymphoblastoid active region 4529 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22192563..22192622) | | |
ID: 127820636 | OCT4-NANOG hESC enhancer GRCh37_chr11:22255998-22256992 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22234452..22235446) | | |
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: 203859 | anoctamin 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22192473..22283357) | GDD1, LGMD2L, LGMDR12, TMEM16E | 608662 |
ID: 57084 | solute carrier family 17 member 6 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22338381..22379503) | DNPI, VGLUT2 | 607563 |