ID: 132089347 | Neanderthal introgressed variant-containing enhancer experimental_90037 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133983465..133983634) | | |
ID: 132089346 | Neanderthal introgressed variant-containing enhancer experimental_90028 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133964673..133964842) | | |
ID: 132089345 | Neanderthal introgressed variant-containing enhancer experimental_90026 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133962885..133963054) | | |
ID: 129997188 | ATAC-STARR-seq lymphoblastoid silent region 17556 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (134093382..134093451) | | |
ID: 129997187 | ATAC-STARR-seq lymphoblastoid active region 25081 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133967026..133967075) | | |
ID: 129997186 | ATAC-STARR-seq lymphoblastoid silent region 17555 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133952222..133952331) | | |
ID: 129997185 | ATAC-STARR-seq lymphoblastoid silent region 17554 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133837965..133838014) | | |
ID: 128092253 | umcharacterized LOC128092253 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133953304..133980088) | | |
ID: 127407279 | H3K27ac hESC enhancer GRCh37_chr6:134382163-134382827 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (134061025..134061689) | | |
ID: 127407278 | NANOG-H3K27ac hESC enhancer GRCh37_chr6:134381498-134382162 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (134060360..134061024) | | |
ID: 127407277 | H3K4me1 hESC enhancer GRCh37_chr6:134213614-134214222 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133892476..133893084) | | |
ID: 127407276 | H3K4me1 hESC enhancer GRCh37_chr6:134211964-134212728 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133890826..133891590) | | |
ID: 127407275 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr6:134209799-134210712 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133888661..133889574) | | |
ID: 127407274 | NANOG-H3K4me1 hESC enhancer GRCh37_chr6:134175312-134176050 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133854174..133854912) | | |
ID: 124901404 | uncharacterized LOC124901404 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (134082047..134121433) | | |
ID: 100507308 | TCF21 antisense RNA inducing promoter demethylation [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133502252..133889006, complement) | EYA4-AS1 | 616058 |
ID: 100421250 | epithelial splicing regulatory protein 1 pseudogene [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (134009008..134009547) | | |
ID: 387065 | high mobility group AT-hook 1 pseudogene 7 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (134113962..134117680, complement) | HMGA1L7 | |
ID: 154091 | solute carrier family 2 member 12 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133987581..134052624, complement) | GLUT12, GLUT8 | 610372 |
ID: 154089 | long intergenic non-protein coding RNA 1312 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133821147..133853992) | | |