ID: 129664979 | ReSE screen-validated silencer GRCh37_chrX:88660958-88661203 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89405959..89406204) | | |
ID: 127897878 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:88962129-88962877 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89707130..89707878) | | |
ID: 127897877 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:88961378-88962128 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89706379..89707129) | | |
ID: 127897876 | OCT4-NANOG hESC enhancer GRCh37_chrX:88687522-88688285 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89432523..89433286) | | |
ID: 102724150 | uncharacterized LOC102724150 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89403129..89455254) | | |
ID: 100499485 | sorcin pseudogene 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89367436..89367697, complement) | | |
ID: 100130134 | STAU2 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (90037863..90040928, complement) | | |
ID: 254700 | USP12 pseudogene X-linked [Homo sapiens (human)] | Chromosome X, NC_000023.11 (90112475..90115029) | USP12P2 | |
ID: 90316 | TGFB induced factor homeobox 2 like X-linked [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89921908..89922883) | TGIFLX | 300411 |