ID: 129664978 | ReSE screen-validated silencer GRCh37_chrX:88193497-88193682 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88938496..88938681) | | |
ID: 127897875 | H3K4me1 hESC enhancer GRCh37_chrX:88547967-88548466 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89292968..89293467) | | |
ID: 127897874 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:88419006-88419572 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89164006..89164572) | | |
ID: 127897873 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:88418438-88419005 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89163438..89164005) | | |
ID: 127897872 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:88238077-88238665 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88983076..88983664) | | |
ID: 127897871 | NANOG hESC enhancer GRCh37_chrX:88083247-88083748 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88828246..88828747) | | |
ID: 127897870 | H3K27ac hESC enhancer GRCh37_chrX:87994167-87994667 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88739166..88739666) | | |
ID: 127897869 | OCT4-NANOG hESC enhancer GRCh37_chrX:87498837-87499672 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88243836..88244671) | | |
ID: 126863288 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:87990232-87991431 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88735231..88736430) | | |
ID: 124900505 | small nucleolar RNA ACA64 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88148792..88148918) | | |
ID: 121853061 | Sharpr-MPRA regulatory region 3371 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88887008..88887302) | | |
ID: 107985713 | uncharacterized LOC107985713 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88494130..88613490, complement) | | |
ID: 107985653 | uncharacterized LOC107985653 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88984714..88989974) | | |
ID: 100499485 | sorcin pseudogene 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (89367436..89367697, complement) | | |
ID: 53336 | CPX chromosome region candidate 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (88747225..88754781) | CT77 | 301055 |