| ID: 129665012 | ReSE screen-validated silencer GRCh37_chrX:138226529-138226732 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (139144367..139144570) | | |
| ID: 127898408 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:138424361-138425018 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (139342202..139342859) | | |
| ID: 127898407 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:138423703-138424360 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (139341544..139342201) | | |
| ID: 127898406 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:138307248-138307856 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (139225086..139225694) | | |
| ID: 127898405 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:138306638-138307247 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (139224476..139225085) | | |
| ID: 127898404 | NANOG hESC enhancer GRCh37_chrX:137842490-137843019 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (138760328..138760857) | | |
| ID: 126863331 | MED14-independent group 3 enhancer GRCh37_chrX:137859976-137861175 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (138777814..138779013) | | |
| ID: 124905222 | uncharacterized LOC124905222 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (139176387..139195860) | | |
| ID: 115482715 | H2A.Q variant histone 1, pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (138558996..138559298) | | |
| ID: 111429618 | NFE2L2 motif-containing MPRA enhancer 215 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (138925514..138925658) | | |
| ID: 100130620 | tropomyosin 2 pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (138806374..138807130) | | |
| ID: 100129662 | FGF13 antisense RNA 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (138712107..138716605) | | 301087 |
| ID: 727686 | SNRPN upstream open reading frame like (pseudogene) [Homo sapiens (human)] | Chromosome X, NC_000023.11 (139361940..139362482) | CXorf19 | |
| ID: 574507 | microRNA 504 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (138667711..138667793, complement) | MIRN504, hsa-mir-504, mir-504 | |
| ID: 2258 | fibroblast growth factor 13 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (138614727..139205023, complement) | DEE90, FGF-13, FGF2, FHF-2, FHF2, LINC00889, XLID110 | 300070 |