Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:55000242-55000415 | Rare:46 | ||||
chrX:55161108-55161269 | Rare:45 | ||||
chrX:57121440-57121591 | Common:1; Rare:35 | ||||
chrX:64205690-64206001 | Common:1; Rare:56 | ||||
chrX:65034697-65034827 | Common:1; Rare:26 | ||||
chrX:67543895-67544057 | Rare:27 | ||||
chrX:68498965-68499056 | Rare:22 | ||||
chrX:68693400-68693654 | Rare:55 | ||||
chrX:68828788-68829034 | Rare:54 | ||||
chrX:71095852-71096180 | Rare:39 | ||||
chrX:71223088-71223307 | Rare:26; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chrX:71283475-71283721 | Rare:40 | ||||
chrX:74421375-74421493 | Rare:29; Clinvar (benign):1 | ||||
chrX:75156273-75156315 | Common:1; Rare:11 | ||||
chrX:75273781-75274223 | Rare:57 |