Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:48597372-48597543 | Rare:27 | ||||
chrX:49079842-49079983 | Rare:24 | ||||
chrX:53422639-53422833 | Common:1; Rare:48 | ||||
chrX:54440240-54440423 | Rare:27 | ||||
chrX:54809503-54809784 | Common:1; Rare:43 | ||||
chrX:55161097-55161307 | Rare:63 | ||||
chrX:57121495-57121610 | Common:1; Rare:25 | ||||
chrX:68498965-68499049 | Rare:20 | ||||
chrX:70289879-70290130 | Rare:47 | ||||
chrX:71068316-71068668 | Common:2; Rare:79 | ||||
chrX:74614483-74614886 | Common:1; Rare:91 | ||||
chrX:75156269-75156315 | Common:1; Rare:11 | ||||
chrX:76172943-76173134 | Rare:43 | ||||
chrX:77895412-77895750 | Rare:93; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chrX:81201889-81202203 | Rare:53 |