| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71111569-71111723 | Rare:15; Clinvar:2 | ||||
| chrX:71254058-71254256 | Common:2; Rare:32 | ||||
| chrX:71254677-71254841 | Common:1; Rare:14 | ||||
| chrX:71283437-71283720 | Rare:45 | ||||
| chrX:71365915-71366250 | Common:4; Rare:60 | ||||
| chrX:71532882-71533154 | Rare:52 | ||||
| chrX:72305896-72306054 | Rare:31 | ||||
| chrX:73562981-73563303 | Common:1; Rare:56 | ||||
| chrX:74614478-74614820 | Common:1; Rare:76 | ||||
| chrX:75156273-75156395 | Common:2; Rare:29 | ||||
| chrX:75274582-75274702 | Common:2; Rare:24 | ||||
| chrX:75523014-75523233 | Common:1; Rare:45 | ||||
| chrX:75523239-75523546 | Common:3; Rare:42 | ||||
| chrX:77895412-77895741 | Rare:92; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103876-78104326 | Common:4; Rare:163 |