| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:56232286-56232443 | Rare:23 | ||||
| chrX:56563458-56563674 | Rare:49; Clinvar:1 | ||||
| chrX:57121422-57121599 | Common:1; Rare:41 | ||||
| chrX:64205690-64205977 | Common:1; Rare:51 | ||||
| chrX:65034708-65034863 | Common:1; Rare:33 | ||||
| chrX:68433435-68433771 | Rare:63 | ||||
| chrX:68498968-68499059 | Rare:22 | ||||
| chrX:68693501-68693698 | Rare:48 | ||||
| chrX:70289863-70289972 | Rare:25 | ||||
| chrX:71111558-71111685 | Rare:14; Clinvar:2 | ||||
| chrX:71118641-71118741 | Rare:27; Clinvar (benign):2 | ||||
| chrX:71296827-71297182 | Common:1; Rare:50 | ||||
| chrX:74614433-74614816 | Common:1; Rare:85 | ||||
| chrX:75156251-75156315 | Common:1; Rare:21 | ||||
| chrX:75523009-75523159 | Rare:34 |