| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:74421288-74421607 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
| chrX:74614411-74614847 | Common:1; Rare:94 | ||||
| chrX:75156273-75156382 | Common:2; Rare:28 | ||||
| chrX:75274645-75274695 | Common:1; Rare:10 | ||||
| chrX:75523009-75523225 | Common:1; Rare:46 | ||||
| chrX:75523231-75523369 | Common:1; Rare:23 | ||||
| chrX:75523421-75523590 | Common:2; Rare:18 | ||||
| chrX:75785211-75785297 | Rare:25 | ||||
| chrX:76427613-76427728 | Rare:18 | ||||
| chrX:77895417-77895736 | Rare:86; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:77910561-77910745 | Common:1; Rare:27 | ||||
| chrX:78103962-78104289 | Common:4; Rare:111 | ||||
| chrX:78139571-78139718 | Common:1; Rare:75 | ||||
| chrX:81201784-81201842 | Rare:8 | ||||
| chrX:81201845-81202266 | Rare:66 |