| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:68433809-68434107 | Common:2; Rare:38 | ||||
| chrX:68498958-68499056 | Rare:23 | ||||
| chrX:68828837-68829030 | Rare:38 | ||||
| chrX:71118427-71118748 | Common:1; Rare:62; Clinvar (benign):2 | ||||
| chrX:71254103-71254339 | Common:1; Rare:41 | ||||
| chrX:71254681-71254797 | Common:1; Rare:12 | ||||
| chrX:71365896-71366252 | Common:4; Rare:65 | ||||
| chrX:72181302-72181341 | Common:1; Rare:8 | ||||
| chrX:72714061-72714406 | Common:2; Rare:67; Clinvar (benign):1 | ||||
| chrX:73563044-73563303 | Common:1; Rare:38 | ||||
| chrX:74614483-74614833 | Common:1; Rare:79 | ||||
| chrX:75156262-75156369 | Common:2; Rare:29 | ||||
| chrX:75273991-75274223 | Rare:32 | ||||
| chrX:75523009-75523225 | Common:1; Rare:46 | ||||
| chrX:75523244-75523443 | Common:1; Rare:29 |