| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154428457-154428707 | Common:2; Rare:44 | ||||
| chrX:154486578-154486749 | Rare:28 | ||||
| chrX:154516146-154516537 | Common:4; Rare:80 | ||||
| chrX:154547543-154547693 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chrX:155026527-155026894 | Common:1; Rare:74 | ||||
| chrX:155026903-155027053 | Rare:45 | ||||
| chrX:155071165-155071533 | Rare:84 |