| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154428479-154428695 | Common:2; Rare:39 | ||||
| chrX:154486571-154486760 | Rare:29 | ||||
| chrX:154516165-154516563 | Common:4; Rare:84 | ||||
| chrX:154546798-154546985 | Rare:67 | ||||
| chrX:154547541-154547639 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chrX:155026782-155027069 | Rare:76 | ||||
| chrX:155071068-155071463 | Common:1; Rare:83 |