| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154428446-154428693 | Common:2; Rare:44 | ||||
| chrX:154516124-154516539 | Common:4; Rare:84 | ||||
| chrX:154547553-154547661 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chrX:155026782-155027069 | Rare:76 |