| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154546801-154546996 | Rare:70 | ||||
| chrX:154547553-154547639 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chrX:155071101-155071452 | Common:1; Rare:75 | ||||
| chrX:155216266-155216480 | Rare:37 |