| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154516114-154516565 | Common:4; Rare:91 | ||||
| chrX:154546801-154546980 | Rare:65 | ||||
| chrX:154547553-154547660 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chrX:154762585-154762922 | Common:4; Rare:74; Clinvar:2 | ||||
| chrX:155026787-155027069 | Rare:76 | ||||
| chrX:155071045-155071533 | Common:1; Rare:103 | ||||
| chrX:155881196-155881424 | Common:3; Rare:66 | ||||
| chrY:2935266-2935400 | |||||
| chrY:19744712-19745038 | Rare:3 |