| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153971181-153971341 | Rare:41 | ||||
| chrX:154409205-154409460 | Rare:38 | ||||
| chrX:154428472-154428689 | Common:2; Rare:39 | ||||
| chrX:154516175-154516536 | Common:4; Rare:76 | ||||
| chrX:154547548-154547639 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chrX:154762595-154762958 | Common:4; Rare:86; Clinvar:2 | ||||
| chrX:155026897-155027059 | Rare:45 | ||||
| chrX:155071078-155071520 | Common:1; Rare:95 | ||||
| chrX:155216259-155216507 | Rare:47 | ||||
| chrY:19744711-19744797 | Rare:1 |