| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154490654-154490766 | Common:1; Rare:28 | ||||
| chrX:154516114-154516569 | Common:4; Rare:91 | ||||
| chrX:154547553-154547679 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chrX:155026782-155026935 | Rare:39 | ||||
| chrX:155026949-155027069 | Rare:33 | ||||
| chrX:155071039-155071527 | Common:1; Rare:103 | ||||
| chrY:2935197-2935400 | Common:1 | ||||
| chrY:13479942-13480115 | |||||
| chrY:19744705-19744983 | Rare:3 |