| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154486582-154486880 | Common:1; Rare:58 | ||||
| chrX:154516220-154516485 | Common:2; Rare:43 | ||||
| chrX:154542055-154542247 | Rare:39 | ||||
| chrX:154547550-154547671 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chrX:155071106-155071527 | Common:1; Rare:90 | ||||
| chrY:19744705-19744777 | Rare:1 |