| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153599102-153599369 | Common:13; Rare:54 | ||||
| chrX:153724570-153724878 | Common:1; Rare:65 | ||||
| chrX:153794301-153794693 | Common:1; Rare:117; Clinvar (benign):2 | ||||
| chrX:153934966-153935333 | Common:1; Rare:85 | ||||
| chrX:153971168-153971307 | Rare:34 | ||||
| chrX:153972442-153972782 | Common:1; Rare:104 | ||||
| chrX:154409196-154409427 | Rare:35 | ||||
| chrX:154428461-154428689 | Common:2; Rare:39 | ||||
| chrX:154478764-154479062 | Common:4; Rare:87 | ||||
| chrX:154486571-154486798 | Rare:41 | ||||
| chrX:154490654-154490815 | Common:1; Rare:38 | ||||
| chrX:154516152-154516537 | Common:4; Rare:80 | ||||
| chrX:154547550-154547639 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chrX:155026680-155027061 | Common:1; Rare:98 | ||||
| chrX:155071078-155071479 | Common:1; Rare:82 |