| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:149540409-149541071 | Common:7; Rare:106 | ||||
| chrX:149938414-149938635 | Common:1; Rare:57 | ||||
| chrX:151396901-151397253 | Common:5; Rare:150 | ||||
| chrX:152830712-152831103 | Common:2; Rare:69 | ||||
| chrX:153599100-153599313 | Common:12; Rare:41 | ||||
| chrX:153794310-153794667 | Common:1; Rare:112; Clinvar (benign):2 | ||||
| chrX:153934977-153935333 | Common:1; Rare:80 | ||||
| chrX:153971173-153971296 | Rare:29 | ||||
| chrX:153971736-153971944 | Rare:53 | ||||
| chrX:154398794-154398936 | Common:3; Rare:31 | ||||
| chrX:154409198-154409462 | Rare:38 | ||||
| chrX:154411384-154411603 | Rare:42 | ||||
| chrX:154428466-154428773 | Common:3; Rare:62; Clinvar:1 | ||||
| chrX:154486571-154486798 | Rare:41 | ||||
| chrX:154490626-154490785 | Common:2; Rare:43 |