| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:138711652-138711925 | Common:2; Rare:51 | ||||
| chrX:141177070-141177314 | Common:1; Rare:31 | ||||
| chrX:150898596-150898911 | Common:3; Rare:90 | ||||
| chrX:150983037-150983373 | Common:3; Rare:68 | ||||
| chrX:151397054-151397257 | Common:4; Rare:102 | ||||
| chrX:152830712-152831095 | Common:2; Rare:67 | ||||
| chrX:153599102-153599351 | Common:13; Rare:52 | ||||
| chrX:153724361-153724613 | Common:2; Rare:61 | ||||
| chrX:153794322-153794682 | Common:1; Rare:110; Clinvar (benign):2 | ||||
| chrX:154486582-154486767 | Rare:33 | ||||
| chrX:154516187-154516503 | Common:3; Rare:64 | ||||
| chrX:154547553-154547639 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chrX:155027020-155027055 | Rare:13 | ||||
| chrX:155071121-155071520 | Common:1; Rare:85 | ||||
| chrX:155216272-155216488 | Rare:37 |