| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:130110495-130110677 | Common:1; Rare:39 | ||||
| chrX:135344601-135344814 | Common:2; Rare:37 | ||||
| chrX:141177082-141177296 | Rare:26 | ||||
| chrX:152830722-152831112 | Common:2; Rare:68 | ||||
| chrX:153794327-153794672 | Common:1; Rare:109; Clinvar (benign):2 | ||||
| chrX:153934966-153935333 | Common:1; Rare:85 | ||||
| chrX:153972629-153972807 | Common:1; Rare:59 | ||||
| chrX:154019823-154020002 | Rare:32 | ||||
| chrX:154409162-154409442 | Rare:43 | ||||
| chrX:154428466-154428744 | Common:3; Rare:54; Clinvar:1 | ||||
| chrX:154486556-154486833 | Common:1; Rare:49 | ||||
| chrX:154547549-154547661 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chrX:155071068-155071438 | Common:1; Rare:80 |