| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153794089-153794237 | Common:2; Rare:27 | ||||
| chrX:153794316-153794668 | Common:1; Rare:113; Clinvar (benign):2 | ||||
| chrX:153934966-153935342 | Common:1; Rare:91 | ||||
| chrX:154019831-154020017 | Rare:37 | ||||
| chrX:154398835-154398992 | Common:2; Rare:31 | ||||
| chrX:154428466-154428794 | Common:3; Rare:67; Clinvar:1 | ||||
| chrX:154486568-154486799 | Rare:41 | ||||
| chrX:154516114-154516479 | Common:3; Rare:67 | ||||
| chrX:154532799-154533021 | Rare:60; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chrX:154547530-154547660 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chrX:155071068-155071525 | Common:1; Rare:100 |