| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:149938402-149938677 | Common:2; Rare:69 | ||||
| chrX:150568896-150569076 | Rare:31 | ||||
| chrX:150898569-150898887 | Common:2; Rare:91 | ||||
| chrX:151397062-151397257 | Common:4; Rare:98 | ||||
| chrX:151974655-151974775 | Rare:39 | ||||
| chrX:152830712-152831100 | Common:2; Rare:69 | ||||
| chrX:152941534-152941701 | Common:1; Rare:39 | ||||
| chrX:153599069-153599351 | Common:13; Rare:56 | ||||
| chrX:153723191-153723506 | Common:1; Rare:58 | ||||
| chrX:153724083-153724290 | Rare:32 | ||||
| chrX:153724332-153724867 | Common:3; Rare:124 | ||||
| chrX:153780941-153781041 | Rare:25 | ||||
| chrX:153786804-153787078 | Rare:60 | ||||
| chrX:153794073-153794236 | Common:2; Rare:27 | ||||
| chrX:153794286-153794690 | Common:1; Rare:124; Clinvar (benign):2 |