| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154516203-154516539 | Common:3; Rare:64 | ||||
| chrX:154547550-154547639 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chrX:154762585-154762959 | Common:4; Rare:88; Clinvar:2 | ||||
| chrX:155026921-155027050 | Rare:37 |