| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154516130-154516537 | Common:4; Rare:83 | ||||
| chrX:154532655-154533131 | Common:2; Rare:114; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chrX:154534042-154534408 | Common:1; Rare:91; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chrX:154547550-154547660 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chrX:154762626-154762977 | Common:3; Rare:78; Clinvar:2 | ||||
| chrX:155026683-155026951 | Common:1; Rare:66 |