| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154490605-154490804 | Common:2; Rare:49 | ||||
| chrX:154516077-154516499 | Common:4; Rare:81 | ||||
| chrX:154532702-154533163 | Common:2; Rare:113; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chrX:154534052-154534390 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chrX:154547530-154547660 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chrX:154762535-154762977 | Common:4; Rare:100; Clinvar:2 | ||||
| chrX:154773029-154773254 | Rare:34; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chrX:154805330-154805586 | Rare:48 | ||||
| chrX:155026782-155027069 | Rare:76 |