| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154534038-154534525 | Common:2; Rare:117; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
| chrX:154541909-154542273 | Rare:59 | ||||
| chrX:154547221-154547429 | Rare:42 | ||||
| chrX:154547530-154547893 | Common:2; Rare:70; Clinvar (benign):1 | ||||
| chrX:154762800-154762975 | Rare:46; Clinvar:2 | ||||
| chrX:154781788-154781829 | Rare:10 | ||||
| chrX:155026753-155027061 | Rare:83 | ||||
| chrX:155070809-155070853 | Rare:4 |