| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154371193-154371525 | Common:1; Rare:75; Clinvar:4; Clinvar (benign):6 | ||||
| chrX:154409190-154409453 | Rare:40 | ||||
| chrX:154516146-154516539 | Common:4; Rare:81 | ||||
| chrX:154547553-154547639 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chrX:154762630-154762915 | Common:3; Rare:59; Clinvar:2 | ||||
| chrX:155026722-155026900 | Common:1; Rare:44 | ||||
| chrX:155026907-155027061 | Rare:44 | ||||
| chrX:155071068-155071452 | Common:1; Rare:81 | ||||
| chrX:155612893-155613013 | Common:1; Rare:23 | ||||
| chrY:19744711-19744785 | Rare:1 |