| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154532769-154533039 | Rare:70; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chrX:154541948-154542273 | Rare:54 | ||||
| chrX:154547541-154547879 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chrX:155071106-155071533 | Common:1; Rare:90 | ||||
| chrY:13479942-13480060 | |||||
| chrY:19744705-19744797 | Rare:1 | ||||
| chrY:19744882-19744972 | Rare:1 |