| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:149939981-149940146 | Common:1; Rare:34 | ||||
| chrX:149944980-149945102 | Common:2; Rare:7 | ||||
| chrX:153694457-153694889 | Common:2; Rare:136; Clinvar:2; Clinvar (benign):26 | ||||
| chrX:154366022-154366369 | Common:3; Rare:104; Clinvar:13; Clinvar (benign):14 | ||||
| chrX:154367639-154367841 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):5 | ||||
| chrY:3002801-3002997 | Rare:1 | ||||
| chrY:19077126-19077191 |