| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961562-123961862 | Rare:41 | ||||
| chrX:129523195-129523636 | Common:4; Rare:109 | ||||
| chrX:129540231-129540398 | Common:1; Rare:37 | ||||
| chrX:129779817-129779903 | Rare:9 | ||||
| chrX:129779912-129779989 | Rare:14 | ||||
| chrX:129905962-129906213 | Rare:65 | ||||
| chrX:130110452-130110623 | Rare:39 | ||||
| chrX:130165664-130165908 | Rare:49; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130171789-130172009 | Common:1; Rare:53 | ||||
| chrX:130339659-130339976 | Rare:52 | ||||
| chrX:130401884-130402059 | Common:2; Rare:48 | ||||
| chrX:132218019-132218291 | Rare:32 | ||||
| chrX:132219438-132219611 | Rare:21 | ||||
| chrX:132488870-132488990 | Rare:35 | ||||
| chrX:132489864-132490076 | Common:1; Rare:50 |