| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154412018-154412146 | Common:2; Rare:29; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:154428457-154428695 | Common:2; Rare:41 | ||||
| chrX:154486574-154486772 | Rare:34 | ||||
| chrX:154516140-154516563 | Common:4; Rare:88 | ||||
| chrX:154546788-154546996 | Common:1; Rare:73 | ||||
| chrX:154547553-154547639 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chrX:155026780-155027069 | Rare:78 | ||||
| chrX:155071025-155071527 | Common:2; Rare:105 |