| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:130165689-130165908 | Rare:44; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132023160-132023276 | Rare:32 | ||||
| chrX:149505239-149505470 | Rare:65 | ||||
| chrX:149938440-149938632 | Common:1; Rare:50 | ||||
| chrX:151397057-151397278 | Common:4; Rare:112 | ||||
| chrX:151974674-151974925 | Common:1; Rare:69 | ||||
| chrX:152733725-152733801 | Rare:29 | ||||
| chrX:152830712-152831099 | Common:2; Rare:67 | ||||
| chrX:153599099-153599350 | Common:13; Rare:52 | ||||
| chrX:153794316-153794684 | Common:1; Rare:113; Clinvar (benign):2 | ||||
| chrX:153971180-153971331 | Rare:37 | ||||
| chrX:153972440-153972782 | Common:1; Rare:104 | ||||
| chrX:154428487-154428687 | Common:2; Rare:37 | ||||
| chrX:154478779-154479037 | Common:4; Rare:75 | ||||
| chrX:154516161-154516537 | Common:4; Rare:79 |