| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153724584-153724861 | Common:1; Rare:59 | ||||
| chrX:153794319-153794667 | Common:1; Rare:112; Clinvar (benign):2 | ||||
| chrX:153926203-153926468 | Common:3; Rare:58 | ||||
| chrX:153934966-153935343 | Common:1; Rare:91 | ||||
| chrX:154379624-154380050 | Common:1; Rare:112; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chrX:154398794-154399006 | Common:4; Rare:47 | ||||
| chrX:154411437-154411558 | Rare:19 | ||||
| chrX:154428472-154428689 | Common:2; Rare:39 | ||||
| chrX:154486547-154486772 | Rare:34 | ||||
| chrX:154490627-154490870 | Common:2; Rare:57 | ||||
| chrX:154516175-154516504 | Common:4; Rare:69 | ||||
| chrX:154547550-154547660 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chrX:155026683-155026953 | Common:1; Rare:67 | ||||
| chrX:155071068-155071520 | Common:1; Rare:97 |