| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:150568343-150568653 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chrX:150898520-150898845 | Common:3; Rare:87 | ||||
| chrX:151397054-151397276 | Common:4; Rare:112 | ||||
| chrX:152830712-152831050 | Common:1; Rare:63 | ||||
| chrX:153599057-153599357 | Common:13; Rare:59 | ||||
| chrX:153724341-153724867 | Common:3; Rare:124 | ||||
| chrX:153780910-153781063 | Common:1; Rare:50 | ||||
| chrX:153794268-153794709 | Common:1; Rare:137; Clinvar (benign):2 | ||||
| chrX:153971174-153971316 | Rare:36 | ||||
| chrX:153972433-153972783 | Common:1; Rare:108 | ||||
| chrX:154409159-154409469 | Rare:45 | ||||
| chrX:154412036-154412074 | Common:1; Rare:12; Clinvar (benign):1 | ||||
| chrX:154428467-154428695 | Common:2; Rare:40 | ||||
| chrX:154444049-154444343 | Common:6; Rare:67 | ||||
| chrX:154486559-154486798 | Rare:41 |