| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:56563504-56563707 | Rare:49; Clinvar:1 | ||||
| chrX:56729343-56729562 | Common:1; Rare:27 | ||||
| chrX:57121428-57121686 | Common:1; Rare:61 | ||||
| chrX:64205694-64205999 | Common:1; Rare:55 | ||||
| chrX:65034711-65034857 | Common:1; Rare:32 | ||||
| chrX:65667718-65667810 | Rare:13 | ||||
| chrX:66639017-66639374 | Rare:27 | ||||
| chrX:68498449-68498527 | Rare:11 | ||||
| chrX:68498961-68499101 | Rare:34 | ||||
| chrX:70289845-70290162 | Rare:53 | ||||
| chrX:70290592-70290700 | Rare:19 | ||||
| chrX:71118695-71118760 | Rare:18; Clinvar (benign):2 | ||||
| chrX:71283384-71283736 | Rare:55 | ||||
| chrX:71284206-71284454 | Rare:33 | ||||
| chrX:71301571-71301761 | Common:1; Rare:30 |