| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:63755037-63755431 | Rare:78 | ||||
| chrX:64205667-64206001 | Common:1; Rare:60 | ||||
| chrX:65034698-65034849 | Common:1; Rare:31 | ||||
| chrX:65534706-65534810 | Common:2; Rare:39 | ||||
| chrX:68433328-68433611 | Rare:46 | ||||
| chrX:68498977-68499056 | Rare:18 | ||||
| chrX:68693515-68693679 | Rare:42 | ||||
| chrX:68828837-68829030 | Rare:38 | ||||
| chrX:70289863-70290130 | Rare:48 | ||||
| chrX:71118514-71118748 | Common:1; Rare:47; Clinvar (benign):2 | ||||
| chrX:71283354-71283720 | Rare:56 | ||||
| chrX:71532847-71533128 | Rare:53 | ||||
| chrX:72277186-72277339 | Rare:56 | ||||
| chrX:72305910-72306042 | Rare:27 | ||||
| chrX:73214636-73215009 | Common:1; Rare:55 |