| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:49079858-49079980 | Rare:21 | ||||
| chrX:53422627-53422906 | Common:1; Rare:74 | ||||
| chrX:53686586-53686828 | Common:6; Rare:55 | ||||
| chrX:54530067-54530314 | Common:2; Rare:34 | ||||
| chrX:55000242-55000390 | Rare:34 | ||||
| chrX:55161108-55161321 | Rare:66 | ||||
| chrX:56563514-56563634 | Rare:25; Clinvar:1 | ||||
| chrX:57121422-57121599 | Common:1; Rare:41 | ||||
| chrX:66639025-66639352 | Rare:23 | ||||
| chrX:68498984-68499056 | Rare:16 | ||||
| chrX:70289872-70290131 | Rare:49 | ||||
| chrX:71118462-71118732 | Common:1; Rare:55; Clinvar (benign):2 | ||||
| chrX:75156277-75156313 | Common:1; Rare:9 | ||||
| chrX:75274645-75274702 | Common:1; Rare:10 | ||||
| chrX:77895395-77895741 | Rare:101; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 |