| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:65034693-65034823 | Common:1; Rare:27 | ||||
| chrX:65667538-65667808 | Rare:47 | ||||
| chrX:68498941-68499056 | Rare:24 | ||||
| chrX:70289888-70289987 | Rare:24 | ||||
| chrX:70478951-70479089 | Rare:16 | ||||
| chrX:71254681-71254739 | Common:1; Rare:7 | ||||
| chrX:71365937-71366238 | Common:3; Rare:57 | ||||
| chrX:71532801-71533145 | Common:1; Rare:72 | ||||
| chrX:74614433-74614856 | Common:1; Rare:95 | ||||
| chrX:75274645-75274702 | Common:1; Rare:10 | ||||
| chrX:75523009-75523212 | Common:1; Rare:42 | ||||
| chrX:75523219-75523543 | Common:3; Rare:48 | ||||
| chrX:77895412-77895750 | Rare:93; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:80809863-80810151 | Rare:36 | ||||
| chrX:81201881-81202197 | Rare:53 |