| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:44283479-44283725 | Common:1; Rare:36 | ||||
| chrX:45615454-45615750 | Rare:56 | ||||
| chrX:45851527-45851640 | Common:1; Rare:22 | ||||
| chrX:47129173-47129353 | Common:1; Rare:27 | ||||
| chrX:47198873-47199080 | Rare:50; Clinvar (benign):2 | ||||
| chrX:47212757-47213080 | Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:47224453-47224693 | Common:1; Rare:38 | ||||
| chrX:48741944-48742155 | Rare:34 | ||||
| chrX:51325669-51325815 | Rare:22 | ||||
| chrX:51505879-51506060 | Common:2; Rare:26 | ||||
| chrX:51743950-51744081 | Common:1; Rare:18 | ||||
| chrX:52261843-52261954 | Rare:21 | ||||
| chrX:52935081-52935237 | Common:1; Rare:46 | ||||
| chrX:53088471-53088836 | Common:3; Rare:101 | ||||
| chrX:53093879-53094232 | Rare:64 |