| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:70478807-70479096 | Common:1; Rare:32 | ||||
| chrX:70479340-70479373 | Rare:3 | ||||
| chrX:71254686-71254714 | Rare:4 | ||||
| chrX:71532801-71533115 | Common:1; Rare:66 | ||||
| chrX:75156268-75156369 | Common:2; Rare:26 | ||||
| chrX:76172724-76173141 | Rare:73 | ||||
| chrX:77895386-77895683 | Rare:87; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chrX:77899268-77899545 | Rare:68; Clinvar (benign):1 | ||||
| chrX:78103928-78104380 | Common:4; Rare:165 | ||||
| chrX:81201876-81202199 | Rare:53 | ||||
| chrX:85003736-85003910 | Common:2; Rare:32 | ||||
| chrX:87517651-87518074 | Common:2; Rare:90 | ||||
| chrX:93673538-93673763 | Common:1; Rare:37 | ||||
| chrX:93674210-93674226 | |||||
| chrX:100410221-100410496 | Common:3; Rare:69 |