| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:65034705-65034863 | Common:1; Rare:34 | ||||
| chrX:68498984-68499059 | Rare:16 | ||||
| chrX:71111394-71111755 | Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chrX:71254108-71254238 | Common:1; Rare:21 | ||||
| chrX:71283424-71283724 | Rare:48 | ||||
| chrX:72273675-72273840 | Rare:32 | ||||
| chrX:73563389-73563494 | Rare:43 | ||||
| chrX:75274640-75274708 | Common:1; Rare:13 | ||||
| chrX:76172943-76173151 | Rare:49 | ||||
| chrX:77895398-77895767 | Common:1; Rare:107; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:77899269-77899533 | Rare:65; Clinvar (benign):1 | ||||
| chrX:78327439-78327632 | Rare:25 | ||||
| chrX:78945227-78945459 | Rare:27 | ||||
| chrX:80809863-80810155 | Rare:36 | ||||
| chrX:81201911-81202158 | Rare:44 |