| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:70289875-70290099 | Rare:42 | ||||
| chrX:71215039-71215286 | Common:1; Rare:26 | ||||
| chrX:71254677-71254736 | Common:1; Rare:7 | ||||
| chrX:71365940-71366250 | Common:3; Rare:57 | ||||
| chrX:71532859-71533161 | Rare:59 | ||||
| chrX:72181556-72181796 | Common:2; Rare:65 | ||||
| chrX:72714234-72714357 | Common:1; Rare:31 | ||||
| chrX:75156018-75156036 | Rare:3 | ||||
| chrX:75156268-75156369 | Common:2; Rare:26 | ||||
| chrX:75274651-75274702 | Rare:10 | ||||
| chrX:75523009-75523134 | Rare:29 | ||||
| chrX:77895355-77895750 | Rare:116; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chrX:77899256-77899590 | Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:78103951-78104361 | Common:4; Rare:151 | ||||
| chrX:81201884-81202199 | Rare:53 |