| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:68433830-68434107 | Common:2; Rare:34 | ||||
| chrX:68498961-68499081 | Rare:28 | ||||
| chrX:68828837-68829053 | Common:1; Rare:42 | ||||
| chrX:70289872-70290122 | Rare:47 | ||||
| chrX:71254691-71254751 | Common:1; Rare:7 | ||||
| chrX:72238997-72239118 | Rare:29 | ||||
| chrX:74614574-74614833 | Common:1; Rare:60 | ||||
| chrX:75156245-75156369 | Common:2; Rare:39 | ||||
| chrX:75274651-75274702 | Rare:10 | ||||
| chrX:75523018-75523206 | Common:1; Rare:39 | ||||
| chrX:76172984-76173165 | Rare:47 | ||||
| chrX:77895417-77895750 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:77899246-77899505 | Rare:61 | ||||
| chrX:78103939-78104400 | Common:4; Rare:164 | ||||
| chrX:78139612-78139804 | Common:2; Rare:79 |