| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:75523245-75523546 | Common:3; Rare:41 | ||||
| chrX:77895367-77895750 | Rare:112; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chrX:78103988-78104361 | Common:4; Rare:133 | ||||
| chrX:79367303-79367587 | Common:1; Rare:56 | ||||
| chrX:81121669-81121863 | Common:2; Rare:30 | ||||
| chrX:81201882-81202250 | Rare:62 | ||||
| chrX:100644125-100644349 | Common:1; Rare:29 | ||||
| chrX:101407893-101408307 | Common:5; Rare:77; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:103585455-103585675 | Common:3; Rare:45 | ||||
| chrX:103607895-103608062 | Rare:30 | ||||
| chrX:103629445-103629527 | Rare:23 | ||||
| chrX:103776630-103776923 | Common:2; Rare:29 | ||||
| chrX:104156888-104157069 | Common:1; Rare:29 | ||||
| chrX:106802528-106802731 | Rare:45 | ||||
| chrX:107118769-107118907 | Common:2; Rare:31 |