| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71118433-71118770 | Common:1; Rare:62; Clinvar (benign):2 | ||||
| chrX:71254111-71254354 | Common:1; Rare:40 | ||||
| chrX:71254687-71254846 | Common:1; Rare:15 | ||||
| chrX:71255100-71255540 | Rare:48 | ||||
| chrX:71282777-71283177 | Common:2; Rare:74 | ||||
| chrX:71283308-71283714 | Rare:62 | ||||
| chrX:71284003-71284165 | Common:1; Rare:18 | ||||
| chrX:71365858-71366239 | Common:4; Rare:74 | ||||
| chrX:71532834-71533133 | Rare:60 | ||||
| chrX:71534146-71534504 | Common:1; Rare:55 | ||||
| chrX:71910629-71910874 | Common:1; Rare:36 | ||||
| chrX:71911218-71911735 | Common:1; Rare:166 | ||||
| chrX:72131917-72132197 | Common:1; Rare:65 | ||||
| chrX:72181286-72181559 | Common:4; Rare:72 | ||||
| chrX:72239011-72239171 | Common:1; Rare:38 |