| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71283386-71283720 | Rare:54 | ||||
| chrX:71365907-71366256 | Common:4; Rare:63 | ||||
| chrX:71532866-71533152 | Rare:54 | ||||
| chrX:72068967-72069248 | Rare:44 | ||||
| chrX:72181302-72181323 | Rare:5 | ||||
| chrX:72714238-72714334 | Rare:20 | ||||
| chrX:73214265-73214566 | Common:4; Rare:85 | ||||
| chrX:73214575-73215004 | Common:1; Rare:63 | ||||
| chrX:73563060-73563324 | Common:1; Rare:34 | ||||
| chrX:74421309-74421530 | Rare:50; Clinvar (benign):1 | ||||
| chrX:74614214-74614331 | Rare:21 | ||||
| chrX:74614433-74614725 | Rare:53 | ||||
| chrX:74925270-74925570 | Common:1; Rare:43 | ||||
| chrX:75156018-75156393 | Common:3; Rare:100; Clinvar (benign):2 | ||||
| chrX:75274578-75274737 | Common:2; Rare:29 |