| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120561370-120561691 | Common:1; Rare:52 | ||||
| chrX:120603797-120604147 | Rare:64 | ||||
| chrX:120629938-120630238 | Common:4; Rare:57 | ||||
| chrX:123960413-123960725 | Rare:20 | ||||
| chrX:123961225-123961432 | Common:2; Rare:28 | ||||
| chrX:123961540-123961843 | Rare:43 | ||||
| chrX:129523381-129523641 | Common:4; Rare:49 | ||||
| chrX:129843808-129844026 | Rare:26 | ||||
| chrX:129906080-129906195 | Rare:25 | ||||
| chrX:130401871-130402029 | Common:2; Rare:50 | ||||
| chrX:132023136-132023336 | Rare:50 | ||||
| chrX:133985490-133985808 | Rare:60 | ||||
| chrX:134237102-134237305 | Rare:46 | ||||
| chrX:134373143-134373519 | Common:4; Rare:76; Clinvar (benign):1 | ||||
| chrX:134460055-134460205 | Common:3; Rare:37 |