| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120561367-120561568 | Common:1; Rare:39 | ||||
| chrX:120603796-120604347 | Rare:100 | ||||
| chrX:120604560-120604866 | Rare:38 | ||||
| chrX:123613203-123613467 | Common:2; Rare:39 | ||||
| chrX:123732957-123733197 | Rare:44; Clinvar (benign):1 | ||||
| chrX:123859632-123859883 | Common:1; Rare:35 | ||||
| chrX:123860642-123860830 | Rare:23 | ||||
| chrX:123960595-123960907 | Rare:33 | ||||
| chrX:123961263-123961354 | Common:2; Rare:18 | ||||
| chrX:123961540-123961847 | Rare:44 | ||||
| chrX:123961953-123962116 | Rare:25 | ||||
| chrX:123963071-123963444 | Common:1; Rare:47 | ||||
| chrX:123963492-123963536 | Rare:7 | ||||
| chrX:129523198-129523305 | Rare:37 | ||||
| chrX:129540110-129540339 | Common:3; Rare:40 |