| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120561070-120561137 | Rare:10 | ||||
| chrX:120561376-120561724 | Common:1; Rare:55 | ||||
| chrX:120603907-120604175 | Rare:54 | ||||
| chrX:120604580-120604769 | Rare:22 | ||||
| chrX:120629916-120630332 | Common:4; Rare:82 | ||||
| chrX:123733010-123733152 | Rare:21 | ||||
| chrX:123860341-123860454 | Common:1; Rare:25 | ||||
| chrX:123960350-123960711 | Rare:26 | ||||
| chrX:123961264-123961434 | Common:2; Rare:22 | ||||
| chrX:123961506-123961856 | Rare:48 | ||||
| chrX:129779826-129780002 | Rare:28 | ||||
| chrX:129905941-129906212 | Rare:70 | ||||
| chrX:130165658-130165908 | Rare:51; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130171862-130172015 | Common:1; Rare:41 | ||||
| chrX:130401881-130402061 | Common:2; Rare:50 |