| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119852942-119853231 | Common:3; Rare:48; Clinvar (benign):2 | ||||
| chrX:119871622-119871923 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chrX:120560908-120561210 | Rare:64 | ||||
| chrX:120561428-120561622 | Common:1; Rare:29 | ||||
| chrX:120603825-120604154 | Rare:65 | ||||
| chrX:120629916-120630261 | Common:4; Rare:67 | ||||
| chrX:123859974-123860272 | Rare:53 | ||||
| chrX:123961252-123961432 | Common:2; Rare:24 | ||||
| chrX:123961532-123961828 | Rare:41 | ||||
| chrX:129905981-129906201 | Rare:60 | ||||
| chrX:130165703-130165961 | Rare:54; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130339756-130339971 | Rare:38 | ||||
| chrX:130401936-130402031 | Common:2; Rare:32 | ||||
| chrX:131579037-131579244 | Common:1; Rare:52 | ||||
| chrX:132022943-132023336 | Rare:83 |