| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120560870-120561161 | Rare:90 | ||||
| chrX:120561310-120561800 | Common:4; Rare:143 | ||||
| chrX:120603797-120604025 | Rare:80 | ||||
| chrX:120604027-120604158 | Rare:28 | ||||
| chrX:120629932-120630325 | Common:4; Rare:76 | ||||
| chrX:123732992-123733189 | Rare:76; Clinvar (benign):2 | ||||
| chrX:123859904-123860446 | Common:1; Rare:162 | ||||
| chrX:123960270-123960884 | Rare:101 | ||||
| chrX:123961180-123961450 | Common:4; Rare:62 | ||||
| chrX:123961495-123962105 | Rare:160 | ||||
| chrX:123963000-123963520 | Common:3; Rare:129 | ||||
| chrX:129843729-129844069 | Common:2; Rare:76 | ||||
| chrX:129905914-129906209 | Rare:104 | ||||
| chrX:129982314-129982663 | Common:2; Rare:90 | ||||
| chrX:130110460-130110674 | Common:1; Rare:81 |