| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120561356-120561734 | Common:1; Rare:64 | ||||
| chrX:120603821-120604156 | Rare:66 | ||||
| chrX:120604636-120604776 | Rare:15 | ||||
| chrX:120629916-120630252 | Common:4; Rare:63 | ||||
| chrX:123732986-123733088 | Rare:23; Clinvar (benign):1 | ||||
| chrX:123859634-123860109 | Common:2; Rare:68 | ||||
| chrX:123860116-123860506 | Common:1; Rare:84 | ||||
| chrX:123960350-123960748 | Rare:28 | ||||
| chrX:123961264-123961435 | Common:2; Rare:22 | ||||
| chrX:123961562-123961855 | Rare:40 | ||||
| chrX:129523198-129523596 | Common:2; Rare:105 | ||||
| chrX:129843800-129844010 | Common:1; Rare:28 | ||||
| chrX:129905921-129906205 | Rare:72 | ||||
| chrX:130165669-130165985 | Rare:68; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130268766-130268998 | Common:1; Rare:70 |