| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107716929-107717185 | Common:2; Rare:31 | ||||
| chrX:107775567-107775959 | Rare:65 | ||||
| chrX:107825759-107825876 | Rare:10 | ||||
| chrX:108091504-108091822 | Rare:86 | ||||
| chrX:108438413-108438584 | Rare:20 | ||||
| chrX:108439445-108440013 | Common:3; Rare:120 | ||||
| chrX:108735708-108736009 | Rare:70 | ||||
| chrX:108736021-108736045 | Rare:5 | ||||
| chrX:108736446-108736564 | Rare:16 | ||||
| chrX:109537065-109537237 | Common:1; Rare:36 | ||||
| chrX:109733158-109733479 | Common:1; Rare:75 | ||||
| chrX:110317898-110318286 | Rare:104 | ||||
| chrX:111681028-111681302 | Rare:70; Clinvar (benign):7 | ||||
| chrX:112840822-112841024 | Rare:43 | ||||
| chrX:115560819-115561243 | Common:2; Rare:66 |