| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:110509774-110509924 | Common:1; Rare:25 | ||||
| chrX:110667670-110668030 | Rare:50 | ||||
| chrX:110964700-110965220 | Common:1; Rare:74 | ||||
| chrX:111372200-111372403 | Common:1; Rare:30 | ||||
| chrX:111377140-111377540 | Rare:41 | ||||
| chrX:111409902-111410302 | Rare:60; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chrX:111511591-111511991 | Common:2; Rare:78 | ||||
| chrX:111519220-111519520 | Common:2; Rare:41 | ||||
| chrX:112704110-112704480 | Common:1; Rare:41 | ||||
| chrX:112834007-112834407 | Common:1; Rare:73 | ||||
| chrX:112837980-112838350 | Common:1; Rare:56 | ||||
| chrX:112839054-112839454 | Rare:60 | ||||
| chrX:115344795-115345640 | Common:7; Rare:197 | ||||
| chrX:115562700-115562930 | Common:1; Rare:25 | ||||
| chrX:115968514-115968627 | Rare:15 |