| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:104112395-104112668 | Rare:62 | ||||
| chrX:104156894-104157069 | Common:1; Rare:29 | ||||
| chrX:106802439-106802778 | Common:1; Rare:61 | ||||
| chrX:107118581-107118889 | Common:3; Rare:57 | ||||
| chrX:107206410-107206653 | Common:1; Rare:39 | ||||
| chrX:107716524-107716842 | Common:1; Rare:60 | ||||
| chrX:108091500-108091822 | Rare:87 | ||||
| chrX:108439457-108439882 | Common:3; Rare:96 | ||||
| chrX:109537034-109537254 | Common:2; Rare:55 | ||||
| chrX:110318077-110318248 | Rare:41 | ||||
| chrX:111096010-111096362 | Common:1; Rare:51 | ||||
| chrX:111680984-111681319 | Rare:86; Clinvar (benign):7 | ||||
| chrX:111681552-111681705 | Rare:58 | ||||
| chrX:112840588-112840634 | Rare:8 | ||||
| chrX:112840775-112841033 | Rare:54 |