| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107716419-107716981 | Common:2; Rare:92 | ||||
| chrX:107716983-107717209 | Common:1; Rare:27 | ||||
| chrX:107775600-107775890 | Rare:50 | ||||
| chrX:107775918-107775950 | Rare:5 | ||||
| chrX:108091500-108091835 | Rare:89 | ||||
| chrX:108439479-108439901 | Common:3; Rare:93 | ||||
| chrX:109733164-109733436 | Common:1; Rare:61 | ||||
| chrX:110318075-110318251 | Rare:44 | ||||
| chrX:110795760-110795873 | Rare:13 | ||||
| chrX:111681155-111681302 | Rare:45; Clinvar (benign):7 | ||||
| chrX:115560988-115561237 | Common:1; Rare:45 | ||||
| chrX:118116735-118116944 | Common:1; Rare:34 | ||||
| chrX:118345803-118346155 | Common:4; Rare:64 | ||||
| chrX:119468216-119468506 | Common:3; Rare:97 | ||||
| chrX:119469078-119469273 | Rare:58 |