| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103685579-103685815 | Common:1; Rare:27 | ||||
| chrX:103685979-103686134 | Rare:24 | ||||
| chrX:103686590-103687046 | Common:4; Rare:61 | ||||
| chrX:103919045-103919166 | Common:4; Rare:27 | ||||
| chrX:104156922-104157073 | Common:1; Rare:28 | ||||
| chrX:106802491-106802787 | Common:1; Rare:57 | ||||
| chrX:106802848-106802975 | Rare:34 | ||||
| chrX:107118775-107118894 | Common:2; Rare:26 | ||||
| chrX:107628280-107628727 | Common:1; Rare:62; Clinvar (benign):2 | ||||
| chrX:108091410-108091822 | Rare:107 | ||||
| chrX:108439457-108439889 | Common:3; Rare:98 | ||||
| chrX:108439920-108439946 | Rare:2 | ||||
| chrX:109733141-109733598 | Common:1; Rare:105 | ||||
| chrX:110002784-110003153 | Common:2; Rare:65 | ||||
| chrX:110317865-110318231 | Rare:96 |