| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103356247-103356603 | Common:4; Rare:49 | ||||
| chrX:103376441-103376607 | Common:1; Rare:24 | ||||
| chrX:103585455-103585677 | Common:3; Rare:45 | ||||
| chrX:103628682-103628998 | Common:1; Rare:40 | ||||
| chrX:103629437-103629527 | Common:1; Rare:26 | ||||
| chrX:103776705-103776932 | Common:2; Rare:23 | ||||
| chrX:103919057-103919189 | Common:3; Rare:29 | ||||
| chrX:104156891-104157069 | Common:1; Rare:29 | ||||
| chrX:107118769-107118899 | Common:2; Rare:28 | ||||
| chrX:107628179-107628531 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chrX:107716432-107716838 | Common:1; Rare:69 | ||||
| chrX:108091516-108091829 | Rare:83 | ||||
| chrX:108439457-108440030 | Common:3; Rare:122 | ||||
| chrX:110317917-110318297 | Rare:103 | ||||
| chrX:112840822-112840951 | Rare:28 |