| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119852891-119853237 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):3 | ||||
| chrX:119871574-119872013 | Common:3; Rare:85; Clinvar (benign):4 | ||||
| chrX:119943482-119943852 | Rare:87 | ||||
| chrX:120560917-120561137 | Rare:45 | ||||
| chrX:120561365-120561715 | Common:1; Rare:55 | ||||
| chrX:120603903-120604154 | Rare:50 | ||||
| chrX:120629932-120630266 | Common:4; Rare:64 | ||||
| chrX:123733011-123733189 | Rare:32 | ||||
| chrX:123859634-123860506 | Common:3; Rare:153 | ||||
| chrX:123960205-123960919 | Common:1; Rare:83 | ||||
| chrX:123961281-123961435 | Common:2; Rare:21 | ||||
| chrX:123961506-123961856 | Rare:48 | ||||
| chrX:123962767-123962885 | Rare:11 | ||||
| chrX:123963062-123963160 | Rare:10 | ||||
| chrX:123963204-123963303 | Rare:14 |