Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:103356992-103357139 | Rare:23 | ||||
chrX:134549639-134549822 | Common:1; Rare:42 | ||||
chrX:151878771-151878952 | Common:1; Rare:32 | ||||
chrX:154362268-154362537 | Common:1; Rare:77; Clinvar:10; Clinvar (benign):7 |