Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:154361726-154362108 | Rare:86; Clinvar:8; Clinvar (benign):7 | ||||
chrX:154367414-154368114 | Common:3; Rare:126; Clinvar:7; Clinvar (benign):18 | ||||
chrX:154369005-154369143 | Rare:27 |