Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206085185-206085334 | Rare:53 | ||||
chr2:226796096-226796227 | Rare:46 | ||||
chr2:226796842-226796979 | Rare:41; Clinvar (pathogenic):1 | ||||
chr20:19974490-19974793 | Rare:90; Clinvar (benign):4 | ||||
chr20:50191343-50191410 | Rare:26 | ||||
chr20:50191515-50191678 | Rare:34 | ||||
chr21:44962479-44962798 | Common:1; Rare:49 | ||||
chr22:19878903-19879184 | Common:1; Rare:60 | ||||
chr22:20206309-20206410 | Common:1; Rare:28 | ||||
chr22:20702626-20702874 | Common:3; Rare:59 | ||||
chr22:22297993-22298186 | Common:11; Rare:84 | ||||
chr22:46080124-46080387 | Common:1; Rare:84 | ||||
chr3:37244183-37244287 | Common:2; Rare:30 | ||||
chr3:40453142-40453460 | Common:6; Rare:76 | ||||
chr3:49357221-49357338 | Rare:30 |