Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:36288725-36289194 | Common:2; Rare:139; Clinvar:4; Clinvar (benign):7 | ||||
chr22:36328041-36328297 | Common:1; Rare:60 | ||||
chr22:36331578-36331738 | Common:2; Rare:27 | ||||
chr22:38741007-38741270 | Common:1; Rare:55 | ||||
chr22:41197424-41197621 | Common:1; Rare:46 | ||||
chr22:41413835-41414039 | Common:2; Rare:55 | ||||
chr22:41447577-41447834 | Common:1; Rare:91 | ||||
chr22:41522671-41523272 | Rare:154; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr22:41529282-41529387 | Rare:33 | ||||
chr22:46044776-46044981 | Common:1; Rare:50 | ||||
chr22:46069860-46070056 | Rare:43 | ||||
chr3:9396625-9396705 | Rare:34 | ||||
chr3:12587607-12587862 | Common:1; Rare:44 | ||||
chr3:12662743-12662892 | Rare:35 | ||||
chr3:12994102-12994408 | Common:2; Rare:67 |