Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37506629-37506948 | Rare:66 | ||||
chr19:37551297-37551447 | Rare:39 | ||||
chr19:37594739-37594892 | Rare:42 | ||||
chr19:37655409-37655549 | Common:2; Rare:53 | ||||
chr19:37719693-37719791 | Rare:39 | ||||
chr19:37779579-37779662 | Rare:18 | ||||
chr19:37907045-37907284 | Rare:52 | ||||
chr19:38224138-38224353 | Rare:66 | ||||
chr19:38336308-38336472 | Common:1; Rare:34 | ||||
chr19:38374427-38374829 | Rare:158 | ||||
chr19:38618923-38619252 | Common:3; Rare:100 | ||||
chr19:38647378-38647733 | Common:3; Rare:128 | ||||
chr19:38852324-38852625 | Rare:72 | ||||
chr19:38899581-38899954 | Rare:101 | ||||
chr19:38930742-38930992 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):3 |