Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:193554847-193555036 | Rare:39 | ||||
chr3:193593091-193593388 | Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
chr3:195543050-195543375 | Common:5; Rare:106 | ||||
chr3:195583878-195584410 | Common:12; Rare:107 | ||||
chr3:195720901-195720986 | Common:1; Rare:17 | ||||
chr3:196227822-196228081 | Common:1; Rare:47 | ||||
chr3:196317798-196317967 | Common:1; Rare:44 | ||||
chr3:196318158-196318368 | Common:1; Rare:89 | ||||
chr3:196432391-196432719 | Common:1; Rare:119 | ||||
chr3:196568520-196568673 | Common:3; Rare:39 | ||||
chr3:196712190-196712348 | Common:2; Rare:56 | ||||
chr3:196867758-196867938 | Rare:61 | ||||
chr3:196942390-196942669 | Common:1; Rare:114 | ||||
chr3:197029780-197029939 | Common:1; Rare:52 | ||||
chr3:197298579-197298687 | Rare:38 |