Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:57227604-57227919 | Common:3; Rare:106 | ||||
chr3:57556006-57556314 | Rare:72 | ||||
chr3:57597333-57597661 | Common:4; Rare:104 | ||||
chr3:57889883-57890092 | Rare:46; Clinvar (benign):2 | ||||
chr3:58433811-58433975 | Common:1; Rare:65; Clinvar (benign):2 | ||||
chr3:62318932-62319068 | Rare:52 | ||||
chr3:63863777-63864132 | Common:7; Rare:118 | ||||
chr3:67654572-67654727 | Common:1; Rare:60 | ||||
chr3:69013208-69013373 | Rare:47 | ||||
chr3:69013601-69013921 | Common:1; Rare:109 | ||||
chr3:71130553-71130685 | Rare:54; Clinvar:1 | ||||
chr3:88058926-88059294 | Common:3; Rare:135 | ||||
chr3:88149654-88150009 | Rare:91 | ||||
chr3:94028590-94028727 | Rare:25 | ||||
chr3:94062930-94063011 | Rare:27 |