Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:71466413-71466738 | Common:6; Rare:81 | ||||
chr2:73214200-73214305 | Common:1; Rare:48 | ||||
chr2:73737276-73737493 | Common:2; Rare:68 | ||||
chr2:73828804-73829029 | Common:1; Rare:53 | ||||
chr2:74147836-74148056 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74421582-74421759 | Rare:62 | ||||
chr2:74465346-74465439 | Rare:26; Clinvar:1 | ||||
chr2:74482908-74483119 | Common:1; Rare:75 | ||||
chr2:74503298-74503475 | Rare:47 | ||||
chr2:74529473-74529997 | Rare:179; Clinvar:5; Clinvar (benign):1 | ||||
chr2:75560858-75561029 | Rare:42 | ||||
chr2:75561258-75561345 | Common:1; Rare:13 | ||||
chr2:75710654-75710779 | Common:2; Rare:48 | ||||
chr2:84459231-84459581 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):4 | ||||
chr2:84905355-84905940 | Common:2; Rare:175 |