Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:71068539-71068672 | Rare:59 | ||||
chr2:71130220-71130356 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
chr2:73737300-73737565 | Common:3; Rare:89 | ||||
chr2:74147866-74148140 | Common:1; Rare:69; Clinvar:2 | ||||
chr2:74482919-74483095 | Common:1; Rare:58 | ||||
chr2:74507669-74507775 | Rare:21 | ||||
chr2:74529668-74529888 | Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74958560-74958677 | Common:2; Rare:42 | ||||
chr2:74958874-74959011 | Rare:53 | ||||
chr2:84459204-84459572 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:84905482-84905781 | Common:2; Rare:94 | ||||
chr2:85327936-85328066 | Common:1; Rare:61 | ||||
chr2:85354522-85354775 | Common:1; Rare:83 | ||||
chr2:85595555-85595775 | Common:2; Rare:73 | ||||
chr2:85602657-85602853 | Rare:52 |