Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:69084808-69085219 | Common:3; Rare:109 | ||||
chr3:71130539-71130672 | Rare:49; Clinvar:2 | ||||
chr3:81761510-81761800 | Common:8; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
chr3:88058935-88059279 | Common:2; Rare:118 | ||||
chr3:88149628-88150033 | Common:2; Rare:111 | ||||
chr3:93979922-93980201 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
chr3:94062914-94063011 | Rare:29 | ||||
chr3:97764491-97764804 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
chr3:98522855-98523150 | Common:1; Rare:88 | ||||
chr3:99638385-99638624 | Common:1; Rare:57 | ||||
chr3:99817568-99817928 | Rare:107 | ||||
chr3:99876129-99876254 | Rare:31 | ||||
chr3:100260699-100261021 | Rare:86 | ||||
chr3:100401407-100401602 | Common:1; Rare:33 | ||||
chr3:100492413-100492688 | Common:2; Rare:90 |