Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:51366878-51367107 | Common:1; Rare:47 | ||||
chr19:52028398-52028599 | Common:1; Rare:34 | ||||
chr19:52397719-52397877 | Common:3; Rare:45 | ||||
chr19:52690484-52690656 | Common:4; Rare:43 | ||||
chr19:54115271-54115421 | Common:1; Rare:34; Clinvar (benign):1 | ||||
chr19:54115612-54115795 | Common:2; Rare:46; Clinvar:5 | ||||
chr19:54449012-54449244 | Common:3; Rare:66 | ||||
chr19:55643448-55643652 | Common:3; Rare:64 | ||||
chr19:55675063-55675333 | Common:3; Rare:126 | ||||
chr19:58002728-58002917 | Common:2; Rare:102 | ||||
chr19:58326875-58327019 | Common:1; Rare:30 | ||||
chr19:58347605-58347798 | Common:8; Rare:90 | ||||
chr19:58499228-58499524 | Common:1; Rare:88; Clinvar:2 | ||||
chr19:58544539-58544761 | Rare:92 | ||||
chr2:3519516-3519660 | Common:1; Rare:37 |