Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46915734-46915892 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
chr2:47176463-47176569 | Rare:78; Clinvar (benign):3 | ||||
chr2:53786937-53787160 | Rare:90 | ||||
chr2:53971047-53971101 | Common:1; Rare:22 | ||||
chr2:55232412-55232726 | Rare:95 | ||||
chr2:55519409-55519731 | Common:1; Rare:92 | ||||
chr2:58241316-58241404 | Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
chr2:61144916-61145160 | Common:2; Rare:80 | ||||
chr2:63588250-63588541 | Common:1; Rare:84; Clinvar:6 | ||||
chr2:63841767-63841896 | Common:1; Rare:45 | ||||
chr2:69643636-69643845 | Rare:82 | ||||
chr2:70293663-70293900 | Common:3; Rare:76 | ||||
chr2:71130227-71130659 | Common:6; Rare:118; Clinvar:1; Clinvar (benign):2 | ||||
chr2:71276462-71276599 | Rare:41 | ||||
chr2:73828785-73829024 | Common:1; Rare:55 |