Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46521480-46521526 | Rare:9 | ||||
chr2:47803174-47803455 | Common:1; Rare:98; Clinvar:10; Clinvar (benign):12 | ||||
chr2:47906476-47906823 | Common:2; Rare:124 | ||||
chr2:48479243-48479482 | Rare:65 | ||||
chr2:48510432-48510666 | Common:2; Rare:45 | ||||
chr2:55223252-55223522 | Common:3; Rare:92 | ||||
chr2:55282203-55282362 | Common:5; Rare:54 | ||||
chr2:61471270-61471386 | Common:2; Rare:44 | ||||
chr2:62724232-62724500 | Rare:36 | ||||
chr2:65090984-65091182 | Rare:27 | ||||
chr2:66432020-66432169 | Rare:32 | ||||
chr2:66581625-66581906 | Common:5; Rare:76 | ||||
chr2:70086269-70086485 | Common:4; Rare:86 | ||||
chr2:71454445-71454731 | Rare:55 | ||||
chr2:73833052-73833299 | Common:1; Rare:47 |