Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:4792674-4793073 | Common:2; Rare:150 | ||||
chr9:5437809-5437995 | Common:1; Rare:64 | ||||
chr9:5450430-5450577 | Common:5; Rare:52 | ||||
chr9:5628984-5629203 | Common:1; Rare:106 | ||||
chr9:6015591-6015732 | Rare:64 | ||||
chr9:15422709-15422898 | Rare:80 | ||||
chr9:19049337-19049427 | Rare:37 | ||||
chr9:19102844-19103049 | Common:2; Rare:85 | ||||
chr9:19380190-19380339 | Common:4; Rare:74 | ||||
chr9:20622394-20622668 | Rare:102 | ||||
chr9:20684063-20684289 | Common:3; Rare:91 | ||||
chr9:21802457-21802687 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
chr9:26892738-26892865 | Rare:66 | ||||
chr9:26947024-26947281 | Common:1; Rare:100 | ||||
chr9:26947366-26947566 | Common:1; Rare:67 |