Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:31722783-31722956 | Rare:42 | ||||
chr20:31739102-31739357 | Common:1; Rare:64 | ||||
chr20:32207724-32207944 | Common:3; Rare:87 | ||||
chr20:33401481-33401634 | Rare:41 | ||||
chr20:33993073-33993258 | Rare:52 | ||||
chr20:33994011-33994122 | Rare:34 | ||||
chr20:34112096-34112430 | Rare:109 | ||||
chr20:34516279-34516451 | Common:3; Rare:69 | ||||
chr20:34677086-34677291 | Rare:54 | ||||
chr20:34872821-34872928 | Rare:39 | ||||
chr20:34955725-34955823 | Common:1; Rare:36; Clinvar:3; Clinvar (benign):3 | ||||
chr20:35092759-35092912 | Common:2; Rare:81 | ||||
chr20:35278034-35278211 | Common:3; Rare:63 | ||||
chr20:35631540-35631731 | Common:3; Rare:65 | ||||
chr20:35664867-35665032 | Common:1; Rare:44 |