| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32483453-32483684 | Rare:45 | ||||
| chr20:32743401-32743604 | Common:1; Rare:49 | ||||
| chr20:32819714-32820006 | Common:3; Rare:101 | ||||
| chr20:33401481-33401634 | Rare:41 | ||||
| chr20:33993078-33993271 | Rare:52 | ||||
| chr20:34112102-34112427 | Rare:107 | ||||
| chr20:34303275-34303393 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:34516278-34516451 | Common:3; Rare:69 | ||||
| chr20:34677086-34677122 | Rare:14 | ||||
| chr20:34872821-34872928 | Rare:39 | ||||
| chr20:34955703-34955868 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35147265-35147383 | Common:1; Rare:45 | ||||
| chr20:35171765-35172114 | Common:2; Rare:69 | ||||
| chr20:35284728-35284921 | Common:2; Rare:59 | ||||
| chr20:35411958-35412083 | Rare:46 |