| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32109691-32109749 | Rare:29 | ||||
| chr20:32207686-32207944 | Common:3; Rare:100 | ||||
| chr20:32483366-32483815 | Common:1; Rare:69 | ||||
| chr20:33401491-33401584 | Rare:24 | ||||
| chr20:33993133-33993411 | Rare:60 | ||||
| chr20:34112189-34112412 | Rare:64 | ||||
| chr20:34363171-34363337 | Rare:43 | ||||
| chr20:34516278-34516443 | Common:3; Rare:60 | ||||
| chr20:34558533-34558727 | Common:1; Rare:48 | ||||
| chr20:34677086-34677318 | Rare:59 | ||||
| chr20:34872820-34872931 | Rare:40 | ||||
| chr20:34955741-34955823 | Common:1; Rare:30; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35147306-35147416 | Rare:32 | ||||
| chr20:35284552-35284870 | Common:2; Rare:85 | ||||
| chr20:35664880-35665015 | Common:1; Rare:34 |