| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34363137-34363377 | Rare:66 | ||||
| chr20:34515756-34515934 | Rare:33 | ||||
| chr20:34516303-34516448 | Common:3; Rare:55 | ||||
| chr20:34516597-34516759 | Rare:62 | ||||
| chr20:34676641-34676911 | Common:1; Rare:66 | ||||
| chr20:34677034-34677423 | Rare:100 | ||||
| chr20:34677531-34677578 | Rare:12 | ||||
| chr20:34704128-34704362 | Common:1; Rare:74 | ||||
| chr20:34704580-34704760 | Common:2; Rare:37 | ||||
| chr20:34825169-34825371 | Rare:50 | ||||
| chr20:34825549-34825845 | Rare:120 | ||||
| chr20:34872767-34872952 | Rare:66 | ||||
| chr20:34876257-34876599 | Common:3; Rare:93 | ||||
| chr20:34955293-34955579 | Common:2; Rare:59 | ||||
| chr20:34955629-34955971 | Common:1; Rare:109; Clinvar:3; Clinvar (benign):3 |