| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31719375-31719651 | Common:2; Rare:42 | ||||
| chr20:32369745-32369997 | Rare:58 | ||||
| chr20:32850294-32850529 | Rare:34 | ||||
| chr20:32853274-32853493 | Rare:29 | ||||
| chr20:32854451-32854668 | Rare:36 | ||||
| chr20:32854682-32854931 | Common:4; Rare:80 | ||||
| chr20:32855795-32856083 | Rare:53 | ||||
| chr20:33350801-33351078 | Rare:33 | ||||
| chr20:33812319-33812416 | Rare:10 | ||||
| chr20:33813167-33813300 | Rare:15 | ||||
| chr20:34048878-34049165 | Rare:53 | ||||
| chr20:34246239-34246525 | Common:4; Rare:28 | ||||
| chr20:34257113-34257274 | Common:2; Rare:25 | ||||
| chr20:34292434-34292630 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr20:34434321-34434588 | Rare:42 |