| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31739098-31739363 | Common:1; Rare:69 | ||||
| chr20:31819100-31819400 | Common:2; Rare:67 | ||||
| chr20:31845582-31845749 | Rare:39 | ||||
| chr20:31870134-31870241 | Rare:17 | ||||
| chr20:32207694-32207950 | Common:3; Rare:102 | ||||
| chr20:33401481-33401643 | Rare:44 | ||||
| chr20:33993078-33993291 | Rare:57 | ||||
| chr20:34112102-34112419 | Rare:104 | ||||
| chr20:34303254-34303537 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:34516273-34516451 | Common:3; Rare:73 | ||||
| chr20:34558533-34558640 | Rare:26 | ||||
| chr20:34677083-34677329 | Rare:63 | ||||
| chr20:34872821-34872982 | Rare:56 | ||||
| chr20:34955733-34955929 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:35147293-35147437 | Rare:47 |