| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31723513-31723715 | Common:1; Rare:57 | ||||
| chr20:31723904-31724079 | Rare:34 | ||||
| chr20:31739093-31739369 | Common:2; Rare:73 | ||||
| chr20:31845569-31845749 | Rare:40 | ||||
| chr20:31967474-31967549 | Rare:12 | ||||
| chr20:32207651-32207939 | Common:3; Rare:103 | ||||
| chr20:32483440-32483721 | Common:1; Rare:47 | ||||
| chr20:32819719-32819987 | Common:3; Rare:94 | ||||
| chr20:33401481-33401618 | Rare:34 | ||||
| chr20:33562077-33562450 | Rare:64 | ||||
| chr20:33720210-33720540 | Common:4; Rare:83 | ||||
| chr20:33993721-33993993 | Common:3; Rare:96 | ||||
| chr20:34112185-34112427 | Rare:72 | ||||
| chr20:34303281-34303399 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:34516278-34516451 | Common:3; Rare:69 |