| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31547305-31547438 | Rare:34 | ||||
| chr20:31722780-31722886 | Rare:24 | ||||
| chr20:31722893-31722963 | Rare:20 | ||||
| chr20:31739098-31739362 | Common:1; Rare:67 | ||||
| chr20:31845597-31845813 | Rare:48 | ||||
| chr20:32207694-32207939 | Common:3; Rare:94 | ||||
| chr20:32819719-32820006 | Common:3; Rare:99 | ||||
| chr20:33401473-33401589 | Rare:34 | ||||
| chr20:33720203-33720528 | Common:4; Rare:87 | ||||
| chr20:33993771-33994120 | Common:1; Rare:125 | ||||
| chr20:34112104-34112426 | Rare:105 | ||||
| chr20:34303296-34303481 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:34516278-34516451 | Common:3; Rare:69 | ||||
| chr20:34558520-34558846 | Common:1; Rare:99 | ||||
| chr20:34677078-34677304 | Rare:58 |