| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31605119-31605477 | Common:9; Rare:193 | ||||
| chr20:31722839-31722938 | Rare:27 | ||||
| chr20:31739075-31739364 | Common:2; Rare:75 | ||||
| chr20:31845540-31845729 | Common:1; Rare:39 | ||||
| chr20:32207712-32207944 | Common:3; Rare:91 | ||||
| chr20:33401481-33401618 | Rare:34 | ||||
| chr20:33811535-33811610 | Rare:12 | ||||
| chr20:34516256-34516459 | Common:3; Rare:82 | ||||
| chr20:34677063-34677291 | Rare:66 | ||||
| chr20:34955743-34955929 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35278046-35278321 | Common:7; Rare:96 | ||||
| chr20:35284552-35284892 | Common:2; Rare:90 | ||||
| chr20:35556969-35557249 | Common:2; Rare:87 | ||||
| chr20:35699185-35699456 | Rare:73; Clinvar (benign):3 | ||||
| chr20:35742097-35742601 | Common:5; Rare:154 |