| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31722536-31722684 | Rare:32 | ||||
| chr20:31723519-31723721 | Common:1; Rare:56 | ||||
| chr20:31739136-31739504 | Common:1; Rare:87 | ||||
| chr20:32109421-32109755 | Common:2; Rare:89 | ||||
| chr20:32207676-32207944 | Common:3; Rare:102 | ||||
| chr20:33401476-33401633 | Rare:44 | ||||
| chr20:33720271-33720510 | Common:4; Rare:54 | ||||
| chr20:33731885-33732010 | Rare:44 | ||||
| chr20:34112123-34112448 | Rare:113 | ||||
| chr20:34302951-34303173 | Rare:65 | ||||
| chr20:34303318-34303492 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:34516336-34516451 | Rare:49 | ||||
| chr20:34677090-34677331 | Rare:60 | ||||
| chr20:34872827-34873008 | Common:1; Rare:56 | ||||
| chr20:34955741-34955874 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):2 |