| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31605132-31605295 | Common:5; Rare:65 | ||||
| chr20:31722845-31722979 | Rare:31 | ||||
| chr20:32109694-32109746 | Rare:24 | ||||
| chr20:32207683-32207921 | Common:2; Rare:87 | ||||
| chr20:32358132-32358364 | Common:2; Rare:59 | ||||
| chr20:33401499-33401601 | Rare:26 | ||||
| chr20:33731864-33732050 | Rare:60 | ||||
| chr20:33993079-33993291 | Rare:57 | ||||
| chr20:33993766-33993951 | Common:1; Rare:64 | ||||
| chr20:34112212-34112471 | Rare:82 | ||||
| chr20:34302961-34303299 | Rare:108; Clinvar (benign):1 | ||||
| chr20:34558502-34558756 | Common:1; Rare:66 | ||||
| chr20:34677090-34677379 | Rare:72 | ||||
| chr20:34704132-34704348 | Common:1; Rare:69 | ||||
| chr20:34955741-34956087 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):2 |