| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31722726-31722940 | Rare:56 | ||||
| chr20:31723511-31723715 | Common:1; Rare:58 | ||||
| chr20:31739102-31739363 | Common:1; Rare:67 | ||||
| chr20:32207674-32207986 | Common:3; Rare:118 | ||||
| chr20:32358477-32358735 | Common:2; Rare:80; Clinvar:10; Clinvar (benign):2 | ||||
| chr20:33401482-33401634 | Rare:41 | ||||
| chr20:33811172-33811684 | Common:2; Rare:145 | ||||
| chr20:33993029-33993291 | Common:1; Rare:70 | ||||
| chr20:33993723-33993978 | Common:2; Rare:87 | ||||
| chr20:33993985-33994130 | Rare:47 | ||||
| chr20:34112102-34112423 | Rare:104 | ||||
| chr20:34302973-34303319 | Common:1; Rare:125; Clinvar (benign):2 | ||||
| chr20:34516275-34516460 | Common:3; Rare:78 | ||||
| chr20:34558518-34558766 | Common:1; Rare:70 | ||||
| chr20:34677072-34677320 | Rare:64 |