| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31723502-31723759 | Common:1; Rare:81 | ||||
| chr20:31739093-31739357 | Common:2; Rare:68 | ||||
| chr20:32207706-32208012 | Common:3; Rare:118 | ||||
| chr20:32483444-32483803 | Common:1; Rare:56 | ||||
| chr20:32819740-32819987 | Common:3; Rare:90 | ||||
| chr20:33401465-33401609 | Rare:37 | ||||
| chr20:33994009-33994120 | Rare:34 | ||||
| chr20:34112101-34112406 | Rare:98 | ||||
| chr20:34302966-34303295 | Rare:104; Clinvar (benign):1 | ||||
| chr20:34677078-34677325 | Rare:64 | ||||
| chr20:34955733-34955929 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:35092765-35092948 | Common:2; Rare:86 | ||||
| chr20:35147221-35147461 | Common:1; Rare:86 | ||||
| chr20:35171814-35172119 | Common:1; Rare:57 | ||||
| chr20:35174911-35175037 | Common:1; Rare:55 |