| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2840405-2840782 | Common:3; Rare:127 | ||||
| chr20:3173521-3173677 | Common:1; Rare:57 | ||||
| chr20:3209126-3209356 | Common:1; Rare:46 | ||||
| chr20:3209429-3209544 | Common:1; Rare:39 | ||||
| chr20:3239126-3239365 | Common:1; Rare:79 | ||||
| chr20:3239552-3239719 | Common:1; Rare:50 | ||||
| chr20:3407565-3407711 | Common:2; Rare:41 | ||||
| chr20:3407903-3408049 | Rare:38 | ||||
| chr20:3470945-3471081 | Common:1; Rare:60 | ||||
| chr20:3767716-3768056 | Common:4; Rare:108 | ||||
| chr20:3795656-3795839 | Common:2; Rare:48 | ||||
| chr20:3820466-3820582 | Rare:47 | ||||
| chr20:3846724-3846894 | Rare:50 | ||||
| chr20:3888899-3888929 | Rare:7 | ||||
| chr20:3889157-3889415 | Common:1; Rare:135; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 |