| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3767716-3768076 | Common:5; Rare:113 | ||||
| chr20:3846724-3846908 | Common:1; Rare:52 | ||||
| chr20:3889161-3889387 | Common:1; Rare:115; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4686301-4686714 | Common:2; Rare:107; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:5112959-5113194 | Rare:100 | ||||
| chr20:5119849-5120196 | Common:1; Rare:120 | ||||
| chr20:5610865-5611144 | Common:2; Rare:94 | ||||
| chr20:5750314-5750466 | Rare:35 | ||||
| chr20:5950324-5950720 | Common:8; Rare:122 | ||||
| chr20:6005795-6005947 | Rare:37 | ||||
| chr20:6053864-6054204 | Common:4; Rare:49 | ||||
| chr20:6054419-6054780 | Common:2; Rare:67 | ||||
| chr20:6122916-6123053 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:8601125-8601379 | Common:1; Rare:55 | ||||
| chr20:9068508-9068887 | Common:2; Rare:93 |