| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5119779-5120202 | Common:1; Rare:143 | ||||
| chr20:5610913-5611225 | Common:3; Rare:114 | ||||
| chr20:5950372-5950720 | Common:8; Rare:109 | ||||
| chr20:5950894-5950946 | Common:2; Rare:12 | ||||
| chr20:6005804-6005945 | Rare:34 | ||||
| chr20:6122953-6123033 | Rare:24; Clinvar:1 | ||||
| chr20:8114346-8114558 | Common:9; Rare:78 | ||||
| chr20:8114911-8114943 | Rare:6 | ||||
| chr20:10034838-10035104 | Common:5; Rare:104 | ||||
| chr20:10433968-10434012 | Common:1; Rare:9 | ||||
| chr20:10434503-10434696 | Common:1; Rare:61 | ||||
| chr20:11890535-11890897 | Common:4; Rare:116 | ||||
| chr20:11892375-11892516 | Common:1; Rare:28 | ||||
| chr20:13638898-13639048 | Common:1; Rare:43 | ||||
| chr20:13784860-13785112 | Common:2; Rare:119; Clinvar:1; Clinvar (benign):3 |