| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5950278-5950729 | Common:8; Rare:138 | ||||
| chr20:5950870-5950997 | Common:2; Rare:30 | ||||
| chr20:6005808-6006148 | Common:2; Rare:95 | ||||
| chr20:6006303-6006548 | Common:2; Rare:64 | ||||
| chr20:6122788-6123154 | Common:4; Rare:87; Clinvar:7; Clinvar (benign):4 | ||||
| chr20:10218809-10219007 | Rare:48 | ||||
| chr20:10219472-10219793 | Common:1; Rare:60 | ||||
| chr20:10434415-10434676 | Common:1; Rare:76 | ||||
| chr20:10435034-10435372 | Rare:88 | ||||
| chr20:10641264-10641671 | Common:3; Rare:111; Clinvar:7; Clinvar (benign):6 | ||||
| chr20:10641675-10641796 | Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:10673666-10673727 | Rare:9 | ||||
| chr20:10673733-10673934 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:10673936-10674138 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:13784869-13785094 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):3 |