| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25057513-25057717 | Common:3; Rare:44 | ||||
| chr20:25057911-25057933 | Common:1; Rare:4 | ||||
| chr20:25058076-25058196 | Common:1; Rare:26 | ||||
| chr20:25058307-25058497 | Common:4; Rare:44 | ||||
| chr20:25058594-25058687 | Common:1; Rare:12 | ||||
| chr20:25195425-25195806 | Common:4; Rare:108 | ||||
| chr20:25247898-25248382 | Common:2; Rare:189 | ||||
| chr20:25389713-25389795 | Rare:22 | ||||
| chr20:25390389-25390615 | Common:10; Rare:100 | ||||
| chr20:25390723-25391170 | Common:5; Rare:166; Clinvar:4; Clinvar (benign):3 | ||||
| chr20:25407465-25407798 | Common:4; Rare:116; Clinvar (pathogenic):1 | ||||
| chr20:25623639-25624243 | Common:2; Rare:217 | ||||
| chr20:25624378-25624520 | Common:1; Rare:44 | ||||
| chr20:25696483-25697080 | Common:4; Rare:191 | ||||
| chr20:31514332-31514567 | Common:6; Rare:100 |