| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:21303600-21304200 | Rare:251 | ||||
| chr20:23350525-23350889 | Common:3; Rare:198 | ||||
| chr20:23361800-23362221 | Common:8; Rare:246 | ||||
| chr20:23421411-23421657 | Common:6; Rare:186 | ||||
| chr20:24992644-24992917 | Common:14; Rare:223 | ||||
| chr20:25195598-25195899 | Common:7; Rare:156 | ||||
| chr20:25247931-25248121 | Common:2; Rare:140 | ||||
| chr20:25390713-25391002 | Common:10; Rare:227; Clinvar:8; Clinvar (benign):6 | ||||
| chr20:25407543-25407776 | Common:3; Rare:151; Clinvar (pathogenic):1 | ||||
| chr20:25623921-25624211 | Common:2; Rare:189 | ||||
| chr20:25624340-25624740 | Common:5; Rare:142 | ||||
| chr20:25696657-25697109 | Common:6; Rare:207 | ||||
| chr20:31514390-31514653 | Common:1; Rare:91 | ||||
| chr20:31547257-31547479 | Rare:106 | ||||
| chr20:31605072-31605302 | Common:12; Rare:177 |