| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:56468458-56468749 | Rare:174 | ||||
| chr20:56629062-56629356 | Common:1; Rare:171 | ||||
| chr20:57351142-57351422 | Common:4; Rare:124 | ||||
| chr20:57391218-57391449 | Common:14; Rare:180 | ||||
| chr20:57709860-57710250 | Common:1; Rare:164 | ||||
| chr20:58309417-58309750 | Common:4; Rare:256 | ||||
| chr20:58388989-58389341 | Common:7; Rare:308; Clinvar:9; Clinvar (benign):3 | ||||
| chr20:58651025-58651349 | Common:5; Rare:164; Clinvar:4; Clinvar (benign):2 | ||||
| chr20:58652280-58652730 | Common:6; Rare:255 | ||||
| chr20:58692683-58692940 | Common:5; Rare:138 | ||||
| chr20:58888788-58889202 | Common:2; Rare:252 | ||||
| chr20:58890800-58891105 | Common:5; Rare:198 | ||||
| chr20:58891188-58891624 | Common:8; Rare:263; Clinvar:2 | ||||
| chr20:58891721-58892190 | Common:7; Rare:313; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr20:58892137-58892310 | Common:5; Rare:62 |