| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49046183-49046370 | Common:3; Rare:57 | ||||
| chr20:49278029-49278272 | Rare:66 | ||||
| chr20:49568047-49568159 | Common:6; Rare:31 | ||||
| chr20:49915496-49915818 | Common:4; Rare:88 | ||||
| chr20:50691303-50691367 | Rare:14 | ||||
| chr20:50958497-50958853 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:53593793-53593882 | Common:1; Rare:30 | ||||
| chr20:56392191-56392379 | Rare:46 | ||||
| chr20:56392575-56392683 | Common:1; Rare:26 | ||||
| chr20:57329683-57329858 | Common:1; Rare:75 | ||||
| chr20:58309417-58309715 | Common:2; Rare:118 | ||||
| chr20:58651133-58651311 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58651662-58651847 | Rare:35 | ||||
| chr20:59007023-59007070 | Rare:17 | ||||
| chr20:59042757-59042987 | Common:1; Rare:81 |