| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10511675-10511798 | Rare:21 | ||||
| chr20:10540651-10540960 | Rare:46 | ||||
| chr20:10555949-10556276 | Rare:54 | ||||
| chr20:10643118-10643132 | Rare:7 | ||||
| chr20:10643771-10644065 | Common:1; Rare:65; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:10659788-10659865 | Common:1; Rare:16 | ||||
| chr20:10667795-10668086 | Common:1; Rare:62 | ||||
| chr20:10669343-10669540 | Rare:39 | ||||
| chr20:10670740-10670946 | Rare:43 | ||||
| chr20:10671095-10671160 | Rare:8 | ||||
| chr20:10671592-10671696 | Rare:18 | ||||
| chr20:10672363-10672695 | Common:2; Rare:78 | ||||
| chr20:11158242-11158563 | Common:2; Rare:76 | ||||
| chr20:11455563-11455608 | Rare:10 | ||||
| chr20:11455612-11455651 | Common:1; Rare:4 |