| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:57620410-57620556 | Common:1; Rare:30 | ||||
| chr20:58651532-58651850 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):4 | ||||
| chr20:58891201-58891371 | Common:3; Rare:59 | ||||
| chr20:58894695-58894766 | Rare:16 | ||||
| chr20:58894776-58895099 | Common:2; Rare:64 | ||||
| chr20:58903550-58903759 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:58909135-58909802 | Common:3; Rare:163; Clinvar:2; Clinvar (pathogenic):6 | ||||
| chr20:58910056-58910402 | Rare:91 | ||||
| chr20:58988662-58988977 | Common:2; Rare:73 | ||||
| chr20:59006987-59006998 | |||||
| chr20:59940295-59940485 | Rare:78 | ||||
| chr20:62143288-62143808 | Common:7; Rare:220 | ||||
| chr20:62302691-62303031 | Common:2; Rare:94 | ||||
| chr20:62804583-62804866 | Common:2; Rare:79 | ||||
| chr20:62926455-62926640 | Common:2; Rare:58 |