| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44736404-44737029 | Common:7; Rare:142 | ||||
| chr20:44747149-44747549 | Common:2; Rare:80 | ||||
| chr20:44765722-44766219 | Common:4; Rare:226 | ||||
| chr20:44911520-44911850 | Common:2; Rare:104 | ||||
| chr20:44955616-44956099 | Rare:218 | ||||
| chr20:45336755-45336904 | Common:2; Rare:31; Clinvar (benign):1 | ||||
| chr20:45341815-45342310 | Common:2; Rare:129 | ||||
| chr20:45342329-45342563 | Rare:60 | ||||
| chr20:45342802-45343144 | Common:2; Rare:111 | ||||
| chr20:45343393-45343769 | Common:2; Rare:189 | ||||
| chr20:45344231-45344864 | Common:6; Rare:203 | ||||
| chr20:45345499-45345871 | Common:2; Rare:79 | ||||
| chr20:45346049-45347003 | Common:11; Rare:295 | ||||
| chr20:45419298-45419763 | Common:5; Rare:245; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr20:45436870-45436995 | Common:1; Rare:31 |