| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44521379-44522280 | Common:12; Rare:498 | ||||
| chr20:44531707-44531992 | Common:3; Rare:191 | ||||
| chr20:44651663-44651891 | Common:3; Rare:138; Clinvar (benign):3 | ||||
| chr20:44714538-44714948 | Rare:184 | ||||
| chr20:44745350-44745650 | Common:26; Rare:80 | ||||
| chr20:44745670-44746040 | Rare:251 | ||||
| chr20:44746162-44746316 | Common:1; Rare:38 | ||||
| chr20:44810441-44810706 | Common:9; Rare:267 | ||||
| chr20:44884983-44885861 | Common:21; Rare:479 | ||||
| chr20:44885840-44886370 | Rare:182 | ||||
| chr20:44909852-44910372 | Common:5; Rare:325 | ||||
| chr20:44960297-44960601 | Common:3; Rare:256 | ||||
| chr20:44966246-44966611 | Common:5; Rare:343 | ||||
| chr20:45254539-45254673 | Rare:25 | ||||
| chr20:45348304-45348683 | Common:6; Rare:263 |