| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31722854-31722963 | Rare:28 | ||||
| chr20:31723485-31723775 | Common:2; Rare:97 | ||||
| chr20:31739014-31739404 | Common:4; Rare:100 | ||||
| chr20:31845560-31845800 | Rare:51 | ||||
| chr20:31870429-31870638 | Common:1; Rare:63 | ||||
| chr20:31879550-31880000 | Rare:123 | ||||
| chr20:31880058-31880190 | Rare:44 | ||||
| chr20:31967892-31968176 | Common:2; Rare:68 | ||||
| chr20:32109379-32109584 | Common:1; Rare:43 | ||||
| chr20:32109913-32110313 | Rare:137 | ||||
| chr20:32207719-32207981 | Common:3; Rare:103 | ||||
| chr20:32277561-32277669 | Rare:26 | ||||
| chr20:32357897-32358123 | Common:2; Rare:69 | ||||
| chr20:32358529-32358779 | Common:1; Rare:75; Clinvar:9; Clinvar (benign):1 | ||||
| chr20:32483420-32483870 | Common:1; Rare:68 |