| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32207643-32207951 | Common:3; Rare:112 | ||||
| chr20:32483440-32483721 | Common:1; Rare:47 | ||||
| chr20:33401473-33401634 | Rare:46 | ||||
| chr20:33720215-33720588 | Common:4; Rare:87 | ||||
| chr20:33811172-33811499 | Common:1; Rare:102 | ||||
| chr20:33993939-33994131 | Rare:72 | ||||
| chr20:33994426-33994578 | Rare:32 | ||||
| chr20:34112100-34112556 | Common:1; Rare:144 | ||||
| chr20:34303274-34303337 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:34303345-34303492 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:34363247-34363330 | Rare:26 | ||||
| chr20:34516273-34516455 | Common:3; Rare:76 | ||||
| chr20:34558533-34558776 | Common:1; Rare:63 | ||||
| chr20:34677081-34677318 | Rare:62 | ||||
| chr20:34872792-34872973 | Rare:64 |