| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:21303689-21303846 | Rare:51 | ||||
| chr20:25623933-25624179 | Common:1; Rare:97 | ||||
| chr20:32207712-32207921 | Common:2; Rare:78 | ||||
| chr20:35284505-35284813 | Common:3; Rare:89 | ||||
| chr20:35699185-35699255 | Rare:9 | ||||
| chr20:35699336-35699450 | Rare:33 | ||||
| chr20:36236436-36236523 | Rare:19 | ||||
| chr20:38033431-38033767 | Common:2; Rare:99 | ||||
| chr20:44210620-44211130 | Common:5; Rare:179 | ||||
| chr20:44651617-44651795 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr20:44715271-44715412 | Common:8; Rare:50 | ||||
| chr20:45406518-45406731 | Rare:59 | ||||
| chr20:45791913-45792002 | Common:1; Rare:35 | ||||
| chr20:45857326-45857618 | Common:3; Rare:78 | ||||
| chr20:45891227-45891435 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 |