| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44582443-44582646 | Rare:30 | ||||
| chr20:44614291-44614670 | Common:1; Rare:78 | ||||
| chr20:44651687-44651845 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr20:44714610-44714960 | Rare:78 | ||||
| chr20:44885602-44885885 | Common:4; Rare:93 | ||||
| chr20:44960370-44960521 | Common:1; Rare:55 | ||||
| chr20:44966376-44966577 | Common:1; Rare:78 | ||||
| chr20:45348365-45348584 | Common:1; Rare:69 | ||||
| chr20:45362994-45363226 | Rare:68 | ||||
| chr20:45363324-45363527 | Common:1; Rare:47 | ||||
| chr20:45406541-45406760 | Rare:57 | ||||
| chr20:45415963-45416159 | Rare:52 | ||||
| chr20:45469494-45469759 | Common:1; Rare:65 | ||||
| chr20:45791879-45792005 | Common:1; Rare:49 | ||||
| chr20:45833255-45833629 | Common:1; Rare:61 |