| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43590597-43590990 | Common:1; Rare:87 | ||||
| chr20:44187017-44187307 | Common:4; Rare:68 | ||||
| chr20:44187485-44187745 | Common:1; Rare:45 | ||||
| chr20:44210697-44211124 | Common:5; Rare:153 | ||||
| chr20:44355578-44355746 | Common:1; Rare:25; Clinvar:1 | ||||
| chr20:44521916-44522213 | Common:2; Rare:96 | ||||
| chr20:44531800-44531978 | Common:1; Rare:56 | ||||
| chr20:44582063-44582373 | Common:1; Rare:57 | ||||
| chr20:44582427-44582660 | Rare:34 | ||||
| chr20:44614256-44614583 | Common:1; Rare:56 | ||||
| chr20:44651662-44651827 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr20:44714616-44714908 | Rare:62 | ||||
| chr20:44885602-44885885 | Common:4; Rare:93 | ||||
| chr20:44909866-44910137 | Common:2; Rare:109 | ||||
| chr20:44966274-44966577 | Common:2; Rare:112 |