| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44247113-44247317 | Rare:54 | ||||
| chr20:44311139-44311349 | Common:1; Rare:74 | ||||
| chr20:44475761-44475931 | Rare:79 | ||||
| chr20:44522033-44522243 | Common:2; Rare:62 | ||||
| chr20:44531721-44531937 | Common:1; Rare:72 | ||||
| chr20:44651657-44651848 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr20:44652224-44652374 | Rare:22 | ||||
| chr20:44885363-44885736 | Common:5; Rare:109 | ||||
| chr20:44909927-44910069 | Common:1; Rare:49 | ||||
| chr20:44960325-44960572 | Common:1; Rare:94 | ||||
| chr20:44966294-44966580 | Common:2; Rare:110 | ||||
| chr20:45362895-45363307 | Common:1; Rare:122 | ||||
| chr20:45363366-45363608 | Common:2; Rare:66 | ||||
| chr20:45406400-45406720 | Rare:85 | ||||
| chr20:45407310-45407650 | Rare:67 |