| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43670350-43670650 | Common:3; Rare:56 | ||||
| chr20:43812162-43812947 | Common:6; Rare:235 | ||||
| chr20:44089960-44090280 | Common:2; Rare:64 | ||||
| chr20:44137136-44137546 | Common:6; Rare:239 | ||||
| chr20:44208831-44209336 | Common:2; Rare:136 | ||||
| chr20:44287260-44287580 | Common:3; Rare:52 | ||||
| chr20:44302289-44302627 | Common:3; Rare:140 | ||||
| chr20:44319936-44320230 | Common:4; Rare:89 | ||||
| chr20:44370510-44370980 | Common:2; Rare:70 | ||||
| chr20:44407438-44407707 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr20:44553091-44553977 | Common:5; Rare:204 | ||||
| chr20:44616694-44616855 | Common:2; Rare:30 | ||||
| chr20:44642944-44643068 | Rare:20 | ||||
| chr20:44678280-44678620 | Common:3; Rare:39 | ||||
| chr20:44728841-44729199 | Common:5; Rare:88 |