| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:681112-681235 | Rare:47 | ||||
| chr4:705587-705928 | Common:1; Rare:114 | ||||
| chr4:932135-932492 | Common:2; Rare:137 | ||||
| chr4:986894-987197 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):3 | ||||
| chr4:1113524-1113630 | Common:2; Rare:38 | ||||
| chr4:1289650-1289925 | Common:1; Rare:93 | ||||
| chr4:1712618-1712865 | Common:1; Rare:74 | ||||
| chr4:1720546-1720638 | Rare:28 | ||||
| chr4:1721326-1721524 | Common:2; Rare:56 | ||||
| chr4:1723408-1723759 | Common:1; Rare:131 | ||||
| chr4:1856097-1856404 | Rare:80 | ||||
| chr4:2041912-2042017 | Common:1; Rare:41 | ||||
| chr4:2255433-2255738 | Common:1; Rare:61 | ||||
| chr4:2468878-2469200 | Common:5; Rare:133 | ||||
| chr4:2798470-2798606 | Common:4; Rare:23 |