| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:664185-664270 | Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:673797-673960 | Common:1; Rare:59 | ||||
| chr4:674210-674618 | Common:4; Rare:186 | ||||
| chr4:681142-681235 | Rare:33 | ||||
| chr4:932250-932492 | Common:2; Rare:95 | ||||
| chr4:1113510-1113630 | Common:2; Rare:43 | ||||
| chr4:1289659-1289925 | Common:1; Rare:88 | ||||
| chr4:1346950-1347229 | Common:4; Rare:83 | ||||
| chr4:1720518-1720608 | Rare:20 | ||||
| chr4:1721324-1721549 | Common:4; Rare:65 | ||||
| chr4:2008958-2009008 | Rare:26 | ||||
| chr4:2041891-2042052 | Common:1; Rare:60 | ||||
| chr4:2468862-2469187 | Common:4; Rare:124 | ||||
| chr4:2843678-2844011 | Common:3; Rare:123 | ||||
| chr4:2934767-2934931 | Common:4; Rare:74 |