| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:168146009-168146098 | Common:1; Rare:22 | ||||
| chr4:168150695-168151002 | Common:3; Rare:52 | ||||
| chr4:168169365-168169624 | Common:1; Rare:37 | ||||
| chr4:168174404-168174733 | Common:1; Rare:63 | ||||
| chr4:168421815-168421975 | Common:1; Rare:51 | ||||
| chr4:168833350-168833511 | Common:2; Rare:28 | ||||
| chr4:168836040-168836268 | Common:1; Rare:39 | ||||
| chr4:168836693-168837015 | Common:2; Rare:55 | ||||
| chr4:168859329-168859375 | Rare:4 | ||||
| chr4:168863066-168863157 | Common:2; Rare:7 | ||||
| chr4:168869232-168869393 | Rare:26 | ||||
| chr4:168869660-168869935 | Common:1; Rare:37 | ||||
| chr4:168890813-168891057 | Rare:63; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:168903504-168903915 | Rare:87; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:168904770-168904997 | Common:3; Rare:39 |