| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145482869-145483001 | Rare:21 | ||||
| chr4:145619302-145619396 | Rare:44 | ||||
| chr4:147617254-147617455 | Common:1; Rare:44 | ||||
| chr4:147684127-147684300 | Rare:74 | ||||
| chr4:147731891-147732088 | Common:1; Rare:64 | ||||
| chr4:148442375-148442712 | Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:150581714-150581930 | Rare:43 | ||||
| chr4:151015709-151015849 | Rare:68 | ||||
| chr4:151099491-151099713 | Common:3; Rare:89 | ||||
| chr4:151100187-151100580 | Common:1; Rare:80 | ||||
| chr4:151408894-151409193 | Common:4; Rare:96 | ||||
| chr4:152536053-152536407 | Common:2; Rare:136 | ||||
| chr4:152779724-152780165 | Common:2; Rare:114 | ||||
| chr4:153344508-153344714 | Common:4; Rare:54 | ||||
| chr4:153789017-153789128 | Rare:39 |