| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147684118-147684293 | Common:1; Rare:69 | ||||
| chr4:151015210-151015364 | Rare:42 | ||||
| chr4:151015722-151015835 | Rare:50 | ||||
| chr4:151099259-151099713 | Common:3; Rare:131 | ||||
| chr4:151408894-151409267 | Common:4; Rare:117 | ||||
| chr4:152352549-152352887 | Rare:99; Clinvar:1 | ||||
| chr4:152679874-152680122 | Rare:84 | ||||
| chr4:152779711-152780009 | Common:1; Rare:81 | ||||
| chr4:152936146-152936360 | Common:3; Rare:54 | ||||
| chr4:153204367-153204431 | Rare:11 | ||||
| chr4:154550366-154550504 | Rare:45 | ||||
| chr4:156971074-156971183 | Rare:17 | ||||
| chr4:158210321-158210584 | Common:3; Rare:64 | ||||
| chr4:158671830-158672139 | Common:4; Rare:82 | ||||
| chr4:158672208-158672313 | Common:1; Rare:21; Clinvar:1; Clinvar (benign):1 |