| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:142474395-142474710 | Rare:53 | ||||
| chr4:142846453-142846635 | Common:1; Rare:37 | ||||
| chr4:145098148-145098348 | Rare:70 | ||||
| chr4:145180569-145180872 | Common:1; Rare:81 | ||||
| chr4:151760983-151761258 | Common:2; Rare:84 | ||||
| chr4:152779762-152780013 | Common:1; Rare:68 | ||||
| chr4:158671853-158672313 | Common:5; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723335-158723484 | Common:2; Rare:67 | ||||
| chr4:165327385-165327692 | Common:3; Rare:90 | ||||
| chr4:169010266-169010503 | Common:1; Rare:75 | ||||
| chr4:169270941-169271168 | Common:1; Rare:75 | ||||
| chr4:173370690-173370962 | Common:2; Rare:68 | ||||
| chr4:174522487-174522613 | Rare:41; Clinvar:2 | ||||
| chr4:176319754-176320042 | Common:3; Rare:105 | ||||
| chr4:177442371-177442530 | Rare:96; Clinvar:2; Clinvar (pathogenic):1 |