| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145180467-145180853 | Common:1; Rare:113 | ||||
| chr4:145481645-145481736 | Rare:22 | ||||
| chr4:145619296-145619416 | Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:145938786-145938969 | Rare:49 | ||||
| chr4:146522327-146522468 | Common:3; Rare:55 | ||||
| chr4:147617217-147617473 | Common:1; Rare:60 | ||||
| chr4:147684096-147684309 | Common:1; Rare:91 | ||||
| chr4:150078708-150078836 | Common:1; Rare:33 | ||||
| chr4:151015216-151015407 | Rare:51 | ||||
| chr4:151015684-151015821 | Rare:56 | ||||
| chr4:151099313-151099850 | Common:3; Rare:161 | ||||
| chr4:151760929-151761215 | Rare:114 | ||||
| chr4:152352639-152352785 | Rare:47 | ||||
| chr4:152536079-152536438 | Common:3; Rare:132 | ||||
| chr4:152679935-152680156 | Rare:52 |