| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145619322-145619394 | Rare:28 | ||||
| chr4:147684102-147684286 | Common:1; Rare:71 | ||||
| chr4:151099511-151099627 | Common:2; Rare:45 | ||||
| chr4:152779584-152780183 | Common:3; Rare:145 | ||||
| chr4:158172610-158172736 | Rare:25 | ||||
| chr4:158671825-158672171 | Common:4; Rare:94; Clinvar:1 | ||||
| chr4:158672226-158672326 | Rare:22; Clinvar:1 | ||||
| chr4:164977568-164977714 | Rare:38 | ||||
| chr4:168318734-168318856 | Rare:25 | ||||
| chr4:168480477-168480576 | Rare:13 | ||||
| chr4:169010223-169010456 | Common:1; Rare:69 | ||||
| chr4:169620400-169620690 | Common:2; Rare:102 | ||||
| chr4:173370690-173371012 | Common:2; Rare:82 | ||||
| chr4:174283631-174283938 | Common:1; Rare:57 | ||||
| chr4:177442353-177442514 | Rare:96; Clinvar:2; Clinvar (pathogenic):1 |