| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152779724-152780013 | Common:1; Rare:81 | ||||
| chr4:158172360-158172633 | Rare:44 | ||||
| chr4:158172986-158173005 | Rare:4 | ||||
| chr4:158671830-158672313 | Common:5; Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723319-158723433 | Common:2; Rare:57 | ||||
| chr4:163166847-163167007 | Common:2; Rare:57 | ||||
| chr4:165327433-165327741 | Common:2; Rare:85 | ||||
| chr4:168318719-168318862 | Rare:29 | ||||
| chr4:169620415-169620725 | Common:2; Rare:105 | ||||
| chr4:173168250-173168286 | Common:1; Rare:6 | ||||
| chr4:173334280-173334731 | Rare:116 | ||||
| chr4:174283643-174283943 | Common:1; Rare:54 | ||||
| chr4:177442377-177442493 | Rare:70; Clinvar:1 | ||||
| chr4:177442495-177442518 | Rare:13; Clinvar:1 | ||||
| chr4:182917325-182917575 | Common:4; Rare:80 |