| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152779601-152780160 | Common:3; Rare:134 | ||||
| chr4:153204304-153204464 | Rare:34 | ||||
| chr4:154550365-154550523 | Rare:49 | ||||
| chr4:155376722-155376843 | Rare:38 | ||||
| chr4:155667221-155667415 | Rare:44 | ||||
| chr4:155667593-155667816 | Common:1; Rare:60 | ||||
| chr4:158210259-158210571 | Common:3; Rare:80 | ||||
| chr4:158671807-158672437 | Common:5; Rare:171; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723294-158723484 | Common:2; Rare:87 | ||||
| chr4:158768850-158769193 | Common:1; Rare:110 | ||||
| chr4:159103617-159103766 | Common:1; Rare:38 | ||||
| chr4:159103840-159104083 | Common:4; Rare:81 | ||||
| chr4:159227979-159228280 | Rare:63 | ||||
| chr4:159229213-159229466 | Common:2; Rare:42 | ||||
| chr4:163166832-163167015 | Common:2; Rare:71 |