| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:149873840-149874048 | Common:3; Rare:83 | ||||
| chr7:150567291-150567428 | Rare:20 | ||||
| chr7:150993546-150993806 | Common:1; Rare:66 | ||||
| chr7:151028149-151028471 | Rare:106 | ||||
| chr7:151080769-151080962 | Rare:57 | ||||
| chr7:151227166-151227411 | Common:1; Rare:67 | ||||
| chr7:151736463-151736671 | Common:1; Rare:33 | ||||
| chr7:155644377-155644720 | Common:2; Rare:118 | ||||
| chr7:156640555-156640770 | Common:2; Rare:101 | ||||
| chr7:157336936-157337085 | Common:1; Rare:69; Clinvar:2 | ||||
| chr7:158704740-158704986 | Common:1; Rare:86 | ||||
| chr7:158856518-158856666 | Common:6; Rare:61 | ||||
| chr8:232194-232377 | Common:2; Rare:69 | ||||
| chr8:6406518-6406680 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563000-6563021 | Common:1; Rare:6 |