| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:150978492-150978559 | Common:1; Rare:11 | ||||
| chr7:151057892-151058205 | Common:3; Rare:77 | ||||
| chr7:151080776-151080959 | Rare:54 | ||||
| chr7:151632070-151632244 | Rare:67; Clinvar:4; Clinvar (benign):7 | ||||
| chr7:151736282-151736631 | Common:6; Rare:57 | ||||
| chr7:151877149-151877516 | Common:2; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:152025574-152025807 | Rare:92 | ||||
| chr7:155644357-155644724 | Common:2; Rare:129 | ||||
| chr7:156640535-156640685 | Common:3; Rare:78 | ||||
| chr7:157336770-157337149 | Common:3; Rare:176; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:158856414-158856716 | Common:7; Rare:105 | ||||
| chr7:159097007-159097399 | Common:1; Rare:83 | ||||
| chr8:232093-232377 | Common:3; Rare:107 | ||||
| chr8:1973826-1973910 | Rare:36 | ||||
| chr8:2127522-2127804 | Common:13; Rare:69 |