| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75914908-75915168 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994528-75994791 | Common:4; Rare:139 | ||||
| chr7:76047932-76048194 | Common:2; Rare:90 | ||||
| chr7:76302442-76302715 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:76302866-76303073 | Rare:87; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:76303461-76303821 | Common:2; Rare:155; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:77122287-77122689 | Common:2; Rare:80 | ||||
| chr7:77199775-77199935 | Rare:38 | ||||
| chr7:77696122-77696465 | Common:1; Rare:124 | ||||
| chr7:77697081-77697164 | Common:1; Rare:24 | ||||
| chr7:77798379-77798980 | Common:1; Rare:144 | ||||
| chr7:79452709-79453054 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr7:79453070-79453198 | Rare:32; Clinvar (benign):1 | ||||
| chr7:79453473-79453519 | Rare:11 | ||||
| chr7:79453538-79453584 | Rare:8 |