| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56106387-56106661 | Common:7; Rare:100 | ||||
| chr7:64563063-64563267 | Common:3; Rare:51 | ||||
| chr7:66114750-66114919 | Common:1; Rare:79 | ||||
| chr7:66681973-66682179 | Common:5; Rare:92 | ||||
| chr7:66996557-66996872 | Common:2; Rare:73 | ||||
| chr7:73683429-73683622 | Common:3; Rare:77 | ||||
| chr7:73842506-73842693 | Common:6; Rare:27 | ||||
| chr7:74174031-74174386 | Common:1; Rare:161 | ||||
| chr7:74254351-74254620 | Rare:112 | ||||
| chr7:76047950-76048188 | Common:2; Rare:81 | ||||
| chr7:76302866-76303075 | Rare:87; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:77696236-77696481 | Rare:99 | ||||
| chr7:77798461-77798916 | Common:1; Rare:121 | ||||
| chr7:79453580-79453639 | Rare:20 | ||||
| chr7:79453659-79454106 | Common:3; Rare:107 |