| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66682030-66682185 | Common:5; Rare:72 | ||||
| chr7:66996550-66996865 | Common:3; Rare:69 | ||||
| chr7:72828180-72828482 | Rare:75 | ||||
| chr7:73557594-73557756 | Common:2; Rare:61 | ||||
| chr7:73683405-73683622 | Common:3; Rare:89 | ||||
| chr7:73738786-73739018 | Common:1; Rare:69 | ||||
| chr7:73842506-73842699 | Common:6; Rare:29 | ||||
| chr7:74173960-74174441 | Common:3; Rare:191 | ||||
| chr7:74254351-74254520 | Rare:77 | ||||
| chr7:75878847-75879083 | Common:12; Rare:86 | ||||
| chr7:75914944-75915164 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76047919-76048220 | Common:2; Rare:106 | ||||
| chr7:76302877-76303075 | Rare:83; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr7:77696216-77696471 | Rare:103 | ||||
| chr7:77798344-77798910 | Common:1; Rare:137 |