| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74174114-74174396 | Common:1; Rare:148 | ||||
| chr7:74209832-74210021 | Rare:48 | ||||
| chr7:74254360-74254528 | Rare:79 | ||||
| chr7:75878805-75879083 | Common:12; Rare:100 | ||||
| chr7:75914908-75915164 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994507-75994772 | Common:4; Rare:133 | ||||
| chr7:76047943-76048180 | Common:1; Rare:81 | ||||
| chr7:76302501-76302675 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76302834-76303075 | Rare:103; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:76303456-76303744 | Common:2; Rare:114 | ||||
| chr7:76303761-76303831 | Rare:38; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:77122322-77122672 | Common:2; Rare:72 | ||||
| chr7:77199732-77199911 | Rare:50 | ||||
| chr7:77696127-77696518 | Common:1; Rare:156 | ||||
| chr7:77798363-77798956 | Common:1; Rare:143 |