| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74173926-74174441 | Common:3; Rare:194 | ||||
| chr7:74254366-74254535 | Rare:78 | ||||
| chr7:74453913-74454150 | Rare:66 | ||||
| chr7:74657456-74657788 | Common:2; Rare:92 | ||||
| chr7:74657924-74658067 | Common:1; Rare:33 | ||||
| chr7:75914957-75915164 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75981941-75982272 | Common:2; Rare:99; Clinvar:1 | ||||
| chr7:75983317-75983581 | Common:5; Rare:68; Clinvar (pathogenic):1 | ||||
| chr7:76047943-76048220 | Common:2; Rare:97 | ||||
| chr7:76302321-76302394 | Rare:18 | ||||
| chr7:76302513-76303075 | Common:3; Rare:232; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303665-76303865 | Common:1; Rare:90; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:76358768-76358905 | Rare:39 | ||||
| chr7:77122261-77122599 | Common:1; Rare:74 | ||||
| chr7:77199774-77199867 | Rare:26 |