| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73005819-73006148 | Rare:38 | ||||
| chr7:73201971-73202140 | Rare:4 | ||||
| chr7:74223875-74224160 | Common:1; Rare:73 | ||||
| chr7:74890513-74890812 | Common:3; Rare:95 | ||||
| chr7:75162911-75163021 | Common:1; Rare:42 | ||||
| chr7:75358976-75359270 | Common:1; Rare:13 | ||||
| chr7:75410266-75410362 | Rare:3 | ||||
| chr7:75415817-75415915 | Rare:9 | ||||
| chr7:75415943-75416326 | Common:1; Rare:172 | ||||
| chr7:75639167-75639348 | Common:1; Rare:39 | ||||
| chr7:75979351-75979508 | Common:1; Rare:57 | ||||
| chr7:76304182-76304376 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:76571977-76572138 | Rare:23 | ||||
| chr7:76582946-76583138 | Common:1; Rare:27 | ||||
| chr7:76591619-76591657 | Rare:7 |