| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74060200-74060501 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):4 | ||||
| chr7:74062235-74062345 | Rare:20 | ||||
| chr7:74480491-74480664 | Common:2; Rare:43 | ||||
| chr7:74688891-74689221 | Rare:67 | ||||
| chr7:74700337-74700665 | Common:1; Rare:67 | ||||
| chr7:74726504-74726789 | Common:2; Rare:38 | ||||
| chr7:74890496-74890833 | Common:4; Rare:110 | ||||
| chr7:75359011-75359306 | Common:2; Rare:15 | ||||
| chr7:75410239-75410362 | Rare:10 | ||||
| chr7:75415638-75415740 | Rare:45 | ||||
| chr7:75415855-75416410 | Common:2; Rare:223 | ||||
| chr7:75639183-75639342 | Common:1; Rare:32 | ||||
| chr7:76063320-76063588 | Common:1; Rare:57 | ||||
| chr7:76304182-76304418 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:76571955-76572035 | Rare:9 |