| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30465665-30465807 | Rare:18 | ||||
| chr7:30476476-30476784 | Rare:47 | ||||
| chr7:30561522-30561861 | Common:5; Rare:50 | ||||
| chr7:32728590-32728849 | Common:7; Rare:83 | ||||
| chr7:32942514-32942648 | Common:1; Rare:39 | ||||
| chr7:38335581-38335647 | Common:1; Rare:6 | ||||
| chr7:42888661-42888973 | Common:1; Rare:68 | ||||
| chr7:43623573-43623813 | Common:1; Rare:60 | ||||
| chr7:44019117-44019389 | Common:2; Rare:97 | ||||
| chr7:44105302-44105653 | Common:6; Rare:45 | ||||
| chr7:44107915-44108084 | Common:2; Rare:59; Clinvar (pathogenic):1 | ||||
| chr7:44112286-44112593 | Common:4; Rare:76 | ||||
| chr7:44467554-44467880 | Common:3; Rare:63 | ||||
| chr7:44801135-44801315 | Common:3; Rare:49 | ||||
| chr7:44986577-44986765 | Common:3; Rare:90 |