| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44606781-44607103 | Common:2; Rare:100 | ||||
| chr7:44748315-44748611 | Common:2; Rare:74 | ||||
| chr7:44796384-44796790 | Common:3; Rare:158 | ||||
| chr7:44978988-44979194 | Rare:36 | ||||
| chr7:44999607-44999751 | Common:2; Rare:55 | ||||
| chr7:44999984-45000295 | Common:1; Rare:70 | ||||
| chr7:45111665-45111806 | Common:1; Rare:53 | ||||
| chr7:47979483-47979756 | Rare:104 | ||||
| chr7:48088847-48089278 | Common:6; Rare:109 | ||||
| chr7:48089546-48089748 | Common:2; Rare:54 | ||||
| chr7:50450306-50450476 | Common:1; Rare:80 | ||||
| chr7:51316801-51317004 | Common:5; Rare:70 | ||||
| chr7:55018882-55019253 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:55365897-55366091 | Rare:81 | ||||
| chr7:55366263-55366393 | Common:1; Rare:51 |