| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44606459-44606682 | Common:1; Rare:71 | ||||
| chr7:44606773-44607085 | Common:2; Rare:101 | ||||
| chr7:44748343-44748591 | Common:2; Rare:61 | ||||
| chr7:44796387-44796788 | Common:3; Rare:156 | ||||
| chr7:44999553-44999768 | Common:4; Rare:74 | ||||
| chr7:44999991-45000294 | Common:1; Rare:70 | ||||
| chr7:45111664-45111845 | Common:2; Rare:68 | ||||
| chr7:47539580-47539837 | Common:2; Rare:51 | ||||
| chr7:47581674-47581790 | Rare:27 | ||||
| chr7:47979507-47979753 | Rare:92 | ||||
| chr7:48089005-48089269 | Common:4; Rare:64 | ||||
| chr7:48089560-48089694 | Common:1; Rare:41 | ||||
| chr7:50450322-50450476 | Common:1; Rare:75 | ||||
| chr7:55018878-55019104 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:55365910-55366081 | Rare:72 |