| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:43758560-43758721 | Common:1; Rare:31 | ||||
| chr7:43926373-43926457 | Rare:28 | ||||
| chr7:44573879-44574047 | Common:3; Rare:49 | ||||
| chr7:44582199-44582435 | Common:1; Rare:78 | ||||
| chr7:44606456-44606641 | Common:1; Rare:62 | ||||
| chr7:44748370-44748591 | Rare:50 | ||||
| chr7:44796500-44796692 | Common:1; Rare:68 | ||||
| chr7:44848100-44848479 | Common:2; Rare:97 | ||||
| chr7:44999555-44999759 | Common:4; Rare:71 | ||||
| chr7:44999913-45000210 | Common:1; Rare:62 | ||||
| chr7:45027410-45027724 | Common:2; Rare:69; Clinvar (benign):1 | ||||
| chr7:45111668-45111822 | Common:1; Rare:58 | ||||
| chr7:50304592-50304752 | Rare:31 | ||||
| chr7:55365919-55366076 | Rare:69 | ||||
| chr7:55366286-55366407 | Common:1; Rare:47 |