| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:39566306-39566440 | Common:1; Rare:66 | ||||
| chr7:39623503-39623812 | Rare:96 | ||||
| chr7:40134843-40135026 | Rare:65; Clinvar:1 | ||||
| chr7:42932116-42932418 | Rare:120 | ||||
| chr7:43869466-43869628 | Rare:52 | ||||
| chr7:43926378-43926457 | Rare:26 | ||||
| chr7:44044582-44044740 | Common:2; Rare:44 | ||||
| chr7:44200847-44201067 | Common:2; Rare:75 | ||||
| chr7:44573881-44574053 | Common:3; Rare:50 | ||||
| chr7:44606440-44606632 | Common:1; Rare:65 | ||||
| chr7:44748343-44748591 | Common:2; Rare:61 | ||||
| chr7:44796361-44796790 | Common:3; Rare:165 | ||||
| chr7:45111687-45111816 | Common:1; Rare:44 | ||||
| chr7:48088995-48089236 | Common:3; Rare:52 | ||||
| chr7:56051405-56051845 | Common:1; Rare:166; Clinvar:5; Clinvar (benign):1 |