| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:104917854-104917903 | Rare:11 | ||||
| chr7:104940907-104940964 | Common:1; Rare:20 | ||||
| chr7:104978199-104978308 | Rare:25 | ||||
| chr7:105012684-105012894 | Common:1; Rare:63 | ||||
| chr7:105013018-105013207 | Common:1; Rare:69 | ||||
| chr7:105013529-105013648 | Rare:42 | ||||
| chr7:105106955-105107222 | Rare:64 | ||||
| chr7:105111533-105111875 | Common:1; Rare:81 | ||||
| chr7:105373526-105373671 | Common:2; Rare:31 | ||||
| chr7:106011512-106011693 | Rare:37 | ||||
| chr7:107185602-107185908 | Common:1; Rare:77 | ||||
| chr7:107192456-107192818 | Common:1; Rare:64 | ||||
| chr7:107926270-107926584 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr7:107945548-107945583 | Rare:6 | ||||
| chr7:112110728-112110824 | Common:2; Rare:10 |