| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107744022-107744170 | Rare:44 | ||||
| chr7:107929077-107929496 | Common:2; Rare:123; Clinvar:1 | ||||
| chr7:107929498-107929872 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:108526099-108526463 | Common:5; Rare:114 | ||||
| chr7:108569576-108570056 | Common:2; Rare:170 | ||||
| chr7:112206392-112206719 | Common:1; Rare:109 | ||||
| chr7:112450285-112450480 | Common:4; Rare:65 | ||||
| chr7:112790350-112790672 | Common:1; Rare:83 | ||||
| chr7:116499508-116499790 | Common:3; Rare:96 | ||||
| chr7:116525494-116525568 | Common:1; Rare:25 | ||||
| chr7:116526224-116526564 | Common:2; Rare:92; Clinvar:2 | ||||
| chr7:116672232-116672449 | Common:1; Rare:51; Clinvar:2 | ||||
| chr7:117322901-117323212 | Rare:79 | ||||
| chr7:117872161-117872407 | Common:3; Rare:50 | ||||
| chr7:118183964-118184229 | Common:2; Rare:101 |