| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:93890710-93890909 | Common:3; Rare:47 | ||||
| chr7:93921344-93922068 | Common:5; Rare:140 | ||||
| chr7:94655995-94656381 | Common:2; Rare:107; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:95396119-95396275 | Common:2; Rare:53 | ||||
| chr7:95396276-95396538 | Common:3; Rare:117 | ||||
| chr7:95396724-95397126 | Common:4; Rare:70 | ||||
| chr7:95434861-95435225 | Common:1; Rare:135; Clinvar (benign):1 | ||||
| chr7:95435232-95435413 | Rare:23 | ||||
| chr7:95596507-95596682 | Common:2; Rare:34 | ||||
| chr7:96322020-96322241 | Rare:91; Clinvar:4 | ||||
| chr7:96709689-96709899 | Common:1; Rare:77 | ||||
| chr7:97872109-97872166 | Rare:20 | ||||
| chr7:98106839-98106898 | Rare:21 | ||||
| chr7:98252121-98252372 | Common:1; Rare:56 | ||||
| chr7:98306422-98306443 | Rare:7 |