| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:116250000-116250297 | Common:2; Rare:66 | ||||
| chr7:116499435-116499856 | Common:3; Rare:143 | ||||
| chr7:116499868-116500086 | Common:1; Rare:64 | ||||
| chr7:116526172-116526683 | Common:3; Rare:143; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:118183991-118184203 | Common:1; Rare:81 | ||||
| chr7:120950608-120950846 | Common:2; Rare:68 | ||||
| chr7:120951002-120951191 | Common:1; Rare:79 | ||||
| chr7:120988654-120988958 | Common:1; Rare:60 | ||||
| chr7:122144207-122144439 | Common:1; Rare:50 | ||||
| chr7:123534573-123534829 | Common:5; Rare:52 | ||||
| chr7:123748764-123749278 | Common:3; Rare:179 | ||||
| chr7:124929793-124930009 | Common:3; Rare:69 | ||||
| chr7:127585584-127585668 | Rare:27 | ||||
| chr7:127588207-127588508 | Rare:116 | ||||
| chr7:127651823-127652242 | Common:3; Rare:124 |