| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:116526224-116526686 | Common:3; Rare:121; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:116671854-116672063 | Common:2; Rare:43 | ||||
| chr7:116672266-116672532 | Common:1; Rare:67; Clinvar:4 | ||||
| chr7:116953134-116953543 | Common:3; Rare:94 | ||||
| chr7:117872174-117872419 | Common:3; Rare:49 | ||||
| chr7:117873373-117873653 | Common:2; Rare:98 | ||||
| chr7:118183965-118184255 | Common:2; Rare:108 | ||||
| chr7:118214368-118214709 | Common:7; Rare:108 | ||||
| chr7:120857895-120858197 | Common:3; Rare:75; Clinvar:4 | ||||
| chr7:120950488-120950839 | Common:3; Rare:109 | ||||
| chr7:120951037-120951187 | Common:1; Rare:67 | ||||
| chr7:120988661-120988971 | Common:1; Rare:62 | ||||
| chr7:121396200-121396490 | Rare:91 | ||||
| chr7:122144178-122144451 | Common:1; Rare:58 | ||||
| chr7:123534537-123534877 | Common:6; Rare:75 |