| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:116526181-116526683 | Common:3; Rare:139; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:116672171-116672468 | Common:1; Rare:66; Clinvar:2 | ||||
| chr7:116724487-116724783 | Common:2; Rare:69 | ||||
| chr7:116862383-116862649 | Common:2; Rare:97 | ||||
| chr7:116953170-116953536 | Common:3; Rare:85 | ||||
| chr7:117014834-117014964 | Rare:16 | ||||
| chr7:117020051-117020301 | Common:2; Rare:38 | ||||
| chr7:118183942-118184257 | Common:2; Rare:118 | ||||
| chr7:118214534-118214664 | Common:2; Rare:44 | ||||
| chr7:120950491-120950833 | Common:3; Rare:107 | ||||
| chr7:120951085-120951219 | Rare:48 | ||||
| chr7:120988594-120988872 | Rare:60 | ||||
| chr7:121396224-121396554 | Common:1; Rare:115 | ||||
| chr7:123534561-123534833 | Common:5; Rare:55 | ||||
| chr7:123557741-123557986 | Common:1; Rare:62 |