| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:43869464-43869669 | Rare:65 | ||||
| chr7:43926361-43926445 | Rare:30 | ||||
| chr7:44573888-44574077 | Common:3; Rare:59 | ||||
| chr7:44606397-44606643 | Common:1; Rare:86 | ||||
| chr7:44748352-44748577 | Common:2; Rare:59 | ||||
| chr7:44796387-44796790 | Common:3; Rare:156 | ||||
| chr7:45111676-45111816 | Common:1; Rare:52 | ||||
| chr7:50450329-50450447 | Rare:49 | ||||
| chr7:56051424-56051845 | Common:1; Rare:161; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106402-56106671 | Common:8; Rare:98 | ||||
| chr7:64563063-64563233 | Common:2; Rare:41 | ||||
| chr7:64665947-64666176 | Common:5; Rare:53 | ||||
| chr7:66114754-66114895 | Common:1; Rare:68 | ||||
| chr7:66682024-66682172 | Common:5; Rare:72 | ||||
| chr7:66996557-66996850 | Common:2; Rare:65 |