| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44104120-44104356 | Common:2; Rare:27 | ||||
| chr7:44200856-44201067 | Common:2; Rare:72 | ||||
| chr7:44573891-44574047 | Common:3; Rare:44 | ||||
| chr7:44582170-44582428 | Common:1; Rare:90 | ||||
| chr7:44606459-44606632 | Common:1; Rare:60 | ||||
| chr7:44748343-44748577 | Common:2; Rare:61 | ||||
| chr7:44796397-44796784 | Common:3; Rare:149 | ||||
| chr7:45111662-45111822 | Common:1; Rare:61 | ||||
| chr7:50450322-50450453 | Common:1; Rare:54 | ||||
| chr7:56051424-56051851 | Common:1; Rare:164; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:66114754-66114889 | Common:1; Rare:68 | ||||
| chr7:66682024-66682179 | Common:5; Rare:76 | ||||
| chr7:73683437-73683617 | Common:2; Rare:72 | ||||
| chr7:73738793-73739109 | Common:2; Rare:98 | ||||
| chr7:74174104-74174386 | Common:1; Rare:145 |