| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:43926382-43926489 | Rare:32 | ||||
| chr7:44044595-44044762 | Common:2; Rare:42 | ||||
| chr7:44200856-44201092 | Common:2; Rare:81 | ||||
| chr7:44573888-44574062 | Common:3; Rare:50 | ||||
| chr7:44582164-44582463 | Common:1; Rare:110 | ||||
| chr7:44606433-44606653 | Common:1; Rare:73 | ||||
| chr7:44606790-44607052 | Common:2; Rare:76 | ||||
| chr7:44748345-44748577 | Common:2; Rare:61 | ||||
| chr7:44796390-44796790 | Common:3; Rare:154 | ||||
| chr7:44797518-44797609 | Common:1; Rare:19 | ||||
| chr7:45111655-45111816 | Common:1; Rare:64 | ||||
| chr7:48088904-48089278 | Common:6; Rare:98 | ||||
| chr7:50450322-50450447 | Common:1; Rare:52 | ||||
| chr7:55572357-55572593 | Common:1; Rare:92 | ||||
| chr7:56051361-56051945 | Common:1; Rare:208; Clinvar:6; Clinvar (benign):1 |