| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44606808-44607120 | Common:3; Rare:93 | ||||
| chr7:44748423-44748602 | Rare:42 | ||||
| chr7:44796380-44796693 | Common:2; Rare:115 | ||||
| chr7:44799217-44799478 | Common:3; Rare:72 | ||||
| chr7:44847969-44848496 | Common:4; Rare:157 | ||||
| chr7:44999598-44999777 | Common:4; Rare:64 | ||||
| chr7:44999917-45000354 | Common:1; Rare:108; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:45111629-45111809 | Common:1; Rare:70 | ||||
| chr7:45574115-45574402 | Rare:51 | ||||
| chr7:47582065-47582335 | Common:1; Rare:79 | ||||
| chr7:47582543-47582685 | Rare:36 | ||||
| chr7:47979488-47979673 | Rare:81 | ||||
| chr7:48089030-48089270 | Common:3; Rare:61 | ||||
| chr7:48089404-48089648 | Common:2; Rare:59 | ||||
| chr7:50450296-50450481 | Common:1; Rare:86 |