| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44200846-44201067 | Common:2; Rare:75 | ||||
| chr7:44573858-44574092 | Common:3; Rare:84 | ||||
| chr7:44582169-44582435 | Common:1; Rare:91 | ||||
| chr7:44606433-44606632 | Common:1; Rare:69 | ||||
| chr7:44606789-44607062 | Common:2; Rare:84 | ||||
| chr7:44748309-44748591 | Common:2; Rare:68 | ||||
| chr7:44796388-44796790 | Common:3; Rare:155 | ||||
| chr7:44999991-45000324 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr7:45111665-45111806 | Common:1; Rare:53 | ||||
| chr7:45888258-45888495 | Rare:40 | ||||
| chr7:45888930-45889263 | Common:4; Rare:74 | ||||
| chr7:47979507-47979765 | Common:1; Rare:100 | ||||
| chr7:48088909-48089269 | Common:6; Rare:94 | ||||
| chr7:50450309-50450467 | Common:1; Rare:71 | ||||
| chr7:50565367-50565521 | Rare:33 |