| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44606459-44606653 | Common:1; Rare:64 | ||||
| chr7:44606812-44607055 | Common:2; Rare:70 | ||||
| chr7:44748307-44748591 | Common:2; Rare:69 | ||||
| chr7:44796384-44796790 | Common:3; Rare:158 | ||||
| chr7:44999555-44999747 | Common:4; Rare:68 | ||||
| chr7:44999991-45000315 | Common:1; Rare:76 | ||||
| chr7:45111652-45111816 | Common:1; Rare:64 | ||||
| chr7:45888170-45888507 | Rare:53 | ||||
| chr7:45888645-45889001 | Common:1; Rare:125 | ||||
| chr7:47582059-47582335 | Common:1; Rare:80 | ||||
| chr7:47979490-47979747 | Rare:95 | ||||
| chr7:48089039-48089245 | Common:1; Rare:51 | ||||
| chr7:50450309-50450453 | Common:1; Rare:59 | ||||
| chr7:56034113-56034222 | Rare:25 | ||||
| chr7:56051405-56051952 | Common:1; Rare:197; Clinvar:5; Clinvar (benign):1 |