| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44123502-44123776 | Common:4; Rare:81 | ||||
| chr7:44490607-44490937 | Rare:104 | ||||
| chr7:44573873-44574068 | Common:3; Rare:61 | ||||
| chr7:44582207-44582525 | Common:1; Rare:118 | ||||
| chr7:44606433-44606647 | Common:1; Rare:71 | ||||
| chr7:44606784-44607112 | Common:3; Rare:100 | ||||
| chr7:44759342-44759651 | Rare:75 | ||||
| chr7:44796384-44796692 | Common:2; Rare:112 | ||||
| chr7:44848172-44848462 | Common:2; Rare:72 | ||||
| chr7:44999457-44999769 | Common:4; Rare:92 | ||||
| chr7:44999977-45000357 | Common:1; Rare:88; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:45027495-45027724 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr7:45111677-45111822 | Common:1; Rare:53 | ||||
| chr7:50450319-50450493 | Common:1; Rare:87 | ||||
| chr7:55365918-55366052 | Rare:59 |