| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44796397-44796769 | Common:3; Rare:147 | ||||
| chr7:44847981-44848269 | Common:3; Rare:91 | ||||
| chr7:45111642-45111767 | Common:1; Rare:58 | ||||
| chr7:47979508-47979726 | Rare:83 | ||||
| chr7:50093201-50093325 | Common:3; Rare:51 | ||||
| chr7:50450322-50450453 | Common:1; Rare:54 | ||||
| chr7:55365919-55366069 | Rare:67 | ||||
| chr7:55572341-55572653 | Common:1; Rare:114 | ||||
| chr7:56034137-56034234 | Rare:20 | ||||
| chr7:56051413-56051845 | Common:1; Rare:163; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56116361-56116513 | Common:1; Rare:34 | ||||
| chr7:64794267-64794441 | Common:3; Rare:51 | ||||
| chr7:66114768-66114895 | Common:1; Rare:64 | ||||
| chr7:66115194-66115353 | Rare:35 | ||||
| chr7:66682005-66682227 | Common:6; Rare:103 |