| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44582154-44582463 | Common:1; Rare:113 | ||||
| chr7:44606471-44606635 | Common:1; Rare:57 | ||||
| chr7:44796361-44796787 | Common:3; Rare:164 | ||||
| chr7:45111665-45111806 | Common:1; Rare:53 | ||||
| chr7:50450309-50450453 | Common:1; Rare:59 | ||||
| chr7:56051405-56051837 | Common:1; Rare:161; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064145-56064329 | Common:2; Rare:107 | ||||
| chr7:64563078-64563267 | Common:3; Rare:45 | ||||
| chr7:65982196-65982328 | Common:1; Rare:35; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:66114813-66114889 | Common:1; Rare:37 | ||||
| chr7:66682005-66682184 | Common:5; Rare:88 | ||||
| chr7:66996569-66996850 | Common:2; Rare:57 | ||||
| chr7:73683419-73683628 | Common:3; Rare:86 | ||||
| chr7:73738779-73739144 | Common:2; Rare:118 | ||||
| chr7:74174140-74174412 | Common:1; Rare:143 |