| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:84194624-84194909 | Common:3; Rare:36 | ||||
| chr7:87152323-87152480 | Common:1; Rare:52 | ||||
| chr7:87345477-87345693 | Common:4; Rare:63 | ||||
| chr7:87876283-87876552 | Common:1; Rare:123 | ||||
| chr7:90245083-90245221 | Rare:40 | ||||
| chr7:90346602-90346736 | Common:3; Rare:58 | ||||
| chr7:92245857-92245970 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528439-92528807 | Common:3; Rare:112; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:94425766-94426050 | Rare:87; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94656114-94656424 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:98106747-98106907 | Common:1; Rare:44 | ||||
| chr7:98252197-98252365 | Rare:39 | ||||
| chr7:99408555-99408979 | Common:3; Rare:117 | ||||
| chr7:99438732-99438969 | Common:1; Rare:74 | ||||
| chr7:99558507-99558695 | Common:2; Rare:69 |