| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92528403-92528807 | Common:3; Rare:124; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93890751-93890872 | Common:2; Rare:32 | ||||
| chr7:94425779-94426050 | Rare:84; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:94656114-94656380 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95596507-95596706 | Common:2; Rare:38 | ||||
| chr7:97024828-97025125 | Common:2; Rare:62 | ||||
| chr7:98878388-98878621 | Rare:84 | ||||
| chr7:99408545-99408690 | Common:2; Rare:48 | ||||
| chr7:99408818-99409018 | Common:1; Rare:64 | ||||
| chr7:99438710-99438985 | Common:1; Rare:90 | ||||
| chr7:99552069-99552182 | Rare:42 | ||||
| chr7:99558519-99558727 | Common:2; Rare:66 | ||||
| chr7:100088889-100088984 | Rare:30 | ||||
| chr7:100101365-100101661 | Common:1; Rare:108 | ||||
| chr7:100119341-100119728 | Rare:117 |