| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32165663-32165915 | Common:2; Rare:167 | ||||
| chr2:32265507-32265907 | Rare:90; Clinvar:1 | ||||
| chr2:32277759-32278019 | Common:4; Rare:124 | ||||
| chr2:32356909-32357259 | Common:8; Rare:290 | ||||
| chr2:32627932-32628180 | Rare:141 | ||||
| chr2:33599183-33599488 | Common:2; Rare:214 | ||||
| chr2:36355492-36356093 | Common:6; Rare:367 | ||||
| chr2:36356006-36356393 | Common:6; Rare:194 | ||||
| chr2:36966474-36966846 | Common:6; Rare:254 | ||||
| chr2:37084269-37084559 | Common:7; Rare:212 | ||||
| chr2:37156914-37157078 | Common:2; Rare:101 | ||||
| chr2:37231547-37231741 | Common:8; Rare:200; Clinvar:1; Clinvar (benign):7 | ||||
| chr2:37324675-37324911 | Common:2; Rare:167 | ||||
| chr2:37924710-37925120 | Common:9; Rare:204 | ||||
| chr2:37925140-37925395 | Common:4; Rare:183 |