| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73386182-73386326 | Common:1; Rare:54; Clinvar (benign):3 | ||||
| chr2:73737266-73737602 | Common:3; Rare:111 | ||||
| chr2:73828785-73829024 | Common:1; Rare:55 | ||||
| chr2:74002568-74002721 | Common:2; Rare:63 | ||||
| chr2:74147830-74148108 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178794-74179012 | Common:2; Rare:61 | ||||
| chr2:74198440-74198637 | Rare:78 | ||||
| chr2:74380267-74380547 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:74421628-74421753 | Rare:41 | ||||
| chr2:74440425-74440688 | Rare:69 | ||||
| chr2:74441847-74442030 | Common:2; Rare:43 | ||||
| chr2:74465336-74465455 | Common:1; Rare:32; Clinvar:1 | ||||
| chr2:74472363-74472750 | Common:4; Rare:177 | ||||
| chr2:74482928-74483113 | Common:1; Rare:67 | ||||
| chr2:74503031-74503150 | Rare:24 |