| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62691078-62691282 | Common:1; Rare:67; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:62728412-62728522 | Common:2; Rare:66 | ||||
| chr11:62728658-62728836 | Rare:71 | ||||
| chr11:62787314-62787454 | Common:2; Rare:102 | ||||
| chr11:62791950-62792192 | Common:1; Rare:104 | ||||
| chr11:62832003-62832295 | Common:1; Rare:107 | ||||
| chr11:62855862-62856161 | Rare:116 | ||||
| chr11:63536775-63536853 | Rare:23 | ||||
| chr11:63974328-63974650 | Common:1; Rare:87 | ||||
| chr11:64166055-64166238 | Rare:52 | ||||
| chr11:64206597-64206798 | Common:1; Rare:47 | ||||
| chr11:64226081-64226339 | Common:3; Rare:74 | ||||
| chr11:64230183-64230619 | Common:3; Rare:150 | ||||
| chr11:64240888-64241175 | Rare:78 | ||||
| chr11:64251388-64251546 | Common:1; Rare:57 |