| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67611919-67612238 | Common:2; Rare:121; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr11:68010174-68010360 | Common:1; Rare:47 | ||||
| chr11:68030437-68030744 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68036129-68036292 | Rare:49; Clinvar:1 | ||||
| chr11:68038919-68039101 | Rare:53; Clinvar:1 | ||||
| chr11:68049522-68049704 | Rare:59; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr11:68271855-68272160 | Common:2; Rare:122 | ||||
| chr11:68460223-68460516 | Common:3; Rare:95 | ||||
| chr11:68903753-68903954 | Common:5; Rare:92; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:69013174-69013276 | Common:3; Rare:26 | ||||
| chr11:69640837-69641243 | Common:1; Rare:88 | ||||
| chr11:69641364-69641508 | Rare:36 | ||||
| chr11:69675300-69675477 | Rare:51 | ||||
| chr11:70078395-70078679 | Rare:79 | ||||
| chr11:70165170-70165479 | Common:1; Rare:79 |