| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72112641-72112958 | Common:4; Rare:134 | ||||
| chr11:72223786-72223927 | Rare:41 | ||||
| chr11:72244170-72244445 | Rare:81 | ||||
| chr11:72308350-72308382 | Rare:2 | ||||
| chr11:72308454-72308471 | Rare:1 | ||||
| chr11:72308494-72309020 | Common:1; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:72358986-72359456 | Common:1; Rare:104; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:72434166-72434283 | Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:72674403-72674504 | Rare:22 | ||||
| chr11:72752387-72752602 | Common:3; Rare:61 | ||||
| chr11:72793599-72793806 | Common:1; Rare:51 | ||||
| chr11:72794028-72794217 | Rare:27 | ||||
| chr11:72814099-72814442 | Common:3; Rare:98 | ||||
| chr11:72822094-72822478 | Common:1; Rare:154 | ||||
| chr11:73141887-73141963 | Common:1; Rare:20 |