| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:36510240-36510372 | Rare:37 | ||||
| chr11:43358858-43358957 | Rare:40 | ||||
| chr11:45917833-45918146 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46617201-46617279 | Rare:20 | ||||
| chr11:46700570-46700773 | Common:1; Rare:51 | ||||
| chr11:46846218-46846412 | Common:1; Rare:53 | ||||
| chr11:47176854-47177138 | Common:1; Rare:118 | ||||
| chr11:47269994-47270166 | Common:1; Rare:58 | ||||
| chr11:47565500-47565620 | Common:3; Rare:22 | ||||
| chr11:47578968-47579097 | Rare:65; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:57530682-57530802 | Rare:33 | ||||
| chr11:57712192-57712621 | Common:9; Rare:142 | ||||
| chr11:59107027-59107231 | Common:2; Rare:60 | ||||
| chr11:61333032-61333231 | Rare:67 | ||||
| chr11:61361874-61361957 | Common:1; Rare:17 |