| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35943942-35944101 | Common:2; Rare:56 | ||||
| chr11:36510229-36510372 | Rare:43 | ||||
| chr11:40293159-40293375 | Common:1; Rare:48 | ||||
| chr11:41459455-41459693 | Common:1; Rare:45 | ||||
| chr11:43311713-43312047 | Common:2; Rare:106 | ||||
| chr11:43358831-43358983 | Rare:76 | ||||
| chr11:43880708-43880863 | Common:1; Rare:32 | ||||
| chr11:45917824-45918146 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46593997-46594121 | Common:1; Rare:24 | ||||
| chr11:46617201-46617594 | Common:5; Rare:109 | ||||
| chr11:46700568-46700979 | Common:3; Rare:92 | ||||
| chr11:46846198-46846437 | Common:1; Rare:70 | ||||
| chr11:47176837-47177126 | Common:1; Rare:120 | ||||
| chr11:47186408-47186542 | Rare:37 | ||||
| chr11:47214843-47214990 | Common:1; Rare:37 |