| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43880651-43880868 | Common:1; Rare:49 | ||||
| chr11:44066459-44066524 | Rare:17 | ||||
| chr11:45146318-45146481 | Common:1; Rare:28 | ||||
| chr11:45146605-45146660 | Rare:4 | ||||
| chr11:45804971-45805218 | Common:3; Rare:66; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45805321-45805424 | Rare:21; Clinvar:1 | ||||
| chr11:45917804-45917922 | Rare:35 | ||||
| chr11:46120936-46121296 | Common:2; Rare:56 | ||||
| chr11:46277600-46278209 | Common:1; Rare:150 | ||||
| chr11:46377789-46377930 | Rare:24 | ||||
| chr11:46380549-46380936 | Common:1; Rare:110 | ||||
| chr11:46593926-46594176 | Common:2; Rare:64 | ||||
| chr11:46617165-46617305 | Rare:35 | ||||
| chr11:46617774-46617926 | Rare:32 | ||||
| chr11:46681014-46681312 | Common:3; Rare:74 |