| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46381517-46381777 | Common:1; Rare:63 | ||||
| chr11:46617213-46617615 | Common:5; Rare:114 | ||||
| chr11:46700567-46700860 | Common:1; Rare:77 | ||||
| chr11:46700872-46701099 | Common:3; Rare:56 | ||||
| chr11:46846215-46846412 | Common:1; Rare:54 | ||||
| chr11:47248788-47248968 | Rare:74 | ||||
| chr11:47565478-47565620 | Common:3; Rare:28 | ||||
| chr11:47578941-47579327 | Rare:182; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:47638771-47639032 | Common:5; Rare:72 | ||||
| chr11:57324899-57325012 | Rare:32 | ||||
| chr11:57335832-57335953 | Common:1; Rare:23 | ||||
| chr11:57427075-57427214 | Common:1; Rare:44 | ||||
| chr11:57514839-57515021 | Common:1; Rare:38 | ||||
| chr11:57711973-57712621 | Common:10; Rare:212 | ||||
| chr11:57761687-57762018 | Common:1; Rare:57 |