| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46120952-46121294 | Common:2; Rare:55 | ||||
| chr11:46277908-46278071 | Rare:43 | ||||
| chr11:46617198-46617578 | Common:5; Rare:108 | ||||
| chr11:46700857-46701099 | Common:3; Rare:62 | ||||
| chr11:46846224-46846422 | Common:1; Rare:57 | ||||
| chr11:47214840-47215011 | Common:1; Rare:43 | ||||
| chr11:47248794-47248919 | Rare:48 | ||||
| chr11:47270005-47270184 | Common:1; Rare:61 | ||||
| chr11:47426412-47426624 | Rare:52 | ||||
| chr11:47565517-47565646 | Common:2; Rare:24 | ||||
| chr11:47578968-47579113 | Rare:75; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47848317-47848653 | Common:3; Rare:118 | ||||
| chr11:57324890-57325173 | Common:1; Rare:87 | ||||
| chr11:57712175-57712621 | Common:9; Rare:148 | ||||
| chr11:58577477-58577764 | Rare:61 |