| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46120943-46121028 | Rare:9 | ||||
| chr11:46382194-46382304 | Rare:38 | ||||
| chr11:46617215-46617572 | Common:5; Rare:100 | ||||
| chr11:46700553-46700818 | Common:1; Rare:69 | ||||
| chr11:46846224-46846389 | Rare:43 | ||||
| chr11:47214837-47214991 | Common:1; Rare:37 | ||||
| chr11:47248794-47248933 | Rare:55 | ||||
| chr11:47269348-47269684 | Common:3; Rare:93 | ||||
| chr11:47270018-47270166 | Common:1; Rare:52 | ||||
| chr11:47426406-47426632 | Rare:57 | ||||
| chr11:47565483-47565635 | Common:3; Rare:29 | ||||
| chr11:47578959-47579094 | Rare:69; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:57324902-57325125 | Common:1; Rare:69 | ||||
| chr11:57427075-57427216 | Common:1; Rare:45 | ||||
| chr11:57657486-57657790 | Common:4; Rare:80 |