| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43880980-43881100 | Common:1; Rare:18 | ||||
| chr11:46380550-46380888 | Common:1; Rare:97 | ||||
| chr11:46700567-46700812 | Common:1; Rare:62 | ||||
| chr11:46846258-46846422 | Common:1; Rare:48 | ||||
| chr11:47248783-47248947 | Rare:67 | ||||
| chr11:47578959-47579091 | Rare:66; Clinvar:2 | ||||
| chr11:57712198-57712617 | Common:9; Rare:137 | ||||
| chr11:59142736-59142926 | Common:1; Rare:34 | ||||
| chr11:60906433-60906801 | Rare:88 | ||||
| chr11:61295295-61295396 | Rare:23 | ||||
| chr11:61333032-61333275 | Common:1; Rare:90 | ||||
| chr11:61361809-61361973 | Common:1; Rare:40 | ||||
| chr11:61362098-61362404 | Common:2; Rare:90; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61429892-61430170 | Common:1; Rare:122; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:61792556-61792951 | Common:6; Rare:112 |