| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358799-43358983 | Rare:88 | ||||
| chr11:43680455-43680822 | Common:1; Rare:102 | ||||
| chr11:43880699-43880875 | Common:2; Rare:37 | ||||
| chr11:44066183-44066272 | Common:1; Rare:27 | ||||
| chr11:45847175-45847487 | Common:2; Rare:123 | ||||
| chr11:46617165-46617572 | Common:5; Rare:117 | ||||
| chr11:46700555-46700796 | Common:1; Rare:65 | ||||
| chr11:46846211-46846421 | Common:1; Rare:60 | ||||
| chr11:47176837-47177152 | Common:1; Rare:131 | ||||
| chr11:47214326-47214488 | Common:1; Rare:19 | ||||
| chr11:47214837-47215124 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248794-47248957 | Rare:66 | ||||
| chr11:47269330-47269375 | Rare:10 | ||||
| chr11:47269556-47269811 | Common:1; Rare:89 |