| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43358847-43358983 | Rare:65 | ||||
| chr11:44066183-44066530 | Common:3; Rare:90 | ||||
| chr11:44565281-44565687 | Common:3; Rare:100 | ||||
| chr11:45804290-45804425 | Common:1; Rare:30 | ||||
| chr11:45847221-45847521 | Common:2; Rare:128 | ||||
| chr11:45917816-45918004 | Rare:56; Clinvar:2 | ||||
| chr11:46120934-46121036 | Rare:9 | ||||
| chr11:46121056-46121291 | Common:2; Rare:43 | ||||
| chr11:46617136-46617600 | Common:5; Rare:131 | ||||
| chr11:46700549-46701077 | Common:4; Rare:133 | ||||
| chr11:46846218-46846416 | Common:1; Rare:56 | ||||
| chr11:47214837-47215110 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248785-47248938 | Rare:61 | ||||
| chr11:47269550-47269811 | Common:1; Rare:90 | ||||
| chr11:47269972-47270184 | Common:1; Rare:71 |