| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062062-123062345 | Common:5; Rare:120 | ||||
| chr11:123062373-123062672 | Common:4; Rare:141 | ||||
| chr11:123063704-123063972 | Rare:63 | ||||
| chr11:123509787-123509960 | Rare:46 | ||||
| chr11:123654046-123654125 | Rare:14; Clinvar:3 | ||||
| chr11:123654331-123654784 | Common:6; Rare:118; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:123741561-123741807 | Common:2; Rare:70 | ||||
| chr11:124622561-124622946 | Common:7; Rare:115 | ||||
| chr11:124673716-124673940 | Common:4; Rare:65 | ||||
| chr11:124800103-124800485 | Common:1; Rare:133 | ||||
| chr11:124876588-124876862 | Common:2; Rare:54 | ||||
| chr11:124953926-124954213 | Common:5; Rare:87 | ||||
| chr11:125111506-125112032 | Common:4; Rare:128 | ||||
| chr11:125164607-125164826 | Rare:40 | ||||
| chr11:125451488-125451647 | Rare:37 |