| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062062-123062358 | Common:5; Rare:128 | ||||
| chr11:123062397-123062672 | Common:4; Rare:126 | ||||
| chr11:123741603-123741752 | Common:1; Rare:41 | ||||
| chr11:124673706-124673934 | Common:4; Rare:71 | ||||
| chr11:124762256-124762401 | Rare:38 | ||||
| chr11:124800406-124800461 | Rare:18 | ||||
| chr11:124953989-124954225 | Common:4; Rare:63 | ||||
| chr11:125164494-125164754 | Rare:50 | ||||
| chr11:125569245-125569572 | Common:2; Rare:96 | ||||
| chr11:125592499-125592933 | Common:6; Rare:141 | ||||
| chr11:125625875-125626003 | Rare:43 | ||||
| chr11:125887480-125887745 | Common:2; Rare:87 | ||||
| chr11:125903183-125903327 | Rare:33 | ||||
| chr11:126211641-126211809 | Rare:77 | ||||
| chr11:126268724-126269214 | Common:2; Rare:189; Clinvar:3; Clinvar (benign):4 |