| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119018280-119018808 | Common:13; Rare:203 | ||||
| chr11:119057120-119057446 | Common:3; Rare:129 | ||||
| chr11:119067624-119067821 | Common:3; Rare:65 | ||||
| chr11:119095408-119095764 | Common:3; Rare:120 | ||||
| chr11:119101777-119102055 | Rare:73; Clinvar:4 | ||||
| chr11:119206180-119206335 | Common:5; Rare:73; Clinvar:6; Clinvar (benign):4 | ||||
| chr11:119334283-119334555 | Rare:73 | ||||
| chr11:120336314-120336556 | Rare:98 | ||||
| chr11:123062062-123062336 | Common:5; Rare:118 | ||||
| chr11:123062393-123062666 | Common:4; Rare:129 | ||||
| chr11:124673710-124673952 | Common:5; Rare:70 | ||||
| chr11:124800402-124800454 | Rare:17 | ||||
| chr11:124953964-124954213 | Common:5; Rare:73 | ||||
| chr11:125592510-125592913 | Common:6; Rare:131 | ||||
| chr11:125625850-125626003 | Rare:52 |