| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062424-123062700 | Common:5; Rare:231 | ||||
| chr11:123741561-123741718 | Common:2; Rare:80 | ||||
| chr11:124622742-124622936 | Common:8; Rare:113 | ||||
| chr11:124673706-124673935 | Common:4; Rare:71 | ||||
| chr11:124762233-124762439 | Rare:91 | ||||
| chr11:124800365-124800491 | Common:1; Rare:84 | ||||
| chr11:124800604-124800720 | Common:1; Rare:24 | ||||
| chr11:124897779-124898021 | Common:4; Rare:55 | ||||
| chr11:124936288-124936423 | Rare:27 | ||||
| chr11:124953980-124954213 | Common:8; Rare:124 | ||||
| chr11:125063168-125063350 | Common:5; Rare:91 | ||||
| chr11:125111540-125112110 | Common:8; Rare:224 | ||||
| chr11:125569245-125569568 | Common:2; Rare:96 | ||||
| chr11:125592464-125592937 | Common:12; Rare:270; Clinvar (benign):1 | ||||
| chr11:125625450-125625790 | Common:2; Rare:159 |