| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118359465-118359667 | Common:3; Rare:87 | ||||
| chr11:118401350-118401698 | Rare:116 | ||||
| chr11:118607361-118607638 | Common:1; Rare:43 | ||||
| chr11:118790894-118791259 | Rare:105 | ||||
| chr11:118791261-118791290 | Rare:19 | ||||
| chr11:118997977-118998200 | Common:4; Rare:70 | ||||
| chr11:119018280-119018457 | Common:6; Rare:72 | ||||
| chr11:119018626-119018800 | Common:5; Rare:73 | ||||
| chr11:119057127-119057460 | Common:3; Rare:133 | ||||
| chr11:119067632-119067826 | Common:3; Rare:64 | ||||
| chr11:119206180-119206325 | Common:5; Rare:67; Clinvar:6; Clinvar (benign):4 | ||||
| chr11:119311363-119311544 | Rare:66 | ||||
| chr11:119317097-119317303 | Rare:69 | ||||
| chr11:121292615-121292798 | Rare:61; Clinvar:3 | ||||
| chr11:123060114-123060560 | Common:7; Rare:147 |