| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119018280-119018795 | Common:13; Rare:199 | ||||
| chr11:119057068-119057446 | Common:3; Rare:147 | ||||
| chr11:119067632-119067826 | Common:3; Rare:64 | ||||
| chr11:119101810-119101895 | Rare:26 | ||||
| chr11:119206191-119206367 | Common:5; Rare:78; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119317097-119317275 | Rare:59 | ||||
| chr11:120336198-120336577 | Rare:146 | ||||
| chr11:120336897-120337185 | Common:1; Rare:39 | ||||
| chr11:123062393-123062663 | Common:4; Rare:127 | ||||
| chr11:124673706-124673935 | Common:4; Rare:71 | ||||
| chr11:124762229-124762441 | Rare:57 | ||||
| chr11:124800405-124800491 | Common:1; Rare:35 | ||||
| chr11:124953989-124954135 | Common:3; Rare:42 | ||||
| chr11:125451449-125451625 | Rare:39 | ||||
| chr11:125592506-125592909 | Common:6; Rare:129 |