| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118344268-118344407 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr11:118401351-118401699 | Rare:117 | ||||
| chr11:118527104-118527365 | Rare:35 | ||||
| chr11:118607577-118607647 | Common:1; Rare:14 | ||||
| chr11:118629824-118630073 | Common:1; Rare:51 | ||||
| chr11:118790875-118791305 | Rare:144 | ||||
| chr11:118997980-118998211 | Common:4; Rare:70 | ||||
| chr11:119018292-119018795 | Common:13; Rare:193 | ||||
| chr11:119057068-119057448 | Common:3; Rare:149 | ||||
| chr11:119067626-119067821 | Common:3; Rare:65 | ||||
| chr11:119095426-119095530 | Common:1; Rare:56 | ||||
| chr11:119101797-119101913 | Rare:35; Clinvar:1 | ||||
| chr11:119110624-119110953 | Rare:84 | ||||
| chr11:119111168-119111300 | Rare:29 | ||||
| chr11:119121371-119121635 | Common:1; Rare:62 |