| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34916242-34916707 | Common:11; Rare:187; Clinvar:8; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35139012-35139201 | Common:1; Rare:38 | ||||
| chr11:35418990-35419043 | Rare:13 | ||||
| chr11:35419556-35419685 | Rare:24 | ||||
| chr11:35943942-35944131 | Common:2; Rare:65 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:41459596-41459691 | Rare:17 | ||||
| chr11:41460167-41460233 | Rare:15 | ||||
| chr11:43311727-43312053 | Common:2; Rare:105 | ||||
| chr11:43358834-43359012 | Rare:86 | ||||
| chr11:43680433-43680828 | Common:2; Rare:106 | ||||
| chr11:43880714-43880863 | Common:1; Rare:30 | ||||
| chr11:44066183-44066553 | Common:3; Rare:93 | ||||
| chr11:46120952-46121244 | Common:2; Rare:43 | ||||
| chr11:46277958-46278089 | Rare:36 |