| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3856207-3856277 | Rare:18 | ||||
| chr11:4094558-4095029 | Common:2; Rare:120 | ||||
| chr11:4393643-4393817 | Rare:44 | ||||
| chr11:4608125-4608416 | Common:1; Rare:92 | ||||
| chr11:5624881-5625033 | Rare:25 | ||||
| chr11:6234612-6234878 | Common:2; Rare:81 | ||||
| chr11:6259729-6259931 | Common:3; Rare:53 | ||||
| chr11:6319743-6319800 | Rare:16 | ||||
| chr11:6320490-6320599 | Common:2; Rare:35 | ||||
| chr11:6390225-6390562 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chr11:6473879-6474109 | Rare:71 | ||||
| chr11:6481276-6481569 | Common:5; Rare:131 | ||||
| chr11:6603454-6603880 | Common:4; Rare:133; Clinvar (benign):3 | ||||
| chr11:6604777-6604881 | Common:2; Rare:36 | ||||
| chr11:6612503-6612755 | Common:3; Rare:53 |