| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33257131-33257476 | Common:3; Rare:111 | ||||
| chr11:33722614-33722829 | Common:2; Rare:47 | ||||
| chr11:33736377-33736605 | Common:2; Rare:71 | ||||
| chr11:33774451-33774685 | Common:2; Rare:86 | ||||
| chr11:34051627-34051807 | Rare:73 | ||||
| chr11:34052122-34052499 | Common:4; Rare:171 | ||||
| chr11:34438769-34439009 | Common:2; Rare:81; Clinvar (benign):1 | ||||
| chr11:34620845-34621143 | Common:2; Rare:67 | ||||
| chr11:34622030-34622123 | Rare:10 | ||||
| chr11:34916292-34916671 | Common:10; Rare:154; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139398 | Common:1; Rare:124 | ||||
| chr11:35187306-35187338 | Rare:6 | ||||
| chr11:35197546-35197867 | Common:2; Rare:60 | ||||
| chr11:35200643-35200783 | Rare:24 | ||||
| chr11:35201056-35201279 | Common:2; Rare:63 |