| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32583663-32583894 | Rare:86 | ||||
| chr11:33161431-33161678 | Common:6; Rare:70 | ||||
| chr11:33257157-33257479 | Common:3; Rare:107 | ||||
| chr11:33736404-33736591 | Common:1; Rare:62 | ||||
| chr11:33774501-33774670 | Common:2; Rare:62 | ||||
| chr11:34105478-34105718 | Common:2; Rare:80 | ||||
| chr11:34438785-34439016 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chr11:34916293-34916676 | Common:10; Rare:156; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35419546-35419685 | Rare:27 | ||||
| chr11:35525607-35525821 | Rare:46 | ||||
| chr11:35943965-35944087 | Common:2; Rare:43 | ||||
| chr11:36510229-36510372 | Rare:43 | ||||
| chr11:41459587-41459743 | Common:2; Rare:31 | ||||
| chr11:43311727-43312064 | Common:2; Rare:108 | ||||
| chr11:43358844-43358988 | Rare:68 |