| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:30322944-30323186 | Common:2; Rare:70 | ||||
| chr11:31509575-31509794 | Common:1; Rare:69 | ||||
| chr11:33161449-33161648 | Common:6; Rare:52 | ||||
| chr11:33257591-33257824 | Common:1; Rare:58 | ||||
| chr11:33258475-33258634 | Rare:54 | ||||
| chr11:33774484-33774685 | Common:2; Rare:71 | ||||
| chr11:34052138-34052451 | Common:4; Rare:149 | ||||
| chr11:34438796-34439009 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr11:34916287-34916709 | Common:10; Rare:173; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35662998-35663363 | Rare:117 | ||||
| chr11:36289378-36289747 | Common:3; Rare:98 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43880703-43880863 | Common:1; Rare:32 | ||||
| chr11:46361392-46361641 | Rare:55 | ||||
| chr11:46617165-46617585 | Common:5; Rare:118 |