Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:12046288-12046580 | Common:3; Rare:53 | ||||
chr11:12086652-12086871 | Common:2; Rare:36 | ||||
chr11:19714543-19714646 | Common:1; Rare:19 | ||||
chr11:19714748-19715068 | Common:1; Rare:74 | ||||
chr11:28702410-28702690 | Rare:50 | ||||
chr11:35623765-35623939 | Common:2; Rare:35 | ||||
chr11:57778538-57778834 | Rare:54 | ||||
chr11:64361513-64361678 | Rare:44 | ||||
chr11:65418705-65418929 | Common:2; Rare:45 | ||||
chr11:65421125-65421465 | Rare:73 | ||||
chr11:65422568-65422828 | Common:2; Rare:78 | ||||
chr11:65455103-65455290 | Rare:87 | ||||
chr11:65505336-65505390 | Common:1; Rare:22 | ||||
chr11:65526000-65526276 | Rare:94; Clinvar (pathogenic):1 | ||||
chr11:65891187-65891264 | Common:1; Rare:20 |