Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61361819-61361973 | Common:1; Rare:39 | ||||
chr11:61362176-61362393 | Common:2; Rare:68; Clinvar:6; Clinvar (benign):1 | ||||
chr11:61429858-61430169 | Common:1; Rare:130; Clinvar:3; Clinvar (benign):5 | ||||
chr11:61792556-61792969 | Common:6; Rare:118 | ||||
chr11:61816134-61816256 | Rare:25 | ||||
chr11:61816960-61817038 | Rare:18 | ||||
chr11:61827944-61828303 | Common:1; Rare:71 | ||||
chr11:61967628-61967771 | Common:1; Rare:54; Clinvar:2 | ||||
chr11:61967821-61967887 | Rare:18 | ||||
chr11:62591515-62591837 | Rare:102 | ||||
chr11:62612458-62612746 | Common:4; Rare:75 | ||||
chr11:62621885-62622205 | Common:2; Rare:107 | ||||
chr11:62653282-62653504 | Common:1; Rare:56 | ||||
chr11:62665143-62665313 | Common:4; Rare:76 | ||||
chr11:62671745-62671965 | Common:1; Rare:87; Clinvar (benign):1 |