Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:62591489-62591837 | Rare:116 | ||||
chr11:62611507-62611841 | Rare:82 | ||||
chr11:62621949-62622234 | Common:2; Rare:87 | ||||
chr11:62646563-62646817 | Common:1; Rare:104; Clinvar (pathogenic):1 | ||||
chr11:62653262-62653440 | Common:1; Rare:60 | ||||
chr11:62665109-62665418 | Common:5; Rare:147 | ||||
chr11:62678864-62679144 | Rare:96 | ||||
chr11:62706217-62706463 | Common:3; Rare:102; Clinvar (benign):5 | ||||
chr11:62709497-62709705 | Common:1; Rare:91 | ||||
chr11:62727455-62727707 | Rare:93 | ||||
chr11:62727913-62728197 | Common:6; Rare:74 | ||||
chr11:62728418-62728581 | Common:2; Rare:96 | ||||
chr11:62753849-62753962 | Common:1; Rare:47 | ||||
chr11:62754138-62754386 | Common:1; Rare:55 | ||||
chr11:62761394-62761634 | Common:1; Rare:71 |