Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:50693505-50693619 | Rare:46 | ||||
chr16:50741708-50742204 | Common:7; Rare:155; Clinvar:1 | ||||
chr16:50742727-50742786 | Rare:10 | ||||
chr16:51151629-51151878 | Common:4; Rare:92 | ||||
chr16:53054788-53055089 | Common:2; Rare:65 | ||||
chr16:53434536-53434736 | Common:1; Rare:84 | ||||
chr16:53435492-53435700 | Common:1; Rare:42 | ||||
chr16:53703806-53704221 | Common:1; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
chr16:54286706-54287030 | Common:2; Rare:98 | ||||
chr16:55479037-55479207 | Rare:41 | ||||
chr16:55479417-55479626 | Common:1; Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
chr16:55508978-55509342 | Common:3; Rare:103 | ||||
chr16:55557313-55557450 | Rare:19 | ||||
chr16:56451274-56451605 | Common:1; Rare:105 | ||||
chr16:56608409-56609064 | Common:3; Rare:184 |