chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91485434614854347GA22GENIChomozygous144842066
91485439314854394CT21GENIChomozygous144842067
91485453514854536CG22GENIChomozygous144842068
91485485014854851TC9GENIChomozygous142131675
91485485714854858TC8GENIChomozygous142131676
91485488214854883AG8GENIChomozygous138522594
91485500214855003TC22GENIChomozygous138522595
91485619514856196CG16GENIChomozygous142131677
91485638514856386CT19GENIChomozygous144842069
91485660114856602GA16GENIChomozygous144842070
91485720414857205CT8GENIChomozygous142131678
91485730114857302GA15GENIChomozygous144842071
91485805514858056TC19GENIChomozygous144842072
91485973414859735AC19GENIChomozygous142131680
91485998514859986TA21GENIChomozygous144842073
91486003614860041CTAGG19GENIChomozygous144834955
91486013314860134TC22GENIChomozygous144842074
91486089214860893CT17GENIChomozygous144842075
91486105514861056AG20GENIChomozygous144842076
91486190314861903T19GENIChomozygous142109676
91486242214862423AC9GENIChomozygous142131681
91486287914862880TC15GENIChomozygous142131682
91486567614865677AG15GENIChomozygous144842077
91486681114866812TG3GENIChomozygous144842078
91486709214867093CG19GENIChomozygous144842079
91486718414867185AT16GENIChomozygous144842080
91486793914867940TC18GENIChomozygous142131685
91486812214868123GC13GENIChomozygous142131686
91486831714868318AG24GENIChomozygous142131687
91486832514868326AG20GENIChomozygous142131688
91486856314868564TA16GENIChomozygous142131689
91486878014868781TC16GENIChomozygous144842081
91486905414869055T21GENIChomozygous142109677
91486908914869090CT18GENIChomozygous142131690