chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157143793157143794TC17GENIChomozygous112905582
4157144099157144100CT15GENIChomozygous112905588
4157144997157144998TC19GENIChomozygous112905592
4157145222157145223CG19GENIChomozygous112905594
4157145282157145283GA19GENIChomozygous112905596
4157145362157145363TC26GENIChomozygous112905598
4157145639157145640AG30GENIChomozygous112905599
4157145756157145757GA16GENIChomozygous112905601
4157145862157145863GA14GENIChomozygous112905603
4157146025157146026AT16GENIChomozygous112905605
4157146155157146156GA6GENICheterozygous112905607
4157146176157146177TC7GENIChomozygous112905609
4157146181157146182AT8GENIChomozygous112905611
4157146453157146454TC7GENICheterozygous112905613
4157147329157147330TC17GENIChomozygous112905617
4157148213157148214GA18GENICpossibly homozygous112905619
4157148569157148570TG13GENIChomozygous112905621
4157148660157148661CT15GENIChomozygous112905623
4157150241157150242TA21GENIChomozygous126027595
4157153831157153832CT12GENIChomozygous112905642
4157153977157153978TC29GENIChomozygous112905644
4157154537157154538CA20GENIChomozygous112905646
4157154734157154735GC11GENIChomozygous126027596