chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104671593146715932CT29GENIChomozygous116931532
104671669946716700GA20GENIChomozygous116931534
104671835646718357CT27GENIChomozygous116931536
104672066546720666GC14GENIChomozygous116586554
104672715646727157TC23GENIChomozygous116877908
104672882946728830AG14GENIChomozygous116586556
104673133046731331GA23GENIChomozygous116931538
104673384346733844CT25GENIChomozygous116931540
104673903546739036AG20GENIChomozygous116877914
104674047646740477CT8GENIChomozygous116931542
104674470546744706AG25GENIChomozygous116586564
104674504146745042TC26GENIChomozygous116586566
104674511346745114CG23GENIChomozygous116586568
104674915346749154AG19GENIChomozygous116586572
104674958346749584GT16GENIChomozygous116772948
104675068646750687TC20GENIChomozygous116586574
104675229646752297TC18GENIChomozygous116586576
104675347746753478AG20GENIChomozygous116772954
104675409846754099TC18GENIChomozygous116586578
104675585846755859AG22GENIChomozygous116772956
104675615746756158AG18GENIChomozygous116586580
104675755046757551AG24GENIChomozygous116586582
104676137146761372CT10GENIChomozygous116931544
104676144746761448TC23GENIChomozygous116586592