chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106219228662192287TA15GENIChomozygous116613494
106219267262192673GA17GENIChomozygous116613496
106219597962195980AG20GENIChomozygous116613498
106219656262196563GA15GENIChomozygous116613500
106219682062196821CG23GENIChomozygous116613502
106220008362200084AG22GENIChomozygous116613506
106220041062200411TA23GENIChomozygous116613508
106220281462202815AG20GENIChomozygous116613510
106220483862204839AG22GENIChomozygous116613512
106220886762208868TC26GENIChomozygous116613514
106221258662212587AG16GENIChomozygous116613518
106221333962213340AG16GENIChomozygous116613520
106221426562214266GT3GENICheterozygous126409447
106221852662218527TA7GENIChomozygous116613522
106221852762218528AT7GENIChomozygous116613524
106222001662220017AC10GENIChomozygous116890826
106222042562220426AG17GENIChomozygous116613526
106222069062220691CT24GENIChomozygous116613528
106222123062221231GC23GENIChomozygous116613530
106222134662221347CT8GENIChomozygous116613532
106222165062221651TA18GENIChomozygous116613536
106222192962221930AG8GENICheterozygous117997334
106222413762224138CT19GENIChomozygous116613538
106222613762226138GA30GENIChomozygous116613540
106222647062226471AG27GENIChomozygous116613542
106222690762226908TC12GENIChomozygous116613544
106223189762231898TA20GENIChomozygous116613548
106223223362232234GA12GENIChomozygous116613550
106223225662232257CG11GENICheterozygous116613552
106223227162232272GA16GENIChomozygous116613554
106223274662232747TC12GENIChomozygous116613556
106223327562233276AC5GENICheterozygous117061919
106223362562233626CT24GENIChomozygous116613558
106223464262234643CG22GENIChomozygous116613560
106223509862235099CT20GENIChomozygous116613562