chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106219241962192420CA7GENIChomozygous123447922
106219267262192673GA25GENIChomozygous116613496
106219304762193048CT26GENIChomozygous116939609
106219454862194549GT23GENIChomozygous116939611
106219475562194755T13GENIChomozygous128822700
106219979862199799GC14GENIChomozygous116613504
106219597962195980AG22GENIChomozygous116613498
106219640762196408GA30GENIChomozygous116939613
106219678362196784TC19GENIChomozygous116939615
106219933262199333GC25GENIChomozygous116939617
106219640562196406G30GENIChomozygous131095408
106220041062200411TA18GENIChomozygous116613508
106220047762200481TTAT25GENIChomozygous128822701
106220085962200860TC27GENIChomozygous118067752
106220136762201367AG17GENIChomozygous128822702
106220168862201689GA18GENIChomozygous116939619
106220281462202815AG24GENIChomozygous116613510
106220806262208063AG18GENIChomozygous116939621
106220886762208868TC13GENIChomozygous116613514
106220951762209518CT19GENIChomozygous116939623
106221072062210721CT27GENIChomozygous116613516
106221075962210760GA25GENIChomozygous116939625
106221258662212587AG25GENIChomozygous116613518
106221426062214261GT13GENIChomozygous117061915
106221546962215469ATAA15GENICpossibly homozygous128822704
106221804962218057AAGAAAGG19GENIChomozygous128822705
106221940762219407A18GENICpossibly homozygous131095409
106222001662220017AC20GENIChomozygous116890826
106222004562220046CT21GENIChomozygous118067753
106222042562220426AG22GENIChomozygous116613526
106222069062220691CT19GENIChomozygous116613528
106222647062226471AG15GENIChomozygous116613542
106223189762231898TA18GENICpossibly homozygous116613548
106223274662232747TC24GENIChomozygous116613556
106223593362235934GA24GENIChomozygous116939627
106223762262237623GA21GENIChomozygous116939629
106220017662200176G4GENIChomozygous131465779