chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106219267262192673GA27GENIChomozygous116613496
106219304762193048CT25GENIChomozygous116939609
106219454862194549GT18GENIChomozygous116939611
106219597962195980AG23GENIChomozygous116613498
106219640762196408GA31GENIChomozygous116939613
106219678362196784TC32GENIChomozygous116939615
106219933262199333GC26GENIChomozygous116939617
106220018462200185AG8GENICheterozygous117061898
106220018862200189AT8GENICheterozygous117061900
106220041062200411TA15GENIChomozygous116613508
106220168862201689GA33GENIChomozygous116939619
106220281462202815AG25GENIChomozygous116613510
106220806262208063AG35GENIChomozygous116939621
106220886762208868TC21GENIChomozygous116613514
106220951762209518CT20GENIChomozygous116939623
106221072062210721CT31GENIChomozygous116613516
106221075962210760GA28GENIChomozygous116939625
106221258662212587AG21GENIChomozygous116613518
106221426062214261GT12GENICpossibly homozygous117061915
106222042562220426AG29GENIChomozygous116613526
106222069062220691CT28GENIChomozygous116613528
106222647062226471AG21GENIChomozygous116613542
106223189762231898TA30GENIChomozygous116613548
106223274662232747TC22GENIChomozygous116613556
106223593362235934GA25GENIChomozygous116939627
106223762262237623GA20GENIChomozygous116939629