chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106219267262192673GA34GENIChomozygous116613496
106219454862194549GT27GENIChomozygous116939611
106219597962195980AG15GENIChomozygous116613498
106219640762196408GA24GENIChomozygous116939613
106219678362196784TC31GENICpossibly homozygous116939615
106219933262199333GC29GENIChomozygous116939617
106220041062200411TA13GENIChomozygous116613508
106220168862201689GA18GENIChomozygous116939619
106220281462202815AG21GENIChomozygous116613510
106220806262208063AG28GENIChomozygous116939621
106220886762208868TC30GENIChomozygous116613514
106220951762209518CT19GENIChomozygous116939623
106221072062210721CT27GENIChomozygous116613516
106221075962210760GA26GENIChomozygous116939625
106221258662212587AG25GENIChomozygous116613518
106221426062214261GT13GENIChomozygous117061915
106221542062215421AC3GENICheterozygous117179670
106221542162215422AT3GENICheterozygous117179671
106221542262215423AT3GENICheterozygous117179672
106222042562220426AG12GENIChomozygous116613526
106222069062220691CT21GENIChomozygous116613528
106222647062226471AG27GENIChomozygous116613542
106223189762231898TA17GENIChomozygous116613548
106223274662232747TC21GENIChomozygous116613556
106223593362235934GA24GENIChomozygous116939627
106223762262237623GA22GENIChomozygous116939629