chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106219263462192635TC12GENICheterozygous116978456
106219267262192673GA13GENICheterozygous116613496
106219304762193048CT18GENIChomozygous116939609
106219454862194549GT25GENIChomozygous116939611
106219597962195980AG19GENIChomozygous116613498
106219640762196408GA10GENIChomozygous116939613
106219678362196784TC18GENIChomozygous116939615
106219933262199333GC16GENIChomozygous116939617
106220085962200860TC8GENIChomozygous118067752
106220168862201689GA27GENIChomozygous116939619
106220281462202815AG17GENIChomozygous116613510
106220806262208063AG16GENIChomozygous116939621
106220886762208868TC16GENIChomozygous116613514
106220951762209518CT12GENIChomozygous116939623
106221075962210760GA8GENIChomozygous116939625
106221258662212587AG15GENIChomozygous116613518
106222042562220426AG9GENICheterozygous116613526
106222069062220691CT28GENIChomozygous116613528
106222647062226471AG16GENIChomozygous116613542
106223189762231898TA12GENIChomozygous116613548
106223274662232747TC9GENIChomozygous116613556
106223327562233276AC5GENIChomozygous117061919
106223593362235934GA11GENIChomozygous116939627
106223762262237623GA7GENIChomozygous116939629
106222001662220017AC13GENIChomozygous116890826