chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103636217436362175TC8GENIChomozygous116759049
103636313336363134AG9GENIChomozygous116560613
103636323936363240TC5GENIChomozygous116560617
103636392236363923TC16GENIChomozygous116759051
103636478936364790AG10GENIChomozygous116560619
103636554536365546CT8GENIChomozygous116759053
103636568836365689TC8GENIChomozygous116759055
103636572036365721CT11GENIChomozygous116560625
103636593836365939AG7GENIChomozygous116560627
103636656536366566AG3GENIChomozygous116759057
103636726236367263AG11GENIChomozygous116759059
103636787236367873TC18GENIChomozygous116560629
103636797436367975CT10GENIChomozygous116759061
103636832436368325AG13GENIChomozygous116759063
103636841336368414TA10GENICheterozygous116560631
103636878736368788AG14GENIChomozygous116560635
103636964636369647TG11GENIChomozygous116759065
103637050536370506TA9GENIChomozygous116759067
103637073236370733CG9GENIChomozygous116759069
103637077236370773AG10GENIChomozygous116759071
103637222836372229CG9GENIChomozygous116759073
103637231836372319TC17GENIChomozygous116560639
103637240536372406GA16GENIChomozygous116759075
103637243836372439TC15GENIChomozygous116560641
103637247136372472TC13GENIChomozygous116560643
103637326836373269GA6GENIChomozygous116759077
103637329936373300AC5GENIChomozygous116759079
103637390136373902CT12GENIChomozygous116759081
103637397836373979TC17GENIChomozygous116759083
103637417936374180AG4GENIChomozygous116759085
103637429736374298GC16GENIChomozygous116759087
103637529936375300TA8GENIChomozygous116759089
103637541836375419GA8GENIChomozygous116759091
103637553536375536CG13GENIChomozygous116759093
103637609936376100GA8GENIChomozygous116759095
103637714436377145AG10GENIChomozygous116759097