chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1100787522100787523TC16GENIChomozygous61483700
1100787598100787599G-32GENIChomozygous61731891
1100787600100787601GA32GENICpossibly homozygous62146849
1100787893100787894AG21GENIChomozygous61483701
1100787941100787942CT13GENIChomozygous61731893
1100788109100788110CT27GENIChomozygous61483702
1100788274100788275CT26GENIChomozygous61731895
1100788323100788324GA31GENIChomozygous61731897
1100788398100788399CCCT27GENIChomozygous61483705
1100788402100788403TC24GENIChomozygous61483706
1100788504100788505AAC16GENIChomozygous61731899
1100790620100790621CT26GENIChomozygous61731901
1100791154100791155CA16GENIChomozygous61731903
1100791381100791393GTGTGTGTGTGT------------13GENICheterozygous62146851
1100791383100791393GTGTGTGTGT----------13GENICheterozygous62146853