chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4168230035168230036TC40GENIChomozygous112943476
4168240034168240034GGAGGGAGGGAGGGAGGGAGGGAGGGAG12GENICpossibly homozygous129905447
4168241434168241435A32GENICheterozygous128102474
4168262086168262087AC35GENIChomozygous112943508
4168262632168262633A42GENICheterozygous132060627
4168265473168265474A41GENICheterozygous128102479
4168291957168291957A36GENIChomozygous128102487
4168292028168292028G43GENIChomozygous128102488
4168313769168313770TC37GENICheterozygous112943601
4168314075168314076AG17GENICheterozygous128140570
4168314244168314245GA10GENICheterozygous128140571
4168317020168317021AT31GENICheterozygous130307406
4168317020168317020T31GENICheterozygous133395938
4168317023168317025TT32GENICpossibly homozygous128102501
4168323574168323575G21GENIChomozygous128102504
4168323578168323579T21GENIChomozygous128102505
4168323591168323592A23GENIChomozygous128102506
4168323595168323596A23GENIChomozygous128102507
4168323596168323597GT23GENIChomozygous119283012