chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4182465722182465723TG11GENIChomozygous112978737
4182466684182466685AC29GENIChomozygous112978738
4182466880182466881TG23GENIChomozygous112978740
4182476916182476917GA10GENIChomozygous112978754
4182477042182477043CA17GENIChomozygous112978756
4182482928182482929CA16GENIChomozygous112978765
4182484266182484267GA34GENIChomozygous112978772
4182491451182491452AC18GENIChomozygous112978807
4182491561182491562CG22GENIChomozygous112978809
4182491668182491669AC28GENIChomozygous112978810
4182491734182491735CA10GENIChomozygous112978812
4182491773182491774GT22GENIChomozygous112978813
4182534678182534679TG14GENIChomozygous112978960
4182534853182534854CT9GENIChomozygous112978962
4182534997182534998GC5GENIChomozygous112978964
4182535680182535681TG5GENIChomozygous112978967
4182535729182535730CA11GENIChomozygous112978968
4182535746182535747CA12GENIChomozygous112978970
4182535862182535863AG7GENIChomozygous112978972
4182536484182536485TC36GENIChomozygous112978973
4182497711182497712CT23GENICheterozygous113409485