chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165973056165973057GC20GENIChomozygous108355825
1165974802165974803GA23GENIChomozygous108355826
1165976795165976796TG34GENIChomozygous108355831
1165978191165978192CA23GENIChomozygous108355833
1165978787165978788AT16GENIChomozygous108355834
1165981927165981928AT18GENIChomozygous108355839
1165984094165984095CT28GENIChomozygous108954609
1165984199165984200AG34GENIChomozygous108355846
1165986130165986131TC26GENIChomozygous108355852
1165990503165990504CT29GENIChomozygous108355871
1165993655165993656GA38GENIChomozygous108355875
1165993661165993662AG34GENIChomozygous108355876
1165994048165994049AG31GENIChomozygous108954617
1165994198165994199CT16GENIChomozygous108954618
1165995067165995068CT14GENIChomozygous120509143
1165995487165995488CT26GENIChomozygous108954620
1165987105165987106GA28GENIChomozygous120729704
1165990777165990778GA25GENIChomozygous120729706
1165992939165992940GA24GENIChomozygous120729708
1166005455166005456TC21GENIChomozygous108355886
1166005705166005706GA26GENIChomozygous109163018
1166007678166007679AG18GENIChomozygous108355889
1166007774166007775GT26GENICpossibly homozygous109163020