chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
648042604804261CG10GENIChomozygous55063139
648044434804444TTC5GENICheterozygous55063140
648044514804452AG3GENICheterozygous54278920
648044664804467AG7GENIChomozygous54278921
648045114804512TC13GENIChomozygous54278922
648049064804907GA21GENIChomozygous55063141
648053094805310CG19GENIChomozygous55063142
648054574805458AG22GENIChomozygous55063143
648056074805608GA19GENIChomozygous55063144
648060334806034CT22GENIChomozygous54278926
648062124806213TC21GENIChomozygous55063145
648068154806816AC18GENICpossibly homozygous54278927
648071104807111T-10GENIChomozygous54278928
648082174808218GC10GENICpossibly homozygous54278929
648084034808404GA11GENIChomozygous54278930
648088014808802CT19GENIChomozygous55063146
648089044808905GC9GENIChomozygous55063147
648092584809259TC11GENICpossibly homozygous54278932
648093764809377T-3GENIChomozygous54278933
648097144809715CCACAGG6GENIChomozygous54278934
648101094810110AC9GENIChomozygous54278935
648101164810117GA10GENICheterozygous54278936
648105384810539GA17GENICpossibly homozygous55063148
648111734811174TG8GENIChomozygous54278940
648111814811182CA8GENIChomozygous55063149
648114674811468TA25GENIChomozygous55063150
648140044814005GA2GENIChomozygous54278943
648142144814215GT19GENIChomozygous54278944
648145324814533GA30GENICpossibly homozygous54278945
648146364814637AG17GENIChomozygous54278946
648149794814980AT9GENICpossibly homozygous54278947
648153024815303CT11GENICheterozygous54278948
648153554815356CT14GENICpossibly homozygous54278950
648155744815575TA22GENIChomozygous55063151