chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116671435066714351GA45GENIChomozygous970555111
116671589766715898GA30GENIChomozygous970555112
116671647966716480TC39GENIChomozygous970555113
116671668466716685GA32GENIChomozygous970555114
116671730866717309TA25GENIChomozygous970555115
116671760366717604GC22GENIChomozygous970555116
116671894366718944AG35GENIChomozygous970555117
116671931966719320AG21GENIChomozygous970555118
116672098466720985TA17GENIChomozygous970555119
116672164466721645TC29GENIChomozygous970555120
116672230266722303GA35GENIChomozygous970555121
116672248866722489TG36GENIChomozygous970555122
116672292266722923GT25GENIChomozygous970555123
116672350966723510TC41GENIChomozygous970555124
116672355566723556CT38GENIChomozygous970555125
116672411266724113AC18GENIChomozygous970555126
116672422866724229TC16GENIChomozygous970555127
116672424366724244CT17GENIChomozygous970555128
116672493366724934CG34GENIChomozygous970555129
116672502566725026CT26GENIChomozygous970555130
116672515966725160AG16GENIChomozygous970555131
116672543466725435TC17GENIChomozygous970555132
116672601466726015TG28GENIChomozygous970555133
116672636166726362TC18GENIChomozygous970555134
116672647966726480GA33GENIChomozygous970555135
116672675466726755GC32GENIChomozygous970555136
116672734666727347AG46GENIChomozygous970555137
116672886966728870AC19GENICheterozygous970555138
116672929066729291CT15GENIChomozygous970555139
116673084166730842GA41GENIChomozygous970555140
116673086366730864CT41GENIChomozygous970555141