chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3111479210111479211CA21GENIChomozygous112005068
3111479465111479466AG21GENIChomozygous112005070
3111482312111482313GA28GENIChomozygous112005074
3111483361111483362GA19GENIChomozygous111674763
3111483447111483448GA21GENIChomozygous112005076
3111489337111489338TC27GENIChomozygous112005082
3111491198111491199TC17GENIChomozygous119651132
3111493544111493545GA10GENIChomozygous111674765
3111494613111494614GA29GENIChomozygous112005086
3111495862111495863TC24GENIChomozygous112005088
3111498680111498681AG30GENIChomozygous111674767
3111499825111499826GT25GENIChomozygous111674769
3111502955111502956GA21GENIChomozygous112005092
3111506492111506493TC26GENIChomozygous111674771
3111513370111513371AG20GENIChomozygous112005094
3111515220111515221CT30GENIChomozygous112005096
3111516442111516443TC17GENIChomozygous112005098
3111518380111518381AG24GENIChomozygous112005100
3111527620111527621GA22GENIChomozygous112005108
3111527628111527629GC22GENIChomozygous112005110
3111528335111528336CT28GENIChomozygous112005112
3111528481111528482AG31GENIChomozygous112005114
3111528594111528595AG24GENIChomozygous112005116
3111528728111528729AT21GENIChomozygous112005118
3111530367111530368AG20GENIChomozygous112005120
3111531532111531533GA28GENICpossibly homozygous112005122
3111532622111532623CT41GENIChomozygous111674781
3111533432111533433GT27GENIChomozygous112005124
3111533435111533436TC26GENIChomozygous112005126
3111533683111533684AG37GENIChomozygous112005128
3111536654111536655GA24GENIChomozygous112005132
3111536979111536980TC30GENIChomozygous111674782