chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4114876914114876915TG19GENIChomozygous132972612
4114877357114877358AG22GENIChomozygous132972613
4114878211114878212TG15GENIChomozygous119441142
4114880701114880702GA23GENIChomozygous119441143
4114877889114877890GA23GENIChomozygous119441141
4114877846114877847TC17GENIChomozygous112813638
4114880429114880430AG19GENIChomozygous112813644
4114880981114880982TG24GENIChomozygous119441144
4114881333114881334TC23GENIChomozygous112813646
4114882551114882552GA22GENIChomozygous119441145
4114882762114882763CT13GENIChomozygous112813648
4114883005114883006GA23GENIChomozygous119441146
4114885947114885948CT14GENIChomozygous119441147
4114886050114886051GA16GENIChomozygous119441148
4114886296114886297TC18GENIChomozygous112813652
4114886526114886527GA16GENIChomozygous119441149
4114887625114887626GA23GENIChomozygous112813656
4114890305114890306CA1GENIChomozygous132972615
4114890918114890919AC20GENIChomozygous119441150
4114895981114895982CT21GENIChomozygous112813668
4114888660114888660C25GENIChomozygous132966768
4114883254114883254TCCC5GENIChomozygous132966767