chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143554079135540792AG15GENIChomozygous113672877
143554079235540793GT15GENIChomozygous113672879
143554317935543179T9GENIChomozygous129145690
143554322335543224G16GENIChomozygous129145691
143554335935543360A17GENIChomozygous129145692
143554336235543363G17GENIChomozygous129145693
143554336735543369AT16GENIChomozygous129145694
143554337335543375TG15GENIChomozygous129145695
143555088635550887TC8GENICheterozygous133685897
143555089335550894CT4GENICheterozygous133685898
143555089535550896CT4GENICheterozygous133685899
143555393735553937G6GENIChomozygous129145701
143555395935553960AG9GENIChomozygous113818121
143555396035553961GA9GENIChomozygous114163610
143555397935553980C9GENIChomozygous129145702
143555400235554002TCAGCA9GENIChomozygous129145703
143555400735554010TGT9GENIChomozygous129145704
143555401135554012TA9GENIChomozygous113585709
143555401135554011C9GENIChomozygous129145705
143555401335554014TG9GENIChomozygous113585711
143555401535554016TC8GENIChomozygous113585713
143556366035563661GT16GENICpossibly homozygous113421899