chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266422220266422221GA24GENIChomozygous108638044
1266422600266422601AC21GENIChomozygous108638045
1266422930266422931CT27GENIChomozygous108638046
1266423134266423135TC22GENIChomozygous108638047
1266423372266423373TG9GENIChomozygous125327551
1266423463266423464CT25GENIChomozygous108638048
1266424165266424166CT12GENIChomozygous108638049
1266424638266424639GC24GENIChomozygous108638050
1266424690266424691GA16GENIChomozygous108638051
1266425164266425165TG15GENIChomozygous108638052
1266425367266425368AG18GENICpossibly homozygous108638053
1266425809266425810CA15GENIChomozygous108638054
1266425994266425995TC16GENIChomozygous108638055
1266426008266426009CT19GENIChomozygous108638056
1266426009266426010GT19GENIChomozygous108638057
1266426479266426480AG18GENIChomozygous108638058
1266426538266426539GA12GENIChomozygous108638059
1266426608266426609GT14GENICpossibly homozygous108638060
1266428301266428302AG21GENIChomozygous108638061
1266428493266428494TC14GENIChomozygous108638062
1266429181266429182CT18GENIChomozygous108638063
1266429422266429423GA17GENIChomozygous108638064
1266429453266429454GA15GENIChomozygous108638065
1266429822266429823TC19GENIChomozygous108638066
1266429923266429924TC20GENIChomozygous108638067
1266429585266429586A19GENIChomozygous127509138
1266427600266427600GTATCACAGAGG15GENIChomozygous127509137