chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266422220266422221GA28GENIChomozygous108638044
1266422600266422601AC25GENIChomozygous108638045
1266422930266422931CT31GENIChomozygous108638046
1266423134266423135TC27GENIChomozygous108638047
1266423372266423373TG7GENIChomozygous125327551
1266423463266423464CT16GENIChomozygous108638048
1266424165266424166CT28GENIChomozygous108638049
1266424638266424639GC31GENIChomozygous108638050
1266424690266424691GA26GENIChomozygous108638051
1266425164266425165TG30GENIChomozygous108638052
1266425367266425368AG28GENIChomozygous108638053
1266425809266425810CA31GENIChomozygous108638054
1266425994266425995TC25GENIChomozygous108638055
1266426008266426009CT25GENIChomozygous108638056
1266426009266426010GT26GENIChomozygous108638057
1266426479266426480AG18GENIChomozygous108638058
1266426538266426539GA16GENIChomozygous108638059
1266426608266426609GT20GENICpossibly homozygous108638060
1266428301266428302AG21GENIChomozygous108638061
1266428493266428494TC16GENIChomozygous108638062
1266429181266429182CT25GENIChomozygous108638063
1266429422266429423GA20GENIChomozygous108638064
1266429453266429454GA16GENIChomozygous108638065
1266429822266429823TC25GENIChomozygous108638066
1266429923266429924TC21GENIChomozygous108638067
1266427600266427600GTATCACAGAGG19GENIChomozygous127509137
1266429585266429586A25GENIChomozygous127509138