chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266422220266422221GA18GENIChomozygous108638044
1266422600266422601AC21GENIChomozygous108638045
1266422930266422931CT20GENIChomozygous108638046
1266423134266423135TC16GENIChomozygous108638047
1266423372266423373TG5GENIChomozygous125327551
1266423463266423464CT15GENIChomozygous108638048
1266424165266424166CT15GENIChomozygous108638049
1266424638266424639GC19GENIChomozygous108638050
1266424690266424691GA24GENIChomozygous108638051
1266425164266425165TG27GENIChomozygous108638052
1266425367266425368AG18GENIChomozygous108638053
1266425809266425810CA18GENIChomozygous108638054
1266425994266425995TC10GENIChomozygous108638055
1266426008266426009CT11GENIChomozygous108638056
1266426009266426010GT12GENIChomozygous108638057
1266426479266426480AG11GENIChomozygous108638058
1266426538266426539GA5GENIChomozygous108638059
1266426608266426609GT5GENIChomozygous108638060
1266428301266428302AG17GENIChomozygous108638061
1266428493266428494TC20GENIChomozygous108638062
1266429181266429182CT17GENIChomozygous108638063
1266429422266429423GA10GENIChomozygous108638064
1266429453266429454GA10GENIChomozygous108638065
1266427600266427600GTATCACAGAGG26GENIChomozygous127509137
1266429585266429586A10GENIChomozygous127509138
1266429822266429823TC13GENIChomozygous108638066
1266429923266429924TC14GENIChomozygous108638067