chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266422220266422221GA16GENIChomozygous108638044
1266422600266422601AC17GENICpossibly homozygous108638045
1266422930266422931CT19GENIChomozygous108638046
1266423134266423135TC31GENIChomozygous108638047
1266423372266423373TG5GENIChomozygous125327551
1266423463266423464CT22GENIChomozygous108638048
1266424165266424166CT22GENIChomozygous108638049
1266424638266424639GC19GENIChomozygous108638050
1266424690266424691GA24GENIChomozygous108638051
1266425164266425165TG18GENIChomozygous108638052
1266425367266425368AG20GENIChomozygous108638053
1266425809266425810CA25GENIChomozygous108638054
1266425994266425995TC15GENIChomozygous108638055
1266426008266426009CT13GENIChomozygous108638056
1266426009266426010GT13GENIChomozygous108638057
1266426479266426480AG16GENIChomozygous108638058
1266426538266426539GA10GENIChomozygous108638059
1266426608266426609GT7GENICheterozygous108638060
1266428301266428302AG18GENIChomozygous108638061
1266428493266428494TC27GENIChomozygous108638062
1266429181266429182CT18GENIChomozygous108638063
1266429422266429423GA19GENIChomozygous108638064
1266429453266429454GA21GENIChomozygous108638065
1266429822266429823TC18GENIChomozygous108638066
1266429923266429924TC30GENIChomozygous108638067
1266429585266429586A12GENIChomozygous127509138
1266427600266427600GTATCACAGAGG24GENIChomozygous127509137