chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7102294939102294940TA27GENIChomozygous116262530
7102295651102295652GT25GENIChomozygous116298736
7102295656102295657AG23GENIChomozygous116298738
7102295683102295684TC27GENICpossibly homozygous116262531
7102296285102296286GA39GENIChomozygous116298740
7102296325102296326GA44GENIChomozygous116298742
7102296530102296531CG32GENIChomozygous116218488
7102297521102297522CT43GENIChomozygous116298744
7102297620102297621AG31GENIChomozygous116066525
7102296637102296638TC39GENIChomozygous116066521
7102297372102297373TC38GENIChomozygous116066523
7102298171102298172AG27GENIChomozygous116066527
7102298310102298311CG28GENIChomozygous116066529