chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32313369023133691AG20GENIChomozygous111506035
32313404823134049GA26GENICpossibly homozygous111506036
32313409923134100TC23GENIChomozygous111506037
32313660923136610AG53GENICheterozygous111506038
32313661223136613TC53GENICheterozygous111506039
32313662623136627CA54GENICheterozygous111506040
32313663223136633AG50GENICheterozygous111506041
32313758523137586TC32GENIChomozygous111506042
32313887823138879GA30GENIChomozygous111506043
32313929223139293TC21GENIChomozygous111506044
32314201623142017GA37GENIChomozygous111506045
32314248723142488GA31GENIChomozygous111506046
32314419523144196AC17GENIChomozygous111506047
32314489523144896TA22GENIChomozygous111506048
32314614123146142TC20GENIChomozygous111506049
32314633723146338AG30GENIChomozygous111506050
32314655323146554AG31GENICpossibly homozygous111506051
32314750423147505TC11GENIChomozygous111506052
32314757223147573TG25GENIChomozygous111506053
32314783023147831AG18GENIChomozygous111506054