chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133995821133995822GA44GENIChomozygous56932771
4133996100133996101TG33GENIChomozygous56932773
4133996108133996109CT38GENICheterozygous56932774
4133996130133996132TC--24GENICheterozygous56932776
4133996481133996482TG64GENIChomozygous56932778
4133996633133996634GA27GENICpossibly homozygous56932781
4133997886133997887AT51GENIChomozygous56932784
4133997990133997991GA52GENIChomozygous56932785
4133998964133998965CT30GENIChomozygous56932787
4133999373133999374AG31GENICheterozygous57937896
4133996133133996134CT33GENICheterozygous57334148
4133996146133996147TC32GENICheterozygous57836482
4133996154133996155TC32GENICheterozygous57937881
4133997577133997578GA62GENIChomozygous57937884
4133997595133997596GC64GENIChomozygous57937886
4133998672133998673TC40GENIChomozygous57937888
4133998784133998785GA40GENIChomozygous57937890
4133999369133999370TTCATGTCTGATA25GENIChomozygous57937892
4133999372133999373CT32GENICheterozygous57937894