chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133995821133995822GA17GENIChomozygous56932771
4133996100133996101TG15GENIChomozygous56932773
4133996118133996119T-4GENIChomozygous56932775
4133996481133996482TG16GENIChomozygous56932778
4133996633133996634GA15GENIChomozygous56932781
4133997886133997887AT21GENIChomozygous56932784
4133997990133997991GA25GENIChomozygous56932785
4133998964133998965CT11GENIChomozygous56932787
4133999369133999370TTCATGTCTGATA33GENICpossibly homozygous57937892
4133996122133996123T-4GENIChomozygous58338299
4133996126133996127TC4GENIChomozygous58338300
4133996132133996134TC--6GENIChomozygous59494857
4133997577133997578GA28GENIChomozygous57937884
4133997595133997596GC30GENIChomozygous57937886
4133998672133998673TC11GENIChomozygous57937888
4133998784133998785GA14GENIChomozygous57937890