chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133995821133995822GA11GENIChomozygous56932771
4133996100133996101TG5GENIChomozygous56932773
4133996481133996482TG6GENIChomozygous56932778
4133996633133996634GA5GENIChomozygous56932781
4133997577133997578GA11GENIChomozygous57937884
4133997595133997596GC10GENIChomozygous57937886
4133997886133997887AT14GENICpossibly homozygous56932784
4133997990133997991GA22GENIChomozygous56932785
4133998672133998673TC5GENIChomozygous57937888
4133998784133998785GA12GENICpossibly homozygous57937890
4133998964133998965CT6GENIChomozygous56932787
4133999369133999370TTCATGTCTGATA3GENIChomozygous57937892