chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133995821133995822GA51GENICpossibly homozygous56932771
4133996058133996059CA32GENIChomozygous56932772
4133996100133996101TG19GENIChomozygous56932773
4133996108133996109CT25GENICheterozygous56932774
4133996118133996119T-16GENICheterozygous56932775
4133996130133996132TC--16GENICheterozygous56932776
4133996284133996285GA21GENIChomozygous56932777
4133996481133996482TG57GENIChomozygous56932778
4133996546133996552GGGAGA------21GENICpossibly homozygous56932779
4133996558133996559GA33GENICheterozygous56932780
4133996633133996634GA30GENICpossibly homozygous56932781
4133996957133996958GA33GENIChomozygous56932782
4133997408133997409TC31GENIChomozygous56932783
4133997886133997887AT31GENIChomozygous56932784
4133997990133997991GA40GENIChomozygous56932785
4133998583133998584TG11GENIChomozygous56932786
4133998964133998965CT11GENIChomozygous56932787
4133999193133999194CT20GENIChomozygous56932788