chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71306282813062829TC38GENIChomozygous115570867
71306285513062856CT40GENICpossibly homozygous115570868
71306400213064003CA14GENICpossibly homozygous115570869
71306647713066478CT39GENICheterozygous115570870
71306648313066484CT36GENICheterozygous115570871
71306648913066490CT34GENICheterozygous115570872
71306650113066502CT31GENICheterozygous115570873
71306650713066508CT35GENICheterozygous115570874
71306742113067422AG49GENIChomozygous115570875
71306754713067548AG44GENIChomozygous115570876
71306785813067859GA51GENIChomozygous115570877
71306856613068567GC37GENICheterozygous115570878
71306902613069027TC41GENIChomozygous115570879
71306984413069845GA42GENIChomozygous115570880