chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109016585290165853TTC13GENICheterozygous51537795
109016586190165862TTTG13GENIChomozygous51537796
109016644790166448AAT10GENICheterozygous51537797
109016739590167396GA40GENIChomozygous51736004
109016797990167980CT39GENIChomozygous51537798
109016857790168578TC22GENIChomozygous51537799
109017161090171611CA29GENIChomozygous51537800