chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108993068689930687TC16GENIChomozygous116903703
108993313689933137GA15GENIChomozygous117279304
108993693789936938AT24GENIChomozygous116950862
108993707389937074CG20GENIChomozygous116903705
108993920289939203TC4GENICheterozygous126435026
108993978989939790AG14GENIChomozygous117020523
108994091589940916AG17GENIChomozygous116903707
108994097789940978CT23GENIChomozygous116903709
108995150389951504CT15GENIChomozygous116903711
108995210189952102AG24GENICpossibly homozygous116903713
108995299489952995GA15GENIChomozygous116903715
108995304589953046AG28GENIChomozygous116903717
108995338789953388CT26GENIChomozygous116903719
108995373689953737TC10GENIChomozygous116903721
108995507489955075TC14GENIChomozygous116903723
108995754689957547GC16GENICheterozygous117392083