chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108993045389930454GC12GENIChomozygous116903701
108993693789936938AT16GENIChomozygous116950862
108993707389937074CG5GENIChomozygous116903705
108994091589940916AG13GENIChomozygous116903707
108994097789940978CT18GENIChomozygous116903709
108995150389951504CT15GENIChomozygous116903711
108995210189952102AG16GENICheterozygous116903713
108995299489952995GA15GENIChomozygous116903715
108995304589953046AG6GENIChomozygous116903717
108995338789953388CT20GENIChomozygous116903719
108995373689953737TC17GENIChomozygous116903721
108995507489955075TC13GENIChomozygous116903723
108995754689957547GC20GENICheterozygous117392083
108993978989939790AG6GENIChomozygous117020523
108993985189939852TG3GENICheterozygous126476330