chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2186872843186872844TC22GENIChomozygous110166730
2186873747186873748CT28GENICpossibly homozygous110166731
2186876262186876263AG21GENIChomozygous110166732
2186876868186876869CA25GENIChomozygous110166734
2186878686186878687GA22GENIChomozygous110166735
2186879750186879751AG25GENIChomozygous110166736
2186882059186882060AG31GENIChomozygous110166737
2186882119186882120TC36GENIChomozygous110166738
2186885039186885040TC37GENIChomozygous110166739
2186885435186885436TC30GENIChomozygous110166740
2186885613186885614GA23GENIChomozygous110166741
2186885877186885878TC13GENIChomozygous110166742
2186885988186885989TC25GENIChomozygous110166743
2186886027186886028AG27GENIChomozygous110166744
2186886039186886040TC25GENIChomozygous110166745
2186886225186886226CT21GENICpossibly homozygous110166746
2186886246186886247CG23GENIChomozygous110166747
2186886253186886254AG24GENIChomozygous110166748