chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161431676114316762AG13GENIChomozygous111732825
161431754714317548TG19GENIChomozygous111732827
161431834514318346AT11GENIChomozygous111732829
161431878014318781GC12GENIChomozygous111732831
161431879714318798CA11GENIChomozygous111732833
161431881114318812GA11GENIChomozygous111732835
161431895714318958CA15GENIChomozygous111732837
161431900814319009CA12GENIChomozygous111732839
161431920514319206CT4GENIChomozygous111732842
161431921614319217GT5GENIChomozygous111732844
161431983614319837GA23GENIChomozygous111732848
161431991014319911AC14GENIChomozygous111732850
161432002514320026GA16GENIChomozygous111732852
161432005314320054TA15GENICheterozygous111732854
161432008414320085TC17GENIChomozygous111732856
161432011514320116AG9GENIChomozygous111732858
161432062814320629CT10GENIChomozygous111732860
161432086114320862GC7GENIChomozygous111732862
161432140814321409TA18GENIChomozygous111732864
161432143814321439CA18GENIChomozygous111732866
161432155214321553AG18GENIChomozygous111732868
161432163914321640AG15GENIChomozygous111732870
161432189014321891AC11GENIChomozygous111732872
161432235514322356AG20GENIChomozygous111732874
161432243914322440GA22GENIChomozygous111732876
161432497114324972TA11GENIChomozygous125649718