chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187772326187772327TC6GENICheterozygous110167779
2187772755187772756AG12GENIChomozygous110167780
2187772910187772911AG11GENIChomozygous110167781
2187772917187772918AG10GENIChomozygous110167782
2187772981187772982TC9GENIChomozygous110167783
2187772999187773000CT12GENIChomozygous111278431
2187773269187773270TA10GENIChomozygous110167784
2187773669187773670CT8GENIChomozygous110167785
2187773716187773717CT10GENIChomozygous110167786
2187773766187773767GC12GENIChomozygous110167787
2187775028187775029TC6GENIChomozygous110167791
2187775157187775158GA8GENIChomozygous110167792
2187775298187775299GC7GENIChomozygous110167793
2187775351187775352AG10GENIChomozygous110167794
2187775385187775386GT9GENIChomozygous110167795
2187775710187775711AG13GENIChomozygous110167796
2187775711187775712TC13GENIChomozygous110167797
2187775820187775821AG7GENIChomozygous110167798
2187776318187776319GC11GENIChomozygous111278433
2187776427187776428CA9GENIChomozygous110804006
2187776519187776520AG9GENIChomozygous110167799
2187776791187776792CT7GENICpossibly homozygous111278437
2187776903187776904AG17GENIChomozygous110167800
2187777516187777517GC9GENIChomozygous110167801
2187777865187777866CT9GENIChomozygous110167802
2187779985187779986GA11GENIChomozygous111278439
2187780489187780490CG13GENIChomozygous111278441
2187780563187780564TC14GENIChomozygous110804011
2187781199187781200AC10GENIChomozygous110167806
2187781206187781207CT11GENIChomozygous111278443
2187781285187781286CT11GENIChomozygous110804013
2187781716187781717CT8GENIChomozygous111278447
2187782274187782275CT17GENIChomozygous111278449
2187782435187782436GA8GENIChomozygous111278451
2187783339187783340GA10GENIChomozygous110167810
2187784664187784665GC16GENIChomozygous110167811