chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2105594284105594285TC21GENIChomozygous125577905
2105594462105594463GT7GENIChomozygous125577906
2105594544105594545TC15GENIChomozygous125577907
2105594625105594626GA15GENIChomozygous125577908
2105594635105594636AG16GENIChomozygous125577909
2105594741105594742CG26GENIChomozygous125577910
2105594782105594783CT26GENIChomozygous125577911
2105595075105595076GT17GENIChomozygous125577912
2105595297105595298CT17GENIChomozygous125577913
2105595382105595383CG31GENIChomozygous125577914
2105595863105595864AG19GENIChomozygous125577915
2105596044105596045GC15GENIChomozygous125577916
2105596208105596209CT16GENIChomozygous125577917
2105596221105596222AT13GENIChomozygous125577918
2105596383105596384TG22GENIChomozygous125577919
2105596676105596677CG18GENIChomozygous125577920
2105596778105596779GA17GENIChomozygous125577921
2105596803105596804AG15GENIChomozygous125577922
2105596829105596830CG16GENIChomozygous125577923
2105601054105601055GC6GENIChomozygous125577924
2105607461105607462GA28GENIChomozygous125577925
2105607580105607581AG8GENIChomozygous125577926
2105608021105608022GT16GENIChomozygous125577927
2105608525105608526AG21GENIChomozygous125577928
2105608535105608536CG22GENIChomozygous125577929
2105608695105608696CT4GENIChomozygous125577930
2105608894105608895TC8GENICheterozygous125577931
2105608996105608997AG6GENIChomozygous125577932
2105609084105609085AG11GENIChomozygous125577933
2105609508105609509GC19GENIChomozygous125577934
2105609562105609563CA10GENICheterozygous125577935
2105609960105609961AG5GENICheterozygous125577936
2105609961105609962AG5GENICheterozygous125577937
2105610010105610011AT24GENIChomozygous125577938
2105610286105610287AC6GENIChomozygous125577939
2105610287105610288CT5GENIChomozygous125577940
2105610398105610399AG16GENICheterozygous125577941
2105611050105611051AC18GENIChomozygous125577942
2105611690105611691CG9GENIChomozygous125577943