chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
711297501129751CA16GENIChomozygous115533077
711366531136654AT36GENIChomozygous115533078
711375961137597CG26GENIChomozygous115533079
711394841139485GA28GENICpossibly homozygous115533080
711395501139551GA14GENIChomozygous115533081
711398531139854GA27GENIChomozygous115533082
711441811144182TA28GENIChomozygous115533083
711461381146139CT19GENIChomozygous115533084
711462951146296GC29GENICheterozygous115533085
711580951158096AT30GENIChomozygous115533086
711736421173643AG28GENIChomozygous115533087
711761771176178CA51GENIChomozygous115533088
711773531177354CG7GENIChomozygous115533089
711780411178042GA18GENIChomozygous115533090
711797711179772CG29GENIChomozygous115533091
711797861179787GT45GENIChomozygous115533092
711799031179904TG28GENIChomozygous115533093
711879791187980GC23GENIChomozygous115533094