chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118450611484506115TC15GENIChomozygous116069914
118450633484506335GA14GENIChomozygous116069916
118450664584506646GA21GENIChomozygous116069918
118450680784506808TC15GENIChomozygous116069920
118450736984507370CT13GENIChomozygous116069922
118450899884508999CT16GENIChomozygous116069926
118450934984509350CT15GENIChomozygous116069928
118451041184510412CT15GENIChomozygous116069930
118451063084510631AG14GENIChomozygous116069932
118451063184510632TC14GENIChomozygous116069934
118451078484510785TC19GENIChomozygous116069936
118451112184511122AG17GENIChomozygous116069938
118451114984511150CG16GENIChomozygous116069940
118451120084511201CT26GENIChomozygous116069942
118451156984511570TC22GENIChomozygous116069944
118451187084511871CT16GENIChomozygous116069946
118451188784511888AG16GENIChomozygous116069948
118451194984511950AG18GENIChomozygous116069950
118451227084512271TC14GENIChomozygous116069952
118451249784512498GA24GENIChomozygous116069954
118451301084513011AG12GENIChomozygous116069956
118451321884513219TG15GENIChomozygous116069958
118451343584513436TC24GENIChomozygous116069960
118451376684513767TA28GENIChomozygous116069962
118451393584513936AG12GENIChomozygous116069964
118451415684514157TC14GENIChomozygous116069966