chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761598617615987TC33GENIChomozygous791150114
141761702817617029CA8GENIChomozygous791150115
141762106317621064TC15GENIChomozygous791150116
141762138217621383TC19GENIChomozygous791150117
141762256517622566TA15GENIChomozygous791150118
141762303117623032CT15GENIChomozygous791150119
141762436417624365CT24GENIChomozygous791150120
141762439017624391TC24GENIChomozygous791150121
141762442617624427CG17GENICpossibly homozygous791150122
141762588517625886AG10GENIChomozygous791150123
141762981017629811AG20GENIChomozygous791150124
141762983717629838TC16GENICpossibly homozygous791150125
141762984117629842TC17GENIChomozygous791150126
141762992517629926AG18GENIChomozygous791150127
141763052217630523TA9GENIChomozygous791150128
141763065017630651TG4GENIChomozygous791150129