chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
49753140897531409GA45GENICpossibly homozygous112790102
49753214197532142GT78GENIChomozygous112790104
49753230397532304GT67GENIChomozygous112790106
49753240697532407TC61GENIChomozygous112790108
49753328397533284TA70GENICpossibly homozygous112790110
49753353497533535CT8GENIChomozygous113044018
49753361097533611GT35GENICpossibly homozygous112790112
49753369797533698CG59GENIChomozygous112790114
49753475097534751TC82GENIChomozygous112790116
49753506697535067AG55GENIChomozygous112790118
49753522997535230AG59GENIChomozygous112790120
49753616397536164GA78GENIChomozygous112790122
49753699797536998AG78GENICpossibly homozygous112790124
49753771697537717GT85GENIChomozygous112790126
49753866697538667TC56GENIChomozygous112790128
49753938497539385GT47GENICpossibly homozygous112790130
49753980097539801GA55GENICpossibly homozygous112790132
49754090897540909TC80GENIChomozygous112790134