chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140845519140845520GA27GENIChomozygous962915132
1140846341140846342CT27GENIChomozygous962915133
1140847133140847134AC33GENIChomozygous962915134
1140847185140847186GA35GENIChomozygous962915135
1140847446140847447GA33GENIChomozygous962915136
1140847676140847677CT31GENIChomozygous962915137
1140848394140848395CT18GENIChomozygous962915138
1140848827140848828CT29GENIChomozygous962915139
1140849120140849121CA13GENIChomozygous962915140
1140849499140849500GA32GENIChomozygous962915141
1140850550140850551GT36GENIChomozygous962915142
1140850659140850660GA41GENIChomozygous962915143
1140851129140851130CT10GENIChomozygous962915144
1140851141140851142AT12GENIChomozygous962915145
1140855002140855003AG17GENIChomozygous962915146
1140855711140855712CT32GENIChomozygous962915147
1140857565140857566TC30GENIChomozygous962915148
1140858263140858264GC26GENICpossibly homozygous962915149
1140858312140858313AC34GENIChomozygous962915150