chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3165713655165713656CG16GENIChomozygous952073142
3165716419165716420GA29GENIChomozygous952073143
3165716460165716461AG22GENIChomozygous952073144
3165716510165716511GT19GENIChomozygous952073145
3165716853165716854AG23GENIChomozygous952073146
3165717505165717506GA12GENIChomozygous952073147
3165718421165718422AT21GENIChomozygous952073148
3165718770165718771TC26GENIChomozygous952073149
3165719864165719865CT27GENIChomozygous952073150
3165720755165720756TC40GENIChomozygous952073151
3165721423165721424GA13GENIChomozygous952073152
3165723500165723501AG20GENIChomozygous952073153
3165724937165724938CG10GENIChomozygous952073154
3165725110165725111AG26GENIChomozygous952073155
3165725666165725667CG21GENIChomozygous952073156
3165725787165725788GA28GENIChomozygous952073157
3165729494165729495AG10GENIChomozygous952073158
3165730403165730404GA10GENIChomozygous952073159
3165730805165730806CT15GENIChomozygous952073160
3165732815165732816TC23GENIChomozygous952073161
3165733239165733240AG26GENIChomozygous952073162
3165733902165733903AG22GENIChomozygous952073163
3165734051165734052CT41GENIChomozygous952073164
3165734529165734530GA25GENIChomozygous952073165
3165734668165734669AG32GENIChomozygous952073166
3165734746165734747AG23GENIChomozygous952073167
3165734887165734888GA20GENIChomozygous952073168
3165735012165735013CG27GENIChomozygous952073169
3165736652165736653GA28GENIChomozygous952073170
3165738866165738867TC21GENICpossibly homozygous952073171
3165740269165740270CT11GENIChomozygous952073172
3165740601165740602CT23GENIChomozygous952073173
3165740912165740913GA18GENIChomozygous952073174
3165741893165741894GA15GENIChomozygous952073175