chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142093570320935704CT36GENIChomozygous809197151
142093596520935966GA41GENIChomozygous809197152
142093635020936351GA39GENIChomozygous809197153
142093783520937836TG34GENICheterozygous809197154
142093808320938084GA13GENICheterozygous809197155
142093833620938337TG55GENIChomozygous809197156
142093903820939039AT43GENIChomozygous809197157
142093939420939395AG43GENIChomozygous809197158
142094203720942038TG7GENIChomozygous809197159
142094208520942086CA27GENIChomozygous809197160
142094214020942141CG33GENICpossibly homozygous809197161
142094222920942230TC48GENIChomozygous809197162
142094223220942233CA48GENIChomozygous809197163
142094261420942615GC48GENICpossibly homozygous809197164
142094468420944685AG38GENIChomozygous809197165
142094491220944913AG51GENIChomozygous809197166
142094601420946015AT43GENIChomozygous809197167
142094757020947571AG45GENICpossibly homozygous809197168
142094821820948219GA47GENIChomozygous809197169
142094838320948384GA35GENIChomozygous809197170
142094843520948436AT27GENIChomozygous809197171
142094898520948986GC36GENIChomozygous809197172
142094898920948990TA35GENIChomozygous809197173
142094899220948993GT37GENIChomozygous809197174
142094899820948999TA38GENIChomozygous809197175
142094900620949007AT36GENIChomozygous809197176
142094900820949009GC36GENIChomozygous809197177
142094954020949541TG35GENIChomozygous809197178
142094956220949563AT31GENICpossibly homozygous809197179
142095042120950422CA47GENIChomozygous809197180
142095107520951076CT53GENIChomozygous809197181
142095222620952227CT19GENIChomozygous809197182