chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98181616581816166TC62GENIChomozygous660794193
98181624681816247G-40GENICpossibly homozygous763503270
98181635781816361TTTT----39GENIChomozygous763503271
98181636081816361TTCGC39GENIChomozygous763503272
98181640181816402G-28GENIChomozygous763503273
98181645881816459CT34GENIChomozygous660794194
98181645981816460CT33GENIChomozygous660794195
98181646081816461CA35GENIChomozygous660794196
98181752481817525TA53GENIChomozygous660794197
98181915381819154TC49GENIChomozygous660794198
98181926781819268GC55GENIChomozygous660794199
98182024281820243T-14GENICheterozygous763503274
98182041681820417CCACACACACACACACACA17GENICheterozygous763503276
98182171081821711TTG14GENICpossibly homozygous763503278
98182226481822265AG40GENIChomozygous660794200
98182253181822541CTCTCTCTCC----------3GENIChomozygous763503279
98182284381822844C-33GENIChomozygous763503281
98182421881824219AG25GENIChomozygous660794201