chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87622697776226978AAT20GENICpossibly homozygous53127158
87622713976227143TTTT----19GENICheterozygous53127159
87622714176227143TT--19GENICpossibly homozygous53127160
87622738076227381AAGG13GENICheterozygous53127161
87622738376227384CCGT13GENICheterozygous53127162
87622741376227415GG--16GENICpossibly homozygous53127163
87622741776227421CGTA----14GENICpossibly homozygous53127164
87622745876227459GA31GENIChomozygous53127165
87622754976227550GA37GENIChomozygous53127166
87622773076227731AAG35GENIChomozygous53127167
87622799676227997GA31GENICpossibly homozygous53127168
87622978076229781AT22GENICpossibly homozygous53127169
87623020376230204AAG27GENIChomozygous53127170
87623029176230292TA39GENIChomozygous53127171
87623035076230351TC25GENIChomozygous53127172
87623035276230353CA27GENICpossibly homozygous53127173
87623040676230407AAGGGCT15GENIChomozygous53127174
87623096276230963AG11GENIChomozygous53127176
87623105976231060TTG3GENIChomozygous53127177
87623120276231203C-21GENIChomozygous52998387
87623121276231213CT21GENICpossibly homozygous53182508
87623154176231542GA40GENIChomozygous53127178
87623158476231585TC28GENIChomozygous53127179
87623174876231749CT28GENIChomozygous53127180
87623192976231930TC24GENIChomozygous53127181
87623204076232041GGAT7GENIChomozygous53127182
87623207876232079AATACG7GENICheterozygous53127183
87623207976232081TG--7GENICheterozygous53182509
87623212276232126TATA----4GENICheterozygous52677198
87623220076232204TATA----5GENICheterozygous53127184
87623225476232255CT11GENICheterozygous53127185
87623226776232268GGAT7GENIChomozygous53127186
87623230376232309ATATAT------4GENIChomozygous53127187
87623293576232936TC25GENIChomozygous53127188
87623308776233088GC40GENIChomozygous53127189
87623315076233151A-1GENIChomozygous53182510