chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7114341675114341679GTGA4GENIChomozygous128508127
7114341688114341691GAG4GENIChomozygous128508128
7114341717114341717GCCCCTCTG4GENIChomozygous128508129
7114341731114341732GT10GENIChomozygous128561838
7114341733114341733CCATGAAATCCTTTTATTATTT10GENIChomozygous128508130
7114341738114341739GC9GENIChomozygous128561839
7114341752114341752TCTCACATTT10GENIChomozygous128508131
7114341754114341754CCC13GENIChomozygous128508132
7114341757114341758GC15GENIChomozygous128561840
7114341758114341759AT15GENIChomozygous128561841
7114341762114341762CT15GENIChomozygous128508133
7114341765114341769GAGG17GENIChomozygous128508134
7114341770114341770CTCACT18GENIChomozygous128508135
7114341775114341775TT18GENIChomozygous128508136
7114341776114341777GC20GENIChomozygous128561842
7114341778114341779GC20GENIChomozygous128561843
7114341780114341781GC20GENIChomozygous128561844
7114341781114341782AT20GENIChomozygous128561845
7114341784114341784ACTCT22GENIChomozygous128508137
7114341785114341786GC23GENIChomozygous128561846
7114341787114341788GC23GENIChomozygous128561847
7114341789114341791GG25GENIChomozygous128508138
7114341794114341795GC25GENIChomozygous128561848
7114341797114341797TCCTCCT25GENIChomozygous128508139
7114341798114341799GC29GENIChomozygous128561849
7114341800114341802GG29GENIChomozygous128508140
7114341803114341804GT30GENIChomozygous128561850
7114341806114341811AGGGA30GENIChomozygous128508141
7114341811114341812AC30GENIChomozygous128561851