chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124976941124976942CT9GENIChomozygous54514672
7124977294124977295TC20GENIChomozygous54240013
7124980563124980564C-17GENIChomozygous54514674
7124982040124982041GA22GENIChomozygous54514676
7124983242124983243CG4GENIChomozygous54240029
7124985320124985321CCA14GENIChomozygous54095729
7124985482124985483CT8GENIChomozygous54514684
7124986612124986613CA15GENICpossibly homozygous54514686
7124986928124986929TC9GENIChomozygous54240033
7124987082124987083CA2GENICheterozygous55145135
7124987087124987088CA2GENICheterozygous54240037
7124987189124987190TC5GENIChomozygous54240041