chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105577414855774149CG18GENIChomozygous116602839
105577425155774252AG21GENIChomozygous116602841
105577430955774310GA18GENIChomozygous116934989
105577440855774409AG23GENIChomozygous116602843
105577510155775102AG21GENIChomozygous116602844
105577518055775181GA22GENIChomozygous116602846
105577572055775721TC15GENIChomozygous116602848
105577583155775832CT12GENIChomozygous116602850
105577619155776192CG14GENIChomozygous116602854
105577661155776612GA23GENIChomozygous116602856
105577734455777345AG22GENIChomozygous116602858
105577813155778132CT20GENIChomozygous116934991
105577813555778136GA20GENIChomozygous116602860
105577852155778522AG28GENIChomozygous116602862
105577877855778779CT24GENIChomozygous116602864
105577890255778903GA19GENIChomozygous116602866
105577978755779788AG17GENIChomozygous117195988
105577982055779821GC21GENIChomozygous116602868
105577998055779981GT15GENIChomozygous116602870
105578007255780073TC15GENIChomozygous116602872
105578070655780707TG14GENIChomozygous116602874
105578160055781601TC19GENIChomozygous116782852
105578187255781873TC18GENIChomozygous116602878