chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105501385155013852GA3GENIChomozygous116602024
105501484455014845AG25GENIChomozygous117130658
105501491455014915CA18GENIChomozygous116602033
105501663355016634AG9GENIChomozygous116602047
105501666955016670GT15GENIChomozygous116602051
105501930555019306AG21GENIChomozygous117130659
105502087255020873AG17GENIChomozygous116602057
105502221855022219CT16GENIChomozygous117130660
105502227155022272CT20GENIChomozygous117130661
105502273255022733AG13GENIChomozygous117151073
105502360055023601AG14GENIChomozygous117011397
105502415155024152GA16GENIChomozygous117130662
105502541455025415AT23GENIChomozygous116781613
105502541655025417GT25GENIChomozygous116781615
105502555355025554GT22GENIChomozygous116602061
105502581155025812TA25GENIChomozygous116602063
105502650355026504TG32GENIChomozygous117151074
105502935455029355CA18GENIChomozygous117130663
105503028655030287CG12GENIChomozygous116602075
105503066555030666AG18GENIChomozygous116602077
105503192355031924GT20GENIChomozygous116602079
105503720055037201GT20GENIChomozygous117312623
105504514955045150GT3GENIChomozygous116781695
105504515155045152CT3GENIChomozygous116781697
105504915455049155GA22GENIChomozygous116602083
105507312155073122CT7GENIChomozygous116602087