chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109539468109539469GC35GENIChomozygous116718565
10109539891109539892GT37GENIChomozygous117136817
10109545161109545162GA36GENICpossibly homozygous117136818
10109545432109545433TC29GENICheterozygous118076509
10109547178109547179CT37GENIChomozygous117136819
10109548870109548871TC18GENIChomozygous117297596
10109549499109549500AG39GENIChomozygous116718569
10109549959109549960CG28GENIChomozygous116718571
10109550184109550185TC29GENIChomozygous116718573
10109552366109552367AC33GENIChomozygous116718577