chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10111309564111309565GGT55GENICheterozygous743108118
10111309751111309753AA--16GENIChomozygous743108119
10111310354111310355TTAC1GENIChomozygous743108120
10111311193111311194CCT10GENICheterozygous743108122
10111311194111311195T-10GENICheterozygous743108121
10111311682111311683GGGGTTTTTTTTTGTTT15GENICheterozygous743108124
10111319624111319626AT--25GENICheterozygous743108125
10111319715111319716CCT14GENICheterozygous743108126
10111319811111319812GGTA11GENICpossibly homozygous743108128
10111319866111319868TG--14GENICheterozygous743108130
10111319890111319894TGTC----18GENICheterozygous743108131
10111320438111320439GGAAC22GENICheterozygous743108132
10111321704111321705TTCTC36GENICheterozygous743108133