chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2093355409335541T-4GENIChomozygous45423050
2093379439337944AC47GENIChomozygous45423052
2093385849338585GA34GENICpossibly homozygous45423054
2093392719339279CCTGTGGC--------16GENIChomozygous45423056
2093397809339781CA44GENICpossibly homozygous45423058
2093401309340131CT26GENIChomozygous45423060
2093402519340252TTCA12GENIChomozygous45423062
2093404069340407GA37GENIChomozygous45423064
2093410739341077GTGT----13GENIChomozygous45423066
2093410909341091T-22GENICheterozygous45423068
2093410929341097TGGTT-----27GENICheterozygous45423070
2093410959341097TT--21GENICheterozygous45423072
2093411159341118CTC---21GENIChomozygous45423074
2093421159342116CT42GENICpossibly homozygous45423076
2093423279342328C-22GENIChomozygous45423078
2093424859342486A-44GENIChomozygous45423080