chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761639017616391CT12GENIChomozygous945007026
141761847117618472TA38GENIChomozygous945007027
141762138217621383TC37GENIChomozygous945007028
141762256517622566TA29GENIChomozygous945007029
141762436417624365CT24GENIChomozygous945007030
141762439017624391TC21GENIChomozygous945007031
141762588517625886AG34GENIChomozygous945007032
141762709017627091CA28GENIChomozygous945007033
141762915917629160GT31GENIChomozygous945007034
141762980417629805AG37GENIChomozygous945007035
141762981017629811AG35GENIChomozygous945007036
141763140917631410CT36GENIChomozygous945007037