chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
49590710795907108GA68GENIChomozygous137124169
49590763595907638AGA36GENIChomozygous136899832
49590784095907841GT55GENIChomozygous137124170
49590800295908003GT47GENIChomozygous137124171
49590810595908106TC51GENIChomozygous137124172
49590898295908983TA47GENIChomozygous137124173
49590939695909397CG30GENICpossibly homozygous137124174
49591044995910450TC45GENIChomozygous137124175
49591076595910766AG38GENIChomozygous137124176
49591092895910929AG42GENIChomozygous137124177
49591186295911863GA43GENIChomozygous137124178
49591222295912223A43GENIChomozygous136899833
49591384995913850G35GENIChomozygous136899834
49591660795916608TC48GENIChomozygous137124183
49591269695912697AG61GENIChomozygous137124179
49591341595913416GT46GENIChomozygous137124180
49591436595914366TC48GENIChomozygous137124181
49591549995915500GA49GENIChomozygous137124182
49591788095917881T41GENIChomozygous136899835