chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124792412447924125CT13GENIChomozygous115345054
124792455347924554AG21GENIChomozygous115345056
124792455447924555GA21GENIChomozygous115345058
124792506847925069AG10GENIChomozygous115345062
124792694047926941AC10GENIChomozygous115345064
124792697647926977TC10GENIChomozygous115345066
124792766647927667AG17GENIChomozygous115345068
124792773047927731GA17GENIChomozygous115345070
124792773147927732AG17GENIChomozygous115345072
124792779047927791AG10GENIChomozygous115345074
124792811747928118TC13GENIChomozygous115345076
124793041747930418AG8GENIChomozygous115345078
124793156447931565AG13GENIChomozygous115345080
124793281247932813AG10GENIChomozygous115398653