chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3129869693129869694GA15GENIChomozygous111711123
3129869933129869934CT27GENIChomozygous111711125
3129872251129872252GC24GENIChomozygous111711127
3129875325129875326CA13GENIChomozygous111711129
3129875347129875348GA10GENIChomozygous111711135
3129876121129876122TG17GENIChomozygous111711137
3129876441129876442TC32GENIChomozygous111711139
3129877026129877027GC15GENIChomozygous111711141
3129878854129878855AC56GENIChomozygous111711143
3129878856129878857TA55GENIChomozygous112429854
3129878857129878858AC55GENIChomozygous112429855
3129880825129880826CT17GENIChomozygous111711145
3129880826129880827AG17GENIChomozygous111711147
3129880890129880891GC13GENIChomozygous111711149
3129880988129880989TC24GENIChomozygous111711151
3129881063129881064TC28GENIChomozygous111711153
3129881133129881134GA10GENIChomozygous111711155
3129881397129881398CG25GENIChomozygous111711157
3129881454129881455GT22GENIChomozygous111711159
3129881718129881719CT34GENIChomozygous111711161
3129883731129883732CT44GENIChomozygous111711163
3129883782129883783AC37GENIChomozygous111711165
3129883787129883788TC36GENIChomozygous111711167
3129884006129884007GA31GENIChomozygous111711169
3129884921129884922TC53GENIChomozygous111711171