chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3129869693129869694GA28GENIChomozygous111711123
3129869933129869934CT37GENIChomozygous111711125
3129870554129870555AT23GENICheterozygous112028958
3129872251129872252GC24GENIChomozygous111711127
3129875325129875326CA20GENIChomozygous111711129
3129875330129875331GC20GENIChomozygous111711131
3129875335129875336TG21GENIChomozygous111711133
3129875347129875348GA20GENIChomozygous111711135
3129876121129876122TG33GENIChomozygous111711137
3129876441129876442TC41GENIChomozygous111711139
3129877026129877027GC31GENIChomozygous111711141
3129878854129878855AC23GENIChomozygous111711143
3129880825129880826CT19GENIChomozygous111711145
3129880826129880827AG19GENIChomozygous111711147
3129880890129880891GC22GENIChomozygous111711149
3129880988129880989TC21GENIChomozygous111711151
3129881063129881064TC25GENIChomozygous111711153
3129881133129881134GA20GENIChomozygous111711155
3129881397129881398CG23GENIChomozygous111711157
3129881454129881455GT30GENIChomozygous111711159
3129881718129881719CT19GENIChomozygous111711161
3129883731129883732CT27GENIChomozygous111711163
3129883782129883783AC31GENIChomozygous111711165
3129883787129883788TC31GENIChomozygous111711167
3129884006129884007GA34GENIChomozygous111711169
3129884921129884922TC13GENIChomozygous111711171