chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165336498165336499GC13GENIChomozygous108353388
1165337111165337112GA28GENIChomozygous109341338
1165338243165338244GC16GENIChomozygous109341340
1165338556165338557TA25GENIChomozygous108353390
1165343111165343112AG18GENIChomozygous109341342
1165346584165346585CT25GENIChomozygous109341350
1165350245165350246TC17GENIChomozygous108353398
1165351425165351426GA11GENIChomozygous109341352
1165352789165352790TC28GENIChomozygous108353400
1165353401165353402CT11GENIChomozygous109341354
1165354628165354629CA24GENIChomozygous109341356
1165355463165355464GA18GENIChomozygous109341358
1165355603165355604TC27GENIChomozygous109435983
1165356573165356574GA7GENIChomozygous109341360
1165356682165356683CT12GENIChomozygous109341362
1165357092165357093CT5GENIChomozygous109341364
1165357683165357684AC8GENIChomozygous109435985
1165357748165357749GC11GENIChomozygous108353412
1165358933165358934GT21GENIChomozygous109341368
1165361703165361704GT6GENIChomozygous108353420
1165362952165362953GA31GENIChomozygous109341372
1165364082165364083GA17GENIChomozygous109435987
1165367037165367038TG21GENIChomozygous109435991
1165367312165367313AG21GENIChomozygous108353426
1165371885165371886AG8GENIChomozygous109435993
1165376331165376332CT23GENIChomozygous109435995
1165379471165379472TC9GENIChomozygous108353442