chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264095442264095443AG23GENIChomozygous960076656
1264095886264095887AG26GENIChomozygous960076657
1264097432264097433TC26GENIChomozygous960076658
1264097633264097634AC26GENIChomozygous960076659
1264097682264097683GA21GENIChomozygous960076660
1264099882264099883CT21GENIChomozygous960076661
1264099931264099932CT26GENIChomozygous960076662
1264100059264100060TA19GENIChomozygous960076663
1264100188264100189AG25GENICpossibly homozygous960076664
1264100432264100433GA17GENIChomozygous960076665
1264100637264100638TC31GENIChomozygous960076666
1264100851264100852AG25GENIChomozygous960076667
1264100853264100854AT24GENIChomozygous960076668
1264101725264101726TA21GENIChomozygous960076669
1264101841264101842AG24GENIChomozygous960076670
1264102013264102014GA23GENIChomozygous960076671
1264102022264102023CT23GENIChomozygous960076672
1264102091264102092GA25GENICpossibly homozygous960076673
1264102112264102113TC23GENIChomozygous960076674
1264102373264102374GA34GENIChomozygous960076675
1264102418264102419TC24GENIChomozygous960076676
1264102632264102633CT28GENIChomozygous960076677
1264103104264103105GA7GENIChomozygous960076678
1264103285264103286AG17GENIChomozygous960076679
1264103682264103683CT18GENICpossibly homozygous960076680
1264104414264104415GA28GENIChomozygous960076681
1264105443264105444AC14GENIChomozygous960076682