chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151181666151181667AG27GENIChomozygous114056585
5151181671151181672GA24GENIChomozygous114056587
5151181676151181677GT19GENIChomozygous114056589
5151181677151181678GT20GENIChomozygous114056591
5151181737151181738AC28GENIChomozygous114056593
5151181738151181739AT29GENIChomozygous114056595
5151181770151181771CG21GENIChomozygous114056597
5151181784151181785TC18GENIChomozygous114056599
5151181801151181802TA6GENIChomozygous114056601
5151184961151184962CG44GENICpossibly homozygous114056603
5151184962151184963TG45GENICheterozygous114056605
5151185082151185083TG32GENICpossibly homozygous114056607
5151185229151185230CG49GENICpossibly homozygous114056610
5151188332151188333TC20GENIChomozygous114056612
5151185028151185029AT41GENICheterozygous114451261