chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151175138151175139GC22GENICpossibly homozygous114155876
5151179599151179600AC10GENIChomozygous114056583
5151181666151181667AG26GENIChomozygous114056585
5151181671151181672GA23GENIChomozygous114056587
5151181676151181677GT20GENIChomozygous114056589
5151181677151181678GT20GENIChomozygous114056591
5151181737151181738AC32GENIChomozygous114056593
5151181738151181739AT34GENIChomozygous114056595
5151181770151181771CG34GENIChomozygous114056597
5151181784151181785TC26GENIChomozygous114056599
5151181798151181799CG16GENIChomozygous114155877
5151181801151181802TA16GENIChomozygous114056601
5151181822151181823TA2GENIChomozygous114155878
5151184962151184963TG23GENICheterozygous114056605
5151185082151185083TG25GENICpossibly homozygous114056607
5151185116151185117AT21GENICheterozygous114056609
5151185229151185230CG41GENICheterozygous114056610
5151188332151188333TC35GENIChomozygous114056612