chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4189300693189300694CA27GENIChomozygous57027559
4189300695189300696CA27GENIChomozygous57027560
4189300697189300698AACAT27GENIChomozygous58361065
4189300699189300700GT27GENIChomozygous58361067
4189300701189300702GC27GENIChomozygous58361069
4189300703189300705GG--28GENIChomozygous58361071
4189300736189300737TA20GENIChomozygous58361073
4189300737189300738TC20GENIChomozygous58361075
4189300741189300742GC22GENIChomozygous58361077
4189300743189300744GT22GENIChomozygous58361079
4189340282189340283TTAC9GENICheterozygous58484676
4189342713189342715TG--22GENICheterozygous57996372
4189343671189343672CCT11GENICheterozygous57566383
4189343672189343673T-11GENICheterozygous58361081
4189351830189351831AATG8GENICheterozygous58568380
4189354214189354215TC21GENIChomozygous57354526
4189381121189381123GT--8GENICheterozygous58361087