chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4189300693189300694CA37GENIChomozygous57027559
4189300695189300696CA34GENIChomozygous57027560
4189300697189300698AACAT33GENIChomozygous58361065
4189300699189300700GT34GENIChomozygous58361067
4189300701189300702GC34GENIChomozygous58361069
4189300703189300705GG--35GENIChomozygous58361071
4189300736189300737TA30GENIChomozygous58361073
4189300737189300738TC28GENIChomozygous58361075
4189300741189300742GC28GENIChomozygous58361077
4189300743189300744GT28GENIChomozygous58361079
4189324634189324636GT--7GENICheterozygous58484672
4189335337189335339AC--15GENICheterozygous58446492
4189343672189343673T-4GENICheterozygous58361081
4189351830189351831AATG3GENICheterozygous58568380
4189354214189354215TC17GENIChomozygous57354526
4189381121189381123GT--5GENICheterozygous58361087
4189343671189343672CCT4GENICheterozygous57566383