chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45767410057674101AG18GENIChomozygous56908837
45767440557674406AG17GENIChomozygous58335415
45767440657674407TA17GENIChomozygous58335416
45767451157674513TT--9GENIChomozygous57730739
45767486857674869CT20GENIChomozygous57730741
45767527757675278GC25GENIChomozygous57730743
45767577457675775CT29GENIChomozygous57730745
45767589357675894TC20GENIChomozygous57730747
45767597657675977TA19GENIChomozygous57730749
45767602557676045CTCTCTCTCTCTCTCTCTCC--------------------4GENICheterozygous58335418
45767655057676551GA25GENIChomozygous57730753
45767655857676559GC23GENIChomozygous57730755
45767663857676639GA23GENIChomozygous57730757
45767682657676827AG20GENIChomozygous57730759
45767722957677239TGTGTGTGTG----------9GENICpossibly homozygous58670574
45767766557677666TTA21GENIChomozygous57834969
45767773057677731GA26GENIChomozygous57730765
45767817157678172CT27GENIChomozygous57730767
45767820957678210G-22GENIChomozygous57834970
45768000057680001CT20GENIChomozygous57730771
45768019757680198AG25GENIChomozygous56908839
45768050257680503TA18GENIChomozygous57730773
45768113457681135TTACACACACACACACACAC4GENICheterozygous58335420
45768113457681135TTACACACACAC4GENICheterozygous58964110
45768149157681492AG20GENIChomozygous57730775
45768194957681950T-19GENIChomozygous57730785
45768195257681960TCCTCCCC--------26GENICpossibly homozygous57730789
45768196957681970CT28GENICpossibly homozygous57730791
45768197557681976AT25GENIChomozygous57730793
45768319457683195CCA11GENICheterozygous57834973
45768319957683200CA15GENIChomozygous57730797
45768406457684065CG27GENIChomozygous57730801
45768464557684646CT31GENIChomozygous56908842
45768479157684792AG25GENIChomozygous56908843
45768533757685338GC42GENIChomozygous57730803
45768569057685691CT30GENIChomozygous56908844
45768575057685751TC26GENIChomozygous56908845
45768575557685756TC26GENIChomozygous56908846
45768583057685831TC20GENIChomozygous57322122
45768583157685832AT20GENIChomozygous56908847