chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45767410057674101AG22GENIChomozygous56908837
45767440557674406AG12GENICheterozygous58335415
45767440657674407TA11GENICpossibly homozygous58335416
45767451157674513TT--6GENIChomozygous57730739
45767486857674869CT17GENIChomozygous57730741
45767527757675278GC18GENIChomozygous57730743
45767577457675775CT14GENICpossibly homozygous57730745
45767589357675894TC17GENIChomozygous57730747
45767597657675977TA13GENICpossibly homozygous57730749
45767602557676045CTCTCTCTCTCTCTCTCTCC--------------------6GENICheterozygous58335418
45767655057676551GA31GENIChomozygous57730753
45767655857676559GC33GENIChomozygous57730755
45767663857676639GA38GENIChomozygous57730757
45767682657676827AG16GENIChomozygous57730759
45767723757677239TG--6GENICheterozygous58335419
45767766557677666TTAA15GENIChomozygous57730763
45767773057677731GA28GENIChomozygous57730765
45767817157678172CT31GENIChomozygous57730767
45767893257678933CT24GENIChomozygous59494792
45767950657679507T-16GENICpossibly homozygous57730769
45768000057680001CT21GENIChomozygous57730771
45768019757680198AG14GENIChomozygous56908839
45768050257680503TA19GENIChomozygous57730773
45768113457681135TTACACACACACACACACAC6GENIChomozygous58335420
45768149157681492AG19GENIChomozygous57730775
45768193457681943TCCTCCTCT---------8GENIChomozygous57730777
45768196957681970CT14GENIChomozygous57730791
45768197557681976AT17GENIChomozygous57730793
45768231957682320GA22GENIChomozygous57730795
45768319957683200CA12GENIChomozygous57730797
45768386857683873ATGTT-----16GENIChomozygous57730799
45768406457684065CG24GENIChomozygous57730801
45768464557684646CT26GENIChomozygous56908842
45768479157684792AG29GENIChomozygous56908843
45768533757685338GC30GENIChomozygous57730803
45768569057685691CT31GENICpossibly homozygous56908844
45768575057685751TC29GENICpossibly homozygous56908845
45768575557685756TC28GENICpossibly homozygous56908846
45768583057685831TC35GENICpossibly homozygous57322122
45768583157685832AT35GENICpossibly homozygous56908847