chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96862716068627161CG12GENIChomozygous120278400
96865325168653252AC18GENIChomozygous117583990
96869883668698837TC15GENICheterozygous120427996
96887142868871429AC5GENICheterozygous120427997
96889903068899031GC17GENIChomozygous117372703
96891225468912255CT36GENIChomozygous117372705
96891369568913696AC5GENIChomozygous117372707
96891374068913741GA12GENIChomozygous117372709
96927727669277277GC10GENICheterozygous120427998
96934004669340047TG3GENIChomozygous117372737
96938003969380040TG17GENIChomozygous117584002
96938118469381185GT14GENIChomozygous117584006
96938119669381197GC13GENIChomozygous117584008
96938119769381198CG13GENIChomozygous117584010
96940999069409991GT34GENIChomozygous117713761
96940999569409996AG34GENIChomozygous117713763
96940999769409998CG35GENIChomozygous117713765
96941000169410002CG35GENIChomozygous117372751
96942010069420101CA8GENICpossibly homozygous117372755