chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85959424659594247TC5GENIChomozygous116512670
85959452159594522CT13GENIChomozygous116966800
85959513359595134AG19GENIChomozygous116966802
85959521859595219TC20GENIChomozygous116966803
85959563859595639CA27GENIChomozygous116966806
85959578159595782TA14GENIChomozygous116512672
85959592059595921CT11GENIChomozygous118146132
85959611759596118TC6GENIChomozygous126710797
85959627259596273AC10GENIChomozygous116966810
85959632359596324TC7GENIChomozygous116966811
85959633959596340TC8GENIChomozygous116966812
85959778359597784TC8GENIChomozygous118146134
85959846759598468TC19GENIChomozygous116966817
85959887059598871TA12GENIChomozygous118175943
85959968159599682TA6GENICheterozygous116512678
85959985859599859CT14GENIChomozygous118175945
85960001559600016GA16GENIChomozygous117108299
85960039259600393CT19GENIChomozygous118146136
85960097759600978CT10GENIChomozygous118146138
85960234659602347CT19GENIChomozygous118146140
85960271159602712CT25GENIChomozygous118146142
85960303459603035AC6GENIChomozygous116966822
85960305459603055TC5GENIChomozygous116966823
85960319859603199AC10GENIChomozygous116966824
85960322659603227GA16GENIChomozygous118146144
85960338559603386CT15GENIChomozygous118146146
85960343259603433AT11GENIChomozygous118146148
85960355659603557AC6GENIChomozygous126710798
85960356859603569AC8GENIChomozygous126667946
85960359359603594AC6GENIChomozygous126667947
85960359659603597AG9GENIChomozygous118146150
85960361859603619GC13GENIChomozygous126667948
85960375659603757CT16GENIChomozygous116966826
85960378859603789GA23GENIChomozygous116966827
85960384159603842GA4GENIChomozygous116966829
85960441159604412AG12GENIChomozygous116966832
85960553259605533CT20GENIChomozygous116966835
85960609559606096TC20GENIChomozygous116966836