chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245478671245478672CT16GENIChomozygous108599039
1245480598245480599AT8GENIChomozygous108599041
1245480625245480626CT7GENIChomozygous108599043
1245482925245482926TG20GENIChomozygous108599045
1245484706245484707AG19GENIChomozygous108599046
1245484741245484742AC21GENIChomozygous108599048
1245487389245487390TC10GENIChomozygous108599052
1245487458245487459GA20GENIChomozygous108599054
1245489679245489680GT14GENIChomozygous108599056
1245492766245492767TC15GENIChomozygous125321968
1245492963245492964CG4GENIChomozygous125410306
1245493434245493435CA5GENICheterozygous125493109
1245500482245500483AG12GENIChomozygous108599088
1245501182245501183TA16GENICheterozygous108599090
1245501635245501636AT20GENIChomozygous108599092
1245501692245501693CT20GENIChomozygous120601558
1245503750245503751GA13GENIChomozygous108599096
1245504010245504011GA12GENIChomozygous125321969
1245507013245507014TC8GENIChomozygous108599100
1245508345245508346TC11GENIChomozygous108599102
1245508617245508618GA24GENIChomozygous108599104
1245509471245509472GA3GENICheterozygous125493110
1245509605245509606GA17GENIChomozygous108599106
1245509875245509876CT5GENIChomozygous108599108
1245510582245510583CT16GENIChomozygous108599110
1245514258245514259TC18GENIChomozygous108599114
1245515748245515749AG18GENIChomozygous108599116
1245516179245516180AG29GENIChomozygous108599118