chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266257617266257618GA15GENIChomozygous108637750
1266259480266259481TG17GENIChomozygous108637751
1266259955266259956TC12GENIChomozygous108637752
1266260071266260072AC32GENIChomozygous108637753
1266260704266260705GA19GENIChomozygous108637754
1266260846266260847TA6GENIChomozygous108637755
1266261396266261397GC16GENIChomozygous108637756
1266262006266262007GC5GENIChomozygous120477296
1266262051266262052TC8GENIChomozygous108637757
1266262303266262304AG20GENIChomozygous108637758
1266263068266263069CA17GENIChomozygous108637760
1266264337266264338TA18GENIChomozygous108637761
1266264589266264590AG12GENIChomozygous108637762
1266265228266265229AG17GENIChomozygous108637763
1266266712266266713CT19GENIChomozygous108637765
1266267954266267955TC18GENIChomozygous108637766
1266268309266268310GA9GENIChomozygous108637767
1266270325266270326AG6GENIChomozygous108637768
1266268556266268557GC4GENIChomozygous125327541