chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18911331389113314TC16GENICpossibly homozygous120560880
18911336189113362CT8GENIChomozygous120780166
18911351989113520CT22GENIChomozygous120560884
18911378489113785CT22GENIChomozygous120780167
18911397489113975GT19GENIChomozygous120560886
18911509189115092GC28GENIChomozygous109307815
18911567089115671GA17GENIChomozygous120780168
18911578289115783AG13GENIChomozygous120817276
18911590289115903GA21GENIChomozygous120780169
18911593589115936CT26GENIChomozygous120780170
18911608989116090CA26GENIChomozygous120780171
18911621589116216AG26GENIChomozygous120560890
18911651389116514AT27GENIChomozygous120560892
18911697089116971CT26GENIChomozygous109307817
18911702589117026CT14GENIChomozygous120560894
18911710589117106CT22GENIChomozygous120560896
18911745089117451CG19GENIChomozygous120668735
18911765589117656TG32GENIChomozygous120780172
18911767489117675GT30GENIChomozygous120560900
18911852789118528AG38GENIChomozygous120780173
18911897089118971TC20GENIChomozygous120560904
18911935689119357AG28GENIChomozygous120780174
18911995989119960GA22GENIChomozygous120780175
18912032189120322GA26GENIChomozygous120668737
18912098389120984CT30GENIChomozygous120810174
18912108489121085AG29GENIChomozygous120560914
18912116889121169AG21GENIChomozygous120560916
18912174489121745GA24GENIChomozygous120560918
18912191489121915CT28GENIChomozygous120560920
18912344689123447AG25GENIChomozygous120560922
18912388089123881TG13GENIChomozygous120560924
18912388189123882TC13GENIChomozygous120560926
18912398789123988GC24GENIChomozygous120780176
18912434189124342GC16GENIChomozygous120560930
18912476089124761TG15GENIChomozygous108884724
18912478489124785AT18GENIChomozygous120668739
18912495989124960TG16GENIChomozygous120560932