chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
59033930190339302CT15GENIChomozygous113916057
59033945590339456CT13GENIChomozygous113916058
59033950290339503AG7GENIChomozygous113916059
59033954090339541AG7GENIChomozygous113916060
59033978390339784AT4GENIChomozygous113916061
59034089890340899AC13GENIChomozygous113916062
59034157190341572GT5GENIChomozygous113916064
59034234290342343AC9GENIChomozygous113916065
59034317690343177GA15GENICpossibly homozygous113916066
59034326690343267TC9GENIChomozygous113916067
59034373390343734GT12GENIChomozygous113916068
59034407390344074CA7GENIChomozygous113916069
59034444990344450AG9GENIChomozygous113916070
59034450890344509AG14GENIChomozygous113916071
59034458290344583GT12GENIChomozygous113916072
59034462190344622CG13GENIChomozygous113916073
59034640890346409TA8GENIChomozygous113916074
59034658690346587CT13GENIChomozygous113916075
59034743390347434CT7GENIChomozygous113916076
59034780390347804AC10GENIChomozygous113916077
59034792090347921GA8GENIChomozygous113916078
59034798690347987GA7GENIChomozygous113916079
59034813490348135TC8GENIChomozygous113916080
59034850390348504CT7GENIChomozygous113916082
59034985690349857GT9GENIChomozygous113916083
59034992490349925TC8GENIChomozygous113916084
59035057290350573AG12GENIChomozygous113916085
59035065290350653GA8GENIChomozygous113916086
59035090290350903GA9GENIChomozygous113916087
59035097290350973TG5GENIChomozygous113916088
59035130390351304TC7GENIChomozygous113916089
59035139390351394AG9GENIChomozygous113916090
59035142990351430AC11GENIChomozygous113916091
59035177390351774GA12GENIChomozygous113916092
59035190890351909AG7GENIChomozygous113916093
59035204190352042TC13GENIChomozygous113916094
59035262890352629TA8GENIChomozygous113916095
59035267490352675TA9GENIChomozygous113916096
59035291990352920CT4GENIChomozygous113916097