chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15769337357693374TC6GENIChomozygous108112106
15769706657697067AG5GENIChomozygous108112107
15770039157700392AG6GENIChomozygous108112110
15770730457707305TG8GENICpossibly homozygous108112113
15770745957707460AC5GENIChomozygous108112114
15770891057708911GT6GENIChomozygous108112115
15771332657713327TG10GENIChomozygous108112116
15771335657713357CT11GENIChomozygous108112117
15771358357713584CT14GENIChomozygous108112118
15771818457718185AG3GENIChomozygous108112119
15771909657719097TC7GENIChomozygous108112120
15771954757719548TC1GENIChomozygous109043051
15772548157725482TG4GENIChomozygous108112122
15772548657725487AT5GENIChomozygous108112123
15772918757729188GC16GENIChomozygous108112125
15772925657729257TC15GENIChomozygous108112126
15773004457730045GA9GENIChomozygous108112127
15773284157732842AG9GENIChomozygous108112128
15773353857733539GA5GENIChomozygous108112129
15773374157733742CA5GENIChomozygous108112130
15773426157734262GA5GENIChomozygous108112131
15773838057738381GT4GENIChomozygous108112133
15774047857740479GC15GENIChomozygous108112135
15774065657740657TG10GENIChomozygous108112136
15774347857743479TC8GENIChomozygous108112138
15774667957746680AT7GENIChomozygous120471671
15774682657746827TC6GENIChomozygous108112139
15775114457751145CT4GENIChomozygous108112140
15775331857753319CT10GENIChomozygous108112141
15775520757755208GC11GENIChomozygous108112142
15775548957755490AC13GENIChomozygous108112143
15774636557746366CT2GENIChomozygous120480250