chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45675752456757525CT49GENIChomozygous112657111
45675793956757940AG53GENIChomozygous112657112
45675910256759103TG41GENIChomozygous112657113
45675955456759555AG42GENIChomozygous112657115
45676024356760244AG23GENIChomozygous112657116
45676333656763337AG38GENIChomozygous112657118
45676596256765963CA47GENIChomozygous112657119
45676676156766762CT45GENIChomozygous112657120
45676750756767508AT32GENIChomozygous112657121
45677015356770154GA26GENIChomozygous112657122
45677051856770519CT41GENIChomozygous112657123
45677323956773240TC32GENIChomozygous112657124
45677661556776616CG47GENIChomozygous112657125
45677665956776660CT53GENIChomozygous112657126
45678290156782902CA40GENIChomozygous112657127
45678398756783988TC39GENIChomozygous112657128
45678402556784026TC45GENIChomozygous112657129
45678443456784435AC20GENIChomozygous112657131
45678504856785049TG54GENICpossibly homozygous112657132
45678528556785286CA37GENIChomozygous112657133
45678542156785422AG61GENIChomozygous112657134
45678571356785714AG30GENIChomozygous112657135
45678572856785729AC30GENIChomozygous112657136
45678614156786142TC30GENIChomozygous112657137
45678703356787034AC24GENIChomozygous112657138
45678711656787117TC32GENIChomozygous112657139
45678732356787324AG22GENIChomozygous112657140
45678745556787456AG32GENIChomozygous112657141
45678929756789298AC40GENIChomozygous112657144
45679292556792926AG44GENIChomozygous112657147
45679409456794095CT30GENIChomozygous112657148
45679435456794355CT55GENIChomozygous112657149
45679466656794667CT35GENIChomozygous112657150
45679519456795195CT35GENIChomozygous112657151
45679534356795344TC47GENIChomozygous112657152
45679548956795490AC55GENIChomozygous112657153
45679553056795531AC43GENIChomozygous112657154
45679560356795604AG49GENIChomozygous112657155
45679561656795617AG45GENIChomozygous112657156
45679624056796241GC46GENIChomozygous112657157
45679630356796304TA47GENIChomozygous112657158
45679651856796519TC34GENIChomozygous112657159