chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105150948951509490A50GENICheterozygous130392590
105154878251548783AC57GENIChomozygous116594416
105155465751554657G33GENIChomozygous128817098
105156100751561008TC16GENIChomozygous123358740
105156100751561007C16GENIChomozygous128817103
105156101051561015TGTTA15GENIChomozygous128817104
105156101751561017TAGG15GENIChomozygous128817105
105156102051561022AA12GENIChomozygous128817106
105156102651561027GC8GENIChomozygous123358745
105156102851561029TC8GENIChomozygous123358746
105156107051561071GA12GENIChomozygous117078291
105158600451586005CA27GENICpossibly homozygous117994137
105159420751594207C15GENIChomozygous128817118
105159421251594213G17GENIChomozygous128817119
105159446851594469GA26GENIChomozygous116594522
105159448051594480A25GENIChomozygous128817126
105159426051594262GC25GENIChomozygous128817120
105159429551594295A37GENIChomozygous128817121
105159429951594299G38GENIChomozygous128817122
105159437251594372T41GENIChomozygous128817123
105159437951594379T44GENIChomozygous128817124
105159444651594446T28GENIChomozygous128817125
105158892251588922T36GENICheterozygous130681810
105159450751594507T22GENIChomozygous128817127
105159451751594517C24GENIChomozygous128817128
105165635351656353C65GENIChomozygous128817148
105165739651657396C45GENIChomozygous128817149
105165740051657400AC47GENIChomozygous128817150
105165740851657409C43GENIChomozygous128817151
105165752751657528CG38GENIChomozygous116884939
105165753051657530TGT38GENIChomozygous128817152
105165768451657684C16GENIChomozygous129969015