chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185644010256440103CT12GENIChomozygous142657117
185644038756440388AG25GENIChomozygous142657118
185644205056442051AG17GENIChomozygous142657119
185644368956443690CT16GENIChomozygous142657120
185644373356443734CT15GENIChomozygous142657121
185644544056445441GA22GENIChomozygous142657122
185644598956445990TC17GENIChomozygous142657123
185644787156447872AC16GENIChomozygous142657124
185644804656448047CG21GENIChomozygous142657125
185644814656448147GA22GENIChomozygous142657126
185644829656448297TC24GENIChomozygous142657127
185644921256449213GA12GENIChomozygous142657128
185644955256449553CT23GENIChomozygous142657129
185644967656449677GA28GENIChomozygous142657130
185644991156449912GA22GENIChomozygous142657131
185645042356450424TC17GENIChomozygous142657132
185645084356450844TC23GENIChomozygous142657133
185645152756451528AG13GENIChomozygous142657134
185645177856451779CA22GENIChomozygous142657135
185645186356451864AT22GENIChomozygous142657136
185645232456452335GACTATTCTGA16GENIChomozygous142631742
185645281156452814TAG13GENIChomozygous142631743
185645762156457622GA14GENIChomozygous142657137
185645809056458091TG18GENICpossibly homozygous142657138
185645868156458681T18GENIChomozygous142631744