chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162134369621343697AG29GENIChomozygous796024232
162134379121343792TC33GENICpossibly homozygous796024233
162134390921343910GA35GENIChomozygous796024234
162134426721344268AG26GENIChomozygous796024235
162134444021344441CA22GENIChomozygous796024236
162134498621344987GC22GENIChomozygous796024237
162134514821345149CT34GENIChomozygous796024238
162134541621345417AG14GENIChomozygous796024239
162134730921347310TC42GENIChomozygous796024240
162134733721347338AT36GENICpossibly homozygous796024241
162134808621348087AG31GENIChomozygous796024242
162134889221348893CA16GENICpossibly homozygous796024243