chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171056730410567305GC23GENIChomozygous110954352
171056796110567962GA19GENIChomozygous110954354
171056985710569858TC25GENICpossibly homozygous110954356
171057072410570725GA23GENIChomozygous110954358
171057225110572252AG25GENIChomozygous110954360
171057228810572289CG29GENIChomozygous110954362
171057238110572382CT27GENIChomozygous110954364
171057243510572436CT36GENIChomozygous110954366
171057264110572642TC24GENIChomozygous110954368
171057285810572859AT36GENIChomozygous110954370
171057312210573123GT29GENIChomozygous110954372
171057363910573640GA30GENIChomozygous110954374
171057432610574327GA29GENIChomozygous111231018