chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5154311076154311076AATAACCCC61GENIChomozygous128260283
5154311085154311085A62GENIChomozygous128260284
5154311243154311243C49GENIChomozygous128260285
5154311245154311245GCTC50GENIChomozygous128260286
5154311472154311473AG40GENIChomozygous114060736
5154311831154311832TA44GENIChomozygous114060738
5154312525154312526AG35GENICheterozygous131863103
5154312526154312527AG35GENICpossibly homozygous128302158
5154312528154312529AG34GENICheterozygous131863104
5154312529154312530AG33GENICpossibly homozygous128302159
5154312814154312815CT56GENIChomozygous114060740
5154313882154313883CT45GENIChomozygous114060742
5154313919154313919G49GENIChomozygous128260287
5154314421154314422TC53GENIChomozygous114060744