chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5169293834169293835GT35GENIChomozygous114684402
5169306077169306078GA38GENIChomozygous114684404
5169316645169316645CT23GENIChomozygous128271495
5169316797169316797A28GENIChomozygous128271496
5169316799169316799C28GENIChomozygous128271497
5169316807169316808G26GENIChomozygous128271498
5169317346169317347C41GENIChomozygous128271499
5169319401169319402C29GENIChomozygous128271501
5169319404169319405TG29GENIChomozygous118937891
5169319405169319406CT29GENIChomozygous118937893
5169319419169319419T32GENIChomozygous128271502
5169319423169319425GC30GENIChomozygous128271503
5169319434169319435C28GENIChomozygous128271504
5169319439169319440A27GENIChomozygous128271505
5169319441169319442AC27GENIChomozygous118937895
5169319445169319446A26GENIChomozygous128271506
5169319465169319466A27GENIChomozygous128271507
5169316657169316775GCAAGGCGTCTACCACTGAGCTAAATCCCAAACCCTTGCCTCTGACTCTTAAGTGTTGGTATTAAAAGCAGGCATCAAAGGGTGTTGGGGATTTAGCTCAGCGGTAGAGCACTTGCTA42GENICheterozygous130552747
5169319450169319451AG27GENIChomozygous114163065
5169319457169319458AT26GENIChomozygous114163066
5169326232169326233CT31GENIChomozygous114604630