chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161024754161024755AG46GENIChomozygous55816867
5161024834161024835G-51GENIChomozygous55816868
5161025139161025140GA47GENIChomozygous55816869
5161025148161025149C-42GENIChomozygous55816870
5161025784161025785GA61GENIChomozygous55816871
5161026048161026049C-19GENIChomozygous55816872
5161026056161026057CCA28GENICpossibly homozygous55816873
5161026345161026346CT62GENIChomozygous55816874
5161026388161026389AC62GENIChomozygous55816875
5161026563161026564CCCACTTT34GENIChomozygous55816876
5161026610161026611GA50GENIChomozygous55816877