chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,46977813,46977814,C,T,6,GENIC,homozygous,887080776 X,46982977,46982978,C,T,10,GENIC,homozygous,887080777 X,46991579,46991580,G,C,9,GENIC,heterozygous,887080772 X,46994741,46994742,G,C,3,GENIC,heterozygous,887080773 X,46997510,46997511,C,A,5,GENIC,heterozygous,887078014 X,46997511,46997512,G,T,5,GENIC,heterozygous,887078013 X,47008414,47008415,A,T,3,GENIC,heterozygous,887080778 X,47009839,47009840,A,G,14,GENIC,homozygous,887080779 X,47010768,47010769,G,A,5,GENIC,homozygous,887080780 X,47014852,47014853,C,A,7,GENIC,homozygous,887080781 X,47014863,47014864,A,C,6,GENIC,homozygous,887080782 X,47014884,47014885,T,C,4,GENIC,homozygous,887080783 X,47015005,47015006,A,T,9,GENIC,homozygous,887080784 X,47016720,47016721,C,G,5,GENIC,homozygous,887080785 X,47018763,47018764,C,T,15,GENIC,homozygous,887080786 X,47022045,47022046,G,A,13,GENIC,homozygous,887080787 X,47024308,47024309,A,T,5,GENIC,heterozygous,887080788 X,47025892,47025893,T,C,8,GENIC,homozygous,887080789 X,47026357,47026358,C,T,11,GENIC,homozygous,887080790