chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,245478671,245478672,C,T,25,GENIC,homozygous,978043333 1,245482925,245482926,T,G,47,GENIC,homozygous,978043334 1,245484706,245484707,A,G,31,GENIC,homozygous,978043335 1,245484741,245484742,A,C,36,GENIC,homozygous,978043336 1,245485884,245485885,C,G,48,GENIC,homozygous,978043337 1,245487389,245487390,T,C,5,GENIC,homozygous,978043338 1,245487458,245487459,G,A,14,GENIC,homozygous,978043339 1,245489679,245489680,G,T,41,GENIC,homozygous,978043340 1,245500482,245500483,A,G,14,GENIC,homozygous,978043341 1,245501182,245501183,T,A,45,GENIC,homozygous,978043342 1,245501635,245501636,A,T,27,GENIC,homozygous,978043343 1,245503750,245503751,G,A,40,GENIC,homozygous,978043344 1,245507013,245507014,T,C,22,GENIC,homozygous,978043345 1,245508345,245508346,T,C,26,GENIC,homozygous,978043346 1,245508617,245508618,G,A,27,GENIC,homozygous,978043347 1,245509605,245509606,G,A,32,GENIC,homozygous,978043348 1,245510582,245510583,C,T,34,GENIC,homozygous,978043349 1,245515748,245515749,A,G,18,GENIC,homozygous,978043350 1,245516179,245516180,A,G,54,GENIC,homozygous,978043351