chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,245478671,245478672,C,T,32,GENIC,homozygous,974698266 1,245480598,245480599,A,T,20,GENIC,homozygous,974698267 1,245480625,245480626,C,T,26,GENIC,homozygous,974698268 1,245482925,245482926,T,G,30,GENIC,homozygous,974698269 1,245484706,245484707,A,G,27,GENIC,homozygous,974698270 1,245484741,245484742,A,C,25,GENIC,homozygous,974698271 1,245485884,245485885,C,G,17,GENIC,homozygous,974698272 1,245487389,245487390,T,C,36,GENIC,homozygous,974698273 1,245487458,245487459,G,A,41,GENIC,homozygous,974698274 1,245489679,245489680,G,T,25,GENIC,homozygous,974698275 1,245500482,245500483,A,G,28,GENIC,homozygous,974698276 1,245501182,245501183,T,A,24,GENIC,homozygous,974698277 1,245501635,245501636,A,T,39,GENIC,homozygous,974698278 1,245507013,245507014,T,C,35,GENIC,homozygous,974698279 1,245508345,245508346,T,C,24,GENIC,homozygous,974698280 1,245508617,245508618,G,A,12,GENIC,homozygous,974698281 1,245509605,245509606,G,A,26,GENIC,homozygous,974698282 1,245515748,245515749,A,G,30,GENIC,homozygous,974698283 1,245516179,245516180,A,G,27,GENIC,homozygous,974698284