chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 13,70259663,70259664,T,C,19,GENIC,homozygous,976897443 13,70267315,70267316,C,T,20,GENIC,homozygous,976897444 13,70268144,70268145,G,A,29,GENIC,homozygous,976897445 13,70268502,70268503,C,A,26,GENIC,homozygous,976897446 13,70271850,70271851,T,C,28,GENIC,homozygous,976897447 13,70275508,70275509,A,T,35,GENIC,homozygous,976897448 13,70276003,70276004,G,A,23,GENIC,homozygous,976897449 13,70276129,70276130,T,C,26,GENIC,homozygous,976897450 13,70279547,70279548,T,C,9,GENIC,homozygous,976897451 13,70282350,70282351,C,G,20,GENIC,homozygous,976897452 13,70284762,70284763,C,T,23,GENIC,homozygous,976897453 13,70293266,70293267,C,T,27,GENIC,homozygous,976897454 13,70296515,70296516,C,T,30,GENIC,homozygous,976897455 13,70306721,70306722,T,C,32,GENIC,homozygous,976897456