chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 17,43680583,43680584,T,C,29,GENIC,homozygous,971162493 17,43680897,43680898,A,G,25,GENIC,homozygous,971162494 17,43680999,43681000,C,T,19,GENIC,homozygous,971162495 17,43681261,43681262,G,A,18,GENIC,homozygous,971162496 17,43681262,43681263,A,T,18,GENIC,homozygous,971162497 17,43681648,43681649,G,A,37,GENIC,homozygous,971162498 17,43681649,43681650,C,A,37,GENIC,homozygous,971162499 17,43681656,43681657,G,A,38,GENIC,homozygous,971162500 17,43682451,43682452,C,G,36,GENIC,homozygous,971162501 17,43683383,43683384,T,C,17,GENIC,homozygous,971162502 17,43683980,43683981,C,A,24,GENIC,homozygous,971162503 17,43684368,43684369,T,C,19,GENIC,homozygous,971162504 17,43684386,43684387,C,A,17,GENIC,homozygous,971162505 17,43686692,43686693,T,C,22,GENIC,homozygous,971162506 17,43686736,43686737,T,C,21,GENIC,homozygous,971162507 17,43686847,43686848,A,G,15,GENIC,homozygous,971162508 17,43686935,43686936,T,C,10,GENIC,homozygous,971162509 17,43687771,43687772,G,T,27,GENIC,homozygous,971162510 17,43687817,43687818,A,C,29,GENIC,homozygous,971162511 17,43688737,43688738,C,A,25,GENIC,homozygous,971162512 17,43688749,43688750,G,A,28,GENIC,homozygous,971162513 17,43689225,43689226,G,C,32,GENIC,homozygous,971162514 17,43689231,43689232,A,T,32,GENIC,homozygous,971162515