chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,40782666,40782667,A,G,11,GENIC,homozygous,578149722 X,40798738,40798739,C,CA,2,GENIC,heterozygous,717871105 X,40875565,40875566,G,T,1,GENIC,homozygous,580821108 X,40875567,40875568,C,-,1,GENIC,homozygous,717871107 X,40875688,40875689,G,A,5,GENIC,homozygous,578149723 X,40875696,40875697,T,A,8,GENIC,homozygous,578149724 X,40875698,40875699,A,T,9,GENIC,homozygous,578149725 X,40883913,40883914,G,GTT,1,GENIC,homozygous,717871108 X,40901439,40901441,TG,--,7,GENIC,heterozygous,717871110 X,40903271,40903272,A,-,2,GENIC,homozygous,717871112 X,40932283,40932284,A,AGTT,2,GENIC,homozygous,717871113 X,40941400,40941401,T,C,10,GENIC,homozygous,580821109 X,40941407,40941408,A,AC,11,GENIC,homozygous,717871114 X,40969061,40969062,C,CT,4,GENIC,heterozygous,717871115 X,40994259,40994260,C,T,1,GENIC,homozygous,578149726 X,40994262,40994263,C,T,1,GENIC,homozygous,578149727 X,41017232,41017233,G,T,7,GENIC,homozygous,578149728 X,41017256,41017257,G,T,2,GENIC,homozygous,578149729 X,41017257,41017258,A,AACAC,2,GENIC,homozygous,717871116 X,41017261,41017265,CTTT,----,2,GENIC,homozygous,717871117 X,41017315,41017316,C,-,7,GENIC,homozygous,717871118 X,41018317,41018318,G,-,9,GENIC,heterozygous,717871119