chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 13,14579699,14579700,A,G,38,GENIC,homozygous,980115022 13,14579970,14579971,C,A,15,GENIC,homozygous,980115023 13,14580244,14580245,G,C,34,GENIC,homozygous,980115024 13,14580309,14580310,A,T,40,GENIC,homozygous,980115025 13,14580515,14580516,T,C,33,GENIC,homozygous,980115026 13,14580719,14580720,C,A,24,GENIC,homozygous,980115027 13,14580784,14580785,G,C,34,GENIC,homozygous,980115028 13,14580843,14580844,T,C,35,GENIC,homozygous,980115029 13,14580871,14580872,T,A,27,GENIC,homozygous,980115030 13,14580902,14580903,C,A,16,GENIC,homozygous,980115031 13,14580979,14580980,C,T,16,GENIC,homozygous,980115032 13,14581027,14581028,G,A,19,GENIC,homozygous,980115033 13,14581029,14581030,T,C,19,GENIC,homozygous,980115034 13,14581061,14581062,G,A,17,GENIC,homozygous,980115035