chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 2,115863117,115863118,T,C,29,GENIC,homozygous,974911047 2,115866042,115866043,A,C,16,GENIC,homozygous,974911048 2,115866883,115866884,C,A,30,GENIC,homozygous,974911049 2,115867897,115867898,C,T,21,GENIC,homozygous,974911050 2,115869131,115869132,G,T,23,GENIC,homozygous,974911051 2,115869866,115869867,C,A,35,GENIC,homozygous,974911052 2,115872272,115872273,A,G,17,GENIC,homozygous,974911053 2,115875076,115875077,G,A,28,GENIC,homozygous,974911054 2,115876239,115876240,A,G,14,GENIC,homozygous,974911055 2,115877240,115877241,T,C,25,GENIC,possibly homozygous,974911056 2,115885838,115885839,C,G,30,GENIC,homozygous,974911057 2,115887019,115887020,A,C,20,GENIC,homozygous,974911058 2,115887991,115887992,A,C,33,GENIC,homozygous,974911059 2,115888567,115888568,C,T,19,GENIC,homozygous,974911060