chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 5,56555209,56555210,C,A,9,GENIC,homozygous,978986165 5,56556100,56556101,T,G,23,GENIC,homozygous,978986166 5,56557394,56557395,T,C,46,GENIC,homozygous,978986167 5,56557724,56557725,C,T,39,GENIC,homozygous,978986168 5,56558072,56558073,G,A,33,GENIC,homozygous,978986169 5,56558375,56558376,T,C,34,GENIC,homozygous,978986170 5,56558838,56558839,A,T,15,GENIC,homozygous,978986171 5,56559926,56559927,G,A,14,GENIC,homozygous,978986172 5,56559941,56559942,A,C,11,GENIC,homozygous,978986173 5,56561004,56561005,A,G,39,GENIC,homozygous,978986174 5,56562080,56562081,C,T,28,GENIC,homozygous,978986175 5,56563187,56563188,T,C,54,GENIC,homozygous,978986176 5,56565399,56565400,T,A,70,GENIC,homozygous,978986177 5,56565837,56565838,C,T,20,GENIC,homozygous,978986178 5,56566169,56566170,T,C,33,GENIC,homozygous,978986179