chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 4,78320620,78320621,A,C,45,GENIC,homozygous,978789481 4,78323190,78323191,C,T,34,GENIC,homozygous,978789482 4,78323239,78323240,T,C,37,GENIC,homozygous,978789483 4,78325249,78325250,C,T,35,GENIC,homozygous,978789484 4,78325955,78325956,A,G,45,GENIC,homozygous,978789485