chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 7,12606344,12606345,G,A,7,GENIC,homozygous,976010812 7,12606416,12606417,T,C,8,GENIC,homozygous,976010813 7,12607017,12607018,T,G,4,GENIC,homozygous,976010814 7,12607024,12607025,C,T,4,GENIC,homozygous,976010815 7,12607046,12607047,C,T,7,GENIC,homozygous,976010816 7,12607356,12607357,G,A,3,GENIC,homozygous,976010817 7,12607357,12607358,C,A,4,GENIC,homozygous,976010818 7,12607420,12607421,C,A,7,GENIC,homozygous,976010819 7,12607854,12607855,T,C,9,GENIC,homozygous,976010820 7,12608442,12608443,G,A,14,GENIC,homozygous,976010821 7,12609374,12609375,G,T,12,GENIC,homozygous,976010822 7,12609394,12609395,C,T,13,GENIC,homozygous,976010823 7,12609532,12609533,G,A,7,GENIC,homozygous,976010824 7,12609713,12609714,T,C,5,GENIC,homozygous,976010825