chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 7,12606344,12606345,G,A,17,GENIC,homozygous,896139629 7,12606416,12606417,T,C,4,GENIC,homozygous,896139630 7,12606947,12606948,A,T,7,GENIC,homozygous,896139631 7,12606957,12606958,G,A,8,GENIC,homozygous,896139632 7,12607017,12607018,T,G,7,GENIC,homozygous,896139633 7,12607024,12607025,C,T,4,GENIC,homozygous,896139634 7,12607316,12607317,A,G,7,GENIC,homozygous,896139635 7,12607420,12607421,C,A,15,GENIC,homozygous,896139636 7,12607854,12607855,T,C,13,GENIC,homozygous,896139637 7,12608061,12608062,G,C,14,GENIC,homozygous,896139638 7,12608442,12608443,G,A,18,GENIC,homozygous,896139639 7,12609374,12609375,G,T,12,GENIC,homozygous,896139640 7,12609394,12609395,C,T,15,GENIC,homozygous,896139641 7,12609713,12609714,T,C,12,GENIC,homozygous,896139642