chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,37492281,37492282,C,CT,8,INTERGENIC,homozygous,45125151 X,37498990,37498991,G,-,4,INTERGENIC,heterozygous,45125156 X,37499006,37499007,G,GT,1,INTERGENIC,homozygous,45254618 X,37499008,37499009,A,G,1,INTERGENIC,homozygous,45506743 X,37499011,37499012,G,-,1,INTERGENIC,homozygous,45254619 X,37499114,37499115,C,CA,2,INTERGENIC,homozygous,45125159 X,37542122,37542123,T,-,5,GENIC,heterozygous,45125165 X,37567267,37567268,T,-,4,INTERGENIC,heterozygous,45436862