chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,104768468,104768471,TTC,---,1,INTERGENIC,homozygous,45264097 X,104768838,104768839,T,TC,13,INTERGENIC,homozygous,45189995 X,104778231,104778232,T,G,23,INTERGENIC,heterozygous,45440124 X,104802743,104802744,C,CAAA,16,GENIC,homozygous,45189996 X,104802746,104802747,C,CA,14,GENIC,homozygous,45189997