chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,110901804,110901805,G,A,13,GENIC,homozygous,877786964 X,110906891,110906892,C,T,6,GENIC,homozygous,877786965 X,110906892,110906893,C,T,6,GENIC,homozygous,877786966 X,110911116,110911117,C,A,12,GENIC,homozygous,877786967 X,110917889,110917890,A,G,4,GENIC,heterozygous,877786968 X,110937504,110937505,T,G,4,GENIC,homozygous,877786969 X,110944090,110944091,C,A,10,GENIC,homozygous,877786970 X,110944305,110944306,G,A,4,GENIC,homozygous,877786971 X,110944306,110944307,C,G,4,GENIC,homozygous,877786972 X,110944345,110944346,A,G,5,GENIC,homozygous,877786973 X,110961870,110961871,C,A,3,GENIC,heterozygous,877786974 X,110969698,110969699,C,A,13,GENIC,homozygous,877786975 X,110974447,110974448,A,T,14,GENIC,heterozygous,877786976