chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 5,33174616,33174617,A,G,14,GENIC,homozygous,975617051 5,33176371,33176372,G,A,6,GENIC,homozygous,975617052 5,33177051,33177052,A,C,10,GENIC,homozygous,975617053 5,33177542,33177543,G,A,9,GENIC,heterozygous,975617054 5,33177642,33177643,G,A,18,GENIC,heterozygous,975617055 5,33177668,33177669,C,A,17,GENIC,heterozygous,975617056 5,33177751,33177752,G,T,28,GENIC,heterozygous,975617057 5,33177994,33177995,G,A,10,GENIC,heterozygous,975617058 5,33178007,33178008,G,A,11,GENIC,heterozygous,975617059 5,33178080,33178081,G,A,17,GENIC,heterozygous,975617060 5,33178159,33178160,C,T,19,GENIC,heterozygous,975617061 5,33178210,33178211,C,G,19,GENIC,heterozygous,975617062 5,33178216,33178217,G,A,17,GENIC,heterozygous,975617063 5,33178221,33178222,A,G,18,GENIC,heterozygous,975617064 5,33178226,33178227,A,G,20,GENIC,heterozygous,975617065 5,33178231,33178232,G,T,20,GENIC,heterozygous,975617066 5,33179644,33179645,A,G,12,GENIC,homozygous,975617067 5,33180442,33180443,C,T,9,GENIC,homozygous,975617068 5,33180660,33180661,T,C,10,GENIC,homozygous,975617069 5,33180995,33180996,G,A,4,GENIC,homozygous,975617070