chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 6,137117007,137117008,G,A,16,GENIC,homozygous,975986040 6,137117454,137117455,C,T,9,GENIC,homozygous,975986041 6,137119884,137119885,C,T,10,GENIC,homozygous,975986042 6,137120235,137120236,C,A,20,GENIC,homozygous,975986043 6,137122371,137122372,A,G,18,GENIC,homozygous,975986044 6,137122491,137122492,C,A,30,GENIC,homozygous,975986045