chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 5,9783828,9783829,A,C,12,GENIC,homozygous,978913215 5,9783864,9783865,T,C,14,GENIC,homozygous,978913216 5,9783898,9783899,C,G,14,GENIC,homozygous,978913217 5,9783906,9783907,A,G,13,GENIC,homozygous,978913218 5,9784329,9784330,T,A,18,GENIC,homozygous,978913219 5,9784359,9784360,T,C,21,GENIC,homozygous,978913220 5,9784448,9784449,T,C,10,GENIC,homozygous,978913221