chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 12,40262600,40262601,C,CT,4,GENIC,heterozygous,50202955 12,40262600,40262601,C,CTTTTTTT,4,GENIC,heterozygous,50543564 12,40263348,40263349,A,G,10,GENIC,homozygous,50202956 12,40263691,40263692,G,GTT,5,GENIC,homozygous,50571675 12,40265417,40265418,T,C,12,GENIC,homozygous,50202959 12,40265648,40265649,C,A,7,GENIC,homozygous,50512395