chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 16,70905462,70905463,T,TTACTTTGGATTGACACCAAAGTCGCTGCCAGAATAGTTTGGAGGCTGCTGCACGGACAGGTGCTAACCAGACGAG,8,GENIC,homozygous,732371723 16,70911383,70911384,G,C,3,GENIC,heterozygous,607970074 16,70919494,70919495,A,AGCTCATGTTGTAGCTCAG,32,GENIC,homozygous,732371725