chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 14,21592967,21592968,G,C,30,GENIC,homozygous,976963404 14,21593478,21593479,T,C,22,GENIC,homozygous,976963405 14,21593543,21593544,A,C,24,GENIC,homozygous,976963406 14,21593819,21593820,C,T,25,GENIC,homozygous,976963407 14,21596419,21596420,T,C,20,GENIC,homozygous,976963408 14,21603159,21603160,T,A,27,GENIC,homozygous,976963409 14,21603665,21603666,A,C,30,GENIC,homozygous,976963410 14,21604167,21604168,C,A,25,GENIC,homozygous,976963411 14,21604636,21604637,T,C,34,GENIC,heterozygous,976963412 14,21604694,21604695,T,C,48,GENIC,heterozygous,976963413 14,21604696,21604697,T,C,48,GENIC,heterozygous,976963414 14,21604710,21604711,G,T,46,GENIC,heterozygous,976963415 14,21604713,21604714,A,C,46,GENIC,heterozygous,976963416 14,21604717,21604718,A,G,46,GENIC,heterozygous,976963417 14,21604725,21604726,A,G,46,GENIC,heterozygous,976963418 14,21605152,21605153,T,C,20,GENIC,homozygous,976963419