chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 14,17618471,17618472,T,A,22,GENIC,homozygous,976955533 14,17621382,17621383,T,C,36,GENIC,homozygous,976955534 14,17622565,17622566,T,A,33,GENIC,homozygous,976955535 14,17623059,17623060,T,C,12,GENIC,homozygous,976955536 14,17624364,17624365,C,T,24,GENIC,homozygous,976955537 14,17624390,17624391,T,C,28,GENIC,homozygous,976955538 14,17625497,17625498,A,C,19,GENIC,heterozygous,976955539 14,17625885,17625886,A,G,20,GENIC,homozygous,976955540 14,17627090,17627091,C,A,33,GENIC,homozygous,976955541 14,17629159,17629160,G,T,11,GENIC,homozygous,976955542 14,17629804,17629805,A,G,28,GENIC,homozygous,976955543 14,17629805,17629806,C,A,27,GENIC,homozygous,976955544 14,17629810,17629811,A,G,27,GENIC,homozygous,976955545 14,17631409,17631410,C,T,26,GENIC,homozygous,976955546