chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 14,17616390,17616391,C,T,25,GENIC,homozygous,973722059 14,17616500,17616501,G,A,15,GENIC,homozygous,973722060 14,17616969,17616970,T,A,11,GENIC,homozygous,973722061 14,17617742,17617743,C,A,18,GENIC,homozygous,973722062 14,17619228,17619229,T,A,13,GENIC,homozygous,973722063 14,17620908,17620909,G,A,13,GENIC,homozygous,973722064 14,17621382,17621383,T,C,13,GENIC,homozygous,973722065 14,17621514,17621515,C,T,12,GENIC,homozygous,973722066 14,17622199,17622200,C,T,29,GENIC,homozygous,973722067 14,17622565,17622566,T,A,26,GENIC,homozygous,973722068 14,17625259,17625260,G,A,17,GENIC,homozygous,973722069 14,17625421,17625422,A,C,18,GENIC,homozygous,973722070 14,17625885,17625886,A,G,14,GENIC,homozygous,973722071 14,17627520,17627521,C,T,22,GENIC,homozygous,973722072 14,17629159,17629160,G,T,18,GENIC,homozygous,973722073 14,17630413,17630414,C,G,22,GENIC,homozygous,973722074