chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,134857308,134857309,T,A,8,GENIC,homozygous,108344146 X,134857683,134857683,,GCA,11,GENIC,homozygous,129793583 X,134860497,134860505,TCTTTCTC,,9,GENIC,homozygous,129793584 X,134863073,134863074,A,G,7,GENIC,homozygous,108344150 X,134858892,134858893,A,G,7,GENIC,homozygous,108344148