chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,33090842,33090846,ACAT,----,5,GENIC,homozygous,742801127 X,33093205,33093207,CT,--,8,GENIC,heterozygous,742801129 X,33105112,33105114,AC,--,1,GENIC,homozygous,742801133 X,33108382,33108383,G,A,8,GENIC,homozygous,619102363 X,33111352,33111355,TGT,---,3,GENIC,heterozygous,742801138