chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,101955796,101955797,C,CTT,8,INTERGENIC,possibly homozygous,60779919 1,101961278,101961279,G,GT,22,GENIC,homozygous,60779921 1,101969969,101969970,G,GT,10,GENIC,possibly homozygous,60779922 1,101977351,101977352,A,-,4,GENIC,heterozygous,62229267 1,101996693,101996694,T,TTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGC,12,GENIC,homozygous,62147192