chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 10,104690272,104690273,C,T,14,GENIC,heterozygous,828577013 10,104690382,104690383,C,T,9,GENIC,heterozygous,828577014 10,104690434,104690435,G,C,11,GENIC,heterozygous,828577015 10,104690694,104690695,A,G,10,GENIC,heterozygous,828577016 10,104690707,104690708,A,T,9,GENIC,heterozygous,828577017 10,104690806,104690807,G,A,15,GENIC,heterozygous,828577018 10,104690958,104690959,A,G,10,GENIC,heterozygous,828577019 10,104691059,104691060,T,C,10,GENIC,homozygous,828577020 10,104691279,104691280,A,AAC,14,GENIC,heterozygous,828577021 10,104691319,104691321,CA,--,10,GENIC,homozygous,828577022 10,104691681,104691682,C,A,17,GENIC,heterozygous,828577023 10,104691775,104691776,A,T,12,GENIC,heterozygous,828577024 10,104691980,104691981,G,A,14,GENIC,heterozygous,828577025 10,104692097,104692098,C,T,20,GENIC,heterozygous,828577026 10,104692126,104692127,G,A,20,GENIC,heterozygous,828577027 10,104692195,104692196,T,C,14,GENIC,heterozygous,828577028