chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 2,105016886,105016887,A,C,15,GENIC,homozygous,971907828 2,105019640,105019641,A,G,9,GENIC,homozygous,971907829 2,105020239,105020240,C,T,20,GENIC,homozygous,971907830 2,105020353,105020354,G,A,10,GENIC,homozygous,971907831 2,105027043,105027044,A,G,14,GENIC,homozygous,971907832 2,105027251,105027252,G,T,17,GENIC,homozygous,971907833 2,105027389,105027390,C,G,14,GENIC,homozygous,971907834 2,105029318,105029319,C,A,11,GENIC,homozygous,971907835 2,105029712,105029713,T,C,16,GENIC,homozygous,971907836 2,105035344,105035345,C,T,4,GENIC,heterozygous,971907837 2,105044760,105044761,A,T,8,GENIC,homozygous,971907838 2,105045764,105045765,T,G,11,GENIC,homozygous,971907839