chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 17,90034065,90034066,T,C,24,GENIC,homozygous,971219764 17,90041552,90041553,C,T,36,GENIC,homozygous,971219765 17,90046134,90046135,A,G,19,GENIC,homozygous,971219766 17,90050057,90050058,A,T,19,GENIC,homozygous,971219767 17,90052396,90052397,G,T,15,GENIC,homozygous,971219768 17,90052422,90052423,C,T,18,GENIC,homozygous,971219769 17,90052642,90052643,G,T,19,GENIC,homozygous,971219770 17,90052736,90052737,A,C,31,GENIC,homozygous,971219771 17,90060823,90060824,A,T,22,GENIC,homozygous,971219772 17,90061246,90061247,A,G,21,GENIC,homozygous,971219773 17,90061297,90061298,C,G,21,GENIC,homozygous,971219774 17,90061541,90061542,T,G,17,GENIC,homozygous,971219775 17,90061559,90061560,A,C,15,GENIC,homozygous,971219776 17,90061992,90061993,T,G,21,GENIC,homozygous,971219777 17,90062102,90062103,A,G,15,GENIC,homozygous,971219778 17,90062347,90062348,A,T,20,GENIC,homozygous,971219779 17,90062348,90062349,T,A,20,GENIC,homozygous,971219780 17,90067658,90067659,A,G,18,GENIC,homozygous,971219781