chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 17,90034065,90034066,T,C,24,GENIC,homozygous,974157573 17,90041552,90041553,C,T,9,GENIC,homozygous,974157574 17,90046134,90046135,A,G,16,GENIC,homozygous,974157575 17,90050057,90050058,A,T,22,GENIC,homozygous,974157576 17,90052333,90052334,G,A,5,GENIC,homozygous,974157577 17,90052396,90052397,G,T,9,GENIC,homozygous,974157578 17,90052736,90052737,A,C,17,GENIC,homozygous,974157579 17,90060823,90060824,A,T,13,GENIC,homozygous,974157580 17,90061246,90061247,A,G,20,GENIC,homozygous,974157581 17,90061297,90061298,C,G,16,GENIC,homozygous,974157582 17,90061541,90061542,T,G,10,GENIC,homozygous,974157583 17,90061559,90061560,A,C,10,GENIC,homozygous,974157584 17,90061992,90061993,T,G,10,GENIC,homozygous,974157585 17,90062102,90062103,A,G,19,GENIC,homozygous,974157586 17,90062347,90062348,A,T,8,GENIC,homozygous,974157587 17,90062348,90062349,T,A,8,GENIC,homozygous,974157588 17,90067658,90067659,A,G,15,GENIC,homozygous,974157589