chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 3,176416778,176416779,A,C,24,GENIC,homozygous,978686199 3,176417058,176417059,C,T,16,GENIC,homozygous,978686200 3,176417847,176417848,T,A,65,GENIC,homozygous,978686201 3,176420655,176420656,A,T,22,GENIC,homozygous,978686202 3,176421058,176421059,C,T,51,GENIC,homozygous,978686203 3,176423063,176423064,T,C,35,GENIC,homozygous,978686204 3,176423384,176423385,G,A,30,GENIC,homozygous,978686205 3,176423703,176423704,A,G,24,GENIC,homozygous,978686206 3,176424176,176424177,G,A,29,GENIC,homozygous,978686207 3,176426813,176426814,A,G,29,GENIC,homozygous,978686208 3,176430018,176430019,C,G,24,GENIC,homozygous,978686209 3,176430050,176430051,A,C,42,GENIC,homozygous,978686210 3,176430869,176430870,C,A,39,GENIC,homozygous,978686211 3,176431217,176431218,T,C,87,GENIC,homozygous,978686212