chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 3,125175833,125175834,T,C,15,GENIC,homozygous,978626758 3,125177947,125177948,A,G,32,GENIC,homozygous,978626759 3,125178727,125178728,T,C,9,GENIC,homozygous,978626760 3,125179757,125179758,A,C,28,GENIC,homozygous,978626761 3,125182814,125182815,T,C,55,GENIC,homozygous,978626762 3,125183301,125183302,C,T,9,GENIC,homozygous,978626763 3,125183719,125183720,G,A,36,GENIC,homozygous,978626764 3,125189281,125189282,A,T,23,GENIC,homozygous,978626765 3,125189784,125189785,C,T,34,GENIC,homozygous,978626766 3,125190594,125190595,G,A,18,GENIC,homozygous,978626767 3,125192028,125192029,T,A,11,GENIC,homozygous,978626768 3,125192032,125192033,G,T,10,GENIC,homozygous,978626769 3,125203732,125203733,C,G,28,GENIC,homozygous,978626770 3,125203830,125203831,C,T,13,GENIC,homozygous,978626771 3,125205153,125205154,G,A,20,GENIC,homozygous,978626772 3,125207297,125207298,A,G,36,GENIC,homozygous,978626773 3,125208240,125208241,G,A,19,GENIC,homozygous,978626774 3,125208822,125208823,C,T,27,GENIC,homozygous,978626775 3,125209924,125209925,A,G,36,GENIC,homozygous,978626776 3,125210208,125210209,T,C,13,GENIC,homozygous,978626777 3,125212352,125212353,G,A,6,GENIC,homozygous,978626778