chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 18,62279071,62279072,A,G,23,GENIC,homozygous,974207650 18,62279284,62279285,C,T,19,GENIC,homozygous,974207651 18,62279394,62279395,A,G,21,GENIC,homozygous,974207652 18,62279435,62279436,C,T,26,GENIC,homozygous,974207653 18,62279446,62279447,C,T,25,GENIC,homozygous,974207654 18,62279544,62279545,T,C,25,GENIC,homozygous,974207655 18,62279589,62279590,A,G,25,GENIC,homozygous,974207656 18,62279608,62279609,C,A,28,GENIC,homozygous,974207657 18,62279629,62279630,G,A,23,GENIC,homozygous,974207658 18,62279676,62279677,T,C,17,GENIC,homozygous,974207659 18,62279715,62279716,T,C,17,GENIC,homozygous,974207660 18,62280553,62280554,T,A,18,GENIC,homozygous,974207661 18,62280743,62280744,C,T,14,GENIC,homozygous,974207662 18,62280795,62280796,T,C,18,GENIC,homozygous,974207663 18,62280801,62280802,A,G,20,GENIC,homozygous,974207664 18,62280824,62280825,T,C,18,GENIC,homozygous,974207665 18,62280890,62280891,T,C,12,GENIC,homozygous,974207666 18,62281059,62281060,G,C,12,GENIC,homozygous,974207667 18,62281334,62281335,C,T,15,GENIC,homozygous,974207668 18,62281608,62281609,A,T,12,GENIC,homozygous,974207669 18,62287111,62287112,T,A,11,GENIC,homozygous,974207670 18,62287274,62287275,A,G,26,GENIC,homozygous,974207671 18,62287300,62287301,T,C,25,GENIC,homozygous,974207672 18,62287356,62287357,C,T,22,GENIC,homozygous,974207673