chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,46977813,46977814,C,T,9,GENIC,homozygous,971469482 X,46978965,46978966,G,T,14,GENIC,homozygous,971469483 X,46978977,46978978,G,A,13,GENIC,homozygous,971469484 X,46978978,46978979,A,G,13,GENIC,homozygous,971469485 X,46995399,46995400,A,C,9,GENIC,homozygous,971469486 X,47004296,47004297,G,A,10,GENIC,homozygous,971469487 X,47009839,47009840,A,G,8,GENIC,homozygous,971469488 X,47010768,47010769,G,A,8,GENIC,homozygous,971469489 X,47011337,47011338,C,A,3,GENIC,homozygous,971469490 X,47011466,47011467,A,G,5,GENIC,homozygous,971469491 X,47011814,47011815,C,T,9,GENIC,homozygous,971469492 X,47014863,47014864,A,C,8,GENIC,homozygous,971469493 X,47018763,47018764,C,T,16,GENIC,homozygous,971469494 X,47022045,47022046,G,A,16,GENIC,homozygous,971469495 X,47024308,47024309,A,T,6,GENIC,homozygous,971469496 X,47025892,47025893,T,C,8,GENIC,homozygous,971469497 X,47026357,47026358,C,T,9,GENIC,homozygous,971469498