chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 9,49837919,49837920,A,G,34,GENIC,homozygous,979715651 9,49837998,49837999,C,A,31,GENIC,homozygous,979715652 9,49838206,49838207,G,A,77,GENIC,possibly homozygous,979715653 9,49838323,49838324,A,G,93,GENIC,homozygous,979715654 9,49838842,49838843,T,C,64,GENIC,homozygous,979715655 9,49839100,49839101,A,G,42,GENIC,homozygous,979715656 9,49839148,49839149,C,T,39,GENIC,homozygous,979715657 9,49839609,49839610,T,C,33,GENIC,homozygous,979715658 9,49839626,49839627,A,T,33,GENIC,homozygous,979715659 9,49839694,49839695,A,G,27,GENIC,homozygous,979715660 9,49839808,49839809,G,T,21,GENIC,homozygous,979715661 9,49840237,49840238,G,A,58,GENIC,homozygous,979715662 9,49840670,49840671,T,G,34,GENIC,homozygous,979715663 9,49840704,49840705,G,C,43,GENIC,homozygous,979715664 9,49840777,49840778,A,T,62,GENIC,homozygous,979715665 9,49840981,49840982,A,G,59,GENIC,homozygous,979715666 9,49841053,49841054,G,C,48,GENIC,homozygous,979715667 9,49841076,49841077,A,G,40,GENIC,homozygous,979715668 9,49841092,49841093,G,A,35,GENIC,homozygous,979715669 9,49841119,49841120,T,C,27,GENIC,homozygous,979715670 9,49841160,49841161,A,G,17,GENIC,homozygous,979715671 9,49841232,49841233,A,C,13,GENIC,homozygous,979715672