chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 3,111735654,111735655,C,T,16,GENIC,homozygous,821517595 3,111735804,111735805,T,C,15,GENIC,homozygous,821517596 3,111735827,111735828,T,G,17,GENIC,homozygous,821517597 3,111735906,111735907,T,A,9,GENIC,homozygous,821517598 3,111736258,111736259,G,A,13,GENIC,homozygous,821517599 3,111736750,111736751,C,CA,19,GENIC,homozygous,821517600 3,111737037,111737038,G,A,22,GENIC,homozygous,821517601 3,111737191,111737192,G,C,18,GENIC,homozygous,821517602 3,111737599,111737600,C,CT,9,GENIC,homozygous,821517603 3,111737790,111737791,G,A,12,GENIC,homozygous,821517604 3,111739416,111739417,A,G,16,GENIC,homozygous,821517605 3,111739796,111739797,C,T,19,GENIC,homozygous,821517606 3,111740272,111740274,TC,--,12,GENIC,homozygous,821517607 3,111740639,111740640,A,C,16,GENIC,homozygous,821517608 3,111740640,111740641,T,C,16,GENIC,homozygous,821517609 3,111741074,111741075,C,T,14,GENIC,homozygous,821517610 3,111741114,111741115,C,CACTT,13,GENIC,homozygous,821517611 3,111741259,111741260,A,G,13,GENIC,homozygous,821517612 3,111741585,111741586,T,C,17,GENIC,homozygous,821517613 3,111741761,111741762,G,A,16,GENIC,homozygous,821517614 3,111741865,111741866,A,T,21,GENIC,homozygous,821517615 3,111742340,111742341,C,T,22,GENIC,homozygous,821517616