chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 7,144103342,144103343,C,G,23,GENIC,homozygous,979485628 7,144103528,144103529,T,C,20,GENIC,homozygous,979485629 7,144105165,144105166,T,G,27,GENIC,homozygous,979485630 7,144107661,144107662,A,G,66,GENIC,homozygous,979485631 7,144107952,144107953,C,T,51,GENIC,homozygous,979485632 7,144109385,144109386,T,C,29,GENIC,homozygous,979485633 7,144109598,144109599,C,G,55,GENIC,homozygous,979485634 7,144109629,144109630,C,T,59,GENIC,homozygous,979485635 7,144109681,144109682,A,C,55,GENIC,homozygous,979485636 7,144110529,144110530,C,T,44,GENIC,homozygous,979485637 7,144110901,144110902,A,C,54,GENIC,homozygous,979485638 7,144111438,144111439,T,C,29,GENIC,homozygous,979485639 7,144112053,144112054,G,A,42,GENIC,homozygous,979485640 7,144112570,144112571,T,C,48,GENIC,homozygous,979485641 7,144115195,144115196,C,T,40,GENIC,homozygous,979485642 7,144115606,144115607,A,G,46,GENIC,homozygous,979485643 7,144115720,144115721,G,A,34,GENIC,homozygous,979485644 7,144115776,144115777,G,A,30,GENIC,homozygous,979485645 7,144116204,144116205,G,A,42,GENIC,homozygous,979485646 7,144116838,144116839,G,A,29,GENIC,homozygous,979485647 7,144116920,144116921,T,C,25,GENIC,homozygous,979485648