chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,78212956,78212957,C,G,49,GENIC,homozygous,977862723 1,78213759,78213760,G,A,21,GENIC,homozygous,977862724 1,78214038,78214039,T,A,34,GENIC,homozygous,977862725 1,78214598,78214599,G,A,86,GENIC,homozygous,977862726 1,78216792,78216793,A,G,28,GENIC,homozygous,977862727 1,78217899,78217900,T,C,79,GENIC,homozygous,977862728 1,78218317,78218318,T,G,47,GENIC,homozygous,977862729 1,78218342,78218343,G,T,45,GENIC,homozygous,977862730 1,78218413,78218414,T,C,29,GENIC,homozygous,977862731 1,78218911,78218912,A,C,35,GENIC,homozygous,977862732 1,78219252,78219253,G,T,11,GENIC,homozygous,977862733 1,78219854,78219855,T,C,38,GENIC,homozygous,977862734 1,78219855,78219856,C,T,39,GENIC,homozygous,977862735 1,78220015,78220016,T,C,33,GENIC,homozygous,977862736 1,78220052,78220053,C,T,52,GENIC,homozygous,977862737 1,78220696,78220697,A,G,46,GENIC,homozygous,977862738 1,78220983,78220984,A,G,30,GENIC,homozygous,977862739 1,78221431,78221432,A,G,51,GENIC,homozygous,977862740