chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,153555542,153555543,T,G,12,GENIC,homozygous,977782630 X,153598162,153598163,T,G,7,GENIC,homozygous,977782631 X,153598807,153598808,G,A,15,GENIC,homozygous,977782632 X,153598810,153598811,C,A,14,GENIC,homozygous,977782633 X,153598870,153598871,C,A,10,GENIC,homozygous,977782634 X,153602136,153602137,C,T,15,GENIC,homozygous,977782635 X,153602157,153602158,C,T,18,GENIC,homozygous,977782636 X,153602220,153602221,C,T,12,GENIC,homozygous,977782637 X,153772165,153772166,G,T,15,GENIC,homozygous,977782638 X,153836513,153836514,T,G,14,GENIC,homozygous,977782639 X,154010336,154010337,T,C,6,GENIC,heterozygous,977782640 X,154021206,154021207,G,T,10,GENIC,heterozygous,977782641