chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 14,24103800,24103801,T,G,7,GENIC,homozygous,976968683 14,24103859,24103860,T,A,19,GENIC,homozygous,976968684 14,24104271,24104272,T,C,30,GENIC,homozygous,976968685 14,24104367,24104368,T,C,34,GENIC,homozygous,976968686 14,24104416,24104417,G,C,29,GENIC,homozygous,976968687 14,24104564,24104565,G,A,27,GENIC,homozygous,976968688 14,24104718,24104719,G,A,32,GENIC,homozygous,976968689 14,24104742,24104743,T,C,39,GENIC,homozygous,976968690 14,24109614,24109615,T,C,25,GENIC,homozygous,976968691 14,24109642,24109643,C,T,26,GENIC,homozygous,976968692 14,24109823,24109824,G,T,24,GENIC,homozygous,976968693 14,24109894,24109895,G,T,17,GENIC,homozygous,976968694 14,24109990,24109991,G,C,14,GENIC,homozygous,976968695 14,24116090,24116091,C,G,8,GENIC,homozygous,976968696 14,24116537,24116538,T,C,29,GENIC,homozygous,976968697 14,24116710,24116711,G,A,42,GENIC,homozygous,976968698 14,24117045,24117046,A,C,32,GENIC,homozygous,976968699 14,24119438,24119439,T,A,21,GENIC,homozygous,976968700 14,24119888,24119889,G,A,31,GENIC,homozygous,976968701 14,24120286,24120287,G,A,22,GENIC,homozygous,976968702 14,24121237,24121238,G,A,25,GENIC,homozygous,976968703 14,24121487,24121488,G,A,41,GENIC,homozygous,976968704 14,24121869,24121870,A,T,34,GENIC,homozygous,976968705 14,24123292,24123293,G,T,27,GENIC,homozygous,976968706 14,24123313,24123314,G,C,31,GENIC,homozygous,976968707 14,24123891,24123892,G,C,39,GENIC,homozygous,976968708 14,24124628,24124629,A,G,19,GENIC,homozygous,976968709 14,24125242,24125243,T,C,34,GENIC,homozygous,976968710