chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 24103800 24103801 T G 16 INTERGENIC homozygous 804607671 14 24104201 24104202 C G 11 GENIC homozygous 804607672 14 24104432 24104433 G T 15 GENIC homozygous 804607673 14 24104446 24104447 G A 15 GENIC possibly homozygous 804607674 14 24104564 24104565 G A 12 GENIC homozygous 804607675 14 24104718 24104719 G A 14 GENIC homozygous 804607676 14 24104742 24104743 T C 13 GENIC homozygous 804607677 14 24105457 24105458 T C 26 GENIC homozygous 804607678 14 24105596 24105597 C T 19 GENIC homozygous 804607679 14 24107412 24107413 A G 9 GENIC homozygous 804607680 14 24108415 24108416 T C 4 GENIC homozygous 804607681 14 24108780 24108781 A G 9 GENIC homozygous 804607682 14 24109666 24109667 A G 12 GENIC homozygous 804607683 14 24116090 24116091 C G 10 GENIC homozygous 804607684 14 24116537 24116538 T C 14 GENIC homozygous 804607685 14 24119438 24119439 T A 19 GENIC homozygous 804607686 14 24119888 24119889 G A 9 GENIC homozygous 804607687 14 24120286 24120287 G A 13 GENIC homozygous 804607688 14 24120986 24120987 C T 10 GENIC homozygous 804607689 14 24121053 24121054 T A 5 GENIC homozygous 804607690 14 24121237 24121238 G A 14 GENIC homozygous 804607691 14 24121487 24121488 G A 14 GENIC homozygous 804607692 14 24122422 24122423 C T 26 GENIC possibly homozygous 804607693 14 24122434 24122435 A G 27 GENIC possibly homozygous 804607694 14 24123292 24123293 G T 24 GENIC homozygous 804607695 14 24123313 24123314 G C 20 GENIC homozygous 804607696 14 24123891 24123892 G C 12 GENIC homozygous 804607697 14 24124628 24124629 A G 17 GENIC homozygous 804607698 14 24124815 24124816 C T 13 GENIC homozygous 804607699 14 24125242 24125243 T C 14 GENIC homozygous 804607700