chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 92025498 92025499 C T 25 GENIC homozygous 813212878 10 92026302 92026303 C T 17 GENIC homozygous 813212879 10 92026777 92026778 C T 16 GENIC homozygous 813212880 10 92028059 92028060 T A 8 GENIC homozygous 813212881 10 92028106 92028107 A G 14 GENIC homozygous 813212882 10 92029589 92029590 T A 5 GENIC heterozygous 813212883 10 92029769 92029770 A G 8 GENIC homozygous 813212884 10 92029782 92029783 G A 10 GENIC homozygous 813212885 10 92029897 92029898 A G 20 GENIC homozygous 813212886 10 92029899 92029900 G T 20 GENIC homozygous 813212887 10 92030733 92030734 T C 26 GENIC homozygous 813212888 10 92031000 92031001 T A 28 GENIC homozygous 813212889 10 92031020 92031021 C T 30 GENIC homozygous 813212890 10 92031036 92031037 C A 31 GENIC possibly homozygous 813212891 10 92031231 92031232 G A 17 GENIC homozygous 813212892 10 92031353 92031354 A T 23 GENIC homozygous 813212893 10 92031467 92031468 G C 27 GENIC homozygous 813212894 10 92031653 92031654 T C 20 GENIC possibly homozygous 813212895 10 92032722 92032723 C A 27 GENIC homozygous 813212896 10 92032794 92032795 C T 20 GENIC homozygous 813212897 10 92033006 92033007 T C 23 GENIC homozygous 813212898 10 92034140 92034141 C G 24 GENIC homozygous 813212899 10 92034438 92034439 C T 29 GENIC homozygous 813212900 10 92035331 92035332 C G 20 GENIC homozygous 813212901 10 92037326 92037327 C T 32 GENIC homozygous 813212902 10 92037519 92037520 T C 22 GENIC homozygous 813212903 10 92039540 92039541 G T 21 GENIC homozygous 813212904 10 92040134 92040135 C T 29 GENIC homozygous 813212905