chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 2681980 2681981 T G 11 GENIC possibly homozygous 547399669 8 2683971 2683972 T C 2 GENIC homozygous 547399670 8 2684089 2684090 T G 3 GENIC homozygous 547399671 8 2684911 2684912 G A 1 GENIC homozygous 548624307 8 2685018 2685019 C T 10 GENIC homozygous 547399672 8 2686918 2686919 T C 15 GENIC possibly homozygous 548624308 8 2688856 2688857 G A 6 GENIC homozygous 548624309 8 2689308 2689309 T C 14 GENIC homozygous 547399673 8 2690266 2690267 C T 10 GENIC homozygous 547399674 8 2692231 2692232 T - 5 GENIC heterozygous 699087890 8 2694493 2694494 C T 12 GENIC possibly homozygous 548624310 8 2694648 2694649 A AT 2 GENIC homozygous 699087891 8 2697970 2697971 T A 5 GENIC homozygous 547399675 8 2699630 2699631 C T 15 GENIC homozygous 548624311 8 2701816 2701817 C T 12 GENIC homozygous 548624312 8 2704786 2704787 G A 28 GENIC homozygous 548624313 8 2706973 2706974 A G 16 GENIC possibly homozygous 548624314 8 2707919 2707920 T - 1 GENIC homozygous 699087892 8 2708043 2708044 C T 4 GENIC homozygous 548624315 8 2708180 2708181 T C 18 GENIC homozygous 548624316 8 2710158 2710159 T G 5 GENIC homozygous 548624317