chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 38105020 38105021 A T 103 GENIC heterozygous 506071821 8 38105063 38105064 A G 88 GENIC heterozygous 506071822 8 38105069 38105070 T A 84 GENIC heterozygous 506071823 8 38105095 38105096 C T 97 GENIC heterozygous 506071824 8 38105105 38105106 T C 86 GENIC heterozygous 506071825 8 38105109 38105110 A C 86 GENIC heterozygous 506071826 8 38105173 38105174 G A 97 GENIC heterozygous 506071827 8 38105372 38105373 T C 101 GENIC heterozygous 506071828 8 38105377 38105378 A G 98 GENIC heterozygous 506071829 8 38105389 38105390 T C 101 GENIC heterozygous 506071830 8 38105479 38105480 G A 122 GENIC heterozygous 506071831 8 38105697 38105698 G C 41 GENIC heterozygous 506071832 8 38105718 38105719 T G 49 GENIC heterozygous 506071833 8 38105722 38105723 A G 52 GENIC heterozygous 506071834 8 38105730 38105731 C T 54 GENIC heterozygous 506071835 8 38105751 38105752 A C 47 GENIC heterozygous 506071836 8 38105753 38105754 T G 50 GENIC heterozygous 506071837 8 38105759 38105760 A G 56 GENIC heterozygous 506071838 8 38105788 38105789 C T 76 GENIC heterozygous 506071839 8 38105981 38105982 C T 79 GENIC heterozygous 506071840 8 38105996 38105997 C T 74 GENIC heterozygous 506071841