chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 38105003 38105004 C T 36 GENIC heterozygous 817817952 8 38105020 38105021 A T 33 GENIC heterozygous 817817953 8 38105063 38105064 A G 30 GENIC heterozygous 817817954 8 38105069 38105070 T A 29 GENIC heterozygous 817817955 8 38105095 38105096 C T 29 GENIC heterozygous 817817956 8 38105105 38105106 T C 27 GENIC heterozygous 817817957 8 38105109 38105110 A C 30 GENIC heterozygous 817817958 8 38105173 38105174 G A 22 GENIC heterozygous 817817959 8 38105372 38105373 T C 35 GENIC heterozygous 817817960 8 38105377 38105378 A G 31 GENIC heterozygous 817817961 8 38105389 38105390 T C 37 GENIC heterozygous 817817962 8 38105479 38105480 G A 41 GENIC heterozygous 817817963 8 38105697 38105698 G C 25 GENIC heterozygous 817817964 8 38105751 38105752 A C 27 GENIC heterozygous 817817965 8 38105753 38105754 T G 25 GENIC heterozygous 817817966 8 38105759 38105760 A G 24 GENIC heterozygous 817817967 8 38105788 38105789 C T 28 GENIC heterozygous 817817968 8 38105981 38105982 C T 22 GENIC heterozygous 817817969 8 38105996 38105997 C T 23 GENIC heterozygous 817817970 8 38106005 38106006 G GGGA 23 GENIC heterozygous 817817971 8 38106008 38106010 AT -- 24 GENIC heterozygous 817817972