chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 100658047 100658048 T C 24 GENIC homozygous 893514963 9 100658933 100658934 G A 16 GENIC heterozygous 893514964 9 100665730 100665731 C T 4 GENIC homozygous 893514965 9 100667501 100667502 T C 11 GENIC homozygous 893514966 9 100667992 100667993 A T 11 GENIC homozygous 893514967 9 100672458 100672459 T C 3 GENIC heterozygous 893514968 9 100673568 100673569 G A 15 GENIC homozygous 893514969 9 100674211 100674212 G C 15 GENIC homozygous 893514970 9 100676035 100676036 C T 5 GENIC heterozygous 893514971 9 100677728 100677729 G A 13 GENIC homozygous 893514972 9 100679844 100679845 T A 15 GENIC homozygous 893514973 9 100681792 100681793 A G 13 GENIC homozygous 893514974 9 100685355 100685356 G C 9 GENIC homozygous 893514975 9 100686084 100686085 G A 16 GENIC homozygous 893514976 9 100686335 100686336 C G 12 GENIC homozygous 893514977 9 100686595 100686596 A T 8 GENIC homozygous 893514978 9 100686596 100686597 A G 7 GENIC homozygous 893514979 9 100686639 100686640 G C 17 GENIC homozygous 893514980 9 100686787 100686788 T A 26 GENIC homozygous 893514981 9 100687497 100687498 T C 6 GENIC homozygous 893514982 9 100688580 100688581 G A 18 GENIC homozygous 893514983 9 100690317 100690318 T G 13 GENIC heterozygous 893514984 9 100696358 100696359 A G 26 GENIC homozygous 893514985 9 100696672 100696673 C T 11 GENIC homozygous 893514986 9 100697992 100697993 G A 17 GENIC homozygous 893514987 9 100698931 100698932 A T 6 GENIC heterozygous 893514988 9 100699264 100699265 T C 12 GENIC homozygous 893514989