chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 10058372 10058373 A G 36 GENIC homozygous 953285879 14 10058393 10058394 A C 31 GENIC homozygous 953285880 14 10058545 10058546 C A 32 GENIC homozygous 953285881 14 10058589 10058590 C T 33 GENIC homozygous 953285882 14 10058695 10058696 C T 38 GENIC homozygous 953285883 14 10058896 10058897 G A 29 GENIC homozygous 953285884 14 10059349 10059350 G A 27 GENIC homozygous 953285885 14 10060743 10060744 C T 21 GENIC homozygous 953285886 14 10060820 10060821 A G 22 GENIC homozygous 953285887 14 10060966 10060967 C T 25 GENIC homozygous 953285888 14 10061087 10061088 G C 20 GENIC homozygous 953285889 14 10061140 10061141 C T 17 GENIC homozygous 953285890 14 10061142 10061143 A T 17 GENIC homozygous 953285891 14 10061153 10061154 T C 18 GENIC homozygous 953285892 14 10061198 10061199 G A 22 GENIC homozygous 953285893 14 10061414 10061415 A C 26 GENIC homozygous 953285894 14 10061420 10061421 G A 26 GENIC homozygous 953285895 14 10061423 10061424 T A 26 GENIC homozygous 953285896 14 10061446 10061447 C A 27 GENIC homozygous 953285897 14 10061631 10061632 C T 36 GENIC homozygous 953285898 14 10061686 10061687 T C 30 GENIC homozygous 953285899 14 10061693 10061694 A G 30 GENIC homozygous 953285900 14 10061694 10061695 A G 30 GENIC homozygous 953285901 14 10061700 10061701 C T 32 GENIC homozygous 953285902 14 10061873 10061874 G A 29 GENIC homozygous 953285903 14 10061875 10061876 C A 27 GENIC homozygous 953285904