chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 10058372 10058373 A G 29 GENIC homozygous 939199080 14 10058393 10058394 A C 22 GENIC homozygous 939199081 14 10058589 10058590 C T 27 GENIC homozygous 939199082 14 10058695 10058696 C T 28 GENIC homozygous 939199083 14 10058896 10058897 G A 23 GENIC homozygous 939199084 14 10059349 10059350 G A 17 GENIC homozygous 939199085 14 10060743 10060744 C T 23 GENIC homozygous 939199086 14 10060820 10060821 A G 36 GENIC homozygous 939199087 14 10060966 10060967 C T 24 GENIC homozygous 939199088 14 10061087 10061088 G C 28 GENIC homozygous 939199089 14 10061140 10061141 C T 19 GENIC homozygous 939199090 14 10061142 10061143 A T 19 GENIC homozygous 939199091 14 10061153 10061154 T C 17 GENIC homozygous 939199092 14 10061198 10061199 G A 21 GENIC homozygous 939199093 14 10061414 10061415 A C 29 GENIC homozygous 939199094 14 10061420 10061421 G A 27 GENIC homozygous 939199095 14 10061423 10061424 T A 27 GENIC homozygous 939199096 14 10061446 10061447 C A 26 GENIC homozygous 939199097 14 10061579 10061580 A G 24 GENIC homozygous 939199098 14 10061585 10061586 A G 27 GENIC homozygous 939199099 14 10061595 10061596 G A 30 GENIC homozygous 939199100 14 10061631 10061632 C T 25 GENIC homozygous 939199101 14 10061686 10061687 T C 30 GENIC homozygous 939199102 14 10061693 10061694 A G 28 GENIC homozygous 939199103 14 10061694 10061695 A G 28 GENIC homozygous 939199104 14 10061700 10061701 C T 28 GENIC homozygous 939199105 14 10061873 10061874 G A 25 GENIC homozygous 939199106 14 10061875 10061876 C A 24 GENIC homozygous 939199107