chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 10058372 10058373 A G 33 GENIC homozygous 970774120 14 10058393 10058394 A C 34 GENIC homozygous 970774121 14 10058545 10058546 C A 32 GENIC homozygous 970774122 14 10058589 10058590 C T 35 GENIC homozygous 970774123 14 10058695 10058696 C T 26 GENIC homozygous 970774124 14 10058896 10058897 G A 36 GENIC homozygous 970774125 14 10059349 10059350 G A 26 GENIC homozygous 970774126 14 10060743 10060744 C T 32 GENIC homozygous 970774127 14 10060820 10060821 A G 46 GENIC homozygous 970774128 14 10060966 10060967 C T 27 GENIC homozygous 970774129 14 10061087 10061088 G C 36 GENIC homozygous 970774130 14 10061140 10061141 C T 26 GENIC homozygous 970774131 14 10061142 10061143 A T 26 GENIC homozygous 970774132 14 10061153 10061154 T C 26 GENIC homozygous 970774133 14 10061198 10061199 G A 27 GENIC homozygous 970774134 14 10061414 10061415 A C 17 GENIC homozygous 970774135 14 10061420 10061421 G A 17 GENIC homozygous 970774136 14 10061423 10061424 T A 18 GENIC homozygous 970774137 14 10061446 10061447 C A 17 GENIC homozygous 970774138 14 10061579 10061580 A G 36 GENIC homozygous 970774139 14 10061585 10061586 A G 38 GENIC homozygous 970774140 14 10061595 10061596 G A 37 GENIC homozygous 970774141 14 10061631 10061632 C T 29 GENIC homozygous 970774142 14 10061686 10061687 T C 17 GENIC homozygous 970774143 14 10061693 10061694 A G 19 GENIC homozygous 970774144 14 10061694 10061695 A G 19 GENIC homozygous 970774145 14 10061700 10061701 C T 22 GENIC homozygous 970774146 14 10061873 10061874 G A 29 GENIC homozygous 970774147 14 10061875 10061876 C A 29 GENIC homozygous 970774148