chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 15992174 15992175 A C 26 GENIC homozygous 944821035 12 15994155 15994156 G A 19 GENIC homozygous 944821036 12 15994169 15994170 G A 19 GENIC homozygous 944821037 12 15994772 15994773 G A 35 GENIC homozygous 944821038 12 15995070 15995071 C T 27 GENIC homozygous 944821039 12 15995073 15995074 A G 25 GENIC homozygous 944821040 12 15995891 15995892 G T 23 GENIC homozygous 944821041 12 16004207 16004208 G T 26 GENIC homozygous 944821042 12 16005907 16005908 T C 20 GENIC homozygous 944821043 12 16007686 16007687 A C 27 GENIC homozygous 944821044 12 16009017 16009018 T C 26 GENIC homozygous 944821045 12 16009450 16009451 G A 23 GENIC homozygous 944821046 12 16010351 16010352 A C 38 GENIC homozygous 944821047 12 16010445 16010446 C T 28 GENIC homozygous 944821048 12 16010665 16010666 T C 25 GENIC homozygous 944821049 12 16011107 16011108 G A 22 GENIC homozygous 944821050