chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 105293208 105293209 A G 12 GENIC homozygous 981026312 X 105293287 105293288 A T 11 GENIC homozygous 981026313 X 105295440 105295441 G A 9 GENIC homozygous 981026314 X 105296887 105296888 T A 4 GENIC homozygous 981026315 X 105297118 105297119 C T 7 GENIC homozygous 981026316 X 105297905 105297906 T A 9 GENIC homozygous 981026317 X 105298659 105298660 A C 7 GENIC homozygous 981026318 X 105302163 105302164 C A 16 GENIC homozygous 981026319 X 105302184 105302185 T C 15 GENIC homozygous 981026320 X 105302210 105302211 C A 10 GENIC homozygous 981026321 X 105302256 105302257 G C 6 GENIC homozygous 981026322 X 105303025 105303026 T G 8 GENIC homozygous 981026323 X 105303915 105303916 A G 13 GENIC homozygous 981026324 X 105308529 105308530 A G 27 GENIC homozygous 981026325