chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 105292933 105292934 T A 13 GENIC homozygous 968507206 X 105293208 105293209 A G 19 GENIC homozygous 968507207 X 105293287 105293288 A T 14 GENIC homozygous 968507208 X 105296321 105296322 G A 22 GENIC homozygous 968507209 X 105296887 105296888 T A 15 GENIC homozygous 968507210 X 105297118 105297119 C T 20 GENIC homozygous 968507211 X 105297905 105297906 T A 20 GENIC possibly homozygous 968507212 X 105299521 105299522 C T 18 GENIC homozygous 968507213 X 105302163 105302164 C A 26 GENIC homozygous 968507214 X 105302184 105302185 T C 25 GENIC homozygous 968507215 X 105302210 105302211 C A 21 GENIC homozygous 968507216 X 105303568 105303569 C T 14 GENIC homozygous 968507217 X 105303915 105303916 A G 3 GENIC homozygous 968507218 X 105307953 105307954 G A 9 GENIC homozygous 968507219