chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6176768 6176769 A T 36 GENIC homozygous 980228171 14 6177149 6177150 T C 29 GENIC homozygous 980228172 14 6177400 6177401 G C 39 GENIC homozygous 980228173 14 6177456 6177457 T C 28 GENIC homozygous 980228174 14 6177559 6177560 A G 23 GENIC homozygous 980228175 14 6177626 6177627 A G 26 GENIC homozygous 980228176 14 6181139 6181140 G A 26 GENIC homozygous 980228177 14 6214864 6214865 C T 15 GENIC homozygous 980228178 14 6217368 6217369 C T 18 GENIC homozygous 980228179 14 6217845 6217846 C T 27 GENIC homozygous 980228180 14 6217987 6217988 C T 23 GENIC homozygous 980228181 14 6218260 6218261 A G 28 GENIC homozygous 980228182 14 6218882 6218883 C G 15 GENIC homozygous 980228183 14 6219313 6219314 C T 26 GENIC homozygous 980228184 14 6220214 6220215 C G 14 GENIC homozygous 980228185 14 6220714 6220715 A G 11 GENIC homozygous 980228186