chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6175387 6175388 A G 21 GENIC homozygous 956118007 14 6175388 6175389 G A 21 GENIC homozygous 956118008 14 6176768 6176769 A T 26 GENIC homozygous 956118009 14 6177149 6177150 T C 26 GENIC homozygous 956118010 14 6177400 6177401 G C 26 GENIC homozygous 956118011 14 6177456 6177457 T C 28 GENIC homozygous 956118012 14 6177559 6177560 A G 29 GENIC homozygous 956118013 14 6177626 6177627 A G 29 GENIC homozygous 956118014 14 6177826 6177827 A G 26 GENIC homozygous 956118015 14 6181139 6181140 G A 27 GENIC homozygous 956118016 14 6214864 6214865 C T 15 GENIC homozygous 956118017 14 6218929 6218930 C T 26 GENIC homozygous 956118018 14 6219311 6219312 C T 25 GENIC homozygous 956118019 14 6219445 6219446 G A 29 GENIC homozygous 956118020 14 6219600 6219601 G A 29 GENIC homozygous 956118021 14 6220214 6220215 C G 18 GENIC homozygous 956118022 14 6220223 6220224 C T 18 GENIC homozygous 956118023 14 6220406 6220407 G A 23 GENIC homozygous 956118024 14 6220714 6220715 A G 17 GENIC homozygous 956118025 14 6220981 6220982 A G 36 GENIC homozygous 956118026 14 6221230 6221231 T C 14 GENIC homozygous 956118027