chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 228661637 228661638 T C 1 GENIC homozygous 591625013 1 228661888 228661889 G C 14 GENIC homozygous 591625014 1 228662170 228662171 G A 16 GENIC homozygous 591625015 1 228662393 228662394 C T 8 GENIC homozygous 591625016 1 228664212 228664213 G A 15 GENIC possibly homozygous 591625017 1 228665193 228665194 T C 4 GENIC homozygous 591625018 1 228666155 228666156 A G 4 GENIC homozygous 591625019 1 228669631 228669632 T C 1 GENIC homozygous 591625020 1 228670146 228670147 A G 6 GENIC homozygous 591625021 1 228671386 228671387 G A 4 GENIC homozygous 591625022 1 228673616 228673617 C T 2 GENIC homozygous 591625023 1 228675201 228675202 T C 16 GENIC possibly homozygous 591625024 1 228675312 228675313 C T 9 GENIC homozygous 591625025 1 228675817 228675819 CA -- 1 GENIC homozygous 723293516 1 228675822 228675825 GCC --- 1 GENIC homozygous 723293517 1 228676534 228676535 G T 6 GENIC homozygous 591625026 1 228678058 228678059 G A 4 GENIC homozygous 591625027 1 228678104 228678105 A G 1 GENIC homozygous 591625028 1 228678862 228678863 C A 5 GENIC heterozygous 591625029 1 228678931 228678932 A G 10 GENIC heterozygous 591625030 1 228680073 228680074 C T 9 GENIC homozygous 591625031 1 228681222 228681223 A T 12 GENIC possibly homozygous 591625032