chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 243552164 243552165 T C 11 GENIC homozygous 946330685 2 243553214 243553215 A C 26 GENIC homozygous 946330686 2 243556902 243556903 T C 19 GENIC homozygous 946330687 2 243556961 243556962 C T 24 GENIC homozygous 946330688 2 243557344 243557345 T C 29 GENIC homozygous 946330689 2 243558108 243558109 C T 26 GENIC homozygous 946330690 2 243558213 243558214 C T 9 GENIC homozygous 946330691 2 243558339 243558340 G A 6 GENIC homozygous 946330692 2 243559231 243559232 C A 21 GENIC homozygous 946330693 2 243559290 243559291 T G 23 GENIC homozygous 946330694 2 243559985 243559986 C T 29 GENIC homozygous 946330695 2 243560134 243560135 T C 30 GENIC possibly homozygous 946330696 2 243560178 243560179 G T 29 GENIC homozygous 946330697 2 243560446 243560447 T G 27 GENIC homozygous 946330698 2 243560544 243560545 C A 18 GENIC homozygous 946330699 2 243560581 243560582 C T 18 GENIC homozygous 946330700 2 243560718 243560719 A G 14 GENIC homozygous 946330701 2 243561224 243561225 T C 22 GENIC homozygous 946330702 2 243561420 243561421 A G 31 GENIC homozygous 946330703