chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 60929070 60929071 A T 16 GENIC homozygous 820836890 2 60929086 60929087 T C 16 GENIC homozygous 820836891 2 60929211 60929212 T TTA 18 GENIC heterozygous 820836892 2 60929265 60929266 T G 21 GENIC homozygous 820836893 2 60929886 60929887 T C 20 GENIC homozygous 820836894 2 60930547 60930548 A G 13 GENIC homozygous 820836895 2 60930719 60930720 G A 9 GENIC homozygous 820836896 2 60930858 60930859 A G 7 GENIC homozygous 820836897 2 60931211 60931212 A T 14 GENIC homozygous 820836898 2 60931743 60931744 T A 12 GENIC homozygous 820836899 2 60931898 60931899 T C 21 GENIC homozygous 820836900 2 60932121 60932122 T A 11 GENIC homozygous 820836901 2 60932183 60932184 A G 13 GENIC homozygous 820836902 2 60932689 60932690 C T 11 GENIC homozygous 820836903 2 60932703 60932704 A G 10 GENIC homozygous 820836904 2 60933111 60933112 A C 9 GENIC homozygous 820836905 2 60933259 60933260 C T 18 GENIC homozygous 820836906