chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 60928831 60928832 A C 33 GENIC possibly homozygous 673328759 2 60929212 60929213 T TATTA 18 GENIC possibly homozygous 770138871 2 60929886 60929887 T C 26 GENIC homozygous 673328760 2 60930439 60930440 G T 33 GENIC homozygous 673328761 2 60930547 60930548 A G 37 GENIC homozygous 673328762 2 60930858 60930859 A G 14 GENIC homozygous 673328763 2 60931163 60931164 T G 20 GENIC possibly homozygous 673328764 2 60931211 60931212 A T 28 GENIC homozygous 673328765 2 60931414 60931415 T G 37 GENIC possibly homozygous 673328766 2 60931693 60931694 A G 24 GENIC homozygous 673328767 2 60931721 60931722 A T 25 GENIC homozygous 673328768 2 60931743 60931744 T A 21 GENIC homozygous 673328769 2 60931898 60931899 T C 25 GENIC homozygous 673328770 2 60932965 60932966 T C 18 GENIC possibly homozygous 673328771 2 60933003 60933004 A AACACACACAC 3 GENIC homozygous 770138872 2 60933032 60933033 G A 3 GENIC homozygous 673328772 2 60933039 60933040 A AACACAC 2 GENIC homozygous 770138874 2 60933111 60933112 A C 17 GENIC homozygous 673328773 2 60933259 60933260 C T 24 GENIC homozygous 673328774