chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 60928831 60928832 A C 8 GENIC homozygous 590139628 2 60929212 60929213 T TATTA 2 GENIC homozygous 723655710 2 60929886 60929887 T C 11 GENIC homozygous 590139629 2 60930439 60930440 G T 13 GENIC possibly homozygous 590139630 2 60930547 60930548 A G 20 GENIC possibly homozygous 590139631 2 60931163 60931164 T G 13 GENIC possibly homozygous 590139632 2 60931211 60931212 A T 14 GENIC possibly homozygous 590139633 2 60931414 60931415 T G 20 GENIC possibly homozygous 590139634 2 60931693 60931694 A G 11 GENIC possibly homozygous 590139635 2 60931721 60931722 A T 14 GENIC homozygous 590139636 2 60931743 60931744 T A 10 GENIC possibly homozygous 590139637 2 60931898 60931899 T C 12 GENIC homozygous 590139638 2 60932965 60932966 T C 17 GENIC possibly homozygous 590139639 2 60933003 60933004 A AACACACACAC 1 GENIC homozygous 723655711 2 60933032 60933033 G A 1 GENIC homozygous 590139640 2 60933111 60933112 A C 9 GENIC possibly homozygous 590139641 2 60933259 60933260 C T 17 GENIC homozygous 590139642