chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 60929070 60929071 A T 17 GENIC homozygous 658841781 2 60929086 60929087 T C 22 GENIC homozygous 658841782 2 60929211 60929212 T TTA 9 GENIC homozygous 762361598 2 60929265 60929266 T G 18 GENIC homozygous 658841783 2 60929886 60929887 T C 40 GENIC homozygous 658841784 2 60930547 60930548 A G 21 GENIC homozygous 658841785 2 60930719 60930720 G A 30 GENIC homozygous 658841786 2 60930858 60930859 A G 11 GENIC homozygous 658841787 2 60931211 60931212 A T 26 GENIC homozygous 658841788 2 60931743 60931744 T A 34 GENIC homozygous 658841789 2 60931898 60931899 T C 35 GENIC homozygous 658841790 2 60932121 60932122 T A 40 GENIC homozygous 658841791 2 60932183 60932184 A G 28 GENIC homozygous 658841792 2 60932689 60932690 C T 20 GENIC homozygous 658841793 2 60932703 60932704 A G 18 GENIC homozygous 658841794 2 60933003 60933004 A AACACACACAC 7 GENIC homozygous 762361599 2 60933032 60933033 G A 14 GENIC possibly homozygous 658841795 2 60933039 60933040 A AACACAC 13 GENIC heterozygous 762361601 2 60933111 60933112 A C 24 GENIC homozygous 658841796 2 60933259 60933260 C T 18 GENIC homozygous 658841797