chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 60929070 60929071 A T 25 GENIC homozygous 608313097 2 60929086 60929087 T C 26 GENIC homozygous 608313098 2 60929211 60929212 T TTA 26 GENIC possibly homozygous 732617016 2 60929265 60929266 T G 21 GENIC homozygous 608313099 2 60929886 60929887 T C 15 GENIC homozygous 607060122 2 60930547 60930548 A G 27 GENIC homozygous 607060123 2 60930719 60930720 G A 24 GENIC homozygous 607060124 2 60930858 60930859 A G 12 GENIC homozygous 607060125 2 60931211 60931212 A T 29 GENIC homozygous 607060126 2 60931743 60931744 T A 22 GENIC homozygous 607060127 2 60931898 60931899 T C 23 GENIC homozygous 607060128 2 60932121 60932122 T A 18 GENIC homozygous 607060129 2 60932183 60932184 A G 26 GENIC homozygous 607060130 2 60932689 60932690 C T 29 GENIC homozygous 607060131 2 60932703 60932704 A G 24 GENIC homozygous 607060132 2 60933003 60933004 A AACACACACAC 13 GENIC homozygous 732617017 2 60933032 60933033 G A 16 GENIC homozygous 607060133 2 60933039 60933040 A AACACAC 13 GENIC homozygous 732617019 2 60933111 60933112 A C 22 GENIC homozygous 607060134 2 60933259 60933260 C T 32 GENIC homozygous 607060135