chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 60929070 60929071 A T 20 GENIC homozygous 551526054 2 60929086 60929087 T C 17 GENIC homozygous 551526055 2 60929211 60929212 T TTA 15 GENIC possibly homozygous 700158819 2 60929265 60929266 T G 17 GENIC homozygous 551526056 2 60929886 60929887 T C 32 GENIC homozygous 550380490 2 60930547 60930548 A G 20 GENIC homozygous 550380491 2 60930719 60930720 G A 10 GENIC homozygous 550380492 2 60930858 60930859 A G 9 GENIC homozygous 550380493 2 60931211 60931212 A T 28 GENIC homozygous 550380494 2 60931743 60931744 T A 25 GENIC homozygous 550380495 2 60931898 60931899 T C 21 GENIC homozygous 550380496 2 60932121 60932122 T A 37 GENIC homozygous 550380497 2 60932183 60932184 A G 38 GENIC homozygous 550380498 2 60932689 60932690 C T 14 GENIC homozygous 550380499 2 60932703 60932704 A G 17 GENIC homozygous 550380500 2 60933003 60933004 A AACACACACAC 8 GENIC homozygous 700158820 2 60933032 60933033 G A 14 GENIC homozygous 550380501 2 60933039 60933040 A AACACAC 13 GENIC homozygous 700158822 2 60933111 60933112 A C 17 GENIC homozygous 550380502 2 60933259 60933260 C T 19 GENIC homozygous 550380503