chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 60929070 60929071 A T 12 GENIC homozygous 554921346 2 60929086 60929087 T C 14 GENIC homozygous 554921347 2 60929211 60929212 T TTA 9 GENIC homozygous 702277436 2 60929265 60929266 T G 9 GENIC homozygous 554921348 2 60929886 60929887 T C 23 GENIC homozygous 553782490 2 60930547 60930548 A G 18 GENIC homozygous 553782491 2 60930719 60930720 G A 22 GENIC possibly homozygous 553782492 2 60930858 60930859 A G 10 GENIC homozygous 553782493 2 60931211 60931212 A T 22 GENIC homozygous 553782494 2 60931743 60931744 T A 25 GENIC homozygous 553782495 2 60931898 60931899 T C 18 GENIC homozygous 553782496 2 60932121 60932122 T A 25 GENIC homozygous 553782497 2 60932183 60932184 A G 24 GENIC homozygous 553782498 2 60932689 60932690 C T 17 GENIC homozygous 553782499 2 60932703 60932704 A G 21 GENIC homozygous 553782500 2 60933003 60933004 A AACACACACAC 5 GENIC homozygous 702277437 2 60933032 60933033 G A 10 GENIC homozygous 553782501 2 60933039 60933040 A AACACAC 9 GENIC homozygous 702277439 2 60933111 60933112 A C 15 GENIC homozygous 553782502 2 60933259 60933260 C T 32 GENIC homozygous 553782503