chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 48489135 48489136 T G 13 GENIC homozygous 109737362 2 48489346 48489347 C T 11 GENIC homozygous 109737364 2 48489924 48489925 T C 23 GENIC homozygous 109737366 2 48490164 48490165 T C 22 GENIC homozygous 109737368 2 48490665 48490666 G C 21 GENIC homozygous 109737370 2 48490857 48490858 A C 6 GENIC homozygous 109737372 2 48490860 48490861 A C 6 GENIC homozygous 109737374 2 48491396 48491397 G A 12 GENIC homozygous 109737376 2 48492202 48492203 A G 23 GENIC homozygous 109737378 2 48492639 48492640 T C 14 GENIC homozygous 109737380 2 48492898 48492899 G T 28 GENIC homozygous 109737382 2 48495138 48495139 C T 17 GENIC homozygous 109737384 2 48495652 48495653 A C 15 GENIC homozygous 109737386 2 48495856 48495857 G A 6 GENIC homozygous 109737388 2 48496613 48496614 G A 15 GENIC homozygous 109737390 2 48496728 48496729 G A 23 GENIC homozygous 109737392 2 48496732 48496733 C A 22 GENIC homozygous 109737394 2 48497318 48497319 T C 18 GENIC homozygous 109737396 2 48499706 48499707 G 7 GENIC homozygous 127619796 2 48497867 48497869 TT 10 GENIC homozygous 127619795 2 48495535 48495535 AAAAC 16 GENIC homozygous 127619793 2 48496455 48496455 T 9 GENIC homozygous 127619794 2 48499713 48499714 A C 7 GENIC homozygous 109737398 2 48499722 48499723 C 7 GENIC homozygous 127619797 2 48499746 48499747 T C 8 GENIC homozygous 109737400 2 48499783 48499784 C 9 GENIC homozygous 127619798