chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 154270159 154270160 C T 20 GENIC homozygous 114060619 5 154270283 154270284 C T 16 GENIC homozygous 114060621 5 154271511 154271512 C G 30 GENIC homozygous 114060623 5 154271566 154271567 A G 32 GENIC homozygous 114060625 5 154271842 154271843 T C 25 GENIC homozygous 114060627 5 154273256 154273257 G A 16 GENIC homozygous 114060629 5 154273474 154273475 A G 11 GENIC homozygous 114060631 5 154273889 154273890 T A 30 GENIC homozygous 114060633 5 154274722 154274723 T C 18 GENIC possibly homozygous 114060635 5 154275661 154275662 A G 6 GENIC homozygous 114060637 5 154278101 154278102 G A 22 GENIC homozygous 114060639 5 154278337 154278338 C T 24 GENIC homozygous 114544055 5 154278524 154278525 C T 23 GENIC homozygous 114060641 5 154278653 154278654 G A 15 GENIC homozygous 114060643 5 154280138 154280139 G T 21 GENIC homozygous 114060645 5 154281458 154281459 T C 21 GENIC homozygous 114060647 5 154282121 154282122 T C 13 GENIC homozygous 114060649 5 154282915 154282916 A G 17 GENIC homozygous 114060651 5 154283316 154283317 A G 14 GENIC homozygous 114060653 5 154283551 154283552 G A 19 GENIC homozygous 114060655 5 154283567 154283568 G A 19 GENIC homozygous 114060657 5 154286039 154286040 A G 16 GENIC homozygous 114060659