chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 4579874 4579875 A G 54 GENIC homozygous 109074755 20 4580274 4580275 G A 63 GENIC possibly homozygous 109074757 20 4581497 4581498 C G 28 GENIC homozygous 109074759 20 4581986 4581987 G A 51 GENIC possibly homozygous 109074761 20 4582119 4582120 C T 59 GENIC possibly homozygous 109074763 20 4582624 4582625 C T 45 GENIC homozygous 109233527 20 4582721 4582722 T A 51 GENIC possibly homozygous 109074765 20 4582830 4582831 G A 65 GENIC homozygous 109074767 20 4582956 4582957 G T 57 GENIC homozygous 109074769 20 4582995 4582996 G A 56 GENIC homozygous 109074771 20 4583257 4583258 C T 42 GENIC homozygous 109074773 20 4583468 4583469 C A 47 GENIC possibly homozygous 109074775 20 4583562 4583563 G T 48 GENIC homozygous 109074777 20 4585198 4585199 C T 40 GENIC possibly homozygous 109074779 20 4586338 4586339 G A 43 GENIC homozygous 109074781 20 4586535 4586536 T A 41 GENIC homozygous 109074783 20 4586543 4586544 C A 40 GENIC homozygous 109074785 20 4586625 4586626 C T 37 GENIC homozygous 109074787 20 4586724 4586725 A G 47 GENIC homozygous 109074789 20 4587063 4587064 C T 58 GENIC homozygous 109074791 20 4589025 4589026 G A 54 GENIC homozygous 109074793 20 4589169 4589170 C T 63 GENIC possibly homozygous 109074795 20 4589422 4589423 T C 43 GENIC possibly homozygous 109074797 20 4590695 4590696 C T 63 GENIC homozygous 109074799 20 4590872 4590873 G A 60 GENIC homozygous 109074801 20 4591230 4591231 C T 77 GENIC homozygous 109074803 20 4591376 4591377 A G 60 GENIC homozygous 109074805 20 4591505 4591506 T C 46 GENIC homozygous 109074807 20 4592078 4592079 G A 61 GENIC homozygous 109074809 20 4592272 4592273 G A 44 GENIC possibly homozygous 109074811 20 4592800 4592801 G A 37 GENIC homozygous 109074813