chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 4578221 4578222 C T 19 GENIC homozygous 109233522 20 4578709 4578710 C A 40 GENIC homozygous 109233523 20 4579874 4579875 A G 19 GENIC homozygous 109074755 20 4579999 4580000 C T 14 GENIC homozygous 109233524 20 4581435 4581436 C T 18 GENIC homozygous 109233525 20 4581789 4581790 C T 39 GENIC homozygous 109233526 20 4582624 4582625 C T 22 GENIC homozygous 109233527 20 4582830 4582831 G A 31 GENIC homozygous 109074767 20 4582909 4582910 T A 33 GENIC homozygous 109233528 20 4582956 4582957 G T 28 GENIC homozygous 109074769 20 4582995 4582996 G A 31 GENIC homozygous 109074771 20 4583048 4583049 C T 33 GENIC homozygous 109233529 20 4583260 4583261 T C 36 GENIC homozygous 109233530 20 4583562 4583563 G T 26 GENIC homozygous 109074777 20 4584680 4584681 C T 26 GENIC homozygous 109233531 20 4585198 4585199 C T 10 GENIC homozygous 109074779 20 4585477 4585478 G C 35 GENIC homozygous 109233532 20 4585704 4585705 C T 35 GENIC homozygous 109233533 20 4586338 4586339 G A 10 GENIC homozygous 109074781 20 4586535 4586536 T A 29 GENIC homozygous 109074783 20 4586724 4586725 A G 20 GENIC homozygous 109074789 20 4587063 4587064 C T 21 GENIC homozygous 109074791 20 4587515 4587516 G A 34 GENIC homozygous 109233534 20 4589025 4589026 G A 26 GENIC homozygous 109074793 20 4589169 4589170 C T 30 GENIC homozygous 109074795 20 4589422 4589423 T C 12 GENIC homozygous 109074797 20 4590433 4590434 G A 19 GENIC homozygous 109233535 20 4590695 4590696 C T 27 GENIC homozygous 109074799 20 4590872 4590873 G A 40 GENIC homozygous 109074801 20 4591230 4591231 C T 19 GENIC homozygous 109074803 20 4591376 4591377 A G 28 GENIC homozygous 109074805 20 4591505 4591506 T C 18 GENIC homozygous 109074807 20 4591536 4591537 G A 24 GENIC homozygous 109233536 20 4591755 4591756 G A 37 GENIC homozygous 109233537