chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 46326063 46326064 T TAA 5 GENIC homozygous 703696854 10 46326318 46326319 G A 27 GENIC homozygous 557004495 10 46326461 46326462 C CAG 20 GENIC homozygous 703696855 10 46329717 46329718 G A 32 GENIC homozygous 557004496 10 46329790 46329791 A AGGTGGCTCAGC 24 GENIC homozygous 703696856 10 46329947 46329948 A - 13 GENIC homozygous 703696857 10 46330297 46330298 G T 33 GENIC homozygous 558756888 10 46332855 46332856 G A 22 GENIC homozygous 557004497 10 46332973 46332974 T G 30 GENIC homozygous 557004498 10 46333785 46333786 A G 21 GENIC homozygous 557004499 10 46334734 46334757 AGGATAGCCCACAGCAGGGCCAT ----------------------- 22 GENIC homozygous 703696858 10 46334793 46334794 T TTCACTCAC 23 GENIC homozygous 703696860 10 46335402 46335403 A ATGTG 13 GENIC heterozygous 703696862 10 46335402 46335403 A ATGTGTG 13 GENIC possibly homozygous 703696863 10 46335769 46335770 T C 32 GENIC homozygous 557004500 10 46336211 46336227 TCCGTCCGTCCGTCCG ---------------- 1 GENIC homozygous 703696864 10 46338748 46338749 T TACAC 6 GENIC heterozygous 703696868 10 46338748 46338749 T TACACAC 6 GENIC heterozygous 703696869 10 46338903 46338904 C T 31 GENIC homozygous 557004501 10 46339489 46339490 A G 16 GENIC homozygous 557004502 10 46339805 46339806 A T 36 GENIC homozygous 557004503 10 46340825 46340826 C T 39 GENIC homozygous 558756889 10 46341435 46341436 T C 28 GENIC homozygous 557004504 10 46343272 46343273 G A 23 GENIC homozygous 557004505 10 46346409 46346410 T C 22 GENIC homozygous 558756890