chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 46326063 46326064 T TA 21 GENIC heterozygous 729729577 10 46326063 46326064 T TAA 21 GENIC possibly homozygous 729729578 10 46326318 46326319 G A 22 GENIC homozygous 601578223 10 46326461 46326462 C CAG 31 GENIC homozygous 729729579 10 46329717 46329718 G A 29 GENIC homozygous 601578224 10 46329790 46329791 A AGGTGGCTCAGC 21 GENIC homozygous 729729580 10 46329947 46329948 A - 23 GENIC homozygous 729729581 10 46330297 46330298 G T 20 GENIC homozygous 603489332 10 46332855 46332856 G A 34 GENIC homozygous 601578225 10 46332973 46332974 T G 35 GENIC homozygous 601578226 10 46333785 46333786 A G 17 GENIC homozygous 601578227 10 46334734 46334757 AGGATAGCCCACAGCAGGGCCAT ----------------------- 14 GENIC homozygous 729729582 10 46334793 46334794 T TTCACTCAC 12 GENIC homozygous 729729584 10 46335402 46335403 A ATG 7 GENIC heterozygous 729729585 10 46335402 46335403 A ATGTG 7 GENIC heterozygous 729729586 10 46335769 46335770 T C 14 GENIC homozygous 601578228 10 46336211 46336227 TCCGTCCGTCCGTCCG ---------------- 6 GENIC homozygous 729729588 10 46338748 46338749 T TACACAC 1 GENIC homozygous 729729593 10 46338903 46338904 C T 27 GENIC homozygous 601578229 10 46339489 46339490 A G 26 GENIC homozygous 601578230 10 46339805 46339806 A T 26 GENIC homozygous 601578231 10 46340825 46340826 C T 21 GENIC homozygous 603489333 10 46341435 46341436 T C 21 GENIC homozygous 601578232 10 46343272 46343273 G A 9 GENIC homozygous 601578233 10 46346409 46346410 T C 24 GENIC homozygous 603489334