chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 157646292 157646293 T C 51 GENIC homozygous 137248762 4 157646546 157646547 A T 43 GENIC homozygous 137248763 4 157646792 157646793 G T 49 GENIC homozygous 137248764 4 157646855 157646856 G A 49 GENIC homozygous 137248765 4 157647329 157647330 A G 52 GENIC homozygous 137248766 4 157647658 157647659 G C 44 GENIC homozygous 137248767 4 157648999 157649000 C T 17 GENIC homozygous 137248768 4 157649488 157649489 T C 38 GENIC homozygous 137248769 4 157649932 157649933 G A 49 GENIC homozygous 137248770 4 157649978 157649979 A T 50 GENIC homozygous 137248771 4 157650336 157650337 A G 50 GENIC homozygous 137248772 4 157651004 157651005 G C 42 GENIC homozygous 137248773 4 157652973 157652974 G A 49 GENIC homozygous 137248774 4 157653090 157653091 C T 41 GENIC homozygous 137248775 4 157653319 157653320 T C 44 GENIC homozygous 137248776 4 157654967 157654968 G A 17 GENIC homozygous 137248777 4 157657502 157657503 T G 31 GENIC heterozygous 154221634 4 157657502 157657503 T 31 GENIC homozygous 403125165 4 157657489 157657489 TGA 31 GENIC homozygous 136925259 4 157653173 157653176 TCC 27 GENIC homozygous 136925258 4 157648901 157648901 GTTTTGTTTTGTTTTG 30 GENIC homozygous 136925256 4 157649696 157649696 G 37 GENIC homozygous 136925257 4 157654956 157654957 G A 18 GENIC homozygous 403125163 4 157654956 157654957 G 18 GENIC heterozygous 403125164 4 157657572 157657674 GCGCTTGCTAGGCAAGGGCTCTACCACTGAGCTAAATCCCCAACCCCGTTGATGTTGTTTTAAGGCAAGATCTCGGGGTTGGGGATTTAGCTCAGTGGTAGA 33 GENIC heterozygous 136925260 4 157658238 157658239 C T 44 GENIC homozygous 137248778 4 157658549 157658550 C A 45 GENIC possibly homozygous 137248779 4 157659133 157659134 G A 63 GENIC homozygous 137248780 4 157659834 157659835 A G 38 GENIC homozygous 137248781 4 157660727 157660735 TCTCTGTC 43 GENIC homozygous 136925261 4 157661632 157661633 A G 34 GENIC homozygous 137248782 4 157661730 157661731 C G 25 GENIC homozygous 137248783