chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 101055537 101055538 G GCC 13 GENIC homozygous 55524181 6 101055554 101055556 GC -- 22 GENIC homozygous 55419821 6 101056135 101056136 C CTTT 5 GENIC heterozygous 55524183 6 101055958 101055962 ACAG ---- 16 GENIC homozygous 54601814 6 101056135 101056136 C CTTTT 5 GENIC heterozygous 54601815 6 101056561 101056562 A G 26 GENIC homozygous 54601818 6 101056889 101056890 T - 13 GENIC homozygous 54601820 6 101057505 101057506 G A 21 GENIC homozygous 54601821 6 101058413 101058414 A - 13 GENIC possibly homozygous 54601822 6 101058901 101058902 T G 12 GENIC homozygous 54601824 6 101058958 101058959 T TGAG 17 GENIC homozygous 54601825 6 101059518 101059519 A G 29 GENIC homozygous 54601826 6 101059884 101059885 A G 20 GENIC homozygous 54601827 6 101060936 101060937 C CT 10 GENIC heterozygous 54601828 6 101061249 101061250 G GT 9 GENIC heterozygous 55524187 6 101061380 101061381 G A 12 GENIC homozygous 54601830 6 101061885 101061891 TTTGTT ------ 1 GENIC homozygous 55524189 6 101062368 101062369 A AT 14 GENIC homozygous 54601831 6 101062423 101062435 GCACACCTCAGC ------------ 20 GENIC homozygous 54601832 6 101062947 101062948 T A 23 GENIC homozygous 54601833 6 101064349 101064350 T A 17 GENIC homozygous 54601834 6 101065477 101065478 T TACCTGAAAAA 18 GENIC homozygous 54601836 6 101066118 101066119 G GT 14 GENIC homozygous 54601837 6 101066831 101066832 A G 18 GENIC homozygous 54601838 6 101067142 101067143 C T 19 GENIC homozygous 54601839 6 101067165 101067166 G A 17 GENIC homozygous 54601840 6 101067168 101067169 G C 15 GENIC homozygous 54601841 6 101067169 101067170 G C 15 GENIC homozygous 54601842 6 101067296 101067297 A C 9 GENIC homozygous 54601846