chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 40073493 40073494 G T 23 GENIC homozygous 112485166 15 40073586 40073587 A G 20 GENIC homozygous 112851923 15 40073612 40073613 A C 20 GENIC homozygous 112851925 15 40073800 40073801 A G 36 GENIC homozygous 112485168 15 40073842 40073843 C G 32 GENIC homozygous 112672842 15 40109879 40109880 A C 17 GENIC homozygous 112672844 15 40116156 40116157 C A 33 GENIC homozygous 112485323 15 40116157 40116158 T C 32 GENIC homozygous 112485325 15 40116266 40116267 G A 30 GENIC homozygous 112485329 15 40145133 40145134 G C 3 GENIC homozygous 113097332 15 40192392 40192393 C G 26 GENIC homozygous 112672846 15 40192393 40192394 G C 27 GENIC homozygous 112672848 15 40230932 40230933 A G 21 GENIC homozygous 112485913 15 40230933 40230934 C A 21 GENIC homozygous 112485915 15 40230941 40230942 C A 20 GENIC homozygous 112485918 15 40353695 40353696 G C 8 GENIC homozygous 112486652 15 40353709 40353710 G A 8 GENIC homozygous 112486654 15 40414549 40414550 G T 26 GENIC homozygous 112486893 15 40414603 40414604 C A 36 GENIC homozygous 112486895 15 40418208 40418209 G C 9 GENIC homozygous 112808302 15 40451932 40451933 A G 23 GENIC homozygous 112808324 15 40451937 40451938 T C 21 GENIC homozygous 112808326 15 40451938 40451939 C G 21 GENIC homozygous 112808328