chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 81607357 81607358 T C 25 GENIC homozygous 935424023 7 81607414 81607415 T C 33 GENIC homozygous 935424024 7 81607540 81607541 A G 36 GENIC homozygous 935424025 7 81607794 81607795 T G 30 GENIC homozygous 935424026 7 81608034 81608035 T A 29 GENIC homozygous 935424027 7 81608716 81608717 C G 17 GENIC homozygous 935424028 7 81608792 81608793 T C 18 GENIC homozygous 935424029 7 81609170 81609171 T C 36 GENIC homozygous 935424030 7 81609265 81609266 C T 26 GENIC possibly homozygous 935424031 7 81609907 81609908 T G 31 GENIC homozygous 935424032 7 81610149 81610150 T C 24 GENIC homozygous 935424033 7 81610214 81610215 G A 32 GENIC homozygous 935424034 7 81610336 81610337 G A 30 GENIC homozygous 935424035 7 81610409 81610410 T A 17 GENIC homozygous 935424036 7 81610779 81610780 A G 15 GENIC homozygous 935424037 7 81612166 81612167 A G 24 GENIC homozygous 935424038 7 81612548 81612549 A G 23 GENIC homozygous 935424039 7 81612690 81612691 A G 31 GENIC homozygous 935424040