chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 12606344 12606345 G A 30 INTERGENIC homozygous 803356777 7 12606416 12606417 T C 38 GENIC homozygous 803356778 7 12606957 12606958 G A 27 GENIC homozygous 803356779 7 12607017 12607018 T G 32 GENIC possibly homozygous 803356780 7 12607024 12607025 C T 31 GENIC possibly homozygous 803356781 7 12607316 12607317 A G 19 GENIC homozygous 803356782 7 12607356 12607357 G A 20 GENIC homozygous 803356783 7 12607357 12607358 C A 19 GENIC homozygous 803356784 7 12607420 12607421 C A 18 GENIC homozygous 803356785 7 12607854 12607855 T C 22 GENIC homozygous 803356786 7 12608442 12608443 G A 22 GENIC homozygous 803356787 7 12609374 12609375 G T 30 GENIC homozygous 803356788 7 12609394 12609395 C T 31 GENIC homozygous 803356789 7 12609440 12609441 C T 27 GENIC homozygous 803356790 7 12609713 12609714 T C 34 INTERGENIC homozygous 803356791