chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 12606344 12606345 G A 25 INTERGENIC homozygous 790007824 7 12606416 12606417 T C 35 GENIC homozygous 790007825 7 12606947 12606948 A T 35 GENIC homozygous 790007826 7 12606957 12606958 G A 37 GENIC homozygous 790007827 7 12607017 12607018 T G 43 GENIC possibly homozygous 790007828 7 12607316 12607317 A G 36 GENIC homozygous 790007829 7 12607356 12607357 G A 30 GENIC homozygous 790007830 7 12607357 12607358 C A 30 GENIC homozygous 790007831 7 12607420 12607421 C A 49 GENIC homozygous 790007832 7 12607854 12607855 T C 43 GENIC homozygous 790007833 7 12608061 12608062 G C 41 GENIC homozygous 790007834 7 12608442 12608443 G A 29 GENIC homozygous 790007835 7 12609374 12609375 G T 30 GENIC homozygous 790007836 7 12609394 12609395 C T 29 GENIC homozygous 790007837 7 12609713 12609714 T C 40 INTERGENIC homozygous 790007838