chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 12606344 12606345 G A 37 INTERGENIC homozygous 798967201 7 12606416 12606417 T C 34 GENIC homozygous 798967202 7 12606957 12606958 G A 41 GENIC homozygous 798967203 7 12607017 12607018 T G 49 GENIC possibly homozygous 798967204 7 12607024 12607025 C T 48 GENIC possibly homozygous 798967205 7 12607316 12607317 A G 25 GENIC homozygous 798967206 7 12607356 12607357 G A 24 GENIC homozygous 798967207 7 12607357 12607358 C A 23 GENIC homozygous 798967208 7 12607420 12607421 C A 33 GENIC homozygous 798967209 7 12607854 12607855 T C 30 GENIC homozygous 798967210 7 12608442 12608443 G A 28 GENIC homozygous 798967211 7 12609374 12609375 G T 38 GENIC homozygous 798967212 7 12609394 12609395 C T 35 GENIC homozygous 798967213 7 12609440 12609441 C T 32 GENIC possibly homozygous 798967214 7 12609713 12609714 T C 39 INTERGENIC homozygous 798967215