chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 12606344 12606345 G A 23 GENIC homozygous 941296364 7 12606416 12606417 T C 34 GENIC homozygous 941296365 7 12606947 12606948 A T 34 GENIC homozygous 941296366 7 12606957 12606958 G A 37 GENIC homozygous 941296367 7 12607017 12607018 T G 42 GENIC homozygous 941296368 7 12607024 12607025 C T 45 GENIC homozygous 941296369 7 12607316 12607317 A G 35 GENIC homozygous 941296370 7 12607356 12607357 G A 37 GENIC homozygous 941296371 7 12607357 12607358 C A 37 GENIC homozygous 941296372 7 12607420 12607421 C A 47 GENIC homozygous 941296373 7 12607854 12607855 T C 43 GENIC homozygous 941296374 7 12608061 12608062 G C 42 GENIC homozygous 941296375 7 12608442 12608443 G A 29 GENIC homozygous 941296376 7 12609374 12609375 G T 29 GENIC homozygous 941296377 7 12609394 12609395 C T 26 GENIC homozygous 941296378 7 12609713 12609714 T C 40 GENIC homozygous 941296379