chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 12606344 12606345 G A 38 INTERGENIC homozygous 807913501 7 12606416 12606417 T C 41 GENIC possibly homozygous 807913502 7 12606947 12606948 A T 42 GENIC possibly homozygous 807913503 7 12606957 12606958 G A 48 GENIC possibly homozygous 807913504 7 12607017 12607018 T G 50 GENIC heterozygous 807913505 7 12607024 12607025 C T 47 GENIC heterozygous 807913506 7 12607316 12607317 A G 37 GENIC homozygous 807913507 7 12607356 12607357 G A 28 GENIC homozygous 807913508 7 12607357 12607358 C A 28 GENIC homozygous 807913509 7 12607420 12607421 C A 42 GENIC possibly homozygous 807913510 7 12607854 12607855 T C 48 GENIC homozygous 807913511 7 12608061 12608062 G C 37 GENIC homozygous 807913512 7 12608442 12608443 G A 50 GENIC homozygous 807913513 7 12609240 12609241 C G 52 GENIC heterozygous 807913514 7 12609374 12609375 G T 36 GENIC possibly homozygous 807913515 7 12609394 12609395 C T 44 GENIC possibly homozygous 807913516 7 12609713 12609714 T C 46 INTERGENIC homozygous 807913517