chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 30301466 30301467 G A 42 GENIC possibly homozygous 799969635 12 30301628 30301629 G A 22 GENIC homozygous 799969636 12 30301835 30301836 A T 32 GENIC homozygous 799969637 12 30302623 30302624 T C 64 GENIC homozygous 799969638 12 30302735 30302736 A G 24 GENIC heterozygous 799969639 12 30302751 30302752 A G 18 GENIC heterozygous 799969640 12 30303296 30303297 T C 3 GENIC homozygous 799969641 12 30303299 30303300 G A 3 GENIC homozygous 799969642 12 30303308 30303309 G T 5 GENIC homozygous 799969643 12 30303313 30303314 T A 7 GENIC homozygous 799969644 12 30303315 30303316 G A 8 GENIC homozygous 799969645 12 30303466 30303467 A G 39 GENIC homozygous 799969646 12 30303489 30303490 T G 37 GENIC homozygous 799969647 12 30303551 30303552 G A 20 GENIC homozygous 799969648 12 30303695 30303696 C T 30 GENIC homozygous 799969649