chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 110304427 110304428 A G 51 GENIC homozygous 111672649 3 110304693 110304694 C T 45 GENIC possibly homozygous 111672651 3 110306725 110306726 A G 53 GENIC homozygous 111672652 3 110307794 110307795 T A 33 GENIC homozygous 111672654 3 110307945 110307946 C A 40 GENIC heterozygous 111672656 3 110308507 110308508 C T 37 GENIC homozygous 111672658 3 110308975 110308976 A G 37 GENIC homozygous 111672660 3 110310946 110310947 G C 54 GENIC possibly homozygous 111672661 3 110311445 110311446 A T 55 GENIC homozygous 111672663 3 110312415 110312416 C T 44 GENIC possibly homozygous 111672665 3 110312754 110312755 G A 35 GENIC homozygous 111672667 3 110312870 110312871 G A 43 GENIC possibly homozygous 111672668 3 110314044 110314045 C T 38 GENIC homozygous 111672670 3 110314630 110314631 G A 51 GENIC homozygous 111672672 3 110317183 110317184 A G 31 GENIC homozygous 111672674 3 110317206 110317207 T G 27 GENIC possibly homozygous 111672676 3 110317230 110317231 G A 35 GENIC heterozygous 111672678 3 110317260 110317261 A G 47 GENIC heterozygous 111672680 3 110317722 110317723 T A 44 GENIC heterozygous 111672682 3 110317784 110317785 C T 32 GENIC homozygous 111672684 3 110317964 110317965 G C 67 GENIC homozygous 111672686 3 110318079 110318080 C T 45 GENIC homozygous 111672688 3 110320626 110320627 G A 53 GENIC homozygous 111672690 3 110320719 110320720 T G 59 GENIC homozygous 111672691 3 110323714 110323715 T G 42 GENIC homozygous 111672693