chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 33876852 33876853 A G 30 INTERGENIC homozygous 795867723 15 33877093 33877094 A G 39 GENIC homozygous 795867724 15 33877227 33877228 C A 30 GENIC homozygous 795867725 15 33877754 33877755 C T 24 GENIC homozygous 795867726 15 33877772 33877773 A C 25 GENIC possibly homozygous 795867727 15 33877837 33877838 C G 26 GENIC homozygous 795867728 15 33877851 33877852 C T 29 GENIC homozygous 795867729 15 33877941 33877942 A C 28 GENIC homozygous 795867730 15 33878273 33878274 T C 39 GENIC homozygous 795867731 15 33878665 33878666 C G 28 GENIC heterozygous 795867732 15 33878770 33878771 C T 31 GENIC possibly homozygous 795867733 15 33878917 33878918 C T 42 GENIC heterozygous 795867734 15 33878926 33878927 T C 47 GENIC heterozygous 795867735 15 33878932 33878933 T C 60 GENIC heterozygous 795867736 15 33878938 33878939 A G 64 GENIC heterozygous 795867737 15 33879117 33879118 A T 22 GENIC homozygous 795867738 15 33879303 33879304 G T 23 GENIC homozygous 795867739 15 33879592 33879593 C G 34 GENIC homozygous 795867740 15 33880630 33880631 A G 31 GENIC homozygous 795867741 15 33881338 33881339 T C 16 GENIC homozygous 795867742 15 33881884 33881885 C T 30 GENIC homozygous 795867743 15 33882221 33882222 A G 23 GENIC homozygous 795867744 15 33882959 33882960 T C 41 GENIC homozygous 795867745 15 33885207 33885208 G A 42 GENIC possibly homozygous 795867746 15 33887027 33887028 C T 36 GENIC homozygous 795867747 15 33887138 33887139 T C 38 GENIC homozygous 795867748 15 33887230 33887231 C T 43 GENIC homozygous 795867749 15 33887455 33887456 C G 35 GENIC homozygous 795867750 15 33887700 33887701 C T 25 GENIC homozygous 795867751 15 33887701 33887702 C T 25 GENIC possibly homozygous 795867752 15 33888417 33888418 T C 35 GENIC homozygous 795867753 15 33889843 33889844 G A 37 GENIC homozygous 795867754 15 33890665 33890666 G A 56 GENIC heterozygous 795867755