chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 33876852 33876853 A G 20 GENIC homozygous 875112737 15 33877093 33877094 A G 16 GENIC homozygous 875112738 15 33877227 33877228 C A 20 GENIC homozygous 875112739 15 33877754 33877755 C T 16 GENIC homozygous 875112740 15 33877772 33877773 A C 13 GENIC homozygous 875112741 15 33877941 33877942 A C 22 GENIC homozygous 875112742 15 33878273 33878274 T C 16 GENIC homozygous 875112743 15 33878770 33878771 C T 8 GENIC heterozygous 875112744 15 33878870 33878871 T A 10 GENIC homozygous 875112745 15 33879117 33879118 A T 17 GENIC homozygous 875112746 15 33879592 33879593 C G 28 GENIC homozygous 875112747 15 33880630 33880631 A G 9 GENIC heterozygous 875112748 15 33881338 33881339 T C 8 GENIC homozygous 875112749 15 33881884 33881885 C T 25 GENIC homozygous 875112750 15 33882221 33882222 A G 17 GENIC homozygous 875112751 15 33882959 33882960 T C 23 GENIC homozygous 875112752 15 33885207 33885208 G A 15 GENIC homozygous 875112753 15 33887027 33887028 C T 26 GENIC homozygous 875112754 15 33887138 33887139 T C 27 GENIC homozygous 875112755 15 33887230 33887231 C T 20 GENIC homozygous 875112756 15 33887455 33887456 C G 22 GENIC homozygous 875112757 15 33887700 33887701 C T 9 GENIC homozygous 875112758 15 33887701 33887702 C T 9 GENIC homozygous 875112759 15 33888417 33888418 T C 20 GENIC homozygous 875112760 15 33889843 33889844 G A 10 GENIC homozygous 875112761 15 33890665 33890666 G A 12 GENIC heterozygous 875112762