chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 33876852 33876853 A G 83 INTERGENIC possibly homozygous 782369095 15 33877093 33877094 A G 50 GENIC homozygous 782369096 15 33877227 33877228 C A 68 GENIC homozygous 782369097 15 33877754 33877755 C T 33 GENIC homozygous 782369098 15 33877772 33877773 A C 36 GENIC homozygous 782369099 15 33877837 33877838 C G 37 GENIC homozygous 782369100 15 33877851 33877852 C T 44 GENIC homozygous 782369101 15 33877941 33877942 A C 55 GENIC homozygous 782369102 15 33878273 33878274 T C 49 GENIC homozygous 782369103 15 33878665 33878666 C G 38 GENIC heterozygous 782369104 15 33878770 33878771 C T 48 GENIC possibly homozygous 782369105 15 33879117 33879118 A T 56 GENIC homozygous 782369106 15 33879303 33879304 G T 56 GENIC possibly homozygous 782369107 15 33879592 33879593 C G 64 GENIC homozygous 782369108 15 33880630 33880631 A G 40 GENIC possibly homozygous 782369109 15 33881159 33881160 A T 74 GENIC homozygous 782369110 15 33881338 33881339 T C 38 GENIC homozygous 782369111 15 33881884 33881885 C T 50 GENIC homozygous 782369112 15 33882221 33882222 A G 57 GENIC homozygous 782369113 15 33882959 33882960 T C 66 GENIC homozygous 782369114 15 33885207 33885208 G A 41 GENIC homozygous 782369115 15 33887027 33887028 C T 59 GENIC homozygous 782369116 15 33887138 33887139 T C 66 GENIC homozygous 782369117 15 33887230 33887231 C T 60 GENIC homozygous 782369118 15 33887455 33887456 C G 58 GENIC homozygous 782369119 15 33887700 33887701 C T 49 GENIC possibly homozygous 782369120 15 33887701 33887702 C T 53 GENIC possibly homozygous 782369121 15 33888417 33888418 T C 44 GENIC homozygous 782369122 15 33889843 33889844 G A 61 GENIC homozygous 782369123 15 33890665 33890666 G A 92 GENIC heterozygous 782369124