chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 264060117 264060118 A G 50 GENIC homozygous 928200055 1 264060592 264060593 C A 33 GENIC homozygous 928200056 1 264061466 264061467 T C 43 GENIC homozygous 928200057 1 264061991 264061992 G A 20 GENIC homozygous 928200058 1 264062033 264062034 T G 7 GENIC homozygous 928200059 1 264062097 264062098 T C 9 GENIC homozygous 928200060 1 264062098 264062099 C A 9 GENIC homozygous 928200061 1 264062297 264062298 T C 48 GENIC homozygous 928200062 1 264062381 264062382 C T 38 GENIC homozygous 928200063 1 264062501 264062502 A G 36 GENIC homozygous 928200064 1 264062858 264062859 G T 38 GENIC homozygous 928200065 1 264064003 264064004 A G 46 GENIC homozygous 928200066 1 264064234 264064235 T G 41 GENIC homozygous 928200067 1 264064641 264064642 C T 47 GENIC possibly homozygous 928200068 1 264064988 264064989 A G 51 GENIC homozygous 928200069 1 264067060 264067061 T C 47 GENIC homozygous 928200070 1 264067293 264067294 A G 35 GENIC homozygous 928200071 1 264068572 264068573 G A 36 GENIC homozygous 928200072 1 264070568 264070569 C T 45 GENIC homozygous 928200073 1 264071386 264071387 G A 36 GENIC homozygous 928200074