chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 46153291 46153292 T C 23 GENIC homozygous 116585152 10 46154242 46154243 T C 32 GENIC homozygous 116585154 10 46154293 46154294 G T 32 GENIC homozygous 116585156 10 46155084 46155085 A T 17 GENIC homozygous 116585160 10 46155183 46155184 G T 27 GENIC possibly homozygous 117312531 10 46156515 46156516 T C 32 GENIC homozygous 116585162 10 46157133 46157134 A C 32 GENIC homozygous 116585164 10 46157823 46157824 G T 41 GENIC homozygous 116585166 10 46157974 46157975 T G 19 GENIC homozygous 116585168 10 46158129 46158130 G T 15 GENIC possibly homozygous 118066553 10 46158123 46158124 A C 10 GENIC homozygous 117993461 10 46160188 46160189 T C 42 GENIC homozygous 116585170 10 46161086 46161087 G A 38 GENIC homozygous 116585172 10 46161134 46161135 A G 40 GENIC homozygous 116585174 10 46161538 46161539 T C 30 GENIC homozygous 116585176 10 46163104 46163105 C T 29 GENIC homozygous 116585178 10 46163192 46163193 A C 28 GENIC homozygous 116585180 10 46165911 46165912 G A 48 GENIC homozygous 116585182 10 46166013 46166014 G A 39 GENIC homozygous 116585184 10 46167646 46167647 A G 42 GENIC homozygous 116585186 10 46168488 46168489 G A 45 GENIC homozygous 116585188 10 46171455 46171456 A G 28 GENIC homozygous 116585190