chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 95096903 95096904 T C 51 GENIC homozygous 137852131 6 95097117 95097118 T G 46 GENIC homozygous 137852132 6 95097246 95097246 GG 16 GENIC homozygous 137698417 6 95101149 95101150 T 21 GENIC homozygous 144749346 6 95101178 95101179 A 31 GENIC homozygous 144749347 6 95101183 95101185 AA 31 GENIC homozygous 144749348 6 95101870 95101871 A G 50 GENIC homozygous 137852134 6 95102244 95102245 A T 53 GENIC homozygous 137852135 6 95102634 95102634 A 43 GENIC possibly homozygous 137698420 6 95103516 95103517 T C 55 GENIC homozygous 137852137 6 95103995 95103996 G A 47 GENIC homozygous 137852138 6 95107188 95107189 A G 31 GENIC homozygous 137852139 6 95107310 95107311 A G 42 GENIC homozygous 137852140 6 95111880 95111881 T 21 GENIC homozygous 144749349 6 95113817 95113818 G C 55 GENIC homozygous 137852142 6 95116192 95116193 A T 44 GENIC homozygous 137852143 6 95116972 95116973 G T 35 GENIC homozygous 137852144 6 95118222 95118223 T 41 GENIC homozygous 137698423 6 95120038 95120038 A 47 GENIC possibly homozygous 137698424 6 95122437 95122470 CACACATCACCTCAGGCCTCTGGTACACTAGCG 5 GENIC homozygous 137698425 6 95122673 95122674 C T 48 GENIC possibly homozygous 137852150 6 95118623 95118624 A G 53 GENIC homozygous 137852145 6 95119978 95119979 C A 55 GENIC homozygous 137852146 6 95120861 95120862 T G 66 GENIC homozygous 137852147 6 95121382 95121383 G A 30 GENIC homozygous 137852148 6 95122654 95122655 T C 41 GENIC possibly homozygous 137852149 6 95101157 95101158 T A 16 GENIC homozygous 145593749 6 95102839 95102840 C T 55 GENIC homozygous 144769870 6 95109036 95109037 C T 3 GENIC homozygous 144769871 6 95115909 95115910 G C 47 GENIC homozygous 144769872