chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 41315851 41315852 T C 38 GENIC heterozygous 925155158 10 41315874 41315875 A T 44 GENIC heterozygous 925155159 10 41315884 41315885 G A 55 GENIC heterozygous 925155160 10 41316825 41316826 C G 36 GENIC heterozygous 925155161 10 41316830 41316831 G - 37 GENIC heterozygous 925295806 10 41316833 41316834 T C 37 GENIC heterozygous 925155162 10 41316870 41316871 G - 53 GENIC heterozygous 925295807 10 41316880 41316881 T A 50 GENIC heterozygous 925155163 10 41316904 41316905 G A 37 GENIC heterozygous 925155164 10 41317117 41317118 G A 42 GENIC heterozygous 925155165 10 41317118 41317119 T G 45 GENIC heterozygous 925155166 10 41317137 41317138 T G 50 GENIC heterozygous 925155167 10 41317145 41317146 C T 50 GENIC heterozygous 925155168 10 41317147 41317148 G A 50 GENIC heterozygous 925155169 10 41317154 41317155 G T 54 GENIC heterozygous 925155170 10 41317157 41317158 A - 59 GENIC heterozygous 925295808 10 41317214 41317215 C T 59 GENIC heterozygous 925155171 10 41317215 41317216 C G 59 GENIC heterozygous 925155172