chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 10005375 10005376 G A 40 GENIC homozygous 117243934 9 10006301 10006302 G A 46 GENIC homozygous 117243936 9 10007885 10007886 T C 52 GENIC homozygous 117243937 9 10009859 10009860 C T 32 GENIC homozygous 117243938 9 10009862 10009863 C T 29 GENIC homozygous 117243939 9 10009865 10009866 C T 29 GENIC homozygous 117243940 9 10009886 10009887 C 22 GENIC heterozygous 133491349 9 10010052 10010053 C A 39 GENIC homozygous 117243942 9 10010111 10010112 G T 39 GENIC homozygous 123119234 9 10010121 10010122 C G 38 GENIC homozygous 117243943 9 10010123 10010124 C T 37 GENIC homozygous 117243944 9 10010129 10010130 C G 40 GENIC homozygous 117243945 9 10010131 10010132 C G 40 GENIC homozygous 117243946 9 10010134 10010135 C A 41 GENIC homozygous 117243947 9 10010141 10010142 C A 41 GENIC homozygous 117243948 9 10010162 10010163 C G 43 GENIC homozygous 117243949 9 10010178 10010179 C G 44 GENIC homozygous 117243950 9 10010193 10010194 C G 42 GENIC homozygous 117243951 9 10012245 10012246 A C 50 GENIC homozygous 117243952 9 10010173 10010174 C T 44 GENIC homozygous 120424220 9 10009986 10009986 G 23 GENIC heterozygous 133563030 9 10009987 10009987 G 23 GENIC possibly homozygous 128678563 9 10010055 10010055 C 40 GENIC homozygous 128678564 9 10010077 10010077 T 43 GENIC homozygous 128678565 9 10010097 10010097 T 42 GENIC homozygous 128678566 9 10010105 10010105 T 39 GENIC homozygous 128678567 9 10010112 10010113 T G 37 GENIC homozygous 120405983 9 10010171 10010172 A T 41 GENIC homozygous 120405984 9 10010172 10010173 C A 44 GENIC homozygous 120424219