chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 46153326 46153327 C T 44 GENIC homozygous 117252569 10 46153570 46153571 G C 45 GENIC homozygous 116772312 10 46154242 46154243 T C 49 GENIC homozygous 116585154 10 46155131 46155132 C G 12 GENIC homozygous 133681298 10 46155133 46155134 T G 13 GENIC homozygous 133681299 10 46155135 46155136 C G 13 GENIC homozygous 133681300 10 46155137 46155138 C G 13 GENIC homozygous 133681301 10 46155139 46155140 C G 13 GENIC homozygous 133681302 10 46155141 46155142 A G 14 GENIC homozygous 133681303 10 46156515 46156516 T C 53 GENIC homozygous 116585162 10 46156525 46156526 G A 55 GENIC homozygous 116772314 10 46157133 46157134 A C 51 GENIC homozygous 116585164 10 46160188 46160189 T C 46 GENIC homozygous 116585170 10 46161538 46161539 T C 57 GENIC homozygous 116585176 10 46163170 46163171 G A 56 GENIC homozygous 117252571 10 46163192 46163193 A C 64 GENIC homozygous 116585180 10 46165788 46165789 C T 50 GENIC homozygous 116772316 10 46162515 46162527 GCCAGCAGTCTG 36 GENIC homozygous 133680122 10 46167646 46167647 A G 40 GENIC homozygous 116585186 10 46167794 46167803 AACAACAAC 50 GENIC homozygous 133680123 10 46171455 46171456 A G 48 GENIC homozygous 116585190