chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 41256042 41256043 T C 23 GENIC homozygous 115384906 12 41256093 41256094 T C 28 GENIC homozygous 115384908 12 41256134 41256135 A G 19 GENIC homozygous 115384910 12 41256162 41256163 G A 19 GENIC homozygous 115384912 12 41256447 41256448 G T 26 GENIC homozygous 115384914 12 41258311 41258312 A G 33 GENIC homozygous 115384916 12 41258500 41258501 T C 40 GENIC homozygous 115384918 12 41258567 41258568 A T 32 GENIC homozygous 115384920 12 41258919 41258920 G A 24 GENIC homozygous 115384922 12 41259287 41259288 C G 29 GENIC homozygous 115384924 12 41259321 41259322 T C 30 GENIC homozygous 115384926 12 41259411 41259412 C T 21 GENIC homozygous 115384928 12 41259651 41259652 G C 30 GENIC homozygous 115384930 12 41259655 41259656 A T 31 GENIC homozygous 115384932 12 41260653 41260654 A G 35 GENIC homozygous 115384934 12 41260753 41260754 G T 19 GENIC homozygous 115384936 12 41261017 41261018 C T 26 GENIC homozygous 115384942 12 41262598 41262599 C T 24 GENIC homozygous 115384944 12 41260935 41260936 T C 17 GENIC homozygous 115441920 12 41262681 41262682 G A 31 GENIC homozygous 115384946 12 41265639 41265640 C T 24 GENIC homozygous 115384952 12 41265750 41265751 C T 17 GENIC homozygous 115384954 12 41265751 41265752 C T 17 GENIC homozygous 115384956 12 41266337 41266338 G C 27 GENIC homozygous 115384958 12 41266394 41266395 C G 32 GENIC homozygous 115384960 12 41266409 41266410 C A 34 GENIC homozygous 115384962