chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 104301940 104301941 T C 17 GENIC homozygous 117631212 9 104301945 104301946 G T 18 GENIC homozygous 117631214 9 104301950 104301951 A T 18 GENIC homozygous 117631218 9 104306598 104306599 T C 9 GENIC homozygous 120284184 9 104325467 104325468 G A 15 GENIC homozygous 117611825 9 104331612 104331613 G C 12 GENIC homozygous 117631414 9 104331838 104331839 C T 3 GENIC homozygous 117408890 9 104331840 104331841 C G 3 GENIC homozygous 117408892 9 104342694 104342695 A T 10 GENIC homozygous 117408916 9 104342699 104342700 G C 10 GENIC homozygous 117408918 9 104342719 104342720 A C 11 GENIC homozygous 117408919 9 104342721 104342722 A T 11 GENIC homozygous 117408921 9 104342744 104342745 C A 11 GENIC homozygous 117631436 9 104342693 104342694 G C 10 GENIC homozygous 117631434 9 104342755 104342756 G A 7 GENIC homozygous 117408927 9 104342765 104342766 C A 6 GENIC homozygous 117408929 9 104349015 104349016 T C 14 GENIC homozygous 117631452