chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 117091374 117091375 G C 29 GENIC homozygous 140688893 X 117091659 117091659 T 25 GENIC possibly homozygous 140594037 X 117091716 117091717 G A 25 GENIC homozygous 140688894 X 117092922 117092923 G A 11 GENIC possibly homozygous 140688895 X 117093887 117093887 AT 23 GENIC homozygous 140594038 X 117097541 117097549 GGGAATAG 8 GENIC heterozygous 147764740 X 117097620 117097621 A G 14 GENIC homozygous 145226201 X 117097950 117097951 A G 31 GENIC homozygous 140688896 X 117098699 117098700 C T 26 GENIC homozygous 140688897 X 117100030 117100031 C T 23 GENIC homozygous 140688898 X 117100253 117100254 C T 30 GENIC homozygous 140688899 X 117103528 117103529 G T 32 GENIC homozygous 140688900 X 117103543 117103544 C T 33 GENIC homozygous 140688901 X 117104047 117104048 A G 25 GENIC homozygous 140688902 X 117104336 117104337 T C 31 GENIC homozygous 140688903 X 117107365 117107366 G C 33 GENIC homozygous 140688904 X 117107480 117107481 C T 21 GENIC homozygous 140688905 X 117097570 117097571 G A 3 GENIC homozygous 141065700