chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 30362532 30362533 C T 29 GENIC homozygous 140633057 X 30362885 30362886 T A 28 GENIC homozygous 140633058 X 30365818 30365819 A 18 GENIC homozygous 140580844 X 30366707 30366708 C T 17 GENIC homozygous 140633059 X 30368739 30368740 C A 18 GENIC homozygous 140633060 X 30368849 30368850 G C 16 GENIC homozygous 140633061 X 30369213 30369214 A T 18 GENIC homozygous 140633062 X 30369273 30369273 A 17 GENIC homozygous 140580845 X 30370441 30370442 C G 21 GENIC homozygous 140633063 X 30377750 30377753 ATC 11 GENIC heterozygous 140580846 X 30378438 30378439 C A 6 GENIC heterozygous 140633064 X 30379940 30379941 C T 16 GENIC homozygous 140633065 X 30380078 30380079 C T 27 GENIC homozygous 140633066 X 30381305 30381306 C T 26 GENIC homozygous 140633067 X 30385360 30385360 CA 15 GENIC homozygous 140580847 X 30386098 30386099 A G 30 GENIC possibly homozygous 140633068 X 30392348 30392349 T 13 GENIC homozygous 140580848