chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 19463441 19463442 T C 15 GENIC homozygous 140619416 X 19464219 19464220 A 4 GENIC homozygous 140578036 X 19464447 19464448 T C 11 GENIC homozygous 140619417 X 19465806 19465807 G C 8 GENIC homozygous 140619418 X 19469810 19469811 T C 9 GENIC homozygous 140619419 X 19470707 19470713 CTATAA 10 GENIC homozygous 140578037 X 19472188 19472189 A 10 GENIC homozygous 140578038 X 19473783 19473784 G A 11 GENIC homozygous 140619420 X 19474656 19474657 A G 12 GENIC homozygous 140619421 X 19475693 19475694 T C 6 GENIC homozygous 140619422 X 19475944 19475944 A 6 GENIC heterozygous 140578040 X 19475957 19475958 A 6 GENIC homozygous 140578041 X 19476135 19476136 G C 4 GENIC homozygous 140619423 X 19476785 19476786 T C 9 GENIC homozygous 140619424 X 19477198 19477199 A 10 GENIC homozygous 140578042 X 19477892 19477893 T C 13 GENIC homozygous 140619425 X 19479769 19479770 C T 10 GENIC homozygous 140619426 X 19480079 19480080 G A 8 GENIC homozygous 140619427 X 19482304 19482305 G A 8 GENIC homozygous 140619428 X 19483235 19483236 A G 11 GENIC homozygous 140619429 X 19484690 19484691 T A 7 GENIC homozygous 140619430 X 19484691 19484692 T A 7 GENIC homozygous 140619431 X 19484707 19484708 A C 7 GENIC homozygous 140619432 X 19485287 19485288 A G 8 GENIC homozygous 140619433 X 19486093 19486094 C T 5 GENIC homozygous 140619434