chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 29808344 29808345 A G 11 GENIC homozygous 792091885 X 29808454 29808455 T C 13 GENIC homozygous 792091886 X 29810500 29810501 G A 7 GENIC homozygous 792091887 X 29810885 29810886 G A 9 GENIC homozygous 792091888 X 29811839 29811840 T C 14 GENIC possibly homozygous 792091889 X 29812573 29812574 G A 10 GENIC homozygous 792091890 X 29813611 29813612 C T 8 GENIC homozygous 792091891 X 29814185 29814186 G T 11 GENIC homozygous 792091892 X 29815656 29815657 A G 14 GENIC homozygous 792091893 X 29816718 29816719 T C 7 GENIC homozygous 792091894 X 29817224 29817225 T A 11 GENIC homozygous 792091895 X 29817426 29817427 C T 10 GENIC homozygous 792091896 X 29818470 29818471 G A 12 GENIC homozygous 792091897 X 29822149 29822150 G A 10 GENIC homozygous 792091898 X 29824030 29824031 C T 8 GENIC homozygous 792091899