chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 104720548 104720549 A G 11 GENIC homozygous 518638666 X 104721477 104721478 G A 7 GENIC homozygous 518638667 X 104723788 104723789 A G 9 GENIC homozygous 518638668 X 104724149 104724150 G T 7 GENIC heterozygous 518638669 X 104727044 104727045 A - 13 GENIC homozygous 690077792 X 104728161 104728162 G - 12 GENIC homozygous 690077793 X 104728227 104728228 C T 14 GENIC homozygous 518638670 X 104730133 104730134 T - 7 GENIC homozygous 690077795 X 104730149 104730150 T C 8 GENIC possibly homozygous 518638671 X 104731410 104731411 G T 13 GENIC heterozygous 518638672 X 104731568 104731569 C T 6 GENIC homozygous 518638673 X 104733371 104733372 G A 7 GENIC homozygous 518638674 X 104734161 104734162 G GC 8 GENIC possibly homozygous 690077796