chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 28459909 28459910 C T 11 GENIC homozygous 939861619 X 28460532 28460533 G A 17 GENIC homozygous 939861620 X 28460872 28460873 G A 6 GENIC homozygous 939861621 X 28461085 28461086 A G 6 GENIC homozygous 939861622 X 28462942 28462943 G A 9 GENIC homozygous 939861623 X 28464376 28464377 C T 15 GENIC homozygous 939861624 X 28464534 28464535 G A 6 GENIC homozygous 939861625 X 28465225 28465226 T C 14 GENIC homozygous 939861626 X 28465560 28465561 A G 11 GENIC homozygous 939861627 X 28465565 28465566 A G 10 GENIC homozygous 939861628 X 28467239 28467240 T A 8 GENIC homozygous 939861629 X 28467771 28467772 C A 7 GENIC homozygous 939861630 X 28468612 28468613 G A 12 GENIC homozygous 939861631 X 28468675 28468676 T G 5 GENIC homozygous 939861632 X 28469296 28469297 T G 9 GENIC homozygous 939861633 X 28469778 28469779 A T 3 GENIC homozygous 939861634 X 28470312 28470313 A G 13 GENIC homozygous 939861635 X 28470874 28470875 T A 7 GENIC homozygous 939861636 X 28471879 28471880 C G 16 GENIC homozygous 939861637 X 28472008 28472009 A G 21 GENIC homozygous 939861638 X 28472044 28472045 G A 23 GENIC homozygous 939861639 X 28472351 28472352 C G 17 GENIC homozygous 939861640