chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 52775483 52775484 G T 20 GENIC homozygous 539580236 9 52776841 52776842 A G 20 GENIC homozygous 538333003 9 52778921 52778922 A - 10 GENIC homozygous 697603371 9 52778988 52778989 G C 15 GENIC homozygous 539580237 9 52779475 52779476 T C 25 GENIC possibly homozygous 538333004 9 52779690 52779691 A G 27 GENIC possibly homozygous 538333005 9 52779884 52779885 A G 20 GENIC homozygous 538333006 9 52780470 52780471 T - 17 GENIC homozygous 697603372 9 52780496 52780497 C T 21 GENIC homozygous 538333007 9 52780506 52780507 G GT 17 GENIC homozygous 697603373 9 52780926 52780927 A G 33 GENIC homozygous 538333008 9 52780940 52780941 A G 36 GENIC homozygous 538333009 9 52781023 52781024 C T 30 GENIC homozygous 538333010 9 52781073 52781074 T C 33 GENIC homozygous 538333011 9 52781165 52781166 G A 12 GENIC heterozygous 538333012 9 52782149 52782150 T C 18 GENIC homozygous 539580238 9 52782828 52782829 C T 22 GENIC homozygous 538333013 9 52783602 52783603 T C 35 GENIC homozygous 538333014 9 52783858 52783859 C CGGGGG 12 GENIC heterozygous 697603374 9 52784099 52784100 A G 21 GENIC homozygous 538333015