chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 82503909 82503910 T A 16 GENIC homozygous 515565934 5 82504006 82504007 A - 7 GENIC homozygous 689063878 5 82504131 82504132 C T 17 GENIC homozygous 515565935 5 82504564 82504565 A AG 14 GENIC homozygous 689063879 5 82504641 82504642 G GA 9 GENIC homozygous 689063880 5 82505279 82505280 C CT 9 GENIC homozygous 689063881 5 82505729 82505730 T TCC 26 GENIC heterozygous 689063882 5 82505731 82505732 T C 29 GENIC heterozygous 515565936 5 82505955 82505956 C T 35 GENIC homozygous 515565937 5 82506025 82506026 C T 28 GENIC homozygous 515565938 5 82506637 82506638 T C 33 GENIC homozygous 515565939 5 82507765 82507766 T C 16 GENIC homozygous 515565940 5 82508073 82508074 A C 10 GENIC homozygous 517612484 5 82508078 82508084 CTCTCT ------ 8 GENIC homozygous 689063883 5 82508605 82508607 TC -- 30 GENIC homozygous 689063884 5 82508623 82508624 C CTGTG 26 GENIC homozygous 689063885 5 82508751 82508757 GTGTGT ------ 17 GENIC possibly homozygous 689063886 5 82508872 82508873 G A 29 GENIC homozygous 517612485 5 82508951 82508952 T TTG 21 GENIC homozygous 689063888 5 82508979 82508980 T C 16 GENIC homozygous 515565941 5 82509247 82509248 T C 21 GENIC homozygous 515565942 5 82509429 82509430 G T 31 GENIC homozygous 515565943 5 82509473 82509474 C A 35 GENIC homozygous 515565944 5 82509938 82509939 C - 12 GENIC heterozygous 689063889