chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 79671036 79671037 A G 51 GENIC homozygous 117594052 9 79672760 79672760 TGTTC 33 GENIC homozygous 128726900 9 79673587 79673597 TCCCCGCTCA 6 GENIC homozygous 128726901 9 79673610 79673611 T 7 GENIC homozygous 128726902 9 79673615 79673615 A 7 GENIC homozygous 128726903 9 79673629 79673632 GGG 9 GENIC homozygous 128726904 9 79673636 79673637 G 9 GENIC homozygous 128726905 9 79673669 79673670 C 16 GENIC homozygous 128726906 9 79673676 79673678 TA 17 GENIC homozygous 128726907 9 79673680 79673682 CC 18 GENIC homozygous 128726908 9 79673691 79673691 C 19 GENIC homozygous 128726909 9 79673696 79673696 T 19 GENIC homozygous 128726910 9 79673708 79673708 T 22 GENIC homozygous 128726911 9 79673716 79673716 C 23 GENIC homozygous 128726912 9 79673667 79673668 A T 16 GENIC homozygous 117809024 9 79727428 79727429 G 27 GENIC homozygous 128726913 9 79727431 79727432 G 27 GENIC homozygous 128726914 9 79727497 79727498 A 17 GENIC homozygous 128726915 9 79727502 79727503 A 17 GENIC homozygous 128726916 9 79727508 79727509 G A 17 GENIC homozygous 117380750 9 79727512 79727513 T G 16 GENIC homozygous 117380751 9 79727538 79727539 C 14 GENIC homozygous 128726917 9 79727585 79727585 C 13 GENIC homozygous 128726918 9 79727602 79727603 C 15 GENIC homozygous 128726919 9 79727616 79727617 G T 17 GENIC homozygous 123203952 9 79727617 79727618 T G 17 GENIC homozygous 123203953 9 79727632 79727633 A T 19 GENIC homozygous 123203954 9 79727633 79727634 T A 19 GENIC homozygous 123203955 9 79727665 79727665 A 16 GENIC homozygous 128726920 9 79727667 79727668 G 16 GENIC homozygous 128726921 9 79727675 79727676 T A 18 GENIC homozygous 123203960 9 79727677 79727678 C 18 GENIC homozygous 128726922 9 79727690 79727691 G A 22 GENIC homozygous 117594054 9 79727691 79727692 A G 22 GENIC homozygous 123203962 9 79736688 79736689 C 31 GENIC homozygous 128726923 9 79736692 79736693 C 31 GENIC homozygous 128726924 9 79746560 79746561 C A 20 GENIC homozygous 128774622