chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 75250797 75250798 A G 29 GENIC homozygous 581580788 18 75251041 75251042 C - 24 GENIC homozygous 718813965 18 75251208 75251209 C T 29 GENIC homozygous 581580789 18 75251435 75251436 C A 15 GENIC homozygous 581580790 18 75251545 75251546 A ATCTCTCTC 6 GENIC homozygous 718813966 18 75251563 75251564 G C 16 GENIC homozygous 581580791 18 75252020 75252021 C A 22 GENIC homozygous 584451705 18 75252164 75252165 G T 42 GENIC homozygous 581580792 18 75252345 75252346 T C 36 GENIC homozygous 581580793 18 75252940 75252941 C T 31 GENIC homozygous 584451706 18 75253287 75253288 G A 30 GENIC homozygous 584451707 18 75253487 75253488 A T 28 GENIC homozygous 584451708 18 75253865 75253866 C CACAT 20 GENIC homozygous 718813968 18 75253873 75253874 T C 21 GENIC homozygous 584451709 18 75254068 75254069 C CG 12 GENIC homozygous 718813969 18 75254422 75254423 G C 45 GENIC homozygous 581580794 18 75254466 75254467 A G 40 GENIC homozygous 581580795 18 75254526 75254527 A C 35 GENIC homozygous 581580796 18 75254755 75254756 G A 23 GENIC homozygous 581580797 18 75254818 75254819 T TTTTC 8 GENIC homozygous 718813970 18 75254831 75254832 A C 10 GENIC homozygous 584451710 18 75254884 75254885 G A 12 GENIC homozygous 581580798 18 75255413 75255414 G A 55 GENIC homozygous 584451711 18 75255896 75255897 T G 40 GENIC homozygous 584451712 18 75255898 75255899 G GTGTGTGTATGTGTA 20 GENIC possibly homozygous 718813972 18 75255928 75255929 A ATG 40 GENIC homozygous 718813973 18 75255938 75255939 A ATGTG 38 GENIC homozygous 718813974 18 75255981 75255983 TG -- 19 GENIC possibly homozygous 718813975 18 75256104 75256105 C - 29 GENIC homozygous 718813977 18 75256129 75256130 G A 26 GENIC homozygous 584451713