chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 33176139 33176140 C T 24 GENIC homozygous 957916916 5 33176536 33176537 G T 3 GENIC heterozygous 957916917 5 33177051 33177052 A C 13 GENIC homozygous 957916918 5 33177272 33177273 C T 18 GENIC heterozygous 957916919 5 33177642 33177643 G A 27 GENIC heterozygous 957916920 5 33177668 33177669 C A 28 GENIC heterozygous 957916921 5 33177751 33177752 G T 34 GENIC heterozygous 957916922 5 33177776 33177777 T C 30 GENIC heterozygous 957916923 5 33177853 33177854 A G 19 GENIC heterozygous 957916924 5 33177994 33177995 G A 21 GENIC heterozygous 957916925 5 33178007 33178008 G A 19 GENIC heterozygous 957916926 5 33178076 33178077 C A 13 GENIC heterozygous 957916927 5 33178080 33178081 G A 13 GENIC heterozygous 957916928 5 33178083 33178084 G A 13 GENIC heterozygous 957916929 5 33178112 33178113 G A 11 GENIC heterozygous 957916930 5 33178678 33178679 G C 25 GENIC heterozygous 957916931 5 33178679 33178680 G T 25 GENIC heterozygous 957916932 5 33179644 33179645 A G 13 GENIC homozygous 957916933 5 33180034 33180035 C T 15 GENIC homozygous 957916934 5 33180442 33180443 C T 6 GENIC homozygous 957916935 5 33180660 33180661 T C 9 GENIC homozygous 957916936