chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 29573965 29573966 G A 15 GENIC homozygous 960887800 5 29575301 29575302 G A 24 GENIC homozygous 960887801 5 29575895 29575896 C T 19 GENIC homozygous 960887802 5 29575911 29575912 T C 20 GENIC homozygous 960887803 5 29577571 29577572 T G 17 GENIC homozygous 960887804 5 29577572 29577573 T C 18 GENIC homozygous 960887805 5 29579092 29579093 A G 24 GENIC homozygous 960887806 5 29580623 29580624 C T 40 GENIC homozygous 960887807 5 29581045 29581046 A C 17 GENIC homozygous 960887808 5 29584953 29584954 G A 19 GENIC homozygous 960887809 5 29585702 29585703 G A 18 GENIC homozygous 960887810 5 29586006 29586007 G T 26 GENIC homozygous 960887811 5 29586260 29586261 C T 33 GENIC homozygous 960887812 5 29586265 29586266 C T 35 GENIC homozygous 960887813 5 29586720 29586721 C T 31 GENIC homozygous 960887814 5 29586750 29586751 G A 35 GENIC homozygous 960887815 5 29588819 29588820 C T 27 GENIC possibly homozygous 960887816 5 29588830 29588831 C T 26 GENIC homozygous 960887817 5 29594156 29594157 T C 17 GENIC homozygous 960887818 5 29599622 29599623 G A 32 GENIC homozygous 960887819 5 29600649 29600650 T C 19 GENIC homozygous 960887820 5 29600995 29600996 A G 12 GENIC homozygous 960887821 5 29601081 29601082 G A 12 GENIC homozygous 960887822 5 29601656 29601657 C T 16 GENIC homozygous 960887823