chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 117920930 117920931 G A 7 GENIC homozygous 116672626 8 117921471 117921472 G T 13 GENIC homozygous 117920438 8 117923231 117923232 T G 18 GENIC homozygous 117920441 8 117923566 117923567 T C 12 GENIC homozygous 116672632 8 117923661 117923662 G A 13 GENIC homozygous 116672634 8 117923713 117923714 C T 17 GENIC homozygous 117969054 8 117923801 117923802 G A 13 GENIC homozygous 117969055 8 117923869 117923870 T G 12 GENIC homozygous 116672636 8 117923986 117923987 C T 17 GENIC homozygous 117969056 8 117924081 117924082 C T 10 GENIC homozygous 123049910 8 117924094 117924095 C T 10 GENIC homozygous 123049911 8 117924632 117924633 A G 12 GENIC homozygous 116672638 8 117924728 117924729 G A 12 GENIC homozygous 116672640 8 117925148 117925149 T C 13 GENIC homozygous 116672642 8 117925751 117925752 C T 5 GENIC homozygous 116887245 8 117926305 117926306 A C 15 GENIC homozygous 116887249 8 117927564 117927565 A G 21 GENIC homozygous 116887251 8 117927690 117927691 C T 11 GENIC homozygous 116887253 8 117924500 117924502 CA 6 GENIC homozygous 128636045 8 117924509 117924511 GA 7 GENIC homozygous 131054434 8 117928102 117928104 CC 18 GENIC homozygous 131054435