chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 49889353 49889354 G GGTGTGTGTGTGTGTGTGT 13 GENIC homozygous 50513821 12 49890647 49890648 A ACC 2 GENIC homozygous 50513823 12 49890689 49890690 A AC 5 GENIC heterozygous 50235075 12 49891718 49891730 ACACACACACAC ------------ 5 GENIC heterozygous 50546756 12 49891720 49891730 ACACACACAC ---------- 5 GENIC heterozygous 50546757 12 49891952 49891953 T C 38 GENIC homozygous 50235079 12 49892515 49892516 A G 31 GENIC homozygous 50235081 12 49892564 49892565 C CG 32 GENIC homozygous 50235083 12 49892994 49892995 A G 42 GENIC homozygous 50235085 12 49893006 49893007 C T 39 GENIC homozygous 50235087 12 49897028 49897029 G T 35 GENIC homozygous 50235093 12 49893666 49893667 G A 31 GENIC homozygous 50235089 12 49895907 49895908 A C 29 GENIC homozygous 50235091 12 49897105 49897106 G C 32 GENIC homozygous 50235095 12 49899043 49899044 T C 24 GENIC homozygous 50235097 12 49899940 49899941 A AATAGGTAAGGGGTAGCTAGAAATGGGGACACTGAGACTGGTCAGGTCACACAGGTT 37 GENIC homozygous 50546758 12 49900592 49900593 C T 17 GENIC homozygous 50235099 12 49900691 49900692 G A 32 GENIC homozygous 50235101 12 49902577 49902578 G A 17 GENIC homozygous 50235103 12 49903130 49903131 C A 54 GENIC homozygous 50235105 12 49903419 49903420 A AATGCACACACATACAC 4 GENIC heterozygous 50546759 12 49903481 49903482 C CGCATGCACACACATAA 60 GENIC possibly homozygous 50546760 12 49904879 49904883 AAAA ---- 10 GENIC homozygous 50235119 12 49904882 49904883 A ACC 9 GENIC homozygous 50546761 12 49905167 49905168 G A 34 GENIC homozygous 50235121 12 49907140 49907141 A T 18 GENIC homozygous 50235123