chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 138854764 138854765 G A 49 GENIC homozygous 533323863 3 138854888 138854889 T C 48 GENIC homozygous 533323864 3 138854941 138854942 A G 52 GENIC homozygous 533323865 3 138855369 138855370 A ATGTGTGTGTGTGTG 34 GENIC homozygous 695423107 3 138855386 138855387 T TG 39 GENIC heterozygous 695423109 3 138855389 138855390 T TG 39 GENIC heterozygous 695423110 3 138855675 138855676 G A 55 GENIC homozygous 533323866 3 138855737 138855738 C T 61 GENIC heterozygous 535807835 3 138855737 138855738 C CAT 55 GENIC possibly homozygous 695423111 3 138855739 138855740 C T 62 GENIC possibly homozygous 535807836 3 138855867 138855868 T C 51 GENIC heterozygous 533323867 3 138855899 138855900 C CAT 41 GENIC heterozygous 695423112 3 138856662 138856676 TGTGTGTGTGTGTC -------------- 23 GENIC homozygous 695423113 3 138857442 138857443 T A 57 GENIC possibly homozygous 533323868 3 138857627 138857629 AA -- 22 GENIC homozygous 695423114 3 138858255 138858256 C CT 20 GENIC homozygous 695423115 3 138858273 138858274 C CTT 17 GENIC homozygous 695423116 3 138859276 138859277 A C 40 GENIC possibly homozygous 533323869 3 138860556 138860557 C T 53 GENIC homozygous 533323870