chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 44313659 44313660 C CTGCT 7 GENIC homozygous 765748490 1 44313662 44313666 ATGA ---- 12 GENIC homozygous 765748491 1 44313723 44313724 A AGTGCGCG 15 GENIC heterozygous 765748492 1 44313723 44313724 A AGTGCGTG 15 GENIC heterozygous 765748493 1 44313725 44313728 CAA --- 18 GENIC homozygous 765748494 1 44313729 44313730 C T 16 GENIC homozygous 664372908 1 44313731 44313732 G GC 17 GENIC homozygous 765748495 1 44313733 44313734 T TTA 18 GENIC homozygous 765748496 1 44313735 44313736 T TGGTG 18 GENIC homozygous 765748497 1 44313863 44313864 T C 40 GENIC heterozygous 664372909 1 44313868 44313869 A C 42 GENIC heterozygous 664372910 1 44313875 44313876 T TTA 47 GENIC heterozygous 765748498 1 44313878 44313879 G A 52 GENIC heterozygous 664372911 1 44313880 44313881 A T 53 GENIC heterozygous 664372912 1 44313884 44313888 TCAT ---- 56 GENIC heterozygous 765748499 1 44313912 44313913 C T 62 GENIC heterozygous 664372913 1 44313919 44313926 CCCTTGT ------- 69 GENIC heterozygous 765748500 1 44313952 44313953 G T 76 GENIC possibly homozygous 664372914 1 44313963 44313964 G T 75 GENIC possibly homozygous 664372915