chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 44313659 44313660 C CTGCT 1 GENIC homozygous 705581558 1 44313662 44313666 ATGA ---- 3 GENIC homozygous 705581559 1 44313723 44313724 A AGTGCGCG 2 GENIC homozygous 705581560 1 44313725 44313728 CAA --- 3 GENIC homozygous 705581562 1 44313729 44313730 C T 2 GENIC homozygous 561849537 1 44313731 44313732 G GC 2 GENIC homozygous 705581563 1 44313733 44313734 T TTA 2 GENIC homozygous 705581564 1 44313735 44313736 T TGGTG 2 GENIC homozygous 705581565 1 44313863 44313864 T C 13 GENIC homozygous 561849538 1 44313868 44313869 A C 13 GENIC homozygous 561849539 1 44313875 44313876 T TTA 17 GENIC homozygous 705581566 1 44313878 44313879 G A 18 GENIC homozygous 561849540 1 44313880 44313881 A T 18 GENIC homozygous 561849541 1 44313884 44313888 TCAT ---- 21 GENIC homozygous 705581567 1 44313912 44313913 C T 29 GENIC homozygous 561849542 1 44313919 44313926 CCCTTGT ------- 38 GENIC homozygous 705581568 1 44313952 44313953 G T 46 GENIC homozygous 561849543 1 44313963 44313964 G T 47 GENIC homozygous 561849544