chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 78190395 78190395 G 29 GENIC possibly homozygous 127396723 1 78190396 78190397 T 30 GENIC heterozygous 127396724 1 78190420 78190420 T 35 GENIC homozygous 127396725 1 78190754 78190755 C 34 GENIC homozygous 127396726 1 78190788 78190788 G 31 GENIC homozygous 127396727 1 78190792 78190793 C 29 GENIC homozygous 127396728 1 78190827 78190828 A G 21 GENIC homozygous 120472112 1 78190828 78190829 G A 20 GENIC homozygous 120481016 1 78190847 78190848 C 18 GENIC homozygous 127396729 1 78190865 78190865 T 12 GENIC homozygous 127396730 1 78190873 78190874 C T 8 GENIC homozygous 108728718 1 78190875 78190876 T 8 GENIC homozygous 127396731 1 78192871 78192873 AC 37 GENIC homozygous 127396732 1 78192921 78192922 C 39 GENIC homozygous 127396733 1 78192935 78192935 A 45 GENIC homozygous 127396734 1 78192948 78192949 A 46 GENIC homozygous 127396735 1 78192960 78192961 G 47 GENIC homozygous 127396736 1 78192967 78192968 G 47 GENIC homozygous 127396737 1 78192982 78192984 GC 43 GENIC homozygous 127396738 1 78192999 78193000 T 41 GENIC homozygous 127396739 1 78193018 78193019 C 40 GENIC homozygous 127396740 1 78193020 78193021 T 41 GENIC homozygous 127396741