chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 88126664 88126669 TTTTG 37 GENIC heterozygous 130867155 2 88126674 88126674 G 40 GENIC homozygous 127648745 2 88127355 88127356 T C 54 GENIC homozygous 109898794 2 88127631 88127632 A G 50 GENIC homozygous 109898796 2 88129334 88129335 C A 35 GENIC homozygous 109898798 2 88129431 88129432 A G 41 GENIC possibly homozygous 109898800 2 88129845 88129846 G A 48 GENIC homozygous 109898802 2 88131432 88131433 T C 59 GENIC homozygous 109898803 2 88132375 88132376 G A 58 GENIC homozygous 109898805 2 88132402 88132403 A G 59 GENIC homozygous 109898807 2 88133184 88133185 T A 41 GENIC homozygous 109898809 2 88134078 88134078 G 45 GENIC homozygous 127648746 2 88134389 88134390 G A 57 GENIC homozygous 109898811 2 88134410 88134411 T C 50 GENIC homozygous 109898813 2 88134951 88134952 A G 34 GENIC homozygous 109898814