chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 40497663 40497664 A C 26 GENIC homozygous 961732028 10 40497696 40497697 G A 26 GENIC homozygous 961732029 10 40497808 40497809 G A 27 GENIC homozygous 961732030 10 40498617 40498618 G A 11 GENIC homozygous 961732031 10 40498619 40498620 A G 11 GENIC homozygous 961732032 10 40500411 40500412 A G 18 GENIC homozygous 961732033 10 40500473 40500474 G T 27 GENIC homozygous 961732034 10 40500850 40500851 G A 22 GENIC homozygous 961732035 10 40502101 40502102 G C 14 GENIC homozygous 961732036 10 40502767 40502768 G A 41 GENIC possibly homozygous 961732037 10 40502880 40502881 A G 44 GENIC homozygous 961732038 10 40503317 40503318 T C 25 GENIC homozygous 961732039 10 40503320 40503321 T C 25 GENIC homozygous 961732040 10 40507861 40507862 T C 21 GENIC homozygous 961732041 10 40519700 40519701 G A 41 GENIC homozygous 961732042 10 40521385 40521386 G A 22 GENIC homozygous 961732043 10 40521734 40521735 T A 29 GENIC homozygous 961732044 10 40522019 40522020 C T 21 GENIC homozygous 961732045 10 40522778 40522779 T C 17 GENIC homozygous 961732046 10 40522871 40522872 C T 15 GENIC homozygous 961732047 10 40524890 40524891 A C 27 GENIC homozygous 961732048