chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 100990278 100990279 C T 20 GENIC homozygous 114437747 13 100991019 100991020 A G 16 GENIC homozygous 114437749 13 100991268 100991269 C A 20 GENIC homozygous 114437751 13 100991291 100991292 A C 18 GENIC homozygous 114437753 13 100991442 100991443 A G 33 GENIC homozygous 114437755 13 100991443 100991444 G C 32 GENIC homozygous 114437757 13 101024473 101024474 G A 38 GENIC homozygous 114437759 13 101031631 101031632 G C 16 GENIC homozygous 114437761 13 101031634 101031635 A T 16 GENIC homozygous 114437763 13 101031924 101031925 G A 33 GENIC homozygous 114437765 13 101032161 101032162 A G 20 GENIC homozygous 114437767 13 101032162 101032163 G A 20 GENIC homozygous 114585097 13 101032289 101032290 C T 13 GENIC homozygous 115032956