chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 181434866 181434867 A G 9 GENIC homozygous 954890823 4 181435720 181435721 G A 19 GENIC homozygous 954890824 4 181435781 181435782 C A 23 GENIC homozygous 954890825 4 181436610 181436611 A G 17 GENIC homozygous 954890826 4 181436843 181436844 G A 19 GENIC homozygous 954890827 4 181437267 181437268 C T 33 GENIC homozygous 954890828 4 181437268 181437269 T C 32 GENIC homozygous 954890829 4 181437397 181437398 G A 32 GENIC homozygous 954890830 4 181441039 181441040 A T 21 GENIC homozygous 954890831 4 181442797 181442798 T C 27 GENIC homozygous 954890832 4 181443370 181443371 G A 35 GENIC homozygous 954890833 4 181443970 181443971 G T 23 GENIC homozygous 954890834 4 181445032 181445033 A C 20 GENIC homozygous 954890835 4 181445509 181445510 T G 27 GENIC homozygous 954890836 4 181446043 181446044 C T 30 GENIC homozygous 954890837 4 181446672 181446673 C T 25 GENIC homozygous 954890838 4 181448706 181448707 C T 26 GENIC homozygous 954890839 4 181448896 181448897 C T 30 GENIC homozygous 954890840 4 181452682 181452683 C T 23 GENIC homozygous 954890841 4 181454787 181454788 G A 37 INTERGENIC possibly homozygous 954890842 4 181462026 181462027 C T 11 INTERGENIC homozygous 954890843 4 181463422 181463423 G A 32 INTERGENIC homozygous 954890844 4 181464930 181464931 T C 32 INTERGENIC homozygous 954890845