chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 167289945 167289945 AA 30 GENIC homozygous 130964694 5 167291101 167291102 G A 43 GENIC homozygous 114283130 5 167291555 167291555 AGCTCACA 38 GENIC homozygous 130964695 5 167292008 167292020 ACGGGTGTCTTA 41 GENIC homozygous 130964696 5 167292251 167292252 A G 41 GENIC homozygous 114283134 5 167292492 167292493 C T 49 GENIC homozygous 114283136 5 167292755 167292756 C T 35 GENIC homozygous 114283138 5 167292906 167292907 A C 37 GENIC homozygous 114283140 5 167293182 167293183 C T 39 GENIC homozygous 114283142 5 167293420 167293421 T C 36 GENIC homozygous 114283144 5 167293442 167293443 A G 33 GENIC homozygous 114283146 5 167293646 167293647 G A 39 GENIC homozygous 114283148 5 167294642 167294643 G T 44 GENIC homozygous 114283150 5 167295366 167295367 T C 45 GENIC homozygous 114283156 5 167295871 167295873 TT 50 GENIC homozygous 130964697 5 167296089 167296090 C T 55 GENIC homozygous 114283160 5 167296624 167296624 T 39 GENIC homozygous 130964698 5 167297042 167297043 G T 53 GENIC homozygous 114283162 5 167297045 167297046 A C 51 GENIC homozygous 114283164 5 167297521 167297522 G A 40 GENIC homozygous 114283166 5 167297809 167297810 G A 49 GENIC homozygous 114283168 5 167298753 167298753 TCT 42 GENIC homozygous 130964699 5 167299502 167299503 C T 47 GENIC homozygous 114283170 5 167292514 167292515 C T 47 GENIC homozygous 134696130 5 167293014 167293015 C A 23 GENIC homozygous 114455245 5 167295634 167295635 G T 33 GENIC homozygous 114455246 5 167296109 167296110 G A 52 GENIC homozygous 114455247 5 167293072 167293073 C 30 GENIC homozygous 128269778 5 167293076 167293077 T C 29 GENIC possibly homozygous 130972555 5 167293637 167293638 T C 36 GENIC homozygous 114082276