chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	167289945	167289945		AA	60	GENIC	homozygous	130964694
5	167291555	167291555		AGCTCACA	56	GENIC	homozygous	130964695
5	167292008	167292020	ACGGGTGTCTTA		65	GENIC	homozygous	130964696
5	167292906	167292907	A	C	34	GENIC	homozygous	114283140
5	167291101	167291102	G	A	53	GENIC	homozygous	114283130
5	167292251	167292252	A	G	49	GENIC	homozygous	114283134
5	167292492	167292493	C	T	50	GENIC	homozygous	114283136
5	167292755	167292756	C	T	38	GENIC	homozygous	114283138
5	167293182	167293183	C	T	43	GENIC	homozygous	114283142
5	167293420	167293421	T	C	53	GENIC	homozygous	114283144
5	167293442	167293443	A	G	52	GENIC	homozygous	114283146
5	167293646	167293647	G	A	50	GENIC	homozygous	114283148
5	167294642	167294643	G	T	69	GENIC	homozygous	114283150
5	167295366	167295367	T	C	76	GENIC	homozygous	114283156
5	167295871	167295873	TT		81	GENIC	homozygous	130964697
5	167296089	167296090	C	T	53	GENIC	homozygous	114283160
5	167293076	167293077	T	C	19	GENIC	homozygous	130972555
5	167293637	167293638	T	C	43	GENIC	homozygous	114082276
5	167296624	167296624		T	55	GENIC	homozygous	130964698
5	167297042	167297043	G	T	69	GENIC	homozygous	114283162
5	167297045	167297046	A	C	68	GENIC	homozygous	114283164
5	167297521	167297522	G	A	67	GENIC	homozygous	114283166
5	167298753	167298753		TCT	39	GENIC	homozygous	130964699
5	167296109	167296110	G	A	51	GENIC	homozygous	114455247
5	167297809	167297810	G	A	59	GENIC	homozygous	114283168
5	167299502	167299503	C	T	60	GENIC	homozygous	114283170
5	167293014	167293015	C	A	15	GENIC	homozygous	114455245
5	167295634	167295635	G	T	56	GENIC	homozygous	114455246
5	167293072	167293073	C		20	GENIC	homozygous	128269778