chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	164114693	164114694	A	G	39	GENIC	homozygous	108350131
1	164117099	164117101	TC		23	GENIC	homozygous	127452233
1	164117122	164117123	G	C	22	GENIC	homozygous	108350135
1	164117132	164117133	C		19	GENIC	homozygous	127452234
1	164117138	164117140	CA		19	GENIC	homozygous	127452235
1	164117141	164117141		C	19	GENIC	homozygous	127452236
1	164117163	164117163		A	15	GENIC	homozygous	127452237
1	164117201	164117202	A		15	GENIC	homozygous	127452238
1	164117259	164117260	C		18	GENIC	homozygous	127452239
1	164117264	164117265	C		19	GENIC	homozygous	127452240
1	164117270	164117271	G		18	GENIC	homozygous	127452241
1	164117276	164117277	C		18	GENIC	homozygous	127452242
1	164117281	164117282	T		18	GENIC	homozygous	127452243
1	164117286	164117286		T	19	GENIC	homozygous	127452244
1	164117299	164117301	CT		21	GENIC	homozygous	127452245
1	164117312	164117314	TA		21	GENIC	homozygous	127452246
1	164117329	164117330	T	A	22	GENIC	homozygous	108350137
1	164117332	164117333	A		22	GENIC	homozygous	127452247
1	164119385	164119386	G	C	18	GENIC	homozygous	109435060
1	164120629	164120630	C	T	25	GENIC	homozygous	109435062
1	164141006	164141007	T	C	35	GENIC	homozygous	108350218
1	164141090	164141091	T	C	33	GENIC	homozygous	109435064