chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	146924200	146924201	A	G	27	GENIC	homozygous	112873747
4	146924555	146924556	G	A	38	GENIC	homozygous	113394374
4	146924822	146924823	C	T	41	GENIC	homozygous	113394376
4	146926799	146926800	T	C	22	GENIC	homozygous	113180091
4	146927088	146927089	A	G	43	GENIC	homozygous	112873749
4	146928922	146928923	A	G	21	GENIC	homozygous	112873750
4	146929263	146929264	C	T	33	GENIC	homozygous	113394378
4	146930568	146930569	T	C	14	GENIC	homozygous	112873752
4	146932544	146932545	T	C	19	GENIC	homozygous	112873754
4	146932641	146932642	C	T	14	GENIC	homozygous	112873755
4	146933680	146933681	T	C	27	GENIC	homozygous	112873756
4	146933975	146933976	C	T	35	GENIC	homozygous	113394380
4	146934087	146934088	G	T	45	GENIC	homozygous	113394382
4	146934115	146934116	T	G	35	GENIC	homozygous	112873757
4	146936175	146936176	T	C	25	GENIC	homozygous	113394384
4	146936262	146936263	A	G	30	GENIC	homozygous	113394386
4	146936346	146936347	A	G	26	GENIC	homozygous	113394388
4	146936379	146936380	T	C	31	GENIC	homozygous	113394390
4	146936461	146936462	T	C	28	GENIC	homozygous	113394392
4	146940904	146940905	C	T	37	GENIC	homozygous	113394394
4	146944735	146944736	G	C	43	GENIC	homozygous	113394396
4	146944814	146944815	T	C	39	GENIC	homozygous	113180102
4	146944835	146944836	C	T	36	GENIC	homozygous	113394398
4	146946058	146946059	T	C	17	GENIC	homozygous	113180105
4	146946272	146946273	A	G	22	GENIC	homozygous	113180106
4	146946408	146946409	C	T	22	GENIC	homozygous	112873771
4	146946875	146946876	C	T	20	GENIC	homozygous	113180108
4	146946988	146946989	G	A	18	GENIC	homozygous	113394402
4	146947778	146947779	T	C	32	GENIC	homozygous	113180109
4	146948636	146948637	G	A	19	GENIC	homozygous	113394404
4	146948720	146948721	G	A	31	GENIC	homozygous	113180110