chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	145549577	145549578	G	A	20	GENIC	homozygous	113179030
4	145550319	145550320	A	C	22	GENIC	homozygous	113179031
4	145550569	145550570	G	A	22	GENIC	homozygous	113179032
4	145550868	145550869	G	T	16	GENIC	homozygous	113179033
4	145550931	145550932	A	G	22	GENIC	homozygous	113179034
4	145550995	145550996	A	G	28	GENIC	homozygous	113179035
4	145551013	145551014	G	T	32	GENIC	homozygous	113179036
4	145551188	145551189	T	C	42	GENIC	homozygous	113179037
4	145551276	145551277	G	A	31	GENIC	homozygous	113179038
4	145551513	145551514	A	G	34	GENIC	homozygous	113179039
4	145551516	145551517	A	G	33	GENIC	homozygous	113179040
4	145551729	145551730	T	C	36	GENIC	homozygous	112871097
4	145551739	145551740	A	G	33	GENIC	homozygous	113179041
4	145551806	145551807	G	A	22	GENIC	homozygous	113179042
4	145552266	145552267	T	G	23	GENIC	homozygous	113179043
4	145552741	145552742	C	A	24	GENIC	homozygous	113179044
4	145552908	145552909	T	C	34	GENIC	homozygous	113179045
4	145553948	145553949	G	T	29	GENIC	homozygous	112871100
4	145553961	145553962	G	A	30	GENIC	homozygous	113179046
4	145554224	145554225	A	G	38	GENIC	homozygous	112871102
4	145554622	145554623	A	C	21	GENIC	homozygous	112871103
4	145554939	145554940	C	T	23	GENIC	homozygous	112871105
4	145554940	145554941	C	G	23	GENIC	homozygous	112871106
4	145555452	145555453	T	C	40	GENIC	homozygous	112871107
4	145555501	145555502	C	T	44	GENIC	homozygous	112871108
4	145555710	145555711	A	G	37	GENIC	homozygous	112871109
4	145555932	145555933	C	G	32	GENIC	homozygous	112871110