chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	9537583	9537584	T	C	30	GENIC	homozygous	112490437
4	9537838	9537839	G	A	24	GENIC	homozygous	112490439
4	9538101	9538102	G	C	24	GENIC	homozygous	112490441
4	9538207	9538208	G	C	22	GENIC	homozygous	113078026
4	9537697	9537698	T	A	33	GENIC	heterozygous	113078021
4	9537721	9537722	G	C	27	GENIC	possibly homozygous	113078023
4	9538206	9538207	G	C	23	GENIC	possibly homozygous	113078025
4	9538374	9538375	T	G	17	GENIC	homozygous	112490443
4	9538377	9538378	A	G	17	GENIC	heterozygous	113078027
4	9538451	9538452	G	A	31	GENIC	heterozygous	113078029
4	9538498	9538499	T	A	24	GENIC	heterozygous	113078031
4	9538507	9538508	G	A	23	GENIC	heterozygous	113078032
4	9538527	9538528	A	G	17	GENIC	homozygous	112490450
4	9538576	9538577	C	G	43	GENIC	heterozygous	113078033
4	9538619	9538620	G	A	53	GENIC	heterozygous	113078035
4	9538630	9538631	C	T	53	GENIC	heterozygous	113078036
4	9538658	9538659	C	G	39	GENIC	heterozygous	113078038
4	9538721	9538722	A	G	20	GENIC	homozygous	112490456
4	9538798	9538799	G	C	10	GENIC	homozygous	113078040
4	9538830	9538831	G	A	13	GENIC	homozygous	112490460
4	9538923	9538924	G	A	34	GENIC	heterozygous	113078041
4	9538942	9538943	T	A	26	GENIC	heterozygous	113078043
4	9538945	9538946	C	G	22	GENIC	homozygous	112490468
4	9538956	9538957	G	A	17	GENIC	heterozygous	112490470
4	9539022	9539023	T	A	9	GENIC	heterozygous	113078045
4	9539130	9539131	A	T	23	GENIC	heterozygous	112490476
4	9539140	9539141	G	T	35	GENIC	heterozygous	113078046
4	9539152	9539153	C	G	51	GENIC	heterozygous	112490477
4	9539197	9539198	A	T	141	GENIC	heterozygous	112490479
4	9539198	9539199	A	G	141	GENIC	heterozygous	112490481
4	9539270	9539271	T	A	78	GENIC	heterozygous	112490483
4	9539292	9539293	T	C	14	GENIC	homozygous	112490485
4	9539242	9539243	T	A	120	GENIC	heterozygous	112996758