chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	159253989	159253990	T	C	15	GENIC	homozygous	58481711
4	159254359	159254360	C	A	6	GENIC	homozygous	57001003
4	159254602	159254603	A	G	12	GENIC	possibly homozygous	58169836
4	159255526	159255527	A	C	18	GENIC	possibly homozygous	57001006
4	159256559	159256560	C	T	15	GENIC	homozygous	58481713
4	159256848	159256849	C	G	21	GENIC	possibly homozygous	58169846
4	159257359	159257360	A	C	20	GENIC	homozygous	57001007
4	159257590	159257591	C	T	6	GENIC	heterozygous	57001009
4	159264219	159264220	A	G	13	GENIC	homozygous	57001052
4	159264226	159264227	T	-	11	GENIC	homozygous	58481715
4	159264857	159264858	T	C	15	GENIC	homozygous	57001057
4	159266117	159266118	G	C	1	GENIC	homozygous	57001065
4	159267358	159267359	C	T	7	GENIC	homozygous	58481719
4	159267430	159267431	C	CA	2	GENIC	heterozygous	58481721
4	159268110	159268111	C	T	14	GENIC	homozygous	58169868
4	159268962	159268963	T	-	2	GENIC	homozygous	58481723
4	159270499	159270501	AC	--	1	GENIC	homozygous	57001099
4	159273694	159273695	T	G	2	GENIC	homozygous	57001108
4	159275677	159275678	T	C	10	GENIC	heterozygous	57001113
4	159277265	159277266	G	A	14	GENIC	possibly homozygous	58481729
4	159278898	159278899	A	C	13	GENIC	homozygous	58169898
4	159280737	159280738	A	AG	12	GENIC	homozygous	57001124
4	159281546	159281547	T	C	10	GENIC	homozygous	57001126
4	159281727	159281728	T	C	12	GENIC	possibly homozygous	57001127
4	159282182	159282183	T	C	3	GENIC	heterozygous	58481733
4	159284779	159284780	T	C	7	GENIC	heterozygous	57001134
4	159287075	159287076	A	G	15	GENIC	homozygous	58481737
4	159268015	159268016	T	-	3	GENIC	heterozygous	58445239