chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	50003658	50003659	C	T	17	GENIC	homozygous	114401785
5	50003718	50003719	C	T	7	GENIC	homozygous	114500738
5	50004157	50004158	C	T	10	GENIC	homozygous	114500741
5	50007534	50007535	G	A	8	GENIC	homozygous	114401795
5	50007864	50007865	G	A	15	GENIC	homozygous	114500743
5	50008157	50008158	T	C	20	GENIC	possibly homozygous	114401797
5	50008624	50008625	G	A	14	GENIC	homozygous	113791449
5	50009365	50009366	A	C	4	GENIC	homozygous	113791450
5	50010244	50010245	A	G	10	GENIC	homozygous	114401799
5	50010911	50010912	T	A	6	GENIC	homozygous	113791451
5	50011170	50011171	A	T	12	GENIC	possibly homozygous	114401803
5	50011441	50011442	C	T	18	GENIC	homozygous	114401805
5	50011499	50011500	C	T	20	GENIC	possibly homozygous	114401807
5	50011655	50011656	A	T	11	GENIC	homozygous	114401809
5	50014258	50014259	A	T	10	GENIC	homozygous	114200484
5	50015968	50015969	C	T	22	GENIC	homozygous	114500745