chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	153921783	153921784	C	T	26	GENIC	homozygous	56989520
4	153921928	153921929	A	-	25	GENIC	possibly homozygous	56989521
4	153922217	153922218	C	T	27	GENIC	homozygous	56989522
4	153923011	153923012	T	C	12	GENIC	homozygous	56989523
4	153923019	153923020	G	C	9	GENIC	homozygous	58347582
4	153923203	153923204	G	A	27	GENIC	homozygous	56989526
4	153924866	153924867	A	G	33	GENIC	homozygous	56989527
4	153925267	153925268	C	T	35	GENIC	homozygous	56989528
4	153925311	153925312	C	T	30	GENIC	homozygous	56989529
4	153925838	153925839	G	A	36	GENIC	homozygous	56989530
4	153925876	153925877	A	G	35	GENIC	homozygous	56989531
4	153925904	153925905	A	C	35	GENIC	homozygous	56989532
4	153925922	153925923	A	C	35	GENIC	homozygous	56989533
4	153927816	153927820	ACAA	----	9	GENIC	heterozygous	58821590
4	153927956	153927957	C	T	20	GENIC	homozygous	56989534
4	153928180	153928181	G	GTAA	32	GENIC	homozygous	56989535
4	153929260	153929261	A	-	7	GENIC	heterozygous	58407776
4	153929869	153929870	T	TAC	16	GENIC	heterozygous	56989537
4	153930161	153930162	C	T	18	GENIC	homozygous	56989539
4	153930347	153930348	T	TTG	7	GENIC	heterozygous	56989540
4	153930354	153930356	TG	--	7	GENIC	heterozygous	58595071
4	153932761	153932762	C	T	25	GENIC	homozygous	56989541
4	153936452	153936453	C	T	12	GENIC	homozygous	58286985
4	153936453	153936454	T	C	12	GENIC	homozygous	58286987
4	153936462	153936463	A	-	12	GENIC	homozygous	56989542
4	153936887	153936888	C	G	8	GENIC	homozygous	56989543
4	153938083	153938084	T	G	28	GENIC	homozygous	56989544
4	153940599	153940600	T	-	31	GENIC	homozygous	56989545
4	153941224	153941225	G	-	7	GENIC	heterozygous	56989546