chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	153921334	153921335	G	A	21	GENIC	possibly homozygous	58161385
4	153921573	153921574	T	A	3	GENIC	heterozygous	58161387
4	153921719	153921720	T	C	16	GENIC	homozygous	57956465
4	153921753	153921754	C	T	19	GENIC	homozygous	59132769
4	153923011	153923012	T	C	6	GENIC	heterozygous	56989523
4	153923019	153923020	G	C	4	GENIC	heterozygous	58347582
4	153924049	153924050	A	C	18	GENIC	possibly homozygous	57956471
4	153925311	153925312	C	T	26	GENIC	homozygous	56989529
4	153925876	153925877	A	G	11	GENIC	possibly homozygous	56989531
4	153926342	153926343	G	A	12	GENIC	heterozygous	57522071
4	153926418	153926419	A	G	13	GENIC	heterozygous	57522073
4	153927448	153927449	G	C	20	GENIC	possibly homozygous	57522075
4	153928946	153928947	C	CTTTG	1	GENIC	homozygous	57522077
4	153929077	153929078	C	T	18	GENIC	homozygous	57522079
4	153929406	153929407	C	T	12	GENIC	possibly homozygous	57522081
4	153929686	153929687	G	A	26	GENIC	possibly homozygous	57522083
4	153931372	153931373	A	G	4	GENIC	homozygous	58476136
4	153932133	153932134	T	TATGCCA	2	GENIC	homozygous	57522089
4	153932761	153932762	C	T	4	GENIC	homozygous	56989541
4	153936462	153936463	A	-	2	GENIC	heterozygous	56989542
4	153936477	153936478	A	AC	3	GENIC	heterozygous	57743083
4	153936478	153936479	C	-	3	GENIC	heterozygous	58476138
4	153936887	153936888	C	G	20	GENIC	possibly homozygous	56989543
4	153938083	153938084	T	G	18	GENIC	homozygous	56989544
4	153938969	153938970	G	T	14	GENIC	possibly homozygous	58476142
4	153940599	153940600	T	-	7	GENIC	heterozygous	56989545
4	153941224	153941225	G	-	1	GENIC	homozygous	56989546
4	153936452	153936453	C	T	3	GENIC	heterozygous	58286985
4	153936453	153936454	T	C	3	GENIC	heterozygous	58286987