chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	153926342	153926343	G	A	11	GENIC	homozygous	57522071
4	153926418	153926419	A	G	23	GENIC	possibly homozygous	57522073
4	153926510	153926511	C	A	24	GENIC	homozygous	57843880
4	153926891	153926892	G	A	18	GENIC	homozygous	57843881
4	153927448	153927449	G	C	25	GENIC	possibly homozygous	57522075
4	153928946	153928947	C	CTTTG	2	GENIC	heterozygous	57522077
4	153929077	153929078	C	T	18	GENIC	homozygous	57522079
4	153929406	153929407	C	T	13	GENIC	homozygous	57522081
4	153929686	153929687	G	A	19	GENIC	possibly homozygous	57522083
4	153932133	153932134	T	TATGCCA	5	GENIC	homozygous	57522089
4	153932761	153932762	C	T	4	GENIC	homozygous	56989541
4	153933394	153933395	G	C	7	GENIC	homozygous	57843886
4	153934300	153934301	G	A	18	GENIC	homozygous	57843887
4	153934926	153934927	A	G	11	GENIC	homozygous	57843888
4	153934980	153934981	G	A	12	GENIC	homozygous	57843889
4	153935434	153935435	C	A	4	GENIC	homozygous	57843890
4	153936341	153936342	T	TGAA	3	GENIC	homozygous	57843891
4	153936350	153936351	G	A	2	GENIC	homozygous	57843892
4	153936452	153936453	C	T	2	GENIC	homozygous	58286985
4	153936453	153936454	T	C	2	GENIC	homozygous	58286987
4	153936675	153936676	A	G	20	GENIC	homozygous	57522091
4	153936887	153936888	C	G	27	GENIC	possibly homozygous	56989543
4	153937840	153937841	A	C	20	GENIC	homozygous	57522093
4	153937868	153937869	A	G	18	GENIC	homozygous	57522095
4	153938083	153938084	T	G	9	GENIC	homozygous	56989544
4	153938130	153938131	G	A	12	GENIC	heterozygous	57522097
4	153938700	153938701	G	A	6	GENIC	heterozygous	57522099
4	153939376	153939377	G	A	17	GENIC	homozygous	57522101
4	153940057	153940058	G	T	6	GENIC	homozygous	57522103
4	153940192	153940193	A	G	16	GENIC	homozygous	57522107
4	153940532	153940533	G	A	20	GENIC	homozygous	57522109
4	153940598	153940599	A	AT	3	GENIC	homozygous	57522111