chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	172161487	172161488	G	A	15	GENIC	heterozygous	111837276
3	172161488	172161489	C	G	15	GENIC	heterozygous	121923383
3	172161512	172161513	C	G	13	GENIC	heterozygous	112047191
3	172161520	172161521	T	G	14	GENIC	heterozygous	121923384
3	172161524	172161525	T	C	14	GENIC	heterozygous	121923385
3	172161525	172161526	T	C	14	GENIC	heterozygous	121923386
3	172161526	172161527	T	A	14	GENIC	heterozygous	121923387
3	172161532	172161533	A	G	15	GENIC	heterozygous	121923388
3	172161541	172161542	G		14	GENIC	heterozygous	127961983
3	172162099	172162100	A	T	10	GENIC	heterozygous	127996643
3	172162940	172162940		GTTATG	14	GENIC	homozygous	127961984
3	172170209	172170210	T	G	11	GENIC	heterozygous	112047192
3	172170227	172170228	C	A	14	GENIC	heterozygous	111837278
3	172170788	172170789	T		39	GENIC	heterozygous	127961985
3	172171358	172171359	G	A	55	GENIC	heterozygous	127996644
3	172171386	172171387	T	C	61	GENIC	heterozygous	127996645
3	172171676	172171677	C		48	GENIC	heterozygous	127961986
3	172171678	172171679	A	T	47	GENIC	heterozygous	121923402
3	172172107	172172108	C	A	44	GENIC	heterozygous	127996646
3	172172113	172172114	T	C	44	GENIC	heterozygous	127996647
3	172172121	172172122	G	T	49	GENIC	heterozygous	127996648
3	172176191	172176192	C		39	GENIC	homozygous	127961987
3	172176206	172176207	G		43	GENIC	homozygous	127961988
3	172176226	172176228	CC		45	GENIC	homozygous	127961989
3	172176232	172176234	CC		42	GENIC	homozygous	127961990
3	172177347	172177348	G	T	14	GENIC	homozygous	111837284