chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	154781114	154781115	C	G	26	GENIC	homozygous	114062619
5	154782235	154782236	C	T	4	GENIC	homozygous	114062625
5	154782437	154782438	G	A	17	GENIC	homozygous	114062627
5	154782441	154782442	A	C	14	GENIC	homozygous	114062629
5	154782501	154782502	A	G	14	GENIC	homozygous	114062631
5	154782502	154782503	A	C	14	GENIC	homozygous	114062633
5	154783139	154783140	G	C	32	GENIC	homozygous	114062635
5	154783602	154783603	T	C	17	GENIC	homozygous	114062639
5	154784154	154784155	G	A	28	GENIC	homozygous	114062641
5	154784267	154784268	T	G	21	GENIC	homozygous	114062643
5	154784480	154784481	G	A	28	GENIC	homozygous	114062645
5	154785831	154785832	T	C	28	GENIC	homozygous	114158743
5	154788791	154788792	A	G	29	GENIC	homozygous	114158745
5	154790464	154790465	T	G	31	GENIC	homozygous	114158746
5	154791726	154791727	C	T	27	GENIC	homozygous	114158747
5	154794574	154794575	G	A	30	GENIC	homozygous	114158750
5	154795006	154795007	A	G	28	GENIC	homozygous	114062669
5	154796471	154796472	C	T	21	GENIC	homozygous	114062671
5	154797804	154797805	G	A	30	GENIC	homozygous	114062675
5	154799292	154799293	G	A	38	GENIC	homozygous	114062679
5	154799390	154799391	C	G	25	GENIC	homozygous	114158751
5	154799962	154799963	T	A	26	GENIC	homozygous	114062681
5	154800016	154800017	T	G	27	GENIC	homozygous	114062683