chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	154781114	154781115	C	G	36	GENIC	homozygous	114062619
5	154782235	154782236	C	T	27	GENIC	homozygous	114062625
5	154782437	154782438	G	A	26	GENIC	homozygous	114062627
5	154782441	154782442	A	C	26	GENIC	homozygous	114062629
5	154782501	154782502	A	G	26	GENIC	homozygous	114062631
5	154782502	154782503	A	C	26	GENIC	homozygous	114062633
5	154783139	154783140	G	C	38	GENIC	homozygous	114062635
5	154783365	154783366	A	C	26	GENIC	homozygous	114062637
5	154783602	154783603	T	C	34	GENIC	homozygous	114062639
5	154784154	154784155	G	A	24	GENIC	homozygous	114062641
5	154784267	154784268	T	G	22	GENIC	homozygous	114062643
5	154784480	154784481	G	A	30	GENIC	homozygous	114062645
5	154785981	154785982	G	A	29	GENIC	homozygous	114357935
5	154786026	154786027	A	G	29	GENIC	homozygous	114357937
5	154786736	154786737	T	C	42	GENIC	homozygous	114357939
5	154787188	154787189	T	C	9	GENIC	possibly homozygous	114062655
5	154788236	154788237	C	T	31	GENIC	homozygous	114357941
5	154789553	154789554	C	T	34	GENIC	possibly homozygous	114062657
5	154789557	154789558	T	C	34	GENIC	possibly homozygous	114062659
5	154791726	154791727	C	T	20	GENIC	homozygous	114158747
5	154791952	154791953	G	A	45	GENIC	heterozygous	114062661
5	154792877	154792878	C	T	36	GENIC	heterozygous	114357943
5	154792881	154792882	C	T	37	GENIC	heterozygous	114357945
5	154795006	154795007	A	G	19	GENIC	homozygous	114062669
5	154795971	154795972	G	A	31	GENIC	homozygous	114357947
5	154796471	154796472	C	T	28	GENIC	homozygous	114062671
5	154797804	154797805	G	A	20	GENIC	homozygous	114062675
5	154799292	154799293	G	A	22	GENIC	homozygous	114062679
5	154799962	154799963	T	A	9	GENIC	homozygous	114062681
5	154800016	154800017	T	G	30	GENIC	homozygous	114062683