chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	157501907	157501908	A	G	26	GENIC	homozygous	114069927
5	157501918	157501919	A	C	25	GENIC	homozygous	114069928
5	157502472	157502473	G	A	39	GENIC	homozygous	114069929
5	157502596	157502597	C	T	19	GENIC	homozygous	114069930
5	157502700	157502701	T	C	36	GENIC	homozygous	114069931
5	157502935	157502936	C	T	32	GENIC	homozygous	114069932
5	157503102	157503103	A	G	24	GENIC	homozygous	114069933
5	157503113	157503114	T	C	27	GENIC	homozygous	114069934
5	157503124	157503125	T	A	26	GENIC	homozygous	114069935
5	157503173	157503174	G	A	23	GENIC	homozygous	114069936
5	157505507	157505508	A	G	40	GENIC	homozygous	114069939
5	157505679	157505680	C	T	28	GENIC	homozygous	114069940
5	157505989	157505990	A	T	6	GENIC	homozygous	118858891
5	157506344	157506345	A	G	32	GENIC	homozygous	114069943
5	157507439	157507440	A	G	33	GENIC	homozygous	114069944
5	157508028	157508029	C	G	34	GENIC	homozygous	114069945
5	157509553	157509554	C	T	19	GENIC	homozygous	114069946
5	157509705	157509706	C	T	37	GENIC	homozygous	114069947
5	157509809	157509810	A	G	38	GENIC	homozygous	114069948
5	157509977	157509978	T	A	8	GENIC	homozygous	114069949
5	157510395	157510396	C	T	27	GENIC	homozygous	114069950
5	157510454	157510455	C	T	37	GENIC	homozygous	114069951
5	157510499	157510500	G	A	34	GENIC	homozygous	114069952
5	157510501	157510502	C	T	33	GENIC	homozygous	114069953
5	157510665	157510666	G	A	26	GENIC	homozygous	114069954
5	157510680	157510681	G	C	22	GENIC	homozygous	114069955
5	157510710	157510711	G	A	19	GENIC	homozygous	114069956
5	157510747	157510748	C	T	23	GENIC	homozygous	114069957
5	157510946	157510947	G	T	39	GENIC	homozygous	114069958