chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	90067488	90067496	GGTGAGCT	--------	46	GENIC	possibly homozygous	62245452
1	90069369	90069370	G	T	57	GENIC	homozygous	62712174
1	90069885	90069886	A	C	22	GENIC	possibly homozygous	61887578
1	90069910	90069911	T	C	19	GENIC	heterozygous	62140236
1	90069939	90069940	T	C	14	GENIC	heterozygous	62140237
1	90070139	90070140	G	A	15	GENIC	homozygous	62140238
1	90070385	90070386	T	C	23	GENIC	homozygous	62534790
1	90071290	90071292	AA	--	4	GENIC	homozygous	62245453
1	90071852	90071853	T	C	21	GENIC	homozygous	61461326
1	90072898	90072899	C	CTTT	9	GENIC	heterozygous	61887582
1	90072898	90072899	C	CTT	9	GENIC	heterozygous	62140240
1	90072927	90072928	A	G	17	GENIC	homozygous	61461328
1	90072928	90072929	C	G	17	GENIC	homozygous	61461330
1	90073212	90073213	A	G	52	GENIC	homozygous	61461331
1	90074096	90074097	A	G	18	GENIC	possibly homozygous	61461333
1	90074436	90074437	T	C	20	GENIC	homozygous	61461335
1	90075371	90075372	A	G	58	GENIC	homozygous	61887586