chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	201068076	201068077	C	A	34	GENIC	homozygous	59339746
2	201068288	201068289	T	C	27	GENIC	homozygous	61768003
2	201068346	201068347	G	A	22	GENIC	homozygous	59339749
2	201068679	201068680	C	T	33	GENIC	homozygous	59339751
2	201068770	201068771	T	C	44	GENIC	homozygous	59339756
2	201069082	201069083	A	G	30	GENIC	homozygous	59339758
2	201069140	201069141	A	G	30	GENIC	homozygous	61768005
2	201069221	201069222	T	A	25	GENIC	homozygous	59339760
2	201069371	201069372	G	C	27	GENIC	homozygous	61768007
2	201069426	201069427	G	-	34	GENIC	homozygous	61768009
2	201069828	201069829	C	T	45	GENIC	homozygous	61768011
2	201070187	201070188	A	G	30	GENIC	homozygous	61768013
2	201070303	201070304	T	C	36	GENIC	homozygous	61768015
2	201070592	201070593	A	G	35	GENIC	homozygous	59339763
2	201071197	201071198	C	T	26	GENIC	homozygous	61768017
2	201071690	201071692	TT	--	26	GENIC	homozygous	61768019
2	201071696	201071698	TT	--	28	GENIC	homozygous	61768021
2	201072647	201072648	G	T	27	GENIC	homozygous	61768023
2	201072997	201072998	A	C	40	GENIC	homozygous	59339772
2	201073058	201073059	A	G	37	GENIC	homozygous	59339773
2	201073496	201073497	T	-	20	GENIC	homozygous	61768025
2	201074076	201074077	G	T	22	GENIC	homozygous	61768027
2	201075110	201075111	C	T	30	GENIC	homozygous	61768029
2	201075131	201075132	T	C	28	GENIC	homozygous	59339778