chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	131011277	131011278	C	-	10	GENIC	homozygous	57677912
3	131011820	131011821	G	C	17	GENIC	homozygous	57677914
3	131014014	131014015	C	A	17	GENIC	homozygous	57677920
3	131014235	131014239	CAGA	----	10	GENIC	homozygous	57677922
3	131015451	131015452	T	C	20	GENIC	homozygous	57677926
3	131015572	131015573	T	C	16	GENIC	homozygous	57677928
3	131015791	131015792	C	T	14	GENIC	homozygous	57677930
3	131016835	131016836	T	C	14	GENIC	homozygous	57677936
3	131017390	131017391	A	T	22	GENIC	homozygous	57677938
3	131017701	131017702	A	G	19	GENIC	homozygous	57677940
3	131017787	131017788	G	GCT	19	GENIC	homozygous	57677942
3	131017845	131017846	C	T	22	GENIC	homozygous	57677943
3	131018010	131018011	T	-	12	GENIC	homozygous	57677945
3	131018182	131018183	C	A	12	GENIC	homozygous	57677947
3	131019069	131019070	A	G	18	GENIC	homozygous	57677949
3	131019094	131019095	C	T	18	GENIC	homozygous	57677951
3	131019275	131019276	G	A	12	GENIC	homozygous	57677953
3	131020111	131020112	T	C	10	GENIC	homozygous	57677957
3	131020178	131020179	A	C	13	GENIC	homozygous	57677959
3	131020198	131020199	G	A	17	GENIC	homozygous	57677961
3	131020240	131020241	C	T	14	GENIC	homozygous	57677963
3	131021119	131021123	TTGA	----	10	GENIC	homozygous	57677967
3	131022445	131022446	T	C	18	GENIC	homozygous	57677971
3	131022486	131022487	T	C	11	GENIC	homozygous	57677973
3	131024554	131024555	A	T	17	GENIC	homozygous	57677977
3	131025138	131025139	G	A	18	GENIC	homozygous	57677979