chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	10930305	10930306	C	A	24	GENIC	homozygous	57150986
3	10930607	10930608	C	T	19	GENIC	possibly homozygous	57150988
3	10930942	10930943	T	C	19	GENIC	homozygous	57150990
3	10931064	10931065	C	T	27	GENIC	possibly homozygous	57150992
3	10931599	10931600	C	T	24	GENIC	possibly homozygous	57150994
3	10932428	10932429	C	T	22	GENIC	homozygous	57150996
3	10932566	10932567	T	C	10	GENIC	heterozygous	57150998
3	10932638	10932639	G	A	33	GENIC	possibly homozygous	57151000
3	10932939	10932940	C	T	26	GENIC	homozygous	57151002
3	10933004	10933005	C	T	20	GENIC	possibly homozygous	57151004
3	10933023	10933024	A	G	16	GENIC	homozygous	57151006
3	10933309	10933310	T	C	12	GENIC	homozygous	57151008
3	10933368	10933369	C	T	17	GENIC	homozygous	57151010
3	10933394	10933395	G	T	14	GENIC	possibly homozygous	57151012
3	10934116	10934117	T	TC	14	GENIC	homozygous	57151016
3	10934139	10934140	C	G	24	GENIC	possibly homozygous	57151018
3	10934169	10934170	A	G	21	GENIC	possibly homozygous	57151020
3	10934238	10934239	G	C	14	GENIC	homozygous	57151022
3	10934796	10934797	T	C	17	GENIC	possibly homozygous	57151024
3	10935282	10935284	TC	--	5	GENIC	homozygous	57151026
3	10935284	10935285	C	G	5	GENIC	homozygous	58991877
3	10935765	10935768	CTG	---	5	GENIC	homozygous	57151028
3	10935799	10935800	T	C	6	GENIC	heterozygous	58991879
3	10935800	10935801	C	T	6	GENIC	heterozygous	58991882
3	10936498	10936499	G	A	17	GENIC	heterozygous	57151030
3	10936652	10936653	T	G	11	GENIC	homozygous	57151032