chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	205960328	205960329	G	-	2	GENIC	heterozygous	61065912
1	205961237	205961238	C	CT	2	GENIC	heterozygous	61065916
1	205961528	205961529	C	T	16	GENIC	possibly homozygous	61065917
1	205962491	205962492	A	G	19	GENIC	heterozygous	61065918
1	205963051	205963052	T	C	15	GENIC	homozygous	61065919
1	205963203	205963204	G	C	17	GENIC	possibly homozygous	61065920
1	205963384	205963385	G	GA	10	GENIC	possibly homozygous	61065921
1	205963593	205963594	A	-	4	GENIC	homozygous	61065923
1	205963919	205963920	T	C	17	GENIC	possibly homozygous	61065924
1	205964510	205964511	A	G	29	GENIC	homozygous	61065928
1	205965266	205965267	A	-	3	GENIC	heterozygous	61065929
1	205966908	205966909	G	A	20	GENIC	homozygous	61065931
1	205967626	205967630	AAAT	----	6	GENIC	heterozygous	61065933
1	205968469	205968470	G	A	21	GENIC	possibly homozygous	61065938
1	205969956	205969957	G	T	14	GENIC	homozygous	61065943
1	205980247	205980248	G	T	20	GENIC	possibly homozygous	61065948
1	205982040	205982042	TA	--	8	GENIC	homozygous	61065949
1	205984175	205984176	A	-	19	GENIC	homozygous	61065950
1	205985266	205985267	A	T	20	GENIC	homozygous	61065951
1	206004448	206004449	G	GT	2	GENIC	homozygous	62030736
1	206004902	206004903	T	G	17	GENIC	homozygous	61065956
1	206005015	206005016	A	AT	2	GENIC	heterozygous	62248623
1	206009701	206009702	A	G	35	GENIC	homozygous	61065961
1	206007330	206007331	G	T	18	GENIC	homozygous	61065958
1	206009313	206009314	T	A	11	GENIC	possibly homozygous	61065959
1	206009666	206009667	A	G	30	GENIC	possibly homozygous	61065960
1	206010477	206010478	T	C	10	GENIC	possibly homozygous	61065962
1	206012558	206012559	C	T	9	GENIC	heterozygous	61065963
1	206015431	206015432	A	AAC	1	GENIC	homozygous	61065967