chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	6618226	6618227	C	T	25	GENIC	possibly homozygous	111869965
3	6618497	6618498	G	A	29	GENIC	possibly homozygous	111869967
3	6620289	6620290	A	G	30	GENIC	homozygous	111869969
3	6620335	6620336	A	G	22	GENIC	homozygous	111869971
3	6620462	6620463	T	C	26	GENIC	possibly homozygous	111869973
3	6620669	6620670	A	G	25	GENIC	possibly homozygous	111869976
3	6620897	6620898	G	A	18	GENIC	homozygous	111869978
3	6621077	6621078	A	G	18	GENIC	possibly homozygous	111869981
3	6621705	6621706	C	T	19	GENIC	homozygous	111869983
3	6621767	6621768	T	G	22	GENIC	homozygous	111869985
3	6622202	6622203	T	C	24	GENIC	homozygous	111869987
3	6623567	6623568	C	T	19	GENIC	homozygous	111869995
3	6624453	6624454	G	A	21	GENIC	homozygous	111869997
3	6625223	6625224	C	T	21	GENIC	possibly homozygous	111869999
3	6625472	6625473	C	A	21	GENIC	homozygous	111870001
3	6625502	6625503	G	C	24	GENIC	homozygous	111870003
3	6625576	6625577	C	A	19	GENIC	homozygous	111870005
3	6625795	6625796	T	A	18	GENIC	possibly homozygous	111870007
3	6626013	6626014	G	A	14	GENIC	homozygous	111870009