chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	167931560	167931561	C	G	4	GENIC	heterozygous	140965535
1	167959598	167959599	A	G	21	GENIC	homozygous	140965536
1	168016559	168016560	A	T	18	GENIC	heterozygous	402971954
1	168016559	168016560	A		18	GENIC	possibly homozygous	402971955
1	168122215	168122216	A	C	28	GENIC	homozygous	135740284
1	168203561	168203562	C	G	20	GENIC	heterozygous	402971984
1	168016561	168016562	A	T	18	GENIC	heterozygous	402971956
1	168016561	168016562	A		18	GENIC	possibly homozygous	402971957
1	168122221	168122222	T		29	GENIC	heterozygous	402971966
1	168122221	168122222	T	G	29	GENIC	homozygous	402971967
1	168203561	168203562	C		20	GENIC	heterozygous	402971983
1	168205573	168205573		GATA	31	GENIC	homozygous	140958772
1	168089841	168089842	G		34	GENIC	possibly homozygous	140958770
1	168203361	168203363	GT		20	GENIC	possibly homozygous	140958771
1	168206212	168206213	T		14	GENIC	possibly homozygous	403545250
1	168206212	168206213	T	C	14	GENIC	heterozygous	403545251
1	168212074	168212075	C	G	31	GENIC	homozygous	135740448
1	168212078	168212079	C	T	31	GENIC	homozygous	135740449
1	168212084	168212085	C	T	29	GENIC	possibly homozygous	135740450
1	168225654	168225655	C	G	21	GENIC	heterozygous	140965537
1	168225661	168225662	C	A	20	GENIC	heterozygous	402971987
1	168225661	168225662	C		20	GENIC	homozygous	402971988
1	168225669	168225670	T	A	21	GENIC	homozygous	402971989
1	168225669	168225670	T		21	GENIC	heterozygous	402971990
1	168225679	168225680	C	A	20	GENIC	homozygous	402971991
1	168225679	168225680	C		20	GENIC	heterozygous	402971992
1	168225685	168225686	T	A	20	GENIC	homozygous	402971993
1	168225685	168225686	T		20	GENIC	heterozygous	402971994
1	168203795	168203796	T	C	38	GENIC	homozygous	147245330