chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	84135667	84135668	A	G	29	GENIC	homozygous	70875052
4	84136253	84136254	C	T	26	GENIC	possibly homozygous	70875055
4	84137538	84137539	C	T	32	GENIC	homozygous	72428559
4	84137640	84137641	C	T	30	GENIC	homozygous	70875064
4	84137930	84137931	T	C	17	GENIC	homozygous	72428563
4	84137950	84137951	T	C	20	GENIC	possibly homozygous	72428567
4	84138114	84138115	C	T	20	GENIC	possibly homozygous	72428571
4	84138706	84138707	A	C	18	GENIC	possibly homozygous	70875073
4	84140305	84140306	T	A	28	GENIC	homozygous	70875076
4	84140837	84140838	T	G	27	GENIC	homozygous	70875079
4	84142282	84142283	C	G	25	GENIC	possibly homozygous	70875082
4	84144078	84144079	G	A	27	GENIC	homozygous	70875085
4	84144339	84144340	A	T	28	GENIC	homozygous	70875087
4	84144447	84144448	T	C	17	GENIC	homozygous	70875090
4	84146369	84146370	T	C	14	GENIC	homozygous	70875093
4	84146402	84146403	G	A	22	GENIC	homozygous	72428575
4	84146932	84146933	T	C	22	GENIC	possibly homozygous	70875096
4	84148259	84148260	A	G	15	GENIC	homozygous	70875124