chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	82182609	82182610	T	C	13	GENIC	homozygous	109880115
2	82182736	82182737	C	A	18	GENIC	homozygous	109880116
2	82182854	82182855	T	C	11	GENIC	possibly homozygous	109880118
2	82182900	82182901	C	T	14	GENIC	possibly homozygous	109880119
2	82182935	82182936	T	G	17	GENIC	possibly homozygous	109880120
2	82182981	82182982	G	A	13	GENIC	homozygous	109880121
2	82182982	82182983	C	T	12	GENIC	homozygous	109880122
2	82183006	82183007	G	A	15	GENIC	homozygous	109880123
2	82183182	82183183	C	T	15	GENIC	homozygous	109880124
2	82183261	82183262	C	A	14	GENIC	homozygous	109880125
2	82183350	82183351	A	G	12	GENIC	homozygous	109880126
2	82183404	82183405	C	T	11	GENIC	homozygous	109880127
2	82183454	82183455	C	T	12	GENIC	homozygous	109880128
2	82183491	82183492	C	A	14	GENIC	homozygous	109880129