chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	82182581	82182582	G	A	41	GENIC	homozygous	110715689
2	82182582	82182583	A	G	41	GENIC	homozygous	120125269
2	82182854	82182855	T	C	26	GENIC	homozygous	109880118
2	82182609	82182610	T	C	36	GENIC	homozygous	109880115
2	82182736	82182737	C	A	12	GENIC	homozygous	109880116
2	82182799	82182800	T	C	17	GENIC	homozygous	109880117
2	82182900	82182901	C	T	25	GENIC	homozygous	109880119
2	82182982	82182983	C	T	23	GENIC	homozygous	109880122
2	82182935	82182936	T	G	25	GENIC	homozygous	109880120
2	82182981	82182982	G	A	23	GENIC	homozygous	109880121
2	82183006	82183007	G	A	24	GENIC	homozygous	109880123
2	82183182	82183183	C	T	32	GENIC	homozygous	109880124
2	82183261	82183262	C	A	24	GENIC	homozygous	109880125
2	82183350	82183351	A	G	44	GENIC	homozygous	109880126
2	82183362	82183363	A	G	43	GENIC	homozygous	120125270
2	82183363	82183364	C	A	44	GENIC	homozygous	120125271
2	82183404	82183405	C	T	42	GENIC	homozygous	109880127
2	82183454	82183455	C	T	43	GENIC	homozygous	109880128
2	82183491	82183492	C	A	36	GENIC	homozygous	109880129