chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	213885060	213885061	A	C	9	GENIC	homozygous	108532098
1	213885125	213885126	C	A	18	GENIC	homozygous	108532099
1	213885274	213885275	T	C	20	GENIC	homozygous	108532103
1	213885572	213885573	G	A	17	GENIC	homozygous	108532104
1	213886034	213886035	G	A	17	GENIC	homozygous	108532105
1	213886414	213886415	A	G	10	GENIC	homozygous	108532106
1	213887070	213887071	G	A	13	GENIC	homozygous	108532107
1	213887285	213887286	A	G	13	GENIC	homozygous	108532108
1	213887856	213887857	A	T	12	GENIC	homozygous	108532109
1	213888171	213888172	G	C	8	GENIC	homozygous	108532110
1	213890408	213890409	A	G	12	GENIC	homozygous	108532112
1	213890487	213890488	C	G	10	GENIC	homozygous	108532113
1	213893036	213893037	C	T	12	GENIC	homozygous	108532114
1	213893356	213893357	A	T	8	GENIC	homozygous	108532116
1	213893368	213893369	G	C	9	GENIC	homozygous	108532117
1	213893489	213893490	G	A	13	GENIC	homozygous	108532118
1	213894158	213894159	G	C	32	GENIC	homozygous	108532121
1	213894282	213894283	T	C	27	GENIC	homozygous	108532122
1	213894527	213894528	A	G	17	GENIC	homozygous	108532123
1	213895761	213895762	T	C	12	GENIC	homozygous	108532124
1	213896124	213896125	G	A	6	GENIC	homozygous	108532125
1	213896806	213896807	C	T	9	GENIC	homozygous	108532126