chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	213885060	213885061	A	C	39	GENIC	homozygous	108532098
1	213885274	213885275	T	C	25	GENIC	homozygous	108532103
1	213885572	213885573	G	A	28	GENIC	homozygous	108532104
1	213886034	213886035	G	A	33	GENIC	homozygous	108532105
1	213886414	213886415	A	G	27	GENIC	homozygous	108532106
1	213887070	213887071	G	A	20	GENIC	homozygous	108532107
1	213887285	213887286	A	G	24	GENIC	homozygous	108532108
1	213887856	213887857	A	T	17	GENIC	homozygous	108532109
1	213888171	213888172	G	C	18	GENIC	homozygous	108532110
1	213888508	213888509	G	T	28	GENIC	homozygous	108532111
1	213890408	213890409	A	G	28	GENIC	homozygous	108532112
1	213890487	213890488	C	G	23	GENIC	homozygous	108532113
1	213893036	213893037	C	T	34	GENIC	homozygous	108532114
1	213893489	213893490	G	A	10	GENIC	homozygous	108532118
1	213894158	213894159	G	C	30	GENIC	homozygous	108532121
1	213894282	213894283	T	C	24	GENIC	homozygous	108532122
1	213894527	213894528	A	G	34	GENIC	homozygous	108532123
1	213895761	213895762	T	C	16	GENIC	homozygous	108532124
1	213896124	213896125	G	A	25	GENIC	homozygous	108532125
1	213896806	213896807	C	T	16	GENIC	homozygous	108532126