chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	216256712	216256713	G	A	38	GENIC	homozygous	109193132
1	216257031	216257032	G	A	22	GENIC	homozygous	109193134
1	216257174	216257175	T	C	34	GENIC	homozygous	109193136
1	216257450	216257451	A	G	36	GENIC	homozygous	108535669
1	216258379	216258380	T	C	28	GENIC	homozygous	109193138
1	216258471	216258472	G	A	29	GENIC	homozygous	109193140
1	216258516	216258517	T	C	30	GENIC	homozygous	108535671
1	216258532	216258533	G	A	28	GENIC	homozygous	109193142
1	216260173	216260174	G	A	25	GENIC	homozygous	109193146
1	216262145	216262146	T	G	37	GENIC	homozygous	108535673
1	216262146	216262147	C	T	37	GENIC	homozygous	120490504
1	216262484	216262485	A	G	38	GENIC	homozygous	108535675
1	216263228	216263229	G	A	19	GENIC	homozygous	109193148
1	216264012	216264013	T	C	31	GENIC	homozygous	108535676
1	216264534	216264535	A	C	32	GENIC	homozygous	108535677
1	216264583	216264584	A	G	38	GENIC	homozygous	108535678
1	216266509	216266510	C	T	38	GENIC	homozygous	109193150
1	216266889	216266890	G	A	37	GENIC	homozygous	109193152
1	216268775	216268776	G	C	21	GENIC	homozygous	108535684
1	216269220	216269221	T	C	30	GENIC	homozygous	108535685
1	216270191	216270192	T	G	36	GENIC	homozygous	108535687
1	216270300	216270301	A	G	32	GENIC	homozygous	108535688
1	216275563	216275564	A	G	27	GENIC	homozygous	108535692
1	216277048	216277049	T	C	26	GENIC	homozygous	108535693