chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	121010108	121010109	T	A	26	GENIC	homozygous	108921816
1	121010474	121010475	G	A	36	GENIC	heterozygous	108739732
1	121010491	121010492	C	A	42	GENIC	heterozygous	108202137
1	121010497	121010498	C	A	40	GENIC	heterozygous	108202138
1	121010509	121010510	A	C	39	GENIC	heterozygous	108202139
1	121010517	121010518	T	G	39	GENIC	heterozygous	108739733
1	121010546	121010547	T	A	31	GENIC	heterozygous	108739734
1	121010749	121010750	C	T	22	GENIC	homozygous	108921817
1	121010948	121010949	G	T	20	GENIC	homozygous	108921818
1	121011254	121011255	A	T	23	GENIC	homozygous	108921819
1	121011790	121011791	A	G	25	GENIC	homozygous	108921820
1	121013404	121013405	A	T	23	GENIC	homozygous	108921821
1	121014402	121014403	T	A	34	GENIC	homozygous	108921822
1	121014713	121014714	T	A	26	GENIC	homozygous	108921823
1	121015636	121015637	A	G	17	GENIC	homozygous	108202141
1	121015768	121015769	C	A	24	GENIC	homozygous	108921824