chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	122606563	122606564	T	C	30	GENIC	homozygous	108923471
1	122607474	122607475	A	G	7	GENIC	homozygous	108209584
1	122616097	122616098	G	A	22	GENIC	homozygous	108923496
1	122631110	122631111	C	T	37	GENIC	homozygous	108209779
1	122631722	122631723	T	C	43	GENIC	homozygous	108209796
1	122631764	122631765	A	G	26	GENIC	homozygous	108209797
1	122632919	122632920	T	C	16	GENIC	homozygous	108209802
1	122633242	122633243	A	G	18	GENIC	homozygous	108209804
1	122655875	122655876	C	T	28	GENIC	homozygous	108209882
1	122657567	122657568	T	C	29	GENIC	homozygous	108209905
1	122657761	122657762	T	C	41	GENIC	homozygous	108209906
1	122665505	122665506	G	C	18	GENIC	homozygous	108209945
1	122668640	122668641	C	T	29	GENIC	homozygous	108210029
1	122671230	122671231	G	A	17	GENIC	homozygous	108210096
1	122671562	122671563	C	T	23	GENIC	homozygous	108210097
1	122671612	122671613	A	G	17	GENIC	homozygous	108210098
1	122671844	122671845	T	C	29	GENIC	homozygous	108210099
1	122672619	122672620	A	C	28	GENIC	homozygous	108210100
1	122672621	122672622	G	A	28	GENIC	homozygous	108210101
1	122673064	122673065	T	C	34	GENIC	homozygous	108210103
1	122674968	122674969	G	C	20	GENIC	homozygous	108210116
1	122675675	122675676	T	C	17	GENIC	homozygous	108923554