chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	255371870	255371871	C	T	19	GENIC	homozygous	108617971
1	255372070	255372071	G	C	12	GENIC	homozygous	108617973
1	255372089	255372090	A	G	12	GENIC	homozygous	108617974
1	255372110	255372111	G	A	7	GENIC	homozygous	108617976
1	255372114	255372115	T	G	8	GENIC	homozygous	108617977
1	255372196	255372197	C	T	18	GENIC	homozygous	108617979
1	255372227	255372228	T	C	17	GENIC	homozygous	108617981
1	255372314	255372315	C	T	12	GENIC	homozygous	108617982
1	255372482	255372483	T	C	18	GENIC	homozygous	108617984
1	255372587	255372588	C	T	11	GENIC	homozygous	108617985
1	255372595	255372596	C	T	6	GENIC	homozygous	108617987
1	255372613	255372614	A	G	16	GENIC	homozygous	108617988
1	255372701	255372702	A	G	27	GENIC	homozygous	108617990
1	255372756	255372757	C	T	14	GENIC	homozygous	108617991
1	255373172	255373173	G	C	16	GENIC	homozygous	108617993
1	255373198	255373199	C	G	16	GENIC	homozygous	108617994
1	255373274	255373275	T	C	6	GENIC	homozygous	108617996
1	255373797	255373798	G	A	18	GENIC	homozygous	108617998
1	255373983	255373984	A	G	9	GENIC	homozygous	108617999
1	255374016	255374017	G	C	13	GENIC	homozygous	108618001
1	255374167	255374168	G	A	21	GENIC	homozygous	108618002
1	255374905	255374906	C	A	5	GENIC	heterozygous	108618004
1	255375068	255375069	T	C	13	GENIC	homozygous	108618006
1	255375415	255375416	T	A	21	GENIC	homozygous	108618007