chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	253220779	253220780	G	T	34	GENIC	homozygous	108613421
1	253221278	253221279	G	T	28	GENIC	homozygous	109020563
1	253226385	253226386	A	G	3	GENIC	homozygous	109020565
1	253234653	253234654	G	A	23	GENIC	homozygous	109020568
1	253237038	253237039	T	A	12	GENIC	homozygous	132558194
1	253237875	253237876	C	A	20	GENIC	homozygous	109020569
1	253238542	253238543	T	C	37	GENIC	homozygous	108613423
1	253240576	253240577	G	A	25	GENIC	homozygous	109020570
1	253241685	253241686	C	T	24	GENIC	homozygous	109020571
1	253244881	253244882	G	T	27	GENIC	homozygous	109020572
1	253249753	253249754	C	T	32	GENIC	homozygous	109020573
1	253253233	253253234	G	A	22	GENIC	homozygous	109020574
1	253254073	253254074	G	A	28	GENIC	homozygous	109020575
1	253224265	253224265		CTC	4	GENIC	homozygous	132935644
1	253244666	253244667	C	T	32	GENIC	homozygous	108613426
1	253253186	253253187	C	T	20	GENIC	homozygous	108613427
1	253253477	253253478	T	C	19	GENIC	homozygous	108613428
1	253260086	253260087	A	G	12	GENIC	homozygous	109020577
1	253265098	253265099	A	G	16	GENIC	homozygous	108613441
1	253268209	253268210	A	C	23	GENIC	homozygous	109020579
1	253272689	253272689		CTCCTCCTCCCA	10	GENIC	homozygous	132542077
1	253272718	253272719	C		10	GENIC	homozygous	131266600