chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	206343620	206343621	T	A	11	GENIC	homozygous	61066628
1	206343886	206343887	G	C	12	GENIC	homozygous	61066629
1	206344033	206344034	G	A	17	GENIC	homozygous	61066630
1	206345046	206345047	A	G	34	GENIC	homozygous	61066631
1	206345105	206345106	A	T	33	GENIC	homozygous	61066632
1	206345374	206345375	A	G	31	GENIC	homozygous	61066633
1	206346538	206346539	A	C	22	GENIC	homozygous	61066634
1	206348414	206348415	G	T	25	GENIC	homozygous	61066635
1	206348476	206348477	T	A	13	GENIC	homozygous	61066636
1	206350130	206350131	A	G	14	GENIC	homozygous	61066637
1	206351958	206351959	A	G	19	GENIC	homozygous	61066638
1	206352232	206352233	T	-	19	GENIC	possibly homozygous	61318396
1	206352626	206352627	T	-	21	GENIC	homozygous	61066639
1	206352702	206352703	T	A	14	GENIC	homozygous	61066640
1	206352823	206352824	G	A	14	GENIC	homozygous	61066641
1	206352895	206352896	C	CA	20	GENIC	homozygous	61066642
1	206353067	206353068	T	A	25	GENIC	homozygous	61066643
1	206353642	206353643	C	-	13	GENIC	possibly homozygous	61066644