chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	58363724	58363725	G	T	11	GENIC	possibly homozygous	47146504
17	58365489	58365490	T	C	20	GENIC	homozygous	47146505
17	58366468	58366469	C	-	15	GENIC	homozygous	47146507
17	58366577	58366578	C	T	22	GENIC	possibly homozygous	47146509
17	58367795	58367796	C	T	14	GENIC	homozygous	47146510
17	58369085	58369086	C	T	17	GENIC	possibly homozygous	47146512
17	58369196	58369197	G	A	25	GENIC	homozygous	47146514
17	58370161	58370162	C	T	21	GENIC	homozygous	47146515
17	58372055	58372056	T	C	11	GENIC	possibly homozygous	47146519
17	58373186	58373187	G	T	4	GENIC	homozygous	47146520
17	58376064	58376065	T	C	11	GENIC	heterozygous	47146522
17	58377513	58377514	C	A	6	GENIC	homozygous	47146524
17	58380382	58380383	A	AT	1	GENIC	homozygous	47146525
17	58383063	58383064	T	C	22	GENIC	possibly homozygous	47146527
17	58384164	58384165	A	-	2	GENIC	homozygous	47146531
17	58390354	58390355	A	G	10	GENIC	heterozygous	47146536