chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	208492701	208492702	G	-	15	GENIC	heterozygous	58675161
4	208492833	208492834	A	-	13	GENIC	heterozygous	58410592
4	208493985	208493986	T	G	32	GENIC	homozygous	58487495
4	208492880	208492881	A	G	12	GENIC	homozygous	57066601
4	208495077	208495078	A	G	25	GENIC	homozygous	57066602
4	208497974	208497976	TT	--	16	GENIC	heterozygous	58369113
4	208497975	208497976	T	-	16	GENIC	heterozygous	58369115
4	208498471	208498472	T	C	17	GENIC	homozygous	57066605
4	208498924	208498925	T	C	18	GENIC	homozygous	57066606
4	208499666	208499667	C	CT	8	GENIC	homozygous	58369117
4	208501729	208501730	A	G	11	GENIC	homozygous	58487496
4	208501737	208501738	A	G	12	GENIC	homozygous	58487497
4	208504805	208504806	G	C	35	GENIC	homozygous	58487498
4	208505297	208505298	T	C	20	GENIC	homozygous	57066610
4	208507287	208507288	C	T	31	GENIC	homozygous	58487499
4	208510543	208510544	T	C	29	GENIC	homozygous	57066613
4	208512238	208512239	A	-	7	GENIC	homozygous	57066614
4	208512868	208512869	G	T	34	GENIC	homozygous	58487500
4	208512907	208512908	T	C	31	GENIC	homozygous	57066615
4	208515226	208515227	A	AT	20	GENIC	possibly homozygous	58487501
4	208515943	208515944	A	G	31	GENIC	homozygous	57066616
4	208518017	208518018	T	A	26	GENIC	possibly homozygous	58487502
4	208522353	208522354	T	C	29	GENIC	homozygous	57066620
4	208522657	208522658	A	C	29	GENIC	possibly homozygous	58487503
4	208523079	208523080	A	G	26	GENIC	homozygous	57066621
4	208525385	208525386	C	A	30	GENIC	homozygous	58487504
4	208526012	208526013	A	G	24	GENIC	homozygous	58487505
4	208529860	208529861	G	C	32	GENIC	homozygous	57066623
4	208530351	208530353	AA	--	26	GENIC	heterozygous	58369123
4	208530352	208530353	A	-	26	GENIC	heterozygous	58487506
4	208531115	208531116	G	A	30	GENIC	homozygous	58487507
4	208533558	208533559	A	G	26	GENIC	homozygous	57066628