chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	208492701	208492702	G	-	6	GENIC	heterozygous	58675161
4	208494215	208494216	C	A	20	GENIC	homozygous	59172820
4	208498924	208498925	T	C	6	GENIC	homozygous	57066606
4	208492880	208492881	A	G	19	GENIC	homozygous	57066601
4	208495077	208495078	A	G	11	GENIC	homozygous	57066602
4	208498471	208498472	T	C	12	GENIC	heterozygous	57066605
4	208501705	208501706	C	CT	2	GENIC	heterozygous	58600891
4	208504257	208504258	G	-	17	GENIC	homozygous	59172824
4	208504805	208504806	G	C	13	GENIC	possibly homozygous	58487498
4	208504989	208504990	G	A	16	GENIC	homozygous	59172826
4	208505297	208505298	T	C	13	GENIC	homozygous	57066610
4	208510543	208510544	T	C	20	GENIC	possibly homozygous	57066613
4	208511143	208511147	CTCT	----	8	GENIC	homozygous	59172828
4	208512907	208512908	T	C	28	GENIC	homozygous	57066615
4	208513452	208513453	A	G	18	GENIC	homozygous	59172830
4	208515943	208515944	A	G	11	GENIC	homozygous	57066616
4	208517244	208517245	A	C	16	GENIC	homozygous	59172832
4	208519509	208519510	G	GT	6	GENIC	heterozygous	58704313
4	208519902	208519903	T	C	6	GENIC	homozygous	58600907
4	208522353	208522354	T	C	18	GENIC	possibly homozygous	57066620
4	208523079	208523080	A	G	19	GENIC	homozygous	57066621
4	208529860	208529861	G	C	23	GENIC	homozygous	57066623
4	208533095	208533096	G	A	19	GENIC	homozygous	57066627
4	208533489	208533490	T	C	22	GENIC	homozygous	58600923