chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	47829439	47829440	G	A	42	GENIC	homozygous	141206793
1	47829555	47829556	T	C	39	GENIC	homozygous	141206794
1	47829720	47829721	A	G	38	GENIC	homozygous	141206795
1	47829848	47829849	A	G	44	GENIC	homozygous	141206796
1	47829874	47829875	T	C	48	GENIC	homozygous	141206797
1	47830122	47830123	G	A	42	GENIC	homozygous	141206798
1	47830447	47830448	A	G	44	GENIC	homozygous	141206799
1	47831045	47831046	C	T	46	GENIC	homozygous	141206800
1	47831079	47831080	A	G	53	GENIC	homozygous	141206801
1	47831124	47831125	C	G	53	GENIC	homozygous	141206802
1	47831499	47831500	C	T	48	GENIC	homozygous	141206803
1	47831624	47831624		AG	48	GENIC	homozygous	141160768
1	47832352	47832354	AA		25	GENIC	homozygous	141160769
1	47832382	47832386	TATA		22	GENIC	homozygous	141160770
1	47833113	47833114	T	C	47	GENIC	homozygous	141206804
1	47833395	47833396	G	T	47	GENIC	homozygous	141206805
1	47833500	47833501	A	G	39	GENIC	homozygous	141206806
1	47833536	47833537	G	C	46	GENIC	homozygous	141206807
1	47833833	47833834	A	T	40	GENIC	homozygous	141206808
1	47833944	47833945	G	A	34	GENIC	homozygous	141206809
1	47834035	47834041	TTAACG		40	GENIC	homozygous	141160771
1	47834139	47834140	A	T	44	GENIC	homozygous	141206810
1	47834214	47834215	C	T	40	GENIC	homozygous	141206811
1	47834267	47834272	CTTCA		41	GENIC	homozygous	141160772
1	47835028	47835029	T	C	43	GENIC	homozygous	141206812
1	47835255	47835256	T		39	GENIC	homozygous	141160773
1	47836164	47836165	A	G	46	GENIC	homozygous	141206813
1	47836514	47836515	C	T	48	GENIC	homozygous	141206814
1	47836572	47836573	C	G	55	GENIC	homozygous	141206815
1	47835990	47835991	A	C	16	GENIC	homozygous	145259197