chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	56068881	56068882	A	G	50	GENIC	homozygous	137474821
5	56068919	56068921	GG		43	GENIC	possibly homozygous	137309704
5	56069015	56069016	C	T	39	GENIC	possibly homozygous	137474822
5	56069313	56069314	G	T	45	GENIC	homozygous	137474823
5	56069445	56069445		A	41	GENIC	possibly homozygous	137309705
5	56069468	56069469	C	T	48	GENIC	homozygous	137474824
5	56069825	56069826	T	A	41	GENIC	homozygous	137474826
5	56070156	56070157	T		32	GENIC	homozygous	137309706
5	56070941	56070942	G	A	32	GENIC	homozygous	137474827
5	56071353	56071354	T	C	64	GENIC	homozygous	137474828
5	56071694	56071695	C	A	51	GENIC	homozygous	137474829
5	56071756	56071757	T	C	49	GENIC	homozygous	137474830
5	56072137	56072138	C	T	59	GENIC	homozygous	137474831
5	56072450	56072451	T	C	52	GENIC	homozygous	137474832
5	56072818	56072819	T	C	57	GENIC	homozygous	137474835
5	56073088	56073089	T	C	55	GENIC	homozygous	141726701
5	56073360	56073361	C	A	69	GENIC	homozygous	141726702
5	56073365	56073366	C	T	67	GENIC	homozygous	141726703
5	56073782	56073783	C	T	62	GENIC	homozygous	141726704
5	56073882	56073883	C	T	64	GENIC	homozygous	137474838
5	56074191	56074192	A		50	GENIC	homozygous	141682347
5	56075718	56075719	C	T	54	GENIC	homozygous	141726705
5	56076561	56076562	T	C	60	GENIC	homozygous	137474839
5	56078670	56078670		A	35	GENIC	homozygous	141682348