chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	61594772	61594773	C	T	12	GENIC	homozygous	143889497
3	61595378	61595379	G	T	10	GENIC	homozygous	141514331
3	61595792	61595793	T	C	10	GENIC	homozygous	141514332
3	61597893	61597894	G	A	13	GENIC	homozygous	141514333
3	61598428	61598429	G	A	16	GENIC	homozygous	143889498
3	61599065	61599066	G	A	7	GENIC	homozygous	141514334
3	61599362	61599366	ACAT		12	GENIC	homozygous	141476179
3	61602296	61602298	TA		8	GENIC	heterozygous	141476180
3	61597250	61597255	TTTTG		14	GENIC	homozygous	141476176
3	61598043	61598043		AT	17	GENIC	homozygous	141476178
3	61599062	61599062		TTTA	7	GENIC	homozygous	143856837
3	61602360	61602360		TG	16	GENIC	possibly homozygous	141476181
3	61602959	61602960	C	T	19	GENIC	homozygous	141514336
3	61602301	61602302	G		8	GENIC	heterozygous	403066033
3	61602301	61602302	G	A	8	GENIC	heterozygous	403066034