chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	61595378	61595379	G	T	19	GENIC	homozygous	141514331
3	61595792	61595793	T	C	23	GENIC	homozygous	141514332
3	61597250	61597255	TTTTG		10	GENIC	homozygous	141476176
3	61597893	61597894	G	A	29	GENIC	homozygous	141514333
3	61597989	61597997	TATGTATA		25	GENIC	homozygous	141476177
3	61598043	61598043		AT	26	GENIC	homozygous	141476178
3	61599065	61599066	G	A	7	GENIC	homozygous	141514334
3	61599362	61599366	ACAT		16	GENIC	homozygous	141476179
3	61600340	61600341	C	T	17	GENIC	homozygous	141514335
3	61602296	61602298	TA		15	GENIC	homozygous	141476180
3	61602301	61602302	G		17	GENIC	heterozygous	403066033
3	61602301	61602302	G	A	17	GENIC	homozygous	403066034
3	61602360	61602360		TG	16	GENIC	homozygous	141476181
3	61602959	61602960	C	T	21	GENIC	homozygous	141514336
3	61603127	61603128	C	T	24	GENIC	homozygous	141514337
3	61603578	61603579	A		19	GENIC	homozygous	141476182
3	61604082	61604083	A	C	16	GENIC	homozygous	141514338
3	61604150	61604151	T	C	9	GENIC	homozygous	141514339