chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	141409397	141409398	A	G	61	GENIC	possibly homozygous	112168396
3	141411385	141411385		GG	14	GENIC	homozygous	131328522
3	141412144	141412145	A	G	37	GENIC	homozygous	112168398
3	141412837	141412838	A	G	50	GENIC	homozygous	112168400
3	141412845	141412846	T	C	48	GENIC	homozygous	112168402
3	141413449	141413450	T	C	47	GENIC	homozygous	112168404
3	141414977	141414978	G	C	20	GENIC	homozygous	111755862
3	141412970	141412971	G	T	50	GENIC	homozygous	111755858
3	141414527	141414528	A	T	55	GENIC	homozygous	111755860
3	141415817	141415818	A	C	59	GENIC	homozygous	111755870
3	141415885	141415886	C		55	GENIC	homozygous	130912257
3	141415887	141415888	C	T	55	GENIC	homozygous	119685726
3	141416385	141416385		TTTCTTTC	46	GENIC	homozygous	130912258
3	141417767	141417768	A	G	56	GENIC	homozygous	112168406
3	141418301	141418302	C	A	60	GENIC	possibly homozygous	112168408
3	141418683	141418684	A	C	41	GENIC	homozygous	111755874