chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	439037	439038	A	G	71	GENIC	homozygous	112461501
4	439997	439998	G	A	42	GENIC	homozygous	112461506
4	440067	440068	T	C	46	GENIC	homozygous	112461508
4	441461	441462	T	A	62	GENIC	homozygous	112461513
4	441720	441721	A	C	40	GENIC	homozygous	112461515
4	442042	442043	A	G	53	GENIC	homozygous	112461518
4	442253	442254	C	T	44	GENIC	possibly homozygous	112461520
4	443454	443455	G	A	43	GENIC	possibly homozygous	112461522
4	443893	443894	C	A	50	GENIC	homozygous	112461524
4	444321	444322	C	T	45	GENIC	homozygous	112461527
4	444341	444342	C	T	47	GENIC	homozygous	112461529
4	444498	444499	C	T	28	GENIC	homozygous	112461532
4	439845	439845		ACGAAAACG	39	GENIC	homozygous	127998127
4	440568	440569	T		45	GENIC	homozygous	127998128
4	442879	442880	A		33	GENIC	homozygous	127998129
4	443092	443097	TTTCT		32	GENIC	homozygous	127998130