chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	33743046	33743047	G	A	40	GENIC	homozygous	113265710
4	33743115	33743116	A	G	40	GENIC	homozygous	113265714
4	33743135	33743136	A	G	48	GENIC	homozygous	113265715
4	33744070	33744071	G	A	37	GENIC	homozygous	113097856
4	33744875	33744876	T	C	56	GENIC	homozygous	113097858
4	33745044	33745045	A	C	34	GENIC	homozygous	113097860
4	33745386	33745387	G	C	29	GENIC	possibly homozygous	113265716
4	33745486	33745487	G	A	42	GENIC	possibly homozygous	113265717
4	33749192	33749193	T	C	63	GENIC	homozygous	113265718
4	33749315	33749316	C	T	67	GENIC	homozygous	113265719
4	33749756	33749757	G	A	71	GENIC	homozygous	113265720
4	33750964	33750965	G	A	50	GENIC	homozygous	113265721
4	33751633	33751634	A	G	38	GENIC	homozygous	113265722
4	33752649	33752650	T	C	64	GENIC	homozygous	113097905
4	33753570	33753571	G	A	56	GENIC	possibly homozygous	113097925
4	33754865	33754867	AT		56	GENIC	homozygous	130928073
4	33756275	33756276	C	T	57	GENIC	homozygous	113265723
4	33756609	33756610	T	A	46	GENIC	homozygous	113265724
4	33759055	33759056	G	A	48	GENIC	homozygous	113265725
4	33759318	33759319	G	T	47	GENIC	homozygous	113265726
4	33759976	33759977	T	A	47	GENIC	possibly homozygous	113265727
4	33760337	33760338	G	A	26	GENIC	homozygous	113265728