chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	52149452	52149453	G	T	47	GENIC	homozygous	119547230
4	52149830	52149831	A		45	GENIC	homozygous	128034411
4	52150662	52150662		ATCT	24	GENIC	homozygous	134932735
4	52151104	52151105	G	A	39	GENIC	homozygous	119547232
4	52153123	52153124	A	C	37	GENIC	homozygous	112650865
4	52153778	52153779	C	T	47	GENIC	homozygous	113445942
4	52156356	52156357	T	C	42	GENIC	homozygous	112650871
4	52157505	52157506	G	A	37	GENIC	homozygous	112650873
4	52157915	52157916	T	C	51	GENIC	homozygous	112650875
4	52158143	52158144	T		45	GENIC	possibly homozygous	134932736
4	52159202	52159203	G	C	38	GENIC	homozygous	113445946
4	52159741	52159742	G	A	43	GENIC	homozygous	112650876
4	52163194	52163194		A	50	GENIC	homozygous	128034415
4	52163996	52163996		A	10	GENIC	homozygous	134932737
4	52163998	52163998		GAA	10	GENIC	homozygous	134932738
4	52163996	52163997	C	A	10	GENIC	homozygous	134934332
4	52165026	52165027	A	G	38	GENIC	homozygous	112650881
4	52165111	52165112	G	T	35	GENIC	homozygous	112650883
4	52166214	52166215	G	A	32	GENIC	homozygous	113445950
4	52165085	52165096	AGAGGAGGTGA		38	GENIC	homozygous	134932739
4	52165827	52165827		T	18	GENIC	homozygous	128034418