chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157727037	157727038	T	C	69	GENIC	homozygous	112906942
4	157727272	157727273	T	C	58	GENIC	homozygous	112906944
4	157727860	157727861	G		35	GENIC	homozygous	128096241
4	157727865	157727867	CT		35	GENIC	homozygous	128096242
4	157727894	157727895	G		20	GENIC	homozygous	128096243
4	157727924	157727925	A		12	GENIC	homozygous	128096244
4	157727940	157727943	CTC		6	GENIC	homozygous	131364172
4	157727951	157727952	C	G	9	GENIC	homozygous	113062923
4	157727970	157727973	CCT		8	GENIC	homozygous	128096245
4	157728000	157728003	GCT		9	GENIC	homozygous	128096246
4	157728008	157728026	CTCCTTCCCTCCCTCCTT		9	GENIC	homozygous	128096247
4	157728080	157728081	T	C	25	GENIC	homozygous	112906946
4	157728952	157728953	T	C	58	GENIC	homozygous	112906948
4	157729285	157729286	A	G	65	GENIC	homozygous	112906950
4	157729645	157729646	A	G	53	GENIC	homozygous	112906952
4	157730362	157730363	G	T	44	GENIC	homozygous	113400752
4	157730529	157730529		CTTTA	37	GENIC	homozygous	128096248
4	157732248	157732249	C	T	42	GENIC	homozygous	112906954