chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157127932	157127933	C	T	14	GENIC	homozygous	112905477
4	157128941	157128942	T	G	9	GENIC	homozygous	112905479
4	157129150	157129151	A	G	16	GENIC	homozygous	112905481
4	157129153	157129154	G	C	17	GENIC	homozygous	112905483
4	157129293	157129294	T	G	13	GENIC	homozygous	112905485
4	157130255	157130256	A	G	18	GENIC	homozygous	112905487
4	157130261	157130261		TATAGGTCTAGAATAGCTCCCC	17	GENIC	homozygous	128096027
4	157130302	157130303	G	A	13	GENIC	homozygous	112905489
4	157130649	157130650	C	G	9	GENIC	homozygous	112905491
4	157131094	157131095	T	A	13	GENIC	homozygous	112905493
4	157132353	157132354	A	G	16	GENIC	homozygous	112905495
4	157132776	157132777	T	G	12	GENIC	homozygous	112905497
4	157133713	157133714	C	T	18	GENIC	homozygous	112905499
4	157133758	157133759	C	T	16	GENIC	homozygous	112905501
4	157134281	157134282	T	A	14	GENIC	homozygous	112905507
4	157134353	157134354	T	C	11	GENIC	homozygous	112905509
4	157134471	157134472	A	T	13	GENIC	homozygous	112905511
4	157134715	157134716	G	A	12	GENIC	homozygous	112905513