chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157660034	157660035	G	T	37	GENIC	homozygous	112906818
4	157660036	157660037	G	T	37	GENIC	homozygous	119282475
4	157660041	157660042	G	T	35	GENIC	homozygous	119282477
4	157666698	157666699	T	C	27	GENIC	homozygous	112906820
4	157668604	157668605	T	G	42	GENIC	homozygous	112906822
4	157668837	157668838	G	A	41	GENIC	homozygous	112906824
4	157668971	157668972	C	G	48	GENIC	homozygous	112906826
4	157669281	157669282	C	T	33	GENIC	homozygous	112906828
4	157669365	157669366	G	A	36	GENIC	homozygous	112906832
4	157669875	157669876	A	G	34	GENIC	homozygous	112906838
4	157670107	157670108	C	T	32	GENIC	homozygous	112906840
4	157670110	157670111	T	C	31	GENIC	homozygous	112906842
4	157670141	157670142	T	C	31	GENIC	homozygous	112906844
4	157670348	157670349	A	G	27	GENIC	homozygous	113062919
4	157670355	157670356	G	T	28	GENIC	homozygous	112906850
4	157670656	157670657	C	T	19	GENIC	homozygous	112906852
4	157671018	157671019	C	T	45	GENIC	homozygous	112906854
4	157671641	157671642	A	G	21	GENIC	homozygous	112906858
4	157672472	157672473	A	G	36	GENIC	homozygous	112906860
4	157672720	157672721	T	C	35	GENIC	homozygous	112906862
4	157672742	157672743	A	G	34	GENIC	homozygous	112906864
4	157673257	157673258	C	T	46	GENIC	homozygous	112906878
4	157673392	157673393	C	T	25	GENIC	homozygous	112906880
4	157673433	157673434	G	T	28	GENIC	homozygous	112906882
4	157674036	157674037	C	G	5	GENIC	heterozygous	119467008
4	157674810	157674811	T	C	17	GENIC	homozygous	112906888