chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	172120454	172120455	T	C	48	GENIC	homozygous	112953399
4	172120643	172120644	A	T	62	GENIC	homozygous	112953401
4	172120677	172120678	C	T	68	GENIC	homozygous	112953403
4	172120690	172120691	A	C	67	GENIC	homozygous	112953405
4	172120855	172120856	C	T	51	GENIC	homozygous	112953407
4	172121462	172121463	A	G	54	GENIC	homozygous	112953409
4	172122430	172122431	A	T	46	GENIC	homozygous	112953411
4	172122629	172122630	G	A	27	GENIC	homozygous	112953413
4	172124453	172124454	A	G	57	GENIC	homozygous	112953419
4	172123725	172123726	A		36	GENIC	homozygous	128105069
4	172125995	172125999	TCTT		47	GENIC	possibly homozygous	128105070
4	172128819	172128820	A	G	48	GENIC	homozygous	112953423
4	172130602	172130603	A	G	68	GENIC	homozygous	112953425
4	172131858	172131859	C	T	46	GENIC	homozygous	112953427
4	172132125	172132126	A	G	57	GENIC	homozygous	112953429
4	172132384	172132385	T	C	55	GENIC	homozygous	112953431
4	172132443	172132444	A	G	56	GENIC	homozygous	112953433
4	172133471	172133472	G	C	36	GENIC	homozygous	112953441
4	172132590	172132591	A	G	50	GENIC	homozygous	112953435
4	172132812	172132813	T	G	48	GENIC	homozygous	112953437
4	172133314	172133315	T	C	57	GENIC	homozygous	112953439
4	172133533	172133534	G	A	30	GENIC	homozygous	113067984
4	172133559	172133560	G	A	32	GENIC	homozygous	112953443
4	172133697	172133698	A	G	43	GENIC	homozygous	112953445
4	172133779	172133780	T	G	40	GENIC	homozygous	112953447
4	172133983	172133984	T	C	42	GENIC	homozygous	112953449
4	172134034	172134035	C	T	41	GENIC	homozygous	112953451