chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	133995812	133995813	T	C	60	GENIC	homozygous	71151434
4	133995934	133995935	G	A	42	GENIC	homozygous	71151437
4	133995982	133995983	C	T	31	GENIC	homozygous	71151440
4	133996073	133996074	T	C	48	GENIC	homozygous	71151443
4	133996166	133996167	A	G	60	GENIC	homozygous	71151447
4	133996323	133996324	C	T	53	GENIC	homozygous	71151450
4	133996575	133996576	G	A	43	GENIC	possibly homozygous	71151454
4	133996637	133996638	T	C	59	GENIC	possibly homozygous	71151457
4	133997177	133997178	A	C	28	GENIC	homozygous	71151458
4	133997365	133997366	C	T	48	GENIC	homozygous	71151461
4	133997369	133997370	C	T	51	GENIC	homozygous	71151464
4	133997750	133997751	T	G	42	GENIC	homozygous	71151467
4	133997922	133997923	C	T	45	GENIC	homozygous	71151470
4	133998138	133998139	C	A	38	GENIC	homozygous	71151473
4	133998188	133998189	A	T	30	GENIC	homozygous	71151476
4	133998461	133998462	T	C	45	GENIC	possibly homozygous	71151479
4	133998609	133998610	T	C	49	GENIC	possibly homozygous	71151482
4	133998646	133998647	C	T	47	GENIC	homozygous	71151485
4	133998648	133998649	G	A	50	GENIC	homozygous	71151488
4	133998681	133998682	G	A	54	GENIC	homozygous	71151491
4	133998692	133998693	T	C	49	GENIC	homozygous	71151494
4	133998742	133998743	G	C	53	GENIC	homozygous	71151497
4	133998750	133998751	C	A	63	GENIC	homozygous	71151500
4	133998818	133998819	A	G	50	GENIC	possibly homozygous	71151503
4	133998917	133998918	A	C	44	GENIC	possibly homozygous	71151506
4	133998994	133998995	T	C	49	GENIC	homozygous	71151509
4	133999440	133999441	C	T	33	GENIC	homozygous	71151512