chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	123664768	123664769	G	A	7	GENIC	homozygous	112825545
4	123664940	123664941	G	T	25	GENIC	homozygous	112825547
4	123665032	123665033	A	G	29	GENIC	homozygous	112825549
4	123666435	123666436	A	T	39	GENIC	homozygous	112825551
4	123666575	123666576	A	G	28	GENIC	homozygous	112825553
4	123666710	123666711	C	G	5	GENIC	homozygous	112825555
4	123666924	123666925	C	T	37	GENIC	homozygous	112825559
4	123667042	123667043	T	G	36	GENIC	possibly homozygous	112825561
4	123667054	123667055	G	T	32	GENIC	possibly homozygous	112825563
4	123667500	123667501	A	G	26	GENIC	possibly homozygous	112825565
4	123667696	123667697	G	C	32	GENIC	homozygous	112825567
4	123672779	123672780	C	T	71	GENIC	heterozygous	113049406
4	123672785	123672786	G	A	70	GENIC	heterozygous	113049408
4	123672786	123672787	G	A	70	GENIC	heterozygous	113049410
4	123695655	123695656	C	A	40	GENIC	homozygous	112825569
4	123695662	123695663	C	A	42	GENIC	homozygous	112825571
4	123695667	123695668	C	A	45	GENIC	homozygous	112825573
4	123672769	123672770	G	T	73	GENIC	heterozygous	113299676