chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	81969806	81969807	G	A	28	GENIC	homozygous	113277088
4	81969941	81969942	T	C	31	GENIC	homozygous	113037162
4	81970741	81970742	T	C	31	GENIC	homozygous	113277089
4	81971181	81971182	A	G	17	GENIC	homozygous	113037164
4	81973713	81973714	C	T	19	GENIC	homozygous	113277091
4	81976355	81976356	T	C	37	GENIC	homozygous	112749788
4	81976702	81976703	G	A	33	GENIC	homozygous	113277092
4	81978597	81978598	G	A	32	GENIC	homozygous	112749792
4	81979964	81979965	A	G	29	GENIC	homozygous	112749798
4	81981247	81981248	C	T	16	GENIC	homozygous	113277093
4	81986331	81986332	A	G	29	GENIC	homozygous	112749802
4	81987641	81987642	T	C	22	GENIC	homozygous	112749804
4	81991262	81991263	A	G	27	GENIC	homozygous	112749806
4	81992034	81992035	G	A	31	GENIC	homozygous	113037181
4	81985168	81985169	A	T	30	GENIC	homozygous	113461455
4	81995128	81995129	A	G	32	GENIC	possibly homozygous	112749820
4	82003419	82003420	C	G	17	GENIC	homozygous	113277095
4	82003636	82003637	A	G	27	GENIC	homozygous	112749836
4	82004149	82004150	A	G	17	GENIC	homozygous	112749840
4	82004989	82004990	G	A	32	GENIC	homozygous	113277096
4	82005181	82005182	G	C	26	GENIC	homozygous	112749842
4	82006640	82006641	T	A	10	GENIC	homozygous	119434977
4	82008239	82008240	A	G	19	GENIC	homozygous	112749844
4	82009640	82009641	C	T	27	GENIC	homozygous	112749848
4	82010144	82010145	A	G	18	GENIC	homozygous	112749850
4	82011167	82011168	C	T	28	GENIC	homozygous	112749852
4	82011372	82011373	C	G	38	GENIC	homozygous	112749854
4	82011516	82011517	T	C	22	GENIC	homozygous	112749856