chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	212655812	212655813	G	A	1	GENIC	homozygous	61076553
1	212658705	212658706	G	A	16	GENIC	possibly homozygous	61076554
1	212659762	212659763	T	G	19	GENIC	possibly homozygous	61076555
1	212659968	212659969	A	AT	3	GENIC	heterozygous	61076556
1	212661571	212661572	G	T	12	GENIC	possibly homozygous	61076557
1	212663465	212663466	C	T	24	GENIC	homozygous	61076562
1	212664831	212664832	C	T	14	GENIC	homozygous	61076563
1	212666283	212666284	A	G	12	GENIC	homozygous	61076564
1	212666736	212666737	C	CAG	3	GENIC	homozygous	61076565
1	212669279	212669280	T	C	14	GENIC	homozygous	61076566
1	212669743	212669744	A	G	20	GENIC	homozygous	61076569
1	212670030	212670031	A	G	31	GENIC	possibly homozygous	61076570
1	212670346	212670347	C	G	23	GENIC	homozygous	61076571
1	212671116	212671117	C	T	25	GENIC	homozygous	61076572
1	212674420	212674421	G	A	27	GENIC	possibly homozygous	61076573
1	212674751	212674752	T	-	12	GENIC	homozygous	61076574
1	212676526	212676527	G	A	12	GENIC	heterozygous	61076575
1	212680462	212680463	C	T	19	GENIC	homozygous	61076577
1	212685080	212685081	G	A	26	GENIC	heterozygous	61076578
1	212688791	212688792	T	C	26	GENIC	possibly homozygous	61076579