chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	212655812	212655813	G	A	6	GENIC	homozygous	61076553
1	212658705	212658706	G	A	29	GENIC	homozygous	61076554
1	212659762	212659763	T	G	27	GENIC	homozygous	61076555
1	212659968	212659969	A	AT	22	GENIC	possibly homozygous	61076556
1	212661571	212661572	G	T	38	GENIC	homozygous	61076557
1	212662522	212662523	A	ATT	17	GENIC	possibly homozygous	61076558
1	212662522	212662523	A	AT	17	GENIC	heterozygous	62275082
1	212662934	212662935	T	-	20	GENIC	homozygous	61076559
1	212663465	212663466	C	T	17	GENIC	homozygous	61076562
1	212664831	212664832	C	T	32	GENIC	homozygous	61076563
1	212666283	212666284	A	G	35	GENIC	homozygous	61076564
1	212666736	212666737	C	CAG	16	GENIC	possibly homozygous	61076565
1	212669279	212669280	T	C	23	GENIC	homozygous	61076566
1	212669743	212669744	A	G	31	GENIC	homozygous	61076569
1	212670030	212670031	A	G	27	GENIC	homozygous	61076570
1	212670346	212670347	C	G	37	GENIC	homozygous	61076571
1	212671116	212671117	C	T	22	GENIC	homozygous	61076572
1	212671289	212671290	C	CTT	11	GENIC	heterozygous	62196064
1	212671289	212671290	C	CTTTT	11	GENIC	heterozygous	62196066
1	212674420	212674421	G	A	26	GENIC	homozygous	61076573
1	212674751	212674752	T	-	20	GENIC	homozygous	61076574
1	212676526	212676527	G	A	29	GENIC	homozygous	61076575
1	212676698	212676699	G	GTTGT	27	GENIC	homozygous	61076576
1	212678348	212678351	AGG	---	27	GENIC	heterozygous	62248739
1	212680462	212680463	C	T	33	GENIC	homozygous	61076577
1	212681105	212681229	AAAAACACGTGAGTCCGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	----------------------------------------------------------------------------------------------------------------------------	23	GENIC	homozygous	62098775
1	212685080	212685081	G	A	37	GENIC	homozygous	61076578
1	212688791	212688792	T	C	34	GENIC	homozygous	61076579