chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	82595325	82595326	C	CA	5	GENIC	homozygous	62137450
1	82595346	82595347	A	G	12	GENIC	homozygous	61669581
1	82595611	82595612	T	TGTCTGTGTC	18	GENIC	homozygous	62137451
1	82595737	82595738	G	A	26	GENIC	possibly homozygous	61450171
1	82596094	82596095	C	T	19	GENIC	homozygous	61669583
1	82596122	82596123	G	GGCTCTACCACTGAGCCACGCCCCCAGCCCCTCACTGGGGGATTCTAGGCAGGGAGGA	5	GENIC	homozygous	62137452
1	82596974	82596975	G	A	23	GENIC	possibly homozygous	61450174
1	82597350	82597351	C	CGG	6	GENIC	homozygous	61669585
1	82597444	82597445	C	CCCCAGTGAGGGATTGGGGATGTGGCCCAGTGGTAGAGCCCCTGCCTAGAACCT	17	GENIC	homozygous	62137453
1	82599041	82599044	TTT	---	4	GENIC	heterozygous	61450178
1	82599042	82599044	TT	--	4	GENIC	heterozygous	61450179
1	82600087	82600088	T	A	27	GENIC	homozygous	61450181
1	82601688	82601689	C	T	21	GENIC	homozygous	61669586
1	82603490	82603491	C	T	14	INTERGENIC	homozygous	61669587
1	82603622	82603623	A	G	15	INTERGENIC	homozygous	61450184
1	82603711	82603712	G	A	25	INTERGENIC	possibly homozygous	61450185
1	82603761	82603762	G	A	25	INTERGENIC	possibly homozygous	61450186
1	82605589	82605590	G	A	27	INTERGENIC	homozygous	61450188
1	82606541	82606542	A	G	22	INTERGENIC	homozygous	61669588
1	82606830	82606831	T	G	34	INTERGENIC	possibly homozygous	61669589
1	82607048	82607049	G	A	28	INTERGENIC	possibly homozygous	61669590
1	82607257	82607258	C	CA	4	INTERGENIC	heterozygous	62137454
1	82607257	82607258	C	CAAA	4	INTERGENIC	heterozygous	62137455
1	82607995	82607996	C	T	28	INTERGENIC	homozygous	61669591
1	82608361	82608362	G	A	25	INTERGENIC	homozygous	61669592