chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	86013971	86013971		GCTC	27	GENIC	homozygous	142790344
1	86016497	86016498	G	A	44	GENIC	homozygous	142842988
1	86017273	86017274	G	A	28	GENIC	homozygous	142842989
1	86017324	86017325	A	G	31	GENIC	homozygous	142842990
1	86018080	86018081	T	C	38	GENIC	homozygous	142842991
1	86019798	86019799	C	T	44	GENIC	homozygous	142842992
1	86020047	86020048	G	A	50	GENIC	homozygous	142842993
1	86020261	86020267	CAGAAG		50	GENIC	homozygous	142790345
1	86021287	86021288	G	A	51	GENIC	homozygous	142842994
1	86022789	86022790	A	G	36	GENIC	homozygous	142842995
1	86022844	86022845	A	G	37	GENIC	homozygous	142842996
1	86022913	86022914	A	G	32	GENIC	homozygous	142842997
1	86023712	86023713	T	A	34	GENIC	homozygous	142842998
1	86023808	86023861	CACTGAGCCACGCCCCCAGCCCCTCACTGGGGGATTCTAGGCAGGGGCTCTAT		32	GENIC	homozygous	142790346
1	86024403	86024404	C	T	12	GENIC	homozygous	142842999
1	86024803	86024804	T	C	21	GENIC	homozygous	142843000
1	86025786	86025787	G	A	43	GENIC	homozygous	142843001
1	86025958	86025959	T	C	46	GENIC	homozygous	142843002
1	86026419	86026420	T	G	46	GENIC	homozygous	142843003
1	86026956	86026958	TA		37	GENIC	homozygous	142790347
1	86027840	86027841	G	A	57	GENIC	homozygous	142843004
1	86027992	86027993	T	A	47	GENIC	homozygous	142843005
1	86029079	86029080	C	T	38	GENIC	possibly homozygous	142843006
1	86018300	86018301	T		15	GENIC	heterozygous	402951696
1	86018300	86018301	T	C	15	GENIC	heterozygous	402951697
1	86029342	86029343	G	A	35	GENIC	homozygous	142843007
1	86030282	86030283	G	C	42	GENIC	homozygous	142843008
1	86031092	86031093	A	G	33	GENIC	homozygous	142843009