chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	85859457	85859458	G	A	12	GENIC	possibly homozygous	49021347
14	85859907	85859908	G	A	5	GENIC	heterozygous	49525605
14	85860123	85860124	A	G	1	GENIC	homozygous	49525607
14	85860361	85860362	C	CCTT	1	GENIC	homozygous	49525609
14	85861167	85861168	A	G	5	GENIC	heterozygous	49525614
14	85861334	85861335	G	T	4	GENIC	heterozygous	49525616
14	85861571	85861572	T	C	13	GENIC	heterozygous	49525618
14	85861689	85861690	A	G	17	GENIC	possibly homozygous	49525620
14	85861748	85861749	C	T	12	GENIC	homozygous	49525622
14	85862397	85862398	C	T	11	GENIC	possibly homozygous	49525626
14	85862582	85862583	G	A	14	GENIC	homozygous	49525628
14	85863773	85863774	T	G	3	GENIC	heterozygous	49525630
14	85864166	85864167	G	-	7	GENIC	homozygous	49525632
14	85864204	85864205	A	G	10	GENIC	possibly homozygous	49525634
14	85864552	85864553	A	T	18	GENIC	homozygous	49525636
14	85864969	85864970	G	A	16	GENIC	possibly homozygous	49525638
14	85865542	85865544	TG	--	2	GENIC	homozygous	49525642
14	85865634	85865635	A	C	17	GENIC	possibly homozygous	49525644
14	85866474	85866475	A	G	8	GENIC	homozygous	49021368
14	85866908	85866909	A	C	15	GENIC	homozygous	49525650
14	85867477	85867478	G	A	11	GENIC	homozygous	49525652
14	85867568	85867569	A	G	9	GENIC	possibly homozygous	49021371
14	85868130	85868131	G	A	18	GENIC	possibly homozygous	49525654