chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	82387321	82387322	G	A	51	GENIC	homozygous	55504305
5	82387948	82387949	A	C	51	GENIC	homozygous	55504308
5	82387965	82387966	C	T	43	GENIC	homozygous	55504311
5	82388194	82388195	G	A	36	GENIC	homozygous	55504314
5	82388282	82388283	C	CT	24	GENIC	possibly homozygous	55504317
5	82388974	82388975	A	G	45	GENIC	homozygous	55504319
5	82389097	82389098	C	T	62	GENIC	possibly homozygous	55504322
5	82389466	82389467	G	C	38	GENIC	homozygous	55504325
5	82390450	82390451	G	A	29	GENIC	homozygous	55504328
5	82390852	82390853	A	T	39	GENIC	homozygous	55504330
5	82391232	82391233	C	T	58	GENIC	homozygous	55504333
5	82392357	82392358	C	T	35	GENIC	homozygous	55504336
5	82392541	82392542	T	A	53	GENIC	homozygous	55504339
5	82392607	82392608	C	T	43	GENIC	homozygous	55504342
5	82393210	82393211	A	G	42	GENIC	homozygous	55504344
5	82393769	82393770	G	A	27	GENIC	homozygous	55504346
5	82393825	82393826	C	A	29	GENIC	homozygous	55504349
5	82394447	82394448	G	A	49	GENIC	homozygous	55504352
5	82394809	82394810	A	T	28	GENIC	homozygous	55504355
5	82395542	82395543	C	T	40	GENIC	homozygous	55504358
5	82395975	82395976	G	A	19	GENIC	homozygous	55504361
5	82396748	82396749	A	G	38	GENIC	homozygous	55504364
5	82397663	82397664	A	G	56	GENIC	homozygous	55504367
5	82397943	82397944	A	G	40	GENIC	homozygous	55504369
5	82398224	82398225	T	TAAG	19	GENIC	heterozygous	55504372
5	82398247	82398251	CTCT	----	16	GENIC	homozygous	55504375
5	82399509	82399510	C	T	37	GENIC	homozygous	55504378