chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	82053725	82053726	T	TTC	18	GENIC	heterozygous	52268565
9	82053853	82053854	A	C	6	GENIC	homozygous	52913502
9	82053857	82053858	A	T	3	GENIC	heterozygous	52913503
9	82053894	82053895	C	-	6	GENIC	heterozygous	52027718
9	82053906	82053907	A	T	8	GENIC	homozygous	52027720
9	82054035	82054038	CAT	---	8	GENIC	homozygous	52268571
9	82054097	82054098	T	-	7	GENIC	homozygous	52913504
9	82054876	82054879	CAT	---	7	GENIC	homozygous	52027722
9	82056278	82056279	A	G	37	GENIC	homozygous	52268573
9	82056448	82056450	AC	--	15	GENIC	homozygous	52913505
9	82056999	82057000	A	T	17	GENIC	possibly homozygous	52268577
9	82057035	82057036	G	A	22	GENIC	possibly homozygous	52268579
9	82057330	82057331	A	G	30	GENIC	homozygous	52268581
9	82058789	82058791	CA	--	17	GENIC	homozygous	52268583
9	82058995	82058996	C	T	30	GENIC	homozygous	52268585
9	82058724	82058725	G	-	13	GENIC	homozygous	52762480
9	82053894	82053895	C	CCT	6	GENIC	heterozygous	52952988
9	82056989	82056990	A	C	13	GENIC	heterozygous	53641144
9	82059667	82059668	G	T	23	GENIC	possibly homozygous	52268587
9	82060168	82060171	CTC	---	14	GENIC	homozygous	52268589
9	82060614	82060615	A	T	30	GENIC	possibly homozygous	52268591
9	82060677	82060678	T	C	26	GENIC	possibly homozygous	52268593
9	82061555	82061556	T	C	22	GENIC	homozygous	52268595
9	82061701	82061702	G	A	29	GENIC	possibly homozygous	52268597
9	82061969	82061970	G	A	23	GENIC	homozygous	52268599
9	82062963	82062964	T	C	27	GENIC	homozygous	52268601
9	82063631	82063632	G	A	18	GENIC	possibly homozygous	52268603
9	82063633	82063634	C	-	17	GENIC	homozygous	52268605
9	82064599	82064600	C	-	26	GENIC	homozygous	52268607
9	82065015	82065016	T	C	21	GENIC	possibly homozygous	52268609
9	82065148	82065150	GT	--	10	GENIC	homozygous	52952992
9	82065844	82065845	T	C	26	GENIC	homozygous	52268615