chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	54089401	54089402	G	C	67	GENIC	homozygous	142072565
8	54089408	54089409	T	C	64	GENIC	homozygous	142072566
8	54090194	54090195	A	G	58	GENIC	homozygous	138334997
8	54090658	54090659	G	A	60	GENIC	homozygous	138334998
8	54091085	54091086	T		43	GENIC	possibly homozygous	141014848
8	54091759	54091760	A	G	48	GENIC	homozygous	138334999
8	54095166	54095167	C	T	55	GENIC	homozygous	142072567
8	54095279	54095280	A	C	32	GENIC	homozygous	142072568
8	54095970	54095971	T		54	GENIC	homozygous	142024226
8	54094512	54094513	G		53	GENIC	homozygous	138246073
8	54095638	54095642	TGAA		34	GENIC	homozygous	138246074
8	54093537	54093537		TGAATGAA	39	GENIC	homozygous	142024224
8	54095968	54095969	T		53	GENIC	homozygous	142024225
8	54095345	54095346	A	G	11	GENIC	heterozygous	403726725
8	54095341	54095342	A		11	GENIC	possibly homozygous	403238376
8	54095341	54095342	A	G	11	GENIC	heterozygous	403238377
8	54095345	54095346	A		11	GENIC	possibly homozygous	403726724
8	54095347	54095348	A		11	GENIC	possibly homozygous	403726726
8	54095347	54095348	A	G	11	GENIC	heterozygous	403726727
8	54098075	54098076	A	T	42	GENIC	homozygous	142072569
8	54098654	54098655	G	T	68	GENIC	homozygous	142072570
8	54098680	54098681	T	G	71	GENIC	homozygous	142072571
8	54099726	54099727	A	G	41	GENIC	homozygous	142072572
8	54100339	54100340	C	G	48	GENIC	homozygous	138335001
8	54100659	54100660	A	G	44	GENIC	homozygous	138335002
8	54100695	54100696	C	A	46	GENIC	homozygous	142072573
8	54103944	54103945	A	G	60	GENIC	homozygous	142072574
8	54104643	54104644	C	T	53	GENIC	homozygous	142072575