chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	45509829	45509830	C	T	45	GENIC	possibly homozygous	52617279
8	45509833	45509834	A	T	43	GENIC	possibly homozygous	52617281
8	45509888	45509889	T	C	36	GENIC	homozygous	52617283
8	45509943	45509944	C	T	45	GENIC	homozygous	52617285
8	45509946	45509947	G	A	44	GENIC	homozygous	52617287
8	45510028	45510029	T	TG	40	GENIC	homozygous	52617289
8	45510165	45510166	G	A	58	GENIC	homozygous	52617291
8	45510246	45510247	G	C	60	GENIC	homozygous	52617293
8	45510473	45510474	A	T	67	GENIC	possibly homozygous	52617295
8	45510584	45510585	C	T	46	GENIC	homozygous	52617297
8	45510881	45510882	C	T	57	GENIC	homozygous	52617299
8	45510903	45510904	C	T	51	GENIC	possibly homozygous	52617301
8	45511457	45511458	T	C	52	GENIC	homozygous	52617303
8	45511467	45511468	G	A	49	GENIC	homozygous	52617305
8	45511517	45511518	T	C	47	GENIC	homozygous	52617307
8	45511675	45511676	A	G	47	GENIC	homozygous	52617309
8	45511780	45511781	A	G	47	GENIC	homozygous	52617311
8	45511802	45511803	G	-	42	GENIC	homozygous	52617313
8	45511818	45511819	T	C	57	GENIC	possibly homozygous	52617315