chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	70622843	70622844	A	C	36	GENIC	homozygous	53392560
8	70623003	70623004	T	G	45	GENIC	homozygous	53392561
8	70623282	70623283	G	-	44	GENIC	homozygous	53966356
8	70624061	70624062	T	G	41	GENIC	homozygous	53392563
8	70625669	70625673	ATGT	----	23	GENIC	homozygous	53966358
8	70625798	70625799	A	ATG	30	GENIC	possibly homozygous	53124995
8	70625821	70625822	C	T	38	GENIC	homozygous	53392567
8	70626164	70626165	T	G	49	GENIC	homozygous	53392568
8	70626457	70626458	T	C	30	GENIC	homozygous	53966360
8	70626587	70626588	C	T	33	GENIC	homozygous	53966362
8	70627264	70627265	C	A	47	GENIC	homozygous	53966364
8	70627561	70627562	A	C	27	GENIC	homozygous	53966366
8	70628469	70628470	G	A	37	GENIC	homozygous	53966368
8	70628591	70628592	A	G	47	GENIC	homozygous	53966370
8	70629310	70629312	TG	--	31	GENIC	possibly homozygous	53966372
8	70629975	70629976	A	-	14	GENIC	homozygous	53966374
8	70630149	70630150	G	C	40	GENIC	homozygous	53966376
8	70630268	70630279	GGTCGTAGCTA	-----------	64	GENIC	homozygous	53966378
8	70625817	70625818	C	T	39	GENIC	homozygous	52673389