chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	53990059	53990060	A	G	24	GENIC	possibly homozygous	67997600
8	53990475	53990476	C	T	20	GENIC	homozygous	67997603
8	53991879	53991880	G	C	16	GENIC	homozygous	67997606
8	53992003	53992004	T	A	30	GENIC	homozygous	67997610
8	53992200	53992201	T	C	26	GENIC	homozygous	67997613
8	53993606	53993607	A	G	17	GENIC	homozygous	67997620
8	53994209	53994210	C	T	18	GENIC	homozygous	67997624
8	53994754	53994755	T	C	24	GENIC	possibly homozygous	67997627
8	53999593	53999594	A	C	28	GENIC	homozygous	67997630
8	54000826	54000827	C	T	9	GENIC	homozygous	69398562
8	54000827	54000828	T	C	8	GENIC	homozygous	69398563
8	54001817	54001818	G	A	26	GENIC	homozygous	67997658
8	54002783	54002784	C	G	22	GENIC	homozygous	67997665
8	54003924	54003925	T	A	16	GENIC	homozygous	67997669
8	53994890	53994891	C	G	29	GENIC	homozygous	69277694
8	54008168	54008169	A	T	23	GENIC	homozygous	67997683
8	54008457	54008458	A	C	16	GENIC	possibly homozygous	67997686
8	54008863	54008864	G	A	29	GENIC	homozygous	67997689
8	54009873	54009874	A	T	15	GENIC	homozygous	67997692
8	54010012	54010013	G	A	20	GENIC	homozygous	67997695