chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	53990059	53990060	A	G	47	GENIC	homozygous	67997600
8	53990475	53990476	C	T	46	GENIC	homozygous	67997603
8	53990902	53990903	T	C	30	GENIC	homozygous	68733184
8	53991879	53991880	G	C	41	GENIC	homozygous	67997606
8	53992003	53992004	T	A	25	GENIC	homozygous	67997610
8	53992200	53992201	T	C	43	GENIC	homozygous	67997613
8	53992342	53992343	A	G	22	GENIC	heterozygous	67997616
8	53993606	53993607	A	G	50	GENIC	homozygous	67997620
8	53994209	53994210	C	T	15	GENIC	homozygous	67997624
8	53994754	53994755	T	C	34	GENIC	homozygous	67997627
8	53999593	53999594	A	C	58	GENIC	homozygous	67997630
8	54000303	54000304	C	T	9	GENIC	homozygous	67997633
8	54000305	54000306	G	A	9	GENIC	homozygous	67997636
8	54000316	54000317	T	C	9	GENIC	homozygous	67997639
8	54000332	54000333	C	G	10	GENIC	homozygous	67997642
8	54000342	54000343	C	A	13	GENIC	homozygous	67997645
8	54000365	54000366	G	T	15	GENIC	homozygous	67997648
8	54000393	54000394	T	C	21	GENIC	homozygous	67997652
8	54000852	54000853	C	T	17	GENIC	heterozygous	67997655
8	54001817	54001818	G	A	25	GENIC	homozygous	67997658
8	54001927	54001928	G	T	50	GENIC	homozygous	67997661
8	54002783	54002784	C	G	59	GENIC	homozygous	67997665
8	54003924	54003925	T	A	39	GENIC	homozygous	67997669
8	54006565	54006566	C	T	15	GENIC	possibly homozygous	67997672
8	54006567	54006568	C	T	15	GENIC	possibly homozygous	67997675
8	54006595	54006596	C	T	15	GENIC	heterozygous	67997680
8	54008168	54008169	A	T	50	GENIC	homozygous	67997683
8	54008457	54008458	A	C	25	GENIC	heterozygous	67997686
8	54008863	54008864	G	A	43	GENIC	homozygous	67997689
8	54009873	54009874	A	T	20	GENIC	heterozygous	67997692
8	54010012	54010013	G	A	49	GENIC	homozygous	67997695