chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	75633311	75633312	C	T	30	GENIC	homozygous	116800574
10	75633995	75633996	T	C	27	GENIC	homozygous	116639545
10	75634324	75634325	A	G	37	GENIC	homozygous	116639547
10	75635131	75635132	T	C	27	GENIC	homozygous	116639555
10	75635240	75635241	T	C	29	GENIC	homozygous	116639559
10	75635431	75635432	T	C	29	GENIC	homozygous	116639563
10	75635852	75635853	G	A	32	GENIC	homozygous	116800576
10	75636011	75636012	C	T	42	GENIC	homozygous	116800578
10	75636628	75636629	T	A	36	GENIC	homozygous	116639571
10	75638994	75638995	T	C	45	GENIC	homozygous	116639591
10	75639011	75639012	A	C	48	GENIC	homozygous	116639593
10	75639714	75639715	A	G	35	GENIC	possibly homozygous	116639595
10	75640732	75640733	G	A	39	GENIC	homozygous	116800580
10	75641335	75641336	T	C	42	GENIC	homozygous	116800582
10	75642731	75642732	A	C	36	GENIC	homozygous	116639621
10	75642859	75642860	A	G	48	GENIC	homozygous	116800584
10	75642987	75642988	T	C	34	GENIC	homozygous	116639623