chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	56042579	56042580	A	G	39	GENIC	homozygous	110542764
18	56042624	56042625	T	G	38	GENIC	possibly homozygous	110542766
18	56042732	56042733	G	A	40	GENIC	homozygous	110542768
18	56043716	56043717	A	G	54	GENIC	homozygous	110542770
18	56043833	56043834	T	C	57	GENIC	homozygous	110542772
18	56043863	56043864	T	C	57	GENIC	homozygous	110542774
18	56043959	56043960	G	A	47	GENIC	homozygous	110542776
18	56043965	56043966	C	G	43	GENIC	homozygous	110542778
18	56044916	56044917	C	A	66	GENIC	homozygous	110592626
18	56045047	56045048	A	G	52	GENIC	homozygous	110592628
18	56045140	56045141	A	C	48	GENIC	homozygous	110542780
18	56046112	56046113	G	A	40	GENIC	homozygous	110542782
18	56046119	56046120	G	C	40	GENIC	possibly homozygous	110542784
18	56046227	56046228	A	G	49	GENIC	homozygous	110542786
18	56046546	56046547	G	A	39	GENIC	homozygous	110542792
18	56046613	56046614	C	T	55	GENIC	possibly homozygous	110592630
18	56046637	56046638	C	T	60	GENIC	homozygous	110875808
18	56046939	56046940	C	T	58	GENIC	homozygous	110542794
18	56047121	56047122	A	T	55	GENIC	possibly homozygous	110542796