chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	56338147	56338148	C	T	66	GENIC	homozygous	110543188
18	56341738	56341739	C	T	29	GENIC	homozygous	110361422
18	56341849	56341850	G	C	49	GENIC	homozygous	110361424
18	56345026	56345027	A	G	41	GENIC	homozygous	110361464
18	56345648	56345649	C	T	42	GENIC	homozygous	110543190
18	56345990	56345991	G	A	30	GENIC	homozygous	110543192
18	56347522	56347523	G	A	56	GENIC	homozygous	110543194
18	56347933	56347934	C	G	33	GENIC	homozygous	110543196
18	56348309	56348310	A	C	44	GENIC	homozygous	110361486
18	56349012	56349013	C	G	57	GENIC	homozygous	110543198
18	56350340	56350341	A	C	32	GENIC	homozygous	110361490
18	56355232	56355233	T	G	43	GENIC	homozygous	110361500
18	56355273	56355274	T	C	49	GENIC	homozygous	110361502
18	56355277	56355278	T	G	48	GENIC	homozygous	110361504
18	56355315	56355316	T	A	50	GENIC	homozygous	110361506
18	56355342	56355343	C	G	34	GENIC	homozygous	110631238
18	56355344	56355345	T	G	28	GENIC	homozygous	110631240
18	56355348	56355349	T	G	26	GENIC	homozygous	110631242
18	56355355	56355356	T	C	27	GENIC	homozygous	110631244
18	56355359	56355360	T	G	27	GENIC	homozygous	110631246