chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	56338147	56338148	C	T	20	GENIC	homozygous	110543188
18	56338803	56338804	T	C	27	GENIC	heterozygous	119495659
18	56341738	56341739	C	T	47	GENIC	homozygous	110361422
18	56341849	56341850	G	C	45	GENIC	homozygous	110361424
18	56345026	56345027	A	G	38	GENIC	homozygous	110361464
18	56345648	56345649	C	T	32	GENIC	homozygous	110543190
18	56345990	56345991	G	A	37	GENIC	homozygous	110543192
18	56347522	56347523	G	A	34	GENIC	possibly homozygous	110543194
18	56347933	56347934	C	G	44	GENIC	homozygous	110543196
18	56348309	56348310	A	C	46	GENIC	homozygous	110361486
18	56349012	56349013	C	G	49	GENIC	homozygous	110543198
18	56350340	56350341	A	C	57	GENIC	possibly homozygous	110361490
18	56351653	56351654	A	C	152	GENIC	heterozygous	110921347
18	56355232	56355233	T	G	16	GENIC	homozygous	110361500
18	56355273	56355274	T	C	18	GENIC	homozygous	110361502
18	56355277	56355278	T	G	19	GENIC	homozygous	110361504
18	56355315	56355316	T	A	21	GENIC	homozygous	110361506