chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	15533462	15533463	C	T	51	GENIC	homozygous	110282344
18	15534521	15534522	T	C	44	GENIC	homozygous	110282346
18	15534578	15534579	T	C	64	GENIC	homozygous	110282348
18	15535193	15535194	C	T	50	GENIC	possibly homozygous	110282351
18	15535402	15535403	T	G	45	GENIC	homozygous	110282353
18	15535693	15535694	T	C	52	GENIC	homozygous	110282355
18	15536041	15536042	G	A	57	GENIC	homozygous	110282357
18	15537320	15537321	T	G	43	GENIC	homozygous	110282359
18	15538208	15538209	T	C	58	GENIC	homozygous	110282361
18	15540168	15540169	C	T	61	GENIC	possibly homozygous	110282363
18	15540570	15540571	T	A	58	GENIC	homozygous	110282365
18	15540710	15540711	T	C	63	GENIC	homozygous	110282367
18	15541320	15541321	A	G	43	GENIC	homozygous	110282369
18	15541328	15541329	C	T	44	GENIC	homozygous	110282371
18	15541840	15541841	C	T	57	GENIC	homozygous	110282373
18	15542029	15542030	G	A	59	GENIC	homozygous	110282375
18	15539653	15539654	C	T	55	GENIC	heterozygous	119482686
18	15539633	15539634	T	A	49	GENIC	heterozygous	119578447