chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	18081805	18081805		C	42	GENIC	homozygous	132143653
10	18082372	18082372		C	41	GENIC	homozygous	132143654
10	18082352	18082352		G	39	GENIC	homozygous	131463887
10	18083723	18083723		A	47	GENIC	homozygous	132143655
10	18085424	18085424		CAAACT	51	GENIC	homozygous	128792555
10	18082578	18082578		TAACCTAGG	65	GENIC	homozygous	128792552
10	18084706	18084707	G	A	46	GENIC	homozygous	116740410
10	18085543	18085543		A	48	GENIC	homozygous	128792556
10	18085578	18085579	G		49	GENIC	homozygous	128792557
10	18085583	18085583		A	49	GENIC	homozygous	128792558
10	18085587	18085588	A		48	GENIC	homozygous	128792559
10	18085593	18085593		A	47	GENIC	homozygous	128792560
10	18086007	18086008	T	C	40	GENIC	homozygous	116502037
10	18086139	18086140	G	A	52	GENIC	homozygous	116740411
10	18086437	18086438	G	A	37	GENIC	homozygous	116740412
10	18086908	18086909	A	G	39	GENIC	homozygous	116502047
10	18087117	18087119	AC		47	GENIC	homozygous	128792565
10	18087564	18087565	C	T	49	GENIC	homozygous	116502063
10	18087564	18087564		A	48	GENIC	homozygous	128792566
10	18087744	18087745	G	T	49	GENIC	homozygous	116740413
10	18087974	18087975	T		48	GENIC	homozygous	128792567
10	18088241	18088242	A	G	50	GENIC	homozygous	116740414
10	18087795	18087796	T	C	46	GENIC	homozygous	116502071
10	18090466	18090467	A	G	40	GENIC	homozygous	116740415