chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	18082578	18082578		TAACCTAGG	37	GENIC	homozygous	128792552
10	18083718	18083719	G	A	38	GENIC	homozygous	116918516
10	18084628	18084629	T	C	47	GENIC	homozygous	116918518
10	18084680	18084681	A	C	52	GENIC	homozygous	116918520
10	18085424	18085424		CAAACT	49	GENIC	homozygous	128792555
10	18085543	18085543		A	37	GENIC	homozygous	128792556
10	18085578	18085579	G		34	GENIC	homozygous	128792557
10	18085583	18085583		A	36	GENIC	homozygous	128792558
10	18085587	18085588	A		32	GENIC	homozygous	128792559
10	18085593	18085593		A	30	GENIC	homozygous	128792560
10	18086007	18086008	T	C	36	GENIC	homozygous	116502037
10	18086822	18086823	C	T	39	GENIC	homozygous	116918522
10	18086908	18086909	A	G	32	GENIC	homozygous	116502047
10	18087117	18087119	AC		37	GENIC	homozygous	128792565
10	18087314	18087315	A	C	24	GENIC	homozygous	116918524
10	18087564	18087565	C	T	28	GENIC	homozygous	116502063
10	18087564	18087564		A	28	GENIC	homozygous	128792566
10	18087795	18087796	T	C	46	GENIC	homozygous	116502071
10	18087974	18087975	T		28	GENIC	homozygous	128792567
10	18089383	18089384	G	A	47	GENIC	homozygous	116918526
10	18090466	18090467	A	G	38	GENIC	homozygous	116740415
10	18086381	18086382	C	T	29	GENIC	homozygous	118063517