chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	94098719	94098720	G	A	55	GENIC	homozygous	141218921
1	94098778	94098778		ATCCATCCATCC	38	GENIC	homozygous	141163326
1	94098836	94098836		ATCC	48	GENIC	homozygous	141163327
1	94099407	94099408	G	T	58	GENIC	homozygous	141218922
1	94099486	94099487	T	C	52	GENIC	homozygous	141218923
1	94099759	94099760	C	G	50	GENIC	homozygous	141218924
1	94100062	94100063	A	G	50	GENIC	homozygous	141218925
1	94100100	94100101	A	G	47	GENIC	homozygous	141218926
1	94100386	94100387	T	C	32	GENIC	homozygous	141218927
1	94100718	94100719	T	A	53	GENIC	homozygous	141218928
1	94100719	94100720	T	G	53	GENIC	homozygous	141218929
1	94101181	94101181		G	51	GENIC	homozygous	141163328
1	94101276	94101277	G	T	52	GENIC	homozygous	141218932
1	94100914	94100915	T	C	51	GENIC	homozygous	141218930
1	94101255	94101256	A	G	57	GENIC	homozygous	141218931
1	94101538	94101539	C	T	43	GENIC	homozygous	141218933
1	94101546	94101547	A	G	48	GENIC	homozygous	141218934
1	94101566	94101567	G		48	GENIC	homozygous	141163329
1	94101713	94101714	A	G	46	GENIC	homozygous	141218935
1	94101777	94101778	T	C	48	GENIC	homozygous	141218936
1	94101778	94101779	G	A	48	GENIC	homozygous	141218937
1	94101856	94101857	C	T	39	GENIC	homozygous	141218938
1	94102520	94102521	C	T	53	GENIC	homozygous	141218939
1	94102758	94102759	A	G	47	GENIC	possibly homozygous	141218940