chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	47519693	47519696	TCC	---	29	GENIC	homozygous	59802333
2	47520263	47520264	C	A	25	GENIC	homozygous	59802334
2	47520274	47520275	T	A	21	GENIC	homozygous	58799296
2	47520355	47520356	T	TCAGTCCC	3	GENIC	homozygous	59681325
2	47520387	47520388	G	-	8	GENIC	possibly homozygous	58799297
2	47520400	47520401	G	-	17	GENIC	heterozygous	58799298
2	47520407	47520408	C	-	17	GENIC	heterozygous	58799299
2	47520412	47520413	C	-	18	GENIC	heterozygous	58799300
2	47520918	47520919	T	A	32	GENIC	homozygous	59802335
2	47521198	47521199	A	G	33	GENIC	homozygous	59681335
2	47521338	47521339	C	T	20	GENIC	homozygous	58799301
2	47521372	47521374	AC	--	12	GENIC	homozygous	59802336
2	47521453	47521454	C	T	38	GENIC	homozygous	59802337
2	47521970	47521971	A	G	23	GENIC	homozygous	59681343
2	47522034	47522035	T	C	23	GENIC	homozygous	59802338
2	47523633	47523634	T	TAAG	14	GENIC	homozygous	59681353
2	47524050	47524051	A	AGTT	19	GENIC	homozygous	59681359
2	47524239	47524240	G	C	22	GENIC	homozygous	59802339