chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	87296742	87296743	C	CT	26	INTERGENIC	homozygous	51529880
10	87300114	87300115	C	CAT	29	INTERGENIC	homozygous	51529890
10	87300385	87300389	GTGT	----	12	INTERGENIC	heterozygous	52392899
10	87300387	87300389	GT	--	12	INTERGENIC	heterozygous	52392901
10	87301172	87301173	A	AGT	8	INTERGENIC	homozygous	51529903
10	87301259	87301267	GTGTGTGT	--------	2	INTERGENIC	homozygous	52392903
10	87303606	87303607	A	G	20	INTERGENIC	homozygous	51726269
10	87303656	87303657	A	G	21	INTERGENIC	homozygous	51529914
10	87303894	87303895	T	-	22	INTERGENIC	homozygous	51529917
10	87304227	87304228	A	ATCTG	25	INTERGENIC	homozygous	51529918
10	87304417	87304418	C	T	23	INTERGENIC	homozygous	51726271
10	87305523	87305524	T	C	14	INTERGENIC	homozygous	51529919
10	87305625	87305626	T	C	21	INTERGENIC	homozygous	51529920
10	87305629	87305630	G	A	20	INTERGENIC	homozygous	51529921
10	87306287	87306288	A	ACTGGGCTGGCAGCAG	12	GENIC	homozygous	52392905
10	87297708	87297709	A	AT	32	INTERGENIC	possibly homozygous	51923688
10	87302414	87302415	T	A	19	INTERGENIC	homozygous	51923690