chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	15108736	15108737	C	CCCTCTT	29	GENIC	homozygous	51624090
10	15109043	15109044	T	G	22	GENIC	homozygous	52835264
10	15109046	15109047	G	-	20	GENIC	homozygous	52113112
10	15109602	15109603	A	AATT	11	GENIC	homozygous	52113114
10	15109605	15109606	C	CGAA	12	GENIC	homozygous	52113116
10	15109608	15109611	TTC	---	13	GENIC	homozygous	52113118
10	15109614	15109616	AA	--	12	GENIC	homozygous	52113120
10	15109621	15109622	A	C	12	GENIC	homozygous	52113122
10	15109624	15109625	T	C	12	GENIC	homozygous	52113124
10	15110644	15110645	A	C	22	GENIC	homozygous	51624093
10	15111093	15111094	C	T	38	GENIC	homozygous	52113126
10	15113611	15113612	C	T	20	GENIC	homozygous	52113130
10	15116099	15116100	G	GAAAAAA	13	GENIC	homozygous	51330906
10	15116340	15116341	G	A	31	GENIC	homozygous	52113132
10	15116504	15116505	G	GCT	12	GENIC	homozygous	51624098
10	15117058	15117059	C	-	9	GENIC	homozygous	51624099
10	15117817	15117818	G	A	12	GENIC	homozygous	52113134
10	15118567	15118568	G	C	18	GENIC	homozygous	51624102