chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	15087032	15087033	T	A	12	GENIC	homozygous	58086170
3	15087442	15087443	C	T	9	GENIC	homozygous	58086172
3	15087902	15087903	G	A	16	GENIC	homozygous	58086174
3	15088074	15088075	C	A	17	GENIC	homozygous	58086176
3	15088527	15088528	G	-	13	GENIC	homozygous	58086178
3	15089759	15089760	T	C	12	GENIC	homozygous	58086184
3	15089954	15089955	G	A	10	GENIC	homozygous	58086186
3	15090107	15090108	A	G	10	GENIC	homozygous	58086188
3	15091160	15091161	T	C	8	GENIC	homozygous	58086190
3	15091848	15091849	A	C	9	GENIC	homozygous	58086194
3	15092256	15092257	G	A	8	GENIC	homozygous	58086196
3	15093626	15093627	T	C	12	GENIC	homozygous	58086207
3	15093712	15093713	T	C	8	GENIC	homozygous	58086209
3	15093822	15093823	A	G	8	GENIC	homozygous	58086213
3	15093945	15093946	A	G	10	GENIC	homozygous	58086215
3	15094013	15094015	TT	--	9	GENIC	homozygous	58086217
3	15094192	15094193	G	A	7	GENIC	homozygous	58086220
3	15094389	15094390	A	G	9	GENIC	homozygous	58086222
3	15095505	15095506	T	C	11	GENIC	homozygous	58086234
3	15096574	15096575	C	T	14	GENIC	homozygous	58086236
3	15097434	15097435	T	C	8	GENIC	homozygous	58086240
3	15097467	15097468	A	G	11	GENIC	homozygous	58086242
3	15097857	15097858	G	T	16	GENIC	homozygous	58086244