chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	15405125	15405126	A	G	7	INTERGENIC	homozygous	52337977
9	15405209	15405210	T	C	12	INTERGENIC	homozygous	52337978
9	15405218	15405219	T	C	12	INTERGENIC	homozygous	52337979
9	15405505	15405506	A	G	7	INTERGENIC	homozygous	51767303
9	15405530	15405531	C	G	9	INTERGENIC	homozygous	52337980
9	15405587	15405588	A	G	9	INTERGENIC	homozygous	52337981
9	15405588	15405589	G	C	9	INTERGENIC	homozygous	52337982
9	15405675	15405676	G	GTTGGAAATCT	15	INTERGENIC	homozygous	52899290
9	15405833	15405834	T	-	10	INTERGENIC	homozygous	52337983
9	15405971	15405972	C	A	18	INTERGENIC	homozygous	52337984
9	15406113	15406114	A	G	7	INTERGENIC	homozygous	52337985
9	15406163	15406164	A	G	9	INTERGENIC	homozygous	52337986
9	15407438	15407439	T	C	11	INTERGENIC	homozygous	51767307
9	15408175	15408176	T	C	9	INTERGENIC	homozygous	51767309
9	15408503	15408504	A	T	15	INTERGENIC	homozygous	52337987
9	15408824	15408825	G	A	19	INTERGENIC	homozygous	52337988
9	15408961	15408962	T	C	11	INTERGENIC	homozygous	51767311
9	15408972	15408973	G	A	12	INTERGENIC	homozygous	52337989
9	15410674	15410675	C	A	10	INTERGENIC	homozygous	51767313
9	15410730	15410731	C	T	9	INTERGENIC	homozygous	51767315
9	15410879	15410880	G	A	17	INTERGENIC	homozygous	51767317