chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	81796337	81796338	A	ACTG	7	GENIC	homozygous	53723328
9	81796911	81796912	A	T	12	GENIC	homozygous	52761585
9	81797634	81797635	T	C	7	GENIC	homozygous	52761588
9	81800612	81800613	T	C	7	GENIC	homozygous	52267454
9	81801412	81801413	C	T	7	GENIC	homozygous	53723330
9	81801768	81801769	C	T	11	GENIC	homozygous	52761598
9	81802000	81802001	C	-	11	GENIC	homozygous	52761600
9	81802278	81802279	C	T	16	GENIC	homozygous	53723332
9	81803679	81803680	T	C	7	GENIC	homozygous	52761606
9	81803692	81803693	T	G	10	GENIC	homozygous	52267464
9	81804082	81804084	TG	--	11	GENIC	homozygous	52027556
9	81804096	81804097	T	TAC	11	GENIC	homozygous	52952818
9	81804269	81804270	A	G	12	GENIC	homozygous	52267470
9	81804295	81804298	AGA	---	10	GENIC	homozygous	52761608
9	81805879	81805880	A	T	12	GENIC	homozygous	52267480
9	81806719	81806720	T	C	14	GENIC	homozygous	52761611
9	81807232	81807233	T	G	14	GENIC	homozygous	52267486
9	81809391	81809392	G	A	9	GENIC	homozygous	52761617