chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	81817040	81817041	A	G	14	GENIC	possibly homozygous	52267522
9	81817135	81817136	G	A	20	GENIC	possibly homozygous	52267524
9	81817524	81817525	T	A	22	GENIC	homozygous	52267528
9	81818987	81818988	G	A	16	GENIC	possibly homozygous	52267530
9	81819267	81819268	G	C	2	GENIC	homozygous	52267534
9	81819746	81819747	A	C	2	GENIC	homozygous	52267536
9	81820089	81820090	C	CCCT	2	GENIC	homozygous	52267538
9	81820320	81820321	G	GC	19	GENIC	possibly homozygous	52267542
9	81821638	81821639	T	C	16	GENIC	possibly homozygous	52267544
9	81821711	81821712	G	-	9	GENIC	homozygous	52267546
9	81822264	81822265	A	G	25	GENIC	possibly homozygous	52267548
9	81823733	81823734	C	T	13	GENIC	possibly homozygous	52267556
9	81824415	81824416	A	C	13	GENIC	heterozygous	52267558
9	81824862	81824863	A	G	13	GENIC	homozygous	52267560
9	81824967	81824968	T	C	14	GENIC	possibly homozygous	52267562
9	81825517	81825518	T	TTCGC	5	GENIC	homozygous	52267564
9	81826137	81826138	G	C	2	GENIC	homozygous	52267566
9	81826694	81826695	G	T	28	GENIC	homozygous	52267570
9	81827725	81827726	T	A	15	GENIC	possibly homozygous	52267573
9	81827819	81827820	A	G	16	GENIC	possibly homozygous	52267575
9	81828023	81828024	T	A	12	GENIC	homozygous	52267577
9	81828059	81828060	T	A	5	GENIC	heterozygous	52267579
9	81828979	81828980	G	A	11	GENIC	homozygous	52267581