chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	111233484	111233485	A	G	20	GENIC	homozygous	117623918
9	111233646	111233647	G	C	33	GENIC	homozygous	117623920
9	111234470	111234471	G	A	19	GENIC	homozygous	117623922
9	111235761	111235762	G	A	18	GENIC	homozygous	117623924
9	111235900	111235901	G	A	12	GENIC	homozygous	117623926
9	111237810	111237811	C	T	29	GENIC	possibly homozygous	117623930
9	111238608	111238609	T	C	31	GENIC	homozygous	117623932
9	111238844	111238845	C	T	26	GENIC	homozygous	117623934
9	111239217	111239218	A	G	29	GENIC	homozygous	117623936
9	111240580	111240581	T	C	21	GENIC	homozygous	117623938
9	111240847	111240848	C	T	24	GENIC	homozygous	117623940
9	111241782	111241783	C	T	31	GENIC	homozygous	117623942
9	111242025	111242026	A	T	23	GENIC	homozygous	117623944
9	111242643	111242644	G	A	28	GENIC	homozygous	117623946
9	111245809	111245810	C	T	35	GENIC	homozygous	117623950
9	111245941	111245942	C	G	23	GENIC	homozygous	117623952
9	111246335	111246336	T	C	30	GENIC	homozygous	117623954
9	111247122	111247123	C	G	4	GENIC	homozygous	120405849
9	111247123	111247124	T	G	3	GENIC	homozygous	120405850