chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	111235345	111235346	C	T	31	GENIC	homozygous	117741092
9	111235761	111235762	G	A	20	GENIC	homozygous	117623924
9	111235900	111235901	G	A	21	GENIC	homozygous	117623926
9	111236098	111236099	G	T	13	GENIC	heterozygous	120398173
9	111237810	111237811	C	T	30	GENIC	homozygous	117623930
9	111238608	111238609	T	C	33	GENIC	homozygous	117623932
9	111238844	111238845	C	T	35	GENIC	homozygous	117623934
9	111238925	111238926	T	C	40	GENIC	homozygous	117741094
9	111240580	111240581	T	C	32	GENIC	homozygous	117623938
9	111239217	111239218	A	G	37	GENIC	homozygous	117623936
9	111241584	111241585	T	C	39	GENIC	homozygous	117741098
9	111241782	111241783	C	T	31	GENIC	homozygous	117623942
9	111241982	111241983	A	G	52	GENIC	homozygous	117741100
9	111242643	111242644	G	A	34	GENIC	homozygous	117623946
9	111245775	111245776	C	T	22	GENIC	homozygous	117741102
9	111245941	111245942	C	G	20	GENIC	homozygous	117623952
9	111246335	111246336	T	C	23	GENIC	homozygous	117623954