chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94164947	94164948	A	G	25	GENIC	homozygous	117389976
9	94165093	94165094	C	T	21	GENIC	homozygous	117601827
9	94166481	94166482	C	T	33	GENIC	possibly homozygous	117389977
9	94166782	94166783	G	A	22	GENIC	homozygous	117389979
9	94168028	94168029	C	T	25	GENIC	homozygous	117601831
9	94168501	94168502	A	G	18	GENIC	homozygous	117389982
9	94169110	94169111	G	A	20	GENIC	homozygous	117601833
9	94169530	94169531	G	T	18	GENIC	homozygous	117601835
9	94170173	94170174	A	G	35	GENIC	homozygous	117601837
9	94172166	94172167	T	C	22	GENIC	homozygous	117389986
9	94172185	94172186	T	C	19	GENIC	homozygous	117389988
9	94172840	94172841	A	G	20	GENIC	homozygous	117601841
9	94175746	94175747	A	G	22	GENIC	homozygous	117601845
9	94176108	94176109	A	G	24	GENIC	homozygous	117389995
9	94176715	94176716	T	A	20	GENIC	homozygous	117601847
9	94179998	94179999	C	T	27	GENIC	homozygous	117601849
9	94180005	94180006	T	A	25	GENIC	homozygous	117601851
9	94180109	94180110	A	G	13	GENIC	homozygous	117390000
9	94181116	94181117	C	T	18	GENIC	homozygous	117601855
9	94183022	94183023	T	C	40	GENIC	homozygous	117390005
9	94183237	94183238	G	A	33	GENIC	homozygous	117390006
9	94184045	94184046	G	A	22	GENIC	homozygous	117601859
9	94184764	94184765	A	G	16	GENIC	homozygous	117390011
9	94184900	94184901	G	A	28	GENIC	homozygous	117390012