chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94164947	94164948	A	G	53	GENIC	homozygous	117604745
9	94165093	94165094	C	T	39	GENIC	homozygous	117601827
9	94166481	94166482	C	T	40	GENIC	homozygous	117604747
9	94166782	94166783	G	A	59	GENIC	homozygous	117604749
9	94168028	94168029	C	T	56	GENIC	homozygous	117601831
9	94168501	94168502	A	G	57	GENIC	homozygous	117604753
9	94169110	94169111	G	A	48	GENIC	homozygous	117601833
9	94169530	94169531	G	T	54	GENIC	homozygous	117601835
9	94170173	94170174	A	G	45	GENIC	homozygous	117601837
9	94171634	94171635	A	T	25	GENIC	homozygous	117601839
9	94172166	94172167	T	C	39	GENIC	homozygous	117604759
9	94172185	94172186	T	C	36	GENIC	homozygous	117604761
9	94172840	94172841	A	G	36	GENIC	possibly homozygous	117601841
9	94165828	94165835	GACGAGC		36	GENIC	homozygous	132135222
9	94169335	94169335		A	42	GENIC	homozygous	128733174
9	94175746	94175747	A	G	38	GENIC	homozygous	117601845
9	94176108	94176109	A	G	36	GENIC	homozygous	117604769
9	94176715	94176716	T	A	40	GENIC	homozygous	117601847
9	94178237	94178240	TGC		38	GENIC	homozygous	132135223
9	94179202	94179206	AAAC		50	GENIC	homozygous	128733176
9	94179998	94179999	C	T	32	GENIC	homozygous	117601849
9	94180005	94180006	T	A	30	GENIC	homozygous	117601851
9	94180109	94180110	A	G	40	GENIC	homozygous	117390000
9	94180113	94180114	C	A	40	GENIC	homozygous	117390002
9	94180908	94180909	G	A	44	GENIC	homozygous	117601853
9	94181116	94181117	C	T	59	GENIC	possibly homozygous	117601855
9	94181443	94181444	A	G	51	GENIC	homozygous	117390003
9	94181615	94181615		TACA	49	GENIC	homozygous	131894203
9	94183022	94183023	T	C	42	GENIC	homozygous	117604775
9	94183237	94183238	G	A	43	GENIC	homozygous	117604777
9	94183975	94183975		C	33	GENIC	possibly homozygous	132135224
9	94184045	94184046	G	A	40	GENIC	homozygous	117601859
9	94184764	94184765	A	G	48	GENIC	homozygous	117604781
9	94184900	94184901	G	A	50	GENIC	homozygous	117604783