chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	264060117	264060118	A	G	32	GENIC	homozygous	108634996
1	264060439	264060440	A	G	40	GENIC	homozygous	109217699
1	264061026	264061027	A	G	34	GENIC	homozygous	109217701
1	264061283	264061284	G	A	36	GENIC	homozygous	109217703
1	264061466	264061467	T	C	22	GENIC	homozygous	108635000
1	264062297	264062298	T	C	24	GENIC	homozygous	108635006
1	264062501	264062502	A	G	27	GENIC	homozygous	108635009
1	264062532	264062533	C	T	32	GENIC	homozygous	109217705
1	264062601	264062602	C	T	28	GENIC	homozygous	109217707
1	264062947	264062948	G	A	44	GENIC	homozygous	109217709
1	264064003	264064004	A	G	22	GENIC	homozygous	108635013
1	264064234	264064235	T	G	20	GENIC	homozygous	108635015
1	264064641	264064642	C	T	35	GENIC	homozygous	108635017
1	264064988	264064989	A	G	41	GENIC	homozygous	108635019
1	264065091	264065092	T	C	31	GENIC	homozygous	108635021
1	264065234	264065235	G	A	49	GENIC	heterozygous	108635023
1	264065424	264065425	C	A	29	GENIC	homozygous	109217711
1	264065813	264065814	A	T	47	GENIC	possibly homozygous	109217713
1	264066698	264066699	T	C	32	GENIC	homozygous	108635024
1	264066832	264066833	G	A	19	GENIC	homozygous	109217715
1	264066841	264066842	C	T	22	GENIC	homozygous	109217717
1	264067060	264067061	T	C	24	GENIC	homozygous	108635026
1	264067293	264067294	A	G	21	GENIC	homozygous	108635028
1	264067967	264067968	C	T	38	GENIC	possibly homozygous	109217719
1	264068063	264068064	T	C	34	GENIC	homozygous	108635030
1	264069621	264069622	C	T	24	GENIC	homozygous	109217721
1	264069737	264069738	C	T	34	GENIC	homozygous	109217723
1	264069747	264069748	G	A	31	GENIC	homozygous	109217725
1	264070790	264070791	C	T	54	GENIC	possibly homozygous	108782985
1	264071386	264071387	G	A	29	GENIC	homozygous	108635036
1	264071462	264071463	C	A	33	GENIC	homozygous	109217727