chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	163756634	163756635	C	G	40	GENIC	homozygous	135733896
1	163757746	163757747	G	A	36	GENIC	homozygous	135733897
1	163757954	163757962	TCACGGAA		45	GENIC	homozygous	135441962
1	163764271	163764272	T	C	41	GENIC	homozygous	135733898
1	163766024	163766028	TGTG		47	GENIC	homozygous	135441963
1	163766030	163766035	CACCC		48	GENIC	homozygous	135441964
1	163766036	163766037	C	T	48	GENIC	homozygous	135733899
1	163766657	163766658	T	C	37	GENIC	homozygous	135733900
1	163767110	163767111	C	T	32	GENIC	homozygous	135733901
1	163767770	163767771	A	G	35	GENIC	homozygous	135733902
1	163769297	163769298	T	C	34	GENIC	homozygous	135733903
1	163769405	163769406	G	A	6	GENIC	heterozygous	135733904
1	163772121	163772122	A		42	GENIC	homozygous	135441965
1	163772621	163772622	T	C	60	GENIC	homozygous	135733906
1	163772813	163772822	GACGTCTTA		42	GENIC	homozygous	135441966
1	163773377	163773378	T	C	36	GENIC	homozygous	135733907
1	163774629	163774630	A	T	49	GENIC	possibly homozygous	135733908
1	163760629	163760630	C		33	GENIC	heterozygous	402970983
1	163760629	163760630	C	T	33	GENIC	homozygous	153879246
1	163776749	163776750	A	G	44	GENIC	homozygous	135733909
1	163780331	163780332	G	A	39	GENIC	homozygous	135733914
1	163776819	163776820	T	C	54	GENIC	homozygous	135733910
1	163779208	163779209	C	T	47	GENIC	homozygous	135733911
1	163779718	163779719	A	C	46	GENIC	homozygous	135733912
1	163780024	163780025	A	C	33	GENIC	possibly homozygous	135733913
1	163780880	163780881	C	T	47	GENIC	homozygous	135733915
1	163781410	163781411	A	T	43	GENIC	homozygous	135733916
1	163782659	163782660	T	C	55	GENIC	homozygous	135733917