chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	62141111	62141112	A	G	64	GENIC	homozygous	116613384
10	62145534	62145535	G	A	46	GENIC	homozygous	116613390
10	62147828	62147829	A	G	56	GENIC	homozygous	116613394
10	62148443	62148444	T	C	52	GENIC	homozygous	116613396
10	62149953	62149954	A	T	63	GENIC	homozygous	116790933
10	62151565	62151566	T	C	67	GENIC	homozygous	116790935
10	62143551	62143552	T		17	GENIC	possibly homozygous	132692780
10	62144667	62144668	T	A	52	GENIC	homozygous	116939603
10	62147302	62147303	G	A	42	GENIC	homozygous	116939605
10	62150298	62150299	C	T	74	GENIC	homozygous	116939607
10	62154539	62154540	C		28	GENIC	homozygous	128822680
10	62154521	62154522	G		25	GENIC	homozygous	128822679
10	62146051	62146051		GGGTCCCA	49	GENIC	homozygous	128822678
10	62154557	62154558	C		24	GENIC	homozygous	128822681
10	62157818	62157818		T	68	GENIC	homozygous	128822682
10	62158419	62158420	C	T	60	GENIC	homozygous	116613420
10	62163083	62163084	T	C	64	GENIC	homozygous	116613426
10	62164836	62164837	T	A	60	GENIC	homozygous	116790939
10	62176606	62176607	C	A	48	GENIC	homozygous	116790941
10	62179861	62179862	C	T	56	GENIC	homozygous	116790943
10	62180122	62180123	T	C	56	GENIC	homozygous	116613450
10	62185722	62185723	A	G	57	GENIC	homozygous	117997323
10	62186171	62186172	T	C	43	GENIC	homozygous	117104188
10	62163980	62163981	C	A	39	GENIC	possibly homozygous	116978454
10	62186229	62186230	T	C	35	GENIC	homozygous	117997326
10	62189330	62189331	T	A	58	GENIC	homozygous	116613486
10	62170980	62170981	G	A	25	GENIC	homozygous	118041086