chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30728600	30728601	G	A	48	GENIC	homozygous	138952910
11	30730812	30730813	G	A	60	GENIC	homozygous	138952911
11	30731393	30731394	T	G	62	GENIC	possibly homozygous	138952912
11	30731608	30731609	T	C	53	GENIC	homozygous	138952913
11	30732021	30732022	C	T	62	GENIC	possibly homozygous	138952914
11	30732319	30732320	T	C	63	GENIC	homozygous	138952915
11	30732894	30732897	TTG		62	GENIC	homozygous	138880785
11	30736064	30736064		A	67	GENIC	possibly homozygous	138880786
11	30736930	30736931	T	A	64	GENIC	homozygous	138952916
11	30737090	30737090		C	45	GENIC	possibly homozygous	138880787
11	30737859	30737860	G	A	70	GENIC	homozygous	138952917
11	30738844	30738845	T	A	65	GENIC	possibly homozygous	138952918
11	30739071	30739072	G	A	81	GENIC	homozygous	138952919
11	30739954	30739955	A	T	75	GENIC	possibly homozygous	138952920
11	30740561	30740562	G	A	65	GENIC	homozygous	138952921
11	30740748	30740749	A	T	67	GENIC	homozygous	138952922
11	30740904	30740905	G	A	59	GENIC	homozygous	138952923
11	30740998	30740999	T	G	75	GENIC	homozygous	138952924
11	30742025	30742026	A	C	73	GENIC	homozygous	138952925
11	30742626	30742627	G	A	65	GENIC	homozygous	138952926
11	30743439	30743440	G	A	24	GENIC	homozygous	138952927
11	30743451	30743452	C	T	31	GENIC	homozygous	138952928
11	30743535	30743536	G		48	GENIC	homozygous	138880788
11	30743826	30743827	A	G	48	GENIC	homozygous	138952932
11	30743454	30743455	G	A	32	GENIC	homozygous	138952929
11	30743468	30743469	G	A	37	GENIC	homozygous	138952930
11	30743472	30743473	G	C	37	GENIC	homozygous	138952931
11	30745384	30745385	T	C	80	GENIC	homozygous	138952933
11	30750007	30750008	G	C	77	GENIC	homozygous	138952934
11	30751715	30751716	C	T	77	GENIC	homozygous	138952935