chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30728600	30728601	G	A	26	GENIC	homozygous	138952910
11	30730812	30730813	G	A	27	GENIC	homozygous	138952911
11	30731393	30731394	T	G	24	GENIC	homozygous	138952912
11	30731608	30731609	T	C	24	GENIC	homozygous	138952913
11	30732021	30732022	C	T	31	GENIC	homozygous	138952914
11	30732319	30732320	T	C	20	GENIC	homozygous	138952915
11	30732894	30732897	TTG		21	GENIC	homozygous	138880785
11	30736064	30736064		A	9	GENIC	homozygous	138880786
11	30736930	30736931	T	A	38	GENIC	homozygous	138952916
11	30737090	30737090		C	33	GENIC	possibly homozygous	138880787
11	30737859	30737860	G	A	19	GENIC	homozygous	138952917
11	30738844	30738845	T	A	31	GENIC	homozygous	138952918
11	30739071	30739072	G	A	28	GENIC	homozygous	138952919
11	30739954	30739955	A	T	35	GENIC	homozygous	138952920
11	30740561	30740562	G	A	26	GENIC	homozygous	138952921
11	30740748	30740749	A	T	23	GENIC	homozygous	138952922
11	30740904	30740905	G	A	31	GENIC	homozygous	138952923
11	30740998	30740999	T	G	34	GENIC	homozygous	138952924
11	30742025	30742026	A	C	25	GENIC	homozygous	138952925
11	30742626	30742627	G	A	26	GENIC	homozygous	138952926
11	30743472	30743473	G	C	9	GENIC	homozygous	138952931
11	30743535	30743536	G		15	GENIC	homozygous	138880788
11	30743826	30743827	A	G	19	GENIC	homozygous	138952932
11	30745384	30745385	T	C	19	GENIC	homozygous	138952933
11	30750007	30750008	G	C	23	GENIC	homozygous	138952934
11	30751715	30751716	C	T	29	GENIC	homozygous	138952935
11	30734578	30734579	C	T	2	GENIC	homozygous	147696097
11	30734581	30734582	C	A	1	GENIC	homozygous	147696098
11	30734583	30734584	C	G	1	GENIC	homozygous	147696099