chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30372673	30372674	A	G	8	GENIC	heterozygous	126269973
11	30374294	30374295	G	A	19	GENIC	homozygous	126269975
11	30375328	30375329	A	G	11	GENIC	homozygous	126269977
11	30384582	30384583	T	G	14	GENIC	homozygous	126269979
11	30384928	30384929	C	T	27	GENIC	homozygous	126269981
11	30385733	30385734	A	T	29	GENIC	homozygous	126269983
11	30386001	30386002	T	C	18	GENIC	homozygous	126269985
11	30387122	30387123	G	A	26	GENIC	homozygous	126269987
11	30390433	30390434	T	A	10	GENIC	homozygous	126269989
11	30390990	30390991	C	A	20	GENIC	homozygous	126269991
11	30392489	30392490	G	T	10	GENIC	heterozygous	126269993
11	30393574	30393575	C	G	26	GENIC	homozygous	126269995
11	30394863	30394864	C	T	16	GENIC	homozygous	126269997
11	30397272	30397273	G	A	9	GENIC	homozygous	126269999
11	30402844	30402845	G	A	21	GENIC	homozygous	126270001
11	30412709	30412710	T	C	22	GENIC	homozygous	126270003
11	30413067	30413068	T	C	8	GENIC	homozygous	126270005
11	30413203	30413204	T	G	16	GENIC	homozygous	126270007
11	30414785	30414786	G	A	6	GENIC	homozygous	126270009
11	30414787	30414788	C	T	7	GENIC	homozygous	115808411
11	30415285	30415286	A	C	21	GENIC	homozygous	126270011
11	30415498	30415499	T	C	14	GENIC	homozygous	126270013
11	30415511	30415512	C	T	17	GENIC	homozygous	126270015
11	30415574	30415575	A	T	22	GENIC	homozygous	126270017
11	30423461	30423462	T	C	9	GENIC	homozygous	126270019
11	30423955	30423956	C	A	21	GENIC	homozygous	126270021
11	30425677	30425678	G	A	8	GENIC	heterozygous	126270023
11	30426332	30426333	A	G	10	GENIC	heterozygous	126270025