chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47300732	47300733	T	C	46	GENIC	homozygous	51637879
10	47300827	47300828	C	T	49	GENIC	homozygous	51637880
10	47301519	47301520	C	T	60	GENIC	homozygous	51637881
10	47304147	47304148	A	G	54	GENIC	homozygous	51637882
10	47305094	47305095	C	T	61	GENIC	homozygous	51637883
10	47305783	47305784	T	-	26	GENIC	homozygous	51637884
10	47307995	47307996	A	G	70	GENIC	possibly homozygous	51637885
10	47308413	47308414	G	C	44	GENIC	homozygous	51637886
10	47308428	47308429	C	A	46	GENIC	homozygous	51637887
10	47308907	47308908	A	AATG	44	GENIC	homozygous	51637888
10	47309864	47309865	G	GAGAGGGAC	18	GENIC	homozygous	51637889
10	47309889	47309890	T	G	28	GENIC	homozygous	51637890
10	47309985	47309986	G	A	49	GENIC	homozygous	51637891
10	47310374	47310375	A	G	65	GENIC	homozygous	51637892
10	47310421	47310422	C	A	52	GENIC	homozygous	51637893
10	47310734	47310735	T	C	48	GENIC	homozygous	51637894
10	47310897	47310898	A	AAAG	51	GENIC	homozygous	51637895
10	47311238	47311239	C	T	60	GENIC	homozygous	51637896
10	47311757	47311758	A	-	37	GENIC	heterozygous	51637897
10	47311758	47311759	A	G	58	GENIC	homozygous	51637898
10	47311762	47311763	A	G	59	GENIC	homozygous	51637899
10	47311791	47311792	G	A	44	GENIC	homozygous	51637900
10	47312065	47312066	C	T	44	GENIC	homozygous	51637901
10	47312753	47312754	C	T	68	GENIC	homozygous	51637902
10	47313341	47313345	TTTT	----	39	GENIC	homozygous	51637903
10	47313627	47313628	T	TCCAACC	26	GENIC	homozygous	51637904
10	47313826	47313827	T	C	37	GENIC	homozygous	51637905
10	47314511	47314512	G	A	47	GENIC	homozygous	51637906
10	47314728	47314729	C	A	55	GENIC	possibly homozygous	51637907
10	47316814	47316815	C	T	45	GENIC	homozygous	51637908
10	47317359	47317360	A	C	46	GENIC	homozygous	51637909
10	47318953	47318954	C	T	66	GENIC	homozygous	51637910
10	47319184	47319188	ATAT	----	40	GENIC	homozygous	51637911
10	47319491	47319492	A	-	34	GENIC	homozygous	51637912
10	47317501	47317502	A	-	1	GENIC	homozygous	51445683