chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11086792	11086793	T	C	26	GENIC	homozygous	68595900
7	11090399	11090400	A	C	48	GENIC	homozygous	68595902
7	11090441	11090442	C	T	40	GENIC	homozygous	68595904
7	11094804	11094805	C	A	61	GENIC	homozygous	68595907
7	11094903	11094904	G	A	52	GENIC	homozygous	68595909
7	11095092	11095093	G	A	51	GENIC	homozygous	68595912
7	11095588	11095589	G	A	29	GENIC	homozygous	68595914
7	11097965	11097966	G	A	36	GENIC	possibly homozygous	68595917
7	11098016	11098017	G	A	26	GENIC	homozygous	68595920
7	11098017	11098018	G	A	26	GENIC	homozygous	68595923
7	11098287	11098288	A	G	51	GENIC	homozygous	68595925
7	11098563	11098564	A	G	39	GENIC	homozygous	68595928
7	11100226	11100227	C	G	62	GENIC	possibly homozygous	68595929
7	11100286	11100287	G	A	39	GENIC	homozygous	68595932
7	11100674	11100675	C	T	33	GENIC	homozygous	68595935
7	11101153	11101154	C	T	31	GENIC	homozygous	68595937
7	11101166	11101167	G	C	27	GENIC	homozygous	68595940
7	11101263	11101264	C	G	32	GENIC	homozygous	68595943
7	11101315	11101316	C	T	28	GENIC	homozygous	68595946
7	11101445	11101446	C	G	12	GENIC	possibly homozygous	68595949
7	11101483	11101484	C	T	15	GENIC	possibly homozygous	68595950
7	11101538	11101539	C	T	7	GENIC	homozygous	68595955
7	11101547	11101548	A	T	8	GENIC	possibly homozygous	68595958
7	11101567	11101568	A	G	8	GENIC	homozygous	68595960
7	11101826	11101827	C	A	57	GENIC	homozygous	68595965
7	11101834	11101835	G	A	53	GENIC	homozygous	68595968
7	11102143	11102144	A	C	33	GENIC	homozygous	68595970
7	11102177	11102178	C	T	37	GENIC	homozygous	68595973
7	11103374	11103375	T	C	10	GENIC	homozygous	68595976