chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	90733464	90733465	G	GT	22	GENIC	homozygous	52037420
9	90733496	90733497	G	GT	25	GENIC	homozygous	52037422
9	90733844	90733846	GT	--	5	GENIC	heterozygous	52914976
9	90735882	90735884	GT	--	18	GENIC	heterozygous	52914977
9	90736030	90736031	T	TGGGA	30	GENIC	homozygous	52037438
9	90736878	90736879	T	G	26	GENIC	homozygous	52037448
9	90736921	90736922	T	G	27	GENIC	homozygous	52037450
9	90736932	90736933	T	G	27	GENIC	homozygous	52037452
9	90736946	90736947	A	G	26	GENIC	homozygous	52037454
9	90736954	90736955	T	G	26	GENIC	homozygous	52037456
9	90736971	90736972	T	A	25	GENIC	homozygous	52037458
9	90738562	90738563	T	C	16	GENIC	homozygous	52037466
9	90740610	90740612	AT	--	1	GENIC	homozygous	52037484
9	90741455	90741456	A	AAGG	17	GENIC	homozygous	52037494
9	90742426	90742428	AA	--	5	GENIC	homozygous	52037516
9	90742583	90742584	C	T	10	GENIC	homozygous	52037524
9	90742585	90742586	T	C	11	GENIC	homozygous	52037526
9	90742599	90742600	C	A	22	GENIC	homozygous	52037527
9	90742601	90742602	G	T	22	GENIC	homozygous	52037529
9	90742604	90742606	CC	--	22	GENIC	homozygous	52037531
9	90742611	90742612	C	A	23	GENIC	homozygous	52037533
9	90742808	90742809	A	AG	6	GENIC	homozygous	52914978
9	90747690	90747691	T	TAG	18	GENIC	homozygous	52037555
9	90747950	90747951	C	T	31	GENIC	homozygous	52037565
9	90748694	90748696	GT	--	7	GENIC	heterozygous	52914979
9	90742610	90742611	C	T	23	GENIC	homozygous	52861259
9	90736032	90736033	T	G	30	GENIC	homozygous	52861255