chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	36090974	36090975	T	A	43	GENIC	homozygous	115103795
6	36092605	36092606	T		30	GENIC	homozygous	132092198
6	36095014	36095015	A	G	55	GENIC	homozygous	115103796
6	36095157	36095158	C	G	42	GENIC	possibly homozygous	115103797
6	36095475	36095475		A	51	GENIC	possibly homozygous	132092199
6	36097039	36097040	G	A	39	GENIC	homozygous	115103798
6	36097945	36097946	G	T	42	GENIC	homozygous	115103799
6	36101032	36101032		G	11	GENIC	homozygous	128329511
6	36095240	36095241	G		41	GENIC	homozygous	130325964
6	36100945	36100945		A	15	GENIC	homozygous	128329508
6	36100985	36100985		GG	17	GENIC	homozygous	128329509
6	36100989	36100990	A		17	GENIC	homozygous	128329510
6	36101083	36101084	C		24	GENIC	homozygous	132092201
6	36101121	36101121		T	21	GENIC	homozygous	128329512
6	36101135	36101135		T	19	GENIC	homozygous	128329513
6	36101178	36101178		T	15	GENIC	homozygous	128329514
6	36102519	36102520	C	T	46	GENIC	homozygous	115103800
6	36102825	36102826	C	A	40	GENIC	homozygous	115103801
6	36102826	36102827	G	A	41	GENIC	homozygous	115103802
6	36102882	36102883	C	T	45	GENIC	homozygous	115103803
6	36103961	36103962	C	T	29	GENIC	homozygous	115103806
6	36101633	36101634	T		45	GENIC	possibly homozygous	131407316
6	36102890	36102891	G	A	52	GENIC	homozygous	115103804
6	36103640	36103641	A	G	40	GENIC	homozygous	115103805
6	36104004	36104005	T	C	39	GENIC	homozygous	115103807
6	36104005	36104006	G	A	38	GENIC	homozygous	115103808
6	36105336	36105337	A	T	45	GENIC	homozygous	115103809