chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11817811	11817812	C	CTG	21	GENIC	homozygous	47020976
17	11817989	11817990	A	AACAT	10	GENIC	homozygous	47020977
17	11817997	11817998	G	A	10	GENIC	heterozygous	47020978
17	11818010	11818011	T	G	9	GENIC	heterozygous	47020982
17	11819710	11819711	C	T	26	GENIC	homozygous	47020983
17	11820396	11820397	C	T	32	GENIC	homozygous	47020984
17	11820981	11820982	T	TAC	18	GENIC	heterozygous	47020985
17	11821015	11821017	CG	--	32	GENIC	heterozygous	47020986
17	11821813	11821814	A	G	26	GENIC	homozygous	47020987
17	11821905	11821906	T	C	16	GENIC	homozygous	47020988
17	11822041	11822042	C	CT	3	GENIC	heterozygous	47020989
17	11822041	11822042	C	CTTT	3	GENIC	heterozygous	47020990
17	11822129	11822132	TTT	---	3	GENIC	heterozygous	47020991
17	11822130	11822132	TT	--	3	GENIC	heterozygous	47020992
17	11822498	11822499	C	T	23	GENIC	homozygous	47020993
17	11822650	11822651	G	A	22	GENIC	homozygous	47020994
17	11825944	11825947	AGG	---	23	GENIC	homozygous	47020995
17	11828942	11828943	A	G	18	GENIC	homozygous	47020996
17	11829352	11829353	G	A	37	GENIC	homozygous	47020997
17	11830600	11830605	CGGCT	-----	4	GENIC	homozygous	47529766