chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	17228989	17228990	A	G	32	GENIC	homozygous	113361717
14	17229302	17229303	A	T	21	GENIC	homozygous	113361721
14	17230747	17230748	T	C	22	GENIC	homozygous	113361723
14	17231158	17231159	T	A	40	GENIC	homozygous	113361725
14	17231460	17231461	T	C	16	GENIC	homozygous	113361727
14	17232561	17232562	C	T	29	GENIC	possibly homozygous	113809563
14	17232821	17232822	T	C	26	GENIC	homozygous	113361737
14	17233276	17233277	A	G	32	GENIC	homozygous	113809565
14	17233284	17233285	A	G	30	GENIC	possibly homozygous	113809567
14	17233286	17233287	T	G	32	GENIC	possibly homozygous	114042189
14	17233334	17233335	A	T	37	GENIC	possibly homozygous	113809569
14	17233384	17233385	A	G	37	GENIC	possibly homozygous	113809571
14	17233428	17233429	C	A	32	GENIC	possibly homozygous	113809573
14	17233494	17233495	A	G	35	GENIC	possibly homozygous	113809575
14	17233603	17233604	G	A	25	GENIC	possibly homozygous	113809577
14	17233715	17233716	A	G	26	GENIC	possibly homozygous	113809579