chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	32608502	32608503	C	A	65	GENIC	homozygous	109168500
20	32608526	32608527	C	T	59	GENIC	homozygous	109168502
20	32609033	32609034	C	G	36	GENIC	homozygous	109168504
20	32609382	32609383	G	A	31	GENIC	homozygous	109168506
20	32610117	32610118	A	G	44	GENIC	homozygous	109168508
20	32610515	32610516	G	A	36	GENIC	homozygous	109168510
20	32610680	32610681	C	T	38	GENIC	homozygous	109168512
20	32610978	32610979	C	G	24	GENIC	possibly homozygous	109168514
20	32611470	32611471	A	G	15	GENIC	homozygous	109168516
20	32611483	32611484	A	G	15	GENIC	possibly homozygous	109168518
20	32612266	32612267	A	G	42	GENIC	homozygous	109168520
20	32613233	32613234	C	T	42	GENIC	homozygous	119786431
20	32613506	32613507	G	A	46	GENIC	homozygous	109168522
20	32613512	32613513	G	T	45	GENIC	homozygous	109168524
20	32613651	32613652	T	C	36	GENIC	homozygous	109168526
20	32613812	32613813	A	C	38	GENIC	homozygous	109168528
20	32615002	32615003	T	C	21	GENIC	possibly homozygous	109168530
20	32615975	32615976	A	C	41	GENIC	homozygous	109168532
20	32620140	32620141	C	T	14	GENIC	homozygous	109578340
20	32620146	32620147	C	T	9	GENIC	possibly homozygous	119786433
20	32620750	32620751	T	C	14	GENIC	homozygous	109168534
20	32620944	32620945	A	G	51	GENIC	homozygous	109168536
20	32621876	32621877	T	C	39	GENIC	possibly homozygous	109168538
20	32622844	32622845	A	T	31	GENIC	homozygous	109168540
20	32623061	32623062	C	A	40	GENIC	homozygous	109168542
20	32623219	32623220	T	C	30	GENIC	homozygous	119786435
20	32625834	32625835	T	C	31	GENIC	possibly homozygous	109168544
20	32626091	32626092	T	G	44	GENIC	possibly homozygous	109493771
20	32628708	32628709	C	T	29	GENIC	homozygous	109168546
20	32628831	32628832	A	G	46	GENIC	homozygous	109168548