chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	32608265	32608266	T	C	22	GENIC	possibly homozygous	109398500
20	32608502	32608503	C	A	22	GENIC	homozygous	109168500
20	32608526	32608527	C	T	30	GENIC	homozygous	109168502
20	32609033	32609034	C	G	27	GENIC	homozygous	109168504
20	32610117	32610118	A	G	17	GENIC	homozygous	109168508
20	32610713	32610714	T	C	15	GENIC	homozygous	109253458
20	32610866	32610867	A	G	24	GENIC	homozygous	109398501
20	32610978	32610979	C	G	17	GENIC	possibly homozygous	109168514
20	32611483	32611484	A	G	14	GENIC	homozygous	109168518
20	32611519	32611520	C	A	21	GENIC	homozygous	109398502
20	32611634	32611635	G	C	22	GENIC	homozygous	109398503
20	32611642	32611643	C	T	20	GENIC	homozygous	109253468
20	32611083	32611084	C	T	3	GENIC	homozygous	109578336
20	32611239	32611240	G	A	20	GENIC	homozygous	109578338
20	32615975	32615976	A	C	15	GENIC	homozygous	109168532
20	32620140	32620141	C	T	2	GENIC	homozygous	109578340
20	32620144	32620145	C	T	2	GENIC	homozygous	109578342
20	32623061	32623062	C	A	21	GENIC	possibly homozygous	109168542
20	32628308	32628309	C	T	18	GENIC	possibly homozygous	109398504
20	32628708	32628709	C	T	17	GENIC	possibly homozygous	109168546
20	32628831	32628832	A	G	23	GENIC	possibly homozygous	109168548