chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	109505181	109505182	C	A	26	GENIC	homozygous	114859370
13	109505388	109505389	G	C	23	GENIC	homozygous	114443006
13	109505412	109505413	T	C	23	GENIC	homozygous	114859372
13	109506685	109506686	C	T	17	GENIC	homozygous	114443014
13	109509255	109509256	T	C	32	GENIC	homozygous	114859374
13	109509331	109509332	G	A	50	GENIC	homozygous	114443016
13	109509332	109509333	A	T	49	GENIC	homozygous	114443018
13	109509403	109509404	T	G	32	GENIC	homozygous	114443020
13	109509526	109509527	G	C	23	GENIC	homozygous	114443022
13	109509916	109509917	T	C	15	GENIC	homozygous	114700956
13	109516084	109516085	T	C	27	GENIC	homozygous	114443028
13	109516866	109516867	T	C	25	GENIC	homozygous	114859376
13	109517371	109517372	G	A	31	GENIC	homozygous	114859378
13	109517823	109517824	A	G	23	GENIC	homozygous	114443030
13	109520330	109520331	T	C	26	GENIC	homozygous	114443032
13	109520353	109520354	G	A	27	GENIC	homozygous	114443034
13	109512961	109512962	A	C	19	GENIC	heterozygous	114872475