chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	36095798	36095799	A	G	22	GENIC	homozygous	115024271
13	36095820	36095821	C	A	23	GENIC	homozygous	115024272
13	36095847	36095848	A	G	17	GENIC	homozygous	115024273
13	36095886	36095887	T	C	19	GENIC	homozygous	115024274
13	36096451	36096452	T	G	25	GENIC	homozygous	115024275
13	36096568	36096569	T	C	31	GENIC	homozygous	115024276
13	36097195	36097196	T	C	37	GENIC	possibly homozygous	115024277
13	36098210	36098211	T	A	14	GENIC	homozygous	115024278
13	36098286	36098287	T	C	17	GENIC	homozygous	114313909
13	36099056	36099057	T	C	28	GENIC	homozygous	114313910
13	36099635	36099636	C	T	16	GENIC	homozygous	114313912
13	36099661	36099662	G	C	17	GENIC	homozygous	114313913
13	36099662	36099663	G	C	17	GENIC	homozygous	114313914
13	36099664	36099665	G	C	18	GENIC	homozygous	114313915
13	36099794	36099795	C	T	16	GENIC	homozygous	114313916
13	36099910	36099911	A	G	12	GENIC	homozygous	114313917
13	36100114	36100115	G	A	18	GENIC	homozygous	114313918
13	36100382	36100383	A	G	20	GENIC	homozygous	114313919
13	36100389	36100390	T	C	19	GENIC	homozygous	114313920
13	36100684	36100685	G	T	33	GENIC	homozygous	115024279
13	36100847	36100848	T	G	29	GENIC	homozygous	114313921
13	36100969	36100970	C	A	26	GENIC	homozygous	114820058
13	36100971	36100972	G	T	25	GENIC	homozygous	114820060
13	36101163	36101164	C	G	17	GENIC	homozygous	114313922