chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50503223	50503224	C	T	24	GENIC	homozygous	126066489
13	50504345	50504346	A	G	14	GENIC	homozygous	126066493
13	50504457	50504458	A	G	13	GENIC	homozygous	126066494
13	50504765	50504766	C	T	17	GENIC	homozygous	126066495
13	50505718	50505719	A	G	9	GENIC	homozygous	126066496
13	50505767	50505768	A	G	26	GENIC	homozygous	126066497
13	50505839	50505840	C	G	17	GENIC	homozygous	126066498
13	50506249	50506250	T	C	4	GENIC	homozygous	126066500
13	50506353	50506354	T	C	12	GENIC	homozygous	126066501
13	50506490	50506491	G	A	12	GENIC	homozygous	126066502
13	50508868	50508869	G	A	10	GENIC	homozygous	126066503
13	50508939	50508940	A	G	8	GENIC	homozygous	126066504
13	50509429	50509430	C	T	14	GENIC	homozygous	126066507
13	50509746	50509747	A	G	9	GENIC	homozygous	126066508
13	50510395	50510396	A	C	17	GENIC	homozygous	126066510
13	50508970	50508971	A	G	9	GENIC	homozygous	126146350