chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	61552071	61552072	G	A	64	GENIC	homozygous	133504790
15	61552136	61552137	T	G	69	GENIC	homozygous	119024638
15	61552155	61552156	G	A	68	GENIC	homozygous	133504791
15	61552310	61552311	G	A	55	GENIC	homozygous	113006697
15	61552433	61552434	A	G	51	GENIC	homozygous	113006699
15	61553062	61553063	C	T	48	GENIC	homozygous	113006701
15	61553099	61553100	G	A	53	GENIC	homozygous	113006703
15	61553673	61553674	C	T	46	GENIC	homozygous	113006705
15	61553882	61553883	G	C	60	GENIC	homozygous	113006707
15	61553947	61553948	C	T	61	GENIC	homozygous	113006709
15	61553956	61553957	A	G	61	GENIC	homozygous	113006711
15	61554186	61554187	A	G	48	GENIC	homozygous	113006713
15	61554247	61554248	T	G	45	GENIC	homozygous	113006715
15	61554583	61554584	A	C	51	GENIC	homozygous	113006717
15	61555037	61555038	A	G	51	GENIC	homozygous	113006719
15	61555352	61555353	T	C	59	GENIC	homozygous	113006721
15	61556206	61556207	C	T	41	GENIC	homozygous	113006723
15	61557194	61557195	A	G	55	GENIC	homozygous	113006725
15	61553577	61553577		G	54	GENIC	homozygous	129262159
15	61552676	61552676		A	20	GENIC	homozygous	133502059
15	61553873	61553874	C		54	GENIC	homozygous	133502060
15	61556043	61556053	AAACAAAACT		52	GENIC	homozygous	133502061
15	61557491	61557492	A	G	59	GENIC	possibly homozygous	113006727
15	61558638	61558639	G	A	47	GENIC	homozygous	112698620
15	61559234	61559236	GG		19	GENIC	homozygous	133776249
15	61559257	61559258	G		25	GENIC	homozygous	133776250
15	61559966	61559967	G		63	GENIC	homozygous	129262160
15	61560396	61560397	A	G	57	GENIC	homozygous	113006731
15	61560921	61560924	AAT		46	GENIC	homozygous	133502062
15	61561032	61561033	T	C	46	GENIC	homozygous	113006733
15	61561400	61561400		TGT	47	GENIC	possibly homozygous	133502063
15	61560876	61560879	AAT		42	GENIC	heterozygous	135013355
15	61561803	61561804	A	G	55	GENIC	homozygous	113006735