chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	41608595	41608596	G	T	80	GENIC	possibly homozygous	108090613
1	41608617	41608618	C	T	76	GENIC	possibly homozygous	108090614
1	41608760	41608761	G	A	54	GENIC	possibly homozygous	108090615
1	41608762	41608763	G	C	53	GENIC	possibly homozygous	108090616
1	41608768	41608769	A	G	59	GENIC	possibly homozygous	108090617
1	41644284	41644285	G	A	26	GENIC	homozygous	108090618
1	41644286	41644287	G	C	26	GENIC	homozygous	108090619
1	41644288	41644289	G	C	26	GENIC	homozygous	108090620
1	41644289	41644290	G	C	26	GENIC	homozygous	108090621
1	41644290	41644291	G	A	27	GENIC	homozygous	108090622
1	41675038	41675039	G	A	48	GENIC	homozygous	108090623
1	41675321	41675322	G	C	26	GENIC	homozygous	108090625
1	41675350	41675351	C	A	33	GENIC	homozygous	108090626
1	41684921	41684922	T	A	46	GENIC	homozygous	108090627
1	41687748	41687749	C	T	36	GENIC	homozygous	108090628
1	41687845	41687846	C	T	20	GENIC	homozygous	108090629
1	41736594	41736595	A	G	4	GENIC	homozygous	108090630
1	41742364	41742365	G	A	19	GENIC	homozygous	108090631
1	41742375	41742376	T	A	21	GENIC	homozygous	108090632
1	41742387	41742388	T	A	32	GENIC	homozygous	108090633
1	41742390	41742391	T	A	32	GENIC	homozygous	108090634
1	41747091	41747092	G	T	54	GENIC	homozygous	108090635