chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	45104884	45104885	C	G	55	GENIC	homozygous	109726350
2	45104943	45104944	G	T	63	GENIC	possibly homozygous	109726352
2	45104988	45104989	C	A	57	GENIC	homozygous	109726354
2	45105885	45105886	C	G	65	GENIC	possibly homozygous	110508586
2	45109785	45109786	A	G	64	GENIC	homozygous	109726366
2	45110980	45110981	T	C	49	GENIC	homozygous	109726370
2	45110985	45110986	A	G	47	GENIC	homozygous	109726372
2	45110991	45110992	T	C	44	GENIC	homozygous	109726374
2	45111239	45111240	G	C	97	GENIC	possibly homozygous	109726378
2	45111483	45111484	T	C	52	GENIC	homozygous	110508587
2	45111940	45111941	T	C	38	GENIC	homozygous	110508588
2	45112129	45112130	T	A	55	GENIC	possibly homozygous	110508589
2	45112226	45112227	A	G	69	GENIC	homozygous	109726380
2	45112386	45112387	T	A	64	GENIC	possibly homozygous	110508590
2	45112621	45112622	C	T	66	GENIC	homozygous	109726382
2	45112952	45112953	C	G	62	GENIC	homozygous	109726384
2	45113078	45113079	A	G	44	GENIC	homozygous	109726386
2	45113093	45113094	T	A	56	GENIC	possibly homozygous	109726388