chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	45104884	45104885	C	G	39	GENIC	homozygous	109726350
2	45104943	45104944	G	T	36	GENIC	homozygous	109726352
2	45104988	45104989	C	A	46	GENIC	homozygous	109726354
2	45108293	45108294	G	A	35	GENIC	homozygous	110693033
2	45109507	45109508	T	C	21	GENIC	possibly homozygous	110693035
2	45109785	45109786	A	G	28	GENIC	homozygous	109726366
2	45109862	45109863	A	G	29	GENIC	homozygous	110693037
2	45110025	45110026	G	A	21	GENIC	homozygous	110693039
2	45110980	45110981	T	C	35	GENIC	homozygous	109726370
2	45110985	45110986	A	G	37	GENIC	homozygous	109726372
2	45110991	45110992	T	C	37	GENIC	homozygous	109726374
2	45111215	45111216	G	T	31	GENIC	homozygous	109726376
2	45111239	45111240	G	C	30	GENIC	homozygous	109726378
2	45111483	45111484	T	C	29	GENIC	homozygous	110508587
2	45112226	45112227	A	G	20	GENIC	homozygous	109726380
2	45112952	45112953	C	G	20	GENIC	homozygous	109726384