chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	45104988	45104989	C	A	69	GENIC	homozygous	109726354
2	45108505	45108506	G	T	52	GENIC	homozygous	109726358
2	45108791	45108792	T	C	55	GENIC	homozygous	109726360
2	45109652	45109653	A	T	50	GENIC	homozygous	109726364
2	45109785	45109786	A	G	54	GENIC	homozygous	109726366
2	45110963	45110965	GT		51	GENIC	homozygous	127617819
2	45110980	45110981	T	C	49	GENIC	homozygous	109726370
2	45110985	45110986	A	G	48	GENIC	homozygous	109726372
2	45110991	45110992	T	C	48	GENIC	homozygous	109726374
2	45111215	45111216	G	T	44	GENIC	possibly homozygous	109726376
2	45111239	45111240	G	C	50	GENIC	homozygous	109726378
2	45111483	45111484	T	C	47	GENIC	homozygous	110508587
2	45112226	45112227	A	G	50	GENIC	homozygous	109726380
2	45112952	45112953	C	G	46	GENIC	homozygous	109726384
2	45109505	45109506	T	A	54	GENIC	homozygous	120167459
2	45112383	45112383		AT	45	GENIC	homozygous	130862182