chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	48489135	48489136	T	G	34	GENIC	homozygous	109737362
2	48489346	48489347	C	T	45	GENIC	homozygous	109737364
2	48489924	48489925	T	C	51	GENIC	homozygous	109737366
2	48490164	48490165	T	C	19	GENIC	homozygous	109737368
2	48490665	48490666	G	C	25	GENIC	homozygous	109737370
2	48490857	48490858	A	C	11	GENIC	homozygous	109737372
2	48490860	48490861	A	C	13	GENIC	homozygous	109737374
2	48491396	48491397	G	A	35	GENIC	homozygous	109737376
2	48492202	48492203	A	G	46	GENIC	possibly homozygous	109737378
2	48492639	48492640	T	C	25	GENIC	homozygous	109737380
2	48492898	48492899	G	T	41	GENIC	homozygous	109737382
2	48495138	48495139	C	T	57	GENIC	homozygous	109737384
2	48495652	48495653	A	C	43	GENIC	homozygous	109737386
2	48495856	48495857	G	A	36	GENIC	possibly homozygous	109737388
2	48496613	48496614	G	A	16	GENIC	homozygous	109737390
2	48496728	48496729	G	A	23	GENIC	homozygous	109737392
2	48496732	48496733	C	A	23	GENIC	homozygous	109737394
2	48497318	48497319	T	C	16	GENIC	homozygous	109737396
2	48499746	48499747	T	C	40	GENIC	homozygous	109737400
2	48499713	48499714	A	C	34	GENIC	homozygous	109737398