chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	48489135	48489136	T	G	43	GENIC	homozygous	109737362
2	48489346	48489347	C	T	43	GENIC	homozygous	109737364
2	48489924	48489925	T	C	48	GENIC	homozygous	109737366
2	48490164	48490165	T	C	44	GENIC	homozygous	109737368
2	48490665	48490666	G	C	30	GENIC	homozygous	109737370
2	48490857	48490858	A	C	15	GENIC	homozygous	109737372
2	48490860	48490861	A	C	17	GENIC	homozygous	109737374
2	48491396	48491397	G	A	45	GENIC	homozygous	109737376
2	48492202	48492203	A	G	47	GENIC	homozygous	109737378
2	48492639	48492640	T	C	47	GENIC	homozygous	109737380
2	48492898	48492899	G	T	50	GENIC	homozygous	109737382
2	48495138	48495139	C	T	36	GENIC	possibly homozygous	109737384
2	48495652	48495653	A	C	52	GENIC	homozygous	109737386
2	48495856	48495857	G	A	20	GENIC	homozygous	109737388
2	48496613	48496614	G	A	35	GENIC	homozygous	109737390
2	48496728	48496729	G	A	33	GENIC	homozygous	109737392
2	48496732	48496733	C	A	35	GENIC	homozygous	109737394
2	48497318	48497319	T	C	61	GENIC	homozygous	109737396
2	48495535	48495535		AAAAC	27	GENIC	homozygous	127619793
2	48496455	48496455		T	23	GENIC	homozygous	127619794
2	48497867	48497869	TT		35	GENIC	homozygous	127619795
2	48499706	48499707	G		21	GENIC	homozygous	127619796
2	48499713	48499714	A	C	22	GENIC	homozygous	109737398
2	48499722	48499723	C		22	GENIC	homozygous	127619797
2	48499746	48499747	T	C	25	GENIC	homozygous	109737400
2	48499783	48499784	C		25	GENIC	homozygous	127619798