chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	98252049	98252050	G	A	48	GENIC	homozygous	109942023
2	98252744	98252745	C	T	41	GENIC	possibly homozygous	109942025
2	98254113	98254114	A	G	28	GENIC	possibly homozygous	109942027
2	98254550	98254551	G	C	41	GENIC	homozygous	109942029
2	98256331	98256332	T	C	47	GENIC	homozygous	109942031
2	98257073	98257074	C	T	53	GENIC	homozygous	109942033
2	98257390	98257391	A	T	41	GENIC	homozygous	109942035
2	98257993	98257994	A	G	44	GENIC	homozygous	109942037
2	98258299	98258300	C	T	39	GENIC	homozygous	109942039
2	98258462	98258463	G	T	38	GENIC	homozygous	109942041
2	98258494	98258495	C	G	35	GENIC	homozygous	109942043
2	98259533	98259534	T	A	29	GENIC	homozygous	109942045
2	98259703	98259704	C	A	29	GENIC	homozygous	109942047
2	98259783	98259784	A	G	35	GENIC	homozygous	109942049
2	98259804	98259805	A	G	31	GENIC	homozygous	109942051
2	98259809	98259810	T	G	32	GENIC	homozygous	109942053
2	98259818	98259819	A	G	25	GENIC	homozygous	109942055
2	98259821	98259822	A	G	25	GENIC	homozygous	109942057
2	98259824	98259825	T	G	25	GENIC	homozygous	109942059
2	98254112	98254113	A	G	28	GENIC	possibly homozygous	110723759
2	98260212	98260213	G	A	48	GENIC	homozygous	109942061
2	98260435	98260436	T	C	46	GENIC	homozygous	109942063
2	98261236	98261237	A	G	53	GENIC	homozygous	109942065
2	98261328	98261329	T	G	45	GENIC	homozygous	109942067
2	98261917	98261918	A	G	44	GENIC	homozygous	109942069
2	98262676	98262677	C	G	54	GENIC	homozygous	109942071
2	98263010	98263011	C	T	66	GENIC	homozygous	109942073
2	98263131	98263132	C	G	56	GENIC	homozygous	109942075
2	98263246	98263247	C	G	58	GENIC	homozygous	109942077
2	98264071	98264072	A	G	30	GENIC	homozygous	109942079
2	98265723	98265724	G	A	39	GENIC	possibly homozygous	109942081
2	98266745	98266746	C	T	61	GENIC	homozygous	109942083
2	98267645	98267646	C	T	57	GENIC	heterozygous	109942085
2	98267789	98267790	C	G	50	GENIC	possibly homozygous	109942087