chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	98252938	98252939	C	T	10	GENIC	homozygous	110576374
2	98254532	98254533	C	T	8	GENIC	homozygous	110576376
2	98256316	98256317	T	G	7	GENIC	homozygous	110576380
2	98256331	98256332	T	C	4	GENIC	homozygous	109942031
2	98258299	98258300	C	T	7	GENIC	homozygous	109942039
2	98259703	98259704	C	A	5	GENIC	homozygous	109942047
2	98259783	98259784	A	G	4	GENIC	homozygous	109942049
2	98260212	98260213	G	A	25	GENIC	homozygous	109942061
2	98260435	98260436	T	C	20	GENIC	homozygous	109942063
2	98261236	98261237	A	G	5	GENIC	homozygous	109942065
2	98261328	98261329	T	G	16	GENIC	homozygous	109942067
2	98261917	98261918	A	G	12	GENIC	homozygous	109942069
2	98263010	98263011	C	T	27	GENIC	homozygous	109942073
2	98263131	98263132	C	G	21	GENIC	homozygous	109942075
2	98263246	98263247	C	G	19	GENIC	homozygous	109942077
2	98265723	98265724	G	A	18	GENIC	homozygous	109942081
2	98266222	98266223	A	T	4	GENIC	homozygous	110576386
2	98266554	98266555	C	G	22	GENIC	homozygous	110576388
2	98266859	98266860	G	A	18	GENIC	homozygous	110576390
2	98267645	98267646	C	T	6	GENIC	homozygous	109942085
2	98268462	98268463	C	T	16	GENIC	homozygous	110576392