chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	60463914	60463917	TGT		47	GENIC	homozygous	132013442
2	60464254	60464254		CT	46	GENIC	homozygous	132013443
2	60464644	60464645	A	T	63	GENIC	homozygous	111108487
2	60465980	60465981	G	A	55	GENIC	homozygous	120168510
2	60466029	60466030	T	G	59	GENIC	homozygous	110538261
2	60466097	60466098	T	C	57	GENIC	homozygous	110538263
2	60466098	60466099	G	A	57	GENIC	homozygous	111108489
2	60466496	60466496		T	38	GENIC	homozygous	132013444
2	60466688	60466688		AAAATT	41	GENIC	homozygous	132013445
2	60466953	60466954	G	C	57	GENIC	homozygous	120168511
2	60468073	60468074	C	A	68	GENIC	homozygous	110538271
2	60468171	60468172	A	G	67	GENIC	homozygous	111108495
2	60468239	60468240	A	T	47	GENIC	homozygous	111108497
2	60468299	60468299		AG	39	GENIC	homozygous	132013446
2	60468604	60468605	C	T	63	GENIC	homozygous	111108501
2	60469048	60469049	C	T	46	GENIC	homozygous	120168512
2	60469293	60469294	T	C	55	GENIC	homozygous	111108503
2	60469481	60469482	G	A	51	GENIC	homozygous	111108505
2	60469593	60469594	G	T	44	GENIC	homozygous	111108507
2	60469629	60469630	A	G	51	GENIC	homozygous	111108509
2	60469633	60469634	T	A	52	GENIC	homozygous	111108511
2	60469634	60469635	C	A	52	GENIC	homozygous	111108513