chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	60463914	60463917	TGT		16	GENIC	homozygous	132013442
2	60464254	60464254		CT	19	GENIC	homozygous	132013443
2	60464644	60464645	A	T	22	GENIC	homozygous	111108487
2	60465980	60465981	G	A	27	GENIC	homozygous	120168510
2	60466029	60466030	T	G	36	GENIC	homozygous	110538261
2	60466097	60466098	T	C	33	GENIC	homozygous	110538263
2	60466098	60466099	G	A	34	GENIC	homozygous	111108489
2	60466496	60466496		T	9	GENIC	possibly homozygous	132013444
2	60466688	60466688		AAAATT	14	GENIC	homozygous	132013445
2	60466953	60466954	G	C	19	GENIC	homozygous	120168511
2	60468073	60468074	C	A	23	GENIC	homozygous	110538271
2	60468171	60468172	A	G	20	GENIC	homozygous	111108495
2	60468239	60468240	A	T	13	GENIC	homozygous	111108497
2	60468299	60468299		AG	12	GENIC	homozygous	132013446
2	60468604	60468605	C	T	19	GENIC	homozygous	111108501
2	60469048	60469049	C	T	16	GENIC	homozygous	120168512
2	60469293	60469294	T	C	23	GENIC	homozygous	111108503
2	60469481	60469482	G	A	18	GENIC	homozygous	111108505
2	60469593	60469594	G	T	27	GENIC	homozygous	111108507
2	60469629	60469630	A	G	24	GENIC	homozygous	111108509
2	60469633	60469634	T	A	24	GENIC	homozygous	111108511
2	60469634	60469635	C	A	24	GENIC	homozygous	111108513