chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	60461877	60461878	C	T	21	GENIC	homozygous	111108485
2	60464644	60464645	A	T	20	GENIC	homozygous	111108487
2	60463914	60463917	TGT		29	GENIC	homozygous	132013442
2	60464254	60464254		CT	29	GENIC	homozygous	132013443
2	60464595	60464596	A		26	GENIC	homozygous	132804784
2	60466029	60466030	T	G	26	GENIC	homozygous	110538261
2	60466097	60466098	T	C	23	GENIC	homozygous	110538263
2	60466098	60466099	G	A	23	GENIC	homozygous	111108489
2	60466483	60466484	C	T	33	GENIC	homozygous	111108491
2	60466868	60466869	G	A	20	GENIC	homozygous	111108493
2	60468073	60468074	C	A	40	GENIC	homozygous	110538271
2	60468171	60468172	A	G	27	GENIC	homozygous	111108495
2	60468239	60468240	A	T	25	GENIC	homozygous	111108497
2	60468283	60468283		AG	29	GENIC	homozygous	132804785
2	60468604	60468605	C	T	34	GENIC	homozygous	111108501
2	60469293	60469294	T	C	22	GENIC	homozygous	111108503
2	60469481	60469482	G	A	31	GENIC	homozygous	111108505
2	60469633	60469634	T	A	30	GENIC	homozygous	111108511
2	60469593	60469594	G	T	36	GENIC	homozygous	111108507
2	60469629	60469630	A	G	31	GENIC	homozygous	111108509
2	60469634	60469635	C	A	30	GENIC	homozygous	111108513