chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230655712	230655713	C	G	18	GENIC	homozygous	59432456
2	230656955	230656957	TT	--	1	GENIC	homozygous	60520714
2	230658581	230658582	T	A	30	GENIC	homozygous	59432458
2	230659376	230659377	C	T	20	GENIC	possibly homozygous	59432459
2	230660489	230660490	T	C	19	GENIC	homozygous	59432460
2	230661219	230661220	G	GGA	5	GENIC	heterozygous	59432463
2	230661739	230661740	G	A	35	GENIC	homozygous	59432466
2	230662330	230662331	G	GC	16	GENIC	possibly homozygous	59432467
2	230665992	230665993	T	TCC	8	GENIC	possibly homozygous	59432468
2	230665992	230665993	T	TC	8	GENIC	heterozygous	60168652
2	230666172	230666173	A	G	17	GENIC	possibly homozygous	59432469
2	230666570	230666571	C	T	17	GENIC	heterozygous	59432470
2	230666987	230666988	T	C	23	GENIC	possibly homozygous	59432471
2	230667264	230667265	C	T	29	GENIC	homozygous	59432472
2	230667720	230667721	A	T	21	GENIC	homozygous	59432473
2	230667944	230667946	CT	--	3	GENIC	homozygous	59432474
2	230667951	230667952	G	-	3	GENIC	homozygous	59432475
2	230668118	230668119	G	A	11	GENIC	possibly homozygous	59432476
2	230670041	230670042	T	C	21	GENIC	homozygous	59432477
2	230670716	230670717	G	A	29	GENIC	homozygous	59432478
2	230672185	230672186	C	CAAAGACCCAGGA	5	GENIC	homozygous	59432480
2	230673694	230673695	T	C	5	GENIC	homozygous	59432482
2	230673759	230673760	T	-	3	GENIC	homozygous	60085450
2	230675478	230675479	A	G	16	GENIC	homozygous	59432483
2	230676081	230676082	A	G	23	GENIC	possibly homozygous	59432484