chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	54953291	54953292	G	T	20	GENIC	homozygous	58827950
2	54954091	54954092	T	A	8	GENIC	homozygous	58827952
2	54954097	54954098	C	G	10	GENIC	possibly homozygous	58827953
2	54956805	54956806	G	-	12	GENIC	homozygous	58827960
2	54956893	54956894	T	C	16	GENIC	possibly homozygous	58827961
2	54957410	54957411	C	T	24	GENIC	homozygous	58827962
2	54957449	54957450	C	T	19	GENIC	homozygous	58827963
2	54957520	54957521	G	A	24	GENIC	homozygous	58827964
2	54958484	54958485	T	C	17	GENIC	homozygous	58827965
2	54958685	54958686	C	T	11	GENIC	possibly homozygous	58827966
2	54959040	54959041	G	A	16	GENIC	possibly homozygous	58827967
2	54959451	54959452	T	C	7	GENIC	homozygous	58827968
2	54960486	54960487	G	A	21	GENIC	possibly homozygous	58827969
2	54960717	54960718	T	C	25	GENIC	homozygous	58827970
2	54961131	54961132	A	G	9	GENIC	homozygous	58827971
2	54961141	54961142	C	A	7	GENIC	homozygous	58827972
2	54961158	54961159	C	T	9	GENIC	homozygous	58827973
2	54961282	54961283	T	G	12	GENIC	homozygous	58827974
2	54961293	54961294	A	G	9	GENIC	possibly homozygous	58827975
2	54961615	54961616	G	GAGAAA	2	GENIC	homozygous	58827979
2	54963289	54963290	A	C	10	GENIC	homozygous	58827980
2	54964092	54964093	A	G	13	GENIC	homozygous	58827982
2	54965449	54965450	C	T	11	GENIC	possibly homozygous	58827988
2	54966029	54966030	A	G	13	GENIC	homozygous	58827989
2	54966071	54966072	G	A	7	GENIC	heterozygous	58827990
2	54966424	54966425	T	C	23	GENIC	homozygous	58827998