chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	100279101	100279102	G	C	20	GENIC	homozygous	52076743
9	100280091	100280092	A	G	18	GENIC	homozygous	52076745
9	100280950	100280951	C	CTTT	12	GENIC	heterozygous	52076747
9	100280951	100280952	T	-	12	GENIC	possibly homozygous	52076749
9	100281459	100281461	TT	--	1	GENIC	homozygous	52076751
9	100281889	100281890	T	TTAA	22	GENIC	homozygous	52076753
9	100282301	100282302	G	GA	17	GENIC	homozygous	52076755
9	100282694	100282695	A	G	31	GENIC	homozygous	52076757
9	100283028	100283029	A	AGT	23	GENIC	heterozygous	52076759
9	100284478	100284479	C	CATGAGACACT	18	GENIC	homozygous	52076761
9	100291661	100291662	A	C	39	GENIC	homozygous	52076763
9	100291755	100291756	C	A	20	GENIC	homozygous	52076765
9	100291972	100291973	A	T	36	GENIC	homozygous	52076767
9	100294232	100294233	C	-	35	GENIC	homozygous	52076769
9	100297159	100297162	ACT	---	6	GENIC	homozygous	52076771
9	100297165	100297197	AAATGTTAAATATGTTAAATGTTAAATGTTAA	--------------------------------	6	GENIC	homozygous	52076773
9	100298411	100298412	G	C	46	GENIC	homozygous	52076775
9	100300461	100300463	TG	--	21	GENIC	homozygous	52076777
9	100304455	100304456	T	C	42	GENIC	possibly homozygous	52076779
9	100306790	100306791	G	GT	17	GENIC	homozygous	52076781
9	100308421	100308422	T	C	45	GENIC	heterozygous	52076783
9	100310231	100310232	T	TTTTTG	18	GENIC	homozygous	52076785