chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	100279101	100279102	G	C	24	GENIC	homozygous	52076743
9	100280091	100280092	A	G	24	GENIC	homozygous	52076745
9	100280951	100280952	T	-	18	GENIC	possibly homozygous	52076749
9	100281511	100281513	TT	--	1	GENIC	homozygous	53238807
9	100281889	100281890	T	TTAA	20	GENIC	homozygous	52076753
9	100282301	100282302	G	GA	17	GENIC	possibly homozygous	52076755
9	100282694	100282695	A	G	28	GENIC	homozygous	52076757
9	100283028	100283029	A	AGT	17	GENIC	heterozygous	52076759
9	100283029	100283031	GT	--	17	GENIC	heterozygous	52917234
9	100284478	100284479	C	CATGAGACACT	40	GENIC	homozygous	52076761
9	100291661	100291662	A	C	34	GENIC	homozygous	52076763
9	100291755	100291756	C	A	39	GENIC	homozygous	52076765
9	100291972	100291973	A	T	28	GENIC	homozygous	52076767
9	100294232	100294233	C	-	28	GENIC	homozygous	52076769
9	100297159	100297162	ACT	---	17	GENIC	homozygous	52076771
9	100297165	100297197	AAATGTTAAATATGTTAAATGTTAAATGTTAA	--------------------------------	23	GENIC	homozygous	52076773
9	100298411	100298412	G	C	38	GENIC	homozygous	52076775
9	100300461	100300463	TG	--	35	GENIC	homozygous	52076777
9	100304455	100304456	T	C	34	GENIC	homozygous	52076779
9	100308406	100308407	T	-	12	GENIC	heterozygous	52283697
9	100310231	100310232	T	TTTTTG	18	GENIC	homozygous	52076785