chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230167656	230167657	C	A	20	GENIC	homozygous	60084749
2	230167753	230167754	T	C	22	GENIC	homozygous	60084750
2	230168488	230168492	CTCC	----	16	GENIC	homozygous	61850704
2	230168834	230168835	T	C	24	GENIC	homozygous	60084752
2	230168926	230168927	C	T	30	GENIC	homozygous	60084753
2	230169016	230169017	G	A	19	GENIC	homozygous	60084754
2	230169402	230169403	A	G	22	GENIC	homozygous	60084755
2	230170260	230170261	G	GCT	15	GENIC	possibly homozygous	60084757
2	230170280	230170281	A	AC	13	GENIC	possibly homozygous	60084758
2	230170298	230170299	G	A	15	GENIC	homozygous	60084759
2	230171242	230171243	C	A	23	GENIC	homozygous	60084760
2	230171688	230171689	C	A	26	GENIC	homozygous	60084761
2	230171809	230171812	CTG	---	28	GENIC	homozygous	59431390