chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	55341353	55341354	T	C	24	GENIC	homozygous	144820259
8	55341367	55341371	ACTT		28	GENIC	homozygous	145645762
8	55341467	55341468	A	C	27	GENIC	homozygous	144820260
8	55341683	55341684	T	A	29	GENIC	homozygous	145664877
8	55342350	55342351	G	T	32	GENIC	homozygous	145664878
8	55343008	55343009	G	A	20	GENIC	homozygous	145664879
8	55342013	55342014	A	C	30	GENIC	homozygous	138337132
8	55343463	55343464	A	C	27	GENIC	homozygous	145664880
8	55343499	55343500	G	A	26	GENIC	homozygous	145664881
8	55343527	55343528	A	G	26	GENIC	homozygous	145664882
8	55343542	55343543	A	G	25	GENIC	homozygous	138337134
8	55343966	55343967	T	C	37	GENIC	homozygous	145664883
8	55345186	55345187	T	C	31	GENIC	homozygous	138337135
8	55345383	55345384	T	C	19	GENIC	homozygous	145664884
8	55345719	55345720	C	T	17	GENIC	homozygous	138337136
8	55346081	55346081		CTC	16	GENIC	homozygous	145645763
8	55346491	55346492	C	T	17	GENIC	homozygous	145664885
8	55346531	55346532	G	C	19	GENIC	homozygous	145664886
8	55346826	55346827	A	G	18	GENIC	homozygous	145664887
8	55347221	55347222	A	G	23	GENIC	possibly homozygous	145664888