chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	114477083	114477084	C	A	21	GENIC	homozygous	114949803
6	114477102	114477103	C	T	21	GENIC	homozygous	118798206
6	114478217	114478218	T	C	21	GENIC	homozygous	118798207
6	114478248	114478249	G	A	24	GENIC	homozygous	118798208
6	114478392	114478393	C	T	22	GENIC	possibly homozygous	118798209
6	114478424	114478425	C	T	23	GENIC	possibly homozygous	118798210
6	114478678	114478679	A	G	16	GENIC	homozygous	118798211
6	114479008	114479009	T	C	21	GENIC	homozygous	118798212
6	114479153	114479154	A	C	19	GENIC	homozygous	118798213
6	114479331	114479332	A	G	22	GENIC	homozygous	118798214
6	114479878	114479879	T	A	27	GENIC	homozygous	118798215
6	114479882	114479883	A	G	27	GENIC	homozygous	114949807
6	114479892	114479893	A	T	26	GENIC	homozygous	118798216
6	114479906	114479907	A	G	25	GENIC	homozygous	114949808
6	114480777	114480781	TGTC		19	GENIC	homozygous	135112657
6	114478595	114478595		A	14	GENIC	homozygous	135112654
6	114479133	114479134	A		20	GENIC	homozygous	135112655
6	114479312	114479315	TCA		22	GENIC	homozygous	135112656
6	114482354	114482355	T	C	16	GENIC	homozygous	114949814
6	114482780	114482785	GATCT		19	GENIC	homozygous	135112658
6	114483870	114483871	A	G	16	GENIC	homozygous	114949818
6	114484697	114484697		T	21	GENIC	possibly homozygous	135112659
6	114488087	114488090	CGT		7	GENIC	homozygous	135112660
6	114488143	114488144	T	C	7	GENIC	homozygous	118798217
6	114489441	114489441		G	10	GENIC	possibly homozygous	135112661