chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	170384559	170384560	T	C	45	GENIC	homozygous	60940685
1	170385213	170385218	CCTCC	-----	25	GENIC	homozygous	60940686
1	170385230	170385231	A	AC	19	GENIC	homozygous	60940687
1	170385251	170385253	GT	--	8	GENIC	homozygous	60940688
1	170386028	170386049	CAGCAGCAGCAGCAGCAGCAG	---------------------	10	GENIC	homozygous	61309747
1	170386072	170386073	G	A	27	GENIC	heterozygous	61309748
1	170386310	170386311	G	GAAA	36	GENIC	homozygous	60940689
1	170386698	170386699	G	A	56	GENIC	homozygous	60940690
1	170386741	170386742	C	T	55	GENIC	homozygous	60940691
1	170389522	170389523	G	T	40	GENIC	possibly homozygous	60940692
1	170395917	170395918	A	T	21	GENIC	heterozygous	60940693
1	170395922	170395923	T	A	24	GENIC	heterozygous	61309749
1	170395928	170395929	G	-	13	GENIC	heterozygous	60940694
1	170395957	170395958	T	A	30	GENIC	heterozygous	60940695
1	170396027	170396028	T	A	31	GENIC	heterozygous	60940696
1	170396042	170396043	A	T	27	GENIC	heterozygous	61309750
1	170396044	170396045	C	-	25	GENIC	homozygous	60940697
1	170396142	170396143	A	T	42	GENIC	heterozygous	61309751
1	170396232	170396233	A	T	28	GENIC	heterozygous	61309752
1	170400073	170400077	CTGT	----	33	GENIC	heterozygous	60940699
1	170400083	170400084	G	GTCTA	42	GENIC	heterozygous	61309753
1	170400088	170400092	TCTA	----	31	GENIC	possibly homozygous	60940700
1	170400163	170400171	CTATCTAT	--------	10	GENIC	homozygous	60940701
1	170401147	170401149	GT	--	41	GENIC	homozygous	60940702
1	170403127	170403128	A	AT	32	GENIC	heterozygous	60940703
1	170403531	170403535	CCTT	----	29	GENIC	homozygous	60940704
1	170403537	170403539	TT	--	39	GENIC	heterozygous	60940705
1	170403699	170403700	G	-	45	GENIC	heterozygous	61309754