chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	170383693	170383694	C	G	42	INTERGENIC	homozygous	60940682
1	170383953	170383954	A	AGACT	29	INTERGENIC	homozygous	60940683
1	170384180	170384181	C	A	22	INTERGENIC	homozygous	60940684
1	170384360	170384361	G	A	33	GENIC	homozygous	61908990
1	170384559	170384560	T	C	29	GENIC	homozygous	60940685
1	170384771	170384772	C	T	26	GENIC	homozygous	61908991
1	170385213	170385218	CCTCC	-----	30	GENIC	homozygous	60940686
1	170385250	170385251	C	CGTGTGT	11	GENIC	heterozygous	61554220
1	170385289	170385291	AA	--	30	GENIC	heterozygous	62173148
1	170385292	170385293	T	TGTGTGTG	29	GENIC	heterozygous	62173150
1	170385294	170385295	C	-	28	GENIC	heterozygous	62173152
1	170385298	170385299	A	-	27	GENIC	heterozygous	62173154
1	170385374	170385375	A	T	20	GENIC	homozygous	61908992
1	170386312	170386313	A	AG	33	GENIC	homozygous	61908994
1	170386698	170386699	G	A	30	GENIC	homozygous	60940690
1	170386741	170386742	C	T	38	GENIC	homozygous	60940691
1	170387424	170387425	G	C	24	GENIC	homozygous	61908995