chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	218654564	218654565	C	T	52	GENIC	homozygous	59937460
2	218654674	218654678	GTGT	----	33	GENIC	homozygous	59398953
2	218654695	218654696	T	C	40	GENIC	heterozygous	60082973
2	218654698	218654700	GC	--	37	GENIC	homozygous	59398954
2	218654802	218654803	C	T	55	GENIC	possibly homozygous	59937461
2	218654928	218654929	T	C	39	GENIC	homozygous	59398955
2	218655846	218655847	A	C	37	GENIC	homozygous	59398956
2	218656573	218656574	A	C	25	GENIC	homozygous	59937462
2	218656725	218656726	A	ATG	31	GENIC	possibly homozygous	59398957
2	218656822	218656823	A	G	54	GENIC	possibly homozygous	59398958
2	218656911	218656913	TG	--	27	GENIC	homozygous	59398959
2	218656935	218656937	TG	--	28	GENIC	homozygous	59398960
2	218657006	218657007	C	CTG	38	GENIC	possibly homozygous	59398961
2	218657675	218657676	G	-	6	GENIC	heterozygous	59937463