chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	211885639	211885640	T	A	27	GENIC	homozygous	59378973
2	211886313	211886314	C	CGTCGT	39	GENIC	homozygous	59378975
2	211886325	211886326	G	T	32	GENIC	homozygous	59378977
2	211886331	211886332	T	A	31	GENIC	homozygous	59378979
2	211886531	211886532	C	T	20	GENIC	homozygous	59378981
2	211887648	211887649	A	G	9	GENIC	homozygous	59378989
2	211886722	211886723	T	A	19	GENIC	homozygous	59378983
2	211886805	211886806	G	GCAC	5	GENIC	homozygous	59378985
2	211886846	211886847	A	T	2	GENIC	heterozygous	59378987
2	211887907	211887908	A	C	18	GENIC	homozygous	59378991
2	211888053	211888054	C	T	21	GENIC	homozygous	59378993
2	211889271	211889272	T	G	5	GENIC	homozygous	59378995
2	211889335	211889336	T	C	5	GENIC	homozygous	59378997
2	211889921	211889922	G	T	26	GENIC	homozygous	59378999
2	211891097	211891098	C	T	21	GENIC	homozygous	59379001
2	211891219	211891220	G	C	16	GENIC	homozygous	59379003
2	211892003	211892004	A	C	41	GENIC	homozygous	59379005
2	211892259	211892260	T	G	25	GENIC	homozygous	59379007
2	211892576	211892577	T	G	26	GENIC	homozygous	59379009
2	211893528	211893529	A	T	6	GENIC	homozygous	59379013
2	211893560	211893561	T	A	10	GENIC	homozygous	59379015
2	211893648	211893655	TTGTTTG	-------	8	GENIC	homozygous	59379017
2	211893650	211893655	GTTTG	-----	7	GENIC	heterozygous	59379019
2	211893650	211893651	G	-	7	GENIC	heterozygous	59379021
2	211893652	211893655	TTG	---	8	GENIC	heterozygous	59379023
2	211893690	211893691	T	C	16	GENIC	possibly homozygous	59379025