chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	211885639	211885640	T	A	13	GENIC	homozygous	59378973
2	211886313	211886314	C	CGTCGT	9	GENIC	homozygous	59378975
2	211886325	211886326	G	T	13	GENIC	homozygous	59378977
2	211886331	211886332	T	A	11	GENIC	homozygous	59378979
2	211886531	211886532	C	T	11	GENIC	homozygous	59378981
2	211887907	211887908	A	C	9	GENIC	homozygous	59378991
2	211886846	211886847	A	ATTATTT	13	GENIC	homozygous	62429257
2	211886722	211886723	T	A	8	GENIC	homozygous	59378983
2	211886805	211886806	G	GCAC	10	GENIC	homozygous	59378985
2	211888053	211888054	C	T	8	GENIC	homozygous	59378993
2	211889271	211889272	T	G	14	GENIC	homozygous	59378995
2	211889335	211889336	T	C	13	GENIC	homozygous	59378997
2	211889921	211889922	G	T	13	GENIC	homozygous	59378999
2	211891097	211891098	C	T	9	GENIC	homozygous	59379001
2	211891219	211891220	G	C	12	GENIC	homozygous	59379003
2	211892259	211892260	T	G	12	GENIC	homozygous	59379007
2	211892576	211892577	T	G	12	GENIC	homozygous	59379009
2	211893528	211893529	A	T	10	GENIC	homozygous	59379013
2	211893560	211893561	T	A	10	GENIC	homozygous	59379015
2	211893690	211893691	T	C	12	GENIC	homozygous	59379025