chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	210721644	210721645	A	G	66	GENIC	possibly homozygous	110908822
2	210721800	210721801	A	G	47	GENIC	homozygous	111420989
2	210721925	210721926	A	G	36	GENIC	homozygous	111420990
2	210721930	210721931	A	C	36	GENIC	homozygous	110908823
2	210721934	210721935	A	G	40	GENIC	homozygous	121707742
2	210721981	210721982	C	T	35	GENIC	possibly homozygous	110908824
2	210722031	210722032	A	G	39	GENIC	possibly homozygous	110908825
2	210722091	210722092	G	A	50	GENIC	possibly homozygous	111420991
2	210722603	210722604	A	G	53	GENIC	homozygous	111420992
2	210724058	210724059	G	A	55	GENIC	homozygous	110908827
2	210724842	210724843	C	G	51	GENIC	homozygous	110908829
2	210724941	210724942	G	A	57	GENIC	homozygous	110908830
2	210724965	210724966	C	T	58	GENIC	homozygous	111420993
2	210725060	210725061	A	G	51	GENIC	homozygous	110908832
2	210725406	210725407	A	G	43	GENIC	homozygous	110908833
2	210725623	210725624	C	G	47	GENIC	homozygous	110908834
2	210725648	210725649	G	A	43	GENIC	homozygous	111420994
2	210725649	210725650	G	A	42	GENIC	homozygous	111420995
2	210725656	210725657	A	G	44	GENIC	homozygous	110908835
2	210725973	210725974	A	G	10	GENIC	homozygous	110908836
2	210722988	210722988		TTTTCTTTTTC	37	GENIC	homozygous	131811578
2	210723024	210723030	CTGTAG		47	GENIC	homozygous	131811579
2	210726004	210726005	G	A	4	GENIC	heterozygous	131834953
2	210726010	210726011	A	G	10	GENIC	homozygous	132035304
2	210726014	210726015	A	G	4	GENIC	heterozygous	132035305